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At least 91 records · Page 5Linked to original sources

Terrestrial wildlife in the post-mined Appalachian landscape: Status and opportunities

Coal mining is an anthropogenic stressor that has impacted terrestrial and semi-aquatic wildlife in the Appalachian Plateau since European settlement. Creation of grassland and early-successional habitats resulting from mining in a forested landscape has resulted in novel, non-analog habitat conditions. Depending on the taxa, the extent of mining on the landscape, and reclamation practices, effects have ranged across a gradient of negative to positive. Forest-obligate species such as woodland salamanders and forest-interior birds or those that depend on aquatic systems in their life cycle have been most impacted. Others, such as grassland and early-successional bird species have responded favorably. Some bat species, as an unintended consequence, use legacy deep mines as winter hibernacula in a region with limited karst geology. Recolonization of impacted wildlife often depends on life strategies and species’ vagility, but also on altered or arrested successional processes on the post-surface mine landscape. Many wildlife species will benefit from Forest Reclamation Approach practices going forward. In the future, managers will be faced with decisions about reforestation versus maintaining open habitats depending on the conservation need of species. Lastly, the post-mined landscape currently is the focal point for a regional effort to restore elk ( Cervus canadensis ) in the Appalachians.

Appalachian Plateau↗

Neuroendocrine and behavioral implications of endocrine disrupting chemicals in quail

Studies in our laboratory have focused on endocrine, neuroendocrine, and behavioral components of reproduction in the Japanese quail. These studies considered various stages in the life cycle, including embryonic development, sexual maturation, adult reproductive function, and aging. A major focus of our research has been the role of neuroendocrine systems that appear to synchronize both endocrine and behavioral responses. These studies provide the basis for our more recent research on the impact of endocrine disrupting chemicals (EDCs) on reproductive function in the Japanese quail. These endocrine active chemicals include pesticides, herbicides, industrial products, and plant phytoestrogens. Many of these chemicals appear to mimic vertebrate steroids, often by interacting with steroid receptors. However, most EDCs have relatively weak biological activity compared to native steroid hormones. Therefore, it becomes important to understand the mode and mechanism of action of classes of these chemicals and sensitive stages in the life history of various species. Precocial birds, such as the Japanese quail, are likely to be sensitive to EDC effects during embryonic development, because sexual differentiation occurs during this period. Accordingly, adult quail may be less impacted by EDC exposure. Because there are a great many data available on normal development and reproductive function in this species, the Japanese quail provides an excellent model for examining the effects of EDCs. Thus, we have begun studies using a Japanese quail model system to study the effects of EDCs on reproductive endocrine and behavioral responses. In this review, we have two goals: first, to provide a summary of reproductive development and sexual differentiation in intact Japanese quail embryos, including ontogenetic patterns in steroid hormones in the embryonic and maturing quail. Second, we discuss some recent data from experiments in our laboratory in which EDCs have been tested in Japanese quail. The Japanese quail provides an excellent avian model for testing EDCs because this species has well-characterized reproductive endocrine and behavioral responses. Considerable research has been conducted in quail in which the effects of embryonic steroid exposure have been studied relative to reproductive behavior. Moreover, developmental processes have been studied extensively and include investigations of the reproductive axis, thyroid system, and stress and immune responses. We have conducted a number of studies, which have considered long-term neuroendocrine consequences as well as behavioral responses to steroids. Some of these studies have specifically tested the effects of embryonic steroid exposure on later reproductive function in a multigenerational context. A multigenerational exposure provides a basis for understanding potential exposure scenarios in the field. In addition, potential routes of exposure to EDCs for avian species are being considered, as well as differential effects due to stage of the life cycle at exposure to an EDC. The studies in our laboratory have used both diet and egg injection as modes of exposure for Japanese quail. In this way, birds were exposed to a specific dose of an EDC at a selected stage in development by injection. Alternatively, dietary exposure appears to be a primary route of exposure; therefore experimental exposure through the diet mimics potential field situations. Thus, experiments should consider a number of aspects of exposure when attempting to replicate field exposures to EDCs.

Hormones and Behavior↗

Host density increases parasite recruitment but decreases host risk in a snail-trematode system

Most species aggregate in local patches. High host density in patches increases contact rate between hosts and parasites, increasing parasite transmission success. At the same time, for environmentally-transmitted parasites, high host density can decrease infection risk to individual hosts, because infective stages are divided among all hosts in a patch, leading to safety in numbers. We tested these predictions using the California horn snail, Cerithideopsis californica (=Cerithidea californica), which is the first intermediate host for at least 19 digenean trematode species in California estuaries. Snails become infected by ingesting trematode eggs or through penetration by free-swimming miracidia that hatch from trematode eggs deposited with final-host (bird or mammal) feces. This complex life cycle decouples infective-stage production from transmission, raising the possibility of an inverse relationship between host density and infection risk. In a field survey, higher snail density was associated with increased trematode (infected snail) density, but decreased trematode prevalence, consistent with either safety in numbers, parasitic castration, or both. To determine the extent to which safety in numbers drove the negative snail density-trematode prevalence association, we manipulated uninfected snail density in 83 cages at eight sites within Carpinteria Salt Marsh (CA, USA). At each site, we quantified snail density and used data on final-host (bird and raccoon) distributions to control for between-site variation in infective-stage supply. After three months, overall trematode infections per cage increased with snail-biomass density. For egg-transmitted trematodes, per-snail infection risk decreased with snail-biomass density in the cage and surrounding area, whereas per-snail infection risk did not decrease for miracidium-transmitted trematodes. Furthermore, both trematode recruitment and infection risk increased with infective-stage input, but this was significant only for miracidium-transmitted species. A model parameterized with our experimental results and snail densities from 524 field transects estimated that safety in numbers, when combined with host aggregation, halved per-capita infection risk in this snail population. We conclude that, depending on transmission mode, host density can enhance parasite recruitment and reduce per-capita infection risk.

Ecology↗

The oral bioavailability and toxicokinetics of methylmercury in common loon ( Gavia immer ) chicks

We compared the toxicokinetics of methylmercury in captive common loon chicks during two time intervals to assess the impact of feather growth on the kinetics of mercury. We also determined the oral bioavailability of methylmercury during these trials to test for age-related changes. The blood concentration-time curves for individuals dosed during feather development (initiated 35 days post hatch) were best described by a one-compartment toxicokinetic model with an elimination half-life of 3 days. The data for birds dosed following completion of feather growth (84 days post hatch) were best fitted by a two-compartment elimination model that includes an initial rapid distribution phase with a half-life of 0.9 days, followed by a slow elimination phase with a half-life of 116 days. We determined the oral bioavailability of methylmercury during the first dosing interval by comparing the ratios of the area under the blood concentration-time curves (AUC 0→∞ ) for orally and intravenously dosed chicks. The oral bioavailability of methylmercury during the first dosing period was 0.83. We also determined bioavailability during both dosing periods using a second measure because of irregularities with intravenous results in the second period. This second bioavailability measure estimated the percentage of the dose that was deposited in the blood volume (f), and the results show that there was no difference in bioavailability among dosing periods. The results of this study highlight the importance of feather growth on the toxicokinetics of methylmercury.

Comparative Biochemistry and Physiology, Part A: M↗

Toxicity of anticholinesterase insecticides to birds: Technical grade versus granular formulations

The acute toxicities of 13 granular anticholinesterase insecticides were compared with their technical grade active ingredients by administering single oral doses of chemical to adult Northern bobwhites (Colinus virginianus) and evaluating resultant LD50 values and dose-response curves. Similar tests with ringed turtledoves (Streptopelia risoria) were conducted with five of the granular formulations to check for interspecific differences. The test chemicals were Amaze 15G (isofenphos), Counter 15G (terbufos), Dasanit 15G (fensulfothion), Diazinon 14G (diazinon), Di-Syston 15G (disulfoton), Dyfonate 20G (fonofos), Furadan 10G (carbofuran), Lorsban 15G (chlorpyrifos), Nemacur 15G (fenamiphos), Parathion 10G (parathion), Tattoo 10G (bendiocarb), Temik 15G (aldicarb), and Thimet 15G (phorate). Information is also presented on dose-response relations and their use in hazard assessment, granule size and hazard, response patterns, and toxic signs. The general conclusions were: (1) The organophosphates (fenamiphos and fensulfothion) and the carbamate (aldicarb) were the most toxic of the insecticides tested. (2) The granular formulation and its technical grade active ingredient were of equivalent toxicity, or the granular was significantly less toxic. (3) The dose-response curve enhances hazard assessment. (4) Ingestion of a single granule of Temik 15G was shown to be life threatening to bobwhite-sized birds, and ingestion of fewer than five granules could be lethal to sparrow-sized birds for Dasanit 15G, Diazinon 14G, Dyfonate 20G, Furadan 15G, and Nemacur 15G. (5) It is therefore suggested that the hazard associated with granular insecticides may be more dependent on which species (cf. size and feeding behavior) inhabit a treated area than on the actual application rate.

Ecotoxicology and Environmental Safety↗

Use of early-successional managed northern forest by mature-forest species during the post-fledging period

In eastern North America, after the young fledge, both adult and juvenile mature-forest birds may use regenerating clearcuts, although which species frequent early-successional forest and during which life stages is not well documented. To assess whether birds nesting in mature forest in north-central Minnesota use regenerating clearcuts 2–10 years old, we netted after birds fledged (2006–2009) and during the breeding season (2009). In addition, we monitored Ovenbird ( Seiurus aurocapilla ) nests and banded nestlings in adjacent mature forest and estimated the age at which juveniles used regenerating clearcuts. While banding, we also recorded nests of any species encountered opportunistically in regenerating clearcuts as evidence of breeding in this cover type. During July and August, we captured 4556 birds of 62 species, of which 1746 (38%) were of 28 mature-forest species. As reported elsewhere, most (76%) mature-forest birds we captured were of only a few species: Ovenbird, American Redstart ( Setophaga ruticilla ), Least Flycatcher ( Empidonax minimus ), and Black-and-white Warbler ( Mniotilta varia ). In 2009, 21% of captures during the nesting period were of mature-forest birds. Comparing dates of fledging from monitored nests to dates of capture in clearcuts implies that nearly all (95%) hatch-year Ovenbirds using clearcuts were independent of adult care. Capture dates of juveniles of other mature-forest species were similar. Although we captured 340 hatch-year Ovenbirds in regenerating clearcuts, we captured only one of 424 Ovenbirds we had banded as nestlings in adjacent mature forest. Within the clearcuts, we encountered nests of five species that typically nest in mature forest.

Minnesota↗

Benefits and costs of increased levels of corticosterone in seabird chicks

Seabird chicks respond to food shortages by increasing corticosterone (cort) secretion, which is probably associated with fitness benefits and costs. To examine this, we experimentally increased levels of circulating cort in captive black-legged kittiwake chicks fed ad libitum. We found that cort-implanted chicks begged more frequently and were more aggressive compared to controls. These behavioral modifications must be beneficial to chicks as they facilitate acquisition of food from the parents and might trigger brood reduction and reduced competition for food. Cort-implanted chicks also increased food intake; however, their growth rates were similar to controls. To examine the costs of chronically increased circulating levels of cort, we removed cort implants and, after a 10-day recovery period, tested cognitive abilities of young kittiwakes. We found that the ability of kittiwakes to associate a visual cue with the presence of food in a choice situation was compromised by the experimental elevation of cort during development. To examine the long-term costs of increased levels of cort, 8 months later we tested the performance of the same individuals in a spatial task requiring them to make a detour around a barrier in order to escape from an enclosure. Individuals treated with cort during development took significantly more time to solve this task compared to controls. The results of this study suggest that the adrenocortical response of a developing bird to environmental stressors is associated with both benefits (increased food intake, foraging behavior, and aggression) and costs (low growth efficiency and compromised cognitive abilities later in life). This provides an evolutionary framework for relating juvenile physiological traits to fitness of birds in subsequent life-history stages. ?? 2003 Elsevier Science (USA). All rights reserved.

Hormones and Behavior↗

Effects of rearing treatment on the behavior of captive whooping cranes (Grus americana)

Small founder populations of whooping cranes are managed to maximize egg production for the purpose of reintroducing young to the wild. This results in an excessive number of hatched chicks that cannot be naturally reared by parents. Hand-rearing techniques have been developed to raise the additional hatches. However, hand rearing may affect the behavior of the birds and their chances of survival later in life. The objectives of this study were to determine the impact of rearing practices on the behavior of whooping crane chicks. The birds were reared under three commonly used rearing techniques: parent reared (PR), hand reared (HR), and hand reared with exercise (HRE). Fifty-six whooping crane chicks were observed by focal animal sampling from hatch to 20 weeks of age. During these observations, occurrences of comfort behavior, aggression, foraging, nonvigilance, sleep, vigilance, and other types of behavior were collected. Data were analyzed using mixed models repeated measures analysis of variance (ANOVA). Behavior was affected by rearing treatment, age, and time of day. PR birds spent more time being vigilant than HR and HRE birds. An inverse correlation was found between percentage of time foraging and vigilant (r = -0.686, P < 0.0001). However, there were no differences in the behavior of birds reared in HR or HRE programs.

Applied Animal Behaviour Science↗

Computer-aided procedure for counting waterfowl on aerial photographs

Examination of 46 Canada goose goslings yielded 14 species of parasites, including five Protozoa, four Nematoda, two Cestoda, and three Trematoda. Evidence indicates that goslings acquired most of these infections during their first week of life. Some parasites, Prosthogonimus sp., occurred only in younger birds. Others, Leucocytozoon simondi, were evident only during the initial course of infection, while still others remained evident in older geese. Parasites with a direct life cycle appeared to be more prevalent than those requiring intermediate hosts. Among 29 birds from a refuge in Michigan, 14 species of parasites were found; while in 17 goslings from a Utah refuge, only five species occurred.

Wildlife Society Bulletin↗

Seasonality of biological and physical systems as indicators of climatic variation and change

Evidence-based responses to climate change by society require operational and sustained information including biophysical indicator systems that provide up-to-date measures of trends and patterns against historical baselines. Two key components linking anthropogenic climate change to impacts on socio-ecological systems are the periodic inter- and intra-annual variations in physical climate systems (seasonality) and in plant and animal life cycles (phenology). We describe a set of national indicators that reflect sub-seasonal to seasonal drivers and responses of terrestrial physical and biological systems to climate change and variability at the national scale. Proposed indicators and metrics include seasonality of surface climate conditions (e.g., frost and freeze dates and durations), seasonality of freeze/thaw in freshwater systems (e.g., timing of stream runoff and durations of lake/river ice), seasonality in ecosystem disturbances (e.g., wildfire season timing and duration), seasonality in vegetated land surfaces (e.g., green-up and brown-down of landscapes), and seasonality of organismal life-history stages (e.g., timings of bird migration). Recommended indicators have strong linkages to variable and changing climates, include abiotic and biotic responses and feedback mechanisms, and are sufficiently simple to facilitate communication to broad audiences and stakeholders interested in understanding and adapting to climate change.

Climatic Change↗

A potential predator-prey interaction of an American badger and an Agassiz's desert tortoise with a review of badger predation on turtles

The federally threatened Agassiz’s desert tortoise ( Gopherus agassizii ) was listed under the U.S. Endangered Species Act in 1990, but thus far, recovery efforts have been unsuccessful (U.S. Fish and Wildlife Service [USFWS] 2015). Predation has been identified as a contributing factor to declining G. agassizii populations range-wide (e.g., Esque et al. 2010, Lovich et al. 2014). Understanding and managing for predator-prey dynamics is thus an important part of the recovery and conservation of this threatened species (USFWS 2011). Desert tortoises have a host of predators at all stages of their life cycle. Over 20 species of birds, mammals, and reptiles have been recorded as known or suspected predators (Woodbury and Hardy 1948, Luckenbach 1982, Ernst and Lovich 2009). American badgers ( Taxidea taxus , family: Mustelidae) are confirmed excavators of desert tortoise nests (Turner and Berry 1984). They are also suspected predators of adult desert tortoises, a possibility which has been presented in some studies but without empirical verification (Luckenbach 1982, Turner and Berry 1984). Active mostly at night, badgers are solitary, secretive predators (Lindzey 1978, 1982; Armitage 2004) that are extremely difficult to observe in predatory encounters. Recently, strong circumstantial evidence presented by Emblidge et al. (2015) suggests that badgers do prey on adult Agassiz’s desert tortoises based on observations of more than two dozen dead tortoises in the Western Mojave Desert of California. In this note, we present another case of potential badger predation on a large adult desert tortoise in the Sonoran Desert of California. Collectively, these recent two cases potentially indicate that badger predation may be more common and widespread than previously thought. In addition, we review the worldwide literature of badger predation on turtles in general and summarize reported badger observations in Joshua Tree National Park, where our observation occurred, over a period of 55 years.

California↗

Movements of immature bald eagles: Implications for bird aircraft strike hazard

Bald eagle (Haliaeetus leucocephalus) aircraft strikes have increased dramatically over the last 20 years as their populations have recovered to near historic sizes. Their attraction to airfields and their large body size makes them a danger to aircraft and therefore important to airfield wildlife managers. However, their management is complicated by their special protected status and the iconic place they hold in the eyes of the public. To help airfield wildlife managers plan monitoring efforts and make informed management decisions, we studied the movements of 32 bald eagles telemetered as nestlings in the Chesapeake Bay of Virginia, USA. Managers often need to know when fledged eagles are most likely to move enough to encounter airfields near nests. As fledglings aged they moved progressively farther from the nest and spent more time away from the nest. Twenty-eight days after fledging, eagles spent most of the day (81±10%, 95% confidence interval) near the nest (<500 m) and only 7±7% of the daytime away from the nest (>1 km). By day 53 fledglings ventured beyond 2.5 km from the nest and spent 30 ± 15% the day >1 km away from their nest. However, distances moved were influenced by proximity of the nest to water, the quality and salinity of that water, and human population density. Eagles left their natal areas and generally migrated out of the Chesapeake Bay 60.5 ± 7.7 days (4 August) after fledging and returned to the Chesapeake Bay approximately 225 days later (March-April). Eighty-four percent (27 of 32) of the eagles that we tracked encountered 164 airfields across the east coast with 91% of those airfields located within 10 km of the Chesapeake Bay. Encounters with airfields outside the Chesapeake Bay occurred mainly during the first 1.5 years of life, peaking in late fall and early spring. Eagles were recorded on Chesapeake Bay airfields during each year, but encounters peaked in April of the first year of the bird’s life. This month coincides with the height of reported strikes of eagles by aircraft in the region. Our results suggest that eagles fledging from the Chesapeake Bay are not only an issue for airports near the Chesapeake Bay, but for airports across the east coast. Given the continued growth of the population, this issue is likely to continue and grow in significance.

Virginia↗

The relationship between annual survival rate and migration distance in mallards: An examination of the time-allocation hypothesis for the evolution of migration

Predictions of the time-allocation hypothesis were tested with several a posteriori analyses of banding data for the mallard (Anas platyrhynchos). The time-allocation hypothesis states that the critical difference between resident and migrant birds is their allocation of time to reproduction on the breeding grounds and survival on the nonbreeding grounds. Residents have higher reproduction and migrants have higher survival. Survival and recovery rates were estimated by standard band-recovery methods for banding reference areas in the central United States and central Canada. A production-rate index was computed for each reference area with data from the U.S. Fish and Wildlife Service May Breeding Population Survey and July Production Survey. An analysis of covariance was used to test for the effects of migration distance and time period (decade) on survival, recovery, and production rates. Differences in migration chronology were tested by comparing direct-recovery distributions for different populations during the fall migration. Differences in winter locations were tested by comparing distributions of direct recoveries reported during December and January. A strong positive relationship was found between survival rate, and migration distance for 3 of the 4 age and sex classes. A weak negative relationship was found between recovery rate and migration distance. No relationship was found between production rate and migration distance. During the fall migration, birds from the northern breeding populations were located north of birds from the southern breeding populations. No pattern could be found in the relative locations of breeding and wintering areas. Although our finding that survival rate increased with migration distance was consistent with the time-allocation hypothesis, our results on migration chronology and location of wintering areas were not consistent with the mechanism underlying the time-allocation hypothesis. Neither this analysis nor other recent studies of life-history characteristics of migratory and resident birds supported the timeallocation hypothesis.

Canadian Journal of Zoology↗

Book review: Bird census techniques, Second edition

Conservation concerns, federal mandates to monitor birds, and citizen science programs have spawned a variety of surveys that collect information on bird populations. Unfortunately, all too frequently these surveys are poorly designed and use inappropriate counting methods. Some of the flawed approaches reflect a lack of understanding of statistical design; many ornithologists simply are not aware that many of our most entrenched counting methods (such as point counts) cannot appropriately be used in studies that compare densities of birds over space and time. It is likely that most of the readers of The Condor have participated in a bird population survey that has been criticized for poor sampling methods. For example, North American readers may be surprised to read in Bird Census Techniques that the North American Breeding Bird Survey 'is seriously flawed in its design,' and that 'Analysis of trends is impossible from points that are positioned along roads' (p. 109). Our conservation efforts are at risk if we do not acknowledge these concerns and improve our survey designs. Other surveys suffer from a lack of focus. In Bird Census Techniques, the authors emphasize that all surveys require clear statements of objectives and an understanding of appropriate survey designs to meet their objectives. Too often, we view survey design as the realm of ornithologists who know the life histories and logistical issues relevant to counting birds. This view reflects pure hubris: survey design is a collaboration between ornithologists, statisticians, and managers, in which goals based on management needs are met by applying statistical principles for design to the biological context of the species of interest. Poor survey design is often due to exclusion of some of these partners from survey development. Because ornithologists are too frequently unaware of these issues, books such as Bird Census Techniques take on added importance as manuals for educating ornithologists about the relevance of survey design and methods and the often subtle interdisciplinary nature of surveys. Review info: Bird Census Techniques, Second Edition. By Colin J. Bibby, Neil D. Burgess, David A. Hill, and Simon H. Mustoe. 2000. Academic Press, London, UK. xvii 1 302 pp. ISBN 0- 12-095831-7.

Condor↗

Comparison of immune responses of brown-headed cowbird and related blackbirds to West Nile and other mosquito-borne encephalitis viruses

The rapid geographic spread of West Nile virus (family Flaviviridae , genus Flavivirus , WNV) across the United States has stimulated interest in comparative host infection studies to delineate competent avian hosts critical for viral amplification. We compared the host competence of four taxonomically related blackbird species (Icteridae) after experimental infection with WNV and with two endemic, mosquito-borne encephalitis viruses, western equine encephalomyelitis virus (family Togaviridae , genus Alphavirus , WEEV), and St, Louis encephalitis virus (family Flaviviridae , genus Flavivirus , SLEV). We predicted differences in disease resistance among the blackbird species based on differences in life history, because they differ in geographic range and life history traits that include mating and breeding systems. Differences were observed among the response of these hosts to all three viruses, Red-winged Blackbirds were more susceptible to SLEV than Brewer's Blackbirds, whereas Brewer's Blackbirds were more susceptible to WEEV than Red-winged Blackbirds. In response to WNV infection, cowbirds showed the lowest mean viremias, cleared their infections faster, and showed lower antibody levels than concurrently infected species. Brown-headed Cowbirds also exhibited significantly lower viremia responses after infection with SLEV and WEEV as well as coinfection with WEEV and WNV than concurrently infected icterids. We concluded that cowbirds may be more resistant to infection to both native and introduced viruses because they experience heightened exposure to a variety of pathogens of parenting birds during the course of their parasitic life style.

Journal of Wildlife Diseases↗

Avian tick paralysis caused by Ixodes brunneus in the southeastern United States

Between 1988 and 1994, 16 definitive and 26 presumptive cases of tick paralysis were diagnosed in 10 species of birds from five southeastern states in the USA. All birds had engorged adult female Ixodes brunneus ticks on the head region and were partially paralyzed or dead. Cases occurred in the winter and early spring months, and most birds were passerines found in private yards or near feeders. All stages of I. brunneus feed exclusively on birds, and this species previously has been associated with avian tick paralysis. Little is known concerning the life cycle of this ixodid tick and its impact on wild bird populations.

Journal of Wildlife Diseases↗

Bird migration patterns in the arid southwest-Final report

To ensure full life-cycle conservation, we need to understand migrant behavior en route and how migrating species use stopover and migration aerohabitats. In the Southwest, birds traverse arid and mountainous landscapes in migration. Migrants are known to use riparian stopover habitats; we know less about how migrant density varies across the Southwest seasonally and annually, and how migrants use other habitat types during migratory stopover. Furthermore, we lack information about migrant flight altitudes, speeds, and directions of travel, and how these patterns vary seasonally and annually across the Southwest. Using weather surveillance radar data, we identified targets likely dominated by nocturnally migrating birds and determined their flight altitudes, speeds, directions over ground, and variations in abundance. Migrating or foraging bats likely are present across the region in some of these data, particularly in central Texas. We found that migrants flew at significantly lower altitudes and significantly higher speeds in spring than in fall. In all seasons migrants maintained seasonally appropriate directions of movement. We detected significant differences in vertical structure of migrant densities that varied both geographically within seasons and seasonally within sites. We also found that in fall there was a greater and more variable passage of migrants through the central part of the borderlands (New Mexico and west Texas); in spring there was some suggestion of greater and more variable passage of migrants in the eastern borderlands (central and south Texas). Such patterns are consistent with the existence of at least two migration systems through western North America and the use of different migration routes in spring and fall for at least some species. Using radar data and satellite land cover data, we determined the habitats with which migrants are associated during migration stopover. There were significant differences in bird densities among habitat types at all sites in at least one season. Upland forest habitat in parts of Arizona and New Mexico supported high migrant densities, especially in fall. Developed habitats in areas with little upland forest habitat also supported high migrant densities. Scrub/shrub and grassland habitats supported low to intermediate migrant densities, but because these habitat types dominate the region, they may support large numbers of migratory birds. This may be especially true for species that do not use forested habitats during migration. Target identity remains a challenge for radar-based studies. Presence of bats in the data complicates interpretation of some observations, particularly from central Texas. Based on our results it is simplistic to: (1) consider the arid west as a largely inhospitable landscape in which there are only relatively small oases of habitat that provide the resources needed by all migrants; (2) think of western riparian and upland forest habitat as supporting the majority of migrants in all cases; or (3) consider a particular habitat type unimportant migrant stopover habitat based solely on migrant densities.

Open-File Report↗

Large-scale range collapse of Hawaiian forest birds under climate change and the need 21st century conservation options

Hawaiian forest birds serve as an ideal group to explore the extent of climate change impacts on at-risk species. Avian malaria constrains many remaining Hawaiian forest bird species to high elevations where temperatures are too cool for malaria's life cycle and its principal mosquito vector. The impact of climate change on Hawaiian forest birds has been a recent focus of Hawaiian conservation biology, and has centered on the links between climate and avian malaria. To elucidate the differential impacts of projected climate shifts on species with known varying niches, disease resistance and tolerance, we use a comprehensive database of species sightings, regional climate projections and ensemble distribution models to project distribution shifts for all Hawaiian forest bird species. We illustrate that, under a likely scenario of continued disease-driven distribution limitation, all 10 species with highly reliable models (mostly narrow-ranged, single-island endemics) are expected to lose >50% of their range by 2100. Of those, three are expected to lose all range and three others are expected to lose >90% of their range. Projected range loss was smaller for several of the more widespread species; however improved data and models are necessary to refine future projections. Like other at-risk species, Hawaiian forest birds have specific habitat requirements that limit the possibility of range expansion for most species, as projected expansion is frequently in areas where forest habitat is presently not available (such as recent lava flows). Given the large projected range losses for all species, protecting high elevation forest alone is not an adequate long-term strategy for many species under climate change. We describe the types of additional conservation actions practitioners will likely need to consider, while providing results to help with such considerations.

Hawaii↗