Relative genotoxic activities of pesticides evaluated by a modified SOS microplate assay.

The genotoxic activities of 47 pesticides were determined using a modified SOS microplate assay in which the induction of beta-galactosidase in E. coli PQ37 was used as a quantitative measure of genotoxic activity. The results were compared with those obtained with anethole, curcumin, and capsaicin, a few examples of naturally occurring compounds present in foods. The assays were conducted with pesticides dissolved either in a suitable solvent, such as 10% DMSO in physiological saline or dispersed in sodium taurocholate micelles, to simulate conditions in the small intestine from where these substances are normally absorbed from the diet. 4-Nitroquinoline oxide (4-NQO) served as the reference standard of a direct acting mutagen. In micellar form, 4-NQO and 25 of the 47 pesticides tested showed significantly higher genotoxic activities than when they were tested in an organic solvent. In micellar form the SOS inducing potency of 4-NQO was almost twice as high as in 10% DMSO in physiological saline. In taurocholate micelles, the five most active compounds had activities in the range of 1,234-3,765 units/mumol and in the order of decreasing activities they were ranked as follows: malathion > dichlorvos > lindane > chlordane > endrin. They were significantly less active than 4-NQO (less than 40%). In micellar solution the naturally occurring compounds, anethole, curcumin, and capsaicin gave activities of 4,594, 928, and 809 units/mumol, respectively. These studies show that genotoxicity may depend upon the environment in which cells are exposed to these potential genotoxins. It appears that testing of the more hydrophobic compounds, both synthetic and naturally occurring, are needed.

Quantitative assessment of groundwater quality using a biological indicator: some preliminary observations.

The genotoxicity of groundwater was evaluated, using a novel application of the SOS microplate assay (SOSMA). Organic residues were extracted from groundwater samples from Maryland, Pennsylvania, and Delaware by using C-18 bonded silica solid phase extraction tubes. Total organic carbon content (TOC) of water samples was also determined. The genotoxicity of the extracts was determined by the SOSMA. Relative activity (RA) as determined by the SOSMA is a quantitative measure of genotoxicity based on a comparison to the activity of the mutagen, 4-nitroquinoline oxide. Low levels of RA (about 2x background) were detected in waters from sites within these states. There was considerable temporal and spatial variation in the observed RA, but no definite patterns were observed in the variation. Between sampling sites there was a positive correlation between RA and TOC; however, this relationship appeared to be reversed occasionally within a sampling site. The extraction and bioassay methods provide an easy and relatively inexpensive means of determining water quality.

Solid-phase extraction of pesticides from water: possible interferences from dissolved organic material.

A multiresidue analysis for trifluralin, simazine, atrazine, propazine, diazinon, parathion-methyl, alachlor, malathion, parathion, chlorpyrifos, pendimethalin, methidathion, and DEF in water that utilizes liquid-solid extraction (LSE) with octadecyl-bonded silica cartridges (C18BSCs) followed by gas chromatography/mass spectrometric analysis was developed. Recoveries of most pesticides were greater than 80% with C18BSCs from fortified water at concentration levels from about 1 to 500 ppb. Recoveries with C18BSCs, from an optically adjusted humic acid solution (10 ppm dissolved organic carbon) made to simulate a natural water with a high dissolved organic content, ranged from 29 to 153% and in general were lower than recoveries obtained from pure water. 14C-Labeled diazinon and parathion were recovered from the humic acid solution at levels of 57 and 68%, respectively, with C18BSCs; the remainder of the labeled pesticides was found in the cartridge eluents. Partition coefficients with human acid were calculated based on recovery of 14C-labeled pesticides from the C18BSCs.

Pesticide loss to the atmosphere.

Pesticides may be transformed by chemical and biological processes or transported from the site of application by several processes including runoff, movement through the soil to ground water, volatilization, transport on soil particles, and wind erosion. Contamination of water by pesticide residues is a matter of concern as is contamination of the earth's atmosphere. The form in which a pesticide enters the air and the dimensions of pesticide-containing particulate matter affect movement and deposition. Local transport over distances of several miles may be responsible for adverse effects on nontarget species. Effects of long-range transport are more difficult to assess, but pesticides increase the burden of organic chemicals in the atmosphere. Field measurements of pesticide volatilization and deposition of residues in rainfall, particulate matter, fog, etc., provide information on the relative importance of these processes. Adequate information concerning chemical reactions of pesticides in air is lacking. Because it is desirable to minimize low-level human and environmental exposure resulting from airborne pesticide residues, potential for losses to the air should be taken into account in selecting pesticide formulations and application methods.

An unusual lepidopteran sex pheromone system in the bagworm moth.

The female sex pheromone of the bagworm moth is (R)-1-methylbutyl decanoate. The antipode is biologically inactive and it neither enhances nor detracts from the potency of the R enantiomer. Unlike other moths for which female pheromones have been identified, the female secretes the pheromone from glands on her thorax and it is disseminated from hair that is shed from her body.

Isolation, identification, synthesis, and bioassay of the pheromone of the comstock mealybug and some analogs.

The sex pheromone of the Comstock mealybug,Pseudococcus comstocki (Kuwana) was isolated from volatiles trapped from air passing over virgin female insects. Combined gas chromatography, mass and infrared spectroscopy, and microreactions indicated that the structure was 2,6-dimethyl-1,5-heptadien-3-ol acetate. This was confirmed by synthesis; several analogs were also prepared. The natural and synthetic pheromone caused similar trap capture of male insects. Synthetic analogs were significantly less attractive in field tests and the addition of minor amounts of the corresponding alcohol to the pheromone appeared to enhance trap capture, but the results were not statistically conclusive.

Air permeation tests with (Z,Z)-3,13-octadecadien-1-ol acetate for reduction in trap catch of peachtree and lesser peachtree borer moths.

Air permeation trials were conducted to determine whether trap catches of the peachtree borer (PTB)Synanthedon exitiosa (Say) and lesser peachtree borer (LPTB)S. pictipes (Grote and Robinson) could be reduced through application of the synthetic pheromone of the PTB, (Z,Z)-3,13-octadecadien-1-ol acetate (Z,Z-ODDA), at 92% isomeric purity. The pheromone was released into the air of peach orchard test plots with hanging laminated plastic dispensers or hollow fiber dispensers in the trees and by aerial dispersal of microcapsules containing a solution of the lure. Results showed that all formulations ofZ, Z-ODDA reduced trap catches of both PTB and LPTB in treated plots relative to catches in traps in untreated plots. In one air permeation experiment, three types of laminated dispensers and one type of hollow fiber dispenser each reduced trap catch of PTB by 93-100% and of LPTB by 75-95%. In a separate test, two formulations of microencapsulatedZ,Z-ODDA did not reduce trap catch of male PTB as effectively as the laminated dispenser; results for LPTB were similar for both the dispensers and microcapsules. Catches of male PTB moths in traps baited with laminated and or fiber pheromone dispensers containing ODDA (94∶6%Z,Z∶E,Z) were not significantly different. LPTB male moths were also captured in these traps, the catches being dependent upon the initial pheromone loading and the type of dispensers.

Trace chemicals: the essence of sexual communication systems in heliothis species.

Analysis of heptane-soluble compounds from ovipositors of Heliothis zea and Heliothis virescens shows that both species produce relatively large amounts of (Z)-11-hexadecenal, with traces of (Z)-9-hexadecenal, (Z)-7-hexadecenal, and hexadecanal. Heliothis virescens females differ from Heliothis zea in that they also produce trace amounts of tetradecanal, (Z)-9-tetradecenal, and (Z)-11-hexadecen-1-ol. In both species, trace compounds are essential to pheromonal activity and specificity of chemical signals.