Redalyc.Plants and Butterflies of a Small Urban Preserve in the Central
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Amphiesmeno- Ptera: the Caddisflies and Lepidoptera
CY501-C13[548-606].qxd 2/16/05 12:17 AM Page 548 quark11 27B:CY501:Chapters:Chapter-13: 13Amphiesmeno-Amphiesmenoptera: The ptera:Caddisflies The and Lepidoptera With very few exceptions the life histories of the orders Tri- from Old English traveling cadice men, who pinned bits of choptera (caddisflies)Caddisflies and Lepidoptera (moths and butter- cloth to their and coats to advertise their fabrics. A few species flies) are extremely different; the former have aquatic larvae, actually have terrestrial larvae, but even these are relegated to and the latter nearly always have terrestrial, plant-feeding wet leaf litter, so many defining features of the order concern caterpillars. Nonetheless, the close relationship of these two larval adaptations for an almost wholly aquatic lifestyle (Wig- orders hasLepidoptera essentially never been disputed and is supported gins, 1977, 1996). For example, larvae are apneustic (without by strong morphological (Kristensen, 1975, 1991), molecular spiracles) and respire through a thin, permeable cuticle, (Wheeler et al., 2001; Whiting, 2002), and paleontological evi- some of which have filamentous abdominal gills that are sim- dence. Synapomorphies linking these two orders include het- ple or intricately branched (Figure 13.3). Antennae and the erogametic females; a pair of glands on sternite V (found in tentorium of larvae are reduced, though functional signifi- Trichoptera and in basal moths); dense, long setae on the cance of these features is unknown. Larvae do not have pro- wing membrane (which are modified into scales in Lepi- legs on most abdominal segments, save for a pair of anal pro- doptera); forewing with the anal veins looping up to form a legs that have sclerotized hooks for anchoring the larva in its double “Y” configuration; larva with a fused hypopharynx case. -
Entomopatogen Nematode Exploration and Virulency Against Spodoptera Frugiperda J.E Smith
Content available at : https://ejournal.unib.ac.id/index.php/jagritropica/index ISSN (PRINT) 2621-217X ISSN (ONLINE) 2621-699X Entomopatogen nematode exploration and virulency against Spodoptera frugiperda J.E Smith Winda Septi Hade1, Djamilah1*, Priyatiningsih 1 Departement of Plant Protection, Faculty of Agriculture, Universitas Bengkulu, Kandang Limun, Bengkulu, Indonesia *Corresponding author: [email protected] ABSTRACT : Corn (Zea mays L) is a very important food and animal feed after rice. One of the important pests that attack corn plants is Spodoptera frugiperda J.E Smith. This pest is a new pest and is a major pest in corn. In pest control, farmers generally use synthetic chemicals. In an effort to reduce these negative impacts synthetic chemical, entomopathogenic nematode (NEP) was chosen as one of the more environmentally friendly control techniques. This study aims to obtain NEP isolates, population density and virulence against S. frugiperda. This research was conducted at the Plant Protection Laboratory, Bengkulu University from December 2019 to April 2020. This study used a Factorial Completely Randomized Design (CRD) with 4 treatments and 5 replications. The treatments consisted of NEP concentrations : 0 Jl / ml; 200 Jl / 1ml; 400 Jl / 2ml; 600 Jl / 3ml originating from Bengkulu and Kepahiang isolates. Each experiment consisted of 3 S. frugiperda larvae. The results showed that the NEP obtained from each region, namely the genus Steinermatidae. Population density of 9,005 NEP / 5ml in the Kepahiang area and 6,837 NEP / 5ml in the Bengkulu region. NEP virulence test against S. frugiperda larvae showed that 200 Jl / ml concentration was able to control S. -
2012 Edmonton, Alberta
October 2013 ISSN 0071-0709 PROCEEDINGS OF THE 60TH ANNUAL MEETING OF THE Entomological Society of Alberta November 4th-7th 2012 Edmonton, Alberta Entomological Society of Alberta Board of Directors 2012 ....................................... 5 Annual Meeting Committees 2012 ..................................................................................... 5 Program of the 60th Annual Meeting of the Entomological Society of Alberta .... 6 Oral Presentations ................................................................................................................ 12 Poster Presentations ............................................................................................................ 26 Index to Authors..................................................................................................................... 29 Minutes of the Entomological Society of Alberta Executive Meeting .................. 40 DRAFT Minutes of the Entomological Society of Alberta 60th Annual AGM ...... 42 Regional Director’s Report ................................................................................................. 45 Northern Director’s Report ................................................................................................ 47 Central Director’s Report .................................................................................................... 51 Southern Director’s Report ................................................................................................ 53 Webmaster’s Report ............................................................................................................ -
Ecological Divergence and Speciation in Heliconius Cydno and H
Ecological divergence and speciation in Heliconius cydno and H. melpomene by Russell Edward Naisbit A thesis submitted for the degree of Doctor of Philosophy of the University of London September 2001 Department of Biology University College London To my family, for their support and encouragement throughout this crazy endeavour 2 “It is hardly an exaggeration to say, that whilst reading and reflecting on the various facts given in this Memoir, we feel to be as near witnesses, as we can ever hope to be, of the creation of a new species on this earth.” Charles Darwin, Natural History Review: Quarterly Journal of Biological Science, 1863. From a review of “Contributions to an Insect Fauna of the Amazon Valley,” in which Henry Walter Bates gave an adaptive explanation for mimicry in Amazonian butterflies and argued that variation in mimicry might cause speciation 3 Abstract We are in the midst of a renaissance in speciation research. There is a return to Darwin’s belief in the role of natural selection in driving speciation, after a lengthy focus on geographic isolation and hybrid sterility. Here I describe the ecological, behavioural, and genetic bases of speciation in Heliconius cydno and Heliconius melpomene (Lepidoptera: Nymphalidae). The two species are sympatric in tropical rainforest across most of Central America and the foothills of the Andes. Ecological differentiation allows coexistence of these sister species despite rare hybridisation. Divergence in microhabitat and larval host plant use has reduced both the potential for gene flow and for competition. In Panama H. cydno uses most Passiflora species in closed canopy forest, whilst H. -
The Utilization of Insects As a Sustainable and Secure Source of Animal-Based Food for the Human Diet Has Continued to Incr
Geo-Eco-Trop, 2016, 40-2, n.s.: 145-174 Preliminary knowledge for breeding edible caterpillars in Congo-Brazzaville Connaissances préliminaires pour l’élevage de chenilles comestibles au Congo-Brazzaville Germain MABOSSY-MOBOUNA1, Thierry BOUYER2, Paul LATHAM3, Paulette ROULON- DOKO4, Augustin KONDA KU MBUTA5, François MALAISSE6,7 Résumé: La consommation humaine de Lépidoptères est un thème à la mode. Si une information de base est à présent disponible concernant la diversité des chenilles consommées en République du Congo-Brazzaville, nous ne disposons pas de données préliminaires solides concernant leur distribution, la littérature qui leur a été consacrées, leur saisonnalité et leur cycle de vie, leurs dénominations locales et leurs plantes hôtes. C’est l’objet du présent article, qui en outre permet de dégager les domaines qui nécessitent des études plus approfondies. Vingt taxons sont pris en considération, dont seize identifiés au niveau de l’espèce. Seuls deux cycles de vie sont à présent connus. Quatre-vingt-neuf noms vernaculaires sont cités. Ces chenilles se nourrissent d’au moins 40 plantes hôtes qui sont citées ainsi que des sources de documentation concernant ces dernières. Mots-clés : Congo-Brazzaville, Lépidoptères, chenilles consommées, distribution, dénominations vernaculaires, plantes hôtes, cycle de vie, valeurs alimentaires. Abstract: Human consumption of Lepidoptera is a subject of current interest. Though basic information is presently available regarding the diversity of caterpillars eaten in Congo-Brazzaville, no robust data regarding their distribution, reference material, seasonality and life cycle, local names and host-plants is available. The purpose of this article, which also identifies areas that require further study, is to address this gap. -
Eremonidiopsis Aggregata, Gen. N., Sp. N. from Cuba, the Third West Indian Dioptinae (Lepidoptera, Notodontidae)
A peer-reviewed open-access journal ZooKeys Eremonidiopsis333: 77–91 (2013) aggregata, gen. n., sp. n. from Cuba, the third West Indian Dioptinae... 77 doi: 10.3897/zookeys.333.5483 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research Eremonidiopsis aggregata, gen. n., sp. n. from Cuba, the third West Indian Dioptinae (Lepidoptera, Notodontidae) Rayner Núñez Aguila1,† 1 División de Colecciones Zoológicas y Sistemática, Instituto de Ecología y Sistemática, Carretera de Varona km 3. 5, Capdevila, Boyeros, La Habana, Cuba. CP 11900. Habana 19 † http://zoobank.org/C305E384-2206-4258-B49D-3D9C7CB60D98 Corresponding author: Rayner Núñez Aguila ([email protected], [email protected]) Academic editor: Donald Lafontaine | Received 8 May 2013 | Accepted 30 July 2013 | Published 20 September 2013 http://zoobank.org/76AFA50B-94CB-48DD-88FA-D7EB09CF9C71 Citation: Aguila RN (2013) Eremonidiopsis aggregata, gen. n., sp. n. from Cuba, the third West Indian Dioptinae (Lepidoptera, Notodontidae). ZooKeys 333: 77–91. doi: 10.3897/zookeys.333.5483 Abstract A new genus and species of Dioptinae (Lepidoptera, Noctuoidea, Notodontidae) is described from Cuba, this being the third taxon of the subfamily known from the West Indies. Eremonidiopsis aggregata, gen. n., sp. n., appears to be closely related to Eremonidia mirifica Rawlins & Miller from Hispaniola among members of the tribe Dioptini. Eremonidiopsis aggregata is known from two localities in the middle and western portions of the northeastern Cuban mountain range, Nipe–Sagua–Baracoa. The species inhabits low elevations (300–400 m) covered by lowland rainforest and sclerophyll rainforest. The six known specimens, all males, were part of small swarms flying near the top of an unidentified tree during the day at both collecting sites. -
Trichoptera)" (2018)
Clemson University TigerPrints All Theses Theses 5-2018 Description and Diagnosis of Associated Larvae and Adults of Vietnamese and South Carolina Caddisflies T( richoptera) Madeline Sage Genco Clemson University, [email protected] Follow this and additional works at: https://tigerprints.clemson.edu/all_theses Recommended Citation Genco, Madeline Sage, "Description and Diagnosis of Associated Larvae and Adults of Vietnamese and South Carolina Caddisflies (Trichoptera)" (2018). All Theses. 2839. https://tigerprints.clemson.edu/all_theses/2839 This Thesis is brought to you for free and open access by the Theses at TigerPrints. It has been accepted for inclusion in All Theses by an authorized administrator of TigerPrints. For more information, please contact [email protected]. DESCRIPTION AND DIAGNOSIS OF ASSOCIATED LARVAE AND ADULTS OF VIETNAMESE AND SOUTH CAROLINA CADDISFLIES (TRICHOPTERA) A Thesis Presented to the Graduate School of Clemson University In Partial Fulfillment of the Requirements for the Degree Master of Science Entomology by Madeline Sage Genco May 2018 Accepted by: Dr. John C. Morse, Committee Co-chair Dr. Michael Caterino, Committee Co-chair Dr. Kyle Barrett ABSTRACT Globally, only 868 trichopteran larvae have been described to enable species-level identification; that is only 0.05% of all caddisfly species. In the Oriental Region, almost none (0.016%) of the larvae are known. Continued work on describing larval species may improve the accuracy of water quality monitoring metrics. Genetic barcoding (with mtCOI) was used to associate unknown larvae with known or unknown adults. The morphology of the larvae was then described in words as well as in illustrations to aid species-level identification. -
Bulletin Letin Bull
BULLETINBULLETIN ¥™ ™ A REVIEWA REVIEW OF OF VIRBIA VIRBIA (FORMERLY (FORMERLY HOLOMELINA HOLOMELINA) OF) OF AMERICA AMERICA NORTHNORTH OF OF MEXICO MEXICO (ARCTIIDAE: (ARCTIIDAE: ARCTIINAE: ARCTIINAE: ARCTIINI) ARCTIINI) J. M.J. M.Zaspel, Zaspel, S. J. S. Weller, J. Weller, and and R.T. R.T. Cardé Cardé Vol. Vol. 48, No.48, No.3, pp. 2, pp.59-118 59-118 2008 2008 UNIVERSITYUNIVERSITY OF OFFLORIDA FLORIDA GAINESVILLE GAINESVILLE ZASPEL, WELLER and CARDÉ : Virbia of America north of Mexico 119 The FLORIDA MUSEUM OF NATURAL HISTORY is Florida’s state museum of natural history, dedicated to understanding, preserving, and interpreting biological diversity and cultural heritage. The BULLETIN OF THE FLORIDA MUSEUM OF NATURAL HISTORY is a peer-reviewed publication that publishes the results of original research in zoology, botany, paleontology, and archaeology. Address all inquiries to the Managing Editor of the Bulletin. Numbers of the Bulletin are published at irregular intervals. Specific volumes are not necessarily completed in any one year. The end of a volume will be noted at the foot of the first page of the last issue in that volume. Richard Franz, Managing Editor Cathleen Bester, Production Bulletin Committee Richard Franz, Chairperson Ann Cordell Sarah Fazenbaker Richard Hulbert William Marquardt Larry Page Irvy R. Quitmyer David W. Steadman, Ex officio Member ISSN: 0071-6154 Publication Date: December 30, 2008 Send communications concerning purchase or exchange of the publication and manuscript queries to: Managing Editor of the BULLETIN Florida Museum of Natural History University of Florida PO Box 117800 Gainesville, FL 32611-7800 U.S.A. Phone: 352-392-1721 Fax: 352-846-0287 e-mail: [email protected] ZASPEL, WELLER and CARDÉ : Virbia of America north of Mexico 59 A REVIEW OF VIRBIA (FORMERLY HOLOMELINA) OF AMERICA NORTH OF MEXICO (ARCTIIDAE: ARCTIINAE: ARCTIINI) J. -
Lepidoptera: Crambidae): a Flower Bud-Feeder on PAssiflora Mollissima, an Invasive Vine in HaWaiian Forests Mohsen M
RAMADAN et al.: Field biology of Pyrausta perelegans TROP. LEPID. RES., 18(2):113-121, 2008 113 FIELD BIOLOGY OF PYRAUS TA PERELEGANS (LEPIDOPTERA: CRAMBIDAE): A FLOWER BUD-FEEDER ON P ASSIFLORA MOLLISSIMA, AN INVASIVE VINE IN HA WAIIAN FORESTS Mohsen M. Ramadan¹, George P. Markin², and Marshall W. Johnson Department of Plant and Environmental Sciences, University of Hawaii, 3050 Maile Way, Honolulu, Hawaii 96822 Abstract - This study is a continuation of efforts to monitor a population of the biological control agent, Pyrausta perelegans Hampson (Lepidoptera: Crambidae), which specializes on the flower buds of the forest invasive vinePassiflora mollissima (H.B.K.) Bailey. Post-establishment studies were conducted to evaluate the effect of P. perelegans and factors affecting its colonization potential shortly after its establishment in the Olaa rain forest, Hawaii Volcanoes National Park (1800 m elevation), island of Hawaii. Moth population growth was monitored over a period of 16 months using a UV light trap. The moth appeared during months of 1992-1993, with a maximum population build-up during May (0.67 moth/night) and October (0.6 moth/night) of 1992. In March and May of 1993 the moth population peaked at an average of 0.4 moth/night. Mean moth catch per night during the two years was not significantly different. Overall mean percentage of vines infested with eggs of P. perelegans was 5.5% with a mean of 4.7 eggs per vine. Most of the eggs (75%) were deposited on the underside of young leaves with midrib lengths ranging from 2.5 to 6.5 cm. -
Tiger Moth Responses to a Simulated Bat Attack: Timing and Duty Cycle J
2637 The Journal of Experimental Biology 209, 2637-2650 Published by The Company of Biologists 2006 doi:10.1242/jeb.02295 Tiger moth responses to a simulated bat attack: timing and duty cycle J. R. Barber* and W. E. Conner Department of Biology, Wake Forest University, 226 Winston Hall, Winston-Salem, NC 27109, USA *Author for correspondence (e-mail: [email protected]) Accepted 24 April 2006 Summary Many night-flying insects perform complex, aerobatic The assemblage reached a half-maximum response shortly escape maneuvers when echolocating bats initiate attack. after the first response, at 763±479·ms from the end of the Tiger moths couple this kinematic defense with an terminal buzz. Tiger moth response reached a maximum acoustic reply to a bat’s biosonar-guided assault. The at 475±344·ms from the end of the sequence; during the jamming hypothesis for the function of these moth sounds approach phase, well before the onset of the terminal assumes that tiger moth clicks presented at high densities, buzz. In short, much of tiger moth response to bat attack temporally locked to the terminal phase of the bat attack occurs outside of the jamming hypotheses’ predictions. will produce the greatest jamming efficacy. Furthermore, no relationship exists between the duty cycle Concomitantly, this hypothesis argues that moths warning of a tiger moth’s call (and thus the call’s probability of bats of bad tasting chemicals sequestered in their tissues jamming the bat) and its temporal response to bat attack. should call early to give the bat time to process the These data call into doubt the assumptions behind the meaning of the warning signal and that moths calling at jamming hypothesis as currently stated but do not directly low duty cycles are more likely to employ such an test the functionality of arctiid sounds in disrupting aposematic strategy. -
IMMATURE STAGES of VENEZUELAN DIOPTINAE (NOTODONTIDAE) in Josia and THIRMIDA
Journal of the Lepidopterists' Society 48(4), 1994,338- 372 IMMATURE STAGES OF VENEZUELAN DIOPTINAE (NOTODONTIDAE) IN jOSIA AND THIRMIDA JAMES S. MILLER Department of Entomology, American Museum of Natural History, Central Park West at 79th Street, New York, New York 10024, USA AND L. DANIEL OTERO Laboratorio de Quimica Ecol6gica, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, La Hechicera, Merida 5101, Venezuela ABSTRACT. Immature stages of five species of Dioptinae (Notodontidae) from Ven ezuela are described and illustrated. Four are in the genus .Josia HLibner and one is in Thirmida Walker. All feed as larvae on Passijlora (Passi£loraceae). This is the first life history reported for a member of Thirmida. Immature stages are described for each species, and distributional and host plant data are provided. The tribe Josiini, formerly a subfamily (Josiinae), is delineated. It comprises 103 species in eleven dioptine genera. josia turgida and Thirmida discinota, treated by previous authors as subspecies, are revised to species status. Additional key words: Josiini, Passijlora, montane forest, larval morphology. The Neotropical moth subfamily Dioptinae is unique among Noto dontidae in containing many diurnal forms with aposematic color pat terns (Hering 1925, Kohler 1930, Miller 1992a). The group includes over 400 described species (Byrk 1930), most of which are poorly rep resented in museums worldwide. The most commonly collected diop tines are those in josia, a genus distributed from southern Mexico south to northern Argentina. josia adults are strikingly colored, usually with orange or yellow markings against a dark ground color, and they tend to fly in a slow, fluttering manner. -
INDEX for VOLUME 53 (New Names in Boldface)
Juurnal of the Lepidopterists' Society 5.3(4),1999,173-176 INDEX FOR VOLUME 53 (new names in boldface) Abies, 26 Asia, 7 oberthurii aberthurii, 148 Accuminulia,60 Attacini, 50, 133 oileus, 148 buscki,60 Attacus oileus scamander, 148 longiphallus,60 atlas, 134 placidianus, 14k Achillea Australia, 1 praxsiodus, 148 lanulosa, 74 prometheus epirnetheus, 148 millefolium , 74 Balcazar-Lara, M. A., 45 teucer, 148 Actias Basilarchia Callophrys selene, 134 archippus archippus, 1.04 xami, 170 luna, 134 arthemis astyanax, 104 Callosamia, 22, 49 Adamski, D., 29 arthemis arthemis, 104 angulifem, 26, 134 Aglossa,8 Berenbaum, M., 104 promethea, SO, 134 capemlis, 2 Bicyelus, 26 securifera, 26, 134 Agmulis, 17 Bidens pilosa, 15 Calvert, W. H., 37 Aiello, 142 bi ennialism, 127 Cammisonia, 171 Alberta, Canada, 127 biodiversity, 65, 153 bistorta, 172 Albu, V , 45 bird dropping, 104 strigulosa, 172 allelochcmicals, 104 Biston Carceiia alpine habitat, 32 betularia, 99 reelinata, 72 Arnathes betularia cognataria, 101 catchability, 138 glareosa, 99 black swallowtail, 104 caterpillar, 22 Amazonia, 65 Blastobasinac, 29 Catoblepia Anopheles, 106 Blastobasini, 29 amphirhoe, 148 Anthemea, 134 Blepolenis orgetorix championi, 148 hartii, 134 batea,146 Cotoemsis,8 pemyi, 134 Bolivia, 65 Ceanothus polyphemus, 134 Bolaria integurri'mus) 22 antioxidant, 104 acrocnema, 32 Ceanothus silk moth, 22 anti-predation, 130 improba, 32 Celtis, 130 apricot, 60 Brassolinae, 142 censusing, 13R Arbutus Brassolis Central Am erica, 142 menziesii, 22 astyra, 142 Cephise,77 xalapensis, 27 astyra astyra, 142 nuspesez, 77 Archipini, 114 isthmia, 142 Chao, 65 Arctiidae, 72 sophome,142 Chiapas, Mexico, 153, 155 Arctonotus Brazil, 11 , 65, lOR Chile, 60 lucidus, 171 British Columbia, 22, 74 Chileulia, 64 Arctostaphylos Brown, J.