Article Sencer

Total Page:16

File Type:pdf, Size:1020Kb

Article Sencer Butll. Inst. Cat. Hist. Nat., 47 (Sec. Zool., 4): 5-59. 1981 ESTUDI FAUNISTIC DEL LITORAL DE BLANES (GIRONA), II. SISTEMATICA D'ESPONGES Rebut: desembre 1980 * Maria-Antonia Bibiloni ABSTRACT Faunistic study of the Blanes ( Girona , Spain ) littoral , II. Porifera systematics. been The benthic communities of a little area in the Blanes littoral (Girona, Spain) have 12 m studied for two years. They belong to the upper infralittoral level, between 3 and sam- deep, and have been studied from 40 inventories obtained from punctual underwater as- ples and from a general survey of the macroflora and macrofauna. Three bionomic pects with minor differences have been observed in this area: A, well lighted and surf- beaten zones with a population of photophilous species; B, poor lighted and surf-beaten zones, with more sciaphilous forms, and C, poor lighted and less disturbed zones, of coralligenous character. This paper deals with the study of the Porifera species found in the abovemen- tioned survey, of which a systematic list is presented. Thirty-nine species of sponges have been obtained; 7 of them are recorded for the first time in the Catalan coast, and of these 5 are new citations for the Iberian Peninsula littoral. The in vivo and spicular descriptions of each species, data on their habitat, geographic distribution, substrate, depth and bionomic facies are given. Some general ecological remarks are also made from the abundance distribution of each species in the bionomic zones of the area. INTRODUCCIO Aquests estudis van portar a terme l'e- laboracio d'una monografia (BIBILON, Durant dos anys s'han estudiat, amb 1980) d'on s'han extret una serie de tre- I'ajut do l'escafrandre autonom, les co- balls sistematics, ecologics i bionomics munitats bentoniques d'una petita zona (BIBILONI, 1981; BIBILONI & CORNET, 1981a, del litoral de Blanes (Girona) correspo- 1981b; BIBILONI et al., 1981). Un d'aquests nent al pis infralitoral superior, entre 3 treballs es el present article, encaminat a i 12 m, a partir d'inventaris procedents l'estudi de la sistematics dels porffers de de mostres puntuals i d'una descripcio la zona. general de la macroflora i de la macro- La situacio geografica de Blanes es in- fauna de la zona. teressant perque es troba en el limit de * Departament d'Ecologia. Facultat de Biologia. Univershat de Barcelona. Gran Via de les Corts Catalanes, 585. Barcelona, 7. 5 dos tipus de costa molt diferents (fig. 1), costa uns 60 m. S'ha considerat cl limit el Maresme, que es sorrenca, i la Costa de la zona als 5 m de profunditat. Brava estricta, essencialment rocosa. Si De les zones intermedies s'ha fet un a aixo s'afegcix 1'existencia d'un entrant estudi cartografic i bionomic mitjancant del talus continental que fa que s'arribi inventaris visuals i fotografics. a una profunditat de 200 m a uns 5,5 km S'han diferenciat a la zona de mostrat- de la costa, es veu que es facil de trobar, ge tres aspectes bionomics lleugerament en una superffcie relativament petita, una diferents : A, zones illuminades i batudes gran diversitat de fops, anomenats en amb abundancia d'especies fotofiles. B, part per Ros (1975): fons de dintre del zones menys illuminades i batudes amb port; roques litorals de 0 a 25 m de pro- caracter mes esci.afil. C, zones de poca funditat; fons sorrencs fins a 40 m amb il•luminacio amb caracter coralligen (vegeu prats de Posidonia oceanica, al voltant BIBILONI et al., 1981). dcls 20 m; fons corraflfgens amb detritus S'ha efectuat un total de 40 inventaris i sorra, molt rics en fauna invertebrada; repartits d'aquesta manera: 13 en la zo- fons detrItics costaners i detrftics amb na 1, 19 en la zona 2 i 8 en la zona 3, els sediments importants de sorra i fang; fons quals s'han numerat cronologicament; les de fangs terrfgens, rics en poliquets i cc- mostres s 'han agrupat segons la zona bio- lenteris; i fangs batials, a mes de 300 m nomica a la qual pertanyen ( vegeu taula 1). de profunditat, pobres en fauna inverte- En aquest treball s'estudia el tipus Pori- brada en general. fera; a mes d 'una llista sistematica de les Dins del segon tipus de fons, es a dir, especics trobades , es dona una descrip- en les roques litorals de 0 a 25 m de pro- cio detallada de cada una, taut del seu funditat amb abundancia d'algues foto- aspecte extern com del seu esquelet, com- files i corafligen incipient a partir dels pletant-ho amb la seva distribucio i el seu 20 m, situa ]'area objecte d'estudi. Aques- habitat. ta to uns 13.500 m2, es situada entre la Igualment s'exposa per a cada exem- punta de Santa Anna i la cala de Sant plar informacio referent a la data, subs- Francesc i es delimitada al nord per blocs trat, profunditat i facies bionomica en submergits d'aquesta punta i al sud per que es troba. grans blocs rocosos que surten a la su- perffcie. Per terra s'hi arriba per una pe- tita platja de recent construccio, orienta- ANTECEDENTS HISTORICS da al N-NE i, per tant, rep la influencia dels vents del N tramuntana), NE (gre- La importancia dels porffers dintre de gal) i E (llevant), qucdant bastant prote- les poblacions bentoniques de substrat dur gida del SE (xaloc) i S (migjorn) per la no s'ha comencat a apreciar fins fa pocs platja artificial que uneix l'espigo portua- anys, malgrat que des de fa temps s'hagi ri amb la punta de Santa Anna. estudiat aquest grup a la Mediterrania En aquesta zona s'han elegit tres esta- (Schmidt, Lendenfeld, Ferrer Hernandez, cions fixes per a fer-hi mostratges perio- Topscnt). La rao principal es deguda als dicament: metodes de recolleccio, que, antigament, - Zona 1; petit illot que sobrcsurt del eren nomes indirectes (dragues) i no ofe- nivell de l'aigua uns 70 cm; queda sepa- rien cap informacio de ]'habitat del grup. rat de la costa uns 70 m; s'hi han obtin- L'us de 1'escafandre autonom ha permes gut mostres de diferents orientacions. La millorar les tecniques de recol•leccio del maxima profunditat a que s'arriba es de bentos i afrontar estudis de bionomia mes 7 m. complerts. - Zona 2; formada per una paret ver- L'cstudi de les esponges a la Peninsula tical que des del nivell de l'aigua arriba Iberica es remunta a principi de segle, fins a 12 m, orientada a 1'est, i una altra amb ORUETA (1901), que descrivf algunes a la mateixa profunditat i que no arriba esponges del Cantabric. a la superffcie, orientada a l'oest. Totes FERRER HERNANDEZ (1912, 1914a, 1914b, dues son a uns 12 m de la costa; s'han 1916, 1917, 1918, 1921, 1922) estudia la cos- agafat tambe mostres dels voltants. ta cantabrica i altres punts del litoral es- - Zona 3; correspon a la part submer- panyol. Els metodes de recolleccio son gida de la punta de Santa Anna, seguint indirectes i no aporten cap informacio so- una direccio NW-SE, i es separada de la bre I'habitat de les espccies recollectades, 6 N 250 500 m FIG. 1. Situacio geografica de Blanes i de la zona d'estudi. Geographical situation of Blanes and estudy's zone. 7 . - - - - - - - - .11 - - - - . - - . `^ `^ ,^ ^.ro 0 y a ti .^ c v ^n a v E ^. ^ .a Ev o a. a a ^ 'L b ^ > ^ b b .^ (d Q ^ i' . U y 7 , * I I * I I - - - - - - - - - - - - - 'C ^ ^ 7 C G _O ^ .^ A •^ ro C] ^d ^ .? C. C R M ^ O A c u L^ C J vI v W 1--I v a 0 4 ti C t [. 7 E o Z G^ Q U L q R C u L^ sU^ w A U_ A 4 c. c e A m m m 0 J c c o o -^ c a c a s u t ^ a S !! c c E r E v^ R C ^"^ a e n u S 0 <^ .^ encara que la tasca faunistica i sistema- Les esponges es mantenien amb aigua de tica rs important. mar durant 24 hores, per tal que s'obris- RUiu i (1971) estudia les esponges de sin els osculs i el sistema aquifer, anotant Blanes, do fons sorrencs principalment, al mateix temps tots aquells caracters que Inntament amb altres grups d'inventcbrats es poguessin modificar despres de la fixa- i ttinicats. Encara quc represcnti una con- cio (color, consistencia, ostiols i osculs). Ii ibucio interessant al coneixement de Despres de scr fixades amb formol al 4 °/o Ics comunitats naturals do les nostres cos- es determinaven sistematicament segons tcs, no toca els substrats durs. els metodes classics. Dins del PROGRAyIA in: BENTOS (1972-74), Oi.nvri i.v (1977) analitza la distribucio de Ics esponges tie foes rocosos del litoral RELACIO D'ESPECIES catakt, ja amb inetodes directes (escafan- dre autonom), essent aquest el primer tre- En la llista que scgueix s'ordenen taxo- ball realitzat a les cosies catalanes amb nomicament les especies d'esponges deter- aquest metode. Mes tard (OLivELLA, 1980) minades, assenyalant-se si es tracta d'una s'ocupa de les esponges de les illes Medes nova citacio per la costa catalana (+) o (Girona). si l'especie es nova per a la fauna iberi- BENITO (1976) estudia les esponges de la ca (++). ria de Vigo. Despres RODRIGUEZ & LOREN- Aquesta Ilista s'ha fet seguint 1'ordre zo (1978) descriuen les csponges interma- sistematic donat per TUZET (1973) per les reals d'aquesta localitat.
Recommended publications
  • 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]
  • Transcriptome Sequencing, Characterization and Overview of the Gene Expression Along Three Life Cycle Stages
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital.CSIC Molecular Ecology Resources (2013) doi: 10.1111/1755-0998.12085 A NGS approach to the encrusting Mediterranean sponge Crella elegans (Porifera, Demospongiae, Poecilosclerida): transcriptome sequencing, characterization and overview of the gene expression along three life cycle stages A. R. PEREZ-PORRO,*† D. NAVARRO-GOMEZ,† M. J. URIZ* and G. GIRIBET† *Center for Advanced Studies of Blanes (CEAB-CSIC), c/Acces a la Cala St. Francesc 14, Girona, Blanes 17300, Spain, †Museum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA Abstract Sponges can be dominant organisms in many marine and freshwater habitats where they play essential ecological roles. They also represent a key group to address important questions in early metazoan evolution. Recent approaches for improving knowledge on sponge biological and ecological functions as well as on animal evolution have focused on the genetic toolkits involved in ecological responses to environmental changes (biotic and abiotic), development and reproduction. These approaches are possible thanks to newly available, massive sequencing tech- nologies–such as the Illumina platform, which facilitate genome and transcriptome sequencing in a cost-effective manner. Here we present the first NGS (next-generation sequencing) approach to understanding the life cycle of an encrusting marine sponge. For this we sequenced libraries of three different life cycle stages of the Mediterranean sponge Crella elegans and generated de novo transcriptome assemblies. Three assemblies were based on sponge tissue of a particular life cycle stage, including non-reproductive tissue, tissue with sperm cysts and tissue with larvae.
    [Show full text]
  • Ereskovsky Et 2018 Bulgarie.Pd
    Sponge community of the western Black Sea shallow water caves: diversity and spatial distribution Alexander Ereskovsky, Oleg Kovtun, Konstantin Pronin, Apostol Apostolov, Dirk Erpenbeck, Viatcheslav Ivanenko To cite this version: Alexander Ereskovsky, Oleg Kovtun, Konstantin Pronin, Apostol Apostolov, Dirk Erpenbeck, et al.. Sponge community of the western Black Sea shallow water caves: diversity and spatial distribution. PeerJ, PeerJ, 2018, 6, pp.e4596. 10.7717/peerj.4596. hal-01789010 HAL Id: hal-01789010 https://hal.archives-ouvertes.fr/hal-01789010 Submitted on 14 May 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. Sponge community of the western Black Sea shallow water caves: diversity and spatial distribution Alexander Ereskovsky1,2, Oleg A. Kovtun3, Konstantin K. Pronin4, Apostol Apostolov5, Dirk Erpenbeck6 and Viatcheslav Ivanenko7 1 Institut Méditerranéen de Biodiversité et d'Ecologie Marine et Continentale (IMBE), Aix Marseille University, CNRS, IRD, Avignon Université, Marseille, France 2 Department of Embryology, Faculty of Biology,
    [Show full text]
  • Transcriptome Sequencing, Characterization and Overview of the Gene Expression Along Three Life Cycle Stages
    Molecular Ecology Resources (2013) doi: 10.1111/1755-0998.12085 A NGS approach to the encrusting Mediterranean sponge Crella elegans (Porifera, Demospongiae, Poecilosclerida): transcriptome sequencing, characterization and overview of the gene expression along three life cycle stages A. R. PEREZ-PORRO,*† D. NAVARRO-GOMEZ,† M. J. URIZ* and G. GIRIBET† *Center for Advanced Studies of Blanes (CEAB-CSIC), c/Acces a la Cala St. Francesc 14, Girona, Blanes 17300, Spain, †Museum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA Abstract Sponges can be dominant organisms in many marine and freshwater habitats where they play essential ecological roles. They also represent a key group to address important questions in early metazoan evolution. Recent approaches for improving knowledge on sponge biological and ecological functions as well as on animal evolution have focused on the genetic toolkits involved in ecological responses to environmental changes (biotic and abiotic), development and reproduction. These approaches are possible thanks to newly available, massive sequencing tech- nologies–such as the Illumina platform, which facilitate genome and transcriptome sequencing in a cost-effective manner. Here we present the first NGS (next-generation sequencing) approach to understanding the life cycle of an encrusting marine sponge. For this we sequenced libraries of three different life cycle stages of the Mediterranean sponge Crella elegans and generated de novo transcriptome assemblies. Three assemblies were based on sponge tissue of a particular life cycle stage, including non-reproductive tissue, tissue with sperm cysts and tissue with larvae. The fourth assembly pooled the data from all three stages.
    [Show full text]
  • Molecular Phylogenies Confirm the Presence of Two Cryptic Hemimycale
    Molecular phylogenies confirm the presence of two cryptic Hemimycale species in the Mediterranean and reveal the polyphyly of the genera Crella and Hemimycale (Demospongiae: Poecilosclerida) Maria J. Uriz, Leire Garate and Gemma Agell Department of Marine Ecology, Centre for Advanced Studies of Blanes (CEAB-CSIC), Blanes, Girona, Spain ABSTRACT Background: Sponges are particularly prone to hiding cryptic species as their paradigmatic plasticity often favors species phenotypic convergence as a result of adaptation to similar habitat conditions. Hemimycale is a sponge genus (Family Hymedesmiidae, Order Poecilosclerida) with four formally described species, from which only Hemimycale columella has been recorded in the Atlanto-Mediterranean basin, on shallow to 80 m deep bottoms. Contrasting biological features between shallow and deep individuals of Hemimycale columella suggested larger genetic differences than those expected between sponge populations. To assess whether shallow and deep populations indeed belong to different species, we performed a phylogenetic study of Hemimycale columella across the Mediterranean. We also included other Hemimycale and Crella species from the Red Sea, with the additional aim of clarifying the relationships of the genus Hemimycale. Methods: Hemimycale columella was sampled across the Mediterranean, and Adriatic Seas. Hemimycale arabica and Crella cyathophora were collected from Submitted 19 November 2016 the Red Sea and Pacific. From two to three specimens per species and locality Accepted 4 January 2017 were extracted, amplified for Cytochrome C Oxidase I (COI) (M1–M6 partition), Published 7 March 2017 18S rRNA, and 28S (D3–D5 partition) and sequenced. Sequences were aligned using Corresponding author Clustal W v.1.81. Phylogenetic trees were constructed under neighbor joining (NJ), Maria J.
    [Show full text]
  • Transcriptomic Analysis of Differential Host Gene
    Riesgo et al. BMC Genomics 2014, 15:376 http://www.biomedcentral.com/1471-2164/15/376 RESEARCH ARTICLE Open Access Transcriptomic analysis of differential host gene expression upon uptake of symbionts: a case study with Symbiodinium and the major bioeroding sponge Cliona varians Ana Riesgo1,2†, Kristin Peterson3,4, Crystal Richardson3,5,TylerHeist3,BrianStrehlow3,6, Mark McCauley3,7, Carlos Cotman3, Malcolm Hill3*† and April Hill3*† Abstract Background: We have a limited understanding of genomic interactions that occur among partners for many symbioses. One of the most important symbioses in tropical reef habitats involves Symbiodinium. Most work examining Symbiodinium-host interactions involves cnidarian partners. To fully and broadly understand the conditions that permit Symbiodinium to procure intracellular residency, we must explore hosts from different taxa to help uncover universal cellular and genetic strategies for invading and persisting in host cells. Here, we present data from gene expression analyses involving the bioeroding sponge Cliona varians that harbors Clade G Symbiodinium. Results: Patterns of differential gene expression from distinct symbiont states (“normal”, “reinfected”,and“aposymbiotic”) of the sponge host are presented based on two comparative approaches (transcriptome sequencing and suppressive subtractive hybridization (SSH)). Transcriptomic profiles were different when reinfected tissue was compared to normal and aposymbiotic tissue. We characterized a set of 40 genes drawn from a pool of differentially expressed
    [Show full text]
  • Sponge Ecology in the Molecular Era
    Sponge Ecology in the Molecular Era Maria J. Uriz1 and Xavier Turon Depatment of Marine Ecology Centre d’Estudis Avançats de Blanes (CEAB-CSIC) Crta. Accés Cala St Francesc, 14 17300 Blanes (Girona). Spain 1 [email protected], Corresponding author [email protected] TABLE OF CONTENTS 1. Introduction 2. Where molecular markers alert us about hidden sponge diversity: cryptic speciation and its ecological repercussions 2.1 Role of molecular markers in the discovery of cryptic sponge species. 2.2. Representative case examples 2.3. Conclusions 3. Population genetics and phylogeography 3.1. Choice of variable molecular markers at the intraspecies level 3.2. Genetic differentiation at large and regional geographical scales 3.3. Small-scale genetic structure 3.4. Temporal genetic structure 3.5. Conclusions 4. Contribution of asexual phenomena to population structure: clonality and chimerism in sponges. 4.1. Sponge asexual propagules 4.2. Clonality in sponge populations 1 4.3. Sponge chimerism 4.4. Conclusions 5. Differential expression of functional genes 5.1. Genetic and environmental regulators of sponge biomineralization 5.2. Pollutants, stress, and gene expression 5.3. Symbioses and horizontal gene transfer 5.4. Expression of other sponge genes with ecological implications. 5.5. Conclusions 6. Forthcoming trends in sponge molecular ecology: hopes and prospects 7. Acknowledgements 8. References Abstract Knowledge of the functioning, health state, and capacity for recovery of marine benthic organisms and assemblages has become essential to adequately manage and preserve marine biodiversity. Molecular tools have allowed an entirely new way to tackle old and new questions in conservation biology and ecology, and sponge science is following this lead.
    [Show full text]
  • Cytonuclear Interactions in the Evolution of Animal Mitochondrial Trna Metabolism
    GBE Cytonuclear Interactions in the Evolution of Animal Mitochondrial tRNA Metabolism Walker Pett1,2 and Dennis V. Lavrov1,* 1Department of Ecology, Evolution and Organismal Biology, Iowa State University 2Present address: Laboratoire de Biome´trieetBiologieE´volutive CNRS UMR 5558, Universite´ Lyon 1, Villeurbanne, France *Corresponding author: E-mail: [email protected]. Accepted: June 22, 2015 Data deposition: Raw genomic sequencing data for Corticium candelabrum have been deposited at the NCBI Sequence Read Archive under the accession SRR2021567. The Corticium candelabrum genome assembly and phylogenetic profiling sequence alignments have been placed on FigShare, doi: 10.6084/m9.figshare.1412684. Mitochondrial DNA sequences from Crella elegans and Petrosia ficiformis have been deposited at GenBank under the accessions KR911862 and KR911863, respectively. Abstract The evolution of mitochondrial information processing pathways, including replication, transcription and translation, is characterized by the gradual replacement of mitochondrial-encoded proteins with nuclear-encoded counterparts of diverse evolutionary origins. Although the ancestral enzymes involved in mitochondrial transcription and replication have been replaced early in eukaryotic evolution, mitochondrial translation is still carried out by an apparatus largely inherited from the a-proteobacterial ancestor. However, variation in the complement of mitochondrial-encoded molecules involved in translation, including transfer RNAs (tRNAs), provides evidence for the ongoing evolution of mitochondrial protein synthesis. Here, we investigate the evolution of the mitochondrial translational machinery using recent genomic and transcriptomic data from animals that have experienced the loss of mt-tRNAs, including phyla Cnidaria and Ctenophora, as well as some representatives of all four classes of Porifera. We focus on four sets of mitochondrial enzymes that directly interact with tRNAs: Aminoacyl-tRNA synthetases, glutamyl-tRNA amidotransferase, tRNAIle lysidine synthetase, and RNase P.
    [Show full text]
  • Sponge Community of the Western Black Sea Shallow Water Caves: Diversity and Spatial Distribution
    Sponge community of the western Black Sea shallow water caves: diversity and spatial distribution Alexander Ereskovsky1,2, Oleg A. Kovtun3, Konstantin K. Pronin4, Apostol Apostolov5, Dirk Erpenbeck6 and Viatcheslav Ivanenko7 1 Institut Méditerranéen de Biodiversité et d'Ecologie Marine et Continentale (IMBE), Aix Marseille University, CNRS, IRD, Avignon Université, Marseille, France 2 Department of Embryology, Faculty of Biology, Saint-Petersburg State University, Saint-Petersburg, Russia 3 Hydrobiology and General Ecology Department, Marine Research Station, Odessa National I. I. Mechnikov University, Odessa, Ukraine 4 Physical and Marine Geology Department, Odessa National I. I. Mechnikov University, Odessa, Ukraine 5 Burgas University, Burgas, Bulgaria 6 Department of Earth and Environmental Sciences & GeoBio-Center, Ludwig-Maximilians-Universität München, Munich, Germany 7 Department of Invertebrate Zoology, Biological Faculty, Moscow State University, Moscow, Russia ABSTRACT Marine caves possess unique biocoenotic and ecological characteristics. Sessile benthic species such as sponges associated with cave habitats typically show a marked zonation from the cave entrance towards the end of the cave. We describe three semi-submerged karstic caves of 50 to 83 m length and 936 to 2,291 m3 volume from the poorly explored cavernicolous fauna of North-East Bulgaria. We surveyed sponge diversity and spatial variability. Eight demosponge species were identified based on morphological and molecular data, of which six are known from the adjacent open sea waters of the Black Sea. Two species, Protosuberites denhartogi van Soest & de Kluijver, 2003 and Halichondria bowerbanki Burton, 1930, are reported from the Black Sea for the first time. The spatial sponge distribution inside the caves is in general similar, but shows some differences in species composition and distribution depending on cave relief and Submitted 22 December 2017 hydrodynamics.
    [Show full text]
  • Sterol and Genomic Analyses Validate the Sponge Biomarker Hypothesis
    Sterol and genomic analyses validate the sponge biomarker hypothesis David A. Golda, Jonathan Grabenstattera, Alex de Mendozab, Ana Riesgoc, Iñaki Ruiz-Trillob,d, and Roger E. Summonsa,1 aDepartment of Earth, Atmospheric and Planetary Science, Massachusetts Institute of Technology, Cambridge, MA 02139; bInstitut de Biologia Evolutiva (Consejo Superior de Investigaciones CientÍficas-Universitat Pompeu Fabra), 08003 Barcelona, Spain; cDepartment of Life Sciences, Natural History Museum of London, London SW7 5BD, United Kingdom; and dInstitut Català de Recerca i Estudis Avançats (ICREA), 08010 Barcelona, Spain Edited by Katherine H. Freeman, Pennsylvania State University, University Park, PA, and approved January 21, 2016 (received for review June 26, 2015) Molecular fossils (or biomarkers) are key to unraveling the deep the oldest evidence for animals in the geologic record. Sub- history of eukaryotes, especially in the absence of traditional sequently, this biomarker is commonly used as a calibration point fossils. In this regard, the sterane 24-isopropylcholestane has been when estimating molecular clocks (5–8) and in the interpretation proposed as a molecular fossil for sponges, and could represent of Precambrian fossils and geology (9–11). However, several the oldest evidence for animal life. The sterane is found in rocks recent papers have challenged the sponge affinity of this bio- ∼650–540 million y old, and its sterol precursor (24-isopropylcholes- marker (12, 13), arguing that (i) pelagophyte algae also produce terol, or 24-ipc) is synthesized today by certain sea sponges. How- 24-ipc, meaning they or their ancestors could be responsible for ever, 24-ipc is also produced in trace amounts by distantly related the sterane, and (ii) there is a general lack of information pelagophyte algae, whereas only a few close relatives of sponges about the distribution of C30 sterols within the eukaryotes.
    [Show full text]
  • Demospongiae Incertae Sedis)
    bioRxiv preprint doi: https://doi.org/10.1101/793372; this version posted October 4, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Phylogenetic relationships of heteroscleromorph demosponges and the affinity of the genus Myceliospongia (Demospongiae incertae sedis) Dennis V. Lavrova, Manuel Maldonadob, Thierry Perezc, Christine Morrowd,e aDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University bDepartment of Marine Ecology, Centro de Estudios Avanzados de Blanes (CEAB-CSIC) cInstitut M´editerran´een de la Biodiversit´e et d’Ecologie marine et continentale (IMBE), CNRS, Aix-Marseille Universit´e, IRD, Avignon Universit´e dZoology Department, School of Natural Sciences & Ryan Institute, NUI Galway, University Road, Galway eIreland and Queen’s University Marine Laboratory, 12–13 The Strand, Portaferry, Northern Ireland Abstract Class Demospongiae – the largest in the phylum Porifera (Sponges) – encompasses 7,581 accepted species across the three recognized subclasses: Keratosa, Verongimorpha, and Heteroscleromorpha. The latter subclass con- tains the majority of demosponge species and was previously subdivided into subclasses Heteroscleromorpha sensu stricto and Haploscleromorpha. The current classification of demosponges is the result of nearly three decades of molecular studies that culminated in a formal proposal of a revised taxon- omy (Morrow and Cardenas, 2015). However, because most of the molecular work utilized partial sequences of nuclear rRNA genes, this classification scheme needs to be tested by additional molecular markers. Here we used sequences and gene order data from complete or nearly complete mitochon- drial genomes of 117 demosponges (including 60 new sequences determined for this study and 6 assembled from public sources) and three additional par- tial mt-genomes to test the phylogenetic relationships within demosponges in general and Heteroscleromorpha sensu stricto in particular.
    [Show full text]
  • Updated Checklist of Sponges (Porifera) Along the Coasts of Turkey
    Turkish Journal of Zoology Turk J Zool (2014) 38: http://journals.tubitak.gov.tr/zoology/ © TÜBİTAK Research Article doi:10.3906/zoo-1405-79 Updated checklist of sponges (Porifera) along the coasts of Turkey 1,2 3, Bülent TOPALOĞLU , Alper EVCEN * 1 Department of Marine Biology, Faculty of Fisheries, İstanbul University, İstanbul, Turkey 2 Turkish Marine Research Foundation, İstanbul, Turkey 3 Department of Hydrobiology, Faculty of Fisheries, Ege University, Bornova, İzmir, Turkey Received: 30.05.2014 Accepted: 28.08.2014 Published Online: 00.00.2013 Printed: 00.00.2013 Abstract: This study compiled the data from previous papers emphasizing sponge species on the Turkish coasts. In total, 127 species belonging to 46 families have been reported: 83 species from the Aegean Sea, 63 species from the Sea of Marmara, 51 species from the Levantine Sea, and 2 species from the Black Sea. Among these species, 3 species are new records for the marine fauna of Turkey: Rhizaxinella elongata, Axinyssa digitata, and Terpios gelatinosa. Raspalia viminalis is a new record for the Sea of Marmara. The morphological and distributional features of 3 species are presented. In addition, a checklist of the sponge species reported from the Turkish coasts to date is provided. Key words: Sponge diversity, new records, species distribution, Black Sea, Aegean Sea, Sea of Marmara, Levantine Sea 1. Introduction compared to that of the other parts of the Mediterranean. The phylum Porifera (sponges) is known to be the most The oldest study on sponges of the coasts of Turkey dates primitive metazoan group and has 4 classes, namely back to 1885, when Colombo (1885) reported 5 sponge Calcarea (667 species in the world’s oceans), Hexactinellida species from the Çanakkale Strait.
    [Show full text]