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1,154 results for “Extant”

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Figure 1. A in How long can insect species exist? Evidence from extant and fossil Micromalthus beetles (Insecta: Coleoptera)

Figure 1. A, photograph of Micromalthus debilis in Dominican amber (MTEC226, MSU Bozeman, USA), female specimen. B, extant female M. debilis in dorsal view. The abdomen appears comparatively short in the extant specimen because of (1) perspective distortion because the abdomen is bent downward and (2) because the segments are retracted. Arrows mark the protruding edges of two segments; in (A) the segments are fully extended.

opennotspecifiedOct 2009View details →
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Figure 3. A–C in How long can insect species exist? Evidence from extant and fossil Micromalthus beetles (Insecta: Coleoptera)

Figure 3. A–C, photographs of heads of Dominican amber specimens of Micromalthus from the Poinar collection. A, coll.no. C 7-191°.B, coll.no. C 7-191B. C, coll.no. C 7-191C. D, scanning electron micrograph of left antenna of extant specimen of Micromalthus debilis, dorsal view.

opennotspecifiedOct 2009View details →
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Figure 2 in How long can insect species exist? Evidence from extant and fossil Micromalthus beetles (Insecta: Coleoptera)

Figure 2. Micromalthus debilis from Dominican amber (MTEC226 MTU Bozeman, USA). A, dorsal view. B, ventral view, wings omitted, mouthparts and mesothorax obscured by white, foggy substance. A cloud of this substance also surrounds the last three abdominal segments. C, reconstruction of wing venation of fossil specimen. Nomenclature of wing veins after Wallace & Fox (1975). Scale bars = 0.5 mm.

opennotspecifiedOct 2009View details →
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Figure 25 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 25. Ordinary least-square (OLS) regressions between standardized contrasts in the ratios of maximum prey weight (MPW)/cat average weight and the positivized standardized contrasts in bite force. Plots indicate the nodes and lineages of the phylogeny. Nodes connecting different cat lineages are indicated by the age of cladogenesis (Myr), according the cladogram of Johnson et al. (2006) presented in Figure 1.

opennotspecifiedOct 2010View details →
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Figure 18 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 18. Morphofunctional relationships between the members of the leopard cat lineage. Species' images are digitally adjusted and scaled according to the skull of Prionailurus viverrinus, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate bite force and neck robustness (abscissa), and jaw muscle optimization (ordinate). Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 11 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 11. Morphological relationships between the members of the bay cat lineage. Species' images are digitally adjusted and scaled according to the skull of Catopuma temminckii, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 2. Diagram showing the 20 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 2. Diagram showing the 20 skull measurements used in the analysis (see Appendix 1 for definitions).

opennotspecifiedOct 2010View details →
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Figure 1 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 1. Cladogram of the family Felidae, after Johnson et al. 's (2006) phylogeny, adjusted to the number of species analysed. Values on the branches indicate the divergence time between nodes; node numbers are parenthetic.

opennotspecifiedOct 2010View details →
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Figure 7 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 7. Morphological relationships between the members of the Ocelot lineage. Species' images are digitally adjusted and scaled according the skull of Leopardus pardalis, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 4 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 4. Morphological relationships between the members of the Panthera lineage. Species' images are digitally adjusted and scaled according to the skull of Panthera leo, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 3 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 3. Distribution of the 34 cat species, according to their scores from the morphological principal component analysis (PCA). Plots represent species' centroids based on bivariate means of the scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 6 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 6. Morphological relationships between the members of the Lynx lineage. Species' images are digitally adjusted and scaled according the skull of Lynx lynx, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 14 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 14. Morphofunctional relationships between the members of the Puma lineage. Species' images are digitally adjusted and scaled according to the skull of Puma concolor, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate bite force and neck robustness (abscissa), and jaw muscle optimization (ordinate). Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 13 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 13. Morphofunctional relationships between the members of the Panthera lineage. Species' images are digitally adjusted and scaled according to the skull of Panthera leo, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate bite force and neck robustness (abscissa), and jaw muscle optimization (ordinate). Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 16 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 16. Morphofunctional relationships between the members of the Ocelot lineage. Species' images are digitally adjusted and scaled according to the skull of Leopardus pardalis, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate bite force and neck robustness (abscissa), and jaw muscle optimization (ordinate). Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 20 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 20. Morphofunctional relationships between the members of the bay cat lineage. Species' images are digitally adjusted and scaled according to the skull of Catopuma temminckii, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate bite force and neck robustness (abscissa), and jaw muscle optimization (ordinate). Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 10 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 10. Morphological relationships between the members of the Caracal lineage. Species' images are digitally adjusted and scaled according to the skull of Profelis aurata, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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Figure 9 in Skull morphology and functionality of extant Felidae (Mammalia: Carnivora): a phylogenetic and evolutionary perspective

Figure 9. Morphological relationships between the members of the leopard cat lineage. Species' images are digitally adjusted and scaled according to the skull of Prionailurus viverrinus, and are positioned over the centroids of their principal component analysis (PCA) scores. Arrows indicate the enlargement of the skull measurements related to each axis. Acronyms are defined in the text.

opennotspecifiedOct 2010View details →
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FIGURES 36–43 in Revision of the genus Lopesiodinia Prado, 1973 (Diptera: Odiniidae) with description of three new species, and a key to the extant Neotropical genera and species of Traginopinae

FIGURES 36–43. Lopesiodinia pontarolloi, sp. nov. Figs 36–39, paratype ♂. Figs 40–43, paratype ♀. 36–39, terminalia male, dorsal, posterior, lateral and ventral views, respectively; 40–42, terminalia female, lateral, dorsal and ventral views, respectively; 43, spermathecae.

opennotspecifiedOct 2021View details →
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FIGURES 22–29 in Revision of the genus Lopesiodinia Prado, 1973 (Diptera: Odiniidae) with description of three new species, and a key to the extant Neotropical genera and species of Traginopinae

FIGURES 22–29. Lopesiodinia argentata, sp. nov. Figs 22–25, holotype ♂. Figs 26–29, paratype ♀. 22–25, terminalia male, dorsal, posterior, lateral and ventral views, respectively; 26–28, terminalia female, lateral, dorsal and ventral views, respectively; 29, spermathecae.

opennotspecifiedOct 2021View 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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