A Field Guide to Fish Invaders of the Great Lakes Region
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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 -
Labidesthes Sicculus
Version 2, 2015 United States Fish and Wildlife Service Lower Great Lakes Fish and Wildlife Conservation Office 1 Atherinidae Atherinidae Sand Smelt Distinguishing Features: — (Atherina boyeri) — Sand Smelt (Non-native) Old World Silversides Old World Silversides Old World (Atherina boyeri) Two widely separated dorsal fins Eye wider than Silver color snout length 39-49 lateral line scales 2 anal spines, 13-15.5 rays Rainbow Smelt (Non -Native) (Osmerus mordax) No dorsal spines Pale green dorsally Single dorsal with adipose fin Coloring: Silver Elongated, pointed snout No anal spines Size: Length: up to 145mm SL Pink/purple/blue iridescence on sides Distinguishing Features: Dorsal spines (total): 7-10 Brook Silverside (Native) 1 spine, 10-11 rays Dorsal soft rays (total): 8-16 (Labidesthes sicculus) 4 spines Anal spines: 2 Anal soft rays: 13-15.5 Eye diameter wider than snout length Habitat: Pelagic in lakes, slow or still waters Similar Species: Rainbow Smelt (Osmerus mordax), 75-80 lateral line scales Brook Silverside (Labidesthes sicculus) Elongated anal fin Images are not to scale 2 3 Centrarchidae Centrarchidae Redear Sunfish Distinguishing Features: (Lepomis microlophus) Redear Sunfish (Non-native) — — Sunfishes (Lepomis microlophus) Sunfishes Red on opercular flap No iridescent lines on cheek Long, pointed pectoral fins Bluegill (Native) Dark blotch at base (Lepomis macrochirus) of dorsal fin No red on opercular flap Coloring: Brownish-green to gray Blue-purple iridescence on cheek Bright red outer margin on opercular flap -
Esox Lucius) Ecological Risk Screening Summary
Northern Pike (Esox lucius) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, February 2019 Web Version, 8/26/2019 Photo: Ryan Hagerty/USFWS. Public Domain – Government Work. Available: https://digitalmedia.fws.gov/digital/collection/natdiglib/id/26990/rec/22. (February 1, 2019). 1 Native Range and Status in the United States Native Range From Froese and Pauly (2019a): “Circumpolar in fresh water. North America: Atlantic, Arctic, Pacific, Great Lakes, and Mississippi River basins from Labrador to Alaska and south to Pennsylvania and Nebraska, USA [Page and Burr 2011]. Eurasia: Caspian, Black, Baltic, White, Barents, Arctic, North and Aral Seas and Atlantic basins, southwest to Adour drainage; Mediterranean basin in Rhône drainage and northern Italy. Widely distributed in central Asia and Siberia easward [sic] to Anadyr drainage (Bering Sea basin). Historically absent from Iberian Peninsula, Mediterranean France, central Italy, southern and western Greece, eastern Adriatic basin, Iceland, western Norway and northern Scotland.” Froese and Pauly (2019a) list Esox lucius as native in Armenia, Azerbaijan, China, Georgia, Iran, Kazakhstan, Mongolia, Turkey, Turkmenistan, Uzbekistan, Albania, Austria, Belgium, Bosnia Herzegovina, Bulgaria, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Macedonia, Moldova, Monaco, 1 Netherlands, Norway, Poland, Romania, Russia, Serbia, Slovakia, Slovenia, Sweden, Switzerland, United Kingdom, Ukraine, Canada, and the United States (including Alaska). From Froese and Pauly (2019a): “Occurs in Erqishi river and Ulungur lake [in China].” “Known from the Selenge drainage [in Mongolia] [Kottelat 2006].” “[In Turkey:] Known from the European Black Sea watersheds, Anatolian Black Sea watersheds, Central and Western Anatolian lake watersheds, and Gulf watersheds (Firat Nehri, Dicle Nehri). -
Ruffe (Gymnocephalus Cernua) Ecological Risk Screening Summary
U.S. Fish and Wildlife Service Ruffe (Gymnocephalus cernua) Ecological Risk Screening Summary US Fish and Wildlife Service, February 2011 Revised, July 2014 Revised, June 2015 Photo: USFWS 1 Native Range, and Status in the United States Native Range From Fuller et al. (2014): “Northern Europe and Asia (Berg 1949; Holcik and Hensel 1974; Wheeler 1978; Page and Burr 1991).” Status in the United States From Fuller et al. (2014): “The ruffe was first identified by Wisconsin DNR in specimens collected from the St. Louis River at the border of Minnesota and Wisconsin in 1987 (Pratt 1988; Pratt et al. 1992; Czypinski et al. 1999, 2000, 2001, 2003). Following that report, reexamination of archived samples revealed misidentified larval specimens of ruffe had been collected from the same area in 1986 (Pratt 1988). The ruffe subsequently spread into Duluth Harbor in Lake Superior and several tributaries of the lake (Underhill 1989; Czypinski et al. 1999, 2000, 2004; Scheidegger, pers. comm.; J. Slade, pers. comm.). It is found in the Amnicon, Flag, Iron, Middle, Raspberry, and Bad rivers, Chequamegon Bay, and Apostle Islands National Lakeshore in Wisconsin (Czypinski et al. 1999, 2000, 2001, 2003, 2004; Tilmant 1999). In August 1994, it was found in Saxon Harbor, Wisconsin, and in the upper peninsula of Michigan at the mouths of the Black and Ontonagon rivers (K. Kindt, pers. comm.). In the lower Peninsula of Michigan along Lake Huron, the first three specimens were caught at the mouth of the Thunder Bay River in August 1995 (K. Kindt, pers. comm.). This species has also been collected in Michigan in Lake Michigan, Lake Superior, Torch Lake, Little Bay de Noc in Escanaba, Big Bay de Noc, Misery River, Ontonagon River, Thunder Bay, and Sturgeon River Sloughs (Czypinski et al. -
Low-Head Dams Facilitate Round Goby Neogobius Melanostomus Invasion
Biol Invasions (2018) 20:757–776 https://doi.org/10.1007/s10530-017-1573-3 ORIGINAL PAPER Low-head dams facilitate Round Goby Neogobius melanostomus invasion Dustin Raab . Nicholas E. Mandrak . Anthony Ricciardi Received: 9 July 2017 / Accepted: 23 September 2017 / Published online: 3 October 2017 Ó Springer International Publishing AG 2017 Abstract Round Goby Neogobius melanostomus inclusion of both reservoir-associated abiotic variables invasion of the Grand River (Ontario, Canada) and Round Goby abundance as model terms. To presents an opportunity to assess the role of abiotic determine establishment potential of the uninvaded gradients in mediating the establishment and impact of reach immediately upstream, four environmental nonnative benthic fishes in rivers. In this system, habitat characteristics were used in discriminant sequential low-head dams delineate uninvaded and function analysis (DFA) to predict three potential invaded river reaches and create upstream gradients of outcomes of introduction: non-invaded and either increasing water velocity. We hypothesized that flow lower or higher Round Goby abundance (low and high refugia created by impounded reservoirs above low- invasion status, respectively) than the median number head dams enhance local Round Goby abundance. of Round Goby at invaded sites. Our DFA function Round Goby influence on the native fish community correctly classified non-invaded and high-abundance was determined by variance partitioning, and we used invasion status sites [ 85% of the time, with lower generalized additive models to identify small-bodied (73%) success in classifying low-abundance invasion benthic fish species most likely to be impacted by status sites, and the spatial pattern of our results Round Goby invasion. -
A Synopsis of the Biology and Life History of Ruffe
J. Great Lakes Res. 24(2): 170-1 85 Internat. Assoc. Great Lakes Res., 1998 A Synopsis of the Biology and Life History of Ruffe Derek H. Ogle* Northland College Mathematics Department Ashland, Wisconsin 54806 ABSTRACT. The ruffe (Gymnocephalus cernuus), a Percid native to Europe and Asia, has recently been introduced in North America and new areas of Europe. A synopsis of the biology and life history of ruffe suggests a great deal of variability exists in these traits. Morphological characters vary across large geographical scales, within certain water bodies, and between sexes. Ruffe can tolerate a wide variety of conditions including fresh and brackish waters, lacustrine and lotic systems, depths of 0.25 to 85 m, montane and submontane areas, and oligotrophic to eutrophic waters. Age and size at maturity dif- fer according to temperature and levels of mortality. Ruffe spawn on a variety ofsubstrates, for extended periods of time. In some populations, individual ruffe may spawn more than once per year. Growth of ruffe is affected by sex, morphotype, water type, intraspecific density, and food supply. Ruffe feed on a wide variety of foods, although adult ruffe feed predominantly on chironomid larvae. Interactions (i.e., competition and predation) with other species appear to vary considerably between system. INDEX WORDS: Ruffe, review, taxonomy, reproduction, diet, parasite, predation. INTRODUCTION DISTRIBUTION This is a review of the existing literature on Ruffe are native to all of Europe except for along ruffe, providing a synopsis of its biology and life the Mediterranean Sea, western France, Spain, Por- history. A review of the existing literature is tugal, Norway, northern Finland, Ireland, and Scot- needed at this time because the ruffe, which is na- land (Collette and Banarescu 1977, Lelek 1987). -
Proceedings of the Indiana Academy of Science
Ecology of the Southernmost Sympatric Population of the Brook Stickleback, Culaea inconstans, and the Ninespine Stickleback, Pungitius pungitius, in Crooked Lake, Indiana 1 - 3 Joseph S. Nelson, Indiana University Abstract The southernmost locality where Culaea inconstans, the brook stickle- back, and Pungitius pungitius, the ninespine stickleback, occur in sympatry is Crooked Lake, Indiana. Both species were first found in Crooked Lake in 1966 with rotenone, gillnets, and Plexiglas traps. Culaea and Pungitius occur between Zy2 and 10 m and 5 and 3 m, respectively. The summer range in pH for the two species is 7.6 to 8.6 and 7.4 to 8.6, respectively. The temperature range is between 12 and 24 and 6 and 24, respectively. Both sticklebacks probably spawn in rooted aquatics. Pungitius adults, however, generally occur below the zone of rooted aquatics. Fully ripe eggs were found in the limited number of Culaea adults between June 26 and July 19. Pimgitius with fully ripe eggs were found from April to August. Identifiable young of Culaea and Pungitius, 12 mm standard length, were first collected July 19 and June 15, respectively. The largest Culaea was 38 mm while the largest Pungitius was 59 mm standard length. Culaea was found in the stomachs of Micropterus salmoides and Perca flavescens. Stomachs of the latter two species and of Esox americanus contained Pungitius. Introduction Culaea (—Eucalia) inconstans (Kirtland), the brook stickleback, occurs in lakes, ponds, and streams across northern North America from northeastern British Columbia to New Brunswick and south to Indiana. Pungitius pungitius (Linnaeus), the ninespine stickleback, oc- curs in the freshwaters and along the coastlines of northern Asia, Europe, and northern North America. -
Eurasian Ruffe (Gymnocephalus Cernua), Native to Northern Europe and Asia, Have Threatened the Great Lakes and Surrounding States Since the Late 1980S
State of Michigan’s Status and Strategy for Eurasian Ruffe Management Scope Invasive Eurasian ruffe (Gymnocephalus cernua), native to northern Europe and Asia, have threatened the Great Lakes and surrounding states since the late 1980s. The goals of this document are to: • Summarize the current understanding level of the biology and ecology of Eurasian ruffe. • Summarize the current management options for Eurasian ruffe in Michigan. • Identify possible future directions of Eurasian ruffe management in Michigan. Biology and Ecology I. Identification Eurasian ruffe, also known as blacktail Gary Cholwek – National Biological Service or river ruffe, is a member of genus Gymnocephalus within Percidae. Eurasian ruffe is a small, aggressive, benthic fish native to Europe and Asia. The species resemble yellow perch with distinct walleye markings (McLean 1997). The Eurasian ruffe can be distinguished from other perch by their large, jointed dorsal fin composed of 11 to 16 spines with rows of dark spots between each spine. Adult ruffe are typically five to six inches long with large individuals rarely exceeding 10 inches. They have a small, downturned mouth, lack scales on their head, and are slimy when handled (McLean 1997). Eurasian ruffe have two dorsal fins, one spiny (anterior) and one soft (posterior), and are commonly mistaken for troutperch, which have only a single dorsal fin. Their coloration consists of an olive-brown dorsal surface, pale sides, and a yellow underside (Fuller 2014, Hajjar 2002). Eurasian ruffe have two ventral fins with sharp spines on the leading edges; the anterior fin has only one spine where the posterior fin has two spines. -
Minnesota Fishes: Just How Many Species Are There Anyway?
B Spring 2015 American Currents 10 MINNESOTA FISHES: JUST HOW MANY SPECIES ARE THERE ANYWAY? Jay Hatch Dept. of Postsecondary Teaching and Learning and James Ford Bell Museum of Natural History, University of Minnesota INTRODUCTION FIGURING OUT THE COUNT In terms of fish diversity, for a state at the northern edge and Were they ever really here? halfway between the east–west extremes of the contiguous On the surface, this one appears pretty simple, but it can USA, Minnesota doesn’t do badly. Of the five states and two cause way more gray hairs than you might think. For ex- Canadian provinces bordering it, only Wisconsin boasts as ample, what do you do if Minnesota’s ichthyological fore- many or more species. We (my fish biology colleagues and )I fathers—like Albert Woolman and Ulysses Cox—reported believe this is true, but counting species is not quite as easy species such as the Chestnut Lamprey (Icthyomyzon casta- as it seems. You’re asking: What could be easier? Just find out neus) from the Minnesota River basin or the Longnose Gar if a fish species swims in your lakes or streams, then count it, (Lepisosteus osseus) from the Red River of the North basin right? Well, as they used to say in the Hertz rental car com- (see Figure 1 for Minnesota’s 10 major basins), but no one mercial, “not exactly.” else has ever collected these species in those basins over the What kinds of issues lead to “not exactly?” Quite a few, last 120 years? Look at the specimens, right? Good luck; including the uncertainty of old or historical records, the they no longer exist. -
Caviar, Soup and Other Dishes Made of Eurasian Ruffe, Gymnocephalus
Svanberg and Locker Journal of Ethnic Foods (2020) 7:3 Journal of Ethnic Foods https://doi.org/10.1186/s42779-019-0042-2 ORIGINAL ARTICLE Open Access Caviar, soup and other dishes made of Eurasian ruffe, Gymnocephalus cernua (Linnaeus, 1758): forgotten foodstuff in central, north and west Europe and its possible revival Ingvar Svanberg1* and Alison Locker2 Abstract Background: Many freshwater fish species that were earlier appreciated by consumers have disappeared in the central, north and west European foodways. Although they were regarded as healthy and tasty, commercially captured marine species and highly processed products have nowadays replaced these fishes. The global transformations of the food system contribute to the erosion of many local foodstuffs. Habitual tastes disappear. Methods: The article is based on a vast amount of scattered original data found in sources such as in local ethnographical studies, fishing reports, topographic literature, zoological literature, archaeological fish reports, and cookery books Results and discussion: This article discusses how Eurasian ruffe, Gymnocephalus cernua (L., 1758), once was used, and the reason for its disappearance, as foodstuff in some parts of Europe. Actually, it is a fish with potential for a revival as fine food. The authors discuss the chances of its rediscovery as a foodstuff, which could be used for instance within the concept of the New Nordic Cuisine and beyond. There are also environmental reasons to increase the use of local biodiversity not to mention making tastier -
Reproductive Cycle and the Related Spatial and Temporal Distribution Of
Reproductive cycle and OCEANOLOGIA, 44 (4), 2002. pp. 475–490. the related spatial and 2002, by Institute of temporal distribution of Oceanology PAS. the ninespine stickleback KEYWORDS (P ungitius pungitius L.) Ninespine stickleback in Puck Bay Breeding period Spawning Stages of maturity Puck Bay Ewa Sokołowska Institute of Oceanology, Polish Academy of Sciences, Powstańców Warszawy 55, PL–81–712 Sopot, Poland; e-mail: [email protected] Krzysztof E. Skóra Marine Station, Institute of Oceanography, University of Gdańsk, Morska 2, PL–84–150 Hel, Poland; e-mail: [email protected] Manuscript received 3 July 2002, reviewed 23 October 2002, accepted 28 October 2002. Abstract The cycle of gonad development and related changes in the length structure and spatial-temporal distribution of ninespine sticklebacks (Pungitius pungitius L.) in Puck Bay were studied. Observations were carried out in the shallow shore zones, as well as in the deeper epipelagic zone of the Bay. Ninespine sticklebacks reproduce in the brackish environment of Puck Bay, breeding in its warmer, inshore zones. Reproduction takes place in the spring and summer months, from April to July. One female spawns several clutches of eggs during one breeding season. The average length of ninespine sticklebacks in Puck Bay was about 40 mm, and the sex ratio in the population was close to 1:1. However, both length structure and sex ratio were subject to local and periodic variations, resulting from possible breeding-related territorial divisions. Higher gonadosomatic indices in females in early spring represented the transition of fish to the advanced vitelligenous phase. The lowest GSI of males during the breeding season indicated the termination of spermatogenesis. -
Baitfish Primer
2018 THE BAITFISH PRIMER A GUIDE TO IDENTIFYING AND PROTECTING ONTARIO'S BAITFISHES 2018 Version Produced by Fisheries and Oceans Canada Burlington, ON Ontario Ministry of Natural Resources and Forestry Peterborough, ON Bait Association of Ontario Peterborough, ON and The Ontario Federation of Anglers and Hunters Peterborough, ON Published by: Communications Branch Fisheries and Oceans Canada Burlington, Ontario L7S 1A1 DFO/2018-2000 (c) Her Majesty the Queen in Right of Canada 2018 Catalogue number: Fs134-7/2018E ISBN: 978-0-660-20453-6 Catalogue number for PDF: Fs134-7/2018E-PDF ISBN: 978-0-660-20452-9 Printed on recycled paper. This publication is available upon request in multiple formats by contacting Fisheries and Oceans Canada at [email protected] or (613) 993-0999. Cette publication est aussi disponible en français. THE BAITFISH PRIMER by Becky Cudmore and Nicholas E. Mandrak TABLE OF CONTENTS PAGE 4 INTRODUCTION PAGE 6 ACKNOWLEDGEMENTS PAGE 7 SUMMARY OF LEGISLATION & REGULATIONS RELATED TO BAITFISHES PAGE 9 POTENTIAL IMPACTS OF HARVEST AND USE OF BAITFISHES PAGE 11 BAITFISH HABITAT PAGE 12 ANATOMICAL KEY PAGE 13 PICTORIAL KEY OF FISH FAMILIES IN ONTARIO PAGE 16 SPECIES ACCOUNTS PAGE 38 WHAT YOU CAN DO TO MINIMIZE IMPACTS TO AQUATIC ECOSYSTEMS PAGE 39 FURTHER READING PAGE 39 CONTACTS 3 THE BAITFISH PRIMER INTRODUCTION Recreational angling is a popular pastime in lead to further declines and possible Ontario - well over one million residents extinction. Even within fish families and visitors enjoy angling every year. generally considered legal baitfishes, there Angling supports many aspects of the are individual fish species that cannot be Ontario economy, including the baitfish used.