Redalyc.Coccidology. the Study of Scale Insects (Hemiptera: Sternorrhyncha: Coccoidea)
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Historical Biogeography of an Emergent Forest Pest, Matsucoccus Macrocicatrices
Received: 19 April 2019 | Revised: 7 August 2019 | Accepted: 12 August 2019 DOI: 10.1111/jbi.13702 RESEARCH PAPER Native or non‐native? Historical biogeography of an emergent forest pest, Matsucoccus macrocicatrices Thomas D. Whitney1,2 | Kamal J. K. Gandhi1 | Rima D. Lucardi2 1Puyallup Research and Extension Center, Washington State University, Abstract Puyallup, WA 98371, USA Aim: A historically benign insect herbivore, Matsucoccus macrocicatrices, has re‐ 2 USDA Forest Service, Southern Research cently been linked to dieback and mortality of eastern white pine (Pinus strobus L.). Station, 320 E. Green Street, Athens, GA 30602, USA Previous reports indicated that its native range was restricted to New England, USA and southeastern Canada. Now, the insect occurs throughout an area extending from Correspondence Thomas D. Whitney, Puyallup Research the putative native range, southward to Georgia, and westward to Wisconsin. Our and Extension Center, Washington State goal was to evaluate whether its current distribution was due to recent introduc‐ University, Puyallup, WA 98371, USA. Email: [email protected] tions consistent with invasion processes. We considered two hypotheses: (a) if recent expansion into adventive regions occurred, those populations would have reduced Funding information USDA Forest Service, Southern genetic diversity due to founder effect(s); alternatively (b) if M. macrocicatrices is na‐ Research Station, Grant/Award tive and historically co‐occurred with its host tree throughout the North American Number: 13‐CA‐11330129‐056 and 16‐ CS‐11330129‐045; Southern Region (8)‐ range, then populations would have greater overall genetic diversity and a population Forest Health Protection; USDA Agricultural structure indicative of past biogeographical influences. -
Ladybirds, Ladybird Beetles, Lady Beetles, Ladybugs of Florida, Coleoptera: Coccinellidae1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY-170 Ladybirds, Ladybird beetles, Lady Beetles, Ladybugs of Florida, Coleoptera: Coccinellidae1 J. H. Frank R. F. Mizell, III2 Introduction Ladybird is a name that has been used in England for more than 600 years for the European beetle Coccinella septempunctata. As knowledge about insects increased, the name became extended to all its relatives, members of the beetle family Coccinellidae. Of course these insects are not birds, but butterflies are not flies, nor are dragonflies, stoneflies, mayflies, and fireflies, which all are true common names in folklore, not invented names. The lady for whom they were named was "the Virgin Mary," and common names in other European languages have the same association (the German name Marienkafer translates Figure 1. Adult Coccinella septempunctata Linnaeus, the to "Marybeetle" or ladybeetle). Prose and poetry sevenspotted lady beetle. Credits: James Castner, University of Florida mention ladybird, perhaps the most familiar in English being the children's rhyme: Now, the word ladybird applies to a whole Ladybird, ladybird, fly away home, family of beetles, Coccinellidae or ladybirds, not just Your house is on fire, your children all gone... Coccinella septempunctata. We can but hope that newspaper writers will desist from generalizing them In the USA, the name ladybird was popularly all as "the ladybird" and thus deluding the public into americanized to ladybug, although these insects are believing that there is only one species. There are beetles (Coleoptera), not bugs (Hemiptera). many species of ladybirds, just as there are of birds, and the word "variety" (frequently use by newspaper 1. -
Zootaxa,Phylogeny and Higher Classification of the Scale Insects
Zootaxa 1668: 413–425 (2007) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2007 · Magnolia Press ISSN 1175-5334 (online edition) Phylogeny and higher classification of the scale insects (Hemiptera: Sternorrhyncha: Coccoidea)* P.J. GULLAN1 AND L.G. COOK2 1Department of Entomology, University of California, One Shields Avenue, Davis, CA 95616, U.S.A. E-mail: [email protected] 2School of Integrative Biology, The University of Queensland, Brisbane, Queensland 4072, Australia. Email: [email protected] *In: Zhang, Z.-Q. & Shear, W.A. (Eds) (2007) Linnaeus Tercentenary: Progress in Invertebrate Taxonomy. Zootaxa, 1668, 1–766. Table of contents Abstract . .413 Introduction . .413 A review of archaeococcoid classification and relationships . 416 A review of neococcoid classification and relationships . .420 Future directions . .421 Acknowledgements . .422 References . .422 Abstract The superfamily Coccoidea contains nearly 8000 species of plant-feeding hemipterans comprising up to 32 families divided traditionally into two informal groups, the archaeococcoids and the neococcoids. The neococcoids form a mono- phyletic group supported by both morphological and genetic data. In contrast, the monophyly of the archaeococcoids is uncertain and the higher level ranks within it have been controversial, particularly since the late Professor Jan Koteja introduced his multi-family classification for scale insects in 1974. Recent phylogenetic studies using molecular and morphological data support the recognition of up to 15 extant families of archaeococcoids, including 11 families for the former Margarodidae sensu lato, vindicating Koteja’s views. Archaeococcoids are represented better in the fossil record than neococcoids, and have an adequate record through the Tertiary and Cretaceous but almost no putative coccoid fos- sils are known from earlier. -
The <I>Matsucoccus</I> Cockerell, 1909 of Florida (Hemiptera
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 9-30-2020 The Matsucoccus Cockerell, 1909 of Florida (Hemiptera: Coccomorpha: Matsucoccidae): Potential pests of Florida pines Muhammad Z. Ahmed Charles H. Ray Matthew R. Moore Douglass R. Miller Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons 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. InsectaA journal of world insect systematics Mundi 0810 The Matsucoccus Cockerell, 1909 of Florida Page Count: 31 (Hemiptera: Coccomorpha: Matsucoccidae): Potential pests of Florida pines Muhammad Z. Ahmed Florida State Collection of Arthropods Division of Plant Industry, Florida Department of Agriculture and Consumer Services 1911 SW 34th Street Gainesville, FL 32608, USA [email protected] Charles H. Ray Department of Entomology and Plant Pathology Auburn University Museum of Natural History Room 301, Funchess Hall Auburn University, AL 36849, USA Matthew R. Moore Molecular Diagnostics Laboratory Division of Plant Industry, Florida Department of Agriculture and Consumer Services 1911 SW 34th Street Gainesville, FL 32608, USA Douglass R. Miller Florida State Collection of Arthropods Division of Plant Industry, Florida Department of Agriculture and Consumer Services 1911 SW 34th Street Gainesville, FL 32608, USA Date of issue: October 30, 2020 Center for Systematic Entomology, Inc., Gainesville, FL Ahmed MZ, Ray CH, Moore MR, Miller DR. -
Differences in the Sugar Composition of the Honeydew of Polyphagous
NOTE Eur. J. Entomol. 108: 705–709, 2011 http://www.eje.cz/scripts/viewabstract.php?abstract=1671 ISSN 1210-5759 (print), 1802-8829 (online) Differences in the sugar composition of the honeydew of polyphagous brown soft scale Coccus hesperidum (Hemiptera: Sternorrhyncha: Coccoidea) feeding on various host plants KATARZYNA GOLAN 1 and AGNIESZKA NAJDA2 1Department of Entomology, University of Life Sciences in Lublin, LeszczyĔskiego 7, 20-069 Lublin, Poland; e-mail: [email protected] 2 Department of Vegetable and Medicinal Plants, University of Life Sciences in Lublin, LeszczyĔskiego 58, 20-068 Lublin, Poland Key words. Coccoidea, Coccus hesperidum, brown scale insects, honeydew, host plants, soft scale, sugar composition Abstract. Plant chemical composition is an important determinant of host plant-insect interactions. For many insects sugars are the main factors determining the acceptability of a plant. This study investigated changes in plant chemical composition and differences in sugar composition of different host plants induced by the feeding of Coccus hesperidum L. (Hemiptera: Sternorrhyncha: Coccoi- dea). Present in plant extracts and honeydew there were three monosaccharide sugars: glucose, fructose and arabinose, and one disaccharide – sucrose. Arabinose was only found in extracts of Ficus benjamina plants. The sugar content of the honeydew was greater than in the extracts of control plants and lower than that in the extracts of infested plants. The honeydew collected from C. hesperidum feeding on the three plant species differed significantly in sugar content. Extracts of coccid infested plants of the three species used in this study contained more sugar than the un-infested control plants. The results show that honeydew composition of scale insects differ and the differences reflect the chemical composition of the host plants. -
Objective Forest Management of Eastern Mediterranean Pinus Brutia
Dissertationes Forestales 170 Growth and yield modelling for optimal multi- objective forest management of eastern Mediterranean Pinus brutia Sergio de Miguel Magaña School of Forest Sciences Faculty of Science and Forestry University of Eastern Finland Academic dissertation To be presented, with the permission of the Faculty of Science and Forestry of the University of Eastern Finland, for public criticism in auditorium M102 of the University of Eastern Finland, Yliopistokatu 7, Joensuu on 21st February 2014 at 12 o’clock noon. 2 Title of dissertation: Growth and yield modelling for optimal multi-objective forest management of eastern Mediterranean Pinus brutia. Author: Sergio de Miguel Magaña Dissertationes Forestales 170 http://dx.doi.org/10.14214/df.170 Thesis supervisor: Prof. Timo Pukkala School of Forest Sciences, Faculty of Science and Forestry, University of Eastern Finland Pre-examiners: Prof. Harold Burkhart Department of Forest Resources and Environmental Conservation, Virginia Polytechnic Institute and State University, Blacksburg, United States Dr. Jari Miina Finnish Forest Research Institute, Eastern Finland Regional Unit, Joensuu, Finland Opponent: Prof. Jerome K. Vanclay Forest Research Centre, School of Environment, Science and Engineering, Southern Cross University, Lismore, Australia ISSN 1795-7389 (online) ISBN 978-951-651-430-0 (pdf) ISSN 2323-9220 (print) ISBN 978-951-651-429-4 (paperback) 2014 Publishers: Finnish Society of Forest Science Finnish Forest Research Institute Faculty of Agriculture and Forestry of the University of Helsinki School of Forest Sciences of the University of Eastern Finland Editorial Office: The Finnish Society of Forest Science P.O. Box 18, FI-01301 Vantaa, Finland http://www.metla.fi/dissertationes 3 de Miguel Magaña, S. -
A New Pupillarial Scale Insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in Coastal New South Wales, Australia
Zootaxa 4117 (1): 085–100 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4117.1.4 http://zoobank.org/urn:lsid:zoobank.org:pub:5C240849-6842-44B0-AD9F-DFB25038B675 A new pupillarial scale insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in coastal New South Wales, Australia PENNY J. GULLAN1,3 & DOUGLAS J. WILLIAMS2 1Division of Evolution, Ecology & Genetics, Research School of Biology, The Australian National University, Acton, Canberra, A.C.T. 2601, Australia 2The Natural History Museum, Department of Life Sciences (Entomology), London SW7 5BD, UK 3Corresponding author. E-mail: [email protected] Abstract A new scale insect, Aolacoccus angophorae gen. nov. and sp. nov. (Eriococcidae), is described from the bark of Ango- phora (Myrtaceae) growing in the Sydney area of New South Wales, Australia. These insects do not produce honeydew, are not ant-tended and probably feed on cortical parenchyma. The adult female is pupillarial as it is retained within the cuticle of the penultimate (second) instar. The crawlers (mobile first-instar nymphs) emerge via a flap or operculum at the posterior end of the abdomen of the second-instar exuviae. The adult and second-instar females, second-instar male and first-instar nymph, as well as salient features of the apterous adult male, are described and illustrated. The adult female of this new taxon has some morphological similarities to females of the non-pupillarial palm scale Phoenicococcus marlatti Cockerell (Phoenicococcidae), the pupillarial palm scales (Halimococcidae) and some pupillarial genera of armoured scales (Diaspididae), but is related to other Australian Myrtaceae-feeding eriococcids. -
BIOLOGICAL CONTROL of CITRUS SCALE PESTS in JAPAN M. Takagi Faculty of Agriculture, Kyushu University, Fukuoka, Japan
__________________________________________ Biological control of citrus scale pests in Japan 351 BIOLOGICAL CONTROL OF CITRUS SCALE PESTS IN JAPAN M. Takagi Faculty of Agriculture, Kyushu University, Fukuoka, Japan INTRODUCTION There were no serious citrus pests in Japan before 1867 because there was little international trade in Japan when it was a closed country during the Edo period. After Japan opened up as a country, many adventive agricultural pests were accidentally introduced. Many serious citrus scale pests were intro- duced into Japan around 1900. Classical biological control was very effective against those adventive pests, which are still well controlled by introduced natural enemies. However, the history of these biological control projects varies significantly among these pests. The first attempt to introduce foreign natural enemies into Japan to control a citrus pest was the importation of the vedalia beetle, Rodolia cardinalis (Mulsant), against the cottony cushion scale, Icerya purchasi Maskell. This attempt was very quickly carried out and was successful, as in many other countries. The second successful project was the biological control of the red wax scale, Ceroplastes rubens Maskell, by the encrytid, Anicetus beneficus Ishii et Yasumatu. In this case, the effective natural enemy invaded Japan without any intentional introduction from foreign countries. The last successful citrus scale biological control project in Japan was of arrowhead scale, Unaspis yanonensis (Kuwana), by the aphelinids, Aphytis yanonensis DeBach et Rosen and Coccobius fulvus (Compere et Annecke). In this case, it was nearly 80 years between the pest’s invasion and the successful introduction of the effective natural enemies. Here I review the history of the accidental introduction of these citrus scale pests and the efforts and successes of the classical biological control of these adventive citrus scale pests in Japan. -
Giant Pine Scale Description Giant Pine Scale (Marchalina Hellenica) Is a Large Scale Insect That Reaches a Length of 8–19 Mm and 3–5 Mm Wide
Fact sheet Giant pine scale Description Giant pine scale (Marchalina hellenica) is a large scale insect that reaches a length of 8–19 mm and 3–5 mm wide. The pest feeds on the sap of various conifers and, while feeding, secretes a white waxy substance. The insect feeds mostly on the lower trunk of infested SOFTWOOD SPECIES trees but will also feed on branches or, in some cases, above ground roots. This species originates from the Mediterranean but has been found in Australia in Melbourne and Adelaide. Angus Carnegie, NSW DPI Primary hosts Waxy secretions caused by the giant pine scale Giant pine scale feeds exclusively on plants of the family Pinaceae. Overseas host records include the following genera and species: • Firs: Greek fir (Abies cephalonica), Caucasian fir (A. nordmanniana), • Spruces: Engelmann spruce (Picea engelmannii), Oriental spruce (P. orientalis) • Pines: Turkish pine (Pinus brutia), Aleppo pine (P. halepensis), Caucasian pine (P. kochiana, P. sosnowskyi), Corsican pine (P. laricio), Black pine (P. nigra), Stone pine (P. pinea), Scots pine (P. sylvestris). In Australia, giant pine scale has been found on Aleppo Battisti, Universita di Padova, Bugwood.org Andrea pine (Pinus halapensis), stone pine (Pinus pinea) and Adult giant pine scale radiata or Monterey pine (Pinus radiata). Symptoms Giant pine scale produces a distinctive white, cotton- like, wax secretion, which stands out within the cracks of the dark trunks and branches of host trees. The insect prefers the lower part of the tree and mainly occurs on the trunk, but it may also be found on branches well up in the canopy, and even on exposed roots. -
COCCUS HESPERIDUM ) INFESTING Holly on VANCOUVER ISLAND
THE SOFT SCALE (COCCUS HESPERIDUM ) INFESTING HOllY ON VANCOUVER ISLAND ( A Preliminary Report ) Tile :,,,ft ;.;cale ( Coccus hesperidum ( L. )) ha,; iJec\J111e \ery pre\- alent o n holly tre es in many part:; PI' the :,() uthe rn Yanc(lu\-e r I sland d istrict durin'g t h e past :-e,;r. It \\' <1" Ilrst noticed in the I'ic inity of Victor ia, B.C., during Febru ary, ] 93 :::: ; s pecimens \\'ere iUr\\'arcled t( I the D ivision of Entolllolog-y at Otta\\'a. and \\-e re s ub seCj ue ntly deter mined Ill- 1)1'. Tlarold :\ I(l rrisun o i \\'ashin~n\ln. D.C. ,-\ d clitional IlOlh' trees \\ -~ re e:'-: alllineci during the c (; urse of the 1 0:],'1 season \yhen w'e o bsen'ed the soft scale spreaciing Yer,\- r apid ly, .\ black fung-us ( pre)]) ably Meliola camelliae Catt. \\'ith w hi c h thi:, scale is as,;ociated ) \\-as fO llnd to be present \\'here\'er the scale inie,;tatiun s occurrecl. Speci men s \\'Cre fo und a s far n o rth a s Duncan, The e:'tahli slllllent I Ii the ""it scale and t h e :' o ut,\-- lll uld fungus (I n hull), in I\riti,;h Columhia is it seri, IUS menace to the [>1'Ociuction and e:'-: pll rtatio n of ho lly f()r th e Ch r istmas season. Plant quarantine,; re o;t ricting the free 111(J\ elllent (I f the :'i cale-infested 11CJIh', foc u ,;,; ed t h e attention of t h e cOlll111e rc ial grll \\'er:, upo n th is pC'st ;lnd created an immediate n eecl fo r inf' lrlllati( ln u po n its life hahits and c() ntr,']. -
Records of the Hawaii Biological Survey for 1996
Records of the Hawaii Biological Survey for 1996. Bishop Museum Occasional Papers 49, 71 p. (1997) RECORDS OF THE HAWAII BIOLOGICAL SURVEY FOR 1996 Part 2: Notes1 This is the second of 2 parts to the Records of the Hawaii Biological Survey for 1996 and contains the notes on Hawaiian species of protists, fungi, plants, and animals includ- ing new state and island records, range extensions, and other information. Larger, more comprehensive treatments and papers describing new taxa are treated in the first part of this Records [Bishop Museum Occasional Papers 48]. Foraminifera of Hawaii: Literature Survey THOMAS A. BURCH & BEATRICE L. BURCH (Research Associates in Zoology, Hawaii Biological Survey, Bishop Museum, 1525 Bernice Street, Honolulu, HI 96817, USA) The result of a compilation of a checklist of Foraminifera of the Hawaiian Islands is a list of 755 taxa reported in the literature below. The entire list is planned to be published as a Bishop Museum Technical Report. This list also includes other names that have been applied to Hawaiian foraminiferans. Loeblich & Tappan (1994) and Jones (1994) dis- agree about which names should be used; therefore, each is cross referenced to the other. Literature Cited Bagg, R.M., Jr. 1980. Foraminifera collected near the Hawaiian Islands by the Steamer Albatross in 1902. Proc. U.S. Natl. Mus. 34(1603): 113–73. Barker, R.W. 1960. Taxonomic notes on the species figured by H. B. Brady in his report on the Foraminifera dredged by HMS Challenger during the years 1873–1876. Soc. Econ. Paleontol. Mineral. Spec. Publ. 9, 239 p. Belford, D.J. -
HOST PLANTS of SOME STERNORRHYNCHA (Phytophthires) in NETHERLANDS NEW GUINEA (Homoptera)
Pacific Insects 4 (1) : 119-120 January 31, 1962 HOST PLANTS OF SOME STERNORRHYNCHA (Phytophthires) IN NETHERLANDS NEW GUINEA (Homoptera) By R. T. Simon Thomas DEPARTMENT OF ECONOMIC AFFAIRS, HOLLANDIA In this paper, I list 15 hostplants of some Phytophthires of Netherlands New Guinea. Families, genera within the families and species within the genera are mentioned in alpha betical order. The genera and the specific names of the insects are printed in bold-face type, those of the plants are in italics. The locality, where the insects were found, is printed after the host plants. Then follows the date of collection and finally the name of the collector1 in parentheses. I want to acknowledge my great appreciation for the identification of the Aphididae to Mr. D. Hille Ris Lambers and of the Coccoidea to Dr. A. Reyne. Aphididae Cerataphis variabilis Hrl. Cocos nucifera Linn.: Koor, near Sorong, 26-VII-1961 (S. Th.). Longiunguis sacchari Zehntner. Andropogon sorghum Brot.: Kota Nica2 13-V-1959 (S. Th.). Toxoptera aurantii Fonsc. Citrus sp.: Kota Nica, 16-VI-1961 (S. Th.). Theobroma cacao Linn.: Kota Nica, 19-VIII-1959 (S. Th.), Amban-South, near Manokwari, 1-XII- 1960 (J. Schreurs). Toxoptera citricida Kirkaldy. Citrus sp.: Kota Nica, 16-VI-1961 (S. Th.). Schizaphis cyperi v. d. Goot, subsp, hollandiae Hille Ris Lambers (in litt.). Polytrias amaura O. K.: Hollandia, 22-V-1958 (van Leeuwen). COCCOIDEA Aleurodidae Aleurocanthus sp. Citrus sp.: Kota Nica, 16-VI-1961 (S. Th.). Asterolecaniidae Asterolecanium pustulans (Cockerell). Leucaena glauca Bth.: Kota Nica, 8-X-1960 (S. Th.). 1. My name, as collector, is mentioned thus: "S.