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FIGURE 6. Hybrid form Bythotrephes brevimanus x B in Morphological assessment of the North Eurasian interspecific hybrid forms of the genus Bythotrephes Leydig, 1860 (Crustacea: Cladocera: Cercopagididae)
FIGURE 6. Hybrid form Bythotrephes brevimanus x B. cederströmii, females (A–G). Bythotrephes sp. x B. cederströmii, females (H–M). (A–F, Lake Gusinoe; G, Lake Zaysan; H–M, Lake Borzu-Khol'). A–E, J, K, postabdominal and caudal claws. F, L, M, bend of caudal process. G, I, setae of distal end of second endopodital segment of tl I. H, the same of first endopodital segment of tl I.
High resolution crystallographic and chemical characterisation of iodine induced stress corrosion crack tips formed in irradiated and non-irradiated zirconium alloys - Supporting data
<p>Data related to High resolution crystallographic and chemical characterisation of iodine induced stress corrosion crack tips formed in irradiated and non-irradiated zirconium alloys:</p> <p>Conor Gillen, Alistair Garner, Pia Tejland, Philipp Frankel,<br> High resolution crystallographic and chemical characterisation of iodine induced stress corrosion crack tips formed in irradiated and non-irradiated zirconium alloys, Journal of Nuclear Materials, Volume 519, 2019, Pages 166-172, ISSN 0022-3115,<br> https://doi.org/10.1016/j.jnucmat.2019.03.027.</p> <p>Datafiles for STEM-EDX analysis - STEM-EDX.zip</p> <p>Datafiles for TKD analysis - TKD.zip</p> <p>Datafiles for NanoSIMS analysis - 1: NanoSIMS raw data file (.im file) with all 160 planes and data for all ion signals acquired. Can be opened with the OpenMIMS plugin for ImageJ or other NanoSIMS software. 2: NanoSIMS processed data file (.nrrd file) which is drift corrected and can be opened with the OpenMIMS plugin for ImageJ</p>
text-fig. 28. Sacra of theropod dinosaurs, illustrating different states for character 116. a, sacrum and ilium of Herrerasaurus ischigualastensis in lateral view; the shaded area indicates the attachment area of the very massive sacral ribs on the medial side of the ilium; modified from Novas (1993). B, sacrum and ilia of Syntarsus rhodesiensis in dorsal view, showing the almost continuous sheet of bone formed by the sacral ribs between the sacrum and the iliac blades; based on Raath (1990) and QG1. Abbreviations: ib, iliac blade; il, ilium; ns: neural spine; SI, S2, sacral vertebrae; sac, supraacetabular crest; sr, sacral ribs; st, spine table. Scale bars represent 50 mm. in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 28. Sacra of theropod dinosaurs, illustrating different states for character 116. a, sacrum and ilium of Herrerasaurus ischigualastensis in lateral view; the shaded area indicates the attachment area of the very massive sacral ribs on the medial side of the ilium; modified from Novas (1993). B, sacrum and ilia of Syntarsus rhodesiensis in dorsal view, showing the almost continuous sheet of bone formed by the sacral ribs between the sacrum and the iliac blades; based on Raath (1990) and QG1. Abbreviations: ib, iliac blade; il, ilium; ns: neural spine; SI, S2, sacral vertebrae; sac, supraacetabular crest; sr, sacral ribs; st, spine table. Scale bars represent 50 mm.
Fig. 4 Usnea parafloridana K in Evaluation of traditionally circumscribed species in the lichen-forming genus Usnea, section Usnea (Parmeliaceae, Ascomycota) using a six-locus dataset
Fig. 4 Usnea parafloridana K. Mark, Will-Wolf & Randlane sp. nov. – view of general habit (a, b), soralia with isidiomorphs (c), fibrils (d), soralia (e), and branch anatomy (f). Scale bars 7 mm (a, b), 1.5 mm (c), 2 mm (d), 0.4 mm (e), and 0.3 mm (f). Photographed specimens WW14807 (holotype; a, c, e), WW14858 (b, d), and WW14857 (f)
Fig. 3 in Evaluation of traditionally circumscribed species in the lichen-forming genus Usnea, section Usnea (Parmeliaceae, Ascomycota) using a six-locus dataset
Fig. 3 STACEY maximum clade credibility SMC-tree with posterior probabilities (PP) from STACEY (above branches) and *BEAST (below) analyses together with similarity matrix for the section Usnea dataset. The squares represent posterior probabilities (white = 0, black = 1) for pairs of individuals to belong to the same cluster. The lines in the matrix separate major groups (named above matrix), while
Fig. 1 Bayesian 50 in Evaluation of traditionally circumscribed species in the lichen-forming genus Usnea, section Usnea (Parmeliaceae, Ascomycota) using a six-locus dataset
Fig. 1 Bayesian 50 % consensus tree of 18 currently accepted Usnea species based on six concatenated loci, inferred by BEAST. Major groups and secondary chemistry are indicated right of the tree. Branch supports are given in circles: Black circles reflect strong support from both inferences (PP ≥ 95 % for BEAST and BP ≥ 70 % for RAxML), and gray circles strong support from BEAST only. Location and laboratory code are given in brackets. Scale bar shows the number of substitutions per site. Secondary metabolites: BAR barbatic acid, BMY baeomycesic
Fig. 2 in Evaluation of traditionally circumscribed species in the lichen-forming genus Usnea, section Usnea (Parmeliaceae, Ascomycota) using a six-locus dataset
Fig. 2 Box plots of cortex (a, d) and medulla (b, e) thickness measurements and bar charts of medulla density categories (c, f) in clades barbata-chaetophora-dasopoga-diplotypus (bar-das-dip) and barbata-intermedia-lapponica-substerilis (bar-int-lap; first row of charts), and between Usnea barbata specimens from these clades (second row of charts). Box plots show the percentages of the whole width of the measured branch. Center lines are the medians, box limits indicate the 25th and 75th percentiles as determined by R software, whiskers extend
Fig. 14 in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 14 Holotype (FMNH 189250) of Ichthyophis youngorum in preservative (TL, 208.0 mm). Photographs by Harry Taylor
Fig. 10 a, b in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 10 a, b Holotype (ZFMK 88976) of Ichthyophis catlocensis sp. nov. in life (TL, 183.5 mm) from Cat Loc, Cat Tien National Park, Lam Dong Province, southern Vietnam. a General view. Photograph by PG; b close up of the head. Photograph by E.A. Galoyan
Fig. 5 a–f in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 5 a–f Jaws of the holotype of (depicted characters are also present in the respectively investigated paratype specimens): a Ichthyophis cardamomensis sp. nov. (LSUHC 9335), b Ichthyophis catlocensis sp. nov. (ZFMK 88976), c Ichthyophis chaloensis sp. nov. (IEBR A.2011.16), d Ichthyophis laosensis (MNHN 1928.95), e Ichthyophis acuminatus (AMNH A20875), and f Ichthyophis youngorum (FMNH 189250). Drawings by PG
Fig. 3 in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 3 The ML tree of Ichthyophiidae derived from the analysis of 1296 bp of cyt b mtDNA gene. Uraeotyphlus oxyurus and "Ichthyophis" bombayensis are used as outgroups. Node support values (BS, 1000 replicates PP for Bayesian Inference) are shown above or below tree nodes for ML/MP/BI analyses, respectively. Those species of Ichthyophiidae sensu lato which lack lateral stripes are shaded with dark grey
Fig. 2 in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 2 ML tree illustrating phylogenetic relationships of Ichthyophis species based on the analysis of 660 bp of COI and 1296 bp of cyt b mtDNA gene. Node support values (BS, 1000 replicates PP for Bayesian
Fig. 7 a–f in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 7 a–f Holotype (LSUHC 9335) of Ichthyophis cardamomensis sp. nov. in preservative (TL, 183.0 mm). Photographs by PG
Fig. 4 in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 4 Holotype (AMNH A20875) of Ichthyophis acuminatus in preservative (TL, 294.0 mm). Photographs by HM
Fig. 6 a–f in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 6 a–f Tail region (in ventral view) of the holotype specimens of: a Ichthyophis cardamomensis sp. nov. (LSUHC 9335), b Ichthyophis catlocensis sp. nov. (ZFMK 88976), c Ichthyophis chaloensis sp. nov. (IEBR A.2011.16), d Ichthyophis laosensis (MNHN 1928.95), e Ichthyophis acuminatus (AMNH A20875), and f Ichthyophis youngorum (FMNH 189250). Drawings by PG
Fig. 11 in New Ichthyophis species from Indochina (Gymnophiona, Ichthyophiidae): 1. The unstriped forms with descriptions of three new species and the redescriptions of I. acuminatus Taylor, 1960, I. youngorum Taylor, 1960 and I. laosensis Taylor, 1969
Fig. 11 Holotype (IEBR A.2011.15) of Ichthyophis chaloensis sp. nov. in preservative (TL, 215.7 mm). Photographs by PG
Fig. 6 in Not the same: phylogenetic relationships and ecological niche comparisons between two different forms of Aglaoctenus lagotis from Argentina and Uruguay
Fig. 6 Annual and sexual niches overlap comparisons between the three forms of A. lagotis: A comparisons between Form I and Form IIa (annual niche above, sexual niche below); B comparisons between Form I and Form IIb (annual niche above, sexual niche below); C comparisons between Form IIb and Form IIa (annual niche above, sexual niche below). The overlap is represented along two principal component analysis (PCA) calibrated axes, the solid and dashed contour lines illustrate 100% and 50%, respectively, of the available (background) environment. Color shading represents the density of the occurrences by cell. The similarity tests between the compared forms were calculated from 100 iterations
Fig. 2 in Not the same: phylogenetic relationships and ecological niche comparisons between two different forms of Aglaoctenus lagotis from Argentina and Uruguay
Fig. 2 Map showing the sampling localities for genetic and ecological niche analyses of A. lagotis. Sampled locations are indicated by colored symbols according to the identification of the individuals
Fig. 5 in Not the same: phylogenetic relationships and ecological niche comparisons between two different forms of Aglaoctenus lagotis from Argentina and Uruguay
Fig. 5 Species tree and chronogram inferred from mitochondrial genes (cox1, 12S, and 16S+ L1 + nad1) and the nuclear intron tif5A with *BEAST under partition scheme by gene and strict clock. Numbers above branches denote Bayesian posterior probabilities clade
Fig. 11 in So different but nonetheless the same species: multiple geographic clines explain the diverse forms of the anthidiine bee Rhodanthidium caturigense s.l. (Apoidea: Megachilidae: Anthidiini)
Fig. 11 Evolutionary history of Rhodanthidium caturigense from various parts of the distribution area as inferred by using the maximum likelihood method and Kimura 2-parameter model. Numbers shown
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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.