Aquaculture and Related Biological Attributes of Abalone Species in Australia – a Review
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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. -
Tracking Larval, Newly Settled, and Juvenile Red Abalone (Haliotis Rufescens ) Recruitment in Northern California
Journal of Shellfish Research, Vol. 35, No. 3, 601–609, 2016. TRACKING LARVAL, NEWLY SETTLED, AND JUVENILE RED ABALONE (HALIOTIS RUFESCENS ) RECRUITMENT IN NORTHERN CALIFORNIA LAURA ROGERS-BENNETT,1,2* RICHARD F. DONDANVILLE,1 CYNTHIA A. CATTON,2 CHRISTINA I. JUHASZ,2 TOYOMITSU HORII3 AND MASAMI HAMAGUCHI4 1Bodega Marine Laboratory, University of California Davis, PO Box 247, Bodega Bay, CA 94923; 2California Department of Fish and Wildlife, Bodega Bay, CA 94923; 3Stock Enhancement and Aquaculture Division, Tohoku National Fisheries Research Institute, FRA 3-27-5 Shinhamacho, Shiogama, Miyagi, 985-000, Japan; 4National Research Institute of Fisheries and Environment of Inland Sea, Fisheries Agency of Japan 2-17-5 Maruishi, Hatsukaichi, Hiroshima 739-0452, Japan ABSTRACT Recruitment is a central question in both ecology and fisheries biology. Little is known however about early life history stages, such as the larval and newly settled stages of marine invertebrates. No one has captured wild larval or newly settled red abalone (Haliotis rufescens) in California even though this species supports a recreational fishery. A sampling program has been developed to capture larval (290 mm), newly settled (290–2,000 mm), and juvenile (2–20 mm) red abalone in northern California from 2007 to 2015. Plankton nets were used to capture larval abalone using depth integrated tows in nearshore rocky habitats. Newly settled abalone were collected on cobbles covered in crustose coralline algae. Larval and newly settled abalone were identified to species using shell morphology confirmed with genetic techniques using polymerase chain reaction restriction fragment length polymorphism with two restriction enzymes. Artificial reefs were constructed of cinder blocks and sampled each year for the presence of juvenile red abalone. -
Quarantine Requirements for the Importation of Live Crustaceans and Molluscs
Quarantine Requirements for the Importation of Live Crustaceans and Molluscs (In case of any discrepancy between the English version and the Chinese text of these Requirements, the Chinese text shall govern.) Promulgated by Council of Agriculture on April 12, 2004 Amendment by Council of Agriculture on February 16, 2011 Amendment by Council of Agriculture on March 25, 2014 Amendment by Council of Agriculture on August 25, 2014 1. The scope of the species and listed diseases of live crustaceans and molluscs of this Requirements apply to are listed in the Attached tables of the Requirements. The applicant shall apply for an import permit from a central competent authority if the species of live crustaceans and molluscs are referred to Article 24 of Wildlife Conservation Act as protected wildlife or Article 27 as wildlife which are not domestic species. The importation of live crustaceans and molluscs for human consumption shall comply with Article 11 of Act Governing Food Sanitation. 2. The importation of live crustaceans and molluscs for aquaculture or rearing purpose shall comply with the following conditions: (1) Live crustaceans and molluscs shall be kept in the water area or aquaculture facility of origin approved by the exporting country for at least fourteen days prior to the shipment, where high mortality of unknown etiology has not occurred among live crustaceans and molluscs during the previous three months. (2) The water area or aquaculture facility of origin shall meet one of the following conditions: I. The following basic -
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. -
Sea Ranching Trials for Commercial Production of Greenlip (Haliotis Laevigata) Abalone in Western Australia
1 Sea ranching trials for commercial production of greenlip (Haliotis laevigata) abalone in Western Australia An outline of results from trials conducted by Ocean Grown Abalone Pty Ltd April 2013 Roy Melville-Smith1, Brad Adams2, Nicola J. Wilson3 & Louis Caccetta3 1Curtin University Department of Environment and Agriculture GPO Box U1987, Perth WA6845 2Ocean Grown Abalone Pty Ltd PO Box 231, Augusta WA6290 3Curtin University Department of Mathematics and Statistics GPO Box U1987, Perth WA6845 2 Table of Contents Abstract ............................................................................................................................................... 4 Acknowledgements ............................................................................................................................. 5 1 Introduction .................................................................................................................................... 6 2 Methods .......................................................................................................................................... 7 2.1 Seed stock production ................................................................................................................. 7 2.2 Transport of seed stock ................................................................................................................ 7 2.3 The study site ............................................................................................................................... 8 2.4 Habitat -
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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. -
W+W Special Paper B-18-2
W+W Special Paper B-18-2 DIE GENETISCHE FAMILIE DER HALIOTIDAE – HYBRIDISIERUNG, FORTPFLANZUNGSISOLATION UND SYMPATRISCHE ARTBILDUNG Nigel Crompton September 2018 http://www.wort-und-wissen.de/artikel/sp/b-18-2_haliotidae.pdf Bild: Doka54, Public Domain Inhalt Einleitung ................................................................................................ 3 Taxonomie der Seeohren ...................................................................... 6 Die taxonomische Stellung der Seeohren .........................................................7 Glossar ..............................................................................................................7 Seeohren-Arten und Hybriden ......................................................... 9 Genetische Familien und Befruchtung ..........................................14 Genetische Familien und sympatrische Artbildung ......................15 Die Rolle der Wechselwirkung zwischen Ei und Spermium bei der Befruchtung..............................................................................................16 Wechselwirkung zwischen Ei und Spermium und sympatrische Artbildung ....17 Besonderheiten der VERL-Lysin-Bindungsdomänen ......................................18 Wie kann es trotz Hybridisierung zur Artbildung kommen? ..........................19 Weitere Beispiele und vergleichbare Mechanismen bei Pflanzen ......................20 Schlussfolgerung .............................................................................21 Quellen ............................................................................................21 -
Blacklip Abalone (Haliotis Rubra) Exploitation Status Overfished to Recruitment Overfished
I & I NSW WILD FISHERIES RESEARCH PROGRAM Blacklip Abalone (Haliotis rubra) EXPLOITATION STATUS OVERFISHED TO RECRUITMENT OVERFISHED Stock is currently recovering from historically low levels that occurred due to a combination of overfishing and mortality due to the parasite Perkinsus sp. There are concerns about possible recruitment overfishing in the northern regions. SCIENTIFIC NAME STANDARD NAME COMMENT Haliotis rubra Blacklip abalone Haliotis rubra Image © Bernard Yau Background Blacklip abalone (Haliotis rubra) is a large, juveniles and adults all occur in the same flattened marine gastropod mollusc which habitat. This suggests that local recruitment occurs in rocky reef habitats on the south- is dependent on the proximity of adults. This, eastern Australian coastline from northern combined with the restricted movement NSW to Rottnest Island in Western Australia, of adult abalone, gives rise to stocks which including Tasmania. Blacklip abalone form are spatially highly structured. Increasingly the basis of the abalone fishery in NSW. The sophisticated management regimes are species is also harvested in the other southern being developed to properly account for this Australian states along with the greenlip structuring. abalone H. laevigata. The bulk of the Australian Commercially, blacklip abalone are harvested production of abalone is exported to lucrative by endorsed divers, usually using compressed markets in south-east Asia. air supplied from a hookah unit, although Blacklip abalone can live for over in some cases SCUBA or free diving may be 20 years and can reach a maximum size of used. A chisel shaped abalone iron is used to 22 cm shell length (SL) and a weight of over pry the abalone away from the rock surface. -
Status Review of the Pinto Abalone - Decision
Status Review of the Pinto Abalone - Decision TABLE OF CONTENTS Page Summary Sheet ............................................................................................................. 1 of 42 CR-102 ......................................................................................................................... 3 of 42 WAC 220-330-090 Crawfish, ((abalone,)) sea urchins, sea cucumbers, goose barnacles—Areas and seasons, personal-use fishery ........................................ 6 of 42 WAC 220-320-010 Shellfish—Classification .................................................................. 7 of 42 WAC 220-610-010 Wildlife classified as endangered species ....................................... 9 of 42 Status Report for the Pinto Abalone in Washington .................................................... 10 of 42 Summary Sheet Meeting dates: May 31, 2019 Agenda item: Status Review of the Pinto Abalone (Decision) Presenter(s): Chris Eardley, Puget Sound Shellfish Policy Coordinator Henry Carson, Fish & Wildlife Research Scientist Background summary: Pinto abalone are iconic marine snails prized as food and for their beautiful shells. Initially a state recreational fishery started in 1959; the pinto abalone fishery closed in 1994 due to signs of overharvest. Populations have continued to decline since the closure, most likely due to illegal harvest and densities too low for reproduction to occur. Populations at monitoring sites declined 97% from 1992 – 2017. These ten sites originally held 359 individuals and now hold 12. The average size of the remnant individuals continues to increase and wild juveniles have not been sighted in ten years, indicating an aging population with little reproduction in the wild. The species is under active restoration by the department and its partners to prevent local extinction. Since 2009 we have placed over 15,000 hatchery-raised juvenile abalone on sites in the San Juan Islands. Federal listing under the Endangered Species Act (ESA) was evaluated in 2014 but retained the “species of concern” designation only. -
Quarantine Requirements for the Importation of Live Crustaceans
Quarantine Requirements for the Importation of Live Crustaceans and Molluscs (In case of any discrepancy between the English version and the Chinese text of these Requirements, the Chinese text shall govern.) Promulgated by Council of Agriculture on April 12, 2004 Amendment by Council of Agriculture on February 16, 2011 Amendment by Council of Agriculture on March 25, 2014 Amendment by Council of Agriculture on August 25, 2014 Amendment by Council of Agriculture on August 25, 2014 Amendment by Council of Agriculture on June 30, 2018 and become effective on September 1, 2018 1. The scope of species and pertinent diseases of concern of crustaceans and molluscs to which these Requirements apply is shown in the attached Tables 1 and 2. 2. Sample collection, testing and surveillance as referred to in these Requirements must be conducted in accordance with relevant provisions in the Manual of Diagnostic Tests for Aquatic Animals of the World Organisation for Animal Health (hereinafter referred to as the OIE Aquatic Manual). For diseases with no sampling, testing or surveillance methods prescribed in the OIE Aquatic Manual, methods that have been published in international scientific journals are to be used. Disease incubation periods referred to in these Requirements are those specified in the OIE Aquatic Manual or the Aquatic Animal Health Code of the OIE (hereinafter referred to as the OIE Aquatic Code). For diseases with incubation periods not specified in the OIE Aquatic Manual or OIE Aquatic Code, incubation periods stated in articles published in international scientific journals shall apply. If no such information can be found either in the OIE Aquatic Manual, OIE Aquatic Code or international scientific journals, the incubation period will be 30 days. -
BMC Biology Biomed Central
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by GEO-LEOe-docs BMC Biology BioMed Central Research article Open Access A rapidly evolving secretome builds and patterns a sea shell Daniel J Jackson1,2, Carmel McDougall1,4, Kathryn Green1, Fiona Simpson3, Gert Wörheide2 and Bernard M Degnan*1 Address: 1School of Integrative Biology, University of Queensland, Brisbane Qld 4072, Australia, 2Department of Geobiology, Geoscience Centre, University of Göttingen, Goldschmidtstr.3, 37077 Göttingen, Germany, 3Institute of Molecular Biosciences, University of Queensland, Brisbane Qld 4072, Australia and 4Department of Zoology, University of Oxford, Tinbergen Bldg., South Parks Road, Oxford OX1 3PS, UK Email: Daniel J Jackson - [email protected]; Carmel McDougall - [email protected]; Kathryn Green - [email protected]; Fiona Simpson - [email protected]; Gert Wörheide - [email protected] goettingen.de; Bernard M Degnan* - [email protected] * Corresponding author Published: 22 November 2006 Received: 27 July 2006 Accepted: 22 November 2006 BMC Biology 2006, 4:40 doi:10.1186/1741-7007-4-40 This article is available from: http://www.biomedcentral.com/1741-7007/4/40 © 2006 Jackson et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Instructions to fabricate mineralized structures with distinct nanoscale architectures, such as seashells and coral and vertebrate skeletons, are encoded in the genomes of a wide variety of animals. -
Growth-Related Gene Expression in Haliotis Midae
GROWTH‐RELATED GENE EXPRESSION IN HALIOTIS MIDAE Mathilde van der Merwe Dissertation presented for the degree of Doctor of Philosophy (Genetics) at Stellenbosch University Promoter: Dr Rouvay Roodt‐Wilding Co‐promoters: Dr Stéphanie Auzoux‐Bordenave and Dr Carola Niesler December 2010 Declaration By submitting this dissertation, I declare that the entirety of the work contained therein is my own, original work, that I am the authorship owner thereof (unless to the extent explicitly otherwise stated) and that I have not previously in its entirety or in part submitted it for obtaining any qualification. Date: 09/11/2010 Copyright © 2010 Stellenbosch University All rights reserved I Acknowledgements I would like to express my sincere gratitude and appreciation to the following persons for their contribution towards the successful completion of this study: Dr Rouvay Roodt‐Wilding for her continued encouragement, careful attention to detail and excellent facilitation throughout the past years; Dr Stéphanie Auzoux‐Bordenave for valuable lessons in abalone cell culture and suggestions during completion of the manuscript; Dr Carola Niesler for setting an example and providing guidance that already started preparing me for a PhD several years ago; Dr Paolo Franchini for his patience and greatly valued assistance with bioinformatics; Dr Aletta van der Merwe and my fellow lab‐colleagues for their technical and moral support; My dear husband Willem for his love, support and enthusiasm, for sitting with me during late nights in the lab and for making me hundreds of cups of tea; My parents for their love and encouragement and for instilling the determination in me to complete my studies; All my family and friends for their sincere interest.