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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. -
The Current Status of Halophila Beccarii: an Ecologically Significant, Yet Vulnerable
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 5 August 2020 doi:10.20944/preprints202008.0126.v1 The current status of Halophila beccarii: An ecologically significant, yet Vulnerable seagrass of India 1Amrit Kumar Mishra, 1Deepak Apte 1Marine Conservation Department, Bombay Natural History Society, Hornbill House, Dr. Salim Ali Chowk, Shaheed Bhagat Singh Road, Opp. Lion Gate, Mumbai, 400001, India Corresponding author: [email protected] Abstract: We reviewed the current status of a Vulnerable seagrass, Halophila beccarii from the coast of India using the published data from 1977-2020. We found that the seagrass, H. beccarii has a pan India distribution on both east and west coast. It is abundant in the intertidal silty-muddy region on the west coast, while on the east coast it is found on sandy habitats, with few exceptions of muddy habitat. H. beccarii was found to be associated with mangroves or smaller seagrass species within a depth limit of 1.7m. Low salinity and high nitrate levels were observed for the H. beccarii meadows of the west coast due to its association with mangroves. The nutrient levels in H. beccarii meadows of India were comparatively lower than other seagrass meadows. Most of the research on H. beccarii has focoused on its morphometrics (41%), reproductive (33%) and distribution (29%) along the coast of India. Reproductive traits such as flowering and fruiting varying according to the seasons of each coast due to the influence of monsoon and its associated temperature, salinity and nutrient influx. H. beccarii has a great potential of various bioactive compounds, which needs further investigation. -
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. -
Seagrasses from the Philippines
SMITHSONIAN CONTRIBUTIONS TO THE MARINE SCIENCES •NUMBER 21 Seagrasses from the Philippines Ernani G. Mefiez, Ronald C. Phillips, and Hilconida P. Calumpong ISSUED DEC 11983 SMITHSONIAN PUBLICATIONS SMITHSONIAN INSTITUTION PRESS City of Washington 1983 ABSTRACT Menez, Ernani G., Ronald C. Phillips, and Hilconida P. Calumpong. Sea grasses from the Philippines. Smithsonian Contributions to the Marine Sciences, number 21, 40 pages, 26 figures, 1983.—Seagrasses were collected from various islands in the Philippines during 1978-1982. A total of 12 species in seven genera are recorded. Generic and specific keys, based on vegetative characters, are provided for easier differentiation of the seagrasses. General discussions of seagrass biology, ecology, collection and preservation are presented. Local and world distribution of Philippine seagrasses are also included. OFFICIAL PUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution's annual report, Smithsonian Year. SERIES COVER DESIGN: Seascape along the Atlantic coast of eastern North America. Library of Congress Cataloging in Publication Data Menez, Ernani G. Seagrasses from the Philippines. (Smithsonian contributions to the marine sciences ; no. 21) Bibliography: p. Supt. of Docs, no.: SI 1.41:21 1. Seagrasses—Philippines. I. Phillipps, Ronald C. II. Calumpong, Hilconida P. III. Ti tle. IV. Series. QK495.A14M46 1983 584.73 83-600168 Contents Page Introduction 1 Acknowledgments 3 Materials and Methods 3 Collecting and Preserving Seagrasses 4 General Features of Seagrass Biology and Ecology 6 Key to the Philippine Seagrasses 7 Division ANTHOPHYTA 8 Class MONOCOTYLEDONEAE 8 Order HELOBIAE 8 Family POTAMOGETONACEAE 8 Cymodocea rotundata Ehrenberg and Hemprich, ex Ascherson 8 Cymodocea serrulata (R. -
Reproductive Biology of the Tropical-Subtropical Seagrasses of the Southeastern United States
Reproductive Biology of the Tropical-Subtropical Seagrasses of the Southeastern United States Mark D. Moffler and Michael J. Durako Florida Department of Natural Resources Bureau of Marine Research 100 Eighth Ave., S.E. St. Petersburg, Florida 33701 ABSTRACT Studiesof reproductivebiology in seagrassesof the southeasternUnited States have addressed descriptive morphologyand anatomy,reproductive physiology, seed occurrence,and germination.Halodale wrightii Aschers.,Halophila engelmannii Aschers., Syringodium filiforme Kutz., and Thalassiatestudiaum Banks ex Konig are dioecious;Halophila decipiens Ostenfeld and Ruppiamaritima L. are monoecious.In Halophila johrtsoaii Eiseman, only fernale flowers are known. With the exception of R, maritima, which has hydroanemophilouspollination, these species have hydrophilous pollination. Recent reproductive-ecology studiessuggest that reproductivepatterns are due to phenoplasticresponses and/or geneticadaptation to physico-chemicalenvironmental conditions. Laboratory and field investigationsindicate that reproductive periodicityis temperaturecontrolled, but proposedmechanisms are disputed.Water temperature appears to influencefloral developmentand maybe importantin determiningsubsequent flower densities and fruit/seed production.Flowering under continuouslight in vitro suggeststhat photoperiodplays a limitedrole in floral induction.Flower expression and anthesis,however, may be influencedby photoperiod.Floral morpho- ontogeneticstudies of T. testudinumfield populationsdemonstrated the presenceof early-stageinflorescences -
Reproductive Effort of Intertidal Tropical Seagrass As an Indicator of Habitat Disturbance
bioRxiv preprint doi: https://doi.org/10.1101/2020.07.19.177899; this version posted July 19, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Reproductive effort of intertidal tropical seagrass as an indicator of habitat disturbance 2 1Amrit Kumar Mishra, 1Deepak Apte 3 1Marine Conservation Department, Bombay Natural History Society, Hornbill House, Dr. 4 Salim Ali Chowk, Shaheed Bhagat Singh Road, Opp. Lion Gate, Mumbai, 400001, India 5 Corresponding author: [email protected] 6 Abstract: 7 Habitat disturbance is one of the major causes of seagrass loss around the Andaman Sea in 8 the Indian Ocean bioregion. Assessing the seagrass response to these disturbances is of 9 utmost importance in planning effective conservation measures. Here we report about 10 seagrass reproductive effort (RE) as an indicator to assess seagrass response to habitat 11 disturbances. Quadrat sampling was used to collect seagrass samples at three locations (a 12 disturbed and undisturbed site per location) of the Andaman and Nicobar Islands. The health 13 of seagrass meadows was quantified based on density-biomass indices of the disturbed sites. 14 A change ratio (D/U) was derived by contrasting the RE of disturbed (D) sites with the 15 undisturbed (U) sites of all three locations. The relationship between RE and plant 16 morphometrics were also quantified. Reproductive density of T. hemprichii was higher and 17 significant at the three disturbed sites. -
Seagrass Meadows - Encyclopedia of Earth
Seagrass meadows - Encyclopedia of Earth http://www.eoearth.org/article/Seagrass_meadows Encyclopedia of Earth Seagrass meadows Lead Author: Carlos M. Duarte (other articles) Article Topics: Oceans and Marine ecology This article has been reviewed and approved by the following Topic Table of Contents Editor: Jean-Pierre Gattuso (other articles) 1 Introduction Last Updated: September 21, 2008 2 Adaptations to Colonize the Sea 3 Seagrass Distribution and Habitat 4 Seagrass Functions 5 Conservation Issues Introduction 6 Further Reading Seagrasses are angiosperms that are restricted to life in the sea. Seagrasses colonized the sea, from terrestrial angiosperm ancestors, about 100 million years ago, which indicates a relatively early appearance of seagrasses in angiosperm evolution. With a rather low number of species (about 50-60), seagrass comprise < 0.02% of the angiosperm flora. Seagrasses are assigned to two families, Potamogetonaceae and Hydrocharitaceae, encompassing 12 genera of angiosperms containing about 50 species (Table 1). Three of the genera, Halophila , Zostera and Posidonia , which may have evolved from lineages that appeared relatively early in seagrass evolution, comprise most (55%) of the species, while Enhalus , the most recent seagrass genus, is represented by a single species ( Enhalus acoroides , Photo 1: Posidonia oceanica meadow in the NW Table 1). Most seagrass meadows are monospecific, but Mediterranean. (Photograph by M. Sanfélix) may develop multispecies, with up to 12 species, meadows in subtropical and tropical waters. Adaptations to Colonize the Sea The colonization of the sea required a number of key adaptations including (1) blade or subulate leaves with sheaths, fitted for high-energy environments; (2) hydrophilous pollination, allowing submarine pollination (except for the genus Enhalus ) and subsequent propagule dispersal; and (3) extensive lacunar systems allowing the internal gas flow needed to maintain the oxygen supply required by their below-ground structures in anoxic sediments. -
Of the Red Sea
SeagrassesField Guide to of the Red Sea By Amgad El Shaffai Edited by: Anthony Rouphael, PhD Ameer Abdulla, PhD SeagrassesField Guide to of the Red Sea Text and Photographs by Amgad El Shaffai Edited by: Anthony Rouphael, PhD Ameer Abdulla, PhD The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN, concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN. Published by: IUCN, Gland, Switzerland and Total Foundation, Courbevoie, France. Copyright: © 2011 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other noncommercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: El Shaffai, A. (2011). Field Guide to Seagrasses of the Red Sea. Rouphael, A. and Abdulla, A., eds. First Edition. Gland, Switzerland: IUCN and Courbevoie, France: Total Foundation. viii + 56pp. ISBN: 978-2-8317-1414-1 This publication is a contribution of the Marine Biodiversity and Conservation Science Group. Design and layout: Tasamim Design - www.tasamim.net Cover picture: Amgad El Shaffai All photographs used in this publication remain the property of the original copyright holder. Photographs should not be reproduced or used in other contexts without written permission from the copyright holder. -
Influence of the Seagrass Thalassia Hemprichii on Coral Reef Mesocosms Exposed to Ocean Acidification and Experimentally Elevate
Science of the Total Environment 700 (2020) 134464 Contents lists available at ScienceDirect Science of the Total Environment journal homepage: www.elsevier.com/locate/scitotenv Influence of the seagrass Thalassia hemprichii on coral reef mesocosms exposed to ocean acidification and experimentally elevated temperatures a,b c b,1 c, Pi-Jen Liu , Shin-Jing Ang , Anderson B. Mayfield , Hsing-Juh Lin ⇑ a Graduate Institute of Marine Biology, National Dong-Hwa University, Pingtung 94450, Taiwan b National Museum of Marine Biology and Aquarium, Pingtung 94450, Taiwan c Department of Life Sciences and Innovation and Development Center of Sustainable Agriculture, National Chung Hsing University, Taichung 40227, Taiwan highlights graphical abstract The combined effect of OA and rising Conceptual model of climate change (ocean acidification [OA] and seawater warming) effects on coral temperatures stimulated the growth reef mesocosms that either do (light blue) or do not (blue) feature seagrass beds. Solid lines denote abi- of macroalgae. otic effects (i.e., OA or OA + warming to 31C), whereas dotted lines depict effects of co-incubation with OA resulted in higher coral seagrass. CCM = carbon concentrating mechanism. ER=ecosystem respiration, GPP = gross primary pro- calcification rates when corals were duction, NEP = net ecosystem metabolism, and P/R = photosynthesis/respiration ratio. co-incubated with seagrass. Macroalgal growth was lower in seagrass-containing mesocosms. Coral and macroalgal, but not seagrass, growth suffered at 31 °C under OA conditions. Seagrass helped to stabilize the system’s metabolism in response to projected climate change stressors. article info abstract Article history: Ocean acidification (OA) and warming currently threaten coastal ecosystems across the globe. -
Managing Seagrasses for Resilience to Climate Change
Managing Seagrasses for Resilience to Climate Change Mats Björk, Fred Short, Elizabeth Mcleod and Sven Beer IUCN Resilience Science Group Working Paper Series - No 3 IUCN Global Marine Programme Founded in 1948, IUCN brings together States, government agencies and a diverse range of non-governmental organizations in a unique world partnership: over 1000 members in all, spread across some 140 countries. As a Union, IUCN seeks to influence, encourage and assist societies throughout the world to conserve the integrity and diversity of nature and to ensure that any use of natural resources is equitable and ecologically sustainable. The IUCN Global Marine Programme provides vital linkages for the Union and its members to all the IUCN activities that deal with marine issues, including projects and initiatives of the Regional offices and the 6 IUCN Commissions. The IUCN Global Marine Programme works on issues such as integrated coastal and marine management, fisheries, marine protected areas, large marine ecosystems, coral reefs, marine invasives and protection of high and deep seas. The Nature Conservancy The mission of The Nature Conservancy is to preserve the plants, animals and natural communities that represent the diversity of life on Earth by protecting the lands and waters they need to survive. The Conservancy launched the Global Marine Initiative in 2002 to protect and restore the most resilient examples of ocean and coastal ecosystems in ways that benefit marine life, local communities and economies. The Conservancy operates over 100 marine conservation projects in more than 21 countries and 22 US states; we work with partners across seascapes and landscapes through transformative strategies and integrated planning and action. -
Seagrasses of the Great Barrier Reef JANET LANYON
Seagrasses of the Great Barrier Reef JANET LANYON IIE.strallorls Geo~f Kelly ~.~.~,.Great Barrier Ree| Marine Park Authority ~'Special PubJication Series (3) Guide to the Identification of Seagrasses in the Great Barrier Reef Region JANET LANYON Illustrations Geoff Kelly ~ Great Barrier Reef Marine Park Authority Special Publication Series (3) ISSN 0810--6983 ISBN 0--642--52489--0 Cover Design: Geoff Kelly NOTES ABOUT THE AUTHOR Janet Lanyon is currently doing a PhD in Zoology with supervisors at both Monash and James Cook Universities. Her interest in seagrass stems from research in which she is examining seagrass as food for dugongs. In addition to monitoring seasonal changes in the seagrass meadows of the Townsville region, Janet has been involved in seagrass surveys within the Great Barrier Reef Marine Park and Torres Strait. Her other interests include nutritional biology and ecology, particularly of Australian mammals, plant-herbivore relationships, marine mammal biology and various aspects of reef ecology. Published by GBRMPA 1986 Typesetting and artwork: Tim Weaver Graphics, Townsville, Queensland. Printed by Nadicprint Services Pty. Ltd., Townsville, Queensland. ACKNOWLEDGEMENTS I wish to thank the following people for their valuable comments and criticism of the manuscript: Dr. Helene Marsh, Dr. Gordon Sanson, Mark Simmons, Dr. lan Price, Dr. Tony Larkum, Robert Coles, Dr Peter Arnold and Ruth Lanyon. Thanks must also go to Bey and Lyle Squire and Warren Lee Long of Queensland Fisheries, Cairns, for providing additional seagrass specimens, and to the seagrass workshop participants who attempted and commented on the taxonomic keys. I am most grateful to both Dr. lan Poiner of CSIRO Marine Laboratories, and the Great Barrier Reef Marine Park Authority for allowing me to participate in recent northern Australian seagrass surveys. -
Seagrasses and Eutrophication
Seagrasses and eutrophication Interactions between seagrass photosynthesis, epiphytes, macroalgae and mussels Esther Francis Mvungi ©Esther F. Mvungi, Stockholm 2011 Front cover: Photo showing eutrophic seagrass bed in the Western Indian Ocean. Photo: Mats Björk ISBN 978-91-7447-250-9 Printed in Sweden by Universitetservice, US-AB, Stockholm 2011 Distributor: Department of Botany, Stockholm University To my husband, Denis and my daughter, Doreen Abstract Seagrass meadows are highly productive, ecologically and economically valuable ecosystems. However, increased human activities along the coastal areas leading to processes such as eutrophication have resulted in the rapid loss and deterioration of seagrass ecosystems worldwide. This thesis focuses on the responses of seagrasses to increases in nutrients, subsequent increases in ephemeral algae, and changes in the physical- chemical properties of seawater induced by interaction with other marine biota. Both in situ and laboratory experiments conducted on the tropical seagrasses Cymodocea serrulata and Thalassia hemprichii revealed that increased concentrations of water column nutrients negatively affected seagrass photosynthesis by stimulating the growth of the epiphytic biomass on the seagrass leaves. Interaction between seagrasses and other marine organisms induced different responses in seagrass photosynthesis. Ulva intestinalis negatively affected the photosynthetic performance of the temperate seagrass Zostera marina both by reducing the light and by increasing the pH of the surrounding water. On the other hand, the coexistence of mussels Pinna muricata and seagrass Thalassia hemprichii enhanced the photosynthetic activity of the seagrass, but no effect on the mussels’ calcification was recorded. This study demonstrates that seagrass productivity is affected by a multitude of indirect effects induced by nutrient over-enrichment, which act singly or in concert with each other.