975 resultados para Geographical Distribution


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BACKGROUND: Mitochondrial DNA sequencing increasingly results in the recognition of genetically divergent, but morphologically cryptic lineages. Species delimitation approaches that rely on multiple lines of evidence in areas of co-occurrence are particularly powerful to infer their specific status. We investigated the species boundaries of two cryptic lineages of the land snail genus Trochulus in a contact zone, using mitochondrial and nuclear DNA marker as well as shell morphometrics. RESULTS: Both mitochondrial lineages have a distinct geographical distribution with a small zone of co-occurrence. In the same area, we detected two nuclear genotype clusters, each being highly significantly associated to one mitochondrial lineage. This association however had exceptions: a small number of individuals in the contact zone showed intermediate genotypes (4%) or cytonuclear disequilibrium (12%). Both mitochondrial lineage and nuclear cluster were statistically significant predictors for the shell shape indicating morphological divergence. Nevertheless, the lineage morphospaces largely overlapped (low posterior classification success rate of 69% and 78%, respectively): the two lineages are truly cryptic. CONCLUSION: The integrative approach using multiple lines of evidence supported the hypothesis that the investigated Trochulus lineages are reproductively isolated species. In the small contact area, however, the lineages hybridise to a limited extent. This detection of a hybrid zone adds an instance to the rare reported cases of hybridisation in land snails.

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Recently, genetic evidence supported the existence of a new species of the genus Pollicipes from the Cape Verde Islands, previously considered a population of P. pollicipes. However, P. pollicipes was not sampled at its southern limit of distribution (Dakar, Senegal), which is geographically separated from the Cape Verde Islands by about 500 km. Herein we describe Pollicipes caboverdensis sp. nov. from the Cape Verde Islands and compare its morphology with the other three species of Pollicipes: P. pollicipes, P. elegans and P. polymerus. Pollicipes pollicipes was sampled at both the middle (Portugal) and southern limit (Dakar, Senegal) of its geographical distribution. The genetic divergence among and within these two regions and Cape Verde was calculated through the analysis of partial mtDNA CO1 gene sequences. Pollicipes caboverdensis sp. nov. has a single whorl of capitular plates below the subrostrum, peduncular scales pointing up toward the capitulum and multi-articulate caudal appendages (all characters shared with P. pollicipesand P. elegans), reddish-orange capitular plates (large specimens), a single rostral median latus between the median latus and the rostrolatus (both characters shared with P. elegans), and uniquely possesses peduncular scales that are approximately the same width as height. The genetic distance between the Cape Verde population and the Senegal and Portugal populations is 13–14%, whilst between Senegal and Portugal it is < 1%.

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Taxonomic study of Leschenaultia Robineau-Desvoidy (Diptera, Tachinidae). The genus Leschenaultia Robineau-Desvoidy, 1830 is redescribed. Two genera are considered as its junior synonyms: Echinomasicera Townsend, 1915 syn. nov. and Parachaetopsis Blanchard, 1959 syn. nov. Thirty two especies are treated, as follows: 18 described as new, Leschenaultia aldrichi, sp. nov. (Brazil, Santa Catarina), L. arnaudi sp. nov. (Haiti, La Salle), L. bergenstammi sp. nov. (Peru, San Martin), L. bessi sp. nov. (Brazil, Santa Catarina), L. bigoti sp. nov. (Peru, Huanuco), L. blanchardi sp. nov. (Equador, Cuenca), L. braueri sp. nov. (Brazil, Mato Grosso), L. brooksi sp. nov. (Brazil, Rio de Janeiro), L. coquilletti sp. nov. (Brazil, Santa Catarina); L. cortesi sp. nov. (Venezuela, Maracay), L. currani sp. nov. (Brazil, São Paulo), L. loewi sp. nov. (Mexico, Vera Cruz), L. macquarti sp. nov. (U. S. A., Arizona), L. reinhardi sp. nov. (Canada, Quebec), L. sabroskyi sp. nov. from (U. S. A., California), L. schineri sp. nov. (U. S. A., California), L. thompsoni sp. nov. (Mexico, Mexico City), L. townsendi sp. nov. (Mexico, Puebla), and 14 known species, for these, diagnoses are given: L. adusta (Loew, 1872); L. americana (Brauer & Bergenstamm, 1893); L. bicolor (Macquart, 1846) = L. fusca (Townsend, 1916) syn. nov.; = Parachaetopsis proseni Blanchard, 1959 syn. nov.; L. ciliata (Macquart, 1848); L. exul (Townsend, 1892); L. fulvipes (Bigot, 1887); L. grossa Brooks, 1947; L. halisidotae Brooks, 1947; L. hospita Reinhard, 1952; L. hystrix (Townsend, 1915) comb. nov., L. jurinioides (Townsend, 1895); L. leucophrys (Wiedemann, 1830) = Leschenaultia latifrons (Walker, 1852) syn. nov. = Parachaeta nigricalyptrata (Macquart, 1855) syn. nov.; L. montagna (Townsend, 1912); L. nuda Thompson, 1963. One species was not examined, Leschenaultia nigrisquamis (Townsend, 1892), and two were not recognized, L. trichopsis (Bigot, 1887) and L. hirta Robineau-Desvoidy, 1830. Keys for Nearctic and Neotropical species (only for males) are provided, as well as geographical distribution and illustrations for each species.

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The genus Callideriphus Blanchard, 1851 (Coleoptera, Cerambycidae, Heteropsini). The genus Callideriphus comprises only two species: C. grossipes Blanchard, 1851 (type species) and C. tucumanus sp. nov. (Argentina, Tucumán). The type locality of C. grossipes had been originally indicated as Chile, but it is supposedly considered erroneous. Its distribution, actually, extends from Southeastern Brazil up to Argentina, along the Atlantic Forest. This species is extremely variable in regard to its coloration and elytral punctation. Two subspecies are recognized: C. grossipes grossipes Blanchard, 1851 (BRAZIL: Minas Gerais, Espírito Santo, São Paulo, Paraná, Santa Catarina) and C. grossipes flavipennis Melzer, 1934 (BRAZIL: Santa Catarina, Rio Grande do Sul; ARGENTINA: Chaco, Entre Ríos, Buenos Aires). Four intermediate forms are recorded and commented. Redescription and a key to species are added. Nomenclatural changes: Callideriphus grossipes grossipes Blanchard, 1851 = C. grossipes var. brasliensis Melzer, 1923 syn. nov. = C. rubricollis Melzer, 1934 syn. nov.; Callideriphus grossipes flavipennis Melzer, 1934 stat nov. = C. signaticollis Melzer, 1934 syn. nov.

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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.

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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.

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Systematics, phylogeny and geographical distribution of the South American species of Centris (Paracentris) Cameron, 1903, and Centris (Penthemisia) Moure, 1950, including a phylogenetic analysis of the "Centris group" sensu Ayala, 1998 (Hymenoptera, Apoidea, Centridini). A cladistic analysis with the objective of testing the hypothesis of monophily of Centris (Paracentris) Cameron, 1903, and of studying its phylogenetic relationships with the other subgenera that belong to the Centris group, sensu Ayala, 1998, and the relationships among the species that occur in South America, is presented. Centris (Paracentris) is a group of New World bees of amphitropical distribution, especially diversified in the Andes and in the xeric areas of South and North America. Thirty-one species were included in the analysis, four considered as outgroup, and 49 characters, all from external morphology and genitalia of adult specimens. Parsimony analyses with equal weights for the characters and successive weighting were performed with the programs NONA and PAUP, and analyses of implied weighting with the program PeeWee. The strict consensus among the trees obtained in all the analyses indicates that C. (Paracentris), as previously recognized, is a paraphyletic group. In order to eliminate that condition, the subgenera C. (Acritocentris), C. (Exallocentris) and C. (Xerocentris), all described by SNELLING (1974) are synonymized under C. (Paracentris). The subgenus C. (Penthemisia) Moure, 1950, previously considered a synonym of C. (Paracentris), is reinstated, but in a more restricted sense than originally proposed and with the following species: Centris brethesi Schrottky, 1902; C. buchholzi Herbst, 1918; C. chilensis (Spinola, 1851), C. mixta mixta Friese, 1904, and C. mixta tamarugalis Toro & Chiappa, 1989. Centris mixta, previously recognized as the only South American species of the subgenus C. (Xerocentris), a group supposedly amphitropical, came out as the sister-species of C. buchholzi. The following South American species were recognized under Centris (Paracentris): Centris burgdorfi Friese, 1901; C. caelebs Friese, 1900; C. cordillerana Roig-Alsina, 2000; C. euphenax Cockerell, 1913; C. flavohirta Friese, 1900; C. garleppi (Schrottky, 1913); C. klugii Friese, 1900; C. lyngbyei Jensen-Haarup, 1908; C. mourei Roig-Alsina, 2000; C. neffi Moure, 2000; C. nigerrima (Spinola, 1851); C. toroi sp. nov.; C. tricolor Friese, 1900; C. unifasciata (Schrottky, 1913), and C. vogeli Roig-Alsina, 2000. The relationships among the subgenera of the "Centris group" were: (Xanthemisia (Penthemisia (Centris s. str. - Paracentris))). Centris xanthomelaena Moure & Castro 2001, an endemic species of the Caatinga and previously considered a C. (Paracentris), came out as the sister group of C. (Centris) s. str. A new species of C. (Paracentris) from Chile is described: Centris toroi sp. nov. Lectotypus designations and redescriptions are presented for Centris burgdorfi, C. caelebs, C. lyngbyei, C. tricolor, C. autrani Vachal, 1904 and C. smithii Friese, 1900. New synonyms proposed: C. buchholzi Herbst, 1918 = Centris wilmattae Cockerell, 1926 syn. nov.; C. caelebs Friese, 1900 = Paracentris fulvohirta Cameron, 1903. The female of C. vogeli Roig-Alsina, 2000 and the male of C. xanthomelaena are described.

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The genus Anthidium Fabricius in the South America: key for the species, descriptive notes, and geographical distribution (Hymenoptera, Megachilidae, Anthidiini). The Anthidiini, in South America, is represented by a single genus Anthidium Fabricius, 1804 (type-species: Apis manicata Linnaeus, 1758). Thirty nine species are treated in this paper, as follows: Anthidium alsinai Urban, 2001; A. andinum Joergensen, 1912; A. anurospilum Moure, 1957 nom. reval. (formerly = A. espinosai Ruiz, 1938); A. atricaudum Cockerell, 1926; A. aymara Toro & Rodríguez, 1998; A. chilense Spinola, 1851; A. chubuti Cockerell, 1910; A. colliguayanum Toro & Rojas, 1970; A. cuzcoense Schrottky, 1910; A. danieli Urban, 2001; A. decaspilum Moure, 1957; A. deceptum Smith, 1879; A. edwini Ruiz, 1935; A. espinosai Ruiz, 1938; A. falsificum Moure, 1957; A. friesei Cockerell, 1911; A. funereum Schletterer, 1890; A. garleppi Schrottky, 1910 = A. matucanense Cockerell, 1914 syn. nov.; A. gayi Spinola, 1851; A. igori Urban, 2001; A. larocai Urban, 1997; A. latum Schrottky, 1902; A. luizae Urban, 2001; A. manicatum (Linnaeus, 1758); A. masunariae Urban, 2001; A. nigerrimum Schrottky, 1910; A. paitense Cockerell, 1926; A. penai Moure, 1957; A. peruvianum Schrottky, 1910; A. rafaeli Urban, 2001; A. rozeni Urban, 2001; A. rubripes Friese, 1908 = A. boliviense Friese, 1920 syn. nov. = A. adriani Ruiz, 1935 syn. nov. = A. kuscheli Moure, 1957 syn. nov.; A. sanguinicaudum Schwarz, 1933; A. sertanicola Moure & Urban, 1964; A. tarsoi Urban, 2001; A. toro Urban. 2001; A. vigintiduopunctatum Friese, 1904; A. vigintipunctatum Friese, 1908, and A. weyrauchi Schwarz, 1943. Some taxonomic comments are made for each species, and new data on geographic distribution are also given. The females of A. andinum, A. igori, A. rozeni and the male of A. anurospilum are described for the first time. Identification keys (for males and females), as well as illustrations for almost all species, are provided.

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This paper integrates in a unified and tractable framework some of the key insights of the field of international trade and economic growth. It examines a sequence of theoretical models that share a common description of technology and preferences but differ on their assumptions about trade frictions. By comparing the predictions of these models against each other, it is possible to identify a variety of channels through which trade affects the evolution of world income and its geographical distribution. By comparing the predictions of these models against the data, it is also possible to construct coherent explanations of income differences and long-run trends in economic growth.

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The female of Thyrsopelma itaunense (d'Andretta & González, 1964) is described and illustrated for the first time. T. itaunense and T. orbitale are morphologically compared. New records on geographical distribution are aslo presented.

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The genus Loboederus Guérin-Méneville, 1831 formerly included three species: L. appendiculatus (Perty, 1830), L. fleutiauxi Lesne, 1940 and L. luederwaldti Costa-Andrade, 1935. L. fleutiauxi is considered as a junior synonym of L. luederwaldti. The generic characterization and the morphological analysis and redescriptions of both species are presented. The lectotype and paralectotypes of L. luederwaldti are designated and the geographical distribution of both species is widened.

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Mycetarotes is a small genus of the exclusively Neotropical fungus-growing ants, that includes M. parallelus (Emery), M. senticosus Kempf, M. acutus Mayhé-Nunes and M. carinatus Mayhé-Nunes. We hereby revise historical and recent information regarding Mycetarotes species for the first time, providing an identification key to workers, diagnoses, synoptic illustrated redescriptions of the species, including those of sexuals when known, updates of distributional records, and nest pictures of M. carinatus and M. parallelus. We comment the taxonomy and phylogenetic relationships among Mycetarotes and related genera, and on their geographical distribution. The available biological information on the genus is summarized.

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Both sexes of a new phlebotomine sandfly species Micropygomyia (Sauromyia) vonatzingeni sp. nov. (Diptera, Psychodidae), captured in the Serra das Andorinhas, São Geraldo do Araguaia municipality, Pará state, and Cavalcante municipality, Tocantins state, Brazil, are described and illustrated. This new species belongs to the oswaldoi series and its distinction from the other extant species of the series was made by male and female identification keys. The specific geographical distribution of the oswaldoi series by country and department (or state) is presented.

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Three species of Bledius Leach, 1819 are recognized from southern Brazil. A new species is described, B. hermani n. sp., from Paraná and Rio Grande do Sul States and B. fernandezi Bernhauer, 1939 is redescribed. The geographical distribution of B. bonariensis Bernhauer, 1912 and B. fernandezi are extended. A key to identification of Bledius from southern Brazil is also provided.

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The fungus-farming ant genus Mycetagroicus Brandão & Mayhé-Nunes was proposed based on three species from the Brazilian "Cerrado": M. cerradensis, M. triangularis and M. urbanus. Here we describe a new species of Attini ant of the genus Mycetagroicus, M. inflatus n. sp., based on two workers collected in eastern Pará State, Brazil. A new key for species identification, comments on differences among species and new geographical distribution data are furnished.