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1.
Arch Environ Contam Toxicol ; 52(1): 64-72, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17106792

ABSTRACT

The probabilistic ecological risk assessment-toxic equivalent (PERA-TE) combination approach is a relatively new risk assessment approach used to assess the toxicity and interaction of chemical mixtures. The validity and effectiveness of the PERA-TE combination approach has been tested previously in field microcosm studies using pesticide mixtures. The related laboratory studies described here, using Daphnia magna, were conducted to verify the conclusions made regarding the toxicity and interaction of the mixtures tested in the microcosms. Two types of pesticide mixture were assessed: the first consisted of pesticides with similar modes of action (chlorpyrifos, diazinon, and azinphos-methyl; OP mixture), and the second consisted of pesticides with different modes of action (chlorpyrifos, endosulfan, and trifluralin; CET mixture). Similar to the field studies, PERA-TE mixtures with a predetermined effect assessment criterion (10th centile of acute toxicity effects distributions) and proportional ratio (89:11 for binary mixture and 80:10:10 for ternary mixtures) were tested. Further assessment of the (PERA-) TE approach was achieved by altering the effect assessment criterion (to EC/LC(50) point estimates) and the proportional ratio of the pesticides in the mixture (to 50:25:25). Generally, but with some exceptions, basing mixtures on species-specific effect criteria and/or changing the proportional ratio of pesticides in the mixture redistributed the concentration of pesticides in the mixture to produce an equitoxic response. The ability to produce these equitoxic responses supported the conclusions drawn from the field studies: The pesticide toxicity in the OP and CET PERA-TE mixtures were effectively additive. Furthermore, it is shown that these alternative (PERA-) TE mixtures would be suitable to confirm or reject the interaction of chemicals in a PERA-TE mixture.


Subject(s)
Daphnia/drug effects , Pesticides/toxicity , Water Pollutants, Chemical/toxicity , Animals , Daphnia/physiology , Drug Combinations , Drug Interactions , Longevity/drug effects , Pesticides/analysis , Risk Assessment , Toxicity Tests , Water Pollutants, Chemical/analysis
2.
Environ Monit Assess ; 85(3): 309-26, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12841692

ABSTRACT

The presence of several anthropogenic chemicals has been documented in the atmosphere of the Canadian prairies. The deposition of these chemicals as a mixture is of importance since little is known of the combined effects of these chemicals on aquatic organisms. This study was designed to evaluate the acute and chronic toxicity of a complex mixture of nine atmospherically transported pesticides to Ceriodaphnia dubia. The nine selected pesticides (bromoxynil, dicamba, 2,4-D, MCPA, triallate, trifluralin, pentachlorophenol, lindane, and 4,4'-DDT) were detected in appreciable quantities in dry atmospheric deposits. The concentration of each pesticide in the mixture was based on maximum measured daily dry deposition rates for central Canada, except for pentachlorophenol, which was estimated based on atmospheric concentrations. The 48-h LC50 estimate for C. dubia exposed to the pesticide mixture was 174.60 microg L(-1) (340 times the measured total dry deposition concentration). The estimated NOEC and LOEC for both survival and reproduction, as determined in the 7-d chronic toxicity test, were 51.3 (100 times) and 154 microg/L(-1) (300 times), respectively. A basic risk assessment, using the toxic unit approach, suggested that the toxicity of the pesticide mixture was mainly due to 4,4'-DDT. Overall, this atmospherically transported complex mixture of pesticides appears to pose a negligible toxicological risk to non-target aquatic invertebrates such as zooplankton.


Subject(s)
Air Pollutants/toxicity , Daphnia/drug effects , Pesticides/toxicity , Water Pollution, Chemical/adverse effects , Zooplankton/drug effects , Analysis of Variance , Animals , Canada , Ecosystem , Lethal Dose 50 , Mass Spectrometry , No-Observed-Adverse-Effect Level , Reproduction/drug effects , Risk Assessment , Toxicity Tests, Chronic
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