Identification of Sponge Species

Total Page:16

File Type:pdf, Size:1020Kb

Identification of Sponge Species Identification of sponge species Species identification is important for ecological, evolutionary, systematic, and biodiversity studies, many of which contribute to the development of conservation and management plans. Many marine species can be identified using pictorial guides that highlight their main physical characteristics. However, there are also many marine species of lesser-known groups, such as sponges, that are hard to identify with photographs or illustrations due to their lack of complex morphological characters, and thus require specialized techniques. Identifying sponges taxonomic levels. For example, the classes of known sponges are separated based on these The identification of sponges is very difficult due to characteristics: the Calcarea have calcium carbonate their unique morphological traits and intraspecific spicules, the Hexactinellida, siliceous spicules and variability in shape and colour. Therefore, proper the Demospongiae, siliceous spicules and sponging identification often requires collection and fibres or both. microscopic examination of their skeleton. Still, many observable morphological characters can Common features used to identify sponges are the be used to aid in sponge identification including following: overall shape, distribution of surface pores, colour, texture and size. Knowledge of other non- 0 Spongin fibres – organic skeletal elements made morphological characteristics, such as the ecological of collagen and forming very complex networks in traits of the different species can also be useful in many sponges. sponge identification. Several tools, such as posters 0 Dispersed collagen filaments – skeletal material and field guides, and designed to be used by found in all sponges non-specialist individuals while at sea have been 0 Spicules – inorganic elements present in almost developed. A selection of these is provided in the FAO all sponges’ skeleton and made of either calcium Vulnerable Marine Ecosystems webpage (www.fao. carbonate or silica. org/in-action/vulnerable-marine-ecosystems/ background/vme-tools/en/). New tools, including The composition, geometry and arrangement of the ones developed through SponGES will be these components can be diagnostic at different incorporated in the FAO VME webpage. SponGES has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 679849. This document reflects only the author’s view – the Executive Agency for Small and Medium- sized Enterprises is not responsible for any use that may be made of the information it contains. A selection of sponge identification tools DEEP–SEA SPONGES OF THE INDIAN OCEAN DEEP-SEA SPONGES OF THE MEDITERRANEAN SEA SPONGES SILICEOUS SPONGES – CLASS DEMOSPONGIAE GLASS SPONGES – CLASS HEXACTINELLIDA SPONGES SILICEOUS SPONGES – CLASS DEMOSPONGIAE GLASS SPONGES – CLASS HEXACTINELLIDA (PHYLUM Demosponges, also known as siliceous sponges, represent the largest and most diverse class within Porifera, comprising 85%, more than 6 600, of all sponge species. Their shape and size range from thin crusts, to various sizes Hexactinellids, also known as glass sponges, constitute a predominantly Demospongiae come in an enormous variety of shapes and sizes, from thinly encrusting masses, hemispheres, spheres, tiny globes and Hexactinellid glass sponges are unique amongst sponges in that they lack cell membranes and their silica spicules are based on a PORIFERA) of globular, vase-, cushion-, tree-like and giant barrels more than 2 m high. Coloration, derived from pigments or symbiotic associates, covers a wide spectrum (from white to black) including yellow, orange, red, blue, green, deep-sea group, typically occurring at bathyal and abyssal depths (i.e. below (PHYLUM lollipops, to large volcano-like forms several metres high. Others resemble flasks and tall tubes, or have fan and tree-like forms. Coloration hexagonal (six-rayed) design. Spicules may be extremely large as in a 'fishing-rod', or may be twisted into 'rope', fused into a network, or purple, brown, etc. Consistency depends on the skeletal composition and varies between soft, compressible, elastic, to tough and rock hard. The surface texture varies from smooth, velvety to rugose, and hispid. Approximately 200 m). They are exclusively marine and comprise approximately 675 species is derived from carotenoid pigments (purple, magenta, blue, brown, red, pink, orange, ochre and yellow), or due to the presence of form a soggy paper or rough sack-like fabric. Glass sponges are diverse in their shape: woven baskets and tubes, big sacks, fibreglass-like Sponges are amongst 670 demosponge species are known to occur in the Mediterranean Sea. worldwide, of which nine occur in the Mediterranean Sea. Their external PORIFERA) symbionts or specific metabolites. Texture reflects the underlying mineral (spicule) and organic (collagen, fibre) skeleton and may be matting, soft tulips on stalks, and hollow and solid coral-like sticks. Texture may be stony, softly papery, brittle, fragile; always non- the most ancient animals morphology usually varies between vase, blade, cup or tube-shaped and both Massive, hard sponges (Geodia spp.) Globular sponges with rooting structures (Thenea muricata) Lollipop sponges fleshy, woody, stony or fibrous. Demosponge skeletons may include spicules, sand grains, collagen and fibre, in various combinations. elastic. Coloration is muted, being translucent, white, cream, to faint pastel pinks and blues. to have appeared in the stalked and non-stalked forms exist. They attach to hard bottom using a basal Sponges are common disc or anchoring spicules, or to soft sediment by means of root-like structures. world’s oceans. Currently, Massive sponges Globular to egg- Lollipop-shaped invertebrates in the Monorhaphis chuni coming in a variety of shaped sponges sponges with Coloration is mostly in shades of white, beige and yellow. Ancorinidae species Cladorhizidae species Hyalonematidae species more than 8 000 species deep sea, providing shapes, from irregular with one or few a large, circular are recognized but over to convoluted masses; apical oscules. They (Stylocordyla Birds’ nest sponge (Pheronema carpenteri) habitat for certain 25 000 are estimated to younger specimens are are characterized pellita) to oval and usually (sub)spherical. by a distinct apically compressed Globular to sub- benthic fauna. exist. They are distributed Oscules are grouped groove around the (Rhizaxinella cylindrical sponges together and located mid-section of the pyrifera) “head” and possessing a wide and They attach to hard at all depths and latitudes, in depression areas body, where inhalant a slender stalk. One deep atrial cavity with and in some areas form located on the top pores (ostia) are substrate on oscule is visible at a large apical oscule. surface of the sponge. located, and root-like highly structured habitats the top of the head. The surface is “hairy” seamounts, Small inhalant pores structures projecting Thenea muricata Stelletta rugosa Stelletta sp. Ecionemia sp. Stelletta lithodes Abyssocladia sp. Asbestopluma sp. Chondrocladia spp. Hyalonema spp. Chalaronema sp. Dredged ‘glass rope’ Monorhaphis chuni Geodia barretti Geodia cydonium S. pellita, grey or Stylocordyla pellita Rhizaxinella pyrifera and shows an intricate known as sponge grounds, (ostia) are also grouped from the base, by hydrothermal vents, cream in colour, has a smooth and flexible stalk, and is attached to hard substrates by means of network of spicules. Size: ~ 10 to 40 cm Ø Depth: 1–2800 m Size: several mm high to ~ 30 cm high Depth: 60–2930 m Size: up to ~ 40 cm high Depth: 198–4077 m Size: 10 cm long (2 mm Ø) to 3 m long (1 cm Ø) Depth: 1567–2550 m aggregations, gardens or together but found distributed across the overall surface. G. barretti, cream in colour, has an even means of which they attach to soft substrate. Consistency is slightly compressible and texture is Texture is fibrous and and clean surface with a rubbery texture. G. cydonium, yellow in colour, has a hispid/harsh surface a rounded disc while R. pyrifera, dull yellow, has an occasionally knobbed or branched rigid stalk, pinnacles and canyons, smooth. Colour is white to brownish/greyish. compressible. It is Massive, flattened spherical to bowl-shaped sponges, with a smooth, granular or Feather-, tree-, sunflower- or lollipop-shaped 'carnivorous' sponges, with 'sticky' Tulip-shaped sponges with a large, cup-shaped to elongate body on a stem of glass Fishing rod-shaped sponge, comprising a single, massive spicule. A papery body clings reefs, particularly so in the often covered with sediment. Both species have a tough but slightly compressible consistency. and lives in soft sediment thanks to a branching root-like structure. hard corals, or anchor roughened, hairy surface. Oscules usually grouped at apex. Texture usually tough, filaments or balloon-shaped spheres on which living 'food' is caught. Attached by a threads, resembling a twisted rope that roots the sponge into sediment. Glass rope to the upper portion of the spicule that roots the sponge into soft sediment. Texture deep-sea. These habitats attached to the substrate incompressible. Skeleton dominated by harsh spicules that radiate internally and 'root' in soft substrate or by a rounded disc to hard substrate. Texture soft, often the only part collected. Texture of body soggy when wet, crisp and fibrous of body soggy when wet, fibrous and fragile when dry; easily detached. Colour of Size: up to 50 cm in diameter Depth
Recommended publications
  • Spicule Formation in Calcareous Sponges: Coordinated Expression
    www.nature.com/scientificreports OPEN Spicule formation in calcareous sponges: Coordinated expression of biomineralization genes and Received: 17 November 2016 Accepted: 02 March 2017 spicule-type specific genes Published: 13 April 2017 Oliver Voigt1, Maja Adamska2, Marcin Adamski2, André Kittelmann1, Lukardis Wencker1 & Gert Wörheide1,3,4 The ability to form mineral structures under biological control is widespread among animals. In several species, specific proteins have been shown to be involved in biomineralization, but it is uncertain how they influence the shape of the growing biomineral and the resulting skeleton. Calcareous sponges are the only sponges that form calcitic spicules, which, based on the number of rays (actines) are distinguished in diactines, triactines and tetractines. Each actine is formed by only two cells, called sclerocytes. Little is known about biomineralization proteins in calcareous sponges, other than that specific carbonic anhydrases (CAs) have been identified, and that uncharacterized Asx-rich proteins have been isolated from calcitic spicules. By RNA-Seq and RNA in situ hybridization (ISH), we identified five additional biomineralization genes inSycon ciliatum: two bicarbonate transporters (BCTs) and three Asx-rich extracellular matrix proteins (ARPs). We show that these biomineralization genes are expressed in a coordinated pattern during spicule formation. Furthermore, two of the ARPs are spicule- type specific for triactines and tetractines (ARP1 orSciTriactinin ) or diactines (ARP2 or SciDiactinin). Our results suggest that spicule formation is controlled by defined temporal and spatial expression of spicule-type specific sets of biomineralization genes. By the process of biomineralization many animal groups produce mineral structures like skeletons, shells and teeth. Biominerals differ in shape considerably from their inorganic mineral counterparts1.
    [Show full text]
  • Bryozoan Studies 2019
    BRYOZOAN STUDIES 2019 Edited by Patrick Wyse Jackson & Kamil Zágoršek Czech Geological Survey 1 BRYOZOAN STUDIES 2019 2 Dedication This volume is dedicated with deep gratitude to Paul Taylor. Throughout his career Paul has worked at the Natural History Museum, London which he joined soon after completing post-doctoral studies in Swansea which in turn followed his completion of a PhD in Durham. Paul’s research interests are polymatic within the sphere of bryozoology – he has studied fossil bryozoans from all of the geological periods, and modern bryozoans from all oceanic basins. His interests include taxonomy, biodiversity, skeletal structure, ecology, evolution, history to name a few subject areas; in fact there are probably none in bryozoology that have not been the subject of his many publications. His office in the Natural History Museum quickly became a magnet for visiting bryozoological colleagues whom he always welcomed: he has always been highly encouraging of the research efforts of others, quick to collaborate, and generous with advice and information. A long-standing member of the International Bryozoology Association, Paul presided over the conference held in Boone in 2007. 3 BRYOZOAN STUDIES 2019 Contents Kamil Zágoršek and Patrick N. Wyse Jackson Foreword ...................................................................................................................................................... 6 Caroline J. Buttler and Paul D. Taylor Review of symbioses between bryozoans and primary and secondary occupants of gastropod
    [Show full text]
  • Trophic Interactions Within the Ross Sea Continental Shelf Ecosystem Walker O
    Phil. Trans. R. Soc. B (2007) 362, 95–111 doi:10.1098/rstb.2006.1956 Published online 6 December 2006 Trophic interactions within the Ross Sea continental shelf ecosystem Walker O. Smith Jr1,*, David G. Ainley2 and Riccardo Cattaneo-Vietti3 1Virginia Institute of Marine Sciences, College of William and Mary, Gloucester Point, VA 23062, USA 2H.T. Harvey and Associates, 3150 Almaden Expressway, Suite 145, San Jose, CA 95118, USA 3Dipartimento per lo Studio del Territorio e delle sue Risorse, Universita` di Genova, Corso Europa 26, 16132 Genova, Italy The continental shelf of the Ross Sea is one of the Antarctic’s most intensively studied regions. We review the available data on the region’s physical characteristics (currents and ice concentrations) and their spatial variations, as well as components of the neritic food web, including lower and middle levels (phytoplankton, zooplankton, krill, fishes), the upper trophic levels (seals, penguins, pelagic birds, whales) and benthic fauna. A hypothetical food web is presented. Biotic interactions, such as the role of Euphausia crystallorophias and Pleuragramma antarcticum as grazers of lower levels and food for higher trophic levels, are suggested as being critical. The neritic food web contrasts dramatically with others in the Antarctic that appear to be structured around the keystone species Euphausia superba. Similarly, we suggest that benthic–pelagic coupling is stronger in the Ross Sea than in most other Antarctic regions. We also highlight many of the unknowns within the food web, and discuss the impacts of a changing Ross Sea habitat on the ecosystem. Keywords: Ross Sea; neritic food web; bio-physical coupling; ecosystem function; ecosystem structure; pelagic–benthic coupling 1.
    [Show full text]
  • Sponge–Microbe Interactions on Coral Reefs: Multiple Evolutionary Solutions to a Complex Environment
    fmars-08-705053 July 14, 2021 Time: 18:29 # 1 REVIEW published: 20 July 2021 doi: 10.3389/fmars.2021.705053 Sponge–Microbe Interactions on Coral Reefs: Multiple Evolutionary Solutions to a Complex Environment Christopher J. Freeman1*, Cole G. Easson2, Cara L. Fiore3 and Robert W. Thacker4,5 1 Department of Biology, College of Charleston, Charleston, SC, United States, 2 Department of Biology, Middle Tennessee State University, Murfreesboro, TN, United States, 3 Department of Biology, Appalachian State University, Boone, NC, United States, 4 Department of Ecology and Evolution, Stony Brook University, Stony Brook, NY, United States, 5 Smithsonian Tropical Research Institute, Panama City, Panama Marine sponges have been successful in their expansion across diverse ecological niches around the globe. Pioneering work attributed this success to both a well- developed aquiferous system that allowed for efficient filter feeding on suspended organic matter and the presence of microbial symbionts that can supplement host Edited by: heterotrophic feeding with photosynthate or dissolved organic carbon. We now know Aldo Cróquer, The Nature Conservancy, that sponge-microbe interactions are host-specific, highly nuanced, and provide diverse Dominican Republic nutritional benefits to the host sponge. Despite these advances in the field, many current Reviewed by: hypotheses pertaining to the evolution of these interactions are overly generalized; these Ryan McMinds, University of South Florida, over-simplifications limit our understanding of the evolutionary processes shaping these United States symbioses and how they contribute to the ecological success of sponges on modern Alejandra Hernandez-Agreda, coral reefs. To highlight the current state of knowledge in this field, we start with seminal California Academy of Sciences, United States papers and review how contemporary work using higher resolution techniques has Torsten Thomas, both complemented and challenged their early hypotheses.
    [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]
  • 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]
  • 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]
  • Effects of Agelas Oroides and Petrosia Ficiformis Crude Extracts on Human Neuroblastoma Cell Survival
    161-169 6/12/06 19:46 Page 161 INTERNATIONAL JOURNAL OF ONCOLOGY 30: 161-169, 2007 161 Effects of Agelas oroides and Petrosia ficiformis crude extracts on human neuroblastoma cell survival CRISTINA FERRETTI1*, BARBARA MARENGO2*, CHIARA DE CIUCIS3, MARIAPAOLA NITTI3, MARIA ADELAIDE PRONZATO3, UMBERTO MARIA MARINARI3, ROBERTO PRONZATO1, RENATA MANCONI4 and CINZIA DOMENICOTTI3 1Department for the Study of Territory and its Resources, University of Genoa, Corso Europa 26, I-16132 Genoa; 2G. Gaslini Institute, Gaslini Hospital, Largo G. Gaslini 5, I-16148 Genoa; 3Department of Experimental Medicine, University of Genoa, Via Leon Battista Alberti 2, I-16132 Genoa; 4Department of Zoology and Evolutionistic Genetics, University of Sassari, Via Muroni 25, I-07100 Sassari, Italy Received July 28, 2006; Accepted September 20, 2006 Abstract. Among marine sessile organisms, sponges (Porifera) Introduction are the major producers of bioactive secondary metabolites that defend them against predators and competitors and are used to Sponges (Porifera) are a type of marine fauna that produce interfere with the pathogenesis of many human diseases. Some bioactive molecules to defend themselves from predators or of these biological active metabolites are able to influence cell spatial competitors (1,2). It has been demonstrated that some survival and death, modifying the activity of several enzymes of these metabolites have a biomedical potential (3) and in involved in these cellular processes. These natural compounds particular, Ara-A and Ara-C are clinically used as antineoplastic show a potential anticancer activity but the mechanism of drugs (4,5) in the routine treatment of patients with leukaemia this action is largely unknown.
    [Show full text]
  • (1104L) Animal Kingdom Part I
    (1104L) Animal Kingdom Part I By: Jeffrey Mahr (1104L) Animal Kingdom Part I By: Jeffrey Mahr Online: < http://cnx.org/content/col12086/1.1/ > OpenStax-CNX This selection and arrangement of content as a collection is copyrighted by Jerey Mahr. It is licensed under the Creative Commons Attribution License 4.0 (http://creativecommons.org/licenses/by/4.0/). Collection structure revised: October 17, 2016 PDF generated: October 17, 2016 For copyright and attribution information for the modules contained in this collection, see p. 58. Table of Contents 1 (1104L) Animals introduction ....................................................................1 2 (1104L) Characteristics of Animals ..............................................................3 3 (1104L)The Evolutionary History of the Animal Kingdom ..................................11 4 (1104L) Phylum Porifera ........................................................................23 5 (1104L) Phylum Cnidaria .......................................................................31 6 (1104L) Phylum Rotifera & Phylum Platyhelminthes ........................................45 Glossary .............................................................................................53 Index ................................................................................................56 Attributions .........................................................................................58 iv Available for free at Connexions <http://cnx.org/content/col12086/1.1> Chapter 1 (1104L) Animals introduction1
    [Show full text]
  • Review of the Mineralogy of Calcifying Sponges
    Dickinson College Dickinson Scholar Faculty and Staff Publications By Year Faculty and Staff Publications 12-2013 Not All Sponges Will Thrive in a High-CO2 Ocean: Review of the Mineralogy of Calcifying Sponges Abigail M. Smith Jade Berman Marcus M. Key, Jr. Dickinson College David J. Winter Follow this and additional works at: https://scholar.dickinson.edu/faculty_publications Part of the Paleontology Commons Recommended Citation Smith, Abigail M.; Berman, Jade; Key,, Marcus M. Jr.; and Winter, David J., "Not All Sponges Will Thrive in a High-CO2 Ocean: Review of the Mineralogy of Calcifying Sponges" (2013). Dickinson College Faculty Publications. Paper 338. https://scholar.dickinson.edu/faculty_publications/338 This article is brought to you for free and open access by Dickinson Scholar. It has been accepted for inclusion by an authorized administrator. For more information, please contact [email protected]. © 2013. Licensed under the Creative Commons http://creativecommons.org/licenses/by- nc-nd/4.0/ Elsevier Editorial System(tm) for Palaeogeography, Palaeoclimatology, Palaeoecology Manuscript Draft Manuscript Number: PALAEO7348R1 Title: Not all sponges will thrive in a high-CO2 ocean: Review of the mineralogy of calcifying sponges Article Type: Research Paper Keywords: sponges; Porifera; ocean acidification; calcite; aragonite; skeletal biomineralogy Corresponding Author: Dr. Abigail M Smith, PhD Corresponding Author's Institution: University of Otago First Author: Abigail M Smith, PhD Order of Authors: Abigail M Smith, PhD; Jade Berman, PhD; Marcus M Key Jr, PhD; David J Winter, PhD Abstract: Most marine sponges precipitate silicate skeletal elements, and it has been predicted that they would be among the few "winners" in an acidifying, high-CO2 ocean.
    [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]
  • Macroscopic Characteristics Facilitate Identification of Common
    Polar Biology (2020) 43:91–110 https://doi.org/10.1007/s00300-019-02612-2 ORIGINAL PAPER Macroscopic characteristics facilitate identifcation of common Antarctic glass sponges (Porifera, Hexactinellida, Rossellidae) Luisa Federwisch1,2 · Dorte Janussen3 · Claudio Richter1,2 Received: 21 June 2019 / Revised: 8 December 2019 / Accepted: 10 December 2019 / Published online: 21 January 2020 © The Author(s) 2020 Abstract Glass sponges (Porifera, Hexactinellida) are conspicuous habitat-forming members of many Antarctic shelf communities. Despite their ecological importance, in-situ species identification remains problematic as it is traditionally based on micro- scopic analysis of spicules. External morphological features, in contrast, have largely been disregarded, so that different species have been mislabeled or lumped together when their identification was based on image material. In this paper, we provide a straight-forward guideline for in-situ identification of the most common rossellid sponges of the Antarctic shelf based on macroscopic characteristics. To determine diagnostic macroscopic characteristics of Anoxycalyx (Scolymastra) joubini and eight Rossella species, we combined examination of trawl-collected specimens, previous species descriptions and in-situ image material from the eastern Weddell Sea. Our study revealed that the smooth-walled species A. joubini, R. nuda and R. vanhoeffeni, previously often mixed up, can be distinguished by the form of their basal spicule tuft, their surface structure and their overall body form. The previously synonymized species R. racovitzae and R. podagrosa can be distinguished by their markedly different habitus. Based on our results, the so-called ‘R. racovitzae budding type’ in fact refers to R. podagrosa which occurs regularly in the eastern Weddell Sea.
    [Show full text]