2 Life Table Studies of Trilocha Virescence
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ILLUSTRATIONS of MOTHS in TAIWAN, 1-5 by B. S. Chang
142 BOOK REVIEW TROPICAL LEPIDOPTERJ Tropical Lepidoptera, 4(2): 142 BOOK REVIEW ILLUSTRATIONS OF MOTHS IN TAIWAN, 1-5 by B. S. Chang Vol. 1: Sphingidae, Ratardidae. Epipyropidae, Drepanidae, Cyclidiidae, Thyatiridae, Epicopeiidae, Callidulidae. Lasiocampidae. EupterotidJ Bombycidae, Brahmaeidae, Agaristidae [Noctuidae, part]. 242 pp, 271 col. fig., col. cover. 1989. (paper only) Vol. 2: Arctiidae, Hypsidae [Noctuidae, part], Limacodidae, Notodontidae. 310 pp, 356 col. fig., col. cover. 1989. Vol. 3: Geometridae [1]. Oenochrominae, Geometrinae, Sterrhinae, Larentiinae. 350 pp, 405 col. fig., col. cover. 1989. Vol. 4: Geometridae [2]. Ennominae. 480 pp, 684 col. fig., col. cover. 1990. Vol. 5: Noctuidae [1]. 366 pp. 572 col. fig., col. cover. 1991. (paper only) 1989-91. Taiwan Museum, Taipei. All are 21 x 18.5 cm. (elongate) In Chinese; Latin names. Price for each is S35.00 paper, S42.00 cloth. Available from Flora & Fauna Books, P. O. Box 15718, Gainesville, FL 32604 (plus S2 shipping each, or 55 per set). This series of small, full-color books is the result of a lifetime of with 706 species illustrated out of the 791 recorded for Taiwan. TlJ collecting by retired Taiwan high school teacher B. S. Chang. Until color figures are all excellent but many of the wing venation drawing 1991, 5 volumes were completed, but the second part of the Noctuidae are very faintly reproduced in the books. has unfortunately been halted by the untimely death of the author. It is Overall, the books are one of the unique treatments of Lepidoptera ii not known if a manuscript is available for the eventual completion of the world. -
Bombyx Mori L.) and Wild Silkworm (Bombyx Mandarina M.) to Phoxim Insecticide
African Journal of Biotechnology Vol. 9(12), pp. 1771-1775, 22 March, 2010 Available online at http://www.academicjournals.org/AJB ISSN 1684–5315 © 2010 Academic Journals Full Length Research Paper Resistance comparison of domesticated silkworm (Bombyx mori L.) and wild silkworm (Bombyx mandarina M.) to phoxim insecticide Bing Li1,2, Yanhong Wang2, Haitao Liu2, YaXiang Xu1,2, Zhengguo Wei1,2, YuHua Chen1,2 and Weide Shen1,2 1National Engineering Laboratory for Modern Silk, Soochow University 215123, Suzhou, China. 2School of Basic Medicine and Biological Sciences, Soochow University 215123, Suzhou, China. Accepted 11 March, 2010 In this study, the resistance difference to phoxim between Bombyx mori L. and Bombyx mandarina M was investigated. For the both silkworm species, the whole body of each larval were collected, and on the third day of the 5th instar, the brain, midgut, fat bodies, and silk gland were collected for enzymatic activity assay of acetylcholinesterase (AChE). Our results showed that in the early larval stages, the resistance difference to phoxim was not significant between the two species. However, in the 4th and 5th instar, the resistance differences showed significant increase. When compared to B. mori L, the LC50 of B. mandarina was 4.43 and 4.02-fold higher in the 4th and 5th instar, respectively. From the 1st to 5th instar, the enzymatic activities of AChE of B. mandarina were 1.60, 1.65, 1.81, 1.93 and 2.28-fold higher than that of B. mori, respectively. For the brain, midgut, fat body, and silk gland on the third day of the 5th instar, the enzymatic activity ratios of B. -
Influence of Habitat and Bat Activity on Moth Community Composition and Seasonal Phenology Across Habitat Types
INFLUENCE OF HABITAT AND BAT ACTIVITY ON MOTH COMMUNITY COMPOSITION AND SEASONAL PHENOLOGY ACROSS HABITAT TYPES BY MATTHEW SAFFORD THESIS Submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology in the Graduate College of the University of Illinois at Urbana-Champaign, 2018 Urbana, Illinois Advisor: Assistant Professor Alexandra Harmon-Threatt, Chair and Director of Research ABSTRACT Understanding the factors that influence moth diversity and abundance is important for monitoring moth biodiversity and developing conservation strategies. Studies of moth habitat use have primarily focused on access to host plants used by specific moth species. How vegetation structure influences moth communities within and between habitats and mediates the activity of insectivorous bats is understudied. Previous research into the impact of bat activity on moths has primarily focused on interactions in a single habitat type or a single moth species of interest, leaving a large knowledge gap on how habitat structure and bat activity influence the composition of moth communities across habitat types. I conducted monthly surveys at sites in two habitat types, restoration prairie and forest. Moths were collected using black light bucket traps and identified to species. Bat echolocation calls were recorded using ultrasonic detectors and classified into phonic groups to understand how moth community responds to the presence of these predators. Plant diversity and habitat structure variables, including tree diameter at breast height, ground cover, and vegetation height were measured during summer surveys to document how differences in habitat structure between and within habitats influences moth diversity. I found that moth communities vary significantly between habitat types. -
Lepidoptera: Noctuoidea: Erebidae) and Its Phylogenetic Implications
EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 113: 558–570, 2016 http://www.eje.cz doi: 10.14411/eje.2016.076 ORIGINAL ARTICLE Characterization of the complete mitochondrial genome of Spilarctia robusta (Lepidoptera: Noctuoidea: Erebidae) and its phylogenetic implications YU SUN, SEN TIAN, CEN QIAN, YU-XUAN SUN, MUHAMMAD N. ABBAS, SAIMA KAUSAR, LEI WANG, GUOQING WEI, BAO-JIAN ZHU * and CHAO-LIANG LIU * College of Life Sciences, Anhui Agricultural University, 130 Changjiang West Road, Hefei, 230036, China; e-mails: [email protected] (Y. Sun), [email protected] (S. Tian), [email protected] (C. Qian), [email protected] (Y.-X. Sun), [email protected] (M.-N. Abbas), [email protected] (S. Kausar), [email protected] (L. Wang), [email protected] (G.-Q. Wei), [email protected] (B.-J. Zhu), [email protected] (C.-L. Liu) Key words. Lepidoptera, Noctuoidea, Erebidae, Spilarctia robusta, phylogenetic analyses, mitogenome, evolution, gene rearrangement Abstract. The complete mitochondrial genome (mitogenome) of Spilarctia robusta (Lepidoptera: Noctuoidea: Erebidae) was se- quenced and analyzed. The circular mitogenome is made up of 15,447 base pairs (bp). It contains a set of 37 genes, with the gene complement and order similar to that of other lepidopterans. The 12 protein coding genes (PCGs) have a typical mitochondrial start codon (ATN codons), whereas cytochrome c oxidase subunit 1 (cox1) gene utilizes unusually the CAG codon as documented for other lepidopteran mitogenomes. Four of the 13 PCGs have incomplete termination codons, the cox1, nad4 and nad6 with a single T, but cox2 has TA. It comprises six major intergenic spacers, with the exception of the A+T-rich region, spanning at least 10 bp in the mitogenome. -
Scholars Academic Journal of Biosciences
Scholars Academic Journal of Biosciences Abbreviated Key Title: Sch Acad J Biosci ISSN 2347-9515 (Print) | ISSN 2321-6883 (Online) Biology of Plant Diseases Journal homepage: https://saspublishers.com Life Table of Trilocha varians (Lepidoptera: Bombycidae) on Ficus benjamina Under Laboratory Conditions Muhammad Ramzan1*, Ghulam Murtaza2, Iram Abbas3, Muhammad Numan khan4, Rabia khan5, Ghulam Mustafa6, Muhammad Shoaib3 1State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China 2Department of Entomology, College of Plant Protection, China Agricultural University, Beijing, China 3Department of Zoology wildlife and fisheries, University of Agriculture, Faisalabad, Pakistan 4Department of Zoology, Faculty of biological sciences, Quaid-i-Azam University, Islamabad, Pakistan 5University of Agriculture, CABB, Biotechnology, Faisalabad, Pakistan 6Department of Entomology, University of Agriculture Faisalabad, Pakistan DOI: 10.36347/sajb.2021.v09i06.001 | Received: 18.04.2021 | Accepted: 03.06.2021 | Published: 06.06.2021 *Corresponding author: Muhammad Ramzan Abstract Original Research Article Ficus benjamina is an ornamental plant that planted alongside the road of Pakistan to increase the beauty of country. Several insect pests are attacking on this beautiful plant, responsible in reduction of aesthetic value of country. Among insect pests, Trilocha varians is serious and destructive pest whose larvae feed on leaves resulting 100% defoliation. The study was conducted to check the life table of this emerging pest on F. benjamina under controlled conditions. The study showed that total life period of T. varians from egg to adult was 33-35 days. The highest apparent mortality was recorded in early larval instars and rapidly reduced in later instars (3rd instars) which even reached to zero from 4th larval instars to pupal stage. -
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. -
1 Evolution of Sexual Development and Sexual Dimorphism in Insects 1
1 Evolution of sexual development and sexual dimorphism in insects 2 3 Ben R. Hopkins1* & Artyom Kopp1 4 5 1. Department of Evolution and Ecology, University of California – Davis, Davis, USA 6 7 * Corresponding author 8 9 Corresponding author email: [email protected] 10 11 12 13 14 Abstract 15 Most animal species consist of two distinct sexes. At the morphological, physiological, and 16 behavioural levels the differences between males and females are numerous and dramatic, yet 17 at the genomic level they are often slight or absent. This disconnect is overcome because simple 18 genetic differences or environmental signals are able to direct the sex-specific expression of a 19 shared genome. A canonical picture of how this process works in insects emerged from decades 20 of work on Drosophila. But recent years have seen an explosion of molecular-genetic and 21 developmental work on a broad range of insects. Drawing these studies together, we describe 22 the evolution of sexual dimorphism from a comparative perspective and argue that insect sex 23 determination and differentiation systems are composites of rapidly evolving and highly 24 conserved elements. 25 1 26 Introduction 27 Anisogamy is the definitive sex difference. The bimodality in gamete size it describes 28 represents the starting point of a cascade of evolutionary pressures that have generated 29 remarkable divergence in the morphology, physiology, and behaviour of the sexes [1]. But 30 sexual dimorphism presents a paradox: how can a genome largely shared between the sexes 31 give rise to such different forms? A powerful resolution is via sex-specific expression of shared 32 genes. -
The Sex Determination Cascade in the Silkworm
G C A T T A C G G C A T genes Review The Sex Determination Cascade in the Silkworm Xu Yang 1,2, Kai Chen 1,2, Yaohui Wang 1, Dehong Yang 1,2 and Yongping Huang 1,* 1 Key Laboratory of Insect Developmental and Evolutionary Biology, Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai 200032, China; [email protected] (X.Y.); [email protected] (K.C.); [email protected] (Y.W.); [email protected] (D.Y.) 2 University of Chinese Academy of Sciences, Beijing 100049, China * Correspondence: [email protected] Abstract: In insects, sex determination pathways involve three levels of master regulators: primary signals, which determine the sex; executors, which control sex-specific differentiation of tissues and organs; and transducers, which link the primary signals to the executors. The primary signals differ widely among insect species. In Diptera alone, several unrelated primary sex determiners have been identified. However, the doublesex (dsx) gene is highly conserved as the executor component across multiple insect orders. The transducer level shows an intermediate level of conservation. In many, but not all examined insects, a key transducer role is performed by transformer (tra), which controls sex-specific splicing of dsx. In Lepidoptera, studies of sex determination have focused on the lepidopteran model species Bombyx mori (the silkworm). In B. mori, the primary signal of sex determination cascade starts from Fem, a female-specific PIWI-interacting RNA, and its targeting gene Masc, which is apparently specific to and conserved among Lepidoptera. -
The Effect of Temperature on the Development of Trilocha Varians (Lepidoptera: Bombycidae) and Control of the Ficus Plant Pest
Tropical Life Sciences Research, 30(1), 23–31, 2019 The Effect of Temperature on the Development of Trilocha varians (Lepidoptera: Bombycidae) and Control of the Ficus Plant Pest 1Norasmah Basari*, 1Nurul Salsabila Mustafa, 1Nur Elya Nabila Yusrihan, 1Chin Wei Yean and 2Zainal Ibrahim 1School of Marine and Environmental Sciences, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia 2Majlis Bandaraya Kuala Terengganu, Menara Permint, Jalan Sultan Ismail, 21000 Kuala Terengganu, Terengganu, Malaysia Published date: 31 January 2019 To cite this article: Norasmah Basari, Nurul Salsabila Mustafa, Nur Elya Nabila Yusrihan, Chin Wei Yean and Zainal Ibrahim. (2019). The effect of temperature on the development of Trilocha varians (lepidoptera: bombycidae) and control of the ficus plant pest. Tropical Life Sciences Research 30(1): 23–31. https://doi.org/10.21315/tlsr2019.30.1.2 To link to this article: https://doi.org/10.21315/tlsr2019.30.1.2 Abstrak: Pokok Ficus biasa ditanam sebagai tanaman hiasan di sepanjang jalan raya di Malaysia. Pada tahun 2010, pokok Ficus di Kuala Terengganu didapati telah diserang oleh kupu-kupu yang dikenali sebagai Trilocha varians. Larva kupu-kupu pemakan daun ini boleh menyebabkan pokok Ficus mengalami kehilangan daun sehingga 100%. Kajian ini dijalankan untuk menentukan kitar hidup T. varians di bawah dua suhu persekitaran yang berbeza dan untuk mengawal serangga perosak ini menggunakan dua jenis insektisid. Keputusan menunjukkan terdapat perbezaan yang signifikan bagi masa yang diambil untuk telur menetas dan jangka masa bagi larva dan pupa di antara suhu persekitaran rendah dan tinggi. Keputusan juga menunjukkan fipronil mempunyai LT50 dan LT95 yang rendah berbanding malathion. Kajian ini memberi maklumat baharu berkaitan kitar hidup T. -
Two Dopamine D2-Like Receptor Genes from the Silkworm
www.nature.com/scientificreports OPEN Two dopamine D2-like receptor genes from the silkworm (Bombyx mori) and their evolutionary history Received: 8 November 2016 Accepted: 9 June 2017 in metazoan Published online: 28 July 2017 Ping Chen, Peng Chen, Tian Li, Qi Shen, Deng-Feng Yan, Liang Zhang, Xi Chen, Yan Li & Wei Zhao Dopamine is widely distributed in metazoans and is implicated in many physiological functions. Dopaminergic signaling is mediated through two classes of dopamine receptors, D1-like and D2-like. Phylogeny analysis reveals that, the dopamine receptors probably appeared ahead of the cnidarian divergence, two distinct classes of dopamine receptors likely formed prior to the separation of deuterostomes and protostomes, and INDRs probably split from its ancestor before the emergence of nematodes. Two D2-like genes are closely linked on the same scafold, and the chromosome region around D2-like gene loci show colinearity among diferent species within Lepidoptera. These indicate two D2-like and their adjunction genes are likely Lepidoptera-specifc orthologs, and occur by gene duplication event taken place after Lepidoptera ancestor split from the common ancestor of Lepidoptera and Diptera. In silkworm, two D2-like genes were expressed in examined tissues, and encoded BmDop2R2 having all the features of D2-like receptors and BmDop2R1 being a truncated variant without the region of N-terminal to TM II. Only dopamine distinctly lowered cAMP levels in BmDop2R2-expressing cells, whereas all tested amines for BmDop2R1 had not markedly efect in pharmacological test. These suggest there is functional diference between the two genes, which are likely resulted from subfunctionalization of gene duplication. -
Mitochondrial Genomes of Two Bombycoidea Insects and Implications for Their Phylogeny
www.nature.com/scientificreports OPEN Mitochondrial Genomes of Two Bombycoidea Insects and Implications for Their Phylogeny Received: 20 February 2017 Zhao-Zhe Xin, Yu Liu, Xiao-Yu Zhu, Ying Wang, Hua-Bin Zhang, Dai-Zhen Zhang, Chun-Lin Accepted: 22 June 2017 Zhou, Bo-Ping Tang & Qiu-Ning Liu Published online: 26 July 2017 The mitochondrial genome (mt genome) provides important information for understanding molecular evolution and phylogenetics. As such, the two complete mt genomes of Ampelophaga rubiginosa and Rondotia menciana were sequenced and annotated. The two circular genomes of A. rubiginosa and R. menciana are 15,282 and 15,636 bp long, respectively, including 13 protein-coding genes (PCGs), two rRNA genes, 22 tRNA genes and an A + T-rich region. The nucleotide composition of the A. rubiginosa mt genome is A + T rich (81.5%) but is lower than that of R. menciana (82.2%). The AT skew is slightly positive and the GC skew is negative in these two mt genomes. Except for cox1, which started with CGA, all other 12PCGs started with ATN codons. The A + T-rich regions of A. rubiginosa and R. menciana were 399 bp and 604 bp long and consist of several features common to Bombycoidea insects. The order and orientation of A. rubiginosa and R. menciana mitogenomes with the order trnM-trnI-trnQ-nad2 is diferent from the ancestral insects in which trnM is located between trnQ and nad2 (trnI-trnQ-trnM- nad2). Phylogenetic analyses indicate that A. rubiginosa belongs in the Sphingidae family, and R. menciana belongs in the Bombycidae family. -
As Pest of Jackfruit and Some Ornamental Species of Ficus in the Philippines
J. ISSAAS Vol. 19, No. 2:41-48 (2013) OCCURRENCE OF THE MORACEAE-FEEDING BOMBYCID, Trilocha varians (Walker) (BOMBYCIDAE, LEPIDOPTERA) AS PEST OF JACKFRUIT AND SOME ORNAMENTAL SPECIES OF FICUS IN THE PHILIPPINES Mario V. Navasero, Marcela M. Navasero, Maureen Ceres dL. de Roxas and Susan May F. Calumpang National Crop Protection Center, Crop Protection Cluster, College of Agriculture, University of the Philippines Los Baños, College, Laguna, Philippines 4031 Corresponding author: [email protected] (Received: August 15, 2013; Accepted: November 8, 2013 ) ABSTRACT The occurrence of the bombycid moth, Trilocha varians (Walker) (Lepidoptera: Bombycidae) was observed and monitored among Ficus benjamina and F. nitida in the landscape of the National Crop Protection Center from August to December 2012. Eggs, larvae and pupae of the pest were all present on the infested shrubs. The larvae completely defoliated and eventually killed some of the Ficus plants . At the peak of infestation, larvae can consume all of the leaves of an individual shrub in just overnight. T. varians was also observed infesting jackfruit in Los Baños, Laguna and Balete, Batangas as well as on F. nitida in Baguio City . The nature of damage, host response and host range were discussed. This is the first record of T. varians as pest of Artocarpus heterpphyllus, A. communis , A. kamansi and some ornamental species of Ficu s in the Philippines. Key words: damage, host range, invasive pest INTRODUCTION The Philippines for the last several years was affected by outbreaks and isolated serious infestations of invasive pest species - Stenocranus pacificus Kirkaldy on corn, Nipaecocus nipae (Maskell), Brontispa longissima Gestro, and Aspidiotus sp., a species of scale insect, all on coconut, as well as native species like Spodoptera exempta (Walker) on graminaceous crops and weeds.