Protistology Culture Collection of Parasitic Protists at the Zoological

Total Page:16

File Type:pdf, Size:1020Kb

Protistology Culture Collection of Parasitic Protists at the Zoological Protistology 10 (1), 26–42 (2016) Protistology Culture collection of parasitic protists at the Zoological Institute RAS (CCPP ZIN RAS) Marina N. Malysheva1, Maria A. Mamkaeva2, Alexei Yu. Kostygov1,3, Alexander O. Frolov1 and Sergey A. Karpov1,2 1 Zoological Institute, Russian Academy of Sciences, St. Petersburg, Russia 2 St. Petersburg State University, St. Petersburg, Russia 3 Life Science Research Centre, Faculty of Science, University of Ostrava, Ostrava, Czech Republic Summary Establishment of the bank of living cultures of trypanosomatids at the Laboratory of Protozoology, Zoological Institute of the Russian Academy of Sciences, St. Petersbug, started in 1979. The first edition of the collection catalogue (Malysheva et al., 2001) included 33 strains of trypanosomatids. The present, second edition contains descriptions of 52 strains of trypanosomatids and 28 strains of aphelids and parasitic chytridiomycetes. The strains of aphelids and parasitic chytridiomycetes were isolated and initially cultivated at the Center for Culturing Collection of Microorganisms of the Research park of St. Petersburg State University. This collection is named the Culture Collection of Parasitic Protists of the Zoological Institute RAS (CCPP ZIN RAS). Key words: Aphelididae, bibliography, culture collection, GenBank, Gromochytri- aceae, living cultures, Mesochytriaceae, parasitic protists, Trypanosomatidae Introduction depositarium of parasitic protozoans was established at the Laboratory of Protozoology of the Zoological Study of biodiversity of parasitic protists is Institute RAS in 1979. The first edition of the one of the “hot spots” in modern biology. Many collection catalogue was published in 2001 and of these organisms cause dangerous infections of included 33 strains of trypanosomatids (Malysheva humans, animals and plants, and their genetic et al., 2001). The present, second edition contains peculiarities are the unique examples of evolutionary descriptions of 52 strains of trypanosomatids changes in eukaryotes. The establishment, support augmented with 28 strains of aphelids and parasitic and accession of such culture collections are chytridiomycetes. The structure of the catalogue is very important tasks for study of biodiversity, generally the same as in the first edition (Malysheva cell biology, and parasite-host interactions. A et al., 2001); however, it was modified in two aspects: © 2016 The Author(s) Protistology © 2016 Protozoological Society Affiliated with RAS Protistology · 27 1) the deposition GenBank Numbers were included, Host: Ornidia obesa (Fabricius, 1775) (Diptera). and 2) a new section “List of the lost strains” was GenBank: AF038023, AF038026, EU079130, added. EU095978, HM593012 Bibliography: Fiorini et al., 1989; Faria e Silva Cultivating methods et al., 1991; Hollar et al., 1998; Yurchenko et al., 2009, Teixeira et al., 2011. Axenic trypanosomatid cultures have been maintained in the liquid nutrient medium BHI Genus Crithidia Léger, 1902 (Difco) with addition of hemin (25 mg/ml) and C. brevicula Frolov et Malysheva, 1989 inoculated once a month. The cultures were placed Synonyms: Crithidia allae Frolov et Malysheva, in the fridge (5° C) after inoculation and subsequent 1989 (NBrA); Wallaceina brevicula Frolov et incubation during three days at 25° C. Malysheva, 1989 (NBr, NBrB); Wallaceina incons- For cultivation of the Blastocrithidia flagellates, tans Podlipaev, Frolov et Kolesnikov, 1990 (GK); a two-phase medium has been used: the blood agar as Wallaceina vicina Malysheva et Frolov, 2004 (WG); a dense phase, and a BHI medium with the addition Leptomonas peterhoffi Podlipaev, 1985 (in part) of serum (5-10%) as a liquid phase. For cultivation (101); Wallaceina podlipaevi Malysheva et Frolov, of the Trypanosoma flagellates, a slightly modified 2009 (101); Blastocrithidia gerricola Podlipaev, 1985 two-phase medium has been used: the blood agar as (in part) (KV1); Blastocrithidia miridarum Podlipaev a dense phase, and a physiological solution with the et Frolov, 1987 (in part) (BM33); Leptomonas addition of serum (5-10%) as a liquid phase. sp. (F2); Leptomonas sp. (F5); Leptomonas sp. Accumulating cultures of the aphelids and (F6); Leptomonas sp. (F7); Leptomonas sp. (F8); chytrids were maintained in culture on Tribonema Leptomonas sp. (CL8). gayanum Pasch. (strain 20 CALU) as the host 2 Strain NBr cultivated in the mineral medium: K2HPO4 (66.7 Depositor: A.O. Frolov mg/l); MgSO4 × 7H2O (33 mg/l); KNO3 (100 History: 1986, isolated by A.O. Frolov in the mg/l); microelements (1 mg/l) of stock solution: vicinity of the Lyady village, Pskov Province, Russia. ZnSO4 × 7H2O (0.22 g/l), MgSO4 (1.81 g/l), CuSO4 Host: Nabis (Nabis) brevis Scholtz, 1847 (Hete- × 5H2O (0.079 g/l), NaBO3 × 4H2O (2.63 mg/l), roptera: Nabidae). (NH4)6Mo7O2 × 4H2O (1 mg/l), FeSO4 × 7H2O (9.3 GenBank: AF153045, AF316620, AJ401357, mg/l), CaCl2 (1.2 mg/l), Co(NO3)2 × H2O (0.02 AJ401378, EU088277- EU088279, KJ443335- mg/l), EDTA (10 mg/l), pH 7.0-7.2 (Gromov and KJ443337, KJ443350, KJ474892- KJ474894, Titova, 1991) in the 12 ml glass tubes containing KJ474931, KJ474932, Z32854, 3-5 ml of the medium at room temperature in Bibliography: Frolov and Malysheva, 1989a, the presence of light (24 h). The inoculation was 1989b; 1990; Podlipaev et al., 1991; Malysheva and performed twice a month. Frolov, 1995; Podlipaev et al., 1998; Podlipaev and Frolov, 2000; Yurchenko et al., 2000; Merzlyak Catalogue of living cultures et al., 2001a, 2001b; Yurchenko et al., 2006; Yurchenko et al., 2009; Kostygov et al., 2014 Class Kinetoplastea Honigberg 1963 emend. 3 Strain NBrB Vickerman 1976 Depositor: A.O. Frolov Subclass Metakinetoplastina Vickerman 2004 History: Clonal culture. 1986, isolated from Order Trypanosomatida Kent 1880 stat. nov. the culture of C. brevicula (NBr) in the Laboratory Hollande 1952 of Protozoology ZIN RAS, St. Petersburg, Russia. Family Trypanosomatidae Doflein 1951 Host: Nabis (Nabis) brevis Scholtz, 1847 (Hete- Genus Angomonas Souza and Corte-Real, 1991 roptera: Nabidae). A. deanei (Carvalho, 1973) Bibliography: Frolov and Malysheva, 1989a, Synonyms: Crithidia deanei Carvalho, 1973; 1989b; Kolesnikov et al., 1990; Skarlato et al., 1990; Crithidia roitmani, Fiorini et al., 1989; Herpetomonas Podlipaev et al., 1991; Malysheva and Frolov, 1995. roitmani (Fiorini et al., 1989) 4 Strain WG 1 Strain TCC080E (=ATCC 50305) Depositor: M.N. Malysheva Depositor: S.A. Podlipaev History: 2000, isolated by M.N. Malysheva in History: 1990, received from E.P. Camargo, São Komarovo, Leningrad Province, Russia. Paulo University, Brazil. Isolated in Brazil. Host: Limnoporus rufoscutellatus (Latreille, 28 · Marina N. Malysheva et al. 1807) (Heteroptera: Gerridae). Host: Nabis (Nabicula) flavomarginatus Scholtz, GenBank: KJ443338-KJ443340, KJ443354, 1847 (Heteroptera: Nabidae). KJ474895-KJ474897, KJ474907-KJ474909 GenBank: AF375664, DQ140170, KJ443317- Bibliography: Kostygov et al., 2004; Malysheva KJ443319, KJ443344, KJ474874-KJ474876, and Frolov, 2004; Kostygov et al., 2014. KJ474913-KJ474915, 5 Strain 101 Bibliography: Podlipaev and Rokitskaya, 1999; Depositor: S.A. Podlipaev Kostygov et al., 2004; Yurchenko et al., 2006; History: 1980, isolated by S.A. Podlipaev in Kostygov et al., 2014. Peterhof, St. Petersburg, Russia. 9 Strain F5 Host: Nabis (Nabicula) flavomarginatus Scholtz, Depositor: S.A. Podlipaev 1847 (Heteroptera: Nabidae). History: 1986, isolated by S.A. Podlipaev at the GenBank: JN944133, AF153039, AF322390, Cape Kartesh (White Sea), Karelia, Russia. EU088283-EU088285, KJ443308-KJ443311, Host: Nabis (Nabicula) flavomarginatus Scholtz, KJ474867, KJ474935-KJ474937, KJ443306, 1847 (Heteroptera: Nabidae). KJ443307, KJ474866, KJ474933, KJ474934 GenBank: AY547460, KJ443320-KJ443322, Bibliography: Podlipaev, 1985; Kolesnikov et KJ443345, KJ474877-KJ474879, KJ474923, al., 1990; Marakhova et al., 1991; Podlipaev et al., KJ474924 1991; Podlipaev et al., 1998; Podlipaev and Frolov, Bibliography: Podlipaev et al., 1991; Podlipaev 2000; Merzlyak et al., 2001a; Kostygov et al., 2004; and Rokitskaya, 1999; Kostygov et al., 2004; Yurchenko et al., 2006; Malysheva and Frolov, Podlipaev et al., 2004; Kostygov et al., 2014. 2009; Yurchenko et al., 2009; Gerasimov et al., 10 Strain F7 2012a; Kostygov et al., 2014. Depositor: S.A. Podlipaev 6 Strain KV1 History: 1986, isolated by S.A. Podlipaev at the Synonyms: Blastocrithidia gerricola Podlipaev, Cape Kartesh (White Sea), Karelia, Russia. 1985 (in part). Host: Nabis (Nabicula) flavomarginatus Scholtz, Depositor: S.A. Podlipaev 1847 (Heteroptera: Nabidae). History: 1981, isolated by S.A. Podlipaev at the GenBank: KJ443326-KJ443328, KJ443347, Curonian Spit, Kaliningrad Province, Russia. KJ474883-KJ474885, KJ474910-KJ474912 Host: Gerris lacustris (Linnaeus, 1758) (Hete- Bibliography: Kostygov et al., 2004; Kostygov roptera). et al., 2014. GenBank: AF153036, AF322391, AJ401379, 11 Strain CL8 AY547459; KJ443332-KJ443334, KJ443351, Depositor: A.O. Frolov KJ474889-KJ474891, KJ474928-KJ474930. History: 1984, isolated by A.O. Frolov in Bibliography: Podlipaev, 1985; Kolesnikov et Peterhof, St. Petersburg, Russia. al., 1990; Podlipaev et al., 1991; Podlipaev et al., Host: Nabis (Dolichonabis) limbatus Dahlbom, 1998; Podlipaev and Frolov, 2000; Merzlyak et al., 1851 (Heteroptera: Nabidae). 2001a, 2001b; Podlipaev et al., 2004; Yurchenko et GenBank: KJ443314-KJ443316, KJ443349, al., 2006; Kostygov et al., 2014. KJ474871-KJ474873, KJ474925-KJ474927 7 Strain BM33 Bibliography: Podlipaev and Rokitskaya, 1999; Depositor: A.O.
Recommended publications
  • Insecta Zeitschrift Für Entomologie Und Naturschutz
    Insecta Zeitschrift für Entomologie und Naturschutz Heft 9/2004 Insecta Bundesfachausschuss Entomologie Zeitschrift für Entomologie und Naturschutz Heft 9/2004 Impressum © 2005 NABU – Naturschutzbund Deutschland e.V. Herausgeber: NABU-Bundesfachausschuss Entomologie Schriftleiter: Dr. JÜRGEN DECKERT Museum für Naturkunde der Humbolt-Universität zu Berlin Institut für Systematische Zoologie Invalidenstraße 43 10115 Berlin E-Mail: [email protected] Redaktion: Dr. JÜRGEN DECKERT, Berlin Dr. REINHARD GAEDIKE, Eberswalde JOACHIM SCHULZE, Berlin Verlag: NABU Postanschrift: NABU, 53223 Bonn Telefon: 0228.40 36-0 Telefax: 0228.40 36-200 E-Mail: [email protected] Internet: www.NABU.de Titelbild: Die Kastanienminiermotte Cameraria ohridella (Foto: J. DECKERT) siehe Beitrag ab Seite 9. Gesamtherstellung: Satz- und Druckprojekte TEXTART Verlag, ERIK PIECK, Postfach 42 03 11, 42403 Solingen; Wolfsfeld 12, 42659 Solingen, Telefon 0212.43343 E-Mail: [email protected] Insecta erscheint in etwa jährlichen Abständen ISSN 1431-9721 Insecta, Heft 9, 2004 Inhalt Vorwort . .5 SCHULZE, W. „Nachbar Natur – Insekten im Siedlungsbereich des Menschen“ Workshop des BFA Entomologie in Greifswald (11.-13. April 2003) . .7 HOFFMANN, H.-J. Insekten als Neozoen in der Stadt . .9 FLÜGEL, H.-J. Bienen in der Großstadt . .21 SPRICK, P. Zum vermeintlichen Nutzen von Insektenkillerlampen . .27 MARTSCHEI, T. Wanzen (Heteroptera) als Indikatoren des Lebensraumtyps Trockenheide in unterschiedlichen Altersphasen am Beispiel der „Retzower Heide“ (Brandenburg) . .35 MARTSCHEI, T., Checkliste der bis jetzt bekannten Wanzenarten H. D. ENGELMANN Mecklenburg-Vorpommerns . .49 DECKERT, J. Zum Vorkommen von Oxycareninae (Heteroptera, Lygaeidae) in Berlin und Brandenburg . .67 LEHMANN, U. Die Bedeutung alter Funddaten für die aktuelle Naturschutzpraxis, insbesondere für das FFH-Monitoring .
    [Show full text]
  • For Review Only 377 Algomyces Stechlinensis Clustered Together with Environmental Clones from a Eutrophic 378 Lake in France (Jobard Et Al
    Journal of Eukaryotic Microbiology Page 18 of 43 1 Running head: Parasitic chytrids of volvocacean algae. 2 3 Title: Diversity and Hidden Host Specificity of Chytrids infecting Colonial 4 Volvocacean Algae. 5 Authors: Silke Van den Wyngaerta, Keilor Rojas-Jimeneza,b, Kensuke Setoc, Maiko Kagamic, 6 Hans-Peter Grossarta,d 7 a Department of ExperimentalFor Limnology, Review Leibniz-Institute Only of Freshwater Ecology and Inland 8 Fisheries, Alte Fischerhuette 2, D-16775 Stechlin, Germany 9 b Universidad Latina de Costa Rica, Campus San Pedro, Apdo. 10138-1000, San Jose, Costa Rica 10 c Department of Environmental Sciences, Faculty of Science, Toho University, Funabashi, Chiba, 11 Japan 12 d Institute of Biochemistry and Biology, Potsdam University, Maulbeerallee 2, 14476 Potsdam, 13 Germany 14 15 Corresponding Author: 16 Silke Van den Wyngaert, Department of Experimental Limnology, Leibniz-Institute of 17 Freshwater Ecology and Inland Fisheries, Alte Fischerhuette 2, D-16775 Stechlin, Germany 18 Telephone number: +49 33082 69972; Fax number: +49 33082 69917; e-mail: [email protected], 19 [email protected] 20 21 22 23 1 Page 19 of 43 Journal of Eukaryotic Microbiology 24 ABSTRACT 25 Chytrids are zoosporic fungi that play an important, but yet understudied, ecological role in 26 aquatic ecosystems. Many chytrid species have been morphologically described as parasites on 27 phytoplankton. However, the majority of them have rarely been isolated and lack DNA sequence 28 data. In this study we isolated and cultivated three parasitic chytrids, infecting a common 29 volvocacean host species, Yamagishiella unicocca. In order to identify the chytrids, we 30 characterized morphology and life cycle, and analyzed phylogenetic relationships based on 18S 31 and 28S rDNA genes.
    [Show full text]
  • Insects That Feed on Trees and Shrubs
    INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture,
    [Show full text]
  • Boxelder Bug
    BOXELDER BUG Integrated Pest Management for Home Gardeners and Landscape Professionals The western boxelder bug (Boisea rubrolineata) is often a nuisance pest around and in homes. Boxelder bugs usually feed on the leaves, flowers, and seedpods of the female or seedbearing box elder tree (Acer negundo), although they may also subsist on male box elder trees and occasionally occur on maple and ash trees. They may feed on the fruits of almond, apple, cherry, peach, Figure 1. Boxelder bug adult and nymphs. Figure 2. Young nymph of western box- pear, and plum trees, and on grapes, (J. K. Clark) elder bug, Boisea rubrolineata. where their feeding punctures cause (J. K. Clark) the fruit to become deformed. Large numbers of the bug usually occur only on female box elder trees. IDENTIFICATION When full grown, the boxelder bug is about 1/2 inch long and one-third as wide. Adults are mostly black and have three red lines on the pronotum of the thorax (one down the middle and on each margin) and several fine Figure 3. Boxelder bug eggs on leaf. Figure 4. Adult squash bug. red lines on each wing (Figure 1). The (J. K. Clark) (J. K. Clark) wings lie flat on the bug’s back when it is at rest. The abdomen is red. The young nymphs are bright red (Figure 2) and when approaching adulthood, become marked with black and begin to develop black wing pads. Eggs are yellow when first laid but become red as nymphs develop inside (Figure 3). Boxelder bugs are true bugs (Order: Hemiptera) in the family Rhopalidae.
    [Show full text]
  • Boxelder Bug Nuisance Management for Homeowners
    CIS 1155 Boxelder Bug Nuisance Management for Homeowners by Danielle Gunn and Edward John Bechinski Boxelder bugs are a common nuisance pest in Figure 1. Idaho homes and yards. Although not particu- Comparative larly harmful, these insects can be aggravating life-size boxelder when they are searching for places to spend the bug 1st-stage winter. nymph (left) and adult (right). This publication will help you understand both the seasonal biology of boxelder bugs in Idaho, and landscape features that increase pest prob- lems. We discuss the relative importance of these insects as pests. Practical steps you can take to reduce nuisance problems include alternatives to insecticides and safe, effective insecticide use. Identification Boxelder bugs develop through three life stages: eggs, nymphs, and adults. Figure 1 shows the actual body sizes of a newly hatched nymph and a mature adult. Adults are the most commonly encountered life Figure 2. Adult boxelder bugs, Boisea trivittata, are stage. Adult boxelder bugs are flattened, elon- distinctively marked with red lines on a slate-gray back- gate insects approximately one-half-inch long ground. (not including antennae). Overall upper body color is slate gray to black. Reddish orange lines appear behind the head and along the sides of the body (Figure 2). The rest of the body under the wings is red with two rows of black spots. Legs and antennae are black. Eggs. Small red eggs occur in clusters on box- elder and maple trees. Elongate eggs one-six- teenth-inch long are laid in groups of about ten on the bark and leaves of host trees and sur- rounding areas.
    [Show full text]
  • Morphological, Molecular, and Ultrastructural Characterization of Rozella Rhizoclosmatii, a New Species in Cryptomycota
    fungal biology 121 (2017) 1e10 journal homepage: www.elsevier.com/locate/funbio Morphological, molecular, and ultrastructural characterization of Rozella rhizoclosmatii, a new species in Cryptomycota Peter M. LETCHERa,*, Joyce E. LONGCOREb, C. Alisha QUANDTc, Domingos da Silva LEITEd, Timothy Y. JAMESc, Martha J. POWELLa aDepartment of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA bSchool of Biology and Ecology, University of Maine, Orono, ME 04469, USA cDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA dDepartamento de Genetica, Evoluc¸ao~ e Bioagentes, Universidade Estadual de Campinas, Campinas, SP, 13082-862, Brazil article info abstract Article history: Rozella is a genus of unwalled endoparasites of a variety of hosts including Oomycota (Stra- Received 10 June 2016 menopiles), Blastocladiomycota and Chytridiomycota (Fungi), and one green alga (Coleo- Received in revised form chaete, Chlorophyceae). It currently includes more than 20 formally described species, 15 August 2016 and no new species of Rozella have been described since 1987. We discovered a new Rozella Accepted 19 August 2016 species parasitizing Rhizoclosmatium globosum (Chytridiales, Chytridiomycota) and investi- Available online 4 September 2016 gated its morphology, ultrastructure, and phylogenetic position. Herein named as Rozella Corresponding Editor: rhizoclosmatii sp. nov., the organism induces hypertrophy of the host. Its zoospore is ultra- Gordon William Beakes structurally similar to that of Rozella allomycis, although it has a unique zoospore ultrastruc- tural feature, a lattice of perpendicular rods about the nucleus. The 18S rDNA molecular Keywords: sequence of R. rhizoclosmatii is similar to that of the previously sequenced ‘Rozella ex Rhizo- Lattice closmatium’. This is the first study to inclusively characterize a new species of Rozella with Morphology morphological, ultrastructural and molecular data.
    [Show full text]
  • A Higher-Level Phylogenetic Classification of the Fungi
    mycological research 111 (2007) 509–547 available at www.sciencedirect.com journal homepage: www.elsevier.com/locate/mycres A higher-level phylogenetic classification of the Fungi David S. HIBBETTa,*, Manfred BINDERa, Joseph F. BISCHOFFb, Meredith BLACKWELLc, Paul F. CANNONd, Ove E. ERIKSSONe, Sabine HUHNDORFf, Timothy JAMESg, Paul M. KIRKd, Robert LU¨ CKINGf, H. THORSTEN LUMBSCHf, Franc¸ois LUTZONIg, P. Brandon MATHENYa, David J. MCLAUGHLINh, Martha J. POWELLi, Scott REDHEAD j, Conrad L. SCHOCHk, Joseph W. SPATAFORAk, Joost A. STALPERSl, Rytas VILGALYSg, M. Catherine AIMEm, Andre´ APTROOTn, Robert BAUERo, Dominik BEGEROWp, Gerald L. BENNYq, Lisa A. CASTLEBURYm, Pedro W. CROUSl, Yu-Cheng DAIr, Walter GAMSl, David M. GEISERs, Gareth W. GRIFFITHt,Ce´cile GUEIDANg, David L. HAWKSWORTHu, Geir HESTMARKv, Kentaro HOSAKAw, Richard A. HUMBERx, Kevin D. HYDEy, Joseph E. IRONSIDEt, Urmas KO˜ LJALGz, Cletus P. KURTZMANaa, Karl-Henrik LARSSONab, Robert LICHTWARDTac, Joyce LONGCOREad, Jolanta MIA˛ DLIKOWSKAg, Andrew MILLERae, Jean-Marc MONCALVOaf, Sharon MOZLEY-STANDRIDGEag, Franz OBERWINKLERo, Erast PARMASTOah, Vale´rie REEBg, Jack D. ROGERSai, Claude ROUXaj, Leif RYVARDENak, Jose´ Paulo SAMPAIOal, Arthur SCHU¨ ßLERam, Junta SUGIYAMAan, R. Greg THORNao, Leif TIBELLap, Wendy A. UNTEREINERaq, Christopher WALKERar, Zheng WANGa, Alex WEIRas, Michael WEISSo, Merlin M. WHITEat, Katarina WINKAe, Yi-Jian YAOau, Ning ZHANGav aBiology Department, Clark University, Worcester, MA 01610, USA bNational Library of Medicine, National Center for Biotechnology Information,
    [Show full text]
  • (HEMIPTERA: HETEROPTERA) NA POBRZEŻU BAŁTYKU New Data On
    Przegląd Przyrodniczy XXIX, 1 (2018): 41-57 Grzegorz Gierlasiński, Karol Szawaryn, Grzegorz Hebda, Tomasz Rutkowski NOWE DANE O WYSTĘPOWANIU LĄDOWYCH PLUSKWIAKÓW RÓŻNOSKRZYDŁYCH (HEMIPTERA: HETEROPTERA) NA POBRZEŻU BAŁTYKU New data on the occurrence of terrestrial true-bugs (Hemiptera: Heteroptera) from the Polish Baltic Coast ABSTRAKT: Niniejsza praca prezentuje nowe dane o występowaniu pluskwiaków różnoskrzydłych na Pobrzeżu Bałtyku. Spośród 131 gatunków zebranych z 27 różnych lokalizacji osiem jest nowych dla kra- iny: Acetropis gimmerthalii, Agramma femorale, Chartoscirta cocksi, Grypocoris sexguttatus, Hallodapus rufescens, Nithecus jacobaeae, Rhynocoris iracundus, Trapezonotus desertus. SŁOWA KLUCZOWE: Heteroptera, pluskwiaki różnoskrzydłe, Pobrzeże Bałtyku, faunistyka, nowe dane ABSTRacT: New faunistic data on the occurrence of terrestrial true-bugs in Baltic Coast are presented. In total, the paper presents the data concerning 131 species of Heteroptera collected on 27 different si- tes. Eight species: Acetropis gimmerthalii, Agramma femorale, Chartoscirta cocksi, Grypocoris sexguttatus, Hallodapus rufescens, Nithecus jacobaeae, Rhynocoris iracundus and Trapezonotus desertus are recorded for the first time from Polish Baltic Coast. KEY woRDS: Hemiptera, Heteroptera, true-bugs, faunistics, new data, first record, Baltic Coast, Po- land. Wstęp Zawirska (1998), Lis B. i Lis J.A. (2002), Korcz (2003), Łęgowski i Lis B. (2008), Tarnawski Lądowe pluskwiaki różnoskrzydłe Po- (2011, 2013), Lis B. i Kowalczyk (2017). W brzeża Bałtyku były przedmiotem badań kilku ciągu ostatnich trzydziestu lat stwierdzono badaczy niemieckich w XIX i w pierwszej po- w tej krainie 294 gatunki pluskwiaków. Ze- łowie XX wieku (Siebold 1839, Brischke 1888, stawienie kwadratów UTM, z których po- 1894, Enderlein 1908, Schmidt 1928, Karl chodzą dotychczasowe, literaturowe dane o 1935, Wagner 1941). Również w kolejnych Heteroptera Pobrzeża Bałtyku zilustrowano latach były w tym regionie prowadzone prace na rycinie 1.
    [Show full text]
  • Systematics of the Lobulomycetales, a New Order Within the Chytridiomycota David Rabern Simmons
    The University of Maine DigitalCommons@UMaine Electronic Theses and Dissertations Fogler Library 5-2007 Systematics of the Lobulomycetales, a New Order within the Chytridiomycota David Rabern Simmons Follow this and additional works at: http://digitalcommons.library.umaine.edu/etd Part of the Botany Commons Recommended Citation Simmons, David Rabern, "Systematics of the Lobulomycetales, a New Order within the Chytridiomycota" (2007). Electronic Theses and Dissertations. 671. http://digitalcommons.library.umaine.edu/etd/671 This Open-Access Dissertation is brought to you for free and open access by DigitalCommons@UMaine. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of DigitalCommons@UMaine. SYSTEMATICS OF THE LOBULOMYCETALES, A NEW ORDER WITHIN THE CHYTRIDIOMYCOTA By David Rabern Simmons B.S. University of Virginia's College at Wise, 2004 A THESIS Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science (in Botany and Plant Pathology) The Graduate School University of Maine May, 2007 Advisory Committee: Joyce E. Longcore, Research Associate Professor of Biology, Advisor Seanna L. Annis, Associate Professor of Mycology Seth Tyler, Professor of Zoology and Cooperating Professor of Marine Sciences Copyright 2007 David Rabern Simmons SYSTEMATICS OF THE LOBULOMYCETALES, A NEW ORDER WITHIN THE CHYTRIDIOMYCOTA By David Rabern Simmons Thesis Advisor: Dr. Joyce E. Longcore An Abstract of the Thesis Presented in Partial Fulfillment of the Requirements for the Degree of Master of Science (in Botany and Plant Pathology) May, 2007 Based on molecular phylogenetic analyses, the polyphyletic order Chytridiales, one of the four orders in the Chytridiomycota, contains several well- supported clades.
    [Show full text]
  • Rhizophlyctidalesda New Order in Chytridiomycota
    mycological research 112 (2008) 1031–1048 journal homepage: www.elsevier.com/locate/mycres Rhizophlyctidalesda new order in Chytridiomycota Peter M. LETCHER*, Martha J. POWELL, Donald J. S. BARR, Perry F. CHURCHILL, William S. WAKEFIELD, Kathryn T. PICARD Department of Biological Sciences, The University of Alabama, 411 Hackberry Lane, 319 Biology, Box 870344, Tuscaloosa, AL 35487, USA article info abstract Article history: Rhizophlyctis rosea (Chytridiomycota) is an apparently ubiquitous, soil-inhabiting, cellulose- Received 10 January 2008 degrading chytrid that is the type for Rhizophlyctis. Previous studies have revealed multiple Received in revised form zoospore subtypes among morphologically indistinguishable isolates in the R. rosea com- 27 February 2008 plex sensu Barr. In this study we analysed zoospore ultrastructure and combined nu- Accepted 18 March 2008 rRNA gene sequences (partial LSU and complete ITS1–5.8S–ITS2) of 49 isolates from globally Corresponding Editor: distributed soil samples. Based on molecular monophyly and zoospore ultrastructure, this Gordon W. Beakes group of Rhizophlyctis rosea-like isolates is designated as a new order, the Rhizophlyctidales. Within the Rhizophlyctidales are four new families (Rhizophlyctidaceae, Sonoraphlyctidaceae, Keywords: Arizonaphlyctidaceae, and Borealophlyctidaceae) and three new genera (Sonoraphlyctis, Arizona- Phylogeny phlyctis, and Borealophlyctis). rDNA Rhizophlyctis ª 2008 The British Mycological Society. Published by Elsevier Ltd. All rights reserved. Ultrastructure Zoospore
    [Show full text]
  • 3 Zoologische Rätsel Zur Endemitenfauna Im Nationalpark Gesäuse
    3 E NDEMITEN -R Ä T S E L I M NP GE S Ä U S E 2014 3 Zoologische Rätsel zur Endemitenfauna im Nationalpark Gesäuse Tiergruppen: Weberknechte, Wanzen & Zikaden Inkl. Arbeitsnachweis: Landschneckenfauna des NPs Gesäuse Auftraggeber: Nationalpark Gesäuse GmbH Endbericht: Spinnentiere& Insekten Graz, im Dez. 2014 3 E NDEMITEN -R Ä T S E L I M NP GE S Ä U S E 2014 ÖKOTEAM – Institut für Tierökologie und Naturraumplanung OG Ingenieurbüro für Biologie A - 8010 Graz, Bergmanngasse 22 Tel.: 0316/35 16 50 Fax DW 4 e-mail: [email protected] 3 Zoologische Rätsel zur Endemitenfauna im Nationalpark Gesäuse Tiergruppen: Weberknechte, Wanzen & Zikaden Inklusive Arbeitsnachweis: Landschneckenfauna des Nationalparks Gesäuse Endbericht 2014 Version 02 Auftraggeber: Fachbearbeitungen: Nationalpark Gesäuse GmbH Mag. Dr. Thomas FRIEß Leitung Fachbereich Naturschutz/Naturraum PD Mag. Dr. Werner HOLZINGER Mag. MSc. Daniel Kreiner Mag. Dr. Christian KOMPOSCH 8913 Weng im Gesäuse 2 Mag. Lydia SCHLOSSER Technische AssistentInnen: Sandra AURENHAMMER MSc. Mag. Brigitte KOMPOSCH MSc. Mag. Julia SCHWAB Lektorat: Astrid LEITNER Auftragnehmer: Mag. Daniel KREINER MSc. ÖKOTEAM – Institut für Tierökologie und Naturraumplanung OG Projektleitung: Mag. Dr. Christian KOMPOSCH Zitiervorschlag: ÖKOTEAM – KOMPOSCH Ch., T. FRIEß, W. HOLZINGER & L. SCHLOSSER (2014): 3 Zoologische Rätsel zur Endemitenfauna im Nationalpark Gesäuse. Tiergruppen: Weberknechte, Wanzen & Zikaden. – Unveröffentlichter Projektbericht im Auftrag der Nationalpark Gesäuse GmbH, 86 Seiten. Graz, am 10. Dez.
    [Show full text]
  • Clade (Kingdom Fungi, Phylum Chytridiomycota)
    TAXONOMIC STATUS OF GENERA IN THE “NOWAKOWSKIELLA” CLADE (KINGDOM FUNGI, PHYLUM CHYTRIDIOMYCOTA): PHYLOGENETIC ANALYSIS OF MOLECULAR CHARACTERS WITH A REVIEW OF DESCRIBED SPECIES by SHARON ELIZABETH MOZLEY (Under the Direction of David Porter) ABSTRACT Chytrid fungi represent the earliest group of fungi to have emerged within the Kingdom Fungi. Unfortunately despite the importance of chytrids to understanding fungal evolution, the systematics of the group is in disarray and in desperate need of revision. Funding by the NSF PEET program has provided an opportunity to revise the systematics of chytrid fungi with an initial focus on four specific clades in the order Chytridiales. The “Nowakowskiella” clade was chosen as a test group for comparing molecular methods of phylogenetic reconstruction with the more traditional morphological and developmental character system used for classification in determining generic limits for chytrid genera. Portions of the 18S and 28S nrDNA genes were sequenced for isolates identified to genus level based on morphology to seven genera in the “Nowakowskiella” clade: Allochytridium, Catenochytridium, Cladochytrium, Endochytrium, Nephrochytrium, Nowakowskiella, and Septochytrium. Bayesian, parsimony, and maximum likelihood methods of phylogenetic inference were used to produce trees based on one (18S or 28S alone) and two-gene datasets in order to see if there would be a difference depending on which optimality criterion was used and the number of genes included. In addition to the molecular analysis, taxonomic summaries of all seven genera covering all validly published species with a listing of synonyms and questionable species is provided to give a better idea of what has been described and the morphological and developmental characters used to circumscribe each genus.
    [Show full text]