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Sediment toxicity

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Administrative data

Endpoint:
sediment toxicity: short-term
Type of information:
experimental study
Adequacy of study:
disregarded due to major methodological deficiencies
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Documentation insufficient for assessment

Data source

Reference
Reference Type:
publication
Title:
RISK ASSESSMENT OF MAGNACIDE® H HERBICIDE AT Rio COLORADO IRRIGATION CHANNELS (ARGENTINA), TIER 3: STUDIES ON NATIVE SPECIES
Author:
Venturino A, Montagna MC, Pechen de Angelo AM
Year:
2007
Bibliographic source:
Environmental Toxicology and Chemistry, Vol. 26, No. 1, pp. 177-182

Materials and methods

Principles of method if other than guideline:
acute toxicity testing
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
Magnacide H
IUPAC Name:
Magnacide H
Details on test material:
Magnacide H was provided by Baker Petrolite. The active ingredient in Magnacide H is 96.08 g/L acrolein (CAS no. 107-02-8)

Sampling and analysis

Analytical monitoring:
yes

Test organisms

Test organisms (species):
Chironomus sp.
Details on test organisms:
TEST ORGANISM
- Source: wild caught, collected at CORFO-Rio Colorado irrigation channels (Argentina)
- Age at study initiation: last instar larvae

QUARANTINE (wild caught)
no data

Study design

Study type:
laboratory study
Test type:
static
Water media type:
freshwater
Type of sediment:
not specified
Exposure duration
Duration:
24 h
Exposure phase:
total exposure duration

Test conditions

Test temperature:
20-22°C
Nominal and measured concentrations:
not reported
Details on test conditions:
TEST SYSTEM
- Test vessel:
- fill volume: 200 mL
- Aeration: constant
- Sediment volume: probably no sediment was used in the test systems (not reported)
- No. of organisms per vessel: 20
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 3

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: CharcoaI-filtered and dechlorinated tap water

OTHER TEST CONDITIONS
- Photoperiod: 16h light : 8h dark

EFFECT PARAMETERS MEASURED:
Mortality

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
2.83 mg/L
Nominal / measured:
meas. (initial)
Conc. based on:
act. ingr.
Basis for effect:
mortality
Remarks on result:
other: 95% CL: 2.67-2.99 mg/L
Duration:
24 h
Dose descriptor:
other: LC95
Effect conc.:
4.19 mg/L
Nominal / measured:
meas. (initial)
Conc. based on:
act. ingr.
Basis for effect:
mortality
Remarks on result:
other: 95% CL: 3.85-4.75 mg/L
Details on results:
24h-NOEC = 1.0 mg/L
24h-LOEC = 1.62 mg/L
NOEC and LOEC values assessed experimentally, statistically different from control
Reported statistics and error estimates:
Mortality data based on the actual initial concentrations were subjected to probit analysis using a BASIC program to determine the LC50 and LC95. No-observed lethal concentration (NOEC) and lowest-observed lethal concentration (LOEC) were experimentally assessed from data and statisticaI comparison of the observed mortality versus control mortality.

Applicant's summary and conclusion

Conclusions:
Reliability not assassable due to lacks in documentation (e.g. sediment used?)