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862 results for “marine fish”

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zenodo28/100

Supplementary material 9 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S6

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 3 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Table S2

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 11 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S8

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 15 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S12

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 7 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S4

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 10 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S7

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 12 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S9

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 2 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Table S1

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 6 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S3

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 13 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S10

opencc-zeroJan 2021View details →
zenodo28/100

Figure 3 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Figure 3 Percentages of the Sint Eustatius marine fish fauna represented by groups of species with different global geographical ranges. GC = Greater Caribbean endemics; NWA = GC plus temperate eastern USA; WA = GC plus Brazil; TA = WA plus central or East Atlantic; and A&P = species found in both the Atlantic and various parts of the Indo-Pacific.

opencc-by-4.0Jan 2021View details →
zenodo28/100

Supplementary material 1 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Figure S1

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 14 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Plate S11

opencc-zeroJan 2021View details →
zenodo28/100

Figure 2 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Figure 2 Study sites at Sint Eustatius Island. Location of dive sites during 2017 and 2020: Black stars indicate submersible dives, blue stars 2017 SCUBA dives, red stars 2020 SCUBA dives (some individual stars indicate multiple dives in very close proximity), purple star an intertidal snorkeling site, and the red outline shows limits of the shore-diving area in 2020. See Suppl. material 2: Table S1 for georeferenced date on dive sites. Generalized 20 m, 30 m, 200 m and 500 m isobaths in blue; other lines indicate marine and terrestrial reserve areas. (Base map from Statiaparks, openstreemap.org, CC-BY-SA 2.0 with bathymetry data corrected from CARMABI/WWF/E.Imms (https://www.dcbd.nl/document/bathymetry-map-seas-surrounding-st-eustatius-saba-and-st-maarten, accessed 10 July 2020)

opencc-by-4.0Jan 2021View details →
zenodo28/100

Figure 1 from: Robertson DR, Estapé CJ, Estapé AM, Peña E, Tornabene L, Baldwin CC (2020) The marine fishes of St Eustatius Island, northeastern Caribbean: an annotated, photographic catalog. ZooKeys 1007: 145-180. https://doi.org/10.3897/zookeys.1007.58515

Figure 1 Location of Sint Eustatius. The Caribbean Sea, with the location of Sint Eustatius island indicated in the inset. Source: Hoetjes and Carpenter (2010: fig. 1).

opencc-by-4.0Jan 2021View details →
dryad28/100

Data from: Spatial and temporal patterns of nest distribution influences sexual selection in a marine fish

In many species, the natural distribution of material resources important for reproduction can profoundly impact reproductive success among individuals and, hence, the opportunity and intensity of sexual selection. Here, we report on a field-based experiment investigating the effects of nest aggregation on sexual selection in a fish, the sand goby (Pomatoschistus minutus). We found that the distribution of potential nests (sparse versus aggregated nest treatments) affected patterns of nest colonization and reproductive success. Specifically, in the treatment with aggregated nesting resources, a greater proportion of nests remained unoccupied by sand goby males. Although the size of nesting males did not differ between treatments, eggs accumulated more rapidly when nests were sparsely distributed. We found that the opportunity for selection decreased over time with the accumulation of eggs in the nests in both the aggregated and sparse treatments. Moreover, the effect of male size on reproductive success was influenced by an interaction between nest distribution and time, with the selection gradient being highest right after nest colonization when nests were aggregated, while the opposite pattern was observed in the sparse nest treatment. Such findings highlight the vital role that environmental and social factors can play in determining the importance of male phenotypic traits (in this case, male size). More broadly, our results also underscore how the natural distribution of resources, both in space and time, can impact the strength of sexual selection acting on wild animal populations.

opencc-zeroDec 2017View details →
dryad28/100

Data from: Effects of warming rate, acclimation temperature and ontogeny on the critical thermal maximum of temperate marine fish larvae

Most of the thermal tolerance studies on fish have been performed on juveniles and adults, whereas limited information is available for larvae, a stage which may have a particularly narrow range in tolerable temperatures. Moreover, previous studies on thermal limits for marine and freshwater fish larvae (53 studies reviewed here) applied a wide range of methodologies (e.g. the static or dynamic method, different exposure times), making it challenging to compare across taxa. We measured the Critical Thermal Maximum (CTmax) of Atlantic herring (Clupea harengus) and European seabass (Dicentrarchus labrax) larvae using the dynamic method (ramping assay) and assessed the effect of warming rate (0.5 to 9°C h-1) and acclimation temperature. The larvae of herring had a lower CTmax (lowest and highest values among 222 individual larvae, 13.1 – 27.0 °C) than seabass (lowest and highest values among 90 individual larvae, 24.2 – 34.3 °C). At faster rates of warming, larval CTmax significantly increased in herring, whereas no effect was observed in seabass. Higher acclimation temperatures led to higher CTmax in herring larvae (2.7 ± 0.9°C increase) with increases more pronounced at lower warming rates. Pre-trials testing the effects of warming rate are recommended. Our results for these two temperate marine fishes suggest using a warming rate of 3 - 6 °C h-1: CTmax is highest in trials of relatively short duration, as has been suggested for larger fish. Additionally, time-dependent thermal tolerance was observed in herring larvae, where a difference of up to 8°C was observed in the upper thermal limit between a 0.5- or 24-h exposure to temperatures >18°C. The present study constitutes a first step towards a standard protocol for measuring thermal tolerance in larval fish.

opencc-zeroDec 2016View details →
dryad28/100

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.

opencc-zeroDec 2016View details →
dryad28/100

Data from: Daytime eyeshine contributes to pupil camouflage in a cryptobenthic marine fish

Ocular reflectors enhance eye sensitivity in dim light, but can produce reflected eyeshine when illuminated. Some fish can occlude their reflectors during the day. The opposite is observed in cryptic sit-and-wait predators such as scorpionfish and toadfish, where reflectors are occluded at night and exposed during the day. This results in daytime eyeshine, proposed to enhance pupil camouflage by reducing the contrast between the otherwise dark pupil and the surrounding tissue. In this study, we test this hypothesis in the scorpionfish Scorpaena porcus and show that eyeshine is the result of two mechanisms: the previously described Stratum Argenteum Reflected (SAR) eyeshine, and Pigment Epithelium Transmitted (PET) eyeshine, a newly described mechanism for this species. We confirm that the ocular reflector is exposed only when the eye is light-adapted, and present field measurements to show that eyeshine reduces pupil contrast against the iris. We then estimate the relative contribution of SAR and PET eyeshine to pupil brightness. Visual models for different light scenarios in the field show that daytime eyeshine enhances pupil camouflage from the perspective of a prey fish. We propose that the reversed occlusion mechanism of some cryptobenthic predators has evolved as a compromise between camouflage and vision.

opencc-zeroDec 2017View details →
dryad28/100

Data from: Why pair? Evidence of aggregative mating in a socially monogamous marine fish (Siganus doliatus, Siganidae)

Many species live in stable pairs, usually to breed and raise offspring together, but this cannot be assumed. Establishing whether pairing is based on mating, or an alternative cooperative advantage, can be difficult, especially where species show no obvious sexual dimorphism and where the act of reproduction itself is difficult to observe. In the tropical marine fishes known as rabbitfish (Siganidae), half of extant species live in socially monogamous, territorial pairs. It has been assumed that partnerships are for mating, but the reproductive mode of pairing rabbitfish is currently unconfirmed. Using passive acoustic telemetry to track movements of fishes belonging to one such species (Siganus doliatus), we provide the first evidence that paired adult fish undertake highly synchronized migrations with multiple conspecifics on a monthly cycle. All tagged individuals migrated along the same route in three consecutive months and were absent from home territories for 2–3 days just after the new moon. The timing and directionality of migrations suggest that S. doliatus may form spawning aggregations, offering the potential for exposure to multiple reproductive partners. The finding raises fundamental questions about the basis of pairing, mate choice and partnership longevity in this family.

opencc-zeroDec 2014View details →

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Allen Brain Atlas

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neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record