SEARCH · USGS Science

Results for “Bird Populations”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,621 records · Page 90Linked to original sources

USGS2000

Approaches for assessment of terrestrial vertebrate responses to contaminants: moving beyond individual organisms

Conclusions: A need for a broader range ofinformation on effects of contaminants on individuals exists among the 4 classes of terrestrial vertebrates, especially mammals, reptiles, and amphibians. Separation of contaminant effects from other effects and reduction of speculative extrapolation within and among species requires information that can be produced only by combined field and laboratory investigations that incorporate seasonal or annual cycles and important spatial and interaction conditions. Assessments of contaminant effects at the population level and higher are frequently dependent on extrapolations from a lower organizational level. Actual measurements of the effects of contaminants on populations or communities, possibly in conjunction with case studies that establish relations between effects on individuals and effects on populations, are needed to reduce the uncertainty associated with these extrapolations. Associated with these assessment levels is the need for acceptable definitions of what we mean when we refer to a 'meaningful population change' or an 'effect on communities or ecosystems.' At these higher levels of organization we are also confronted with the need for procedures useful for separating contaminant effects from effects caused by other environmental conditions. Although the bulk of literature surveyed was of the focused cause-and-effect type that is necessary for proving relations between contaminants and wildlife, community or ecosystem field assessments, as sometimes performed with reptiles and amphibians, might be a useful alternative for estimating the potential of a contaminant to cause environmental harm. Assumptions about the special usefulness of reptiles and amphibians as environmental indicators ought to be tested with comparisons to mammals and birds. Information on the effects of contaminants above the individual level is needed to generate accurate estimates of the potential consequences of anthropogenic pollution (e.g., ecological risk assessments). However, realized population, or higher, levels of effects should not be part of regulatory guidelines because the threshold of harm would be too high to be used as a catalyst for action. Measures of realized population or community effects could be used to evaluate the effectiveness of regulatory actions and assess chronic or difficult environmental problems. Some of these information needs can be satisfied with modest effort and expense, but much of the suggested work that incorporates great complexity or long duration is likely to be difficult to accomplish. Cooperation among investigators with different specialties and a willingness by government, academia, and corporate organizations to support the most challenging work will be necessary. Because we are unlikely to have the financial resources to evaluate more than a small number of contaminants for effects at the levels of population, community, or ecosystem, we might need to thoroughly study a few contaminants and then extend the findings to functionally similar contaminants. If sufficient cooperation and organizational support does not materialize, the pursuit of estimation methods will overshadow the collection of actual information on relations between contaminants and wildlife.

Book chapter↗

USGS2017

Shifts in an invasive rodent community favoring black rats (Rattus rattus) following restoration of native forest

One potential, unintended ecological consequence accompanying forest restoration is a shift in invasive animal populations, potentially impacting conservation targets. Eighteen years after initial restoration (ungulate exclusion, invasive plant control, and out planting native species) at a 4 ha site on Maui, Hawai'i, we compared invasive rodent communities in a restored native dry forest and adjacent non-native grassland. Quarterly for 1 year, we trapped rodents on three replicate transects (107 rodent traps) in each habitat type for three consecutive nights. While repeated trapping may have reduced the rat (Black rat, Rattus rattus ) population in the forest, it did not appear to reduce the mouse (House mouse, Mus musculus ) population in the grassland. In unrestored grassland, mouse captures outnumbered rat captures 220:1, with mice averaging 54.9 indiv./night versus rats averaging 0.25 indiv./night. In contrast, in restored native forest, rat captures outnumbered mouse captures by nearly 5:1, averaging 9.0 indiv./night versus 1.9 indiv./night for mice. Therefore, relatively recent native forest restoration increased Black rat abundance and also increased their total biomass in the restored ecosystem 36-fold while reducing House mouse biomass 35-fold. Such a community shift is worrisome because Black rats pose a much greater threat than do mice to native birds and plants, perhaps especially to large-seeded tree species. Land managers should be aware that forest restoration (i.e. converting grassland to native forest) can invoke shifts in invasive rodent populations, potentially favoring Black rats. Without intervention, this shift may pose risks for intended conservation targets and modify future forest restoration trajectories.

Restoration Ecology↗

USGS2009

Estimating survival of precocial chicks during the prefledging period using a catch-curve analysis and count-based age-class data

Estimating reproductive success for birds with precocial young can be difficult because chicks leave nests soon after hatching and individuals or broods can be difficult to track. Researchers often turn to estimating survival during the prefledging period and, though effective, mark-recapture based approaches are not always feasible due to cost, time, and animal welfare concerns. Using a threatened population of Piping Plovers (Charadrius melodus) that breeds along the Missouri River, we present an approach for estimating chick survival during the prefledging period using long-term (1993-2005), count-based, age-class data. We used a modified catch-curve analysis, and data collected during three 5-day sampling periods near the middle of the breeding season. The approach has several ecological and statistical assumptions and our analyses were designed to minimize the probability of violating those assumptions. For example, limiting the sampling periods to only 5 days gave reasonable assurance that population size was stable during the sampling period. Annual daily survival estimates ranged from 0.825 (SD = 0.03) to 0.931 (0.02) depending on year and sampling period, with these estimates assuming constant survival during the prefledging period and no change in the age structure of the population. The average probability of survival to fledging ranged from 0.126 to 0.188. Our results are similar to other published estimates for this species in similar habitats. This method of estimating chick survival may be useful for a variety of precocial bird species when mark-recapture methods are not feasible and only count-based age class data are available. ?? 2009 Association of Field Ornithologists.

Journal of Field Ornithology↗

USGS2007

Philopatry: A return to origins

The word “philopatry” is a combination of the prefix philo (from the Greek philos, “beloved”) and the Latin patria, which means “fatherland” or “homeland.” Since the first English-language use of “philopatry” in an ornithological context by Huntington (1951) , the term has been applied to two types of site-faithful behavior in birds. Closest to the etymological meaning is the first, “natal philopatry,” which means not dispersing far from, or returning to, a birthplace for reproduction. The second is “breeding philopatry,” which means returning to the same breeding area each year, though that area may not be an individual’s birth place ( Shields 1982 , Anderson et al. 1992 ). Therefore, any assessment of breeding philopatry likely includes some immigrant individuals, whereas assessments of natal philopatry include only locally hatched or born individuals. In the past several years, the use of philopatry in the ornithological literature has widened further, to include site fidelity to nonbreeding areas, such as sites used for molting ( Iverson et al. 2004 ), wintering ( Robertson and Cooke 1999 , Mehl et al. 2004 ), or stopover during migration ( Merom et al. 2000 ). Use of the term “philopatry” to describe not only natal homing, but general site fidelity to both breeding and nonbreeding sites of individuals whose natal areas are unknown is, I believe, problematic and warrants reconsideration. This is because there are substantial genetic and demographic implications of philopatry in its purest and historical sense (i.e., natal philopatry), such as increased relatedness and population differentiation ( Greenwood 1980 , Quinn and White 1987 , Avise et al. 1992 ). Indeed, the historical and theoretical discussions of natal philopatry focus on the behavior of limited dispersal from a birth place, how this promotes inbreeding, why inbreeding might be adaptive, and how a lack of gene flow might promote speciation ( Mayr 1963 , Shields 1982 , Anderson et al. 1992 ). I believe that these population-genetic and demographic implications are potentially misapplied when “philopatry” is used to describe site-faithful behavior in general (see Pearce and Talbot 2006 ). The potential danger of applying philopatry to non-natal and nonbreeding conditions is that it creates the expectation of certain outcomes, such as low dispersal rates, population genetic differentiation, and unique population segments, when such conditions may not exist. Given that most avian species do not molt, winter, or have migratory stopovers where they breed, I propose that the term “philopatry” and its genetic expectations be used only in relation to natal philopatry and not extended to (1) breeding- site fidelity of individuals whose natal areas are unknown and (2) nonbreeding areas where site- faithful behavior is observed. I believe this correctly distinguishes natal philopatry as a specific type of site fidelity with its own implications for population genetics and dynamics. Thus, philopatry should be viewed as synonymous and interchangeable with the terms “natal-site fidelity” and “natal philopatry,” and the term “breeding-site fidelity” should replace “breeding philopatry,” because it reflects the unknown natal origins of birds captured as adults. Although the broader condition of site fidelity may have implications for fitness, mate pairing, and population delineation—as examined in several studies ( Robertson and Cooke 1999 , Merom et al. 2000 , Iverson et al. 2004 , Mehl et al. 2004 )—future investigations of site fidelity should be pursued without automatically invoking the term “philopatry” and assuming that the genetic and demographic connotations of natal philopatry also apply. In contrast to philopatry, the probability of fidelity ( F ) and dispersal (1 − F ) are estimable parameters ( Burnham 1993 , Kendall and Nichols 2004 ), and the demographic and genetic consequences of site fidelity, regardless of where it occurs, can serve as hypotheses for testing with multiple data types (e.g., Arsenault et al. 2005 ). Such data mergers should enhance our understanding of the demographic, behavioral, and genetic implications of natal philopatry and site fidelity.

The Auk↗

USGS2026

A practical decision tool for marine bird mortality assessments

Given the rise in anthropogenic, environmental, and disease events contributing to marine bird mortality, there is a critical need to improve the rigor of mortality assessments. Deficits in data collection and mortality estimation can hinder a manager’s ability to document the scale of events and assess population level impacts. Therefore, to inform decisions required during activities, such as conservation status assessments or harvest management, organizations may choose to incorporate mortality assessments into response plans. Resources, capacity, and assets to assess mortality vary across jurisdictions (federal, state, Indigenous, local, etc.), and clear guidance to support mortality assessments is often unavailable or not clearly addressed. Here, we present a decision support tool to help managers identify and evaluate survey options to assess bird mortality in a diverse array of scenarios. The objective of the decision tool is to improve data collection and availability, which will increase the ability to estimate mortality robustly, given situation-specific attributes and constraints. This decision tool is designed to guide the response when a mortality event is initially encountered and offers suggestions for assessment and reporting procedures in the absence of other guidance or to complement existing protocols. The decision tool is also meant to inform decision making for response determination and resource allocation. The tool facilitates examination of options for further assessment and monitoring, which users determine by examining questions pertaining to species prioritization, determination of mortality minimum spatial extent, and the potential magnitude of impacts on affected species. Finally, identification of appropriate survey methods that address imperfect detection when a complete census is not possible are determined by exploring location, spatial and temporal extent, and the type of species affected. Ultimately, this decision tool aims to facilitate and improve the standardization of mortality assessments, equipping managers with a practical resource to navigate the decision-making process for marine bird mortality estimation.

Ornithological Applications↗

USGS2020

High frequency of lead exposure in the population of an endangered Australian top predator, the Tasmanian wedge-tailed eagle (Aquila audax fleayi)

Lead poisoning, mainly through incidental ingestion of lead ammunition in carcasses, is a threat to scavenging and predatory bird species worldwide. In Australia, shooting for animal control is widespread, and a range of native scavenging species are susceptible to lead exposure. However, the prevalence of lead exposure in Australia's scavenging and predatory birds is largely unknown. We evaluated the degree to which the Tasmanian wedge‐tailed eagle ( Aquila audax fleayi ), an endangered Australian raptor and facultative scavenger, showed evidence of lead exposure. We detected lead in 100% of femur and liver tissues of 109 eagle carcasses opportunistically collected throughout Tasmania between 1996 and 2018. Concentrations were elevated in 10% of 106 liver (> 6 mg/kg dw) and 4% of 108 femur (> 10 mg/kg dw) samples. We also detected lead in 96% of blood samples taken from 24 live nestlings, with 8% at elevated concentrations (> 10 μg/dL). Of the liver samples with elevated lead, 73% had lead 207/206 isotope ratios within the published range of lead‐based bullets available in Tasmania. These first comprehensive data on lead exposure of an Australian raptor are comparable to those for raptor studies elsewhere that identify lead‐based ammunition exposure as a conservation threat. Our findings highlight the importance of further research and efforts to address lead contamination throughout the Tasmanian ecosystem and in other Australian regions.

Environmental Toxicology and Chemistry↗

USGS2010

Population structure and plumage polymorphism: the intraspecific evolutionary relationships of a polymorphic raptor, Buteo jamaicensis harlani

Background Phenotypic and molecular genetic data often provide conflicting patterns of intraspecific relationships confounding phylogenetic inference, particularly among birds where a variety of environmental factors may influence plumage characters. Among diurnal raptors, the taxonomic relationship of Buteo jamaicensis harlani to other B. jamaicensis subspecies has been long debated because of the polytypic nature of the plumage characteristics used in subspecies or species designations. Results To address the evolutionary relationships within this group, we used data from 17 nuclear microsatellite loci, 430 base pairs of the mitochondrial control region, and 829 base pairs of the melanocortin 1 receptor ( Mc1r ) to investigate molecular genetic differentiation among three B. jamaicensis subspecies ( B. j. borealis , B. j. calurus , B. j. harlani ). Bayesian clustering analyses of nuclear microsatellite loci showed no significant differences between B. j. harlani and B. j. borealis . Differences observed between B. j. harlani and B. j. borealis in mitochondrial and microsatellite data were equivalent to those found between morphologically similar subspecies, B. j. borealis and B. j. calurus , and estimates of migration rates among all three subspecies were high. No consistent differences were observed in Mc1r data between B. j. harlani and other B. jamaicensis subspecies or between light and dark color morphs within B. j. calurus , suggesting that Mc1r does not play a significant role in B. jamaicensis melanism. Conclusions These data suggest recent interbreeding and gene flow between B. j. harlani and the other B. jamaicensis subspecies examined, providing no support for the historical designation of B. j. harlani as a distinct species.

BMC Evolutionary Biology↗

USGS2000

Disruption and restoration of en route habitat, a case study: The Chenier Plain

Cheniers (relict beach ridges) and other habitats adjacent to ecological barriers may be critical linkages in the migratory pathways of long-distance migratory birds. It is important that these wooded habitats provide enough food and cover at the right time to support these birds’ requirements. To date, little attention has been given to the conservation of coastal woodlands, habitats in which en route migrants tend to concentrate in large numbers during migration. Because about one-third of North Americas ’ human population lives within 80 km of the coast, many forest-dwelling landbird migrants now depend on degraded native woodlands and urbanized environments for survival during migration. Restoration or rehabilitation of coastal woodlands, such as the cheniers of southwest Louisiana and southeast Texas, is of particular importance because of historic anthropogenic modifications, their limited geographic extent, and the extraordinary abundance and species richness of migratory birds using them during migration. In this paper, we use the Chenier Plain as a case study to discuss the issue of land use changes and their consequences for maintaining suitable stopover habitat. Results from an ongoing field study in this ecosystem indicate that most forest-dependent migratory birds are tolerant of at least some degradation of chenier forest during migration. However, these results reveal that subtle differences in vegetation composition and structure beneath the canopy of these forests, primarily as a result of livestock grazing and white-tailed deer overbrowsing, can result in differential use by some en route migrants. Species that were most affected by disturbance to the forest understory were early-arriving migrants, dead-leaf foragers, frugivores, and nectarivores. Given that the understory structure and regeneration of chenier forests has been so greatly reduced, and that high densities of nearctic-neotropical migrants tend to concentrate in cheniers during migration, restoration and re-habilitation should be conservation priorities in the Chenier Plain.

Louisiana, Texas↗

USGS2013

Evidence of territoriality and species interactions from spatial point-pattern analyses of subarctic-nesting geese

Quantifying spatial patterns of bird nests and nest fate provides insights into processes influencing a species’ distribution. At Cape Churchill, Manitoba, Canada, recent declines in breeding Eastern Prairie Population Canada geese ( Branta canadensis interior ) has coincided with increasing populations of nesting lesser snow geese ( Chen caerulescens caerulescens ) and Ross’s geese ( Chen rossii ). We conducted a spatial analysis of point patterns using Canada goose nest locations and nest fate, and lesser snow goose nest locations at two study areas in northern Manitoba with different densities and temporal durations of sympatric nesting Canada and lesser snow geese. Specifically, we assessed (1) whether Canada geese exhibited territoriality and at what scale and nest density; and (2) whether spatial patterns of Canada goose nest fate were associated with the density of nesting lesser snow geese as predicted by the protective-association hypothesis. Between 2001 and 2007, our data suggest that Canada geese were territorial at the scale of nearest neighbors, but were aggregated when considering overall density of conspecifics at slightly broader spatial scales. The spatial distribution of nest fates indicated that lesser snow goose nest proximity and density likely influence Canada goose nest fate. Our analyses of spatial point patterns suggested that continued changes in the distribution and abundance of breeding lesser snow geese on the Hudson Bay Lowlands may have impacts on the reproductive performance of Canada geese, and subsequently the spatial distribution of Canada goose nests.

PLoS ONE↗

USGS1997

Effects of drought and prolonged winter on Townsend's ground squirrel demography in shrubsteppe habitats

During a mark–recapture study of Townsend's ground squirrels ( Spermophilus townsendii ) on 20 sites in the Snake River Birds of Prey National Conservation Area, Idaho, in 1991 through 1994, 4407 animals were marked in 17639 capture events. This study of differences in population dynamics of Townsend's ground squirrels among habitats spanned a drought near the extreme of the 130-yr record, followed by prolonged winter conditions. Townsend's ground squirrels have a short active season (≈4 mo) in which to reproduce and store fat for overwintering. Their food consists largely of succulent grasses and forbs in this dry shrubsteppe and grassland habitat. The drought in the latter half of the 1992 active season produced early drying of Sandberg's bluegrass ( Poa secunda ) and was associated with low adult and juvenile body masses prior to immergence into estivation/hibernation. The following prolonged winter was associated with late emergence of females in 1993. Early-season body masses of adults were low in 1993 relative to 1992, whereas percentage of body fat in males was relatively high. These weather patterns in spring 1992 and winter 1993 also resulted in reduced adult persistence through the ≈7-mo inactive period, especially for adult females, and near-zero persistence of >1200 juveniles. Consequently, densities of Townsend's ground squirrels across the 20 livetrap sites declined. The demographic effects of drought and prolonged winter lasted at least through the subsequent breeding season. Adult females that survived these weather extremes produced fewer emergent young per female than did adult females prior to the event. Prior to the drought/prolonged winter, yearling female body masses were higher than, or indistinguishable from, those of adults. Females produced in 1993 had lower body masses as yearlings than did adult females. Demographic response to the drought and prolonged winter varied with habitat; ground squirrels in sagebrush habitat showed less decline in persistence and density and produced more young per female during the next active season following the drought (1993) than did ground squirrels in grassland habitat, where densities had been significantly higher prior to the drought and prolonged winter. Studies involving habitat comparisons of animal demography should always be placed in the context of long-term weather patterns, because habitat quality rankings based on density, reproduction, and survival may differ with environmental conditions. Physiological effects of environmental “crunches” on consumers may persist beyond the period of influence on food resources, reducing reproductive success and growth rates of future offspring.

Idaho↗

USGS2012

Allowable levels of take for the trade in Nearctic songbirds

The take of Nearctic songbirds for the caged-bird trade is an important cultural and economic activity in Mexico, but its sustainability has been questioned. We relied on the theta-logistic population model to explore options for setting allowable levels of take for 11 species of passerines that were subject to legal take in Mexico in 2010. Because estimates of population size necessary for making periodic adjustments to levels of take are not routinely available, we examined the conditions under which a constant level of take might contribute to population depletion (i.e., a population below its level of maximum net productivity). The chance of depleting a population is highest when levels of take are based on population sizes that happen to be much lower or higher than the level of maximum net productivity, when environmental variation is relatively high and serially correlated, and when the interval between estimation of population size is relatively long (≥5 years). To estimate demographic rates of songbirds involved in the Mexican trade we relied on published information and allometric relationships to develop probability distributions for key rates, and then sampled from those distributions to characterize the uncertainty in potential levels of take. Estimates of the intrinsic rate of growth (r) were highly variable, but median estimates were consistent with those expected for relatively short-lived, highly fecund species. Allowing for the possibility of nonlinear density dependence generally resulted in allowable levels of take that were lower than would have been the case under an assumption of linearity. Levels of take authorized by the Mexican government in 2010 for the 11 species we examined were small in comparison to relatively conservative allowable levels of take (i.e., those intended to achieve 50% of maximum sustainable yield). However, the actual levels of take in Mexico are unknown and almost certainly exceed the authorized take. Also, the take of Nearctic songbirds in other Latin American and Caribbean countries ultimately must be considered in assessing population-level impacts.

Ecological Applications↗

USGS2014

Characteristics of sandhill crane roosts in the Sacramento-San Joaquin delta of California

The Sacramento-San Joaquin Delta (Delta) region of California is an important wintering region for 2 subspecies of Pacific Flyway sandhill cranes ( Grus canadensis ): the Central Valley Population of the greater sandhill crane ( G. c. tabida ) and the Pacific Flyway Population of the lesser sandhill crane ( G. c. canadensis ). During the winters of 2007-08 and 2008-09 we conducted roost counts, roadside surveys, aerial surveys, and tracked radio-marked birds to locate and assess important habitats for roosting cranes in the Delta. Of the 69 crane night roosts we identified, 35 were flooded cropland sites and 34 were wetland sites. We found that both larger individual roost sites and larger complexes of roost sites supported larger peak numbers of cranes. Water depth used by roosting cranes averaged 10 cm (range 3-21 cm, mode 7 cm) and was similar between subspecies. We found that cranes avoided sites that were regularly hunted or had high densities of hunting blinds. We suggest that managers could decide on the size of roost sites to provide for a given crane population objective using a ratio of 1.5 cranes/ha. The fact that cranes readily use undisturbed flooded cropland sites makes this a viable option for creation of roost habitat. Because hunting disturbance can limit crane use of roost sites we suggest these 2 uses should not be considered readily compatible. However, if the management objective of an area includes waterfowl hunting, limiting hunting to low blind densities and restricting hunting to early morning may be viable options for creating a crane-compatible waterfowl hunt program.

California↗

USGS2020

Prioritizing habitats based on abundance and distribution of molting waterfowl in the Teshekpuk Lake Special Area of the National Petroleum Reserve, Alaska

The National Petroleum Reserve in Alaska (NPR-A) encompasses more than 9.5 million hectares of federally managed land on the Arctic Coastal Plain of northern Alaska, where it supports a diversity of wildlife, including millions of migratory birds. Within the NPR-A, Teshekpuk Lake and the surrounding area provide important habitat for migratory birds, including large numbers of waterfowl and shorebirds that use the area for breeding and molting. This area has been designated by the Bureau of Land Management as the Teshekpuk Lake Special Area (TLSA) and is estimated to host 22 percent of the entire Pacific black brant ( Branta bernicla nigricans ) population as it undergoes flightless wing molt. Additionally, numerous other waterfowl species use the area for breeding and molting, including greater white-fronted geese ( Anser albifrons ), snow geese ( Chen caerulescens ), Canada geese ( Branta hutchinsii ), and tundra swans ( Cygnus columbianus ). A data-derived procedure was developed to define important habitats based on recent distributions of molting birds. That procedure was used to identify areas that could be prioritized for exclusion from oil and gas development within a pre-defined “Goose Molting Area” in the TLSA. This analysis was requested by the Bureau of Land Management to provide information for the development of alternative scenarios for an updated NPR-A, Integrated Activity Plan/Environmental Impact Statement. Habitat selections were based on the population densities of Pacific black brant and Canada geese and pre-defined thresholds for the minimum fraction of the population contained within selected areas. Selections were based on long-term records of population density combined with global-positioning system data to reveal small-scale patterns of habitat use. The highest population density of the Pacific black brant was found along the Beaufort Sea coast on the eastern edge of the study area, whereas Canada geese were somewhat more widely distributed. Depending on the selection criteria and width of protective buffers placed around selected habitat units, 52–85 percent of the Goose Molting Area was identified as high-priority habitat. The effectiveness of this approach to habitat protection assumes that buffers around selected habitat units are wide enough to provide adequate protection from disturbance related to oil and gas development. This assumption remained a key source of uncertainty that could be addressed through additional study of disturbance effects on molting waterfowl.

Alaska↗

USGS1989

Premigrational movements and behavior of young mallards and wood ducks in north-central Minnesota

Movements and behavior of 89 young mallards (Anas platyrhynchos) and 48 young wood ducks (Aix sponsa) were monitored on a 932-km2 study area in north-central Minnesota in late summer and fall, 1972-74, with telemetry, visual observation, and aerial surveys. Initial flights of both species were confined to the natal (brood) marsh; first flights away from the natal marsh occurred in the third week after fledging in both species. First flights of young mallards and wood ducks away from their natal marshes were not significantly different between the sexes (mallard, mean = 4.95 km for females and 5.83 km for males; wood ducks, mean = 2.31 km for females and 2.64 km for males). However, flights away from the brood marshes by wood ducks were significantly shorter than for mallards.As young mallards and wood ducks grew, their daytime use of the natal marshes decreased in an irregular pattern as both species began daily flights between day- and night-use areas. Locally reared mallards made longer daily flights between use areas than did wood ducks, but wood ducks changed use areas with greater frequency before 1 October. Despite often extensive movements, most locally reared mallards and wood ducks remained in the vicinity of their brood marshes throughout fall until migration.Movement of young birds to new habitat was not the result of random searching and thus fortuitous discovery of nearby areas. Instead, birds seemed to learn of new habitat and develop movement patterns by associating with other birds; locally reared young always moved in the company of flocks of conspecifics that included adults and older immatures.Differences in movement patterns between the sexes of young birds and between young and adult birds cause them to be differentially distributed by age and sex on and near the breeding grounds. These differences are ultimately reflected in the distribution of the hunter harvest. We have interpreted generalizations about such phenomena, developed from analysis of continent-wide mallard banding data, using our data obtained from individually marked birds. We document (a) greater distances moved by early than by late-hatched young in the postbreeding period before migration, (b) differential movement of age and sex cohorts that explains greater hunting mortality of young than adults and of females than males near natal marshes, (c) differences in length and timing of postbreeding movements of adult male mallards and the postfledging movements of immature male mallards that help explain the northerly continental recovery distribution of young males, and (d) differential timing and rate of movement by birds through harvest areas (early departure of males and some return of females to natal marshes after the beginning of hunting) that explain differences in the timing of hunting season recoveries. Behavioral differences between the age and sex cohorts in the fall waterfowl population on and near their breeding grounds in north-central Minnesota can explain observed differences in survival and recovery rates of adult and young birds.The behaviors observed suggest to us that restrictive harvest regulations such as small-area closure may have little or no local benefits at the breeding grounds because premigratory assemblages of birds make extensive movements. In particular, protection of postbreeding adult females and locally reared young might only occur by closing large areas or scheduling extreme delays in the season opening, neither of which may be compatible with equitably apportioning waterfowl harvest at higher latitudes. Additional research on the local effects of restrictive regulations, and on age- and sex-specific differences in the timing, rate, and direction of fall movements of postbreeding waterfowl is needed.

Fish and Wildlife Research↗

USGS1972

Techniques for establishing local breeding populations of wood ducks

A study was conducted on the Arrowwood National Wildlife Refuge in east-central North Dakota to further evaluate a technique for establishing nesting wood ducks ( Aix sponsa ) by releasing propagated birds and installing nest houses. No wood duck nesting had been recorded previously in the area. During May-July 1968, 253 ducklings, hand-reared at the Northern Prairie Wildlife Research Center near Jamestown, North Dakota, were released when 9 to 16 days old into a 0.5-acre enclosure on the refuge, where they grew to flight stage and departed. Seventy-eight nest houses were installed in August on the refuge. About 76 percent of the ducks survived until late September, when southward migration began. The first-year band recovery rate by hunters of 4.7 percent was comparable to that of wild immature wood ducks. Most recoveries occurred between North Dakota and Minnesota in the north and Texas and Louisiana in the south. There were 16 nesting attempts, which produced 175 ducklings, by homing female wood ducks in the boxes in 1969. The number of nesting attempts increased to 34 in 1970, with a production of 311 ducklings.

North Dakota↗

USGS2005

Individual variation in staging and timing of spring migration of Pacific common eiders in Alaska

Timing of migration and characterization of migration patterns of birds are usually based on dates of peak migration to and from staging, wintering, and breeding areas used by the bulk of a species. For Pacific common eiders (Somateria mollissima v-nigrum), as well as other species, the timing of migration into and through the Beaufort Sea is based on counts of birds past land or ice-based sites and radar observations, and arrival dates to colonies determined by influxes of birds seen by ground observers. With the continued and proposed development of nearshore and offshore waters of the Beaufort Sea, there is an expanding need to manage local populations. Observations of individual Pacific common eiders can provide a more complete understanding of local populations as well as variability among populations. This study was designed to determine factors influencing migration patterns of individuals nesting in the western Beaufort Sea from their wintering locations along the Chukotka Peninsula, through the eastern Chukchi and western Beaufort seas, until their arrival to their nesting area. The Simpson Lagoon/Maguire Island nesting colonies are 1300-1400 km from the primary winter area. Eiders enter the Beaufort Sea at Point Barrow then move east 300-350 km to their nesting colonies. Nesting adult females were marked with satellite transmitters during summer then followed the next spring and early summer. Transmitters were programmed to provide location data every 3 days (2001, n = 12) or daily (2002 and 2004, n = 7 and 18, respectively) beginning 15 April. I expected the dates of arrival to the colony to vary with weather during migration (Point. Barrow to the colony) and general conditions in spring (early or late year based on differences in temperatures from the long term norm for April, May, and June). All individuals returned to the colony area they were marked the previous year. Data were consistent with other “short” distance migrants. There were no correlations of the dates of arrival to the dates birds left the wintering area, the total days spent staging, wind speed or direction, temperature, weather, or seasonal differences in temperature from the long term average, a plethora of non-significant results. However, two patterns emerged: some birds migrated about 550 km and staged in the eastern Chukchi Sea before migrating to the colonies, while others went directly either to the colony area (1300 km) or elsewhere within the western Beaufort. I will present preliminary analysis and several hypotheses regarding these two strategies.

Alaska↗

USGS2020

“Good” and “bad”: Human perceptions of and interactions with urban wildlife

Urban environments offer habitat for many species of animals. Although some of those are ubiquitous and/or undesirable, others are native and in some cases, of conservation value. In many cases, urban wildlife populations are a source of enjoyment for human residents, who sometimes invest considerable amounts in attracting them to yards and public spaces. Their presence there can serve an important educational role that helps protect non-urban habitats and species. Nonetheless, urban wildlife must survive what has been termed a “landscape of fear.” Although some of the urban wildlife that do well in this environment are benign, other populations – sometimes of a species that, in other locations, is iconic and desirable – can become problematic. Some species can serve as vectors that carry important zoonosis, such as the plague or diseases that affect other wildlife. Others can create noise or olfactory nuisances and degrade structures or usability of public spaces. Some pose hazards at busy airports, whereas still others may present an envenomation or predation risk on unwary humans. Here, we review the role that reptiles, birds, and mammals play in urban environments and discuss how urban wildlife rehabilitation centers help address some related issues. We close by looking ahead and trying to predict how global patterns such as increased urbanization and population growth may affect urban wildlife and its value for conservation.

Book chapter↗

USGS2005

North American Brant: Effects of changes in habitat and climate on population dynamics

We describe the importance of key habitats used by four nesting populations of nearctic brant (Branta bernicla) and discuss the potential relationship between changes in these habitats and population dynamics of brant. Nearctic brant, in contrast to most geese, rely on marine habitats and native intertidal plants during the non-breeding season, particularly the seagrass, Zostera, and the macroalgae, Ulva. Atlantic and Eastern High Arctic brant have experienced the greatest degradation of their winter habitats (northeastern United States and Ireland, respectively) and have also shown the most plasticity in feeding behavior. Black and Western High Arctic brant of the Pacific Flyway are the most dependent on Zostera, and are undergoing a shift in winter distribution that is likely related to climate change and its associated effects on Zostera dynamics. Variation in breeding propensity of Black Brant associated with winter location and climate strongly suggests that food abundance on the wintering grounds directly affects reproductive performance in these geese. In summer, salt marshes, especially those containing Carex and Puccinellia, are key habitats for raising young, while lake shorelines with fine freshwater grasses and sedges are important for molting birds. Availability and abundance of salt marshes has a direct effect on growth and recruitment of goslings and ultimately, plays an important role in regulating size of local brant populations. ?? 2005 Blackwell Publishing Ltd.

Global Change Biology↗