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20 results for “Reproductive and productive”

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zenodo40/100

Рис. 9. Связь межΔу чисΛенностью и проΔуктивностью самок Heterodera glycines Fig. 9. Relationship between the number and productivity of Heterodera glycines females in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions

Рис. 9. Связь межΔу чисΛенностью и проΔуктивностью самок Heterodera glycines Fig. 9. Relationship between the number and productivity of Heterodera glycines females

opencc-by-4.0Feb 2021View details →
zenodo40/100

Fig. 7 in Reproductive behavior and sex pheromone production in Eutectona machaeralis (Lepidoptera: Crambidae)

Fig. 7. Mean behavioral responses of Eutectona machaeralis males to sex pheromone gland crude extracts and the control in a wind tunnel. Means with the same letter are not significantly different (P> 0.05).

opencc-by-4.0Jun 2018View details →
zenodo40/100

Fig. 2 in Reproductive behavior and sex pheromone production in Eutectona machaeralis (Lepidoptera: Crambidae)

Fig. 2. The influence of age on daily emergence of Eutectona machaeralis adults (mixed sex) in the laboratory during scotophase. Values with the same letter are not significantly different (P> 0.05).

opencc-by-4.0Jun 2018View details →
zenodo40/100

Fig. 5 in Reproductive behavior and sex pheromone production in Eutectona machaeralis (Lepidoptera: Crambidae)

Fig. 5. Mean electroanntenogram response of male Eutectona machaeralis to sex pheromone gland crude extract obtained from 2-d-old virgin females at different hours during scotophase. Means with the same letter are not significantly different (P> 0.05).

opencc-by-4.0Jun 2018View details →
zenodo40/100

Fig. 4 in Reproductive behavior and sex pheromone production in Eutectona machaeralis (Lepidoptera: Crambidae)

Fig. 4. Mean percentage of Eutectona machaeralis females that exhibited calling behavior during scotophase. Means with the same letter are not significantly different (P> 0.05).

opencc-by-4.0Jun 2018View details →
zenodo36/100

Fig. 1 in Reproductive behavior and sex pheromone production in Eutectona machaeralis (Lepidoptera: Crambidae)

Fig. 1. Hourly emergence of Eutectona machaeralis adults in the laboratory during scotophase.

opencc-by-4.0Jun 2018View details →
dryad36/100

Towards rainy high Arctic winters: how experimental icing and summer warming affect tundra plant phenology, productivity and reproduction

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publicDec 2025View details →
dryad36/100

A potential role for epigenetic mechanisms enabling appropriate seasonal reproductive transitions of liver yolk-precursor production

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publicOct 2025View details →
dryad36/100

Total, foliar, and reproductive fine litter production for up to 38 years for four old-growth forests in central Panama

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publicDec 2024View details →
dryad32/100

Data from: Berry production drives bottom-up effects on body mass and reproductive success in an omnivore

Obligate herbivores dominate studies of the effects of climate change on mammals, however there is limited empirical evidence for how changes in the abundance or quality of plant food affect mammalian omnivores. Omnivores can exploit a range of different food resources over the course of a year, but they often rely on seasonally restricted highly nutritious fruiting bodies during critical life stages. Brown bears Ursus arctos in Sweden are dependent on berries for fattening before entering hibernation. We used a ten-year time series to evaluate the effect of temperature and snow on annual variation in berry abundance and how this variation affected bears. We found marked interannual variation in berry production of bilberry Vaccinium myrtillus and lingonberry V. vitis-idaea, that we could attribute in part to temperature during plant dormancy and flowering and precipitation during fruit ripening. Both, autumn weights of female bears and spring weights of yearling bears increased linearly with bilberry abundance. When bilberry abundance was low, lightweight female bears had a lower reproductive success than females in better condition. This effect vanished when food abundance was above average, indicating that lightweight females could compensate for their initial weight during good bilberry years. Our study highlights the importance of considering individuals' dynamic responses to variation in food availability, which leave some more vulnerable to food shortage than others. Individual life-history heterogeneity in response to resource variation likely affects long-term population recruitment. Our findings emphasize that Scandinavian bears can be dependent on a single food resource during a critical period of the year and are therefore less resilient to environmental change than expected for an omnivore. Future climate scenarios predict ambiguous trends for weather covariates that affected crucial stages of berry phenology, preventing a clear prognosis of how climate change may affect long-term bilberry production.

opencc-zeroDec 2016View details →
dryad32/100

Data from: Variation in patriline reproductive success during queen production in orphaned colonies of the thelytokous ant Cataglyphis cursor

In genetically diverse insect societies (polygynous or polyandrous queens), the production of new queens can set the ground for competition among lineages. This competition can be very intense when workers can reproduce using thelytoky as worker patrilines that manage to produce new queens gain a huge benefit. Selection at the individual level might then lead to the evolution of cheating genotypes, i.e. genotypes that reproduce more than their fair share. We studied the variation in reproductive success among worker patrilines in the thelytokous and highly polyandrous ant Cataglyphis cursor. Workers produce new queens by thelytoky in orphaned colonies. The reproductive success of each patriline was assessed in 13 orphaned colonies using genetic analysis of 433 workers and 326 worker-produced queens. Our results show that patrilines contributed unequally to queen production in half of the colonies and the success of patrilines was function of their frequencies in workers. However, over all colonies we observed a significant difference in the distribution of patrilines between workers and worker-produced queens, and this difference was significant in three out of 13 colonies. In addition, six colonies contained a low percentage of foreign workers (drifters) and in one colony they produced a disproportionably high number of queens. Hence, we found some evidence for the occurrence of rare cheating genotypes. Nevertheless, cheating appears to be less pronounced than in the Cape Honey bee, a species with a similar reproductive system. We argue that worker reproduction by parthenogenesis might not be common in natural populations of C. cursor.

opencc-zeroDec 2010View details →
dryad32/100

Data from: Effects of nitrogen deposition on reproduction in a masting tree: benefits of higher seed production are trumped by negative biotic interactions

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publicSep 2017View details →
dryad32/100

Data from: Berry production drives bottom-up effects on body mass and reproductive success in an omnivore

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publicMay 2017View details →
dryad32/100

Data from: Variation in patriline reproductive success during queen production in orphaned colonies of the thelytokous ant Cataglyphis cursor

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publicFeb 2011View details →
dryad28/100

Data from: Nutrition during sexual maturation affects competitive ability but not reproductive productivity in burying beetles

1. Food availability can be unpredictable. When food becomes more abundant following a period of low food availability, developing larvae or juveniles often allocate resources preferentially towards increasing growth. This has important long-term effects on adult phenotypes and longevity. Despite the importance of strategic resource allocation during early development, few studies have examined how changes in resource availability during other windows of development affect reproductive strategies and fitness independent of growth. 2. We manipulated food availability in a burying beetle, Nicrophorus vespilloides, during a subadult period of sexual maturation when individuals cannot increase structural size but are still undergoing reproductive maturation. 3. In contrast to the trade-offs during larval or juvenile growth, beetles that experienced delayed feeding during reproductive maturation allocated resources preferentially towards maintaining both reproductive function and longevity. 4. In both sexes, delayed feeding beetles were much less successful in competition for carcasses. However, delayed feeding males and females provided similar amounts of parental care and did not differ in reproductive success or longevity. 5. These results indicate that the nutritional environment experienced during a key developmental window may be an important determinant of the expression of alternative reproductive strategies in adulthood, independent of body size.

opencc-zeroDec 2012View details →
dryad28/100

Data from: Nutrition during sexual maturation affects competitive ability but not reproductive productivity in burying beetles

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publicJul 2013View details →
geo24/100

Metformin alters liver metabolism to sustain egg production in the reproductively aging broiler breeder hen

GEO Series GSE286522. Gallus gallus. 15 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJan 2025View details →
ClinicalTrials.gov24/100

Mitochondrial Energy Production in ART (Assisted Reproductive Technology )

ClinicalTrials.gov study NCT02727400. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Multi-product PrEP Delivery to Young Women Seeking Reproductive Health Services and Coverage of HIV Prevention

ClinicalTrials.gov study NCT07076043. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo16/100

High throughput small RNA and transcriptome sequencing reveal reproduction-related microRNAs and mRNA in ovary of Geese in Counter-Season Production

GEO Series GSE130245. Anser cygnoides. 6 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2019View 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