Flower Flies (Syrphidae) and Other Biological Control Agents for Aphids in Vegetable Crops
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Larval Dispersal Behaviour and Survival on Non-Prey Food of The
Ecological Entomology (2018), 43, 578–590 DOI: 10.1111/een.12636 Dealing with food shortage: larval dispersal behaviour and survival on non-prey food of the hoverfly Episyrphus balteatus ILKA VOSTEEN,∗ JONATHAN GERSHENZON and GRIT KUNERT Department of Biochemistry, Max-Planck Institute for Chemical Ecology, Jena, Germany Abstract. 1. Predatory larvae often have to face food shortages during their develop- ment, and thus the ability to disperse and find new feeding sites is crucial for survival. However, the dispersal capacity of predatory larvae, the host finding cues employed, and their use of alternative food sources are largely unknown. These aspects of the foraging behaviour of the aphidophagous hoverfly (Episyrphus balteatus De Geer) larvae were investigated in the present study. 2. It was shown that these hoverfly larvae do not leave a plant as long as there are aphids available, but that dispersing larvae are able to find other aphid colonies in the field. Dispersing hoverfly larvae accumulated on large aphid colonies, but did not distinguish between different pea aphid race–plant species combinations. Large aphid colonies might be easier to detect because of intensified searching by hoverfly larvae following the encounter of aphid cues like honeydew that accumulate around large colonies. 3. It was further shown that non-prey food, such as diluted honey or pollen, was insufficient for hoverfly larvae to gain weight, but prolonged the survival of thelarvae compared with unfed individuals. As soon as larvae were switched back to an aphid diet, they rapidly gained weight and some pupated after a few days. Although pupation and adult hatching rates were strongly reduced compared with hoverflies continuously fed with aphids, the consumption of non-prey food most probably increases the probability that hoverfly larvae find an aphid colony and complete their development. -
Diptera: Syrphidae
This is a repository copy of The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae).. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/80035/ Version: Accepted Version Article: Penney, HD, Hassall, C orcid.org/0000-0002-3510-0728, Skevington, JH et al. (2 more authors) (2014) The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae). The American Naturalist, 183 (2). pp. 281-289. ISSN 0003-0147 https://doi.org/10.1086/674612 Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae)1 Heather D. Penney, Christopher Hassall, Jeffrey H. Skevington, Brent Lamborn & Thomas N. Sherratt Abstract Palatable (Batesian) mimics of unprofitable models could use behavioral mimicry to compensate for the ease with which they can be visually discriminated, or to augment an already close morphological resemblance. -
Research Article Ecological Observations of Native Geocoris Pallens and G
Hindawi Publishing Corporation Psyche Volume 2013, Article ID 465108, 11 pages http://dx.doi.org/10.1155/2013/465108 Research Article Ecological Observations of Native Geocoris pallens and G. punctipes Populations in the Great Basin Desert of Southwestern Utah Meredith C. Schuman, Danny Kessler, and Ian T. Baldwin Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Hans-Knoll-Straße¨ 8, 07745 Jena, Germany Correspondence should be addressed to Ian T. Baldwin; [email protected] Received 5 November 2012; Accepted 16 April 2013 Academic Editor: David G. James Copyright © 2013 Meredith C. Schuman et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Big-eyed bugs (Geocoris spp. Fallen,´ Hemiptera: Lygaeidae) are ubiquitous, omnivorous insect predators whose plant feeding behavior raises the question of whether they benefit or harm plants. However, several studies have investigated both the potential of Geocoris spp. to serve as biological control agents in agriculture and their importance as agents of plant indirect defense in nature. These studies have demonstrated that Geocoris spp. effectively reduce herbivore populations and increase plant yield. Previous work has also indicated that Geocoris spp. respond to visual and olfactory cues when foraging and choosing their prey and that associative learning of prey and plant cues informs their foraging strategies. For these reasons, Geocoris spp. have become models for the study of tritrophic plant-herbivore-predator interactions. Here, we present detailed images and ecological observations of G. pallens Stal˚ and G. -
Insecticideinduced Hormesis and Arthropod Pest Management
Review Received: 31 August 2013 Revised: 7 October 2013 Accepted article published: 23 October 2013 Published online in Wiley Online Library: 2 December 2013 (wileyonlinelibrary.com) DOI 10.1002/ps.3669 Insecticide-induced hormesis and arthropod pest management Raul Narciso C Guedesa∗ and G Christopher Cutlerb Abstract Ecological backlashes such as insecticide resistance, resurgence and secondary pest outbreaks are frequent problems associated with insecticide use against arthropod pest species. The last two have been particularly important in sparking interest in the phenomenon of insecticide-induced hormesis within entomology and acarology. Hormesis describes a biphasic dose–response relationship that is characterized by a reversal of response between low and high doses of a stressor (e.g. insecticides). Although the concept of insecticide-induced hormesis often does not receive sufficient attention, or has been subject to semantic confusion, it has been reported in many arthropod pest species and natural enemies, and has been linked to pest outbreaks and potential problems with insecticide resistance. The study of hormesis remains largely neglected in entomology and acarology. Here, we examined the concept of insecticide-induced hormesis in arthropods, its functional basis and potential fitness consequences, and its importance in arthropod pest management and other areas. c 2013 Society of Chemical Industry Keywords: biphasic concentration–response; hormoligosis; insecticidal stress; insecticide ecotoxicology; pesticide-mediated homeostatic regulation; sublethal effects 1 HORMESIS: ANCIENT ADAGES, OLD LAWS group recognized the general nature of the phenomenon in a suc- AND CURRENT THEORY cession of meta-analyses.9–13 They suggested that the hormetic Friedrich Nietzsche in his Twilight of the Idols (1888) expressed dose–response model is more common in toxicology than the threshold model (Fig. -
Syrphid Flies
Published by Utah State University Extension and Utah Plant Pest Diagnostic Laboratory Ent-200-18PR February 2019 Beneficial Predators: Syrphid Flies Steven Price, Carbon Co. Extension • Ron Patterson, University of Idaho, Bonneville Co. Extension DESCRIPTION What you should know Eggs are oblong, white or grey with a lace-like pattern • Syrphid flies are common residents in agricultural on the surface, and measure around 1/16 inch long. areas, gardens, and home landscapes providing They are laid singly on plants often near dense colonies pollination services. of prey which are located by females by olfactory, • Larvae of syrphid flies are important beneficial visual, and tactile cues. predators of soft-bodied pests providing naturally Larvae can be found living among their prey, although occurring pest control. are sometimes misidentified as pests, such as sawfly • Syrphid flies cannot be purchased commercially larvae, slugs, alfalfa weevil larvae, or different kinds of but populations can be conserved by reducing caterpillars (Table 1). Syrphid fly larvae have a tapered broad-spectrum pesticide use. anterior which lacks an external head capsule. The flattened rear has two small breathing holes (spiracles). Larvae are semi-translucent, often being striped or Syrphid (pronounced ‘sir-fid’) flies, also known as hover mottled in shades of white, green, tan, or brown with flies or flower flies, commonly occur in field crops, additional small bumps or spikes (Fig. 1). Being 1/16 inch orchards, gardens and home landscapes. They are long upon hatching, they are typically less than 1/2 inch members of the Syrphidae family. They are “true flies” long once they are full-sized. -
A Comparative Study of Two Seed Bugs, Geocoris
A COMPARATIVE STUDY OF TWO SEED BUGS, GEOCORIS BULLATUS (SAY) AND G. DISCOPTERUS STAL (HEMIPTERA: LYGAEIDAE) IN THE YUKON. By JENNIFER J. ROBINSON B.Sc. Trent University, 1980 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE in THE FACULTY OF GRADUATE STUDIES DEPARTMENT OF ZOOLOGY We accept this thesis as conforming te trie required standard June, 1985 (c) Jennifer J. Robinson, 1985 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department of The University of British Columbia 1956 Main Mall Vancouver, Canada V6T 1Y3 )E-6 C3/81) Abstract Geocoris bullatus (Say 1831), (Henriptera: Lygaeidae) has been collected and studied across North America but the present work is the o first detailed study of western North American CL discopterus Stal 1874. In fact, it has been claimed that 6^. discopterus is solely a species of the east. As the two species are taxonomically difficult to separate, when they were apparently discovered together at several localities in the southwestern Yukon, a detailed investigation of their systematics and distribution seemed necessary. Species status of Yukon Q. bullatus and iG. -
Conservation Biological Control of Rosy Apple Aphid, Dysaphis Plantaginea (Passerini), in Eastern North America
COMMUNITY AND ECOSYSTEM ECOLOGY Conservation Biological Control of Rosy Apple Aphid, Dysaphis plantaginea (Passerini), in Eastern North America 1 2 M. W. BROWN AND CLARISSA R. MATHEWS Environ. Entomol. 36(5): 1131Ð1139 (2007) ABSTRACT Because of the potentially serious damage rosy apple aphid, Dysaphis plantaginea (Passerini) (Homoptera: Aphididae), can cause to apple fruit and branch development, prophylactic insecticides are often used for control. If biological control could be relied on, the amount of pesticide applied in orchards could be reduced. This study examined biological control of rosy apple aphid in eastern West Virginia and the potential for enhancement through conservation biological control, in particular, the effect of interplanting extraßoral nectar-bearing peach trees. By 20 d after Þrst bloom, only 2% of fundatrices initially present survived to form colonies based on regression of data from 687 colonies. Exclusion studies showed that many of the early colonies were probably destroyed by predation; the major predator responsible seemed to be adult Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae). Mortality before apple bloom was most important in controlling rosy apple aphid population growth but by itself is not sufÞciently reliable to prevent economic injury. Interplanting of extraßoral nectar-bearing trees did not increase biological control, and interplanting with 50% trees with extraßoral nectar glands reduced biological control. The number of leaf curl colonies in the 50% interplanted orchards was lower than in monoculture orchards, suggesting a preference of alate oviparae for more diverse habitats, supporting the resource concentration hypothesis but not at a level sufÞcient to prevent injury. Predation and parasitism after the formation of leaf curl colonies was not adequate to control rosy apple aphid populations. -
Aromatic Plants of East Asia to Enhance Natural Enemies Towards Biological Control of Insect Pests
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/331989081 Aromatic plants of East Asia to enhance natural enemies towards biological control of insect pests. A review Article in Entomologia Generalis · March 2019 DOI: 10.1127/entomologia/2019/0625 CITATIONS READS 2 242 4 authors: Séverin Hatt Qingxuan Xu Kyoto University University of Liège 35 PUBLICATIONS 231 CITATIONS 24 PUBLICATIONS 62 CITATIONS SEE PROFILE SEE PROFILE Frédéric Francis Naoya Osawa University of Liège Kyoto University 427 PUBLICATIONS 4,800 CITATIONS 78 PUBLICATIONS 1,050 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Termitofuel View project Interaction between piercing-sucking insects and their host plants : focus on salivary proteome and feeding behavior View project All content following this page was uploaded by Séverin Hatt on 26 March 2019. The user has requested enhancement of the downloaded file. Aromatic plants of East Asia to enhance natural enemies towards biological control of insect pests. A review Séverin HATT1,2*, Qingxuan XU3, Frédéric FRANCIS4, Naoya OSAWA1 This paper has been published in Entomologia Generalis: https://www.schweizerbart.de/papers/entomologia/detail/38/90582/Aromatic_plants_of_East_ Asia_to_enhance_natural_enemies_towards_biological_control_of_insect_pests_A_review To cite: Hatt S., Xu Q., Francis F., Osawa N. (2019). Aromatic plants of East Asia to enhance natural enemies towards biological control of -
Kobor Peter Dissertation.Pdf
1 PANNON EGYETEM GEORGIKON KAR KESZTHELY Festetics Doktori Iskola Iskolavezető: Dr. Anda Angéla, DSc. Állattudományi Tanszék DOKTORI (PH.D.) ÉRTEKEZÉS INVESTIGATIONS ON THE TAXONOMY AND SYSTEMATICS OF BIG-EYED BUGS (HETEROPTERA: LYGAEOIDEA: GEOCORIDAE) Témavezető: Dr. habil. Kondorosy Előd CSc, egyetemi tanár Készítette: Kóbor Péter Keszthely, 2020 2 INVESTIGATIONS ON THE TAXONOMY AND SYSTEMATICS OF BIG-EYED BUGS (HETEROPTERA: LYGAEOIDEA: GEOCORIDAE) Értekezés doktori (PhD) fokozat elnyerése érdekében Írta: Kóbor Péter Készült a Pannon Egyetem Festetics Doktori Iskola keretében Témavezető: Dr. Kondorosy Előd Elfogadásra javaslom (igen / nem) ……………………………….(aláírás) A jelölt a doktori szigorlaton ........%-ot ért el, Az értekezést bírálóként elfogadásra javaslom: Bíráló neve: …........................ …................. igen /nem ………………………. (aláírás) Bíráló neve: …........................ ….................) igen /nem ………………………. (aláírás) ***Bíráló neve: …........................ ….................) igen /nem ………………………. (aláírás) A jelölt az értekezés nyilvános vitáján …..........%-ot ért el. A doktori (PhD) oklevél minősítése…................................. ………………………… Az EDHT elnöke 3 TABLE OF CONTENT 1. Abstracts .............................................................................................................................................. 6 1.1. Abstract ........................................................................................................................................ 6 1.2. Kivonat ........................................................................................................................................ -
Articles & Book Reviews
Newsletter of the Colorado Native Plant Society ARTICLES & BOOK REVIEWS Marr Steinkamp Research: Pollination Biology of the Stream Orchid Alpine Cushion Plants in New Zealand Interview with Barbara Fahey, Native Plant Master® Program Founder Conservation Corner: White River Beardtongue How Lupines Talk to Bees Volume 38, No. 2 Summer 2014 Aquilegia: Newsletter of the Colorado Native Plant Society Dedicated to furthering the knowledge, appreciation, and conservation of native plants and habitats of Colorado through education, stewardship, and advocacy Volume 38 Number 2 Summer 2014 ISSN 2161-7317 (Online) - ISSN 2162-0865 (Print) Inside this issue News & Announcements................................................................................................ 3 Field Trips........................................................................................................................6 Articles Marr/Steinkamp Research: Pollination Biology of Epipactis gigantea........................9 How Lupines Talk to Bees...........................................................................................11 The Other Down Under: Exploring Alpine Cushion Plants in New Zealand...........14 The Native Plant Master® Program: An Interview with Barbara Fahey.....................16 Conservation Corner: White River Beardtongue......................................................... 13 Book & Media Reviews, Song........................................................................................19 Calendar...................................................................................................................... -
Companion Planting and Insect Pest Control
Chapter 1 Companion Planting and Insect Pest Control Joyce E. Parker, William E. Snyder, George C. Hamilton and Cesar Rodriguez‐Saona Additional information is available at the end of the chapter http://dx.doi.org/10.5772/55044 1. Introduction There is growing public concern about pesticides’ non-target effects on humans and other organisms, and many pests have evolved resistance to some of the most commonly-used pesticides. Together, these factors have led to increasing interest in non-chemical, ecologically- sound ways to manage pests [1]. One pest-management alternative is the diversification of agricultural fields by establishing “polycultures” that include one or more different crop varieties or species within the same field, to more-closely match the higher species richness typical of natural systems [2, 3]. After all, destructive, explosive herbivore outbreaks typical of agricultural monocultures are rarely seen in highly-diverse unmanaged communities. There are several reasons that diverse plantings might experience fewer pest problems. First, it can be more difficult for specialized herbivores to “find” their host plant against a back‐ ground of one or more non-host species [4]. Second, diverse plantings may provide a broader base of resources for natural enemies to exploit, both in terms of non-pest prey species and resources such as pollen and nectar provided by the plant themselves, building natural enemy communities and strengthening their impacts on pests [4]. Both host-hiding and encourage‐ ment of natural enemies have the potential to depress pest populations, reducing the need for pesticide applications and increasing crop yields [5, 6]. On the other hand, crop diversification can present management and economic challenges for farmers, making these schemes difficult to implement. -
Baccha (Ocyptamus) Medina, B
The Syrphidae of Puerto Rico1'2 H. S. Telford3-* One cannot state with certainty when the first syrphid was collected from Puerto Rico and adjacent islands. Fabricius described a number of 1 Manuscript submitted to Editorial Board October 30, 1972. 2 Scientific paper number 3914. College of Agriculture Research Center, Washing ton State University, Pullman, Washington. Work was conducted under Project No. 0046. 3 Professor and Entomologist, Department of Entomology, Washington State University; Visiting Scientist, Department of Entomology, Agricultural Experiment Station, Mayagiiez Campus, Uío Piedras, Puerto Rico, September 1968-March 1969. This study was made possible by financial support from the Department of En tomology, Agricultural Experiment Station, Mayagiiez Campus, University of Puerto Rico, Río Piedras. I wish to thank Dr. L. P. R. F. Martorell, formerly Chairman, Department of Entomology, Agricultural Experiment Station, especially for his support and aid in all aspects of the project. Mr. Silverio Medina Gaud, Associate Entomologist, Agricultural Experiment Station, was of considerable help. He ac companied me on almost all field trips, assisted in sorting and preparing the material and made valuable field trips on his own. Dr. J. R. Vockeroth, Entomology Research Institute, Ottawa, Canada, verified many determinations and offered advice on nomenclatural problems. Others who materially aided in the loan of specimens, verified determinations or in other ways were: Dr. George Drury, U.S. Atomic Energy Commission, El Verde-Caribbean National Forest, Puerto Rico; Dr. Y. S. Sedman, Western Illinois University; Dr. L. V. Knutson, Systematic Entomology Laboratory, Agricultural Research Service, United States Department of Agriculture; Dr. P. W. Wygodzinsky, American Museum of Natural History; Dr.