51 resultados para COURTSHIP

em Repositório Institucional UNESP - Universidade Estadual Paulista "Julio de Mesquita Filho"


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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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Mesoclemmys vanderhaegei is a Neotropical chelid lacking basic natural history studies. Based on a film made in December 2004, we describe the courtship behavior in this species. Field observations were conducted at Chapada dos Guimarães, Mato Grosso State, southwestern Brazil, in an oligotrophic stream amidst the savannah like Cerrado formation. We provide a schematic drawing of the behavioral sequences during courtship, as well as a flow diagram describing sequential responses of the female to the male behavioral patterns. Mesoclemmys vanderhaegei courtship behavior is similar to that described for other freshwater chelonians.

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O objetivo deste trabalho foi testar se grupos monossexuais de machos gastam mais energia e exibem perfil agonístico diferente de grupos formados por um macho e uma fêmea na tilápia-do-Nilo (Oreochromis niloticus). Tais diferenças são esperadas, pois machos e fêmeas competem por diferentes recursos reprodutivos. Foram utilizadas duplas de machos (MM) e duplas de macho-fêmea (MF) que permaneceram pareadas por 40 minutos. Durante esse período foi feito o registro da interação agonística (10 minutos iniciais e 10 minutos finais do pareamento) e determinado o gasto energético (consumo de O2) pelo Método de Winckler. A latência para o início dos confrontos (média ± DP, MM = 27,40 ± 25,15 s; MF = 14,22 ± 21,19 s; Mann-Whitney, U = 33,50, P = 0,21) e a freqüência de todas as unidades comportamentais (média ± DP, MM < 72,30 ± 25,29; MF < 73,50 ± 21,65.10/min; Mann-Whitney, P > 0,10) foram semelhantes entre os grupos MM e MF nos 10 minutos iniciais. Isso indica que cada intruso foi considerado um potencial competidor no início da interação. No entanto, a freqüência de ondulação (interação também exibida durante a corte) foi maior para o residente do grupo MF nos 10 minutos finais (média ± DP, MM = 3,56 ± 5,89; MF = 8,56 ± 4,00.10/min; Mann-Whitney, U = 15,50, P = 0,01). A freqüência de fuga, entretanto, foi menor para o intruso do mesmo grupo (média ± DP, MM = 3,90 ± 4,33; MF = 0,44 ± 0,96.10/min; Mann-Whitney, U = 23,50, P = 0,04). Além disso, o perfil agonístico no grupo MM foi composto por um maior número de itens comportamentais do que o MF (para residentes e intrusos). Apesar das diferenças comportamentais, o consumo de O2 não foi afetado pela composição sexual do grupo (média ± DP, MM = 1,93 ± 0,54; MF = 1,77 ± 0,46 mgO2.g peso seco-1.40/min; t-teste de Student, t = 0,71, P = 0,49).

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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Este experimento foi realizado para avaliar o efeito do farelo e da farinha de algodão no comportamento reprodutivo e na atividade testicular de reprodutores de tilápia do Nilo. Vinte e cinco peixes receberam dietas contendo 0; 2; 4; e 6% de semente de algodão descorticada e moída e 24,0% de farelo de algodão. O comportamento reprodutivo foi observado e a construção de ninhos, corte e desova, avaliadas. Aos 90 dias, as gônadas dos machos foram avaliadas microscopicamente. O grupo controle (farelo de algodão) obteve maior número de desovas. Os peixes alimentados com semente ou farelo de algodão, apesar de não terem apresentado o mesmo número de desovas, construíram ninhos e fizeram a corte. A análise histológica dos testículos demonstrou que a adição de 24,0% de farelo ou níveis de 2,0% ou superiores da farinha influiu na atividade testicular. O gossipol presente na farinha ou farelo de algodão teve efeito negativa nas gônadas destes animais.

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The relative growth of the xanthid crab, Panopeus austrobesus was investigated by means of the allometric method. Crabs were obtained in the mangrove formed by the estuary of the rivers Comprido and Escuro (23degrees29'24S 45degrees10'12W), Ubatuba, São Paulo State, Brazil. All crabs were measured to obtain their carapace width (CW) and length (CL), abdomen width (AW) at the basis of the 5(th) somite, and major cheliped propodus length (PL) and height (PH). Males were also measured for their gonopod length (GL). The size of crabs based on CW ranged from 4.0 to 44.8 mm for males and 3.1 to 34.5 mm for females. The relative growth equation (Y = aX(b)) based on the relationship between GL and CW suggested that males reach their sexual maturity near 14.6 mm CW. Such relationship shows a positive allometry during the juvenile phase and an isometric growth in adult life. In females, the estimated size at 50% maturity is 13.0 mm CW, based on the relationship AW vs. CW. Males reach larger sizes than females, which probably provides them better conditions to protect females during courtship. Concerning cheliped size, approximately 73% of the crabs analysed (N = 209), disregarding sex, have the right PL larger than the left. The PL growth shows that specimens with a left major cheliped (26%) have a higher allometric coefficient, despite being smaller considering their CW. Such a difference may compensate the smaller size of the crab during defense or prey capture.

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In this study, the reproductive behavior exhibited by Arenaeus cribrarius in captivity was described, and the duration of each behavioral stage was measured. Swimming crabs were trawled in Ubatuba, northern littoral of São Paulo State, Brazil, and maintained in aquaria. Water conditions and food items were provided according to this species' natural requirements in the wild. In the presence of premolt females, intermolt males exhibited a courtship display that became intensified when the potential mate was visually perceived. After mate selection, the male carried the female under itself (precopulatory position) for 29.8 +/- 5.1 d until the female molted. Afterwards, the male manipulated the recently molted female, and inverted her position under itself as to penetrate her with his first pair of pleopods (copulation), a process that took 17.1 +/- 4.6 h. After copulation the male continued to carry his soft-shelled mate for 29.7 +/- 5.8 d (postcopulatory position). The time elapsed between copulation and spawning was 57.8 +/- 3.8 d and the time interval between successive spawns 33.8 +/- 7.1 d. Total embryonic development took 13.5 +/- 2.1 d in temperature conditions of 25.0 +/- 2.0 degrees C. During the last 4.7 +/- 1.4 d embryos' eyes were already visible. The reproductive behavior pattern in A. cribrarius is very similar to those previously described in other portunids.

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A morphometric study of the xanthoid crab Hexapanopeus schmitti was carried out, using the allometric method. Samples were taken monthly for two years (1998-1999) in the Ubatuba region, northern coast of São Paulo, Brazil. Sex and size were assessed for each specimen, and all crabs were measured to obtain their carapace width (CW) and length (CL), abdomen width (AW) of females, major cheliped propodus length and height (PL and PH), and gonopod length (GL) of males. A total of 301 crabs were analyzed, 209 males and 92 females. The CWs of the crabs ranged from 2.5 to 9.8 mm for males and from 2.8 to 9.4 mm for females. The relative growth equation (y=ax(b)) based on the relationship between GL and CW suggested that males reach their morphological sexual maturity near 6.1 mm CW. In females, the estimated size at 50 % maturity was 4.8 mm CW, based on the relationship of AW vs. CW. Males reach larger sizes than females, which probably favors their ability to guard the females during courtship. In approximately 83 % of the crabs (n= 371), disregarding sex, the right cheliped was larger.

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This article presents preliminary information about the reproduction of two species of freshwater stingrays of the genus Potamotrygon, found in the Upper Parana River (Southwest Brazil), where these animals are exotic. Males of P. motoro and P. falkneri become sexually mature around 270 mm and 260 mm of disc width (DW), respectively. Females become sexually mature around 330 mm of DW in P. motoro and 325 mm in P. falkneri. In both species, females are bigger and heavier than males, reaching about 700 mm of DW and 20 kg. Copulating has not been recorded, but one courtship ritual has been observed during the dry season. Mature males present a different dentition from females and young males, which is probably related to their reproductive behavior instead of to their feeding habit. The female fertility has varied from one to three offspring. A miscarriage has been observed at different stages of embryonic development always when pregnant females were captured. In spite of the great history of anthropization of the study area, it seems that hydrological cycles are related to the reproduction of stingrays. Nevertheless, it would be necessary to conduct deeper studies to verify or not this influence.

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Descrevemos o comportamento reprodutivo de Adelosgryllus rubricephalus Mesa & Zefa, 2004. em observações realizadas em laboratório verificamos a seguinte seqüência no comportamento de acasalamento: (1) reconhecimento sexual por antenação; (2) corte, em que o macho volta seu abdômen em direção à fêmea, vibra as antenas médio-lateralmente, treme o corpo ântero-posteriormente e estridula intermitentemente, enquanto a fêmea receptiva toca a ponta do abdômen, os cercos e os fêmures posteriores do macho, com seus palpos ou tarsos anteriores; o macho então fica imóvel por alguns segundos, expõe o espermatóforo e ambos retomam a seqüência comportamental descrita acima; (3) cópula: o macho coloca-se sob a fêmea, com suas tégminas inclinadas para frente, anexa sua genitália à dela e promove a transferência do esperma; a fêmea desce de cima do macho e ocorre brevemente a posição end-to-end durante a separação do casal; (4) pós-cópula: não há comportamento de guarda; o macho retém o espermatóforo e o ingere. Quantificamos o intervalo de tempo das principais etapas do acasalamento e discutimos suas possíveis implicações no comportamento observado.

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Males of the South American treefrog Aplastodiscus perviridis construct concealed subterranean nests. Using a complex courtship behavior that involves tactile stimuli and vocalizations, males guide the females to the subterranean nests where eggs are laid. Embryos and facultatively oophagous tadpoles (at least in stage 25) stay in subterranean nests until flooding transports them to ponds or streams. This is a rare reproductive mode previously known for few species in the Hyla albosignata and H. albofrenata complexes. Based on similarities of reproductive mode we suggest a monophyletic origin for Aplastodiscus and these complexes of Hyla.

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Social behavior of Hypsiboas albomarginatus was studied in the Atlantic rain forest, Municipality of Ubatuba, in the north coast of the State of São Paulo, southeastern Brazil. Vocalizations of H. albomarginatus are described, including contexts in which they were emitted and temporal and spectral parameters differentiating advertisement from aggressive calls. Dominant call frequency was inversely correlated with male length and body mass but not with environmental temperature. Number of pulses per note was not correlated with any variable, and advertisement call amplitude was influenced by temperature and time. During chorus aggregation, males interacted acoustically by emitting advertisement calls in antiphony, or by emitting aggressive calls. Some disputes among males culminated in physical combat; males performed kicks and slaps on rivals' heads, in an apparent attempt to dislodge rivals from perches. Visual signals were also displayed during conflicts between males, contributing to an escalation of aggressive behavior. Visual signals were not recorded during courtship between males and females but may help in the accurate localization of the signaling male during aggressive interactions.

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The present study was conducted in the Serra do Japi in the State of São Paulo, Brazil. From March 2004 to January 2006 we studied the ecology and reproductive biology of two sympatric species of Aplastodiscus in three different habitats: lake, stream, and swamp. The majority of A. leucopygius males in calling activity were recorded during the rainy season and during sporadic rains in the dry season (April to September). The same was observed for A. arildae. Most courtship displays of A. leucopygius were observed mainly during the rainy period and only one courtship behaviour was observed for A. arildae during a rainy night, in December 2005. Aplastodiscus leucopygius males were found in activity in the three habitats surveyed. In contrast, males of A. arildae were found in only one habitat (stream). Spatial distribution seems to be the main mechanism of reproductive segregation between the studied species.