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    <identifier>10.57760/sciencedb.38857</identifier>
    <datestamp>2026-06-08T11:35:56Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2026-06-08</dc:date>
  <dc:title>New records and an updated checklist of the genus Myotis (Chiroptera, Vespertilionidae) in Xizang, China</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.38857</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Morphological data collectionFollowing the Chiroptera Morphometric Standard (Yang et al., 2007), 5 external and 13 craniodental characteristics (Table 2; Supplementary Table S2) were taken using MNT-150 digital calipers (Meinert Industrial Co., Ltd., China; accuracy 0.01 mm). External measurements included forearm length (FA); tibia length (TIB); hindfoot length including claw (HF); ear length (EL); and tail length (TL). Craniodental measurements comprised: greatest length of skull (GTL); condylocanine length (CCL); zygomatic breadth (ZB); mastoid width (MAW); braincase width (BCW); height of braincase (BCH); palatal bridge length (PBL); maxillary toothrow length (C1M3L); upper canine width (C1C1W); width across the upper molars (M3M3W); mandibular toothrow length (C1M3L); mandible length (ML); and mandibular height (MH). Missing values were absent in our morphometric dataset.Genetic data (cyt b) acquisitionTotal genomic DNA was extracted from approximately 20 mg of muscle tissue using a commercial kit (DNU333-03, Maibao Biotechnology Co., Ltd., China). The mitochondrial cytochrome b (cyt b) gene was amplified by PCR using primers from Irwin et al. (1991) and Ruedi et al. (2013). Each 30 &amp;micro;L reaction contained: 13 &amp;micro;L of 2&amp;times;Accurate Taq Premix (AG11009, Accurate Biotechnology Co., Ltd., China), 0.5 &amp;micro;L of each forward and reverse primer (10 &amp;micro;mol/L), 14 &amp;micro;L of RNase-free water, and 2 &amp;micro;L of DNA template (~20 ng/&amp;micro;L). Thermal cycling profile was: initial denaturation at 94 &amp;deg;C for 5 min; 37 cycles of 94 &amp;deg;C for 45 s, 46 &amp;deg;C for 30 s, and 72 &amp;deg;C for 60 s; and a final extension at 72 &amp;deg;C for 5 min. Amplification products were verified by agarose gel electrophoresis and submitted to Sangon Biotech (Shanghai) for bidirectional Sanger sequencing. The 18 newly generated cyt b sequences from this study.Echolocation call recordingEcholocation calls of Myotis bats were recorded in flight state using an ultrasound detector (M500-384, Pettersson Elektronik AB, Sweden). Recordings were conducted in a quiet room (approximately 3 m&amp;times;3 m&amp;times;3 m). Acoustic data were analyzed using BatSound v.4.0 (sampling frequency: 300 kHz, Fast Fourier Transform (FFT) size: 1024 points). For each species, more than 10 high-quality pulses were selected to measure three key parameters: peak frequency, pulse duration, and inter-pulse interval. Given that the Myotis calls typically consist of broadband frequency-modulated (FM) signals with multiple harmonics, where the first harmonic is the strongest and other harmonics (2nd&amp;ndash;4th) decrease successively, only the first harmonic was analyzed in this study.</dc:description>
  <dc:subject>Xizang (China); New records; Myotis; Species diversity; Taxonomic revision</dc:subject>
  <dc:creator>Kun-Hao Chen</dc:creator>
  <dc:creator>Yang Guo</dc:creator>
  <dc:creator>Yong-Xin Miao</dc:creator>
  <dc:creator>Lin-Ying Xue</dc:creator>
  <dc:creator>Yi Wu</dc:creator>
  <dc:creator>Yang Yue</dc:creator>
  <dc:creator>Li-Biao Zhang</dc:creator>
  <dc:creator>Wen-Hua Yu</dc:creator>
  <dc:creator>Xiao-Yun Wang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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