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.
173
datasets available to search
ShareScore release 0.7.1
Dataset results
173 results for “Syngnathidae”
Fig. 1 in A New Genus and Species of Pygmy Pipehorse from Taitokerau Northland, Aotearoa New Zealand, with a Redescription of Acentronura Kaup, 1853 and Idiotropiscis Whitley, 1947 (Teleostei, Syngnathidae)
Fig. 1. CyliX tupareomanaia. (A) AIM MA122274, female, holotype shortly after death, 31.4 mm SL; Waiatapaua Bay, Whangaruru, Northland, New Zealand (photograph © Auckland Museum). (B) NMNZ P.056154, female, paratype, shortly after death, 35.5 mm SL; Cavalli Islands, Northland, New Zealand (photograph © Irene Middleton).
Fig. 8 in A New Genus and Species of Pygmy Pipehorse from Taitokerau Northland, Aotearoa New Zealand, with a Redescription of Acentronura Kaup, 1853 and Idiotropiscis Whitley, 1947 (Teleostei, Syngnathidae)
Fig. 8. Lateral view of preserved specimens of Acentronura spp. redescribed in this study. (A) A. breViperula, CAS 247135, female, 40.1 mm SL. (B) A. gracilissima, CAS-SU 6681, male, 70.4 mm SL. (C) A. tentaculata, CAS 247139, male, 50.8 mm SL. (D) A. tentaculata, CAS 247139, female, 53.9 mm SL.
Fig. 6 in A New Genus and Species of Pygmy Pipehorse from Taitokerau Northland, Aotearoa New Zealand, with a Redescription of Acentronura Kaup, 1853 and Idiotropiscis Whitley, 1947 (Teleostei, Syngnathidae)
Fig. 6. CyliX tupareomanaia in situ. (A) AIM MA122274, female, holotype, Waiatapaua Bay, Whangaruru, Northland, New Zealand, 12 m depth (photograph © Shane Housham). (B) Waiatapaua Bay, Whangaruru, Northland, New Zealand, 12 m depth (photograph © Shane Housham). (C) Waiatapaua Bay, Whangaruru, Northland, New Zealand, 12 m depth (photograph © Richard Smith). (D) Waiatapaua Bay, Whangaruru, Northland, New Zealand, 12 m depth (photograph © Irene Middleton). (E) Waiatapaua Bay, Whangaruru, Northland, New Zealand, 12 m depth (photograph © Irene Middleton). (F) Poor Knights Islands, Northland, New Zealand, at 10 m depth (photograph © Kent Erickson).
Fig. 5 in A New Genus and Species of Pygmy Pipehorse from Taitokerau Northland, Aotearoa New Zealand, with a Redescription of Acentronura Kaup, 1853 and Idiotropiscis Whitley, 1947 (Teleostei, Syngnathidae)
Fig. 5. µCT scan of the ventral aspect of first trunk ring of CyliX tupareomanaia, NMNZ P.046322, male, paratype, 55.5 mm SL, in ventral aspect highlighting positions of large medioventral conical spines on the cleithral symphysis and the first trunk ring between the pectoral-fin bases. Abbreviations: CL, cleithral spines; CSS, medioventral conical spine on the cleithral symphysis; MVFTRS, medioventral first trunk ring spine between the pectoral-fin bases; PLS, posterolateral spine on pectoral-fin base.
FIGURE 4 in Population structure of the seahorse Hippocampus reidi (Syngnathiformes: Syngnathidae) in a Brazilian semi-arid estuary
FIGURE 4 | Proportion of color patterns (A) and holdfast use (B) of Hippocampus reidi in the Pacoti River estuary, Ceará, Brazil, between December 2017 and November 2018.
FIGURE 3 in Population structure of the seahorse Hippocampus reidi (Syngnathiformes: Syngnathidae) in a Brazilian semi-arid estuary
FIGURE 3 | Spatial variation in the proportion of pregnant males of Hippocampus reidi along the salinity gradient in the Pacoti River estuary, Ceará, Brazil, between December 2017 and November 2018. Y = pregnant male record, N = non-pregnant male record.
FIGURE 2 in Population structure of the seahorse Hippocampus reidi (Syngnathiformes: Syngnathidae) in a Brazilian semi-arid estuary
FIGURE 2 | Temporal variation of environmental variables: (A) salinity and (B) water transparency (cm), and Hippocampus reidi population variables: (C) population density (ind.m-2), (D) proportion of pregnant males (Y = pregnant male record, N = non-pregnant male record) and (E) individual height (cm), in the Pacoti River estuary, Ceará, Brazil, between December 2017 and November 2018. The months of the rainy season are highlighted in blue.
FIGURE 1 in Population structure of the seahorse Hippocampus reidi (Syngnathiformes: Syngnathidae) in a Brazilian semi-arid estuary
FIGURE 1 | Geographic location of the Pacoti River estuary, Ceará, Brazil (A, B), indicating Hippocampus reidi sampling locations (A to K) (C).
Figure 5 in A new species of freshwater pipefish (Teleostei: Syngnathidae: Coelonotus) from Papua New Guinea
Figure 5. – Distributions of the species of Coelonotus in the Indo-Pacific: Coelonotus argulus (in blue), Coelonotus leiaspis (in green), Coelonotus biocellatus (in red) and Coelonotus kaipuae n. sp. (in yellow). Type localities: C. argulus (■), C. leiaspis (■), C. biocellatus (■) and C. kaipuae n. sp. (■). Sampled localities in black. PNG: Papua New Guinea.
Figure 4 in A new species of freshwater pipefish (Teleostei: Syngnathidae: Coelonotus) from Papua New Guinea
Figure 4. – Photo of type locality of Coelonotus kaipuae n. sp.. Gavuvu river, West New Britain, Papua New Guinea (© Lord C.).
Figure 1 in A new species of freshwater pipefish (Teleostei: Syngnathidae: Coelonotus) from Papua New Guinea
Figure 1. – Bayesian tree of the cytochrome c oxidase subunit (COI – 564 bp) for sequenced specimens of Coelonotus. Numbers at each node represent posterior probabilities. Outgroups are represented by Hippichthys heptagonus. PNG: Papua New Guinea.
Figure 2. – A in A new species of freshwater pipefish (Teleostei: Syngnathidae: Coelonotus) from Papua New Guinea
Figure 2. – A: Diagram of the head of Coelonotus kaipuae n. sp. B: Diagram of the lateral trunk (in red) and tail (in blue) ridges of Coelonotus kaipuae n. sp.
FIGURE 4 in Partial characterization of digestive proteases in juveniles of Microphis brachyurus (short-tailed pipefish) (Syngnathiformes: Syngnathidae)
FIGURE 4 | SDS-PAGE zymogram of alkaline digestive proteases of short-tailed pipefish (Microphis brachyurus) juveniles: Molecular weight marker (MWM), rabbit phosphorylase B (97.4 kDa), bovine serum albumin (66.2 kDa), ovalbumin (42.7 kDa), carbon anhydrase (31.0 kDa) and lysozyme (14.4 kDa); control (without inhibitor); inhibitors were the same as in Fig. 3.
FIGURE 3 in Partial characterization of digestive proteases in juveniles of Microphis brachyurus (short-tailed pipefish) (Syngnathiformes: Syngnathidae)
FIGURE 3 | Residual activity (%) of digestive proteases using several inhibitors on multienzyme extracts of short-tailed pipefish (Microphis brachyurus) juveniles. Alkaline proteases with no inhibitor (Alk control), tosylphenylanylchloromethyl ketone (TPCK), phenanthroline (PHEN), ethyl-diamine tetra-acetic acid (EDTA), tosyllysyl- chloromethyl ketone (TLCK), ovalbumin (OVO), soybean trypsin inhibitor (SBT1), phenyl methyl sulphonyl fluoride (PMSF), acidic proteases with no inhibitor (Acid control), pepstatin A (mean ± SD, n = 3). Columns with different letters represent significant differences (p <0.05).
Figure 3 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
Figure 3. – Distributional map of Centrogenys vaigiensis. The star indicates locality of FAKU 103752 (Mauritius). Shaded area indicates previously recorded distributional range.
Figure 2 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
Figure 2. – Head of Centrogenys vaigiensis [FAKU 103752, 73.7 mm SL, Mauritius]. Arrowheads indi- cate antrorse spines on preopercle margin.
Figure 1 in First record of the near threatened native seahorse Hippocampus reidi (Teleostei: Syngnathidae) in an ecosystem dominated by the invasive seagrass Halophila stipulacea in the Caribbean Sea
Figure 1. – Specimen of Hippocampus reidi Ginsburg, 1933, photographed in a dense Halophila stipulacea seagrass bed on the west coast of Martinique Island, on 9th June 2017.
Linked collectors and determiners for: Taxonomic review of the pipefish genus Pseudophallus Herald, with the description of a new species (Syngnathiformes: Syngnathidae).
Natural history specimen data linked to collectors and determiners held within, "Taxonomic review of the pipefish genus Pseudophallus Herald, with the description of a new species (Syngnathiformes: Syngnathidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/ff9ddcdc-1340-4533-ae1e-da83b895158c">https://bionomia.net/dataset/ff9ddcdc-1340-4533-ae1e-da83b895158c</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/ff9ddcdc-1340-4533-ae1e-da83b895158c">https://gbif.org/dataset/ff9ddcdc-1340-4533-ae1e-da83b895158c</a>. Formatted as a Frictionless Data package.
Fig. 2 in Assessing diet composition of seahorses in the wild using a non destructive method: Hippocampus reidi (Teleostei: Syngnathidae) as a study-case
Fig. 2. Feeding strategy diagram. Prey-specific abundance plotted against frequency of occurrence of prey items in the diet of the seahorse Hippocampus reidi (n = 280). Prey items: 1. Nematoda, 2. Copepoda, (Harpacticoida), 3. Caridae, 4. Copepoda (nauplii), 5. Copepoda (Calanoida), 6. Copepoda (Cyclopoida), 7. Caridae (chelipods), 8. Teleostei (Gobiidae), 9. Insecta (Hymenoptera), 10. Amphipoda (Gammaridae), 11. Teleostei (scales), 12. Polichaeta (larvae), 13. Amphipoda (Caprellidae), 14. Ostracoda, 15. Eggs (possibly of mollusks or crustaceans), 16. Polichaeta (Nereididae), 17. Brachyura (nauplii), 18. Insecta (Chironomidae), 19. Crustacea (larvae), 20. Gastropoda (larvae), 21. Bivalvia (larvae), 22. Caridae (zoea), 23. Isopoda, 24. Oligochaeta, 25. Foraminifera.
Fig. 1 in Assessing diet composition of seahorses in the wild using a non destructive method: Hippocampus reidi (Teleostei: Syngnathidae) as a study-case
Fig. 1. Mean values of induction (square) and recovery (lozenge) times of Hippocampus reidi (n = 242) in seconds (box = standard error; whisker = standard deviation). Reproduc- tive state: IM = immature, OF = ovipositor region flat, OB = ovipositor region bulging, B = brooding, NB = non-brooding. Sex: U = undetermined, F = female, M = male.
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.