Grazing on the Epiphytic Community of Posidonia Oceanica (L.)Delile: an Assessment of Its Relevance As a Buffering Process of Eutrophication Effects
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Bioone? RESEARCH
RESEARCH BioOne? EVOLVED Proximate Nutrient Analyses of Four Species of Submerged Aquatic Vegetation Consumed by Florida Manatee (Trichechus manatus latirostris) Compared to Romaine Lettuce (Lactuca sativa var. longifolia) Author(s): Jessica L. Siegal-Willott, D.V.M., Dipl. A.C.Z.M., Kendal Harr, D.V.M., M.S., Dipl. A.C.V.P., Lee-Ann C. Hayek, Ph.D., Karen C. Scott, Ph.D., Trevor Gerlach, B.S., Paul Sirois, M.S., Mike Renter, B.S., David W. Crewz, M.S., and Richard C. Hill, M.A., Vet.M.B., Ph.D., M.R.C.V.S. Source: Journal of Zoo and Wildlife Medicine, 41(4):594-602. 2010. Published By: American Association of Zoo Veterinarians DOI: 10.1638/2009-0118.1 URL: http://www.bioone.org/doi/full/10.1638/2009-0118.1 BioOne (www.bioone.org) is an electronic aggregator of bioscience research content, and the online home to over 160 journals and books published by not-for-profit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne's Terms of Use, available at www.bioone.org/page/terms of use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. -
<I>Syringodium Filiforme</I>
BULLETIN OF MARINE SCIENCE, 83(3): 571–585, 2008 LEAF GROWTH OF THE SEAGRASS SYRINGODIUM FILIFORME IN OUTER FLORIDA BAY, FLORIDA Arthur C. Schwarzschild, W. Judson Kenworthy, and Joseph C. Zieman ABSTRACT Leaf growth of the seagrass Syringodium filiforme (Kütz., 1860) was determined using a new technique based on the growth of emergent leaves (EL method) and compared to the more labor intensive repeated measurements (RM) and demo- graphic allometric age reconstruction techniques (DA). All three techniques were used to compare leaf growth dynamics of plants with different morphologies at two sites, a shallow water (0.5 m) banktop and an adjacent deeper water (1.5 m) environ- ment in outer Florida Bay, Florida. Leaf formation rates (Leaf Plastochrone Interval or PI) determined using the EL and RM methods were nearly identical, with means of 20 and 21 d leaf–1 at both sites, significantly faster than the 30 d leaf–1 calculated using the DA method. The EL method produced the highest estimate of leaf growth, 1.8 and 1.9 cm d–1 at the 0.5 m and 1.5 m sites, respectively, followed by the RM method (1.3 and 1.3 cm d–1) and the DA method (1.0 and 1.1 cm d–1). None of the methods detected differences in leaf PI, leaf growth or leaf fragmentation rates be- tween sites. However, leaves at the 1.5 m site typically retained intact leaf tips longer than those at the 0.5 m site, and total leaf lifespan was longer at the 1.5 m site. -
Amphipods Are Not All Created Equal
354 1 Lewis, S. M., and B. Kensley. 1982. Notes on the ecology Steinberg, P. D. 1986. Chemical defenses and the suscep and behaviour of Pseudoamphithoides incurvaria (Just) tibility of tropical marine brown algae to herbivores. Oeco (Crustacea, Amphipoda, Ampithoidae). Journal of Natural logia (Berlin) 69:628-630. History 16:267-274. Stoner, A. W. 1980. Perception and choice of substratum Martin, A. L. 1966. Feeding and digestion in two intertidal by epifaunal amphipods associated with seagrass. Marine gammarids: Marinogammarus obtusatus and M. pirloti. Ecology Progress Series 3: 105-111. Journal of Zoology 148:515-552. Virnstein, R. W., and M. C. Curran. 1986. Colonization of Nelson, W. G. 1979. An analysis of structural pattern in an artificial seagrass versus time and distance from source. eelgrass (Zostera marina L.) amphipod community. Jour Marine Ecology Progress Series 29:279-288. nal of Experimental Marine Biology and Ecology 39:231- Virnstein, R. W., and R. K. Howard. 1987. Motile epifauna 264. of marine macrophytes in the Indian River Lagoon, Fl. II. --. 1980. A comparative study of amphipods in sea Comparisons between drift algae and three species of sea grass from Florida to Nova Scotia. Bulletin of Marine Sci grasses. Bulletin of Marine Science 41: 13-26. ence 30:80-89. Zimmerman, R., R. Gibson, and J. Harrington. 1979. Her Nicotri, M. E. 1977. The impact of crustacean herbivores bivory and detritivory among gammaridean amphipods on cultured seaweed populations. Aquaculture 12: 127-136. from a Florida seagrass community. Marine Biology 54: Orth, R. J., and J. van Montfrans. 1984. Epiphyte-seagrass 41-47. -
Global Seagrass Distribution and Diversity: a Bioregional Model ⁎ F
Journal of Experimental Marine Biology and Ecology 350 (2007) 3–20 www.elsevier.com/locate/jembe Global seagrass distribution and diversity: A bioregional model ⁎ F. Short a, , T. Carruthers b, W. Dennison b, M. Waycott c a Department of Natural Resources, University of New Hampshire, Jackson Estuarine Laboratory, Durham, NH 03824, USA b Integration and Application Network, University of Maryland Center for Environmental Science, Cambridge, MD 21613, USA c School of Marine and Tropical Biology, James Cook University, Townsville, 4811 Queensland, Australia Received 1 February 2007; received in revised form 31 May 2007; accepted 4 June 2007 Abstract Seagrasses, marine flowering plants, are widely distributed along temperate and tropical coastlines of the world. Seagrasses have key ecological roles in coastal ecosystems and can form extensive meadows supporting high biodiversity. The global species diversity of seagrasses is low (b60 species), but species can have ranges that extend for thousands of kilometers of coastline. Seagrass bioregions are defined here, based on species assemblages, species distributional ranges, and tropical and temperate influences. Six global bioregions are presented: four temperate and two tropical. The temperate bioregions include the Temperate North Atlantic, the Temperate North Pacific, the Mediterranean, and the Temperate Southern Oceans. The Temperate North Atlantic has low seagrass diversity, the major species being Zostera marina, typically occurring in estuaries and lagoons. The Temperate North Pacific has high seagrass diversity with Zostera spp. in estuaries and lagoons as well as Phyllospadix spp. in the surf zone. The Mediterranean region has clear water with vast meadows of moderate diversity of both temperate and tropical seagrasses, dominated by deep-growing Posidonia oceanica. -
Morpho-Chronological Variations and Primary Production in Posidonia
Morpho-chronological variations and primary production in Posidonia sea grass from Western Australia Gérard Pergent, Christine Pergent-Martini, Catherine Fernandez, Pasqualini Vanina, Diana Walker To cite this version: Gérard Pergent, Christine Pergent-Martini, Catherine Fernandez, Pasqualini Vanina, Diana Walker. Morpho-chronological variations and primary production in Posidonia sea grass from Western Aus- tralia. Journal of the Marine Biological Association of the United Kingdom, Cambridge University Press, 2004, 84 (5), pp.895-899. 10.1017/S0025315404010161h. hal-01768985 HAL Id: hal-01768985 https://hal.archives-ouvertes.fr/hal-01768985 Submitted on 17 Apr 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. J. Mar. Biol. Ass. U.K. (2004), 84, 895^899 Printed in the United Kingdom Morpho-chronological variations and primary production in Posidonia sea grass from Western Australia P Ge¤rard Pergent* , Christine Pergent-Martini*, Catherine Fernandez*, O Vanina Pasqualini* and Diana Walker O *Equipe Ecosyste' mes Littoraux, Faculty of Sciences, -
The Global Distribution and Status of Seagrass Ecosystems
The global distribution and status of seagrass ecosystems ^^ ^^^H Discussion paper prepared for tlie UNEP-WCWIC Global Seagrass Workshop St Pete's Beach, Florida, 9 November, 2001 Prepared by: Mark D. Spalding, Michelle L. Taylor, Sergio Martins, Edmund P. Green, and Mary Edwards WA.. WORLD CONSERVATION MONITORING CENTRE Digitized by tine Internet Archive in 2010 witii funding from UNEP-WCIVIC, Cambridge Iittp://www.archive.org/details/globaldistributi01spal The global distribution and status of seagrass ecosystems Discussion paper prepared for tlie UNEP-WCIVIC Global Seagrass Workshop St Pete's Beach, Florida, 9 November, 2001 Prepared by: Mark D. Spalding, Michelle L. Taylor, Sergio Martins, Edmund P. Green, and Mary Edwards With assistance from: Mark Taylor and Corinna Ravilious Table of Contents Introduction to the workshop 2 The global distribution and status of seagrass ecosystems 3 Introduction 3 Definitions 3 The diversity of seagrasses 3 Species distribution 4 Associated Species 6 Productivity and biomass 7 The distribution and area of seagrass habitat 8 The value of seagrasses 13 Threats to seagrasses 13 Management Interventions 14 Bibliography; 16 29 Annex 1 : Seagrass Species Lists by Country Annex 2 - Species distribution maps 34 Annex 3 - Seagrass distribution maps 68 74 Annex 4 -Full list of MPAs by country ; /4^ ] UNEP WCMC Introduction to the workshop The Global Seagrass Workshop of 9 November 2001 has been set up with the expressed aim to develop a global synthesis on the distribution and status of seagrasses world-wide. Approximately 20 seagrass experts from 14 counu-ies, representing all of the major seagrass regions of the world have been invited to share their knowledge and expertise. -
1 Phylogenetic Regionalization of Marine Plants Reveals Close Evolutionary Affinities Among Disjunct Temperate Assemblages Barna
Phylogenetic regionalization of marine plants reveals close evolutionary affinities among disjunct temperate assemblages Barnabas H. Darua,b,*, Ben G. Holtc, Jean-Philippe Lessardd,e, Kowiyou Yessoufouf and T. Jonathan Daviesg,h aDepartment of Organismic and Evolutionary Biology and Harvard University Herbaria, Harvard University, Cambridge, MA 02138, USA bDepartment of Plant Science, University of Pretoria, Private Bag X20, Hatfield 0028, Pretoria, South Africa cDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot SL5 7PY, United Kingdom dQuebec Centre for Biodiversity Science, Department of Biology, McGill University, Montreal, QC H3A 0G4, Canada eDepartment of Biology, Concordia University, Montreal, QC, H4B 1R6, Canada; fDepartment of Environmental Sciences, University of South Africa, Florida campus, Florida 1710, South Africa gDepartment of Biology, McGill University, Montreal, QC H3A 0G4, Canada hAfrican Centre for DNA Barcoding, University of Johannesburg, PO Box 524, Auckland Park, Johannesburg 2006, South Africa *Corresponding author Email: [email protected] (B.H. Daru) Running head: Phylogenetic regionalization of seagrasses 1 Abstract While our knowledge of species distributions and diversity in the terrestrial biosphere has increased sharply over the last decades, we lack equivalent knowledge of the marine world. Here, we use the phylogenetic tree of seagrasses along with their global distributions and a metric of phylogenetic beta diversity to generate a phylogenetically-based delimitation of marine phytoregions (phyloregions). We then evaluate their evolutionary affinities and explore environmental correlates of phylogenetic turnover between them. We identified 11 phyloregions based on the clustering of phylogenetic beta diversity values. Most phyloregions can be classified as either temperate or tropical, and even geographically disjunct temperate regions can harbor closely related species assemblages. -
Observations of Fin Whales (Balaenoptera Physalus
SHORT COMMUNICATION EIGHT GASTROPODS NEW FOR THE MARINE FAUNA OF MADEIRA PETER WIRTZ WIRTZ, P. 2005. Eight gastropods new for the marine fauna of Madeira. Arquipélago. Life and Marine Sciences 22A: 77-80. The prosobranchs Architectonica nobilis and Smaragdia viridis and the opisthobranchs Arminia maculata, Cyerce cf. graeca, Elysia papillosa, Petalifera petalifera, Pleurobranchaea meckeli and Pleurobranchus testudinarius are recorded from Madeira Island for the first time. Peter Wirtz (email: [email protected]) - Centro de Ciências do Mar, Universidade do Algarve, Campus de Gambelas, PT-8005-139 Faro, Portugal. INTRODUCTION RESULTS During SCUBA dives along the coasts of Madeira A) “Prosobranchia” Island, I again noted the presence of numerous species not yet recorded for the area. Similar to Architectonica nobilis Röding, 1798 previous publications (e.g. WIRTZ 1998, 1999), I This species apparently is common on sandy here report on eight marine gastropods new for bottom near Caniçal (south-eastern coast of the fauna of Madeira. Madeira); one to three living animals were seen there in 15 – 25 m depth during each of six night MATERIAL AND METHODS dives. Middle of July 2005 a copulating pair was encountered. The photo (Fig. 1), taken at night in All records were made while SCUBA diving in a about 15 m depth, shows a living animal. depth range of 1 – 60 m. Animals were Architectonica nobilis is a tropical West photographed in the field, collected, and African species previously known from Angola preserved in alcohol. In some cases, specimens or north to the Canary Islands (POPPE & GOTO 1991; photos were sent to experts for confirmation of ROLÁN 2005). -
Mollusc Fauna of Iskenderun Bay with a Checklist of the Region
www.trjfas.org ISSN 1303-2712 Turkish Journal of Fisheries and Aquatic Sciences 12: 171-184 (2012) DOI: 10.4194/1303-2712-v12_1_20 SHORT PAPER Mollusc Fauna of Iskenderun Bay with a Checklist of the Region Banu Bitlis Bakır1, Bilal Öztürk1*, Alper Doğan1, Mesut Önen1 1 Ege University, Faculty of Fisheries, Department of Hydrobiology Bornova, Izmir. * Corresponding Author: Tel.: +90. 232 3115215; Fax: +90. 232 3883685 Received 27 June 2011 E-mail: [email protected] Accepted 13 December 2011 Abstract This study was performed to determine the molluscs distributed in Iskenderun Bay (Levantine Sea). For this purpose, the material collected from the area between the years 2005 and 2009, within the framework of different projects, was investigated. The investigation of the material taken from various biotopes ranging at depths between 0 and 100 m resulted in identification of 286 mollusc species and 27542 specimens belonging to them. Among the encountered species, Vitreolina cf. perminima (Jeffreys, 1883) is new record for the Turkish molluscan fauna and 18 species are being new records for the Turkish Levantine coast. A checklist of Iskenderun mollusc fauna is given based on the present study and the studies carried out beforehand, and a total of 424 moluscan species are known to be distributed in Iskenderun Bay. Keywords: Levantine Sea, Iskenderun Bay, Turkish coast, Mollusca, Checklist İskenderun Körfezi’nin Mollusca Faunası ve Bölgenin Tür Listesi Özet Bu çalışma İskenderun Körfezi (Levanten Denizi)’nde dağılım gösteren Mollusca türlerini tespit etmek için gerçekleştirilmiştir. Bu amaçla, 2005 ve 2009 yılları arasında sürdürülen değişik proje çalışmaları kapsamında bölgeden elde edilen materyal incelenmiştir. -
Results of the Fifth Eelgrass (Zostera Marina) Mapping Survey: Status and Distribution in Newport Bay, Newport Beach, California 2016 Survey
RESULTS OF THE FIFTH EELGRASS (ZOSTERA MARINA) MAPPING SURVEY: STATUS AND DISTRIBUTION IN NEWPORT BAY, NEWPORT BEACH, CALIFORNIA 2016 SURVEY Prepared for: City of Newport Beach Public Works, Harbor Resources Division 100 Civic Center Drive, Newport Beach, California 92660 Contact: Chris Miller, Harbor Resources Manager [email protected] (949) 644-3043 Prepared by: Coastal Resources Management, Inc. 144 N. Loreta Walk, Long Beach, CA 90803 Contact: Rick Ware, Senior Marine Biologist [email protected] (949) 412-9446 June 15th, 2017 Revised July 10th, 2017 TABLE OF CONTENTS Section Page 1.0 INTRODUCTION ..................................................................................................................... 1 1.1 Project Purpose ........................................................................................................................... 1 1.2 Background ................................................................................................................................. 1 1.3 Project Setting ............................................................................................................................. 2 1.4 Summary of Eelgrass Biology and Its Importance ................................................................... 4 1.5 Eelgrass Regulatory Setting ....................................................................................................... 6 2.0 METHODS AND MATERIALS ............................................................................................. -
Annual Report 2011-12
G.12 Museum of New Zealand Te Papa Tongarewa Te P ūrongo ā Tau Annual Report 2011/12 In accordance with section 150 of the Crown Entities Act 2004, this annual report of the Museum of New Zealand Te Papa Tongarewa for 2011/12 is presented to the House of Representatives. NG Ā IHIRANGI – CONTENTS Part 1: Ng ā Tau āki Tirohanga Wh ānui: Overview Statements From the Chairman 1 From the Chief Executive and Kaihaut ū 3 Performance at a glance 6 Part 2: Museum Of New Zealand Te Papa Tongarewa Accountability and legislation 10 Governance and management 12 Part 3: Te Tau āki o ng ā Paearu Ratonga : Statement of Service Performance Performance Framework 15 Statement of Service Performance 17 Part Four: Te Āheitanga – ā-Tangata, ā-Tukanga, ā-Hangarau: Capability – People, Process, and Technology People, Process, and Technology 38 Workforce profile and equal employment opportunities 42 Te Papa as a good employer 43 Part 5: Te Tau āki o ng ā Paearu P ūtea : Financial Statements Financial Statements 51 Āpitihanga – Appendices Expert Knowledge Exchanges and Workshops 89 Loans 93 Acquisitions 97 Publications and Conference Presentations 107 Ō m ātou hoa – our partners 123 PART 1: NG Ā TAU ĀKI TIROHANGA WH ĀNUI – OVERVIEW CHAIRMAN’S STATEMENT E te hunga kua ngaro atu, tikapa ana koutou ki te rangi te rau o te Amokura hei whangaia atu i t āku nei titiro. He ao uru pea, e takahi rawa, moe mai r ā koutou ki te uru. Tēnei ka rere a Te Papa Tongarewa whakamua ki ng ā whakawai o te wā. -
Effects of Algal Phenotype on Mesograzer Feeding
Vol. 490: 69–78, 2013 MARINE ECOLOGY PROGRESS SERIES Published September 17 doi: 10.3354/meps10429 Mar Ecol Prog Ser Effects of algal phenotype on mesograzer feeding Edwin Cruz-Rivera1,3,*, Michael Friedlander2 1Department of Biology, The American University in Cairo, AUC Avenue, PO Box 74, New Cairo 11835, Egypt 2Israel Oceanographic and Limnological Research Institute, Haifa 31080, Israel 3Present address: Environmental Science Program, Asian University for Women, 20/A M. M. Ali Road, Chittagong, Bangladesh ABSTRACT: The consequences of intraspecific variation in prey traits for plant−herbivore interac- tions were tested by measuring the susceptibility of 3 phenotypes from the red alga Gracilaria cornea against herbivores from the coast of Israel. The 3 algal phenotypes (‘fine’, ‘green’, ‘wild’) differed in morphology, as well as nutritional value (organic content). When presented with the 3 G. cornea phenotypes simultaneously, the amphipod Ampithoe ramondi and the crab Acanthonyx lunulatus consumed significantly more of the finely branched phenotype (63 and 80% of total con- sumption, respectively) than of either the green or wild phenotypes. When confined with only 1 of the 3 algal phenotypes, feeding patterns of the crab changed little, consuming significantly more of the finely branched phenotype. In contrast, the amphipod responded by increasing consump- tion proportionally on the phenotypes with the lowest organic content. Regression analysis showed that A. ramondi exhibited compensatory feeding and consumed significantly more of the green phenotype than of either of the other 2 under no-choice conditions, with algal ash-free dry mass explaining approximately 83% of the variance in feeding for this mesograzer. Data suggest that feeding by crabs responded to algal morphology more, while amphipods cued on both struc- ture and nutrient content of the algal phenotypes.