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Amphiesmeno- Ptera: the Caddisflies and Lepidoptera
CY501-C13[548-606].qxd 2/16/05 12:17 AM Page 548 quark11 27B:CY501:Chapters:Chapter-13: 13Amphiesmeno-Amphiesmenoptera: The ptera:Caddisflies The and Lepidoptera With very few exceptions the life histories of the orders Tri- from Old English traveling cadice men, who pinned bits of choptera (caddisflies)Caddisflies and Lepidoptera (moths and butter- cloth to their and coats to advertise their fabrics. A few species flies) are extremely different; the former have aquatic larvae, actually have terrestrial larvae, but even these are relegated to and the latter nearly always have terrestrial, plant-feeding wet leaf litter, so many defining features of the order concern caterpillars. Nonetheless, the close relationship of these two larval adaptations for an almost wholly aquatic lifestyle (Wig- orders hasLepidoptera essentially never been disputed and is supported gins, 1977, 1996). For example, larvae are apneustic (without by strong morphological (Kristensen, 1975, 1991), molecular spiracles) and respire through a thin, permeable cuticle, (Wheeler et al., 2001; Whiting, 2002), and paleontological evi- some of which have filamentous abdominal gills that are sim- dence. Synapomorphies linking these two orders include het- ple or intricately branched (Figure 13.3). Antennae and the erogametic females; a pair of glands on sternite V (found in tentorium of larvae are reduced, though functional signifi- Trichoptera and in basal moths); dense, long setae on the cance of these features is unknown. Larvae do not have pro- wing membrane (which are modified into scales in Lepi- legs on most abdominal segments, save for a pair of anal pro- doptera); forewing with the anal veins looping up to form a legs that have sclerotized hooks for anchoring the larva in its double “Y” configuration; larva with a fused hypopharynx case. -
Papilionidae)
180 JOURNAL OF THE LEPIDOPTERISTS' SOCIETY NOTES ON THE BIOLOGIES OF PAPILlO LAGLAIZEI AND P. TOBOROI (PAPILIONIDAE) R. STRAATMAN Sogeri, Papua, New Guinea Papilio laglaizei Depuiset and P. toboroi Ribbe are included in a small and closely related species group that is morphologically distinctive from other species in the genus (Munroe, 1958). P. laglaizei is found on mainland New Guinea, and P. tohoroi occurs on Bougainville, Santa Ysabel and Malaita Island. A third species, P. moerneri Aurivillius, is known from New Ireland. What some recognise as P. mayrhoferi Bang-Haas from New Britain probably is only a geographical race of P. moerneri as was originally described by Bang-Haas (1939). In addition to the two specimens of typical P. moerneri mentioned by D'Abrera (1971), there is one in the Australian National Insect Collec tion, Canberra, and the author has also seen a few specimens taken on New Ireland in 1968. In view of the foregoing, and the fact that at least some known localities of the species on New Ireland have hardly been disturbed during this century, D'Abrera's (op. cit.) suggestion that the species is "probably extinct" is considered unlikely to be correct. The adult of P. laglaizei shows a remarkable similarity to the common and presumably distasteful diurnal moth Alcides agathyrsus Kirsch (Uraniidae). The two species also share some of the same habitats. These factors suggest a possible mimicry situation. Papilio tohoroi and P. moerneri, although co-existing in the same habitats with other diurnal Alcides species, do not particularly resemble them. The biology of this Papilio species group is remarkable in other aspects, e.g., the laying of eggs in large masses and the highly gregarious behaviour of the larvae (D'Abrera, 1971). -
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.................................................................................................................. -
Evolution of the Insects David Grimaldi and Michael S
Cambridge University Press 0521821495 - Evolution of the Insects David Grimaldi and Michael S. Engel Index More information INDEX 12S rDNA, 32, 228, 269 Aenetus, 557 91; general, 57; inclusions, 57; menageries 16S rDNA, 32, 60, 237, 249, 269 Aenigmatiinae, 536 in, 56; Mexican, 55; parasitism in, 57; 18S rDNA, 32, 60, 61, 158, 228, 274, 275, 285, Aenne, 489 preservation in, 58; resinite, 55; sub-fossil 304, 307, 335, 360, 366, 369, 395, 399, 402, Aeolothripidae, 284, 285, 286 resin, 57; symbioses in, 303; taphonomy, 468, 475 Aeshnoidea, 187 57 28S rDNA, 32, 158, 278, 402, 468, 475, 522, 526 African rock crawlers (see Ambermantis wozniaki, 259 Mantophasmatodea) Amblycera, 274, 278 A Afroclinocera, 630 Amblyoponini, 446, 490 aardvark, 638 Agaonidae, 573, 616: fossil, 423 Amblypygida, 99, 104, 105: in amber, 104 abdomen: function, 131; structure, 131–136 Agaoninae, 423 Amborella trichopoda, 613, 620 Abies, 410 Agassiz, Alexander, 26 Ameghinoia, 450, 632 Abrocomophagidae, 274 Agathiphaga, 560 Ameletopsidae, 628 Acacia, 283 Agathiphagidae, 561, 562, 567, 630 American Museum of Natural History, 26, 87, acalyptrate Diptera: ecological diversity, 540; Agathis, 76 91 taxonomy, 540 Agelaia, 439 Amesiginae, 630 Acanthocnemidae, 391 ages, using fossils, 37–39; using DNA, 38–40 ametaboly, 331 Acari, 99, 105–107: diversity, 101, fossils, 53, Ageniellini, 435 amino acids: racemization, 61 105–107; in-Cretaceous amber, 105, 106 Aglaspidida, 99 ammonites, 63, 642 Aceraceae, 413 Aglia, 582 Amorphoscelidae, 254, 257 Acerentomoidea, 113 Agrias, 600 Amphientomidae, -
Optical Modelling and Phylogenetic Analysis Provide Clues to the Likely Function of Corneal Nipple Arrays in Butterflies and Moths
insects Article Optical Modelling and Phylogenetic Analysis Provide Clues to the Likely Function of Corneal Nipple Arrays in Butterflies and Moths Adrian Spalding 1,2,* , Katie Shanks 3 , Jon Bennie 4, Ursula Potter 5 and Richard ffrench-Constant 1 1 Centre for Ecology and Conservation, University of Exeter in Cornwall, Penryn Campus, Penryn TR10 9FE, UK 2 Spalding Associates (Environmental) Ltd., 10 Walsingham Place, Truro TR1 2RP, UK 3 Environment and Sustainability Institute, University of Exeter Penryn Campus, Penryn TR10 9FE, UK 4 Centre for Geography and Environmental Science, Peter Lanyon Building, Penryn Campus, Treliever Road, Penryn, Cornwall, PenrynTR10 9FE, UK 5 Microscopy & Analysis Suite, Faculty of Science, University of Bath, Claverton Down, Bath BA2 7AY, UK * Correspondence: [email protected]; Tel.: +44-(0)1-872-272-711 Received: 22 July 2019; Accepted: 19 August 2019; Published: 22 August 2019 Abstract: The lenses in compound eyes of butterflies and moths contain an array of nipple-shaped protuberances, or corneal nipples. Previous work has suggested that these nipples increase light transmittance and reduce the eye glare of moths that are inactive during the day. This work builds on but goes further than earlier analyses suggesting a functional role for these structures including, for the first time, an explanation of why moths are attracted to UV light. Using a phylogenetic approach and 3D optical modelling, we show empirically that these arrays have been independently lost from different groups of moths and butterflies and vary within families. We find differences in the shape of nipples between nocturnal and diurnal species, and that anti-glow reflectance levels are different at different wave-lengths, a result thereby contradicting the currently accepted theory of eye glow for predator avoidance. -
Zootaxa, Annotated Checklist of Weevils from the Papuan Region
ZOOTAXA 1536 Annotated checklist of weevils from the Papuan region (Coleoptera, Curculionoidea) GREGORY P. SETLIFF Magnolia Press Auckland, New Zealand Zootaxa 1536 © 2007 Magnolia Press · 1 Gregory P. Setliff Annotated checklist of weevils from the Papuan region (Coleoptera, Curculionoidea) (Zootaxa 1536) 296 pp.; 30 cm. 30 July 2007 ISBN 978-1-86977-139-3 (paperback) ISBN 978-1-86977-140-9 (Online edition) FIRST PUBLISHED IN 2007 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2007 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. This authorization does not extend to any other kind of copying, by any means, in any form, and for any purpose other than private research use. ISSN 1175-5326 (Print edition) ISSN 1175-5334 (Online edition) 2 · Zootaxa 1536 © 2007 Magnolia Press SETLIFF Zootaxa 1536: 1–296 (2007) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2007 · Magnolia Press ISSN 1175-5334 (online edition) Annotated checklist of weevils from the Papuan region (Coleoptera, Curculionoidea) GREGORY P. SETLIFF Department of Entomology, University of Minnesota, 219 Hodson, 1980 Folwell Avenue, St. Paul, Minnesota 55108 U.S.A. & The New Guinea Binatang Research Center, P. O. Box 604, Madang, Papua New Guinea. -
Estimating Time and Space in the Evolution of the Lepidoptera
Estimating time and space in the evolution of the Lepidoptera Rienk de Jong Several aspects of estimating what happened when and where in the evolution of the Lepidoptera are discussed. Because of their scarcity and often poor preservation, fossils are not very helpful, but at least they demonstrate that, in the Oligocene some taxa of butterflies, perhaps at tribal level or higher, did occur in the Northern as well as in the Southern Hemisphere. The concept of a molecular clock is seen as a most needed test for vicariance explanations of disjunct distributions. Special emphasis is laid on the importance of calibration of the clock. The use of geological vicariance events as calibration points is rejected, because of circularity when vicariance explanations are to be tested. Fossils as calibration points should ideally be replaced by the minimum age of an apomorphous character state demonstrated by the fossil rather than a supposed identity on the basis of overall similarity. Some conditions that directed the evolution of Lepidoptera (called constraints here) are discussed for their possible use as calibration points. Estimation of the evolution in space through time (palaeobiogeography) as found in recent literature is discussed, the often supposed role (of the break-up) of Gondwana in the evolution of the butterflies is challenged, and an alternative hypothesis is given. R. de Jong, National Museum of Natural History, P.O. Box 9517, 2300 RA Leiden, The Netherlands. E-mail: [email protected] Introduction extrapolate the data to far back in history and to Estimating time and space of events in the evolu- make use of (reputed) circumstantial evidence. -
Uraniidae) and Their System a Tic, Evolutionary, and Ecological Significance
Journal of the Lepidopterists' SOciety 45(4), 1991, 296-347 FOOD PLANT ASSOCIATIONS OF THE URANIINAE (URANIIDAE) AND THEIR SYSTEM A TIC, EVOLUTIONARY, AND ECOLOGICAL SIGNIFICANCE DAVID C, LEES Flat 6, 23 Normanton Road, South Croydon, Surrey, CR2 7 AE, United Kingdom AND NEAL G. SMITH Smithsonian Tropical Research Institute, Unit 0948, APO AA34002-0948 U.S.A. ABSTRACT. Larval and adult food plant records for the moth subfamily Uraniinae (sensu Sick 1937) are reviewed. Reliable larval food plant records for all seven genera include only the genera Omphalea L., Endospermum Benth., and Suregada Roxb. ex Rottl. (Euphorbiaceae), and this specialization on Euphorbiaceae supports Sick's concept of Uraniinae (based on meta thoracic and tympanal morphology) as a monophyletic group. Whereas Omphalea is known to be fed on only by larvae of the three strictly day-flying genera (Urania Fabricius, Chrysiridia Hiibner, and Alcides Hiibner), Endospermum is a recorded foodplant for Alcides and three primarily nocturnal genera (Lyssa Hiibner, Urapteroides Moore, and Cyphura Warren). The latter two genera have been traditionally included in the Microniinae, as has been Urapteritra Viette, whose larval food plant Suregada is reported here for the first time. Some ecological and evolutionary aspects of uraniine larval foodplant specialization are discussed. A putative phylogeny of Uraniinae based on published hearing organ and larval morphology is presented, and the phylo genetic significance of larval foodplant relationships evaluated. Adult foodplants (nectar resources) for the diurnal uraniines are summarized, and the possibility of their role in the moths' reproductive or predator defense ecology is briefly discussed. Additional key words: Microniinae, Omphalea, Endospermum, Suregada, Euphor biaceae. -
References 255
References 255 References Banks, A. et al. (19902): Pesticide Application Manual; Queensland Department of Primary Industries; Bris- bane; Australia Abercrombie, M. et al. (19928): Dictionary of Biology; Penguin Books; London; UK Barberis, G. and Chiaradia-Bousquet, J.-P. (1995): Pesti- Abrahamsen, W.G. (1989): Plant-Animal Interactions; cide Registration Legislation; Food and Agriculture McGraw-Hill; New York; USA Organisation (FAO) Legislative Study No. 51; Rome; D’Abrera, B. (1986): Sphingidae Mundi: Hawk Moths of Italy the World; E.W. Classey; London; UK Barbosa, P. and Schulz, J.C., (eds.) (1987): Insect D’Abrera, B. (19903): Butterflies of the Australian Outbreaks; Academic Press; San Diego; USA Region; Landsowne Press; Melbourne; Australia Barbosa, P. and Wagner, M.R. (1989): Introduction to Ackery, P.R. (ed.) (1988): The Biology of Butterflies; Forest and Shade Tree Insects; Academic Press; San Princeton University press; Princeton; USA Diego; USA Adey, M., Walker P. and Walker P.T. (1986): Pest Barlow, H.S. (1982): An Introduction to the Moths of Control safe for Bees: A Manual and Directory for the South East Asia; Malaysian Nature Society; Kuala Tropics and Subtropics; International Bee Research Lumpur; Malaysia; Distributor: E.W. Classey; Association; Bucks; UK Farrington; P.O. Box 93; Oxon; SN 77 DR 46; UK Agricultural Requisites Scheme for Asia and the Pacific, Barrass, R. (1974): The Locust: A Guide for Laboratory South Pacific Commission (ARSAP/CIRAD/SPC) Practical Work; Heinemann Educational Books; (1994): Regional Agro-Pesticide Index; Vol. 1 & 2; London; UK Bangkok; Thailand Barrett, C. and Burns, A.N. (1951): Butterflies of Alcorn, J.B. (ed.) (1993): Papua New Guinea Conser- Australia and New Guinea; Seward; Melbourne; vation Needs Assessment; Vol. -
EUPHORBIACEAE) in RESPONSE to DAMAGE by Urania Fulgens WALK ER
ANATOMY, HISTOCHEMISTRY AND PHENOLIC COMPOUNDS CONTENT OF LEAVES FROM Omphalea oleifera Hemsl. (EUPHORBIACEAE) IN RESPONSE TO DAMAGE BY Urania fulgens WALK ER Silvia Espinosa-Matías, Roberto Enrique Llanos-Romero, Álvaro Delfino Campos Villanueva, Blanca Pérez-García, Josefina Herrera-Santoyo and Patricia Guevara-Fefer SUMMARY Leaves of Omphalea oleifera Hemsl. damaged by Urania crystals. The estimated amounts of lignin and cafeic, ferulic fulgens Walker were examined. Leaves were anatomically de- and chlorogenic acids were respectively 11% and 109.65, 16.58 scribed, histochemical tests were performed and the content of and 0.082µg·g-1 dry wt in the damaged leaves, whereas for the lignin and phenolic acids estimated. Morpho-anatomical fea- intact were 7%, 97.65, 5.48 and 0.051µg·g-1 dry wt. The results tures were similar in damaged leaves and the control, but mi- suggest that the insect damage triggers induced responses in nor histochemical differences were observed. The tissues adja- O. oleifera including production and accumulation of phenolic cent to the damage showed lignin deposits and calcium oxalate compounds and calcium oxalate crystals on the leaf tissues. Introducción niidae) primarily feed on stems, mushroom-shaped an- Plants exhibit a wide gamut Omphalea leaves (Lees and droecia, and large fruits (Ru- of induced responses to the Omphalea L. (Euphorbia- Smith, 1991). At the Estación dall, 1994a, b; Gillespie, 1997; damage caused by pathogens ceae) is a genus of canopy li- de Biología Tropical Los Gillespie and Ambruster, and herbivores. Particularly, anas, shrubs and trees, com- Tuxtlas, Veracruz, the larvae 1997). Regarding O. oleifera, the induced responses that prised of ~20 tropical species of Urania fulgens Walker the seedlings content of some currently decrease the nega- with centers of diversity and 1854 feed on O. -
Fig. 5-46: Diptera (Flies): (A) Leptotarsus Imperatorius (Tipulidae), (B) Simulium Sp
5. Evolution and Classification 131 A B C D E F G H I J K L M N O P Q Fig. 5-46: Diptera (Flies): (A) Leptotarsus imperatorius (Tipulidae), (B) Simulium sp. X (Simuliidae), (C) Atrichobrunnettia sp. C (Psychodidae), (D) Orfelia sp. X (Mycetophilidae), (E) Trichophthalma spp. (Tabanoidea), (F) Leptogaster sp. C (Asilidae), (G) Comptosia lateralis C (Bombyliidae), (H) Heteropsilopus sp. X (Dolichopodidae), (I) Eristalis sp. (Syrphidae), (J) X stalk-eyed fly Achias sp. (Platystomatidae), (K) Achias sp. C (Platystomatidae), (L) X antlered fly, (M†) larvae of Creatitis capitata (Tephritidae), (N†) pupa of Creatitis capitata (Tephritidae), (O†) adult fruit fly Creatitis capitata (Tephritidae), (P) Musca sp. X (Muscidae), (Q) Sarcorohdendorfia sp. C (Sarcophagidae) (reproduced from CSIRO, 1991; Hill, D.S. and Waller, J.M., 1988†; photos Schneider, M.F.) 132 5. Evolution and Classification wild as well as domesticated mammals, living The femora sometimes have a row of setae or amongst the feathers or hair of their host. The stout bristles on the outer surface. The adults flies are of economic importance since they have two pairs of functional, subequal infest livestock like sheep, horses and cattle. membranous wings that are folded roof-like A number of these pests are introduced. or flat above the body during rest. The wings show poor cross-venation. A wing coupling mechanism (frenulum) is present. Body and wings are densely covered with hairs and occasionally with groups of scales (fig. 5-47 B). The aquatic larvae have well developed chewing mouthparts, peg-like antennae, compound eyes, functional thoracic legs, one pair of abdominal prolegs and abdominal tracheal gills (fig. -
An Extinct Species in the Collection of the Upper Silesian Museum (Muzeum Górnolskie), Bytom, Poland (Lepidotpera: Uraniidae) SHILAP Revista De Lepidopterología, Vol
SHILAP Revista de Lepidopterología ISSN: 0300-5267 [email protected] Sociedad Hispano-Luso-Americana de Lepidopterología España Domagala, P.; Larysz, A.; Dobosz, R.; González, J. M. Urania sloanus (Cramer, 1779), an extinct species in the collection of the Upper Silesian Museum (Muzeum Górnolskie), Bytom, Poland (Lepidotpera: Uraniidae) SHILAP Revista de Lepidopterología, vol. 43, núm. 171, septiembre, 2015, pp. 455-460 Sociedad Hispano-Luso-Americana de Lepidopterología Madrid, España Available in: http://www.redalyc.org/articulo.oa?id=45543215012 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative 455-460 Urania sloanus (Crame 9/9/15 17:51 Página 455 SHILAP Revta. lepid., 43 (171), septiembre 2015: 455-460 eISSN: 2340-4078 ISSN: 0300-5267 Urania sloanus (Cramer, 1779), an extinct species in the collection of the Upper Silesian Museum (Muzeum Górnos´la˛skie), Bytom, Poland (Lepidoptera: Uraniidae) P. Domagala, A. Larysz, R. Dobosz & J. M. González Abstract Urania sloanus (Cramer, 1779) is an endemic Lepidoptera species from Jamaica. It is believed to be extinct since the end of the 19th century or the beginning of the 20th. While revising the exotic Lepidoptera’ collection of the Upper Silesian Museum in Bytom, Poland, a well preserved specimen of this species was found. As far as we know, it could be one of the very few specimens of that species in Polish museum collections. KEY WORDS: Lepidoptera, Uraniidae, Biodiversity, extinct species, Omphalea, Jamaica, Venezuela.