Ppm Chlorpyrifos Research Articles

Microbe-pesticide interactions: Soil enzyme analysis and bacterial degradation of chlorpyrifos

With the objective of understanding microbe—pesticide interactions in soil, the effect of pesticides alone and in combination on the activities of amylase, cellulase, and invertase was assessed in black, and red soils collected from the groundnut (Arachis hypogaea L.) cultivated fields of Andhra Pradesh, India. In addition, the potential bacteria that can break down chlorpyrifos was identified using biochemical assays and a partial 16S rRNA gene sequence analysis. Soil enzymes were analyzed using standard procedures described elsewhere. The activities of amylase, cellulase, and invertase were solely dependent on the dose of pesticides used in the current study. Enzyme activities were significantly increased at the level of 2.5 or 5.0 kg ha–1, whereas increases in the concentration of pesticides at 7.5–10 kg ha−1 were lethal to the enzyme activities in both soils at 10-day incubation. The effective combination for the increase in the activities of amylase, cellulase, and invertase were monocrotophos + mancozeb. Mineral salts medium with 50 ppm chlorpyrifos as a carbon source had the greatest growth of the bacteria (i.e. Pseudomonas citronellolis strain CF3) at 14th h of incubation with OD value of 0.24 at 660 nm, and the same strain could eliminate 75% of the chlorpyrifos within 24 h from the medium. Based on the present study it was concluded that insecticides used alone or in combination with fungicides at specific doses (2.5 or 5.0 kg ha−1) improved the amylase, cellulase, and invertase activities, which are involved in the carbon cycle in soils. Pseudomonas citronellolis strain CF3 is a potential bacterium in the remediation of chlorpyrifos-contaminated sites.

Effect of Chlorpyrifos Insecticide On The Ossification of Wader Pari Fish Vertebrae (Rasbora Lateristriata Bleeker, 1854)

Due to high growth, chlorpyrifos was one of the solution to increase food production. However, this compound is dangerous because it belongs to organophosphate group which blocking the activity of acetylcholinesterase (ache) enzyme and caused nervouse failure to animal. Due to heavy rain this insecticide will run-off and contaminate the body of the river and effect the aquatic live. Wader pari was non-target animal of chlorpyrifos. The purpose of this study was to determine the effect of chlorpyrifos exposure on the behaviour of wader's feeding and swimming response, as well as the morphology and ossification process of the vertebrae. The study was conducted for 7 days.  4 groups of fish were exposed to chlorpyrifos with concentrations of 0, 0.001, 0.005 and 0.01 ppm. Observation of the ossification and morphological process of vertebrae is carried out using AR-Ab bone staining. Observation of wader’s behaviours is carried out using descriptive analysis. It was found that the fish which exposed to chlorpyrifos showed some behavioural abnormalities in swimming and feeding response. Fish exposed to 0.005 ppm chlorpyrifos showed vertebral abnormalities which is haemal kyphosis. Kyphosis refers to Λ-shaped vertebral curvature Fragkoulis et.al, (2019). However, the ossification process that represented by Ar-Ab staining are going well.Â

Adsorptive decontamination of organophosphate pesticide chlorpyrifos from aqueous systems using bagasse-derived biochar alginate beads: Thermodynamic, equilibrium, and kinetic studies

Removal of emerging contaminants such as pesticides from aqueous systems is of growing concern. The usage of sustainable materials as adsorbents is an eco-friendly approach to water purification. Sugarcane bagasse is an abundant waste material that can serve as a sustainable source for preparing adsorbents. This work investigated the removal of chlorpyrifos from aqueous systems using a composite adsorbent prepared from sugarcane bagasse-derived biochar and encapsulated in alginate. The batch studies were conducted to examine the effect of contact time, initial pH, initial concentration of adsorbate, sorbent dosage and temperature on the extent of chlorpyrifos removal by biochar alginate beads. Adsorption thermodynamics, equilibrium isotherms, and kinetics were studied to elucidate the chlorpyrifos uptake phenomenon. The error functions were used to determine model parameters using non-linear regression approach. Biochar alginate beads showed 86 % chlorpyrifos removal under optimized conditions. The adsorption capacity was found to be 6.25 mg g−1 for pH 10 at 10 ppm chlorpyrifos concentration. The analysis of experimental isotherm data revealed Freundlich isotherm model to be the best fitting with regression coefficient value of 0.9332 Kinetic studies showed that adsorption followed intraparticle diffusion model with R2 value of 0.9750, where Boyd model was further studied to confirm rate constant. Adsorption of chlorpyrifos onto biochar beads is showed to be exothermic with type of adsorption to be physisorption.

Organophosphorus pesticide tolerance of transgenic Arabidopsis thaliana by bacterial ophB gene encode organophosphorus hydrolase

Organophosphate hydrolase (OphB) gene from Pseudomonas sp. was transferred into Arabidopsis plants to observe the bioremediation ability and tolerance level of the transgenic plant to organophosphate pesticides contaminants. Gene transfer was observed by PCR of the transgenic Arabidopsis plants’ genomic DNA. Expression of ophB gene and protein levels in the transgenic Arabidopsis plants was observed by western blot analysis. The transgenic plants were resistant and tolerant to chlorpyrifos (an organophosphate pesticide), as evidenced by a toxicity test, where the transgenic plants produced greater shoot and root biomass than that of wild type plants. The fresh weight of transgenic Arabidopsis plants’ did not reduced significantly till 400 ppm chlorpyrifos treatment, but fresh weight of wild type Arabidopsis plants’ significantly reduced by the application of 100 ppm chlorpyrifos. Moreover, in 600 ppm chlorpyrifos liquid culture, transgenic Arabidopsis plants’ produced 1.34 g biomass from 100 seeds, but wild type Arabidopsis plants’ produced only 0.24 g biomass from 100 seeds. This study indicates that transgenic Arabidopsis plants having ophB gene increase the tolerance level of organophosphate pesticides.

Biodegradation of chlorpyrifos by an optimized Bacillus consortium isolated from pesticide-contaminated soils of Kerala, India

The current study attempted to develop a bacterial consortium which can degrade chlorpyrifos pesticide efficiently. Five morphologically different bacterial strains, capable to tolerate high chlorpyrifos concentration, were isolated from pesticide-contaminated soil. Further, possible combinations of the isolates were formed and each combination was screened and chlorpyrifos degradation percentage and half-lives were calculated. The consortium CON11, comprising of four isolates (CP28, CP30, CP31, and CP34) showed the highest chlorpyrifos degradation. The individual independent variables of chlorpyrifos degradation by CON11 viz. temperature (°C), pH, incubation time (days) and pesticide concentration (ppm) were optimized using one-factor at-a-time experiments. The consortium isolates were then identified by the molecular tools 16S rRNA gene typing and the sequences were submitted to GenBank. The four bacterial isolates thus identified are Bacillus amyloliquefaciens CP28 (MH667455), Bacillus pumilus CP30 (MH667456), Bacillus marisflavi CP31 (MN715880), and Bacillus subtilis CP34 (MH667458). These isolates which comprise CON11 consortium could degrade 91% of 100 ppm chlorpyrifos after 6 days of incubation at 30 °C and pH 7 with a half-life of 1.73 days indicating the promising potential of the consortium, CON11, in the cleanup of chlorpyrifos contaminated sites.

Investigation of photocatalytic chlorpyrifos degradation by a new silica mesoporous material immobilized by WS2 and Fe3O4 nanoparticles: Application of response surface methodology

In the present research, Fe3O4 and WS2 nanoparticles immobilized on or in KIT‐6 (KIT: Korea Institute of Science and Technology) pores (KIT‐6/WS2‐Fe3O4) were synthesized and studied as a photocatalyst for degradation of representative chlorpyrifos as an organophosphorus pesticide. In addition, the KIT‐6/WS2‐Fe3O4 photocatalyst was characterized by different methods such as TEM, FESEM‐EDS‐Mapping, XRD, and N2 adsorption/desorption surface area, in order to understand their morphology, structural, and physical properties. The photocatalytic performance of this photocatalyst was investigated for degradation of chlorpyrifos by visible light irritation. The effects of variables such as chlorpyrifos concentration, KIT‐6/WS2‐Fe3O4 nanocatalyst amount, pH, and irradiation time on chlorpyrifos degradation efficiency was studied by central composite design with response surface methodology. The optimum conditions for CP degradation were obtained by 50 mg KIT‐6/WS2‐Fe3O4 nanocatalyst, and 7.2 ppm chlorpyrifos solution with pH = 6, at 52 min. The pseudo‐first‐order model with rate constants equal to 0.069 min−1 as best choice efficiency described the chlorpyrifos degradation process according to Langmuir‐Hinshelwood kinetic.

Synergistic effect and field control efficacy of the binary mixture of permethrin and chlorpyrifos to brown planthopper (Nilaparvata lugens)

Abstract The brown Planthopper (BPH), Nilaparvata lugens is a major pest of rice production in tropical Asia. The appearance of insecticide resistance challenges the control of BPH in field. The development of new insecticide is expensive and time-consuming. Thus, the precise and proper use of existing compounds becomes an important issue in resistance management of this pest. In this study, five commercial insecticides of BPH (permethrin, chlorpyrifos, imidacloprid, clothianidin and thiamethoxam) were tested to explore the toxicity of the binary mixture between different kinds of insecticides. In all combinations of mixture, the mixtures of permethrin and chlorpyrifos displays synergistic effect at three different mixture ratios (1:1, 1:10 and 10:1). The strongest synergism observed in permethrin/ chlorpyrifos mixtures at 1:1 ratio (Combination index, CI = 0.39). Addition of enzyme inhibitor followed by detoxification enzyme activity assays suggested that the mechanism of synergistic effect of permethrin/chlorpyrifos mixture may result from inhibition of the cytochrome P450 monooxygenase and esterase activity. This inference can be supported through two lines of evidence. One is decrease of toxicity when permethrin/chlorpyrifos mixture in a 1:1 ratio plus triphenyl phosphate (TPP) or piperonyl butoxide (PBO), but increase of toxicity when permethrin/chlorpyrifos mixture in a 10:1 ratio plus TPP or PBO. Another is exposure of the 3rd instar nymphs to permethrin/chlorpyrifos mixture after 72 h also significantly decreased both cytochrome P450 monooxygenases and esterase activity. Further field trail showed the mixture of 50 ppm permethrin +50 ppm chlorpyrifos increased the field control efficiency significantly rather than permethrin alone or chlorpyrifos alone. Our study indicated that the mixture of permethrin and chlorpyrifos in a 1:1 ratio might be an effective method for the control of BPH in paddy field.

Ultrastructural Effects of Chlorpyrifos and Phenthoate on the Midgut of Chrysomya albiceps Larvae (Diptera: Calliphoridae)

The Ultrastructural effects of chlorpyrifos and phenthoate on midgut of third larval instar of Chrysomya albiceps was illustrated with the aid of transmission electron microscope. It was clear that chlorpyrifos considered to be most potent than phenthoate. The number of pupae and emerged adults were reduced after treatments with all concentrations of the two insecticides. There was a predominance of males over female (ratio, 4.5:1), respectively after treatment with 15 ppm chlorpyrifos. Based on ultrastructural changes, after treatment with phenthoate, densely compressed cells with irregular shrank nucleus that has fragmented nucleoli and lacked condensed chromatin were observed in the midgut cells. The rough endoplasmic reticulum becomes swallowed. The microvilli clumped and shrunk. After treatment with chlorpyrifos, Numerous number of large vacuoles observed at the periphery of the midgut cells. The mitochondria show different degrees of deformation from clumping of cristae to rupture of mitochondrial membrane. The cells of midgut possessing short, shrunk or atrophied microvilli. Lysis of most cellular organelles is the most characteristic features after chlorpyrifos treatments.

Interactive effect of climate factors, biochar and insecticide chlorpyrifos on methane consumption and microbial abundance in a tropical Vertisol

Climate change may increase the pest infestation leading to intensive use of insecticides. However, the effect of insecticide and climate factors on soil methane (CH4) consumption is less understood. A laboratory experiment was carried out to evaluate the effect of temperature (15 °C, 35 °C, and 45 °C), moisture holding capacity (MHC) (60%, 100%), biochar (0%, 1%) and chlorpyrifos (0 ppm, 10 ppm) on CH4 consumption and microbial abundance in a tropical Vertisol of central India. Methane consumption rate k (ng CH4 consumed g−1 soil d−1) varied from 0.065 ± 0.005 to 0.608 ± 0.018. Lowest k was in 15 °C-60% moisture holding capacity (MHC)-no biochar and with 10 ppm chlorpyrifos. Highest k was in 35 °C-100% MHC-1% biochar and without (0 ppm) chlorpyrifos. Cumulative CO2 production (ng CO2 produced g−1 soil d−1) varied from 446 ± 15 to 1989 ± 116. Both CH4 consumption and CO2 production peaked in the treatment of 35 °C-100% MHC-1% biochar. Chlorpyrifos inhibited CH4 consumption irrespective of treatments. Abundance of 16S rRNA of eubacteria (× 106 g−1 soil) varied from 2.33 ± 0.58 to 85.67 ± 7.00. Abundance of 16S rRNA genes representing Actinomycetes (× 104 g−1 soil) varied from 7.67 ± 1.53 and pmoA gene (Methanotrophs) (× 105 g−1 soil) varied from 1.23 ± 0.59 to 34.33 ± 6.51. Chlorpyrifos inhibited abundance of heterotrophic bacteria and methanotrophs but stimulated actinomycetes. Biochar stimulated the CH4 consumption, CO2 production and microbial abundance. Study highlighted that use of chlorpyrifos under climate change factors may inhibit CH4 consumption but the use of biochar may alleviate the negative effect of the chlorpyrifos.

Toxicological Effects of Differently Polluted Dam Waters Spiked with Pesticides on Freshwater Snails Lymnaea Natalensis

<p>Pesticides extensively used in agricultural fields to ensure high quality crop yields indirectly find their way to aquatic bodies where they affect aquatic biota. We investigated the effects of pesticides in different dam waters on esterase enzyme activity of the freshwater snail species<em> Lymnaea natalensis</em>. Groups of adult snails were exposed to 0.006 ppm chlorpyrifos and 0.003 ppm aldicarb in polluted water from Umguza dam and relatively pristine water from Hillside dam for 14 days. Carboxylesterase, acetylcholinesterase and arylesterase activities were measured. Both pesticides caused significant inhibition of esterase activity after the 14 day exposure period, with exposures to Umguza dam water showing higher inhibition as compared to exposures to Hillside dam water. Aldicarb and chlorpyrifos both showed a time-dependent inhibition of enzyme activity, the former causing a higher inhibitory effect as compared to the latter. Acetylcholinesterase was inhibited up to 80% following exposure to aldicarb while exposure to chlorpyrifos in Umguza water caused only 40% inhibition. Carboxylesterases were similarly inhibited with higher inhibition observed in snails exposed to Umguza dam water when compared to snails exposed to Hillside dam water, while arylesterases were inhibited in the range 80-90%, with an exception of chlorpyrifos spiked Hillside dam water which caused 45% inhibition. Contaminated Umguza dam water also appeared to enhance the effects of pesticides when compared to the relatively pristine Hillside dam water. Alteration of esterase activity can be used as an early warning signal indicating exposure to environmental pollutants. The results of this study therefore, highlight the adverse effects of pesticides on non-target aquatic organisms, evidenced by the inhibition of esterase activity.</p>

Physiological, biochemical and growth responses of Azolla pinnata to chlorpyrifos and cypermethrin pesticides exposure: a comparative study

Cypermethrin and chlorpyrifos pesticide- (5, 15 and 30 ppm) induced effects on growth, metabolic and antioxidative behaviour of Azolla pinnata were analysed after 96 h of treatment. Growth of A. pinnata was increased by 72–76% over the initial mass under control condition. Further, the growth was decreased by 26 and 30% following treatment with 5 ppm of cypermethrin and chlorpyrifos, respectively, compared to control. Whereas, 30 ppm of pesticide treatment caused substantial decrease in biomass accumulation, even less than the initial mass. The Chlorophyll a content was declined at higher concentrations of chlorpyrifos, while carotenoids content increased significantly in the presence of both the pesticides. Photosynthetic rate showed declining trend with rising concentration of pesticides, while an increasing trend was noticed in the case of respiratory O2 consumption. The oxidative biomarkers malondialdehyde, superoxide radicals and hydrogen peroxide increased with increasing concentration of both the pesticides. The activity of enzymatic antioxidants enzyme superoxide dismutase, glutathione-S-transferase and ascorbate peroxidase (APX) was enhanced with increasing concentrations of both the pesticides; however, a declining trend was noticed in the case of APX at 30 ppm chlorpyrifos treatment. The study concludes that chlorpyrifos appeared to be more toxic than cypermethrin; however, both the pesticides significantly reduced the growth performance.

Understanding the Degradation Pathway of the Pesticide, Chlorpyrifos by Noble Metal Nanoparticles

Application of nanoparticles (NPs) in environmental remediation such as water purification requires a detailed understanding of the mechanistic aspects of the interaction between the species involved. Here, an attempt was made to understand the chemistry of noble metal nanoparticle-pesticide interaction, as these nanosystems are being used extensively for water purification. Our model pesticide, chlorpyrifos (CP), belonging to the organophosphorothioate group, is shown to decompose to 3,5,6-trichloro-2-pyridinol (TCP) and diethyl thiophosphate at room temperature over Ag and Au NPs, in supported and unsupported forms. The degradation products were characterized by absorption spectroscopy and electrospray ionization mass spectrometry (ESI MS). These were further confirmed by ESI tandem mass spectrometry. The interaction of CP with NP surfaces was investigated using transmission electron microscopy, energy dispersive analysis of X-rays, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). XPS reveals no change in the oxidation state of silver after the degradation of CP. It is proposed that the degradation of CP proceeds through the formation of AgNP-S surface complex, which is confirmed by Raman spectroscopy. In this complex, the P-O bond cleaves to yield a stable aromatic species, TCP. The rate of degradation of CP increases with increase of temperature and pH. Complete degradation of 10 mL of 2 ppm CP solution is achieved in 3 h using 100 mg of supported Ag@citrate NPs on neutral alumina at room temperature at a loading of ∼0.5 wt %. The effect of alumina and monolayer protection of NPs on the degradation of CP is also investigated. The rate of degradation of CP by Ag NPs is greater than that of Au NPs. The results have implications to the application of noble metal NPs for drinking water purification, as pesticide contamination is prevalent in many parts of the world. Study shows that supported Ag and Au NPs may be employed in sustainable environmental remediation, as they can be used at room temperature in aqueous solutions without the use of additional stimulus such as UV light.

Effect of dietary vanaspati alone and in combination with stressors on sero-biochemical profile and immunity in white leghorn layers

A total of 160 White Leghorns of 20 wk age were divided randomly into eight groups. Groups 1, 3, 4 and 5 were fed basal feed and the rest were fed 5% vanaspati supplemented feed until 42 wk of age. From 42 to 54 wk, groups 3, 4 and 5 were fed 1% ferrous sulfate, 100 ppm chlorpyrifos (CPS) and 100 ppm cadmium, respectively, along with basal feed and groups 6, 7 and 8 were fed similar stressors, respectively, along with 5% vanaspati. Groups 1 and 2 served as controls for basal feed and 5% vanaspati feed. Alkaline phosphatase (ALP), alanine transaminase (ALT), total protein, albumin, globulin, A/G ratio, total cholesterol, high density cholesterol (HDL), triglycerides, creatinine, hemagglutination inhibition (HI) titer, and phytohemagglutination (PHA) index were studied. Supplementation of vanaspati resulted in a significant reduction in PHA, cholesterol, albumin and HI titer. Cadmium significantly increased ALP, AST, creatinine and paradoxically increased HDL cholesterol and HI titers. Vanaspati along with cadmium showed similar effects. Administration of CPS lowered PHA index, whereas supplementation along with vanaspati decreased the HI titers and increased the PHA index. Supplementation of vanaspati alone and in combination revealed harmful effects and aggravated the toxicities of CPS and cadmium. Hence, it is concluded that consumption of vanaspati could be harmful.

Chlorpyrifos Bioassay and Resistance Monitoring of San Joaquin Valley California Citricola Scale Populations

The responses to chlorpyrifos of six populations of citricola scale, Coccus pseudomagnoliarum (Kuwana) (Hemiptera: Coccidae), were tested using a leaf dip bioassay, and two- to nine-fold resistances were found. LC50 responses of nymphs ranged from 7.5 to 68.9 ppm and LC90 responses ranged from 20 to 222 ppm chlorpyrifos. A population tested monthly during August-October showed up to 3.5-fold differences in LC50 responses but no differences in LC90 responses as scale size increased. A diagnostic concentration of 178 ppm chlorpyrifos was used to test 93 populations from throughout the San Joaquin Valley California during 2006-2009 by using a leaf dip bioassay. Of the populations tested, 41% showed > 20% survival after exposure to the diagnostic concentration of chlorpyrifos, indicating resistance problems. Research is needed to relate the level of survival of the scales in the bioassay to the field efficacy of the insecticide. Tulare County citrus growers applied a higher number of organophosphate and carbamate insecticides during the 15-yr period from 1994 to 2008, and these orchards showed a higher average scale survival of chlorpyrifos and a higher number of locations with resistant scale compared with the other San Joaquin Valley counties. Chlorpyrifos resistance is a significant issue for citricola scale management because biological control is ineffective in the San Joaquin Valley and the alternative neonicotinoid and insect growth regulator (IGR) insecticides require more frequent application.

Degradation of Chlorpyrifos by an alkaline phosphatase from the cyanobacterium Spirulina platensis

Spirulina is a photosynthetic, filamentous, spiral-shaped, multicellular, blue-green microalga. The two most important species are Spirulina maxima and Spirulina platensis. Spirulina is considered an excellent food, lacking toxicity and having corrective properties against viral attacks, anemia, tumor growth and malnutrition. We have observed that cultures of Spirulina platensis grow in media containing up to 80 ppm of the organophosphorous pesticide, Chlorpyrifos. It was found to be due to an alkaline phosphatase (ALP) activity that was detected in cell free extracts of Spirulina platensis. This activity was purified from the cell free extracts using ammonium sulphate precipitation and gel filtration and shown to belong to the class of EC 3.1.3.1 ALP. The purified enzyme degrades 100 ppm Chlorpyrifos to 20 ppm in 1 h transforming it into its primary metabolite 3, 5, 6-trichloro-2-pyridinol. This is the first report of degradation of Chlorpyrifos by Spirulina platensis whose enzymic mechanism has been clearly identified. These findings have immense potential for harnessing Spirulina platensis in bioremediation of polluted ecosystems.

Chlorpyrifos induces apoptosis in human T cells

It was found previously that organophosphorus pesticides (OPs) significantly inhibited cytotoxic T lymphocyte (CTL) activity. To explore the mechanism of OP-induced inhibition of CTL activity, the present study investigated whether OPs can induce cell death/apoptosis in T cells. Jurkat human T cells were treated with chlorpyrifos at 0–100 ppm for 2, 4, and 6 h at 37 °C in vitro. It was found that chlorpyrifos induced cell death of Jurkat human T cells in a dose- and time-dependent manner, as shown by MTT and LDH assays. Then, it was investigated if chlorpyrifos-induced cell death consisted of apoptosis, as determined by analysis of Annexin-V staining and the intracellular level of active caspase-3 by flow cytometry, and DNA fragmentation analysis. It was found that chlorpyrifos induces apoptosis in Jurkat T cells in a dose- and time-dependent manner, as determined by analysis of Annexin-V staining. DNA fragmentation was detected when cells were treated with 50 or 100 ppm chlorpyrifos for 4 and 6 h. Chlorpyrifos also induced an increase in intracellular active caspase-3 in Jurkat T cells in a dose- and time-dependent manner, and a caspase-3 inhibitor, Z-DEVD-FMK, significantly inhibited chlorpyrifos-induced apoptosis. These findings indicate that chlorpyrifos can induce apoptosis in human Jurkat T cell cells, and this effect is partially mediated by the activation of intracellular caspase-3.

Chlorpyrifos induces cardiac dysfunction in rabbits

This study was carried out to evaluate the effects of organophosphate (OP) insecticide chlorpyrifos on cardiac morphology and function in rabbits using echocardiography. Twenty New Zealand male rabbits were divided equally into four groups. Rabbits were exposed to chlorpyrifos in drinking water at concentrations of 0, 125, 250 or 375 ppm for 90 days. The comparison among the groups indicated that 375 ppm chlorpyrifos resulted in significant decrease ( p < 0.05) in heart rate (HR), cardiac output (CO), left ventricular fractional shortening (FS), left ventricular ejection fraction (EF), percentage thickening of left ventricle posterior wall (PWT), and significant increase ( p < 0.05) in left atrial diameter (LA), left ventricular internal diameter in end diastole (LVIDD), left ventricular end diastolic (EDV) and end systolic volumes (ESV) compared to those of the control group. These results showed that chlorpyrifos induces cardiac dysfunction in rabbits.

Identifying insecticide-resistant greenbugs (Homoptera: Aphididae) with diagnostic assay tests.

Laboratory bioassays were used to develop a diagnostic assay test for identifying greenburg, Schizaphis graminum (Rondani), populations that are insecticide-resistant. Petri dish assays with chlorpyrifos showed greenbug mortality should be monitored after 2 h of exposure. One-hour exposure did not kill a high percentage of susceptible greenbugs, and a 3-h exposure killed too many resistant greenbugs. Ethanol and methanol were both good solvents for mixing with chlorpyrifos in the petri dish assay. From the laboratory bioassays, four diagnostic concentrations of chlorpyrifos (3, 10, 30, and 100 ppm) were evaluated in the field by Texas A&M University agricultural research and extension entomologists across the Texas High Plains. Results from the diagnostic assay tests were compared with gel-electrophoresis resistance tests to validate resistance detection. The diagnostic assay tests gave the same greenbug resistance identification as the gel-electrophoresis analysis in 21 of 22 field bioassays in 1994 and 35 of 39 field bioassays in 1995. Diagnostic concentrations of 30 and 100 ppm chlorpyrifos killed > or = 85 and > or = 90%, respectively, of greenbugs identified by gel-electrophoresis as susceptible and < 40% and < 55%, respectively, of resistant greenbugs. The diagnostic assay technique is a quick, reliable, and inexpensive method for detecting insecticide resistance in greenbug populations.

Oral to xicity of Various Insecticides, 1990-1991

Abstract Five insecticides (abamectin, chlorpyrifos, dechlorane, permethrin, and sulfluramid) were evaluated as potential bait toxicants for black carpenter ants. All testing was done after sunset, between 2100 and 0100 h, with foragers from colonies nesting in trees. Technical abamectin, dechlorane, and sulfluramid were solubilized in acetone (20 ml) to 25 mg/u,l; 50mg of Tween80 was added to enhance even mixing in the sugar-milk bait. Formulated chlorpyrifos (4 E) and permethrin (2 E) were used, since the above procedure had not been adopted when they were tested. An appropriate volume of concentrate was diluted in given weight of sugar-milk bait (10 g raw sugar in 50 ml whole milk). Fresh sugarmilk dilutions were prepared each evening and transported on ice. Ants were attracted to a feeding station at the terminus of 3-cm diam wooden poles, supported at 50 cm above the ground, originating from a tree where the colony nested. Once ants were traveling along the poles, a bait dish on the feeding station was filled with 1 ml of toxic bait. After ants fed to repletion, and were returning to the nest, they were transferred to plastic boxes (10 per box) with a ventilated lid. This was continued until approximately 30 ants (range: 28 to 31) were dosed. Returned to the laboratory (25 ° 5°C, ambient RH), the ants were provided a moistened dental wick, and observed for cumulative mortality at 6 and 12 h after treatment and then at 12 h intervals for 21 d; dental wicks were wetted daily. At varying DAT, LC^s were estimated by regression of probit mortality vs. log10 of concentration (ppm). LT30S for 500 ppm abamectin, dechlorane, and sulfluramid and 20 ppm chlorpyrifos and permethrin were estimated by regression of cumulative probit mortality vs. logio of time (d); for LTJQS, ants fed untreated bait served as controls monitoring natural mortality.

Effects of endosulfan, chlorpyrifos and their mixtures onBemisia tabaciof Sudan Gezira

Abstract In an attempt to explain the presumed synergism (viz. potentiation) of chlorpyrifos† and endosulfan‡, chlorpyrifos e.c. with endosulfan e.c. at different rates and ratios were tested against Bemisia tabaci (Genn.). Dipped Iubia leaves were used. The additive effect was observed on the LC50 basis, while a potentiation effect was observed at LC50 level. Chlorpyrifos, endosulfan, endosulfan + chlorpyrifos (mix 1, i.e. 10 ppm endosulfan + 14, 10.5, 7 and 3.5 ppm chlorpyrifos), and chlorprifos + endosulfan (mix 2, i.e. 14 ppm chlorpyrifos + 10, 7.5, 5 and 2.5 ppm endosulfan) have shown the following LC50s: 17.37, 9.62, 5.5 and 15.49 ppm, respectively. Following the same order, they showed LC90S of 118.30, 52.67, 13.33 and 23.27 ppm. The slopes of the dosage‐response curves reported were 1.56, 1.76, 3.36 and 7.17, respectively.