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Spatiotemporal ecology of Apalone spinifera in a large, Great Plains river ecosystem

Sparse information exists about the ecology of Spiny Softshell Turtles (Apalone spinifera) in large rivers, at the northwestern extent of their natural range, and in Montana, where they are disjunct from downstream populations and a State Species of Concern. We determined spatiotemporal ecology of 47 female and 12 male turtles from 2009 through 2012 and identified fundamental habitats in the Missouri River in east-central Montana. Movement rates of females were greater than those of males and peaked before nesting. Movement rates of males peaked before overwintering, and movement rates of both sexes were minimal in winter. Home range sizes were not different between sexes, varied among individuals and seasons, and were similar to those reported elsewhere in their northern range. Turtles aggregated and showed interannual fidelity to separate and disparate habitats in different seasons. Turtles often chose fine substrates, tributary confluences, and reaches with islands during summer and mainstem outside bends in the winter. They inhabited shallow, slow water velocity areas from May to September. They inhabited deeper, moderate velocity areas from October to April. We did not observe ice jams and associated riverbed scour at hibernacula, but did observe them elsewhere. Ice jams may be spatially predictable and influence the distribution of riverine turtles during autumn and winter. Preservation of dissimilar habitats used during major portions of the life cycle (lateral habitats, islands, and hibernacula) and natural streamflow patterns, which influenced timing of habitat availability and turtle movement, may facilitate continued existence of Spiny Softshell Turtles in the Missouri River in Montana

Herpetological Conservation and Biology↗

Sampling and analysis frameworks for inference in ecology

1. Reliable statistical inference is central to ecological research, much of which seeks to estimate population attributes and their interactions. The issue of sampling design and its relationship to inference has become increasingly important due to rapid proliferation of modeling methodology (line transect modeling, capture-recapture, estimation of occurrence, model selection procedures, hierarchical modeling) and new sampling approaches (adaptive sampling, other specialized designs). It is important for ecologists using these advanced methods to be aware of how the linkages between sample selection and data analysis can potentially affect inference. 2. We examine design-based and model-based inference frameworks for ecological data collected randomly, purposively, or opportunistically. We elucidate differences in the probability structures for data arising from these frameworks, clarify the assumptions that underlie them, and demonstrate their differences. 3. Design-based inference builds on a probability structure inherited from randomized data collection, whereas model-based inference relies on an assumed stochastic model of the data. By itself, a design-based approach is of limited value for inferences about causal hypotheses. In contrast, model-based inference is dependent on a conditionality principle that can seldom be shown to be met for an ecological system. We describe the conditions under which one can safely ignore sampling design in model-based analysis, along with inferential implications if these conditions are not met. The special case of opportunistic sampling is discussed. 4. We present a combined framework that takes advantage of both approaches to inference, and provides a robust methodology that can deal with the modeling of sampling problems such as nondetection and misclassification, as well as the exploration of causal hypotheses. The combined framework can be useful for identifying optimal sampling strategies. 5. Each approach to inference has its strengths and weaknesses, and practitioners should be aware of these in order to tailor designs and analyses to specific questions. We use the approaches and their underlying rationales to provide guidelines for choosing designs and estimators for reliable inference.

Methods in Ecology and Evolution↗

Population dynamics of Greater Scaup breeding on the Yukon-Kuskokwim Delta, Alaska

Populations of greater scaup ( Aythya marila ) remained relatively stable during a period when populations of lesser scaup ( A. affinis ) have declined from historic levels. To assist in describing these differences in population trends, from 1991 through 2000, we studied the survival, nesting ecology, and productivity of greater scaup on the Yukon-Kuskokwim Delta (Y-K Delta), Alaska, to develop a model of population dynamics. We located nests, radio-marked females for renesting studies, estimated duckling survival, and leg-banded females to examine nest site fidelity and annual survival. Greater scaup initiated egg laying later than other species, and most clutches (>80%) were initiated over 20 days each year. We located 1,056 nests; nest success ranged from 7 to 61 % among years. Following loss of their first clutch, 51 % of radio-tagged females attempted to renest. Duckling survival to 30 days of age was 37.5%. Our best model suggested that annual survival did not vary among years and averaged 81 %. Survival rate was positively related to structural body size. Only 8 of 214 banded individuals were reported as recovered (1 each in Maryland, Michigan, Minnesota, Washington, and Alaska and 3 in California). Using a stochastic model, we estimated that, on average, breeding females produced 0.57 young females/nesting season. We combined this estimate of productivity with our annual estimates of adult survival and an assumed population growth rate of 1.0, then solved for an estimate of first-year survival (0.40). Under these conditions the predicted stable age distribution of breeding females (i.e., the nesting population) was 15.1% 1-year-old, 4.1% 2-year-old first-time breeders, and 80.8% 2-year-old and older, experienced breeders. We subjected this stochastic model to perturbation analyses to examine the relative effects of demographic parameters on k. The relative effects of productivity and adult survival on the population growth rate were 0.26 and 0.72, respectively. Thus, compared to productivity, proportionally equivalent changes in annual survival would have 2.8 times the effect on k. However, when we examined annual variation in predicted population size using standardized regression coefficients, productivity explained twice as much variation as annual survival. Thus, management actions focused on changes in survival or productivity have the ability to influence population size; however, substantially larger changes in productivity are required to influence population trends.

Wildlife Monographs↗

Microsatellites: Evolutionary and methodological background and empirical applications at individual, population, and phylogenetic levels

The recent proliferation and greater accessibility of molecular genetic markers has led to a growing appreciation of the ecological and evolutionary inferences that can be drawn from molecular characterizations of individuals and populations (Burke et al. 1992, Avise 1994). Different techniques have the ability to target DNA sequences which have different patterns of inheritance, different modes and rates of evolution and, concomitantly, different levels of variation. In the quest for 'the right marker for the right job', microsatellites have been widely embraced as the marker of choice for many empirical genetic studies. The proliferation of microsatellite loci for various species and the voluminous literature compiled in very few years associated with their evolution and use in various research applications, exemplifies their growing importance as a research tool in the biological sciences. The ability to define allelic states based on variation at the nucleotide level has afforded unparalleled opportunities to document the actual mutational process and rates of evolution at individual microsatellite loci. The scrutiny to which these loci have been subjected has resulted in data that raise issues pertaining to assumptions formerly stated, but largely untestable for other marker classes. Indeed this is an active arena for theoretical and empirical work. Given the extensive and ever-increasing literature on various statistical methodologies and cautionary notes regarding the uses of microsatellites, some consideration should be given to the unique characteristics of these loci when determining how and under what conditions they can be employed.

Book chapter↗

Effect of dispersal at range edges on the structure of species ranges

Range edges are of particular interest to ecology because they hold key insights into the limits of the realized niche and associated population dynamics. A recent feature of Oikos summarized the state of the art on range edge ecology. While the typical question is what causes range edges, another important question is how range edges influence the distribution of abundances across a species geographic range when dispersal is present. We used a single species population dynamics model on a coupled-lattice to determine the effects of dispersal on peripheral populations as compared to populations at the core of the range. In the absence of resource gradients, the reduced neighborhood and thus lower connectivity or higher isolation among populations at the range edge alone led to significantly lower population sizes in the periphery of the range than in the core. Lower population sizes mean higher extinction risks and lower adaptability at the range edge, which could inhibit or slow range expansions, and thus effectively stabilize range edges. The strength of this effect depended on the potential population growth rate and the maximum dispersal distance. Lower potential population growth rates led to a stronger effect of dispersal resulting in a higher difference in population sizes between the two areas. The differential effect of dispersal on population sizes at the core and periphery of the range in the absence of resource gradients implies that traditional, habitat-based distribution models could result in misleading conclusions about the habitat quality in the periphery. Lower population sizes at the periphery are also relevant to conservation, because habitat removal not only eliminates populations but also creates new edges. Populations bordering these new edges may experience declines, due to their increased isolation. ?? OIKOS.

Oikos↗

Arctic biodiversity: Increasing richness accompanies shrinking refugia for a cold-associated tundra fauna

As ancestral biodiversity responded dynamically to late-Quaternary climate changes, so are extant organisms responding to the warming trajectory of the Anthropocene. Ecological predictive modeling, statistical hypothesis tests, and genetic signatures of demographic change can provide a powerful integrated toolset for investigating these biodiversity responses to climate change, and relative resiliency across different communities. Within the biotic province of Beringia, we analyzed specimen localities and DNA sequences from 28 mammal species associated with boreal forest and Arctic tundra biomes to assess both historical distributional and evolutionary responses and then forecasted future changes based on statistical assessments of past and present trajectories, and quantified distributional and demographic changes in relation to major management regions within the study area. We addressed three sets of hypotheses associated with aspects of methodological, biological, and socio-political importance by asking (1) what is the consistency among implications of predicted changes based on the results of both ecological and evolutionary analyses; (2) what are the ecological and evolutionary implications of climate change considering either total regional diversity or distinct communities associated with major biomes; and (3) are there differences in management implications across regions? Our results indicate increasing Arctic richness through time that highlights a potential state shift across the Arctic landscape. However, within distinct ecological communities, we found a predicted decline in the range and effective population size of tundra species into several discrete refugial areas. Consistency in results based on a combination of both ecological and evolutionary approaches demonstrates increased statistical confidence by applying cross-discipline comparative analyses to conservation of biodiversity, particularly considering variable management regimes that seek to balance sustainable ecosystems with other anthropogenic values. Refugial areas for cold-adapted taxa appear to be persistent across both warm and cold climate phases and although fragmented, constitute vital regions for persistence of Arctic mammals.

Ecosphere↗

Arctic climate change and its impacts on the ecology of the North Atlantic

Arctic climate change from the Paleocene epoch to the present is reconstructed with the objective of assessing its recent and future impacts on the ecology of the North Atlantic. A recurring theme in Earth's paleoclimate record is the importance of the Arctic atmosphere, ocean, and cryosphere in regulating global climate on a variety of spatial and temporal scales. A second recurring theme in this record is the importance of freshwater export from the Arctic in regulating global- to basin-scale ocean circulation patterns and climate. Since the 1970s, historically unprecedented changes have been observed in the Arctic as climate warming has increased precipitation, river discharge, and glacial as well as sea-ice melting. In addition, modal shifts in the atmosphere have altered Arctic Ocean circulation patterns and the export of freshwater into the North Atlantic. The combination of these processes has resulted in variable patterns of freshwater export from the Arctic Ocean and the emergence of salinity anomalies that have periodically freshened waters in the North Atlantic. Since the early 1990s, changes in Arctic Ocean circulation patterns and freshwater export have been associated with two types of ecological responses in the North Atlantic. The first of these responses has been an ongoing series of biogeographic range expansions by boreal plankton, including renewal of the trans-Arctic exchanges of Pacific species with the Atlantic. The second response was a dramatic regime shift in the shelf ecosystems of the Northwest Atlantic that occurred during the early 1990s. This regime shift resulted from freshening and stratification of the shelf waters, which in turn could be linked to changes in the abundances and seasonal cycles of phytoplankton, zooplankton, and higher trophic-level consumer populations. It is predicted that the recently observed ecological responses to Arctic climate change in the North Atlantic will continue into the near future if current trends in sea ice, freshwater export, and surface ocean salinity continue. It is more difficult to predict ecological responses to abrupt climate change in the more distant future as tipping points in the Earth's climate system are exceeded.

Ecology↗

Hierarchical spatiotemporal matrix models for characterizing invasions

The growth and dispersal of biotic organisms is an important subject in ecology. Ecologists are able to accurately describe survival and fecundity in plant and animal populations and have developed quantitative approaches to study the dynamics of dispersal and population size. Of particular interest are the dynamics of invasive species. Such nonindigenous animals and plants can levy significant impacts on native biotic communities. Effective models for relative abundance have been developed; however, a better understanding of the dynamics of actual population size (as opposed to relative abundance) in an invasion would be beneficial to all branches of ecology. In this article, we adopt a hierarchical Bayesian framework for modeling the invasion of such species while addressing the discrete nature of the data and uncertainty associated with the probability of detection. The nonlinear dynamics between discrete time points are intuitively modeled through an embedded deterministic population model with density-dependent growth and dispersal components. Additionally, we illustrate the importance of accommodating spatially varying dispersal rates. The method is applied to the specific case of the Eurasian Collared-Dove, an invasive species at mid-invasion in the United States at the time of this writing. ?? 2006, The International Biometric Society.

Biometrics↗

Ecological correlates of invasion impact for Burmese pythons in Florida

An invasive population of Burmese pythons ( Python molurus bivittatus ) is established across several thousand square kilometers of southern Florida and appears to have caused precipitous population declines among several species of native mammals. Why has this giant snake had such great success as an invasive species when many established reptiles have failed to spread? We scored the Burmese python for each of 15 literature-based attributes relative to predefined comparison groups from a diverse range of taxa and provide a review of the natural history and ecology of Burmese pythons relevant to each attribute. We focused on attributes linked to spread and magnitude of impacts rather than establishment success. Our results suggest that attributes related to body size and generalism appeared to be particularly applicable to the Burmese python's success in Florida. The attributes with the highest scores were: high reproductive potential, low vulnerability to predation, large adult body size, large offspring size and high dietary breadth. However, attributes of ectotherms in general and pythons in particular (including predatory mode, energetic efficiency and social interactions) might have also contributed to invasion success. Although establishment risk assessments are an important initial step in prevention of new establishments, evaluating species in terms of their potential for spreading widely and negatively impacting ecosystems might become part of the means by which resource managers prioritize control efforts in environments with large numbers of introduced species.

Florida↗

Temporal variation in survival and recovery rates of lesser scaup: A response

We recently analyzed long-term (1951–2011) continental band-recovery data from lesser scaup ( Aythya affinis ) and demonstrated that harvest rates declined through time, but annual survival rates exhibited no such trends; moreover, annual harvest and survival rates were uncorrelated for all age-sex classes. We therefore concluded that declining fecundity was most likely responsible for recent population declines, rather than changes in harvest or survival. Lindberg et al. ( 2017 ) critiqued our conclusions, arguing that we did little more than fail to reject a null hypothesis of compensatory mortality, postulated ecologically unrealistic changes in fecundity, and failed to give sufficient consideration to additive harvest mortality. Herein, we re-summarize our original evidence indicating that harvest has been compensatory, or at most weakly additive, and demonstrate that our analysis had sufficient power to detect strongly additive mortality if it occurred. We further demonstrate that our conclusions were not confounded by population size, band loss, or individual heterogeneity, as suggested by Lindberg et al. ( 2017 ), and we provide additional support for our conjecture that low fecundity played a major role in declining scaup populations during 1983–2006. We therefore reiterate our original management recommendations: given low harvest rates and lack of demonstrable effect on scaup survival, harvest regulations could return to more liberal frameworks, and waterfowl biologists should work together to continue banding lesser scaup and use these data to explore alternative hypotheses to identify the true ecological causes of population change, given that it is unlikely to be excessive harvest.

Journal of Wildlife Management↗

Golden Eagle Monitoring Plan for the Desert Renewable Energy Conservation Plan

This report describes options for monitoring the status and population trends of the golden eagle (Aquila chrysaetos) within the Desert Renewable Energy Conservation Plan (DRECP) area of Southern California in maintaining stable or increasing population in the planning area. The report profiles the ecology of golden eagles in the region and provides a range of potential sampling options to address monitoring needs and objectives. This approach also focused on links between changes in human land-use, golden eagle nesting and foraging habitat conditions, and population dynamics. The report outlines how monitoring data from demographic, prey, and habitat studies were used to develop a predictive demographic model for golden eagles in the DRECP area. Results from the model simulations suggest increases in renewable energy development could have negative consequences for population trajectories. Results also suggest site-specific conservation actions could reduce the magnitude of negative impacts to the local population of eagles. A monitoring framework is proposed including: (1) annual assessments of site-occupancy and reproduction by territorial pairs of golden eagles (including rates at which sites become colonized or vacated over time); (2) estimates of survival, movements, and intensity of use of landscapes by breeding and non-breeding golden eagles; (3) periodic (conducted every two to four years) assessments of nesting and foraging habitats, prey populations, and associations with land-use and management activities; and (4) updating the predictive demographic model with new information obtained on eagles and associated population stressors. The results of this research were published in the Journal of Rapture Research, Wiens, David,Inman, Rich D., Esque, Todd C., Longshore, Kathleen M. and Nussear, Kenneth (2017). Spatial Demographic Models to Inform Conservation Planning of Golden Eagles in Renewable Energy Landscapes. 51(3):234-257.

Report↗

Molecular detection of hematozoa infections in tundra swans relative to migration patterns and ecological conditions at breeding grounds

Tundra swans ( Cygnus columbianus ) are broadly distributed in North America, use a wide variety of habitats, and exhibit diverse migration strategies. We investigated patterns of hematozoa infection in three populations of tundra swans that breed in Alaska using satellite tracking to infer host movement and molecular techniques to assess the prevalence and genetic diversity of parasites. We evaluated whether migratory patterns and environmental conditions at breeding areas explain the prevalence of blood parasites in migratory birds by contrasting the fit of competing models formulated in an occupancy modeling framework and calculating the detection probability of the top model using Akaike Information Criterion (AIC). We described genetic diversity of blood parasites in each population of swans by calculating the number of unique parasite haplotypes observed. Blood parasite infection was significantly different between populations of Alaska tundra swans, with the highest estimated prevalence occurring among birds occupying breeding areas with lower mean daily wind speeds and higher daily summer temperatures. Models including covariates of wind speed and temperature during summer months at breeding grounds better predicted hematozoa prevalence than those that included annual migration distance or duration. Genetic diversity of blood parasites in populations of tundra swans appeared to be relative to hematozoa prevalence. Our results suggest ecological conditions at breeding grounds may explain differences of hematozoa infection among populations of tundra swans that breed in Alaska.

Alaska↗

Reproductive ecology of the green treefrog (Hyla cinerea) in Northwestern Florida

Information on life-history traits is critical to understanding population dynamics of anurans. The objective of this study was to examine aspects of the reproductive ecology of Hyla cinerea in northwestern Florida. Four breeding localities in Leon County, Florida, were sampled over three seasons (2001-2003), amplexed pairs were found as early as 12 April and as late as 12 August. Egg clutches were counted from 51 amplexed pairs and adult size was measured in 43 pairs. Average clutch size was 1214 ?? 528 eggs (x- ?? SE, range = 359-2658). Female H. cinerea were slightly larger than males (x- ?? SE tibiofibula length = 24.9 ?? 2.2 and 24 ?? 1.7 mm, respectively). Female size was significantly positively correlated with clutch size and weakly correlated with size of the paired male. Comparison of the results of this study with previous research indicates that the reproductive ecology of H. cinerea varies across its geographic range.

American Midland Naturalist↗

To catch a (marsh) predator: Modified trapping methods for breeding and wintering Northern Harriers (Circus hudsonius)

Although there are a variety of methods available for trapping raptors, some species, such as Northern Harriers ( Circus hudsonius ), are not easily captured with standard methods. We tested several existing trapping methods and modified two of them based on Northern Harrier ecology and behavior across seasons in a study population in California. No previously successful methods described in the literature were effective for our study population. Two modified methods were most effective for trapping Northern Harriers: (1) placing two dho-gazas around the nest in a V-shape and flushing the adult female into the nets during the breeding season, and (2) using remote-triggered bow nets baited with waterbird carcasses in winter. Dho-gazas at the nest worked well during the early nestling-rearing stage, when nestlings were younger than 2 wk old and adult females were most attentive. This method was not suitable during the incubation stage because Northern Harriers are prone to nest abandonment. In the winter, Northern Harriers are known to scavenge, yet this aspect of their behavioral ecology has previously been rarely exploited for trapping purposes. These two methods allow for selective Northern Harrier trapping across seasons and provide modified options for research on this understudied and declining species in North America.

California↗

Anthropogenic subsidies influence resource use during a mange epizootic in a desert coyote population

Colonization of urban areas by synanthropic wildlife introduces novel and complex alterations to established ecological processes, including the emergence and spread of infectious diseases. Aggregation at urban resources can increase disease transfer, with wide-ranging species potentially infecting outlying populations. The garrison at the National Training Center, Fort Irwin, California, USA, was recently colonized by mange-infected coyotes ( Canis latrans ) that also use the surrounding Mojave Desert. This situation provided an ideal opportunity to examine the effects of urban resources on disease dynamics. We evaluated seasonal space use and determined the influence of anthropogenic subsidies, water sources, and prey density on urban resource selection. We found no difference in home range size between healthy and infected individuals, but infected residents had considerably more spatial overlap with one another than healthy residents. All coyotes selected for anthropogenic subsidies during all seasons, while infected coyotes seasonally selected for urban water sources, and healthy coyotes seasonally selected for urban areas with greater densities of natural prey. These results suggest that while all coyotes were selecting for anthropogenic subsidies, infected resident coyotes demonstrated a greater tolerance for other conspecifics, which could be facilitating the horizontal transfer of sarcoptic mange to non-resident coyotes. Conversely, healthy coyotes also selected for natural prey and healthy residents exhibited a lack of spatial overlap with other coyotes suggesting they were not reliant on anthropogenic subsidies and were maintaining territories. Understanding the association between urban wildlife, zoonotic diseases, and urban resources can be critical in determining effective responses for mitigating future epizootics.

California↗

Population trends in Vermivora warblers are linked to strong migratory connectivity

Migratory species can experience limiting factors at different locations and during different periods of their annual cycle. In migratory birds, these factors may even occur in different hemispheres. Therefore, identifying the distribution of populations throughout their annual cycle (i.e., migratory connectivity) can reveal the complex ecological and evolutionary relationships that link species and ecosystems across the globe and illuminate where and how limiting factors influence population trends. A growing body of literature continues to identify species that exhibit weak connectivity wherein individuals from distinct breeding areas co-occur during the nonbreeding period. A detailed account of a broadly distributed species exhibiting strong migratory connectivity in which nonbreeding isolation of populations is associated with differential population trends remains undescribed. Here, we present a range-wide assessment of the nonbreeding distribution and migratory connectivity of two broadly dispersed Nearctic-Neotropical migratory songbirds. We used geolocators to track the movements of 70 Vermivora warblers from sites spanning their breeding distribution in eastern North America and identified links between breeding populations and nonbreeding areas. Unlike blue-winged warblers ( Vermivora cyanoptera ), breeding populations of golden-winged warblers ( Vermivora chrysoptera ) exhibited strong migratory connectivity, which was associated with historical trends in breeding populations: stable for populations that winter in Central America and declining for those that winter in northern South America.

Proceedings of the National Academy of Sciences of↗

Seasonal components of avian population change: Joint analysis of two large-scale monitoring programs

We present a combined analysis of data from two large-scale surveys of bird populations. The North American Breeding Bird Survey is conducted each summer; the Christmas Bird Count is conducted in early winter. The temporal staggering of these surveys allows investigation of seasonal components of population change, which we illustrate with an examination of the effects of severe winters on the Carolina Wren ( Thryothorus ludovicianus ). Our analysis uses a hierarchical log-linear model with controls for survey-specific sampling covariates. Temporal change in population size is modeled seasonally, with covariates for winter severity. Overall, the winter-spring seasons are associated with 82% of the total population variation for Carolina Wrens, and an additional day of snow cover during winter-spring is associated with an incremental decline of 1.1% of the population.

Ecology↗

Distribution of microbial physiologic types in an aquifer contaminated by crude oil

We conducted a plume-scale study of the microbial ecology in the anaerobic portion of an aquifer contaminated by crude-oil compounds. The data provide insight into the patterns of ecological succession, microbial nutrient demands, and the relative importance of free-living versus attached microbial populations. The most probable number (MPN) method was used to characterize the spatial distribution of six physiologic types: aerobes, denitrifiers, iron-reducers, heterotrophic fermenters, sulfate-reducers, and methanogens. Both free-living and attached numbers were determined over a broad cross-section of the aquifer extending horizontally from the source of the plume at a nonaqueous oil body to 66 m downgradient, and vertically from above the water table to the base of the plume below the water table. Point samples from widely spaced locations were combined with three closely spaced vertical profiles to create a map of physiologic zones for a cross-section of the plume. Although some estimates suggest that less than 1% of the subsurface microbial population can be grown in laboratory cultures, the MPN results presented here provide a comprehensive qualitative picture of the microbial ecology at the plume scale. Areas in the plume that are evolving from iron-reducing to methanogenic conditions are clearly delineated and generally occupy 25-50% of the plume thickness. Lower microbial numbers below the water table compared to the unsaturated zone suggest that nutrient limitations may be important in limiting growth in the saturated zone. Finally, the data indicate that an average of 15% of the total population is suspended.

Microbial Ecology↗