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.
4,085
datasets available to search
ShareScore release 0.9.0
Dataset results
4,085 results for “Deep sea”
Figure 4 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters
Figure 4. Schematic diagram of Teuthowenia pellucida tentacle showing paired zig-zag sucker pattern on stalk, visible from Stage D onwards.
Figure 2 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters
Figure 2. Development of Teuthowenia pellucida eyes through ontogeny showing both anterior (right) and lateral (left) perspective. Eye presented from (A) stage A; (B) stage B; (C) stage C; (D) stage D; (E) stage E and F; (F) adult (anterior); (G) adult (ventral). Scale bar = 1 mm.
Figure 12 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters
Figure 12. Difference in visible rachis shape at anterior dorsal midline of (A) Teuthowenia; (B) Megalocranchia; (C) Liguriella (ML range: 17–29 mm).
Fig. 23. Phylogenetic hypothesis for the Halopterididae Millard, 1962 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 23. Phylogenetic hypothesis for the Halopterididae Millard, 1962. The species discussed in this study is highlighted in yellow, and the newly-produced sequence is in bold. Numbers at nodes represent BPP and BS, respectively, and are shown only when both BPP Ż 0.9 and BS Ż 75.
Fig. 18. Monostaechas fisheri Nutting, 1905 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 18. Monostaechas fisheri Nutting, 1905, morphotype with shallower hydrothecae and longer lateral nematothecae: patterns of branching. Slender lines represent cladia, thicker lines show primary, secondary or tertiary stems; dots correspond to the hydrothecae.
Fig. 15. A–B in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 15. A–B. Halopteris campanula (Busk, 1852), female (A) and male (B) gonothecae from samples MNHN-IK-2015-598 and MNHN-IK-2015-597, respectively. — C. Halopteris infundibulum Vervoort, 1966, possible female gonotheca, from sample MNHN-IK-2015-608. — D–E. Halopteris peculiaris Billard, 1913, female (D) and male (E) gonothecae, both from sample MNHN-IK-2015-609. Scale bar: 300 µm.
Fig. 14 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 14 (opposite page). A–D. Corhiza patula Galea sp. nov., from holotype MNHN-IK-2015-602, proximal portion of cladium (A); nematothecae: mesial (B), lateral (C), and from ahydrothecate internode (D). — E–J. Corhiza pauciarmata Ansín Agís et al., 2009, from sample MNHN-IK-2015-604, portion of cladium (E); nematothecae: mesial (F), lateral (G) and from ahydrothecate internode in lateral (H) and adaxial (I) aspects; cnidome (J). — K. Halopteris campanula (Busk, 1852), portion of cladium from sample MNHN-IK-2015-597. — L–M. Halopteris infundibulum Vervoort, 1966, cladial hydrotheca in lateral (L) and frontal (M) aspects, both from sample MNHN-IK-2015-608. — N–P. Halopteris peculiaris Billard, 1913, proximal portion of cladium seen laterally (N); single (O) or paired (P) lateral nematothecae associated to cauline hydrothecae; all from sample MNHN-IK-2015-609. Scale bars: A, E = 500 µm; B–D, F–I, O–P = 100 µm; J = 10 µm; K–N = 300 µm
Fig. 21 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 21 (opposite page). Phylogenetic hypothesis for the Aglaopheniidae Marktanner-Turneretscher, 1890. Species discussed in this study are highlighted in yellow. Newly produced sequences are in bold. Numbers at nodes represent Bayesian posterior probabilities (BPP) and maximum likelihood bootstrap supports (BS), respectively, and are shown only when both BPP Ż 0.9 and BS Ż 75.
Fig. 10 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 10 (opposite page). A. Schizoplumularia elegans Ansín Agís et al., 2016, monosiphonic portion of a branch with proximal part of a cladium, from sample MNHN-IK-2015-548. — B–K. Schizoplumularia helicoidalis sp. nov., portion of stem showing fate of component tubes (B); portion of branch with five successive cladial apophyses and proximal part of a cladium (C); portions of cladia from material other than the holotype (D–E); detail of cladial apophysis (F); cladial internode with hydrotheca and its associated nematothecae (G); nematothecae of stem (H) and of cladial intersegment in adaxial (I) and lateral (J) views; gonotheca from material not belonging to the type (K); B–C, F–J from the holotype, MNHN-IK-2015-610; D–E, K from sample MNHN-IK-2015-596. Scale bars: A, C–E = 300 µm; B = 1 mm; F–K = 100 µm
Fig. 20 in Plumularioid hydroids (Cnidaria: Hydrozoa) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program
Fig. 20 (opposite page). Thamnopteros uniserius Galea gen. et sp. nov., portion of fascicled stem giving rise laterally to a Halopteris-like branch, of which only the proximalmost part, showing the prosegment, is depicted (A); more distal portion of another branch, note slight change in the hydrothecal shape (the arrow indicates a cladial apophysis) (B); two cauline hydrothecae seen laterally, to show variation in the length of the lateral nematothecae (C–D); cladial hydrothecae seen laterally (E) and frontally (F), note differences in the size of the lateral nematothecae belonging to each pair; detail of the hydrothecal axil (G); nematothecae: mesial (H), of the component tubes of the fascicled stem (I), and from above the cauline hydrothecae (J); gonotheca (K); all from sample MNHN-IK-2015-611. Scale bars: A–B = 500 µm; C–F = 200 µm; G–J = 100 µm; K = 300 µm.
NACLIM - Fluxes: (DWBC) Labrador Sea Deep Western Boundary Current transport at 53° N
<p><strong>Last update: 17 October 2014</strong></p> <p><strong>Data set:</strong> Labrador Sea Deep Western Boundary Current (DWBC) transport at 53° N </p> <p><strong>Description:</strong> 5-day averages of DWBC along-shore volume transport as measured at the 53° N mooring array, per water mass in depth layers</p> <p><strong>Period:</strong> July 1997 – April 2012</p> <p><strong>Location:</strong> 53° 0′ N 51° 0′ W </p> <p><strong>Instruments:</strong> Moored rotor current meters (RCM); acoustic current meters (ACM); acoustic Doppler current profilers (ADCP) </p> <p><strong>Variables:</strong> NADW, NEADW, DSOW, LNADW - along-shore volume transport for each water mass (LSW transport may be derived as described in the readme-file)</p> <p><strong>Source: </strong>Johannes Karstensen, Jürgen Fischer and Rainer Zantopp (GEOMAR)</p> <p><strong>About the data: </strong></p> <p>LabSea53N_DWBC.dat (ASCII): This is the updated DWBC transports at 53N in ascii form, including all available data from July 1997 to April 2012</p> <p>LabSea53N_DWBC.nc (netCDF)</p> <p>Plot (JPEG): The export of North Atlantic Deep Water (NADW) from the moored array at the exit of the Labrador Sea. Data at 5day resolution (red and green lines), for 90day low-pass time series (black), and as annual mean transports (blue bars) – see legend in the graph. Transport statistics also included.</p>
FIGURE 3 in Crossota millsae (Cnidaria: Trachymedusae: Rhopalonematidae), a new species of viviparous hydromedusa from the deep sea off California and Hawaii
FIGURE 3. Crossota millsae, sp. nov. a) Two of the juvenile paratype specimens representing different stages of early development, scale bar = 2.5 mm. b) Two of the juvenile paratype specimens representing later stages of development, same scale bar as in Fig 3 a. c) Abscission zone at base of tentacles. ABS = abscission point, RC = ring canal, YIP = yellow iridescent pigment. d) Scanning electron micrograph of spermatids from testes of the male specimen shown in Fig. 1 b. Three size classes of spermatids are noted, A ~ 10 µm, B ~ 5 µm and C ~ 2 µm. The smallest spermatids have developing flagella. Scale bar = 10 µm.
FIGURE 2 in Crossota millsae (Cnidaria: Trachymedusae: Rhopalonematidae), a new species of viviparous hydromedusa from the deep sea off California and Hawaii
FIGURE 2. In situ video frame of Crossota millsae sp. nov. taken off California from the Monterey Bay Aquarium Research Institute’s ROV Tiburon. This is a female specimen with developing juveniles.
FIGURE 1 in Crossota millsae (Cnidaria: Trachymedusae: Rhopalonematidae), a new species of viviparous hydromedusa from the deep sea off California and Hawaii
FIGURE 1. Crossota millsae, sp. nov. a) Lateral view of female specimen. Scale bar = 9 mm. b) Lateral view of male paratype specimen. Note the exumbrellar furrows. Scale bar = 5 mm. c) Oral view of female shown in Fig 1 a with developing juveniles. Scale bar = 9 mm. d) Aboral view of female with developing juveniles. Scale bar = 10 mm.
FIGURE 1. Chiridota heheva new species. Approximately 4 in Chiridota heheva, new species, from Western Atlantic deepsea cold seeps and anthropogenic habitats (Echinodermata: Holothuroidea: Apodida)
FIGURE 1. Chiridota heheva new species. Approximately 4 individuals in situ near whitish bacterial mats (?) at Florida Escarpment seep site, eastern Gulf of Mexico, 3,270 meters. Alvin Dive 1343. Approximate diameter of body 5 mm. Photo, S. Golubic.
FIGURE 3. A – C, E – J in Chiridota heheva, new species, from Western Atlantic deepsea cold seeps and anthropogenic habitats (Echinodermata: Holothuroidea: Apodida)
FIGURE 3. A – C, E – J, Chiridota heheva new species; D, Chiridota laevis (Fabricius). A, Left ventral radial piece from calcareous ring. Note absence of perforation for radial nerve. Length of piece 1. 9 mm. B, Right ventral interradial piece from calcareous ring; length of piece 1. 6 mm. C, Bipartite right dorsal radial piece from calcareous ring. Note absence of perforation for radial nerve. Length of piece 2. 7 mm. D, Chiridota laevis (Fabricius), bipartite right dorsal radial piece from calcareous ring. Note perforation for radial nerve. Length of piece mm. 1.6 mm. E, Rods from tentacles. Length of longest rod 177 µm. F, Inner surface of wheel from wheel papilla. Diameter of wheel 186 µm. G, Outer surface of wheel from wheel papilla. Diameter of wheel 154 µm. H, Three wheels from wheel papillae, two showing inner surface, one showing outer surface. Largest wheel abnormal in having teeth on margin of inner rim. Diameter of largest wheel 184 µm. I, Wheel in lateral view. Diameter of wheel 132 µm. J, Wheel in slightly oblique view. Diameter of wheel 190 µm.
FIGURE 2. Chiridota heheva new species. A in Chiridota heheva, new species, from Western Atlantic deepsea cold seeps and anthropogenic habitats (Echinodermata: Holothuroidea: Apodida)
FIGURE 2. Chiridota heheva new species. A, At Bathymodiolus heckeri mussel beds, Blake Ridge, closeup view showing anterior end of body with white spots (wheel papillae), and extended tentacles. Note fingerlike digits forming a fringe around tentacle terminal disc. Approximate diameter of tentacle stem 1 mm. From Van Dover et al., 2003, with permission. B, One individual at Bathymodiolus heckeri mussel beds, Blake Ridge, showing conspicuous white spots (wheel papillae) against bluish ground color of body wall. Approximate diameter of body 5 mm. Shrimp at right center is Alvinocaris sp. From Van Dover et al., 2003, with permission. C, At Central America wreck showing conspicuous white spots (wheel papillae) against bluish ground color of body wall. Image taken from videotape, Charles E. Herdendorf. Size of specimen unknown. D, At Central America wreck, showing extended feeding tentacles with conspicuous, discrete digits. Size of specimen unknown. Image taken from videotape, Charles E. Herdendorf. E, Oral field with 12 tentacles in a partially contracted state. Note absence of a “ ventral gap ” between tentacles. Long axis of mouth is 2 mm. F, Closeup view of contracted tentacles showing infolded digits. G, Partially contracted tentacle showing discrete digits. Approximate length of digits 1. 5 mm.
FIGURE 4 in First report of two deep-sea shrimps of the genus Acanthephyra A. Milne-Edwards, 1881 (Crustacea: Decapoda: Acanthephyridae) from southwestern Atlantic
FIGURE 4. Geographic distribution of Acanthephyra armata A. Milne-Edwards, 1881 b. Black circles = previous records; star = new record.
FIGURE 2 in First report of two deep-sea shrimps of the genus Acanthephyra A. Milne-Edwards, 1881 (Crustacea: Decapoda: Acanthephyridae) from southwestern Atlantic
FIGURE 2. Geographic distribution of Acanthephyra acanthitelsonis Spence Bate, 1888 in the Atlantic Ocean. Black circles = previous records; star = new record.
FIG. 5 in At the bottom of the deep blue sea: a new wood-boring bivalve (Mollusca, Pholadidae, Xylophaga) from the Cape Verde Abyssal Plain (subtropical Atlantic)
FIG. 5. — Incurrent siphonal opening of Xylophaga alexisi n. sp., SEM. Note absence of cirri. Scale bar: 30 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.