Chalcidoidea: Encyrtidae) from Received: 16-03-2019 Accepted: 20-04-2019 Bihar, India
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Lepidoptera, Zygaenidae
©Ges. zur Förderung d. Erforschung von Insektenwanderungen e.V. München, download unter www.zobodat.at _______Atalanta (Dezember 2003) 34(3/4):443-451, Würzburg, ISSN 0171-0079 _______ Natural enemies of burnets (Lepidoptera, Zygaenidae) 2nd Contribution to the knowledge of hymenoptera paraziting burnets (Hymenoptera: Braconidae, Ichneumonidae, Chaleididae) by Tadeusz Kazmierczak & J erzy S. D ^browski received 18.VIII.2003 Abstract: New trophic relationships between Braconidae, Ichneumonidae, Chaleididae, Pteromalidae, Encyrtidae, Torymidae, Eulophidae (Hymenoptera) and burnets (Lepidoptera, Zygaenidae) collected in selected regions of southern Poland are considered. Introduction Over 30 species of insects from the family Zygaenidae (Lepidoptera) occur in Central Europe. The occurrence of sixteen of them was reported in Poland (D/^browski & Krzywicki , 1982; D/^browski, 1998). Most of these species are decidedly xerothermophilous, i.e. they inhabit dry, open and strongly insolated habitats. Among the species discussed in this paperZygaena (Zygaena) angelicae O chsenheimer, Z. (Agrumenia) carniolica (Scopoli) and Z (Zygaena) loti (Denis & Schiffermuller) have the greatest requirements in this respect, and they mainly live in dry, strongly insolated grasslands situated on lime and chalk subsoil. The remaining species occur in fresh and moist habitats, e. g. in forest meadows and peatbogs. Due to overgrowing of the habitats of these insects with shrubs and trees as a result of natural succession and re forestation, or other antropogenic activities (urbanization, land reclamation) their numbers decrease, and they become more and more rare and endangered. During many years of investigations concerning the family Zygaenidae their primary and secondary parasitoids belonging to several families of Hymenoptera were reared. The host species were as follows: Adscita (Adscita) statices (L.), Zygaena (Mesembrynus) brizae (Esper), Z (Mesembrynus) minos (Denis & Schiffermuller), Z. -
Hymenoptera) of Meghalaya with Special Reference to Encyrtidae, Mymaridae and Aphelinidae
Journal of Biological Control, 29(2): 49-61, 2015 Research Article Additions to the Chalcidoidea (Hymenoptera) of Meghalaya with special reference to Encyrtidae, Mymaridae and Aphelinidae A. RAMESHKUMAR*, J. POORANI and V. NAVEEN Division of Insect Systematics, ICAR-National Bureau of Agricultural Insect Resources, H. A. Farm post, Bellary road, Hebbal, Bangalore - 560024, Karnataka. *Corresponding author E-mail: [email protected] ABSTRACT: Encyrtidae, Mymaridae and Aphelinidae were surveyed from Ri-Bhoi, Jaintia hills, East Khasi hills, and West Khasi hills districts of Meghalaya in 2013. New distribution records of 55 genera and 61 species of encyrtids, mymarids aphelinids and eucharitids for Meghalaya state are documented. KEY WORDS: Encyrtidae, Mymaridae, Aphelinidae, distributional records, India, Meghalaya (Article chronicle: Received: 01-06-2015; Revised: 21-06-2015; Accepted: 23-06-2015) INTRODUCTION composite images were obtained from image stacks using Combine ZP. The images were arranged in plates in Adobe Studies on the Chalcidoidea fauna of Meghalaya are Photoshop Elements 11. very limited and the state has not been systematically sur- veyed for encyrtids, mymarids and aphelinids though they RESULTS AND DISCUSSION play an important role in natural and applied biological control. Hayat and his co-workers have contributed to the During the survey, 950 specimens of chalcidoids and known fauna of Meghalaya (Hayat, 1998; Hayat, 2006; Ka- other parasitoids were collected. Twenty two species repre- zmi and Hayat, 2012; Zeya and Hayat, 1995). We surveyed senting 16 genera of mymarids, 30 species representing 28 four districts of Meghalaya in 2013 for Chalcidoidea with genera of encyrtids, 10 genera and 8 species of aphelinids particular reference to Encyrtidae, Aphelinidae and My- and Orasema initiator Kerrich of eucharitid are reported maridae and documented several taxa new to the state. -
Chalcid Forum Chalcid Forum
ChalcidChalcid ForumForum A Forum to Promote Communication Among Chalcid Workers Volume 23. February 2001 Edited by: Michael E. Schauff, E. E. Grissell, Tami Carlow, & Michael Gates Systematic Entomology Lab., USDA, c/o National Museum of Natural History Washington, D.C. 20560-0168 http://www.sel.barc.usda.gov (see Research and Documents) minutes as she paced up and down B. sarothroides stems Editor's Notes (both living and partially dead) antennating as she pro- gressed. Every 20-30 seconds, she would briefly pause to Welcome to the 23rd edition of Chalcid Forum. raise then lower her body, the chalcidoid analog of a push- This issue's masthead is Perissocentrus striatululus up. Upon approaching the branch tips, 1-2 resident males would approach and hover in the vicinity of the female. created by Natalia Florenskaya. This issue is also Unfortunately, no pre-copulatory or copulatory behaviors available on the Systematic Ent. Lab. web site at: were observed. Naturally, the female wound up leaving http://www.sel.barc.usda.gov. We also now have with me. available all the past issues of Chalcid Forum avail- The second behavior observed took place at Harshaw able as PDF documents. Check it out!! Creek, ~7 miles southeast of Patagonia in 1999. Jeremiah George (a lepidopterist, but don't hold that against him) and I pulled off in our favorite camping site near the Research News intersection of FR 139 and FR 58 and began sweeping. I knew that this area was productive for the large and Michael W. Gates brilliant green-blue O. tolteca, a parasitoid of Pheidole vasleti Wheeler (Formicidae) brood. -
Hymenoptera: Ichneumonidae) from Guilan Province, Northern Iran
A contribution to the knowledge of the Ichneumon wasps (Hymenoptera: Ichneumonidae) from Guilan Province, Northern Iran Hassan Ghahari & Reijo Jussila Abstract. In a total of 28 ichneumonid species from 22 genera and 6 subfamilies (Cremastinae, Cryptinae, Ichneumoninae, Pimplinae, Rhyssinae and Tryphoninae) were collected from Guilan province, northern Iran. Of these, one species Schizopyga podagrica Gravenhorst is new record for Iran. Samenvatting. Een bijdrage tot de kennis van de Ichenomindae (Hymenoptera) van de provincie Guilan, Noord-Iran In het totaal werden 28 soorten Ichneumonidae behorend tot 22 genera en 6 subfamilies (Cremastinae, Cryptinae, Ichneumoninae, Pimplinae, Rhyssinae en Tryphoninae) verzameld in de provincie Guilan, Noord-Iran. Schizopyga podagrica Gravenhorst is nieuw voor Iran. Résumé. Contribution à la connaissance des Ichneumonidae (Hymenoptera) de la province de Guilan, Iran septentrional Au total 28 espèces d'Ichneumonidae furent capturées dans la province de Guilan, Iran septentrional, appartenant à 22 genres et 6 sous-familles (Cremastinae, Cryptinae, Ichneumoninae, Pimplinae, Rhyssinae et Tryphoninae). Schizopyga podagrica Gravenhorst est mentionné ici pour la première fois d'Iran. Keywords: Ichneumonidae – Fauna – Faunistics – Guilan Province – Iran. Ghahari H.: Department of Entomology, Islamic Azad University, Science and Research Branch, Tehran, Iran. [email protected] Jussila R.: Zoological Museum, Section of Biodiversity and Environmental Sciences, Department of Biology, FI-20014 University of Turku, Finland. Introduction Afrotropical region (Yu 1998). Ichneumonids utilise a diverse array of insects and arachnids as their hosts and The Ichneumonidae are one of the most species-rich play an essential role in the normal functioning of most families of all organisms with an estimated 60,000 ecosystems, underlining the need to inventory their species in the world (Townes 1969). -
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. -
Diversity of Parasitoid Wasps in Conventional and Organic Guarana (Paullinia Cupana Var
ACTA AMAZONICA http://dx.doi.org/10.1590/1809-4392201804560 ORIGINAL ARTICLE Diversity of parasitoid wasps in conventional and organic guarana (Paullinia cupana var. sorbilis) cultivation areas in the Brazilian Amazon Karine SCHOENINGER1* , Jorge L.P. SOUZA1,2 , Cristiane KRUG3, Marcio L. OLIVEIRA1 1 Instituto Nacional de Pesquisas da Amazônia - INPA, Coordenação de Biodiversidade - COBIO, Avenida André Araújo 2936, Petrópolis, CEP 69067-375 Manaus, Amazonas, Brasil 2 Instituto Nacional da Mata Atlântica – INMA, Avenida José Ruschi 4, Santa Teresa, CEP 29650-000, Espírito Santo, Brasil 3 Embrapa Amazônia Ocidental, Rodovia AM-010, Km 29, Manaus, Brasil * Corresponding author: [email protected]; https://orcid.org/0000-0001-9079-9570 https://orcid.org/0000-0003-4574-8111 ABSTRACT We surveyed parasitoid wasps (Hymenoptera) in two guarana plantations in the central Brazilian Amazon (one conventionally, and one organically managed), as well as in adjacent forest and edge areas between crop and forest. We evaluated differences between management systems in parasitoid diversity and abundance, and assessed the importance of the surrounding matrix as a source of parasitoid wasps for guarana cultivation. Parasitoid wasp richness, abundance and taxonomic composition (at family level) were compared between plantations, and among habitats within plantations. Wasps were sampled using Malaise and Moericke traps. A total of 25,951 parasitoid wasps (10,828 in the conventional, and 15,123 in the organic crop area) were collected, and were distributed in 11 superfamilies and 38 families. In the conventional management area, the greatest abundance and richness of parasitoids were recorded in the adjacent forest, while, in the organic management area, the greatest abundance and richness were recorded in the crop-forest edge. -
Ichneumonidae (Hymenoptera) As Biological Control Agents of Pests
Ichneumonidae (Hymenoptera) As Biological Control Agents Of Pests A Bibliography Hassan Ghahari Department of Entomology, Islamic Azad University, Science & Research Campus, P. O. Box 14515/775, Tehran – Iran; [email protected] Preface The Ichneumonidae is one of the most species rich families of all organisms with an estimated 60000 species in the world (Townes, 1969). Even so, many authorities regard this figure as an underestimate! (Gauld, 1991). An estimated 12100 species of Ichneumonidae occur in the Afrotropical region (Africa south of the Sahara and including Madagascar) (Townes & Townes, 1973), of which only 1927 have been described (Yu, 1998). This means that roughly 16% of the afrotropical ichneumonids are known to science! These species comprise 338 genera. The family Ichneumonidae is currently split into 37 subfamilies (including, Acaenitinae; Adelognathinae; Agriotypinae; Alomyinae; Anomaloninae; Banchinae; Brachycyrtinae; Campopleginae; Collyrinae; Cremastinae; Cryptinae; Ctenopelmatinae; 1 Diplazontinae; Eucerotinae; Ichneumoninae; Labeninae; Lycorininae; Mesochorinae; Metopiinae; Microleptinae; Neorhacodinae; Ophioninae; Orthopelmatinae; Orthocentrinae; Oxytorinae; Paxylomatinae; Phrudinae; Phygadeuontinae; Pimplinae; Rhyssinae; Stilbopinae; Tersilochinae; Tryphoninae; Xoridinae) (Yu, 1998). The Ichneumonidae, along with other groups of parasitic Hymenoptera, are supposedly no more species rich in the tropics than in the Northern Hemisphere temperate regions (Owen & Owen, 1974; Janzen, 1981; Janzen & Pond, 1975), although -
Sampling of Parasitoid Hymenoptera 19 Doi: 10.3897/Jhr.78.54309 RESEARCH ARTICLE
JHR 78: 19–31 (2020) Sampling of parasitoid Hymenoptera 19 doi: 10.3897/jhr.78.54309 RESEARCH ARTICLE http://jhr.pensoft.net Sampling of parasitoid Hymenoptera: influence of the height on the ground Ricardo Chan-Canché1, Horacio Ballina-Gómez1, Jorge Leirana-Alcocer2, Santiago Bordera3, Alejandra González-Moreno1 1 Tecnológico Nacional de México/Campus Conkal, Conkal, Mexico 2 Departamento de ecología, Universidad Autónoma de Yucatán, Merida, Mexico 3 Departamento de Ciencias Ambientales y Recursos Naturales, Uni- versidad de Alicante, Alicante, Alicante, Spain Corresponding author: Alejandra González-Moreno ([email protected]) Academic editor: J. Fernandez-Triana | Received 16 May 2020 | Accepted 24 July 2020 | Published 31 August 2020 http://zoobank.org/B3190DCE-D020-42BD-9346-8FB9CAD33541 Citation: Chan-Canche R, Ballina-Gómez H, Leirana-Alcocer J, Bordera S, González-Moreno A (2020) Sampling of parasitoid Hymenoptera: influence of the height on the ground. Journal of Hymenoptera Research 78: 19–31. https://doi. org/10.3897/jhr.78.54309 Abstract Parasitoid hymenopterans are a highly diverse group of insects; therefore, the choice of an adequate sam- pling method becomes important to achieve a representative species richness of a site. The aim of this work is to evaluate the size and diversity of parasitoids in relation to the height of the Malaise trap placement above the ground of a low deciduous forest from Yucatan, Mexico. Parasitoids were collected from Sep- tember to October 2015, using three Malaise traps at ground level and other three located right above the others, leaving no space between them, at a height of 1.5 m. The collected specimens were identified at family level. -
4 Economic Value of Arthropod Biological Control
©CAB International – for Steven Naranjo 4 Economic Value of Arthropod Biological Control STEVEN E. NARANJO1*, GEORGE B. FRISVOLD2 AND PETER C. ELLSWORTH3 1USDA-ARS, Arid-Land Agricultural Research Center, Maricopa, AZ, USA; 2Department of Agricultural and Resource Economics, University of Arizona, Tucson, AZ, USA; 3Department of Entomology, University of Arizona, Maricopa Agricultural Center, Maricopa, AZ, USA Integrated pest management (IPM) is the strategic control are very low, successful programmes have integration of multiple control tactics resulting in the resulted in essentially permanent pest control with amelioration of pest damage that takes into consid- very favourable economic outcomes (Cock et al., eration environmental safety, and the reduction of 2015; Naranjo et al., 2015). risk and favourable economic outcomes for growers A second approach – augmentative biological and society at large. For thousands of years, natural control – involves the initial (inoculation) or enemies of pests have been harnessed for crop pro- repeated (inundation) introduction of native or tection (Simmonds et al., 1976). Maximizing this exotic natural enemies to suppress pest populations. source of natural control is a foundational element Augmentative biological control has been widely in IPM for suppressing the growth of incipient pest and successfully deployed in many parts of the populations (Stern et al., 1959). Biological control world. It is perhaps most well known in protected has been defined as the purposeful use of natural agricultural production, particularly in Europe and enemies, such as predators, parasitoids and patho- in developing regions such as China, India and gens, to regulate another organism’s populations to Latin America (van Lenteren et al., 2017). -
Economics of Biological Control of Cassava Mealybug in Africa
AGRICULTURAL ECONOMICS ELSEVIER Agricultural Economics 24 (200 1) 209-219 www.elsevier.com/locate/agecon Economics of biological control of cassava mealybug in Africa J. Zeddiesa, R.P. Schaaba, P. Neuenschwanderb·*, H.R. Herrenb,l a University of Hohenheim, Institute ofAgricultural Economics (410 B), D-70593 Stuttgart, Germany b International Institute of Tropical Agriculture (l/TA), 08 B.P. 0932, Cotonou, Benin Received 24 December 1997; received in revised form 16 February 2000; accepted 9 March 2000 Abstract Pest populations of the cassava mealybug Phenacoccus manihoti Mat.-Ferr. (Homoptera: Pseudococcidae) were reduced successfully by the biological control agent Apoanagyrus (Epidinocarsis) lopezi De Santis (Hymenoptera: Encyrtidae) throughout most of sub-Saharan Africa. The economics of the project were evaluated based on data from field trials, socio-economic surveys, published results, and financial information provided by the International Institute of Tropical Agriculture (IITA) and the national programmes. Costs and benefits for the biological control of P. manihoti were calculated over 40 years (1974-2013) for 27 African countries, for four different scenarios, taking into account that impact by A. lopezi and speed of the impact differ between ecological zones. A reasonable calculation considering compounded interest resulted in a benefit cost ratio of about 200 when cassava was costed at world market prices, and of about 370-740 when inter-African prices were considered.© 2001 Elsevier Science B.V. All rights reserved. Keywords: Economics of biological control; Phenacoccus manihoti; Apoanagyrus lopezi; Cassava; Africa 1. Introduction decade, the biological control agent had spread to all the major mealybug infestations and had brought the The cassava mealybug Phenacoccus manihoti pest under control in 95% of all the fields (Herren Mat.-Ferr. -
The Mud-Dauber Wasp Is One of the More Commonly Encountered Wasps in Sydney
Yellow jack ground wasp paper wasp (umbrella wasp) Common paper wasps are social insects, who build nests of grey papery material around the home often under eaves, pergolas or in vegetation. Description Polistes humilis or common paper wasps are generally slender with long thin wings. They are 10-15 millimetres long, tan in colour with darker bands and some yellow on the face. Other species of paper wasps are larger or smaller and differently coloured. Paper wasps make nests of grey papery wood fibre material. The nests are cone-shaped, becoming round as more cells are added. Nests are a maximum diameter of 10-12 centimetres, with numerous hexagonal cells underneath, some with white caps. Nests are exposed and suspended by a short stalk under an overhang, often on a pergola, the eaves of a roof or in a shrub or tree. Wasps cluster on the nest or forage in the garden and around buildings. Paper wasps are found across mainland southern Australia including: • southern Queensland • New South Wales • the Australian Capital Territory • Victoria • South Australia • southern Western Australia. Life history Paper wasps are a social wasp consisting of small colonies of 12-20 individuals. Adult wasps feed on nectar and make ‘paper’ nests by mixing saliva and wood fibres. Nests are a nursery where larvae are kept one to each cell. The larvae are fed on chewed-up caterpillars caught by the adults. The cells are then capped and the larvae pupate. Most paper wasps die in autumn or winter, while some hibernate to start new nests next season. -
As a Parasitoid of Agrilus Planipennis Fairmaire
PROC. ENTOMOL. SOC. WASH. 112(2), 2010, pp. 246–257 LELUTHIA ASTIGMA (ASHMEAD) (HYMENOPTERA: BRACONIDAE: DORYCTINAE) AS A PARASITOID OF AGRILUS PLANIPENNIS FAIRMAIRE (COLEOPTERA: BUPRESTIDAE: AGRILINAE), WITH AN ASSESSMENT OF HOST ASSOCIATIONS FOR NEARCTIC SPECIES OF LELUTHIA CAMERON ROBERT R. KULA,KATHLEEN S. KNIGHT,JOANNE REBBECK, LEAH S. BAUER,DAVID L. CAPPAERT, AND KAMAL J. K. GANDHI (RRK) Systematic Entomology Laboratory, Plant Sciences Institute, Agricul- tural Research Service, U.S. Department of Agriculture, c/o National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, MRC 168, Washington, DC 20013-7012, U.S.A. (e-mail: [email protected]); (KSK, JR) U.S. Forest Service Northern Research Station, U.S. Department of Agriculture, 359 Main Road, Delaware, OH 43015, U.S.A.; (LSB) U.S. Forest Service Northern Research Station, U.S. Department of Agriculture, Michigan State University, 1407 S. Harrison Road, East Lansing, MI 48823, U.S.A.; (DLC) Department of Entomology, Michigan State University, East Lansing, MI 48824, U.S.A.; (LSB) U.S. Forest Service Northern Research Station, U.S. Department of Agriculture, Michigan State University, 1407 S. Harrison Road, East Lansing, MI 48823, U.S.A.; (KJKG) Daniel B. Warnell School of Forestry and Natural Resources, The University of Georgia, 180 E Green St., Athens, GA 30602, U.S.A. Abstract.—Published host associations are assessed for Leluthia astigma (Ashmead), Leluthia floridensis Marsh, and Leluthia mexicana Cameron, the three known species of Leluthia Cameron in the Nearctic Region. Leluthia astigma is reported as a parasitoid of Agrilus planipennis Fairmaire, emerald ash borer (EAB), infesting Fraxinus americana L., white ash, in Delaware County, Ohio.