Which Types of Landscape/Habitat Management Are Effective at Providing Natural Pest Control ?
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ARTHROPOD COMMUNITIES and PASSERINE DIET: EFFECTS of SHRUB EXPANSION in WESTERN ALASKA by Molly Tankersley Mcdermott, B.A./B.S
Arthropod communities and passerine diet: effects of shrub expansion in Western Alaska Item Type Thesis Authors McDermott, Molly Tankersley Download date 26/09/2021 06:13:39 Link to Item http://hdl.handle.net/11122/7893 ARTHROPOD COMMUNITIES AND PASSERINE DIET: EFFECTS OF SHRUB EXPANSION IN WESTERN ALASKA By Molly Tankersley McDermott, B.A./B.S. A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Biological Sciences University of Alaska Fairbanks August 2017 APPROVED: Pat Doak, Committee Chair Greg Breed, Committee Member Colleen Handel, Committee Member Christa Mulder, Committee Member Kris Hundertmark, Chair Department o f Biology and Wildlife Paul Layer, Dean College o f Natural Science and Mathematics Michael Castellini, Dean of the Graduate School ABSTRACT Across the Arctic, taller woody shrubs, particularly willow (Salix spp.), birch (Betula spp.), and alder (Alnus spp.), have been expanding rapidly onto tundra. Changes in vegetation structure can alter the physical habitat structure, thermal environment, and food available to arthropods, which play an important role in the structure and functioning of Arctic ecosystems. Not only do they provide key ecosystem services such as pollination and nutrient cycling, they are an essential food source for migratory birds. In this study I examined the relationships between the abundance, diversity, and community composition of arthropods and the height and cover of several shrub species across a tundra-shrub gradient in northwestern Alaska. To characterize nestling diet of common passerines that occupy this gradient, I used next-generation sequencing of fecal matter. Willow cover was strongly and consistently associated with abundance and biomass of arthropods and significant shifts in arthropod community composition and diversity. -
ELIZABETH LOCKARD SKILLEN Diversity of Parasitic Hymenoptera
ELIZABETH LOCKARD SKILLEN Diversity of Parasitic Hymenoptera (Ichneumonidae: Campopleginae and Ichneumoninae) in Great Smoky Mountains National Park and Eastern North American Forests (Under the direction of JOHN PICKERING) I examined species richness and composition of Campopleginae and Ichneumoninae (Hymenoptera: Ichneumonidae) parasitoids in cut and uncut forests and before and after fire in Great Smoky Mountains National Park, Tennessee (GSMNP). I also compared alpha and beta diversity along a latitudinal gradient in Eastern North America with sites in Ontario, Maryland, Georgia, and Florida. Between 1997- 2000, I ran insect Malaise traps at 6 sites in two habitats in GSMNP. Sites include 2 old-growth mesic coves (Porters Creek and Ramsay Cascades), 2 second-growth mesic coves (Meigs Post Prong and Fish Camp Prong) and 2 xeric ridges (Lynn Hollow East and West) in GSMNP. I identified 307 species (9,716 individuals): 165 campoplegine species (3,273 individuals) and a minimum of 142 ichneumonine species (6,443 individuals) from 6 sites in GSMNP. The results show the importance of habitat differences when examining ichneumonid species richness at landscape scales. I report higher richness for both subfamilies combined in the xeric ridge sites (Lynn Hollow West (114) and Lynn Hollow East (112)) than previously reported peaks at mid-latitudes, in Maryland (103), and lower than Maryland for the two cove sites (Porters Creek, 90 and Ramsay Cascades, 88). These subfamilies appear to have largely recovered 70+ years after clear-cutting, yet Campopleginae may be more susceptible to logging disturbance. Campopleginae had higher species richness in old-growth coves and a 66% overlap in species composition between previously cut and uncut coves. -
15 Foottit:15 Foottit
REDIA, XCII, 2009: 87-91 ROBERT G. FOOTTIT (*) - H. ERIC L. MAW (*) - KEITH S. PIKE (**) DNA BARCODES TO EXPLORE DIVERSITY IN APHIDS (HEMIPTERA APHIDIDAE AND ADELGIDAE) (*) Canadian National Collection of Insects, National Environmental Health Program, Agriculture and Agri-Food Canada, K.W. Neatby Building, 960 Carling Avenue, Ottawa, Ontario K1A 0C6, Canada;[email protected] (**) Washington State University, Irrigated Agriculture Research and Extension Center, 24106 N. Bunn Road, Prosser, WA 99350, U.S.A Foottit R.G., Maw H.E.L., Pike K.S. – DNA barcodes to explore diversity in aphids (Hemiptera Aphididae and Adelgidae). A tendency towards loss of taxonomically useful characters, and morphological plasticity due to host and environmental factors, complicates the identification of aphid species and the analysis of relationships. The presence of different morphological forms of a single species on different hosts and at different times of the year makes it difficult to consistently associate routinely collected field samples with particular species definitions. DNA barcoding has been proposed as a standardized approach to the characterization of life forms. We have tested the effectiveness of the standard 658-bp barcode fragment from the 5’ end of the mitochondrial cytochrome c oxidase 1 gene (COI) to differentiate among species of aphids and adelgids. Results are presented for a preliminary study on the application of DNA barcoding in which approximately 3600 specimens representing 568 species and 169 genera of the major subfamilies of aphids and the adelgids have been sequenced. Examples are provided where DNA barcoding has been used as a tool in recognizing the existence of cryptic new taxa, linking life stages on different hosts of adelgids, and as an aid in the delineation of species boundaries. -
Pdf 696.18 K
Egypt. Acad. J. Biolog. Sci., 13(3):1-13 (2020) Egyptian Academic Journal of Biological Sciences A. Entomology ISSN 1687- 8809 http://eajbsa.journals.ekb.eg/ The Mymaridae of Egypt (Chalcidoidea: Hymenoptera) Al-Azab, S. A. Plant Protection Research Institute, ARC, Egypt. Email: [email protected] ______________________________________________________________ ARTICLE INFO ABSTRACT Article History Diagnostic characters of the family Mymaridae, together with diagnosis Received:15/5/2020 and keys to the Egyptian genera of the family-based upon the external Accepted:2/7/2020 morphological characters of the adult female and male are presented with ---------------------- illustrations to facilitate their recognition. Synonyms, taxonomic notes, hosts, Keywords: and habitat of the genera together with their representative species in Egypt Hymenoptera, are also provided to give general picture and high light on the occurrence, Chalcidoidea, diversity, and distribution of the mymarids in Egypt. The study based on the Mymaridae, materials kept in the main reference insect collections in Egypt, and the Taxonomy, available literature. Egypt. INTRODUCTION The Mymaridae (fairy wasps) are a family of chalcid wasps found in temperate and tropical regions throughout the world. It includes the most primitive members of the chalcid wasp and contains around 100 genera with about 1400 species (Noyes, 2005). Fairyflies are very tiny insects and include the world's smallest known insects. They generally range from 0.5 to 1.0 mm long. Adult mymarids are rather fragile, the body generally being slender and the wings narrow with an elongate marginal fringe. Their delicate bodies and their hair-fringed wings have earned them their common name. Very little is known of the life histories of fairyflies, as only a few species have been observed extensively. -
Bugila Phd Thesis Document Final
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by UTL Repository Host-parasitoid relationships of Anagyrus sp. near pseudococci (Girault), (Hymenoptera, Encyrtidae), as a basis to improve biological control of pest mealybugs (Hemiptera, Pseudococcidae) TESE APRESENTADA PARA OBTENÇÃO DO GRAU DE DOUTOR EM ENGENHARIA AGRONÓMICA Abdalbaset Abusalah Ali Bugila Orientador: Professor Doutor José Carlos Franco Santos Silva Co-orientador: Professora Doutora Manuela Rodrigues Branco Simões JÚRI: Presidente : Reitor da Universidade de Lisboa Vogais: Doutora Laura Monteiro Torres Professora Catedrática, Escola de Ciências Agrárias e Veterinárias da Universidade de Trás-os-Montes e Alto Douro Doutor António Maria Marques Mexia Professor Catedrático, Instituto Superior de Agronomia da Universidade de Lisboa Doutor David João Horta Lopes Professor Auxiliar com agregação, Universidade dos Açores; Doutor José Carlos Franco Santos Silva Professor Auxiliar, Instituto Superior de Agronomia da Universidade de Lisboa Doutora Elisabete Tavares Lacerda de Figueiredo Oliveira Professora Auxiliar, Instituto Superior de Agronomia da Universidade de Lisboa. LISBOA 2014 Index Abstract vii ....................................................................................................................... Resumo viii ………………………………………………………………………..….…. 1. Introduction 1 ………………………………………………………………….….. 1.1. State of the art 2 …………………………………………………………….…. 1.2. Objectives 4 …………………………………………………………………..... 1.3. References 5 ……………………………………………………………….….. -
Data Sheets on Quarantine Pests
Prepared by CABI and EPPO for the EU under Contract 90/399003 Data Sheets on Quarantine Pests Aonidiella citrina IDENTITY Name: Aonidiella citrina (Coquillett) Synonyms: Aspidiotus citrinus Coquillett Chrysomphalus aurantii citrinus (Coquillett) Taxonomic position: Insecta: Hemiptera: Homoptera: Diaspididae Common names: Yellow scale (English) Cochenille jaune (French) Escama amarilla de los cítricos (Spanish) Notes on taxonomy and nomenclature: The original description by Coquillett is inadequate and simply refers to 'the yellow scale' on orange (Nel, 1933). A. citrina is morphologically very similar to the Californian red scale, Aonidiella aurantii (Maskell), and was considered to be a variety until Nel (1933) raised it to specific level based on a comparative study of their ecology, biology and morphology. Bayer computer code: AONDCI EU Annex designation: II/A1 HOSTS A. citrina is polyphagous attacking plant species belonging to more than 50 genera in 32 families. The main hosts of economic importance are Citrus spp., especially oranges (C. sinensis), but the insect is also recorded incidentally on a wide range of ornamentals and some fruit crops including Acacia, bananas (Musa paradisiaca), Camellia including tea (C. sinensis), Clematis, Cucurbitaceae, Eucalyptus, Euonymus, guavas (Psidium guajava), Hedera helix, Jasminum, Ficus, Ligustrum, Magnolia, mangoes (Mangifera indica), Myrica, olives (Olea europea), peaches (Prunus persica), poplars (Populus), Rosa, Schefflera actinophylla, Strelitzia reginae, Viburnum and Yucca. The main potential hosts in the EPPO region are Citrus spp. growing in the southern part of the region, around the Mediterranean. GEOGRAPHICAL DISTRIBUTION A. citrina originated in Asia and has spread to various tropical and subtropical regions throughout the world. The precise distribution of A. -
Insecticides - Development of Safer and More Effective Technologies
INSECTICIDES - DEVELOPMENT OF SAFER AND MORE EFFECTIVE TECHNOLOGIES Edited by Stanislav Trdan Insecticides - Development of Safer and More Effective Technologies http://dx.doi.org/10.5772/3356 Edited by Stanislav Trdan Contributors Mahdi Banaee, Philip Koehler, Alexa Alexander, Francisco Sánchez-Bayo, Juliana Cristina Dos Santos, Ronald Zanetti Bonetti Filho, Denilson Ferrreira De Oliveira, Giovanna Gajo, Dejane Santos Alves, Stuart Reitz, Yulin Gao, Zhongren Lei, Christopher Fettig, Donald Grosman, A. Steven Munson, Nabil El-Wakeil, Nawal Gaafar, Ahmed Ahmed Sallam, Christa Volkmar, Elias Papadopoulos, Mauro Prato, Giuliana Giribaldi, Manuela Polimeni, Žiga Laznik, Stanislav Trdan, Shehata E. M. Shalaby, Gehan Abdou, Andreia Almeida, Francisco Amaral Villela, João Carlos Nunes, Geri Eduardo Meneghello, Adilson Jauer, Moacir Rossi Forim, Bruno Perlatti, Patrícia Luísa Bergo, Maria Fátima Da Silva, João Fernandes, Christian Nansen, Solange Maria De França, Mariana Breda, César Badji, José Vargas Oliveira, Gleberson Guillen Piccinin, Alan Augusto Donel, Alessandro Braccini, Gabriel Loli Bazo, Keila Regina Hossa Regina Hossa, Fernanda Brunetta Godinho Brunetta Godinho, Lilian Gomes De Moraes Dan, Maria Lourdes Aldana Madrid, Maria Isabel Silveira, Fabiola-Gabriela Zuno-Floriano, Guillermo Rodríguez-Olibarría, Patrick Kareru, Zachaeus Kipkorir Rotich, Esther Wamaitha Maina, Taema Imo Published by InTech Janeza Trdine 9, 51000 Rijeka, Croatia Copyright © 2013 InTech All chapters are Open Access distributed under the Creative Commons Attribution 3.0 license, which allows users to download, copy and build upon published articles even for commercial purposes, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications. After this work has been published by InTech, authors have the right to republish it, in whole or part, in any publication of which they are the author, and to make other personal use of the work. -
(Aphelinidae, Hymenoptera) Parasitizing Myzus Persicae (Sulzer) Under Protected Cultivation
Journal of Biological Control, 26 (3): 283–284, 2012 Research Note Occurrence of Aphelinus asychis Walker (Aphelinidae, Hymenoptera) parasitizing Myzus persicae (Sulzer) under protected cultivation GAVKARE OMKAR* and KUMAR SURJEET Department of Entomology, CSK HPKV, Palampur 176 062, Himachal Pradesh, India * Corresponding author: E-mail: [email protected] ABSTRACT: Aphelinus asychis Walker (Aphelinidae: Hymenoptera), a solitary endoparasitoid was recorded from Myzus persicae (Sulzer) infesting bell pepper Capsicum annuum L. under protected cultivation in India during December 2011. The per cent parasitisation ranged from 35 to 40% of population of M. persicae. KEY WORDS: Aphelinus asychis, Myzus persicae, endoparasitoid, protected cultivation (Article chronicle: Received: 31-5-2012 Revised: 23-8-2012 Accepted: 10-9-2012) Aphelinus asychis Walker (Hymenoptera: Aphelinidae) morphological studies, the parasitoids were mounted in is a solitary endoparasitoid of aphids and native to Old DPX and permanent slides were prepared which were World (Europe, Asia and Africa). It was introduced into observed under stereozoom microscope (SMZ 16, the United States from Asia, Europe and Africa for classical Olympus, Japan) equipped with a photo-micrograph biological control of the Russian wheat aphid, Diuraphis camera. Morphometric observations of the parasitoid noxia Mordivilko and the species is cosmopolitan now were also carried out using an ocular micrometer calibrated as a result of previous introductions (Hayat 1998; Elliott with a stage micrometer. The adult parasitoid was a et al., 1999). This species parasitizes different hosts at tiny black wasp with an average length and breadth of different geographical locations. At least 42 species of 1.50 mm and 0.54 mm respectively. -
Monitoring of Pear Psylla for Pest Management Decisions and Research
Integrated Pest Management Reviews 4: 1–20, 1999. © 1999 Kluwer Academic Publishers. Printed in the Netherlands. Monitoring of pear psylla for pest management decisions and research David R. Horton USDA-ARS, 5230 Konnowac Pass Rd., Wapato, WA 98951 U.S.A. (Tel.: (509) 454-5639; Fax: 509-454-5646) Received 6 May 1998; accepted 3 November 1998 Abstract Pear psylla, Cacopsylla pyricola (Foerster) (Homoptera: Psyllidae), is one of the key insect pests in North American pear production. In some growing areas, more than 50% of dollars spent to control arthropod pests in commercial pear are directed specifically at controlling this species. Control measures require accurate and timely information about dispersal, onset of egg-laying in spring, densities in the orchard, and age composition of the population. To meet these ends, a number of sampling methods have been developed to monitor pear psylla, the most common being (for pest management purposes) visual inspection of spurs and foliage for nymphs and eggs, and use of beat trays to monitor adults. Action thresholds have been developed for counts obtained with either method. However, threshold estimates are fairly narrowly defined, referring to a somewhat limited group of pear cultivars, type of injury to be prevented, and pest management program being used. Further refinement has been difficult because of an incomplete understanding of psylla’s spatial distribution, seasonal changes in spatial distribution, and unknown or seasonally changing action thresholds. Beat trays and visual inspection of foliage have also been used to monitor pear psylla in various types of research projects, including studies of dispersal and biological control. -
Parasitism of the Soybean Aphid, Aphis Glycines by Binodoxys Communis: the Role of Aphid Defensive Behaviour and Parasitoid Reproductive Performance
Bulletin of Entomological Research (2008) 98, 361–370 doi:10.1017/S000748530800566X Ó 2008 Cambridge University Press Printed in the United Kingdom First published online 25 February 2008 Parasitism of the soybean aphid, Aphis glycines by Binodoxys communis: the role of aphid defensive behaviour and parasitoid reproductive performance K.A.G. Wyckhuys1 *, L. Stone3, N. Desneux2, K.A. Hoelmer4, K.R. Hopper4 and G.E. Heimpel2 1Horticulture Research Center, Universidad Jorge Tadeo Lozano, Chia (Cundinamarca), Colombia: 2Department of Entomology, University of Minnesota, St. Paul, USA: 3Saint Olaf College, Northfield, Minnesota, USA: 4Beneficial Insect Introductions Research Unit, USDA-ARS, Newark, Delaware, USA Abstract The Asian parasitoid, Binodoxys communis (Gahan) (Hymenoptera: Braconidae), is a candidate for release against the exotic soybean aphid, Aphis glycines Matsumura (Hemiptera: Aphididae), in North America. In this study, we examined preferences by B. communis for the different developmental stages of A. glycines and investigated consequences of these preferences for parasitoid fitness. We also determined to what extent aphid defensive behaviours mediate such preferences. We found that B. communis readily attacks and successfully develops in the different A. glycines developmental stages. Binodoxys communis development time gradually increased with aphid developmental stage, and wasps took longest to develop in alates. An average (+SE) of 54.01+0.08% of parasitized A. glycines alatoid nymphs transformed into winged adult aphids prior to mummification. No-choice assays showed a higher proportion of successful attacks for immature apterous A. glycines nymphs compared to adults and alatoid nymphs. Also, choice trials indicated avoidance and lower attack and oviposition of adults and alatoid nymphs. -
Hymenoptera Parasitoid Complex of Prays Oleae (Bernard) (Lepidoptera: Praydidae) in Portugal
Turkish Journal of Zoology Turk J Zool (2017) 41: 502-512 http://journals.tubitak.gov.tr/zoology/ © TÜBİTAK Research Article doi:10.3906/zoo-1603-50 Hymenoptera parasitoid complex of Prays oleae (Bernard) (Lepidoptera: Praydidae) in Portugal 1, 1 2 3 4 1 Anabela NAVE *, Fátima GONÇALVES , Rita TEIXEIRA , Cristina AMARO COSTA , Mercedes CAMPOS , Laura TORRES 1 Centre for the Research and Technology of Agro-Environmental and Biological Sciences, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal 2 Agrarian and Forestry Systems and Plant Health, National Institute of Agricultural and Veterinary Research, Oeiras, Portugal 3 Department of Ecology and Sustainable Agriculture, Agrarian School, Polytechnic Institute of Viseu, Viseu, Portugal 4 Department of Environmental Protection, Experimental Station Zaidín, Granada, Spain Received: 23.03.2016 Accepted/Published Online: 29.11.2016 Final Version: 23.05.2017 Abstract: The olive moth, Prays oleae (Bernard) (Lepidoptera: Praydidae), is one of the most important pests of olive trees throughout the Mediterranean region, the Black Sea, the Middle East, and the Canary Islands. Thus, it is particularly important to develop alternative strategies to control this pest. Over a 4-year period, a survey was done in order to acquire knowledge about the complex of parasitoids associated with this pest. Leaves, flowers, and fruit infested with larvae and pupae of P. oleae were collected from olive groves, conditioned in vials, and kept under laboratory conditions until the emergence of P. ol e ae adults or parasitoids. The abundance and richness of parasitoids as well as the rate of parasitism was estimated. Hymenoptera parasitoids were found to be responsible for 43% of the mean mortality of the sampled individuals. -
Aphid Species (Hemiptera: Aphididae) Infesting Medicinal and Aromatic Plants in the Poonch Division of Azad Jammu and Kashmir, Pakistan
Amin et al., The Journal of Animal & Plant Sciences, 27(4): 2017, Page:The J.1377 Anim.-1385 Plant Sci. 27(4):2017 ISSN: 1018-7081 APHID SPECIES (HEMIPTERA: APHIDIDAE) INFESTING MEDICINAL AND AROMATIC PLANTS IN THE POONCH DIVISION OF AZAD JAMMU AND KASHMIR, PAKISTAN M. Amin1, K. Mahmood1 and I. Bodlah 2 1 Faculty of Agriculture, Department of Entomology, University of Poonch, 12350 Rawalakot, Azad Jammu and Kashmir, Pakistan 2Department of Entomology, PMAS-Arid Agriculture University, 46000 Rawalpindi, Pakistan Corresponding Author Email: [email protected] ABSTRACT This study conducted during 2015-2016 presents first systematic account of the aphids infesting therapeutic herbs used to cure human and veterinary ailments in the Poonch Division of Azad Jammu and Kashmir, Pakistan. In total 20 aphid species, representing 12 genera, were found infesting 35 medicinal and aromatic plant species under 31 genera encompassing 19 families. Aphis gossypii with 17 host plant species was the most polyphagous species followed by Myzus persicae and Aphis fabae that infested 15 and 12 host plant species respectively. Twenty-two host plant species had multiple aphid species infestation. Sonchus asper was infested by eight aphid species and was followed by Tagetes minuta, Galinosoga perviflora and Chenopodium album that were infested by 7, 6 and 5 aphid species respectively. Asteraceae with 11 host plant species under 10 genera, carrying 13 aphid species under 8 genera was the most aphid- prone plant family. A preliminary systematic checklist of studied aphids and list of host plant species are provided. Key words: Aphids, Medicinal/Aromatic plants, checklist, Poonch, Kashmir, Pakistan.