Eriophyoidea and Allies: Where Do They Belong?
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NDP 39 Hazelnut Big Bud Mite
NDP ## V# - National Diagnostic Protocol for Phytoptus avellanae National Diagnostic Protocol Phytoptus avellanae Nalepa Hazelnut big bud mite NDP 39 V1 NDP 39 V1 - National Diagnostic Protocol for Phytoptus avellanae © Commonwealth of Australia Ownership of intellectual property rights Unless otherwise noted, copyright (and any other intellectual property rights, if any) in this publication is owned by the Commonwealth of Australia (referred to as the Commonwealth). Creative Commons licence All material in this publication is licensed under a Creative Commons Attribution 3.0 Australia Licence, save for content supplied by third parties, logos and the Commonwealth Coat of Arms. Creative Commons Attribution 3.0 Australia Licence is a standard form licence agreement that allows you to copy, distribute, transmit and adapt this publication provided you attribute the work. A summary of the licence terms is available from http://creativecommons.org/licenses/by/3.0/au/deed.en. The full licence terms are available from https://creativecommons.org/licenses/by/3.0/au/legalcode. This publication (and any material sourced from it) should be attributed as: Subcommittee on Plant Health Diagnostics (2017). National Diagnostic Protocol for Phytoptus avellanae – NDP39 V1. (Eds. Subcommittee on Plant Health Diagnostics) Author Davies, J; Reviewer Knihinicki, D. ISBN 978-0-9945113-9-3 CC BY 3.0. Cataloguing data Subcommittee on Plant Health Diagnostics (2017). National Diagnostic Protocol for Phytoptus avellanae NDP39 V1. (Eds. Subcommittee on Plant Health -
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Biologia 67/3: 546—560, 2012 Section Zoology DOI: 10.2478/s11756-012-0025-x Measuring the host specificity of plant-feeding mites based on field data – a case study of the Aceria species Anna Skoracka1 &Lechoslaw Kuczynski´ 2 1Department of Animal Taxonomy and Ecology, Institute of Environmental Biology, Faculty of Biology, Adam Mickiewicz University, Umultowska 89, 61–614 Pozna´n, Poland; e-mail: [email protected] 2Department of Avian Biology, Institute of Environmental Biology, Faculty of Biology, Adam Mickiewicz University, Umul- towska 89, 61–614 Pozna´n, Poland; e-mail: [email protected] Abstract: For the majority of eriophyoid species, host ranges have been established purely on the basis of collection records, usually without quantitative data. The aim of this study was to: (1) quantitatively examine published literature to explore whether relevant analyses of field-collected quantitative data were used to assess host specificity of herbivores; (2) propose a protocol for data analysis that could be applied to plant-feeding mites; (3) analyse host specificity of the grass-feeding Aceria species as a case study. Field data were collected in Central and Northern Europe over a period of 11 years, and included 73 grass species. For the eight Aceria species found, infestation parameters and host specificity indexes were assessed. Accumulation curves were calculated to study how the sampling effort influenced estimates of host specificity indexes. A literature analysis showed that among the studies that declared an aim of estimating the host range only 56% of them applied any quantitative analysis or informed on estimation reliability. The analysis of field-collected data and its interpretation showed the most complete and reliable conclusions about the host specificity of Aceria species when all indices were considered and, if available, other information about the mite’s ecology and biology. -
Diverse Mite Family Acaridae
Disentangling Species Boundaries and the Evolution of Habitat Specialization for the Ecologically Diverse Mite Family Acaridae by Pamela Murillo-Rojas A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy (Ecology and Evolutionary Biology) in the University of Michigan 2019 Doctoral Committee: Associate Professor Thomas F. Duda Jr, Chair Assistant Professor Alison R. Davis-Rabosky Associate Professor Johannes Foufopoulos Professor Emeritus Barry M. OConnor Pamela Murillo-Rojas [email protected] ORCID iD: 0000-0002-7823-7302 © Pamela Murillo-Rojas 2019 Dedication To my husband Juan M. for his support since day one, for leaving all his life behind to join me in this journey and because you always believed in me ii Acknowledgements Firstly, I would like to say thanks to the University of Michigan, the Rackham Graduate School and mostly to the Department of Ecology and Evolutionary Biology for all their support during all these years. To all the funding sources of the University of Michigan that made possible to complete this dissertation and let me take part of different scientific congresses through Block Grants, Rackham Graduate Student Research Grants, Rackham International Research Award (RIRA), Rackham One Term Fellowship and the Hinsdale-Walker scholarship. I also want to thank Fulbright- LASPAU fellowship, the University of Costa Rica (OAICE-08-CAB-147-2013), and Consejo Nacional para Investigaciones Científicas y Tecnológicas (CONICIT-Costa Rica, FI- 0161-13) for all the financial support. I would like to thank, all specialists that help me with the identification of some hosts for the mites: Brett Ratcliffe at the University of Nebraska State Museum, Lincoln, NE, identified the dynastine scarabs. -
An Ultrastructural Study of the Relationship Between the Mite Floracarus Perrepae Knihinicki & Boczek (Acariformes:Eriophyidae) and the Fern
1 Running title: Floracarus ultrastructure For submission to Australian Journal of Entomology An ultrastructural study of the relationship between the mite Floracarus perrepae Knihinicki & Boczek (Acariformes:Eriophyidae) and the fern Lygodium microphyllum (Cav.) R. Br. (Lygodiaceae) Thomas P. Freeman,1* John A. Goolsby,2 Sebahat K. Ozman,3 Dennis R. Nelson4 1North Dakota State University, Department of Plant Pathology, Northern Crop Science Laboratory, Fargo, North Dakota, USA 2USDA-ARS, Australian Biological Control Laboratory, 120 Meiers Road, Indooroopilly, 4068, Brisbane, Queensland, Australia 3CRC for Tropical Plant Protection and Dept. of Zoology and Entomology, The University of Queensland, 4072, Brisbane, QLD, Australia; current address, Ondokuz Mayis University, Faculty of Agriculture, Department of Plant Protection, 55139, Samsun, Turkey 4USDA-ARS, Biosciences Research Laboratory, 1605 Albrecht Blvd, Fargo, North Dakota, USA *Corresponding author (email: [email protected], telephone: 701-231-8234, facsimile: 701-239-1395) 2 ABSTRACT The ultrastructure of Floracarus perrepae was investigated in relation to its host, Lygodium microphyllum. Feeding by the mite induces a change in epidermal cell size, and cell division is stimulated by mite feeding, causing the leaf margin to curl over into a roll with two to three windings. The enlarged epidermal layer greatly increases its cytoplasmic contents, which become a nutritive tissue for the mite and its progeny. The structure and depth of stylet penetration by the mite, and the thickness of the epidermal cell wall of L. microphyllum, does not appear to account for the mite’s differential ability to induce leaf rolling in its co- adapted host from southeast Queensland but not in the invasive genotype of the fern in Florida. -
Number 73 April, 2018
ARAB AND NEAR EAST PLANT PROTECTION NEWSLETTER Number 73 April, 2018 Editor-in-Chief Ibrahim Al-JBOORY – Faculty of Agriculture, Baghdad University, Iraq. Editorial Board Bassam BAYAA – Faculty of Agriculture, University of Aleppo, Aleppo, Syria. Khaled MAKKOUK – National Council for Scientific Research, Beirut, Lebanon. Shoki AL-DOBAI – International Plant Protection Convention Secretariat, FAO, Rome Ahmed DAWABAH – Plant Pathology Research Institute, Agricultural Research Center, Egypt Ahmed EL-HENEIDY – Plant Protection Research Institute, ARC, Giza, Egypt. Safaa KUMARI – International Centre for Agricultural Research in the Dry Areas (ICARDA), Tunis, Tunisia. Mustafa HAIDAR – Faculty of Agricultural and Food Sciences, AUB, Lebanon. Ahmed KATBEH – Faculty of Agriculture, University of Jordan, Amman, Jordan. Bouzid NASRAOUI – INAT, University of Carthage, Tunis, Tunisia. Wa’el ALMATNI – Ministry of Agriculture, Damascus, Syria. Editorial Assistant Tara ALFADHLI – P.O. Box 17399, Amman11195, Jordan. The Arab Society for Plant Protection and the Near East Regional Office of the FAO jointly publishes the Arab and Near East Plant Protection Newsletter (ANEPPNEL), three times per year. All correspondence should be sent by email to the Editor ([email protected]). Material from ANEPPNEL may be reprinted provided that appropriate credits are given. The designations employed and the presentation of material in this newsletter do not necessarily imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization (FAO) of the United Nations or the Arab Society for Plant Protection (ASPP), concerning the legal or constitutional status of any country, territory, city or area, or its authorities or concerning the delimitation of its frontiers or boundaries. Similarly, views expressed by any contributor to the newsletter are those of the contributor only, and must not be regarded as conforming to the views of FAO or ASPP. -
Catálogo De Ácaros Eriofioideos (Acari: Trombidiformes) Parasitados Por Especies De Hirsutella (Deuteromycetes) En Cuba
ARTÍCULO: Catálogo de ácaros eriofioideos (Acari: Trombidiformes) parasitados por especies de Hirsutella (Deuteromycetes) en Cuba Reinaldo I. Cabrera, Pedro de la Torre & Gabriel Otero-Colina Resumen: Se revisó la base de datos de la colección de especies del género Hirsutella y otros hongos acaropatógenos y entomopatógenos presente en el IIFT (Institu- ARTÍCULO: to de Investigaciones en Fruticultura Tropical) de Ciudad de La Habana, Cuba, Catálogo de ácaros eriofioideos así como la información bibliográfica adicional sobre el tema. Se relacionan (Acari: Trombidiformes) parasitados por primera vez 16 eriofioideos como nuevos registros de hospedantes de por especies de Hirsutella (Deute- especies de Hirsutella, los que junto a otros nueve ya conocidos en el país, romycetes) en Cuba suman 25. Se señalan 16 especies vegetales como nuevos registros de hospedantes de ácaros eriofioideos parasitados por estos hongos, las que se Reinaldo I. Cabrera suman a nueve ya existentes. Se ofrecen datos sobre la distribución geográfi- Instituto de Investigaciones en ca e importancia del parasitismo de los ácaros eriofioideos por especies de Hir- Fruticultura Tropical. sutella. Ave. 7ma # 3005 e/ 30 y 32 Palabras clave: Diptilomiopidae, Eriophyidae, Phytoptidae, parasitismo, plantas Playa C. de La Habana hospedantes. C.P. 11300, Zona Postal 13, Cuba. [email protected] Pedro de la Torre Laboratorio Central de Cuarentena Catalogue of eriophyoideus mites (Acari: Trombidiformes) parasited Vegetal. Ayuntamiento Nº 231 by Hirsutella species (Deuteromycetes) in Cuba Plaza, Ciudad de La Habana. Cuba. [email protected] Abstract: Gabriel Otero-Colina The database of the collection of Hirsutella species and other acaropathogenic Colegio de Postgraduados, Campus and entomopathogenic fungi from the IIFT (Research Institute on Tropical Fruit Montecillo. -
Genome and Metagenome of the Phytophagous Gall-Inducing Mite Fragariocoptes Setiger (Eriophyoidea): Are Symbiotic Bacteria Responsible for Gall-Formation?
Genome and Metagenome of The Phytophagous Gall-Inducing Mite Fragariocoptes Setiger (Eriophyoidea): Are Symbiotic Bacteria Responsible For Gall-Formation? Pavel B. Klimov ( [email protected] ) X-BIO Institute, Tyumen State University Philipp E. Chetverikov Saint-Petersburg State University Irina E. Dodueva Saint-Petersburg State University Andrey E. Vishnyakov Saint-Petersburg State University Samuel J. Bolton Florida Department of Agriculture and Consumer Services, Gainesville, Florida, USA Svetlana S. Paponova Saint-Petersburg State University Ljudmila A. Lutova Saint-Petersburg State University Andrey V. Tolstikov X-BIO Institute, Tyumen State University Research Article Keywords: Agrobacterium tumefaciens, Betabaculovirus Posted Date: August 20th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-821190/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/16 Abstract Eriophyoid mites represent a hyperdiverse, phytophagous lineage with an unclear phylogenetic position. These mites have succeeded in colonizing nearly every seed plant species, and this evolutionary success was in part due to the mites' ability to induce galls in plants. A gall is a unique niche that provides the inducer of this modication with vital resources. The exact mechanism of gall formation is still not understood, even as to whether it is endogenic (mites directly cause galls) or exogenic (symbiotic microorganisms are involved). Here we (i) investigate the phylogenetic anities of eriophyoids and (ii) use comparative metagenomics to test the hypothesis that the endosymbionts of eriophyoid mites are involved in gall-formation. Our phylogenomic analysis robustly inferred eriophyoids as closely related to Nematalycidae, a group of deep-soil mites belonging to Endeostigmata. -
Genetic and Morphological Diversity of Trisetacus Species
Exp Appl Acarol (2014) 63:497–520 DOI 10.1007/s10493-014-9805-z Genetic and morphological diversity of Trisetacus species (Eriophyoidea: Phytoptidae) associated with coniferous trees in Poland: phylogeny, barcoding, host and habitat specialization Mariusz Lewandowski • Anna Skoracka • Wiktoria Szydło • Marcin Kozak • Tobiasz Druciarek • Don A. Griffiths Received: 31 October 2013 / Accepted: 15 March 2014 / Published online: 8 April 2014 Ó The Author(s) 2014. This article is published with open access at Springerlink.com Abstract Eriophyoid species belonging to the genus Trisetacus are economically important as pests of conifers. A narrow host specialization to conifers and some unique morphological characteristics have made these mites interesting subjects for scientific inquiry. In this study, we assessed morphological and genetic variation of seven Trisetacus species originating from six coniferous hosts in Poland by morphometric analysis and molecular sequencing of the mitochondrial cytochrome oxidase subunit I gene and the nuclear D2 region of 28S rDNA. The results confirmed the monophyly of the genus Tris- etacus as well as the monophyly of five of the seven species studied. Both DNA sequences were effective in discriminating between six of the seven species tested. Host-dependent genetic and morphological variation in T. silvestris and T. relocatus, and habitat-dependent M. Lewandowski (&) Á T. Druciarek Department of Applied Entomology, Faculty of Horticulture, Biotechnology and Landscape Architecture, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159, 02-776 Warsaw, Poland e-mail: [email protected] T. Druciarek e-mail: [email protected] A. Skoracka Á W. Szydło Department of Animal Taxonomy and Ecology, Faculty of Biology, Adam Mickiewicz University, Umultowska 89, 61-614 Poznan, Poland e-mail: [email protected] W. -
Supplementary Description of Novophytoptus Stipae Keifer 1962
Systematic & Applied Acarology 22(2): 253–270 (2017) ISSN 1362-1971 (print) http://doi.org/10.11158/saa.22.2.9 ISSN 2056-6069 (online) Article http://zoobank.org/urn:lsid:zoobank.org:pub:5A8972C2-4983-4CC1-BA46-CAC0DCCB2AD2 Supplementary description of Novophytoptus stipae Keifer 1962 (Acariformes, Eriophyoidea) with LT-SEM observation on mites from putatively conspecific populations: cryptic speciation or polyphagy of novophytoptines on phylogenetically remote hosts? PHILIPP E. CHETVERIKOV1,2,3,6, JAMES AMRINE4, GARY BAUCHAN5, RON OCHOA5, SOGDIANA I. SUKHAREVA2 & ANDREY E. VISHNYAKOV2 1 Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, 199034 St. Petersburg, Russia 2 Saint-Petersburg State University, Universitetskaya nab., 7/9, 199034, St. Petersburg, Russia 3 Tyumen State University, Semakova Str., 10, 625003, Tyumen, Russia 4 West Virginia University, Division of Plant & Soil Sciences, P.O.Box 6108, Morgantown, WV 26506-6108, USA 5 USDA-ARS, Electron & Confocal Microscopy Unit, Beltsville, Maryland, 20705, USA 6 Corresponding author: [email protected] Abstract Supplementary descriptions of an infrequently encountered species Novophytoptus stipae Keifer 1962 (Eriophyoidea, Phytoptidae) from Achnatherum speciosum (Poaceae) based on topotypes recovered from dry plant material from California is given. Comparison of topotypes of N. stipae with fresh Novophytoptus mites from Juncus tenuis and J. balticus (Juncaceae) collected in West Virginia and Ohio failed to reveal distinct morphological differences sufficient enough to establish new taxa. All studied mites are considered belonging to one species, N. stipae. This is putatively an example of polyphagous eriophyoid species inhabiting phylogenetically remote hosts. Remarks on polyphagy and dispersal modes in eriophyoids are addressed. Uncommon features of the gnathosoma and the anal region of novophytoptines were discovered under LT-SEM. -
An Ultrastructural Study of the Relationship Between The
et al . Australian Journal of Entomology (2005) 44, 57–61 An ultrastructural study of the relationship between the mite Floracarus perrepae Knihinicki & Boczek (Acariformes: Eriophyidae) and the fern Lygodium microphyllum (Lygodiaceae) Thomas P Freeman,1* John A Goolsby,2 Sebahat K Ozman3† and Dennis R Nelson4 1North Dakota State University, Department of Plant Pathology, Northern Crop Science Laboratory, Fargo, ND 58105- 5517, USA. 2USDA-ARS, Australian Biological Control Laboratory, 120 Meiers Road, Indooroopilly, Qld 4068, Australia. 3CRC for Tropical Plant Protection and Department of Zoology and Entomology, The University of Queensland, Qld 4072, Australia. 4USDA-ARS, Biosciences Research Laboratory, 1605 Albrecht Blvd, Fargo, ND 58105, USA. Abstract The ultrastructure of the mite Floracarus perrepae was investigated in relation to its host, Lygodium microphyllum, the Old World climbing fern. Floracarus perrepae has been suggested as a means of biological control for the fern, which is an aggressive weed in tropical areas. Feeding by the mite induces a change in the size of epidermal cells, and cell division is stimulated by mite feeding, causing the leaf margin to curl over into a roll with two to three windings. The enlarged epidermal layer greatly increases its cytoplasmic contents, which become a nutritive tissue for the mite and its progeny. Damage by the mite ultimately debilitates the fern. The structure and depth of stylet penetration by the mite, and the thickness of the epidermal cell wall of L. microphyllum, do not appear to account for the mite’s differential ability to induce leaf rolling in its co-adapted host from south-east Queensland but not in the invasive genotype of the fern in Florida. -
Fine Structure of Receptor Organs in Oribatid Mites (Acari)
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Biosystematics and Ecology Jahr/Year: 1998 Band/Volume: 14 Autor(en)/Author(s): Alberti Gerd Artikel/Article: Fine structure of receptor organs in oribatid mites (Acari). In: EBERMANN E. (ed.), Arthropod Biology: Contributions to Morphology, Ecology and Systematics. 27-77 Ebermann, E. (Ed) 1998:©Akademie Arthropod d. Wissenschaften Biology: Wien; Contributions download unter towww.biologiezentrum.at Morphology, Ecology and Systematics. - Biosystematics and Ecology Series 14: 27-77. Fine structure of receptor organs in oribatid mites (Acari) G. A l b e r t i Abstract: Receptor organs of oribatid mites represent important characters in taxonomy. However, knowledge about their detailed morphology and function in the living animal is only scarce. A putative sensory role of several integumental structures has been discussed over years but was only recently clarified. In the following the present state of knowledge on sensory structures of oribatid mites is reviewed. Setiform sensilla are the most obvious sensory structures in Oribatida. According to a clas- sification developed mainly by Grandjean the following types are known: simple setae, trichobothria, eupathidia, famuli and solenidia. InEupelops sp. the simple notogastral setae are innervated by two dendrites terminating with tubulär bodies indicative of mechanore- ceptive cells. A similar innervation was seen in trichobothria ofAcrogalumna longipluma. The trichobothria are provided with a setal basis of a very high complexity not known from other arthropods. The setal shafts of these two types of sensilla are solid and without pores. They thus represent so called no pore sensilla (np-sensilla). -
Present Status of Eriophyoid Mites in Thailand
J. Acarol. Soc. Jpn., 25(S1): 83-107. March 25, 2016 © The Acarological Society of Japan http://www.acarology-japan.org/ 83 Present status of eriophyoid mites in Thailand 1 2 3 Angsumarn CHANDRAPATYA *, Ploychompoo KONVIPASRUANG and James W. AMRINE 1Department of Entomology, Faculty of Agriculture, Kasetsart University, 50 Ngam Wong Wan Road, Chatuchak, Bangkok 10900, Thailand 2Plant Protection Research and Development Office, Department of Agriculture, Paholyothin Road, Chatuchak, Bangkok 10900, Thailand 3Division of Plant and Soil Sciences, College of Agriculture and Forestry, West Virginia University, P. O. Box 6108, Morgantown, WV 26506-6108, USA ABSTRACT One of the common groups of phytophagous mites encountered on various plants in Thailand is that of the eriophyoid mites, which can be found on agricultural, horticultural, ornamental, and medicinal plants, including fruit and forest trees. Because there is a paucity of information on eriophyoid taxonomy in Thailand, where the host plants are so diverse, there is a need to investigate the presence of these tiny creatures – especially those species that can be harmful to economic crops. Here, the taxonomy of the eriophyoid mites in the collection of the first author was revised, together with the taxonomy of those reported by other researchers. To date, a total of 215 species of eriophyoid mites have been recorded from Thailand. The family Eriophyidae comprises 157 species, whereas only 58 species are reported in the family Diptilomiopidae. These mites are found on 161 plant species under 60 host plant families; they are relatively more numerous (>10 species) on plants in the families Fabaceae, Poaceae, Moraceae, Sapindaceae, Rubiaceae, Anacardiaceae, Myrtaceae, and Euphorbiaceae.