The Genus Terpios (Suberitidae)(Suheritidae) and New Species in the «Lobiceps» Complexcomplex**

Total Page:16

File Type:pdf, Size:1020Kb

The Genus Terpios (Suberitidae)(Suheritidae) and New Species in the «Lobiceps» Complexcomplex** SCI. MAR., 57(4): 381-393 SCIENTIA MARINA 1993 RECENT ADVANCES IN ECOLOGY AND SYSTEMATICS OF SPONGES. M.J. UR1ZURIZ and K. RUTZLER (eds.).(eds.). The genus Terpios (Suberitidae)(Suheritidae) and new species in the «Lobiceps» complexcomplex** KLAUS RUTZLER and KATHLEEN P. SMITH Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution,Institution, Washington,Washington, D.C.DC. 20560, U.S.A. SUMMARY: The genus Terpios, first described from thethe Atlantic Ocean (West(West Indies)Indies) almostalmost 130 yearsyears ago,ago, isis redefined on the basis of structural studies of tylostyles and data on procaryotic symbionts.symbionts. ItsIts relationrelation toto similarsimilar generagenera in the family Suberitidae is reviewed by comparing new findings with traditionallytraditionally used characters, suchsuch asas bodybody shape,shape, skeleton arrangement, and spicule size. Two new species, T. manglaris and 7".T. belindae, areare described fromfrom shallow-shallow­ water habitats in the Caribbean Sea. They resemble Suberites lobicepslobiceps Schmidt, a poorly knownknown spongesponge fromfrom FloridaFlorida that has not been found since its first description inin 1870. Key words: Porifera, bacteria, symbiosis, Terpios, new species, Caribbean. INTRODUCTION Because of its shape and striking color, Terpios fugax is very distinctive, and the genus Terpios has In their pioneering study of Caribbean sponges, remained valid for almost 130 years, although it was DUCHASSAING and MICHELOTTI (1864:97) introduced not universally adopted. VON LENDENFELD (1897: the genus Terpios for thinly encrusting (membrani-(membrani­ 132), for example, who found the type species in the form) sponges in which the spicules are arranged hap-hap­ Adriatic, redescribedredescribedit it under the name Suberites fu-fu­ hazardly except for some organization into fan-fan­ gax.gax, However, he failed to recognize the taxonomic shaped bundles. They described nine species in four value of spicule-size classes, as they occur in Suberites live-color groups. Their diagnosis may have led Vos-Vos­ proper, and of the peculiar shape of Terpios tylos-tylos­ MAER (1887:359) to place T. fugaxfugax in this genus and tyles. The same was true of his colleague TOPSENT DE LAUBENFELS (1936a:(1936a:152) 152) to select it as the geno-geno­ (1900:(1900:192f),192f), who argued that Terpios is distinguished type,type. T. fugax not only conforms to the original defi-defi­ from Suberites by encrusting (rather than massive) nition but is the only encrusting species of the re-re­ habit, gelatin-soft consistency, a smooth surface with-with­ maining three of the original nine that are still out spicule reinforcement of the ectosome, and regu-regu­ recognizable (VAN SOEST, etai,et at" 1983:204). The other lar and loose skeleton structure. TOPSENT (1900:194)(1900: 194) two are T. aurantiaca, definitely a massive species, pointed out that the tylostyles of T. fugaxfugax are non-non­ and T. janiae,janiae, which is a Dysidea. fusiform, as the shaft progressively thins to a sharp point, and their heads are quite variable, from glob-glob­ * Received February 10, 1993. Accepted June 2, 1993. ular with tapered top to depressed, some being tri- NEWS SPECIES OF TERPIOS 381 lobed and some having annular swellingsswellings inin thethe neckneck alive and with thethe help ofof phase-contrastphase-contrast microsco­microsco- region. These observations werewere expandedexpanded uponupon byby py. Museum material was fixedfixed inin 1010 %% formalin­formalin- DE LAUBENFELS (1936a:(1936a: 152),152), whowho claimedclaimed thatthat seawater and preserved inin 8080 %% ethanolethanol afterafter 2424 h.h. Terpios is "characterized by thethe quadrilobatequadrilobate formform It was deposited inin thethe collectioncollection ofof thethe NationalNational of the heads of spicules thatthat otherwiseotherwise wouldwould bebe re­re- Museum of Natural History, SmithsonianSmithsonian InstitutionInstitution garded as tylostyles." Subsequently,Subsequently, DEDE LAUBENFELSLAUBENFELS (USNM). (1950:(1950:103)103) was struck by thethe uniqueunique morphologymorphology ofof The skeletal structure was examinedexamined inin sectionssections Terpios tylostyles. InIn particular, hehe consideredconsidered thethe 100 ~m\im thick that were prepared byby grindinggrinding andand pol­pol- relative size of thethe head distinctdistinct amongamong thethe suberitids,suberitids, ishing sponge tissue samplessamples embeddedembedded withwith epoxyepoxy for it was "nearly double oror quitequite doubledouble thethe diame­diame- resin (as described by ROTZLER,RUTZLER, 1978).1978). SpiculesSpicules werewere ter of the spicule shaft."shaft." HeHe alsoalso observedobserved thatthat "in"in isolated and cleaned by boilingboiling inin concentratedconcentrated young sponges" thethe head isis distinctlydistinctly lobate,lobate, "with"with nitricacid and washing inin demineralizeddemineralized waterwater andand indications that thethe laterallateral growthgrowth ofof thisthis headhead hashas absolute alcohol. Measurements areare basedbased onon 2525 ty­ty- (primitively) arisen by polyactinal branching.branching. ItIt maymay lostyles selected at random.random. ToTo revealreveal internalinternal struc­struc- represent a pentactinal spiculespicule withwith fourfour cladsdads inin oneone ture~ure and enhance thethe axialaxial canal,canal, somesome spiculespicule sam­sam- plane, and a very longlong rhabd."rhabd." HisHis interpretationinterpretation ofof ples were concentrated by centrifugationcentrifugation inin epoxyepoxy Terpios appears toto have been biasedbiased byby hishis earlierearlier resin, ground and polished (Carborundum(Carborundum paperpaper andand examinations of encrusting specimensspecimens withwith distinctlydistinctly aluminum oxide, toto 0.3 ~ri m), andand etchedetched byby exposureexposure lobed heads because thethe ensuingensuing descriptiondescription andand dis­dis- to dilute hydrofluoric acidacid (6.5(6.5 %% inin distilleddistilled water)water) cussion of "T. fugax" does notnot mentionmention thesethese charac­charac- for 15 sec. Scanning electronelectron micrographsmicrographs (SEM)(SEM) teristics at all. De Laubenfels was,was, inin fact,fact, describingdescribing were made of spicules andand etchedetched sectionssections usingusing aa T. aurantiaca DUCHASSAING andand Michelotti,Michelotti, notnot thethe Cambridge Stereoscan 100100 microscopemicroscope atat 1,000­1,000- massive growth form or stagestage ofof T.T. fugax,fugax, asas hehe pre­pre- 3,000 xxmagnification.magnification. sumed. For transmission electron microscopymicroscopy (TEM),(TEM), It is not uncommon forfor thethe tylostylestylostyles ofof crustosecrustose material was fixed inin 3.5% glutaraldehydeglutaraldehyde inin 0.10.1 MM sponges to have conspicuously lobedlobed heads.heads. ThisThis fea­fea- phosphate buffer with thethe additionaddition 0.450.45 MM sucrosesucrose ture is seldom mentioned inin thethe literatureliterature becausebecause itit (90 min at 29"29° C), postfixed inin 11 %% osmicosmic acidacid inin thethe is usually seen inin small,small, fragmentary,fragmentary, oror isolatedisolated sam­sam- same buffer mixture (60(60 min atat 4°4" C).C). SectionsSections werewere ples. One exception isis SCHMIDT'SSCHMIDT'S descriptiondescription andand il­il- stained in saturated (5(5 %)%) alcoholicalcoholic uranyluranyl acetateacetate lustration (1870:47; pI.pi. 5,5, fig.fig. 5)5) ofof anan unusualunusual spongesponge with 0.25 % leadlead citrate andand viewedviewed andand photo­photo- crust from Florida, which hehe namednamed SuberitesSuberites lobi­lobi- graphed through a leolJeol 12001200 EXEX electronelectron microscopemicroscope ceps. A specimen with similarsimilar spiculesspicules fromfrom thethe GulfGulf (2,000-12,000 x primary magnification). LightLight mi­mi- of Mexico (TOPSENT, 1920:30)1920:30) waswas identifiedidentified (but(but notnot croscope observations ofof histologyhistology andand skeletonskeleton described) by SCHMIDT 1880:77,1880:77, butbut thisthis speciesspecies hashas structure were made on thethe samesame materialmaterial sectionedsectioned 11 not been found or discussed sincesince thesethese earlyearly reportsreports urn~m thick, or ground and polished toto aa thicknessthickness ofof 5050 and remains obscure; DE LAUBENFELSLAUBENFELS (1950:107)(1950:107) urn,~m, both stained by methylene blue.blue. dropped it in synonymy with T.T. fugax.fugax. The question of validity ofof thethe genusgenus TerpiosTerpios waswas reopened recently inin aa discussion ofof stronglystrongly compe­compe- RESULTS titive Pacific reef speciesspecies ofof TerpiosTerpios withwith distinctlydistinctly lobed tylostyle heads (ROTZLER(RUTZLER andand MUZIK,MUZIK, 1993).1993). 1. Superspecific Characterizations The question could not be addressedaddressed withoutwithout revie­revie- wing T. fugax, thethe genotype, andand thethe statusstatus ofof Suber­Suber- The following diagnoses were compiledcompiled fromfrom vari­vari- ites lobiceps and other closelyclosely relatedrelated speciesspecies withwith un­un- ous sources, primarily TOPSENT (1900),(1900), DEDE LAUBEN­LAUBEN- usual tylostyle heads, includingincluding thethe twotwo newnew onesones FELS (1936a), and LEVI (1973),(1973), andand supplementedsupplemented byby from the Caribbean described inin thisthis report.report. our own observations. CommentsComments onon andand descrip­descrip- tions of examples forfor different generagenera areare basedbased pri­pri- marily on tropical western AtlanticAtlantic
Recommended publications
  • National Monitoring Program for Biodiversity and Non-Indigenous Species in Egypt
    UNITED NATIONS ENVIRONMENT PROGRAM MEDITERRANEAN ACTION PLAN REGIONAL ACTIVITY CENTRE FOR SPECIALLY PROTECTED AREAS National monitoring program for biodiversity and non-indigenous species in Egypt PROF. MOUSTAFA M. FOUDA April 2017 1 Study required and financed by: Regional Activity Centre for Specially Protected Areas Boulevard du Leader Yasser Arafat BP 337 1080 Tunis Cedex – Tunisie Responsible of the study: Mehdi Aissi, EcApMEDII Programme officer In charge of the study: Prof. Moustafa M. Fouda Mr. Mohamed Said Abdelwarith Mr. Mahmoud Fawzy Kamel Ministry of Environment, Egyptian Environmental Affairs Agency (EEAA) With the participation of: Name, qualification and original institution of all the participants in the study (field mission or participation of national institutions) 2 TABLE OF CONTENTS page Acknowledgements 4 Preamble 5 Chapter 1: Introduction 9 Chapter 2: Institutional and regulatory aspects 40 Chapter 3: Scientific Aspects 49 Chapter 4: Development of monitoring program 59 Chapter 5: Existing Monitoring Program in Egypt 91 1. Monitoring program for habitat mapping 103 2. Marine MAMMALS monitoring program 109 3. Marine Turtles Monitoring Program 115 4. Monitoring Program for Seabirds 118 5. Non-Indigenous Species Monitoring Program 123 Chapter 6: Implementation / Operational Plan 131 Selected References 133 Annexes 143 3 AKNOWLEGEMENTS We would like to thank RAC/ SPA and EU for providing financial and technical assistances to prepare this monitoring programme. The preparation of this programme was the result of several contacts and interviews with many stakeholders from Government, research institutions, NGOs and fishermen. The author would like to express thanks to all for their support. In addition; we would like to acknowledge all participants who attended the workshop and represented the following institutions: 1.
    [Show full text]
  • TEXT-BOOKS of ANIMAL BIOLOGY a General Zoology of The
    TEXT-BOOKS OF ANIMAL BIOLOGY * Edited by JULIAN S. HUXLEY, F.R.S. A General Zoology of the Invertebrates by G. S. Carter Vertebrate Zoology by G. R. de Beer Comparative Physiology by L. T. Hogben Animal Ecology by Challes Elton Life in Inland Waters by Kathleen Carpenter The Development of Sex in Vertebrates by F. W. Rogers Brambell * Edited by H. MUNRO Fox, F.R.S. Animal Evolution / by G. S. Carter Zoogeography of the Land and Inland Waters by L. F. de Beaufort Parasitism and Symbiosis by M. Caullery PARASITISM AND ~SYMBIOSIS BY MAURICE CAULLERY Translated by Averil M. Lysaght, M.Sc., Ph.D. SIDGWICK AND JACKSON LIMITED LONDON First Published 1952 !.lADE AND PRINTED IN GREAT BRITAIN BY WILLIAM CLOWES AND SONS, LlMITED, LONDON AND BECCLES CONTENTS LIST OF ILLUSTRATIONS vii PREFACE TO THE ENGLISH EDITION xi CHAPTER I Commensalism Introduction-commensalism in marine animals-fishes and sea anemones-associations on coral reefs-widespread nature of these relationships-hermit crabs and their associates CHAPTER II Commensalism in Terrestrial Animals Commensals of ants and termites-morphological modifications in symphiles-ants.and slavery-myrmecophilous plants . 16 CHAPTER III From Commensalism to Inquilinism and Parasitism Inquilinism-epizoites-intermittent parasites-general nature of modifications produced by parasitism 30 CHAPTER IV Adaptations to Parasitism in Annelids and Molluscs Polychates-molluscs; lamellibranchs; gastropods 40 CHAPTER V Adaptation to Parasitism in the Crustacea Isopoda-families of Epicarida-Rhizocephala-Ascothoracica
    [Show full text]
  • Taxonomy and Diversity of the Sponge Fauna from Walters Shoal, a Shallow Seamount in the Western Indian Ocean Region
    Taxonomy and diversity of the sponge fauna from Walters Shoal, a shallow seamount in the Western Indian Ocean region By Robyn Pauline Payne A thesis submitted in partial fulfilment of the requirements for the degree of Magister Scientiae in the Department of Biodiversity and Conservation Biology, University of the Western Cape. Supervisors: Dr Toufiek Samaai Prof. Mark J. Gibbons Dr Wayne K. Florence The financial assistance of the National Research Foundation (NRF) towards this research is hereby acknowledged. Opinions expressed and conclusions arrived at, are those of the author and are not necessarily to be attributed to the NRF. December 2015 Taxonomy and diversity of the sponge fauna from Walters Shoal, a shallow seamount in the Western Indian Ocean region Robyn Pauline Payne Keywords Indian Ocean Seamount Walters Shoal Sponges Taxonomy Systematics Diversity Biogeography ii Abstract Taxonomy and diversity of the sponge fauna from Walters Shoal, a shallow seamount in the Western Indian Ocean region R. P. Payne MSc Thesis, Department of Biodiversity and Conservation Biology, University of the Western Cape. Seamounts are poorly understood ubiquitous undersea features, with less than 4% sampled for scientific purposes globally. Consequently, the fauna associated with seamounts in the Indian Ocean remains largely unknown, with less than 300 species recorded. One such feature within this region is Walters Shoal, a shallow seamount located on the South Madagascar Ridge, which is situated approximately 400 nautical miles south of Madagascar and 600 nautical miles east of South Africa. Even though it penetrates the euphotic zone (summit is 15 m below the sea surface) and is protected by the Southern Indian Ocean Deep- Sea Fishers Association, there is a paucity of biodiversity and oceanographic data.
    [Show full text]
  • A Novel Dispersal Mechanism of a Coral-Threatening Sponge, Terpios Hoshinota (Suberitidae, Porifera)
    A Novel Dispersal Mechanism of a Coral-Threatening Sponge, Terpios hoshinota (Suberitidae, Porifera) Keryea Soong1,*, Sun-Lin Yang1, and Chaolun Allen Chen2 1Institute of Marine Biology and Asia-Pacific Ocean Research Center, National Sun Yat-sen University, Kaohsiung 804, Taiwan 2Biodiversity Research Center, Academia Sinica, Taipei 115, and Institute of Oceanography, National Taiwan University, Taipei 106, Taiwan (Accepted April 10, 2009) Terpios hoshinota, a blackish encrusting cyanobacteriosponge, is known to overgrow and kill a wide range of stony coral hosts, mostly on Pacific reefs (Bryan 1973, Plucer-Rosario 1987, Rützler and Muzik 1993). An outbreak of the sponge occurred in 2008 at Green I. (22°39'N, 121°29'E), off the southeastern coast of Taiwan, where up to 30% of coral colonies were infected on certain reefs within a couple of years of its first discovery (Liao et al. 2007). In a test of methods to stop the sponge from expanding, we used dark plastic sheets (10 x 10 cm), with transparent ones as controls, to cover the advancing sponge fronts without touching the substrate corals. The idea was to block the sunlight needed by the symbiotic cyanobacteria for growth. The shading caused the coral hosts to bleach and most of the sponges to stop advancing. But, in some cases within 2 wk, the sponges had extended thin tissue threads which crossed the shaded and presumably uninhabitable area under the dark plates. Once reaching light on the other side of the dark plate, the sponge thread quickly expanded in area and resumed normal growth (Fig. 1A). The capability to cross unsuitable habitats with pioneering tissue obviously enables the sponge to overgrow new coral surfaces and infect separate colonies in the neighborhood.
    [Show full text]
  • Appendix: Some Important Early Collections of West Indian Type Specimens, with Historical Notes
    Appendix: Some important early collections of West Indian type specimens, with historical notes Duchassaing & Michelotti, 1864 between 1841 and 1864, we gain additional information concerning the sponge memoir, starting with the letter dated 8 May 1855. Jacob Gysbert Samuel van Breda A biography of Placide Duchassaing de Fonbressin was (1788-1867) was professor of botany in Franeker (Hol­ published by his friend Sagot (1873). Although an aristo­ land), of botany and zoology in Gent (Belgium), and crat by birth, as we learn from Michelotti's last extant then of zoology and geology in Leyden. Later he went to letter to van Breda, Duchassaing did not add de Fon­ Haarlem, where he was secretary of the Hollandsche bressin to his name until 1864. Duchassaing was born Maatschappij der Wetenschappen, curator of its cabinet around 1819 on Guadeloupe, in a French-Creole family of natural history, and director of Teyler's Museum of of planters. He was sent to school in Paris, first to the minerals, fossils and physical instruments. Van Breda Lycee Louis-le-Grand, then to University. He finished traveled extensively in Europe collecting fossils, especial­ his studies in 1844 with a doctorate in medicine and two ly in Italy. Michelotti exchanged collections of fossils additional theses in geology and zoology. He then settled with him over a long period of time, and was received as on Guadeloupe as physician. Because of social unrest foreign member of the Hollandsche Maatschappij der after the freeing of native labor, he left Guadeloupe W etenschappen in 1842. The two chief papers of Miche­ around 1848, and visited several islands of the Antilles lotti on fossils were published by the Hollandsche Maat­ (notably Nevis, Sint Eustatius, St.
    [Show full text]
  • Examples of Sea Sponges
    Examples Of Sea Sponges Startling Amadeus burlesques her snobbishness so fully that Vaughan structured very cognisably. Freddy is ectypal and stenciling unsocially while epithelial Zippy forces and inflict. Monopolistic Porter sailplanes her honeymooners so incorruptibly that Sutton recirculates very thereon. True only on water leaves, sea of these are animals Yellow like Sponge Oceana. Deeper dives into different aspects of these glassy skeletons are ongoing according to. Sponges theoutershores. Cell types epidermal cells form outer covering amoeboid cells wander around make spicules. Check how These Beautiful Pictures of Different Types of. To be optimal for bathing, increasing with examples of brooding forms tan ct et al ratios derived from other microscopic plants from synthetic sponges belong to the university. What is those natural marine sponge? Different types of sponges come under different price points and loss different uses in. Global Diversity of Sponges Porifera NCBI NIH. Sponges EnchantedLearningcom. They publish the outer shape of rubber sponge 1 Some examples of sponges are Sea SpongeTube SpongeVase Sponge or Sponge Painted. Learn facts about the Porifera or Sea Sponges with our this Easy mountain for Kids. What claim a course Sponge Acme Sponge Company. BG Silicon isotopes of this sea sponges new insights into. Sponges come across an incredible summary of colors and an amazing array of shapes. 5 Fascinating Types of what Sponge Leisure Pro. Sea sponges often a tube-like bodies with his tiny pores. Sponges The World's Simplest Multi-Cellular Creatures. Sponges are food of various nudbranchs sea stars and fish. Examples of sponges Answers Answerscom. Sponges info and games Sheppard Software.
    [Show full text]
  • A Soft Spot for Chemistry–Current Taxonomic and Evolutionary Implications of Sponge Secondary Metabolite Distribution
    marine drugs Review A Soft Spot for Chemistry–Current Taxonomic and Evolutionary Implications of Sponge Secondary Metabolite Distribution Adrian Galitz 1 , Yoichi Nakao 2 , Peter J. Schupp 3,4 , Gert Wörheide 1,5,6 and Dirk Erpenbeck 1,5,* 1 Department of Earth and Environmental Sciences, Palaeontology & Geobiology, Ludwig-Maximilians-Universität München, 80333 Munich, Germany; [email protected] (A.G.); [email protected] (G.W.) 2 Graduate School of Advanced Science and Engineering, Waseda University, Shinjuku-ku, Tokyo 169-8555, Japan; [email protected] 3 Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl-von-Ossietzky University Oldenburg, 26111 Wilhelmshaven, Germany; [email protected] 4 Helmholtz Institute for Functional Marine Biodiversity, University of Oldenburg (HIFMB), 26129 Oldenburg, Germany 5 GeoBio-Center, Ludwig-Maximilians-Universität München, 80333 Munich, Germany 6 SNSB-Bavarian State Collection of Palaeontology and Geology, 80333 Munich, Germany * Correspondence: [email protected] Abstract: Marine sponges are the most prolific marine sources for discovery of novel bioactive compounds. Sponge secondary metabolites are sought-after for their potential in pharmaceutical applications, and in the past, they were also used as taxonomic markers alongside the difficult and homoplasy-prone sponge morphology for species delineation (chemotaxonomy). The understanding Citation: Galitz, A.; Nakao, Y.; of phylogenetic distribution and distinctiveness of metabolites to sponge lineages is pivotal to reveal Schupp, P.J.; Wörheide, G.; pathways and evolution of compound production in sponges. This benefits the discovery rate and Erpenbeck, D. A Soft Spot for yield of bioprospecting for novel marine natural products by identifying lineages with high potential Chemistry–Current Taxonomic and Evolutionary Implications of Sponge of being new sources of valuable sponge compounds.
    [Show full text]
  • Proposal for a Revised Classification of the Demospongiae (Porifera) Christine Morrow1 and Paco Cárdenas2,3*
    Morrow and Cárdenas Frontiers in Zoology (2015) 12:7 DOI 10.1186/s12983-015-0099-8 DEBATE Open Access Proposal for a revised classification of the Demospongiae (Porifera) Christine Morrow1 and Paco Cárdenas2,3* Abstract Background: Demospongiae is the largest sponge class including 81% of all living sponges with nearly 7,000 species worldwide. Systema Porifera (2002) was the result of a large international collaboration to update the Demospongiae higher taxa classification, essentially based on morphological data. Since then, an increasing number of molecular phylogenetic studies have considerably shaken this taxonomic framework, with numerous polyphyletic groups revealed or confirmed and new clades discovered. And yet, despite a few taxonomical changes, the overall framework of the Systema Porifera classification still stands and is used as it is by the scientific community. This has led to a widening phylogeny/classification gap which creates biases and inconsistencies for the many end-users of this classification and ultimately impedes our understanding of today’s marine ecosystems and evolutionary processes. In an attempt to bridge this phylogeny/classification gap, we propose to officially revise the higher taxa Demospongiae classification. Discussion: We propose a revision of the Demospongiae higher taxa classification, essentially based on molecular data of the last ten years. We recommend the use of three subclasses: Verongimorpha, Keratosa and Heteroscleromorpha. We retain seven (Agelasida, Chondrosiida, Dendroceratida, Dictyoceratida, Haplosclerida, Poecilosclerida, Verongiida) of the 13 orders from Systema Porifera. We recommend the abandonment of five order names (Hadromerida, Halichondrida, Halisarcida, lithistids, Verticillitida) and resurrect or upgrade six order names (Axinellida, Merliida, Spongillida, Sphaerocladina, Suberitida, Tetractinellida). Finally, we create seven new orders (Bubarida, Desmacellida, Polymastiida, Scopalinida, Clionaida, Tethyida, Trachycladida).
    [Show full text]
  • BIO 313 ANIMAL ECOLOGY Corrected
    NATIONAL OPEN UNIVERSITY OF NIGERIA SCHOOL OF SCIENCE AND TECHNOLOGY COURSE CODE: BIO 314 COURSE TITLE: ANIMAL ECOLOGY 1 BIO 314: ANIMAL ECOLOGY Team Writers: Dr O.A. Olajuyigbe Department of Biology Adeyemi Colledge of Education, P.M.B. 520, Ondo, Ondo State Nigeria. Miss F.C. Olakolu Nigerian Institute for Oceanography and Marine Research, No 3 Wilmot Point Road, Bar-beach Bus-stop, Victoria Island, Lagos, Nigeria. Mrs H.O. Omogoriola Nigerian Institute for Oceanography and Marine Research, No 3 Wilmot Point Road, Bar-beach Bus-stop, Victoria Island, Lagos, Nigeria. EDITOR: Mrs Ajetomobi School of Agricultural Sciences Lagos State Polytechnic Ikorodu, Lagos 2 BIO 313 COURSE GUIDE Introduction Animal Ecology (313) is a first semester course. It is a two credit unit elective course which all students offering Bachelor of Science (BSc) in Biology can take. Animal ecology is an important area of study for scientists. It is the study of animals and how they related to each other as well as their environment. It can also be defined as the scientific study of interactions that determine the distribution and abundance of organisms. Since this is a course in animal ecology, we will focus on animals, which we will define fairly generally as organisms that can move around during some stages of their life and that must feed on other organisms or their products. There are various forms of animal ecology. This includes: • Behavioral ecology, the study of the behavior of the animals with relation to their environment and others • Population ecology, the study of the effects on the population of these animals • Marine ecology is the scientific study of marine-life habitat, populations, and interactions among organisms and the surrounding environment including their abiotic (non-living physical and chemical factors that affect the ability of organisms to survive and reproduce) and biotic factors (living things or the materials that directly or indirectly affect an organism in its environment).
    [Show full text]
  • Disappearance and Return of an Outbreak of the Coral-Killing
    Zoological Studies 56: 7 (2017) doi:10.6620/ZS.2017.56-07 Disappearance and Return of an Outbreak of the Coral-killing Cyanobacteriosponge Terpios hoshinota in Southern Japan Masashi Yomogida1, Masaru Mizuyama2, Toshiki Kubomura3, and James Davis Reimer1,2,3,4,* 1Molecular Invertebrate Systematics and Ecology Laboratory, Department of Biology, Chemistry and Marine Sciences, Faculty of Science, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan. E-mail: [email protected] 2Molecular Invertebrate Systematics and Ecology Laboratory, Graduate School of Science and Engineering, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan. E-mail: [email protected] 3Molecular Invertebrate Systematics and Ecology Laboratory, Graduate School of Science and Engineering, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan. E-mail: [email protected] 4Tropical Biosphere Research Center, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan (Received 6 October 2016; Accepted 21 March 2017; Published 19 April 2017; Communicated by Yoko Nozawa) Masashi Yomogida, Masaru Mizuyama, Toshiki Kubomura, and James Davis Reimer (2017) Terpios hoshinota is cyanobacteriosponge that can cause serious damage to coral reef ecosystems by undergoing rapid breakouts in which it smothers and encrusts hard substrates, killing living sessile benthic organisms and reducing biodiversity of the affected area. The reasons for these outbreaks are still unclear, as are long-term prognoses of affected reefs. Some reports have suggested outbreaks may not be permanent, but very little long-term monitoring information exists. In this study, we report on a T. hoshinota outbreak (~24% coverage) at Yakomo, Okinoerabu-jima Island, Kagoshima, Japan between 2010 to 2014.
    [Show full text]
  • The Unique Skeleton of Siliceous Sponges (Porifera; Hexactinellida and Demospongiae) That Evolved first from the Urmetazoa During the Proterozoic: a Review
    Biogeosciences, 4, 219–232, 2007 www.biogeosciences.net/4/219/2007/ Biogeosciences © Author(s) 2007. This work is licensed under a Creative Commons License. The unique skeleton of siliceous sponges (Porifera; Hexactinellida and Demospongiae) that evolved first from the Urmetazoa during the Proterozoic: a review W. E. G. Muller¨ 1, Jinhe Li2, H. C. Schroder¨ 1, Li Qiao3, and Xiaohong Wang4 1Institut fur¨ Physiologische Chemie, Abteilung Angewandte Molekularbiologie, Duesbergweg 6, 55099 Mainz, Germany 2Institute of Oceanology, Chinese Academy of Sciences, 7 Nanhai Road, 266071 Qingdao, P. R. China 3Department of Materials Science and Technology, Tsinghua University, 100084 Beijing, P. R. China 4National Research Center for Geoanalysis, 26 Baiwanzhuang Dajie, 100037 Beijing, P. R. China Received: 8 January 2007 – Published in Biogeosciences Discuss.: 6 February 2007 Revised: 10 April 2007 – Accepted: 20 April 2007 – Published: 3 May 2007 Abstract. Sponges (phylum Porifera) had been considered an axial filament which harbors the silicatein. After intracel- as an enigmatic phylum, prior to the analysis of their genetic lular formation of the first lamella around the channel and repertoire/tool kit. Already with the isolation of the first ad- the subsequent extracellular apposition of further lamellae hesion molecule, galectin, it became clear that the sequences the spicules are completed in a net formed of collagen fibers. of sponge cell surface receptors and of molecules forming the The data summarized here substantiate that with the find- intracellular signal transduction pathways triggered by them, ing of silicatein a new aera in the field of bio/inorganic chem- share high similarity with those identified in other metazoan istry started.
    [Show full text]
  • Suberitidae (Demospongiae, Hadromerida) From
    Beaufortia INSTITUTE OF TAXONOMIC ZOOLOGY (ZOOLOGICAL MUSEUM) UNIVERSITY OF AMSTERDAM Vol. 43 no. 11 December 31, 1993 Suberitidae (Demospongiae, Hadromerida) from the North Aegean Sea EleniVoultsiadou-Koukoura.*& Rob W. M. van Soest** *Department University ofThessaloniki, 54006 Thessaloniki, Greece **Institute of Taxonomic (Zoological Museum), University ofAmsterdam, P.O.Box 94766, 1090 GTAmsterdam, TheNetherlands Keywords: Sponges, Hadromerida, Suberitidae, North Aegean Sea Abstract Sampling in the North Aegean Sea yielded nine species of the family Suberitidae, four of which, Pseudosuberites sulphureus, P. Suberiles for the fauna ofthe Eastern and three hyalinus, ficus and S. syringella, are new Mediterranean, more, S. carnosus, S. and S. records for the fauna of the Sea. For each of the nine the domuncula, massa, are new Aegean species comments on systematics, as well as geographical and ecological informationis given. A redescription is given of the littleknown species Suberites massa Nardo. A review ofthe distributionof all Mediterranean Suberitidae is also presented, in which it is con- in materialhave been from the Eastern cluded that a further three species not represented our reported Mediterranean, and P. the viz. Laxosuberites ectyoninus, Prosuberites longispina, epiphytum. Six suberitids reported from other parts of Mediterra- nean so far have not been found in the Eastern Mediterranean. INTRODUCTION siadou-Koukoura, et al. 1991; Voultsiadou- Koukoura & Van Soest 1991a,b; Voultsiadou- of Eastern Mediterranean is Koukoura & the results of the Knowledge sponges Koukouras, 1993), that of other of the Med- have been and are poor compared to parts sponge collecting being re- iterranean Van 1994: Recent several science and (cf. Soest, Fig. 2). ported; species new to appar- collecting activities in the North Aegean Sea ently endemic to the Eastern Mediterranean been of have been described.
    [Show full text]