UNIVERSITY of CALIFORNIA RIVERSIDE the Evolution of Reproductive Mode and Its Effect on Speciation in Cyprinodontiform Fishes A
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Historical Biogeography of Cynolebiasine Annual Killifishes
Journal of Biogeography (J. Biogeogr.) (2010) 37, 1995–2004 ORIGINAL Historical biogeography of cynolebiasine ARTICLE annual killifishes inferred from dispersal–vicariance analysis Wilson J. E. M. Costa* Laborato´rio de Sistema´tica e Evoluc¸a˜ode ABSTRACT Peixes Teleo´steos, Departamento de Zoologia, Aim To analyse the biogeographical events responsible for the present Universidade Federal do Rio de Janeiro, Caixa Postal 68049, CEP 21944-970, Rio de Janeiro, distribution of cynolebiasine killifishes (Teleostei: Rivulidae: Cynolebiasini), RJ, Brazil a diversified and widespread Neotropical group of annual fishes threatened with extinction. Location South America, focusing on the main river basins draining the Brazilian Shield and adjacent zones. Methods Phylogenetic analysis of 214 morphological characters of 102 cynolebiasine species using tnt, in conjunction with dispersal–vicariance analysis (diva) based on the distribution of cynolebiasine species among 16 areas of endemism. Results The basal cynolebiasine node is hypothesized to be derived from an old vicariance event occurring just after the separation of South America from Africa, when the terrains at the passive margin of the South American plate were isolated from the remaining interior areas. This would have been followed by geodispersal events caused by river-capturing episodes from the adjacent upland river basins to the coastal region. Optimal ancestral reconstructions suggest that the diversification of the tribe Cynolebiasini in north-eastern South America was first caused by vicariance events in the Parana˜–Urucuia–Sa˜o Francisco area, followed by dispersal from the Sa˜o Francisco to the Northeastern Brazil area. The latter dispersal event occurred simultaneously in two different cynolebiasine clades, possibly as a result of a temporary connection of the Sa˜o Francisco area before the uplift of the Borborema Plateau during the Miocene. -
2017 JMIH Program Book Web Version 6-26-17.Pub
Organizing Societies American Elasmobranch Society 33rd Annual Meeting President: Dean Grubbs Treasurer: Cathy Walsh Secretary: Jennifer Wyffels Editor and Webmaster: David Shiffman Immediate Past President: Chris Lowe American Society of Ichthyologists and Herpetologists 97th Annual Meeting President: Carole Baldwin President Elect: Brian Crother Past President: Maureen A. Donnelly Prior Past President: Larry G. Allen Treasurer: F. Douglas Martin Secretary: Prosanta Chakrabarty Editor: Christopher Beachy Herpetologists’ League 75th Annual Meeting President: David M. Green Immediate Past President: James Spotila Vice-President: David Sever Treasurer: Laurie Mauger Secretary: Renata Platenburg Publications Secretary: Ken Cabarle Communications Secretary: Wendy Palin Herpetologica Editor: Stephen Mullin Herpetological Monographs Editor: Michael Harvey Society for the Study of Amphibians and Reptiles 60th Annual Meeting President: Richard Shine President-Elect: Marty Crump Immediate Past-President: Aaron Bauer Secretary: Marion R. Preest Treasurer: Kim Lovich Publications Secretary: Cari-Ann Hickerson Thank you to our generous sponsor We would like to thank the following: Local Hosts David Hillis, University of Texas at Austin, LHC Chair Dean Hendrickson, University of Texas at Austin Becca Tarvin, University of Texas at Austin Anne Chambers, University of Texas at Austin Christopher Peterson, University of Texas at Austin Volunteers We wish to thank the following volunteers who have helped make the Joint Meeting of Ichthyologists and Herpetologists -
FAMILY Poeciliidae Bonaparte 1831
FAMILY Poeciliidae Bonaparte 1831 - viviparous toothcarps, livebearers SUBFAMILY Poeciliinae Bonaparte 1831 - viviparous toothcarps [=Unipupillati, Paecilini, Belonesocini, Cyprinodontidae limnophagae, Gambusiinae, Tomeurinae, Poeciliopsinae, Heterandriini, Guirardinini, Cnesterodontini, Pamphoriini, Xiphophorini, Alfarini, Quintanini, Xenodexiinae, Dicerophallini, Scolichthyinae, Priapellini, Brachyrhaphini, Priapichthyini] GENUS Alfaro Meek, 1912 - livebearers [=Furcipenis, Petalosoma, Petalurichthys] Species Alfaro cultratus (Regan, 1908) - Regan's alfaro [=acutiventralis, amazonum] Species Alfaro huberi (Fowler, 1923) - Fowler's alfaro GENUS Belonesox Kner, 1860 - pike topminnows Species Belonesox belizanus Kner, 1860 - pike topminnow [=maxillosus] GENUS Brachyrhaphis Regan, 1913 - viviparous toothcarps [=Plectrophallus, Trigonophallus] Species Brachyrhaphis cascajalensis (Meek & Hildebrand, 1913) - Río Cascajal toothcarp Species Brachyrhaphis episcopi (Steindachner, 1878) - Obispo toothcarp [=latipunctata] Species Brachyrhaphis hartwegi Rosen & Bailey, 1963 - Soconusco gambusia Species Brachyrhaphis hessfeldi Meyer & Etzel, 2001 - Palenque toothcarp Species Brachyrhaphis holdridgei Bussing, 1967 - Tronadora toothcarp Species Brachyrhaphis olomina (Meek, 1914) - Orotina toothcarp Species Brachyrhaphis parismina (Meek, 1912) - Parismina toothcarp Species Brachyrhaphis punctifer (Hubbs, 1926) - Quibari Creek toothcarp Species Brachyrhaphis rhabdophora (Regan, 1908) - Río Grande de Terraba toothcarp [=tristani] Species Brachyrhaphis roseni -
Strong Reproductive Skew Among Males in the Multiply Mated Swordtail Xiphophorus Multilineatus (Teleostei)
Journal of Heredity 2005:96(4):346–355 ª The American Genetic Association. 2005. All rights reserved. doi:10.1093/jhered/esi042 For Permissions, please email: [email protected]. Advance Access publication March 2, 2005 Strong Reproductive Skew Among Males in the Multiply Mated Swordtail Xiphophorus multilineatus (Teleostei) J. LUO,M.SANETRA,M.SCHARTL, AND A. MEYER From Fachbereich Biologie, Universita¨t Konstanz, 78457 Konstanz, Germany (Luo, Sanetra, and Meyer); and Physiologische Chemie I, Biozentrum der Universita¨t, Am Hubland, 97074 Wu¨rzburg, Germany (Schartl). Address correspondence to Axel Meyer, Fachbereich Biologie, Universita¨t Konstanz, Fach M617, Universita¨tsstrasse 10, 78457 Konstanz, Germany, or e-mail: [email protected]. Abstract Male swordtails in the genus Xiphophorus display a conspicuous ventral elongation of the caudal fin, the sword, which arose through sexual selection due to female preference. Females mate regularly and are able to store sperm for at least 6 months. If multiple mating is frequent, this would raise the intriguing question about the role of female choice and male-male competition in shaping the mating system of these fishes. Size-dependent alternate mating strategies occur in Xiphophorus; one such strategy is courtship with a sigmoid display by large dominant males, while the other is gonopodial thrusting, in which small subordinate males sneak copulations. Using microsatellite markers, we observed a frequency of multiple paternity in wild-caught Xiphophorus multilineatus in 28% of families analyzed, but the actual frequency of multiple mating suggested by the correction factor PrDM was 33%. The number of fathers contributing genetically to the brood ranged from one to three. -
The Evolution of the Placenta Drives a Shift in Sexual Selection in Livebearing Fish
LETTER doi:10.1038/nature13451 The evolution of the placenta drives a shift in sexual selection in livebearing fish B. J. A. Pollux1,2, R. W. Meredith1,3, M. S. Springer1, T. Garland1 & D. N. Reznick1 The evolution of the placenta from a non-placental ancestor causes a species produce large, ‘costly’ (that is, fully provisioned) eggs5,6, gaining shift of maternal investment from pre- to post-fertilization, creating most reproductive benefits by carefully selecting suitable mates based a venue for parent–offspring conflicts during pregnancy1–4. Theory on phenotype or behaviour2. These females, however, run the risk of mat- predicts that the rise of these conflicts should drive a shift from a ing with genetically inferior (for example, closely related or dishonestly reliance on pre-copulatory female mate choice to polyandry in conjunc- signalling) males, because genetically incompatible males are generally tion with post-zygotic mechanisms of sexual selection2. This hypoth- not discernable at the phenotypic level10. Placental females may reduce esis has not yet been empirically tested. Here we apply comparative these risks by producing tiny, inexpensive eggs and creating large mixed- methods to test a key prediction of this hypothesis, which is that the paternity litters by mating with multiple males. They may then rely on evolution of placentation is associated with reduced pre-copulatory the expression of the paternal genomes to induce differential patterns of female mate choice. We exploit a unique quality of the livebearing fish post-zygotic maternal investment among the embryos and, in extreme family Poeciliidae: placentas have repeatedly evolved or been lost, cases, divert resources from genetically defective (incompatible) to viable creating diversity among closely related lineages in the presence or embryos1–4,6,11. -
The Etyfish Project © Christopher Scharpf and Kenneth J
CYPRINODONTIFORMES (part 3) · 1 The ETYFish Project © Christopher Scharpf and Kenneth J. Lazara COMMENTS: v. 3.0 - 13 Nov. 2020 Order CYPRINODONTIFORMES (part 3 of 4) Suborder CYPRINODONTOIDEI Family PANTANODONTIDAE Spine Killifishes Pantanodon Myers 1955 pan(tos), all; ano-, without; odon, tooth, referring to lack of teeth in P. podoxys (=stuhlmanni) Pantanodon madagascariensis (Arnoult 1963) -ensis, suffix denoting place: Madagascar, where it is endemic [extinct due to habitat loss] Pantanodon stuhlmanni (Ahl 1924) in honor of Franz Ludwig Stuhlmann (1863-1928), German Colonial Service, who, with Emin Pascha, led the German East Africa Expedition (1889-1892), during which type was collected Family CYPRINODONTIDAE Pupfishes 10 genera · 112 species/subspecies Subfamily Cubanichthyinae Island Pupfishes Cubanichthys Hubbs 1926 Cuba, where genus was thought to be endemic until generic placement of C. pengelleyi; ichthys, fish Cubanichthys cubensis (Eigenmann 1903) -ensis, suffix denoting place: Cuba, where it is endemic (including mainland and Isla de la Juventud, or Isle of Pines) Cubanichthys pengelleyi (Fowler 1939) in honor of Jamaican physician and medical officer Charles Edward Pengelley (1888-1966), who “obtained” type specimens and “sent interesting details of his experience with them as aquarium fishes” Yssolebias Huber 2012 yssos, javelin, referring to elongate and narrow dorsal and anal fins with sharp borders; lebias, Greek name for a kind of small fish, first applied to killifishes (“Les Lebias”) by Cuvier (1816) and now a -
Fish Larvae, Development, Allometric Growth, and the Aquatic Environment
II. Developmental and environmental interactions ICES mar. Sei. Symp., 201: 21-34. 1995 Fish larvae, development, allometric growth, and the aquatic environment J. W. M. Osse and J. G. M. van den Boogaart Osse, J. W. M., and van den Boogaart, J. G. M. 1995. Fish larvae, development, allometric growth, and the aquatic environment. - ICES mar. Sei. Symp., 201: 21-34. During metamorphosis, fish larvae undergo rapid changes in external appearance and dimensions of body parts. The juveniles closely resemble the adult form. The focus of the present paper is the comparison of stages of development of fishes belonging within different taxa in a search for general patterns. The hypothesis that these patterns reflect the priorities of vital functions, e.g., feeding, locomotion, and respiration, is tested taking into account the size-dependent influences of the aquatic environment on the larvae. A review of some literature on ailometries of fish larvae is given and related to the rapidly changing balance between inertial and viscous forces in relation to body length and swimming velocity. New data on the swimming of larval and juvenile carp are presented. It is concluded that the patterns of development and growth shows in many cases a close parallel with the successive functional requirements. J. W. M. Osse and J. G. M. van den Boogaart: Wageningen Agricultural University, Department of Experimental Animal Morphology and Cell Biology, Marijkeweg 40, 6709 PG Wageningen, The Netherlands [tel: (+31) (0)317 483509, fax: (+31) (0)317 483962], Introduction Fish larvae, being so small, must have problems using their limited resources for maintenance, activity, obtain Fish larvae are the smallest free-living vertebrates. -
Uncorrected Proofs for Review Only C5478.Indb 28 1/24/11 2:08:33 PM M
Chapter 3 Variation and evolution of reproductive strategies Marcelo N. Pires, Amanda Banet, Bart J. A. Pollux, and David N. Reznick 3.1 Introduction sociation between these two traits suggests that one of the two traits might be more likely to evolve when the other he family poeciliidae (Rosen & Bailey 1963) trait is already present (the latter facilitating the evolu- consists of a well-defi ned, monophyletic group of tion of the former). However, the existence of a notable Tnearly 220 species with a fascinating heterogene- exception in the literature (the lecithotrophic, superfetat- ity in life-history traits. Reznick and Miles (1989a) made ing Poeciliopsis monacha, the only known exception at the one of the fi rst systematic attempts to gather information time) showed that superfetation and matrotrophy were not from a widely scattered literature on poeciliid life histo- strictly linked, indicating that these two traits can evolve ries. They focused on two important female reproductive independently of each other. traits: (1) the ability to carry multiple broods at different Reznick and Miles (1989a) also proposed a framework developmental stages (superfetation; Turner 1937, 1940b, for future research that was aimed at evaluating possible 1940c), which tends to cause females to produce fewer off- causes and mechanisms for the evolution of superfetation spring per brood and to produce broods more frequently, and matrotrophy by (1) gathering detailed life-history de- and (2) the provisioning of eggs and developing embryos scriptions of a greater number of poeciliid species, either by the mother, which may occur prior to (lecithotrophy) or through common garden studies or from fi eld-collected after (matrotrophy) fertilization. -
Reproducción Y Crecimiento De Heterandria Bimaculata
Rev. Biol. Trop., 47(3): 581-592, 1999 www.ucr.ac.cr WWW.ots.ac.cr www.ots.duke.edu Reproducción y crecimiento de Heterandria bimaculata . (Cyprinodontiformes:PoeciUidae) en la LagUIia " EIRo(}eo"; �orelos,�é�co José Luis Gómez-Márquez, José Luis Guzmán-Santiago y Alberto Olvera-Soto Laboratorio de Limnología, Facultad de Estudios Superiores Zaragoza, Campus ll, UNAM. Batalla del 5 de Mayo esq. Fuerte de Loreto, Col. Ejército de Oriente. C.P. 09230, México, D.F. Fax 7 73 01 51, correo electrónico: [email protected] Recibido 11-VIII-1998. Corregido 11-1-1999. Aceptado 15-1-1999. Abstract: We studied reproduction and growth of Heterandria bimaculata in "El Rodeo" lake Morelos, Mexico, from December 1986 through December 1987. A total of 1 452 specimens were obtained (monthly samples). Females represented 60.12 %, males 34.98 % and the young 4.89 % of the population. Overall sex ratio was 1.7: 1 in favor of females (X2 p<0.05). The size at frrst reproduction for females was 27 mm and for males 22 mm (standard lengths); multiple spawning occured throughout the reproductive cycle (from March through May and July through October) primarily, during the rainy season. There was evidence of breeding activity throughout the year. In July thegonadosomatic index mean was highest (4.7%). The numberof embryos in the ovaries were between 5 and 78, with a mean fertility of 23, the fertility was associated with standard length with deterrnina tion coefficients aboye 93.22 percent. There was a direct relationship between specimen length and weight, and the asymptotic size for males was 64 mm and for females 81 mm (standard lengths). -
Table S1.Xlsx
Bone type Bone type Taxonomy Order/series Family Valid binomial Outdated binomial Notes Reference(s) (skeletal bone) (scales) Actinopterygii Incertae sedis Incertae sedis Incertae sedis †Birgeria stensioei cellular this study †Birgeria groenlandica cellular Ørvig, 1978 †Eurynotus crenatus cellular Goodrich, 1907; Schultze, 2016 †Mimipiscis toombsi †Mimia toombsi cellular Richter & Smith, 1995 †Moythomasia sp. cellular cellular Sire et al., 2009; Schultze, 2016 †Cheirolepidiformes †Cheirolepididae †Cheirolepis canadensis cellular cellular Goodrich, 1907; Sire et al., 2009; Zylberberg et al., 2016; Meunier et al. 2018a; this study Cladistia Polypteriformes Polypteridae †Bawitius sp. cellular Meunier et al., 2016 †Dajetella sudamericana cellular cellular Gayet & Meunier, 1992 Erpetoichthys calabaricus Calamoichthys sp. cellular Moss, 1961a; this study †Pollia suarezi cellular cellular Meunier & Gayet, 1996 Polypterus bichir cellular cellular Kölliker, 1859; Stéphan, 1900; Goodrich, 1907; Ørvig, 1978 Polypterus delhezi cellular this study Polypterus ornatipinnis cellular Totland et al., 2011 Polypterus senegalus cellular Sire et al., 2009 Polypterus sp. cellular Moss, 1961a †Scanilepis sp. cellular Sire et al., 2009 †Scanilepis dubia cellular cellular Ørvig, 1978 †Saurichthyiformes †Saurichthyidae †Saurichthys sp. cellular Scheyer et al., 2014 Chondrostei †Chondrosteiformes †Chondrosteidae †Chondrosteus acipenseroides cellular this study Acipenseriformes Acipenseridae Acipenser baerii cellular Leprévost et al., 2017 Acipenser gueldenstaedtii -
Sexual Selection: Placentation, Superfetation, and Coercive Copulation
Sexual Selection: Placentation, Superfetation, and Coercive Copulation The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Haig, David. 2014. “Sexual Selection: Placentation, Superfetation, and Coercive Copulation.” Current Biology 24 (17) (September): R805–R808. doi:10.1016/j.cub.2014.07.039. Published Version doi:10.1016/j.cub.2014.07.039 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:27867248 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Open Access Policy Articles, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#OAP Sexual selection: placentation, superfetation, and coercive copulation. David Haig Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, 02138, United States of America 1 Placentation in poeciliid fishes is associated with conception of overlapping litters and a shift in male mating strategies from less to more coercive. Sperm competition in ovaries of multiply-inseminated females may favor fertilization of immature eggs during ongoing pregnancies. Intersexual selection is commonly described as the process by which female choice of mating partners shapes male attributes to conform to female preferences, but it also encompasses male adaptations to circumvent female choice by deceipt or coercion. The diverse life histories of fish provide many opportunities for exploring this evolutionary dynamic. External fertilization allows a female substantial control over who sires her fry because she determines when (and near whom) her eggs are released, but non-chosen males of many species adopt opportunistic strategies of darting in to release sperm at the moment a female spawns with a chosen male [1]. -
Options for Selectively Controlling Non-Indigenous Fish in the Upper Colorado River Basin
Options for Selectively Controlling Non-Indigenous Fish in the Upper Colorado River Basin Draft Report June 1995 Leo D. Lentsch Native Fish and Herptile Coordinator Utah Division of Wildlife Resources Robert Muth Larval Fish Lab Colorado State University Paul D. Thompson Native Fish Biologist Utah Division of Wildlife Resources Dr. Todd A. Crowl Utah State University and Brian G. Hoskins Native Fish Technician Utah Division of Wildlife Resources Utah Division of Wildlife Resources Colorado River Fishery Project Salt Lake City, Utah TABLE OP CONTENTS PAGE ABSTRACT .......................... INTRODUCTION ...................... Non-Indigenous Problems ..... Objectives ................... Control Options ............. Mechanical Control ..... Chemical Control ....... Biological Control ..... Physicochemical Control METHODS .......................................................... Literature Review .......................................... Species Accounts ........................................... RESULTS .......................................................... Species Accounts ........................................... Clupeidae-Herrings ................................... Threadfin Shad .................................. Cyprinidae-Carps and Minnows ........................ Red Shiner ...................................... Common Carp ..................................... Utah Chub ........................................ Leathers ide Chub ................................ Brassy Minnow ................................... Plains Minnow