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.
1,552
datasets available to search
ShareScore release 0.7.1
Dataset results
1,552 results for “moorings”
Data for Mooring Impacts on Zostera marina Meadows and Associated Epifauna in Nantucket Harbor, Massachusetts, USA
<p>Submitted in fulfillment of a 2015 Nantucket Biodiversity Initiative grant.<br> <br> Excerpt from thesis abstract: "To explore the connections between mooring scarring, the surrounding seagrass meadow condition and epifaunal community, in the second part of this thesis I measured 30 mooring scars to determine average scar size. To explore any potential "halo" effect around mooring scars for seagrass or epifauna and to seek any difference in epifaunal community between mooring and reference sites I also sampled paired sites at eight locations in Nantucket Harbor, Massachusetts three times each in the summer of 2015. Each location consisted of a meadow site actively experiencing mooring scarring and a reference site without moorings. My conservative sampling methods of the 30 sampled mooring scars found scars to average 21.1m2. Across my paired sites, seagrass was found to have lower cover and lower canopy height in mooring versus reference sites. Seagrass cover and canopy height were lower in the first few meters (typically 2-3m) surrounding each scar in comparison to paired reference quadrats indicating a "halo" effect of each scar. I did not detect a difference in epifaunal community composition or density per blade between mooring and reference sites; however, the relatively constant per blade concentration of epifauna combined with the differences in seagrass biomass between the mooring versus reference sites indicate an overall increase in the total amount of epifauna in areas with less disturbance. Epifaunal community composition was different and between locations and sampling dates indicating these factors are more important than proximity to mooring scarring in determining epifaunal abundance and richness."</p>
FIGURE 5 in A new species of Aphantolana Moore & Brusca, 2003 (Crustacea: Isopoda Cirolanidae) from the Andaman Islands, northern Indian Ocean
FIGURE 5. Aphantolana wandoor sp. nov., holotype ♂ (2.4 mm, PUMB 3531). A, pleopod 1; B, pleopod 2; C, pleopod 3; D, pleopod 4; E, pleopod 5.
FIGURE 4 in A new species of Aphantolana Moore & Brusca, 2003 (Crustacea: Isopoda Cirolanidae) from the Andaman Islands, northern Indian Ocean
FIGURE 4. Aphantolana wandoor sp. nov., holotype ♂ (2.4 mm, PUMB 3531). A, pereopod 1; B, pereopod 2; C, pereopod 4; D, pereopod 7.
FIGURE 3 in A new species of Aphantolana Moore & Brusca, 2003 (Crustacea: Isopoda Cirolanidae) from the Andaman Islands, northern Indian Ocean
FIGURE 3. Aphantolana wandoor sp. nov., holotype ♂ (2.4 mm, PUMB 3531). A, pleonites 1–5; B, maxilla; C, maxillule; D, mandible; E, maxilliped.
FIGURE 2 in A new species of Aphantolana Moore & Brusca, 2003 (Crustacea: Isopoda Cirolanidae) from the Andaman Islands, northern Indian Ocean
FIGURE 2. Aphantolana wandoor sp. nov., holotype ♂ (2.4 mm, PUMB 3531). A, dorsal view; B, coxal plates 1–7; C, anten- nula; D, antenna; E, frontal lamina; F, penes; G, pleotelson; H, uropods.
FIGURES 8–14 in A new species and four new records of Diduga Moore (Lepidoptera, Erebidae Arctiinae) from Thailand
FIGURES 8–14. Male genitalia of Diduga from Thailand (Coll. of OPU and CKC). 8a. D. sphaeracephalus n. sp., holotype (OPU˗037(INU˗10280T). 8b. Apical dentated plate of aedeagus vesica, holotype (OPU˗037(INU˗10280T)). 9. D. albicosta (INU(CKC)˗10369T). 10. D. trichophora (INU(CKC)˗10365T). 11. D. alternota (INU(CKC)˗10374T). 12. D. bispinosa (OPU˗027(INU˗10282T)). 13. D. dubatolovi (OPU˗029(INU˗10278T)). 14. D. allodubatolovi (OPU˗038(INU˗10275T)).
FIGURES 15–17 in A new species and four new records of Diduga Moore (Lepidoptera, Erebidae Arctiinae) from Thailand
FIGURES 15–17. Female genitalia of Diduga from Thailand (Coll. of OPU and CKC). 15. D. sphaeracephalus n. sp., paratype (OPU˗028(INU˗10281T)). 16. D. albicosta (OPU˗036(INU˗10273T)). 17. D. trichophora (INU(CKC)˗10371T).
FIGURES 1–7 in A new species and four new records of Diduga Moore (Lepidoptera, Erebidae Arctiinae) from Thailand
FIGURES 1–7. Adults of Diduga from Thailand (Coll. of OPU and CKC). 1a. D. sphaeracephalus n. sp., male (holotype, OPU˗037(INU˗10280T)). 1b. ditto, female (paratype, OPU˗028(INU˗10281T)). 2a. D. albicosta, male (INU(CKC)˗10369T). 2b. ditto, female (OPU˗036(INU˗10273T)). 3a. D. trichophora, male (INU(CKC)˗10372T). 3b. ditto, female (INU(CKC)˗10366T). 4. D. alternota, male (INU(CKC)˗10374T). 5. D. bispinosa, male (OPU˗037(INU˗10282T)). 6. D. dubatolovi, male (OPU˗029(INU˗10278T)). 7. D. allodubatolovi, male (OPU˗038(INU˗10275T)).
Data from: Persistent near real-time passive acoustic monitoring for baleen whales from a moored buoy: system description and evaluation
1. Managing interactions between human activities and marine mammals often relies on an understanding of the real-time distribution or occurrence of animals. Visual surveys typically cannot provide persistent monitoring because of expense and weather limitations, and while passive acoustic recorders can monitor continuously, the data they collect are often not accessible until the recorder is recovered. 2. We have developed a moored passive acoustic monitoring system that provides near real-time occurrence estimates for humpback, sei, fin, and North Atlantic right whales from a single site for a year, and makes those occurrence estimates available via a publicly accessible website, email and text messages, a smartphone/tablet app, and the U.S. Coast Guard's maritime domain awareness software. We evaluated this system using a buoy deployed off the coast of Massachusetts during 2015-2016 and redeployed again during 2016-2017. Near real-time estimates of whale occurrence were compared to simultaneously collected archived audio as well as whale sightings collected near the buoy by aerial surveys. 3. False detection rates for right, humpback, and sei whales were 0% and nearly 0% for fin whales, while missed detection rates at daily time scales were modest (12-42%). Missed detections were significantly associated with low calling rates for all species. We observed strong associations between right whale visual sightings and near real-time acoustic detections over a monitoring range of 30-40 km and temporal scales of 24-48 hours, suggesting that silent animals were not especially problematic for estimating occurrence of right whales in the study area. There was no association between acoustic detections and visual sightings of humpback whales. 4. The moored buoy has been used to reduce the risk of ship strikes for right whales in a U.S. Coast Guard gunnery range, and can be applied to other mitigation applications.
FIGURES 6–10. Nishada flabrifera Moore. 6 in A new species of genus Nishada Moore, 1878 (Lepidoptera, Erebidae, Arctiinae) from India
FIGURES 6–10. Nishada flabrifera Moore. 6, Adult male, 7, Forewing. 8, Hindwing. 9, Male genitalia. 10, Phallus.
FIGURES 1–5. Nishada pseudochilomorpha Joshi & Singh. 1, Adult male. 2, Forewing. 3, Hindwing. 4, Male genitalia. 5 in A new species of genus Nishada Moore, 1878 (Lepidoptera, Erebidae, Arctiinae) from India
FIGURES 1–5. Nishada pseudochilomorpha Joshi & Singh. 1, Adult male. 2, Forewing. 3, Hindwing. 4, Male genitalia. 5, Phallus.
FIGURE 2. Seba chiltoni Moore, 1987 in Four species of the genus Seba from Japan, with descriptions of two new species (Crustacea: Amphipoda: Sebidae)
FIGURE 2. Seba chiltoni Moore, 1987. Male "1", 3.1 mm (OMNH-Ar-7701). A, left antenna 1, medial view; B, left antenna 2, lateral view; C, labrum and left mandible, anteromedial view; D, right mandible, medial view; E, labium, ventral view; F, right maxilla 1, dorsal view; F1, inner plate of right maxilla 1, dorsal view; F2, apical part of palp of right maxilla 1, dorsal view; F3, apical part of outer plate of right maxilla 1, dorsal view; G, left maxilla 2, ventral view; H, left maxilliped, dorsal view. Scales: 0.05 mm.
FIGURE 1. Seba chiltoni Moore, 1987 in Four species of the genus Seba from Japan, with descriptions of two new species (Crustacea: Amphipoda: Sebidae)
FIGURE 1. Seba chiltoni Moore, 1987. Male "1", 3.1 mm (OMNH-Ar-7701), habitus, left lateral view. Scale: 0.5 mm.
FIGURE 4. Seba chiltoni Moore, 1987. A–D in Four species of the genus Seba from Japan, with descriptions of two new species (Crustacea: Amphipoda: Sebidae)
FIGURE 4. Seba chiltoni Moore, 1987. A–D, male "1", 3.1 mm (OMNH-Ar-7701); E–J, E1, F1, female "1", 3.7 mm (OMNH-Ar-7703); K, male "2", 2.3 mm (OMNH-Ar-7702). A, B, left uropods 1, 2, dorsolateral views; C, left uropod 3, dorsomedial view; D, telson, dorsal view; E, left gnathopod 1, lateral view; E1, palm of left gnathopod 1, lateral view; F, left gnathopod 2, lateral view; F1, apical part of propodus of left gnathopod 2, lateral view, setae omitted; G, left pereopod 7, lateral view; H–J, left pleopods 1–3, posterior views; K, propodus and dactylus of left gnathopod 1, lateral view. Scales: 0.05 mm.
FIGURE 3. Seba chiltoni Moore, 1987 in Four species of the genus Seba from Japan, with descriptions of two new species (Crustacea: Amphipoda: Sebidae)
FIGURE 3. Seba chiltoni Moore, 1987. Male "1", 3.1 mm (OMNH-Ar-7701). A, left gnathopod 1, lateral view; A1, palm of left gnathopod 1, lateral view; B, left gnathopod 2, lateral view; B1, apical part of propodus of left gnathopod 2, lateral view, setae omitted; C–G, left pereopods 3–7, lateral views; H, right epimeral plates 1–3, lateral view. Scales: 0.05 mm.
FIGURE 8. Hippomedon rodericki P.G. Moore, 1989 in The genus Hippomedon in Australian waters (Crustacea, Amphipoda, Lysianassidae, Tryphosinae)
FIGURE 8. Hippomedon rodericki P.G. Moore, 1989, male, 13.5 mm, AM P.69718, from Botany Bay, New South Wales.
FIGURE 10. Hippomedon rodericki P.G. Moore, 1989 in The genus Hippomedon in Australian waters (Crustacea, Amphipoda, Lysianassidae, Tryphosinae)
FIGURE 10. Hippomedon rodericki P.G. Moore, 1989, ovigerous female, 15.2 mm, AM P.69717, from Botany Bay, New South Wales. Scale bars: 0.5 mm.
FIGURE 9. Hippomedon rodericki P.G. Moore, 1989 in The genus Hippomedon in Australian waters (Crustacea, Amphipoda, Lysianassidae, Tryphosinae)
FIGURE 9. Hippomedon rodericki P.G. Moore, 1989, ovigerous female, 15.2 mm, AM P.69717; male, 13.5 mm, AM P.69718, both from Botany Bay, New South Wales. Scale bars: 0.2 mm.
FIGURE 9 in Review of the species of Pelodiaetodes Moore (Coleoptera: Carabidae: Bembidiini: Anillina) of New Zealand
FIGURE 9. SEM illustrations of ovipositor sclerites of Pelodiaetodes species. A–B right ovipositor sclerite, lateral aspect; C– D right gonocoxite 2, ventral aspect. A, D P. prominens; B, E P. moorei; C, F P. nunni. Legend: mbr–medial basal ridge of gonocoxite 2, bla–blade of gonocoxite 2, les–lateral ensiform seta; gc1–gonocoxite 1; gc2–gonocoxite 2; lt–laterotergite; mes– medial ensiform seta; ns–nematiform seta. Scale bars: A–C = 0.05mm; D–F = 0.02mm.
FIGURE 2 in Review of the species of Pelodiaetodes Moore (Coleoptera: Carabidae: Bembidiini: Anillina) of New Zealand
FIGURE 2. SEM illustrations of structural features of Pelodiaetodes species. Basal part of left elytron, dorsal aspect: A P. prominens; B P. nunni. Elytra, dorsal aspect: C P. prominens, D P. nunni. Legend: axt–auxillar tubercle; bm–basal margin; ed2–scutellar seta; ed3–ed6–discal elytral setae; ed8–apical elytral seta; eo1–9–setae 1–9 from the umbilicate series; eg–elytral groove; lb–lateral pronotal bead; sct–scutellum. Scale bars = 0.2mm.
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.