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Figure 2 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 2 A Gruna do Vandercir cave B surroundings of Gruna do Vandercir cave with its dry characteristic vegetation (Images A Adriano GambariniB Maria Elina Bichuette).
Figure 1 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 1 Map depicting the known distribution of Pseudochthonius ramalho sp. nov. in Gruna do Vandercir cave, located in Bahia state. The cave belongs to karst area in Jacaré formation, Bambuí group.
Figure 11 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 11 Comparison of morphology among some species of Pseudochthonius from Brazil A Holotype Pseudochthonius ramalho sp. nov. (troglobitic) (LES9601) and left chela (A1) BPseudochthonius strinatii (troglobitic) (LES9391) and pedipalp detail (B1) CPseudochthonius biseriatus (troglobitic) (LES9434) and pedipalp detail (C1) DPseudochthonius sp. (epigean) (LES9629) and pedipalp detail (D1) (Images: A D. M. von Schimonsky; A1–C1 L.B.R Fernandes; D–D1 M. E. Bichuette).
Figure 5 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 5 Pseudochthonius ramalho sp. nov. scanning electron images. Paratype female, habitus A dorsal view B ventral view C zoom in on the anterior margin of the carapace with eye spots denoted with red circle. (Images: Luciana B. R. Fernandes).
Figure 6 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 6 Pseudochthonius ramalho sp. nov. female paratype scanning electron images A detail on the right chelicera of serrula exterior and rallumB detail on the right pedipalp trichobothrium isb and ib, lateral C left pedipalp D detail on the left pedipalp teeth. (Images: L. B. R. Fernandes).
Figure 10 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 10 Morphological differences on the carapace of hypogean and epigean species of Pseudochthonius: eyes (denoted with red circle), and the narrowing of the posterior region of the carapace (marked with dashed line on the sides of the carapace) A hypogean P. ramalho sp. nov. (male) B epigean P. thibaudiC epigean P. arabicus.
Figure 3 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 3 Holotype of Pseudochthonius ramalho sp. nov. in natural habitat, at Gruna do Vandercir cave, Serra do Ramalho, Bahia. (Image: Adriano Gambarini).
Figure 9 from: Assis L, von Schimonsky DM, Bichuette ME (2021) The first troglobitic Pseudochthonius Balzan, 1892 (Pseudoscorpiones, Chthoniidae) from the karst area of Serra do Ramalho, Brazil: a threatened species. Subterranean Biology 40: 109-128. https://doi.org/10.3897/subtbiol.40.77451
Figure 9 Distribution of epigean and hypogean Pseudochthonius species in Brazil, with troglobitic representatives detached.
Subspecies and Distribution. T.p.pictaThomas,1892—NWBorneo. T: p. fuscior Medway, 1965 — E Borneo. in Tupaiidae
Subspecies and Distribution. T.p.pictaThomas,1892—NWBorneo. T: p. fuscior Medway, 1965 — E Borneo.
Fig. 30. Crematogaster acaciae Forel, 1892 in Faunal composition, diversity, and distribution of ants (Hymenoptera: Formicidae) of Dhofar Governorate, Oman, with updated list of the Omani species and remarks on zoogeography
Fig. 30. Crematogaster acaciae Forel, 1892, syntype, worker (CASENT0908494, AntWeb.org (Zach Lieberman)). A. Body in profile. B. Head in full-face view. C. Distribution map.
FIGURES 29–30 in Two new species of cave-dwelling Charinus Simon, 1892 from Brazil (Arachnida: Amblypygi: Charinidae)
FIGURES 29–30. Views from inside the Gruta do Padre cave (habitat of Charinus santanensis sp. n.).
Figure 5 from: Miranda GS, Milleri-Pinto M, Gonçalves-Souza T, Giupponi APL, Scharff N (2016) A new species of Charinus Simon 1892 from Brazil, with notes on behavior (Amblypygi, Charinidae). ZooKeys 621: 15-36. https://doi.org/10.3897/zookeys.621.9980
Figure 5 - Behavioral category frequency for all Charinus ruschii sp. n. individuals in 1440 minutes of observation. Sun icon represents the diurnal period and moon icon the dark period.
Figure 1 from: Miranda GS, Milleri-Pinto M, Gonçalves-Souza T, Giupponi APL, Scharff N (2016) A new species of Charinus Simon 1892 from Brazil, with notes on behavior (Amblypygi, Charinidae). ZooKeys 621: 15-36. https://doi.org/10.3897/zookeys.621.9980
Figure 1 - Habitus and details of Charinus ruschii sp. n. (holotype, MNRJ 9235). A Habitus dorsal B Sternum C Frontal process D Dorsal view of left pedipalp tarsus and claw E Frontal view of left pedipalp tarsus and claw F Dorsal view of left pedipalp G Ventral view of left pedipalp. Scale bars: A, F, G: 1 mm; B, C, D, E: 0.5 mm.
Figure 3 from: Miranda GS, Milleri-Pinto M, Gonçalves-Souza T, Giupponi APL, Scharff N (2016) A new species of Charinus Simon 1892 from Brazil, with notes on behavior (Amblypygi, Charinidae). ZooKeys 621: 15-36. https://doi.org/10.3897/zookeys.621.9980
Figure 3 - Charinus ruschii sp. n. female gonopod and detail of leg I (MNRJ9237). A Dorsal view of the female gonopod B Frontal view of the tip of leg I C Detail of sensitive hair type 1 D Detail of sensitive hair type 2 E Glandular opening close to the tip of the tarsus F Modified claw in the tip of the leg. Abbreviations: br: bristle sensilla; c: club sensilla. Scale bars: B: 100 um; C: 5 um; D, E: 2 um; F: 10 um.
Figure 6 from: Miranda GS, Milleri-Pinto M, Gonçalves-Souza T, Giupponi APL, Scharff N (2016) A new species of Charinus Simon 1892 from Brazil, with notes on behavior (Amblypygi, Charinidae). ZooKeys 621: 15-36. https://doi.org/10.3897/zookeys.621.9980
Figure 6 - Difference between time remaining inside shelters in juveniles (n = 5) and adults (n = 12) amblypygids.
Figure 2 from: Miranda GS, Milleri-Pinto M, Gonçalves-Souza T, Giupponi APL, Scharff N (2016) A new species of Charinus Simon 1892 from Brazil, with notes on behavior (Amblypygi, Charinidae). ZooKeys 621: 15-36. https://doi.org/10.3897/zookeys.621.9980
Figure 2 - Chelicerae (A) and distitibia of leg IV (B) of Charinus ruschii sp. n. (MNRJ 9237 and MNRJ 9235, respectively). Scale bars: 1 mm
Fig 6 from: Ngoute C, Kekeunou S (2017) Redescription and diagnosis of the African genus Gemeneta Karsch, 1892 (Orthoptera: Acrididae: Catantopinae). Journal of Orthoptera Research 27: 161-170. https://doi.org/10.3897/jor.26.19995
Fig 6 - External diagnostic characters of Gemeneta spp. A, B. Fastigium of vertex; C–D. Pronotum lateral view; E–F. External genitalia female; A, C, E. G. terrea and B, D, F. G. opilionoides. Scale bars = 1 mm.
Fig 7 from: Ngoute C, Kekeunou S (2017) Redescription and diagnosis of the African genus Gemeneta Karsch, 1892 (Orthoptera: Acrididae: Catantopinae). Journal of Orthoptera Research 27: 161-170. https://doi.org/10.3897/jor.26.19995
Fig 7 - Ectophallus and endophallus of Gemeneta spp. A, B. Entire phallic complex without epiphallus in lateral view; C, D. Entire phallic complex without epiphallus in dorsal view; E, F. Endophallus in ventral view; G, H. Endophallus in lateral view; I, J. Endophallus in dorsal view; A, C, E, G, I. G. terrea and B, D, F, H, J. G. opilionoides; Apodemes of cingulum (Apd): pair of ectophallic sclerotized structures situated dorsally to endophallus; Valves of cingulum (Cv): pair of valves projecting from the posterior end of the cingulum from the arch of cingulum; they form the upper valves of the aedeagus; Ectophallic sheath (Es): the membrane part of ectophallus covering the ventral aedeagal valves and valves of cingulum, often partially sclerotized; Gonopore processes (Gpr): pair of ventral processes from the aedeagal valves, functioning as a pinch valve between the ejaculatory and spermatophore sacs; Ventral aedeagal valves (Vv): endophallic valves, divided in two parts; Zygoma (Zyg): transverse dorsal part of cingulum, connecting the apodemes. Scale bars = 0.5 mm.
Fig 8 from: Ngoute C, Kekeunou S (2017) Redescription and diagnosis of the African genus Gemeneta Karsch, 1892 (Orthoptera: Acrididae: Catantopinae). Journal of Orthoptera Research 27: 161-170. https://doi.org/10.3897/jor.26.19995
Fig 8 - Ectophallus, epiphallus, spermatheca and subgenital plate of Gemeneta spp. A, B. Ectophallus in ventral view; C, D. Epiphallus in axial view; E, F: Epiphallus in lateral view; G, H. Epiphallus in dorsal view; I. Spermatheca in dorsal view; J. Subgenital plate in lateral view; K. Subgenital plate in dorsal view; A, C, E, G, I, J, K. G. terrea and B, D, F, H. G. opilionoides; Ancorae (A): a pair of processes or projections from the anterior margin or the dorsal surface of the epiphallus; Bridge (B): transverse part of epiphallus connecting the lateral parts; Lophi (L): lobiform processes near the posterior margin of the epiphallus; Columella (C): columnar structures on either side of the egg-guide in the subgenital plate; Egg-guide (Eg): median, dorsally produced part of the posterior edge in the subgenital plate; Floor pouches (Fp): pair of short anterior invaginations in the floor of the subgenital plate; Preapical appendix (Pa): preapical dilatation of the spermathecal duct; Posterior edge (Pe): pair of short posterior invaginations of the border that meets the floor in the subgenital plate. Scale bars = 0.5 mm.
Fig. 2 in Ancyrophora gracilis L , 1892 and Actinocephalus permagnus Wellmer, 1910 (Eugregarinorida: Apicomplexa) in natural populations of ground beetles (Coleoptera, Carabidae) - hosts preferences, intensity and seasonal dynamic
Fig. 2. Mean density of Actinocephalus permagnus (AT) and Ancyrophora gracilis (AC) in relation to habitat. Circle – woodland, square – meadow, triangle – arable land
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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
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.