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276 results for “Myotis myotis”

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dryad36/100

Drivers of longitudinal telomere dynamics in the long-lived bat species, Myotis myotis

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publicMar 2020View details →
dryad36/100

Little brown myotis social networks

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publicJan 2022View details →
dryad36/100

Genotyping-by-sequencing Single-nucleotide Polymorphism Dataset for Corynorhinus rafinesquii (CORA) and Myotis austroriparius (MYAU)

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publicAug 2024View details →
dryad36/100

The soundscape of swarming: Proof of concept for a non-invasive acoustic species identification of swarming Myotis bats

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publicOct 2022View details →
edi36/100

Fernow Experimental Forest site, station Fernow Experimental Forest, study of animal abundance of Myotis sodalis in units of number on a yearly timescale

The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Fernow Experimental Forest (FER) contains animal abundance of Myotis sodalis measurements in number units and were aggregated to a yearly timescale.

openOpenJan 2020View details →
zenodo32/100

FIGURE 9 in Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China

FIGURE 9. Skulls of (a) M. soror sp. n. (HNHM 2003.36.20, holotype), (b) Myotis frater from Fujian, China (AMNH 48029, holotype), and (c) M. frater from Taiwan (HNHM 2004.19.3). Scale= 5 mm.

opennotspecifiedDec 2015View details →
zenodo32/100

FIG. 5 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'

FIG. 5. Camera lucida tracings of the skull of M. annatessae sp. nov. (paratype ZMMU S-165043). Scale bar = 5 mm

opennotspecifiedNov 2013View details →
zenodo32/100

FIG. 4 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'

FIG. 4. Neighbour-joining tree of COI sequences of 25 species of Eurasian Myotis included in comparative molecular analysis (see Appendix for list of sequences used). Only bootstrap supports over 70% are shown

opennotspecifiedNov 2013View details →
zenodo32/100

FIG. 2. Bivariate scatterplot for the 1 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'

FIG. 2. Bivariate scatterplot for the 1st and 2nd Principal Components, calculated for 20 cranial and dental measurements of 100 specimens of small Asian mouse-eared bats. For factor loadings and eigenvalues, see Table 1

opennotspecifiedNov 2013View details →
zenodo32/100

FIG. 3 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'

FIG. 3. Camera lucida traces of penial bones (bacula) in five smaller species of the Asiatic Myotis: a, b — M. annatessae sp. nov., Vietnam, ZMMU S-164989 (dorsal, ventral, right lateral views), ZMMU S-165043 (dorsal, ventro-lateral, right lateral views); c — M. ater, Vietnam, ZMMU S-172604 (dorsal, right lateral views); d — M. siligorensis, Vietnam, ZMMU S-167188 (ventral, left lateral views); e, f, g — M. muricola, Vietnam, ZMMU S-172616 (dorsal, right lateral views), ZMMU S-173413 (dorsal, ventrolateral, left lateral views), ZMMU S-172626 (dorsal, right lateral views); h — M. muricola, Nepal, ZMMU S-164491 (dorsal, right ventro-lateral views)

opennotspecifiedNov 2013View details →
zenodo32/100

FIG. 2 in A review of the genera Myotis, Ia, Pipistrellus, Hypsugo, and Arielulus (Chiroptera: Vespertilionidae) from Myanmar (Burma), including three species new to the country

FIG. 2. Bacula of four species of Pipistrellus. Lateral (above) and dorsal (below) views of: A — P. paterculus. MDI 12, Myanmar; B — P. javanicus. B50, Myanmar; C — P. abramus. HZM.3.32167, Vietnam; D — P. ceylonicus. HZM.3.31458, Sri Lanka, which is included to facilitate size comparisons with Fig. 1. Scale = 2 mm

opennotspecifiedAug 2005View details →
zenodo32/100

FIGURE 5 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 5. Maximum likelihood (ML) tree based on 35 cyt b sequences (1089 bp) of Myotis and outgroups. Nodes labeled with ML/BPP/NJ support values. Bayesian posterior probabilities>0.95 are designated by "*". The bootstrap values derived from 500 replications for ML/NJ trees. The sample numbers correspond to those listed in the Appendix 2 and 3.

opennotspecifiedNov 2020View details →
zenodo32/100

FIGURE 4 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 4. Bivariate scatter plot for the first and second canonical variables of a Discriminant Function analysis calculated for 22 cranial and dental measurements of 80 specimens belonging to the Myotis frater species complex. The new, Zerafshan specimen is marked with a double red circle.

opennotspecifiedNov 2020View details →
zenodo32/100

FIGURE 3 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 3. Bivariate scatter plot for the first two factors of a Principal Component analysis based on 22 cranial and dental measurements of 80 specimens belonging to the Myotis frater species complex. The new, Zerafshan specimen is marked with a double red circle.

opennotspecifiedNov 2020View details →
zenodo32/100

FIGURE 2 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 2. Live view of the new specimen of Myotis bucharensis (young male). Zerafshan Range, Tajikistan. Photo by S.V. Kruskop.

opennotspecifiedNov 2020View details →
zenodo32/100

FIGURE 1 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 1. Known distribution of M. bucharensis (squares). The new record in Zerafshan basin is shown by an open square; the type locality is marked with an asterisk.

opennotspecifiedNov 2020View details →
zenodo32/100

FIGURE 7 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 7. Maximum likelihood (ML) tree based on 27 RAG2 sequences (963 bp) of Myotis and outgroups. The bootstrap values derived from 1000 replications for ML/NJ trees. The sample numbers correspond to those listed in the Appendix 2 and 3.

opennotspecifiedNov 2020View details →
zenodo32/100

FIGURE 6 in Back to life and to taxonomy: new record and reassessment of Myotis bucharensis (Chiroptera: Vespertilionidae)

FIGURE 6. Median-joining network of the distinct cyt b haplotypes of M. longicaudatus and M. bucharensis. Each haplotype is colour-coded based on capture sites, circle size corresponds to number of samples (A). Approximate range and capture sites of M. bucharensis (orange), M. l. eniseensis (blue), M. l. longicaudatus + kaguyae (green) and M. frater (red) (B) (after Tiunov 1997; Rossina 2004, 2013; Zhigalin & Khritankov 2014; Kawai 2015; Moratelli et al. 2019).

opennotspecifiedNov 2020View details →
dryad32/100

Data from: Immune responses in hibernating little brown myotis (Myotis lucifugus) with white-nose syndrome

White-nose syndrome (WNS) is a fungal disease responsible for decimating many bat populations in North America. Pseudogymnoascus destructans (Pd), the psychrophilic fungus responsible for WNS, prospers in the winter habitat of many hibernating bat species. The immune response that Pd elicits in bats is not yet fully understood; antibodies are produced in response to infection by Pd, but they may not be protective and indeed may be harmful. To understand how bats respond to infection during hibernation, we studied the effect of Pd inoculation on the survival and gene expression of captive hibernating Myotis lucifugus with varying pre-hibernation antifungal antibody titres. We investigated gene expression through the transcription of selected cytokine genes (Il6, Il17a, Il1b, Il4 and Ifng) associated with inflammatory, Th1, Th2 and Th17 immune responses in wing tissue and lymph nodes. We found no difference in survival between bats with low and high anti-Pd titres, although anti-Pd antibody production during hibernation differed significantly between infected and uninfected bats. Transcription of Il6 and Il17a was higher in the lymph nodes of infected bats compared with uninfected bats. Increased transcription of these cytokines in the lymph node suggests that a pro-inflammatory immune response to WNS is not restricted to infected tissues and occurs during hibernation. The resulting Th17 response may be protective in euthermic bats, but because it may disrupt torpor, it could be detrimental during hibernation.

opencc-zeroDec 2016View details →
dryad32/100

Data from: Prelude to a panzootic: gene flow and immunogenetic variation in northern little brown myotis vulnerable to bat white-nose syndrome

The fungus that causes bat white-nose syndrome (WNS) recently leaped from eastern North America to the Pacific Coast. The pathogen's spread is associated with the genetic population structure of a host (Myotis lucifugus). To understand the fine-scale neutral and immunogenetic variation among northern populations of M. lucifugus, we sampled 1142 individuals across the species' northern range. We used genotypes at 11 microsatellite loci to reveal the genetic structure of, and directional gene flow among, populations to predict the likely future spread of the pathogen in the northwest and to estimate effective population size (Ne). We also pyrosequenced the DRB1-like exon 2 of the class II major histocompatibility complex (MHC) in 160 individuals to explore immunogenetic selection by WNS. We identified three major neutral genetic clusters: Eastern, Montane Cordillera (and adjacent sampling areas), and Haida Gwaii, with admixture at intermediate areas and significant substructure west of the prairies. Estimates of Ne were unexpectedly low (289–16 000). Haida Gwaii may provide temporary refuge from WNS, but the western mountain ranges are not barriers to its dispersal in M. lucifugus and are unlikely to slow its spread. Our major histocompatibility complex (MHC) data suggest potential selection by WNS on the MHC, but gene duplication limited the immunogenetic analyses.

opencc-zeroDec 2016View details →

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