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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. -
Description of a New Species of Eupterote(Eupterote) from Sulawesi
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Nachrichten des Entomologischen Vereins Apollo Jahr/Year: 2010 Band/Volume: 31 Autor(en)/Author(s): Nässig Wolfgang A., Holloway Jeremy D., Beeke Martin Artikel/Article: Description of a new species of Eupterote (Eupterote) from Sulawesi (Indonesia) (Lepidoptera: Eupterotidae) 197-200 Nachr. entomol. Ver. Apollo, N. F. 31 (4): 197–200 (2011) 197 Description of a new species of Eupterote(Eupterote) from Sulawesi (Indonesia) (Lepidoptera: Eupterotidae) Wolfgang A. Nässig1, Jeremy D. Holloway and Martin Beeke Dr. Wolfgang A. Nässig, Entomologie II, Forschungsinstitut Senckenberg, Senckenberganlage 25, D60325 Frankfurt am Main, Germany; [email protected] Dr. Jeremy D. Holloway, Department of Entomology, Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom; [email protected] Martin Beeke, Buchhofstrasse 33, D32351 Stemwede, Germany Abstract: Further data on the Eupterotidae fauna of the barcodebas ed studies on the Eu pte ro t i dae of Asia; the In do ne si an is lands of Sulawesi and Bu ton is provided. A pre sent pa per is a preliminary pub li ca tion to de scribe a Eupterote new nocturnal species of the ge nus Hübner, 1820 clearly un named and easily re cog niz ed new spe cies from [“1816”], nominotypical sub ge nus, is described: Eupterote (Eu pterote) celebica sp. n. (ho lo ty pe male in SMFL, Frank Sulawesi in advance of the revisions. Re vi sio n al no tes on furt am Main) from Su la we si Selatan, Tanah Toraja, Pu lu the entire group, based on the results of our stu dies, will Pu lu, ca. -
Contribution of Museums, Census, Mapping, High Resolution Photographs and Audio-Recording to the Extinction of Endangered Species
International Journal of Scientific and Research Publications, Volume 8, Issue 1, January 2018 288 ISSN 2250-3153 Contribution of museums, census, mapping, high resolution photographs and audio-recording to the extinction of endangered species Kavita Taneja and *Geetanjali Dhawan Department of Zoology, D.B.G.Government College, Panipat-132103 *Department of Zoology, Arya P.G College, Panipat-132103 Abstract- To cope with extinction crisis, museums have a risk but in the present study the endangered species have been crucial role to play in preserving the life of every possible categorised as very likely to become extinct. individual. Museum collections provide essential verifiable evidence of species occurrence over time and space and thus Why so many techniques are studied? permit rigorous taxonomic, biological and ecological Because of simplicity of these techniques one or two are investigations. Two of the basic tasks required for census are not enough to combat this worldwide problem. In certain gathering data on presence and abundance. By placing stickers instances, an admixture of two or three are required to justify on the wing of insect with identification information, migration specific goal. patterns of insect including how far and where they fly is studied. Using mapping and visualization tools, endangered species and What is extinction? their vital habitats are protected. A new computer technology i.e. The moment of extinction is generally considered to be the remote monitoring of wildlife sounds is used to listen multiple death of the last individual of the species, although the capacity bird sounds. Thus, sound changes due to habitat loss or climate to breed and recover may have been lost before this point. -
Rachita Genitalial Morphology 1451
CASE REPORT ZOOS' PRINT JOURNAL 21(8): 2343-2346 GENITALIAL MORPHOLOGY OF SOME EUPTEROTIDAE (LEPIDOPTERA) FROM SHIVALIKS IN INDIA Rachita Sood ¹, H.S. Rose ² and P.C. Pathania ³ ¹,² Department of Zoology, Punjabi University, Patiala, Punjab 147002, India ³ Division of Entomology, Indian Agricultural Research Institute, New Delhi 110012, India Email: ³ [email protected] (corresponding author) ABSTRACT Description of external genitalia of species studied External genitalial morphology of five species of Eupterotidae namely, Apona cashmirensis Kollar, Eupterote undata Apona Walker Blanchard, Eupterote assimilis Moore, Eupterote fraterna Moore, and Eupterote decorata Moore were studied and a Apona Walker, 1856, List Specimens Lepid. Insects Colln. Br. key for their identification is presented in this paper. Mus., 7 : 1762. KEYWORDS Type species: Apona pallida Walker, 1856, ibidem, 7 : 1763, by Eupterotidae, genitalia, India, key, Lepidoptera. monotypy. Holloway (1987) mentions Eupteroidea as a small but most Apona cashmirensis Kollar diverse tropical group of moths in Africa and the Oriental region. Apona cashmirensis Kollar, 1848, In Hügel Kashmir, 4 : 472, Moths belonging to this superfamily are characterized by the pl. 21, fig. 4. forewings possessing a series of indistinct waved lines (fasciations), out of which the double postmedial may be Material examined consistent. The hindwings too have such patterns which may Two males, 25.vii.2000, Nangal, Roopnagar District, Punjab, be somewhat reduced and simple. All the fasciations may be 370m, coll. Rachita Sood & P.C. Pathania clear or none may be clear, even in the specimens collected from the same locality (Hampson, 1892). During the course of Distribution the present study, a phenon comprising of 14 individuals were North-West Himalayas and Sikkim (Hampson, 1892). -
Sapium Sebiferum Triadica Sebifera Chinese Tallow Tree
Sapium sebiferum Triadica sebifera Chinese tallow tree Introduction The genus Sapium consists of approximately 120 species worldwide. Members of the genus occur primarily in tropical regions, especially in South America. Nine species occur in the low hills of southeastern and southwestern China[16]. Taxonomy Order: Geraniales Suborder: Euphorbiineae Species of Sapium in China Family: Euphorbiaceae Scientific Name Scientific Name Subfamily: Euphorbioideae S. sebiferum (L.) Roxb. S. insigne (Royle) Benth. ex Hook. f. Tribe: Hippomaneae Reichb. Genus: Sapium P. Br. S. atrobadiomaculatum Metcalf S. japonicum (Sieb. et Zucc.) Pax et Section: Triadica (Lour.) Muell. S. baccatum Roxb. Hoffm.(Sieb.) Arg S. chihsinianum S. K. Lee S. pleiocarpum Y. C. Tseng Species: Sapium sebiferum (L.) Roxb. S. discolor (Champ. ex Benth.) (=Triadica sebifera (L.) Small) S. rotundifolium Hemsl. Muell. Arg. Description Sapium sebiferum is a deciduous tree The petiole is slender, 2.5-6 cm long, the inflorescence. The female flower is that can reach 15 m in height. Most bearing 2 glands in the terminal. The borne on the pedicel, which is 2-4 mm parts of the plant are glabrous. The bark stem contains a milky, poisonous sap. long with 2 kidney-shaped glands in is gray to whitish-gray with vertical Flowers are monoecious, without petals the base. The flowers appear from April cracks. The alternate leaves are broad or flower discs, arranged as terminal through August. Fruits are pear-shaped rhombic to ovate 3-8 cm long and 3-8 spikes. The slender male flowers have globular capsules 1-1.5 cm in diameter. cm wide, entire margin, and a cordate- a 3-lobed cuplike calyx and 2 stamens Each fruit contains 3 black seeds that acuminate apex and a rounded base. -
Steinernema Glaseri Against the Moringa Hairy Caterpillar, Eupterote Mollifera
04 Subramanian_149 22-12-2005 15:21 Pagina 149 Nematol. medit. (2005), 33: 149-155 149 1THE INFECTIVITY OF THE ENTOMOPATHOGENIC NEMATODE, STEINERNEMA GLASERI AGAINST THE MORINGA HAIRY CATERPILLAR, EUPTEROTE MOLLIFERA S. Subramanian¥, R. Parthasarathy¥, R.J. Rabindra#, N. Sathiah¥ and S. Rajagopal Babu¥ ¥ Department of Agricultural Entomology, Tamil Nadu Agricultural University, Coimbatore-641 003, India # Project Directorate of Biological Control (ICAR), Bangalore-560 025, India Summary. The entomopathogenic nematode, Steinernema glaseri was tested against the Moringa hairy caterpillar, Eupterote mol- lifera in laboratory investigations. It was highly effective against third, fourth and fifth instars of E. mollifera with LC50 and LT50 in the range of 16.5-24.1 infective juveniles (IJ) per larva and 50.3-69.7 h, respectively. The mortality rate decreased with increase in age of the larvae. Penetration of IJ was less in E. mollifera larvae (18-56%) than in Galleria mellonella larvae (45-85%) but pene- tration of both species differed significantly with the number of IJ applied and the age of the larvae. The yield of IJ per larva was significantly less (0.11-0.21 × 105 per g of larva) in E. mollifera than in G. mellonella (2.75-3.87 × 105 per g of larva). Spray applica- tion of IJ of S. glaseri at a concentration of 1000 IJ per 10 ml was found to be effective, with a mortality of 83.3% of fourth instar larvae of E. mollifera. Entomopathogenic nematodes (EPN) belonging to and soap industry (Ramachandran et al., 1980; Nautiyal the family Steinernematidae have been recognized as ef- and Venkataraman, 1987), tender shoots, buds, flowers fective insect control agents (Poinar, 1990). -
Lepidoptera) of Vietnam
HỘI NGHỊ KHOA HỌC TOÀN QUỐC VỀ SINH THÁI VÀ TÀI NGUYÊN SINH VẬT LẦN THỨ 4 A PRELIMINARY LIST OF THE EUPTEROTIDAE (LEPIDOPTERA) OF VIETNAM SERGEY N. PUGAEV Ulyanovsk State Pedagogical University TRAN THIEU DU Institute of Ecology and Biological Resource The family Eupterotidae contains about 60 genera, the majority of them occurring in the tropics. The classification and phylogeny of the group remains inadequately studied, and the family has never been properly and fully catalogued, having been omitted from Junk’s Lepidopterorum Catalogus. Only Forbes (1955) published a systematic checklist of the world genera, which is somewhat incomplete and now partly out of date, and Nässig & Oberprieler (2008) produced a modern catalogue based on original point of view on score of most genera. They also clarified the nomenclature of the family-group names in Eupterotidae (Nässig & Oberprieler 2007), and this catalogue was used with changes for preparing of the present paper. The first species of the Eupterotidae described from Vietnam was Pseudojana vitalisi Candèze, 1927 that pointed from Indochina. The generic attribution was obviousely wrong but the type of the species has not been found so far and tentavily the taxon is placed into the genus Eupterote Hübner,1820. To date, no one work was devoted specially to Vietnamese Eupterotidae, and only in the articles of L. Candèze (1927), J. de Joannis (1929) and A. Lemée (1950) we found information and short lists of species mostly faulty identified. Some species were listed recently by vietnamese colleagues as defoliators: Plant Protection Research Institute (1976) and Tran Thieu Du (2009). -
Macro Moths of Tinsukia District, Assam: a JEZS 2017; 5(6): 1612-1621 © 2017 JEZS Provisional Inventory Received: 10-09-2017 Accepted: 11-10-2017
Journal of Entomology and Zoology Studies 2017; 5(6): 1612-1621 E-ISSN: 2320-7078 P-ISSN: 2349-6800 Macro moths of Tinsukia district, Assam: A JEZS 2017; 5(6): 1612-1621 © 2017 JEZS provisional inventory Received: 10-09-2017 Accepted: 11-10-2017 Subhasish Arandhara Subhasish Arandhara, Suman Barman, Rubul Tanti and Abhijit Boruah Upor Ubon Village, Kakopather, Tinsukia, Assam, India Abstract Suman Barman This list reports 333 macro moth species for the Tinsukia district of Assam, India. The moths were Department of Wildlife Sciences, captured by light trapping as well as by opportunistic sighting across 37 sites in the district for a period of Gauhati University, Assam, three years from 2013-2016. Identification was based on material and visual examination of the samples India with relevant literature and online databases. The list includes the family, subfamily, tribes, scientific name, the author and year of publication of description for each identified species. 60 species in this Rubul Tanti inventory remain confirmed up to genus. Department of Wildlife Biology, A.V.C. College, Tamil Nadu, Keywords: Macro moths, inventory, Lepidoptera, Tinsukia, Assam India Introduction Abhijit Boruah Upor Ubon Village, Kakopather, The order Lepidoptera, a major group of plant-eating insects and thus, from the agricultural Tinsukia, Assam, India and forestry point of view they are of immense importance [1]. About 134 families comprising 157, 000 species of living Lepidoptera, including the butterflies has been documented globally [2], holding around 17% of the world's known insect fauna. Estimates, however, suggest more species in the order [3]. Naturalists for convenience categorised moths into two informal groups, the macro moths having larger physical size and recency in evolution and micro moths [4] that are smaller in size and primitive in origin . -
Status of Insect Pests of Poplar in India with Special Reference to Clostera Spp
Status of Insect Pests of Poplar in India with Special Reference to Clostera spp. Mukhtar Ahmad and Mohammad Faisal Forest Entomology Division, Forest Research Institute, Dehradun – 248 006 Introduction ost of the exotic poplars, especially Populus deltoides have been suffering multiple insect injuries since their introduction in India. MInfestation by different insect species to poplar has been reported from time to time by many workers, including Pruthi and Batra (1960); Chatterjee and Thapa (1964); Seth (1969); Lohani (1976); Chatterjee and Chaturvedi (1981); Singh et al. (1983); Singh and Prasad (1985); Singh and Singh (1986); Sohi (1989), etc. Such reports provide specific information of insect incidences. Large scale defoliation of P. deltoides trial plantations (Clones G-3 and G-48, IC-100, 3-4 yrs of age) by Clostera cupreta (Butler) and C. fulgurita (Walker) was reported from time to time from the Central Tarai region of Uttar Pradesh (Seth, 1969; Lohani, 1976; Chaturvedi, 1981; Singh et al., 1983) . By 1980s, the defoliation outbreak spread over an area of 1,100 ha and became alarming. It had to be supressed by aerial spraying of carbaryl (Sevin) insecticide (Singh et al., 1983; Singh, 1998). This defoliator has now spread through out the region of P. deltoides growing. Large scale defoliation by Clostera spp. is known to significantly decrease the growth increment of poplar trees (Gao et al., 1985). Severe and repeated defoliation in young plants results in mortality (Singh and Singh, 1986). Severe attack by Apriona cinerea Chevrolat (poplar stem borer) was reported in 2-3 yrs old P. deltoides plantations, from Paonta Valley in Himachal Pradesh (Verma and Khurana, 1985); Jammu region (Sharma and Bhatia, 1996) and also from other parts of Uttar Pradesh and Haryana (Singh et al., 1987). -
Antibacterial Activity of Immune Hemolymph from a Natural Diet Rearing Eupterote Mollifera Larvae
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 05 Issue: 04 | Apr-2018 www.irjet.net p-ISSN: 2395-0072 ANTIBACTERIAL ACTIVITY OF IMMUNE HEMOLYMPH FROM A NATURAL DIET REARING EUPTEROTE MOLLIFERA LARVAE Agilandeswari Vinoth Assistant Professor, Department of Biotechnology, Vivekanandha College of Engineering for Women, Tamilnadu, India. ----------------------------------------------------------------------***------------------------------------------------------------------- ABSTRACT - A Natural diet and rearing system was standardized for Eupterote Mollifera under natural environmental conditions. Larvae of the moth Eupterote Mollifera were reared on a natural diet of moringa oleifera leaves. The last instar larvae were reared till the larvae were formed into moth. And third and fourth instar larvae were immune-challenged by an injection of live Escherichia Coli D31. Hemolymph were collected from the larvae and prepared hemocyte free hemolymph by centrifugation process. The extra cellular protein/peptide was concentrated by AMICON (MWCO-3kDa) ultra-centrifugal filters. The protein concentration was estimated by Bradford dye binding assay. The Antibacterial activity of purified hemolymph was tested against Gram-positive, Gram-negative bacteria of B.subtilis, E-coli, S.aureus, K.pnemoniae by well diffusion assay and colony counting assay using Escherichia Coli, final average CFU values of two different samples (>3kDa and <3kDa) were calculated by two different dilution ratio. Keywords: Natural diet, rearing, Eupterote Mollifera, immune-challenge, Hemolymph, CFU, Antibacterial INTRODUCTION Insects play many important roles in nature. They aid bacteria, fungi, and other organisms in the decomposition of organic matter and in soil formation. The decay of carrion, for example, brought about mainly by bacteria, is accelerated by the maggots of flesh flies and blowflies. -
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. -
Phylogenomics Reveals the Evolutionary Timing and Pattern of Butterflies and Moths
Phylogenomics reveals the evolutionary timing and pattern of butterflies and moths Akito Y. Kawaharaa,1, David Plotkina,b, Marianne Espelanda,c, Karen Meusemannd,e,f, Emmanuel F. A. Toussainta,g, Alexander Donathe, France Gimniche, Paul B. Frandsenh,i, Andreas Zwickf, Mario dos Reisj, Jesse R. Barberk, Ralph S. Petersc, Shanlin Liul,m, Xin Zhoum, Christoph Mayere, Lars Podsiadlowskie, Caroline Storera, Jayne E. Yackn, Bernhard Misofe, and Jesse W. Breinholta,o,2 aMcGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611; bEntomology and Nematology Department, University of Florida, Gainesville, FL 32611; cArthropoda Department, Alexander Koenig Zoological Research Museum, D-53113 Bonn, Germany; dDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, D-79104 Freiburg, Germany; eCenter for Molecular Biodiversity Research, Alexander Koenig Zoological Research Museum, D-53113 Bonn, Germany; fAustralian National Insect Collection, National Research Collections Australia, Commonwealth Scientific and Industrial Research Organisation, Canberra, Acton, ACT 2601, Australia; gDepartment of Entomology, Natural History Museum of Geneva, 1208 Geneva, Switzerland; hPlant and Wildlife Sciences, Brigham Young University, Provo, UT 84602; iData Science Lab, Smithsonian Institution, Washington, DC 20002; jSchool of Biological and Chemical Sciences, Queen Mary University of London, London E1 4NS, United Kingdom; kDepartment of Biological