Assessment of Coastal Fish in the Baltic Sea

Total Page:16

File Type:pdf, Size:1020Kb

Assessment of Coastal Fish in the Baltic Sea Baltic Sea Environment Proceedings No. 103 A Assessment of Coastal Fish in the Baltic Sea Helsinki Commission Baltic Marine Environment Protection Commission Baltic Sea Environment Proceedings No. 103 A Assessment of Coastal Fish in the Baltic Sea Helsinki Commission Baltic Marine Environment Protection Commission Authors: Kaj Ådjers1), Jan Andersson2), Magnus Appelberg3), Redik Eschbaum4), Ronald Fricke5), Antti Lappalainen6), Atis Minde7), Henn Ojaveer4), Wojciech Pelczarski8) and Rimantas Repečka9). 1)Co-ordination Organ for Baltic Reference Areas, Provincial Government of Åland Islands, Fisheries Division, P.O. Box 1060, AX-22111 Mariehamn, Åland Islands 2)Swedish Board of Fisheries, Institute of Coastal Research, Ävrö 16, S-572 95 Figeholm, Sweden 3)Swedish Board of Fisheries, Institute of Coastal Research, Box 109, S-74071 Öregrund, Sweden 4)Estonian Marine Institute, University of Tartu, Mäealuse 10 A, EE-12618 Tallinn, Estonia 5)State Museum of Natural History, Rosenstein 1, D-70191 Stuttgart, Germany 6)Finnish Game and Fisheries Research Institute, P.O. Box 6, FIN-00721 Helsinki, Finland 7)Latvian Fish Resources Agency, Daugavgrivas street 8, LV-1048 Riga, Latvia 8)Sea Fisheries Institute (MIR), Kollataja 1 Str, PL- 81332, Poland 9)Institute of Ecology, Vilnius University, Akademijos Street 2, LT-08412 Vilnius 21, Lithuania Language check: Janet Pawlak For bibliographic purposes this document should be cited as: HELCOM, 2006 Assessment of Coastal Fish in the Baltic Sea Balt. Sea Environ. Proc. No. 103 A Information included in this publication or extracts thereof is free for citing on the condition that the complete reference of the publication is given as stated above Copyright 2006 by the Baltic Marine Environment Protection Commission - Helsinki Commission - Cover photo: Johnny Jensen Design and layout: Bitdesign, Vantaa, Finland Printed by: DMP – Digital Media Partners Oy, Finland ISSN 0357-2994 Table of Contents Summary . 4 Introduction . 5 Sampling programme used in coastal fi sh monitoring . .6 Factors infl uencing the structure of the fi sh populations and communities in the Baltic Sea . 10 Temperature . 10 Salinity . 10 Eutrophication . .10 Fisheries . .11 Other important factors . 11 Ecological indicators . 13 Species richness . .13 Index of abundance . 13 Index of biomass . .14 Ratio between European perch/roach based on weight . 15 Trophic level of fi sh communities . 16 Piscivorous fi sh . 17 Threatened and declining species . 18 Non-indigenous fi sh . .19 Discussion and recommendations . 20 References . .22 Assessment of Coastal Fish in the Baltic Sea 3 Summary Coastal fi sh communities are important com- ence the structure of the local fi sh community. ponents of Baltic Sea ecosystems. These com- High fi shing pressure during the 1990s in the munities consist of fi sh of various origins: marine West-Estonian archipelago, which caused a col- species, freshwater species, migratory species, lapse in the coastal fi sh stocks, was apparent in and glacial relicts. Representatives of all these the monitoring catches. categories have different preferences for environ- mental conditions. For example, marine fi sh prefer The report recommends the inclusion of 34 spe- more saline areas, freshwater fi sh prefer less cies considered to be of high priority for conserva- saline areas, and glacial relicts are more abundant tion, 70 species of medium priority, and 80 species in cold-water layers in deeper areas. The compo- of low priority into the HELCOM Red List of threat- sition of coastal fi sh communities varies in the ened and declining Baltic fi sh species. Although different regions of the Baltic Sea in relation to the the spread of non-indigenous species has been different habitat characteristics of these regions, suggested to be among the most severe threats with salinity, water temperature, and nutrient to global biodiversity, the signifi cance of most availability among the important factors. Other non-indigenous fi sh species introduced into the important factors include seabed type for bottom- Baltic Sea remains of less importance since they dwelling fi sh, and algal and seagrass conditions in have failed to form self-sustaining populations. shallow waters for near-coastal species. However, two species, the accidentally introduced round goby (Neogobius melanostomus) and the Monitoring of coastal fi sh using multi-mesh gill- intentionally introduced Prussian carp (Carassius nets and gillnet series has been carried out in gibelio), are exceptions in this respect. In particu- fi fteen areas in the Baltic Sea. The objectives of lar, the round goby is spreading, and new records this monitoring are to describe and elucidate long- of its occurrence are reported every year. term trends in fi sh populations and fi sh community development, and to try to explain the results in relation to natural factors and anthropogenic pres- sures. This report covers current time series of varying length up to 22 years of annual monitoring. The development of coastal fi sh stocks has been evaluated using indicators such as species rich- ness, species abundance in terms of numbers and weight, a weight-based ratio between European perch and roach, trophic levels, the abundance of piscivorous fi sh, and the occurrence of non- indigenous species. A brief summary of the threat status of Baltic fi sh species is also presented. Signifi cant increasing trends in European perch and roach catches per unit effort have been observed in the Archipelago region between the southern Gulf of Bothnia and the northern Baltic Proper. A possible reason for these trends is ongoing coastal eutrophication as well as increased temperatures during the past decade. On the other hand, some roach populations in the Baltic Proper have shown decreasing trends in relative abundance. The Curonian lagoon and the river mouth of the Daugava are areas severely affected by anthropogenic impacts, which infl u- 4 Introduction The Baltic Sea ecosystems have undergone dra- the fi sh community, HELCOM is in the process of matic changes during the late 20th century, as a developing ecological quality objectives. Some result of both human activities and natural factors. suggested objectives have been presented in This is also true for the fi sh communities in coastal the “Discussions and recommendations” section areas. Coastal fi sh are subjected to a number of of this report. A number of potential indicators anthropogenic impacts such as enhanced nutri- that can be used for assessing ecological quality ent loads, contamination by heavy metals, organic objectives based on the coastal fi sh monitoring toxicants and hormone-like substances, as well as programme have been discussed in HELCOM the destruction of recruitment habitats. Changes workshops (BSRP/HELCOM, 2005). In this in mortality rates caused by increased fi shing assessment, a selected set of indicators has been pressure and increased predation by seals and proposed to describe the status of and temporal cormorants also infl uence fi sh community devel- trends in the coastal fi sh fauna in the Baltic Sea. opment. Changes related to the introduction of These indicators are: species richness, relative non-native species may also ultimately represent abundance (catch per unit effort) of species, the a substantial threat to the coastal fi sh fauna. ratio between functional groups, and the trophic level of fi sh communities. In an effort to improve the state of the Baltic marine environment, and thus also reduce pressures on Assessment of Coastal Fish in the Baltic Sea 5 Sampling programme used in coastal fi sh monitoring At present, a network of coastal fi sh monitoring areas covering large areas of the Baltic Sea is sampled annually. The network comprises moni- toring areas in Estonia, Finland, Latvia, Lithuania, Poland, and Sweden. Coastal areas in Denmark, Germany, and Russia are monitored as well, but have not been included in this assessment. This monitoring is coordinated by the “Co-ordination Organ for Baltic Reference Areas” (COBRA), which maintains a database containing coastal fi sh monitoring results collected from participating monitoring areas. The monitoring programme in 2005 covered fi fteen monitoring areas (Figure 1). Four of these include two sub-areas (Curonian lagoon, Hiiumaa, Kvädöfjärden, and Holmöarna) that represent different environmental conditions and, consequently, the fi sh communities may Figure 1. differ between these sub-areas. The time series Sampling cover variable periods, depending on area, up to locations for 22 years of annual monitoring, with the year 2004 coastal fi sh monitoring being the last year included in the present assess- under the ment. Four areas were added to the network in COBRA 2004: Torhamn in southern Sweden, Lagnö in the programme, northern archipelago of Stockholm, Haapasaaret including the gear in the Gulf of Finland, and Kumlinge in the eastern used and the archipelago of the Åland Islands. As the monitor- fi rst year of ing method in Poland differs markedly from the sampling. others, Polish results have not been included in Coastal fi sh monitoring in the Baltic Sea 2004 this report. Area Gear Start year Råneå Coastal survey nets 1994 The coastal fi sh monitoring programme is mainly Råneå Nordic coastal nets 2002 directed towards species of demersal fi sh (fi sh Holmöarna Coastal survey nets 1989 living close to the bottom) and benthopelagic fi sh Holmöarna Nordic coastal nets 2002 (fi sh living both close to the bottom and in the Forsmark Coastal survey nets 1983 open water) that live in coastal areas
Recommended publications
  • Parasite Communities and Feeding Ecology of the European Sprat (Sprattus Sprattus L.) Over Its Range of Distribution
    Parasitol Res (2012) 110:1147–1157 DOI 10.1007/s00436-011-2605-z ORIGINAL PAPER Parasite communities and feeding ecology of the European sprat (Sprattus sprattus L.) over its range of distribution Sonja Kleinertz & Sven Klimpel & Harry W. Palm Received: 15 July 2011 /Accepted: 4 August 2011 /Published online: 18 August 2011 # Springer-Verlag 2011 Abstract The metazoan parasite fauna and feeding ecology Mollusca, Annelida, Crustacea and Tunicata. The highest of 165 Sprattus sprattus (L., 1758) was studied from number of prey organisms belonged to the crustaceans. The different geographic regions (Baltic Sea, North Sea, English variety of prey items in the stomach was reflected by the Channel, Bay of Biscay, Mediterranean Sea). A total of 13 parasite community differences and parasite species rich- metazoan parasite species were identified including six ness from the different regions. The feeding ecology of the Digenea, one Monogenea, two Cestoda, two Nematoda fish at the sampled localities was responsible for the and two Crustacea. Didymozoidae indet., Lecithocladium observed parasite composition and, secondarily, the zoo- excisum and Bomolochidae indet. represent new host geographical distribution of the parasites, questioning the records. The parasite species richness differed according use of the recorded sprat parasites as biological indicators to regions and ranged between 3 and 10. The most species- for environmental conditions and change. rich parasite fauna was recorded for sprats from the Bay of Biscay (North Atlantic), and the fishes from the Baltic Sea contained the lowest number of parasite species. More Introduction closely connected geographical regions, the North Sea, English Channel and Bay of Biscay, showed more similar Fish parasites are an integral part of every ecosystem and parasite component communities compared with more play an important role for the health of marine organisms.
    [Show full text]
  • A Practical Handbook for Determining the Ages of Gulf of Mexico And
    A Practical Handbook for Determining the Ages of Gulf of Mexico and Atlantic Coast Fishes THIRD EDITION GSMFC No. 300 NOVEMBER 2020 i Gulf States Marine Fisheries Commission Commissioners and Proxies ALABAMA Senator R.L. “Bret” Allain, II Chris Blankenship, Commissioner State Senator District 21 Alabama Department of Conservation Franklin, Louisiana and Natural Resources John Roussel Montgomery, Alabama Zachary, Louisiana Representative Chris Pringle Mobile, Alabama MISSISSIPPI Chris Nelson Joe Spraggins, Executive Director Bon Secour Fisheries, Inc. Mississippi Department of Marine Bon Secour, Alabama Resources Biloxi, Mississippi FLORIDA Read Hendon Eric Sutton, Executive Director USM/Gulf Coast Research Laboratory Florida Fish and Wildlife Ocean Springs, Mississippi Conservation Commission Tallahassee, Florida TEXAS Representative Jay Trumbull Carter Smith, Executive Director Tallahassee, Florida Texas Parks and Wildlife Department Austin, Texas LOUISIANA Doug Boyd Jack Montoucet, Secretary Boerne, Texas Louisiana Department of Wildlife and Fisheries Baton Rouge, Louisiana GSMFC Staff ASMFC Staff Mr. David M. Donaldson Mr. Bob Beal Executive Director Executive Director Mr. Steven J. VanderKooy Mr. Jeffrey Kipp IJF Program Coordinator Stock Assessment Scientist Ms. Debora McIntyre Dr. Kristen Anstead IJF Staff Assistant Fisheries Scientist ii A Practical Handbook for Determining the Ages of Gulf of Mexico and Atlantic Coast Fishes Third Edition Edited by Steve VanderKooy Jessica Carroll Scott Elzey Jessica Gilmore Jeffrey Kipp Gulf States Marine Fisheries Commission 2404 Government St Ocean Springs, MS 39564 and Atlantic States Marine Fisheries Commission 1050 N. Highland Street Suite 200 A-N Arlington, VA 22201 Publication Number 300 November 2020 A publication of the Gulf States Marine Fisheries Commission pursuant to National Oceanic and Atmospheric Administration Award Number NA15NMF4070076 and NA15NMF4720399.
    [Show full text]
  • Do Some Atlantic Bluefin Tuna Skip Spawning?
    SCRS/2006/088 Col. Vol. Sci. Pap. ICCAT, 60(4): 1141-1153 (2007) DO SOME ATLANTIC BLUEFIN TUNA SKIP SPAWNING? David H. Secor1 SUMMARY During the spawning season for Atlantic bluefin tuna, some adults occur outside known spawning centers, suggesting either unknown spawning regions, or fundamental errors in our current understanding of bluefin tuna reproductive schedules. Based upon recent scientific perspectives, skipped spawning (delayed maturation and non-annual spawning) is possibly prevalent in moderately long-lived marine species like bluefin tuna. In principle, skipped spawning represents a trade-off between current and future reproduction. By foregoing reproduction, an individual can incur survival and growth benefits that accrue in deferred reproduction. Across a range of species, skipped reproduction was positively correlated with longevity, but for non-sturgeon species, adults spawned at intervals at least once every two years. A range of types of skipped spawning (constant, younger, older, event skipping; and delays in first maturation) was modeled for the western Atlantic bluefin tuna population to test for their effects on the egg-production-per-recruit biological reference point (stipulated at 20% and 40%). With the exception of extreme delays in maturation, skipped spawning had relatively small effect in depressing fishing mortality (F) threshold values. This was particularly true in comparison to scenarios of a juvenile fishery (ages 4-7), which substantially depressed threshold F values. Indeed, recent F estimates for 1990-2002 western Atlantic bluefin tuna stock assessments were in excess of threshold F values when juvenile size classes were exploited. If western bluefin tuna are currently maturing at an older age than is currently assessed (i.e., 10 v.
    [Show full text]
  • Sturgeons of the Caspian Sea and Ural River
    Photo and image credits: Front Cover: Top left, beluga sturgeon (Huso huso); Top Right: Russian sturgeon (Acipenser gueldenstaedtii); Bottom: stellate sturgeon (Acipenser stellatus); Todd Stailey, Tennessee Aquarium. Back Cover: “FISH IS OUR TREASURE”, Phaedra Doukakis, Ph. D. IOCS; Page 1: Shannon Crownover, The Nature Conservancy; Page 6, 9, 10, 11: Phaedra Doukakis, Ph. D., IOCS; Page 4, 5, 7 designed by Grace Lewis. Brochure content was developed by Alison Ormsby, Ph.D. and Phaedra Doukakis, Ph. D. with editorial review by Yael Wyner, Ph. D. Layout was designed by Grace Lewis. The brochure was developed under a generous grant from Agip KCO. Agip KCO Tel.: international line: 1, K. Smagulov Street +39 02 9138 3300 Atyrau, 06002 Tel: local lines: Republic of Kazakhstan (+7) 7122 92 3300 Fax: (+7) 7122 92 3310 Designed and printed in Kazakhstan www.agipkco.com Sturgeons of the Caspian Sea and Ural River www.oceanconservationscience.org A Unique and Precious Resource What are Sturgeon? River, other rivers off the Caspian Sea are used by sturgeons for With bony plates called scutes on their bodies and ancestors that reproduction, including the Volga River in Russia and the Kura date to the time of dinosaurs, sturgeons are unusual fish. Unlike River in Azerbaijan. However, dams on the Volga and Kura have other types of fish, sturgeons have scutes instead of scales. blocked sturgeons from being able to migrate upriver, and have changed the quality of the rivers so they are no longer able to support sturgeon reproduction. Reproduction: For sturgeon, the process of mixing female eggs and male sperm to create a fertilized egg that hatches into a baby sturgeon.
    [Show full text]
  • Pacific Fisheries
    module 5 PACIFIC FISHERIES 80 MODULE 5 PACIFIC FISHERIES 5.0 FISHERIES IN THE PACIFIC Fish and fishing are culturally and economically critical for most PICTs and are a mainstay of food security in the region. The importance of the fisheries sector to the region’s economy and food security is reflected by its reference in key regional strategies including The Pacific Plan and the Vava’u Declaration on Pacific Fisheries Resources. (See TOOLS 51 & 52.) In the Pacific, a great variety of marine organisms are consumed. In Fiji, for example, over 100 species of finfish and 50 species of invertebrates are officially included in the fish market statistics, and many more species are believed to contribute to the diets of people in rural and urban areas of the Pacific. Fish5 contributes substantially to subsistence and market-based economies and, for some of the smaller PICTs, fishing is their most important renewable resource. Despite growing reliance on imported food products, subsistence fishing still provides the majority of dietary animal protein in the region, and annual per capita consumption of fish ranges from an estimated 13 kg in Papua New Guinea to more than 110 kg in Tuvalu (Table 5.1). According to forecasts of the fish that will be required in 2030 to meet recommended per capita fish consumption in PICTs (34-37 kg/year), or to maintain current consumption levels, coastal fisheries will be able to meet 2030 demand in only 6 of 22 PICTs. Supply is likely to be either marginal or insufficient in the remaining 16 countries, which include the region’s most populous nations of Papua New Guinea, Fiji, Solomon Islands, Samoa and Vanuatu, as shown in Table 5.1.
    [Show full text]
  • J. Mar. Biol. Ass. UK (1958) 37, 7°5-752
    J. mar. biol. Ass. U.K. (1958) 37, 7°5-752 Printed in Great Britain OBSERVATIONS ON LUMINESCENCE IN PELAGIC ANIMALS By J. A. C. NICOL The Plymouth Laboratory (Plate I and Text-figs. 1-19) Luminescence is very common among marine animals, and many species possess highly developed photophores or light-emitting organs. It is probable, therefore, that luminescence plays an important part in the economy of their lives. A few determinations of the spectral composition and intensity of light emitted by marine animals are available (Coblentz & Hughes, 1926; Eymers & van Schouwenburg, 1937; Clarke & Backus, 1956; Kampa & Boden, 1957; Nicol, 1957b, c, 1958a, b). More data of this kind are desirable in order to estimate the visual efficiency of luminescence, distances at which luminescence can be perceived, the contribution it makes to general back• ground illumination, etc. With such information it should be possible to discuss. more profitably such biological problems as the role of luminescence in intraspecific signalling, sex recognition, swarming, and attraction or re• pulsion between species. As a contribution to this field I have measured the intensities of light emitted by some pelagic species of animals. Most of the work to be described in this paper was carried out during cruises of R. V. 'Sarsia' and RRS. 'Discovery II' (Marine Biological Association of the United Kingdom and National Institute of Oceanography, respectively). Collections were made at various stations in the East Atlantic between 30° N. and 48° N. The apparatus for measuring light intensities was calibrated ashore at the Plymouth Laboratory; measurements of animal light were made at sea.
    [Show full text]
  • Spatial and Temporal Distribution of the Demersal Fish Fauna in a Baltic Archipelago As Estimated by SCUBA Census
    MARINE ECOLOGY - PROGRESS SERIES Vol. 23: 3143, 1985 Published April 25 Mar. Ecol. hog. Ser. 1 l Spatial and temporal distribution of the demersal fish fauna in a Baltic archipelago as estimated by SCUBA census B.-0. Jansson, G. Aneer & S. Nellbring Asko Laboratory, Institute of Marine Ecology, University of Stockholm, S-106 91 Stockholm, Sweden ABSTRACT: A quantitative investigation of the demersal fish fauna of a 160 km2 archipelago area in the northern Baltic proper was carried out by SCUBA census technique. Thirty-four stations covering seaweed areas, shallow soft bottoms with seagrass and pond weeds, and deeper, naked soft bottoms down to a depth of 21 m were visited at all seasons. The results are compared with those obtained by traditional gill-net fishing. The dominating species are the gobiids (particularly Pornatoschistus rninutus) which make up 75 % of the total fish fauna but only 8.4 % of the total biomass. Zoarces viviparus, Cottus gobio and Platichtys flesus are common elements, with P. flesus constituting more than half of the biomass. Low abundance of all species except Z. viviparus is found in March-April, gobies having a maximum in September-October and P. flesus in November. Spatially, P. rninutus shows the widest vertical range being about equally distributed between surface and 20 m depth. C. gobio aggregates in the upper 10 m. The Mytilus bottoms and the deeper soft bottoms are the most populated areas. The former is characterized by Gobius niger, Z. viviparus and Pholis gunnellus which use the shelter offered by the numerous boulders and stones. The latter is totally dominated by P.
    [Show full text]
  • First Record of a Coregonid Fish Species, Coregenus Albula (Linnaeus, 1758) (Salmoniformes: Salmonidae) in Aktaş Lake Shared Between Turkey and Georgia
    J. Black Sea/Mediterranean Environment Vol. 25, No. 3: 325-332 (2019) SHORT COMMUNICATION First record of a coregonid fish species, Coregenus albula (Linnaeus, 1758) (Salmoniformes: Salmonidae) in Aktaş Lake shared between Turkey and Georgia Sedat V. Yerli Department of Biology, Hacettepe University, SAL, Beytepe, Ankara, TURKEY Corresponding author: [email protected] Abstract The genus Coregenus (Salmoniformes: Salmonidae) was recently considered not to be represented in Turkey. European cisco or vendace, Coregonus albula (Linnaeus, 1758) was reported for the first time for Turkey in this article with fifteen samples in Aktaş Lake, Ardahan. This species should be added to the checklist of Turkish fish fauna. Turkish name is proposed as “Akbalık” for this species. Keywords: Coregonus albula, first record, Aktaş Lake, Kartsakhi, alkaline lake, Georgia, Turkey Received: 30.10.2019, Accepted: 26.11.2019 Vendace or European cisco Coregonus albula (Linnaeus, 1758) is a native species for northern Europe. Berg (1948) reported the distribution of this species its morphological measurements in the former USSR and adjacent countries. Froese and Pauly (2019) summarized the natural distribution of vendace as Baltic basin, several lakes of upper Volga drainage; some lakes of White Sea basin and North Sea basin east of Elbe drainage; anadromous in Gulf of Finland and marine in northernmost freshened part of Gulf of Bothnia between Finland and Sweden; in Lake Inari, northern Finland; lower Rhine (now extirpated). The vendace was introduced, intentionally in some countries in Europe and United States of America. Vendace was introduced in 1959, 1982-1987 in the Irtysh River Basin and in 1960-61 in Lake Balkhash in Kazakhstan (Mitrofanov and Petr 1999).
    [Show full text]
  • In the Kattegat and Skagerrak, Eastern North Sea
    Aquat. Living Resour. 28, 127–137 (2015) Aquatic c EDP Sciences 2016 DOI: 10.1051/alr/2016007 Living www.alr-journal.org Resources Growth and maturity of sprat (Sprattus sprattus) in the Kattegat and Skagerrak, eastern North Sea Francesca Vitale1, Felix Mittermayer1,2, Birgitta Krischansson1, Marianne Johansson1 and Michele Casini1,a 1 Swedish University of Agricultural Sciences, Department of Aquatic Resources, Institute of Marine Research, 45330 Lysekil, Sweden 2 GEOMAR Helmholtz Centre for Ocean Research, Evolutionary Ecology of Marine Fishes, 24105 Kiel, Germany Received 13 July 2015; Accepted 12 February 2016 Abstract – Information on fish biology, as growth and reproduction, is an essential first step for a sound assessment and management of a fishery resource. Here we analyzed the annual cycle of body condition factor (K), gonadosomatic index (GSI) and maturity of sprat from the Skagerrak and Kattegat as well as from the Skagerrak inner fjords (Uddevalla fjords). The results show an inverse yearly pattern for K and GSI in both areas, K being the highest in autumn and lowest in spring, while the GSI index was highest in spring and lowest in autumn. The annual highest proportion of spawning fish was recorded from May to July, indicating the late spring and early summer as the main spawning period for sprat in these areas. Male sprat reached maturity at a higher size in the Uddevalla fjords compared to Skagerrak and Kattegat, while negligible differences were shown by females. The K, GSI and size-at-age were the lowest in the Uddevalla fjords, while K and GSI were the highest in the Skagerrak, potentially related to the different environmental conditions encountered in the different areas.
    [Show full text]
  • A Preliminary Study on the Stomach Content of Southern Bluefin Tuna Thunnus Maccoyii Caught by Taiwanese Longliner in the Central Indian Ocean
    CCSBT-ESC/0509/35 A preliminary study on the stomach content of southern bluefin tuna Thunnus maccoyii caught by Taiwanese longliner in the central Indian Ocean Kwang-Ming Liu1, Wei-Ke Chen2, Shoou-Jeng Joung2, and Sui-Kai Chang3 1. Institute of Marine Resource Management, National Taiwan Ocean University, Keelung, Taiwan. 2. Department of Environmental Biology and Fisheries Science, National Taiwan Ocean University, Keelung, Taiwan. 3. Fisheries Agency, Council of Agriculture, Taipei, Taiwan. Abstract The stomach contents of 63 southern bluefin tuna captured by Taiwanese longliners in central Indian Ocean in August 2004 were examined. The size of tunas ranged from 84-187 cm FL (12-115 kg GG). The length and weight frequency distributions indicated that most specimens were in the range of 100-130 cm FL with a body weight between 10 and 30 kg for both sexes. The sexes- combined relationship between dressed weight and fork length can be described by W = 6.975× 10-6× FL3.1765 (n=56, r2=0.967, p < 0.05). The subjective index of fullness of specimens was estimated as: 1 = empty (38.6%), 2 = <half full (47.37%), 3 = half full (3.51%), 4 = >half full (5.26%), and 5 = full (5.26%). For the stomachs with prey items, almost all the preys are pisces and the proportion of each prey groups are fishes (95.6%), cephalopods (2.05%), and crustaceans (0.02%). In total, 6 prey taxa were identified – 4 species of fish, 1 unidentified pisces, 1 unidentified crustacean, and 1 unidentified squid. The 4 fish species fall in the family of Carangidae, Clupeidae, Emmelichthyidae, and Hemiramphidae.
    [Show full text]
  • THE CASE AGAINST Marine Mammals in Captivity Authors: Naomi A
    s l a m m a y t T i M S N v I i A e G t A n i p E S r a A C a C E H n T M i THE CASE AGAINST Marine Mammals in Captivity The Humane Society of the United State s/ World Society for the Protection of Animals 2009 1 1 1 2 0 A M , n o t s o g B r o . 1 a 0 s 2 u - e a t i p s u S w , t e e r t S h t u o S 9 8 THE CASE AGAINST Marine Mammals in Captivity Authors: Naomi A. Rose, E.C.M. Parsons, and Richard Farinato, 4th edition Editors: Naomi A. Rose and Debra Firmani, 4th edition ©2009 The Humane Society of the United States and the World Society for the Protection of Animals. All rights reserved. ©2008 The HSUS. All rights reserved. Printed on recycled paper, acid free and elemental chlorine free, with soy-based ink. Cover: ©iStockphoto.com/Ying Ying Wong Overview n the debate over marine mammals in captivity, the of the natural environment. The truth is that marine mammals have evolved physically and behaviorally to survive these rigors. public display industry maintains that marine mammal For example, nearly every kind of marine mammal, from sea lion Iexhibits serve a valuable conservation function, people to dolphin, travels large distances daily in a search for food. In learn important information from seeing live animals, and captivity, natural feeding and foraging patterns are completely lost.
    [Show full text]
  • Age, Growth and Reproductive Period of White Bream, Blicca Bjoerkna (L., 1758) in Lake Ladik, Turkey
    LIMNOFISH-Journal of Limnology and Freshwater Fisheries Research 1(1): 9-18 (2015) Age, Growth and Reproductive Period of White Bream, Blicca bjoerkna (L., 1758) in Lake Ladik, Turkey Savaş YILMAZ1,*, Okan YAZICIOĞLU2, Ramazan YAZICI3, Nazmi POLAT1 1 Ondokuz Mayıs University, Faculty of Arts and Science, Department of Biology, Samsun-Turkey 2 Ahi Evran University, Technical Vocational Schools of Higher Education, Botanic and Animal Production Department, Organic Farming Program, Kırşehir-Turkey 3 Ahi Evran University, Çiçekdağı Technical Vocational Schools of Higher Education, Laboratory and Veterinary Health Department, Kırşehir-Turkey ABSTRACT ARTICLE INFO The white bream, Blicca bjoerkna (L., 1758) specimens (n=434) were collected RESEARCH ARTICLE from Lake Ladik between November 2009 and October 2010 in order to determine the age, growth, and reproductive season. Fork lengths and weights of Received : 08.01.2015 these samples varied between 11.5-24.3 cm and 22.80-259.00 g, respectively. Age Revised : 16.03.2015 estimates obtained from scales and vertebrae were compared to determine the most reliable bony structure for ageing. The precision analyses indicated that Accepted : 17.03.2015 scales were the most appropriate hard structures for determining the age of white Published : 20.04.2015 bream. Ages of all the specimens ranged from I to VI years and age group III was dominant. The parameters of the von Bertalanffy growth equations were -1 calculated as L∞ = 32.85 cm, W∞ = 707.76 g, k = 0.11 year and t0 = -2.64 year, and the growth performance index (Φ') value was computed as 2.074 for * CORRESPONDING AUTHOR combined sexes.
    [Show full text]