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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. -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
Final Report an EVALUATION of the APPLICABILITY of UPLAND
Final Report AN EVALUATION OF THE APPLICABILITY OF UPLAND BUFFERS FOR THE WETLANDS OF THE WEKIVA BASIN Mark T. Brown and Joseph M. Schaefer, Principal Investigators with K. H. Brandt, S. J. Doherty, C. D. Dove, J. P. Dudley, D. A. Eifler, L. D. Harris, R. F. Noss, and R. W. Wolfe October, 1987 Center for Wetlands University of Florida Gainesville, Florida 32611 ( 904) 392 -2424 Acknowledgements The authors wish to express their appreciation to the staff of the Center For Wetlands, for their dedication and service way beyond the call of duty. Their attitude made completion of this report so much easier. Specifically, Jenny Carter, Staff Assistant, coordinated personnel and somehow managed to get the report finalized under difficult odds. Linda J. Crowder processed all the words over and over again as we edited and polished. Carol Cox proofread each draft. Stephen Roguski, our expert draftsperson, drafted the figures. Karla Brandt not only helped with research and writing, but did a fantastic job of final editing. Steven Tennenbaum devoted two days to derivations of the Theis Equation. We thank you for your energy. Ms. Sidney Brinson, spent a day in the field with the authors explaining the Districts methodology for wetlands determination. Staff from the Florida Department of Natural Resources, especially Ms. Deborah Shelly, provided support and transportation, Glenn Lowe, Chief Environmental Specialist a the St. Johns River Water Management District was project manager for the District and was extremely patient and effective in his support. ii Preface This document is the product of a contract between the St. -
THROWTRAP FISH ID GUIDE.V5 Loftusedits
Fish Identification Guide For Throw trap Samples Florida International University Aquatic Ecology Lab April 2007 Prepared by Tish Robertson, Brooke Sargeant, and Raúl Urgellés Table of Contents Basic fish morphology diagrams………………………………………..3 Fish species by family…………………………………………………...4-31 Gar…..………………………………………………………….... 4 Bowfin………….………………………………..………………...4 Tarpon…...……………………………………………………….. 5 American Eel…………………..………………………………….5 Bay Anchovy…..……..…………………………………………...6 Pickerels...………………………………………………………...6-7 Shiners and Minnows…………………………...……………….7-9 Bullhead Catfishes……..………………………………………...9-10 Madtom Catfish…………………………………………………..10 Airbreathing Catfish …………………………………………….11 Brown Hoplo…...………………………………………………….11 Orinoco Sailfin Catfish……………………………..……………12 Pirate Perch…….………………………………………………...12 Topminnows ……………….……………………….……………13-16 Livebearers……………….……………………………….…….. 17-18 Pupfishes…………………………………………………………19-20 Silversides..………………………………………………..……..20-21 Snook……………………………………………………………...21 Sunfishes and Basses……………….……………………....….22-25 Swamp Darter…………………………………………………….26 Mojarra……...…………………………………………………….26 Everglades pygmy sunfish……………………………………...27 Cichlids………………………….….………………………….....28-30 American Soles…………………………………………………..31 Key to juvenile sunfish..………………………………………………...32 Key to cichlids………....………………………………………………...33-38 Note for Reader/References…………………………………………...39 2 Basic Fish Morphology Diagrams Figures from Page and Burr (1991). 3 FAMILY: Lepisosteidae (gars) SPECIES: Lepisosteus platyrhincus COMMON NAME: Florida gar ENP CODE: 17 GENUS-SPECIES -
Okefenokee National Wildlife Refuge Amphibians, Fish, Mammals and Reptiles List
U.S. Fish & Wildlife Service Okefenokee National Wildlife Refuge Amphibians, Fish, Mammals and Reptiles List The Okefenokee swamp is covered with Mammals ___Seminole Bat cypress, blackgum, and bay forests (Lasiurus seminolus). A common bat of scattered throughout a flooded prairie ___Virginia Opossum the Okefenokee which is found hanging in made of grasses, sedges, and various (Didelphis virginiana pigna). Common on Spanish Moss during the day. the swamp edge and the islands within aquatic plants. The peripheral upland and ___Hoary Bat the almost 70 islands within the swamp the Swamp. A night prowler. “Pogo” is often seen by campers. (Lasiurus cinereus cinereus). This are forested with pine interspersed with yellowish-brown bat flies high in the air hardwood hammocks. Lakes of varying ___Southern Short-Tailed Shrew late at night and will hang in trees when sizes and depths, and floating sections (Barina carolinensis). A specimen was resting. It is the largest bat in the East of the peat bed, are also part of the found on Floyds Island June 12, 1921. It and eats mostly moths. Okefenokee terrain. kills its prey with poisonous saliva. ___Northern Yellow Bat People have left their mark on the swamp. ___Least Shrew (Lasiurus intermedius floridanus). A 12-mile long canal was dug into the (Cryptotus parva parva). Rarely seen but Apparently a rare species in the area. It eastern prairies in the 1890’s in a failed probably fairly common. Specimens have likes to feed in groups. attempt to drain the swamp. During the been found on several of the islands, on early 1900’s large amounts of timber were the swamp edge, and in the pine woods ___Evening Bat removed, so that very few areas of virgin around the swamp. -
ERSS-African Jewelfish (Hemichromis Letourneuxi)
African Jewelfish (Hemichromis letourneuxi) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, February 2011 Revised, February 2018, July 2018 Web Version, 7/30/2018 Photo: Noel M. Burkhead – USGS. Available: https://nas.er.usgs.gov/queries/FactSheet.aspx?SpeciesID=457. (February 2018). 1 Native Range and Status in the United States Native Range From Froese and Pauly (2018): “Africa: Nile to Senegal and from North Africa to Côte d'Ivoire [Central African Republic, Chad, Egypt, Ethiopia, Gambia, Ghana, Guinea, Ivory Coast, Kenya, Senegal, Sierra Leone, South Sudan, Sudan; questionable in Algeria].” From Nico et al. (2018): “Tropical Africa. Widespread in northern, central, and west Africa (Loiselle 1979, 1992; Linke and Staeck 1994) in savannah and oasis habitats.” CABI (2018) reports H. letourneuxi as widespread and native in the following countries: Algeria, Burkina Faso, Cameroon, Chad, Egypt, Ethiopia, Gambia, Ghana, Ivory Coast, Kenya, Niger, Nigeria, Senegal, Sudan, and Uganda. 1 Status in the United States From Eschmeyer et al. (2018): “[…] established in Florida, U.S.A.” From Nico et al. (2018): “Established in Florida. Prior to 1972, found only in Miami Canal and canals on western side of Miami International Airport (Hogg 1976a). Species is now abundant and spreading westward and northward.” “The species was first documented as occurring in south Florida in the Hialeah Canal-Miami River Canal system, Miami area, by Rivas (1965). It is now established and abundant in many canals in and around Miami-Dade County, and also in parts of the Everglades freshwater wetlands and tidal habitats (Courtenay et al. 1974; Hogg 1976a, b; Loftus and Kushlan 1987; Loftus et al. -
Appendix A: Equipment & Supplies
National Rivers and Streams Assessment 2018/19 Field Operations Manual Version 1.1 April 2018 Appendix A: Equipment & Supplies T & SUPPLIES & T APPENDIX A: EQUIPMEN A: APPENDIX A-1 National Rivers and Streams Assessment 2018/19 Field Operations Manual Version 1.1 April 2018 T & SUPPLIES & T APPENDIX A: EQUIPMEN A: APPENDIX A-2 National Rivers and Streams Assessment 2018/19 Field Operations Manual Version 1.1 April 2018 Base Kit A Base Kit will be provided to the field crews for all sampling sites that they will go to. Some items are sent in the base kit as extra supplies to be used as needed. Base Kit Item Quantity Protocol Antibiotic Salve 1 Fish Plug Aspirator bulb 1 Fish Plug Beaker (3 L, Nalgene) 1 Water Chemistry Centrifuge tube stand 1 Chlorophyll A Centrifuge tubes (sterile, green screw-top, 50-mL) (10/pack) 1 pack Chlorophyll A Periphyton Chlorophyll bottle (2 L, brown) 1 Chlorophyll A Clinometer† 1 Physical Habitat Compass† 1 Physical Habitat Delimiter – 12 cm2 area 1 Periphyton Densiometer - Convex spherical (modified with taped V)† 1 Physical Habitat D-frame Kick Net (500 µm mesh, 52” handle) † 1 Benthics Dry ice label (Class 9)* 5 Shipping Electrical tape - roll* 1 General FedEx labels, 5 sets of each in file folder (T1, T2, T3, T5)* 1 Shipping Filtration chamber adapter 3 Enterococci, Chlorophyll A, Periphyton Filtration flask 1 Enterococci, Chlorophyll A, Periphyton Filtration flask stopper (silicone, blue) 2 Enterococci, Chlorophyll A, Periphyton Filtration unit (sterile 250 ml funnel, cap and filter holder) - spares 5 Enterococci, -
Pre- and Post-Copulatory Sexual Selection in the Least Killifish, Heterandria Formosa
Pre- and post-copulatory sexual selection in the least killifish, Heterandria formosa Outi Ala-Honkola Department of Biological and Environmental Sciences Faculty of Biosciences University of Helsinki Finland Academic dissertation To be presented for public examination with the permission of the Faculty of Biosciences of the University of Helsinki in the Auditorium 2041 of Biocenter 2, Viikinkaari 5, on October 30th at 12 o’clock noon. Helsinki 2009 Supervisor: Prof. Kai Lindström, Åbo Akademi University, Finland Pre-examiners: Prof. Arja Kaitala, University of Oulu, Finland Dr. Jonathan Evans, University of Western Australia, Australia Opponent: Dr. Tommaso Pizzari, University of Oxford, United Kingdom Custos: Prof. Liselotte Sundström, University of Helsinki, Finland Author’s address: Outi Ala-Honkola Department of Biological and Environmental Sciences P.O.Box 65 (Viikinkaari 1) FI-00014 University of Helsinki Finland e-mail: [email protected] ISBN 978-952-92-6211-3 (paperback) ISBN 978-952-10-5785-4 (pdf) http://ethesis.helsinki.fi Yliopistopaino Helsinki 2009 Typically, the scientific paper or monograph presents an immaculate appearance, which reproduces little or nothing of the intuitive leaps, false starts, mistakes, loose ends, and happy accidents that actually cluttered up the inquiry. (Merton, 1968) Contents Summary .............................................................................................................. 7 1. Introduction ................................................................................................. -
Drainage Basin Checklists and Dichotomous Keys for Inland Fishes of Texas
A peer-reviewed open-access journal ZooKeys 874: 31–45Drainage (2019) basin checklists and dichotomous keys for inland fishes of Texas 31 doi: 10.3897/zookeys.874.35618 CHECKLIST http://zookeys.pensoft.net Launched to accelerate biodiversity research Drainage basin checklists and dichotomous keys for inland fishes of Texas Cody Andrew Craig1, Timothy Hallman Bonner1 1 Department of Biology/Aquatic Station, Texas State University, San Marcos, Texas 78666, USA Corresponding author: Cody A. Craig ([email protected]) Academic editor: Kyle Piller | Received 22 April 2019 | Accepted 23 July 2019 | Published 2 September 2019 http://zoobank.org/B4110086-4AF6-4E76-BDAC-EA710AF766E6 Citation: Craig CA, Bonner TH (2019) Drainage basin checklists and dichotomous keys for inland fishes of Texas. ZooKeys 874: 31–45. https://doi.org/10.3897/zookeys.874.35618 Abstract Species checklists and dichotomous keys are valuable tools that provide many services for ecological stud- ies and management through tracking native and non-native species through time. We developed nine drainage basin checklists and dichotomous keys for 196 inland fishes of Texas, consisting of 171 native fishes and 25 non-native fishes. Our checklists were updated from previous checklists and revised using reports of new established native and non-native fishes in Texas, reports of new fish occurrences among drainages, and changes in species taxonomic nomenclature. We provided the first dichotomous keys for major drainage basins in Texas. Among the 171 native inland fishes, 6 species are considered extinct or extirpated, 13 species are listed as threatened or endangered by U.S. Fish and Wildlife Service, and 59 spe- cies are listed as Species of Greatest Conservation Need (SGCN) by the state of Texas. -
Life History Variation Along a Salinity Gradient in Coastal Marshes
Vol. 8: 15–28, 2009 AQUATIC BIOLOGY Published online December 29 doi: 10.3354/ab00203 Aquat Biol OPENPEN ACCESSCCESS Life history variation along a salinity gradient in coastal marshes Shannon B. Martin1, 2,*, Alan T. Hitch1, 3, Kevin M. Purcell1, 4, Paul L. Klerks1, Paul L. Leberg1 1Department of Biology, University of Louisiana at Lafayette, Lafayette, Louisiana 70504, USA 2Present address: Florida Fish and Wildlife Conservation Commission, Fish and Wildlife Research Institute, Apalachicola Field Laboratory, Eastpoint, Florida 32328, USA 3Present address: School of Forestry and Wildlife Sciences, Auburn University, Auburn, Alabama 36849, USA 4Present address: Department of Biological Sciences, North Dakota State University, Fargo, North Dakota 58105, USA ABSTRACT: Coastal habitats are susceptible to changes in the environment associated with alter- ations in salinity. A field study was conducted on natural populations of the sailfin molly Poecilia latipinna, the western mosquitofish Gambusia affinis and the least killifish Heterandria formosa col- lected from coastal marsh sites along a salinity gradient, to investigate the influence of salinity on body condition and reproductive life history traits. In brackish marsh sites male P. latipinna had the best body conditions, while females had similar body conditions across all 3 marsh types. Female P. latipinna had greater reproductive allotment and fecundity in brackish marshes, where this fish was most abundant. Specimens of G. affinis collected from fresh marsh sites had less favorable body condition, and females had lower reproductive allotment and fecundity than those collected from higher salinities. While G. affinis was more abundant in freshwater marshes than in higher salinity marshes, this higher abundance did not correspond with a better body condition or higher reproduc- tive effort, suggesting that G. -
Heterandria Formosa
Faculty of Life Sciences Albrecht Daniel Thaer-Institute of Agricultural and Horticultural Sciences Food-dependent development of behavioural types in Heterandria formosa M.Sc. thesis in the study program: Fishery Science and Aquaculture submitted by: Theis, Sebastian 1st Examiner (Supervisor): Prof. Dr. Arlinghaus, Robert Division of or Institution: Human dimensions and bio-economics of recreational fisheries, inter- and transdisciplinary fisheries research, fish and fisher behavioural ecology. Leibniz-Institute of Freshwater Ecology and Inland Fisheries (IGB) Humboldt-Universität zu Berlin (HU) 2nd Examiner: Dr. Schröder, Arne Division of or Institution: The ecological consequences of the joint individual variation in size-specific life histories and behavioural types. Leibniz-Institute of Freshwater Ecology and Inland Fisheries (IGB) Humboldt-Universität zu Berlin (HU) Berlin, June 23, 2017 i Content List of Figures ..................................................................................................................................... iii List of Tables ....................................................................................................................................... iv List of Abbreviations ........................................................................................................................... vi List of Utilized software ...................................................................................................................... vi Abstract .............................................................................................................................................. -
Fundulus Nottii, a Starhead Topminnow
5 American Currents Vol. 42, No. 1 FUNDULUS NOTTII, A STARHEAD TOPMINNOW Charles Nunziata Within the subgenus Zygonectes of the genus Fundulus, there main identification factors. The body pattern differences are is a super species group known as the “Starhead Topmin- well summarized in Page and Burr (2011). nows,” which includes Fundulus blairae (Western Starhead They are all excellent pond species suitable to the south- Topminnow); F. dispar (Starhead Topminnow); F. escambiae ern regions of the US that do not experience hard freezes or (Russetfin Topminnow); F. lineolatus (Lined Topminnow); prolonged periods below 40ºF. Natural populations tend to and F. nottii (Bayou Topminnow). According to Ghedotti be seasonal, breeding outdoors between late spring and late and Grose (1997), this super species group has been con- summer. One can expect pond populations to continue over firmed through a molecular biology analysis. many generations. The subgenus Zygonectes includes a number of other Because the starheads are not flashy, they were never Fundulus species, some similar to the starheads, and some popular in the killifish hobby. They have an elegant look significantly different in color and size. The other members of Zygonectes are F. chrysotus, cingulatus, euryzonus, luciae, notatus, olivaceus, and rubrifrons. Among these, F. luciae, a brackish water fish that inhabits an enormous coastal Atlan- tic range, is the most divergent from the others. There are a few distinctive markings shared by all the starhead topminnows: a dark blue to black bar under each eye, suggesting a teardrop pattern; a large well-defined gold spot on the top of the head; and a small gold dot at the dorsal fin insert.