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101 results for “, Marine reserve”
Data from: Isolation and no-entry marine reserves mitigate anthropogenic impacts on grey reef shark behavior
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Data from: Effects of Poor Knights Islands Marine Reserve on demersal fish populations
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Data from: Dispersal of a near-shore marine fish connects marine reserves and adjacent fished areas along an open coast
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Data from: Variation in responses of fishes across multiple reserves within a network of marine protected areas in temperate waters
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Data from: Mapping habitats in a marine reserve showed how a 30-year trophic cascade altered ecosystem structure
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Data from: The role of marine reserves in the replenishment of a locally-impacted population of anemonefish on the Great Barrier Reef
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Data from: Potential of a no-take marine reserve to protect home ranges of anadromous brown trout (Salmo trutta)
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Data from: Selection on fish personality differs between a no-take marine reserve and fished areas
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Figure 8 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 8. Gyrineum natator. Phase-contrast micrographs of the salivary glands of three individuals following treatment with barium chloride for 50 minutes. (A–C) Three untreated controls; (D–F) three treated individuals.
Figure 2 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 2. Gyrineum natator. The holes made in four shells (A–D) of Saccostrea mordax by individuals held in experimental aquaria. Only A shows a near-circular access hole, but other irregular ones (B–D) appear to have been created by acid attack as there would be no need for the radula alone to make such large holes.
Figure 4 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 4. Gyrineum natator. The relationship between shell height (in mm) and wet tissue weights [Log(W + 1) (in grams)] of seven individuals including the two experimental animals with shell heights of 34.6 and 33.6 mm.
Figure 5 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 5. Gyrineum natator. The accumulated % wet tissue weights of oyster tissues consumed by the two approximately equal-sized individuals of G. natator held in filtered and unfiltered seawater aquaria.
Figure 1 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 1. Gyrineum natator. The living animal as seen from the ventral aspect crawling on an upturned sheet of glass immersed in seawater, and showing the extended proboscis.
Figure 7 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 7. Gyrineum natator. (A) A transverse section through one of the paired salivary glands and the associated pharyngeal (oesophageal) gland; (B) developing salivary gland tubules at the outer edge of the salivary gland; (C) fully developed sulphuric acid producing salivary gland cells; (D) a transverse section through a pharyngeal (oesophageal) gland tubule; (E) a transverse section through the salivary gland/pharyngeal gland duct.
Figure 3 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 3. Saccostrea mordax. The relationship between total weight [Log(TotW + 1) (in grams)] and wet tissue weights [Log(W + 1) (in grams)] of the 34 oyster individuals.
Figure 9 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 9. Gyrineum natator. Phase-contrast micrographs of (A) the salivary gland and (B) the pharyngeal (oesophageal) gland after treatment with barium chloride for 50 minutes.
Figure 6 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 6. Gyrineum natator. The foregut anatomy, as seen from the dorsal aspect, and showing the hypertrophied and paired salivary glands and the single pharyngeal (oesophageal) gland. Redrawn after Taylor (1998).
Data recreational fishing yields Cerbère-Banyuls marine reserve
<p>Catch per unit effort (CPUE, in n/line/hour) and weight by unit effort (WPUE, in g/line/hour) of onshore and offshore recreational fishermen fishing inside and outside of the Cerbère-Banyuls natural marine reserve in 2005-2014.</p>
Data from: Evolution of movement rate increases the effectiveness of marine reserves for the conservation of pelagic fishes
Current debates about the efficacy of no-take marine reserves (MR) in protecting large pelagic fish such as tuna and sharks have usually not considered the evolutionary dimension of this issue, which emerges because the propensity to swim away from a given place, like any other biological trait, will probably vary in a heritable fashion among individuals. Here, based on spatially-explicit simulations, we investigated whether selection to remain in MRs to avoid higher fishing mortality can lead to the evolution of more philopatric fish. Our simulations, which covered a range of life histories among tuna species (skipjack tuna vs. Atlantic Bluefin tuna) and shark species (great white sharks vs. spiny dogfish) suggested that MRs were most effective at maintaining viable population sizes when movement distances were lowest. Decreased movement rate evolved following the establishment of marine reserves, and this evolution occurred more rapidly with higher fishing pressure. Evolutionary reductions in movement rate led to increases in within-reserve population sizes over the course of the 50 years following MR establishment, although this varied among life-histories, with skipjack responding fastest and great white sharks slowest. Our results suggest the evolution of decreased movement can augment the efficacy of marine reserves, especially for species, such as skipjack tuna, with relatively short generation times. Even when movement rates did not evolve substantially over 50 years (e.g., given long generation times or little heritable variation), marine reserves were an effective tool for the conservation of fish populations when mean movement rates were low or MRs were large.
Fig. 2 in Ichthyoplankton of Arvoredo Biological Marine Reserve, Santa Catarina, Brazil
Fig. 2. Average densities of (a) eggs and (b) larvae collected during the winter and summer periods to six stations in the Arvoredo Biology Marine Reserve (Brazil) in different campaign (1- 1997/1998, 2- 2007/2008, and 3- 2008/2009). The vertical bar represents the confidence interval.
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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.