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11 results for “Barbastella”
Text-fig. 5. Upper molars of different fossil and recent Plecotini, occlusal view. a – Plecotus cf. atavus, PCMRCh3, left M1, Petersbuch 2; b – P. aff. atavus, Ch/G-175, left M1, Gritsev; c – P. auritus, ZMMU S-174773, right M1, recent; d – P. schoepfelii, NMA P62/0114, right M2, Petersbuch 62; e – Corynorhinus townsendii, ZMMU S-105677, right M1, recent; f – Barbastella maxima, Ch/G-001, right M1, Gritsev. in The Early Miocene Bats (Chiroptera, Mammalia) From The Karstic Sites Of Erkertshofen And Petersbuch 2 (Southern Germany)
Text-fig. 5. Upper molars of different fossil and recent Plecotini, occlusal view. a – Plecotus cf. atavus, PCMRCh3, left M1, Petersbuch 2; b – P. aff. atavus, Ch/G-175, left M1, Gritsev; c – P. auritus, ZMMU S-174773, right M1, recent; d – P. schoepfelii, NMA P62/0114, right M2, Petersbuch 62; e – Corynorhinus townsendii, ZMMU S-105677, right M1, recent; f – Barbastella maxima, Ch/G-001, right M1, Gritsev.
On following pages: 204. Van Gelder's Bat (Bauerus dubiaquercus); 205. Pallid Bat (Antrozous pallidus); 206. Black-winged Little Yellow Bat (Rhogeessa tumida); 207. Yucatan Yellow Bat (Rhogeessa aenea): 208. Bickham's Yellow Bat (Rhogeessa bickhami); 209. Menchu''s Yellow Bat (Rhogeessa menchuae); 210. Ecuadorian Little Yellow Bat (Rhogeessa velilla); 211. Tiny Yellow Bat (Rhogeessa minutilla); 212. Genoways's Yellow Bat (Rhogeessa genowaysi); 213. Thomas's Yellow Bat (Rhogeessa io); 214. Northern Little Yellow Bat (Rhogeessa parvula); 215. Least Yellow Bat (Rhogeessa mira); 216. Allen's Yellow Bat (Rhogeessa alleni); 217. Slender Yellow Bat (Rhogeessa gracilis); 218. Husson's Yellow Bat (Rhogeessa hussoni); 219. Western Barbastelle (Barbastella barbastellus); 220. Caspian Barbastelle (Barbastella caspica); 221. Arabian Barbastelle (Barbastella leucomelas): 222. Eastern Barbastelle (Barbastella darjelingensis); 223. Japanese Barbastelle (Barbastella pacifica); 224. Beijing Barbastelle (Barbastella beijingensis). in Vespertilionidae
On following pages: 204. Van Gelder's Bat (Bauerus dubiaquercus); 205. Pallid Bat (Antrozous pallidus); 206. Black-winged Little Yellow Bat (Rhogeessa tumida); 207. Yucatan Yellow Bat (Rhogeessa aenea): 208. Bickham's Yellow Bat (Rhogeessa bickhami); 209. Menchu''s Yellow Bat (Rhogeessa menchuae); 210. Ecuadorian Little Yellow Bat (Rhogeessa velilla); 211. Tiny Yellow Bat (Rhogeessa minutilla); 212. Genoways's Yellow Bat (Rhogeessa genowaysi); 213. Thomas's Yellow Bat (Rhogeessa io); 214. Northern Little Yellow Bat (Rhogeessa parvula); 215. Least Yellow Bat (Rhogeessa mira); 216. Allen's Yellow Bat (Rhogeessa alleni); 217. Slender Yellow Bat (Rhogeessa gracilis); 218. Husson's Yellow Bat (Rhogeessa hussoni); 219. Western Barbastelle (Barbastella barbastellus); 220. Caspian Barbastelle (Barbastella caspica); 221. Arabian Barbastelle (Barbastella leucomelas): 222. Eastern Barbastelle (Barbastella darjelingensis); 223. Japanese Barbastelle (Barbastella pacifica); 224. Beijing Barbastelle (Barbastella beijingensis).
FIGURE 6 in Taxonomic status of the barbastelles (Chiroptera: Vespertilionidae: Barbastella) from the Japanese archipelago and Kunashir Island
FIGURE 6. Skulls of the newly describing Barbastella species: a—Barbastella pacifica sp. nov., holotype BSI 168-07, adult male, Kunashir Island; b—Barbastella pacifica sp. nov., NSMT M-8774, female, Honshu, Saitama; c—B. leucomelas, NMP PB2883, adult male, Egypt, Sinai; d—B. cf. darjelingensis, ZMMU S-186685, adult male, Vietnam, Lao Cai. Scale bar 5 mm.
FIGURE 4 in Taxonomic status of the barbastelles (Chiroptera: Vespertilionidae: Barbastella) from the Japanese archipelago and Kunashir Island
FIGURE 4. Bivariate scatter plot for the First and Second Canonical Variances calculated in Discriminant Function analysis for 18 cranial and dental measurements of 117 Barbastella specimens.
FIGURE 3 in Taxonomic status of the barbastelles (Chiroptera: Vespertilionidae: Barbastella) from the Japanese archipelago and Kunashir Island
FIGURE 3. Bivariate scatter plots for the PC analyses of putative and accepted Barbastella species; Factors (Principal Components) are calculated from the 17 cranial and dental measurements in total for 117 specimens; analyzes were performed independently for each pair of species.
FIGURE 5 in Taxonomic status of the barbastelles (Chiroptera: Vespertilionidae: Barbastella) from the Japanese archipelago and Kunashir Island
FIGURE 5. Penial bones of barbastelles: a–c—B. barbastellus (a, b—Russia, Krasnodar territory, ZMMU S-169241, S- 169265; c—Czech Republic, n/n); d–e—B. caspica, (d—Tajikistan, ZMMU S-169301; e—Kirghizstan, CUP CT84/253); f—B. leucomelas, Egypt, Sinai, NMP 90521; g—B. darjelingensis, Nepal, Annapurna Himalaya, ZMMU S-164496; h—B. cf. darjelingensis, Vietnam, Lao Cai province, ZMMU S-186685; i–k—B. pacifica sp. nov. (i, j—Japan, Nagano prefecture, NSMT M-52949, 52944; k—Japan, Hokkaido, NSMT M-18559); c, e and f adopted from Benda et al. 2008; k—from Yoshiyuki 1989; others—original. Scale bar 1 mm.
FIGURE 2 in Taxonomic status of the barbastelles (Chiroptera: Vespertilionidae: Barbastella) from the Japanese archipelago and Kunashir Island
FIGURE 2. Phylogenetic relationships of Barbastella sp. n. based on A) ND1 sequences (929bp), B) partial cytb (609bp) sequences and C) COI (523bp) sequences. The scale indicates genetic distance estimated by the Kimura 2-parameter method on the NJ tree. The bootstrap values derived from 1000 replication for NJ tree / maximum likelihood probabilities. Specimens of Plecotus auritus (ND1 HM164052; COI JF443099) or P. sacrimontis (Cytb OCUM5351) were used as an outgroup. The sample numbers correspond to those in the Appendix (Tables A1, A2).
FIGURE 1 in Taxonomic status of the barbastelles (Chiroptera: Vespertilionidae: Barbastella) from the Japanese archipelago and Kunashir Island
FIGURE 1. Distribution of barbastelles (adopted from the IUCN Red List (www.iucnredlist.org); with additions from Smith & Xie 2008; Benda et al. 2012; 2015; Fukui 2015). Red—Barbastella barbastellus, dark blue—B. caspica, light blue—B. leucomelas, magenta—B. darjelingensis sensu stricto, green—B. cf. darjelingensis, light brown—B. n. sp. Full symbols mark material genotyped by at least one gene; open symbols—specimens included into morphological study only. Type localities of named taxa: 1—darjelingensis Hodgson, 1855; 2—caspica Satunin, 1908; 3—walteri Bianchi, 1916; 4—leucomelas Cretzschmar, 1826; 5—beijingensis Zang et al., 2008; 6—barbastellus Schreber, 1774; 7—guanchae Trujillo, Ibáñez and Juste, 2002.
FIG. 3. Video stills showing B in CCTV enables the discovery of new barbastelle (Barbastella barbastellus) vocalisations and activity patterns near a roost
FIG. 3. Video stills showing B. barbastellus activity near the roost, the entrance of which is in the bottom third of the images. The bats are filmed with infrared light. A) A single bat investigates the roost tree, filmed from the side of the roost tree. This bat was moving slowly, and the image is sharp; B) Four swarming bats, filmed facing the roost entrance. As the bats move at speed when swarming, they appear blurred in a single video frame
FIG. 2 in CCTV enables the discovery of new barbastelle (Barbastella barbastellus) vocalisations and activity patterns near a roost
FIG. 2. Histogram showing the number of spectrograms associated with B. barbastellus swarming around a roost, produced for each time interval from June to September 2016
FIG. 1. Call spectrograms for B in CCTV enables the discovery of new barbastelle (Barbastella barbastellus) vocalisations and activity patterns near a roost
FIG. 1. Call spectrograms for B. barbastellus close to the roost. A) Standard pass echolocation, showing lower frequency type 1 and higher frequency type 2 pulses alternating, then followed by type 1 pulses only; B) Approach echolocation pulse group produced by a single bat approaching the roost tree entrance. In each case, pulse analysis was based on the central group of five pulses: pulses 3 to 7 from the left in this case. This example shows a group of lower frequency pulses on the far right, typical of a bat approaching the tree very closely; C) Swarming echolocation recorded with two bats in flight close to the roost. These are broadband pulses with second harmonics. Pulses do not appear in a fixed pattern as with approach echolocation, but tend to be produced in a dynamic group. It is not possible to determine from which bat successive pulses originated; D) Swarming honking recorded with five bats in flight round the roost tree. These are similar to swarming echolocation pulses but with a high amplitude quasi-constant frequency (QCF) tail, apparently to communicate with bats on a collision course; E) Hooked social calls recorded just before swarming activity with five bats. The straighter pulses next to the hooked calls were presumably produced by a different bat
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