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Chromosome-Level Genome Assembly of the Horned-Gall Aphid, Schlechtendalia
bioRxiv preprint doi: https://doi.org/10.1101/2021.02.17.431348; this version posted February 18, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Chromosome-level genome assembly of the horned-gall aphid, Schlechtendalia 2 chinensis (Hemiptera: Aphididae: Erisomatinae) 3 4 Hong-Yuan Wei1#, Yu-Xian Ye2#, Hai-Jian Huang4, Ming-Shun Chen3, Zi-Xiang Yang1*, Xiao-Ming Chen1*, 5 Chuan-Xi Zhang2,4* 6 1Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, China 7 2Institute of Insect Sciences, Zhejiang University, Hangzhou, China 8 3Department of Entomology, Kansas State University, Manhattan, KS, USA 9 4State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products; 10 Key Laboratory of Biotechnology in Plant Protection of MOA of China and Zhejiang Province, Institute of Plant 11 Virology, Ningbo University, Ningbo, China 12 #Contributed equally. 13 *Correspondence 14 Zi-Xiang Yang, Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, China. 15 E-mail: [email protected] 16 Xiao-Ming Chen, Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, China. 17 E-mail: [email protected] 18 Chuan-Xi Zhang, Institute of Insect Sciences, Zhejiang University, Hangzhou, China. 19 E-mail: [email protected] 20 Funding information 21 National Natural Science Foundation of China, Grant/Award number: 31872305, U1402263; The basic research 22 program of Yunnan Province, Grant/Award number: 202001AT070016; The grant for Innovative Team of ‘Insect 23 Molecular Ecology and Evolution’ of Yunnan Province 24 25 Abstract 26 The horned gall aphid Schlechtendalia chinensis, is an economically important insect that induces 27 galls valuable for medicinal and chemical industries. -
More Than Weeds: Non-Crop Plants, Arthropod Predators and Conservation Biological Control
DANY SILVIO SOUZA LEITE AMARAL MORE THAN WEEDS: NON-CROP PLANTS, ARTHROPOD PREDATORS AND CONSERVATION BIOLOGICAL CONTROL Tese apresentada à Universidade Federal de Viçosa, como parte das exigências do Programa de Pós-Graduação em Entomologia, para obtenção do título de Doctor Scientiae. VIÇOSA MINAS GERAIS - BRASIL 2014 DANY SILVIO SOUZA LEITE AMARAL MORE THAN WEEDS: NON-CROP PLANTS, ARTHROPOD PREDATORS AND CONSERVATION BIOLOGICAL CONTROL Tese apresentada à Universidade Federal de Viçosa, como parte das exigências do Programa de Pós-Graduação em Entomologia, para obtenção do título de Doctor Scientiae. APROVADA: 27 de fevereiro 2014. Irene Maria Cardoso Cleide Maria Ferreira Pinto (UFV) (EPAMIG) Angelo Pallini Filho Edison Ryoiti Sujii (Co-orientador) (Co-orientador) (UFV) (EMBRAPA – CENARGEN) Madelaine Venzon (Orientadora) (EPAMIG) De noite há uma flor que corrige os insetos Manoel de Barros – Livro: Anotações de Andarilho. A esperança não vem do mar Nem das antenas de TV A arte de viver da fé Só não se sabe fé em quê Paralamas do Sucesso – Música: Alagados. … a Universidade deve ser flexível, pintar-se de negro, de mulato, de operário, de camponês, ou ficar sem porta, pois o povo a arrombará e ele mesmo a pintará, a Universidade. com as cores que lhe pareça mais adequadas. Ernesto “Che” Guevara – Discurso: Universidade de Las Villas, dezembro de 1959. ii À Fê, que tem sido o amor que inspira minha vida, Ao João, meu filho, meu “Gesù Bambino”, meu “Sítio do Pica-Pau Amarelo”, dedico cada letra, pingo e ponto desta tese. Sem vocês nada aqui faria sentido. iii À tudo aquilo que não sabemos o que é, mas mesmo assim vive, pulsa e movimenta dentro de nós, da natureza e do universo; Aos meus pais, Carlos e Maria Helena, pelo amor, carinho e dedicação irrestritos que sempre tiveram comigo. -
Anatomical Investigations of the Male Reproductive System of Selected Species of Macrosiphini
Bulletin of Insectology 61 (1): 179, 2008 ISSN 1721-8861 Anatomical investigations of the male reproductive system of selected species of Macrosiphini Karina WIECZOREK Department of Zoology, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland Abstract Histological sections and whole mount preparations of five species of Macrosiphini [Impatientinum asiaticum Nevsky, Hypero- myzus (Hyperomyzus) pallidus Hille Ris Lambers, Myzus (Myzus) cerasi (F.), Rhopalomyzus (Judenkoa) loniceare (Siebold) and Uroleucon obscurum (Koch)] were examined. Key words: Hemiptera, Aphidoidea, Aphididae, Macrosiphini, male reproductive system. In previous research on the structure of the male repro- References ductive system of aphids, about 70 species from various subfamilies have been described, mainly Lachninae BLACKMAN R. L., 1987.- Reproduction cytogenetics and de- (Wojciechowski, 1977), Chaitophorinae (Wieczorek and velopment, pp 163-191. In: Aphids, their biology, natural Wojciechowski, 2004), and Calaphidinae (Głowacka et. enemies and control (MINKS A. K., HARREWIJN P., Ed).- El- sevier, Amsterdam, The Netherland. al., 1974; Wieczorek and Wojciechowski, 2001; Wiec- BOCHEN K., KLIMASZEWSKI S. M., WOJCIECHOWSKI W., zorek, 2006). 1975.- Budowa męskiego układu rozrodczego Macrosipho- In contrast, Aphidinae are the largest and most diverse niella artemisiae (B.De Fonsc.) i M. millefolli (De Geer) group of aphids whose male reproductive system is least (Homoptera, Aphididae).- Acta Biologica Uniwersytet Slaski studied. In Pterocommatini the structure of the male re- w Katowicach, 90: 73-81. productive system has been analysed in Pterocomma GŁOWACKA E., KLIMASZEWSKI S. M., SZELEGIEWICZ H., WOJ- populeum (Kaltenbach) (Wieczorek and Wo- CIECHOWSKI W., 1974.- Uber den Bau des mannlichen Fort- jciechowski, 2005) and Pterocomma salicis (L.) (Wiec- pflanzungssystems der Aphiden (Homoptera, Aphidoidea).- zorek and Mróz, 2006), in Aphidini in Rhopalosiphum Annales Universitas Mariae Curie-Skłodowska, 29C: 133-138. -
2021 North American Forest Insect Work Conference
2021 North American Forest Insect Work Conference Shaping Forests: Action in a Changing World May 26-28, 2021 1 2021 North American Forest Insect Work Conference Organizers Organizing Committee: Jess Hartshorn (Chair) – Clemson University, Clemson, SC Brian Aukema – University of Minnesota, St. Paul, MN Rachael Arango – USDA Forest Service, Madison, WI Jeff Garnas – University of New Hampshire, Durham, NH Rich Hofstetter – Northern Arizona University, Flagstaff, AZ Kier Klepzig – The Jones Center at Ichauway, Newton, GA Robert Rabaglia – USDA Forest Service, Washington, DC Program Committee: Kier Klepzig (Co-Chair) – The Jones Center at Ichauway, Newton, GA Rich Hostetter (Co-Chair) – Northern Arizona University, Flagstaff, AZ Deepa Pureswaran – Canadian Forest Service, Quebec, QC Jeff Garnas – University of New Hampshire, Durham, NH Sponsorship: Kevin Chase - Bartlett Tree Experts, Charlotte, NC Posters: Rich Hofstetter - Northern Arizona University 2 Tuesday, May 25 2:00 Forest Health Task Force 4:00 SFIWC Business Meeting WFIWC Business Meeting Wednesday, May 26 8:00 Welcome Remarks 8:15 Plenary Session 1 A. Shannon Lotthammer, Assistant Forestry Commissioner, Minnesota Department of Natural Resources B. EAB impacts: what does the loss of ash mean for wildlife? - Alexis Grinde, Wildlife Ecologist, Natural Resources Research Institute, University of Minnesota - Duluth C. Connections - Eli Sagor, Cloquet Forest, University of Minnesota 9:45 Break 10:30 Student Paper Competition - 1 - Jess Hartshorn A. Following Celtis laevigata Willd. mortality and the commonly associated insects in the southeastern US - Emilee M. Poole, Michael D. Ulyshen, and Scott Horn. Celtis laevigata Willd. (sugarberry) is a native tree commonly found along floodplains and rivers in the southeastern US. -
A Contribution to the Aphid Fauna of Greece
Bulletin of Insectology 60 (1): 31-38, 2007 ISSN 1721-8861 A contribution to the aphid fauna of Greece 1,5 2 1,6 3 John A. TSITSIPIS , Nikos I. KATIS , John T. MARGARITOPOULOS , Dionyssios P. LYKOURESSIS , 4 1,7 1 3 Apostolos D. AVGELIS , Ioanna GARGALIANOU , Kostas D. ZARPAS , Dionyssios Ch. PERDIKIS , 2 Aristides PAPAPANAYOTOU 1Laboratory of Entomology and Agricultural Zoology, Department of Agriculture Crop Production and Rural Environment, University of Thessaly, Nea Ionia, Magnesia, Greece 2Laboratory of Plant Pathology, Department of Agriculture, Aristotle University of Thessaloniki, Greece 3Laboratory of Agricultural Zoology and Entomology, Agricultural University of Athens, Greece 4Plant Virology Laboratory, Plant Protection Institute of Heraklion, National Agricultural Research Foundation (N.AG.RE.F.), Heraklion, Crete, Greece 5Present address: Amfikleia, Fthiotida, Greece 6Present address: Institute of Technology and Management of Agricultural Ecosystems, Center for Research and Technology, Technology Park of Thessaly, Volos, Magnesia, Greece 7Present address: Department of Biology-Biotechnology, University of Thessaly, Larissa, Greece Abstract In the present study a list of the aphid species recorded in Greece is provided. The list includes records before 1992, which have been published in previous papers, as well as data from an almost ten-year survey using Rothamsted suction traps and Moericke traps. The recorded aphidofauna consisted of 301 species. The family Aphididae is represented by 13 subfamilies and 120 genera (300 species), while only one genus (1 species) belongs to Phylloxeridae. The aphid fauna is dominated by the subfamily Aphidi- nae (57.1 and 68.4 % of the total number of genera and species, respectively), especially the tribe Macrosiphini, and to a lesser extent the subfamily Eriosomatinae (12.6 and 8.3 % of the total number of genera and species, respectively). -
Aphids (Hemiptera, Aphididae)
A peer-reviewed open-access journal BioRisk 4(1): 435–474 (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2 435 doi: 10.3897/biorisk.4.57 RESEARCH ARTICLE BioRisk www.pensoftonline.net/biorisk Aphids (Hemiptera, Aphididae) Chapter 9.2 Armelle Cœur d’acier1, Nicolas Pérez Hidalgo2, Olivera Petrović-Obradović3 1 INRA, UMR CBGP (INRA / IRD / Cirad / Montpellier SupAgro), Campus International de Baillarguet, CS 30016, F-34988 Montferrier-sur-Lez, France 2 Universidad de León, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, 24071 – León, Spain 3 University of Belgrade, Faculty of Agriculture, Nemanjina 6, SER-11000, Belgrade, Serbia Corresponding authors: Armelle Cœur d’acier ([email protected]), Nicolas Pérez Hidalgo (nperh@unile- on.es), Olivera Petrović-Obradović ([email protected]) Academic editor: David Roy | Received 1 March 2010 | Accepted 24 May 2010 | Published 6 July 2010 Citation: Cœur d’acier A (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2. In: Roques A et al. (Eds) Alien terrestrial arthropods of Europe. BioRisk 4(1): 435–474. doi: 10.3897/biorisk.4.57 Abstract Our study aimed at providing a comprehensive list of Aphididae alien to Europe. A total of 98 species originating from other continents have established so far in Europe, to which we add 4 cosmopolitan spe- cies of uncertain origin (cryptogenic). Th e 102 alien species of Aphididae established in Europe belong to 12 diff erent subfamilies, fi ve of them contributing by more than 5 species to the alien fauna. Most alien aphids originate from temperate regions of the world. Th ere was no signifi cant variation in the geographic origin of the alien aphids over time. -
Artemisia Vulgaris (Mugwort)
Artemisia vulgaris Artemisia vulgaris Mugwort Introduction The genus Artemisia includes more than 300 species, which are distributed Photo unavailable primarily in temperate regions and subtropics of Asia, Europe and North America. In China, there are 186 species and 44 varieties belonging to 2 subgenera with a nationwide distribution. Members of the genus Artemisia are well-known as aromatic herbs[103]. Species of Artemisia in China (see next page) long densely ciliate hairs at the top of Leaves of Artemisia vulgaris. Taxonomy the style. Fruits, appearing from August Family: Compositae to October together with flowers, are [103] Economic Importance (Asteraceae) obovate or ovate achenes . In addition to the volatile oil psilostachyin, Genus: Artemisia L. which contributes to its strong aroma, Habitat mugwort also contains other medically Description Mugwort grows in high-elevation pastures, active ketones and alkaloids. Mugwort Commonly known as mugwort, Artemisia forest edges, valleys, hillside wasteland, is also used as a livestock feed[103]. [112][103] vulgaris is a perennial herb that can ditches, and roadsides . reach 60-160 cm high, with many thin Related Species lateral roots. The branched, purplish- Distribution In China, mugwort, the common name brown stems are parallel grooved, with In China, mugwort has been reported of Artemisia vulgaris is often confused ascending twigs covered with short to occur in Shaanxi and Qinghai at with A. argyi, which is a common hairs. Leaves are papery, pubescent, elevations above 2,500 m, as well inhabitant of wastelands, roadsides, dark green on the upper surface, and as in western Gansu and Xinjiang at riversides, and hilly slopes, as well [103] have various shapes depending on elevations of 1,500 to 2,100 m . -
White Plant Shoots, Wax-Producing Insects and Other White Structures Made by Arthropods: a Mimicry Complex?
EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 114: 343–349, 2017 http://www.eje.cz doi: 10.14411/eje.2017.043 POINT OF VIEW White plant shoots, wax-producing insects and other white structures made by arthropods: A mimicry complex? KAZUO YAMAZAKI Osaka Institute of Public Health, 8-34 Tojo-cho, Tennoji, Osaka 543-0026, Japan; e-mail: [email protected]. jp Key words. Plant mimicry, anti-herbivore defence, cocoon, entomopathogenic fungus, spider egg sac, spittlebug froth, trichome, wax Abstract. Many insects masquerade as parts of plants, such as bark or leaves, or mimic poisonous organisms in order to defend themselves against predators. However, recent studies indicate that plants may mimic insects and other arthropods to deter herbi- vores. Here, I report visually similar white structures of plants and arthropods in Japan and suggest they are part of a mimicry com- plex. Young shoots covered with white trichomes or waxy substances may mimic wax-producing insects, such as woolly aphids, coccids and caterpillars, potentially resulting in reduced herbivory. Since wax-producing insects would reduce plant quality and quantity, be distasteful and attract natural enemies, herbivorous insects and mammals may avoid such white shoots. Furthermore, fungus-infected insects, gregarious braconid cocoons, spider egg sacs and froth made by froghopper nymphs or blasticotomid sawfl y larvae are also conspicuously white and impose risks for herbivorous insects. Thus, these white structures may be mimicry models for white shoots and are likely to be part of a defensive mimicry complex. Although this study focuses on defence against herbivores, there are simultaneous physiological roles for white colouration that will not be discussed in depth here. -
Phylogenetic Implications of the Structure of the Alimentary Tract of the Aphidoidea
WAGENINGEN AGRICULTURAL UNIVERSITY PAPERS 90-4(1990) Phylogeneticimplication s ofth e structure ofth ealimentar y tract ofth e Aphidoidea I. Greenidea, Israelaphisan d Neopyllaphis II.Th eAphis-gxouQ M.B .Ponse n Laboratory of Virology, Agricultural University Wageningen, The Netherlands Wageningen MM Agricultural University \yn S2.\ ^ •'•> Cip-data Koninklijke Bibliotheek, Den Haag Ponsen, M.B. Phylogenetic implications ofth estructur e ofth ealimentar y tract ofth e Aphidoi- dea / M.B. Ponsen. Wageningen: Agricultural University. - 111. -(Wageninge n Agricultural Univer sitypapers , ISSN 0169-345X; 90-4(1990) Contains: I. Greenidea, Israelaphis and Neopyllaphis; II. The Aphis-group. - With ref. ISBN 90-6754-169-9 SISO 597.89 UDC 595.75:591.132 NUGI835 Subject headings: aphids / histology / Lightmicroscopy. ISBN 90-6754-169-9 NUGI 835 © Agricultural University Wageningen, The Netherlands, 1990 No part of this publication, apart from abstract, bibliographic and brief quo tations embodied incritica l reviews,ma y bereproduced , re-corded or published inan y form including print, photocopy, microform, elektronic or elektromagne- ticrecor d without written permission from the publisher Agricultural Universi ty, P.O.Box 9101, 6700H B Wageningen, the Netherlands. Printed in the Netherlands by Drukkerij Veenman B.V., Wageningen BIBLIOTHEEK LAJSDBOIJWUNIVERSITEIl SPAGENINGEN Contents Part I. Greenidea,Israelaphis and Neophyllaphis Introduction 3 Materials and methods 3 Results 4 Discussion 12 Summary 17 Acknowledgements 17 References 18 Abbreviations used in figures 19 Part II. The Aphis-group 21 Introduction 23 Materials and methods 23 Results 25 Discussion 43 Summary 48 Acknowledgements 49 References 49 Abbreviations used in figures 51 ym\ mo CB-KARDEX Part I. Greenidea, Israelaphis, and Neophyllaphis Introduction In Börner'sclassificatio n of aphids thegenu s Greenideai sassigne d to the family Chaitophoridae, and the genus Neophyllaphis to the family Thelaxidae (Borner and Heinze, 1957). -
Hemiptera: Aphididae) in Hawaii
FPirstroceedin recordGs of For the G reenidiahawaiian fiscicola entomolo Gical society (2012) 44:83–84 83 New Records and Accounts First Records for the Aphid Greenidea ficicola Takahashi (Hemiptera: Aphididae) in Hawaii Walter T. Nagamine and Janis N. Garcia Hawaii Department of Agriculture, Plant Pest Control Branch, 1428 S. King St., Honolulu, HI 96822; [email protected], [email protected] Abstract. First observations of the aphid Greenidea ficicola are recorded from Hawaii, which was found infesting Chinese banyan, Ficus microcarpa, at Kahaluu, Oahu, on January 6, 2011. This is the second species of the Asian genus Greenidea to become established in Hawaii. Key words: Greenidea ficicola, new state record, Hawaii A new aphid to the state of Hawaii, ficicolain the United States was in Florida Greenidea ficicola Takahashi, was collect- in 2002. Host plants are restricted to Ficus ed on Chinese banyan (Ficus microcarpa) spp. throughout most of its range, although at Kahaluu, Oahu on January 6th and 11th, in India it has been collected from guava, 2011. At this time, aphids infesting F. Psidium guajava (Halbert 2004). microcarpa were uncommon in Hawaii, In Hawaii, a related species, G. psidii prompting a closer examination of these van Der Goot (= G. formosana Maki), was specimens. Slide-mounted adult aphids first recorded in 1993 infesting leaves of a were submitted to the Systematic Ento- guava tree at the University of Hawaii at mology Laboratory, Agricultural Research Manoa campus (Beardsley 1995). While Service, U.S. Department of Agriculture, its geographic distribution is nearly and identified on July 6, 2011 asGreenidea similar to that of G. -
Phylogenetics and Evolution of the Aphid Genus Uroleucon Based on Mitochondrial and Nuclear DNA Sequences
R Systematic Entomology (1999) 24, 85±93 Phylogenetics and evolution of the aphid genus Uroleucon based on mitochondrial and nuclear DNA sequences NANCY A. MORAN, MATTHEW E. KAPLAN, MICHAEL J. GELSEY, TROY G. MURPHY and EDWIN A. SCHOLES Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, U.S.A. Abstract. The genus Uroleucon, and the related genus Macrosiphoniella, represent a large Tertiary radiation of aphids, with a total of about 300 species distributed throughout the world, primarily on host plant species in the family Asteraceae. A molecular phylogenetic study was conducted to identify major clades within Uroleucon and to address the cladistic validity of current subgeneric categories, the evolution of host plant associations, the age of origin, and intercontinental movements in this genus. The seventeen study species included members of the three major subgenera of Uroleucon, species from Europe and North America, one member of Macrosiphoniella, and two outgroups. Data consisted of DNA sequences for three mitochondrial regions and the nuclear gene EF1alpha, for a total of 4287 sites. Nodes supported strongly in both parsimony and maximum likelihood analyses suggest that: (1) Nearctic Uromelan are a monophyletic group branching near the base of the genus and not related to European Uromelan, (2) the New World subgenus Lambersius is possibly monophyletic but is not a tightly related group and is not closely related to other North American species, and (3) Nearctic members of subgenus Uroleucon are a closely related monophyletic group not allied with Nearctic Uromelan or Lambersius. Instead they represent a separate colonization by an Old World ancestor, as they are nested within a strongly supported clade containing European members of both subgenera Uroleucon and Uromelan. -
Aphid Transmission of Potyvirus: the Largest Plant-Infecting RNA Virus Genus
Supplementary Aphid Transmission of Potyvirus: The Largest Plant-Infecting RNA Virus Genus Kiran R. Gadhave 1,2,*,†, Saurabh Gautam 3,†, David A. Rasmussen 2 and Rajagopalbabu Srinivasan 3 1 Department of Plant Pathology and Microbiology, University of California, Riverside, CA 92521, USA 2 Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC 27606, USA; [email protected] 3 Department of Entomology, University of Georgia, 1109 Experiment Street, Griffin, GA 30223, USA; [email protected] * Correspondence: [email protected]. † Authors contributed equally. Received: 13 May 2020; Accepted: 15 July 2020; Published: date Abstract: Potyviruses are the largest group of plant infecting RNA viruses that cause significant losses in a wide range of crops across the globe. The majority of viruses in the genus Potyvirus are transmitted by aphids in a non-persistent, non-circulative manner and have been extensively studied vis-à-vis their structure, taxonomy, evolution, diagnosis, transmission and molecular interactions with hosts. This comprehensive review exclusively discusses potyviruses and their transmission by aphid vectors, specifically in the light of several virus, aphid and plant factors, and how their interplay influences potyviral binding in aphids, aphid behavior and fitness, host plant biochemistry, virus epidemics, and transmission bottlenecks. We present the heatmap of the global distribution of potyvirus species, variation in the potyviral coat protein gene, and top aphid vectors of potyviruses. Lastly, we examine how the fundamental understanding of these multi-partite interactions through multi-omics approaches is already contributing to, and can have future implications for, devising effective and sustainable management strategies against aphid- transmitted potyviruses to global agriculture.