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40 results for “Selective constraint”

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zenodo40/100

Fig. 5. Selected gastropods from the Goychay section. A in Magneto-biostratigraphic age constraints on the palaeoenvironmental evolution of the South Caspian basin during the Early-Middle Pleistocene (Kura basin, Azerbaijan)

Fig. 5. Selected gastropods from the Goychay section. A. Theodoxus pallasi; B. Theodoxus pallasi; C. Laevicaspia sp. D. Laevicaspia subcaspia; E. Caspia apsheronica; F. Caspia sp.; G. Clessiniola cf. subvariabilis; H. Ecrobia cf. grimmi; I. Laevicaspia subcaspia; J. Melanopsis bergeroni; K. Lymnaea sp.; L. Turricaspia sp.; M. Laevicaspia sp.; N. Streptocerella sp.; O. Gyraulus sp.; P. Valvata sp. (Scale bars 1 mm).

opencc-by-4.0Oct 2019View details →
dryad40/100

Data from: Selection and constraints in the ecomorphological adaptive evolution of the skull of living Canidae (Carnivora, Mammalia)

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publicMar 2020View details →
dryad36/100

The stabilising impact of natural selection on the allometry of sexual ornaments: Fish that escape locomotor constraints exhibit extravagant ornamentation

<p>1. Positive allometry has been considered a hallmark of sexual selection whereby larger males of superior condition develop disproportionately larger ornaments for their body size compared to smaller males of poorer condition.</p> <p>2. Yet many structures known to be sexually selected often exhibit other allometric patterns. This has led to controversy over the utility of allometry in adequately capturing the signature of sexual selection, particularly if static (within population) and evolutionary (across species) allometries are functionally constrained by stabilising natural selection.</p> <p>3. To investigate this, we evaluated the allometries of ornamental head crests and dorsal fins across multiple species of blenny fish. In particular, we compared species that occupied an aquatic environment—where swimming performance was expected to have constrained ornament size—with species that have transitioned onto land where such biomechanical constraints on ornament size have been removed.</p> <p>4. Static allometries of both head crest and dorsal fin ornaments were found to be positive in males, but less so in females, across all species examined. This was consistent with the allometric theory of sexual selection that predicts positive allometry specifically in male ornamentation. Nevertheless, male allometric slopes were constrained in aquatic species whereas males of terrestrial species were free to exaggerate the size of their ornaments. Natural selection therefore appears to suppress ornament size in aquatics because of the biomechanical constraints associated with swimming. These differences in within-population static allometry between aquatic and terrestrial species in turn manifested in a greater across-species evolutionary allometric intercept, but not slope, for terrestrial species relative to aquatic and species.</p> <p>5. These findings indicate that the study of ornament allometries can provide useful insights into the role of sexual selection on ornament elaboration and also help reveal the presence of opposing natural selection that might result in alternative allometric patterns. The relationship between static and evolutionary allometries remains complex, and our results caution against the interpretation of evolutionary allometry in the absence of a clear understanding of the underlying static allometries associated with it.</p>

opencc-zeroNov 2021View details →
dryad36/100

The stabilising impact of natural selection on the allometry of sexual ornaments: Fish that escape locomotor constraints exhibit extravagant ornamentation

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publicNov 2021View details →
dryad36/100

Data from: Sexually divergent selection, allometric constraints, and the evolution of sexual dimorphism in cichlids from Lake Tanganyika

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publicAug 2024View details →
dryad36/100

Feather evolution following flight loss in crown group birds: relaxed selection and developmental constraints

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publicFeb 2025View details →
dryad32/100

Data from: Evidence for repeated loss of selective constraint in rhodopsin of amblyopsid cavefishes (Teleostei: Amblyopsidae)

The genetic mechanisms underlying regressive evolution—the degeneration or loss of a derived trait—are largely unknown, particularly for complex structures such as eyes in cave organisms. In several eyeless animals, the visual photoreceptor rhodopsin appeared to retain functional amino-acid sequences. Hypotheses to explain apparent maintenance of function include weak selection for retention of light-sensing abilities and its pleiotropic roles in circadian rhythms and thermotaxis. In contrast, we show that there has been repeated loss of functional constraint of rhodopsin in amblyopsid cavefishes, as at least three cave lineages have independently accumulated unique loss-of-function mutations over the last 10.3 My. While several cave lineages still possess functional rhodopsin, they exhibit increased rates of nonsynonymous mutations that have greater effect on the structure and function of rhodopsin compared to those in surface lineages. These results indicate that functionality of rhodopsin has been repeatedly lost in amblyopsid cavefishes. The presence of a functional copy of rhodopsin in some cave lineages is likely explained by stochastic accumulation of mutations following recent subterranean colonization.

opencc-zeroDec 2011View details →
dryad32/100

Data from: Evolution of resistance to a multiple-herbavore community: genetic correlations, diffuse coevolution, and constraints on the plant's response to selection

Although plants are generally attacked by a community of several species of herbivores, relatively little is known about the strength of natural selection for resistance in multiple-herbivore communities—particularly how the strength of selection differs among herbivores that feed on different plant organs or how strongly genetic correlations in resistance affect the evolutionary responses of the plant. Here, we report on a field study measuring natural selection for resistance in a diverse community of herbivores of Solanum carolinense. Using linear phenotypic-selection analyses, we found that directional selection acted to increase resistance to seven species. Selection was strongest to increase resistance to fruit feeders, followed by flower feeders, then leaf feeders. Selection favored a decrease in resistance to a stem borer. Bootstrapping analyses showed that the plant population contained significant genetic variation for each of 14 measured resistance traits and significant covariances in one-third of the pairwise combinations of resistance traits. These genetic covariances reduced the plant's overall predicted evolutionary response for resistance against the herbivore community by about 60%. Diffuse (co)evolution was widespread in this community, and the diffuse interactions had an overwhelmingly constraining (rather than facilitative) effect on the plant's evolution of resistance.

opencc-zeroDec 2012View details →
dryad32/100

Data from: Selection, constraint and the evolution of coloration in African starlings

Colorful plumage plays a prominent role in evolution of birds, influencing communication (sexual/social selection) and crypsis (natural selection). Comparative studies have focused primarily upon these selective pressures, but the mechanisms underlying color production can also be important by constraining the color gamut upon which selection acts. Iridescence is particularly interesting to study the interaction between selection and color-producing mechanisms because a broad range of colors can be produced with a shared template, and innovations to this template further expand this by increasing the parameters interacting to produce colors. We examine the patterns of ornamentation and dichromatism evolution in African starlings, a group remarkably diverse in color production mechanisms, social systems, and ecologies. We find that the presence of iridescence is ancestral to the group, being predominantly lost in females and cooperative breeders, as well as species with less labile templates. Color-producing mechanisms interact and are the main predictors of plumage ornamentation and elaboration, with little influence of selective pressures in their evolution. Dichromatism, however is influenced by social system and the loss of iridescence. Our results show the importance of considering both selection and constraints, and the different roles that they may have, in the evolution of ornamentation and dimorphism.

opencc-zeroDec 2015View details →
dryad32/100

Data from: Sexual selection, feather wear, and time constraints on the pre-basic molt explain the acquisition of the pre-alternate molt in European passerines

<p><span>Avian feathers need to be replaced periodically to fulfill their functions, with natural, social, and sexual selection presumably driving the evolution of molting strategies. In temperate birds, a common pattern is to molt feathers immediately after the breeding season, the pre-basic molt. However, some species undergo another molt in winter-spring, the pre-alternate molt. Using a sample of 188 European passerine species, Bayesian phylogenetic mixed models, and correlated evolution analyses, we tested whether the occurrence of the pre-alternate molt was positively associated with proxies for sexual selection (sexual selection hypothesis) and non-sexual social selection (social selection hypothesis) and with factors related to feather wear (feather wear hypothesis) and time constraints on the pre-basic molt (time constraints hypothesis). We found that the pre-alternate molt was more frequent in migratory and less gregarious species inhabiting open/xeric habitats and feeding on the wing, and marginally more frequent in species with strong sexual selection and those showing a winter territorial behavior. Moreover, an increase in migratory behavior and sexual selection intensity preceded the acquisition of the pre-alternate molt. These results provide support for the feather wear hypothesis, partial support for the sexual selection and time constraints hypotheses, and no support for the social selection hypothesis.</span></p>

opencc-zeroAug 2022View details →
dryad32/100

Strong sexual selection despite spatial constraints on extra-pair paternity

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publicJan 2020View details →
dryad32/100

Data from: Age-specific breeding success in a wild mammalian population: selection, constraint, restraint, and senescence

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publicApr 2011View details →
dryad32/100

Data from: Evidence for repeated loss of selective constraint in rhodopsin of amblyopsid cavefishes (Teleostei: Amblyopsidae)

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publicOct 2012View details →
dryad32/100

Data from: Evolution of resistance to a multiple-herbavore community: genetic correlations, diffuse coevolution, and constraints on the plant's response to selection

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publicJan 2013View details →
dryad32/100

Data from: Selection, constraint and the evolution of coloration in African starlings

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publicApr 2016View details →
dryad32/100

Data from: Sexual selection, feather wear, and time constraints on the pre-basic molt explain the acquisition of the pre-alternate molt in European passerines

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publicAug 2022View details →
dryad32/100

Data from: Complex constraints on allometry revealed by artificial selection on the wing of Drosophila melanogaster

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publicJun 2016View details →
dryad28/100

Data from: Morph-specific artificial selection reveals a constraint on the evolution of polyphenisms

Theory predicts that the evolution of polyphenic variation is facilitated where morphs are genetically uncoupled and free to evolve towards their phenotypic optima. However, the assumption that developmentally plastic morphs can evolve independently has not been tested directly. Using morph-specific artificial selection, we investigated correlated evolution between the sexes and male morphs of the bulb mite Rhizoglyphus echinopus. Large 'fighter' males have a thick and sharply terminating pair of legs used to kill rival males, while small 'scrambler' males have unmodified legs, and search for unguarded females, avoiding fights. We selected on the relative leg width of only the fighter male morph, tracked the evolutionary responses in fighters and the correlated evolutionary responses in scramblers and females that were untouched by direct selection. Fighters diverged in relative leg thickness after six generations; assaying scramblers and females at the ninth generation we observed correlated responses in relative leg width in both. Our results represent strong evidence for the evolution of intraspecific phenotypic diversity despite correlated evolution between morphs and sexes, challenging the idea that male morphs are genetically uncoupled and free to independen- tly respond to selection. We, therefore, question the perceived necessity for genetic independence in traits with extreme phenotypic plasticity.

opencc-zeroDec 2017View details →
dryad28/100

Data from: Using branch-and-bound algorithms to optimize selection of a fixed-size breeding population under a relatedness constraint

Tree breeders often face the challenge of conserving genetic diversity, while at the same time maximizing response to selection. When selecting advanced-generation breeding populations, the best-performing candidates will quite often be closely related and selecting them without consideration of their relatedness will very quickly erode genetic diversity. Optimal selection will not completely avoid kinship, but rather maximize gain while imposing a constraint on average relatedness. Genetic contributions are most easily optimized if breeders can manage a real, continuous distribution of contributions from parents. While generally possible when establishing seed orchards, unequal contributions to a breeding population may present difficult and time-consuming operational constraints. In these situations, a specified number of parents contributing equally may be a preferred configuration for the breeding population. Here we formulate the selection of a fixed-size breeding population while imposing a constraint on relatedness of the population members. The problem is expressed as a Mixed Integer Quadratically Constrained Optimization (MIQCO) and solved using branch-and-bound techniques (BB). An open-source solver, dsOpt, was developed and embedded into a user-friendly tool, OPSEL, designed to simplify the process of optimizing selection of breeding populations. Case studies optimizing selection of breeding populations for Scots pine and loblolly pine illustrate the superiority of the BB solution compared with selection from ranked lists with restrictions on numbers of genotypes contributed by each full-sib family, and with solutions from GENCONT, a publically available optimum selection program using an algorithm with Lagrangian multipliers. The case studies also illustrate the extreme differences that can occur with respect to time required to confirm the optimality of solutions found by BB.

opencc-zeroDec 2014View details →
dryad28/100

Data from: Predicting the response to simultaneous selection: genetic architecture and physiological constraints

A great deal is known about the evolutionary significance of body size and development time. They are determined by the non-linear interaction of three physiological traits: two hormonal events and growth rate. In this study we investigate how the genetic architecture of the underlying three physiological traits affects the simultaneous response to selection on the two life history traits in the hawk moth Manduca sexta. The genetic architecture suggests that when the two life history traits are both selected in the same direction (to increase or decrease) the response to selection is primarily determined by the hormonal mechanism. When the life history traits are selected in opposite directions (one to increase and one to decrease) the response to selection is primarily determined by factors that affect the growth rate. To determine how the physiological traits affect the response to selection of the life history traits, we simulated the predicted response to ten generations of selection. 83% of our predictions were supported by the simulation. The main components of this physiological framework also exist in unicellular organisms, vertebrates and plants and can thus provide a robust framework for understanding how underlying physiology can determine the simultaneous evolution of life history traits.

opencc-zeroDec 2011View 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