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.
213
datasets available to search
ShareScore release 0.9.0
Dataset results
213 results for “ontogenetic changes”
Figure 1 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 1. Body mass (◆) and total length (■) of Japanese flounder during larval and juvenile development related to days after hatching. Values are given as the mean ± SD. Each value is obtained from 35 individuals.
Figure 2 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 2. Instantaneous growth rate (A) and absolute growth rate (B) of body mass (◆) and total length (v) in Japanese flounder during larval and juvenile development related to days after hatching. Values are given as the mean ± SD. Each value is obtained from 35 individuals.
Figure 4 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 4. Changes in DNA content (■) and DNA concentration (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 7 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 7. Diel variation of the RNA/DNA ratio in the fed () and starved (■) Japanese flounder larvae during the 48-h period. Values are given as the mean ± SD. Each value is obtained from 15 individuals. The dark line means the dark time.
Figure 3 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 3. Changes in protein content (■) and protein concentration (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 6 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 6. Changes in protein/DNA (■) and RNA/DNA (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 5 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 5. Changes in RNA content (■) and RNA concentration (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 8 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 8. Changes in RNA/DNA ratios of Japanese flounder exposed to different starved-refeeding treatments from 20 to 27 days after hatching: (A) fed (control treatment), (B) 1-day starved, (C) 2-day starved, (D) 3-day starved, (E) 4-day starved. Values are given as the mean ± SD. Each value is obtained from 10 individuals. Dark symbols mean feeding days and empty symbols mean starved days.
Fig. 5 in First Specimen-based Record of Ammolabrus dicrus (Perciformes: Labridae) from Japanese Waters, with Notes on Morphological Ontogenetic Changes and Geographic Variation
Fig. 5. Semi-schematic illustration of head of Ammolabrus dicrus, showing positions of cephalic sensory canals (KAUM–I. 99313, 21.4 mm SL). Scale bar 1 mm.
Fig. 4 in First Specimen-based Record of Ammolabrus dicrus (Perciformes: Labridae) from Japanese Waters, with Notes on Morphological Ontogenetic Changes and Geographic Variation
Fig. 4. Relationships of (A) number of gill rakers, (B) body depth, (C) caudal-peduncle length, and (D) orbit diameter to SL in Japanese (stars) and Hawaiian (circles) specimens of Ammolabrus dicrus. Open circle indicates holotype.
Fig. 2 in First Specimen-based Record of Ammolabrus dicrus (Perciformes: Labridae) from Japanese Waters, with Notes on Morphological Ontogenetic Changes and Geographic Variation
Fig. 2. Ammolabrus dicrus from Taketomi Island, Yaeyama Islands, Ryukyu Islands, Japan. A, specimen photograph (KAUM–I. 99314, 18.4 mm SL); B, underwater photograph of same individual as in A, 12 m; photo by T. Uchida.
Fig. 1 in First Specimen-based Record of Ammolabrus dicrus (Perciformes: Labridae) from Japanese Waters, with Notes on Morphological Ontogenetic Changes and Geographic Variation
Fig. 1. Underwater photograph of a small school of Ammolabrus dicrus at a depth of 12 m off Taketomi Island, Yaeyama Islands, Ryukyu Islands, Japan; photo by K. Sodo.
Fig. 3 in Distribution Range Extensions of Parapercis bicoloripes and P. diplospilus (Perciformes: Pinguipedidae) in the South China Sea and the Adjacent Waters, with Notes on Ontogenetic Changes in P. bicoloripes
Fig. 3. Ontogenetic changes in relationship of snout length (circles) and fleshy orbit diameter (triangles) as percentage of standard length to standard length (mm) in Parapercis bicoloripes.
Fig. 2 in Distribution Range Extensions of Parapercis bicoloripes and P. diplospilus (Perciformes: Pinguipedidae) in the South China Sea and the Adjacent Waters, with Notes on Ontogenetic Changes in P. bicoloripes
Fig. 2. Distribution of Parapercis bicoloripes (triangles) and P. diplospilus (circles). Closed and open symbols indicate previously known and new records, respectively.
Fig. 1 in Distribution Range Extensions of Parapercis bicoloripes and P. diplospilus (Perciformes: Pinguipedidae) in the South China Sea and the Adjacent Waters, with Notes on Ontogenetic Changes in P. bicoloripes
Fig. 1. Fresh specimens of Parapercis bicoloripes from Malaysia (A–B) and the Philippines (C). A, KAUM–I. 79754, 136.0 mm SL, off Kuala Terengganu; B, KAUM–I. 16935, 120.4 mm SL, off Kuala Terengganu; C, KAUM–I. 69435, 66.1 mm SL, off Miagao, Iloilo, Panay Island.
Fig. 1 in Scorpaena dabryi, a Junior Synonym of Scorpaena miostoma, with Notes on Morphological Ontogenetic Changes (Teleostei: Scorpaenidae)
Fig. 1. Photographs of Scorpaena miostoma. A, lectotype of S. dabryi (MNHN 6882, male, 75.5 mm SL); B, paralectotype of S. dabryi (MNHN 6882, 71.0 mm SL); C, holotype of S. miostoma (BMNH 1879.5.14.235, 106.4 mm SL).
Fig. 3 in Scorpaena dabryi, a Junior Synonym of Scorpaena miostoma, with Notes on Morphological Ontogenetic Changes (Teleostei: Scorpaenidae)
Fig. 3. Life stages of Scorpaena miostoma. A, KAUM–I. 71264, male, 43.8 mm SL; B, KAUM–I. 25862, 62.3 mm SL; C, KAUM–I. 71449, male, 81.5 mm SL; D, KAUM–I. 30796, 108.2 mm SL; E, KAUM–I. 10014, male, 124.4 mm SL.
FIGURE 7 in Two new species of Knodus (Characidae: Stevardiinae) from the upper rio Tocantins basin, with evidence of ontogenetic meristic changes
FIGURE 7 | Knodus obolus, paratypes. Ontogenetic and polymorphic variation of the body shape and colour patterns. All from the ribeirão Dois Irmãos drainage, upper Tocantins basin in Pirenópolis, Goiás State, Brazil. A. NUP 22668, 56.9 mm SL. B. NUP 22668, 53.2 mm SL. C. NUP 22668, 49.6 mm SL. D. NUP 22668, 45.0 mm SL. E. NUP 22668, 33.1 mm SL.
FIGURE 2 in Two new species of Knodus (Characidae: Stevardiinae) from the upper rio Tocantins basin, with evidence of ontogenetic meristic changes
FIGURE 2 | Knodus rufford, holotype, NUP 22661, 35.4 mm SL, ribeirão Dois Irmãos, tributary to the rio do Peixe, tributary to the rio das Almas, tributary to the rio Maranhão, tributary to the rio Tocantins, Municipality of Pirenópolis, Goiás State, Brazil.
FIGURE 10 in Two new species of Knodus (Characidae: Stevardiinae) from the upper rio Tocantins basin, with evidence of ontogenetic meristic changes
FIGURE 10 | Knodus aff. breviceps from the rio das Almas basin, upper Tocantins basin (collected in syntopy with K. obolus and K. rufford). A. NUP 22666, 55.3 mm SL. B. NUP 22662, 42.0 mm SL. C. NUP 22665, 28.2 mm SL. D. NUP 22665, 23.9 mm SL.
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.