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Ecotoxicological information

Short-term toxicity to aquatic invertebrates

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Administrative data

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:
04 Feb - 08 Mar 2019
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Version / remarks:
April 2004
GLP compliance:
yes (incl. QA statement)
Analytical monitoring:
yes
Details on sampling:
- Concentrations: Samples were taken initial from the test preparation and from pooled replicates after 48 h.
- Sample storage conditions before analysis: no
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
A nominal amount of test item (100 mg) was dissolved in test water and the volume adjusted to 1 liter to give the 100 mg/L test concentration from which a series of dilutions was made to give further test concentrations of 56, 32, 18 and 10 mg/L.

Test organisms (species):
Daphnia magna
Details on test organisms:
TEST ORGANISM
- Source: in-house labroatory breeding
- Age: less than 24 hours
- Feeding during test: no

CULTURE
- Culture conditions: Same as in test
- Type and amount of food: algal suspension (Pseudokirchneriella subcapitata) and GM300 fish food suspension.
- Feeding frequency: daily
Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Test temperature:
20 - 21 °C
pH:
control: 7.7 - 8.1
test concentrations: 7.9 - 8.4
Dissolved oxygen:
8.4 - 9.5 mg/L
Nominal and measured concentrations:
Nominal test substance concentrations: 10, 18, 32, 56 and 100 mg/L.
Measured test concentrations (initial): 9.89, 15.6, 30.5, 55.5, and 96.2 mg/L
Details on test conditions:
TEST SYSTEM
- Test vessel: glass vessels (50 mL nominal volume)
- Type (delete if not applicable): test vessels were covered
- Fill volume: 100 mL
- Aeration: none
- No. of organisms per vessel:5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4


TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: reconstituted water (Elendt M7 medium)
- Culture medium different from test medium: no
- Intervals of water quality measurement: daily

OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16:8 day/night
- Light intensity: between 200 and 1200 Lux

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : mobility after 24 and 48 hours

RANGE-FINDING STUDY
- Test concentrations: 0.1, 1.0, 10 and 100 mg/L
- Results used to determine the conditions for the definitive study: 100% immobilisation at 100 mg/L
Sub lethal effects of exposure were observed. Trapping at the surface was observed in one control Daphnia and one Daphnia at the test concentration of 10 mg/L was pale.
Reference substance (positive control):
yes
Remarks:
potassium dichromate
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
40 mg/L
95% CI:
>= 35 - <= 46
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
18 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
15.6 mg/L
Nominal / measured:
meas. (initial)
Conc. based on:
test mat.
Basis for effect:
mobility
Details on results:
- Behavioural abnormalities: After 24 h: reduced mobility and pale at 56 mg/L. After 48 h: reduced mobility and pale at 32 and 56 mg/L.
- Mortality of control: no
- Other adverse effects control: Trapping at the surface was observed in one control Daphnia.
Results with reference substance (positive control):
EC50(48 h): 0.80 mg/L
The positive control was conducted between 25 September 2018 and 27 September 2018.
Reported statistics and error estimates:
EC50 values: Probit analysis using Linear Maximum Likelihood regression.
LOEC and NOEC values: Calculated using the ToxRat Professional computer software package (TOXRAT).
Validity criteria fulfilled:
yes
Remarks:
For further details please refer to table 3 in “Any other information on results incl. tables”.

Description of key information

EC50 (48 h): 40 mg/L (nominal), OECD 202

Key value for chemical safety assessment

Additional information