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13,017 results for “Positionning”
FIGURE 3 in A new species of Phrynopus from the northeastern Andes of Peru, its phylogenetic position, and notes on the relationships of Holoadeninae (Anura: Craugastoridae)
FIGURE 3. Dorsal (A) and ventral (B) views of the female holotype (CORBIDI 11668) of Phrynopus mariellaleo sp. nov. in life. Photographs by Pablo J. Venegas.
FIGURE 2 in A new species of Phrynopus from the northeastern Andes of Peru, its phylogenetic position, and notes on the relationships of Holoadeninae (Anura: Craugastoridae)
FIGURE 2. Dorsal (A) and ventral (B) views, and lateral view of head (C) of the female holotype (CORBIDI 11668) of Phrynopus mariellaleo sp. nov. in preservative (SVL = 39.7). Photographs by Pablo J. Venegas.
FIGURE 1 in A new species of Phrynopus from the northeastern Andes of Peru, its phylogenetic position, and notes on the relationships of Holoadeninae (Anura: Craugastoridae)
FIGURE 1. One optimal tree of 15646 steps depicting the position of Phrynopus mariellaleo sp. nov. and the relationships of other species of Holoadeninae. The tree was inferred from 13269 aligned positions (tree-alignment in POY) of non-coding mtDNA genes 12S, 16S and the intervening tRNAvaline and tRNAleucine, mtDNA coding genes COI and CYTB, and fragments of the nuclear protein-coding genes 28S, C-MYC, CXCR4, H3, NCX1, POMC, RAG1, RHO, SIA, SLC8A3, and TYR. Jackknife frequencies and Goodman-Bremer values are shown above and below nodes, respectively.
FIGURE 4 in A new species of Phrynopus from the northeastern Andes of Peru, its phylogenetic position, and notes on the relationships of Holoadeninae (Anura: Craugastoridae)
FIGURE 4. Paratypes of Phrynopus mariellaleo sp. nov. showing variation in dorsal and ventral external morphological traits. (A, B) adult female (CORBIDI 11692), (C, D) adult female (CORBIDI 11657), and (E, F) adult male (CORBIDI 11658). Photographs by Pablo J. Venegas.
FIGURE 6 in A new species of Phrynopus from the northeastern Andes of Peru, its phylogenetic position, and notes on the relationships of Holoadeninae (Anura: Craugastoridae)
FIGURE 6. Habitat at the type locality of Phrynopus mariellaleo sp. nov. Photograph taken on 21 August 2012 by P.J. Venegas.
FIGURES 42–55 in Revisiting the diversity of Ludioctenus Fairmaire (Elateridae: Agrypninae), with description of a new species from Afghanistan, and discussion on the systematic position of Tetrigusina
FIGURES 42–55. Ludioctenus pakistanicus Schimmel & Tarnawski, 2012, holotype, male. 42, habitus, dorsal view; 43, habitus, ventral view; 44, habitus, lateral view; 45, antenna; 46, pronotum; 47, scutellar shield; 48, interior part of metacoxal plate, 49, abdominal sternite VIII; 50, abdominal tergite VIII; 51, abdominal sternite IX; 52, abdominal sternite X; 53, abdominal tergites IX–X; 54, aedeagus, dorsal view; 55, aedeagus, ventral view. Scale bars = 5.0 mm (Figs 42–44), 2.0 mm (Fig. 45–46), 1.0 mm (Figs 47–55).
FIGURES 29–41 in Revisiting the diversity of Ludioctenus Fairmaire (Elateridae: Agrypninae), with description of a new species from Afghanistan, and discussion on the systematic position of Tetrigusina
FIGURES 29–41. Ludioctenus cyprius (Baudi di Selve, 1871), female (Greece). 29, habitus, dorsal view; 30, habitus, ventral view; 31, habitus, lateral view; 32, antenna; 33, pronotum; 34, scutellar shield; 35, interior part of metacoxal plate, 36, abdominal tergite VII; 37, abdominal tergite VIII and sternite VIII, ventral view; 38, abdominal tergite VIII and sternite VIII, dorsal view; 39, ovipositor, ventral view; 40, ovipositor, dorsal view; 41, female genital tract. Scale bars = 5.0 mm (Figs 29–31, 33), 2.0 mm (Fig. 32–40), 1.0 mm (Figs 34–35, 41).
FIGURES 1–14 in Revisiting the diversity of Ludioctenus Fairmaire (Elateridae: Agrypninae), with description of a new species from Afghanistan, and discussion on the systematic position of Tetrigusina
FIGURES 1–14. Ludioctenus afghanicus sp. nov., holotype, male. 1, habitus, dorsal view; 2, habitus, ventral view; 3, habitus, lateral view; 4, antenna; 5, pronotum; 6, scutellar shield; 7, interior part of metacoxal plate, 8, abdominal sternite VIII; 9, abdominal tergite VIII; 10, abdominal sternite IX; 11, abdominal sternite X; 12, abdominal tergites IX–X; 13, aedeagus, dorsal view; 14, aedeagus, ventral view. Scale bars = 5.0 mm (Figs 1–3, 5), 2.0 mm (Fig. 4), 1.0 mm (Figs 6–14).
FIGURES 56–61. 56 in Revisiting the diversity of Ludioctenus Fairmaire (Elateridae: Agrypninae), with description of a new species from Afghanistan, and discussion on the systematic position of Tetrigusina
FIGURES 56–61. 56, Ludioctenus pakistanicus Schimmel & Tarnawski, 2012, paratype, male? (India), pronotum; 57–61 L. pakistanicus, paratype, female (Pakistan). 57, pronotum; 58, ovipositor; 59, abdominal sternite VIII; 60, female genital tract; 61, abdominal tergite VIII. Scale bars = 5.0 mm (Figs 56–57), 2.0 mm (Figs 58–61).
FIGURES 15–28 in Revisiting the diversity of Ludioctenus Fairmaire (Elateridae: Agrypninae), with description of a new species from Afghanistan, and discussion on the systematic position of Tetrigusina
FIGURES 15–28. Ludioctenus cyprius (Baudi di Selve, 1871), male (Greece). 15, habitus, dorsal view; 16, habitus, ventral view; 17, habitus, lateral view; 18, antenna; 19, pronotum; 20, scutellar shield; 21, interior part of metacoxal plate, 22, abdominal sternite VIII; 23, abdominal tergite VIII; 24, abdominal sternite IX; 25, abdominal sternite X; 26, abdominal tergites IX–X; 27, aedeagus, ventral view; 28, aedeagus, dorsal view. Scale bars = 5.0 mm (Figs 15–17, 19), 2.0 mm (Fig. 18), 1.0 mm (Figs 20–28).
Positive wmax (v = ]175, 250[ m/s)
<p>The proposed model for problem <strong>Positive <em>w<sub>max</sub></em> (<em>v</em> = ]175, 250[ m/s) </strong>is a neural net composite (NNC) given by the sum of 4 ANNs. The <em>W<sub>j-s(i)</sub></em> and <em>b<sub>s(i)</sub></em> arrays for each <em>i </em><sup>th</sup> net are given in W_b(i).xlsx (<em>i </em>= 0,..., 3)</p> <p> </p> <p><strong>Check reference below</strong> (to be added when the paper is published)<br> <br> <a href="https://www.researchgate.net/publication/328849817_11_Neural_Networks_-_Max_Disp_-_Railway_Beams">https://www.researchgate.net/publication/328849817_11_Neural_Networks_-_Max_Disp_-_Railway_Beams</a></p>
Positive wmax (v = [50, 175] U [250, 300] m/s)
<p>The proposed model for problem <strong>Positive <em>w<sub>max</sub></em> (<em>v</em> = [50, 175] U [250, 300] m/s) </strong>is a single neural net. The <em>W<sub>j-s</sub></em> and <em>b<sub>s</sub></em> arrays that represent its unknowns are given in W_b.xlsx </p> <p> </p> <p><strong>Check reference below</strong> (to be added when the paper is published)</p> <p><a href="https://www.researchgate.net/publication/328849817_11_Neural_Networks_-_Max_Disp_-_Railway_Beams">https://www.researchgate.net/publication/328849817_11_Neural_Networks_-_Max_Disp_-_Railway_Beams</a></p>
FIGURE 9 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 9. Paucumara falcata. Photomicrographs: (A) PLA-Pa002, testes; (B–C) PLA-Pa002, penis and musculoparenchymatic organ; (D) PLA-Pa002, female reproductive system; (E) PLA-Pa001, oviducts and bursal canal. Scale bar: 20 µm.
FIGURE 8 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 8. Paucumara falcata. Whole mounts. (A) PLA-N004, entire animal; (B) PLA-N004, testes and ovaries; (C) PLA- N006, penis and musculo-parenchymatic organ; (D) PLA-N005, musculo-parenchymatic organ. Scale bar: A–B = 200 µm, C– D = 50 µm.
FIGURE 6 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 6. Nerpa fistulata. (A) diagrammatic horizontal reconstruction of entire animal, based on examination of several specimens; (B) diagrammatic sagittal reconstruction of the copulatory apparatus, based on examination of several specimens.
FIGURE 5 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 5. Nerpa fistulata. Photomicrographs of sagittal sections. (A–B) PLA-N003, ovaries; (C) PLA-N003, copulatory apparatus; (D) PLA-N003, lateral bursa; (E) PLA-N001, oviduct. Scale bar: 20 µm.
FIGURE 4. Nerpa fistulata. PLA-N004 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 4. Nerpa fistulata. PLA-N004, photomicrographs of horizontal sections. (A) anterior end; (B–F) copulatory apparatus. Scale bar: 20 µm.
FIGURE 11 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 11. Paucumara falcata. (A) diagrammatic reconstruction of the copulatory apparatus, based on examination of several specimens; (B) two animals in copulation. Scale bar: 500 µm.
FIGURE 1 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 1. Bayesian inference phylogenetic tree topology based on 18S rDNA dataset. Numbers on branches indicate support values (posterior probability/bootstrap).
FIGURE 3 in Two new species of marine flatworm from southern China facilitate determination of the phylogenetic position of the genus Nerpa Marcus, 1948 and the histochemical structure of the nervous system in the genus Paucumara Sluys, 1989 (Platyhelminthes, Tricladida, Maricola)
FIGURE 3. Nerpa fistulata. Whole mounts. (A) PLA-N005, whole animal; (B) PLA-N006, penis and oviduct; (C) PLA-N005, penis. Scale bar: A = 100 µm, B–C = 20 µm.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.