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EC number: 919-489-5 | CAS number: -
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
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Sediment toxicity
Administrative data
Link to relevant study record(s)
- Endpoint:
- sediment toxicity: long-term
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2018-01-23 to 2018-05-02
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 225 (Sediment-Water Lumbriculus Toxicity Test Using Spiked Sediment)
- Version / remarks:
- 2007
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- SEDIMENT
- Concentrations: all
- Sampling interval: day 0,7, and 28
PORE WATER
- Concentrations: all
- Sampling interval: day 0,7, and 28
OVERLYING WATER
- Concentrations: all
- Sampling interval: day 0,7, and 28 - Vehicle:
- yes
- Remarks:
- Acetone
- Details on sediment and application:
- PREPARATION OF SPIKED SEDIMENT
The respective test item amount was weighed out for a stock solution and dissolved in Acetone. The stock solution was further diluted with Acetone to receive the respective application solutions. The appropriate amount of spiking solution (2.5 mL per replicate) was thoroughly mixed with a sub-quantity of the artificial sediment (10 g per replicate). After complete evaporation of the solvent, the spiked portion of artificial sediment was thoroughly mixed with the remaining sediment. Demineralised water was added to the artificial sediment to adjust the humidity of the artificial sediment to a moisture of 30 %. Subsequently, the test medium was thoroughly mixed to ensure a homogenous distribution and about 45 g soil dry weight was filled into test vessels. - Test organisms (species):
- Lumbriculus variegatus
- Details on test organisms:
- TEST ORGANISM
- Strain/clone: Müller
- Justification for species other than prescribed by test guideline: Lumbriculus variegatus is the recommended species according to the guideline.
- Breeding conditions: Breeding is performed at the test facility at 20 ± 2 °C and diffuse light (100 - 500 lx, photoperiod 16 h light daily). The dissolved oxygen concentration is > 70 % of the air saturation value corresponding to 6.2 mg O2/L. All worms used in the test originated from the same delivery of the supplier and the same stock.
- Medium: Breeding of L. variegatus is performed on quartz sand in reconstituted water containing 125 mL from each stock solution poured in a can and filled up to 25 L with demineralised water.
- Feeding during breeding: TetraMin® flake food (Tetra) is provided twice per week.
- Feeding during test: Powder of Urtica dioica (stinging nettle, Heinrich Klenk GmbH & Co KG, 97525 Schwebheim, Germany) was mixed into the sediment at the day of application. The amount was 0.4 % of the sediment dry weight. - Study type:
- laboratory study
- Test type:
- static
- Water media type:
- freshwater
- Type of sediment:
- artificial sediment
- Limit test:
- no
- Duration:
- 28 d
- Exposure phase:
- total exposure duration
- Post exposure observation period:
- not applicable
- Test temperature:
- Room or Water temperature 20 ± 2 °C
- pH:
- Sediment at start: 6.78
- Dissolved oxygen:
- Above 70 % of the air saturation value corresponding to 6.2 mg/L O2 (internal quality criterion).
- Nominal and measured concentrations:
- Nominal test item concentration: control, solvent control, 0.645, 1.75, 4.81, 13.2, 36.4, 100 mg/kg dw
- Details on test conditions:
- TEST SYSTEM
- Test container: 250 mL glass beakers (6 cm diameter)
- Sediment volume: 45 g dry weight per vessel / ca. 1.0 - 3.0 cm from the ground
- Overlying water volume: per replicate 150 mL
- Depth of sediment and overlying water: Water levels were topped up with demineralised water each working day during the study to compensate losses due to evaporation.
- Aeration: yes, gentle aeration via Pasteur pipettes. Aeration was checked each working day.
EXPOSURE REGIME
- No. of organisms per container (treatment): 10 synchronised worms
- No. of replicates per treatment group: 4 replicates per treatement group, one additional replicate for analytical measurements on day 0, 7, 28 each
- No. of replicates per control / vehicle control: 6 replicates per control, one additional replicate for analytical measurements on day 0, 7, 28 each
- Feeding regime: Powder of Urtica dioica (stinging nettle, Heinrich Klenk GmbH & Co KG, 97525 Schwebheim, Germany) was mixed into the sediment at the day of application. The amount was 0.4 % of the sediment dry weight.
OVERLYING WATER CHARACTERISTCS
- Type of water: demineralised water
- Total organic carbon: 2.13 %
CHARACTERIZATION OF SEDIMENT
Artificial sediment containing:
- 4.17 % peat, air-dried and finely ground
- 20 % kaolin, with a kaolinite content > 30 %
- 75 % quartz sand (> 50 % particles sized 50-200 pm)
- 0.35 % calcium carbonate (CaCC>3) to achieve a pH of 6.78
The organic carbon content of the final mixture was 2.13 %.
OTHER TEST CONDITIONS
- Photoperiod: 16 h light, 8 h dark
- Light intensity: 100 - 500 lx
EFFECT PARAMETERS MEASURED:
Visual observations of behavioural differences to the control were recorded three times per week. The endpoints of the study as determined after day 28 were the number of surviving worms per replicate and the total dry biomass of worms per replicate. Worms were considered dead if showing no response to a mechanical stimulus, signs of decomposition or by absence. Living worms were assigned as complete worms or incomplete worms.
VEHICLE CONTROL PERFORMED: yes
TEST CONCENTRATIONS
- Test concentrations and Spacing factor for test concentrations: 0.64 - 1.75 - 4.81 - 13.2 - 36.4 - 100 mg/kg sediment dry weight (factor 2.75). - Reference substance (positive control):
- yes
- Remarks:
- A reference item study is performed once a year with Potassium chloride. The most recent reference item test was carried out from 2017-03-01 and 2017-03-29.
- Key result
- Duration:
- 28 d
- Dose descriptor:
- LOEC
- Effect conc.:
- 100 mg/kg sediment dw
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: total number of worms/Reproduction, Biomass
- Key result
- Duration:
- 28 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 36.4 mg/kg sediment dw
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Total number of worms/Reproduction, Biomass
- Key result
- Duration:
- 28 d
- Dose descriptor:
- EC10
- Effect conc.:
- 26.3 mg/kg sediment dw
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- reproduction
- Remarks on result:
- other: confidence interval: 12.1 - 41.5
- Key result
- Duration:
- 28 d
- Dose descriptor:
- EC10
- Effect conc.:
- 51.9 mg/kg sediment dw
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Remarks on result:
- other: confidence interval: 30.8 - n.d.
- Details on results:
- - Mortality:
No mortality of worms was observed in the controls and all test item concentrations after exposure to the test item over 28 days. Since no statistically significant difference was found between the control and the solvent control, both controls were pooled for further evaluation. The total number of worms and thus the reproduction did not statistically significantly differ compared to the pooled control in the test item concentrations 0.64 to 36.4 mg/kg sediment dry weight. However, at the test item concentration 100 mg/kg sediment dry weight the total number of worms and thus the reproduction was statistically significantly reduced.
- Behaviour and pathological Symptoms:
No evident changes in the worm behaviour or pathological symptoms were observed in the control as well as in all test item concentrations during the 28 days of exposure
- Dry Biomass of the Worms per Replicate:
At test start the worms had a body weight of 12.1 mg dry weight/10 worms (mean weight of two determinations). At test end, the mean biomass dry weight of the worms was not statistically significantly different at the test item concentrations 0.64 to 36.4 mg/kg soil dry weight compared to the pooled control. However, at the test item concentration 100 mg/kg soil dry weight the mean biomass dry weight of the worms was statistically significantly reduced.
- Measured Exposure Concentrations:
Analytical evaluation of the test item and control was carried out via GC-MS/MS for sediment layer, aqueous phase and pore water on day 0, day 7 and day 28. The measured concentrations of the test item in the sediment were in the ranges from 75% to 107% at day 0, from 68% to 88% at day 7 and from 52% to 73% of the nominal concentrations at day 28. No recoveries of the concentrations of the test item in the aqueous phase and pore water could be determined. Control and solvent control samples were < LOQ, except on day 0 in the control due to carry-over effects within the sample preparation.
- Validity Criteria:
The study was performed according to OECD guideline 225 (2007) and GLP principles. The results met the validity criteria in all points:
- During the test, the oxygen concentration was > 30 % of the air saturation value, corresponding to 2.7 mg/L O2.
- The pH-value was between 6 and 9 in the overlying water during the test.
- In the control group the average number of living worms per replicate increased by a factor of at least 1.8. - Results with reference substance (positive control):
- - Results with reference substance valid: yes
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on results of an OECD 225 compliant study with the test item an EC10 (reproduction) of 26.3 mg/kg sediment dw was determined as key value.
- Executive summary:
The effects of the test item on the oligochaete Lumbriculus variegatus in a water-sediment system were determined. The study was carried out according to OECD Guideline 225 (2007). The test duration was 28 days from the insertion of the test organisms. The study was performed by spiking artificial sediment with the test item concentrations 0.64 - 1.75 -4.81 - 13.2 - 36.4 - 100 mg/kg sediment dry weight. A control using untreated artificial sediment as well as a solvent control using artificial sediment treated with the solvent were set up. Six replicates per control and solvent control and four replicates per test item concentration were set up for biological investigations. Water quality parameters (temperature, pH-value, O2-concentration, ammonium and total hardness) were determined throughout the study using an additional replicate for the controls and the test item concentrations, each. Three additional replicates for chemical analysis on day 0, day 7 and day 28 were set up for the controls and each test item concentration. Analytical evaluation of the test item and control was carried out via GC-MS/MS for sediment layer, aqueous phase and pore water on day 0, day 7 and day 28. Details of the analytical method are presented in part 13. The measured concentrations of the test item in the sediment were in the ranges from 75% to 107% at day 0, from 68% to 88% at day 7 and from 52% to 73% of the nominal concentrations at day 28. No recoveries of the concentrations of the test item in the aqueous phase and pore water were determined. Control and solvent control samples were < LOQ, except on day 0 in the control due to carry-over effects within the sample preparation. After 28 days of exposure, induced no mortality in all test item concentrations. Since no statistically significant difference between the control and the solvent control was determined, both controls were pooled for further evaluation.
The total number of worms and thus the reproduction did not statistically significantly differ compared to the pooled control in the test item concentrations 0.64 to 36.4 mg/kg sediment dry weight. However, at the test item concentration 100 mg/kg sediment dry weight the total number of worms was statistically significantly reduced. Compared to the pooled control, the total biomass per replicate was not statistically significantly different in the test item concentrations 0.64 to 36.4 mg/kg sediment dry weight. However, at the test item concentration 100 mg/kg sediment dry weight the total biomass per replicate was statistically significantly reduced. All validity criteria were fulfilled.
NOEC (Total number of worms/Reproduction, Biomass): 36.4 mg/kg sediment dry weight
EC Total number of worms/Reproduction (Confidence lntervall): EC10: 26.3 (12.1 -41.5); EC20: 45.1 (32.2-67.4); EC50: > 100 (80.8 - n.d.)
EC Total Biomass per replicate (Confidence lntervall): EC10: 51.9 (30.8-n.d.); EC20: 72.4 (45.5-n.d.); EC50: > 100 (91.2-n.d.)
Reference
Table 1 Summary of all Effect-levels
Effects |
Test item [mg/kg sediment dry weight] |
LOEC (Total number of worms/Reproduction, Biomass) |
100 |
NOEC (Total number of worms/Reproduction, Biomass) |
36.4 |
EC Total number of worms/Reproduction (Confidence lntervall) |
EC10: 26.3 (12.1 -41.5) EC20: 45.1 (32.2 -67.4) EC50: > 100 (80.8 - n.d.) |
EC Total Biomass per replicate (Confidence lntervall) |
EC10: 51.9 (30.8-n.d.) EC20: 72.4 (45.5 -n.d.) EC50: > 100 (91.2-n.d.) |
Table 2: Mortality after 28 days of exposure
Test item concentration |
Number of Dead or Missing Worms Mean Value |
Mortality (%) |
Control |
0 |
0 |
Solvent Control |
0 |
0 |
0.64 |
0 |
0 |
1.75 |
0 |
0 |
4.81 |
0 |
0 |
13.2 |
0 |
0 |
36.4 |
0 |
0 |
100 |
0 |
0 |
Table 3: Total worm number after 28 days of exposure
Test item concentration |
Number of Surviving Worms Mean Value |
Standard Deviation |
Inhibition to pooled control (%) |
Sign.* |
Control |
35.8 |
5.00 |
- |
- |
Solvent Control |
33.8 |
3.06 |
- |
- |
Pooled Control |
34.8 |
4.09 |
- |
- |
0.64 |
39.0 |
3.74 |
-12.0 |
No |
1.75 |
30.5 |
7.94 |
12.4 |
No |
4.81 |
34.5 |
3.51 |
0.95 |
No |
13.2 |
32.0 |
3.92 |
8.13 |
No |
36.4 |
32.0 |
3.56 |
8.13 |
No |
100 |
18.0 |
2.31 |
48.3 |
Yes |
*= statistically significantly different compared to pooled control (Williams Multiple Sequential t-test procedure, alpha = 0.05)
Table 4: Reproduction after 28 days of exposure
Test item concentration |
Number of Reproduced Worms Mean Value |
Standard Deviation |
Inhibition to pooled control (%) |
Sign.* |
Control |
25.8 |
5.00 |
- |
- |
Solvent Control |
23.8 |
3.06 |
- |
- |
Pooled Control |
24.8 |
4.09 |
- |
- |
0.64 |
29.0 |
3.74 |
-16.8 |
No |
1.75 |
20.5 |
7.94 |
17.4 |
No |
4.81 |
24.5 |
3.51 |
1.33 |
No |
13.2 |
22.0 |
3.92 |
11.4 |
No |
36.4 |
22.0 |
3.56 |
11.4 |
No |
100 |
8.00 |
2.31 |
67.8 |
Yes |
*= statistically significantly different compared to pooled control (Williams Multiple Sequential t-test procedure, alpha = 0.05)
Table 6: Worm dry biomass after 28 days of exposure
Test item concentration |
Dry weight (mg) per replicate Mean Value |
Standard Deviation |
Inhibition to pooled control (%)# |
Sign.* |
Control |
24.7 |
9.0 |
- |
- |
Solvent Control |
24.8 |
3.1 |
- |
- |
Pooled Control |
24.7 |
6.4 |
- |
- |
0.64 |
29.1 |
3.5 |
-17.8 |
No |
1.75 |
19.8 |
9.0 |
20.1 |
No |
4.81 |
31.2 |
2.6 |
-27.4 |
No |
13.2 |
27.3 |
1.6 |
-10.4 |
No |
36.4 |
27.2 |
0.8 |
-10.2 |
No |
100 |
15.3 |
4.8 |
38.2 |
Yes |
*= statistically significantly different compared to pooled control (Dunnett’s Method)
#) negative value = increase of worm dry biomasse
Table 5: Worm behaviour during 28 days of exposure
Nominal concentration |
Effect |
Days after addition |
||||||||||||
0 |
2 |
5 |
7 |
9 |
12 |
14 |
16 |
19 |
21 |
23 |
26 |
28 |
||
|
Number of replicates (out of 6 or 4 replicates) showing particular feature |
|||||||||||||
Control |
ob a f |
6 - - |
5 1 1 |
5 1 6 |
3 3 5 |
3 3 6 |
5 1 6 |
1 5 6 |
3 3 6 |
6 - 6 |
6 - 6 |
5 1 6 |
6 - 6 |
5 1 6 |
Solvent Control |
ob a f |
6 - - |
6 - 1 |
5 1 6 |
4 2 4 |
3 3 5 |
6 - 6 |
5 1 6 |
5 1 6 |
5 1 6 |
4 2 6 |
5 1 6 |
6 - 6 |
6 - 6 |
0.64 |
ob a f |
4 - - |
3 1 - |
2 2 4 |
4 - 1 |
4 - 4 |
4 - 4 |
3 1 4 |
2 2 4 |
3 1 4 |
4 - 4 |
3 1 4 |
3 1 4 |
4 - 4 |
1.75 |
ob a f |
2 2 - |
3 1 1 |
4 - 4 |
3 1 3 |
3 1 4 |
2 2 4 |
2 2 4 |
2 2 4 |
3 1 4 |
4 - 4 |
4 - 4 |
4 - 4 |
4 - 4 |
4.81 |
ob a f |
4 - - |
3 1 3 |
4 - 4 |
3 1 2 |
3 1 4 |
4 - 4 |
3 1 4 |
3 1 4 |
4 - 4 |
4 - 4 |
4 - 4 |
4 - 4 |
4 - 4 |
13.2 |
ob a f |
3 1 - |
4 - 1 |
3 1 4 |
3 1 3 |
1 3 4 |
3 1 4 |
2 2 4 |
4 - 4 |
3 1 4 |
4 - 4 |
4 - 4 |
3 1 4 |
4 - 4 |
36.4 |
ob a f |
4 - - |
4 - 4 |
3 1 4 |
3 1 4 |
3 1 4 |
1 3 4 |
3 1 4 |
3 1 4 |
4 - 4 |
2 2 4 |
4 - 4 |
4 - 4 |
3 1 4 |
100 |
ob a w f |
1 3 - - |
1 3 - - |
2 2 - 4 |
- 4 2 4 |
1 3 - 4 |
2 2 - 4 |
2 2 - 4 |
3 1 - 4 |
3 1 - 4 |
2 2 - 4 |
3 1 - 4 |
2 2 - 4 |
2 2 - 4 |
a) worm on sediment surface ob) no abnormality detected f) faeces on the sediment surface
w) worm in water phase -) no observation
Description of key information
Based on results of an OECD 225 compliant study with the test item an EC10 (reproduction) of 26.3 mg/kg sediment dw was determined as key value.
Key value for chemical safety assessment
- EC10, LC10 or NOEC for freshwater sediment:
- 26.3 mg/kg sediment dw
Additional information
The effects of the test item on the oligochaete Lumbriculus variegatus in a water-sediment system were determined. The study was carried out according to OECD Guideline 225 (2007). The test duration was 28 days from the insertion of the test organisms. The study was performed by spiking artificial sediment with the test item concentrations 0.64 - 1.75 -4.81 - 13.2 - 36.4 - 100 mg/kg sediment dry weight. A control using untreated artificial sediment as well as a solvent control using artificial sediment treated with the solvent were set up. Six replicates per control and solvent control and four replicates per test item concentration were set up for biological investigations. Water quality parameters (temperature, pH-value, O2-concentration, ammonium and total hardness) were determined throughout the study using an additional replicate for the controls and the test item concentrations, each. Three additional replicates for chemical analysis on day 0, day 7 and day 28 were set up for the controls and each test item concentration. Analytical evaluation of the test item and control was carried out via GC-MS/MS for sediment layer, aqueous phase and pore water on day 0, day 7 and day 28. Details of the analytical method are presented in part 13. The measured concentrations of the test item in the sediment were in the ranges from 75% to 107% at day 0, from 68% to 88% at day 7 and from 52% to 73% of the nominal concentrations at day 28. No recoveries of the concentrations of the test item in the aqueous phase and pore water were determined. Control and solvent control samples were < LOQ, except on day 0 in the control due to carry-over effects within the sample preparation. After 28 days of exposure, induced no mortality in all test item concentrations. Since no statistically significant difference between the control and the solvent control was determined, both controls were pooled for further evaluation.
The total number of worms and thus the reproduction did not statistically significantly differ compared to the pooled control in the test item concentrations 0.64 to 36.4 mg/kg sediment dry weight. However, at the test item concentration 100 mg/kg sediment dry weight the total number of worms was statistically significantly reduced. Compared to the pooled control, the total biomass per replicate was not statistically significantly different in the test item concentrations 0.64 to 36.4 mg/kg sediment dry weight. However, at the test item concentration 100 mg/kg sediment dry weight the total biomass per replicate was statistically significantly reduced. All validity criteria were fulfilled.
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