Mitogenome of a Cryptic Species Within Uropsilus and Divergence Time Estimation
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Cryptic Phylogeographic History Sheds Light on the Generation of Species Diversity in Sky-Island Mountains
bioRxiv preprint doi: https://doi.org/10.1101/199786; this version posted October 7, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Cryptic phylogeographic history sheds light on the generation of species diversity in sky-island mountains Kai He1, 2, 3, #, Tao Wan 1, 4, Klaus-Peter Koepfli 5, 6, Wei Jin7, Shao-Ying Liu7, Xue-Long Jiang1, # 1 State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China 2 Department of Biological Sciences, University of Manitoba, Winnipeg, MN R3T R3V, Canada 3 The Kyoto University Museum, Kyoto University, Kyoto 606-8501, Japan. 4 Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming, Yunnan 650223, China 5 Smithsonian Conservation Biology Institute, National Zoological Park, DC 20008, USA 6 Theodosius Dobzhansky Center for Genome Bioinformatics, Saint Petersburg State University, St. Petersburg 199034, RUSSIA 7 Sichuan Academy of Forest, Chengdu 610081, Sichuan, China Keywords: allopatry, Approximate Bayesian Computation, cryptic corridor, interglacial refugia, niche modeling, species delimitation Running title: Cryptic sky-island phylogeography # Correspondence: Kai He and Xue-Long Jiang, Fax: 86 871 6512 5226; E-mails: [email protected], [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/199786; this version posted October 7, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
Uropsilus, Talpidae): Implications for Taxonomy and Conservation Tao Wan1,2†, Kai He1,3† and Xue-Long Jiang1*
Wan et al. BMC Evolutionary Biology 2013, 13:232 http://www.biomedcentral.com/1471-2148/13/232 RESEARCH ARTICLE Open Access Multilocus phylogeny and cryptic diversity in Asian shrew-like moles (Uropsilus, Talpidae): implications for taxonomy and conservation Tao Wan1,2†, Kai He1,3† and Xue-Long Jiang1* Abstract Background: The genus Uropsilus comprises a group of terrestrial, montane mammals endemic to the Hengduan and adjacent mountains. These animals are the most primitive living talpids. The taxonomy has been primarily based on cursory morphological comparisons and the evolutionary affinities are little known. To provide insight into the systematics of this group, we estimated the first multi-locus phylogeny and conducted species delimitation, including taxon sampling throughout their distribution range. Results: We obtained two mitochondrial genes (~1, 985 bp) and eight nuclear genes (~4, 345 bp) from 56 specimens. Ten distinct evolutionary lineages were recovered from the three recognized species, eight of which were recognized as species/putative species. Five of these putative species were found to be masquerading as the gracile shrew mole. The divergence time estimation results indicated that climate change since the last Miocene and the uplift of the Himalayas may have resulted in the diversification and speciation of Uropsilus. Conclusions: The cryptic diversity found in this study indicated that the number of species is strongly underestimated under the current taxonomy. Two synonyms of gracilis (atronates and nivatus) should be given full species status, and the taxonomic status of another three potential species should be evaluated using extensive taxon sampling, comprehensive morphological, and morphometric approaches. Consequently, the conservation status of Uropsilus spp. -
Zootaxa, a New Species of Crocidura (Soricomorpha: Soricidae) From
Zootaxa 2345: 60–68 (2010) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2010 · Magnolia Press ISSN 1175-5334 (online edition) A new species of Crocidura (Soricomorpha: Soricidae) from southern Vietnam and north-eastern Cambodia PAULINA D. JENKINS1, ALEXEI V. ABRAMOV2,4, VIATCHESLAV V. ROZHNOV3,4 & ANNETTE OLSSON5 1The Natural History Museum, Cromwell Road, London SW7 5BD, UK. E-mail: [email protected] 2Zoological Institute, Russian Academy of Sciences, Universitetskaya nab., 1, Saint-Petersburg, 199034, Russia. E-mail: [email protected] 3A.N. Severtsov Institute of Ecology and Evolution, Russian Academy of Sciences, Leninskii pr., 33, Moscow, 119071, Russia. E-mail: [email protected] 4Joint Vietnam-Russian Tropical Research and Technological Centre, Nguyen Van Huyen, Nghia Do, Cau Giay, Hanoi, Vietnam. E-mail: [email protected] 5Conservation International – Cambodia Programme, P.O. Box 1356, Phnom Penh, Cambodia. E-mail: [email protected] Abstract Knowledge of the Soricidae occurring in Vietnam has recently expanded with the discovery of several species previously unknown to science. Here we describe a new species of white-toothed shrew belonging to the genus Crocidura from lowland areas in southern Vietnam and from a river valley in north-eastern Cambodia. This small to medium sized species is diagnosed on the basis of external features, cranial proportions and morphology of the last upper and lower molars. Comparisons are made with other species of Crocidura known to occur in Vietnam and the biogeography of the regions where the new species has been found, is briefly discussed. Key words: white-toothed shrew, Vietnam, Cambodia Introduction Knowledge of the soricid fauna of South-East Asia and particularly that of Vietnam is still poorly understood, while that of Cambodia is virtually unknown (Jenkins, 1982; Heaney & Timm, 1983; Jenkins & Smith, 1995; Motokawa et al., 2005; Jenkins et al., 2009). -
When Beremendiin Shrews Disappeared in East Asia, Or How We Can Estimate Fossil Redeposition
Historical Biology An International Journal of Paleobiology ISSN: (Print) (Online) Journal homepage: https://www.tandfonline.com/loi/ghbi20 When beremendiin shrews disappeared in East Asia, or how we can estimate fossil redeposition Leonid L. Voyta , Valeriya E. Omelko , Mikhail P. Tiunov & Maria A. Vinokurova To cite this article: Leonid L. Voyta , Valeriya E. Omelko , Mikhail P. Tiunov & Maria A. Vinokurova (2020): When beremendiin shrews disappeared in East Asia, or how we can estimate fossil redeposition, Historical Biology, DOI: 10.1080/08912963.2020.1822354 To link to this article: https://doi.org/10.1080/08912963.2020.1822354 Published online: 22 Sep 2020. Submit your article to this journal View related articles View Crossmark data Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ghbi20 HISTORICAL BIOLOGY https://doi.org/10.1080/08912963.2020.1822354 ARTICLE When beremendiin shrews disappeared in East Asia, or how we can estimate fossil redeposition Leonid L. Voyta a, Valeriya E. Omelko b, Mikhail P. Tiunovb and Maria A. Vinokurova b aLaboratory of Theriology, Zoological Institute, Russian Academy of Sciences, Saint Petersburg, Russia; bFederal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch of Russian Academy of Sciences, Vladivostok, Russia ABSTRACT ARTICLE HISTORY The current paper first time describes a small Beremendia from the late Pleistocene deposits in the Received 24 July 2020 Koridornaya Cave locality (Russian Far East), which associated with the extinct Beremendia minor. The Accepted 8 September 2020 paper is the first attempt to use a comparative analytical method to evaluate a possible case of redeposition KEYWORDS of fossil remains of this shrew. -
Solenodon Genome Reveals Convergent Evolution of Venom in Eulipotyphlan Mammals
Solenodon genome reveals convergent evolution of venom in eulipotyphlan mammals Nicholas R. Casewella,1, Daniel Petrasb,c, Daren C. Cardd,e,f, Vivek Suranseg, Alexis M. Mychajliwh,i,j, David Richardsk,l, Ivan Koludarovm, Laura-Oana Albulescua, Julien Slagboomn, Benjamin-Florian Hempelb, Neville M. Ngumk, Rosalind J. Kennerleyo, Jorge L. Broccap, Gareth Whiteleya, Robert A. Harrisona, Fiona M. S. Boltona, Jordan Debonoq, Freek J. Vonkr, Jessica Alföldis, Jeremy Johnsons, Elinor K. Karlssons,t, Kerstin Lindblad-Tohs,u, Ian R. Mellork, Roderich D. Süssmuthb, Bryan G. Fryq, Sanjaya Kuruppuv,w, Wayne C. Hodgsonv, Jeroen Kooln, Todd A. Castoed, Ian Barnesx, Kartik Sunagarg, Eivind A. B. Undheimy,z,aa, and Samuel T. Turveybb aCentre for Snakebite Research & Interventions, Liverpool School of Tropical Medicine, Pembroke Place, L3 5QA Liverpool, United Kingdom; bInstitut für Chemie, Technische Universität Berlin, 10623 Berlin, Germany; cCollaborative Mass Spectrometry Innovation Center, University of California, San Diego, La Jolla, CA 92093; dDepartment of Biology, University of Texas at Arlington, Arlington, TX 76010; eDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138; fMuseum of Comparative Zoology, Harvard University, Cambridge, MA 02138; gEvolutionary Venomics Lab, Centre for Ecological Sciences, Indian Institute of Science, 560012 Bangalore, India; hDepartment of Biology, Stanford University, Stanford, CA 94305; iDepartment of Rancho La Brea, Natural History Museum of Los Angeles County, Los Angeles, -
Convergent Evolution of Olfactory and Thermoregulatory Capacities in Small Amphibious Mammals
Convergent evolution of olfactory and thermoregulatory capacities in small amphibious mammals Quentin Martineza,1, Julien Clavelb,c, Jacob A. Esselstynd,e, Anang S. Achmadif, Camille Grohég,h, Nelly Piroti,j, and Pierre-Henri Fabrea,k aInstitut des Sciences de l’Évolution de Montpellier (ISEM), CNRS, Institut de recherche pour le développement (IRD), Université de Montpellier (UM), UMR 5554, 34095 Montpellier, France; bDepartment of Life Sciences, The Natural History Museum, SW7 5DB London, United Kingdom; cUniv. Lyon Laboratoire d’Ecologie des Hydrosystèmes Naturels et Anthropisés, UMR CNRS 5023, Université Claude Bernard Lyon 1, École Nationale des Travaux Publics de l’État (ENTPE), F‐69622 Villeurbanne, Cedex, France; dMuseum of Natural Science, Louisiana State University, Baton Rouge, LA 70803; eDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803; fMuseum Zoologicum Bogoriense, Research Center for Biology, Indonesian Institute of Sciences (LIPI), 16911 Cibinong, Indonesia; gDivision of Paleontology, American Museum of Natural History, New York, NY 10024; hLaboratoire Paléontologie Évolution Paléoécosystèmes Paléoprimatologie (PALEVOPRIM, UMR 7262, CNRS-Institut écologie et environnement [INEE]), Université de Poitiers, 86073 Poitiers, Cedex 9, France; iInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM, U1194 UM, Institut du Cancer de Montpellier (ICM), F-34298 Montpellier, Cedex 5, France; jRéseau d’Histologie Expérimentale de Montpellier, UMS3426 CNRS-US009 INSERM-UM, 34298 Montpellier, France; and kMammal Section, Department of Life Sciences, The Natural History Museum, SW7 5DB London, United Kingdom Edited by David B. Wake, University of California, Berkeley, CA, and approved February 28, 2020 (received for review October 11, 2019) Olfaction and thermoregulation are key functions for mammals. The partitioning has been documented in histological, airflow dynamic, former is critical to feeding, mating, and predator avoidance behaviors, and performance test studies (9–13). -
Molecular Phylogenetics of Shrews (Mammalia: Soricidae) Reveal Timing of Transcontinental Colonizations
Molecular Phylogenetics and Evolution 44 (2007) 126–137 www.elsevier.com/locate/ympev Molecular phylogenetics of shrews (Mammalia: Soricidae) reveal timing of transcontinental colonizations Sylvain Dubey a,*, Nicolas Salamin a, Satoshi D. Ohdachi b, Patrick Barrie`re c, Peter Vogel a a Department of Ecology and Evolution, University of Lausanne, CH-1015 Lausanne, Switzerland b Institute of Low Temperature Science, Hokkaido University, Sapporo 060-0819, Japan c Laboratoire Ecobio UMR 6553, CNRS, Universite´ de Rennes 1, Station Biologique, F-35380, Paimpont, France Received 4 July 2006; revised 8 November 2006; accepted 7 December 2006 Available online 19 December 2006 Abstract We sequenced 2167 base pairs (bp) of mitochondrial DNA cytochrome b and 16S, and 1390 bp of nuclear genes BRCA1 and ApoB in shrews taxa (Eulipotyphla, family Soricidae). The aim was to study the relationships at higher taxonomic levels within this family, and in particular the position of difficult clades such as Anourosorex and Myosorex. The data confirmed two monophyletic subfamilies, Soric- inae and Crocidurinae. In the former, the tribes Anourosoricini, Blarinini, Nectogalini, Notiosoricini, and Soricini were supported. The latter was formed by the tribes Myosoricini and Crocidurini. The genus Suncus appeared to be paraphyletic and included Sylvisorex.We further suggest a biogeographical hypothesis, which shows that North America was colonized by three independent lineages of Soricinae during middle Miocene. Our hypothesis is congruent with the first fossil records for these taxa. Using molecular dating, the first exchang- es between Africa and Eurasia occurred during the middle Miocene. The last one took place in the Late Miocene, with the dispersion of the genus Crocidura through the old world. -
Alexis Museum Loan NM
STANFORD UNIVERSITY STANFORD, CALIFORNIA 94305-5020 DEPARTMENT OF BIOLOGY PH. 650.725.2655 371 Serrra Mall FAX 650.723.0589 http://www.stanford.edu/group/hadlylab/ [email protected] 4/26/13 Joseph A. Cook Division of Mammals The Museum of Southwestern Biology at the University of New Mexico Dear Joe: I am writing on behalf of my graduate student, Alexis Mychajliw and her collaborator, Nat Clarke, to request the sampling of museum specimens (tissue, skins, skeletons) for DNA extraction for use in our study on the evolution of venom genes within Eulipotyphlan mammals. Please find included in this request the catalogue numbers of the desired specimens, as well as a summary of the project in which they will be used. We have prioritized the use of frozen or ethanol preserved tissues to avoid the destruction of museum skins, and seek tissue samples from other museums if only skins are available for a species at MSB. The Hadly lab has extensive experience in the non-destructive sampling of specimens for genetic analyses. Thank you for your consideration and assistance with our research. Please contact Alexis ([email protected]) with any questions or concerns regarding our project or sampling protocols, or for any additional information necessary for your decision and the processing of this request. Alexis is a first-year student in my laboratory at Stanford and her project outline is attached. As we are located at Stanford University, we are unable to personally pick up loan materials from the MSB. We request that you ship materials to us in ethanol or buffer. -
Talpid Mole Phylogeny Unites Shrew Moles and Illuminates Overlooked Cryptic Species Diversity Kai He,‡,†,1,2 Akio Shinohara,†,3 Kristofer M
Talpid Mole Phylogeny Unites Shrew Moles and Illuminates Overlooked Cryptic Species Diversity Kai He,‡,†,1,2 Akio Shinohara,†,3 Kristofer M. Helgen,4 Mark S. Springer,5 Xue-Long Jiang,*,1 and Kevin L. Campbell*,2 1State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China 2Department of Biological Sciences, University of Manitoba, Winnipeg, MN , Canada 3Department of Bio-resources, Division of Biotechnology, Frontier Science Research Center, University of Miyazaki, Miyazaki, Japan 4National Museum of Natural History Smithsonian Institution, Washington, DC 5Department of Biology, University of California, Riverside, CA ‡Present address: The Kyoto University Museum, Kyoto University, Kyoto, Japan †These authors contributed equally to this work. *Corresponding authors: E-mails: [email protected]; [email protected] Associate editor: Emma Teeling Abstract The mammalian family Talpidae (moles, shrew moles, desmans) is characterized by diverse ecomorphologies associated with terrestrial, semi-aquatic, semi-fossorial, fossorial, and aquatic-fossorial lifestyles. Prominent specializations involved with these different lifestyles, and the transitions between them, pose outstanding questions regarding the evolutionary history within the family, not only for living but also for fossil taxa. Here, we investigate the phylogenetic relationships, divergence times, and biogeographic history of the family using 19 nuclear and 2 mitochondrial genes (16 kb) from 60% of described species representing all 17 genera. Our phylogenetic analyses help settle classical questions in the evolution of moles, identify an ancient (mid-Miocene) split within the monotypic genus Scaptonyx, and indicate that talpid species richness may be nearly 30% higher than previously recognized. Our results also uniformly support the monophyly of long-tailed moles with the two shrew mole tribes and confirm that the Gansu mole is the sole living Asian member of an otherwise North American radiation. -
2014 Annual Reports of the Trustees, Standing Committees, Affiliates, and Ombudspersons
American Society of Mammalogists Annual Reports of the Trustees, Standing Committees, Affiliates, and Ombudspersons 94th Annual Meeting Renaissance Convention Center Hotel Oklahoma City, Oklahoma 6-10 June 2014 1 Table of Contents I. Secretary-Treasurers Report ....................................................................................................... 3 II. ASM Board of Trustees ............................................................................................................ 10 III. Standing Committees .............................................................................................................. 12 Animal Care and Use Committee .......................................................................... 12 Archives Committee ............................................................................................... 14 Checklist Committee .............................................................................................. 15 Conservation Committee ....................................................................................... 17 Conservation Awards Committee .......................................................................... 18 Coordination Committee ....................................................................................... 19 Development Committee ........................................................................................ 20 Education and Graduate Students Committee ....................................................... 22 Grants-in-Aid Committee -
Surface Foraging in Scapanus Moles
Mammalia 2017; aop Vladimir Dinets* Surface foraging in Scapanus moles DOI 10.1515/mammalia-2016-0091 species that forages underwater, underground and on the Received July 3, 2016; accepted November 29, 2016 surface (Condylura; Nowak 1999, Smith and Xie 2013). Western American moles (Scapanus) are believed Abstract: Some mole genera, including Scapanus of west- to be exclusively underground foragers (Stephens 1906 ern North America, are usually considered to be fully fos- and virtually all subsequent works), although they are sorial. I present data showing that surface foraging is used known to forage under snow in winter in colder parts of by adults of all four Scapanus species, and evidence that their range (Pedersen 1963). Regular occurrence of their such foraging is not a particularly rare behavior. Scapanus remains in owl pellets and among animals killed by moles forage on the surface when leaf litter is wet and domestic cats and dogs (Giger 1965, Maser and Brodie does not produce much noise; they also move slowly, 1966) and by other predators (see Carraway et al. 1993 for remain within a small area, and usually forage in places an overview) is interpreted as evidence of either surface with dense cover. These adaptations decrease the risk of dispersal by juveniles (Giger 1965, Verts and Carraway predation and make surface foraging behavior difficult to 2001) or movement of males seeking females (Naughton detect for human observers. Numerous unpublished and 2012). The former view is supported by the fact that almost a few published observations suggest that many, if not all skulls collected from owl and raptor pellets belong to all, species in other “fully fossorial” mole genera forage juveniles (Pedersen 1963, Giger 1965). -
Myoglobin Primary Structure Reveals Multiple Convergent Transitions To
RESEARCH ARTICLE Myoglobin primary structure reveals multiple convergent transitions to semi- aquatic life in the world’s smallest mammalian divers Kai He1,2,3,4*, Triston G Eastman1, Hannah Czolacz5, Shuhao Li1, Akio Shinohara6, Shin-ichiro Kawada7, Mark S Springer8, Michael Berenbrink5*, Kevin L Campbell1* 1Department of Biological Sciences, University of Manitoba, Winnipeg, Canada; 2Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China; 3State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China; 4Guangdong Provincial Key Laboratory of Single Cell Technology and Application, Southern Medical University, Guangzhou, China; 5Department of Evolution, Ecology and Behaviour, University of Liverpool, Liverpool, United Kingdom; 6Department of Bio-resources, Division of Biotechnology, Frontier Science Research Center, University of Miyazaki, Miyazaki, Japan; 7Department of Zoology, Division of Vertebrates, National Museum of Nature and Science, Tokyo, Japan; 8Department of Evolution, Ecology and Organismal Biology, University of California, Riverside, Riverside, United States *For correspondence: Abstract The speciose mammalian order Eulipotyphla (moles, shrews, hedgehogs, solenodons) [email protected] (KH); combines an unusual diversity of semi-aquatic, semi-fossorial, and fossorial forms that arose from [email protected]. terrestrial forbearers. However, our understanding of