Oren SONIN 1, Pierre SALAMEH 1, and Daniel GOLANI 2*
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Skeletal Development and Mineralization Pattern of The
e Rese tur arc ul h c & a u D q e A v e f l o o Mesa-Rodríguez et al., J Aquac Res Development 2014, 5:6 l p a m n Journal of Aquaculture r e u n o t DOI: 10.4172/2155-9546.1000266 J ISSN: 2155-9546 Research & Development Research Article OpenOpen Access Access Skeletal Development and Mineralization Pattern of the Vertebral Column, Dorsal, Anal and Caudal Fin Complex in Seriola Rivoliana (Valenciennes, 1833) Larvae Mesa-Rodríguez A*, Hernández-Cruz CM, Socorro JA, Fernández-Palacios H, Izquierdo MS and Roo J Aquaculture Research Group, Science and Technology Park, University of Las Palmas de Gran Canaria, P. O. Box 56, 35200 Telde, Canary Islands, Spain Abstract Bone and fins development in Seriola rivoliana were studied from cleared and stained specimens from 3 to 33 days after hatching. The vertebral column began to mineralize in the neural arches at 4.40 ± 0.14 mm Standard Length (SL), continued with the haemal arches and centrums following a cranial-caudal direction. Mineralization of the caudal fin structures started with the caudal rays by 5.12 ± 0.11 mm SL, at the same time that the notochord flexion occurs. The first dorsal and anal fin structures were the hard spines (S), and lepidotrichium (R) by 8.01 ± 0.26 mm SL. The metamorphosis was completed by 11.82 ± 0.4 mm SL. Finally, the fin supports (pterygiophores) and the caudal fins were completely mineralized by 16.1 ± 0.89 mm SL. In addition, the meristic data of 23 structures were provided. -
Seriola Dumerili (Greater Amberjack)
UWI The Online Guide to the Animals of Trinidad and Tobago Diversity Seriola dumerili (Greater Amberjack) Family: Carangidae (Jacks and Pompanos) Order: Perciformes (Perch and Allied Fish) Class: Actinopterygii (Ray-finned Fish) Fig. 1. Greater amberjack, Seriola dumerili. [http://portal.ncdenr.org/web/mf/amberjack_greater downloaded 20 October 2016] TRAITS. The species Seriola dumerili displays rapid growth during development as a juvenile progressing to an adult. It is the largest species of the family of jacks. At adulthood, S. dumerili would typically weigh about 80kg and reach a length of 1.8-1.9m. Sexual maturity is achieved between the age of 3-5 years, and females may live longer and grow larger than males (FAO, 2016). S. dumurili are rapid-moving predators as shown by their body form (Fig. 1) (FLMNH, 2016). The adult is silvery-bluish in colour, whereas the juvenile is yellow-green. It has a characteristic goldish side line, as well as a dark band near the eye, as seen in Figs 1 and 2 (FAO, 2016; MarineBio, 2016; NCDEQ, 2016). DISTRIBUTION. S. dumerili is native to the waters of Trinidad and Tobago. Typically pelagic, found between depths of 10-360m, the species can be described as circumglobal. In other words, it is found worldwide, as seen in Fig. 3, though much more rarely in some areas, for example the eastern Pacific Ocean (IUCN, 2016). Due to this distribution, there is no threat to the population of the species, despite overfishing in certain locations. Migrations do occur, which are thought to be linked to reproductive cycles. -
Morphological Development of Embryo, Larvae and Juvenile in Yellowtail Kingfish, Seriola Lalandi
Dev. Reprod. Vol. 20, No. 2, 131~140, June, 2016 http://dx.doi.org/10.12717/DR.2016.20.2.131 ISSN 2465-9525 (Print) ISSN 2465-9541 (Online) Morphological Development of Embryo, Larvae and Juvenile in Yellowtail Kingfish, Seriola lalandi Sang Geun Yang1, Sang Woo Hur2, Seung Cheol Ji1, Sang Gu Lim1, Bong Seok Kim1, Minhwan Jeong1, Chi Hoon Lee2 and †Young-Don Lee2 1Jeju Fisheries Research Institute, National Institute of Fisheries Science, Jeju 63610, Korea 2Marine Science Institute, Jeju National University, Jeju 63333, Korea ABSTRACT : This study monitored the morphological development of embryo, larvae and juvenile yellowtail kingfish, Seriola lalandi, for their aquaculture. The fertilized eggs obtained by natural spawning were spherical shape and buoyant. Fertilized eggs were transparent and had one oil globule in the yolk, with an egg diameter of 1.35 ± 0.04 mm and an oil globule diameter of 0.32 ± 0.02 mm. The fertilized eggs hatched 67–75 h after fertilization in water at 20 ± 0.5°C. The total length (TL) of the hatched larvae was 3.62 ± 0.16 mm. During hatching, the larvae, with their mouth and anus not yet opened. The yolk was completely absorbed 3 days after hatching (DAH), while the TL of post-larvae was 4.72 ± 0.07 mm. At 40 DAH, the juveniles had grown to 30.44 ± 4.07 mm in TL, body depth increased, the body color changed to a black, yellow, and light gray-blue color, and 3–4 vertical stripes appeared. At 45 DAH, the juveniles were 38.67 ± 5.65 mm in TL and 10.10 ± 0.94 mm in body depth. -
Morphological Development of Embryo, Larvae and Juvenile in Yellowtail Kingfish, Seriola Lalandi
Dev. Reprod. Vol. 20, No. 2, 109~118, June, 2016 http://dx.doi.org/10.12717/DR.2016.20.2.109 ISSN 2465-9525 (Print) ISSN 2465-9541 (Online) Morphological Development of Embryo, Larvae and Juvenile in Yellowtail kingfish, Seriola lalandi Sang Geun Yang1, Sang Woo Hur2, Seung Cheol Ji1, Sang Gu Lim1, Bong Seok Kim1, Minhwan Jeong1, Chi Hoon Lee2 and †Young-Don Lee2 1Jeju Fisheries Research Institute, National Institute of Fisheries Science, Jeju 63610, Korea 2Marine Science Institute, Jeju National University, Jeju 63333, Korea ABSTRACT : This study monitored the morphological development of embryo, larvae and juvenile yellowtail kingfish, Seriola lalandi, for their aquaculture. The fertilized eggs obtained by natural spawning were spherical shape and buoyant. Fertilized eggs were transparent and had one oil globule in the yolk, with an egg diameter of 1.35 ± 0.04 mm and an oil globule diameter of 0.32 ± 0.02 mm. The fertilized eggs hatched 67–75 h after fertilization in water at 20 ± 0.5°C. The total length (TL) of the hatched larvae was 3.62 ± 0.16 mm. During hatching, the larvae, with their mouth and anus not yet opened. The yolk was completely absorbed 3 days after hatching (DAH), while the TL of post-larvae was 4.72 ± 0.07 mm. At 40 DAH, the juveniles had grown to 30.44 ± 4.07 mm in TL, body depth increased, the body color changed to a black, yellow, and light gray-blue color, and 3–4 vertical stripes appeared. At 45 DAH, the juveniles were 38.67 ± 5.65 mm in TL and 10.10 ± 0.94 mm in body depth. -
© Iccat, 2007
A5 By-catch Species APPENDIX 5: BY-CATCH SPECIES A.5 By-catch species By-catch is the unintentional/incidental capture of non-target species during fishing operations. Different types of fisheries have different types and levels of by-catch, depending on the gear used, the time, area and depth fished, etc. Article IV of the Convention states: "the Commission shall be responsible for the study of the population of tuna and tuna-like fishes (the Scombriformes with the exception of Trichiuridae and Gempylidae and the genus Scomber) and such other species of fishes exploited in tuna fishing in the Convention area as are not under investigation by another international fishery organization". The following is a list of by-catch species recorded as being ever caught by any major tuna fishery in the Atlantic/Mediterranean. Note that the lists are qualitative and are not indicative of quantity or mortality. Thus, the presence of a species in the lists does not imply that it is caught in significant quantities, or that individuals that are caught necessarily die. Skates and rays Scientific names Common name Code LL GILL PS BB HARP TRAP OTHER Dasyatis centroura Roughtail stingray RDC X Dasyatis violacea Pelagic stingray PLS X X X X Manta birostris Manta ray RMB X X X Mobula hypostoma RMH X Mobula lucasana X Mobula mobular Devil ray RMM X X X X X Myliobatis aquila Common eagle ray MYL X X Pteuromylaeus bovinus Bull ray MPO X X Raja fullonica Shagreen ray RJF X Raja straeleni Spotted skate RFL X Rhinoptera spp Cownose ray X Torpedo nobiliana Torpedo -
The Biology and Ecology of Samson Fish Seriola Hippos
The biology of Samson Fish Seriola hippos with emphasis on the sportfishery in Western Australia. By Andrew Jay Rowland This thesis is presented for the degree of Doctor of Philosophy at Murdoch University 2009 DECLARATION I declare that the information contained in this thesis is the result of my own research unless otherwise cited. ……………………………………………………. Andrew Jay Rowland 2 Abstract This thesis had two overriding aims. The first was to describe the biology of Samson Fish Seriola hippos and therefore extend the knowledge and understanding of the genus Seriola. The second was to uses these data to develop strategies to better manage the fishery and, if appropriate, develop catch-and-release protocols for the S. hippos sportfishery. Trends exhibited by marginal increment analysis in the opaque zones of sectioned S. hippos otoliths, together with an otolith of a recaptured calcein injected fish, demonstrated that these opaque zones represent annual features. Thus, as with some other members of the genus, the number of opaque zones in sectioned otoliths of S. hippos are appropriate for determining age and growth parameters of this species. Seriola hippos displayed similar growth trajectories to other members of the genus. Early growth in S. hippos is rapid with this species reaching minimum legal length for retention (MML) of 600mm TL within the second year of life. After the first 5 years of life growth rates of each sex differ, with females growing faster and reaching a larger size at age than males. Thus, by 10, 15 and 20 years of age, the predicted fork lengths (and weights) for females were 1088 (17 kg), 1221 (24 kg) and 1311 mm (30 kg), respectively, compared with 1035 (15 kg), 1124 (19 kg) and 1167 mm (21 kg), respectively for males. -
Capture-Based Aquaculture of Yellowtail
199 Capture-based aquaculture of yellowtail Makoto Nakada Tokyo University of Marine Science and Technology Tokyo, Japan E-mail: [email protected] Nakada, M. 2008. Capture-based aquaculture of yellowtail. In A. Lovatelli; P.F. Holthus (eds). Capture-based aquaculture. Global overview. FAO Fisheries Technical Paper. No. 508. Rome, FAO. pp. 199–215. SUMMARY The 2004 production of cultured yellowtail (Seriola spp.) in Japan from 1 288 enterprises was 150 028 tonnes valued at ¥111.2 billion (US$1.334 billion). Yellowtail mariculture has developed remarkably due to the abundant supply and low price of wild-caught juveniles (Mojako) and sardines used as the main fish feed of fishmeal component. Hatchery produced yellowtail seed are far more expensive. Other critical elements that supported the growth of yellowtail farming include the existence of abundant suitable culture sites along the Japanese coast and innovative technical developments. The history of yellowtail culture in Japan began over 70 years ago. Before that, fishers cultured undersized fish in ponds and sold them when they reached marketable size. This utilization of bycatch (undersized fish) was accepted by the public, particularly as unmarketable fish were often used as fertilizer or livestock feed. Currently aquaculture production for many species exceeds that landed from capture fisheries. Some commercial culture trials on amberjack have been undertaken in Taiwan Province of China, Mexico and Vietnam, but no successes have been achieved with raising yellowtail. The main constraints include diseases and low production costs in tropical areas. In contrast, the culture of Seriola spp. is promising due to their strong vitality and rapid growth, and may well expand at the global level through hatchery-produced juveniles. -
The Evolutionary History of the Genus Seriola and the Phylogeography and Genetic Diversity of S. Lalandi (Yellowtail) Across
The evolutionary history of the genus Seriola and the phylogeography and genetic diversity of S. lalandi (yellowtail) across its distribution range By Belinda Louisa Swart Dissertation presented for the degree of Doctor of Philosophy in the Faculty of Genetics at Stellenbosch University Supervisor: Prof. Rouvay Roodt-Wilding Co-supervisor: Dr. Aletta E. Bester-van der Merwe Dr. Sophie von der Heyden April 2014 1 Stellenbosch University http://scholar.sun.ac.za Declaration By submitting this thesis electronically, I declare that the entirety of the work contained therein is my own, original work, that I am the sole author thereof (save to the extent explicitly otherwise stated), that reproduction and publication thereof by Stellenbosch University will not infringe any third party rights and that I have not previously in its entirety or in part submitted it for obtaining any qualification. April 2014 Copyright © 2014 Stellenbosch University All rights reserved 1 Stellenbosch University http://scholar.sun.ac.za Abstract The genus Seriola includes several important commercial fish species, yet the phylogenetic relationships between species have not been fully investigated to date. This study reports the first molecular phylogeny for this genus based on two mitochondrial (Cytb and COI) and two nuclear gene (RAG1 and Rhod) fragments for all extant Seriola species (nine species, n = 27). The phylogenetic patterns resolved three main lineages: a ((S. fasciata and S. peruana), S. carpenteri) clade, a (S. dumerili and S. rivoliana) clade and a (S. lalandi and S. quinqueradiata) clade. The closure of the Tethys Sea (12 - 20 MYA) coincides with divergence of the ((S. fasciata and S. -
Dimorphisme Sexuel Et Caractérisation Biométrique De La Sériole
Available online at http://www.ifgdg.org Int. J. Biol. Chem. Sci. 15(2): 728-736, April 2021 ISSN 1997-342X (Online), ISSN 1991-8631 (Print) Original Paper http://ajol.info/index.php/ijbcs http://indexmedicus.afro.who.int Dimorphisme sexuel et caractérisation biométrique de la Sériole guinéenne, Seriola carpenteri, (Mather 1971) échantillonné dans la Zone Economique Exclusive (ZEE) de la Côte d’Ivoire Laizih Yves-Armand ATTEMENE 1*, Yao Laurent ALLA2, Jean Noel YAPI1, Melecony Célestin BLE2 et Kouakou YAO1 1 Laboratoire de Biologie et Cytologie Animales, UFR-SN, Université Nangui Abrogoua (Ex-Université d’Abobo- Adjamé), 02 BP 801 Abidjan 02, Côte d’Ivoire. 2 Centre de Recherches Océanologiques, Département Aquaculture, BP V 18 Abidjan, Côte d’Ivoire. * Auteur correspondant ; E-mail : [email protected] Received: 24-01-2021 Accepted: 25-04-2021 Published: 30-04-2021 RESUME La reproduction artificielle des poissons en captivité nécessite la connaissance de leur dimorphisme sexuel. La détermination du dimorphisme sexuel de la Sériole Guinéenne, Seriola carpenteri est difficile à travers l'examen de l'orifice urogénital. Cette étude a pour but de déterminer le dimorphisme sexuel et les caractéristiques biométriques chez Seriola carpenteri (Mather, 1971) échantillonnée dans la Zone Économique Exclusive (ZEE) ivoirienne, dans le Golfe de guinée. Ainsi, un échantillonnage de 360 spécimens de Seriola carpenteri (Mather, 1971) encore appelé Sériole guinéenne a été effectué en raison de 30 individus par mois pendant la période allant d’août 2017 à juillet 2018. Le poids et la longueur standard des spécimens variaient respectivement de 300,2 g à 935 g et de 22,8 cm à 36,2 cm. -
Shallow Seamounts Represent Speciation Islands for Circumglobal
www.nature.com/scientificreports OPEN Shallow seamounts represent speciation islands for circumglobal yellowtail Seriola lalandi Sven Kerwath1,2,8*, Rouvay Roodt‑Wilding3, Toufek Samaai2,4, Henning Winker1, Wendy West1, Sheroma Surajnarayan5, Belinda Swart3, Aletta Bester‑van der Merwe3, Albrecht Götz6, Stephen Lamberth1,7 & Christopher Wilke1 Phenotypic plasticity in life‑history traits in response to heterogeneous environments has been observed in a number of fshes. Conversely, genetic structure has recently been detected in even the most wide ranging pelagic teleost fsh and shark species with massive dispersal potential, putting into question previous expectations of panmixia. Shallow oceanic seamounts are known aggregation sites for pelagic species, but their role in genetic structuring of widely distributed species remains poorly understood. The yellowtail kingfsh (Seriola lalandi), a commercially valuable, circumglobal, epipelagic fsh species occurs in two genetically distinct Southern Hemisphere populations (South Pacifc and southern Africa) with low levels of gene‑fow between the regions. Two shallow oceanic seamounts exist in the ocean basins around southern Africa; Vema and Walters Shoal in the Atlantic and Indian oceans, respectively. We analysed rare samples from these remote locations and from the South African continental shelf to assess genetic structure and population connectivity in S. lalandi and investigated life‑history traits by comparing diet, age, growth and maturation among the three sites. The results suggest that yellowtail from South Africa and the two seamounts are genetically and phenotypically distinct. Rather than mere feeding oases, we postulate that these seamounts represent islands of breeding populations with site‑specifc adaptations. Seamounts have long been known as aggregation sites for large pelagic fshes such as tuna, billfshes and sharks1. -
Alien Species in the Mediterranean Sea by 2010
Mediterranean Marine Science Review Article Indexed in WoS (Web of Science, ISI Thomson) The journal is available on line at http://www.medit-mar-sc.net Alien species in the Mediterranean Sea by 2010. A contribution to the application of European Union’s Marine Strategy Framework Directive (MSFD). Part I. Spatial distribution A. ZENETOS 1, S. GOFAS 2, M. VERLAQUE 3, M.E. INAR 4, J.E. GARCI’A RASO 5, C.N. BIANCHI 6, C. MORRI 6, E. AZZURRO 7, M. BILECENOGLU 8, C. FROGLIA 9, I. SIOKOU 10 , D. VIOLANTI 11 , A. SFRISO 12 , G. SAN MART N 13 , A. GIANGRANDE 14 , T. KATA AN 4, E. BALLESTEROS 15 , A. RAMOS-ESPLA ’16 , F. MASTROTOTARO 17 , O. OCA A 18 , A. ZINGONE 19 , M.C. GAMBI 19 and N. STREFTARIS 10 1 Institute of Marine Biological Resources, Hellenic Centre for Marine Research, P.O. Box 712, 19013 Anavissos, Hellas 2 Departamento de Biologia Animal, Facultad de Ciencias, Universidad de Ma ’laga, E-29071 Ma ’laga, Spain 3 UMR 6540, DIMAR, COM, CNRS, Université de la Méditerranée, France 4 Ege University, Faculty of Fisheries, Department of Hydrobiology, 35100 Bornova, Izmir, Turkey 5 Departamento de Biologia Animal, Facultad de Ciencias, Universidad de Ma ’laga, E-29071 Ma ’laga, Spain 6 DipTeRis (Dipartimento per lo studio del Territorio e della sue Risorse), University of Genoa, Corso Europa 26, 16132 Genova, Italy 7 Institut de Ciències del Mar (CSIC) Passeig Mar tim de la Barceloneta, 37-49, E-08003 Barcelona, Spain 8 Adnan Menderes University, Faculty of Arts & Sciences, Department of Biology, 09010 Aydin, Turkey 9 c\o CNR-ISMAR, Sede Ancona, Largo Fiera della Pesca, 60125 Ancona, Italy 10 Institute of Oceanography, Hellenic Centre for Marine Research, P.O. -
Seriola Lalandi Dorsalis), Technological Advances Towards the Development of the Aquaculture Sector
Quantifying Digestion in California Yellowtail (Seriola lalandi dorsalis), Technological Advances Towards the Development of the Aquaculture Sector The Graduate Division The University of Hawai‘i at Hilo In Partial Fulfillment of the Requirements for the Degree of Master of Science: Tropical Conservation Biology and Environmental Science Hilo, Hawai’i December 2016 By: George Rod Parish IV Thesis Committee: Armando Garciaa Charles Farwellbc Luke Gardnerbd Kevin Hopkinsa Barbara Blockbd a Pacific Aquaculture & Coastal Resources Center, College of Agriculture, Forestry and Natural Resource Management, University of Hawaii at Hilo, 1079 Kalanianaole Ave., Hilo, HI 96720, United States b Tuna Research and Conservation Center, 886 Cannery Row, Monterey, CA 93940, USA c Monterey Bay Aquarium, 886 Cannery Row, Monterey, CA 93940, USA d Biology Department, Hopkins Marine Station, Stanford University, 120 Ocean View Blvd, Pacific Grove, CA 93950, USA Table of Contents Acknowledgements ......................................................................................................................... iv List Of Figures .................................................................................................................................. vi List Of Tables .................................................................................................................................. vii Chapter 1: Introduction ................................................................................................................. 1 I. Yellowtail