Aphids in Alfalfa Fact Sheet No
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Geostatistical Analysis of Spatial Distribution of Therioaphis Maculata (Hemiptera: Aphididae) and Coccinellid Lady Beetles (Coleoptera: Coccinellidae)
J. Crop Prot. 2019, 8 (1): 103-115______________________________________________________ Research Article Geostatistical analysis of spatial distribution of Therioaphis maculata (Hemiptera: Aphididae) and coccinellid lady beetles (Coleoptera: Coccinellidae) Hakimeh Shayestehmehr and Roghaiyeh Karimzadeh* Department of Plant Protection, Faculty of Agriculture, University of Tabriz, Tabriz, Iran. Abstract: Understanding the spatial dynamics of insect distributions provides useful information about their ecological requirements and can also be used in site-specific pest management programs. Interactions between prey and predator are spatially and temporally dynamic and can be affected by several factors. In this study, geostatistics was used to characterize the spatial variability of spotted alfalfa aphid, Therioaphis maculata Buckton and coccinellid lady beetles in alfalfa fields. Global positioning and geographic information systems were used for spatial sampling and mapping the distribution pattern of these insects. This study was conducted in three alfalfa fields with areas of 7.3, 3.1 and 0.5 ha and two growing seasons, 2013 and 2014. The 0.5 ha field was divided into 10 × 10m grids and 3.1 and 7.3 ha fields were divided into 30 × 30m grids. Weekly sampling began when height of alfalfa plants reached about 15cm and was continued until the cuttings of alfalfa hay. For sampling, 40 and 10 stems were chosen randomly in 30 × 30m and 10 × 10m grids, respectively and shaken into a white pan three times. Aphids and coccinellids fallen in the pan were counted and recorded. Semivariance analysis indicated that distribution of T. maculata and coccinellids was aggregated in the fields. Comparison of the distribution maps of aphid and lady beetles indicated that there was an overlap between the maps, but they did not coincide completely. -
Jordan Beans RA RMO Dir
Importation of Fresh Beans (Phaseolus vulgaris L.), Shelled or in Pods, from Jordan into the Continental United States A Qualitative, Pathway-Initiated Risk Assessment February 14, 2011 Version 2 Agency Contact: Plant Epidemiology and Risk Analysis Laboratory Center for Plant Health Science and Technology United States Department of Agriculture Animal and Plant Health Inspection Service Plant Protection and Quarantine 1730 Varsity Drive, Suite 300 Raleigh, NC 27606 Pest Risk Assessment for Beans from Jordan Executive Summary In this risk assessment we examined the risks associated with the importation of fresh beans (Phaseolus vulgaris L.), in pods (French, green, snap, and string beans) or shelled, from the Kingdom of Jordan into the continental United States. We developed a list of pests associated with beans (in any country) that occur in Jordan on any host based on scientific literature, previous commodity risk assessments, records of intercepted pests at ports-of-entry, and information from experts on bean production. This is a qualitative risk assessment, as we express estimates of risk in descriptive terms (High, Medium, and Low) rather than numerically in probabilities or frequencies. We identified seven quarantine pests likely to follow the pathway of introduction. We estimated Consequences of Introduction by assessing five elements that reflect the biology and ecology of the pests: climate-host interaction, host range, dispersal potential, economic impact, and environmental impact. We estimated Likelihood of Introduction values by considering both the quantity of the commodity imported annually and the potential for pest introduction and establishment. We summed the Consequences of Introduction and Likelihood of Introduction values to estimate overall Pest Risk Potentials, which describe risk in the absence of mitigation. -
A Contribution to the Aphid Fauna of Greece
Bulletin of Insectology 60 (1): 31-38, 2007 ISSN 1721-8861 A contribution to the aphid fauna of Greece 1,5 2 1,6 3 John A. TSITSIPIS , Nikos I. KATIS , John T. MARGARITOPOULOS , Dionyssios P. LYKOURESSIS , 4 1,7 1 3 Apostolos D. AVGELIS , Ioanna GARGALIANOU , Kostas D. ZARPAS , Dionyssios Ch. PERDIKIS , 2 Aristides PAPAPANAYOTOU 1Laboratory of Entomology and Agricultural Zoology, Department of Agriculture Crop Production and Rural Environment, University of Thessaly, Nea Ionia, Magnesia, Greece 2Laboratory of Plant Pathology, Department of Agriculture, Aristotle University of Thessaloniki, Greece 3Laboratory of Agricultural Zoology and Entomology, Agricultural University of Athens, Greece 4Plant Virology Laboratory, Plant Protection Institute of Heraklion, National Agricultural Research Foundation (N.AG.RE.F.), Heraklion, Crete, Greece 5Present address: Amfikleia, Fthiotida, Greece 6Present address: Institute of Technology and Management of Agricultural Ecosystems, Center for Research and Technology, Technology Park of Thessaly, Volos, Magnesia, Greece 7Present address: Department of Biology-Biotechnology, University of Thessaly, Larissa, Greece Abstract In the present study a list of the aphid species recorded in Greece is provided. The list includes records before 1992, which have been published in previous papers, as well as data from an almost ten-year survey using Rothamsted suction traps and Moericke traps. The recorded aphidofauna consisted of 301 species. The family Aphididae is represented by 13 subfamilies and 120 genera (300 species), while only one genus (1 species) belongs to Phylloxeridae. The aphid fauna is dominated by the subfamily Aphidi- nae (57.1 and 68.4 % of the total number of genera and species, respectively), especially the tribe Macrosiphini, and to a lesser extent the subfamily Eriosomatinae (12.6 and 8.3 % of the total number of genera and species, respectively). -
Iáe Comparative Host Plant Range Studies Ofthebluealfaifa
STMSÍ^- ^ iáe Comparative Host Science and Education Administration Plant Range Studies Technical Bulletin oftheBlueAlfaifa Number 1 639 Aphiid, Acyrthosiphon Kon do/Sh in ji, and the Pea Aphid, Acyrthosiphon Pisum (l-iarris) (IHomoptera: Aphid idae) O :"-.;::>-"' C'" p _ ' ./ -• - -. -.^^ ■ ■ ■ ■ 'Zl'-'- CO ^::!:' ^. ^:"^"^ >^. 1 - «# V1--; '"^I I-*"' Í""' C30 '-' C3 ci :x: :'— -xj- -- rr- ^ T> r-^- C".' 1- 03—' O '-■:: —<' C-_- ;z: ë^GO Acknowledgments Contents Page The authors wish to thank Robert O. Kuehl and the staff Introduction -| of the Center for Quantitative Studies, University of Materials and methods -| Arizona, for their assistance in statistical analysis of Greenhouse studies -| these data. We are also grateful to S. M. Dietz, G. L Jordan, A. M. Davis, and W. H. Skrdia for providing seed Field studies 2 used in these studies. Statistical analyses 3 Resultsanddiscussion 3 Abstract Greenhouse studies 3 Field studies 5 Ellsbury, Michael M., and Nielsen, Mervin W. 1981. Classification of hosts studied in field and Comparative Host Plant Range Studies of the Blue greenhouse experiments 5 Alfalfa Aphid, Acyrthosiphon kondoi Shinji, and the Pea Conclusions Q Aphid, Acyrthosiphon pisum (Harris) (Homoptera: Literature cited 5 Aphididae). U.S. Departnnent of Agriculture, Technical Appendix 7 Bulletin No. 1639, 14 p. Host plant ranges of the blue alfalfa aphid (BAA), Acyrthosiphon kondoi Shinji, and the pea aphid (PA), Acyrthosiphon pisum (Harris), were investigated on leguminous plant species. Fecundities of BAA and PA were determined on 84 plant species from the genera Astragalus, Coronilla, Lathyrus, Lens, Lotus, Lupinus, Medicago, Melilotus, Ononis, Phaseolus, Pisum, Trifolium, Vicia, and Vigna in greenhouse studies. Both aphids displayed a broad reproductive host range extending to species in all genera tested except Phaseolus. -
Infection Cycle of Watermelon Mosaic Virus
Infection Cycle of Watermelon Mosaic Virus By TAKASHI YAMAMOTO* Agronomy Division, Shikoku National Agricultural Experiment Station (Senyucho, Zentsuji, Kagawa, 765 Japan) Among the viruses occurring in cucurbits transmission. As to other vectors, many of in Japan, the most prevalent ones are water them showed low parasitism to cucurbits and melon mosaic virus (WMV) and cucumber low ability of transmitting WMV, so that their mosaic virus (CMV) . Of them, WMV occurs role for the spread of WMV in the field was mainly in the summer season in the Kanto not clear. A survey conducted in fields of region and westward. The WMV diseases in cucurbits in 1981 spring to know the kinds of cucurbits cause not only systemic symptoms aphids which fly to the cucurbits at the initial such as mosaic, dwarf, etc. but also fruit mal incidence of WMV showed that more than a formation, thus giving severe damage to crops. half of the aphid species sampled were vector In addition, the control of WMV is quite dif species (Table 2). The initial incidence of ficult as the virus is transmitted by aphids WMV occurs usually in the period from mid and that carried by plant sap is also infectious. May to early-June at the survey site (west Thus, WMV is one of the greatest obstacles part of Kagawa Prefecture), and this period to the production of cucurbits. coincides with the period of abundant appear The infection cycle of the WMV, including ance of aphids. In this period, vector species the routes of transmission of the virus by less parasitic to cucurbits also flew in plenty aphids, which is the most important in con to cucurbits. -
Aphids (Hemiptera, Aphididae)
A peer-reviewed open-access journal BioRisk 4(1): 435–474 (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2 435 doi: 10.3897/biorisk.4.57 RESEARCH ARTICLE BioRisk www.pensoftonline.net/biorisk Aphids (Hemiptera, Aphididae) Chapter 9.2 Armelle Cœur d’acier1, Nicolas Pérez Hidalgo2, Olivera Petrović-Obradović3 1 INRA, UMR CBGP (INRA / IRD / Cirad / Montpellier SupAgro), Campus International de Baillarguet, CS 30016, F-34988 Montferrier-sur-Lez, France 2 Universidad de León, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, 24071 – León, Spain 3 University of Belgrade, Faculty of Agriculture, Nemanjina 6, SER-11000, Belgrade, Serbia Corresponding authors: Armelle Cœur d’acier ([email protected]), Nicolas Pérez Hidalgo (nperh@unile- on.es), Olivera Petrović-Obradović ([email protected]) Academic editor: David Roy | Received 1 March 2010 | Accepted 24 May 2010 | Published 6 July 2010 Citation: Cœur d’acier A (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2. In: Roques A et al. (Eds) Alien terrestrial arthropods of Europe. BioRisk 4(1): 435–474. doi: 10.3897/biorisk.4.57 Abstract Our study aimed at providing a comprehensive list of Aphididae alien to Europe. A total of 98 species originating from other continents have established so far in Europe, to which we add 4 cosmopolitan spe- cies of uncertain origin (cryptogenic). Th e 102 alien species of Aphididae established in Europe belong to 12 diff erent subfamilies, fi ve of them contributing by more than 5 species to the alien fauna. Most alien aphids originate from temperate regions of the world. Th ere was no signifi cant variation in the geographic origin of the alien aphids over time. -
Comparative Host Plant Range Studies of the Blue Alfalfa Aphid, Acyrthosiphon Kondoi Shinji, and the Pea Aphid, Acyrthosiphon Pisum (Harris) (Homoptera: Aphididae)
t ... !' -, ~12,8 ~~2.5 ~W '1 2,5 W ~ 1.0 W w I~ 2.2 wlji w 11111 w 2.2 &.:: I~ &.::~ a:. a:. ~ ~ ::t ~ ... M 1.1 ..".. /1.1 .."... ..M I 4 '''''1.25/1'''1.4 111111.6 1111,1.25"",1. 111111.6 MICROCOPY RESOLUTION TEST CHART MICROCOPY RESOLUTION TEST CHART NATIONAL BUREAU or ST ANDARDS-1963-A NATIONAL BUREAU or :;iANDARDS-1963-A ~~\ United States {~ Department of ~ Agriculture Comparative Host Science and Education Adm in istration Plant Range Studies Technical B:.Jlletln of the Blue Alfalfa Number 1639 Aphid, Acyrthosiphon Kondoi Shinji, and the Pea Aphid, Acyrthosiphon Pisum (Harris) ( Homoptera: Aphididae) Acknowledgments Contents Page The authors wish to thank Robert O. Kuehl and the staff Introduction ___________________________________ 1 of the Center for Quantitative Studies, University of Materials and methods __________________________ 1 Arizona, for their assistance in statistical analysis of Greenhousestudies___________________________ 1 these data. We are also grateful to S. M. Dietz, G. L. Field studies _________________________________ 2 Jordan. A. M. Davis, and W. H. Skrdla for providing seed Statistical analyses ___________________________ 3 used in these studies. Results and discussion __________________________ 3 Greenhouse studies____________ ._______________ 3 Abstract Field studies_________________________________ 5 Ellsbury. Michael M., and Nielson. Mervin W. 1981. Classification of hosts studied in field and Comparative Host Plant Range Studies of the Blue greenhouse experi ments_____________________ 5 Aifalfa Aphid. Acyrthosiphon kondoi Shinji. and the Pea Conclusions ___________________________________ 6 Aphid. Acyrthosiphon pisum (Harris) (Homoptera: Literature cited_________________________________ 6 Aphididae). U.S. Department of Agriculture, Technical Appendix________________________________ ------ 7 Bulletin No. 1639. 14 p. Host plant ranges of the b!~le alfalfa aphid (BAA), Acyrthosiphon kondoi Sh;11ji, and the pea aphid (PA), Acyrthosiphon pisum (Harris), were investigated on leguminous plant species. -
Obligate Bacterial Endosymbionts Limit Thermal Tolerance of Insect Host Species
Obligate bacterial endosymbionts limit thermal tolerance of insect host species Bo Zhanga,b, Sean P. Leonardb, Yiyuan Lib, and Nancy A. Moranb,1 aLaboratory of Predatory Mites, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, 100193 Beijing, People’s Republic of China; and bDepartment of Integrative Biology, University of Texas, Austin, TX 78712 Edited by David L. Denlinger, The Ohio State University, Columbus, OH, and approved October 22, 2019 (received for review September 6, 2019) The thermal tolerance of an organism limits its ecological and acid replacements, including replacements that affect translational geographic ranges and is potentially affected by dependence on machinery itself, leading to decline in protein quality (9). temperature-sensitive symbiotic partners. Aphid species vary widely Aphids and their intracellular bacterial associates Buchnera in heat sensitivity, but almost all aphids are dependent on the aphidicola are a widely studied model of obligate symbiosis. nutrient-provisioning intracellular bacterium Buchnera, which has Buchnera has diversified with aphids through maternal trans- evolved with aphids for 100 million years and which has a reduced mission for >100 million years; their tiny genomes encode only genome potentially limiting heat tolerance. We addressed whether 354–587 proteins (10) but retain genes underlying production of heat sensitivity of Buchnera underlies variation in thermal tolerance amino acids needed for host nutrition (11). Several observations among 5 aphid species. We measured how heat exposure of juve- suggest that Buchnera is heat sensitive. First, Buchnera proteins nile aphids affects later survival, maturation time, and fecundity. At show reduced thermal stability compared to homologous pro- one extreme, heat exposure of Aphis gossypii enhanced fecundity teins of related free-living bacteria (12). -
Aphid Transmission of Potyvirus: the Largest Plant-Infecting RNA Virus Genus
Supplementary Aphid Transmission of Potyvirus: The Largest Plant-Infecting RNA Virus Genus Kiran R. Gadhave 1,2,*,†, Saurabh Gautam 3,†, David A. Rasmussen 2 and Rajagopalbabu Srinivasan 3 1 Department of Plant Pathology and Microbiology, University of California, Riverside, CA 92521, USA 2 Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC 27606, USA; [email protected] 3 Department of Entomology, University of Georgia, 1109 Experiment Street, Griffin, GA 30223, USA; [email protected] * Correspondence: [email protected]. † Authors contributed equally. Received: 13 May 2020; Accepted: 15 July 2020; Published: date Abstract: Potyviruses are the largest group of plant infecting RNA viruses that cause significant losses in a wide range of crops across the globe. The majority of viruses in the genus Potyvirus are transmitted by aphids in a non-persistent, non-circulative manner and have been extensively studied vis-à-vis their structure, taxonomy, evolution, diagnosis, transmission and molecular interactions with hosts. This comprehensive review exclusively discusses potyviruses and their transmission by aphid vectors, specifically in the light of several virus, aphid and plant factors, and how their interplay influences potyviral binding in aphids, aphid behavior and fitness, host plant biochemistry, virus epidemics, and transmission bottlenecks. We present the heatmap of the global distribution of potyvirus species, variation in the potyviral coat protein gene, and top aphid vectors of potyviruses. Lastly, we examine how the fundamental understanding of these multi-partite interactions through multi-omics approaches is already contributing to, and can have future implications for, devising effective and sustainable management strategies against aphid- transmitted potyviruses to global agriculture. -
Eco-Climatic Assessment of the Potential Establishment of Exotic Insects in New Zealand
Eco-climatic assessment of the potential establishment of exotic insects in New Zealand A thesis submitted in partial fulfillment of the requirements for the Degree of Doctor of Philosophy at Lincoln University by Lora Peacock Lincoln University 2005 Contents Abstract of a thesis submitted in partial fulfillment of the requirements for the Degree of PhD Eco-climatic assessment of the potential establishment of exotic insects in New Zealand Lora Peacock To refine our knowledge and to adequately test hypotheses concerning theoretical and applied aspects of invasion biology, successful and unsuccessful invaders should be compared. This study investigated insect establishment patterns by comparing the climatic preferences and biological attributes of two groups of polyphagous insect species that are constantly intercepted at New Zealand's border. One group of species is established in New Zealand (n = 15), the other group comprised species that are not established (n = 21). In the present study the two groups were considered to represent successful and unsuccessful invaders. To provide background for interpretation of results of the comparative analysis, global areas that are climatically analogous to sites in New Zealand were identified by an eco climatic assessment model, CLIMEX, to determine possible sources of insect pest invasion. It was found that south east Australia is one of the regions that are climatically very similar to New Zealand. Furthermore, New Zealand shares 90% of its insect pest species with that region. South east Australia has close trade and tourism links with New Zealand and because of its proximity a new incursion in that analogous climate should alert biosecurity authorities in New Zealand. -
Aphids (Hemiptera, Aphididae) Armelle Coeur D’Acier, Nicolas Pérez Hidalgo, Olivera Petrovic-Obradovic
Aphids (Hemiptera, Aphididae) Armelle Coeur d’Acier, Nicolas Pérez Hidalgo, Olivera Petrovic-Obradovic To cite this version: Armelle Coeur d’Acier, Nicolas Pérez Hidalgo, Olivera Petrovic-Obradovic. Aphids (Hemiptera, Aphi- didae). Alien terrestrial arthropods of Europe, 4, Pensoft Publishers, 2010, BioRisk, 978-954-642-554- 6. 10.3897/biorisk.4.57. hal-02824285 HAL Id: hal-02824285 https://hal.inrae.fr/hal-02824285 Submitted on 6 Jun 2020 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. A peer-reviewed open-access journal BioRisk 4(1): 435–474 (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2 435 doi: 10.3897/biorisk.4.57 RESEARCH ARTICLE BioRisk www.pensoftonline.net/biorisk Aphids (Hemiptera, Aphididae) Chapter 9.2 Armelle Cœur d’acier1, Nicolas Pérez Hidalgo2, Olivera Petrović-Obradović3 1 INRA, UMR CBGP (INRA / IRD / Cirad / Montpellier SupAgro), Campus International de Baillarguet, CS 30016, F-34988 Montferrier-sur-Lez, France 2 Universidad de León, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, 24071 – León, Spain 3 University of Belgrade, Faculty of Agriculture, Nemanjina 6, SER-11000, Belgrade, Serbia Corresponding authors: Armelle Cœur d’acier ([email protected]), Nicolas Pérez Hidalgo (nperh@unile- on.es), Olivera Petrović-Obradović ([email protected]) Academic editor: David Roy | Received 1 March 2010 | Accepted 24 May 2010 | Published 6 July 2010 Citation: Cœur d’acier A (2010) Aphids (Hemiptera, Aphididae). -
Seasonal Abundance of Acyrthosiphon Pisum (Harris) (Homoptera: Aphididae) and Therioaphis Trifola (Monell) (Homoptera: Callaphididae) on Lucerne in Central Greece1
ENTOMOLOGIA ÌIELLENICA 8 ( 1990): 41-46 Seasonal Abundance of Acyrthosiphon pisum (Harris) (Homoptera: Aphididae) and Therioaphis trifola (Monell) (Homoptera: Callaphididae) on Lucerne in Central Greece1 D. P. LYKOURESSIS and CH. P. POLATSIDIS Laboratory of Agricultural Zoology and Entomology, Agricultural University of Athens, 75 lera Odos, GR 118 55 Athens, Greece ABSTRACT Acyrthosiphonpisum (Harris) and Therioaphis trifolii (Monell) were the most abun dant aphid species on lucerne at Kopais, Co. Boiotia in central Greece from April 1984 to November 1986. Population fluctuations for A. pisum showed two peaks, the first during April-May and the second in November. Low numbers or zero were found during summer and till mid October as well as during winter and March. The abundance of this species during the year agrees generally with the effects of pre vailing temperatures in the region on aphid development and reproduction. T. tri fola also showed two population peaks but at different periods. The first occurred in July and the second from mid September to mid October. The first peak was higher than the second. The sharp decline in population densities that occurred in early August and lasted till mid September is not accounted for by adverse climatic conditions, but natural enemies and/or other limiting factors are possibly respon sible for that population reduction. Numbers were zero from December till March. while they kept at low levels during the rest of spring and part of June as well as from mid October till the end of November. Introduction species occurring quite frequently on lucerne in Several aphid species are known to attack temperate regions.