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Figure 2 in Mating and ejaculate allocation pattern in the kelp crab Taliepus dentatus (Decapoda: Epialtidae)
Figure 2. Box plot of seasonal vasosomatic index (VSI) of Taliepus dentatus from Los Molinos Bay, Chile. Boxes: interquartile range of the data (first quartile, median and third quartile). Whiskers: the values that extend to 1.5 times the interquartile range. Circles: outliers. Letters indicate significant differences (p <0.05) (R v 3.4).
Figure 3 in Population biology of the freshwater shrimp Atya scabra (Leach, 1816) (Crustacea: Decapoda) in São Francisco River, Brazil: evidence from a population at risk of extinction
Figure 3. Atya scabra (Leach, 1816). Size-frequency distribution of carapace length (mm) of the male and female shrimp sampled in São Francisco River, Sergipe, Brazil.
Figure 9 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 9. Chondracanthus kabatai sp. n. from Zenopsis conchifer Lowe. A, B. Holotype, female, dorsal and ventral view. C. Paratype, female (ZSI/WGRC/IR/INV/11732), dorsal view, D. Paratype, female (ZSI/WGRC/IR/INV/11729), dorso-lateral view.
Figure 1 in Population biology of the fiddler crab Uca maracoani (Crustacea, Ocypodidae) inhabiting an impacted mangrove area on the southern coast of São Paulo state, Brazil
Figure 1. Proportion of females (white bars) and males (black bars) of Uca maracoani by (A) Month and (B) Crab size (CW in mm).
Figure 6 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 6. Acanthochondria krishnai sp. n., non-type male from Uranoscopus guttatus Cuvier. A. Habitus lateral view. B. Antennule. C. Antenna. D. Mandible. E. Maxillule. F. Maxilla. G. Maxilliped. H. Leg 1. I. Leg 2. J. Lateral view of genito-abdomen. K. Ventral view of genito-abdomen.
Figure 7. A, B in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 7. A, B. Site of attachment of Chondracanthus kabatai sp. n. (arrows) on its host fish Zenopsis conchifer Lowe.
Figure 5 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 5. Acanthochondria krishnai sp. n., non-type male from Uranoscopus guttatus Cuvier. A. Habitus lateral view. B. Antennule. C. Antenna.
Figure 4 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 4. Seasonal predicted mean cephalothorax length (CL) by depth stratum for males, non-ovigerous and ovigerous females of Plesionika edwardsii in the Azorean region for the period 1999–2000. Light-colored symbols represent raw data. Detailed parameter estimates are in Tab. S4.
Figure 1 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 1. Sampling areas of Plesionika edwardsii in the mid-North Atlantic Ocean, Azorean region (ICES Subdivision 10a2) between 1999 and 2000. Orange dots represent each site sampled by a trap.
Figure 4 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 4. Acanthochondria krishnai sp. n., paratype, female from Uranoscopus guttatus Cuvier. A. Mandible. B. Maxillule. C. Maxilla. D. Maxilliped. E. Maxilliped apex. F. Leg 1. G. Leg 2. H, I. Genito-abdomen with rami, ventral and ventro-lateral views. J. Rami.
Figure 2 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 2. Acanthochondria krishnai sp. n., holotype, female from Uranoscopus guttatus Cuvier. A. Dorsal view. B. Ventral view. C, D. Cephalon, dorsal and ventral views. E. Antennule. F. Antenna.
Figure 10 in A new Northeast Asian Lynceus (Crustacea: Branchiopoda: Laevicaudata) with uniquely modified thoracopods and an evaluation of DNA barcoding for clam shrimp species identification
Figure 10. Genetic distances and DNA barcoding gaps in clam shrimps. A. Stacked histogram of p-distances (yellow) and K2P genetic distances (blue) between pairs of COX1 sequences available in GenBank (accession date: 11/11/2018) for every suborder of clam shrimp (Laevicaudata, Spinicaudata, and Cyclestherida). The presence of a DNA barcoding gap is highlighted with a dashed vertical line. B. Saturation plot showing the strong correlation between p-distances and corrected genetic distances (Kimura 2-parameter).
Figure 1 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 1. Acanthochondria krishnai sp. n., female from Uranoscopus guttatus Cuvier. A, B. Dorsal view. C. Ventral view.
Figure 2 in Population biology of the freshwater shrimp Atya scabra (Leach, 1816) (Crustacea: Decapoda) in São Francisco River, Brazil: evidence from a population at risk of extinction
Figure 2. Map of Brazil indicating the São Francisco River watershed. Inset: sampling site (black circle) and the region of the Xingó Reservoirs (white circle). Legend: MG–Minas Gerais; BA–Bahia; SE–Sergipe; AL–Alagoas; PE–Pernambuco.
Figure 2 in Occurrence of Anthalona neotropica Sousa, Elmoor-Loureiro and Debastiani-Júnior, 2015 (Crustacea: Cladocera: Chydoridae) in Bahia State, Brazil
Figure 2. Anthalona neotropica Sousa, Elmoor-Loureiro and Debastiani-Júnior, 2015. A, Habitus, specimen from Jequitinhonha River. B, Habitus, specimen from Una River. C–E, Post-abdomen (arrow indicating the lateral fascicles). F, Labral keel and antenna. G, Spine on the first segment of endopod of antenna. H, First trunk limb, arrows showing the IDL setae. I, Head pores. mp: main pores, lp: lateral pore. Scale bars = 100 µm (A, B) or 10 µm (C–I).
Figure 3 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 3. Acanthochondria krishnai sp. n., non-type female from Uranoscopus guttatus Cuvier. A. Cephalon ventral view showing cephalic appendages. B. Antennule (arrow). C. Antennules (arrows). D. Cephalic appendages. E. Leg 1. F. Leg 2. G–J. Genitoabdomen. G. Lateral view with rami. H. Ventral view with rami. I. Dorsal view with male. J. With rami. (a1- antennule, a2- antenna, mxp- maxilliped, max- maxilla; L1- leg 1, L2- leg 2, m- male, r- rami).
Figure 6 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 6. Sex ratio of Plesionika edwardsii by size class in the Azorean region during the period 1999–2000.
Figure 3 in Unraveling distributional patterns and life-history traits of a deep-water shrimp Plesionika edwardsii (Decapoda, Pandalidae) under unexploited virgin conditions: a benchmark for fisheries management
Figure 3. Size frequency distribution of males, non-ovigerous and ovigerous females Plesionika edwardsii in the Azorean region during the period 1999-2000.
Figure 14 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 14. Chondracanthus kabatai sp. n., paratype male from Zenopsis conchifer Lowe. A. Habitus, lateral view. B. Antennule. C. Antenna. D. Mandible. E. Maxillule. F. Maxilla. G. Maxilliped. H. Leg 1. I. Leg 2. J. Lateral view of genito-abdomen. K. Rami.
Figure 9. Lynceus grossipedia n in A new Northeast Asian Lynceus (Crustacea: Branchiopoda: Laevicaudata) with uniquely modified thoracopods and an evaluation of DNA barcoding for clam shrimp species identification
Figure 9. Lynceus grossipedia n. sp., male, light microscopy of right side thoracopods (unmodified) (paratype, NHMD-616086). A. Thoracopods I (male clasper) and II, seen from posterior. B. Higher magnification of clasper. C–K. Thoracopods III–X, seen from anterior; all of "regular" Lynceus type (= unmodified). Arrows indicate broken/hidden parts.
ScienceDex guides
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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.