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.
In estimating the population abundance by the mark-recapture method using male-attractant pheromone traps, the release of sterile males is preferable, because they do not increase the reproductive ...rate of wild females by increasing the mating rate. We estimated the influence of gamma radiation on males of the sugarcane click beetle Melanotus okinawensis Ôhira (Coleoptera: Elateridae) to determine an appropriate dose of gamma radiation in laboratory and field experiments. The hatchability of eggs was examined for 0, 50, 70, 90, and 150 Gy. No hatchings were observed in eggs laid by females which mated with males treated with doses of 70, 90 and 150 Gy. The longevity of adults in the laboratory was estimated with 0, 30, 50, 70, 90, 150, and 200 Gy. Analysis by the proportional hazard model indicated that irradiation significantly reduces the survival rate in the laboratory even if the dose is 30 Gy. Mean dispersal distance in the field was estimated with 0, 50, 90, and 150 Gy. Three hundred marked beetles for each dose were released at the center of Ikei Island on 1 and 3 April 2003. The estimates were 274, 219, 192, and 289 m, respectively, and we could not detect a significant influence of irradiation on the mean dispersal distance. Field survival rates were estimated using Jolly-Seber, Yamamura, and Yamamura B methods at Okinawa Prefectural Experiment Station in Naha for two doses of irradiation, 0 and 90 Gy; we could not detect significant differences between the two survival rates. The mortality added in the field was estimated to be much greater than the mortality caused by irradiation when we focus on the experiment within 12 days after release, if the dose of irradiation is lower than 90 Gy. It was therefore concluded that 90 Gy will be an appropriate dose for preparing sterile males to estimate population abundance and survival rate in the field within 12 days after release.
The genus Chalcolepidius is revised. Type specimens of 65 nominal species, except C. costatus Pjatakowa, 1941, C. fleutiauxi Pjatakowa, 1941 and C. viriditarsus Schwarz, 1906, are examined. Eighty ...five species are studied, of which 34 are synonymyzed and 12 new species described; three species, C. alicii Pjatakowa, 1941, C. haroldi Candèze, 1878 and C. unicus Fleutiaux, 1910, formely included in this genus, are not congeneric and are removed; C. validus Candèze, 1857 is revalidated. The genus is now formed by 63 species. Redescriptions, illustrations and a key for the examined species, and a cladistic analysis for groups of species are also included. New synonyms established: C. apacheanus Casey, 1891 = C. simulans Casey, 1907 syn. nov. = C. acuminatus Casey, 1907 syn. nov. = C. nobilis Casey, 1907 syn. nov.; C. approximatus Erichson, 1841 = C. aztecus Casey, 1907 syn. nov. = C. niger Pjatakowa, 1941 syn. nov.; C. attenuatus Erichson, 1841 = C. cuneatus Champion, 1894 syn. nov. = C. tenuis Champion, 1894 syn. nov.; C. aurulentus Candèze, 1874 = C. candezei Dohrn, 1881 syn. nov. = C. grossheimi Pjatakowa, 1941 syn. nov.; C. bomplandii Guérin, 1844 = C. humboldti Candèze, 1881 syn. nov.; C. chalcantheus Candèze, 1857 = C. violaceous Pjatakowa, 1941 syn. nov.; C. cyaneus Candèze, 1881 = C. scitus Candèze, 1889 syn. nov. = C. abbreviatovittatus Pjatakowa, 1941 syn. nov.; C. desmarestii Chevrolat, 1835 = C. brevicollis Casey, 1907 syn. nov.; C. gossipiatus Guérin, 1844 = C. erichsonii Guérin-Méneville, 1844 syn. nov. = C. lemoinii Candèze, 1857 syn. nov.; C. inops Candèze, 1886 = C. murinus Champion, 1894 syn. nov.; C. jansoni Candèze, 1874 = C. mucronatus Candèze, 1889 syn. nov.; C. lacordairii Candèze, 1857 = C. exquisitus Candèze, 1886 syn. nov. = C. monachus Candèze, 1893 syn. nov.; C. lenzi Candèze, 1886 = C. behrensi Candèze, 1886 syn. nov.; C. oxydatus Candèze, 1857 = C. jekeli Candèze, 1874 syn. nov.; C. porcatus (Linnaeus, 1767) = C. peruanus Candèze, 1886 syn. nov. = C. flavostriatus Pjatakowa, 1941 syn. nov. = C. herbstii multistriatus Golbach, 1977 syn. nov.; C. rugatus Candèze, 1857 = C. amictus Casey, 1907 syn. nov.; C. smaragdinus LeConte, 1854 = C. ostentus Casey, 1907 syn. nov. = C. rectus Casey, 1907 syn. nov.; C. sulcatus (Fabricius, 1777) = C. herbstii Erichson, 1841 syn. nov; C. virens (Fabricius, 1787) = C. perrisi Candèze, 1857 syn. nov.; C. virginalis Candèze, 1857 = C. championi Casey, 1907 syn. nov.; C. viridipilis (Say, 1825) = C. debilis Casey, 1907 syn. nov.; C. webbi LeConte, 1854 = C. sonoricus Casey, 1907 syn. nov.; C. zonatus Eschscholtz, 1829 = C. longicollis Candèze, 1857 syn. nov. New species described: C. albisetosus sp. nov. (Ecuador), C. albiventris sp. nov. (Mexico: Veracruz), C. copulatuvittatus sp. nov. (Venezuela), C. extenuatuvittatus sp. nov. (Venezuela), C. fasciatus sp. nov. (Mexico: Durango), C. ferratuvittatus sp. nov. (Ecuador), C. proximus sp. nov. (Mexico: Sinaloa), C. serricornis sp. nov. (Mexico: Veracruz), C. spinipennis sp. nov. (Mexico: Veracruz), C. supremus sp. nov. (Venezuela), C. truncuvittatus sp. nov. (Mexico: Tamaulipas) and C. virgatipennis sp. nov. (Mexico: Durango). Redescribed species: C. angustatus Candèze, 1857, C. apacheanus Casey, 1891, C. approximatus Erichson, 1841, C. attenuatus Erichson, 1841, C. aurulentus Candèze, 1874, C. bomplandii Guérin-Méneville, 1844, C. boucardi Candèze, 1874, C. chalcantheus Candèze, 1857, C. corpulentus Candèze, 1874, C. cyaneus Candèze, 1881, C. desmarestii Chevrolat, 1835, C. dugesi Candèze, 1886, C. erythroloma Candèze, 1857, C. eschscholtzi Chevrolat, 1833, C. exulatus Candèze, 1874, C. fabricii Erichson, 1841, C. forreri Candèze, 1886, C. fryi Candèze, 1874, C. gossipiatus Guérin-Méneville, 1844, C. inops Candèze, 1886, C. jansoni Candèze, 1874, C. lacordairii Candèze, 1857, C. lafargi Chevrolat, 1835, C. lenzi Candèze, 1886, C. limbatus (Fabricius, 1777), C. mexicanus Castelnau, 1836, C. mniszechi Candèze, 1881, C. mocquerysii Candèze, 1857, C. morio Candèze, 1857, C. obscurus Castelnau, 1836, C. oxydatus Candèze, 1857, C. porcatus (Linnaeus, 1767), C. pruinosus Erichson, 1841, C. rodriguezi Candèze, 1886, C. rostainei Candèze, 1889, C. rubripennis LeConte, 1861, C. rugatus Candèze, 1857, C. silbermanni Chevrolat, 1835, C. smaragdinus LeConte, 1854, C. sulcatus (Fabricius, 1777), C. tartarus Fall, 1898, C. validus Candèze, 1857, reval., C. villei Candèze, 1878, C. virens (Fabricius, 1787), C. virginalis Candèze, 1857, C. viridipilis (Say, 1825), C. webbi LeConte, 1854, C. zonatus Eschscholtz, 1829.
By the example of 14 coleopterous insect families, namely Gyrinidae, Haliplidae, Noteridae, Dytiscidae, Carabidae, Hydrophilidae, Staphylinidae, Lucanidae, Trogidae, Scarabaeidae, Elateridae, ...Alleculidae, Tenebrionidae, and Chrysomelidae, regularities and the basic sources of formation of the most typical landscapecoenotic complexes in the Northwest Caucasus are discussed. The total number of the species included in the material analyzed amounts to about 2000. The maximal species diversity (854 species) is registered for the deciduous forests and dry open woodlands. In total, 11 types of the chorological complexes and distributional ranges (chorotypes) of the regional beetle fauna are distinguished. Significant concordance of the chorologic patterns in some groups of beetles is established. In this respect, Carabidae and Tenebrionoidea seem to be the closest on the one hand, and also Elateridae and Scarabaeoidea, on the other. The zonal fauna of the Northwest Caucasus is formed basically by species possessing Boreal ranges, while the azonal fauna, predominantly by species with the Ancient Mediterranean ranges. Allocation of coleopterous insects within regional zoochorones is investigated as well. It is established, that in different zoochorones of the upland part of the region the majority of coenofaunas show significant similarity of the arealogical pattern, even though being composed frequently by different taxa. The fauna of agrarian landscapes of the Northwest Caucasus is also examined. It includes 382 beetle species. The overwhelming majority of them belongs to the ground beetles (229 species), leaf beetles (78), and Scarabaeoidea (30). This fauna reveals the maximal similarity with the coenofaunas of the lowland steppe and meadows. It is established that the major role in formation of the agrocenoses beetle fauna belongs to the natural plain and upland steppe and treeless fields, foothill broad-leaf forests and open woodlands, and also to the floodplain and lowland forests. The bulk of the species occurring in the agrocenoses possesses wide ranges, predominantly of the Boreal type. Some peculiarities of the regional endemism are discussed as well.
Carbon and nitrogen isotope ratios in consumer tissues can be used to analyse the diet and trophic level of soil animals. However, life history traits may significantly influence stable isotope ...patterns. We evaluated in a series of experiments how stable isotope ratios of carbon (
13C/
12C) and nitrogen (
15N/
14N) at natural abundance can be used to study the diet and trophic position of long-lived macro-invertebrates, elaterid larvae, which are major below-ground herbivores. Small, but significant differences in
δ
13C signatures were found between the larvaes’ anterior and posterior body segments, whereas exuvia reflected the body's overall isotopic composition. The species-specific trophic shift (±SE) in
δ
15N for
Agriotes obscurus and
Agriotes sputator (1.62±0.24‰ and 1.08±0.27‰, respectively) was significantly lower than “mean enrichment estimates” reported in the literature, showing the limited applicability of such generalised estimates in studies of invertebrate trophic ecology. To avoid false-positive assignments to two trophic levels due to variation in
δ
15N values, a minimum sample size of three and five individuals for
A. obscurus and
A. sputator, respectively, was needed to reduce this risk to below
α=5%. Keeping elaterid larvae for up to 128 days without food did not affect their isotopic signatures, in contrast to previous studies on starving animals. Switching wireworms to isotopically different diets induced changes in their isotopic signatures within 2 weeks. Changes, however, were significant only when the isotopic difference between diets was large. We conclude that experimental studies evaluating how specific life history traits affect stable isotope signatures in consumers have to precede any interpretation of stable isotope data gathered in the field.
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