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20 results for “Plecotus”
Data from: Andriollo T., Gillet F., Michaux J.R., Ruedi M. (2019). The menu varies with metabarcoding practices: A case study with the bat Plecotus auritus. PLoS ONE 14(7)
<p><strong>Supporting data for: </strong>Andriollo T., Gillet F., Michaux J.R., Ruedi M. (2019). The menu varies with metabarcoding practices: a case study with the bat <em>Plecotus auritus</em>. PLoS ONE 14(7): e0219135. https://doi.org/10.1371/journal.pone.0219135</p> <p>Raw DNA sequences of prey of <em>Plecotus auritus</em>. Sampling information separated by semicolums as folows:</p> <p>>Sequence number; Colony; Date; Sample name; Dataset; Is the sequence attributable to the diet or not (Diet); Read numbers (Size); DNA sequence</p>
Data from: Andriollo T., Ruedi M. (2018). Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland. Revue suisse de Zoologie 125(1)
<p><strong>Supporting data for:</strong> Andriollo T., Ruedi M. (2018). Novel molecular tools to identify <em>Plecotus</em> bats in sympatry. Revue suisse de Zoologie 125(1): 61-72. https://doi.org/10.5281/zenodo.1196013</p>
Figure 2 in The first record of alpine long-eared bat Plecotus macrobullaris in Serbia
Figure 2. External characters used for species identification: face and ears with tragus (A) and penis shape (B).
Figure 1 in The first record of alpine long-eared bat Plecotus macrobullaris in Serbia
Figure 1. Locality of the Plecotus macrobullaris record (black dot). Shaded parts of the map represent its distribution after the IUCN (Hutson et al. 2008). *This designation is without prejudice to positions on status, and is in line with UNSCR 1244/1999 and the International Court of Justice advisory opinion on Kosovo's declaration of independence.
Text-fig. 6. Lower jaw fragments of different fossil and recent Plecotini, occlusal view. a, b –Plecotus aff. atavus, fragment of left mnd with p4, Gritsev: a – specimen Ch/G-096; b – specimen Ch/G-104; c – P. cf. atavus, SNSB-BSPG 1962 XIX 4201, right p4, Erkertshofen 1, occlusal view; d – P. auritus, ZMMU S-174773, fragment of right mnd with p4, recent; e – P. schoepfelii, NMA P28/0478, fragment of right mnd with p4, Petersbuch 28. in The Early Miocene Bats (Chiroptera, Mammalia) From The Karstic Sites Of Erkertshofen And Petersbuch 2 (Southern Germany)
Text-fig. 6. Lower jaw fragments of different fossil and recent Plecotini, occlusal view. a, b –Plecotus aff. atavus, fragment of left mnd with p4, Gritsev: a – specimen Ch/G-096; b – specimen Ch/G-104; c – P. cf. atavus, SNSB-BSPG 1962 XIX 4201, right p4, Erkertshofen 1, occlusal view; d – P. auritus, ZMMU S-174773, fragment of right mnd with p4, recent; e – P. schoepfelii, NMA P28/0478, fragment of right mnd with p4, Petersbuch 28.
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.
Fig. 6 in Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland
Fig. 6. Close-up views of the lower mandible of Plecotus bats illustrating the shape of the chin pad in the three species. Pictures were taken from genetically identified adult long-eared bats from Switzerland or France. In the first column is P. auritus, in the middle column P. macrobullaris and in the third P. austriacus. Notice the particular shape of the chin pad of P. macrobullaris, with elongated tip and distinctly concave sides.
Fig. 5 in Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland
Fig. 5. Alignment of typical 16S sequences of different Plecotus lineages obtained with the MamP007 primer pair (framed); the expected amplicon size is 110 bp (including primers). Alignment dots represent identical nucleotides.
Fig. 4 in Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland
Fig. 4. Bivariate plot of the length of upper tooth row (CM3) versus diameter of tympanic bulla (DBT) of 194 skulls of Plecotus. Blue squares represent skulls of P. auritus, violet circles skulls of P. macrobullaris and orange triangles skulls of P. austriacus. Plain symbols indicate genetically identified individuals, while hollow ones are from animals examined for skull morphology only. Coloured boxes indicate the species-specific measurement ranges given by Benda & Ivanova (2003) for Central European Plecotus and the grey bars represent the limit values of the two cranial measurements proposed by Blant et al. (2008) to identify the three species.
Fig. 3 in Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland
Fig. 3. Map of Switzerland depicting the six biogeographical regions occurring in this country (Gonseth et al., 2001) and the occurrences of 700 genetically identified Plecotus samples. Plain symbols represent locations of P. auritus (in blue), P. austriacus (in orange) and P. macrobullaris (in violet). Symbols with more than one colour represent areas of sympatry. Map produced by the Centre Suisse de Cartographie de la Faune.
Fig. 2 in Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland
Fig. 2. Species-specific patterns of amplification of 16S fragments obtained in a single PCR cocktail. These fragments were resolved on a 1.6% agarose gel run for about 30 min at 60 V/m. A 100 bp molecular ladder was run on each side of the pictured agarose gel. Amplification products of diagnostic sizes appear on lane 1 for P. macrobullaris (at about 400 bp), on lane 2 for P. austriacus (350 bp), on lane 3 for the 'west' clade of P. auritus (300 bp) and on lane 4 for the 'east' clade of P. auritus (two bands at about 300 and 400 bp, respectively).
Fig. 1 in Novel molecular tools to identify Plecotus bats in sympatry and a review of their distribution in Switzerland
Fig. 1. Skull drawing of a Plecotus austriacus (specimen MHNG 1704.016) illustrating the two cranial measurements examined in this study (DBT and CM3).
Figure 3 in The first record of alpine long-eared bat Plecotus macrobullaris in Serbia
Figure 3. Photographs of skull in dorsal (A), ventral (B), and lateral (C) view.
On following pages: 228. Christie's Long-eared Bat (Plecotus christii); 229. Mediterranean Long-eared Bat (Plecotus turkmenicus); 232. Strelkov's Long-eared Bat (Plecotus strelkovi); 233. Ognev's Long-eared Bat (Plecotus ognevi); Long-eared Bat (Plecotus homochrous); 237. Taiwan Long-eared Bat (Plecotus taivanus); 238. Japanese Long-eared macrobullaris); 241. Sardinian Long-eared Bat (Plecotus sardus); 242. Brown Long-eared Bat (Plecotus auritus); 243 245. Rafinesque's Big-eared Bat (Corynorhinus rafinesquii); 246. Townsend's Big-eared Bat (Corynorhinus townsendii kolombatovici); 230. Ethiopian Long-eared Bat (Plecotus balensis); 231. Turkmen Long-eared Bat (Plecotus 234. Kozlov's Long-eared Bat (Plecotus kozlovi); 235. Sichuan Long-eared Bat (Plecotus ariel); 236. Himalayan Bat (Plecotus sacrimontis); 239. Ward's Long-eared Bat (Plecotus ward): 240. Alpine Long-eared Bat (Plecotus. Desert Long-eared Bat (Otonycteris hemprichii); 244. Turkestani Long-eared Bat (Otonycteris leucophaea) '); 247. Mexican Big-eared Bat (Corynorhinus mexicanus); 248. Allen's Big-eared Bat (/dionycteris phyllotis). in Vespertilionidae
On following pages: 228. Christie's Long-eared Bat (Plecotus christii); 229. Mediterranean Long-eared Bat (Plecotus turkmenicus); 232. Strelkov's Long-eared Bat (Plecotus strelkovi); 233. Ognev's Long-eared Bat (Plecotus ognevi); Long-eared Bat (Plecotus homochrous); 237. Taiwan Long-eared Bat (Plecotus taivanus); 238. Japanese Long-eared macrobullaris); 241. Sardinian Long-eared Bat (Plecotus sardus); 242. Brown Long-eared Bat (Plecotus auritus); 243 245. Rafinesque's Big-eared Bat (Corynorhinus rafinesquii); 246. Townsend's Big-eared Bat (Corynorhinus townsendii kolombatovici); 230. Ethiopian Long-eared Bat (Plecotus balensis); 231. Turkmen Long-eared Bat (Plecotus 234. Kozlov's Long-eared Bat (Plecotus kozlovi); 235. Sichuan Long-eared Bat (Plecotus ariel); 236. Himalayan Bat (Plecotus sacrimontis); 239. Ward's Long-eared Bat (Plecotus ward): 240. Alpine Long-eared Bat (Plecotus. Desert Long-eared Bat (Otonycteris hemprichii); 244. Turkestani Long-eared Bat (Otonycteris leucophaea) '); 247. Mexican Big-eared Bat (Corynorhinus mexicanus); 248. Allen's Big-eared Bat (/dionycteris phyllotis).
Figure 2 in A multidisciplinary approach unveils the distribution of the Alpine long-eared bat Plecotus macrobullaris (Vespertilionidae) in Italy
Figure 2: Phylogenetic analyses of long-eared bats. (Left) origin of molecular samples analysed from Italy; (right) bootstrapped consensus ML phylogenetic tree (10,000 iterations) obtained from the analysis of COI gene fragment of Plecotus bats. Coloured sequences represent new genetic sequences and refer to different species. The statistical support of major clades is shown at their nodes (ML bootstrap support).
Figure 1 in A multidisciplinary approach unveils the distribution of the Alpine long-eared bat Plecotus macrobullaris (Vespertilionidae) in Italy
Figure 1: Summary of the distribution of the Alpine long-eared bat in Italy. Colour coding: yellow, non-genotyped (scientific and grey literature); orange, non-genotyped (new occurrences); purple, genotyped.
Data from: The foraging ecology of the Mountain long-eared bat Plecotus macrobullaris revealed with DNA mini-barcodes
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Data from: Aerodynamics of manoeuvring flight in brown long-eared bats (Plecotus auritus)
In this study, we explicitly examine the aerodynamics of manoeuvring flight in animals. We studied brown long-eared bats flying in a wind tunnel while performing basic sideways manoeuvres. We used particle image velocimetry in combination with high-speed filming to link aerodynamics and kinematics to understand the mechanistic basis of manoeuvres. We predicted that the bats would primarily use the downstroke to generate the asymmetries for the manoeuvre since it has been shown previously that the majority of forces are generated during this phase of the wingbeat. We found instead that the bats more often used the upstroke than they used the downstroke for this. We also found that the bats used both drag/thrust-based and lift-based asymmetries to perform the manoeuvre and that they even frequently switch between these within the course of a manoeuvre. We conclude that the bats used three main modes: lift asymmetries during downstroke, thrust/drag asymmetries during downstroke and thrust/drag asymmetries during upstroke. For future studies, we hypothesize that lift asymmetries are used for fast turns and thrust/drag for slow turns and that the choice between up- and downstroke depends on the timing of when the bat needs to generate asymmetries.
Supplementary material 1 from: Luo P, He X, Zhang Y, Ye J, Guo M, Deng J, Zhou C, Zhou J, Zhang L (2023) Confirmation of the existence of Himalayan long-eared bats, Plecotus homochrous (Chiroptera, Vespertilionidae), in China. ZooKeys 1161: 129-141. https://doi.org/10.3897/zookeys.1161.99487
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Data from: Aerodynamics of manoeuvring flight in brown long-eared bats (Plecotus auritus)
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