EurekaMag.com logo
+ Site Statistics
References:
53,869,633
Abstracts:
29,686,251
+ Search Articles
+ Subscribe to Site Feeds
EurekaMag Most Shared ContentMost Shared
EurekaMag PDF Full Text ContentPDF Full Text
+ PDF Full Text
Request PDF Full TextRequest PDF Full Text
+ Follow Us
Follow on FacebookFollow on Facebook
Follow on TwitterFollow on Twitter
Follow on LinkedInFollow on LinkedIn

+ Translate

Residue dynamics and persistence of aldicarb and its biologically similar active metabolites in grapevines



Residue dynamics and persistence of aldicarb and its biologically similar active metabolites in grapevines



Journal of Nematology 13(1): 29-36



Aldicarb residues and those of its biologically similar active metabolites, aldicarb sulphoxide and aldicarb sulphone, were found in the roots, trunks, stems and leaves of grapevines 120 days after application. Residues in leaves of 1.40 and 8.89 p.p.m. resulted from applications of 4.5 and 9 kg/ha, respectively. No residues were detected in the newly forming immature fruit.

(PDF emailed within 1 workday: $29.90)

Accession: 000969596

Download citation: RISBibTeXText

PMID: 19300718



Related references

Residue dynamics and persistence of aldicarb and its biologically similar active metabolites in grapevines vitis vinifera cultivar thompson seedless. Journal of Nematology 13(1): 29-36, 1981

The residue dynamics in grapevine of aldicarb and its biologically similar active metabolites. Journal of Nematology 11: 300, 1979

Distribution and persistence of aldicarb residue in the sand-and-gravel aquifer of central Wisconsin; I, Relationship between aldicarb residue concentrations and groundwater chemistry. Pages 501-527 1988, 1988

Effects of aldicarb and its biologically active metabolites on bees. Environmental Entomology 13(5): 1386-1398, 1984

Distribution and persistence of aldicarb residues in the sand-and-gravel aquifer of central Wisconsin; 1, Relationship between aldicarb residue concentrations and groundwater chemistry. Developments in Environmental Modelling 13: 59-84, 1988

Distribution and persistence of aldicarb residues in the sand-and-gravel aquifer of central Wisconsin; 2, Simulation of aldicarb residue distributions in groundwater using a combined leaching and groundwater transport model. Developments in Environmental Modelling 13: 85-104, 1988

Aldicarb residue persistence in leaf terminals of 'Florunner' peanut. Journal of Economic Entomology 85(4): 1072-1078, 1992

Determination of nematicide aldicarb and its metabolites aldicarb sulfoxide and aldicarb sulfone in soils and potatoes by liquid chromatography with photodiode array detection. Journal of Liquid Chromatography 18(16): 3243-3256, 1995

Method for the gas chromatographic determination of residues of aldicarb and its toxicological important metabolites aldicarb sulfoxide and aldicarb sulfone in strawberry fruits and plants, sugarbeets, and soils. Nachrichtenblatt des Deutschen Pflanzenschutzdienstes 36(3): 36-39, 1984

Apaf-1 oligomerizes into biologically active (similar)700-kDa and inactive (similar)1.4-MDa apoptosome complexes. The Journal of Biological Chemistry 275(9): 67-70, 2000

Direct gas chromatographic determination of 2 isomeric insecticides aldicarb and butocarboxime and their toxic metabolites application to residue analysis in crops and leaves. Zeitschrift fuer Lebensmittel-Untersuchung und -Forschung 180(2): 96-100, 1985

Direct gas chromatographic determination of the two isomeric insecticides, aldicarb and butocarboxime and their toxic metabolites: application to residue analysis in crops and leaves. Zeitschrift für Lebensmittel-Untersuchung und -Forschung 180(2): 96-100, 1985

Environmental metabolites of fluoroquinolones: synthesis, fractionation and toxicological assessment of some biologically active metabolites of ciprofloxacin. Environmental Science and Pollution Research International 19(7): 2697-2707, 2012

On the occurrence of biologically active metabolites of the active ingredient S 1752 after application of Lebaycid. PflSchNachr. Bayer. Leverkusen, 15: 3, 125-147, 1963

Occurrence of biologically active metabolites of the active ingredient S 1752 after application of Lebaycid. Pflanzenschutz Nachrichten Bayer" 15(3): 129-151, 1962