Water Withdrawal and Ninespine Stickleback
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Evolution of Body Shape in Haida Gwaii Three-Spined Stickleback
Journal of Fish Biology (2007) 70, 1484–1503 doi:10.1111/j.1095-8649.2007.01425.x, available online at http://www.blackwell-synergy.com 10 000 years later: evolution of body shape in Haida Gwaii three-spined stickleback M. A. SPOLJARIC AND T. E. REIMCHEN* Department of Biology, University of Victoria, Victoria BC V8X 4A5, Canada (Received 29 April 2006, Accepted 23 December 2006) The body shape of 1303 adult male three-spined stickleback Gasterosteus aculeatus from 118 populations on Haida Gwaii archipelago off the mid-coast of British Columbia was investigated using discriminant function analysis on partial warp scores generated from 12 homologous landmarks on a digital image of each fish. Results demonstrated geographical differences in adult body shape that could be predicted by both abiotic and biotic factors of the habitat. Populations with derived shape (CV1À), including thick peduncles, posterior and closely spaced dorsal spines, anterior pelvis, small dorsal and anal fins, were found in small, shallow, stained ponds, and populations with less derived shape (CV1þ), with small narrow peduncles, anterior and widely spaced dorsal spines, posterior pelvis, large dorsal and anal fins were found in large, deep, clear lakes. This relationship was replicated between geographic regions; divergent mtDNA haplotypes in lowland populations; between predation regimes throughout the archipelago, and in each geographical region and between predation regimes in lowland populations monomorphic for the Euro and North American mtDNA haplotype. There were large-bodied populations with derived shape (CV2À), including small heads and shallow elongate bodies in open water habitats of low productivity, and populations with smaller size and less derived shape (CV2þ), with large heads and deeper bodies in higher productivity, structurally complex habitats. -
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 -
Teleostei, Syngnathidae)
ZooKeys 934: 141–156 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.934.50924 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae) Graham Short1,2,3, Louw Claassens4,5,6, Richard Smith4, Maarten De Brauwer7, Healy Hamilton4,8, Michael Stat9, David Harasti4,10 1 Research Associate, Ichthyology, Australian Museum Research Institute, Sydney, Australia 2 Ichthyology, California Academy of Sciences, San Francisco, USA 3 Ichthyology, Burke Museum, Seattle, USA 4 IUCN Seahorse, Pipefish Stickleback Specialist Group, University of British Columbia, Vancouver, Canada5 Rhodes University, Grahamstown, South Africa 6 Knysna Basin Project, Knysna, South Africa 7 University of Leeds, Leeds, UK 8 NatureServe, Arlington, Virginia, USA 9 University of Newcastle, Callaghan, NSW, Australia 10 Port Stephens Fisheries Institute, NSW, Australia Corresponding author: Graham Short ([email protected]) Academic editor: Nina Bogutskaya | Received 13 February 2020 | Accepted 12 April 2020 | Published 19 May 2020 http://zoobank.org/E9104D84-BB71-4533-BB7A-2DB3BD4E4B5E Citation: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141–156. https://doi.org/10.3897/zookeys.934.50924 Abstract A new species and the first confirmed record of a true pygmy seahorse from Africa,Hippocampus nalu sp. nov., is herein described on the basis of two specimens, 18.9–22 mm SL, collected from flat sandy coral reef at 14–17 meters depth from Sodwana Bay, South Africa. -
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). -
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. -
Wetland Wildlife Cards
Wetland wildlife cards • To make the cards, cut the line across the width of your paper then fold each half in half again so you end up with a picture on one side and the information on the other. Stick the two sides together with glue. Cut Fold Fold Stickleback Diet: Insects, crustaceans, tadpoles and smaller fish Wetland adaptations: Some sticklebacks have adapted to be able to cope with both fresh and saltwater meaning they can live in both rivers and the sea Classification: Vertebrate - Fish Habitat: Ponds, lakes, ditches and rivers Did you know? The male develops a bright red throat and belly and performs a courtship dance to attract a mate. The male also builds and protects the nest Cut Cut Eel Diet: Plants, dead animals, fish eggs, invertebrates and other fish Wetland adaptations: Long, narrow body enables it to get into crevices Classification: Vertebrate - Fish Habitat: Rivers and ditches Did you know? Adult eels migrate 3,000 miles (4,800 km) to the Sargasso Sea to spawn. It then takes the young eels two or three years to drift back to their homes here in the UK Fold Fold Smooth newt Diet: Insects, caterpillars, worms and slugs while on land; crustaceans, molluscs and tadpoles when in the water Wetland adaptations: Can breathe through their skin Classification: Vertebrate - Amphibian Habitat: Ponds in spring; woodland, grassland, hedgerows and marshes in summer and autumn; hibernates underground, among tree roots and under rocks and logs over winter Did you know? Their body gives out a poisonous fluid when they feel threatened -
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. -
The Adaptive Significance of Dorsal Spine Variation in the Fourspine Stickleback, Apeltes Quadracus
Heredity (1984),53(2), 383—396 1984. The Genetical Society of Great Britain THEADAPTIVE SIGNIFICANCE OF DORSAL SPINE VARIATION IN THE FOURSPINE STICKLEBACK, APELTES QUADRACUS. IV. PHENOTYPIC COVARIATION WITH CLOSELY RELATED SPECIES 0. M. BLOUW* AND 0. W. HAGEN Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B6EI Received2.xii.83 SUMMARY The fourspine stickleback (Apeltes quadracus) and ninespine stickleback (Pungitiuspungitius)have similar ecologies, they often coexist, and they share parallel polymorphisms for the number of dorsal spines. Spine number is posi- tively correlated between them for 86 sites in eastern Canada. Dorsal spine length is positively correlated with spine number within each species, and spine length is positively correlated between them. Spine length for both species is also positively correlated with the presence of predatory fishes and negatively corre- lated with vegetation cover. Finally, spine number for both Apeltes and Pungirius is lower where they coexist with a new species of stickleback (Gasterosteus sp.) which is found only in environments where predation risk is low. These patterns of covariation within and between species are evidence for natural selection, and they suggest that predators are a selective agent favouring the higher-spined morphs. We discuss these results with respect to the idea that geographic variation in Pun gidus reflects historical processes of isolation and differentiation during the Pleistocene era. 1. INTRODUCTION A powerful method for detecting the action of natural selection is to search for covariation among homologous polymorphic traits in closely related and ecologically similar species where they coexist (Clarke, 1975; Koehn and Mitton, 1972; Turner 1977). -
Contrasts Among Trait Categories in an Adaptive Radiation
Heredity (2015) 115, 335–348 & 2015 Macmillan Publishers Limited All rights reserved 0018-067X/15 www.nature.com/hdy REVIEW Iterative development and the scope for plasticity: contrasts among trait categories in an adaptive radiation SA Foster1, MA Wund2, MA Graham1, RL Earley3, R Gardiner2, T Kearns2 and JA Baker1 Phenotypic plasticity can influence evolutionary change in a lineage, ranging from facilitation of population persistence in a novel environment to directing the patterns of evolutionary change. As the specific nature of plasticity can impact evolutionary consequences, it is essential to consider how plasticity is manifested if we are to understand the contribution of plasticity to phenotypic evolution. Most morphological traits are developmentally plastic, irreversible, and generally considered to be costly, at least when the resultant phenotype is mis-matched to the environment. At the other extreme, behavioral phenotypes are typically activational (modifiable on very short time scales), and not immediately costly as they are produced by constitutive neural networks. Although patterns of morphological and behavioral plasticity are often compared, patterns of plasticity of life history phenotypes are rarely considered. Here we review patterns of plasticity in these trait categories within and among populations, comprising the adaptive radiation of the threespine stickleback fish Gasterosteus aculeatus. We immediately found it necessary to consider the possibility of iterated development, the concept that behavioral and life history trajectories can be repeatedly reset on activational (usually behavior) or developmental (usually life history) time frames, offering fine tuning of the response to environmental context. Morphology in stickleback is primarily reset only in that developmental trajectories can be altered as environments change over the course of development. -
A Field Guide to Fish Invaders of the Great Lakes Region
Non-Native Fish and Native Look-a-Likes A Component of the Aquatic Invasive Species-Hazard Analysis and Critical Control Point (AIS-HACCP) Program Fish Invaders This guide highlights harmful HACCP) training workshops, aquatic invasive fish that pose curriculum, video ( From Net to threats to the recreational, Sale ), and other program environmental, and economic materials. For details, visit value of the Great Lakes region. www.seagrant.umn.edu/ais/ Similar-looking native species haccp. are included for comparison. Specimens of non-native fish The non-native species identi - are needed to confirm sightings fied in this guide could spread and infestations, but many during harvest, stocking, or Great Lakes jurisdictions have fishery and law enforcement differing rules regarding operations. These fishes have possession and transport. Some the potential to displace native non-natives represented in species, harm habitats, and this field guide are regulated degrade lakes, rivers, streams, under state or provincial laws. and wetlands. Other non-native or native species can be harvested, trans - The purpose of this guide is to ported, or sold commercially. assist private and public fisheries personnel in identifying and Contact your local natural reporting potentially invasive resource management agency fish species. It is also designed for instructions. Never dump to accompany Aquatic Invasive live fish from one body of water Species-Hazard Analysis and into another without a permit. Critical Control Point (AIS- This Field Guide Contains: • Full-color illustrations for 38 invasive and common look-a-like fishes • Key characteristics to aid accurate identification* *Size estimates taken from Page, L. M. and B. -
ANNUAL REPORT Director’S Message
2017 ANNUAL REPORT Director’s Message Amanda in Howe Sound, British Columbia, Canada. Photo by Amanda Vincent/ Dear friends Project Seahorse I am so pleased to share some of the Project Seahorse findings and doings from 2017. It was a rich and full year, not least because I was on sabbatical from my UBC professorial post from September to December. That meant I could spend time on field visits and policy development, both of which I love. It also meant I had time and opportunity to refl ect on marine conservation in general and on our Project Seahorse work in particular. Allow me to share a few of those experiences and thoughts. Six weeks in India, the majority of it surveying bottom trawl landing sites with Tanvi Vaidyanathan, hugely supported Project Seahorse’s decision to throw a lot of time and eff ort at ending this absurdly wasteful method of extracting marine life. It’s time to target our take and stop trawling. Five weeks in southern Chile and Argentina allowed me to wallow in marine wildlife and help support the most southerly populations of seahorses in the new world. It was clear from working with Diego Luzzatto (IUCN SSC Specialist Group member) that the Project Seahorse combination of a research and management feedback loop would serve the Patagonian seahorses very well. Five weeks in China gave me hope that the country might be mobilizing for marine conservation. Xiong Zhang and I spent time encouraging better enforcement of new laws directed at phasing out bottom trawling, planning the establishment of MPAs and training young colleagues who will fight for the ocean. -
A Global Revision of the Seahorses Hippocampus Rafinesque 1810 (Actinopterygii: Syngnathiformes): Taxonomy and Biogeography with Recommendations for Further Research
Zootaxa 4146 (1): 001–066 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4146.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:35E0DECB-20CE-4295-AE8E-CB3CAB226C70 ZOOTAXA 4146 A global revision of the Seahorses Hippocampus Rafinesque 1810 (Actinopterygii: Syngnathiformes): Taxonomy and biogeography with recommendations for further research SARA A. LOURIE1,2, RILEY A. POLLOM1 & SARAH J. FOSTER1, 3 1Project Seahorse, Institute for the Oceans and Fisheries, The University of British Columbia, 2202 Main Mall, Vancouver, BC, V6T 1Z4, Canada 2Redpath Museum, 859 Sherbrooke Street West, Montreal, Quebec, H3A 2K6, Canada 3Corresponding author. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by E. Hilton: 2 Jun. 2016; published: 29 Jul. 2016 SARA A. LOURIE, RILEY A. POLLOM & SARAH J. FOSTER A global revision of the Seahorses Hippocampus Rafinesque 1810 (Actinopterygii: Syngnathiformes): Taxonomy and biogeography with recommendations for further research (Zootaxa 4146) 66 pp.; 30 cm. 1 Aug. 2016 ISBN 978-1-77557-509-2 (paperback) ISBN 978-1-77557-534-4 (Online edition) FIRST PUBLISHED IN 2016 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/j/zt © 2016 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing.