Gall-Making Insects and Mites Michael Merchant*
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Leafy and Crown Gall
Is it Crown Gall or Leafy Gall? Melodie L. Putnam and Marilyn Miller Humphrey Gifford, an early English poet said, “I cannot say the crow is white, But needs must call a spade a spade.” To call a thing by its simplest and best understood name is what is meant by calling a spade a spade. We have found confusion around the plant disease typified by leafy galls and shoot proliferation, and we want to call a spade a spade. The bacterium Rhodococcus fascians causes fasciation, leafy galls and shoot proliferation on plants. These symptoms have been attributed variously to crown gall bacteria (Agrobacterium tumefaciens), virus infection, herbicide damage, or eriophyid mite infestation. There is also confusion about what to call the Figure 1. Fasciation (flattened growth) of a pumpkin symptoms caused by R. fascians. Shoot stem, which may be due to disease, a genetic proliferation and leafy galls are sometimes condition, or injury. called “fasciation,” a term also used to refer to tissues that grow into a flattened ribbon- like manner (Figure 1). The root for the word fasciation come from the Latin, fascia, to fuse, and refers to a joining of tissues. We will reserve the term fasciation for the ribbon like growth of stems and other organs. The terms “leafy gall” and “shoot proliferation” are unfamiliar to many people, but are a good description of what is seen on affected plants. A leafy gall is a mass of buds or short shoots tightly packed together and fused at the base. These may appear beneath the soil or near the soil line at the base of the stem (Figure 2). -
The Structure of Cynipid Oak Galls: Patterns in the Evolution of an Extended Phenotype
The structure of cynipid oak galls: patterns in the evolution of an extended phenotype Graham N. Stone1* and James M. Cook2 1Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK ([email protected]) 2Department of Biology, Imperial College, Silwood Park, Ascot, Berkshire SL5 7PY, UK Galls are highly specialized plant tissues whose development is induced by another organism. The most complex and diverse galls are those induced on oak trees by gallwasps (Hymenoptera: Cynipidae: Cyni- pini), each species inducing a characteristic gall structure. Debate continues over the possible adaptive signi¢cance of gall structural traits; some protect the gall inducer from attack by natural enemies, although the adaptive signi¢cance of others remains undemonstrated. Several gall traits are shared by groups of oak gallwasp species. It remains unknown whether shared traits represent (i) limited divergence from a shared ancestral gall form, or (ii) multiple cases of independent evolution. Here we map gall character states onto a molecular phylogeny of the oak cynipid genus Andricus, and demonstrate three features of the evolution of gall structure: (i) closely related species generally induce galls of similar structure; (ii) despite this general pattern, closely related species can induce markedly di¡erent galls; and (iii) several gall traits (the presence of many larval chambers in a single gall structure, surface resins, surface spines and internal air spaces) of demonstrated or suggested adaptive value to the gallwasp have evolved repeatedly. We discuss these results in the light of existing hypotheses on the adaptive signi¢cance of gall structure. Keywords: galls; Cynipidae; enemy-free space; extended phenotype; Andricus layers of woody or spongy tissue, complex air spaces within 1. -
National Oak Gall Wasp Survey
ational Oak Gall Wasp Survey – mapping with parabiologists in Finland Bess Hardwick Table of Contents 1. Introduction ................................................................................................................. 2 1.1. Parabiologists in data collecting ............................................................................. 2 1.2. Oak cynipid gall wasps .......................................................................................... 3 1.3. Motivations and objectives .................................................................................... 4 2. Material and methods ................................................................................................ 5 2.1. The volunteers ........................................................................................................ 5 2.2. Sampling ................................................................................................................. 6 2.3. Processing of samples ............................................................................................ 7 2.4. Data selection ........................................................................................................ 7 2.5. Statistical analyses ................................................................................................. 9 3. Results ....................................................................................................................... 10 3.1. Sampling success ................................................................................................. -
Butlleti 71.P65
Butll. Inst. Cat. Hist. Nat., 71: 83-95. 2003 ISSN: 1133-6889 GEA, FLORA ET FAUNA The life cycle of Andricus hispanicus (Hartig, 1856) n. stat., a sibling species of A. kollari (Hartig, 1843) (Hymenoptera: Cynipidae) Juli Pujade-Villar*, Roger Folliot** & David Bellido* Rebut: 28.07.03 Acceptat: 01.12.03 Abstract and so we consider A. mayeti and A. niger to be junior synonyms of A. hispanicus. Finally, possible causes of the speciation of A. kollari and The marble gallwasp, Andricus kollari, common A. hispanicus are discussed. and widespread in the Western Palaeartic, is known for the conspicuous globular galls caused by the asexual generations on the buds of several KEY WORDS: Cynipidae, Andricus, A. kollari, A. oak species. The sexual form known hitherto, hispanicus, biological cycle, sibling species, formerly named Andricus circulans, makes small sexual form, speciation, distribution, morphology, gregarious galls on the buds of Turkey oak, A. mayeti, A. burgundus. Quercus cerris; this oak, however, is absent from the Iberian Peninsula, where on the other hand the cork oak, Q. suber, is present. Recent genetic studies show the presence of two different Resum populations or races with distribution patterns si- milar to those of Q. cerris and Q. suber. We present new biological and morphological Cicle biològic d’Andricus hispanicus (Hartig, evidence supporting the presence of a sibling 1856) una espècie bessona d’A. kollari (Hartig, species of A. kollari in the western part of its 1843) (Hymenoptera: Cynipidae) range (the Iberian Peninsula, southern France and North Africa), Andricus hispanicus n. stat.. Biological and morphological differences separating these Andricus kollari és una espècie molt comuna dis- two species from other closely related ones are tribuida a l’oest del paleartic coneguda per la given and the new sexual form is described for the gal·la globular i relativament gran de la generació first time. -
Hawai'i Landscape Plant Pest Guide: Mites and Gall-Forming Insects
Insect Pests February 2015 IP-35 Hawai‘i Landscape Plant Pest Guide: Mites And Gall-Forming Insects Arnold Hara & Ruth Niino-DuPonte Department of Plant & Environmental Protection Sciences Coconut Mite (Aceria guerreronis) Identification and Damage • Mites are microscopic and translucent, and may appear only as a silvery patch when viewed with a 10x hand lens. • Coconut mite populations peak about half way through the 12-month-long development of coconut fruit, and decline so that very few, if any, mites remain on mature coconuts. • Coconut mites disperse by wind or by being carried on insects or birds. Perianth of coconut In dense plantings, mites may be able to crawl between plants. • Mites pierce tender tissue under the perianth protecting the stem end of immature coconut fruit. As fruit matures, the damaged tissue emerges as a pale patch from the perianth. When exposed to air, the tissue develops a cork-like surface with deep cracks. • Fruits may prematurely drop or be deformed, stunted, and scarred. • The coconut mite appears to only affect coconut palms; coconut palm varieties and related species may differ in their susceptibility to this mite. Corky tissue emerges from perianth What to Do • Prune all coconuts in all stages of development to eliminate coconut mite populations. • Predatory mites and some fungi (especially under humid conditions) attack the coconut mite but may not be sufficient to control heavy infestations. • Select coconut palm varieties that are less susceptible to coconut mites. • Contact miticides need to be applied frequently and continuously to provide control. Miticides must be EPA registered for use on coconut for Closeup of corky damage human consumption of edible coconut flesh. -
The Inky Story of the Dinky Oak Gall
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln USGS Staff -- ubP lished Research US Geological Survey 2014 The nkyI Story of the Dinky Oak Gall Ken Sulak research biologist with the U.S. Geological Survey (Biological Resources), [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/usgsstaffpub Part of the Geology Commons, Oceanography and Atmospheric Sciences and Meteorology Commons, Other Earth Sciences Commons, and the Other Environmental Sciences Commons Sulak, Ken, "The nkI y Story of the Dinky Oak Gall" (2014). USGS Staff -- Published Research. 1066. http://digitalcommons.unl.edu/usgsstaffpub/1066 This Article is brought to you for free and open access by the US Geological Survey at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in USGS Staff -- ubP lished Research by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Volume 31: Number 1 > 2014 The Quarterly Journal of the Florida Native Plant Society Palmetto The Inky Story of the Dinky Oak Gall ● A Native Celebration ● The Rebirth of Cape Florida Pea galls on live oak leaves (Quercus virginiana) induced by Belonocnema treatae, a gall wasp. The Inky Story of the Dinky Oak Gall Article and photos by Ken Sulak Spring in North Florida – and all those magnificent live oaks are sporting a bright new flush of green leaves. Last year’s old clothes, those worn out leaves now lie dry and brown on the forest floor. But look closely and you will soon notice that many of those leaves are decorated with rows or clusters of little round woody galls on their underside, like little brown pearls. -
Parasitoids, Hyperparasitoids, and Inquilines Associated with the Sexual and Asexual Generations of the Gall Former, Belonocnema Treatae (Hymenoptera: Cynipidae)
Annals of the Entomological Society of America, 109(1), 2016, 49–63 doi: 10.1093/aesa/sav112 Advance Access Publication Date: 9 November 2015 Conservation Biology and Biodiversity Research article Parasitoids, Hyperparasitoids, and Inquilines Associated With the Sexual and Asexual Generations of the Gall Former, Belonocnema treatae (Hymenoptera: Cynipidae) Andrew A. Forbes,1,2 M. Carmen Hall,3,4 JoAnne Lund,3,5 Glen R. Hood,3,6 Rebecca Izen,7 Scott P. Egan,7 and James R. Ott3 Downloaded from 1Department of Biology, University of Iowa, Iowa City, IA 52242 ([email protected]), 2Corresponding author, e-mail: [email protected], 3Population and Conservation Biology Program, Department of Biology, Texas State University, San Marcos, TX 78666 ([email protected]; [email protected]; [email protected]; [email protected]), 4Current address: Science Department, Georgia Perimeter College, Decatur, GA 30034, 5Current address: 4223 Bear Track Lane, Harshaw, WI 54529, 6Current address: Department of Biological Sciences, University of Notre Dame, Galvin Life Sciences, Notre Dame, IN 46556, and 7Department of BioSciences, Anderson Biological Laboratories, Rice University, Houston, TX 77005 ([email protected], http://aesa.oxfordjournals.org/ [email protected]) Received 24 July 2015; Accepted 25 October 2015 Abstract Insect-induced plant galls are thought to provide gall-forming insects protection from predation and parasitism, yet many gall formers experience high levels of mortality inflicted by a species-rich community of insect natural enemies. Many gall-forming cynipid wasp species also display heterogony, wherein sexual (gamic) and asexual at Univ. of Massachusetts/Amherst Library on March 14, 2016 (agamic) generations may form galls on different plant tissues or plant species. -
Asian Chestnut Gall Wasp Dryocosumus Kuriphilus Yasumatsu Chestnut Species Affected: • Chinese Chestnut (C
PEST ALERT University of Missouri Extension Asian Chestnut Gall Wasp Dryocosumus kuriphilus Yasumatsu Chestnut species affected: • Chinese chestnut (C. mollissima) • Japanese chestnut (C. crenata) • European chestnut (C. sativa) • American chestnut (Castanea dentata) • Chinquapin (C. pumila) Photo: Gyorgy Csoka, Hungary Forest Research Institute, Bugwood.org Adult Asian chestnut gall wasp Distribution and hosts Tree damage The gall wasp was introduced into This insect pest lays eggs in the buds North America in 1974 on imported chest- of chestnut shoots, and galls develop on nut cuttings. A native of China, the gall the shoot tips, leaves and catkins. These wasp is also considered a major pest in galls greatly reduce nut production and Japan and Korea. suppress shoot growth. After adult insects The gall wasp has been identified in emerge, the dried, blackened galls become Georgia, Alabama, North Carolina, Vir- woody and can persist on older limbs for ginia, Maryland, Pennsylvania, Maryland, several years. In cases of severe infesta- Kentucky, Tennessee and Ohio. Although tions, interior portions of the tree canopy the gall wasp has not been found in the die and trees are killed. Midwest, it is likely to be found in addi- tional areas as detection surveys continue. Biology D. kuriphilus may be established in an area Female adult wasps, one-eighth-inch for some time before it is identified. long, lay three to five eggs in a cluster The distribution of this pest in the Unit- inside chestnut buds in early summer. ed States is primarily due to the transport Multiple adults may oviposit in a bud, of infested seedlings to new areas and the with as many as 25 eggs per bud. -
Field Release of Mompha Trithalama Meyrick (Lepidoptera: Momphidae
Field Release of Eurytoma sp. (Hymenoptera: Eurytomidae), for Biological Control of the Erythrina Gall Wasp, Quadrastichus erythrinae Kim (Hymenoptera: Eulophidae), in Hawaii Final Environmental Assessment April 7, 2008 Agency contact: Dr. Neil J. Reimer, Manager Plant Pest Control Branch Hawaii Department of Agriculture 1428 South King Street Honolulu, HI 96814-2512 Phone: (808) 973-9522 Fax: (808) 973-9533 E-mail: [email protected] This Final Environmental Assessment (FEA) and Finding of No Significant Impact (FONSI) was prepared by the HDOA Plant Quarantine Branch (approving agency) for the HDOA Plant Pest Control Branch (proposing agency) and submitted to the Office of Environmental Quality Control (OEQC), Department of Health, State of Hawaii, to comply with the provisions of Hawaii Revised Statutes, Chapter 343, Environmental Impact Statements. The appendix of this FEA contains public comment in the form of five letters of correspondence, four of which were supportive of the Erythrina Gall Wasp Project and one which required a reply to address a question raised by the writer. As a result, this FEA is unchanged from the Draft EA. I. Proposed Action An application was submitted by the Plant Pest Control Branch, Hawaii Department of Agriculture (HDOA), to the HDOA Plant Quarantine Branch, 1849 Auiki Street, Honolulu, HI 96819, for a permit to introduce Eurytoma sp. (Hymenoptera: Eurytomidae) into the State of Hawaii under the provisions of Hawaii Revised Statutes, Chapter 141, Department of Agriculture, and Chapter 150A, Plant and Non-Domestic Animal Quarantine. Eurytoma sp. will be used to control the erythrina gall wasp (EGW), Quadrastichus erythrinae Kim, an invasive eulophid wasp that has devastated endemic and introduced erythrina trees in natural and landscaped areas in Hawaii. -
Erythrina Gall Wasp
State of Hawaii New Pest Advisory DEPARTMENT OF AGRICULTURE No. 05-03 Updated December 2008 Erythrina Gall Wasp Quadrastichus erythrinae Kim (Hymenoptera: Eulophidae) Ronald A. Heu, Dick M. Tsuda*, Walter T. Nagamine, Juliana A. Yalemar and M. Tremblay Troy H. Suh Figure 1. Enlarged photo of an adult female erythrina gall wasp. Actual length of the female is 1.5 mm. The adult male wasp, not shown, measures 1.0 mm. Introduction. Samples of gall-damaged leaves and stems of the coral tree, Erythrina variegata L., were first collected in Manoa, Oahu, on April 19, 2005, by a University of Hawaii graduate student. The galls were found to have been induced by the larvae of a tiny wasp which was subsequently identified as the erythrina gall wasp (EGW), Quadrastichus erythrinae Kim (family Eulophidae) by J. La Salle of the Commonwealth Scientific and Industrial Research Organization (CSIRO) in Australia. R. Heu Figure 2. Erythrina variegata leaves exhibiting light gall wasp Erythrina variegata, with its bright red flowers, is damage (left) compared with undamaged leaves (right). also known as tigers claw, Indian coral tree, and wiliwili-haole. It is a common landscape tree in Hawaii. A tall, columnar form of E. variegata, “Tropic Coral,” known locally as “tall erythrina” or “tall wiliwili,” is also used as a windbreak for soil and water conservation and for planting around farmsteads (Rotar et al. 1986). R. Heu T. Suh Figure 3. Erythrina petioles Figure 4. “Tall erythrina” * College of Tropical Agriculture and Human Resources and leaflets exhibiting severe trees with severe gall (CTAHR), University of Hawaii at Manoa gall wasp damage. -
Research Article Population Dynamics of Native Parasitoids Associated with the Asian Chestnut Gall Wasp (Dryocosmus Kuriphilus) in Italy
Hindawi Psyche Volume 2018, Article ID 8078049, 13 pages https://doi.org/10.1155/2018/8078049 Research Article Population Dynamics of Native Parasitoids Associated with the Asian Chestnut Gall Wasp (Dryocosmus kuriphilus) in Italy Tiziana Panzavolta ,1 Francesco Croci,1 Matteo Bracalini ,1 George Melika,2 Stefano Benedettelli,1 Guido Tellini Florenzano,1 and Riziero Tiberi1 1 Department of Agrifood Production and Environmental Sciences, University of Florence, Via Maragliano 77, 50144 Florence, Italy 2Plant Health and Molecular Biology Laboratory, National Food Chain Safety Ofce, Directorate of Plant Protection, Soil Conservation and Agri-Environment, Budaorsi¨ Str. 141-145, Budapest 1118, Hungary Correspondence should be addressed to Tiziana Panzavolta; [email protected] Received 30 November 2017; Revised 18 January 2018; Accepted 8 February 2018; Published 13 March 2018 Academic Editor: Juan Corley Copyright © 2018 Tiziana Panzavolta et al. Tis is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Native parasitoids may play an important role in biological control. Tey may either support or hinder the efectiveness of introduced nonnative parasitoids released for pest control purposes. Results of a three-year survey (2011–2013) of the Asian chestnut gall wasp (ACGW) Dryocosmus kuriphilus Yasumatsu (Hymenoptera: Cynipidae) populations and on parasitism rates by native indigenous parasitoids (a complex of chalcidoid hymenopterans) in Italian chestnut forests are given. Changes in D. kuriphilus gall size and phenology were observed through the three years of study. A total of 13 species of native parasitoids were recorded, accounting for fuctuating parasitism rates. -
Evolution of the Insects
CY501-C11[407-467].qxd 3/2/05 12:56 PM Page 407 quark11 Quark11:Desktop Folder:CY501-Grimaldi:Quark_files: But, for the point of wisdom, I would choose to Know the mind that stirs Between the wings of Bees and building wasps. –George Eliot, The Spanish Gypsy 11HHymenoptera:ymenoptera: Ants, Bees, and Ants,Other Wasps Bees, and The order Hymenoptera comprises one of the four “hyperdi- various times between the Late Permian and Early Triassic. verse” insectO lineages;ther the others – Diptera, Lepidoptera, Wasps and, Thus, unlike some of the basal holometabolan orders, the of course, Coleoptera – are also holometabolous. Among Hymenoptera have a relatively recent origin, first appearing holometabolans, Hymenoptera is perhaps the most difficult in the Late Triassic. Since the Triassic, the Hymenoptera have to place in a phylogenetic framework, excepting the enig- truly come into their own, having radiated extensively in the matic twisted-wings, order Strepsiptera. Hymenoptera are Jurassic, again in the Cretaceous, and again (within certain morphologically isolated among orders of Holometabola, family-level lineages) during the Tertiary. The hymenopteran consisting of a complex mixture of primitive traits and bauplan, in both structure and function, has been tremen- numerous autapomorphies, leaving little evidence to which dously successful. group they are most closely related. Present evidence indi- While the beetles today boast the largest number of cates that the Holometabola can be organized into two major species among all orders, Hymenoptera may eventually rival lineages: the Coleoptera ϩ Neuropterida and the Panorpida. or even surpass the diversity of coleopterans (Kristensen, It is to the Panorpida that the Hymenoptera appear to be 1999a; Grissell, 1999).