Euteleostei = Ostariophysi + Protacanthoppterygii + Neoteleosts
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The Phylogeny of Oncorhynchus (Euteleostei: Salmonidae) Based on Behavioral and Life History Characters
Copeia, 2007(3), pp. 520–533 The Phylogeny of Oncorhynchus (Euteleostei: Salmonidae) Based on Behavioral and Life History Characters MANU ESTEVE AND DEBORAH A. MCLENNAN There is no consensus between morphological and molecular data concerning the relationships within the Pacific basin salmon and trout clade Oncorhynchus. In this paper we add another source of characters to the discussion. Phylogenetic analysis of 39 behavioral and life history traits produced one tree structured (O. clarki (O. mykiss (O. masou (O. kisutch (O. tshawytscha (O. nerka (O. keta, O. gorbuscha))))))). This topology is congruent with the phylogeny based upon Bayesian analysis of all available nuclear and mitochondrial gene sequences, with the exception of two nodes: behavior supports the morphological data in breaking the sister-group relationship between O. mykiss and O. clarki, and between O. kisutch and O. tshawytscha. The behavioral traits agreed with molecular rather than morphological data in placing O. keta as the sister-group of O. gorbuscha. The behavioral traits also resolve the molecular-based ambiguity concerning the placement of O. masou, placing it as sister to the rest of the Pacific basin salmon. Behavioral plus morphological data placed Salmo, not Salvelinus, as more closely related to Oncorhynchus, but that placement was only weakly supported and awaits collection of missing data from enigmatic species such as the lake trout, Salvelinus namaycush. Overall, the phenotypic characters helped resolve ambiguities that may have been created by molecular introgression, while the molecular traits helped resolve ambiguities introduced by phenotypic homoplasy. It seems reasonable therefore, that systematists can best respond to the escalating biodiversity crisis by forming research groups to gather behavioral and ecological information while specimens are being collected for morphological and molecular analysis. -
Atheriniformes : Atherinidae
Atheriniformes: Atherinidae 2111 Atheriniformes: Atherinidae Order ATHERINIFORMES ATHERINIDAE Silversides by L. Tito de Morais, IRD/LEMAR, University of Brest, Plouzané, France; M. Sylla, Centre de Recherches Océanographiques de Dakar-Thiaroye (CRODT), Senegal and W. Ivantsoff (retired), Biology Science, Macquarie University NSW 2109, North Ryde, Australia iagnostic characters: Small, elongate fish, rarely exceeding 15 cm in length. Body elongate and Dsomewhat compressed. Short head, generally flattened dorsally, large eyes, sharp nose, mouth small, oblique and in terminal position, jaws subequal, reaching or slightly exceeding the anterior margin of the eye; premaxilla with ascending process of variable length, with lateral process present or absent; ramus of dentary bone elevated posteriorly or indistinct from anterior part of lower jaw; fine, small and sharp teeth on the jaws, on the roof of mouth (vomer, palatine, pterygoid) or on outside of mouth; 10 to 26 gill rakers long and slender on lower arm of first gill arch. Two well-separated dorsal fins, the first with 6 to 10 thin, flexible spines, located approximately in the middle of the body; the second dorsal and anal fins with a single small weak spine, 1 unbranched soft ray and a variable number of soft rays. Anal fin always originating slightly in advance of second dorsal fin; pectoral fins inserted high on the flanks, directly behind posterior rim of gill cover, with spine greatly reduced and first ray much thicker than those following. Abdomninal pelvic fins with 1 spine and 5 soft rays; forked caudal fin; anus away from the origin of the anal fin. Relatively large scales, cycloid (smooth). -
BONY FISHES 602 Bony Fishes
click for previous page BONY FISHES 602 Bony Fishes GENERAL REMARKS by K.E. Carpenter, Old Dominion University, Virginia, USA ony fishes constitute the bulk, by far, of both the diversity and total landings of marine organisms encoun- Btered in fisheries of the Western Central Atlantic.They are found in all macrofaunal marine and estuarine habitats and exhibit a lavish array of adaptations to these environments. This extreme diversity of form and taxa presents an exceptional challenge for identification. There are 30 orders and 269 families of bony fishes presented in this guide, representing all families known from the area. Each order and family presents a unique suite of taxonomic problems and relevant characters. The purpose of this preliminary section on technical terms and guide to orders and families is to serve as an introduction and initial identification guide to this taxonomic diversity. It should also serve as a general reference for those features most commonly used in identification of bony fishes throughout the remaining volumes. However, I cannot begin to introduce the many facets of fish biology relevant to understanding the diversity of fishes in a few pages. For this, the reader is directed to one of the several general texts on fish biology such as the ones by Bond (1996), Moyle and Cech (1996), and Helfman et al.(1997) listed below. A general introduction to the fisheries of bony fishes in this region is given in the introduction to these volumes. Taxonomic details relevant to a specific family are explained under each of the appropriate family sections. The classification of bony fishes continues to transform as our knowledge of their evolutionary relationships improves. -
Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi
Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 (http://www.accessscience.com/) Article by: Boschung, Herbert Department of Biological Sciences, University of Alabama, Tuscaloosa, Alabama. Gardiner, Brian Linnean Society of London, Burlington House, Piccadilly, London, United Kingdom. Publication year: 2014 DOI: http://dx.doi.org/10.1036/1097-8542.680400 (http://dx.doi.org/10.1036/1097-8542.680400) Content Morphology Euteleostei Bibliography Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi The most recent group of actinopterygians (rayfin fishes), first appearing in the Upper Triassic (Fig. 1). About 26,840 species are contained within the Teleostei, accounting for more than half of all living vertebrates and over 96% of all living fishes. Teleosts comprise 517 families, of which 69 are extinct, leaving 448 extant families; of these, about 43% have no fossil record. See also: Actinopterygii (/content/actinopterygii/009100); Osteichthyes (/content/osteichthyes/478500) Fig. 1 Cladogram showing the relationships of the extant teleosts with the other extant actinopterygians. (J. S. Nelson, Fishes of the World, 4th ed., Wiley, New York, 2006) 1 of 9 10/7/2015 1:07 PM Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 Morphology Much of the evidence for teleost monophyly (evolving from a common ancestral form) and relationships comes from the caudal skeleton and concomitant acquisition of a homocercal tail (upper and lower lobes of the caudal fin are symmetrical). This type of tail primitively results from an ontogenetic fusion of centra (bodies of vertebrae) and the possession of paired bracing bones located bilaterally along the dorsal region of the caudal skeleton, derived ontogenetically from the neural arches (uroneurals) of the ural (tail) centra. -
Age, Growth and Body Condition of Big-Scale Sand Smelt Atherina Boyeri Risso, 1810 Inhabiting a Freshwater Environment: Lake Trasimeno (Italy)
Knowledge and Management of Aquatic Ecosystems (2015) 416, 09 http://www.kmae-journal.org c ONEMA, 2015 DOI: 10.1051/kmae/2015005 Age, growth and body condition of big-scale sand smelt Atherina boyeri Risso, 1810 inhabiting a freshwater environment: Lake Trasimeno (Italy) M. Lorenzoni(1), D. Giannetto(2),,A.Carosi(1), R. Dolciami(3), L. Ghetti(4), L. Pompei(1) Received September 24, 2014 Revised January 29, 2015 Accepted January 29, 2015 ABSTRACT Key-words: The age, growth and body condition of the big-scale sand smelt (Athe- Population rina boyeri) population of Lake Trasimeno were investigated. In total, dynamics, 3998 specimens were collected during the study and five age classes Lee’s (from 0+ to 4+) were identified. From a subsample of 1017 specimens, phenomenon, there were 583 females, 411 males and 23 juveniles. The equations = − fishery between total length (TL) and weight (W) were: log10 W 2.326 + = − management, 3.139 log10 TL for males and log10 W 2.366 + 3.168 log10 TL for fe- introduced males. There were highly significant differences between the sexes and species, for both sexes the value of b (slope of the log (TL-W regression) was Lake Trasimeno greater than 3 (3.139 for males and 3.168 for females), indicating positive allometric growth. The parameters of the theoretical growth curve were: −1 TLt = 10.03 cm; k = 0.18 yr , t0 = −0.443 yr and Φ = 1.65. Monthly trends of overall condition and the gonadosomatic index (GSI) indicated that the reproductive period occurred from March to September. Analy- sis of back-calculated lengths indicated the occurrence of a reverse Lee’s phenomenon. -
Appendix 1. (Online Supplementary Material) Species, Gliding Strategies
Appendix 1. (Online Supplementary Material) Species, gliding strategies, species distributions, geographic range sizes, habitat, and egg buoyancy characteristics used for concentrated changes tests. Species Gliding strategy Species distribution (reference #) Geographic range size Habitat (reference #) Egg buoyancy (reference #) Cheilopogon abei (Parin, 1996) 4 wings Indian, Indo-Pacific (1) 2 or more ocean basins meroepipelagic (1) Buoyant (2) Cheilopogon atrisignis (Jenkins, 1903) 4 wings Indian, Pacific (1) 2 or more ocean basins meroepipelgic (3) Buoyant (4) Cheilopogon cyanopterus (Valenciennes, 1847) 4 wings Atlantic, Indo-Pacific (2) 2 or more ocean basins meroepipelgic (3) Non-Buoyant (5) Cheilopogon dorsomacula (Fowler, 1944) 4 wings Pacific (1) within 1 ocean basin holoepipelagic (1) Buoyant (2) Cheilopogon exsiliens (Linnaeus, 1771) 4 wings Atlantic (2) within 1 ocean basin holoepipelagic (3) Buoyant (2,5) Cheilopogon furcatus (Mitchill, 1815) 4 wings Atlantic, Indian, Pacific (6) 2 or more ocean basins holoepipelagic (3) Non-Buoyant (5) Cheilopogon melanurus (Valenciennes, 1847) 4 wings Atlantic (7) within 1 ocean basin meroepipelagic (7) Non-Buoyant (5,8) Cheilopogon pinnatibarbatus (californicus) (Cooper, 1863) 4 wings eastern tropical Pacific (9) within 1 ocean basin meroepipelgic (3) Non-Buoyant (10) Cheilopogon spilonotopterus (Bleeker, 1865) 4 wings Indian and Pacific (1) 2 or more ocean basins meroepipelgic (3) Buoyant (4) Cheilopogon xenopterus (Gilbert, 1890) 4 wings eastern tropical Pacific (11) within 1 ocean basin -
CHECKLIST and BIOGEOGRAPHY of FISHES from GUADALUPE ISLAND, WESTERN MEXICO Héctor Reyes-Bonilla, Arturo Ayala-Bocos, Luis E
ReyeS-BONIllA eT Al: CheCklIST AND BIOgeOgRAphy Of fISheS fROm gUADAlUpe ISlAND CalCOfI Rep., Vol. 51, 2010 CHECKLIST AND BIOGEOGRAPHY OF FISHES FROM GUADALUPE ISLAND, WESTERN MEXICO Héctor REyES-BONILLA, Arturo AyALA-BOCOS, LUIS E. Calderon-AGUILERA SAúL GONzáLEz-Romero, ISRAEL SáNCHEz-ALCántara Centro de Investigación Científica y de Educación Superior de Ensenada AND MARIANA Walther MENDOzA Carretera Tijuana - Ensenada # 3918, zona Playitas, C.P. 22860 Universidad Autónoma de Baja California Sur Ensenada, B.C., México Departamento de Biología Marina Tel: +52 646 1750500, ext. 25257; Fax: +52 646 Apartado postal 19-B, CP 23080 [email protected] La Paz, B.C.S., México. Tel: (612) 123-8800, ext. 4160; Fax: (612) 123-8819 NADIA C. Olivares-BAñUELOS [email protected] Reserva de la Biosfera Isla Guadalupe Comisión Nacional de áreas Naturales Protegidas yULIANA R. BEDOLLA-GUzMáN AND Avenida del Puerto 375, local 30 Arturo RAMíREz-VALDEz Fraccionamiento Playas de Ensenada, C.P. 22880 Universidad Autónoma de Baja California Ensenada, B.C., México Facultad de Ciencias Marinas, Instituto de Investigaciones Oceanológicas Universidad Autónoma de Baja California, Carr. Tijuana-Ensenada km. 107, Apartado postal 453, C.P. 22890 Ensenada, B.C., México ABSTRACT recognized the biological and ecological significance of Guadalupe Island, off Baja California, México, is Guadalupe Island, and declared it a Biosphere Reserve an important fishing area which also harbors high (SEMARNAT 2005). marine biodiversity. Based on field data, literature Guadalupe Island is isolated, far away from the main- reviews, and scientific collection records, we pres- land and has limited logistic facilities to conduct scien- ent a comprehensive checklist of the local fish fauna, tific studies. -
Edna Assay Development
Environmental DNA assays available for species detection via qPCR analysis at the U.S.D.A Forest Service National Genomics Center for Wildlife and Fish Conservation (NGC). Asterisks indicate the assay was designed at the NGC. This list was last updated in June 2021 and is subject to change. Please contact [email protected] with questions. Family Species Common name Ready for use? Mustelidae Martes americana, Martes caurina American and Pacific marten* Y Castoridae Castor canadensis American beaver Y Ranidae Lithobates catesbeianus American bullfrog Y Cinclidae Cinclus mexicanus American dipper* N Anguillidae Anguilla rostrata American eel Y Soricidae Sorex palustris American water shrew* N Salmonidae Oncorhynchus clarkii ssp Any cutthroat trout* N Petromyzontidae Lampetra spp. Any Lampetra* Y Salmonidae Salmonidae Any salmonid* Y Cottidae Cottidae Any sculpin* Y Salmonidae Thymallus arcticus Arctic grayling* Y Cyrenidae Corbicula fluminea Asian clam* N Salmonidae Salmo salar Atlantic Salmon Y Lymnaeidae Radix auricularia Big-eared radix* N Cyprinidae Mylopharyngodon piceus Black carp N Ictaluridae Ameiurus melas Black Bullhead* N Catostomidae Cycleptus elongatus Blue Sucker* N Cichlidae Oreochromis aureus Blue tilapia* N Catostomidae Catostomus discobolus Bluehead sucker* N Catostomidae Catostomus virescens Bluehead sucker* Y Felidae Lynx rufus Bobcat* Y Hylidae Pseudocris maculata Boreal chorus frog N Hydrocharitaceae Egeria densa Brazilian elodea N Salmonidae Salvelinus fontinalis Brook trout* Y Colubridae Boiga irregularis Brown tree snake* -
Acanthopterygii, Bone, Eurypterygii, Osteology, Percomprpha
Research in Zoology 2014, 4(2): 29-42 DOI: 10.5923/j.zoology.20140402.01 Comparative Osteology of the Jaws in Representatives of the Eurypterygian Fishes Yazdan Keivany Department of Natural Resources (Fisheries Division), Isfahan University of Technology, Isfahan, 84156-83111, Iran Abstract The osteology of the jaws in representatives of 49 genera in 40 families of eurypterygian fishes, including: Aulopiformes, Myctophiformes, Lampridiformes, Polymixiiformes, Percopsiformes, Mugiliformes, Atheriniformes, Beloniformes, Cyprinodontiformes, Stephanoberyciformes, Beryciformes, Zeiformes, Gasterosteiformes, Synbranchiformes, Scorpaeniformes (including Dactylopteridae), and Perciformes (including Elassomatidae) were studied. Generally, in this group, the upper jaw consists of the premaxilla, maxilla, and supramaxilla. The lower jaw consists of the dentary, anguloarticular, retroarticular, and sesamoid articular. In higher taxa, the premaxilla bears ascending, articular, and postmaxillary processes. The maxilla usually bears a ventral and a dorsal articular process. The supramaxilla is present only in some taxa. The dentary is usually toothed and bears coronoid and posteroventral processes. The retroarticular is small and located at the posteroventral corner of the anguloarticular. Keywords Acanthopterygii, Bone, Eurypterygii, Osteology, Percomprpha following method for clearing and staining bone and 1. Introduction cartilage provided in reference [18]. A camera lucida attached to a Wild M5 dissecting stereomicroscope was used Despite the introduction of modern techniques such as to prepare the drawings. The bones in the first figure of each DNA sequencing and barcoding, osteology, due to its anatomical section are arbitrarily shaded and labeled and in reliability, still plays an important role in the systematic the others are shaded in a consistent manner (dark, medium, study of fishes and comprises a major percent of today’s and clear) to facilitate comparison among the taxa. -
Belonidae Bonaparte 1832 Needlefishes
ISSN 1545-150X California Academy of Sciences A N N O T A T E D C H E C K L I S T S O F F I S H E S Number 16 September 2003 Family Belonidae Bonaparte 1832 needlefishes By Bruce B. Collette National Marine Fisheries Service Systematics Laboratory National Museum of Natural History, Washington, DC 20560–0153, U.S.A. email: [email protected] Needlefishes are a relatively small family of beloniform fishes (Rosen and Parenti 1981 [ref. 5538], Collette et al. 1984 [ref. 11422]) that differ from other members of the order in having both the upper and the lower jaws extended into long beaks filled with sharp teeth (except in the neotenic Belonion), the third pair of upper pharyngeal bones separate, scales on the body relatively small, and no finlets following the dorsal and anal fins. The nostrils lie in a pit anterior to the eyes. There are no spines in the fins. The dorsal fin, with 11–43 rays, and anal fin, with 12–39 rays, are posterior in position; the pelvic fins, with 6 soft rays, are located in an abdominal position; and the pectoral fins are short, with 5–15 rays. The lateral line runs down from the pectoral fin origin and then along the ventral margin of the body. The scales are small, cycloid, and easily detached. Precaudal vertebrae number 33–65, caudal vertebrae 19–41, and total verte- brae 52–97. Some freshwater needlefishes reach only 6 or 7 cm (2.5 or 2.75 in) in total length while some marine species may attain 2 m (6.5 ft). -
Zootaxa, Pisces, Actinopterygii, Cyprinodontiformes, Rivulidae
Zootaxa 928: 1–20 (2005) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 928 Copyright © 2005 Magnolia Press ISSN 1175-5334 (online edition) Kryptolebias sepia n. sp. (Actinopterygii: Cyprinodontiformes: Riv- ulidae), a new killifish from the Tapanahony River drainage in southeast Surinam FRANS B. M. VERMEULEN1 & TOMAS HRBEK2* 1 Tanki Leendert 194 c, Noord, Aruba; [email protected] 2 Department of Biology, University of Puerto Rico Rio Piedras, San Juan, PR 00931, Puerto Rico; [email protected] * Correspondence to: TOMAS HRBEK Abstract Kryptolebias sepia n. sp. is described from small forest tributaries of the Tapanahony and Palumeu Rivers which form part of the Upper Marowijne River system in southeast of Surinam. This species is distinguished from all other Kryptolebias spp. and Rivulus spp. by strong melanism on the body, its ability to change color pattern rapidly, the lack of strong sexual dimorphism, and the presence of pronounced adult/juvenile dichromatism. Key words: Rivulus, Kryptolebias, Guyana Shield, mtDNA, speciation, molecular phylogeny, biodiversity Introduction The fauna and flora of the Guyana shield is particularly rich. While extensive floristic sur- veys have been undertaken, relatively little work has been conducted on the fish fauna of this region. Most surveys have been done in Venezuela, and Brazilian surveys have con- centrated primarily on the middle Rio Negro drainage. The first and last major survey of Guyana was conducted by Eigenmann in 1909 (Eigenmann 1912), and more recently his route has been retraced by researchers focusing on loricariid catfishes (Hardman et al. 2002). A survey of freshwater fishes of French Guiana has also been published (Keith et al. -
A New Species of Cretaceous Acanthomorph from Canada 15 February 2016, by Sarah Gibson
A new species of Cretaceous acanthomorph from Canada 15 February 2016, by Sarah Gibson to sit flush along the body, helping the fish swim faster by reducing drag, or they can be extended completely out to act as a defense mechanism, in case you are a predator looking for a quick bite. Near the base of the Acanthomorpha phylogenetic tree is a small group of fishes, Polymixiiformes, comprised of a single living genus, Polymixia, more commonly known as the beardfish. This innocuous fish seems harmless, but according to many ichthyologists, Polymixia is just one key to understanding acanthomorph relationships. Unraveling the evolutionary relationships is difficult with a single living genus, but thankfully, polymixiiforms have a fossil record dating back to the Cretaceous, containing an increasing number of taxa as new discoveries are being made, particularly in deposits in North America, where fewer acanthomorph fossils are known compared to Figuring out fish relationships is no small feat. Credit: the more-studied Eastern Tethys Ocean deposits in Near et al. 2013 Europe. For being one of the largest groups of vertebrates, and having one of the richer fossil records among organisms, the relationships of fishes are still hotly debated. Humongous datasets are being compiled that involve molecular (both nuclear and mitochondrial) data, compared and contrasted with thorough morphological analyses. (I'm not going to get into all of it here, simply because of its sheer complexity.) What I am going to get into, however, is the fossil record of one subset of fishes, the acanthomorphs. The stout beardfish, Polymixia nobilis. Credit: Wikipedia Acanthomorphs are teleost fishes that possess true fin spines: a set of prominent, sharp, unsegmented spines in the front portion of their dorsal and/or anal fins, followed by a portion of One such new species was recently described by pliable, segmented, "softer" looking rays.