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Feature Saltation and the Evolution of Mimicry
ORIGINAL ARTICLE doi:10.1111/j.1558-5646.2011.01482.x FEATURE SALTATION AND THE EVOLUTION OF MIMICRY Gabriella Gamberale-Stille,1,2 Alexandra C. V. Balogh,1,3 Birgitta S. Tullberg,1 and Olof Leimar1,4 1Department of Zoology, Stockholm University, 10691 Stockholm, Sweden 2E-mail: [email protected] 3Environmental & Marine Biology, Abo˚ Akademi University, FIN-20520 Turku, Finland 4Wissenschaftskolleg zu Berlin, Wallotstrasse 19, 14193 Berlin, Germany Received May 27, 2011 Accepted September 26, 2011 In Batesian mimicry, a harmless prey species imitates the warning coloration of an unpalatable model species. A traditional suggestion is that mimicry evolves in a two-step process, in which a large mutation first achieves approximate similarity to the model, after which smaller changes improve the likeness. However, it is not known which aspects of predator psychology cause the initial mutant to be perceived by predators as being similar to the model, leaving open the question of how the crucial first step of mimicry evolution occurs. Using theoretical evolutionary simulations and reconstruction of examples of mimicry evolution, we show that the evolution of Batesian mimicry can be initiated by a mutation that causes prey to acquire a trait that is used by predators as a feature to categorize potential prey as unsuitable. The theory that species gain entry to mimicry through feature saltation allows us to formulate scenarios of the sequence of events during mimicry evolution and to reconstruct an initial mimetic appearance for important examples of Batesian mimicry. Because feature-based categorization by predators entails a qualitative distinction between nonmimics and passable mimics, the theory can explain the occurrence of imperfect mimicry. -
Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
Environmental Assessment Report Armenia: North-South Road
Environmental Assessment Report Environmental Impact Assessment (EIA) Document Stage: Draft Sub-project Number: 42145 August 2010 Armenia: North-South Road Corridor Investment Program Tranches 2 & 3 Prepared by Ministry of Transport and Communications (MOTC) of Armenia for Asian Development Bank The environmental impact assessment is a document of the borrower. The views expressed herein do not necessarily represent those of ADB’s Board of Directors, Management, or staff, and may be preliminary in nature. Armenia: North-South Road Corridor Investment Program Tranches 2 & 3 – Environmental Impact Assessment Report ABBREVIATIONS ADB Asian Development Bank AARM ADB Armenian Resident Mission CO2 carbon dioxide EA executing agency EARF environmental assessment and review framework EIA environmental impact assessment EMP environmental management and monitoring plan IUCN International Union for Conservation of Nature LARP Land Acquisition and Resettlement Plan MFF multi-tranche financing facility MNP Ministry of Nature Protection MOC Ministry of Culture MOH Ministry of Health MOTC Ministry of Transport and Communication NGO nongovernment organization NO2 nitrogen dioxide NO nitrogen oxide MPC maximum permissible concentration NPE Nature Protection Expertise NSS National Statistical Service PAHs polycyclic aromatic hydrocarbons PMU Project Management Unit PPTA Project Preparatory Technical Assistance RA Republic of Armenia RAMSAR Ramsar Convention on Wetlands REA Rapid Environmental Assessment (checklist) SEI State Environmental Inspectorate -
49370-002: National Power Grid Strengthening Project
Initial Environmental Examination Final Report Project No.: 49370-002 October 2020 Turkmenistan: National Power Grid Strengthening Project Volume 4 Prepared by the Ministry of Energy, Government of Turkmenistan for the Asian Development Bank. The Initial Environmental Examination is a document of the borrower. The views expressed herein do not necessarily represent those of ADB's Board of Directors, Management, or staff, and may be preliminary in nature. In preparing any country program or strategy, financing any project, or by making any designation of or reference to a particular territory or geographic area in this document, the Asian Development Bank does not intend to make any judgments as to the legal or other status of any territory or area. 49370-002: TKM TKM Power Sector Development Project 81. Out of these IBAs, eight IBAs are located close to phase I Transmission line alignments. Four IBAs are located close to proposed Gurtly (Ashgabat) to Balkanabat Transmission line. And four falls close to existing Sardar (West) to Dashoguz Transmission line. No IBA falls close to Dashoguz-Balkan Transmission line. The view of these IBAs with respect to transmission alignment of phase I are shown at Figure 4.17. 82. There are 8 IBAs along phase II alignment. Two IBAs, i.e. Lotfatabad & Darregaz and IBA Mergen is located at approx 6.0 km &approx 9.10 km from alignment respectively. The view of these IBAs with respect to transmission alignment of phase II is shown at Figure 4.18. : Presence of Important Bird Areas close to Proposed/existing -
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes Akito Y. Kawahara1*, Andre A. Mignault1, Jerome C. Regier2, Ian J. Kitching3, Charles Mitter1 1 Department of Entomology, College Park, Maryland, United States of America, 2 Center for Biosystems Research, University of Maryland Biotechnology Institute, College Park, Maryland, United States of America, 3 Department of Entomology, The Natural History Museum, London, United Kingdom Abstract Background: The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well- studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings: The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two- thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. -
The Mcguire Center for Lepidoptera and Biodiversity
Supplemental Information All specimens used within this study are housed in: the McGuire Center for Lepidoptera and Biodiversity (MGCL) at the Florida Museum of Natural History, Gainesville, USA (FLMNH); the University of Maryland, College Park, USA (UMD); the Muséum national d’Histoire naturelle in Paris, France (MNHN); and the Australian National Insect Collection in Canberra, Australia (ANIC). Methods DNA extraction protocol of dried museum specimens (detailed instructions) Prior to tissue sampling, dried (pinned or papered) specimens were assigned MGCL barcodes, photographed, and their labels digitized. Abdomens were then removed using sterile forceps, cleaned with 100% ethanol between each sample, and the remaining specimens were returned to their respective trays within the MGCL collections. Abdomens were placed in 1.5 mL microcentrifuge tubes with the apex of the abdomen in the conical end of the tube. For larger abdomens, 5 mL microcentrifuge tubes or larger were utilized. A solution of proteinase K (Qiagen Cat #19133) and genomic lysis buffer (OmniPrep Genomic DNA Extraction Kit) in a 1:50 ratio was added to each abdomen containing tube, sufficient to cover the abdomen (typically either 300 µL or 500 µL) - similar to the concept used in Hundsdoerfer & Kitching (1). Ratios of 1:10 and 1:25 were utilized for low quality or rare specimens. Low quality specimens were defined as having little visible tissue inside of the abdomen, mold/fungi growth, or smell of bacterial decay. Samples were incubated overnight (12-18 hours) in a dry air oven at 56°C. Importantly, we also adjusted the ratio depending on the tissue type, i.e., increasing the ratio for particularly large or egg-containing abdomens. -
British Lepidoptera (/)
British Lepidoptera (/) Home (/) Anatomy (/anatomy.html) FAMILIES 1 (/families-1.html) GELECHIOIDEA (/gelechioidea.html) FAMILIES 3 (/families-3.html) FAMILIES 4 (/families-4.html) NOCTUOIDEA (/noctuoidea.html) BLOG (/blog.html) Glossary (/glossary.html) Family: SPHINGIDAE (3SF 13G 18S) Suborder:Glossata Infraorder:Heteroneura Superfamily:Bombycoidea Refs: Waring & Townsend, Wikipedia, MBGBI9 Proboscis short to very long, unscaled. Antenna ~ 1/2 length of forewing; fasciculate or pectinate in male, simple in female; apex pointed. Labial palps long, 3-segmented. Eye large. Ocelli absent. Forewing long, slender. Hindwing ±triangular. Frenulum and retinaculum usually present but may be reduced. Tegulae large, prominent. Leg spurs variable but always present on midtibia. 1st tarsal segment of mid and hindleg about as long as tibia. Subfamily: Smerinthinae (3G 3S) Tribe: Smerinthini Probably characterised by a short proboscis and reduced or absent frenulum Mimas Smerinthus Laothoe 001 Mimas tiliae (Lime Hawkmoth) 002 Smerinthus ocellata (Eyed Hawkmoth) 003 Laothoe populi (Poplar Hawkmoth) (/002- (/001-mimas-tiliae-lime-hawkmoth.html) smerinthus-ocellata-eyed-hawkmoth.html) (/003-laothoe-populi-poplar-hawkmoth.html) Subfamily: Sphinginae (3G 4S) Rest with wings in tectiform position Tribe: Acherontiini Agrius Acherontia 004 Agrius convolvuli 005 Acherontia atropos (Convolvulus Hawkmoth) (Death's-head Hawkmoth) (/005- (/004-agrius-convolvuli-convolvulus- hawkmoth.html) acherontia-atropos-deaths-head-hawkmoth.html) Tribe: Sphingini Sphinx (2S) -
Butterflies and Moths of Yavapai County, Arizona, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Reptiles and Amphibians
A good book for beginners is Himmelman’s (2002) book “Discovering Moths’. Winter Moths (2000) describes several methods for By Dennis Skadsen capturing and observing moths including the use of light traps and sugar baits. There are Unlike butterflies, very little fieldwork has a few other essential books listed in the been completed to determine species suggested references section located on composition and distribution of moths in pages 8 & 9. Many moth identification northeast South Dakota. This is partly due guides can now be found on the internet, the to the fact moths are harder to capture and North Dakota and Iowa sites are the most study because most adults are nocturnal, and useful for our area. Since we often identification to species is difficult in the encounter the caterpillars of moths more field. Many adults can only be often than adults, having a guide like differentiated by studying specimens in the Wagners (2005) is essential. hand with a good understanding of moth taxonomy. Listed below are just a few of the species that probably occur in northeast South Although behavior and several physiological Dakota. The list is compiled from the characteristics separate moths from author’s personnel collection, and specimens butterflies including flight periods (moths collected by Gary Marrone or listed in Opler are mainly nocturnal (night) and butterflies (2006). Common and scientific names diurnal (day)); the shapes of antennae and follow Moths of North Dakota (2007) or wings; each have similar life histories. Both Opler (2006). moths and butterflies complete a series of changes from egg to adult called metamorphosis. -
Family Sphingidae
Caterpillar Biodiversity of the American Southwest David L. Wagner Dept. of Ecology & Evolutionary Biology University of Connecticut Larval Characteristics - usually cylindrical - six lateral ocelli - labial spinneret - spiracles on T1 and A1-A8. - segmented (true) legs on thoracic segments - prolegs on A3-A6 and A10 (although anterior prolegs often lost) (for speed walking) prolegs with crochets (hooks) - prothoracic shield on T1 - anal plate or shield on A10 Larval Chaetotaxy and Other Structures * primary setae homologous across groups * nomenclature for setal arrangement (chaetotaxy) standardized by Hinton (1946): often (2) dorsal, (2) subdorsal, (3) lateral, (1-3) subventral, and (1) ventral setae. Family-level Taxonomy * body proportions Figures from Stehr (1987) * chaetotaxy on body and head - presence of 2ndary setae - size and length of setae - branched or unbranched setae, etc., * crochets: arrangement and size heterogeneity * proleg number * glands * thoracic and anal plates Species-level Taxonomy * color patterns helpful for most external feeders (but not so for internal feeders) * chaetotaxy on body and head * ratio of frontal triangle to head height * hypopharyngeal complex * mandibular teeth * spiracular size and color * crochet numbers Accelerated (Phenotypic) Evolution in Larvae Elasmia packardii (Central Texas) Elasmia packardii Elasmia cave (West Texas) Elasmia cave Elasmia mandala (Arizona) Elasmia mandala wagneri Family Sphingidae * large, cylindrical body * setae inconspicuous except above prolegs * horn on dorsum -
The Sphingidae of Jordan: Distribution, Phenology & Ecology (Lepidoptera, Sphingidae) by G Unter C
©Ges. zur Förderung d. Erforschung von Insektenwanderungen e.V. München, download unter www.zobodat.at Atalanta (Juli 2005) 36 (1/2): 209-221, Würzburg, ISSN 0171-0079 The Sphingidae of Jordan: Distribution, Phenology & Ecology (Lepidoptera, Sphingidae) by G unter C. M üller 1, V asilyi K ravchenko 2, C huang L i', U lf E itschberger 3 M ichael A. M iller “1, O lga O rlova 2, W olfgang S peidel 5 & T homas W itt5 received 23.III.2005 |. department of Parasitology, Kuvin Centre for the Study of Infectious and Tropical Diseases, The Hebrew University - Hadassah-Medical School, Jerusalem, Israel. Department of Zoology, Tel Aviv University, Tel Aviv, Israel. V Entomologisches Museum E itschberger , Humboldstraße 13a, D-95168 Marktleuthen. T Zoologische Staatssammlung, Münchhausenstraße 23, D-81247 München. Museum W itt, Tengstr. 33, D-80796 München. Corresponding author: Dr. G. C. M üller : [email protected] Abstract: During a survey of seven years 21 Sphingid species belonging to 16 genera were collected in Jordan. Ten species were new records for the country [Acherontia styx styx (Westwood , 1848), Dolbina elegans A. B ang -H aas , 1912, Akbesia davidi (O berthür , 1884), Hemaris syra (D aniel , 1939), Hemaris molli E itschberger , M üller & K ravchenko , 2005, Hemaris croatica croatica croatica (E sper , 1800), Pterodonta gorgoniadespfeifferi (Z erny , 1933), Proserpinus proserpina proserpina (P allas , 1772), Hyles nicaea Hbanotica (G ehlen , 1932) and Rethera komarovi drilon R ebel & Z erny , 1932]. Some parasitic Tachainidae were recorded. The distribution, phenology, ecology, abundance and the association of all species to the main phyto-geographical zones of Jordan is discussed. -
Ts Denver Museum of Nature & Science Reports
DENVER MUSEUM OF NATURE & SCIENCE REPORTS DENVER MUSEUM OF NATURE & SCIENCE REPORTS DENVER MUSEUM OF NATURE & SCIENCE & SCIENCE OF NATURE DENVER MUSEUM NUMBER 16, OCTOBER 11, 2019 SCIENCE.DMNS.ORG/MUSEUM-PUBLICATIONS Denver Museum of Nature & Science Reports 2001 Colorado Boulevard (Print) ISSN 2374-7730 Denver, CO 80205, U.S.A. Denver Museum of Nature & Science Reports (Online) ISSN 2374-7749 REPORTS • NUMBER 16 • OCTOBER 11, 2019 • NUMBER 16 OCTOBER Cover photo: Oreas Anglewing (Polygonia oreas nigrozephyrus Scott, 1984), Gregory Canyon, Boulder County, Colorado, USA, 2 October 1973, leg. Michael G. Pogue. Photo: Bob Livingston. The Denver Museum of Nature & Science Reports (ISSN Frank Krell, PhD, Editor and Production 2374-7730 [print], ISSN 2374-7749 [online]) is an open- access, non peer-reviewed scientifi c journal publishing papers about DMNS research, collections, or other Program and Abstracts Museum related topics, generally authored or co-authored 30th Annual Meeting by Museum staff or associates. Peer review will only be arranged on request of the authors. of the High Country Lepidopterists October 11–12, 2019 The journal is available online at science.dmns.org/ Museum-Publications free of charge. Paper copies Denver Museum of Nature & Science are available for purchase from our print-on-demand publisher Lulu (www.lulu.com). DMNS owns the copyright of the works published in the Reports, which are Frank-Thorsten Krell (Ed.) published under the Creative Commons Attribution Non- Commercial license. For commercial use of published