249 Performance of a Butterfly in Take-Off Flight
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The Complete Mitochondrial Genome of the Fall Webworm, Hyphantria
Int. J. Biol. Sci. 2010, 6 172 International Journal of Biological Sciences 2010; 6(2):172-186 © Ivyspring International Publisher. All rights reserved Research Paper The complete mitochondrial genome of the fall webworm, Hyphantria cunea (Lepidoptera: Arctiidae) Fang Liao1,2, Lin Wang3, Song Wu4, Yu-Ping Li4, Lei Zhao1, Guo-Ming Huang2, Chun-Jing Niu2, Yan-Qun Liu4, , Ming-Gang Li1, 1. College of Life Sciences, Nankai University, Tianjin 300071, China 2. Tianjin Entry-Exit Inspection and Quarantine Bureau, Tianjin 300457, China 3. Beijing Entry-Exit Inspection and Quarantine Bureau, Beijing 101113, China 4. College of Bioscience and Biotechnology, Shenyang Agricultural University, Liaoning, Shenyang 110866, China Corresponding author: Y. Q. Liu, College of Bioscience and Biotechnology, Shenyang Agricultural University, Liaoning, Shenyang 110866, China; Tel: 86-24-88487163; E-mail: [email protected]. Or to: M. G. Li, College of Life Sciences, Nankai University, Tianjin 300071, China; Tel: 86-22-23508237; E-mail: [email protected]. Received: 2010.02.03; Accepted: 2010.03.26; Published: 2010.03.29 Abstract The complete mitochondrial genome (mitogenome) of the fall webworm, Hyphantria cunea (Lepidoptera: Arctiidae) was determined. The genome is a circular molecule 15 481 bp long. It presents a typical gene organization and order for completely sequenced lepidopteran mitogenomes, but differs from the insect ancestral type for the placement of tRNAMet. The nucleotide composition of the genome is also highly A + T biased, accounting for 80.38%, with a slightly positive AT skewness (0.010), indicating the occurrence of more As than Ts, as found in the Noctuoidea species. All protein-coding genes (PCGs) are initiated by ATN codons, except for COI, which is tentatively designated by the CGA codon as observed in other le- pidopterans. -
The Endangered Butterfly Charonias Theano (Boisduval)(Lepidoptera
Neotropical Entomology ISSN: 1519-566X journal homepage: www.scielo.br/ne ECOLOGY, BEHAVIOR AND BIONOMICS The Endangered Butterfly Charonias theano (Boisduval) (Lepidoptera: Pieridae): Current Status, Threats and its Rediscovery in the State of São Paulo, Southeastern Brazil AVL Freitas1, LA Kaminski1, CA Iserhard1, EP Barbosa1, OJ Marini Filho2 1 Depto de Biologia Animal & Museu de Zoologia, Instituto de Biologia, Univ Estadual de Campinas, Campinas, SP, Brasil 2Centro de Pesquisa e Conservação do Cerrado e Caatinga – CECAT, Instituto Chico Mendes de Conservação da Biodiversidade, Brasília, DF, Brasil Keywords Abstract Aporiina, Atlantic Forest, endangered species, Pierini, Serra do Japi The pierid Charonias theano Correspondence (Boisduval), an endangered butterfly André V L Freitas, Depto de Biologia Animal & species, has been rarely observed in nature, and has not been recorded Museu de Zoologia, Instituto de Biologia, Univ in the state of CSão. theano Paulo in the last 50 years despite numerous efforts Estadual de Campinas, CP6109, 13083-970, Campinas, SP, Brasil; [email protected] to locate extant colonies. Based on museum specimens and personal information, was known from 26 sites in southeastern Edited by Kleber Del Claro – UFU and southern Brazil. Recently, an apparently viable population was recorded in a new locality, at Serra do Japi, Jundiaí, São Paulo, with Received 26 May 2011 and accepted 03 severalsince this individuals site represents observed one of during the few two large weeks forested in April, protected 2011. areas The August 2011 existence of this population at Serra do Japi is an important finding, São Paulo, but within its entire historical distribution. where the species could potentially persist not only in the state of Introduction In the last Brazilian red list of endangered fauna (Machado intensively sampled from 1987 to 1991, resulting in a list et al of 652 species (Brown 1992). -
Logistic Regression Is a Better Method of Analysis Than
Scientific Notes 1183 LOGISTIC REGRESSION IS A BETTER METHOD OF ANALYSIS THAN LINEAR REGRESSION OF ARCSINE SQUARE ROOT TRANSFORMED PROPORTIONAL DIAPAUSE DATA OF PIERIS MELETE (LEPIDOPTERA: PIERIDAE) 1 2 3, P. J. SHI , H. S. SANDHU AND H. J. XIAO * 1Key Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China 2University of Florida, Institute of Food and Agricultural Sciences, Everglades Research and Education Center, Belle Glade, FL, USA 3Institute of Entomology, Jiangxi Agricultural University, Nanchang 330045, China *Corresponding author; E-mail: [email protected] Recently, Xiao et al. (2012) published a study the response variable are linear. However, non- on the effects of daily average temperature and linear effects are ubiquitous in nature. Therefore, natural day-length on the incidence of summer linear regression actually neglected the non- and winter diapause in the Cabbage Butterfly, linear effects, which led to low goodness-of-fit to Pieris melete Ménétriés (Lepidoptera: Pieridae). the objective data. Additionally, the proportional Under field conditions, the cabbage butterfly, data were arcsine square root transformed before Pieris melete, displays a pupal summer diapause performing the linear regression. Although this in response to relatively low daily temperatures transformation has long been standard procedure and gradually increasing day-length during in analyzing proportional data in ecology, logistic spring, and a pupal winter diapause in response regression has greater interpretability and high- to the progressively shorter day-length. To de- er power than transformation in data containing termine whether photoperiod has a stronger role binomial and non-binomial response variables than temperature in the determination of the (Warton & Hui 2011). -
BUTTERFLIES in Thewest Indies of the Caribbean
PO Box 9021, Wilmington, DE 19809, USA E-mail: [email protected]@focusonnature.com Phone: Toll-free in USA 1-888-721-3555 oror 302/529-1876302/529-1876 BUTTERFLIES and MOTHS in the West Indies of the Caribbean in Antigua and Barbuda the Bahamas Barbados the Cayman Islands Cuba Dominica the Dominican Republic Guadeloupe Jamaica Montserrat Puerto Rico Saint Lucia Saint Vincent the Virgin Islands and the ABC islands of Aruba, Bonaire, and Curacao Butterflies in the Caribbean exclusively in Trinidad & Tobago are not in this list. Focus On Nature Tours in the Caribbean have been in: January, February, March, April, May, July, and December. Upper right photo: a HISPANIOLAN KING, Anetia jaegeri, photographed during the FONT tour in the Dominican Republic in February 2012. The genus is nearly entirely in West Indian islands, the species is nearly restricted to Hispaniola. This list of Butterflies of the West Indies compiled by Armas Hill Among the butterfly groupings in this list, links to: Swallowtails: family PAPILIONIDAE with the genera: Battus, Papilio, Parides Whites, Yellows, Sulphurs: family PIERIDAE Mimic-whites: subfamily DISMORPHIINAE with the genus: Dismorphia Subfamily PIERINAE withwith thethe genera:genera: Ascia,Ascia, Ganyra,Ganyra, Glutophrissa,Glutophrissa, MeleteMelete Subfamily COLIADINAE with the genera: Abaeis, Anteos, Aphrissa, Eurema, Kricogonia, Nathalis, Phoebis, Pyrisitia, Zerene Gossamer Wings: family LYCAENIDAE Hairstreaks: subfamily THECLINAE with the genera: Allosmaitia, Calycopis, Chlorostrymon, Cyanophrys, -
An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
© Copyright Australian Museum, 2005 Records of the Australian Museum (2005) Vol. 57: 375–446. ISSN 0067-1975 An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna M.S. MOULDS Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] ABSTRACT. The history of cicada family classification is reviewed and the current status of all previously proposed families and subfamilies summarized. All tribal rankings associated with the Australian fauna are similarly documented. A cladistic analysis of generic relationships has been used to test the validity of currently held views on family and subfamily groupings. The analysis has been based upon an exhaustive study of nymphal and adult morphology, including both external and internal adult structures, and the first comparative study of male and female internal reproductive systems is included. Only two families are justified, the Tettigarctidae and Cicadidae. The latter are here considered to comprise three subfamilies, the Cicadinae, Cicadettinae n.stat. (= Tibicininae auct.) and the Tettigadinae (encompassing the Tibicinini, Platypediidae and Tettigadidae). Of particular note is the transfer of Tibicina Amyot, the type genus of the subfamily Tibicininae, to the subfamily Tettigadinae. The subfamily Plautillinae (containing only the genus Plautilla) is now placed at tribal rank within the Cicadinae. The subtribe Ydiellaria is raised to tribal rank. The American genus Magicicada Davis, previously of the tribe Tibicinini, now falls within the Taphurini. Three new tribes are recognized within the Australian fauna, the Tamasini n.tribe to accommodate Tamasa Distant and Parnkalla Distant, Jassopsaltriini n.tribe to accommodate Jassopsaltria Ashton and Burbungini n.tribe to accommodate Burbunga Distant. -
Molecular Phylogeny and Systematics of the Pieridae (Lepidoptera: Papilionoidea): Higher Classification and Biogeography
Blackwell Publishing LtdOxford, UKZOJZoological Journal of the Linnean Society0024-4082The Lin- nean Society of London, 2006? 2006 147? 239275 Original Article PHYLOGENY AND SYSTEMATICS OF THE PIERIDAEM. F. BRABY ET AL. Zoological Journal of the Linnean Society, 2006, 147, 239–275. With 8 figures Molecular phylogeny and systematics of the Pieridae (Lepidoptera: Papilionoidea): higher classification and Downloaded from https://academic.oup.com/zoolinnean/article-abstract/147/2/239/2631026 by Harvard Library user on 21 November 2018 biogeography MICHAEL F. BRABY1,2*, ROGER VILA1 and NAOMI E. PIERCE1 1Museum of Comparative Zoology, Harvard University, 26 Oxford St, Cambridge, MA 02138, USA 2School of Botany and Zoology, The Australian National University, Canberra, ACT 0200, Australia Received May 2004; accepted for publication October 2005 The systematic relationships of the butterfly family Pieridae are poorly understood. Much of our current under- standing is based primarily on detailed morphological observations made 50–70 years ago. However, the family and its putative four subfamilies and two tribes, have rarely been subjected to rigorous phylogenetic analysis. Here we present results based on an analysis of molecular characters used to reconstruct the phylogeny of the Pieridae in order to infer higher-level classification above the generic level and patterns of historical biogeography. Our sample contained 90 taxa representing 74 genera and six subgenera, or 89% of all genera recognized in the family. Three complementary approaches were -
Butterflies and Moths of Dominican Republic
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Ring Roads and Urban Biodiversity: Distribution of Butterflies in Urban
www.nature.com/scientificreports OPEN Ring roads and urban biodiversity: distribution of butterfies in urban parks in Beijing city and Received: 1 June 2018 Accepted: 26 April 2019 correlations with other indicator Published: xx xx xxxx species Kong-Wah Sing1,2, Jiashan Luo3, Wenzhi Wang1,2,4,5, Narong Jaturas6, Masashi Soga7, Xianzhe Yang8, Hui Dong9 & John-James Wilson10,6,8 The capital of China, Beijing, has a history of more than 800 years of urbanization, representing a unique site for studies of urban ecology. Urbanization can severely impact butterfy communities, yet there have been no reports of the species richness and distribution of butterfies in urban parks in Beijing. Here, we conducted the frst butterfy survey in ten urban parks in Beijing and estimated butterfy species richness. Subsequently, we examined the distribution pattern of butterfy species and analyzed correlations between butterfy species richness with park variables (age, area and distance to city center), and richness of other bioindicator groups (birds and plants). We collected 587 individual butterfies belonging to 31 species from fve families; 74% of the species were considered cosmopolitan. The highest butterfy species richness and abundance was recorded at parks located at the edge of city and species richness was signifcantly positively correlated with distance from city center (p < 0.05). No signifcant correlations were detected between the species richness and park age, park area and other bioindicator groups (p > 0.05). Our study provides the frst data of butterfy species in urban Beijing, and serves as a baseline for further surveys and conservation eforts. China is a megadiverse country but is rapidly losing biodiversity as a consequence of socioeconomic development and expansion of urban land since the 1990s1,2. -
Host Plant Choice Determined by Reproductive Interference Between Closely Related Butterflies
vol. 196, no. 4 the american naturalist october 2020 Host Plant Choice Determined by Reproductive Interference between Closely Related Butterflies Naota Ohsaki,1 Masaaki Ohata,2,* Yoshibumi Sato,3 andMarkD.Rausher4 1. Faculty of Agriculture, Kyoto University, Kyoto 606-8502, Japan; 2. Faculty of Bio-Environment, Kyoto University of Advanced Science, Kameoka, Kyoto 621-8555, Japan; 3. Kyoto College of Medical Science, Sonobe, Nantan, Kyoto 622-0041, Japan; 4. Department of Biology, Duke University, Durham, North Carolina 27705 Submitted September 20, 2019; Accepted April 29, 2020; Electronically published August 25, 2020 Dryad data: https://doi.org/10.5061/dryad.s7h44j149. abstract: A number of empirical studies have concluded that re- goku 2015; Noriyuki 2015). Although RI has sometimes productive interference (RI) contributes to parapatric species distri- been assumed to be infrequent (e.g., Mallet 2005), its oc- butions or sexual exclusion. However, the possibility that divergent currence has been demonstrated in many organisms, in- host plant use in phytophagous insects is due to sexual exclusion has cluding both animals and plants (Gröning and Hochkirch seldom been considered. Here, we present evidence that RI is re- 2008; Takakura et al. 2009; Takakura and Fujii 2015). sponsible for different host plant use by two Pierid butterfly species, Because RI reduces reproductive success and thus fit- Pieris napi and Pieris melete. When a novel host species was intro- ness, it is expected to often have both ecological and evo- duced about 50 years ago, two Pierid butterfly species at first used both the ancestral host species and the novel one. Subsequently, lutionary consequences. -
Science Journals — AAAS
SCIENCE ADVANCES | RESEARCH ARTICLE EVOLUTIONARY BIOLOGY Copyright © 2019 The Authors, some rights reserved; Unprecedented reorganization of holocentric exclusive licensee American Association chromosomes provides insights into the enigma of for the Advancement of Science. No claim to lepidopteran chromosome evolution original U.S. Government Jason Hill1,2*, Pasi Rastas3, Emily A. Hornett4,5,6, Ramprasad Neethiraj1, Nathan Clark7, Works. Distributed 8 1 9,10 under a Creative Nathan Morehouse , Maria de la Paz Celorio-Mancera , Jofre Carnicer Cols , Commons Attribution 11 7,12 1 1 13,14 Heinrich Dircksen , Camille Meslin , Naomi Keehnen , Peter Pruisscher , Kristin Sikkink , NonCommercial 9,10 15 1 1,16 17 Maria Vives , Heiko Vogel , Christer Wiklund , Alyssa Woronik , Carol L. Boggs , License 4.0 (CC BY-NC). Sören Nylin1, Christopher W. Wheat1* Chromosome evolution presents an enigma in the mega-diverse Lepidoptera. Most species exhibit constrained chromosome evolution with nearly identical haploid chromosome counts and chromosome-level gene collinearity among species more than 140 million years divergent. However, a few species possess radically inflated chromo- somal counts due to extensive fission and fusion events. To address this enigma of constraint in the face of an Downloaded from exceptional ability to change, we investigated an unprecedented reorganization of the standard lepidopteran chromosome structure in the green-veined white butterfly (Pieris napi). We find that gene content in P. napi has been extensively rearranged in large collinear blocks, which until now have been masked by a haploid chromosome number close to the lepidopteran average. We observe that ancient chromosome ends have been maintained and collinear blocks are enriched for functionally related genes suggesting both a mechanism and a possible role for selection in determining the boundaries of these genome-wide rearrangements. -
Revised Systematics and Higher Classification of Pierid Butterflies
Zoologica Scripta Revised systematics and higher classification of pierid butterflies (Lepidoptera: Pieridae) based on molecular data NIKLAS WAHLBERG,JADRANKA ROTA,MICHAEL F. BRABY,NAOMI E. PIERCE & CHRISTOPHER W. WHEAT Submitted: 5 May 2014 Wahlberg, N., Rota, J., Braby, M.F., Pierce, N.E. & Wheat, C.W. (2014). Revised Accepted: 12 July 2014 systematics and higher classification of pierid butterflies (Lepidoptera: Pieridae) based on doi:10.1111/zsc.12075 molecular data. — Zoologica Scripta, 43, 641–650. The butterfly family Pieridae comprises approximately 1000 described species placed in 85 genera, but the higher classification has not yet been settled. We used molecular data from eight gene regions (one mitochondrial and seven nuclear protein-coding genes) com- prising a total of ~6700 bp from 96 taxa to infer a well-supported phylogenetic hypothesis for the family. Based on this hypothesis, we revise the higher classification for all pierid genera. We resurrect the tribe Teracolini stat. rev. in the subfamily Pierinae to include the genera Teracolus, Pinacopteryx, Gideona, Ixias, Eronia, Colotis and most likely Calopieris. We transfer Hebomoia to the tribe Anthocharidini and assign the previously unplaced gen- era Belenois and Dixeia to the subtribe Aporiina. Three lineages near the base of Pierinae (Leptosia, Elodina and Nepheronia + Pareronia) remain unplaced. For each of these, we describe and delineate new tribes: Elodinini Braby tribus nova, Leptosiaini Braby tribus nova and Nepheroniini Braby tribus nova. The proposed higher classification is based on well-supported monophyletic groups and is likely to remain stable even with the addition of more data. Corresponding author: Niklas Wahlberg, Department of Biology, University of Turku, Turku, 20014, Finland. -
Artogeia) (Pieridae)
JOURNAL OF THE LEPIDOPTERISTS' SOCIETY Volume 33 1979 Number 2 Journal of the Lepidopterists' Society 33(2), 1979, 77-111 SUB SPECIFIC VARIATION IN BUTTERFLIES: ADAPTATION AND DISSECTED POLYMORPHISM IN PIERIS (ARTOGEIA) (PIERIDAE) S. R. BOWDEN 53, Crouch Hall Lane, Redbourn, Herts. AL3 7EU, England ABSTRACT. Subspecific variation of butterflies has in the past been attributed (with doubtful justification) to local ecological factors. In part I of this paper, main types of variation in wing-color and marking in the Artogeia napi-bryoniae melete group are described. Genetic control is relatively simple and known phenocopies result from environmental abnormalities unrelated to any actual local conditions. In part II, selective agents are considered to exercise little or no control over sub specific pattern-differences. Physiological adaptation is certain, but visible characters appear not to be specially adapted to present local conditions. In part III, the extreme selectionist position is rejected. Phenotypic differences have arisen historically, often in consequence of the dissection of polymorphisms, and are maintained by the succession of genetic path-choices in effectively isolated populations. Territorial changes have involved the retention of pattern-elements in biotopes far removed, geographically and ecolOgically, from the places of origin. Common possession of even superficial characters, when genetically identical, implies phylogenetic relationship. Some consequences of range-changes of populations are discussed. In this paper it will be maintained that wing-pattern (and other phenotypic) variation among subspecies of butterflies is generally con trolled not by present ecology but by factors having an historical aspect. Arguments will be related particularly to the group Artogeia napi + bryoniae + melete.