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Figure 6 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 6. Diogenes curvimanus. ♂ 2.6 mm, Guadalquivir N.P., Huelva, Spain, neotype, (MNHN-IU-2019-3214): A, left cheliped, outer aspect; B, left cheliped, dorsal aspect; D, left pereiopod 2 (insets: variations in P3 carpus; dactylus inner aspect); E, left pereiopod 4, outer aspect; F, telson, dorsal aspect; G, merus, mesial view (setae omitted). Diogenes curvimanus. ♀ 2.9 mm, Ría de Arousa, Galicia, Spain (ZSMA2019 0399): C, Left cheliped, outer aspect (arrow indicating bispinose protuberance). (Scales: A–B, G = 1 mm; C, E–F = 0.5 mm; D = 2.0 mm).
Figure 3 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 3. Diogenes armatus sp. nov. ♂ 3.4 mm, Torregorda, Cádiz, Spain, holotype, (MNHN-IU-2019-3213): A, anterior part of body; B, right antennule, inner aspect; C, ophtalmic scales; D, left maxiliped 3 (inset: detail of the spines, ventral aspect); E, right cheliped, dorsal aspect; F, left pereiopod 2 (insets: variations in P3 carpus; dactylus inner aspect); G, telson, dorsal view. (Scales: A, E–G = 1 mm, B–D = 0.5 mm).
Figure 4 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 4. Diogenes armatus sp. nov. ♂ 3.4 mm, Torregorda, Cádiz, Spain, holotype, (MNHN-IU-2019-3213): A, male left cheliped, outer aspect (arrow indicating bispinose protuberance); B, left cheliped, dorsal aspect; C, left cheliped inner surface; D, left cheliped dactylus, dorsal aspect; F, left pereiopod 4, outer aspect; G, left cheliped merus, mesial view (setae omitted). Diogenes armatus sp. nov. ♀ 3.8 mm, Isla Canela, Huelva, Spain, allotype, (MNHN-IU-2014-5736): E, female left cheliped, outer aspect. (Scales: A, C, G = 2 mm; B, D, E = 1 mm; F = 0.5 mm).
Figure 5 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 5. Diogenes curvimanus. ♂ 2.6 mm, Guadalquivir N.P., Huelva, Spain, neotype, (MNHN-IU-2019-3214): A, anterior part of body; B, right antennular, inner aspect; C, ophtalmic scales; D, maxiliped 3 (inset: detail of the spines, ventral aspect); E, right cheliped, outer aspect. (Scales: A = 1 mm, B = 0.2 mm, C–E = 0.5 mm).
Figure 2. Diogenes pugilator s.s in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 2. Diogenes pugilator s.s. ♂ 3.0 mm, Frontignan, France, neotype, (MNHN-IU-2019-3215): A, left cheliped, outer aspect (arrow indicating bispinose protuberance); B, left cheliped, dorsal aspect (inset: detail of the row of tubercles on the lower, inner surface). Diogenes pugilator s.s. ♀ 2.5 mm, La Carihuela, Málaga, Spain, topotype, (IEOCD-BR/2660-2661): C, left cheliped, outer aspect. Diogenes pugilator s.s. ♂ 2.7 mm Frontignan, France, topotype, (ZSMA2019 0400): D, left pereiopod 2 (insets: variations in P3 carpus; dactylus inner aspect); E, pereiopod 4; F, merus, mesial view (setae omitted). (Scales: A–C, F = 2 mm, D = 1 mm, E = 0.5 mm).
Figure 1. Diogenes pugilator s.s in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 1. Diogenes pugilator s.s. ♂ 3.0 mm, Frontignan, France, neotype, (MNHN-IU-2019-3215): A, anterior part of body; B, ophtalmic scales; E, right cheliped, outer aspect; F, telson, dorsal aspect. Diogenes pugilator s.s. ♂ 2.7 mm, Frontignan, France, topotype (ZSMA2019 0400): C, right antennular, inner view; D, left maxiliped 3, (inset: detail of the spines, ventral aspect). (Scales: A, C, E = 1 mm, B, D, F = 0.5 mm).
The research of River Morphology transition and Sediment variation: Shule River, Northwest of China
<p>The morphological features of the Shule River DFS are summarized based on remote sensing image data. It is fan-shaped and nearly symmetric, with a radius of 59.6 km, arc length of 128 km, chord length of 113 km and fan apex angle of 96°, covering an overall area of 3660 km<sup>2</sup>. According to the differences in geomorphological features, slope and river morphology, the Shule River DFS can be divided into the proximal, medial and distal portions (Fig 2). The proximal portion is geomorphologically characterized by the coverage of gravel Gobi, the medial portion by the presence of psammophytic vegetations, and the distal portion by oasis plain. There is a trend of descending slope from the proximal portion through the medial proportion to distal portion (Fig.2). River morphology grades from large-scale braided at the proximal portion through bifurcating braided at the medial portion to meandering at the distal portion. The differences in type of sedimentary microfacies and sedimentary characteristics allow us to determine the distribution law and distribution model of sedimentary facies under modern branched river system.</p>
Dataset of "Graphite lubrication of highly loaded contacts: humidity-dependent friction and structural transition to turbostratic carbon"
<p>Initial atomic configurations for DFTB-MD simulations (Fig. 8-10, Fig. S7).</p>
Factors on the Mesozoic transition from flat to steep subduction of the Paleo-Pacific Plate beneath South China: Thickened oceanic crust and subduction rate
<p>This dataset contains simulation results used for visualizing Figures in "Factors on the Mesozoic transition from flat to steep subduction of the Paleo-Pacific Plate beneath South China: Thickened oceanic crust and subduction rate"</p>
Figure data sets for the paper "Coherent optical-microwave interface for manipulation of low-field electronic clock transitions in 171Yb3+:Y2SiO5"
<p>Figure data sets.</p>
Monte Carlo data for "Melting of generalized Wigner crystals in transition metal dichalcogenide heterobilayer Moiré systems"
<p>Monte Carlo lattice configuration snapshots used to produce the results in the paper "Melting of generalized Wigner crystals in transition metal dichalcogenide heterobilayer Moiré systems." For further details and analysis scripts, see the associated Github repository at https://github.com/KimGroup/tmd_moire_monte_carlo.</p>
Figure 11 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 11. Illustration showing how marine incursion could drive sea–land transition and diversification of the M. japonica complex. A, marine incursion leads to large-scale sea–land transition. B, isolation caused by subsequent marine regression drives terrestrial species diversification. C, stepping-stone dispersal maintains gene flow between different regions. Arrows show the direction of dispersal.
Figure 10 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 10. Morinoia aosen sp. nov. female paratype, from Beijing. A, antennae I–II. B, gnathopod I. C, gnathopod II. D, propodus of gnathopod II. E, pleopod. F, the tip of spine (on the propodus of gnathopod II).
Figure 9 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 9. The telson in Morinoia species. A, B, telson of Morinoia aosen sp. nov. C, telson of M. paludosus. D, telson of M. japonica. White arrows show the interspecific difference. Images of M. paludosus and M. japonica modified from Cheng et al. (2011).
Figure 7 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 7. Morinoia aosen sp. nov. male holotype, from Beijing. A, pereopod III. B, pereopod IV. C, pereopod V. D, pereopod VI. E, pereopod VII.
Figure 8 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 8. The uropod III in Morinoia species. A, B, uropod III of Morinoia aosen sp. nov. C, D, uropod III of M. japonica. E–G, uropod III of M. paludosus. White arrows show the interspecific difference and black arrows show the intraspecific difference. Images of M. paludosus and M. japonica modified from Cheng et al. (2011).
Figure 3 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 3. Population structure of Morinoia japonica species complex based on COI haplotypes. A, minimum spanning network. Each circle represents a unique mitochondrial COI haplotype, with size proportional to frequency. B, assignment of 89 COI haplotypes to K = 5 genetic clusters inferred from STRUCTURE simulations. Colours indicate posterior probability of assignment of each individual to a particular cluster based on the combination of ten replicate runs.
Figure 4 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 4. Morinoia aosen sp. nov. from Beijing. A, male, holotype, IZCAS-I-A1700–1, 8.5 mm. B, female, paratype, IZCASI-A1700–2, 7.6 mm.
Figure 1 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 1. Map of East Asia showing sampling sites. Different-coloured dots correspond to different species delimited by ABGD: Morinoia aosen sp. nov. (red), M. paludosus (green), M. japonica (blue), M. sp1 (green), M. sp2 (pink), M. sp3 (light purple), M. sp4 (purple) and M. sp5 (yellow). White dots represent the coastal Platorchestia pacifica species complex.
Figure 2. A in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 2. A, time-calibrated tree obtained from BEAST 2 based on concatenated loci. The divergence times and 95% highest posterior density are showed at nodes of interest. The sea–land transition occurred about 15.63 Mya, corresponding with the divergence between coastal Platoechestia pacifica and terrestrial Morinoia japonica. The ancestral range reconstructions from the DEC+j model in BioGeoBEARS are indicated at the internal nodes. The bars and species at the right of the tree were inferred from species delimitation based on K2P distance. B, biogeographical reconstruction of stepping-stone dispersal in M. japonica from the Japanese islands to north-eastern continental China. C, sea-level fluctuations (blue line) modified from Miller et al. (2005). The light blue vertical shading indicates the Miocene marine incursion during a high sea-level period.
ScienceDex guides
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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.