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FIGURE 3 in A new, narrowly distributed, and critically endangered species of Characidium (Characiformes: Crenuchidae) from the Distrito Federal, Central Brazil
FIGURE 3 | Osteological characteristics in Characidium onca, paratypes: A. Right upper jaw in medial view (MZUSP 125803); B. Right dentary in medial view (MZUSP 125803); C. Left pectoral gridle in lateral view (MZUSP 125801); D. Skull in dorsal view (MZUSP 125803); E. Posterior portion of skull in dorsal view (MZUSP 125801). Abbreviations: ANT, antorbital; CLE, cleithrum; COR, coracoid; DEN, dentary; dentl, lateral row of dentary teeth; dentm; middle row of dentary teeth; dentr, replacement lateral row of dentary teeth; DPSO, dorsal process of the supraoccipital; ESC, extrascapular; FR, frontal; fbsc, frontal branch of the supraorbital canal; fo, fontanel; IO 1–6, infraorbitals 1 to 6; MCO, mesocoracoid; MEC, Meckel's cartilage; METH, mesethmoid; MX, maxilla; NA, nasal; PAR, parietal; pbsc, parietal branch of the supraorbital canal; PCP, posterior cleithral process; PCL 1–3, postcleithrum 1 to 3; PMX, premaxilla; pmxt, premaxilarry teeth; pmxtr, replacement premaxillary teeth; POST, posttemporal; PTE, pterotic; SC, scapula; SCL, supracleithum; SUO, supraorbital. Scale bar = 1 mm.
FIGURE 2 in A new, narrowly distributed, and critically endangered species of Characidium (Characiformes: Crenuchidae) from the Distrito Federal, Central Brazil
FIGURE 2 | Paratypes of Characidium onca. A–B. MZUSP 125798, 23.8–27.0 mm SL respectively, córrego Taquara; C. MZUSP 125795, 28.6 mm SL, córrego Roncador; D. ZUEC 17242, 38.7 mm SL, córrego Roncador; E–F. MZUSP 125797, 39.0–44.1 mm SL, respectively, córrego Roncador. Scale bar = 5 mm.
Figure 2 in The westernmost occurrence of Gnathorhiza in the Triassic, with a discussion of the stratigraphic and palaeogeographic distribution of the genus
Figure 2. Palaeobiogeography of Gnathorhiza during Carboniferous and Permian (a) and Triassic (b). 1, Gnathorhiza sp.: USA, southeastern Utah, Cutler Group, Halgaito Formation (Vaughn, 1966, 1969, 1973); 2, Gnathorhiza sp.: USA, New Mexico, Rio Arriba County, Cutler Group (Berman, 1993); 3, G. bothrotreta: USA, New Mexico, Socorro County, Valencia County, Abo Formation (Berman, 1976, 1993), Gnathorhiza sp.: USA, New Mexico, Sandoval County, Abo Formation, San Miguel County, Sangre de Cristo Formation (Berman and Reisz, 1980); 4, Gnathorhiza sp.: USA, Arizona, Cochise County, Black Prince Limestone (Thayer, 1985); 5, G. serrata: USA, Texas, Baylor County, Lauders Formation and Wilbarger County, Arroyo Formation (Cope, 1883; Dalquest, 1968; Dalquest et al., 1989), G. dikeloda: Knox County, Vale and Choza Formation (Olson, 1951), Gnathorhiza sp.: north-central Texas, Nocona, Petrolla, Waggoner ranch Formations (Johnson and May, 2013); 6, G. pusilla: USA, Oklahoma, Grant County, Garber Formation (Case, 1915), G. serrata: Noble County, Wellington Formation (Carlson, 1968), Cleveland County, Hennessey Formation, G. noblensis (Olson, 1970; Olson and Daly, 1972); 7, Gnathorhiza sp.: USA, Kansas, Geary County, Lyon County, Speiser Shale (Schultze, 1985), Brown County, Bern Limestone Formation (Chorn and Schultze, 1990), Greenwood County, Hamilton Quarry (Cunnigham, 1993), Key County, Matfield Formation (McCahon and Miller, 2015); 8, G. serrata, G. dikeloda: USA, Nebraska, Richardson County, Eskridge Formation (Huttenlocker et al., 2005, 2013); 9, G. pusilla: USA, Illinois, Vermillion County (Cope, 1877); 10, aff. Gnathorhiza: Germany, Saar–Nahe Basin (Boy and Schindler, 2000; Schindler, 2007); 11, G. tatarica, G. otschevi: Russia, Orenburg region, Kutulukskaya Svita (Minikh, 1989, 1992), Gnathorhiza sp.: Kulchumovskaya Svita (Tverdokhlebov et al., 2005); 12, Gnathorhiza sp.: Brazil, Sao Paulo State, Corumbatai Formation, Paraná State, Rio do Rasto Formation (Toledo and Bertini, 2005); 13 Gnathorhiza sp.: Brazil, Rio Grande do Sul State, Rio do Rasto Formation (Ragonha, 1989; Richter and Langer, 1998); 14, Gnathorhiza sp.: Oman, Al Wusta region, Gharif Formation (Schultze et al., 2008); 15, Gnathorhiza otschevi: Poland, Czatkowice 1, karst fillings (this paper); 16, G. triassica triassica, G. triassica baskunchakensis, G. triassica beresnikiensis: Russia, Arkhangelsk Oblast (Minikh, 1977); 17, G. triassica triassica: Russia, Komi Republic (Minikh, 1977); 18, G. triassica triassica, G. triassica baskunchakensis: Russia, Kirov Oblast (Minikh, 1977); 19, G. triassica triassica, G. triassica beresnikiensis, G. lozovskii, G. bogdensis: Russia, Vologda Oblast (Minikh, 1977); 20, G. otschevi, G. triassica triassica, G. triassica beresnikiensis, G. bogdensis: Russia, Kostroma Oblast (Minikh, 1977); 21, G. triassica triassica, G. lozovskii: Russia, Yaroslavl Oblast (Minikh, 1977; Novikov and Sennikov, 1997); 22, Gnathorhiza otschevi: Russia, Vladimir Oblast (Newell et al., 2010); 23, G. triassica triassica: Russia, Nizhny Novgorod Oblast (Minikh, 1977, 2000); 24, G. otschevi, G. triassica triassica, G. triassica beresnikiensis, G. triassica baskunchakensis, G. lozovskii: Russia, Orenburg Oblast (Minikh, 1977; Minikh and Minikh, 1997); 25, G. triassica triassica, G. triassica baskunchakensis: Kazakhstan, Atyrau Oblast (Minikh and Minikh, 1997); 26, G. otschevi, G. triassica baskunchakensis, G. bogdensis: Russia, Bolshoye Bogdo Mountain (Minikh, 1977; Minikh and Minikh, 1997). Numbers not in stratigraphic order. Lower Permian and Early Triassic palaeogeographic maps modified from http://cpgeosystems.com/paleomaps.html.
Figure 1 in The westernmost occurrence of Gnathorhiza in the Triassic, with a discussion of the stratigraphic and palaeogeographic distribution of the genus
Figure 1. Tooth plates of Gnathorhiza otschevi from Czatkowice 1. (a, b) Upper tooth plate, ZPAL P. VII/6 in occlusal view and (c) in lateral view, and (d) a section of the first ridge; (e, f) lower tooth plate, ZPAL P. VII/7, in occlusal view and in dorsal view (g); (h) lower tooth plate, ZPAL P. VII/9, in occlusal view and (i) in medial view; (j) upper tooth plate, ZPAL P. VII/5, in occlusal view; (k) measurements of Minikh (1977) method. Scale bar for (a)–(c) and (e)–(j) 1 mm, 0.5 mm for (d).
Figure 3 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
Figure 3. Bivariate plot of the examined samples of the Myotis mystacinus morphogroup from the Caucasus region: tibia length (LTib) against the thumb length (LPol). For explanations see Figure 2.
Figure 6 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
Figure 6. Bivariate plot of the examined samples of the Myotis mystacinus morphogroup from the Caucasus region: results of the principal component analysis of the dimensions and relative dimensions of upper canines and premolars. For explanations see Figure 2.
Figure 2 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
Figure 2. Bivariate plot of the examined samples of the Myotis mystacinus morphogroup from the Caucasus region: greatest length of skull (LCr) against the length of the upper tooth-row (CM3). The closed symbols denote specimens identified with the help of genetic analysis (with the exception of M. brandtii, for details see text), open symbols all other specimens (arranged to geographical sets); bold capital letters denote holotype specimens of the following taxa: A – Myotis mystacinus aurascens Kuzâkin, 1935; C – Myotis mystacinus caucasicus Tsytsulina, 2000; M – Myotis meinertzhageni Thomas, 1926; P – Myotis mystacinus popovi Strelkov, 1983; R – Myotis mystacinus pamirensis Kuzâkin, 1935; S – Myotis mystacinus sogdianus Kuzâkin, 1934; T – Myotis mystacinus transcaspicus Ogneff & Heptner, 1928.
Figure 5 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
Figure 5. Bivariate plot of the examined samples of the Myotis mystacinus morphogroup from the Caucasus region: results of the principal component analysis of all tooth dimensions and relative dimensions. For explanations see Figure 2.
Figure 4 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
Figure 4. Bivariate plot of the examined samples of the Myotis mystacinus morphogroup from the Caucasus region: results of the principal component analysis of all skull dimensions and relative dimensions. For explanations see Figure 2.
Figure 1. Bayesian 50 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
Figure 1. Bayesian 50% majority rule consensus tree depicting the phylogenetic relationships in the Myotis mystacinus morphogroup from the Caucasus region and adjacent parts of the Western Palaearctic based on the cytochrome b sequences.
Figure 8 in Distribution and molecular differentiation of Culex pipiens complex species in the Middle and Eastern Black Sea Regions of Turkey
Figure 8. Unrooted haplotype network for CQ11. Each circle represents a haplotype, and lines above each link indicate mutations.
Figure 7 in Distribution and molecular differentiation of Culex pipiens complex species in the Middle and Eastern Black Sea Regions of Turkey
Figure 7. Phylogenetic tree based on a 151-bp region within the CQ11 microsatellite region of Culex pipiens. The tree was constructed using the maximum likelihood method, and bootstrap values are shown as numbers on the tree.
Figure 5. Unrooted haplotype network. Each circle represents a in Distribution and molecular differentiation of Culex pipiens complex species in the Middle and Eastern Black Sea Regions of Turkey
Figure 5. Unrooted haplotype network. Each circle represents a haplotype, and the lines above each link indicate one mutation. Small black dots indicate intermediate, missing, or unsampled haplotypes.
Figure 4 in Distribution and molecular differentiation of Culex pipiens complex species in the Middle and Eastern Black Sea Regions of Turkey
Figure 4. The phylogenetic tree is based on a 651-bp region of the Ace-2 gene from Culex pipiens. The tree was constructed using the maximum likelihood method, and bootstrap values are shown as numbers on the tree.
F I G U R E 3 in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 3 Images of the proximal and distal sides of the right and left otoliths from black ruff Centrolophus niger (Gmelin, 1789). Scale bar and the plane at which the length and width of the otolith were measured are shown.
F I G U R E 1 in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 1 Three specimens of black fish (Centrolophus niger) caught during the International Ecosystem Summer Survey of the Nordic Seas in 2021. Specimens were photographed prior to freezing. Photograph by James Kennedy.
F I G U R E 8 Total length v in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 8 Total length v. (a) total weight, (b) fork length, and (c) standard length for black ruff Centrolophus niger (Gmelin, 1789) from the current and previous studies. The origin of the previous data is indicated in the legend. (a) Nonlinear and (b, c) linear regression models are shown. Note that total weight corresponds to frozen weight for measurements in the current study, whereas for previous studies, corresponds to the weight given in the respective study.
F I G U R E 2 in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 2 Location of sampling stations of the Icelandic component of the International Ecosystem Summer Survey of the Nordic Seas 2009–2021. Stations where black ruff Centrolophus niger (Gmelin, 1789) were caught are shown in Black. The main surface currents in the Northeast Atlantic are shown in the final panel; the cold East Greenland current (green) and the warm Atlantic current (red) (Blindheim & Østerhus, 2005).
F I G U R E 7 Total length v in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 7 Total length v. (a) frozen weight, (b) fork length, (c) and standard length and frozen weight v. (d) thawed weight for black ruff Centrolophus niger (Gmelin, 1789). (a) Nonlinear and (b–d) linear regression models are shown (a–d) as well as x = y line (d).
F I G U R E 4 in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 4 Temperature profiles from the CTD probe at each station of the Icelandic part of the International Ecosystem Summer Survey of the Nordic Seas (IESSNS) where black ruff Centrolophus niger (Gmelin, 1789) were caught.
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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.