PPRI News, No 112, April-September 2018
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Comparative Water Relations of Adult and Juvenile Tortoise Beetles: Differences Among Sympatric Species
Comparative Biochemistry and Physiology Part A 135 (2003) 625–634 Comparative water relations of adult and juvenile tortoise beetles: differences among sympatric species Helen M. Hull-Sanders*, Arthur G. Appel, Micky D. Eubanks Department of Entomology and Plant Pathology, Auburn University, 301 Funchess Hall, Auburn, AL 36849-5413, USA Received 5 February 2003; received in revised form 20 May 2003; accepted 20 May 2003 Abstract Relative abundance of two sympatric tortoise beetles varies between drought and ‘wet’ years. Differing abilities to conserve water may influence beetle survival in changing environments. Cuticular permeability (CP), percentage of total body water (%TBW), rate of water loss and percentage of body lipid content were determined for five juvenile stages and female and male adults of two sympatric species of chrysomelid beetles, the golden tortoise beetle, Charidotella bicolor (F. ) and the mottled tortoise beetle, Deloyala guttata (Olivier). There were significant differences in %TBW and lipid content among juvenile stages. Second instars had the greatest difference in CP (37.98 and 11.13 mg cmy2 hy1 mmHgy1 for golden and mottled tortoise beetles, respectively). Mottled tortoise beetles had lower CP and greater %TBW compared with golden tortoise beetles, suggesting that they can conserve a greater amount of water and may tolerate drier environmental conditions. This study suggests that juvenile response to environmental water stress may differentially affect the survival of early instars and thus affect the relative abundance of adult beetles in the field. This is supported by the low relative abundance of golden tortoise beetle larvae in a drought year and the higher abundance in two ‘wet’ years. -
Do Fecal Shields and Herbivore-Caused Volatiles Match Host Plant Chemical Profiles?
Chemoecology (2013) 23:1–11 DOI 10.1007/s00049-012-0117-7 CHEMOECOLOGY RESEARCH PAPER Making scents of defense: do fecal shields and herbivore-caused volatiles match host plant chemical profiles? Ken Keefover-Ring Received: 18 March 2012 / Accepted: 26 September 2012 / Published online: 13 October 2012 Ó Springer Basel 2012 Abstract Many plant families have aromatic species that shields and volatile emissions are influenced by the produce volatile compounds which they release when amounts and volatilities of compounds present in the host damaged, particularly after suffering herbivory. Monarda plant. The implications of these results are explored for the fistulosa (Lamiaceae) makes and stores volatile essential chemical ecology of both the plant and the insect. oils in peltate glandular trichomes on leaf and floral sur- faces. This study examined the larvae of a specialist Keywords Aromatic plants Á Herbivore-caused volatiles Á tortoise beetle, Physonota unipunctata, which feed on two Larval fecal shields Á Monarda fistulosa Á M. fistulosa chemotypes and incorporate host compounds Physonota unipunctata Á Terpenoids into fecal shields, structures related to defense. Compari- sons of shield and host leaf chemistry showed differences between chemotypes and structures (leaves vs. shields). Introduction Thymol chemotype leaves and shields contained more of all compounds that differed than did carvacrol chemotypes, Plants emit volatiles when fed upon by insects. The vola- except for carvacrol. Shields had lower levels of most of tiles resulting from herbivory for many plant species the more volatile chemicals than leaves, but more than consist of various mono- and sesquiterpenoids, heterocy- twice the amounts of the phenolic monoterpenes thymol clic compounds such as indole, and saturated and and carvacrol and greater totals. -
21 March 2017 CURRICULUM VITAE Barry M. Oconnor Personal Born
21 March 2017 CURRICULUM VITAE Barry M. OConnor Personal Born November 9, 1949, Des Moines, Iowa, USA Citizenship: USA. Education Michigan State University, 1967-69. Major: Biology. Iowa State University, 1969-71. B.S. Degree, June, 1971, awarded with Distinction. Major: Zoology; Minors: Botany, Education. Cornell University, 1973-79. Ph.D. Degree, August, 1981. Major Subject: Acarology; Minor Subjects: Insect Taxonomy, Vertebrate Ecology. Professional Employment Research Zoologist, Department of Zoology, University of California, Berkeley, California; October, 1979 - September, 1980. Assistant Professor of Biology/Assistant Curator of Insects, Museum of Zoology, University of Michigan, Ann Arbor, Michigan; October, 1980 - December, 1986. Associate Professor of Biology/Associate Curator of Insects, Museum of Zoology, University of Michigan, Ann Arbor, Michigan; January, 1987 - April 1999. Professor of Biology/Curator of Insects, Museum of Zoology, University of Michigan, Ann Arbor, Michigan; September 1999 - June 2001. Professor of Ecology and Evolutionary Biology/Curator of Insects, Museum of Zoology, University of Michigan, Ann Arbor, Michigan; July 2001-present Visiting Professor, Escuela Nacional de Ciencias Biologicas, Instituto Politecnico Nacional, Mexico City, Mexico; January-February, 1985. Visiting Professor, The Acarology Summer Program, Ohio State University, Columbus, Ohio; June-July 1980 - present. Honors, Awards and Fellowships National Merit Scholar, 1967-71. B.S. Degree awarded with Distinction, 1971. National Science Foundation Graduate Fellowship, 1973-76. Cornell University Graduate Fellowship, 1976-77. 2 Tawfik Hawfney Memorial Fellowship, Ohio State University, 1977. Outstanding Teaching Assistant, Cornell University Department of Entomology, 1978. President, Acarological Society of America, 1985. Fellow, The Willi Hennig Society, 1984. Excellence in Education Award, College of Literature, Science and the Arts, University of Michigan, 1995 Keynote Speaker, Acarological Society of Japan, 1999. -
Diversity and Altitudinal Distribution of Chrysomelidae (Coleoptera) in Peregrina Canyon, Tamaulipas, Mexico
A peer-reviewed open-access journal ZooKeysDiversity 417: 103–132 and (2014) altitudinal distribution of Chrysomelidae (Coleoptera) in Peregrina Canyon... 103 doi: 10.3897/zookeys.417.7551 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research Diversity and altitudinal distribution of Chrysomelidae (Coleoptera) in Peregrina Canyon, Tamaulipas, Mexico Uriel Jeshua Sánchez-Reyes1, Santiago Niño-Maldonado2, Robert W. Jones3 1 División de Estudios de Posgrado e Investigación. Instituto Tecnológico de Cd. Victoria. Boulevard Emilio Portes Gil No.1301, C.P. 87010. Ciudad Victoria, Tamaulipas, México 2 Facultad de Ingeniería y Cien- cias. Universidad Autónoma de Tamaulipas. Centro Universitario Victoria. CP. 87149. Victoria, Tamaulipas, México 3 Facultad de Ciencias Naturales. Universidad Autónoma de Querétaro. Avenida de las Ciencias, s/n, 76230 Juriquilla, Querétaro, México Corresponding author: Santiago Niño-Maldonado (email address) Academic editor: A. Konstantinov | Received 19 March 2014 | Accepted 27 May 2014 | Published 19 June 2014 http://zoobank.org/D8630AC3-E81B-4C9B-94A6-F69E1F596BFC Citation: Sánchez-Reyes UJ, Niño-Maldonado S, Jones RW (2014) Diversity and altitudinal distribution of Chrysomelidae (Coleoptera) in Peregrina Canyon, Tamaulipas, Mexico. ZooKeys 417: 103–132. doi: 10.3897/zookeys.417.7551 Abstract The Chrysomelidae (Coleoptera) is a highly speciose family that has been poorly studied at the region- al level in Mexico. In the present study, we estimated species richness and diversity in oak-pine forest, Tamaulipan thorny scrub and in tropical deciduous forests in Peregrina Canyon within the Altas Cumbres Protected Area of the northeastern state of Tamaulipas, Mexico. Sampling of Chrysomelidae consisted of five sweep net samples (200 net sweeps) within each of three sites during four sample periods: early dry season, late dry season, early wet season, and late wet season. -
8. Parasitology the Diversity and Specificity of Parasitoids Attacking
8. Parasitology The diversity and specificity of parasitoids attacking Neotropical tortoise beetles (Chrysomelidae, Cassidinae) Marie Cuignet1, Donald Windsor2, Jessica Reardon3 and Thierry Hance4 Abstract. Tortoise beetles have numerous adaptations to keep enemies at bay - in- cluding tightly-aggregated larvae that move synchronously about the food plant, construction of predator-deterring exuvio-fecal shields, maternal guarding of im- matures, and adults that pull their carapace flush to the leaf to escape enemies. Despite these and other adaptations this subfamily of Chrysomelidae has been re- garded as one of the most heavily parasitized. To better describe the impact and diversity of the parasitoid community which successfully evades these defenses we collected and reared the immature and adult stages of 47 species of Panamanian Cassidinae obtaining at least 41 species of parasitoids. Over half of the species ob- tained (26) were egg parasitoids (Eulophidae, Entedoninae), 20 of those Emersonella species, 13 undescribed at the time of the study. Phoresy was confirmed in at least six Emersonella species, two of which emerged from the eggs of 11 and 13 different host species. Nevertheless, the majority of Eulophidae species (15 of 26) were reared from a single host. Additionally, five species of Chalcidae, eight species of Tachinidae, two Nematomorpha and the lepidopteran, Schacontia sp. (Crambidae) were obtained from rearings of larvae, pupae and adults. One tachinid species (Eucelatoria sp.) in- fected the larval stage of Chelymorpha alternans, and was found in the abdomens of 27.6 percent of dissected adults. Keywords. Cassidinae, Eulophidae, Tachinidae, parasitoids, parasitism. 1 Unite d'ecologie et de biogeographie, Centre de recherche sur la biodiversite, 4 et 5 Place Croix-du-Sud, 1348 Louvain-la-Neuve. -
And Physonota Alutacea Boheman (Coleoptera: Chrysomelidae: Cassidinae)
ANN ALES ZOOLOGICI (Warszawa), 2008, 58(3): 641 -665 IMMATURE STAGES OF ASTEBIZA FLAVICORNIS (OLIVIER) AND PHYSONOTA ALUTACEA BOHEMAN (COLEOPTERA: CHRYSOMELIDAE: CASSIDINAE) JOLANTA SWILTOJANSKA1 and DONALD M. WINDSOR2 ^Zoological Institute, University of Wroclaw, Przybyszewskiego 63/77, 51-148 Wroclaw, Poland; e-mail: [email protected] (author for correspondence) ^-Smithsonian Tropical Research Institute, Apartado 0843-03092, Panama, Republica de Panama; e-mail: [email protected] Abstract.— The first instar larva oiPhysonota alutacea Boheman, 1854, a member of the tribe Physonotini Spaeth, 1942, and the mature larva and pupa of Asteriza flavicornis (Olivier, 1790), a member of the tribe Asterizini Hincks, 1952, are described for the first time. The mature larva and the pupa oiPhysonota alutacea are redescribed. Immatures are figured and described using light microscopy, the first instar larva of Physonota alutacea using scanning electron microscopy. Similarities in the larval morphologies of Cistudinella Champion, 1894, a member of the tribe Ischyrosonychini, Chapuis, 1875, and Physonota suggest both genera are close phylogenetically and should be placed in a single tribe. The additional similarities between the mature larva of Asteriza and those of Physonota and Cistudinella suggest all three genera should be placed within a single tribe. Key words.— Coleoptera, Chrysomelidae, Cassidinae, Physonotini, Asterizini, Physonota alutacea, Asteriza flavicornis, morphology of immatures, Neotropics. INTRODUCTION Swietojahska and Medeiros -
Coleoptera: Chrysomelidae: Cassidinae: Ischyrosonychini)
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 3227: 34–53 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) Revision of the endemic Hispaniolan genus Asteriza Chevrolat, 1836, with description of two new species (Coleoptera: Chrysomelidae: Cassidinae: Ischyrosonychini) CHULWOO SHIN1,3, CAROLINE S. CHABOO1 & SHAWN M. CLARK2 1Department of Ecology and Evolutionary Biology, Museum of Natural History and Biodiversity Research Institute, 1501 Crestline Drive, Suite #140, Lawrence, Kansas 66049, U. S. A. 2Monte L. Bean Life Science Museum, Brigham Young University, Provo, Utah 84602, U. S. A. 3Corresponding author. E-mail: [email protected] Abstract The cassidine genus Asteriza Chevrolat, 1836 is redescribed and two new species, Asteriza blakeae Shin, Chaboo & Clark and Asteriza tainosa Shin, Chaboo & Clark, are described from the Dominican Republic. A phylogenetic analysis and an illustrated key to the four Asteriza species are provided. Asteriza blakeae is diagnosed by the reddish lateral margin of the pronotum and more swollen brownish elytral margins. Asteriza tainosa is diagnosed by the relatively swollen maxillary and labial palpi and dominant yellow coloration of the elytra and pronotum. Introduction Chevrolat (1836) erected the genus name Asteriza for the Hispaniolan species, Cassida flavicornis Olivier, 1790. He listed two other names, Asteriza punctatissima Klug and Asteriza flavicornis var. retigera Mannerheim, whose origins are unclear since Klug (1829) and Mannerheim (1825) did not include any Asteriza species. Both these two names lack valid records (ICZN 1999, Article 12), and are therefore nomina nuda. -
Sonorensis 2010
Sonorensis contents Sonoran Desert Insects Introduction Arizona-Sonora Desert Museum Our Volume 30, Number 1 Winter 2010 Christine Conte, Ph.D. The Arizona-Sonora Desert Museum Cultural Ecologist, Arizona-Sonora Desert Museum Co-founded in 1952 by 1 Introduction Arthur N. Pack and William H. Carr Craig Ivanyi Christine Conte, Ph.D. photo by Executive Director Alex Wild Christine Conte, Ph.D. The real voyage of discovery consists Cultural Ecologist 2-7 Insects: Six-Legged Arthropods that Run the World not in seeking new landscapes but in having new eyes. Richard C. Brusca, Ph.D. Wendy Moore, Ph.D. & Carl Olson Senior Director, Science and Conservation —Marcel Proust Linda M. Brewer Editing 8-11 Plants & Insects: A 400-Million-Year Co-Evolutionary Dance Wendy Moore, Ph.D ach year, Sonorensis brings the Museum’s It is little wonder that in almost every culture, photo by Alex Wild E Entomology Editor Mark A. Dimmitt, Ph.D. & Richard C. Brusca, Ph.D. conservation science team and its colleagues in throughout world, insects have played a prominent Martina Clary the community to your doorstep with thoughtful, role in philosophy, psychology, and religion. Design and Production engaging, and informative perspectives on the They have been portrayed as symbols of gods and 12-17 Fit to Be Eaten: A Brief Introduction to Entomophagy Sonorensis is published by the Arizona-Sonora Desert natural and cultural history of the Sonoran celebrated in stories, songs, literature, and art. Here Museum, 2021 N. Kinney Road, Tucson, Arizona 85743. Marci Tarre ©2010 by the Arizona-Sonora Desert Museum, Inc. All rights Desert Region. -
A Natural History of Conspecific Aggregations in Terrestrial Arthropods, with Emphasis on Cycloalexy in Leaf Beetles (Coleoptera: Chrysomelidae)
TAR Terrestrial Arthropod Reviews 5 (2012) 289–355 brill.com/tar A natural history of conspecific aggregations in terrestrial arthropods, with emphasis on cycloalexy in leaf beetles (Coleoptera: Chrysomelidae) Jorge A. Santiago-Blay1,*, Pierre Jolivet2,3 and Krishna K. Verma4 1Department of Paleobiology, MRC-121, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, DC 20013-7012, USA 2Natural History Museum, Paris, 67 Boulevard Soult, 75012 Paris, France 3Museum of Entomology, Florida State Collection of Arthropods Gainesville, FL, USA 4HIG 1/327, Housing Board Colony, Borsi, Durg-491001 India *Corresponding author; e-mails: [email protected], [email protected]. PJ: [email protected]; KKV: [email protected] Received on 30 April 2012. Accepted on 17 July 2012. Final version received on 29 October 2012. Summary Aggregations of conspecifics are ubiquitous in the biological world. In arthropods, such aggregations are generated and regulated through complex interactions of chemical and mechanical as well as abiotic and biotic factors. Aggregations are often functionally associated with facilitation of defense, thermomodula- tion, feeding, and reproduction, amongst others. Although the iconic aggregations of locusts, fireflies, and monarch butterflies come to mind, many other groups of arthropods also aggregate. Cycloalexy is a form of circular or quasicircular aggregation found in many animals. In terrestrial arthropods, cycloalexy appears to be a form of defensive aggregation although we cannot rule out other functions, particularly thermomodulation. In insects, cycloalexic-associated behaviors may include coordinated movements, such as the adoption of seemingly threatening postures, regurgitation of presumably toxic compounds, as well as biting movements. These behaviors appear to be associated with attempts to repel objects perceived to be threatening, such as potential predators or parasitoids. -
Hotspots of Mite New Species Discovery: Trombidiformes (2013–2015)
Zootaxa 4208 (1): 001–045 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Editorial ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4208.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:1BEEF6D5-B509-435A-B783-85CFDFEFCB87 Hotspots of mite new species discovery: Trombidiformes (2013–2015) JIAN-FENG LIU1 & ZHI-QIANG ZHANG1,2 1 School of Biological Sciences, the University of Auckland, Auckland, New Zealand 2 Landcare Research, 231 Morrin Road, Auckland, New Zealand; corresponding author: email: [email protected] Abstract This paper reveals the hotspots of new mite discovery through of a survey of type localities of new Trombidiformes spe- cies described in two journals (Systematic & Applied Acarology and Zootaxa) during the last three years (2013–2015). Taxonomically, the 491 new species of the Trombidiformes are highly unevenly distributed among 55 families with top 10 families accounting for over 66% of the total. The Eriophyidae is the top-ranked family. Geographically, these 491 new species are from 55 countries around the world and their distribution among the countries is highly uneven. The majority of these new species (69%) are from the top 10 countries and six of the top ten countries are also megadiversity countries. The top three countries are all from Asia (Iran, China and Malaysia) and they together accounted for over one third of all new species of the Trombidiformes described in the two journals during 2013–2015. Key words: Mites, Trombidiformes, new species, hotspots, type locality, type depository Introduction Discoveries of new species around the world are unevenly distributed; some countries are hotspots for the discovery of new species because they are hotspots of biodiversity (Mittermeier 1988; Gaston 2000) with more undescribed species or a higher concentration of taxonomists (both local and overseas) interested in working on the biodiversity of these regions (or a combination of both). -
Evaluation of Pathways for Exotic Plant Pest Movement Into and Within the Greater Caribbean Region
Evaluation of Pathways for Exotic Plant Pest Movement into and within the Greater Caribbean Region Caribbean Invasive Species Working Group (CISWG) and United States Department of Agriculture (USDA) Center for Plant Health Science and Technology (CPHST) Plant Epidemiology and Risk Analysis Laboratory (PERAL) EVALUATION OF PATHWAYS FOR EXOTIC PLANT PEST MOVEMENT INTO AND WITHIN THE GREATER CARIBBEAN REGION January 9, 2009 Revised August 27, 2009 Caribbean Invasive Species Working Group (CISWG) and Plant Epidemiology and Risk Analysis Laboratory (PERAL) Center for Plant Health Science and Technology (CPHST) United States Department of Agriculture (USDA) ______________________________________________________________________________ Authors: Dr. Heike Meissner (project lead) Andrea Lemay Christie Bertone Kimberly Schwartzburg Dr. Lisa Ferguson Leslie Newton ______________________________________________________________________________ Contact address for all correspondence: Dr. Heike Meissner United States Department of Agriculture Animal and Plant Health Inspection Service Plant Protection and Quarantine Center for Plant Health Science and Technology Plant Epidemiology and Risk Analysis Laboratory 1730 Varsity Drive, Suite 300 Raleigh, NC 27607, USA Phone: (919) 855-7538 E-mail: [email protected] ii Table of Contents Index of Figures and Tables ........................................................................................................... iv Abbreviations and Definitions ..................................................................................................... -
Redalyc.Sesquiterpene Lactone Sequestration by the Tortoise Beetle Physonota Arizonae (Cassidinae)
Journal of the Mexican Chemical Society ISSN: 1870-249X [email protected] Sociedad Química de México México Aregullín, Manuel; Rodríguez, Eloy Sesquiterpene Lactone Sequestration by the Tortoise Beetle Physonota arizonae (Cassidinae) Journal of the Mexican Chemical Society, vol. 47, núm. 2, abril-junio, 2003, pp. 143-145 Sociedad Química de México Distrito Federal, México Available in: http://www.redalyc.org/articulo.oa?id=47547211 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Revista de la Sociedad Química de México, Vol. 47, Núm. 2 (2003) 143-145 Investigación Sesquiterpene Lactone Sequestration by the Tortoise Beetle Physonota arizonae (Cassidinae) Manuel Aregullín and Eloy Rodríguez* Natural Products Laboratory, Biotechnology 259, College of Agriculture and Life Sciences, Cornell University, Ithaca, NY 14853-4301, USA In honor of Dr. Alfonso Romo de Vivar for his contributions to the field of phytochemistry the chemistry of sesquiterpene lactones Recibido el 24 de marzo del 2003; aceptado el 28 de mayo del 2003 Abstract. The phenomenon of sequestration of plant secondary Resumen. El fenómeno de secuestro de metabolitos secundarios de metabolites by herbivorous arthropods and its importance as an plantas por artrópodos hervíboros, y su importancia como estrategia arthropod defense strategy is well