Museum Samples Research Articles

Colonization pathways of the northeast Atlantic by northern fulmars: a test of James Fisher’s ‘out of Iceland’ hypothesis using museum collections

When the northern fulmar expanded its northeast Atlantic breeding range from the two known colonies, Grimsey in northern Iceland and St Kilda in the Outer Hebrides, Scotland, about 350 yr ago, the geographical pattern of colonisation – initially the Faroes, then Scotland, followed by Ireland and southern Britain – led James Fisher to propose a sole Icelandic source for the colonists. However, previously‐analysed mitochondrial DNA from contemporary samples indicated a St Kildan origin for at least some colonists. If Fisher's hypothesis is correct and Iceland and not St Kilda was the source population for all of the new colonies, the Icelandic signal should be stronger in museum samples collected 100 yr ago when St Kilda was populated by people who harvested large numbers of fulmars. Patterns of genetic, specifically, nucleotide, diversity suggest an Icelandic origin for the pre‐1940 samples. St Kilda birds contained a number of closely related haplotypes whereas Grimsey, Iceland, the other putative source population, contained diverse haplotypes. These two patterns are indicative of a younger and older population, respectively. When both nuclear aldolase and mitochondrial control region sequence data from historical samples collected on the newly colonized islands were examined, they contained highly divergent haplotypes characteristic of Grimsey, not St Kilda. Comparison of mitochondrial data from samples collected in the early and late 20th century showed an interesting pattern of haplotype turnover on St Kilda. Prior to 1940 the haplotypes present on St Kilda were genetically similar to one another, yet haplotype sampling in the 1990s showed highly divergent haplotypes on the island. We propose that these new haplotypes are not the result of mutation, but immigration from other colonies in the North Atlantic.

Historic and Contemporary Mercury Exposure and Potential Risk to Yellow-Billed Loons (Gavia adamsii) Breeding in Alaska and Canada

Abstract. The Yellow-billed Loon (Gavia adamsii) is one of the rarest breeding birds in North America. Because of the small population size and patchy distribution, any stressor to its population is of concern. To determine risks posed by environmental mercury (Hg) loads, we captured 115 Yellow-billed Loons between 2002 and 2012 in the North American Arctic and sampled their blood and/or feather tissues and collected nine eggs. Museum samples from Yellow-billed Loons also were analyzed to examine potential changes in Hg exposure over time. An extensive database of published Hg concentrations and associated adverse effects in Common Loons (G. immer) is highly informative and representative for Yellow-billed Loons. Blood Hg concentrations reflect dietary uptake of methylmercury (MeHg) from breeding areas and are generally considered near background levels if less than 1.0 µg/g wet weight (ww). Feather (growrn at wintering sites) and egg Hg concentrations can represent a mix of breeding and wintering dietary...

Target-site resistance to pyrethroid insecticides in German populations of the cabbage stem flea beetle, Psylliodes chrysocephala L. (Coleoptera: Chrysomelidae)

Cabbage stem flea beetle, Psylliodes chrysocephala L. (Coleoptera: Chrysomelidae) is a major pest of winter oilseed rape in several European countries particularly attacking young emerging plants in autumn. Over the last several decades, pyrethroid insecticides have been foliarly applied to control flea beetle outbreaks. Recent control failures in northern Germany suggested pyrethroid resistance development in cabbage stem flea beetles, which were confirmed by resistance monitoring bioassays using lambda-cyhalothrin in an adult vial test. The purpose of this study was to investigate the presence of polymorphisms in the para-type voltage-gated sodium channel gene of P. chrysocephala known to be involved in knock-down resistance (kdr). By using a degenerate primer approach we PCR amplified part of the para-type sodium channel gene and identified in resistant flea beetles a single nucleotide polymorphism resulting in an L1014F (kdr) mutation within domain IIS6 of the channel protein, known as one of the chief pyrethroid target-site resistance mechanisms in several other pest insects. Twenty populations including four archived museum samples collected between 1945 and 1958 were analyzed using a newly developed pyrosequencing diagnostic assay. The assay revealed a kdr allele frequency of 90–100% in those flea beetle populations expressing high-level cross-resistance in discriminating dose bioassays against different pyrethroids such as lambda-cyhalothrin, tau-fluvalinate, etofenprox and bifenthrin. The presence of target-site resistance to pyrethroids in cabbage stem flea beetle is extremely worrying considering the lack of effective alternative modes of action to control this pest in Germany and other European countries, and is likely to result in major control problems once it expands to other geographies. The striking fact that cabbage stem flea beetle is next to pollen beetle, Meligethes aeneus the second coleopteran pest in European winter oilseed rape resisting pyrethroid treatments by expressing a target-site mutation, underpins the importance of diversity in available chemistry for resistance management tactics based on mode of action rotation in order to guarantee sustainable winter oilseed rape cultivation in Europe.

Location‐only and use‐availability data: analysis methods converge

Location‐only and use‐availability data: analysis methods converge

Gestión estratégica de los públicos en museos. De la identificación a la comunicación

The current social and cultural environment requires museums to adopt new models of management that include the need to communicate effectively with diverse publics considered important for the development of their activity. The aim of this paper is assess the coherence between the importance assigned to strategic publics and the way museums communicate with them. The study was done on a wide sample (111 entities) of museums in Catalonia. The results indicate consistency with only a few groups, suggesting that museums are still in an early stage of adopting any new models, but a trend towards broadening the scope to include groups of interest other than museum visitors.

Northern range expansion of European populations of the wasp spider Argiope bruennichi is associated with global warming–correlated genetic admixture and population‐specific temperature adaptations

Poleward range expansions are observed for an increasing number of species, which may be an effect of global warming during the past decades. However, it is still not clear in how far these expansions reflect simple geographical shifts of species ranges, or whether new genetic adaptations play a role as well. Here, we analyse the expansion of the wasp spider Argiope bruennichi into Northern Europe during the last century. We have used a range-wide sampling of contemporary populations and historical specimens from museums to trace the phylogeography and genetic changes associated with the range shift. Based on the analysis of mitochondrial, microsatellite and SNP markers, we observe a higher level of genetic diversity in the expanding populations, apparently due to admixture of formerly isolated lineages. Using reciprocal transplant experiments for testing overwintering tolerance, as well as temperature preference and tolerance tests in the laboratory, we find that the invading spiders have possibly shifted their temperature niche. This may be a key adaptation for survival in Northern latitudes. The museum samples allow a reconstruction of the invasion's genetic history. A first, small-scale range shift started around 1930, in parallel with the onset of global warming. A more massive invasion of Northern Europe associated with genetic admixture and morphological changes occurred in later decades. We suggest that the latter range expansion into far Northern latitudes may be a consequence of the admixture that provided the genetic material for adaptations to new environmental regimes. Hence, global warming could have facilitated the initial admixture of populations and this resulted in genetic lineages with new habitat preferences.

Biological variation in a large sample of mouse lemurs from Amboasary, Madagascar: Implications for interpreting variation in primate biology and paleobiology

A thorough knowledge of biological variation in extant primates is imperative for interpreting variation, and for delineating species in primate biology and paleobiology. This is especially the case given the recent, rapid taxonomic expansion in many primate groups, notably among small-bodied nocturnal forms. Here we present data on dental, cranial, and pelage variation in a single-locality museum sample of mouse lemurs from Amboasary, Madagascar. To interpret these data, we include comparative information from other museum samples, and from a newly collected mouse lemur skeletal sample from the Beza Mahafaly Special Reserve (BMSR), Madagascar. We scored forty dental traits (n = 126) and three pelage variants (n = 19), and collected 21 cranial/dental measures. Most dental traits exhibit variable frequencies, with some only rarely present. Individual dental variants include misshapen and supernumerary teeth. All Amboasary pelage specimens display a “reversed V” on the cap, and a distinct dorsal median stripe on the back. All but two displayed the dominant gray–brown pelage coloration typical of Microcebus griseorufus. Cranial and dental metric variability are each quite low, and craniometric variation does not illustrate heteroscedasticity. To assess whether this sample represents a single species, we compared dental and pelage variation to a documented, single-species M. griseorufus sample from BMSR. As at Amboasary, BMSR mouse lemurs display limited odontometric variation and wide variation in non-metric dental traits. In contrast, BMSR mouse lemurs display diverse pelage, despite reported genetic homogeneity. Ranges of dental and pelage variation at BMSR and Amboasary overlap. Thus, we conclude that the Amboasary mouse lemurs represent a single species – most likely (in the absence of genetic data to the contrary) M. griseorufus, and we reject their previous allocation to Microcebus murinus. Patterns of variation in the Amboasary sample provide a comparative template for recognizing the degree of variation manifested in a single primate population, and by implication, they provide minimum values for this species' intraspecific variation. Finally, discordance between different biological systems in our mouse lemur samples illustrates the need to examine multiple systems when conducting taxonomic analyses among living or fossil primates.

Palaeogenetics of western French sturgeons spotlights the relationships between Acipenser sturio and Acipenser oxyrinchus

AbstractAimThe Atlantic sturgeon, Acipenser oxyrinchus, was long considered an American species, but recent discoveries based on analyses of archaeological remains proved its presence in the Baltic Sea and in France. This came as a surprise, as the European sturgeon, Acipenser sturio, was thought to be the only sturgeon species present on the European Atlantic coast. It was hypothesized that migrants from North America founded the Baltic population of Atlantic sturgeons around 1200 years ago.LocationThe sampling is composed of five sturgeon archaeological remains (5000–1800 yr bp) and 21 naturalized or ethanol‐preserved museum specimens from the 19th and 20th centuries, originating from the French Atlantic coast.MethodsAnalyses of ancient DNA were performed following the strict criteria of the field to avoid contamination and to ensure sequence authentication. A 210‐bp fragment of the control region (CR) was sequenced and three microsatellite loci were sized and sequenced.ResultsOut of a total of 26 samples, three archaeological remains and six museum specimens produced A. oxyrinchus mitochondrial or nuclear sequences; two of these museum samples showed signs of hybridization between A. sturio and A. oxyrinchus. All the other samples yielded only A. sturio DNA sequences, and a new CR haplotype was described in this species.Main conclusionsMolecular evidence of sympatry and natural hybridization between A. sturio and A. oxyrinchus on the French Atlantic coast – specifically the hybrid evidence of two museum specimens collected from the Seine River in 1823 and 1858 – challenge our understanding of the species' past relationships. In light of these findings, new hypotheses are presented to explain the history and geographical range of A. oxyrinchus in Europe.

Next-Generation Sequencing for Rodent Barcoding: Species Identification from Fresh, Degraded and Environmental Samples

Rodentia is the most diverse order among mammals, with more than 2,000 species currently described. Most of the time, species assignation is so difficult based on morphological data solely that identifying rodents at the specific level corresponds to a real challenge. In this study, we compared the applicability of 100 bp mini-barcodes from cytochrome b and cytochrome c oxidase 1 genes to enable rodent species identification. Based on GenBank sequence datasets of 115 rodent species, a 136 bp fragment of cytochrome b was selected as the most discriminatory mini-barcode, and rodent universal primers surrounding this fragment were designed. The efficacy of this new molecular tool was assessed on 946 samples including rodent tissues, feces, museum samples and feces/pellets from predators known to ingest rodents. Utilizing next-generation sequencing technologies able to sequence mixes of DNA, 1,140 amplicons were tagged, multiplexed and sequenced together in one single 454 GS-FLX run. Our method was initially validated on a reference sample set including 265 clearly identified rodent tissues, corresponding to 103 different species. Following validation, 85.6% of 555 rodent samples from Europe, Asia and Africa whose species identity was unknown were able to be identified using the BLASTN program and GenBank reference sequences. In addition, our method proved effective even on degraded rodent DNA samples: 91.8% and 75.9% of samples from feces and museum specimens respectively were correctly identified. Finally, we succeeded in determining the diet of 66.7% of the investigated carnivores from their feces and 81.8% of owls from their pellets. Non-rodent species were also identified, suggesting that our method is sensitive enough to investigate complete predator diets. This study demonstrates how this molecular identification method combined with high-throughput sequencing can open new realms of possibilities in achieving fast, accurate and inexpensive species identification.

Assessing the genetic impact of massive restocking on wild mallard

AbstractCaptive‐bred mallards Anas platyrhynchos have been released for hunting purposes at a very large scale in Europe since the mid‐1970s. In spite of a potential genetic impact, the actual contribution of restocked mallards to the genome of the target population has received little attention. The genetic structure of modern wild mallards in the Camargue, Southern France, was assessed from two samples: one originating from shot birds in hunting bags and one from presumed wild ducks captured alive in a hunting‐free reserve. Reference samples originated from five mallard farms, as well as from museum samples collected before the mid‐1970s (i.e. before massive mallard releases started). Our results revealed that the genetic signature of wild wintering mallards has not changed significantly because museum and presumed wild samples from the Camargue hunting‐free nature reserve were genetically similar, and clearly differentiated from the farm mallards. This suggests that mallard releases in the Camargue or elsewhere in France, although massive, have not actually translated into complete admixture of wild and captive genomes, most likely due to low survival of released birds once in the wild. Nevertheless, although genetic introgression of the wild population by captive‐bred was contained, we found significant rates of hybridization between wild and captive‐bred mallards in modern samples. This result suggests that long‐term releases of captive‐bred mallards, if carried on at such large scale, could compromise irreversibly the genetic structure and composition of European mallards. This work contributes to fill in the gap on the monitoring of the genetic consequences of large‐scale game releases for exploitation.

Microsatellite analysis in museum samples reveals inbreeding before the regression of Bombus veteranus

The worldwide decline of pollinators is an emerging threat and is a matter both for ecological and economic concerns. Population genetics can be used to correlate bumblebee decline with genetic parameters. In order to do so, historical data are needed. We used eight microsatellite loci to genotype pinned museum specimens of the declining bumblebee Bombus veteranus. Bumblebee samples were collected spanning a period of three decades (1895–1923). We detected low genetic diversity and inbreeding in the samples collected during the respective time periods. Inbreeding was also confirmed by the occurrence of sterile diploid males. Based on the data obtained, we speculate that low genetic diversity and inbreeding did not directly result in the collapse of B. veteranus in Belgium. However, inbreeding might still play an indirect role in the decline of bumblebee populations because of the appearance of diploid males and because a low H E might reduce the capacity to react to the drivers of bumblebee decline.

Historically low mitochondrial DNA diversity in koalas (Phascolarctos cinereus)

BackgroundThe koala (Phascolarctos cinereus) is an arboreal marsupial that was historically widespread across eastern Australia until the end of the 19th century when it suffered a steep population decline. Hunting for the fur trade, habitat conversion, and disease contributed to a precipitous reduction in koala population size during the late 1800s and early 1900s. To examine the effects of these reductions in population size on koala genetic diversity, we sequenced part of the hypervariable region of mitochondrial DNA (mtDNA) in koala museum specimens collected in the 19th and 20th centuries, hypothesizing that the historical samples would exhibit greater genetic diversity.ResultsThe mtDNA haplotypes present in historical museum samples were identical to haplotypes found in modern koala populations, and no novel haplotypes were detected. Rarefaction analyses suggested that the mtDNA genetic diversity present in the museum samples was similar to that of modern koalas.ConclusionsLow mtDNA diversity may have been present in koala populations prior to recent population declines. When considering management strategies, low genetic diversity of the mtDNA hypervariable region may not indicate recent inbreeding or founder events but may reflect an older historical pattern for koalas.

Unraveling natural versus anthropogenic effects on genetic diversity within the southeastern beach mouse (Peromyscus polionotus niveiventris)

Anthropogenic habitat loss is among the greatest threats to biodiversity. Populations undergoing fragmentation and loss of habitat are also threatened by erosion of genetic diversity. However, contemporary genetic diversity may be the legacy of natural processes acting prior to anthropogenic influences. Measurements of genetic diversity from contemporary and historical samples can evaluate the relative impact of natural and anthropogenic effects on its status. We investigated the genetic diversity of a threatened subspecies occupying Atlantic Coast barrier islands of Florida, Peromyscus polionotus niveiventris (southeastern beach mouse). To test for recent loss of genetic diversity, we compared cyt b data from museum samples (historical—prior to human impact) with contemporary samples throughout their range. Ten microsatellite loci were genotyped for samples from the contemporary range, to determine current population interconnectedness and structure. The results using cyt b data revealed no statistically significant loss of genetic diversity between historical and contemporary populations of P. p. niveiventris. Both nuclear and mitochondrial data support our conclusion that the observed capture and conservation of historical genetic diversity is explained by the large federally protected region of continuous habitat that remains with minimal human impact. Whereas, the two disjunct populations isolated by anthropogenic habitat destruction, exhibit significant losses of genetic diversity. Collectively, these findings offer a sound basis from which to formulate a conservation strategy to maintain the genetic diversity of P. p. niveiventris. Furthermore, our study underscores the importance of large expanses of continuous habitat within the geographic range of species to facilitate the maintenance of genetic integrity.

Historical and modern neutral genetic variability in Mednyi Arctic foxes passed through a severe bottleneck

AbstractSmall isolated populations often show lower genetic variability. Demographic bottlenecks lead to loss of genetic variation too. Arctic foxes (Vulpes lagopus) have been isolated since the Pleistocene on Mednyi and Bering Islands (Commander Islands). In 1970–1980, the Mednyi population passed through a severe bottleneck due to a mange outbreak. Previous studies showed lack of genetic diversity in the contemporary Mednyi population that could be due to the long history of isolation and/or the recent bottleneck. To test both factors, we analyzed the mtDNA D‐loop fragment and five microsatellites in pre‐bottleneck Mednyi museum samples. Also, contemporary Mednyi, Bering and mainland Alaskan Arctic foxes were analyzed. Registered genetic variability in historical Mednyi was higher than in contemporary Mednyi Arctic foxes, but lower than in contemporary the Bering population. Our data confirms that the bottleneck reduced an already depleted polymorphism in Mednyi Arctic foxes. Lack of genetic variability could be a reason why the Mednyi population did not recover following the outbreak of mange.

Genetic differentiation of the African dwarf crocodile Osteolaemus tetraspis Cope, 1861 (Crocodylia: Crocodylidae) and consequences for European zoos

The endangered African dwarf crocodile Osteolaemus tetraspis is distributed in Central and Western Africa. Conventionally, two subspecies were distinguished: Osteolaemus tetraspis tetraspis and Osteolaemus tetraspis osborni. The taxonomic significance of diagnostic morphological characters is still being discussed and the existence of additional species in the Osteolaemus group remains unclear. Recent molecular studies suggest the existence of three allopatric species in the genus Osteolaemus. These results supported a division of the dwarf crocodile into a Congo Basin form (O. osborni), an Ogooue Basin form (O. tetraspis), and a third separate evolutionary lineage from Western Africa. Several European zoos host African dwarf crocodiles. For reasons of conservation and possible reintroduction, it is important to clarify provenance of these zoo animals. Therefore, we conducted molecular and phylogenetic analyses of three mitochondrial and two nuclear gene sequences with all available samples from European zoos and museums. We also estimated the origin of the zoo animals by comparing sequences of wild animals and museum samples of known provenance. Our study strongly supports three distinct lineages of Osteolaemus as recently postulated, but also reveals a fourth evolutionary lineage. We demonstrate that, of the European zoo animals sampled, only one dwarf crocodile corresponds to the Congo Basin form (O. osborni) whereas the majority of individuals correspond to the three other forms. Four zoo animals belong to the new fourth group; but their provenance is still unresolved. The origin of these animals is probably located in an African region from which no wild animal samples are currently available. Further investigations and sampling of other regions should be completed to clarify the identity of this fourth lineage. We found potential hybrids from European zoological gardens using nuclear DNA sequences. The European Studbook will use these results for further breeding programmes to keep genetically suitable ex-situ populations as reassurance colonies for prospective reintroduction into African countries.

The Development of a Genome Wide SNP Set for the Barnacle Goose Branta leucopsis

Migratory birds are of particular interest for population genetics because of the high connectivity between habitats and populations. A high degree of connectivity requires using many genetic markers to achieve the required statistical power, and a genome wide SNP set can fit this purpose. Here we present the development of a genome wide SNP set for the Barnacle Goose Branta leucopsis, a model species for the study of bird migration. We used the genome of a different waterfowl species, Mallard Anas platyrhynchos, as a reference to align Barnacle Goose second generation sequence reads from an RRL library and detected 2188 SNPs genome wide. Furthermore, we used chimeric flanking sequences, merged from both Mallard and Barnacle Goose DNA sequence information, to create primers for validation by genotyping. Validation with a 384 SNP genotyping set resulted in 374 (97%) successfully typed SNPs in the assay, of which 358 (96%) were polymorphic. Additionally, we validated our SNPs on relatively old (30 years) museum samples, which resulted in a success rate of at least 80%. This shows that museum samples could be used in standard SNP genotyping assays. Our study also shows that the genome of a related species can be used as reference to detect genome wide SNPs in birds, because genomes of birds are highly conserved. This is illustrated by the use of chimeric flanking sequences, which showed that the incorporation of flanking nucleotides from Mallard into Barnacle Goose sequences lead to equal genotyping performance when compared to flanking sequences solely composed of Barnacle Goose sequence.

Barcoding Sponges: An Overview Based on Comprehensive Sampling

BackgroundPhylum Porifera includes ∼8,500 valid species distributed world-wide in aquatic ecosystems ranging from ephemeral fresh-water bodies to coastal environments and the deep-sea. The taxonomy and systematics of sponges is complicated, and morphological identification can be both time consuming and erroneous due to phenotypic convergence and secondary losses, etc. DNA barcoding can provide sponge biologists with a simple and rapid method for the identification of samples of unknown taxonomic membership. The Sponge Barcoding Project (www.spongebarcoding.org), the first initiative to barcode a non-bilaterian metazoan phylum, aims to provide a comprehensive DNA barcode database for Phylum Porifera.Methodology/Principal Findings∼7,400 sponge specimens have been extracted, and amplification of the standard COI barcoding fragment has been attempted for approximately 3,300 museum samples with ∼25% mean amplification success. Based on this comprehensive sampling, we present the first report on the workflow and progress of the sponge barcoding project, and discuss some common pitfalls inherent to the barcoding of sponges.ConclusionA DNA-barcoding workflow capable of processing potentially large sponge collections has been developed and is routinely used for the Sponge Barcoding Project with success. Sponge specific problems such as the frequent co-amplification of non-target organisms have been detected and potential solutions are currently under development. The initial success of this innovative project have already demonstrated considerable refinement of sponge systematics, evaluating morphometric character importance, geographic phenotypic variability, and the utility of the standard barcoding fragment for Porifera (despite its conserved evolution within this basal metazoan phylum).

Characterization of nine microsatellite loci in the European polecat Mustela putorius

We developed a set of nine polymorphic microsatellite markers from a genomic library enriched for dinucleotide repeats in the European polecat Mustela putorius. Microsatellite loci amplification was tested on fresh tissues and museum samples collected over the last 40 years in central and northern Italy. Number of alleles per locus ranged from 3 to 7. Mean observed and expected heterozygosity were 0.48 and 0.61, respectively. This novel set of species-specific microsatellite loci will be particularly useful to assess fine patterns of genetic structure and degree of isolation of European polecat populations.

Genetic indications of translocated and stocked grey partridges (Perdix perdix): does the indigenous Danish grey partridge still exist?

Non-local population stocking can have adverse genetic effects through loss of genetic diversity and introgressive hybridisation in wild populations exploited by man. The grey partridge (Perdix perdix) has been an important European game species for centuries, widely subject to translocation and stocking. After ca 80 years releasing reared grey partridges into Danish wild partridge areas, this study investigated whether an indigenous Danish grey partridge still existed. We predicted that (i) an indigenous Danish partridge would belong to the western European clade (W1) and (ii) would be more closely related to the historical, indigenous grey partridges than to farm bred partridges. These predictions were tested analysing the variation in the mitochondrial control region (CR1) and microsatellite markers in museum samples representing the ancestral indigenous Danish grey partridge, contemporary (recent) wild grey partridges and farmed grey partridges from the five largest farms in Denmark. Phylogeography- and population structure analyses showed traces of the indigenous Danish grey partridges amongst recent wild partridges in certain areas and significant genetic differences between reared, farmed partridges and historical- and recent partridges. The results also showed that the indigenous Danish grey partridges belonged to the western European clade (W1 haplotype). A foreign stocking effect was detected on the remote island of Bornholm, where the current population originated from introduced Danish and Bohemian grey partridges. The loss of haplotype diversity over time in certain geographical areas probably results from serious declines in wild Danish grey partridge numbers in recent decades. This combined with the 2 observation that hybridisation between released stocked and wild partridges can occur may complicate recovery of partridge populations.

Hibernation does not reduce cortical bone density, area or second moments of inertia in woodchucks (Marmota monax)

Long periods of inactivity in most mammals result in bone loss that may not be completely recoverable during an individual's lifetime regardless of future activity. Prolonged inactivity is normal during hibernation, but it remains uncertain whether hibernating mammals suffer decreased bone properties after hibernation that affects survival. We test the hypothesis that relative cortical area (C(A) ), apparent density, bone area fraction (B.Ar/T.Ar), and moments of inertia do not differ between museum samples of woodchucks (Marmota monax) collected before and after hibernation. We used peripheral quantitative computed tomography to examine bone geometry in the femur, tibia, humerus and mandible. We see little evidence for changes in bone measures with hibernation supporting our hypothesis. In fact, when including subadults to increase sample sizes and controlling age statistically, we observed a trend toward increased bone properties following hibernation. Diaphyses were significantly denser in the humerus, femur, and tibia after hibernation, and relative mandibular cortical area was significantly larger. Similarly, relative mechanical indices were significantly larger in the mandible after hibernation. Although tests of individual measures in many cases were not significantly different prehibernation versus posthibernation, the overall pattern of average increase posthibernation was significant for relative C(A) and densities as well as relative diaphyseal mechanical indices when examining outcomes collectively. The exception to this pattern was a reduction in metaphyseal trabecular bone following hibernation. Individually, only humeral B.Ar/T.Ar was significantly reduced, but the average reduction in trabecular measures post-hibernation was significant when examined collectively. Because the sample included subadults, we suggest that much of the increased bone relates to their continued growth during hibernation. Our results indicate that woodchucks are more similar to large hibernators that maintain skeletal integrity compared to smaller-bodied hibernators that may lose bone. This result suggests a potential size-related trend in bone response to hibernation across mammals.