Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Ecotoxicological information

Toxicity to terrestrial plants

Currently viewing:

Administrative data

Link to relevant study record(s)

Referenceopen allclose all

Endpoint:
toxicity to terrestrial plants: long-term
Type of information:
experimental study
Adequacy of study:
key study
Study period:
The study was conducted between 22 May 2010 and 29 September 2010.
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: guideline study on Gas-to-liquids (GTL) substance covering the carbon range from C18 to C50
Qualifier:
according to guideline
Guideline:
OECD Guideline 208 (Terrestrial Plants Test: Seedling Emergence and Seedling Growth Test)
Deviations:
no
GLP compliance:
yes
Analytical monitoring:
no
Details on sampling:
Following a preliminary range-finding test, five plant species; three dicotyledonous species, soybean (Glycine max), tomato (Lycopersicon
esulentum) and mustard (Sinapis alba) and two monocotyledonous species, oat (Avena sativa) and perennial ryegrass (Lolium perenne) were
exposed to concentrations of 100, 180, 320, 560 and 1000 mg/kg. The number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily for 21 or 22 days after 50% emergence in the control for each species.

Definitive test
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 100, 180, 320, 560 and
1000 mg/kg using the test species soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and
perennial ryegrass (Lolium perenne).

Experimental preparation
For the purpose of the definitive test the test item was added directly to the soil.

In order to reduce the organic carbon content of the soil substrate the supplied soil was mixed in a 50:50 w/w ratio with sand. A total of 17 kg (dry weight) of soil substrate was required for each test concentration. This equated to 17.6 kg (wet weight) of supplied soil therefore 8.8 kg of sand was mixed with 8.8 kg of wet soil to give the final soil substrate.

Amounts of test item (850, 1530, 2720, 4760 and 8500 mg) were each separately added to 2 kg of sand in a 5 litre plastic bottle and mixed in a cement mixer for 24 hours after which 1.5 kg (wet weight) of soil was added to each bottle and mixed using a cement mixer for a further 24 hours. A further 2.4 kg of sand and 2.4 kg (wet weight) of soil was then incorporated into each pre-mix by mixing using a Hobart A200N mixer for approximately 15 minutes to give the 100, 180, 320, 560 and 1000 mg/kg test concentrations respectively. This was prepared in duplicate.
At the request of the Sponsor, four studies were to be conducted simultaneously. Due to the method of preparation used it was not possible to prepare the test concentrations for all the studies at the same time. Therefore, the prepared test concentrations were stored at approximately 4°C prior to sowing.
Prior to sowing, the 100, 180, 320, 560 and 1000 mg/kg test concentrations were further mixed, with water added to dampen the soil, using a Hobart A200N mixer for approximately 15 minutes. Due to the amount of mixing required to conduct the four studies simultaneously, following the final mixing the soil substrate for each test concentration was transferred to pots and maintained at approximately 14°C for approximately 24 hours prior to sowing.

The control was prepared, in duplicate, in an identical manner without the addition of test item.
Vehicle:
no
Details on preparation and application of test substrate:
Not Applicable
Species:
Glycine max (G. soja)
Plant group:
Dicotyledonae (dicots)
Details on test organisms:
The soybean seeds were obtained from Herbiseed, Twyford, UK and were supplied untreated. Upon arrival the seeds were stored under cool, dry conditions.
Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1 in section any other
information on materials and methods.
Species:
Lycopersicon esculentum
Plant group:
Dicotyledonae (dicots)
Details on test organisms:
The tomato seeds were obtained from Herbiseed, Twyford, UK and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions.
Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1 in section any other information on materials and methods.
Species:
Sinapis alba
Plant group:
Dicotyledonae (dicots)
Details on test organisms:
The mustard seeds were obtained from Herbiseed, Twyford, UK and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions.
Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1 in section any other information on materials and methods.
Species:
Avena sativa
Plant group:
Monocotyledonae (monocots)
Details on test organisms:
The oat seeds were obtained from Senova Ltd., Cambridge, UK and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions.
Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1 in section any other
information on materials and methods.
Species:
Lolium perenne
Plant group:
Monocotyledonae (monocots)
Details on test organisms:
The perennial ryegrass seeds were obtained from Herbiseed, Twyford, UK and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions.
Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1 in section any other information on materials and methods.
Test type:
other: Terrestrial plant test seedling emergence and seedling
Study type:
laboratory study
Substrate type:
natural soil
Limit test:
no
Total exposure duration:
22 d
Test temperature:
The temperature was maintained at 7°C to 37°C
pH:
The soil has a pH of 8
Moisture:
Not reported
Details on test conditions:
Exposure System
The exposure vessels consisted of polypropylene pots with a depth of 9.9 cm and a diameter of 13 cm. For each species, four replicates were maintained for the control and each test concentration. Each pot contained approximately 850 g (dry weight) of substrate. After planting, each pot was placed in a plant pot saucer which served as a sub-irrigation reservoir. Initial watering was via the surface to encourage germination. All subsequent watering was by sub-irrigation as required.

The study was conducted in a greenhouse equipped with artificial lighting and heating systems.

Procedure

Range-finding test
In the range-finding test three dicotyledonous species; soybean (Glycine max), tomato (Lycopersicon esculentum) and mustard (Sinapis alba) and
two monocotyledonous species; oat (Avena sativa) and perennial ryegrass (Lolium perenne) were exposed to a series of nominal test concentrations of 100 and 1000 mg/kg.

The test item was incorporated directly into the soil substrate.

In order to reduce the organic carbon content of the soil substrate the supplied soil was mixed in a 50:50 w/w ratio with sand. A total of 8.5 kg (dry weight) of soil substrate was required for each test concentration therefore 4.25 kg (dry weight) of supplied soil was required. This equated to 4.39 kg (wet weight) of supplied soil therefore 4.39 kg of sand was mixed with this to give the final soil substrate.

Amounts of test item (850 and 8500 mg) were each separately added to 2 kg of sand in a 5 litre plastic bottle and mixed in a cement mixer for 24 hours after which 1.55 kg (wet weight) of soil was added to each bottle and mixed using a cement mixer for a further 24 hours. A further 2.39 kg of sand and 2.84 kg (wet weight) of soil was then incorporated into each pre-mix by mixing using a Hobart A200N mixer for approximately 30 minutes to give the 100 and 1000 mg/kg test concentrations respectively.
At the request of the Sponsor, four studies were to be conducted simultaneously. Due to the method of preparation used it was not possible to prepare the test concentrations for all the studies at the same time. Therefore, the prepared test concentrations were stored at approximately 4°C prior to sowing.

Prior to sowing, the 100 and 1000 mg/kg test concentrations were further mixed, with water added to dampen the soil, using a Hobart A200N mixer for approximately 15 minutes.
The control was prepared in an identical manner without the addition of test item.
In the range-finding test, five seeds were placed in each test and control pot for each species. Two replicates were prepared for each concentration. Following sowing, the pots were surface irrigated to encourage germination and then placed in a randomised fashion in the greenhouse. The temperature was maintained at 9 degree C to 40 degree C with a photoperiod of approximately 16 hours light and 8 hours darkness. Some of the temperatures were observed to be outside the range given in the study plan. This deviation was considered not to affect the integrity or the outcome of the study as no morphological abnormalities were observed in the control plants.
After the initial watering the pots were watered as necessary using sub-irrigation. All the pots were monitored daily after sowing for emergence and the date when 50% emergence occurred in the control pots for each species was recorded. For 21 days following 50% emergence in the control pots the number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily in the test and control pots for each species. On Day 21 the above ground portion of each seedling was harvested and the dry weight determined by placing in pre-weighed containers and drying in an oven at approximately 60°C. For oat and perennial ryegrass the seedlings were harvested on Day 22 of the test due to Day 21 falling on a weekend. In addition, the soybean seedlings were harvested on Day 22 in error. This additional day was considered not to affect the study.
The control groups were maintained under identical conditions but not exposed to the test item. Data from the control groups were shared with similar concurrent studies.

Definitive test
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 100, 180, 320, 560 and 1000 mg/kg using the test species soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and perennial ryegrass (Lolium perenne).



Exposure conditions
At the start of the test five seeds were placed in each test and control pot at random. Four replicate pots were prepared for the control and each test concentration for each species. Following sowing, the pots were surface irrigated to encourage germination and then placed in a randomised fashion in a greenhouse. The temperature was maintained at 7 degree C to 37 degree C with a photoperiod of approximately 16 hours light and 8 hours darkness. After the initial watering the pots were watered as necessary using sub-irrigation.

The control groups were maintained under identical conditions but not exposed to the test item. Data from the control groups were shared with similar concurrent studies.

All the pots were monitored daily after sowing for emergence and the date when 50% emergence occurred in the control pots for each species was recorded. For 21 days following 50% emergence in the control pots, the number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily in the test and control pots for each species. On Day 21 the above ground portion of each seedling (except soybean) was harvested and the dry weight determined by placing in pre-weighed containers and drying in an oven at approximately 60°C. The soybean seedlings were harvested on Day 22 of the test due to Day 21 falling on a weekend. This additional day was considered not to affect the study.

Nominal and measured concentrations:
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 100, 180, 320, 560 and 1000 mg/kg using the test species soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and perennial ryegrass (Lolium perenne).
Reference substance (positive control):
no
Species:
Glycine max (G. soja)
Duration:
22 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Glycine max (G. soja)
Duration:
22 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Lycopersicon esculentum
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Lycopersicon esculentum
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Sinapis alba
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
germination
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Sinapis alba
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Avena sativa
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Avena sativa
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Lolium perenne
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Species:
Lolium perenne
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil dw
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks:
and growth based on final dry weight
Remarks on result:
other: 95 % CL Not stated
Details on results:
RESULTS
Range-finding Test
A summary of the percentage emergence and mortality for each species during the range-finding test is given in Table 2 - see in attached section.
No morphological effects were observed throughout the duration of the test.

Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the emergence and shoot dry weight data for each species.

There were no significant differences (P<0.05) between the control and all the test groups in terms of emergence for each species.
There were no significant decreases in shoot dry weight (P<0.05) between the control and all the test groups at test termination for oat, perennial ryegrass, tomato and mustard.

A significant decrease in shoot dry weight (P<0.05) was observed between the control and the 100 mg/kg test group at test termination for soybean. A review of the data indicated that this result was probably due to a single seedling which showed a greatly reduced weight compared to the remainder of the seedlings. It was therefore considered that this single value may have skewed the analysis. Given that no significant decrease in shoot dry weight was observed between the control and 1000 mg/kg test concentration, this was considered not to affect the outcome of the study.
For perennial ryegrass and mustard a significant increase in shoot dry weight was observed between the control and the 100 and 1000 mg/kg test concentrations respectively. This was considered not to affect the outcome of the test as the effect observed was not a reduction in weight.
Based on this information, test concentration of 100, 180, 320, 560 and 1000 mg/kg were selected for each species for the definitive test.

Definitive Test
Emergence Data
Soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and perennial ryegrass (Lolium perenne) reached 50% emergence in the control on Days 9, 10, 4, 5 and 7 after sowing respectively.
A summary of the percentage emergence for each species are given in Tables 3 to 7 - see in attached section

Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the emergence data for each species.

There were no significant differences (P<0.05) between the control and all the test groups in terms of emergence for each species.
Inspection of the emergence data based on the nominal test concentrations gave the following results:

Species EC50 (emergence) (mg/kg)
Soybean >1000
Tomato >1000
Mustard >1000
Oat >1000
Perennial Ryegrass >1000

The No Observed Effect Concentration for each species was 1000 mg/kg. The No Observed Effect Concentration is based upon no significant differences (P<0.05) between the test concentrations and the control.

Morphological Effects
A summary of the percentage mortality, for each species is given in Table 8 - see in attached section

No morphological abnormalities were observed for each species throughout the test.

Shoot Dry Weight Data
Shoot mean dry weight values for each species are given in Tables 9 to 13 - see in attached section.

Individual values for shoot dry weights are given in Appendix 1 - see in attached section

Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the shoot dry weight data for each species.
There was no significant decrease in shoot dry weight (P<0.05) between the control and all the test groups in terms of shoot dry weights at test termination for all test species.

A significant increase in shoot dry weight was observed at test concentrations of 180 and 320 mg/kg for perennial ryegrass and 560 and 1000 mg/kg for mustard. Given that the effect observed was not a detrimental effect, this was considered not to affect the outcome of the study.
Inspection of the shoot dry weight data based on the nominal test concentrations gave the following results:

Species EC50 (growth) (mg/kg)
Soybean >1000
Tomato >1000
Mustard >1000
Oat >1000
Perennial Ryegrass >1000

The No Observed Effect Concentration for each species was 1000 mg/kg. The No Observed Effect Concentration is based upon no significant differences (P<0.05) between the test concentrations and the control.

Physico-chemical measurements
The temperature was maintained at 7 degree C to 37 degree C and the relative humidity at 20% to 89% with a photoperiod of approximately 16 hours light and 8 hours darkness.

Some of the temperatures were observed to be outside the range given in the study plan. This deviation was considered not to affect the integrity or the outcome of the study as no morphological abnormalities were observed in the control plants.

CONCLUSION
The EC50 (emergence) and EC50 (growth based on final dry weight) for the test item based on nominal test concentrations for the five species tested were as follows:
Species EC50 (emergence) (mg/kg) No Observed Effect Concentration (mg/kg) EC50
(growth) (mg/kg) No Observed Effect Concentration (mg/kg)
Soybean >1000 1000 >1000 1000
Tomato >1000 1000 >1000 1000
Mustard >1000 1000 >1000 1000
Oat >1000 1000 >1000 1000
Perennial Ryegrass >1000 1000 >1000 1000
Reported statistics and error estimates:
Statistical analysis of the emergence and dry weight data for each species was performed using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955). All statistical analyses were performed using the SAS computer software package (SAS 1999 - 2001).

Due to the nature and quantity of the tables, all tables have been attached (see "Attached background material").

Validity criteria fulfilled:
yes
Conclusions:
The EC50 (emergence) and EC50 (growth based on final dry weight) for the test item based on nominal test concentrations for the five species tested were as follows:

Species EC50 (emergence)(mg/kg) NOEC (mg/kg) EC50 (growth) mg/kg) NOEC (mg/kg)

Soybean >1000 1000 >1000 1000
Tomato >1000 1000 >1000 1000
Mustard >1000 1000 >1000 1000
Oat >1000 1000 >1000 1000
Perennial Ryegrass >1000 1000 >1000 1000


Executive summary:

Introduction.

A study was performed to assess the effects of the test item on the emergence and growth of five plant species. The method followed that described in the OECD Guidelines for the Testing of Chemicals: Guideline 208: Terrestrial (Non-target) Plant Test: Seedling Emergence and Seedling Growth Test (July 2006).

Methods.

Following a preliminary range-finding test, five plant species; three dicotyledonous species, soybean (Glycine max), tomato (Lycopersicon esulentum) and mustard (Sinapis alba) and two monocotyledonous species, oat (Avena sativa) and perennial ryegrass (Lolium perenne) were exposed to concentrations of 100, 180, 320, 560 and 1000 mg/kg. The number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily for 21 or 22 days after 50% emergence in the control for each species.

Results.

The EC50(emergence) and EC50(growth based on final dry weight) for the test item based on nominal test concentrations for the five species tested were as follows:

Species

EC50(emergence) (mg/kg)

No Observed Effect Concentration (mg/kg)

EC50

(growth) (mg/kg)

No Observed Effect Concentration (mg/kg)[1]

Soybean

>1000

1000

>1000

1000

Tomato

>1000

1000

>1000

1000

Mustard

>1000

1000

>1000

1000

Oat

>1000

1000

>1000

1000

Perennial Ryegrass

>1000

1000

>1000

1000


[*]No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control and no morphological abnormalities were observed

Endpoint:
toxicity to terrestrial plants: long-term
Type of information:
experimental study
Adequacy of study:
key study
Study period:
The study was conducted between 29 May 2010 and 29 September 2010.
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: guideline study on Gas-to-liquids (GTL) substance covering the carbon range from C8 to C26
Qualifier:
according to guideline
Guideline:
OECD Guideline 208 (Terrestrial Plants Test: Seedling Emergence and Seedling Growth Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Analytical monitoring:
no
Details on sampling:
For the purpose of the definitive test the test item was added directly to the soil.

Range-finding test concentrations were:
100 and 1000 mg/kg. The test item was incorporated directly into the soil substrate.


For the definitive test
100, 180, 320, 560 and 1000 mg/kg test concentrations respectively. The test item was incorporated directly into the soil substrate.

The prepared test concentrations were stored at approximately 4°C prior to sowing.
Vehicle:
no
Details on preparation and application of test substrate:
Range-finding test
Amounts of test item (850 and 8500 mg) were each separately added to 2 kg of sand in a 5 litre plastic bottle and mixed in a cement mixer for 24 hours after which 1.55 kg (wet weight) of soil was added to each bottle and mixed using a cement mixer for a further 24 hours. A further 2.39 kg of sand and 2.84 kg (wet weight) of soil was then incorporated into each pre-mix by mixing using a Hobart A200N mixer for approximately 30 minutes to give the 100 and 1000 mg/kg test concentrations respectively.


Definitive test
For the purpose of the definitive test the test item was added directly to the soil.
Amounts of test item (850, 1530, 2720, 4760 and 8500 mg) were each separately added to 2 kg of sand in a 5 litre plastic bottle and mixed in a cement mixer for 24 hours after which 1.5 kg (wet weight) of soil was added to each bottle and mixed using a cement mixer for a further 24 hours. A further 2.4 kg of sand and 2.9 kg (wet weight) of soil was then incorporated into each pre-mix by mixing using a Hobart A200N mixer for approximately 15 minutes to give the 100, 180, 320, 560 and 1000 mg/kg test concentrations respectively. These were prepared in duplicate.

At the request of the Sponsor, four studies were to be conducted simultaneously. Due to the method of preparation used it was not possible to prepare the test concentrations for all the studies at the same time. Therefore, the prepared test concentrations were stored at approximately 4°C prior to sowing.
Prior to sowing, the 100, 180, 320, 560 and 1000 mg/kg test concentrations were further mixed, with water added to dampen the soil, using a Hobart A200N mixer for approximately 15 minutes. Due to the amount of mixing required to conduct the four studies simultaneously, following the final mixing the soil substrate for each test concentration was transferred to pots and maintained at approximately 14°C for approximately 24 hours prior to sowing.
The control was prepared, in duplicate, in an identical manner without the addition of test item.
Species:
Lycopersicon esculentum
Plant group:
Dicotyledonae (dicots)
Details on test organisms:
The seeds were supplied by a reputable UK supplier (for full details please see full study report) and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions. Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1.
Species:
Sinapis alba
Plant group:
Dicotyledonae (dicots)
Details on test organisms:
The seeds were supplied by a reputable UK supplier (for full details please see full study report) and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions. Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1.
Species:
Avena sativa
Plant group:
Monocotyledonae (monocots)
Details on test organisms:
The seeds were supplied by a reputable UK supplier (for full details please see full study report) and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions. Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1.
Species:
Lolium perenne
Plant group:
Monocotyledonae (monocots)
Details on test organisms:
The seeds were supplied by a reputable UK supplier (for full details please see full study report) and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions. Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1.
Species:
Glycine max (G. soja)
Plant group:
Dicotyledonae (dicots)
Details on test organisms:
The seeds were supplied by a reputable UK supplier (for full details please see full study report) and were supplied untreated.
Upon arrival the seeds were stored under cool, dry conditions. Details of seed variety, lot number, date received, planting depth and germination percentages are given in Table 1.
Test type:
other: SEEDLING EMERGENCE AND SEEDLING GROWTH TEST
Study type:
laboratory study
Substrate type:
natural soil
Limit test:
no
Total exposure duration:
21 d
Remarks:
On Day 21 the above ground portion of each seedling (except soybean) was harvested. The soybean seedlings were harvested on Day 22 of the test due to Day 21 falling on a weekend. This additional day was considered not to affect the study.
Post exposure observation period:
Not applicable
Test temperature:
The temperature was maintained at 7 °C to 37 °C
pH:
The soil was characterised by a reputable Laboratory (for full details please see full study report) as having a pH of 8.0
Moisture:
After planting, each pot was placed in a plant saucer which served as a sub-irrigation reservoir. Initial watering was via the surface to encourage germination. All subsequent watering was by sub-irrigation as required.
Details on test conditions:
Soil
The soil was supplied by Sporting Surface Supplies Ltd, Reigate, Surrey, UK. The soil was characterised by NRM Laboratories as a sandy loam with 3.8% organic matter content and a pH of 8.0. The organic matter content of the soil was in excess of the 1% to 3% given in the study plan. Therefore the soil was mixed 50:50 w/w with sand prior to use to give a nominal organic carbon content of 1.5% (equivalent to 3% organic matter).

Exposure System
The exposure vessels consisted of polypropylene pots with a depth of 9.9 cm and a diameter of 13 cm. For each species, four replicates were maintained for the control and each test concentration. Each pot contained approximately 850 g (dry weight) of substrate. After planting, each pot was placed in a plant saucer which served as a sub-irrigation reservoir. Initial watering was via the surface to encourage germination. All subsequent watering was by sub-irrigation as required.
The study was conducted in a greenhouse equipped with artificial lighting and heating systems.

Procedure
Range-finding test
In the range-finding test three dicotyledonous species; soybean (Glycine max), tomato (Lycopersicon esculentum) and mustard (Sinapis alba) and two monocotyledonous species; oat (Avena sativa) and perennial ryegrass (Lolium perenne) were exposed to a series of nominal test concentrations of 100 and 1000 mg/kg. The test item was incorporated directly into the soil substrate.
In order to reduce the organic carbon content of the soil substrate the supplied soil was mixed in a 50:50 w/w ratio with sand. A total of 8.5 kg (dry weight) of soil substrate was required for each test concentration therefore 4.25 kg (dry weight) of supplied soil was required. This equated to 4.39 kg (wet weight) of supplied soil therefore 4.39 kg of sand was mixed with this to give the final soil substrate.
Amounts of test item (850 and 8500 mg) were each separately added to 2 kg of sand in a 5 litre plastic bottle and mixed in a cement mixer for 24 hours after which 1.55 kg (wet weight) of soil was added to each bottle and mixed using a cement mixer for a further 24 hours. A further 2.39 kg of sand and 2.84 kg (wet weight) of soil was then incorporated into each pre-mix by mixing using a Hobart A200N mixer for approximately 30 minutes to give the 100 and 1000 mg/kg test concentrations respectively.
At the request of the Sponsor, four studies were to be conducted simultaneously. Due to the method of preparation used it was not possible to prepare the test concentrations for all the studies at the same time. Therefore, the prepared test concentrations were stored at approximately 4°C prior to sowing.
Prior to sowing, the 100 and 1000 mg/kg test concentrations were further mixed, with water added to dampen the soil, using a Hobart A200N mixer for approximately 15 minutes.
The control was prepared in an identical manner without the addition of test item.
In the range-finding test, five seeds were placed in each test and control pot for each species. Two replicates were prepared for each concentration. Following sowing, the pots were surface irrigated to encourage germination and then placed in a randomised fashion in the greenhouse.
The temperature was maintained at 9°C to 40°C with a photoperiod of approximately 16 hours light and 8 hours darkness. Some of the temperatures were observed to be outside the range given in the study plan. This deviation was considered not to affect the integrity or the outcome of the study as no morphological abnormalities were observed in the control plants.
After the initial watering the pots were watered as necessary using sub-irrigation. All the pots were monitored daily after sowing for emergence and the date when 50% emergence occurred in the control pots for each species was recorded. For 21 days following 50% emergence in the control pots the number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily in the test and control pots for each species. On Day 21 the above ground portion of each seedling was harvested and the dry weight determined by placing in pre-weighed containers and drying in an oven at approximately 60°C. For oat and perennial ryegrass the seedlings were harvested on Day 22 of the test due to Day 21 falling on a weekend. In addition, the soybean seedlings were harvested on Day 22 in error. This additional day was considered not to affect the study.
The control groups were maintained under identical conditions but not exposed to the test item.  Data from the control groups were shared with similar concurrent studies.
Statistical analysis of the emergence and dry weight data for each species was performed using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955).  All statistical analyses were performed using the SAS computer software package (SAS 1999 - 2001).

Definitive test
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 100, 180, 320, 560 and 1000 mg/kg using the test species soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and perennial ryegrass (Lolium perenne).

Experimental preparation
For the purpose of the definitive test the test item was added directly to the soil.
In order to reduce the organic carbon content of the soil substrate the supplied soil was mixed in a 50:50 w/w ratio with sand. A total of 17 kg (dry weight) of soil substrate was required for each test concentration. This equated to 17.6 kg (wet weight) of supplied soil therefore 8.8 kg of sand was mixed with 8.8 kg of wet soil to give the final soil substrate.

Exposure conditions
At the start of the test five seeds were placed in each test and control pot at random. Four replicate pots were prepared for the control and each test concentration for each species. Following sowing, the pots were surface irrigated to encourage germination and then placed in a randomised fashion in a greenhouse. The temperature was maintained at 7°C to 37°C with a photoperiod of approximately 16 hours light and 8 hours darkness. After the initial watering the pots were watered as necessary using sub-irrigation.
The control groups were maintained under identical conditions but not exposed to the test item. Data from the control groups were shared with similar concurrent studies.
All the pots were monitored daily after sowing for emergence and the date when 50% emergence occurred in the control pots for each species was recorded. For 21 days following 50% emergence in the control pots, the number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily in the test and control pots for each species. On Day 21 the above ground portion of each seedling (except soybean) was harvested and the dry weight determined by placing in pre-weighed containers and drying in an oven at approximately 60°C. The soybean seedlings were harvested on Day 22 of the test due to Day 21 falling on a weekend. This additional day was considered not to affect the study.

Physico-chemical measurements
Light intensity, relative humidity and temperature were recorded daily throughout the test. Light intensity was measured using a Hobo H8 data logger and the temperature and relative humidity were measured using a Testo temperature/humidity data logger.

Evaluation of data
An estimate of the EC50 (emergence) values was given by inspection of the data.
An estimate of the EC50 (growth) values was given by inspection of the data for soybean, tomato, mustard and oat.
The EC50 (growth) value and associated confidence limits for perennial ryegrass was calculated by the maximum-likelihood probit method (Finney 1971) using the ToxCalc computer software package (ToxCalc 1999).
Probit analysis is used where two or more partial responses to exposure are shown.
Statistical analysis of the emergence and dry weight data for each species was performed using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955). All statistical analyses were performed using the SAS computer software package (SAS 1999 - 2001).
Nominal and measured concentrations:
Range-finding test concentrations were:
100 and 1000 mg/kg. The test item was incorporated directly into the soil substrate.


For the definitive test
100, 180, 320, 560 and 1000 mg/kg test concentrations respectively. The test item was incorporated directly into the soil substrate.
Reference substance (positive control):
no
Species:
Lolium perenne
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL 760 - 3300
Species:
Avena sativa
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Sinapis alba
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Lycopersicon esculentum
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Glycine max (G. soja)
Duration:
22 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Lolium perenne
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL 760 - 3300
Species:
Avena sativa
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Sinapis alba
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Lycopersicon esculentum
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Glycine max (G. soja)
Duration:
22 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
seedling emergence
Remarks on result:
other: 95% CL not reported
Species:
Lolium perenne
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
990 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95% CL 760 - 3300
Species:
Avena sativa
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95% CL not reported
Species:
Sinapis alba
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95% CL not reported
Species:
Lycopersicon esculentum
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95% CL not reported
Species:
Glycine max (G. soja)
Duration:
22 d
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95% CL not reported
Species:
Lolium perenne
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
560 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95 % CL 760 - 3300. No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control.
Species:
Avena sativa
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95 % CL not reported. No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control.
Species:
Sinapis alba
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95 % CL not reported. No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control.
Species:
Lycopersicon esculentum
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95 % CL not reported. No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control.
Species:
Glycine max (G. soja)
Duration:
22 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
growth
Remarks on result:
other: 95 % CL not reported. No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control.
Details on results:
Range-finding Test
A summary of the percentage emergence and mortality and morphological effects for each species during the range-finding test is given in Table 2. A slight reduction in vigour was observed at the 1000 mg/kg test concentration compared to the control for mustard, oat and perennial ryegrass.
Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the emergence and shoot dry weight data for each species.
There were no significant differences (P³0.05) between the control and all the test groups in terms of emergence for each species.
There were no significant decreases in shoot dry weight (P³0.05) between the control and all the test groups at test termination for each species.
Based on this information, test concentration of 100, 180, 320, 560 and 1000 mg/kg were selected for each species for the definitive test.
Definitive Test
Emergence Data
Soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and perennial ryegrass (Lolium perenne) reached 50% emergence in the control on Days 9, 10, 4, 5 and 7 after sowing, respectively.
A summary of the percentage emergence for each species are given in Tables 3 to 7.
Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the emergence data for each species.
There were no significant differences (P³0.05) between the control and all the test groups in terms of emergence for soybean, tomato, oat and perennial ryegrass.
The statistical analysis of the emergence data for mustard did show a significant difference between the control and the 1000 mg/kg test group in terms of the number of plants emerged. On review of the data this was considered to be due to 100% emergence in the control and 100 to 560 mg/kg test groups and 90% emergence in the 1000 mg/kg test group. As only two seedlings failed to emerge in the 1000 mg/kg test group this was considered not to be a true toxic effect but rather a factor of the statistical analysis. It was therefore considered that the test item did not have an effect on the emergence for mustard.
Inspection of the emergence data based on the nominal test concentrations gave the following results:
Species
EC50 (emergence) (mg/kg)
Soybean
>1000
Tomato
>1000
Mustard
>1000
Oat
>1000
Perennial Ryegrass
>1000
The No Observed Effect Concentration for each species was 1000 mg/kg. The No Observed Effect Concentration is based upon no significant differences (P³0.05) between the test concentrations and the control.
Morphological Effects
A summary of any morphological abnormalities (for example, chlorosis or necrosis of the leaves) and percentage mortality, for each species is given in Table 8.
No morphological abnormalities were observed for soybean, tomato and perennial ryegrass throughout the test.
A slight reduction in vigour was observed at 1000 mg/kg for oat and at 320, 560 and 1000 mg/kg for mustard.
Shoot Dry Weight Data
Shoot mean dry weight values for each species are given in Tables 9 to 13. Individual values for shoot dry weights are given in Appendix 1.
Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the shoot dry weight data for each species.
There were no significant differences (P³0.05) between the control and all the test groups in terms of shoot dry weights at test termination for tomato.
There was no significant decrease in shoot dry weight (P³0.05) between the control and all the test groups in terms of shoot dry weights at test termination for soybean, mustard and oat.
A significant increase in shoot dry weight was observed at test concentrations of 100, 180 and 560 mg/kg for soybean, 560 mg/kg for mustard and 100 mg/kg for oat. Given that the effect observed was not a detrimental effect, this was considered not to affect the outcome of the study.
There was a significant decrease in shoot dry weight (P<0.05) between the control and the 1000 mg/kg test group at test termination for perennial ryegrass.
Inspection of the shoot dry weight data for soybean, tomato, mustard and oat and analysis of the shoot dry weight data by the probit method (Finney 1971) for perennial ryegrass based on the nominal test concentrations gave the following results:
Species
EC50 (growth) (mg/kg)
95% Confidence limits
(mg/kg)
Soybean
>1000
-
Tomato
>1000
-
Mustard
>1000
-
Oat
>1000
-
Perennial Ryegrass
990
760 - 3300
 
The No Observed Effect Concentration for soybean, tomato, mustard and oat was 1000 mg/kg. The No Observed Effect Concentration is based upon no significant differences (P³0.05) between the test concentrations and the control in terms of shoot dry weight.
The No Observed Effect Concentration for perennial ryegrass was 560 mg/kg. The No Observed Effect Concentration is based upon significant differences (P<0.05) between the 1000 mg/kg test concentration and the control in terms of shoot dry weight.
Physico-chemical measurements
The temperature was maintained at 7°C to 37°C and the relative humidity at 20% to 89% with a photoperiod of approximately 16 hours light and 8 hours darkness.
Some of the temperatures were observed to be outside the range given in the study plan. This deviation was considered not to affect the integrity or the outcome of the study as no morphological abnormalities were observed in the control plants.
Results with reference substance (positive control):
Due to the tabular form of some of the results please see "any other information on results" section

For all tables see attachments:

Range-finding Test

A summary of the percentage emergence and mortality and morphological effects for each species during the range-finding test is given in Table 2. A slight reduction in vigour was observed at the 1000 mg/kg test concentration compared to the control for mustard, oat and perennial ryegrass.

Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the emergence and shoot dry weight data for each species.

There were no significant differences (P³0.05) between the control and all the test groups in terms of emergence for each species.

There were no significant decreases in shoot dry weight (P³0.05) between the control and all the test groups at test termination for each species.

Based on this information, test concentration of 100, 180, 320, 560 and 1000 mg/kg were selected for each species for the definitive test.

Definitive Test

Emergence Data

Soybean (Glycine max), tomato (Lycoperisicon esculentum), mustard (Sinapis alba), oat (Avena sativa) and perennial ryegrass (Lolium perenne) reached 50% emergence in the control on Days 9, 10, 4, 5 and 7 after sowing, respectively.

A summary of the percentage emergence for each species are given in Tables 3 to 7.

Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the emergence data for each species.

There were no significant differences (P³0.05) between the control and all the test groups in terms of emergence for soybean, tomato, oat and perennial ryegrass.

The statistical analysis of the emergence data for mustard did show a significant difference between the control and the 1000 mg/kg test group in terms of the number of plants emerged. On review of the data this was considered to be due to 100% emergence in the control and 100 to 560 mg/kg test groups and 90% emergence in the 1000 mg/kg test group. As only two seedlings failed to emerge in the 1000 mg/kg test group this was considered not to be a true toxic effect but rather a factor of the statistical analysis. It was therefore considered that the test item did not have an effect on the emergence for mustard.

Inspection of the emergence data based on the nominal test concentrations gave the following results:

Species

EC50(emergence) (mg/kg)

Soybean

>1000

Tomato

>1000

Mustard

>1000

Oat

>1000

Perennial Ryegrass

>1000

The No Observed Effect Concentration for each species was 1000 mg/kg. The No Observed Effect Concentration is based upon no significant differences (P³0.05) between the test concentrations and the control.

Morphological Effects

A summary of any morphological abnormalities (for example, chlorosis or necrosis of the leaves) and percentage mortality, for each species is given in Table 8.

No morphological abnormalities were observed for soybean, tomato and perennial ryegrass throughout the test.

A slight reduction in vigour was observed at 1000 mg/kg for oat and at 320, 560 and 1000 mg/kg for mustard.

Shoot Dry Weight Data

Shoot mean dry weight values for each species are given in Tables 9 to 13. Individual values for shoot dry weights are given in Appendix 1.

Statistical analysis using Bartlett's test for homogeneity of variance (Sokal and Rohlf 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett 1955) was carried out on the shoot dry weight data for each species.

There were no significant differences (P³0.05) between the control and all the test groups in terms of shoot dry weights at test termination for tomato.

There was no significant decrease in shoot dry weight (P³0.05) between the control and all the test groups in terms of shoot dry weights at test termination for soybean, mustard and oat.

A significant increase in shoot dry weight was observed at test concentrations of 100, 180 and 560 mg/kg for soybean, 560 mg/kg for mustard and 100 mg/kg for oat. Given that the effect observed was not a detrimental effect, this was considered not to affect the outcome of the study.

There was a significant decrease in shoot dry weight (P<0.05) between the control and the 1000 mg/kg test group at test termination for perennial ryegrass.

Inspection of the shoot dry weight data for soybean, tomato, mustard and oat and analysis of the shoot dry weight data by the probit method (Finney 1971) for perennial ryegrass based on the nominal test concentrations gave the following results:

Species

EC50(growth) (mg/kg)

95% Confidence limits
(mg/kg)

Soybean

>1000

-

Tomato

>1000

-

Mustard

>1000

-

Oat

>1000

-

Perennial Ryegrass

990

760 - 3300

 

The No Observed Effect Concentration for soybean, tomato, mustard and oat was 1000 mg/kg. The No Observed Effect Concentration is based upon no significant differences (P³0.05) between the test concentrations and the control in terms of shoot dry weight.

The No Observed Effect Concentration for perennial ryegrass was 560 mg/kg. The No Observed Effect Concentration is based upon significant differences (P<0.05) between the 1000 mg/kg test concentration and the control in terms of shoot dry weight.

Physico-chemical measurements

The temperature was maintained at 7°C to 37°C and the relative humidity at 20% to 89% with a photoperiod of approximately 16 hours light and 8 hours darkness.

Some of the temperatures were observed to be outside the range given in the study plan. This deviation was considered not to affect the integrity or the outcome of the study as no morphological abnormalities were observed in the control plants.

Validity criteria fulfilled:
yes
Conclusions:
The EC50 (emergence) and EC50 (growth based on final dry weight) for the test item based on nominal test concentrations for the five species tested were as follows:

Species EC50 (emergence)(mg/kg) NOEC (mg/kg) EC50 (growth) mg/kg) NOEC (mg/kg)

Soybean >1000 1000 >1000 1000
Tomato >1000 1000 >1000 1000
Mustard >1000 1000 >1000 1000
Oat >1000 1000 >1000 1000
Perennial Ryegrass >1000 1000 990 (95% CI: 760-3300) 560
Executive summary:

SUMMARY

Introduction.

A study was performed to assess the effects of the test item on the emergence and growth of five plant species. The method followed that described in the OECD Guidelines for the Testing of Chemicals: Guideline 208: Terrestrial (Non-target) Plant Test: Seedling Emergence and Seedling Growth Test (July 2006).

Methods.

Following a preliminary range-finding test, five plant species; three dicotyledonous species, soybean (Glycine max), tomato (Lycopersicon esulentum) and mustard (Sinapis alba) and two monocotyledonous species, oat (Avena sativa) and perennial ryegrass (Lolium perenne) were exposed to concentrations of 100, 180, 320, 560 and 1000 mg/kg. The number of seedlings emerged and any mortalities and/or morphological abnormalities were determined daily for 21 or 22 days after 50% emergence in the control for each species.

Results.

The EC50(emergence) and EC50(growth based on final dry weight) for the test item based on nominal test concentrations for the five species tested were as follows:

Species

EC50(emergence) (mg/kg)

No Observed Effect Concentration (mg/kg)

EC50

(growth) (mg/kg)

95% Confidence limits
(mg/kg)

No Observed Effect Concentration (mg/kg)*

Soybean

>1000

1000

>1000

-

1000

Tomato

>1000

1000

>1000

-

1000

Mustard

>1000

1000

>1000

-

1000

Oat

>1000

1000

>1000

-

1000

Perennial Ryegrass

>1000

1000

990

760 - 3300

560


*No Observed Effect Concentration (growth) based on the concentration where no significant decrease was observed for dry weight compared to the control

Description of key information

(21 or 22 d) EC50 of ≥1000 mg/kg soil dw; G. max, L. esulentum, S. alba, A. sativa, L. perenne (OECD 208; same results for test mat. 'Distillates (Fischer-Tropsch), C8-26 - branched and linear' and 'Distillates (Fischer-Tropsch), heavy, C18-50 - branched, cyclic and linear')

Key value for chemical safety assessment

Short-term EC50 or LC50 for terrestrial plants:
1 000 mg/kg soil dw
Long-term EC10, LC10 or NOEC for terrestrial plants:
1 000 mg/kg soil dw

Additional information

No terrestrial plants growth tests are available for the substance 'Paraffin waxes (Fischer–Tropsch), full-range, C15–C50 branched and linear':

Five plant species, three dicotyledonous species, soybean (Glyicine max), tomato (Lycopersicon esulentum) and mustard (Sinapis alba) and two monocotyledonous species, oat (Avena sativa) and perennial ryegrass (Lolium perenne) were exposed to the closely related substance GTL Base Oil Distillates (covering the carbon range from C18 to C50) at concentrations of 100, 180, 320, 560 and 1000 mg/kg dw in a seedling emergence and growth test. The study was conducted according to OECD 208 and to GLP, however no analytical monitoring was carried out (Goodband, 2011d).

The number of seedlings which emerged, mortalities and morphological abnormalities were recorded daily for 21 or 22 days after 50% emergence in the controls for each species. It was not possible to establish an EC50with these species and NOEC values have been reported to be at least 1000 mg/kg soil dw for all the organisms tested and across all endpoints.

A similar seedling emergence and seeding growth test is also available for the supporting substance GTL Gasoil covering the carbon range from C8 to C26 (Goodband, 2011b). The test was conducted in accordance with OECD 208 and GLP, however no analytical monitoring of the test substance in the exposure medium was carried out.

The same five species of plant were tested. The lowest EC50 was 990 mg/kg soil dw and the lowest NOEC was 560 mg/kg soil dw with perennial ryegrass.

Conclusion:

Terrestrial plant toxicity data are available for two GTL-derived substances in the relevant carbon number range for

'Paraffin waxes (Fischer–Tropsch), full-range, C15–C50 branched and linear'.

In the absence of adverse effects in any of these studies, based on weight of evidence it can be concluded that the NOEC for the registered substance is ≥1000 mg/kg soil dw.