Diversidade de Pentatomoidea (Hemiptera, Heteroptera) em três fragmentos de Mata Atlântica no sul de Santa Catarina

A composição e a variação sazonal da fauna de Pentatomoidea (Hemiptera) foi avaliada entre setembro de 2005 e agosto de 2006 em três fragmentos de Mata Atlântica na região sul de Santa Catarina (Brasil): Parque Ecológico José Milanese (Criciúma, 28º41'23''S, 49º25'55''W), Parque Ecológico de Maracajá (Maracajá, 28º52'51''S, 49º27'59''W) e Balneário Morro dos Conventos (Araranguá, 28º56'05''S, 49º21'47''W). Foram realizadas coletas mensais ao longo de trilhas nas três áreas, utilizando guarda-chuva entomológico e rede de varredura para amostrar nas bordas de mata. Para um esforço amostral de 108 horas foram coletados 595 indivíduos, distribuídos em 4 famílias, 29 gêneros e 49 espécies. Pentatomidae foi a família mais abundante (82,69%) seguida de Cydnidae (15,97%), Scutelleridae (0,84%) e Tessaratomidae (0,50%). Pentatomidae também apresentou a maior riqueza com 37 espécies. As espécies mais abundantes foram Mormidea notulifera Stål, 1860, Oebalus ypsilongriseus (De Geer, 1773), Arvelius albopunctatus (De Geer, 1773), Edessa subrastrata Bergroth, 1891, Galgupha schulzii (Fabricius, 1781) e Agroecus scabricornis (Herrich-Schäffer, 1844). O período de maior captura foi entre o final da primavera e início do outono, representando 71,76% do total coletado. O Parque do Maracajá apresentou abundância e riqueza sgnificativamente maiores do que as demais áreas. Este estudo representa o primeiro inventário da diversidade de Pentatomoidea em habitats naturais no estado de Santa Catarina.

Vespas sociais (Hymenoptera, Vespidae, Polistinae) de floresta pluvial Amazônica de terra firme em Caxiuanã, Melgaço, Pará

As vespas sociais são notáveis por sua organização social complexa, arquitetura elaborada dos ninhos, e por seu papel em ecossistemas terrestres como predadores de outros insetos e artrópodes. O número de inventários de vespas sociais no Brasil ainda é pequeno, assim como os esforços para padronização dos protocolos de coleta, dificultando a comparação entre os resultados obtidos. A composição e a riqueza das vespas sociais na Floresta Nacional de Caxiuanã, Melgaço, PA, foram avaliadas através de um inventário estruturado numa parcela quadrada de 25 km² de floresta de terra firme. Os métodos de coleta empregados foram a "busca ativa por indivíduos e colônias em trilhas de 1.000m" e "armadilhas de Malaise". Foram registradas 65 espécies de vespas sociais pertencentes a 12 gêneros. Agelaia fulvofasciata (Deeger, 1773) e Angiopolybia pallens (Lepeletier, 1836) foram as espécies mais frequentes na área em ambos os métodos. Busca ativa apresentou um melhor desempenho quanto à descoberta de espécies de vespas sociais (63) do que armadilha de Malaise (26). O levantamento representou um incremento de 21 espécies à lista obtida anteriormente para Caxiuanã e de um novo registro para o estado do Pará (Polybia brunnea (Curtis, 1844)).

Another color morph of Sporophila Seedeater from the capuchinos group (Aves, Emberizidae)

The genus Sporophila (Cabanis, 1844) unites about 30 species of small seedeaters that predominantly inhabit open or semi-open areas in the Neotropical region. The taxonomy of this group is based on morphological studies from collected male specimens. The dynamic spatial and temporal variation in the male plumage and lack of knowledge of their vocalizations make it difficult to properly diagnose some species even today, so these two aspects account for the existing taxonomic dilemmas involving Sporophila. During a four-year field study, we investigated the natural history of a breeding population of Sporophila melanogaster (Pelzeln, 1870). This is an endemic species in Brazil, which reproduces in the high-altitude grasslands of the Atlantic Forest biome. We found four male specimens with clearly diagnosable plumage, distinct from the typical form of the species. Here we describe this previously unreported plumage form. Based on the evaluation of habitat use, vocalization, and reproductive behavior, we tested two hypotheses regarding its taxonomic status. We concluded that this is another case of an intra-specific color morph within the seedeaters of the "capuchinos" group.

New records, distribution and status of six seabird species in Brazil

Distribution records of poorly-known species are currently the most explored theme in the Brazilian seabird literature. If properly evaluated, this kind of information can improve our knowledge on distribution, migration and status of occurrence of these species. In this note we present new records for six species of poorly-known seabirds in the Brazilian coast, reviewing distribution records and defining their status of occurrence in the country. We consider Chionis albus (Gmelin, 1789) a pseudo-vagrant in Brazil and define its status as a scarce seasonal visitor from southern South America. We present the first records of Leucophaeus atricilla (Linnaeus, 1758) for Trindade Island, and of Leucophaeus pipixcan (Wagler, 1831) for the state of Rio Grande do Sul, and determined that the former is a vagrant in eastern Brazil and the latter a vagrant across the country. Anous stolidus (Linnaeus, 1758) is a vagrant in southernmost Brazil. We were unable to determine if records of Chlidonias niger (Linnaeus, 1758) for Brazil and southern South America refer to vagrancy or pseudo-vagrancy. Additionally, we verified the occurrence of breeding individuals of Anous minutus Boie, 1844 on Martin Vaz Island and confirmed that there is no evidence of breeding on neighboring Trindade Island.

Taxonomy, distribution and population structure of invasive Corbiculidae (Mollusca, Bivalvia) in the Suquía River basin, Córdoba, Argentina

Invasive species are one of the most significant causes of biodiversity loss and changes in ecosystem services, which underlines the importance of their detection and their study. The Asian clams (Corbiculidae) are invasive organisms that accidentally entered the La Plata River, Argentina, presumably in the 1960s. The objectives of the present study were to identify the corbiculid species and to determine their distribution at several locations along the Suquía River basin, an extended area in central Argentina. In addition, population structure was evaluated monthly during one year, at a site in the city of Córdoba that is characterized by high human influence. The presence of Corbicula fluminea (Müller, 1774) and Corbicula largillierti (Philippi, 1844) in the Suquía River basin is reported for the first time. The former species was found only in a lentic environment (San Roque reservoir), while the latter was also found along the tributary rivers and brooks of the basin. Corbicula largillierti showed variations in average density between the different sites and also in biomass and size classes throughout the study period at the site at Córdoba city. The relative composition of the sediments, flow fluctuation and human pollution may be responsible for the observed differences.

Observações sobre os Ixodideos da Republica Argentina

Ixodidae of the Argentine Republic are studied by the Author based on 71 lots of material, sent by Prof. Salvador Mazza, comprising 13 different species, two of which are found in Argentine territory: Haemaphysalis kochi Arag. and Amblyomma parvitarsum Nn. The author admits the existence in Argentina of 23 species of Ixodidae, but such number may still increase along with the development of the studies on the subject. In this paper, the Ornithodoros classified by Barbará and Dios as Ornithodoros turicata, is sunk by the Author in synonymy with O. rostratus Arag. not merely on the strength of the material at his disposal, but also by the plates published by the Argentine authors. The following species are also placed in synonymy: Amblyomma altiplanum Dios, 1917 (= Amblyomma parvitarsum Nn., 1899), Amblyomma concolor, Nn., 1899 (=Amblyomma auriculare Conil, 1877) Amblyomma furcula Donitz, 1907 (= Amblyomma neumani Ribaga, 1902). In the Author's opinion Amblyomma striatum C. L. Koch, 1844 and Amblyomma fossum Nn. are distinct species, so that the same Amblyomma ovale for both should no longer subsist as L. C. Robinson proposes. The Author, moreover, shows his doubts upon the existence in Argentine of Aponomma laeve, Nn., 1899 and Dermacentor triangulus Nn., 1899, as they have not been seen any more and in South-America no representatives of the genera Aponomma and Dermacentor are known.

Notas de ixodologia: V - A propósito da validade de algumas espécies do gênero Amblyomma do continente americano (Acari: Ixodídoe)

a) The species Amblyomma tapiri Tonelli Rondelli, 1937 and Amblyomma finitimum Tonelli Rondelli, 1937 are synonymous with Amblyomma cajennense Fabricius, 1787. Both species are based in differences of size, colour, punctations and form of the dorsal shield, presence or absence of ventral plates, size, form and direction of the spine of coxa IV. Such differences prouved to be only variations frequently observed in large lots or in cultures of Amblyomma cajennense. The revalidation of Koch's species Amblyomma tenellum Koch, 1844 and Amblyomma mixtum Koch, 1844 proposed by TONELLI RONDELLI as also of Amblyomma sculptum Berlese, 1888 and Amblyomma versicolor Nuttal et Warburton, 1908 cannot be accepted by the same reasons. b) Amblyomma beccari Tonelli Rondelli, 1939 and Amblyomma latepunctatum Tonelli Rondelli, 1939 are cospecific with Amblyomma scalpturatum Neumann, 1899 the same being true for Amblyomma myrmecophagium Schulze, 1935 and for Amblyomma brasiliense var. guianense Floch et Abonnenc, 1940, as previously stated. c) Amblyomma tasquei Floch et Abonnenc, 1940 is a good species but synonym with Amblyomma romitii Tonelli Rondelli, 1939 which has priority. d) Amblyomma curruca Schulze, 1936 is a synonym of Amblyomma parvum Aragão, 1908. e) Amblyomma deminutivum Neumann, 1899 represents a variation of Amblyomma dissimile Koch, 1844, a species whose internal spine of coxa IV may be poorly developed or even absent. f) Amblyomma nigrum Tonelli Rondelli, 1939 prouved to be synonym with Amblyomma paccae Aragao, 1911 the type representing a blackish specimen of the later species. g) Amblyomma brimonti Neumann, 1913 is a synonym of Amblyomma humerale Koch, 1844.

Notas de ixodologia: IX. O complexo ovale do gênero Amblyomma

It was impossible to confirm either WARBUTON's conservative nor TONELLI RONDELLI's opposite belief on the number of valid species after studying many lots of ticks of the ovale group, mainly from Brazil. Two species are recognized: Amblyomma ovale Koch, 1844 and Amblyomma aureolatum (Pallas, 1772), corresponding respectively to A. fossum Neumann, 1898 and A. stratum Koch, 1844. A list of synonyms is presented. Both species are redescribed and intraspecific morphological variation show to be the cause of the multiplication of species by those working with insufficient material. Color plates of both species are presented and hosts and localities of captures are recorded.

The genus lobatostoma (Trematoda: Aspidocotylea) in the pacific coast of South America, with description of Lobatostoma veranoi new species, parasite of Menticirrhus ophycephalus (Teleostei: Sciaenidae)

The presence of three aspidocotyleans trematodes in marine fishes from Perú and Chile is reported. One of them, Lobatostoma veranoi from the intestine of Menticirrhus ophicephalu (Sciaenidae) is considered a new species. Distinct characteristcs of the new species are:a cirrus sac smaller than the pharynx; tail overlapping posteriorly the ventral disk; testis in the last third of the body and the presence of 64-66 marginal alveoli. The two other species are Lobatostoma pacificum Manter, 1940 found in Trachinotus paitensis Cuvier, 1830 from Perú and Chile and Lobatostoma Anisotremum Oliva & Carvajal, 1984 from the intestine of Anisotremus scapularis (Tschudi, 1844) from Perú.

Neotropical planorbid snails with apertural lamellae: I. Biomphalaria helophila (Orbigny, 1835)

A definition of Biomphalaria helophila (Orbigny, 1835) is presented, based on examination of the shell and reproductive system of topotypic specimens and extended to a number of samples from other localities. The following nominal species and subspecies, collected from type localities, proved junior synonyms of B. helophila: Planorbis albicans Pfeiffer, 1839; Planorbis dentatus Gould, 1844; Planorbis dentiferus CB Adams, 1845; Planorbis dentiferus edentatus CB Adams, 1851; Planorbis dentiens Morelet, 1849; Planorbula dentiens edentula Fischer & Crosse, 1880; Planorbis stagnicola Morelet, 1851; and Tropicorbis shimeki FC Baker, 1945. B. helophila was also identified in samples from Costa Rica, Guatemala, Haiti, Dominican Republic, Puerto Rico and Barbados.

Review of the genus Chalcolepidius Eschscholtz, 1829 (Coleoptera, Elateridae, Agrypninae)

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.