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Interspecific and intraspecific mitochondrial DNA variation in North American bears (Ursus)

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf01732759openalex-snapshot
The use of restriction endonucleases to measure mitochondrial DNA sequence relatedness in natural populations
inferredcites →https://doi.org/10.1007/bf02257369openalex-snapshot
Demographic influences on mitochondrial DNA lineage survivorship in animal populations
inferredcites →https://doi.org/10.1016/b978-0-12-398760-0.50026-2openalex-snapshot
PHYLOGENETIC RELATIONSHIPS OF MITOCHONDRIAL DNA UNDER VARIOUS DEMOGRAPHIC MODELS OF SPECIATION11Work was supported by an NIH predoctoral fellowship to JEN, and by NSF Grant BSR-8217291.
inferredcites →https://doi.org/10.1016/s0076-6879(80)65051-4openalex-snapshot
[49] Rapid DNA isolations for enzymatic and hybridization analysis
inferredcites →https://doi.org/10.1073/pnas.76.10.5269openalex-snapshot
Mathematical model for studying genetic variation in terms of restriction endonucleases.
inferredcites →https://doi.org/10.1073/pnas.76.12.6694openalex-snapshot
Mitochondrial DNA clones and matriarchal phylogeny within and among geographic populations of the pocket gopher, Geomys pinetis.
inferredcites →https://doi.org/10.1073/pnas.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.83.24.9576openalex-snapshot
Mitochondrial DNA analysis of hybridization between sympatric white-tailed deer and mule deer in west Texas.
inferredcites →https://doi.org/10.1073/pnas.87.5.1772openalex-snapshot
Large sequence divergence among mitochondrial DNA genotypes within populations of eastern African black-backed jackals.
inferredcites →https://doi.org/10.1093/genetics/105.3.681openalex-snapshot
MITOCHONDRIAL DNA EVOLUTION IN MICE
inferredcites →https://doi.org/10.1093/genetics/97.1.125openalex-snapshot
INTRA- AND INTERSPECIFIC VARIATION OF THE MITOCHONDRIAL GENOME IN RATTUS NORVEGICUS AND RATTUS RATTUS : RESTRICTION ENZYME ANALYSIS OF VARIANT MITOCHONDRIAL DNA MOLECULES AND THEIR EVOLUTIONARY RELATIONSHIPS
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040301openalex-snapshot
Mitochondrial DNA differentiation during the speciation process in Peromyscus.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040339openalex-snapshot
A comparative description of mitochondrial DNA differentiation in selected avian and other vertebrate genera.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040517openalex-snapshot
Relationships between gene trees and species trees.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040651openalex-snapshot
Molecular distance and divergence time in carnivores and primates.
inferredcites →https://doi.org/10.1098/rstb.1986.0011openalex-snapshot
Mitochondrial DNA and the evolutionary genetics of higher animals
inferredcites →https://doi.org/10.1111/j.1095-8312.1985.tb02048.xopenalex-snapshot
Mitochondrial DNA and two perspectives on evolutionary genetics
inferredcites →https://doi.org/10.1111/j.1558-5646.1967.tb03411.xopenalex-snapshot
PHYLOGENETIC ANALYSIS: MODELS AND ESTIMATION PROCEDURES
inferredcites →https://doi.org/10.1111/j.1558-5646.1983.tb05509.xopenalex-snapshot
EXTENSIVE GENETIC VARIATION IN MITOCHONDRIAL DNA'S AMONG GEOGRAPHIC POPULATIONS OF THE DEER MOUSE,PEROMYSCUS MANICULATUS
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb04208.xopenalex-snapshot
PHYLOGEOGRAPHIC PATTERNS IN MITOCHONDRIAL DNA OF THE DESERT TORTOISE ( XEROBATES AGASSIZI ), AND EVOLUTIONARY RELATIONSHIPS AMONG THE NORTH AMERICAN GOPHER TORTOISES
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb04228.xopenalex-snapshot
MOLECULAR GENETIC-DISTANCE ESTIMATES AMONG THE URSIDAE AS INDICATED BY ONE- AND TWO-DIMENSIONAL PROTEIN ELECTROPHORESIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb03829.xopenalex-snapshot
MITOCHONDRIAL GENE TREES AND THE EVOLUTIONARY RELATIONSHIP OF MALLARD AND BLACK DUCKS
inferredcites →https://doi.org/10.1111/j.1558-5646.1991.tb05279.xopenalex-snapshot
PHYLOGENETIC RELATIONSHIPS OF NORTH AMERICAN URSIDS BASED ON ANALYSIS OF MITOCHONDRIAL DNA
inferredcites →https://doi.org/10.1111/j.1601-5223.1979.tb01636.xopenalex-snapshot
Electrophoretic variation in large mammals: I. The polar bear, Thalarctos maritimus
inferredcites →https://doi.org/10.1111/j.1751-8369.1983.tb00735.xopenalex-snapshot
Low protein variability and genetic similarity between populations of the polar bear (Ursus maritimus)
inferredcites →https://doi.org/10.1126/science.155.3760.279openalex-snapshot
Construction of Phylogenetic Trees
inferredcites →https://doi.org/10.1126/science.3576198openalex-snapshot
Gene Flow and the Geographic Structure of Natural Populations
inferredcites →https://doi.org/10.1139/z91-179openalex-snapshot
Mitochondrial and nuclear genetic relationships of deer (Odocoileus spp.) in western North America
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.001413openalex-snapshot
EVOLUTION OF ANIMAL MITOCHONDRIAL DNA: RELEVANCE FOR POPULATION BIOLOGY AND SYSTEMATICS
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.002421openalex-snapshot
INTRASPECIFIC PHYLOGEOGRAPHY: The Mitochondrial DNA Bridge Between Population Genetics and Systematics
inferredcites →https://doi.org/10.14430/arctic3446openalex-snapshot
Postglacial Distribution Patterns of Mammals in the Southern Coastal Regions of Alaska
inferredcites →https://doi.org/10.2307/1380937openalex-snapshot
Genetic Variation in Black Bears from the Great Smoky Mountains National Park
inferredcites →https://doi.org/10.2307/3059openalex-snapshot
Mammals of the World
inferredcites →https://doi.org/10.2307/3534169openalex-snapshot
Mammals of the World
inferredcites →https://doi.org/10.2307/3669094openalex-snapshot
The Mammals of North America
inferredcites →https://doi.org/10.2307/3801243openalex-snapshot
Genetic Relationships between Mule Deer and White-Tailed Deer in Montana
inferredcites →https://doi.org/10.2307/3872840openalex-snapshot
Biochemical Variation in the Black Bear
inferredcites →https://doi.org/10.2307/3872922openalex-snapshot
Seasonal Movements of Adult Female Polar Bears in the Bering and Chukchi Seas

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Examining the sensitivity of molecular species delimitations to the choice of mitochondrial marker
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Evolutionary History of Polar and Brown Bears
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Admixture in Mammals and How to Understand Its Functional Implications
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Hybridization in human evolution: Insights from other organisms
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Contribution of hybridization between polar bears and grizzly bears to polar bear extinction
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Molecular phylogenetics and historical biogeography of east African chimpanzees
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Rapid Radiation Events in the Family Ursidae Indicated by Likelihood Phylogenetic Estimation from Multiple Fragments of mtDNA
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An Ice Age Refugium for Large Mammals in the Alexander Archipelago, Southeastern Alaska
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Polar Bear Taxonomy and Evolution
inferred← citeshttps://doi.org/10.1007/s10592-006-9192-zopenalex-snapshot
Genetic structure of American black bears in the desert southwest of North America: conservation implications for recolonization
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Biological response to climate change in the Arctic Ocean: the view from the past
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Population Structure and Dynamics
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Population Structure and Dynamics
inferred← citeshttps://doi.org/10.1016/b978-012701235-3/50009-xopenalex-snapshot
Polar Bear
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The role of Pleistocene glaciations in shaping the evolution of polar and brown bears. Evidence from a critical review of mitochondrial and nuclear genome analyses
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Ancient Hybridization and an Irish Origin for the Modern Polar Bear Matriline
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112870openalex-snapshot
Population-genomics reveals a dual ancestry of grizzly bears
inferred← citeshttps://doi.org/10.1016/j.quascirev.2010.11.023openalex-snapshot
Late-Quaternary biogeographic scenarios for the brown bear (Ursus arctos), a wild mammal model species
inferred← citeshttps://doi.org/10.1017/9781108692571openalex-snapshot
Bears of the World
inferred← citeshttps://doi.org/10.1017/9781108692571.001openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1017/9781108692571.002openalex-snapshot
Systematics, Evolution, and Genetics of Bears
inferred← citeshttps://doi.org/10.1017/9781108692571.003openalex-snapshot
Mating Strategies
inferred← citeshttps://doi.org/10.1017/9781108692571.004openalex-snapshot
Interspecific Interactions between Brown Bears, Ungulates, and Other Large Carnivores
inferred← citeshttps://doi.org/10.1017/9781108692571.005openalex-snapshot
Adaptations and Competitive Interactions of Tropical Asian Bear Species Define Their Biogeography: Past, Present, and Future
inferred← citeshttps://doi.org/10.1017/9781108692571.006openalex-snapshot
Remarkable Adaptations of the American Black Bear Help Explain Why it is the Most Common Bear: A Long-Term Study from the Center of its Range
inferred← citeshttps://doi.org/10.1017/9781108692571.007openalex-snapshot
Giant Panda (Ailuropoda melanoleuca)
inferred← citeshttps://doi.org/10.1017/9781108692571.008openalex-snapshot
Andean Bear (Tremarctos ornatus)
inferred← citeshttps://doi.org/10.1017/9781108692571.009openalex-snapshot
Sun Bear (Helarctos malayanus)
inferred← citeshttps://doi.org/10.1017/9781108692571.010openalex-snapshot
Sloth Bear ( Melursus ursinus )
inferred← citeshttps://doi.org/10.1017/9781108692571.011openalex-snapshot
Asiatic Black Bear (Ursus thibetanus)
inferred← citeshttps://doi.org/10.1017/9781108692571.012openalex-snapshot
American Black Bear (Ursus americanus)
inferred← citeshttps://doi.org/10.1017/9781108692571.013openalex-snapshot
Brown Bear (Ursus arctos; Eurasia)
inferred← citeshttps://doi.org/10.1017/9781108692571.014openalex-snapshot
Brown Bear (Ursus arctos; North America)
inferred← citeshttps://doi.org/10.1017/9781108692571.015openalex-snapshot
Polar Bear (Ursus maritimus)
inferred← citeshttps://doi.org/10.1017/9781108692571.016openalex-snapshot
Human–Bear Conflicts at the Beginning of the Twenty-First Century: Patterns, Determinants, and Mitigation Measures
inferred← citeshttps://doi.org/10.1017/9781108692571.017openalex-snapshot
Principles of Human–Bear Conflict Management in Challenging Environments
inferred← citeshttps://doi.org/10.1017/9781108692571.018openalex-snapshot
Patterns of Bear Attacks on Humans, Factors Triggering Risky Scenarios, and How to Reduce Them
inferred← citeshttps://doi.org/10.1017/9781108692571.019openalex-snapshot
Effects of Human Disturbance on Brown Bear Behavior
inferred← citeshttps://doi.org/10.1017/9781108692571.020openalex-snapshot
Bears in Human-Modified Landscapes: The Case Studies of the Cantabrian, Apennine, and Pindos Mountains
inferred← citeshttps://doi.org/10.1017/9781108692571.021openalex-snapshot
Conservation and Management of Bears
inferred← citeshttps://doi.org/10.1017/9781108692571.022openalex-snapshot
How Is Climate Change Affecting Polar Bears and Giant Pandas?
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Managing for Interpopulation Connectivity of the World’s Bear Species
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Ex SituConservation of Bears: Roles, Status, and Management
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The Challenge of Brown Bear Management in Hokkaido, Japan
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Potential Ecological Corridors for Remnant Asiatic Black Bear Populations and its Subpopulations Linked to Management Units in Japan
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Captive Bears in Asia: Implications for Animal Welfare and Conservation
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Human Dimensions of Asiatic Black Bear Conflicts and Management in Japan
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Ecological and Social Dimensions of Sloth Bear Conservation in Sri Lanka
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Plate Section (PDF Only)
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Foreword
inferred← citeshttps://doi.org/10.1017/9781108692571.032openalex-snapshot
Frontispiece
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Phylogenetic units and currencies above and below the species level
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Building large trees by combining phylogenetic information: a complete phylogeny of the extant Carnivora (Mammalia)
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Non‐invasive genotyping of the endangered Apennine brown bear: a case study not to let one's hair down
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Mitochondrial DNA Phylogeography and Comparative Cytogenetics of the Springhare, Pedetes capensis (Mammalia: Rodentia)
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Mitochondrial DNA sequence divergence among some west European brown bear (Ursus arctos L.) populations. Lessons for conservation
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Range-wide whole-genome resequencing of the brown bear reveals drivers of intraspecies divergence
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The evolutionary history of bears is characterized by gene flow across species
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Gene flow between insular, coastal and interior populations of brown bears in Alaska
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Genetic structure of the world’s polar bear populations
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Mitochondrial DNA Phylogeography of the North American Brown Bear and Implications for Conservation
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Why is the giant panda black and white?
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LOW GENETIC VARIABILITY IN THE GEOGRAPHICALLY WIDESPREAD ANDEAN CONDOR
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Genetic relationships of grizzly bears (Ursus arctos) in the Prudhoe Bay region of Alaska: inference from microsatellite DNA, mitochondrial DNA, and field observations
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Numt Parser: Automated identification and removal of nuclear mitochondrial pseudogenes (numts) for accurate mitochondrial genome reconstruction in Panthera
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Genetic Variation, Relatedness, and Effective Population Size of Polar Bears (Ursus maritimus) in the southern Beaufort Sea, Alaska
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Genetic Relationships of Extant Brown Bears (Ursus arctos) and Polar Bears (Ursus maritimus)
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Molecular Phylogeny and SNP Variation of Polar Bears (Ursus maritimus), Brown Bears (U. arctos), and Black Bears (U. americanus) Derived from Genome Sequences
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Mitochondrial DNA Variation in Southeastern Pre-Columbian Canids
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Molecular Phylogeography of the Brown Bear (Ursus arctos) in Northeastern Asia Based on Analyses of Complete Mitochondrial DNA Sequences
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Brown and Polar Bear Y Chromosomes Reveal Extensive Male-Biased Gene Flow within Brother Lineages
inferred← citeshttps://doi.org/10.1093/molbev/msu186openalex-snapshot
Bears in a Forest of Gene Trees: Phylogenetic Inference Is Complicated by Incomplete Lineage Sorting and Gene Flow
inferred← citeshttps://doi.org/10.1093/molbev/msy018openalex-snapshot
Genomic Evidence of Widespread Admixture from Polar Bears into Brown Bears during the Last Ice Age
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a004090openalex-snapshot
Conserved Primers for Rapid Sequencing of the Complete Mitochondrial Genome from Carnivores, Applied to Three Species of Bears
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Cryptic genetic variation and paraphyly in ravens
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Inferring species divergence times using pairwise sequential Markovian coalescent modelling and low-coverage genomic data
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Palm‐Pitviper (Bothriechis) Phylogeny, mtDNA, and Consilience
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Microsatellite analysis of genetic variation in black bear populations
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Microsatellite analysis of population structure in Canadian polar bears
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Problems with the claim of ecotype and taxon status of the wolf in the Great Lakes region
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Building large trees by combining phylogenetic information: a complete phylogeny of the extant Carnivora (Mammalia)
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Evolutionary implications of bite mechanics and feeding ecology in bears
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NORTH AMERICAN BLACK BEAR mt DNA PHYLOGEOGRAPHY: IMPLICATIONS FOR MORPHOLOGY AND THE HAIDA GWAII GLACIAL REFUGIUM CONTROVERSY
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FURTHER PERSPECTIVES ON THE HAIDA GWAII GLACIAL REFUGIUM
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COASTAL REFUGIA AND POSTGLACIAL RECOLONIZATION ROUTES: A REPLY TO DEMBOSKI, STONE, AND COOK
inferred← citeshttps://doi.org/10.1111/mec.13038openalex-snapshot
Genomic evidence of geographically widespread effect of gene flow from polar bears into brown bears
inferred← citeshttps://doi.org/10.1139/cjz-2013-0078openalex-snapshot
Genetic relationships of North American bears (Ursus) inferred from amplified fragment length polymorphisms and mitochondrial DNA sequences
inferred← citeshttps://doi.org/10.1139/cjz-2018-0113openalex-snapshot
Population genetics reveal Myotis keenii (Keen’s myotis) and Myotis evotis (long-eared myotis) to be a single species
inferred← citeshttps://doi.org/10.1139/z00-042openalex-snapshot
Phylogeography of black bears (Ursus americanus) of the Pacific Northwest
inferred← citeshttps://doi.org/10.1139/z06-039openalex-snapshot
Microsatellite DNA and mitochondrial DNA variation in polar bears (Ursus maritimus) from the Beaufort and Chukchi seas, Alaska
inferred← citeshttps://doi.org/10.1139/z08-046openalex-snapshot
Beyond mtDNA: nuclear gene flow suggests taxonomic oversplitting in the little brown bat (Myotis lucifugus)
inferred← citeshttps://doi.org/10.1139/z11-056openalex-snapshot
Microsatellite population structure of Newfoundland black bears (Ursus americanus hamiltoni)
inferred← citeshttps://doi.org/10.1139/z94-140openalex-snapshot
Mitochondrial DNA variation in Atlantic and Pacific walruses
inferred← citeshttps://doi.org/10.1139/z96-023openalex-snapshot
Mitochondrial DNA and the phylogeography of Newfoundland black bears
inferred← citeshttps://doi.org/10.1139/z96-112openalex-snapshot
Breeding populations of northern pintails have similar mitochondrial DNA
inferred← citeshttps://doi.org/10.1186/s12864-021-07915-5openalex-snapshot
First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.1287/inte.1090.0444openalex-snapshot
Rebuttal of “Polar Bear Population Forecasts: A Public-Policy Forecasting Audit”
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003345openalex-snapshot
Genomic Evidence for Island Population Conversion Resolves Conflicting Theories of Polar Bear Evolution
inferred← citeshttps://doi.org/10.1371/journal.pone.0112021openalex-snapshot
Implications of the Circumpolar Genetic Structure of Polar Bears for Their Conservation in a Rapidly Warming Arctic
inferred← citeshttps://doi.org/10.14430/arctic1236openalex-snapshot
Distribution and Abundance of Canadian Polar Bear Populations: A Management Perspective
inferred← citeshttps://doi.org/10.14430/arctic1257openalex-snapshot
Movements of a Polar Bear from Northern Alaska to Northern Greenland
inferred← citeshttps://doi.org/10.14430/arctic426openalex-snapshot
Allocating Harvests among Polar Bear Stocks in the Beaufort Sea
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In Defense of “Eve”—A Response to Templeton's Critique
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EVOLUTIONARY GENETICS AND PLEISTOCENE BIOGEOGRAPHY OF NORTH AMERICAN TREE SQUIRRELS (TAMIASCIURUS)
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Using satellite radiotelemetry data to delineate and manage wildlife populations
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A Proposal to Eliminate Redundant Terminology for Intra-Species Groups
inferred← citeshttps://doi.org/10.2307/1382713openalex-snapshot
Mitochondrial-DNA Variation and Genetic-Population Structure in Rocky Mountain Bighorn Sheep (Ovis canadensis canadensis)
inferred← citeshttps://doi.org/10.2307/1382776openalex-snapshot
Genetic Variation in a Population of Black Bears as Revealed by DNA Fingerprinting
inferred← citeshttps://doi.org/10.2307/1382828openalex-snapshot
Mitochondrial-DNA Variation among Subspecies and Populations of Sea Otters (Enhydra lutris)
inferred← citeshttps://doi.org/10.2307/1383215openalex-snapshot
Mitochondrial DNA Phylogeography of the New World Flying Squirrels (Glaucomys): Implications for Pleistocene Biogeography
inferred← citeshttps://doi.org/10.2752/089279302786992595openalex-snapshot
The origin of the dog revisited
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La conservazione dell'Orso bruno ( Ursus arctos ) in Appennino: il supporto della genetica non invasiva
inferred← citeshttps://doi.org/10.5281/zenodo.16071141openalex-snapshot
Morphological and Genetic Divergence among Alaskan Populations of Brachyramphus Murrelets
inferred← citeshttps://doi.org/10.5860/choice.44-1508openalex-snapshot
Evolutionary pathways in nature: a phylogenetic approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253656openalex-snapshot
Additional file 1 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253665openalex-snapshot
Additional file 2 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253668openalex-snapshot
Additional file 3 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253677openalex-snapshot
Additional file 4 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253680openalex-snapshot
Additional file 5 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253683openalex-snapshot
Additional file 6 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253686openalex-snapshot
Additional file 7 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253689openalex-snapshot
Additional file 8 of First core microsatellite panel identification in Apennine brown bears (Ursus arctos marsicanus): a collaborative approach
inferred← citeshttps://doi.org/10.64898/2025.12.22.695918openalex-snapshot
Notes on f 4 -ratio estimation
inferred← citeshttps://doi.org/10.70675/df452239z9000z4874zb8f5zf81822f77015openalex-snapshot
Étude des variations spatiales et temporelles du mercure en Arctique : utilisation des dents et des poils des prédateurs supérieurs comme tissus de biomonitoring
inferred← citeshttps://doi.org/10.7289/v5/tm-afsc-168openalex-snapshot
Alaska marine mammal stock assessments, 2006.
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