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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:
2007-06-08 to 2007-06-15
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Mortality at the intermediate concentrations may be related to the physical mixture of the solvent and test article.
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
GLP compliance:
yes
Analytical monitoring:
yes
Details on sampling:
- Sampling method: Measurement of test concentrations in one replicate test chamber of each treatment group at test initiation and test termination.
Vehicle:
yes
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION

- Method: Test solutions were prepared by direct addition of the test article to dilution water (100 and 200 mg/L treatment groups) or by addition of stocks prepared in DMF (13, 25 and 50 mg/L treatment groups).  The solvent solutions were used in the lower concentration treatments in order to facilitate accurate delivery of smaller amounts of the tests substance in the diluter system. The solvent control, 13, 25 and 50 mg/L treatment groups contained 0.1 mL/L DMF.  No solvent was delivered in the 100 and 200 mg/L treatment groups.  The diluter flow rate provided 32 volume additions/day.
Test organisms (species):
Daphnia magna
Details on test organisms:
TEST ORGANISM

- Source, supplier, any pretreatment, breeding method:  Dow Corning in-house Cultures. The cultures were initiated with organisms obtained from Aquatic Biosystems Inc., Fort Collins, Colorado.      

- Age at study initiation:  <24 hours old
Test type:
flow-through
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Hardness:
Hardness 105 mg/L as CaCO3, Alkalinity 65 mg/L as CaCO3
Test temperature:
19.5 to 21.0ºC
pH:
7.5-7.8
Dissolved oxygen:
7.8-8.9 mg/L
Salinity:
Not applicable
Nominal and measured concentrations:
Nominal concentrations: Negative Control, Solvent Control, 13, 25, 50, 100 and 200 mg/L 

Mean measured concentrations:
Recoveries of methyltrimethoxysilane were low because the hydrolysis half-life is approximately 2.2 hours.

The results are reported with reference to mean measured concentrations.
Details on test conditions:
TEST SYSTEM

- Exposure vessel type:  The test compartments were 300-mL glass beakers with 2 holes on opposite sides covered with nylon screen.  The test chambers were placed in 7.5-L polyethylene aquaria containing 3.4 L of test solution.  

- Dilution water source:  Dechlorinated Municipal Water

- Dilution water chemistry (hardness, alkalinity, pH, TOC, TSS, salinity, Ca/Mg ration, Na/K ratio):  Hardness 105 mg/L as CaCO3, Alkalinity 65 mg/L as CaCO3, pH 7.6, Conductivity 319  mhos/cm and Total Residual Chlorine <10  g/L

- Lighting (quality, intensity, and periodicity):  Wavelength similar to natural sunlight, 55 to 66 foot-candles, 16 hours light:8 hours dark

- Water chemistry in test:  DO, pH and temperature measured in each test chamber daily

- Element (unit) basis (i.e., immobilization):  Mortality and immobilization

- Test design (number of replicates, individuals per replicate, concentrations):  Two replicates/treatment, 10 individuals/replicate

- Method of calculating mean measured concentrations:  Arithmetic mean.
Reference substance (positive control):
no
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 122 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
>= 122 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 200 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
>= 200 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Details on results:
- Immobilisation of control: 0
Reported statistics and error estimates:
No significant mortalities were recorded in the highest treatment. An EC50 value could therefore not be determined.

Table 1. Test results

 Nominal concentration (mg/L)  Mean measured concentration (mg/L) Percentage immobilisation after 24 hours   Percentage immobilisation after 48 hours 
 0 (Control)  -  0  0
 0 (Vehicle control)  -  0  0
 13  6  0  0
 25  15  0  35
 50  31  0  75
 100  56  0  0
 200  122  0  0

Was control response satisfactory: Yes

The effects observed in the 15 and 31 mg/L treatments were thought to relate to physical interaction with the test substance and solvent.

Validity criteria fulfilled:
yes
Conclusions:
A 48-hour EC50 value of >122 mg/L and NOEC of ≥122 mg/L have been determined for the effects of the substance on mobility of Daphnia magna. Under the flow-through conditions used in the test the results reflect exposure to the test substance.

Description of key information

Short-term toxicity to aquatic invertebrates: 48-hour EC50 >122 mg/l (measured concentration), mobility of Daphnia magna.

Key value for chemical safety assessment

Additional information

A 48-hour EC50 value of >200 mg/l, based on nominal concentration (highest concentration tested), and >122 mg/l, based on measured concentration, has been determined for the effects of the registered substance on mobility of Daphnia magna (Dow Corning Corporation 2007). The test was carried out in accordance with test guideline OECD 202 and in compliance with GLP. Under the flow-through conditions used in the test it is likely that the Daphnia were exposed to a mixture of the parent substance and its hydrolysis products. This is reflected in the nominal versus measured test concentrations.

To support the chemical safety assessment of the hydrolysis product, methylsilanetriol (CAS 2445-53-6; EC No. 219-489-9), data have been read-across from a structural analogue which rapidly hydrolyses to methylsilanetriol. A 96-hour EC50 value of >500 mg/l (nominal concentration) (highest concentration tested) has been determined for the effects of triethoxy(methyl)silane (CAS 2031-67-6; EC No. 217-983-9) on mobility of Daphnia magna (Hazelton, 1994), carried out in accordance with EU test Method C.3 and in compliance with GLP.

In view of the test media preparation method/exposure regime it is likely that the test organisms were exposed predominantly to the hydrolysis products of the tested substance. The results may be expressed in terms of concentration of the hydrolysis product, methylsilanetriol, by applying a molecular weight correction: (MW of silanol = 94.14 / MW of parent = 178.31) * (CONCENTRATION OF PARENT = >500) = >264 mg/l as methylsilanetriol.

Refer to Section 6 endpoint summary, Section 7.0 of CSR, for further discussion of the approach to chemical safety assessment for this registration substance, and justification for read-across used.