Insecta, Apterygota
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The Mitochondrial Genomes of Palaeopteran Insects and Insights
www.nature.com/scientificreports OPEN The mitochondrial genomes of palaeopteran insects and insights into the early insect relationships Nan Song1*, Xinxin Li1, Xinming Yin1, Xinghao Li1, Jian Yin2 & Pengliang Pan2 Phylogenetic relationships of basal insects remain a matter of discussion. In particular, the relationships among Ephemeroptera, Odonata and Neoptera are the focus of debate. In this study, we used a next-generation sequencing approach to reconstruct new mitochondrial genomes (mitogenomes) from 18 species of basal insects, including six representatives of Ephemeroptera and 11 of Odonata, plus one species belonging to Zygentoma. We then compared the structures of the newly sequenced mitogenomes. A tRNA gene cluster of IMQM was found in three ephemeropteran species, which may serve as a potential synapomorphy for the family Heptageniidae. Combined with published insect mitogenome sequences, we constructed a data matrix with all 37 mitochondrial genes of 85 taxa, which had a sampling concentrating on the palaeopteran lineages. Phylogenetic analyses were performed based on various data coding schemes, using maximum likelihood and Bayesian inferences under diferent models of sequence evolution. Our results generally recovered Zygentoma as a monophyletic group, which formed a sister group to Pterygota. This confrmed the relatively primitive position of Zygentoma to Ephemeroptera, Odonata and Neoptera. Analyses using site-heterogeneous CAT-GTR model strongly supported the Palaeoptera clade, with the monophyletic Ephemeroptera being sister to the monophyletic Odonata. In addition, a sister group relationship between Palaeoptera and Neoptera was supported by the current mitogenomic data. Te acquisition of wings and of ability of fight contribute to the success of insects in the planet. -
A New Insect Trackway from the Upper Jurassic—Lower Cretaceous Eolian Sandstones of São Paulo State, Brazil: Implications for Reconstructing Desert Paleoecology
A new insect trackway from the Upper Jurassic—Lower Cretaceous eolian sandstones of São Paulo State, Brazil: implications for reconstructing desert paleoecology Bernardo de C.P. e M. Peixoto1,2, M. Gabriela Mángano3, Nicholas J. Minter4, Luciana Bueno dos Reis Fernandes1 and Marcelo Adorna Fernandes1,2 1 Laboratório de Paleoicnologia e Paleoecologia, Departamento de Ecologia e Biologia Evolutiva, Universidade Federal de São Carlos (UFSCar), São Carlos, São Paulo, Brazil 2 Programa de Pós Graduacão¸ em Ecologia e Recursos Naturais, Centro de Ciências Biológicas e da Saúde, Universidade Federal de São Carlos (UFSCar), São Carlos, São Paulo, Brazil 3 Department of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada 4 School of the Environment, Geography, and Geosciences, University of Portsmouth, Portsmouth, Hampshire, United Kingdom ABSTRACT The new ichnospecies Paleohelcura araraquarensis isp. nov. is described from the Upper Jurassic-Lower Cretaceous Botucatu Formation of Brazil. This formation records a gigantic eolian sand sea (erg), formed under an arid climate in the south-central part of Gondwana. This trackway is composed of two track rows, whose internal width is less than one-quarter of the external width, with alternating to staggered series, consisting of three elliptical tracks that can vary from slightly elongated to tapered or circular. The trackways were found in yellowish/reddish sandstone in a quarry in the Araraquara municipality, São Paulo State. Comparisons with neoichnological studies and morphological inferences indicate that the producer of Paleohelcura araraquarensis isp. nov. was most likely a pterygote insect, and so could have fulfilled one of the Submitted 6 November 2019 ecological roles that different species of this group are capable of performing in dune Accepted 10 March 2020 deserts. -
Insecta: Phasmatodea) and Their Phylogeny
insects Article Three Complete Mitochondrial Genomes of Orestes guangxiensis, Peruphasma schultei, and Phryganistria guangxiensis (Insecta: Phasmatodea) and Their Phylogeny Ke-Ke Xu 1, Qing-Ping Chen 1, Sam Pedro Galilee Ayivi 1 , Jia-Yin Guan 1, Kenneth B. Storey 2, Dan-Na Yu 1,3 and Jia-Yong Zhang 1,3,* 1 College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China; [email protected] (K.-K.X.); [email protected] (Q.-P.C.); [email protected] (S.P.G.A.); [email protected] (J.-Y.G.); [email protected] (D.-N.Y.) 2 Department of Biology, Carleton University, Ottawa, ON K1S 5B6, Canada; [email protected] 3 Key Lab of Wildlife Biotechnology, Conservation and Utilization of Zhejiang Province, Zhejiang Normal University, Jinhua 321004, China * Correspondence: [email protected] or [email protected] Simple Summary: Twenty-seven complete mitochondrial genomes of Phasmatodea have been published in the NCBI. To shed light on the intra-ordinal and inter-ordinal relationships among Phas- matodea, more mitochondrial genomes of stick insects are used to explore mitogenome structures and clarify the disputes regarding the phylogenetic relationships among Phasmatodea. We sequence and annotate the first acquired complete mitochondrial genome from the family Pseudophasmati- dae (Peruphasma schultei), the first reported mitochondrial genome from the genus Phryganistria Citation: Xu, K.-K.; Chen, Q.-P.; Ayivi, of Phasmatidae (P. guangxiensis), and the complete mitochondrial genome of Orestes guangxiensis S.P.G.; Guan, J.-Y.; Storey, K.B.; Yu, belonging to the family Heteropterygidae. We analyze the gene composition and the structure D.-N.; Zhang, J.-Y. -
ENTOMOLOGY 322 LABS 13 & 14 Insect Mouthparts
ENTOMOLOGY 322 LABS 13 & 14 Insect Mouthparts The diversity in insect mouthparts may explain in part why insects are the predominant form of multicellular life on earth (Bernays, 1991). Insects, in one form or another, consume essentially every type of food on the planet, including most terrestrial invertebrates, plant leaves, pollen, fungi, fungal spores, plant fluids (both xylem and phloem), vertebrate blood, detritus, and fecal matter. Mouthparts are often modified for other functions as well, including grooming, fighting, defense, courtship, mating, and egg manipulation. This tremendous morphological diversity can tend to obscure the essential appendiculate nature of insect mouthparts. In the following lab exercises we will track the evolutionary history of insect mouthparts by comparing the mouthparts of a generalized insect (the cricket you studied in the last lab) to a variety of other arthropods, and to the mouthparts of some highly modified insects, such as bees, butterflies, and cicadas. As mentioned above, the composite nature of the arthropod head has lead to considerable debate as to the true homologies among head segments across the arthropod classes. Table 13.1 is presented below to help provide a framework for examining the mouthparts of arthropods as a whole. 1. Obtain a specimen of a horseshoe crab (Merostoma: Limulus), one of the few extant, primitively marine Chelicerata. From dorsal view, note that the body is divided into two tagmata, the anterior Figure 13.1 (Brusca & Brusca, 1990) prosoma (cephalothorax) and the posterior opisthosoma (abdomen) with a caudal spine (telson) at its end (Fig. 13.1). In ventral view, note that all locomotory and feeding appendages are located on the prosoma and that all except the last are similar in shape and terminate in pincers. -
Insect Life Histories and Diversity Outline HOW MANY SPECIES OF
Insect Life Histories and Diversity Outline 1. There are many kinds of insects 2. Why, how? 3. The Orders HOW MANY SPECIES OF INSECTS ARE THERE? Insect Diversity • Distribution spread primarily between 5 orders 1. Coleoptera (beetles) = 350,000 2. Lepidoptera (butterflies and moths) = 150,000 3. Hymenoptera (wasps, ants and bees) = 125,000 4. Diptera (flies) = 120,000 5. Hemiptera (bugs etc) =90,000 1 There has never been more insect diversity than now WHY DO INSECTS DOMINATE THE NUMBER OF SPECIES? 540 Why? Insects were the first animals to • Insects have been around over 400 million years adapt to and diversify on land First insect fossils Land becomes habitable Why is the basis of Why? high rates of speciation? • Their geologic age • High speciation rates • High fecundity (many offspring) • Short generation time (more chances • One estimate: Lepidoptera for mutation) in the last 100 million years added 2-3 species • These combine to produce huge # of every thousand years individuals, increased range of variation • = more variation for natural selection 2 Combined with low rates of natural Why? extinction • Geologic age • Fossil evidence • Capacity for high speciation rates that insects • Low rates of extinction were not affected (much) by • Design previous mass extinction events •Why? DESIGN Insect Size –size and life span Wide range of insect sizes.... –diversity of characteristics of insect cuticle –flight –modularity at many levels –holometabolous larvae But most are small 3 Small size Life Span • Wide variation 1. Shorter generation time 2. More ecological niches available than to larger animals Life Span • Wide variation but most are relatively short insect cuticle Flight • Takes on diversity of shapes, colors, textures • A composite material: variations are tough enough to cut hardwood, have high plasticity, delicate enough gases will diffuse through it. -
Sistemática Y Ecología De Las Hormigas Predadoras (Formicidae: Ponerinae) De La Argentina
UNIVERSIDAD DE BUENOS AIRES Facultad de Ciencias Exactas y Naturales Sistemática y ecología de las hormigas predadoras (Formicidae: Ponerinae) de la Argentina Tesis presentada para optar al título de Doctor de la Universidad de Buenos Aires en el área CIENCIAS BIOLÓGICAS PRISCILA ELENA HANISCH Directores de tesis: Dr. Andrew Suarez y Dr. Pablo L. Tubaro Consejero de estudios: Dr. Daniel Roccatagliata Lugar de trabajo: División de Ornitología, Museo Argentino de Ciencias Naturales “Bernardino Rivadavia” Buenos Aires, Marzo 2018 Fecha de defensa: 27 de Marzo de 2018 Sistemática y ecología de las hormigas predadoras (Formicidae: Ponerinae) de la Argentina Resumen Las hormigas son uno de los grupos de insectos más abundantes en los ecosistemas terrestres, siendo sus actividades, muy importantes para el ecosistema. En esta tesis se estudiaron de forma integral la sistemática y ecología de una subfamilia de hormigas, las ponerinas. Esta subfamilia predomina en regiones tropicales y neotropicales, estando presente en Argentina desde el norte hasta la provincia de Buenos Aires. Se utilizó un enfoque integrador, combinando análisis genéticos con morfológicos para estudiar su diversidad, en combinación con estudios ecológicos y comportamentales para estudiar la dominancia, estructura de la comunidad y posición trófica de las Ponerinas. Los resultados sugieren que la diversidad es más alta de lo que se creía, tanto por que se encontraron nuevos registros durante la colecta de nuevo material, como porque nuestros análisis sugieren la presencia de especies crípticas. Adicionalmente, demostramos que en el PN Iguazú, dos ponerinas: Dinoponera australis y Pachycondyla striata son componentes dominantes en la comunidad de hormigas. Análisis de isótopos estables revelaron que la mayoría de las Ponerinas ocupan niveles tróficos altos, con excepción de algunas especies arborícolas del género Neoponera que dependerían de néctar u otros recursos vegetales. -
Insecta, Apterygota, Microcoryphia)
Miscel.lania Zoologica 20.1 (1997) 119 The antennal basiconic sensilla and taxonomy of Machilinus Silvestri, 1904 (Insecta, Apterygota, Microcoryphia) M. J. Notario-Muñoz, C. Bach de Roca, R. Molero-Baltanás & M. Gaju-Ricart Notario-Muñoz, M. J., Bach de Roca, C., Molero-Baltanás, R. & Gaju-Ricart, M., 1997. The antennal basiconic sensilla and taxonomy of Machilinus Silvestri, 1904 (Insecta, Apterygota, Microcoryphia). Misc. ZOO~.,20.1: 119-123. The antennal basiconic sensilla and taxonomy of Machilinus Silvestri, 1904 (Insecta, Apterygota, Microcoryphia).- Some special antennal sensilla ('rosettenformige' and basiconica) of five species of Mach~fihus(Mei nertellidae): M. casasecai, M. helicopalpus, M. kleinenbergi, M. rupestris gallicus and M. spinifrontis were studied. The distribution patterns of the sensilla are different for each examined species and identical in both sexes. The sensillogram thus provides a good taxonomic characteristic for their identification. Key words: Taxonomy, Antennal sensilla, Basiconic sensilla, Machilinus. (Rebut: 8 VI1 96; Acceptació condicional: 4 XI 96; Acc. definitiva: 17 XII 96) María José Notario-Muñoz, Rafael Molero-Baltanás & Miguel Gaju-Ricart, Depto. de Biología Animal (Zoología), Univ. Córdoba, 14005 Córdoba, España (Spain).- Carmen Bach de Roca, Depto. de Biología Animal, Vegetal y Ecología, Univ. Autónoma de Barcelona, Bellaterra 08193, Barcelona, España (Spain). l This work was supported by Fauna Ibérica III SEUI-DGICYT PB92-0121. O 1997 Museu de Zoologia Notario-Muñoz et al. lntroduction M. casasecai Bach, 1974, 8 88 y 2 99, Lérida (Spain) 28 V 86; M. spinifrontis Bach, The insects' antennae are provided with 1984, 4 88' y 5 99, Jaén (Spain) 11 VI1 82 specialized sensilla which function, rnainly, and 10 X 82. -
From Dryland and Inundation Forests of Central Amazonia
AMAZONIANA X 2 197 - 218 Kiel, Oktober 1987 From cooperation between Max-Planck-Institute for Limnology, Working group "Tropical Ecology", Plön, West Germany, and Instituto Nacional de Pesquisas da Amazônia, Manaus-Amazonas, Brazil Da cooperaçâo ent¡e Max-Planck-Institut für Limnologie, Arbeitsgruppe Tropenökologie, Plön, Alemanha Oc., e Instituto Nacional de Pesquisas da Amazônia, Manaus-Amazonas, Brasil On the naturâl history and ecology of Meinertellidae (Archaeognatha, I nsecta) from dryland and inundation forests of Central Amazonia by Joachim Adis & Helmut Sturm Dr. Joachim Adis, Max-Planck-Institute for Limnology, Tropical Ecology Working Group, Postfach 165, D -2320Hön, F.R.G. Prof. Dr. Helmut Sturm, Hochschule Hildesheim, Marienburger Platz22, D - 3200 Hildesheim, F.R.G. (accepted for publication: May 1987) Abstract The life-cycle and ecology of four nocturnal species of Meinertellidae aregiven and their adaptation from Amazonian dryland to inundation forests is discussed. In primary and secondary dryland forests, Neomachilellus scandens, N. amazonicus and Meínertellus adisi are arboricolous, show no defined reproduction period andjuveniles are found throughout the year. In inundation forests of the Rio Ncgro valley, which are annually flooded for 5 - 6 months,ly'. scandens, N. adísi and, M. adísi liave one generation per year. Annual inundation is considered as the main reason for the acquisition of a seasonal development. InN. scandens, juveniles hatch from previously submerged eggs on the forest floor at the beginning of the non-inundation period and reach maturity after 3 months. Adults propagate in.the litter, where females deposit their eggs which are subject to the next flooding. Both sexes sub- sequently rnigrate into the trunk/canopy area and perish. -
An Overview of Systematics Studies Concerning the Insect Fauna of British Columbia
J ENTOMOL. Soc. B RIT. COLU MBIA 9 8. DECDmER 200 1 33 An overview of systematics studies concerning the insect fauna of British Columbia ROBERT A. CANNINGS ROYAL BRITISI-I COLUMBIA MUSEUM, 675 BELLEVILLE STREET, VICTORIA, BC, CANADA V8W 9W2 GEOFFREY G.E. SCUDDER DEPARTMENT OF ZOOLOGY, UNIVERSITY OF BRITISI-I COLUMBIA, VANCOUVER, BC, CANADA V6T IZ4 INTRODUCTION This summary of insect systematics pertaining to British Co lumbia is not intended as an hi storical account of entomologists and their work, but rath er is an overview of th e more important studies and publications dealing with the taxonomy, identifi cati on, distribution and faunistics of BC species. Some statistics on th e known size of various taxa are also give n. Many of the systematic references to th e province's insects ca nnot be presented in such a short summary as thi s and , as a res ult, the treatment is hi ghl y se lec tive. It deals large ly with publications appearing after 1950. We examine mainly terrestrial groups. Alth ough Geoff Scudder, Professor of Zoo logy at the University of Briti sh Co lumbi a, at Westwick Lake in the Cariboo, May 1970. Sc udder is a driving force in man y facets of in sect systemat ics in Briti sh Co lum bia and Canada. He is a world authority on th e Hemiptera. Photo: Rob Ca nnin gs. 34 J ENTOMOL. Soc BR IT. COLUMBIA 98, DECEMBER200 1 we mention the aquatic orders (those in which the larv ae live in water but the adults are aerial), they are more fully treated in the companion paper on aquatic in sects in thi s issue (Needham et al.) as are the major aquatic families of otherwise terrestrial orders (e.g. -
Arkansas Endemic Biota: an Update with Additions and Deletions H
Journal of the Arkansas Academy of Science Volume 62 Article 14 2008 Arkansas Endemic Biota: An Update with Additions and Deletions H. Robison Southern Arkansas University, [email protected] C. McAllister C. Carlton Louisiana State University G. Tucker FTN Associates, Ltd. Follow this and additional works at: http://scholarworks.uark.edu/jaas Part of the Botany Commons Recommended Citation Robison, H.; McAllister, C.; Carlton, C.; and Tucker, G. (2008) "Arkansas Endemic Biota: An Update with Additions and Deletions," Journal of the Arkansas Academy of Science: Vol. 62 , Article 14. Available at: http://scholarworks.uark.edu/jaas/vol62/iss1/14 This article is available for use under the Creative Commons license: Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0). Users are able to read, download, copy, print, distribute, search, link to the full texts of these articles, or use them for any other lawful purpose, without asking prior permission from the publisher or the author. This Article is brought to you for free and open access by ScholarWorks@UARK. It has been accepted for inclusion in Journal of the Arkansas Academy of Science by an authorized editor of ScholarWorks@UARK. For more information, please contact [email protected], [email protected]. Journal of the Arkansas Academy of Science, Vol. 62 [2008], Art. 14 The Arkansas Endemic Biota: An Update with Additions and Deletions H. Robison1, C. McAllister2, C. Carlton3, and G. Tucker4 1Department of Biological Sciences, Southern Arkansas University, Magnolia, AR 71754-9354 2RapidWrite, 102 Brown Street, Hot Springs National Park, AR 71913 3Department of Entomology, Louisiana State University, Baton Rouge, LA 70803-1710 4FTN Associates, Ltd., 3 Innwood Circle, Suite 220, Little Rock, AR 72211 1Correspondence: [email protected] Abstract Pringle and Witsell (2005) described this new species of rose-gentian from Saline County glades. -
Description of a New Genus and a New Species of Machilidae (Insecta: Microcoryphia) from Turkey
85 (1) · April 2013 pp. 31–39 Description of a new genus and a new species of Machilidae (Insecta: Microcoryphia) from Turkey Carmen Bach de Roca1,*, Pietro-Paolo Fanciulli2, Francesco Cicconardi2, Rafael Molero- Baltanás3 and Miguel Gaju-Ricart3 1 Department of Animal and Vegetal Biology and Ecology, Autonomous University of Barcelona, 08193 Bellaterra (Barcelona), Spain 2 Dipartimento di Biologia Evolutiva, University of Siena, Via Aldo Moro, 2 - 53100 Siena, Italy 3 Department of Zoology, University of Córdoba, C-1 Campus Rabanales, 14014 Córdoba, Spain * Corresponding author, e-mail: [email protected] Received 20 March 2013 | Accepted 04 April 2013 Published online at www.soil-organisms.de 29 April 2013 | Printed version 30 April 2013 Abstract A new species and a new genus of Microcoryphia from Turkey are described. The new genus, named Turquimachilis has, as its most important distinctive feature, the presence in the male of unique parameres on the IXth urostemite, with proximal protuberances and chaetotaxy. They are different from all the other genera of the order. This alone is sufficient to allow the creation of a new genus. We add other anatomical characteristics that allow us to differentiate the new genus from the closest known genera. The type species is described. Keywords Turquimachilis mendesi | new genus | new species | Charimachilis | Turkey 1. Introduction 2. Material and methods Knowledge of Turkish Microcoryphia is scarce, We received the specimens from the Museum of because since Wygodzinsky (1959) no further work Natural History of Verona. They were collected in 1969 has been published referring to this country. The two (one sample) and 1972 (remaining samples), all of them known families of Microcoryphia are represented conserved in ethanol. -
Pinyon Pine Mortality Alters Communities of Ground-Dwelling Arthropods
Western North American Naturalist 74(2), © 2014, pp. 162–184 PINYON PINE MORTALITY ALTERS COMMUNITIES OF GROUND-DWELLING ARTHROPODS Robert J. Delph1,2,6, Michael J. Clifford2,3, Neil S. Cobb2, Paulette L. Ford4, and Sandra L. Brantley5 ABSTRACT.—We documented the effect of drought-induced mortality of pinyon pine (Pinus edulis Engelm.) on com- munities of ground-dwelling arthropods. Tree mortality alters microhabitats utilized by ground-dwelling arthropods by increasing solar radiation, dead woody debris, and understory vegetation. Our major objectives were to determine (1) whether there were changes in community composition, species richness, and abundance of ground-dwelling arthro- pods associated with pinyon mortality and (2) whether specific habitat characteristics and microhabitats accounted for these changes. We predicted shifts in community composition and increases in arthropod diversity and abundance due to the presumed increased complexity of microhabitats from both standing dead and fallen dead trees. We found signifi- cant differences in arthropod community composition between high and low pinyon mortality environments, despite no differences in arthropod abundance or richness. Overall, 22% (51 taxa) of the arthropod community were identified as being indicators of either high or low mortality. Our study corroborates other research indicating that arthropods are responsive to even moderate disturbance events leading to changes in the environment. These arthropod responses can be explained in part due to the increase in woody debris and reduced canopy cover created by tree mortality. RESUMEN.—Documentamos el efecto de la mortalidad causada por la sequía del pino piñonero (Pinus edulis Engelm.) sobre comunidades de artrópodos subterráneos. Utilizamos tres variantes en el microhábitat de los artrópodos incrementando la radiación solar, desechos de madera muerta y vegetación baja.