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James S. Sedinger

Publications and source records attributed to James S. Sedinger.

At least 19 recordsLinked to original sources

Interacting sea-level rise, sea-ice loss, storm flooding, erosion, and permafrost thaw threaten ecosystems, wildlife, and communities on the Yukon-Kuskokwim Delta

The Yukon-Kuskokwim Delta has the largest intertidal wetland in North America, is a globally critical breeding area for waterbirds, and is home to the largest regional indigenous population in the Arctic. Here, coastal tundra ecosystems, wildlife, and indigenous communities are highly vulnerable to sea-ice loss in the Bering Sea, sea-level rise, storm flooding, erosion, and collapsing ground from permafrost thaw caused by climate warming. These drivers interact in non-linear ways to increase flooding, salinization, and sedimentation, and thus, alter ecosystem trajectories and broader landscape evolution. Rapid changes in these factors over decadal time scales are highly likely to cause transformative shifts in coastal ecosystems across roughly 70% of the outer delta this century. We project saline and brackish ecotypes on the active delta floodplain with frequent sedimentation will maintain dynamic equilibrium with sea-level rise and flooding, slightly brackish ecotypes on the inactive floodplain with infrequent flooding and low sedimentation rates will be vulnerable to increased flooding and likely transition to more saline and brackish ecotypes, and fresh lacustrine and lowland ecotypes on the abandoned floodplain with permafrost plateaus will be vulnerable to thermokarst, salinization and flooding that will shift them toward brackish ecosystems. This will greatly affect bird nesting and foraging habitats, with both winners and losers. Already, some Yup'ik communities are facing relocation of their low-lying villages. The societal challenges and consequences of adapting to these changing landscapes are enormous and will require a huge societal effort.

Alaska

Greater sage-grouse seasonal habitat associations: A review and considerations for interpretation and management applications

Habitat features needed by wildlife can change in composition throughout the year, particularly in temperate ecosystems, leading to distinct seasonal spatial-use patterns. Studies of species-habitat associations therefore often focus on understanding relationships within discrete seasonal periods with common goals of prediction (e.g., habitat mapping) and inference (e.g., interpreting model coefficients). Across the range of the greater sage-grouse ( Centrocercus urophasianus ) of western North America, the increasing use of high-frequency tracking devices has led to a surge in habitat association studies covering multiple temporal periods and spatial extents. We reviewed the literature for seasonal habitat association studies corresponding to the second and third orders of selection (Johnson 1980). Our objectives were to summarize the methodological approaches used to estimate habitat associations to aid understanding in cross-study comparisons and identify common habitat features reported as selected or avoided within different seasonal periods. We reviewed 71 second- and third-order studies published from 2007–2023 that evaluated covariates collected in a geographic information system (GIS) and modeled probability of selection or intensity of use. The most common study design evaluated a single level of selection (third-order) and was multi-scale (i.e., covariates were measured at varying spatial grains). The most common model approach estimated habitat associations using resource selection functions (RSFs) fit with logistic regression. Studies mostly focused on the breeding periods and winter, but all seasons throughout the annual cycle were covered. There was clear support for selection of sagebrush and avoidance of trees and rugged terrain across seasons, and strong selection of mesic conditions in summer. However, habitat associations for most covariates were mixed, with proportionally equivalent selection and avoidance reported, even within the same seasons. Different factors hampered cross-study comparisons, including variation in study design, but additional contributors likely included important context-dependent habitat associations, such as functional responses to changing habitat availability. We suggest collaborative studies leveraging multiple datasets can help improve seasonal habitat inference by removing the effects of variable study designs.

Journal of Wildlife Management

Shortening migration by 4500 km does not affect nesting phenology or increase nest success for black brant (Branta bernicla nigricans) breeding in Arctic and subarctic Alaska

Background Since the 1980s, Pacific Black Brant ( Branta bernicla nigricans , hereafter brant) have shifted their winter distribution northward from Mexico to Alaska (approximately 4500 km) with changes in climate. Alongside this shift, the primary breeding population of brant has declined. To understand the population-level implications of the changing migration strategy of brant, it is important to connect movement and demographic data. Our objectives were to calculate migratory connectivity, a measure of spatial and temporal overlap during the non-breeding period, for Arctic and subarctic breeding populations of brant, and to determine if variation in migration strategies affected nesting phenology and nest survival. Methods We derived a migratory network using light-level geolocator migration tracks from an Arctic site (Colville River Delta) and a subarctic site (Tutakoke River) in Alaska. Using this network, we quantified the migratory connectivity of the two populations during the winter. We also compared nest success rates among brant that used different combinations of winter sites and breeding sites. Results The two breeding populations were well mixed during the winter, as indicated by a migratory connectivity score close to 0 (− 0.06) at the primary wintering sites of Izembek Lagoon, Alaska (n = 11 brant) and Baja California, Mexico (n = 48). However, Arctic birds were more likely to migrate the shorter distance to Izembek (transition probability = 0.24) compared to subarctic birds (transition probability = 0.09). Nest survival for both breeding populations was relatively high (0.88–0.92), and we did not detect an effect of wintering site on nest success the following year. Conclusions Nest survival of brant did not differ among brant that used wintering sites despite a 4500 km difference in migration distances. Our results also suggested that the growing Arctic breeding population is unlikely to compensate for declines in the larger breeding population of brant in the subarctic. However, this study took place in 2011–2014 and wintering at Izembek Lagoon may have greater implications for reproductive success under future climate conditions.

Movement Ecology

Mate fidelity improves survival and breeding propensity of a long‐lived bird

Evolutionary and behavioural ecologists have long been interested in factors shaping the variation in mating behaviour observed in nature. Although much of the research on this topic has focused on the consequences of mate choice and mate change on annual reproductive success, studies of a potential positive link between mate fidelity and adult demographic rates have been comparatively rare. This is particularly true for long‐lived birds with multi‐year, socially monogamous pair bonds. We used a 26‐year capture–mark–recapture dataset of 3,330 black brent Branta bernicla nigricans to test whether breeding with a familiar mate improved future breeding propensity and survival. We predicted that experienced breeders nesting with a new partner would have rates of survival similar to familiar pairs because long‐lived species avoid jeopardizing survival since their lifetime fitness is sensitive to this vital rate. In contrast, we expected that any costs of breeding with a new partner would be paid through skipping the subsequent breeding attempt. We found that unfamiliar pairs had lower subsequent breeding propensity than faithful partners. However, contrary to our expectations, individuals breeding with a new mate also suffered reduced survival. These results add to a small number of studies indicating that a positive relationship between mate retention and adult demographic rates may exist in a diverse array of avian species. Given these results, researchers should consider costs of mate change that extend beyond within‐season reproductive success to fully understand the potential adaptive basis for perennial social monogamy. We caution that if mate retention enhances survival prospects, improvements in annual reproductive success with pair‐bond length could be a secondary factor favouring perennial social monogamy, particularly in species with slower life‐history strategies. Furthermore, some cases where annual reproductive success does not improve with pair‐bond duration, yet multi‐year pair bonds are common, could be explained by benefits afforded by mate fidelity to adult vital rates.

Journal of Animal Ecology

Geese mediate vegetation state changes with parallel effects on N cycling that leave nutritional legacies for offspring

Along the coastal fringe of the Yukon–Kuskokwim River Delta in southwestern Alaska, geese maintain grazing lawns dominated by a rhizomatous sedge that, when ungrazed, transitions to a taller, less palatable growth form that is taxonomically described as a different species. Nutrients recycled in goose feces, in conjunction with grazing, are critical to the rapid, nutritious growth of grazing lawns, and selective foraging on lawns has positive life‐history consequences for goslings. To examine whether bidirectional vegetation shifts were accompanied by parallel changes in N cycling, we studied how 15 N‐urea and 13 C 15 N‐glycine were processed through soils and plants of native and recently reverted vegetation states. Biomass and plant 15 N uptake from plots reverted to the tall growth form using exclosures and from those shifted to grazing lawns by experimental clipping and then goose grazing were identical to their native counterparts. Total recovery of 15 N within the tall vegetation types was significantly greater than within grazing lawns, although when expressed on a per‐gram biomass basis, percentage of 15 N recovery was significantly higher in grazing lawns compared with the tall vegetation state. Patterns of 13 C enrichment in CO 2 soil efflux showed rapid use of 13 C‐glycine as a respiratory substrate within the first hour following injection, with both the timing and magnitude of efflux occurring at similar time points for all four vegetation types. However, higher soil respiration rates and a shorter half‐life for 13 C‐glycine in soils from tall meadows resulted in a greater proportional loss of 13 CO 2 compared with grazing lawns. Despite daily‐to‐weekly tidal inundation, all of 15 N from labeled substrates could be accounted for within 1 m of the injection grid from soils of both states after 30 d, with significant levels of 15 N in soils and vegetation after one year. Geese have remarkably high fidelity to brood‐rearing areas, returning as adults to the same grazing lawns where they were raised as goslings. Our data suggest that the role fecal‐derived nutrients play in the positive feedback loop between geese and their food resources can provide a long‐term legacy that spans generations.

Alaska

Ecosystem scale loss of grazing habitat impacted by abundance of dominant herbivores

Grazing lawns, patches of grazing tolerant plants with high nutrient value, provide important habitat for herbivores, and changes in abundance can impact herbivore populations. Grazing lawns are maintained in quality and quantity by repeated grazing and are a result of a positive feedback since the availability of grazing lawn can increase herbivore populations and increased herbivore populations can result in an increase in grazing lawn extent. We sampled aerial imagery from a long-term dataset (>20 yrs) at an internationally important breeding area for avian herbivores to model changes in grazing lawn abundance over time and identify the possible factors impacting those changes, including numbers of breeding birds, their primary predator, and spring phenology. Our data suggests that avian herbivores and their predators likely exert strong impacts on plant communities and may drive vegetation abundance. Decreases in the number of herbivore nests in our study coincided with an almost complete lack of grazing lawn in the mid-2000s. Any factors dictating the amount of grazing lawn available for avian herbivores could strongly influence breeding success and the maximum size of these populations. Our results demonstrate the importance of studying complex interactions among predators, herbivores and plants, and population moderation by both bottom-up and top-down processes.

Ecosphere

Changes in behavior are unable to disrupt a trophic cascade involving a specialist herbivore and its food plant

Changes in ecological conditions can induce changes in behavior and demography of wild organisms, which in turn may influence population dynamics. Pacific black brant (Branta bernicla nigricans) nesting in colonies on the Yukon-Kuskokwim Delta (YKD) in western Alaska have declined substantially (~50%) since the turn of the century. Pacific black brant are herbivores that rely heavily on Carex subspathacea (Hoppner’s sedge) during growth and development. The availability of C. subspathacea affects gosling growth rates, which subsequently affect pre- and post-fledging survival, as well as size and breeding probability as an adult. We predicted that long-term declines in C. subspathacea have affected gosling growth rates, despite the potential of behavior to buffer changes in food availability during brood rearing. We used Bayesian hierarchical mixed-effects models to examine long-term (1987 – 2015) shifts in brant behavior during brood-rearing, forage availability, and gosling growth rates at the Tutakoke River colony. We showed that locomotion behaviors have increased (β = 0.05, 95% CRI 0.032 – 0.068) while resting behaviors have decreased (β = -0.024, 95% CRI -0.041 – -0.007), potentially in response to long-term shifts in forage availability and brood density. Concurrently, gosling growth rates have decreased substantially (β = -0.096, 95% CRI -0.198 – -0.014) despite shifts in behavior, mirroring long-term declines in the abundance of C. subspathacea (β = -0.194, 95% CRI -0.350 – -0.037). These results have important implications for individual fitness and population viability, where shifts in gosling behavior putatively fail to mitigate long-term declines in forage availability.

Article

The black brant population is declining based on mark recapture

Annual survival and recruitment in black brant ( Branta bernicla nigricans ) have declined since the 1990s, yet aerial surveys of the global population have been stable or even increasing over the past decade. We used a combination of a Lincoln estimator based on harvest information and band recoveries, and marked‐unmarked ratios in bag checks in 1 harvest area in Mexico to estimate the number of adults in the population during 1992–2015. We produced weighted means from the 2 kinds of estimates for years in which we had data for both, with weights equal to the inverse of the variance of the individual estimates. We treated the black brant population as consisting of 2 subpopulations. One population consisted of breeding black brant on the Yukon‐Kuskokwim Delta (YKD), Alaska, USA, and the other consisted of Arctic (northern Alaska, western Canada, and eastern Russia) breeders, and nonbreeders and failed breeders from the YKD that underwent molt migration to the Arctic. For the global population estimates, we assessed potential bias due to differential marking and harvest of the 2 subpopulations, which was approximately 1%, probably because band recovery rates were similar for the 2 subpopulations. Population estimates declined from 229,980 (average for 1999–2002) to 161,504 (average for 2012–2015). Population estimates based on estimated harvest were variable but more stable in the later years of the study, when larger numbers of brant hunters were included in the sample. We suggest that the combination of Lincoln estimates and bag check data provides a reasonable and cost effective approach to monitoring the population.

Journal of Wildlife Management

Spatial distribution of band recoveries of black brant

On average, band recovery rates of adult black brant ( Branta bernicla nigricans ) more than doubled between the 2000s and 2010s. However, the spatial distribution of band recoveries of black brant has not been reported. Our objective was to describe the spatial distribution of band recoveries of black brant since 1990. We found that Alaska, California, and Mexico accounted for ≥89% of band recoveries for black brant released from the Arctic and the Tutakoke River Colony in southwestern Alaska, in each decade studied. Although recovery rates increased in each major harvest region from the 1990s to 2010s, increases were not even. For brant released from the Arctic, the recovery rate in Alaska has gone up 7‐fold, whereas the recovery rate in Mexico has increased 1.3‐fold since the 1990s. For brant banded in the Arctic, the increased recovery rates in Alaska resulted largely from a rise in recoveries from the Izembek Lagoon area. For brant banded at the Tutakoke River Colony, the recovery rate in Alaska increased 4.8‐fold, whereas recovery rates in Mexico increased 1.6‐fold. Despite the reduced relative contribution of Mexico to band recoveries in the 2010s, Bahia San Quintin, Mexico, still contributes more recoveries than any other wintering estuary. Because 57–60% of black brant band recoveries occur at the localities of Izembek Lagoon, Alaska; Humboldt Bay, California; and Bahia San Quintin, it is likely that accurate annual estimates of the black brant population using Lincoln's method could be derived from hunter bag checks at these 3 areas. If population managers are interested in managing harvest rates of black brant, they could focus efforts on the main hunting areas we highlight in this paper. Finally, it is unclear if the recent increases in band recovery rates are the result of increased harvest, a declining population, or both; therefore, we suggest refinement of population monitoring programs and continued monitoring of band recovery rates.

Journal of Wildlife Management

The migratory bird treaty and a century of waterfowl conservation

In the final decades of the nineteenth century, concern was building about the status of migratory bird populations in North America. In this literature review, we describe how that concern led to a landmark conservation agreement in 1916, between the United States and Great Britain (on behalf of Canada) to conserve migratory birds shared by Canada and the United States. Drawing on published literature and our personal experience, we describe how subsequent enabling acts in both countries gave rise to efforts to better estimate population sizes and distributions, assess harvest rates and demographic impacts, design and fund landscape-level habitat conservation initiatives, and organize necessary political and regulatory processes. Executing these steps required large-scale thinking, unprecedented regional and international cooperation, ingenuity, and a commitment to scientific rigor and adaptive management. We applaud the conservation efforts begun 100 years ago with the Migratory Bird Treaty Convention. The agreement helped build the field of wildlife ecology and conservation in the twentieth century but only partially prepares us for the ecological and social challenges ahead.

Journal of Wildlife Management

Declining survival of black brant from subarctic and arctic breeding areas

Since the mid 1990s, the number of black brant ( Branta bernicla nigricans ; brant) nests on the Yukon‐Kuskokwim Delta (YKD), Alaska, USA, the historically predominant breeding area of brant, has declined steadily. This has caused researchers and managers to question if arctic breeding populations can compensate for the reduction in brant nests on the YKD. An important component of the assessment of brant population dynamics is having current estimates of first‐year and adult survival. We banded brant at 4 locations in Arctic Alaska and western Canada, and at 1 location in the subarctic, the Tutakoke River (TR) colony on the YKD, 1990–2015. We used joint live and dead mark‐recapture models to estimate first‐year and adult (≥1 yr old) survival of brant. We also used band recovery rates from a Brownie model to assess temporal trends in band recovery rates of adult brant. First‐year survival of brant hatched at TR declined from approximately 0.60 to <0.20 and, although first‐year survival generally was higher for goslings marked in the Arctic, their survival declined from approximately 0.70 in the early 1990s to ≤0.45 in the 2010s. Annual survival of adult females decreased from an average of 0.881 (95% CI = 0.877–0.885) to 0.822 (95% CI = 0.815–0.829) at TR and from 0.851 (95% CI = 0.843–0.860) to 0.821 (95% CI = 0.805–0.836) in the Arctic, from 1990 to 2014. Band recovery rates of adults generally were <1.25% until the last several years of study, when they reached ≤3.5%. Although the current harvest rates may be partially additive to natural mortality, we do not believe that harvest is the main influence on the declines in survival. The general decline in survival rates of brant breeding across a large geographic area may be influenced by a reduction in the quality of migration and wintering ground habitats. We suggest an analysis of seasonal survival of brant to test the hypothesis that declining habitat quality on wintering or spring migration areas is reducing survival. Our results suggest that the number of breeding pairs at TR will continue to decline and also brings into question the ability of arctic breeding populations to grow at a rate necessary to offset the declines on the YKD. Researchers should continue to closely monitor survival and harvest rates of brant, and assess methods currently used to monitor their abundance.

Journal of Wildlife Management

Growth of black brant and lesser snow goose goslings in northern Alaska

Gosling body mass can affect first year survival, recruitment, adult body size, and future fecundity of geese, and can serve as an indicator of forage availability and quality on brood-rearing areas. From 2012–2014 we measured body mass of 76 black brant ( Branta bernicla nigricans ) and 268 lesser snow goose ( Chen caerulescens caerulescens ) goslings of known age on the Colville River Delta (CRD) of northern Alaska to determine if there was evidence of density-dependent declines in gosling growth following recent population increases of those species and sympatric greater white-fronted geese ( Anser albifrons frontalis ). We contrasted contemporary body mass of brant goslings and forage biomass in brood-rearing habitats that were shared by all species, with measures obtained on, and near the CRD in the 1990s, prior to the establishment of snow goose nesting colonies in the area. Body mass of brant goslings recaptured between 25 and 32 days of age had not changed over the past 2 decades, despite an influx of snow geese, and increases in populations of brant and white-fronted geese. At 30 days of age, body mass of brant goslings on the CRD was 100–400 g heavier than for brant goslings of the same age on the Yukon-Kuskokwim Delta (YKD), Alaska. Contemporary biomass of grazed Carex subspathacea on CRD brood-rearing areas was comparable to the 1990s and was 2–4 times greater than for the same plant community on the YKD. Historical data on growth of snow goose goslings were not available for the CRD. However, average body mass of 34-day-old snow goose goslings was > 230 g heavier than for conspecifics of the same age in the Hudson Bay region. We conclude that the establishment of nesting snow geese on the CRD has not negatively affected brant gosling growth, and that recent population increases of all species have likely not been constrained by forage availability on brood-rearing areas. Barring demographic changes elsewhere in their annual cycles, we predict that goose populations will continue to increase in northern Alaska. However, snow geese are increasing more rapidly than brant in the region. Because the black brant population has periodically been below conservation objectives, the effects of the increasing number of snow geese on forage biomass and growth of brant goslings in northern Alaska should be monitored.

Alaska

Carryover effects and climatic conditions influence the postfledging survival of greater sage-grouse

Prebreeding survival is an important life history component that affects both parental fitness and population persistence. In birds, prebreeding can be separated into pre- and postfledging periods; carryover effects from the prefledging period may influence postfledging survival. We investigated effects of body condition at fledging, and climatic variation, on postfledging survival of radio-marked greater sage-grouse ( Centrocercus urophasianus ) in the Great Basin Desert of the western United States. We hypothesized that body condition would influence postfledging survival as a carryover effect from the prefledging period, and we predicted that climatic variation may mediate this carryover effect or, alternatively, would act directly on survival during the postfledging period. Individual body condition had a strong positive effect on postfledging survival of juvenile females, suggesting carryover effects from the prefledging period. Females in the upper 25th percentile of body condition scores had a postfledging survival probability more than twice that (&Phi; = 0.51 &plusmn; 0.06 SE) of females in the bottom 25th percentile (&Phi; = 0.21 &plusmn; 0.05 SE). A similar effect could not be detected for males. We also found evidence for temperature and precipitation effects on monthly survival rates of both sexes. After controlling for site-level variation, postfledging survival was nearly twice as great following the coolest and wettest growing season (&Phi; = 0.77 &plusmn; 0.05 SE) compared with the hottest and driest growing season (&Phi; = 0.39 &plusmn; 0.05 SE). We found no relationships between individual body condition and temperature or precipitation, suggesting that carryover effects operated independently of background climatic variation. The temperature and precipitation effects we observed likely produced a direct effect on mortality risk during the postfledging period. Conservation actions that focus on improving prefledging habitat for sage-grouse may have indirect benefits to survival during postfledging, due to carryover effects between the two life phases.

Ecology and Evolution

A likelihood-based approach for assessment of extra-pair paternity and conspecific brood parasitism in natural populations

Genotypes are frequently used to assess alternative reproductive strategies such as extra-pair paternity and conspecific brood parasitism in wild populations. However, such analyses are vulnerable to genotyping error or molecular artifacts that can bias results. For example, when using multilocus microsatellite data, a mismatch at a single locus, suggesting the offspring was not directly related to its putative parents, can occur quite commonly even when the offspring is truly related. Some recent studies have advocated an ad-hoc rule that offspring must differ at more than one locus in order to conclude that they are not directly related. While this reduces the frequency with which true offspring are identified as not directly related young, it also introduces bias in the opposite direction, wherein not directly related young are categorized as true offspring. More importantly, it ignores the additional information on allele frequencies which would reduce overall bias. In this study, we present a novel technique for assessing extra-pair paternity and conspecific brood parasitism using a likelihood-based approach in a new version of program cervus. We test the suitability of the technique by applying it to a simulated data set and then present an example to demonstrate its influence on the estimation of alternative reproductive strategies.

Molecular Ecology Resources

Evidence that life history characteristics of wild birds influence infection rates and exposure to influenza A viruses

We report on life history characteristics, temporal, and age-related effects influencing the frequency of occurrence of avian influenza (AI) viruses in four species of migratory geese breeding on the Yukon-Kuskokwim Delta, Alaska. Emperor geese ( Chen canagica ), cackling geese ( Branta hutchinsii ), greater white-fronted geese ( Anser albifrons ), and black brant ( Branta bernicla ), were all tested for active infection of AI viruses upon arrival in early May, during nesting in June, and while molting in July and August, 2006–2010 ( n = 14,323). Additionally, prior exposure to AI viruses was assessed via prevalence of antibodies from sera samples collected during late summer in 2009 and 2010. Results suggest that geese are uncommonly infected by low pathogenic AI viruses while in Alaska. The percent of birds actively shedding AI viruses varied annually, and was highest in 2006 and 2010 (1–3%) and lowest in 2007, 2008, and 2009 (<0.70%). Contrary to findings in ducks, the highest incidence of infected birds was in late spring when birds first arrived from staging and wintering areas. Despite low prevalence, most geese were previously exposed to AI viruses, as indicated by high levels of seroprevalence during late summer (47%–96% across species; n = 541 ). Seroprevalence was >95% for emperor geese, a species that spends part of its life cycle in Asia and is endemic to Alaska and the Bering Sea region, compared to 40–60% for the other three species, whose entire life cycles are within the western hemisphere. Birds <45 days of age showed little past exposure to AI viruses, although antibodies were detected in samples from 5-week old birds in 2009. Seroprevalence of known age black brant revealed that no birds <4 years old had seroconverted, compared to 49% of birds ≥4 years of age.

Alaska

Intraseasonal variation in survival and probable causes of mortality in greater sage-grouse Centrocercus urophasianus

The mortality process is a key component of avian population dynamics, and understanding factors that affect mortality is central to grouse conservation. Populations of greater sage-grouse Centrocercus urophasianus have declined across their range in western North America. We studied cause-specific mortality of radio-marked sage-grouse in Eureka County, Nevada, USA, during two seasons, nesting (2008-2012) and fall (2008-2010), when survival was known to be lower compared to other times of the year. We used known-fate and cumulative incidence function models to estimate weekly survival rates and cumulative risk of cause-specific mortalities, respectively. These methods allowed us to account for temporal variation in sample size and staggered entry of marked individuals into the sample to obtain robust estimates of survival and cause-specific mortality. We monitored 376 individual sage-grouse during the course of our study, and investigated 87 deaths. Predation was the major source of mortality, and accounted for 90% of all mortalities during our study. During the nesting season (1 April - 31 May), the cumulative risk of predation by raptors (0.10; 95% CI: 0.05-0.16) and mammals (0.08; 95% CI: 0.03-013) was relatively equal. In the fall (15 August - 31 October), the cumulative risk of mammal predation was greater (M (mam) = 0.12; 95% CI: 0.04-0.19) than either predation by raptors (M (rap) = 0.05; 95% CI: 0.00-0.10) or hunting harvest (M (hunt) = 0.02; 95% CI: 0.0-0.06). During both seasons, we observed relatively few additional sources of mortality (e.g. collision) and observed no evidence of disease-related mortality (e.g. West Nile Virus). In general, we found little evidence for intraseasonal temporal variation in survival, suggesting that the nesting and fall seasons represent biologically meaningful time intervals with respect to sage-grouse survival.

Nevada

Harvest and dynamics of duck populations

The role of harvest in the dynamics of waterfowl populations continues to be debated among scientists and managers. Our perception is that interested members of the public and some managers believe that harvest influences North American duck populations based on calls for more conservative harvest regulations. A recent review of harvest and population dynamics of North American mallard (Anas platyrhynchos) populations (Pöysä et al. 2004) reached similar conclusions. Because of the importance of this issue, we reviewed the evidence for an impact of harvest on duck populations. Our understanding of the effects of harvest is limited because harvest effects are typically confounded with those of population density; regulations are typically most liberal when populations are greatest. This problem also exists in the current Adaptive Harvest Management Program (Conn and Kendall 2004). Consequently, even where harvest appears additive to other mortality, this may be an artifact of ignoring effects of population density. Overall, we found no compelling evidence for strong additive effects of harvest on survival in duck populations that could not be explained by other factors.

Journal of Wildlife Management