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CHECKLIST and BIOGEOGRAPHY of FISHES from GUADALUPE ISLAND, WESTERN MEXICO Héctor Reyes-Bonilla, Arturo Ayala-Bocos, Luis E
ReyeS-BONIllA eT Al: CheCklIST AND BIOgeOgRAphy Of fISheS fROm gUADAlUpe ISlAND CalCOfI Rep., Vol. 51, 2010 CHECKLIST AND BIOGEOGRAPHY OF FISHES FROM GUADALUPE ISLAND, WESTERN MEXICO Héctor REyES-BONILLA, Arturo AyALA-BOCOS, LUIS E. Calderon-AGUILERA SAúL GONzáLEz-Romero, ISRAEL SáNCHEz-ALCántara Centro de Investigación Científica y de Educación Superior de Ensenada AND MARIANA Walther MENDOzA Carretera Tijuana - Ensenada # 3918, zona Playitas, C.P. 22860 Universidad Autónoma de Baja California Sur Ensenada, B.C., México Departamento de Biología Marina Tel: +52 646 1750500, ext. 25257; Fax: +52 646 Apartado postal 19-B, CP 23080 [email protected] La Paz, B.C.S., México. Tel: (612) 123-8800, ext. 4160; Fax: (612) 123-8819 NADIA C. Olivares-BAñUELOS [email protected] Reserva de la Biosfera Isla Guadalupe Comisión Nacional de áreas Naturales Protegidas yULIANA R. BEDOLLA-GUzMáN AND Avenida del Puerto 375, local 30 Arturo RAMíREz-VALDEz Fraccionamiento Playas de Ensenada, C.P. 22880 Universidad Autónoma de Baja California Ensenada, B.C., México Facultad de Ciencias Marinas, Instituto de Investigaciones Oceanológicas Universidad Autónoma de Baja California, Carr. Tijuana-Ensenada km. 107, Apartado postal 453, C.P. 22890 Ensenada, B.C., México ABSTRACT recognized the biological and ecological significance of Guadalupe Island, off Baja California, México, is Guadalupe Island, and declared it a Biosphere Reserve an important fishing area which also harbors high (SEMARNAT 2005). marine biodiversity. Based on field data, literature Guadalupe Island is isolated, far away from the main- reviews, and scientific collection records, we pres- land and has limited logistic facilities to conduct scien- ent a comprehensive checklist of the local fish fauna, tific studies. -
Diaphus Taaningi Norman, the Principal Component If a Shallow Sound-Scattering Layer in the Cariaco Trench, Venezuela'
The Journal of Marine Research is an online peer-reviewed journal that publishes original research on a broad array of topics in physical, biological, and chemical oceanography. In publication since 1937, it is one of the oldest journals in American marine science and occupies a unique niche within the ocean sciences, with a rich tradition and distinguished history as part of the Sears Foundation for Marine Research at Yale University. Past and current issues are available at journalofmarineresearch.org. Yale University provides access to these materials for educational and research purposes only. Copyright or other proprietary rights to content contained in this document may be held by individuals or entities other than, or in addition to, Yale University. You are solely responsible for determining the ownership of the copyright, and for obtaining permission for your intended use. Yale University makes no warranty that your distribution, reproduction, or other use of these materials will not infringe the rights of third parties. This work is licensed under the Creative Commons Attribution- NonCommercial-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ or send a letter to Creative Commons, PO Box 1866, Mountain View, CA 94042, USA. Journal of Marine Research, Sears Foundation for Marine Research, Yale University PO Box 208118, New Haven, CT 06520-8118 USA (203) 432-3154 fax (203) 432-5872 [email protected] www.journalofmarineresearch.org Diaphus taaningi Norman, the Principal Component if a Shallow Sound-Scattering Layer in the Cariaco Trench, Venezuela' Ronald C. Baird University of South Florida Department of Marine Science St. -
Myctophidae, Teleostei)
BULLETIN DE [.'INSTITUT ROYAL DES SCIENCES NATURELLES DE BELGIQUE SCIENCES DE LA TERRE, 70: 185-206, 2000 BULLETIN VAN HET KONINKLIJK BELGISCH INSTITUUT VOOR NATUURWETENSCHAPPEN AARDWETENSCHAPPEN, 70: 185-206, 2000 Diaphus Otoliths from the European Neogene (Myctophidae, Teleostei) by Rostislav BRZOBOHATY & Dirk NOLF Abstract and in most species, only adult and large otoliths (larger than 2 mm) show clear diagnostic features, while juve The revision of Neogene otoliths of the myctophid genusDiaphus, niles cannot be distinguished. The other main problem is based on extensive otolith collections in the Aquitaine Basin, in South eastern France, northern Italy. Mediterranean Spain, the Paratethys and that in several Recent D iaphus species, even at the adult the North Sea Basin, has proved the validity of fourteen nominal stage, the otoliths show only a very generalized morphol species, among which two are new: Diaphus hefralai an d D. carallo- ogy (see N o lf & C a p p e t t a , 1989, pi. 9, figs. 12-22). In nis. None of these species has been recorded previously from Oligo fossil associations, such otoliths remain predominantly cène deposits, and only four are still living today. unidentified; in many cases, it is impossible to state if Key-words: D iaphus, Myctophidae, otoliths, Neogene. such forms represent species with a more generalized morphology, or if they are juveniles of species that aquire diagnostic features only at larger sizes (see B r z o b o h a t y Résumé & N o l f . 1995, p. 257 for a more extensive discussion). Practically, this means that in most fossil associations, La révision des espèces oligocènes du genre D iaphus, basée sur un only about 5 to 10 % of the D iaphus otoliths can be abondant matériel d'otolithes récoltées dans le Bassin d'Aquitaine, le confidently identified at the species level. -
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. -
Review: the Energetic Value of Zooplankton and Nekton Species of the Southern Ocean
Marine Biology (2018) 165:129 https://doi.org/10.1007/s00227-018-3386-z REVIEW, CONCEPT, AND SYNTHESIS Review: the energetic value of zooplankton and nekton species of the Southern Ocean Fokje L. Schaafsma1 · Yves Cherel2 · Hauke Flores3 · Jan Andries van Franeker1 · Mary‑Anne Lea4 · Ben Raymond5,4,6 · Anton P. van de Putte7 Received: 8 March 2018 / Accepted: 5 July 2018 / Published online: 18 July 2018 © The Author(s) 2018 Abstract Understanding the energy fux through food webs is important for estimating the capacity of marine ecosystems to support stocks of living resources. The energy density of species involved in trophic energy transfer has been measured in a large number of small studies, scattered over a 40-year publication record. Here, we reviewed energy density records of Southern Ocean zooplankton, nekton and several benthic taxa, including previously unpublished data. Comparing measured taxa, energy densities were highest in myctophid fshes (ranging from 17.1 to 39.3 kJ g−1 DW), intermediate in crustaceans (7.1 to 25.3 kJ g−1 DW), squid (16.2 to 24.0 kJ g−1 DW) and other fsh families (14.8 to 29.9 kJ g−1 DW), and lowest in jelly fsh (10.8 to 18.0 kJ g−1 DW), polychaetes (9.2 to 14.2 kJ g−1 DW) and chaetognaths (5.0–11.7 kJ g−1 DW). Data reveals diferences in energy density within and between species related to size, age and other life cycle parameters. Important taxa in Antarctic food webs, such as copepods, squid and small euphausiids, remain under-sampled. -
Age and Growth of Brauer's Lanternfish Gymnoscopelus Braueri and Rhombic Lanternfish Krefftichthys Anderssoni (Family Myctophidae) in the Scotia Sea, Southern Ocean
Received: 22 July 2019 Accepted: 14 November 2019 DOI: 10.1111/jfb.14206 REGULAR PAPER FISH Age and growth of Brauer's lanternfish Gymnoscopelus braueri and rhombic lanternfish Krefftichthys anderssoni (Family Myctophidae) in the Scotia Sea, Southern Ocean Ryan A. Saunders1 | Silvia Lourenço2,3 | Rui P. Vieira4 | Martin A. Collins1 | Carlos A. Assis5,6 | Jose C. Xavier7,1 1British Antarctic Survey, Natural Environment Research Council, Cambridge, UK Abstract 2MARE - Marine and Environmental Sciences This study examines age and growth of Brauer's lanternfish Gymnoscopelus braueri and Centre, Polytechnic of Leiria, Peniche, Portugal rhombic lanternfish Krefftichthys anderssoni from the Scotia Sea in the Southern Ocean, 3CIIMAR/CIMAR, Interdisciplinary Centre of Marine and Environmental Research, through the analysis of annual growth increments deposited on sagittal otoliths. Oto- University of Porto, Matosinhos, Portugal lith pairs from 177 G. braueri and 118 K. anderssoni were collected in different seasons 4 Centre for Environment Fisheries and from the region between 2004 and 2009. Otolith-edge analysis suggested a seasonal Aquaculture Sciences, Lowestoft, UK change in opaque and hyaline depositions, indicative of an annual growth pattern, 5MARE-ULisboa – Marine and Environmental Sciences Centre, Faculty of Sciences, although variation within the populations of both species was apparent. Age estimates University of Lisbon, Lisbon, Portugal varied from 1 to 6 years for G. braueri (40 to 139 mm standard length; LS)andfrom 6Department of Animal Biology, Faculty of Sciences, University of Lisbon, Lisbon, Portugal 0 to 2 years for K. anderssoni (26 to 70 mm LS). Length-at-age data were broadly con- 7Department of Life Sciences, MARE-UC, sistent with population cohort parameters identified in concurrent length-frequency University of Coimbra, Coimbra, Portugal data from the region for both species. -
Order MYCTOPHIFORMES NEOSCOPELIDAE Horizontal Rows
click for previous page 942 Bony Fishes Order MYCTOPHIFORMES NEOSCOPELIDAE Neoscopelids By K.E. Hartel, Harvard University, Massachusetts, USA and J.E. Craddock, Woods Hole Oceanographic Institution, Massachusetts, USA iagnostic characters: Small fishes, usually 15 to 30 cm as adults. Body elongate with no photophores D(Scopelengys) or with 3 rows of large photophores when viewed from below (Neoscopelus).Eyes variable, small to large. Mouth large, extending to or beyond vertical from posterior margin of eye; tongue with photophores around margin in Neoscopelus. Gill rakers 9 to 16. Dorsal fin single, its origin above or slightly in front of pelvic fin, well in front of anal fins; 11 to 13 soft rays. Dorsal adipose fin over end of anal fin. Anal-fin origin well behind dorsal-fin base, anal fin with 10 to 14 soft rays. Pectoral fins long, reaching to about anus, anal fin with 15 to 19 rays.Pelvic fins large, usually reaching to anus.Scales large, cycloid, and de- ciduous. Colour: reddish silvery in Neoscopelus; blackish in Scopelengys. dorsal adipose fin anal-fin origin well behind dorsal-fin base Habitat, biology, and fisheries: Large adults of Neoscopelus usually benthopelagic below 1 000 m, but subadults mostly in midwater between 500 and 1 000 m in tropical and subtropical areas. Scopelengys meso- to bathypelagic. No known fisheries. Remarks: Three genera and 5 species with Solivomer not known from the Atlantic. All Atlantic species probably circumglobal . Similar families in occurring in area Myctophidae: photophores arranged in groups not in straight horizontal rows (except Taaningichthys paurolychnus which lacks photophores). Anal-fin origin under posterior dorsal-fin anal-fin base. -
Frozen Desert Alive the Role of Sea Ice for Pelagic Macrofauna and Its Predators: Implications for the Antarctic Pack-Ice Food Web
Frozen Desert Alive The role of sea ice for pelagic macrofauna and its predators: implications for the Antarctic pack-ice food web Hauke Flores FrozenDesertAlive �-*#-$1#'!#$-0.#*%'!+!0-$3,,"'21.0#"2-01S '+.*'!2'-,1$-02&#,20!2'!.!)V'!#$--"5# 0',2#" 7-,1#,--'#, T4TQ""# "*#!20-,'!4#01'-,4'* *#2S &22.S 555T03%T,* ' *'-2&##) !2*-%' #12,"#, #*#).3 03% "'11#022'#1 ',"#6 %&'(S[YZV[RVXVXVVUU[VT 1%23&4(%5"1&%"%617(%(6"( FrozenDesertAlive �-*#-$1#'!#$-0.#*%'!+!0-$3,,"'21.0#"2-01S '+.*'!2'-,1$-02&#,20!2'!.!)V'!#$--"5# 17"8&9:1%8 2#04#0)0'(%',%4,"-!2-02',"# <'1)3,"##,(23305#2#,1!&..#, ,"#1'()13,'4#01'2#'260-,',%#, -.%#8%4,"# 1#!2-0>%,'$'!31Q"0T8T?5021Q ',-.#, 02#4#0"#"'%#,-. 40'("%S+#'TRR[ -+SUTSW330 "--0 HaukeFlores %# -0#,-.SZ1#.2#+ #0S[YV 2#'0#+#0&4#, 0-+-2-0 S0-$T"0T<T2T<-*$$ 9-.0-+-2-0 SB0T2TT4,80,#)#0 '#--0"#*',%1!-++'11'# S0-$T"0T'0T:T2T<T"#'0 S0-$T"0T4T5T'2&+,, S0-$T"0T8TT>T5-*!)#02 %,+#+-07-$+7%0,"+-2� %,6#"#,)#,,+#',#60-!+322#0 6'1#*8*-0#1 TV&#.TS[TSVTX2,TTRRZ Contents ",%*'1&13++07 Z B32!&13++07 SS 6#0+,13++07 SV 9&.2#0S 6#,#0*%,20-"3!2'-, S[ 9&.2#0T B'#2-$25-'!#$'1&1.#!'#1$0-+2&#&-32&&*," U[ %1*,"1,""*#.&,2%1*,"1QChampsocephalusgunnari ,"Chaenocephalusaceratus',TRRSTRRU PolarBiology27(2004)119R129 9&.2#0U ",#0%7!-,2#,2-$,20!2'!+#1-.#*%'!$'1S XS '+.*'!2'-,1$-02&#+0',#$--"5# PolarBiology29(2006)10451051 9&.2#0V B'120' 32'-,Q 3,",!#,"#!-*-%'!*0#*#4,!#-$ YU .#*%'!$'1',2P#4&#Q&-32�,7!#, MarineEcologyProgressSeries367(2008)271282 9&.2#0W -
Using Molecular Identification of Ichthyoplankton to Monitor
Molecular Identification of Ichthyoplankton in Cabo Pulmo National Park 1 Using molecular identification of ichthyoplankton to monitor 2 spawning activity in a subtropical no-take Marine Reserve 3 4 5 6 Ana Luisa M. Ahern1, *, Ronald S. Burton1, Ricardo J. Saldierna-Martínez2, Andrew F. Johnson1, 7 Alice E. Harada1, Brad Erisman1,4, Octavio Aburto-Oropeza1, David I. Castro Arvizú3, Arturo R. 8 Sánchez-Uvera2, Jaime Gómez-Gutiérrez2 9 10 11 12 1Marine Biology Research Division, Scripps Institution of Oceanography, University of California 13 San Diego, La Jolla, California, USA 14 2Departamento de Plancton y Ecología Marina, Centro Interdisciplinario de Ciencias Marinas, 15 Instituto Politécnico Nacional, CP 23096, La Paz, Baja California Sur, Mexico 16 3Cabo Pulmo National Park, Baja California Sur, Mexico 17 4The University of Texas at Austin, Marine Science Institute, College of Natural Sciences, 18 Port Aransas, Texas, USA 19 20 21 22 23 24 25 *Corresponding author: [email protected] 1 Molecular Identification of Ichthyoplankton in Cabo Pulmo National Park 26 ABSTRACT: Ichthyoplankton studies can provide valuable information on the species richness 27 and spawning activity of fishes, complementing estimations done using trawls and diver surveys. 28 Zooplankton samples were collected weekly between January and December 2014 in Cabo 29 Pulmo National Park, Gulf of California, Mexico (n=48). Fish larvae and particularly eggs are 30 difficult to identify morphologically, therefore the DNA barcoding method was employed to 31 identify 4,388 specimens, resulting in 157 Operational Taxonomic Units (OTUs) corresponding 32 to species. Scarus sp., Halichoeres dispilus, Xyrichtys mundiceps, Euthynnus lineatus, 33 Ammodytoides gilli, Synodus lacertinus, Etrumeus acuminatus, Chanos chanos, Haemulon 34 flaviguttatum, and Vinciguerria lucetia were the most abundant and frequent species recorded. -
A Review of Lanternfishes (Families: Myctophidae and Neoscopelidae)
Zoological Studies 40(2): 103-126 (2001) A Review of Lanternfishes (Families: Myctophidae and Neoscopelidae) and Their Distributions around Taiwan and the Tungsha Islands with Notes on Seventeen New Records John Ta-Ming Wang* and Che-Tsung Chen Graduate School of Fisheries Science, National Taiwan Ocean University, Keelung, Taiwan 202, R.O.C. Fax: 886-2-28106688. E-mail: [email protected] (Accepted December 20, 2000) John Ta-Ming Wang and Che-Tsung Chen (2001) A review of lanternfishes (Families: Myctophidae and Neoscopelidae) and their distributions around Taiwan and the Tungsha Islands with notes on seventeen new records. Zoological Studies 40(2): 103-126. Lanternfishes collected during 9 cruises from 1991 to 1997 were studied. The area sampled lies between 19°N and 25°N and 114°E and 123°E. The specimens collected in this area comprise 40 species belong to 16 genera, among which 17 species are first records. These first record species include Benthosema fibulatum, Bolinichthys supralateralis, Electrona risso, Hygophum proximum, H. reinhardtii, Lampadena anomala, Lobianchia gemellarii, Lampanyctus niger, L. turneri, L. tenuiformis, Myctophum asperum, M. aurolaternatum, M. nitidulum, M. spinosum, Notolychnus valdiviae, Notoscopelus caudispinosus, and N. resplendens. Among these, six species, Bolinichthys supralateralis, Electrona risso, Lampanyctus turneri, Lampadena anomala, Notolychnus valdiviae, and Notoscopelus caudispinosus, are first records for the South China Sea, and the species, Lampadena anomala is a new record for Asian oceans (Table 1). Four species (Triphoturus microchir, Diaphus diadematus, D. latus, and D. taaningi) were controversial in previous reports, so they are discussed in this study. Geographic distributions and localities of catches of all lanternfish species are shown on the maps (Figs. -
Inventory and Atlas of Corals and Coral Reefs, with Emphasis on Deep-Water Coral Reefs from the U
Inventory and Atlas of Corals and Coral Reefs, with Emphasis on Deep-Water Coral Reefs from the U. S. Caribbean EEZ Jorge R. García Sais SEDAR26-RD-02 FINAL REPORT Inventory and Atlas of Corals and Coral Reefs, with Emphasis on Deep-Water Coral Reefs from the U. S. Caribbean EEZ Submitted to the: Caribbean Fishery Management Council San Juan, Puerto Rico By: Dr. Jorge R. García Sais dba Reef Surveys P. O. Box 3015;Lajas, P. R. 00667 [email protected] December, 2005 i Table of Contents Page I. Executive Summary 1 II. Introduction 4 III. Study Objectives 7 IV. Methods 8 A. Recuperation of Historical Data 8 B. Atlas map of deep reefs of PR and the USVI 11 C. Field Study at Isla Desecheo, PR 12 1. Sessile-Benthic Communities 12 2. Fishes and Motile Megabenthic Invertebrates 13 3. Statistical Analyses 15 V. Results and Discussion 15 A. Literature Review 15 1. Historical Overview 15 2. Recent Investigations 22 B. Geographical Distribution and Physical Characteristics 36 of Deep Reef Systems of Puerto Rico and the U. S. Virgin Islands C. Taxonomic Characterization of Sessile-Benthic 49 Communities Associated With Deep Sea Habitats of Puerto Rico and the U. S. Virgin Islands 1. Benthic Algae 49 2. Sponges (Phylum Porifera) 53 3. Corals (Phylum Cnidaria: Scleractinia 57 and Antipatharia) 4. Gorgonians (Sub-Class Octocorallia 65 D. Taxonomic Characterization of Sessile-Benthic Communities 68 Associated with Deep Sea Habitats of Puerto Rico and the U. S. Virgin Islands 1. Echinoderms 68 2. Decapod Crustaceans 72 3. Mollusks 78 E. -
Ketibunder Ecological2008.Pdf
Disclaimer note This information should be considered accurate as of the date prepared, namely 2007. You acknowledge that this information may change over time and you should not assume that this information is accurate at a later date. WWF-Pakistan and the Royal Netherlands Embassy accept no responsibility for any errors, deviations and omissions in information compiled by independent consultants in this report. Please send comments regarding any errors, inconsistencies, unacknowledged use of source material or any other issue regarding this ecological baseline report as it will help to curate this database. Comments can be submitted to [email protected] Detailed Ecological Assessment Report 2008 – Keti Bunder Table of contents i List of tables vi List of figures viii List of maps and images x List of Acronyms xi List of resource people/consultants xiii Acknowledgement xiv Executive summary xv Chapter 1 Introduction…………………..………………………………… 1 1.1 Introduction to Keti Bunder….……………………………… 2 1.1.1 State of natural resources…………………………………….. 4 1.1.2 Livelihood and social aspects…………………………………. 5 1.2 Rationale and Objectives…………………………………… 6 1.2.1 Large Mammals Survey……………………………………….. 6 1.2.1.1 Rationale………………………………………………………… 6 1.2.1.2 Objectives of the study………………………………………… 7 1.2.2 Small mammal survey…………………………………………. 7 1.2.2.1 Rationale………………………………………………………… 7 1.2.2.2 Objectives of the study………………………………………... 9 1.2.3 Reptiles and amphibians survey……………………………… 10 1.2.3.1 Rationale………………………………………………………… 10 1.2.3.2 Objectives of the study………………………………………... 10 1.2.4 Birds survey…………………………………………………….. 11 1.2.4.1 Rationale………………………………………………………… 11 1.2.4.2 Objectives of the study………………………………………… 11 1.2.5 Marine Fisheries…………………………………………..