Keya Jackson Postdefense 4-26
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Special Issue Featuring: a Case Study on Black Gill in Georgia Shrimp
Volume 29 • Number 4 • Winter 2015 Special Issue Featuring: A Case Study on Black Gill in Georgia Shrimp Volume 29 • Number 4 • Winter 2015 The Mystery of Black Gill: Shrimpers in the South Atlantic Face Off with a Cryptic Parasite BY JILL M. GAMBILL, ALLISON E. DOYLE, RICHARD F. LEE, PH.D., PATRICK J. GEER, ANNA N. WALKER, PH.D., LINDSEY G. PARKER, PH.D., AND MARC E. FRISCHER, PH.D. ABSTRACT In the Southeast United States, an unidentified parasite is infecting shrimp and presenting new challenges for an already struggling industry. Emerging research in Georgia is investigating the resulting condition, known as Black Gill, to better understand this newest threat to the state’s most valuable commercial fishery. Researchers, shrimpers, extension agents, and fishery managers are working collaboratively to gather baseline data on where, when, and how frequently Black Gill is occurring, as well as partnering to determine its epidemiology, dispersal, and possible intervention strategies. Savannah, Ga. – In 2013, after years of intense competition from lower priced imports and financial pressures stemming Figure 1. A Georgia white shrimp displays symptoms of the from the rising cost of fuel and insurance, Georgia shrimpers Black Gill condition around its gills. Courtesy of Rachael were poised for a comeback as they looked forward to a Randall and Chelsea Parrish, 2015 profitable year. Shrimp prices had tripled, as a consequence of a bacterial disease infecting the supply of farmed shrimp A LANDMARK YEAR from Asia (Loc et al. 2013). Commercial food shrimp landings in 2013 were the lowest Georgia shrimpers took to the water with high expectations, in recent history. -
Penaeid Shrimp in Chesapeake Bay: Population Growth and Black Gill Disease Syndrome
W&M ScholarWorks VIMS Articles Virginia Institute of Marine Science 2021 Penaeid Shrimp in Chesapeake Bay: Population Growth and Black Gill Disease Syndrome Troy D. Tuckey Virginia Institute of Marine Science Jillian L. Swinford Mary C. Fabrizio Virginia Institute of Marine Science Hamish J. Small Virginia Institute of Marine Science Jeffrey D. Shields Virginia Institute of Marine Science Follow this and additional works at: https://scholarworks.wm.edu/vimsarticles Part of the Aquaculture and Fisheries Commons, and the Marine Biology Commons Recommended Citation Tuckey, Troy D.; Swinford, Jillian L.; Fabrizio, Mary C.; Small, Hamish J.; and Shields, Jeffrey D., Penaeid Shrimp in Chesapeake Bay: Population Growth and Black Gill Disease Syndrome (2021). Marine and Coastal Fisheries, 13, 159-173. DOI: 10.1002/mcf2.10143 This Article is brought to you for free and open access by the Virginia Institute of Marine Science at W&M ScholarWorks. It has been accepted for inclusion in VIMS Articles by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. Marine and Coastal Fisheries 13:159–173, 2021 © 2021 The Authors. Marine and Coastal Fisheries published by Wiley Periodicals LLC on behalf of American Fisheries Society ISSN: 1942-5120 online DOI: 10.1002/mcf2.10143 ARTICLE Penaeid Shrimp in Chesapeake Bay: Population Growth and Black Gill Disease Syndrome Troy D. Tuckey* Virginia Institute of Marine Science, William & Mary, 1370 Greate Road, Gloucester Point, Virginia 23062, USA Jillian L. Swinford Texas Parks and Wildlife, Coastal Fisheries Division, Perry R. Bass Marine Fisheries Research Center, 3864 Farm to Market Road 3280, Palacios, Texas 77465, USA Mary C. -
Prevalent Ciliate Symbiosis on Copepods: High Genetic Diversity and Wide Distribution Detected Using Small Subunit Ribosomal RNA Gene
Prevalent Ciliate Symbiosis on Copepods: High Genetic Diversity and Wide Distribution Detected Using Small Subunit Ribosomal RNA Gene Zhiling Guo1,2, Sheng Liu1, Simin Hu1, Tao Li1, Yousong Huang4, Guangxing Liu4, Huan Zhang2,4*, Senjie Lin2,3* 1 Key Laboratory of Marine Bio-resources Sustainable Utilization, South China Sea Institute of Oceanology, Chinese Academy of Science, Guangzhou, Guangdong, China, 2 Department of Marine Sciences, University of Connecticut, Groton, Connecticut, United States of America, 3 Marine Biodiversity and Global Change Laboratory, Xiamen University, Xiamen, Fujian, China, 4 Department of Environmental Science, Ocean University of China, Qingdao, Shandong, China Abstract Toward understanding the genetic diversity and distribution of copepod-associated symbiotic ciliates and the evolutionary relationships with their hosts in the marine environment, we developed a small subunit ribosomal RNA gene (18S rDNA)- based molecular method and investigated the genetic diversity and genotype distribution of the symbiotic ciliates on copepods. Of the 10 copepod species representing six families collected from six locations of Pacific and Atlantic Oceans, 9 were found to harbor ciliate symbionts. Phylogenetic analysis of the 391 ciliate 18S rDNA sequences obtained revealed seven groups (ribogroups), six (containing 99% of all the sequences) belonging to subclass Apostomatida, the other clustered with peritrich ciliate Vorticella gracilis. Among the Apostomatida groups, Group III were essentially identical to Vampyrophrya pelagica, and the other five groups represented the undocumented ciliates that were close to Vampyrophrya/ Gymnodinioides/Hyalophysa. Group VI ciliates were found in all copepod species but one (Calanus sinicus), and were most abundant among all ciliate sequences obtained, indicating that they are the dominant symbiotic ciliates universally associated with copepods. -
Handbook of Shrimp Diseases
LOAN COPY ONLY TAMU-H-95-001 C3 Handbook of Shrimp Diseases Aquaculture S.K. Johnson Department of Wildlife and Fisheries Sciences Texas A&M University 90-601 (rev) Introduction 2 Shrimp Species 2 Shrimp Anatomy 2 Obvious Manifestations ofShrimp Disease 3 Damaged Shells , 3 Inflammation and Melanization 3 Emaciation and Nutritional Deficiency 4 Muscle Necrosis 5 Tumors and Other Tissue Problems 5 Surface Fouling 6 Cramped Shrimp 6 Unusual Behavior 6 Developmental Problems 6 Growth Problems 7 Color Anomalies 7 Microbes 8 Viruses 8 Baceteria and Rickettsia 10 Fungus 12 Protozoa 12 Haplospora 13 Gregarina 15 Body Invaders 16 Surface Infestations 16 Worms 18 Trematodes 18 Cestodes 18 Nematodes 18 Environment 20 Publication of this handbook is a coop erative effort of the Texas A&M Univer sity Sea Grant College Program, the Texas A&M Department of Wildlife and $2.00 Fisheries Sciences and the Texas Additional copies available from: Agricultural Extension Service. Produc Sea Grant College Program tion is supported in part by Institutional 1716 Briarcrest Suite 603 Grant No. NA16RG0457-01 to Texas Bryan, Texas 77802 A&M University by the National Sea TAMU-SG-90-601(r) Grant Program, National Oceanic and 2M August 1995 Atmospheric Administration, U.S. De NA89AA-D-SG139 partment of Commerce. A/1-1 Handbook ofShrimp Diseases S.K. Johnson Extension Fish Disease Specialist This handbook is designed as an information source and tail end (abdomen). The parts listed below are apparent upon field guide for shrimp culturists, commercial fishermen, and outside examination (Fig. 1). others interested in diseases or abnormal conditions of shrimp. -
Phylogenetic Position of the Apostome Ciliates (Phylum Ciliophora, Subclass Apostomatia) Tested Using Small Subunit Rrna Gene Sequences*
©Biologiezentrum Linz/Austria, download unter www.biologiezentrum.at Phylogenetic position of the apostome ciliates (Phylum Ciliophora, Subclass Apostomatia) tested using small subunit rRNA gene sequences* J o h n C . C L AM P , P h y l l i s C . B RADB UR Y , M i c h a e l a C . S TR ÜDER -K Y P KE & D e n i s H . L Y N N Abstract: The apostomes have been assigned historically to two major groups of ciliates – now called the Class Phyllopharyngea and Class Oligohymenophorea. We set about to test these competing hypotheses of relationship using sequences of the small sub- unit rRNA gene from isolates of five species of apostomes: Gymnodinioides pitelkae from Maine; Gymnodinioides sp. from North Ca- rolina; Hyalophysa chattoni from Florida and from North Carolina; H. lwoffi from North Carolina; and Vampyrophrya pelagica from North Carolina. These apostome ciliates were unambiguously related to taxa in the Class Oligohymenophorea using Bayesian in- ference, maximum parsimony, and neighbor-joining algorithms to infer phylogenetic relationship. Thus, their assignment as the Subclass Apostomatia within this class is confirmed by these genetic data. The two isolates of Hyalophysa chattoni were harvested from the same crustacean host, Palaemonetes pugio, at localities separated by slightly more than 1225 km, and yet they showed only 0.06% genetic divergence, suggesting that they represent a single population. Key words: Apostomes, crustacean, exuviotroph, Gammarus mucronatus, Marinogammarus obtusatus, Oligohymenophorea. Introduction In morphologically-based classifications, apostome ciliates have been placed with either one or the other Over the past 20 years, sequences of the small sub- of two major taxa, now considered classes (BRADBURY unit rRNA (SSrRNA) gene have been used to confirm 1989). -
Fusiforma Themisticola N. Gen., N. Sp., a New Genus and Species Of
Protist, Vol. 164, 793–810, November 2013 http://www.elsevier.de/protis Published online date 23 October 2013 ORIGINAL PAPER Fusiforma themisticola n. gen., n. sp., a New Genus and Species of Apostome Ciliate Infecting the Hyperiid Amphipod Themisto libellula in the Canadian Beaufort Sea (Arctic Ocean), and Establishment of the Pseudocolliniidae (Ciliophora, Apostomatia) a,1 b,c d Chitchai Chantangsi , Denis H. Lynn , Sonja Rueckert , e a f Anna J. Prokopowicz , Somsak Panha , and Brian S. Leander a Department of Biology, Faculty of Science, Chulalongkorn University, Phayathai Road, Pathumwan, Bangkok 10330, Thailand b Department of Zoology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada c Department of Integrative Biology, University of Guelph, Guelph, ON N1G 2W1, Canada d School of Life, Sport and Social Sciences, Edinburgh Napier University, Sighthill Campus, Sighthill Court, Edinburgh EH11 4BN, Scotland, United Kingdom e Québec-Océan, Département de Biologie, Université Laval, Quebec, QC G1V 0A6, Canada f Canadian Institute for Advanced Research, Departments of Zoology and Botany, University of British Columbia, Vancouver, BC V6T 1Z4, Canada Submitted May 30, 2013; Accepted September 16, 2013 Monitoring Editor: Genoveva F. Esteban A novel parasitic ciliate Fusiforma themisticola n. gen., n. sp. was discovered infecting 4.4% of the hyperiid amphipod Themisto libellula. Ciliates were isolated from a formaldehyde-fixed whole amphi- pod and the DNA was extracted for amplification of the small subunit (SSU) rRNA gene. Sequence and phylogenetic analyses showed unambiguously that this ciliate is an apostome and about 2% diver- gent from the krill-infesting apostome species assigned to the genus Pseudocollinia. Protargol silver impregnation showed a highly unusual infraciliature for an apostome. -
Microzooplankton Distribution in the Amundsen Sea Polynya (Antarctica) During an Extensive Phaeocystis Antarctica Bloom
Microzooplankton distribution in the Amundsen Sea Polynya (Antarctica) during an extensive Phaeocystis antarctica bloom Rasmus Swalethorp *1,2,3 , Julie Dinasquet *1,4,5 , Ramiro Logares 6, Stefan Bertilsson 7, Sanne Kjellerup 2,3 , Anders K. Krabberød 8, Per-Olav Moksnes 3, Torkel G. Nielsen 2, and Lasse Riemann 4 1 Scripps Institution of Oceanography, University of California San Diego, USA 2 National Institute of Aquatic Resources (DTU Aqua), Technical University of Denmark, Denmark 3 Department of Marine Sciences, University of Gothenburg, Sweden 4 Marine Biological Section, Department of Biology, University of Copenhagen, Denmark 5 Department of Natural Sciences, Linnaeus University, Sweden 6 Institute of Marine Sciences (ICM), CSIC, Spain 7 Department of Ecology and Genetics: Limnology and Science for Life Laboratory, Uppsala University, Sweden 8 Department of Biosciences, Section for Genetics and Evolutionary Biology (Evogene), University of Oslo, Norway *Equal contribution, correspondence: [email protected], [email protected] Key words: ciliate; dinoflagellate; growth rates; Southern Ocean; Antarctica; Amundsen Sea polynya; Gymnodinium spp. 1 Abbreviations: ASP: Amundsen Sea Polynya; SO: Southern Ocean; HNF: Heterotrophic nanoflagellates; OTU: Operational Taxonomic Unit, DFM: Deep Fluorescence Maximum 2 Abstract In Antarctica, summer is a time of extreme environmental shifts resulting in large coastal phytoplankton blooms fueling the food web. Despite the importance of the microbial loop in remineralizing biomass from primary production, studies of how microzooplankton communities respond to such blooms in the Southern Ocean are rather scarce. Microzooplankton (ciliate and dinoflagellate) communities were investigated combining microscopy and 18S rRNA sequencing analyses in the Amundsen Sea Polynya during an extensive summer bloom of Phaeocystis antarctica . -
Ciliophora, Scuticociliatia)
Available online at www.sciencedirect.com ScienceDirect European Journal of Protistology 50 (2014) 174–184 Morphology, ontogenesis and molecular phylogeny of Platynematum salinarum nov. spec., a new scuticociliate (Ciliophora, Scuticociliatia) from a solar saltern a,∗ b c c c Wilhelm Foissner , Jae-Ho Jung , Sabine Filker , Jennifer Rudolph , Thorsten Stoeck a Universität Salzburg, FB Organismische Biologie, Hellbrunnerstrasse 34, A-5020 Salzburg, Austria b Inha University, Biological Sciences, 402-251 Incheon, South Korea c Universität Kaiserslautern, FB Biologie, Erwin-Schrödingerstrasse 14, D-67663 Kaiserslautern, Germany Received 8 July 2013; received in revised form 19 September 2013; accepted 1 October 2013 Available online 11 October 2013 Abstract Platynematum salinarum nov. spec. was discovered in a hypersaline (∼120‰) solar saltern in Portugal. Its morphology, ontogenesis, and 18S rRNA were studied with routine methods. Platynematum salinarum has a size of about 35 m × 18 m and differs from other platynematids (= Platynematum and Pseudoplatynematum) in having an only slightly flattened body without any spines or notches. Both, the oral and somatic infraciliature resemble other platynematids and the tetrahymenid pattern in general. The ontogenesis is scuticobuccokinetal, being unique in generating protomembranelle 1 from kinetids produced by the paroral membrane of the proter and of the scutica. This composite divides transversely: the right half becomes the paroral membrane of the opisthe, the left half transforms to opisthe’s adoral membranelle 1. The scutica and the molecular sequence classify P. salinarum into the order Scuticociliatida, family Cinetochilidae. The 18S rRNA sequence shows 92.7% similarity to the closest relative deposited in public databases (the scuticociliate Sathrophilus holtae), and our study provides the first sequence for the genus Platynematum. -
Protista (PDF)
1 = Astasiopsis distortum (Dujardin,1841) Bütschli,1885 South Scandinavian Marine Protoctista ? Dingensia Patterson & Zölffel,1992, in Patterson & Larsen (™ Heteromita angusta Dujardin,1841) Provisional Check-list compiled at the Tjärnö Marine Biological * Taxon incertae sedis. Very similar to Cryptaulax Skuja Laboratory by: Dinomonas Kent,1880 TJÄRNÖLAB. / Hans G. Hansson - 1991-07 - 1997-04-02 * Taxon incertae sedis. Species found in South Scandinavia, as well as from neighbouring areas, chiefly the British Isles, have been considered, as some of them may show to have a slightly more northern distribution, than what is known today. However, species with a typical Lusitanian distribution, with their northern Diphylleia Massart,1920 distribution limit around France or Southern British Isles, have as a rule been omitted here, albeit a few species with probable norhern limits around * Marine? Incertae sedis. the British Isles are listed here until distribution patterns are better known. The compiler would be very grateful for every correction of presumptive lapses and omittances an initiated reader could make. Diplocalium Grassé & Deflandre,1952 (™ Bicosoeca inopinatum ??,1???) * Marine? Incertae sedis. Denotations: (™) = Genotype @ = Associated to * = General note Diplomita Fromentel,1874 (™ Diplomita insignis Fromentel,1874) P.S. This list is a very unfinished manuscript. Chiefly flagellated organisms have yet been considered. This * Marine? Incertae sedis. provisional PDF-file is so far only published as an Intranet file within TMBL:s domain. Diplonema Griessmann,1913, non Berendt,1845 (Diptera), nec Greene,1857 (Coel.) = Isonema ??,1???, non Meek & Worthen,1865 (Mollusca), nec Maas,1909 (Coel.) PROTOCTISTA = Flagellamonas Skvortzow,19?? = Lackeymonas Skvortzow,19?? = Lowymonas Skvortzow,19?? = Milaneziamonas Skvortzow,19?? = Spira Skvortzow,19?? = Teixeiromonas Skvortzow,19?? = PROTISTA = Kolbeana Skvortzow,19?? * Genus incertae sedis. -
Parasite Diversity of Nyctiphanes Simplex and Nematoscelis Difficilis (Crustacea: Euphausiacea) Along the Northwestern Coast of Mexico
Vol. 88: 249–266, 2010 DISEASES OF AQUATIC ORGANISMS Published February 17 doi: 10.3354/dao02155 Dis Aquat Org Parasite diversity of Nyctiphanes simplex and Nematoscelis difficilis (Crustacea: Euphausiacea) along the northwestern coast of Mexico Jaime Gómez-Gutiérrez1, 3,*, Carlos J. Robinson2, So Kawaguchi3, Stephen Nicol3 1Departamento de Plancton y Ecología Marina, Centro Interdisciplinario de Ciencias Marinas, A.P. 592, C.P. 23096, La Paz, Baja California Sur, México 2Laboratorio de Ecología de Pesquerías, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, A.P. 70-305, México D.F. C.P. 04510, México 3Australian Antarctic Division, Department of Environment, Water, Heritage and Arts, 203 Channel Highway, Kingston, Tasmania 7050, Australia ABSTRACT: The diversity of parasites found on Nyctiphanes simplex and Nematoscelis difficilis (Order Euphausiacea) was compared during 10 oceanographic cruises made off both coasts of the Baja California peninsula, Mexico. We tested the hypothesis that N. simplex has a more diverse para- sitic assemblage than N. difficilis because it is a neritic species, has larger population abundance, and tends to form denser and more compact swarms than N. difficilis. These biological and behavioral features may enhance parasite transmission within swarms. We detected 6 types of ectoparasites: (1) epibiotic diatoms Licmophora sp.; (2) Ephelotidae suctorian ciliates; (3) Foettingeriidae exu- viotrophic apostome ciliates; (4) an unidentified epicaridean cryptoniscus larvae (isopoda); and 2 cas- trators: (5) the ectoparasitic Dajidae isopod Notophryxus lateralis and (6) the ellobiopsid mesopara- site Thalassomyces fagei. We also detected 7 types of endoparasites: (1) an undescribed Collinia ciliate (Apostomatida); 3 types of Cestoda: (2) a Tetrarhynchobothruium sp. -
Classification of the Phylum Ciliophora (Eukaryota, Alveolata)
1! The All-Data-Based Evolutionary Hypothesis of Ciliated Protists with a Revised 2! Classification of the Phylum Ciliophora (Eukaryota, Alveolata) 3! 4! Feng Gao a, Alan Warren b, Qianqian Zhang c, Jun Gong c, Miao Miao d, Ping Sun e, 5! Dapeng Xu f, Jie Huang g, Zhenzhen Yi h,* & Weibo Song a,* 6! 7! a Institute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, 8! China; b Department of Life Sciences, Natural History Museum, London, UK; c Yantai 9! Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, China; d 10! College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China; 11! e Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, 12! Xiamen University, Xiamen, China; f State Key Laboratory of Marine Environmental 13! Science, Institute of Marine Microbes and Ecospheres, Xiamen University, Xiamen, 14! China; g Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China; h 15! School of Life Science, South China Normal University, Guangzhou, China. 16! 17! Running Head: Phylogeny and evolution of Ciliophora 18! *!Address correspondence to Zhenzhen Yi, [email protected]; or Weibo Song, 19! [email protected] 20! ! ! 1! Table S1. List of species for which SSU rDNA, 5.8S rDNA, LSU rDNA, and alpha-tubulin were newly sequenced in the present work. ! ITS1-5.8S- Class Subclass Order Family Speicies Sample sites SSU rDNA LSU rDNA a-tubulin ITS2 A freshwater pond within the campus of 1 COLPODEA Colpodida Colpodidae Colpoda inflata the South China Normal University, KM222106 KM222071 KM222160 Guangzhou (23° 09′N, 113° 22′ E) Climacostomum No. -
1 Life Cycle of the Suctorian Ciliate Ephelota Plana Attached to the Krill
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Woods Hole Open Access Server 1 Life cycle of the suctorian ciliate Ephelota plana attached to the krill Euphausia pacifica Yoshinari Endoa,*, Daiki Fujiia,1, Goh Nishitania, Peter H. Wiebeb aLaboratory of Biological Oceanography, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555, Japan, bWoods Hole Oceanographic Institution, Woods Hole, MA 02543, U.S.A. *Corresponding author at: Laboratory of Biological Oceanography, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555, Japan E-mail address: [email protected] 1Present address: Marine Biological Research Institute of Japan Co. Ltd., Tokyo, 142-0042, Japan Running title: Life cycle of Ephelota plana 2 ABSTRACT The hypothesis that life cycle of an epibiotic suctorian ciliate Ephelota plana is adapted to the molt cycle of the krill Euphausia pacifica collected in Saanich Inlet, Canada was evaluated. The infestation prevalence of E. plana and the number of individuals attached increased from postmolt stage to premolt stage of E. pacifica, and concurrently cell growth of E. plana was observed. Budding individuals of E. plana first appeared at early premolt stage and increased to 21% at late premolt stage. Thus the life cycle of E. plana seems to be adapted to the molt cycle of E. pacifica. KEYWORDS: suctorians, Ephelota plana, life cycle, Euphausia pacifica, molt cycle 3 1. Introduction Various ciliates are known to infest euphausiids, an important marine crustacean group in marine ecosystems, ranging from highly lethal ones such as Pseudocollinia spp., which kill the euphausiid host within 40 h of infestation (Gómez-Gutiérrez et al.