International Conference on Rotifers Illmitz
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Paper Received: 28.11.2019 Revised Received: 11.12.2019 Accepted: 12.12.2019
Journal Home page : www.jeb.co.in « E-mail : [email protected] Review Article Journal of Environmental Biology TM p-ISSN: 0254-8704 e-ISSN: 2394-0379 JEB CODEN: JEBIDP DOI : http://doi.org/10.22438/jeb/41/1/MRN-1344 White Smoke Plagiarism Detector Just write. Review on the ecology and taxonomy of sessile rotifers (Rotifera) with special reference to Mexico S.S.S. Sarma1*, M.A. Jiménez-Santos2, S. Nandini1 and R.L. Wallace3 1Laboratory of Aquatic Zoology, National Autonomous University of Mexico, CP-54090 Tlalnepantla, México 2Posgrado en Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, CP-04510, Mexico 3Department of Biology, Ripon College, Ripon, WI 54971-0248, USA *Corresponding Author Email : [email protected] Paper received: 28.11.2019 Revised received: 11.12.2019 Accepted: 12.12.2019 Abstract Although comprising <0.5% of all the known species of Rotifera, sessile rotifers are an important component in freshwater ecosystems, especially shallow waterbodies. During the last eight decades, fewer than 80 publications have dealt specifically with sessile rotifers, while more than 7600 articles have focused on rotifers in general. In this work research on the sessile rotifers with emphasis on the Mexican fauna has been reviewed and some additional information on the new records has been included. Difficulties involved in collection and maintenance of sessile rotifers, as well as problems of identification and quantification have been considered. Published data on the ecology and taxonomy of this group has also been reviewed. There are 35 species of sessile rotifers from three families Atrochidae, Collothecidae, and Flosculariidae, but to that four more species in the planktonic family Conochilidae may be added, as recent molecular research indicates that this family lies within Flosculariidae. -
Number of Living Species in Australia and the World
Numbers of Living Species in Australia and the World 2nd edition Arthur D. Chapman Australian Biodiversity Information Services australia’s nature Toowoomba, Australia there is more still to be discovered… Report for the Australian Biological Resources Study Canberra, Australia September 2009 CONTENTS Foreword 1 Insecta (insects) 23 Plants 43 Viruses 59 Arachnida Magnoliophyta (flowering plants) 43 Protoctista (mainly Introduction 2 (spiders, scorpions, etc) 26 Gymnosperms (Coniferophyta, Protozoa—others included Executive Summary 6 Pycnogonida (sea spiders) 28 Cycadophyta, Gnetophyta under fungi, algae, Myriapoda and Ginkgophyta) 45 Chromista, etc) 60 Detailed discussion by Group 12 (millipedes, centipedes) 29 Ferns and Allies 46 Chordates 13 Acknowledgements 63 Crustacea (crabs, lobsters, etc) 31 Bryophyta Mammalia (mammals) 13 Onychophora (velvet worms) 32 (mosses, liverworts, hornworts) 47 References 66 Aves (birds) 14 Hexapoda (proturans, springtails) 33 Plant Algae (including green Reptilia (reptiles) 15 Mollusca (molluscs, shellfish) 34 algae, red algae, glaucophytes) 49 Amphibia (frogs, etc) 16 Annelida (segmented worms) 35 Fungi 51 Pisces (fishes including Nematoda Fungi (excluding taxa Chondrichthyes and (nematodes, roundworms) 36 treated under Chromista Osteichthyes) 17 and Protoctista) 51 Acanthocephala Agnatha (hagfish, (thorny-headed worms) 37 Lichen-forming fungi 53 lampreys, slime eels) 18 Platyhelminthes (flat worms) 38 Others 54 Cephalochordata (lancelets) 19 Cnidaria (jellyfish, Prokaryota (Bacteria Tunicata or Urochordata sea anenomes, corals) 39 [Monera] of previous report) 54 (sea squirts, doliolids, salps) 20 Porifera (sponges) 40 Cyanophyta (Cyanobacteria) 55 Invertebrates 21 Other Invertebrates 41 Chromista (including some Hemichordata (hemichordates) 21 species previously included Echinodermata (starfish, under either algae or fungi) 56 sea cucumbers, etc) 22 FOREWORD In Australia and around the world, biodiversity is under huge Harnessing core science and knowledge bases, like and growing pressure. -
Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016
Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016 April 1981 Revised, May 1982 2nd revision, April 1983 3rd revision, December 1999 4th revision, May 2011 Prepared for U.S. Department of Commerce Ohio Department of Natural Resources National Oceanic and Atmospheric Administration Division of Wildlife Office of Ocean and Coastal Resource Management 2045 Morse Road, Bldg. G Estuarine Reserves Division Columbus, Ohio 1305 East West Highway 43229-6693 Silver Spring, MD 20910 This management plan has been developed in accordance with NOAA regulations, including all provisions for public involvement. It is consistent with the congressional intent of Section 315 of the Coastal Zone Management Act of 1972, as amended, and the provisions of the Ohio Coastal Management Program. OWC NERR Management Plan, 2011 - 2016 Acknowledgements This management plan was prepared by the staff and Advisory Council of the Old Woman Creek National Estuarine Research Reserve (OWC NERR), in collaboration with the Ohio Department of Natural Resources-Division of Wildlife. Participants in the planning process included: Manager, Frank Lopez; Research Coordinator, Dr. David Klarer; Coastal Training Program Coordinator, Heather Elmer; Education Coordinator, Ann Keefe; Education Specialist Phoebe Van Zoest; and Office Assistant, Gloria Pasterak. Other Reserve staff including Dick Boyer and Marje Bernhardt contributed their expertise to numerous planning meetings. The Reserve is grateful for the input and recommendations provided by members of the Old Woman Creek NERR Advisory Council. The Reserve is appreciative of the review, guidance, and council of Division of Wildlife Executive Administrator Dave Scott and the mapping expertise of Keith Lott and the late Steve Barry. -
Gnesiotrocha, Monogononta, Rotifera) in Thale Noi Lake, Thailand
Zootaxa 2997: 1–18 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Diversity of sessile rotifers (Gnesiotrocha, Monogononta, Rotifera) in Thale Noi Lake, Thailand PHURIPONG MEKSUWAN1, PORNSILP PHOLPUNTHIN1 & HENDRIK SEGERS2,3 1Plankton Research Unit, Department of Biology, Faculty of Science, Prince of Songkla University, Hat Yai 90112, Songkhla, Thai- land. E-mail: [email protected], [email protected] 2Freshwater Laboratory, Royal Belgian Institute of Natural Sciences, Vautierstraat 29, 1000 Brussels, Belgium. E-mail: [email protected] 3Corresponding author Abstract In response to a clear gap in knowledge on the biodiversity of sessile Gnesiotrocha rotifers at both global as well as re- gional Southeast Asian scales, we performed a study of free-living colonial and epiphytic rotifers attached to fifteen aquat- ic plant species in Thale Noi Lake, the first Ramsar site in Thailand. We identified 44 different taxa of sessile rotifers, including thirty-nine fixosessile species and three planktonic colonial species. This corresponds with about 40 % of the global sessile rotifer diversity, and is the highest alpha-diversity of the group ever recorded from a single lake. The record further includes a new genus, Lacinularoides n. gen., containing a single species L. coloniensis (Colledge, 1918) n. comb., which is redescribed, and several possibly new species, one of which, Ptygura thalenoiensis n. spec. is formally described here. Ptygura noodti (Koste, 1972) n. comb. is relocated from Floscularia, based on observations of living specimens of this species, formerly known only from preserved, contracted specimens from the Amazon region. -
Volume 2, Chapter 4-7C: Invertebrates: Rotifer Taxa
Glime, J. M. 2017. Invertebrates: Rotifer Taxa – Monogononta. Chapt. 4-7c. In: Glime, J. M. Bryophyte Ecology. Volume 2. 4-7c-1 Bryological Interaction. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 18 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 4-7c INVERTEBRATES: ROTIFER TAXA – MONOGONONTA TABLE OF CONTENTS Notommatidae ............................................................................................................................................ 4-7c-2 Cephalodella ....................................................................................................................................... 4-7c-2 Drilophaga ........................................................................................................................................ 4-7c-10 Enteroplea ......................................................................................................................................... 4-7c-11 Eosphora ........................................................................................................................................... 4-7c-11 Eothinia ............................................................................................................................................. 4-7c-12 Monommata ...................................................................................................................................... 4-7c-12 Notommata ....................................................................................................................................... -
In Worms Geoff Read NIWA New Zealand
Brussels, 28-30 September Polychaeta (Annelida) in WoRMS Geoff Read NIWA New Zealand www.marinespecies.org/polychaeta/index.php Context interface Swimming — an unexpected skill of Polychaeta Acrocirridae Alciopidae Syllidae Nereididae Teuthidodr ilus = squidworm Acrocirridae Polynoidae Swima bombiviridis Syllidae Total WoRMS Polychaeta records, excluding fossils 91 valid families. Entries >98% editor checked, except Echiura (69%) Group in WoRMS all taxa all species valid species names names names Class Polychaeta 23,872 20,135 11,615 Subclass Echiura 296 234 197 Echiura were recently a Subclass Errantia 12,686 10,849 6,210 separate phylum Subclass Polychaeta incertae sedis 354 265 199 Subclass Sedentaria 10,528 8,787 5,009 Non-marine Polychaeta 28 16 (3 terrestrial) Class Clitellata* 1601 1086 (279 Hirudinea) *Total valid non-leech clitellates~5000 spp, 1700 aquatic. (Martin et al. 2008) Annelida diversity "It is now clear that annelids, in addition to including a large number of species, encompass a much greater disparity of body plans than previously anticipated, including animals that are segmented and unsegmented, with and without parapodia, with and without chaetae, coelomate and acoelomate, with straight guts and with U-shaped digestive tracts, from microscopic to gigantic." (Andrade et al. 2015) Andrade et al (2015) “Articulating “archiannelids”: Phylogenomics and annelid relationships, with emphasis on meiofaunal taxa.” Molecular Biology and Evolution, efirst Myzostomida (images Summers et al)EV Nautilus: Riftia Semenov: Terebellidae Annelida latest phylogeny “… it is now well accepted that Annelida includes many taxa formerly considered different phyla or with supposed affiliations with other animal groups, such as Sipuncula, Echiura, Pogonophora and Vestimentifera, Myzostomida, or Diurodrilida (Struck et al. -
Rotifera: Monogononta)
Anim. Syst. Evol. Divers. Vol. 36, No. 3: 222-227, July 2020 https://doi.org/10.5635/ASED.2020.36.3.046 Review article New Record of Kellicottia bostoniensis and Redescription of Two Freshwater Rotifers from Korea (Rotifera: Monogononta) Hee-Min Yang, Gi-Sik Min* Department of Biological Sciences, Inha University, Incheon 22212, Korea ABSTRACT In this study, we identified three monogonont rotifers from South Korea: Kellicottia bostoniensis (Rousselet, 1908), Trichocerca tenuior (Gosse, 1886), and Lepadella triptera (Ehrenberg, 1830). The distribution records of K. bostoniensis were mainly located in the Nearctic, Neotropic and Western Palearctic regions. After Japan, this is the second record of it in Asia. Trichocerca tenuior and Lepadella triptera have already been recorded in Korea, but the data of two species were insufficient in previous study. Here, we describe the morphological characteristics of the three species and the trophi structures of K. bostoniensis and T. tenuior. This study is the first to characterize the trophi structure of K. bostoniensis, observed using a scanning electron microscope. In addition, we have determined the partial cytochrome c oxidase subunit 1 (COI) and 18S rRNA gene sequences of T. tenuior and L. triptera for their DNA barcodes. Keywords: biodiversity, East Asia, monogonont rotifers, SEM, taxonomy INTRODUCTION 1999). The genus Trichocerca Lamarck, 1801 is a species-rich Research on rotifers in Korea was started by Hada (1936), who taxon in the monogonont rotifers. It comprises 77 species collected 17 species from Lake Seo-ho in Suwon-si, Gyeong- and inhabits various environments such as fresh, brack- gi-do, South Korea. So far, 305 species have been recorded in ish, and marine water (Segers, 2007; Jersabek and Leitner, Korea (National Institute of Biological Resources and Minis- 2013). -
The Biodiverse Rotifers (Rotifera: Eurotatoria)
Bonn zoological Bulletin 68 (1): 147–162 ISSN 2190–7307 2019 · Sharma B.K. & Sharma S. http://www.zoologicalbulletin.de https://doi.org/10.20363/BZB-2019.68.1.147 Research article urn:lsid:zoobank.org:pub:D9308652-B9BF-4BBB-B573-F1C4B53E1AC5 The biodiverse rotifers (Rotifera: Eurotatoria) of Northeast India: faunal heterogeneity, biogeography, richness in diverse ecosystems and interesting species assemblages Bhushan Kumar Sharma1, * & Sumita Sharma2 1, 2 Department of Zoology, North-Eastern Hill University, Shillong – 793 022, Meghalaya, India * Corresponding author: Email: [email protected] 1 urn:lsid:zoobank.org:author:FD069583-6E71-46D6-8F45-90A87F35BEFE 2 urn:lsid:zoobank.org:author:668E0FE0-C474-4D0D-9339-F01ADFD239D1 Abstract. The biodiverse Rotifera of northeast India (NEI) revealed 303 species belonging to 53 genera and 24 families; ~96% of these species examined from seven states of NEI affirm the rotifer heterogeneity of our plankton and semi-plank- ton collections. This study documents the record number of species of global and regional biogeographic interest, high- lights affinity with Southeast Asian and Australian faunas, and indicates notable heterogeneity in richness and composition amongst the seven northeastern states. The speciose rotifers of small lentic biotopes of Arunachal Pradesh, Mizoram, Nagaland, Meghalaya, Manipur and Tripura, the floodplain lakes beels( ) and small wetlands (dobas and dubies) of the Brahmaputra and the Barak floodplains of Assam, and the floodplain lakes (pats) of Manipur are noteworthy. Deepor Beel and Loktak Lake (two Ramsar sites) are the globally rich rotifer `hotspots’. Interesting assemblages per sample of 80+ species in certain beels and pats, and up to 50 species in dobas and dubies depict the `Rotifera paradox’. -
About the Book the Format Acknowledgments
About the Book For more than ten years I have been working on a book on bryophyte ecology and was joined by Heinjo During, who has been very helpful in critiquing multiple versions of the chapters. But as the book progressed, the field of bryophyte ecology progressed faster. No chapter ever seemed to stay finished, hence the decision to publish online. Furthermore, rather than being a textbook, it is evolving into an encyclopedia that would be at least three volumes. Having reached the age when I could retire whenever I wanted to, I no longer needed be so concerned with the publish or perish paradigm. In keeping with the sharing nature of bryologists, and the need to educate the non-bryologists about the nature and role of bryophytes in the ecosystem, it seemed my personal goals could best be accomplished by publishing online. This has several advantages for me. I can choose the format I want, I can include lots of color images, and I can post chapters or parts of chapters as I complete them and update later if I find it important. Throughout the book I have posed questions. I have even attempt to offer hypotheses for many of these. It is my hope that these questions and hypotheses will inspire students of all ages to attempt to answer these. Some are simple and could even be done by elementary school children. Others are suitable for undergraduate projects. And some will take lifelong work or a large team of researchers around the world. Have fun with them! The Format The decision to publish Bryophyte Ecology as an ebook occurred after I had a publisher, and I am sure I have not thought of all the complexities of publishing as I complete things, rather than in the order of the planned organization. -
On the Serotonergic Nervous System of Two Planktonic Rotifers, Conochilus Coenobasis and C
ARTICLE IN PRESS Zoologischer Anzeiger 245 (2006) 53–62 www.elsevier.de/jcz On the serotonergic nervous system of two planktonic rotifers, Conochilus coenobasis and C. dossuarius (Monogononta, Flosculariacea, Conochilidae) Rick Hochbergà Department of Biological Sciences, University of Massachusetts, One University Avenue, Lowell, MA 01854, USA Received 21 November 2005; received in revised form 4 April 2006; accepted 10 April 2006 Corresponding editor: M. Schmitt Abstract The serotonergic nervous systems of two non-colonial species of Conochilus were examined to obtain the first immunohistochemical insights into the neuroanatomy of species of Flosculariacea (Rotifera, Monogononta). Species of Conochilus, subgenus Conochiloides, were examined using serotonin (5-HT) immunohistochemistry, epifluorescence and confocal laser scanning microscopy, and 3D computer imaging software. In specimens of C. coenobasis and C. dossuarius, the serotonergic nervous system is defined by a dorsal cerebral ganglion, apically directed cerebral neurites, and paired nerve cords. The cerebral ganglion contains approximately four pairs of small 5-HT- immunoreactive perikarya; one pair innervates the posterior nerve cords and three pairs innervate the apical field. The most dorsal pair innervates a coronal nerve ring that encircles the apical field. Within the apical field is a second nerve ring that outlines the inner border of the coronal cilia. Together, both the inner and outer nerve rings may function to modulate ciliary activity of the corona. The other two pairs of perikarya innervate a region around the mouth. Specific differences in the distribution of serotonergic neurons between species of Conochilus and previously examined ploimate rotifers include the following: (a) a lack of immunoreactivity in the mastax; (b) a greater number of apically directed serotonergic neurites; and (c) a complete innervation of the corona in both species of Conochilus. -
The Rotifers of Spanish Reservoirs: Ecological, Systematical and Zoogeographical Remarks
91 THE ROTIFERS OF SPANISH RESERVOIRS: ECOLOGICAL, SYSTEMATICAL AND ZOOGEOGRAPHICAL REMARKS Jordi de Manuel Barrabin Departament d'Ecologia, Universitat de Barcelona. Avd. Diagonal 645,08028 Barcelona. Spain,[email protected] ABSTRACT This article covers the rotifer data from a 1987/1988 survey of one hundred Spanish reservoirs. From each species brief infor- mation is given, focused mainly on ecology, morphology, zoogeography and distribution both in Spain and within reservoirs. New autoecological information on each species is also established giving conductivity ranges, alkalinity, pH and temperature for each. Original drawings and photographs obtained on both optical and electronic microscopy are shown of the majority of the species found. In total one hundred and ten taxa were identified, belonging to 101 species, representing 20 families: Epiphanidae (1): Brachionidae (23); Euchlanidae (1); Mytilinidae (1 ): Trichotriidae (3): Colurellidae (8); Lecanidae (1 5); Proalidae (2); Lindiidae (1); Notommatidae (5); Trichocercidae (7); Gastropodidae (5); Synchaetidae (1 1); Asplanchnidae (3); Testudinellidae (3); Conochiliidae (5):Hexarthridae (2); Filiniidae (3); Collothecidae (2); Philodinidae (Bdelloidea) (I). Thirteen species were new records for the Iberian rotifer fauna: Kerutella ticinensis (Ehrenberg); Lepadella (X.) ustucico- la Hauer; Lecane (M.) copeis Harring & Myers; Lecane tenuiseta Harring: Lecane (M.) tethis Harring & Myers; Proales fal- laciosa Wulfert; Lindia annecta Harring & Myers; Notommatu cerberus Hudson & Gosse; Notommata copeus Ehrenberg: Resticula nyssu Harring & Myers; Trichocerca vernalis Hauer; Gustropus hyptopus Ehrenberg: Collothecu mutabilis Hudson. Key Words: Rotifera, plankton, heleoplankton, reservoirs RESUMEN Este urticulo proporciona infiirmacicin sobre 10s rotferos hullados en el estudio 1987/88 realizudo sobre cien embalses espafioles. Para cnda especie se da una breve informacicin, ,fundamentalmente sobre aspectos ecoldgicos, morfoldgicos, zoo- geogriificos, asi como de su distribucidn en EspaAa y en los emldses. -
Bodyplan Diversification in Crinoid-Associated Myzostomes (Myzostomida, Protostomia)
Invertebrate Biology 128(3): 283–301. r 2009, The Authors Journal compilation r 2009, The American Microscopical Society, Inc. DOI: 10.1111/j.1744-7410.2009.00172.x Bodyplan diversification in crinoid-associated myzostomes (Myzostomida, Protostomia) De´borah Lanterbecq,1,a Greg W. Rouse,2 and Igor Eeckhaut1 1 Marine Biology Laboratory, University of Mons-Hainaut, 7000 Mons, Hainaut, Belgium 2 Scripps Institution of Oceanography, University of California, San Diego, La Jolla, California 92093-0202, USA Abstract. When free-living organisms evolve into symbiotic organisms (parasites, commen- sals, or mutualists), their bodyplan is often dramatically modified as a consequence. The present work pertains to the study of this process in a group of marine obligate symbiotic worms, the Myzostomida. These are mainly ectocommensals and are only associated with echinoderms, mostly crinoids. Their usual textbook status as a class of the Annelida is gen- erally accepted, although recent molecular phylogenetic studies have raised doubts on their relationships with other metazoans, and the question of their status remains open. Here, we reconstruct the evolution of their bodyplans by mapping 14 external morphological charac- ters (analyzed using scanning electron microscopy) onto molecular phylogenies using max- imum parsimony (MP) and maximum likelihood (ML) optimality criteria. Rooted MP, ML, and Bayesian phylogenetic trees were obtained by analyzing the nucleotide sequences of cytochrome oxidase subunit I, 18S rDNA, and 16S rDNA genes, separately and