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zenodo32/100

FIGURE 4 in A new species of the genus Raphidopus Stimpson, 1858 (Crustacea: Decapoda: Anomura: Porcellanidae) from Peninsular Malaysia, with additional records of R. johnsoni Ng & Nakasone, 1994 from Southeast Asia, and a key to species in the genus

FIGURE 4. Raphidopus Johnsoni Ng & Nakasone, 1994, male (cl 5.0 mm), CBM-ZC 12485, PhUket. A, carapace and ocUlar and antennal pedUncles, dorsal vieW (marginal setae not draWn on right side); B, right branchial margin of carapace, dorsomesial vieW; C, rostrUm, dorso-anterior vieW; D, third and foUrth thoracic sternites, ventral vieW (setae not draWn on left side); E, telson, external vieW; F, basal article of left antennUlar pedUncle, ventral vieW; G, left ocUlar and antennal pedUncles, dorsolateral vieW; H, left third maxilliped, lateral vieW; I, left second pereopod, lateral vieW; J, left second pereopod, merUs, mesial vieW (short striae not draWn); K, left second pereopod, dactylUs, lateral vieW (setae not draWn); L, left third pereopod, lateral vieW (setae and short striae not draWn); M, left third pereopod, merUs, mesial vieW (short striae not draWn); N, left foUrth pereopod, lateral vieW (setae and short striae not draWn); O, left foUrth pereopod, merUs, mesial vieW (short striae not draWn). Scale bars = 1.0 mm.

opennotspecifiedJun 2018View details →
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FIGURE 5 in A new species of the genus Raphidopus Stimpson, 1858 (Crustacea: Decapoda: Anomura: Porcellanidae) from Peninsular Malaysia, with additional records of R. johnsoni Ng & Nakasone, 1994 from Southeast Asia, and a key to species in the genus

FIGURE 5. Raphidopus Johnsoni Ng & Nakasone, 1994, male (cl 4.7 mm), CBM-ZC 12485, PhUket. A, larger cheliped, dorsal vieW; B, larger cheliped, merUs and carpUs, ventral vieW; C, larger cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre on palm and dactylUs not draWn); D, smaller cheliped, dorsal vieW (sUrface strUctUre not draWn); E, smaller cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre not draWn). Setae are not draWn on all figUres. Scale bars = 1.0 mm.

opennotspecifiedJun 2018View details →
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FIGURE 7. Raphidopus brevipes n in A new species of the genus Raphidopus Stimpson, 1858 (Crustacea: Decapoda: Anomura: Porcellanidae) from Peninsular Malaysia, with additional records of R. johnsoni Ng & Nakasone, 1994 from Southeast Asia, and a key to species in the genus

FIGURE 7. Raphidopus brevipes n. sp., paratypes, chelipeds detached from bodies, ZRC 1992.10522–10526, Penang. A, largest larger cheliped, dorsal vieW; B, largest larger cheliped, merUs and carpUs, ventral vieW (sUrface strUctUre not draWn); C, largest larger cheliped, carpUs, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); D, largest larger cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); E, smaller cheliped, dorsal vieW (sUrface strUctUre partially draWn); F, smaller cheliped, carpUs, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); G, smaller cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); H, second largest larger cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre not draWn). Setae are not draWn on all figUres. Scale bars = 1.0 mm.

opennotspecifiedJun 2018View details →
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FIGURE 6. Raphidopus brevipes n in A new species of the genus Raphidopus Stimpson, 1858 (Crustacea: Decapoda: Anomura: Porcellanidae) from Peninsular Malaysia, with additional records of R. johnsoni Ng & Nakasone, 1994 from Southeast Asia, and a key to species in the genus

FIGURE 6. Raphidopus brevipes n. sp., holotype, male (cl 5.8 mm), ZRC 1992.10521, Penang. A, carapace and ocUlar and antennal pedUncles, dorsal vieW (setae not draWn); B, rostrUm, dorso-anterior vieW; C, anterior part of left pterygostomial flap, ventrolateral vieW; D, third and foUrth thoracic sternites, ventral vieW (setae not draWn); E, telson, external vieW; F, basal article of left antennUlar pedUncle, ventral vieW; G, left ocUlar and antennal pedUncles, dorsolateral vieW (setae not draWn); H, left third maxilliped, lateral vieW (setae not draWn). Scale bars = 1.0 mm.

opennotspecifiedJun 2018View details →
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FIGURE 3 in A new species of the genus Raphidopus Stimpson, 1858 (Crustacea: Decapoda: Anomura: Porcellanidae) from Peninsular Malaysia, with additional records of R. johnsoni Ng & Nakasone, 1994 from Southeast Asia, and a key to species in the genus

FIGURE 3. Raphidopus Johnsoni Ng & Nakasone, 1994, holotype, male (cl 3.8 mm), ZRC 1992.10669, Singapore. A, carapace and ocUlar and antennal pedUncles, dorsal vieW (transverse striae and ridges not draWn); B, rostrUm, dorso-anterior vieW; C, third and foUrth thoracic sternites, ventral vieW; D, basal article of left antennUlar pedUncle, ventral vieW; E, left third maxilliped, lateral vieW (sUrface strUctUre not draWn); F, larger cheliped, merUs, ventral vieW (sUrface strUctUre not draWn); G, larger cheliped, carpUs, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); H, larger cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); I, smaller cheliped, carpUs, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); J, smaller cheliped, chela, dorsal perpendicUlar vieW (sUrface strUctUre not draWn); K, left foUrth pereopod, lateral vieW (short striae not draWn); L, same, merUs, lateral perpendicUlar vieW (short striae not draWn). Setae are not draWn on all figUres. Scale bars = 1.0 mm.

opennotspecifiedJun 2018View details →
zenodo32/100

Data file for paper: Javier Rubio-Garcia; Anthony R J Kucernak, and Alexandra Charleson, "Direct visualization of reactant transport in forced convection electrochemical cells and its application to Redox Flow Batteries, Electrochemistry Communications, 2018

<p>Excel Data file containing the data presented in the figures of the paper:</p> <p>Javier Rubio-Garcia; Anthony R J Kucernak, and Alexandra Charleson, &quot;Direct visualization of reactant transport in forced convection electrochemical cells and its application to Redox Flow Batteries</p> <p>Electrochemistry Communications, 2018,</p> <p>DOI:10.1016/j.elecom.2018.07.002</p> <p>Please cite the above reference if you wish to use this data</p>

opencc-by-4.0Jul 2018View details →
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F I G U R E 6 in Dispersal in dendritic networks: Ecological consequences on the spatial distribution of population densities

F I G U R E 6 Euclidean distances moved by Tetrahymena individuals depending on densities in our entire dataset. Across all replicates of all landscapes (patches from different landscapes types highlighted by different symbols; see legend) we find positively densitydependent movement. The solid lines represent fits of the averaged linear mixed model (red: dendritic landscapes; blue: linear landscapes) and the shaded area shows 95% confidence intervals (see Table 4 for model selection results). [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedDec 2017View details →
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F I G U R E 4 in Dispersal in dendritic networks: Ecological consequences on the spatial distribution of population densities

F I G U R E 4 Comparison of variation in population densities between linear and dendritic networks at day 15 of the experiment. The solid line represents the difference between inter-quartile range (IQR) over median population densities of linear and dendritic landscapes. The distribution (grey) represents the distribution of the differences between IQR over median population densities of 200,000 random re-samplings for our data. As we theoretically expect the dendritic landscapes to be more variable we can perform a one-sided test which gives a probability of p =.047 of our observed difference between IQR to median ratios to be larger than zero. [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedDec 2017View details →
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F I G U R E 3 in Dispersal in dendritic networks: Ecological consequences on the spatial distribution of population densities

F I G U R E 3 Fit of theoretical expectations to the distribution of Tetrahymena population densities depending on network type (linear versus dendritic networks), network position (central versus inner versus outer nodes) for day 15. Violin plots show the overall distribution of the data, the white point gives the median, and the solid black line the 25% and 75% percentiles, respectively. Given the network structure (Figure 1) and the three replicates per landscape, distributions include N = 18 (9, 3) measurements for outer (inner, central) nodes of dendritic networks and N = 6 (6, 18) measurements for outer (inner, central) nodes of linear landscapes. Horizontal red and blue lines visualise fits of the theoretically expected distribution of population densities to data from the dendritic and linear networks assuming network specific dispersal rates (d) and carrying capacities (K). White squares show fits of the theoretically expected distribution of population densities assuming the same d and K values for both network types. Shaded areas, respectively, error bars, show 95% confidence intervals of the fits. [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedDec 2017View details →
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F I G U R E 2 in Dispersal in dendritic networks: Ecological consequences on the spatial distribution of population densities

F I G U R E 2 Distribution of Tetrahymena population densities depending on network type (linear versus dendritic networks), network position (central versus inner versus outer nodes) and time (days 0, 8 and 15). Violin plots show the overall distribution of the data, the white point gives the median, and the solid black line the 25% and 75% percentiles, respectively. Given the network structure (Figure 1) and the three replicates per landscape, distributions include N = 18 (9, 3) measurements for outer (inner, central) nodes of dendritic networks and N = 6 (6, 18) measurements for outer (inner, central) nodes of linear landscapes. Horizontal lines visualise back-transformed parameter estimates of the averaged linear mixed effects model and shaded areas show 95% confidence intervals (see Table 2 for model selection results). [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedDec 2017View details →
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F I G U R E 1 in Dispersal in dendritic networks: Ecological consequences on the spatial distribution of population densities

F I G U R E 1 Median population densities (in thousands of individuals) of Tetrahymena in corresponding dendritic (a) and linear (b) landscapes at the end of the experiment (day 15) and across the three replicate landscapes. In these landscapes, outer nodes are labelled "O," inner and central nodes are labelled "I" and "C", respectively. [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedDec 2017View details →
zenodo32/100

F I G U R E 5 in Dispersal in dendritic networks: Ecological consequences on the spatial distribution of population densities

F I G U R E 5 Euclidean distances moved by Tetrahymena individuals depending on network type (linear versus dendritic networks), network position (central versus inner versus outer nodes) and time (days 0, 8 and 15). Violin plots show the overall distribution of the data, the white point gives the median, and the solid black line the 25% and 75% percentiles, respectively. Given the network structure (Figure 1) and the three replicates per landscape distributions include N = 18 (9, 3) measurements for outer (inner, central) nodes of dendritic networks and N = 6 (6, 18) measurements for outer (inner, central) nodes of linear landscapes. Horizontal lines visualise back-transformed parameter estimates of the averaged linear mixed effects model and shaded areas show 95% confidence intervals (see Table 3 for model selection results). [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedDec 2017View details →
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Supplementary data to the manuscript "Morphology and metabarcoding! A test with stream diatoms from Mexico highlights the complementarity of methods", submitted to Freshwater Science by D. Mora, N. Abarca, S. Proft, J. Grau, N. Enke, J. Carmona, O. Skibbe, R. Jahn and J. Zimmermann.

<p>Demultiplexed fastq files for 18 samples, accompanied by a table including sample numbers in the manuscript and sample numbers in the fastq files.</p>

opencc-by-4.0Jul 2018View details →
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Supplementary material 1 from: Short G, Smith R, Motomura H, Harasti D, Hamilton H (2018) Hippocampus japapigu, a new species of pygmy seahorse from Japan, with a redescription of H. pontohi (Teleostei, Syngnathidae). ZooKeys 779: 27-49. https://doi.org/10.3897/zookeys.779.24799

Genetic distance analysis (uncorrected p distances) of COI sequence data from 21 specimens of H.pontohi and those referred to H.severnsi :

opencc-zeroAug 2018View details →
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FIGURE 5a–r in Immature stages of the genus Oxythyrea (Coleoptera: Scarabaeidae: Cetoniinae) with a key to third instar larvae, and notes on the biology of the genus

FIGURE 5a–r. Epipharynx of third instar Oxythyrea larvae (a–i) and antenna of third instar Oxythyrea larvae, ventral aspect (j–r). a, O. abigail; b, O. albopicta; c, O. cinctella; d, O. dulcis; e, O. funesta; f, O. noemi; g, O. pantherina; h, O. subcalva; i, O. tripolitana; j, O. abigail; k, O. albopicta; l, O. cinctella; m, O. dulcis; n, O. funesta; o, O. noemi; p, O. pantherina; q, O. subcalva; r, O. tripolitana. Scale bars = 0.5 mm.

opennotspecifiedSep 2018View details →
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FIGURE 4a–r in Immature stages of the genus Oxythyrea (Coleoptera: Scarabaeidae: Cetoniinae) with a key to third instar larvae, and notes on the biology of the genus

FIGURE 4a–r. Cranium of third instar Oxythyrea larvae (a–i) and antenna of third instar Oxythyrea larvae, dorsal aspect (j–r). a, O. abigail; b, O. albopicta; c, O. cinctella; d, O. dulcis; e, O. funesta; f, O. noemi; g, O. pantherina; h, O. subcalva; i, O. tripolitana; j, O. abigail; k, O. albopicta; l, O. cinctella; m, O. dulcis; n, O. funesta; o, O. noemi; p, O. pantherina; q, O. subcalva; r, O. tripolitana. Scale bars = 1 mm (a–i); 0.5 mm (j–r).

opennotspecifiedSep 2018View details →
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FIGURE 10a–r in Immature stages of the genus Oxythyrea (Coleoptera: Scarabaeidae: Cetoniinae) with a key to third instar larvae, and notes on the biology of the genus

FIGURE 10a–r. Last abdominal segment of third instar Oxythyrea larvae, ventral view (a–i) and last abdominal segment of third instar Oxythyrea larvae, detail of raster (j–r). a, O. abigail; b, O. albopicta; c, O. cinctella; d, O. dulcis; e, O. funesta; f, O. noemi; g, O. pantherina; h, O. subcalva; i, O. tripolitana; j, O. abigail; k, O. albopicta; l, O. cinctella; m, O. dulcis; n, O. funesta; o, O. noemi; p, O. pantherina; q, O. subcalva; r, O. tripolitana. Scale bars = 1 mm (a–i).

opennotspecifiedSep 2018View details →
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FIGURE 180. H. melpomene amaryllis C. Felder & R. Felder, 1862 in Alternative facts: a reconsideration of putatively natural interspecific hybrid specimens in the genus Heliconius (Lepidoptera: Nymphalidae)

FIGURE 180. H. melpomene amaryllis C. Felder &amp; R. Felder, 1862 (dorsal, ventral). Peru: San Martín, Satipo. (image source: https://cliniquevetodax.com/Heliconius/pages/melpomene%20amaryllis.html).

opennotspecifiedOct 2018View details →
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FIGURE 171. H. peruvianus C. Felder & R. Felder, 1859 in Alternative facts: a reconsideration of putatively natural interspecific hybrid specimens in the genus Heliconius (Lepidoptera: Nymphalidae)

FIGURE 171. H. peruvianus C. Felder &amp; R. Felder, 1859 (dorsal). Ecuador: "Esmeraldas, Lita, Chuchuví" (locality data erroneous—K. Willmott pers. comm.). (image source: https://cliniquevetodax.com/Heliconius/pages/peruvianus.html). This taxon, elevated from subspecific status by Jiggins &amp; Davies (1998), is a dry-forest segregate from western Ecuador like H. himera.

opennotspecifiedOct 2018View details →
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FIGURE 179. H. ethilla aerotome C. Felder & R. Felder 1862 in Alternative facts: a reconsideration of putatively natural interspecific hybrid specimens in the genus Heliconius (Lepidoptera: Nymphalidae)

FIGURE 179. H. ethilla aerotome C. Felder &amp; R. Felder 1862 (dorsal, ventral). Peru: San Martín, Juanjui. (image source: https://cliniquevetodax.com/Heliconius/pages/ethilla aerotome.html). Note the tawny shading of the distal FW, and the yellowish tint of the transverse band on the HWV.

opennotspecifiedOct 2018View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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