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59 results for “behavioural development”
Figure 1 in Life-history traits of the Brazilian litter-dwelling scorpion: post-embryonic development and reproductive behaviour in Ananteris mauryi Lourenço, 1982 (Scorpiones: Buthidae)
Figure 1. The courtship and mating sequences in Ananteris mauryi Lourenço (1982). (a) Initiation; (b) promenade à deux; (c) insemination and separation. M, male; F, female.
Effects of Psychosocial Stimulation and Cash on Children's Development and Behaviour
ClinicalTrials.gov study NCT03281980. IPD Sharing: UNDECIDED. Countries: 1. Publications: 14.
A Study of the Impact of Hemophilia and Its Treatment on Brain Development, Thinking and Behaviour in Children With Hemophilia
ClinicalTrials.gov study NCT03660774. IPD Sharing: YES. Countries: 1. Publications: 2.
Development and Validation of an Actimetric Protocol to Quantify Physical Activity and Sedentary Behaviour in Post-stroke Subjects
ClinicalTrials.gov study NCT06943014. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effects of a Multiple Sclerosis Relapse Therapy on Offspring Neurocognitive Development and Behaviour
ClinicalTrials.gov study NCT04832269. IPD Sharing: NO. Countries: 1. Publications: 19.
Data from: The development of individual differences in cooperative behaviour: maternal glucocorticoid hormones alter helping behaviour of offspring in wild meerkats
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Data from: Predictors of alcohol consumption among in-school adolescents in the Central Region of Ghana: a baseline information for developing cognitive-behavioural interventions
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Data from: A strong genetic correlation underlying a behavioural syndrome disappears during development because of genotype-age interactions
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Data from: Successful despite poor flight performance: range expansion is associated with enhanced exploratory behaviour and fast development
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Figure 4 from: Postoy V, Kukhtenko H, Vyshnevska L, Gladukh I, Semchenko K (2019) Study of rheological behaviour of hydroxyethyl cellulose gels in the development of the composition and technology of the medicine with anti-inflammatory activity. Pharmacia 66(4): 187-192. https://doi.org/10.3897/pharmacia.66.e37267
Figure 4 Dependence of the shear stress (τ, Ra) of HEC gels with the PG content from the gradient of shear rate (γ, s-1) and the dependence of the structural (dynamic) viscosity (η, Ра s) on the gradient of the shear rate (τ, Ra).
Figure 3 from: Postoy V, Kukhtenko H, Vyshnevska L, Gladukh I, Semchenko K (2019) Study of rheological behaviour of hydroxyethyl cellulose gels in the development of the composition and technology of the medicine with anti-inflammatory activity. Pharmacia 66(4): 187-192. https://doi.org/10.3897/pharmacia.66.e37267
Figure 3 The dependence of the shear stress (τ, Ra) of HEC gels with PEO-400 content on the gradient of shear rate (γ, s-1) and the dependence of the structural (dynamic) viscosity (η, Ra s) on the gradient of the shear rate (τ, Ra).
Figure 5 from: Postoy V, Kukhtenko H, Vyshnevska L, Gladukh I, Semchenko K (2019) Study of rheological behaviour of hydroxyethyl cellulose gels in the development of the composition and technology of the medicine with anti-inflammatory activity. Pharmacia 66(4): 187-192. https://doi.org/10.3897/pharmacia.66.e37267
Figure 5 The dependence of the shear stress (τ, Ra) of the combined gel with test composition, Troxerutin and Thiotriazolinum on the gradient of shear rate (γ, s-1) and the dependence of the structural (dynamic) viscosity (η, Ra s) on the gradient of the shear rate (τ , Ra).
Figure 2 from: Postoy V, Kukhtenko H, Vyshnevska L, Gladukh I, Semchenko K (2019) Study of rheological behaviour of hydroxyethyl cellulose gels in the development of the composition and technology of the medicine with anti-inflammatory activity. Pharmacia 66(4): 187-192. https://doi.org/10.3897/pharmacia.66.e37267
Figure 2 The dependence of the shear stress (τ, Ra) of HEC gels with the content of PEG-40 hydrogenated castor oil on the gradient of shear rate (γ, s-1) and the dependence of the structural (dynamic) viscosity (η, Ra s) on the gradient of the shear rate (τ, Ra).
Figure 1 from: Postoy V, Kukhtenko H, Vyshnevska L, Gladukh I, Semchenko K (2019) Study of rheological behaviour of hydroxyethyl cellulose gels in the development of the composition and technology of the medicine with anti-inflammatory activity. Pharmacia 66(4): 187-192. https://doi.org/10.3897/pharmacia.66.e37267
Figure 1 The dependence of the shear stress (τ, Ra) of the HEC gelson the gradient of the shear rate (γ, s-1) and the dependence of the structural (dynamic) viscosity (η, Ра s) on the gradient of the shear rate (τ, Ra).
Figure 8 in Larval development and emigration behaviour during sea-to-land transition of the land hermit crab Coenobita brevimanus Dana, 1852 (Crustacea: Decapoda: Anomura: Coenobitidae) under laboratory conditions
Figure 8. Coenobita brevimanus, megalopa: (A–E) first to fifth pereiopods, respectively. Scale bar: 100 μm.
Figure 9 in Larval development and emigration behaviour during sea-to-land transition of the land hermit crab Coenobita brevimanus Dana, 1852 (Crustacea: Decapoda: Anomura: Coenobitidae) under laboratory conditions
Figure 9. The proportion of all surviving megalopae and juveniles of Coenobita brevimanus that were on land (○), the proportion carrying shells (Δ), the proportion without shells on land (×) and the proportion of animals found on land that were buried in the sand (●) (A, C), and numbers of megalopae (MG) and juveniles (C1 and C2, first and second crab stages) (B, D) in the two culture groups. (A, B) Megalopae could access land within 24 h after metamorphosing (group 1). (C, D) Megalopae could access land when they walked steadily while wearing shells (group 2). (D) The cumulative number of megalopae that transferred to land (dashed line) is also included for culture group 2.
Figure 6 in Larval development and emigration behaviour during sea-to-land transition of the land hermit crab Coenobita brevimanus Dana, 1852 (Crustacea: Decapoda: Anomura: Coenobitidae) under laboratory conditions
Figure 6. Coenobita brevimanus, fourth zoea: (A) antennule; (B) antenna; (C) mandibles; (D) maxillule; (E) maxilla; (F) first maxilliped; (G) second maxilliped; (H) third maxilliped; (I) telson; (J) pleopod. Scale bars: 100 μm (A–C, E–J) or 50 μm (D).
Plastic adjustments of biparental care behaviour across embryonic development under elevated temperature in a marine ectotherm
<p>Phenotypic plasticity in parental care investment allows organisms to promptly respond to rapid environmental changes by potentially benefiting offspring survival and thus parental fitness. To date, a knowledge gap exists on whether plasticity in parental care behaviours can mediate responses to climate change in marine ectotherms. Here, we assessed the plasticity of parental care investment under elevated temperatures in a gonochoric marine annelid with bi-parental care, Ophryotrocha labronica, and investigated its role in maintaining the reproductive success of this species in a warming ocean. We measured the time individuals spent carrying out parental care activities across three phases of embryonic development, as well as the hatching success of the offspring as a proxy for reproductive success, at control (24°C) and elevated (27°C) temperature conditions. Under elevated temperature we observed: (i) a significant decrease in total parental care activity, underpinned by a decreased in male and simultaneous parental care activity, in the late stage of embryonic development; and ii) a reduction of hatching success, that was however not significantly related to changes in parental-care activity levels. These findings, along with the observed unaltered somatic growth of parents and decreased brood size, suggest that potential cost-benefit trade-offs between offspring survival (i.e. immediate fitness) and parents somatic condition (i.e. longer-term fitness potential) may occur under ongoing ocean warming. Finally, our results suggest that plasticity in parental care behaviour is a mechanism able to partially mitigate the negative effects of temperature-dependent impacts.</p>
Dataset for Using deep learning interpretability to study the development of drawing behaviour in children
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Figure 4 in Reproductive behaviour and development dynamics of Odontophrynus cordobae (Anura, Cycloramphidae)
Figure 4. Dynamics of larval development for a complete cohort of Odontophrynus cordobae.
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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.
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.