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273 results for “Eastern Pacific Ocean”
Suppl. figures of otoliths of pelagic shorefish larvae captured over the Galapagos Rift for Victor, B.C. (2023) Rapid long-distance multispecies transport of shorefish larvae to the oceanic tropical eastern Pacific, revealed by DNA-barcodes and otolith aging of larvae captured over the Galapagos Rift
<p>Supplementary figures of otoliths of pelagic shorefish larvae captured over the Galapagos Rift</p> <p>Victor, B.C. (2023)</p> <p><strong>Rapid long-distance multispecies transport of shorefish larvae to the oceanic tropical eastern Pacific, revealed by DNA-barcodes and otolith aging of larvae captured over the Galapagos Rift</strong></p> <p>in volume: Early Life History and Biology of Marine Fishes: Research inspired by the work of H Geoffrey Moser</p> <p>Figure Sup A1 Sagittal otolith of 5.9 mm SL Stegastes sp. fish larva (Pomacentridae) captured over the Galapagos Rift, age since hatching is 23 days.</p>
Suppl. figures of pelagic shorefish larvae captured over the Galapagos Rift for Victor, B.C. (2023) Rapid long-distance multispecies transport of shorefish larvae to the oceanic tropical eastern Pacific, revealed by DNA-barcodes and otolith aging of larvae captured over the Galapagos Rift
<p>Supplementary figures of pelagic shorefish larvae captured over the Galapagos Rift</p> <p>Victor, B.C. (2023)</p> <p><strong>Rapid long-distance multispecies transport of shorefish larvae to the oceanic tropical eastern Pacific, revealed by DNA-barcodes and otolith aging of larvae captured over the Galapagos Rift</strong></p> <p>in volume: Early Life History and Biology of Marine Fishes: Research inspired by the work of H Geoffrey Moser</p> <p>Figure S1 Gobioid fish larvae captured over the Galapagos Rift.</p> <p>Figure S2 Labrid fish larvae captured over the Galapagos Rift.</p> <p>Figure S2. Pomacentrid fish larvae captured over the Galapagos Rift.</p> <p>Figure S4 Lythrypnus sp 5.4 mm SL fish larva captured over the Galapagos Rift.</p> <p>Figure S4a Lythrypnus sp 5.4 mm SL fish larva (head) captured over the Galapagos Rift.</p> <p>Figure S5 Abudefduf troschelii 7.3 mm SL fish larva captured over the Galapagos Rift.</p> <p>Figure S6 Chaetodon humeralis 8.9 mm SL fish larva captured over the Galapagos Rift.</p> <p>Figure S7 Gerreidae 10.6 mm SL fish larva captured over the Galapagos Rift.</p> <p>Figure S8 Neoniphon suborbitalis 6.8 mm SL fish larva captured over the Galapagos Rift.</p> <p>Figure S9 Ophioblennius steindachneri 10.6 mm SL fish larva captured over the Galapagos Rift.</p> <p>Figure S9a Ophioblennius steindachneri 10.6 mm SL fish larva (head) captured over the Galapagos Rift.</p> <p>Figure S9b Ophioblennius steindachneri 10.6 mm SL fish larva (ventral) captured over the Galapagos Rift.</p> <p>Figure Sup10 Sphoeroides lobatus 12.0 mm SL fish larva captured over the Galapagos Rift.</p>
Data and code from: You shall not pass, the Pacific oxygen minimum zone creates a boundary to shortfin mako shark distribution in the Eastern North Pacific Ocean
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Large-scale patterns of green turtle trophic ecology in the eastern Pacific Ocean
<p><span><span><span><span><span><span><span><span><span><span><span>Trophic position and niche width are fundamental components of a species' ecology, reflecting resource use, and influencing key demographic parameters such as somatic growth, maturation, and survival. The present data file contains results of stable isotope analysis (stable-carbon, δ<sup>13</sup>C; stable-nitrogen, δ<sup>15</sup>N values) that was conducted on bulk skin tissue of 718 green sea turtles (<i>Chelonia mydas</i>) distributed among 16 foraging areas in the eastern Pacific from the US to Chile, a range spanning ~10,000 km. These study sites </span></span></span></span></span></span></span></span></span></span></span>were distributed across a latitudinal range from 33.736 °N to 23.098°S in the Eastern Pacific (Site Code): Long Beach, USA (LB); San Diego Bay, USA (SDB); north Gulf of Ulloa, Mexico (NGU); Magdalena Bay, Mexico (BMA); Los Angeles Bay, Mexico (BLA); Infiernillo Channel, Mexico (CIN); Navachiste Bay, Mexico (NAV); Dulce Gulf, Costa Rica (DUL); Cocos Island, Costa Rica (COC); Gorgona Island, Colombia (GOR); Punta Espinosa, Galapagos Islands, Ecuador (IGP); Bahia Elizabeth, Galapagos Islands, Ecuador (IGE); Caleta Derek, Galapagos Islands, Ecuador (IGD); oceanic waters, Peru (PPE); Pisco Paracas Bay, Peru (PAR); and Mejillones Bay, Chile (MEJ). <span><span><span><span><span><span><span><span><span><span><span>Substantial variability in bulk tissue δ<sup>13</sup>C and δ<sup>15</sup>N values was found within and among sites. These data were also used to calculate the isotope niche space (used as a proxy for ecological niche space) using the Bayesian ellipse approach, and we found that isotope niche space varied among sites, likely influenced by the diversity of prey types and relative input of terrestrial- vs. marine-derived nutrients. In addition to providing additional spatial resolution for δ<sup>13</sup>C and δ<sup>15</sup>N isoscapes in the eastern Pacific, especially in coastal habitats, this study and resultant dataset further establish stable isotope analysis as an effective tool to study the trophic ecology of sea turtles across a variety of food webs and habitats. </span></span></span></span></span></span></span></span></span></span></span></p>
Data from: Connections between the Southern Ocean and the Eastern tropical Pacific in unforced and forced climate model simulations
<p>The sea surface temperature (SST) over the eastern tropical Pacific significantly influences global-mean climate feedback and may be driven in part by the SST over the Southern Ocean. Previous studies demonstrated a teleconnection from the Southern Ocean to the eastern tropical Pacific by perturbing the Southern Ocean climate. We investigate if this teleconnection holds in a fully coupled, freely running climate system using CMIP6 models. We assess the relationship between the Southern Ocean (SO) and the eastern tropical Pacific (SEP) by calculating correlations between SO and SEP SST timeseries within each model and regressions between mean SO and SEP SSTs across models. We show robust, positive SO-SEP relationships in an unforced climate using pre-industrial SSTs, in a forced climate using SST anomalies between pre-industrial and quadrupled CO<sub>2</sub> simulations, and in the SST pattern of the forced response relative to the global-mean SST anomaly. The strength of SO-SEP correlations is positively related to the stratocumulus cloud feedback off the west coast of South America, and negatively related to ocean heat uptake in the same region. As both shortwave cloud feedback and ocean heat uptake are underestimated in climate models, understanding their effects on SO-SEP teleconnections and their interactions is crucial for determining the strength of SO-SEP teleconnection in the real world and its trustworthiness in climate model projection.</p>
Figure 2 in First report of gray whale (Eschrichtius robustus, Lilljeborg, 1861) conjoined twin calves in the Eastern Pacific Ocean
Figure 2. Eschrichtius robustus specimens showing caudal area.
Figure 1 in First report of gray whale (Eschrichtius robustus, Lilljeborg, 1861) conjoined twin calves in the Eastern Pacific Ocean
Figure 1. Front view of Eschrichtius robustus specimens.
Ocean Gateways and Ocean Circulation Dynamics: Unveiling the Deep Water-Mass properties in the Western Equatorial Pacific and Eastern Indian Ocean since the middle
<p>File contains a dataset related to census counts and stable isotopes that we used to write our manuscript.</p>
Large-scale patterns of green turtle trophic ecology in the eastern Pacific Ocean
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Data from: The Relationship between the Southern Ocean and the Eastern tropical Pacific in unforced and forced climate model simulations
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FIGURE 24. Orbiniella tumida n in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 24. Orbiniella tumida n. sp. A, anterior end, dorsal view; B, anterior end, ventral view; C, posterior end, dorsal view; D, parapodium from mid-body setiger, anterior view; E–H, acicular spines. A–B, D–F, holotype (LACM-AHF Poly 11662); C, paratype (CASIZ 234032).
FIGURE 22. Orbiniella longilobata n in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 22. Orbiniella longilobata n. sp. A, anterior end, dorsal view; B, anterior end, ventral view; C, middle body setiger, anterior view; D–E, notopodial spines. A, C–E, holotype (MCZ 153588); B, paratype (MCZ 153590).
FIGURE 20. Orbiniella eugeneruffi n in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 20. Orbiniella eugeneruffi n. sp. Holotype MCZ 153578): A, anterior end, dorsal view; B, anterior end, ventral view; C, posterior end, dorsal view. Paratype (MCZ 153579): D, mid-body setiger, anterior view (inset not to scale).
FIGURES 17. Leodamas bathyalis n in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURES 17. Leodamas bathyalis n. sp. A, anterior end dorsal view; B, thoracic setiger 9, right, posterior view; C, middle abdominal setiger, anterior view; D, neuropodial uncini (holotype); E, neuropodial uncini (paratype); F, furcate setae. A–D, F, holotype (MCZ 153569); E, paratype (MCZ 153700).
FIGURE 13. Naineris uncinata Hartman, 1957 in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 13. Naineris uncinata Hartman, 1957. (MCZ 153572): A, anterior end, dorsal view; B, anterior end, right lateral view; C, posterior thoracic segments, right lateral view; D, posterior thoracic parapodium, anterior view; E, fascicle of thoracic neurosetae; F, detail of thoracic neuropodial uncini and capillaries. Stained with Shirlastain A.
FIGURE 11. Califia calida Hartman, 1957 in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 11. Califia calida Hartman, 1957. (CASIZ 234031): A, anterior end, dorsal view. (CASIZ 234031): B, anterior end, ventral view. (CASIZ 234040): C, setiger 2, anterior view; D, middle abdominal setiger, anterior view; E, long, smooth neuropodial spine from setiger 2; F, short, ribbed neuropodial spine, setiger 2; G, abdominal notopodial furcate seta; H, posterior end, dorsal view.
FIGURE 10. Berkeleyia lelievre n in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 10. Berkeleyia lelievre n. sp. A, anterior end, dorsal view; B, thoracic setiger 7, anterior view; C, posterior abdominal setiger, anterior view, insets, detail of tips of spines, not to scale. A, C, holotype (MCZ 154094), B, paratype (MCZ 154095).
FIGURE 5. Leitoscoloplos lunulus n in New species and records of deep-water Orbiniidae (Annelida, Polychaeta) from the Eastern Pacific continental slope, abyssal Pacific Ocean, and the South China Sea
FIGURE 5. Leitoscoloplos lunulus n. sp. A, anterior end, dorsal view; B, anterior end, ventral view; C, anterior end, right lateral view; D, pygidium, right lateral view; E, thoracic setiger 7, right, posterior view. A–B, D holotype (LACM-AHF Poly 11660); C, E, paratype (CASIZ 234041).
FIGURE 1. A–B in First record of hybridization in Caranx Lacepède, 1801 (Carangidae: Perciformes) in the Tropical Eastern Pacific Ocean
FIGURE 1. A–B. Specimen of C. melampygus x C. sexfasciatus, 576 mm SL (UCR 3209-001), captured at Isla Montuosa, Pacific coast of Panama (7.467472, -82.266556; 30 m depth). (A) Fresh and (B) after preservation. C–D. Preserved specimens, representatives of the parental species: (C) C. melampygus (UCR 0423-027, 153 mm SL) and (D) C. sexfasciatus (UCR 3112- 003, 122 mm SL). Scale bar=50 mm.
FIGURE 2 in First record of hybridization in Caranx Lacepède, 1801 (Carangidae: Perciformes) in the Tropical Eastern Pacific Ocean
FIGURE 2. Consensus tree of selected members of Caranx. Topology inferred combining the information of five different models: Neighbor-Joining (NJ), Bayesian Inference (BI), Maximum-Likelihood (ML), Minimum Evolution (ME) and Maximum Parsimony (MP) for a total of 19 (626-bp) COX1 sequences. Numbers at nodes represent support values in percentage (posterior probability for BI) for each one of the five models, respectively. The tree is rooted with Nematistius pectoralis.
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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.