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Figure 4 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)

Figure 4. NMDS configuration showing ecological groupings from microhabitat characteristics of Sarawak frogs. Each point represents a species: Hba = Pulchrana baramica (N = 62 individuals), Hg = Pulcharana glandulosa (N = 10 individuals), Hsig = Pulcharana signata (N = 26 individuals), Hp = Pulcharana picturata (N = 27 individuals, Hra = Chalcorana raniceps (N = 112 individuals), He = Hylarana erythraea (N = 46 individuals), and Oh = Odorrana hosii (N = 21 individuals).

opencc-by-4.0Apr 2017View details →
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Figure 2 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)

Figure 2. Dendrogram of Morisita's similarity resulting from average linkage clustering using the unweighted pair-group (UPGMA) method on data based on counts of individuals of frogs' species associated with habitats and microhabitats.

opencc-by-4.0Apr 2017View details →
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Figure 3 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)

Figure 3. Final coordinate dimension (FDC) 1(A) and 2(B) of NMDS (PROXSCAL) of microhabitat characteristics of Sarawak frogs.

opencc-by-4.0Apr 2017View details →
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Figure 2 in Interspecific and intraspecific size and shape variation in skull of two closely related species Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) from Turkey

Figure 2. Location of 17 two-dimensional landmarks on the dorsal (A) and ventral (B) skull side of a common toad. A. Dorsal side: 1. Snout tip, 2. Anterior end of suture between premaxilla and maxilla, 3. Anterior end of nasal, 4. Lateralmost point of nasal, 5. Mostanterior point of frontoparietal, 6. Lateralmost point of nasal (posterior), 7. Middle point of the median edge of frontoparietal, 8. Mostposterior median point of frontoparietal, 9. Posterior end of suture between frontoparietal and prootic, 10. Anterior end of suture between frontoparietal and prootic, 11. Middle point of the lateral edge of frontoparietal, 12. Mostanterior point of squamosal, 13. Posterior end of squamosal in contact with prootic, 14. Mostposterior point of prootic, 15. Mostposterior point of maxilla, 16. Posterior end of quadrate, 17. Medial tip of occipital. B. Ventral side: 1. Anteriormost point of premaxilla, 2. Anteriolateral end of premaxilla, 3. Mostposterior median end of premaxilla, 4. Posteriolateral end of premaxilla, 5. Lateralmost point of vomer, 6. Mostposterior end of vomer, 7. Most median point of palatine, 8. Anteriolateral end of palatine, 9. Posteriolateral end of palatine (anterior end of suture between palatine and pterygoid or anterior end of pterygoid), 10. Posteriomedian end of pterygoid, 11. Posteriolateral end of pterygoid, 12. Lateralmost end of parasphenoid, 13. Mostanterior median end of parasphenoid, 14. Mostposterior median end of parasphenoid, 15. Posterior end of maxilla in contact with quadratojugal, 16. Posterior end of quadratojugal, 17. Mostposterior end of occipital condyl.

opencc-by-4.0Mar 2021View details →
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Figure 1 in Interspecific and intraspecific size and shape variation in skull of two closely related species Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) from Turkey

Figure 1. Distribution map of Bufo bufo (blue) and Bufo verrucosIssImus (yellow) in Turkey according to IUCN Red List and Özdemir et al. (2020), and geographical positions of analysed populations.

opencc-by-4.0Mar 2021View details →
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Figure 3 in Interspecific and intraspecific size and shape variation in skull of two closely related species Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) from Turkey

Figure 3. The positions of the specimens in morphospaces defined by the first two principal axes derived from covariance matrices of skull shape variables. Blue dots; B. bufo, yellow dots; B. verrucosissimus. DC: dorsal cranium, VC: ventral cranium.

opencc-by-4.0Mar 2021View details →
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Figure 6 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 6: Centruroides edwardsii. Female. A–C from Sierra de Macuira, La Guajira, Colombia (RTO: Sco-0374); D–E from Tilarán, Guanacaste, Costa Rica (MM-S009). A, dorsal; B, ventral aspect; C–D, telson, lateral aspect. E, pedipalp chela, dorsal aspect.

opencc-by-4.0Nov 2011View details →
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Figure 7 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 7: Centrurus gambiensis. Male holotype. A-B, dorsal (A) and ventral (B) aspect, except metasomal segments II-V and telson); C, metasomal segments II-V and telson, dorsolateral aspect; D, metasomal segment V and telson, lateral aspect; E, labels. Photos courtesy of Anja Friederichs.

opencc-by-4.0Nov 2011View details →
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Figure 2 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 2: Centruroides margaritatus from Guayaquil (A–B, D, F) and Loja (C, E), Ecuador. A–C, male: A, habitus, dorsal; B– C, telson, lateral aspect. D–F, female: D–E, pedipalp, dorsal aspect; F, metasomal segment V and telson, lateral aspect. Scale (in mm) is only for figure A. Photos C and E, courtesy of J. A. Ochoa Camara.

opencc-by-4.0Nov 2011View details →
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Figure 5 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 5: Centruroides edwardsii. Males from Guanacaste, Costa Rica (A), La Guajira, Colombia (B), Varadero, Matanzas province, Cuba (C), and Durango, Mexico (D). Scale in millimeters only for D.

opencc-by-4.0Nov 2011View details →
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Figure 1 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 1: Centruroides margaritatus. Female holotype. A, dorsal; B, ventral; C, detail of dorsal aspect of carapace; D, last segments of the metasoma and telson, lateral aspect; E, pectines; F, labels. Scale (A, B) = 10 mm. Photos courtesy of E.-A. Leguin.

opencc-by-4.0Nov 2011View details →
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Figure 3 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 3: Geographical distribution of Centruroides edwardsii (black squares) and C. margaritatus (white squares).

opencc-by-4.0Nov 2011View details →
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Figure 4 in On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae)

Figure 4: Centruroides edwardsii. Male neotype. A, carapace and tergites; B, prosoma and mesosoma, ventral aspect; C, right chela, dorsal aspect; D, hand, dorsal aspect; E–H, metasoma: E, segments I–II, dorsal aspect; F, segments I–III, ventral aspect; G, segment V, lateral aspect; H, telson, lateral aspect.

opencc-by-4.0Nov 2011View details →
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Fig. 1. Myxobolus tihanyensis n in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 1. Myxobolus tihanyensis n. sp. plasmodia inhabiting Perca fluviatilis. (A). Plasmodia in the mesenchymal tissue between the caudal fin rays beneath the skin. (B) Plasmodia in the subcutaneous muscle close to the cartilage and ossified caudal fin rays (C) Plasmodia close to the pleural centrum (pc) located in the homocercal caudal fin. (D) Plasmodia is shown in the homocercal caudal skeleton in the urostyle (u) and the hypural (h). Note plasmodia are indicated in black arrows. Scale bars = 500 μm.

opencc-by-4.0Apr 2024View details →
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Fig. 4 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 4. Histology sections of Perca fluviatilis using the haematoxylin and eosin (H & E) technique. (A–B) Sagittal section of the proximal region of the caudal fin. (A) Rounded plasmodia (p) developing in the mesenchyme (mh) closely attached to the bases of the rays (r), scale bar = 100 μm. (B) Higher magnification of plasmodiacontaining spores. Scale bar = 20 μm. (C–D) Transversal section of the caudal vertebrate region. (C) Plasmodia located between the hemal spine (hs) and muscular fibres (mf), scale bar = 200 μm. (D) Higher magnification of plasmodia containing spores (black arrows), scale bar = 20 μm.

opencc-by-4.0Apr 2024View details →
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Fig. 3 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 3. Schematic drawings of the mature spore of Myxobolus tihanyensis n. sp. from the caudal fin of Perca fluviatilis (A) in frontal view, (B) in sutural view. Scale bar = 10 μm.

opencc-by-4.0Apr 2024View details →
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Fig. 2 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 2. Photomicrographs of Myxobolus tihanyensis n. sp. spores from Perca fluviatilis. (A–D) Myxobolus tihanyensis n. sp., and (E–H), Myxobolus sandrae from Sander lucioperca. (A, E) Numerous mature spores (s) illustrate an ovoid shape and two polar capsules (pc). (B, F) Ovoid spores with sutural markings (white arrows) with two polar capsules which contain coiled polar tubules (pf) (C, G) Spore in sutural view showing the suture (su) (D, H) Spores releasing the polar tubules (pf) and showing sutural markings. Figs. C, G and H represented spores stained with Lugol solution. Scale bars = 10 μm.

opencc-by-4.0Apr 2024View details →
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Data from: Strategies of resource sharing in clonal plants: A conceptual model and an example of contrasting strategies in two closely related species

<p>These experimental data were collected to quantify amount of C and N translocated between mother and daughter ramets of two stoloniferous species. Data includes concentrations of 13-C and 15-N in plants samples originating from pulse-chase labelling, absolute amounts of the labels present, as well as dry mass of the samples. Details are described in the relevant paper.</p> <p>&nbsp;</p>

opencc-by-4.0Aug 2024View details →
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Linked collectors and determiners for: Mycophagous gall midges (Diptera, Cecidomyiidae: Lestremiinae, Micromyinae, Winnertziinae, Porricondylinae): first records in Sweden and descriptions of closely related new species from elsewhere.

Natural history specimen data linked to collectors and determiners held within, "Mycophagous gall midges (Diptera, Cecidomyiidae: Lestremiinae, Micromyinae, Winnertziinae, Porricondylinae): first records in Sweden and descriptions of closely related new species from elsewhere". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/6759d43b-e4a5-4743-b3c8-4d0bc3a12d7e">https://bionomia.net/dataset/6759d43b-e4a5-4743-b3c8-4d0bc3a12d7e</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/6759d43b-e4a5-4743-b3c8-4d0bc3a12d7e">https://gbif.org/dataset/6759d43b-e4a5-4743-b3c8-4d0bc3a12d7e</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
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Linked collectors and determiners for: Drosophila (Sophophora) carrolli n. sp., a new species from Brunei, closely related to Drosophila (Sophophora) rhopaloa Bock & Wheeler, 1972 (Diptera: Drosophilidae).

Natural history specimen data linked to collectors and determiners held within, "Drosophila (Sophophora) carrolli n. sp., a new species from Brunei, closely related to Drosophila (Sophophora) rhopaloa Bock &amp; Wheeler, 1972 (Diptera: Drosophilidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/080903f9-fb09-4979-ab23-db718283e177">https://bionomia.net/dataset/080903f9-fb09-4979-ab23-db718283e177</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/080903f9-fb09-4979-ab23-db718283e177">https://gbif.org/dataset/080903f9-fb09-4979-ab23-db718283e177</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View 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