A Software System for Automated Identification and Retrieval of Moth
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Publications by David Lack
Publications by David Lack Books 1934 The Birds of Cambridgeshire. Cambridge Bird Club, Cambridge. 1943 The Life of the Robin. Witherby, London. 4th edn. (revised) 1965. 1947 Darwin's Finches. Cambridge University Press, Cambridge. Harper Torch book paperback edn. 1961. Japanese edn. 1974. 1950 Robin Redbreast. Oxford University Press, Oxford. 1954 The Natural Regulation of Animal Numbers. Clarendon Press, Oxford. Paperback edn. 1970. Russian edn. 1957. 1956 Swifts in a Tower. Methuen, London. 1957 Evolutionary Theory and Christian Belief. Methuen, London. Reprinted with new chapter 1961. 1965 Enjoying Ornithology. Methuen, London. 1966 Population Studies of Birds. Clarendon Press, Oxford. 1968 Ecological Adaptations for Breeding in Birds. Methuen, London. 1971 Ecological Isolation in Birds. Blackwell Scientific Publications, Oxford and Edinburgh. 1974 Evolution Illustrated by Waterfowl. Blackwell Scientific Publications, Oxford and Edinburgh. 1976 Island Biology. fllustrated by the Land birds of Jamaica. Blackwell Scientific Publications, Oxford and Edinburgh. Papers 1930 Double -brooding of the Nightjar. Br. Birds, 23, 242 - 244. 1930 Some diurnal observations on the Night jar. Land. Nat., 1930, pp. 47-55. 1930 Spring migration, 1930, at the Cambridge Sewage Farm. Br. Birds, 24, 145 -154. 1931 Coleoptera on St. Kilda in 1931.Entomologists' Monthly Mag., 47, 1 -4. 1931 Observations at sewage farms and reservoirs, 1930: Migration at Cambridge, autumn, 1930.Br. Birds, 24,280-282. 1932 Some breeding habits of the European Nightjar. Ibis, (13) 2, 266-284. 1932 Birds of Bear Island. Bull. Br. Omith. Qub, 53,64-69. 1932 With John Buchan and T. H. Harrisson. The early autumn migration at St. Kildain 193l.Scott.Nat., 1932,pp.1-8. -
Perspective Where Might Be Many Tropical Insects?
Biological Conservation 233 (2019) 102–108 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Perspective Perspective: Where might be many tropical insects? T ⁎ Daniel H. Janzen , Winnie Hallwachs Department of Biology, University of Pennsylvania, Philadelphia 19104, United States of America ABSTRACT I have been watching the gradual and very visible decline of Mexican and Central American insect density and species richness since 1953 and Winnie since 1978. The loss is very real for essentially all higher taxa, and the reasons are very evident: intense forest and agricultural simplification of very large areas, massive use of pesticides, habitat fragmentation, and at least since the 1980's, ever-increasing climate change in temperature, rainfall, and synchronization of seasonal cues. There is no ecological concept suggesting that this biodiversity and habitat impoverishment is restricted to this portion of the Neotropics, and our 50 years of occasional visits to other parts of the tropics suggest the same. We are losing most of the insect community that is still in the cloud forests due to the drying of the tops of tropical mountains, just as we are losing the huge expanses of insect communities that once occupied the fertile soils, weather, and water of the lowland tropics. Today we have unimaginable access to the world's biodiversity through the internet, roads, dwellings, education, bioliterate societies, DNA barcoding, genome sequencing, and human curiosity. The wild world gains from our understanding that it needs large and diverse terrain, relief from hunting trees and animals, site-specific restoration, profit-sharing with its societies, and tolerance of humans and our extended genomes. -
Recolecta De Artrópodos Para Prospección De La Biodiversidad En El Área De Conservación Guanacaste, Costa Rica
Rev. Biol. Trop. 52(1): 119-132, 2004 www.ucr.ac.cr www.ots.ac.cr www.ots.duke.edu Recolecta de artrópodos para prospección de la biodiversidad en el Área de Conservación Guanacaste, Costa Rica Vanessa Nielsen 1,2, Priscilla Hurtado1, Daniel H. Janzen3, Giselle Tamayo1 & Ana Sittenfeld1,4 1 Instituto Nacional de Biodiversidad (INBio), Santo Domingo de Heredia, Costa Rica. 2 Dirección actual: Escuela de Biología, Universidad de Costa Rica, 2060 San José, Costa Rica. 3 Department of Biology, University of Pennsylvania, Philadelphia, USA. 4 Dirección actual: Centro de Investigación en Biología Celular y Molecular, Universidad de Costa Rica. [email protected], [email protected], [email protected], [email protected], [email protected] Recibido 21-I-2003. Corregido 19-I-2004. Aceptado 04-II-2004. Abstract: This study describes the results and collection practices for obtaining arthropod samples to be stud- ied as potential sources of new medicines in a bioprospecting effort. From 1994 to 1998, 1800 arthropod sam- ples of 6-10 g were collected in 21 sites of the Área de Conservación Guancaste (A.C.G) in Northwestern Costa Rica. The samples corresponded to 642 species distributed in 21 orders and 95 families. Most of the collections were obtained in the rainy season and in the tropical rainforest and dry forest of the ACG. Samples were obtained from a diversity of arthropod orders: 49.72% of the samples collected corresponded to Lepidoptera, 15.75% to Coleoptera, 13.33% to Hymenoptera, 11.43% to Orthoptera, 6.75% to Hemiptera, 3.20% to Homoptera and 7.89% to other groups. -
The Insect Database in Dokdo, Korea: an Updated Version Includes 22 Newly Recorded Species on the Island and One Species in Korea
PREPRINT Posted on 14/12/2020 DOI: https://doi.org/10.3897/arphapreprints.e62027 The Insect database in Dokdo, Korea: An updated version includes 22 newly recorded species on the island and one species in Korea Jihun Ryu, Young-Kun Kim, Sang Jae Suh, Kwang Shik Choi Not peer-reviewed, not copy-edited manuscript. Not peer-reviewed, not copy-edited manuscript posted on December 14, 2020. DOI: https://doi.org/10.3897/arphapreprints.e62027 The Insect database in Dokdo, Korea: An updated version includes 22 newly recorded species on the island and one species in Korea Jihun Ryu‡,§, Young-Kun Kim |, Sang Jae Suh|, Kwang Shik Choi‡,§,¶ ‡ School of Life Science, BK21 Plus KNU Creative BioResearch Group, Kyungpook National University, Daegu, South Korea § Research Institute for Dok-do and Ulleung-do Island, Kyungpook National University, Daegu, South Korea | School of Applied Biosciences, Kyungpook National University, Daegu, South Korea ¶ Research Institute for Phylogenomics and Evolution, Kyungpook National University, Daegu, South Korea Corresponding author: Kwang Shik Choi ([email protected]) Abstract Background Dokdo, an island toward the East Coast of South Korea, comprises 89 small islands. Dokdo is a volcanic island created by a volcanic eruption that promoted the formation of Ulleungdo (located in the East sea), which is ~87.525 km away from Dokdo. Dokdo is an important island because of geopolitics; however, because of certain investigation barriers such as weather and time constraints, the awareness of its insect fauna is less compared to that of Ulleungdo. Dokdo’s insect fauna was obtained as 10 orders, 74 families, and 165 species until 2017; subsequently, from 2018 to 2019, 23 unrecorded species were discovered via an insect survey. -
Diurnal and Nocturnal Lepidoptera of Buenaventura (Piñas-Ecuador) Lepidópteros Diurnos Y Nocturnos De La Reserva Buenaventura (Piñas –Ecuador)
Volume 9 (1) Diurnal and nocturnal lepidoptera of Buenaventura (Piñas-Ecuador) Lepidópteros diurnos y nocturnos de la Reserva Buenaventura (Piñas –Ecuador) Sebastián Padrón Universidad del Azuay Escuela de Biología del Medio Ambiente [email protected] February 2006 Download at: http://www.lyonia.org/downloadPDF.php?pdfID=2.408.1 Diurnal and nocturnal lepidoptera of Buenaventura (Piñas-Ecuador) Resumen En un bosque húmedo tropical en el sur de Ecuador, dentro de un gradiente altitudinal de 600-1000m sobre el nivel del mar, se realizo un inventario de mariposas diurnas y nocturnas elaborando así una lista preliminar de especies. La región de investigación (La Reserva Buenaventura) está ubicada en la parte alta de la provincia del Oro cerca de la ciudad de Piñas, esta reserva presenta una gran diversidad de aves, especies vegetales e insectos. Las comunidades de mariposas diurnas y nocturnas fueron muestreadas durante los meses de Agosto y Septiembre del 2004, para lo cual se utilizo trampas aéreas, de cebo, e intercepción con red y de luz Vapor de Mercurio 250 watt. Las trampas aéreas, de cebo y de intercepción fueron efectuadas a lo largo de transectos definidos dentro de la reserva, estos fueron monitoreados cada dos días dentro de los 24 días de la investigación. La trampa de luz fue ubicada en la estación científica y esta se uso, por tres horas desde 18:30 hasta 21:30, durante 15 noches. Se pudo capturar 550 especimenes las cuales fueron conservadas, montadas e identificación. Se pudo clasificar 255 especies de lepidópteros de las cuales 60 pertenecen a mariposas diurnas y 195 a nocturnas. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
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. -
Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis
ANRV330-EN53-23 ARI 2 November 2007 18:40 Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis James B. Whitfield1 and Karl M. Kjer2 1Department of Entomology, University of Illinois, Urbana, Illinois 61821; email: jwhitfi[email protected] 2Department of Ecology, Evolution and Natural Resources, Rutgers University, New Brunswick, New Jersey 08901; email: [email protected] Annu. Rev. Entomol. 2008. 53:449–72 Key Words First published online as a Review in Advance on diversification, molecular evolution, Palaeoptera, Orthopteroidea, September 17, 2007 fossils The Annual Review of Entomology is online at ento.annualreviews.org Abstract by UNIVERSITY OF ILLINOIS on 12/18/07. For personal use only. This article’s doi: Phylogenies of major groups of insects based on both morphological 10.1146/annurev.ento.53.103106.093304 and molecular data have sometimes been contentious, often lacking Copyright c 2008 by Annual Reviews. the data to distinguish between alternative views of relationships. Annu. Rev. Entomol. 2008.53:449-472. Downloaded from arjournals.annualreviews.org All rights reserved This paucity of data is often due to real biological and historical 0066-4170/08/0107-0449$20.00 causes, such as shortness of time spans between divergences for evo- lution to occur and long time spans after divergences for subsequent evolutionary changes to obscure the earlier ones. Another reason for difficulty in resolving some of the relationships using molecu- lar data is the limited spectrum of genes so far developed for phy- logeny estimation. For this latter issue, there is cause for current optimism owing to rapid increases in our knowledge of comparative genomics. -
Forest Fragmentation South Africa
Content Fragment quality rather than matrix habitat shapes forest regeneration in a South African mosaic-forest landscape Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften (Dr. rer. nat.) dem Fachbereich Biologie der vorgelegt von Diplom-Biologin Alexandra Botzat aus Frankfurt am Main Marburg an der Lahn, April 2012 Content 2 Content Vom Fachbereich Biologie der Philipps-Universität Marburg (Hochschulkennziffer: 1180) als Dissertation am 22.05.2012 angenommen. Dekan: Prof. Dr. Paul Galland Erstgutachterin: Jun.-Prof. Dr. Nina Farwig Zweitgutachter: Prof. Dr. Roland Brandl Tag der mündlichen Prüfung: 04.06.2012 Content 4 Content Saskia C. Morgenstern Content 6 Content ‘Humanity has always been, and always will be, a part of nature.’ (Gretchen C. Daily) Content Content 1 General introduction 1 Mosaic-forest landscapes 2 Rodent seed predation in mosaic-forest landscapes 3 Establishment of woody seedlings and saplings in mosaic-forest landscapes 4 Leaf damage of woody seedlings and saplings in mosaic-forest landscapes 6 Aims and outline of the thesis 7 2 Elevated seed predation in small forest fragments embedded in high- contrast matrices 9 Introduction 11 Methods 13 Results 19 Discussion 22 Conclusions 24 Acknowledgements 25 3 Late-successional tree recruits decrease in forest fragments with modified matrix habitat 27 Introduction 29 Methods 31 Results 35 Discussion 42 Conclusions 45 Acknowledgements 46 4 Forest fragment quality rather than matrix habitat shapes herbivory on tree recruits 47 Introduction 49 Methods 51 Results -
Dickel, T. S. 1991. New Records of Noctuid Moths from Florida
Vol. 2 No. 1 1991 DICKEL: Florida Noctuid Records 53 TROPICAL LEPIDOPTERA, 2(1): 53-58 NEW RECORDS OF NOCTUID MOTHS FROM FLORIDA (LEPIDOPTERA: NOCTUIDAE) TERHUNE S. DICKEL1 Box 385. Homestead, FL 33090, USA ABSTRACT.- New Florida records are reported for 30 species of Neotropical Noctuidae, with most of the new records also new for the continental United States fauna. KEY WORDS: Achaea, Aglaonice, Anacardiaceae, Anomis, Bleptina, Callopistria, Condica, distribution, Elaphria, Elousa, Epidromia, Eulepidotis, Euscirrhopterus, Gonodonta, hostplants, Hypena, Leucania, Litoprosopus, Macristis, Metalectra, Mimophisma, Mods, Myrtaceae, Neotuerta, Paectes, Pseudaletia, Ptichodis, Spodoptera, West Indies. This paper reports 30 species of Noctuidae collected in Florida, Dade Co.: Fuchs Hammock (Homestead) and Charles Deering primarily extreme southern Florida, of which 26 represent new Estate (Miami). Monroe Co.: Long Key St. Rec. Area, Bahia records for the continental United States. Most of these Neotrop- Honda St. Rec. Area, and N. Key Largo. Numerous records both ical species have not been illustrated previously and were not at MV light and at bait dating from 18 Jan 1985. Det. M. S. included in the North American MONA checklist (Hodges et al., Adams. 1983). Some of these species are now established in south Florida, particularly the Florida Keys and the Homestead, Dade 5. HYPENA SUBIDALIS Guenee Fig. 5 Co., area. One species, Metalectra geminicincta Schaus, de- Hypena subidalis Guenee, 1854. Brazil. scribed from Cuba and Mexico, is unusual in being established in Monroe Co.: Long Key St. Rec. Area, 18 Jan 1985 (1$); Bahia central and north Florida but as yet not recorded from south Honda St. Rec. -
Ecological Divergence and Speciation in Heliconius Cydno and H
Ecological divergence and speciation in Heliconius cydno and H. melpomene by Russell Edward Naisbit A thesis submitted for the degree of Doctor of Philosophy of the University of London September 2001 Department of Biology University College London To my family, for their support and encouragement throughout this crazy endeavour 2 “It is hardly an exaggeration to say, that whilst reading and reflecting on the various facts given in this Memoir, we feel to be as near witnesses, as we can ever hope to be, of the creation of a new species on this earth.” Charles Darwin, Natural History Review: Quarterly Journal of Biological Science, 1863. From a review of “Contributions to an Insect Fauna of the Amazon Valley,” in which Henry Walter Bates gave an adaptive explanation for mimicry in Amazonian butterflies and argued that variation in mimicry might cause speciation 3 Abstract We are in the midst of a renaissance in speciation research. There is a return to Darwin’s belief in the role of natural selection in driving speciation, after a lengthy focus on geographic isolation and hybrid sterility. Here I describe the ecological, behavioural, and genetic bases of speciation in Heliconius cydno and Heliconius melpomene (Lepidoptera: Nymphalidae). The two species are sympatric in tropical rainforest across most of Central America and the foothills of the Andes. Ecological differentiation allows coexistence of these sister species despite rare hybridisation. Divergence in microhabitat and larval host plant use has reduced both the potential for gene flow and for competition. In Panama H. cydno uses most Passiflora species in closed canopy forest, whilst H. -
A List of Cuban Lepidoptera (Arthropoda: Insecta)
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 3384: 1–59 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) A list of Cuban Lepidoptera (Arthropoda: Insecta) RAYNER NÚÑEZ AGUILA1,3 & ALEJANDRO BARRO CAÑAMERO2 1División de Colecciones Zoológicas y Sistemática, Instituto de Ecología y Sistemática, Carretera de Varona km 3. 5, Capdevila, Boyeros, Ciudad de La Habana, Cuba. CP 11900. Habana 19 2Facultad de Biología, Universidad de La Habana, 25 esq. J, Vedado, Plaza de La Revolución, La Habana, Cuba. 3Corresponding author. E-mail: rayner@ecologia. cu Table of contents Abstract . 1 Introduction . 1 Materials and methods. 2 Results and discussion . 2 List of the Lepidoptera of Cuba . 4 Notes . 48 Acknowledgments . 51 References . 51 Appendix . 56 Abstract A total of 1557 species belonging to 56 families of the order Lepidoptera is listed from Cuba, along with the source of each record. Additional literature references treating Cuban Lepidoptera are also provided. The list is based primarily on literature records, although some collections were examined: the Instituto de Ecología y Sistemática collection, Havana, Cuba; the Museo Felipe Poey collection, University of Havana; the Fernando de Zayas private collection, Havana; and the United States National Museum collection, Smithsonian Institution, Washington DC. One family, Schreckensteinidae, and 113 species constitute new records to the Cuban fauna. The following nomenclatural changes are proposed: Paucivena hoffmanni (Koehler 1939) (Psychidae), new comb., and Gonodontodes chionosticta Hampson 1913 (Erebidae), syn.