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Figure 1 in Bats can migrate farther than it was previously known: a new longest migration record by Nathusius' pipistrelle Pipistrellus nathusii (Chiroptera: Vespertilionidae)
Figure 1: Long-distance movement of a Nathusius' pipistrelle Pipistrellus nathusii from Borok (Russia) to Lully (France).
Figure 1 in Into the light: atypical diurnal foraging activity of Blyth's horseshoe bat, Rhinolophus lepidus (Chiroptera: Rhinolophidae) on Tioman Island, Malaysia
Figure 1: Map showing Tioman Island in the State of Pahang, Peninsular Malaysia, along with locations of villages and Tekok-Juara trail where day-flying RHiNOlOpHus lepidus was recorded.
Fig. 7 in Fossil Evidence and the Origin of Bats
Fig. 7. Compilation of microchiropteran taxa from the Oligocene through Pliocene. Top graph represents the number of genera recognized from the Old and New Worlds, bottom graph shows the percentage of these taxa that represent modern genera. Note that by the Pliocene almost all known fossil bats belong to modern genera.
Fig. 5 in Fossil Evidence and the Origin of Bats
Fig. 5. Distribution of Eocene bats in Europe. Note the increased presence of modern bat families from the middle Eocene onward.
Fig. 3 in Fossil Evidence and the Origin of Bats
Fig. 3. Specimen of Hassianycteris messelensis (SMF ME 1414a) from Messel Oil Shale, middle Eocene, Germany (photo courtesy of J. Habersetzer, imagine taken by E. Pantak).
Fig. 2 in Fossil Evidence and the Origin of Bats
Fig. 2. Holotype specimen of Icaronycteris index (YPM-PU 18150) from the Green River Formation, early Eocene, southwestern Wyoming.
Figure 3 in The heterogeneity of Caatinga biome: an overview of the bat fauna
Figure 3: Cluster analyses based on the Euclidean distance for the bat species composition in the eight Caatinga ecoregions (A) and for the main references in the best surveyed ecore- gions for the bat fauna. (B) * Fazenda Arara/Caatinga Arbustiva ** Reserva Particular do Patrimônio Natural – Fazenda Bituri/ Floresta Montana. Chapada Diamantina Complex (CDC), São Francisco Dunes (SFD), Raso da Catarina (RAC), Campo Maior Complex (CMC), Borborema Highlands (BOH), Southern Sertaneja Depression (SSD), Ibiapaba-Araripe Complex (IAC), and Northern Sertaneja Depression (NSD).
Figure 2 in The heterogeneity of Caatinga biome: an overview of the bat fauna
Figure 2: Scatter plot showing the relationship between the number of bat species known to each Caatinga ecoregion and (A) the ecoregion area and (B) the number of studies that included the sampling of chiropterans in each ecoregion.
Fig. 1. A in Fossil Evidence and the Origin of Bats
Fig. 1. A strict consensus of four equally parsimonious trees (791 steps each) derived from analysis of our new morphological dataset. Numbers above the branches are decay values; those below the branches are bootstrap values. In each pair of numbers, the first number represents the support value calculated using the complete dataset; the second number represents the support value calculated in an analysis including all taxa except Tanzanycteris, a relatively poorly known fossil. Most decay and bootstrap values were generally unaffected by removal of Tanzanycteris. However, support for some nodes in the middle of the tree increased markedly when Tanzanycteris was removed (i.e., for the crown group Microchiroptera the decay value increased from one to four, and the bootstrap from 37 to 76%).
Figure 1 in The heterogeneity of Caatinga biome: an overview of the bat fauna
Figure 1: Map of Caatinga ecoregions and municipalities surveyed for chiropteran fauna. Inset shows the South American continent and Brazil, more specifically northeastern Brazil (light gray) and the area covered by the Caatinga biome (dark gray). The numbers indicate the names of municipalities, as follows. Superscript numbers in brackets indicate the studies that cite the municipality, as listed in Supplementary Table S1. 1 – Batalha – PI (39); 2 – José de Freitas – PI (36); 3 – Teresina – PI (28;35;54); 4 – Monsenhor Gil – PI (25); 5 – Arajara – CE (23,64); 6 – Crateús – CE (4;21;52); 7 – Crato – CE (23;28;55;60;61); 8 – Ipu – CE (57); 9 – Juazeiro do Norte – CE (2); 10 – Nova Olinda – CE (53;28); 11 – Parambú – CE (24); 12 – Ubajara – CE (20;50); 13 – Cocal – PI (25); 14 – Guaribas – PI (19); 15 – São Raimundo Nonato – PI (28); 16 – Valença do Piauí – PI (28;61); 17 – Canindé – CE (7;8); 18 – Fortaleza – CE (7;27;63); 19 – Guaramiranga – CE (7;63); 20 – Jaguaruana – CE (7; 8); 21 – Limoeiro do Norte – CE (7;8;32); 22 – Morada Nova – CE (7); 23 – Palhano – CE (7); 24 – Pereiro – CE (7;8); 25 – Quixadá – CE (2;7;8;32;63); 26 – Russas – CE (7;8;32); 27 – Brejo dos Santos – PB (10); 28 – Maturéia – PB (32); 29 – Santa Terezinha – PB (10;32); 30 – São José dos Cordeiros – PB (10;13;32); 31 – Pombal – PB (32); 32 – Exu – PE (2;18;23;28;53;60;61); 33 – Apodi – RN (12); 34 – Baraúna – RN(12); 35 – Felipe Guerra – RN (12); 36 – Martins – RN (12); 37 – Mossoró – RN (5); 38 – Nova Cruz – RN (11;32); 39 – Pedra Grande – RN (12); 40 – Alagoinha – PB (32); 41 – Araruna – PB (4;9; 10;32); 42 – Areia – PB (32); 43 – Boqueirão – PB (32); 44 – Cabaceiras – PB (10;32); 45 – Cacimba de Dentro – PB (32); 46 – Guarabira – PB (32); 47 – Juazeirinho – PB(2); 48 – Soledade – PB (18); 49 – Umbuzeiro – PB (10); 50 – Arcoverde – PE (2;22); 51 – Belo Jardim – PE (2; 23); 52 – Brejo da Madre de Deus – PE (2;23;32;47;49); 53 – Buíque – PE (2; 23); 54 – Caruaru – PE (2;23); 55 – Panelas – PE (23); 56 – Pedra – PE (2); 57 – Sanharó – PE (23); 58 – Toritama – PE (2; 23); 59 – Vertentes – PE (32);60 – Penedo – AL(25;58);61 – Anagé – BA (32); 62 – Aporá – BA (15); 63 – Bom Jesus da Lapa – BA (43); 64 – Contendas do Sincorá – BA (41;42); 65 – Euclides da Cunha – BA (18); 66 – Glória – BA (2); 67 – Irecê – BA (17); 68 – Iuiú – BA (43); 69 – Juazeiro – BA (28,32); 70 – Malhada – BA (43); 71 – Palmas de Monte Alto – BA (43); 72 – Paratinga – BA (43); 73 – São Gonçalo dos Campos – BA (32); 74 – São José – BA (32); 75 – Senhor do Bonfim – BA (14;28); 76- Itacarambi – MG (32;40;56); 77 – Jaíba – MG (33;34;37;56); 78 – Januária – MG (56); 79 – Manga – MG (56); 80 – Mocambinho – MG (32); 81 – São João das Missões – MG (40); 82 – Betânia – PE (4); 83 – Bodocó – PE (2;23); 84 – Floresta – PE (2;4); 85 – Orocó – PE (2;23;51); 86 – Petrolândia – PE (2;23); 87 – Salgueiro – PE (2;23); 88 – São Caetano do Navio – PE (32); 89 – São José do Egito – PE (48); 90 – Serra Talhada – PE(3;2;23;28); 91 – Sertânia – PE (2;23); 92 – Areia Branca – SE (31); 93 – Canindé do São Francisco – SE (1; 2;23); 94 – Itabaiana – SE (29;30;31); 95 – Canarana – BA (44); 96 – Itaeté – BA (16;55); 97 – Iraquara – BA (44); 98- Itaberaba – BA (38); 99 – Gentio do Ouro – BA (32); 100 – Jacobina – BA (32); 101 – João Dourado – BA (44); 102 – Jussiape – BA(38); 103 – Lençóis – BA (38;46); 104 – Morro do Chapéu – BA (32;38;44); 105 – Mucugê – BA (38); 106 – Ourolândia – BA (44); 107 – Palmeiras – BA (44); 108 – Rio de Contas – BA (38); 109 – Utinga – BA (44;45); 110 – Barra – BA (26); 111 – Sobradinho – BA (2); 112 – Pilão Arcado – BA (32); 113 – Canudos – BA (18); 114 – Rodelas – BA (2); 115 – Floresta do Navio – PE (23); 116 – Ibimirim – PE (2;23); 117 – Inajá – PE (23;32); 118 – Jardim – CE (64); 119- São João do Piauí – PI (65). PI, Piauí; CE, Ceará; PB, Paraíba; RN, Rio Grande do Norte; PE, Pernambuco; AL, Alagoas; BA, Bahia; MG, Minas Gerais; SE, Sergipe.
Fig. 6 in Fossil Evidence and the Origin of Bats
Fig. 6. Distribution of Eocene bats in Africa, Australia, and Asia. Note the African record is almost entirely made up of endemic forms and the Old World representation of Eocene bats is poor outside Europe.
Figure 3 in Into the light: atypical diurnal foraging activity of Blyth's horseshoe bat, Rhinolophus lepidus (Chiroptera: Rhinolophidae) on Tioman Island, Malaysia
Figure 3: Spectrogram of echolocation calls of RHiNOlOpHus lepidus recorded at Juara, Tioman Island, on September 26, 2017 at 11:59 h, showing a feeding buzz.
Figure 2 in Into the light: atypical diurnal foraging activity of Blyth's horseshoe bat, Rhinolophus lepidus (Chiroptera: Rhinolophidae) on Tioman Island, Malaysia
Figure 2: IN situ image and characteristic features of the day-flying bats of Tioman Island, Malaysia. (A) Day-flying insectivorous bat flying a low circuit in Paya, Tioman Island, Malaysia. (B and C) Frontal and lateral views of diurnal RHiNOlOpHus lepidus displaying characteristic features of the species, i.e. pointed lancelet with concave sides, triangular connecting process and hair with light tips.
Figure 1 in Summer temperature and precipitation govern bat diversity at northern latitudes in Norway
Figure 1 Predicted values (lines) of finding other species than the northern bat in temperature (A) and precipitation (B) gradients (x-axis) based on the GLM-model. Each tick represents one of the 45 sites where ultrasound loggers were deployed. The figure predicting the effect of temperature is based on a separate GLM-model fit including temperature as a single factor with average precipitation values. The figure presenting precipitation shows predicted values only in the temperature range where variation in diversity was found during this study (from 10 to 12°C).
of central in) KCC (Cave Chakan Khao and) KWC ( Cave] Wongkot Acari and, Khao Dermaptera at 2016, September Isoptera, to 2015 Plecoptera, October Psocoptera during, traps Blattodae, suction Odonata in, collected Trichoptera insects, of Orthoptera mass include dry Percent Others [ .. 2. Thailand ABLE T in The wrinkle-lipped free-tailed bat (Chaerephon plicatus Buchannan, 1800) feeds mainly on brown planthoppers in rice fields of central Thailand
of central in) KCC (Cave Chakan Khao and) KWC ( Cave] Wongkot Acari and, Khao Dermaptera at 2016, September Isoptera, to 2015 Plecoptera, October Psocoptera during, traps Blattodae, suction Odonata in, collected Trichoptera insects, of Orthoptera mass include dry Percent Others [ .. 2. Thailand ABLE T
FIG. 2 in The wrinkle-lipped free-tailed bat (Chaerephon plicatus Buchannan, 1800) feeds mainly on brown planthoppers in rice fields of central Thailand
FIG. 2. Percent volume and percent frequency (0 ± SE) of insect orders found in fecal samples of C. plicatus collected monthly from October 2015 to September 2016 at Khao Wongkot cave (KWC, 70% surrounding rice fields)and Khao Chakan cave (KCC, 22% surrounding rice fields) in central Thailand. [Other: Orthoptera and Hymenoptera combined]
FIG. 2 in How do young bats find suitable swarming and hibernation sites? Assessing the plausibility of the maternal guidance hypothesis using genetic maternity assignment for two European bat species
FIG. 2. Simulation (10,000 iterations) of how often mother-offspring pairs are expected to arrive on the same night by chance for M. daubentonii (top) and M. nattereri (bottom); the observed number of pairs arriving on the same night is denoted by the arrow
FIG. 7 in Terrestrial behavior and trackway morphology of Neotropical bats
FIG. 7. Screen capture outlines of S. bilineata searching behavior: A) Initial position with feet stationary and distal to body; B–C) Bat retracts right pes then extends it distal to body; D–F) Bat plants right pes and retracts then extends left pes; G–H) Left pes planted and bat begins to retract right pes as it leans to right. Screen captures taken approximately 0.125 seconds apart
FIG. 1 in Ecomorphological diversity in the Patagonian assemblage of bats from Argentina
FIG. 1. Localities of study specimens of Patagonian bats from Argentina. Eco-regions from Argentina are coded as follows: Patagonian Steppe (clear gray); Patagonian Forest (dark gray); Low Monte (gray). Histiotus macrotus (∆), H. magellanicus (+), H. montanus (£), L. varius (u), M. chiloensis (ä), and T. brasiliensis (™). Scale in map (black bar) = 100 km
FIG. 7 in Ecomorphological diversity in the Patagonian assemblage of bats from Argentina
FIG. 7. Ordination diagram of PCA of the Patagonian bat assemblage for combined three data sets using A) data set not size-corrected; and B) data set size-corrected. Polygons include specimens from each species: H. macrotus (▲), H. magellanicus (), H. montanus (▲), L. varius (■), M. chiloensis (●), and T. brasiliensis (£). Vectors show the strengh of correlation of each variable with the plane of PC1 and PC2. See text for abbreviations
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.