The Application of Genetics to Marine Management and Conservation: Examples from the Indo-Pacific
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Appendix 4: Background Materials Provided to Participants Prior to the Workshop
Appendix 4: Background materials provided to participants prior to the workshop. Coral reef fin fish spawning closures f. Camouflage grouper (Epinephelus polyphekadion) Risk assessment workshop g. Flowery cod (Epinephelus fuscoguttatus) h. Greasy rockcod (Epinephelus tauvina) 12 – 13 May 2009 i. Spanish flag (stripey;Lutjanus carponotatus) 9am – 5pm Russell 1 & 2 j. Tuskfish Choerodon( spp.) Berkley’s On Ann Closures targeting coral trout afford some protection Rendezvous Hotel Brisbane to other coral reef fin fish species, although the magnitude of this effect is speculative. The imperative 255 Ann Street, Brisbane to explicitly consider other species rests on judgments concerning • the importance of each species to each sector, • the importance of each sector, and • the capacity of existing controls other than spawning closures to provide adequate protection. These judgments are a central theme of the workshop. Background An initial task for the workshop is identification of candidate alternatives. Any closure regime This workshop will explore candidate alternatives for implemented beyond 2008 needs to provide adequate spawning closures to be applied 2009 – 2013. protection for spawning coral reef fin fish species, The Fisheries (Coral Reef Fin Fish) Management Plan within a constraint that the impost on commercial 2003 introduced three nine-day spawning closures and recreational (including charter) fishing is no for coral reef fin fish on the Great Barrier Reef (GBR). greater than for the period 2004 – 2008. ReefMAC The closures applied to the new moon periods in has recommended a five year package comprising two October, November and December for the years years (2009-2010) of no spawning closures followed 2004-2008. -
Target Fish Carnivores
TARGET FISH CARNIVORES WRASSES - LABRIDAE Thicklips Hemigymnus spp. Slingjaw Wrasse Epibulus insidiator Tripletail Wrasse Cheilinus trilobatus Redbreasted Wrasse Cheilinus fasciatus Barefoot Conservation | TARGET FISH CARNIVORES| July 2016 1 Hogfish Bodianus spp. Tuskfish Choerodon spp. Moon Wrasse Thalassoma lunare Humphead Wrasse Cheilinus undulatus Barefoot Conservation | TARGET FISH CARNIVORES| July 2016 2 GOATFISH - MULLIDAE Dash-dot Goatfish Parupeneus barberinus Doublebar Goatfish Parupeneus bifasciatus Manybar Goatfish Parupeneus multifasciatus SNAPPER - LUTJANIDAE Midnight Snapper Macolor macularis Barefoot Conservation | TARGET FISH CARNIVORES| July 2016 3 Spanish Flag Snapper Lutjanus carponotatus Black-banded Snapper Lutjanus semicinctus Checkered Snapper Lutjanus decussatus Two-spot Snapper Lutjanus biguttatus Red Snapper Lutjanus bohar Barefoot Conservation | TARGET FISH CARNIVORES| July 2016 4 GROUPER – SERRANIDAE Barramundi Cod Cromileptes altivelis Bluespotted Grouper Cephalopholis cyanostigma Peacock Grouper Cephalopholis argus Coral Grouper Cephalopholis miniata Barefoot Conservation | TARGET FISH CARNIVORES| July 2016 5 Lyretails Variola albimarginata & Variola louti Honeycomb Grouper Epinephelus merra Highfin Grouper Epinephelus maculatus Flagtail Grouper Cephalopholis urodeta Barefoot Conservation | TARGET FISH CARNIVORES| July 2016 6 Blacksaddle Coral Grouper Plectropomus laevis Large Groupers TRIGGERFISH - BALISTIDAE Titan Triggerfish Balistoides viridescens Barefoot Conservation | TARGET FISH CARNIVORES| July -
Reef Snappers (Lutjanidae)
#05 Reef snappers (Lutjanidae) Two-spot red snapper (Lutjanus bohar) Mangrove red snapper Blacktail snapper (Lutjanus argentimaculatus) (Lutjanus fulvus) Common bluestripe snapper (Lutjanus kasmira) Humpback red snapper Emperor red snapper (Lutjanus gibbus) (Lutjanus sebae) Species & Distribution Habitats & Feeding The family Lutjanidae contains more than 100 species of Although most snappers live near coral reefs, some species tropical and sub-tropical fi sh known as snappers. are found in areas of less salty water in the mouths of rivers. Most species of interest in the inshore fi sheries of Pacifi c Islands belong to the genus Lutjanus, which contains about The young of some species school on seagrass beds and 60 species. sandy areas, while larger fi sh may be more solitary and live on coral reefs. Many species gather in large feeding schools One of the most widely distributed of the snappers in the around coral formations during daylight hours. Pacifi c Ocean is the common bluestripe snapper, Lutjanus kasmira, which reaches lengths of about 30 cm. The species Snappers feed on smaller fi sh, crabs, shrimps, and sea snails. is found in many Pacifi c Islands and was introduced into They are eaten by a number of larger fi sh. In some locations, Hawaii in the 1950s. species such as the two-spot red snapper, Lutjanus bohar, are responsible for ciguatera fi sh poisoning (see the glossary in the Guide to Information Sheets). #05 Reef snappers (Lutjanidae) Reproduction & Life cycle Snappers have separate sexes. Smaller species have a maximum lifespan of about 4 years and larger species live for more than 15 years. -
The NATIONAL HORTICULTURAL MAGAZINE
NATIONAL GARDEN WEEK: APRIL 20th TO 26th VOLUME II-No. 4 Fall and Winter, 1923 The NATIONAL HORTICULTURAL MAGAZINE Dc','oted 10 the poplllari:::iJlg of all phases of horticlIlture: Ornamental Gardening, including La,nd sca/'f' GardeJl iJlg, ,·ll1latellr Flo'll'er GardeJling; Professioi/al Flower Gardi!'Jl iJl g or Floriculture; V egetable Garde Jl ing; Fruit Gro'willg, alld all acti'l'ilies allied with horticulture, Fall afld Winter Number CONTENTS Woods Flowers in Cultivation North Dakota State Horticultural Society Grand Forks Horticultural Society Galesburg Horticultural Society Wild lings of North America Garden Gossip Literature of the Trade Issued Quarterly and O'wned Exclusively by THE NATIONAL HORTICULTURAL SOCIETY OF AMERICA. , Permanent Headquarters to be Establishel at vVashington, D. C. Office of the Secretary, Henning, Minnesota 25 CENTS A COPY THE NATIONAL HORTICULTURAL SOCIETY OF AMERICA INCORPORATED .JULY 1, 1922 OFFICERS OF THE NATIONAL HORTICULTURAL SOCIETY PRESIDENT, Mr. C. Z. Nelson, VrCE PRESIDENT, Mrs. F a nnie Mahood Heath, Galesburg, Ill. Grand Forks, N . D. REGIONAL VICE PRESIDENTS NORTH PACIFIC' COAST: NORTHWEST MIDLAND: SOUTHEASTLAND: Mr. Joe Smith, Longbranch, Wash. Mrs. Mathilda C. Engstad, 703 So. Fifth Mrs. D . F . Sheppard, Daisy, Ga. St., Grand Forks, N. D. SOUTH PACIFIC COAST: N ORTHEAST MIDLAND: EASTERN CANADA: Mrs. E v a Kenworthy Gray, 32 and Wool Mr. O. H . Schroeder, Fariba ult, ¥inn. m a n Ave., San Diego, Cal. Dr. Frank E . Bennett, St. Thomas, Onto SOUTHWEST MIDLAND: NORTH ROCKY MOUNTAINS : Mrs. May Senn , Rota n , Tex. WESTERN CANADA: Mrs. Walter E . R evo, Glacier National SOUTHEAST M1DLAND: Mrs. -
Haliotis Asinina) in Coastal Waters of Thailand Determined Using Microsatellite Markers
Mar. Biotechnol. 6, 604–611, 2004 DOI: 10.1007/s10126-004-2300-5 Ó 2005 Springer Science+Business Media, Inc. Population Structure of Tropical Abalone (Haliotis asinina) in Coastal Waters of Thailand Determined Using Microsatellite Markers S. Tang,1 A. Tassanakajon,1 S. Klinbunga,2 P. Jarayabhand,3,4 and P. Menasveta2,4 1Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand 2Marine Biotechnology Research Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency, Pathumthani 12120, Thailand 3Aquatic Resources Research Institute, Chulalongkorn University, Bangkok 10330, Thailand 4Department of Marine Science, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand Abstract: Three partial genomic libraries were constructed from genomic DNA of the tropical abalone (Haliotis asinina) that was digested with AluI, vortexed/sonicated, and digested with mixed enzyme (AluI, HincII, and RsaI). The libraries yielded 0.02%, 0.42%, and 1.46% positive microsatellite-containing clones, respectively. Eleven clones each of perfect, imperfect, and compound microsatellites were isolated. Ten primer pairs (CU- Has1–CUHas10) were analyzed to evaluate their polymorphic level. The numbers of alleles per locus, observed heterozygosity (H0), and expected heterozygosity (He) ranged from 3 to 26 alleles, and varied between 0.27 and 0.85 and between 0.24 and 0.93, respectively. Three microsatellite loci (CUHas2, CUHas3, and CUHas8) were further used for examination of genetic diversity and differentiation of natural H. asinina in coastal waters of Thailand. Genetic variabilities in terms of the effective number of alleles (ne), H0, and He were higher in 2 samples from the Gulf of Thailand (ne = 9.37, 7.66; H0 = 0.62, 0.78; and He = 0.87, 0.86) than those of one sample (ne = 6.04; H0 = 0.58; and He = 0.62) derived from the Andaman Sea. -
Endangered Species Research 38:135
Vol. 38: 135–145, 2019 ENDANGERED SPECIES RESEARCH Published March 14 https://doi.org/10.3354/esr00942 Endang Species Res OPENPEN ACCESSCCESS Substantial impacts of subsistence fishing on the population status of an Endangered reef predator at a remote coral atoll Robert J. Lennox1,2,*, Alexander Filous2,3,4, Steven J. Cooke1, Andy J. Danylchuk2,3 1Fish Ecology and Conservation Physiology Laboratory, Department of Biology, Carleton University, Ottawa, Ontario K1S 5B6, Canada 2Indifly, PO Box 4460, St Paul, Minnesota 55104, USA 3Department of Environmental Conservation, University of Massachusetts Amherst, 160 Holdsworth Way, Amherst, Massachusetts 01003, USA 4The Island Initiative, Papeete, French Polynesia ABSTRACT: Napoleon wrasse Cheilinus undulatus has declined drastically throughout most of its range, owing, in large part, to overexploitation. In Anaa, French Polynesia, the species is har- vested as part of the subsistence catch by fishers using rockpile traps, spearguns, handmade har- poons, and baited handlines. We sampled 70 Napoleon wrasse captured by artisanal fishers of Anaa between 2015 and 2018 to assess the status of this population, and we applied data-poor fisheries models to assess the stock status of this iconic reef predator. The species was determined to be overexploited at a rate of 0.82 based on values of natural (0.14; Hoenig method) and fishing (0.58; difference of total and natural mortality) mortality as components of total mortality (0.72; Beverton-Holt estimation). The left-skewed length distribution (mean = 36 ± 13 cm SL) suggested an under-representation of large adults in the population, which would predominantly be terminal males in this sequentially hermaphroditic protogynous fish. -
Phylum MOLLUSCA
285 MOLLUSCA: SOLENOGASTRES-POLYPLACOPHORA Phylum MOLLUSCA Class SOLENOGASTRES Family Lepidomeniidae NEMATOMENIA BANYULENSIS (Pruvot, 1891, p. 715, as Dondersia) Occasionally on Lafoea dumosa (R.A.T., S.P., E.J.A.): at 4 positions S.W. of Eddystone, 42-49 fm., on Lafoea dumosa (Crawshay, 1912, p. 368): Eddystone, 29 fm., 1920 (R.W.): 7, 3, 1 and 1 in 4 hauls N.E. of Eddystone, 1948 (V.F.) Breeding: gonads ripe in Aug. (R.A.T.) Family Neomeniidae NEOMENIA CARINATA Tullberg, 1875, p. 1 One specimen Rame-Eddystone Grounds, 29.12.49 (V.F.) Family Proneomeniidae PRONEOMENIA AGLAOPHENIAE Kovalevsky and Marion [Pruvot, 1891, p. 720] Common on Thecocarpus myriophyllum, generally coiled around the base of the stem of the hydroid (S.P., E.J.A.): at 4 positions S.W. of Eddystone, 43-49 fm. (Crawshay, 1912, p. 367): S. of Rame Head, 27 fm., 1920 (R.W.): N. of Eddystone, 29.3.33 (A.J.S.) Class POLYPLACOPHORA (=LORICATA) Family Lepidopleuridae LEPIDOPLEURUS ASELLUS (Gmelin) [Forbes and Hanley, 1849, II, p. 407, as Chiton; Matthews, 1953, p. 246] Abundant, 15-30 fm., especially on muddy gravel (S.P.): at 9 positions S.W. of Eddystone, 40-43 fm. (Crawshay, 1912, p. 368, as Craspedochilus onyx) SALCOMBE. Common in dredge material (Allen and Todd, 1900, p. 210) LEPIDOPLEURUS, CANCELLATUS (Sowerby) [Forbes and Hanley, 1849, II, p. 410, as Chiton; Matthews. 1953, p. 246] Wembury West Reef, three specimens at E.L.W.S.T. by J. Brady, 28.3.56 (G.M.S.) Family Lepidochitonidae TONICELLA RUBRA (L.) [Forbes and Hanley, 1849, II, p. -
Christmas Island Biodiversity Monitoring Program: December 2003 to April 2007
Christmas Island Biodiversity Monitoring Program: December 2003 to April 2007 Report to the Department of Finance and Deregulation, from the Director of National Parks September 2008 2 Christmas Island Biodiversity Monitoring Program Project Contributions Project coordination: D.J. James; Field survey: D.J. James, K. Retallick; Data management, GIS: D.J. James, K. Retallick; Analyses and reporting: D.J. James Citation This document can be cited as: Christmas Island Biodiversity Monitoring Program: December 2003 to April 2007. Report to the Department of Finance and Deregulation from the Director of National Parks © Director of National Parks 2008 Christmas Island Biodiversity Monitoring Program 3 Contents EXECUTIVE SUMMARY ........................................................................................................................7 1. INTRODUCTION.................................................................................................................................9 1.1 Checklist of flora and fauna of Christmas Island.....................................................................9 1.2 Christmas Island biodiversity inventory database.................................................................10 2. CHRISTMAS ISLAND PIPISTRELLE ........................................................................................11 2.1 Summary of the results .........................................................................................................11 2.2 Research and monitoring methods .......................................................................................12 -
Evolution of Large Body Size in Abalones (Haliotis): Patterns and Implications
Paleobiology, 31(4), 2005, pp. 591±606 Evolution of large body size in abalones (Haliotis): patterns and implications James A. Estes, David R. Lindberg, and Charlie Wray Abstract.ÐKelps and other ¯eshy macroalgaeÐdominant reef-inhabiting organisms in cool seasÐ may have radiated extensively following late Cenozoic polar cooling, thus triggering a chain of evolutionary change in the trophic ecology of nearshore temperate ecosystems. We explore this hypothesis through an analysis of body size in the abalones (Gastropoda; Haliotidae), a widely distributed group in modern oceans that displays a broad range of body sizes and contains fossil representatives from the late Cretaceous (60±75 Ma). Geographic analysis of maximum shell length in living abalones showed that small-bodied species, while most common in the Tropics, have a cosmopolitan distribution, whereas large-bodied species occur exclusively in cold-water ecosys- tems dominated by kelps and other macroalgae. The phylogeography of body size evolution in extant abalones was assessed by constructing a molecular phylogeny in a mix of large and small species obtained from different regions of the world. This analysis demonstrates that small body size is the plesiomorphic state and largeness has likely arisen at least twice. Finally, we compiled data on shell length from the fossil record to determine how (slowly or suddenly) and when large body size arose in the abalones. These data indicate that large body size appears suddenly at the Miocene/Pliocene boundary. Our ®ndings support the view that ¯eshy-algal dominated ecosys- tems radiated rapidly in the coastal oceans with the onset of the most recent glacial age. -
Morphology and Early Life History Pattern of Some Lutjanus Species: a Review
INT. J. BIOL. BIOTECH., 8 (3): 455-461, 2011. MORPHOLOGY AND EARLY LIFE HISTORY PATTERN OF SOME LUTJANUS SPECIES: A REVIEW *Zubia Masood and Rehana Yasmeen Farooq Department of Zoology, University of Karachi, Karachi-75270, Pakistan. *email: [email protected] ABSTRACT The present study was based on the literature review of the fishes belonging to the snapper family Lutjanidae. Data parameters about the morphology and early life history pattern not measured during the survey were taken from the FishBase data base (see www.fishbase.org and Froese et al., 2000). These data parameters included, Lmax (maximum length), Linf (length infinity); K (growth rate); M (natural mortality); LS (life span); Lm (length at maturity); tm (age at first maturity); to (age at zero length); tmax (longevity) and also the morphological data. Morphological and life history data were taken only for five species of fishes belongs to genus Lutjanus i.e., L.johnii, L.malabaricus, L.lutjanus, L.fulvus, L.russellii. The main objective of this study was to review some aspects of distribution, morphology and feeding habits, spawning and also acquired and analyze information on selected life history variables to described patterns of variation among different species of snappers. Keywords: Lutjanidae, morphology, life history. INTRODUCTION This family is commonly known as “Snappers” are perch-like fishes, moderately elongated, fairly compressed (Allen and Talbot, 1985). Small to large fishes, ranging from 15cm-120cm or 1m in length and 40 kg in weight. Mouth is terminal, jaw bear large canine teeth (no canines in Apherius); Preopercle usually serrate. Dorsal fin continuous or slightly notched with 10-12 spines and 10-17 soft rays; anal fin with 3 spines and 7-11 soft rays; pelvic fins originating just behind pectoral base. -
Full Text (PDF)
Int. J. Dev. Biol. 53: 1081-1088 (2009) DEVELOPMENTALTHE INTERNATIONAL JOURNAL OF doi: 10.1387/ijdb.082791sc BIOLOGY www.intjdevbiol.com Expression of prohormone convertase 2 and the generation of neuropeptides in the developing nervous system of the gastropod Haliotis SCOTT F. CUMMINS1, PATRICK S. YORK1, PETER J. HANNA2, BERNARD M. DEGNAN1 and ROGER P. CROLL*,3 1School of Integrative Biology, The University of Queensland, Brisbane, Australia, 2School of Life and Environmental Sciences, Deakin University, Geelong, Australia and Department of Anatomy, Mahidol University, Bangkok, Thailand, 3Department of Physiology and Biophysics, Faculty of Medicine, Dalhousie University, Halifax, Canada ABSTRACT Prohormone convertase 2 (PC2) belongs to a family of enzymes involved in the proteolytic maturation of neuropeptide precursors into mature peptides that act as neurotrans- mitters, neuromodulators or neurohormones. Here we show that a gene encoding a PC2-like enzyme (HasPC2) is expressed during larval development and in the adult ganglia of the vetigastropod Haliotis asinina. HasPC2 exhibits high sequence identity to other gastropod PC2s and thus is likely to function in peptide processing. Analysis of HasPC2 expression indicates that it is activated early in nervous system development. During trochophore and early veliger larval stages, HasPC2 is expressed in the vicinity of the forming ganglia of the central nervous system and parts of the putative peripheral nervous system. Later in larval development, at the time the veliger becomes competent to interact with the external environment and initiate metamorpho- sis, HasPC2 expression largely restricts to cells of the major ganglia and their commissures. Profiling of veliger larvae by bioinformatic approaches suggests the expression of a variety of peptides. -
Final Corals Supplemental Information Report
Supplemental Information Report on Status Review Report And Draft Management Report For 82 Coral Candidate Species November 2012 Southeast and Pacific Islands Regional Offices National Marine Fisheries Service National Oceanic and Atmospheric Administration Department of Commerce Table of Contents INTRODUCTION ............................................................................................................................................. 1 Background ............................................................................................................................................... 1 Methods .................................................................................................................................................... 1 Purpose ..................................................................................................................................................... 2 MISCELLANEOUS COMMENTS RECEIVED ...................................................................................................... 3 SRR EXECUTIVE SUMMARY ........................................................................................................................... 4 1. Introduction ........................................................................................................................................... 4 2. General Background on Corals and Coral Reefs .................................................................................... 4 2.1 Taxonomy & Distribution .............................................................................................................