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At least 253 records · Page 14Linked to original sources

Optimal use of resources structures home ranges and spatial distribution of black bears

Research has shown that territories of animals are economical. Home ranges should be similarly efficient with respect to spatially distributed resources and this should structure their distribution on a landscape, although neither has been demonstrated empirically. To test these hypotheses, we used home range models that optimize resource use according to resource-maximizing and area-minimizing strategies to evaluate the home ranges of female black bears, Ursus americanus, living in the southern Appalachian Mountains. We tested general predictions of our models using 104 home ranges of adult female bears studied in the Pisgah Bear Sanctuary, North Carolina, U.S.A., from 1981 to 2001. We also used our models to estimate home ranges for each real home range under a variety of strategies and constraints and compared similarity of simulated to real home ranges. We found that home ranges of female bears were efficient with respect to the spatial distribution of resources and were best explained by an area-minimizing strategy with moderate resource thresholds and low levels of resource depression. Although resource depression probably influenced the spatial distribution of home ranges on the landscape, levels of resource depression were too low to quantify accurately. Home ranges of lactating females had higher resource thresholds and were more susceptible to resource depression than those of breeding females. We conclude that home ranges of animals, like territories, are economical with respect to resources, and that resource depression may be the mechanism behind ideal free or ideal preemptive distributions on complex, heterogeneous landscapes. ?? 2007 The Association for the Study of Animal Behaviour.

Animal Behaviour

Acceptability of residential development in a regional landscape: Potential effects on wildlife occupancy patterns

The conversion of natural lands to developed uses may pose the single greatest human threat to global terrestrial biodiversity. Continued human growth and development over the next century will further exacerbate these effects of habitat loss and fragmentation. Natural resource managers are tasked with managing wildlife as a public trust, yet often have little say in land use decisions. Generally speaking, decision makers could benefit from an understanding of what different regulations mean in terms of wildlife distribution. In a previous paper ( Bettigole et al., 2013 ), we surveyed town residents throughout Vermont to measure how respondents feel about a range of development levels within their town boundaries. We estimated the “social carrying capacity for development” – or SK d – for 251 towns in Vermont. SK d provides an estimate of the level of developed land cover classes that town residents deem “acceptable” within their town boundaries. In this paper, we design a framework for linking the town-specific SK d estimates with the wildlife distribution patterns for three wide-ranging mammalian species: American black bear ( Ursus americanus ), fisher ( Martes pennanti ), and bobcat ( Lynx rufus ). We simulated landscape conditions at SK d for each town in Vermont, and then used existing occupancy models for the three target species to spatially map and compare occupancy rates in the baseline year 2000 with occupancy rates at SK d . With nearly 90% of Vermont towns willing to increase developed landcover classes within town boundaries compared to baseline levels, significant state-wide changes in occupancy rates were predicted for all three focal species. Average occupancy rates declined by −15.9% and −3.1% for black bear and bobcats, respectively. Average occupancy rates for fisher increased by 9.0%. This study provides a method for linking development standards within a town with wildlife occurrence. Across towns, the methodology spatially identifies areas that may be at risk of future development, as well as identifying areas where wildlife distribution patterns may face future change as a result of increased human population growth and development.

Biological Conservation

Relative influences of climate change and human activity on the onshore distribution of polar bears

Climate change is altering habitat for many species, leading to shifts in distributions that can increase levels of human-wildlife conflict. To develop effective strategies for minimizing human-wildlife conflict, we must understand the relative influences that climate change and other factors have on wildlife distributions. Polar bears (Ursus maritimus) are increasingly using land during summer and autumn due to sea ice loss, leading to higher incidents of conflict and concerns for human safety. We sought to understand the relative influence of sea ice conditions, onshore habitat characteristics, and human-provisioned food attractants on the distribution and abundance of polar bears while on shore. We also wanted to determine how mitigation measures might reduce human-polar bear conflict associated with an anthropogenic food source. We built a Bayesian hierarchical model based on 14 years of aerial survey data to estimate the weekly number and distribution of polar bears on the coast of northern Alaska in autumn. We then used the model to predict how effective two management options for handling subsistence-harvested whale remains in the community of Kaktovik, Alaska might be. The distribution of bears on shore was most strongly influenced by the presence of whale carcasses and to a lesser extent sea ice and onshore habitat conditions. The numbers of bears on shore were related to sea ice conditions. The two management strategies for handling the whale carcasses reduced the estimated number of bears near Kaktovik by > 75%. By considering multiple factors associated with the onshore distribution and abundance of polar bears we discerned what role human activities played in where bears occur and how successful efforts to manage the whale carcasses might be for reducing human-polar bear conflict.

Alaska

Survey-based assessment of the frequency and potential impacts of recreation on polar bears

Conservation plans for polar bears ( Ursus maritimus ) typically cannot prescribe management actions to address their primary threat: sea ice loss associated with climate warming. However, there may be other stressors that compound the negative effects of sea ice loss which can be mitigated. For example, Arctic tourism has increased concurrent with polar bears increasingly using terrestrial habitats, which creates the potential for increased human-bear interactions. Little is known about the types, frequency, or potential impacts of recreation. We conducted a Delphi survey among experts who live and work in polar bear habitats, followed by an internet-based survey to which 47 managers, tour operators, community members, and scientists contributed. Participants identified viewing-based recreation as increasing and affecting the largest proportion of bears within subpopulationsthat come ashore during the ice-free season. Survey respondents suggested that negative effects of viewing, including displacement and habituation, could be reduced by restricting human use areas and distances between bears and people. Killing of bears in defense was associated more with camping or hunting for other species than other recreations, and may be mitigated with deterrents. Snowmobiling was the most common recreation across the polar bears' range, and reportedly caused some den abandonment and displacement. However, respondents estimated that <10% of polar bears are exposed to most types of recreation and <50% surmised any negative impacts. Nevertheless, mitigating some of the negative impacts identified in this study may become increasingly important as polar bears cope with sea ice loss.

Biological Conservation

Validating the performance of occupancy models for estimating habitat use and predicting the distribution of highly-mobile species: A case study using the American black bear

Occupancy models have become a valuable tool for estimating wildlife-habitat relationships and for predicting species distributions. Highly-mobile species often violate the assumption that sampling units are geographically closed shifting the probability of occupancy to be interpreted as the probability of use. We used occupancy models, in conjunction with noninvasive sampling, to estimate habitat use and predict the distribution of a highly-mobile carnivore, the American black bear ( Ursus americanus ) in New Mexico, USA. The top model indicated that black bears use areas with higher primary productivity and fewer roads. The predictive performance of such models is rarely validated with independent data, so we validated our model predictions with 2-independent datasets. We first assessed the correlation between predicted and observed habitat use for 28 telemetry-collared bears in the Jemez Mountains. Predicted habitat use was positively correlated with observed use for all 3 years (2012: ρ = 0.81; 2013: ρ = 0.87; 2014: ρ = 0.90). We then predicted the probability of use within a cell where a bear mortality was documented using 2043 mortality locations from sport harvest, depredation, and vehicle collisions. The probability of habitat use at a mortality location was also positively correlated with observed use by the species (2012: ρ = 0.74; 2013: ρ = 0.89; 2014: ρ = 0.93). Our validation procedure supports the notion that occupancy models can be an effective tool for estimating habitat use and predicting the distribution of highly-mobile species when the assumption of geographic closure has been violated. Our findings may be of interest to studies that are estimating habitat use for highly-mobile species that are secretive or rare, difficult to capture, or expensive to monitor with other more intensive methods.

New Mexico

Grizzly bear movement models predict habitat use for nearby populations

Conservation planning and decision-making can be enhanced by ecological models that reliably transfer to times and places beyond those where models were developed. Transferrable models can be especially helpful for species of conservation concern, such as grizzly bears ( Ursus arctos ). Currently, only four grizzly bear populations remain in the contiguous United States. We evaluated transferability of previously derived individual-based, integrated step selection functions (iSSFs) developed from GPS-collared grizzly bears in the Northern Continental Divide Ecosystem by applying them within the nearby Selkirk (SE), Cabinet-Yaak (CYE), and Greater Yellowstone Ecosystems (GYE). We simulated 100 replicates of 5000 steps for each iSSF in each ecosystem, summarized relative use into 10 equal-area classes for each sex, and overlaid GPS locations from bears in the SE, CYE, and GYE on resulting maps. Spearman rank correlations between numbers of locations and class rank were ≥ 0.96 within each study area, indicating models were highly predictive of grizzly bear space use in these nearby populations. Assessment of models using smaller subsets of data in space and time demonstrated generally high predictive accuracy for females. Although generally high across space and time, predictive accuracy for males was low within some watersheds and in summer within the SE and CYE, potentially due to seasonal effects, vegetation, and food assemblage differences. Altogether, these results demonstrated high transferability of our models to landscapes in the Northern Rocky Mountains, suggesting they may be used to evaluate habitat suitability and connectivity throughout the region to benefit conservation planning.

Idaho, Montana, Washington, Wyoming

Genetic architecture and evolution of color variation in American black bears

Color variation is a frequent evolutionary substrate for camouflage in small mammals, but the underlying genetics and evolutionary forces that drive color variation in natural populations of large mammals are mostly unexplained. The American black bear, Ursus americanus ( U. americanus ), exhibits a range of colors including the cinnamon morph, which has a similar color to the brown bear, U. arctos , and is found at high frequency in the American southwest. Reflectance and chemical melanin measurements showed little distinction between U. arctos and cinnamon U. americanus individuals. We used a genome-wide association for hair color as a quantitative trait in 151 U. americanus individuals and identified a single major locus (p < 10 −13 ). Additional genomic and functional studies identified a missense alteration (R153C) in Tyrosinase-related protein 1 ( TYRP1 ) that likely affects binding of the zinc cofactor, impairs protein localization, and results in decreased pigment production. Population genetic analyses and demographic modeling indicated that the R153C variant arose 9.36 kya in a southwestern population where it likely provided a selective advantage, spreading both northwards and eastwards by gene flow. A different TYRP1 allele, R114C, contributes to the characteristic brown color of U. arctos but is not fixed across the range.

Current Biology

Simulating realistic predator signatures in quantitative fatty acid signature analysis

Diet estimation is an important field within quantitative ecology, providing critical insights into many aspects of ecology and community dynamics. Quantitative fatty acid signature analysis (QFASA) is a prominent method of diet estimation, particularly for marine mammal and bird species. Investigators using QFASA commonly use computer simulation to evaluate statistical characteristics of diet estimators for the populations they study. Similar computer simulations have been used to explore and compare the performance of different variations of the original QFASA diet estimator. In both cases, computer simulations involve bootstrap sampling prey signature data to construct pseudo-predator signatures with known properties. However, bootstrap sample sizes have been selected arbitrarily and pseudo-predator signatures therefore may not have realistic properties. I develop an algorithm to objectively establish bootstrap sample sizes that generates pseudo-predator signatures with realistic properties, thereby enhancing the utility of computer simulation for assessing QFASA estimator performance. The algorithm also appears to be computationally efficient, resulting in bootstrap sample sizes that are smaller than those commonly used. I illustrate the algorithm with an example using data from Chukchi Sea polar bears ( Ursus maritimus ) and their marine mammal prey. The concepts underlying the approach may have value in other areas of quantitative ecology in which bootstrap samples are post-processed prior to their use.

Ecological Informatics

Incremental evolution of modeling a prognosis for polar bears in a rapidly changing Arctic

Updating predictions of the response of high-profile, at-risk species to climate change and anthropogenic stressors is vital for informing effective conservation action. Here, we review two prior generations of Bayesian network probability models predicting changes in global polar bear ( Ursus maritimus ) population status, and provide a contemporary update based on recent research findings and sea-ice projections by newer climate models. We compare predictions of polar bear population response from all 3 models among four circumpolar Arctic ecoregions, using sea ice projections based on three IPCC greenhouse gas emissions scenarios (SSP2.6, 4.5, 8.5). Consistent with the previous two model generations, polar bears will continue to experience increasing probability of declining or greatly declining populations throughout the 21st century, varying by emission scenario. Populations within the Polar Basin Divergent Ice Ecoregion have the highest predicted probability of declines, but predictions were slightly less dire relative to the previous model generation. Most of the influence, denoted by model sensitivity analysis, is from expected degradation and loss of sea ice and reduced access to marine prey. The lack of terrestrial prey adequate to substitute for loss of access to marine prey, as well as human-caused bear morality associated with hunting and defense of life and property encountered when polar bears are increasingly forced ashore also contributed to predicted declines. Although some tidewater glacial fjords and other localized onshore resources may provide local refugia, their benefit is transient. Our findings continue to inform priorities for inventory, monitoring, and research needs, and suggest that similar updates to models of other at-risk species can capitalize on the comparison framework we present here.

Ecological Indicators

Giardia and Cryptosporidium in resident wildlife species in Arctic Alaska

Giardia and Cryptosporidium are zoonotic protozoan parasites that can infect humans and other taxa, including wildlife, often causing gastrointestinal illness. Both have been identified as One Health priorities in the Arctic, where climate change is expected to influence the distribution of many wildlife and zoonotic diseases, but little is known about their prevalence in local wildlife. To help fill information gaps, we collected fecal samples from four wildlife species that occur seasonally on the northern Alaska coastline or in nearshore marine waters—Arctic fox ( Vulpes lagopus ), polar bear ( Ursus maritimus ), Pacific walrus ( Odobenus rosmarus divergens ), and caribou ( Rangifer tarandus )—and used immunofluorescence assays to screen for Giardia cysts and Cryptosporidium oocysts. We detected Giardia cysts in 18.3% and Cryptosporidium oocysts in 16.5% of Arctic foxes ( n = 109), suggesting that foxes may be potentially important hosts in this region. We also detected Giardia cysts in a single polar bear (12.5%; n = 8), which to our knowledge represents the first such report for this species. Neither parasite was detected in walruses or caribou.

Food and Waterborne Parasitology

Foraging behavior of pileated woodpeckers in partial cut and uncut bottomland hardwood forest

In bottomland hardwood forests, partial cutting techniques are increasingly advocated and used to create habitat for priority wildlife like Louisiana black bear ( Ursus americanus luteolus ), white-tailed deer ( Odocoileus virginianus ), and Neotropical migrants. Although partial cutting may be beneficial to some species, those that use dead wood may be negatively affected since large diameter and poor quality trees (deformed, moribund, or dead) are rare, but normally targeted for removal. On the other hand, partial cutting can create dead wood if logging slash is left on-site. We studied foraging behavior of pileated woodpeckers ( Dryocopus pileatus ) in one- and two-year-old partial cuts designed to benefit priority species and in uncut forest during winter, spring, and summer of 2006 and 2007 in Louisiana. Males and females did not differ in their use of tree species, dbh class, decay class, foraging height, use of foraging tactics or substrate types; however, males foraged on larger substrates than females. In both partial cut and uncut forest, standing live trees were most frequently used (83% compared to 14% for standing dead trees and 3% for coarse woody debris); however, dead trees were selected (i.e. used out of proportion to availability). Overcup oak ( Quercus lyrata ) and bitter pecan ( Carya aquatica ) were also selected and sugarberry ( Celtis laevigata ) avoided. Pileated woodpeckers selected trees >= 50 cm dbh and avoided trees in smaller dbh classes (10-20 cm). Density of selected foraging substrates was the same in partial cut and uncut forest. Of the foraging substrates, woodpeckers spent 54% of foraging time on live branches and boles, 37% on dead branches and boles, and 9% on vines. Of the foraging tactics, the highest proportion of foraging time was spent excavating (58%), followed by pecking (14%), gleaning (14%), scaling (7%), berry-eating (4%), and probing (3%). Woodpecker use of foraging tactics and substrates, and foraging height and substrate diameter did not differ between recent partial cut and uncut forest. Partial cutting designed to improve or maintain habitat for priority wildlife did not affect pileated woodpecker foraging behavior or availability of selected trees compared to uncut forest in the short term.

Forest Ecology and Management

Long-term variation in polar bear body condition and maternal investment relative to a changing environment

In the Arctic, warming air and ocean temperatures have resulted in substantial changes to sea ice, which is primary habitat for polar bears ( Ursus maritimus ). Reductions in extent, duration, and thickness have altered sea ice dynamics, which influences the ability of polar bears to reliably access marine mammal prey. Because nutritional condition is closely linked to population vital rates, a progressive decline in access to prey or an increase in the energetic cost of accessing prey has the potential to adversely affect polar bear population dynamics. We examined long-term (1983–2015) patterns of spring body condition (indexed using residual body mass) and maternal investment (i.e., litter mass of cubs-of-the-year and yearlings; COY and YRL) of polar bears from Alaska’s southern Beaufort Sea to evaluate potential relationships with regional- and circumpolar-scale sea ice conditions and atmospheric patterns. The length of the summer open-water (OW) season (i.e., the period of time the sea ice is mostly absent from the continental shelf) increased at a rate of 18 days decade -1 over the study period. However, the OW season duration was not a strong determinant of spring residual body mass or litter mass. Residual body mass of independent (i.e., subadults and adults) female bears varied relative to age class, reproductive status, and the strength of the prior winter’s Arctic Oscillation (i.e., a circumpolar-scale mode of climate variability driven by long-term atmospheric patterns). Spring residual mass of independent males varied with age class and variation in wind speed (i.e., regional-scale short-term atmospheric patterns) during the winter of the year preceding capture. Over the study period, mean annual body mass of adult females unaccompanied by COY declined by 4 kg/ decade -1 , while no temporal trends were evident in the mean annual body mass of adult females with COY, adult males, and subadults. Litter mass of COY varied relative to capture date, maternal age class and mass, litter size, and year of capture. Litter mass of YRL varied with capture date, maternal age class and mass, litter size, variation in winter wind speed (the year of and year preceding capture), and the strength of the prior winter’s Arctic Oscillation. Mean annual litter mass of COY decreased at a rate of 2.6 kg decade -1 and declined 0.68 kg for every 10 kg reduction in maternal mass. No trend was evident in the mean annual litter mass of yearlings. These findings suggest a nuanced response of the southern Beaufort Sea polar bears to environmental change, where some demographic groups (e.g., adult males and subadults) are presently more resilient than others to changes in the Arctic marine ecosystem.

Alaska

The need to step-up monitoring of Asian bears

Many wildlife species are threatened in Asia, including the five species of terrestrial bears (Asiatic black, Ursus thibetanus ; brown, U. arctos ; sloth, Melursus ursinus ; sun, Helarctos malayanus ; giant panda, Ailuropoda melanoleuca ): many populations of these bears are thought to be declining or imperiled by small population size. Here our aim is to document how population assessments have been conducted for bears in Asia. We searched the literature and identified 102 studies published during 1999–2021 that investigated the status of an Asian bear population; these occurred in 24 of the 32 bear range countries in Asia. At the most basic level, 11% of studies verified presence of bears in places where they were not known to exist. The most common objective (53% of papers) was a distribution map, often derived from presence locations in a habitat-based model. Occupancy studies (15%) used temporal (time stamps on images from cameras) or spatial (transect segments) replicates, but tended to focus on “use”, so detector spacing was sometimes not appropriate for occupancy. Purported population indices, such as sign density or camera trap encounter rates, were reported in 16% of studies. One third of studies provided a population estimate, but only 10 studies in two decades used a rigorous method (e.g., mark–recapture). Sign surveys and interviews were the most common methods for determining bear presence, and local interviews were heavily relied upon for assessing population trend. Camera trapping has become increasingly prevalent, but only one study obtained a population estimate using photographs to distinguish natural individual markings. Only three studies used hair traps to obtain DNA-based population estimates, and three other studies obtained population estimates from DNA in scats. Just three studies quantitatively measured change in population size or occupancy over time, and none of these showed a decline. Unique rangewide sign surveys of giant pandas showed significant geographic expansion. The opinions of experts and local people, now heavily relied upon for population assessments, are not reliable or sensitive enough for monitoring. Quantitative population assessments are desirable to direct conservation actions toward the most perilous situations, and provide a means to gauge the effectiveness of conservation actions. This paper demonstrates the paucity of rigorous monitoring of Asian bears, and leads off a series of papers that propose improved methods for assessing distribution, occupancy, and density

Global Ecology and Conservation

Observed and forecasted changes in land use by polar bears in the Beaufort and Chukchi Seas, 1985–2040

Monitoring changes in the distribution of large carnivores is important for managing human safety and supporting conservation. Throughout much of their range, polar bears ( Ursus maritimus ) are increasingly using terrestrial habitats in response to Arctic sea ice decline. Their increased presence in coastal areas has implications for bear-human conflict, inter-species interactions, and polar bear health and survival. We examined observed trends in land use over three decades by polar bears in the southern Beaufort Sea (SB) and Chukchi Sea (CS) where bears have traditionally spent most of the year on the sea ice. Using data from 408 adult females fitted with satellite radio-collars, we examined trends in the annual proportion of bears coming onshore (hereafter referred to as “percent of bears”) during the summer for ≥21 days, arrival and departure dates, duration spent onshore and relationships with sea ice metrics. We then estimated future land use through 2040 by extrapolating trends and by combining observed relationships between land use and sea ice with projections of future sea ice from an ensemble of earth system models. The observed percent of bears summering onshore and their duration onshore was correlated with the percent of open water that occurred within their population’s range between July and October. As sea ice declined, the percent of bears summering onshore increased from ~5 to 30% in the SB and ~10 to 50% in the CS and duration onshore increased by >30 days to 60–70 days in both populations. Using a range of greenhouse gas emission scenarios and adjustments for faster than forecasted sea ice loss we estimated that 50-62% of SB and 79-88% of CS bears will spend 90–108 and 110–126 days onshore during summer in the SB and CS, respectively, by 2040. Sea ice projections varied little between greenhouse gas emission scenarios prior to 2040 but diverged thereafter. Observed and forecasted increases in polar bear land occupancy puts more bears in proximity to human activities and settlements for longer durations while extending the lack of access to their primary prey. Because human conflict is one of the primary factors affecting the conservation of large carnivores worldwide, mitigation of bear-human interactions on land will be an increasingly important component of polar bear conservation.

Alaska

A unified approach to long-term population monitoring of grizzly bears in the Greater Yellowstone Ecosystem

Long-term wildlife research and monitoring programs strive to maintain consistent data collections and analytical methods. Incorporating new techniques is important but can render data sets incongruent and limit their potential to discern trends in demographic parameters. Integrated population models (IPMs) can address these limitations by combining data sources that may span different periods into a unified statistical framework while providing a holistic view of population dynamics. We developed an IPM in a Bayesian framework for grizzly bears ( Ursus arctos ) in the Greater Yellowstone Ecosystem. We coupled demographic data with multiple, independent population count data to link annual changes in abundance with vital rates over 4 decades (1983–2023). Abundance increased threefold from an estimated 270 individuals in 1984 to 1030 individuals in 2023. Parameter estimates indicated survival of bears ≥2 years of age was high, contributing to robust population growth during the 1980s (λ = 1.023 [50 % interquartile range = 0.993–1.082]) and 1990s (λ = 1.064 [1.023–1.103]). A slowing of population growth started around 2000 (2000s: λ = 1.030 [0.989–1.068]) and continued into the 2010s (λ = 1.021 [0.985–1.057]), due primarily to reductions in survival of bears <2 years of age. These findings corroborate previous research that identified density-dependent effects as a likely cause. The IPM framework provided greater certainty and understanding regarding the dynamic demographic characteristics of the population and serves as a powerful monitoring tool for this long-lived species. Implementation of the IPM allows timely dissemination of demographic data to help inform adaptive management strategies and policy decisions necessary for the continued management and conservation of this population. This robust and flexible monitoring system allows scientists to investigate the effects of a changing ecosystem on population dynamics, incorporate new data sources and statistical models, and respond to changes in monitoring needs for the population. We highlight the efficacy of the IPM in estimating and tracking demographic parameters for a long-lived species, while accommodating shifts in monitoring techniques and data collections typical of long-term wildlife conservation programs worldwide.

Idaho, Montana, Wyoming

High-resolution U-series dates from the Sima de los Huesos hominids yields 600 +∞ -66 : implications for the evolution of the early Neanderthal lineage

The Sima de los Huesos site of the Atapuerca complex near Burgos, Spain contains the skeletal remains of at least 28 individuals in a mud-breccia underlying an accumulation of the Middle Pleistocene cave bear (Ursus deningeri). We report here on new high-precision dates on the recently discovered speleothem SRA-3 overlaying human bones within the Sima de los Huesos. Earlier analyses of this speleothem by TIMS (thermal-ionization mass-spectrometry) showed the lower part to be indistinguishable from internal isotopic equilibrium at the precision of the TIMS instrumentation used, yielding minimum age of 350 kyr (kyr = 103 yr before present). Reanalysis of six samples of SRA-3 by inductively-coupled plasma-multicollector mass-spectrometry (ICP-MS) produced high-precision analytical results allowing calculation of finite dates. The new dates cluster around 600 kyr. A conservative conclusion takes the lower error limit ages as the minimum age of the speleothem, or 530 kyr. This places the SH hominids at the very beginnings of the Neandertal evolutionary lineage.

Atapuerca

Hibernating bears as a model for preventing disuse osteoporosis

The hibernating bear is an excellent model for disuse osteoporosis in humans because it is a naturally occurring large animal model. Furthermore, bears and humans have similar lower limb skeletal morphology, and bears walk plantigrade like humans. Black bears (Ursus americanus) may not develop disuse osteoporosis during long periods of disuse (i.e. hibernation) because they maintain osteoblastic bone formation during hibernation. As a consequence, bone volume, mineral content, porosity, and strength are not adversely affected by annual periods of disuse. In fact, cortical bone bending strength has been shown to increase with age in hibernating black bears without a significant change in porosity. Other animals require remobilization periods 2-3 times longer than the immobilization period to recover the bone lost during disuse. Our findings support the hypothesis that black bears, which hibernate for as long as 5-7 months annually, have evolved biological mechanisms to mitigate the adverse effects of disuse on bone porosity and strength. ?? 2005 Elsevier Ltd. All rights reserved.

Journal of Biomechanics

Influences of landscape heterogeneity on home-range sizes of brown bears

Animal space use is influenced by many factors and can affect individual survival and fitness. Under optimal foraging theory, individuals use landscapes to optimize high-quality resources while minimizing the amount of energy used to acquire them. The spatial resource variability hypothesis states that as patchiness of resources increases, individuals use larger areas to obtain the resources necessary to meet energetic requirements. Additionally, under the temporal resource variability hypothesis, seasonal variation in available resources can reduce distances moved while providing a variety of food sources. Our objective was to determine if seasonal home ranges of brown bears ( Ursus arctos ) were influenced by temporal availability and spatial distribution of resources and whether individual reproductive status, sex, or size (i.e., body mass) mediated space use. To test our hypotheses, we radio collared brown bears ( n = 32 [9 male, 23 female]) in 2014–2016 and used 18 a priori selected linear models to evaluate seasonal utilization distributions (UD) in relation to our hypotheses. Our top-ranked model by AIC c , supported the spatial resource variability hypothesis and included percentage of like adjacency (PLADJ) of all cover types (P < 0.01), reproductive class (P > 0.17 for males, solitary females, and females with dependent young), and body mass (kg; P = 0.66). Based on this model, for every percentage increase in PLADJ, UD area was predicted to increase 1.16 times for all sex and reproductive classes. Our results suggest that landscape heterogeneity influences brown bear space use; however, we found that bears used larger areas when landscape homogeneity increased, presumably to gain a diversity of food resources. Our results did not support the temporal resource variability hypothesis, suggesting that the spatial distribution of food was more important than seasonal availability in relation to brown bear home range size.

Alaska