Skip to main content
Powered by ShareScore

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.

143

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

143 results for “sex roles”

Learn how ShareScore rates datasets ↗
ClinicalTrials.gov32/100

Sympathetic Neurovascular Transduction: Role of Adrenergic Receptors and Sex Differences

ClinicalTrials.gov study NCT05997732. IPD Sharing: Not stated. Countries: 1. Publications: 5.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Sex roles, parental care and offspring growth in two contrasting coucal species

Open the record for dataset details and reuse information.

publicSep 2016View details →
dryad32/100

Data from: Duetting behavior varies with sex, season, and singing role in a tropical oriole (Icterus icterus)

Open the record for dataset details and reuse information.

publicMay 2017View details →
dryad32/100

Data from: Social monogamy versus polyandry: ecological factors associated with sex-roles in two closely related birds within the same habitat

Open the record for dataset details and reuse information.

publicMay 2015View details →
dryad32/100

Data from: Gene flow mediates the role of sex chromosome meiotic drive during complex speciation

Open the record for dataset details and reuse information.

publicDec 2018View details →
dryad32/100

Data from: Sex differences in senescence: the role of intra-sexual competition in early adulthood

Open the record for dataset details and reuse information.

publicJun 2015View details →
dryad32/100

Data from: Sex-specific arrival times on the breeding grounds: hybridizing migratory skuas provide empirical support for the role of sex ratios

Open the record for dataset details and reuse information.

publicOct 2015View details →
dryad32/100

Data from: Differential effects of maternal yolk androgens on male and female offspring: a role for sex-specific selection?

Open the record for dataset details and reuse information.

publicJul 2016View details →
dryad32/100

Data from: Female ornamentation and the fecundity trade-off in a sex-role reversed pipefish

Open the record for dataset details and reuse information.

publicJul 2019View details →
dryad32/100

Data from: The contributions of premating and postmating selection episodes to total selection in sex-role-reversed Gulf pipefish

Open the record for dataset details and reuse information.

publicMay 2013View details →
dryad32/100

Data from: The relationship between female brooding and male nestling provisioning: does climate underlie geographic variation in sex roles?

Open the record for dataset details and reuse information.

publicJun 2016View details →
dryad32/100

Data from: Genetic structure and rabies spread potential in raccoons: the role of landscape barriers and sex-biased dispersal

Open the record for dataset details and reuse information.

publicDec 2011View details →
dryad32/100

Data from: No evidence for size-assortative mating in the wild despite mutual mate choice in sex-role-reversed pipefishes

Open the record for dataset details and reuse information.

publicNov 2014View details →
dryad32/100

Mapping and assembly of the Midas cichlid male-specific region supports molecular parallelism in the evolution of a master sex-determining role for amhr2

Open the record for dataset details and reuse information.

publicOct 2022View details →
dryad32/100

Data from: Sex-specific responses to sexual familiarity, and the role of olfaction in Drosophila

Open the record for dataset details and reuse information.

publicSep 2013View details →
dryad32/100

Data from: The effects of synthetic estrogen exposure on pre-mating and post-mating episodes of selection in sex-role-reversed Gulf pipefish

Open the record for dataset details and reuse information.

publicJul 2013View details →
dryad28/100

Data from: Neuroendocrine correlates of sex-role reversal in barred buttonquails

Sex differences in brain structure and behaviour are well documented among vertebrates. An excellent model exploring the neural mechanisms of sex differences in behaviour is represented by sex-role-reversed species. In the majority of bird species, males compete over access to mates and resources more strongly than do females. It is thought that the responsible brain regions are therefore more developed in males than in females. Because these behaviours and brain regions are activated by androgens, males usually have increased testosterone levels during breeding. Therefore, in species with sex-role reversal, certain areas of the female brain should be more developed or steroid hormone profiles should be sexually reversed. Here, I studied circulating hormone levels and gene expression of steroid hormone receptors and aromatase in a captive population of barred buttonquails (Turnix suscitator). While females performed courtship and agonistic behaviours, there was no evidence for sexually reversed hormone profiles. However, I found female-biased sex differences in gene expression of androgen receptors in several hypothalamic and limbic brain regions that were already in place at hatching. Such sex differences are not known from non-sex-role-reversed species. These data suggest that increased neural sensitivity to androgens could be involved in the mechanisms mediating sex-role-reversed behaviours.

opencc-zeroDec 2015View details →
dryad28/100

Data from: The size advantage model of sex allocation in the protandrous sex-changer Crepidula fornicata: role of the mating system, sperm storage, and male mobility

Sequential hermaphroditism is adaptive when the reproductive value of an individual varies with size or age, and this relationship differs between males and females. In this case, theory shows that the lifetime reproductive output of an individual is increased by changing sex (a hypothesis referred to as the size-advantage model). Sex-linked differences in size-fitness curves can stem from differential costs of reproduction, the mating system, and differences in growth and mortality between sexes. Detailed empirical data is required to disentangle the relative roles of each of these factors within the theory. Quantitative data are also needed to explore the role of sperm storage, which has not yet been considered with sequential hermaphrodites. Using experimental rearing and paternity assignment, we report relationships between size and reproductive success of Crepidula fornicata, a protandrous (male-first) gastropod. Male reproductive success increased with size due to the polygamous system and stacking behavior of the species, but females nonetheless had greater reproductive success than males of the same size, in agreement with the size-advantage theory. Sperm storage appeared to be a critical determinant of success for both sexes, and modeling the effect of sperm storage showed that it could potentially accelerate sex change in protandrous species.

opencc-zeroDec 2014View details →
dryad28/100

Data from: Darwinian sex roles confirmed across the animal kingdom

Since Darwin's conception of sexual selection theory, scientists have struggled to identify the evolutionary forces underlying the pervasive differences between male and female behavior, morphology, and physiology. The Darwin-Bateman paradigm predicts that anisogamy imposes stronger sexual selection on males, which, in turn, drives the evolution of conventional sex roles in terms of female-biased parental care and male-biased sexual dimorphism. Although this paradigm forms the cornerstone of modern sexual selection theory, it still remains untested across the animal tree of life. This lack of evidence has promoted the rise of alternative hypotheses arguing that sex differences are entirely driven by environmental factors or chance. We demonstrate that, across the animal kingdom, sexual selection, as captured by standard Bateman metrics, is indeed stronger in males than in females and that it is evolutionarily tied to sex biases in parental care and sexual dimorphism. Our findings provide the first comprehensive evidence that Darwin's concept of conventional sex roles is accurate and refute recent criticism of sexual selection theory.

opencc-zeroDec 2015View details →
dryad28/100

Data from: Sexual dimorphism in epicuticular compounds despite similar sexual selection in sex role-reversed seed beetles

Sexual selection imposed by mating preferences is often implicated in the evolution of both sexual dimorphism and divergence between species in signalling traits. Epicuticular compounds (ECs) are important signalling traits in insects and show extensive variability among and within taxa. Here, we investigate whether variation in the multivariate EC profiles of two sex role-reversed beetle species, Megabruchidius dorsalis and Megabruchidius tonkineus, predicts mate attractiveness and mating success in males and females. The two species had highly distinct EC profiles and both showed significant sexual dimorphism in ECs. Age and mating status in both species were also distinguishable by EC profile. Males and females of both species showed significant association between their EC profile and attractiveness, measured both as latency to mating and as success in mate-choice trials. Remarkably, the major multivariate vector describing attractiveness was correlated in both species, both sexes, and in both choice and no-choice experiments such that increased attractiveness was in all cases associated with a similar multivariate modification of EC composition. Furthermore, in both sexes this vector of attractiveness was associated with more male-like EC profiles, as well as those characterizing younger and nonvirgin individuals, which might reflect a general preference for individuals of high condition in both sexes. Despite significant sexual selection on EC composition, however, we found no support for the proposition that sexual selection is responsible for divergence in ECs between these species.

opencc-zeroDec 2016View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

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