The Ichthyofauna Associated with Zostera Capensis Setchell Ill the Swartkops Estuary, South Africa

Total Page:16

File Type:pdf, Size:1020Kb

The Ichthyofauna Associated with Zostera Capensis Setchell Ill the Swartkops Estuary, South Africa The ichthyofauna associated with Zostera capensis Setchell ill the Swartkops estuary, South Africa Lynnath E. Beckley Department of Zoology, University of Port Elizabeth The ichthyofauna associated with Zostera beds in the lower Studies on the ichthyofauna of the Swartkops estuary near reaches of the Swartkops estuary was examined by means of Port Elizabeth (33°S8'SI2S037'E) have recently been under­ haul seine netting over 15 months. Thirty-nine fish species were caught In the Zostera beds and the small shoaling taken to follow up the pioneer surveys by Gilchrist (1918). species, Hepsetis. "'reviceps and Gilchrlstella aestuarius, con­ Work by Winter (1979), Marais & Baird (1980a, b) and stituted 55% of the t\..~'31 catch In terms of numbers. Juveniles Melville-Smith & Baird (1980) has provided information on of six mullet species occurred in the Zostera and recruitment the species composition, seasonal abundance and size fre­ took place throughout the year. Sparlds such as Rhabdosargus holubi and Dlplodus sargus showed marked spring and sum­ quency distribution of the adult, juvenile and larval fish oc­ mer recruitment. The recruitment patterns of Juveniles to the curring in the main channel of the estuary. Zostera beds is correlated with documented breeding cycles of Two relatively large creeks, Modderspruit and Tippers adults, particularly those breeding in the shallow inshore Creek, are located in the lower reaches of the 16-km long marine environment. The Swartkops Zostera beds were found to form an integral and important part of the nursery function Swartkops estuary (Figure 1). The creeks support about 9 ha of the estuary. (B. Talbot, pers. comm.) of the seagrass Zostera capensis. S. Afr. J. Zool. 1983, 18: 15 - 24 The importance of seagrasses such as Zostera, Posidonia ) 0 and Thalassia as nursery areas for juvenile fish is well 1 0 Die visgemeenskap in die Zostera-beddens van die Swartkops­ documented (Adams 1976; Weinstein & Heck 1979; Young 2 riviermonding is deur middel van treknetvangste oor 15 maande d 1981) and is emphasized by Kikuchi (1980) in his review of e bestudeer. Nege-en-dertig spesles Is gevang en 55% van die t a aantal vis wat gevang is, het ult die twee spesles Hepsetia faunal relationships in temperate seagrass beds. d ( breviceps en Gilchristel/a aestuarlus bestaan. Klein- The present study was aimed at determining the r tjies van ses Mugllidae-spesies het in die Zostera voorgekom e significance of Zostera beds in the Swartkops estuary as h en rekrutering het gedurende die hele jaar plaasgevlnd. s i nursery areas for juvenile fish and thereby supplementing l Sparidae soos Rhabdosargus holubl en Diplodus sargus het b the results of earlier workers who did not effectively sam­ u rekrutering gedurende lente en somer vertoon. Die rekruter­ P ingspatroon van klein vissies tot die Zostera-beddens Is gekor­ ple the vegetated creeks of the lower reaches. The study e releer met gedokumenteerde teelsiklusse van volwassenes, in h t forms part of a comparative programme on juvenile marine besonder, die spesies wat in die vlak kuswaters voortplant. Ole y fish in estuaries and the nearshore coastal region. Concur­ b stu die het bewys dat die Swartkops Zostera-beddens 'n in­ d tegrale en belangrike deel van die kweekfunksie van die rent with the present study were investigations of the in­ e t getyrlvler uitmaak. vertebrates associated with beds in the Swartkops n Zostera a S.-Afr. Tydskr. Dierlc. 1983, 18: 15 - 24 r estuary (Nusch 1981; Emmerson, Watling & Watling 1982) g e and the Kromme estuary (Hanekom 1982). c n e c i l Methods r e Fish were collected monthly from January 1980 through d n March 1981 by means of a small haul-seine net (10,5 m x u y 2,5 m) with a stretched mesh size of 2 mrn. At low tide a a haul covering about 60 m2 was made through the w Zostera e t at each of two stations in Tippers Creek and at one station a G in Modderspruit (Figure 1). A further haul was made in an t e area with no subtidal Zostera along the bank of the main n i b channel of the estuary between the two creeks. Surface-water a S temperature and salinity were measured in the creeks on each y b sampling occasion. d L)'llDllth E. BecIdey Catches were kept frozen until sorted, identified and e c Department of Zoology, University of Port Elizabeth, u counted, and total lengths of specimens measured in mm. d P.O. Box 1600, Port Elizabeth 6000, Republic of South Africa o As the small shoaling species Hepsetia breviceps (Cuvier) r p Received 24 May 1982; accepted 20 September 1982 and Gi/christella aestuarius (Gilchrist) were the subject of e R 16 S.-Afr. Tydskr. Dierk. 1983, 18(1) a 1 K081 Bay 2 St. Lucia 3 W. Klalmond 4 Kromma 5 KnY8na 6 K lain (Harmanu8) 7 Mllnarton b Tippers Creek SWARTKOPS ESTUARY . f1pre) 1 (a) Map of Southern Africa showing the geographical position of the Swartkops estuary and other areas mentioned in the text. (b) The middle 0 and1 lower reaches of the Swartkops estuary showing the sampling stations in the creeks (1-3) and channel (4). 0 2 d e 26 at separate study by Talbot (1982) only a subsample of 100 a specimensd of these two species was measured from each sta­ ( • • tionr each month. Juvenile mullet were identified from den­ 0 0 e 24 h .. tition characteristics (van der Elst & Wallace 1976) but as 0\ s \ i itl often proved difficult to identify mullet of less than 30 mm \ b (.) \ withu confidence all mullet of this size class were grouped . • P W 22 ~--\ /0 • \ I e a: 0 together. ::::I \ / h \ / t I- 0« \ / I y a: \ / Resultsb W \ 20 I CL \ d \ I Modderspruite and Tippers Creek in the lower reaches of the :::i: I t W \ 0 Swartkopsn estuary experience sernidiurnal tides with a mean I- \ /. a \ I r 18 \ • I springg range of 1,6 m (Beckley & McLachlan 1979) and a \ 0 /0 e \ • timec lag of about 1 h after predicted times for Algoa Bay. \ ,...-0, ./ n \/ '", Salinitye varies from 30 - 35°/00 except after heavy rains. As c 16 i l the creeks are shallow « 2 m depth) water temperature is r variablee and often differs considerably from that of the main d channeln of the estuary and the adjacent sea (Figure 2). u J F M A M J J A SON D y Haul seining proved to be an effective sampling techni­ a MONTHS quew for juvenile fish as during the IS-month study period, e 62t 020 fish were caught at the three Zostera stations and a Fillure 2 Water temperatures measured in Modderspruit ( .) and Tippers G 4371 at the channel station. Mean catch per haul was I 328 Creek (0) during the study period compared with mean monthly water t (SEe ± 296) fish for the Zostera stations and only 291 (SE temperature for the lower reaches of the estuary (. ____ after Marais & n i Baird 1980b) and Algoa Bay (__ after Beckley & Mclachlan 1979). ±b 43) fish at the channel station. Total combined catch per a monthS for the three Zostera stations varied greatly, rang­ y ingb from 481 to 11 437 fish depending largely on the catch ofd the small shoaling species H. breviceps (Figure 3). the Zostera, giving a total of 43 species caught during the e c u Thirty-nine species were recorded from the creek stations study period. The number of species captured in the Zostera d ando 30 species from the channel station (Table 1). Four each month varied between 12 and 28 with more species be­ r speciesp recorded in the channel area were not captured in ing caught in the summer months (Figure 3). e R S. Afr. J. Zool. 1983, 18(1) 17 12000~------------------------------------------------~30 rn J: w <.) I­ <3 < 8000 20~ <.) rn ...J < o I- a: o 4000 10 w I- ID ::E ::J Z JFMAMJJASONDJ FM MONTHS Figure 3 Total monthly catch by seine netting at the three Swartkops creek Zostera stations (. ---.) and total number of species captured in the Zostera each month (0----0). Table 1 List of fish species captured by haul seine netting during 1980/81 in the lower reaches of the Swart­ kops estuary. Lengths given in mm, Z indicates occurrence in Zostera beds and C indicates occurrence at the channel station. Species Length range J F M A M J J A SON D J F M Ambassis natalensis Gilchrist & Thompson 17 Z 22 C Amblyrhynchotes honckenii (Bloch) 21- 32 Z Z Z 23- 77 C C C Arothron hispidus (Lacepede) 34- 54 Z Z Arothron immaculatus (Bloch-Schneider) 15 - 25 Z Caffrogobius multifasciatus (Smith) 12-102 Z Z Z Z Z Z Z Z Z Z Z Z Z Z Z 13- 61 C C C C C C C C C C C C C C . ) Clinus superciliosus (Linnaeus) 26- 81 Z Z Z Z 0 1 38- 98 C C C 0 2 Diplodus cervinus (Valenciennes) 9- 80 Z Z Z Z Z Z Z Z d e 9- 41 C C C C t a Diplodus sargus Linnaeus 10-134 Z Z Z Z Z Z Z Z Z Z Z Z Z Z d ( C C C C C C C C r 10- 93 e h Engraulis capensis Gilchrist 36 C s i l Epinephelus guaza (Linnaeus) 57 Z b u Etrumeus teres (Dekay) 31- 36 C P Gilchristella aestuarius (Gilchrist) 17- 50 Z Z Z Z Z Z Z Z Z Z Z Z Z Z Z e h t 27- 52 C C C C C C C C y Hepsetia breviceps (Cuvier) 12- 68 Z Z Z Z Z Z Z Z Z Z Z Z Z b Z Z d 12- 75 C C C C C C C C C C C e t Jleteromycteris capensis Kaup 7- 44 Z Z Z Z Z Z Z Z Z Z Z Z Z Z Z n a r 8- 56 C C C C C C C C C C C C C C C g Lichia amia (Linnaeus) 46- 98 Z Z e c n Lithognathus mormyrus (Linnaeus) 68 C e c Liza dumerili (Steindachner) 13-221 Z Z Z Z Z Z Z Z Z Z Z Z Z i l r 11-237 C C C C C C C e d Liza richardsoni (Smith) 11-160 Z Z Z Z Z Z Z Z Z Z Z Z n u 28-180 C C C y Lizo tricuspidens (Smith) 17 -116 Z Z Z Z Z Z Z Z Z Z Z Z a w 29-126 C C C C C C C e t Lophodiodon calori (Bianconi) Z a 11 G Lutjanus lulvif7amma (Forsskiil) 17- 21 Z Z t e Monodactylus falciformes (Lacepede) 7- 28 Z Z Z Z n i b 11- 17 C a S Mugil cephalus Linnaeus 7-153 Z Z Z Z Z Z Z Z Z Z Z Z y 8-172 C C C C C C C C C b d Myxus capensis (Valenciennes) 24- 29 Z Z e c Omobranchus woodi (Gilchrist & Thompson) 19- 20 Z Z u d 18- 19 C C o r p Pelates quadrilineatus (Bloch) 22 Z e R 18 S.-Afr.
Recommended publications
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • Whitfield Et Al. 2017.Pdf
    Biological Conservation 212 (2017) 256–264 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Life-histories explain the conservation status of two estuary-associated MARK pipefishes ⁎ Alan K. Whitfielda, , Thomas K. Mkareb,1, Peter R. Teskeb, Nicola C. Jamesa, Paul D. Cowleya a South African Institute for Aquatic Biodiversity (SAIAB), Private Bag 1015, Grahamstown 6140, South Africa b Molecular Zoology Laboratory, Department of Zoology, University of Johannesburg, Aukland Park 2006, South Africa ABSTRACT Two endemic southern African pipefish species (Teleostei: Syngnathidae) co-occur in estuaries on the southeast coast of South Africa. The larger longsnout pipefish, Syngnathus temminckii, is abundant and has a wide range that comprises coastal and estuarine habitats in all three of the region's marine biogeographic provinces. In contrast, the smaller estuarine pipefish S. watermeyeri is critically endangered, and confined to a few warm- temperate estuaries. Here, we explore reasons for these considerable differences in conservation status. Fecundity is related to fish size, with large live-bearing S. temminckii males carrying up to 486 developing eggs/ embryos, compared to a maximum of only 44 recorded for S. watermeyeri. Loss of submerged seagrass habitats due to episodic river flooding appears to be correlated with the temporary absence of both species from such systems. Prolonged cessation in river flow to estuaries can cause a collapse in estuarine zooplankton stocks, a food resource that is important to pipefish species. The greater success of S. temminckii when compared to S. watermeyeri can be attributed to the former species' wider geographic distribution, fecundity, habitat selection and ability to use both estuaries and the marine environment as nursery areas.
    [Show full text]
  • The Botanical Importance Rating of the Estuaries in Former Ciskei / Transkei
    THE BOTANICAL IMPORTANCE RATING OF THE ESTUARIES IN FORMER CISKEI / TRANSKEI B.M. COLLOTY, J.B. ADAMS AND G.C. BATE FINAL REPORT TO THE WATER RESEARCH COMMISSION BY THE DEPARTMENT OF BOTANY UNIVERSITY OF PORT ELIZABETH WRC REPORT NO. TT 160/01 Obtainable from: Water Research Commission PO Box 824 Pretoria 0001 The publication of this report emanates from a project entitled: The Botanical Importance rating of Estuaries in former Ciskei and Transkei (WRC Project No K5/812) DISCLAIMER This report has been reviewed by the Water Research Commission (WRC) and approved for publication. Approval does not signify that the contents necessarily reflect the views and policies of the WRC, nor does mention of trade names or commercial products constitute ensoresement or recommendation for use. ISBN 1 86845 790 7 Printed in the Republic of South Africa ii The Jujura Estuary, one of several unique estuaries observed in this study. This small estuary had an above average depth of 2.8 m, remained open for extensive periods and was colonized by Zostera capensis. iii EXECUTIVE SUMMARY BACKGROUND AND MOTIVATION FOR THE RESEARCH There are an increasing number of people utilising the South African coastline. This is creating a need to evaluate estuary and coastal resources and to identify sensitive areas where careful planning and management must take place. Management tools such as importance rating systems and state or condition assessments have become necessary to summarise and express scientific information. The botanical importance rating system is one such method and was developed in a previous Water Research Commission Project (Adams et al.
    [Show full text]
  • Estrutura E Conectividade Trófica Das Assembleias De Peixes Em Um Estuário Subtropical E Seus Sistemas Fluvial E Marinho Adjacentes
    Universidade Federal do Rio Grande 3 Instituto de Ciências Biológicas Pós-graduação em Biologia de Ambientes Aquáticos Continentais Estrutura e conectividade trófica das assembleias de peixes em um estuário subtropical e seus sistemas fluvial e marinho adjacentes Adna Ferreira Silva Garcia Orientador: João Paes Vieira Rio Grande 2018 i Universidade Federal do Rio Grande Instituto de Ciências Biológicas Pós-graduação em Biologia de Ambientes Aquáticos Continentais Estrutura e conectividade trófica das assembleias de peixes em um estuário subtropical e seus sistemas fluvial e marinho adjacentes Aluno: Adna Ferreira Silva Garcia Orientador: João Paes Vieira Tese apresentada ao Programa de Pós- graduação em Biologia de Ambientes Aquáticos Continentais como requisito parcial para a obtenção do título de Doutora em Biologia de Ambientes Aquáticos Continentais. Rio Grande 2018 ii A todos que se fizeram presente em momentos especiais da minha vida, em especial a Adnaldo e Elizabete (meus pais), Edriene e Edyclênia (minhas irmãs), Thaieny e Ezequias (meus sobrinhos) e Alexandre (meu esposo) pelo amor, carinho, união e por fazer com que suas presenças me mantivessem sempre confiante, dedico. iii AGRADECIMENTOS À CAPES pelo apoio financeiro com a bolsa de pós-graduação e doutorado sanduíche a mim concedida. À FAPERGS e ao CNPq pelo apoio financeiro nas expedições a campo e análise dos isótopos estáveis. À FURG, ao Centro de Estudos Costeiros, Limnológicos e Marinhos (CECLIMAR - UFRGS) e as instalações do Laboratório de Ictiologia - IO pelo apoio logístico para a execução da tese. Ao Programa de Pós-Graduação em Biologia de Ambientes Aquáticos Continentais (PPGBAC) e ao seu Corpo Docente pela excelência em formação de pessoal.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • The Genus Ruppia L. (Ruppiaceae) in the Mediterranean Region: an Overview
    Aquatic Botany 124 (2015) 1–9 Contents lists available at ScienceDirect Aquatic Botany journal homepage: www.elsevier.com/locate/aquabot The genus Ruppia L. (Ruppiaceae) in the Mediterranean region: An overview Anna M. Mannino a,∗, M. Menéndez b, B. Obrador b, A. Sfriso c, L. Triest d a Department of Sciences and Biological Chemical and Pharmaceutical Technologies, Section of Botany and Plant Ecology, University of Palermo, Via Archirafi 38, 90123 Palermo, Italy b Department of Ecology, University of Barcelona, Av. Diagonal 643, 08028 Barcelona, Spain c Department of Environmental Sciences, Informatics & Statistics, University Ca’ Foscari of Venice, Calle Larga S. Marta, 2137 Venice, Italy d Research Group ‘Plant Biology and Nature Management’, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels, Belgium article info abstract Article history: This paper reviews the current knowledge on the diversity, distribution and ecology of the genus Rup- Received 23 December 2013 pia L. in the Mediterranean region. The genus Ruppia, a cosmopolitan aquatic plant complex, is generally Received in revised form 17 February 2015 restricted to shallow waters such as coastal lagoons and brackish habitats characterized by fine sediments Accepted 19 February 2015 and high salinity fluctuations. In these habitats Ruppia meadows play an important structural and func- Available online 26 February 2015 tional role. Molecular analyses revealed the presence of 16 haplotypes in the Mediterranean region, one corresponding to Ruppia maritima L., and the others to various morphological forms of Ruppia cirrhosa Keywords: (Petagna) Grande, all together referred to as the “R. cirrhosa s.l. complex”, which also includes Ruppia Aquatic angiosperms Ruppia drepanensis Tineo.
    [Show full text]
  • 10 Lockyear.Qxp
    African Journal of Aquatic Science 2006, 31(2): 275–283 Copyright © NISC Pty Ltd Printed in South Africa — All rights reserved AFRICAN JOURNAL OF AQUATIC SCIENCE EISSN 1727–9364 The distribution and abundance of the endangered Knysna seahorse Hippocampus capensis (Pisces: Syngnathidae) in South African estuaries Jacqueline F Lockyear1, Thomas Hecht1, Horst Kaiser1* and Peter R Teske2 1 Department of Ichthyology and Fisheries Science, Rhodes University, PO Box 94, Grahamstown 6140, South Africa 2 Molecular Ecology and Systematics Group, Botany Department, Rhodes University, PO Box 94, Grahamstown 6140, South Africa * Corresponding author, e-mail: [email protected] Received 7 July 2005, accepted 23 March 2006 The occurrence, distribution and abundance of the endangered Knysna seahorse Hippocampus capensis in 10 estuaries on South Africa’s warm temperate south coast, were investigated. Seahorses were found only in the Knysna, Swartvlei and Keurbooms estuaries. Sex ratios were even and, in most cases, more adults were found than juveniles. During the first year of study, seahorse densities were higher in the Swartvlei and Keurbooms estuaries than in the comparatively larger Knysna Estuary but, during the second year, seahorses were absent from the Keurbooms estuary, and the population size in the Swartvlei Estuary had decreased by more than 80%. These results suggest that, although the two smaller estuaries are able to support comparatively high densities of seahorses, population sizes may fluctuate considerably. Population size estimates for the Knysna Estuary were similar to those obtained in a previous study, suggesting that this estuary may represent a more stable environment and may thus be particularly important for the survival and conservation of this species.
    [Show full text]
  • The Effects of Hypersalinity on the Growth and Skeletal Anomalies of Juvenile Cape Stumpnose, Rhabdosargus Holubi (Sparidae)
    SCIENTIA MARINA 83(1) March 2019, 61-68, Barcelona (Spain) ISSN-L: 0214-8358 https://doi.org/10.3989/scimar.04859.24A The effects of hypersalinity on the growth and skeletal anomalies of juvenile Cape stumpnose, Rhabdosargus holubi (Sparidae) Yanasivan Kisten 1, 2, Nadine A. Strydom 2, Renzo Perissinotto 1 1 DST/NRF Research Chair in Shallow Water Ecosystems, Nelson Mandela University, Ocean Science Campus, P.O. Box 77000, Port Elizabeth 6031, South Africa. (YK) (Corresponding author) E-mail: [email protected]. ORCID iD: http://orcid.org/0000-0001-5468-0230 (RP) E-mail: [email protected]. ORCID iD: http://orcid.org/0000-0002-9224-3573 2 Department of Zoology, Nelson Mandela University, Summerstrand Campus South, P.O. Box 77000, Port Elizabeth 6031, South Africa. (NAS) E-mail: [email protected]. ORCID iD: http://orcid.org/0000-0003-4292-8678 Summary: Estuarine organisms are exposed to hypersaline conditions for prolonged periods during drought conditions and under severely restricted river flow resulting from freshwater abstraction and impoundments. Consequently, marine estuarine-dependent fish such as Rhabdosargus holubi may be subjected to extreme conditions, such as hypersalinity prevail- ing for long periods (>2 months). Hypersalinity may impact the energetic demands of fish due to osmoregulation leading to compromised growth. This study assessed the impact of high salinity on the growth and skeletal development of R. holubi juveniles. Skeletons of juveniles grown at different salinities in the wild and in aquaria were analysed for anomalies. The impact of hypersaline conditions on juvenile R. holubi growth was also determined in aquaria.
    [Show full text]
  • Thesis Sci 2020 Lawrence Cloverley Mercia.Pdf
    Ecology and Ecophysiology of Zostera capensis: Responses and Acclimation to Temperature Cloverley Mercia Lawrence Thesis presented for the degree of Doctor of Philosophy in the Department of Biological Sciences Faculty of Science University of Cape Town 2019 University of Cape Town Supervisors Dr Deena Pillay, Professor Astrid Jarre, Emer. Professor John Bolton The copyright of this thesis vests in the author. No quotation from it or information derived from it is to be published without full acknowledgement of the source. The thesis is to be used for private study or non- commercial research purposes only. Published by the University of Cape Town (UCT) in terms of the non-exclusive license granted to UCT by the author. University of Cape Town This thesis is dedicated to my parents. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Declaration I, hereby declare that all the work presented in this thesis is my original work in both concept and execution (except where otherwise indicated), and that this thesis has not been submitted in whole or in part for another degree in this or any other university. Cloverley Mercia Lawrence Table of Contents Acknowledgements………………………………………………………………………………….iii Summary.…………………………………………………………………………………………….…v Chapter One General overview and background ……………… ……... ………………………………. .. 1 1.1. Seagrass Ecosystems…………………………………………………………… …… …... 3 1.1.1. Glo bal importance and distribution of seagrasses…………………… ……... 3 1.1.2. Biodiversity in seagrass ecosystems ……………………………… ….… ….…. 6 1.2. Threats to seagrasses………………………………………………………… ….. .…. …. 8 1.2.1. The influenc e of temperature on seagrasses……………………… ……….. .. 9 1.2.2. Epiphytes and fou ling in seagrass ecosystems……………………… …….. .. 12 1.3. Respo nses of seagrasses to threats………………………………………… ….. ….. …. 12 1.3.1. Acclimations in seagrasses…… .. ………………………………… …… ….. …… 12 1.3.2.
    [Show full text]
  • Extinction Risk Assessment of the World's Seagrass Species
    Author version: Biol. Conserv.: 144(7); 2011; 1961-1971. Extinction risk assessment of the world’s seagrass species Frederick T. Short a,*, Beth Polidoro b, Suzanne R. Livingstone b, Kent E. Carpenter b, Salomao Bandeira c, Japar Sidik Bujang d, Hilconida P. Calumpong e, Tim J.B. Carruthers f, Robert G. Coles g, William C. Dennison f, Paul L.A. Erftemeijer h, Miguel D. Fortes i, Aaren S. Freeman a, T.G. Jagtap j, Abu Hena M. Kamal k, Gary A. Kendrick l, W. Judson Kenworthy m, Yayu A. La Nafie n, Ichwan M. Nasution o, Robert J. Orth p, Anchana Prathep q, Jonnell C. Sanciangco b, Brigitta van Tussenbroek r, Sheila G. Vergara s, Michelle Waycott t, Joseph C. Zieman u *Corresponding author. Tel.: +1 603 862 5134; fax: +1 603 862 1101. [email protected] (F.T. Short), a University of New Hampshire, Department of Natural Resources and the Environment, Jackson Estuarine Laboratory, 85 Adams Point Road, Durham, NH 03824, USA b IUCN Species Programme/SSC/Conservation International, Global Marine Species Assessment, Biological Sciences, Old Dominion University, Norfolk, VA 23529, USA c Universidade Eduardo Mondlane, Department of Biological Sciences, 1100 Maputo, Mozambique d Universiti Putra Malaysia Bintulu Sarawak Campus, Faculty of Agriculture and Food Sciences, Sarawak, Malaysia e Silliman University, Institute of Environmental and Marine Sciences, Dumaguete City 6200, Philippines f University of Maryland Center for Environmental Science, Cambridge, MD 21613, USA g Northern Fisheries Centre, Fisheries Queensland, Cairns, Queensland 4870, Australia h Deltares (Formerly Delft Hydraulics), 2600 MH Delft, The Netherlands i University of the Philippines, Marine Science Institute CS, Diliman, QC 1101, Philippines j National Institute of Oceanography, Donapaula, Goa-403 004, India k University of Chittagong, Institute of Marine Sciences and Fisheries, Chittagong 4331, Bangladesh l The University of Western Australia, Oceans Institute and School of Plant Biology Crawley, 6009, W.
    [Show full text]