New Records of Insects Associated with Bornean Endemic Dipterocarp Seedlings
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Biosecurity Plan for the Vegetable Industry
Biosecurity Plan for the Vegetable Industry A shared responsibility between government and industry Version 3.0 May 2018 Plant Health AUSTRALIA Location: Level 1 1 Phipps Close DEAKIN ACT 2600 Phone: +61 2 6215 7700 Fax: +61 2 6260 4321 E-mail: [email protected] Visit our web site: www.planthealthaustralia.com.au An electronic copy of this plan is available through the email address listed above. © Plant Health Australia Limited 2018 Copyright in this publication is owned by Plant Health Australia Limited, except when content has been provided by other contributors, in which case copyright may be owned by another person. With the exception of any material protected by a trade mark, this publication is licensed under a Creative Commons Attribution-No Derivs 3.0 Australia licence. Any use of this publication, other than as authorised under this licence or copyright law, is prohibited. http://creativecommons.org/licenses/by-nd/3.0/ - This details the relevant licence conditions, including the full legal code. This licence allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to Plant Health Australia (as below). In referencing this document, the preferred citation is: Plant Health Australia Ltd (2018) Biosecurity Plan for the Vegetable Industry (Version 3.0 – 2018) Plant Health Australia, Canberra, ACT. This project has been funded by Hort Innovation, using the vegetable research and development levy and contributions from the Australian Government. Hort Innovation is the grower-owned, not for profit research and development corporation for Australian horticulture Disclaimer: The material contained in this publication is produced for general information only. -
Tropical Plant-Animal Interactions: Linking Defaunation with Seed Predation, and Resource- Dependent Co-Occurrence
University of Montana ScholarWorks at University of Montana Graduate Student Theses, Dissertations, & Professional Papers Graduate School 2021 TROPICAL PLANT-ANIMAL INTERACTIONS: LINKING DEFAUNATION WITH SEED PREDATION, AND RESOURCE- DEPENDENT CO-OCCURRENCE Peter Jeffrey Williams Follow this and additional works at: https://scholarworks.umt.edu/etd Let us know how access to this document benefits ou.y Recommended Citation Williams, Peter Jeffrey, "TROPICAL PLANT-ANIMAL INTERACTIONS: LINKING DEFAUNATION WITH SEED PREDATION, AND RESOURCE-DEPENDENT CO-OCCURRENCE" (2021). Graduate Student Theses, Dissertations, & Professional Papers. 11777. https://scholarworks.umt.edu/etd/11777 This Dissertation is brought to you for free and open access by the Graduate School at ScholarWorks at University of Montana. It has been accepted for inclusion in Graduate Student Theses, Dissertations, & Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. TROPICAL PLANT-ANIMAL INTERACTIONS: LINKING DEFAUNATION WITH SEED PREDATION, AND RESOURCE-DEPENDENT CO-OCCURRENCE By PETER JEFFREY WILLIAMS B.S., University of Minnesota, Minneapolis, MN, 2014 Dissertation presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biology – Ecology and Evolution The University of Montana Missoula, MT May 2021 Approved by: Scott Whittenburg, Graduate School Dean Jedediah F. Brodie, Chair Division of Biological Sciences Wildlife Biology Program John L. Maron Division of Biological Sciences Joshua J. Millspaugh Wildlife Biology Program Kim R. McConkey School of Environmental and Geographical Sciences University of Nottingham Malaysia Williams, Peter, Ph.D., Spring 2021 Biology Tropical plant-animal interactions: linking defaunation with seed predation, and resource- dependent co-occurrence Chairperson: Jedediah F. -
(Dipterocarpaceae) in the Philippines
Randy Alfabete Villarin (Autor) Genetic variation patterns of Shorea contorta and Parashorea malaanonan (Dipterocarpaceae) in the Philippines https://cuvillier.de/de/shop/publications/6361 Copyright: Cuvillier Verlag, Inhaberin Annette Jentzsch-Cuvillier, Nonnenstieg 8, 37075 Göttingen, Germany Telefon: +49 (0)551 54724-0, E-Mail: [email protected], Website: https://cuvillier.de 1 GENERAL INTRODUCTION The tropical rainforests in Southeast Asia are globally significant and considered to be among the most diverse forests in the world harboring a large proportion of the world’s biodiversity (Myers et al., 2000; Davies et al., 2005). The tree communities in this ecosystem are dominated by a species-rich family, the Dipterocarpaceae (Ashton, 1982; Proctor et al., 1983; Newman et al., 1996, 1998; Brearley et al., 2004; Slik et al., 2009). This family is one of the most well-known trees in the tropics (Appanah and Turnbull, 1998) and the species are considered to be most important both from the ecological and economic points of view (Lamprecht, 1989). Dipterocarps occur in the lowland forest with up to 80% of the emergent individuals and 40% understorey trees (Ashton, 1982). In the Philippines, they are mostly found in groups with other species occurring in relatively dense stands (Lomibao, 1973). During the past century, however, the Philippine forests were vastly denuded due to logging, fuel wood gathering and charcoal making, shifting cultivation and permanent agriculture (Kummer, 1992; FMB-DENR, 1999). There was a rapid loss of the forests from 21M hectare in 1900 to less than 6M hectares in 1996 (DENR, 2002), a scenario considered to be one of the most severe forest destructions in the world (Heaney, 1998). -
THE DISTRIBUTION of the DIPTEROCARPACEAE in THAILAND by Tern Sm Itinand (Read at Xitb Pacific Science Congress, Tokyo, 1St September 1966)
THE DISTRIBUTION OF THE DIPTEROCARPACEAE IN THAILAND by Tern Sm itinand (Read at XItb Pacific Science Congress, Tokyo, 1st September 1966) ABSTRACT The family Dipterocarpaceae is represented in Thailand by 9 genera and 6 3 species, and can be classified into 2 groups, evergreen and deciduous or xerophytic. The majority belong to the evergreen, which is scattered all over the country either in gallery forest (Dij;tero carpus alatus, VaLica cinerea and Hopea odorata), along the hill streams (Dipterocarpus oblongifolius and V atica odorata), in the low-lying land (Dij;terocarpus baudii, D. dyeri, D. gmcilis, D. clwrtaceus, D. ken·ii, Slwrea and f-loj;ea spp.), or on bill slopes (Dij;terocarpus cnslatus, D. gt·andiflorus, D. Tetusus, D. turbinatus, D . IIWC1"0carpus, Hopea odomta, I-Iopea f enea and S!wrea talura). Only 5 xerophytic species are represented (Dipterocmpus obtusifolius, D. tuberculatus, D. intn·catus, Shorea obtusa and Pe11taC11·1e suavi.s), occupying either the high plateau or ridges, and forming a climatic forest type, the Dry Deciduous Diptero carp forest. The highest elevation reached by the Dipterocarps is 1300 m.a.s.l. (D1j;terocarpus tuberculatus, D. obtusifolius, Shot·ea obtusa and Pentacme suavis). Parashortea stellata and Shorea Togersiana follow the Tenesserim tract, while Cotylelobium lanceolatum, Balanocarpus heimii, Shorea curtisii, S. assamica var. globifera, S. guiso, S. faguetiana, S. hemsleyana, S. sumatrana, S. mae1·optera, S. glauca S. j;arv lfolia, I-Iopea pedicellata, I-I. lat1jolia, Vatica staj;fiana, and V. lowii are confined to the Peninsular region not beyond the latitude 1 o·N. Species found only in the Northeastern region are I-Iopea 1·eticulata and I-I. -
Karyomorphology and Its Evolution in Dipterocarpaceae (Malvales)
© 2020 The Japan Mendel Society Cytologia 85(2): 141–149 Karyomorphology and Its Evolution in Dipterocarpaceae (Malvales) Kazuo Oginuma1*, Shawn Y. K. Lum2 and Hiroshi Tobe3 1 The Community Center for the Advancement of Education and Research at the University of Kochi, 5–15 Eikokuji-cho, Kochi 780–8515, Japan 2 Asian School of the Environment, Nanyang Technological University, Singapore 639798 3 Department of Botany, Graduate School of Science, Kyoto University, Kyoto 606–8502, Japan Received January 16, 2020; accepted February 9, 2020 Summary Previous chromosome information is restricted to Dipterocarpoideae, one of the two subfamilies of Dipterocarpaceae, and no chromosome information is available for another subfamily Monotoideae. Here we present the first karyomorphology of Marquesia macroura (2n=22) (Monotoideae), as well as of four species (2n=22) of four genera in tribe Dipterocarpeae and five species (2n=14) of tribe Shoreae in Dipterocarpoideae. Comparisons within Dipterocarpaceae and with Sarcolaenaceae (2n=22) sister to Dipetrocarpaceae in the light of phylogenetic relationships show that the basic chromosome number x=11 is plesiomorphic and x=7 apomor- phic in Dipterocapaceae. Based on available information, tribe Shoreae (x=7) has a uniform karyotype where all chromosomes have a centromere at median position, while the rest of the family (x=11) have a diverse karyotype in terms of the frequency of chromosomes with a centromere at median, submedian and subterminal position. We discussed the meaning of lability of karyotype in chromosome evolution. Keywords Basic chromosome number, Chromosome evolution, Dipterocarpaceae, Karyomorphology. Dipterocarpaceae (Malvales) are a family of 16 gen- x=10, and five genera Dryobalanops, Hopea, Neobala- era and 680 species distributed in tropical regions of nocarpus, Parashorea and Shorea of tribe Shoreae all the Old World, especially in the rain forests of Malesia have x=7. -
Aravalli Range of Rajasthan and Special Thanks to Sh
Occasional Paper No. 353 Studies on Odonata and Lepidoptera fauna of foothills of Aravalli Range, Rajasthan Gaurav Sharma ZOOLOGICAL SURVEY OF INDIA OCCASIONAL PAPER NO. 353 RECORDS OF THE ZOOLOGICAL SURVEY OF INDIA Studies on Odonata and Lepidoptera fauna of foothills of Aravalli Range, Rajasthan GAURAV SHARMA Zoological Survey of India, Desert Regional Centre, Jodhpur-342 005, Rajasthan Present Address : Zoological Survey of India, M-Block, New Alipore, Kolkata - 700 053 Edited by the Director, Zoological Survey of India, Kolkata Zoological Survey of India Kolkata CITATION Gaurav Sharma. 2014. Studies on Odonata and Lepidoptera fauna of foothills of Aravalli Range, Rajasthan. Rec. zool. Surv. India, Occ. Paper No., 353 : 1-104. (Published by the Director, Zool. Surv. India, Kolkata) Published : April, 2014 ISBN 978-81-8171-360-5 © Govt. of India, 2014 ALL RIGHTS RESERVED . No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without the prior permission of the publisher. This book is sold subject to the condition that it shall not, by way of trade, be lent, resold hired out or otherwise disposed of without the publisher’s consent, in any form of binding or cover other than that in which, it is published. The correct price of this publication is the price printed on this page. Any revised price indicated by a rubber stamp or by a sticker or by any other means is incorrect and should be unacceptable. PRICE Indian Rs. 800.00 Foreign : $ 40; £ 30 Published at the Publication Division by the Director Zoological Survey of India, M-Block, New Alipore, Kolkata - 700053 and printed at Calcutta Repro Graphics, Kolkata - 700 006. -
Interesting Early Stages of Some Sri Lankan Moths Typical Moth Life Cycle
Interesting early stages of some Sri Lankan Moths Typical Moth Life Cycle A Cocoon is a casing of spun silk produced by many insects to form a protective covering for the Pupa. Many Moth Caterpillars for example produce silk cocoons. Cocoons can be of various types, from hard to soft, with various colours dependent on the species involved. Wingless Females Some female moths of the Subfamily Lymantriinae are flightless. Male Female Orgyia sp. Lymantria sp. Life Cycle of Lymantria ampla Life cycle of Fir tussock moth (Orgyia detrita) Ant-mimic Moth caterpillars • Caterpillars in the moth genus, Homodes Guenée have been documented to be closely associated with weaver ants, as well as resembling them in terms of morphology and behaviour (Shelford, 1902, 1916; Kalshoven, 1961; Common, 1990; Holloway, 2005). In Sri Lanka, at least three species have been previously recorded • Homodes fulva • Homodes crocea Homodes crocea • Homodes vivida Dorsal (a) and posterior (b) views of the raised rear end of the caterpillar, Lobster Moth (Stauropus alternus) • First instar larva is a very good ant mimic both in appearance and behaviour • Resting posture of its mid instar look like an irregularly curved, dead leaf. • This resemblance to dried or dead leaf debris is certainly applicable to the later instars as well. Bagworms (Psychidae) • The bagworm family (Lepidoptera: Psychidae) includes approximately 1000 species, all of which complete larval development within a self enclosing bag. • In Sri Lanka 23 species have been recorded in this family • Some bagworms are specialized in their host plants (monophagous) , while others can feed on a variety of plant species (polyphagous) Eumeta variegata • A bagworm begins to build its case as soon as it hatches. -
The World's First Inquiline Flatid
TABLE OF CONTENTS KEYNOTE SPEAKERS Deep transcriptome insights into cave beetle eyes 1 Marcus Friedrich Aedes control: the future is now! 2 Hoffmann, A.A. The Hemipteroid Tree of Life 3 Kevin P. Johnson Biosecurity in northern Australia 4 James A. Walker Seeing at the limits: vision and visual navigation in nocturnal insects 5 Eric Warrant ORAL PRESENTATIONS Dung beetle (Coleoptera, Scarabaeidae) abundance and diversity at nature preserve within hyper-arid ecosystem of Arabian Peninsula 6 Abdel-Dayem, M., Kondratieff, B., Fadl , H.(1) and Aldhafer, H. Screening of sugarcane cultivars to assess the incidence against Chilo infuscatellus (Pyralidae, Lepidoptera) 6 Ahmad, S., Qurban, A. and Zahid, A. Microbiology and nutritional composition of some edible insects 7 Amadi, E.N. Studies on the mopane worm, Imbrasia belina an edible caterpillar 7 Allotey, J. DNA barcoding identification of mosquitoes using traditional and next-generation sequencing techniques 8 Batovska, J., Lynch, S., Cogan, N., Brown, K. and Blacket, M.J. Towards a compelling phylogeny of cyclorrhaphan flies (Diptera) using whole body adult transcriptomes 9 Bayless, K.M., Trautwein, M.D., Meusemann, K., Yeates, D.K. and Wiegmann, B.M. Establishing a population genetics toolbox and regional spatial database to facilitate identfying the incursion origin of the dengue mosquito Aedes aeqypti and the Asian tiger Ae. albopictus 10 Beebe, N.W. A summary of interceptions and additions to the New Zealand fauna, with reference to Australian origins 11 Bennett, S.J. The role of nutrition in determining individual and group patterns of behaviour 12 Berville, L., Hoffmann, B. and Suarez, A. Australian millipede diversity: an update 13 Black, D. -
Seasonally Dependent Relationship Between Insect Herbivores and Host Plant Density in Jatropha Nana, a Tropical Perennial Herb Ashish N
© 2018. Published by The Company of Biologists Ltd | Biology Open (2018) 7, bio035071. doi:10.1242/bio.035071 RESEARCH ARTICLE Seasonally dependent relationship between insect herbivores and host plant density in Jatropha nana, a tropical perennial herb Ashish N. Nerlekar ABSTRACT Out of the several hypotheses that seek to explain the relation The fact that plant spatial aggregation patterns shape insect- between host plant heterogeneity, spatial complexity and insect- ‘ herbivore communities in a variety of ways has resulted in a large herbivore characteristics, three key hypotheses are the enemies ’ ‘ ’ body of literature on the subject. The landmark resource hypothesis , the resource concentration hypothesis , and the ‘ ’ concentration hypothesis predicts that density of insect herbivores resource dilution hypothesis (Elton, 1958; Root, 1973; Otway ‘ ’ per plant will increase as host plant density increases. I examined this et al., 2005; Björkman et al., 2010). The enemies hypothesis prediction across temporal samplings using Jatropha nana and the predicts that because of higher predator and parasite efficiency associated specialist insect herbivores as a system. Through 12 field in diverse environments, insect herbivores are less abundant in samplings, I modelled the effect of host plant density on insect- species-diverse plant communities than in simple (e.g. monoculture) ‘ ’ herbivore loads. The initial samplings (2–3) provided evidence for the communities (Elton, 1958). The resource concentration hypothesis resource concentration hypothesis, with insect loads increasing with (RCH) goes further to consider host patch size and plant density as increasing host plant density, whereas the later samplings (4–5, predictors of herbivore abundance, along with plant diversity (Root, 7–11) showed the opposite; a resource dilution pattern with a decline 1973). -
Prevention and Control of Harmful Insects on Tropical and Subtropical Fruits in Vietnam
JIRCAS International Symposium Series No. 3: 67-73 Session 3-2 67 Prevention and Control of Harmful Insects on Tropical and Subtropical Fruits in Vietnam Nguyen Ngoc KIEM' Abstract Pests and diseases, in particular harmful insects have caused heavy losses to the produc tion of tropical and subtropical fruits. A large number of species of insects affecting tropical and subtropical fruits have been reported in the world. However, in different regions of the tropics and subtropics, the num ber of insect species and the extent of their destructive effects are different. This paper fo cused on the most serious insects affecting the major fruits occurring in Vietnam, a country in the Asia-Pacific Region with natural conditions conducive to the production of many tropical and subtropical fruits. Such insects include : banana core borer weevil ( Odoiporus longicollis Olivier), pineapple root-borer (Adore/us chinensis Thunber), pineapple aphid (Dis micoccus brevipes), citrus core borers, citrus. leaf weevil (Hypomeces squamosus Fabr. and Platymycterus sirversi), citrus. sucking moths (Chelidonium argentatum (Dalman), Nadezhdiella Cantoni (Hope) and Anaplophora chinensis Forester) (Othreis Ju/Ionia Clerck and others), Citras oriental fruit fly (Dacus dorsalis), citrus. leaf miner (Phyllocnistis citrella), Diaphorina citri, litchi stink bug (Tessaratoma papil/osa), litchi erinose mite (Eriophes litchi), etc. Research projects have been carried out to promote the production by applying different measures including chemical control, biological control, etc. Introduction Vietnam, a country in the Southeast Asia-Pacific region, with a monsoon-tropical climate and cold winter, produces many tropical and subtropical fruits, including 130 species belonging to 39 botanical families (Tran The Tue, 1982). -
Forestry Department Food and Agriculture Organization of the United Nations
Forestry Department Food and Agriculture Organization of the United Nations Forest Health & Biosecurity Working Papers OVERVIEW OF FOREST PESTS THAILAND January 2007 Forest Resources Development Service Working Paper FBS/32E Forest Management Division FAO, Rome, Italy Forestry Department Overview of forest pests – Thailand DISCLAIMER The aim of this document is to give an overview of the forest pest1 situation in Thailand. It is not intended to be a comprehensive review. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. © FAO 2007 1 Pest: Any species, strain or biotype of plant, animal or pathogenic agent injurious to plants or plant products (FAO, 2004). ii Overview of forest pests – Thailand TABLE OF CONTENTS Introduction..................................................................................................................... 1 Forest pests...................................................................................................................... 1 Naturally regenerating forests..................................................................................... 1 Insects ..................................................................................................................... 1 Diseases.................................................................................................................. -
Insect Pests and Insect-Vectored Diseases of Palmsaen 724 328..342
Australian Journal of Entomology (2009) 48, 328–342 Insect pests and insect-vectored diseases of palmsaen_724 328..342 Catherine W Gitau,1* Geoff M Gurr,1 Charles F Dewhurst,2 Murray J Fletcher3 and Andrew Mitchell4 1EH Graham Centre for Agricultural Innovation, Charles Sturt University, PO Box 883 Orange, NSW 2800, Australia. 2PNG Oil Palm Research Association, Kimbe, West New Britain, Papua New Guinea. 3NSW Department of Primary Industries, Orange Agricultural Institute, Orange, NSW 2800, Australia. 4NSW Department of Primary Industries, Wagga Wagga Agricultural Institute, Wagga Wagga, NSW 2650, Australia. Abstract Palm production faces serious challenges ranging from diseases to damage by insect pests, all of which may reduce productivity by as much as 30%. A number of disorders of unknown aetiology but associated with insects are now recognised. Management practices that ensure the sustainability of palm production systems require a sound understanding of the interactions between biological systems and palms. This paper discusses insect pests that attack palms, pathogens the insects vector as well as other disorders that are associated with these pests. We re-examine the disease aetiologies and procedures that have been used to understand causality. Pest management approaches such as cultural and biological control are discussed. Key words aetiology, Arecaceae, diagnosis, pathosystems, pest management. INTRODUCTION has transported them from their native habitats to new loca- tions. For example, the date palm is believed to have originated In many cultures, palms are a symbol of splendour, peace, in the Persian Gulf and North Africa but it is now grown victory and fertility. Palms constitute one of the best-known worldwide in semi-arid regions (Zaid 1999).