Urban Facilitation of Reproductive Biology and Body Size in Invasive Boa constrictor on Aruba

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Reproductive biology and annual reproductive cycles of two sympatric lineages of Bostrychus sinensis with a natural habitat on southeastern coast of China

Body size affects many aspects of an organism's performance, including reproduction. Ecologists have shown an increased interest in linkages between body size variation and population dynamics. Fecundity in a number of insect orders is often positively correlated with body weight or structural size, but reproductive characteristics and body size are not always positively correlated, particularly in field studies. Numerous biotic and environmental factors can influence individual body size and reproduction in grasshoppers under field conditions. Intraspecific relationships between reproductive traits and individual body size in melanopline grasshoppers were examined using data from four field experiments. Significant positive correlations between body size and reproductive traits occurred in three of four field experiments involving Melanoplus sanguinipes (Fabricius) and Phoetaliotes nebrascensis (Thomas) where per capita resource availability was manipulated, with a highly significant relationship between femur length and functional ovarian follicles when statistical results were combined from all correlations. In addition, individual femur length was a significant covariate for at least one reproductive trait in three experiments. Biotic factors such as food availability and predation could be more important than body size in determining reproductive output under field conditions, but further work is required to examine under what conditions individual body size affects reproduction in grasshoppers.

Sexual size dimorphism is ultimately the result of independent, sex-specific selection on body size. In mammals, male-biased sexual size dimorphism is the predominant pattern, and it is usually attributed to the polygynous mating system prevalent in most mammals. This sole explanation is unsatisfying because selection acts on both sexes simultaneously, therefore any explanation of sexual size dimorphism should explain why one sex is relatively large and the other is small. Using mark-recapture techniques and DNA microsatellite loci to assign parentage, we examined sex-specific patterns of annual reproductive success and survival in the yellow-pine chipmunk (Tamias amoenus), a small mammal with female-biased sexual size dimorphism, to test the hypothesis that the dimorphism was related to sex differences in the relationship between body size and fitness. Chipmunks were monitored and body size components measured over three years in the Kananaskis Valley, Alberta, Canada. Male reproductive success was independent of body size perhaps due to trade-offs in body size associated with behavioral components of male mating success: dominance and running speed. Male survival was consistent with stabilizing selection for overall body size and body size components. The relationship between reproductive success and female body size fluctuated. In two of three years the relationship was positive, whereas in one year the relationship was negative. This may have been the result of differences in environmental conditions among years. Large females require more energy to maintain their soma than small females and may be unable to maintain lactation in the face of challenging environmental conditions. Female survival was positively related to body size, with little evidence for stabilizing selection. Sex differences in the relationship between body size and fitness (reproductive success and survival) were the result of different processes, but were ultimately consistent with female-biased sexual size dimorphism evident in this species.

Sexual size dimorphism is ultimately the result of independent, sex-specific selection on body size. In mammals, male-biased sexual size dimorphism is the predominant pattern, and it is usually attributed to the polygynous mating system prevalent in most mammals. This sole explanation is unsatisfying because selection acts on both sexes simultaneously, therefore any explanation of sexual size dimorphism should explain why one sex is relatively large and the other is small. Using mark-recapture techniques and DNA microsatellite loci to assign parentage, we examined sex-specific patterns of annual reproductive success and survival in the yellow-pine chipmunk (Tamias amoenus), a small mammal with female-biased sexual size dimorphism, to test the hypothesis that the dimorphism was related to sex differences in the relationship between body size and fitness. Chipmunks were monitored and body size components measured over three years in the Kananaskis Valley, Alberta, Canada. Male reproductive success was independent of body size perhaps due to trade-offs in body size associated with behavioral components of male mating success: dominance and running speed. Male survival was consistent with stabilizing selection for overall body size and body size components. The relationship between reproductive success and female body size fluctuated. In two of three years the relationship was positive, whereas in one year the relationship was negative. This may have been the result of differences in environmental conditions among years. Large females require more energy to maintain their soma than small females and may be unable to maintain lactation in the face of challenging environmental conditions. Female survival was positively related to body size, with little evidence for stabilizing selection. Sex differences in the relationship between body size and fitness (reproductive success and survival) were the result of different processes, but were ultimately consistent with female-biased sexual size dimorphism evident in this species.

In this study, I investigated the reproductive biology of fish species from the family Characidae of the order Characiformes. I also investigated the relationship between reproductive biology and body weight and interpreted this relationship in a phylogenetic context. The results of the present study contribute to the understanding of the evolution of the reproductive strategies present in the species of this family. Most larger characid species and other characiforms exhibit a reproductive pattern that is generally characterized by a short seasonal reproductive period that lasts one to three months, between September and April. This is accompanied by total spawning, an extremely high fecundity, and, in many species, a reproductive migration. Many species with lower fecundity exhibit some form of parental care. Although reduction in body size may represent an adaptive advantage, it may also require evolutionary responses to new biological problems that arise. In terms of reproduction, smaller species have a tendency to reduce the number of oocytes that they produce. Many small characids have a reproductive pattern similar to that of larger characiforms. On the other hand they may also exhibit a range of modifications that possibly relate to the decrease in body size and the consequent reduction in fecundity. Examples of changes in the general reproductive pattern include the following: reduction in the size of mature oocytes; increase in fecundity; production of several batches of oocytes; an extended reproductive period or even continuous reproduction that allows individuals to reproduce more than once a year; high growth rates; rapid recruitment of juveniles; presence of more than one reproductive cohort that increases the sexually active population; and multiple independent development of insemination as a reproductive strategy. These changes are possibly associated with adaptive pressures that are related to the reduction in body size. In addition, such reproductive characteristics or novelties may reflect the phylogenetic history of a given species.

Spatial variation in body size and reproductive condition of subtidal mussels: Considerations for sustainable management

Annual reproductive cycle, age and body size at maturity, and potential and relative fecundity were examined in female willowy flounder in the North Pacific off Japan. Vitellogenesis became active from September, followed by the beginning of spawning in December. The spawning season continued until May with its peak in January. Estimated maturation rate was 50% at a standard length of 16 cm, 30% in 2-year-olds, and almost 100% in ≥3-year-old fish. Potential fecundity increased with age, while relative fecundity decreased in older fish. The results clarify some aspects of the detailed reproductive biology of female willowy flounder and emphasize the importance of age-composition data in estimating reproductive potential within a population.

In this study 57 specimens of the lizard Ameiva ameiva (Linnaeus, 1758) collected in the restinga at Barra de Maricá, in the state of Rio de Janeiro, southeastern Brazil, were analyzed to investigate size relations and reproduction (in females) and sexual dimorphism of this population. We answered the following questions: 1) what is the minimum reproductive body size in females? 2) what is the average clutch size and 3) how is clutch size related to body size? 4) Are body and head sizes sexually dimorphic? Mean clutch size was 6.7 ± 2.1 eggs and was positively correlated with female body size. Sexual dimorphism favoring males was found: adult mean snout-vent length was great in males (124.2 ± 17.8 mm) than females (96.5 ± 23.1 mm SVL), and males were larger with respect to head width and length, and body mass. Thus, despite the marked seasonality at Barra de Maricá, A. ameiva has an extended reproductive period. Also, intrasexual selection may have acted on females to produce larger clutches, and on males, favoring larger males.

To place associations among body size, age at maturity, age, and reproductive traits of a long‐lived organism in the context of current life history models based on the concept of norms of reaction, we examined data from a mark‐recapture study of Blanding's turtles (Emydoidea blandingi) in southeastern Michigan during 24 of the years between 1953 and 1988. Females matured between 14 and 20 years of age. Both the smallest and largest adult females in the population were reproducing for the first time in their lives. This result suggests that a combination of differences in juvenile growth rates and ages at maturity, and not indeterminate growth, are the primary cause of variation in body size among adults. Body size variation among individuals was not related to age at sexual maturity. Females that had slower growth rates as juveniles matured later at similar mean body size compared to those with more rapid growth that matured at an earlier age. As a result, a linear model of age at sexual maturity with growth rates of primiparous females between hatching and maturity was significant and negative (R2 = 0.76). Frequency of reproduction of the largest and smallest females was not significantly different. Clutch size did not vary significantly with age among either primiparous or multiparous females. Clutch sizes of primiparous females and multiparous females were not significantly different. However, older females (>55 years minimum age) reproduced more frequently than did younger females (minimum age <36 y).

Sexual maturation and allometry of reproductive traits in large- and small-sized male honeybees

It has been hypothesized that mobile species should be more negatively affected by road mortality than less-mobile species because they interact with roads more often, and that species with lower reproductive rates and longer generation times should be more susceptible to road effects because they will be less able to rebound quickly from population declines. Taken together, these hypotheses suggest that, in general, larger species should be more affected by road networks than smaller species because larger species generally have lower reproductive rates and longer generation times and are more mobile than smaller species. We tested these hypotheses by estimating relative abundances of 17 mammal species across landscapes ranging in road density within eastern Ontario, Canada. For each of the 13 species for which detectability was not related to road density, we quantified the relationship between road density and relative abundance. We then tested three cross-species predictions: that the slope of the relationship between road density and abundance should become increasingly negative with (1) decreasing annual reproductive rate; (2) increasing home range area (an indicator of movement range); and (3) increasing body size. All three predictions were supported in univariate models, with R2 values of 0.68, 0.50, and 0.52 respectively. The best overall model based on AICc contained both reproductive rate (P = 0.008) and body size (P = 0.072) and explained 77% of the variation in the slope of the relationship between road density and abundance. Our results suggest that priority should be placed on mitigating road effects on large mammals with low reproductive rates.

In salmonid fishes, the tendency to return to the natal site for breeding leads to reproductively isolated, locally adapted populations. In addition to this isolation-by-space, the heritability of breeding date can result in temporal segregation or isolation of breeding units. We examined the interaction between breeding location (spatial segregation) and arrival date (temporal segregation) for two fitness-related traits, reproductive life span and body size, of sockeye salmon ( Oncorhynchus nerka (Walbaum in Artedi, 1792)) in a small Alaskan stream. Analysis of data on tagged individuals over 9 years revealed that both males and females arriving early to the spawning grounds tended to spawn farther upstream than those arriving later, demonstrating the potential for segregation in time and space within the population. Both body length and reproductive life span also consistently varied with arrival date. Larger males and females entered the stream before smaller individuals, and individuals of both sexes that arrived early lived longer in the stream than those that arrived later. However, neither reproductive life span nor body size varied significantly with breeding location, indicating that the linkage between spatial and temporal structure in this breeding population is incomplete, and that segregation in time may currently be the dominant component of within-population structure.

Terrestrial breeding is a derived condition in frogs, with multiple transitions from an aquatic ancestor. Shifts in reproductive mode often involve changes in habitat use, and these are typically associated with diversification in body plans, with repeated transitions imposing similar selective pressures. We examine the diversification of reproductive modes, male and female body sizes, and sexual size dimorphism (SSD) in the Neotropical frog genera Cycloramphus and Zachaenus, both endemic to the Atlantic rainforest of Brazil. Species in this clade either breed in rocky streams (saxicolous) or in terrestrial environments, allowing us to investigate reproductive habitat shifts. We constructed a multilocus molecular phylogeny and inferred evolutionary histories of reproductive habitats, body sizes, and SSD. The common ancestor was small, saxicolous, and had low SSD. Terrestrial breeding evolved independently three times and we found a significant association between reproductive habitat and SSD, with shifts to terrestrial breeding evolving in correlation with decreases in male body size, but not female body size. Terrestrial breeding increases the availability of breeding sites and results in concealment of amplexus, egg-laying, and parental care, therefore reducing male-male competition at all stages of reproduction. We conclude that correlated evolution of terrestrial reproduction and small males is due to release from intense male-male competition that is typical of exposed saxicolous breeding.

Island and mainland populations of animal species often differ strikingly in life‐history traits such as clutch size, egg size, total reproductive effort and body size. However, despite widespread recognition of insular shifts in these life‐history traits in birds, mammals and reptiles, there have been no reports of such life‐history shifts in amphibians. Furthermore, most studies have focused on one specific life‐history trait without explicit consideration of coordinated evolution among these intimately linked life‐history traits, and thus the relationships among these traits are poorly studied. Here we provide the first evidence of insular shifts and trade‐offs in a coordinated suite of life‐history traits for an amphibian species, the pond frog Rana nigromaculata. Life‐history data were collected from eight islands in the Zhoushan Archipelago and neighboring mainland China. We found consistent, significant shifts in all life‐history traits between mainland and island populations. Island populations had smaller clutch sizes, larger egg sizes, larger female body size and invested less in total reproductive effort than mainland populations. Significant negative relationships were found between egg size and clutch size and between egg size and total reproductive effort among frog populations after controlling for the effects of body size. Therefore, decreased reproductive effort and clutch size, larger egg size and body size in pond frogs on islands were selected through trade‐offs as an overall life‐history strategy. Our findings contribute to the formation of a broad, repeatable ecological generality for insular shifts in life‐history traits across a range of terrestrial vertebrate taxa.