RESUMO
Gravid female lizards often experience reduced thermal preferences and impaired locomotor performance. These changes have been attributed to the physical burden of the clutch, but some authors have suggested that they may be due to physiological adjustments. We compared the thermal biology and locomotor performance of the lizard Liolaemus wiegmannii 1 week before and 1 week after oviposition. We found that gravid females had a thermal preference 1°C lower than that of non-gravid females. This was accompanied by a change in the thermal dependence of maximum running speed. The thermal optimum for locomotor performance was 2.6°C lower before oviposition than after. At relatively low temperatures (22 and 26°C), running speeds of females before oviposition were up to 31% higher than for females after oviposition. However, at temperatures above 26°C, females achieved similar maximum running speeds (â¼1.5â mâ s-1) regardless of reproductive stage. The magnitude of the changes in thermal parameters and locomotor performance of L. wiegmannii females was independent of relative clutch mass (clutches weighed up to 89% of post-oviposition body mass). This suggests that the changes are not simply due to the clutch mass, but are also due to physiological adjustments. Liolaemus wiegmannii females simultaneously adjusted their own physiology in a short period in order to improve locomotor performance and allocated energy for embryonic development during late gravid stage. Our findings have implications for understanding the mechanisms underlying life histories of lizards on the fast extreme of the slow-fast continuum, where physiological exhaustion could play an important role.
Assuntos
Lagartos , Oviposição , Reprodução , Animais , Lagartos/fisiologia , Feminino , Reprodução/fisiologia , Oviposição/fisiologia , Temperatura , Corrida/fisiologia , Locomoção/fisiologiaRESUMO
Members of Sarcophagidae are necrophagous and are commonly found on decaying carcasses; and their developmental forms are important indicators for the approximation of lowest postmortem interval (PMImin). This work describes the biological characteristics of Sarcophaga argyrostoma from Tehran, Iran. Various temperature regimes were applied to estimate the thermal summation constant (k) and thermal requirements for development of S. argyrostoma. Five growth proceedings, containing 1st ecdysis, 2nd ecdysis, wandering, pupariation and eclosion, were investigated under eight fixed temperature regimes (6-30 °C). The effects of fly age, freshness, and availability of oviposition substrate on oviparity and viviparity was studied. At 6 °C, no development occurs, and at 8 °C only the first ecdysis occurs. At temperatures between 10 and 30 °C, all immature stages proceeded to the adult stage, and thus immature development was analyzed at these six remaining temperatures. The development phases needed minimum (Dz ± SE) 5.4(0.4), 8.5(0.26), 5.3(0.44), 3.8(0.1), and 6.6 (0.6)°C to attain one of the succeeding developmental occasion, correspondingly. The approximated K for those five occasions were 15.04 ± 1.12, 12.62 ± 0.65, 140.36 ± 4.35, 14.59 ± 0.6, and 222.8 ± 4.18°-day (DD) accordingly. When the food substrate is available and fresh, the female prefers to lay eggs, no matter how old she is. However, the chance of ovoviviparity increased when no oviposition substrate was available. The truth that S. argyrostoma able to either larviposit or to lay eggs encompasses serious consequences for the precise estimation of the PMImin, as the existence of larvae resulting from eggs laid on the carcass could add hours (based on ambient temperature) to the PMImin.
RESUMO
Pregnancy is a physiological cost of reproduction for animals that rely on fleeing to avoid predators. Costs of reproduction are predicted to differ between alternative reproductive strategies or modes, such as egg-laying (oviparity) or live-bearing (viviparity). However, disentangling the factors that comprise this cost and how it differs for oviparous or viviparous females is challenging due to myriad environmental, biological, and evolutionary confounds. Here, we tested the hypothesis that costs of pregnancy differ between oviparous and viviparous common lizards (Zootoca vivipara). We predicted that the degree of locomotor impairment during pregnancy and therefore the cost of reproduction would be higher in viviparous females. We conducted our experiment in a hybrid zone containing oviparous and viviparous common lizards. Due to the common environment and inclusion of hybrid individuals, we could infer whether differences were inherent to parity mode. We found that the average and maximum running speed of pregnant females was slower than after they had given birth or laid eggs. Viviparous females experienced an additional pregnancy weight burden and for a longer time period, but were not slower at running than pregnant oviparous females. In addition, we found a parity mode-specific effect of reproductive investment; producing larger clutches was costlier for the locomotor performance of viviparous females for reasons other than the mass increase. Locomotor costs were found to be intermediate in hybrid females, indicating that they are specific to each reproductive mode. Our study shows that viviparous females experience an additional physical and physiological cost of pregnancy and reproductive investment. This two-fold cost implies that viviparous females modulate resource allocation decisions and/or adjust their behavioural responses that result from locomotor impairment.
RESUMO
Evolutionary transitions from egg laying (oviparity) to live birth (viviparity) are common across various taxa. Many species also exhibit genetic variation in egg-laying mode or display an intermediate mode with laid eggs containing embryos at various stages of development. Understanding the mechanistic basis and fitness consequences of such variation remains experimentally challenging. Here, we report highly variable intra-uterine egg retention across 316 Caenorhabditis elegans wild strains, some exhibiting strong retention, followed by internal hatching. We identify multiple evolutionary origins of such phenotypic extremes and pinpoint underlying candidate loci. Behavioral analysis and genetic manipulation indicates that this variation arises from genetic differences in the neuromodulatory architecture of the egg-laying circuitry. We provide experimental evidence that while strong egg retention can decrease maternal fitness due to in utero hatching, it may enhance offspring protection and confer a competitive advantage. Therefore, natural variation in C. elegans egg-laying behaviour can alter an apparent trade-off between different fitness components across generations. Our findings highlight underappreciated diversity in C. elegans egg-laying behavior and shed light on its fitness consequences. This behavioral variation offers a promising model to elucidate the molecular changes in a simple neural circuit underlying evolutionary shifts between alternative egg-laying modes in invertebrates.
Assuntos
Proteínas de Caenorhabditis elegans , Caenorhabditis elegans , Animais , Caenorhabditis elegans/genética , Oviposição/genética , Oviparidade , Proteínas de Caenorhabditis elegans/genética , Evolução BiológicaRESUMO
The reproductive diversity of extant cartilaginous fishes (class Chondrichthyes) is extraordinarily broad, reflecting more than 400 million years of evolutionary history. Among their many notable reproductive specialisations are viviparity (live-bearing reproduction) and matrotrophy (maternal provision of nutrients during gestation). However, attempts to understand the evolution of these traits have yielded highly discrepant conclusions. Here, we compile and analyse the current knowledge on the evolution of reproductive diversity in Chondrichthyes with particular foci on the frequency, phylogenetic distribution, and directionality of evolutionary changes in their modes of reproduction. To characterise the evolutionary transformations, we amassed the largest empirical data set of reproductive parameters to date covering nearly 800 extant species and analysed it via a comprehensive molecular-based phylogeny. Our phylogenetic reconstructions indicated that the ancestral pattern for Chondrichthyes is 'short single oviparity' (as found in extant holocephalans) in which females lay successive clutches (broods) of one or two eggs. Viviparity has originated at least 12 times, with 10 origins among sharks, one in batoids, and (based on published evidence) another potential origin in a fossil holocephalan. Substantial matrotrophy has evolved at least six times, including one origin of placentotrophy, three separate origins of oophagy (egg ingestion), and two origins of histotrophy (uptake of uterine secretions). In two clades, placentation was replaced by histotrophy. Unlike past reconstructions, our analysis reveals no evidence that viviparity has ever reverted to oviparity in this group. Both viviparity and matrotrophy have arisen by a variety of evolutionary sequences. In addition, the ancestral pattern of oviparity has given rise to three distinct egg-laying patterns that increased clutch (brood) size and/or involved deposition of eggs at advanced stages of development. Geologically, the ancestral oviparous pattern arose in the Paleozoic. Most origins of viviparity and matrotrophy date to the Mesozoic, while a few that are represented at low taxonomic levels are of Cenozoic origin. Coupled with other recent work, this review points the way towards an emerging consensus on reproductive evolution in chondrichthyans while offering a basis for future functional and evolutionary analyses. This review also contributes to conservation efforts by highlighting taxa whose reproductive specialisations reflect distinctive evolutionary trajectories and that deserve special protection and further investigation.
Assuntos
Filogenia , Viviparidade não Mamífera , Animais , Feminino , Viviparidade não Mamífera/fisiologia , Reprodução/fisiologia , Evolução BiológicaRESUMO
BACKGROUND: Like other oviparous organisms, the gonotrophic cycle of mosquitoes is not complete until they have selected a suitable habitat to oviposit. In addition to the evolutionary constraints associated with selective oviposition behavior, the physiological demands relative to an organism's oviposition status also influence their nutrient requirement from the environment. Yet, studies that measure transmission potential (vectorial capacity or competence) of mosquito-borne parasites rarely consider whether the rates of parasite replication and development could be influenced by these constraints resulting from whether mosquitoes have completed their gonotrophic cycle. METHODS: Anopheles stephensi mosquitoes were infected with Plasmodium berghei, the rodent analog of human malaria, and maintained on 1% or 10% dextrose and either provided oviposition sites ('oviposited' herein) to complete their gonotrophic cycle or forced to retain eggs ('non-oviposited'). Transmission potential in the four groups was measured up to 27 days post-infection as the rates of (i) sporozoite appearance in the salivary glands ('extrinsic incubation period' or EIP), (ii) vector survival and (iii) sporozoite densities. RESULTS: In the two groups of oviposited mosquitoes, rates of sporozoite appearance and densities in the salivary glands were clearly dependent on sugar availability, with shorter EIP and higher sporozoite densities in mosquitoes fed 10% dextrose. In contrast, rates of appearance and densities in the salivary glands were independent of sugar concentrations in non-oviposited mosquitoes, although both measures were slightly lower than in oviposited mosquitoes fed 10% dextrose. Vector survival was higher in non-oviposited mosquitoes. CONCLUSIONS: Costs to parasite fitness and vector survival were buffered against changes in nutritional availability from the environment in non-oviposited but not oviposited mosquitoes. Taken together, these results suggest vectorial capacity for malaria parasites may be dependent on nutrient availability and oviposition/gonotrophic status and, as such, argue for more careful consideration of this interaction when estimating transmission potential. More broadly, the complex patterns resulting from physiological (nutrition) and evolutionary (egg-retention) trade-offs described here, combined with the ubiquity of selective oviposition behavior, implies the fitness of vector-borne pathogens could be shaped by selection for these traits, with implications for disease transmission and management. For instance, while reducing availability of oviposition sites and environmental sources of nutrition are key components of integrated vector management strategies, their abundance and distribution are under strong selection pressure from the patterns associated with climate change.
Assuntos
Anopheles , Malária , Mosquitos Vetores , Oviposição , Plasmodium berghei , Animais , Anopheles/fisiologia , Anopheles/parasitologia , Mosquitos Vetores/fisiologia , Mosquitos Vetores/parasitologia , Feminino , Malária/transmissão , Malária/parasitologia , Plasmodium berghei/fisiologia , Glândulas Salivares/parasitologia , Esporozoítos/fisiologia , Açúcares/metabolismo , CamundongosRESUMO
The present study analyzed the sexual development, sizes at maturity and morphometric relationships for both sexes of Sympterygia acuta and S. bonapartii, endemic of south-western Atlantic Ocean. The examined specimens were obtained through research cruises and commercial fishing trips, during 2011 and 2012, along the southern Brazilian coast, in latitudes ranging from 34°28'S to 31°29'S and at depths between 15 and 142 m. Significant differences (p<0.05) in S. bonapartii and in S acuta between sexes for the relationships total length (cm) - disc width (cm) and total length - total/eviscerated weight (g) respectively, demonstrated sexual dimorphism during the development in both species. The estimated size at maturity for males and females, respectively, were 46.1 and 44.7 cm, for S. acuta, and 58.4 and 59.9 cm, for S. bonapartii. A decrease in size at maturity for both sexes was observed in S. acuta and females of S. bonapartii of the southern coast of Brazil, respect to previous studies carried out over the last 30 years.
O presente estudo analisou o desenvolvimento sexual, os tamanhos de maturidade e as relações morfométricas para ambos os sexos das espécies Sympterygia acuta e S. bonapartii endêmica do sudoeste do Oceano Atlântico. Os indivíduos foram coletados em cruzeiros de investigação e viagens de pesca comercial durante 2011 e 2012 ao longo da costa do Sul do Brasil em latitudes que variam de 34°28'S a 31° 29'S, e em profundidades entre 15 e 142 m. Houve diferenças significativas entre sexos para S. bonapartii (p <0,05) e S acuta nas relações comprimento total (cm) - largura do disco (cm) e comprimento - peso total e comprimento total - peso eviscerado (g), demonstrando dimorfismo sexual durante o desenvolvimento em ambas as espécies.Os tamanhos estimados de maturação para machos e fêmeas, respectivamente, foram iguais a 46,1 e 44,7 cm para S. acuta; e 58,4 e 59,9 cm para S. bonapartii. Uma diminuição nos tamanhos de maturidade para ambos os sexos foi observada em S. acuta e fêmeas de S. bonapartii da costa Sul do Brasil, com relação a estudos realizados há 30 anos.