Life History and Status of Alligator Gar Atractosteus Spatula, with Recommendations for Management
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Fish Inventory at Stones River National Battlefield
Fish Inventory at Stones River National Battlefield Submitted to: Department of the Interior National Park Service Cumberland Piedmont Network By Dennis Mullen Professor of Biology Department of Biology Middle Tennessee State University Murfreesboro, TN 37132 September 2006 Striped Shiner (Luxilus chrysocephalus) – nuptial male From Lytle Creek at Fortress Rosecrans Photograph by D. Mullen Table of Contents List of Tables……………………………………………………………………….iii List of Figures………………………………………………………………………iv List of Appendices…………………………………………………………………..v Executive Summary…………………………………………………………………1 Introduction…………………………………………………………………...……..2 Methods……………………………………………………………………………...3 Results……………………………………………………………………………….7 Discussion………………………………………………………………………….10 Conclusions………………………………………………………………………...14 Literature Cited…………………………………………………………………….15 ii List of Tables Table1: Location and physical characteristics (during September 2006, and only for the riverine sites) of sample sites for the STRI fish inventory………………………………17 Table 2: Biotic Integrity classes used in assessing fish communities along with general descriptions of their attributes (Karr et al. 1986) ………………………………………18 Table 3: List of fishes potentially occurring in aquatic habitats in and around Stones River National Battlefield………………………………………………………………..19 Table 4: Fish species list (by site) of aquatic habitats at STRI (October 2004 – August 2006). MF = McFadden’s Ford, KP = King Pond, RB = Redoubt Brannan, UP = Unnamed Pond at Redoubt Brannan, LC = Lytle Creek at Fortress Rosecrans……...….22 Table 5: Fish Species Richness estimates for the 3 riverine reaches of STRI and a composite estimate for STRI as a whole…………………………………………………24 Table 6: Index of Biotic Integrity (IBI) scores for three stream reaches at Stones River National Battlefield during August 2005………………………………………………...25 Table 7: Temperature and water chemistry of four of the STRI sample sites for each sampling date…………………………………………………………………………….26 Table 8 : Total length estimates of specific habitat types at each riverine sample site. -
Tennessee Fish Species
The Angler’s Guide To TennesseeIncluding Aquatic Nuisance SpeciesFish Published by the Tennessee Wildlife Resources Agency Cover photograph Paul Shaw Graphics Designer Raleigh Holtam Thanks to the TWRA Fisheries Staff for their review and contributions to this publication. Special thanks to those that provided pictures for use in this publication. Partial funding of this publication was provided by a grant from the United States Fish & Wildlife Service through the Aquatic Nuisance Species Task Force. Tennessee Wildlife Resources Agency Authorization No. 328898, 58,500 copies, January, 2012. This public document was promulgated at a cost of $.42 per copy. Equal opportunity to participate in and benefit from programs of the Tennessee Wildlife Resources Agency is available to all persons without regard to their race, color, national origin, sex, age, dis- ability, or military service. TWRA is also an equal opportunity/equal access employer. Questions should be directed to TWRA, Human Resources Office, P.O. Box 40747, Nashville, TN 37204, (615) 781-6594 (TDD 781-6691), or to the U.S. Fish and Wildlife Service, Office for Human Resources, 4401 N. Fairfax Dr., Arlington, VA 22203. Contents Introduction ...............................................................................1 About Fish ..................................................................................2 Black Bass ...................................................................................3 Crappie ........................................................................................7 -
A Middle Triassic Kyphosichthyiform from Yunnan, China, and Phylogenetic Reassessment of Early Ginglymodians
SUPPLEMENTARY DATA A Middle Triassic kyphosichthyiform from Yunnan, China, and phylogenetic reassessment of early ginglymodians XU Guang-Hui1,2 MA Xin-Ying1,2,3 WU Fei-Xiang1,2 REN Yi1,2,3 (1 Key Laboratory of Vertebrate Evolution and Human Origins of Chinese Academy of Sciences, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences Beijing 100044 [email protected]) (2 CAS Center for Excellence in Life and Paleoenvironment Beijing 100044) (3 University of Chinese Academy of Sciences Beijing 100049) Part A Material examined and references Amia calva and Solnhofenamia elongata (Grande and Bemis, 1998); Araripelepidotes temnurus (Maisey, 1991; Thies, 1996); Asialepidotus shingyiensis (Xu and Ma, 2018); Atractosteus spatula, Cuneatus wileyi, Dentilepisosteus laevis, Lepisosteus osseus, Masillosteus janeae, and Obaichthys decoratus (Grande, 2010); Caturus furcatus (Patterson, 1975; Lambers, 1992; Grande and Bemis, 1998; FMNH UC2057); Dorsetichthys (‘Pholidophorus’) bechei (Patterson, 1975; Grande and Bemis, 1998; Arratia, 2013); Elops hawaiensis (Forey, 1973); Fuyuanichthys wangi (Xu et al., 2018); Ichthyokentema purbeckensis (Griffith and Patterson, 1963); Ionoscopus cyprinoides (Grande and Bemis, 1998; Maisey, 1999; FMNH P15472); Isanichthys palustris (Cavin and Suteethorn, 2006); Kyphosichthys grandei (Xu and Wu, 2012; Sun and Ni, 2018); Lashanichthys (‘Sangiorgioichthys’) sui (López-Arbarello et al., 2011); Lashanichthys (‘Sangiorgioichthys’) yangjuanensis (Chen et al, 2014); Lepidotes gigas (Thies, -
Spatial Criteria Used in IUCN Assessment Overestimate Area of Occupancy for Freshwater Taxa
Spatial Criteria Used in IUCN Assessment Overestimate Area of Occupancy for Freshwater Taxa By Jun Cheng A thesis submitted in conformity with the requirements for the degree of Masters of Science Ecology and Evolutionary Biology University of Toronto © Copyright Jun Cheng 2013 Spatial Criteria Used in IUCN Assessment Overestimate Area of Occupancy for Freshwater Taxa Jun Cheng Masters of Science Ecology and Evolutionary Biology University of Toronto 2013 Abstract Area of Occupancy (AO) is a frequently used indicator to assess and inform designation of conservation status to wildlife species by the International Union for Conservation of Nature (IUCN). The applicability of the current grid-based AO measurement on freshwater organisms has been questioned due to the restricted dimensionality of freshwater habitats. I investigated the extent to which AO influenced conservation status for freshwater taxa at a national level in Canada. I then used distribution data of 20 imperiled freshwater fish species of southwestern Ontario to (1) demonstrate biases produced by grid-based AO and (2) develop a biologically relevant AO index. My results showed grid-based AOs were sensitive to spatial scale, grid cell positioning, and number of records, and were subject to inconsistent decision making. Use of the biologically relevant AO changed conservation status for four freshwater fish species and may have important implications on the subsequent conservation practices. ii Acknowledgments I would like to thank many people who have supported and helped me with the production of this Master’s thesis. First is to my supervisor, Dr. Donald Jackson, who was the person that inspired me to study aquatic ecology and conservation biology in the first place, despite my background in environmental toxicology. -
Gar (Lepisosteidae)
Indiana Division of Fish and Wildlife’s Animal Information Series Gar (Lepisosteidae) Gar species found in Indiana waters: -Longnose Gar (Lepisosteus osseus) -Shortnose Gar (Lepisosteus platostomus) -Spotted Gar (Lepisosteus oculatus) -Alligator Gar* (Atractosteus spatula) *Alligator Gar (Atractosteus spatula) Alligator gar were extirpated in many states due to habitat destruction, but now they have been reintroduced to their old native habitat in the states of Illinois, Missouri, Arkansas, and Kentucky. Because they have been stocked into the Ohio River, there is a possibility that alligator gar are either already in Indiana or will be found here in the future. Alligator gar are one of the largest freshwater fishes of North America and can reach up to 10 feet long and weigh 300 pounds. Alligator gar are passive, solitary fishes that live in large rivers, swamps, bayous, and lakes. They have a short, wide snout and a double row of teeth on the upper jaw. They are ambush predators that eat mainly fish but have also been seen to eat waterfowl. They are not, however, harmful to humans, as they will only attack an animal that they can swallow whole. Photo Credit: Duane Raver, USFWS Other Names -garpike, billy gar -Shortnose gar: shortbill gar, stubnose gar -Longnose gar: needlenose gar, billfish Why are they called gar? The Anglo-Saxon word gar means spear, which describes the fishes’ long spear-like appearance. The genus name Lepisosteus contains the Greek words lepis which means “scale” and osteon which means “bone.” What do they look like? Gar are slender, cylindrical fishes with hard, diamond-shaped and non-overlapping scales. -
The Feeding Habits and Relative Abundances of Bowfin, Spotted Gar, and Largemouth Bass: Can Native Piscivores Control Invasive Common Carp?
INHS Reports SEPTEMBER 2014 • NO. 412(3) The Feeding Habits and Relative Abundances of Bowfin, Spotted Gar, and Largemouth Bass: Can Native Piscivores Control Invasive Common Carp? The Illinois River is a very productive, health of the Illinois River and other near Hennepin, Illinois experienced floodplain river system; however, its nat- rivers worldwide. Thompson and Flag Common Carp survival after a rotenone ural biological productivity has changed lakes at The Nature Conservancy’s (TNC) application to eradicate them during the through floodplain disconnection, excess Emiquon Preserve serve as one example initial restoration. Due to rapid population nutrient loading, and invasive fish species and have experienced increased Com- growth of Common Carp, Hennepin and introductions. As just one example, Com- mon Carp relative abundances since Hopper lakes experienced major declines mon Carp (Cyprinus carpio) directly and restoration. Management of Common in aquatic macrophyte densities and indirectly degrade aquatic ecosystems Carp is critical for maintaining healthy waterfowl use shortly after restoration. through benthic foraging behaviors. aquatic ecosystems and piscicides, such In addition to a rotenone treatment, as rotenone, are not 100% effective. For biomanipulation of the Largemouth Bass Currently, floodplain restoration efforts example, a floodplain restoration project (Micropterus salmoides) population has are intended to improve the natural known as Hennepin and Hopper Lakes been tested at the Emiquon Preserve and results suggested -
Ecology of the Alligator Gar, Atractosteusspatula, in the Vicente G1;Jerreroreservoir, Tamaulipas, Mexico
THE SOUTHWESTERNNATURALIST 46(2):151-157 JUNE 2001 ECOLOGY OF THE ALLIGATOR GAR, ATRACTOSTEUSSPATULA, IN THE VICENTE G1;JERRERORESERVOIR, TAMAULIPAS, MEXICO .-., FRANCISCO J. GARCiA DE LEON, LEONARDO GoNzALEZ-GARCiA, JOSE M. HERRERA-CAsTILLO, KIRK O. WINEMILLER,* AND ALFONSO BANDA-VALDES Laboratorio de Biologia lntegrativa, lnstituto Tecnol6gicode Ciudad Victoria, Boulevard Emilio Fortes Gil1301, Ciudad Victoria, CP 87010, Tamaulipas, Mexico (F]GL, LGG,]MHC) Department of Wildlife and FisheriesSciences, Texas A&M University, CollegeStation, TX 77843-2258 (KO~ Direcci6n Generalde Pescadel Gobiernodel Estado de Tamaulipas, Ciudad Victoria, Tamaulipas, Mexico (ABV) * Correspondent:[email protected] ABsTRACf-We provide the first ecological account of the alligator gar, Atractosteusspatula, in the Vicente Guerrero Reservoir, Tamaulipas, Mexico. During March to September, 1998, the local fishery cooperative captured more than 23,000 kg of alligator gar from the reservoir. A random sample of their catch was dominated by males, which were significantly smaller than females. Males and females had similar weight-length relationships. Relative testicular weight varied little season- ally, but relative ovarian weight showed a strong seasonal pattern that indicated peak spawning activity during July and August. Body condition of both sexes also varied in a pattern consistent with late summer spawning. Fishing for alligator gar virtually ceased from October to February, when nonreproductive individuals were presumed to move offshore to deeper water. Alligator gar fed primarily on largemouth bass, Micropterus salmoides,and less frequently on other fishes. The gillnet fishery for alligator gar in the reservoir appears to be based primarily on individuals that move into shallow, shoreline areas to spawn. Males probably remain in these habitats longer than females. -
Species Composition and Invasion Risks of Alien Ornamental Freshwater
www.nature.com/scientificreports OPEN Species composition and invasion risks of alien ornamental freshwater fshes from pet stores in Klang Valley, Malaysia Abdulwakil Olawale Saba1,2, Ahmad Ismail1, Syaizwan Zahmir Zulkifi1, Muhammad Rasul Abdullah Halim3, Noor Azrizal Abdul Wahid4 & Mohammad Noor Azmai Amal1* The ornamental fsh trade has been considered as one of the most important routes of invasive alien fsh introduction into native freshwater ecosystems. Therefore, the species composition and invasion risks of fsh species from 60 freshwater fsh pet stores in Klang Valley, Malaysia were studied. A checklist of taxa belonging to 18 orders, 53 families, and 251 species of alien fshes was documented. Fish Invasiveness Screening Test (FIST) showed that seven (30.43%), eight (34.78%) and eight (34.78%) species were considered to be high, medium and low invasion risks, respectively. After the calibration of the Fish Invasiveness Screening Kit (FISK) v2 using the Receiver Operating Characteristics, a threshold value of 17 for distinguishing between invasive and non-invasive fshes was identifed. As a result, nine species (39.13%) were of high invasion risk. In this study, we found that non-native fshes dominated (85.66%) the freshwater ornamental trade in Klang Valley, while FISK is a more robust tool in assessing the risk of invasion, and for the most part, its outcome was commensurate with FIST. This study, for the frst time, revealed the number of high-risk ornamental fsh species that give an awareness of possible future invasion if unmonitored in Klang Valley, Malaysia. As a global hobby, fshkeeping is cherished by both young and old people. -
Systematic Morphology of Fishes in the Early 21St Century
Copeia 103, No. 4, 2015, 858–873 When Tradition Meets Technology: Systematic Morphology of Fishes in the Early 21st Century Eric J. Hilton1, Nalani K. Schnell2, and Peter Konstantinidis1 Many of the primary groups of fishes currently recognized have been established through an iterative process of anatomical study and comparison of fishes that has spanned a time period approaching 500 years. In this paper we give a brief history of the systematic morphology of fishes, focusing on some of the individuals and their works from which we derive our own inspiration. We further discuss what is possible at this point in history in the anatomical study of fishes and speculate on the future of morphology used in the systematics of fishes. Beyond the collection of facts about the anatomy of fishes, morphology remains extremely relevant in the age of molecular data for at least three broad reasons: 1) new techniques for the preparation of specimens allow new data sources to be broadly compared; 2) past morphological analyses, as well as new ideas about interrelationships of fishes (based on both morphological and molecular data) provide rich sources of hypotheses to test with new morphological investigations; and 3) the use of morphological data is not limited to understanding phylogeny and evolution of fishes, but rather is of broad utility to understanding the general biology (including phenotypic adaptation, evolution, ecology, and conservation biology) of fishes. Although in some ways morphology struggles to compete with the lure of molecular data for systematic research, we see the anatomical study of fishes entering into a new and exciting phase of its history because of recent technological and methodological innovations. -
Evolution of the Nitric Oxide Synthase Family in Vertebrates and Novel
bioRxiv preprint doi: https://doi.org/10.1101/2021.06.14.448362; this version posted June 14, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Evolution of the nitric oxide synthase family in vertebrates 2 and novel insights in gill development 3 4 Giovanni Annona1, Iori Sato2, Juan Pascual-Anaya3,†, Ingo Braasch4, Randal Voss5, 5 Jan Stundl6,7,8, Vladimir Soukup6, Shigeru Kuratani2,3, 6 John H. Postlethwait9, Salvatore D’Aniello1,* 7 8 1 Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, 80121, 9 Napoli, Italy 10 2 Laboratory for Evolutionary Morphology, RIKEN Center for Biosystems Dynamics 11 Research (BDR), Kobe, 650-0047, Japan 12 3 Evolutionary Morphology Laboratory, RIKEN Cluster for Pioneering Research (CPR), 2-2- 13 3 Minatojima-minami, Chuo-ku, Kobe, Hyogo, 650-0047, Japan 14 4 Department of Integrative Biology and Program in Ecology, Evolution & Behavior (EEB), 15 Michigan State University, East Lansing, MI 48824, USA 16 5 Department of Neuroscience, Spinal Cord and Brain Injury Research Center, and 17 Ambystoma Genetic Stock Center, University of Kentucky, Lexington, Kentucky, USA 18 6 Department of Zoology, Faculty of Science, Charles University in Prague, Prague, Czech 19 Republic 20 7 Division of Biology and Biological Engineering, California Institute of Technology, 21 Pasadena, CA, USA 22 8 South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, 23 Faculty of Fisheries and Protection of Waters, University of South Bohemia in Ceske 24 Budejovice, Vodnany, Czech Republic 25 9 Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA 26 † Present address: Department of Animal Biology, Faculty of Sciences, University of 27 Málaga; and Andalusian Centre for Nanomedicine and Biotechnology (BIONAND), 28 Málaga, Spain 29 30 * Correspondence: [email protected] 31 32 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.06.14.448362; this version posted June 14, 2021. -
Estimating Spawning Times of Alligator Gar (Atractosteus Spatula) in Lake Texoma, Oklahoma
46 Estimating Spawning Times of Alligator Gar (Atractosteus spatula) in Lake Texoma, Oklahoma Richard A. Snow Oklahoma Department of Wildlife Conservation, Oklahoma Fishery Research Laboratory, Norman, OK 73072 James M. Long U.S. Geological Survey Oklahoma Cooperative Fish and Wildlife Research Unit, Department of Natural Resource Ecology and Management, Oklahoma State University, Stillwater, OK 74078 Abstract: In 2013, juvenile Alligator Gar were sampled in the reservoir-river interface of the Red River arm of Lake Texoma. The Red River, which flows 860 km along Oklahoma’s border with Texas, is the primary in-flow source of Lake Texoma, and is impounded by Denison Dam. Mini- fyke nets were deployed using an adaptive random cluster sampling design, which has been used to effectively sample rare species. Lapilli otoliths (one of the three pair of ear stones found within the inner ear of fish) were removed from juvenile Alligator Gar collected in July of 2013. Daily ages were estimated by counting the number of rings present, and spawn dates were back-calculated from date of capture and subtracting 8 days (3 days from spawn to hatch and 5 days from hatch to swim- up when the first ring forms). Alligator Gar daily age estimation ranged from 50 to 63 days old since swim-up. Spawn dates corresponded to rising pool elevations of Lake Texoma and water pulses of tributaries. ©2015 Oklahoma Academy of Science Introduction In its native range, Alligator Gar spawns from early April through the middle of June The Alligator Gar (Atractosteus spatula) is in conjunction with seasonal flooding events the largest freshwater fish species in Oklahoma (Etnier and Starnes 1993, Ferrara 2001, Inebnit and the third largest in North America (Page and 2009). -
Fish I.D. Guide
mississippi department of wildlife, fisheries, and parks FRESHWATER FISHES COMMON TO MISSISSIPPI a fish identification guide MDWFP • 1505 EASTOVER DRIVE • JACKSON, MS 39211 • WWW.MDWFP.COM Table of Contents Contents Page Number • White Crappie . 4 • Black Crappie. 5 • Magnolia Crappie . 6 • Largemouth Bass. 7 • Spotted Bass . 8 • Smallmouth Bass. 9 • Redear. 10 • Bluegill . 11 • Warmouth . 12 • Green sunfish. 13 • Longear sunfish . 14 • White Bass . 15 • Striped Bass. 16 • Hybrid Striped Bass . 17 • Yellow Bass. 18 • Walleye . 19 • Pickerel . 20 • Channel Catfish . 21 • Blue Catfish. 22 • Flathead Catfish . 23 • Black Bullhead. 24 • Yellow Bullhead . 25 • Shortnose Gar . 26 • Spotted Gar. 27 • Longnose Gar . 28 • Alligator Gar. 29 • Paddlefish. 30 • Bowfin. 31 • Freshwater Drum . 32 • Common Carp. 33 • Bigmouth Buffalo . 34 • Smallmouth Buffalo. 35 • Gizzard Shad. 36 • Threadfin Shad. 37 • Shovelnose Sturgeon. 38 • American Eel. 39 • Grass Carp . 40 • Bighead Carp. 41 • Silver Carp . 42 White Crappie (Pomoxis annularis) Other Names including reservoirs, oxbow lakes, and rivers. Like other White perch, Sac-a-lait, Slab, and Papermouth. members of the sunfish family, white crappie are nest builders. They produce many eggs, which can cause Description overpopulation, slow growth, and small sizes in small White crappie are deep-bodied and silvery in color, lakes and ponds. White crappie spawn from March ranging from silvery-white on the belly to a silvery-green through May when water temperatures are between or dark green on the back with possible blue reflections. 58ºF and 65ºF. White crappie can tolerate muddier There are several dark vertical bars on the sides. Males water than black crappie. develop dark coloration on the throat and head during the spring spawning season, which can cause them to be State Record mistaken for black crappie.