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.
2,608
datasets available to search
ShareScore release 0.9.0
Dataset results
2,608 results for “breed”
Figure 10 in Morphology of the puparium and breeding sites of eight species of Heleomyzidae (Diptera)
Figure 10. Heteromyzinae, head skeletons, left hand figures, whole structure, lateral view, mandible to the right, right hand figures, dorsal view of intermediate sclerite and mandible in that order, scale bar 0.25 mm, (A, B) Tephrochlamys flavipes, (C, D) Tephrochlamys tarsalis, (E, F) Heteromyza rotundicornis.
Figure 9 in Morphology of the puparium and breeding sites of eight species of Heleomyzidae (Diptera)
Figure 9. Heleomyzinae, head skeletons, left hand figures, whole structure, lateral view, mandible to the right, right hand figures, dorsal view of intermediate sclerite and mandible in that order, scale bar 0.25 mm, (A, B) Eccoptomera microps, (C, D) Scoliocentra brachypterna, (E, F) Heleomyza borealis.
Figure 5 in Morphology of the puparium and breeding sites of eight species of Heleomyzidae (Diptera)
Figure 5. Suillinae, posterior spiracles, apical view, scale bar 0.1 mm, (A) Suillia variegata, (B) Suillia ustulata, (C) Suillia laevifrons.
Figure 1 in Morphology of the puparium and breeding sites of eight species of Heleomyzidae (Diptera)
Figure 1. Heleomyzidae, whole puparia, lateral view, anterior end to the left, dorsal margin uppermost, (A) Heteromyza rotundicornis, length 5 mm, (B) Heleomyza borealis, length 6 mm, (C) Suillia variegata, length 4 mm.
Figure 1 in Breeding biology of the golden parrotbill (Paradoxornis verreauxi) (Aves: Timaliidae) in southwestern China
Figure 1. An adult Golden Parrotbill with nest material in its bill (photograph by Suixing Tian, with permission).
Figure 1 in Natural history of Phyllomedusa megacephala (Miranda-Ribeiro, 1926) (Anura: Hylidae) in southeastern Brazil, with descriptions of its breeding biology and male territorial behaviour
Figure 1. Photographs taken during field work to show the colour patterns on the right flanks of Phyllomedusa megacephala for individual recognition. The figure shows pictures of two individuals.
Figure 2 in Natural history of Phyllomedusa megacephala (Miranda-Ribeiro, 1926) (Anura: Hylidae) in southeastern Brazil, with descriptions of its breeding biology and male territorial behaviour
Figure 2. (A) Summary of the events observed as part of the territorial behaviour of Phyllomedusa megacephala males. (B) Summary of the events observed as part of the breeding behaviour of P. megacephala.
Data from: Timing of spring departure of long distance migrants correlates with previous year's conditions at their breeding site
<p>Precise timing of the migration is crucial for animals targeting seasonal resources at locations encountered across their annual cycle. Upon departure, long distance migrants need to anticipate unknown environmental conditions at their arrival site, and they do zkzdsxso with their internal annual clock. Here, we tested the hypothesis that long distance migrants synchronize their circannual clock according to the phenology of their environment during the breeding season, and therefore adjust their spring departure date according to the conditions encountered at their breeding site the year before. To this end, we used tracking data of Eurasian curlews from different locations and combined movement data with satellite-extracted green-up dates at their breeding site. Spring departure date was better explained by green-up date of the previous year, while arrival date at the breeding site was better explained by latitude and longitude of the breeding site, suggesting that other factors impacted migration timing <i>en route</i>. On a broader temporal scale, our results suggest that long distance migrants may be able to adjust their migration timing to advancing spring dates in the context of climate change. </p>
Figure 1 in Breeding behaviour of the Omei tree frog Rhacophorus omeimontis (Anura: Rachophoridae) in a subtropical montane region
Figure 1. Pictures of breeding Rhacophorus omeimontis. (a) Group spawning in tree leaves at Pond A; (b) leaf nest at Pond A; (c) group spawning at Pond B; and (d) spawning site at Pond B.
Figure 4 in Breeding behaviour of the Omei tree frog Rhacophorus omeimontis (Anura: Rachophoridae) in a subtropical montane region
Figure 4. Relationship between number of joining males and percentage clutch fertilization of Rhacophorus omeimontis at Pond A.
Figure 3 in Breeding behaviour of the Omei tree frog Rhacophorus omeimontis (Anura: Rachophoridae) in a subtropical montane region
Figure 3. Relationship between mean egg size and clutch size of Rhacophorus omeimontis in Pond A (broken line) and Pond B (solid line).
Figure 2 in Breeding behaviour of the Omei tree frog Rhacophorus omeimontis (Anura: Rachophoridae) in a subtropical montane region
Figure 2. Analysis of Rhacophorus omeimontis vegetation-use at Pond B. Relative occurrence at the pond perimeter of different vegetation types (black bars) and percentage of plant species used by R. omeimontis to construct foam nests (white bars). Plant species used for the construction of foam nests were: (a) Rhizoma dryoteris; (b) Parathelypteris glanduligera; (c) Artemisia princes; (d) Urtica cannabina; and (e) Plantago asiatica.
Figure 3 in Breeding biology of the rapids frog Limnomedusa macroglossa (Anura: Cycloramphidae) in southern Brazil
Figure 3. Relation of encounter rate (number of individuals recorded by month/monthly sampling effort) of Limnomedusa macroglossa with temperature (A) and photoperiod (B) in Rio Grande do Sul state, southern Brazil (n518 months).
Figure 2. Bars represent average temperature from 1961 in Breeding biology of the rapids frog Limnomedusa macroglossa (Anura: Cycloramphidae) in southern Brazil
Figure 2. Bars represent average temperature from 1961 to 1990 in the neighbouring municipality of Santa Maria, a pattern similar to that of Itaara. Temperature data were obtained from the website of the Instituto Nacional de Meteorologia, Brazil (www. inmet.gov.br). Timelines below show the occurrence of vocalization, amplexes/egg deposition, tadpoles and juveniles of Limnomedusa macroglossa from Rio Grande do Sul state, southern Brazil.
Figure 1 in Breeding biology of the rapids frog Limnomedusa macroglossa (Anura: Cycloramphidae) in southern Brazil
Figure 1. Partial view of the study site S1 (A); amplexed pair (B) and egg clutch (C) of Limnomedusa macroglossa in Rio Grande do Sul state, southern Brazil.
Figure 2 in Population size, breeding rates and conservation status of Eurasian black vulture in the Dadia National Park, Thrace, NE Greece
Figure 2. The trend of breeding success (Nfled/Ninc ×100) of the black vulture population for the period 1994–2005.
Figure 1 in Population size, breeding rates and conservation status of Eurasian black vulture in the Dadia National Park, Thrace, NE Greece
Figure 1. Maximum (Nmax) annual number of individuals and breeding pairs (Ninc) of the black vulture population in the Dadia NP for the period 1987–2005.
FIGURE 6 in Taxonomic consideration of eight Chinese bisexual Artemia populations, based on the morphology of frontal knob and gonopod and the result of cross-breeding tests
FIGURE 6. Distal gonopod spines of different Artemia populations. (A, B) Gonopods of URM to show the position of spines on distal gonopod (in A, the thickness of finger-like tip is inflated because the specimen is molting and the old skeleton has not been stripped from the finger-like tip). (C, D) Exolateral spines of URM. (E) Posterior spines of URM. (F) Gonopod of SAL to show the position of spines on distal gonopod. (G) Posterior spines of SAL. (H) Exolateral spines of SAL. (I) An exolateral spine of SAL with bifurcated tip. (J) Gonopod of SFB to show the position of spines on distal gonopod. (K, L) Exolateral spines of SFB. (M) A spine located on the anterior surface of distal gonopod of SFB. (N) Gonopod of PER to show the position of spines on distal gonopod. BG = basal gonopod; BGS = basal gonopod spine; DG = distal gonopod; ES = exolateral spines; FT = finger-like tip; PS = posterior spines. Abbreviations of Artemia populations see Table 1. Scale bars: A, B, F, J and N = 50 µm; C, E, G, H and I = 10 µm; D, K, L and M = 5 µm.
FIGURE 3 in Taxonomic consideration of eight Chinese bisexual Artemia populations, based on the morphology of frontal knob and gonopod and the result of cross-breeding tests
FIGURE 3. SEM photographs of the frontal knobs of Chinese bisexual Artemia populations to show the appearance of frontal knobs (A, C, E and G; frontal view) and the arrangement of spines (B, D, F and H). (A, B) LGC. (C, D) CMC. (E, F) DDC. (G, H) JBCK. Abbreviations of Artemia populations see Table 1. Scale bars: A, C, E and G = 100 µm; B, D, F and H = 20 µm.
FIGURE 4 in Taxonomic consideration of eight Chinese bisexual Artemia populations, based on the morphology of frontal knob and gonopod and the result of cross-breeding tests
FIGURE 4. The appearance of the distal gonopod of five bisexual Artemia populations. (A) SIN. (B) LGC. (C) URM. (D) SAL. (E) SFB. (F) PER. BG = basal gonopod; DG = distal gonopod; FT = finger-like tip. Basal gonopod spine is arrowed. Abbreviations of Artemia populations see Table 1. Scale bars = 100 µm.
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.