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Data from: Survey sequencing reveals elevated DNA transposon activity, novel elements, and variation in repetitive landscapes among vesper bats
负责人:
关键词:
Corynorhinus rafinesquii;Myotis austroriparius;Nycticeius humeralis;Perimyotis subflavus;Lasiurus borealis;transposable element;Survey sequence;Chiroptera
DOI:
doi:10.5061/dryad.83164r7v
摘要:
TEs were obtained from the little brown bat, Myotis lucifugus and are reflected by higher genome content (~5%). To aid in determining taxonomic limits
Data from: Conservation implications of ameliorating survival of little brown bats with White-Nose Syndrome
负责人:
关键词:
Barker model;wildlife disease;Myotis lucifugus;population viability analysis;hibernacula;little brown bat;mark-recapture;WNS;Geomyces destructans;Pseudogymnoascus destructans;vital rate sensitivity;white-nose syndrome
DOI:
doi:10.5061/dryad.85709
摘要:
by this disease. Using mark–recapture data on infected little brown bats (Myotis lucifugus), we estimated the first apparent annual survival rates for four yea
Data from: Population genetic structure of a common host predicts the spread of white-nose syndrome, an emerging infectious disease in bats
负责人:
关键词:
Host Parasite Interactions Landscape Genetics Mammals Phylogeography Population Genetics - Empirical
DOI:
doi:10.5061/dryad.v1v13
摘要:
ons. We tested for a relationship between the population genetic structure of the most common host, the little brown myotis (Myotis lucifugus), and the geographic
Data from: Multi-scale model of regional population decline in little brown bats due to white-nose syndrome
负责人:
关键词:
white-nose syndrome;Pseudogymnoascus destrucans;Myotis lucifugus;plausible parameter sets;little brown bat;metapopulation dynamics;Disease model
DOI:
doi:10.5061/dryad.nr75483
摘要:
and to identify gaps in knowledge about key processes, and could be expanded to include additional mechanisms or bat species as research on this detrimental fungus
Data from: Here and there, but not everywhere: repeated loss of uncoupling protein 1 in amniotes
负责人:
关键词:
Gavia stellata;Canis familiaris;Haliaeetus albicilla;Balaenoptera acutorostrata;Anolis carolinensis;Picoides pubescens;Cuculus canorus;Pteropus vampyrus;Merops nubicus;Cavia porcellus;Struthio camelus australis;Pseudopodoces humilis;Aquila chrysaetos canadensis;Meleagris gallopavo;Serinus canaria;Procavia capensis;Sarcophilus harrisii;Tupaia belangeri;Zonotrichia albicollis;Buceros rhinoceros silvestris;Homo Sapiens;Dipodomys ordii;Papio anubis;Candoia aspera;Melopsittacus undulatus;Pan troglogdytes;Myotis lucifugus;Thamnophis couchii;Corvus cornix cornix;Sus scrofa;Sceloporus undulatus;Charadrius vociferus;Rattus norvegicus;Crocodylus porosus?;Alligator sinensis;Tauraco erythrolophus;Erinaceus europaeus;Microcebus murinus;Nipponia nippon;Xenopeltis unicolor;Ophiophagus hannah;Choloepus hoffmanni;Myotis brandtii;Dasypus novemcinctus;Tinamus guttatus;Pygoscelis adeliae;Orcinus orca;Tursiops truncatus;Phaethon lepturus;Phalacrocorax carbo;Falco cherrug;Alligator mississippiensis;Microtus ochrogaster;Tyto alba;heterocephalus glaber;Aptenodytes forsteri;Apaloderma vittatum;Macropus eugenii;Chlorocebus sabaeus;Cariama cristata;Egretta garzetta;Pterocles gutturalis;Agkistrodon piscivorus;Macaca mulatta;Felis catus;Physeter macrocephalus;Calypte anna;Gavialis gangeticus;Vicugna pacos;Elgaria multicarinata;Manacus vitellinus;Chaetura pelagica;Gallus gallus;Otolemur garnettii;Pelecanus crispus;turtle;Anolis sagrei;Bos taurus;Balearica regulorum gibbericeps;Chelonia mydas;thermogenesis;Sorex araneus;Ovis aries;Nestor notabilis;Mesitornis unicolor;Opisthocomus hoazin;Python molurus bivittatus;cetacean;Equus caballus;Chrysemys picta;Ficedula albicollis;Mus musculus;Ochotona princeps;Pogona vitticeps;Callithrix jacchus;Colius striatus;Leptosomus discolor;UCP1;Snake;Lamprophis fuliginosus;Anser cygnoides domesticus;Terrapene ornata;Gorilla gorilla;Oryctolagus cuniculus;Fulmarus glacialis;Corvus brachyrhynchos;Sternotherus odoratus;Taeniopygia guttata;Eublepharis macularius;Pongo abelii;Caprimulgus carolinensis;lizard;Monodelphis domestica;Haliaeetus leucocephalus;Mustela putorius;Pelodiscus sinensis;Pelusios castaneus;Chlamydotis macqueenii;Eurypyga helias;Ornithorhynchus anatinus;Columba livia;Loxodonta africana;Echinops telfairi;Falco peregrinus;Nomascus leucogenys;Geospiza fortis;Scincella lateralis;Thamnophis elegans;Tarsius syrichta;Ictidomys tridecemlineatus;Anas platyrhynchos;Ailuropoda melanoleuca;Cheyldra serpentina
DOI:
doi:10.5061/dryad.934fg
摘要:
ve nonshivering thermogenesis (NST). Although ucp1 arose early in the vertebrate lineage, the loss of ucp1 was previously documented in several reptile species (including birds
Data from: Higher fat stores contribute to persistence of little brown bat populations with white-nose syndrome
负责人:
Cheng, Tina
关键词:
Emerging infectious disease tolerance resistance plasticity evolution trait change
DOI:
doi:10.5061/dryad.sh487nh
摘要:
depletion and starvation. However, some populations of Myotis lucifugus now persist with WNS by unknown mechanisms. 2. We examined whether persistence
Data from: Determining the null model for detecting adaptive convergence from genomic data: a case study using echolocating mammals
负责人:
关键词:
Echolocation;Pteropus vampyrus;convergence;Myotis lucifugus;Adaptation;Tursiops truncatus
DOI:
doi:10.5061/dryad.16qc5
摘要:
-specific likelihood support (SSLS) generated using simulated topologies, they concluded that there was evidence for genome-wide adaptive convergence bet
Data from: Divergent evolutionary rates in vertebrate and mammalian specific Conserved Non-coding Elements (CNEs) in echolocating mammals
负责人:
关键词:
ear development;bats;Pteropus vampyrus;Mammalia;conserved non-coding elements;Myotis lucifugus;Rhinolophus ferrumequinum;Megaderma lyra;Cetacea;Eidolon helvum;Pteronotus parnellii;Chiroptera
DOI:
doi:10.5061/dryad.50kd5
摘要:
spatial association with key developmental genes – such as those regulating the development of the sensory systems – suggests crucial roles in regulati

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