Search USGS⌕ Search

SEARCH · Search USGS

Results for “Ursus”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 271 records · Page 15Linked to original sources

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↗

Sex-specific variation in denning by brown bears

Denning characteristics of brown bears ( Ursus arctos ) have been described in numerous studies; however, population specific factors (i.e., landscape characteristics and climate) can greatly influence the location and timing of denning. Our objective was to evaluate den-site characteristics and denning chronology for male and female brown bears in Lake Clark National Park and Preserve, Alaska. We used maximum entropy modeling to characterize attributes of den sites and generalized linear mixed models to compare denning chronology between males and females. We located 70 den sites (19 male and 51 female) and documented den entrance ( n = 61 [15 male and 46 female]) and emergence ( n = 60 [13 male and 47 female]) dates for bears from fall 2014 to spring 2017. The best performing model for estimating probable male den-site use (AUC = 0.862) was most influenced by slope (79.5%). The most parsimonious female model (AUC = 0.910) included elevation (49.3%), slope (43.1%), and aspect (7.6%). Female brown bears on average denned at higher elevations (868, SE = 190 m) than males (762, SE = 195 m) ( F 1,73 = 4.08, P = 0.047). Additionally, female bears entered dens 8 days earlier than males (SE = 12.82; 20 and 28 October, respectively, P = 0.04), and although not significant ( P = 0.09), average female den emergence dates were 7 days (SE = 15.14) later than males. With the potential for increased human activities (i.e. resource extraction and associated access), gaining an understanding of population specific denning requirements is essential for developing future management actions. Our results provide valuable information that will allow decision makers to structure future development in a way that avoids habitats important for denning, and allows for reduced disturbance of winter den sites.

Alaska↗

Polar bear's range dynamics and survival in the Holocene

Polar bear (Ursus maritimus) is the apex predator of the Arctic, largely dependent on sea-ice. The expected disappearance of the ice cover of the Arctic seas by the mid 21st century is predicted to cause a dramatic decrease in the global range and population size of the species. To place this scenario against the backdrop of past distribution changes and their causes, we use a fossil dataset to investigate the polar bear's past distribution dynamics during the Late Glacial and the Holocene. Fossil results indicate that during the last deglaciation, polar bears were present at the southwestern margin of the Scandinavian Ice Sheet, surviving until the earliest Holocene. There are no Arctic polar bear findings from 8000–6000 years ago (8–6 ka), the Holocene's warmest period. However, fossils that date from 8-9 ka and 5–6 ka suggest that the species likely survived this period in cold refugia located near the East Siberian Sea, northern Greenland and the Canadian Archipelago. Polar bear range expansion is documented by an increase in fossils during the last 4000 years in tandem with cooling climate and expanding Arctic sea ice. The results document changes in polar bear's distribution in response to Late Glacial and Holocene Arctic temperature and sea ice trends.

Quaternary Science Reviews↗

State of knowledge on current exposure, fate and potential health effects of contaminants in polar bears from the circumpolar Arctic

The polar bear ( Ursus maritimus ) is among the Arctic species exposed to the highest concentrations of long-range transported bioaccumulative contaminants, such as halogenated organic compounds and mercury. Contaminant exposure is considered to be one of the largest threats to polar bears after the loss of their Arctic sea ice habitat due to climate change. The aim of this review is to provide a comprehensive summary of current exposure, fate, and potential health effects of contaminants in polar bears from the circumpolar Arctic required by the Circumpolar Action Plan for polar bear conservation. Overall results suggest that legacy persistent organic pollutants (POPs) including polychlorinated biphenyls, chlordanes and perfluorooctane sulfonic acid (PFOS), followed by other perfluoroalkyl compounds (e.g. carboxylic acids, PFCAs) and brominated flame retardants, are still the main compounds in polar bears. Concentrations of several legacy POPs that have been banned for decades in most parts of the world have generally declined in polar bears. Current spatial trends of contaminants vary widely between compounds and recent studies suggest increased concentrations of both POPs and PFCAs in certain subpopulations. Correlative field studies, supported by in vitro studies, suggest that contaminant exposure disrupts circulating levels of thyroid hormones and lipid metabolism, and alters neurochemistry in polar bears. Additionally, field and in vitro studies and risk assessments indicate the potential for adverse impacts to polar bear immune functions from exposure to certain contaminants.

Science of Total Environment↗

How Is climate change affecting polar bears and giant pandas?

Anthropogenic greenhouse gas emissions are the primary cause of climate change and an estimated increase of 3.7 to 4.8 °C is predicted by the year 2100 if emissions continue at current levels. Polar bears (Ursus maritimus) and giant pandas (Ailuropoda melanoleuca) provide an interesting comparison study of the impact of climate change on bear species. While polar bears and giant pandas are arguably the most distant of the bear species with regard to life histories and behavior, both are likely to be significantly impacted by the broad-scale changes to their environment that are predicted to result from climate change. Herein, we review the conservation status of both species and their habitats, and present current and predicted evidence of the impacts of a changing climate on polar bear and giant panda survival.

Book chapter↗

Status assessment of the Endangered snow leopard Panthera uncia and other large mammals in the Kyrgyz Alay , using community knowledge corrected for imperfect detection

The Endangered snow leopard Panthera uncia occurs in the Central Asian Mountains, which cover c. 2 million km 2 . Little is known about its status in the Kyrgyz Alay Mountains, a relatively narrow stretch of habitat connecting the southern and northern global ranges of the species. In 2010 we gathered information on current and past (1990, the last year of the Soviet Union) distributions of snow leopards and five sympatric large mammals across 14,000 km 2 of the Kyrgyz Alay. We interviewed 95 key informants from local communities. Across 49 400-km 2 grid cells we obtained 1,606 and 962 records of species occurrence (site use) in 1990 and 2010, respectively. The data were analysed using the multi-season site occupancy framework to incorporate uncertainty in detection across interviewees and time periods. High probability of use by snow leopards in the past was recorded in > 70% of the Kyrgyz Alay. Between the two sampling periods 39% of sites showed a high probability of local extinction of snow leopard. We also recorded high probability of local extinction of brown bear Ursus arctos (84% of sites) and Marco Polo sheep Ovis ammon polii (47% of sites), mainly in regions used intensively by people. Data indicated a high probability of local colonization by lynx Lynx lynx in 41% of the sites. Although wildlife has declined in areas of central and eastern Alay, regions in the north-west, and the northern and southern fringes appear to retain high conservation value.

Oryx↗

Carnivore re-colonisation: Reality, possibility and a non-equilibrium century for grizzly bears in the southern Yellowstone ecosystem

Most large native carnivores have experienced range contractions due to conflicts with humans, although neither rates of spatial collapse nor expansion have been well characterised. In North America, the grizzly bear (Ursus arctos) once ranged from Mexico northward to Alaska, however its range in the continental USA has been reduced by 95-98%. Under the U. S. Endangered Species Act, the Yellowstone grizzly bear population has re-colonised habitats outside Yellowstone National Park. We analysed historical and current records, including data on radio-collared bears, (1) to evaluate changes in grizzly bear distribution in the southern Greater Yellowstone Ecosystem (GYE) over a 100-year period, (2) to utilise historical rates of re-colonisation to project future expansion trends and (3) to evaluate the reality of future expansion based on human limitations and land use. Analysis of distribution in 20-year increments reflects range reduction from south to north (1900-1940) and expansion to the south (1940-2000). Expansion was exponential and the area occupied by grizzly bears doubled approximately every 20 years. A complementary analysis of bear occurrence in Grand Teton National Park also suggests an unprecedented period of rapid expansion during the last 20-30 years. The grizzly bear population currently has re-occupied about 50% of the southern GYE. Based on assumptions of continued protection and ecological stasis, our model suggests total occupancy in 25 years. Alternatively, extrapolation of linear expansion rates from the period prior to protection suggests total occupancy could take > 100 years. Analyses of historical trends can be useful as a restoration tool because they enable a framework and timeline to be constructed to pre-emptively address the social challenges affecting future carnivore recovery. ?? 2004 The Zoological Society of London.

Idaho, Montana, Wyoming↗

Regional contamination versus regional dietary differences: Understanding geographic variation in brominated and chlorinated contaminant levels in polar bears

The relative contribution of regional contamination versus dietary differences to geographic variation in polar bear ( Ursus maritimus ) contaminant levels is unknown. Dietary variation between Alaska, Canada, East Greenland, and Svalbard subpopulations was assessed by muscle nitrogen and carbon stable isotope (δ 15 N, δ 13 C) and adipose fatty acid (FA) signatures relative to their main prey (ringed seals). Western and southern Hudson Bay signatures were characterized by depleted δ 15 N and δ 13 C, lower proportions of C 20 and C 22 monounsaturated FAs and higher proportions of C 18 and longer chain polyunsaturated FAs. East Greenland and Svalbard signatures were reversed relative to Hudson Bay. Alaskan and Canadian Arctic signatures were intermediate. Between-subpopulation dietary differences predominated over interannual, seasonal, sex, or age variation. Among various brominated and chlorinated contaminants, diet signatures significantly explained variation in adipose levels of polybrominated diphenyl ether (PBDE) flame retardants (14−15%) and legacy PCBs (18−21%). However, dietary influence was contaminant class-specific, since only low or nonsignificant proportions of variation in organochlorine pesticide (e.g., chlordane) levels were explained by diet. Hudson Bay diet signatures were associated with lower PCB and PBDE levels, whereas East Greenland and Svalbard signatures were associated with higher levels. Understanding diet/food web factors is important to accurately interpret contaminant trends, particularly in a changing Arctic.

Environmental Science & Technology↗

Climate and reproduction of grizzly bears in Yellowstone National Park

Controversy surrounds the conflicts between the requirements of human safety and the preservation of grizzly bears ( Ursus arctos horribilis ) in western North America. It has been difficult to separate the effect of factors such as the closure of garbage dumps from that of the climate. It has also proved difficult to relate climatic data to changes in the populations of large mammals. I report here a correlation of climatic change with fluctuations in the sizes of litters of grizzly bears born in Yellowstone National Park, Wyoming, during 1958&ndash;1976. The decrease in litter sizes observed since the closure of garbage dumps seems to be largely a consequence of unfavourable weather during the periods of the final fattening of the mother, winter sleep, birth, lactation and early spring foraging. This study represents one of the few times that the effects of climate have been demonstrated for large omnivorous or carnivorous mammals.

Wyoming↗

Global change-driven use of onshore habitat impacts polar bear faecal microbiota

The gut microbiota plays a critical role in host health, yet remains poorly studied in wild species. Polar bears (Ursus maritimus), key indicators of Arctic ecosystem health and environmental change, are currently affected by rapid shifts in habitat that may alter gut homeostasis. Declining sea ice has led to a divide in the southern Beaufort Sea polar bear subpopulation such that an increasing proportion of individuals now inhabit onshore coastal regions during the open-water period (‘onshore bears’) while others continue to exhibit their typical behaviour of remaining on the ice (‘offshore bears’). We propose that bears that have altered their habitat selection in response to climate change will exhibit a distinct gut microbiota diversity and composition, which may ultimately have important consequences for their health. Here, we perform the first assessment of abundance and diversity in the faecal microbiota of wild polar bears using 16S rRNA Illumina technology. We find that bacterial diversity is significantly higher in onshore bears compared to offshore bears. The majority of unique bacterial taxa for onshore bears belonged to the phyla Proteobacteria (a proposed indicator of poor health in adult humans), whereas for offshore bears, Firmicutes (associated with adiposity) dominated. We conclude that climate-driven changes in polar bear land use are associated with distinct microbial communities. In doing so, we present the first case of global change mediated alterations in the gut microbiota of a free-roaming wild animal.

Alaska↗

Environmental and behavioral changes may influence the exposure of an Arctic apex predator to pathogens and contaminants

Recent decline of sea ice habitat has coincided with increased use of land by polar bears ( Ursus maritimus ) from the southern Beaufort Sea (SB), which may alter the risks of exposure to pathogens and contaminants. We assayed blood samples from SB polar bears to assess prior exposure to the pathogens Brucella spp ., Toxoplasma gondii , Coxiella burnetii , Francisella tularensis , and Neospora caninum , estimate concentrations of persistent organic pollutants (POPs), and evaluate risk factors associated with exposure to pathogens and POPs. We found that seroprevalence of Brucella spp . and T. gondii antibodies likely increased through time, and provide the first evidence of exposure of polar bears to C. burnetii , N. caninum , and F. tularensis . Additionally, the odds of exposure to T. gondii were greater for bears that used land than for bears that remained on the sea ice during summer and fall, while mean concentrations of the POP chlordane (ΣCHL) were lower for land-based bears. Changes in polar bear behavior brought about by climate-induced modifications to the Arctic marine ecosystem may increase exposure risk to certain pathogens and alter contaminant exposure pathways.

Alaska↗

Integrated population modeling provides the first empirical estimates of vital rates and abundance for polar bears in the Chukchi Sea

Large carnivores are imperiled globally, and characteristics making them vulnerable to extinction (e.g., low densities and expansive ranges) also make it difficult to estimate demographic parameters needed for management. Here we develop an integrated population model to analyze capture-recapture, radiotelemetry, and count data for the Chukchi Sea subpopulation of polar bears ( Ursus maritimus ), 2008–2016. Our model addressed several challenges in capture-recapture studies for polar bears by including a multievent structure reflecting location and life history states, while accommodating state uncertainty. Female breeding probability was 0.83 (95% credible interval [CRI] = 0.71–0.90), with litter sizes of 2.18 (95% CRI = 1.71–2.82) for age-zero and 1.61 (95% CRI = 1.46–1.80) for age-one cubs. Total adult survival was 0.90 (95% CRI = 0.86–0.92) for females and 0.89 (95% CRI = 0.83–0.93) for males. Spring on-ice densities west of Alaska were 0.0030 bears/km 2 (95% CRI = 0.0016–0.0060), similar to 1980s-era density estimates although methodological differences complicate comparison. Abundance of the Chukchi Sea subpopulation, derived by extrapolating density from the study area using a spatially-explicit habitat metric, was 2,937 bears (95% CRI = 1,552–5,944). Our findings are consistent with other lines of evidence suggesting the Chukchi Sea subpopulation has been productive in recent years, although it is uncertain how long this will continue given sea-ice loss due to climate change.

Scientific Reports↗

Diet-driven mercury contamination is associated with polar bear gut microbiota

The gut microbiota may modulate the disposition and toxicity of environmental contaminants within a host but, conversely, contaminants may also impact gut bacteria. Such contaminant-gut microbial connections, which could lead to alteration of host health, remain poorly known and are rarely studied in free-ranging wildlife. The polar bear ( Ursus maritimus ) is a long-lived, wide-ranging apex predator that feeds on a variety of high trophic position seal and cetacean species and, as such, is exposed to among the highest levels of biomagnifying contaminants of all Arctic species. Here, we investigate associations between mercury (THg; a key Arctic contaminant), diet, and the diversity and composition of the gut microbiota of polar bears inhabiting the southern Beaufort Sea, while accounting for host sex, age class and body condition. Bacterial diversity was negatively associated with seal consumption and mercury, a pattern seen for both Shannon and Inverse Simpson alpha diversity indices (adjusted R 2 = 0.35, F 1,18 = 8.00, P = 0.013 and adjusted R 2 = 0.26, F 1,18 = 6.04, P = 0.027, respectively). No association was found with sex, age class or body condition of polar bears. Bacteria known to either be involved in THg methylation or considered to be highly contaminant resistant, including Lactobacillales, Bacillales and Aeromonadales, were significantly more abundant in individuals that had higher THg concentrations. Conversely, individuals with higher THg concentrations showed a significantly lower abundance of Bacteroidales, a bacterial order that typically plays an important role in supporting host immune function by stimulating intraepithelial lymphocytes within the epithelial barrier. These associations between diet-acquired mercury and microbiota illustrate a potentially overlooked outcome of mercury accumulation in polar bears.

Scientific Reports↗