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443 results for “Eastern Tropical Pacific”
Fig. 5 in The polyclads (Platyhelminthes: Polycladida) from the Tropical Eastern Pacific: Commented checklist and description of a new species
Fig. 5. State of knowledge of the polyclads described and recorded in the Tropical Eastern Pacific; species accumulation curve by decade.
Fig. 4 in The polyclads (Platyhelminthes: Polycladida) from the Tropical Eastern Pacific: Commented checklist and description of a new species
Fig. 4. State of knowledge of the polyclads and frequency of described and recorded species by decade in the Tropical Eastern Pacific.
Fig. 1 in The polyclads (Platyhelminthes: Polycladida) from the Tropical Eastern Pacific: Commented checklist and description of a new species
Fig. 1. Callioplana marianae sp. nov., paratype, ⚥ (UMAR PLAT–047). A. Specimen in vivo. B. Specimen preserved in ethanol. C–D. Specimen stained in Mayer's carmalum and cleared in methyl salicylate. E–I. Details of C, in whole mount. E–F, H. Anterior region of the body. E. Brain. F. Nuchal tentacle. G. Pharynx. H. Tentacular and cerebral eyes. I. Male and female reproductive system. Abbreviations: b = brain; ce = cerebral eyes; gcm = globuli cell masses; lv = Lang's vesicle; nt = nuchal tentacle; p = pharynx; pp = penis papilla; pv = prostatic vesicle; sv = seminal vesicle; te = tentacular eyes; u = uterus.
Fig. 6 in The polyclads (Platyhelminthes: Polycladida) from the Tropical Eastern Pacific: Commented checklist and description of a new species
Fig. 6. Historical records of polyclads species distribution in the Tropical Eastern Pacific. The number outside the parentheses indicates the total number of described and recorded species, while the number inside the parentheses indicates those with a type locality in the area.
Linked collectors and determiners for: New records of sabellids and serpulids (Polychaeta: Sabellidae, Serpulidae) from the Tropical Eastern Pacific.
Natural history specimen data linked to collectors and determiners held within, "New records of sabellids and serpulids (Polychaeta: Sabellidae, Serpulidae) from the Tropical Eastern Pacific". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4d1b5b33-2741-4f58-b920-d3c8f6abbbff">https://bionomia.net/dataset/4d1b5b33-2741-4f58-b920-d3c8f6abbbff</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4d1b5b33-2741-4f58-b920-d3c8f6abbbff">https://gbif.org/dataset/4d1b5b33-2741-4f58-b920-d3c8f6abbbff</a>. Formatted as a Frictionless Data package.
Table 1 in The polyclads (Platyhelminthes: Polycladida) from the Tropical Eastern Pacific: Commented checklist and description of a new species
<p><b>Table 1.</b> Comparison of the morphological characters of <i>Callioplana marianae</i> sp. nov. with other two species of the genus.</p><table><tbody><tr><th><b>Taxa</b></th><th><i>Callioplana marginata</i></th><th><i>Callioplana evelinae</i></th><th><i>Callioplana marianae</i> sp. nov.</th></tr></tbody><tbody><tr><th><b>References</b></th><td>Stimpson 1857: 4, 11; Yeri & Kaburaki 1918: 31–34, pl. 1 fig. 1, text figs 35–37</td><td>Marcus 1954: 476–479, 485, figs 71–76</td><td>This study</td></tr><tr><th><b>Type locality</b></th><td>? Oshima Island, Japan</td><td>San Sebastian Island, Brazil</td><td>Camarón Beach, Oaxaca, Mexico</td></tr><tr><th><b>Distribution</b></th><td>Referred by Stimpson as Ousima Island, Sunosaki and Osaka, Japan</td><td>San Sebastian Island, Brazil</td><td>Only known from Oaxaca, Mexico</td></tr><tr><th></th><td></td><td>Intertidal, breakwater zone; between woods, coarse sand and rocks;</td><td></td></tr><tr><th><b>Habitat</b></th><td>Under rocks; depth 1.25 m</td><td>sharing habitat with algae of the genus <i>Padina</i>, polychaetes as <i>Polygordius</i> and cephalochordates</td><td>Intertidal, breakwater zone; under rocks</td></tr><tr><th><b>Body (Long</b> × <b>wide mm)</b></th><td>Oval (50–30 × 15–7)</td><td>Oval (10 × 4)</td><td>Elliptical (15–20 × 10–12) (Figs 1A–D, 3A)</td></tr><tr><th></th><td></td><td>Color ivory, with small brownish spots condensed into three fine</td><td></td></tr><tr><th><b>Dorsal coloration and colour pattern</b></th><td>Black-brown with a reddish-orange margin (Stimpson 1857); velvety black, reddish-brown margin (Yeri & Kaburaki 1918)</td><td>longitudinal grooves; transverse red stripes (juveniles) or black (adults) in front of tentacles; black spots on the anterior margin giving the appearance of marginal eyes</td><td>Beige background coloration, with light brown and white pigmentation that produce a reticulated appearance (Fig. 1A–B)</td></tr><tr><th><b>Nuchal tentacles</b></th><td>Conical, orange in the apical region (Yeri & Kaburaki 1918)</td><td>Pointed, brown colored in the apical region</td><td>Rudimentary nipple-shaped (Figs 1F, 3B)</td></tr><tr><th><b>Prostatic vesicle morphology and position</b></th><td>Oval, located anterior and dorsal to the seminal vesicle (Yeri & Kaburaki 1918)</td><td>Oval, located ventral to the seminal vesicle</td><td>Oval, anterior to the seminal vesicle (Figs 1I, 2D, 3C–D)</td></tr><tr><th><b>Penis papilla</b></th><td>Elongated and slender cylindrical, covered by a sheath (Yeri & Kaburaki 1918)</td><td>Elongate</td><td>Short (Fig. 2F)</td></tr><tr><th><b>Stylet</b></th><td>Absent</td><td>Absent</td><td>Present (Figs 2B, G, 3C–D)</td></tr><tr><th><b>Lang’s vesicle</b></th><td>Double or bifurcated, anterior to the male gonopore</td><td>Double or bifurcated, anterior to the male gonopore</td><td>Tripartite, posterior to the male gonopore (Figs 1I, 2A, 3C–D)</td></tr></tbody></table>
FIG. 3 in New record and description of the male gonopods of Paeduma cylindraceum (Bell, 1859) from the tropical eastern Pacific (Decapoda, Brachyura, Hexapodidae)
FIG. 3. — First gonopod of species of Hexapodidae Miers, 1886: A, Hexapinus buchanani (Monod, 1956); B, Hexapinus granuliferus (Campbel & Stephenson, 1970); C, Hexapus anfractus (Rathbun, 1909);D, Hexapus estuarinus Sankarankutty,1975; E, Hexapus sexpes (Fabricius, 1798); F, G, Hexalaughlia orientalis (Rathbun, 1909); H, Parahexapus africanus Balss, 1922; I, Pseudohexapus platydactylus Monod, 1956; J, Spiroplax spiralis (Barnard, 1950); K, Thaumastoplax anomalipes Miers, 1881; L, Trioplax stebbingi (Barnard, 1947); M, Tritoplax stephenseni (Serène & Soh, 1976); N, Latohexapus granosus Huang, Hsueh & Ng, 2002. A-C, G-L, from Manning & Holthuis (1981); D, from Sankarankutty (1975); E, F, M, from Serène & Soh (1976); N, from Huang et al. (2002).
FIG. 1 in New record and description of the male gonopods of Paeduma cylindraceum (Bell, 1859) from the tropical eastern Pacific (Decapoda, Brachyura, Hexapodidae)
FIG. 1. — Paeduma cylindraceum (Bell, 1859), male (EMU-8270), CW 13.7 mm: A, dorsal view; B, ventral view; C, right first gonopod, ventral view; D, right second gonopod, ventral view, and dorsal view of tip. Scale bars: C, 1 mm; D, 0.5 mm.
FIG. 3. — Stratiotes mclaughlinae n in A new species of Stratiotes Thomson, 1899 (Anomura, Paguroidea, Diogenidae) from the eastern tropical Pacific
FIG. 3. — Stratiotes mclaughlinae n. sp.: A-C, ♂ holotype (EMU-752); D-G, ♀ paratype (EMU-5671); A, sternite XII (third pereopods); B, first pleopod, internolateral view; C, second pleopod, internal view; D, second pleopod, external view; E, third pleopod, external view; F, fourth pleopod, external view; G, fifth pleopod, external view. Scale bars: 0.5 mm.
FIG. 1. — Stratiotes mclaughlinae n in A new species of Stratiotes Thomson, 1899 (Anomura, Paguroidea, Diogenidae) from the eastern tropical Pacific
FIG. 1. — Stratiotes mclaughlinae n. sp., ♂ holotype (EMU-752): A, shield and cephalic appendages, dorsal view; B, right cheliped, dorsal view (setae omitted); C, right dactyl and palm, lateral view; D, right second pereopod, inner and outer views; E, left third pereopod, inner view; F, right fourth pereopod, lateral view; G, dactyl of right fourth pereopod, lateral view; H, telson, dorsal view. Scale bars: A-F, 1 mm; G, H, 0.5 mm.
FIG. 2. — Stratiotes mclaughlinae n in A new species of Stratiotes Thomson, 1899 (Anomura, Paguroidea, Diogenidae) from the eastern tropical Pacific
FIG. 2. — Stratiotes mclaughlinae n. sp., mouthparts: A, ♀ paratype (EMU-6712); B-D, ♂ holotype (EMU-752): A, right maxillule and magnification of the endopod, internal view; B, right maxilla, internal view; C, right first maxilliped, internal view; D, right second maxilliped, internal view; E, right third maxilliped, internal view. Scale bars: 0.5 mm.
OISSTv2 standardized daily SST in Eastern tropical Pacific
<p>OISSTv2 standardized daily sea surface temperatures (SST) of 11 different 60x60 latitutde x longitude tiles in the eastern tropical Pacific.</p> <p>Time coverage: 1982-2021</p>
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 from: Genomic, ecological, and morphological approaches to investigating species limits: a case study in modern taxonomy from Tropical Eastern Pacific surgeonfishes
A wide variety of species are distinguished by slight color variations. However, molecular analyses have repeatedly demonstrated that coloration does not always correspond to distinct evolutionary histories between closely related groups, suggesting that this trait is labile and can be misleading for species identification. In the present study, we analyze the evolutionary history of sister species of Prionurus surgeonfishes in the Tropical Eastern Pacific (TEP), which are distinguished by the presence or absence of dark spots on their body. We examined the species limits in this system using comparative specimen-based approaches, a mitochondrial gene (COI), more than 800 nuclear loci (Ultraconserved Elements), and abiotic niche comparisons. The results indicate there is a complete overlap of meristic counts and morphometric measurements between the two species. Further, we detected multiple individuals with intermediate spotting patterns suggesting that coloration is not diagnostic. Mitochondrial data recovered a single main haplotype shared between the species and all locations resulting in a complete lack of structure (ST = 0). Genomic analyses also suggest low levels of genetic differentiation (FST = 0.013), and no alternatively fixed SNPs were detected between the two phenotypes. Furthermore, niche comparisons could not reject niche equivalency or similarity between the species. These results suggest that these two phenotypes are conspecific and widely distributed in the TEP. Here we recognize Prionurus punctatus Gill 1862 as a junior subjective synonym of P. laticlavius (Valenciennes 1846). The underlying causes of phenotypic variation in this species is unknown. However, this system gives insight into general evolutionary dynamics within the TEP.
FIGURE 5 in New records of sabellids and serpulids (Polychaeta: Sabellidae, Serpulidae) from the Tropical Eastern Pacific
FIGURE 5. Distribution of Hydroides glandifera, H. humilis, H. inermis and H. ochotereana
FIGURE 6 in New records of sabellids and serpulids (Polychaeta: Sabellidae, Serpulidae) from the Tropical Eastern Pacific
FIGURE 6. Distribution of Hydroides panamensis, H. sanctaecrucis, H. similis and H. trompi.
FIGURE 4 in New records of sabellids and serpulids (Polychaeta: Sabellidae, Serpulidae) from the Tropical Eastern Pacific
FIGURE 4. Distribution of Hydroides deleoni, H. dirampha, H. elegans and H. gairacensis..
Whale shark tracking data from the eastern tropical Pacific
<p>These two data files contain Argos position data and subsurface time-at-temperature data from whale sharks tagged at Darwin's Arch, Galapagos during 2011 - 2012.</p>
FIG. 1 in Revision of the genus Actinostella (Cnidaria: Actiniaria: Actinioidea) from tropical and subtropical western Atlantic and eastern Pacific: redescriptions and synonymies
FIG. 1. Geographic distribution of species of Actinostella.
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