A New Species Sponge Cliona Clionaidae) from The
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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). -
Growth Inhibition of Red Abalone (Haliotis Rufescens) Infested with an Endolithic Sponge (Cliona Sp.)
GROWTH INHIBITION OF RED ABALONE (HALIOTIS RUFESCENS) INFESTED WITH AN ENDOLITHIC SPONGE (CLIONA SP.) By Kirby Gonzalo Morejohn A Thesis Presented to The Faculty of Humboldt State University In Partial Fulfillment Of the Requirements for the Degree Master of Science In Natural Resources: Biology May, 2012 GROWTH INHIBITION OF RED ABALONE (HALIOTIS RUFESCENS) INFESTED WITH AN ENDOLITHIC SPONGE (CLIONA SP.) HUMBOLDT STATE UNIVERSITY By Kirby Gonzalo Morejohn We certify that we have read this study and that it conforms to acceptable standards of scholarly presentation and is fully acceptable, in scope and quality, as a thesis for the degree of Master of Science. ________________________________________________________________________ Dr. Sean Craig, Major Professor Date ________________________________________________________________________ Dr. Tim Mulligan, Committee Member Date ________________________________________________________________________ Dr. Frank Shaughnessy, Committee Member Date ________________________________________________________________________ Dr. Laura Rogers-Bennett, Committee Member Date ________________________________________________________________________ Dr. Michael Mesler, Graduate Coordinator Date ________________________________________________________________________ Dr. Jená Burges, Vice Provost Date ii ABSTRACT Understanding the effects of biotic and abiotic pressures on commercially important marine species is crucial to their successful management. The red abalone (Haliotis rufescensis) is a commercially -
Microbiome Structure of Ecologically Important Bioeroding Sponges (Family Clionaidae)
bioRxiv preprint doi: https://doi.org/10.1101/2020.01.28.923250; this version posted January 29, 2020. 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. 1 2 Microbiome structure of ecologically important bioeroding sponges (family Clionaidae): 3 The role of host phylogeny and environmental plasticity. 4 Oriol Sacristán-Soriano1,2, †, Xavier Turon2 and Malcolm Hill1,3 5 6 7 1Department of Biology; University of Richmond; Richmond, VA 8 2Centre d’Estudis Avançats de Blanes (CEAB, CSIC), Blanes, Spain 9 3Department of Biology, Bates College, Lewiston, ME 04240 10 †Corresponding author 11 12 13 Keywords: symbiosis, bioerosion, microbiome, Symbiodinium, Cliona, Spheciospongia, 14 Cervicornia 15 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.01.28.923250; this version posted January 29, 2020. 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. 16 Abstract 17 The potential of increased bioerosion by excavating sponges in future environmental scenarios 18 represents a potential threat to coral reef structure and function. If we are to predict changes to 19 coral reef habitats, it is important to understand the biology of these sponges. Little is known 20 about prokaryotic associations in excavating sponges despite the fact that evidence indicates they 21 contribute to the sponge growth through their heterotrophic metabolism and may even act as 22 microborers. Here, we provide the first detailed description of the microbial community of 23 multiple bioeroding sponges from the Clionaidae family (Cliona varians, C. -
Zootaxa: Cliona Minuscula, Sp. Nov. (Hadromerida : Clionaidae) And
Zootaxa 1312: 1–24 (2006) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1312 Copyright © 2006 Magnolia Press ISSN 1175-5334 (online edition) Cliona minuscula, sp. nov. (Hadromerida : Clionaidae) and other bioeroding sponges that only contain tylostyles CHRISTINE HANNA LYDIA SCHÖNBERG1, STEFANIE GRASS2 & ANKE TARJA HEIERMANN2 1Centre for Marine Studies, The University of Queensland, Brisbane, St. Lucia, QLD 4072, Australia; 2present address: Carl von Ossietzky Universität Oldenburg, Fakultät 5, Institut für Biologie und Umweltwissen- schaften, Abteilung Zoomorphologie und Systematik, 26111 Oldenburg, ph +49-(0)441-7983611, fax +49- (0)441-7983250. 2Carl von Ossietzky Universität Oldenburg, Fakultät 5, Institut für Biologie und Umweltwissenschaften, Abtei- lung Zoomorphologie und Systematik, 26111 Oldenburg, ph +49-(0)441-7983611, fax +49-(0)441-7983250. Abstract A new bioeroding sponge belonging to the genus Cliona is described from the Australian Great Barrier Reef, Cliona minuscula, sp. nov. As the sponge lacked microscleres, comparison with existing clionaid species was difficult. We considered 15 other species of Cliona with only tylostyles: C. alderi, C. arenosa. C. caesia nov. comb., C. californiana, C. celata, C. delitrix, C. dissimilis, C. ecaudis, C. insidiosa, C. janitrix, C. kempi, C. laticavicola, C. macgeachii, C. millepunctata and C. peponaca. Characters of all species are presented in table-form to facilitate comparison during future studies. We listed additional species of Cliona that were not directly compared to the new species, because they were either invalid, insufficiently described, or they may not be obligate bioeroders. The form and dimensions of the megascleres of C. minuscula, sp. nov. indicated that it is distinct from all considered species. -
Florida Keys Species List
FKNMS Species List A B C D E F G H I J K L M N O P Q R S T 1 Marine and Terrestrial Species of the Florida Keys 2 Phylum Subphylum Class Subclass Order Suborder Infraorder Superfamily Family Scientific Name Common Name Notes 3 1 Porifera (Sponges) Demospongia Dictyoceratida Spongiidae Euryspongia rosea species from G.P. Schmahl, BNP survey 4 2 Fasciospongia cerebriformis species from G.P. Schmahl, BNP survey 5 3 Hippospongia gossypina Velvet sponge 6 4 Hippospongia lachne Sheepswool sponge 7 5 Oligoceras violacea Tortugas survey, Wheaton list 8 6 Spongia barbara Yellow sponge 9 7 Spongia graminea Glove sponge 10 8 Spongia obscura Grass sponge 11 9 Spongia sterea Wire sponge 12 10 Irciniidae Ircinia campana Vase sponge 13 11 Ircinia felix Stinker sponge 14 12 Ircinia cf. Ramosa species from G.P. Schmahl, BNP survey 15 13 Ircinia strobilina Black-ball sponge 16 14 Smenospongia aurea species from G.P. Schmahl, BNP survey, Tortugas survey, Wheaton list 17 15 Thorecta horridus recorded from Keys by Wiedenmayer 18 16 Dendroceratida Dysideidae Dysidea etheria species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 19 17 Dysidea fragilis species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 20 18 Dysidea janiae species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 21 19 Dysidea variabilis species from G.P. Schmahl, BNP survey 22 20 Verongida Druinellidae Pseudoceratina crassa Branching tube sponge 23 21 Aplysinidae Aplysina archeri species from G.P. Schmahl, BNP survey 24 22 Aplysina cauliformis Row pore rope sponge 25 23 Aplysina fistularis Yellow tube sponge 26 24 Aplysina lacunosa 27 25 Verongula rigida Pitted sponge 28 26 Darwinellidae Aplysilla sulfurea species from G.P. -
Porifera, Demospongiae) from a Karst Lake in Ha Long Bay (Vietnam
Journal of Marine Science and Engineering Article A New Species of Spongilla (Porifera, Demospongiae) from a Karst Lake in Ha Long Bay (Vietnam) Barbara Calcinai 1,* , Carlo Cerrano 1,2 , Laura Núñez-Pons 2 , Maurizio Pansini 3, Do Cong Thung 4 and Marco Bertolino 3 1 Department of Life and Environmental Sciences, Università Politecnica delle Marche, 60131 Ancona, Italy; [email protected] 2 Department of Integrated Marine Ecology (EMI), Stazione Zoologica Anton Dohrn (SZN), 80121 Napoli, Italy; [email protected] 3 Department of Earth, Environmental and Life Sciences, University of Genova, 16132 Genova, Italy; [email protected] (M.P.); [email protected] (M.B.) 4 Institute of Marine Environment and Resources (IMER), Hai Phong City, Vietnam; [email protected] * Correspondence: [email protected]; Tel.: +39-071-2204283 Received: 26 October 2020; Accepted: 5 December 2020; Published: 9 December 2020 Abstract: Cahong in Ha Long Bay (Vietnam) is a small lake with a reduced, invisible connection with the open sea. The water column conditions locally experience notable fluctuations across the year, mostly driven by biannual monsoon seasons. Salinity, temperature, and pH often reach extreme values, unsustainable for the majority of the marine fauna. Therefore, the biodiversity of the benthic macrofauna in this peculiar habitat is remarkably low. In particular, a single sponge species new to science was found solely populating this characteristic brackish lake during our last survey in August 2018. Spongilla manconiae sp. nov. is a new Porifera species described here. It belongs to an exclusively freshwater taxon and seems to have acquired adaptive traits to tolerate extreme peaks of temperature and salinity. -
Life-History Traits of a Common Caribbean Coral-Excavating Sponge, Cliona Tenuis (Porifera: Hadromerida) Manuel González-Riveroa,B,G*, Alexander V
Journal of Natural History, 2013 http://dx.doi.org/10.1080/00222933.2013.802042 Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida) Manuel González-Riveroa,b,g*, Alexander V. Ereskovskyc , Christine H. L. Schönbergd , Renata Ferrarie,g, Jane Fromonte and Peter J. Mumbyb,g aCoral Reefs Ecosystems Laboratory, School of Biological Sciences, The University of Queensland. St Lucia campus, Brisbane. Qld 4072. Australia; bCollege of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom; cInstitut Méditerranéen de Biodiversité et d’Ecologie marine et continentale (IMBE), CNRS, Aix-Marseille Université, Marseille, France; dAustralian Institute of Marine Science, Oceans Institute at The University of Western Australia, Crawley, Australia; eCoastal & Marine Ecology Group, School of Biological Sciences, The University of Sydney, Australia; fWestern Australian Museum, Welshpool, Australia; gMarine Spatial Ecology Lab, School of Biological Sciences, University of Queensland. St Lucia Campus, Brisbane. Qld 4072. Australia (Received 3 June 2012; final version received 15 April 2013) Clionaids are important competitors and bio-eroding agents on coral reefs; how- ever, little is known of their biology. We studied aspects of life history of Cliona tenuis, in particular its sexual reproduction and growth. Temporal variations in these traits were studied over a year, in correlation with water temperature as a proxy for seasonality. Growth and sexual reproduction occurred at separate times and followed intra-annual variations in temperature. Growth increased during the warmest months of the year, reaching an average rate of 29.9 ± 6.7 mm dur- ing 286 days. Cliona tenuis is oviparous, and the results suggest gonochorism. -
A New Clionaid Sponge Infests Live Corals on the West Coast of India (Porifera,
Formatted ... Author Version : Systematics and Biodiversity, vol.17(2); 2019; 190-206 Formatted ... Formatted A new clionaid sponge infests live corals on the west coast of India (Porifera, ... Demospongiae, Clionaida) Formatted ... Formatted ... Formatted ... Sambhaji Mote1, Christine H.L. Schönberg2, Toufiek Samaai3,4, Vishal Gupta1, Baban Ingole*1 Formatted ... Formatted ... 1 CSIR–National Institute of Oceanography, Dona Paula, Goa, India Formatted ... 2 School of Earth and Environment and Oceans Institute, Indian Ocean Marine Research Centre, the Formatted ... University of Western Australia, Fairway Entrance 4, Crawley, WA 6009, Australia Formatted ... 3 Department of Environmental Affairs, Oceans and Coasts Branch, Oceans and Coasts Research Formatted ... Chief Directorate, Marine Biodiversity and Ecosystem Research Directorate, Private Bag X2, Formatted ... Roggebaai, 8012, Cape Town, Western Cape, South Africa. Formatted ... 4Marine Research Institute (MA-RE), University of Cape Town, Private Bag X3, Rondebosch, 7701, Formatted Cape Town, South Africa ... Formatted (*Corresponding author: [email protected]) ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted ... Formatted -
Sponge Mortality at Marathon and Long Key, Florida: Patterns of Species Response and Population Recovery
Sponge Mortality at Marathon and Long Key, Florida: Patterns of Species Response and Population Recovery JOHN M. STEVELY1*, DONALD E. SWEAT2, THERESA M. BERT3, CARINA SIM-SMITH4, and MICHELLE KELLY4 1Florida Sea Grant College Program, Marine Extension Program, 1303 Seventeenth Street West, Palmetto, Florida 34221 USA. *[email protected]. 2Florida Sea Grant College Program, Marine Extension Program, 830 First Street South, St. Petersburg, Florida 33701 USA. 3Florida Fish and Wildlife Conservation Commission, Fish and Wildlife Research Institute, 100 Eighth Avenue Southeast, St. Petersburg, Florida 33701 USA. 4National Centre for Aquatic Biodiversity and Biosecurity, National Institute of Water and Atmospheric Research Limited, Private Bag 109 695, New Market, Auckland, New Zealand. ABSTRACT In the early 1990s, widespread sponge mortality events occurred in the Florida Keys, USA. These mortality events were coincidental with successive blooms of the picoplanktonic cyanobacterium Synechococcus sp. Although the specific cause of sponge death remains unknown, we conclude that bloom conditions caused the death of these sponges. We documented the effects of the mortality events on sponge community biomass and followed the sponge population response of 23 species for up to 15 years (1991 - 2006). In doing so, we provide an unprecedented, long-term, and detailed view of sponge population dynamics in the Florida Keys, following a set of environmental conditions that caused widespread mortality. Abundance of many sponge species following the mortality events was dynamic and contrasts with work done on deep-water sponge communities that have shown such communities to be stable over long periods of time. Recovery of the sponge community biomass in the Florida Keys was slow, taking 10 - 15 years. -
Hadromerida, Clionaidae) from the Red Sea: a Taxonomical Challenge
Org Divers Evol (2010) 10:275–285 DOI 10.1007/s13127-010-0027-x ORIGINAL ARTICLE Two Pione species (Hadromerida, Clionaidae) from the Red Sea: a taxonomical challenge Filippo Ferrario & Barbara Calcinai & Dirk Erpenbeck & Paolo Galli & Gert Wörheide Received: 17 December 2009 /Accepted: 14 April 2010 /Published online: 24 June 2010 # Gesellschaft für Biologische Systematik 2010 Abstract Boring sponges of the genus Pione (Hadromerida, performed on spicules and micro-erosion patterns by Clionaidae) are easily recognizable due to their spiculation. means of both light and scanning electron microscopy. However, species identification is challenging, as the Two apparent morphotypes can be distinguished, mainly potentially diagnostic morphological character states of by the growth form, but statistical analysis does not different species often overlap. For this reason, this group support a clear separation in two species. In addition, a of species is frequently referred to as the ‘Pione vastifica DNA barcoding approach using sequences of CO1 has not complex’, after the most well-studied species of the genus. identified any nucleotide sequence differences. These data Boring-sponge samples were collected in the Red Sea and support the hypothesis that P. cf. lampa and P. cf. vastifica identified as P.cf.lampa and P.cf.vastifica, respectively. from the Red Sea are conspecific. So far, these two species names have usually been considered as valid, although some authors suggested Keywords Pione vastifica . Pione lampa . Boring sponges . them to be synonymous. Morphological analyses were Growth form . DNA barcoding : F. Ferrario P. Galli Introduction Dipartimento di Biotecnologie e Bioscienze, Università degli Studi di Milano-Bicocca, The genus Pione belongs to the family Clionaidae, which Piazza della Scienza, 20126 Milano, Italy comprises the majority of excavating sponges. -
Chemical and Mechanical Bioerosion of Boring Sponges from Mexican Pacific Coral Reefs
2827 The Journal of Experimental Biology 211, 2827-2831 Published by The Company of Biologists 2008 doi:10.1242/jeb.019216 Chemical and mechanical bioerosion of boring sponges from Mexican Pacific coral reefs Héctor Nava1,2,* and José Luis Carballo1 1Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México (UNAM), Avenida Joel Montes Camarena, s/n. apartado postal 811, 82000 Mazatlán, México and 2Posgrado en Ciencias del Mar y Limnología, ICML, UNAM, Mexico *Author for correspondence (e-mail: [email protected]) Accepted 7 July 2008 SUMMARY Species richness (S) and frequency of invasion (IF) by boring sponges on living colonies of Pocillopora spp. from National Park Isla Isabel (México, East Pacific Ocean) are presented. Twelve species belonging to the genera Aka, Cliona, Pione, Thoosa and Spheciospongia were found, and 56% of coral colonies were invaded by boring sponges, with Cliona vermifera Hancock 1867 being the most abundant species (30%). Carbonate dissolution rate and sediment production were quantified for C. vermifera and Cliona flavifodina Rützler 1974. Both species exhibited similar rates of calcium carbonate (CaCO3) dissolution (1.2±0.4 and –2 –1 –2 –1 0.5±0.2 kg CaCO3 m year , respectively, mean ± s.e.m.), and sediment production (3.3±0.6 and 4.6±0.5 kg CaCO3 m year ), –2 –1 resulting in mean bioerosion rates of 4.5±0.9 and 5.1±0.5 kg CaCO3 m year , respectively. These bioerosion rates are close to previous records of coral calcification per unit of area, suggesting that sponge bioerosion alone can promote disequilibrium in the reef accretion/destruction ratio in localities that are heavily invaded by boring sponges. -
Marine Invertebrate Biodiversity from the Argentine Sea, South Western Atlantic
A peer-reviewed open-access journal ZooKeys 791: 47–70Marine (2018) invertebrate biodiversity from the Argentine Sea, South Western Atlantic 47 doi: 10.3897/zookeys.791.22587 DATA PAPER http://zookeys.pensoft.net Launched to accelerate biodiversity research Marine invertebrate biodiversity from the Argentine Sea, South Western Atlantic Gregorio Bigatti1,2,3, Javier Signorelli1 1 Laboratorio de Reproducción y Biología Integrativa de Invertebrados Marinos, (LARBIM) IBIOMAR-CO- NICET. Bvd. Brown 2915 (9120) Puerto Madryn, Chubut, Argentina 2 Universidad Nacional de la Pata- gonia San Juan Bosco, Boulevard Brown 3051, Puerto Madryn, Chubut, Argentina 3 Facultad de Ciencias Ambientales, Universidad Espíritu Santo, Ecuador Corresponding author: Javier Signorelli ([email protected]) Academic editor: P. Stoev | Received 13 December 2017 | Accepted 7 September 2018 | Published 22 October 2018 http://zoobank.org/ECB902DA-E542-413A-A403-6F797CF88366 Citation: Bigatti G, Signorelli J (2018) Marine invertebrate biodiversity from the Argentine Sea, South Western Atlantic. ZooKeys 791: 47–70. https://doi.org/10.3897/zookeys.791.22587 Abstract The list of marine invertebrate biodiversity living in the southern tip of South America is compiled. In particular, the living invertebrate organisms, reported in the literature for the Argentine Sea, were checked and summarized covering more than 8,000 km of coastline and marine platform. After an exhaustive lit- erature review, the available information of two centuries of scientific contributions is summarized. Thus, almost 3,100 valid species are currently recognized as living in the Argentine Sea. Part of this dataset was uploaded to the OBIS database, as a product of the Census of Marine Life-NaGISA project.