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.
3,183
datasets available to search
ShareScore release 0.9.0
Dataset results
3,183 results for “parenting”
Figure 3 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 3. Egg masses: (A) Pleioplana atomata, (B) Imogine zebra. Scale bars, 500 mm. Pleioplana atomata: (C) two eggs per egg capsule, scale bar 150 mm, (D) conjoined hatchlings, scale bar 100 mm.
Figure 1 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 1. Pleioplana atomata reproductive behaviour: (A) initial encounters, (B) and (C) reciprocal prodding of ventral surface, and (D) copulation. Images are video stills.
Figure 8 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 8. Variation in mean hatching rate (¡1 SE) per batch of eggs with and without parental care in Pleioplana atomata and Imogine zebra. (A, C) Treatment 1 – egg hatching rate for all batches per individual; black bars – with parental care, white bars – without parental care, (B, D) Treatment 2 – three egg batches with parental care and three batches without parental care per individual.
Figure 2 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 2. Imogine zebra reproductive behaviour: (A) initial encounter and gliding over each other, (B) prodding of dorsal surface, (C) unilateral sperm transfer, (D) sperm transfer among multiple animals, (E) spermatophores on dorsal surface. Images are video stills.
Figure 6 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 6. Hatchlings (A) Pleioplana atomata and (B) Imogine zebra, arrowheads indicate caudal cilia. Scale bars, 100 mm.
FIGURE 8 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 8. Dugastella valentina (Ferrer Galdiano, 1924), first juvenile: A, first maxilliped; B, second maxilliped; C, third maxilliped; D, first pereiopod; E magnification of chela; F, third pereiopod; G, third pleopod; H, uropod; I, telson. Scale bars = 0.1 mm.
FIGURE 7 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 7. Dugastella valentina (Ferrer Galdiano, 1924), first juvenile: A, lateral view; B, dorsal view; C, antenna; D, antennule; E, mandible; F, maxillule; G, maxilla. Scale bars= 1 mm (A,B), 0.1 mm (C–G).
FIGURE 6 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 6. Dugastella valentina (Ferrer Galdiano, 1924), telson: A, zoea I; B, zoea II; C, decapodid; third pleopod: D, zoea I; E, zoea II; F, decapodid. Scale bar = 0.5 mm (A–C), 0.25 mm (D–F).
FIGURE 5 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 5. Dugastella valentina (Ferrer Galdiano, 1924), pereiopods first to fifth: A–E, zoea I; F–J, zoea II; K–O, decapodid. Scale bar = 0.25 mm.
FIGURE 3 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 3. Dugastella valentina (Ferrer Galdiano, 1924), mandible: A, zoea I; B, zoea II; C, decapodid; maxillule: D, zoea I; E, zoea II; F, decapodid; maxilla: G, zoea I; H, zoea II; I, decapodid. Scale bars = 0.1 mm.
FIGURE 4 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 4. Dugastella valentina (Ferrer Galdiano, 1924), first maxilliped: A, zoea I; B, zoea II; C, decapodid; second maxilliped: D, zoea I; E, zoea II; F, decapodid; third maxilliped: G, zoea I; H, zoea II; I, decapodid. Scale bar = 0.25 mm.
FIGURE 2 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 2. Dugastella valentina (Ferrer Galdiano, 1924), antennule: A, zoea I; B, zoea II; C, decapodid; antenna: D, zoea I; E, zoea II; F, decapodid. Scale bar = 0.25 mm.
FIGURE 1 in Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care
FIGURE 1. Dugastella valentina (Ferrer Galdiano, 1924), lateral view: A, zoea I; B, zoea II; C, decapodid; dorsal view: D, zoea I; E, zoea II; F, decapodid. Scale bar = 1 mm.
Resequenced tomato MAGIC population parents
<p>The file Sl_MAGIC_population_parents_resequencing.vcf.gz provides the variants of eight highly diverse wild and weedy S. pimpinellifolium (BGV006454, BGV015382, BGV013720 and BGV007145 ) and S. lycopersicum var. cerasiforme (BGV006769, BGV007931, LA2251 and PI487625 ) accessions, which are the parents of a MAGIC population that is currently under development.<br> All the detailed information can be found in the following publication:<br> Gramazio, Pietro, et al. "Morphoagronomic characterization and whole-genome resequencing of eight highly diverse wild and weedy S. pimpinellifolium and S. lycopersicum var. cerasiforme accessions used for the first interspecific tomato MAGIC population." Horticulture Research 7.1 (2020): 1-16.</p>
Nickel and chromium stable isotopic composition of ureilites: implications for the Earth's core formation and differentiation of the ureilite parent body
<p>We report the first Ni and Cr stable isotope data for ureilite meteorites that are the mantle residue of a carbon-rich differentiated planet. Ureilites have similar Ni stable isotope compositions as chondrites, suggesting the core-mantle differentiation of ureilite parent body did not fractionate Ni isotopes. Since the size of Earth is potentially larger than that of ureilite parent body (UPB; with diameter > 690 km), resulting in higher temperatures at the core-mantle boundary of Earth, it can be predicted that the terrestrial core formation may not directly cause Ni stable isotope fractionation. On the other hand, we also report high-precision Cr stable isotope composition of ureilites, including one ureilitic trachyandesite (ALM-A) that is enriched in lighter Cr stable isotopes relative to the main-group ureilites, which suggests the partial melting occurred on UPB. The globally heavy Cr in the UPB compared to chondrites can be caused by sulfur-rich core formation processes.</p>
FIGURE 1 in Sorting out the muddle: taxonomy and nomenclature of Thymus ×porcii (Lamiaceae) and related nothotaxa, with comments on parent species delimitation
FIGURE 1. Distribution map of Thymus pulegioides, Thymus pannonicus and Thymus ×porcii. A. General range of Thymus pulegioides. B. European part of range of Thymus pannonicus. C. Thymus pulegioides and Thymus pannonicus hybridization zone with the occurence of Thymus ×porcii. D, E. Current known localities of Thymus pulegioides var. vestitus within the hybridization zone, with the existing (D) and predicted (E) occurrences of Thymus ×porcii nothovar. opizii [Thymus pannonicus × Thymus pulegioides var. vestitus].
FIGURE 4 in Sorting out the muddle: taxonomy and nomenclature of Thymus ×porcii (Lamiaceae) and related nothotaxa, with comments on parent species delimitation
FIGURE 4. Thymus ×porcii nothovar. calvariensis from locus classicus (Lysa hill in Lviv city, Ukraine). A. General habit. B. Inflorescence. C. Habitat.
FIGURE 6 in Sorting out the muddle: taxonomy and nomenclature of Thymus ×porcii (Lamiaceae) and related nothotaxa, with comments on parent species delimitation
FIGURE 6. Lectotype of Thymus ×opizii, the basionym of Thymus ×porcii nothovar. opizii (PR751622-A and PR751623-B).
Figure 2 in Behavioural parental care repertoire in Frostius pernambucensis (Anura, Bufonidae)
Figure 2. Similarity of yellowish F. pernambucensis colors evidenced both in adults and in newly hatched eggs and tadpoles. (a)–Frostius pernambucensis eggs, eggs and newly hatched tadpoles; (b) – Yellowish iris in a F.pernambucensis individual guarding the spawn (Behavior 19, Table 1); (c). pernambucensis tadpoles being protected by the male; (d) – Partially yellowed front and rear limbs; (e) – Yellowish belly, becoming more intense in the pelvic area near the cloaca (Behavior 10, Table 1); (Photographed by Emerson G. Dias).
Parenting costs time: Changes in pair bond maintenance across pregnancy and infant rearing in a monogamous primate (Plecturocebus cupreus)
<p>Dataset for manuscript submitted to New Directions for Child and Adolescent Development. Abstract for article:</p> <p>Relationships support social animals’ health, but maintaining relationships is challenging. When transitioning to parenthood, new parents balance pair-bond maintenance with infant care. We studied pair-bond maintenance via affiliation in 22 adult titi monkey pairs (<em>Plecturocebus cupreus</em>) for 16 months centered around their first offspring’s birth. Pair affiliation peaked during pregnancy, decreased across the postpartum period, and rose after reaching minimum affiliation 32.6 weeks postpartum. Pairs in which fathers carry infants more than average had lower affiliation at the infant’s birth and return to an increase in affiliation sooner. Parents of infants who were slow to independence had higher rates of affiliation. Titi monkey infants actively prefer their fathers; mothers may avoid their infant-carrying mate, suggesting infants play an active role in parental affiliative decline. Our data supports previous findings that affiliation between partners declines following an infant’s birth, but demonstrates new knowledge about the extent and duration of affiliative decline.</p>
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.