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Ecotoxicological information

Short-term toxicity to aquatic invertebrates

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Reference
Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
25 July 2017 - 03 August 2017
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:
13 April 2004
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
Version / remarks:
30 May 2008
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: OECD Series on Testing and Assessment, No. 23, "Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures''
Version / remarks:
15 December 2000
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: SANCO/3029/99 rev.4 11/07/00: Residues: Guidance for generating and reporting methods of analysis in support of pre-registration data requirements for Annex II (part A; Section 4) and Annex III (part A; Section 5) of directive 91/414
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Remarks:
13 March 2017
Specific details on test material used for the study:
Correction factor for purity: 2.554
Analytical monitoring:
yes
Details on sampling:
- Concentrations: all test concentrations and the control
- Sampling method: at t=0 duplicate samples were taken from the freshly prepared test media, at t=48 duplicate test samples were taken from the test media by pouring together the contents of the test beakers of each treatment.
- Sample storage conditions before analysis: all samples were stored in a freezer (≤ - 20 °C), protected from light until analysis was performed.
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: the test item was applied individually, directly to the test medium. Subsequently, the test solutions were stirred for 10 minutes.
- Controls: In the control, test water was used without addition of the test item.
- Evidence of undissolved material: the test medium at 116.2 mg test item/L (45.5 mg solids/L) appeared to be slightly turbid and caused slight foaming. At 255.4 mg test item/L (100 mg solids/L), slight turbidity and foaming was observed.
Test organisms (species):
Daphnia magna
Details on test organisms:
TEST ORGANISM
- Common name: daphnia
- Clone: 5
- Source: in-house laboratory stock
- Age at study initiation: 1-19 hours old
- Age of parental stock: not indicated
- Feeding during breeding: daphnids in the stock culture were fed at least on all working days with green algae (Desmodesmus subspicatus) freshly grown in the laboratories of the test facility.
- Feeding during test: no

ACCLIMATION: no

METHOD FOR PREPARATION AND COLLECTION OF EARLY INSTARS OR OTHER LIFE STAGES:
The daphnids were bred in the laboratories of the test facility under similar temperature and light conditions as used in the test. The cultivation of the parental daphnids was performed in Elendt M4 medium. The test organisms were not first brood progeny.
Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Hardness:
250 mg CaCO3/L
Test temperature:
20.5 to 20.6 °C at test start;
20.3 to 20.5 °C at test end
pH:
8.0 to 8.1 at test start;
7.9 at test end
Dissolved oxygen:
8.7 to 8.9 mg/L at test start;
8.2 to 8.4 mg/L at test end
Nominal and measured concentrations:
Nominal concentrations: 255.4, 116.2, 52.9, 24.0 and 11.0 mg test item/L (equivalent to 100, 45.5, 20.7, 9.4 and 4.3 mg solids/L)
Measured concentrations: see table 1 in 'any other information on results'
Mean measured concentrations were 84-100% of nominal values.
Details on test conditions:
TEST SYSTEM
- Test vessel: glass beakers of 100 mL, fill volume: 60 mL, covered with a lid
- 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 ''M4'')
- Culture medium different from test medium: no
- Intervals of water quality measurement: water temperature, pH-values and dissolved oxygen concentrations were determined at test start and test end in each treatment group.

OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16 h light : 8 h dark
- Light intensity: 220 to 500 lux

EFFECT PARAMETERS MEASURED: The mobility of the daphnids was determined by visual observation after 24 and 48 hours. Those animals that are not able to swim within 15 seconds after gentle agitation of the test beaker were considered to be immobile (even if they could still move their antennae).

RANGE-FINDING STUDY
- Test concentrations: 0.1, 1, 10 and 100 mg/L
- Results used to determine the conditions for the definitive study: yes, 100% immobilisation was observed in the highest concentration while no immobility was observed in the lower concentrations. Therefore, the EC50 was expected to be between 10 and 100 mg/L.
Reference substance (positive control):
yes
Remarks:
potassium dichromate (January 2017)
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
64.8 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
25.4 mg/L
Nominal / measured:
nominal
Conc. based on:
other: solid fraction
Basis for effect:
mobility
Details on results:
- Abnormalities observed: no
- After 48 hours of exposure no immobilisation of the test animals was observed in the control and up to and including the nominal test item concentration of 24.0 mg test item/L (9.4 mg solids/L). At the nominal concentration of 52.9 mg test item/L (20.7 mg solids/L), 7 animals were immobile and 18 animals were immobile at the nominal concentration of 116.2 mg test item/L (45.5 mg solids/L). At the highest test concentration of 255.4 mg test item/L (100 mg solids/L), 20 daphnids were immobile (see table 2).
- At test end, the test medium appeared to be slightly turbid at 116.2 mg test item/L (45.5 mg solids/L) and turbid at 255.4 mg test item/L (100 mg solids/L)
- The 95% confidence interval for the EC50 was calculated to be 52.7 -79.6 mg/L (20.6 -31.2 mg solids/L)
- Analysis showed that the test concentrations remained 84-100% of nominal test concentrations. Therefore, the effect concentrations were based on nominal test concentrations.
Results with reference substance (positive control):
- Results with reference substance valid? Yes
- Relevant effect levels: 48h-EC50: 1.06 mg/L
- Other: based on the 24h-EC50 of 1.48 mg/L, the sensitivity was according to the proposed OECD levels (24h-EC50 between 0.6 and 2.1 mg potassium dichromate/L).
Reported statistics and error estimates:
The 24-hour and 48-hour EC50, EC20 and EC10 and the 95 % confidence limits were calculated by probit analysis.
The NOEC and LOEC after 24 and 48 hours were determined directly from the raw data.
The software used to perform the statistical analysis was ToxRat Professional, Version 3.2.1, ToxRat Solutions GmbH.

Table 1 Measured concentrations

Sample description

Concentration found

D.F.

Concentration calculated

Concentration nominal

(mg test item/L)

Sampling day

Age (h)

 (mg test item/L)*

1

(mg test item/L)*

 (mg test item/L)

% of nominal*

Control

0

0

<LOD

1

n.a.

0.000

n.a.

Control

0

0

<LOD

1

n.a.

0.000

n.a.

Control

2

48

<LOD

1

n.a.

0.000

n.a.

Control

2

48

<LOD

1

n.a.

0.000

n.a.

11

0

0

9.591

1

9.591

11.000

87

11

0

0

9.943

1

9.943

11.000

90

11

2

48

9.051

1

9.051

11.000

82

11

2

48

9.774

1

9.774

11.000

89

 

 

 

 

 

 

Mean value (n=4):

87

 

 

 

 

 

 

RSD (n=4):

4

24

0

0

20.932

1

20.932

2400

87

24

0

0

20.212

1

20.212

2400

84

24

2

48

19.591

1

19.591

2400

82

24

2

48

20.309

1

20.309

2400

85

 

 

 

 

 

 

Mean value (n=4):

84

 

 

 

 

 

 

RSD (n=4):

3

52.9

0

0

50.787

1

50.787

52.900

96

52.9

0

0

50.447

1

50.447

52.900

95

52.9

2

48

45.703

1

45.703

52.900

86

52.9

2

48

34.483

1

34.483

52.900

#65

 

 

 

 

 

 

Mean value (n=4):

93

 

 

 

 

 

 

RSD (n=4):

6

116.2

0

0

116.167

1

116.167

116.200

100

116.2

0

0

117.555

1

117.555

116.200

101

116.2

2

48

117.310

1

117.310

116.200

101

116.2

2

48

115.433

1

115.433

116.200

99

 

 

 

 

 

 

Mean value (n=4):

100

 

 

 

 

 

 

RSD (n=4):

1

255.4

0

0

126.955

2

253.909

255.400

99

255.4

0

0

125.225

2

250.449

255.400

98

255.4

2

48

118.792

2

237.583

255.400

93

255.4

2

48

122.773

2

245.546

255.400

96

 

 

 

 

 

 

Mean value (n=4):

97

 

 

 

 

 

 

RSD (n=4):

3

 

 

 

 

 

Overall mean value (n=20)

92

 

 

 

 

 

RSD (n=20)

7

* The tabulated results represent rounded results calculated on the exact raw data

LOD: Limit of Detection = 1 mg test item/L

n.a.: not applicable; RSD: Relative Standard Deviation; D.F.: Dilution factor

#considered to be an outlier, not used for calculation

Table 2 Influence of Miranol Ultra C32 on the mobility of Daphnia magna

Nominal concentration (mg test item/L)

No. of Daphnia tested

No. of immobilized Daphnia

% of immobilized Daphnia

 

 

After 24 h

After 48 h

After 24 h

After 48 h

Control

20

0

0

0

0

11

20

0

0

0

0

24

20

0

0

0

0

52.9

20

1

7

5

35

116.2

20

2

18

10

90

255.4

20

1

20

5

100

Validity criteria fulfilled:
yes
Remarks:
See 'overall remarks' section
Conclusions:
The 48h-EC50 for Miranol Ultra C32 towards Daphnia magna was 64.8 mg/L (25.4 mg solids/L).
Executive summary:

A short term toxicity test was performed, according to OECD guideline 202 and GLP principles, to assess the potential of Miranol Ultra C32 to induce immobility in Daphnia magna.The test item was corrected for the solid fraction and added to the medium at nominal concentrations of 11, 24, 52.9, 116.2 and 255.4 mg test item/L (corresponding to 4.3, 9.4, 20.7, 45.5 and 100 mg solids/L). Twenty daphnia per concentration and a blank control, divided over four vessels, were exposed to the test solutions for 48 hours. The number of immobilised daphnids after 24 hours and 48 hours was recorded. Duplicate samples for analysis were taken at t=0 and t=48 to determine actual exposure concentrations. Analysis showed that the test concentrations remained 84-100% of nominal test concentrations and thus the effect concentrations were based on nominal test concentrations.

In the lowest concentrations (11 and 24 mg/L) no daphnids became immobilised, while in the highest concentration all daphnids became immobilised. The 48h-EC50 of Miranol Ultra C32 was determined to be 64.8 mg/L (25.4 mg solids/L) with 95% confidence interval 52.7 -79.6 mg/L (20.6 -31.2 mg solids/L). All validity criteria were met and the study was considered to be valid.

Description of key information

Two recent studies with the registered substance (mono-acetate form and di-acetate form) are available, as well as 8 older studies (seven Klimish 2 studies, reliable with restrictions, and one Klimish 1 study, reliable without restriction). The EC50 values for the registered substance are 25.4 mg solids/L and 56.7 mg solids/L. Comparing the older data with the results of the daphnia studies performed in 2017 show that the newer studies give a higher EC50 value. This is expected to be related to the degree of purity of the substances tested. However, the results from the recent acute studies with daphnids are considered more relevant and reliable than the older reported EC50 values. See the read-across report in Section 13 for full details of the read-across rationale. The lowest EC50 value obtained with the registered substance (25.4 mg/L based on solid content, for the mono-acetate form) is used as a worst-case key value for chemical safety assessment.

Key value for chemical safety assessment

Fresh water invertebrates

Fresh water invertebrates
Effect concentration:
25.4 mg/L

Additional information

C8 -C18 mono-acetate:

EC50: 25.4 mg/L; NOEC 9.4 mg/L

C8 -C18 di-acetate:

EC50: 56.7 mg/L; NOEC 20.7 mg/L