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Rotifera: Monogononta) from Minorcan Inland Waters (Balearic Isles: Spain
CONTRIBUTION TO THE KNOWLEDGE OF THE ROTIFER FAUNA (ROTIFERA: MONOGONONTA) FROM MINORCAN INLAND WATERS (BALEARIC ISLES: SPAIN) J. De Manuel Departament d'Ecologia, Facultat de Biologia, Universitat de Barcelona. Avda. Diagonal 645, 08028 Barcelona. Spain. Keywords: Rotifera, new records, Baleanc, archipelago, biogeography, Spain. ABSTRACT Forty-four species of rotifers have been identified in Minorca inland waters. Permanent ponds, temporary pools, flowing waters, and artificial pools were sampled. Most of the species are new records for the island and twenty- nine are new to the Balearic Isles. The families Brachionidae and Lecanidae provide half of the taxa. Keratella procurva (Thorpe, 1912), which is considered a subtropical species, occurred with a widespread distnbution in the island. Different taxa and «Formenkreis» found are mentioned. Original drawings and scanning photomicrographs of some species are presented. Typical assemblages of populations from every environment are also described. INTRODUCTION ficult if we are focusing on the rotifer commu- nities. Traditionally, rotifers have been considered as Rotifers from the Balearic Isles have been in- cosmopolitan organisms of scanty biogeographical sufficiently studied, the only records are from the interest. However, an important degree of ende- works on freshwater biology by MARGALEF (1951, micity has been obsewed in species found in iso- 1952, 1953), DE RIDDER (1967), and PRETUS lated areas from severa1 latitudes (DUMONT,1983). (1989). It suggests that the zoogeographical significance The present paper adds new records to the of rotifers cannot be undewalued. knowledge of the rotifer fauna of Minorca. It in- Production of resting eggs, which may be vestigates the occurrence of the species in the dif- carried by air or accidentally by migrating birds, ferent habitat categories sampled, and discusses as well as by «human transport~,is an efficient some biogeographical particularities. -
The Taxonomy of Brachionus Plicatilis Species Complex (Rotifera: Monogononta) from the Southern Kerala (India) with a Note on Their Repro- Ductive Preferences
J. Mar. Biol. Ass. India, 48 (I) : 6 - 13, January - June 2006 The taxonomy of Brachionus plicatilis species complex (Rotifera: Monogononta) from the Southern Kerala (India) with a note on their repro- ductive preferences P. S Anitha and Rani Mary George Central Marine Fisheries Research Institute, P. B. No. 1603, Ernakulam North P. O., Cochin-682 018, India E. mail: [email protected] Abstract This paper deals with the species of Brackionu.s plicatilis complex (Rotifera: Monogononta) found in a brackishwater lake,Veli-Aakulam, in Southern Kerala. Morphological and reproductive potential studies revealed that these rotifers have sigiificant morphological distinction with regard to ecological preferences. The three related rotifers in our study were classified as Brachionu.~plicatilis Miiller, 1786, B. rotundifi)rmi.s Tschugunoff, 1921 and B. murrayi Fadeew, 1925. The fine morphology and morphometric data revealed that taxonomic characters were constant enough to recognize three well-defined morphologies and B. rrlurrayi is redescribed. The reproductive potential studies in relation to ecological parameters showed that the 'r' values of these rotifers were significantly influenced by salinity as well as temperature, and was species specific. In the light of reproductive preferences, the reorganization of three distinct species has been confirmed by this study and this would allow further comparative work in these lines on this economically important species complex. Keywords: Brachionus plicatilis species complex, reproductive preferences Introduction Among brachionid rotifers, Brachionus plicatilis The occurrence of B. plicatilis in Indian waters was Miiller, 1786 (Monogononta) is probably one of the best- noted by a few numbers of workers (Rao and Mohan, studied taxa because of its suitability as an initial live feed 1984; Shakuntala and Singh, 1993; Gopakumar and for various finfish and shellfish larvae (Lubzens, 1987). -
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. -
Antarctic Bdelloid Rotifers: Diversity, Endemism and Evolution
1 Antarctic bdelloid rotifers: diversity, endemism and evolution 2 3 Introduction 4 5 Antarctica’s ecosystems are characterized by the challenges of extreme environmental 6 stresses, including low temperatures, desiccation and high levels of solar radiation, all of 7 which have led to the evolution and expression of well-developed stress tolerance features in 8 the native terrestrial biota (Convey, 1996; Peck et al., 2006). The availability of liquid water, 9 and its predictability, is considered to be the most important driver of biological and 10 biodiversity processes in the terrestrial environments of Antarctica (Block et al., 2009; 11 Convey et al., 2014). Antarctica’s extreme conditions and isolation combined with the over- 12 running of many, but importantly not all, terrestrial and freshwater habitats by ice during 13 glacial cycles, underlie the low overall levels of diversity that characterize the contemporary 14 faunal, floral and microbial communities of the continent (Convey, 2013). Nevertheless, in 15 recent years it has become increasingly clear that these communities contain many, if not a 16 majority, of species that have survived multiple glacial cycles over many millions of years 17 and undergone evolutionary radiation on the continent itself rather than recolonizing from 18 extra-continental refugia (Convey & Stevens, 2007; Convey et al., 2008; Fraser et al., 2014). 19 With this background, high levels of endemism characterize the majority of groups that 20 dominate the Antarctic terrestrial fauna, including in particular Acari, Collembola, Nematoda 21 and Tardigrada (Pugh & Convey, 2008; Convey et al., 2012). 22 The continent of Antarctica is ice-bound, and surrounded and isolated from the other 23 Southern Hemisphere landmasses by the vastness of the Southern Ocean. -
Investigation of a Rotifer (Brachionus Calyciflorus) - Green Alga (Scenedesmus Pectinatus) Interaction Under Non- and Nutrient-Limi- Ted Conditions
Ann. Limnol. - Int. J. Lim. 2006, 42 (1), 9-17 Investigation of a rotifer (Brachionus calyciflorus) - green alga (Scenedesmus pectinatus) interaction under non- and nutrient-limi- ted conditions M. Lürling Aquatic Ecology & Water Quality Management, Department of Environmental Sciences, Wageningen University, PO Box 8080, NL-6700DD Wageningen, The Netherlands Two-day life cycle tests with the rotifer Brachionus calyciflorus were run to study the nutritional quality effects to rotifers of Scenedesmus pectinatus grown under non-limiting, nitrogen limiting and phosphorus limiting conditions and the feedback of the rotifers on the food algae. Under nutrient-limited conditions of its algal food Brachionus production was depressed, animals pro- duced fewer eggs and were smaller sized. Clearance rates of Brachionus offered non-nutrient-limited and nutrient-limited food were similar. The number of cells per colony was similar for S. pectinatus under nitrogen limited and phosphorus limited condi- tions both in the absence and presence of Brachionus. Cell volumes of phosphorus limited S. pectinatus were larger than those of nitrogen limited cells. The most dramatic response of the food alga S. pectinatus was observed in non-nutrient-limited condi- tions: a strong size enlargement occurred only in the presence of Brachionus. This was caused by a higher share of eight-celled colonies and larger individual cell volumes in the presence of rotifers than in their absence. S. pectinatus might gain an advan- tage of becoming larger in moving out of the feeding window of its enemy, but nutrient limited conditions might undermine the effectiveness of such reaction. Keywords : clearance rate, food quality, grazing, induced defence, morphology, plankton interactions Introduction constraints on growth, but also food quality constraints. -
A Data Set on the Distribution of Rotifera in Antarctica
Biogeographia – The Journal of Integrative Biogeography 35 (2020): 17-25 https://doi.org/10.21426/B635044786 A data set on the distribution of Rotifera in Antarctica GIUSEPPE GARLASCHÈ1, KARIMULLAH KARIMULLAH1,2, NATALIIA IAKOVENKO3,4,5, ALEJANDRO VELASCO-CASTRILLÓN6, KAREL JANKO4,5, ROBERTO GUIDETTI7, LORENA REBECCHI7, MATTEO CECCHETTO8,9, STEFANO SCHIAPARELLI8,9, CHRISTIAN D. JERSABEK10, WILLEM H. DE SMET11, DIEGO FONTANETO1,* 1 National Research Council of Italy, Water Research Institute (CNR-IRSA), Verbania Pallanza (Italy) 2 University of Leipzig, Faculty of Life Science, Institute of Biology, Behavioral Ecology Research Group, Leipzig (Germany) 3 University of Life Sciences in Prague, Praha-Suchdol (Czech Republic) 4 Department of Biology and Ecology, Faculty of Science, University of Ostrava, Ostrava (Czech Republic) 5 Laboratory of Fish Genetics, Institute of Animal Physiology and Genetics AS CR, Liběchov (Czech Republic) 6 South Australian Museum, Adelaide, (Australia) 7 Department of Life Science, University of Modena and Reggio Emilia, Modena (Italy) 8 Department of Earth, Environmental and Life Science (DISTAV), University of Genoa, Genoa (Italy) 9 Italian National Antarctic Museum (MNA, Section of Genoa), University of Genoa, Genoa (Italy) 10 Division of Animal Structure and Function, University of Salzburg, Salzburg (Austria) 11 Department of Biology, ECOBE, University of Antwerp Campus Drie Eiken, Wilrijk (Belgium) * email corresponding author: [email protected] Keywords: ANTABIF, Antarctica, Bdelloidea, biodiversity, biogeography, GBIF, Monogononta, rotifers. SUMMARY We present a data set on Antarctic biodiversity for the phylum Rotifera, making it publicly available through the Antarctic Biodiversity Information facility. We provide taxonomic information, geographic distribution, location, and habitat for each record. The data set gathers all the published literature about rotifers found and identified across the Continental, Maritime, and Subantarctic biogeographic regions of Antarctica. -
The Global Invertebrate Genomics Alliance
Journal of Heredity 2014:105(1):1–18 © The American Genetic Association 2013. All rights reserved. doi:10.1093/jhered/est084 For permissions, please e-mail: [email protected] The Global Invertebrate Genomics Alliance (GIGA): Developing Community Resources to Study Downloaded from https://academic.oup.com/jhered/article-abstract/105/1/1/858593 by University of Florida, Joseph Ryan on 28 May 2019 Diverse Invertebrate Genomes GIGA COMMUNiTY OF SciENTisTs* Address correspondence to Dr. Jose V. Lopez, Oceanographic Center, Nova Southeastern University, 8000 North Ocean Drive, Dania Beach, FL 33004, or e-mail: [email protected]. *Authors are listed in the Appendix Abstract Over 95% of all metazoan (animal) species comprise the “invertebrates,” but very few genomes from these organisms have been sequenced. We have, therefore, formed a “Global Invertebrate Genomics Alliance” (GIGA). Our intent is to build a collaborative network of diverse scientists to tackle major challenges (e.g., species selection, sample collection and storage, sequence assembly, annotation, analytical tools) associated with genome/transcriptome sequencing across a large taxonomic spectrum. We aim to promote standards that will facilitate comparative approaches to invertebrate genomics and collabora- tions across the international scientific community. Candidate study taxa include species from Porifera, Ctenophora, Cnidaria, Placozoa, Mollusca, Arthropoda, Echinodermata, Annelida, Bryozoa, and Platyhelminthes, among others. GIGA will target 7000 noninsect/nonnematode species, with an emphasis on marine taxa because of the unrivaled phyletic diversity in the oceans. Priorities for selecting invertebrates for sequencing will include, but are not restricted to, their phylogenetic placement; relevance to organismal, ecological, and conservation research; and their importance to fisheries and human health. -
Diplomarbeit
DIPLOMARBEIT Titel der Diplomarbeit Zooplankton dynamics of two alkaline-saline lakes in the Kenyan Rift Valley Angestrebter akademischer Grad: Magister der Naturwissenschaften (Mag. rer. nat.) Verfasser: Alfred Burian Studienrichtung: Zoologie Betreuer: Prof. Michael Schagerl - 1 - Population of Lesser Flamingo at the shores of Lake Bogoria. - 2 - Table of content 1. Introduction to the ecology of East African salt lakes (German).......................................- 4 - 3. Feeding behaviour of dominant zooplankton grazers and their influence on phytoplankton and the microbial loop in saline-alkaline Kenyan Rift Valley Lakes....................................... 36 4. Zooplankton dynamics of tropical saline lakes: an analysis of rotifer biomass outbursts. .. 64 5. English summary.................................................................................................................. 91 6. Deutsche Kurzzusammenfassung......................................................................................... 93 7. Acknowledgements:............................................................................................................. 95 8. Curriculum Vitae: Alfred Burian ......................................................................................... 96 - 3 - 1. Introduction to the ecology of East African salt lakes (German) Die Salzseen des ostafrikanischen Grabenbruchs sind nicht nur durch ihre atemberaubende Landschaft einzigartig, sondern heben sich auch durch eine Reihe von Umwelt- und biologischen Faktoren -
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ISSN 0974-7907 (Online) OPEN ACCESS ISSN 0974-7893 (Print) 26 October 2018 (Online & Print) Vol. 10 | No. 11 | 12443–12618 10.11609/jot.2018.10.11.12443-12618 www.threatenedtaxa.org Building evidence for conservatonJ globally TTJournal of Threatened Taxa YOU DO ... ... BUT I DON’T SEE THE DIFFERENCE. ISSN 0974-7907 (Online); ISSN 0974-7893 (Print) Published by Typeset and printed at Wildlife Informaton Liaison Development Society Zoo Outreach Organizaton No. 12, Thiruvannamalai Nagar, Saravanampat - Kalapat Road, Saravanampat, Coimbatore, Tamil Nadu 641035, India Ph: 0 938 533 9863 Email: [email protected], [email protected] www.threatenedtaxa.org EDITORS Christoph Kuefer, Insttute of Integratve Biology, Zürich, Switzerland Founder & Chief Editor Christoph Schwitzer, University of the West of England, Clifon, Bristol, BS8 3HA Dr. Sanjay Molur, Coimbatore, India Christopher L. Jenkins, The Orianne Society, Athens, Georgia Cleofas Cervancia, Univ. of Philippines Los Baños College Laguna, Philippines Managing Editor Colin Groves, Australian Natonal University, Canberra, Australia Mr. B. Ravichandran, Coimbatore, India Crawford Prentce, Nature Management Services, Jalan, Malaysia C.T. Achuthankuty, Scientst-G (Retd.), CSIR-Natonal Insttute of Oceanography, Goa Associate Editors Dan Challender, University of Kent, Canterbury, UK Dr. B.A. Daniel, Coimbatore, India D.B. Bastawade, Maharashtra, India Dr. Ulrike Streicher, Wildlife Veterinarian, Danang, Vietnam D.J. Bhat, Retd. Professor, Goa University, Goa, India Ms. Priyanka Iyer, Coimbatore, India Dale R. Calder, Royal Ontaro Museum, Toronto, Ontario, Canada Dr. Manju Siliwal, Dehra Dun, India Daniel Brito, Federal University of Goiás, Goiânia, Brazil Dr. Meena Venkataraman, Mumbai, India David Mallon, Manchester Metropolitan University, Derbyshire, UK David Olson, Zoological Society of London, UK Editorial Advisors Davor Zanella, University of Zagreb, Zagreb, Croata Ms. -
Key to the Identification of the Genera of Bdelloid Rotifers
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/225970221 Key to the identification of the genera of Bdelloid Rotifers Article in Hydrobiologia · January 2000 DOI: 10.1023/A:1003840216827 CITATIONS READS 55 894 2 authors: Claudia Ricci Giulio Melone University of Milan University of Milan 133 PUBLICATIONS 3,320 CITATIONS 101 PUBLICATIONS 1,905 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Fauna Europaea View project I enjoy my retirement View project All content following this page was uploaded by Giulio Melone on 03 April 2015. The user has requested enhancement of the downloaded file. Hydrobiologia 418: 73–80, 2000. 73 © 2000 Kluwer Academic Publishers. Printed in the Netherlands. Key to the identification of the genera of bdelloid rotifers Claudia Ricci & Giulio Melone Department of Biology, Milan University, Milan, Italy Fax: [+39]-(0)2-236-2726. E-mail: [email protected] Received 6 April 1999; in revised form 29 July 1999; accepted 19 August 1999 Key words: Rotifera, Bdelloidea, pictorial key, taxonomy Abstract We propose a simple, user-friendly key joined to a pictorial key to the bdelloid genera, in the attempt to make bdelloid identification more accessible to non-bdelloid-specialists. The key is mostly based on illustrations rather than on descriptions, and is accompanied by an introduction of the main features readily observable in active bdelloids. Introduction (e.g. Ward et al., 1998). Most studies recording the taxonomic composition of freshwater microinverteb- Bdelloids constitute a class of the phylum Rotifera, rate assemblages disregard the bdelloid communities distinguished by two characteristics that are autoapo- and provide total counts of the bdelloid specimens morphic to the whole class: (1) obligatory partheno- only, without discriminating lower taxon categories genetic reproduction (Gilbert, 1983), and (2) ability to (i.e. -
Temperature-Dependent Life History and Transcriptomic
Temperature-dependent life history and transcriptomic responses in heat-tolerant versus heat-sensitive Brachionus rotifers Sofia Paraskevopoulou1, Alice Dennis1, Guntram Weithoff1, and Ralph Tiedemann1 1University of Potsdam May 5, 2020 Abstract A species’ response to thermal stress is an essential physiological trait that can determine occurrence and temporal succession in nature, including response to climate change. Environmental temperature affects zooplankton performance by altering life-spans and population growth rates, but the molecular mechanisms underlying these alterations are largely unknown. To compare temperature-related demography, we performed cross-temperature life-table experiments in closely related heat-tolerant and heat-sensitive Brachionus rotifer species that occur in sympatry. Within these same populations, we examined the genetic basis of physiological variation by comparing gene expression across increasing temperatures. We found significant cross-species and cross-temperature differences in heat response, with the heat-sensitive species adopting a strategy of high survival and low population growth, while the heat-tolerant followed an opposite strategy. Comparative transcriptomic analyses revealed both shared and opposing responses to heat. Most notably, expression of heat shock proteins (hsps) is strikingly different in the two species. In both species, hsp responses mirrored differences in population growth rates, showing that hsp genes are likely a key component of a species’ adaptation to different temperatures. Temperature induction caused opposing patterns of expression in further functional categories such as energy, carbohydrate and lipid metabolism, and in genes related to ribosomal proteins. In the heat-sensitive species, elevated temperatures caused up-regulation of genes related to induction of meiotic division as well as genes responsible for post-translational histone modifications. -
Evolution of Reproduction and Stress Tolerance In
EVOLUTION OF REPRODUCTION AND STRESS TOLERANCE IN BRACHIONID ROTIFERS A Dissertation Presented to The Academic Faculty by Hilary April Smith In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the School of Biology Georgia Institute of Technology August 2012 EVOLUTION OF REPRODUCTION AND STRESS TOLERANCE IN BRACHIONID ROTIFERS Approved by: Dr. Terry W. Snell, Advisor Dr. J. Todd Streelman School of Biology School of Biology Georgia Institute of Technology Georgia Institute of Technology Dr. Mark E. Hay Dr. David B. Mark Welch School of Biology Josephine Bay Paul Center for Georgia Institute of Technology Comparative Molecular Biology and Evolution Marine Biological Laboratory Dr. Julia Kubanek Dr. Robert L. Wallace School of Biology Department of Biology Georgia Institute of Technology Ripon College Date Approved: April 30, 2012 To Ginny and Dale Smith. ACKNOWLEDGEMENTS I wish to acknowledge all those who have contributed to the production of this dissertation directly or indirectly. First, I thank my parents for their support. Second, I express gratitude to my doctoral advisor Dr. Snell, without whom this would not have been possible. I also thank members past and present of the Snell laboratory, including but not limited to Dr. Shearer, Allison Fields, Ashleigh Burns, and Kathleen White. Third, I would like to thank my committee members, Dr. Hay, Dr. Kubanek, Dr. Streelman, Dr. Mark Welch, and Dr. Wallace, for their guidance and assistance. Fourth, I acknowledge Dr. Serra and Dr. Carmona, and members of their laboratories, for hosting me at the University of Valencia and providing aid with sampling and culture work in Spain.