A Molecular and Phylogenetic Analysis of Cryobiosis in Nematodes of the Genus Panagrolaimus

Total Page:16

File Type:pdf, Size:1020Kb

A Molecular and Phylogenetic Analysis of Cryobiosis in Nematodes of the Genus Panagrolaimus A Molecular and Phylogenetic Analysis of Cryobiosis in Nematodes of the Genus Panagrolaimus Lorraine Marie McGill, B. Sc. Thesis submitted to the National University of Ireland Maynooth in fulfilment of the requirements for the Degree of Doctor of Philosophy Department of Biology National University of Ireland Maynooth Co. Kildare Supervisor: Prof. Ann Burnell Head of Department: Prof. Kay Ohlendieck October 2011 Table of Contents Abbreviations ........................................................................................................... i! List of Figures......................................................................................................... iv! List of Tables ........................................................................................................ viii! Acknowledgements.................................................................................................. x! Declaration............................................................................................................. xii! Abstract................................................................................................................. xiii! Chapter I General Introduction .............................................................1! 1.1 Nematodes.......................................................................................................... 1! 1.1.1 Habitat and ecology ..................................................................................... 1! 1.1.2 Nematode morphology................................................................................. 1! 1.1.3 Molecular taxonomy of the Phylum Nematoda ........................................... 2! 1.1.3.1 Ribosomal small subunit gene .............................................................. 2! 1.1.3.2 Ribosomal large subunit gene ............................................................... 4! 1.1.3.3 rRNA internal transcribed spacer.......................................................... 4! 1.1.3.4 Mitochondrial cytochrome c oxidase subunit 1 .................................... 5! 1.1.4 Panagrolaimus sp. ....................................................................................... 5! 1.2 Phylogenetics .................................................................................................. 7! 1.2.1 Methods used in phylogenetic studies ......................................................... 7! 1.2.1.1 Maximum likelihood methods .............................................................. 8! 1.2.1.2 Bayesian methods ................................................................................. 9! 1.2.2 The fossil record and evolutionary timescales............................................. 9! 1.2.2.1 Molecular clock models ...................................................................... 10! 1.2.2.2 Molecular clock calibration ................................................................ 12! 1.2.3 Nematode evolution ................................................................................... 13! 1.3 Freezing survival ............................................................................................. 15! 1.3.1 Definition and occurrence of freezing-adapted organisms ........................ 17! 1.3.1.1 Microorganisms .................................................................................. 17! 1.3.1.2 Plants................................................................................................... 17! 1.3.1.3 Animals ............................................................................................... 19! 1.3.2 Why study freeze tolerance? ...................................................................... 20! 1.4 Freezing injury ................................................................................................ 20! 1.5 Mechanisms of freezing tolerance ................................................................. 21! 1.5.1 Accumulation of colligative cryoprotectants ............................................. 22! 1.5.1.1 Colligative cryoprotectants ................................................................. 22! 1.5.1.2 Glycerol............................................................................................... 22! 1.5.1.3 Sorbitol................................................................................................ 24! 1.5.1.4 Glucose................................................................................................ 24! 1.5.2 Accumulation of low-molecular weight cryoprotectants........................... 25! 1.5.2.1 Trehalose............................................................................................. 25! 1.5.2.2 Proline ................................................................................................. 28! 1.5.2.3 Glycine betaine ................................................................................... 30! 1.5.3 Antifreeze proteins..................................................................................... 30! 1.5.3.1 Mechanism that Antifreeze proteins bind to the ice............................ 31! 1.5.3.2 Fish antifreeze proteins ....................................................................... 36! 1.5.3.3 Fish Type I antifreeze proteins............................................................ 36! 1.5.3.4 Fish Type II antifreeze proteins .......................................................... 38! 1.5.3.5 Fish Type III antifreeze proteins......................................................... 38! 1.5.3.6 Fish Type IV antifreeze proteins......................................................... 39! 1.5.3.7 Fish Type V antifreeze proteins .......................................................... 40! 1.5.3.8 Insect and arthropod antifreeze proteins ............................................. 41! 1.5.3.9 Plant antifreeze proteins...................................................................... 44! 1.5.3.10 Algal AFPs........................................................................................ 48! 1.5.3.11 Fungal AFPs...................................................................................... 49! 1.5.3.12 Yeast AFPs........................................................................................ 49! 1.5.3.13 Bacterial AFPs .................................................................................. 50! 1.5.4 Ice nucleator proteins ................................................................................. 50! 1.5.5 Gene and protein induction in response to low temperature stress............ 53! 1.5.5.1 Cold-shock proteins ............................................................................ 55! 1.5.5.2 Cold-regulated genes........................................................................... 55! 1.5.5.3 Heat shock proteins............................................................................. 58! 1.5.5.4 Alteration of cell membrane lipid composition .................................. 59! 1.6 Relationship between freezing and desiccation survival ............................. 62! 1.7 Freezing survival in nematodes ..................................................................... 62! 1.8 Objectives of this project................................................................................ 65! Chapter II Materials and Methods ......................................................66! 2.1 Materials .......................................................................................................... 66! 2.1.1 Chemicals................................................................................................... 66! 2.1.2 Bacterial strains and plasmids.................................................................... 66! 2.1.3 Source of Panagrolaimus species and strains............................................ 66! 2.2 Methods............................................................................................................ 68! 2.2.1 Nematode culturing methods ..................................................................... 68! 2.2.1.1 Culturing of Panagrolaimus species and strains................................. 68! 2.2.1.2 Mass culturing nematodes................................................................... 68! 2.2.1.3 Harvesting nematodes ......................................................................... 68! 2.2.1.4 Cleaning nematode stocks................................................................... 69! 2.2.1.5 Freezing nematode stocks ................................................................... 69! 2.2.1.6 Recovery of frozen nematode stocks .................................................. 70! 2.2.1.7 Desiccation stress experiments ........................................................... 70! 2.2.1.8 Freezing stress experiments ................................................................ 70! 2.2.2 Molecular methods..................................................................................... 71! 2.2.2.1 Genomic DNA extraction ................................................................... 71! 2.2.2.2 RNA extraction ................................................................................... 72! 2.2.2.3 cDNA synthesis................................................................................... 72! 2.2.2.4 Determination of RNA/DNA concentration and quality .................... 73! 2.2.2.5 Agrose gel electrophoresis .................................................................
Recommended publications
  • Insect Cold Tolerance: How Many Kinds of Frozen?
    POINT OF VIEW Eur. J. Entomol. 96:157—164, 1999 ISSN 1210-5759 Insect cold tolerance: How many kinds of frozen? B rent J. SINCLAIR Department o f Zoology, University o f Otago, PO Box 56, Dunedin, New Zealand; e-mail: [email protected] Key words. Insect, cold hardiness, strategies, Freezing tolerance, Freeze intolerance Abstract. Insect cold tolerance mechanisms are often divided into freezing tolerance and freeze intolerance. This division has been criticised in recent years; Bale (1996) established five categories of cold tolerance. In Bale’s view, freezing tolerance is at the ex­ treme end of the spectrum o f cold tolerance, and represents insects which are most able to survive low temperatures. Data in the lit­ erature from 53 species o f freezing tolerant insects suggest that the freezing tolerance strategies o f these species are divisible into four groups according to supercooling point (SCP) and lower lethal temperature (LLT): (1) Partially Freezing Tolerant-species that survive a small proportion o f their body water converted into ice, (2) Moderately Freezing Tolerant-species die less than ten degrees below their SCP, (3) Strongly Freezing Tolerant-insects with LLTs 20 degrees or more below their SCP, and (4) Freezing Tolerant Species with Low Supercooling Points which freeze at very low temperatures, and can survive a few degrees below their SCP. The last 3 groups can survive the conversion of body water into ice to an equilibrium at sub-lethal environmental temperatures. Statistical analyses o f these groups are presented in this paper. However, the data set is small and biased, and there are many other aspects o f freezing tolerance, for example proportion o f body water frozen, and site o f ice nucleation, so these categories may have to be re­ vised in the future.
    [Show full text]
  • This Is an Open Access Document Downloaded from ORCA, Cardiff University's Institutional Repository
    This is an Open Access document downloaded from ORCA, Cardiff University's institutional repository: http://orca.cf.ac.uk/117055/ This is the author’s version of a work that was submitted to / accepted for publication. Citation for final published version: Jorge, F., White, R.S.A. and Paterson, Rachel A. 2018. Hiding in the swamp: new capillariid nematode parasitizing New Zealand brown mudfish. Journal of Helminthology 92 (3) , pp. 379-386. 10.1017/S0022149X17000530 file Publishers page: http://dx.doi.org/10.1017/S0022149X17000530 <http://dx.doi.org/10.1017/S0022149X17000530> Please note: Changes made as a result of publishing processes such as copy-editing, formatting and page numbers may not be reflected in this version. For the definitive version of this publication, please refer to the published source. You are advised to consult the publisher’s version if you wish to cite this paper. This version is being made available in accordance with publisher policies. See http://orca.cf.ac.uk/policies.html for usage policies. Copyright and moral rights for publications made available in ORCA are retained by the copyright holders. Title: Hiding in the swamp: new capillariid nematode parasitizing New Zealand brown mudfish Authors: Fátima Jorge1, Richard S. A. White2 and Rachel A. Paterson1,3 Addresses: 1Department of Zoology, University of Otago, PO Box 56, Dunedin 9054, New Zealand; 2School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand; 3School of Biosciences, University of Cardiff, Cardiff, CF10 3AX, United Kingdom Running headline: Capillariid nematode parasitizing New Zealand mudfish Corresponding author: Fátima Jorge Department of Zoology, University of Otago, 340 Great King Street, PO Box 56, Dunedin 9054, New Zealand e-mail: [email protected] 1 Abstract The extent of New Zealand’s freshwater fish-parasite diversity has yet to be fully revealed, with host-parasite relationships still to be described from nearly half the known fish community.
    [Show full text]
  • Early Stages of Fishes in the Western North Atlantic Ocean Volume
    ISBN 0-9689167-4-x Early Stages of Fishes in the Western North Atlantic Ocean (Davis Strait, Southern Greenland and Flemish Cap to Cape Hatteras) Volume One Acipenseriformes through Syngnathiformes Michael P. Fahay ii Early Stages of Fishes in the Western North Atlantic Ocean iii Dedication This monograph is dedicated to those highly skilled larval fish illustrators whose talents and efforts have greatly facilitated the study of fish ontogeny. The works of many of those fine illustrators grace these pages. iv Early Stages of Fishes in the Western North Atlantic Ocean v Preface The contents of this monograph are a revision and update of an earlier atlas describing the eggs and larvae of western Atlantic marine fishes occurring between the Scotian Shelf and Cape Hatteras, North Carolina (Fahay, 1983). The three-fold increase in the total num- ber of species covered in the current compilation is the result of both a larger study area and a recent increase in published ontogenetic studies of fishes by many authors and students of the morphology of early stages of marine fishes. It is a tribute to the efforts of those authors that the ontogeny of greater than 70% of species known from the western North Atlantic Ocean is now well described. Michael Fahay 241 Sabino Road West Bath, Maine 04530 U.S.A. vi Acknowledgements I greatly appreciate the help provided by a number of very knowledgeable friends and colleagues dur- ing the preparation of this monograph. Jon Hare undertook a painstakingly critical review of the entire monograph, corrected omissions, inconsistencies, and errors of fact, and made suggestions which markedly improved its organization and presentation.
    [Show full text]
  • Phospholipid Fatty Acids As Biomass Proxies and Their Use in Characterizing Deep Terrestrial Subsurface Microbial Communities
    PHOSPHOLIPID FATTY ACIDS AS BIOMASS PROXIES AND THEIR USE IN CHARACTERIZING DEEP TERRESTRIAL SUBSURFACE MICROBIAL COMMUNITIES By SIAN E. FORD, B.Sc., B.Sc. A Thesis Submitted to the School of Graduate Studies in Partial Fulfillment of the Requirements for the Degree Master of Science McMaster University ©Copyright by Sian E. Ford, September 2018 MASTER OF SCIENCE (2018) Earth and Environmental Sciences Collaborative Graduate Program in Astrobiology McMaster University Hamilton, Ontario TITLE: PHOSPHOLIPID FATTY ACIDS AS BIOMASS PROXIES AND THEIR USE IN CHARACTERIZING DEEP TERRESTRIAL SUBSURFACE MICROBIAL COMMUNITIES AUTHOR: Sian E. Ford, B.Sc., B.Sc. (University of Alberta) SUPERVISOR: Dr. Gregory F. Slater NUMBER OF PAGES: viii, 74 ii ABSTRACT Understanding the distribution, abundances and metabolic activities of microbial life in the subsurface is fundamental to our understanding of the role microbes play in many areas of inquiry such as terrestrial biogeochemical cycling and the search for extraterrestrial life. The deep terrestrial subsurface is known to harbor microbial life at depths of up to several kilometers where, in some cases, organisms live independently from the photosphere and atmosphere. Ancient fracture fluids trapped within the crystalline basement of the Canadian Precambrian Shield have been shown to be preserved on geologic timescales (millions to billions of years). Significant challenges exist when probing the deep terrestrial subsurface including the low biomass abundance, heterogeneous distribution of biomass, and the potential for matrix effects during sampling and analysis. This Master’s thesis project has two main parts. The first study utilizes phospholipid fatty acid (PLFA) analysis to determine the extent of mineral matrices on the effectiveness of PLFA extraction and analysis from deep terrestrial subsurface samples.
    [Show full text]
  • Iiillllllllli'lllll | US005627051A United States Patent [191 [11] Patent Number: 5,627,051 Duman [45] Date of Patent: May 6, 1997
    llilll|||l|l|||||ll||||||i|lllllllllllllllllllllllllllll.nIiillllllllli'lllll | US005627051A United States Patent [191 [11] Patent Number: 5,627,051 Duman [45] Date of Patent: May 6, 1997 [54] NUCLEIC ACID SEQUENCES ENCODING LG. Duman et al.. ‘Thermal hysteresis proteins”. Advances DENDROIDES ANTIFREEZE PROTEINS in Low Temperature Biology, vol. 2. pp. 131-182, (1993). [75] Inventor: John G. Duman. South Bend. Ind. D. Tursman et al., “Cryoprotective eifects of Thermal Hys teresis Protein on Survivorship of Frozen Gut Cells from the [73] Assignee: University of Notre Dame du Lac, Freeze Tolerant Centipede Lithobius for?catus”, Journal of Notre Dame, Ind. Experimental Zoology. vol. 272, pp. 249-257 (1995). D.W. Wu et al., “Activation of antifreeze proteins from [21] Appl. No.: 485,359 larvae of the beetle Dendroides canadensis”, Comp. Physiol. [22] Filed: Jun. 7, 1995 B, vol. 161, pp. 279-283 (1991). [51] Int. Cl.6 ........................... .. C12P 21/02; C07H 21/04 D.W. Wu et al., “Puri?cation and characterization of anti [52] US. Cl. .. 435/69.1; 536/235; 536/2431 freeze proteins from larvae of the beetle Dendroides [58] Field of Search .............................. .. 435/3201, 69.1; canadensis”, Comp. Physiol. B, vol. 161, pp. 271-278 536/235. 24.31 (1991). [56] References Cited Primary Examiner—Dian C. Jacobson PUBLICATIONS Assistant Examiner-Kawai Lau J.G. Duman et al., “Hemolymph proteins involved in insect Attorney, Agent, or Firm—Barnes & Thomburg subzero tolerance: Ice nucleators and antifreeze proteins”, In Insects at Low Temperatures, Chapman and Hall (N .Y.), pp. [57] ABSTRACT 94-127 (1991). The present invention is directed to nucleic acid sequences D.W.
    [Show full text]
  • Regulation of Phosphofructokinase and the Control of Cryoprotectant Synthesis in a Freeze-Avoiding Insect
    Regulation of phosphofructokinase and the control of cryoprotectant synthesis in a freeze-avoiding insect CLARKP. HOLDENAND KENNETHB. STOREY Departments of Biology and Chemistry, Carleton Universiry, Ottawa, ON KIS 5B6, Canada Received February 23, 1993 Accepted June 23, 1993 HOLDEN,C.P., and STOREY,K.B. 1993. Regulation of phosphofructokinase and the control of cryoprotectant synthesis in a freeze-avoiding insect. Can. J. Zool. 71: 1895 - 1899. Phosphofructokinase (PFK) from larvae of the freeze-avoiding gall moth Epiblema scudderiana was purified 7 1 1-fold using ATP-agarose affinity chromatography to a final specific activity of 23 Ulmg protein. The native molecular mass of the enzyme was 420 000 + 20 000 Da. The enzyme showed an optimum pH of 8.13 + 0.2 1 at 22°C and 8.19 + 0.1 1 at 5°C. Arrhenius plots of PFK activity showed a sharp break at 9°C. So,, values for fructose 6-phosphate showed positive thermal modifica- tion, decreasing with decreasing assay temperature; the opposite was true for ATP-Mg2+. PFK was activated by fructose 2,6-bisphosphate, AMP, and inorganic phosphate; activator effects were temperature-dependent. The enzyme was inhibited by ATP-M~~+,citrate-Mg2+, and phosphoenolpyruvate. The positive effects of low temperature on enzyme kinetic proper- ties would promote PFK activity to channel glycolytic carbon flow into the production of glycerol during cold-stimulated cryoprotectant synthesis. HOLDEN,C.P., et STOREY,K.B. 1993. Regulation of phosphofructokinase and the control of cryoprotectant synthesis in a freeze-avoiding insect. Can. J. Zool. 71 : 1895 - 1899. De la phosphofructokinase (PFK) prklevke chez des larves d'Epiblema scudderiana, un papillon gallicole rkfractaire au gel, a kt6 rendue 7 1 1 fois plus concentrke par chromatographie d'affinitk a 1'ATP-agarose lui confkrant une activitk spkcifique finale de 23 Ulmg protkine.
    [Show full text]
  • A New Genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a Key to the Three Species Daniel K
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 2014 Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species Daniel K. Young University of Wisconsin - Madison Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi Young, Daniel K., "Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species" (2014). Insecta Mundi. 846. http://digitalcommons.unl.edu/insectamundi/846 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI A Journal of World Insect Systematics 0341 Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species Daniel K. Young Department of Entomology 445 Russell Laboratories University of Wisconsin Madison, Wisconsin 53706-1598 USA Date of Issue: January 31, 2014 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Daniel K. Young Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species Insecta Mundi 0341: 1-18 ZooBank Registered: urn:lsid:zoobank.org:pub:994D7E0D-D7DF-49A3-9A25-25EE0B3D7F22 Published in 2014 by Center for Systematic Entomology, Inc. P. O. Box 141874 Gainesville, FL 32614-1874 USA http://centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non-marine arthropod.
    [Show full text]
  • Coleoptera: Tenebrionidae) from Australia, Southeast Asia and the Pacific Region, with Comments on Phylogenetic Relationships and Antipredator Adaptations
    Systematic Entomology (2004) 29, 101–114 First descriptions of Coelometopini pupae (Coleoptera: Tenebrionidae) from Australia, Southeast Asia and the Pacific region, with comments on phylogenetic relationships and antipredator adaptations PATRICE BOUCHARD1,2 andWARREN E. STEINER Jr3 1Canadian Museum of Nature, Ottawa, Ontario, Canada, 2Department of Natural Resource Sciences, McGill University, Ste-Anne-de-Bellevue, Que´bec, Canada and 3Department of Systematic Biology – Entomology, Smithsonian Institution, Washington, DC, U.S.A. Abstract. The pupal stage of ten Coelometopini species occurring in Australia, New Guinea, Southeast Asia and the Pacific region are described and a key for their identification is provided. The species are Chrysopeplus expolitus Broun, Derosphaerus hirtipes Kaszab, Hypaulax crenata (Boisduval), Leprocaulus borneensis Kaszab, Metisopus purpureipennis Bates, Promethis carteri Kaszab, P. nigra (Blessig), P. quadraticollis (Gebien), P. quadricollis Pascoe and P. sulcigera (Boisduval). The gin trap structures of D. hirtipes and P. quadraticollis are described in detail using scanning electron micrographs. A summary of anti- predator structures of all known Coelometopini pupae is given. The phylogenetic value of pupal characters is assessed at intra- and intergeneric levels within the tribe. Introduction tribe Coelometopini (Tenebrionidae: Coelometopinae) to address this question. The evolution of a pupal stage in the life history of holo- metabolous insects has been of great importance for the success of insects. This critical transformation stage has Antipredator adaptations in insect pupae enabled members of Holometabola to dissociate the larval and adult stages and, as a consequence, promoted the Hinton (1955) identified two main types of antipredator exploitation of a wide variety of environments. Although device in pupae of holometabolous insects: passive and most insect pupae are immotile, a small number of clades nonpassive.
    [Show full text]
  • Inventory of Tidepool and Estuarine Fishes in Acadia National Park
    INVENTORY OF TIDEPOOL AND ESTUARINE FISHES IN ACADIA NATIONAL PARK Edited by Linda J. Kling and Adrian Jordaan School of Marines Sciences University of Maine Orono, Maine 04469 Report to the National Park Service Acadia National Park February 2008 EXECUTIVE SUMMARY Acadia National Park (ANP) is part of the Northeast Temperate Network (NETN) of the National Park Service’s Inventory and Monitoring Program. Inventory and monitoring activities supported by the NETN are becoming increasingly important for setting and meeting long-term management goals. Detailed inventories of fishes of estuaries and intertidal areas of ANP are very limited, necessitating the collection of information within these habitats. The objectives of this project were to inventory fish species found in (1) tidepools and (2) estuaries at locations adjacent to park lands on Mount Desert Island and the Schoodic Peninsula over different seasons. The inventories were not intended to be part of a long-term monitoring effort. Rather, the objective was to sample as many diverse habitats as possible in the intertidal and estuarine zones to maximize the resultant species list. Beyond these original objectives, we evaluated the data for spatial and temporal patterns and trends as well as relationships with other biological and physical characteristics of the tidepools and estuaries. For the tidepool survey, eighteen intertidal sections with multiple pools were inventoried. The majority of the tidepool sampling took place in 2001 but a few tidepools were revisited during the spring/summer period of 2002 and 2003. Each tidepool was visited once during late spring (Period 1: June 6 – June 26), twice during the summer (Period 2: July 3 – August 2 and Period 3: August 3 – September 18) and once during early fall (Period 4: September 29 – October 21).
    [Show full text]
  • "Structure, Function and Evolution of the Nematode Genome"
    Structure, Function and Advanced article Evolution of The Article Contents . Introduction Nematode Genome . Main Text Online posting date: 15th February 2013 Christian Ro¨delsperger, Max Planck Institute for Developmental Biology, Tuebingen, Germany Adrian Streit, Max Planck Institute for Developmental Biology, Tuebingen, Germany Ralf J Sommer, Max Planck Institute for Developmental Biology, Tuebingen, Germany In the past few years, an increasing number of draft gen- numerous variations. In some instances, multiple alter- ome sequences of multiple free-living and parasitic native forms for particular developmental stages exist, nematodes have been published. Although nematode most notably dauer juveniles, an alternative third juvenile genomes vary in size within an order of magnitude, com- stage capable of surviving long periods of starvation and other adverse conditions. Some or all stages can be para- pared with mammalian genomes, they are all very small. sitic (Anderson, 2000; Community; Eckert et al., 2005; Nevertheless, nematodes possess only marginally fewer Riddle et al., 1997). The minimal generation times and the genes than mammals do. Nematode genomes are very life expectancies vary greatly among nematodes and range compact and therefore form a highly attractive system for from a few days to several years. comparative studies of genome structure and evolution. Among the nematodes, numerous parasites of plants and Strikingly, approximately one-third of the genes in every animals, including man are of great medical and economic sequenced nematode genome has no recognisable importance (Lee, 2002). From phylogenetic analyses, it can homologues outside their genus. One observes high rates be concluded that parasitic life styles evolved at least seven of gene losses and gains, among them numerous examples times independently within the nematodes (four times with of gene acquisition by horizontal gene transfer.
    [Show full text]
  • Responses of Invertebrates to Temperature and Water Stress A
    Author's Accepted Manuscript Responses of invertebrates to temperature and water stress: A polar perspective M.J. Everatt, P. Convey, J.S. Bale, M.R. Worland, S.A.L. Hayward www.elsevier.com/locate/jtherbio PII: S0306-4565(14)00071-0 DOI: http://dx.doi.org/10.1016/j.jtherbio.2014.05.004 Reference: TB1522 To appear in: Journal of Thermal Biology Received date: 21 August 2013 Revised date: 22 January 2014 Accepted date: 22 January 2014 Cite this article as: M.J. Everatt, P. Convey, J.S. Bale, M.R. Worland, S.A.L. Hayward, Responses of invertebrates to temperature and water stress: A polar perspective, Journal of Thermal Biology, http://dx.doi.org/10.1016/j.jther- bio.2014.05.004 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting galley proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. 1 Responses of invertebrates to temperature and water 2 stress: A polar perspective 3 M. J. Everatta, P. Conveyb, c, d, J. S. Balea, M. R. Worlandb and S. A. L. 4 Haywarda* a 5 School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK b 6 British Antarctic Survey, Natural Environment Research Council, High Cross, Madingley Road, 7 Cambridge, CB3 0ET, UK 8 cNational Antarctic Research Center, IPS Building, University Malaya, 50603 Kuala Lumpur, 9 Malaysia 10 dGateway Antarctica, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand 11 12 *Corresponding author.
    [Show full text]
  • Phylogeny of Tortricidae (Lepidoptera): a Morphological Approach with Enhanced Whole
    Template B v3.0 (beta): Created by J. Nail 06/2015 Phylogeny of Tortricidae (Lepidoptera): A morphological approach with enhanced whole mount staining techniques By TITLE PAGE Christi M. Jaeger AThesis Submitted to the Faculty of Mississippi State University in Partial Fulfillment of the Requirements for the Degree of Master of Science in Agriculture and Life Sciences (Entomology) in the Department of Biochemistry, Molecular Biology, Entomology, & Plant Pathology Mississippi State, Mississippi August 2017 Copyright by COPYRIGHT PAGE Christi M. Jaeger 2017 Phylogeny of Tortricidae (Lepidoptera): A morphological approach with enhanced whole mount staining techniques By APPROVAL PAGE Christi M. Jaeger Approved: ___________________________________ Richard L. Brown (Major Professor) ___________________________________ Gerald T. Baker (Committee Member) ___________________________________ Diana C. Outlaw (Committee Member) ___________________________________ Jerome Goddard (Committee Member) ___________________________________ Kenneth O. Willeford (Graduate Coordinator) ___________________________________ George M. Hopper Dean College of Agriculture and Life Sciences Name: Christi M. Jaeger ABSTRACT Date of Degree: August 11, 2017 Institution: Mississippi State University Major Field: Agriculture and Life Sciences (Entomology) Major Professor: Dr. Richard L. Brown Title of Study: Phylogeny of Tortricidae (Lepidoptera): A morphological approach with enhanced whole mount staining techniques Pages in Study 117 Candidate for Degree of Master of
    [Show full text]