2 Life Table Studies of Trilocha Virescence
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2 Life Table Studies of Trilocha Virescence
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Directory of Open Access Journals Asian J Agri Biol, 2013, 1(1):2-7. LIFE TABLE STUDIES OF TRILOCHA VIRESCENCE (BOMBYCIDAE: LEPIDOPTERA) ON FICUS NITIDA Muhammad Asif Aziz 1, Ayesha Iftkhar 1 and Muhammad Hanif 2 1Department of Entomology, PMAS-Arid Agriculture University Rawalpindi, Pakistan 2Department of Mathematics and Statistics, PMAS-Arid Agriculture University Rawalpindi, Pakistan ABSTRACT The life table of Trilocha virescence was constructed in the laboratory which is a serious Lepidopterous pest of Ficus nitida . The study declared different impact of larval and adult mortality on the population. Pre reproductive mortality was 30% and 70 percent of the individuals’ survived up to the maturity and took part in reproduction. Larval mortality was greater in 1 st instar than all other stages. No mortality was observed in 4 th and 5 th larval instar in subsequent stages. High mortality during 1 st instar may exert significant negative effect on the insect population and may be best used for applying control tactics. The net reproductive rate of the insect was 45.44 per individual per generation. Keywords: Trilocha virescence , stage specific, cohort, life table, life expectancy, mortality rate, survivorship INTRODUCTION revealing the maximal growth potential of a population (Gabre et al, 2004). Life tables used Computing life tables is a fairly current can make quantitatively and qualitatively approach used by entomologists to study the evaluation of various host plants insects’ population dynamics. With the recent (Ambegaonkar and Bilapate, 1981). emphasis on population dynamic studies of Two kinds of life tables have been developed: insects, the usefulness of life table in this area (1). -
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. -
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. -
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. -
Revision Der Orientalischen Bombycidae Von Wolfgang Dierl
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Spixiana, Zeitschrift für Zoologie Jahr/Year: 1977 Band/Volume: 001 Autor(en)/Author(s): Dierl Wolfgang Artikel/Article: Revision der orientalischen Bombycidae (Lepidoptera) Teil I: Die Ocinara-Gruppe 225-268 ©Zoologische Staatssammlung München;download: http://www.biodiversitylibrary.org/; www.biologiezentrum.at Spixiana 225—268 München, 15. Dez. 1978 ISSN 0341-8391 Revision der orientalischen Bombycidae (Lepidoptera) Teil I: Die Ocinara-Gruppe Von Wolfgang Dierl Zoologische Staatssammlung München Abstract All the 31 known taxa of the generic group Ocinara from the Oriental region are dealt with in this paper. 22 species are described and figured, including 6 new genera, 7 new species and 2 new subspecies. The remaining taxa are synonymic names. The descriptions are mainly based on external and genitalic characters of the imago, partly on larval struc- tures. An account is given on the morphology, phylogeny and zoogeography of the group including the description of some very specialized structures in the male genitalia which probably are functioning as odorific organs. 1. Einleitung Während unserer Nepal-Expeditionen der Jahre 1962, 1964, 1967 und 1973 konnte eine kleine Anzahl von Exemplaren aus der Ocinara-Gruppe gesammelt werden. Die Bestimmung dieses Materials, basierend auf der üblichen Untersuchung der äußeren und inneren Merkmale, erbrachte ein überraschend unklares Ergebnis, das nach einer Revision der Gruppe rief. Es zeigte sich nämlich, daß nicht nur die Arten ungenügend definiert waren, sondern auch die Gattungszugehörigkeit in den meisten Fällen falsch war. So wurden nun die Typen der beschriebenen Taxa unter- sucht und die Ergebnisse führten zu einer völlig neuen Gruppierung mit Beschrei- bung neuer Gattungen und Arten. -
Embryo Development and Sex Determination in the Cassava Whitefly (Bemisia Tabaci)
Embryo development and sex determination in the Cassava whitefly (Bemisia tabaci) Rebecca Louise Corkill University of East Anglia A thesis submitted for the degree of Doctor of Philosophy September 2019 This copy of the thesis has been supplied on condition that anyone who consults it is understood to recognise that its copyright rests with the author and that use of any information derived there from must be in accordance with current UK Copyright law. In addition, any quotation or extract must include full attribution. Abstract The cassava whitefly, Bemisia tabaci (Hemiptera: Aleyrodidae), is a highly invasive and destructive agricultural pest, with a global distribution. B. tabaci insect has evolved resistance to multiple insecticides, and therefore, new control methods will have to be developed to control this insect. The self-limiting system, which produces a female-specific lethal heritable element and causes population suppression, works well for control of mosquitoes. The goal of this thesis is to assess the feasibility of creating a self-limiting system in B. tabaci. The self-limiting system requires generating transgenic insects, and this is done via injection of constructs into eggs at the pre-germ-line cell stage (around blastoderm formation), this enables stable germline transformation. However, there has been limited research into B. tabaci early embryogenesis stages, and therefore it is unclear when transformation constructs will have to be introduced. In this thesis, I conducted confocal microscopy studies to determine the timing of early embryogenesis stages in B. tabaci MED. Unexpectedly, I revealed that early embryogenesis in B. tabaci starts before the eggs are oviposited, unlike in mosquitoes and fruitflies. -
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. -
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 . -
Effect of Temperature on the Life Cycle of Trilocha Varians (Lepidoptera: Bombycidae) in Pakistan
Pure Appl. Biol., 9(1): 436-442, March, 2020 http://dx.doi.org/10.19045/bspab.2020.90047 Research Article Effect of temperature on the life cycle of Trilocha varians (Lepidoptera: Bombycidae) in Pakistan Muhammad Ramzan, Unsar Naeem-Ullah*, Naeem Iqbal, Zartasha Rasheed, Shafia Saba, Hafsah Ghaffar and Shafqat Saeed Institute of Plant Protection, MNS-University of Agriculture Multan, Punjab-Pakistan *Corresponding author’s email: [email protected] Citation Muhammad Ramzan, Unsar Naeem-Ullah, Naeem Iqbal, Zartasha Rasheed, Shafia Saba, Hafsah Ghaffar and Shafqat Saeed. Effect of temperature on the life cycle of Trilocha varians (Lepidoptera: Bombycidae) in Pakistan. Pure and Applied Biology. Vol. 9, Issue 1, pp436-442. http://dx.doi.org/10.19045/bspab.2020.90047 Received: 06/08/2019 Revised: 22/10/2019 Accepted: 08/11/2019 Online First: 13/11/2019 Abstract Ficus benjamina is known as weeping fig, planted along roadsides in Pakistan to increase the aesthetic value of the country. It is native to tropical and sub-tropical regions of the world. In 2019, plants were infested by leaf eating caterpillar, identified as Trilocha varians. The larvae of the pest were caused up to 100% defoliation of F. benjamina. The aim of the recent study was to determine the life cycle of T. varians under two different environmental temperatures i.e. 26°C ± 1.0 controlled and uncontrolled 33°C ±2.0. The recent study was obtained that there was significant difference in the time taken for eggs, larval and pupal period of T. varians between high and low environmental temperatures. The life cycle of the test insect, T. -
Observation on Trilocha Varains (Lepidoptera: Bombycidae)
International Journal of Agricultural Technology 2017 Vol. 13(7.3): 2189-2195 Available online http://www.ijat-aatsea.com ISSN 1686-9141 Observation on Trilocha varians (Lepidoptera: Bombycidae) Sawitri Chuenban1, S. Bumroongsook1* and S. Tigvattananont2 1Department of Plant Production Technology, Faculty of Agricultural Technology, King Mongkut‘s Institute of Technology Ladkrabang, Bangkok 10520, Thailand; 217 Ngamwongvan Rd., Thasai Subdistrict, Muang District, Nonthaburi, Thailand. Chuenban S., S. Bumroongsook and S. Tigvattananont. (2017). Observation on Trilocha varains (Lepidoptera: Bombycidae). International Journal of Agricultural Technology 13(7.3): 2189-2195. Biological studies of the silkworm larvae in the laboratory revealed that after mating, females laid eggs in consecutive rows, sometimes observed 2-6 layers. These eggs were often found attached to the side of plastic rearing cup or its lid 2-15 eggs/group. Innature, the female usually lay eggs on the dorsal part of the fig leaves, 3-24 eggs/group. The female can lay eggs between 160-270 eggs, whereas the unmated adults can lay 15-183 eggs /insect. These unfertilized eggs would not developed into larvae. Egg incubation period was 3.33-3.62 days. The developmental time for larval instar 1- 5 was 1.97 ± 0.09, 2.00 ± 0.06, 2.03 ± 0.05, 2.12 ± 0.04 and 2.62 ± 0.34 days, respectively. The fully grown of the fifth instar will build cocoon up the apex of the fig leaf. The prepupa stage was 1 day. The pupa is developed within the pupal case for 4.00-5.75 days (average 4.85 ± 0.50 days for male pupa and 4.99 ± 0.50 for female pupa.