Lobster Fishery in NSW
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Proceedings of the American Samoa Coral Reef Fishery Workshop
Proceedings of the American Samoa Coral Reef Fishery Workshop Stacey Kilarski and Alan R. Everson (Editors) U.S. Department of Commerce National Oceanic and Atmospheric Administration National Marine Fisheries Service NOAA Technical Memorandum NMFS-F/SPO-114 Proceedings of the American Samoa Coral Reef Fishery Workshop Convention Center, Utulei, American Samoa October 21-23, 2008 Edited by: Stacey Kilarksi AECOS, Inc. 45-939 Kamehameha Highway Suite 104 Kane‘ohe, HI 96744 Alan R. Everson Pacific Islands Regional Office, NMFS Habitat Conservation Division 1601 Kapiolani Blvd Suite 1110 Honolulu, HI 96814 [email protected] NOAA Technical Memorandum NMFS-F/SPO-114 U.S. Department of Commerce Gary Locke, Secretary of Commerce National Oceanic and Atmospheric Administration Jane Lubchenco, Ph.D., Administrator of NOAA National Marine Fisheries Service Eric C. Schwaab, Assistant Administrator for Fisheries Suggested citation: Kilarski, Stacey, and Alan Everson (eds.). Proceedings of the American Samoa Coral Reef Fishery Workshop (October 2008). U.S. Dep. Commerce, NOAA Tech. Memo. NMFS- F/SPO114, 143 p. A copy of this report may be obtained from: Alan R. Everson Pacific Islands Regional Office, NMFS Habitat Conservation Division 1601 Kapiolani Blvd Suite 1110 Honolulu, HI 96814 [email protected] Or online at: http://spo.nmfs.noaa.gov/tm/ American Samoa Coral Reef Fishery Workshop Convention Center, Utulei, American Samoa October 21-23, 2008 Organizers: NOAA-Pacific Island Regional Office NOAA-Pacific Island Fishery Science Center Department -
Assessing the Effectiveness of Surrogates for Conserving Biodiversity in the Port Stephens-Great Lakes Marine Park
Assessing the effectiveness of surrogates for conserving biodiversity in the Port Stephens-Great Lakes Marine Park Vanessa Owen B Env Sc, B Sc (Hons) School of the Environment University of Technology Sydney Submitted in fulfilment for the requirements of the degree of Doctor of Philosophy September 2015 Certificate of Original Authorship I certify that the work in this thesis has not been previously submitted for a degree nor has it been submitted as part of requirements for a degree except as fully acknowledged within the text. I also certify that the thesis has been written by me. Any help that I have received in my research work and preparation of the thesis itself has been acknowledged. In addition, I certify that all information sources and literature used as indicated in the thesis. Signature of Student: Date: Page ii Acknowledgements I thank my supervisor William Gladstone for invaluable support, advice, technical reviews, patience and understanding. I thank my family for their encouragement and support, particularly my mum who is a wonderful role model. I hope that my children too are inspired to dream big and work hard. This study was conducted with the support of the University of Newcastle, the University of Technology Sydney, University of Sydney, NSW Office of the Environment and Heritage (formerly Department of Environment Climate Change and Water), Marine Park Authority NSW, NSW Department of Primary Industries (Fisheries) and the Integrated Marine Observing System (IMOS) program funded through the Department of Industry, Climate Change, Science, Education, Research and Tertiary Education. The sessile benthic assemblage fieldwork was led by Dr Oscar Pizarro and undertaken by the University of Sydney’s Australian Centre for Field Robotics. -
Table of Fishes of Sydney Harbour 2019
Table of Fishes of Sydney Harbour 2019 Family Family/Com Species Species Common Notes mon Name Name Acanthuridae Surgeonfishe Acanthurus Eyestripe close s dussumieri Surgeonfish to southern li mit Acanthuridae Acanthurus Orangebloch close to olivaceus Surgeonfish southern limit Acanthuridae Acanthurus Convict close to triostegus Surgeonfish southern limit Acanthuridae Acanthurus Yellowmask xanthopterus Surgeonfish Acanthuridae Paracanthurus Blue Tang not included hepatus in species count Acanthuridae Prionurus Spotted Sawtail maculatus Acanthuridae Prionurus Australian Sawtail microlepidotus Ambassidae Glassfishes Ambassis Port Jackson jacksoniensis glassfish Ambassidae Ambassis marianus Estuary Glassfish Anguillidae Freshwater Anguilla australis Shortfin Eel Eels Anguillidae Anguilla reinhardtii Longfinned Eel Antennariidae Anglerfishes Antennarius Freckled Anglerfish southern limit coccineus Antennariidae Antennarius Giant Anglerfish close to commerson southen limit Antennariidae Antennarius Shaggy Anglerfish southern limit hispidus Antennariidae Antennarius pictus Painted Anglerfish Antennariidae Antennarius striatus Striate Anglerfish Table of Fishes of Sydney Harbour 2019 Antennariidae Histrio histrio Sargassum close to Anglerfish southen limit Antennariidae Porophryne Red-fingered erythrodactylus Anglerfish Aploactinidae Velvetfishes Aploactisoma Southern Velvetfish milesii Aploactinidae Cocotropus Patchwork microps Velvetfish Aploactinidae Paraploactis Bearded Velvetfish trachyderma Aplodactylidae Seacarps Aplodactylus Rock Cale -
Catalogue of Protozoan Parasites Recorded in Australia Peter J. O
1 CATALOGUE OF PROTOZOAN PARASITES RECORDED IN AUSTRALIA PETER J. O’DONOGHUE & ROBERT D. ADLARD O’Donoghue, P.J. & Adlard, R.D. 2000 02 29: Catalogue of protozoan parasites recorded in Australia. Memoirs of the Queensland Museum 45(1):1-164. Brisbane. ISSN 0079-8835. Published reports of protozoan species from Australian animals have been compiled into a host- parasite checklist, a parasite-host checklist and a cross-referenced bibliography. Protozoa listed include parasites, commensals and symbionts but free-living species have been excluded. Over 590 protozoan species are listed including amoebae, flagellates, ciliates and ‘sporozoa’ (the latter comprising apicomplexans, microsporans, myxozoans, haplosporidians and paramyxeans). Organisms are recorded in association with some 520 hosts including mammals, marsupials, birds, reptiles, amphibians, fish and invertebrates. Information has been abstracted from over 1,270 scientific publications predating 1999 and all records include taxonomic authorities, synonyms, common names, sites of infection within hosts and geographic locations. Protozoa, parasite checklist, host checklist, bibliography, Australia. Peter J. O’Donoghue, Department of Microbiology and Parasitology, The University of Queensland, St Lucia 4072, Australia; Robert D. Adlard, Protozoa Section, Queensland Museum, PO Box 3300, South Brisbane 4101, Australia; 31 January 2000. CONTENTS the literature for reports relevant to contemporary studies. Such problems could be avoided if all previous HOST-PARASITE CHECKLIST 5 records were consolidated into a single database. Most Mammals 5 researchers currently avail themselves of various Reptiles 21 electronic database and abstracting services but none Amphibians 26 include literature published earlier than 1985 and not all Birds 34 journal titles are covered in their databases. Fish 44 Invertebrates 54 Several catalogues of parasites in Australian PARASITE-HOST CHECKLIST 63 hosts have previously been published. -
AUSTRALIAN NATIONAL SPEARFISHING RECORDS JULY 2018 COMPILED by AUF RECORDS OFFICER VIN RUSHWORTH Common Names
AUSTRALIAN NATIONAL SPEARFISHING RECORDS JULY 2018 COMPILED BY AUF RECORDS OFFICER VIN RUSHWORTH Common Names Common Name Pg. Common Name Pg. Albacore 37 Cod, Barramundi 39 Amberjack 8 Cod, Bearded 27 Amberjack, High-fin 9 Cod, Black 40 Angelfish Yellow-Mask 32 Cod, Blacksaddle Rock 40 Angelfish, Blue 32 Cod, Blackspotted 40 Angelfish, Imperial 32 Cod, Black-Tipped Rock 40 Angelfish, Six Banded 32 Cod, Break-Sea 39 Anglerfish, Spinycoat 3 Cod, Camouflage 40 Barracouta 13 Cod, Chinaman 41 Barracuda, Blackfin 44 Cod, Coral 39 Barracuda, Blue and Gold 44 Cod, Coral Rock 39 Barracuda, Chevron 44 Cod, Dusky 42 Barracuda, Great 44 Cod, Flowery 40 Barracuda, Pickhandle 44 Cod, Freckled Coral 39 Barramundi 20 Cod, Gold Spotted 39 Bass, Red 23 Cod, Highfin 40 Batfish, Black-tip 13 Cod, Long-finned Rock 41 Batfish, Hump-headed 13 Cod, Long-headed 41 Batfish, Long-finned 13 Cod, Maori 41 Batfish, Long-snout 13 Cod, Masked 41 Batfish, Short-finned 13 Cod, Ocellated 39 Bigeye, Lunar-tailed 33 Cod, Peacock Coral 39 Blackfish, Banded Rock 14 Cod, Potato 41 Blackfish, Rock 14 Cod, Pug-Nosed Wire-netting 40 Blackfish, Western Rock 14 Cod, Purple 40 Blanquillo, Blue 25 Cod, Rankin 40 Blue Devil, Eastern 31 Cod, Red 27 Blue Devil, Southern 31 Cod, Red Rock 37 Bluefish 13 Cod, Red Rock Western 38 Blue-lined Seabream 24 Cod, Red-flushed Rock 38 Boarfish, Giant 30 Cod, Speckledfin 40 Boarfish, Longsnout 30 Cod, Tomato Coral 39 Boarfish, Short 30 Cod, Twin-Spot 39 Boarfish, Yellow-spotted 30 Cod, White-lined Rock 38 Bonefish, Eastern 3 Coral Fish, New-moon -
Giant Boarfish
148 analis (Waite) and P.compressa (White). Family Kyphosidae - sea chubs and rudderfishes This family contains about a dozen widespread species. They are thickly built, oval shaped fish which frequent coral reefs and rocky shores in most tropical and subtropical seas. In general, kyphosids are herbivorous, feeding on algae and other marine growth, although some species are planktivorous. The jaws possess incisor-like teeth at the front. These may be serrated, loosely attached and movable, or may be fixed. There are no molars. Other characteristics of this family are the complete, slightly arched lateral line and the single dorsal fin. Many of these fish will often follow ships, hence the common name !rudderfish1. Six species occur in New Zealand. Those found in the Reserve, parore, Girella tricuspidata, silver drummer, typhosus Sydney onus, sweep, Scorpis aequipinnis and blue maomao, S.violaceus, are common northern New Zealand species. The other two, the mado, Atypichthys striagatus, and the bluefish, Girella oyanea, are commonly found around the north-east offshore islands, but are rare on the coast. There is some argument surrounding the classification of the sweep, S.aequipinnis, and blue maomao, 5.violaceus. Many consider them to be different morphs of the same species. Others distinguish them as two different species. The two are similar in appearance and in meristic characteristics such as the numbers of fin rays and lateral line scales. Recently, Smith et al (1979) suggested that they should be treated as two separate species on the basis of electrophoretio analysis, body colour, head shape and the characteristic number of gill rakers. -
Biology, Stock Status and Management Summaries for Selected Fish Species in South-Western Australia
Fisheries Research Report No. 242, 2013 Biology, stock status and management summaries for selected fish species in south-western Australia Claire B. Smallwood, S. Alex Hesp and Lynnath E. Beckley Fisheries Research Division Western Australian Fisheries and Marine Research Laboratories PO Box 20 NORTH BEACH, Western Australia 6920 Correct citation: Smallwood, C. B.; Hesp, S. A.; and Beckley, L. E. 2013. Biology, stock status and management summaries for selected fish species in south-western Australia. Fisheries Research Report No. 242. Department of Fisheries, Western Australia. 180pp. Disclaimer The views and opinions expressed in this publication are those of the authors and do not necessarily reflect those of the Department of Fisheries Western Australia. While reasonable efforts have been made to ensure that the contents of this publication are factually correct, the Department of Fisheries Western Australia does not accept responsibility for the accuracy or completeness of the contents, and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of, or reliance on, the contents of this publication. Fish illustrations Illustrations © R. Swainston / www.anima.net.au We dedicate this guide to the memory of our friend and colleague, Ben Chuwen Department of Fisheries 3rd floor SGIO Atrium 168 – 170 St Georges Terrace PERTH WA 6000 Telephone: (08) 9482 7333 Facsimile: (08) 9482 7389 Website: www.fish.wa.gov.au ABN: 55 689 794 771 Published by Department of Fisheries, Perth, Western Australia. Fisheries Research Report No. 242, March 2013. ISSN: 1035 - 4549 ISBN: 978-1-921845-56-7 ii Fisheries Research Report No.242, 2013 Contents ACKNOWLEDGEMENTS ............................................................................................... -
Evidence of Connectivity Between Juvenile and Adult Habitats for Mobile Marine Fauna: an Important Component of Nurseries
MARINE ECOLOGY PROGRESS SERIES Vol. 247: 281–295, 2003 Published February 4 Mar Ecol Prog Ser REVIEW Evidence of connectivity between juvenile and adult habitats for mobile marine fauna: an important component of nurseries Bronwyn M. Gillanders1,*, Kenneth W. Able2, Jennifer A. Brown3, David B. Eggleston4, Peter F. Sheridan5 1Department of Environmental Biology, University of Adelaide, Adelaide, South Australia 5005, Australia 2Marine Field Station, Institute of Marine and Coastal Sciences, Rutgers University, 800 c/o 132 Great Bay Boulevard, Tuckerton, New Jersey 08087, USA 3A316 Earth and Marine Sciences Building, EE Biology, University of California, Santa Cruz, California 95064, USA 4North Carolina State University, Department of Marine, Earth and Atmospheric Sciences, Raleigh, North Carolina 27695-8208, USA 5NOAA Fisheries, Southeast Fisheries Science Center, 3500 Delwood Beach Road, Panama City, Florida 32408, USA ABSTRACT: A critical link missing from our understanding of the nursery role of specific marine habitats is the evidence of connectivity between juvenile and adult habitats. This paper reviews and evaluates evidence of, and spatial scales for, movements from juvenile to adult habitats and it sum- marises the methods used to study movements. Examples include many fish families but few inverte- brate taxa, and most are species of economic importance for USA and Australia. The types of juvenile habitat range from the entire estuary or shallow open coastal waters to specific habitats within estu- aries or coastal waters; in some cases juvenile habitats include habitats not traditionally regarded as nursery areas (e.g. the surf zone). The duration of time spent in juvenile habitats averages 13 mo (range 8 d to 5 yr). -
Longterm Shifts in Abundance and Distribution of a Temperate Fish Fauna
Global Ecology and Biogeography, (Global Ecol. Biogeogr.) (2011) 20, 58–72 RESEARCH Long-term shifts in abundance and PAPER distribution of a temperate fish fauna: a response to climate change and fishing practicesgeb_575 58..72 Peter R. Last1,2*, William T. White1,2, Daniel C. Gledhill1,2, Alistair J. Hobday1,2, Rebecca Brown3, Graham J. Edgar3 and Gretta Pecl3 1Climate Adaptation Flagship, CSIRO Marine ABSTRACT and Atmospheric Research, GPO Box 1538, Aim South-eastern Australia is a climate change hotspot with well-documented Hobart TAS 7001, Australia, 2Wealth from Oceans Flagship, CSIRO Marine and recent changes in its physical marine environment. The impact on and temporal Atmospheric Research, GPO Box 1538, Hobart responses of the biota to change are less well understood, but appear to be due to TAS 7001, Australia, 3Tasmanian Aquaculture influences of climate, as well as the non-climate related past and continuing human and Fisheries Institute, Private Bag 49, Hobart impacts. We attempt to resolve the agents of change by examining major temporal TAS 7001, Australia and distributional shifts in the fish fauna and making a tentative attribution of causal factors. Location Temperate seas of south-eastern Australia. Methods Mixed data sources synthesized from published accounts, scientific surveys, spearfishing and angling competitions, commercial catches and underwa- ter photographic records, from the ‘late 1800s’ to the ‘present’, were examined to determine shifts in coastal fish distributions. Results Forty-five species, representing 27 families (about 30% of the inshore fish families occurring in the region), exhibited major distributional shifts thought to be climate related. These are distributed across the following categories: species previously rare or unlisted (12), with expanded ranges (23) and/or abundance increases (30), expanded populations in south-eastern Tasmania (16) and extra- limital vagrants (4). -
Les Genres Et Sous-Genres De Chaetodontidés Étudiés Par Une Méthode D'analyse Numérique
Bull. Mus. natn. Hist, nat., Paris, 4e sér., 6, 1984, section A, n° 2 : 453-485. Les genres et sous-genres de Chaetodontidés étudiés par une méthode d'analyse numérique par André MAUGÉ et Roland BAUCHOT Résumé. — L'analyse en composantes principales des cent quinze espèces de Chaetodontidae à l'aide de trente variables (neuf valeurs méristiques, treize proportions de diverses parties du corps et huit caractères morphologiques) a permis de préciser, à partir de divers dendrogrammes, les affinités de ces espèces entre elles et de proposer une nouvelle répartition des Chaetodontidae en vingt genres, dont quatre nouveaux, et vingt et un sous-genres, dont six nouveaux. Abstract. — Principal component analysis of the 115 species of Chaetodontids using 30 varia- bles (9 meristic data, 13 proportions of different body parts and 8 morphological characters) allowed us to define, from the study of different dendrograms, the affinities of the species and to propose a new classification of the Chaetodontids in 20 genera (4 of which are new) and 21 sub-genera (6 of which are new). A. MAUGÉ, Laboratoire d'Ichtyologie générale et appliquée, Muséum national d'Histoire naturelle, 43, rue Cuvier, 75231 Paris cedex 05. R. BAUCHOT, Laboratoire d'Anatomie comparée, Université Paris VII, 2, place Jussieu, 75221 Paris cedex 05. La famille des chétodons (Chaetodontidae) a toujours formé un puzzle, dont tous les auteurs qui ont eu à en connaître depuis BLEEKER se sont efforcés de classer les éléments et d'harmoniser les sous-classements. Certains ont tenté cet effort pour une aire géogra- phique restreinte, fonction des limites des faunes envisagées. -
CHECKLIST of PROTOZOA RECORDED in AUSTRALASIA O'donoghue P.J. 1986
1 PROTOZOAN PARASITES IN ANIMALS Abbreviations KINGDOM PHYLUM CLASS ORDER CODE Protista Sarcomastigophora Phytomastigophorea Dinoflagellida PHY:din Euglenida PHY:eug Zoomastigophorea Kinetoplastida ZOO:kin Proteromonadida ZOO:pro Retortamonadida ZOO:ret Diplomonadida ZOO:dip Pyrsonymphida ZOO:pyr Trichomonadida ZOO:tri Hypermastigida ZOO:hyp Opalinatea Opalinida OPA:opa Lobosea Amoebida LOB:amo Acanthopodida LOB:aca Leptomyxida LOB:lep Heterolobosea Schizopyrenida HET:sch Apicomplexa Gregarinia Neogregarinida GRE:neo Eugregarinida GRE:eug Coccidia Adeleida COC:ade Eimeriida COC:eim Haematozoa Haemosporida HEM:hae Piroplasmida HEM:pir Microspora Microsporea Microsporida MIC:mic Myxozoa Myxosporea Bivalvulida MYX:biv Multivalvulida MYX:mul Actinosporea Actinomyxida ACT:act Haplosporidia Haplosporea Haplosporida HAP:hap Paramyxea Marteilidea Marteilida MAR:mar Ciliophora Spirotrichea Clevelandellida SPI:cle Litostomatea Pleurostomatida LIT:ple Vestibulifera LIT:ves Entodiniomorphida LIT:ent Phyllopharyngea Cyrtophorida PHY:cyr Endogenida PHY:end Exogenida PHY:exo Oligohymenophorea Hymenostomatida OLI:hym Scuticociliatida OLI:scu Sessilida OLI:ses Mobilida OLI:mob Apostomatia OLI:apo Uncertain status UNC:sta References O’Donoghue P.J. & Adlard R.D. 2000. Catalogue of protozoan parasites recorded in Australia. Mem. Qld. Mus. 45:1-163. 2 HOST-PARASITE CHECKLIST Class: MAMMALIA [mammals] Subclass: EUTHERIA [placental mammals] Order: PRIMATES [prosimians and simians] Suborder: SIMIAE [monkeys, apes, man] Family: HOMINIDAE [man] Homo sapiens Linnaeus, -
Myall Lakes Ramsar Site
Myall Lakes Ramsar site Ecological character description Myall Lakes Ramsar site Ecological character description Disclaimer The Office of Environment and Heritage NSW (OEH) has compiled this document in good faith, exercising all due care and attention. OEH does not accept responsibility for any inaccurate or incomplete information supplied by third parties. No representation is made about the accuracy, completeness or suitability of the information in this publication for any particular purpose. Readers should seek appropriate advice about the suitability of the information to their needs. The views and opinions expressed in this publication are those of the authors and do not necessarily reflect those of the Australian Government or the Minister for Sustainability, Environment, Water, Population and Communities. Acknowledgements This document has been compiled with the help of many people in NSW Government agencies, and other people with expertise in ecology, hydrology, geomorphology and limnology. Those people include Steve Smith, Fiona Miller and Susanne Callaghan, NSW National Parks and Wildlife Service; Peter Myerscough, Honorary Research Associate, University of Sydney; Matt Dasey, OEH; Peter Scanes, Kirsty Brennan, John Porter and Nick Carlile, Scientific Services, OEH; Matt Bell, Great Lakes Council; Meagan Callaghan, Manly Hydraulics Laboratory; Trudy Walford, NSW Department of Primary Industries; and David Turner. This publication has been prepared with funding provided by the Australian Government. Symbols for conceptual models are courtesy of the Integration and Application Network (ian.umces.edu/symbols), University of Maryland Center for Environmental Science. © State of NSW, Office of Environment and Heritage NSW. OEH is pleased to allow the reproduction of material from this publication on the condition that the source, publisher and authorship are appropriately acknowledged.