Geographical Spread of the Invasive Species Kellicottia Longispina (Kellicott, 1879) and K
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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). -
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. -
Redalyc.Geographical Spread of the Invasive Species Kellicottia Longispina (Kellicott, 1879) and K. Bostoniensis (Rousselet
Acta Scientiarum. Biological Sciences ISSN: 1679-9283 [email protected] Universidade Estadual de Maringá Brasil de Fátima Bomfim, Francieli; Mantovano, Tatiane; Fatoreto Schwind, Leilane Talita; Palazzo, Fabiana; Costa Bonecker, Claudia; Lansac-Tôha, Fábio Amodê Geographical spread of the invasive species Kellicottia longispina (Kellicott, 1879) and K. bostoniensis (Rousselet, 1908): A scientometric approach Acta Scientiarum. Biological Sciences, vol. 38, núm. 1, enero-marzo, 2016, pp. 29-36 Universidade Estadual de Maringá Maringá, Brasil Available in: http://www.redalyc.org/articulo.oa?id=187146621005 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Acta Scientiarum http://www.uem.br/acta ISSN printed: 1679-9283 ISSN on-line: 1807-863X Doi: 10.4025/actascibiolsci.v38i1.28252 Geographical spread of the invasive species Kellicottia longispina (Kellicott, 1879) and K. bostoniensis (Rousselet, 1908): A scientometric approach Francieli de Fátima Bomfim*, Tatiane Mantovano, Leilane Talita Fatoreto Schwind, Fabiana Palazzo, Claudia Costa Bonecker and Fábio Amodêo Lansac-Tôha Programa de Pós-graduação em Ecologia de Ambientes Aquáticos Continentais, Núcleo de Pesquisa em Limnologia, Ictiologia e Aquicultura, Laboratório de Zooplâncton, Universidade Estadual de Maringá, Av. Colombo, 5790, 87020-900, Maringá, Paraná, Brazil. *Author for correspondence. E-mail: [email protected] ABSTRACT. Processes related to biological invasion of inland waters have become a major issue due to the increasing number of cases associated with the potential effects of invasions. Kellicottia bostoniensis and K. longispina are rotifer species originating from North America and have become invasive in several continents. -
Population Structuring in the Monogonont Rotifer Synchaeta Pectinata: High Genetic Divergence on a Small Geographical Scale
Freshwater Biology (2015) 60, 1364–1378 doi:10.1111/fwb.12574 Population structuring in the monogonont rotifer Synchaeta pectinata: high genetic divergence on a small geographical scale † † DOROTHEA KIMPEL*, , JULIA GOCKEL*, GABRIELE GERLACH AND OLAF R. P. BININDA-EMONDS* *Systematics and Evolutionary Biology, Institute for Biology and Environmental Sciences (IBU), Carl von Ossietzky University Oldenburg, Oldenburg, Germany † Animal Biodiversity and Evolutionary Biology, Institute for Biology and Environmental Sciences (IBU), Carl von Ossietzky University Oldenburg, Oldenburg, Germany SUMMARY 1. Like many other zooplankton species, individual species of planktonic freshwater rotifers often possess a cosmopolitan distribution despite inhabiting isolated habitats (e.g. ponds or lakes) that present little opportunity for direct gene flow. This ‘everything is everywhere’ distribution is typi- cally ascribed to aspects of the life history of these animals (heterogonic reproductive strategy) in combination with the high dispersal capabilities presented by a dormant stage (resting eggs). 2. Recent molecular analyses indicate the presence of strong population structuring in many rotifer species, including both phylogeographic structuring and the potential for cryptic speciation. Building on these studies, we investigated the intraspecific genetic structuring in the mitochondrial barcoding marker cytochrome c oxidase subunit I (COI) among mid-European populations of the cosmopolitan rotifer Synchaeta pectinata (Rotifera, Monogononta). These data were analysed using a combination of phylogenetic analysis and haplotype networks as well as population-genetic methods to assess the degree of population and geographic structuring. 3. Gene flow among four neighbouring populations in north-west Germany (126 individuals; regional scale) and between them and a set of populations from northern Italy (an additional 48 individuals based on literature data; mid-European scale) was generally low. -
On the Conservation Value of Historic Canals for Aquatic Ecosystems T ⁎ Hsien-Yung Lina, , Steven J
Biological Conservation 251 (2020) 108764 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Perspective On the conservation value of historic canals for aquatic ecosystems T ⁎ Hsien-Yung Lina, , Steven J. Cookea, Christian Wolterb, Nathan Youngc, Joseph R. Bennetta a Institute of Environmental and Interdisciplinary Science and Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada b Department of Biology and Ecology of Fishes, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12587 Berlin, Germany c School of Sociological and Anthropological Studies, University of Ottawa, 120 University Private, Ottawa, Ontario K1N 6N5, Canada ARTICLE INFO ABSTRACT Keywords: While fragmentation and habitat loss due to water infrastructure threaten freshwater biodiversity worldwide, Anthropogenic waterways historic canals have the potential to contribute to both cultural heritage and biodiversity conservation. Shifting Novel habitat management objectives regarding historic canals from development to recreation and conservation offer op- Aquatic connectivity portunities for achieving conservation targets in these anthropogenic systems. However, managing historic ca- Cultural value nals often involves multiple objectives (e.g., nature conservation vs historic preservation). We reviewed ecolo- Structured decision making gical studies in various types of canal systems, examined the potential of historic canals to contribute to Multi-objective management biodiversity conservation, and provided suggestions to promote biodiversity conservation given the opportu- nities and challenges in canal management. Canal characteristics (e.g., size, main use, surrounding environment, physical and hydrological properties) can be used to qualify or quantify their potential conservation value and risk. Changing management regimes to mimic natural flow, enhance habitat complexity, and modify con- nectivity could improve ecosystem functions and services in canals. -
Check List Lists of Species Check List 12(4): 1942, 4 August 2016 Doi: ISSN 1809-127X © 2016 Check List and Authors
12 4 1942 the journal of biodiversity data 4 August 2016 Check List LISTS OF SPECIES Check List 12(4): 1942, 4 August 2016 doi: http://dx.doi.org/10.15560/12.4.1942 ISSN 1809-127X © 2016 Check List and Authors A revised and updated checklist of Monogononta rotifers from Argentina Noelia S. Ferrando* and María C. Claps Instituto de Limnología Dr. Raúl A. Ringuelet (CCT- CONICET La Plata, FCNyM UNLP), Boulevard 120 y 62, 1900 La Plata, Provincia de Buenos Aires, Argentina * Corresponding author. E-mail: [email protected] Abstract: We provide here a checklist of species of Koste and José de Paggi (1982) and José de Paggi and Monogononta rotifers from lentic and lotic environ- Koste (1995) compiled the then existing information ments in Argentina, 25 years after the initial catalogue on the Monogononta, reporting 624 species while compiled by Susana B. José de Paggi. This new inven- suggesting that the information was fragmentary and tory now includes the reports on rotifers documented many areas still lacked investigation. Later, checklists in 93 studies produced after 1990. The majority of the were given for Jamaica (Koste et al. 1993), Mexico investigations were carried out in three of the 24 Argen- (Sarma 1999), Guatemala and Belize (García-Morales tine provinces. In addition, the presence of 13 species and Elías-Gutiérrez 2007), Brazil (Garraffoni and in samples from three water bodies within Buenos Aires Lourenço 2012) and a Bolivian floodplain lake (Segers province are now cited here for the first time in Argen- et al. 1998). tina. In this updated checklist, a total of 351 species are In Argentina, knowledge of the rotifer fauna remains catalogued, the majority being representatives of the relatively scanty (Aoyagui and Bonecker 2004), no Lecanidae, Brachionidae, and Lepadellidae. -
Life Cycles of Planktonic Rotifers in Lake Peipsi
DISSERTATIONES BIOLOGICAE UNIVERSITATIS TARTUENSIS 55 LIFE CYCLES OF PLANKTONIC ROTIFERS IN LAKE PEIPSI TAAVI VIRRO TARTU 1999 DISSERTATIONES BIOLOGICAE UNIVERSITATIS TARTUENSIS 55 DISSERTATIONES BIOLOGICAE UNIVERSITATIS TARTUENSIS 55 LIFE CYCLES OF PLANKTONIC ROTIFERS IN LAKE PEIPSI TAAVI VIRRO TARTU UNIVERSITY PRESS Chair of Hydrobiology, Department of Zoology and Hydrobiology, University of Tartu, Estonia The dissertation was accepted for commencement of the degree of Doctor of Philosophy in Hydrobiology on May 31, 1999, by the Council of the Faculty of Biology and Geography, University of Tartu Opponent: Paula Kankaala, Ph. D., senior researcher, Lammi Biological Station, University of Helsinki, Finland Commencement: room 301, Vanemuise St. 46 at 10.15 on October 29,1999 Publication of this dissertation is granted by the University of Tartu © Taavi Virro, 1999 Tartu Ülikooli Kirjastuse trükikoda Tiigi 78, 50410 Tartu Tellimus nr. 603 CONTENTS LIST OF ORIGINAL PUBLICATIONS....................................................... 6 INTRODUCTION........................................................................................... 7 THE LAKE....................................................................................................... 10 MATERIALS AND METHODS .................................................................. 11 RESULTS AND DISCUSSION.................................................................... 13 Taxonomic composition............................................................................ 13 Seasonal -
Volume 2, Chapter 4-7A: Invertebrates: Rotifer Taxa
Glime, J. M. 2017. Invertebrates: Rotifer Taxa – Monogononta. Chapt. 4-7a. In: Glime, J. M. Bryophyte Ecology. Volume 2. 4-7a-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 4-7a INVERTEBRATES: ROTIFER TAXA – MONOGONONTA TABLE OF CONTENTS CLASS MONOGONONTA ............................................................................................................................. 4-7a-2 Order Collothecacea ................................................................................................................................... 4-7a-2 Collothecidae ...................................................................................................................................... 4-7a-2 Collotheca .................................................................................................................................... 4-7a-3 Stephanoceros .............................................................................................................................. 4-7a-5 Order Flosculariacea .................................................................................................................................. 4-7a-6 Conochilidae ....................................................................................................................................... 4-7a-6 Flosculariidae ..................................................................................................................................... -
VIEW Open Access Long-Distance Passive Dispersal in Microscopic Aquatic Animals Diego Fontaneto
Fontaneto Movement Ecology (2019) 7:10 https://doi.org/10.1186/s40462-019-0155-7 REVIEW Open Access Long-distance passive dispersal in microscopic aquatic animals Diego Fontaneto Abstract Given their dormancy capability (long-term resistant stages) and their ability to colonise and reproduce, microscopic aquatic animals have been suggested having cosmopolitan distribution. Their dormant stages may be continuously moved by mobile elements through the entire planet to any suitable habitat, preventing the formation of biogeographical patterns. In this review, I will go through the evidence we have on the most common microscopic aquatic animals, namely nematodes, rotifers, and tardigrades, for each of the assumptions allowing long- distance dispersal (dormancy, viability, and reproduction) and all the evidence we have for transportation, directly from surveys of dispersing stages, and indirectly from the outcome of successful dispersal in biogeographical and phylogeographical studies. The current knowledge reveals biogeographical patterns also for microscopic organisms, with species-specific differences in ecological features that make some taxa indeed cosmopolitan with the potential for long-distance dispersal, but others with restricted geographic distributions. Keywords: Biogeography, Cosmopolitism, Dormancy, Meiofauna, Nematoda, Phylogeography, Rotifera, Tardigrada Introduction marine species [8], for which it is known as the meiofauna Microscopic animals are generally assumed to be ex- paradox: microscopic benthic organisms with little -
Functional Groups of Rotifers and an Exotic Species in a Tropical Shallow Lake
www.nature.com/scientificreports OPEN Functional groups of rotifers and an exotic species in a tropical shallow lake Marlene Sofa Arcifa1, Bruno Barretto de Souza1*, Cláudio Simões de Morais‑Junior2 & Cyntia Goulart Corrêa Bruno3 In freshwater environments the rotifer group may be divided into microphagous and raptorial species regarding their feeding patterns, and such guilds diferently interact with other community components. Here, we analyzed the infuence of cladocerans, cyclopoid nauplii, temperature, food resources and an exotic species on rotifer guilds, based on weekly samplings for 1 year. We have identifed rotifer species and their trophi types in order to separate them into the raptorial and microphagous functional groups. The ratio raptorial:microphagous rotifers (Guild ratio, GR) was used in interaction analyses with cladocerans, nauplii, temperature, food resources and the exotic species Kellicottia bostoniensis. Correlations between total rotifers and food (phytoplankton carbon) and temperature were negative and signifcant, therefore, these factors did not lead to the increase of rotifer community. On the other hand, microphagous rotifers had opposing relation to cladoceran densities, as GR values showed that they became predominant when cladoceran populations declined. The use of density‑based GR was adequate, with similar results compared to biomass‑based studies regarding interactions with other organisms. Furthermore, we have found no invasive characteristics for the exotic microphagous rotifer, Kellicottia bostoniensis, and it seems to be outcompeted by the native microphagous species. Rotifers are an important component of plankton in aquatic environments and a link in energy fow1. Tey are more opportunistic organisms than copepods and cladocerans, mainly due to their high reproductive rate 2 and also by their capacity to inhabit special environments, such as sewage ponds and soda lakes1. -
Kellicottia Bostoniensis (Rousselet, 1908) Through Neotropical Basins
BioInvasions Records (2020) Volume 9, Issue 2: 287–302 CORRECTED PROOF Research Article Small in size but rather pervasive: the spread of the North American rotifer Kellicottia bostoniensis (Rousselet, 1908) through Neotropical basins Rafael Lacerda Macêdo1, Ana Clara S. Franco2, Gabriel Klippel1, Ewerton F. Oliveira1, Lúcia Helena S. Silva3, Luciano Neves dos Santos2,* and Christina W.C. Branco1 1Núcleo de Estudos Limnológicos; Universidade Federal do Estado do Rio de Janeiro (UNIRIO), Av. Pasteur, 458, 22290-240, Rio de Janeiro, RJ, Brasil 2Laboratório de Ictiologia Teórica e Aplicada, Universidade Federal do Estado do Rio de Janeiro (UNIRIO), Av. Pasteur, 458 - R314A, 22290-240, Rio de Janeiro, RJ, Brasil 3Laboratório de Ficologia, Museu Nacional, Universidade Federal do Rio de Janeiro (UFRJ), Quinta da Boa Vista, Horto Botânico, 20940-040, Rio de Janeiro, RJ, Brasil Author e-mails: [email protected] (RLM), [email protected] (ACSF), [email protected] (GK), [email protected] (EFO), [email protected] (LHSS), [email protected] (LNS), [email protected] (CWCB) *Corresponding author Citation: Macêdo RL, Franco ACS, Klippel G, Oliveira EF, Silva LHS, dos Abstract Santos LN, Branco CWC (2020) Small in size but rather pervasive: the spread of the Kellicottia bostoniensis is a North American limnetic zooplankter and the single North American rotifer Kellicottia rotifer species within the group of 163 non-native species recorded in Brazilian bostoniensis (Rousselet, 1908) through inland waters by the Brazilian Environmental Ministry in 2016. This species is also Neotropical basins. BioInvasions Records the only non-native rotifer of the genus Kellicottia recorded in Brazilian basins. 9(2): 287–302, https://doi.org/10.3391/bir. -
Kellicotia Bostoniensis (Rousselet, 1908) (Rotifera: Brachionidae) in Waterbodies of European Russia S
ISSN 19950829, Inland Water Biology, 2011, Vol. 4, No. 1, pp. 39–46. © Pleiades Publishing, Ltd., 2011. Original Russian Text © S.M. Zhdanova, A.E. Dobrynin, 2011, published in Biologiya Vnutrennikh Vod, No. 1, 2011, pp. 45–52. ZOOPLANKTON, ZOOBENTHOS, AND ZOOPERIPHYTON Kellicotia bostoniensis (Rousselet, 1908) (Rotifera: Brachionidae) in Waterbodies of European Russia S. M. Zhdanova and A. E. Dobrynin Papanin Institute for Biology of Inland Waters, Russian Academy of Sciences, Borok, Nekouzskii raion, Yaroslavl oblast, 152742 Russia email: [email protected] Received April 14, 2009 Abstract—The rotifer Kellicottia bostoniensis (Rousselet, 1908), which is common in North American water bodies, has been recorded in 13 different lakes of the European part of Russia. A morphometric analysis has been made of populations from 7 lakes. The assumption has been made that the size of the spines of K. bos toniensis in small waterbodies depends on the presence of predators. Depthrelated changes in density and viscosity in deep lakes with temperature stratification can also influence this feature. Keywords: Kellicottia bostoniensis, new locations, morphological variability, spatial distribution, waterbodies of European Russia. DOI: 10.1134/S1995082911010147 INTRODUCTION of the shell ranges from 400 to 1000 μm [28]. K. bos toniensis is known in the mineralized waterbodies of The genus Kellicottia Ahlstrom, 1938 (family Bra the Holarctic region [5]. The species has four unequal chionidae) includes two species, K. longispina (Kelli anterior spines (Fig. 1), and the length of the shell, cott, 1879) and K. bostoniensis (Rousselet, 1908) including the length of the spines, is ≤380 μm [28]. [5, 28]. K. longispina is a widespread inhabitant of It has been suggested [38] that K.