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Annelida, Oligochaeta) from the Island of Elba (Italy)
Org. Divers. Evol. 2, 289–297 (2002) © Urban & Fischer Verlag http://www.urbanfischer.de/journals/ode Taxonomy and new bacterial symbioses of gutless marine Tubificidae (Annelida, Oligochaeta) from the Island of Elba (Italy) Olav Giere1,*, Christer Erséus2 1 Zoologisches Institut und Zoologisches Museum, Universität Hamburg, Germany 2 Department of Invertebrate Zoology, Swedish Museum of Natural History, Stockholm Received 15 April 2002 · Accepted 9 July 2002 Abstract In shallow sublittoral sediments of the north-west coast of the Island of Elba, Italy, a new gutless marine oligochaete, Olavius ilvae n. sp., was found together with a congeneric but not closely related species, O. algarvensis Giere et al., 1998. In diagnostic features of the genital organs, the new species differs from other Olavius species in having bipartite atria and very long, often folded spermathecae, but lacking penial chaetae.The Elba form of O. algarvensis has some structural differences from the original type described from the Algarve coast (Portugal).The two species from Elba share characteristics not previously reported for gutless oligochaetes: the lumen of the body cavity is unusually constrict- ed and often filled with chloragocytes, and the symbiotic bacteria are often enclosed in vacuoles of the epidermal cells. Regarding the bacterial ultrastructure, the species share three similar morphotypes as symbionts; additionally, in O. algarvensis a rare fourth type was found.The diver- gence of the symbioses in O. algarvensis, and the coincidence in structural -
Phylogenetic and Functional Characterization of Symbiotic Bacteria in Gutless Marine Worms (Annelida, Oligochaeta)
Phylogenetic and functional characterization of symbiotic bacteria in gutless marine worms (Annelida, Oligochaeta) Dissertation zur Erlangung des Grades eines Doktors der Naturwissenschaften -Dr. rer. nat.- dem Fachbereich Biologie/Chemie der Universität Bremen vorgelegt von Anna Blazejak Oktober 2005 Die vorliegende Arbeit wurde in der Zeit vom März 2002 bis Oktober 2005 am Max-Planck-Institut für Marine Mikrobiologie in Bremen angefertigt. 1. Gutachter: Prof. Dr. Rudolf Amann 2. Gutachter: Prof. Dr. Ulrich Fischer Tag des Promotionskolloquiums: 22. November 2005 Contents Summary ………………………………………………………………………………….… 1 Zusammenfassung ………………………………………………………………………… 2 Part I: Combined Presentation of Results A Introduction .…………………………………………………………………… 4 1 Definition and characteristics of symbiosis ...……………………………………. 4 2 Chemoautotrophic symbioses ..…………………………………………………… 6 2.1 Habitats of chemoautotrophic symbioses .………………………………… 8 2.2 Diversity of hosts harboring chemoautotrophic bacteria ………………… 10 2.2.1 Phylogenetic diversity of chemoautotrophic symbionts …………… 11 3 Symbiotic associations in gutless oligochaetes ………………………………… 13 3.1 Biogeography and phylogeny of the hosts …..……………………………. 13 3.2 The environment …..…………………………………………………………. 14 3.3 Structure of the symbiosis ………..…………………………………………. 16 3.4 Transmission of the symbionts ………..……………………………………. 18 3.5 Molecular characterization of the symbionts …..………………………….. 19 3.6 Function of the symbionts in gutless oligochaetes ..…..…………………. 20 4 Goals of this thesis …….………………………………………………………….. -
Envall Et Al
Molecular Phylogenetics and Evolution 40 (2006) 570–584 www.elsevier.com/locate/ympev Molecular evidence for the non-monophyletic status of Naidinae (Annelida, Clitellata, TubiWcidae) Ida Envall a,b,c,¤, Mari Källersjö c, Christer Erséus d a Department of Zoology, Stockholm University, SE-106 91 Stockholm, Sweden b Department of Invertebrate Zoology, Swedish Museum of Natural History, Box 50007, SE-104 05 Stockholm, Sweden c Laboratory of Molecular Systematics, Swedish Museum of Natural History, Box 50007, SE-104 05 Stockholm, Sweden d Department of Zoology, Göteborg University, Box 463, SE-405 30 Göteborg, Sweden Received 24 October 2005; revised 9 February 2006; accepted 15 March 2006 Available online 8 May 2006 Abstract Naidinae (former Naididae) is a group of small aquatic clitellate annelids, common worldwide. In this study, we evaluated the phylo- genetic status of Naidinae, and examined the phylogenetic relationships within the group. Sequence data from two mitochondrial genes (12S rDNA and 16S rDNA), and one nuclear gene (18S rDNA), were used. Sequences were obtained from 27 naidine species, 24 species from the other tubiWcid subfamilies, and Wve outgroup taxa. New sequences (in all 108) as well as GenBank data were used. The data were analysed by parsimony and Bayesian inference. The tree topologies emanating from the diVerent analyses are congruent to a great extent. Naidinae is not found to be monophyletic. The naidine genus Pristina appears to be a derived group within a clade consisting of several genera (Ainudrilus, Epirodrilus, Monopylephorus, and Rhyacodrilus) from another tubiWcid subfamily, Rhyacodrilinae. These results dem- onstrate the need for a taxonomic revision: either Ainudrilus, Epirodrilus, Monopylephorus, and Rhyacodrilus should be included within Naidinae, or Pristina should be excluded from this subfamily. -
1 Current and Selected Bibliographies on Benthic Biology – 2015 & 2016 –
1 ================================================================================== CURRENT AND SELECTED BIBLIOGRAPHIES ON BENTHIC BIOLOGY – 2015 & 2016 – [ published in May 2017 ] -------------------------------------------------------------------------------------------------------------------------------------------- FOREWORD. “Current and Selected Bibliographies on Benthic Biology” is published annually for the members of the Society for Freshwater Science (SFS) (formerly, the Midwest Benthological Society [MBS, 1953-1975] then the North American Benthological Society [NABS, 1975-2011]). This compilation summarizes titles of articles published in 2015. Additionally, pertinent titles of articles published prior to 2015 also have been included if they had not been cited in previous reviews (or to correct errors in previous annual bibliographies), and authors of several sections have also included citations for recent (2016 and 2017) publications. I extend my appreciation to 1) past and present members of the MBS, NABS and SFS Literature Review and Publications Committees and the Society presidents and treasurer Mike Swift for their support, 2) librarians Elizabeth Wohlgemuth (Illinois Natural History Survey) and Susan Braxton (Prairie Research Institute) for their assistance in accessing journals, other publications, bibliographic search engines and abstracting resources, and rare publications critical to the compilation and verification of citations included herein, and 3) Kristi L. Moss (Illinois Natural History Survey) for her assistance -
Phylogeny of 16S Rrna, Ribulose 1,5-Bisphosphate Carboxylase/Oxygenase, and Adenosine 5Ј-Phosphosulfate Reductase Genes from Gamma
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Aug. 2006, p. 5527–5536 Vol. 72, No. 8 0099-2240/06/$08.00ϩ0 doi:10.1128/AEM.02441-05 Copyright © 2006, American Society for Microbiology. All Rights Reserved. Phylogeny of 16S rRNA, Ribulose 1,5-Bisphosphate Carboxylase/Oxygenase, and Adenosine 5Ј-Phosphosulfate Reductase Genes from Gamma- and Alphaproteobacterial Symbionts in Gutless Marine Worms Downloaded from (Oligochaeta) from Bermuda and the Bahamas Anna Blazejak,1 Jan Kuever,1† Christer Erse´us,2 Rudolf Amann,1 and Nicole Dubilier1* Max Planck Institute of Marine Microbiology, Celsiusstrasse 1, D-28359 Bremen, Germany,1 and Department of Zoology, Go¨teborg University, Box 463, SE-405 30 Go¨teborg, Sweden2 Received 16 October 2005/Accepted 17 April 2006 Gutless oligochaetes are small marine worms that live in obligate associations with bacterial endosymbionts. http://aem.asm.org/ While symbionts from several host species belonging to the genus Olavius have been described, little is known of the symbionts from the host genus Inanidrilus. In this study, the diversity of bacterial endosymbionts in Inanidrilus leukodermatus from Bermuda and Inanidrilus makropetalos from the Bahamas was investigated using comparative sequence analysis of the 16S rRNA gene and fluorescence in situ hybridization. As in all other gutless oligochaetes examined to date, I. leukodermatus and I. makropetalos harbor large, oval bacteria identified as Gamma 1 symbionts. The presence of genes coding for ribulose-1,5-bisphosphate carboxylase/oxygenase form I (cbbL) and adenosine 5-phosphosulfate reductase (aprA) supports earlier studies indicating that these symbionts are chemoautotrophic sulfur oxidizers. Alphaproteobacteria, previously identified only in the gutless oligochaete Olavius loisae from the southwest Pacific Ocean, coexist with the Gamma 1 symbionts in both I. -
Fidelity Varies in the Symbiosis Between a Gutless Marine Worm and Its Microbial Consortium
bioRxiv preprint doi: https://doi.org/10.1101/2021.01.30.428904; this version posted January 30, 2021. 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 Fidelity varies in the symbiosis between a gutless marine worm and its microbial consortium 2 3 Yui Sato*1, Juliane Wippler1, Cecilia Wentrup2, Rebecca Ansorge1, Miriam Sadowski1, Harald 4 Gruber-Vodicka1, Nicole Dubilier*1, Manuel Kleiner*3 5 1Max Planck Institute for Marine Microbiology, Celsiusstr. 1, D-28359 Bremen, Germany 6 2University of Vienna, Department of Microbiology and Ecosystem Science, Althanstr. 14, A-1090 Vienna, Austria 7 3Department of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, USA 8 9 *Corresponding authors: 10 Yui Sato: [email protected], phone +49 (421) 2028-8240 11 Nicole Dubilier: [email protected], phone +49 (421) 2028 9320 12 Manuel Kleiner: [email protected], phone +1 919 515 3792 13 14 Keywords: microbiome, microbiota, animal-bacterial symbiosis, host-symbiont specificity, partner 15 fidelity, symbiont transmission, phylogenetic congruence, single nucleotide polymorphisms (SNPs), 16 intraspecific genetic variation 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.01.30.428904; this version posted January 30, 2021. 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. 17 Abstract 18 In obligate symbioses, partner fidelity plays a central role in maintaining the stability of the 19 association across multiple host generations. Fidelity has been well studied in hosts with a very 20 restricted diversity of symbionts, but little is known about how fidelity is maintained in hosts with 21 multiple co-occurring symbionts. -
Annelids in Extreme Aquatic Environments: Diversity, Adaptations and Evolution
diversity Review Annelids in Extreme Aquatic Environments: Diversity, Adaptations and Evolution Christopher J. Glasby 1,2,*, Christer Erséus 3 and Patrick Martin 4 1 Natural Sciences, Museum & Art Gallery Northern Territory, PO Box 4646, Darwin, NT 0801, Australia 2 Research Institute for the Environment and Livelihoods, Charles Darwin University, Casuarina, NT 0810, Australia 3 Systematics and Biodiversity, Department of Biological and Environmental Sciences, University of Gothenburg, Box 463, SE-405 30 Göteborg, Sweden; [email protected] 4 Royal Belgian Institute of Natural Sciences, Taxonomy and Phylogeny, 29 rue Vautier, B-1000 Brussels, Belgium; [email protected] * Correspondence: [email protected] Abstract: We review the variety of morphological, physiological and behavioral modifications that annelids have acquired to cope with environments either unsuitable for, or on the limits of, survival for most animals. We focus on polychaetes (excluding sipunculans and echiurans) and clitellates (oligochaetes and leeches) and source information mostly from the primary literature. We identified many modifications common to both polychaetes and clitellates, and others that are specific to one or the other group. For example, certain land-adapted polychaetes show reduction in nuchal organs, epidermal ciliation and receptor cells, and other coastal polychaetes use adhesive glands and glue-reinforced tubes to maintain position in surf zones, while oligochaetes, with their simple body plans, appear to be ‘pre-adapted’ to life underground. Modifications common to both groups include the ability to construct protective cocoons, make cryoprotective substances such as Citation: Glasby, C.J.; Erséus, C.; antifreeze and heat shock proteins, develop gills, transform their bodies into a home for symbiotic Martin, P. -
Download Full Report 1.7MB .Pdf File
Museum Victoria Science Reports 13: 1–26 (2010) ISSN 0 7311-7253 1 (Print) 0 7311-7260 4 (On-line) https://doi.org/10.24199/j.mvsr.2010.13 Tools for identifying selected Australian aquatic oligochaetes (Clitellata: Annelida) ADRIAN PINDER Science Division, Department of Environment and Conservation, P.O. Box 51, Wanneroo, 6946, Western Australia; [email protected] Abstract Pinder, A. 2010. Tools for identifying selected Australian aquatic oligochaetes (Clitellata: Annelida). Museum Victoria Science Reports 13: 1-26. Since Pinder and Brinkhurst (1994) produced a „preliminary‟ guide to identifying Australian limnic oligochaetes there have been numerous new species described and substantial insights made into oligochaete phylogenetics, the latter reflected in recent changes to oligochaete classification. This report updates Pinder and Brinkhurst (1994) by 1) updating the taxonomy, 2) better describing and illustrating the characters and methods required to identify aquatic oligochaetes and 3) providing keys to the major groups of marine and freshwater aquatic oligochaetes (and some allied worms) and of all species of the subfamily Naidinae known from Australia. The impetus for this report was a workshop on aquatic invertebrate identification organised by La Trobe University and the Taxonomic Research and Information Network (TRIN). Keywords Aquatic Oligochaeta, Clitellata, identification, Australia, Naididae, Naidinae Introduction 2002; Erséus et al., 2005; IUZN, 2007). Thus the former Naididae s.s. is now a subfamily, Naidinae, within a larger The oligochaete fauna of Australian Inland waters was Naididae that also includes the former tubificid subfamilies reviewed in the identification guide of Pinder and Brinkhurst (Tubificinae, Rhyacodrilinae, Phallodrilinae, (1994). Since that that publication there have been significant Limnodriloidinae and Telmatodrilinae). -
Olavius Algarvensis Juliane Wippler1,6*† , Manuel Kleiner1,2*†, Christian Lott1,3, Alexander Gruhl1, Paul E
Wippler et al. BMC Genomics (2016) 17:942 DOI 10.1186/s12864-016-3293-y RESEARCHARTICLE Open Access Transcriptomic and proteomic insights into innate immunity and adaptations to a symbiotic lifestyle in the gutless marine worm Olavius algarvensis Juliane Wippler1,6*† , Manuel Kleiner1,2*†, Christian Lott1,3, Alexander Gruhl1, Paul E. Abraham4, Richard J. Giannone4, Jacque C. Young4,5, Robert L. Hettich4 and Nicole Dubilier1 Abstract Background: The gutless marine worm Olavius algarvensis has a completely reduced digestive and excretory system, and lives in an obligate nutritional symbiosis with bacterial symbionts. While considerable knowledge has been gained of the symbionts, the host has remained largely unstudied. Here, we generated transcriptomes and proteomes of O. algarvensis to better understand how this annelid worm gains nutrition from its symbionts, how it adapted physiologically to a symbiotic lifestyle, and how its innate immune system recognizes and responds to its symbiotic microbiota. Results: Key adaptations to the symbiosis include (i) the expression of gut-specific digestive enzymes despite the absence of a gut, most likely for the digestion of symbionts in the host's epidermal cells; (ii) a modified hemoglobin that may bind hydrogen sulfide produced by two of the worm’s symbionts; and (iii) the expression of a very abundant protein for oxygen storage, hemerythrin, that could provide oxygen to the symbionts and the host under anoxic conditions. Additionally, we identified a large repertoire of proteins involved in interactions between the worm's innate immune system and its symbiotic microbiota, such as peptidoglycan recognition proteins, lectins, fibrinogen-related proteins, Toll and scavenger receptors, and antimicrobial proteins. -
A Comparison of Intertidal Metazoan Biodiversity Between Previously
Louisiana State University LSU Digital Commons LSU Master's Theses Graduate School March 2021 A Comparison of Intertidal Metazoan Biodiversity Between Previously Oiled Sheared and Intact Marsh Margins and Between Multiple Salinity Zones in the Coastal Marshes of Louisiana Patrick M. Rayle Louisiana State University and Agricultural and Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_theses Part of the Biodiversity Commons, Bioinformatics Commons, Biology Commons, Environmental Microbiology and Microbial Ecology Commons, and the Molecular Biology Commons Recommended Citation Rayle, Patrick M., "A Comparison of Intertidal Metazoan Biodiversity Between Previously Oiled Sheared and Intact Marsh Margins and Between Multiple Salinity Zones in the Coastal Marshes of Louisiana" (2021). LSU Master's Theses. 5287. https://digitalcommons.lsu.edu/gradschool_theses/5287 This Thesis is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Master's Theses by an authorized graduate school editor of LSU Digital Commons. For more information, please contact [email protected]. A COMPARISON OF INTERTIDAL METAZOAN BIODIVERSITY BETWEEN PREVIOUSLY OILED SHEARED AND INTACT MARSH MARGINS AND BETWEEN MULTIPLE SALINITY ZONES IN THE COASTAL MARSHES OF LOUISIANA A Thesis Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfilment of the requirements for the degree of Master of Science in The Department of Entomology by Patrick Michael Rayle B.S., Louisiana State University, 2015 May 2021 Acknowledgements This research was made possible through grants from the Gulf of Mexico Research Initiative. I would like to extend my thanks to Dr. -
Microbial Symbiosis in Annelida
Symbiosis, 38 (2005) 1--45 1 Balaban, Philadelphia/Rehovot Review article Microbial Symbiosis in Annelida MONIKA BRIGHTl * and OLAV GIERE2 1Jnstitute of Ecology and Conservation Biology, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria, Tel. +43-14277-54331, Fax. +43-142 77-54339, Email. [email protected]; 2zoologisches Institut und Zoologisches Museum, Universitiit Hamburg, Martin-Luther-King-Platz 3, D-20149 Hamburg, Germany, Tel. +49-42838-3865, Fax. +49-42838-3937, Email. [email protected] Received March 4, 2004; Accepted June 3, 2004 Abstract Among Annelida various taxa have independently established symbioses with numerous phylotypes of bacteria, the most renowned symbiosis being that of the giant tube worms around hydrothermal vents. Taxonomically, the symbiotic associations range on the host side from a few genera within else aposymbiotic groups (Tubificidae in the Oligochaeta or Glossiphoniidae in the Hirudinea) to higher taxa with all their species living in symbiosis (Siboglinidae, Alvinellidae in the "Polychaeta"). The ties between partners range from rather loose and occasional associations (some mud-dwelling tubificids) over regular ectosyrnbiosis (Alvinellids) to obligatory extra- or intracellular incorporation into the body (gutless oligochaetes, glossiphoniid leeches, siboglinid tube worms). Occurring from eulittoral beaches to deep-sea hot vents, from rotting wood at the sea bottom to freshwater ponds, the associations with bacteria seem to have adaptive significance in a broad ecological and nutritional range. In the sea, chemoautotrophy in sulfidic, otherwise hostile environments is a major factor driving the symbioses, but trophic specializations such as digestion of wood or blood also seem to favor a coordinated and mutually beneficial association with bacteria. -
Australian Biological Resources Study Australian Faunal Directory
12/21/2017 Australian Faunal Directory Australian Biological Resources Study Australian Faunal Directory Y ou are here: Environment home » Biodiversity » A BRS » A FD » C hecklist » Kingdom ANIMALIA Phylum ACANTHOCEPHALA Koelreuther, 1771 Phylum PORIFERA Grant, 1836 Phylum TARDIGRADA Phylum CNIDARIA Phylum CTENOPHORA Eschscholtz, 1829 Phylum DICYEMIDA Van Beneden, 1876 Phylum PLATYHELMINTHES Minot, 1876 Phylum XENACOELOMORPHA Philippe, Brinkmann, Copley, Moroz, Nakano, Poustka, Wallberg, Peterson & Telford, 2011 Phylum NEMERTEA Phylum GASTROTRICHA Phylum ROTIFERA Phylum CHAETOGNATHA Phylum KINORHYNCHA Phylum GNATHOSTOMULIDA Phylum LORICIFERA Kristensen, 1983 Phylum NEMATODA Phylum NEMATOMORPHA Phylum BRYOZOA Ehrenberg, 1831 Phylum BRACHIOPODA Phylum MOLLUSCA Phylum PHORONIDA Hatschek, 1888 Phylum PRIAPULIDA Phylum SIPUNCULA Phylum ECHIURA Phylum KAMPTOZOA Phylum ANNELIDA Class POLYCHAETA Claparède, 1864 Class POGONOPHORA Superclass CLITELLATA Class OLIGOCHAETA Subclass CRASSICLITELLATA Jamieson, 1988 Family OCNERODRILIDAE Eukerria Michaelsen, 1935 Eukerria kuekenthali (Michaelsen, 1908) Eukerria saltensis (Beddard, 1895) Gordiodrilus Beddard, 1892 Gordiodrilus elegans Beddard, 1892 Ocnerodrilus Eisen, 1878 Ocnerodrilus occidentalis Eisen, 1878 Family EUDRILIDAE Eudrilus Perrier, 1871 Eudrilus eugeniae (Kinberg, 1867) Family GLOSSOSCOLECIDAE Pontoscolex Schmarda, 1861 Pontoscolex corethrurus (Müller, 1857) Family LUMBRICIDAE Allolobophora Eisen, 1873 Allolobophora chlorotica (Savigny in Cuvier, 1826) Allolobophora chlorotica chlorotica