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101 results for “morphological phenotype”

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zenodo32/100

Figure 3 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses

Figure 3. The four states coded in the present study for the shape of the apophyses for the insertion of the stylet muscles (AISM) (characters 14, 15; Table 2). A State 1: AISM divided in two; B AISM shaped as one ridge; C AISM shaped as two ridges; D AISM shaped as three ridges. The images represent half a buccal tube in lateral view. The arrow in B indicates an apophysis for the insertion of the stylet muscles connecting with the end of the mouth. The rest of the apophyses for the insertion of the stylet muscles connect with the beginning of the buccal tube.

opennotspecifiedAug 2013View details →
zenodo32/100

Figure 1 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses

Figure 1. Eutardigrade peribuccal structures indicated by arrows. A, lamellae (state 1 in Tables 3 and 4); B, papulae (state 3 in Tables 3 and 4); C, lobes.

opennotspecifiedAug 2013View details →
zenodo32/100

Figure 7 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses

Figure 7. Agreement subtree with groups present with all concavities obtained with the Ratchet algorithm for parsimonious analyses using combined data: morphological matrix without gamete-related characters and molecular data (18S rRNA and 28S rRNA). Values above branches are bootstrap supports after 1000 replicates with a k-value of 16. Values under branches are Bremer relative supports with a k-value of 16.

opennotspecifiedAug 2013View details →
zenodo32/100

Figure 5. Agreement subtree cladogram obtained with the Ratchet algorithm for parsimonious analyses using the complete morphological matrix without gamete-related characters. Values above branches are bootstrap supports after 1000 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses

Figure 5. Agreement subtree cladogram obtained with the Ratchet algorithm for parsimonious analyses using the complete morphological matrix without gamete-related characters. Values above branches are bootstrap supports after 1000 replicates; values under branches are Bremer relative supports.

opennotspecifiedAug 2013View details →
zenodo32/100

Figure 2 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses

Figure 2. Different states (from 0 to 5) coded in the present study for the shape of the furcae (character 13; Table 2).

opennotspecifiedAug 2013View details →
zenodo32/100

Figure 4 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses

Figure 4. Different types of claws present amongst eutardigrades (A–N) and in the outgroup Echiniscidae (O). M modified from Pilato (1971). Dotted lines in F and G indicate right angles in Isohypsibius- and Hypsibius-type claws, respectively. Arrows in D and E indicate cuticular bars joining external and internal claws in Dactylobiotus and Macroversum, respectively. Arrows in L indicate claw position. PIII, third pair of legs. PIV, fourth pair of legs.

opennotspecifiedAug 2013View details →
ClinicalTrials.gov32/100

The Role of Morphological Phenotype in ARDS

ClinicalTrials.gov study NCT04157946. IPD Sharing: NO. Countries: 1. Publications: 8.

closedIPD-NOFeb 2026View details →
dryad32/100

Data from: Intraspecific phenotypic variation and morphological divergence of strains of Folsomia candida (Willem) (Collembola: Isotomidae), the "standard" test springtail

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publicAug 2016View details →
dryad32/100

Data from: Phenotypic plasticity in the mandibular morphology of Japanese macaques: captive–wild comparison

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publicMay 2019View details →
dryad32/100

Data from: Morphological change and phenotypic plasticity in native and non–native pumpkinseed sunfish in response to sustained water velocities

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publicOct 2013View details →
dryad32/100

Data from: Niche theory and its relation to morphology and phenotype in geographic space: a case study in woodpeckers (Picidae)

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publicSep 2018View details →
dryad32/100

Data from: Physical and physiological impacts of ocean warming alter phenotypic selection on sperm morphology

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publicNov 2019View details →
dryad32/100

Data from: Evidence of phenotypic plasticity of penis morphology and delayed reproductive maturation in response to male competition in waterfowl

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publicAug 2018View details →
dryad32/100

Data from: Morphological novelty emerges from pre-existing phenotypic plasticity

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publicJun 2019View details →
dryad32/100

Phenotypic assortment by morphology in social partners of the forked fungus beetle Bolitotherus cornutus

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publicDec 2021View details →
zenodo28/100

Fig. 8 in Cranial phenotypic variation in Meriones crassus and M. libycus (Rodentia, Gerbillinae), and a morphological divergence in M. crassus from the Iranian Plateau and Mesopotamia (Western Zagros Mountains)

Fig. 8. Dendograms obtained from the (A) NJ clustering and (B) UPGMA, using Euclidean distances between group means by combining all data (shape information from dorsal, ventral and lateral views). Branch bootstrap support shown at the nodes, 10 000 replicates.

opencc-by-3.0Jun 2014View details →
zenodo28/100

Fig. 2 in Cranial phenotypic variation in Meriones crassus and M. libycus (Rodentia, Gerbillinae), and a morphological divergence in M. crassus from the Iranian Plateau and Mesopotamia (Western Zagros Mountains)

Fig. 2. Landmarks positioned on the cranium of Meriones crassus Sundevall, 1842 shown in (A) ventral (B) dorsal and (C) lateral views. The straight lines on the ventral and lateral views were used for defining semi-landmarks based on two other landmarks. Open circles on the ventral side: the most rostral and on the most caudal point of the tympanic bulla, and on the lateral side: the most rostral margin of the tympanic bulla. Short lines are drawn to highlight sutures which are unclear here and on which the landmarks have been defined.

opencc-by-3.0Jun 2014View details →
zenodo28/100

Fig. 5 in Cranial phenotypic variation in Meriones crassus and M. libycus (Rodentia, Gerbillinae), and a morphological divergence in M. crassus from the Iranian Plateau and Mesopotamia (Western Zagros Mountains)

Fig. 5. Box-and-whisker plots of (A) skull size and (B) relative bulla size of the ventral cranium. The boxes indicate the 25–75 % quartiles; the whiskers represent the minimal and maximal values.

opencc-by-3.0Jun 2014View details →
dryad28/100

Phylogeographic analysis of character displacement in feeding phenotypes of snail-feeding Acoptolabrus ground beetles: Morphological measurements

<p>Ecological character displacement predicts that interspecific resource competition results in greater trait divergence between species in sympatry than in allopatry. In this study, we characterize character displacement in 8 species of snail-feeding <i>Acoptolabrus</i> ground beetles (Coleoptera, Carabidae, genus <em>Carabus</em>) in the Far East. <i>Acoptolabrus</i> exhibit divergent feeding phenotypes, including species with a slender forebody for intruding large shells and species with stout heads and mandibles for crushing small shells. Distance measurements (in mm) deposited here are for evaluating body shape variation among 8 <em>Acoptolabrus</em> species.</p>

opencc-zeroAug 2020View details →
dryad28/100

Data from: Toward synthesizing our knowledge of morphology: using ontologies and machine reasoning to extract presence/absence evolutionary phenotypes across studies

The reality of larger and larger molecular databases and the need to integrate data scalably have presented a major challenge for the use of phenotypic data. Morphology is currently primarily described in discrete publications, entrenched in noncomputer readable text, and requires enormous investments of time and resources to integrate across large numbers of taxa and studies. Here we present a new methodology, using ontology-based reasoning systems working with the Phenoscape Knowledgebase (KB; kb.phenoscape.org), to automatically integrate large amounts of evolutionary character state descriptions into a synthetic character matrix of neomorphic (presence/absence) data. Using the KB, which includes more than 55 studies of sarcopterygian taxa, we generated a synthetic supermatrix of 639 variable characters scored for 1051 taxa, resulting in over 145,000 populated cells. Of these characters, over 76% were made variable through the addition of inferred presence/absence states derived by machine reasoning over the formal semantics of the source ontologies. Inferred data reduced the missing data in the variable character-subset from 98.5% to 78.2%. Machine reasoning also enables the isolation of conflicts in the data, that is, cells where both presence and absence are indicated; reports regarding conflicting data provenance can be generated automatically. Further, reasoning enables quantification and new visualizations of the data, here for example, allowing identification of character space that has been undersampled across the fin-to-limb transition. The approach and methods demonstrated here to compute synthetic presence/absence supermatrices are applicable to any taxonomic and phenotypic slice across the tree of life, providing the data are semantically annotated. Because such data can also be linked to model organism genetics through computational scoring of phenotypic similarity, they open a rich set of future research questions into phenotype-to-genome relationships.

opencc-zeroDec 2014View 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