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Mass Emergence of the Tropical Swallowtail Moth Lyssa Zampa (Lepidoptera: Uraniidae: Uraniinae) in Singapore, with Notes on Its Partial Life History
20 TROP. LEPID. RES., 30(1): 20-27, 2020 JAIN & TEA: Mass emergence of Lyssa zampa Mass emergence of the tropical swallowtail moth Lyssa zampa (Lepidoptera: Uraniidae: Uraniinae) in Singapore, with notes on its partial life history Anuj Jain1,2, †,‡ and Yi-Kai Tea1,3,4 1Nature Society (Singapore), 510 Geylang Road, Singapore. 2Department of Biological Sciences, National University of Singapore, Singapore. 3School of Life and Environmental Sciences, University of Sydney, Sydney, Australia. 4Australian Museum Research Institute, 1 William Street, Sydney, New South Wales 2010, Australia. †Corresponding author: [email protected]; ‡Current affiliation: BirdLife International (Asia), #01-16/17, 354Tanglin Road, Singapore Date of issue online: 5 May 2020 Electronic copies (ISSN 2575-9256) in PDF format at: http://journals.fcla.edu/troplep; https://zenodo.org; archived by the Institutional Repository at the University of Florida (IR@UF), http://ufdc.ufl.edu/ufir;DOI : 10.5281/zenodo.3764165. © The author(s). This is an open access article distributed under the Creative Commons license CC BY-NC 4.0 (https://creativecommons.org/ licenses/by-nc/4.0/). Abstract: The tropical swallowtail uraniid moth Lyssa zampa is known to exhibit seasonal patterns of mass emergence throughout its range. These cyclical patterns of emergences are thought to correlate closely with oscillating host plant availability, as well as with interactions between herbivory and host plant defences. Because little has been reported concerning the biology of this species, the purpose of this paper is intended to serve as a starting point addressing the natural history of L. zampa in Singapore. Here we report on an instance of mass emergence of L. -
1 1 DNA Barcodes Reveal Deeply Neglected Diversity and Numerous
Page 1 of 57 1 DNA barcodes reveal deeply neglected diversity and numerous invasions of micromoths in 2 Madagascar 3 4 5 Carlos Lopez-Vaamonde1,2, Lucas Sire2, Bruno Rasmussen2, Rodolphe Rougerie3, 6 Christian Wieser4, Allaoui Ahamadi Allaoui 5, Joël Minet3, Jeremy R. deWaard6, Thibaud 7 Decaëns7, David C. Lees8 8 9 1 INRA, UR633, Zoologie Forestière, F- 45075 Orléans, France. 10 2 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261 CNRS Université de Tours, UFR 11 Sciences et Techniques, Tours, France. 12 3Institut de Systématique Evolution Biodiversité (ISYEB), Muséum national d'Histoire naturelle, 13 CNRS, Sorbonne Université, EPHE, 57 rue Cuvier, CP 50, 75005 Paris, France. 14 4 Landesmuseum für Kärnten, Abteilung Zoologie, Museumgasse 2, 9020 Klagenfurt, Austria 15 5 Department of Entomology, University of Antananarivo, Antananarivo 101, Madagascar 16 6 Centre for Biodiversity Genomics, University of Guelph, 50 Stone Road E., Guelph, ON 17 N1G2W1, Canada 18 7Centre d'Ecologie Fonctionnelle et Evolutive (CEFE UMR 5175, CNRS–Université de Genome Downloaded from www.nrcresearchpress.com by UNIV GUELPH on 10/03/18 19 Montpellier–Université Paul-Valéry Montpellier–EPHE), 1919 Route de Mende, F-34293 20 Montpellier, France. 21 8Department of Life Sciences, Natural History Museum, Cromwell Road, SW7 5BD, UK. 22 23 24 Email for correspondence: [email protected] For personal use only. This Just-IN manuscript is the accepted prior to copy editing and page composition. It may differ from final official version of record. 1 Page 2 of 57 25 26 Abstract 27 Madagascar is a prime evolutionary hotspot globally, but its unique biodiversity is under threat, 28 essentially from anthropogenic disturbance. -
DNA Barcodes Reveal Deeply Neglected Diversity and Numerous Invasions of Micromoths in Madagascar
Genome DNA barcodes reveal deeply neglected diversity and numerous invasions of micromoths in Madagascar Journal: Genome Manuscript ID gen-2018-0065.R2 Manuscript Type: Article Date Submitted by the 17-Jul-2018 Author: Complete List of Authors: Lopez-Vaamonde, Carlos; Institut National de la Recherche Agronomique (INRA), ; Institut de Recherche sur la Biologie de l’Insecte (IRBI), Sire, Lucas; Institut de Recherche sur la Biologie de l’Insecte Rasmussen,Draft Bruno; Institut de Recherche sur la Biologie de l’Insecte Rougerie, Rodolphe; Institut Systématique, Evolution, Biodiversité (ISYEB), Wieser, Christian; Landesmuseum für Kärnten Ahamadi, Allaoui; University of Antananarivo, Department Entomology Minet, Joël; Institut de Systematique Evolution Biodiversite deWaard, Jeremy; Biodiversity Institute of Ontario, University of Guelph, Decaëns, Thibaud; Centre d'Ecologie Fonctionnelle et Evolutive (CEFE UMR 5175, CNRS–Université de Montpellier–Université Paul-Valéry Montpellier–EPHE), , CEFE UMR 5175 CNRS Lees, David; Natural History Museum London Keyword: Africa, invasive alien species, Lepidoptera, Malaise trap, plant pests Is the invited manuscript for consideration in a Special 7th International Barcode of Life Issue? : https://mc06.manuscriptcentral.com/genome-pubs Page 1 of 57 Genome 1 DNA barcodes reveal deeply neglected diversity and numerous invasions of micromoths in 2 Madagascar 3 4 5 Carlos Lopez-Vaamonde1,2, Lucas Sire2, Bruno Rasmussen2, Rodolphe Rougerie3, 6 Christian Wieser4, Allaoui Ahamadi Allaoui 5, Joël Minet3, Jeremy R. deWaard6, Thibaud 7 Decaëns7, David C. Lees8 8 9 1 INRA, UR633, Zoologie Forestière, F- 45075 Orléans, France. 10 2 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261 CNRS Université de Tours, UFR 11 Sciences et Techniques, Tours, France. -
Fung Yuen SSSI & Butterfly Reserve Moth Survey 2009
Fung Yuen SSSI & Butterfly Reserve Moth Survey 2009 Fauna Conservation Department Kadoorie Farm & Botanic Garden 29 June 2010 Kadoorie Farm and Botanic Garden Publication Series: No 6 Fung Yuen SSSI & Butterfly Reserve moth survey 2009 Fung Yuen SSSI & Butterfly Reserve Moth Survey 2009 Executive Summary The objective of this survey was to generate a moth species list for the Butterfly Reserve and Site of Special Scientific Interest [SSSI] at Fung Yuen, Tai Po, Hong Kong. The survey came about following a request from Tai Po Environmental Association. Recording, using ultraviolet light sources and live traps in four sub-sites, took place on the evenings of 24 April and 16 October 2009. In total, 825 moths representing 352 species were recorded. Of the species recorded, 3 meet IUCN Red List criteria for threatened species in one of the three main categories “Critically Endangered” (one species), “Endangered” (one species) and “Vulnerable” (one species” and a further 13 species meet “Near Threatened” criteria. Twelve of the species recorded are currently only known from Hong Kong, all are within one of the four IUCN threatened or near threatened categories listed. Seven species are recorded from Hong Kong for the first time. The moth assemblages recorded are typical of human disturbed forest, feng shui woods and orchards, with a relatively low Geometridae component, and includes a small number of species normally associated with agriculture and open habitats that were found in the SSSI site. Comparisons showed that each sub-site had a substantially different assemblage of species, thus the site as a whole should retain the mosaic of micro-habitats in order to maintain the high moth species richness observed. -
Moths Light a Way? by John Pickering, Tori Staples and Rebecca Walcott
SOUTHERN LEPIDOPTERISTS NEWS VOLUME 38 NO4. (2016), PG. 331 SAVE ALL SPECIES – MOTHS LIGHT A WAY? BY JOHN PICKERING, TORI STAPLES AND REBECCA WALCOTT Abstract -- What would it take to save all species from snakes, and stinging insects, they pose no health risk. extinction? A new initiative, Save all species, plans to Moths are an exceedingly species-rich group, for which answer this question and provide the tools we need to do the diversity at a terrestrial site will typically exceed any so by 2050. Here we consider the merits and problems other taxon except for beetles. Because moth larvae are associated with inventorying moths to help decide which restricted in their diet to specific host taxa, differences in terrestrial areas to protect. We compare the the assemblages of resident moth species could reflect scientifically-described moth fauna of the British Isles differences across sites in plants and other hosts. If which, with 2,441 species, is taxonomically complete, that’s true, we may be able to use moth inventories as with 11,806 described species from North America north efficient proxies to compare surrounding plant of Mexico, the fauna of which is not fully described. As communities. a percentage of the described moth fauna, there are fewer “macro” moths (Geometroidea, Drepanoidea, Inventorying moths presents challenges, notably, Noctuoidea, Bombycoidea, Lasiocampidae) in the sampling smaller species, describing thousands of British Isles (34.9%) than those known for the United species new to science, and identifying specimens States and Canada (46.1%). We present data on 1,254 accurately. Our experience is that we can identify 99% species for an intensively-studied site in Clarke County, of moths from digital images to species, species-groups, Georgia and consider whether species in the British Isles which contain species of similar appearance, or are generally smaller than ones in Georgia. -
Fatty Acid-Amino Acid Conjugates Diversification in Lepidopteran Caterpillars
J Chem Ecol (2010) 36:319–325 DOI 10.1007/s10886-010-9764-8 Fatty Acid-amino Acid Conjugates Diversification in Lepidopteran Caterpillars Naoko Yoshinaga & Hans T. Alborn & Tomoaki Nakanishi & David M. Suckling & Ritsuo Nishida & James H. Tumlinson & Naoki Mori Received: 30 September 2009 /Revised: 29 January 2010 /Accepted: 11 February 2010 /Published online: 27 February 2010 # Springer Science+Business Media, LLC 2010 Abstract Fatty acid amino acid conjugates (FACs) have the presence of FACs in lepidopteran species outside these been found in noctuid as well as sphingid caterpillar oral families of agricultural interest is not well known. We con- secretions; in particular, volicitin [N-(17-hydroxylinolenoyl)- ducted FAC screening of 29 lepidopteran species, and found L-glutamine] and its biochemical precursor, N-linolenoyl-L- them in 19 of these species. Thus, FACs are commonly glutamine, are known elicitors of induced volatile emissions synthesized through a broad range of lepidopteran cater- in corn plants. These induced volatiles, in turn, attract natural pillars. Since all FAC-containing species had N-linolenoyl-L- enemies of the caterpillars. In a previous study, we showed glutamine and/or N-linoleoyl-L-glutamine in common, and that N-linolenoyl-L-glutamine in larval Spodoptera litura the evolutionarily earliest species among them had only plays an important role in nitrogen assimilation which might these two FACs, these glutamine conjugates might be the be an explanation for caterpillars synthesizing FACs despite evolutionarily older FACs. Furthermore, some species had an increased risk of attracting natural enemies. However, glutamic acid conjugates, and some had hydroxylated FACs. Comparing the diversity of FACs with lepidopteran phylog- eny indicates that glutamic acid conjugates can be synthe- N. -
SYSTEMATICS of the MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of T
SYSTEMATICS OF THE MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of the Requirements for The Degree of Doctor of Philosophy in the Graduate School of The Ohio State University By Sibyl Rae Bucheli, M.S. ***** The Ohio State University 2005 Dissertation Committee: Approved by Dr. John W. Wenzel, Advisor Dr. Daniel Herms Dr. Hans Klompen _________________________________ Dr. Steven C. Passoa Advisor Graduate Program in Entomology ABSTRACT The phylogenetics, systematics, taxonomy, and biology of Gelechioidea (Insecta: Lepidoptera) are investigated. This superfamily is probably the second largest in all of Lepidoptera, and it remains one of the least well known. Taxonomy of Gelechioidea has been unstable historically, and definitions vary at the family and subfamily levels. In Chapters Two and Three, I review the taxonomy of Gelechioidea and characters that have been important, with attention to what characters or terms were used by different authors. I revise the coding of characters that are already in the literature, and provide new data as well. Chapter Four provides the first phylogenetic analysis of Gelechioidea to include molecular data. I combine novel DNA sequence data from Cytochrome oxidase I and II with morphological matrices for exemplar species. The results challenge current concepts of Gelechioidea, suggesting that traditional morphological characters that have united taxa may not be homologous structures and are in need of further investigation. Resolution of this problem will require more detailed analysis and more thorough characterization of certain lineages. To begin this task, I conduct in Chapter Five an in- depth study of morphological evolution, host-plant selection, and geographical distribution of a medium-sized genus Depressaria Haworth (Depressariinae), larvae of ii which generally feed on plants in the families Asteraceae and Apiaceae. -
Butterflies of Ontario & Summaries of Lepidoptera
ISBN #: 0-921631-12-X BUTTERFLIES OF ONTARIO & SUMMARIES OF LEPIDOPTERA ENCOUNTERED IN ONTARIO IN 1991 BY A.J. HANKS &Q.F. HESS PRODUCTION BY ALAN J. HANKS APRIL 1992 CONTENTS 1. INTRODUCTION PAGE 1 2. WEATHER DURING THE 1991 SEASON 6 3. CORRECTIONS TO PREVIOUS T.E.A. SUMMARIES 7 4. SPECIAL NOTES ON ONTARIO LEPIDOPTERA 8 4.1 The Inornate Ringlet in Middlesex & Lambton Cos. 8 4.2 The Monarch in Ontario 8 4.3 The Status of the Karner Blue & Frosted Elfin in Ontario in 1991 11 4.4 The West Virginia White in Ontario in 1991 11 4.5 Butterfly & Moth Records for Kettle Point 11 4.6 Butterflies in the Hamilton Study Area 12 4.7 Notes & Observations on the Early Hairstreak 15 4.8 A Big Day for Migrants 16 4.9 The Ocola Skipper - New to Ontario & Canada .17 4.10 The Brazilian Skipper - New to Ontario & Canada 19 4.11 Further Notes on the Zarucco Dusky Wing in Ontario 21 4.12 A Range Extension for the Large Marblewing 22 4.13 The Grayling North of Lake Superior 22 4.14 Description of an Aberrant Crescent 23 4.15 A New Foodplant for the Old World Swallowtail 24 4.16 An Owl Moth at Point Pelee 25 4.17 Butterfly Sampling in Algoma District 26 4.18 Record Early Butterfly Dates in 1991 26 4.19 Rearing Notes from Northumberland County 28 5. GENERAL SUMMARY 29 6. 1990 SUMMARY OF ONTARIO BUTTERFLIES, SKIPPERS & MOTHS 32 Hesperiidae 32 Papilionidae 42 Pieridae 44 Lycaenidae 48 Libytheidae 56 Nymphalidae 56 Apaturidae 66 Satyr1dae 66 Danaidae 70 MOTHS 72 CONTINUOUS MOTH CYCLICAL SUMMARY 85 7. -
The Evolution, Diversity, and Host Associations of Rhabdoviruses Ben Longdon,1,* Gemma G
Virus Evolution, 2015, 1(1): vev014 doi: 10.1093/ve/vev014 Research article The evolution, diversity, and host associations of rhabdoviruses Ben Longdon,1,* Gemma G. R. Murray,1 William J. Palmer,1 Jonathan P. Day,1 Darren J Parker,2,3 John J. Welch,1 Darren J. Obbard4 and Francis M. Jiggins1 1 2 Department of Genetics, University of Cambridge, Cambridge, CB2 3EH, School of Biology, University of Downloaded from St Andrews, St Andrews, KY19 9ST, UK, 3Department of Biological and Environmental Science, University of Jyva¨skyla¨, Jyva¨skyla¨, Finland and 4Institute of Evolutionary Biology, and Centre for Immunity Infection and Evolution, University of Edinburgh, Edinburgh, EH9 3JT, UK *Corresponding author: E-mail: [email protected] http://ve.oxfordjournals.org/ Abstract Metagenomic studies are leading to the discovery of a hidden diversity of RNA viruses. These new viruses are poorly characterized and new approaches are needed predict the host species these viruses pose a risk to. The rhabdoviruses are a diverse family of RNA viruses that includes important pathogens of humans, animals, and plants. We have discovered thirty-two new rhabdoviruses through a combination of our own RNA sequencing of insects and searching public sequence databases. Combining these with previously known sequences we reconstructed the phylogeny of 195 rhabdovirus by guest on December 14, 2015 sequences, and produced the most in depth analysis of the family to date. In most cases we know nothing about the biology of the viruses beyond the host they were identified from, but our dataset provides a powerful phylogenetic approach to predict which are vector-borne viruses and which are specific to vertebrates or arthropods. -
Modular Structure, Sequence Diversification and Appropriate
www.nature.com/scientificreports OPEN Modular structure, sequence diversifcation and appropriate nomenclature of seroins produced Received: 17 July 2018 Accepted: 14 February 2019 in the silk glands of Lepidoptera Published: xx xx xxxx Lucie Kucerova1, Michal Zurovec 1,2, Barbara Kludkiewicz1, Miluse Hradilova3, Hynek Strnad3 & Frantisek Sehnal1,2 Seroins are small lepidopteran silk proteins known to possess antimicrobial activities. Several seroin paralogs and isoforms were identifed in studied lepidopteran species and their classifcation required detailed phylogenetic analysis based on complete and verifed cDNA sequences. We sequenced silk gland-specifc cDNA libraries from ten species and identifed 52 novel seroin cDNAs. The results of this targeted research, combined with data retrieved from available databases, form a dataset representing the major clades of Lepidoptera. The analysis of deduced seroin proteins distinguished three seroin classes (sn1-sn3), which are composed of modules: A (includes the signal peptide), B (rich in charged amino acids) and C (highly variable linker containing proline). The similarities within and between the classes were 31–50% and 22.5–25%, respectively. All species express one, and in exceptional cases two, genes per class, and alternative splicing further enhances seroin diversity. Seroins occur in long versions with the full set of modules (AB1C1B2C2B3) and/or in short versions that lack parts or the entire B and C modules. The classes and the modular structure of seroins probably evolved prior to the split between Trichoptera and Lepidoptera. The diversity of seroins is refected in proposed nomenclature. Te silk spun by caterpillars is a composite material based on two protein agglomerates that have been known for centuries as fbroin and sericin. -
Lepidoptera of North America 5
Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains, -
Big Creek Lepidoptera Checklist
Big Creek Lepidoptera Checklist Prepared by J.A. Powell, Essig Museum of Entomology, UC Berkeley. For a description of the Big Creek Lepidoptera Survey, see Powell, J.A. Big Creek Reserve Lepidoptera Survey: Recovery of Populations after the 1985 Rat Creek Fire. In Views of a Coastal Wilderness: 20 Years of Research at Big Creek Reserve. (copies available at the reserve). family genus species subspecies author Acrolepiidae Acrolepiopsis californica Gaedicke Adelidae Adela flammeusella Chambers Adelidae Adela punctiferella Walsingham Adelidae Adela septentrionella Walsingham Adelidae Adela trigrapha Zeller Alucitidae Alucita hexadactyla Linnaeus Arctiidae Apantesis ornata (Packard) Arctiidae Apantesis proxima (Guerin-Meneville) Arctiidae Arachnis picta Packard Arctiidae Cisthene deserta (Felder) Arctiidae Cisthene faustinula (Boisduval) Arctiidae Cisthene liberomacula (Dyar) Arctiidae Gnophaela latipennis (Boisduval) Arctiidae Hemihyalea edwardsii (Packard) Arctiidae Lophocampa maculata Harris Arctiidae Lycomorpha grotei (Packard) Arctiidae Spilosoma vagans (Boisduval) Arctiidae Spilosoma vestalis Packard Argyresthiidae Argyresthia cupressella Walsingham Argyresthiidae Argyresthia franciscella Busck Argyresthiidae Argyresthia sp. (gray) Blastobasidae ?genus Blastobasidae Blastobasis ?glandulella (Riley) Blastobasidae Holcocera (sp.1) Blastobasidae Holcocera (sp.2) Blastobasidae Holcocera (sp.3) Blastobasidae Holcocera (sp.4) Blastobasidae Holcocera (sp.5) Blastobasidae Holcocera (sp.6) Blastobasidae Holcocera gigantella (Chambers) Blastobasidae