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FIG. 38 in Ascidians from the tropical western Pacific
FIG. 38. — Larva; A, Polycitor giganteus (Herdman, 1899); B, Polycitor translucidus Kott, 1957. Scale bars: 0.5 mm.
FIG. 21 in Ascidians from the tropical western Pacific
FIG. 21. — Synoicum castellatum Kott, 1992; A, B, two parts of a zooid; C, thorax and abdomen. Scale bar: A, B, 2 mm; C, 1 mm.
FIG. 30 in Ascidians from the tropical western Pacific
FIG. 30. — Eudistoma gracilum Kott, 1990; A, zooid; B, other side of the abdomen; C, larva. Scale bars: A, B, 1 mm; C, 0.25 mm.
FIG. 26. — Cystodytes hapu Monniot C. & Monniot F., 1987 in Ascidians from the tropical western Pacific
FIG. 26. — Cystodytes hapu Monniot C. & Monniot F., 1987; A, B, zooid in two parts; C, incubating zooid; D, right side of the larva; E, anterior part of the left side of the larva. Scale bars: A, B, D, E, 0.5 mm; C, 1 mm.
FIG. 25. — Clavelina maculata n in Ascidians from the tropical western Pacific
FIG. 25. — Clavelina maculata n. sp.; A, B, both sides of a zooid; C, thorax; D, larva. Scale bars: A-C, 2 mm; D, 0.5 mm.
FIG. 13. — Aplidium vulcanium n in Ascidians from the tropical western Pacific
FIG. 13. — Aplidium vulcanium n. sp.; A, B, two parts of the same zooid; C, thorax; D, abdomen; E, F, ovaries; G, part of the branchial sac. Scale bars: A-C, E-G, 1 mm; D, 0.5 mm.
FIG. 34 in Ascidians from the tropical western Pacific
FIG. 34. — Eudistoma tumidum Kott, 1990; A, zooid; B, base of the abdomen; C, larva. Scale bars: A, B, 1 mm; C, 0.25 mm.
FIG. 20 in Ascidians from the tropical western Pacific
FIG. 20. — Pseudodistoma novaezelandiae (Brewin, 1950); A, B, two parts of a zooid; C, D, abdomen; E, larva. Scale bars: A-D, 1 mm; E, 0.5 mm.
FIG. 31. — Eudistoma inauratum n in Ascidians from the tropical western Pacific
FIG. 31. — Eudistoma inauratum n. sp.; A, B, two parts of a zooid; C, larva. Scale bars: A, B, 1 mm; C, 0.5 mm.
FIG. 1. — Tetracanthella bichaeta n in Three new species of Tetracanthella (Collembola, Isotomidae) from western Europe
FIG. 1. — Tetracanthella bichaeta n. sp.; A, ocelli and PAO; B, distal part of Tita I; C, chaetotaxy of Tita III in adult male; D, furcal area; E, dorsal chaetotaxy of Th. II; F, dorsal chaetotaxy of Abd. II-VI; G, dorsal plates in axial area near p1-chaetae of Abd. IV. In E and F, axial chaetae are marked. Abbreviations: Abd. II-VI, abdominal tergites II-VI; PAO, postantennal organ; Th. II, thoracic tergite II; Tita
FIG. 3. — A-E, Tetracanthella fusca n in Three new species of Tetracanthella (Collembola, Isotomidae) from western Europe
FIG. 3. — A-E, Tetracanthella fusca n. sp.; A, ocelli (pars) and PAO; B, dorsal chaetotaxy of Abd. II-VI; C, furcal area; D, dorsal plates in axial area near p1-chaetae of Abd. IV; E, chaetotaxy of Tita III; F, T. similis Deharveng, 1987, dorsal chaetotaxy of Abd. III-IV. In B and F, axial chaetae and s-chaetae are marked. Abbreviations: Abd. II-VI, abdominal tergites II-VI; PAO, postantennal organ; Tita III,
FIG. 2. — Tetracanthella corsica n in Three new species of Tetracanthella (Collembola, Isotomidae) from western Europe
FIG. 2. — Tetracanthella corsica n. sp.; A, ocelli and PAO; B, furcal area; C, chaetotaxy of Tita III in adult male; D, dorsal chaetotaxy of tergites and posterior edge of head; E, dorsal plates of Abd. V-VI. In D, axial chaetae are marked (only left side on Th. II-III). Abbreviations: Abd. V-VI, abdominal tergites V-VI; PAO, postantennal organ; Th. II, III, thoracic tergite II, III; Tita III, tibiotarsus III.
Text-fig. 1. Map of the Carboniferous-Permian non-marine basins of the Czech Republic; the star indicates roughly the position of the locality Ploužnice in the north-western part of the Krkonoše Piedmont Basin (according to Opluštil et al. 2016b). in Fossil Fauna And Flora Of A Re-Discovered Locality In The Late Carboniferous Ploužnice Horizon Of The Krkonoše Piedmont Basin, Bohemian Massif
Text-fig. 1. Map of the Carboniferous-Permian non-marine basins of the Czech Republic; the star indicates roughly the position of the locality Ploužnice in the north-western part of the Krkonoše Piedmont Basin (according to Opluštil et al. 2016b).
Fig. 11 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 11. Topographic map of Antelope Pass, Hidalgo County New Mexico showing the 23 trap sites listed in table 6. Each site can be identified by its coordinates and symbol (table 6). Triangles indicate sites where A. dixoni C was found, but not A. t. punctilinealis; squares indicate sites where A. t. punctilinealis was found, but not A. dixoni C; and dots indicate sites where both species were found. This was mapped with TOPO! (2003, National Geographic; www.nationalgeographic.com/topo).
Fig. 7 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 7. Pattern of morphological variation expressed by the distribution of scores on the first two principal components extracted from a correlation matrix of seven meristic characters of 30 specimens of Aspidoscelis from Antelope Pass, Hidalgo County, New Mexico. The specimens include representatives of two species (A. dixoni C and A. t. punctilinealis) and hybrids between them. Note that the three hybrids cluster most closely to their maternal parent.
Fig. 5 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 5. Karyotypes of two whiptail lizards (Aspidoscelis) from Antelope Pass, Peloncillo Mountains, Hidalgo County, New Mexico. A, Diploid unisexual A. dixoni C (AMNH R-148360, fig. 3), with 2n 5 46 chromosomes. This taxon is a clone with its ultimate ancestor having been an F1 hybrid between A. tigris marmorata (haploid complement of chromosomes in the upper two rows) X A. gularis septemvittata (haploid complement in the lower two rows of A). Note that the X chromosome that was ultimately inherited from marmorata (third largest, upper row) was apparently fissioned at the centromere (arrow) forming two additional set II-sized macrochromosomes (here arranged to suggest the ancestral unfissioned state in marmorata). Note also that the missing microchromosome of A. dixoni C is illustrated as missing from the marmorata genome (o at the right end of the second row), although we do not know from which genome it was actually lost. B, Triploid hybrid female of A. dixoni C X A. t. punctilinealis (AMNH R-148141, fig. 3), with 3n 5 69 chromosomes arranged in six rows. Rows 2 and 4 represent the haploid complement most recently inherited from A. t. punctilinealis, including its intact X chromosome (third largest). Rows 1, 3, 5, and 6 represent the two haploid complements inherited from A. dixoni C, including the fissioned X (arrow) chromosome and missing microchromosome (o), as in A, above. Bar represents 10 Mm.
Fig. 6 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 6. Electrophoretic phenotypes representing products of four gene loci of Aspidoscelis. A, IDDH, a tetrameric enzyme, from liver homogenates of seven lizards. Note that the b-allele from PUN is very faint but present in the hybrid. B, PEPA, a dimeric enzyme, from muscle homogenates of seven lizards. Note that New Mexican dixoni differ from Texan dixoni and that the hybrid is triallelic. C, sMDH, a dimeric enzyme, from muscle homogenates of seven lizards. Note that New Mexican dixoni differ from Texan dixoni and the hybrid shows two doses of the a-allele. D, MPI, a monomeric enzyme, from muscle homogenates of eight lizards. Note that New Mexican dixoni differ from Texan dixoni. Letters below gels identify allozymes based on alleles present (table 2). Lanes for individual lizards are labeled beside the gel (with genotype) as follows: DIXA, A. dixoni A; DIXB, A. dixoni B; DIXC, A. dixoni C; DIXC X PUN, hybrid of A. dixoni C X A. t. punctilinealis; MAR, A. t. marmorata; SCA, A. g. scalaris, which at these loci are often the same as A. g. septemvittata; TESC, A. tesselata C-E; TESD, A. tesselata D; TESE-C, A. tesselata E-C; PUN, A. t. punctilinealis. Anode is to the right, and arrow in A indicates position of sample application.
Fig. 1 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 1. The global distributional range of Aspidoscelis dixoni. This species occurs in two areas that are separated by approximately 500 km from which no specimens are known. The two areas are Antelope Pass, Peloncillo Mountains, Hidalgo County, New Mexico, and Chinati Mountains, Presidio County, Texas. Initialisms are as follows: AZ, Arizona; MX, Mexico; NM, New Mexico; and TX, Texas. Modified from Topo USA 2.0, DeLorme, Yarmouth, Maine (1999).
Fig. 4 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 4. Ventral views (black-and-white) of two of the same lizards shown in figure 3. Upper, hybrid (AMNH R-148141); lower, A. t. punctilinealis (AMNH R-148113). In A. dixoni C (no photograph of ventral view) there is no black on the abdomen or throat, although there may be a few small black dots on the chest.
Fig. 2 in Hybridization Between the Endangered Unisexual Gray-Checkered Whiptail Lizard (Aspidoscelis dixoni) and the Bisexual Western Whiptail Lizard (Aspidoscelis tigris) in Southwestern New Mexico
Fig. 2. Cherry array with drift fence and pitfall traps, where one of the hybrids was found, Antelope Pass, Peloncillo Mountains, Hidalgo County, New Mexico. Photo by C.J.C., June 8, 1990.
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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.