DDE increases the toxicity of parathion to coturnix quail

Adult male Japanese quail (Coturnix coturnix) were exposed to DDE or chlordane in the diet and subsequently dosed with parathion or paraoxon. Pretreatment with 5 or 50 ppm DDE in the diet for 12 weeks resulted in increased cholinesterase (ChE) activity in plasma, but not in the brain. Dietary concentrations of 5 and 50 ppm DDE caused increased susceptibility of quail that were challenged with parathion or paraoxon. The increased mortality resulting from DDE pretreatment was reflected in brain ChE inhibition. The synergistic action of DDE was apparent after 3 days of exposure to 50 ppm DDE and 1 week of exposure to 5 ppm DDE. Birds exposed for 3 weeks to 5 or 50 ppm DDE retained their DDE-potentiated sensitivity to parathion after 2 weeks on clean diet. Chlordane pretreatment resulted in decreased susceptibility (antagonism) to parathion, but not to paraoxon dosage. Implications of differing responses in ChE and mortality among controls, DDE-, and chlordane-pretreated birds after parathion or paraoxon dosage are discussed.     

苹果内吸磷残留量的动态酶化学研究

用Hestrin胆硷酯酶活性测定法,系統研究以不同方式施用内吸磷(E-1059)后,苹果内吸磷残留量的动态变化情况。施药方式有三种:(1) 浸果—仅对树上的苹果进行药浸,树叶和树枝不接触药液。(2) 噴叶—苹果以塑料膜包好后向树上嘖药,只树叶和枝上着药,而苹果不着药。(3) 浸枝——将带有果和叶的一段树枝剪下,断端浸入药液中迫使吸收药液24小时。检测結果:浸果施药后第一天内,苹果可检测出很高的内吸磷残留量(可达2 ppm左右),1天后残留量降到0.75 ppm以下,两周后残留量可降低到接近零;噴叶施药后12天内,經数次检测,均未发现有内吸磷残留;用药液浸枝,虽然第一天树枝吸收了不少的药液,但苹果中几乎检測不出内吸磷的残留,第二天换以水浸枝,却反而检测出内吸磷残留量(将及0.5 ppm),大約10天左右残留量降到接近零。試驗結果说明:一般噴雾时内吸磷的残留主要是由于药液直接接触苹果果皮所致,通过叶和枝内吸輸导至苹果上的药液是微乎其微的;浸果施药后第一天内残留量最高,以后逐漸降低,約两周后降到接近于零;浸枝时迫使吸入药液,但輸导至苹果上的药物甚少,并且内吸輸导需要一定时間,所以第二天残留量最高。关于苹果施用内吸磷的期限,似乎可职适当后延至收获前3或4周。     

Dose-dependent sub-chronic toxicity of diethyl phthalate in female Swiss mice

The experiment was conducted to study the after effects of administering DEP at different doses to female Swiss mice for a period of 90 days. Group I mice were fed on normal diet and water ad libitum. Group II mice were maintained on normal diet mixed with corn oil at 8.25 mg/kg of the diet/day as oil control. Group III, IV and V mice were given diethyl phthalate dissolved in corn oil mixed with the diet at 10, 25 and 50 mg/kg of the diet/day, which is approximately equal to 1.25, 3.125 and 6.25 mg/kg body weight/day. A significant dose dependent increase was observed in serum acid phosphatase (ACP) whereas, serum and liver triglycerides levels showed a significant increase only in the high-dose treated group. Significant dose-dependent increase in serum aspartate and alanine aminotransferase (AST and ALT) and liver glycogen was observed. Serum lactate dehydrogenase (LDH) was significantly increased only in 25 and 50 ppm DEP-treated mice. Liver cholesterol was significantly increased in all the treated groups. Liver histology by light microscopy showed intracellular vacuolations in all the treated groups which was much more evident in the 25 and 50 ppm DEP-treated mice while hepatocellular degeneration and hypertrophy of the hepatocytes was evident in 50 ppm DEP-treated mice. Proliferation of mitochondria and peroxisomes was evident in the electron micrographs of the 10 ppm DEP-treated mice while 25 and 50 ppm DEP-treated mice showed increase in lipid droplets and severe mitochondrial proliferation.     

Prochloraz,a potent inducer of the microsomal cytochrome P-450 system

Prochloraz (N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]-imidazole-1-carboxamide), a recently developed agricultural fungicide, is a potent inducer of microsomal enzymes. Rats fed 7 days with a prochloraz-contaminated diet (2500 ppm) showed an increase in hepatic cytochrome P-450, cytochrome b₅, and microsomal protein level; aniline hydroxylase, 7-ethoxycoumarin dealkylase, 7-ethoxyresorufin dealkylase, NADPH-cytochrome c reductase, and epoxide hydrolase were significantly induced. At a lower dose (100 ppm), only an increase in cytochrome P-450 and 7-ethoxyresorufin dealkylase was noticed. As shown with aniline hydroxylase and 7-ethoxycoumarin dealkylase, prochloraz is also a potent inhibitor of drug-metabolizing enzymes. The interaction of prochloraz with hepatic microsomal fraction from rat liver was also studied. Prochloraz binds to oxidized cytochrome P-450 to produce a type II spectral change; the compound also binds to reduced cytochrome P-450. The binding of some ligands (7-ethoxycoumarin, n-octylamine, aniline, and imidazole) to oxidized cytochrome P-450 was determined after induction by prochloraz. Japanese quails (Coturnix coturnix) fed 7 days with a prochloraz-contaminated diet (2000 ppm) showed a dramatic increase in liver weight (2.5-fold) and both hepatic and duodenal cytochrome P-450 (9- and 12-fold, respectively).     

Systemic effects of a neem insecticide onLiriomyza huidobrensis larvae

In an effort to expand the spectrum of larvicides effective against the pea leafminer,Liriomyza huidobrensis (Blanchard), we studied the effects of a neem-based insecticide (Neemix-45) on the development of the leafminer under laboratory conditions. Bean plants were treated with a soil drench of 1, 5, 10 or 25 ppm azadirachtin or by dipping leaves in 1 or 15 ppm azadirachtin at various times before or during the development of the leafminer. Treating the plants with the neem insecticide before exposure to egg-laying adults had a greater effect on inhibiting the development of pupae and adult eclosion than treatment at the 1st-instar larval stage. The systemic effects from a soil drench had a greater adverse effect on pupation and adult eclosion than leaf dipping. Drenching plants with 1 ppm azadirachtin 24 h before exposure to adults had a greater effect (0% adult eclosion) than leaf dipping at the same time period and concentration (15. 6% adult eclosion). Similar results were obtained when drenching plants infested with lst-instar larvae with 1 ppm azadirachtin (11. 7% eclosion)vs dipping leaves at the same time period and concentration (44. 7% eclosion).     

Protein metabolism in Spodoptera litura (F.) is influenced by the botanical insecticide azadirachtin

Azadirachtin, as a botanical insecticide, affects a wide variety of biological processes, including reduction of feeding, suspension of molting, death of larvae and pupae, and sterility of emerged adults in a dose-dependent manner. However, the mode of action of this toxin remains obscure. By using proteomic techniques, we analyzed changes in protein metabolism of Spodoptera litura (F.) induced by azadirachtin. Following feeding 4th instar larvae of Spodoptera litura (F.) with an artificial diet containing 1 ppm azadirachtin until pupation, 48 h old pupae were collected and protein samples prepared. Total soluble protein content was measured and the results showed that azadirachtin significantly influenced protein level. Moreover, the proteins were separated by 2-DE (two-dimensional polyacrylamide gel electrophoresis) and 10 proteins were significantly affected by azadirachtin treatment when compared to an untreated control. Six of these proteins were identified with peptide mass fingerprinting using MALDI-TOF-MS after in-gel trypsin digestion. These proteins are involved in various cellular functions. One identified protein may function as an ecdysone receptor, which regulates insect development, and reproduction. It is suggested that the botanical insecticide azadirachtin affects protein expression and the azadirachtin-related proteins would be essential for a better understanding of the mechanisms by which neem toxins exert their effects on insects.     

Inhibition of the fucosterol-24(28)-epoxide cleavage enzyme of sitosterol dealkylation in Spodoptera littoralis larvae

The conversion of sitosterol into cholesterol and the effect of inhibitors on the dealkylation reaction has been studied in Spodoptera littoralis Boisd. Using a microsomal preparation from the midgut of the larvae [³H]fucosterol and [³H]fucosterol-24,28-epoxide were converted into desmosterol and cholesterol in vitro, and a series of inhibitors were tested using the latter substrate. Triadimefon [1-(4-chlorophenox)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one] strongly inhibited the cleavage enzyme at 2 μM. In a functional group study we observed that (i) the phenoxy substituent was more strongly inhibitory than the corresponding benzyl, and (ii) when the ketone is reduced to the secondary alcohol in either phenoxy or benzyl series, inhibition decreased markedly. In the benzyl series of compounds we found that (iii) a 2,4- or 2,6-dichlorophenyl gave greater inhibition than mono-, tri-, or pentachlorophenyl derivatives, and (iv) changing the heterocyclic ring gave activity in the order 2-pyridyl=3-pyridyl=imidazole>pyrazole>triazole. In the triazole series, substitution of the hetero ring did not abolish inhibition. When either triadimefon or 22,25-diazacholesterol was incorporated into a diet (1000 ppm) containing sitosterol plus campesterol as the only sterol supplements and fed to final larval instar insects, the weight of the insects throughout the instar was reduced and the duration of the instar increased. Insects reared from the early third-instar stage on such a diet containing amounts of triadimefon had reduced percentages of cholesterol and desmosterol in the final larval instar with a proportional increase in the sitosterol level. Thus, inhibition of side chain cleavage has been obtained in vitro and in vivo, but the high concentrations of inhibitor required preclude the enzyme as a target for a novel class of insecticide.     

Dietary effects upon biological performance and lambda-cyhalothrin susceptibility in the multicolored Asian lady beetle, Harmonia axyridis

Considered a generalist species among the coccinellids, the multicolored Asian lady beetle Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae) feeds upon small arthropods and non-prey plant products, a practice which might enhance its ability to colonize various ecosystems but carries the potential to expose it to prey quality variation and insecticide use. Thus, we examined the effect of four different diets on the development, reproduction, and response to the insecticide lambda-cyhalothrin in this species. Three groups of larvae received laboratory-reared diets: (i) eggs of Anagasta kuehniella (Zeller) (Ak); (ii) eggs of Sitotroga cerealella (Olivier) (Sc); and (iii) eggs of A. kuehniella + S. cerealella at the proportion 1:1; and one group received wild-caught cotton aphids, Aphis gossypii Glover (Ag). Notwithstanding the generalist feeding behavior of H. axyridis, development and reproduction results were superior with diets of Ag or Ak compared with the diet combining 1:1 Ak + Sc or the diet of Sc eggs only. Furthermore, the Sc diet did not result in satisfactory development and reproduction. Despite this significant variation in biological responses, insecticide susceptibility studies using adults that had been reared on these diets showed no statistically significant differences in susceptibility to the lambda-cyhalothrin.     

Fate of endosulfan in rats and toxicological considerations of apolar metabolites

[¹⁴C]Endosulfan, α or β isomers separately, was administered to rats as a single oral dose and as a dietary supplement for 14 days. No appreciable differences were observed in the fate of the two isomers. Five days after the single dose, 75% of the dose had been voided in the feces and 13% in the urine. Of the total radiocarbon consumed in the diet after 14 days, 56% had been eliminated in the feces and 8% in the urine. Bile collection studies showed that up to 47% of a single oral dose was eliminated from the liver via this route; enterohepatic circulation was not apparent. Maximum [¹⁴C]endosulfan equivalents in body tissue occurred in the kidney and liver, 3 and 1 ppm, respectively, after 14 days of feeding 5 ppm of endosulfan. Apolar metabolites in the excreta and/or tissues were a minor portion of the total residues and consisted of the sulfate, diol, α-hydroxy ether, lactone, and ether derivatives of endosulfan. The sulfate was slightly more toxic to mice than endosulfan, while the other products were less toxic. Neither endosulfan nor its metabolites were active in the Salmonella mutagenicity test. Endosulfan in the diet of rats for 28 days at 50 ppm did not induce liver oxidase enzymes, alter liver or kidney weights, or influence the rate of weight gain of the animals.     

Residues of tetrachlorvinphos and its breakdown products on treated crops. III.—Residues on a range of field crops

A wide range of crops including top fruit, cereals, brassicas, root vegetables and cotton from field trials in several countries in 1965, 1966, 1967 and 1968 have been analysed for residues of tetrachlorvinphos (Gardona, trans-homer of dimethyl 1-(2′,4′,5′-trichlorophenyl)-2-chlorovinyl phosphate) foliar insecticide, its isomer and its potential breakdown products. The residues under field conditions were mainly of tetrachlorvinphos, its isomer and 1-(2′,4′,5′-trichlorophenyl)ethan-1-ol in free and sugar-conjugated forms. Tetrachlorvinphos was not unduly persistent on the crops and its initial half-life varied from 2 days on cabbage, to 7 days on potato foliage and to 12 days on pears (after the last of five applications). From one week after the final application onwards the highest residues of tetrachlorvinphos observed were on olives (1 ppm after 18 days after a single application of 0·1 % active material), maize leaf (2·8 ppm at 9·5 weeks after the last of two applications at 3 kg/ha), and cabbage (1·9 ppm at 12 days after the last of three applications at 0·5 kg/ha). The maximum residues of the alcohol in the free form were 3·2 ppm on maize leaf at 8 weeks from the second application at 1·5 kg/ha and in the conjugated form were 1·0 ppm on cauliflowers at 6 days after the last of four applications at 0·5 kg/ha.     

Synergism of organophosphorus insecticides by diethyl maleate and related compounds in house flies

The toxicity of several organophosphorus and one carbamate insecticide for house flies is enhanced by simultaneous administration of diethyl maleate. Synergism factors vary from 2 to 116 and are strongly dependent on the combination of strain and insecticide studied. In general, it seems that thiono compounds are less synergized than their oxon analogs. Comparison of some analogs of maleic acid esters showed that the diethyl ester was not the most active compound. trans-Phenylbutenone was found to be a good alternative for diethyl maleate. Both diethyl maleate and trans-phenylbutenone deplete glutathione in the flies, but this depletion per se is certainly not the most important mode of action. In vitro experiments made clear that sufficient glutathione remained to permit a substantial insecticide degradation rate. Moreover, treatment of the flies with diethyl maleate 2–4 hr before the insecticide application resulted in a partial or complete disappearance of synergism in a period in which the glutathione concentration in the flies was still very low. Apart from this effect on the glutathione levels in the insect tissues it appeared from further experimental work in vitro that both compounds had a direct inhibitory effect on glutathione-dependent transferase(s) as well as on oxidative enzymes involved in insecticide degradation. The contribution of these reactions to the eventual synergism factor is discussed.     

Antifeedant activity of fruit and seed extracts ofMelia azedarach andazadirachta indica on larvae ofSesamia nonagrioides

Methanolic extracts of seeds and fruits of the chinaberry tree,Melia azedarach L. (Meliaceae), showed strong antifeedant activity against 2nd instar larvae ofSesamia nonagrioides Lefèbvre (Lepidoptera: Noctuidae), a very serious pest of maize(Zea mays L.) in Mediterranean countries. Extracts were applied in an artificial diet at concentrations of 1000 and 2000 ppm. The parameters used to evaluate the activity were larval growth rates; quantity of food ingested; phagodepression/phagostimulation index; quantity of frass produced; quantity of material ingested; duration of larval development; and cumulative mortality. Seed extract showed high bioactivity at both doses, while fruit extract proved to be less active, and only at the higher dose used (2000 ppm) did it display a slight antifeedant activity. The activity of theM. azedarach seed extract at the higher dose (2000 ppm) was comparable to that of pure azadirachtin applied at a dose of 1.25 ppm, or to ‘Mubel’, a commercial extract ofAzadirachta indica A. Juss. (Meliaceae), applied at a dose of 75 ppm.     

Sublethal effects of azadirachtin on lipid metabolism and sex pheromone biosynthesis of the Asian corn borer Ostrinia furnacalis

Azadirachtin has remarkable toxic and growth inhibitory effects on Ostrinia furnacalis (Guenée) (Lepidoptera: Pyralidae). In this study, sublethal effects of azadirachtin on fatty acid metabolism and sex pheromone biosynthesis in O. furnacalis were investigated. Quantities of fatty acids were significantly reduced when larvae were fed a diet containing azadirachtin at 0.1?C10?ppm. After 10?days, fatty acids were reduced by 50% on a diet treated with 10?ppm azadirachtin; the relative composition of fatty acids was also affected. The relative proportion of C18:2 fatty acid decreased significantly in adult survivors, correlating with decreased fecundity. Furthermore, sex pheromone titers in adults were inversely proportional to dietary azadirachtin concentration, and reduced by 50% relative to controls when larvae were fed a diet containing 10?ppm azadirachtin. However, there were no effects of azadirachtin on pheromone blend ratios. Our results suggest that reductions in fecundity and pheromone titer in O. furnacalis are associated with alterations in lipid metabolism by azadirachtin, although these effects are not linked to a reduction in consumption.     

Induction of prolonged larval feeding stage by juvenile hormone analogues inTribolium Castaneum

Dietary ZR-512 and ZR-619 at concentrations of 10 — 1000 ppm induced prolongation of the larval feeding period up to tenfold, increasing larval weight up to double that of untreated larvae. A comparison study of four juvenoids, using 200 ppm of ZR-512, ZR-515, ZR-619 or ZR-777, showed that ZR-515 elicits the highest larval weight (6.2 mg) and ZR-777 the lowest (3.6 mg). In all cases a pronounced enhancement of larval weight — of 50 — 250% relative to untreated larvae (2.4 mg) — was obtained.Tr. castaneum larvae reared up to their 3rd instars on a diet containing 100 ppm of ZR-512, ZR-515, ZR-619 or ZR-777 and then transferred to a juvenile hormone-free diet, were not affected. The period between 4th instar larva and pupation should therefore be considered as critical for juvenile hormone effect. The induced prolongation of the larval stage after juvenile hormone treatment was followed by a pronounced enhancement of cuticle phenoloxidase activity, indicating an alteration of the larval biochemical processes. Although juvenile hormone treatment inhibitsTr. castaneum pupation and emergence, it markedly prolongs larval feeding stage and weight and thus accelerates damage.     

Residues of tetrachlorvinphos and its breakdown products on treated crops. II.—Residues on apples

Apples treated with tetrachlorvinphos (Gardona, trans-isomer of dimethyl 1-(2′,4′,5′-trichloropheny1)-2-chlorovinyl phosphate) insecticide under field conditions in several countries in 1965, 1966 and 1967 have been analysed at intervals after treatment for residues of tetrachlorvinphos itself, its cis-isomer and seven potential breakdown products. Residues of up to 10 ppm of tetrachlorvinphos were detected immediately after the last of three applications of tetrachlorvinphos (diluted to 0.16% active material). The initial half-life of the tetrachlorvinphos was on average about 0.5 weeks under U.K. conditions and only 10% of the tetrachlorvinphos remained unchanged at 2 weeks after application. The overall chemical persistence of the wettable powder formulation was not significantly different from that of the emulsifiable concentrate formulation. Within 8 weeks of the application the residues were mainly of tetrachlorvinphos itself, its cis-isomer and the alcohol 1-(2′,4′-5′-trichlorophenyl)ethan-l-ol, in free and sugar-conjugated forms. The residues of the conjugates of this alcohol (up to 0.92 ppm) were generally present in higher concentration at 6-8 weeks after the application than were the residues of the other components. Whilst residues of other breakdown products were detected on the apples their individual residues were below 0.05 ppm and generally below 0.01 ppm at 6 weeks or more after the last of several applications of tetrachlorvinphos.     

Toxicity and dissipation of soil insecticides applied in the management of arecanut white grub, <Emphasis Type="Italic">Leucopholis burmeisteri</Emphasis> Brenk. (Coleoptera: Scarabaeidae)

White grubs, Leucopholis spp. are subterranean pests of arecanut grown in South India. Grub infestation leads to yellowing, stem tapering, and crown size and yield reduction. Use of chemical insecticide to mage the white grubs gives varying degree of success. Hence an attempt was made to screen newer and safer insecticides. Imidacloprid (LC₅₀ at 120 h = 16.849 ppm on III instar larvae), chlorpyriphos (LC₅₀ = 14.242) and bifenthrin (LC₅₀ = 12.797 ppm) were identified as effective insecticides. Evaluation of these insecticide in the field over two year period indicated the following efficacy in reducing larval population: chlorpyriphos @ 4 kg a.i/ha (83.31%) > bifenthrin @ 4 kg a.i./ha (82.83%) > imidacloprid @ 0.24 kg a.i./ha (75.84%) > bifenthrin @ 2 kg a.i./ ha (74.26%) > chlorpyriphos @ 2 kg a.i./ha (69.15%) > chlorpyriphos @ 1 kg a.i./ha (61.79%) > imidacloprid @ 0.12 kg a.i./ha (56.54%) > bifenthrin @ 1 kg a.i./ha (54.34%) > imidacloprid @ 0.06 kg a.i./ha (41.47%). Bifenthrin in soil persisted for a longer period than chlorpyriphos. On the day of application, 59.46 ppm bifenthrin residue was recovered from soil. On 10th day, it was 7.29 ppm which decreased to 2.59 ppm on 30th day and was beyond detection limit on 65th day. Chlorpyriphos exhibited a rapid degradation in the initial stage; 27.46 ppm residue on the day of application, which further reduced to 0.964 ppm on 10th day, and was below the detection limit on the 30th day. Growth of Trichoderma harzianum was not affected by bifenthrin even up to 40 ppm concentration. However, chlorpyriphos affected the growth of Trichoderma at higher than 5 ppm dose. Similarly, imidacloprid inhibited the colony growth from 2 ppm onwards. Having high lipophylic property and contact toxicity, bifenthrin would be an ideal alternative insecticide to chlorpyriphos for the management of white grubs in palm garden, which is safe and long persisting.     

Pesticide residues in the total diet in Canada

A total diet, representative of a Canadian's daily food intake was formulated, grouped by types of food, and prepared as for eating. Analysis of these composites for residues showed eleven organochlorine but no organophosphorus pesticides. Residues were low and would yield an average total daily intake of 24μg/person/day. The level of arsenic was determined on one-quarter of the samples and was found to be consistently below 0.1 ppm.     

Effects of sublethal concentrations of fenitrothion on beet armyworm (Lepidoptera: Noctuidae) development and reproduction

We present data on the effects of various concentrations of the organophosphorus insecticide, fenitrothion, on development, reproduction and eggshell structure of Spodoptera exigua. The insecticide did not change the male/female ratio in tested populations. The pesticide-exposed larvae were significantly smaller than the controls and their pupation was delayed. These changes were not proportionally concentration-dependent. After imaginal molting experimental females laid significantly fewer eggs than controls. This effect was the same whether one or both members of a mating pair were exposed to fenitrothion during the larval stage. In the egg stage the insecticide caused serious malformations of the eggshell. The exposure caused other types of clearly abnormal development of eggs: two micropylar regions were noticed. Hence, even a low concentration of fenitrothion in the diet can lead to serious disturbances in reproduction and thus possibly at the population level.     

Penetration of insecticides through the foregut of the honeybee (Apis mellifera L.)

The rates of penetration of ¹⁴C-labeled insecticides (parathion, carbaryl, and dieldrin) through the foregut of the honeybee (Apis mellifera L.) were measured in vitro and in vivo. Uptake of the insecticides from the lumen of the foregut into foregut tissue was directly proportional to insecticide lipophilicity, but penetration through the foregut was not. Of the three insecticides studied, parathion appeared to possess the optimal physicochemical characteristics required for penetration. The uptake of carbaryl and release of dieldrin by the foregut tissues may limit their respective penetration rates. Insecticide penetration was found to be inversely proportional to the sucrose concentration in the lumen of the foregut in both in vitro and in vivo studies. The oral toxicity of carbaryl showed a similar dependence on the sucrose concentration of the solution in which the insecticide was fed. The data presented indicate that the honeybee foregut is permeable to lipophilic compounds and strongly suggest that this permeability may contribute substantially to the toxicity of orally ingested insecticides in this insect.     

Host plant stimulation of detoxifying enzymes in a phytophagous insect

The midgut microsomal aldrin epoxidase of variegated cutworm larvae (Peridroma saucia, Hübner) fed bean or peppermint leaves was up to 10 and 45 times more active, respectively, than that of larvae fed a basic control diet. Large increases in oxidase activity and cytochrome P-450 levels also occurred in larvae fed mint plant constituents such as menthol menthone, α-pinene, and β-pinene. Mint-fed larvae were more tolerant of the insecticide, carbaryl, than bean-fed larvae.