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Discussion (Chapter on reproductive endocrinology: The hypothalamo-hypophysial axis)
No abstract available.
Effects of fishing on the reproductive capacity of striped bass in Chesapeake Bay, Maryland
No abstract available at this time
Reproduction in temperate freshwater and estuarine fishes
No abstract available at this time
Successful experimental reproduction of early mortality syndrome in Lake trout: Research task report on early mortality syndrome workshop
No abstract available at this time
Mercury in birds of the San Francisco Bay-Delta: trophic pathways, bioaccumulation and ecotoxicological risk to avian reproduction
No abstract available at this time
Cottontail reproduction related to dieldrin exposure.
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Predator avoidance performance of larval fathead minnows (Pimephales promelas) following short-term exposure to estrogen mixtures
Aquatic organisms exposed to endocrine disrupting compounds (EDCs) at early life-stages may have reduced reproductive fitness via disruption of reproductive and non-reproductive behavioral and physiological pathways. Survival to reproductive age relies upon optimal non-reproductive trait expression, such as adequate predator avoidance responses, which may be impacted through EDC exposure. During a predator–prey confrontation, larval fish use an innate C-start escape behavior to rapidly move away from an approaching threat. We tested the hypotheses that (1) larval fathead minnows exposed to estro gens, a primary class of EDCs, singularly or in mixture, suffer a reduced ability to perform an innate C-start behavior when faced with a threat stimulus; (2) additive effects will cause greater reductions in C-start behavior; and (3) effects will differ among developmental stages. In this study, embryos (post-fertilization until hatching) were exposed for 5 days to environmentally relevant concentrations of estrone (E1), 17-estradiol (E2), and 17-ethinylestradiol (EE2) singularly and in mixture. Exposed embryos were allowed to hatch and grow in control well water until 12 days old. Similarly, post-hatch fathead minnows were exposed for 12 days to these compounds. High-speed (1000 frames/s) video recordings of escape behavior were collected and transferred to National Institutes of Health Image for frame-by-frame anal- ysis of latency period, escape velocity, and total escape response (combination of latency period and escape velocity). When tested 12 days post-hatch, only E1 adversely affected C-start performance of larvae exposed as embryos. Conversely, larvae exposed for 12 days post-hatch did not exhibit altered escape responses when exposed to E1, while adverse responses were seen in E2 and the estrogen mixture. Ethinylestradiol exposure did not elicit changes in escape behaviors at either developmental stage. The direct impact of reduced C-start performance on survival, and ultimately, reproductive fitness provides an avenue to assess the ecological relevance of exposure in an assay of relatively short duration.
Variation in the vital rates of an Antarctic marine predator: the role of individual heterogeneity
Variation in life‐history traits such as lifespan and lifetime reproductive output is thought to arise, in part, due to among‐individual differences in the underlying probabilities of survival and reproduction. However, the stochastic nature of demographic processes can also generate considerable variation in fitness‐related traits among otherwise‐identical individuals. An improved understanding of life‐history evolution and population dynamics therefore depends on evaluating the relative role of each of these processes. Here, we used a 33‐yr data set with reproductive histories for 1,274 female Weddell seals from Erebus Bay, Antarctica, to assess the strength of evidence for among‐individual heterogeneity in the probabilities of survival and reproduction, while accounting for multiple other sources of variation in vital rates. Our analysis used recent advances in Bayesian model selection techniques and diagnostics to directly compare model fit and predictive power between models that included individual effects on survival and reproduction to those that did not. We found strong evidence for costs of reproduction to both survival and future reproduction, with breeders having rates of survival and subsequent reproduction that were 3% and 6% lower than rates for non‐breeders. We detected age‐related changes in the rates of survival and reproduction, but the patterns differed for the two rates. Survival rates steadily declined from 0.92 at age 7 to 0.56 at the maximal age of 31 yr. In contrast, reproductive rates increased from 0.68 at age 7 to 0.79 at age 16 and then steadily declined to 0.37 for the oldest females. Models that included individual effects explained more variation in observed life histories and had better estimated predictive power than those that did not, indicating their importance in understanding sources of variation among individuals in life‐history traits. We found that among‐individual heterogeneity in survival was small relative to that for reproduction. Our study, which found patterns of variation in vital rates that are consistent with a series of predictions from life‐history theory, is the first to provide a thorough assessment of variation in important vital rates for a long‐lived, high‐latitude marine mammal while taking full advantage of recent developments in model evaluation.
Neuroendocrine and behavioral implications of endocrine disrupting chemicals in quail
Studies in our laboratory have focused on endocrine, neuroendocrine, and behavioral components of reproduction in the Japanese quail. These studies considered various stages in the life cycle, including embryonic development, sexual maturation, adult reproductive function, and aging. A major focus of our research has been the role of neuroendocrine systems that appear to synchronize both endocrine and behavioral responses. These studies provide the basis for our more recent research on the impact of endocrine disrupting chemicals (EDCs) on reproductive function in the Japanese quail. These endocrine active chemicals include pesticides, herbicides, industrial products, and plant phytoestrogens. Many of these chemicals appear to mimic vertebrate steroids, often by interacting with steroid receptors. However, most EDCs have relatively weak biological activity compared to native steroid hormones. Therefore, it becomes important to understand the mode and mechanism of action of classes of these chemicals and sensitive stages in the life history of various species. Precocial birds, such as the Japanese quail, are likely to be sensitive to EDC effects during embryonic development, because sexual differentiation occurs during this period. Accordingly, adult quail may be less impacted by EDC exposure. Because there are a great many data available on normal development and reproductive function in this species, the Japanese quail provides an excellent model for examining the effects of EDCs. Thus, we have begun studies using a Japanese quail model system to study the effects of EDCs on reproductive endocrine and behavioral responses. In this review, we have two goals: first, to provide a summary of reproductive development and sexual differentiation in intact Japanese quail embryos, including ontogenetic patterns in steroid hormones in the embryonic and maturing quail. Second, we discuss some recent data from experiments in our laboratory in which EDCs have been tested in Japanese quail. The Japanese quail provides an excellent avian model for testing EDCs because this species has well-characterized reproductive endocrine and behavioral responses. Considerable research has been conducted in quail in which the effects of embryonic steroid exposure have been studied relative to reproductive behavior. Moreover, developmental processes have been studied extensively and include investigations of the reproductive axis, thyroid system, and stress and immune responses. We have conducted a number of studies, which have considered long-term neuroendocrine consequences as well as behavioral responses to steroids. Some of these studies have specifically tested the effects of embryonic steroid exposure on later reproductive function in a multigenerational context. A multigenerational exposure provides a basis for understanding potential exposure scenarios in the field. In addition, potential routes of exposure to EDCs for avian species are being considered, as well as differential effects due to stage of the life cycle at exposure to an EDC. The studies in our laboratory have used both diet and egg injection as modes of exposure for Japanese quail. In this way, birds were exposed to a specific dose of an EDC at a selected stage in development by injection. Alternatively, dietary exposure appears to be a primary route of exposure; therefore experimental exposure through the diet mimics potential field situations. Thus, experiments should consider a number of aspects of exposure when attempting to replicate field exposures to EDCs.
Territory occupancy and breeding success of Peregrine Falcons Falco peregrinus at various stages of population recovery
Organochlorine pesticides disrupted reproduction and killed many raptorial birds, and contributed to population declines during the 1940s to 1970s. We sought to discern whether and to what extent territory occupancy and breeding success changed from the pesticide era to recent years in a resident population of Peregrine Falcons Falco peregrinus in southern Scotland using long-term (1964–2015) field data and multi-state, multi-season occupancy models. Peregrine territories that were occupied with successful reproduction in one year were much more likely to be occupied and experience reproductive success in the following year, compared with those that were unoccupied or occupied by unsuccessful breeders in the previous year. Probability of territory occupancy differed between territories in the eastern and western parts of the study area, and varied over time. The probability of occupancy of territories that were unoccupied and those that were occupied with successful reproduction during the previous breeding season generally increased over time, whereas the probability of occupancy of territories that were occupied after failed reproduction decreased. The probability of reproductive success (conditional on occupancy) in territories that were occupied during the previous breeding season increased over time. Specifically, for territories that had been successful in the previous year, the probability of occupancy as well as reproductive success increased steadily over time; these probabilities were substantially higher in recent years than earlier, when the population was still exposed to direct or residual effects of organochlorine pesticides. These results are consistent with the hypothesis that progressive reduction, followed by a complete ban, in the use of organochlorine pesticides improved reproductive success of Peregrines in southern Scotland. Differences in the temporal pattern of probability of reproductive success between south-eastern and south-western Scotland suggest that the effect of organochlorine pesticides on Peregrine reproductive success and/or the recovery from pesticide effects varied geographically and was possibly affected by other factors such as persecution.
Gonad organochlorine concentrations and plasma steroid levels in white sturgeon (Acipenser transmontanus) from the Columbia River, USA
Sturgeon are an important fishery resource world-wide, providing food and income through commercial, sport, and tribal fisheries. However, sturgeon populations are imperiled in many areas due to overharvest, habitat loss, and pollution. White Sturgeon ( Acipenser transmontanus ) are found along the west coast of North America from San Francisco Bay, USA to British Columbia, Canada. The Columbia River, located in the Pacific Northwest USA, supports active commercial, sport, and tribal white sturgeon fisheries. The white sturgeon fishery in the Columbia River estuary is one of the most productive sturgeon fisheries in the World. Despite the success of the Columbia River estuary white sturgeon fishery, the populations within the impounded sections (i.e. behind the hydroelectric dams) of the Columbia River experience poor reproductive success (Beamesderfer et al. 1995). This poor reproductive success has been attributed to hydroelectric development, but water pollution could also be a significant factor. The bottom dwelling life history and late maturing reproductive strategy for this species may make it particularly sensitive to the adverse effects of bioaccumulative pollutants. The Columbia River receives effluent from bleached-kraft pulp mills, aluminum smelters, municipal sewage treatment plants and runoff from agricultural. industrial, and urban areas. Bioaccumulative contaminants that have the potential for endocrine disruption have been detected in fish and sediments from the Columbia River (Foster et al. 1999). An integrated system of hormones control reproduction in vertebrates. Plasma steroids direct developmental events essential for reproduction. Disruption of endocrine control by contaminants has been linked to reproductive anomalies and failure in a number of vertebrate species (Guillette et al. 1996; Jobling et al. 1996). Because of this, it is important to understand if organochlorine compounds are accumulating in Columbia River white sturgeon and having an effect on their reproductive physiology. The objective of this study was to determine if sturgeon from an impounded section of the Columbia River (where reproductive success has been low) had higher levels of bioaccumulative pollutants than sturgeon from the estuary (where reproductive success has been high) and if these compounds were associated with decreased plasma steroid levels. Specifically, we measured chlorinated pesticides and PCBs in the gonads and plasma steroids in white sturgeon from the Columbia River fishery.
Demographic mechanisms of snowshoe hare population cycles in Yukon, Canada
One hundred years have elapsed since Charles Elton (1924) described the periodic fluctuations in North American snowshoe hare abundance, yet mechanisms underlying 9–11-year population cycles in snowshoe hares continue to be debated. We applied multistate capture–mark–recapture models to long-term field data (1977–2020) based on >20,000 captures of >7000 unique snowshoe hares ( Lepus americanus ) from Kluane Lake, Yukon, Canada, to estimate and model state-specific demographic parameters. Juveniles had the lowest and reproductive adult females the highest apparent survival. Apparent survival of all sex-age classes was highest during the mid- and late-breeding seasons and was generally better during the increase phase. Conditional probability of females transitioning from non-reproductive to reproductive state, and reproductive females remaining in the reproductive state, increased substantially as the population transitioned from low to increase phase throughout the breeding season. Analysis of stage-structured matrix population models revealed that population-dynamic characteristics were strongly phase-specific, and also varied across seasons, with the increase phases being characterized by high monthly asymptotic population growth rate. Snowshoe hares experienced short stage-specific generation time during the early breeding season across all phases; they experienced relatively long generation time during the increase and low phase of the mid-breeding season, and the increase and peak phase of the late breeding season. Elasticity analyses showed that asymptotic population growth rate was proportionately most sensitive to changes in survival of adult females across all phases and seasons. However, retrospective life table response experiment analysis showed that rapid growth of the snowshoe hare populations during the increase phase was due to improvements in reproductive transitions and pre-weaning survival, whereas population declines are caused primarily by reduced survival (primarily, pre-weaning survival), with reduced reproductive transitions and smaller litter sizes playing a secondary role. Our results suggest that cyclic populations of snowshoe hares are characterized by complex demographic and population-dynamic patterns, depending on phase of the cycle and reproductive season, and that different demographic mechanisms underlie rapid population growth during the increase phase, and swift population declines as the population transitions from the peak to the decline phase. Because our study represents the first comprehensive demographic and population-dynamic study of a cyclic population, similar studies would be needed to test the generalities of our conclusions. Whereas density-dependent predation has been shown to be the primary cause of phase-related changes in survival, future research should focus on identifying mechanisms underlying phase-related changes in reproductive parameters.
Population dynamics of spotted owls in the Sierra Nevada, California
The California spotted owl (Strix occidentalis occidentalis) is the only spotted owl subspecies not listed as threatened or endangered under the United States Endangered Species Act despite petitions to list it as threatened. We conducted a meta-analysis of population data for 4 populations in the southern Cascades and Sierra Nevada, California, USA, from 1990 to 2005 to assist a listing evaluation by the United States Fish and Wildlife Service. Our study areas (from N to S) were on the Lassen National Forest (LAS), Eldorado National Forest (ELD), Sierra National Forest (SIE), and Sequoia and Kings Canyon National Parks (SKC). These study areas represented a broad spectrum of habitat and management conditions in these mountain ranges. We estimated apparent survival probability, reproductive output, and rate of population change for spotted owls on individual study areas and for all study areas combined (meta-analysis) using model selection or model-averaging based on maximum-likelihood estimation. We followed a formal protocol to conduct this analysis that was similar to other spotted owl meta-analyses. Consistency of field and analytical methods among our studies reduced confounding methodological effects when evaluating results. We used 991 marked spotted owls in the analysis of apparent survival. Apparent survival probability was higher for adult than for subadult owls. There was little difference in apparent survival between male and female owls. Model-averaged mean estimates of apparent survival probability of adult owls varied from 0.811 ?? 0.021 for females at LAS to 0.890 ?? 0.016 for males at SKC. Apparent survival increased over time for owls of all age classes at LAS and SIE, for adults at ELD, and for second-year subadults and adults at SKC. The meta-analysis of apparent survival, which included only adult owls, confirmed an increasing trend in survival over time. Survival rates were higher for owls on SKC than on the other study areas. We analyzed data from 1,865 observations of reproductive outcomes for female spotted owls. The proportion of subadult females among all territorial females of known age ranged from 0.00 to 0.25 among study areas and years. The proportion of subadults among female spotted owls was negatively related to reproductive output (no. of young fledged/territorial F owl) for ELD and SIE. Eldorado study area and LAS showed an alternate-year trend in reproductive output, with higher output in even-numbered years. Mean annual reproductive output was 0.988 ?? 0.154 for ELD, 0.624 ?? 0.140 for LAS, 0.478 ?? 0.106 for SIE, and 0.555 ?? 0.110 for SKC. Eldorado Study Area exhibited a declining trend and the greatest variation in reproductive output over time, whereas SIE and SKC, which had the lowest reproductive output, had the lowest temporal variation. Meta-analysis confirmed that reproductive output varied among study areas. Reproductive output was highest for adults, followed by second-year subadults, and then by first-year subadults. We used 842 marked subadult and adult owls to estimate population rate of change. Modeling indicated that ??t (??t is the finite rate of population change estimated using the reparameterized JollySeber estimator Pradel 1996) was either stationary (LAS and SIE) or increasing after an initial decrease (ELD and SKC). Mean estimated ??t for the 4 study areas was 1.007 (95 CI 0.9521.066) for ELD; 0.973 (95 CI 0.9461.001) for LAS; 0.992 (95 CI 0.9661.018) for SIE; and 1.006 (95 CI 0.9471.068) for SKC. The best meta-analysis model of population trend indicated that ?? varied across time but was similar in trend among the study areas. Our estimates of realized population change (??t; Franklin et al. 2004), which we estimated as the product 1 ?? ??3 ?? ??4 ?? .?? ??k -1, were based on estimates of ??t from individual study areas and did not require estimating annual population size for each study area. Trends represented the proportion of the population size in the first ye
Identification and synthetic modeling of factors affecting American black duck populations
We reviewed the literature on factors potentially affecting the population status of American black ducks ( Anas rupribes ). Our review suggests that there is some support for the influence of 4 major, continental-scope factors in limiting or regulating black duck populations: 1) loss in the quantity or quality of breeding habitats; 2) loss in the quantity or quality of wintering habitats; 3) harvest, and 4) interactions (competition, hybridization) with mallards ( Anas platyrhychos ) during the breeding and/or wintering periods. These factors were used as the basis of an annual life cycle model in which reproduction rates and survival rates were modeled as functions of the above factors, with parameters of the model describing the strength of these relationships. Variation in the model parameter values allows for consideration of scientific uncertainty as to the degree each of these factors may be contributing to declines in black duck populations, and thus allows for the investigation of the possible effects of management (e.g., habitat improvement, harvest reductions) under different assumptions. We then used available, historical data on black duck populations (abundance, annual reproduction rates, and survival rates) and possible driving factors (trends in breeding and wintering habitats, harvest rates, and abundance of mallards) to estimate model parameters. Our estimated reproduction submodel included parameters describing negative density feedback of black ducks, positive influence of breeding habitat, and negative influence of mallard densities; our survival submodel included terms for positive influence of winter habitat on reproduction rates, and negative influences of black duck density (i.e., compensation to harvest mortality). Individual models within each group (reproduction, survival) involved various combinations of these factors, and each was given an information theoretic weight for use in subsequent prediction. The reproduction model with highest AIC weight (0.70) predicted black duck age ratios increasing as a function of decreasing mallard abundance and increasing acreage of breeding habitat; all models considered involved negative density dependence for black ducks. The survival model with highest AIC weight (0.51) predicted nonharvest survival increasing as a function of increasing acreage of wintering habitat and decreasing harvest rates (additive mortality); models involving compensatory mortality effects received ≈0.12 total weight, vs. 0.88 for additive models. We used the combined model, together with our historical data set, to perform a series of 1-year population forecasts, similar to those that might be performed under adaptive management. Initial model forecasts over-predicted observed breeding populations by ≈25%. Least-squares calibration reduced the bias to ≈0.5% under prediction. After calibration, model-averaged predictions over the 16 alternative models (4 reproduction × 4 survival, weighted by AIC model weights) explained 67% of the variation in annual breeding population abundance for black ducks, suggesting that it might have utility as a predictive tool in adaptive management. We investigated the effects of statistical uncertainty in parameter values on predicted population growth rates for the combined annual model, via sensitivity analyses. Parameter sensitivity varied in relation to the parameter values over the estimated confidence intervals, and in relation to harvest rates and mallard abundance. Forecasts of black duck abundance were extremely sensitive to variation in parameter values for the coefficients for breeding and wintering habitat effects. Model-averaged forecasts of black duck abundance were also sensitive to changes in harvest rate and mallard abundance, with rapid declines in black duck abundance predicted for a range of harvest rates and mallard abundance higher than current levels of either factor, but easily envisaged, particularly given current rates of growth for mallard populations. Because of concerns about sensitivity to habitat coefficients, and particularly in light of deficiencies in the historical data used to estimate these parameters, we developed a simplified model that excludes habitat effects. We also developed alternative models involving a calibration adjustment for reproduction rates, survival rates, or neither. Calibration of survival rates performed best (AIC weight 0.59, % BIAS = -0.280, R 2 =0.679), with reproduction calibration somewhat inferior (AIC weight 0.41, % BIAS = -0.267, R 2 =0.672); models without calibration received virtually no AIC weight and were discarded. We recommend that the simplified model set (4 biological models × 2 alternative calibration factors) be retained as the best working set of alternative models for research and management. Finally, we provide some preliminary guidance for the development of adaptive harvest management for black ducks, using our working set of models.