Chapter 7 SOUTH AMERICA
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Mitt. Münch. Ent. Ges. 106 Suppl. S2 1-10 München, 15.02.2016 Systematische, revidierte und kommentierte Checkliste der Schmetterlinge Bayerns (Insecta: Lepidoptera) Alfred HASLBERGER & Andreas H. SEGERER Supplementmaterial S2 Zusammenstellung der in vorliegender Arbeit publizierten regionalen Neu- und Wiederfunde. S2.1 Neufunde für die Bayerischen Alpen und/oder das Alpenvorland (AVA) Nr. FauEu Überfamilie Familie Art 0016 431725 Eriocranioidea Eriocraniidae Dyseriocrania subpurpurella (HAWORTH, 1828) 0026 431739 Eriocranioidea Eriocraniidae Eriocrania semipurpurella (STEPHENS, 1835) 0058 431808 Nepticuloidea Nepticulidae Stigmella aceris (FREY, 1857) 0080 431900 Nepticuloidea Nepticulidae Stigmella myrtillella (STAINTON, 1857) 0089 431932 Nepticuloidea Nepticulidae Stigmella splendidissimella (HERRICH-SCHÄFFER, 1855) 0125 432021 Nepticuloidea Nepticulidae Ectoedemia decentella (HERRICH-SCHÄFFER, 1855) 0133 432060 Nepticuloidea Nepticulidae Ectoedemia hannoverella (GLITZ, 1872) 0158 432282 Adeloidea Heliozelidae Heliozela resplendella (STAINTON, 1851) 0182 432335 Adeloidea Adelidae Adela cuprella (DENIS & SCHIFFERMÜLLER, 1775) 0202 432387 Adeloidea Incurvariidae Incurvaria pectinea HAWORTH, 1828 0230 432437 Tischerioidea Tischeriidae Coptotriche marginea (HAWORTH, 1828) 0331 433122 Tineoidea Tineidae Nemapogon granella (LINNAEUS, 1758) 0355 432916 Tineoidea Tineidae Monopis weaverella (SCOTT, 1858) 0371 433010 Tineoidea Tineidae Tinea columbariella WOCKE, 1877 0373 433015 Tineoidea Tineidae Tinea trinotella THUNBERG, 1794 0394 433489 -
Lepidoptera on the Introduced Robinia Pseudoacacia in Slovakia, Central Europe
Check List 8(4): 709–711, 2012 © 2012 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution Lepidoptera on the introduced Robinia pseudoacacia in PECIES S OF ISTS L Slovakia, Central Europe Miroslav Kulfan E-mail: [email protected] Comenius University, Faculty of Natural Sciences, Department of Ecology, Mlynská dolina B-1, SK-84215 Bratislava, Slovakia. Abstract: Robinia pseudoacacia A current checklist of Lepidoptera that utilize as a hostplant in Slovakia (Central Europe) faunalis provided. community. The inventory Two monophagous is based on species, a bibliographic the leaf reviewminers andMacrosaccus new unreported robiniella data and from Parectopa southwest robiniella Slovakia., and Thethe polyphagouslist includes 35pest Lepidoptera Hyphantria species cunea belonging to 10 families. Most species are polyphagous and belong to Euro-Siberian have subsequently been introduced to Slovakia. Introduction E. The area is a polygon enclosed by the towns of Bratislava, Robinia pseudoacacia a widespread species in its native habitat in southeastern North America. It was L.introduced (black locust, to orEurope false acacia),in 1601 is Komárno, Veľký Krtíš and Myjava. Ten plots were located in the southern part of the study area. Most were located in theThe remnant trophic ofgroups the original of the floodplain Lepidoptera forests larvae that found were (Chapman 1935). The first mention of planting the species distributed along the Danube and Morava rivers. (Keresztesiin Slovakia dates 1965). from Today, 1750, itwhen is widespread black locust wasthroughout planted (1986). The zoogeographical distribution of the species western,around the central, fortress eastern in Komárno and southern in southern Europe, Slovakia where followswere defined the arrangement following the give system by Reiprichof Brown (2001). -
Lepidoptera of Albany Hill, Alameda Co., California
LEPIDOPTERA OF ALBANY HILL, ALAMEDA CO., CALIFORNIA Jerry A. Powell Essig Museum of Entomology University of California, Berkeley and Robert L. Langston Kensington, CA November 1999; edited 2009 The following list summarizes observations of Lepidoptera (moths and butterflies) at Albany Hill, Alameda Co., California, during 1995-1999. Data originate from about 75 daytime and crepuscular visits of 0.5 to 3.5 hrs, in all months of the year. All of the butterfly species and some of the moths were recorded by RLL, most of the moth species and their larval host plants by JAP. A total of 145 species is recorded (30 butterflies, 115 moths), a modest number considering the extent and diversity of the flora. However, many of the potential larval host plants may be present in too small patches to support populations of larger moths or butterflies. Nonetheless, we were surprised that colonies of some of the species survive in a small area that has been surrounded by urban development for many decades, including some rare ones in the East Bay region, as annotated below. Moreover, the inventory is incomplete. A more comprehensive census would be accomplished by trapping moths attracted to ultraviolet lights. In a habitat of this size, however, such survey would attract an unknown proportion of species from surrounding areas. Larval collections are indicated by date-based JAP lot numbers (e.g. 95C37 = 1995, March, 37th collection). Larval foods of most of the other species are documented in other populations. Host plants are recorded at Albany Hill for 75 species (65% of the moths, 52% of the total); the rest were observed as adults only. -
FIELD OBSERVATIONS of TROPIDACRIS COLLARIS (ORTHOPTERA: ROMALEIDAE) Christopher K
FIELD OBSERVATIONS OF TROPIDACRIS COLLARIS (ORTHOPTERA: ROMALEIDAE) Christopher K. Starr Dep't of Life Sciences, University of the West Indies,St Augustine, Trinidad & 'Ibbago cstarr{jj}centre.uwi.tt Tropidacris i s a neotropi c al genus of three known s peci es aggregation close to the ground on a small shrub c lose along that include the largest g r asshoppers in the world (Carbone ll side the gulch. I netted a sampl e of these, which disturbance 19 86). Two species, T. collaris and T. crisrata, have very caused the remai nin g individuals to scatter. Some time later broad ranges that include mos t of South America north of the I returned to that spot and found th e aggregation re-formed southern cone . The former is the species found on Margarita in a s imilar s ituation less than a meter from where I had first Is land, wh il e the range of the latter inc ludes Tri nidad and found it. Although I did not attempt to quantify ad ult densi Tobago. The two are readily distingui s hed by the fo llowing ty in any part of the gulch, they appeared to be most concen adult characters (Carbonell 1984.1986): a) a nte nnae enti rely trated within a very few meters of the aggregation of hoppers. yellow in T. collaris, basal two segments brown to black in T. I tas ted one hopper and found it to be very biller. approx cristata, b) dorsa l crest of pronotum continu ing o nto posteri imately like an adu lt mo narch butterfly (Danaus plexippus). -
Insect Classification Standards 2020
RECOMMENDED INSECT CLASSIFICATION FOR UGA ENTOMOLOGY CLASSES (2020) In an effort to standardize the hexapod classification systems being taught to our students by our faculty in multiple courses across three UGA campuses, I recommend that the Entomology Department adopts the basic system presented in the following textbook: Triplehorn, C.A. and N.F. Johnson. 2005. Borror and DeLong’s Introduction to the Study of Insects. 7th ed. Thomson Brooks/Cole, Belmont CA, 864 pp. This book was chosen for a variety of reasons. It is widely used in the U.S. as the textbook for Insect Taxonomy classes, including our class at UGA. It focuses on North American taxa. The authors were cautious, presenting changes only after they have been widely accepted by the taxonomic community. Below is an annotated summary of the T&J (2005) classification. Some of the more familiar taxa above the ordinal level are given in caps. Some of the more important and familiar suborders and families are indented and listed beneath each order. Note that this is neither an exhaustive nor representative list of suborders and families. It was provided simply to clarify which taxa are impacted by some of more important classification changes. Please consult T&J (2005) for information about taxa that are not listed below. Unfortunately, T&J (2005) is now badly outdated with respect to some significant classification changes. Therefore, in the classification standard provided below, some well corroborated and broadly accepted updates have been made to their classification scheme. Feel free to contact me if you have any questions about this classification. -
1 Appendix 3. Gulf Islands Taxonomy Report
Appendix 3. Gulf Islands Taxonomy Report Class Order Family Genus Species Arachnida Araneae Agelenidae Agelenopsis Agelenopsis utahana Eratigena Eratigena agrestis Amaurobiidae Callobius Callobius pictus Callobius severus Antrodiaetidae Antrodiaetus Antrodiaetus pacificus Anyphaenidae Anyphaena Anyphaena aperta Anyphaena pacifica Araneidae Araneus Araneus diadematus Clubionidae Clubiona Clubiona lutescens Clubiona pacifica Clubiona pallidula Cybaeidae Cybaeus Cybaeus reticulatus Cybaeus signifer Cybaeus tetricus Dictynidae Emblyna Emblyna peragrata Gnaphosidae Sergiolus Sergiolus columbianus Zelotes Zelotes fratris Linyphiidae Agyneta Agyneta darrelli Agyneta fillmorana Agyneta protrudens Bathyphantes Bathyphantes brevipes Bathyphantes keeni 1 Centromerita Centromerita bicolor Ceratinops Ceratinops latus Entelecara Entelecara acuminata Erigone Erigone aletris Erigone arctica Erigone cristatopalpus Frederickus Frederickus coylei Grammonota Grammonota kincaidi Linyphantes Linyphantes nehalem Linyphantes nigrescens Linyphantes pacificus Linyphantes pualla Linyphantes victoria Mermessus Mermessus trilobatus Microlinyphia Microlinyphia dana Neriene Neriene digna Neriene litigiosa Oedothorax Oedothorax alascensis Pityohyphantes Pityohyphantes alticeps Pocadicnemis Pocadicnemis pumila Poeciloneta Poeciloneta fructuosa Saaristoa Saaristoa sammamish Scotinotylus Scotinotylus sp. 5GAB Semljicola Semljicola sp. 1GAB Sisicottus Spirembolus Spirembolus abnormis Spirembolus mundus Tachygyna Tachygyna ursina Tachygyna vancouverana Tapinocyba Tapinocyba -
In the Dark in a Large Urban Park: DNA Barcodes Illuminate Cryptic and Introduced Moth Species
Biodivers Conserv DOI 10.1007/s10531-009-9682-7 ORIGINAL PAPER In the dark in a large urban park: DNA barcodes illuminate cryptic and introduced moth species Jeremy R. deWaard Æ Jean-Franc¸ois Landry Æ B. Christian Schmidt Æ Jennifer Derhousoff Æ John A. McLean Æ Leland M. Humble Received: 3 November 2008 / Accepted: 18 June 2009 Ó Springer Science+Business Media B.V. 2009 Abstract To facilitate future assessments of diversity following disturbance events, we conducted a first level inventory of nocturnal Lepidoptera in Stanley Park, Vancouver, Canada. To aid the considerable task, we employed high-throughput DNA barcoding for the rough sorting of all material and for tentative species identifications, where possible. We report the preliminary species list of 190, the detection of four new exotic species (Argyresthia pruniella, Dichelia histrionana, Paraswammerdamia lutarea, and Prays fraxinella), and the potential discovery of two cryptic species. We describe the magnitude of assistance that barcoding presents for faunal inventories, from reducing specialist time to facilitating the detection of native and exotic species at low density. Electronic supplementary material The online version of this article (doi:10.1007/s10531-009-9682-7) contains supplementary material, which is available to authorized users. J. R. deWaard (&) Á J. Derhousoff Á J. A. McLean Á L. M. Humble Department of Forest Sciences, Forestry Sciences Centre, University of British Columbia, Vancouver, BC V6T 1Z4, Canada e-mail: [email protected] J. R. deWaard Royal British Columbia Museum, Entomology, 675 Belleville Street, Victoria, BC V8W 9W2, Canada J.-F. Landry Agriculture and Agri-Food Canada, Canadian National Collection of Insects, Arachnids and Nematodes, K.W. -
Spreading of Heterochromatin and Karyotype Differentiation in Two Tropidacris Scudder, 1869 Species (Orthoptera, Romaleidae)
COMPARATIVE A peer-reviewed open-access journal CompCytogen 9(3): 435–450 (2015)Spreading of heterochromatin in Tropidacris 435 doi: 10.3897/CompCytogen.v9i3.5160 RESEARCH ARTICLE Cytogenetics http://compcytogen.pensoft.net International Journal of Plant & Animal Cytogenetics, Karyosystematics, and Molecular Systematics Spreading of heterochromatin and karyotype differentiation in two Tropidacris Scudder, 1869 species (Orthoptera, Romaleidae) Marília de França Rocha1, Mariana Bozina Pine2, Elizabeth Felipe Alves dos Santos Oliveira3, Vilma Loreto3, Raquel Bozini Gallo2, Carlos Roberto Maximiano da Silva2, Fernando Campos de Domenico4, Renata da Rosa2 1 Departamento de Biologia, ICB, Universidade de Pernambuco, Recife, Pernambuco, Brazil 2 Departamento de Biologia Geral, CCB, Universidade Estadual de Londrina (UEL), Londrina, Paraná, Brazil 3 Depar- tamento de Genética, CCB, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil 4 Museu de Zoologia, Instituto de Biociência, Universidade de São Paulo, São Paulo, São Paulo, Brazil Corresponding author: Renata da Rosa ([email protected]) Academic editor: V. Gokhman | Received 22 April 2015 | Accepted 5 June 2015 | Published 24 July 2015 http://zoobank.org/12E31847-E92E-41AA-8828-6D76A3CFF70D Citation: Rocha MF, Pine MB, dos Santos Oliveira EFA, Loreto V, Gallo RB, da Silva CRM, de Domenico FC, da Rosa R (2015) Spreading of heterochromatin and karyotype differentiation in twoTropidacris Scudder, 1869 species (Orthoptera, Romaleidae). Comparative Cytogenetics 9(3): 435–450. doi: 10.3897/CompCytogen.v9i3.5160 Abstract Tropidacris Scudder, 1869 is a genus widely distributed throughout the Neotropical region where specia- tion was probably promoted by forest reduction during the glacial and interglacial periods. There are no cytogenetic studies of Tropidacris, and information allowing inference or confirmation of the evolutionary events involved in speciation within the group is insufficient. -
The Isabella Plantation Conservation Management Plan February 2012
The Isabella Plantation Conservation Management Plan February 2012 Isabella Plantation Landscape Conservation Management Plan 2012 Prepared by The Royal Parks January 2012 The Royal Parks Rangers Lodge Hyde Park London W2 2UH Tel: 020 7298 2000 Fax: 020 7402 3298 [email protected] i Isabella Plantation Conservation Management Plan CONTENTS 1.0 INTRODUCTION .............................................................................. 3 Richmond Park ............................................................................................................................................. 3 The Management Plan ................................................................................................................................ 4 Aims of the Isabella Plantation Management Plan ................................................................................ 4 Structure of the Plan .................................................................................................................................. 6 2.0 GENERAL AND MANAGEMENT CONTEXT ............................... 7 Location ......................................................................................................................................................... 7 Existing TRP Management Framework ................................................................................................ 10 Management Structure of Richmond Park .......................................................................................... 10 Landscape Management -
New Canadian and Ontario Orthopteroid Records, and an Updated Checklist of the Orthoptera of Ontario
Checklist of Ontario Orthoptera (cont.) JESO Volume 145, 2014 NEW CANADIAN AND ONTARIO ORTHOPTEROID RECORDS, AND AN UPDATED CHECKLIST OF THE ORTHOPTERA OF ONTARIO S. M. PAIERO1* AND S. A. MARSHALL1 1School of Environmental Sciences, University of Guelph, Guelph, Ontario, Canada N1G 2W1 email, [email protected] Abstract J. ent. Soc. Ont. 145: 61–76 The following seven orthopteroid taxa are recorded from Canada for the first time: Anaxipha species 1, Cyrtoxipha gundlachi Saussure, Chloroscirtus forcipatus (Brunner von Wattenwyl), Neoconocephalus exiliscanorus (Davis), Camptonotus carolinensis (Gerstaeker), Scapteriscus borellii Linnaeus, and Melanoplus punctulatus griseus (Thomas). One further species, Neoconocephalus retusus (Scudder) is recorded from Ontario for the first time. An updated checklist of the orthopteroids of Ontario is provided, along with notes on changes in nomenclature. Published December 2014 Introduction Vickery and Kevan (1985) and Vickery and Scudder (1987) reviewed and listed the orthopteroid species known from Canada and Alaska, including 141 species from Ontario. A further 15 species have been recorded from Ontario since then (Skevington et al. 2001, Marshall et al. 2004, Paiero et al. 2010) and we here add another eight species or subspecies, of which seven are also new Canadian records. Notes on several significant provincial range extensions also are given, including two species originally recorded from Ontario on bugguide.net. Voucher specimens examined here are deposited in the University of Guelph Insect Collection (DEBU), unless otherwise noted. New Canadian records Anaxipha species 1 (Figs 1, 2) (Gryllidae: Trigidoniinae) This species, similar in appearance to the Florida endemic Anaxipha calusa * Author to whom all correspondence should be addressed. -
Wing-Based Communication in Carboniferous Insects
ARTICLE https://doi.org/10.1038/s42003-021-02281-0 OPEN Sound vs. light: wing-based communication in Carboniferous insects ✉ Thomas Schubnel 1,5 , Frédéric Legendre 1,5, Patrick Roques2, Romain Garrouste1, Raphaël Cornette1, ✉ Michel Perreau3,4, Naïl Perreau4, Laure Desutter-Grandcolas1,5 & André Nel 1,5 Acoustic communication is well-known in insects since the Mesozoic, but earlier evidence of this behavior is rare. Titanoptera, an ‘orthopteroid’ Permian-Triassic order, is one of the few candidates for Paleozoic intersex calling interactions: some specimens had highly specialized broadened zones on the forewings, which are currently considered—despite inconclusive evidence—as ‘resonators’ of a stridulatory apparatus. Here we argue that the stridulatory 1234567890():,; apparatus hypothesis is unlikely because the Titanoptera lack a stridulatory file on their bodies, legs or wings. Instead, comparing these broadened zones with similar structures in extant locusts, flies, and fossil damselflies, we find evidence that the Titanoptera used their wings to produce flashes of light and/or crepitated sounds. Moreover, we describe the first Carboniferous (~310 Mya) Titanoptera, which exhibits such specialized zones, thus corre- sponding to the oldest record of wing communication in insects. Whether these commu- nication systems were used to attract sexual partners and/or escape predators remain to be demonstrated. 1 Institut de Systématique, Évolution, Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, Paris Cedex 05, France. 2 Allée des Myosotis, Neuilly sur Marne, France. 3 IUT Paris Diderot, Université de Paris, 20 quater rue du département, Paris, France. 4 27 quai d’Anjou, Paris, France. 5These authors contributed equally: Thomas Schubnel, Frédéric Legendre, Laure Desutter-Grandcolas, André Nel. -
The Significance of Body Size in the Orthoptera: a Review
DOUGLAS W. WHITMANJournal of Orthoptera Research 2008,17(2): 117-134117 The significance of body size in the Orthoptera: a review DOUGLAS W. WHITMAN 4120 Department of Biological Sciences, Illinois State University, Normal, IL 61790, USA. Email: [email protected] Abstract Why size and mass are important This review discusses body size and mass as they relate to the Orthoptera Size and mass are important because they correlate strongly (crickets, katydids, grasshoppers) and the Phasmatodea (walkingsticks). It with fitness, because they directly or indirectly influence nearly all addresses the expression, causes and consequences of size in these insects. biological phenomena, and because a great many biological and Topics include: methodological problems in body-size research, gravity physical factors influence size and mass. As such, size and mass vs surface forces, allometry and scaling, Dyar’s law, ontogenetic scaling, are determinants of fitness and targets of natural selection. For size-invariant traits and nonallometric scaling, the influence of size on researchers, size and mass are two easily obtained values that can physiology, function, behavior, life history, mating, fecundity, population encapsulate and predict a multitude of more difficult-to-obtain dynamics, ecology, and community, size-clines, Bergmann’s rule, sexual variables, such as metabolic rate, physiological condition, stress- size dimorphism, Rensch’s rule, protandry, the environmental, genetic, and resistance, immunocompetency, locomotor and dispersal abilities, physiological control of size, the evolution of size and the influence of size fecundity, life history, mating system and mating success, abundance, on evolution. Hypotheses are presented to explain why insects remain small in comparison to other taxa.