35 research outputs found
A new deep-sea eelpout of the genus Pyrolycus (Teleostei: Zoarcidae) associated with a hydrothermal seep on the Pacific margin of Costa Rica
A new species of the zoarcid genus Pyrolycus Machida & Hashimoto, 2002, Pyrolycus jaco sp. nov., is described from
a hydrothermal seep environment named JacĂł Scar in the eastern Pacific of Costa Rica. Four specimens were collected
in 2018 between 1746–1795 m among tubeworm colonies around the seep. The new species is differentiated from its
two western Pacific congeners by having a shorter head, snout, jaw, and pectoral fins. It is further diagnosed by having
three postorbital pores and two occipital pores. Molecular sequences of the cytochrome c oxidase I gene are provided and
are the first for the genus. The character states indicating miniaturization in this species are discussed. This is the first
vertebrate species known from this composite reducing ecosystem and is the fourth hydrothermally-associated zoarcid
from the eastern Pacific
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Checklist of marine and estuarine fishes from the Alaska–Yukon Border, Beaufort Sea, to Cabo San Lucas, Mexico
This paper is a checklist of the fishes that have been documented, through both published and unpublished sources, in marine and estuarine waters, and out 200 miles, from the United States-Canadian border on the Beaufort Sea to Cabo San Lucas, Mexico. A minimum of 241 families and 1,644 species are known within this range, including both native and nonnative species. For each of these species, we include maximum size, geographic and depth ranges, whether it is native or nonnative, as well as a brief mention of any taxonomic issues
A new species of western Atlantic lizardfish (Teleostei: Synodontidae: Synodus) and resurrection of Synodus bondi Fowler, 1939, as a valid species from the Caribbean with redescriptions of S. bondi, S. foetens (Linnaeus, 1766), and S. intermedius (Agassiz, 1829)
Western Atlantic synodontid species were studied as part of an ongoing effort to reanalyze Caribbean shorefish diversity. A neighbor-joining tree constructed from cytochrome c oxidase I (COI) data revealed 2 highly divergent genetic lineages within both Synodus intermedius (Agassiz, 1829) (Sand Diver) and S. foetens (Linnaeus, 1766) (Inshore Lizardfish). A new species, Synodus macrostigmus, is described for one of the S. intermedius lineages. Synodus macrostigmus and S. intermedius differ in number of lateral-line scales, caudal pigmentation, size of the scapular blotch, and shape of the anterior-nostril flap. Synodus macrostigmus and S. intermedius have overlapping geographic and depth distributions, but S. macrostigmus generally inhabits deeper water (>28 m) than does S. intermedius and is known only from coastal waters of the southeastern United States and the Gulf of Mexico, in contrast to those areas and the Caribbean for S. intermedius. Synodus bondi Fowler, 1939, is resurrected from the synonymy of S. foetens for one of the S. foetens genetic lineages. The 2 species differ in length and shape of the snout, number of anal-fin rays, and shape of the
anterior-nostril flap. Synodus bondi and S. foetens co-occur in the central Caribbean, but S. bondi otherwise has a more southerly distribution than does S. foetens. Redescriptions are provided for S. intermedius, S. foetens, and S. bondi. Neotypes are designated for S. intermedius and S. foetens. A revised key to Synodus species in the western Atlantic is presented
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A new species of western Atlantic lizardfish (Teleostei: Synodontidae: Synodus) and resurrection of Synodus bondi Fowler, 1939, as a valid species from the Caribbean with redescriptions of S. bondi, S. foetens (Linnaeus, 1766), and S. intermedius (Agassiz, 1829)
Western Atlantic synodontid species were studied as part of an ongoing effort to reanalyze Caribbean shorefish diversity. A neighbor-joining tree constructed from cytochrome c oxidase I (COI) data revealed 2 highly divergent genetic lineages within both Synodus intermedius (Agassiz, 1829) (Sand Diver) and S. foetens (Linnaeus, 1766) (Inshore Lizardfish). A new species, Synodus macrostigmus, is described for one of the S. intermedius lineages. Synodus macrostigmus and S. intermedius differ in number of lateral-line scales, caudal pigmentation, size of the scapular blotch, and shape of the anterior-nostril flap. Synodus macrostigmus and S. intermedius have overlapping geographic and depth distributions, but S. macrostigmus generally inhabits deeper water (>28 m) than does S. intermedius and is known only from coastal waters of the southeastern United States and the Gulf of Mexico, in contrast to those areas and the Caribbean for S. intermedius. Synodus bondi Fowler, 1939, is resurrected from the synonymy of S. foetens for one of the S. foetens genetic lineages. The 2 species differ in length and shape of the snout, number of anal-fin rays, and shape of the anterior-nostril flap. Synodus bondi and S. foetens co-occur in the central Caribbean, but S. bondi otherwise has a more southerly distribution than does S. foetens. Redescriptions are provided for S. intermedius, S. foetens, and S. bondi. Neotypes are designated for S. intermedius and S. foetens. A revised key to Synodus species in the western Atlantic is presented.Keywords: Speciation, Genetics, DNA barcodes, Morphology, Gulf of Mexico, Fish collectionKeywords: Speciation, Genetics, DNA barcodes, Morphology, Gulf of Mexico, Fish collectio
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A new species of Sebastes (Scorpaeniformes: Sebastidae) from the northeastern Pacific, with a redescription of the blue rockfish, S. mystinus (Jordan and Gilbert, 1881)
The diverse predatory rockfishes (Sebastes spp.) support extensive commercial fisheries in the northeastern Pacific. Although 106 species of Sebastes are considered valid, many of the ecological, geographical, and morphological boundaries separating them lack clarity. We clarify one such boundary by separating the blue rockfish Sebastes mystinus (Jordan and Gilbert, 1881) into 2 species on the basis of molecular and morphological data. We redescribe S. mystinus, designate a lectotype, and describe the deacon rockfish, Sebastes diaconus n. sp. Aside from its unambiguous distinction at 6 microsatellite loci, the new species is most easily differentiated from S. mystinus by its possession of a solid in contrast with a blotched color pattern. Sebastes diaconus also possesses a prominent symphyseal knob versus a reduced or absent knob, a flat rather than rounded ventrum, and longer first and second anal-fin spines. Se bastes diaconus occurs from central California northward to British Columbia, Canada, and S. mystinus occurs from northern Oregon south to Baja California Sur, Mexico, indicating a broad region of sympatry in Oregon and northern California. Further collection and study are necessary to clarify distributional boundaries and to understand the ecology and mechanisms of segregation for this species. Additionally, fisheries assessments will need revision to account for the longstanding conflation of these 2 species.This is the publisher’s final pdf. The published article is copyrighted by United States Department of Commerce, National Oceanic and Atmospheric Administration, National Marine Fisheries Service and can be found at: http://fisherybulletin.nmfs.noaa.gov
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Tempo and Mode of Diversification in the Neotropical Fish Superfamily Anostomoidea (Ostariophysi: Characiformes)
Neotropical characiform fishes form one of the most diverse freshwater ichthyofauna in the world. Knowledge of evolutionary processes that generated and maintain the immense characiform lineage and morphological diversity is still poorly understood. When did characiform lineages diversify? How have major geological and environmental changes affected diversification? Why are some clades seemingly more morphologically diverse than others? I examine the characiform superfamily Anostomoidea to address these broader questions of Neotropical diversification.
The abundant Neotropical freshwater fish superfamily Anostomoidea contains two clades with seemingly disparate evolutionary strategies. The first group, the anostomids, represent ~150 species with a wide variety of body coloration, mouth position, tooth shape and trophic strategies ranging from generalist to herbivory to insectivory. The other major group, the families: Curimatidae, Chilodontidae and Prochilodontidae, contains around the same number of species but members are silvery with some pigmentation, have little variation in mouth position, possess reduced or no teeth and all feed mostly on detritus.
The Prochilodontidae are some of the most abundant fish by biomass in South America and participate in mass-migrations for spawning and feeding. This group is characterized by low morphological diversity, large-body size and is generally resilient to small-scale vicariance barriers. As such, I use this widespread family to investigate the influence of large-scale paleoecological events, such as the rise of the Andean Eastern Cordilleras, on diversification of Neotropical fishes. I estimated the first time-calibrated molecular phylogeny for the family Prochilodontidae and compared diversification rate and events with known paleoecological events. Vicariance barriers and other events significantly impacted the historical biogeography of Prochilodontidae, supporting their role in generating the astounding diversity of Neotropical fishes.
In the second part, I investigated whether the morphologically depauperate detritivore clade actually contains a high number of ecologically equivalent species or if they are diversifying in a previously unstudied manner. There is substantially more variation in the arrangement of the gill arches, which are used in processing food, within the detritivores than in the trophically-diverse anostomids. The two clades have evolved over similar amounts of time, but differ in how efficiently they developed new gill morphologies. Through cladogenesis, detritivorous lineages evolved significantly different morphologies more readily and potentially more frequently than the anostomids. The significant diversity and evolutionary pattern of detritivore gill arch shape indicates that selection is acting on how they process food and demonstrates that detritivory encompasses a spectrum of ecomorphological specialization
FIGURE 6 in New specimens and supplementary descriptions of two rare dragonfishes Photonectes klepadloae and P. litvinovi, with comments on the distribution of P filipendulus (Teleostei: Stomiidae: Melanostomiinae)
FIGURE 6. Photonectes litvinovi, schematic of blue-tissue pattern. (?) Connection between midventral bands on isthmus and vent is uncertain due to abrasion of the skin.Published as part of Prokofiev, Artem M. & Frable, Benjamin W., 2023, New specimens and supplementary descriptions of two rare dragonfishes Photonectes klepadloae and P. litvinovi, with comments on the distribution of P filipendulus (Teleostei: Stomiidae: Melanostomiinae), pp. 489-500 in Zootaxa 5228 (4) on page 494, DOI: 10.11646/zootaxa.5228.4.7, http://zenodo.org/record/754013
FIGURE 4 in New specimens and supplementary descriptions of two rare dragonfishes Photonectes klepadloae and P. litvinovi, with comments on the distribution of P filipendulus (Teleostei: Stomiidae: Melanostomiinae)
FIGURE 4. Map of distribution of Photonectes klepadloae (squares), P. litvinovi (triangles) and P. filipendulus (circles); holotypes, solid symbols; other specimens, open symbols.Published as part of Prokofiev, Artem M. & Frable, Benjamin W., 2023, New specimens and supplementary descriptions of two rare dragonfishes Photonectes klepadloae and P. litvinovi, with comments on the distribution of P filipendulus (Teleostei: Stomiidae: Melanostomiinae), pp. 489-500 in Zootaxa 5228 (4) on page 493, DOI: 10.11646/zootaxa.5228.4.7, http://zenodo.org/record/754013