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Figure 9 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis
Figure 9. Echinopsyllus nogueirae sp. nov., female. A, A2; B, P5 with P6. Scale bar = 50 Mm.
Figure 1 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis
Figure 1. Map of Campos Basin showing the sampling stations (modified from Botelho et al. 2007).
Figure 11 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis
Figure 11. Echinopsyllus nogueirae sp. nov., female. A, P3; B, P4. Scale bar = 50 Mm.
Data from: PER-SIMPER - a new tool for inferring community assembly processes from taxon occurrences
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FIGURE 3 in Apennocoris pilosulus: rediscovery of a forgotten big-eyed bug taxon from New Caledonia (Heteroptera: Lygaeoidea: Geocoridae)
FIGURE 3. Details of Apennocoris pilosulus, macropterous male: A. labial trough, B. metapleurite with structures of metathoracic scent efferent apparatus (indicated with red arrow), C. detail of thorax and abdomen in lateral view with dorsal setosity. (scale bar: 1 mm).
FIGURE 2. Apennocoris pilosulus Montandon, 1907 in Apennocoris pilosulus: rediscovery of a forgotten big-eyed bug taxon from New Caledonia (Heteroptera: Lygaeoidea: Geocoridae)
FIGURE 2. Apennocoris pilosulus Montandon, 1907, macropterous male (MNHN): A. dorsal habitus, B. lateral view (scale bar: 1 mm).
FIGURE 1. Apennocoris pilosulus Montandon, 1907 in Apennocoris pilosulus: rediscovery of a forgotten big-eyed bug taxon from New Caledonia (Heteroptera: Lygaeoidea: Geocoridae)
FIGURE 1. Apennocoris pilosulus Montandon, 1907, coleopterous female (lectotype, KNHM): A. dorsal habitus, B. lateral view, C. labels (scale bar: 1 mm).
FIGURE 4. Stylogeocoris biroi Montandon, 1913 in Apennocoris pilosulus: rediscovery of a forgotten big-eyed bug taxon from New Caledonia (Heteroptera: Lygaeoidea: Geocoridae)
FIGURE 4. Stylogeocoris biroi Montandon, 1913 (lectotype, HNHM): A. dorsal habitus, B. labels, C. Thoracic pleurites, with metathoracic scent efferent apparatus (indicated with red arrow) (scale bar: 1 mm).
Data from: A new taxon of cistecephalid dicynodont from the upper Permian Kundaram Formation of India
A new cistecephalid dicynodont, Sauroscaptor tharavati gen. et sp. nov., is described from the upper Permian Kundaram Formation of India. This taxon is represented by specimens formerly referred to the African dicynodont genera Cistecephalus and Emydops. Sauroscaptor can be distinguished from other cistecephalids by the extremely posterior position of the pineal foramen (overhanging the edge of the occiput), bipartite nuchal crest, and relatively narrow skull roof. The recognition of Sauroscaptor as a distinct cistecephalid taxon adds to the increasing evidence for high levels of basinal endemism in this family. However, dicynodont biogeographical patterns are complex, and there is no simple relationship between inferred dispersal ability based on body size and levels of endemicity within clades.
Data from: Extensive yellow crusts below limestone overhangs: a new taxon close to a minute epiphytic lichen
A conspicuous yellow crust forming extensive covers on some dry and shaded limestone rocks in Europe is described here as Caloplaca substerilis subsp. orbicularis M. Haji Moniri, Vondrák & Malíček subsp. nov. Based on nuITS rDNA, 28S nuLSU rDNA and mtSSU rDNA sequence data, the new taxon is closely related to Caloplaca sterilis and C. ulcerosa. The three taxa form a supported clade in the subfamily Xanthorioideae (Teloschistaceae), but none of the recent genera are suitable for them. In the ITS phylogeny, the new taxon forms a monophylum nested within C. substerilis. Its extensive yellow thalli and absence of vegetative diaspores clearly distinguish it from Caloplaca substerilis (subsp. substerilis). Indeed, if it had not been for the molecular evidence, we would have described it at the rank of species. We suggest that the substrate switch and accompanying processes are responsible for the striking phenotype difference between Caloplaca substerilis subsp. substerilis and C. substerilis subsp. orbicularis.
FIGURE 3. Maximum parsimony phylogenetic relationships with the taxon Pituna poranga removed. Heuristic search with 50 in Description of a new annual rivulid killifish genus from Venezuela
FIGURE 3. Maximum parsimony phylogenetic relationships with the taxon Pituna poranga removed. Heuristic search with 50 random additions and TBR branch swapping resulted in a single most parsimonious topology of 5706 steps. Numbers above nodes are bootstrap values based on 2000 pseudoreplicates (25 random additions each); only values over 50 are reported. Numbers below branches are Bremer support indices which are equivalent to unreversed synapomorphies.
FIGURE 3 in Thalasseleotrididae, new family of marine gobioid fishes from New Zealand and temperate Australia, with a revised definition of its sister taxon, the Gobiidae (Teleostei: Acanthomorpha)
FIGURE 3. Lower part of left side first branchial arch and hyoid arch in dorsal view showing degree of development of gill membrane (white) in: A) the odontobutid Micropercops swinhonis, same specimen as in Fig. 1; B) the thalasseleotridid Grahamichthys radiatus, same specimen as in Fig. 1. Abbreviations: ACH, anterior ceratohyal; CB1, ceratobranchial 1; DHH, dorsal hypohyal; GM, gill membrane; HB1, hypobranchial 1; PCH, posterior ceratohyal; VHH, ventral hypohyal. Gill rakers not illustrated. Scale bars = 1 mm.
FIGURE 1 in Thalasseleotrididae, new family of marine gobioid fishes from New Zealand and temperate Australia, with a revised definition of its sister taxon, the Gobiidae (Teleostei: Acanthomorpha)
FIGURE 1. Ventral view of right ceratobranchial 5 of: A) the odontobutid Micropercops swinhonis (Günther), AMS I.27275, 42 mm SL; B) the thalasseleotridid Grahamichthys radiatus, AMS I.41350-001, 51.8 mm SL; C) the thalasseleotridid Thalasseleotris adela, AMS I.18241-035, 27.1 mm SL; D) the gobiine gobiid Lophogobius cyprinoides (Pallas), AMS uncat., 41 mm SL. Arrow in D points to ventral process; scale bars = 0.5 mm.
FIGURE 6 in Thalasseleotrididae, new family of marine gobioid fishes from New Zealand and temperate Australia, with a revised definition of its sister taxon, the Gobiidae (Teleostei: Acanthomorpha)
FIGURE 6. Dorsal view of left dorsal gill arches of: A) the odontobutid Perccottus glenii, same specimen as in Fig. 2; B) the thalasseleotridid Grahamichthys radiatus, same specimen as in Fig. 1; C) the thalasseleotridid Thalasseleotris adela, same specimen as in Fig. 1; D) the gobiine gobiid Callogobius maculipinnis (Fowler), MPM 45773, 31.6 mm SL. Abbreviations: IAC – interarcual cartilage; EB1–4, epibranchials 1–4; PB1–3, pharyngobranchials 1–3; PB4C, pharyngobranchial 4 cartilage; PB4TP, pharyngobranchial 4 toothplate. Gill rakers not illustrated. Scale bars = 0.5 mm.
FIGURE 5 in Thalasseleotrididae, new family of marine gobioid fishes from New Zealand and temperate Australia, with a revised definition of its sister taxon, the Gobiidae (Teleostei: Acanthomorpha)
FIGURE 5. Lateral view of left posterior ceratohyal and interhyal, and dorsal view of posterior ceratohyal with interhyal removed of: A) the odontobutid Perccottus glenii; B) the eleotridid Gobiomorus dormitor; C) the eleotridid Eleotris melanosoma; D) the eleotridid Dormitator latrifrons; E) the thalasseleotridid Thalasseleotris adela; F) the thalasseleotridid Grahamichthys radiata; G) the gobiine gobiid Gobius niger; H) the gobionelline gobiid Stenogobius zurstrasseni; I) the gobiine gobiid Valenciennea sexguttata. All specimens as in Fig. 4. Scale bars = 1 mm. AC, anterior ceratohyal; PC, posterior ceratohyal; IH, interhyal.
FIGURE 4 in Thalasseleotrididae, new family of marine gobioid fishes from New Zealand and temperate Australia, with a revised definition of its sister taxon, the Gobiidae (Teleostei: Acanthomorpha)
FIGURE 4. Lateral (left) and dorso-lateral (right) views of left interhyal of: A) the odontobutid Perccottus glenii, same specimen as in Fig. 2; B) the eleotridid Gobiomorus dormitor, same specimen as in Fig. 2; C) the eleotridid Eleotris melanosoma, same specimen as in Fig. 2; D) the eleotridid Dormitator latrifrons (Richardson), ANSP 140703, 53.1 mm SL; E) the thalasseleotridid Thalasseleotris adela, same specimen as in Fig. 2; F) the thalasseleotridid Grahamichthys radiata, same specimen as in Fig. 2; G) the gobiine gobiid Gobius niger, same specimen as in Fig. 2; H) the gobionelline gobiid Stenogobius zurstrasseni (Popta), USNM 264770, 45.9 mm SL (right side reversed); I) the gobiine gobiid Valenciennea sexguttata (Valenciennes in Cuvier & Valenciennes), MPM 43110, 55.5 mm SL. Arrows in E–I indicate cup-shaped process. Scale bars = 0.5 mm.
FIGURE 14 in Taxonomic circumscription of Adenomera martinezi (Bokermann, 1956) (Anura: Leptodactylidae: Leptodactylinae) with the recognition of a new cryptic taxon through a bioacoustic approach
FIGURE 14. Geographic distribution of Adenomera martinezi and Adenomera saci sp. nov. on a topographic map. Type localities: Circle—A. martinezi (Cachimbo, Pará); Square—Adenomera saci sp. nov. (Chapada dos Veadeiros, Goiás). Triangles correspond to the distributional records for Adenomera saci sp. nov.: (1) Sonora, State of Mato Grosso do Sul; (2) Alto Araguaia, (3) Pontal do Araguaia, (4) Ribeirão Cascalheira, and (5) Santa Terezinha, State of Mato Grosso; (6) Mineiros/ Chapadão do Céu, (7) Cristalina, (8) Brasília, (9) Niquelândia, (10) Minaçu, and (11) Buritinópolis, State of Goiás/Distrito Federal; (12) Formoso do Araguaia/Ilha do Bananal, (13) Almas, and (14) Rio da Conceição/Jalapão, State of Tocantins. Records were based on our data and extracted from Heyer (1973); Vitt et al. (2005); Cintra et al. (2009); Moreira et al. (2009); Oda et al. (2009); Silva Jr. et al. (2009); Kopp et al. (2010); Morais et al. (2011); Valdujo et al. (2012).
FIGURE 13 in Taxonomic circumscription of Adenomera martinezi (Bokermann, 1956) (Anura: Leptodactylidae: Leptodactylinae) with the recognition of a new cryptic taxon through a bioacoustic approach
FIGURE 13. Lateral (A) and dorsal (B) views, and schematic diagram of the oral disc (C) of a tadpole (stage 37) of Adenomera saci sp. nov. from Cristalina, State of Goiás.
FIGURE 5 in Taxonomic circumscription of Adenomera martinezi (Bokermann, 1956) (Anura: Leptodactylidae: Leptodactylinae) with the recognition of a new cryptic taxon through a bioacoustic approach
FIGURE 5. Live adult male specimens of Adenomera saci sp. nov. from the type locality (Chapada dos Veadeiros, Goiás): (A) Holotype AAG-UFU 1339 (SVL 22.5 mm); (B) Voucher paratopotype AAG-UFU 0109 (SVL 22.5 mm); (C) Paratopotype AAG-UFU 0108 (SVL 20.1 mm); (D) Paratopotype AAG-UFU 0762 (SVL 20.5 mm); (E) Paratopotype AAG-UFU 0763 (SVL 22.0 mm).
FIGURE 9 in Taxonomic circumscription of Adenomera martinezi (Bokermann, 1956) (Anura: Leptodactylidae: Leptodactylinae) with the recognition of a new cryptic taxon through a bioacoustic approach
FIGURE 9. Advertisement call of two male specimens of Adenomera saci sp. nov. from the type locality. (A) A waveform section (2 seconds) with five calls from the Parque Nacional da Chapada dos Veadeiros (Goiás); (B) Audiospectrogram (above) and respective oscillogram (below) of the third call highlighted by a red outline. Unvouchered recording. (C) A waveform section (2.5 seconds) with five calls from Alto Paraíso de Goiás (Goiás); (D) Audiospectrogram (above) and respective oscillogram (below) of the third call highlighted by a red outline. Voucher paratopotype: AAG-UFU 0109.
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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.