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153 results for “Ecological biogeography”

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dryad32/100

Data from: Ecology, biofacies, biogeography and systematics of micromorphic lingulate brachiopods from the Ordovician (Darriwilian–Sandbian) of south-central China

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publicFeb 2018View details →
dryad32/100

Phylogenomics, biogeography, and evolution of morphology and ecological niche of the eastern Asian‐ eastern North American Nyssa (Nyssaceae)

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publicMay 2020View details →
dryad32/100

Data from: Biogeography of scorpions in the Pseudouroctonus minimus complex (Vaejovidae) from south-western North America: implications of ecological specialization for pre-Quaternary diversification

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publicJun 2013View details →
dryad32/100

Biogeography and ecological niche evolution in Diapensiaceae inferred from phylogenetic analysis

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publicJul 2022View details →
dryad32/100

Data from: SpeciesGeoCoder: fast categorization of species occurrences for analyses of biodiversity, biogeography, ecology and evolution

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publicJul 2016View details →
zenodo28/100

FIGURE 6 in Simuliidae (Diptera) of the Solomon Islands: new records and species, ecology, and biogeography

FIGURE 6. Simulium (G.) sherwoodi, Guadalcanal. Pupal gill, thoracic cuticle, and antennal sheath.

opennotspecifiedDec 2006View details →
zenodo28/100

FIGURE 16. F. smiti larva A in The intertidal Fortuyniidae (Acari: Oribatida): new species, morphological diversity, ecology and biogeography

FIGURE 16. F. smiti larva A) dorsal view. B) ventral view.

opennotspecifiedDec 2015View details →
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FIGURE 15. F. smiti adult left legs, antiaxial view. A in The intertidal Fortuyniidae (Acari: Oribatida): new species, morphological diversity, ecology and biogeography

FIGURE 15. F. smiti adult left legs, antiaxial view. A) leg I. B) leg II. C) leg III. D) leg IV.

opennotspecifiedDec 2015View details →
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FIGURE 14. Fortuynia smiti adult. A in The intertidal Fortuyniidae (Acari: Oribatida): new species, morphological diversity, ecology and biogeography

FIGURE 14. Fortuynia smiti adult. A) dorsal view. B) ventral view. C) lateral view.

opennotspecifiedDec 2015View details →
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FIGURE 2. F in The intertidal Fortuyniidae (Acari: Oribatida): new species, morphological diversity, ecology and biogeography

FIGURE 2. F. maledivensis sp. nov. adult. A) dorsal view. B) ventral view. C) lateral view.

opennotspecifiedDec 2015View details →
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FIGURE 7 in The intertidal Fortuyniidae (Acari: Oribatida): new species, morphological diversity, ecology and biogeography

FIGURE 7. Fortuynia longiseta sp. nov. adult. A) dorsal view. B) ventral view. C) lateral view.

opennotspecifiedDec 2015View details →
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FIGURE 13. A in The intertidal Fortuyniidae (Acari: Oribatida): new species, morphological diversity, ecology and biogeography

FIGURE 13. A. pseudoreticulatus sp. nov. tritonymph. A) dorsal view. B) ventral view.

opennotspecifiedDec 2015View details →
zenodo28/100

Figure 7 in Is mimicry a diversification-driver in ants? Biogeography, ecology, ethology, genetics and morphology define a second West-Palaearctic Colobopsis species (Hymenoptera: Formicidae)

Figure 7. Coexistence between Colobopsis and their putative model species on the same tree.

opennotspecifiedJul 2021View details →
zenodo28/100

FIGURE 1 in Tooth enamel microstructure in North American Phytosauria (Diapsida:Archosauriformes): Implications for biogeography and ecology of a Late Triassic clade of crocodylian-like predators

FIGURE 1. Geographic distribution and phylogenetic position of phytosaurs. 1A—Global distribution of phytosaur specimens from Middle and Late Triassic modified from Stocker and Butler (2013). Palaeomap from C. Scotese built into the Paleobiology Database for the Late Triassic (220 Ma) 1B—General cladogram of archosauromorphs that have been sampled for EM with the two possible positions of Phytosauria marked in red. Based on Heckert and Miller-Camp (2012) 1C—Locality map of specimens used in this study. North Carolina not to the same scale as western states. Locality numbers from NMMNH (western states) or NCSM (North Carolina).

opencc-by-4.0Dec 2021View details →
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FIGURE 2 in Tooth enamel microstructure in North American Phytosauria (Diapsida:Archosauriformes): Implications for biogeography and ecology of a Late Triassic clade of crocodylian-like predators

FIGURE 2. Classification and measurement of the teeth sampled here. 2A—Idealized drawings of heterodont phytosaur teeth following Hunt (1989; type C, U, I, B), Hungerbühler (2001; tip-of-snout, premaxillary, maxillary), and Datta et al. (2021; morphotypes IA, IB, IC, ID). 2B—Schematic of macro-morphological measurements taken on phytosaur teeth as preservation allowed. Measurements following the protocols of Smith (2005) with purple labels: CH—crown height, CBL—crown base length, AL—apical length, CA—crown angle (angle GAB), MA—mesial apical, MC—mesial mid-crown, and MB—mesial basal denticle densities, DA—distal apical, DC—distal mid-crown, and DB—distal basal denticle densities, with measurements new to this study in green: LAH—labial height, LIH—lingual height, and LLA— labio-lingual angle.

opencc-by-4.0Dec 2021View details →
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FIGURE 9 in Tooth enamel microstructure in North American Phytosauria (Diapsida:Archosauriformes): Implications for biogeography and ecology of a Late Triassic clade of crocodylian-like predators

FIGURE 9. Boxplots of overall enamel thickness and enamel thickness to crown height ratio. Circles around boxplots represent outliers. 9A—Enamel thickness (μm) by tooth type. Type B teeth have the thickest enamel on average; 9B— Enamel thickness (μm) over crown height (mm) by tooth type. We included this ratio as a way to account for the overall size of teeth. Type B teeth have the thickest enamel on average, followed by type U; 9C—Enamel thickness (μm) of transverse sections by taxonomic assignment with stratigraphically oldest on the left of the plot,showing variation in enamel thickness but no chronological trend; 9D—Enamel thickness (μm) of transverse sections of type I teeth. When only considering type I teeth enamel thickness thins through time; 9E—Enamel thickness (μm) over crown height (mm) of transverse sections of type I teeth. When overall tooth size is accounted for, the opposite of Figure 9E is seen with typical enamel per mm height increasing through time.

opencc-by-4.0Dec 2021View details →
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FIGURE 3 in Tooth enamel microstructure in North American Phytosauria (Diapsida:Archosauriformes): Implications for biogeography and ecology of a Late Triassic clade of crocodylian-like predators

FIGURE 3. Generalized stratigraphic distribution of the phytosaur teeth sampled here (L-3380, L-3845, L-4211, L- 6818, NCPALEO1902) and by Sander (1999; IPB E-2011, 2007I-III) compared to stratigraphic distribution of heterodont phytosaurs, North American biostratigraphy, and the standard global chronostratigraphic scale (SGCS). See text for details of the stratigraphy of each locality. Numerical age estimates draw on a variety of sources, including Heckert et al., 2009; Irmis et al., 2011; Ramezani et al., 2011; Whiteside et al., 2011. FAD = First appearance datum; L- = locality numbers for New Mexico Museum of Natural History and Science; LVF = Land-vertebrate faunachron (= "holochron"); NCPaleo = Locality for North Carolina Museum of Natural Sciences.

opencc-by-4.0Dec 2021View details →
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FIGURE 8 in Tooth enamel microstructure in North American Phytosauria (Diapsida:Archosauriformes): Implications for biogeography and ecology of a Late Triassic clade of crocodylian-like predators

FIGURE 8. SEM captures of Redondasaurus teeth from the Redonda Formation of New Mexico. 8A—NMMNH P- 36184 type I tooth in transverse section with poorly-developed LIGs near OES as well as a few more near the center; 8B—NMMNH P-36185 type I tooth in transverse section with well-developed columns along lingual margin; 8C— NMMNH P-36186 type B tooth in transverse section along labial margin; 8D—NMMNH P-36186 type B tooth in transverse section along lingual margin; 8E—NMMNH P-36186 type B tooth in transverse section with well-developed columns; 8F—NMMNH P-36186 type B tooth in tangential section with ~50 µm at bottom of enamel, just above enameldentine junction (EDJ) showing polygonal columnar packages. All scale bars equal 50 µm.

opencc-by-4.0Dec 2021View details →
zenodo28/100

Figure 2 from: Jażdżewska AM, Corbari L, Driskell A, Frutos I, Havermans C, Hendrycks E, Hughes L, Lörz A-N, Stransky B, Tandberg AHS, Vader W, Brix S (2018) A genetic fingerprint of Amphipoda from Icelandic waters – the baseline for further biodiversity and biogeography studies. In: Brix S, Lörz A-N, Stransky B, Svavarsson J (Eds) Amphipoda from the IceAGE-project (Icelandic marine Animals: Genetics and Ecology). ZooKeys 731: 55–73. https://doi.org/10.3897/zookeys.731.19931

Figure 2 Neighbour-joining (NJ) tree of COI sequences (Suppl. material 1) based on Kimura 2-parameter. Triangles indicate the relative number of individuals studied (height) and sequence divergence (width). The asterisk (*) symbolizes taxa having already published sequences in BOLD/GenBank identified to species level. The numbers in front of the nodes indicate bootstrap support (1000 replicates, only values higher than 50% are presented). The vertical bars represent species delimitations taxonomies obtained from morphology and different species delimitation methods. The same colour indicates the same nominal species. Only the cases where incongruence between different delimitation methods were observed are shown. Note that this tree is not the reconstruction of evolutionary history of presented taxa.

opencc-by-4.0Feb 2018View details →
zenodo28/100

Figure 1 from: Jażdżewska AM, Corbari L, Driskell A, Frutos I, Havermans C, Hendrycks E, Hughes L, Lörz A-N, Stransky B, Tandberg AHS, Vader W, Brix S (2018) A genetic fingerprint of Amphipoda from Icelandic waters – the baseline for further biodiversity and biogeography studies. In: Brix S, Lörz A-N, Stransky B, Svavarsson J (Eds) Amphipoda from the IceAGE-project (Icelandic marine Animals: Genetics and Ecology). ZooKeys 731: 55–73. https://doi.org/10.3897/zookeys.731.19931

Figure 1 Sampling stations. Depth contours are the following: 500 m, 1000 m, 1500 m, 2000 m, 2500 m, 3000 m. Station details are in Suppl. material 1.

opencc-by-4.0Feb 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