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1,104 results for “morphological variation”

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dryad36/100

Morphometric and phylogeny data for: Morphology, variation, and systematics of the late Cambrian Laurentian dikelocephalid trilobite Walcottaspis vanhornei

<p></p> <p><span>These pages provide details of the taxa, characters and character states used in the phylogenetic analyses of <em>Walcottaspis vanhornei </em></span><span>(Walcott, 1914)</span><span> </span><span>and relatives in the accompanying paper. <span> </span>Phylogenetic information included here provides details of characters and taxa used for both the parsimony-based and Bayesian analyses and documents levels of support of two types (Bremer and bootstrap) for the parsimony analysis. Also included here is the result of Bayesian maximum likelihood analysis that provides further support to the results of parsimony analysis. We include bivariate plots of the variance explained by each relative warp for the sclerites analyzed and morphometric measurement error analysis. </span></p>

opencc-zeroApr 2023View details →
dryad36/100

Patterns of genetic variation and morphology support the recognition of five species in the Gaultheria leucocarpa Blume (Ericaceae) group from mainland China

<p><em>Gaultheria</em> <em>leucocarpa</em> and its varieties form a clade of aromatic shrubs that is widely distributed in subtropical and East Asian tropical regions. The group is taxonomically difficult and is in need of thorough taxonomic investigation. This study focused on taxonomic delimitation within the <em>G. leucocarpa </em>group from mainland China. Field surveys covering the distributional range of <em>G. leucocarpa</em> in mainland China were conducted, wherein four populations from Yunnan and one from Hunan were found bearing visibly morphological and habitat differences. A 63-species phylogenetic tree of <em>Gaultheria</em> based on one nuclear and three chloroplast markers that included samples from the <em>G. leucocarpa</em> group was reconstructed with maximum likelihood to clarify the monophyly of the <em>G. leucocarpa</em> group. Taxonomic relationships among populations of the <em>G. leucocarpa</em> group were investigated with morphology and population genetics, the latter by using two chloroplast genes and two low-copy nuclear genes. Based on the sum of morphological and genetic analyses, we described three species of <em>Gaultheria</em> as new to science, clarified the taxonomic status of <em>G. leucocarpa</em> var. <em>pingbienensis</em>, elevating it to the species level, and resurrected <em>G</em>. <em>crenulata</em> and treated the varieties <em>G. leucocarpa </em>var<em>. crenulata</em>, and <em>G. leucocarpa </em>var<em>. yunnanensis</em> as synonyms of this species. We provide a key to the five species now recognized, along with descriptions and photographs.</p>

opencc-zeroMay 2023View details →
zenodo36/100

Figure 7 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations

Figure 7. Phaea quadrimaculata Wappes &amp; Santos-Silva, 2020. (A-E) Male from Mexico, Oaxaca: (A) Dorsal habitus; (B) Ventral habitus; (C) Abdominal ventrites; (D) Lateral habitus; (E) Head, frontal view. (F) Holotype female, abdominal ventrites.

opencc-by-nc-4.0Jul 2023View details →
zenodo36/100

Figure 1 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations

Figure 1. Xystochroma luteotarsis sp. nov. (A-E) Holotype male: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view; (E) Scape. (F-G) Paratype female: (F) Dorsal habitus; (G) Ventral habitus.

opencc-by-nc-4.0Jul 2023View details →
zenodo36/100

Figure 4 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations

Figure 4. Rosalba strandi (Breuning, 1943). (A-D) Male, specimen 1, from Paraguay: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view. (E) Male from Brazil (Minas Gerais, Serra do Caraça), dorsal habitus. (F-G) Female from Paraguay: (F) Dorsal habitus; (G) Ventral habitus. (H-J) Males from Paraguay, dorsal habitus: (H) specimen 2; (I) specimen 3; (J) specimen 4.

opencc-by-nc-4.0Jul 2023View details →
zenodo36/100

Figure 3 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations

Figure 3. Bisaltes (Bisaltes) lateralis sp. nov., holotype female: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view; (E) Scape.

opencc-by-nc-4.0Jul 2023View details →
zenodo36/100

Figure 2 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations

Figure 2. Psyrassa spp. (A-F) P. tysoni sp. nov., holotype female: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view; (E) Head, lateral view; (F) Procoxal cavities. (G-J) P. pertenuis (Casey, 1924), holotype: (G) Lateroventral view; (H) Dorsal habitus; (I) Head, frontal view; (J) Partial lateral habitus. Figures G, I, and J by Eugenio H. Nearns; figure H from Lingafelter et al. (2023).

opencc-by-nc-4.0Jul 2023View details →
dryad36/100

Genetic and morphological data from two bird genera (Cranioleuca and Geospiza) showing continuous variation

<p class="MsoNormal">Extinction is a dominant force shaping patterns of biodiversity through time however its role as a catalyst of speciation has been overlooked. Here, we synthesize ideas alluded to by Darwin and others into the model of 'speciation-by-extinction' in which speciation results from the extinction of intermediate populations within a single geographically variable species. We explore the properties and distinguishing features of speciation-by-extinction with respect to other established speciation models. We demonstrate its plausibility by showing that the experimental extinction of populations within variable species can result in speciation. The prerequisites for speciation-by-extinction, geographically structured intraspecific variation and local extinction, are ubiquitous in nature, indicating that speciation-by-extinction may be a prevalent, but underappreciated, speciation mechanism.</p>

opencc-zeroJul 2023View details →
dryad36/100

Intrasexual variations in arm morphology related to alternative reproductive tactics in Japanese spear squid

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publicDec 2024View details →
dryad36/100

Geometric morphometrics as a tool for evaluating Eublastoidea morphological variation

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publicMar 2024View details →
dryad36/100

Data from: Sugar-rich resources mediate geographic morphological variation in a dominant, neotropical savanna ant

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publicApr 2025View details →
dryad36/100

Data from: Seasonality and morphological variation shape intraspecific seed dispersal networks in gopher tortoises

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publicSep 2025View details →
dryad36/100

Genetic variation of morphological scaling in Drosophila

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publicNov 2022View details →
dryad36/100

A colonial epiphyte with a twist: Morphological variation and potential division of labour in the fern <em>Platycerium bifurcatum</em>

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publicSep 2025View details →
dryad36/100

Patterns of genetic variation and morphology support the recognition of five species in the Gaultheria leucocarpa Blume (Ericaceae) group from mainland China

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publicMay 2023View details →
dryad36/100

Variation in mouse pelvic morphology maps to locations enriched in Sox9 Class II and Pitx1 regulatory features

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publicFeb 2020View details →
dryad36/100

Concordant patterns of morphological, stable isotope, and genetic variation in a recent ecological radiation (Salmonidae:Coregonus spp.)

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publicMay 2022View details →
dryad36/100

Ecologically-related variation of digit morphology in Cyrtodactylus (Gekkota, Squamata) reveals repeated origins of incipient adhesive toepads

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publicMay 2024View details →
dryad36/100

Ecological variation drives morphological differentiation in a highly social vertebrate

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publicJun 2021View details →
dryad36/100

Broad- and small-scale environmental gradients drive variation in chemical, but not morphological, leaf traits of vascular epiphytes

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publicMay 2022View 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