Arctic and Antarctic Bryozoan Communities and Facies
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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. -
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 -
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. -
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. -
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. -
Recovery in Antarctic Benthos After Iceberg Disturbance: Trends in Benthic Composition, Abundance and Growth Forms
MARINE ECOLOGY PROGRESS SERIES Vol. 278: 1–16, 2004 Published September 7 Mar Ecol Prog Ser Recovery in Antarctic benthos after iceberg disturbance: trends in benthic composition, abundance and growth forms N. Teixidó1, 3,*, J. Garrabou2, J. Gutt1, W. E. Arntz1 1Alfred Wegener Institut für Polar- und Meeresforschung, Columbusstraße, 27568 Bremerhaven, Germany 2Marine d’Endoume, Centre d’Océanologie de Marseille, rue Batterie des Lions, 13007 Marseille, France 3Present address: Institut de Ciències del Mar (CMIMA-CSIC), Passeig Marítim de la Barceloneta 37–49, 08003 Barcelona, Spain ABSTRACT: The response of an Antarctic benthic community to iceberg disturbance was investi- gated using underwater photographs (1 m2 each) on the SE Weddell Sea shelf. This study: (1) char- acterises composition, coverage, number of patches and area of sessile benthic fauna, (2) describes faunal heterogeneity using MDS ordination and identifies ‘structural taxa’ of each recovery stage, and (3) analyses changes of growth-form patterns during Antarctic recovery. We observed changes in the space occupation of benthic organisms along the recolonisation stages. Uncovered sediment characterised the early stages ranging from 98 to 91% of the coverage. The later stages showed high (70.5%) and intermediate (52.5%) values of benthic coverage, where demosponges, bryozoans and ascidians exhibited a high number of patches and taxa. Several ‘structural species’ were identified among the stages, and information is provided on their coverage, number of patches and area. Over- all, maximum areas of patches increased as recovery proceeded. Early stages were characterised by the presence of pioneer taxa, which only partly covered the bottom sediment but were locally abun- dant (e.g. -
The Unique Skeleton of Siliceous Sponges (Porifera; Hexactinellida and Demospongiae) That Evolved first from the Urmetazoa During the Proterozoic: a Review” by W
Biogeosciences Discuss., 4, S262–S276, 2007 Biogeosciences www.biogeosciences-discuss.net/4/S262/2007/ BGD Discussions c Author(s) 2007. This work is licensed 4, S262–S276, 2007 under a Creative Commons License. Interactive Comment Interactive comment on “The unique skeleton of siliceous sponges (Porifera; Hexactinellida and Demospongiae) that evolved first from the Urmetazoa during the Proterozoic: a review” by W. E. G. Müller et al. W. E. G. Müller et al. Received and published: 3 April 2007 3rd April 2007 Full Screen / Esc From : Prof. Dr. W.E.G. Müller, Institut für Physiologische Chemie, Abteilung Ange- wandte Molekularbiologie, Universität, Duesbergweg 6, 55099 Mainz; GERMANY. tel.: Printer-friendly Version +49-6131-392-5910; fax.: +49-6131-392-5243; E-mail: [email protected] To the Editorial Board Interactive Discussion MS-NR: bgd-2006-0069 Discussion Paper S262 EGU Dear colleagues: BGD Thank you for your email from April 2nd informing me that our manuscript entitled: 4, S262–S276, 2007 The unique skeleton of siliceous sponges (Porifera; Hexactinellida and Demospongiae) that evolved first from the Urmetazoa during the Proterozoic: a review by: Werner E.G. Müller, Jinhe Li, Heinz C. Schröder, Li Qiao and Xiaohong Wang Interactive Comment which we submit for the Journal Biogeosciences must be revised. In the following we discuss point for point the arguments raised by the referees/reader. In detail: Interactive comment on “The unique skeleton of siliceous sponges (Porifera; Hex- actinellida and Demospongiae) that evolved first from the Urmetazoa during the Pro- terozoic: a review” by W. E. G. Müller et al. By: M. -
3D Chitin Scaffolds of Marine Demosponge
marine drugs Article 3D Chitin Scaffolds of Marine Demosponge Origin for Biomimetic Mollusk Hemolymph-Associated Biomineralization Ex-Vivo Marcin Wysokowski 1,2,* , Tomasz Machałowski 1,2 , Iaroslav Petrenko 2, Christian Schimpf 3, David Rafaja 3 , Roberta Galli 4, Jerzy Zi˛etek 5, Snežana Pantovi´c 6, Alona Voronkina 7 , Valentine Kovalchuk 8, Viatcheslav N. Ivanenko 9 , Bert W. Hoeksema 10,11 , Cristina Diaz 12, Yuliya Khrunyk 13,14 , Allison L. Stelling 15, Marco Giovine 16, Teofil Jesionowski 1 and Hermann Ehrlich 2,17,* 1 Faculty of Chemical Technology, Institute of Chemical Technology and Engineering, Poznan University of Technology, Berdychowo 4, 60965 Poznan, Poland; [email protected] (T.M.); teofi[email protected] (T.J.) 2 Institute of Electronics and Sensor Materials, TU Bergakademie Freiberg, Gustav-Zeuner str. 3, 09599 Freiberg, Germany; [email protected] 3 Institute of Materials Science, TU Bergakademie Freiberg, 09599 Freiberg, Germany; [email protected] (C.S.); [email protected] (D.R.) 4 Clinical Sensoring and Monitoring, Department of Anesthesiology and Intensive Care Medicine, Faculty of Medicine, TU Dresden, 01307 Dresden, Germany; [email protected] 5 Faculty of Veterinary Medicine, Department of Epizootiology and Clinic of Infectious Diseases, University of Life Sciences, Gł˛eboka30, 20612 Lublin, Poland; [email protected] 6 Faculty of Medicine, University of Montenegro, Kruševac bb, 81000 Podgorica, Montenegro; [email protected] 7 Department of Pharmacy, -
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. -
The Boundary Reefs: Glass Sponge (Porifera: Hexactinellidae) Reefs on the International Border Between Canada and the United States
NOAA Technical Memorandum NMFS-AFSC-264 The Boundary Reefs: Glass Sponge (Porifera: Hexactinellidae) Reefs on the International Border Between Canada and the United States by R. P. Stone, K. W. Conway, D. J. Csepp, J. V. Barrie U.S. DEPARTMENT OF COMMERCE National Oceanic and Atmospheric Administration National Marine Fisheries Service Alaska Fisheries Science Center January 2014 NOAA Technical Memorandum NMFS The National Marine Fisheries Service's Alaska Fisheries Science Center uses the NOAA Technical Memorandum series to issue informal scientific and technical publications when complete formal review and editorial processing are not appropriate or feasible. Documents within this series reflect sound professional work and may be referenced in the formal scientific and technical literature. The NMFS-AFSC Technical Memorandum series of the Alaska Fisheries Science Center continues the NMFS-F/NWC series established in 1970 by the Northwest Fisheries Center. The NMFS-NWFSC series is currently used by the Northwest Fisheries Science Center. This document should be cited as follows: Stone, R. P., K. W. Conway, D. J. Csepp, and J. V. Barrie. 2013. The boundary reefs: glass sponge (Porifera: Hexactinellida) reefs on the international border between Canada and the United States. U.S. Dep. Commer., NOAA Tech. Memo. NMFS-AFSC-264, 31 p. Document available: http://www.afsc.noaa.gov/Publications/AFSC-TM/NOAA-TM-AFSC-264.pdf Reference in this document to trade names does not imply endorsement by the National Marine Fisheries Service, NOAA. NOAA Technical Memorandum NMFS-AFSC-264 The Boundary Reefs: Glass Sponge (Porifera: Hexactinellidae) Reefs on the International Border Between Canada and the United States by R. -
Formation of Giant Spicules in the Deep-Sea Hexactinellid Monorhaphis Chuni (Schulze 1904): Electron-Microscopic and Biochemical Studies
Cell Tissue Res (2007) 329:363–378 DOI 10.1007/s00441-007-0402-x REGULAR ARTICLE Formation of giant spicules in the deep-sea hexactinellid Monorhaphis chuni (Schulze 1904): electron-microscopic and biochemical studies Werner E. G. Müller & Carsten Eckert & Klaus Kropf & Xiaohong Wang & Ute Schloßmacher & Christopf Seckert & Stephan E. Wolf & Wolfgang Tremel & Heinz C. Schröder Received: 25 November 2006 /Accepted: 19 February 2007 / Published online: 4 April 2007 # Springer-Verlag 2007 Abstract The siliceous sponge Monorhaphis chuni (Hexa- spicules; it harbors the axial filament and is surrounded by ctinellida) synthesizes the largest biosilica structures on an axial cylinder (100–150 μm) of electron-dense homo- earth (3 m). Scanning electron microscopy has shown that geneous silica. During dissolution of the spicules with these spicules are regularly composed of concentrically hydrofluoric acid, the axial filament is first released arranged lamellae (width: 3–10 μm). Between 400 and 600 followed by the release of a proteinaceous tubule. Two lamellae have been counted in one giant basal spicule. An major proteins (150 kDa and 35 kDa) have been visualized, axial canal (diameter: ~2 μm) is located in the center of the together with a 24-kDa protein that cross-reacts with antibodies against silicatein. The spicules are surrounded by a collagen net, and the existence of a hexactinellidan Carsten Eckert was previously with the Museum für Naturkunde, collagen gene has been demonstrated by cloning it from Invalidenstrasse 43, 10115 Berlin, Germany. Aphrocallistes vastus. During the axial growth of the The collagen sequence from Aphrocallistes vastus reported here, viz., spicules, silicatein or the silicatein-related protein is [COL_APHRO] APHVACOL (accession number AM411124), has been deposited in the EMBL/GenBank data base. -
An Upper Miocene Hexactinellid Sponge from the Puente Shale, Orange County, California J
J. Paleont., 70(6), 1996, pp. 908-913 Copyright © 1996, The Paleontological Society 0022-3360/96/0070-0908S03.00 AN UPPER MIOCENE HEXACTINELLID SPONGE FROM THE PUENTE SHALE, ORANGE COUNTY, CALIFORNIA J. KEITH RIGBY AND YVONNE ALBI Room 210 Page School, Department of Geology, Brigham Young University, Provo, Utah 84602, and 7001 Vista Del Mar Lane, Playa del Rey, California 90293 ABSTRACT—Well-preserved, laterally flattened, farreid hexactinellid sponges of the new species Farrea rugosa have been recently discovered in the upper Miocene Puente Shale in the Peralta Hills in southeastern Anaheim, Orange County, California. This is the first farreid sponge reported from the Miocene of California and is one of the few Miocene sponges reported from North America. The cluster is of upward bifurcating, moderately complex sponges in which branches are regularly rugose and skeletons are each a single layer of dictyid net, with aborted proximal and distal rays in the otherwise laterally fused quadruled skeleton of original silica. The sponges occur in pinkish brown sandy siltstone in the limited exposure beneath older alluvium that blankets much of the local area. INTRODUCTION nifera include several species of Bolivina d'Orbigny, 1839, and NEARLY COMPLETE cluster of laterally flattened farreid hex- single species of Eponides de Montfort, 1808, Pseudoparella A actinellid sponges has been collected from the Upper Mio- Cushman and Ten Dam, 1948, and Suggrunda Hoffmeister and cene Puente Shale, probably the Yorba Member, in the Peralta Berry, 1937, according to Richmond (1952). These beds were Hills area of eastern Anaheim, Orange County, California (Fig- exposed in a shallow ditch at the time the collections were made, ure 1).