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University of Copenhagen, 1353 Copenhagen, Denmark
Molecular phylogeny of Edraianthus (Grassy Bells; Campanulaceae) based on non- coding plastid DNA sequences Stefanovic, Sasa; Lakusic, Dmitar; Kuzmina, Maria; Mededovic, Safer; Tan, Kit; Stevanovic, Vladimir Published in: Taxon Publication date: 2008 Document version Publisher's PDF, also known as Version of record Citation for published version (APA): Stefanovic, S., Lakusic, D., Kuzmina, M., Mededovic, S., Tan, K., & Stevanovic, V. (2008). Molecular phylogeny of Edraianthus (Grassy Bells; Campanulaceae) based on non-coding plastid DNA sequences. Taxon, 57(2), 452-475. Download date: 02. okt.. 2021 Stefanović & al. • Phylogeny of Edraianthus TAXON 57 (2) • May 2008: 452–475 Molecular phylogeny of Edraianthus (Grassy Bells; Campanulaceae) based on non-coding plastid DNA sequences Saša Stefanović1*, Dmitar Lakušić2, Maria Kuzmina1, Safer Međedović3, Kit Tan4 & Vladimir Stevanović2 1 Department of Biology, University of Toronto at Mississauga, Mississauga, Ontario L5L 1C6, Canada. *[email protected] (author for correspondence) 2 Institute of Botany and Botanical Garden “Jevremovac”, Faculty of Biology, University of Belgrade, 11000 Belgrade, Serbia 3 University of Sarajevo, Faculty of Forestry, 71000 Sarajevo, Bosnia and Herzegovina 4 Institute of Biology, University of Copenhagen, 1353 Copenhagen, Denmark The Balkan Peninsula is known as an ice-age refugium and an area with high rates of speciation and diversifi- cation. Only a few genera have their centers of distribution in the Balkans and the endemic genus Edraianthus is one of its most prominent groups. As such, Edraianthus is an excellent model not only for studying specia- tion processes and genetic diversity but also for testing hypotheses regarding biogeography, identification and characterization of refugia, as well as post-glacial colonization and migration dynamics in SE Europe. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Coleoptera: Coccinellidae): Influence of Subelytral Ultrastructure
Experimental & Applied Acarology, 23 (1999) 97–118 Review Phoresy by Hemisarcoptes (Acari: Hemisarcoptidae) on Chilocorus (Coleoptera: Coccinellidae): influence of subelytral ultrastructure M.A. Houck* Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409–3131, USA (Received 9 January 1997; accepted 17 April 1998) ABSTRACT The non-phoretic stages of mites of the genus Hemisarcoptes are predators of the family Diaspididae. The heteromorphic deutonymph (hypopus) maintains a stenoxenic relationship with beetles of the genus Chilocorus. The mites attach to the subelytral surface of the beetle elytron during transport. There is variation in mite density among species of Chilocorus. Both Hemisarcoptes and Chilocorus have been applied to biological control programmes around the world. The objective of this study was to determine whether subelytral ultrastructure (spine density) plays a role in the evolution of symbiosis between the mite and the beetle. The subelytral surfaces of 19 species of Chilocorus and 16 species of Exochomus were examined. Spine density was determined for five subelytral zones: the anterior pronotal margin, medial central region, caudoventral tip, lateral distal margin and epipleural region. Spine density on the subelytral surface of Chilocorus and Exochomus was inversely correlated with the size of the elytron for all zones except the caudoventral tip. This suggests that an increase in body size resulted in a redistribution of spines and not an addition of spines. The pattern of spine density in Exochomus and Chilocorus follows a single size–density trajectory. The pattern of subelytral ultrastructure is not strictly consistent with either beetle phylogeny or beetle allometry. The absence of spines is not correlated with either beetle genus or size and species of either Chilocorus or Exochomus may be devoid of spines in any zone, irrespective of body size. -
Evaluating a Standardized Protocol and Scale for Determining Non-Native Insect Impact
A peer-reviewed open-access journal NeoBiota 55: 61–83 (2020) Expert assessment of non-native insect impacts 61 doi: 10.3897/neobiota.55.38981 RESEARCH ARTICLE NeoBiota http://neobiota.pensoft.net Advancing research on alien species and biological invasions The impact is in the details: evaluating a standardized protocol and scale for determining non-native insect impact Ashley N. Schulz1, Angela M. Mech2, 15, Craig R. Allen3, Matthew P. Ayres4, Kamal J.K. Gandhi5, Jessica Gurevitch6, Nathan P. Havill7, Daniel A. Herms8, Ruth A. Hufbauer9, Andrew M. Liebhold10, 11, Kenneth F. Raffa12, Michael J. Raupp13, Kathryn A. Thomas14, Patrick C. Tobin2, Travis D. Marsico1 1 Arkansas State University, Department of Biological Sciences, PO Box 599, State University, AR 72467, USA 2 University of Washington, School of Environmental and Forest Sciences, 123 Anderson Hall, 3715 W Stevens Way NE, Seattle, WA 98195, USA 3 U.S. Geological Survey, Nebraska Cooperative Fish and Wildlife Unit, University of Nebraska-Lincoln, 423 Hardin Hall, 3310 Holdrege Street, Lincoln, NE 68583, USA 4 Dartmouth College, Department of Biological Sciences, 78 College Street, Hanover, NH 03755, USA 5 The University of Georgia, Daniel B. Warnell School of Forestry and Natural Resources, 180 E. Green St., Athens, GA 30602, USA 6 Stony Brook University, Department of Ecology and Evolution, Stony Brook, NY 11794, USA 7 USDA Forest Service Northern Research Station, 51 Mill Pond Rd., Hamden, CT 06514, USA 8 The Davey Tree Expert Company, 1500 N Mantua St., Kent, OH 44240, USA -
Coleoptera: Coccinellidae) As a Biocontrol Agent
CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources 2009 4, No. 046 Review Factors affecting utility of Chilocorus nigritus (F.) (Coleoptera: Coccinellidae) as a biocontrol agent D.J. Ponsonby* Address: Ecology Research Group, Department of Geographical and Life Sciences, Canterbury Christ Church University, North Holmes Road, Canterbury, Kent. CT1 1QU, UK. *Correspondence: Email: [email protected] Received: 30 March 2009 Accepted: 25 June 2009 doi: 10.1079/PAVSNNR20094046 The electronic version of this article is the definitive one. It is located here: http://www.cababstractsplus.org/cabreviews g CAB International 2009 (Online ISSN 1749-8848) Abstract Chilocorus nigritus (F.) has been one of the most successful coccidophagous coccinellids in the history of classical biological control. It is an effective predator of many species of Diaspididae, some Coccidae and some Asterolecaniidae, with an ability to colonize a relatively wide range of tropical and sub-tropical environments. It appears to have few natural enemies, a rapid numerical response and an excellent capacity to coexist in stable relationships with parasitoids. A great deal of literature relating to its distribution, biology, ecology, mass rearing and prey preferences exists, but there is much ambiguity and the beetle sometimes inexplicably fails to establish, even when conditions are apparently favourable. This review brings together the key research relating to factors that affect its utility in biocontrol programmes, including its use in indoor landscapes and temperate glasshouses. Data are collated and interpreted and areas where knowledge is lacking are identified. Recommendations are made for prioritizing further research and improving its use in biocontrol programmes. -
Reconstructing the History of Campanulaceae.Pdf
Molecular Phylogenetics and Evolution 52 (2009) 575–587 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Reconstructing the history of Campanulaceae with a Bayesian approach to molecular dating and dispersal–vicariance analyses Cristina Roquet a,b,*, Isabel Sanmartín c, Núria Garcia-Jacas a, Llorenç Sáez b, Alfonso Susanna a, Niklas Wikström d, Juan José Aldasoro c a Institut Botànic de Barcelona (CSIC-ICUB), Passeig del Migdia s. n., Parc de Montjuïc, E-08038 Barcelona, Catalonia, Spain b Unitat de Botànica, Facultat de Ciències, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Catalonia, Spain c Real Jardín Botánico de Madrid (CSIC), Plaza de Murillo, 2, E-28014 Madrid, Spain d Evolutionsbiologiskt centrum, University of Uppsala, Norbyvägen 18D, SE-752 36 Uppsala, Sweden article info abstract Article history: We reconstruct here the spatial and temporal evolution of the Campanula alliance in order to better Received 19 June 2008 understand its evolutionary history. To increase phylogenetic resolution among major groups (Wahlen- Revised 6 May 2009 bergieae–Campanuleae), new sequences from the rbcL region were added to the trnL-F dataset obtained Accepted 15 May 2009 in a previous study. These phylogenies were used to infer ancestral areas and divergence times in Cam- Available online 21 May 2009 panula and related genera using a Bayesian approach to molecular dating and dispersal–vicariance anal- yses that takes into account phylogenetic uncertainty. The new phylogenetic analysis confirms Keywords: Platycodoneae as the sister group of Wahlenbergieae–Campanuleae, the two last ones inter-graded into Bayes-DIVA, Molecular dating a well-supported clade. -
A New Record of the Armored Scale Genus Carulaspis Macgillivray
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 2016 A new record of the armored scale genus Carulaspis MacGillivray (Hemiptera: Diaspididae) from Korea and its aphelinid parasitoids (Hymenoptera: Aphelinidae) Soo-Jung Suh 167, Yongjeon 1-ro, Gimcheon-si Gyeongsangbuk-do, South Korea, [email protected] Gregory A. Evans USDA/Animal Plant Health Inspection Service Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons Suh, Soo-Jung and Evans, Gregory A., "A new record of the armored scale genus Carulaspis MacGillivray (Hemiptera: Diaspididae) from Korea and its aphelinid parasitoids (Hymenoptera: Aphelinidae)" (2016). Insecta Mundi. 974. http://digitalcommons.unl.edu/insectamundi/974 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 0466 A new record of the armored scale genus Carulaspis MacGillivray (Hemiptera: Diaspididae) from Korea and its aphelinid parasitoids (Hymenoptera: Aphelinidae) Soo-Jung Suh 167, Yongjeon 1-ro, Gimcheon-si Gyeongsangbuk-do, South Korea 39660 Gregory A. Evans USDA/Animal Plant Health Inspection Service 10300 Baltimore Avenue Beltsville, MD 20705 USA Date of Issue: January 22, 2016 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Soo-Jung Suh and Gregory A. Evans A new record of the armored scale genus Carulaspis MacGillivray (Hemiptera: Diaspididae) from Korea, and its aphelinid parasitoids (Hymenoptera: Aphelinidae) Insecta Mundi 0466: 1–6 ZooBank Registered: urn:lsid:zoobank.org:pub:4C0AB655-B42F-4486-9180-D76547CD6A50 Published in 2016 by Center for Systematic Entomology, Inc. -
Scale Insects of Britain
SCALE INSECTS OF BRITAIN Duncan Allen & Chris Malumphy Fera Science Ltd., National Agri-Food Innovation Campus Sand Hutton, York, UK YO41 1LZ Outline of talk • What are Scale insects? • Biology • Beneficial scales • Scale insect plant pests • Scale insects in Britain • Detection in different habitats • How to identify scales • Why study scale insects in Animal or vegetable? One Britain? species was only determined to be an insect and not a seed, following a lawsuit (Imms, 1990) What are scale insects? • Plant-sap feeding insects • Related to aphids, whitefly & psyllids • Feed on all parts of the plant • 8000 species • 1050 genera • Between 20-31 families • Higher classification is evolving https://horticulture.com.au/wp-content/uploads/2017/02/Scale-insect-pest-management- plan.pdf Biology and Dispersal • Sexually dimorphic; neotenic females; non-feeding winged adult males • Females 3-4 instars; Males 5 instars • Reproduce sexually, parthenogenetically and hermaphrodites • Most lay eggs, protected by an ovisac, female's body, separate scale-like cover, between wax plates or inside a ventral abdominal pouch • First instars (crawlers) actively disperse and carried by wind • Commonly transported in trade. One of the most successful colonising groups of insects in warmer parts of the world Scale insect life cycle • Beech felt scale Cryptococcus fagisuga • Females 4 instars; males 5 instars • Univoltine (Morales et al 1988) Beneficial scale insects • Used for centuries for production of dyes (Dactylopius, Kermes, Porphyrophora) • Lacquers (Shellac -
WRA Species Report
Family: Cupressaceae Taxon: Juniperus bermudiana Synonym: Juniperus virginiana var. bermudiana (L.) Va Common Name: Bemuda juniper Sabina bermudiana (L.) Antoine Bermuda cedar Questionaire : current 20090513 Assessor: Chuck Chimera Designation: H(HPWRA) Status: Assessor Approved Data Entry Person: Chuck Chimera WRA Score 7 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? y=1, n=-1 103 Does the species have weedy races? y=1, n=-1 201 Species suited to tropical or subtropical climate(s) - If island is primarily wet habitat, then (0-low; 1-intermediate; 2- High substitute "wet tropical" for "tropical or subtropical" high) (See Appendix 2) 202 Quality of climate match data (0-low; 1-intermediate; 2- High high) (See Appendix 2) 203 Broad climate suitability (environmental versatility) y=1, n=0 n 204 Native or naturalized in regions with tropical or subtropical climates y=1, n=0 y 205 Does the species have a history of repeated introductions outside its natural range? y=-2, ?=-1, n=0 y 301 Naturalized beyond native range y = 1*multiplier (see y Appendix 2), n= question 205 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see y Appendix 2) 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see n Appendix 2) 304 Environmental weed n=0, y = 2*multiplier (see Appendix 2) 305 Congeneric weed n=0, y = 1*multiplier (see y Appendix 2) 401 Produces spines, thorns or burrs y=1, n=0 n 402 Allelopathic y=1, n=0 403 Parasitic y=1, n=0 n 404 Unpalatable to grazing animals y=1, -
Phylogeny and Classification of Armored Scale Insects (Hemiptera: Coccomorpha: Diaspididae)
Zootaxa 4616 (1): 001–098 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2019 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4616.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:1B9DFBC9-2BA8-4619-8F70-E372DCBD7411 ZOOTAXA 4616 Phylogeny and classification of armored scale insects (Hemiptera: Coccomorpha: Diaspididae) BENJAMIN B. NORMARK1,2,7, AKIKO OKUSU1, GEOFFREY E. MORSE3, DANIEL A. PETERSON1,2,4, TAKAO ITIOKA5 & SCOTT A. SCHNEIDER1, 2, 6 1Department of Biology, University of Massachusetts, Amherst, Massachusetts, U.S.A. 2Graduate Program in Organismic and Evolutionary Biology, University of Massachusetts, Amherst, Massachusetts, U.S.A. 3Department of Biology, University of San Diego, San Diego, California, U.S.A. E-mail: [email protected] 4Present address: Finch Therapeutics, Somerville, Massachusetts, U.S.A. 5Graduate School of Human and Environmental Studies, Kyoto University, Japan. E-mail: [email protected] 6Present address: USDA, Agricultural Research Service, Henry A. Wallace Beltsville Agricultural Research Center, Systematic Ento- mology Laboratory, Beltsville, Maryland, U.S.A. E-mail: [email protected] 7Corresponding author. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by G. Watson: 5 Feb. 2019; published: 17 Jun. 2019 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 BENJAMIN B. NORMARK, AKIKO OKUSU, GEOFFREY E. MORSE, DANIEL A. PETERSON, TAKAO ITIOKA & SCOTT A. SCHNEIDER Phylogeny and classification of armored scale insects (Hemiptera: Coccomorpha: Diaspididae) (Zootaxa 4616) 98 pp.; 30 cm. 17 Jun. 2019 ISBN 978-1-77670-683-9 (paperback) ISBN 978-1-77670-684-6 (Online edition) FIRST PUBLISHED IN 2019 BY Magnolia Press P.O. -
Evaluating the Ornamental Value of the Caucasian Flora in Georgia
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Tuexenia - Mitteilungen der Floristisch-soziologischen Arbeitsgemeinschaft Jahr/Year: 2017 Band/Volume: NS_37 Autor(en)/Author(s): Beisheim Katja Artikel/Article: Evaluating the ornamental value of the Caucasian flora in Georgia 333- 354 ©Floristisch-soziologische Arbeitsgemeinschaft; www.tuexenia.de; download unter www.zobodat.at Tuexenia 37: 333–354. Göttingen 2017. doi: 10.14471/2017.37.008, available online at www.tuexenia.de Evaluating the ornamental value of the Caucasian flora in Georgia Bewertung des Zierpflanzenwertes der kaukasischen Flora in Georgien Katja Beisheim1, 2 & Annette Otte1, 3, * 1Division of Landscape Ecology and Landscape Planning, Research Centre for BioSystems, Land Use and Nutrition (IFZ), Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany; 2School of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland; 3Center for International Development and Environmental Research, Justus Liebig University Giessen, Senckenbergstrasse 3, 35390 Giessen, Germany *Corresponding author, e-mail: [email protected] Abstract The flora in the Caucasus Ecoregion is rich in economically important plants. While its value in terms of food crops and medicinal plants has recently been subject to scientific research, the ornamental value of many Caucasian plant species has not yet been fully recognized. In order to assess the orna- mental value of the Caucasian flora, vegetation data from two mountainous study regions in Georgia (n = 958 species, mostly grassland vegetation) was compared with the product range of ornamental plants in Germany using an online plant shopping guide. Characterization of the 150 plant species listed in both databases revealed that 121 species are present in central Europe and 117 species are natives or archaeophytes in Germany. -
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REDIA, XCIX, 2016: 163-170 http://dx.doi.org/10.19263/REDIA-99.16.21 ÖZLEM DOSTBİL (*) - SELMA ÜLGENTÜRK (**) BIO-ECOLOGY OF CEDAR SCALE INSECT TOROSASPIS CEDRICOLA (BALACHOWSKY & ALKAN) (HEMIPTERA DIASPIDIDAE) IN ANKARA, TURKEY (1) (*) Ministry of Forestry and Water Affairs, General Directorate of Forestry, Central Anatolia Forestry Research Institute, Ankara, Turkey (**) Ankara University Faculty of Agriculture, Department of Plant Protection, 06110 Dışkapı, Ankara, Turkey; e-mail: [email protected] Dostbil Ö., Ülgentürk S. – Bio-ecology of cedar scale insect Torosaspis cedricola (Balachowsky & Alkan) (Hemiptera Diaspididae) in Ankara, Turkey. Lebanon cedar, Cedrus libani A. Rich. (Pinaceae) is a significant tree from the historical, cultural, aesthetic, scientific and economic perspectives. It is presently found primarily in the Taurus Mountains with extensive and magnificent forests. Also, it has been frequently used as ornamental tree in urban areas in Turkey and abroad. Cedar scale, Torosaspis cedricola, (Balachowsky & Alkan) (Hemiptera: Diaspididae) is one of the important pests of cedar trees particularly in urban ecosystem. The bio-ecology of T. cedricola on C. libani is examined four localities during the years 2008 and 2009 in Ankara. T. cedricola has two generations in a year and overwinters as mated females. The sex ratio of T. cedricola is changed 1.8:1-4.8:1 (♀:♂) all study areas in both generation and the sex ratio is strongly biased towards female that occur on cedar needles only. The first generation crawlers emerged in late May but the second brood L1 in late July. Adalia bipunctata (L.), Chilocorus bipustulatus (L.), Exochomus quadripustulatus (L.), Harmonia quadripunctata (Pont) (Coleoptera: Coccinellidae) and Cybocephalus fodori minor (Endrödy) (Coleoptera: Cybocephalidae) were determined as predator of the scale, while Diaspiniphagus moeris (Walker) (Hymenoptera: Aphelinidae) was only parasitioid species as natural enemy of T.