Swallowtail Butterflies (Lepidoptera
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Inside: Idaea Asceta (Prout) (Geometridae), New to the U.S
________________________________________________________________________________________ Volume 53, Number 3 Fall 2011 www.lepsoc.org ________________________________________________________________________________________ Inside: Idaea asceta (Prout) (Geometridae), new to the U.S. Lepidoptera conserva- tion under a changing climate Karl Jordan Award win- ner: Don Lafontaine Life history of Leona’s Little Blue Tiputini Biological Sta- tion, Ecuador Late Season trip to the Richardson Mountains Membership Updates, The Mailbag, Marketplace... ... and more! ________________________________________________________________________________________ ________________________________________________________ Contents ________________________________________________________www.lepsoc.org A Late Season Trip to the Richardson Mountains ____________________________________ Michael Leski. ............................................................................................ 75 Volume 53, Number 3 Report on the Southern Lepidoptersists’ Society and Association Fall 2011 for Tropical Lepidoptera Meeting 2011 The Lepidopterists’ Society is a non-profit ed- Jacqueline Y. Miller. ............................................................................. 78 ucational and scientific organization. The ob- Idaea asceta (Prout) (Geometridae: Sterrhinae) from Texas, new ject of the Society, which was formed in May to the North American fauna 1947 and formally constituted in December Charles V. Covell. ................................................................................... -
A New Macrolepidopteran Moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican Amber
ZooKeys 965: 73–84 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.965.54461 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research A new macrolepidopteran moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican amber Weiting Zhang1,2, Chungkun Shih3,4, YuHong Shih5, Dong Ren3 1 Hebei GEO University, 136 Huaiandonglu, Shijiazhuang 050031, China 2 State Key Laboratory of Pal- aeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, CAS, Nanjing 210008, China 3 College of Life Sciences and Academy for Multidisciplinary Studies, Capital Normal University, 105 Xisan- huanbeilu, Haidian District, Beijing 100048, China 4 Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, USA 5 Laboratorio Dominicano De Ambar Y Gemas, Santo Domingo, Dominican Republic Corresponding author: Weiting Zhang ([email protected]) Academic editor: Gunnar Brehm | Received 19 May 2020 | Accepted 12 August 2020 | Published 3 September 2020 http://zoobank.org/05E273DB-B590-42D1-8234-864A787BE6A0 Citation: Zhang W, Shih C, Shih YH, Ren D (2020) A new macrolepidopteran moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican amber. ZooKeys 965: 73–84. https://doi.org/10.3897/zookeys.965.54461 Abstract A new genus and species of fossil moth, Miogeometrida chunjenshihi Zhang, Shih & Shih, gen. et sp. nov., assigned to Geometridae, is described from Miocene Dominican amber dating from 15–20 Mya. The new genus is characterized by the forewing without a fovea, R1 not anastomosing with Sc, no areole formed by veins R1 and Rs, R1 and Rs1 completely coincident, M2 arising midway between M1 and M3, anal veins 1A and 2A fused for their entire lengths; and the hind wing with Rs running close to Sc + R1 and M2 absent. -
Bionomics of Bagworms (Lepidoptera: Psychidae)
ANRV363-EN54-11 ARI 27 August 2008 20:44 V I E E W R S I E N C N A D V A Bionomics of Bagworms ∗ (Lepidoptera: Psychidae) Marc Rhainds,1 Donald R. Davis,2 and Peter W. Price3 1Department of Entomology, Purdue University, West Lafayette, Indiana, 47901; email: [email protected] 2Department of Entomology, Smithsonian Institution, Washington D.C., 20013-7012; email: [email protected] 3Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona, 86011-5640; email: [email protected] Annu. Rev. Entomol. 2009. 54:209–26 Key Words The Annual Review of Entomology is online at bottom-up effects, flightlessness, mating failure, parthenogeny, ento.annualreviews.org phylogenetic constraint hypothesis, protogyny This article’s doi: 10.1146/annurev.ento.54.110807.090448 Abstract Copyright c 2009 by Annual Reviews. The bagworm family (Lepidoptera: Psychidae) includes approximately All rights reserved 1000 species, all of which complete larval development within a self- 0066-4170/09/0107-0209$20.00 enclosing bag. The family is remarkable in that female aptery occurs in ∗The U.S. Government has the right to retain a over half of the known species and within 9 of the 10 currently recog- nonexclusive, royalty-free license in and to any nized subfamilies. In the more derived subfamilies, several life-history copyright covering this paper. traits are associated with eruptive population dynamics, e.g., neoteny of females, high fecundity, dispersal on silken threads, and high level of polyphagy. Other salient features shared by many species include a short embryonic period, developmental synchrony, sexual segrega- tion of pupation sites, short longevity of adults, male-biased sex ratio, sexual dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case. -
Lepidoptera: Noctuidae) in Washington and Oregon Apple Orchards
HORTICULTURAL ENTOMOLOGY Phenology of Lacanobia subjuncta (Lepidoptera: Noctuidae) in Washington and Oregon Apple Orchards MICHAEL D. DOERR, JAY F. BRUNNER, AND VINCENT P. JONES Washington State University Tree Fruit Research and Extension Center, 1100 N. Western Avenue, Wenatchee, WA 98801 J. Econ. Entomol. 98(6): 2100Ð2106 (2005) ABSTRACT The phenology of Lacanobia subjuncta (Grote & Robinson) (Lepidoptera: Noctuidae) was investigated in 30 apple orchards in central Washington state and northeastern Oregon from 1998 to 2001 (57 total orchard-yr). Adult captures in pheromone-baited traps were Þt to a Weibull distribution to model emergence of the Þrst and second generations. Initial capture of Þrst generation adults was observed at 216.2 Ϯ 2.6 degree-days (DD) (mean Ϯ SEM) from 1 March by using a base temperature of 6.7ЊC. The model predicted that ßight was 5 and 95% complete by 240 and 700 degree-days (DD), respectively. Monitoring of oviposition and hatch was used to establish a protandry plus preoviposition degree-day requirement of 160.0 Ϯ 7.7 DD, as well as to provide data to describe the entire hatch period. Egg hatch was 5 and 95% complete by 395 and 630 DD, respectively. The start of the second ßight was observed at 1217.1 Ϯ 8.3 DD by using an upper threshold for development of 32ЊC and a horizontal cutoff. The model indicated that the second ßight was 5 and 95% complete by 1220 and 1690 DD, respectively. Second generation hatch was 5 and 95% complete by 1440 and 1740 DD, respectively. A discussion of the potential uses of these detailed phenology data in optimizing management strategies is presented. -
Trustees' Annual Report 2019
REPORT OF THE TRUSTEES AND FINANCIAL STATEMENT FOR THE PERIOD 01 JANUARY 2019 TO 31 DECEMBER 2019 Established 04 August 2017 as a Charitable Incorporated Organisation (CIO) Registered Charity Number: 1174142 CONTENTS Charity Information 1 Trustees’ Report 2 Responsibilities 2 Organisation 2 Origins 3 Objectives and Activities 4 Financial Review 6 Reserves 6 Risk Management 6 Plans for the Future Period 7 Statement of Financial Activities 8 Notes to the Financial Statements 9-11 CHARITY INFORMATION Governing Document: CIO Constitution dated 09 May 2017 Charity Number: 1174142 HMRC Charities Reference: EW8083 Registered Address: Swallowtail and Birdwing Butterfly Trust C/o Hines Harvey Woods Queens Head House The Street, Acle Norwich, UK, NR13 7DY Independent Examiner None assigned Accountants: None assigned Solicitors: None assigned Bankers: Barclays Bank PLC, Leicester, LE87 2BB Social Media Advisor: PhaseThree Goods, Norwich Public Relations Advisor: Holdsworth Associates, Cambridge Website: www.sbbt.org.uk Email: [email protected] Telephone: 01493 750207 (registered address only) Facebook: https://www.facebook.com/swallowtailandbirdwing/ 1 TRUSTEES’ REPORT The Swallowtail and Birdwing Butterfly Trust (SBBT) established its Constitution as a Charitable Incorporated Organisation on 09 May 2017 and was entered on the Register of Charities, number 1174142, on 04 August 2017. The Trustees have pleasure in presenting this, their second formal report and financial statement, covering the period 01 January 2019 to 31 December 2019. The financial statement has been prepared in accordance with the document “Accounting and Reporting by Charities: Statement of Recommended Practice, SORP (FRSSE)”, as amended for accounting periods commencing from 1 January 2016. This and future reports will be published on the Charity Commission’s website. -
Impacts of Invasive Alliaria Petiolata on Two Native Pieridae Butterflies, Anthocharis Midea and Pieris Virginiensis
Wright State University CORE Scholar Browse all Theses and Dissertations Theses and Dissertations 2017 Impacts of Invasive Alliaria Petiolata on Two Native Pieridae Butterflies, Anthocharis Midea and Pieris Virginiensis Danielle Marie Thiemann Wright State University Follow this and additional works at: https://corescholar.libraries.wright.edu/etd_all Part of the Biology Commons Repository Citation Thiemann, Danielle Marie, "Impacts of Invasive Alliaria Petiolata on Two Native Pieridae Butterflies, Anthocharis Midea and Pieris Virginiensis" (2017). Browse all Theses and Dissertations. 1849. https://corescholar.libraries.wright.edu/etd_all/1849 This Thesis is brought to you for free and open access by the Theses and Dissertations at CORE Scholar. It has been accepted for inclusion in Browse all Theses and Dissertations by an authorized administrator of CORE Scholar. For more information, please contact [email protected]. IMPACTS OF INVASIVE ALLIARIA PETIOLATA ON TWO NATIVE PERIDAE BUTTERFLIES, ANTHOCHARIS MIDEA AND PIERIS VIRGINIENSIS A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science By DANIELLE MARIE THIEMANN B.S., University of Dayton, 2014 2017 Wright State University WRIGHT STATE UNIVERSITY GRADUATE SCHOOL April 20, 2017 I HEREBY RECOMMEND THAT THE THESIS PREPARED UNDER MY SUPERVISION BY Danielle Marie Thiemann ENTITLED Impacts of Invasive Alliaria petiolata on Two Native Pieridae Butterflies, Anthocharis midea and Pieris virginiensis BE ACCEPTED IN PARTIAL FULFILLMENT OF THE REQUIRMENTS FOR THE DEGREE OF Master of Science. ____________________________________ Donald F. Cipollini, Ph.D. Thesis Director ____________________________________ David L. Goldstein, Ph.D., Chair Department of Biological Sciences Committee on Final Examination ___________________________________ Donald F. Cipollini, Ph.D. -
Lepidoptera: Papilionidae)
Zootaxa 3786 (4): 469–482 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3786.4.5 http://zoobank.org/urn:lsid:zoobank.org:pub:8EC12B47-B992-4B7B-BBF0-BB0344B26BE3 Discovery of a third species of Lamproptera Gray, 1832 (Lepidoptera: Papilionidae) SHAO-JI HU1,5, XIN ZHANG2, ADAM M. COTTON3 & HUI YE4 1Laboratory of Biological Invasion and Ecosecurity, Yunnan University, Kunming, 650091, China. E-mail: [email protected] 2Laboratory for Animal Genetic Diversity and Evolution of Higher Education in Yunnan Province, Yunnan University, Kunming, 650091, China. E-mail: [email protected] 386/2 Moo 5, Tambon Nong Kwai, Hang Dong, Chiang Mai, Thailand. E-mail: [email protected] 4Laboratory Supervisor, Laboratory of Biological Invasion and Ecosecurity, Yunnan University, Kunming, 650091, China. E-mail: [email protected] 5Corresponding author Abstract A newly discovered, third species of the genus Lamproptera (Lepidoptera: Papilionidae) is described, 183 years after the second currently recognised species was first named. Lamproptera paracurius Hu, Zhang & Cotton sp. n., from N.E. Yun- nan, China, is based on marked differences in external morphology and male genital structure. The species is confirmed as a member of the genus, and detailed comparisons are made with other taxa included in the genus. Keys to Lamproptera species based on external characters and male genitalia are included. Key words: Leptocircini, new species, Dongchuan, Yunnan, China Introduction The dragontails, genus Lamproptera Gray, 1832 (Lepidoptera: Papilionidae: Leptocircini), are the smallest papilionid butterflies found in tropical Asia (Tsukada & Nishiyama 1980b). -
Lepidoptera, Noctuidae, Hadeninae) Species of Iran
Turk J Zool 2012; 36(6): 752-758 © TÜBİTAK Research Article doi:10.3906/zoo-1111-15 A survey of the Perigrapha Lederer (Lepidoptera, Noctuidae, Hadeninae) species of Iran Asghar SHIRVANI1,*, Mohammad Ali SHOGHALI2, Shamsi FEIZPOOR3 1Department of Plant Protection, Faculty of Agriculture, Shahid Bahonar University of Kerman, 76169-133 Kerman – IRAN 2No. 51, 24 Azar Street, Kerman – IRAN 3Young Researchers Society, Shahid Bahonar University of Kerman, Kerman – IRAN Received: 14.11.2011 ● Accepted: 25.03.2012 Abstract: Four species of the genus Perigrapha Lederer are reviewed in Iran. Two species, P. annau Varga & Ronkay, 1991 and P. fl ora Hreblay, 1996, are reported for the fi rst time from the fauna of Iran. Adult and genitalia images are illustrated and identifi cation keys for the external and genital features are given. Key words: Perigrapha, Iran, new records, identifi cation key Introduction large-scale variation in morphological features and Th e tribe Orthosiini Guenée, 1837, with 7 genera relegated them as members of 3 genera, Anorthoa, (Panolis Hübner, [1821], Dioszeghyana Hreblay, Harutaeographa, and Perigrapha. 1993, Orthosia Ochsenheimer, 1816, Anorthoa Berio, Perigrapha, a Holarctic genus belonging to the 1980, Harutaeographa Yoshimoto, 1993, Perigrapha perigraphoid generic complex with hairy eyes typical Lederer, 1857, and Egira Duponchel, 1845), is for the subfamily Hadeninae (sensu Hampson), represented by early-fl ying, univoltine species that comprises 3 subgenera, Opacographa Hreblay, 1996, prefer mountainous and semimountainous regions Rororthosia Beck, 1999, and Perigrapha Lederer, in Iran. Th e classifi cation and taxonomic rank of 1857. Th is genus is represented in Europe by the species groups within this tribe has been a matter last 2 subgenera and 4 species (Ronkay et al., 2001). -
Phylogeny and Evolution of Lepidoptera
EN62CH15-Mitter ARI 5 November 2016 12:1 I Review in Advance first posted online V E W E on November 16, 2016. (Changes may R S still occur before final publication online and in print.) I E N C N A D V A Phylogeny and Evolution of Lepidoptera Charles Mitter,1,∗ Donald R. Davis,2 and Michael P. Cummings3 1Department of Entomology, University of Maryland, College Park, Maryland 20742; email: [email protected] 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560 3Laboratory of Molecular Evolution, Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland 20742 Annu. Rev. Entomol. 2017. 62:265–83 Keywords Annu. Rev. Entomol. 2017.62. Downloaded from www.annualreviews.org The Annual Review of Entomology is online at Hexapoda, insect, systematics, classification, butterfly, moth, molecular ento.annualreviews.org systematics This article’s doi: Access provided by University of Maryland - College Park on 11/20/16. For personal use only. 10.1146/annurev-ento-031616-035125 Abstract Copyright c 2017 by Annual Reviews. Until recently, deep-level phylogeny in Lepidoptera, the largest single ra- All rights reserved diation of plant-feeding insects, was very poorly understood. Over the past ∗ Corresponding author two decades, building on a preceding era of morphological cladistic stud- ies, molecular data have yielded robust initial estimates of relationships both within and among the ∼43 superfamilies, with unsolved problems now yield- ing to much larger data sets from high-throughput sequencing. Here we summarize progress on lepidopteran phylogeny since 1975, emphasizing the superfamily level, and discuss some resulting advances in our understanding of lepidopteran evolution. -
Insect Declines in the Anthropocene
EN65CH23_Wagner ARjats.cls December 19, 2019 12:24 Annual Review of Entomology Insect Declines in the Anthropocene David L. Wagner Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, Connecticut 06269, USA; email: [email protected] Annu. Rev. Entomol. 2020. 65:457–80 Keywords First published as a Review in Advance on insect decline, agricultural intensi!cation, climate change, drought, October 14, 2019 precipitation extremes, bees, pollinator decline, vertebrate insectivores The Annual Review of Entomology is online at ento.annualreviews.org Abstract https://doi.org/10.1146/annurev-ento-011019- Insect declines are being reported worldwide for "ying, ground, and aquatic 025151 lineages. Most reports come from western and northern Europe, where the Copyright © 2020 by Annual Reviews. insect fauna is well-studied and there are considerable demographic data for All rights reserved many taxonomically disparate lineages. Additional cases of faunal losses have been noted from Asia, North America, the Arctic, the Neotropics, and else- where. While this review addresses both species loss and population declines, its emphasis is on the latter. Declines of abundant species can be especially worrisome, given that they anchor trophic interactions and shoulder many Access provided by 73.198.242.105 on 01/29/20. For personal use only. of the essential ecosystem services of their respective communities. A review of the factors believed to be responsible for observed collapses and those Annu. Rev. Entomol. 2020.65:457-480. Downloaded from www.annualreviews.org perceived to be especially threatening to insects form the core of this treat- ment. In addition to widely recognized threats to insect biodiversity, e.g., habitat destruction, agricultural intensi!cation (including pesticide use), cli- mate change, and invasive species, this assessment highlights a few less com- monly considered factors such as atmospheric nitri!cation from the burning of fossil fuels and the effects of droughts and changing precipitation patterns. -
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. -
Whole Genome Shotgun Phylogenomics Resolves the Pattern
Whole genome shotgun phylogenomics resolves the pattern and timing of swallowtail butterfly evolution Rémi Allio, Celine Scornavacca, Benoit Nabholz, Anne-Laure Clamens, Felix Sperling, Fabien Condamine To cite this version: Rémi Allio, Celine Scornavacca, Benoit Nabholz, Anne-Laure Clamens, Felix Sperling, et al.. Whole genome shotgun phylogenomics resolves the pattern and timing of swallowtail butterfly evolution. Systematic Biology, Oxford University Press (OUP), 2020, 69 (1), pp.38-60. 10.1093/sysbio/syz030. hal-02125214 HAL Id: hal-02125214 https://hal.archives-ouvertes.fr/hal-02125214 Submitted on 10 May 2019 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. Running head Shotgun phylogenomics and molecular dating Title proposal Downloaded from https://academic.oup.com/sysbio/advance-article-abstract/doi/10.1093/sysbio/syz030/5486398 by guest on 07 May 2019 Whole genome shotgun phylogenomics resolves the pattern and timing of swallowtail butterfly evolution Authors Rémi Allio1*, Céline Scornavacca1,2, Benoit Nabholz1, Anne-Laure Clamens3,4, Felix