981 resultados para length at sexual maturity
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Physalaemus henselii (Peters, 1872) is a little known leiuperid frog that has not been studied since the 1960s. Herein, we redescribe its advertisement call, and assess the female sexual cycle and the reproductive period on the basis of the macroscopic analysis of the ovaries and field observations. The Ovarian Size Factor (OSF) was calculated. The study was made in Departamento de Rivera, northern Uruguay. The advertisement call consists of short (177 ± 21ms), multipulsed (20 ± 3 pulses/note) notes, with a note repetition rate of 1.57 ± 0.13 notes/s. Physalaemus henselii has a female sexual cycle with unimodal distribution of gravid females, which are present from February to September. The OSF and the ratio "females with mature oocytes / females without mature oocytes" reached the highest values from April to June. The number and size of oocytes were positively correlated with female size. The smallest female (SVL =18.94mm, weight =0.78g) with mature oocytes was found in July. The observed sexual cycle with a single annual reproductive period during the cold season (autumn and early winter), is an uncommon fact for anuran species in the region.
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The aim of this study was to characterize, for the central region of the State of Rio Grande do Sul, Brazil, the reproductive biology of Leptodactylus fuscus (Schneider, 1799), based on the analysis of gonadal development of males and females, reproductive effort, size-fecundity relationships, and occurrence of sexual dimorphism in body size. Mature individuals were found from October 1996 to February 1997 and from October 1997 to December 1997. The highest input of juveniles in the population was recorded in March 1997. There was a positive and significant correlation between the number of mature individuals and the mean monthly temperature. The population did not present sexual dimorphism in size. Males presented significant correlation only between snout-vent length and testes length. All females had oocytes at four different maturation stages and there were no significant correlations regarding size-fecundity variables. The correlation between ovarian size factor and females snout-vent length was not significant either. The main difference between this population and those that inhabit tropical climate was that temperature was responsible for stimulating the reproduction activity, instead of rainfall.
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O presente estudo tem como objetivo analisar a distribuição de classes de tamanho e proporção sexual ampliando o conhecimento do comportamento reprodutivo de Diplodon expansus (Küster, 1856) e da biodiversidade dos corpos de água da Área de Proteção Ambiental do Piraquara, Paraná, Brasil. A área de estudo corresponde a um trecho do rio Piraquara de águas lóticas, e mata ciliar relativamente bem preservada. Foram realizadas quatro coletas no período de março de 2006 a dezembro de 2006. No rio Piraquara o D. expansus ocorre em substratos arenoso e lodoso. O comprimento dos exemplares variou entre 17 mm e 65 mm, sendo que a maior frequência de classes de comprimento foi registrada para as classes intermediárias. A análise histológica das gônadas possibilitou a determinação de uma razão sexual 1:1, não tendo sido identificado nenhum exemplar hermafrodita, caracterizando uma população tipicamente dióica. Análises qualitativas e quantitativas demonstram uma gametogênese contínua, com picos de liberação larval no verão.
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This study presents original data on the reproduction and feeding ecology of two syntopic amphisbaenians, Amphisbaena munoai Klappenbach, 1969 and Anops kingi Bell, 1833, from southern Brazil. Sampling was carried out from April 2004 to April 2006 at a highland area located in São Jerônimo and Barão do Triunfo municipalities, Rio Grande do Sul, Brazil. A total of 647 amphisbaenians were collected, 510 specimens of A. munoai and 137 specimens of A. kingi, of which 130 and 93, respectively, had their gonads and gut content analyzed. Both species presented a unimodal pattern of seasonal distribution, sexually mature females with significantly larger snout vent length (SVL) than sexually mature males, and seasonal reproductive cycle. Adults of A. kingi had significantly larger (SVL) than those of Amphisbaena munoai. Both species had generalist diets, but termites (Isoptera) was a staple item in their diet. Greater predominance of insect larvae was observed in the diet of A. kingi, which may be due to its larger body in comparison to A. munoai. Insect larvae ingested by A. kingi were significantly larger than those ingested by A. munoai. Diets of adult males and females of both species were not significantly different. The ontogenetic diet comparison in both species revealed significant numerical differences, with adults consuming higher numbers of prey.
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O tamanho da primeira maturação sexual (TPM) em Aegla platensis Schmitt, 1942 foi estimado através das mudanças nas proporções de dimensões corporais dos animais. Para isso, foram realizadas coletas mensais, de julho de 2007 a junho de 2008 no Lajeado Bonito (27º25'27''S, 53º24'39''W), um tributário de primeira ordem do Rio da Várzea, município de Frederico Westphalen, Rio Grande do Sul. Foram utilizados 437 machos com comprimento de cefalotórax (CC) variando de 6,00 mm a 31,75 mm e 368 fêmeas, com tamanhos entre 6,08 mm e 27,92 mm de CC. As seguintes dimensões corporais foram mensuradas em todos os indivíduos coletados: comprimento do cefalotórax (CC), largura do abdome (LA), comprimento do própodo do quelípodo direito (CPD) e comprimento do própodo do quelípodo esquerdo (CPE). Após o registro dessas medidas, os animais foram devolvidos ao mesmo local de captura. As análises de maturidade sexual morfológica foram realizadas com auxílio do software Mature 2, nas quais foram utilizadas as medidas de CC, considerada como variável independente e relacionada com as demais dimensões. As relações que melhor se ajustaram para estas análises, em machos, foram CPD x CC (TPM: CC=18,2 mm) e CPE x CC (TPM: CC=20,1 mm) e LA x CC (TPM: CC=16,5 mm) nas fêmeas.
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Este estudo foi desenvolvido com o objetivo de determinar o tamanho da maturidade morfológica e fisiológica de machos e fêmeas em duas populações de Ucides cordatus (Linnaeus, 1763) de Tamandaré, Pernambuco, Brasil. Os caranguejos foram coletados mensalmente (abril/2008 a março/2009) nos manguezais dos rios Ariquindá e Mamucabas, por um catador, através da técnica de braceamento, durante a maré baixa em três áreas distintas de 25 m² cada. Os caranguejos capturados foram separados por sexo e medidos (largura da carapaça, comprimento do própodo do quelípodo dos machos e largura do 5º somito abdominal das fêmeas). Além disso, os caranguejos foram caracterizados em relação ao estágio de desenvolvimento gonadal. Os caranguejos com gônadas imaturas e rudimentares foram considerados jovens, enquanto os demais foram classificados como adultos (gônada em desenvolvimento, desenvolvida, avançada ou esgotada). O tamanho da largura da carapaça no qual 50% da população de U. cordatus foi considerada madura morfologicamente foi de 38,0 mm (machos) e 35,4 mm (fêmeas) em Ariquindá, enquanto para Mamucabas estes valores foram de 37,3 e 32,9 mm, respectivamente. Na determinação da maturidade sexual fisiológica, os machos e fêmeas de Ariquindá foram considerados maduros com 38,5 e 37,8 mm, respectivamente, enquanto em Mamucabas os tamanhos obtidos foram de 36,2 e 35,8 mm. A maturidade morfológica dos machos ocorreu com tamanho superior ao das fêmeas, provavelmente devido ao seu maior investimento em crescimento somático, enquanto as fêmeas investem mais no processo reprodutivo. Os caranguejos provenientes do manguezal de Mamucabas atingiram a maturidade sexual com tamanhos inferiores aos de Ariquindá, provavelmente devido ao maior impacto verificado para este manguezal.
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The morphological characteristics of the mandible of adult Chaetophractus vellerosus (Gray, 1865) and Zaedyus pichiy (Desmarest, 1804) were studied to establish its generalized design and to identify inter- and intra- (sexual) specific differences. Morphological descriptions were complemented with the application of univariate and multivariate (analysis of correlation matrices, PCA, discriminant analysis) techniques. The mandible of both species is very similar, and is characterized by elevated condyle, well developed angular process, distinct coronoid process, tooth row which extends to the rear end of the angle between body and ramus, and unfused but firm symphysis. Although both armadillos are omnivorous, a more slender configuration of the jaw in Z. pichiy could be indicative of a better adaptation of its masticatory apparatus to insectivory. The PCA showed an almost total segregation of both species on PC1 (47.7% of the total variance), with C. vellerosus being associated to mandibles taller and with wider body and ramus. Zaedyus pichiy was characterized by heavy loadings of length parameters on PC2 (22.6% of the variance). A small degree of sexual dimorphism was found, with size-based differences in C. vellerosus (larger mandibles in females) and shape-based differences in Z. pichiy (taller mandibles in males, longer ones in females). Correlations between variables were higher in males of both species, indicating a more stable shape of the mandible than in females. The selected parameters to discriminate sexes were the body length of the mandible in C. vellerosus (correct classification: ca. 86% in males, 81% in females), and the height of the mandible at the level of the last tooth in Z. pichiy (near 85% of right assignment in both sexes). The inclusion of a new variable (body length) in the latter species improved the classification of the females to 100%. Teeth are typically 10 in C. vellerosus and 9 in Z. pichiy, but aberrancies in this basic number, such as unilateral or bilateral extra or fewer teeth, are common.
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Amphisbaena nigricauda Gans, 1966 is a small, poorly known amphisbaenid endemic to the restinga of the states of Espírito Santo and Bahia, Brazil. We analyze 178 specimens collected in Vitória municipality, state of Espírito Santo, Brazil, to investigate whether this species show sexual dimorphism in pre-cloacal pores and in morphological characters. Sex was determined by a ventral incision and direct inspection of gonads. A PCA analysis was performed to generate a general body size measurement. A T test and the non-parametric Mann-Whitney test were used to assess whether this species show sexual dimorphism on five morphometric and five meristic characters, respectively. Sex could not be determined in 36 specimens because they were mutilated in the posterior portion of their bodies. The diagnosis of the species is redefined based on this sample size: the smallest number of body annuli changes from 222 to 192, the number of dorsal and ventral segments in an annulus in the middle of the body changes to 9-11/13-16 (instead of 10/16), and the autotomic tail annulus lies between annulus 7-10 (instead of 6-9). The number of tail annuli remained within the known range of variation of the species (19-24). None of the 80 females analyzed showed pre-cloacal pores, whereas within males 59 out of 62 specimens displayed four and two specimens displayed five pre-cloacal pores. A single male did not possess pre-cloacal pores, but showed irregular scales on its cloacal region. Sex-based difference based on presence or absence of pre-cloacal pores as well as males with wider head was seen in other Neotropical amphisbaenids. However, a pattern of body size differences between males and females has not been identified so far in the few amphisbaenid species studied in this regard. Further studies on this taxonomic group are still needed to elucidate the existence of general patterns of sexual dimorphism and to identify the selective pressures driving these patterns.
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The filling length of an edge-circuit η in the Cayley 2-complex of a finite presentation of a group is the minimal integer length L such that there is a combinatorial null-homotopy of η down to a base point through loops of length at most L. We introduce similar notions in which the full-homotopy is not required to fix a base point, and in which the contracting loop is allowed to bifurcate. We exhibit a group in which the resulting filling invariants exhibit dramatically different behaviour to the standard notion of filling length. We also define the corresponding filling invariants for Riemannian manifolds and translate our results to this setting.
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Em continuação as pesquisas que vimos realizando nos Embiídeos é feito um estudo comparado das peças bucais entre machos e fêmeas de Embolyntha batesi. A cabeça é prognata recoberta por diminutas cerdas. É a região mais resistente do inseto, devido proteger, além de outros órgãos, principalmente, o sistema nervoso. Varia de tamanho nos dois sexos com os índices (comprimento : largura) na fêmea de 1,06 e nos machos de 1,36; a cabeça da fêmea é achatada, enquanto que a dos machos é alongada. Quase tôdas as suturas são visíveis nos sexos, com excessão de algumas, como é o caso da coronal e post-frontal dos machos. De tôdas as suturas, a temporal é a mais interessante, limita a região do vertex com as genas, ao mesmo tempo que origina um sulco profundo, que penetra na cápsula craniana fazendo parte do esqueleto interno da cabeça, e sendo responsável pelo aspecto diferente das mesmas. A sutura temporal, na região ventral, separa as genas das subgenas. A sutura hipostomal, em ambos os sexos, é muito acentuada, e na sua parte mais interna, vêm se inserir os ramos posteriores do tentório, e, ainda lateralmente, as maxilas. O tentório é primitivo, tendo um corpo central, de forma quadrangular e, de cada ângulo parte um ramo; dois anteriores, menores, que se dirigem para a região dorsal onde se bifurcam, indo ter próximo á base das antenas e mandíbulas, e dois ramos posteriores que seguem a direção ventral, indo ter á região hipostomal. As antenas são filiformes, variando o número de segmentos. Os olhos dos machos são reniformes, salientes e grandes, enquanto que os das fêmeas são pequenos, ovais e achatados. O número de omatídeos de macho é 34, e, na fêmea é 41, em uma determinada área. O clípeo quase não se diferencia da fronte, porém encontra-se dividido em anti-clípeo e post-clípeo. A sutura do clípeo-labro é bem acentuada, deixando transparecer, após a diafanização do material, um espessamento da cutícula na sua região mais interna, destinada a implantação dos músculos que movimentam o labro. Na parte ventral o labro apresenta sensilas, que variam quanto a forma, tamanho e estrutura nos dois sexos. As mandíbulas apresentam-se muito diferentes devida sua função, isto é, trituradora nas fêmeas e preensora nos machos. Pela simples morfologia das mandíbulas podemos identificar o sexo nos Embiídeos. Em ambos temos dentes incisivos e molares, porém mais acentuados nas fêmeas. Nos machos a região interna da mandíbula tem a forma côncava, com cutícula...
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Background and Aims The males and females of many dioecious plant species differ from one another in important life-history traits, such as their size. If male and female reproductive functions draw on different resources, for example, one should expect males and females to display different allocation strategies as they grow. Importantly, these strategies may differ not only between the two sexes, but also between plants of different age and therefore size. Results are presented from an experiment that asks whether males and females of Mercurialis annua, an annual plant with indeterminate growth, differ over time in their allocation of two potentially limiting resources (carbon and nitrogen) to vegetative (below-and above-ground) and reproductive tissues.Methods Comparisons were made of the temporal patterns of biomass allocation to shoots, roots and reproduction and the nitrogen content in the leaves between the sexes of M. annua by harvesting plants of each sex after growth over different periods of time.Key Results and Conclusions Males and females differed in their temporal patterns of allocation. Males allocated more to reproduction than females at early stages, but this trend was reversed at later stages. Importantly, males allocated proportionally more of their biomass towards roots at later stages, but the roots of females were larger in absolute terms. The study points to the important role played by both the timing of resource deployment and the relative versus absolute sizes of the sinks and sources in sexual dimorphism of an annual plant.
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OBJECTIVES: In this population-based study, reference values were generated for renal length, and the heritability and factors associated with kidney length were assessed. METHODS: Anthropometric parameters and renal ultrasound measurements were assessed in randomly selected nuclear families of European ancestry (Switzerland). The adjusted narrow sense heritability of kidney size parameters was estimated by maximum likelihood assuming multivariate normality after power transformation. Gender-specific reference centiles were generated for renal length according to body height in the subset of non-diabetic non-obese participants with normal renal function. RESULTS: We included 374 men and 419 women (mean ± SD, age 47 ± 18 and 48 ± 17 years, BMI 26.2 ± 4 and 24.5 ± 5 kg/m(2), respectively) from 205 families. Renal length was 11.4 ± 0.8 cm in men and 10.7 ± 0.8 cm in women; there was no difference between right and left renal length. Body height, weight and estimated glomerular filtration rate (eGFR) were positively associated with renal length, kidney function negatively, age quadratically, whereas gender and hypertension were not. The adjusted heritability estimates of renal length and volume were 47.3 ± 8.5 % and 45.5 ± 8.8 %, respectively (P < 0.001). CONCLUSION: The significant heritability of renal length and volume highlights the familial aggregation of this trait, independently of age and body size. Population-based references for renal length provide a useful guide for clinicians. KEY POINTS: • Renal length and volume are heritable traits, independent of age and size. • Based on a European population, gender-specific reference values/percentiles are provided for renal length. • Renal length correlates positively with body length and weight. • There was no difference between right and left renal lengths in this study. • This negates general teaching that the left kidney is larger and longer.
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"Vegeu el resum a l'inici del document del fitxer adjunt."
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Polyhydroxyalkanoate (PHA) is a family of polymers composed primarily of R-3-hydroxyalkanoic acids. These polymers have properties of biodegradable thermoplastics and elastomers. Medium-chain-length PHAs (MCL-PHAs) are synthesized in bacteria by using intermediates of the beta-oxidation of alkanoic acids. To assess the feasibility of producing MCL-PHAs in plants, Arabidopsis thaliana was transformed with the PhaC1 synthase from Pseudomonas aeruginosa modified for peroxisome targeting by addition of the carboxyl 34 amino acids from the Brassica napus isocitrate lyase. Immunocytochemistry demonstrated that the modified PHA synthase was appropriately targeted to leaf-type peroxisomes in light-grown plants and glyoxysomes in dark-grown plants. Plants expressing the PHA synthase accumulated electron-lucent inclusions in the glyoxysomes and leaf-type peroxisomes, as well as in the vacuole. These inclusions were similar to bacterial PHA inclusions. Analysis of plant extracts by GC and mass spectrometry demonstrated the presence of MCL-PHA in transgenic plants to approximately 4 mg per g of dry weight. The plant PHA contained saturated and unsaturated 3-hydroxyalkanoic acids ranging from six to 16 carbons with 41% of the monomers being 3-hydroxyoctanoic acid and 3-hydroxyoctenoic acid. These results indicate that the beta-oxidation of plant fatty acids can generate a broad range of R-3-hydroxyacyl-CoA intermediates that can be used to synthesize MCL-PHAs.
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Environmental shifts and life-history changes may result in formerly adaptive traits becoming non-functional or maladaptive. In the absence of pleiotropy and other constraints, such traits may decay as a consequence of neutral mutation accumulation or selective processes, highlighting the importance of natural selection for adaptations. A suite of traits are expected to lose their adaptive function in asexual organisms derived from sexual ancestors, and the many independent transitions to asexuality allow for comparative studies of parallel trait maintenance versus decay. In addition, because certain traits, notably male-specific traits, are usually not exposed to selection under asexuality, their decay would have to occur as a consequence of drift. Selective processes could drive the decay of traits associated with costs, which may be the case for the majority of sexual traits expressed in females. We review the fate of male and female sexual traits in 93 animal lineages characterized by asexual reproduction, covering a broad taxon range including molluscs, arachnids, diplopods, crustaceans and eleven different hexapod orders. Many asexual lineages are still able occasionally to produce males. These asexually produced males are often largely or even fully functional, revealing that major developmental pathways can remain quiescent and functional over extended time periods. By contrast, for asexual females, there is a parallel and rapid decay of sexual traits, especially of traits related to mate attraction and location, as expected given the considerable costs often associated with the expression of these traits. The level of decay of female sexual traits, in addition to asexual females being unable to fertilize their eggs, would severely impede reversals to sexual reproduction, even in recently derived asexual lineages. More generally, the parallel maintenance versus decay of different trait types across diverse asexual lineages suggests that neutral traits display little or no decay even after extended periods under relaxed selection, while extensive decay for selected traits occurs extremely quickly. These patterns also highlight that adaptations can fix rapidly in natural populations of asexual organisms, in spite of their mode of reproduction.