66 resultados para HORRIDUS
Resumo:
Os autores fazem um estudo de todas as espécies do gênero Rhopalias Stiles & Hassall, 1898, ratificando quatro espécies e invalidando duas. Ficando assim o gênero com as espécies R. coronatus (Rudolphi, 1819), R. horridus (Diesing, 1850), R. baculifer Braun, 1901 e R. macracanthus Chandler, 1932, as quais são no presente trabalho bem caracterizadas com descrições, quadros comparativos e figuras. Nesta oportunidade aproveitam para determinar todo material pertencente ao gênero depositado na Coleção Helmintológica do Instituto Oswaldo Cruz.
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Specimens of elasmobranch fishes, captured in the states of Paraná and Santa Catarina, of the southern coast off Brazil, represented by three families, four genera, and four species, were parasitized with otobothrioid trypanorhynch cestodes: Heptranchias perlo (Bonnaterre, 1788), Squalus sp. and Carcharhinus signatus (Poey, 1868) were parasitized with Progrillotia dollfusi Carvajal & Rego,1987; Prionace glauca (Linnaeus, 1758) with Molicola horridus (Goodsir, 1841) Dollfus, 1942. Details of internal morphology and/or scolex and/or proglottids surface ultrastructure, that expanded the description of M. horridus, through observations with lightfield, and/or scanning eletronic microscopy, are provided. The known geographical distribution for the species M. horridus is enlarged. P. dollfusi is reported for the first time in elasmobranchs.
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Track analysis of the Neotropical Entimini (Coleoptera, Curculionidae, Entiminae). Distributional patterns of the species belonging to the tribe Entimini from the Neotropical region were analyzed. Based on a track analysis of 22 species of Entimus, Rhigus, and Phaedropus, for which distributional data were available, two generalized tracks were found. One is located in northern Brazil, corresponding to the Amazonian subregion, and is determined by Phaedropus candidus and Rhigus speciosus. The other is located in southern Brazil, corresponding to the Parana subregion, and is determined by Entimus imperialis, E. excelsus, Phaedropus togatus, Rhigus dejeanii, R. faldermanni, R. horridus, R. lateritus, R. nigrosparsus, and R. tribuloides. The development of the Chacoan subregion is hypothesized to have been the dynamic vicariant event that fragmented the former Amazonian-Parana forest.
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Secções de raízes e cladódios de cinco espécies de Cactaceae ocorrentes em uma região de caatinga de Pernambuco (Harrisia adscendens (Gürke) Britton & Rose; Melocactus × horridus Wedermann Notizbl.; M. zenhtneri (Britton & Rose) Luetzelb.; Tacinga inamoena (Schumann) Taylor & Stuppy e T. palmadora (Britton & Rose) Taylor & Stuppy), foram analisadas para verificação de caracteres diagnósticos e adaptativos. As secções foram coradas com safranina e azul de astra e montadas em glicerina. As observações feitas mostraram que a estrutura interna das raízes é bastante similar não sendo observados caracteres diagnósticos. No xilema secundário das raízes ocorrem amplos raios pericíclicos representando um importante caracter adaptativo. O cladódio apresenta os seguintes caracteres diagnósticos e adaptativos: tipos de espinho; tipo e posição dos estômatos; estrutura da hipoderme; tipo e posição das estruturas mucilaginosas; aspecto geral do sistema vascular; ocorrência de feixes corticais e medulares; presença de cristais na epiderme e hipoderme e presença de parênquima aqüífero. Os resultados deste trabalho mostram que as espécies estudadas são cactos típicos apresentando caracteres, que podem ser responsáveis pelo sucesso destas plantas em ambientes adversos como a caatinga.
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Habitat use affects food intake, reproductive fitness and body temperature control in reptiles. Habitat use depends on both the characteristics of the animal and the environmental heterogeneity. In this study we investigated habitat use in a population of the South-American rattlesnake, Crotalus durissus, in a cerrado (the Brazilian savanna) remnant, in south-eastern Brazil. In general, snakes appeared to be thermal generalists. However, they showed substrate temperature preferences in the rainy season, when they selected colder substrates during the day and warmer substrates at night. Individuals were predominantly active on the surface and more frequently found under bushes. Furthermore, in general, the principal component analysis results indicate that rattlesnakes are generalists regarding the microhabitat variables examined in this study. These habitat characteristics, associated with a low thermal selectivity, indicate that rattlesnakes are able to colonize deforested areas where shade occurrence and vegetation cover are similar to those in the cerrado.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Life-history information constitutes the raw data for building population models used in species conservation. We provide life-history data for the endangered Santa Catalina Island Rattlesnake, Crotalus catalinensis. We use data from 277 observations of C. catalinensis made between 2002 and 2011 on the island. Mean snout-vent length (SVL) of adult C. catalinensis was 643 mm for males and 631 mm for females; the difference was not significant. The degree of sexual size dimorphism (SSD; using SVL) was -0.02. However, sexes were dimorphic in total length ( SVL + tail length), relative tail length, and stoutness. Juvenile recruitment occurs during late-summer. In their first year of life, juveniles seem to grow at a rate of about 1.7 cm/mo. Females seem to become mature around 570 mm SVL, probably in the year when they become 2 y old. Scattered literature data corroborates the time of juvenile recruitment described herein. Growth in C. catalinensis seems to be slower than that of C. ruber, its sister taxa, but similar to other rattlesnakes.
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As part of an ongoing revision of the family Gonyleptidac, we have identified many species that are synonyms of previously described species or misplaced in this family. This article summarizes these findings, adding previously unavailable information or correcting imprecise observations to justify the presented taxonomic changes. The following new familial or subfamilial assignments are proposed: Nemastygnus Roewer, 1929 and Taulisa Roewer, 1956 are transferred to Agoristenidae, Agoristeninae; Napostygnus Roewer, 1929 to Cranaidae; Ceropachylinus peruvianus Roewer, 1956 and Pirunipygus Roewer, 1936 are transferred to Gonyleptidae, Ampycinae; Gyndesops Roewer, 1943, Haversia Roewer, 1913 and Oxapampeus Roewer, 1963 are transferred to Gonyleptidae, Pachylinae. The following generic synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes Mello-Leitao, 1922 = Centroleptes Roewer, 1943; Acrographinotus Roewer, 1929 = Unduavius Roewer, 1929; Gonyleptes Kirby, 1819 = Collonychium Bertkau, 1880; Mischonyx Bertkau, 1880 = Eugonyleptes Roewer, 1913 and Gonazula Roewer, 1930; Parampheres Roewer, 1913 = Metapachyloides Roewer, 1917; Pseudopucrolia Roewer, 19 12 = Meteusarcus Roewer, 1913; Haversia Roewer, 19 13 = Hoggellula Roewer, 1930. The following specific synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes singularis (Mello-Leitao, 1935) = Centroleptes flavus Roewer, 1943, syn. n.; Geraeocormobius sylvarum Holmberg, 1887 = Discocyrtus serrifemur Roewer, 1943, syn. n.; Gonyleptellus bimaculatus (Sorensen, 1884) = Gonyleptes cancellatus Roewer, 1917, syn. n.; Gonyleptes atrus Mello-Leitao, 1923 = Weyhia brieni Giltay, 1928, syn. n.; Gonyleptes fragilis Mello-Leitao, 1923 = Gonyleptes banana Kury, 2003, syn. n.; Gonyleptes horridus Kirby, 1819 = Collonychium bicuspidatum Bertkau, 1880, syn. n., Gonyleptes borgmeyeri Mello-Leitao, 1932, syn. n., Gonyleptes curvicornis Mello-Leitao, 1932, syn. n., Metagonyleptes hamatus Roewer, 1913, syn. n. and Paragonyleptes simoni Roewer, 1930, syn. n.; Gonyleptes pustulatus Sorensen, 1884 = Gonyleptes guttatus Roewer, 1917, syn. n.; Haversia defensa (Butler, 1876) = Sadocus vallentini Hogg, 1913, syn. n.; Liogonyleptoides minensis (Piza, 1946) = Currala bahiensis Soares, 1972, syn. n.; Megapachylus grandis Roewer, 1913 = Metapachyloides almeidai Soares & Soares, 1946, syn. n.; Mischonyx cuspidatus (Roewer, 1913) = Gonazula gibbosa Roewer, 1930 syn. n.; Mischonyx scaber (Kirby, 1819) = Xundarava holacantha Mello-Leitao, 1927, syn. n.; Parampheres tibialis Roewer, 1917 = Metapachyloides rugosus Roewer, 1917, syn. n.; Parapachyloides uncinatus (Sorensen, 1879) = Goyazella armata Mello-Leitao, 1931, syn. n.; Pseudopucrolia mutica (Perry, 1833) = Meteusarcus armatus Roewer, 1913, syn. n. The following new combinations are proposed: Acrographinotus ornatus (Roewer, 1929), comb. n. (ex Unduavius); Gonyleptellus bimaculatus (Sorensen, 1884), comb. n. (ex Gonyleptes); Gonyleptes perlatus (Mello-Leitao, 1935), comb. n. (ex Moojenia); Mischonyx scaber (Kirby, 1819), comb. n. (ex Gonyleptes); and Neopachyloides peruvianus (Roewer, 1956), comb. n. (ex Ceropachylus). The following species of Gonyleptidae, Gonyleptinae are revalidated: Gonyleptes atrus Mello-Leitao, 1923 and Gonyleptes curvicornis (Roewer, 1913).
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Well-preserved Mesozoic radiolarian faunas have been recovered at four sites of Deep Sea Drilling Project Leg 62. Late Early Cretaceous assemblages, which occur always with foraminifers or calcareous nannoplankton, allow the description of 21 new species, the introduction of a new zone scheme, and calibration of the radiolarian zones with the geochronological scale.
Resumo:
El prólogo de la tragedia despliega dos espacios distintivos: las silvae de Hipólito y el opresivo y lujurioso espacio interior del palacio de Fedra. Cada personaje es definido por las características de los espacios que sus discursos configuran: los castos y salvajes bosques de Hipólito revelarán, bajo su manto de agreste tranquilidad, una violenta y estéril dicción que sugiere una inadecuación del personaje al paradigma de sapiens que parte de la crítica ha visto en él, mientras que el espacio interior de Fedra estará lleno de llamas y vapor, símbolos de su pasión. Ambos mundos conviven a modo de compartimentos estancos: frío y llamas, castidad y libido, nieve y vapor conviven pacíficamente, y en esta convivencia no hay ni catástrofe ni tragedia. Éstas se desarrollan y toman fuerza a medida que Fedra se adentra discursivamente en los dominios de Hipólito y los tiña progresivamente con su discurso, convirtiéndolo finalmente en un locushorridus donde el joven cazador huirá horrorizado como las bestias que solía perseguir. Por lo tanto tragedia y catástrofe ocurren cuando las silvae de Hipólito se convierten en el acechante Nemus habitado por lujuriosas criaturas gracias a la intrusión discursiva que la reina realiza en el áspero paisaje configurado en la monodia inicial del personaje
Resumo:
El prólogo de la tragedia despliega dos espacios distintivos: las silvae de Hipólito y el opresivo y lujurioso espacio interior del palacio de Fedra. Cada personaje es definido por las características de los espacios que sus discursos configuran: los castos y salvajes bosques de Hipólito revelarán, bajo su manto de agreste tranquilidad, una violenta y estéril dicción que sugiere una inadecuación del personaje al paradigma de sapiens que parte de la crítica ha visto en él, mientras que el espacio interior de Fedra estará lleno de llamas y vapor, símbolos de su pasión. Ambos mundos conviven a modo de compartimentos estancos: frío y llamas, castidad y libido, nieve y vapor conviven pacíficamente, y en esta convivencia no hay ni catástrofe ni tragedia. Éstas se desarrollan y toman fuerza a medida que Fedra se adentra discursivamente en los dominios de Hipólito y los tiña progresivamente con su discurso, convirtiéndolo finalmente en un locushorridus donde el joven cazador huirá horrorizado como las bestias que solía perseguir. Por lo tanto tragedia y catástrofe ocurren cuando las silvae de Hipólito se convierten en el acechante Nemus habitado por lujuriosas criaturas gracias a la intrusión discursiva que la reina realiza en el áspero paisaje configurado en la monodia inicial del personaje
Resumo:
El prólogo de la tragedia despliega dos espacios distintivos: las silvae de Hipólito y el opresivo y lujurioso espacio interior del palacio de Fedra. Cada personaje es definido por las características de los espacios que sus discursos configuran: los castos y salvajes bosques de Hipólito revelarán, bajo su manto de agreste tranquilidad, una violenta y estéril dicción que sugiere una inadecuación del personaje al paradigma de sapiens que parte de la crítica ha visto en él, mientras que el espacio interior de Fedra estará lleno de llamas y vapor, símbolos de su pasión. Ambos mundos conviven a modo de compartimentos estancos: frío y llamas, castidad y libido, nieve y vapor conviven pacíficamente, y en esta convivencia no hay ni catástrofe ni tragedia. Éstas se desarrollan y toman fuerza a medida que Fedra se adentra discursivamente en los dominios de Hipólito y los tiña progresivamente con su discurso, convirtiéndolo finalmente en un locushorridus donde el joven cazador huirá horrorizado como las bestias que solía perseguir. Por lo tanto tragedia y catástrofe ocurren cuando las silvae de Hipólito se convierten en el acechante Nemus habitado por lujuriosas criaturas gracias a la intrusión discursiva que la reina realiza en el áspero paisaje configurado en la monodia inicial del personaje
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This paper documents the biostratigraphic distribution and abundance of diatoms from sites drilled during Ocean Drilling Program Leg 178, off the Pacific margin of the Antarctic Peninsula. Drift sediments cored on the continental rise at Sites 1095, 1096, and 1101 have good recovery and a well-defined paleomagnetic record. Well-preserved diatoms are present throughout the upper Miocene to middle Pliocene and in the upper Quaternary section of these sites. The stratigraphic occurrence of diatom species through these intervals defines numerous datum levels. Diatom events are given absolute age estimates through direct correlation to the established paleomagnetic stratigraphy of Sites 1095, 1096, and 1101. Leg 178 diatom biostratigraphic results enable the development of a regional stratigraphic framework for the Pacific sector of the Southern Ocean and record the interaction of open-ocean and shelf-margin diatom floras.