Possible aversion learning in the Pacific Coast wireworm

The effects of carbon dioxide and the induction of morbidity on aversion learning in larvae of the Pacific Coast wireworm Limonius canus LeConte (Coleoptera: Elateridae) are discussed. Wireworms preconditioned by exposing them one or four times to odour of Tefluthrin 20SC and Dividend XLRTA [Syngenta Crop Protection (Canada), Inc., Canada] during the induction of temporary morbidity subsequently contact tefluthrin‐treated wheat seeds in soil bioassays for as long as naïve (i.e. not preconditioned) larvae but are repelled four to five‐fold more frequently by Dividend‐treated seeds in soil bioassays than naïve wireworms, suggesting that wireworms are capable of associating a novel odour (i.e. Dividend) with morbidity but require a minimum of 10–15 min subsequent contact time with treated seeds before being repelled. Wireworms preconditioned by exposure to peppermint odour during the induction of morbidity are not subsequently repelled by peppermint odour in soil bioassays, suggesting that wireworms are either not capable of aversion learning or that the presence of a CO₂ source and/or a suitable host plant may override a negative cue (i.e. peppermint odour). In studies conducted in the absence of soil, a host plant and CO₂ production, wireworms are repelled slightly by droplets of 1.0% but not 0.1% peppermint oil. Previous exposure to peppermint odour or contact with peppermint oil‐treated filter paper during one induction of morbidity does not increase the repellency of wireworms to 1.0% peppermint oil significantly. Repellency to 1.0% peppermint oil is almost eliminated when morbidity is induced five times in the absence of peppermint odour but is restored when peppermint odour is present during preconditioning. These findings suggest that wireworm sensitivity to repellent compounds decreases when repeatedly made moribund, although the results are not sufficient to conclude that wireworms are capable of associative learning.     

Repellency of a wireworm, Agriotes obscurus (Coleoptera: Elateridae), on exposure to synthetic insecticides in a soil-less bioassay

A soil-less bioassay arena to test repellency of wireworms (A. obscurus) to insecticides and carrier solvents is described. The bioassay and variables measured distinguish between shorter-range (contact and/or volatile) and longer-range (volatile) repellency. Wireworm positions are recorded every 3 s for 20 min, and average speed, rate of slowing, and longer- and shorter-range repellent behaviors calculated. Shorter-range repellency is determined with a Wireworm Repellency Score (WRS, range 0-100), calculated before contact and after contact with test chemicals. Of two carrier solvents tested, wireworms were strongly repelled by acetone (WRS = 57) but not by water (WRS = 1) when introduced to the bioassay arenas immediately after chemical inoculation. When bioassay arenas were assembled/sealed 2 min after inoculation, acetone elicited no repellency (WRS = 2). When dissolved in acetone in bioassays assembled with a 2-min delay, imidacloprid, chlorpyrifos, lindane, and tefluthrin elicited slight to moderate repellency at the highest concentrations tested (WRS = 30, 48, 42, and 49, respectively). Both longer- and shorter-range repellency increased over the duration of the observation period for lindane and tefluthrin, and shorter-range repellency also increased over the duration of the observation period for chlorpyrifos. Removal of volatiles in the bioassay arena by vacuum considerably affected wireworm movement in the arena, with the repellency elicited by acetone and lindane being significantly reduced. Clothianidin elicited no longer- or shorter-range repellency.     

Environmental and behavioral constraints on the infection of wireworms by Metarhizium anisopliae

Environmental and behavioral factors that affect the infection of wireworms [Agriotes obscurus L. (Coleoptera: Elateridae)] by a unique isolate of Metarhizium anisopliae Sorokin (Hypocreales: Clavicipitaceae) were studied. After wireworms were placed in soil containing 10(6) M. anisopliae conidia/g and incubated at 6, 12, or 18 degrees C, significant disease development and wireworm mortality occurred only in those wireworms incubated at 18 degrees C. At this temperature, mortality was found to be dependant on the time exposed to the contaminated soil, and a minimum exposure time of 48 h was required to cause significant levels of mortality. Despite the restrictive effect of cooler temperatures on disease development and mortality, infected wireworms did not choose temperatures that inhibited disease development when given the opportunity to do so in a separate experiment. Finally, wireworms were repelled by M. anisopliae-contaminated soil at a rate that increased with the soil conidia concentration, but the rate of emigration was reduced when a food source was present. The results of this study indicate that factors including temperature, time exposed to M. anisopliae, conidia soil concentration, and food availability will affect mortality rates of wireworms and are likely to affect field performance of M. anisopliae as a biological control.     

Transitional sublethal and lethal effects of insecticides after dermal exposures to five economic species of wireworms (Coleoptera: Elateridae)

During an insecticide toxicity study involving field-collected dusky wireworm, Agriotes obscurus (L.) (Coleoptera: Elateridae), wireworms exposed dermally to six classes of insecticides exhibited characteristic transitional symptoms of toxicity. These symptoms, collectively termed "morbidity," were categorized as "writhing," "leg and mouthpart movements," or "mouthpart-only body movements." These symptoms could persist for long periods, depending on insecticide and dose, with morbid wireworms ultimately recovering or dying. Additional LC50 and LD50 toxicity studies showed that these stages of morbidity also occurred in four other wireworm species, notably Agriotes sputator (L.), Limonius canus LeConte, Ctenicera pruinina (Horn), and Ctenicera destructor (Brown). In addition, all species exposed dermally to clothianidin moved in significant numbers to the surface of soil in posttreatment holding cups. This movement was not observed when these species were exposed to chlorpyrifos or the control solvent. These findings suggest that toxicity trials involving wireworms should include observations on morbidity, and the duration of trials should continue until symptoms of morbidity cease. The long-term morbidity and potential recovery or death of wireworms exposed to certain insecticides has implications for how laboratory and field studies can be better designed and interpreted in the future.     

Effect of temperature on the morbidity and recovery of the Pacific Coast wireworm, Limonius canus, following contact with tefluthrin-treated wheat seeds

Late instars of the Pacific Coast wireworm, Limonius canus (LeConte) (Coleoptera: Elateridae), were exposed to wheat seeds treated with tefluthrin at 10 g active ingredient/100 kg wheat seed, for 2 min, at 10, 15, 20, and 25 °C. All wireworms were moribund within 20 min of first exposure and recovered fully within 7 h. Morbidity induction time (i) decreased considerably as the temperature (t) was increased from 10 to 15 °C, but did not decrease further when the temperature was increased from 15 to 25 °C. For each temperature, induction time decreased as wireworm weight (w) increased, so that . A strong negative temperature coefficient was observed in wireworm recovery, the time required for recovery (r) after exposure decreasing as both temperature (t) and wireworm weight (w) increased, so that r = 1102.47(w)^?0.1848 * e^?0.1012t. The temperature at which wireworms contact insecticides in the field may significantly affect the induction and duration of morbidity, and determine whether wireworms will become moribund before they are repelled by tefluthrin. The ability of wireworms to recover from tefluthrin‐induced morbidity may seriously limit the efficacy of this insecticide in reducing wireworm populations in the field.     

Mortality of a wireworm, Agriotes obscurus (Coleoptera: Elateridae), after topical application of various insecticides

Ten insecticides representing seven chemical groups were applied at various concentrations topically by using a Potter Spray Tower to evaluate their relative toxicities on the European wireworm Agriotes obscurus L. (Coleoptera: Elateridae). Wireworms were stored at 15 degrees C after exposure to organophosphate (OP) (chlorpyrifos, diazinon), pyrethroid (tefluthrin), thianicotinoid (thiamethoxam, clothianidin), chloronicotinoid (imidacloprid, acetamiprid), phenyl pyrazole (fipronil), organochlorine (lindane), and spinosyn (spinosad) insecticides, and their postapplication health was evaluated weekly for up to 301 d. LC50, LC90, LT50, and LT90 values were calculated for each chemical except acetamiprid, and compared with those of lindane, clothianidin, and chlorpyrifos. Wireworms exposed to OPs died or recovered more quickly (LT50 < 20 d, LT90 < 50 d), than those exposed to all other insecticides tested except tefluthrin (LT50 = 25.5 d, LT90 = 66.5 d). Wireworms exposed to sublethal concentrations of all neonicotinoids quickly became moribund after application but made a full recovery. Wireworms exposed to fipronil at concentrations near the LC90 value showed no intoxication symptoms for up to 35 d, and they did not recover after symptoms developed. For each chemical, increasing the concentration increased the time required for wireworms to recover but decreased the time required to kill wireworms. Fipronil was highly toxic to wireworms (LC50 = 0.0001%), but acetamiprid (LC50 = 1.82%), imidacloprid (LC50 = 0.83%), tefluthrin (LC50 = 0.23%), diazinon (LC50 = 0.54%), and spinosad (LC50 = 0.51%) were not. The toxicity of both clothianidin (LC50 = 0.07%) and thiamethoxam (LC50 = 0.17%) were similar to those oflindane (LC50 = 0.06%) and chlorpyrifos (LC50 = 0.10%).     

Morbidity and recovery of the Pacific Coast wireworm, Limonius canus, following contact with tefluthrin-treated wheat seeds

Late instars of the Pacific Coast wireworm, Limonius canus (LeConte) (Coleoptera: Elateridae), were exposed to wheat seeds treated with tefluthrin at 5, 10, 15, 20, or 30 g active ingredient (a.i.) per 100 kg wheat seed for 1, 2, 4, 8, or 16 min. All wireworms were moribund within 20 min of first exposure and recovered fully within 12 h. The time required for recovery (t_r) after a single exposure increased with duration of exposure (e) and concentration (c), but decreased with wireworm weight (w), expressed as (t_r)^0.5 = 5.2812 + 0.9407e – 0.0259e² + 0.1569c + 0.0254ec – 0.0174w – 0.0057ew. For wireworms exposed to treated seeds for 2 min, the time required for induction of morbidity decreased as concentration of tefluthrin increased and as wireworm weight decreased, expressed as (t_i)^0.5 = 2.613 – 0.039c + 0.018w, where t_i is the induction time of morbidity, and c and w are as above. Wireworms re‐exposed to tefluthrin‐treated seeds after recovery from previous exposure were again moribund within 20 min of exposure, but recovery was significantly more rapid if the second exposure was 2, 4, 6, 8, 12, 18, 24, and 48 h after recovery from first exposure. Recovery from a second exposure was not significantly faster when the second exposure was 96 h after recovery from the first exposure. The ability of wireworms to recover from tefluthrin‐induced morbidity may seriously limit the efficacy of this insecticide in actually reducing wireworm populations in the field.     

Aggregation and mortality of Agriotes obscurus (Coleoptera: Elateridae) at insecticide-treated trap crops of wheat

Agriotes obscurus (L.) wireworms assembled in increasing numbers at rows of treated (Agrox DL Plus seed treatment) and untreated wheat, Triticum aestivum L., planted at increasing densities (0, 0.15, 0.30, and 0.60 seeds/cm). In treated wheat plots at all planting densities, no wireworm damage to seedlings was apparent, and total wireworms taken in core samples in wheat rows increased according to the asymptotic equation y = B0(1 -e(-Blx)), where B0 is the asymptote, B1 is the slope of the initial rise, and x is the seeding density. The number of dead wireworms in treated plots increased linearly and intercepted the asymptotic models (theoretical point at which 100% mortality of assembled population occurs) at 0.95 seeds/cm on 11 June and 1.14 seeds/cm on 18 June 1996. Untreated wheat at all densities planted had severe wireworm damage and significantly reduced stand. Populations that had assembled at the surviving untreated wheat were fewer than in the treated wheat plots, and although increasing with seeding density, did not follow the asymptotic model. The data suggest that A. obscurus populations can be assembled and killed in fallowed fields in large numbers at treated trap crops of wheat over a 19-d period when planted in rows spaced 1 m apart at a linear seeding density of 1.5 seeds/cm.     

Wireworm (Coleoptera: Elateridae) identity, monitoring and damage in sugarcane

Abstract Wireworms (Coleoptera: Elateridae) damage the eyes and young shoots of germinating cane setts in many growing regions. Insecticides can be applied at planting to avoid damage. However, there are no guidelines for deciding on whether treatment is warranted and a sampling method to detect wireworms before planting has not been developed. Baits of rolled oats were tested as a method for detecting wireworms in preplant fallows. In 1995 at Bundaberg, the reduction in crop establishment when treatment was withheld was positively correlated with the catch of wireworms at baits before planting. However, no similar relationship was seen in 1996 or at Mackay in either 1995 or 1996: severe damage was recorded on one farm at Mackay where no wireworms had been found. A sampling plan was developed to estimate wireworm numbers at baits with a fixed level of precision. Wireworms collected at the baits and in samples from established canefields in Queensland and New South Wales included five named and 21 unnamed species from five genera, the most abundant being Agrypnus , Conoderus and Heteroderes . Possible barriers to the adoption of baiting as a decision-support tool are discussed. Development of a reliable monitoring system would require considerably more research, which could not be justified at present.     

Varietal susceptibility of potatoes to wireworm herbivory

1 Wireworms, the soil dwelling larvae of click beetles, Agriotes spp., have recently become a more prevalent pest of potatoes. The present study investigated whether potato varieties showed variable susceptibility to wireworm herbivory, and also tested whether increased susceptibility was associated with lower concentrations of glycoalkaloids. Twelve varieties were originally screened across a range of experimental scales, including laboratory and tunnel experiments and a large‐scale field trial involving over 2000 tubers. 2 In laboratory no‐choice tests, Maris Peer, Marfona and Rooster varieties were significantly more susceptible to wireworm attack, with 63% of tubers showing damage, compared with just 15% of the less susceptible varieties of King Edward, Nadine and Maris Piper. There was also greater tissue consumption and weight gain when wireworms were reared on the most susceptible varieties. 3 In choice tests, wireworms showed a significant preference for those varieties previously identified as being the most susceptible to wireworm herbivory (4.2 holes per tuber) compared with the least susceptible (1.2 holes per tuber). Similar patterns of susceptibility were seen in the field trial, although there was generally more variation in susceptibility. 4 In a tunnel experiment, Marfona and Maris Peer were significantly more susceptibile to wireworm attack (47% of tubers showing damage) compared with Nadine, King Edward and Maris Piper (27% of tubers showing damage). Although Nadine, in particular, had the highest glycoalkaloid concentrations (309.33 mg/kg) and lowest amounts of wireworm herbivory, the relationship between susceptibility and glycoalkaloid concentrations was weak, suggesting that this is unlikely to be the sole mechanism underpinning varietal susceptibility.     

Wireworm populations in relation to crop production: I. A large-scale flotation method for extracting wireworms from soil samples and results from a survey of 600 fields

The wireworm survey in the Eastern Counties revealed many cases where the observed wireworm damage failed to correspond with the estimated field population. A possible explanation for this was the inaccuracy of counts made by picking wireworms out of the soil samples by hand. Tests showed that such methods recovered an extremely variable proportion of the wireworms in the- samples and, on the average, only two-fifths of the larvae were obtained. A modified form of the washing and flotation technique used by Salt & Hollick (1944) was introduced for large-scale work and is described. By this method, ten samples of soil (4 in. diam. and 6 in. deep) bulked together are examined at a time and can be dealt with at the rate of 13 samples per man per hour with an efficiency of 95-100% in the extraction of wireworms. The populations estimated on 600 fields sampled between December 1942 and May 1943 have thrown more light on the size and composition of the wireworm population in grass and arable fields. Inspection of the crop results on fields tested by the washing process showed a much closer relationship between wireworm population and wireworm damage than had been obtained by the hand-sorting method in the previous year.     

DNA barcoding identification and genetic diversity of bamboo shoot wireworms (Coleoptera: Elateridae) in South China

Wireworms are recognized as economically important oligophagous pests of Phyllostachys bamboo shoot, which have caused a huge economic loss in South China. Studies of bamboo shoot wireworm control and management were seriously hampered by the lack of reliable identification of larvae. DNA barcoding has been proved to be an important and useful tool in species identification of morphologically cryptic insects. Accurate knowledge of damage-causing species and the phylogenic structure of elaterids will provide insight into their sustainable and effective management. Here, we use interspecific variation in COI and EF1-a as a robust method of identification and consider the intra- and interspecific genetic variation of bamboo wireworms. This approach has revealed that three Melanotus larvae occurred in Phyllostachys forest. The dominance of one species in different sampling location suggests there maybe underlying difference in habit and host plant preference. These data provide a starting point for determining the distribution of wireworm species feeding on bamboo shoots in South China. The inclusions would further aid identification of wireworm species and relationships between certain wireworm species with specific environments.     

Toxicity of 1,3-dichloropropene and fosthiazate to wireworms (Agriotes spp.)

Wireworms (Agriotes spp.) are sporadic but increasingly important pests of potatoes, sugar beet and cereals. Whilst effective chemical control is possible, the granular organophosphates normally require high rates of application and the seed dressings containing lindane (gamma‐HCH) have been withdrawn from use. The soil fumigant 1,3‐dichloropropene (1,3‐D as Telone II) and the granular nematicide fosthiazate (Nemathorin 10G) are currently used for the control of potato cyst nematodes. We investigated the effects of both of these chemicals on wireworms. Air‐vapour phase toxicities for 1,3‐D against wireworm were LD₅₀ 2.74 mg.litre.day and LD₉₉ 5.05 mg.litre.day. The in vitro soil phase toxicity was LD₉₉ 8.15 mg.litre.day. 1,3‐D soil phase activity against wireworm may be associated more with air‐vapour phase than a soil‐water phase activity. In glasshouse experiments 16.0 mg.litre.day of 1,3‐D gave 75% control. Fosthiazate, which is applied at approximately 2 μg g^?1 of soil for potato cyst nematode control, achieved an LC₅₀ at 3.20 μg g^?1. In both in vitro and glasshouse studies 1,3‐dichloropropene showed high toxicity to wireworm at dosages below the current commercial application rate for potato cyst nematode control and fosthiazate also showed useful efficacy. These chemicals may therefore prove to be valuable additional tools for limiting initial wireworm plant damage or reducing wireworm populations.     

Above- and belowground insect herbivores differentially affect soil nematode communities in species-rich plant communities

Interactions between above‐ and belowground invertebrate herbivores alter plant diversity, however, little is known on how these effects may influence higher trophic level organisms belowground. Here we explore whether above‐ and belowground invertebrate herbivores which alter plant community diversity and biomass, in turn affect soil nematode communities. We test the hypotheses that insect herbivores 1) alter soil nematode diversity, 2) stimulate bacterial‐feeding and 3) reduce plant‐feeding nematode abundances. In a full factorial outdoor mesocosm experiment we introduced grasshoppers (aboveground herbivores), wireworms (belowground herbivores) and a diverse soil nematode community to species‐rich model plant communities. After two years, insect herbivore effects on nematode diversity and on abundance of herbivorous, bacterivorous, fungivorous and omni‐carnivorous nematodes were evaluated in relation to plant community composition. Wireworms did not affect nematode diversity despite enhanced plant diversity, while grasshoppers, which did not affect plant diversity, reduced nematode diversity. Although grasshoppers and wireworms caused contrasting shifts in plant species dominance, they did not affect abundances of decomposer nematodes at any trophic level. Primary consumer nematodes were, however, strongly promoted by wireworms, while community root biomass was not altered by the insect herbivores. Overall, interaction effects of wireworms and grasshoppers on the soil nematodes were not observed, and we found no support for bottom‐up control of the nematodes. However, our results show that above‐ and belowground insect herbivores may facilitate root‐feeding rather than decomposer nematodes and that this facilitation appears to be driven by shifts in plant species composition. Moreover, the addition of nematodes strongly suppressed shoot biomass of several forb species and reduced grasshopper abundance. Thus, our results suggest that nematode feedback effects on plant community composition, due to plant and herbivore parasitism, may strongly depend on the presence of insect herbivores.     

Studies of wireworm population; some effects of cultivation

The number of wireworms in successive collections from five Cambridgeshire fields declined during the first year of cultivation to 25 % of the number present before the fields were ploughed from old grass. The decline in numbers was accompanied by a change in the composition of the wireworm population; the marked inverse correlation between number and size of larvae, which held for the wireworm populations under grass, progressively altered towards uniform numbers of the different size-groups. The incidence of natural control on the different sizes of larvae was obscured by their growth, and more medium-sized and large larvae were lost than would appear from the population-size histograms.
Three groups of factors are considered as contributing to the decline in numbers after ploughing. Direct observation showed that many wireworms were destroyed in the actual process of cultivation. Evidence was insufficient to prove that the physical condition of cultivated soil adversely affects the number of wireworms. Comparison of the smaller size-groups in pasture and in the cultivated fields showed that the wireworm population failed to replenish itself under arable conditions.     

Relative susceptibility of two sweetpotato varieties to storage root damage by sweetpotato flea beetle (Coleoptera: Chrysomelidae) and wireworm (Coleoptera: Elateridae)

The feeding of soil dwelling insects on storage roots is one of the most serious management issues faced by sweetpotato, Ipomoea batatas (L.) Lam. (Convolvulaceae), growers in the southern United States. Field studies were conducted to evaluate the relative susceptibility of two commonly grown sweetpotato varieties to sweetpotato flea beetle, Chaetocnema confinis Crotch (Coleoptera: Chrysomelidae), and wireworms (Coleoptera: Elateridae, various species). The incidence and severity of sweetpotato flea beetle damage was significantly lower in the variety Covington than Beauregard in two small plot replicated studies. Surveys conducted in commercial sweetpotato fields also showed significantly less sweetpotato flea beetle damage in fields planted to Covington compared with those planted to Beauregard. There was no clear evidence of varietal effect on the incidence of wireworm damage in the study. Results indicate that the severity of wireworm damage as measured by the size of feeding scars may be less in Covington than Beauregard.     

Food habits of pasture wireworm,Conoderus exsul (Coleoptera: Elateridae)

Abstract

The food preferences and rates of growth of the omnivorous pasture wireworm, Conoderus exsul (Sharp) were studied. Larvae of soil-living insects were preferred to germinating maize seed, and wireworm growth rate was greater on insect compared with plant food. In glasshouse pot trials, wireworms increased their attack rate as the density of grass grub (Costelytra zealandica (White)) or white-fringed weevil (Graphthognathus leucoloma Boheman) larvae was increased. In field experiments that compared grass grub numbers in cages accessible to wireworms or protected from predators, predation varied with season from a low of 15% in late summer up to 82% in late autumn. White-fringed weevil larval mortality was increased by addition of wireworms in two field experiments, but not affected in a third trial where initial white-fringed weevil density was low. Grass grub mortality was increased by the presence of wireworms in field plots. Adult C. exsul were observed feeding on sweetcorn pollen.     

Assessing the performance of pea and lentil at different seeding densities as trap crops for the management of wireworms in spring wheat

Wireworms, the larvae of click beetles (Elateridae), are difficult to manage due to their habitats and behaviour. Wireworms pose a major threat to the wheat crop in the north‐western USA. Seed treatment with neonicotinoids, biological control management and some cultural controls are recommended to manage these pests. Trap cropping is an emerging way to manage wireworms. In strawberry and potato crops, trap cropping has been found effective at attracting wireworms away from the principal crop. An earlier study in the Golden Triangle area of Montana found that pea and lentil could be effective trap crops for managing wireworms in spring wheat. In the present study, experiments were conducted at two locations. The effectiveness of peas and lentils as trap crops with wheat at different seeding densities was assessed [pea at 0, 4, 8, 16 seeds/sq.ft. or 0, 43, 86, 172 seeds/sq.m.; lentil at 0, 6, 12, 18 OR 0, 65, 130, 194 seeds/sq.m.; both with wheat at 0, 11, 22, or 28 seeds/sq.ft. or 0, 120, 230, 300 seeds/sq.m.] in a randomized design where all three crops were intercropped. Both trap crops were found to be effective in protecting wheat at standard seeding rates of 8 seeds/sq.ft. for pea and 12 seeds/sq.ft. for lentils. At these seeding rates, higher numbers of wireworms were found to be attracted to the trap crop, resulting in higher yield (7%–10%) of the associated spring wheat plant stands at 22 seeds/sq.ft. To develop an effective trap crop strategy, the pea–wheat and lentil–wheat spatial patterns that are possible need to be assessed in further field trials. Proper design and evaluation of the cost–benefit ratio of pea and lentil as trap crops are likely to produce good results for wheat crops in Montana.     

Spinosad interacts synergistically with the insect pathogen Metarhizium anisopliae against the exotic wireworms Agriotes lineatus and Agriotes obscurus (Coleoptera: Elateridae)

We determined that spinosad interacts synergistically with the biocontrol agent Metarhizium anisopliae (Metch) Sorokin to increase the mortality of two wild-collected wireworm species, Agriotes lineatus (L.), and Agriotes obscurus (L.). Bioassays were performed using a M. anisopliae isolate originally acquired from a local wireworm cadaver. M. anisopliae was applied as a soil drench at 3.3 x 10(2) and 10(4) conidia per gram sand, respectively. Soil drenches also were prepared using a commercial formulation of the actinomycete toxins spinosyn-A and spinosyn-D (common name spinosad) at sublethal doses of 1.5, 3, and 6 ppm active ingredient per gram sand. Combined treatments of spinosad and M. anisopliae were synergistic in causing mortality for all spinosad concentrations. Wireworm feeding activity was reduced after exposure to both spinosad and M. anisopliae and was found to be concentration dependent. The high mortality and reduced rate of wireworm feeding suggest that spinosad and M. anisopliae treatment combinations should be tested in the field.     

Influence of preceding crop on wireworm (Coleoptera: Elateridae) abundance in the coastal plain of North Carolina

Three studies were conducted to determine the effect of preceding crop on wireworm (Coleoptera: Elateridae) abundance in the coastal plain of North Carolina. In all three studies, samples of wireworm populations were taken from the soil by using oat, Avena sativa L., baits. Treatments were defined by the previous year's crop and were chosen to reflect common crop rotations in the region. Across all three studies, eight wireworm species were recovered from the baits: Conoderus amplicollis (Gyllenhal), Conoderus bellus (Say), Conoderus falli (Lane), Conoderus lividus (Degeer), Conoderus scissus (Schaeffer), Conoderus vespertinus (F.), Glyphonyx bimarginatus (Schaeffer), and Melanotus communis (Gyllenhal). The effect of corn, Zea mays L.; cotton, Gossypium hirsutum L.; fallow; soybean, Clycine max (L.) Merr.; sweet potato, Ipomoea batatas (L.) Lam.; and tobacco (Nicotiana spp.) was evaluated in a small-plot replicated study. M. communis was the most frequently collected species in the small-plot study and was found in significantly higher numbers following soybean and corn. The mean total number of wireworms per bait (all species) was highest following soybean. A second study conducted in late fall and early spring assessed the abundance of overwintering wireworm populations in commercial fields planted to corn, cotton, peanut (Arachis hypogaea L.), soybean, sweet potato, and tobacco in the most recent previous growing season. C. lividus was the most abundant species, and the mean total number of wireworms was highest following corn and soybean. A survey was conducted in commercial sweet potato in late spring and early summer in fields that had been planted to corn, cotton, cucurbit (Cucurbita pepo L.), peanut, soybean, sweet potato, or tobacco in the most recent previous growing season. C. vespertinus was the most abundant species, and the mean total number of wireworms per bait was highest following corn.