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183 results for “cave fauna”
FIGURE 7 in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 7. Cave-forming carbonate rocks (gray) of the US and Mexico (modified from Weary and Doctor (2014) and Servicio Geológico Mexicano (2022). Counties (US) and municipalities (MX) where Texoreddellia have been collecte are outlined. The El Sabinal cave (red cross) is located in an isolated carbonate area, surrounded by non-cave forming rocks. It is distant (450 km) from the nearest karstic carbonate areas in western Texas with previously described species of Texoreddellia.
FIGURE 6 in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 6. Number of annuli of gonapophyses by the apex of stylets VIII. All previously described species have only 3.5‒5 annuli at this level. Texoreddellia chihuahuensis n. sp. has 7.5 annuli. The new species appears to have a proportionally a more subdivided ovipositor. Apex of the ovipositor is broken in the T. chihuahuensis, therefore total length and total number of annuli are unknown.
FIGURE 5 in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 5. Gruta el Sabinal (type locality). A) Map of Gruta el Sabinal, showing chamber passage morphology in upper section, followed by an abandoned vadose streamway. B) Entrance to Gruta el Sabinal. C) First chamber. D) Lower vadose passage where the specimen of Texoreddellia chihuahuensis n. sp. was found.
FIGURE 2. Texoreddellia chihuahuensis n in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 2. Texoreddellia chihuahuensis n. sp. Holotype female. A, B) Dorsal and ventral views, respectively. C, D) Head, entire dorsal view and central seta-bearing region, respectively. Body length in A & B = 10.1 mm.
FIGURE 4. Texoreddellia chihuahuensis n in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 4. Texoreddellia chihuahuensis n. sp. A, B) Posterior region. Ovipositor broken after eighth annulus. C, D; Urotergite X.
FIGURE 3. Texoreddellia chihuahuensis n in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 3. Texoreddellia chihuahuensis n. sp. A) Mouth parts. B) Labium. C) Galea and lacinia. D) Maxilla. E) Scales.
FIGURE 1 in Miocene divergence for Texoreddellia? An important component of the cave-adapted fauna of Texas and northern Mexico
FIGURE 1. Bayesian tree showing posterior probabilities at each node, followed by ML bootstrap values, only if>0.8 and 70% respectively. Notice that the new population (red) is the most basal clade of all the Texoreddellia species, followed by T. capitesquameo, from western Texas. This western Texas cave is also geographically the closest to the cave inhabited by the new species in Chihuahua, Mexico. Genus Speleonycta (blue) is used to root the tree.
Figure 3 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 3 Boholina laorsriae sp. nov. female: A habitus, dorsal view B urosome, dorsal view C genital double-somite, ventral view D caudal rami, dorsal view E rostrum, frontal view. Scale bars: 100 μm (A); 50 μm (B−E).
Figure 2 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 2 Geographical location and details of sampling site: A map of Thailand and location of Satun province B sampling location of cave in Satun province (indicated by a star) C topography of area around the hill in which the cave is located D sampling point in cave.
Figure 1 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 1 Distribution of the representatives of the genus Boholina: 1B. crassicephala2B. purgata3B. parapurgata4B. munaensis5B. ganghwaensis6B. laorsriae sp. nov.
Figure 4 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 4 Boholina laorsriae sp. nov. female: A segments 1−12 of antennule B segments 13−21 of antennule C segments 22−24 of antennule D antenna E mandible. Scale bars: 50 μm. Roman numerals on antennule correspond to ancestral segments.
Figure 7 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 7 Boholina laorsriae sp. nov. male: A habitus, dorsal view B: urosome, ventral view C segments 1−12 of antennule D segments 13−19 of antennule E segments 20−22 of antennule. Scale bars: 100 μm (A); 50 μm (B−E). Roman numerals on antennule correspond to ancestral segments.
Figure 1 from: Ferreira RL, Giribet G, Du Preez G, Ventouras O, Janion C, Silva MS (2020) The Wynberg Cave System, the most important site for cave fauna in South Africa at risk. Subterranean Biology 36: 73-81. https://doi.org/10.3897/subtbiol.36.60162
Figure 1 Wynberg Cave System and some troglomorphic taxa: APeripatopsis alba (Onycophora: Peripatopsidae) BSpelaeogriphus lepidops (Spelaeogriphacea: Spelaeogriphidae) CParamelita capensis (Amphipoda: Paramelitidae) DTrichoniscus tabulae (Isopoda: Trichoniscidae) EHarpethrix caeca (Diplopoda: Dalodesmidae) FHahnia sp. (Araneae: Hahniidae) GPurcellia argasiformis (Opiliones: Pettalidae) HSpeleomontia cavernicola (Opiliones: Triaenonychidae) IGymnobisium inukshuk (Pseudoscorpiones: Gymnobisiidae) JJapygidae sp.n (Diplura) KProrhynchus cf. brincki (Platyhelminthes: Prorhynchida). Photographs A, C–E, G, H, J from Rodrigo Ferreira; photographs B, I, K from Gonzalo Giribet; photograph F from Peter Swart.
Figure 2 from: Ferreira RL, Giribet G, Du Preez G, Ventouras O, Janion C, Silva MS (2020) The Wynberg Cave System, the most important site for cave fauna in South Africa at risk. Subterranean Biology 36: 73-81. https://doi.org/10.3897/subtbiol.36.60162
Figure 2 A External landscape surrounding the WCSB one of the entrances of the Wynberg cave C graffiti on the walls of Wynberg cave D Dead bat pending on the cave wall EPurcellia argasiformis with a parasitic mite attached to the first leg. Photographs A, B from Rodrigo Ferreira; photographs C, D from Oresti Ventouras; photograph E from Gonzalo Giribet.
FIG. 4 in The worked bone industry and intrusive fauna associated with the prehistoric cave burials of Abri des Autours (Belgium)
FIG. 4. — Some of the animal bones from the Neolithic collective burial of Abri des Autours: A, inferior left canine of a male suid; B, awl made of a sheep or goat metatarsal; C, E, rods made of red deer antler; D, unmodified fragment of roe deer metatarsal; F, rib of a large bovid fashioned into a point (from left to right: internal, lateral and external views). Scale bar: 5 cm.
FIGURE 20 in The collembolan fauna of Maestrazgo caves (Teruel, Spain) with description of three new species
FIGURE 20. Pygmarrhopalites cantavetulae sp. nov., head chaetatoxy.
Supplementary material 1 from: Deleva S, Ulloa A, Oliveira HFM, Simov N, Didonna F, Chaverri G (2023) Cave-dwelling fauna of Costa Rica: current state of knowledge and future research perspectives. Subterranean Biology 47: 29-62. https://doi.org/10.3897/subtbiol.47.113219
Dataset of cave-dwelling organisms occurring in Costa Rica
Figure 1 in Fauna reported from Batu caves, Selangor, Malaysia: annotated checklist and bibliography.
Figure 1: Collector curves of animal species reported from the Batu caves, cumulative by year.
Supplementary material 1 from: Akmali V, Abedini S, Malekpour Fard Z (2022) Bat fauna and conservation assessment of Kurdistan caves, Iran. Subterranean Biology 42: 79-95. https://doi.org/10.3897/subtbiol.42.73282
Figures S1, S2
Figure 2 from: Akmali V, Abedini S, Malekpour Fard Z (2022) Bat fauna and conservation assessment of Kurdistan caves, Iran. Subterranean Biology 42: 79-95. https://doi.org/10.3897/subtbiol.42.73282
Figure 2 Four caves of Kurdistan with the highest priority for conservation programs: A Karaftu B Kamtaran C Darvish Ouliya D Kouna Sham-Sham.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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
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