1000 resultados para ENTOMOLOGIA FORENSE
Resumo:
Parasitoid Hymenoptera (Insecta, Hymenoptera) collected in a cotton (Gossypium hirsutum L.) (Malvaceae) plantation at the municipal district of Ribeirão Preto, SP, Brazil. Parasitoid Hymenoptera were collected by using Moericke trap placed in a cotton plantation (Gossypium hirsutum L.) of the variety Delta Pine 90, during the period of February 23rd to April 3rd, 2001. A total of 16,166 specimens of parasitoids, belonging to eight superfamilies and 22 families, were collected. Encyrtidae, Trichogrammatidae, Mymaridae and Scelionidae were the most common families, being responsible for 45.14%, 19.11%, 14.33% and 6.57% of the total number of parasitoids collected, respectively. Other eigthteen families showed the relative frequency lower than 5%.
Resumo:
Revision of the genus Mecocephala Dallas, 1851 (Heteroptera, Pentatomidae). The genus Mecocephala Dallas, 1851 is revised, and some taxonomic and geographical distribution data are evaluated. The following species are considered to belong to this genus: M. acuminata Dallas, 1851 = M. holmbergi Pirán, 1969 syn. nov., M. curculionoides Pirán, 1959, M. bonariensis sp. nov., M. magna sp. nov., M. maldonadensis sp. nov., and M. zikani sp. nov.; their distribution is restricted to southern Neotropical Region. Other species, formerly placed in Mecocephala, are considered, respectively: M. rubripes Berg, 1894 incertae sedis, M. darwini Kirkaldy, 1909 incertae sedis, M. atra Bergroth, 1914 incertae sedis, Paramecocephala uruguayensis (Pirán, 1970) comb. nov., Paramecocephala fusca (Haglund, 1868) comb. nov. A key to the species is presented.
Resumo:
Parasitoid Hymenoptera collected in a soybean plantation (Glycine max (L.)) Merril (Fabaceae) at the municipal district of Nuporanga, SP, Brazil. Parasitoid Hymenoptera were collected by using Moericke trap placed in a soybean plantation (Glycine max (L.) Merril) (Fabaceae) of the variety Conquista, during the period of March 24th to April 7th, 2000. A total of 4,969 specimens of parasitoids, belonging to seven superfamilies and 15 families, were collected. Scelionidae, Encyrtidae, Aphelinidae and Trichogrammatidae were the most common families, being responsible for 41.66%, 19.42%, 11.19% and 7.35% of the total number of parasitoids collected, respectively. Other eleven families showed the relative frequency lower than 5%.
Resumo:
The Ichneumonidae (Hymenoptera) of the Estação Ecológica of the Universidade Federal de Minas Gerais, Belo Horizonte, with emphasis on the Pimplinae species. In one annual cycle 83,712 insects were captured, of which 2,339 were Ichneumonidae, belonging to 17 subfamilies; they were collected by a Malaise trap placed in a montane semidecidual seasonal forest, inside the campus. Among the collected ichneumonids there were 13 genera and 30 species of Pimplinae, of which Pimpla croceiventris was the most frequent species. The species richness of Pimplinae was greater in the ecological station in Belo Horizonte, MG than in other localities studied.
Resumo:
Restructure of the genus Deois Fennah; description of a new genus and new species (Homoptera, Cercopidae, Tomaspidinae). The genus Deois Fennah is reviewed and some changes in the taxonomy are introduced. The genus and its four subgenera are redefined, having now the following composition: 1) subgenus Deois (Deois) with: D. (D.) correntina (Berg, 1879), D. (D.) grandis Sakakibara, 1979, D. (D.) knoblauchii (Berg, 1879) (formerly in D. (Pandysia)), D. (D.) morialis (China & Myers, 1934), D. (D.) mourei Cavichioli & Sakakibara, 1994, D. (D.) piraporae Sakakibara, 1979, D. (D.) pseudoflavopicta (Lallemand, 1938) comb. nov. (formerly in Mahanarva) = D. (D.) similis Sakakibara, 1979 syn. nov., D. (D.) rubropicta Sakakibara, 1979, D. (D.) spinulata sp. nov., D. (D.) terrea (Germar, 1821), D. (D.) uniformis (Distant, 1909). 2) subgenus Deois (Pandysia) with: D. (P.) bergi sp. nov., D. (P.) crenulata sp. nov., D. (P.) schach (Fabricius, 1787) = Sphenorhyna transiens Walker, 1851 syn. nov.. 3) Deois (Fennahia) with: D. (F.) coerulea (Lallemand, 1924), D. (F.) flexuosa (Walker, 1851). 4) Deois (Acanthodeois) with: D. (A.) flavopicta (Stål, 1854), Deois (A.) incompleta (Walker, 1851). The genus Orodamnis Fennah, 1953 stat. nov. (formerly Deois (Orodamnis)) with: Orodamnis rhynchosporae (China & Myers, 1934) comb. nov. The genus Deoisella gen. nov. is described for: Deoisella fasciata sp. nov. (type species) and Deoisella picklesi (China & Myers, 1934) comb. nov.
Resumo:
Revision of the genus Paramecocephala Benvegnú, 1968 (Heteroptera, Pentatomidae). The Neotropical genus Paramecocephala Benvegnú, 1968 is revised based on morphological characters, particularly of the genitalia of both sexes. Formerly monobasic with P. foveata Benvegnú, 1968, type species, the genus received two species recently transferred from Mecocephala Dallas, 1851: M. fusca Haglund, 1868 and M. uruguayensis Pirán, 1970. Five new species are herein described: P. australis Frey-da-Silva & Grazia sp. nov., P. bachmanni Frey-da-Silva & Grazia sp. nov., P. bergrothi Frey-da-Silva & Grazia sp. nov., P. guianensis Frey-da-Silva & Grazia sp. nov. and P. subsolana Frey-da-Silva & Grazia sp. nov. Illustrations of the genitalia, a key to the species and a distribution map are provided.
Resumo:
The following nomenclatural changes are made: Amastris convoluta (Fabricius, 1781) comb. nov. (formerly Darnis; Hebetica); Amastris maculata Funkhouser, 1922 = Amastris fasciata Broomfield, 1976 syn. nov. = Amastris pseudomaculata Broomfield, 1976 syn. nov. = Amastris inermis Broomfield, 1976 syn. nov. = Amastris sakakibarai Broomfield, 1976 syn. nov.; Amastris elevata Funkhouser, 1922 = Amastris vismiae Haviland, 1925 syn. nov. = Amastris flavifolia Funkhouser, 1927 syn. nov.
Resumo:
A case of anomaly in Eulaema mimetica Moure (Hymenoptera, Apidae, Euglossinae). Legs deformations in a paratype male of Eulaema mimetica Moure, 1967, from Iquitos, PERU, are related for the first time.
Resumo:
A redescription of the genus Bruchopria and its two species, B. hexatoma Kieffer (female and male) and B. pentatoma Kieffer (male only) is presented. New record for B. hexatoma from Argentina is provided. Some aspects of diapriid biology with emphasis on their myrmecophilic evidence and association with ants are discussed. Scanning photographs of morphological structures are included.
Resumo:
Nymphal development of the predator Podisus nigrispinus (Dallas) fed with a susceptible (UFV 16) or an insect resistant soybean genotype (IAC 17) and with larvae of the prey Anticarsia gemmatalis Hübner (Lepidoptera, Noctuidae) reared on these genotypes, was evaluated. Survival and duration of each instar and of total nymphal stage, besides weight of nymphs at the beginning of each instar and of adults of P. nigrispinus soon after emergence, were also evaluated. Nymphal survival of this predator was similar with both genotypes (64.41% for the UFV 16 and 72.88% for the IAC 17). Duration of second and fourth instars for nymphs that originated females, of fourth instar for those that originated males, of the nymphal period for males (20.21 and 17.94 days) and females (19.76 and 18.19 days) was longer on the IAC 17 than on the UFV 16. Weight of third instar nymphs (3.12 mg and 2.42 mg) for those that originated males and of fifth instar (26.20 mg and 23.86 mg) for those that originated females and female weight after emergence (65.76 mg and 58.68 mg) was lower with the IAC 17 than with the UFV 16. Sex ratio of P. nigrispinus was not affected by the resistant soybean IAC 17.
Resumo:
Six species of Anisepyris Kieffer, 1905 were collected in Cachoeira da Fumaça (Alegre) and Forno Grande (Castelo) State Parks. Two of them are already known: Anisepyris lobatus Santos & Azevedo, 2000 and Anisepyris rectus Santos & Azevedo, 2000. Other four are described as new: Anisepyris attenuatus sp. nov., Anisepyris divisus sp. nov., Anisepyris inconspicuus sp. nov., and A. rotundus sp. nov.; each new species is illustrated. Two uncommon characters for Anisepyris, such as an inconspicuous anterior carina of the pronotum, and a lower mesopleural fovea partially open on the lower margin were observed being both the characters found in A. inconspicuus sp. nov. and only the first character in A. attenuatus sp. nov.
Resumo:
The objectives of this research were to evaluate leaf consumption and the developmental time of the larvae of Erynnyis ello (L., 1758) (Lepidoptera, Sphingidae) reared on cassava, in order to obtain information for the integrated management of this pest. The larvae were reared on excised cassava leaves in Petri dishes and later in gerbox, and kept in chambers at 24 ± 2 ºC and 75 ± 10% RH. The total leaf area consumed by the larva to complete its development was 589.67 cm²; each of the five instars consumed, respectively: 1.89 cm²; 5.74 cm²; 17.48 cm²; 76.66 cm²; and 487.90 cm². The consumption by the first three instars was insignificant, and did not reach 5% altogether; the 4th represented 13%; the 5th presented a consumption significantly higher, about 82.7%. The total time for the larval development was 22.61 days, and the duration for each of the five larval instar was, respectively: 4.35; 3.19; 3.32; 4.52; and 4.94 days. The pre-pupal period lasted 2.29 days. Since the highest consumption is by the 5th instar larva, the control should be applied before this age to avoid heavier damages to the cassava crop.
Resumo:
The flea, Myodopsylla wolffsohni wolffsohni (Rothschild, 1903), had been recorded for the first time in the State of Paraná in 1940, on the bat, Myotis levis (I. Geoffroy, 1824). Previously, this species of flea had only been recorded on Myotis nigricans, in the Amazonian region. This is the second record of M. w. wolffsohni on M. nigricans in Brazil, and the first in the State of Paraná. Although this flea has been found on undetermined Chiroptera in the State of Santa Catarina, the present record represents the meridional limit of geographic distribution for the infestation on M. nigricans.
Resumo:
The subgenus Centris (Aphemisia) Ayala: complementary notes and description of a new species (Hymenoptera, Apoidea). Centris (Aphemisia) Ayala, 2002 is redescribed pointing out some others important distinctive characters. The nominal species designated by Ayala as the type species, Centris plumipes Smith, 1854, is preocupied by Centris plumipes (Fabricius, 1781) originaly described in Apis Linnaeus. Being so, Centris xanthosara nom. nov. is proposed to replace Centris plumipes Smith, 1854 non Centris plumipes (Fabricius, 1781). Two other species are considered to belong in this subgenus: Centris (Aphemisia) lilacina Cockerell, 1919, and Centris (Aphemisia) plumbea sp. nov., from Tingo Maria, Peru. A key for the species, illustrations, and geographical distribution are also added.
Resumo:
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.