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Lepidoptera, Endromidae) in China
A peer-reviewed open-access journal ZooKeys 127: 29–42 (2011)The genusAndraca (Lepidoptera, Endromidae) in China... 29 doi: 10.3897/zookeys.127.928 RESEARCH artICLE www.zookeys.org Launched to accelerate biodiversity research The genus Andraca (Lepidoptera, Endromidae) in China with descriptions of a new species Xing Wang1,†, Ling Zeng2,‡, Min Wang2,§ 1 Department of Entomology, South China Agricultural University, Guangzhou, Guangdong 510640, P.R. China. Present address: Institute of Entomology, College of Biosafety Science and Technology, Hunan Agricul- tural University, Changsha 410128 Hunan, China; and Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Changsha 410128, Hunan, China 2 Department of Entomology, South China Agricultural University, Guangzhou, Guangdong 510640, P.R. China † urn:lsid:zoobank.org:author:F8727887-0014-42D4-BA68-21B3009E8C7F ‡ urn:lsid:zoobank.org:author:7981BF0E-D1F8-43CA-A505-72DBBA140023 § urn:lsid:zoobank.org:author:D683614E-1F58-4CA8-9D80-B23BD41947A2 Corresponding author: Ling Zeng ([email protected]) Academic editor: N. Wahlberg | Received 21 January 2011 | Accepted 15 August 2011 | Published 8 September 2011 urn:lsid:zoobank.org:pub:33D4BBFB-4B7D-4BBC-B34C-17D2E7F99F67 Citation: Wang X, Zeng L, Wang M (2011) The genus Andraca (Lepidoptera, Endromidae) in China with descriptions of a new species. ZooKeys 127: 29–42. doi: 10.3897/zookeys.127.928 Abstract The six species of the genus Andraca Walker hitherto known from China are reviewed, and a new species, A. gongshanensis, sp. n., described from Yunnan Province, China. Adults and male genitalia of all exam- ined species are illustrated, together with a distributional map. A key to all seven Chinese Andraca species is provided. -
The Mcguire Center for Lepidoptera and Biodiversity
Supplemental Information All specimens used within this study are housed in: the McGuire Center for Lepidoptera and Biodiversity (MGCL) at the Florida Museum of Natural History, Gainesville, USA (FLMNH); the University of Maryland, College Park, USA (UMD); the Muséum national d’Histoire naturelle in Paris, France (MNHN); and the Australian National Insect Collection in Canberra, Australia (ANIC). Methods DNA extraction protocol of dried museum specimens (detailed instructions) Prior to tissue sampling, dried (pinned or papered) specimens were assigned MGCL barcodes, photographed, and their labels digitized. Abdomens were then removed using sterile forceps, cleaned with 100% ethanol between each sample, and the remaining specimens were returned to their respective trays within the MGCL collections. Abdomens were placed in 1.5 mL microcentrifuge tubes with the apex of the abdomen in the conical end of the tube. For larger abdomens, 5 mL microcentrifuge tubes or larger were utilized. A solution of proteinase K (Qiagen Cat #19133) and genomic lysis buffer (OmniPrep Genomic DNA Extraction Kit) in a 1:50 ratio was added to each abdomen containing tube, sufficient to cover the abdomen (typically either 300 µL or 500 µL) - similar to the concept used in Hundsdoerfer & Kitching (1). Ratios of 1:10 and 1:25 were utilized for low quality or rare specimens. Low quality specimens were defined as having little visible tissue inside of the abdomen, mold/fungi growth, or smell of bacterial decay. Samples were incubated overnight (12-18 hours) in a dry air oven at 56°C. Importantly, we also adjusted the ratio depending on the tissue type, i.e., increasing the ratio for particularly large or egg-containing abdomens. -
Phylogenomics Reveals Major Diversification Rate Shifts in The
bioRxiv preprint doi: https://doi.org/10.1101/517995; this version posted January 11, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Phylogenomics reveals major diversification rate shifts in the evolution of silk moths and 2 relatives 3 4 Hamilton CA1,2*, St Laurent RA1, Dexter, K1, Kitching IJ3, Breinholt JW1,4, Zwick A5, Timmermans 5 MJTN6, Barber JR7, Kawahara AY1* 6 7 Institutional Affiliations: 8 1Florida Museum of Natural History, University of Florida, Gainesville, FL 32611 USA 9 2Department of Entomology, Plant Pathology, & Nematology, University of Idaho, Moscow, ID 10 83844 USA 11 3Department of Life Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK 12 4RAPiD Genomics, 747 SW 2nd Avenue #314, Gainesville, FL 32601. USA 13 5Australian National Insect Collection, CSIRO, Clunies Ross St, Acton, ACT 2601, Canberra, 14 Australia 15 6Department of Natural Sciences, Middlesex University, The Burroughs, London NW4 4BT, UK 16 7Department of Biological Sciences, Boise State University, Boise, ID 83725, USA 17 *Correspondence: [email protected] (CAH) or [email protected] (AYK) 18 19 20 Abstract 21 The silkmoths and their relatives (Bombycoidea) are an ecologically and taxonomically 22 diverse superfamily that includes some of the most charismatic species of all the Lepidoptera. 23 Despite displaying some of the most spectacular forms and ecological traits among insects, 24 relatively little attention has been given to understanding their evolution and the drivers of 25 their diversity. -
Characteristics Involved in Conformers of Bombykol and Its Derivatives
Proc. Nat. Acad. Sci. USA Vol. 72, No. 9, pp. 3337-341, September 1975 Biochemistry Correlation of moth sex pheromone activities with molecular characteristics involved in conformers of bombykol and its derivatives (olfaction/conformational analysis) TOSHIHIDE KIKUCHI Department of Biological Science, Tohoku University, Kawauchi, Sendai 980, Japan Communicated by V. C. Dethier, June 6,1975 ABSTRACT Molecular characteristics of bombykol and distance between functional groups involved in these com- its 11 derivatives, which reveal significant correlations with pounds depends upon their conformations as well as their biological activities for single sex pheromone receptor cells configurations. With considerations of frequency distribu- of four moth species, Bombyx mori, Aglia tau, Endromis versicolora, and Deileplila euphorbiae, were examined on tion patterns of the distances between a pair of methyl and the assumption of the "bifunctional unit model." Probabili- hydroxyl groups involved with conformers of bombykol and ties of bifunctional unit formations of those 12 compounds its derivatives, the attempts described below could provide were assessed with frequency distribution patterns of dis- demonstrations on the relationships between pheromone ac- tances between the proton acceptor, the proton donor, and tivities and their molecular characteristics. the methyl group involved in a total of 1,200 conformers. A highly significant correlation exists between biological activ- ity for each species and the probability of a particular bi- functional -
Long-Term Changes to the Frequency of Occurrence of British Moths Are Consistent with Opposing and Synergistic Effects of Climate and Land-Use Changes
Journal of Applied Ecology 2014, 51, 949–957 doi: 10.1111/1365-2664.12256 Long-term changes to the frequency of occurrence of British moths are consistent with opposing and synergistic effects of climate and land-use changes Richard Fox1*, Tom H. Oliver2, Colin Harrower2, Mark S. Parsons1, Chris D. Thomas3 and David B. Roy2 1Butterfly Conservation, Manor Yard, Wareham, Dorset, BH20 5QP, UK; 2NERC Centre for Ecology & Hydrology, Maclean Building, Benson Lane, Crowmarsh Gifford, Wallingford, Oxfordshire, OX10 8BB, UK; and 3Department of Biology, University of York, York, YO10 5DD, UK Summary 1. Species’ distributions are likely to be affected by a combination of environmental drivers. We used a data set of 11 million species occurrence records over the period 1970–2010 to assess changes in the frequency of occurrence of 673 macro-moth species in Great Britain. Groups of species with different predicted sensitivities showed divergent trends, which we interpret in the context of land-use and climatic changes. 2. A diversity of responses was revealed: 260 moth species declined significantly, whereas 160 increased significantly. Overall, frequencies of occurrence declined, mirroring trends in less species-rich, yet more intensively studied taxa. 3. Geographically widespread species, which were predicted to be more sensitive to land use than to climate change, declined significantly in southern Britain, where the cover of urban and arable land has increased. 4. Moths associated with low nitrogen and open environments (based on their larval host plant characteristics) declined most strongly, which is also consistent with a land-use change explanation. 5. Some moths that reach their northern (leading edge) range limit in southern Britain increased, whereas species restricted to northern Britain (trailing edge) declined significantly, consistent with a climate change explanation. -
Insecta: Lepidoptera)
Biodiversity Data Journal 6: e22236 doi: 10.3897/BDJ.6.e22236 Taxonomic Paper A global checklist of the Bombycoidea (Insecta: Lepidoptera) Ian J Kitching‡, Rodolphe Rougerie§, Andreas Zwick |, Chris A Hamilton¶, Ryan A St Laurent¶, Stefan Naumann#, Liliana Ballesteros Mejia§,¤, Akito Y Kawahara¶ ‡ Natural History Museum, London, United Kingdom § Muséum national d’Histoire naturelle, Sorbonne Université, Institut de Systématique, Evolution, Biodiversité (ISYEB), UMR 7205 – CNRS, MNHN, UPMC, EPHE, Paris, France | CSIRO - Australian National Insect Collection, Canberra, Australia ¶ Florida Museum of Natural History, University of Florida, Gainesville, United States of America # Hochkirchstrasse 71, Berlin, Germany ¤ CESAB, Centre de Synthèse et d'Analyse sur la Biodiversité, Aix-en-Provence, France Corresponding author: Ian J Kitching ([email protected]), Rodolphe Rougerie ([email protected]) Academic editor: Yasen Mutafchiev Received: 13 Nov 2017 | Accepted: 08 Feb 2018 | Published: 12 Feb 2018 Citation: Kitching I, Rougerie R, Zwick A, Hamilton C, St Laurent R, Naumann S, Ballesteros Mejia L, Kawahara A (2018) A global checklist of the Bombycoidea (Insecta: Lepidoptera). Biodiversity Data Journal 6: e22236. https://doi.org/10.3897/BDJ.6.e22236 ZooBank: urn:lsid:zoobank.org:pub:937DDBF7-10F3-4700-B188-227F33800216 Abstract Background Bombycoidea is an ecologically diverse and speciose superfamily of Lepidoptera. The superfamily includes many model organisms, but the taxonomy and classification of the superfamily has remained largely in disarray. Here we present a global checklist of Bombycoidea. Following Zwick (2008) and Zwick et al. (2011), ten families are recognized: Anthelidae, Apatelodidae, Bombycidae, Brahmaeidae, Carthaeidae, Endromidae, Eupterotidae, Phiditiidae, Saturniidae and Sphingidae. The former families Lemoniidae and Mirinidae are included within Brahmaeidae and Endromidae respectively. -
Insecta: Lepidoptera
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Natural History Museum Repository Title A global checklist of the Bombycoidea (Insecta: Lepidoptera). Authors Kitching, IJ; Rougerie, R; Zwick, A; Hamilton, CA; St Laurent, RA; Naumann, S; Ballesteros Mejia, L; Kawahara, AY Description This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. The attached file is the published pdf plus supplementary data file. Date Submitted 2018-02-16 Biodiversity Data Journal 6: e22236 doi: 10.3897/BDJ.6.e22236 Taxonomic Paper A global checklist of the Bombycoidea (Insecta: Lepidoptera) Ian J Kitching‡, Rodolphe Rougerie§, Andreas Zwick |, Chris A Hamilton¶, Ryan A St Laurent¶, Stefan Naumann#, Liliana Ballesteros Mejia§,¤, Akito Y Kawahara¶ ‡ Natural History Museum, London, United Kingdom § Muséum national d’Histoire naturelle, Sorbonne Université, Institut de Systématique, Evolution, Biodiversité (ISYEB), UMR 7205 – CNRS, MNHN, UPMC, EPHE, Paris, France | CSIRO - Australian National Insect Collection, Canberra, Australia ¶ Florida Museum of Natural History, University of Florida, Gainesville, United States of America # Hochkirchstrasse 71, Berlin, Germany ¤ CESAB, Centre de Synthèse et d'Analyse sur la Biodiversité, Aix-en-Provence, France Corresponding author: Ian J Kitching ([email protected]), Rodolphe Rougerie ([email protected]) Academic editor: Yasen Mutafchiev Received: 13 Nov 2017 | Accepted: 08 Feb 2018 | Published: 12 Feb 2018 Citation: Kitching I, Rougerie R, Zwick A, Hamilton C, St Laurent R, Naumann S, Ballesteros Mejia L, Kawahara A (2018) A global checklist of the Bombycoidea (Insecta: Lepidoptera). -
Heteroceran Fauna of Mt. Okdolbong, Gyeongbuk, Korea (Lepidoptera)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Journal of Asia-Pacific Biodiversity Vol. 6, No. 2 329-337, 2013 http://dx.doi.org/10.7229/jkn.2013.6.2.329 Heteroceran Fauna of Mt. Okdolbong, Gyeongbuk, Korea (Lepidoptera) Seung-Jin Roh, Sat-Byul Shin, Young-Min Shin, Jun-Hwoung Jeon and Bong-Kyu Byun* Department of Biological Science and Biotechnology, Hannam University, 461-6 Jeonmin-dong, Yuseong-gu, Daejeon 305-811, Korea Abstract: This study aims to obtain the basic data for studies on changes in insect fauna and insect resources around Mt. Okdolbong in Bongwha, Gyeongbuk, where a national arboretum is planned to be constructed, through investigating the insect fauna and obtaining its evidence samples. In particular, this region is very important for studies on biodiversity and its preservation, and requires fundamental data for related studies such as investigations of vulnerable species and changes in their distribution associated with climatic changes. A total of 263 species including 1,689 individuals of moths was collected in this study. The most dominant species was Endotricha loivaceali with 222 individuals, and was followed by Hydrillodes morose with 97 individuals and Craneophora ficki with 86 individuals. Keywords: forest insects, insect fauna, dominant species, specimen Introduction on insect resources in the regions, except a recent study on nearby Mt. Okdolbong (Roh et al., 2012). We investigated The survey regions in this study is located in Bongwha, the insect fauna in the regions where a national arboretum Gyeongbuk. The northern boundary of Bongwha is the is to be constructed, and collected insects to obtain the basic starting point where Sobaek Mountains branches from data for studies on changes in insect fauna and insect Taebaek Mountains that include high mountains such as resources in the regions. -
Formosan Entomologist Journal Homepage: Entsocjournal.Yabee.Com.Tw
DOI:10.6662/TESFE.202002_40(1).002 台灣昆蟲 Formosan Entomol. 40: 10-83 (2020) 研究報告 Formosan Entomologist Journal Homepage: entsocjournal.yabee.com.tw An Annotated Checklist of Macro Moths in Mid- to High-Mountain Ranges of Taiwan (Lepidoptera: Macroheterocera) Shipher Wu1*, Chien-Ming Fu2, Han-Rong Tzuoo3, Li-Cheng Shih4, Wei-Chun Chang5, Hsu-Hong Lin4 1 Biodiversity Research Center, Academia Sinica, Taipei 2 No. 8, Tayuan 7th St., Taiping, Taichung 3 No. 9, Ln. 133, Chung Hsiao 3rd Rd., Puli, Nantou 4 Endemic Species Research Institute, Nantou 5 Taipei City Youth Development Office, Taipei * Corresponding email: [email protected] Received: 21 February 2020 Accepted: 14 May 2020 Available online: 26 June 2020 ABSTRACT The aim of the present study was to provide an annotated checklist of Macroheterocera (macro moths) in mid- to high-elevation regions (>2000 m above sea level) of Taiwan. Although such faunistic studies were conducted extensively in the region during the first decade of the early 20th century, there are a few new taxa, taxonomic revisions, misidentifications, and misspellings, which should be documented. We examined 1,276 species in 652 genera, 59 subfamilies, and 15 families. We propose 4 new combinations, namely Arichanna refracta Inoue, 1978 stat. nov.; Psyra matsumurai Bastelberger, 1909 stat. nov.; Olene baibarana (Matsumura, 1927) comb. nov.; and Cerynia usuguronis (Matsumura, 1927) comb. nov.. The noctuid Blepharita alpestris Chang, 1991 is regarded as a junior synonym of Mamestra brassicae (Linnaeus, 1758) (syn. nov.). The geometrids Palaseomystis falcataria (Moore, 1867 [1868]), Venusia megaspilata (Warren, 1895), and Gandaritis whitelyi (Butler, 1878) and the erebid Ericeia elongata Prout, 1929 are newly recorded in the fauna of Taiwan. -
Insecta, Lepidoptera, Bombycoidea) from Mainland China, Taiwan and Hainan Islands
Zootaxa 3989 (1): 001–138 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2015 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3989.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:9BCFFC47-43D1-47B8-BA56-70A129E6A63F ZOOTAXA 3989 The fauna of the family Bombycidae sensu lato (Insecta, Lepidoptera, Bombycoidea) from Mainland China, Taiwan and Hainan Islands XING WANG1, 2, 3, MIN WANG4, VADIM V. ZOLOTUHIN5, TOSHIYA HIROWATARI3, SHIPHER WU6 & GUO-HUA HUANG1, 2, 3 1Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Changsha, Hunan 410128, Mainland China. E-mail: [email protected] 2College of Plant Protection, Hunan Agricultural University, Changsha, Hunan 410128, Mainland China. E-mail: [email protected] 3Entomological Laboratory, Faculty of Agriculture, Kyushu University, 6-10-1 Hakozaki, Fukuoka 812-8581, Japan. E-mail: [email protected] 4Department of Entomology, South China Agricultural University, Guangzhou, Guangdong 510640, Mainland China. E-mail: [email protected] 5Department of Zoology, State Pedagogical University of Ulyanovsk, pl. Lenina 4, RUS-432700, Ulyanovsk, Russia. E-mail: [email protected] 6Biodiversity Research Center, Academia Sinica, Taiwan. Address: No.128, Sec. 2, Academia Rd., Nangang Dist., Taipei City 11529, Taiwan. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by M. Pellinen: 28 Apr. 2015; published: 22 Jul. 2015 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 XING WANG, MIN WANG, VADIM V. ZOLOTUHIN, TOSHIYA HIROWATARI, SHIPHER WU & GUO- HUA HUANG The fauna of the family Bombycidae sensu lato (Insecta, Lepidoptera, Bombycoidea) from Mainland China, Taiwan and Hainan Islands (Zootaxa 3989) 138 pp.; 30 cm. -
Taxonomy Principles and Methods
Taxonomy Principles and Methods Taxonomy ......................................................................................................................................................1 Classification .................................................................................................................................................2 Systematics ....................................................................................................................................................3 Zoological nomenclature ..........................................................................................................................3 Classification of insects .............................................................................................................................4 Insect morphology ......................................................................................................................................4 Insect life stages and development ................................................................................................... 16 How to identify an insect ....................................................................................................................... 18 Taxonomy Taxonomy is the science of classifying organisms. Taxonomy results in classifications, which allow for storage, retrieval and communication of information about organisms. A key function of taxonomy is to provide correct identification of organisms. This workshop introduces participants to the -
The Miridae (Hemiptera : Heteroptera) Associated with Noble
AN ABSTRACT OF THE THESIS OF Gary Michael Cooper for the degree of Master of Science in Entomology presented in January 1981 Title: The Miridae (Hemiptera:Heteroptera) Associated with Noble Fir, Abies procera Rehd. Redacted for Privacy Abstract approved: /- Dr. John D. Lattin The Miridae, or plant bugs, associated with noble fir, Abies procera Rehd., are discussed. Thirty six species of the Miridae were collected from noble fir. Twenty five of these species are considered only "visitors" to noble fir. The study does not deal with these species. Noble fir is a host of the eleven other species: Deraeocoris incertus Knight, Deraeocoris piceicola Knight, Dichrooscytus sp. A, Orthotylus sp. A, Paradacerla formicina (Parshley), Phytocoris neglectus Knight, Phytocoris sp. A, Pinalitus solivagus (Van Duzee), Plagiognathus sp. A and Psallus spp. A and B. Fifth instar larvae and the adults of these eleven species were examined and described. The plant bugs were collected from the noble fir foliage every seven to fourteen days from early May to mid-October,1979 from Marys Peak in the Oregon Coast Range and the H.J. Andrews Experimental Forest in the Oregon Cascade Mountains. Distributional data were added from collecting trips in Oregon on Grass Mountain and around Mt. Hood and in Washington state at White Pass and Stevens Pass. The larvae and adults of the eleven noble fir mirid species were observed in a growth chamber. Feeding observations were recorded for eight species. The larvae and adults were examined for external signs of insect parasitism. Sticky traps placed on the boles of noble fir trees on Marys Peak collected very few mirids, suggestingthat the mirids remain on the foliage and branches.