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Ecotoxicological information

Short-term toxicity to aquatic invertebrates

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Link to relevant study record(s)

Reference
Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
22/02/2005 - 04/05/2005
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
other: ISO 14669 (1999) Water Quality - Determination of acute lethal toxicity to marine cope
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: ISO 5667-16 (1998) Water Quality Sampling - Guidance on biotesting of samples
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Specific details on test material used for the study:
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Solubility and stability of the test substance in the solvent/vehicle: Dissolved at 10 000 mg/L


TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: Dissolved in seawater
- Final preparation of a solid: Dissolved in seawater

FORM AS APPLIED IN THE TEST (if different from that of starting material) Aqueous, in solution


Analytical monitoring:
no
Details on sampling:
- Concentrations: 1000, 1800, 3200, 5600, 10 009 mg/L (nominal concentrations)
- Sampling method: Mortality within a control
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Test material dissolved in seawater
- Controls: 4 mortality controls (1 replicate each). 5 positive controls of 0.1, 0.32, 0.56, 1.0 and 1.8 mg/L (2 replicates per concentration).


Test organisms (species):
other aquatic crustacea: Acartia tonsa
Details on test organisms:
TEST ORGANISM
- Common name: Acartia tonsa

ACCLIMATION
- Acclimation period:
- Acclimation conditions (same as test or not): No
- Type and amount of food: Mixed algal diet (2-4 species)

Test type:
static
Water media type:
saltwater
Limit test:
no
Total exposure duration:
48 h
Remarks on exposure duration:
Measurements taken at 24 and 48 hours.
Test temperature:
17.9 - 21.3 °C
pH:
At 0 hours, pH 8.09-8.13
At 48 hours, pH 7.99-8.13
Dissolved oxygen:
94-97%
Conductivity:
48.5-49.7 mS/cm.
Nominal and measured concentrations:
Nominal concentrations for test substance were 1000, 1800, 3200, 5600, 10 009 mg/L
Details on test conditions:
TEST SYSTEM
- Test vessel: crystallising dishes
- Type (delete if not applicable) closed, soda glass watch cover
- Material, size, headspace, fill volume: borosilicate glass, 50 ml
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 4

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Natural seawater from Scapa Flow, Orkney.
- Particulate matter: Filtered seawater
- Conductivity: 48.0 - 49.9 mS/cm
- Culture medium different from test medium: Yes
- Intervals of water quality measurement: Daily


EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Mortality of population over time.

RANGE-FINDING STUDY
- Test concentrations: Nominal concentrations 1, 10, 100, 1000 mg/ L
- Results used to determine the conditions for the definitive study: Yes
Reference substance (positive control):
yes
Remarks:
3,5 Dichlorophenol
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
2 675 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Key result
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
1 553.85 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Duration:
48 h
Dose descriptor:
other: LC90
Effect conc.:
2 733.33 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Details on results:
- Mortality of control: 0%
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: No
- Effect concentrations exceeding solubility of substance in test medium: No
Results with reference substance (positive control):
- Results with reference substance valid? Yes
- Limit test: No
- Dose-response test: Yes, 1.8, 1.0, 0.56, 0.32 and 0.1 mg/L
- ECx: LC50
Validity criteria fulfilled:
yes
Conclusions:
The test substance has a LC50 of 2675.00 mg/L for 24 hours and 1553.85 mg/L for 48 hours, an LC90 value of 2733.33 mg/L for 48 hours and a NOEC value of 1000.00 mg/L for 48 hours.
Executive summary:

The study assessed the short-term toxicity of monoethanolamine salt of nitrilotriacetic acid to aquatic invertebrates. This study was performed in compliance with GLP and follows the guidelines of ISO 14669 (1999) Water Quality - Determination of acute lethal toxicity to marine copepods (Copepoda; Crustacea) and ISO 5667 - 16 (1998) Water Quality Sampling - Guidance on biotesting of samples.

All validity criteria were met and the test organisms used was Acartia tonsa. The rangefinding test exhibited no effect at the maximum concentration (0% proportional mortality response at 48 hours). Therefore, in the definitive test nominal concentrations of 1000, 1800, 3200, 5600, 10 000 mg/L were used with 2 replicates per concentration per time point measured (10 organisms per replicate). Four mortality controls were present (0 mg/L test material) which showed a proportional mortality response of 0% over 48 hours for 1 replicate per concentration, each with 10 -11 organisms. Five positive controls were present (0.1, 0.32, 0.56, 1.0 and 1.8 mg L-1 3,5 Dichlorophenol) with 2 replicates per concentration each with 9 - 11 organisms per replicate giving a 48 hour LC50 value of 0.51 mg/L. Monoethanolamine Salt of Nitrilotriacetic Acid exhibited a 48h LC50 value of 1553.85 mg/L (dilution series) to the marine copepod Acartia tonsa in the aqueous phase.

Description of key information

The study assessed the short-term toxicity of monoethanolamine salt of nitrilotriacetic acid to aquatic invertebrates. This study was performed in compliance with GLP and follows the guidelines of ISO 14669 (1999) Water Quality - Determination of acute lethal toxicity to marine copepods (Copepoda; Crustacea) and ISO 5667 - 16 (1998) Water Quality Sampling - Guidance on biotesting of samples.

All validity criteria were met and the test organisms used was Acartia tonsa. The rangefinding test exhibited no effect at the maximum concentration (0% proportional mortality response at 48 hours). Therefore, in the definitive test nominal concentrations of 1000, 1800, 3200, 5600, 10 000 mg/L were used with 2 replicates per concentration per time point measured (10 organisms per replicate). Four mortality controls were present (0 mg/L test material) which showed a proportional mortality response of 0% over 48 hours for 1 replicate per concentration, each with 10 -11 organisms. Five positive controls were present (0.1, 0.32, 0.56, 1.0 and 1.8 mg/L 3,5 Dichlorophenol) with 2 replicates per concentration each with 9 - 11 organisms per replicate giving a 48 hour LC50 value of 0.51 mg/L. Monoethanolamine Salt of Nitrilotriacetic Acid exhibited a 48h LC50 value of 1553.85 mg/L (dilution series) to the marine copepod Acartia tonsa in the aqueous phase.

Key value for chemical safety assessment

Marine water invertebrates

Marine water invertebrates
Effect concentration:
1 553.85 mg/L

Additional information