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Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(S): Diego J
Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(s): Diego J. Inclan and John O. Stireman, III Source: Annals of the Entomological Society of America, 104(2):287-296. Published By: Entomological Society of America https://doi.org/10.1603/AN10047 URL: http://www.bioone.org/doi/full/10.1603/AN10047 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. CONSERVATION BIOLOGY AND BIODIVERSITY Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States 1 DIEGO J. INCLAN AND JOHN O. STIREMAN, III Department of Biological Sciences, 3640 Colonel Glenn Highway, 235A, BH, Wright State University, Dayton, OH 45435 Ann. Entomol. Soc. Am. 104(2): 287Ð296 (2011); DOI: 10.1603/AN10047 ABSTRACT Although tachinids are one of the most diverse families of Diptera and represent the largest group of nonhymenopteran parasitoids, their local diversity and distribution patterns of most species in the family are poorly known. -
Wolbachia: a Friend Or Foe for Uzi Flies IS SN 2320-7078 JEZS 2014; 2 (2): 130-132 © 2014 JEZS B
Journal of Entomology and Zoology Studies 2014; 2(2): 130-132 Wolbachia: a friend or foe for Uzi flies IS SN 2320-7078 JEZS 2014; 2 (2): 130-132 © 2014 JEZS B. M. Prakash, A. Prathima, H. C. Huchesh, H. Ravikumar, H. P. Puttaraju Received: 08-02-2014 Accepted: 02-03-2014 1. Short Note B.M. Prakash The Uzi fly, Exorista sorbillans a tachinid endo-larval parasitoid of silkworm, Bombyx mori causes severe Evolutionary biology Laboratory, loss to the farming community of India. The exponential multiplication of this pest has alerted the number of Evolutionary and Organismal Biology scientist since three decades, though complete curable measures for this fly pest has not been investigated. In Unit, Jawaharlal Nehru Centre for this direction, scientists are investigating integrated approach for the management of the Uzi fly. Here we Advance Scientific Research, Jakkur, have investigated totally new approach for the management of the fly pest by using Wolbachia endobacteria [1-3] Bangalore – 560 064. Email: [email protected] The bacteria of the genus Wolbachia have been recently recognized to infect a wide range of arthropods Tel: +91-9008719144 including insects, mites, isopods and filarial nematodes [4, 5]. The intracellular bacteria were first reported from the culicine mosquitoes Culex pipiens by Hertig and Wolbach in the year 1924 and later named it as A. Prathima Wolbachia pipientis by Hertig in the year 1936 in the honor of his collaborator Wolbach. Later it was found Department of Biological Sciences, that, these bacteria were not only infects mosquitoes but also infects Drosophila and subsequently many Bangalore University, Bangalore- more insects. -
View the PDF File of the Tachinid Times, Issue 8
The Tachinid Times ISSUE 8 February 1995 Jim O'Hara, editor Agriculture & Agri-Food Canada, Biological Resources Division Centre for Land & Biological Resources Research C.E.F., Ottawa, Ontario, Canada, K1A 0C6 This issue marks the eighth year of The Tachinid Basic methodology: A team of (currently 9) Costa Rican Times. It is the largest issue so far, with the largest paraecologists range throughout all habitats night and mailing list as well (90). I hope you find this issue of day searching opportunistically and directedly for Lepid- interest. To keep this newsletter going, remember to optera larvae. These habitats are "wild", though they contribute some news from time to time. As usual, the represent the earliest stages of succession to virtually next issue will be distributed next February. undisturbed forest. When a caterpillar is found it is placed in a plastic bag with its presumed food (normally The Caterpillars and their Parasitoids of a Tropical this is the plant on which it was found). If it feeds, it is Dry Forest (by D.H. Janzen) then given a unique voucher number (e.g., 94-SRNP- Project name: The caterpillars and their parasitoids of 7857; this would be the 7857th caterpillar recorded in a tropical dry forest, Guanacaste Conservation Area, 1994; SRNP stands for Santa Rosa National Park, which northwestern Costa Rica. is today the Santa Rosa Sector of the GCA). That vou- Project goal: To determine the host-plant specificity of cher number is written on the plastic bag. The collection the entire set of macro caterpillars (and miners where information is recorded in field notebooks by the feasible) for the tropical dry forest in the Guanacaste collectors, and this information is later computer- Conservation Area in northwestern Costa Rica (0-300 m captured into a Filemaker Pro 2.0 flatfile database (de- elevation, six month dry season, total annual rainfall tails available on request). -
Diptera: Oestroidea) Magdi S
El-Hawagry Egyptian Journal of Biological Pest Control (2018) 28:46 Egyptian Journal of https://doi.org/10.1186/s41938-018-0042-3 Biological Pest Control RESEARCH Open Access Catalogue of the Tachinidae of Egypt (Diptera: Oestroidea) Magdi S. El-Hawagry Abstract Tachinid flies are an important group of parasitoids in their larval stage, and all their hosts are of the Arthropoda, almost exclusively other insects, including important insect pests in agriculture and forestry. All known Egyptian taxa of the family Tachinidae are systematically catalogued. Synonymies, type localities, type depositories, world distributions by biogeographic realm(s) and country, Egyptian localities, and dates of collection are provided. A total of 72 tachinid species belonging to 42 genera, 15 tribes, and 4 subfamilies has been treated. Keywords: Tachinid flies, Egyptian taxa, World distribution, Egyptian localities, Dates of collection Background agriculture and forestry. They typically parasitize phytopha- Tachinidae are a large and cosmopolitan family of flies gous larvae of Lepidoptera and Coleoptera or nymphs of within the superfamily Oestroidea. It is the second largest Hemiptera and Orthoptera. Consequently, tachinid flies family in the order Diptera (Irwin et al. 2003), with some have been successfully applied in programs of biological 1500 recognized genera (O’Hara 2016) and more than control against different insect pests (Stireman et al. 2006; 8500 described species (O’Hara 2013) worldwide. How- O’Hara 2008 and Cerretti and Tschorsnig 2010). ever, the estimated true diversity of the family is probably No comprehensive taxonomic studies on the family double the number of the currently known species, mak- Tachinidae have been carried out in Egypt before. -
L.) (Diptera: Tachinidae
Ph.D. thesis report Effect of short-term suboptimal temperature storage to assist large-scale production of Exorista larvarum (L.) (Diptera: Tachinidae) by Maurizio Benelli Department of Biological Sciences, Fauna Park, 205b Culloden Rd, Macquarie University, Sydney, NSW 2109, Australia. E-mail: [email protected] The thesis summary given below is based on my recently defended Ph.D. thesis entitled, “Effect of short-term sub- optimal temperature storage to assist large-scale production of two dipterans: Exorista larvarum (L.) and Bactrocera tryoni (Froggatt)”. This project was jointly administered by Alma Mater Studiorum Università di Bolo- gna (Italy) and Macquarie University (Sydney, Australia), with supervisors Prof. Maria Luisa Dindo (Bologna) and Prof. Phil Taylor (Sydney), and co-supervisor Dr. Fleur Ponton (Sydney). The thesis involved research on two dipterans: Exorista larvarum (L.) (Tachinidae) and Bactrocera tryoni (Frog- gatt) (Tephritidae). The focus below is on the tachinid, Exorista larvarum. Figure 1. A female Exorista lar- varum prepares to oviposit on a Galleria mellonella caterpil- lar. (Photo by Maurizio Benelli.) Thesis summary The rearing of insects has long been essential for many different purposes (research, pest management, obtainment of products such as honey, etc.) and the development of efficient rearing techniques and their refinement continue to be sought. Cold storage is a technique adopted for prolonging the developmental time of insects and thus increasing the efficiency of insect rearing. The advantages of cold storage protocols include a more flexible rearing schedule, the possibility to overcome periods of low production and, in case of beneficial insects, the synchronization of field releases with pest outbreaks in pest management programs. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
A Preliminary Study of the Diversity and Temporal Patterns of Abundance of Tachinidae in Southwestern Ohio
Wright State University CORE Scholar Biological Sciences Faculty Publications Biological Sciences 2-2009 A Preliminary Study of the Diversity and Temporal Patterns of Abundance of Tachinidae in Southwestern Ohio Diego J. Inclán John O. Stireman III Wright State University - Main Campus, [email protected] Follow this and additional works at: https://corescholar.libraries.wright.edu/biology Part of the Biology Commons, Ecology and Evolutionary Biology Commons, Entomology Commons, and the Systems Biology Commons Repository Citation Inclán, D. J., & Stireman, J. O. (2009). A Preliminary Study of the Diversity and Temporal Patterns of Abundance of Tachinidae in Southwestern Ohio. The Tachinid Times (22), 1-4. https://corescholar.libraries.wright.edu/biology/405 This Article is brought to you for free and open access by the Biological Sciences at CORE Scholar. It has been accepted for inclusion in Biological Sciences Faculty Publications by an authorized administrator of CORE Scholar. For more information, please contact [email protected]. The Tachinid Times ISSUE 22 February 2009 Jim O’Hara, editor Invertebrate Biodiversity Agriculture & Agri-Food Canada C.E.F., Ottawa, Ontario, Canada, K1A 0C6 Correspondence: [email protected] or [email protected] Last year’s issue of The Tachinid Times was items that are of special interest to persons involved in dedicated to Professor Chien-ming Chao of China, who tachinid research. Student submissions are particularly passed away in March 2007. Sadly, the year 2008 was welcome, especially abstracts from theses and accounts of similarly marked by the passing of a famous tachinidolo- studies in progress or about to begin. -
1 Modern Threats to the Lepidoptera Fauna in The
MODERN THREATS TO THE LEPIDOPTERA FAUNA IN THE FLORIDA ECOSYSTEM By THOMSON PARIS A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2011 1 2011 Thomson Paris 2 To my mother and father who helped foster my love for butterflies 3 ACKNOWLEDGMENTS First, I thank my family who have provided advice, support, and encouragement throughout this project. I especially thank my sister and brother for helping to feed and label larvae throughout the summer. Second, I thank Hillary Burgess and Fairchild Tropical Gardens, Dr. Jonathan Crane and the University of Florida Tropical Research and Education center Homestead, FL, Elizabeth Golden and Bill Baggs Cape Florida State Park, Leroy Rogers and South Florida Water Management, Marshall and Keith at Mack’s Fish Camp, Susan Casey and Casey’s Corner Nursery, and Michael and EWM Realtors Inc. for giving me access to collect larvae on their land and for their advice and assistance. Third, I thank Ryan Fessendon and Lary Reeves for helping to locate sites to collect larvae and for assisting me to collect larvae. I thank Dr. Marc Minno, Dr. Roxanne Connely, Dr. Charles Covell, Dr. Jaret Daniels for sharing their knowledge, advice, and ideas concerning this project. Fourth, I thank my committee, which included Drs. Thomas Emmel and James Nation, who provided guidance and encouragement throughout my project. Finally, I am grateful to the Chair of my committee and my major advisor, Dr. Andrei Sourakov, for his invaluable counsel, and for serving as a model of excellence of what it means to be a scientist. -
The Tachinid Times
The Tachinid Times ISSUE 24 February 2011 Jim O’Hara, editor Invertebrate Biodiversity Agriculture & Agri-Food Canada ISSN 1925-3435 (Print) C.E.F., Ottawa, Ontario, Canada, K1A 0C6 ISSN 1925-3443 (Online) Correspondence: [email protected] or [email protected] My thanks to all who have contributed to this year’s announcement before the end of January 2012. This news- issue of The Tachinid Times. This is the largest issue of the letter accepts submissions on all aspects of tachinid biology newsletter since it began in 1988, so there still seems to be and systematics, but please keep in mind that this is not a a place between peer-reviewed journals and Internet blogs peer-reviewed journal and is mainly intended for shorter for a medium of this sort. This year’s issue has a diverse news items that are of special interest to persons involved assortment of articles, a few announcements, a listing of in tachinid research. Student submissions are particularly recent literature, and a mailing list of subscribers. The welcome, especially abstracts of theses and accounts of Announcements section is more sizable this year than usual studies in progress or about to begin. I encourage authors and I would like to encourage readers to contribute to this to illustrate their articles with colour images, since these section in the future. This year it reproduces the abstracts add to the visual appeal of the newsletter and are easily of two recent theses (one a Ph.D. and the other a M.Sc.), incorporated into the final PDF document. -
Zooj(J))Gicaj1 Short Note 0J1I!Jj](Dli(F}§
Zoological Studies 34(1) 62-66 (1995) Zooj(j))gicaJ1 Short Note 0J1I!Jj](dli(f}§ Surface Morphology of Egg Chorion of the Uzi Fly, Exorista bombycis (Louis), (Diptera: Tachinidae) - an Endoparasite of the Silkworm, Bombyx mori Linn. Sunil K. Tewari ' , Vineet Kumar, Arvind K. Awasthi and Rajat K. Datta Electron Microscopy Unit, Central Sericultural Research and Training Institute, Mysore - 570008, India (Accepted July 1, 1994) ., Sunil K. Tewari, Vineet Kumar, Arv ind K. Aw asthi and Rajat K. Datt a (1995) Surface morphology of egg chorion of the Uzi fly, Exorista bombycis (Louis), (Diptera: Tachinidae) - an endoparasite of the silkworm, Bombyx mori Linn . Zoological Studies 34(1): 62-66. Scanning electron microscope observations on the egg chorio n of the Uzi fly Exorista bombycis (Louis) (Diptera : Tachinidae) were carried out to obtain further understanding -of the probable function and developm ent of chor ionic structures of eggs. The study reveals morphologically and physiologically important structures viz. aeropyles, micropyles, a circular lid with a well defined hatch ing line, a chorionic respiratory network, etc. The egg of E. bombycis is considered indehiscent, i.e., the egg chorion is not modified for hatchin g and the larva emerges from the ventral egg surface. However , a lid surrounded by a well defined hatching line is present in E. bombycis, but is genera lly found in dehiscent Tach inid eggs and is used for hatching . Further, the type of chorionic respiratory systems in the family Tachin idae are discussed in detail. Key wo rds: Eggshell, Chorionic respiratory system, Hatching line, Uzi fly, Scanning electron microscope. -
Tachinid Collecting in the Rocky Mountains of Western Montana, U.S.A
Figure 1. Juan Manuel (left) and John (right) search for tachinids at Hoodoo Pass on the Montana- Idaho border in the Bitterroot Range of the Rocky Mountains. Tachinid collecting in the Rocky Mountains of Western Montana, U.S.A. by John O. Stireman III1 , James E. O’Hara2 and Juan M. Perilla López1 1 Department of Biological Sciences, Wright State University, 3640 Colonel Glenn Highway, Dayton, Ohio 45435, USA. E-mails: [email protected], [email protected] 2 Canadian National Collection of Insects, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario, K1A 0C6, Canada. E-mail: [email protected] In June of 2017, the Field Meeting of the North American Dipterists Society (NADS) was held at the Lubrecht Experimental Forest in western Montana, U.S.A. NADS field meetings, held every two years, provide an opportu- nity for the Diptera research community to meet with their colleagues, collect flies in interesting locales, and learn about current research projects of participants during evening talks. Each meeting is held at a different field site in North America that provides access to a variety of habitats for collecting. An overview of the 2017 meeting in Montana, written by the organizer Andrew Fasbender, can be found in Fly Times issue 59 (Fasbender 2017). Here, we report on the tachinid fauna of the area collected by John Stireman, Jim O’Hara and Juan Manuel Perilla López (accompanied by fellow collector and oestroidiphile Greg Dahlem; see the four of us on the cover of this issue of The Tachinid Times). Collecting Sites ur collecting was conducted in the Rocky Mountains of western Montana, in the vicinity of the city of Missou- Ola (Fig. -
The Temperature-Dependent Development Of
Short Communication KOREAN JOURNAL OF APPLIED ENTOMOLOGY 한국응용곤충학회지 ⓒ The Korean Society of Applied Entomology Korean J. Appl. Entomol. 55(4): 445-452 (2016) pISSN 1225-0171, eISSN 2287-545X DOI: http://dx.doi.org/10.5656/KSAE.2016.09.0.054 항온조건에서 긴등기생파리 [Exorista japonica (Townsend)] (Diptera: Tachinidae) 온도별 발육 박창규*ㆍ서보윤ㆍ최병렬 국립농업과학원 농산물안전성부 작물보호과 The Temperature-Dependent Development of the Parasitoid Fly, Exorista Japonica (Townsend) (Diptera: Tachinidae) Chang-Gyu Park*, Bo Yoon Seo and Byeong-Ryoel Choi Crop Protection Division, Department of Agro-Food Safety and Crop Protection, National Institute of Agricultural Sciences, Wanju 55365, Republic of Korea ABSTRACT: Exorista japonica is one of the major natural enemies of noctuid larvae, Mythimna separata and Spodoptera litura. The examined parasitoid was obtained from host species M. separata, collected at Gimje city and identified by DNA sequences (partial cytochrome oxidase I, 16S, 18S, and 28S). For purposed of this study, laboratory reared S. litura served as the host species for the development of the E. japonica. The developmental period of E. japonica immature stages were investigated at seven constant temperatures (16, 19, 22, 25, 28, 31, 34±1℃, RH 20∼30%). Temperature-dependent developmental rates and development completion models were developed. E. japonica was successfully developed from egg to adult in 16∼31℃ temperature regimes. Developmental duration was the shortest at 34℃ (8.3 days) and the longest at 16℃ (23.4 days) from egg to pupa development. Pupal development duration was the shortest at 28℃ (7.3 days). Total immature-stage development duration decreased with increasing temperature, and was the shortest at 31℃ (16.3 days) and the longest at 16℃ (45.4 days).