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207 results for “Rhinolophus”
Fig. 14. Rhinolophus alcyone AMNH 236298 in The Chiropteran Premaxilla: A Reanalysis of Morphological Variation and Its Phylogenetic Interpretation
Fig. 14. Rhinolophus alcyone AMNH 236298, dorsal view of the rostrum. Scale 5 1 mm. Abbreviations: a wedge-shaped gap between left and right premaxillary bodies; bp body of the premaxilla; C upper canine; I2 second upper incisor; ifo incisive foramen; lfpp lateral flange of the palatine process of the premaxilla; mfpp medial flange of the palatine process of the premaxilla; mx maxilla.
Fig. 13. Rhinolophus ferrumequinum nippon AMNH 245591 in The Chiropteran Premaxilla: A Reanalysis of Morphological Variation and Its Phylogenetic Interpretation
Fig. 13. Rhinolophus ferrumequinum nippon AMNH 245591, digital rendering constructed from CT-scan images, rostrodorsolateral (A) and rostrodorsal (B) views of the skull. Scale 5 5 mm. Abbreviations: bp body of premaxilla; C upper canine; I2 second upper incisor; ino incisive notch; ppmx palatine process of premaxilla.
Data from: Integrating population genetics to define conservation units from the core to the edge of Rhinolophus ferrumequinum western range
The greater horseshoe bat (<i>Rhinolophus ferrumequinum</i>) is among the most widespread bat species in Europe but it has experienced severe declines, especially in Northern Europe. This species is listed Near Threatened in the European IUCN Red List of Threatened Animals and it is considered to be highly sensitive to human activities and particularly to habitat fragmentation. Therefore, understanding the population boundaries and demographic history of populations of this species is of primary importance to assess relevant conservation strategies. In this study, we used 17 microsatellite markers to assess the genetic diversity, the genetic structure and the demographic history of <i>R. ferrumequinum</i> colonies in the western part of its distribution. We identified one large population showing high levels of genetic diversity and large population size. Lower estimates were found in England and northern France. Analyses of clustering and isolation by distance suggested that the Channel and the Mediterranean seas could impede <i>R. ferrumequinum</i> gene flow. These results provide important information to improve the delineation of <i>R. ferrumequinum</i> management units. We suggest that a large management unit corresponding to the population ranging from Spanish Basque country to northern France must be considered. Particular attention should be given to mating territories as they seem to play a key role in maintaining the high levels of genetic mixing between colonies. Smaller management units corresponding to English and northern France colonies must also be implemented. These insular or peripheral colonies could be at higher risk of extinction in a near future.
Fig. 1 in New record of Rhinolophus chiewkweeae (Chiroptera: Rhinolophidae) from the east coast of Peninsular Malaysia with new information on their echolocation calls, genetics and their taxonomy
Fig. 1. Latero-ventral view of Rhinolophus chiewkweeae, from Sungai Buweh, Lawit
Data from: Integrating population genetics to define conservation units from the core to the edge of Rhinolophus ferrumequinum western range
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On following pages: 94. Thomas's Horseshoe Bat (Rhinolophus thomasi); 95. Lesser Horseshoe Bat (Rhinolophus hipposideros); 96. rancis's Woolly Horseshoe Bat (Rhinolophus trancisi); 97. Lesser Woolly Horseshoe Bat (Rhinolophus sedulus); 98. Trefoil Horseshoe Bat (Rhinolophus trifoliatus); 99. Northern Woolly Horseshoe Bat (Rhinolophus perniger); 100. Selangor Woolly Horseshoe Bat (Rhinolophus luctoides); 101. Malaysian Woolly Horseshoe Bat (Rhinolophus mono); 102. Great Woolly Horseshoe Bat (Rhinolophus luctus); 1.03. Beddome's Woolly Horseshoe Bat (Rhinolophus beddomei); 104. Formosan Woolly Horseshoe Bat (Rhinolophus formosaë); 105. Thailand Horseshoe Bat (Rhinolophus thailandensis); 106. Dobson's Horseshoe Bat (Rhinolophus yunanensis); 107. Chiew Kwee's Horseshoe Bat (Rhinolophus chiewkweeae); 108. Pearson's Horseshoe Bat (Rhinolophus pearsonii); 109. Mitred Horseshoe Bat (Rhinolophus mitratus). in Rhinolophidae
On following pages: 94. Thomas's Horseshoe Bat (Rhinolophus thomasi); 95. Lesser Horseshoe Bat (Rhinolophus hipposideros); 96. rancis's Woolly Horseshoe Bat (Rhinolophus trancisi); 97. Lesser Woolly Horseshoe Bat (Rhinolophus sedulus); 98. Trefoil Horseshoe Bat (Rhinolophus trifoliatus); 99. Northern Woolly Horseshoe Bat (Rhinolophus perniger); 100. Selangor Woolly Horseshoe Bat (Rhinolophus luctoides); 101. Malaysian Woolly Horseshoe Bat (Rhinolophus mono); 102. Great Woolly Horseshoe Bat (Rhinolophus luctus); 1.03. Beddome's Woolly Horseshoe Bat (Rhinolophus beddomei); 104. Formosan Woolly Horseshoe Bat (Rhinolophus formosaë); 105. Thailand Horseshoe Bat (Rhinolophus thailandensis); 106. Dobson's Horseshoe Bat (Rhinolophus yunanensis); 107. Chiew Kwee's Horseshoe Bat (Rhinolophus chiewkweeae); 108. Pearson's Horseshoe Bat (Rhinolophus pearsonii); 109. Mitred Horseshoe Bat (Rhinolophus mitratus).
FIG. 12 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 12. Distribution of COI clades of R. affinis in the Sundaic subregion. The shape of the symbols corresponds to clades defined in Fig. 11. Black symbols are sequences from the current study and Ith et al. (in review) whereas grey symbols are sequences from GenBank. Localities of the sequences not listed in the methods and materials of the current study are listed for the first time as following, ER = Endau Rompin National Park, Peninsular Malaysia; KL = Kuala Lompat, Pahang; NS = Negeri-Sembilan; TT = Thaninthary Div, Myanmar. Dashed arrows indicate the type localities of subspecies. Black solid arrows indicate the transition zones of biota in the peninsula
FIG. 11 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 11. Maximum likelihood tree based on COI. Scores on the branches refer to bootstrap support values (1,000 iterations) derived from maximum likelihood (1st score) and Bayesian posterior probabilities (2nd score); -- = no support value. Specimens are labeled by specimen codes (IS, HM, HZM and MZB) and collecting localities. The symbols of clades correspond to the genetic distribution map, Fig. 12
FIG. 9 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 9. Baysian phylogenetic tree based on Cytb gene. Scores on the branches refer to bootstrap support values (1,000 iterations) derived from maximum likelihood (1st score) and Bayesian posterior probabilities (2nd score); -- = no support value. The horizontal bars on the tree branches represent the 95% highest posterior density intervals for the divergence estimates. Specimens are labeled by specimen codes (CHGTK, EF, EU, JN, IS, MZB, PS and TK) and collecting localities. The symbols of clades correspond to the genetic distribution map, Fig. 10
FIG. 10 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 10. Distribution of Cytb clades of R. affinis within the Sundaic subregion. The shape of the symbols corresponds to clades defined in Fig. 9. Black symbols are sequences from the current study whereas grey symbols are sequences from GenBank. Localities of sequences not listed in the methods and materials of the current study are listed for the first time as following, BA = Jambusan Cave, Bau, Sarawak; GB = Gunung Berumput, Sarawak; GG = Gunung Gading NP, Sarawak; KM = Kabumen, Central Java and PC = Prachuap Kiri Khan. unK = unknown specific locality from Borneo (sequences from GenBank). Dashed arrows indicate the type localities of subspecies. Black solid arrows indicate the transition zones of biota in the peninsula
Fig. 2 in A New Horseshoe Bat, Rhinolophus chiewkweeae (Chiroptera, Rhinolophidae), from Malaysia
Fig. 2. Head of Rhinolophus chiewkweeae sp. nov., paratype, NSMT-M33471, male (top) and dorsal aspect of Rhinolophus chiewkweeae sp. nov., holotype, NSMT-M33472, female (bottom)
FIG. 6 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 6. Dorsal view of R. affinis skulls from Borneo (A — TK168483, ♀), Sumatra (B — MZB35882, ♀), Java (C — MZB34475, ♀), Malay Peninsula (D — IS110823.10, ♂; E — IS120122.1, ♂) and India (F — HZM4.28148, ♂). Scale = 5 mm
FIG. 8 in Hill forest dweller: a new cryptic species of Rhinolophus in the 'pusillus group' (Chiroptera: Rhinolophidae) from Thailand and Lao PDR
FIG. 8. Bayesian tree based on based on 41 cyt b sequences of bats from East and Southeast Asia using GTR+I+G model. The node labels indicate posterior probability values. The genetic distances within and between species are presented in Table 5. Specimens included in this analysis are listed in Appendix II
FIG. 5 in Hill forest dweller: a new cryptic species of Rhinolophus in the 'pusillus group' (Chiroptera: Rhinolophidae) from Thailand and Lao PDR
FIG. 5. Dorsal (left) and lateral views (right) of the baculum of (a) R. monticolus sp. nov. PSUZC-MM2013.14 (paratype) from Thailand, and (b) R. shortridgei PSUZC-MM2010.7 from Myanmar. Scale bar = 2 mm
FIG. 4 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 4. Noseleaf variation of R. affinis in the Sundaic subregion (specimen from northern India included for comparison). Kabumen, Central Java (A — MZB34475, ♀); Musoorie, northern India (B — HZM.4.28148, ♂); Sarawak, northwest Borneo (C — TK152216, ♀); Lampung, southwestern Sumatra (D — MZB34965, ♀); Narathiwat, southern Malay Peninsula (E — IS120122.1, ♂); Songkhla, southern Malay Peninsula (F — IS110823.10, ♂). Scale = 5 mm
FIG. 9 in Hill forest dweller: a new cryptic species of Rhinolophus in the 'pusillus group' (Chiroptera: Rhinolophidae) from Thailand and Lao PDR
FIG. 9. Bayesian tree based on 183 COI sequences of bats from East and Southeast Asia using GTR+I+G model. The node labels indicate posterior probability values. The genetic distances within and between species are presented in Table 6. For the pusillus- group, the country names where specimens were collected are given. Specimens included in this analysis are listed in Appendix III
FIG. 4 in Hill forest dweller: a new cryptic species of Rhinolophus in the 'pusillus group' (Chiroptera: Rhinolophidae) from Thailand and Lao PDR
FIG. 4. Occlusal view of the upper and lower toothrows of (a) R. monticolus sp. nov. ♂ PSUZC-MM2008.1 (holotype) from Thailand, and (b) R. shortridgei ♂ BMNH. 18.8.3.1 (holotype) from Myanmar. Scale bar = 5 mm
FIG. 3 in Hill forest dweller: a new cryptic species of Rhinolophus in the 'pusillus group' (Chiroptera: Rhinolophidae) from Thailand and Lao PDR
FIG. 3. Lateral and dorsal views of the skull of (a) R. monticolus sp. nov. ♂ PSUZC-MM2008.1 (holotype) from Thailand, and (b) R. shortridgei ♂ BMNH. 18.8.3.1 (holotype) from Myanmar. Scale bar = 5 mm
FIG. 2 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 2. PCA of 12 external and cranial characters for R. affinis specimens from Borneo (black squares), Sumatra (black diamonds), southern Malay Peninsula (black circles) and northern Malay Peninsula (open circles)
FIG. 2 in Hill forest dweller: a new cryptic species of Rhinolophus in the 'pusillus group' (Chiroptera: Rhinolophidae) from Thailand and Lao PDR
FIG. 2. Noseleaf (a–c) and dorsal (d) and ventral (e) pelage of R. monticolus sp. nov. PSUZC-MM2013.14 (paratype) from Thailand. Not to scale
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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