Search USGS⌕ Search

Geology topics

David A. Buehler

Publications and source records attributed to David A. Buehler.

At least 19 recordsLinked to original sources

Northern bobwhites select for native grasses on working grazing land

Northern bobwhite ( Colinus virginianus ; bobwhite) populations have experienced an 85% decline across most of its range since the 1960s. The most drastic decreases have been in the southeastern United States where biologists attribute the decline to widespread habitat loss, including conversion of native grasslands to tall fescue ( Lolium arundinaceum ) and other exotic cool-season grass (CSG) pasture and hayfields. Including agricultural lands in conservation programs could improve habitat conditions on a regional scale. One working-lands conservation strategy involves the use of native warm-season grasses (NWSGs) rather than cool-season exotic grasses as economically viable cattle forage. To evaluate this management practice for creating bobwhite habitat, we conducted a field study on a bobwhite population in eastern Kentucky, USA, where grazed NWSG and burned NWSG fields were adjacent to exotic grazed and exotic hayed CSG fields. Between April 2019 and October 2022, we used radio telemetry to track bobwhites to evaluate resource selection at second- and third-order scales. Bobwhites used traditionally managed CSGs less than would be expected by chance at the second-order scale in both breeding and non-breeding seasons. Bobwhite use of grazed NWSG and burned NWSG was greater than would be expected by chance at the second-order scale in both breeding and non-breeding seasons. Similarly, at the third-order scale, bobwhites used CSGs less than would be expected by chance, whereas NWSGs and woody stems were used more than by chance alone. Our study suggests that bobwhites select NWSGs at multiple spatial scales despite broad-scale availability of managed exotic CSGs. Under a working-lands framework, the integration of NWSGs into working lands could create bobwhite habitat in the southeastern United States, especially if woody stems are present.

Kentucky↗

Comparison of methods for estimating wild turkey poult survival

Eastern wild turkey ( Meleagris gallopavo silvestris ) population growth is driven by variation in reproduction, and poult survival is a crucial vital rate. Traditional poult survival monitoring uses flush counts of radio-tagged females, but brood flocking (when broods and females merge into larger flocks) and mark retention are potential problems with this method and can produce biased estimates. Alternatively, radio-tagging poults to estimate survival offers a potentially less-biased method if tagging and tracking poults can be conducted without adverse effects on the poults. We compared poult survival estimates derived from flush counts and from radio-tagged poults over a 56-day monitoring period during 2018–2022 in south-central Tennessee, USA. We radio-tagged 183 poults and monitored 85 broods via 2-week flush counts and observed 572 individual poults during flush counts over the 56-day monitoring period. We used known-fate survival models for the telemetry data, Lukacs survival models for the flush count data, and a modified known-fate model to estimate whether radio-tagging poults affected their survival. Two-week survival estimates from the flush count of broods, and radio-tagged poults were similar (flush count: day 0–28: 0.25, 95% CI: 0.20–0.31, day 29–56: 0.56, 95% CI: 0.36–0.76; radio-tagged: day 0–28: 0.30, 95% CI: 0.23–0.37, day 29–56: 0.68, 95% CI: 0.49–0.87). Using known-fate survival models, radio-tagged poults had similar survival rates to non-tagged poults within the brood (day 0–28: Ŝ Radio-tagged = 0.15, 95% CI: 0.10–0.20 v. Ŝ Non-tagged = 0.20, 95% CI: 0.16–0.23), which suggests the radio-tags did not directly affect survival. However, survival of individuals that were trapped was lower than survival of broods that were not trapped during the first 14 days. Trapping methods may need to be adjusted to limit incidental capture effects when choosing to use radio-tagged poults. Conducting flush counts every 14 days until day 56 of the brood-rearing period likely is the most cost-effective method for estimating poult survival. However, monitoring individual radio-tagged poults may yield additional information, such as cause-specific mortality, that may better inform management.

Tennessee↗

Apparent annual survival of adult Golden-winged Warblers (Vermivora chrysoptera) may not differ by sex or region

Understanding range-wide demographic, spatial, and temporal variation in annual survival is essential for managing species of conservation concern. Multi-population models are useful tools for integrating diverse datasets, reducing biases, and deriving survival estimates across differing spatial scales. We conducted a range-wide, multi-population apparent annual survival analysis for a declining songbird, Vermivora chrysoptera (Golden-winged Warbler), using data from 18 sites across its breeding and nonbreeding grounds. This Nearctic-Neotropical migrant breeds in 2 disjunct regional populations, the Great Lakes and Appalachian Mountains, which are experiencing different rates of decline. We aimed to quantify regional-, site-, and sex-specific apparent annual survival estimates to identify geographic patterns or demographic factors influencing population declines. We used simulations to assess the precision of our estimates. Our models did not reveal a substantial difference in apparent annual survival between the Great Lakes (0.41, 95% credible interval (CrI):0.31–0.50) and the Appalachian regions (0.49, 95% CrI: 0.36–0.60), as CrIs overlapped. Site-specific estimates also showed no clear differences in apparent annual survival among sites representing both regional populations. Male apparent annual survival tended to be greater than female apparent annual survival in both regions, though CrI’s overlapped. Our study suggests demographic factors other than adult annual survival likely play a larger role in recent regional and range-wide population declines, such as productivity, juvenile/immature survival, or recruitment. Simulations indicate that improving recapture probability and study duration of datasets could lead to more precise apparent annual survival estimates. However, our model produced CrI ranges comparable to the most ideal data collection scenario, suggesting the lack of trends we found was not due to variability in our estimates. We stress the importance of addressing inherent biases in survival datasets and the need for standardized collaborative efforts to inform species conservation on a range-wide scale.

Ornithology↗

Assessing wild turkey productivity before and after a 14-day delay in the start date of the spring hunting season in Tennessee

Ten state wildlife management agencies in the United States, including six within the Southeast, have delayed their spring wild turkey ( Meleagris gallopavo ) hunting seasons since 2017 by five or more days to address concerns related to the potential effects of hunting on wild turkey seasonal productivity. One hypothesis posits that if the spring hunting season is too early, there may be insufficient time for males to breed hens before being harvested, thus leading to reduced seasonal productivity. We conducted an experiment to determine whether delaying the wild turkey hunting season by 2 weeks in south-middle Tennessee would affect various reproductive rates. In 2021 and 2022, the Tennessee Fish and Wildlife Commission experimentally delayed the spring hunting season to open 14 days later than the traditional date (the Saturday closest to 1 April) in Giles, Lawrence, and Wayne counties. We monitored reproductive rates from 2017 to 2022 in these three counties as well as two adjacent counties, Bedford and Maury, that were not delayed. We used a Before-After-Control-Impact design to analyze the proportion of hens nesting, clutch size, hatchability, nest success, poult survival and hen survival with linear mixed-effect models and AIC model selection to detect relationships between the 14-day delay and reproductive parameters. We detected no relationship ( p > .05) between the 14-day delay and any individual reproductive parameter. In addition, recruitment (hen poults per hen that survived until the next breeding season) was very low (<0.5) and did not increase because of the 14-day delay. The traditional Tennessee start date had been in place since 1986 while the turkey harvest increased markedly until about 2006 and more recently stabilized. Our data indicate that moving the start of the hunting season from a period just prior to peak nest initiation to 2 weeks later, to coincide with a period just prior to peak nest incubation initiation, resulted in no change to productivity or populations in wild turkey flocks in south-middle Tennessee.

Tennessee↗

Exposure to risk factors experienced during migration is not associated with recent Vermivora warbler population trends

Context Understanding the factors limiting populations of animals is critical for effective conservation. Determining which factors limit populations of migratory species can be especially challenging because of their reliance on multiple, often geographically distant regions during their annual cycles. Objectives We investigated whether distribution-wide variation in recent breeding population trends was more strongly associated with exposure to risk factors experienced during migration (i.e., natural and anthropogenic threats often associated with increased mortality or carry-over effects) or factors associated with breeding and nonbreeding areas in golden-winged warblers ( Vermivora chrysoptera ) and blue-winged warblers ( V. cyanoptera ), two Nearctic-Neotropical migrants experiencing regionally variable population trends. Methods We used geolocator data from 85 Vermivora warblers ( n = 90 geolocator tracks) tracked from North American breeding locations and Central American nonbreeding locations from 2013 to 2017 to determine variation in space use among populations. We assessed whether differences in space use among populations of Vermivora warblers during migration were associated with exposure to migration risk-factors and whether increased relative exposure to migration risk factors was associated with population declines at regional and subregional scales. Results Regional and subregional populations of Vermivora warblers exhibited variation in space use and exposure to anthropogenic and natural risk-factors. However, we found no evidence that recent variation in population trends of Vermivora warblers was associated with risk-factors experienced by different populations during migration. Instead, factors associated with land cover-types in breeding and nonbreeding areas were more strongly associated with recent population trends. Conclusions Understanding how populations of migratory birds are affected by factors experienced during migration is critical for their conservation. We did not find evidence that variation in exposure to migration risk-factors is associated with recent regional or subregional variation in Vermivora warbler population trends. Consequently, our results suggest that efforts to reverse ongoing population declines of Vermivora warblers may be more effective if directed toward conservation actions targeting limiting factors within the breeding and nonbreeding periods versus those directed at conditions encountered during migration. We caution that geographic variation in projected land-use change may differentially affect areas used by different populations of Vermivora warblers during migration, posing a potential threat to these species in the future.

Landscape Ecology↗

Change in climatically suitable breeding distributions reduces hybridization potential between Vermivora warblers

Aim Climate change is affecting the distribution of species and subsequent biotic interactions, including hybridization potential. The imperiled Golden-winged Warbler (GWWA) competes and hybridizes with the Blue-winged Warbler (BWWA), which may threaten the persistence of GWWA due to introgression. We examined how climate change is likely to alter the breeding distributions and potential for hybridization between GWWA and BWWA. Location North America. Methods We used GWWA and BWWA occurrence data to model climatically suitable conditions under historical and future climate scenarios. Models were parameterized with 13 bioclimatic variables and 3 topographic variables. Using ensemble modeling, we estimated historical and modern distributions, as well as a projected distribution under six future climate scenarios. We quantified breeding distribution area, the position of and amount of overlap between GWWA and BWWA distributions under each climate scenario. We summarized the top explanatory variables in our model to predict environmental parameters of the distributions under future climate scenarios relative to historical climate. Results GWWA and BWWA distributions are projected to substantially change under future climate scenarios. GWWA are projected to undergo the greatest change; the area of climatically suitable breeding season conditions is expected to shift north to northwest; and range contraction is predicted in five out of six future climate scenarios. Climatically suitable conditions for BWWA decreased in four of the six future climate scenarios, while the distribution is projected to shift east. A reduction in overlapping distributions for GWWA and BWWA is projected under all six future climate scenarios. Main Conclusions Climate change is expected to substantially alter the area of climatically suitable conditions for GWWA and BWWA, with the southern portion of the current breeding ranges likely to become climatically unsuitable. However, interactions between BWWA and GWWA are expected to decline with the decrease in overlapping habitat, which may reduce the risk of genetic introgression.

Diversity and Distributions↗

Population trends in Vermivora warblers are linked to strong migratory connectivity

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

Proceedings of the National Academy of Sciences of↗

Response to Lisovski et al.

Lisovski et al. [1] describe the widely recognized limitations of light-level geolocator data for identifying short-distance latitudinal movements, recommend that caution be used when interpreting such data, intimated that we did not use such caution and argued that environmental shading likely explained the Golden-winged Warbler ( Vermivora chrysoptera ) movements described in our 2015 report [2] . Lisovski et al. [1] conclude that the bird movements we reported could not be disentangled from estimation error in stationary animals caused by environmental shading. We argue that, to the contrary, these hypotheses can easily be disentangled because the premise that environmental shading caused synchronous and parallel error among geolocators is false. With their assertion that our location estimates could be biased by >3,500 km on a day with no observable local sources of shading, Lisovski et al. [1] have taken a position of incredulity toward all geolocator-based animal movement data published to date.

Current Biology↗

An evaluation and comparison of conservation guidelines for an at-risk migratory songbird

For at-risk wildlife species, it is important to consider conservation within the process of adaptive management. Golden-winged Warblers (Vermivora chrysoptera) are Neotropical migratory songbirds that are experiencing long-term population declines due in part to the loss of early-successional nesting habitat. Recently-developed Golden-winged Warbler habitat management guidelines are being implemented by USDA: Natural Resource Conservation Service (2014) and its partners through the Working Lands For Wildlife (WLFW) program. During 2012–2014, we studied the nesting ecology of Golden-winged Warblers in managed habitats of the eastern US that conformed to WLFW conservation practices. We evaluated five NRCS “management scenarios” with respect to nesting success and attainment of recommended nest site vegetation conditions outlined in the Golden-winged Warbler breeding habitat guidelines. Using estimates of territory density, pairing rate, nest survival, and clutch size, we also estimated fledgling productivity (number of fledglings/ha) for each management scenario. In general, Golden-winged Warbler nest survival declined as each breeding season advanced, but nest survival was similar across management scenarios. Within each management scenario, vegetation variables had little influence on nest survival. Still, percent Rubus cover and density of >2 m tall shrubs were relevant in some management scenarios. All five management scenarios rarely attained recommended levels of nest site vegetation conditions for Golden-winged, yet nest survival was high. Fledgling productivity estimates for each management scenario ranged from 2.1 to 8.6 fledglings/10 hectares. Our results indicate that targeted habitat management for Golden-winged Warblers using a variety of management techniques on private lands has the capability to yield high nest survival and fledgling productivity, and thus have the potential to contribute to the species recovery.

Global Ecology and Conservation↗

Nonbreeding isolation and population-specific migration patterns among three populations of Golden-winged Warblers

Golden-winged Warblers ( Vermivora chrysoptera ) are Nearctic–Neotropical migrants experiencing varied regional population trends not fully explained by breeding-grounds factors such as nest success. A lack of detailed information on the nonbreeding distributions, migration routes, or timing of migration among populations hampers our ability to identify population processes outside the breeding period. We used geolocators to track annual movements of 21 Golden-winged Warblers from 3 North American breeding locations experiencing varying population trends to investigate the potential for nonbreeding site factors to influence breeding populations. We used the template-fit method to estimate locations of individual warblers throughout the year. Geolocator-marked warblers exhibited significant isolation among populations during migration and the nonbreeding period. During the nonbreeding period, Golden-winged Warblers from Minnesota, USA ( n = 12) occurred in Central America from southern Mexico to central Nicaragua; warblers from Tennessee, USA ( n = 7) occurred along the border of northern Colombia and Venezuela; and warblers from Pennsylvania, USA ( n = 2) occurred in north-central Venezuela. Warblers travelled at slower rates over more days in fall migration than spring migration. Fall migration routes at the Gulf of Mexico were population-specific, whereas spring routes were more varied and overlapped among populations. Golden-winged Warblers from Pennsylvania migrated 4,000 and 5,000 km yr −1 farther than Tennessee and Minnesota warblers, respectively, and spent almost twice as long migrating in the fall compared to Minnesota warblers. Our results reveal nearly complete temporal and geographic isolation among 3 populations of Golden-winged Warblers throughout the annual cycle, resulting in opportunities for population- and site-specific factors to differentially influence populations outside the breeding period. Our findings highlight the need for monitoring multiple populations of migratory species to understand and better inform conservation strategies.

Condor↗

Dynamic distributions and population declines of Golden-winged Warblers

With an estimated breeding population in 2010 of 383,000 pairs, the Golden-winged Warbler ( Vermivora chrysoptera ) is among the most vulnerable and steeply declining of North American passerines. This species also has exhibited among the most dynamic breeding distributions, with populations expanding and then contracting over the past 150 years in response to regional habitat changes, interactions with closely related Blue-winged Warblers ( V. cyanoptera ), and possibly climate change. Since 1966, the rangewide population has declined by >70% (-2.3% per year; latest North American Breeding Bird Survey data), with much steeper declines in the Appalachian Mountains bird conservation region (-8.3% per year, 98% overall decline). Despite apparently stable or increasing populations in the northwestern part of the range (Minnesota, Manitoba), population estimates for Golden-winged Warbler have continued to decline by 18% from the decade of the 1990s to the 2000s. Population modeling predicts a further decline to roughly 37,000 individuals by 2100, with the species likely to persist only in Manitoba, Minnesota, and possibly Ontario. To delineate the present-day distribution and to identify population concentrations that could serve as conservation focus areas, we compiled rangewide survey data collected in 2000-2006 in 21 states and 3 Canadian provinces, as part of the Golden-winged Warbler Atlas Project (GOWAP), supplemented by state and provincial Breeding Bird Atlas data and more recent observations in eBird. Based on >8,000 GOWAP surveys for Golden-winged and Blue-winged warblers and their hybrids, we mapped occurrence of phenotypically pure and mixed populations in a roughly 0.5-degree grid across the species’ ranges. Hybrids and mixed Golden-winged-Blue-winged populations occurred in a relatively narrow zone across Minnesota, Wisconsin, Michigan, southern Ontario, and northern New York. Phenotypically pure Golden-winged Warbler populations occurred north of this hybrid zone, but the future of northern populations in the Great Lakes states and Canada (where >80% of the species occurs at present) is highly uncertain because of continued northward expansion of Blue-winged Warblers and hybridization. A second, now-disjunct band of Golden-winged Warbler populations exists in the Appalachian Mountains from southeastern New York to northern Georgia, surrounded at lower elevations by Blue-winged Warblers. Important concentrations of Golden-winged Warblers persist in the Allegheny Mountains region of West Virginia, the Cumberland Mountains in Tennessee, Blue Ridge Mountains of western North Carolina, Allegheny Plateau and Pocono Mountains in Pennsylvania, and in the Hudson Highlands of southern New York. These high-elevation Appalachian populations have escaped contact with Blue-winged Warblers until very recently and represent important refugia for conservation and management; other Appalachian populations are rapidly declining. In addition, based on historical records and standardized surveys across the wintering grounds, we identified three regions of concentration: highlands and Caribbean slopes from Guatemala and Belize to northwestern Nicaragua; middle elevations (both slopes) in Costa Rica and western Panama; and in an arc of the northern Andes from central Colombia to northern Venezuela. It is possible that the winter range has been shifting towards the northwest in recent decades, paralleling shifts in the breeding distribution. Future conservation efforts for Golden-winged Warbler need to include close monitoring of the dynamic phenotypic and genetic distributional shifts, and may need to consider the “winged warbler” complex together as a highly adaptable evolutionary unit.

Studies in Avian Biology↗

Golden-winged Warbler nest-site habitat selection: Chapter 7

Avian habitat selection occurs at multiple spatial scales to incorporate life history requirements. Breeding habitat of Golden-winged Warblers ( Vermivora chrysoptera ) is characterized by largely forested landscapes containing natural or anthropogenic disturbance elements that maintain forest patches in early stages of succession. Breeding habitat occurs in a variety of settings, including shrub and forest swamps, regenerating forests following timber harvest, grazed pastures, and reclaimed mined lands. We identified structural components of nest sites for Golden-winged Warblers by measuring habitat characteristics across five states (North Carolina, New York, Pennsylvania, Tennessee, and West Virginia) in the Appalachian breeding-distribution segment and two states (Minnesota and Wisconsin) in the Great Lakes breeding-distribution segment. We measured habitat characteristics at the nest-site scale with a series of nested plots characterizing herbaceous vegetation (grasses and forbs), woody shrubs and saplings, and overstory trees. We measured similar variables at paired random plots located 25–50 m from the nest within the same territory to evaluate selection. We used conditional logistical regression to identify which parameters were important in habitat selection and Simple Saddlepoint Approximation (SSA) to aid in management interpretation of identified parameters for each study site. Study site was an important determinant for which parameters were significant in nest-site selection, although selection for some parameters was consistent across sites. The amount of woody cover at the nest-site scale was consistently present in the top nest-site selection models across sites, although the direction of the relationship was not the same across all sites. We also identified grass, forb, woody cover, and vegetation density as important components of Golden-winged Warbler nest-site selection. Based on SSA, we identified vegetation thresholds to aid in designing habitat management prescriptions to promote creation or restoration of Golden-winged Warbler nesting habitat across the eastern portion of their breeding distribution.

Studies in Avian Biology↗

Research on Golden-winged Warblers: Recent progress and current needs

Considerable advances have been made in knowledge about Golden-winged Warblers ( Vermivora chrysoptera ) in the past decade. Recent employment of molecular analysis, stable-isotope analysis, telemetry-based monitoring of survival and behavior, and spatially explicit modeling techniques have added to, and revised, an already broad base of published knowledge. Here, we synthesize findings primarily from recent peer-reviewed literature on Golden-winged Warblers, from this volume and elsewhere, and we identify some of the substantial remaining research needs. We have organized this synthesis by stages of the Golden-winged Warbler annual cycle. First, we discuss the relatively well-studied breeding-grounds ecology including nesting and post-fledging ecology and hybridization with closely related Blue-winged Warblers ( Vermivora cyanoptera ). Second, we discuss the much-less-studied, non-breeding-grounds ecology, including the first empirical studies of non-breeding-grounds cover-type associations and spatial and social behavioral ecology. Third, we address migratory connectivity and migration ecology, for which little is known and research has only just begun. Last, we close with cautious optimism that current knowledge is adequate to inform initial conservation and management plans for Golden-winged Warblers, and with a sobering acknowledgement of the quantity of research still needed.

Studies in Avian Biology↗

Habitat quality from individual- and population-level perspectives and implications for management

Many wildlife management prescriptions are either implicitly or explicitly designed to improve habitat quality for a focal species, but habitat quality is often difficult to quantify. Depending upon the approach used to define and identify high-quality habitat, management decisions may differ widely. Although individual-level measures of habitat quality based on per capita reproduction (e.g., average nesting success, number of young produced per pair) are most common in the literature, they may not align with population-level measures that reflect number of young produced within a defined area. Using data on the cerulean warbler ( Setophaga cerulea ) collected in the Cumberland Mountains (Tennessee, USA; 2008&ndash;2010) as an example, we illustrate how lack of concordance between individual- and population-level measures of habitat quality can have real-world management implications.

Wildlife Society Bulletin↗

Tornadic storm avoidance behavior in breeding songbirds

Migration is a common behavior used by animals of many taxa to occupy different habitats during different periods . Migrant birds are categorized as either facultative (i.e., those that are forced to migrate by some proximal cue, often weather) or obligate (i.e., those that migrate on a regular cycle) . During migration, obligate migrants can curtail or delay flights in response to inclement weather or until favorable winds prevail , and they can temporarily reorient or reverse direction when ecological or meteorological obstacles are encountered . However, it is not known whether obligate migrants undertake facultative migrations and make large-scale movements in response to proximal cues outside of their regular migration periods . Here, we present the first documentation of obligate long-distance migrant birds undertaking a facultative migration, wherein breeding golden-winged warblers ( Vermivora chrysoptera ) carrying light-level geolocators performed a >1,500 km 5-day circumvention of a severe tornadic storm. The birds evacuated their breeding territories >24 hr before the arrival of the storm and atmospheric variation associated with it. The probable cue, radiating >1,000 km from tornadic storms , perceived by birds and influencing bird behavior and movements , is infrasound (i.e., sound below the range of human hearing). With the predicted increase in severity and frequency of similar storms as anthropogenic climate change progresses , understanding large-scale behavioral responses of animals to such events will be an important objective of future research.

Current Biology↗

Geolocators on Golden-winged Warblers do not affect migratory ecology

The use of light-level geolocators is increasingly common for connecting breeding and nonbreeding sites and identifying migration routes in birds. Until recently, the mass and size of geolocators precluded their use on songbird species weighing <12 g. Reducing the mass of geolocators, such as by shortening or eliminating the light stalk, may make their deployment on small birds feasible, but may also inhibit their ability to receive light reliably, because small geolocators can be shaded by feathers. Here we report geolocator effects on migratory ecology of Golden-winged Warblers ( Vermivora chrysoptera ) in Minnesota and Tennessee. We also evaluated whether stalk length influenced precision of location data for birds on the breeding grounds. At 8–10 g, Golden-winged Warblers are the smallest birds to be outfitted with geolocators to date. We found no differences in return rates, inter-annual territory fidelity, or body mass between geolocator-marked individuals and a control group of color-banded individuals. We observed no difference in return rates or variation in estimated breeding locations between birds marked with stalked geolocators and those with stalkless geolocators. Our results suggest that some small songbirds can be safely marked with geolocators. Light stalks appear to be unnecessary for Golden-winged Warblers; the added mass and drag of stalks can probably be eliminated on other small songbirds.

The Condor↗

Variables associated with nest survival of Golden-winged Warblers ( Vermivora chrysoptera ) among vegetation communities commonly used for nesting

A mong shrubland- and young forest-nesting bird species in North America, Golden-winged Warblers ( Vermivora chrysoptera ) are one of the most rapidly declining partly because of limited nesting habitat. Creation and management of high quality vegetation communities used for nesting are needed to reduce declines. Thus, we examined whether common characteristics could be managed across much of the Golden-winged Warbler’s breeding range to increase daily survival rate (DSR) of nests. We monitored 388 nests on 62 sites throughout Minnesota, Wisconsin, New York, North Carolina, Pennsylvania, Tennessee, and West Virginia. We evaluated competing DSR models in spatial-temporal (dominant vegetation type, population segment, state, and year), intraseasonal (nest stage and time-within-season), and vegetation model suites. The best-supported DSR models among the three model suites suggested potential associations between daily survival rate of nests and state, time-within-season, percent grass and Rubus cover within 1 m of the nest, and distance to later successional forest edge. Overall, grass cover (negative association with DSR above 50%) and Rubus cover (DSR lowest at about 30%) within 1 m of the nest and distance to later successional forest edge (negative association with DSR) may represent common management targets across our states for increasing Golden-winged Warbler DSR, particularly in the Appalachian Mountains population segment. Context-specific adjustments to management strategies, such as in wetlands or areas of overlap with Blue-winged Warblers ( Vermivora cyanoptera ), may be necessary to increase DSR for Golden-winged Warblers.

Avian Conservation and Ecology↗