Field Guide to the Living Marine Resources of Namibia.Pdf
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An Eclectic Overview of the SA Marine Science Community
A biologists’ personal overview of the SA Marine Science community and its outputs (2001-2006)*1 Mark J Gibbons, Department of Biodiversity and Conservation Biology, University of the Western Cape, Private Bag X17, Bellville 7535, South Africa. Email: [email protected] ABSTRACT I have analysed 1 295 of the outputs published by the South African Marine Science Community (SAMSC) in either peer-reviewed journals or as books/book chapters for the period 2001-2006, with a view to identifying trends in the field, summarizing institutional overlaps and assessing the demographic state-of-play. Although almost 70% of our outputs were published internationally, we published the bulk of our research in strictly marine science journals which suggests, perhaps, that we need to be thinking bigger. More than 22% of all outputs were led by International colleagues, and these were published in journals with a significantly higher Impact Factor than those led by local authors. Women led less than 25%, and persons from previously disadvantaged backgrounds led less than 10%, of all outputs: this needs monitoring, discussion and pro-active response by employers. Thirty-six authors (~95% male, ~97% white) were responsible for more than 50% of all outputs, which suggests that the field is not totally dominated by an ageing cohort. Despite the fact that the bulk of the SAMSC is centred in the SW Cape, our study areas are approximately equally spread around the coastline, though there is an obvious institutional bias to the geographical location of study sites. Globally-orientated studies were generally published in “better” outlets than locally-orientated work, and were more likely to be led by international colleagues. -
Jubilee Field Draft EIA Chapter 4 6 Aug 09.Pdf
4 ENVIRONMENTAL AND SOCIO-ECONOMIC BASELINE 4.1 INTRODUCTION This chapter provides a description of the current environmental and socio- economic situation against which the potential impacts of the Jubilee Field Phase 1 development can be assessed and future changes monitored. The chapter presents an overview of the aspects of the environment relating to the surrounding area in which the Jubilee Field Phase 1 development will take place and which may be directly or indirectly affected by the proposed project. This includes the Jubilee Unit Area, the Ghana marine environment at a wider scale and the six districts of the Western Region bordering the marine environment. The Jubilee Unit Area and its regional setting are shown in Figure 4.1. The project area is approximately 132 km west-southwest of the city of Takoradi, 60 km from the nearest shoreline of Ghana, and 75 km from the nearest shoreline of Côte d’Ivoire. Figure 4.1 Project Location and Regional Setting ENVIRONMENTAL RESOURCES MANAGEMENT TULLOW GHANA LIMITED 4-1 The baseline description draws on a number of primary and secondary data sources. Primary data sources include recent hydrographic studies undertaken as part of the exploration well drilling programme in the Jubilee field area, as well as an Environmental Baseline Survey (EBS) which was commissioned by Tullow and undertaken by TDI Brooks (2008). An electronic copy of the EBS is attached to this EIS. It is noted that information on the offshore distribution and ecology of marine mammals, turtles and offshore pelagic fish is more limited due to limited historic research in offshore areas. -
Nocturnal Feeding of Pacific Hake and Jack Mackerel Off the Mouth of the Columbia River, 1998-2004: Implications for Juvenile Salmon Predation Robert L
This article was downloaded by: [Oregon State University] On: 16 August 2011, At: 13:01 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Transactions of the American Fisheries Society Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/utaf20 Nocturnal Feeding of Pacific Hake and Jack Mackerel off the Mouth of the Columbia River, 1998-2004: Implications for Juvenile Salmon Predation Robert L. Emmett a & Gregory K. Krutzikowsky b a Northwest Fisheries Science Center, NOAA Fisheries, 2030 South Marine Science Drive, Newport, Oregon, 97365, USA b Cooperative Institute of Marine Resource Studies, Oregon State University, 2030 South Marine Science Drive, Newport, Oregon, 97365, USA Available online: 09 Jan 2011 To cite this article: Robert L. Emmett & Gregory K. Krutzikowsky (2008): Nocturnal Feeding of Pacific Hake and Jack Mackerel off the Mouth of the Columbia River, 1998-2004: Implications for Juvenile Salmon Predation, Transactions of the American Fisheries Society, 137:3, 657-676 To link to this article: http://dx.doi.org/10.1577/T06-058.1 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.tandfonline.com/page/terms-and- conditions This article may be used for research, teaching and private study purposes. Any substantial or systematic reproduction, re-distribution, re-selling, loan, sub-licensing, systematic supply or distribution in any form to anyone is expressly forbidden. The publisher does not give any warranty express or implied or make any representation that the contents will be complete or accurate or up to date. -
Simulations of Fishing Effects on the Southern Benguela Fish Community Using an Individual-Based Model: Learning from a Comparison with Ecosim
Ecosystem Approaches to Fisheries in the Southern Benguela Afr. J. mar. Sci. 26: 95–114 2004 95 SIMULATIONS OF FISHING EFFECTS ON THE SOUTHERN BENGUELA FISH COMMUNITY USING AN INDIVIDUAL-BASED MODEL: LEARNING FROM A COMPARISON WITH ECOSIM Y-J. SHIN*, L. J. SHANNON† and P. M. CURY* By applying an individual-based model (OSMOSE) to the southern Benguela ecosystem, a multispecies analysis is proposed, complementary to that provided by the application of ECOPATH/ECOSIM models. To reconstruct marine foodwebs, OSMOSE is based on the hypothesis that predation is a size-structured process. In all, 12 fish species, chosen for their importance in terms of biomass and catches, are explicitly modelled. Growth, repro- duction and mortality parameters are required to model their dynamics and trophic interactions. Maps of mean spatial distribution of the species are compiled from published literature. Taking into account the spatial component is necessary because spatial co-occurrence determines potential interactions between predatory fish and prey fish of suitable size. To explore ecosystem effects of fishing, different fishing scenarios, previously examined using ECOSIM, are simulated using the OSMOSE model. They explore the effects of targeting fish species in the southern Benguela considered to be predators (Cape hake Merluccius capensis and M. paradoxus) or prey (anchovy Engraulis encrasicolus, sardine Sardinops sagax, round herring Etrumeus whiteheadi). Simulation results are compared and are generally consistent with those obtained using an ECOSIM model. This cross-validation appears to be a promising means of evaluating the robustness of model outputs, when separate validation of marine ecosystem models are still difficult to perform. -
Monthly Highlights
Monthly Highlights No. 2 / 2021 In this issue As of 2021, the Monthly Highlights include Bulgaria among surveyed countries. According to data collected by EUMOFA from 13 EU Member States, in November 2020 striped venus and whelk together accounted for 12% of the total Contents first-sales value of the “Bivalves and other molluscs and aquatic invertebrates” commodity group. First sales in Europe Striped venus (Italy, Spain) and whelk From 2018 to 2020, the price of live, fresh, or chilled (Belgium, France, Netherlands) mussels imported in the EU from Norway fluctuated from 2,04 to 7,09 EUR/kg. In 2020, both price and Extra-EU imports volume exhibited a downward trend. Weekly average EU import prices of selected products from Over the last four years, German consumers spent selected countries of origin the most for a kilogram of fresh cod, (18,00 EUR/kg on average) compared to France Consumption Fresh cod in Germany, France, and the (16,80 EUR/kg) and the Netherlands (16,30 EUR/kg). Netherlands In 2019, the EU imports of fisheries and aquaculture products from South Africa accounted for over EUR Case studies 295 million and 80.597 tonnes. Hake, squid, and Fisheries and aquaculture in South Africa fishmeal constitute the bulk share of EU imports. Horse mackerel in the EU The largest market for horse mackerel exported by the EU is Egypt. In 2019, exports to the country Global highlights reached 54.000 tonnes, worth EUR 51 million, accounting for 50% of total export volume Macroeconomic context and 47% of value. Marine fuel, consumer prices, and In January 2021, the EU and Greenland concluded exchange rates negotiations for a new four-year Sustainable Fisheries Partnership Agreement (SFPA), which is the third most important agreement in place for the EU in financial terms. -
Updated Checklist of Marine Fishes (Chordata: Craniata) from Portugal and the Proposed Extension of the Portuguese Continental Shelf
European Journal of Taxonomy 73: 1-73 ISSN 2118-9773 http://dx.doi.org/10.5852/ejt.2014.73 www.europeanjournaloftaxonomy.eu 2014 · Carneiro M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:9A5F217D-8E7B-448A-9CAB-2CCC9CC6F857 Updated checklist of marine fishes (Chordata: Craniata) from Portugal and the proposed extension of the Portuguese continental shelf Miguel CARNEIRO1,5, Rogélia MARTINS2,6, Monica LANDI*,3,7 & Filipe O. COSTA4,8 1,2 DIV-RP (Modelling and Management Fishery Resources Division), Instituto Português do Mar e da Atmosfera, Av. Brasilia 1449-006 Lisboa, Portugal. E-mail: [email protected], [email protected] 3,4 CBMA (Centre of Molecular and Environmental Biology), Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. E-mail: [email protected], [email protected] * corresponding author: [email protected] 5 urn:lsid:zoobank.org:author:90A98A50-327E-4648-9DCE-75709C7A2472 6 urn:lsid:zoobank.org:author:1EB6DE00-9E91-407C-B7C4-34F31F29FD88 7 urn:lsid:zoobank.org:author:6D3AC760-77F2-4CFA-B5C7-665CB07F4CEB 8 urn:lsid:zoobank.org:author:48E53CF3-71C8-403C-BECD-10B20B3C15B4 Abstract. The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. -
TNP SOK 2011 Internet
GARDEN ROUTE NATIONAL PARK : THE TSITSIKAMMA SANP ARKS SECTION STATE OF KNOWLEDGE Contributors: N. Hanekom 1, R.M. Randall 1, D. Bower, A. Riley 2 and N. Kruger 1 1 SANParks Scientific Services, Garden Route (Rondevlei Office), PO Box 176, Sedgefield, 6573 2 Knysna National Lakes Area, P.O. Box 314, Knysna, 6570 Most recent update: 10 May 2012 Disclaimer This report has been produced by SANParks to summarise information available on a specific conservation area. Production of the report, in either hard copy or electronic format, does not signify that: the referenced information necessarily reflect the views and policies of SANParks; the referenced information is either correct or accurate; SANParks retains copies of the referenced documents; SANParks will provide second parties with copies of the referenced documents. This standpoint has the premise that (i) reproduction of copywrited material is illegal, (ii) copying of unpublished reports and data produced by an external scientist without the author’s permission is unethical, and (iii) dissemination of unreviewed data or draft documentation is potentially misleading and hence illogical. This report should be cited as: Hanekom N., Randall R.M., Bower, D., Riley, A. & Kruger, N. 2012. Garden Route National Park: The Tsitsikamma Section – State of Knowledge. South African National Parks. TABLE OF CONTENTS 1. INTRODUCTION ...............................................................................................................2 2. ACCOUNT OF AREA........................................................................................................2 -
An Annotated Checklist of Philippine Flatfish: Ecological Implications3'
An Annotated Checklist of Philippine Flatfish: Ecological Implications3' A. Cabanbanb) E. Capulic) R. Froesec) and D. Pauly1" Abstract An annotated list of the flatfish of the Philippines was assembled, covering 108 species (vs. 74 in the entire North Atlantic), and thus highlighting this country's feature of being at the center of the world's marine biodiversity. More than 80 recent references relating to Philippine flatfish are assembled. Various biological inferences are drawn from the small sizes typical of Philippine (and tropical) flatfish, and pertinent to the "systems dynamics of flatfish". This was facilitated by the FishBase CD-ROM, which documents all data presented here, and which was used to generate the graphs supporting these biological inferences. a) For presentation at the Third International Symposium on Flatfish Ecology, 2-8 November 1996, Netherlands Institute for Sea Research (NIOZ), Texel, The Netherlands. ICLARM Contribution No. 1321. b> Borneo Marine Research Unit, Universiti Malaysia Sabah, 9th Floor Gaya Centre, Jalan Tun Fuad Stephens, Locked Bag 2073, 88999 Kota Kinabalu, Sabah, Malaysia. c) International Center for Living Aquatic Resources Management (ICLARM), MCPO Box 2631, 0718 Makati City, Philippines. d) Fisheries Centre, University of British Columbia, 2204 Main Mall, Vancouver, B.C. Canada V6T 1Z4. E- mail: [email protected]. Introduction Taxonomy, in its widest sense, is at the root of every scientific discipline, which must first define the objects it studies. Then, the attributes of these objects can be used for various classificatory and/or interpretive schemes; for example, the table of elements in chemistry or evolutionary trees in biology. Fisheries science is no different; here the object of study is a fishery, the interaction between species and certain gears, deployed at certain times in certain places. -
Predation and Prey Selectivity by Argyrosomus H%/Epidotus (Osteichthyes: Sciaenidae) in South-Eastem Cape Waters of South Mrica
Predation and prey selectivity by Argyrosomus h%/epidotus (Osteichthyes: Sciaenidae) in south-eastem Cape waters of South Mrica M.J. Smale and M.N. Bruton Port Elizabeth Museum, Port Elizabeth, and .I.L.B. Smith Institute of Ichthyology, Grahamstown Argyrosomus hololepidotus (kob) is a top predator in the Argyrosomus hololepidotus (Lacepede 1802) is a marine and shallow marine environment of the south-eastem Cape. There estuarine sciaenid fish which is found south of the equator is considerable change in prey taken over the size range of from the west African coast to Natal, Madagascar, western predators examined (256 - 1701 mm). Young A. hololepidotus Indian Ocean off Kathiawar (Seshappa) and off the Australian are planktivorous taking swarming mysids, but as they grow they become piscivorous, feeding on both pelagic and coast, at least from Brisbane southwards to the Bass Straight demersal prey associated with soft sediments. The pelagic (Trewavas 1977). cephalopod Lo/igo reynaudi is also taken by large In the south-eastern Cape A. hololepidotus is caught specimens. Prey selection varies with locality and time of throughout the year by the line-fishery, with highest catches year. A field experiment in which the prey were compared recorded between September and February (Smale 1985). with fish caught in a small-mesh net revealed a preference It is common in this area and is the principal species caught for some slow-moving demersal species. The length distri butions of dominant prey species are given and these clear by ski-boats over sandy areas. A. hololepidotus is frequently ly show that larger prey are preferred by larger predators. -
Otolith Atlas for the Western Mediterranean, North and Central Eastern Atlantic
SCIENTIA MARINA 72S1 July 2008, 7-198, Barcelona (Spain) ISSN: 0214-8358 Otolith atlas for the western Mediterranean, north and central eastern Atlantic VICTOR M. TUSET 1, ANTONI LOMBARTE 2 and CARLOS A. ASSIS 3 1 Instituto Canario de Ciencias Marinas, Departamento de Biología Pesquera, P.O. Box. 56, E-35200 Telde (Las Palmas), Canary Islands, Spain. E-mail: [email protected] 2 Institut de Ciències del Mar-CSIC, Departament de Recursos Marins Renovables, Passeig Marítim 37-49, Barcelona 08003, Catalonia, Spain. 3 Instituto de Oceanografia e Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande 1749-016, Lisboa, Portugal. SUMMARY: The sagittal otolith of 348 species, belonging to 99 families and 22 orders of marine Teleostean fishes from the north and central eastern Atlantic and western Mediterranean were described using morphological and morphometric characters. The morphological descriptions were based on the otolith shape, outline and sulcus acusticus features. The mor- phometric parameters determined were otolith length (OL, mm), height (OH, mm), perimeter (P; mm) and area (A; mm2) and were expressed in terms of shape indices as circularity (P2/A), rectangularity (A/(OL×OH)), aspect ratio (OH/OL; %) and OL/fish size. The present Atlas provides information that complements the characterization of some ichthyologic taxa. In addition, it constitutes an important instrument for species identification using sagittal otoliths collected in fossiliferous layers, in archaeological sites or in feeding remains of bony fish predators. Keywords: otolith, sagitta, morphology, morphometry, western Mediterranean, north eastern Atlantic, central eastern Atlantic. RESUMEN: Otolitos de peces del mediterráneo occidental y del atlántico central y nororiental. -
FAMILY Callorhinchidae - Plownose Chimaeras Notes: Callorhynchidae Garman, 1901:77 [Ref
FAMILY Callorhinchidae - plownose chimaeras Notes: Callorhynchidae Garman, 1901:77 [ref. 1541] (family) Callorhinchus [as Callorhynchus, name must be corrected Article 32.5.3; corrected to Callorhinchidae by Goodrich 1909:176 [ref. 32502], confirmed by Nelson 2006:45 [ref. 32486]] GENUS Callorhinchus Lacepède, 1798 - elephantfishes [=Callorhinchus Lacepède [B. G. E.] (ex Gronow), 1798:400, Callorhyncus Fleming [J.], 1822:380, Callorynchus Cuvier [G.] (ex Gronow), 1816:140] Notes: [ref. 2708]. Masc. Chimaera callorynchus Linnaeus, 1758. Type by monotypy. Subsequently described from excellent description by Gronow as Callorhynchus (Cuvier 1829:382) and Callorhincus (Duméril 1806:104); unjustifiably emended (from Gronow 1754) by Agassiz 1846:60 [ref. 64] to Callirhynchus. •Valid as Callorhinchus Lacepède, 1798 -- (Nakamura et al. 1986:58 [ref. 14235], Compagno 1986:147 [5648], Paxton et al. 1989:98 [ref. 12442], Gomon et al. 1994:190 [ref. 22532] as Callorhynchus, Didier 1995:14 [ref. 22713], Paxton et al. 2006:50 [ref. 28994], Gomon 2008:147 [ref. 30616], Di Dario et al. 2011:546 [ref. 31478]). Current status: Valid as Callorhinchus Lacepède, 1798. Callorhinchidae. (Callorhyncus) [ref. 5063]. Masc. Callorhyncus antarcticus Fleming (not of Lay & Bennett 1839), 1822. Type by monotypy. Perhaps best considered an unjustified emendation of Callorhincus Lacepède; virtually no distinguishing features presented, and none for species independent of that for genus. •Synonym of Callorhinchus Lacepède, 1798. Current status: Synonym of Callorhinchus Lacepède, 1798. Callorhinchidae. (Callorynchus) [ref. 993]. Masc. Chimaera callorhynchus Linnaeus, 1758. Type by monotypy. The one included species given as "La Chimère antarctique (Chimaera callorynchus L)." •Synonym of Callorhinchus Lacepède, 1798; both being based on Gronow 1754 (pre-Linnaean). Current status: Synonym of Callorhinchus Lacepède, 1798. -
Copyrighted Material
06_250317 part1-3.qxd 12/13/05 7:32 PM Page 15 Phylum Chordata Chordates are placed in the superphylum Deuterostomia. The possible rela- tionships of the chordates and deuterostomes to other metazoans are dis- cussed in Halanych (2004). He restricts the taxon of deuterostomes to the chordates and their proposed immediate sister group, a taxon comprising the hemichordates, echinoderms, and the wormlike Xenoturbella. The phylum Chordata has been used by most recent workers to encompass members of the subphyla Urochordata (tunicates or sea-squirts), Cephalochordata (lancelets), and Craniata (fishes, amphibians, reptiles, birds, and mammals). The Cephalochordata and Craniata form a mono- phyletic group (e.g., Cameron et al., 2000; Halanych, 2004). Much disagree- ment exists concerning the interrelationships and classification of the Chordata, and the inclusion of the urochordates as sister to the cephalochor- dates and craniates is not as broadly held as the sister-group relationship of cephalochordates and craniates (Halanych, 2004). Many excitingCOPYRIGHTED fossil finds in recent years MATERIAL reveal what the first fishes may have looked like, and these finds push the fossil record of fishes back into the early Cambrian, far further back than previously known. There is still much difference of opinion on the phylogenetic position of these new Cambrian species, and many new discoveries and changes in early fish systematics may be expected over the next decade. As noted by Halanych (2004), D.-G. (D.) Shu and collaborators have discovered fossil ascidians (e.g., Cheungkongella), cephalochordate-like yunnanozoans (Haikouella and Yunnanozoon), and jaw- less craniates (Myllokunmingia, and its junior synonym Haikouichthys) over the 15 06_250317 part1-3.qxd 12/13/05 7:32 PM Page 16 16 Fishes of the World last few years that push the origins of these three major taxa at least into the Lower Cambrian (approximately 530–540 million years ago).