Honey Bee Tracheal Mite, Acarapis Woodi (Rennie) (Arachnida: Acari: Tarsonemidae)1 H
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Acarapis Woodi (Rennie) and Varroa Destructor Q
Occurrence Of Honey Bee (Apis mellifera L.) Parasites Acarapis woodi (Rennie) and Varroa destructor Q. In The Region of Muğla, Turkey Msc. Duygu Şimşek*, Prof. Dr. Nevin KESKİN* *Hacettepe University, Department of Biology, Applied Biology Section, Ankara-TURKEY e-mail:[email protected] INTRODUCTION Another mite which causes a disease in adult honeybees is Acarapis woodi. According to the some studies carried in different periods between the years 1988-2003, there is no evidence for A. woodi which has This study was carried out to determine the occurrence of honey bee (Apis mellifera L.) parasites Acarapis been spread out in Balkans in recent years (3, 7). However, this parasite was detected in a country- woodi (Rennie) and Varroa destructor in the province of Muğla which has 17% of the hives and governs %80- wide study which was carried out with molecular techniques by Hacettepe University Bee Health Laboratory in 2005 (12). In this study, there is no evidence for A. woodi existence in samples according to the 85 of the honey export of our country. microscopic(Figure 3) and molecular assays. Varroa destructor Q (Acari, Varroidae) is a haemolymph-sucking parasite of European honey bees (9). The parasite may directly (haemolymph-sucking) and indirectly (as a vector of bacterial, fungal and viral diseases) affect the type and prevalence of honey bee pathogens causing mortality in infested colonies (2). It can be found on adult bees, on the brood and in hive debris. Adult females are a reddish colored oval-flat bodied and measured 1.1 mm long x 1.5 mm wide. -
Great Lakes Entomologist
Vol. 28, No.3 &4 Fall/Winter 1995 THE GREAT LAKES ENTOMOLOGIST PUBLISHED BY THE MICHIGAN ENTOMOLOGICAL SOCIETY THE GREAT LAKES ENTOMOLOGIST Published by the Michigan Entomological Society Volume 28 No.3 & 4 ISSN 0090-0222 TABLE OF CONTENTS Temperature effects on development of three cereal aphid porasitoids {Hymenoptera: Aphidiidael N. C. Elliott,J. D. Burd, S. D. Kindler, and J. H. Lee........................... .............. 199 Parasitism of P/athypena scabra (Lepidoptera: Noctuidael by Sinophorus !eratis (Hymenoptera: Ichneumonidae) David M. Pavuk, Charles E. Williams, and Douglas H. Taylor ............. ........ 205 An allometric study of the boxelder bug, Boiseo Irivillata (Heteroptera: Rhopolidoe) Scott M. Bouldrey and Karin A. Grimnes ....................................... ..... 207 S/aferobius insignis (Heleroptera: Lygaeidael: association with granite ledges and outcrops in Minnesota A. G. Wheeler, Jr. .. ...................... ....................... ............. ....... 213 A note on the sympotric collection of Chymomyza (Dipiero: Drosophilidael in Virginio's Allegheny Mountains Henretta Trent Bond ................ .. ............................ .... ............ ... ... 217 Economics of cell partitions and closures produced by Passa/oecus cuspidafus (Hymenoptera: Sphecidael John M. Fricke.... .. .. .. .. .. .. .. .. .. .. .. .. 221 Distribution of the milliped Narceus american us annularis (Spirabolida: Spirobolidae) in Wisconsin Dreux J. Watermolen. ................................................................... 225 -
Management of Arthropod Pathogen Vectors in North America: Minimizing Adverse Effects on Pollinators
Journal of Medical Entomology, 2017, 1–13 doi: 10.1093/jme/tjx146 Forum Forum Management of Arthropod Pathogen Vectors in North America: Minimizing Adverse Effects on Pollinators Howard S. Ginsberg,1,2 Timothy A. Bargar,3 Michelle L. Hladik,4 and Charles Lubelczyk5 1USGS Patuxent Wildlife Research Center, University of Rhode Island, RI Field Station, Woodward Hall – PSE, Kingston, RI 02881 ([email protected]), 2Corresponding author, e-mail: [email protected], 3USGS Wetland and Aquatic Research Center, 7920 NW 71st St., Gainesville, FL 32653 ([email protected]), 4USGS California Water Science Center, 6000 J St., Placer Hall, Sacramento, CA 95819 ([email protected]), and 5Maine Medical Center Research Institute, Vector-Borne Disease Laboratory, 81 Research Dr., Scarborough, ME 04074 ([email protected]) Subject Editor: Lars Eisen Received 26 April 2017; Editorial decision 19 June 2017 Abstract Tick and mosquito management is important to public health protection. At the same time, growing concerns about declines of pollinator species raise the question of whether vector control practices might affect pollinator populations. We report the results of a task force of the North American Pollinator Protection Campaign (NAPPC) that examined potential effects of vector management practices on pollinators, and how these pro- grams could be adjusted to minimize negative effects on pollinating species. The main types of vector control practices that might affect pollinators are landscape manipulation, biocontrol, and pesticide applications. Some current practices already minimize effects of vector control on pollinators (e.g., short-lived pesticides and application-targeting technologies). Nontarget effects can be further diminished by taking pollinator protection into account in the planning stages of vector management programs. -
Life History of the Honey Bee Tracheal Mite (Acari: Tarsonemidae)
ARTHROPOD BIOLOGY Life History of the Honey Bee Tracheal Mite (Acari: Tarsonemidae) JEFFERY S. PETTIS1 AND WILLIAM T. WILSON Honey Bee Research Unit, USDA-ARS, 2413 East Highway 83, Weslaco, TX 78596 Ann. Entomol. Soc. Am. 89(3): 368-374 (1996) ABSTRACT Data on the seasonal reproductive patterns of the honey bee tracheal mite, Acarapis woodi (Rennie), were obtained by dissecting host honey bees, Apis mellifera L., at intervals during their life span. Mite reproduction normally was limited to 1 complete gen- eration per host bee, regardless of host life span. However, limited egg laying by foundress progeny was observed. Longer lived bees in the fall and winter harbored mites that reproduced for a longer period than did mites in bees during spring and summer. Oviposition rate was relatively uniform at =0.85 eggs per female per day during the initial 16 d of adult bee life regardless of season. In all seasons, peak mite populations occurred in bees =24 d old, with egg laying declining rapidly beyond day 24 in spring and summer bees but more slowly in fall and winter bees. Stadial lengths of eggs and male and female larvae were 5, 4, and 5 d, respectively. Sex ratio ranged from 1.15:1 to 2.01:1, female bias, but because males are not known to migrate they would have been overestimated in the sampling scheme. Fecundity was estimated to be =21 offspring, assuming daughter mites laid limited eggs in tracheae before dispersal. Mortality of adult mites increased with host age; an estimate of 35 d for female mite longevity was indirectly obtained. -
OVERWINTERING PERFORMANCE of HONEY BEE COLONIES HEAVILY INFESTED with ACARAPIS WOODI (RENNIE) Frank A
OVERWINTERING PERFORMANCE OF HONEY BEE COLONIES HEAVILY INFESTED WITH ACARAPIS WOODI (RENNIE) Frank A. Eischen To cite this version: Frank A. Eischen. OVERWINTERING PERFORMANCE OF HONEY BEE COLONIES HEAV- ILY INFESTED WITH ACARAPIS WOODI (RENNIE). Apidologie, Springer Verlag, 1987, 18 (4), pp.293-304. hal-00890720 HAL Id: hal-00890720 https://hal.archives-ouvertes.fr/hal-00890720 Submitted on 1 Jan 1987 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. OVERWINTERING PERFORMANCE OF HONEY BEE COLONIES HEAVILY INFESTED WITH ACARAPIS WOODI (RENNIE) Frank A. EISCHEN Department of Entomology, University of Georgia, Athens, Georgia 30602 SUMMARY Three groups of honey bee colonies (N = 30) were overwintered on a mountainside (2800 M) in northeastern Mexico. Infestation levels of Acarapis woodi in the three groups averaged 0, 28.2 and 86.0 % for the control, moderately, and heavily infested colonies, respectively. Heavily infested colonies were 28 % smaller than controls (P < 0.01) in the fall. Adjusting for this, heavily infested colonies lost significantly more bees than either the moderately infested group, or the controls (P < 0.0001). Both the moderately and heavily infested groups of bees had less brood than controls at the end of the test (P < 0.02 and P < 0.01 respectively). -
Selected Miticides for Use on Ornamental Plants1
ENH1118 Selected Miticides for Use on Ornamental Plants1 Robert H. Stamps and Lance S. Osborne2 Mites are among the most difficult arthropod Some Tarsonemid mites (family Tarsonemidae) pests to control on ornamental plants. Adult mites are smaller than even false spider mites. This family have eight legs and piercing/sucking mouthparts that includes broad and cyclamen mites. are used to suck fluids from the cells of host plants (Denmark, 1969). The first immature stage of a mite, Eriophyid mites (Eriophyidae family) are too referred to as the larva, has only six legs, like insects. small to be seen with the naked eye and include bud, The exceptions are the Eriophyid mites, which have gall, purple tea and rust mites, among others. As their four legs in all stages. Mites are not insects, but are names suggest, these mites can cause galls, rusts and more closely related to spiders and ticks. Thousands other abnormal plant growth. of species of mites feed on plants. There are other families of mites that have Spider mites, members of the Tetranychidae crop-damaging members, but the mites named above family, are perhaps the most important mite pests of are the main mite pests of ornamental plants. ornamental plants. The name, spider mites, is due to Mites of a given species can develop very the many members of this family that produce silk rapidly when temperatures, relative humidities, host webbing. Spider mites are medium-sized mites that plants and other factors are optimal. In fact, for many, feed on a wide variety of host plants from many the time to develop from an egg to an adult can be different plant families. -
WO 2012/141754 A2 18 October 2012 (18.10.2012) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2012/141754 A2 18 October 2012 (18.10.2012) P O P C T (51) International Patent Classification: Not classified CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, (21) International Application Number: HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, KR, PCT/US201 1/067150 KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, (22) International Filing Date: MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, 23 December 201 1 (23. 12.201 1) OM, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, (25) Filing Language: English TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 61/428,1 18 29 December 2010 (29. 12.2010) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, (71) Applicant (for all designated States except US) : DOW TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, AGROSCIENCES LLC [US/US]; 9330 Zionsville Road, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, Indianapolis, Indiana 46268 (US). -
Colwellcv 2018 July Copy
Curriculum Vitae Robert Knight Colwell Personal Postal Address: Department of Entomology Museum of Natural History University of Colorado Boulder, CO 80309, U.S.A. E-mail: robertkcolwell@gmailcom Homepage: http://viceroy.colorado.edu/colwell Education Ph.D. 1969 University of Michigan, Ann Arbor, MI, Ecology A.B. 1965 Harvard University, Cambridge, MA, Biology Affiliations and Professional Experience 2016-Present Adjunct Professor, Tropical Forests and People Research Centre, University of the Sunshine Coast, Sippy Downs, Queensland, Australia 2012-Present Museum Curator Adjoint in Entomology and Zoology, University of Colorado Museum of Natural History, Boulder 2014-Present Distinguished Research Professor, University of Connecticut 2014-Present Board of Trustees Distinguished Professor Emeritus, University of Connecticut 2001-2014 Board of Trustees Distinguished Professor, University of Connecticut 1989-2001 Professor, University of Connecticut 1982-1990 Professor, University of California at Berkeley 1976-1982 Associate Professor, University of California, Berkeley 1970-1976 Assistant Professor, University of California, Berkeley 2014-Present Professor e Pesquisador Visitante Especial, Universidade Federal de Goiás, Brazil 2010-Present International Collaborator, Center for Macroecology, Evolution and Climate, The Natural History Museum of Denmark, University of Copenhagen, Denmark 1983-1985 Vice Chair, Department of Zoology, U.C., Berkeley 1982 Acting Chair, Department of Zoology, U.C., Berkeley 1969-1970 Ford Postdoctoral Fellow, -
PARASITIC MITES of HONEY BEES: Life History, Implications, and Impact
Annu. Rev. Entomol. 2000. 45:519±548 Copyright q 2000 by Annual Reviews. All rights reserved. PARASITIC MITES OF HONEY BEES: Life History, Implications, and Impact Diana Sammataro1, Uri Gerson2, and Glen Needham3 1Department of Entomology, The Pennsylvania State University, 501 Agricultural Sciences and Industries Building, University Park, PA 16802; e-mail: [email protected] 2Department of Entomology, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, Rehovot 76100, Israel; e-mail: [email protected] 3Acarology Laboratory, Department of Entomology, 484 W. 12th Ave., The Ohio State University, Columbus, Ohio 43210; e-mail: [email protected] Key Words bee mites, Acarapis, Varroa, Tropilaelaps, Apis mellifera Abstract The hive of the honey bee is a suitable habitat for diverse mites (Acari), including nonparasitic, omnivorous, and pollen-feeding species, and para- sites. The biology and damage of the three main pest species Acarapis woodi, Varroa jacobsoni, and Tropilaelaps clareae is reviewed, along with detection and control methods. The hypothesis that Acarapis woodi is a recently evolved species is rejected. Mite-associated bee pathologies (mostly viral) also cause increasing losses to apiaries. Future studies on bee mites are beset by three main problems: (a) The recent discovery of several new honey bee species and new bee-parasitizing mite species (along with the probability that several species are masquerading under the name Varroa jacob- soni) may bring about new bee-mite associations and increase damage to beekeeping; (b) methods for studying bee pathologies caused by viruses are still largely lacking; (c) few bee- and consumer-friendly methods for controlling bee mites in large apiaries are available. -
Effects of Tracheal Mite Infestation on Japanese Honey Bee, Apis Cerana Japonica
J. Acarol. Soc. Jpn., 25(S1): 109-117. March 25, 2016 © The Acarological Society of Japan http://www.acarology-japan.org/ 109 Effects of tracheal mite infestation on Japanese honey bee, Apis cerana japonica Taro MAEDA* National Institute of Agrobiological Sciences, 1-2 Ohwashi, Tsukuba, Ibaraki 305-0851; Japan ABSTRACT The honey bee tracheal mite, Acarapis woodi (Acari: Tarsonemidae), is an endoparasite of honey bees. The mites feed on bee hemolymph in the tracheas of adult bees. Mite infestations cause serious damage to bee colonies. The distribution of these mites is now worldwide, from Europe to South and North America. The first recorded A. woodi infestation in the Japanese native honey bee, Apis cerana japonica, occurred in 2010. In a previous study, to determine the distribution of A. woodi in Japan, we sampled more than 350 colonies of A. cerana japonica. We found mite infestation from central to eastern Japan. On the other hand, Apis mellifera in Japan has not suffered serious mite damage. Here, to determine the effects of mite infestation on Japanese native honey bees, we investigated seasonal prevalence, mite load in the tracheal tube, and the relationship between mite prevalence and K-wing (disjointed wings). Similar to European honey bees, Japanese honey bees had a high prevalence of mite infestation in winter and a low prevalence in summer. The average mite load was about 21 or 22 mites (all stages) per trachea when all bees were infested by tracheal mites (100% mite prevalence). This mite load did not differ from that in A. mellifera. The K-wing rate was positively correlated with mite prevalence. -
Julius-Kühn-Archiv
ICP-PR Honey Bee Protection Group 1980 - 2015 The ICP-PR Bee Protection Group held its fi rst meeting in Wageningen in 1980 and over the subsequent 35 years it has become the established expert forum for discussing the risk of pesticides to bees and developing solutions how to assess and manage this risk. In recent years it has enlarged its scope of interest from honey bees to many other pollinating insects such as bumble bees. The group organises international scientifi c symposia once in every three years. These are open to everyone interested. The group tries to involve as many countries as possible, by organising symposia each time in another European country. It operates with working groups studying specifi c problems and proposing solu- 450 tions that are subsequently discussed in plenary symposia. A wide range of experts active in this fi eld drawn Julius-Kühn-Archiv from regulatory authorities, industry, universities and research institutes across the European Union (EU) and beyond participates in the discussions. Pieter A. Oomen, Jens Pistorius (Editors) The proceedings of the symposia (such as these) are being published by the Julius Kühn Archive in Germany since the 2008 symposium in Bucharest, Romania. These proceedings are also accessible on internet, e.g., the 2011 Wageningen symposium is available on http://pub.jki.bund.de/index.php/JKA/issue/view/801. Hazards of pesticides to bees For more information about the Bee Protection Group, see the ‘Statement about the mission and role of the ICPPR Bee Protection Group’ on one of the opening pages in these proceedings. -
Cyclamen Mite, Phytonemus Pallidus (Banks) (Arachnida: Acarina: Tarsonemidae)1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY-178 Cyclamen Mite, Phytonemus pallidus (Banks) (Arachnida: Acarina: Tarsonemidae)1 H. A. Denmark2 Introduction Synonymy The cyclamen mite, Phytonemus pallidus Tarsonemus pallidus Banks, 1901: 294. (Banks), (family Tarsonemidae), was first noticed in New York in 1898 and in Canada in 1908. The Tarsonemus fragariae Zimmerman, 1905: 91. cyclamen mite was described by Banks (1901) as Steneotarsonemus pallidus (Banks), Beer, Tarsonemus pallidus from leaves of greenhouse 1954: 1267. chrysanthemums at Jamaica, New York. Today, it is generally distributed throughout the country. Ewing Phytodromus pallidus (Banks), Lindquist, (1939) considered Tarsonemus fragariae Zimmermn 1987: 291. and T. destructor Reuter to be synonyms of T. pallidus Banks. Beer (1954) placed it in the genus Steneotarsonemus. However, Linquist placed in it the genus Phytodromus in 1987. Description The mites are often found on the corms of This is one of the smaller mites that attacks cyclamens in storage and are thus transported by ornamental plants. The adult female mite is yellowish trade. It has been spread on plants in unopened brown, 250µ to 260µ long, with hind legs reduced leaflets and on the tubers of cyclamen to all parts of to slender threadlike structures. The male is the world. This mite requires high humidity and approximately 75% the size of the female. On the avoids light. It overwinters in the adult stage in the adult males the fourth pair of legs are modified and temperate zone. It is widely distributed throughout are used to transport the pupae or adult females.