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Comparison of the Myxobolus Fauna of Common Barbel from Hungary and Iberian Barbel from Portugal
Vol. 100: 231–248, 2012 DISEASES OF AQUATIC ORGANISMS Published September 12 doi: 10.3354/dao02469 Dis Aquat Org Comparison of the Myxobolus fauna of common barbel from Hungary and Iberian barbel from Portugal K. Molnár1,*, E. Eszterbauer1, Sz. Marton1, Cs. Székely1, J. C. Eiras2 1Institute for Veterinary Medical Research, Centre for Agricultural Research, HAS, POB 18, 1581 Budapest, Hungary 2Departamento de Biologia, e CIIMAR, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre, s/n, Edifício FC4, 4169-007 Porto, Portugal ABSTRACT: We compared Myxobolus infection of common barbel Barbus barbus from the Danube River in Hungary with that in Iberian barbel Luciobarbus bocagei from the Este River in Portugal. In Hungary, we recorded 5 known Myxobolus species (M. branchialis, M. caudatus, M. musculi, M. squamae, and M. tauricus) and described M. branchilateralis sp. n. In Portugal we recorded 6 Myxobolus species (M. branchialis, M. branchilateralis sp. n., M. cutanei, M. musculi, M. pfeifferi, and M. tauricus). Species found in the 2 habitats had similar spore morphology and only slight differences were observed in spore shape or measurements. All species showed a spe- cific tissue tropism and had a definite site selection. M. branchialis was recorded from the lamellae of the gills, large plasmodia of M. branchilateralis sp. n. developed at both sides of hemibranchia, M. squamae infected the scales, plasmodia of M. caudatus infected the scales and the fins, and M. tauricus were found in the fins and pin bones. In the muscle, 3 species, M. musculi, M. pfeifferi and M. tauricus were found; however they were found in distinct locations. -
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. -
FIELD GUIDE to WARMWATER FISH DISEASES in CENTRAL and EASTERN EUROPE, the CAUCASUS and CENTRAL ASIA Cover Photographs: Courtesy of Kálmán Molnár and Csaba Székely
SEC/C1182 (En) FAO Fisheries and Aquaculture Circular I SSN 2070-6065 FIELD GUIDE TO WARMWATER FISH DISEASES IN CENTRAL AND EASTERN EUROPE, THE CAUCASUS AND CENTRAL ASIA Cover photographs: Courtesy of Kálmán Molnár and Csaba Székely. FAO Fisheries and Aquaculture Circular No. 1182 SEC/C1182 (En) FIELD GUIDE TO WARMWATER FISH DISEASES IN CENTRAL AND EASTERN EUROPE, THE CAUCASUS AND CENTRAL ASIA By Kálmán Molnár1, Csaba Székely1 and Mária Láng2 1Institute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary 2 National Food Chain Safety Office – Veterinary Diagnostic Directorate, Budapest, Hungary FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS Ankara, 2019 Required citation: Molnár, K., Székely, C. and Láng, M. 2019. Field guide to the control of warmwater fish diseases in Central and Eastern Europe, the Caucasus and Central Asia. FAO Fisheries and Aquaculture Circular No.1182. Ankara, FAO. 124 pp. Licence: CC BY-NC-SA 3.0 IGO The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations (FAO) concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of specific companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO in preference to others of a similar nature that are not mentioned. The views expressed in this information product are those of the author(s) and do not necessarily reflect the views or policies of FAO. -
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. -
IATTC-94-01 the Tuna Fishery, Stocks, and Ecosystem in the Eastern
INTER-AMERICAN TROPICAL TUNA COMMISSION 94TH MEETING Bilbao, Spain 22-26 July 2019 DOCUMENT IATTC-94-01 REPORT ON THE TUNA FISHERY, STOCKS, AND ECOSYSTEM IN THE EASTERN PACIFIC OCEAN IN 2018 A. The fishery for tunas and billfishes in the eastern Pacific Ocean ....................................................... 3 B. Yellowfin tuna ................................................................................................................................... 50 C. Skipjack tuna ..................................................................................................................................... 58 D. Bigeye tuna ........................................................................................................................................ 64 E. Pacific bluefin tuna ............................................................................................................................ 72 F. Albacore tuna .................................................................................................................................... 76 G. Swordfish ........................................................................................................................................... 82 H. Blue marlin ........................................................................................................................................ 85 I. Striped marlin .................................................................................................................................... 86 J. Sailfish -
Spawning of Bluefin Tuna in the Black Sea: Historical Evidence, Environmental Constraints and Population Plasticity
CORE Downloaded from orbit.dtu.dk on: Dec 20, 2017 Metadata, citation and similar papers at core.ac.uk Provided by Online Research Database In Technology Spawning of bluefin tuna in the black sea: historical evidence, environmental constraints and population plasticity MacKenzie, Brian; Mariani, Patrizio Published in: PLoS ONE Link to article, DOI: 10.1371/journal.pone.0039998 Publication date: 2012 Document Version Publisher's PDF, also known as Version of record Link back to DTU Orbit Citation (APA): Mackenzie, B. R., & Mariani, P. (2012). Spawning of bluefin tuna in the black sea: historical evidence, environmental constraints and population plasticity. PLoS ONE, 7(7), e39998. DOI: 10.1371/journal.pone.0039998 General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Spawning of Bluefin Tuna in the Black Sea: Historical Evidence, -
FIELD GUIDE to WARMWATER FISH DISEASES in CENTRAL and EASTERN EUROPE, the CAUCASUS and CENTRAL ASIA Cover Photographs: Courtesy of Kálmán Molnár and Csaba Székely
SEC/C1182 (En) FAO Fisheries and Aquaculture Circular I SSN 2070-6065 FIELD GUIDE TO WARMWATER FISH DISEASES IN CENTRAL AND EASTERN EUROPE, THE CAUCASUS AND CENTRAL ASIA Cover photographs: Courtesy of Kálmán Molnár and Csaba Székely. FAO Fisheries and Aquaculture Circular No. 1182 SEC/C1182 (En) FIELD GUIDE TO WARMWATER FISH DISEASES IN CENTRAL AND EASTERN EUROPE, THE CAUCASUS AND CENTRAL ASIA By Kálmán Molnár1, Csaba Székely1 and Mária Láng2 1Institute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary 2 National Food Chain Safety Office – Veterinary Diagnostic Directorate, Budapest, Hungary FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS Ankara, 2019 Required citation: Molnár, K., Székely, C. and Láng, M. 2019. Field guide to the control of warmwater fish diseases in Central and Eastern Europe, the Caucasus and Central Asia. FAO Fisheries and Aquaculture Circular No.1182. Ankara, FAO. 124 pp. Licence: CC BY-NC-SA 3.0 IGO The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations (FAO) concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of specific companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO in preference to others of a similar nature that are not mentioned. The views expressed in this information product are those of the author(s) and do not necessarily reflect the views or policies of FAO. -
Changing Communities of Baltic Coastal Fish Executive Summary: Assessment of Coastal fi Sh in the Baltic Sea
Baltic Sea Environment Proceedings No. 103 B Changing Communities of Baltic Coastal Fish Executive summary: Assessment of coastal fi sh in the Baltic Sea Helsinki Commission Baltic Marine Environment Protection Commission Baltic Sea Environment Proceedings No. 103 B Changing Communities of Baltic Coastal Fish Executive summary: Assessment of coastal fi sh in the Baltic Sea Helsinki Commission Baltic Marine Environment Protection Commission Editor: Janet Pawlak Authors: Kaj Ådjers (Co-ordination Organ for Baltic Reference Areas) Jan Andersson (Swedish Board of Fisheries) Magnus Appelberg (Swedish Board of Fisheries) Redik Eschbaum (Estonian Marine Institute) Ronald Fricke (State Museum of Natural History, Stuttgart, Germany) Antti Lappalainen (Finnish Game and Fisheries Research Institute), Atis Minde (Latvian Fish Resources Agency) Henn Ojaveer (Estonian Marine Institute) Wojciech Pelczarski (Sea Fisheries Institute, Poland) Rimantas Repečka (Institute of Ecology, Lithuania). Photographers: Visa Hietalahti p. cover, 7 top, 8 bottom Johnny Jensen p. 3 top, 3 bottom, 4 middle, 4 bottom, 5 top, 8 top, 9 top, 9 bottom Lauri Urho p. 4 top, 5 bottom Juhani Vaittinen p. 7 bottom Markku Varjo / LKA p. 10 top For bibliographic purposes this document should be cited as: HELCOM, 2006 Changing Communities of Baltic Coastal Fish Executive summary: Assessment of coastal fi sh in the Baltic Sea Balt. Sea Environ. Proc. No. 103 B 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 - Design and layout: Bitdesign, Vantaa, Finland Printed by: Erweko Painotuote Oy, Finland ISSN 0357-2994 Coastal fi sh – a combination of freshwater and marine species Coastal fish communities are important components of Baltic Sea ecosystems. -
Sprat Sprattus Sprattus Max Size: 16 Cm Family Clupeidae Max Age: 5 Years
Sprat Sprattus sprattus Max size: 16 cm Family Clupeidae Max age: 5 years Introduction Taxonomy: European sprat Sprattus sprattus (Linnaeus, 1758) (Order: Clupeiformes, Family: Clupeidae) is one of five clupeids occurring in the North Sea. Three sub-species have been defined [1], namely S. sprattus sprattus in the North-East Atlantic and North Sea, S. sprattus balticus in the Baltic Sea and S. sprattus phalericus in the Mediterranean and Black Seas. Comm. common names Danish Brisling Icelandic Brislingur Dutch Sprot Latvian Bt tli a English Sprat Norwegian Brisling Estonian Kilu Polish Szprot Faroese Brislingur Portuguese Espadilha / Lavadilha Finnish Kilohaili Russian French Sprat Spanish Espadín German Sprott Swedish Skarpsill General: Sprat is a small-bodied pelagic schooling species that is most abundant in relatively shallow waters, including areas of low salinity such as the Baltic. It is an important food resource for many top predators. Sprat is mainly landed for industrial processing (often mixed with juvenile herring), but a small market exists for human consumption (smoked sprat and whitebait). Sprat may be confused with juvenile herring, but the relative positions of dorsal and pelvic fins, the grey rather than blue coloration on the dorsal side and the sharply toothed keel on the belly are clear distinguishing features. Minimum Landing Size: None. Distribution Biogeographical distribution: Sprat is widely distributed in the shelf waters of Europe and North Africa, ranging from Morocco to Norway, including the Mediterranean, Black Sea and Baltic Sea [1,2], but stays largely within the 50 m depth contour and is also common in inshore waters. Spatial distribution in North Sea: Sprat is most abundant south of the Dogger Bank and in the Kattegat (Fig. -
Spawning of Bluefin Tuna in the Black Sea: Historical Evidence, Environmental Constraints and Population Plasticity
Spawning of Bluefin Tuna in the Black Sea: Historical Evidence, Environmental Constraints and Population Plasticity Brian R. MacKenzie1*, Patrizio Mariani2 1 Center for Macroecology, Evolution and Climate, National Institute for Aquatic Resources (DTU Aqua), Technical University of Denmark, Charlottenlund, Denmark, 2 Center for Ocean Life, National Institute for Aquatic Resources (DTU Aqua), Technical University of Denmark, Charlottenlund, Denmark Abstract The lucrative and highly migratory Atlantic bluefin tuna, Thunnus thynnus (Linnaeus 1758; Scombridae), used to be distributed widely throughout the north Atlantic Ocean, Mediterranean Sea and Black Sea. Its migrations have supported sustainable fisheries and impacted local cultures since antiquity, but its biogeographic range has contracted since the 1950s. Most recently, the species disappeared from the Black Sea in the late 1980s and has not yet recovered. Reasons for the Black Sea disappearance, and the species-wide range contraction, are unclear. However bluefin tuna formerly foraged and possibly spawned in the Black Sea. Loss of a locally-reproducing population would represent a decline in population richness, and an increase in species vulnerability to perturbations such as exploitation and environmental change. Here we identify the main genetic and phenotypic adaptations that the population must have (had) in order to reproduce successfully in the specific hydrographic (estuarine) conditions of the Black Sea. By comparing hydrographic conditions in spawning areas of the three species of bluefin tunas, and applying a mechanistic model of egg buoyancy and sinking rate, we show that reproduction in the Black Sea must have required specific adaptations of egg buoyancy, fertilisation and development for reproductive success. Such adaptations by local populations of marine fish species spawning in estuarine areas are common as is evident from a meta-analysis of egg buoyancy data from 16 species of fish. -
How Barriers Shape Freshwater Fish Distributions: a Species Distribution Model Approach
1 How barriers shape freshwater fish distributions: a species distribution model approach 2 3 Mathias Kuemmerlen1* [email protected] 4 Stefan Stoll1,2 [email protected] 5 Peter Haase1,3 [email protected] 6 7 1Senckenberg Research Institute and Natural History Museum Frankfurt, Department of River 8 Ecology and Conservation, Clamecystr. 12, D-63571 Gelnhausen, Germany 9 2University of Koblenz-Landau, Institute for Environmental Sciences, Fortstr. 7, 76829 Landau, 10 Germany 11 3University of Duisburg-Essen, Faculty of Biology, Essen, Germany 12 *Corresponding author: Tel: +49 6051-61954-3120 13 Fax: +49 6051-61954-3118 14 15 Running title: How barriers shape fish distributions 16 17 Word count main text = 4679 18 1 PeerJ Preprints | https://doi.org/10.7287/peerj.preprints.2112v2 | CC BY 4.0 Open Access | rec: 18 Aug 2016, publ: 18 Aug 2016 19 Abstract 20 Aim 21 Barriers continue to be built globally despite their well-known negative effects on freshwater 22 ecosystems. Fish habitats are disturbed by barriers and the connectivity in the stream network 23 reduced. We implemented and assessed the use of barrier data, including their size and 24 magnitude, in distribution predictions for 20 species of freshwater fish to understand the 25 impacts on freshwater fish distributions. 26 27 Location 28 Central Germany 29 30 Methods 31 Obstruction metrics were calculated from barrier data in three different spatial contexts 32 relevant to fish migration and dispersal: upstream, downstream and along 10km of stream 33 network. The metrics were included in a species distribution model and compared to a model 34 without them, to reveal how barriers influence the distribution patterns of fish species. -
Divovich-Et-Al-Russia-Black-Sea.Pdf
Fisheries Centre The University of British Columbia Working Paper Series Working Paper #2015 - 84 Caviar and politics: A reconstruction of Russia’s marine fisheries in the Black Sea and Sea of Azov from 1950 to 2010 Esther Divovich, Boris Jovanović, Kyrstn Zylich, Sarah Harper, Dirk Zeller and Daniel Pauly Year: 2015 Email: [email protected] This working paper is available by the Fisheries Centre, University of British Columbia, Vancouver, BC, V6T made 1Z4, Canada. CAVIAR AND POLITICS: A RECONSTRUCTION OF RUSSIA’S MARINE FISHERIES IN THE BLACK SEA AND SEA OF AZOV FROM 1950 TO 2010 Esther Divovich, Boris Jovanović, Kyrstn Zylich, Sarah Harper, Dirk Zeller and Daniel Pauly Sea Around Us, Fisheries Centre, University of British Columbia, 2202 Main Mall, Vancouver, V6T 1Z4, Canada Corresponding author : [email protected] ABSTRACT The aim of the present study was to reconstruct total Russian fisheries catch in the Black Sea and Sea of Azov for the period 1950 to 2010. Using catches presented by FAO on behalf of the USSR and Russian Federation as a baseline, total removals were estimated by adding estimates of unreported commercial catches, discards at sea, and unreported recreational and subsistence catches. Estimates for ‘ghost fishing’ were also made, but not included in the final reconstructed catch. Total removals by Russia were estimated to be 1.57 times the landings presented by FAO (taking into account USSR-disaggregation), with unreported commercial catches, discards, recreational, and subsistence fisheries representing an additional 30.6 %, 24.7 %, 1.0%, and 0.7 %, respectively. Discards reached their peak in the 1970s and 1980s during a period of intense bottom trawling for sprat that partially contributed to the large-scale fisheries collapse in the 1990s.