Effects of an atrazine, metolachlor and fipronil mixture on Hyalella azteca (Saussure) in a modified backwater wetland.

We examined the toxicity mitigation efficiency of a hydrologically modified backwater wetland amended with a pesticide mixture of atrazine, metolachlor, and fipronil, using 96 h survival bioassays with Hyalella azteca. Significant H. azteca 96 h mortality occurred within the first 2 h of amendment at the upstream amendment site but not at any time at the downstream site. H. azteca survival varied spatially and temporally in conjunction with measured pesticide mixture concentrations. Hyalella azteca 96 h survival pesticide mixture effects concentrations ranges were 10.214­11.997, 5.822­6.658, 0.650­0.817, and 0.030­0.048 µg L−1 for atrazine, metolachlor, fipronil, and fipronil-sulfone, respectively.

Agricultural pesticides in Mississippi Delta oxbow lake sediments during autumn and their effects on Hyalella azteca.

Agricultural pesticide contamination of sediments from five Mississippi Delta oxbow lakes and their effects and bioavailablity to Hyalella azteca were assessed during a low-application season-autumn. Three reference oxbow lakes were located in the White River National Wildlife Refuge (WRNWR), Arkansas and two impaired lakes, according to the US Environmental Agency Sect. 303 (d) Clean Water Act, were located in Mississippi. Surface sediment (top 5 cm) was collected at three sites within each lake and analyzed for 17 current and historic-use pesticides and metabolites. Chronic 28-day H. azteca sediment bioassays and pesticide body residue analyses were completed to determine the degree of biological responses and bioavailability. The greatest number of detectable pesticides in WRNWR and 303 (d) sediment samples was 9 and 12, respectively, with historic-use pesticide metabolite, p,p'-DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene] ubiquitous. No significant (p > 0.05) differences in animal survival were observed among sites. Animal growth was significantly (p < 0.05) less at only one site in a 303 (d)-listed lake (Macon Lake). Only six pesticides were observed in H. azteca with current-use pesticides detected at three sites; historic-use pesticides and metabolites detected at 11 sites. Animal body residues of a historic-use pesticide (dieldrin) and metabolite (p,p'-DDE) were associated with observed growth responses. Results show limited current-use pesticide contamination of sediments and H. azteca body tissues during autumn and that historic-use pesticides and metabolites are the primary contributors to observed biological responses.

Characterization and plant expression of a glyphosate-tolerant enolpyruvylshikimate phosphate synthase.

BACKGROUND: Glyphosate tolerance is a dominant trait in modern biotech crops. RESULTS: A gene encoding a glyphosate-tolerant EPSP synthase (aroA(1398)) from bacterial strain ATX1398 was cloned and characterized. The protein is initiated at a GTG translational start codon to produce a protein that provides robust glyphosate resistance in Escherichia coli (Mig) Cast & Chalm. The aroA(1398) protein was expressed and purified from E. coli, and key kinetic values were determined (K(i) = 161 microM; K(m)(PEP) = 11.3 microM; k(cat) = 28.3 s(-1)). The full-length enzyme is 800-fold more resistant to glyphosate than the maize EPSP synthase while retaining high affinity for the substrate phosphoenol pyruvate. To evaluate further the potential of aroA(1398), transgenic maize events expressing the aroA(1398) protein were generated. T(0) plants were screened for tolerance to glyphosate sprays at 1.3x commercial spray rates, and T(1) plants were selected that completely resisted glyphosate sprays at 1x, 2x and 4x recommended spray rates in field trials. CONCLUSION: These data suggest that aroA(1398) is a suitable candidate for conferring glyphosate tolerance in transgenic crop plants.