Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
54
datasets available to search
ShareScore release 0.9.0
Dataset results
54 results for “colour morphs”
Figure 2 in Species status of two colour morphs of Eupelmus vesicularis (Hymenoptera: Eupelmidae) as revealed by allozyme electrophoresis, morphometric and host preference data
Figure 2. Scaterplots of pairs of variables for Eupelmus vesicularis light colour and dark colour forms. Note: All measurements in mm.
Figure 4 in Species status of two colour morphs of Eupelmus vesicularis (Hymenoptera: Eupelmidae) as revealed by allozyme electrophoresis, morphometric and host preference data
Figure 4. Enzyme electromorphs of Eupelmus vesicularis light colour form (left) and dark colour form (right). Notes: The direction of current flow is indicated by +; the specimen loading point is shown by an arrow.
Figure 3 in Species status of two colour morphs of Eupelmus vesicularis (Hymenoptera: Eupelmidae) as revealed by allozyme electrophoresis, morphometric and host preference data
Figure 3. Plot of the first two factors from the principal component analysis of the log-transformed raw measurements.
Figure 1 in Species status of two colour morphs of Eupelmus vesicularis (Hymenoptera: Eupelmidae) as revealed by allozyme electrophoresis, morphometric and host preference data
Figure 1. Measurements of forewing rudiment and hind tibia for morphometric analysis of Eupelmus vesicularis (female). Notes: ti3L, hind tibia length; waL, forewing apical part length; wbL, forewing base length.
Figure 2 in Allozyme comparison of the species and colour morphs of the nemertean genus Quasitetrastemma Chernyshev, 2004 (Hoplonemertea: Tetrastemmatidae) from the Sea of Japan
Figure 2. Quasitetrastemma stimpsoni and colour morphs of Quasitetrastemma nigrifrons (A) var. spadix, (B) var. bilineatum, (C) var. aequicolor, (D) Q. stimpsoni, (E–H) var. palllidum (E–G, pallidum 1, H, pallidum 2). Scale bar 5 mm.
Figure 3 in Allozyme comparison of the species and colour morphs of the nemertean genus Quasitetrastemma Chernyshev, 2004 (Hoplonemertea: Tetrastemmatidae) from the Sea of Japan
Figure 3. The UPGMA phenogram, representing Nei's (1978) genetic similarity among Quasitetrastemma species.
Figure 1. A in Allozyme comparison of the species and colour morphs of the nemertean genus Quasitetrastemma Chernyshev, 2004 (Hoplonemertea: Tetrastemmatidae) from the Sea of Japan
Figure 1. A schematic representation of the colour morphs of (A–L) Quasitetrastemma nigrifrons: (A) var. spadix, (B) var. bicolor, (C, D) var. bilineatum, (E) var. bimaculatum, (F) var. aequicolor, (G–L) var. pallidum; and (M) Quasitetrastemma stimpsoni.
FIGURE 3 in Sexual morphs and colour variants of Aphis (formerly Toxoptera) odinae (Hemiptera, Aphididae) in Japan
FIGURE 3. Plot of the mean scores on the first two canonical variates (CVs) of 23 samples of A. odinae: a, labelled according to the host plants on which they were collected; b, labelled according to their countries of origin and colour.
FIGURE 2 in Sexual morphs and colour variants of Aphis (formerly Toxoptera) odinae (Hemiptera, Aphididae) in Japan
FIGURE 2. Colour photographs of living A. odinae: a, fundatrix with bluish black progeny; b, fundatrix with brown progeny; c, oviparae and male; d, apterous viviparae of brown form (photograph by courtesy of Dr Poorani Janakiraman); e, apterous vivipara of green form; f, colony with mixture of the two colour forms.
Great tit predation on colour morphs of the wood tiger moth at different relative frequencies
<p>Polymorphic warning signals in aposematic systems are enigmatic because predator learning should favor the most common form, creating positive frequency-dependent survival. However, many populations exhibit variation in warning signals. There are various selective mechanisms which can counter positive frequency-dependent selection and lead to temporal or spatial warning signal diversification. Examining these mechanisms and their effects requires first confirming whether the most common morphs are favored at both local and regional scales. Empirical examples of this are uncommon and often include potentially confounding factors such as a lack of knowledge of predator identity and behavior. We tested how bird behavior influences the survival of three coexisting morphs of the aposematic wood tiger moth <i>Arctia plantaginis </i>offered to a sympatric predator (great tits, <i>Parus major</i>) at different frequencies.<i> </i>We found that although positive frequency-dependent selection is present, its strength is affected by predator characteristics and varying prey profitability. These results highlight the need to understand predator foraging in natural communities with variable prey defences, in order to better examine how behavioral interactions shape evolutionary outcomes.</p>
Data from: Heterospecific aggression bias towards a rarer colour morph
Open the record for dataset details and reuse information.
Data from: Discrete colour polymorphism in the tawny dragon lizard (Ctenophorus decresii) and differences in signal conspicuousness among morphs
Open the record for dataset details and reuse information.
Data from: Intensity of male-male competition predicts morph diversity in a colour polymorphic lizard
Open the record for dataset details and reuse information.
Data from: The many faced symbiotic snakelocks anemone (Anemonia viridis, Anthozoa): host and symbiont genetic differentiation among colour morphs
Open the record for dataset details and reuse information.
Data from: The colour of paternity: extra-pair paternity in the wild Gouldian finch does not appear to be driven by genetic incompatibility between morphs
Open the record for dataset details and reuse information.
Data from: AFLP genome scans suggest divergent selection on colour patterning in allopatric colour morphs of a cichlid fish
Open the record for dataset details and reuse information.
Data from: Significant differences in maternal carotenoid provisioning and effects on offspring fitness in Chinook salmon colour morphs
Open the record for dataset details and reuse information.
Data from: Phylogeographic structure, demographic history, and morph composition in a colour polymorphic lizard
Open the record for dataset details and reuse information.
Data from: Rapid, habitat-related evolution of land snail colour morphs on reclaimed land
Open the record for dataset details and reuse information.
Data from: Morphological and colour morph clines along an altitudinal gradient in the meadow grasshopper Pseudochorthippus parallelus
Open the record for dataset details and reuse information.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.
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.
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.
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.
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.