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At least 613 records · Page 34Linked to original sources

Does coat colour influence survival? A test in a cyclic population of snowshoe hares

Some mammal species inhabiting high-latitude biomes have evolved a seasonal moulting pattern that improves camouflage via white coats in winter and brown coats in summer. In many high-latitude and high-altitude areas, the duration and depth of snow cover has been substantially reduced in the last five decades. This reduction in depth and duration of snow cover may create a mismatch between coat colour and colour of the background environment, and potentially reduce the survival rate of species that depend on crypsis. We used long-term (1977–2020) field data and capture–mark–recapture models to test the hypothesis that whiteness of the coat influences winter apparent survival in a cyclic population of snowshoe hares ( Lepus americanus ) at Kluane, Yukon, Canada. Whiteness of the snowshoe hare coat in autumn declined during this study, and snowshoe hares with a greater proportion of whiteness in their coats in autumn survived better during winter. However, whiteness of the coat in spring did not affect subsequent summer survival. These results are consistent with the hypothesis that the timing of coat colour change in autumn can reduce overwinter survival. Because declines in cyclic snowshoe hare populations are strongly affected by low winter survival, the timing of coat colour change may adversely affect snowshoe hare population dynamics as climate change continues.

Proceedings of the Royal Society of London Ser B.↗

Biology and conservation of the common murre in California, Oregon, Washington, and British Columbia: Vol. 1, Natural history and population trends

Over the past 30 years, the common murre ( Uria aalge californica ) has been recognized as a prominent indicator of marine conservation issues in California, Oregon, Washington, and British Columbia, especially regarding oil pollution, certain fisheries, and human disturbance. To assist the effective management of the common murre and the marine environments in which they live, this summary of available information on the biology and regional status of the common murre has been sponsored by the U.S. Fish and Wildlife Service (Division of Migratory Bird Management). In Volume 1 (Chapter 1), the natural history of the common murre is summarized, drawing heavily on breeding studies from the South Farallon Islands, California, plus a host of detailed breeding studies from the North Atlantic Ocean. Population trends of the common murre are summarized in Volume 1 (Chapter 2), focusing on changes in whole-colony counts determined from aerial photographs between the late 1970s and 1995 in California, Oregon and Washington. Historical data and human impacts to murre colonies since the early nineteenth century are also summarized. Volume 2 will summarize population threats, conservation, and management. Information presented in Volume 1 has been obtained and recorded by a large number of researchers and natural historians over two centuries. From the 1960s to 1995, most work in California, Oregon, and Washington was sponsored by the U.S. Fish and Wildlife Service, Minerals Management Service, and California Department of Fish and Game. Important breeding biology studies were conducted at the South Farallon Islands (Farallon National Wildlife Refuge) by the Point Reyes Bird Observatory, in coordination with the U.S. Fish and Wildlife Service (San Francisco Bay National Wildlife Refuge). Colony surveys in California were conducted mainly by the U.S. Fish and Wildlife Service (San Francisco Bay National Wildlife Refuge), U.S. Geological Survey (Western Ecological Research Center, Dixon Field Station), Humboldt State University, and University of California (Santa Cruz). Colony surveys in Oregon and Washington were conducted mainly by the U.S. Fish and Wildlife Service (Oregon Coast National Wildlife Refuge and Washington Maritime National Wildlife Refuges). In British Columbia, most work from the 1960s to 1995 was sponsored and conducted by the Canadian Wildlife Service and Royal British Columbia Museum.

British Columbia, California, Oregon, Washington↗

Estimating sightability of greater sage-grouse at leks using an aerial infrared system and N-mixture models

Counts of grouse present at leks (breeding grounds) during spring are widely used to monitor population numbers and assess trends. However, only a proportion of birds available to count are detected resulting in a biased population index. We designed a study using an aerial integrated infrared imaging system (AIRIS) and experimental pseudo-leks to quantify sightability (proportion of birds detected) of conventional ground-based visual (GBV) surveys for greater sage-grouse Centrocercus urophasianus . Specifically, we calibrated AIRIS at pseudo-leks composed of known numbers of captively-raised birds, primarily ring-necked pheasant Phasianus colchicus . We then carried out AIRIS and GBV surveys, simultaneously, on nearby sage-grouse leks, allowing us to model AIRIS and GBV sightability. AIRIS detected ∼93% of birds on pseudo-leks while GBV detected ∼86% of sage-grouse on leks. Thus, the ground count observation error was –14% from the ‘true' number of male sage-grouse attending the leks. We also found sagebrush cover decreased sightability for GBV counts but did not influence sightability by AIRIS. Because standard GBV protocols typically make repeated counts of sage-grouse in a single morning, we also modeled repeated GBV counts using N -mixture models and found an 88% sightability, which was nearly the same as GBV sightability from the AIRIS analysis. This suggests that the use of repeated morning counts can potentially account for imperfect detection in the standard GBV surveys currently implemented. We also provide generalized correction values that could be employed by resource managers using either GBV or AIRIS to better estimate ‘true’ numbers of sage-grouse attending leks within similar environments to this study. The findings and interpretation presented can help guide effective monitoring protocols that account for observation error and improve accuracy of data used for population trend and abundance estimation.

California, Idaho, Nevada↗

Development of a two-stage life cycle model for Oncorhynchus kisutch (coho salmon) in the upper Cowlitz River Basin, Washington

Recovery of salmon populations in the upper Cowlitz River Basin depends on trap-and-haul efforts owing to impassable dams. Therefore, successful recovery depends on the collection of out-migrating juvenile salmon at Cowlitz Falls Dam (CFD) for transport below downstream dams, as well as the collection of adults for transport upstream from the dams. Tacoma Power began downstream fish collection efforts at CFD in the mid-1990s and has been working consistently since then to improve collection efficiency to support self-sustaining salmon and steelhead ( Onchorhynchus spp.) populations in the upper Cowlitz River Basin. Although much work has focused on estimating fish collection efficiency (FCE), there has been relatively little focus on modeling population dynamics to understand how fish collection efficiency and other factors drive production of both juvenile and adult salmon over their life cycle. As a first step towards understanding the factors affecting population dynamics of Oncorhynchus kisutch (coho salmon) in the upper Cowlitz River Basin, we developed a statistical life cycle model using adult escapement and age structure data, juvenile collection data, and juvenile fish collection efficiency estimates. The goal of the statistical life cycle model is to estimate annual production and survival during two critical life-stage transitions: the freshwater production from escapement of adults upstream from CFD to collection of juveniles at CFD, and the juvenile-to-adult survival from the time of collection at the dam to the return of adults. To structure the life cycle model, we used the Ricker stock-recruitment model to estimate juvenile production from the number of parent spawners. This approach allowed us to account for density dependence at high spawner abundances while estimating annual productivity, defined as the number of juveniles produced per spawner at low spawner abundance. We then expressed productivity as a function two key variables affecting the number of juveniles collected and transported at CFD: (1) annual FCE, and (2) the annual number of days that spill occurred at CFD from September 1 to April 30. Our key findings were as follows: FCE was the primary factor affecting productivity of coho salmon upstream from CFD because FCE affects the number of juveniles that survive to continue downstream migration; Juvenile-to-adult return (JAR) rates were relatively high considering that harvest was included in the estimate, averaging about 3.6 percent and ranging as high as 9.1 percent, suggesting that adult coho salmon may be able to return to CFD at sustainable population sizes; and Much variation in the estimates of juvenile fish production upriver of CFD was unexplained even after adult escapement and FCE were accounted for, suggesting that the model may be improved by exploring different covariates and model structures for juvenile production as well as JAR rates. Additionally, by including FCE in the model, we estimated that the median pre-collection productivity, defined as the number of juveniles produced per spawner when FCE=1, was 108.4 juveniles per spawner. Because this two-stage life cycle model partitions factors that affect fish production in river compared to the ocean environment and fish life stages, the model estimates should help inform fishery managers about the overall role that fish collection at CFD may have on the recovery and sustainability of coho salmon populations.

Washington↗

Twenty-nine years of population dynamics in a small-bodied montane amphibian

Identifying population declines before they reach crisis proportions is imperative given the current global decline in vertebrate fauna and associated challenges and expense of recovery. Understanding life histories and how the environment influences demography are critical aspects of this challenge, as is determining the biological relevance of covariates that are best supported by the data. We used 29 yr of data on chorus frogs at two sites to estimate demographic parameters, examine life history, assess weather‐related covariates, and determine the magnitude of process variation in target parameters. Average estimates of survival probabilities were 0.51 (Standard Error [SE] = 0.04) and 0.43 (SE = 0.04), and average estimates of recruitment probabilities were 0.64 (SE = 0.07) and 0.44 (SE = 0.04). Process variation accounted for ≥76% of the total temporal variation in both parameters at one pond and in survival probability alone at the other, suggesting that the covariates in our top models were explaining predominantly process rather than sampling variation. Estimates of population growth rates indicated a declining population at one pond (i.e., negative population growth rates in 15 of 18 yr), and comparisons with historical estimates suggested declines in survival probability at the other. The amount of deviance explained was low, providing little support for the influence of covariates on target parameters, despite model selection support. Synthesis and applications: This analysis illustrates the value of disentangling components of variance when assessing demographic drivers and highlights the need for adequate demographic information in assigning conservation labels.

Ecosphere↗

Distribution, population status and trends of Kittlitz's murrelet Brachyramphus brevirostris in Lower Cook Inlet and Kachemak Bay, Alaska

Lower Cook Inlet (LCI) in south-central Alaska is unusual among the breeding areas of Kittlitz's Murrelet Brachyramphus brevirostris because of human impacts on the marine and terrestrial environments and because of the lack of tidewater glaciers. In LCI the Kittlitz's Murrelet co-exists with the more abundant Marbled Murrelet, which complicates abundance estimates because of the difficulty of species identification. We compared survey data for an area with overlapping coverage in LCI (Core area) in 1993 (June) and from 1996 to 1999 (July-early August). Within this LCI Core area, the surveys in 1996-1999 estimated ~1600 Kittlitz's Murrelets and ~17 000 Marbled Murrelets, including prorated unidentified murrelets. The Kittlitz's Murrelet population declined between 1993 and 1999 at 26% per annum (84% overall). Simultaneously, Marbled Murrelets declined by 12% per annum (56% overall), though the decline was not statistically significant. Declines were estimated conservatively because the 1993 survey was conducted in June, when both murrelet species are less abundant on the water. We also surveyed Kachemak Bay, a large embayment of LCI, during mid-summer (July) of 2005-2007 and estimated a population of 2047 Kittlitz's Murrelets (SD 1120, n = 3 years) residing primarily in the inner bay. Marbled Murrelets numbered 11 040 (SD 1306) and were found throughout the bay. On one transect set in inner Kachemak Bay, Kittlitz's Murrelet density in late summer (1-16 August) declined 7.5% per annum between 1988 and 2007 (n = 6 years), and Marbled Murrelet density increased 4.9% per annum. On two other transect sets in the inner bay, however, neither murrelet species showed a change in density between 1996 and 2007. Inner Kachemak Bay is a persistent hotspot for Kittlitz's Murrelet and may attract murrelets from LCI and beyond. We recommend monitoring murrelet populations in Kachemak Bay, although Kittlitz's Murrelets likely move between the main body of Cook Inlet and Kachemak Bay, and a complete LCI survey is needed to gauge regional population trends.

Marine Ornithology: Journal of Seabird Research an↗

Conspecific and congeneric interactions shape increasing rates of breeding dispersal of northern spotted owls

Breeding dispersal, the movement from one breeding territory to another, is rare for philopatric species that evolved within relatively stable environments, such as the old-growth coniferous forests of the Pacific Northwest. Although dispersal is not inherently maladaptive, the consequences of increased dispersal on population dynamics in populations whose historical dispersal rates are low could be significant, particularly for a declining species. We examined rates and possible causes of breeding dispersal based on a sample of 4,118 northern spotted owls ( Strix occidentalis caurina ) monitored in seven study areas over 28 yr, 1990–2017, in Oregon and Washington, USA. Using a multistate mark–resight analysis, we investigated the potential impacts of an emergent congeneric competitor (barred owl Strix varia ) and forest alteration (extrinsic factors), and social and individual conditions (intrinsic factors) on 408 successive and 1,372 nonsuccessive dispersal events between years. The annual probability of breeding dispersal increased for individual owls that had also dispersed in the previous year and decreased for owls on territories with historically high levels of reproduction. Intrinsic factors including pair status, prior reproductive success, and experience at a site, were also associated with breeding dispersal movements. The percent of monitored owls dispersing each year increased from ˜7% early in the study to ˜25% at the end of the study, which coincided with a rapid increase in numbers of invasive and competitively dominant barred owls. We suggest that the results presented here can inform spotted owl conservation efforts as we identify factors contributing to changing rates of demographic parameters including site fidelity and breeding dispersal. Our study further shows that increasing rates of breeding dispersal associated with population declines contribute to population instability and vulnerability of northern spotted owls to extinction, and the prognosis is unlikely to change unless active management interventions are undertaken.

California, Oregon, Washington↗

Intraspecific variation in masting across climate gradients is inconsistent with the environmental stress hypothesis

Year-to-year variation in seed crop size (i.e., masting) varies strongly among populations of the same species. Understanding what causes this variation is vital, as masting affects the ability of tree species to regenerate and determines the population dynamics of a wide variety of animals. It is commonly thought that environmental stress is a key driver of masting variability. The environmental stress hypothesis posits that more marginal conditions increase the strength of masting. Using 437 time series from 19 tree species, we find that this hypothesis fails to fully explain how masting varies across marginality gradients. We expected higher interannual variation and less frequent masting events at species margins but instead found that while mast years are indeed less frequent, the interannual variation was lower toward the margins. The observed patterns suggest that populations growing at the margins may invest more resources in low seed production years compared with their conspecifics, hedging their bets in these more challenging environments.

Ecology↗

Fire-related plant traits

As illustrated in Fig. 2.1 there are four environmental parameters that are necessary to determine the distribution of fire-prone ecosystems. However, they are insufficient to predict ecosystem responses to fire without a detailed understanding of the fire regime (see Fig. 2.7). Different fire regimes have very different potentials for recovery and place very different premiums on specific plant traits. For example, those traits contributing to the persistence of species in crown fire regimes will often be very different from those in surface fire regimes. In short, organisms are not adapted to fire per se , but rather to a particular fire regime. Plant traits that are adaptive in fire-prone environments are discussed here. The evolution of such traits and the extent to which they represent adaptations to fire are considered in Chapter 9. Plant populations exhibit four modes of recovery following fire: endogenous regeneration from resprouts or fire-triggered seedling recruitment, delayed seedling recruitment from postfire resprout seed production, delayed seedling recruitment from in situ surviving parent plants, or colonization from unburned metapopulations.

Book chapter↗

Hydrologic characteristics of freshwater mussel habitat: novel insights from modeled flows

The ability to model freshwater stream habitat and species distributions is limited by the spatially sparse flow data available from long-term gauging stations. Flow data beyond the immediate vicinity of gauging stations would enhance our ability to explore and characterize hydrologic habitat suitability. The southeastern USA supports high aquatic biodiversity, but threats, such as landuse alteration, climate change, conflicting water-resource demands, and pollution, have led to the imperilment and legal protection of many species. The ability to distinguish suitable from unsuitable habitat conditions, including hydrologic suitability, is a key criterion for successful conservation and restoration of aquatic species. We used the example of the critically endangered Tar River Spinymussel ( Parvaspina steinstansana ) and associated species to demonstrate the value of modeled flow data (WaterFALL™) to generate novel insights into population structure and testable hypotheses regarding hydrologic suitability. With ordination models, we: 1) identified all catchments with potentially suitable hydrology, 2) identified 2 distinct hydrologic environments occupied by the Tar River Spinymussel, and 3) estimated greater hydrological habitat niche breadth of assumed surrogate species associates at the catchment scale. Our findings provide the first demonstrated application of complete, continuous, regional modeled hydrologic data to freshwater mussel distribution and management. This research highlights the utility of modeling and data-mining methods to facilitate further exploration and application of such modeled environmental conditions to inform aquatic species management. We conclude that such an approach can support landscape-scale management decisions that require spatial information at fine resolution (e.g., enhanced National Hydrology Dataset catchments) and broad extent (e.g., multiple river basins).

North Carolina↗

Ecological and social drivers of Mexican wolf home range size across spatiotemporal scales

Elucidating factors influencing home range size is fundamental to the ecology and management of wildlife species, particularly those of conservation concern, because they can provide insight into how species utilize and interact with their environment. Variation in home range size can be related to intraspecific competition and social organization, energetic requirements in relation to habitat productivity, allometric relationships, and population density. The Mexican Gray Wolf ( Canis lupus baileyi ) is an endangered subspecies of the Gray Wolf whose home range size has not yet been studied. We examined ecological and social drivers of home range size of 22 Mexican Wolf packs between 2017 and 2021 across 4 biological time frames: annual; denning; post-denning; and non-denning. We used a 95% Brownian Bridge Movement Model home range estimator and generalized linear mixed-effect models to assess these relationships. Home range size was inversely correlated with estimated ungulate biomass, which was the most influential driver of home range size at annual and post-denning time frames. Larger packs utilized larger ranges during denning and post-denning time frames, while packs with larger litters had smaller ranges during the denning season. Snow depth was inversely related to home range size during the non-denning season. Our results indicate that both ecological and social factors are important and seasonally dependent in driving Mexican Wolf home range size. Use of a multiscale approach in future home range studies could discern relevant factors for species during time frames of interest.

Journal of Mammology↗

Spatial distribution of larval Ixodes scapularis (Acari:Ixodidae) on Peromyscus leucopus and Microtus pennsylvanicus at two island sites

Larval blacklegged ticks, Ixodes scapularis , were collected from white-footed mice, Peromyscus leucopus , on Prudence Island (where Microtus pennsylavanicus were not captured) and from meadow voles, M. pennsylvanicus , on Patience Island (where P. leucopus was absent) in Narragansett Bay, Rhode Island from June to October 1992. Ixodes scapularis larvae were also collected by flagging in the vicinity of host captures. On both islands, the relative density of larvae changed from July to September in samples from hosts, but not in flagging samples. Consequently, different sampling techniques can give different assessments of tick populations. Larvae were highly aggregated on both of the host species throughout the sampling period. As the mean relative density of larvae increased in the environment (based on flagging samples), larvae on the hosts became more dense and more crowded. Increased densities of larvae in the environment were not correlated with increased patchiness in the distribution of larvae among host animals on either island. Changes in the spatial distribution of larval I. scapularis on each host species had similar trends as larval densities and distributions within the environment. These results suggest that M. pennsylvanicus can serve as an alternative host for immature I. scapularis in a P. leucopus -free environment and have similar distributional characteristics.

Journal of Parasitology↗

U.S. Geological Survey response to white-nose syndrome in bats

Overview Since its discovery in 2007, the fungal disease known as white-nose syndrome (WNS) has killed more than six million bats. Ten of 47 bat species have been affected by WNS across 32 States and 5 Canadian Provinces. The cold-growing fungus ( Pseudogymnoascus destructans ) that causes WNS infects skin covering the muzzle, ears, and wings of hibernating bats. The fungus erodes deep into the vitally important skin of bat wings and fatally disrupts hibernation of bats through physical damage and energy depletion as they try to cope with infection. U.S. Geological Survey (USGS) science has been critical in identifying the causal fungus, characterizing the effects of WNS, and tracking the fungus as it rapidly spreads through many populations of bats in North America. Early USGS research enhanced our understanding of how WNS affects individual bats and how the fungus persists in the environment. Today, USGS scientists are engaged in a nationwide response to WNS, in close coordination with our partners at the U.S. Fish and Wildlife Service (USFWS), National Park Service (NPS), and U.S. Forest Service (USFS).

Fact Sheet↗

Characterizing urban heat islands across 50 major cities in the United States

Urban development and associated land-cover and land-use change alters the environment. The continued increase of developed land changes the Earth’s ecosystems and affects the resources provided to society. During the last 40 years, urban population in the United States has increased by more than 6.3 percent, and more than 80 percent of the U.S. population resides in urban areas. One of the changes associated with urbanization is the change of landscape features to structures such as buildings, roads, and other infrastructure that absorb and re-emit the heat of the sun more than natural landscapes such as forests and water bodies. This land-cover transition can result in an urban surface temperature that is higher than in a non-urban area, which is defined as a surface urban heat island (SUHI). A SUHI has a profound effect on the lives of urban residents and can exacerbate the risk of heat-related mortality associated with global climate change. The change of urban landscapes and climate conditions can affect the SUHI intensity. The U.S. Geological Survey (USGS) has developed a dataset of SUHI intensity and change from 1985 to 2020 over 50 cities in the United States using Landsat surface temperature (ST) and land - cover data. The data reveal SUHI spatial distributions and temporal trends in these cities. The 50-city mean SUHI intensity reaches 2.88 degrees Celsius (°C) (5.19 degrees Fahrenheit [°F]) and an average trend of 0.32 °C per decade (0.58 °F per decade). The data also provide spatial distributions of hotspots where annual mean ST is higher than in the surrounding areas that have the same urban land-cover type and high ST that repeated more than 50 percent of the time during 1985–2020 for 50 cities.

Fact Sheet↗

Coastal effects

The Coasts chapter of the Third National Climate Assessment, published in 2014, focused on coastal lifelines at risk, economic disruption, uneven social vulnerability, and vulnerable ecosystems. This Coastal Effects chapter of the Fourth National Climate Assessment updates those themes, with a focus on integrating the socioeconomic and environmental impacts and consequences of a changing climate. Specifically, the chapter builds on the threat of rising sea levels exacerbating tidal and storm surge flooding, the state of coastal ecosystems, and the treatment of social vulnerability by introducing the implications for social equity. U.S. coasts are dynamic environments and economically vibrant places to live and work. As of 2013, coastal shoreline counties were home to 133.2 million people, or 42% of the population. The coasts are economic engines that support jobs in defense, fishing, transportation, and tourism industries; contribute substantially to the U.S. gross domestic product; and serve as hubs of commerce, with seaports connecting the country with global trading partners. Coasts are home to diverse ecosystems such as beaches, intertidal zones, reefs, seagrasses, salt marshes, estuaries, and deltas that support a range of important services including fisheries, recreation, and coastal storm protection. U.S. coasts span three oceans, as well as the Gulf of Mexico, the Great Lakes, and Pacific and Caribbean islands. The social, economic, and environmental systems along the coasts are being affected by climate change. Threats from sea level rise (SLR) are exacerbated by dynamic processes such as high tide and storm surge flooding (Ch. 19: Southeast, KM 2) , erosion (Ch. 26: Alaska, KM 2) , waves and their effects, saltwater intrusion into coastal aquifers and elevated groundwater tables (Ch. 27: Hawaiʻi & Pacific Islands, KM 1; Ch. 3: Water, KM 1) , local rainfall (Ch. 3: Water, KM 1) , river runoff (Ch. 3: Water, KM 1) , increasing water and surface air temperatures (Ch. 9: Oceans, KM 3) , and ocean acidification (see Ch. 2: Climate, KM 3 and Ch. 9: Oceans, KM 1, 2, and 3 for more information on ocean acidification, hypoxia, and ocean warming) . Although storms, floods, and erosion have always been hazards, in combination with rising sea levels they now threaten approximately $1 trillion in national wealth held in coastal real estate and the continued viability of coastal communities that depend on coastal water, land, and other resources for economic health and cultural integrity (Ch. 15: Tribes, KM 1 and 2) .

Report↗

Wolves and caribou in Denali National Park, Alaska

Management of gray wolves ( Canis lupus ) and their prey in interior Alaska has been controversial for three decades (Harbo and Dean 1983). Recently, debate was rekindled with renewed interest in wolf control to bolster two populations of caribou ( Rangifer tarandus ). Our research in Denali National Park provides insights into the declines in caribou numbers over the last few years that are the basis of recent wolf control proposals. Our observations of fluctuating populations also illustrate the complexity of managing these predator-prey systems to meet a diverse array of public interests. Wolves and caribou are two components of the large mammal community of Denali National Park that also includes grizzly bears ( Ursus arctos ), moose ( Alces alces ), and Dall sheep ( Ovis dalli ). With the 1980 park expansion to more than 18,800 km2 (7,300 mi2) of central Alaska, this large mammal system became the only one of its kind that is virtually unaffected by human harvest. Therefore, Denali provides a unique opportunity to understand the natural interactions of these species and serves as a baseline for comparison with areas where hunting or other active wildlife management occurs. We have studied Denali's wolves and caribou since 1986 to determine their numbers and status and understand their natural interactions in this protected subarctic ecosystem. Our studies began near the end of more than a decade of mostly light winter snowfalls of around 100 cm (39 in)/yr. Since winter 1988-89, we have experienced five consecutive winters with above-average snowfalls, including two record-setting years. During winters 1990-91 and 1992-93, more than 390 cm (154 in) of snow fell, four times as much as in the early years of our study. This change in snowfall had profound effects on the wildlife in central Alaska. The population trends of Denali's caribou and wolves are strong evidence of the natural fluctuations to be expected in species inhabiting such dynamic and variable environments.

Alaska↗

Long-term persistence of horse fecal DNA in the environment makes equids particularly good candidates for non-invasive sampling

Fecal DNA collected noninvasively can provide valuable information about genetic and ecological characteristics. This approach has rarely been used for equids, despite the need for conservation of endangered species and management of abundant feral populations. We examined factors affecting the efficacy of using equid fecal samples for conservation genetics. First, we evaluated two fecal collection methods (paper bag vs. ethanol). Then, we investigated how time since deposition and month of collection impacted microsatellite amplification success and genotyping errors. Between May and November 2014, we collected feral horse fecal samples of known age each month in a feral horse Herd Management Area in western Colorado and documented deterioration in the field with photographs. Samples collected and dried in paper bags had significantly higher amplification rates than those collected and stored in ethanol. There was little difference in the number of loci that amplified per sample between fresh fecal piles and those that had been exposed to the environment for up to 2 months (in samples collected in paper bags). After 2 months of exposure, amplification success declined. When comparing fresh (0–2 months) and old (3–6 months) fecal piles, samples from fresh piles had more matching genotypes across samples, better amplification success and less allelic dropout. Samples defecated during the summer and collected within 2 months of deposition had highest number of genotypes matching among samples, and lowest rates of amplification failure and allelic dropout. Due to the digestive system and amount of fecal material produced by equids, as well as their occurrence in arid ecosystems, we suggest that they are particularly good candidates for noninvasive sampling using fecal DNA.

Colorado↗

Monitoring planktivorous seabird populations: Validating surface counts of crevice-nesting auklets using mark-resight techniques

Least Auklets ( Aethia pusilla (Pallas, 1811)) are the most abundant species of seabird in the Bering Sea and offer a relatively efficient means of monitoring secondary productivity in the marine environment. Counting auklets on surface plots is the primary method used to track changes in numbers of these crevice-nesters, but counts can be highly variable and may not be representative of the number of nesting individuals. We compared average maximum counts of Least Auklets on surface plots with density estimates based on mark–resight data at a colony on St. Lawrence Island, Alaska, during 2001–2004. Estimates of breeding auklet abundance from mark–resight averaged 8 times greater than those from maximum surface counts. Our results also indicate that average maximum surface counts are poor indicators of breeding auklet abundance and do not vary consistently with auklet nesting density across the breeding colony. Estimates of Least Auklet abundance from mark–resight were sufficiently precise to meet management goals for tracking changes in seabird populations. We recommend establishing multiple permanent banding plots for mark–resight studies on colonies selected for intensive long-term monitoring. Mark–resight is more likely to detect biologically significant changes in size of auklet breeding colonies than traditional surface count techniques.

Canadian Journal of Zoology↗