1993
DOI: 10.1002/etc.5620120721
|View full text |Cite
|
Sign up to set email alerts
|

Quantitative structure‐activity relationships for predicting the toxicity of pesticides in aquatic systems with sediment

Abstract: The toxicity of a series of organophosphorus (OP) and carbamate insecticides was measured against the midge Chironomus riparius in aquatic systems with and without sediment. Five molecular descriptors (molecular volume, Henry's law constant, n‐octanol/water partition coefficient (Kow), molecular connectivity, and linear solvation energy) were used in regression analysis as potential predictors of insecticidal activity. The regressions were conducted for each descriptor against toxicity values for the series of… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
12
1

Year Published

1994
1994
2010
2010

Publication Types

Select...
4
2
1

Relationship

0
7

Authors

Journals

citations
Cited by 26 publications
(13 citation statements)
references
References 21 publications
0
12
1
Order By: Relevance
“…For example, methyl parathion has a log K ow of 3.3 (Fisher et al 1993) and a water solubility of 55–60 mg/l at 25°C (Verschueren 1996), and thus it could have been susceptible to loss from the water exchanges.…”
Section: Discussionmentioning
confidence: 99%
See 3 more Smart Citations
“…For example, methyl parathion has a log K ow of 3.3 (Fisher et al 1993) and a water solubility of 55–60 mg/l at 25°C (Verschueren 1996), and thus it could have been susceptible to loss from the water exchanges.…”
Section: Discussionmentioning
confidence: 99%
“…), annual use, and physicochemical parameters of the nine target pesticidesTest pesticidesType of pesticideCAS no.Annual agricultural use in California (kg) a Log K ow b Log K oc c AbamectinAvermectin insecticide71751-41-25,5904.04.0DiazinonOP insecticide33-41-5116,0003.82.3DicofolOC acaricide115-32-211,6005.03.8–3.9FenpropathrinPyrethroid insecticide39515-41-814,8006.05.6–5.7IndoxacarbOxadiazine insecticide173584-44-624,2004.53.3–3.9Methyl parathionOP insecticide298-00-016,3003.33.7OxyfluorfenPhenyl ether herbicide42874-03-3275,0004.56.2PropargiteSulfite ester acaricide2312-35-8174,0003.73.6–3.9PyraclostrobinStrobilurin fungicide175013-18-051,4004.03.8–4.2

a 2008: http://www.cdpr.approximatelygov/docs/pur/purmain.htm

b Barceló et al (1994), Hazardous Substances Data Bank 2008, Saito et al (1993), (http://chemicalland21.com/lifescience/agro/FENPROPATHRIN.htm), Environmental Monitoring Branch, Department of Pesticide Regulation (2003). DPR Pesticide, Fisher et al (1993), U.S. Department of Agriculture, Agriculture Research Service, Pesticide Properties database (

…”
mentioning
confidence: 99%
See 2 more Smart Citations
“…Once these products enter waterways, they can affect the health of aquatic species, ranging from micro organisms (DeLorenzo et al 2001) to top level consumers in the food web (Robinson 1999). The partitioning of organic compounds will affect toxicity, and the total organic carbon (TOC) content of sediments determines the binding of non-ionic lipophilic molecules (Fisher et al 1993;Ankley et al 1994;Delle Site 2001).…”
Section: Introductionmentioning
confidence: 99%