988 resultados para Ranade, Mahadev Rao Bahadur, 1842-1901.
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Mode of access: Internet.
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Introduction by H. H. Harper.
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Mode of access: Internet.
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Dates d'aprs les activits de Victor Gille au Conservatoire et la mort de Massenet
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f. 3-4 : dat d'aprs le contenu
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f.3-4 : dats d'aprs l'anne de dcs de Franz Servais
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f.1-5, 12-16, 18-26 : lettres, f.6-11 : cartes-lettres, f.17,28-31 : lettres sur papier de deuil ; enveloppe jointe au f.13 ; f.1-2, 12, 15-22 : dats d'aprs le contenu ; f.23-31 : dats d'aprs l'anne de dcs de l'auteur
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It is presented a cladistic analysis of the Dicrepidiina aiming to test the monophyletism of the subtribe and to establish the relationships among the genera. The subtribe is composed by 36 genera and all of them, except Asebis, Lamononia, Neopsephus, Semiotopsis and Spilomorphus were included in the analysis. Fifty two species, especially the type-species of each genus were studied: Achrestus flavocinctus (Candze, 1859), A. venustus Champion, 1895, Adiaphorus gracilis Schwarz, 1901, A. ponticerianus Candze, 1859, Anoplischiopsis bivittatus Champion, 1895, Anoplischius bicarinatus Candze, 1859, A. conicus Candze, 1900, A. haematopus Candze, 1859, A. pyronotus Candze, 1859, Atractosomus flavescens (Germar, 1839), Blauta cribraria (Germar, 1844), Calopsephus apicalis (Schwarz, 1903), Catalamprus angustus (Fleutiaux, 1902), Crepidius flabellifer (Erichson, 1847), C. resectus Candze, 1859, Cyathodera auripilosus Costa, 1968, C. lanugicollis (Candze, 1859), C. longicornis Blanchard, 1843, Dayakus angularis Candze, 1893, Dicrepidius ramicornis (Palisot de Beauvois, 1805), Dipropus brasilianus (Germar, 1824), D. factuellus Candze, 1859, D. laticollis (Eschscholtz, 1829), D. pinguis (Candze, 1859), D. schwarzi (Becker, 1961), Elius birmanicus Candze, 1893, E. dilatatus Candze, 1878, Heterocrepidius gilvellus Candze, 1859, H. ventralis Gurin-Mneville, 1838, Lampropsephus cyaneus (Candze, 1878), Loboederus appendiculatus (Perty, 1830), Olophoeus gibbus Candze, 1859, Ovipalpus pubescens Solier, 1851, Pantolamprus ligneus Candze, 1896, P. mirabilis Candze, 1896, P. perpulcher Westwood, 1842, Paraloboderus glaber Golbach, 1990, Proloboderus crassipes Fleutiaux, 1912, Propsephus beniensis (Candze, 1859), P. cavifrons (Erichson, 1843), Pseudolophoeus guineensis (Candze, 1881), Rhinopsephus apicalis (Schwarz, 1903), Sephilus formosanus Schwarz, 1912, S. frontalis Candze, 1878, Singhalenus gibbus Candze, 1892, S. taprobanicus Candze, 1859, Sphenomerus antennalis Candze, 1859, S. brunneus Candze, 1865, Spilus atractomorphus Candze, 1859, S. nitidus Candze, 1859, Stenocrepidius simonii Fleutiaux, 1891 and Trielasmus varians Blanchard, 1846. Chalcolepidius zonatus (Hemirhipini, Agrypninae), Ctenicera silvatica (Prosternini, Prosterninae), and species of the other subtribes of Ampedini (Elaterinae): Ampedus sanguineus (Ampedina), Melanotus spernendus (Melanotina) and Anchastus digittatus and Physorhinus xanthocephalus (Physorhinina) were used as outgroups. The results of the phylogenetic analysis demonstrated that Dicrepidiina, as formerly defined, does not form a monophyletic group. One genus, represented by Ovipalpus pubescens, was removed from the subtribe. The subtribe is characterized by presence of lamella under 2nd and 3rd tarsomeres of all legs. Also, it was revealed that the genera Achrestus, Anoplischius, Dipropus and Propsephus are not monophyletic. Due to the scarcity of information, all the studied species are redescribed and illustrated.
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Foram estudados os efeitos da adio de plantas medicinais de princpios cicatrizantes (Centelha asitica, Papana e Confrei) na rao controle de caracis terrestres, para se avaliar a interferncia destas plantas na composio do muco glicoprotico. Foram utilizados 80 caracis terrestres Achatina sp, baseados em um peso homogneo (49 e 40 g e idade mdia de 10 e 19 meses para Achatina fulica e Achatina monochromatica, respectivamente). Os animais foram distribudos aleatoriamente em oito grupos experimentais: controle Achatina fulica (FC) e Achatina monochromatica (MC), centelha asitica Achatina fulica (FCe) e Achatina monochromatica (MCe), papana Achatina fulica (FPa) e Achatina monochromatica (MPa) e confrei Achatina fulica (FCo) e Achatina monochromatica (MCo). gua e rao foram fornecidos ad libitum. Ao final de 150 dias de tratamento, os animais foram submetidos tcnica de extrao do muco glicoprotico, por meio do estmulo manual da glndula podal, responsvel pela secreo deste muco. Esta metodologia considerou o bem-estar dos animais, uma vez que os mesmos no foram sacrificados e retornaram ao seu sistema de criao. Os mucos foram analisados por meio de testes colorimtricos e espectroscpicos, que constataram alteraes semelhantes, porm apresentaram variao significativa em sua composio glicoprotica.
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The present study determined the distribution pattern of the hermit crab Loxopagurus loxochelis by a comparison of catch, depth and environmental factors at two separate bays (Caraguatatuba and Ubatuba) of Sao Paulo State, Brazil. The influence of these parameters on the distribution of males, non- ovigerous females and ovigerous females was also evaluated. Crabs were collected monthly, over a period of one year (from July/2002 to June/2003), in seven depths, from 5 to 35 m. Abiotic factors were monitored as follows: superficial and bottom salinity (psu), superficial and bottom temperature (C), organic matter content (%) and sediment composition (%). In total, 366 hermit crabs were sampled in Caraguatatuba and 126 in Ubatuba. The highest frequency of occurrence was verified at 20 m during winter (July) in Caraguatatuba and 25 m during summer (January) in Ubatuba. The highest occurrences were recorded in the regions with bottom salinities ranging from 34 to 36 psu, bottom temperatures from 18 to 24 C and, low percentages of organic matter, gravel and mud; and large proportion of sand in the substrate. There was no significant correlation between the total frequency of organisms and the environmental factors analyzed in both regions. This evidence suggests that other variables as biotic interactions can influence the pattern of distribution of L. loxochelis in the analyzed region, which is considered the limit of the northern distribution of this species.
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We derive the Cramer-Rao Lower Bound (CRLB) for the estimation of initial conditions of noise-embedded orbits produced by general one-dimensional maps. We relate this bound`s asymptotic behavior to the attractor`s Lyapunov number and show numerical examples. These results pave the way for more suitable choices for the chaotic signal generator in some chaotic digital communication systems. (c) 2006 Published by Elsevier Ltd.