S-metolachlor pulse exposure on the alga Scenedesmus vacuolatus: Effects during exposure and the subsequent recovery

Chemosphere

Volumn 73, Issue 3, 2008, Pages 395-400

  Vallotton, Nathalie ^a   Moser, Daya ^a   Eggen, Rik I L ^a   Junghans, Marion ^a   Chèvre, Nathalie ^b  

^a SWISS FEDERAL INSTITUTE OF AQUATIC SCIENCE AND TECHNOLOGY   (Switzerland)

^b UNIVERSITY OF LAUSANNE   (Switzerland)

Author keywords

Algae; Chloroacetanilide; Herbicide; Peak exposure

Indexed keywords

AGRICULTURAL ENGINEERING; ALGAE; PEST CONTROL; PESTICIDES; PHYTOPLANKTON; WEED CONTROL;

CHLOROACETANILIDE; DEVELOPMENT STAGES; HERBICIDE; METOLACHLOR; PEAK CONCENTRATIONS; PEAK EXPOSURE; PULSE EXPOSURE; RAIN EVENTS; SCENEDESMUS VACUOLATUS;

HERBICIDES;

HERBICIDE; METOLACHLOR;

BIOLOGICAL DEVELOPMENT; CONCENTRATION (COMPOSITION); GREEN ALGA; GROWTH RATE; GROWTH RESPONSE; HERBICIDE; INHIBITION; MEASUREMENT METHOD; POLLUTION EXPOSURE;

ALGAL GROWTH; ARTICLE; CELL DIVISION; CELL GROWTH; CELL MATURATION; CELL SIZE; DEVELOPMENTAL STAGE; GROWTH INHIBITION; GROWTH RATE; NONHUMAN; SCENEDESMUS;

ACETAMIDES; SCENEDESMUS; WATER POLLUTANTS, CHEMICAL;

ALGAE; SCENEDESMUS VACUOLATUS;

EID: 50049124727     PISSN: 00456535     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2008.05.039     Document Type: Article

References (34)

1. Altenburger R., Bodeker W., Faust M., and Grimme L.H. Evaluation of the isobologram method for the assessment of mixtures of chemicals - combination effect studies with pesticides in algal biotests. Ecotoxicol. Environ. Saf. 20 (1990) 98-114
2. Atkinson A.W., John P.C.L., and Gunning B.E.S. Sporopollenin in cell-wall of chlorella and other algae - ultrastructure, chemistry, and incorporation of C-14-acetate, studied in synchronous cultures. Planta 107 (1972) 1-32
3. Balsiger, C., Niederhauser, P., Jäggi, O., Meier, W., 2004. Pestizide in Fliessgewässern des Kantons Zürich - Auswertung der Untersuchungen von 1999 bis 2003. Amt für Abfall, Wasser, Energie und Luft (AWEL), Zurich, Switzerland.
4. Battaglin W.A., Furlong E.T., Burkhardt M.R., and Peter C.J. Occurrence of sulfonylurea, sulfonamide, imidazolinone, and other herbicides in rivers, reservoirs and ground water in the Midwestern United States, 1998. Sci. Total Environ. 248 (2000) 123-133
5. Böger P. Mode of action for chloroacetamides and functionally related compounds. J. Pestic. Sci. 28 (2003) 324-329
6. Buser H.R., Poiger T., and Muller M.D. Verifying the chiral switch of the pesticide metolachlor on the basis of the enantiomer composition of environmental residues. Chimia 56 (2002) 300-303
7. Cedergreen N., Andersen L., Olesen C.F., Spliid H.H., and Streibig J.C. Does the effect of herbicide pulse exposure on aquatic plants depend on K-ow or mode of action?. Aquat. Toxicol. 71 (2005) 261-271
8. Chèvre N., Loepfe C., Fenner K., Singer H., Escher B., and Stamm C. Pestizide in schweizer Oberflächengewässern: wirkungsbasierte Qualitätskriterien Gaz, Wasser. Abwasser. 4 (2006) 297-307
9. Chèvre N., Brazzale A.R., Becker-van Slooten K., Behra R., Tarradellas J., and Guettinger H. Modelling the concentration-response function of the herbicide dinoseb on Daphnia magna (survival time, reproduction) and Pseudokirchneriella subcapitata (growth rate). Ecotoxicol. Environ. Saf. 62 (2005) 17-25
10. Couderchet M., Bocion P.F., Chollet R., Seckinger K., and Boger P. Biological activity of two stereoisomers of the N-thienyl chloroacetamide herbicide dimethenamid. Pestic. Sci. 50 (1997) 221-227
11. Couderchet M., Schmalfuss J., and Boger P. Incorporation of oleic acid into sporopollenin and its inhibition by the chloroacetamide herbicide metazachlor. Pestic. Biochem. Physiol. 55 (1996) 189-199
12. Deal L.M., and Hess F.D. An analysis of the growth inhibitory characteristics of alachlor and metolachlor. Weed Sci. 28 (1980) 168-175
13. Dixon D.P., Cummins I., Cole D.J., and Edwards R. Glutathione-mediated detoxification systems in plants. Curr. Opin. Plant. Biol. 1 (1998) 258-266
14. Eckermann C., Matthes B., Nimtz M., Reiser V., Lederer B., Boger P., and Schroder J. Covalent binding of chloroacetamide herbicides to the active site cysteine of plant type III polyketide synthases. Phytochemistry 64 (2003) 1045-1054
15. Fairchild J.F., Ruessler D.S., and Carlson A.R. Comparative sensitivity of five species of macrophytes and six species of algae to atrazine, metribuzin, alachlor, and metolachlor. Environ. Toxicol. Chem. 17 (1998) 1830-1834
16. Fedtke, C., 1982. Modes of herbicide action as determined with Chlamydomonas-reinhardii and coulter counting. In: ACS Symposium Series 181, pp. 231-250.
17. Gilliom, R.J., Barbash, J.E., Crawford, C.G., Hamilton, P.A., Martin, J.D., Nakagaki, N., Nowell, L.H., Scott, J.C., Stackelberg, P.E., Thelin, G.P., Wolock, D.M., 2006. The Quality of Our Nation's Waters-Pesticides in the Nation's Streams and Ground Water, 1992-2001. SU.S. Geological Survey Circular 1291, USA, p. 172.
18. Götz T., and Böger P. The very-long-chain fatty acid synthase is inhibited by chloroacetamides. Z. Naturforsch.(C) 59 (2004) 549-553
19. Junghans M., Backhaus T., Faust M., Scholze M., and Grimme L.H. Predictability of combined effects of eight chloroacetanilide herbicides on algal reproduction. Pest Manag. Sci. 59 (2003) 1101-1110
20. Kessler E., Schaefer M., Huemmer C., Kloboucek A., and Huss V. Physiological, biochemical, and molecular characters of the taxonomy of the subgenera of Scenedesmus (Chlorococcales, Chlorophyta). Bot. Acta 110 (1997) 244-250
21. Konstantinou I.K., Hela D.G., and Albanis T.A. The status of pesticide pollution in surface waters (rivers and lakes) of Greece. Part I. Review on occurrence and levels. Environ. Pollut. 141 (2006) 555-570
22. Kring F., Couderchet M., and Boger P. Inhibition of oleic acid incorporation into a non-lipid fraction by chloroacetamide herbicides. Physiol. Plant. 95 (1995) 551-558
23. Le Faucheur S., Behra R., and Sigg L. Phytochelatin induction, cadmium accumulation, and algal sensitivity to free cadmium ion in Scenedesmus vacuolatus. Environ. Toxicol. Chem. 24 (2005) 1731-1737
24. Leu C. Sources, Processes and Factors Determining the Losses of Atrazine, Dimethenamid and Metolachlor to Surface Waters: a Simultaneous Assessment in six Agriculture Catchments. Eidgenössische Technische Hochschule Zürich (ETHZ) (2003), Zurich, Switzerland
25. Lewis M.A. Use of freshwater plants for phytotoxicity testing: A review. Environ. Pollut. 87 (1995) 319-336
26. Muthmann, R., Nardin, P. 2007. The Use of Plant Protection Products in the European Union: Data 1992-2003. Office for Official Publications of the European Communities, Luxembourg.
27. Ng H.Y.F., and Clegg S.B. Atrazine and metolachlor losses in runoff events from an agricultural watershed: the importance of runoff components. Sci. Total Environ. 193 (1997) 215-228
28. Schmalfuss J., Matthes B., Knuth K., and Boger P. Inhibition of acyl-CoA elongation by chloroacetamide herbicides in microsomes from leek seedlings. Pestic. Biochem. Physiol. 67 (2000) 25-35
29. Schmalfuss J., Matthes B., Mayer P., and Boger P. Chloroacetamide mode of action, I: Inhibition of very long chain fatty acid synthesis in Scenedesmus acutus. Z. Naturforsch.(C) 53 (1998) 995-1003
30. Stoob K., Singer H.P., Goetz C.W., Ruff M., and Mueller S.R. Fully automated online solid phase extraction coupled directly to liquid chromatography-tandem mass spectrometry - Quantification of sulfonamide antibiotics, neutral and acidic pesticides at low concentrations in surface waters. J. Chromatogr. A 1097 (2005) 138-147
31. Tamiya H., Iwamura T., Shibata K., Hase E., and Nihei T. Correlation between Photosynthesis and Light-Independent Metabolism in the Growth of Chlorella. Biochim. Biophys. Acta 12 (1953) 23-40
32. Vallotton N., Eggen R.I.L., Escher B.I., Krayenbuhl J., and Chevre N. Effect of pulse herbicidal exposure on Scenedesmus vacuolatus: a comparison of two photosystem II inhibitors. Environ. Toxicol. Chem. 27 (2008) 1399-1407
33. Weisshaar H., and Boger P. Primary effects of chloroacetamides. Pestic. Biochem. Physiol. 28 (1987) 286-293
34. Yamamoto M., Fujishita M., Hirata A., and Kawano S. Regeneration and maturation of daughter cell walls in the autospore-forming green alga Chlorella vulgaris (Chlorophyta, Trebouxiophyceae). J. Plant Res. 117 (2004) 257-264