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%).     

Soil bioassay for studying behavioral responses of wireworms (Coleoptera: Elateridae) to insecticide-treated wheat seed

A bioassay for observing wireworm behavior in soil is described. The bioassay permits analysis of orientation, feeding, repellency, and postcontact toxicity behaviors of wireworms in response to insecticide-treated wheat seeds. Wireworm positions were recorded every 5 min for 3 h, and the time required to orient to and contact seeds, and the duration of individual feeding events, was calculated. Both avoidance (before contact with seeds) and repellency (after contact) were quantified. A high proportion of Agriotes obscurus (0.95), Limonius canus (1.00), Ctenicera pruinina (0.80), Melanotus communis/dietrichi (0.80), and Hypolithus sp. (0.70) larvae contacted untreated wheat seeds and began feeding within 120 min when seeds were preincubated for 60 min in soil with 20% moisture. A smaller proportion of A. obscurus contacted seeds if seeds were not incubated in the bioassay before wireworm introduction (0.80) or in soil with 10% moisture (0.65). L. canus larvae required a significantly shorter time (25.3 min) to contact seeds if seeds were incubated for 60 min than if seeds were not incubated before wireworm introduction (43.1 min). Wireworms exposed to untreated seeds and seeds treated with the fungicide Dividend XLRTA fed normally (i.e., sustained feeding for at least 60 min), but a significant proportion of wireworms exposed to seeds treated with Tefluthrin 20 CS (containing the synthetic pyrethroid tefluthrin) fed for 15 min or less and were subsequently repelled. Wireworms exposed to Vitavax Dual (containing the organochlorine lindane) were not repelled after feeding and showed symptoms of illness for up to 28 d before making a full recovery (89%) or dying (11%).     

The biology and management of wireworms (Agriotes spp.) on potato with particular reference to the U.K.

1 This paper reviews and interprets relevant work on the biology and management of wireworms (Agriotes spp.) within the context of potato production in Europe, with particular reference to the U.K. Although the review concentrates on Agriotes spp., the extensive world literature on other Elateridae of economic importance is also drawn upon. 2 Possible reasons for the apparent increase in the importance of wireworms on the potato crop are discussed, followed by a review of wireworm biology, risk assessment techniques (soil sampling, bait trapping and adult pheromone trapping), crop damage, and cultural, biological and chemical control methods. 3 It is clear that the process of site risk assessment followed by appropriate control measures (usually insecticide use) will remain the mainstay of wireworm management programmes. However, there is considerable scope for adopting new risk assessment techniques, such as pheromone trapping of adult beetles. 4 These control measures will need to be underpinned by a greater understanding of wireworm biology, particularly adult dispersal. Factors affecting the initiation and maintenance of wireworm populations in individual fields also require further study. The current use of insecticides could also be optimized by a better appreciation of the interactions between insecticide use, potato variety choice and harvest dates.     

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.     

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.     

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.     

Predation of Thereva nobilitata (Fabricius) (Diptera: Therevidae) on Agriotes obscurus L. (Coleoptera: Elateridae)

Little is known about the natural enemies of wireworms (Coleoptera: Elateridae), but there are frequent anecdotal reports of (usually unnamed) stiletto fly larvae (Diptera: Therevidae) preying on various species. We observed larvae of Thereva nobilitata (Fabricius) feeding on larvae of the dusky wireworm, Agriotes obscurus L., during the summer of 2011, in Agassiz, British Columbia. This finding is of interest as: both the predator and the wireworm are introduced species to this area from Europe; T. nobilitata is uncommon in North America; and this predator has not been associated with any wireworm species previously. We observed that larvae of male and female T. nobilitata will feed on various sizes of A. obscurus larvae, most feeding being carried out by the smallest T. nobilitata larvae. These findings suggest future work should assess the potential for therevid larvae as top‐down regulators of Agriotes larvae under field conditions.     

Food Preference of Wireworms Analyzed with Multinomial Logit Models

Many species of wireworms (larvae of click beetles, Elateridae) are poly- phagous root herbivores. In grasslands under restoration succession with various grass species, we aim to determine the role of wireworms in aboveground vegetation succession. Therefore, it is crucial to know whether wireworms prefer some food plants to others. We have investigated the root preference to different grass species for Agriotes obscurus and Athous haemorrhoidalis and whether these preferences can be explained by covariates. In Experiment 1, individual wireworms could choose between four different plants, one of each species (Anthoxanthum odoratum, Festuca rubra, Holcus lanatus, and Lolium perenne). In Experiment 2, groups of wireworms were released into the soil in the center of 16 plants (4 from each species). We used multinomial logit models (MLMs) to analze the data. In the appendix the use of multinomial response models is clarified with a fictitious example, using the SAS statistic software package. No preference was found in Experiment 1. In Experiment 2 we found differences in attractiveness of plant species depending on wireworm species: A. obscurus preferred grass species from nutrient-rich grasslands (L. perenne and H. lanatus). Both wireworm species disliked F. rubra. The distance from the release point influenced the probability of being found at a certain place at the end of the experiment: wireworms tended to stay in the proximity of the release point. A. haemorrhoidalis was more often found farther from the point of release than A. obscurus. Dispersal was farther from the release point in experiments with young plants (6 weeks) compared to older ones (9 weeks). Results are discussed in a broad ecological context.     

Preventive application of an entomopathogenic fungus in cover crops for wireworm control

Efficacy of the Metarhizium brunneum Petch (Hypocreales: Clavicipitaceae) strain ART2825 for control of wireworms (Agriotes obscurus (L.), Coleoptera: Elateridae) was examined in a semi-field pot experiment. Pots were treated in late summer during sowing of spring oat as a cover crop. Survival of wireworms was assessed four weeks after their release in October 2013, and 30 weeks after release in April 2014. Viability and persistence of the fungus was determined by counting colony forming units from substrate samples and microsatellite analyses of recovered Metarhizium isolates. The number of colonies detected in the substrate in October 2013 increased with increasing concentrations of applied conidia, and no significant reduction was observed at the second evaluation date in April 2014. Increasing conidia application rates significantly increased mycosis and reduced wireworm survival, to a level comparable to that of treatment using insecticide-coated oat seeds. The preventive application of M. brunneum conidia to reduce wireworm populations in cover crops, preceding a damage-sensitive crop like potatoes, may be a promising biocontrol strategy.     

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.     

WIREWORM POPULATIONS IN RELATION TO CROP PRODUCTION: II. POPULATION CHANGES IN GRASSLAND

Six grass fields were sampled once a fortnight from July 1943 to September 1944, and the wireworms in the samples counted by the washing and flotation method.
The counts from twenty standard samples showed huge fluctuations which rendered them practically valueless as estimates of wireworm populations when treated singly. When treated as running means of four consecutive samplings, the counts showed certain seasonal trends, with minimum populations in July and August, rising populations throughout the autumn, maximum populations in the months from January to April and a sharp decline to the minimum populations again from April to July. On the average, the counts taken in winter were twice as high as those taken in the summer months.
The fluctuation was evident in all size groups based on larval length but was most marked in the wireworms 'under 4 mm.', '4 mm.' and '5 mm.'
Samples taken to depths of 12 and 24 in. showed that on the average about 75 % of the wireworms were found in the 0–6 in. layer and about 90% in the 0–12 in. layer. These proportions varied considerably with the seasons.
The seasonal changes in wireworm populations observed do not correspond with those expected from the life history of Agriotes spp. Possible explanations for this anomaly are discussed, but it cannot be attributed to any known technical or biological factor. Several possibilities remain to be explored.     

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.     

Antipredator Behavioral Traits of some <Emphasis Type="Italic">Agriotes</Emphasis> Wireworms (Coleoptera: Elateridae) and their Potential Implications for Species Identification

Many insects show a typical antipredator behavior. The two simplest tactics are immobilization and flight. The antipredator behavior of wireworms, the soil-dwelling polyphagous larvae of click beetles, has not yet been investigated. Birds are known to attack wireworms. Our experimental method (picking up and dropping wireworms) mimics the first attack of a predator, such as a bird. In Europe, some Agriotes species are of particular importance as crop pests. As these species differ considerably, in ecology, damage threshold, and pathogen resistance, knowing more about the species specific biology and behavior will support the establishment of successful control measures. In an extensive microcosm study, we observed the antipredator behavior of wireworms belonging to four different Agriotes species (A. lineatus, A. obscurus, A. sordidus, and A. ustulatus) before and during digging into the soil after a startle-stimulus. We recorded wireworm immobility frequency and duration, and locomotor activity at three temperatures. We also analyzed genetic and morphologic attributes of A. lineatus larvae from two different origins. Following behavior types were found reflecting different escape tactics: (a) distinct tonic immobility (A. lineatus), (b) brief/inconsistent tonic immobility (A. obscurus, A. sordidus), and (c) immediate fleeing/burying (A. ustulatus). Additionally, we found small but significant differences in morphology, behavior, and genetics (PCR results) between A. lineatus larvae originating from the Netherlands and those originating from Germany. The biological information we gathered about each species will further increase the understanding of these insects and improve interpretation of future experimental data. In addition, the described behavioral differences between Agriotes obscurus and A. lineatus wireworms may represent a useful additional criterion in morphological species identification.     

Differential responses of three Agriotes click beetle species to pheromone traps

1 Previous work had suggested that adult male click beetles (Agriotes spp.) show differential responses to species specific pheromone traps. This hypothesis was tested using mark–release–recapture methods to estimate the maximum sampling range and the effective sampling area of traps for three species. 2 Captured beetles of the species Agriotes lineatus, Agriotes obscurus and Agriotes sputator were marked to show the direction of release, the distance of the release point from the trap and the replicate. Analysis of variance showed that there were significant differences in recapture rates between species and release distances. There were no significant differences between release direction and replicates. 3 Calculated linear speeds suggested differences in movement rates in the order: A. lineatus > A. obscurus > A. sputator. There were also substantial differences between the species in the maximum sampling ranges and effective sampling areas of the traps. These placed the species in the same order. 4 The results are used to estimate the minimum cost of mass trapping programmes to prevent males from mating, giving values of €165/ha/year (A. lineatus), €247.5/ha/year (A. obscurus) and €2343/ha/year (A. sputator). 5 Implications for the use of pheromone traps in wireworm pest management are discussed. It is concluded that current U.K. recommendations based on the cumulative total catch of the three species over a sampling season can be improved by considering the spatial relationships between the adult trapping system and larval distribution. The current constraint to this is the general inability to separate wireworms into species.     

Microbial population of the digestive tract of click beetle larvae (Elateridae,Coleoptera)

The composition and functional structure of the intestinal microflora of three wireworm species (Agriotes obscurus (L.), Selatosomus aeneus (L.), and Ampedus pomorum (Herbst)) with different dietary regimes were studied. The total abundance of the microorganisms was evaluated by fluorescent microscopy, the group composition was assessed by inoculation on a solid glucose-peptone-yeast medium, and the functional diversity was estimated by multisubstrate testing. It was noted that, in the intestine of the larvae, the total number of microorganisms was lower by 1–2 orders of magnitude than in the soil and decaying wood. It was found that the composition of the intestinal microbial communities of wireworms was radically different from that of the substrate: the Bray-Curtis coefficient did not exceed 0.25. It was found that native forms accounted for more than half of the total number of saprotrophic bacteria: in the larvae, Gram-positive cocci, enterobacteria, Vibrionaceae, Acinetobacter, and some genera of coryneform bacteria, which were absent in the soil and wood, prevailed. The micromycetes were either absent (Agriotes) or were found in insignificant quantities (Selatosomus, Ampedus). In Selatosomus, apart from the intestinal forms, representatives of Mezorhizobium, Nocardioides, and Erwinia, occurring on plant substrates, were observed.     

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.     

Evaluation of trap crops for the management of wireworms in spring wheat in Montana

The polyphagous larvae of click beetles (Coleoptera: Elateridae) are major pests of spring wheat in Montana, USA. Presently available insecticides are unable to provide control over wireworm populations, and the use of natural enemies has not been successful under field conditions. In this study, we examined the effect of seven trap crops: pea, lentil, canola, corn, durum, barley, and wheat, for their attractiveness to wireworms compared to spring wheat. Experimental plots were located in two commercial grain fields in Valier and Ledger, Montana, USA and the trials took place from May to August in 2015 and 2016. Wheat plants damaged by wireworms were recorded and their relative locations in wheat rows and adjacent trap crop rows within a plot were determined using destructive soil samples. In 2016, variable row spacing (0.25, 0.5, 0.75, and 1 m) between the trap crops (pea and lentil) and wheat was assessed. Shade house bioassays were conducted using potted pea, lentil, and wheat plants to support field trial results. Limonius californicus larvae, released at the center of each pot were sampled 4 and 10 days after sowing. Wheat intercropped with pea and lentil had significantly fewer damaged wheat plants. Wireworm numbers were lower in wheat intercropped with pea compared to the control for both locations and years. Shade house results corresponded with field results, with more wireworms collected from pea and lentil than wheat. In the spacing trials, wheat plant counts were also significantly higher when paired with pea and lentil, particularly at 0.5 m spacing. Regardless of inter-row spacing, significantly fewer wireworms were associated with wheat when intercropped with pea and lentil trap crops.     

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.     

Genetic identification of morphologically cryptic agricultural pests

1 Wireworms are the polyphagous larvae of click beetles and are well known as agricultural pests. Larvae of the genus Agriotes are internationally recognized as economically important pests of potato. Historically associated with crop damage after conversion of grassland, they are an increasing problem even in all-arable rotations.
2 Current studies of Agriotes ecology and behaviour, and consequently control and management, are seriously hampered by the lack of a means of reliably identifying larvae owing to morphological crypsis during this life-stage.
3 Here, sequence data at the mitochondrial 16SrRNA gene are presented for three species of wireworm: Agriotes obscurus, A. lineatus , and A. sputator. A novel terminal restriction fragment length polymorphism (T-RFLP) technique is described that identifies larvae of these species. This technique is shown to be both efficient and reliable. Interestingly, thus far the samples tested have yielded no A. lineatus. Implications for future study of wireworm ecology and control are discussed.