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Fig. 1 in A new species of Oopeltidae (Mollusca, Pulmonata, Arionoidea), with a revision of the subfamily Ariopeltinae and remarks on its affinities within the family and superfamily
Fig. 1. Ariostralis nebulosa, genital system. Abbreviations: ALB GL – albumen gland, G A – genital aperture, G ATR – genital atrium, OV – free oviduct, OVOT – ovotestis, PR – penis retractor muscle, SPOV – spermoviduct, SPT – spermatheca, Vag – vagina, VAG B – vaginal bulb, Vd – vas deferens, 1–4 indicate the successive parts of the penis. (From Sirgel 1985)
Figs 3, 4 in A new species of Oopeltidae (Mollusca, Pulmonata, Arionoidea), with a revision of the subfamily Ariopeltinae and remarks on its affinities within the family and superfamily
Figs 3, 4. Ariopelta capensis, genital system: (3) details of the genital system (from Sirgel 1985); (4) distal part of genital system with vaginal bulb cut open to show its interior. Abbreviations: ALB GL – albumen gland, G A – genital aperture, G ATR – genital atrium, LAM – calcareous ring-shaped lamellae intruding into lumen of vaginal bulb, O SPD – opening of spermathecal duct, OV – free oviduct, OVOT – ovotestis, PR – penis retractor muscle, SPD – spermathecal duct, SPOV – spermoviduct, SPT – spermatheca, VAG – vagina, VAG B – vaginal bulb, Vd – vas deferens, 1–4 indicate the successive parts of the penis.
Figure 9 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 9. Dissected male reproductive accessory sex glands from (a) Paramelomys rubex, (b) Uromys caudimaculatus, and (c) Hyomys goliath. Note large sacculated seminal vesicles in (a) and (b) with coagulating glands on their inner curvatures; H. goliath has rather different gross morphology of seminal vesicles and coagulating glands and strikingly large preputial glands (PG). SV = seminal vesicles, CG = coagulating glands, P = prostate glands, AG = ampullary glands, BU = bulbourethral glands, PG = preputial glands, and DD = ductus deferens. Scale bars a–c = 10 mm.
Figure 8 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 8. Scanning electron micrographs of spermatozoa from (a) Lorentzimys nouhuysi, (b) Mammelomys lanosus, (c) Mammelomys rattoides, (d) Coccymys shawmayeri, (e) Xenuromys barbatus, and (f) Rattus niobe. Scale bars a = 1.5 µm, b–f = 2.5 µm.
Figure 6 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 6. Scanning electron micrographs of spermatozoa from (a) Pseudohydromys pumehanae,(b) Melomys lutillus,(c) Paramelomys platyops, (d) Uromys anak, (e) Uromys caudimaculatus, and (f) Chiruromys lamia. AH = apical hook and VPs = ventral processes of sperm head. Scale bars a = 2 µm, b = 1.3 µm, c = 2 µm, d = 1 µm, e and f = 2 µm.
Figure 3 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 3. Boxplot of relative testes mass (g) for species in the divisions (H) Hydromys, (U) Uromys, (P) Pogonomys, (M) Mallomys, and (R) Rattus.
Figure 7 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 7. Scanning electron micrographs of spermatozoa from (a) Chiruromys vates, (b) Pogonomys loriae with inset a fluorescent LM stained with DAPI showing nucleus, (c) Pogonomys macrourus, (d) Pogonomys sylvestris, (e) Hyomys goliath with arrow indicating ventral spike on sperm head, and (f) Mallomys aroaensis inset fluorescent LM stained with DAPI showing nucleus. AH = apical hook and VPs = ventral processes of sperm head. Scale bars a–d = 0.7 µm, e and f = 1.4 µm.
Figure 4 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 4. Boxplot of maximum sperm tail length (µm) for species in the divisions (H) Hydromys, (U) Uromys, (P) Pogonomys, (M) Mallomys, and (R) Rattus.
Figure 2 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 2. Boxplot showing maximum numbers of fetuses across the species in the divisions (H) Hydromys, (U) Uromys, (P) Pogonomys, (M) Mallomys, and (R) Rattus.
Figure 1 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 1. Boxplot showing nipple numbers for species in the divisions (H) Hydromys, (U) Uromys, (P) Pogonomys, (M) Mallomys, and (R) Rattus.
Figure 5 in Reproductive Biology of the Mice and Rats (Family Muridae) in New Guinea-Diversity and Evolution
Figure 5. Light micrographs of spermatozoa from (a) Leptomys elegans, (b) Melomys rufescens, (c) Pogonomys championi, (d) Pogonomys loriae, (e) Abeomelomys sevia, (f) Anisomys imitator, and (g) Rattus steini. Scale bars a = 4 µm, b–g = 5 µm.
Figure 5 in A new species of Maldivea Gerlach, 1962 (Nematoda, Oxystominidae) from Felidhoo atoll (Maldives, Indian Ocean) and an emended diagnosis of the sub-family and genus
Figure 5. World distribution of the species belonging to the subfamily Paroxystomininae De Coninck, 1965.
Figure 4 in A new species of Maldivea Gerlach, 1962 (Nematoda, Oxystominidae) from Felidhoo atoll (Maldives, Indian Ocean) and an emended diagnosis of the sub-family and genus
Figure 4. Light micrographs of the male of Maldivea complexa n. sp. A,B) Detail of the buccal cavity, C) Detail of amphideal fovea, D) Copulatory apparatus, E) Precloacal sub-ventral pairs of short and stout setae close to the cloacal opening, F) Detail of the precloacal sub-ventral pairs of short and stout setae in the elevation of the cuticle, G) Details of the post-cloacal setae and tail tip. Scale bars: A-B: 5 µm, C,E: 10 µm; D, F,G: 20 µm.
Figure 3 in A new species of Maldivea Gerlach, 1962 (Nematoda, Oxystominidae) from Felidhoo atoll (Maldives, Indian Ocean) and an emended diagnosis of the sub-family and genus
Figure 3. Drawings of the male of Maldivea complexa n. sp. A) Detail of the anterior end of the male. B) Detail of the amphideal fovea of the male. C) Detail of the copulatory apparatus and caudal region. Scale bar: A: 10 µm, B: 50 µm.
Figure 8 in On two new or interesting species of the family Niphargidae from Greece and Croatia (Contribution to the knowledge of the Amphipoda 286)
Figure 8. Niphargus impexus, sp. n., Iraklion, Crete Island, Greece, female 9.2 mm: A pereopod 5; B-C pereopod 6; D- E-F pereopod 7.
Figure 5 in On two new or interesting species of the family Niphargidae from Greece and Croatia (Contribution to the knowledge of the Amphipoda 286)
Figure 5. Niphargus impexus, sp. n., Iraklion, Crete Island, Greece, male 9.8 mm: A coxa 5; B-C-D pereopod 6; E-F-G pereopod 7.
Figure 2 in On two new or interesting species of the family Niphargidae from Greece and Croatia (Contribution to the knowledge of the Amphipoda 286)
Figure 2. Niphargus impexus, sp. n., Iraklion, Crete Island, Greece, male 9.8 mm: A mandible palpus, outer face; B distal mandible palpus article, inner face with B-setae; C right mandible incisor, lacinia mobilis and rakers; D left mandible incisor and lacinia mobilis; E maxilliped; F peduncle of pleopod 1; G peduncle of pleopod 2; H peduncle of pleopod 3; I= uropod 3. Female 9.2 mm: J third palpus article of mandible, inner face with B, D and E-setae.
Figure 1 in On two new or interesting species of the family Niphargidae from Greece and Croatia (Contribution to the knowledge of the Amphipoda 286)
Figure 1. Niphargus impexus, sp. n., Iraklion, Crete Island, Greece, male 9.8 mm: A antenna 1; B antenna 2; C labium; D maxilla 1; E maxilla 2; F epimeral plates 1-3; G telson.
Figure 7 in On two new or interesting species of the family Niphargidae from Greece and Croatia (Contribution to the knowledge of the Amphipoda 286)
Figure 7. Niphargus impexus, sp. n., Iraklion, Crete Island, Greece, female 9.2 mm: A inner plate of maxilla 1; B pereopod 3; C coxa 4; D epimeral plates 1-3; E peduncle of pleopod 1; F peduncle of pleopod 2; G peduncle of pleopod 3.
Figure 4 in On two new or interesting species of the family Niphargidae from Greece and Croatia (Contribution to the knowledge of the Amphipoda 286)
Figure 4. Niphargus impexus, sp. n., Iraklion, Crete Island, Greece, male 9.8 mm: A labrum; B head; C-D pereopod 3; E-F pereopod 4; G urosome with uropods 1-2.
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.