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118 records · Page 7Linked to original sources
USGS2010

Distribution and conservation standing of West Virginia crayfishes

The diversity of crayfishes in West Virginia represents a transition between the species-rich southern Appalachian faunas and the depauperate crayfish diversity in the northeastern United States. Currently, 22 described species occur in the state, of which 6 are given S1 status, and 3 are introduced species. One species, Orconectes limosus (Spinycheek Crayfish) is considered extirpated within the past decade. Imperiled species include Cambarus veteranus (Big Sandy Crayfish), Cambarus elkensis (Elk River Crayfish), Cambarus longulus (Atlantic Slope Crayfish), and Cambarus nerterius (Greenbrier Cave Crayfish). Three species— O. virilis (Virile Crayfish), Orconectes rusticus (Rusty Crayfish), and Procambarus zonangulus (Southern White River Crawfish)—have introduced populations within the state. Procambarus acutus (White River Crawfish) occurs in bottomland forest along the Ohio River floodplain, and is considered native. Several undescribed taxa have been identified and currently are being described. A statewide survey was initiated in 2007 to document the current distribution and conservation status of crayfishes in West Virginia.

West Virginia↗
USGS2003

Effects of desert wildfires on desert tortoise (Gopherus agassizii) and other small vertebrates

We report the results of standardized surveys to determine the effects of wildfires on desert tortoises (Gopherus agassizii) and their habitats in the northeastern Mojave Desert and northeastern Sonoran Desert. Portions of 6 burned areas (118 to 1,750 ha) were examined for signs of mortality of vertebrates. Direct effects of fire in desert habitats included animal mortality and loss of vegetation cover. A range of 0 to 7 tortoises was encountered during surveys, and live tortoises were found on all transects. In addition to desert tortoises, only small (<1 kg) mammals and reptiles (11 taxa) were found dead on the study areas. We hypothesize that indirect effects of fire on desert habitats might result in changes in the composition of diets and loss of vegetation cover, resulting in an increase in predation and loss of protection from temperature extremes. These changes in habitat also might cause changes in vertebrate communities in burned areas.

Southwestern Naturalist↗
USGS2020

Sixty years of White-tailed Deer (Odocoileus virginianus) yarding in a Gray Wolf (Canis lupus)–deer system

This article synthesizes information from over a six-decade period of studies of White-tailed Deer ( Odocoileus virginianus ) use of a winter yard and subject to Gray Wolf ( Canis lupus ) predation in northeastern Minnesota. It also adds spring migration data from 35 adult female deer and fawns studied there during 1998, 1999, 2001, 2014, and 2017. Twenty-nine of these deer migrated in spring a mean distance of 29 km (SE = 4), a maximum distance of 78 km, and at a mean bearing of 83° (SE = 12; range 21–348). These findings are similar to those from 49 deer (both sexes) from the same yard studied during 1974–1984, that migrated a mean distance of 25 km (SE = 1.8) and a mean bearing of 77° ± 4 SE. Between the two periods, the wolf population fluctuated considerably, the winter range of deer in the area where these deer spent summer greatly diminished, and both derechos and fires disturbed the habitat. This study attests to the selective advantage of the migratory tradition of deer in this yard.

Minnesota↗
USGS2018

Weekly summer diet of gray wolves (Canis lupus) in northeastern Minnesota

Wolves ( Canis lupus ) are opportunistic predators and will capitalize on available abundant food sources. However, wolf diet has primarily been examined at monthly, seasonal, or annual scales, which can obscure short-term responses to available food. We examined weekly wolf diet from late June to early October by collecting scats from a single wolf pack in northeastern Minnesota. During our 15 week study, nonungulate food types constituted 58% of diet biomass. Deer ( Odocoileus virginianus ) fawns were a major food item until mid-July after which berries (primarily Vaccinium and Rubus spp.) composed 56–83% of weekly diet biomass until mid-August. After mid-August, snowshoe hares ( Lepus americanus ) and adult deer were the primary prey. Weekly diet diversity approximately doubled from June to October as wolves began using several food types in similar proportions as the summer transitioned into fall. Recreational hunting of black bears ( Ursus americanus ) contributed to weekly wolf diet in the fall as wolves consumed foods from bear bait piles and from gut piles/carcasses of successfully harvested or fatally wounded bears. To our knowledge, we are the first to examine wolf diet via scat analysis at weekly intervals, which enabled us to provide a detailed description of diet plasticity of this wolf pack, as well as the rapidity with which wolves can respond to new available food sources.

Minnesota↗
USGS2015

Experimental evidence of spatial memory and home range affinity in White-tailed Deer ( Odocoileus virginianus )

The role of spatial memory in the movement of animals through landscapes remains elusive. To examine spatial memory and home range affinity of White-tailed Deer ( Odocoileus virginianus ) in northeastern Minnesota during 1995–2007, I translocated 17 adult does with known home ranges to unfamiliar sites and radio-tracked them after their release. Twelve does wearing transmitting radio-collars returned to their home ranges. Death and collar expiration precluded determination of whether the remaining five does would have returned to home ranges. Three of five does wearing global positioning system collars traveled throughout hundreds of square kilometres, circling, backtracking, and returning to release sites, while two others exhibited directional movement for tens of kilometres. Four does that survived to parturition stopped traveling and moved at hourly rates similar to those of control does during the first three weeks of the typical fawn-rearing period, but continued traveling later. Their aberrant extensive travel before and after interruption by parturition suggests that they recognized they were in unfamiliar areas, demonstrating both their capacity and propensity to search for and occupy the familiar space of their individual home ranges. Their successful return to home ranges provided experimental evidence of spatial memory and further elucidated its pervasive role in White-tailed Deer spatial ecology.

Canadian Field-Naturalist↗
USGS2013

Abundance, distribution, and population trends of the iconic Hawaiian Honeycreeper, the ʻIʻiwi (Vestiaria coccinea) throughout the Hawaiian Islands

Naturalists in the 1800s described the ʻIʻiwi (Vestiaria coccinea) as one of the most abundant forest birds, detected in forested areas from sea level to tree line across all the major Hawaiian Islands. However, in the late 1800s, ʻIʻiwi began to disappear from low elevation forests, and by the mid-1900s, the species was largely absent from low- and mid-elevation areas. Today, ʻIʻiwi are restricted to high-elevation forests on the islands of Hawaiʻi, east Maui, and Kauaʻi, with a few birds apparently persisting on Oʻahu, Molokaʻi, and west Maui. ʻIʻiwi are highly vulnerable to introduced disease, and the prevalence of avian malaria in low and mid-elevations is believed to be the cause of ʻIʻiwi being restricted to high elevations where temperatures are too cold for the development of the disease and its mosquito vector. With global warming, it is feared that the disease will move quickly into the high-elevation forests where the last ʻIʻiwi reside, threatening their viability. The U.S. Fish and Wildlife Service was petitioned to list the ʻIʻiwi as an Endangered Species in 2010, and this report provides a comprehensive review of the abundance, distribution, and trends using historical survey data as well as the most recently available survey information (up to 2012). We estimate the total population size of ‘I‘iwi at 550,972–659,864 (mean = 605,418) individuals. Of these, 90 percent are on the island of Hawaiʻi, followed by east Maui (about 10 percent), with less than 1 percent on Kauaʻi. ʻIʻiwi population trends vary across the islands. ʻIʻiwi population in Kauaʻi has experienced sharp declines, with a projected trend of 92 percent decline over a 25 year period based on the 2000–2012 surveys. On East Maui, the northeastern region has experienced declines (34 percent over a 25 year period), while the southeastern region has been stable to moderately increasing. On the island of Hawaiʻi, population trends are mixed. On the windward side, populations are largely declining, although the northern section (Hakalau Forest) has stable populations. On the leeward side, results suggest a strongly increasing population, with estimates of as much as a 147 percent increase over a 25 year period from the Puʻu Waʻawaʻa region. However, it is unclear how much these results from the leeward side of Hawaiʻi show a population trend contrary to population trends in all other areas or are an artifact of a sparsely sampled area. Trends by elevation suggest a large decrease in numbers of ʻIʻiwi at elevations below 1,200 meters on Kauaʻi and northeast Maui. Low elevation ʻIʻiwi populations also appear to have decreased in other regions, although low-elevation areas are not surveyed as often as other areas because of their lack of native forest birds. An exception to this pattern was the lower portions of the Hakalau Forest National Wildlife Refuge Kona Unit in the central leeward part of the island of Hawaiʻi, where populations appeared stable at the lower elevations. Based on the most recent surveys (up to 2012), approximately 50 percent of ʻIʻiwi live in a narrow, 500-meter band at elevations of 1,200–1,700 meters, suggesting that ʻIʻiwi are vulnerable to future shifts in climate.

Hawai'i↗
USGS2016

Diet of pumas ( Puma concolor ) in Sonora, Mexico, as determined by GPS kill sites and molecular identified scat, with comments on jaguar ( Panthera onca ) diet

We documented puma ( Puma concolor ) and jaguar ( Panthera onca ) prey consumption in northeastern Sonora, Mexico, by investigating global positioning system cluster sites ( n = 220), and conducting molecular analyses of scat ( n = 116) collected between 2011 and 2013. We used camera trap data ( n = 8,976 camera days) to estimate relative abundances of pumas and jaguars. Deer ( Odocoileus virginianus ) was the most frequent prey for puma found at kill sites (67%) and identified from scat (74%), although based on relative numbers of prey consumed, deer represented 45% and lagomorphs 20% of the proportion of all individuals eaten. A variety of small prey (weighing <15 kg) comprised the majority (52%) of the jaguar kill sites. From prey found at kill sites, jaguars killed calves ( Bos taurus ) at a lower frequency than previously reported, whereas pumas preyed on calves at a higher frequency than previously reported in the same area. In our study area, jaguars preyed on calves at approximately the same rate as pumas (jaguars 3.7 calves per year, pumas 4.9 calves per year). Calculated predation rates were limited only to collared animals within our study area and therefore should not be considered applicable to all pumas and jaguars in Sonora.

Sonora↗
USGS2017

White-tailed deer (Odocoileus virginianus) subsidize gray wolves (Canis lupus) during a moose (Alces americanus) decline: A case of apparent competition?

Moose ( Alces americanus ) in northeastern Minnesota have declined by 55% since 2006. Although the cause is unresolved, some studies have suggested that Gray Wolves ( Canis lupus ) contributed to the decline. After the Moose decline, wolves could either decline or switch prey. To determine which occurred in our study area, we compared winter wolf counts and summer diet before and after the Moose decline. While wolf numbers in our study area nearly doubled from 23 in winter 2002 to an average of 41 during winters 2011–2013, calf:cow ratios (the number of calves per cow observed during winter surveys) in the wider Moose range more than halved from 0.93 in 2002 to an average of 0.31 during 2011–2013. Compared to summer 2002, wolves in summers 2011–2013 consumed fewer Moose and more White-tailed Deer ( Odocoileus virginianus ). While deer densities were similar during each period, average vulnerability, as reflected by winter severity, was greater during 2011–2013 than 2002, probably explaining the wolf increase. During the wolf increase Moose calves remained a summer food item. These findings suggest that in part of the Moose range, deer subsidized wolf numbers while wolves also preyed on Moose calves. This contributed to a Moose decline and is a possible case of apparent competition and inverse-density-dependent predation.

Canadian Field-Naturalist↗
USGS2012

Spatio-temporal variations in age structures of a partially re-established population of northern river otters ( Lontra canadensis )

Examination of age structures and sex ratios is useful in the management of northern river otters ( Lontra canadensis ) and other furbearers. Reintroductions and subsequent recolonizations of river otters have been well documented, but changes in demographics between expanding and established populations have not been observed. As a result of reintroduction efforts, immigration from Arkansas and northeastern Texas, and other efforts, river otters have become partially reestablished throughout eastern and central Oklahoma. Our objective was to examine age structures of river otters in Oklahoma and identify trends that relate to space (watersheds, county) and time (USDA Animal and Plant Health Inspection Service county trapping records). We predicted that river otters in western areas of the state were younger than river otters occurring farther east. From 2005&ndash;2007, we obtained salvaged river otter carcasses from federal and state agencies, and we live-captured other river otters using leg hold traps. Seventy-two river otters were sampled. Overall, sex ratios were skewed toward females (1F∶0.8M), but they did not differ among spatiotemporal scales examined. Teeth were removed from salvaged and live-captured river otters (n = 63) for aging. One-year old river otters represented the largest age class (30.2%). Proportion of juveniles (<1 y old) in Oklahoma (19.0%) was less than other states. Mean age of river otters decreased from east-to-west in the Arkansas River and its tributaries. Mean age of river otters differed between the Canadian River Watershed (0.8 y) and the Arkansas River Watershed (2.9 y) and the Canadian River Watershed and the Red River Watershed (2.4 y). Proportion of juveniles did not differ among spatiotemporal scales examined. Similar to age structure variations in other mammalian carnivores, colonizing or growing western populations of river otters in Oklahoma contained younger ages than more established eastern populations.

American Midland Naturalist↗
USGS2007

Waterfowl distribution and abundance during spring migration in Southern Oregon and Northeastern California

We used aerial surveys to study abundance and distribution of waterfowl (ducks, geese, swans, and coots) during spring in southern Oregon and northeastern California (SONEC). Total waterfowl-use days in SONEC during the 119-day, 5 January-3 May, spring period was similar during 2002 (127,977,700) and 2003 (128,076,200) and averaged 1,075,900 birds per day (bpd); these estimates should be adjusted upward 4%-10% to account for areas not surveyed. Waterfowl abundance peaked in mid-March in both years: 2,095,700 in 2002 and 1,681,700 in 2003. Northern Pintail (Anas acuta) was the most abundant species in both years, accounting for 25.6% of the 2002 and 24.5% of the 2003 waterfowl-use days. Pintail abundance peaked during the 13 March survey at 689,300 in 2002 and 532,100 in 2003. All other dabbling ducks accounted for 27.6% and 28.6%, diving ducks for 13.5% and 9.2%, geese for 24.6% and 29.3%, swans for 2.8% and 1.0%, and coots for 5.8% and 6.4% of the spring waterfowl-use days in SONEC during 2002 and 2003, respectively. Although use days changed little for total waterfowl (+0.08%) and dabbling ducks (-0.1%), diving duck use was lower (-32%), and goose use days were greater (+19%) in 2003 than in 2002. Distribution was similar in both years, with the most waterfowl use in the Lower (66%) and Upper (14%) Klamath subregions; 2%-6% occurred in each of the other subregions. Although the Lower Klamath subregion received the greatest overall waterfowl use, distribution among subregions varied among species and surveys, and all subregions were important during some part of the spring for 1 or more species. Peak spring abundance in SONEC during 2002 and 2003 averaged 50.3% of the midwinter abundance in California (all survey regions) and southern Oregon (69-3 survey region) for all waterfowl, 46.1% for dabbling ducks, 62.4% for diving ducks, 68.8% for geese, 109.4% for swans, and 43.8% for coots. Each spring, 75% of all waterfowl use in SONEC occurred on federal, state, or Nature Conservancy lands (i.e., protected areas). On protected areas there was a higher percentage of dabbling ducks (80.5%), geese (70.5%), and coots (81.5%) than diving ducks (60.4%) and swans (49%). Waterfowl use of Klamath Basin National Wildlife Refuge (NWR) averaged 42% greater during spring 2002-2003 (568,500 bpd) than during 1998-2001 (Gilmer et al. 2004). Numerous factors likely impacted magnitude and distribution of waterfowl use of SONEC during spring, including weather, waterfowl populations, SONEC habitat, and species ecology. SONEC is a critical spring staging area for waterfowl that winter in the Central Valley of California and other Pacific Flyway regions and should be a major focus area for waterfowl-habitat conservation efforts.

Western North American Naturalist↗