Page

1 Introduction

1.1 Objectives

1.2 Terminology

2 Overview of the method for deriving soil quality guidelines

2.1 Precision of estimates and rounding of added contaminant limits

3 Zinc

3.1 Zinc compounds considered

3.2 Exposure pathway assessment

3.3 Toxicity data

3.4 Normalisation relationships

3.5 Sensitivity of organisms to zinc

3.6 Calculation of soil quality guidelines for fresh zinc contamination

3.6.1 Calculation of soil quality guidelines for fresh zinc contamination based on no observed effect concentration and 10% effect concentration toxicity data

3.6.1.1 Calculation of soil-specific added contaminant limits

3.6.1.2 Calculation of ambient background concentration values

3.6.1.3 Examples of soil quality guidelines for fresh zinc contamination based on no observed effect concentration and 10% effect concentration data

3.6.2 Calculation of soil quality guidelines based on protecting aquatic ecosystems from leaching of fresh zinc contamination

3.6.3 Calculation of soil quality guidelines for fresh zinc contamination based on lowest observed effect concentration and 30% effect concentration toxicity data, and based on 50% effect concentration toxicity data

3.6.3.1 Calculation of soil-specific added contaminant limits

3.6.3.2 Calculation of ambient background concentration values

3.6.3.3 Examples of soil quality guidelines for fresh zinc contamination based on lowest observed effect concentration and 30% effect concentration data, and based on 50% effect data

3.7 Calculation of soil quality guidelines for aged zinc contamination

3.7.1 Calculation of an ageing and leaching factor for zinc

3.7.2 Calculation of soil quality guidelines for aged zinc contamination based on no observed effect concentration and 10% effect concentration toxicity data

3.7.2.1 Calculation of added contaminant limits for aged zinc contamination based on no observed effect concentration and 10% effect concentration toxicity data

3.7.2.2 Calculation of ambient background concentration values

3.7.2.3 Examples of soil quality guidelines for Australian soils with aged zinc contamination based on no observed effect concentration and 10% effect concentration data

3.7.3 Calculation of soil quality guidelines for aged zinc contamination based on lowest observed effect concentration and 30% effect concentration toxicity data and based on 50% effect concentration toxicity data

3.7.3.1 Calculation of added contaminant limits for aged zinc contamination based on lowest observed effect concentration and 30% effect concentration and based on 50% effect concentration toxicity data

3.7.3.2 Calculation of ambient background concentrations

3.7.3.3 Examples of soil quality guidelines for Australian soils with aged zinc contamination based on lowest observed effect concentration and 30% effect concentration data, and based on 50% effect concentration toxicity data

3.8 Reliability of the zinc soil quality guidelines

3.9 Comparison with other guidelines

4 Arsenic

4.1 Arsenic compounds considered

4.2 Exposure pathway assessment

4.3 Toxicity data

4.4 Normalisation relationships

4.5 Sensitivity of organisms to arsenic

4.6 Calculation of soil quality guidelines for fresh arsenic contamination

4.6.1 Calculation of soil quality guidelines for fresh arsenic contamination based on no observed effect concentration and 10% effect concentration toxicity data

4.6.1.1 Calculation of ambient background concentration values

4.6.2 Calculation of soil quality guidelines for fresh arsenic contamination based on protecting aquatic ecosystems from leaching

4.6.3 Calculation of soil quality guidelines for fresh arsenic contamination based on lowest observed effect concentration and 30% effect concentration toxicity data, and based on 50% effect concentration toxicity data

4.7 Calculation of soil quality guidelines for aged arsenic contamination

4.7.1 Calculation of an ageing and leaching factor for arsenic

4.7.2 Calculation of soil quality guidelines for aged arsenic contamination

4.7.3 Calculation of ambient background concentration values

4.8 Reliability of the soil quality guidelines

4.9 Comparison with other guidelines

5 Naphthalene

5.1 Compounds considered

5.2 Exposure pathway assessment

5.3 Toxicity data

5.4 Normalisation relationships

5.5 Sensitivity of organisms to naphthalene

5.6 Calculation of soil quality guidelines for fresh naphthalene contamination

5.6.1 Calculation of soil quality guidelines for fresh naphthalene contamination based on no observed effect concentration and 10% effect concentration toxicity data

5.6.1.1 Calculation of ambient background concentration values

5.6.2 Calculation of soil quality guidelines for fresh naphthalene contamination based on lowest observed effect concentration and 30% effect concentration data, and based on 50% effect concentration toxicity data

5.7 Calculation of soil quality guidelines for aged naphthalene contamination

5.8 Metabolites of naphthalene

5.9 Reliability of the soil quality guidelines

5.10 Comparison with other guidelines

6 DDT

6.1 Compounds considered

6.2 Pathway risk assessment

6.3 Toxicity data

6.4 Normalisation relationships

6.5 Sensitivity of organisms to DDT

6.6 Calculation of soil quality guidelines for fresh DDT contamination

6.6.1 Calculation of generic soil quality guidelines for fresh DDT contamination based on no observed effect concentration and 10% effect concentration toxicity data

6.6.2 Calculation of soil quality guidelines for fresh DDT contamination based on lowest observed effect concentration data and 30% effect concentration data, and based on 50% effect concentration toxicity data

6.7 Calculation of soil quality guidelines for aged contamination

6.8 Reliability of soil quality guidelines

6.9 Important metabolites of DDT

6.10 Comparison with other guidelines

7 Copper

7.1 Copper compounds considered

7.2 Exposure pathway assessment

7.3 Toxicity data

7.4 Normalisation relationships

7.5 Sensitivity of organisms to copper

7.6 Calculation of soil quality guidelines for fresh copper contamination

7.6.1 Calculation of soil quality guidelines for fresh copper contamination based on no observed effect concentration and 10% effect concentration toxicity data

7.6.1.1 Calculation of soil-specific added contaminant limits

7.6.1.2 Calculation of ambient background concentration values

7.6.1.3 Examples of soil quality guidelines for fresh copper contamination based on no observed effect concentration and 10% effect concentration data

7.6.2 Calculation of soil quality guidelines for fresh copper contamination based on lowest observed effect concentration and 30% effect concentration toxicity data, and on 50% effect concentration data

7.6.2.1 Calculation of soil-specific added contaminant limits

7.6.2.2 Calculation of ambient background concentration values

7.6.2.3 Examples of soil quality guidelines for fresh copper contamination in Australian soils based on lowest observed effect concentration and 30% effect concentration toxicity data, and on 50% effect concentration data.

7.7 Calculation of soil quality guidelines for aged copper contamination

7.7.1 Calculation of an ageing and leaching factor for copper

7.7.2 Calculation of soil quality guidelines for aged copper contamination based on no observed effect concentration and 10% effect concentration toxicity data

7.7.2.1 Calculation of soil-specific added contaminant limits

7.7.2.2 Calculation of ambient background concentration values

7.7.2.3 Examples of soil quality guidelines for aged copper contamination in Australian soils based on no observed effect concentration and 10% effect concentration data.

7.7.3 Calculation of soil quality guidelines for aged copper contamination based on LOEC and 30% effect concentration toxicity data, and on 50% effect concentration data.

7.7.3.1 Calculation of soil-specific added contaminant limits

7.7.3.2 Calculation of ambient background concentration values

7.7.3.3 Examples of soil quality guidelines for aged copper contamination in Australian soils based on lowest observed effect concentration and 30% effect concentration data

7.8 Reliability of the soil quality guidelines

7.9 Comparison with other guidelines

8 Lead

8.1 Lead compounds considered

8.2 Exposure pathway assessment

8.3 Toxicity data

8.4 Normalisation relationships

8.5 Sensitivity of organisms to lead

8.6 Calculation of soil quality guidelines for fresh lead contamination

8.6.1 Calculation of soil quality guidelines for fresh lead contamination based on NOEC and 10% effect concentration toxicity data

8.6.1.1 Calculation of soil-specific added contaminant limits

8.6.1.2 Calculation of ambient background concentration values

8.6.1.3 Examples of soil quality guidelines for fresh lead contamination in Australian soils based on no observed effect concentration and 10% effect concentration data

8.6.2 Calculation of soil quality guidelines for fresh lead contamination based on LOEC and 30% effect concentration toxicity data and on 50% effect concentration data

8.6.2.1 Calculation of soil-specific added contaminant limits

8.6.2.2 Calculation of ambient background concentration values

8.6.2.3 Examples of soil quality guidelines for fresh lead contamination in Australian soils based on lowest observed effect concentration and 30% effect concentration data and on 50% effect concentration data

8.7 Calculation of soil quality guidelines for aged lead contamination

8.7.1 Calculation of an ageing and leaching factor

8.7.2 Calculation of soil quality guidelines for aged lead contamination based on NOEC and 10% effect concentration toxicity data

8.7.2.1 Calculation of soil-specific added contaminant limits

8.7.2.2 Calculation of ambient background concentration values

8.7.2.3 Examples of soil quality guidelines for aged lead contamination in Australian soils based on no observed effect concentration and 10% effect concentration data.

8.7.3 Calculation of soil quality guidelines for aged lead contamination based on LOEC and 30% effect concentration toxicity data and on 50% effect concentration data

8.7.3.1 Calculation of added contaminant limits

8.7.3.2 Calculation of ambient background concentration values

8.7.3.3 Examples of soil quality guidelines for aged lead contamination in Australian soils based on lowest observed effect concentration and 10% effect concentration data and on 50% effect concentration data.

8.8 Reliability of the soil quality guidelines

8.9 Comparison with other guidelines

9 Nickel

9.1 Nickel compounds considered

9.2 Exposure pathway assessment

9.3 Toxicity data

9.4 Normalisation relationships

9.5 Sensitivity of organisms to nickel

9.6 Calculation of soil quality guidelines for fresh nickel contamination

9.6.1 Calculation of soil quality guidelines for fresh nickel contamination based on no observed effect concentration and 10% effect concentration toxicity data

9.6.1.1 Calculation of soil-specific added contaminant limits

9.6.1.2 Calculation of ambient background concentration values

9.6.1.3 Examples of soil quality guidelines for fresh nickel contamination in Australian soils based on no observed effect concentration and 10% effect concentration data

9.6.2 Calculation of soil quality guidelines for fresh nickel contamination based on LOEC and 30% effect concentration toxicity data, and on 50% effect concentration data

9.6.2.1 Calculation of soil-specific added contaminant limits

9.6.2.2 Calculation of ambient background concentration values

9.6.2.3 Examples of soil quality guidelines for fresh nickel contamination in Australian soils based on lowest observed effect concentration and 30% effect concentration data, and based on 50% data

9.7 Calculation of soil quality guidelines for aged nickel contamination

9.7.1 Calculation of ageing and leaching factors for nickel

9.7.2 Use of ageing and leaching factors in the methodology

9.7.3 Calculation of soil quality guidelines for aged nickel contamination based NOEC and 10% effect concentration toxicity data

9.7.3.1 Calculation of soil-specific added contaminant limits

9.7.3.2 Calculation of ambient background concentration values

9.7.3.3 Examples of soil quality guidelines for aged nickel contamination in Australian soils based on no observed effect concentration and 10% effect concentration data

9.7.4 Calculation of soil quality guidelines for aged nickel contamination based on LOEC and 30% effect concentration toxicity data, and on 50% effect concentration data

9.7.4.1 Calculation of soil-specific added contaminant limits

9.7.4.2 Calculation of ambient background concentration values

9.7.4.3 Examples of soil quality guidelines for fresh nickel contamination in Australian soils based on lowest observed effect concentration and 30% effect concentration data, and based on 50% effect concentration data

9.8 Reliability of the soil quality guidelines

9.9 Comparison with other guidelines

10 Trivalent chromium

10.1 Chromium (III) compounds considered

10.2 Exposure pathway assessment

10.3 Toxicity data

10.4 Normalisation relationships

10.5 Sensitivity of organisms to trivalent chromium

10.6 Calculation of soil quality guidelines for fresh trivalent chromium contamination

10.6.1 Calculation of added contaminant limits for fresh trivalent chromium contamination

10.6.2 Calculation of ambient background concentration values for fresh trivalent chromium contamination

10.6.3 Examples of soil quality guidelines for fresh trivalent chromium contamination in Australian soils

10.7 Calculation of soil quality guidelines for aged trivalent chromium contamination

10.7.1 Calculation of an ageing and leaching factor for trivalent chromium

10.7.2 Calculation of added contaminant limits for aged trivalent chromium contamination

10.7.3 Calculation of ambient background concentration values

10.7.4 Examples of soil quality guidelines for aged trivalent chromium contamination in Australian soils

10.8 Reliability of the soil quality guidelines

10.9 Comparison with other guidelines

11 Summary

12 Bibliography

13 Appendices

13.1 Appendix A: Raw toxicity data for zinc

13.2 Appendix B. Raw toxicity data for arsenic

13.3 Appendix C: Raw toxicity data for naphthalene

13.4 Appendix D: Raw toxicity data for DDT

13.5 Appendix E: Raw toxicity data for copper

13.6 Appendix F: Explanation of the selection of the soil properties that control the added contaminant limits for copper

13.7 Appendix G. Raw toxicity data for lead

13.8 Appendix H: Raw toxicity data for nickel

13.9 Appendix I: Raw toxicity data for trivalent chromium

14 Glossary

15 Shortened forms

 

1                   Introduction

The objective of this guideline is to derive EILs for arsenic (As), copper (Cu), chromium III (Cr (III)), dichlorodiphenyltrichloroethane (DDT), naphthalene, nickel (Ni), lead (Pb) and zinc (Zn) using the methodology detailed in Schedule B5b to:

The term ‘soil quality guideline’ (SQG) is used in this guideline to describe any concentration-based limit for contaminants in soils.

 

A combination of lowest observed effect concentration (LOEC) and 30% effect concentration data (EC30) has been adopted in the NEPM for the derivation of EILs. Equivalent data for EC10 and EC50 is included for information purposes only.

2                   Overview of the method for deriving soil quality guidelines

Soil quality guidelines can have various purposes. The National Environment Protection (Assessment of Site Contamination) Measure (NEPM) contains a specific type of SQG, the ecological investigation level (EIL), to guide the assessment of contaminated sites in Australia. The EILs were derived in such a manner that when they are exceeded it indicates that terrestrial ecosystems may experience harmful effects due to the presence of contaminants. The EILs are thus used to indicate when further investigation is necessary.

 

However, SQGs with other purposes can and have been developed. For example, the Dutch have three sets of SQGs, each with a different purpose. These are target levels (their purpose is to indicate the long-term goals for the concentration of contaminants), maximum permissible levels (their purpose is to define the maximum level of contamination that is considered acceptable), and intervention levels (their purpose is to define the maximum permitted concentration before some immediate action is required).

 

As a result of consultation conducted in developing the Australian methodology in November 2008, three different sets of ecotoxicity data were used to derive SQGs. The three sets of SQGs are termed SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) reflecting the type of ecotoxicity data that was used in their generation. A summary of the three types of SQGs, the data used and likely ecotoxicological effects that would be expected to occur if these are met is presented in Table 1. A combination of lowest observed effect concentration (LOEC) and 30% effect concentration data (EC30) has been adopted in the NEPM for the derivation of EILs.

Table 1. The relationship between the three types of soil quality guidelines (SQGs), the data that is used to derive the SQGs and the type of toxic effects that would be experienced if the SQGs are met.

Type of SQG

Toxicity data used to calculate the SQGs

Expected toxic effects if the SQG is not exceeded

SQG(NOEC & EC10)

NOEC and EC10

slight toxic effects

SQG(LOEC & EC30)

LOEC and EC30

moderate toxic effects

SQG(EC50)

EC50

significant toxic effects

 

An overview of the SQG derivation methodology (detailed in Schedule B5b) is presented in Figure 1. One of the key aims in developing the methodology was to account for the availability and toxicity of the contaminant in the soil being studied. To do this, key soil and site-specific factors that are known to modify the toxicity of contaminants had to be accounted for. One factor that was incorporated into the methodology was the background concentration. In order to do this, the data used to derive the SQGs was expressed in terms of the amount of contaminant that had to be added to the soil to cause toxicity. When this toxicity data was used in accordance with the methodology, the resulting value was termed the added contaminant level (ACL). An ambient background concentration (ABC) specific to the soil being investigated was then added to the ACL to calculate the SQG.

 

ACL values are generated as part of the methodology of deriving SQGs. Thus, it is necessary to differentiate the ACLs generated in deriving SQG(NOEC & EC10) from those generated in deriving SQG(LOEC & EC30) and SQG (EC50) values. The ACL generated in deriving an SQG(NOEC & EC10) is termed the NOEC and EC10-based ACL (ACL(NOEC & EC10)). Similarly, ACLs generated in deriving SQG(LOEC & EC30) and SQG (EC50) values are referred to as the LOEC and EC30-based ACL (ACL(LOEC & EC30)) and the EC50-based ACL (ACL(EC50)).

 

 

Figure 1. Overview of the  methodology for deriving soil quality guidelines based on NOEC and EC10 data (SQG(NOEC & EC10)) indicated by the green (far left) arrows, based on LOEC and EC30 data (SQG(LOEC & EC30)) indicated by the orange (middle) arrows and based on EC50 data (SQG(EC50)) indicated by the red (far right) arrows. As part of this process, ACLs and ABCs are calculated. The differences between the three SQGs are presented in Table 1.

The key steps in the methodology are:

  1. determining the purpose of the SQG and the appropriate level of protection
  2. determining the most important exposure pathways
  3. collating and screening the toxicity data
  4. determining whether the contamination is fresh or aged and whether there are ageing/leaching factors available to account for this
  5. normalising the toxicity data
  6. calculating the ACL
  7. accounting for biomagnification
  8. measuring or calculating the ABC
  9. calculating SQG(NOEC & EC10),  SQG(LOEC & EC30) and SQG(EC50) values for fresh contamination in soils with different land uses
  10. calculating SQG(NOEC & EC10),  SQG(LOEC & EC30) and SQG(EC50) values for aged contamination in soils with different land uses.

These key steps and the decision pathway involved in deriving ACL(NOEC & EC10) and SQG(NOEC & EC10) values are provided in Figure 2 below. Exactly the same procedure would be used to derive SQG(LOEC & EC30) and SQG(EC50) values, except that different toxicity data would be used (Table 1). Details of the methodology for calculating SQGs are provided in Schedule B5b.

 

Land has a variety of potential uses, and the level of protection that is appropriate for each land use varies. For example, it is appropriate for a higher level of protection to be applied to areas of ecological significance compared to industrial land. The recommended levels of protection for various land uses are provided in Schedule B5b and are used in this guideline.  For contaminants that do not biomagnify, the recommended level of protection of species for areas of ecological significance, urban residential/public open space and commercial/industrial land are 99%, 80% and 60% respectively. For contaminants that biomagnify, the recommended levels of protection of species for areas of ecological significance, urban residential/public open space and commercial/industrial land are 99%, 85% and 65% respectively. SQGs were generated for areas of ecological significance, urban residential land/public open space, and commercial/industrial land uses.

 

The contamination at many contaminated sites is not fresh, rather it has been there for some years. The biological availability (bioavailability) and toxicity of many contaminants decreases over time (that is, it ages) due to binding to soil particles, chemical and biological degradation and a range of other processes. Furthermore, in many laboratory-based ecotoxicity experiments that spike soils with soluble metal salts, ecotoxicity is overestimated due to a lack of leaching of soluble salts which affect metal sorption. These factors have been addressed in recent risk assessments for metals in soils using ’ageing/leaching‘ factors, and can be accounted for by multiplying the toxicity data by an ageing/leaching factor and thus deriving SQGs for aged contamination. Site-specific assessments of a contaminants bioavailability can also be made, but these are usually conducted as part of a more detailed site-specific (Tier 2) ecological risk assessment. When ageing/leaching factors were available for the test chemicals examined in this study, SQGs were derived for aged contamination.

 

When contaminants are introduced to soil, some will bind strongly to the soil while others are mobile and will move off-site. Leaching to groundwater is a key off-site migration pathway and can result in aquatic ecosystems being exposed to contaminants. Therefore, the potential of contaminants to leach is an important characteristic that affects the environmental fate and effect they cause. The leaching potential is not controlled solely by the physicochemical properties of contaminants, but also by the properties of the soil containing the contaminant and climatic conditions. It is not possible or appropriate to account for the potential to leach in deriving practical SQGs at a generic level, rather this should be done as part of a more detailed site-specific ecological risk assessment.

 

Given the available data, the most complete set of SQGs was derived for each of the eight contaminants. A summary of what SQGs could be derived is presented below.

 

In addition, SQGs that account for the potential of contaminants to leach (and therefore should protect aquatic ecosystems) were derived for arsenic and zinc. This was only done for these contaminants to illustrate how this is done and what effect it has on the resulting SQGs compared to the SQGs that do not account for leaching.

In order to increase the readability and ease of use of this report the ACL, ABC and SQG values presented in the various tables have all been rounded off using the following scheme:

Figure 2. Schematic of the methodology for deriving soil quality guidelines (SQGs) (modified from Heemsbergen et al. 2008). Green arrows show the path when the preceding question was answered with a ‘yes’ while the red arrows indicate the path when the answer was ‘no’. Blue arrows indicate the path when there is no choice.

3                   Zinc

The SQGs for Zn were derived using data for the following:

The two key considerations in determining the most important exposure pathways for inorganic contaminants are whether they biomagnify (see Glossary) and whether they have the potential to leach to groundwater.

 

A surrogate measure of the potential for a contaminant to leach is its watersoil partition coefficient (Kd). If the logarithm of the Kd (log Kd) of an inorganic contaminant is less than 3 then it is considered to have the potential to leach to groundwater (Schedule B5b). The Australian National Biosolids Research Program (NBRP) measured the log Kd of Zn in 17 agricultural soils throughout Australia. These measurements showed that in most soils the log Kd of Zn was below 3 L/kg (unpublished data). The log Kd value for Zn reported by Crommentuijn et al. (2000) was 2.2 L/kg. Therefore, there is the potential for Zn in some soils to leach to groundwater and affect aquatic ecosystems. However, the methodology for EIL derivation (Schedule B5b) does not advocate the routine derivation of EILs that account for leaching potential. Rather, it advocates that this is done on a site-specific basis as appropriate. However, the calculations of Zn SQGs that account for leaching have been included here as an illustration of the process and the effect that this has on the resulting soil quality guidelines.

 

Zinc is an essential element and, as such, concentrations of Zn in tissue are highly regulated and it does not biomagnify (Louma & Rainbow 2008; Schedule B5b). Therefore, the biomagnification route of exposure does not need to be considered for Zn and the SQGs will only account for direct toxicity.

Zinc is a well-studied inorganic contaminant and therefore a large dataset of toxicity values was available. Most studies presented their toxicity data in terms of added concentration (that is, the concentration of the contaminant added to the soil that causes a specified toxic effect) and so could be used without further modification. Some toxicity data was expressed in terms of total contaminant concentration but the background concentrations were reported. In such cases, the toxicity data was converted to an added concentration basis by subtracting the background from the total concentration. If toxicity data was expressed in terms of total contaminant concentration but the background concentration was not reported then the Dutch background correction equation (Lexmond et al. 1986) was used to estimate the background concentration.

 

background Zn = 1.5 * [2 * organic matter (%) + clay content (%)]  (equation 1)

 

The background concentration was then subtracted from the total concentration data to derive the added concentration toxicity value.

 

The toxicity database used to calculate the SQG(NOEC & EC10) values for Zn included EC10 and NOEC toxicity data for nine soil processes (Table 2), 14 invertebrate species and 1 invertebrate community measurement (Table 3) and 22 plant species (Table 4). The raw data used to generate Tables 24 is provided in Appendix A. There was sufficient data (that is, toxicity data) for at least five species or soil processes that belong to at least three taxonomic or nutrient groups (Schedule B5b) available to derive SQG(NOEC & EC10) values using a species sensitivity distribution (SSD) methodology. Given that Zn does not biomagnify, the level of protection recommended for non-biomagnifying contaminants was used to generate the SQG for each land use.

 

Table 2. The geometric mean values of the zinc toxicity data (expressed in terms of added Zn) for individual soil processes.

Soil process

Geometric means (mg/kg added Zn)

 

EC10 or NOEC

EC30 or LOEC

EC50

Acetate decomposition

187

280

560

Amidase

121

182

364

Ammonification

98

148

295

Arylsulphatase

289

434

868

Glucose decomposition

274

1169

2904

Nitrate reductase

56

84

168

Nitrification

455

706

930

Phosphatase

674

1011

2022

Respiration

104

157

313

Table 3. The geometric mean values of zinc (Zn) toxicity data (as added Zn) for soil invertebrate species and an invertebrate community.

Species/endpoint

Geometric means (mg/kg added Zn)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Earthworm

Aporrectodea caliginosa

223

274

391

Earthworm

Aporrectodea rosea

390

407

436

Earthworm

Eisenia fetida

201

296

575

Earthworm

Lumbriculus rubellus

220

285

443

Earthworm

Lumbriculus terrestris

1062

1257

1675

Nematode

Acrobeloides sp.

221

332

663

Nematode

Caenorhabditis elegans

122

183

366

Nematode

C. elegans (dauer larvae)

689

1034

2068

Nematode

Community nematodes

306

459

919

Nematode

Eucephalobus sp.

135

202

403

Nematode

Plectus sp.

23

35

70

Nematode

Rhabditidae sp.

199

299

597

Potworm

Enchytraeus albidus

121

181

363

Potworm

Enchytraeus crypticus

276

414

828

Springtail

Folsomia candida

188

283

565

 

Table 4. The geometric mean values of the zinc (Zn) toxicity data (expressed in terms of added Zn) for individual plant species.

Plant species

Geometric means (mg/kg added Zn)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Alfalfa

Medicago sativa

198

297

595

Barley

Hordeum vulgare

83

233

495

Beet

Beta vulgaris

198

297

595

Black or white lentil

Vigna mungo

95

142

284

Canola

Brassica napus

230

328

409

Common vetch

Vicia sativa

42

63

127

Cotton

Gossypium sp.

272

288

293

Fenugreek

Trigonella foenum graecum

106

159

318

Lettuce

Latuca sativa

264

396

793

Maize

Zea mays

202

304

581

Millet

Panicum milaceum

540

1580

2026

Oats

Avena sativa

222

333

667

Onion

Allium cepa

66

99

198

Pea

Pisum sativum

264

396

793

Peanuts

Arachis hypogaea

140

224

280

Red clover

Trifolium pratense

39

59

117

Sorghum

Sorghum sp.

123

254

444

Spinach

Spinacia oleracea

132

198

396

Sugar cane

Sacharum

3220

4830

9661

Tomato

Lycopersicon esculentum

264

396

793

Triticale

Tritosecale sp.

998

1364

1658

Wheat

Triticum aestivum

640

928

1172

 

A normalisation relationship is an empirical model that predicts the toxicity of a single contaminant to a single species using soil physicochemical properties (for example, soil pH and organic carbon content). Seven normalisation relationships were reported in the literature for Zn toxicity (Table 5). Three were developed for Australian soils (Broos et al. 2007; Warne et al. 2008a; Warne et al. 2008b) and four have been derived for European soils (Lock & Janssen 2001; Smolders et al. 2003). Three of the relationships were for plants, two for microbial functions and two for soil invertebrates. Of these, relationships 14, 6 and  7 were used to derive Zn SQGs. Relationship number 5 for wheat was not used, as an equivalent field-based relationship for Australian soils was available and field-based normalisation relationships provide better estimates of toxicity in the field (Warne et al. 2008a) and thus are preferred to laboratory-based relationships (Schedule B5b).

 

Normalisation relationships are used to account for the effect of soil characteristics on toxicity data, so the resulting toxicity data more closely reflect the inherent sensitivity of the test species. All the Zn toxicity data in Tables 2–4 was normalised to their equivalent toxicity in the recommended Australian reference soil (Schedule B5b) (Table 6). Depending on the conditions under which the toxicity tests were conducted, the normalised toxicity data could be higher or lower in the reference soil compared to the original toxicity data in the test soil.

 

Table 5. Normalisation relationships for the toxicity of zinc to soil invertebrates, soil processes and plants.

Eqn no.

Species/soil process

Y parameter

X parameter(s)

Reference

1

E. fetida

(earthworm)

log EC50

 

0.79 * log CEC

Lock and Janssen 2001

2

F. candida

(collembola)

log EC50

 

1.14 * log CEC

Lock and Janssen 2001

3

PNR

log EC50

0.15 * pH

Smolders et al. 2003

4

SIN

log EC50

0.34 * pH + 0.93

Broos et al. 2007

5

T. aestivum

(wheat)

log EC10

0.14 * pH + 0.89 * log OC + 1.67

Warne et al. 2008a

6

log EC10

0.271 * pH +0.702 * CEC + 0.477

Warne et al. 2008b

7

log EC50

0.12 * pH +0.89 * log CEC + 1.1

Smolders et al. 2003

CEC = cation exchange capacity (cmolc/kg); OC = organic carbon content (%); PNR = potential nitrification rate; SIN = substrate induced respiration.

 

Table 6. Values of soil characteristics for the recommended Australian reference soil to be used to normalise toxicity data

Soil property

Value

pH

6

Clay (%)

10

CEC (cmolc/kg)

10

OC (%)

1               

 

The toxicity data (geometric means) used by the SSD method to calculate the ACL is shown in Table 2 for soil processes, Table 3 for soil invertebrates and Table 4 for plants. Figure 3 shows the SSD (that is, a cumulative distribution of the geometric means of the species) for all species for which there was Zn toxicity data. Toxicity data for plants, soil processes and soil invertebrates was evenly spread in the SSD, which indicates that these groups of organisms all have a similar sensitivity to Zn. Therefore, all the toxicity data was used to derive the ACLs, thus increasing the quantity of data used in the SSD method and increasing the reliability of the ACL values.

Figure 3. The species sensitivity distribution (plotted as a cumulative frequency against added zinc (Zn) concentration) for soil processes, soil invertebrates and plant species to Zn.

 

Soil quality guidelines were derived for fresh zinc contamination using three different sets of toxicity data: NOEC and EC10; LOEC and EC30; and EC50. The methods by which they were calculated and the resulting ACL and SQG values are presented in the following sections.

The NOEC and EC10 toxicity data were normalised using the equations presented in Table 5 to the Australian reference soil (Table 6) and then the lowest geometric mean for each species/soil microbial process was entered into the BurrliOZ species sensitivity distribution (Campbell et al. 2000) method. The SSD generated a single numerical value (that is, the ACL(NOEC & EC10) for each desired level of protection. These ACL(NOEC & EC10) values only apply to the Australian reference soil.

 

The ACL(NOEC & EC10) value for the Australian reference soil with an urban residential land/public open space use was approximately 100 mg/kg. These ACL(NOEC & EC10) values for the reference soil were then used to calculate ACL(NOEC & EC10) values for a range of soils (that is, soil-specific ACL(NOEC & EC10)) for each group of organisms using the same normalisation relationships as before but in the reverse manner. The following explains how the soil-specific ACL(NOEC & EC10) values for soils with an urban residential /public open space land use were calculated as an example of how this was done for each of the land uses.

 

Soil-specific ACL(NOEC & EC10) values for soil processes varied with soil pH and ranged from 20 to 330 mg/kg added Zn for soils with pHs between 4 and 7.5 (Table 7). The soil-specific ACL(NOEC & EC10) values for invertebrates (Table 8) varied with cation exchange capacity (CEC), with values ranging from 60 to 420 mg/kg for soils with CEC values ranging from 5 to 60 cmolc/kg. Soil-specific ACL(NOEC & EC10) values for plants (Table 9) were pH- and CEC- specific and ranged from 20 to 910 mg/kg for soils with pHs between 4 and 7.5 and CEC values between 5 and 60 cmolc/kg.

 

Table 7. Soil-specific ACL values for zinc (Zn) based on no observed effect concentration and 10% effect concentration toxicity data that should theoretically protect 80% of soil processes in soils with pH values ranging from 4.0 to 7.5.

Soil pH

Zn ACL (mg/kg)

for soil processes

4.0

20

4.5

30

5.0

45

5.5

70

6.0

100

6.5

150

7.0

220

7.5

330

 

Table 8. Soil-specific ACL values for zinc (Zn) based on no observed effect concentration and 10% effect concentration toxicity data that should theoretically protect 80% of invertebrate species in soils with CEC ranging from 5 to 60 cmolc/kg.

Cation exchange capacity (cmolc/kg)

Zn ACL (mg/kg) for invertebrates

5

60

10

100

20

180

30

240

40

300

60

420

 

Table 9. Soil-specific ACL values for zinc (Zn) based on no observed effect concentration and 10% effect concentration toxicity data that should theoretically protect 80% of plant species in soils with pH values ranging from 4.0 to 7.5 and CEC values ranging from 5 to 60 cmolc/kg.

pH

CEC (cmolc/kg)

 

5

10

20

30

40

60

4.0

20

30

50

65

75

100

4.5

25

40

65

85

110

140

5.0

35

55

90

120

140

190

5.5

45

75

120

160

200

260

6.0

65

100

170

220

270

360

6.5

85

140

230

300

370

490

7.0

120

190

310

410

500

670

7.5

160

260

420

560

690

910

 

These soil-specific ACL(NOEC & EC10) values for each organism group (presented in Tables 7 to 9) were then merged into a single set of soil-specific ACL(NOEC & EC10) valuesso that the lowest ACL(NOEC & EC10) value for each combination of soil pH and CEC was adopted (Table 10). The ACL(NOEC & EC10) values presented in Table 10 should protect at least 80% of soil processes, soil invertebrate and plant species and these ranged from 20 to 330 mg/kg in soils with pH values between 4 and 7.5 and CEC values between 5 and 60 cmolc/kg. The ACL(NOEC & EC10) values presented in Tables 79 are the ACLs for individual groups of organisms and should not be used as ACL(NOEC & EC10) values.

 

Table 10. Soil-specific added contaminant limits based on no observed effect concentration and 10% effect concentration toxicity data (ACL(NOEC & EC10), mg/kg) for zinc (Zn) that theoretically protect at least 80% of soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and CEC values ranging from 5 to 60 cmolc/kg. These values may be used as ACLs(NOEC & EC10)  for Zn in freshly contaminated soils with an urban residential /public open space land use.

pH

CEC (cmolc/kg)

 

5

10

20

30

40

60

4.0

20

20

20

20

20

20

4.5

25

30

30

30

30

30

5.0

35

45

45

45

45

45

5.5

45

70

70

70

70

70

6.0

60

100

100

100

100

100

6.5

60

100

150

150

150

150

7.0

60

100

180

220

220

220

7.5

60

100

180

240

300

330

 

The same methods as described above were used to generate the ACL (NOEC & EC10) values for areas of ecological significance and commercial/industrial land uses. The ACL (NOEC & EC10) values for these land uses are presented in Tables 11 and 12.

Table 11. Soil-specific added contaminant limits based on no observed effect concentration and 10% effect concentration toxicity data (ACL(NOEC & EC10), mg/kg) for zinc (Zn) that theoretically protect at least 99% of soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and CEC values ranging from 5 to 60 cmolc/kg. These values may be used as ACLs(NOEC & EC10) for Zn in freshly contaminated soils for areas of ecological significance.

pH

CEC (cmolc/kg)

 

5

10

20

30

40

60

4.0

4

5

5

5

5

5

4.5

6

8

8

8

8

8

5.0

8

10

10

10

10

10

5.5

10

15

15

15

15

15

6.0

15

25

25

25

25

25

6.5

15

25

35

35

35

35

7.0

15

25

45

55

55

55

7.5

15

25

45

60

75

80

 

Table 12. Soil-specific added contaminant limits based on no observed effect concentration and 10% effect concentration toxicity data (ACL(NOEC & EC10), mg/kg) for zinc (Zn) that theoretically protect at least 60% of soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and cation exchange capacity (CEC) values ranging from 5 to 60 cmolc/kg. These values may be used as ACLs(NOEC & EC10) for Zn in freshly contaminated soils with a commercial/industrial land use.

pH

CEC (cmolc/kg)

 

5

10

20

30

40

60

4.0

30

35

35

35

35

35

4.5

40

50

50

50

50

50

5.0

55

75

75

75

75

75

5.5

75

110

110

110

110

110

6.0

95

160

160

160

160

160

6.5

95

160

240

240

240

240

7.0

95

160

280

350

350

350

7.5

95

160

280

390

480

520

 

To convert ACLs to SQGs, the ambient background concentration (ABC) needs to be added to the ACL. Three methods of determining the ABC were recommended in the methodology for deriving SQGs (Schedule B5b). The preferred method is to measure the ABC at an appropriate reference site. However, where this is not possible the methods of Olszowy et al. (1995) and Hamon et al. (2004) were recommended, depending on the situation.

 

For sites with no history of contamination the method of Hamon et al. (2004) was recommended to estimate the ABC. In this method, the ABC for Zn varies with the soil iron concentration (Table 13). Predicted ABC values for Zn range from 3 to 60 mg/kg in soils with iron concentrations between 0.1 and 20%.

 

Table 13. Zinc (Zn) ABC calculated using the Hamon et al. (2004) method.

Soil iron content (%)

Zn ABC (mg/kg)

0.1

3

1

10

10

40

20

60

 

For aged contaminated sites (i.e. the contamination has been in place for at least two years, see Schedule B5b) the methodology recommends using the 25th percentiles of the ABC data for the ‘old suburbs’ of Olszowy et al. (1995) (see Table 14). The ABC values for Zn in ‘new suburbs’ were similar to the values predicted by the Hamon et al. (2004) method. Therefore it is recommended that the Hamon et al. (2004) method be used to generate ABC values for new suburbs (that is, <2 years old) as soil-specific values will be generated, while for old suburbs with aged contamination (that is, >2 years) it was recommended that the 25th percentile of the ABC data from old suburbs (Olszowy et al. 1995) be used.

Table 14. Zinc (Zn) ABC based on the 25th percentiles of Zn concentrations in ‘old suburbs’ (i.e. >2 years old) from various states of Australia (Olszowy et al. 1995).

Suburb type

25th percentile of Zn ABC values (mg/kg)

 

NSW

QLD

SA

VIC

 

New suburb, low traffic

25

15

25

15

New suburb, high traffic

45

30

30

20

Old suburb, low traffic

75

80

55

40

Old suburb, high traffic

120

160

90

55

 

To calculate an SQG(NOEC & EC10), the ABC value is added to the ACL(NOEC & EC10). ABC values vary with soil type. Therefore, it is not possible to present a single set of SQG(NOEC & EC10) values. Thus, two examples of SQG(NOEC & EC10) values for urban contaminated soils are provided below. These examples would be at the low and high end of the range of SQGs values (but not the extreme values) generated for Australian soils.

 

Example 1

Site descriptors urban residential/public open space land use in a new suburb.

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with a 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   45 mg/kg

ABC:     10 mg/kg

SQG(NOEC & EC10):   55 mg/kg

 

Example 2

Site descriptors – commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   480 mg/kg[1]

ABC:    40 mg/kg

SQG(NOEC & EC10):   520 mg/kg

As indicated in the exposure pathway assessment, the log Kd values for Zn measured in a range of Australian soils were below 3 and therefore there is the potential in some soils for Zn to leach to groundwater and effect aquatic ecosystems. Although the calculation of SQGs based on protecting aquatic ecosystems from the effects of leached contaminants is not included in the EIL derivation methodology (Schedule B5b), the calculations are presented here to illustrate the recommended approach and what effect this has on the resulting SQGs. The following SQGs were based on the ACL(NOEC & EC10) values for urban residential/public open space land use.

 

The soil-specific SQGs for Zn that accounted for leaching potential were calculated using the US EPA method (US EPA 1996).

 

SQG = Cw . (Kd + (θw + θa . H) / ρb) . DAF    (equation 2)

 

where SQG is the appropriate soil quality guideline in soil (mg/kg), Cw is the target soil leachate concentration (mg/L) (that is, the Australian and New Zealand freshwater quality guideline for Zn, (ANZECC and ARMCANZ 2000)), Kd is the soilwater partition coefficient (L/kg), θw is the water-filled soil porosity Lwater/Lsoil), θa is the air-filled soil porosity (Lair/Lsoil), ρb is the dry soil bulk density (kg/L), H is the Henry’s law constant (unitless), and DAF is the dilution and attenuation factor[2]. The values of DAF used in the calculations were 1 and 20. There is a linear relationship between the DAF and the SQGs, thus the SQGs calculated using a DAF of 20 are 20 times larger than those calculated using a DAF of 1.

 

The value for θw was set to 0.1 Lwater/Lsoil, θa was set to 0.1 Lair/Lsoil and ρb was set to 1.3 kg/L. The calculated SQG values when DAF was 1 and 20 are presented in Tables 15 and 16 respectively.

Table 15. Soil-specific zinc (Zn) soil quality guidelines (SQG(NOEC & EC10), mg total Zn/kg) based on protecting groundwater ecosystems from groundwater leaching when the dilution and attenuation factor (DAF) was 1.

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4

0.1

0.1

0.3

0.6

0.9

2

5

0.1

0.3

0.9

2

2

4

6

0.3

0.8

2

4

6

10

7

0.8

2

6

10

15

30

8

2

5

15

25

40

75

 


Table 16. Soil-specific zinc (Zn) soil quality guidelines (SQG(NOEC & EC10), mg total Zn/kg) based on protecting groundwater ecosystems from groundwater leaching when the dilution and attenuation factor (DAF) was 20.

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4

1

2

7

10

20

35

5

2

6

15

30

50

85

6

6

15

45

80

120

220

7

15

40

115

210

310

570

8

40

110

300

530

810

1500

 

In addition to calculating SQG(NOEC & EC10) values, two other sets of SQGs corresponding to two other levels of protection were generated. T hese were the SQG(LOEC & EC30), which indicate concentrations above which moderate toxic effects would occur and the SQG(EC50), which indicate concentrations above which marked toxic effects would occur.

The Zn SQG(LOEC and EC30) and SQG(EC50) and associated ACL values were calculated using the methodology, except the input data for the SSD was changed to the appropriate type (Table 1). This data is presented in Tables 24 and the raw data can be found in Appendix A. These measures of toxicity were not available in all instances, so, to maximise the data available to calculate SQG(LOEC and EC30) and SQG(EC50) values, the available toxicity data was converted to these measures using conversion factors. The NBRP (cited in Heemsbergen et al. 2008) derived a set of conversion factors for Cu and Zn (Table 17). These experimentally-based conversion factors were used rather than the generic conversion factors presented in Heemsbergen et al. (2008), which is consistent with the approach recommended in the  methodology for deriving SQGs. Table 18 shows the ACL(LOEC & EC30) and ACL(EC50) values for the Australian reference soil (that is, a pH of 6 and a CEC of 10 cmolc/kg) with areas of ecological significance, urban residential/public open space and commercial/industrial land uses. The set of soil-specific Zn ACL(LOEC & EC30) and ACL(EC50) values for each land use are presented in Tables 19 and 20.

 

Table 17. Conversion factors used to convert various measures of toxicity for cations such as copper and zinc. The conversion factors were obtained from unpublished data from the Australian National Biosolids Research Program and were cited by Heemsbergen et al. (2008).

Data being converted

Conversion factor

NOEC or EC10 to EC50

x 3

NOEC or EC10 to LOEC or EC30

x 1.5

LOEC or EC30 to EC50

x 2

 


Table 18. Zinc (Zn) added contaminant levels based on lowest observed effect concentration and 30% effect concentration data (ACL(LOEC & EC30)), and based on 50% effect concentration data (ACL(EC50)) for the Australian reference soil with various land uses.

Land use

ACL(LOEC& EC30) values

(mg/kg added Zn)

ACL(EC50) values

(mg/kg added Zn)

Areas of ecological significance

40

80

Urban residential/public open space

160

290

Commercial/industrial

250

450

 

Table 19. Soil-specific added contaminant limits based on lowest observed effect concentration and 30% effect concentration toxicity data (ACL(LOEC & EC30), mg/kg) for fresh zinc (Zn) that should theoretically provide the appropriate level of protection (that is, 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and CEC values ranging from 5 to 60 cmolc/kg. These are the recommended ACL(LOEC & EC30) values in freshly contaminated soils with each land use.

Areas of ecological significance

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

7

8

8

8

8

8

4.5

10

10

10

10

10

10

5.0

15

20

20

20

20

20

5.5

20

25

25

25

25

25

6.0

25

40

40

40

40

40

6.5

25

40

60

60

60

60

7.0

25

40

70

90

90

90

7.5

25

40

70

95

120

130

Urban residential/public open space land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

25

30

30

30

30

30

4.5

35

50

50

50

50

50

5.0

50

70

70

70

70

70

5.5

70

100

100

100

100

100

6.0

90

150

150

150

150

150

6.5

90

150

230

230

230

230

7.0

90

150

270

340

340

340

7.5

90

150

270

370

460

500

 


 

Commercial/industrial land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

45

50

50

50

50

50

4.5

60

75

75

75

75

75

5.0

80

110

110

110

110

110

5.5

110

170

170

170

170

170

6.0

140

250

250

250

250

250

6.5

140

250

360

360

360

360

7.0

140

250

420

540

540

540

7.5

140

250

420

590

730

800

Table 20. Soil-specific added contaminant limits based on 50% effect concentration toxicity data (ACL(EC50), mg/kg) for fresh zinc (Zn) that should theoretically provide the appropriate level of protection (that is, 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and cation exchange capacity (CEC) values ranging from 5 to 60 cmolc/kg. These are the recommended ACL(EC50) for Zn in freshly contaminated soils with each land use.

Areas of ecological significance

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

15

15

15

15

15

15

4.5

20

25

25

25

25

25

5.0

25

35

35

35

35

35

5.5

35

55

55

55

55

55

6.0

45

80

80

80

80

80

6.5

45

80

110

110

110

110

7.0

45

80

130

170

170

170

7.5

45

80

130

190

230

250

Urban residential/public open space land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

50

60

60

60

60

60

4.5

70

90

90

90

90

90

5.0

95

130

130

130

130

130

5.5

130

200

200

200

200

200

6.0

170

290

290

290

290

290

6.5

170

290

430

430

430

430

7.0

170

290

500

640

640

640

7.5

170

290

500

690

870

940

 


 

Commercial/industrial land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

80

95

95

95

95

95

4.5

100

150

150

150

150

150

5.0

150

200

200

200

200

200

5.5

200

300

300

300

300

300

6.0

250

450

450

450

450

450

6.5

259

450

650

650

650

650

7.0

259

450

750

1000

1000

1000

7.5

259

450

750

1100

1300

1400

 

The ABC values for freshly contaminated soils were calculated using the method set out in this Schedule and presented in Table 13.

In order to calculate the SQG(LOEC & EC30) and SQG(EC50) values the soil-specific ABC has to be added to the ACL(LOEC & EC30) and ACL(EC50) values, respectively. Therefore, the SQG(LOEC & EC30) and SQG(EC50) values will always be at least as large as those presented in Tables 19 and 20. Examples of the SQG(LOEC & EC30) and SQG(EC50) values are provided below.

 

SQG(LOEC & EC30)Example 1

Site descriptors urban residential/public open space land use in a new suburb.

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with a 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30)

70

mg/kg

ABC

10

mg/kg

SQG(LOEC & EC30)

80

mg/kg

 

SQG(LOEC & EC30)Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30)

730

mg/kg

ABC

  40

mg/kg

SQG(LOEC & EC30)

770

mg/kg

 


 

SQG(EC50)Example 3

Site descriptors urban residential/public open space land use in a new suburb.

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with a 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50)

130

mg/kg

ABC

  10

mg/kg

SQG(EC50)

140

mg/kg

 

 

SQG(EC50)Example 4

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50)

1300

mg/kg

ABC

    40

mg/kg

SQG(EC50)

1340

mg/kg

In addition to calculating SQGs in recently contaminated soils (that is, contamination is <2 years old), an equivalent set of levels was derived for soils where the contamination is aged (that is, it has been present for ≥2 years). The Zn SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) for aged sites were calculated using the methods set out in Schedule B5b and this Schedule, the only difference being that laboratory toxicity data based on freshly spiked soils or soils that had not been leached were multiplied by an ageing/leaching factor. A factor (3 for Zn) was developed by Smolders et al. (2009) that accounted for ageing and leaching of various metals. This ageing and leaching factor (ALF) has been incorporated into the methodology to derive the Flemish soil quality guidelines (VLAREBO 2008). Therefore, the raw toxicity data (Appendix A) for Zn that was generated using freshly spiked and non-leached soils was multiplied by this conversion factor and the geometric means for each species and soil process recalculated (Tables 21–23). It should be noted that the values in Tables 21–23 are not simply the data from Tables 24 multiplied by 3, as the correction factor was not applied to all the data (for example, data from the field-based NBRP was not adjusted).

The lowest geometric mean of the age-corrected toxicity data for each species/soil microbial process that was used to derive the aged ACL(NOEC & EC10) values is presented in Table 21 for soil processes, Table 22 for soil invertebrate species and Table 23 for plant species. The conversion of the fresh toxicity data to account for ageing/leaching and the resulting toxicity values are presented in Appendix A.

 

Table 21. The geometric mean values of the aged and age-corrected zinc (Zn) toxicity data (expressed in terms of added Zn) for soil processes.

Soil process

Geometric means (mg/kg added Zn)

 

EC10 or NOEC

EC30 or LOEC

EC50

Acetate decomposition

561

841

1681

Amidase

363

545

1091

Ammonification

295

443

885

Arylsulphatase

868

1303

2605

Glucose decomposition

274

1169

2904

Nitrate reductase

168

252

504

Nitrification

455

706

930

Phosphatase

2022

3033

6066

Respiration

313

470

940

Table 22. The geometric mean values of the aged and age-corrected zinc (Zn) toxicity data (expressed in terms of added Zn) for soil invertebrate species.

Invertebrate species

Geometric means (mg/kg added Zn)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Earthworm

A. caliginosa

669

823

1172

Earthworm

A. rosea

1172

1221

1308

Earthworm

E. fetida

602

888

1726

Earthworm

L. rubellus

659

855

1328

Earthworm

L. terrestris

3187

3771

5026

Nematode

Acrobeloides sp.

663

995

1989

Nematode

C. elegans

366

550

1099

Nematode

C. elegans (dauer larval stage)

2068

3103

6205

Nematode

Community nematodes

919

1378

2756

Nematode

Eucephalobus sp.

404

605

1210

Nematode

Plectus sp.

70

105

210

Nematode

Rhabditidae sp.

597

896

1791

Potworm

E. albidus

363

544

1088

Potworm

E. crypticus

828

1241

2483

Springtail

F. candida

566

848

1696

 


Table 23. The geometric mean values of the aged and age-corrected zinc (Zn) toxicity data (expressed in terms of added Zn) for plant species.

Species

Scientific name

Geometric means (mg/kg added Zn)

 

 

EC10 or NOEC

EC30 or LOEC

EC50

Alfalfa

M. sativa

595

892

1784

Barley

H. vulgare

110

306

652

Beet

B.vulgaris

595

892

1784

Black or white lentil

V. mungo

284

426

852

Canola

B. napus

230

328

409

Common vetch

V. sativa

127

190

380

Cotton

Gossypium sp.

272

288

293

Fenugreek

T. foenum graecum

318

477

953

Lettuce

L. sativa

793

1189

2379

Maize

Z. mays

460

694

1324

Millet

P. milaceum

540

1580

2026

Oats

A. sativa

667

1000

2000

Onion

A. cepa

198

297

594

Pea

P. sativum

793

1189

2379

Peanuts

A. hypogaea

140

224

280

Red clover

T. pratense

117

176

351

Sorghum

Sorghum sp.

256

528

924

Spinach

S. oleracea

396

595

1189

Sugar cane

Sacharum

3220

4830

9661

Tomato

L. esculentum

793

1189

2379

Triticale

Tritosecale sp.

998

1364

1658

Wheat

T. aestivum

640

928

1172

 

For each urban residential/public open space land use, soil-specific ACL(NOEC & EC10) values were derived separately for soil processes, soil invertebrate species and plant species (data not shown). Within each land use type, the soil-specific ACL(NOEC & EC10) values for each organism group were then merged so that the lowest ACL(NOEC & EC10) value for each combination of soil pH and CEC was adopted (Table 24). These should theoretically protect 99%, 80% and 60% of all soil processes, soil invertebrate species and plant species that are exposed to aged Zn contamination in soils that  are in an area of ecological significance, or have an urban residential/public open space, commercial/industrial land use, respectively.

Table 24. Soil-specific added contaminant limits based on no observed effect concentration and 10% effect concentration toxicity data (ACL(NOEC & EC10), mg/kg) for aged zinc (Zn) contamination that should theoretically provide the appropriate level of protection (i.e. 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and CEC values ranging from 5 to 60 cmolc/kg. These are the recommended ACL(NOEC & EC10) values for Zn in aged contaminated soils with each land use.


 

Areas of ecological significance

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

10

10

10

10

10

10

4.5

15

20

20

20

20

20

5.0

20

25

25

25

25

25

5.5

25

40

40

40

40

40

6.0

35

55

55

55

55

55

6.5

35

55

85

85

85

85

7.0

35

55

100

125

125

125

7.5

35

55

100

130

170

180

Urban residential/public open space land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

45

55

55

55

55

55

4.5

60

80

80

80

80

80

5.0

85

110

110

110

110

110

5.5

110

170

170

170

170

170

6.0

150

250

250

250

250

250

6.5

150

250

370

370

370

370

7.0

150

250

440

550

550

550

7.5

150

250

440

600

750

800

Commercial/industrial land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

70

85

85

85

85

85

4.5

100

120

120

120

120

120

5.0

125

180

180

180

180

180

5.5

180

270

270

270

270

270

6.0

230

400

400

400

400

400

6.5

230

400

590

590

590

590

7.0

230

400

690

870

870

870

7.5

230

400

690

940

1200

1300

 

The ABC values for aged Zn contamination used to calculate aged SQG(LOEC and EC30) and SQG(EC50) values were obtained from Olszowy et al. (1995) and are presented in Table 14.

SQGs are the sum of the ABC and ACL values, both of which are soil-specific. It is, therefore, not possible to present a single set of aged SQGs. Thus, some examples of aged SQGs for aged urban contaminated soils are provided below. The presented examples represent SQGs that would be at the low and high end of the range of SQGs that would be generated for Australian soils, but are not extreme values.


 

Example 1

Site descriptors – urban residential/public open space land use in an old NSW suburb with low traffic volume.

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with 1% iron and aged Zn contamination.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10)

110

mg/kg

ABC

75

mg/kg

SQG(NOEC & EC10)

185

mg/kg, which would be rounded off to 180 mg/kg.

 

Example 2

Site descriptors – commercial/industrial land use in an old Queensland suburb with a high traffic volume.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron and aged Zn contamination.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10)

1200

mg/kg

ABC

160

mg/kg

SQG(NOEC & EC10)

1360

mg/kg, which would be rounded off to 1400 mg/kg.

 

The Zn SQG(LOEC & EC30) and SQG(EC50) values for aged sites were calculated using the method described in this Schedule with the exception that aged or age-corrected Zn toxicity data was used (Tables 2123). Table 25 presents the ACL(LOEC & EC30) and ACL(EC50) values for the Australian reference soil (Table 6) for areas of ecological significance, urban residential/public open space, and commercial/industrial land uses.

 

The soil-specific ACL(LOEC and EC30) and ACL(EC50) values for aged Zn contamination and the various land uses are presented in Tables 26 and 27 respectively. As with the ACL(NOEC & EC10) values for aged Zn contamination, the ACL(LOEC & EC30) and ACL(EC50) values must have the soil-specific ABC added. Therefore, the SQG(LOEC & EC30) and SQG(EC50) values will be larger than the corresponding ACL values presented in Tables 26 and 27, respectively. Examples of the SQG(LOEC & EC30) and SQG(EC50) values are provided below.


Table 25. Zinc (Zn) ACLs for the Australian reference soil (pH = 6, CEC = 10 cmolc/kg) based on lowest observed effect concentration and 30% effect concentration toxicity data, and based on 50% effect concentration toxicity data.

Land use

ACL(LOEC & EC30) values (mg/kg added Zn)

ACL(EC50) values

(mg/kg added Zn)

Areas of ecological significance

90

140

Urban residential/public open space

400

700

Commercial/industrial

630

1100

 

Table 26. Soil-specific added contaminant limits based on lowest observed effect concentration and 30% effect concentration toxicity data (ACL(LOEC & EC30), mg/kg) for aged zinc (Zn) contamination that should theoretically provide the appropriate level of protection (i.e. 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and CEC values ranging from 5 to 60 cmolc/kg. These are the recommended ACL(LOEC & EC30) values for Zn in aged contaminated soils with each land use.

Areas of ecological significance

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

15

20

20

20

20

20

4.5

20

25

25

25

25

25

5.0

30

40

40

40

40

40

5.5

40

60

60

60

60

60

6.0

50

90

90

90

90

90

6.5

50

90

130

130

130

130

7.0

50

90

150

190

190

190

7.5

50

90

150

210

260

280

Urban residential/public open space land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

70

85

85

85

85

85

4.5

100

120

120

120

120

120

5.0

130

180

180

180

180

180

5.5

180

270

270

270

270

270

6.0

230

400

400

400

400

400

6.5

230

400

590

590

590

590

7.0

230

400

700

880

880

880

7.5

230

400

700

960

1200

1300


Commercial/industrial land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

110

130

130

130

130

130

4.5

150

190

190

190

190

190

5.0

210

290

290

290

290

290

5.5

280

420

420

420

420

420

6.0

360

620

620

620

620

620

6.5

360

620

920

920

920

920

7.0

360

620

1100

1400

1400

1400

7.5

360

620

1100

1500

1900

2000

 

Table 27. Soil-specific added contaminant limits based on 50% effect concentration toxicity data (ACL(EC50), mg/kg) for aged zinc (Zn) contamination that should theoretically provide the appropriate level of protection (i.e. 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.0 to 7.5 and cation exchange capacity (CEC) values ranging from 5 to 60 cmolc/kg. These are the recommended ACL(EC50) values for Zn in aged contaminated soils with each land use.

Areas of ecological significance

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

25

30

30

30

30

30

4.5

35

45

45

45

45

45

5.0

45

65

65

65

65

65

5.5

65

95

95

95

95

95

6.0

85

140

140

140

140

140

6.5

85

140

210

210

210

210

7.0

85

140

250

310

310

310

7.5

85

140

250

340

430

460

Urban residential/public open space land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

130

150

150

150

150

150

4.5

170

220

220

220

220

220

5.0

230

330

330

330

330

330

5.5

320

480

480

480

480

480

6.0

410

710

710

710

710

710

6.5

410

710

1100

1100

1100

1100

7.0

410

710

1200

1600

1600

1600

7.5

410

710

1200

1700

2100

2300

 


 

Commercial/industrial land use

pH

CEC (cmolc/kg)

5

10

20

30

40

60

4.0

200

230

230

230

230

230

4.5

270

350

350

350

350

350

5.0

370

510

510

510

510

510

5.5

510

760

760

760

760

760

6.0

650

1100

1100

1100

1100

1100

6.5

650

1100

1700

1700

1700

1700

7.0

650

1100

1900

2500

2500

2500

7.5

650

1100

1900

2700

3400

3600

The ABC values used for aged Zn contamination are presented in Table 14.

Both the ACL and ABC values for aged zinc contamination are soil-specific therefore a single set of SQGs could not be presented. Thus, examples from the low and high portions of the range of SQG(LOEC & EC30) and SQG(EC50) are presented below.

 

SQG(LOEC & EC30)Example 1

Site descriptors urban residential/public open space land use in an old NSW suburb with low traffic volume.

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30)

180

mg/kg

ABC

75

mg/kg

SQG(LOEC & EC30)

255

mg/kg

This SQG(LOEC & EC30) would then be rounded off using the rules in section 2.1 to a value of 250 mg/kg.

 

SQG(LOEC & EC30)Example 2

Site descriptors commercial/industrial land use in an old Victorian suburb with high traffic volume.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30)

1900

mg/kg

ABC

55

mg/kg

SQG(LOEC & EC30)

1955

mg/kg

This SQG(LOEC & EC30) would then be rounded off using the rules in section 2.1 to a value of 2000 mg/kg.

 

SQG(EC50)Example 3

Site descriptors urban residential/public open space land use in an old NSW suburb with low traffic volume.

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50)

330

mg/kg

ABC

75

mg/kg

SQG(EC50)

405

mg/kg

This SQG(EC50) would then be rounded off using the rules in section 2.1 to a value of 400 mg/kg.

 

 

SQG(EC50)Example 4

Site descriptors commercial/industrial land use in an old Victorian suburb with high traffic volume.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50)

3400

mg/kg

ABC

55

mg/kg

SQG(EC50)

3455

mg/kg

This SQG(EC50) would then be rounded off using the rules in section 2.1 to a value of 3500 mg/kg.

 

Based on the criteria established in the methodology for SQG derivation (Schedule B5b), the Zn SQGs were considered to be of high reliability. This occurred as the toxicity data set easily met the minimum data requirements to use the SSD method and normalisation relationships were available to account for soil characteristics.

A compilation of SQGs for Zn from a number of jurisdictions is presented in Table 28. These SQGs have a variety of purposes and levels of protection and therefore comparison of the SQGs between each other and with the Zn SQGs is problematic. The guidelines for Zn range from 20 mg/kg (added Zn) for the Netherlands to 200 mg/kg (total Zn) for Canada. The superseded interim urban EIL (NEPC 1999) was 200 mg/kg total Zn and therefore at the top of the range of the international Zn guidelines.

 

The Zn ACL(NOEC & EC10) values in freshly contaminated urban residential/public open space soils ranged from 20330 mg/kg (added Zn) (Table 10). The corresponding values for urban residential/public open space soils with aged Zn contamination ranged from 45810 mg/kg (Table 24). The lowest ACLs (for sandy acidic soils) were very similar to the lowest of the international SQGs, but considerably lower than the superseded interim urban EIL. However, the largest ACLs (for neutral to alkaline, high CEC soils) were considerably larger than any of the international SQGs apart from the Dutch intervention level, which has a different purpose from the ACLs. Thus, in soils where the Zn has a low bioavailability, higher concentrations of Zn are permitted under the methodology than under the superseded interim urban EIL.

 

The intervention value in the Netherlands is 720 mg/kg total Zn. The range of ACL(EC50) values (which most closely relate to the Dutch intervention value) in freshly contaminated urban residential/public open space soils was 50940 mg/kg (Table 20). While the range for aged Zn contamination was 1252,300 mg/kg (Table 27), the Dutch value corresponds to the 60th and 25th percentile of the range of ACL(EC50) values for fresh and aged Zn contamination respectively. Therefore, depending on soil physicochemical properties, the ACL(EC50) values would permit considerably less (in high bioavailability soils) to considerably more (in low bioavailability soils) Zn than in the Netherlands.

 

Table 28. Soil quality guidelines for zinc (Zn) from international jurisdictions.

Name of zinc limit

Numerical value of the limit (mg/kg)

Dutch intervention level1

720 (added Zn)

Dutch maximum permissible addition1

20 (added Zn)

Canadian SQG (residential)2

200 (total Zn)

Eco-SSL plants3

160 (total Zn)

Eco-SSL soil invertebrates3

120 (total Zn)

Eco-SSL avian3

46 (total Zn)

Eco-SSL mammalian3

79 (total Zn)

EU soil guidelines using negligible risk4

67150 (total Zn)

1 = VROM, 2000

2 = CCME, 1999a and 2006 and http://www.ccme.ca/publications/list_publications.html#link2

3 =  http://www.epa.gov/ecotox/ecossl/ 

4 = Carlon, 2007

4                   Arsenic

The metalloid As occurs in a number of oxidation states: -3 (-III), 0, +3 (III) and +5 (V). Arsenic (III) is the dominant form under reducing conditions and As (V) is the dominant form in oxidised soils. The SQG derivation methodology (Schedule B5b) is only suitable for the aerobic portion of soils. SQGs for As were therefore calculated using only well oxidised soil studies. Therefore, arsenic will predominantly be present as As (V) but, as all the toxicity studies expressed toxicity in terms of total arsenic, the SQGs generated in this study are for total arsenic. For waterlogged soils, a separate As SQG should be derived, due to the difference between As (III) and As (V) in both toxicity and bioavailability in these soils. The chemical abstract service number (a unique identification number for each chemical) for As is 7440-38-2.

The two key considerations in determining the most important exposure pathways for inorganic contaminants such as As are whether they biomagnify and whether they have the potential to leach to groundwater. A surrogate measure of the potential for a contaminant to leach is its watersoil partition coefficient (Kd). If the logarithm of the Kd (log Kd) of an inorganic contaminant is less than 3 then it is considered to have the potential to leach to groundwater (Schedule B5b). The log Kd reported by Crommentuijn et al. (2000) was 2.28 L/kg, so As has the potential in some soils to leach to groundwater. This is consistent with information regarding human health problems experienced in Bangladesh from the presence of As in groundwater. The methodology for EIL derivation (Schedule B5b) does not advocate the routine derivation of EILs that account for leaching potential. Rather, it advocates that this is done on a site-specific basis as appropriate. However, the calculations are presented here to illustrate the recommended approach and the effect that this would have on the resulting SQGs.

 

Arsenic is not known to biomagnify in oxidised soils (Heemsbergen et al. 2009) and therefore only direct toxicity routes of exposure were considered in deriving the SQGs.

The raw toxicity data for As is presented in Appendix B. The toxicity data (geometric means for each species) used to calculate the SQGs is presented in Table 29. There was toxicity data for three soil invertebrate species, five terrestrial animal species and 13 species of plants. These meet the minimum data requirements recommended by Heemsbergen et al. (2008) to use the BurrliOZ SSD method (Campbell et al. 2000).

Table 29. Geometric mean values of arsenic (As) toxicity data (expressed in terms of total As) for soil invertebrate species, terrestrial bird and mammal species and plant species.

Test species

Geometric mean (mg/kg)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Bean

Phaseolus vulgaris

22.6

84

168

Blueberry

Vaccinium sp.

22.2

55

111

Common rat

Rattus norvegicus

10.0

25

50

Corn

Z. mays

25.1

67

123

Cotton

Gossypium sp.

20.8

52

104

Deer mouse

Peromyscus maniculatus

320

1600

1600

Earthworm

Eisenia fetida

20.0

100

100

Earthworm

L. rubellus

76.1

381

381

Earthworm

L. terrestris

100

250

500

Fulvous whistling duck

Dendrocygna bicolour

229

1145

1145

Grass

 

13.4

81

161

Northern bobwhite

Colinus virginianus

54.0

270

270

Oat

A. sativa

22.7

44

70

Pea

Pisum sativum

20.8

52

104

Pine

 

292

731

1462

Potato

Solanum tuberosum

36.3

108

181

Radish

Raphanus sativa

67.7

169

339

Sheep

Ovis aries

25.0

63

125

Soyabean

Glycine max

9.7

24

35

Tomato

L. esculentum

62.5

166

263

Wheat

T. aestivum

43.4

153

307

 

In order to maximise the use of the available toxicity data, conversion factors (adopted from the Australian and New Zealand guidelines for fresh and marine water quality (ANZECC & ARMCANZ 2000) by Heemsbergen et al. (2008)) were used to permit the inter-conversion of NOEC, LOEC, EC50, EC30 and EC10 data. Conversion factors for cations (for example, Cu and Zn) were developed by the NBRP and recommended by Heemsbergen et al. (2008) in preference to the default conversion factors adopted from the WQGs. However, as As is predominantly found in anionic form in soils, the default conversion factors were used (Table 30).

 

Table 30. The default conversion factors used to convert different measures of toxicity to chronic no observed effect concentrations (NOECs) or 10% effect concentrations (EC10). Sourced from Heemsbergen et al. (2008), who adopted the values from the Australian and New Zealand guidelines for fresh and marine water quality (ANZECC & ARMCANZ 2000).

Toxicity dataa

Conversion factor

EC50 to NOEC or EC10

5

LOEC or EC30 to NOEC or EC10

2.5

MATC* to NOEC or EC10

2

 a EC50 is the concentration that causes a 50% effect, EC30 is the concentration that causes a 30% effect, EC10 is the concentration that causes a 10% effect, NOEC = no observed effect concentration, LOEC = lowest observed effect concentration, *MATC = the maximum acceptable toxicant concentration and is the geometric mean of the NOEC and LOEC.

It is well known that soil physicochemical properties affect the toxicity and bioavailabiity of As. However, this knowledge is qualitative. For example, Sheppard (1992) reviewed the existing literature and concluded that the toxicity of As was five times more toxic in sands and loams than in clay soils. There is only one set of published normalisation relationships for As toxicity (Song et al. 2006). This relates the toxicity of As (i.e. barley root elongation) expressed in terms of total added As, ammonium sulphate [(NH4)2SO4]-extractable As or ammonium phosphate (NH4H2PO4)-extractable As to soil properties such as oxalate-extractable Mn and oxalate-extractable Fe concentrations. The normalisation relationships for EC10 and EC50 toxicity data expressed in terms of total added As (from Song et al. 2006) are:

EC10 = 0.1 (oxalate-extractable Mn) + 1.03 (% clay) – 9.25   (equation 3)

(r2 adj = 0.89, p = <0.001, n = 16)

 

EC50 = 0.21 (oxalate-extractable Mn) + 0.016 (oxalate-extractable Fe) 

+ 4.29 (% clay) – 48.2      (equation 4)

(r2 adj = 0.91, p = <0.001, n = 16)

 

However, with the exception of the Song et al. (2006) data, none of the available As toxicity studies had expressed the toxicity in the units of the normalisation relationships nor had the studies measured the soil properties used in the normalisation relationships. Therefore, the normalisation relationships could not be used.

Figure 4 shows the SSD (that is, the cumulative distribution of the geometric means of species sensitivities to As) for all species for which As toxicity data was available. The distribution of the major groups of organisms along the SSD is uniformthus all of the organism groups have a smilar sensitivity to As.

 

Figure 4. The species sensitivity distribution (plotted as a cumulative frequency against total arsenic (As) concentration) of As for soil invertebrate species, terrestrial vertebrate species and plant species.

The As toxicity data could not be normalised to the Australian reference soil because none of the publications had reported the properties required by the one normalisation relationship available for As. Thus, soil-specific ACLs could not be derived. Rather, a single generic ACL for each land use was derived. These generic ACLs would apply to all Australian soils of the appropriate land use. For example, the single ACL for urban residential /public open space land use would apply to all Australian urban residential/public open space soils.

All the available As toxicity data (apart from that of Song et al. 2006) were reported as total concentrations without making a distinction between added and background concentrations. The Hamon et al. (2004) method can predict the ABC for As in Australian soils. For European soils or toxicity studies, the Dutch background standardisation equation for As can be used (Lexmond et al. 1986):

As= 0.4*(clay content + organic matter content)   (equation 5)

 

However, the As toxicity studies did not report the Fe and Mn contents (required by the Hamon et al., 2004 method) or the organic matter or clay content (required by the Lexmond et al. 1986 method) of the soils in which the toxicity was determined. Therefore, it was not possible to estimate the ABC nor express toxicity in terms of added concentrations. As a result, no ACL values could be calculated.

 

The situation for As was that:

Therefore, only a single numerical value was generated by the BurrliOZ SSD method for each of the three land uses (that is, areas of ecological significance, urban residential/public open space, and commercial/industrial).

 

The output was the SQG(NOEC & EC10) for that particular land use and no soil-specific SQG(NOEC & EC10) values could be calculated. The As SQG(NOEC & EC10) values for the three land uses are presented in Table 31.

Table 31. Generic soil quality guidelines based on no observed effect concentration and 10% effect concentration toxicity data (SQG(NOEC & EC10)) for fresh arsenic (As) contamination in soil with different land uses.

Land use

SQG(NOEC & EC10)

(mg/kg total As)

Areas of ecological significance

8

Urban residential/public open space

20

Commercial/industrial

30

 

It should be noted, because As has generic SQG(NOEC & EC10) values, that they should be applied to all Australian soils that have the particular land use.

 

Despite the fact that ACLs could not be derived for As, the issue of background concentrations of As in Australian soils will be discussed as the situation could change in the future if additional data becomes available. If, in the future, toxicity data can be expressed in terms of added concentrations, it is recommended that the method of Hamon et al. (2004) be used to derive ABC values. Examples of the ABC values generated by the Hamon et al. (2004) method are presented in Table 32. The soil-specific estimate of ABC could be added to a generic ACL (if toxicity data could be expressed as added As, but no normalisation relationships were suitable) or it could be added to a soil-specific ACL (if it were possible to express the toxicity data in terms of added As and if normalisation relationships could be applied to the data).

Table 32. Ambient background concentrations of arsenic (As) estimated using the method of Hamon et al. (2004) as a function of the iron content of the soil.

Soil iron (%)

As (mg/kg)

0.1

1

1

3

10

12

20

18

 

The log Kd value for As (Crommentuijn et al. 2000) was below 3 and therefore in accordance with the  SQG derivation methodology (Schedule B5b) SQG(NOEC & EC10) values were derived to protect aquatic ecosystems from the effects of leached As from freshly contaminated soils.

 

The As SQG(NOEC & EC10) values based on protecting groundwater ecosystems were calculated using the US EPA method (US EPA 1996). The generic SQG(NOEC & EC10) values were calculated using DAF values of one and 20 and these are presented in Table 33. There is a linear relationship between the DAF and the SQGs, thus the SQGs calculated using a DAF of 20 are 20 times larger than those calculated using a DAF of 1.

Table 33. Generic arsenic (As) soil quality guidelines (SQGs, mg total As/kg) based on no observed effect concentration and 10% effect concentration toxicity data to protect groundwater ecosystems from leaching.

 

Dilution factor

1

20

SQG (mg/kg)

4.6

91

 

The SQG(LOEC & EC30) and SQG(EC50) values were calculated using the same method as for the As SQG(NOEC & EC10) values ,except that different toxicity data was used. The data used is presented in Table 29. To maximise the data available to generate the SQG(LOEC & EC30) and SQG(EC50) values, the available toxicity data was converted to the appropriate measure of toxicity using the default conversion factors presented in Table 30.

 

As with the SQG(NOEC & EC10) values for As, soil-specific SQG(LOEC & EC30) and SQG(EC50) values could not be generated, but rather a single generic SQG(LOEC & EC30) and SQG(EC50) value was generated for each of the three land uses (Table 34). Also, all toxicity data was expressed as total As rather than added As. As these are generic SQG(LOEC & EC30) and SQG(EC50) values ,they should be applied to all Australian soils with a particular land use.

 

Table 34: Generic soil quality guidelines based on lowest observed effect concentration and 30% effect concentration toxicity data (SQG(LOEC & EC30)), and based on 50% effect concentration toxicity data (SQG(EC50)) for soil with different land uses.

Land use

SQG(LOEC & EC30)

(mg/kg total As)

SQG(EC50)

(mg/kg total As)

Areas of ecological significance

20

30

Urban residential/public open space

50

90

Commercial/industrial

80

140

 

Song et al. (2006) conducted some experiments to determine the effect of ageing As over three months in four soils. They found that in all soils the toxicity and extractability decreased and the extent of the decrease ranged from 2- to 12-fold (Song et al. 2006). Yang et al. (2002) and Fendorf et al. (2004) also found that As aged in soils with the majority occurring within the first few months. Yang et al. (2002) also found that As ageing did not always occurit occurred in only 47% (i.e. 17 out of 36) of the soils they examined. Song et al. (2006) found that the extent of ageing was significantly correlated with oxalate-extractable iron and Olsen-P concentrations in the four test soils. However, they also noted that data on more soils was needed in order for the relationships to be considered more robust. Song et al. (2006) concluded that ageing of As ‘should be taken into account during risk assessment’. Therefore, in order to account for ageing in a conservative manner (that is, one that is protective of the environment), the lowest ALF factor (2) determined by Song et al. (2006) was used to derive the aged SQGs. This ALF was applied to all the toxicity data.

As the available toxicity data can only be expressed as total As concentrations, ACL values could not be derived, so SQGs were derived. The ALF of 2 was applied to all the toxicity data; therefore the aged SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values are exactly twice the corresponding fresh SQGs for arsenic. The resulting aged SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values are presented in Table 35.

Table 35. Generic soil quality guidelines based on no observed effect concentration and 10% effect concentration toxicity data (SQG(NOEC & EC10)), lowest observed effect concentration and 30% effect concentration toxicity data (SQG(LOEC & EC30)), and based on 50% effect concentration toxicity data (SQG(EC50)) for soil with different land uses.

Land use

SQG(NOEC & EC10)

(mg/kg total As)

SQG(LOEC & EC30)

(mg/kg total As)

SQG(EC50)

 (mg/kg total As)

Areas of ecological significance

15

40

60

Urban residential/public open space

40

100

180

Commercial/industrial

60

160

290

Background levels of As are not elevated by historic pollution in urban residential/public open space soils, as can be seen by data from Olszowy et al. (1995) (Table 36). Therefore, in the future, if toxicity data can be expressed in terms of added concentrations, it is recommended that the method of Hamon et al. (2004) be used to estimate background values, as they are soil-specific. Examples of the ABC values generated by the Hamon et al. (2004) method are presented in Table 32.

 

Table 36. Background concentrations of arsenic (As) from Olszowy et al. (1995) in suburbs of different age and with different intensities of traffic in various states of Australia.

Suburb type

25th percentile As (mg/kg)

 

NSW

QLD

SA

VIC

New suburb, low traffic

5

3

5

NA

New suburb, high traffic

5

3

5

NA

Old suburb, low traffic

5

4

5

5

Old suburb, high traffic

5

3

5

5

NA = not available

The As toxicity dataset met the minimum data requirements to use the SSD method but there were no normalisation relationships available to account for soil characteristics. Based on the criteria for assessing the reliability of SQGs (Schedule B5b), this means that the As SQGs were considered to be of moderate reliability.

A compilation of SQGs for As from a number of jurisdictions is presented in Table 37. These guidelines have a variety of purposes and levels of protection and therefore comparison of the values is problematic. The SQGs for As range from 4.5 mg/kg (added As) for the Dutch to 110 mg/kg (total As) for another European country. The superseded interim urban EIL (NEPC 1999) was 20 mg/kg total As and lies in the lower portion of the range of As SQGs. The As SQG(NOEC & EC10) for freshly contaminated urban residential/public open space soils was 20 mg/kg (total As) and thus identical to the superseded interim urban EIL. The SQG(NOEC & EC10) for aged contamination at 40 mg/kg is twice the superseded interim urban EIL for As.

 

The SQG(LOEC & EC30) and SQG(EC50) values for As in freshly contaminated urban residential/public open space soils are 50 and 80 mg/kg respectively. The SQG(LOEC & EC30) is in the middle of the range of SQGs for other jurisdictions, while the SQG(EC50) is in the upper portion of the range of SQGs. The aged As SQG(LOEC & EC30) for urban residential/public open space soils lies in the upper part of the range of international SQGs while the aged As SQG(EC50) value for urban residential/public open space soils is markedly larger than any other international SQG.

 

Table 37. Soil quality guidelines for arsenic (As) from international jurisdictions.

Name of arsenic soil quality guideline

Numerical value of the guidelines (mg/kg)

Dutch target value1

29    (total As)

Dutch maximum permissible addition1

4.5 (added As)

Canadian SQG2

12    (total As)

Eco-SSL plants3

18    (total As)

Eco-SSL soil invertebrates3

NA

Eco-SSL avian3

43    (total As)

Eco-SSL mammalian3

46    (total As)

EU screening values potential risk in residential areas4

5110 (total As)

1 = VROM 2000

2 = CCME, 1999b, and 2006 and http://www.ccme.ca/publications/list_publications.html#link2

3 =  http://www.epa.gov/ecotox/ecossl/

4 = Carlon 2007

NA = not available

 

5                   Naphthalene

Unlike Zn and As, which can occur in several forms in soil, naphthalene is a unique compound and only information relating to it was used in the derivation of the SQG values. Naphthalene (C10H8) is the smallest of the family of compounds collectively termed polycyclic aromatic hydrocarbons (PAHs). The chemical abstract service number for naphthalene is 91-20-3 (HSDB 2004).

Selected physicochemical properties of naphthalene are:

 

Molecular weight:   128.17 (O’Neil 2001)

Log Kow    3.29 (US EPA 1982),

 3.013.45 (Verschueren 1983),

 3.30 (Hansch et al. 1995)

Log Koc    2.97 (US EPA 1982; GDCH 1992; Kenaga 1980)

Vapour pressure   0.087 mm Hg (US EPA 1982)

 0.085 mm Hg at 25°C (Ambrose et al. 1975)

Aqueous solubility  31 mg/L at 25°C (Pearlman et al. 1984)

Henry’s law constant 4.6 x 10-4 atm-m3/mol (US EPA 1982; Yaws et al. 1991)

 4.4 x 10-4 atm-m3/mol (Shiu & Mackay 1997)

Half-life (in soil)  218 days (ATSDR 2005)

The minimum log Kow value at which biomagnification should be considered in the derivation of SQGs is 4 (Schedule B5b). As the reported log Kow values for naphthalene were below 4 and it has a relatively short half-life (see above), it is not considered a biomagnifying compound and the normal protection levels were used. Therefore only the direct toxicity exposure route was considered in the derivation of SQGs for naphthalene. The log Koc value for naphthalene is moderate (~3) and therefore there is only a moderate potential for naphthalene to be leached to groundwater or surface water. Soil quality guidelines to protect aquatic ecosystems were therefore not generated.

Toxicity data for naphthalene was available for two plant species, eight species of soil invertebrates and four species of terrestrial vertebrates (Table 38). In total, there was data for 14 species that belonged to five taxonomic groups and thus this met the minimum data requirements recommended by the methodology to use the BurrliOZ SSD method (Campbell et al. 2000). Table 38 shows the geometric means of individual species used to derive the naphthalene SQGs. The raw toxicity data used to generate the species geometric means are presented in Appendix E.

 

In order to maximise the use of the available toxicity data, default conversion factors were used to permit the inter-conversion of NOEC, LOEC, EC50, EC30 and EC10 data (Table 30).

 


Table 38. Geometric means of the toxicity of naphthalene (expressed in terms of total naphthalene) to soil invertebrates, terrestrial vertebrates and plants.

Test species

Geometric mean (mg/kg)

Common name

Scientific name

NOEC or EC10

LOEC or EC30

EC50

Earthworm

Eisenia fetida

54

135

270

European rabbit

Oryctolagus cuniculus

2000

5000

10 000

House mouse

Mus musculus

407

1018

2036

Lettuce

L. sativa

21

54

107

Mite

Acari spp

232

580

1160

Mite

Mesostigmata spp.

195

487

973

Mite

Oribatida sp.

219

547

1094

Northern bobwhite

C. virginianus

1000

2500

5000

Common rat

R. norvegicus

1000

2500

5000

Radish

R. sativa

61

153

305

Spider

Grammonata inornata

177

443

886

Springtail

Collembola spp.

214

535

1070

Springtail

F. fimetaria

20

50

100

Springtail

Poduromorpha spp.

203

508

1016

 

It is well known that the organic carbon (OC) or organic matter content of soils affects the toxicity and bioavailabiity of organic contaminants such as naphthalene. European guidelines use normalisation relationships for organic contaminants (ECB 2003), but these have not yet been verified for Australian soils. In fact, when data for soils with OC contents greater than typical Australian soils was removed, OC was no longer a useful descriptor of toxicity (Broos et al. 2007). While the above example is for an inorganic contaminant, it shows the potential for European normalisation relationships to be inappropriate for Australia. As Australian soils are in general low in organic carbon, it was not recommended to use European normalisation relationships (Schedule B5b). There were no normalisation relationships available for naphthalene. Therefore, the toxicity data could not be normalised to the Australian reference soil, nor could soil-specific SQGs be derived.

The SSD for the naphthalene toxicity data is presented in Figure 5. As there was only toxicity data for 14 different species, insufficient data was available to make a robust assessment of the relative sensitivity of the groups of organisms. Nonetheless, it appears that plant and soil invertebrate species were more sensitive to naphthalene than vertebrate species, as the vertebrate toxicity data was all higher than those for other species. An argument could be mounted to exclude the terrestrial vertebrates from the calculation of the SQGs; however, this was not adopted, for three reasons. Firstly, the data was sparse and therefore the differences in the relative sensitivity of the groups of organisms may not be real. Secondly, the terrestrial vertebrates represent a major group of organisms that most people would wish to be able to maintain in urban residential/public open space settings. Thirdly, removal of these species only had a minor effect on the resulting SQG(NOEC & EC10) (i.e. the PC80 for all species was 68 mg/kg while the corresponding value when the vertebrates were removed was 60 mg/kg).

Figure 5. The species sensitivity distribution (plotted as a cumulative frequency of the toxicity data against naphthalene soil concentration) of soil invertebrates, plants and terrestrial vertebrates to naphthalene.

Given that (a) there was sufficient toxicity data to use the BurrliOZ software, (b) the data could not be normalised to the Australian reference soil, and (c) the toxicity data could not be expressed in terms of added concentrations, it meant that there was a single output from the BurrliOZ SSD for each of the three land uses (that is, areas of ecological significance, urban residential/public open space, and commercial/industrial). Therefore, the output from the SSD was a single generic (not soil-specific) SQG for each land use.

The generic SQGs for naphthalene in soils with each of the three land uses are presented in Table 39.

 

Table 39. Generic soil quality guidelines for naphthalene in freshly contaminated soils with different land uses based on no observed effect concentration and 10% effect concentration toxicity data.

Land use

SQG(NOEC & EC10)

(mg/kg total naphthalene)

Areas of ecological significance

5

Urban residential/public open space

70

Commercial/industrial

150

 

There is no equation available to estimate the background concentration of naphthalene. Naphthalene is produced by some organisms (for example, magnolias and termites) but at very low concentrations, which are negligible in terms of ABC values. Naphthalene can also be synthesised as a result of fires and in fire-prone areas and it might be appropriate to determine naphthalene ABC values.

 

In most soils, naturally occurring naphthalene concentrations will be negligible. For the purpose of this guideline the ABC for naphthalene was assumed to be 0 mg/kg. Therefore, the reported toxicity values which were expressed as total naphthalene were identical to the data when expressed as added naphthalene concentrations (that is, total concentration – 0 = added concentration) and therefore the ACLs derived using the SSD methodology equalled the SQGs.

 

It should be noted that if a soil-specific ABC for naphthalene is determined then that could be added to the above values to obtain a soil-specific SQG. Otherwise, these generic SQGs are applicable to all Australian soils with these particular land uses.

These SQGs were calculated using the same method as that for the SQG(NOEC & EC10) values for naphthalene, except that different toxicity data was used (Table 38). To maximise the data available to generate SQG(LOEC & EC30) and SQG(EC50) values, the available toxicity data was converted to the appropriate measure of toxicity using the default conversion factors recommended in Schedule B5b and presented in Table 30.

 

As with the SQG(NOEC & EC10) values for naphthalene, soil-specific ACL(LOEC & EC30) and ACL(EC50) values could not be generated, so rather a single generic SQG(LOEC & EC30) and SQG(EC50) was generated for each of the three land uses (Table 40). It should be noted that if a soil-specific ABC for naphthalene is determined then that could be added to the generic SQG values (Table 40) to obtain a soil-specific SQG. Otherwise these generic SQG(LOEC & EC30) and SQG(EC50) values should apply to all Australian soils with these particular land uses.

 

Table 40. Generic soil quality guidelines for naphthalene in freshly contaminated soil with different land uses based on lowest observed effect concentration and 30% effect concentration toxicity data and based on 50% effect concentration toxicity data.

Land use

SQG(LOEC & EC30)

(mg/kg total naphthalene)

SQG(EC50)

(mg/kg total naphthalene)

Areas of ecological significance

10

25

Urban residential/public open space

170

340

Commercial/industrial

370

730

 

There is currently no ageing or leaching factor available for naphthalene in the literature and therefore SQGs for aged contamination could not be derived.

The most well known metabolites of naphthalene are 1-naphthol (CAS no. 90-15-3) or 2-naphthol (CAS no. 135-19-3). These compounds are both known to affect plant growth and are suspected to have endocrine disrupting properties (Pesticide Action Network at <www.pesticideinfo.org>). There is no toxicity data in soils or SQGs reported for these compounds.

The naphthalene toxicity dataset met the minimum data requirements to use the SSD method but there were no normalisation relationships available to account for soil characteristics. Based on the criteria for assessing the reliability of SQGs (Schedule B5b), the naphthalene SQGs were considered to be of moderate reliability.

A compilation of SQGs for naphthalene in a number of jurisdictions is presented in Table 41. These SQGs have a variety of purposes and levels of protection and therefore comparison of the values is problematic. The SQGs for naphthalene range from 0.6 mg/kg for Canada to 125 mg/kg for the USA, both expressed as total naphthalene. The original NEPM (NEPC 1999) did not include an EIL for naphthalene. The SQG(NOEC & EC10) for areas of ecological significance freshly contaminated with naphthalene is 5 mg/kg and thus is identical to the lower range of values set within the EU, but approximately an order of magnitude higher than the Canadian SQG and 1/25th of the USA SQG. The  SQG(NOEC & EC10) for urban residential/public open space is 70 mg/kg and thus slightly higher than the highest EU SQGs but still approximately half the US EPA screening level for residential land. The SQG(LOEC & EC30) for urban residential land use at 170 is 40% larger than the US EPA screening level, while the corresponding SQG(EC50) value is 2.8 times the US EPA screening level.

 

Table 41. Soil quality guidelines for naphthalene in a number of jurisdictions.

Name of the naphthalene soil quality guideline

Value of the guidelines (mg/kg)

Canadian SQG (residential)1

0.6

EU (residential)2

560

US EPA Screening level (residential)3

125

1 = CCME 1999c , 2006 and <http://www.ccme.ca/publications/list_publications.html#link2>

2 = Carlon 2007

3 = http://www.epa.gov/ecotox/ecossl/.

 

6                   DDT

DDT is the abbreviation used for dichloro-diphenyl-trichloroethane (C14H9Cl5). Technical grade DDT (the form used in pesticide formulations) consists of 14 compounds (ATSDR 2002). The active ingredient and the main constituent of DDT is p,p’-DDT (approx 87% of DDT). Other compounds present include o,p’-DDT (15% of DDT), dichloro-diphenyl-dichloroethylene (DDE) and dichloro-diphenyl-dichloroethane (DDD), which are also metabolites and breakdown products of DDT. When DDT is referred to, usually people are referring to p,p’-DDT and this was the form that was used for the derivation of the EIL. The CAS registration number for p,p’-DDT is 50-29-3.

Selected physicochemical properties of DDT include:

Molecular weight  354.49 (Howard & Meylan 1997)

Log Kow   6.91 (Howard & Meylan 1997; Hansch et al. 1995)

Log Koc   5.18 (Swann et al. 1981)

Vapour pressure   1.60 x 10-7 at 20°C (Bidleman & Foreman 1987)

Aqueous solubility   0.025 mg/L at 25°C (Howard & Meylan 1997),

 5.5 x 10-3 mg/L at 25°C (Yalkowsky & Dannenfelser 1992)

Henry's law constant  8.3 x 10-6 atm-m3/mol (Howard & Meylan 1997)

Half-life (in aerobic soil)  range from 2 years (Lichenstein & Schulz 1959) to greater than 15 years (Keller 1970; Stewart & Chisholm 1971)

Half-life (in anaerobic soil) 16100 days (Castro & Yoshida 1971)

Half-life of DDT  190 years (OMEE 1993)

Bioconcentration factor 2.516 (CCME 1999d)

Bioaccumulation factor 0.929 (CCME 1999d)

DDT is a well known biomagnifying contaminant and, as the log Kow is higher than 4, both the direct toxicity and biomagnification routes of exposure needed to be accounted for in deriving the SQGs. Therefore, the level of protection (that is, percentage of species to be protected) was increased for urban residential/public open space soils from 80% to 85% as recommended in Schedule B5b. The log Koc value for DDT is >5 and therefore there is a very low potential for DDT to be leached to groundwater or surface water.

The raw toxicity data available for DDT is presented in Appendix F. The geometric means of toxicity data for each species and soil process are presented in Table 42. There was toxicity data for a total of 15 species or soil processes that belong to 5 different taxonomic groups or nutrient groups. Thus, there was sufficient toxicity data to use the SSD method to derive SQGs for DDT.

As with naphthalene, it is well known that the organic carbon or organic matter content of soils affects the toxicity and bioavailabiity of organic contaminants such as DDT. However, there were no normalisation relationships available for DDT. Therefore, the toxicity data could not be normalised to the Australian reference soil (Table 6), nor could soil-specific SQGs be derived.

Figure 6 shows the SSD (that is, the cumulative distribution of the geometric means of toxicity values) for the species used to derive the DDT SQGs. There is a general paucity of terrestrial toxicity data for DDT. This is particularly the case for plants and soil invertebrates where each group only has data for two species. It is therefore difficult to assess the relative sensitivity of these groups of organisms. Soil processes had sensitivities to DDT ranging from very sensitive to very tolerant, although most were in the more tolerant part of the distribution. Both plants were tolerant of DDT. Both soil invertebrates had moderate sensitivity while the vertebrate species were generally sensitive. The greater sensitivity of the vertebrates is consistent with the findings on the relative sensitivity of aquatic species.

Table 42. The geometric mean values of the DDT toxicity data for soil invertebrate species, terrestrial vertebrate species, plant species and soil processes.

Test species

Geometric means (mg/kg)

Common name

Scientific name

NOEC or EC10

LOEC or EC30

EC50

Earthworm

Eisenia fetida

363

1131

2499

Field mustard

Brassica rapa

1000

2500

5000

Helmeted guineafowl

Numida meleagris

30

75

150

House sparrow

Passer domesticus

600

1500

3000

Japanese quail

Coturnix japonica

80

200

400

Mallard duck

Anas platyrhynchos

24

59

119

Northern bobwhite

C. virginianus

68

170

341

Oats

A. sativa

1000

2500

5000

Ring-necked pheasant

Phasianus colchicus

104

261

522

Soil process

Ammonification

1250

3125

6250

Soil process

Nitrification

56

141

281

Soil process

Respiration

1000

2500

5000

Soil process

SIN

1000

2500

5000

Soil process

SIR

1000

2500

5000

Springtail

F. candida

464

1344

2836

Figure 6. The species sensitivity distribution (plotted as a cumulative frequency of the toxicity data against DDT soil concentration) of soil invertebrate species, soil processes, plant species and terrestrial vertebrate species to DDT.

All the available DDT toxicity data was reported as total concentrations without making a distinction between added and background concentrations. There was no equation available able to estimate the background concentration of DDT. DDT only occurs due to its synthesis by humans. There is therefore no natural background concentration of DDT. However, due to its persistence and its ability to volatilise, DDT can be subject to long-distance transport. In fact, a global distillation hypothesis was developed and has widely been accepted as the explanation of the presence of DDT and its metabolites and other persistent organic pollutants in polar ecosystems, which have no nearby industrial point sources or non-point sources. Because of this global transport of DDT, it could be argued that there is an ABC. As the DDT toxicity studies did not provide any estimate of the ABC for DDT either at the sites or in the soils that were used, this could not be accounted for in deriving the limits for DDT. Therefore, a default ABC for DDT of 0 mg/kg was adopted.

The situation for DDT was that:

Therefore, a single value was generated by BurrliOZ (Campbell et al. 2000) for each of the three land uses. The output was the SQG(NOEC & EC10) for each particular land use and no soil-specific SQGs could be calculated. As DDT biomagnifies, the SQGs must take this into account. The methodology for deriving SQGs (Schedule B5b) for biomagnifying contaminants is to increase the level of protection (% of species to be protected) by 5% for soils for urban residential/public open space and commercial/industrial land uses to 85% and 65% of species respectively. For areas of ecological significance land uses no increase in the level of protection is recommended (Schedule B5b) as the default level (that is, for non-biomagnifying contaminants) is already 99% protective of species. The methodology was adopted and the resulting SQG(NOEC & EC10) values are presented in Table 43.

Table 43. Soil quality guidelines based on no observed effect concentration and 10% effect concentration toxicity data (SQG(NOEC & EC10)) for DDT in freshly contaminated soils with different land uses.

Land use

SQG(NOEC & EC10)

(mg total DDT/kg soil)

Areas of ecological significance

1a

Urban residential/public open space

70b

Commercial/industrial

250c

a to protect 99% of species, b to protect 85% of species, c to protect 65% of species.

It should be noted that if a site-specific ABC for DDT is determined (and there is sufficient justification for this ABC to be used instead of the default value of 0 mg/kg) then it may be added to the above generic SQG(NOEC & EC10) values to obtain a site-specific SQG(NOEC & EC10). As the values in Table 43 are generic SQG(NOEC & EC10) values they should be applied to all Australian soils that have the particular land use.

The SQG(LOEC & EC30) and SQG(EC50) values were calculated using the same method as that for the corresponding values for Zn, As and naphthalene. The data used to calculate these SQGs is presented in Table 42. To maximise the data available to generate the SQG(LOEC & EC30) and SQG(EC50) values, the available toxicity data was converted to the appropriate measure of toxicity using the default conversion factors recommended in  Schedule B5b and presented in Table 30.

 

As with the SQG(NOEC & EC10) values for DDT, soil-specific SQG(LOEC & EC30) and SQG(EC50) values could not be generated, so rather a single generic SQG(LOEC & EC30) and SQG(EC50) was generated for each of the three land uses (Table 44). As these are generic SQGs, they should be applied to all Australian soils with the particular land use.


Table 44. Soil quality guidelines for DDT in freshly contaminated soil with different land uses based on lowest observed effect concentration and 30% effect concentration toxicity data, and based on 50% effect concentration toxicity data.

Land use

SQG(LOEC & EC30) (mg/kg total DDT)

SQG(EC50)

(mg/kg total DDT)

Areas of ecological significance

3

6

Urban residential/public open space

180

360

Commercial/industrial

640

1300

There is currently no ageing or leaching factor available for DDT and therefore SQGs for aged contamination could not be derived.

The DDT SQGs were considered to be of moderate reliability as the toxicity data set met the minimum data requirements to use an SSD method but there were no normalisation relationships available to account for soil characteristics (Schedule B5b).

The most common metabolites of DDT are shown in Table 45. DDE is a well-known metabolite of DDT and is relatively well studied. However, there is considerably less information available on the environmental fate, metabolism, degradation and toxicity of these metabolites than on DDT. The HILs and some soil quality guidelines use a sum of DDT, DDE and DDD concentration as an SQG , for example,  the Dutch and Flemish SQGs. An SQG could be derived for the sum of DDT, DDE and DDD by assuming the compounds have concentration-additive toxicity.

Table 45. Major metabolites of DDT (Sourced from WHO 1989).

Abbreviation of metabolite

Chemical name of metabolite

DDE

1,1'-(2,2-dichloroethenylidene)-bis[4-chlorobenzene]

TDE(DD)          

1,1'-(2,2-dichloroethylidene)-bis[4-chlorobenzene]

DDMU 

1,1'-(2-chloroethenyldene)-bis[4-chlorobenzene]

DDMS   

1,1'-(2-chloroethylidene)-bis[4-chlorobenzene]

DDNU   

1,1'-bis(4-chlorophenyl)ethlyene

DDOH 

2,2-bis(4-chlorophenyl)ethanol

DDA 

2,2-bis(4-chlorophenyl)-acetic acid

Methoxychlor

1,1'-(2,2,2-trichloroethylidene)-bis[4-methoxybenzene]

Perthane 

1,1'-(2,2-dichloroethylidene)-bis[4-ethylbenzene]

DFDT

1,1'-(2,2,2-trichloroethylidene)-bis[4-fluorobenzene]

 

Soil quality guidelines for DDT in a number of jurisdictions are presented in Table 46. These SQGs have a variety of purposes and levels of protection and therefore a comparison of the values is problematic. The SQGs for DDT range from 0.01 to 4 mg/kg total DDT, both from the Netherlands. The original NEPM  (NEPC 1999) did not include an EIL for DDT. However, there are four HIL values of 260, 700, 400 and 4,000 mg/kg for land use settings A, B, C and D[3] for the sum of DDT, DDD, and DDE (Schedule B1). The SQGs for urban residential/public open space soil contaminated with fresh DDT based on NOEC & EC10, LOEC & EC30, and EC50 data were 70, 170 and 350 mg/kg. These values are considerably higher than the SQGs from other jurisdictions and this reflects the different methods that are used to account for biomagnification. The SQG(NOEC and EC10) and SQG(LOEC & EC30) are approximately 27% and 67% respectively, of the HIL for the standard residential setting ( setting A) which assumes direct exposure and the consumption of some food grown on the contaminated soil. The SQGs should still offer a considerable degree of protection.

Table 46. Soil quality guidelines for DDT in a number of jurisdictions.

Name of the DDT soil quality guideline

Value of the guideline

(mg/kg as total)

Dutch target values1

0.01

Dutch intervention value1

4

Canadian SQG (residential)2

0.7

Eco-SSL plants3

NA

Eco-SSL soil invertebrates3

NA

Eco-SSL avian3

0.093

Eco-SSL mammalian3

0.021

EU potentially unacceptable (residential)4

14

1 = VROM 2000

2 = CCME 1999d, 2006 and http://www.ccme.ca/publications/list_publications.html#link2

3 = http://www.epa.gov/ecotox/ecossl/

4 = Carlon 2007

NA = not available

 

 

7                   Copper

The following compounds were considered in deriving the SQGs for Cu:

The two key considerations in determining the most important exposure pathways for inorganic contaminants are whether they biomagnify and whether they have the potential to leach to groundwater.

 

A surrogate measure of the potential for a contaminant to leach is its watersoil partition coefficient (Kd). If the logarithm of the Kd (log Kd) of an inorganic contaminant is less than 3, then it is considered to have the potential to leach to groundwater (Schedule B5b). The Australian National Biosolids Research Program measured the log Kd of Cu in 17 agricultural soils throughout Australia. These measurements showed that, in most soils, the log Kd of Cu was below 3 L/kg (unpublished data). The log Kd value for Cu reported by Crommentuijn et al. (2000) was 2.99 L/kg. Therefore, there is the potential for Cu in some soils to leach to groundwater and affect aquatic ecosystems. However, the methodology for SQG derivation (Schedule B5b) does not advocate the routine derivation of SQGs that account for leaching potential. Rather, it advocates that this be done on a site-specific basis as appropriate (Schedule B5b).

 

Copper is an essential element for the vast majority of living organisms and, as such, concentrations of Cu in tissue are highly regulated and it does not biomagnify (Louma & Rainbow 2008; Heemsbergen et al. 2008; EC 2008a). Therefore, the biomagnification route of exposure does not need to be considered for Cu and the SQGs will only account for direct toxicity.

The ecotoxicology of Cu has been extensively studied both within Australia and internationally. Most studies presented their toxicity data as an added concentration (that is, the concentration of the contaminant added to the soil that causes a specified toxic effect) or in a form that permitted the added concentration to be calculated (that is, by subtracting the background from the total concentration).

 

The toxicity database used to calculate the SQGs for Cu consisted of over 400 toxicity measures for 11 soil processes (Table 47), 10 invertebrate species (Table 48) and 18 plant species (Table 49). The raw data used to generate Tables 4749 is provided in Appendix E. There was sufficient data—that is, toxicity data for at least five species or soil processes that belong to at least three taxonomic or nutrient groups (Schedule B5b)available to derive SQGs using a species sensitivity distribution (SSD) methodology.

 

Given that Cu does not biomagnify, the level of protection recommended in the SQG derivation methodology for urban residential/public open space land is 80% (that is, 80% of species would be protected) (Schedule B5b).

 


Table 47. The lowest geometric mean values of the normalised copper (Cu) toxicity data (expressed in terms of added Cu) for soil microbial processes.

Soil process

Geometric means (mg/kg added Cu)

 

EC10 or NOEC

EC30 or LOEC

EC50

Ammonification

721

1081

2164

Denitrification

59.6

149

179

Glutamic acid decomposition

64.7

329

659

Maize residue mineralisation

199

299

597

Microbial biomass carbon

35.6

80.9

107

Microbial biomass nitrogen

141

90.9

174

N mineralisation

81

84

160

Potential nitrification rate

137

205

282

Respiration

151

916

3165

Substrate induced nitrification

276

421

700

Substrate induced respiration

86

224

589

 

Table 48. The lowest geometric mean values of the normalised copper (Cu) toxicity data (expressed in terms of added Cu) for soil invertebrate species.

Species

Geometric means

(mg/kg added Cu)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Earthworm

Eisenia andrei

44.3

66.5

133

Earthworm

Eisenia fetida

61.4

129

169

Earthworm

Lumbriculus rubellus

42.4

117

656

Mite

Hypoapsis aculeifer

195

293

586

Mite

Platynothrus peltifer

70.7

106

212

Nematode

Plectus acuminatus

27.6

86.4

259

Potworm

Cognettia sphagnetorum

36.2

61.7

94.6

Springtail

Folsomia fimetaria

265

398

630

Springtail

Folsomia candida

205

343

499

Springtail

Isotoma viridis

135

202

405

 


Table 49. The lowest geometric mean values of the normalised copper (Cu) toxicity data (expressed in terms of added Cu) for individual plant species.

Plant species

Geometric means

(mg/kg added Cu)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Annual meadow grass

Poa annua

99.4

90.2

140

Barley

Hordeum vulgare

47.5

74.6

187

Canola

Brassica napus

825

1157

1125

Cotton

Gossypium sp.

 

 

 

Groundsel

Senico vulgaris

27.8

56.4

87.7

Maize

Zea mays

 

 

 

Millet

Panicum milaceum

 

 

 

Oats

Avena sativa

147

221

442

Peanuts

Arachis hypogaea

 

 

 

Perennial ryegrass

Lolium perenne

69.5

374

690

Smooth hawkesbeard

Hypochoeris radicata

98.2

164

186

Sorghum

Sorghum sp.

 

 

 

Sugar cane

Sacharum sp.

 

 

 

Tomato

Lycopersicon esculentum

126

196

325

Triticale

Tritosecale sp.

 

 

 

Wheat

Triticum aestivum

 

 

 

Wild buckwheat

Polygonum convolvulus

124

196

169

Daisy family

Andryala integrifolia

75.5

105

127

A normalisation relationship is an empirical model that predicts the toxicity of a single contaminant to a single species using soil physicochemical properties (for example, soil pH and organic carbon content). Normalisation relationships are used to account for the effect of soil characteristics on toxicity data. Thus, when toxicity data is normalised the effect of soil properties on the toxicity should be removed, so the resulting toxicity data should more closely reflect the inherent sensitivity of the test species.

 

Eighteen normalisation relationships were reported in the literature for Cu toxicity and an additional two were derived as part of this study (Table 50), giving a total of 20 normalisation relationships. Six were developed for Australian soils (Broos et al. 2007; Warne et al. 2008a; Warne et al. 2008b) and fourteen have been derived for European soils (Oorts et al. 2006a; Rooney et al. 2006; Criel et al. 2008; EC 2008a). Eight of the relationships were for plants, six for soil invertebrates, and six for microbial functions (Table 50).

 

The choice of normalisation relationships to be used to normalise the toxicity data was based on (1) regional relevance, (2) whether they are based on field- or laboratory-based toxicity data; preference is given to field-based relationships as they provide better estimates of toxicity in the field (Warne et al. 2008b), (3) providing a conservative SQGnormalisation relationships with lower gradients will provide lower normalised toxicity values and thus lower SQGs (EC 2008a), (4) the quality of the relationship as indicated by the coefficient of determination ( r2), and (5) the number of species to which the relationships apply.

 

Thus, whenever there were appropriate Australian normalisation relationships, these were applied to Australian toxicity data and the same rule applied to European normalisation relationships.

 

Of the Australian relationships, number 1 was not used as an equivalent field-based relationship for Australian soils was available (relationship 3) and relationship 2 was not used as ultimately it is the amount of harvestable food that is most important when considering crops. The best relationship developed by Broos et al. (2007) for substrate induced nitrification, (SIN) (relationship 4) was based on EC50 and pH. However, to be consistent with all the other normalisation relationships developed, the data was re-analysed using the logarithm of the EC50 data, which resulted in relationship 5, used in this Schedule. Relationship 7 was not used as relationships not explaining at least 60% of the variation are not considered appropriate for normalisation (Warne et al. 2008b). Relationship 3 was used to normalise all the Australian plant toxicity data and relationship 5 was used to normalise all the Australian microbial process toxicity data.

 

Of the European relationships, 8 rather than 7 was used for barley as it contained fewer parameters and had a marginally higher r2 value. Relationship 11 was used for tomato rather than relationships 9 and 10, as Fe oxide content of soils was not reported in the vast majority of the toxicity data and as relationship 11 had a lower gradient than relationship 10. For E. Fetida, relationship 13 was used as it had a lower gradient than relationship 12. Similarly, relationship 16 for F. candida was used rather than relationships 14 or 15 as it had a lower gradient.

 

All the toxicity data for European plant species, apart from barley, was normalised using relationship 11 for tomato as it was the plant relationship with the lowest gradient. All the European invertebrate toxicity data was normalised using relationship 13 for E. fetida as it was the invertebrate relationship with the lowest gradient and relationship 18 for SIR was used to normalise all European microbial process toxicity data (except that for maize residue mineralisation and potential nitrification rate) as it was the microbial process relationship with the lowest positive gradient.

 

All the Cu toxicity data in Tables 4749 was normalised to its equivalent toxicity in the recommended Australian reference soil (Schedule B5b) (Table 6). Depending on the conditions under which the toxicity tests were conducted, the normalised toxicity data could be higher or lower in the reference soil compared to the original toxicity data in the test soil.

 


Table 50. Normalisation relationships for the toxicity of copper (Cu) to plants, soil invertebrates and soil processes. The relationships used to normalise the toxicity data are in bold.

Eqn no.

Species/soil process

Y parameter

X parameter(s)

Reference

Australian relationships

1

Triticum aestivum (wheat)

log EC10a (laboratory-based data)

0.98 log CECb – 2.97 EC + 2.01 (r2 adj = 0.79)

Warne et al. 2008a

2

T. aestivum (wheat)

log EC50 (field-based 8wk growth)

0.54 pHc – 0.16

(r2 adj = 0.85)

Warne et al. 2008b

3

T. aestivum (wheat)

log EC10 (field-based grain yield)

0.31 pHc + 1.05 log OC + 0.56 (r2 adj = 0.80)

Warne et al. 2008b

4

SIN

EC50

434 pHc – 1615

(r2 adj = 0.73)

Broos et al. 2007

5

SIN

log EC50

0.35 pHc + 0.84

(r2 adj = 0.72)

This study

6

SIR

EC50d

22 clay + 641

(r2 adj = 0.38)

Broos et al. 2007

Northern hemisphere relationships

7

Hordeum vulgare (barley)

log EC10a

0.403 log CECe + 0.42 OC + 0.809

(r2 adj = 0.63)

Rooney et al. 2006

8

H. vulgare (barley)

log EC50

1.06 log CECe + 1.42
(r2 = 0.66)

EC 2008a

9

Lycopersicon esculentum (tomato)

log EC10a

0.855 log CECe + 0.388 log Fe oxide – 0.047

(r2 adj = 0.72)

Rooney et al. 2006

10

L. esculentum (tomato)

log EC10a

0.99 log CECe, f

EC 2008a

11

L. esculentum (tomato)

log EC50

0.96 log CECe + 1.47
(r2 = 0.75)

EC 2008a

12

Eisenia fetida (earthworm)

log EC10

0.606 log CECe + 1.56             
(r2 = 0.65)

Criel et al. 2008

13

E. fetida (earthworm)

log EC50

0.58 log CECe + 1.85
(r2 = 0.75)

EC 2008a

14

Folsomia candida (collembola)

log EC10

1.16 log CECe + 1.1

(r2 = 0.54)

Criel et al. 2008

15

F. candida (collembola)

log EC50

0.96 log CECe + 1.63           
(r2 = 0.63)

EC 2008a

16

F. candida (springtail)

Log EC10

0.8475 log CECe + 1.499
(r2 = 0.56)

This study

17

F. fimetria (springtail)

Log EC10

0.7508 log CECe + 2.0868       (r2 = 0.63)

This study

18

SIR

log EC50

0.66 log OC + 1.96

(r2 = 0.57)

Oorts et al. 2006a

19

MRM

log EC20

-0.26 pHc + 4.05

(r2 = 0.52)

Oorts et al. 2006a

20

PNR

log EC50

1.06 log CECe + 1.41           
(r2 = 0.66)

Oorts et al. 2006a

a = normalisation relationships were also developed for the same combination of species and endpoint but for different measures of toxicity e.g. log EC50 and NOEC and using other soil physicochemical properties.

b = these CEC measurements were made using the ammonium acetate method (Rayment & Higginson 1992).

c = pH measured in 0.01 M calcium chloride (Rayment & Higginson 1992).

d = no statistically significant normalisation relationships could be derived for EC10 and EC10 SIR data (NBRP unpublished data).

e = these CEC measurements were made using the silver thiourea method (Chhabra et al. 1975).

f = the full normalisation relationship was not provided in EC (2008a) but as only the slope of the relationship is used in the normalising, the constant is not necessary. CEC = cation exchange capacity (cmolc/kg); OC = organic carbon content (%); MRM = maize residue mineralisation; PNR = potential nitrification rate; SIN = substrate induced nitrification, SIR = substrate induced respiration.

The distribution of the sensitivity of species and microbial processes to Cu is presented in Figure 7. Toxicity data for plants, soil processes and soil invertebrates was generally evenly spread in the species sensitivity distribution (SSD); however, the invertebrates did not have the same range of highly tolerant species as the other two organism groups. Nonetheless, the overall distribution of sensitivity to Cu was similar. Therefore, all the toxicity data was used to derive the ACLs and SQGs.

 

Figure 7. The species sensitivity distribution (plotted as a cumulative frequency against added copper (Cu) concentration) of soil processes, soil invertebrates and plant species to Cu.

 

As described earlier, SQGs were derived using three sets of toxicity dataNOEC and EC10, LOEC and EC30, and EC50 data.

The NOEC and EC10 toxicity data was normalised as outlined in Heemsbergen et al. (2008). Geometric means for each toxic end point (for example, mortality, reproduction, seedling emergence) for each species were calculated and the lowest geometric mean selected to represent the sensitivity of each species/microbial process. These lowest geometric means were entered into the BurrliOZ software (Campbell et al. 2000) and ACL(NOEC & EC10) values calculated that should theoretically protect 99, 80 and 60% of species/microbial processes. The resulting ACL(NOEC and EC10) values are only applicable to the Australian reference soil (Table 6). In order to generate soil-specific ACLs the normalisation relationships were applied to the ACL(NOEC & EC10) values in the reverse manner.

 

A complicating factor for Cu is that there are different soil physicochemical properties (that is, CEC, pH, OC and a combination of pH and log OC) that control the toxicity of Cu depending on the species or microbial process (Table 50). However, these can be rationalised down to two factors that control the ACL, namely CEC (measured using the silver thiourea method, Chhabra et al. 1975) and pH (measured in 0.01M CaCl2, Rayment & Higginson 1992) (see Appendix F for a detailed explanation of this rationalisation). Thus, there are two sets of ACL values for each land use type (that is, a set that vary with CEC and a second set that vary with pH). To determine the ACL that applies to a site, it is simply a matter of measuring the CEC and pH of the soil, looking up the tables for the appropriate ACL and then adopting the lower of the two ACL values. In the majority of cases the pH-based ACL values will limit how much Cu can be added to a soil when the soil pH is less than or equal to 6, while the CEC-based ACL values will limit the amount of Cu that can be added to a soil when the soil pH is greater than 6.

 

The ACL values for areas of ecological significance, urban residential/public open space and commercial/industrial land uses are presented in Tables 51 to 53, respectively.

Table 51. Soil-specific added contaminant limits (ACLs, mg/kg) based on no observed effect concentration (NOEC) and 10% effect concentration (EC10) toxicity data for fresh copper (Cu) contamination that theoretically protect at least 99% of soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a cation exchange capacity (CEC) ranging from 5 to 60 cmolc/kg and for an area of ecological significance land use. The lower of the CEC- or the pH-derived ACLs that apply to a soil is the ACL(NOEC & EC10) to be used.

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

10

20

25

25

25

25

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

7

15

20

30

65

90

 

Table 52. Soil-specific added contaminant limits (ACLs, mg/kg) based on no observed effect concentration (NOEC) and 10% effect concentration (EC10) toxicity data for fresh copper (Cu) contamination that theoretically protect at least 80% of soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a cation exchange capacity (CEC) ranging from 5 to 60 cmolc/kg and an urban residential/public open space land use. The lower of the CEC- or the pH-derived ACLs that apply to a soil is the ACL(NOEC & EC10) to be used.

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

30

60

65

65

70

70

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

20

40

60

85

170

250


Table 53. Soil-specific added contaminant limits (ACLs, mg/kg) based on no observed effect concentration (NOEC) and 10% effect concentration (EC10) toxicity data for fresh copper (Cu) contamination that theoretically protect at least 60% of soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a cation exchange capacity (CEC) ranging from 5 to 60 cmolc/kg and a commercial/industrial land use. The lower of the CEC- or the pH-derived ACLs that apply to a soil is the ACL(NOEC & EC10) to be used.

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

45

90

100

100

110

110

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

30

60

90

130

270

380

 

To convert ACL(NOEC & EC10) values to SQG(NOEC & EC10) values, the ambient background concentration (ABC) needs to be added to the ACL(NOEC & EC10). Three methods of determining the ABC were recommended in the methodology for deriving SQGs (Heemsbergen et al. 2008).

The preferred method is to measure the ABC at an appropriate reference site. However, where this is not possible, the methods of Olszowy et al. (1995) and Hamon et al. (2004) were recommended to predict the ABC where there has been and has not been, respectively, a history of contamination. In the Hamon et al. (2004) method, the ABC for a variety of metal contaminants, including Cu, vary with either the soil iron or manganese content. The equation to predict the ABC for Cu in soils with no history of Cu contamination (Hamon et al. 2004) is:

log Cu conc (mg/kg) = 0.612 log Fe content (%) + 0.808    (equation 7)

 

Examples of the ABC values predicted by this equation are presented in Table 54.

Table 54. Ambient background concentrations (ABCs) for copper (Cu) predicted using the Hamon et al. (2004) method.

Fe content (%)

Predicted Cu ABC (mg/kg)

0.1

2

0.5

4

1

6

2

10

5

15

10

25

15

35

20

40

 

Predicted ABC values for Cu range from approximately 2 to 40 mg/kg in soils with iron contents between 0.1 and 20%.

To calculate an SQG(NOEC & EC10), the ABC value is added to the ACL(NOEC & EC10). Ambient background concentration values vary with soil type. Therefore it is not possible to present a single set of SQGs. Thus, two examples of SQG(NOEC & EC10) values for urban settings are presented below. These examples would be at the low and high end of the range of SQG(NOEC & EC10) values (but not the extreme values) generated for Cu in Australian soils.

 

Example 1

Site descriptors urban residential/public open space land use in a new suburb (that is, fresh Cu contamination).

Soil descriptors – a sandy acidic soil (pH 5.5, CEC 10) with 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10)  values are:

ACL(NOEC & EC10) CEC-based:  60 mg/kg

ACL(NOEC & EC10) pH-based: 40 mg/kg

ACL(NOEC & EC10):   40 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:     6 mg/kg

SQG(NOEC & EC10):   46 mg/kg, (which would be rounded off to 45 mg/kg).

 

Example 2

Site descriptors commercial/industrial land use in a new suburb (that is, fresh Cu contamination).

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10) CEC-based:  110 mg/kg

ACL(NOEC & EC10) pH-based: 270 mg/kg

ACL(NOEC & EC10):   110 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:    25 mg/kg

SQG(NOEC & EC10):   135 mg/kg, which would be rounded off to 130 mg/kg.

In addition to calculating SQG(NOEC & EC10) values, Heemsbergen et al. (2008) suggested that two other sets of SQGs could be generated using either a combination of LOEC and EC30 data or EC50 data. These SQGs are termed the SQG(LOEC & EC30) and SQG(EC50) respectively. These additional SQGs were calculated using the method described in Heemsbergen et al. (2008) except the input data for the SSD was changed to the appropriate type (Table 1). The lowest geometric means of the normalised toxicity data used to generate these SQGs are presented in Tables 4749 and the raw data can be found in Appendix E. Lowest observed effect concentration, 30% effect concentration and 50% effect concentration toxicity data was not available in all instances; therefore, to maximise the data available to calculate SQG(LOEC & EC30) and SQG(EC50) values, the available NOEC and EC10 toxicity data was converted to these measures using conversion factors as necessary. The NBRP developed experimentally derived conversion factors (cited in Heemsbergen et al. 2008) for Cu and Zn (Table 17). These conversion factors were used rather than the generic conversion factors often used to convert toxicity data. This approach is consistent with the recommendation of Heemsbergen et al. (2008). Tables 55 and 56 show the soil-specific ACL(LOEC & EC30) and ACL(EC50) values respectively, for soils with areas of ecological significance, urban residential/public open space and commercial/industrial land uses.

Table 55. Soil-specific ACLs (mg/kg) based on lowest observed effect concentration (LOEC) and 30% effect concentration (EC30) data for fresh copper (Cu) contamination that should theoretically provide the appropriate level of protection (that is, 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a CEC ranging from 5 to 60 cmolc/kg for various land uses. The lower of the CEC- or the pH-derived ACLs for a particular land use that apply to a soil is the ACL(LOEC & EC30) to be used.

Areas of ecological significance land use

Type of ACL

CEC (cmolc/kg)a

 

5

10

20

30

40

60

CEC-based ACLs

25

50

50

55

55

60

 

pHb

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

15

30

50

70

140

200

Urban residential/public open space land use

Type of ACL

CEC(cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

50

100

110

110

120

120

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

30

70

100

140

290

420

Commercial/industrial land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

70

150

160

170

170

180

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

45

100

150

210

440

630

a = CEC was measured using the silver thiourea method (Chhabra et al. 1972).

b = pH was measured using the CaCl2 method (Rayment & Higginson 1992).


Table 56. Soil-specific ACLs (mg/kg) based on 50% effect concentration (EC50) data for fresh copper (Cu) contamination that should theoretically provide the appropriate level of protection (that is, 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a cation exchange capacity (CEC) ranging from 5 to 60 cmolc/kg for various land uses. The lower of the CEC- or the pH-derived ACLs for a particular land use that apply to a soil is the ACL(EC50) to be used.

Areas of ecological significance land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

35

75

85

85

90

95

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

25

50

75

110

230

320

Urban residential/public open space land use

Type of ACL

CEC

 

5

10

20

30

40

60

CEC-based ACLs

85

170

190

200

200

210

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

50

120

170

250

510

730

Commercial/industrial land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

125

260

280

290

310

320

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

80

180

260

380

770

1100

The ABC values were calculated using the method described earlier and the values presented in Table 54.

As the ACL and ABC values are both soil-specific it is not possible to generate a single set of SQGs. Example SQGs that represent values that at the upper and lower end of the range of values that would be encountered in urban situations are presented. Two examples are presented for SQGs based on LOEC and EC30 data and two examples based on EC50 data.


 

SQG(LOEC & EC30)Example 1

Site descriptors urban residential/public open space land use in a new suburb.

Soil descriptors – a sandy acidic soil (pH 5.5, CEC 10) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30) CEC-based:  100 mg/kg

ACL(LOEC & EC30) pH-based: 70 mg/kg

ACL(NOEC & EC10):   70 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:     6 mg/kg

SQG(LOEC & EC30):    76 mg/kg, which would be rounded off to 75 mg/kg.

 

SQG(LOEC & EC30)Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30) CEC-based:  170 mg/kg

ACL(LOEC & EC30) pH-based: 440 mg/kg

ACL(NOEC & EC10):   170 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:     25 mg/kg

SQG(LOEC & EC30):    195 mg/kg, which would be rounded off to 190 mg/kg.

 

SQG(EC50)Example 1

Site descriptors urban residential/public open space land use in a new suburb.

Soil descriptors – a sandy acidic soil (pH 5.5, CEC 10) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50) CEC-based:   170 mg/kg

ACL(EC50) pH-based:   120 mg/kg

ACL(EC50):    120 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:     6 mg/kg

SQG(EC50):    126 mg/kg ,which would be rounded off to 130 mg/kg.

 

SQG(EC50) -  Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50) CEC-based:   310 mg/kg

ACL(EC50) pH-based:   770 mg/kg

ACL(EC50):    310 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:     25 mg/kg

SQG(EC50):    335 mg/kg ,which would be rounded off to 330 mg/kg.

 

In addition to calculating SQGs in recently contaminated soils (that is, contamination is <2 years old), Heemsbergen et al. (2008) suggested that an identical set of SQGs could be derived for soils where the contamination is aged (that is, it has been present for ≥2 years). The Cu SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values for aged sites were calculated using the methods set out in earlier sections, the only difference being that laboratory toxicity data based on freshly spiked soils or soils that had not been leached were multiplied by an ALF (Schedule B5b). An ALF of 2 was developed by Smolders et al. (2009) while a value of 2.2 was developed and used in the EC ecological risk assessment for Cu (EC 2008a). Given the uniformity of these ALF values and to err on the conservative side (that is to offer greater protection to the environment), an ALF of 2 was adopted in this study.

The raw toxicity data (Appendix E) for Cu that was generated using freshly spiked and non-leached soils was multiplied by the ALF of 2. That data that was field-based and aged and/or leached laboratory-based data was not multiplied by the ALF. In all other ways the aged ACL(NOEC & EC10) and SQG(NOEC & EC10) values were calculated using the same methods as described in earlier sections. The resulting soil-specific ACL(NOEC & EC10) values for aged Cu contamination are presented in Table 57.

 

Table 57. Soil-specific ACLs (mg/kg) based on no observed effect concentration (NOEC) and 10% effect concentration (EC10) data for aged copper (Cu) contamination that should theoretically provide the appropriate level of protection (i.e., 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a CEC ranging from 5 to 60 cmolc/kg for various land uses. The lower of the CEC- or the pH-derived ACLs for a particular land use that apply to a soil is the aged ACL(NOEC & EC10) to be used.

Areas of ecological significance land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

15

25

30

30

30

35

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

8

20

25

40

80

110

Urban residential/public open space land use

Type of ACL

CEC

 

5

10

20

30

40

60

CEC-based ACLs

50

110

110

120

120

130

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

30

70

110

150

310

440

Commercial/industrial land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

80

160

180

180

190

200

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

50

110

160

230

480

680

 

For aged contaminated sites (that is, the contamination has been in place for at least 2 years) the  methodology (Schedule B5b) recommends using the 25th percentiles of the ABC data for the ‘old suburbs’ from Olszowy et al. (1995) (see Table 58).

Table 58. Copper (Cu) ambient background concentrations (ABC) based on the 25th percentiles of Cu concentrations in ‘old suburbs’ (that is, >2 years old) from various states of Australia (Olszowy et al. 1995).

Suburb type

25th percentile of Cu ABC values (mg/kg)

NSW

QLD

SA

VIC

Old suburb, low traffic

20

10

15

10

Old suburb, high traffic

30

15

25

10

SQGs are the sum of the ABC and ACL values, both of which are soil-specific. It is, therefore, not possible to present a single set of SQGs. Thus, some examples of SQG(NOEC & EC10) values for aged urban soils are provided below. These examples represent SQG(NOEC & EC10) values that would be at the low and high end of the range of SQG(NOEC & EC10) values that would be generated for Cu in Australian soils, but are not extreme values.

 

Example 1

Site descriptors – urban residential land /public open space use in an old Victorian suburb with low traffic volume.

Soil descriptors – a sandy acidic soil (pH 5.5, CEC 10) with 1% iron and aged Cu contamination and a low traffic volume.

The resulting aged ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

aged ACL(NOEC & EC10) CEC-based:  110 mg/kg

aged ACL(NOEC & EC10) pH-based:  70 mg/kg

aged ACL(NOEC & EC10 ):  70 mg/kg (the lower of the two ACLs that apply to this soil)

aged ABC:    10 mg/kg

aged SQG(NOEC & EC10):    80 mg/kg

 

Example 2

Site descriptors – commercial/industrial land use in an old South Australian suburb with a high traffic volume.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron and aged Cu contamination.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

aged ACL(NOEC & EC10) CEC-based:  190 mg/kg

aged ACL(NOEC & EC10) pH-based:  480 mg/kg

aged ACL(NOEC & EC10):   190 mg/kg (the lower of the two ACLs that apply to this soil)

aged ABC:    25 mg/kg

aged SQG(NOEC & EC10):    215 mg/kg, which would be rounded off to 210 mg/kg.

 

The ACL(LOEC & EC30) and ACL(EC50) values for aged Cu contamination were calculated in the same manner as the aged ACL(NOEC & EC10) values, except that LOEC and EC30 or EC50 toxicity data was used respectively. The aged ACL(LOEC & EC30) and aged ACL(EC50) values are presented in Tables 59 and 60 respectively.

Table 59. Soil-specific added contaminant limits (ACLs, mg/kg) based on LOEC and 30% effect concentration (EC30) data for aged copper (Cu) contamination that should theoretically provide the appropriate level of protection (i.e. 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a CEC ranging from 5 to 60 cmolc/kg for various land uses. The lower of the CEC- or the pH-derived ACLs for a particular land use that apply to a soil is the aged ACL(LOEC & EC30) to be used.

Areas of ecological significance land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

30

65

70

70

75

80

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

20

45

65

90

190

270

Residential urban /public open space land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

95

190

210

220

220

230

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

60

130

190

280

560

800

Commercial/industrial land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

140

280

300

320

330

340

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH-based ACLs

85

190

280

400

830

1200

 

Table 60. Soil-specific ACLs (mg/kg) based on 50% effect concentration (EC50) data for aged copper (Cu) contamination that should theoretically provide the appropriate level of protection (i.e. 99, 80 or 60% of species) to soil processes, soil invertebrate species and plant species in soils with a pH ranging from 4.5 to 8 and a CEC ranging from 5 to 60 cmolc/kg for various land uses. The lower of the CEC- or the pH-derived ACLs for a particular land use that apply to a soil is the aged ACL(EC50) to be used.

Areas of ecological significance land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

80

170

180

190

190

200

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH -based ACLs

50

110

170

240

490

700

Urban residential /public open space land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

150

300

350

350

350

400

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH -based ACLs

95

200

300

450

900

1300

Commercial/industrial land use

Type of ACL

CEC (cmolc/kg)

 

5

10

20

30

40

60

CEC-based ACLs

210

440

470

490

510

530

 

pH

 

4.5

5.5

6

6.5

7.5

8.0

pH -based ACLs

130

290

440

630

1300

1800

 

The ABC values for aged Cu contamination were calculated using the data from Olszowy et al. (1995), and are presented in Table 58.

Four examples of SQGs that would apply to aged Cu contamination that represent the range (but not the extremes) of SQGs that would apply to urban residential/public open space and commercial/industrial land uses are presented below.

SQG(LOEC & EC30)Example 1

Site descriptors urban residential land/public open space use in an old Victorian suburb with a low traffic volume.

Soil descriptors – a sandy acidic soil (pH 5.5, CEC 10) with 1% iron content.

The resulting aged ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

aged ACL(LOEC & EC30) CEC-based:  190 mg/kg

aged ACL(LOEC & EC30) pH-based: 130 mg/kg

aged ACL(LOEC & EC30): 130 mg/kg (the lower of the two ACLs that apply to this soil)

aged ABC:  10 mg/kg

aged SQG(LOEC & EC30):  140 mg/kg

 

SQG(LOEC & EC30)Example 2

Site descriptors commercial/industrial land use in an old South Australian suburb with a high traffic volume.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

aged ACL(LOEC & EC30) CEC-based: 330 mg/kg

aged ACL(LOEC & EC30) pH-based: 830 mg/kg

aged ACL(LOEC & EC30): 330 mg/kg (the lower of the two ACLs that apply to this soil)

aged ABC:  25 mg/kg

aged SQG(LOEC & EC30):  355 mg/kg, which would be rounded off to 350 mg/kg.

 

SQG(EC50)Example 1

Site descriptors urban residential land/public open space use in an old Victorian suburb with a low traffic volume.

Soil descriptors – a sandy acidic soil (pH 5.5, CEC 10) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50)  values are:

ACL(EC50) CEC based:  300 mg/kg

ACL(EC50) pH based:  200 mg/kg

ACL(EC50):  200 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:  10 mg/kg

SQG(EC50):  210 mg/kg

 

 

SQG(EC50)Example 2

Site descriptors commercial/industrial land use in an old South Australian suburb with a high traffic volume.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with a 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50) CEC based:   510 mg/kg

ACL(EC50) pH based:   1300 mg/kg

ACL(EC50):    510 mg/kg (the lower of the two ACLs that apply to this soil)

ABC:     25 mg/kg

SQG(EC50):    535 mg/kg, which would be rounded off to 530 mg/kg.

 

Based on the criteria established in the methodology for SQG derivation (Schedule B5b), all the Cu  SQGs were considered to be of high reliability. This resulted as the toxicity data set easily met the minimum data requirements to use the SSD method and there were normalisation relationships available to account for soil characteristics.

A compilation of SQGs for Cu from a number of jurisdictions is presented in Table 61. These SQGs have a variety of purposes and levels of protection and therefore comparison of the SQGs amongst each other and with the Cu SQGs is problematic. As well, the vast majority of the international SQGs are not soil-specific nor do they account for ageing and leaching. One would therefore expect that the ACLs could be higher than other internationals SQGs. The international guidelines for Cu range from 14 to 1,000 mg/kg (added or total Cu) both being from member countries of the European Union (Carlon 2007). The superseded interim urban EIL (NEPC 1999) for Cu was 100 mg/kg total Cu and therefore in the middle of the range of the international Cu guidelines.

 

Overall, the superseded interim urban EIL lies in the lower to middle part of the range of ACLs for fresh Cu contamination, while the superseded interim urban EIL lies at the lower third of the range of ACLs for aged contamination.

 

All of the soil-specific ACL values for urban residential land/public open space land use (irrespective of the toxicity data on which they were based) fell within the range of the international residential SQGs, the one exception being the ACLs based on EC50 for soils where the Cu has low bioavailability (that is, high pH and high CEC), which were greater than 1,000 mg/kg added Cu.

 

However, this was a CEC-based ACL and, as stated earlier, when the soil pH is greater than 6, the pH-based ACLs will limit the amount of Cu that can be present in soil. When this was taken into account, all the soil-specific ACL values for residential land use fell within the range of international SQGs.

 

Similarly, all the ACLs for commercial/industrial land use, with the exception of the aged ACLs based on EC50, fell within the range of international SQGs for Cu. The one exception was the ACL(EC50) value that would permit concentrations nearly twice (that is, 1,800 mg/kg added) that of the collated international limits (1,000 mg/kg). However, in soils with a pH above 6, the pH-based ACL will limit the amount of Cu that is permitted in soil and thus all the ACLs for commercial/industrial land use fell within the range of international SQGs.

 

The  Cu ACL(NOEC & EC10) values in freshly contaminated urban residential/public open space soils (which should theoretically protect 80% of species) ranged from 20 to 250 mg/kg (added Cu) (Table 53). The most suitable comparison with these values is with the limits recommended by the EC Cu ecological risk assessment which used NOEC and EC10 data and should theoretically protect 95% of species. These values range from 20 to 173 mg/kg added Cu. The limits derived by these two processes are very similar.

Table 61. Soil quality guidelines for copper (Cu) from international jurisdictions.

Name of Cu limit

Numerical value of the limit (mg/kg)

Dutch target value1

36 (added Cu)

Dutch intervention level1

190 (added Cu)

Canadian SQG (residential)2

63 (total Cu)

Canadian SQG (commercial and industrial)2

91 (total Cu)

Eco-SSL plants3

70 (total Cu)

Eco-SSL soil invertebrates3

80 (total Cu)

Eco-SSL avian3

28 (total Cu)

Eco-SSL mammalian3

49 (total Cu)

EU minimal risk values (residential)4

1470 (added and total Cu)

EU warning risk values (residential)4

100500 (added and total Cu)

EU potential risk values (residential)4

1001000 (added and total Cu)

EU Cu ecological risk assessment5

26176 (added Cu)

1 = VROM 2000

2 = CCME 1999e, & 2006 and http://ceqg-rcqe.ccme.ca/

3 =  http://www.epa.gov/ecotox/ecossl/

4 = Carlon 2007

5 = EC 2008a.

 

8                   Lead

The following compounds were considered in deriving the SQGs for lead (Pb):

If the logarithm of the Kd (log Kd) of an inorganic contaminant is less than 3 then it is considered to have the potential to leach to groundwater (Schedule B5b). The log Kd reported by Commentuijn et al. (2000) for Pb was 3.28 L/kg so there is little potential for Pb to leach to groundwater. If this exposure pathway were considered important at a site, then the methodology for SQG derivation advocates that this be addressed on a site-specific basis as appropriate (Schedule B5b).

 

The bioconcentration, bioaccumulation and biomagnification of Pb in aquatic ecosystems have received considerable attention. There has also been considerable attention paid to bioconcentration in terrestrial ecosystems but the biomagnification work has been more limited and often restricted to only examining transfer from food to consumer and not subsequent steps up food chains. One hundred and one terrestrial bioaccumulation factor (BAF) values for Pb have been published (LDA 2008) and these range from 0.00 to 6.86 with a median value of 0.1 kgdw/kgww (where dw = dry weight and ww = wet weight). The EU ecological risk assessment for Pb (LDA 2008) followed the EU technical guidance document (EC 1996), which applies assessment factors to the lowest NOEC for oral exposure of birds and mammals to account for the potential of Pb to biomagnify. However, using this method led to the derivation of limits that were below the concentrations found in control foods (that is, food that would occur in soils with background concentrations of Pb). These limits therefore imply that food (animal or plant) grown in soils with background concentrations poses a risk, which is not consistent with real-world experience. They therefore used an SSD method to determine the predicted no-effect concentration (PNEC) for oral exposure of birds and mammals and obtained a soil limit of 491 mg/kg. This value was higher than the limit based on direct exposure of soil organisms of 333 mg/kg.

 

Thus, it is apparent that Pb does not pose a biomagnification risk to terrestrial ecosystems. This finding is consistent with the findings for aquatic ecosystems that Pb does not biomagnify (Eisler 1988; Suedel et al. 1994; Demayo et al. 1982; Vighi 1981; Lu et al. 1975;  Henney et al. 1991) and is the conclusion reached by the EU Pb ecological risk assessment (LDA 2008). Therefore, only direct toxic effects to soil organisms were considered in the derivation of the SQGs.

All the available Pb toxicity data was reported with both the total concentration and ambient background concentration, therefore the data could be converted to added concentrations. A total of ninety-six toxicity measures were available for Pb. These were for eight plant species, five species of soil invertebrates and six microbial processes (Table 62). Thus, this met the minimum data requirements recommended by Heemsbergen et al. (2008) to use the BurrliOZ SSD method (Campbell et al. 2000). Table 62 shows the geometric means of toxicity values of each species or soil microbial process that were used to derive the SQGs for Pb. The raw toxicity data used to generate the species geometric means is presented in Appendix G. In the vaxt majority of cases the geometric means of the toxicity data increase from NOEC or EC10 to LOEC or EC30 to EC50 values. However, for F. candida, Raphanus sativa, A. sativa, P. tedea and L. Sativa, the EC50 values were lower than the LOEC and EC30 data. This reflects the fact that the Pb toxicity data was not normalised for soil properties and the toxicity tests were conducted in soils with a variety of physicochemical properties.

 

In order to maximise the use of the available toxicity data, conversion factors recommended in Schedule B5b to permit the inter-conversion of NOEC, LOEC, EC50, EC30 and EC10 data were used (Table 17).

Table 62. Geometric means of the toxicity of lead (Pb) (expressed in terms of added Pb) to soil invertebrates, plants and soil microbial processes.

Test species

Geometric mean (mg/kg)

Common name

Scientific name

NOEC or EC10

LOEC or EC30

EC50

Invertebrates

Earthworm

Dendrobaena rubida

129

194

387

Earthworm

Eisenia andrei

-

1500

3410

Earthworm

E. fetida

761

2026

3829

Earthworm

L. rubellus

1000

1500

3000

Springtail

F. candida

1797

3749

1866

Microbial processes

Soil process

ATP

-

-

3018

Soil process

Denitrification

250

500

750

Soil process

Nitrification

337

505

1010

Soil process

N-mineralisation

447

1095

1342

Soil process

Respiration

655

982

1964

Soil process

Substrate induced respiration

1733

2600

5200

Plants

Radish

Raphanus sativus

100

500

300

Oat

A. sativa

100

500

300

Barley

H. vulgare

50

250

1270

Red spruce

Picea rubens

141

212

1228

Loblolly pine

Pinus taeda

546

819

659

Lettuce

Latuca sativa

125

188

174

Wheat

T. aestivum

250

500

750

Maize

Z. mays

100

150

300

 

Only two normalisation relationships have been developed for Pb. One models the uptake of Pb by spring wheat (T. aesitivum) (Nan et al. 2002) while the other models Pb toxicity to lettuce (L. sativa) (Hamon et al. 2003). The toxicity normalisation relationship is presented below:

EC50 = 23 pH + 171 clay content (%) - 40  (r2 = 0.84)   (equation 8)

However, while the above relationship is based on ten toxicity data sets, they were only tested in five soils. This, combined with the fact that the relationship was not validated, severely limits its applicability. The EU ecological risk assessment for Pb (LDA 2008) stated that there is no relationship between soil pH and Pb toxicity. However, it did not make any statement on whether there are relationships between Pb toxicity and other soil physicochemical properties. This was examined as part of this body of work. Relationships between the logarithm of NOEC and/or EC10 data and soil pH, log organic matter content (%), log organic carbon content (%), log clay content (%) and log cation exchange capacity (CEC) for all toxicity data combined, for plants only, for invertebrates only and for soil microbial processes only were determined (data not shown). Normalisation relationships were only derived using NOEC and EC10 data as there was considerably more of this data than LOEC and EC30 or EC50 data. Only the relationship between logarithm of Pb toxicity to plants and the logarithm of the organic carbon content was able to explain more than 50% of the variation in toxicity data (r2 = 0.56).

 

Normalisation relationships that explain such a low percentage of the variation (that is, <60%) are not usually used to normalise toxicity data as they do not account for enough of the variability caused by the soil (Warne et al. 2008b). The majority of the relationships derived explained less than 10% of the variation in toxicity data and only three could explain more than 10%. Thus there are no useful normalisation relationships available for Pb, so the toxicity data was not normalised to the Australian reference soil, nor were soil-specific SQGs derived.

The SSD for the Pb NOEC toxicity data is presented in Figure 8. There was only toxicity data for 19 different species/microbial processes and the available data has not been normalised; therefore, the distribution reflects the variability in sensitivity of the organisms and the effect of soil properties. There was insufficient data to make a robust assessment of the relative sensitivity of the groups of organisms. However, the distributions of all three types of organisms overlap, so it was considered appropriate to use all the toxicity data to derive the SQGs.

Figure 8. The species sensitivity distribution of fresh lead (Pb) contamination (plotted as a cumulative frequency of the Pb NOEC toxicity data against soil Pb concentration) for soil invertebrates, plants and microbial processes.

There was NOEC and EC10, LOEC and EC30, and EC50 Pb toxicity data so ACLs and SQGs could be derived using each of these datasets. These were generated using the same general methods as for Cu.

There were no normalisation relationships available for Pb and therefore the NOEC and EC10 toxicity data was not normalised, nor could soil-specific ACL values be derived. The single numerical output from the SSD analysis for each land use became the generic (not soil-specific) ACL for that land use and these are presented in Table 63.

 

Table 63. Generic ACL (mg/kg) values based on NOEC and 10% effect concentration toxicity data (EC10) for fresh lead (Pb) contamination in soil with various land uses.

Land use

ACL(NOEC & EC10) (mg/kg)

Areas of ecological significance

40

Urban residential/public open space

130

Commercial/industrial

220

For sites with no history of contamination, the method of Hamon et al. (2004) is recommended to estimate the ABC. The equation to predict the Pb ABC is

 

log Pb conc (mg/kg) = 1.039 log Fe content (%) + 0.118    (equation 9)

 

Examples of the ABC values predicted by this equation are presented in Table 64. Predicted ABC values for Pb range from approximately 0.1 to 30 mg/kg in soils with iron concentrations between 0.1 and 20%.

Table 64. Lead (Pb) ABCs predicted using the method of Hamon et al. (2004) (see equation 9 above).

Fe content (%)

Predicted ABC (mg/kg)

0.1

0.1

0.5

0.6

1

1

2

3

5

7

10

15

15

20

20

30

The ABC values for Pb vary with the iron content of the soil. Therefore, it is not possible to present a specific set of SQGs(NOEC & EC10), but rather two examples of the range of SQGs that will be encountered in urban settings are presented.

Example 1

Site descriptors urban residential land/public open space use in a new suburb (i.e. fresh contamination).

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   130 mg/kg

ABC:     1 mg/kg

SQG(NOEC & EC10):   131 mg/kg, which would be rounded off to 130 mg/kg.

 

Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   220 mg/kg

ABC:    15 mg/kg

SQG(NOEC & EC10):   235 mg/kg, which would be rounded off to 230 mg/kg.

 

ACLs based on LOEC and EC30 toxicity data (ACL(LOEC & EC30)) and based on EC50 data (ACL(EC50)) were calculated using the method used to derive the ACL values based on NOEC and EC10 data, the one exception being that in order to maximise the amount of LOEC and EC30 and EC50 data, actual measured NOEC data was used to estimate LOEC, EC30 and EC50 data. This was done using the conversion factors derived by Heemsbergen et al. (2008) and presented in Table 17. The geometric means of the LOEC and EC30 data and of the EC50 data for the various species/microbial processes that were used to derive the ACL(LOEC & EC30) and  ACL(EC50) are presented in Table 62.

 

The resulting ACL(LOEC & EC30) and ACL(EC50) values for the three land uses are presented in Table 65. As expected, these values are larger than the corresponding ACL(NOEC & EC10) values. The ACL(EC50) values are also generally larger than the ACL(LOEC & EC30) values, with the exception of the values for areas of ecological significance. This occurs because the slope of the SSD for the LOEC and EC30 data is less than that of the EC50 data, the SSDs intersect and the LOEC and EC30 data ends up having larger toxicity values.

Table 65. Generic ACLs (mg/kg) based on LOEC and 30% effect concentration data (EC30) and based on 50% effect concentration data (EC50) values for fresh lead (Pb) contamination in soil with various land uses.

Land use

ACL(LOEC & EC30)

(mg/kg)

ACL(EC50)

(mg/kg)

Areas of ecological significance

110

60

Urban residential/public open space

270

490

Commercial/industrial

440

890

The ABC values for Pb were calculated using the Hamon et al. (2004) method as outlined previously.

As stated previously, the ABC values for Pb vary with the iron content of the soil. Therefore it is not possible to present a specific set of SQG (LOEC & EC30) or SQG (EC50) values. Four examples of SQGs that would apply to aged Pb contamination that represent the range (but not the extremes) of SQGs that would apply to urban residential/public open space and commercial/industrial land uses are presented below.

SQG(LOEC & EC30) Example 1

Site descriptors urban residential land/public open space use in a new suburb (that is, fresh contamination).

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    270 mg/kg

ABC:     1 mg/kg

SQG(LOEC & EC30):    271 mg/kg, which would be rounded off to 270 mg/kg.

 

SQG(LOEC & EC30) Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    440 mg/kg

ABC:    15 mg/kg

SQG(LOEC & EC30):    455 mg/kg, which would be rounded off to 450 mg/kg.

 

SQG(EC50) Example 1

Site descriptors urban residential land/public open space use in a new suburb (that is, fresh contamination).

Soil descriptors – a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    490 mg/kg

ABC:     1 mg/kg

SQG(EC50):    491 mg/kg, which would be rounded off to 490 mg/kg.

 

SQG(EC50) Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors – an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    890 mg/kg

ABC:    15 mg/kg

SQG(EC50):    905 mg/kg, which would be rounded off to 900 mg/kg.

 

Smolders et al. (2009) examined the literature and developed ALFs for Pb for a range of different organisms. The resulting ALFs ranged from 1.1 to 43 with a median of 4.2. The value of 4.2, recommended by Smolders et al. (2009), was adopted and used in the EU ecological risk assessment of Pb (LDA 2008). Leaching factors for Pb have been developed for five Australian soils from South Australia, which ranged from 0.92 to 2.98 and a median and geometric mean of 1.66 and 1.61 respectively (Stevens et al. 2003).

 

Given the values of Stevens et al. (2003) only account for leaching and not ageing, it is likely any ALFs for Australian soils would be larger and therefore are likely to be consistent with the ALF of Smolders et al. (2009). An ALF of 4.2 was adopted in this project to calculate the SQGs for aged Pb contamination.

The ACL values for aged contamination were calculated in exactly the same manner as those for fresh contamination except that the NOEC and EC10 toxicity data was corrected using the Smolders et al. (2009) ALF of 4.2. The resulting ACL values are presented in Table 66.

Table 66. Generic ACLs (mg/kg) based on NOEC data and 10% effect concentration data (EC10) for aged lead (Pb) contamination in soil with various land uses.

Land use

ACL(NOEC & EC10)

(mg/kg)

Areas of ecological significance

170

Urban residential/public open space

530

Commercial/industrial

940

 

For aged contaminated sites (that is, the contamination has been in place for at least 2 years), the methodology (Schedule B5b) recommends using the 25th percentiles of the ABC data for the ‘old suburbs’ from Olszowy et al. (1995) (see Table 67).

Table 67: Lead (Pb) ABCs based on the 25th percentiles of Pb concentrations in ‘old suburbs’ (i.e. >2 years old) from various states of Australia (Olszowy et al. 1995).

Suburb type

25th percentile of Pb ABC values (mg/kg)

NSW

QLD

SA

VIC

Old suburb, low traffic

100

30

30

35

Old suburb, high traffic

160

150

90

70

 

As the ABC values for Pb vary with the geographical location of the site it is not possible to present a single set of SQG(NOEC & EC10) values. Instead, two examples of the range of SQGs that will be encountered in urban settings are presented below.

Example 1

Site descriptors urban residential land/public open space use in an old South Australian suburb (that is, contamination is >2 years old), with low traffic volume.

Soil descriptors – these are not relevant as soil properties are not considered in determining the ACL for Pb.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   530 mg/kg

ABC:     30 mg/kg

SQG(NOEC & EC10):   560 mg/kg

 

Example 2

Site descriptors commercial/industrial land use in an old Queensland suburb (that is, contamination is >2 years old), with high traffic volume.

Soil descriptors – these are not relevant as soil properties are not considered in determining the ACL for Pb.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   940 mg/kg

ABC:    150 mg/kg

SQG(NOEC & EC10):   1090 mg/kg, which would be rounded off to 1100 mg/kg.

 

The ACL(LOEC & EC30) and ACL(EC50) values for aged Pb contamination were calculated using the method explained earlier, except that the data was multiplied by an ALF of 4.2 (Smolders et al. 2009). The resulting ACL(LOEC & EC30) and ACL(EC50) values for aged Pb contamination in the three land uses are presented in Table 68. As expected, these values are larger than the corresponding ACLs for fresh Pb contamination (Table 65).

Table 68: Generic ACLs based on LOEC and 30% effect concentration (EC30) toxicity data and based on 50% effect concentration toxicity data (EC50) values for aged lead (Pb) contamination in soil with various land uses.

Land use

ACL(LOEC & EC30)

(mg/kg)

ACL(EC50)

(mg/kg)

Areas of ecological significance

470

250

Urban residential/public open space

1100

2000

Commercial/industrial

1800

3700

 

The ABC values for aged Pb contamination were calculated using the method described earlier in this Schedule.

Four examples of SQGs that would apply to aged Pb contamination that represent the range (but not the extremes) of SQGs that would apply to urban residential/public open space and commercial/industrial land uses are presented below.


 

SQG(LOEC & EC30) Example 1

Site descriptors urban residential land/public open space use in an old South Australian (that is, contamination is >2 years old), with low traffic volume.

Soil descriptors these are not relevant as soil properties are not considered in determining the ACL for Pb.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    1100 mg/kg

ABC:     150 mg/kg

SQG(LOEC & EC30):    1250 mg/kg, which would be rounded off to 1,200 mg/kg.

 

SQG(LOEC & EC30) Example 2

Site descriptors commercial/industrial land use in an old Queensland suburb (that is, contamination is >2 years old), with high traffic volume..

Soil descriptors these are not relevant as soil properties are not considered in determining the ACL for Pb.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    1800 mg/kg

ABC:    150 mg/kg

SQG(LOEC & EC30):    1950 mg/kg, which would be rounded off to 1900 mg/kg,

 

SQG(EC50) Example 1

Site descriptors urban residential land/public open space use in an old South Australian (that is, contamination is >2 years old), with low traffic volume.

Soil descriptors these are not relevant as soil properties are not considered in determining the ACL for Pb.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):   2000 mg/kg

ABC:    30 mg/kg

SQG(EC50):   2030 mg/kg, which would be rounded off to 2000 mg/kg.

 

SQG(EC50) Example 2

Site descriptors commercial/industrial land use in an old Queensland suburb (that is, contamination is >2 years old), with high traffic volume.

Soil descriptors these are not relevant as soil properties are not considered in determining the ACL for Pb.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):   3700 mg/kg

ABC:   150 mg/kg

SQG(EC50):   3850 mg/kg, which would be rounded off to 3800 mg/kg.

 

The Pb toxicity data set met the minimum data requirements to use the SSD method but there were no suitable normalisation relationships available to account for soil characteristics. Based on the criteria for assessing the reliability of SQGs (Schedule B5b), this means that the Pb SQGs were considered to be of moderate reliability.

A compilation of SQGs for Pb in a number of jurisdictions is presented in Table 69. These SQGs have a variety of purposes and levels of protection and therefore comparison of the values is problematic. The superseded interim urban EIL for Pb was 600 mg/kg total.

 

The urban residential/public open space ACLs for fresh Pb contamination (irrespective of the type of toxicity data on which they were based) are all lower than the superceded interim urban EIL.

 

The aged ACL(NOEC & EC10) for urban residential land/public open space land use, at 530 mg/kg added, is lower than the superseded interim urban EIL, while the aged ACL(LOEC & EC30) and ACL(EC50) are considerably larger (1100 and 2000 mg/kg respectively). The ACL(NOEC & EC10) for fresh Pb contamination is similar to the Canadian residential SQG and the plant Eco-SSL (Table 69).

 

The fresh ACL(NOEC & EC10), ACL(LOEC & EC30) and ACL(EC50) for urban residential land/public open space land use correspond to the minimal, warning and potential risk values for residential land use of the EU. The fresh ACL(NOEC & EC10) is about 50% larger than the highest minimal risk SQG, but the ACL(LOEC & EC30) and ACL(EC50) lie within the range of values for the corresponding EU SQGs.

 

The best comparison (in terms of the way in which the SQGs were derived) with the ACLs   is with the limit derived by the EU ecological risk assessment for Pb (LDA 2008), which also corrected laboratory toxicity data for ageing and leaching. The EU derived a concentration that should protect 95% of terrestrial species of 333 mg/kg added Pb (LDA 2008). If the data and method that were used here (Schedule B5b) were used to calculate the concentration that should protect 95% of species, the value would be 275 mg/kg added Pbthis is slightly more conservative than the EU value.

 

Table 69. Soil quality guidelines for lead (Pb) in a number of international jurisdictions.

Name of the Pb soil quality guideline

Value of the guidelines (mg/kg)

Canadian SQG (residential)1

140 (total Pb)

Canadian SQG (commercial)1

260 (total Pb)

Canadian SQG (industrial)1

600 (total Pb)

Eco-SSL plants3

120 (total Pb)

Eco-SSL soil invertebrates3

1700 (total Pb)

Eco-SSL avian3

11 (total Pb)

Eco-SSL mammalian3

56 (total Pb)

Netherlands (target value)

85 (added Pb)

Netherlands (intervention value)

530 (added Pb)

EU minimal risk values (residential)2

2585 (added Pb)

EU warning risk values (residential)2

40700 (added Pb)

EU potential risk values (residential)2

100700 (added Pb)

EC Pb ecological risk assessment (aged HC5)4

333 (added Pb)

1 = CCME 1999f, 2006 and http://ceqg-rcqe.ccme.ca/

2 = Carlon 2007

3 = <http://www.epa.gov/ecotox/ecossl/>

4 = LDA 2008.

9                   Nickel

The following salts were considered in deriving SQGs for nickel (Ni):

For the leaching to groundwater pathway, adsorption (Kd) is the critical parameter. If the logarithm of the Kd (log Kd) of an inorganic contaminant is less than 3 then it is considered to have the potential to leach to groundwater (Schedule B5b). The log Kd reported by Commentuijn et al. (2000) for Ni was 2.08 L/kg, therefore there is some potential for Ni to leach to groundwater. If this exposure pathway was considered important for a given site, the methodology for SQG derivation advocates that this be addressed on a site-specific basis as appropriate (Schedule B5b).

 

The literature assessing the potential for Ni to biomagnify is limited, particularly for terrestrial ecosystems. However, all the available literature suggests that Ni does not biomagnify (Outridge & Schuehammer 1993; Torres & Johnson 2001; Campbell et al. 2005; Muir et al. 2005; Lapointe & Couture 2006). The EU ecological risk assessment for Ni also concluded that Ni did not biomagnify (EC 2008b). Therefore only direct toxic effects were considered in deriving the SQGs for Ni.

The raw toxicity data available for Ni is presented in Appendix H. There was a total of 338 toxicity measures for Ni. There was toxicity data for 11 plants species, 6 species of invertebrates and 26 microbial processes. The lowest geometric means of the toxicity data for each species and soil process are presented in Tables 70 and 71 respectively. This data exceeded the minimum data requirements to use the BurrliOZ software (Campbell et al. 2000) that is recommended in Schedule B5b. Therefore the SSD approach was used to derive the SQGs for Ni.

Table 70. The lowest geometric mean values of the normalised nickel (Ni) toxicity data for soil invertebrate and plant species.

Test species

Geometric means (mg/kg)

Common name

Scientific name

NOEC or EC10

LOEC or EC30

EC50

Invertebrates

Earthworm

E. fetida

162

245

474

Earthworm

Eisenia veneta

103

365

409

Earthworm

L. rubellus

407

523

575

Potworm

Enchytraeus albidus

134

239

205

Springtail

F. fimetaria

210

315

631

Springtail

F. candida

235

359

680

Plants

Alfalfa

Medicago sativa

36.4

80.8

87.1

Barley

H. vulgare

166.7

250

409

Fenugreek

Trigonella poenumgraceum

68.6

109

144

Lettuce

L. sativa

52.6

125

154

Maize

Z. mays

49.4

94.8

127

Oats

A. sativa

55.3

83.9

122

Onion

Allium cepa

37.6

59.7

84.5

Perennial ryegrass

L. perenne

40.9

50.2

57.1

Radish

R. sativus

57.5

65.5

66.8

Spinach

Spinacia oleracea

26.9

41.1

47.2

Tomato

L. esculentum

94.8

142

238

 

Table 71. The lowest geometric mean values of the normalised nickel (Ni) toxicity data for soil microbial processes.

Microbial process

Geometric means (mg/kg)

NOEC or EC10

LOEC or EC30

EC50

Arylsulfatase

784

1176

1191

Aspergillus clavatus (hyphal growth)

14.9

45.9

91.0

Aspergillus flavus (hyphal growth)

451

586

689

Aspergillus flavipes (hyphal growth)

398

444

475

Aspergillus niger (hyphal growth)

459

545

606

ATP content

75.5

113

392

Gliocladium sp. (hyphal growth)

230

560

1036

Bacillus cereus (colony count)

327

1010

1958

Dehydrogenase

6.8

20.8

85.5

Glucose respiration

79.5

119

238

Glutamate respiration

44.5

191

381

Maize residue respiration

134

201

402

Nitrification

81.3

122

244

N-mineralisation

95.8

144

287

Nocardia rhodochrous (colony count)

203

662

943

Penicillium vermiculatum (hyphal growth)

117

271

460

Phosphatase

524

1347

5715

Protease

75.5

113

392

Proteus vulgaris (colony count)

17.2

88.8

249

Respiration (CO2 release)

102

2583

4593

Rhizopus stolonifer (hyphal growth)

331

404

459

Rhodotorula rubra (colony count)

283

837

1796

Sacharase

75.5

113

392

Serratia marcescens (colony count)

178

337

395

Trichoderma viride (hyphal growth)

608

686

740

Urease

222

332

879

 

Normalisation relationships relating the toxicity of Ni to three soil microbial processes (nitrification, glucose-induced respiration and maize residue mineralisation) were developed by Oorts et al. (2006b). Two normalisation relationships have also been developed for crops (tomato and barley) by Rooney et al. (2007). In addition, the EU Ni ecological risk assessment (EC 2008b) reported Ni normalisation relationships for two soil invertebrates (F. candida and E. fetida). All of these relationships were developed for both fresh and aged contamination and are presented in Table 72. No Ni normalisation relationships have been developed for Australian species and/or soils.

 

The normalisation relationships presented in Table 72 all model EC50 toxicity data, with the exception of the maize residue mineralisation which models EC20 data. Relationships between the logarithm of Ni NOEC and EC10 data and logarithm of CEC were developed as part of this project. Normalisation relationships were developed for (a) all organisms, (b) each group of organisms separately, and (c) each species or microbial process separately. Only CEC was used to develop the normalisation relationships as in all the published relationships for Ni the CEC was the best parameter (Oorts et al. 2006b; Rooney et al. 2007; EC 2008b). Only six normalisation relationships could explain more than 50% of the variation in the toxicity data (i.e. r2 > 0.5) and these are presented in Table 73. The majority of the normalisation relationships had r2 values of <0.1.

 

Normalisation relationships are available for a variety of biological end points based on both NOEC and EC10 data and on EC50 data. The relationships used to normalise the data in the current study were relationships 1, 5 and 9 from Table 72 for glucose-induced respiration, nitrification and tomato, and relationships 2, 3, 5, 6 from Table 73 for barley, all invertebrates, maize residue mineralisation and respiration. The relationships with the lowest gradients for each species were selected. The exception to this was the relationship for invertebrates. This was selected as it was based on all invertebrate species and its gradient was only marginally higher than the invertebrate relationship with the lowest gradient. For the species that did not have normalisation relationships, the relationship for the most closely related species was used, or in the case where there were relationships for several related species, the relationship with the lowest gradient was used. Thus, all plant species (apart from tomato) were normalised with the EC10 relationship for barley and all the microbial processes without a relationship were normalised with the EC10 relationship for maize residue mineralisation.

 

Table 72. Normalisation relationships between soil CEC and the toxicity of nickel (Ni) to a variety of soil plant and invertebrate species and soil microbial processes for both fresh and aged contamination. The relationships used to normalise the toxicity data in this project are in bold.

Eqn no.

Species/soil process

Y parameter

X parameter(s)

Reference

Northern hemisphere relationshipsa

1

Glucose induced respiration

log EC50 (fresh)

0.95 log CEC + 1.51 (r2 = 0.82)

Oorts et al. 2006b

2

log EC50 (aged)

1.34 log CEC + 1.38 (r2 = 0.92)

Oorts et al. 2006b

3

Maize residue mineralisation

log EC20 (fresh)

0.86 log CEC + 1.48 (r2 = 0.55)

Oorts et al. 2006b

4

log EC20 (aged)

1.22 log CEC + 1.37 (r2 = 0.72)

Oorts et al. 2006b

5

Nitrification

log EC50 (fresh)

0.79 log CEC + 1.44 (r2 = 0.69)

Oorts et al. 2006b

6

log EC50 (aged)

1.00 log CEC + 1.42 (r2 = 0.60)

Oorts et al. 2006b

7

Barley root elongation

log EC50 (fresh)

0.90 log CEC + 1.60 (r2 = 0.92)

Rooney et al. 2007

8

log EC50 (aged)

1.12 log CEC + 1.57 (r2 = 0.83)

Rooney et al. 2007

9

Tomato shoot yield

log EC50 (fresh)

1.06 log CEC + 1.09 (r2 = 0.77)

Rooney et al. 2007

10

log EC50 (aged)

1.27 log CEC + 1.06 (r2 = 0.67)

Rooney et al. 2007

11

F. candida (collembola)

log EC50 (fresh)

0.97 log CEC + 1.71 (r2 = 0.84)

EC 2008b

12

log EC50 (aged)

1.17 log CEC + 1.70 (r2 = 0.71)

EC 2008b

13

Eisenia. fetida (earthworm)

log EC50 (fresh)

0.72 log CEC + 1.79 (r2 = 0.74)

EC 2008b

14

log EC50 (aged)

0.95 log CEC + 1.76 (r2 = 0.72)

EC 2008b

a = all the CEC measurements were made using the silver thiourea method (Chhabra et al. 1975).

 

Table 73. The normalisation relationships for nickel (Ni) that could explain more than 50% of the variation in the NOEC and 10% effect concentration (EC10) data. The x and y parameters in each equation are the logarithms of the CEC and of the NOEC or EC10 toxicity data, respectively. The relationships used to normalise the toxicity data in this project are in bold.

Eqn no.

Species and end point

X parameter(s)a

1

Tomato (shoot yield)

1.068 x + 0.908 (r2 = 0.76)

2

Barley (root elongation)

0.87 x + 1.35 (r2 = 0.86)

3

All invertebrates (mixed endpoints)

0.78 x + 1.51 (r2 = 0.56)

4

Glucose respiration

1.42 x – 0.38 (r2 = 0.58)

5

Maize residue mineralisation

0.67 x + 1.45 (r2 = 0.53)

6

Respiration

2.37 x – 0.36 (r2 = 0.92)

a = all CEC measurements were made using the silver thiourea method (Chhabra et al. 1975).

Figure 9 shows the SSD (that is, the cumulative distribution of the geometric means of normalised NOEC and EC10 toxicity values) for the species used to derive the Ni SQGs. While there is an abundance of terrestrial toxicity data for Ni, the majority of data is for microbial processes and microbial enzymes, with only small amounts of data for plants and invertebrates. There does not appear to be any difference in the sensitivity of microbial processes and both plants and invertebrates. However, the distributions of the sensitivities of the plants and invertebrates only just overlap. Nonetheless, there are no marked differences in the sensitivity of the three groups of organisms and therefore all the available toxicity data was used to derive the Ni SQGs.

 

Figure 9. The SSD of normalised NOEC and 10% effect concentration (EC10) toxicity data for fresh nickel (Ni) contamination against soil Ni concentration for soil invertebrates, plants and microbial processes.

 

Soil quality guidelines were derived using three different sets of toxicity data (that is, NOEC and EC10, LOEC and EC30, and EC50 data) as part of this study.

All the toxicity data was normalised as set out earlier. The generic ACL(NOEC & EC10) values generated for fresh Ni contamination for the three land uses are presented in Table 74.

Table 74. Generic ACLS for fresh nickel (Ni) contamination based on NOEC and 10% effect concentration (EC10) toxicity data for various land uses.

Land use

Generic added contaminant limit
(mg added/kg)

Areas of ecological significance

6

Residential urban/public open space

50

Commercial/industrial

95

The normalisation equations were then used to calculate soil-specific ACL values at a range of CEC values. Then the lowest ACL at each CEC value was adopted as the soil-specific ACL (Table 75).

Table 75. The soil-specific ACLs (mg/kg) at a range of cation exchange capacities for fresh nickel (Ni) contamination based on NOEC and 10% effect concentration (EC10) toxicity data.

Land use

Cation exchange capacities (cmolc/kg)a

5

10

20

30

40

60

Areas of ecological significance

1

6

9

10

15

20

Residential urban/public open space

10

50

80

110

130

170

Commercial/industrial

20

95

150

200

240

310

a = all CEC measurements were made using the silver thiourea method (Chhabra et al. 1975).

For sites with no history of Ni contamination, the method of Hamon et al. (2004) is recommended in Schedule B5b to estimate the ABC. The equation to predict the ABC for Ni is

 

log Ni conc (mg/kg) = 0.702 log Fe content (%) + 0.834              (equation 10)

 

Examples of the ABC values predicted by this equation are presented in Table 76.

 


Table 76. ABCs for nickel (Ni) predicted using the equation from method of Hamon et al. (2004) (equation 10 above).

Fe content (%)

Predicted ABC
(mg/kg)

0.1

1

0.5

4

1

7

2

10

5

20

10

35

15

45

20

55

Predicted ABC values for Ni range from approximately 1 to 55 mg/kg in soils with iron contents between 0.1 and 20%.

To calculate the Ni SQG(NOEC & EC10) values, the ABC value is added to the ACL(NOEC & EC10). ABC values vary with soil type. Therefore, it is not possible to present a single set of SQG(NOEC & EC10) values. Thus, two examples of Ni SQG(NOEC & EC10) values for urban contaminated soils are provided below. These examples would be at the low and high end of the range of SQG values (but not the extreme values) generated for Australian soils.

 

Example 1

Site descriptors urban residential land/public open space use in a new suburb (that is, fresh contamination).

Soil descriptors a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   50 mg/kg

ABC:     7 mg/kg

SQG(NOEC & EC10):   57 mg/kg, which would be rounded off to 55 mg/kg.

 

Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(NOEC & EC10)ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   240 mg/kg

ABC:    35 mg/kg

SQG(NOEC & EC10):   275 mg/kg, which would be rounded off to 270 mg/kg.

 

To maximise the data available to generate the ACL(LOEC & EC30) and ACL(EC50), the available toxicity data was converted to the appropriate measure of toxicity using the conversion factors recommended in Schedule B5b and presented in Table 17. As there were normalisation equations available, soil-specific ACLs could be generated. The ACL(LOEC & EC30) and ACL(EC50) values were calculated using the same method as that for the corresponding values for Cu and Pb and are presented in Table 77.

Table 77. The soil-specific ACLs (mg/kg) at a range of cation exchange capacities for fresh nickel (Ni) contamination based on LOEC and 30% effect concentration (EC30) toxicity data, and based on 50% effect concentration (EC50) toxicity data.

Land use

Cation exchange capacities (cmolc/kg)

5

10

20

30

40

60

 

Based on LOEC and EC30 data

Areas of ecological significance

1

7

10

15

15

25

Residential urban/public open space

10

50

85

110

130

170

Commercial/industrial

20

100

170

220

260

350

 

Based on EC50 data

Areas of ecological significance

5

25

40

55

65

90

Residential urban/public open space

30

160

250

330

400

520

Commercial/industrial

55

280

450

590

710

940

The ABC values for Ni were calculated using the method previously set out, and the values presented in Table 76.

To calculate the Ni SQG(LOEC & EC30) and the SQG(EC50) values, the ABC value is added to the corresponding ACL values. ABC values and Ni ACL values vary with soil type. Therefore it is not possible to present a single set of SQG(LOEC & EC30) or SQG(EC50) values. Thus, two examples of Ni SQG(LOEC & EC30) and two examples for Ni SQG(EC50) are provided below. These examples would be at the low and high end of the range of SQG values (but not the extreme values) generated for Australian soils.


SQG(LOEC & EC30) Example 1

Site descriptors urban residential land/public open space use in a new suburb (that is, fresh contamination).

Soil descriptors a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    50 mg/kg

ABC:     7 mg/kg

SQG(LOEC & EC30):    57 mg/kg, which would be rounded off to 55 mg/kg.

 

SQG(LOEC & EC30) Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    260 mg/kg

ABC:    35 mg/kg

SQG(LOEC & EC30):    295 mg/kg, which would be rounded off to 290 mg/kg.

 

SQG(EC50) Example 1

Site descriptors urban residential land/public open space use in a new suburb (that is, fresh contamination).

Soil descriptors a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    160 mg/kg

ABC:     7 mg/kg

SQG(EC50):    167 mg/kg, which would be rounded off to 170 mg/kg

 

SQG(EC50) Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    710 mg/kg

ABC:    35 mg/kg

SQG(EC50):    745 mg/kg, which would be rounded off to 750 mg/kg.

 


Smolders et al. (2009) state that, based on an extensive review of the literature, the ALF for Ni is a function of soil pH (measured in 0.01 M calcium chloride solution) and ranges between 1 and 3.5. Further detail on this relationship is provided in the EU ecological risk assessment report for Ni (EC 2008b). The relationship between the ALF and soil pH is:

ALF = 1 + exp(1.4(soil pH 7.0)              (equation 11)

However, using this equation indicates that the ALF will rapidly increase after a soil pH of 7.5 to values considerably higher than 3.5 (Table 78).

Table 78. ALF values for nickel (Ni) at various soil pH values. The ALF values were derived using the relationship from the European Union ecological risk assessment for Ni (EC 2008b).

Soil pH (CaCl2)

ALF

5

1.07

6

1.25

7

2.00

7.5

3.01

8

5.06

8.5

9.17

9.0

17.45

The above ALF values were calculated after a maximum of 1.5 years ageing in the field, therefore in most ‘aged’ Australian sites the ALFs would be larger. However, there is no information available that would permit estimates of how much larger the ALFs would be and therefore the above ALF values were used to calculate the Ni SQGs.

There are two possible approaches to incorporating the relationship between ALF and soil pH into the methodology for deriving SQGs. In the first, a soil pH that is reasonably representative or protective of the majority of Australian soils is selected and the corresponding ALF is then used to calculate the aged SQGs. The resulting SQGs would be protective of all aged soils with a pH higher than the selected pH, but would not provide the same level of protection to soils with lower soil pH. Such soils would have to proceed to further desktop analysis by using the ALFpH relationship to determine the appropriate ALF for that soil and then apply that to the fresh contamination SQGs. To maximise the utility of this approach and minimise the number of sites that would require the additional analysis, the selected soil pH would have to be low, perhaps as low as 5. This would result in an ALF of 1.07 and with such a small increase in the resulting aged SQGs, it is doubtful that it would be of any real benefit.

 

The second approach would be to fully adopt the ALFpH relationship into the methodology for deriving SQGs, where the pH of the site would need to be determined and then the appropriate ALF calculated for the site and applied to the toxicity data to generate the aged contamination ACLs and thence the aged SQGs. While the latter is more complex, the benefits of having the most scientifically defensible ACLs and SQGs outweigh this. It is recommended that SQGs are derived by multiplying fresh (non-aged and non-leached) toxicity data by the ALF determined using the ALFpH relationship (see equation 11).

The aged SQG(NOEC & EC10) values for Ni were calculated using the same methodology as that used for the SQG(NOEC & EC10) values for fresh Ni contamination, with two exceptions. These were (i) that the ‘fresh’ toxicity data was corrected using the Ni ALFs (equation 11) and (ii) the ABCs were the 25th percentile values for old suburbs from Olszowy et al. (1995). The resulting ACL(NOEC & EC10) values for aged Ni contamination are presented in Table 79.

Table 79. The soil-specific ACLs (mg/kg) at a range of cation exchange capacities for aged nickel (Ni) contamination based on NOEC and 10% effect concentration (EC10) toxicity data.

Land use

Cation exchange capacities (cmolc/kg)

5

10

20

30

40

60

Areas of ecological significance

2

9

15

20

20

30

Residential urban/public open space

15

85

140

180

220

290

Commercial/industrial

30

160

250

330

400

530

 

For aged contaminated sites (that is, the contamination has been in place for at least 2 years) Heemsbergen et al. (2008) recommends using the 25th percentiles of the ABC data for ‘old suburbs’ in Olszowy et al. (1995) (see Table 80). The Olszowy et al. (1995) data is derived from soils low in geogenic Ni and, by using low ABCs, could create low SQGs in some areas with naturally high background Ni concentrations. This problem could be overcome in areas with elevated soil Ni by using measured ABC values or using the method of Hamon et al. (2004).

Table 80. Nickel (Ni) ABCs based on the 25 percentiles of Ni concentrations in ‘old suburbs’ (i.e. >2 years old) from various states of Australia (Olszowy et al. 1995).

Suburb type

25th percentile of Ni ABC values (mg/kg)

NSW

QLD

SA

VIC

Old suburb, low traffic

5

5

6

5

Old suburb, high traffic

5

4

6

10

 

To calculate the aged Ni SQG(NOEC & EC10) values , the ABC value is added to the ACL. Ambient background concentration values vary with soil type, region and history of exposure to contamination. Therefore, it is not possible to present a single set of SQG(NOEC & EC10) values. Thus, two examples of Ni SQG(NOEC & EC10) values are presented below. These examples would be at the low and high end of the range of SQG values (but not the extreme values) generated for Australian soils.

Example 1

Site descriptors urban residential land/public open space use in an old Queensland suburb (that is, aged contamination), with low traffic volume.

Soil descriptors a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   85 mg/kg

ABC:     5 mg/kg

SQG(NOEC & EC10):   90 mg/kg

 

Example 2

Site descriptors commercial/industrial land use in an old Victorian suburb (that is, aged contamination), with high traffic volume.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   400 mg/kg

ABC:    10 mg/kg

SQG(NOEC & EC10):   410 mg/kg

Soil-specific aged Ni ACL values based on LOEC and EC30 and on EC50 data were calculated using the method previously set out, except the type of toxicity data used was different. The resulting ACLs are presented in Table 81.

Table 81. The soil-specific ACLs at a range of cation exchange capacities for aged nickel (Ni) contamination based on lowest observed effect concentration (LOEC) and 30% effect concentration (EC30) toxicity data, and based on 50% effect concentration (EC50) toxicity data.

Land use

Cation exchange capacities (cmolc/kg)

5

10

20

30

40

60

 

Based on LOEC and EC30 data

Areas of ecological significance

5

30

45

60

70

95

Urban residential/public open space

30

170

270

350

420

560

Commercial/industrial

55

290

460

600

730

960

 

Based on EC50 data

Areas of ecological significance

10

65

100

130

160

210

Urban residential/public open space

55

270

440

570

700

910

Commercial/industrial

90

460

730

960

1200

1500

 

The ABC values used for aged Ni were obtained from Table 80.

Ambient background concentration values for Ni vary with soil type as do the Ni ACL values. Therefore, it is not possible to present a single set of SQG(LOEC & EC30) or SQG(EC50) values. Thus, two examples of Ni SQG(LOEC & EC30) values and two examples for Ni SQG(EC50) values are provided below. These examples would be at the low and high end of the range of SQG values (but not the extreme values) generated for Australian soils.

 

SQG(LOEC & EC30) Example 1

Site descriptors urban residential land/public open space use in an old Queensland suburb (that is, aged contamination), with high traffic volume.

Soil descriptors a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    170 mg/kg

ABC:     4 mg/kg

SQG(LOEC & EC30):    174 mg/kg, which would be rounded off to 170 mg/kg.

 

SQG(LOEC & EC30) Example 2

Site descriptors commercial/industrial land use in an old Victorian suburb, with high traffic volume.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    730 mg/kg

ABC:    10 mg/kg

SQG(LOEC & EC30):    740 mg/kg

 

SQG(EC50) Example 1

Site descriptors urban residential land/public open space use in an old Queensland suburb (that is, aged contamination), with high traffic volume.

Soil descriptors a sandy acidic soil (pH 5, CEC 10) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    270 mg/kg

ABC:     4 mg/kg

SQG(EC50):    274 mg/kg, which would be rounded off to 270 mg/kg.

 

SQG(EC50) Example 2

Site descriptors commercial/industrial land use in an old Victorian suburb, with high traffic volume.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40) with 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    1200 mg/kg

ABC:    10 mg/kg

SQG(EC50):    1210 mg/kg, which would be rounded off to 1200 mg/kg.

 

The SQGs for Ni were considered to be of high reliability, as the toxicity data set met the minimum data requirements to use an SSD method and there were normalisation relationships available to account for soil characteristics (Schedule B5b).

Soil quality guidelines for Ni in a number of international jurisdictions are presented in Table 82. These SQGs have a variety of purposes and levels of protection and therefore a comparison of the values is problematic. The SQGs for Ni range from 24 to 500 mg/kg added and total Ni, with both of these values coming from countries within the EU. The superseded interim urban EIL for Ni (NEPC 1999) was 60 mg/kg total Ni.

 

There are also four health-based investigation level (HIL) values that range from 400 to 4000 mg/kg total Ni (see Schedule B1). The urban residential/public open space ACLs based on NOEC and EC10, LOEC and EC30, and EC50 data for fresh Ni contamination range from 10170, 10–170, and 30 to 520 mg/kg added Ni respectively. These correspond to the minimal risk, warning risk and the potential risk values of EU member countries and the values are very similar. The urban residential/public open space ACLs based on NOEC and EC10, LOEC and EC30, and EC50 data for aged Ni contamination range from 15290, 30560, and 55910 mg/kg added Ni respectively. These limits permit higher concentrations than in any of the other jurisdictions, but this is not suprising as the other jurisdictions do not account for ageing or leaching, nor do they take into account the bioavailability in different soils.

 

The most meaningful comparisons can be made between the SQGs and the concentrations that would protect 95% of species based on NOEC and EC10 data that was derived in the EU ecological risk assessment for Ni (EC 2008b). These values ranged from 8.3 to 188.7 mg/kg added Ni for soils with CEC values ranging from 2.4 to 36 cmolc/kg (EC 2008b). SQGs that protected 95% of species were not derived, but rather the SQGs were derived that protect 99, 80 and 60% of species. The SQGs that aim to protect 99% of species based on NOEC and EC10 data ranged from 120 mg/kg added Ni. The SQGs that aim to protect 80% of species based on NOEC and EC10 data ranged from 10170mg/kg added Ni. These comparisons indicate that the SQGs derived in this project are slightly more conservative than the EU values, but overall the values are similar.

 

Table 82. Soil quality guidelines for nickel (Ni) in a number of international jurisdictions.

Name of the Ni soil quality guideline

Value of the guideline

(mg/kg Ni)

Dutch target values1 

35 (added Ni)

Dutch intervention value1

210 (added Ni)

Canadian SQG (residential, commercial and industrial)2

50 (total Ni)

Eco-SSL plants3

38 (total Ni)

Eco-SSL soil invertebrates3

280 (total Ni)

Eco-SSL avian3

210 (total Ni)

Eco-SSL mammalian3

130 (total Ni)

EU minimal risk values (residential)4

2460 (added & total Ni)

EU warning risk values (residential)

30180 (added & total Ni)

EU potential risk values (residential)4

30500 (added & total Ni)

EU Ni ecological risk assessment (conc that should protect 95% of species)5

8.3188.7 (added & total Ni)

1 = VROM 2000

2 = CCME 1999g 2006 and http://ceqg-rcqe.ccme.ca/

3 = http://www.epa.gov/ecotox/ecossl/

4 = Carlon 2007

5 = EC 2008b.

 

10             Trivalent chromium

Chromium occurs in a number of oxidation states: II, III, IV, V and VI. The two dominant states in soils are trivalent (III) and hexavalent (VI) Cr. The only forms of Cr (III) for which there was toxicity data were chromium chloride, chromium nitrate and chromium sulphate.

Chromium is the seventh most abundant element (McGrath & Smith 1990). It is also an essential element for humans and for some groups of organisms (Crommentuijn et al. 2000), yet the hexavalent form is generally considered to be highly toxic and a carcinogen.

 

The two key considerations in determining the most important exposure pathways for inorganic contaminants, such as Cr (III), are whether they biomagnify and whether they have the potential to leach to groundwater. A surrogate measure of the potential for a contaminant to leach is its watersoil partition coefficient (Kd). If the logarithm of the Kd (log Kd) of an inorganic contaminant is less than 3 then it is considered to have the potential to leach to groundwater (Schedule B5b). The log Kd reported by Commentuijn et al. (2000) for Cr (with the oxidation state not identified) was 2.04 L/kg; therefore, Cr has the potential in some soils to leach to groundwater. However, the ability of Cr to migrate from soil to either groundwater or surface water depends greatly on its oxidation state. Hexavalent Cr is highly water-soluble whereas trivalent Cr is almost insoluble in water and immobile in soil (Bartlett & James 1988; Cervantes et al. 2001). Therefore, Cr (III) is unlikely to pose an environmental risk by leaching. In addition, Cr (III) cannot cross most cells (Cervantes et al. 2001). In contrast, Cr (VI) is actively transported across cell membranes (Dreyfuss, 1964; Wiegand et al. 1985). Chromium (III) is not known to biomagnify (Scott-Fordsmand & Pedersen 1995; Heemsbergen et al. [2008]) and therefore only direct toxicity routes of exposure were considered in deriving the SQGs for Cr (III).

Unlike the preceding elements, there is a lack of ecotoxicity data for Cr (III). This is reflected by the fact that the US EPA (US EPA 2008) could not derive Eco-SSL values (which require toxicity data for species belonging to three different types of organisms) for Cr (either as III or VI) for soil invertebrates and plants. Also, neither the Canadians (CCME 1999h,) nor the Dutch (Crommentuijn et al. 2000) have SQGs for Cr (III) but simply total Cr.

 

Extensive searches of the available scientific literature were conducted on ISI web of knowledge, the US EPA ECOTOX database (http://cfpub.epa.gov/ecotox), the Dutch RIVM e-toxbase database (http://www.e-toxbase.com – this is not publicly available), the database of the French National Institute of Industrial Environment and Risk (INERIS, www.ineris.fr), and the Australasian Ecotoxicology Database (Warne et al. 1998; Warne & Westbury 1999; Markich et al. 2002; Langdon et al. 2009). There were a number of publications (Bonet et al. 1991; Scoccianti et al. 2006) which presented toxicity data for Cr (III) that were not included in the derivation of SQGs in this guideline. This was because these were based on exposing plants solely via aqueous media (that is, hydroponics) or the growth medium was agar and this is vastly different from exposure via soil.

 

The raw toxicity data for Cr (III) is presented in Appendix I. The toxicity data (geometric means for each species) used to calculate the SQGs is presented in Table 83. There was toxicity data for a total of 21 species or soil microbial processes. There was data for 2 soil invertebrate species, 12 species of plants and 7 soil microbial processes. This data meets the minimum data requirements recommended in Schedule B5b to use the BurrliOZ SSD method (Campbell et al. 2000). The toxicity data for nitrogenase was not used as it was all less than values and the lowest concentration tested (that is, 50 mg/kg) caused an effect considerably larger than 50%. It should be noted that the toxicity data for the enzyme catalase was markedly lower (that is, more than one order of magnitude) than all the other toxicity data. Given this and the fact that the toxicity data was quantified using nominal (not measured) concentrations, there is uncertainty in the reliability of this data. Therefore the catalase toxicity data was not used to derive the SQGs.

Table 83. The lowest geometric mean values of normalised (invertebrate) and non-normalised (all other species and microbial processes) trivalent chromium (Cr (III)) toxicity data, expressed in terms of added Cr (III) for soil invertebrate species, plant species, and soil microbial processes.

Test species

Geometric mean (mg/kg)

Common name

Scientific name

EC10 or NOEC

EC30 or LOEC

EC50

Arylsulfatase

 

121

181

321

Barley

H. vulgare

200

300

600

Beans

 

200

500

600

Bent grass

Agrostis tenius

3333

5000

10000

Bush bean

Phaseolus vulgaris

41

70.7

141

Catalase

 

0.19

0.88

2.32

Corn

Z. mays

294

611

1233

Earthworm

Eisenia fetida

467

700

1400

Earthworm

E. Andrei

25.4

79.5

159

Glutamic acid decomposition

 

55

400

800

Grass

 

200

500

600

Indian mustard

Brassica juncea

500

750

1100

Lettuce

L. sativa

500

387

775

Nitrogenase

 

<<50

<<50

<<50

Nitrogen mineralisation

 

172

302

626

Nitrogenate formation

 

50

200

500

Oat

A. sativa

339

508

1016

Perennial ryegrass

L. perenne

3333

5000

10000

Radish

R. sativus

500

387

775

Respiration

 

36.3

114

139

Rye

Secale cereale

233

350

700

Urease

 

71.2

122

205

 

In order to maximise the use of the available toxicity data, conversion factors provided in Schedule B5b were used to permit the inter-conversion of NOEC, LOEC, EC50, EC30 and EC10 data. The conversion factors used are presented in Table 17.

There are only three published normalisation relationships for Cr (III) toxicity (Sivakumar & Subbhuraam 2005). They all relate the toxicity of Cr (III) to survival of E. fetida and are presented in Table 84. These are all based on clay content. The logarithmic form of normalisation relationship 1 was used to normalise the E. fetida and E. andrei toxicity data. This relationship was not applied to the toxicity data of the other species/microbial processes as they do not belong to the same organism type (that is, soft-bodied invertebrate) as the earthworm. This approach is consistent with the method recommended in Schedule B5b and adopted in the various EU ecological risk assessments that have been conducted for metals (EC 2008a; EC 2008b; LDA 2008).

Table 84. Normalisation relationships for the toxicity of trivalent chromium (Cr (III)) to soil invertebrates. The relationship used to normalise the toxicity data is in bold. All equations from Sivakumar & Subbhuraam (2005).

Species/soil process

Y Parameter

X parameter(s)

E. fetida

log EC50

-5.46 clay content + 1905.93
(r2 = 0.92)

-5.75 clay content – 10.62 pH + 1980.46 (r2 = 0.92)

-3.59 clay content + 4.16 pH + 65.83 soil N + 1748.22 (r2 = 0.95)

 

Figure 10 shows the SSD (that is, the cumulative distribution of the geometric means of species sensitivities to Cr (III)) for all species for which Cr (III) toxicity data was available). Due to the limited amount of Cr (III) toxicity data and the fact that the data was not normalised (and thus soil properties affect the values), it is difficult to draw conclusions regarding the relative sensitivity of plants, invertebrates and soil processes to Cr (III). Given the lack of data and the overlaps in the sensitivity of the organism types, all the Cr (III) toxicity data was used to derive the SQGs.

Figure 10. The SSD (plotted as a cumulative frequency against added trivalent chromium (Cr (III)) concentration) of Cr (III) for soil invertebrate species, plant species and soil microbial processes.

 

Only the Cr (III) toxicity data for E. fetida and E. andrei could be normalised to the Australian reference soil. Thus, a set of generic ACLs and a set of soil-specific ACLs were derived (for the earthworms). The soil-specific ACL values below a clay content of 10% were smaller than the generic ACL values. The soil-specific ACL at a clay content of 10% equalled the generic ACL, and all soil-specific ACLs for soils with a clay content greater than 10% were larger than the generic ACLs. The lower of the soil-specific ACL values and the generic ACL values were adopted as the final ACLs for Cr (III). Thus, the situation was simplified to the soil-specific ACLs only applying up to a clay content of 10% at which point the generic ACL values apply. The generated ACLs for the three land uses and the three types of toxicity data (that is, NOEC and EC10, LOEC and EC30, EC50) are presented in Table 85.

 

The range between the largest and smallest ACL values generated was approximately 4.0 to 470 mg added Cr (III)/kg. The residential/urban ACLs based on NOEC and EC10, LOEC and EC30, and EC50 data ranged from 3575, 75160, and 110230 mg added Cr (III)/kg respectively.

 

Table 85. The ACLs based on NOEC and 10% effect concentration (EC10) data, LOEC and 30% effect concentration (EC30), and 50% effect concentration (EC50) toxicity data for trivalent chromium (Cr (III)) for various land uses. These are based on all the Cr (III) toxicity data, except the catalase and nitrogenase enzyme activity data.

Data type

Land use

Clay content

1

2.5

5

≥10

NOEC

AES

4

6

7

9

 

UR

35

45

60

75

 

C/I

65

90

110

140

LOEC

AES

25

30

40

50

 

UR

75

100

130

160

 

C/I

120

170

210

270

EC50

AES

9

10

15

20

 

UR

110

150

190

230

 

C/I

220

300

375

470

AES = Areas of ecological significance

UR = urban residential/public open space

C/I = commercial/industrial land uses.

For sites with no history of Cr (III) contamination, the method of Hamon et al. (2004) is recommended to estimate the Cr ABC. Technically this method predicts total Cr but under aerobic soil conditions the vast majority of Cr will be present as Cr (III). It is therefore appropriate to use the Hamon et al (2004) method to estimate Cr (III) ABC values. The equation to predict the Cr ABC is:

 

log Cr conc (mg/kg) = 0.75 log Fe content (%) + 1.242            (equation 12)

 

Examples of the ABC values predicted by this equation are presented in Table 86. Predicted ABC values for Cr (III) range from approximately 3 to 160 mg/kg in soils with iron concentrations between 0.1 and 20%.

 

Table 86. ABCs for chromium (Cr) predicted using the method of Hamon et al. (2004) (equation 12 above).

Fe content (%)

Predicted Cr ABC (mg/kg)

0.1

3

0.5

10

1

15

2

30

5

60

10

100

15

130

20

160

 

ABC values for Cr (III) vary with soil type (Table 86). Therefore, it is not possible to present a single set of SQG values. Thus, two examples of each of Cr (III) SQG(NOEC & EC10) values, SQG(LOEC & EC30) values and SQG(EC50) values are provided below. These examples would be at the low and high end of the range of SQG values (but not the extreme values) generated for Australian soils.

SQG(NOEC & EC10) Example 1

Site descriptors urban residential land/public open space use in a new suburb.

Soil descriptors a sandy acidic soil (pH 5, CEC 10, clay content 2.5%) with 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   45 mg/kg

ABC:     15 mg/kg

SQG(NOEC & EC10):   60 mg/kg

 

SQG(NOEC & EC10) Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40, clay content 20%) with 10% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   140 mg/kg

ABC:    100 mg/kg

SQG(NOEC & EC10):   240 mg/kg

 


 

SQG(LOEC & EC30) Example 1

Site descriptors urban residential land /public open space use in a new suburb.

Soil descriptors a sandy acidic soil (pH 5, CEC 10, clay content 2.5%) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    100 mg/kg

ABC:     15 mg/kg

SQG(LOEC & EC30):    115 mg/kg, which would be rounded off to 110 mg/kg.

 

SQG(LOEC & EC30) Example 2

Site descriptors commercial/industrial land use/public open space in a new suburb.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40, clay content 20%) with 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    270 mg/kg

ABC:    100 mg/kg

SQG(LOEC & EC30):    370 mg/kg

 

SQG(EC50) Example 1

Site descriptors urban residential land/public open space use in a new suburb.

Soil descriptors a sandy acidic soil (pH 5, CEC 10, clay content 2.5%) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    150 mg/kg

ABC:     15 mg/kg

SQG(EC50):    165 mg/kg, which would be rounded off to 160 mg/kg.

 

SQG(EC50) Example 2

Site descriptors commercial/industrial land use in a new suburb.

Soil descriptors an alkaline clay soil (clay content 20%) with 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    470 mg/kg

ABC:    100 mg/kg

SQG(EC50):    570 mg/kg

 

There are no ALFs available for Cr (III) nor data available to derive ALFs. Therefore, as an interim measure, the mean of the ALF values available for other cations (that is, Cd, Cu, Co, Ni, Pb and Zn) from Smolders et al. (2009) was determined. This resulted in a value of 2.35[4], which was rounded off to 2.5.

All the Cr (III) toxicity data was multiplied by the ALF of 2.5. Therefore, the aged SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values are exactly 2.5 times the corresponding fresh SQGs for Cr (III). The resulting aged SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values are presented in Table 87.

For aged contaminated sites (that is, the contamination has been in place for at least 2 years, Schedule B5b) the methodology recommends using the 25th percentiles of the ABC data for the ‘old suburbs’ of Olszowy et al. (1995) (see Table 88). Chromium concentrations in old suburbs are higher than those for new suburbs (Olszowy et al. 1995); therefore, it is appropriate to use the ABC values for aged suburbs. The Cr concentrations reported by Olszowy et al (1995) are for total Cr; however, as was the case with the Hamon et al. (2004) method, the majority of the Cr measured will be Cr (III) and thus the data can be used to estimate ABC values for Cr (III). The Olszowy et al. (1995) data was derived from soils low in geogenic Cr and, by using low ABCs, could create low SQGs in some areas with naturally high background Cr concentrations. This problem could be overcome in areas of high natural Cr (III) by using measured ABC values or using the Hamon et al. (2004) method.

Table 87. The ACLs based on NOEC and 10% effect concentration (EC10) data, LOEC and 30% effect concentration (EC30), and 50% effect concentration (EC50) toxicity data for trivalent chromium (Cr (III)) for various land uses. These are based on all the Cr (III) toxicity data, except the catalase and nitrogenase enzyme activity data.

Data type

Land use

Clay content

1

2.5

5

≥10

NOEC

AES

10

15

20

20

 

UR

85

120

150

190

 

C/I

170

230

280

360

LOEC

AES

60

80

100

130

 

UR

190

250

310

400

 

C/I

310

420

530

660

EC50

AES

25

30

40

50

 

UR

275

370

460

580

 

C/I

550

750

940

1200

AES = Areas of ecological significance, UR = urban residential/public open space, C/I = commercial/industrial land uses.

 

Table 88. Chromium ABCs based on the 25th percentiles of Cr concentrations in ‘old suburbs’ (that is, >2 years old) from various states of Australia (Olszowy et al. 1995).

Suburb type

25th percentile of Cr ABC values (mg/kg)

NSW

QLD

SA

VIC

Old suburb, low traffic

8

15

15

10

Old suburb, high traffic

15

7

15

10

 

ABC values for Cr (III) vary with soil type and location (Table 88). Therefore, it is not possible to present a single set of SQG values. Thus, two examples of each of Cr (III) SQG(NOEC & EC10) values, SQG(LOEC & EC30) values and SQG(EC50) values for aged Cr (III) contamination are provided below. These examples would be at the low and high end of the range of SQG values (but not the extreme values) generated for Australian soils.

 

SQG(NOEC & EC10) Example 1

Site descriptors urban residential land /public open space use in an old Victorian suburb with low traffic volume.

Soil descriptors a sandy acidic soil (pH 5, CEC 10, clay content 2.5%) with 1% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   120 mg/kg

ABC:     10 mg/kg

SQG(NOEC & EC10):   130 mg/kg

 

SQG(NOEC & EC10) Example 2

Site descriptors commercial/industrial land use in an old NSW suburb with high traffic volume.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40, clay content 20%) with 10% iron content.

The resulting ACL(NOEC & EC10), ABC and SQG(NOEC & EC10) values are:

ACL(NOEC & EC10):   360 mg/kg

ABC:    15 mg/kg

SQG(NOEC & EC10):   375 mg/kg, which would be rounded off to 370 mg/kg.

 

SQG(LOEC & EC30) Example 1

Site descriptors urban residential land/public open space use in an old Victorian suburb with low traffic volume.

Soil descriptors a sandy acidic soil (pH 5, CEC 10, clay content 2.5%) with 1% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    250 mg/kg

ABC:     10 mg/kg

SQG(LOEC & EC30):    260 mg/kg

 

SQG(LOEC & EC30) Example 2

Site descriptors commercial/industrial land use in an old NSW suburb with high traffic volume.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40, clay content 20%) with 10% iron content.

The resulting ACL(LOEC & EC30), ABC and SQG(LOEC & EC30) values are:

ACL(LOEC & EC30):    660 mg/kg

ABC:    15 mg/kg

SQG(LOEC & EC30):    675 mg/kg, which would be rounded off to 670 mg/kg.

 

SQG(EC50) Example 1

Site descriptors urban residential land/public open space use in an old Victorian suburb with low traffic volume.

Soil descriptors a sandy acidic soil (pH 5, CEC 10, clay content 2.5%) with 1% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    370 mg/kg

ABC:     10 mg/kg

SQG(EC50):    380 mg/kg

 

SQG(EC50) Example 2

Site descriptors commercial/industrial land use in an old NSW suburb with high traffic volume.

Soil descriptors an alkaline clay soil (pH 7.5, CEC 40, clay content 20%) with 10% iron content.

The resulting ACL(EC50), ABC and SQG(EC50) values are:

ACL(EC50):    1200 mg/kg

ABC:    15 mg/kg

SQG(EC50):    1215 mg/kg, which would be rounded off to 1200 mg/kg.

 

The Cr (III) toxicity data set met the minimum data requirements to use the SSD method but there was only one normalisation relationship available (for the earthworm Eisenia fetida) to account for soil characteristics. Based on the criteria for assessing the reliability of SQGs in Schedule B5b, this means that the Cr (III) SQGs were considered to be of moderate reliability.

 

A compilation of SQGs for Cr (III), Cr (VI) and total Cr from a number of international jurisdictions is presented in Table 89. These guidelines have a variety of purposes and levels of protection and therefore comparison of the values is problematic. The SQGs for Cr (III) range from 2650 mg/kg (total Cr (III)). The majority of jurisdictions do not have SQGs for Cr (III), more typically they have SQGs for total Cr. Carlon (2007), in his review of the SQGs of members of the EU, did not identify whether the SQGs were for added or total Cr, nonetheless they range from 341000 mg/kg. Hexavalent Cr is typically considered to be more toxic than Cr (III) and this is reflected by it having lower SQGs (Table 89).

 

The  ACLs for fresh Cr (III) contamination that apply to urban residential land/public open space land use based on NOEC and EC10, LOEC and EC30, and EC50 data ranged from 3575, 75160 and 100230 mg added Cr (III)/kg respectively. The SQGs based on NOEC and EC10 data are closest to the existing international SQGs for Cr (III). It should be noted that all of the  ACLs for urban residential land/public open space land use (irrespective of what data was used to generate them) are considerably smaller than the superseded interim urban EIL of 400 mg total Cr/kg (NEPC 1999). However, the ACLs are consistent with the available Cr (III) toxicity data where there are 6 species/microbial processes that have EC50 values below the superseded interim urban EIL and there are 12 and 16 species/microbial processes that have LOEC and EC30 or NOEC and EC10 data respectively, below the superseded interim urban EIL. The species/microbial processes with toxicity values below the superseded interim urban EIL can be indentified by referring to Table 83.

 

The  ACLs for aged Cr (III) contamination that apply to urban residential land/public open space land use based on NOEC and EC10, LOEC and EC30, and EC50 data ranged from 85190, 175400 and 270580 mg added Cr (III)/kg respectively. None of the ACLs based on NOEC & EC10 and LOEC & EC30 toxicity data were larger than the current interim EIL. However, once the clay content was 5% or above, the ACL values based on EC50 data were larger than the superseded interim EIL. All of the ACLs for aged Cr (III) contamination are considerably larger than the collated international Cr (III) SQGs.

 

Table 89. Soil quality guidelines (mg/kg) for total chromium, trivalent chromium (Cr (III)) and hexavalent chromium (Cr (VI)) from international jurisdictions.

 

Name of chromium soil quality guideline

Total chromium

Trivalent chromium

Hexavalent chromium

Canadian SQG (residential)1

 

 

0.4 (total)

Canadian SQG (commercial and industrial)1

 

 

1.4 (total)

Danish soil quality guideline2

 

50 (total)

2 (total)

Dutch target value3

100 (added Cr)

 

 

Dutch maximum permissible addition3

380 (added Cr)

 

 

Eco-SSL plants4

 

ID

ID

Eco-SSL soil invertebrates4

 

ID

ID

Eco-SSL avian4

 

26 (total)

ID

Eco-SSL mammalian4

 

34 (total)

130 (total)

EU minimal risk values (residential)5

34130 (added & total)

 

2.5 (added & total)

EU warning risk values (residential)5

50450 (added & total)

 

4.220 (added & total)

EU potential risk values (residential)5

1001000 (added & total)

 

 

1 = CCME 1999h and 2006 and http://ceqg-rcqe.ccme.ca/

2 = Scott-Fordsmand and Pedersen 1995

3 = VROM 2000

4 =  http://www.epa.gov/ecotox/ecossl/

5 = Carlon 2007

ID = insufficient data.

11             Summary

The methodology for deriving SQGs, detailed in Schedule B5b, was implemented to calculate SQGs based on different types of toxicity data for eight contaminants (arsenic, chromium, copper, DDT, lead, naphthalene, nickel, zinc). These eight chemicals were selected as they have a variety of physicochemical properties and, as a result, would behave differently in the environment. They are frequently found in urban Australian contaminated sites. The results of this process are summarised below for each contaminant. Some contaminants have the potential to leach from the contaminated site and thus may cause deleterious effects on groundwater and surface water ecosystems. The fact that contaminants can leach can be taken into account in deriving SQGs. This was done for zinc and arsenic, to illustrate the process and to illustrate the effect that it can have on the resulting SQG.

 

There was a considerable amount of toxicity data available for the essential element zinc. Zinc does not biomagnify but has the potential to leach from contaminated soil to groundwater. The minimum data requirements to use the SSD method were exceeded, there were multiple normalisation relationships, and there was an ageing/leaching factor. The toxicity data could be expressed in terms of added Zn concentrations; therefore, high reliability soil-specific Zn ACL(NOEC & EC10), ACL(LOEC & EC30) and ACL(EC50) values and corresponding SQG values could be derived for:

Soil-specific ACLs could be derived, so a suite of values were generated. For example, the ACL(NOEC & EC10) values for urban residential/public open space sites freshly contaminated with Zn ranged from 20 (at a cation exchange capacity of 5 and a soil pH of 4) to 330 mg/kg (at a cation exchange capacity of 60 and a soil pH of 7.5). The range of ACL values reflects the ability of different soils to modify the bioavailability and toxicity of Zn. Correcting for ageing led to a marked increase in the ACL values. The corresponding ACL(NOEC & EC10) values for aged Zn contamination range from 45800 mg/kg. As such, correcting for the ageing of Zn led to a more than doubling of the recommended ACL values. The ACL(LOEC & EC30) and ACL(EC50) values were approximately 1.252 and 1.52 times larger, respectively, than the corresponding ACL(NOEC & EC10) values. The lowest of the Zn ACLs for urban residential land/public open space (20 mg/kg) are essentially identical to the lowest corresponding international SQGs, while the higher Zn ACLs are considerably larger than any international SQG.

 

Arsenic does not biomagnify in oxidised soils but has the potential to leach from contaminated soil to groundwater. Therefore, only the direct toxicity route of exposure needs to be considered in deriving the SQGs. The minimum data requirements to use the SSD method were exceeded, there were no normalisation relationships, and an ageing/leaching factor was available.

 

The toxicity data could only be expressed in terms of total As concentrations, therefore moderate reliability generic (not soil-specific) As SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values could be derived for:

 

The generic As SQG(NOEC & EC10) value for soils with areas of ecological significance, urban residential/public open space and commercial/industrial land uses were 8, 20 and 30 mg/kg (total As) respectively. The SQG(LOEC & EC30) and SQG(EC50) values were approximately 2.55 and 3.755 times larger, respectively, than the corresponding SQG(NOEC & EC10) values. The As SQG(NOEC & EC10) for urban residential/public open space soils is identical to the superseded interim urban EIL of 20 mg/kg (NEPC1999). Both the As SQG(NOEC & EC10) and the superseded EIL lie in the lower portion of the range of international As SQGs. The SQG(NOEC & EC10) for aged contamination, at 40 mg/kg, was twice the superseded interim urban EIL for As. The aged As SQG(LOEC & EC30) for urban residential/public open space soils lies in the upper part of the range of international SQGs while the aged As SQG(EC50) value for urban residential/public open space soils is markedly larger than any other international SQG.

 

Naphthalene does not biomagnify and has only a moderate potential to leach to groundwater. Therefore, only the direct toxicity exposure route was considered in deriving the SQGs. The minimum data requirements to use the SSD method were exceeded, there were no normalisation relationships, and there was no ageing/leaching factor. The toxicity data could only be expressed as total naphthalene concentrations. Therefore, moderate reliability generic (not soil-specific) naphthalene SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) values could be derived for:

The generic naphthalene SQG(NOEC & EC10) values for soils with areas of ecological significance, urban residential/public open space and commercial/industrial land uses were 5, 70 and 150 mg/kg (total naphthalene) respectively. The SQG(LOEC & EC30) and SQG(EC50) values were approximately 22.5 and 5 times larger, respectively, than the corresponding SQG(NOEC & EC10) values. There is only a very limited number of international SQGs for naphthalene, which differ markedly (that is, from 0.6 to 125). The SQG(NOEC & EC10) for urban residential/public open space soils of 70 mg/kg is very similar to the top of the EU range of SQGs and in the middle of the range of collated international SQGs.

 

DDT biomagnifies and has a very low potential to leach to groundwater. Therefore, only the biomagnification and direct toxicity exposure pathways were assessed in deriving SQGs. The minimum data requirements to use the SSD method were exceeded, there were no normalisation relationships, and there was no ageing/leaching factor. The toxicity data could only be expressed as total DDT concentrations. Therefore, moderate reliability generic (not soil-specific) DDT SQG(NOEC & EC10), SQG(LOEC & EC30) and SQG(EC50) could be derived for:

The generic DDT SQG(NOEC & EC10) values for soils with areas of ecological significance, urban residential/public open space and commercial/industrial land uses were 1, 70 and 250 mg/kg (total DDT) respectively. The SQG(LOEC & EC30) and SQG(EC50) values were approximately 2.6 2 and 56 times larger, respectively, than the corresponding SQG(NOEC & EC10) values. The international SQGs for DDT range from 0.01 to 4 mg/kg. The  SQG(NOEC & EC10) value for freshly contaminated urban residential/public open space soil is thus considerably larger than the international guidelines but is considerably smaller than the HILs, which range from 260 to 4000 mg/kg (see Schedule B1).

 

Copper is an essential element. It has a low potential to leach to groundwater. Copper does not biomagnify and therefore only direct toxic effects were considered. There was an extensive toxicity data set for Cu (39 species or soil microbial processes). There were normalisation relationships available for plants, invertebrates and soil microbial processes. An ageing/leaching factor was also available. Therefore high reliability soil-specific ACLs could be derived using NOEC and EC10, LOEC and EC30, and EC50 data for:

The ACL(NOEC and EC10) values for urban residential/public open space sites freshly contaminated with Cu ranged from approximately 20 (at a soil pH of 4.5) to 70 mg added Cu/kg (at a soil pH of 8). Correcting for ageing led to a marked increase in the ACL values. The corresponding ACL values for aged Cu contamination range from 30120 mg added Cu/kg. The range of ACL values reflects the ability of different soils to modify the bioavailability and toxicity of Cu. The ACLs based on LOEC and EC30 data and based on EC50 data were approximately 1.52 and 2.53 times larger, respectively, than the corresponding SQGs based on NOEC and EC10 data. All of the Cu ACLs for residential land use lie within the range of international SQGs for Cu (141000 mg/kg). The superseded interim urban EIL for Cu was 100 mg/kg (total Cu). Therefore the superseded interim EIL for Cu falls within the range of values of all of the SQGs for urban residential land/public open space land uses. The SQGs will permit both considerably less and considerably more Cu in urban residential/public open space soils, depending on the properties of the soils.

 

Lead is not an essential element but it does not biomagnify in terrestrial ecosystems, nor does it have any significant potential to leach to groundwater. There was toxicity data for 19 species and soil microbial processes which included plants, invertebrates and soil microbial processes. There were no useful normalisation relationships. An ageing/leaching factor has been published in the literature. Therefore moderate reliability generic (not soil-specific) Pb SQGs could be derived using NOEC and EC10, LOEC and EC30, and EC50 data for:

The generic Pb ACL for urban residential/public open space land use that was calculated using NOEC and EC10 data was 130 mg added Pb/kg. The equivalent SQG for aged Pb contamination was 530 mg added Pb/kg. The corresponding ACLs calculated using LOEC and EC30 and using EC50 data were approximately 2 and 4 times larger than the NOEC and EC10 derived ACL values. All the Pb ACLs for urban residential/public open space soils fell within the range of SQGs that have been adopted in other international jurisdictions (25700 mg/kg).

 

The superseded interim urban EIL was 600 mg/kg (total Pb). All of the Pb SQGs for fresh contamination are lower than the superseded interim urban EIL. The aged SQGs based on NOEC and EC10 are slightly smaller than the superseded interim urban EIL, while the SQGs based on LOEC and EC30 and based on EC50 data are considerably higher.

 

Nickel does not biomagnify so only the direct toxicity exposure route was considered in deriving the SQGs. Nickel, however, does have the potential to leach to groundwater. There was toxicity data for a total of 53 plant and animal species or soil microbial processes. In addition, there were normalisation relationships available for invertebrates, plants and soil microbial processes. A soil pH-modified ageing/leaching factor was available. The minimum data requirements to use the SSD method were exceeded, there were no normalisation relationships, and there was no ageing/leaching factor. Therefore high reliability soil-specific ACLs could be derived using NOEC and EC10, LOEC and EC30, and EC50 data for:

The soil-specific Ni ACLs based on NOEC and EC10 data for urban residential/public open space soils ranged from 10170 mg added Ni/kg for soils with a CEC ranging from 5 to 60 cmolc/kg. The corresponding ACL values for aged Ni contamination ranged from 15290 mg added Ni/kg. The ACL values based on LOEC and EC30 data and based on EC50 data were essentially identical and approximately 3 times larger than the NOEC and EC10-based ACL values. The range of international SQGs for Ni is 24500 mg/kg. Thus, only the urban residential/public open space ACLs for soils with a CEC above 40 cmolc/kg lie outside the range of internationally adopted SQGs. The superseded interim urban EIL for Ni was 60 mg/kg (total Ni). All of the SQGs would permit both lower and higher concentrations than the superseded interim urban EIL. In soils with a low Ni bioavailability, the maximum recommended concentration of Ni that can be added is 15 times the superseded interim urban EIL.

 

Trivalent chromium is an essential element for humans and animals but not for plants. It does not pose a potential environmental problem due to leaching (unless it is oxidised to hexavalent chromium), nor does it biomagnify. Toxicity data was available for a total of 21 invertebrate and plant species and soil microbial processes. There were only normalisation relationships available for earthworms. There was no ageing/leaching factor available for Cr (III). Therefore moderate reliability soil-specific ACLs could be derived using NOEC and EC10, LOEC and EC30, and EC50 data for:

The  soil-specific Cr (III) ACL values based on NOEC and EC10 data for urban residential/ public open space land uses ranged from 3575 mg added Cr (III)/kg for soils with a clay content from 1 to greater than 10%. The ACL values based on LOEC and EC30 and based on EC50 data were approximately 2 and 3 times larger than the NOEC-based ACLs. The ACLs for aged Cr (III) contamination were approximately 2.5 times larger than the corresponding ACLs for fresh contamination. The ACLs for Cr (III) based on NOEC and EC10 data are consistent with other internationally adopted Cr (III) SQGs. The ACL values based on LOEC and EC30 and on EC50 data are larger than the current international Cr (III) SQGs.

 

The superseded interim urban EIL for total Cr was 400 mg/kg. This is considerably higher than any of the SQGs for fresh Cr (III) by a factor of at least 2.6. The aged ACLs are essentially 2.5 times larger than the corresponding fresh ACLs.

 

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13             Appendices

There are three tables in this appendix (Tables A1 to A3).

Table A1: Raw toxicity data for zinc to soil microbial processes with the corresponding toxicity values when they were normalised to the Australian reference soil, the corresponding values when corrected for ageing and leaching, and the source of the data.

Geographical location

Soil process

Soil pH

Delta pH

EC10 or NOEC

Log EC10 or NOEC

Log normalised EC10 or NOEC

Normalised EC10 or NOEC

Age corrected normalised EC10 or NOEC

Source

Europe

Acetate decomposition

7.4

-1.4

303

2.48

2.27

187

560

Vanbeelen et al. 1994

Europe

Amidase

7.4

-1.4

200

2.3

2.09

123

370

Hemida et al. 1997

Europe

Amidase

7.5

-1.5

200

2.3

2.08

119

357

Hemida et al. 1997

Europe

Ammonification

7.1

-1.1

1000

3

2.84

684

2052

Premi & Cornfield 1969

Europe

Arylsulphatase

6.2

-0.2

820

2.91

2.88

765

2296

Al-Khafaji & Tabatabai 1979

Europe

Arylsulphatase

7.8

-1.8

140

2.15

1.88

75

226

Al-Khafaji & Tabatabai 1979

Europe

Arylsulphatase

5.8

0.2

164

2.21

2.24

176

527

Al-Khafaji & Tabatabai 1979

Europe

Arylsulphatase

7.4

-1.4

820

2.91

2.7

506

1517

Al-Khafaji & Tabatabai 1979

Europe

Arylsulphatase

5.1

0.9

728

2.86

3

993

2980

Haanstra & Doelman 1991

Europe

Arylsulphatase

7.7

-1.7

105

2.02

1.77

58.4

175

Haanstra & Doelman 1991

Europe

Arylsulphatase

6.8

-0.8

2353

3.37

3.25

1785

5355

Haanstra & Doelman 1991

Europe

Arylsulphatase

7.4

-1.4

151

2.18

1.97

93

279

Haanstra & Doelman 1991

Europe

Denitrification

6.8

-0.8

100

2

1.88

76

228

Bollag & Barabasz 1979

Europe

Nitrate reductase

7.4

-1.4

67

1.83

1.62

41

124

Hemida et al. 1997

Europe

N-mineralisation

6.9

-0.9

100

2

1.87

73

220

Chang & Broadbent 1982

Europe

N-mineralisation

5.8

0.2

164

2.21

2.24

176

527

Liang & Tabatabai 1977

Europe

N-mineralisation

6.6

-0.6

164

2.21

2.12

133

400

Liang & Tabatabai 1977

Europe

N-mineralisation

7.8

-1.8

164

2.21

1.94

88

264

Liang & Tabatabai 1977

Europe

N-mineralisation

7.4

-1.4

164

2.21

2

101

303

Liang & Tabatabai 1977

Europe

N-mineralisation

3.4

2.6

233

2.37

2.76

572

1716

Necker & Kunze 1986

Europe

Phosphatase

5.1

0.9

1341

3.13

3.26

1830

5490

Doelman & Haanstra 1989

Europe

Phosphatase

6.8

-0.8

160

2.2

2.08

121

364

Doelman & Haanstra 1989

Europe

Phosphatase

7.4

-1.4

2623

3.42

3.21

1617

4852

Doelman & Haanstra 1989

Europe

Phosphatase

5.8

0.2

164

2.21

2.24

176

527

Juma & Tabatabai 1977

Europe

Phosphatase

7.4

-1.4

164

2.21

2

101

303

Juma & Tabatabai 1977

Europe

Phosphatase

4.7

1.3

508

2.71

2.9

796

2388

Svenson 1986

Europe

Phytase

4.7

1.3

590

2.77

2.97

924

2773

Svenson 1986

Europe

Py-phosphatase

4.6

1.4

1640

3.21

3.42

2660

7979

Stott et al. 1985

Europe

Py-phosphatase

6.2

-0.2

1640

3.21

3.18

1531

4592

Stott et al. 1985

Europe

Py-phosphatase

7.4

-1.4

1640

3.21

3

1011

3034

Stott et al. 1985

Europe

Respiration

6.9

-0.9

17

1.23

1.1

12

37

Chang & Broadbent 1981

Europe

Respiration

6.7

-0.7

110

2.04

1.94

86

259

Lighthart et al. 1983

Europe

Respiration

7

-1

165

2.22

2.07

117

350

Lighthart et al. 1983

Europe

Respiration

7.2

-1.2

110

2.04

1.86

73

218

Lighthart et al. 1983

Europe

Respiration

8.2

-2.2

17

1.23

0.9

8

24

Lighthart et al. 1983

Europe

Respiration

5.2

0.8

50

1.7

1.82

66

198

Saviozzi et al. 1997

Europe

Respiration

3

3

120

2.08

2.53

338

1015

Smolders et al, 2003

Europe

Respiration

4.8

1.2

469

2.67

2.85

710

2130

Smolders et al, 2003

Europe

Respiration

5.1

0.9

50

1.7

1.83

68

205

Smolders et al. 2003

Europe

Respiration

5.7

0.3

1400

3.15

3.19

1553

4659

Smolders et al. 2003

Europe

Respiration

6.8

-0.8

38

1.58

1.46

29

86

Smolders et al. 2003

Europe

Respiration

7.4

-1.4

150

2.18

1.97

92

277

Smolders et al. 2003

Europe

Respiration

7.4

-1.4

600

2.78

2.57

370

1110

Smolders et al. 2003

Europe

Respiration

7.5

-1.5

150

2.18

1.95

89

268

Smolders et al. 2003

Europe

Respiration

7.5

-1.5

300

2.48

2.25

179

536

Smolders et al. 2003

Australia

SIN1

5.42

0.58

209

2.32

2.52

328

328

NBRP unpublished data2

Australia

SIN

4.52

1.48

63

1.8

2.3

200

200

NBRP unpublished data

Australia

SIN

7.26

-1.26

1181

3.07

2.64

440

440

NBRP unpublished data

Australia

SIN

4.89

1.12

346

2.54

2.92

829

829

NBRP unpublished data

Australia

SIN

3.96

2.04

10

1.01

1.7

50

50

NBRP unpublished data

Australia

SIN

4.39

1.61

70

1.84

2.39

247

247

NBRP unpublished data

Australia

SIN

5.03

0.97

270

2.43

2.76

577

577

NBRP unpublished data

Australia

SIN

5.13

0.87

901

2.95

3.25

1782

1782

NBRP unpublished data

Australia

SIN

6.32

-0.32

919

2.96

2.85

716

716

NBRP unpublished data

Australia

SIN

6.33

-0.33

462

2.66

2.55

357

356

NBRP unpublished data

Australia

SIN

4.8

1.2

188

2.27

2.68

482

482

NBRP unpublished data

Australia

SIN

7.63

-1.63

7538

3.88

3.32

2110

2110

NBRP unpublished data

Australia

SIR3

5.42

0.58

158

2.2

2.4

249

249

NBRP unpublished data

Australia

SIR

4.52

1.48

369

2.57

3.07

1176

1176

NBRP unpublished data

Australia

SIR

7.26

-1.26

187

2.27

1.84

70

70

NBRP unpublished data

Australia

SIR

4.89

1.12

462

2.66

3.04

1105

1105

NBRP unpublished data

Australia

SIR

4.39

1.61

73

1.86

2.41

257

257

NBRP unpublished data

Australia

SIR

5.03

0.97

499

2.7

3.03

1064

1064

NBRP unpublished data

Australia

SIR

5.13

0.87

281

2.45

2.74

555

555

NBRP unpublished data

Australia

SIR

6.32

-0.32

25

1.41

1.3

20

20

NBRP unpublished data

Australia

SIR

6.33

-0.33

268

2.43

2.32

207

207

NBRP unpublished data

Australia

SIR

4.8

1.2

345

2.54

2.95

885

885

NBRP unpublished data

Australia

SIR

7.63

-1.63

190

2.28

1.73

53

53

NBRP unpublished data

Europe

Urease

5.1

0.9

30

1.48

1.61

41

123

Doelman & Haanstra 1986

Europe

Urease

7.7

-1.7

70

1.85

1.59

39

117

Doelman & Haanstra 1986

Europe

Urease

6.8

-0.8

460

2.66

2.54

349

1047

Doelman & Haanstra 1986

Europe

Urease

7.4

-1.4

30

1.48

1.27

19

55

Doelman & Haanstra 1986

Europe

Urease

7.4

-1.4

64

1.81

1.6

39

118

Tabatabai 1977

Europe

Urease

7.8

-1.8

52

1.72

1.45

28

84

Tabatabai 1977

Europe

Urease

5.8

0.2

109

2.04

2.07

117

350

Tabatabai 1977

1 SIN = substrate induced nitrification

2 = This EC10 data has not been published but was determined using the same biological response and soil concentration data as the EC50 values published in Broos et al. (2007)

3 SIR = substrate induced respiration.


Table A2: Raw toxicity data for zinc to soil invertebrates with the corresponding toxicity values when they were normalised to the Australian reference soil, the corresponding values when corrected for ageing and leaching, and the source of the data.

1 CEC = cation exchange capacity 2 A. = Aporrectodea 3 C. = Caenorhabditis 4. dauer larval stage 5 E. = Eisenia 6 E. = Enchytraeus 7 F. = Folsomia 8 L. = Lumbriculus.


Table A3: Raw toxicity data for zinc to plant species with the corresponding toxicity values when they were normalised to the Australian reference soil, the corresponding values when corrected for ageing and leaching, and the source of the data. The wheat toxicity was sourced from Warne et al. (2008a), all other Australian data is unpublished data from the Australian National Biosolids Research Program.

Scientific name

Toxicity end point

CEC1

Log CEC

Delta log CEC

EC10 or NOEC

Log EC10 or NOEC

Log normalised EC10

Normalised EC10

Aged normalised EC10

Source

Acrobeloides sp.

 

3.6

0.56

0.44

99

1.99

2.34

221

663

Korthals et al. 1996

A. rosea2

survival

15

1.18

-0.18

538

2.73

2.59

391

1172

Spurgeon & Hopkin 1996

A. caliginosa

reproduction

9.2

0.97

0.03

210

2.32

2.35

223

669

Spurgeon et al. 2000

C. elegans3

 

2.4

0.38

0.62

112

2.05

2.54

345

1035

Boyd & Williams 2003

C. elegans

 

7.2

0.86

0.14

118

2.07

2.18

153

458

Boyd & Williams 2003

C. elegans

 

28.4

1.45

-0.45

383

2.58

2.22

168

504

Boyd & Williams 2003

C. elegans

 

10.0

1

0

25

1.4

1.4

25

76

Jonker et al. 2004

C. elegans4

 

3.6

0.56

0.44

308

2.49

2.84

689

2068

Korthals et al. 1996

E. andrei5

reproduction

26

1.41

-0.41

320

2.51

2.18

152

456

van Gestel et al. 1993

E. fetida5

reproduction

26

1.41

-0.41

350

2.54

2.22

166

499

Spurgeon et al. 1997

E. fetida

reproduction

26

1.41

-0.41

350

2.54

2.22

166

499

Spurgeon et al. 1997

E. fetida

reproduction

15

1.18

-0.18

237

2.37

2.24

172

516

Spurgeon & Hopkin 1996

E. fetida

reproduction

15

1.18

-0.18

199

2.3

2.16

144

433

Spurgeon et al. 1994

E. fetida

reproduction

26

1.41

-0.41

553

2.74

2.42

263

788

Spurgeon & Hopkin 1996

E. fetida

reproduction

18

1.27

-0.27

97

1.99

1.78

60

179

Spurgeon & Hopkin 1996

E. fetida

reproduction

33

1.52

-0.52

484

2.68

2.28

189

568

Spurgeon & Hopkin 1996

E. fetida

reproduction

16

1.21

-0.21

85

1.93

1.77

58

175

Spurgeon & Hopkin 1996

E. fetida

reproduction

22

1.34

-0.34

183

2.26

2

99

297

Spurgeon & Hopkin 1996

E. fetida

reproduction

27

1.44

-0.44

414

2.62

2.27

186

559

Spurgeon & Hopkin 1996

E. fetida

reproduction

14

1.14

-0.14

115

2.06

1.95

90

269

Spurgeon & Hopkin 1996

E. fetida

reproduction

18

1.25

-0.25

161

2.21

2.01

101

304

Spurgeon & Hopkin 1996

E. fetida

reproduction

22

1.35

-0.35

223

2.35

2.08

119

357

Spurgeon & Hopkin 1996

E. fetida

reproduction

5.8

0.76

0.24

180

2.26

2.44

277

830

Smolders et al. 2003

E. fetida

reproduction

1.9

0.28

0.72

100

2

2.57

371

1114

Smolders et al. 2003

E. fetida

reproduction

13.3

1.12

-0.12

320

2.51

2.41

255

766

Smolders et al. 2003

E. fetida

reproduction

11.2

1.05

-0.05

560

2.75

2.71

512

1536

Smolders et al. 2003

E. fetida

reproduction

4.7

0.67

0.33

320

2.51

2.76

581

1743

Smolders et al. 2003

E. fetida

reproduction

21.1

1.32

-0.32

1000

3

2.74

554

1663

Smolders et al. 2003

E. fetida

reproduction

23.4

1.37

-0.37

560

2.75

2.46

286

858

Smolders et al. 2003

E. fetida

reproduction

8.9

0.95

0.05

180

2.26

2.3

197

592

Smolders et al. 2003

E. fetida

reproduction

20.1

1.3

-0.3

180

2.26

2.02

104

311

Smolders et al. 2003

E. fetida

reproduction

16.9

1.23

-0.23

350

2.54

2.36

231

694

Smolders et al. 2003

E. fetida

reproduction

15

1.18

-0.18

572

2.76

2.62

415

1246

Spurgeon & Hopkin 1996

E. fetida

reproduction

9.2

0.97

0.03

792

2.9

2.93

843

2530

Spurgeon et al. 2000

E. albidus6

 

15

1.18

-0.18

262

2.42

2.28

190

571

Lock & Janssen 2001

E. albidus

 

15

1.18

-0.18

132

2.12

1.98

96

287

Lock & Janssen 2001

E. albidus

 

15

1.18

-0.18

180

2.26

2.12

131

392

Lock & Janssen 2001

E. albidus

 

11.5

1.06

-0.06

100

2

1.95

90

269

Lock & Janssen 2001

E. crypticus6

 

15

1.18

-0.18

380

2.58

2.44

276

828

Lock & Janssen 2001

Eucephalobus sp.

 

3.6

0.56

0.44

60

1.78

2.13

134

403

Korthals et al. 1996

F. candida7

reproduction

26

1.41

-0.41

366

2.56

2.1

125

375

Smit & van Gestel 1998

F. candida

reproduction

26

1.41

-0.41

620

2.79

2.33

212

636

Sandifer & Hopkin 1996

F. candida

reproduction

26

1.41

-0.41

399

2.6

2.13

136

409

van Gestel & Hensbergen 1997

F. candida

reproduction

5

0.66

0.34

275

2.44

2.83

680

2040

Smit & van Gestel 1998

F. candida

reproduction

5

0.66

0.34

314

2.5

2.89

776

2329

Smit & van Gestel 1998

F. candida

reproduction

22

1.34

-0.34

300

2.48

2.09

123

370

Sandifer & Hopkin 1996

F. candida

reproduction

20

1.3

-0.3

300

2.48

2.14

137

411

Sandifer & Hopkin 1996

F. candida

reproduction

26

1.41

-0.41

300

2.48

2.01

103

308

Sandifer & Hopkin 1997

F. candida

reproduction

1.9

0.28

0.72

32

1.51

2.33

213

638

Smolders et al. 2003

F. candida

reproduction

13.3

1.12

-0.12

320

2.51

2.36

231

694

Smolders et al. 2003

F. candida

reproduction

11.2

1.05

-0.05

100

2

1.94

88

264

Smolders et al, 2003

F. candida

reproduction

22.6

1.35

-0.35

320

2.51

2.1

126

379

Smolders et al. 2003

F. candida

reproduction

21.1

1.32

-0.32

320

2.51

2.14

137

410

Smolders et al. 2003

F. candida

reproduction

20

1.3

-0.3

560

2.75

2.41

254

762

Smolders et al. 2003

F. candida

reproduction

36.3

1.56

-0.56

1000

3

2.36

230

690

Smolders et al. 2003

F. candida

reproduction

16.9

1.23

-0.23

320

2.51

2.25

176

528

Smolders et al. 2003

L. rubellus8

reproduction

15

1.18

-0.18

121

2.08

1.94

88

264

Spurgeon & Hopkin 1996

L. rubellus

reproduction

9.2

0.97

0.03

517

2.71

2.74

550

1649

Spurgeon et al. 2000

L. rubellus

reproduction

9.2

0.97

0.03

325

2.51

2.54

346

1039

Spurgeon & Hopkin 1999

L. rubellus

reproduction

9.2

0.97

0.03

648

2.81

2.84

690

2069

Spurgeon & Hopkin 1999

L. rubellus

reproduction

9.2

0.97

0.03

470

2.67

2.7

500

1501

Spurgeon & Hopkin 1999

L. terrestris8

reproduction

9.2

0.97

0.03

998

3

3.03

1062

3187

Spurgeon et al. 2000

Nematode community

 

5.1

0.7

0.3

560

2.75

2.98

961

2882

Smit et al. 2002

Nematode community

 

5.1

0.7

0.3

180

2.26

2.49

309

926

Smit et al. 2002

Nematode community

 

5.1

0.7

0.3

180

2.26

2.49

309

926

Smit et al. 2002

Nematode community

 

5.1

0.7

0.3

56

1.75

1.98

96

288

Smit et al. 2002

Plectus sp.

 

3.6

0.56

0.44

10

1.02

1.37

23

70

Korthals et al. 1996

Rhabditidae sp.

 

3.6

0.56

0.44

89

1.95

2.3

199

597

Korthals et al. 1996

Site

Plant species

Scientific name

CEC

Log CEC

Delta CEC

pH

Delta pH

EC10

Log EC10

Log normalised EC10

Normalised EC10

Aged normalised EC10

Europe1

Alfalfa

Medicago sativa

 

 

7.50

-1.50

300.00

2.48

2.30

198.21

594.62

Australia

Barley

Hordeum vulgare

9.95

1.00

0.00

7.63

-1.63

56.36

1.75

1.31

20.49

20.49

Australia

Barley

H. vulgare

17.71

1.25

-0.25

6.32

-0.32

490.45

2.69

2.43

268.91

268.91

Australia

Barley

H. vulgare

10.29

1.01

-0.01

6.33

-0.33

486.69

2.69

2.59

387.88

387.88

Europe1

Barley

H. vulgare

 

 

7.50

-1.50

100.00

2.00

1.82

 

 

Europe2

Barley

H. vulgare

17.64

1.25

-0.25

5.60

0.40

33.30

1.52

1.35

22.44

67.31

Europe3

Barley

H. vulgare

 

 

7.80

-1.80

215.00

2.33

2.12

 

 

Europe1

Beet

Beta vulgaris

 

 

7.50

-1.50

300.00

2.48

2.30

198.21

594.62

Europe4

Black or white lentil

Vigna mungo L.

 

 

6.20

-0.20

100.00

2.00

1.98

94.62

283.87

Australia

Canola

Brassica napus

10.29

1.01

-0.01

6.33

-0.33

178.84

2.25

2.15

142.53

142.53

Australia

Canola

B. napus

3.16

0.50

0.50

5.42

0.58

139.13

2.14

2.65

448.08

448.08

Australia

Canola

B. napus

4.95

0.69

0.31

4.80

1.20

52.26

1.72

2.26

181.45

181.45

Australia

Canola

B. napus

12.99

1.11

-0.11

4.89

1.12

144.60

2.16

2.38

241.34

241.34

Europe5

Common vetch

Vicia sativa

12.46

1.10

 

5.00

1.00

32.00

1.51

1.63

42.18

126.55

Australia

Cotton

Gossypium sp

60.97

1.79

-0.79

7.26

-1.26

2127.60

3.33

2.44

272.44

272.44

Europe6

Fenugreek

Trigonella foenum graceum

17.02

1.23

 

8.30

-2.30

200.00

2.30

2.03

105.93

317.80

Europe1

Lettuce

Lactuca sativa

 

 

7.50

-1.50

400.00

2.60

2.42

264.28

792.83

Australia

Maize

Zea mays

16.51

1.22

-0.22

5.03

0.97

500.53

2.70

2.81

644.29

644.29

Europe7

Maize

Z. mays

11.58

1.06

-0.06

4.90

1.10

83.00

1.92

1.99

98.72

296.17

Europe1

Maize

Z. mays

 

 

7.50

-1.50

300.00

2.48

2.30

198.21

594.62

Europe1

Maize

Z. mays

 

 

7.50

-1.50

200.00

2.30

2.12

132.14

396.42

Australia

Millet

Panicum milaceum

16.51

1.22

-0.22

5.03

0.97

419.12

2.62

2.73

539.50

539.50

Europe8

Oats

Avena sativa

9.19

0.96

0.04

5.60

0.40

100.00

2.00

2.08

120.38

361.14

Europe8

Oats

A. sativa

24.02

1.38

-0.38

5.40

0.60

200.00

2.30

2.03

108.22

324.66

Europe8

Oats

A. sativa

5.50

0.74

0.26

5.00

1.00

200.00

2.30

2.65

448.99

1346.96

Europe8

Oats

A. sativa

11.50

1.06

-0.06

5.40

0.60

400.00

2.60

2.62

417.04

1251.11

Europe6

Onion

Allium cepa

17.02

1.23

-0.23

8.30

-2.30

200.00

2.30

1.82

65.97

197.92

Europe1

Pea

Pisum sativum (perfection)

 

7.50

-1.50

400.00

2.60

2.42

264.28

792.83

Australia

Peanuts

Arachis hypogaea

16.51

1.22

-0.22

5.03

0.97

227.06

2.36

2.47

292.27

292.27

Australia

Peanuts

A. hypogaea

4.94

0.69

0.31

4.52

1.48

16.29

1.21

1.83

67.27

67.27

Europe5

Red clover

Trifolium pratense

26.42

1.42

 

6.20

-6.20

100.00

2.00

1.26

18.03

54.09

Europe5

Red clover

T. pratense

26.42

1.42

 

6.20

-0.20

84.00

1.92

1.90

79.48

238.45

Europe5

Red clover

T. pratense

12.46

1.10

 

5.00

1.00

32.00

1.51

1.63

42.18

126.55

Europe5

Red clover

T. pratense

3.52

0.55

 

5.30

0.70

32.00

1.51

1.59

38.83

116.49

Europe9

Red clover

T. pratense

3.52

0.55

 

5.30

0.70

32.00

1.51

1.59

38.83

116.49

Europe9

Red clover

T. pratense

3.52

0.55

 

5.30

0.70

32.00

1.51

1.59

38.83

116.49

Europe1

Spinach

Spinacia oleracea

 

 

7.50

-1.50

200.00

2.30

2.12

132.14

396.42

Australia

Sorghum

Sorghum spp

60.97

1.79

-0.79

7.26

-1.26

1660.64

3.22

2.33

212.64

212.64

Europe1

Sorghum

S. bicolor var RS-626)

 

7.50

-1.50

200.00

2.30

2.12

132.14

396.42

Europe1

Sorghum

S. bicolor var XK-125)

 

7.50

-1.50

100.00

2.00

1.82

66.07

198.21

Australia

Sugar cane

Saccharum

4.94

0.69

0.31

4.52

1.48

780.00

2.89

3.51

3220.34

3220.34

Europe1

Tomato

Lycopersicon esculentum

 

7.50

-1.50

400.00

2.60

2.42

264.28

792.83

Australia

Triticale

Tritosecale

11.58

1.06

-0.06

3.96

2.04

310.18

2.49

3.00

998.11

998.11

Australia

Wheat

Triticum aestivum

9.95

1.00

0.00

7.63

-1.63

4764.45

3.68

3.24

1732.26

1732.26

Australia

Wheat

T. aestivum

3.16

0.50

0.50

5.42

0.58

91.05

1.96

2.47

293.23

293.23

Australia

Wheat

T. aestivum

7.82

0.89

0.11

4.39

1.61

373.62

2.57

3.08

1215.42

1215.42

Australia

Wheat

T. aestivum

17.71

1.25

-0.25

6.32

-0.32

1216.50

3.09

2.82

667.01

667.01

Australia

Wheat

T. aestivum

17.41

1.24

-0.24

5.13

0.87

1312.80

3.12

3.19

1532.36

1532.36

Australia

Wheat

T. aestivum

10.29

1.01

-0.01

6.33

-0.33

688.94

2.84

2.74

549.07

549.07

Australia

Wheat

T. aestivum

4.95

0.69

0.31

4.80

1.20

101.93

2.01

2.55

353.88

353.88

Australia

Wheat

T. aestivum

16.51

1.22

-0.22

5.03

0.97

262.46

2.42

2.53

337.84

337.84

Australia

Wheat

T. aestivum

60.97

1.79

-0.79

7.26

-1.26

2351.09

3.37

2.48

301.05

301.05

Australia

Wheat

T. aestivum

12.99

1.11

-0.11

4.89

1.12

428.96

2.63

2.85

715.97

715.97

Australia

Wheat

T. aestivum

11.58

1.06

-0.06

3.96

2.04

255.16

2.41

2.91

821.05

821.05

1 Boawn and Rasmussen 1971; 2 Luo and Rimmer 1995; 3 Aery and Jagatiya 1997; 4 Kalyanaraman and Sivagurunathan 1993; 5 van der Hoeven & Henzen 1994; 6 Dang et al. 1990; 7 MacLean 1974; 8 De Haan et al. 1985;  9 Hooftman and Henzen 1996.

There are two tables in this appendix (Tables B1 and B2).

Table B1:  Raw toxicity data for arsenic to plants with the corresponding toxicity values when they were converted to NOEC values.

Crop

Toxic concentration soil (mg/kg)

Reported toxic effect (%)

Interpreted toxic effect

Est. NOEC

(mg/kg)

Source

 

Range

Value or mean of range

Barley

 

283

lower yield

LOEC

113.2

Cooper et al. 1931

Barley

 

 

90

NOEC

 

Davis et al. 1978

Bean

010

5

5895

LOEC

2.07

Woolson 1973

Bean

<25

 

86

NOEC

 

Stewart & Smith 1922

Bean

 

25

lower yield

LOEC

10

Walsh & Keeney 1975

Bean

 

25

lower yield

LOEC

10

Sandberg & Allen 1975

Bean

045

22.5

89

NOEC

22.5

Jacobs and Keeney 1970

Bean

 

140

77 (NS)

NOEC

140

Chisholm & MacPhee 1972

Bean

 

140

40

EC50

28

MacPhee et al. 1960

Bean

 

414

71

LOEC

414

Clements & Munson 1947

Blueberry

 

44

lower yield

LOEC

17.6

Walsh & Keeney 1975

Blueberry

 

70

78

LOEC

70

Anastasia & Kender 1973

Corn

10100

55

55

EC50

11

Woolson et al. 1971

Corn

 

20

70

LOEC

8

Jacobs & Keeney 1970

Corn

 

20

90

NOEC

20

Jacobs & Keeney 1970

Corn

 

50

lower yield

LOEC

20

Sandberg & Allen 1975

Corn

 

67

2473

EC50

13.4

Woolson et al. 1971

Corn

 

80

40

EC50

16

Jacobs & Keeney 1970

Corn

 

90

91

NOEC

90

Jacobs et al. 1970

Corn

 

100

86

NOEC

100

Woolson 1972

Corn

 

125

lower yield

LOEC

50

Sandberg & Allen 1975

Cotton

 

25

48

EC50

5

Deuel & Swoboda 1972

Cotton

 

50

lower yield

LOEC

20

Ray 1975

Cotton

 

50

lower yield

LOEC

20

Ray 1975

Cotton

 

125

60

EC50

25

Deuel & Swoboda 1972

Cotton

 

196

lower yield

LOEC

78.4

Ray 1975

Grass

 

3.2

5

EC95

 

Millhollon 1970

Grass

 

45

025

LOEC

18

Weaver et al. 1984

Grass

 

90

50

EC50

18

Weaver et al. 1984

Grass

 

104

88

NOEC

104

Clements & Munson 1947

Oat

010

5

78

NOEC

5

Woolson et al. 1971

Oat

010

5

94

NOEC

5

Woolson et al. 1971

Oat

 

100

2

EC98

 

Jacobs et al. 1970

Oat

40290

165

5

EC95

 

Rosenfels & Crafts 1940

Oat

 

50

90

NOEC

50

Sandberg & Allen 1975

Oat

160340

250

5

EC95

 

Rosenfels & Crafts 1940

Oat

 

188

lower yield

LOEC

75.2

Cooper et al. 1931

Oat

280590

435

5

EC95

 

Rosenfels & Crafts 1940

Oat

540850

695

5

EC95

 

Rosenfels & Crafts 1940

Pea

1114

12.5

90

NOEC

12.5

Steevens et al. 1972

Pea

 

25

lower yield

LOEC

10

Walsh & Keeney 1975

Pea

2575

50

85

NOEC

50

Stewart & Smith 1922

Pea

045

22.5

90

NOEC

22.5

Jacobs & Keeney 1970

Pea

 

140

50

EC50

28

MacPhee et al. 1960

Pine

>200

200

lethal

NOEC

200

Sheppard et al. 1985

Pine

>250

250

lethal

NOEC

250

Sheppard et al. 1985

Pine

>500

500

no effect

NOEC

500

Sheppard et al. 1985

Potato

4573

59

85

NOEC

59

Sheppard et al. 1985

Potato

 

68

lower yield

LOEC

27.2

Walsh & Keeney 1975

Potato

 

75

33

EC50

15

Stewart & Smith 1922

Potato

 

180

79

LOEC

72

Jacobs & Keeney 1970

Radish

 

2.5

lower yield

LOEC

6.33

Hiltbold 1975

Radish

10100

55

2393

EC50

11

Woolson 1973

Radish

 

15

89

NOEC

15

Sheppard et al. 1985

Radish

 

36

52

EC50

7.2

Woolson & Isensee 1981

Radish

 

390

82

NOEC

390

Sheppard et al. 1982

Radish

 

500

86

NOEC

500

Stewart & Smith 1922

Sedge

 

1.8

lower yield

LOEC

0.72

Hiltbold 1975

Soyabean

 

12.5

55

EC50

2.5

Deuel & Swoboda 1972

Soyabean

 

34

lower yield

LOEC

13.6

Raab 1972a, 1972b

Soyabean

 

37

65

LOEC

14.8

Woolson & Isensee 1981

Soyabean

 

50

61

EC40

10

Sandberg & Allen 1975

Soyabean

 

84

60

EC40

16.8

Deuel & Swoboda 1972

Tomato

010

5

7794

NOEC

8.47

Woolson 1973

Tomato

 

140

76

LOEC

56

MacPhee et al. 1960

Tomato

 

514

90

NOEC

514

Clements & Munson 1947

Wheat

 

94

lower yield

LOEC

37.6

Cooper et al. 1931

Wheat

 

250

63

LOEC

100

Stewart & Smith 1922

NS= not statistically significant (P>0.05)


Table B2: Raw toxicity data for arsenic to soil invertebrates and terrestrial mammals with the corresponding toxicity values when they were converted to NOEC values.

Common name

Scientific name

Measure of toxicity

Toxicity data

(mg/kg)

Est. EC10

Source

Common rat

Rattus norvegicus

NOEC

10

10

US EPA 2007

Deer mouse

Peromyscus maniculatus

EC50

1600

320

US EPA 2007

Earthworm

Eisenia fetida

EC50

100

20

Langdon et al. 2003

Earthworm

Lumbriculus rubellus

EC50

1510

302

Langdon et al. 2001

Earthworm

L. rubellus

EC50

96

19.2

Langdon et al. 2001

Earthworm

L. terrestris

NOEC

100

100

Meharg et al. 1998

Earthworm

L. terrestris

NOEC

100

100

Meharg et al. 1998

Fulvous whistling duck

Dendrocygna bicolor

EC50

1145

229

Kegley et al. 2008

Northern bobwhite

Colinus virginianus

EC50

168.5

33.7

Kegley et al. 2008

Northern bobwhite

C. virginianus

EC50

432

86.4

Kegley et al. 2008

Sheep

Ovis aries

NOEC

25

25

US EPA 2007

 


There are two tables in this appendix (Tables C1 and C2).

Table C1. Raw data for naphthalene where the toxicity was expressed in terms of mg/kg.

Test species

Measure of toxicity

Toxic conc.

(mg/kg)

Source

Common name

Scientific name

Common rat

Rattus norvegicus

NOEC

1000

US EPA 2007

Earthworm

Eisenia fetida

EC25

54

CCME 1999b

European rabbit

Oryctolagus cuniculus

NOEC

2000

US EPA 2007

House mouse

Mus musculus

LD10

320

US EPA 2007

House mouse

M. musculus

LD10

518

US EPA 2007

Lettuce

Lactuca sativa

NOEC

100

Adema & Henzen 2001

Lettuce

L. sativa

NOEC

32

Adema & Henzen 2001

Lettuce

L. sativa

NOEC

100

Adema & Henzen 2001

Lettuce

L. sativa

NOEC

3.2

Adema & Henzen 2001

Lettuce

L. sativa

NOEC

32

Adema & Henzen 2001

Lettuce

L. sativa

EC25

3

CCME 1999b

Northern bobwhite

Colinus virginianus

NOEC

1000

US EPA 2007

Northern bobwhite

C. virginianus

NOEC

1000

US EPA 2007

Northern bobwhite

C. virginianus

LD50

538

US EPA 2007

Radish

Raphanus sativa

EC25

61

CCME 1999b

Springtail

Folsomia fimetaria

EC10

20

Sverdrup et al. 2002

LD10 = dose lethal to 10% of organisms.


Table C2: Raw toxicity data for naphthalene that caused a 50% effect (EC50) and was expressed in terms of g/m2, the corresponding value expressed in terms of mg/kg, the corresponding EC10 or NOEC values, and the source of the original data.

Test species

EC50

(g/m2)

EC50

(mg/kg)

Estimated NOEC or EC10

(mg/kg)

Source

Common name

Scientific name

Mite

Acari sp.

13

1000

200

Best et al. 1978

Mite

Acari sp.

11

846

169

Best et al. 1978

Mite

Acari sp.

24

1846

369

Best et al. 1978

Mite

Mesostigmata sp.

10

769

154

Best et al. 1978

Mite

Mesostigmata sp.

16

1231

246

Best et al. 1978

Mite

Oribatida sp.

10

769

153

Best et al. 1978

Mite

Oribatida sp.

24

1846

369

Best et al. 1978

Mite

Oribatida sp.

12

923

185

Best et al. 1978

Spider

Grammonota inornata

9

692

138

Best et al. 1978

Spider

G. inornata

17

1308

262

Best et al. 1978

Spider

G. inornata

10

769

154

Best et al. 1978

Springtail

Collembola sp.

8

615

123

Best et al. 1978

Springtail

Collembola sp.

21

1615

323

Best et al. 1978

Springtail

Collembola sp.

16

1231

246

Best et al. 1978

Springtail

Poduromorpha sp.

18

1385

277

Best et al. 1978

Springtail

Poduromorpha sp.

16

1231

246

Best et al. 1978

Springtail

Poduromorpha sp.

8

615

123

Best et al. 1978

 


Table D1:The raw toxicity data for DDT that measured a variety of toxic effects, the estimated NOEC or EC10 value, and the source.

Test species

Measure of toxicity

Toxic conc.

(mg/kg)

Est. NOEC or EC10 (mg/kg)

Source

Common name

Scientific name

Earthworm

Eisenia fetida

EC10

47.7

47.7

Hund-Rindke & Simon 2005

Earthworm

E. fetida

NOEC

1000

1000

Hund-Rindke & Simon 2005

Earthworm

E. fetida

NOEC

1000

1000

Hund-Rindke & Simon 2005

Field mustard

Brassica rapa

NOEC

1000

1000

Hund-Rindke & Simon 2005

Field mustard

B. rapa

NOEC

1000

1000

Hund-Rindke & Simon 2005

Field mustard

B. rapa

NOEC

1000

1000

Hund-Rindke & Simon 2005

Helmeted guineafowl

Numida meleagris

LOEC

75

30

US EPA 2007

House sparrow

Passer domesticus

LOEC

1500

600

US EPA 2007

Japanese quail

Coturnix japonica

LOEC

200

80

US EPA 2007

Mallard duck

Anas platyrhynchos

LOEC

59.5

23.8

US EPA 2007

Northern bobwhite

Colinus virginianus

NOEC

50

50

US EPA 2007

Northern bobwhite

C. virginianus

LOEC

232

92.8

US EPA 2007

Oats

Avena sativa

NOEC

1000

1000

Hund-Rindke & Simon 2005

Oats

A. sativa

NOEC

1000

1000

Hund-Rindke & Simon 2005

Oats

A. sativa

NOEC

1000

1000

Hund-Rindke & Simon 2005

Ring-necked pheasant

Phasianus colchicus

LC50

522

104

US EPA 2007

Soil process

Ammonification

EC12

1250

1250

CCME 1999a

Soil process

Nitrification

EC36

1000

400

CCME 1999a

Soil process

Nitrification

EC31

12.5

5

CCME1999a

Soil process

Nitrification

EC24

50

50

CCME 1999a

Soil process

Nitrification

EC22

100

100

CCME 1999a

Soil process

Potential ammonium oxidation

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

Potential ammonium oxidation

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

Potential ammonium oxidation

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

Respiration

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

Respiration

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

Respiration

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

SIR

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

SIR

NOEC

1000

1000

Hund-Rindke & Simon 2005

Soil process

SIR

NOEC

1000

1000

Hund-Rindke & Simon 2005

Springtail

Folsomia candida

EC10

99.9

99.9

Hund-Rindke & Simon 2005

Springtail

F. candida

NOEC

1000

1000

Hund-Rindke & Simon 2005

Springtail

F. candida

NOEC

1000

1000

Hund-Rindke & Simon 2005

 LC50 = the concentration that is lethal to 50% of the organisms.

Table E1: The raw toxicity data for copper and the ageing/leaching factors that were used in the derivation of the soil quality guidelines derived in this project, and the source of the toxicity data.

Species

End point

NOEC or EC10 added (mg/kg)

LOEC and EC30 (mg/kg)

EC50 added (mg/kg)

ALF

Reference

Andryala integrifolia

mortality

76

106

130

2

Brun et al. 2003

 

 

 

 

 

 

 

Andryala integrifolia

seedling emergence

78

106

128

2

Brun et al. 2003

 

 

 

 

 

 

 

Arachis hypogaea

grain yield

398

 

467

1

Barry & Bell 2006

Arachis hypogaea

grain yield

197

 

516

1

Barry & Bell 2006

 

 

 

 

 

 

 

Avena sativa

grain yield

200

300

600

2

De Haan et al. 1985

Avena sativa

grain yield

200

300

600

2

De Haan et al. 1985

Avena sativa

grain yield

200

300

600

2

De Haan et al. 1985

Avena sativa

grain yield

200

300

600

2

De Haan et al. 1985

Avena sativa

grain yield

200

300

600

2

De Haan et al. 1985

 

 

 

 

 

 

 

Brassica napus

grain yield

1310

1965

1370

1

Heemsbergen et al. 2007

Brassica napus

grain yield

926

1136

1566

1

NBRP unpublished data

Brassica napus

grain yield

315

473

452

1

Butler et al. 2007

 

 

 

 

 

 

 

Gossypium sp.

crop yield

1451

2177

1757

1

Barry & Bell 2006

 

 

 

 

 

 

 

Hordeum vulgare

grain yield

77

116

720

1

Heemsbergen et al. 2007

Hordeum vulgare

grain yield

313

470

1300

1

Heemsbergen et al. 2007

Hordeum vulgare

grain yield

222

333

645

1

Heemsbergen et al. 2007

Hordeum vulgare

grain yield

49

74

515

1

Butler et al. 2007

Hordeum vulgare

grain yield

28

41

227

1

Butler et al. 2007

 

 

 

 

 

 

 

Hordeum vulgare

seedling emergence

112

305

335

2

Ali et al. 2004

 

 

 

 

 

 

 

Hordeum vulgare

shoot weight

305

>304.8

914

2

Ali et al. 2004

 

 

 

 

 

 

 

Hordeum vulgare

root weight

3

11

305

2

Ali et al. 2004

Hordeum vulgare

root yield

58

87

137

2

Rooney et al. 2006

Hordeum vulgare

root yield

16

24

36

2

Rooney et al. 2006

Hordeum vulgare

root yield

85

128

173

2

Rooney et al. 2006

Hordeum vulgare

root yield

80

120

233

2

Rooney et al. 2006

Hordeum vulgare

root yield

45

68

536

2

Rooney et al. 2006

Hordeum vulgare

root yield

14

21

40

2

Rooney et al. 2006

Hordeum vulgare

root yield

83

125

161

2

Rooney et al. 2006

Hordeum vulgare

root yield

20

30

56

2

Rooney et al. 2006

Hordeum vulgare

root yield

35

53

129

2

Rooney et al. 2006

Hordeum vulgare

root yield

144

216

376

2

Rooney et al. 2006

Hordeum vulgare

root yield

69

104

187

2

Rooney et al. 2006

Hordeum vulgare

root yield

53

80

359

2

Rooney et al. 2006

Hordeum vulgare

root yield

77

116

252

2

Rooney et al. 2006

Hordeum vulgare

root yield

120

180

405

2

Rooney et al. 2006

Hordeum vulgare

root yield

96

144

344

2

Rooney et al. 2006

Hordeum vulgare

root yield

111

167

326

2

Rooney et al. 2006

Hordeum vulgare

root yield

98

147

375

2

Rooney et al. 2006

Hordeum vulgare

root yield

26

39

114

2

Rooney et al. 2006

 

 

 

 

 

 

 

Hypochoeris radicata

mortality

99

165

227

2

Brun et al. 2003

 

 

 

 

 

 

 

Hypochoeris radicata

reproduction

157

173

187

2

Brun et al. 2003

 

 

 

 

 

 

 

Hypochoeris radicata

seedling emergence

175

187

195

2

Brun et al. 2003

 

 

 

 

 

 

 

Lolium perenne

shoot yield

95

513

1036

2

Jarvis 1978

 

 

 

 

 

 

 

Lolium perenne

root yield

95

831

947

2

Jarvis 1978

 

 

 

 

 

 

 

Lycopersicon esculentum

shoot yield

46

69

130

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

159

239

427

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

370

555

829

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

48

72

115

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

29

44

61

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

89

134

237

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

179

269

281

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

598

897

851

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

252

378

351

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

311

467

933

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

481

722

795

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

212

318

771

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

212

318

659

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

251

377

444

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

116

174

429

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

70

105

325

2

Rooney et al. 2006

Lycopersicon esculentum

shoot yield

175

300

600

2

Rhoads et al. 1989

Lycopersicon esculentum

shoot yield

350

700

1400

2

Rhoads et al. 1989

Lycopersicon esculentum

shoot yield

350

700

1400

2

Rhoads et al. 1989

 

 

 

 

 

 

 

Panicum milaceum

yield

206

309

389

1

Barry & Bell 2006

 

 

 

 

 

 

 

Poa annua

mortality

200

389

418

2

Brun et al. 2003

 

 

 

 

 

 

 

Poa annua

reproduction

200

216

262

2

Brun et al. 2003

 

 

 

 

 

 

 

Poa annua

seedling emergence

100

91

141

2

Brun et al. 2003

 

 

 

 

 

 

 

Polygonum convolvulus

yield (total dm)

188

237

276

2

Kjær & Elmegaard 1996

Polygonum convolvulus

yield (total dm)

188

301

309

2

Kjær & Elmegaard 1996

 

 

 

 

 

 

 

Polygonum convolvulus

reproductive dry matter

188

222

251

2

Kjær & Elmegaard 1996

Polygonum convolvulus

reproductive dry matter

188

247

287

2

Kjær & Elmegaard 1996

 

 

 

 

 

 

 

Polygonum convolvulus

seed biomass

188

303

327

2

Kjær & Elmegaard 1996

 

 

 

 

 

 

 

Polygonum convolvulus

mortality

113

211

257

2

Kjær & Elmegaard 1996

Polygonum convolvulus

mortality

113

188

387

2

Kjær & Elmegaard 1996

 

 

 

 

 

 

 

Polygonum convolvulus

shoot yield

200

300

259

2

Pedersen et al. 2000

 

 

 

 

 

 

 

Polygonum convolvulus

root yield

200

300

291

2

Pedersen et al. 2000

 

 

 

 

 

 

 

Sacharum sp.

yield

203

305

342

1

Barry & Bell 2006

 

 

 

 

 

 

 

Senecio vulgaris

mortality

78

150

228

2

Brun et al. 2003

 

 

 

 

 

 

 

Senecio vulgaris

reproduction

156

173

184

2

Brun et al. 2003

 

 

 

 

 

 

 

Senecio vulgaris

seedling emergence

28

57

88

2

Brun et al. 2003

 

 

 

 

 

 

 

Sorghum sp.

yield

598

897

1433

1

Barry & Bell 2006

Sorghum sp.

yield

206

309

318

1

Barry & Bell 2006

 

 

 

 

 

 

 

Triticum aestivum

grain yield

1133

1139

1147

1

Warne et al. 2008a

Triticum aestivum

grain yield

132

176

286

1

Warne et al. 2008a

Triticum aestivum

grain yield

731

1561

5705

1

Warne et al. 2008a

Triticum aestivum

grain yield

148

228

476

1

Warne et al. 2008a

Triticum aestivum

grain yield

284

385

649

1

Warne et al. 2008a

Triticum aestivum

grain yield

130

157

212

1

Warne et al. 2008a

Triticum aestivum

grain yield

209

242

310

1

Warne et al. 2008a

Triticum aestivum

grain yield

787

1316

3170

1

Warne et al. 2008a

Triticum aestivum

grain yield

586

603

632

1

Warne et al. 2008a

Triticum aestivum

grain yield

622

752

1040

1

Warne et al. 2008a

Triticum aestivum

grain yield

473

768

1760

1

Warne et al. 2008a

 

 

 

 

 

 

 

Triticum aestivum

8wk plant biomass

3

36

2070

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

351

360

375

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

635

792

1154

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

117

168

315

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

193

220

272

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

144

233

526

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

40

75

223

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

1100

1128

1183

1

Warne et al. 2008a

Triticum aestivum

8wk plant biomass

52

102

330

1

Warne et al. 2008a

 

 

 

 

 

 

 

Tritosecale sp.

yield

481

1020

2040

1

Butler et al. 2007

 

 

 

 

 

 

 

Zea mays

yield

274

 

363

1

Barry & Bell 2006

 

 

 

 

 

 

 

Cognettia sphagnetorum

growth

20

50

91

2

Augustsson & Rundgren 1998

Cognettia sphagnetorum

growth

63

85

167

2

Augustsson & Rundgren 1998

Cognettia sphagnetorum

growth

441

502

605

2

Augustsson & Rundgren 1998

Cognettia sphagnetorum

growth

312

435

557

2

Augustsson & Rundgren 1998

 

 

 

 

 

 

 

Cognettia sphagnetorum

fragmentation

455

538

676

2

Augustsson & Rundgren 1998

Cognettia sphagnetorum

fragmentation

23

82

 

2

Augustsson & Rundgren 1998

 

 

 

 

 

 

 

Eisenia andrei

growth

56

84

168

2

van Dis et al. 1988

Eisenia andrei

growth

56

84

168

2

van Gestel et al. 1991

 

 

 

 

 

 

 

Eisenia andrei

reproduction

120

180

360

2

van Gestel et al. 1989

Eisenia andrei

reproduction

100

223

327

2

Kula & Larink 1997

Eisenia andrei

reproduction

100

168

240

2

Kula & Larink 1997

Eisenia andrei

reproduction

3

45

79

2

Kula & Larink 1997

Eisenia andrei

reproduction

154

 

 

2

Criel et al. 2008

Eisenia andrei

reproduction

88

188

264

2

Svendsen & Weeks 1997a

 

 

 

 

 

 

 

Eisenia andrei

mortality

188

335

564

2

Svendsen & Weeks 1997a

 

 

 

 

 

 

 

Eisenia fetida

mortality

208

311

555

2

Spurgeon et al. 1994

Eisenia fetida

mortality

293

440

836

2

Spurgeon & Hopkin 1995

 

 

 

 

 

 

 

Eisenia fetida

growth

725

1088

601

2

Spurgeon & Hopkin 1995

Eisenia fetida

growth

700

1000

 

2

Scott-Fordsmand et al. 2000

 

 

 

 

 

 

 

Eisenia fetida

reproduction

30

44

51

2

Spurgeon et al. 1994

Eisenia fetida

reproduction

29

44

87

2

Spurgeon & Hopkin 1995

Eisenia fetida

reproduction

10

132

174

2

Kula & Larink 1997

Eisenia fetida

reproduction

32

72

108

2

Kula & Larink 1997

Eisenia fetida

reproduction

2

13

42

2

Kula & Larink 1997

Eisenia fetida

reproduction

0

3

10

2

Kula & Larink 1997

Eisenia fetida

reproduction

100

300

210

2

Scott-Fordsmand et al. 2000

Eisenia fetida

reproduction

161

243

190

2

Criel et al. 2008

Eisenia fetida

reproduction

84

172

211

2

Criel et al. 2008

Eisenia fetida

reproduction

120

92

708

2

Criel et al. 2008

Eisenia fetida

reproduction

86

100

171

2

Criel et al. 2008

Eisenia fetida

reproduction

88

289

296

2

Criel et al. 2008

Eisenia fetida

reproduction

67

165

198

2

Criel et al. 2008

Eisenia fetida

reproduction

31

94

67

2

Criel et al. 2008

Eisenia fetida

reproduction

213

464

329

2

Criel et al. 2008

Eisenia fetida

reproduction

195

237

230

2

Criel et al. 2008

Eisenia fetida

reproduction

279

538

487

2

Criel et al. 2008

Eisenia fetida

reproduction

151

501

267

2

Criel et al. 2008

Eisenia fetida

reproduction

346

501

407

2

Criel et al. 2008

Eisenia fetida

reproduction

148

281

309

2

Criel et al. 2008

Eisenia fetida

reproduction

454

258

731

2

Criel et al. 2008

Eisenia fetida

reproduction

188

160

358

2

Criel et al. 2008

Eisenia fetida

reproduction

69

153

149

2

Criel et al. 2008

Eisenia fetida

reproduction

223

361

347

2

Criel et al. 2008

 

 

 

 

 

 

 

Lumbricus rubellus

mortality

150

224

486

2

Svendsen & Weeks 1997b

Lumbricus rubellus

mortality

117

344

393

2

Ma 1984

Lumbricus rubellus

mortality

123

359

408

2

Ma 1984

Lumbricus rubellus

mortality

150

 

459

2

Ma 1982

Lumbricus rubellus

mortality

447

521

1384

2

Spurgeon et al. 2004

 

 

 

 

 

 

 

Lumbricus rubellus

litter breakdown

40

123

162

2

Ma 1984

Lumbricus rubellus

litter breakdown

50

168

189

2

Ma 1984

 

 

 

 

 

 

 

Lumbricus rubellus

growth

117

358

393

2

Ma 1984

Lumbricus rubellus

growth

73

150

228

2

Svendsen & Weeks 1997b

Lumbricus rubellus

growth

140

642

462

2

Spurgeon et al. 2004

 

 

 

 

 

 

 

Lumbricus rubellus

reproduction

40

97

162

2

Ma 1984

 

 

 

 

 

 

 

Plectus acuminatus

reproduction

32

100

300

2

Kammenga et al. 1996

 

 

 

 

 

 

 

Folsomia candida

reproduction

190

299

260

2

Criel et al. 2008

Folsomia candida

reproduction

10

49

43

2

Criel et al. 2008

Folsomia candida

reproduction

417

530

952

2

Criel et al. 2008

Folsomia candida

reproduction

1380

2070

2200

2

Criel et al. 2008

Folsomia candida

reproduction

50

75

166

2

Criel et al. 2008

Folsomia candida

reproduction

51

85

112

2

Criel et al. 2008

Folsomia candida

reproduction

206

314

325

2

Criel et al. 2008

Folsomia candida

reproduction

186

489

325

2

Criel et al. 2008

Folsomia candida

reproduction

618

551

1238

2

Criel et al. 2008

Folsomia candida

reproduction

195

285

510

2

Criel et al. 2008

Folsomia candida

reproduction

659

803

862

2

Criel et al. 2008

Folsomia candida

reproduction

80

291

434

2

Criel et al. 2008

Folsomia candida

reproduction

1186

1666

1626

2

Criel et al. 2008

Folsomia candida

reproduction

550

707

845

2

Criel et al. 2008

Folsomia candida

reproduction

200

311

640

2

Criel et al. 2008

Folsomia candida

reproduction

683

1629

1199

2

Criel et al. 2008

Folsomia candida

reproduction

686

919

835

2

Criel et al. 2008

Folsomia candida

reproduction

227

1049

632

2

Criel et al. 2008

Folsomia candida

reproduction

16

37

73

2

Criel et al. 2008

Folsomia candida

reproduction

797

 

813

2

Herbert et al. 2004

Folsomia candida

reproduction

198

411

650

2

Sandifer & Hopkin 1996

Folsomia candida

reproduction

231

486

774

2

Sandifer & Hopkin 1996

Folsomia candida

reproduction

920

1083

1200

2

Sandifer & Hopkin 1996

Folsomia candida

reproduction

200

300

700

2

Sandifer & Hopkin 1997

Folsomia candida

reproduction

200

300

640

2

Sandifer & Hopkin 1997

Folsomia candida

reproduction

400

600

1200

2

Rundgren & van Gestel 1988

Folsomia candida

reproduction

400

600

1200

2

Rundgren & van Gestel 1988

 

 

 

 

 

 

 

Folsomia candida

mortality

1281

1821

2271

2

Sandifer & Hopkin 1997

Folsomia candida

mortality

387

981

1761

2

Sandifer & Hopkin 1997

Folsomia candida

mortality

135

676

1859

2

Sandifer & Hopkin 1997

Folsomia candida

mortality

135

676

 

2

Sandifer & Hopkin 1996

Folsomia candida

mortality

561

1586

 

2

Sandifer & Hopkin 1996

Folsomia candida

mortality

2657

2978

 

2

Sandifer & Hopkin 1996

 

 

 

 

 

 

 

Folsomia candida

growth

800

1200

2400

2

Rundgren & van Gestel 1988

Folsomia candida

growth

200

300

600

2

Rundgren & van Gestel 1988

 

 

 

 

 

 

 

Folsomia fimetaria

mortality

878

1000

2000

2

Scott-Fordsmand et al. 1997

Folsomia fimetaria

mortality

1000

>1000

3000

2

Scott-Fordsmand et al. 1997

Folsomia fimetaria

mortality

1000

>1000

3000

2

Scott-Fordsmand et al. 1997

 

 

 

 

 

 

 

Folsomia fimetaria

growth

542

400

800

2

Scott-Fordsmand et al. 1997

Folsomia fimetaria

growth

845

800

1600

2

Scott-Fordsmand et al. 1997

Folsomia fimetaria

growth

527

600

1200

2

Scott-Fordsmand et al. 1997

 

 

 

 

 

 

 

Folsomia fimetaria

reproduction

38

57

113

2

Scott-Fordsmand et al. 1997

Folsomia fimetaria

reproduction

122

183

638

2

Pedersen et al. 2000

Folsomia fimetaria

reproduction

698

1047

1225

2

Pedersen et al. 2001a

Folsomia fimetaria

reproduction

776

1164

1635

2

Pedersen et al. 2001a

Folsomia fimetaria

reproduction

888

1332

1674

2

Pedersen et al. 2001a

Folsomia fimetaria

reproduction

648

972

1259

2

Pedersen et al. 2001a

Folsomia fimetaria

reproduction

688

1032

1395

2

Pedersen et al. 2001a

 

 

 

 

 

 

 

Hypoaspis aculeifer

reproduction

174

261

522

2

Krogh & Axelsen 1998

 

 

 

 

 

 

 

Isotoma viridis

growth

50

75

150

2

Rundgren & van Gestel 1988

Isotoma viridis

growth

400

600

1200

2

Rundgren & van Gestel 1988

 

 

 

 

 

 

 

Platynothrus peltifer

reproduction

63

95

189

2

van Gestel & Doornekamp 1998

Platynothrus peltifer

reproduction

63

95

189

2

van Gestel & Doornekamp 1998

Platynothrus peltifer

reproduction

63

95

189

2

van Gestel & Doornekamp 1998

 

 

 

 

 

 

 

Soil microbial process

microbial biomass C

118

268

354

2

Khan & Scullion 2002

Soil microbial process

microbial biomass C

118

268

354

2

Khan & Scullion 2002

 

 

 

 

 

 

 

Soil microbial process

microbial biomass N

468

768

1404

2

Khan & Scullion 2002

Soil microbial process

microbial biomass N

<118

118

236

2

Khan & Scullion 2002

 

 

 

 

 

 

 

Soil microbial process

SIR1

635

953

1905

2

Speir et al. 1999

Soil microbial process

SIR

635

953

1905

2

Speir et al. 1999

Soil microbial process

SIR

1200

1800

3600

2

University of Leuven 2004

Soil microbial process

SIR

150

225

450

2

University of Leuven 2004

Soil microbial process

SIR

50

75

150

2

University of Leuven 2004

Soil microbial process

SIR

600

900

1800

2

University of Leuven 2004

Soil microbial process

SIR

100

150

300

2

University of Leuven 2004

Soil microbial process

SIR

25

38

75

2

University of Leuven 2004

Soil microbial process

SIR

100

150

300

2

University of Leuven 2004

Soil microbial process

SIR

50

75

150

2

University of Leuven 2004

Soil microbial process

SIR

25

38

75

2

University of Leuven 2004

Soil microbial process

SIR

400

600

1200

2

University of Leuven 2004

Soil microbial process

SIR

300

450

900

2

University of Leuven 2004

Soil microbial process

SIR

50

75

150

2

University of Leuven 2004

Soil microbial process

SIR

102

153

306

2

University of Leuven 2004

Soil microbial process

SIR

200

300

600

2

University of Leuven 2004

Soil microbial process

SIR

89

134

267

2

University of Leuven 2004

Soil microbial process

SIR

23

35

69

2

University of Leuven 2004

Soil microbial process

SIR

300

450

900

2

University of Leuven 2004

Soil microbial process

SIR

200

300

600

2

University of Leuven 2004

Soil microbial process

SIR

50

75

150

2

University of Leuven 2004

Soil microbial process

SIR

170

255

510

2

University of Leuven 2004

Soil microbial process

SIR

12

18

36

2

University of Leuven 2004

Soil microbial process

SIR

25

38

75

2

University of Leuven 2004

Soil microbial process

SIR

100

150

300

2

University of Leuven 2004

Soil microbial process

SIR

27

41

81

2

University of Leuven 2004

Soil microbial process

SIR

185

345

1000

1

Broos et al. 2007

Soil microbial process

SIR

3

31

1078

1

Broos et al. 2007

Soil microbial process

SIR

326

450

555

1

Broos et al. 2007

Soil microbial process

SIR

230

496

1842

1

Broos et al. 2007

Soil microbial process

SIR

255

503

1606

1

Broos et al. 2007

Soil microbial process

SIR

48

134

784

1

Broos et al. 2007

Soil microbial process

SIR

39

111

662

1

Broos et al. 2007

Soil microbial process

SIR

222

559

2321

1

Broos et al. 2007

Soil microbial process

SIR

202

421

1478

1

Broos et al. 2007

Soil microbial process

SIR

26

73

431

1

Broos et al. 2007

Soil microbial process

SIR

134

259

795

1

Broos et al. 2007

Soil microbial process

SIR

25

97

940

1

Broos et al. 2007

 

 

 

 

 

 

 

Soil microbial process

GAD2

55

400

800

1

Haanstra & Doelman 1984

Soil microbial process

GAD

55

400

800

1

Haanstra & Doelman 1984

Soil microbial process

GAD

400

1000

2000

1

Haanstra & Doelman 1984

 

 

 

 

 

 

 

Soil microbial process

MRR3

2400

3600

7200

2

University of Leuven 2004

Soil microbial process

MRR

1200

1800

3600

2

University of Leuven 2004

Soil microbial process

MRR

1200

1800

3600

2

University of Leuven 2004

Soil microbial process

MRR

300

450

900

2

University of Leuven 2004

Soil microbial process

MRR

50

75

150

2

University of Leuven 2004

Soil microbial process

MRR

200

300

600

2

University of Leuven 2004

Soil microbial process

MRR

100

150

300

2

University of Leuven 2004

Soil microbial process

MRR

50

75

150

2

University of Leuven 2004

Soil microbial process

MRR

400

600

1200

2

University of Leuven 2004

Soil microbial process

MRR

150

225

450

2

University of Leuven 2004

Soil microbial process

MRR

50

75

150

2

University of Leuven 2004

Soil microbial process

MRR

400

600

1200

2

University of Leuven 2004

Soil microbial process

MRR

600

900

1800

2

University of Leuven 2004

Soil microbial process

MRR

150

225

450

2

University of Leuven 2004

Soil microbial process

MRR

150

225

450

2

University of Leuven 2004

Soil microbial process

MRR

51

77

153

2

University of Leuven 2004

Soil microbial process

MRR

83

125

249

2

University of Leuven 2004

Soil microbial process

MRR

100

150

300

2

University of Leuven 2004

Soil microbial process

MRR

 

144

288

2

Oorts et al. 2006a

Soil microbial process

MRR

 

348

696

2

Oorts et al. 2006a

Soil microbial process

MRR

 

802

1604

2

Oorts et al. 2006a

 

 

 

 

 

 

 

Soil microbial process

respiration

89

1402

7932

1

Doelman & Haanstra 1984

Soil microbial process

respiration

400

600

1200

1

Doelman & Haanstra 1984

Soil microbial process

respiration

493

4097

15477

1

Doelman & Haanstra 1984

Soil microbial process

respiration

32

219

730

1

Doelman & Haanstra 1984

 

 

 

 

 

 

 

Soil microbial process

PNR4

200

300

400

2

University of Leuven 2004

Soil microbial process

PNR

1200

1800

2400

2

University of Leuven 2004

Soil microbial process

PNR

25

38

50

2

University of Leuven 2004

Soil microbial process

PNR

25

38

50

2

University of Leuven 2004

Soil microbial process

PNR

50

75

100

2

University of Leuven 2004

Soil microbial process

PNR

100

150

200

2

University of Leuven 2004

Soil microbial process

PNR

300

450

600

2

University of Leuven 2004

Soil microbial process

PNR

200

300

400

2

University of Leuven 2004

Soil microbial process

PNR

800

1200

1600

2

University of Leuven 2004

Soil microbial process

PNR

400

600

800

2

University of Leuven 2004

Soil microbial process

PNR

600

900

1200

2

University of Leuven 2004

Soil microbial process

PNR

800

1200

1600

2

University of Leuven 2004

Soil microbial process

PNR

300

450

600

2

University of Leuven 2004

Soil microbial process

PNR

400

600

800

2

University of Leuven 2004

Soil microbial process

PNR

52

78

104

2

University of Leuven 2004

Soil microbial process

PNR

127

191

254

2

University of Leuven 2004

Soil microbial process

PNR

65

98

130

2

University of Leuven 2004

Soil microbial process

PNR

100

150

200

2

University of Leuven 2004

Soil microbial process

PNR

50

75

100

2

University of Leuven 2004

Soil microbial process

PNR

 

 

771

2

Oorts et al. 2006a

Soil microbial process

PNR

 

 

677

2

Oorts et al. 2006a

 

 

 

 

 

 

 

Soil microbial process

SIN6

100

150

200

2

Quraishi & Cornfield 1973

Soil microbial process

SIN

100

150

200

2

Quraishi & Cornfield 1973

Soil microbial process

SIN

1000

1500

2000

2

Premi & Cornfield 1969

Soil microbial process

SIN

2594

2594

2594

1

Broos et al. 2007

Soil microbial process

SIN

34

254

1078

1

Broos et al. 2007

Soil microbial process

SIN

206

208

211

1

Broos et al. 2007

Soil microbial process

SIN

1271

1451

1821

1

Broos et al. 2007

Soil microbial process

SIN

175

228

355

1

Broos et al. 2007

Soil microbial process

SIN

1

5

59

1

Broos et al. 2007

Soil microbial process

SIN

47

70

140

1

Broos et al. 2007

Soil microbial process

SIN

383

502

797

1

Broos et al. 2007

Soil microbial process

SIN

887

914

964

1

Broos et al. 2007

Soil microbial process

SIN

919

932

953

1

Broos et al. 2007

Soil microbial process

SIN

502

571

712

1

Broos et al. 2007

Soil microbial process

SIN

141

225

497

1

Broos et al. 2007

 

 

 

 

 

 

 

Soil microbial process

N-mineralisation

100

150

300

2

Quraishi & Cornfield 1973

Soil microbial process

N-mineralisation

268

465

804

2

Khan & Scullion 2002

Soil microbial process

N-mineralisation

 

115

230

2

Khan & Scullion 2002

 

 

 

 

 

 

 

Soil microbial process

ammonification

1000

1500

3000

2

Premi & Cornfield 1969

 

 

 

 

 

 

 

Soil microbial process

denitrification

100

250

300

2

Bollag & Barabasz 1979

1 SIR = substrate induced nitrification, 2 GAD = glutamic acid decomposition, 3 MRR = maize residue respiration, 4 PNR = potential nitrification rate, 5 SIN = substrate induced respiration.

 

A total of ten normalisation relationships were used to normalise the Cu toxicity data. The same ten normalisation relationships were used to generate the soil-specific ACLs. The generated soil-specific ACLs are the concentrations for each species/soil process that correspond to the desired level of protection (for example, 80% for urban residential land/public open space land use). Therefore, in order to provide the desired level of protection, the lowest ACL at each soil property value must be adopted as the final ACL.

 

For Cu there were six normalisation relationships based on CEC. These were for H. vulgare, L. escultentum, E. fetida, F. candida, F. fimetaria and PNR. Of these, PNR always generated the lowest ACL when the CEC was less than 10 cmolc/kg. At all higher CEC values the H. vulgare normalisation relationship always resulted in the lowest ACL. Therefore, one set of soil-specific ACLs was generated by for H. vulgare and another for PNR with the lowest of the two at each CEC being adopted as the CEC-based ACL values for Cu.

 

In addition, there was one normalisation relationship based on a combination of soil pH and organic carbon content (OC)for T. aestivum. There were also two normalisation relationships for SIN and MRM that were based on soil pH and one for SIR based on OC. The MRM normalisation relationship was not used as it had a negative relationship with toxicity, which was inconsistent with all the other normalisation relationships for Cu and all other elements. The SIN normalisation relationship always generated ACL values lower than those generated by the T. aestivum relationship at soil pH values up to 5.5. At higher soil pH values the situation was reversed. In addition, the ACLs generated by the SIR relationship (based on OC) were lower than all the ACLs generated by the T. aestivum relationship except when the OC was set at 1 in the T. aestivum relationship. Therefore one set of soil-specific ACLs was generated for T. aestivum and another for SIN with the lowest of the two at each pH being adopted as the CEC-pH-based ACL values for Cu.

 

The pH and CEC-based ACLs for Cu were presented in tables in this Schedule. The actual ACL values that apply for Cu are the lowest of either the pH-based ACLs or the CEC-based ACLs, depending on the properties of the soil in question.

Table G1: The raw toxicity data for lead and the ageing/leaching factors that were used in the derivation of the soil quality guidelines derived in this project, and the source of the toxicity data.

Species

End point

NOEC or EC10 (added)

LOEC and EC30 (added)

EC50 (added)

ALF

References

Avena sativa

root yield

100

500

300

4.2

Khan & Frankland 1984

 

 

 

 

 

 

 

Hordeum vulgare

shoot yield

50

250

1270

4.2

Aery & Jagetiya 1997

 

 

 

 

 

 

 

Lactuca sativa

shoot yield

432

648

2553

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

1172

1758

107

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

457

686

960

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

5120

7680

7500

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

132

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

141

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

240

4.2

Stevens et al, 2003

Lactuca sativa

shoot yield

 

 

847

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

807

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

731

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

2290

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

2630

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

3090

4.2

Stevens et al. 2003

Lactuca sativa

shoot yield

 

 

3100

4.2

Stevens et al. 2003

 

 

 

 

 

 

 

Lactuca sativa

germination

125

188

174

4.2

Vaughan & Greenslade 1998

 

 

 

 

 

 

 

Picea rubens

net photosynthesis

141

212

1228

4.2

Seiler & Paganelli 1987

 

 

 

 

 

 

 

Pinus taeda

root yield

546

819

659

4.2

Seiler & Paganelli 1987

 

 

 

 

 

 

 

Raphanus sativus

root yield

100

500

1800

4.2

Khan & Frankland 1983

 

 

 

 

 

 

 

Raphanus sativus

chlorophyll

100

500

300

4.2

Zaman & Zereen 1998

 

 

 

 

 

 

 

Triticum aestivum

net photosynthesis

1138

1707

5613

4.2

Waegeneers et al. 2004

Triticum aestivum

net photosynthesis

2064

3096

5037

4.2

Waegeneers et al. 2004

Triticum aestivum

net photosynthesis

1614

2421

5200

4.2

Waegeneers et al. 2004

 

 

 

 

 

 

 

Triticum aestivum

root yield

250

500

750

4.2

Khan & Frankland 1984

 

 

 

 

 

 

 

Zea mays

root length

100

150

300

4.2

LDA 2008

 

 

 

 

 

 

 

Dendrobaena rubida

hatching success

129

194

387

4.2

Bengtsson et al. 1986

 

 

 

 

 

 

 

Eisenia andrei

survival

1000

1500

3410

4.2

Vaughan & Greenslade 1998

 

 

 

 

 

 

 

Eisenia fetida

reproduction

608

912

1629

4.2

Spurgeon &  Hopkin 1995

Eisenia fetida

reproduction

1810

2715

3760

4.2

Spurgeon et al. 1994

Eisenia fetida

reproduction

400

600

1200

4.2

Davies et al. 2003a

Eisenia fetida

reproduction

3000

4500

9000

4.2

Davies et al. 2003b

 

 

 

 

 

 

 

Folsomia candida

reproduction

2000

5000

1360

4.2

Sandifer & Hopkin 1996

Folsomia candida

reproduction

400

2000

2970

4.2

Sandifer & Hopkin 1996

Folsomia candida

reproduction

2000

3000

3160

4.2

Sandifer & Hopkin 1996

Folsomia candida

reproduction

400

2000

1570

4.2

Sandifer & Hopkin 1997

Folsomia candida

reproduction

 

 

2970

4.2

Sandifer & Hopkin 1997

Folsomia candida

reproduction

1300

1950

1900

4.2

Bongers et al. 2004

Folsomia candida

reproduction

1138

1707

3414

4.2

Waegeneers et al. 2004

Folsomia candida

reproduction

2064

3096

6192

4.2

Waegeneers et al. 2004

Folsomia candida

reproduction

1614

2421

4842

4.2

Waegeneers et al. 2004

Folsomia candida

reproduction

 

 

2560

4.2

Waegeneers et al. 2004

 

 

 

 

 

 

 

Lumbriculus rubellus

growth

1000

1500

3000

4.2

Ma, 1982

 

 

 

 

 

 

 

Denitrification

 

250

500

750

4.2

Bollag & Barabasz 1979

 

 

 

 

 

 

 

Nitrification

 

448

672

1344

4.2

Waegeneers et al. 2004

Nitrification

 

2064

3096

6192

4.2

Waegeneers et al. 2004

Nitrification

 

253

380

759

4.2

Waegeneers et al. 2004

 

 

 

 

 

 

 

N-mineralisation

 

200

300

600

4.2

Chang & Broadbent 1982

N-mineralisation

 

1000

4000

3000

4.2

Wilke 1989

 

 

 

 

 

 

 

Respiration

 

188

282

564

4.2

Doelman & Haanstra 1979

Respiration

 

1500

2250

4500

4.2

Doelman & Haanstra 1979

Respiration

 

750

1125

2250

4.2

Doelman & Haanstra 1979

Respiration

 

1000

1500

3000

4.2

Doelman & Haanstra 1984

Respiration

 

150

225

450

4.2

Doelman & Haanstra 1984

Respiration

 

400

600

1200

4.2

Doelman & Haanstra 1984

Respiration

 

93

140

400

4.2

Chang & Broadbent 1981

Respiration

 

100

150

300

4.2

Saviozzi et al. 1997

Respiration

 

4144

6216

12432

4.2

Speir et al. 1999

Respiration

 

2279

3419

6838

4.2

Frostegård et al. 1993

 

 

 

 

 

 

 

Substrate-induced respiration

 

2072

3108

6216

4.2

Speir et al. 1999

Substrate-induced respiration

 

1450

2175

4350

4.2

Speir et al. 1999

 

 

 

 

 

 

 

ATP

 

 

 

3108

4.2

Frostegård et al. 1993

 


Table H1: The raw toxicity data for nickel and the ageing/leaching factors that were used in the derivation of the soil quality guidelines derived in this project, and the source of the toxicity data.

Species

Endpoint

NOEC & EC10 added (mg/kg)

Collated LOEC & EC30 added (mg/kg)

Collated EC50 added (mg/kg)

ALF

References

Lycopersicon esculentum

shoot yield

21

31.5

63

1.01

Rothamsted 2005

Lycopersicon esculentum

shoot yield

599

898.5

1797

1.02

Rothamsted 2005

Lycopersicon esculentum

shoot yield

16

24

48

1.02

Rothamsted 2005

Lycopersicon esculentum

shoot yield

125

187.5

375

1.02

Rothamsted 2005

Lycopersicon esculentum

shoot yield

10

15

30

1.03

Rothamsted 2005

Lycopersicon esculentum

shoot yield

42

63

126

1.07

Rothamsted 2005

Lycopersicon esculentum

shoot yield

52

78

156

1.14

Rothamsted 2005

Lycopersicon esculentum

shoot yield

150

225

450

1.28

Rothamsted 2005

Lycopersicon esculentum

shoot yield

118

177

354

1.66

Rothamsted 2005

Lycopersicon esculentum

shoot yield

250

375

750

2.00

Rothamsted 2005

Lycopersicon esculentum

shoot yield

200

300

600

3.32

Rothamsted 2005

Lycopersicon esculentum

shoot yield

504

756

1512

3.01

Rothamsted 2005

Lycopersicon esculentum

shoot yield

224

336

672

3.32

Rothamsted 2005

Lycopersicon esculentum

shoot yield

144

216

432

3.32

Rothamsted 2005

Lycopersicon esculentum

shoot yield

189

283.5

567

3.66

Rothamsted 2005

 

 

 

 

 

 

 

Hordeum vulgare

root yield

31

46.5

93

1.01

Rothamsted 2005

Hordeum vulgare

root yield

1101

1651.5

3303

1.02

Rothamsted 2005

Hordeum vulgare

root yield

90

135

270

1.02

Rothamsted 2005

Hordeum vulgare

root yield

249

373.5

747

1.02

Rothamsted2005

Hordeum vulgare

root yield

46

69

138

1.03

Rothamsted 2005

Hordeum vulgare

root yield

123

184.5

369

1.07

Rothamsted 2005

Hordeum vulgare

root yield

261

391.5

783

1.14

Rothamsted 2005

Hordeum vulgare

root yield

128

192

384

1.14

Rothamsted 2005

Hordeum vulgare

root yield

398

597

1194

1.28

Rothamsted 2005

Hordeum vulgare

root yield

106

159

318

1.66

Rothamsted 2005

Hordeum vulgare

root yield

211

316.5

633

2.00

Rothamsted 2005

Hordeum vulgare

root yield

268

402

804

3.32

Rothamsted 2005

Hordeum vulgare

root yield

289

433.5

867

3.01

Rothamsted 2005

Hordeum vulgare

root yield

587

880.5

1761

3.32

Rothamsted 2005

Hordeum vulgare

root yield

96

144

288

3.32

Rothamsted 2005

Hordeum vulgare

root yield

304

456

912

3.66

Rothamsted 2005

 

 

 

 

 

 

 

Spinach

yield

10

21.7

32.7

1.03

Willaert & Verloo 1988

Spinach

yield

100

40

40

5.66

Willaert & Verloo 1988

Spinach

yield

 

200

200

5.66

Willaert & Verloo 1988

 

 

 

 

 

 

 

Avena sativa

grain yield

500

750

1500

2.32

Halstead et al. 1969

Avena sativa

grain yield

20

51

56.2

1.12

Halstead et al. 1969

Avena sativa

grain yield

50

75.7

100

1.12

Halstead et al. 1969

Avena sativa

grain yield

50

55.4

63.1

1.38

Halstead et al. 1969

Avena sativa

grain yield

50

82.2

100

1.33

Halstead et al. 1969

Avena sativa

grain yield

100

144

159

1.08

Halstead et al. 1969

Avena sativa

grain yield

100

144

159

1.07

Halstead et al. 1969

Avena sativa

grain yield

100

144

159

1.43

Halstead et al. 1969

Avena sativa

grain yield

100

144

159

1.28

Halstead et al. 1969

Avena sativa

grain yield

66

99

198

1.14

De Haan et al. 1985

Avena sativa

grain yield

45

67.5

135

1.11

De Haan et al. 1985

Avena sativa

grain yield

47

70.5

141

1.08

De Haan et al. 1985

Avena sativa

grain yield

16

24

48

1.06

De Haan et al. 1985

Avena sativa

grain yield

40

60

120

1.11

De Haan et al. 1985

 

 

 

 

 

 

 

Avena sativa

yield

80

171

241

3.01

Liang & Schoenau 1995

Avena sativa

yield

>160

160

160

3.01

Liang & Schoenau 1995

 

 

 

 

 

 

 

Medicago sativa

EC10y(t)

100

366

404

3.32

Halstead et al. 1969

Medicago sativa

EC10y(t)

100

389

423

2.32

Halstead et al. 1969

Medicago sativa

EC10y(t)

20

19.1

20.9

1.12

Halstead et al. 1969

Medicago sativa

EC10y(t)

20

47.6

49.9

1.38

Halstead et al. 1969

Medicago sativa

EC10y(t)

20

40.5

42.3

1.33

Halstead et al. 1969

Medicago sativa

EC10y(t)

20

43.5

45.5

1.08

Halstead et al. 1969

Medicago sativa

EC10y(t)

50

101

106

1.07

Halstead et al. 1969

Medicago sativa

EC10y(t)

20

45.6

48.2

1.43

Halstead et al. 1969

Medicago sativa

EC10y(t)

50

100

118

1.28

Halstead et al. 1969

 

 

 

 

 

 

 

Raphanus sativus

yield

80

100.8

115

3.01

Liang & Schoenau 1995

Raphanus sativus

yield

>160

160

160

 

Liang & Schoenau 1995

 

 

 

 

 

 

 

Allium cepa

yield

46

73.1

103.4

7.17

Dang et al. 1990

 

 

 

 

 

 

 

Trigonella poenumgraceum

yield

84

132.8

176.6

7.17

Dang et al. 1990

 

 

 

 

 

 

 

Lolium perenne

yield

110

134.8

153.3

1.25

Frossard et al. 1989

 

 

 

 

 

 

 

Lactuca sativa

leaf yield

13

41

50.1

1.05

Gupta et al. 1987

Lactuca sativa

leaf yield

155

260

316

1.14

Gupta et al. 1987

Lactuca sativa

leaf yield

230

412

501

3.66

Gupta et al. 1987

Lactuca sativa

leaf yield

334

653

794

1.57

Gupta et al. 1987

Lactuca sativa

yield

40

77.5

99.5

3.01

Liang & Schoenau 1995

 

 

 

 

 

 

 

Zea mays

yield

120

164

200

4.53

Metwally & Rabie 1989

Zea mays

yield

40

107

158

6.37

Metwally & Rabie 1989

 

 

 

 

 

 

 

Folsomia candida

reproduction

36.4

54.6

109.2

1.01

University of Ghent/Euras 2005

Folsomia candida

reproduction

558

837

1674

1.02

University of Ghent/Euras 2005

Folsomia candida

reproduction

120

180

360

1.02

University of Ghent/Euras 2005

Folsomia candida

reproduction

527

790.5

1581

1.02

University of Ghent/Euras 2005

Folsomia candida

reproduction

104

156

312

1.03

University of Ghent/Euras 2005

Folsomia candida

reproduction

101

151.5

303

1.14

University of Ghent/Euras 2005

Folsomia candida

reproduction

180

270

540

1.14

University of Ghent/Euras 2005

Folsomia candida

reproduction

622

933

1866

1.28

University of Ghent/Euras 2005

Folsomia candida

reproduction

269

403.5

807

1.66

University of Ghent/Euras 2005

Folsomia candida

reproduction

384

576

1152

2.00

University of Ghent/Euras 2005

Folsomia candida

reproduction

662

993

1986

3.32

University of Ghent/Euras 2005

Folsomia candida

reproduction

828

1242

2484

3.01

University of Ghent/Euras 2005

Folsomia candida

reproduction

1100

1650

3300

3.32

University of Ghent/Euras 2005

Folsomia candida

reproduction

61.7

92.55

185.1

3.32

University of Ghent/Euras 2005

Folsomia candida

reproduction

562

843

1686

3.66

University of Ghent/Euras 2005

Folsomia candida

reproduction

320

560

476

1.25

Lock & Janssen 2002

 

 

 

 

 

 

 

Folsomia candida

mortality

 

1000

1000

1.25

Lock & Janssen 2002

 

 

 

 

 

 

 

Folsomia fimetaria

reproduction

173

259.5

519

1.12

Scott-Fordsmand et al. 1998

 

 

 

 

 

 

 

Eisenia fetida

reproduction

49.8

74.7

149.4

1.01

University of Ghent/Euras 2005

Eisenia fetida

reproduction

1110

1665

3330

1.02

University of Ghent/Euras 2005

Eisenia fetida

reproduction

54.5

81.75

163.5

1.02

University of Ghent/Euras 2005

Eisenia fetida

reproduction

362

543

1086

1.02

University of Ghent/Euras 2005

Eisenia fetida

reproduction

46.5

69.75

139.5

1.03

University of Ghent/Euras 2005

Eisenia fetida

reproduction

182

273

546

1.07

University of Ghent/Euras 2005

Eisenia fetida

reproduction

230

345

690

1.14

University of Ghent/Euras 2005

Eisenia fetida

reproduction

66.1

99.15

198.3

1.14

University of Ghent/Euras 2005

Eisenia fetida

reproduction

151

226.5

453

1.28

University of Ghent/Euras 2005

Eisenia fetida

reproduction

172

258

516

1.66

University of Ghent/Euras 2005

Eisenia fetida

reproduction

297

445.5

891

2.00

University of Ghent/Euras 2005

Eisenia fetida

reproduction

233

349.5

699

3.32

University of Ghent/Euras 2005

Eisenia fetida

reproduction

239

358.5

717

3.01

University of Ghent/Euras 2005

Eisenia fetida

reproduction

490

735

1470

3.32

University of Ghent/Euras 2005

Eisenia fetida

reproduction

186

279

558

3.32

University of Ghent/Euras 2005

Eisenia fetida

reproduction

198

297

594

3.66

University of Ghent/Euras 2005

Eisenia fetida

reproduction

180

320

362

1.25

Lock & Janssen 2002

 

 

 

 

 

 

 

Eisenia fetida

mortality

 

1000

1000

1.25

Lock & Janssen 2002

 

 

 

 

 

 

 

Enchytraeus albidus

reproduction

180

320

275

1.25

Lock & Janssen 2002

 

 

 

 

 

 

 

Enchytraeus albidus

mortality

 

127.5

510

1.25

Lock & Janssen 2002

 

 

 

 

 

 

 

Eisenia veneta

reproduction

85

300

300

1.12

Scott-Fordsmand et al. 1998

 

 

 

 

 

 

 

Lumbricus rubellus

mortality

842

1080

1190

2.52

Ma 1982

 

 

 

 

 

 

 

Microbial process

nitrification

170

255

510

1.02

University of Leuven 2005

Microbial process

nitrification

111

166.5

333

1.02

University of Leuven 2005

Microbial process

nitrification

44

66

132

1.14

University of Leuven 2005

Microbial process

nitrification

137

205.5

411

1.14

University of Leuven 2005

Microbial process

nitrification

67

100.5

201

1.66

University of Leuven 2005

Microbial process

nitrification

214

321

642

2.00

University of Leuven 2005

Microbial process

nitrification

439

658.5

1317

3.01

University of Leuven 2005

Microbial process

nitrification

169

253.5

507

3.32

University of Leuven 2005

Microbial process

nitrification

53

79.5

159

3.32

University of Leuven 2005

Microbial process

nitrification

67

100.5

201

3.66

University of Leuven 2005

 

 

 

 

 

 

 

Microbial process

N-mineralisation

257

385.5

771

2.00

Smolders 2000

Microbial process

N-mineralisation

20

30

60

2.00

Smolders 2000

 

 

 

 

 

 

 

Microbial process

Glucose respiration

22

33

66

1.02

University of Leuven 2005

Microbial process

Glucose respiration

254

381

762

1.14

University of Leuven 2005

Microbial process

Glucose respiration

376

564

1128

1.28

University of Leuven 2005

Microbial process

Glucose respiration

45

67.5

135

1.66

University of Leuven 2005

Microbial process

Glucose respiration

242

363

726

2.00

University of Leuven 2005

Microbial process

Glucose respiration

116

174

348

3.32

University of Leuven 2005

Microbial process

Glucose respiration

302

453

906

3.01

University of Leuven 2005

Microbial process

Glucose respiration

167

250.5

501

3.32

University of Leuven 2005

Microbial process

Glucose respiration

140

210

420

3.32

University of Leuven 2005

Microbial process

Glucose respiration

56

84

168

3.66

University of Leuven 2005

 

 

 

 

 

 

 

Microbial process

MRR

42

63

126

1.01

University of Leuven 2005

Microbial process

MRR

343

514.5

1029

1.02

University of Leuven 2005

Microbial process

MRR

55

82.5

165

1.14

University of Leuven 2005

Microbial process

MRR

121

181.5

363

1.28

University of Leuven 2005

Microbial process

MRR

88

132

264

2.00

University of Leuven 2005

Microbial process

MRR

203

304.5

609

3.01

University of Leuven 2005

Microbial process

MRR

446

669

1338

3.32

University of Leuven 2005

Microbial process

MRR

370

555

1110

3.66

University of Leuven 2005

 

 

 

 

 

 

 

Aspergillus flavipes

 hyphal growth

347

386.9

414.2

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Aspergillus flavus

 hyphal growth

393

510.2

600.8

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Aspergillus clavatus

 hyphal growth

13

40

79.3

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Aspergillus niger

 hyphal growth

400

474.5

527.8

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Penicillium vermiculatum

 hyphal growth

102

235.9

400.4

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Rhizopus stolonifer

 hyphal growth

288

352.2

399.8

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Trichoderma viride

 hyphal growth

530

597.9

644.8

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Gliocladium sp.

 hyphal growth

200

505

902.4

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Serratia marcescens

 colony count

155

293.3

344.1

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Proteus vulgaris

 colony count

15

77.4

216.6

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Bacillus cereus

 colony count

285

880.4

1706

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Nocardia rhodochrous

 colony count

177

577.2

821.6

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Rhodotorula rubra

 colony count

247

729.3

1565

1.05

Babich & Stotzky 1982

 

 

 

 

 

 

 

Microbial process

Respiration

400

8000

8000

2.00

Doelman & Haanstra 1984

Microbial process

Respiration

 

8000

8000

2.00

Doelman & Haanstra 1984

Microbial process

Respiration

2542

8000

8000

1.25

Doelman & Haanstra 1984

Microbial process

Respiration

 

1370

7292

1.25

Doelman & Haanstra 1984

Microbial process

Respiration

291

8000

8000

3.66

Doelman & Haanstra, 1984

Microbial process

Respiration

 

8000

8000

3.66

Doelman & Haanstra 1984

Microbial process

Respiration

 

8000

8000

3.01

Doelman & Haanstra 1984

Microbial process

Respiration

 

8000

8000

3.01

Doelman & Haanstra 1984

Microbial process

Respiration

 

3585

12 072

1.03

Doelman & Haanstra 1984

Microbial process

Respiration

27

93.9

1655

1.08

Saviozzi et al. 1997

 

 

 

 

 

 

 

Microbial process

Glutamate respiration

55

400

800

2.00

Haanstra & Doelman 1984

Microbial process

Glutamate respiration

55

400

800

1.03

Haanstra & Doelman 1984

Microbial process

Glutamate respiration

55

400

800

3.01

Haanstra & Doelman 1984

Microbial process

Glutamate respiration

 

55

110

3.66

Haanstra & Doelman 1984

 

 

 

 

 

 

 

Enzyme

ATP content

77

115.5

400

1.25

Wilke 1988

 

 

 

 

 

 

 

Enzyme activity

urease

120

180

410

2.00

Doelman & Haanstra 1986

Enzyme activity

urease

 

 

 

2.00

Doelman & Haanstra 1986

Enzyme activity

urease

2300

3450

2790

1.25

Doelman & Haanstra 1986

Enzyme activity

urease

 

 

 

1.25

Doelman & Haanstra 1986

Enzyme activity

urease

130

195

1740

3.66

Doelman & Haanstra 1986

Enzyme activity

urease

 

 

 

3.66

Doelman & Haanstra 1986

Enzyme activity

urease

90

135

370

3.01

Doelman & Haanstra 1986

Enzyme activity

urease

 

 

 

3.01

Doelman & Haanstra 1986

Enzyme activity

urease

540

810

2320

1.03

Doelman & Haanstra 1986

Enzyme activity

urease

 

 

 

1.03

Doelman & Haanstra 1986

 

 

 

 

 

 

 

Enzyme activity

phosphatase

7021

10531.5

10071

2.00

Doelman & Haanstra 1989

Enzyme activity

phosphatase

251

376.5

8040

1.25

Doelman & Haanstra 1989

Enzyme activity

phosphatase

380

570

2130

3.66

Doelman & Haanstra 1989

Enzyme activity

phosphatase

 

 

6514

3.01

Doelman & Haanstra 1989

 

 

 

 

 

 

 

Enzyme activity

arylsulfatase

372

558

2119

2.00

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

 

 

98.6

2.00

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

610

915

2347

1.25

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

2207

3310.5

5399

3.66

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

 

 

92.1

3.66

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

272

408

5658

3.01

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

 

 

2436

3.01

Haanstra & Doelman 1991

Enzyme activity

arylsulfatase

7080

10620

8099

1.03

Haanstra & Doelman 1991

 

 

 

 

 

 

 

Enzyme activity

dehydrogenase

7.9

24.3

100

2.03

Welp 1999

 

 

 

 

 

 

 

Enzyme activity

saccharase

77

115.5

400

1.25

Wilke 1988

 

 

 

 

 

 

 

Enzyme activity

protease

77

115.5

400

1.25

Wilke 1988

MRR = maize residue respiration.


Table I1:The raw toxicity data for trivalent chromium that was used in the derivation of the soil quality guidelines derived in this project, and the source of the toxicity data.

Species

Endpoint

NOEC or EC10 added

LOEC or EC30 added

EC50 added

Reference

Agrostis tenuis

growth

3333

5000

10000

Beeze 1973

 

 

 

 

 

 

Avena sativa

growth

400

600

1200

De Haan et al. 1985

Avena sativa

growth

200

300

600

De Haan et al. 1985

Avena sativa

growth

200

300

600

De Haan et al. 1985

Avena sativa

growth

400

600

1200

De Haan et al. 1985

Avena sativa

growth

200

300

600

De Haan et al. 1985

Avena sativa

growth

800

1200

2400

De Haan et al. 1985

Avena sativa

growth

500

750

1500

McGrath 1982

 

 

 

 

 

 

Beans

growth

200

500

600

Sykes et al. 1981

 

 

 

 

 

 

Brassica juncea

biomass

500

750

1100

Han et al. 2004

 

 

 

 

 

 

Grass

growth

200

500

600

Sykes et al. 1981

Grass

growth

 

 

 

 

 

 

 

 

 

 

H. vulgare

growth

200

300

600

Patterson 1971

H. vulgare

growth

200

300

600

Patterson 1971

H. vulgare

growth

200

300

600

Patterson 1971

 

 

 

 

 

 

L. sativa

growth

500

750

1500

Sykes et al. 1981

L. sativa

growth

133

200

400

Sykes et al. 1981

 

 

 

 

 

 

Lollium perenne

growth

3333

5000

10000

Beeze 1973

 

 

 

 

 

 

Phaseoleus vulgaris

growth

50

100

200.0

Wallace et al. 1976

Phaseoleus vulgaris

growth

33.3

50

100

Wallace et al. 1976

 

 

 

 

 

 

R. sativus

growth

500

750

1500

Sykes et al. 1981

R. sativus

growth

133

200

400

Sykes et al. 1981

 

 

 

 

 

 

Secale cereale

growth

233

350

700

Cunningham et al. 1975

Secale cereale

growth

233

350

700

Cunningham et al, 1975

 

 

 

 

 

 

Z. mays

growth

233

350

700

Cunningham et al. 1975

Z. mays

growth

80

320

640

Mortveldt & Giordano 1975

Z. mays

growth

1360

2040

4080

Mortveldt & Giordano 1975

 

 

 

 

 

 

E. andrei

reproduction

167

250

500.0

Molnar et al. 1989

E. andrei

reproduction

32

100

200

van Gestel et al. 1993

 

 

 

 

 

 

E. andrei

growth

320

1000

2000

van Gestel et al. 1992

 

 

 

 

 

 

E. andrei

juveniles per adult

32

100

200

van Gestel et al. 1992

 

 

 

 

 

 

E. andrei

fertility

320

1000

2000

van Gestel et al. 1992

 

 

 

 

 

 

E. andrei

fecundity

320

1000

2000

van Gestel et al. 1992

 

 

 

 

 

 

E. fetida

survival

589

883

1767

Sivakumar & Subbhuraam 2005

E. fetida

survival

552

828

1657

Sivakumar & Subbhuraam 2005

E. fetida

survival

598

897

1793

Sivakumar & Subbhuraam 2005

E. fetida

survival

609

914

1828

Sivakumar & Subbhuraam 2005

E. fetida

survival

619

928

1856

Sivakumar & Subbhuraam 2005

E. fetida

survival

567

851

1702

Sivakumar & Subbhuraam 2005

E. fetida

survival

630

946

1891

Sivakumar & Subbhuraam 2005

E. fetida

survival

549

823

1646

Sivakumar & Subbhuraam 2005

E. fetida

survival

587

880

1761

Sivakumar & Subbhuraam 2005

E. fetida

survival

585

878

1756

Sivakumar & Subbhuraam 2005

 

 

 

 

 

 

microbial process

arylsulfatase

87

130

260

Al-khafaji & Tabatabai 1979

microbial process

arylsulfatase

867

1300

2600

Al-khafaji & Tabatabai 1979

microbial process

arylsulfatase

37

55

56

Haanstra & Doelman 1991

microbial process

arylsulfatase

37

55

203

Haanstra & Doelman 1991

microbial process

arylsulfatase

55

83

235

Haanstra & Doelman 1991

microbial process

arylsulfatase

37

55

87

Haanstra & Doelman 1991

microbial process

arylsulfatase

1819

2729

2205

Haanstra & Doelman,1991

 

 

 

 

 

 

microbial process

catalase

0.11

0.67

2.08

Stępniewska et al. 2009

microbial process

catalase

0.19

0.95

2.67

Stępniewska et al. 2009

microbial process

catalase

0.18

0.798

2.03

Stępniewska et al. 2009

microbial process

catalase

0.04

0.219

0.644

Stępniewska et al. 2009

microbial process

catalase

0.72

2.33

4.88

Stępniewska et al. 2009

microbial process

catalase

0.43

1.79

4.4

Stępniewska et al. 2009

 

 

 

 

 

 

microbial process

glutamic acid decomposition

55

400

800

Haanstra & Doelman 1984

microbial process

glutamic acid decomposition

55

400

800

Haanstra & Doelman 1984

 

 

 

 

 

 

microbial process

N-mineralisation

50

200

500

Skujins et al. 1986

microbial process

N-mineralisation

4.28

18.8

47.8

Chang & Broadbent,1982

microbial process

N-mineralisation

400

600

1200

Doelman & Haanstra 1983

microbial process

N-mineralisation

423

634

1268

Doelman & Haanstra 1983

microbial process

N-mineralisation

324

486

972

Doelman & Haanstra 1983

microbial process

N-mineralisation

123

184

368

Doelman & Haanstra 1983

microbial process

N-mineralisation

8.00

12

24

Doelman & Haanstra 1983

microbial process

N-mineralisation

296

444

888

Doelman & Haanstra 1983

microbial process

N-mineralisation

431

646

1292

Doelman & Haanstra 1983

microbial process

N-mineralisation

1853

2780

5560

Doelman & Haanstra 1983

microbial process

N-mineralisation

2823

4234

8468

Doelman & Haanstra 1983

microbial process

N-mineralisation

86.7

130

260

Fu & Tabatabai 1989

microbial process

N-mineralisation

173

260

520

Liang & Tabatabai 1977

 

 

 

 

 

 

microbial process

nitrogenase

<<50

<<50

<<50

Skujins et al. 1986

 

 

 

 

 

 

microbial process

respiration

50.0

200

500

Skujins et al. 1986

microbial process

respiration

33.3

50

100

Chang & Broadbent 1981

microbial process

respiration

32.1

219

730

Doelman & Haanstra 1984

microbial process

respiration

2099

7514

>8000

Doelman & Haanstra 1984

microbial process

respiration

66.7

100

200

Ross et al. 1981

microbial process

respiration

66.7

100

200

Ross et al. 1981

microbial process

respiration

0.3

5.3

10.6

Stadelmann & Santschi-Fuhriman 1987

microbial process

respiration

21.3

32

64

Stadelmann & Santschi-Fuhriman 1987

 

 

 

 

 

 

microbial process

urease

50

200

1000.0

Skujins et al. 1986

microbial process

urease

0.093

0.25

0.4

Samborska et al. 2004

microbial process

urease

50

75

150

Bremner & Douglas 1971

microbial process

urease

390

585

630

Doelman & Haanstra, 1986

microbial process

urease

890

1335

1110

Doelman & Haanstra 1986

microbial process

urease

350

525

420

Doelman & Haanstra 1986

microbial process

urease

369

554

1360

Doelman & Haanstra 1986

microbial process

urease

173

260

520

Tabatabai 1977

microbial process

urease

26

26

52

Tabatabai 1977

14             Glossary

ACL (EC50) is the added contaminant limit calculated using 50% effect concentration (EC50) toxicity data.

ACL (LOEC & EC30) is the added contaminant limit calculated using lowest observed effect concentration (LOEC) and 30% effect concentration (EC30) toxicity data.

ACL (NOEC & EC10) is the added contaminant limit calculated using no observed effect concentration (NOEC) and 10% effect concentration (EC10) toxicity data.

Adaptation is (1) change in an organism, in response to changing conditions of the environment (specifically chemical), which occurs without any irreversible disruption of the given biological system and without exceeding the normal (homeostatic) capacities of its response, and (2)  a process by which an organism stabilises its physiological condition after an environmental change.

Added contaminant limit (ACL) is the added concentration of a contaminant above which further appropriate investigation and evaluation of the impact on ecological values will be required. ACL values are generated in the process of deriving the three sets of SQGs (calculated using NOEC and EC10, LOEC and EC30, and EC50 toxicity data). ACL values denote which toxicity data was used in their derivation by using subscripts. Thus, ACL(NOEC &EC10), ACL(LOEC & EC30) and ACL(EC50) are calculated using NOEC & EC10, LOEC & EC30, and EC50 data respectively.

Adsorption is the adhesion of molecules to surfaces of solids.

Ambient background concentration (ABC) of a contaminant is the soil concentration in a specified locality that is the sum of the naturally occurring background and the contaminant levels that have been introduced from diffuse or non-point sources by general anthropogenic activity not attributed to industrial, commercial, or agricultural activities.

An area of ecological significance is one where the planning provisions or land-use designation is for the primary intention of conserving and protecting the natural environment. This would include national parks, state parks, and wilderness areas and designated conservation areas.

Bioaccumulation factor (BAF) is a partition coefficient for the distribution of a chemical between an organism exposed through all possible routes and an environmental compartment or food.

Bioaccumulation is the net result of the uptake, distribution and elimination of a substance due to all routes of exposure; that is, exposure to air, water, soil/sediment and food.

Bioavailability is the ability of substances to interact with the biological system of an organism. Systemic bioavailability will depend on the chemical or physical reactivity of the substance and its ability to be absorbed through the gastrointestinal tract, respiratory tract or skin. It may be locally bioavailable at all these sites.

Bioconcentration factor (BCF)  is a quantitative measure of a chemical’s tendency to be taken up from the ambient environment (for example, water for aquatic organisms and soil or soil pore water for soil organisms). The BCF is the ratio of the concentration of the chemical in tissue (or a specific organ) and the concentration in the ambient environment.

Bioconcentration is the net result of the uptake, distribution and elimination of a substance due to exposure in the ambient environment (for example, water for aquatic organisms and soil or soil pore water for soil organisms).

Biological half life is the time needed to reduce the concentration of a test chemical in the environmental compartment or organisms to half the initial concentration, by transport processes, (for example, diffusive elimination), transformation processes (for example, biodegradation or metabolism) or growth.

Biomagnification factor (BMF) is a quantitative measure of a chemical’s tendency to be taken up through the food web.

Biomagnification is the accumulation and transfer of chemicals via the food web due to ingestion, resulting in an increase of the internal concentration in organisms at the succeeding trophic levels.

Chronic is extended or long-term exposure to a stressor, conventionally taken to include at least a tenth of the life-span of a species.

Default conversion factors are numerical values that are used to convert a measure of toxicity to another measure of toxicity (for example, EC50 to a NOEC) when no experimentally determined values are available.

Ecological investigation level (EIL) is the concentration of a contaminant above which further appropriate investigation and evaluation of the impact on ecological values will be required. The EILs are calculated using EC30 or LOEC toxicity data. EILs are the sum of the added contaminant limit (ACL) and the ambient background concentration (ABC) and the level is expressed in terms of total concentration.

ECx  is effective concentration; the concentration which affects X% of a test population after a specified exposure time.

Environmental fate is the destiny of a chemical or biological pollutant after release into the natural environment.

Generic soil quality guidelines describe a single concentration-based value that applies to all Australian soils that have a particular land use. These are derived when normalisation relationships are not available. Compare these with soil-specific soil quality guidelines.

Kd (see watersoil partition coefficient).

Koc (see organic carbonwater partition coefficient).

Kow (see octanolwater partition coefficient).

Leaching is the dissolving of contaminants in soil and subsequent downward transport to groundwater or surface water bodies.

Leachate is water that has percolated through a column of soil.

LOEC is the lowest observed effect concentration; the lowest concentration of a material used in a test that has a statistically significant effect on the exposed population of test organisms compared to the control.

NOEC is no observed effect concentration; the highest concentration of a test substance to which organisms are exposed that does not cause any observed and statistically significant adverse effects on the organisms compared to the controls.

Normalisation relationships are empirical, generally linear, relationships that can predict the toxicity of a contaminant to an organism using soil physicochemical properties. These are used in the EIL derivation methodology to generate soil-specific soil quality guidelines.

Octanolwater partitioning (Kow) is the ratio of a chemical’s solubility in n-octanol and water at equilibrium. This is widely used as a surrogate for the ability of a contaminant to accumulate in organisms and to biomagnify. These are often expressed in the logarithmic form (that is, log Kow). Chemicals with a log Kow value ≥4 is considered to have the potential to biomagnify.  There is a linear relationship between log Kow and log Koc values. Thus, Kow can also be used to indicate the ability of chemical to leach to groundwater. A log Kow value <2 indicates a chemical has the potential to leach to groundwater.

Organic carbonwater partition coefficient (Koc) is the ratio of a chemical’s solubility in organic carbon and water at equilibrium. This is widely used as a surrogate for the ability of a contaminant to accumulate in soils and conversely to leach to groundwater or to be removed by surface run-off. These are often expressed in the logarithmic form (that is, log Koc). Chemicals with a log Koc <2.4 were considered to be mobile and therefore have the ability in some soils to leach to groundwater.

Precautionary principle is the general principle by which all that can reasonably be expected is done to prevent unnecessary risks.

Reference site is a relatively unpolluted site used for comparison with polluted sites in environmental monitoring studies or used for the assessment of ambient background concentrations of contaminants.

Soil quality guidelines (SQGs) are any concentration-based limits for contaminants in soils. Ecological investigation levels are a type of SQG.

Soil-specific soil quality guidelines is a suite of concentration-based values, where each value applies to a soil with different physicochemical properties. These values take into account properties of soils that modify the bioavailability and toxicity of contaminants. These can only be derived if normalisation relationships are available. Compare these to generic SQGs.

Speciation is the exact chemical form of contaminant in which an element occurs in a sample.

Statistically significant effects are effects (responses) in the exposed population which are different from those in the controls at a statistical probability level of p <0.05.

 

Steady state is the non-equilibrium state of a system in which matter flows in and out at equal rates so that all of the components remain at constant concentrations (dynamic equilibrium).

Watersoil partition coefficient (Kd) is the ratio of the concentration of a contaminant in soil pore water to that in the solid phase of soil at equilibrium. The units are L/kg. This contaminant property is affected by physicochemical properties of the contaminant and the soil.  This property is usually expressed as a logarithm (that is, log Kd). A chemical with log Kd <3 is considered to have the potential to leach.

 

15             Shortened forms

ABC

ambient background concentration

ACL

added contaminant limit

AF

assessment factor

ALF

ageing and leaching factor

ANZECC

Australia and New Zealand Environment and Conservation Council

ARMCANZ

Agriculture and Resource Management Council of Australia and New Zealand

BAF

bioaccumulation factor

BCF

bioconcentration factor

BMF

biomagnification factor

CCME

Canadian Council of Ministers of the Environment

CEC

cation exchange capacity

DAF

dilution and attenuation factor

EC

European cCommission

EC10

10% effect concentration

EC30

30% effect concentration

EC50

50% effect concentration

Eco-SSL

ecological soil screening level

EIL

ecological investigation level

ERA

ecological risk assessment

EQG

environmental quality guideline

EU

European Union

HIL

health-based investigation level

LD10

The dose that is lethal to 10% of organisms

LC10

The concentration that is lethal to 10% of organisms

LOEC

lowest observed effect concentration

MATC

maximum acceptable toxicant concentration

MRM

maize residue mineralisation

NA

not available

N/A

not applicable

NBRP

National Biosolids Research Program

NEPC

National Environment Protection Council

NEPM

National Environment Protection Measure

NOEC

no observed effect concentration

NS

Not statistically significant (P>0.05)

OC

organic carbon

OECD

Organisation for Economic Cooperation and Development

PNEC

predicted no-effect concentration

PNR

potential nitrification rate

SIN

substrate induced nitrification

SIR

substrate induced respiration

SQG

soil quality guideline

SSD

species sensitivity distribution

US EPA

United States Environmental Protection Agency

TRV

toxicity reference value

TV

trigger value

VROM

Ministry of Housing, Spatial Planning, and the Environment (The Netherlands)

 


[1] The soil-specific Zn ACLs for commercial/industrial land use are provided in Appendix B, Table 1.

[2] Soil pore water is the predominant source of groundwater. As the soil pore water leaches it passes through material that can bind the contaminants (attenuation), thus reducing their concentration. Also, in the majority of cases groundwater catchments will contain both contaminated and uncontaminated soils; pore water from the contaminated soil will be diluted by that from the uncontaminated (dilution). Therefore a a dilution and attenuation factor (DAF) is used to convert soil pore water concentrations to groundwater concentrations. The fraction of contaminated land to the total area of the groundwater/aquifer catchment can be used to calculate the DAF as indicated below:

DAF = 100 ÷ percentage of contaminated soil in catchment  

[3] A = the standard residential setting with garden/accessible soils and home-grown produce contributing <10% of vegetable and fruit intake. B = residential with minimal opportunities for soil access: includes dwellings with fully and permanently paved yard space such as high rise apartments and flats. C = parks, recreational open space and playing fields: includes secondary schools. D = Commercial/industrial: includes premises such as shops and offices as well as factories and industrial sites.

[4] For cations with a single ALF, these were used to calculate the mean ALF. For cations with a range of values, both the lowest and highest values were used to calculate the mean. Therefore the value of 2.35 was the mean of 3, 2, 1, 1, 3, 1.1, 3.5, 4.2, 1.