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USGS2010

Source and fate of inorganic solutes in the Gibbon River, Yellowstone National Park, Wyoming, USA: I. Low-flow discharge and major solute chemistry

The Gibbon River in Yellowstone National Park (YNP) is an important natural resource and habitat for fisheries and wildlife. However, the Gibbon River differs from most other mountain rivers because its chemistry is affected by several geothermal sources including Norris Geyser Basin, Chocolate Pots, Gibbon Geyser Basin, Beryl Spring, and Terrace Spring. Norris Geyser Basin is one of the most dynamic geothermal areas in YNP, and the water discharging from Norris is much more acidic (pH 3) than other geothermal basins in the upper-Madison drainage (Gibbon and Firehole Rivers). Water samples and discharge data were obtained from the Gibbon River and its major tributaries near Norris Geyser Basin under the low-flow conditions of September 2006. Surface inflows from Norris Geyser Basin were sampled to identify point sources and to quantify solute loading to the Gibbon River. The source and fate of the major solutes (Ca, Mg, Na, K, SiO 2 , Cl, F, HCO 3 , SO 4 , NO 3 , and NH 4 ) in the Gibbon River were determined in this study and these results may provide an important link in understanding the health of the ecosystem and the behavior of many trace solutes. Norris Geyser Basin is the primary source of Na, K, Cl, SO 4 , and N loads (35–58%) in the Gibbon River. The largest source of HCO 3 and F is in the lower Gibbon River reach. Most of the Ca and Mg originate in the Gibbon River upstream from Norris Geyser Basin. All the major solutes behave conservatively except for NH 4 , which decreased substantially downstream from Gibbon Geyser Basin, and SiO 2 , small amounts of which precipitated on mixing of thermal drainage with the river. As much as 9–14% of the river discharge at the gage is from thermal flows during this period.

Wyoming↗

USGS2024

Seasonal activity patterns of northern long-eared bats on the coastal Mid-Atlantic

Conservation of bats declining from white-nose syndrome (WNS) impacts requires an understanding of both temporal and landscape-level habitat relationships. Traditionally, much of the research on bat ecology has focused on behavior of summer maternity colonies within species’ distribution cores, including that of the endangered northern long-eared bat ( Myotis septentrionalis ). To further our knowledge of this species, we evaluated multi-season activity patterns in eastern North Carolina and Virginia, including areas where populations were recently discovered. We used passive acoustic monitoring to assess relative and probable activity of northern long-eared bats from October 2016 to August 2021. Northern long-eared bat relative activity was greatest in areas containing greater proportions of woody wetlands and upland pine-dominated evergreen forests. However, the likelihood of recording northern long-eared bats was associated with smaller proportions of woody wetlands and open water resources. Furthermore, we observed a higher probability of recording northern long-eared bats during non-winter seasons. Probable activity was greatest at temperatures between 10 and 25 C, potentially highlighting an optimal thermoneutral zone for the species regionally. Relative activity of northern long-eared bats on the Coastal Plain of Virginia and North Carolina was primarily driven by cover features, whereas probable activity was driven by a combination of cover features, seasonality, and temperature. Therefore, acoustical surveys for this species may be most effective when targeting woody wetlands adjacent to upland forests, particularly upland pine-dominated evergreen stands, during moderate temperatures of non-winter seasons (1 April–15 November). Moreover, conservation of a diverse mosaic of woody wetlands juxtaposed by upland forests may promote both roosting and overwintering habitat, thereby enhancing overwintering survival, maternity colony establishment, and ultimately, successful reproduction of northern long-eared bats.

North Carolina, Virginia↗

USGS2013

Evaluating greater sage-grouse seasonal space use relative to leks: Implications for surface use designations in sagebrush ecosystems

The development of anthropogenic structures, especially those related to energy resources, in sagebrush ecosystems is an important concern among developers, conservationists, and land managers in relation to greater sage-grouse (Centrocercus urophasianus; hereafter, sage-grouse) populations. Sage-grouse are dependent on sagebrush ecosystems to meet their seasonal life-phase requirements, and research indicates that anthropogenic structures can adversely affect sage-grouse populations. Land management agencies have attempted to reduce the negative effects of anthropogenic development by assigning surface use (SU) designations, such as no surface occupancy, to areas around leks (breeding grounds). However, rationale for the size of these areas is often challenged. To help inform this issue, we used a spatial analysis of sage-grouse utilization distributions (UDs) to quantify seasonal (spring, summer and fall, winter) sage-grouse space use in relation to leks. We sampled UDs from 193 sage-grouse (11,878 telemetry locations) across 4 subpopulations within the Bi-State Distinct Population Segment (DPS, bordering California and Nevada) during 2003–2009. We quantified the volume of each UD (vUD) within a range of areas that varied in size and were centered on leks, up to a distance of 30 km from leks. We also quantified the percentage of nests within those areas. We then estimated the diminishing gains of vUD as area increased and produced continuous response curves that allow for flexibility in land management decisions. We found nearly 90% of the total vUD (all seasons combined) was contained within 5 km of leks, and we identified variation in vUD for a given distance related to season and migratory status. Five kilometers also represented the 95th percentile of the distribution of nesting distances. Because diminishing gains of vUD was not substantial until distances exceeded 8 km, managers should consider the theoretical optimal distances for SU designation between 5.0 km and 7.5 km, depending on migratory status. Although these results represent space use for sage-grouse within the Bi-State DPS, our results likely have broad relevance to other areas with similar landscape characteristics and patterns of space use.

Journal of Wildlife Management↗

USGS2016

Population dynamics of mallards breeding in eastern Washington

Variation in regional population trends for mallards breeding in the western United States indicates that additional research into factors that influence demographics could contribute to management and understanding the population demographics of mallards across North America. We estimated breeding incidence and adult female, nest, and brood survival in eastern Washington in 2006 and 2007 by monitoring female mallards with radio telemetry and tested how those parameters were influenced by study year (2006 vs. 2007), landscape type (agricultural vs. natural), and age (second year [SY] vs. after second year [ASY]). We also investigated the effects of female body condition and capture date on breeding incidence, and nest initiation date and hatch date on nest and brood survival, respectively. We included population parameters in a stage-based demographic model and conducted a perturbation analysis to identify which vital rates were most influential on population growth rate (λ). Adult female survival was best modeled with a constant weekly survival rate (0.994, SE = 0.003). Breeding incidence differed between years and was higher for birds in better body condition. Nest survival was higher for ASY females (0.276, SE = 0.118) than SY females (0.066, SE = 0.052), and higher on publicly managed lands (0.383, SE = 0.212) than agricultural (0.114, SE = 0.058) landscapes. Brood survival was best modeled with a constant rate for the 7-week monitoring period (0.50, SE = 0.155). The single variable having the greatest influence on λ was non-breeding season survival, but the combination of parameters from the breeding grounds explained a greater percent of the variance in λ. Mallard population growth rate was most sensitive to changes in non-breeding survival, nest success, brood survival, and breeding incidence. Future management decisions should focus on activities that improve these vital rates if managers want to increase the production of mallards in eastern Washington.

Washington↗

USGS2005

Effects of hunting on survival of American woodcock in the Northeast

Numbers of American woodcock ( Scolopax minor ) males counted on the annual singing ground survey (SGS) have declined over the last 35 years at an average rate of 2.3% per year in the Eastern Region and 1.8% per year in the Central Region. Although hunting was not thought to be a cause of these declines, mortality caused by hunters can be controlled. Furthermore, there has been no research on effects of hunting mortality on woodcock populations at local and regional levels on the breeding grounds. We used radiotelemetry to determine survival rates and causes of mortality for 913 woodcock captured during fall 1997–2000 on 7 areas in Maine, New Hampshire, Pennsylvania, and Vermont, USA. Three of 7 sites were closed to hunting. For all sites and all years combined, 176 woodcock died, and 130 were censored, of which 39 were censored mortalities. Predation was the major ( n = 134, 76%) cause of mortality. Mammals accounted for 56% of the predation, raptors accounted for 25%, and 19% was attributed to unknown predators. On hunted sites, 36% of the total mortality ( n = 102) was caused by hunting, 63% by predation, and 1 bird starved. Kaplan-Meier survival curves did not differ between hunted and non-hunted sites among years ( P = 0.46). Overall, point estimates of survival did not differ ( P = 0.217) between hunted (SR = 0.636, SE = 0.04) and nonhunted sites (SR = 0.661, SE = 0.08). We modeled hazard rates from hunting and natural mortality events using program MARK. Akaike's Information Criterion supported using a model with common constant hazards from both hunting and natural causes for groups of sites. Groupings of sites for hazard rates from natural causes were not influenced by whether a site was hunted or not. Models detected no effects of woodcock age and sex ( P = 0.52) on survival. Proportional hazards models comparing hunted and nonhunted sites found no effects of age and sex ( P = 0.45), interactions of age, sex, capture weight, and bill length ( P ≥ 0.269). Our data suggest that current hunting regulations are not causing lower survival of woodcock.

Maine, New Hampshire, Pennsylvania, Vermont↗

USGS2015

Assessment of environmental DNA for detecting presence of imperiled aquatic amphibian species in isolated wetlands

Environmental DNA (eDNA) is an emerging tool that allows low-impact sampling for aquatic species by isolating DNA from water samples and screening for DNA sequences specific to species of interest. However, researchers have not tested this method in naturally acidic wetlands that provide breeding habitat for a number of imperiled species, including the frosted salamander ( Ambystoma cingulatum ), reticulated flatwoods salamanders ( Ambystoma bishopi ), striped newt ( Notophthalmus perstriatus ), and gopher frog ( Lithobates capito ). Our objectives for this study were to develop and optimize eDNA survey protocols and assays to complement and enhance capture-based survey methods for these amphibian species. We collected three or more water samples, dipnetted or trapped larval and adult amphibians, and conducted visual encounter surveys for egg masses for target species at 40 sites on 12 different longleaf pine ( Pinus palustris ) tracts. We used quantitative PCRs to screen eDNA from each site for target species presence. We detected flatwoods salamanders at three sites with eDNA but did not detect them during physical surveys. Based on the sample location we assumed these eDNA detections to indicate the presence of frosted flatwoods salamanders. We did not detect reticulated flatwoods salamanders. We detected striped newts with physical and eDNA surveys at two wetlands. We detected gopher frogs at 12 sites total, three with eDNA alone, two with physical surveys alone, and seven with physical and eDNA surveys. We detected our target species with eDNA at 9 of 11 sites where they were present as indicated from traditional surveys and at six sites where they were not detected with traditional surveys. It was, however, critical to use at least three water samples per site for eDNA. Our results demonstrate eDNA surveys can be a useful complement to traditional survey methods for detecting imperiled pond-breeding amphibians. Environmental DNA may be particularly useful in situations where detection probability using traditional survey methods is low or access by trained personnel is limited.

Alabama, Florida, Georgia, South Carolina↗

USGS2023

Demographics and gross pathology of scoters and scaups killed by the Cosco Busan oil spill in California

Unusual wildlife mortality events provide a unique opportunity to collect information on demographics, disease, and body condition in affected wildlife, which may be useful for informing oil spill damage assessments and future spill responses. In November 2007, the Cosco Busan Oil Spill occurred in San Francisco Bay, California, a globally important wintering area for waterfowl. The spill resulted in the mortality of scoters Melanitta spp. and scaups Aythya spp., species that have declined significantly over recent decades. We examined the demography (sex and age ratios) and prevalence of grossly apparent disease (acanthocephalan parasite infection and mycotic disease) in 288 Surf Scoters M. perspicillata , White-winged Scoters M. deglandi , Greater Scaup A. marila , and Lesser Scaup A. affinis killed in the oil spill. The proportions of females and juveniles in examined Surf Scoters was unexpectedly high (0.98:1, females:males, 0.73:1 juveniles:adults) for this species with normally strong male- and adult-biased populations. This disproportionate mortality of female Surf Scoters could result in a greater population impact on this female-limited species, suggesting a mechanism for steep declines in San Francisco Bay scoter numbers in the years after the Cosco Busan oil spill. Significantly greater rates of acanthocephalan infection in juvenile vs. adult Surf Scoters indicated a possible interaction between acanthocephalan parasitism and juvenile-biased mortality in our sample. Birds that died during rehabilitation had significantly greater rates of mycotic disease (10% infected) than birds found dead in the field (3%), indicating that infections began or worsened during rehabilitation. Greater Scaup had proportionally greater rates of infection with mycotic disease (26% of individuals) than other species, indicating that they may be particularly susceptible to the disease. We encourage the documentation of demographics and disease as a regular part of future responses to oil spills, or other mortality events, to gain insight into population impacts and improve rehabilitation efforts of affected populations.

California↗

USGS2017

The pathogenesis of clade 2.3.4.4 H5 highly pathogenic avian influenza viruses in Ruddy Duck (Oxyura jamaicensis) and Lesser Scaup (Aythya affinis)

Waterfowl are the natural hosts of avian influenza virus (AIV) and disseminate the virus worldwide through migration. Historically, surveillance and research efforts for AIV in waterfowl have focused on dabbling ducks. The role of diving ducks in AIV ecology has not been well characterized. In this study, we examined the relative susceptibility and pathogenicity of clade 2.3.4.4 H5 highly pathogenic AIV (HPAIV) in two species of diving ducks. Juvenile and adult Ruddy Duck ( Oxyura jamaicensis ) and juvenile Lesser Scaup ( Aythya affinis ) were intranasally inoculated with A/Northern Pintail/WA/40964/2014 H5N2 HPAIV. Additional groups of juvenile Lesser Scaups were inoculated with A/Gyrfalcon/WA/41088/2014 H5N8 HPAIV. The approximate 50% bird infectious doses (BID 50 ) of the H5N2 isolate for adult Ruddy Ducks was <10 2 50% egg infectious doses (EID 50 ) and for the juvenile Lesser Scaups it was <10 4 EID 50 . There were insufficient juvenile Ruddy Ducks to calculate the BID 50 . The BID 50 for the juvenile Lesser Scaups inoculated with the H5N8 isolate was 10 3 EID 50 . Clinical disease was not observed in any group; however, mortality occurred in the juvenile Ruddy Ducks inoculated with the H5N2 virus (three of five ducks), and staining for AIV antigen was observed in numerous tissues from these ducks. One adult Ruddy Duck also died and although it was infected with AIV (the duck was positive for virus shedding and AIV antigen was detected in tissues), it was also infected with coccidiosis. The proportion of ducks shedding virus was related to the dose administered, but the titers were similar among dose groups. The group with the fewest ducks shedding virus was the adult Ruddy Ducks. There was a trend for the Lesser Scaups to shed higher titers of virus than the Ruddy Ducks. No virus shedding was detected after 7 d postinoculation in any group. Similar to dabbling ducks, Lesser Scaups and Ruddy Ducks are susceptible to infection with this H5 HPAIV lineage, although they excrete lower titers of virus.

Journal of Wildlife Diseases↗

USGS2024

Free-roaming horses exceeding appropriate management levels affect multiple vital rates in greater sage-grouse

Since the passage of the Wild Free-Roaming Horses and Burros Act of 1971, federal agencies have been responsible for managing free-roaming equids in the United States. Over the last 20 years, management has been hampered by direct opposition from advocacy groups, budget limitations, and a decline in the public’s willingness to adopt free-roaming horses ( Equus caballus ). As a result, free-roaming equid numbers have increased to more than 3 times the targeted goal of 26,785 (horses and burros [ E. asinus ] combined), the cumulative sum of the Appropriate Management Levels (AML) for all 177 designated Herd Management Areas (HMA) managed by the Bureau of Land Management. Recent research in the Great Basin has implicated these increases as one of the drivers of greater sage-grouse ( Centrocercus urophasianus ) population declines, due to habitat impacts exacerbated by ongoing drought conditions. To evaluate potential demographic mechanisms driving these declines, we compiled survival data from 4 studies in central Wyoming, USA, including 995 adult female (first year breeders or older) sage-grouse during the breeding season, 1,075 nests, 372 broods, and 136 juveniles (i.e., overwinter survival for fledged young), across a 15-year window (2008–2022). During this period, we also obtained population information for free-roaming horses from 9 HMAs used by individual grouse in our sample. Population estimates of free-roaming horses for these HMAs ranged from 59–700% of the maximum appropriate management level (AML max ). Sage-grouse monitored outside of HMAs represented control populations and, because we assumed they were not exposed to populations of free-roaming horses, values of AML max were set to zero for all grouse located outside of HMAs. To evaluate whether free-roaming horses were negatively impacting sage-grouse, we modeled daily survival of breeding age females, nest, broods, and juveniles. We found strong or moderate evidence that overabundant free-roaming horses negatively impacted nest, brood, and juvenile survival. When horse abundance increased to 300% from 100% of AML max , survival was reduced 8.1%, 18.3%, 18.2%, and 18.2% for nests, early broods (≤20 days after hatch), late broods (>20 days to 35 days after hatch), and juveniles, respectively. These results indicate increasing free-roaming horse numbers affected vital rates for critical life stages of sage-grouse, and that maintaining free-roaming horse numbers below AML max would minimize impacts to sage-grouse populations.

Wyoming↗

USGS2017

Developing an effective Agassiz's Desert Tortoise monitoring program: Final report to the Coachella Valley Conservation Commission

Agassiz’s desert tortoise (Gopherus agassizii) is a conservation-reliant species with populations north and west of the Colorado River protected as threatened under the Endangered Species Act (Averill-Murray et al. 2012). Since it was listed under this category in 1990, a great deal has been learned about the natural history of the species, and it is now one of the best-studied turtles in the United States (Lovich and Ennen 2013). However, the accumulated body of scientific data available for the species has not yet been translated into recovery or delisting of the species. Successful conservation of any species requires knowledge of their natural history and how vital rates affect their ability to maintain stable populations in the face of natural and anthropogenic stresses. Agassiz’s desert tortoises occur from southwestern Utah to near the Mexican border in California – a distance of over 450 km – but population densities vary greatly across this immense landscape (U.S. Fish and Wildlife Service 2015). Tortoises occur in the Sonoran Desert of California, including the eastern and western ends of the Coachella Valley, where it is one of 27 species covered under the Coachella Valley Multiple Species Habitat Conservation Plan and Natural Community Conservation Plan (CVMSHCP/NCCP). The southern portion of Joshua Tree National Park (JTNP) lies within this 1.1 million acre planning area, and was predicted to be an area of low-density tortoise populations using habitat suitability modeling (Barrows 2011). JTNP is near the southern distributional limit of G. agassizii, yet very little has been published regarding the ecology of tortoises in the Sonoran Desert of California. Reproductive output is an important gross measure of the ability of a population to persist. When integrated with data on fertility and survivorship, this information forms a foundation for assessing population status and formulating effective management strategies (e.g., Congdon et al. 1993, 1994), especially for imperiled species. One aspect of the biology of G. agassizii that has been particularly well-studied is reproductive output. However, most of what we know about this topic comes from research in the Mojave Desert portion of the species’ range (Ernst and Lovich 2009). Comparatively little has been published on the reproductive ecology of populations living in the Sonoran Desert ecosystem of California. Publications by Lovich et al. (1999, 2011, 2012, 2014, 2015) constitute the main body of literature on desert tortoise reproductive ecology in the Sonoran Desert of California, with one study population located at the western end of the CVMSHCP/NCCP area. Collecting data on Agassiz’s desert tortoise ecology in the Sonoran Desert ecosystem is important due to significant differences between the two adjacent desert ecosystems, especially the timing and amounts of annual precipitation, and their potential effects on reproductive output (e.g., Lovich et al. 5 2015). There are also differences in the vulnerability of tortoises to the effects of a warming, drying climate between the two deserts (Barrows 2011; Zylstra et al. 2012). The overall goal of this study was to collect data on demography, reproductive output, and genetic affinities at a study site in the Sonoran Desert portion of JTNP in the eastern end of the CVMSHCP/NCCP area. Specific objectives included: 1) Collect data to establish baselines on tortoise populations and/or their habitat suitability in core habitat within the CVNCCP area, including biotic and abiotic variables affecting persistence of tortoise populations; 2) Compare and contrast with data collected on desert tortoises at USGS/BLM study site near Palm Springs over 16 years; 3) Support long-term modeling efforts needed to determine tortoise population viability; 4) Refine modeled relationships with identified threats such as fire, invasive species and climate change; and 5) Prioritize adaptive management needs for the desert tortoise in and beyond the CVNCCP area. The data from this study will aid in determining baseline estimates of the desert tortoise population size within the planning area as well as establish a marked population of Agassiz’s desert tortoises for future monitoring. Data will be integrated with habitat modeling in order to refine model output. Genetic data will be collected on both the north and south sides of Interstate 10 to determine the potential effects of habitat fragmentation and genetic mixing. Analyses are ongoing and results beyond those presented in this report will be published in peer-reviewed scientific journals following inclusion of additional data collected on the south side of Shavers Valley in 2017-2018.

Report↗

USGS2017

Effects of tow transit on the efficacy of the Chicago Sanitary and Ship Canal Electric Dispersal Barrier System

In 2016, the U.S. Fish and Wildlife Service, U.S. Geological Survey, and U.S. Army Corps of Engineers undertook a field study in the Chicago Sanitary and Ship Canal near Romeoville, Illinois to determine the influence of tow transit on the efficacy of the Electric Dispersal Barrier System (EDBS) in preventing the passage of juvenile fish (total length < 100 millimeters (mm)). Dual-frequency identification sonar data showed that large schools of juvenile fish (mean school size of 120 fish; n = 19) moved upstream and crossed the electric field of an array in the EDBS concurrent with downstream-bound (downbound) loaded tows in 89.5% of trials. Smaller schools of juvenile fish (mean school size of 98 fish; n = 15) moved downstream and crossed the electric field of an array in the EDBS concurrent with upstream-bound (upbound) loaded tows in 73.3% of trials. Observed fish passages through the EDBS were always opposite to the direction of tow movement, and not associated with propeller wash. These schools were not observed to breach the EDBS in the absence of a tow and showed no signs of incapacitation in the barrier during tow passage. Loaded tows transiting the EDBS create a return current of water flowing between the tow and the canal wall that typically travels opposite the direction of tow movement, and cause a decrease in the voltage gradient of the barrier of up to 88%. Return currents and decreases in voltage gradients induced by tow passage likely contributed to the observed fish passage through the EDBS. The efficacy of the EDBS in preventing the passage of small, wild fish is compromised while tows are moving across the barrier system. In particular, downbound tows moving through the EDBS create a pathway for the upstream movement of small fish, and therefore may increase the risk of transfer of invasive fishes from the Mississippi River Basin to the Great Lakes Basin.

Illinois↗

USGS2023

Modeling the spatial distribution of carcasses of eagles killed by wind turbines

Currently, the US Fish and Wildlife Service makes eagle permitting and management decisions nationwide based on a limited understanding of the impacts of wind power generation on eagles, and the factors that influence risk at a given facility. Accurate estimates of eagle mortality at wind power facilities form the basis for comparing the magnitudes of mortality rates in different areas and for measuring the benefits of proposed methods of minimizing the collision-caused impacts to eagle populations. Simple counts of observed eagle carcasses at wind facilities are almost certainly underestimates of the true mortality because fatalities can be removed by scavengers, be missed by searchers, or fall outside searched areas. For the latter, models of relative carcass density as a function of distance from the turbine can be fit to observed carcass locations and used to estimate the proportion of carcasses expected to land within an area of any configuration beneath a turbine. In the USA, however, it has been difficult to estimate these models for large birds such as Bald Eagles ( Haliaeetus leucocephalus ) and Golden Eagles ( Aquila chrysaetos ) due to inadequate numbers of dead eagles found at any single facility. In this case, analysis of a surrogate species might be useful to inform carcass distributions. We chose to model the carcass distribution of White-tailed Eagles ( Haliaeetus albicilla ) in Norway as an informative surrogate for Bald Eagles and Golden Eagles in the USA. Our three best-fitting parametric models were very consistent in estimating that 50% (95% CI: 40–60%) of White-tailed Eagle carcasses land within approximately 42 m of the turbines that had 70-m hubs and approximately 40-m blades. Although our models were fit to data from White-tailed Eagles and not Bald or Golden Eagles, applying these models when calculating mortality impacts of wind developments on both eagle species will likely improve the accuracy of post-construction mortality estimates, particularly at sites where substantial areas may be unsearchable. Accurate post-construction mortality estimates can inform pre-construction fatality prediction models. Resource managers can determine whether their conditions are sufficiently similar to those we modeled to warrant the use of these models for Bald and Golden Eagle carcass distributions.

Journal of Raptor Research↗

USGS2021

Annual-cycle movements and phenology of black scoters in eastern North America

Sea ducks exhibit complex movement patterns throughout their annual cycle; most species use distinct molting and staging sites during migration and disjunct breeding and wintering sites. Although research on black scoters ( Melanitta americana ) has investigated movements and habitat selection during winter, little is known about their annual-cycle movements. We used satellite telemetry to identify individual variation in migratory routes and breeding areas for black scoters wintering along the Atlantic Coast, to assess migratory connectivity among wintering, staging, breeding, and molt sites, and to examine effects of breeding site attendance on movement patterns and phenology. Black scoters occupied wintering areas from Canadian Maritime provinces to the southeastern United States. Males used an average of 2.5 distinct winter areas compared to 1.1 areas for females, and within-winter movements averaged 1,256 km/individual. Individuals used an average of 2.1 staging sites during the 45-day pre-breeding migration period, and almost all were detected in the Gulf of St. Lawrence. Males spent less time at breeding sites and departed them earlier than females. During post-breeding migration, females took approximately 25 fewer days than males to migrate from breeding sites to molt and staging sites, and then wintering areas. Most individuals used molt sites in James and Hudson bays before migrating directly to coastal wintering sites, which took approximately 11 days and covered 1,524 km. Males tended to arrive at wintering areas 10 days earlier than females. Individuals wintering near one another did not breed closer together than expected by chance, suggesting weak spatial structuring of the Atlantic population. Females exhibited greater fidelity (4.5 km) to previously used breeding sites compared to males (60 km). A substantial number of birds bred west of Hudson Bay in the Barrenlands, suggesting this area is used more widely than believed previously. Hudson and James bays provided key habitat for black scoters that winter along the Atlantic Coast, with most individuals residing for >30% of their annual cycle in these bays. Relative to other species of sea duck along the Atlantic Coast, the Atlantic population of black scoter is more dispersed and mobile during winter but is more concentrated during migration. These results could have implications for future survey efforts designed to assess population trends of black scoters.

Chesapeake Bay, Delaware Bay, Gulf of St Lawrence,↗

USGS2010

Depletion of rice as food of waterfowl wintering in the Mississippi Alluvial Valley

Waterfowl habitat conservation strategies in the Mississippi Alluvial Valley (MAV) and several other wintering areas assume carrying capacity is limited by available food, and increasing food resources is an effective conservation goal. Because existing research on winter food abundance and depletion is insufficient to test this hypothesis, we used harvested rice fields as model foraging habitats to determine if waste rice seed is depleted before spring migration. We sampled rice fields ( n = 39 [winter 2000–2001], n = 69 [2001–2002]) to estimate seed mass when waterfowl arrived in late autumn and departed in late winter. We also placed exclosures in subsets of fields in autumn ( n = 8 [2000–2001], n = 20 [2001–2002]) and compared seed mass inside and outside exclosures in late winter to estimate rice depletion attributable to waterfowl and other processes. Finally, we used an experiment to determine if the extent of rice depletion differed among fields of varying initial abundance and if the seed mass at which waterfowl ceased foraging or abandoned fields differed from a hypothesized giving-up value of 50 kg/ha. Mean seed mass was greater in late autumn 2000 than 2001 (127.0 vs. 83.9 kg/ha; P = 0.018) but decreased more during winter 2000–2001 than 2001–2002 (91.3 vs. 55.7 kg/ha) and did not differ at the end of winter (35.8 vs. 28.3 kg/ha; P = 0.651). Assuming equal loss to deterioration inside and outside exclosures, we estimated waterfowl consumed 61.3 kg/ha (48.3%) of rice present in late autumn 2000 and 21.1 kg/ha (25.1%) in 2001. When we manipulated late-autumn rice abundance, mean giving-up mass of rice seed was similar among treatments (48.7 kg/ha; P = 0.205) and did not differ from 50 kg/ha ( P = 0.726). We integrated results by constructing scenarios in which waterfowl consumed rice at different times in winter, consumption and deterioration were competing risks, and consumption occurred only above 50 kg/ha. Results indicated waterfowl likely consumed available rice soon after fields were flooded and the amount consumed exceeded our empirical estimates but was ≤48% (winters pooled) of rice initially present. We suggest 1) using 50 kg/ha as a threshold below which profitability limits waterfowl feeding in MAV rice fields; 2) reducing the current estimate (130 kg/ha) of rice consumed in harvested fields to 47.2 kg/ha; and 3) increasing available rice by increasing total area of fields managed, altering management practices (e.g., staggered flooding), and exploring the potential for producing second or ratoon rice crops for waterfowl.

Arkansas;Illinois;Kentucky;Louisiana;Mississippi;M↗

USGS2025

Estimated annual abundance of migratory Peale's Peregrine Falcons in coastal Washington, USA

Following the recovery of Peregrine Falcons ( Falco peregrinus ), the US Fish and Wildlife Service began a process to allow “take” (capture) of wild peregrines for falconry in the United States. Recently, that effort involved generating updated estimates of the collective abundance of the three North American peregrine subspecies: F. p. anatum , F. p. tundrius , and F. p. pealei (Peale's Peregrine Falcon). Because of the more limited distribution of F. p. pealei , we conducted an analysis specific to its geographic range. We analyzed data from a long-term banding and resighting program on three beaches on the southern coast of Washington, USA, to estimate the annual abundance of migrating and overwintering F. p. pealei , using the capture histories of 250 Peregrine Falcons, nearly all of which were captured during 1277 vehicle surveys between 1995 and 2024. Because we studied an open population of migratory individuals, we used a zero-inflated Poisson log-normal mark-resight model to estimate annual abundance. For the analyses, we partitioned our survey data into sighting periods, each of which extended from 1 September of one year to 31 May of the next. We anticipated that first-year F. p. pealei would be identified for falconry take, and our annual abundance estimates for first-year birds of this subspecies ranged from a high of 24.8 ± 6.1 (SE) individuals in the 2014–2015 sighting period to a low of 1.9 ± 1.4 individuals in the 2023–2024 sighting period. Peregrine Falcon abundance varied annually and appeared to decline during the last two sighting periods. Our sighting rate of marked peregrines was negatively associated with Bald Eagle ( Haliaeetus leucocephalus ) encounter rate. There was a lesser relationship to human activity, and we suspect the change in sighting rate was a behavioral response by Peregrine Falcons to the threat of kleptoparasitism by Bald Eagles. We currently lack comprehensive information about the natal origin of the individual peregrines in our study area, which prevented us from assessing the degree to which falconry take from the pool of falcons migrating to or through Washington might potentially impact local or regional abundances. Although a better understanding of natal origins is needed, our data add clarity to the migration and overwinter abundance of F. p. pealei on the Washington coast and may inform decisions about the take of this subspecies for falconry.

Washington↗