Contribution to the Knowledge of Oriental Phasmatodea I: a Taxonomic Study of the Genus Parasinophasma (Phasmatodea: Necrosci
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Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea
Brigham Young University BYU ScholarsArchive Theses and Dissertations 2018-07-01 Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco Brigham Young University Follow this and additional works at: https://scholarsarchive.byu.edu/etd Part of the Life Sciences Commons BYU ScholarsArchive Citation Pacheco, Yelena Marlese, "Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea" (2018). Theses and Dissertations. 7444. https://scholarsarchive.byu.edu/etd/7444 This Thesis is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco A thesis submitted to the faculty of Brigham Young University in partial fulfillment of the requirements for the degree of Master of Science Michael F. Whiting, Chair Sven Bradler Seth M. Bybee Steven D. Leavitt Department of Biology Brigham Young University Copyright © 2018 Yelena Marlese Pacheco All Rights Reserved ABSTRACT Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco Department of Biology, BYU Master of Science Phasmatodea exhibit a variety of cryptic ecomorphs associated with various microhabitats. Multiple ecomorphs are present in the stick insect fauna from Papua New Guinea, including the tree lobster, spiny, and long slender forms. While ecomorphs have long been recognized in phasmids, there has yet to be an attempt to objectively define and study the evolution of these ecomorphs. -
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. -
Changes in Arthropod Abundance and Diversity with Invasive
CHANGES IN ARTHROPOD ABUNDANCE AND DIVERSITY WITH INVASIVE GRASSES A Thesis by ERIN E. CORD Submitted to the College of Graduate Studies Texas A&M University-Kingsville in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August 2011 Major Subject: Range and Wildlife Management CHANGES IN ARTHROPOD ABUNDANCE AND DIVERSITY WITH INVASIVE GRASSES A Thesis by ERIN E. CORD Approved as to style and content by: ______________________________ Andrea R. Litt, Ph.D. (Chairman of Committee) ___________________________ ___________________________ Timothy E. Fulbright, Ph.D. Greta L. Schuster, Ph.D. (Member) (Member) _____________________________ Scott E. Henke, Ph.D. (Chair of Department) _________________________________ Ambrose Anoruo, Ph.D. (Associate VP for Research & Dean, College of Graduate Studies) August 2011 ABSTRACT Changes in Arthropod Abundance and Diversity with Invasive Grasses (August 2011) Erin E. Cord, B.S., University Of Delaware Chairman of Committee: Dr. Andrea R. Litt Invasive grasses can alter plant communities and can potentially affect arthropods due to specialized relationships with certain plants as food resources and reproduction sites. Kleberg bluestem (Dichanthium annulatum) is a non-native grass and tanglehead (Heteropogon contortus) is native to the United States, but recently has become dominant in south Texas. I sought to: 1) quantify changes in plant and arthropod communities in invasive grasses compared to native grasses, and 2) determine if grass origin would alter effects. I sampled vegetation and arthropods on 90 grass patches in July and September 2009 and 2010 on the King Ranch in southern Texas. Arthropod communities in invasive grasses were less diverse and abundant, compared to native grasses; I also documented differences in presence and abundance of certain orders and families. -
Insects for Human Consumption
Chapter 18 Insects for Human Consumption Marianne Shockley1 and Aaron T. Dossey2 1Department of Entomology, University of Georgia, Athens, GA, USA, 2All Things Bugs, Gainesville, FL, USA 18.1. INTRODUCTION The utilization of insects as a sustainable and secure source of animal-based food for the human diet has continued to increase in popularity in recent years (Ash et al., 2010; Crabbe, 2012; Dossey, 2013; Dzamba, 2010; FAO, 2008; Gahukar, 2011; Katayama et al., 2008; Nonaka, 2009; Premalatha et al., 2011; Ramos- Elorduy, 2009; Smith, 2012; Srivastava et al., 2009; van Huis, 2013; van Huis et al., 2013; Vantomme et al., 2012; Vogel, 2010; Yen, 2009a, b). Throughout the world, a large portion of the human population consumes insects as a regular part of their diet (Fig. 18.1). Thousands of edible species have been identified (Bukkens, 1997; Bukkens and Paoletti, 2005; DeFoliart, 1999; Ramos-Elorduy, 2009). However, in regions of the world where Western cultures dominate, such as North America and Europe, and in developing countries heavily influenced by Western culture, mass media have negatively influenced the public’s percep- tion of insects by creating or reinforcing fears and phobias (Kellert, 1993; Looy and Wood, 2006). Nonetheless, the potentially substantial benefits of farming and utilizing insects as a primary dietary component, particularly to supplement or replace foods and food ingredients made from vertebrate livestock, are gain- ing increased attention even in Europe and the United States. Thus, we present this chapter to -
Phasmida (Stick and Leaf Insects)
● Phasmida (Stick and leaf insects) Class Insecta Order Phasmida Number of families 8 Photo: A leaf insect (Phyllium bioculatum) in Japan. (Photo by ©Ron Austing/Photo Researchers, Inc. Reproduced by permission.) Evolution and systematics Anareolatae. The Timematodea has only one family, the The oldest fossil specimens of Phasmida date to the Tri- Timematidae (1 genus, 21 species). These small stick insects assic period—as long ago as 225 million years. Relatively few are not typical phasmids, having the ability to jump, unlike fossil species have been found, and they include doubtful almost all other species in the order. It is questionable whether records. Occasionally a puzzle to entomologists, the Phasmida they are indeed phasmids, and phylogenetic research is not (whose name derives from a Greek word meaning “appari- conclusive. Studies relating to phylogeny are scarce and lim- tion”) comprise stick and leaf insects, generally accepted as ited in scope. The eggs of each phasmid are distinctive and orthopteroid insects. Other alternatives have been proposed, are important in classification of these insects. however. There are about 3,000 species of phasmids, although in this understudied order this number probably includes about 30% as yet unidentified synonyms (repeated descrip- Physical characteristics tions). Numerous species still await formal description. Stick insects range in length from Timema cristinae at 0.46 in (11.6 mm) to Phobaeticus kirbyi at 12.9 in (328 mm), or 21.5 Extant species usually are divided into eight families, in (546 mm) with legs outstretched. Numerous phasmid “gi- though some researchers cite just two, based on a reluctance ants” easily rank as the world’s longest insects. -
(Walking Leaves) (Insecta, Orthoptera) 129-141 ©Zoologische Staatssammlung München;Download
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Spixiana, Zeitschrift für Zoologie Jahr/Year: 2003 Band/Volume: 026 Autor(en)/Author(s): Zompro Oliver, Größer Detlef Artikel/Article: A generic revision of the insect order Phasmatodea: The genera of the areolate stick insect family Phylliidae (Walking Leaves) (Insecta, Orthoptera) 129-141 ©Zoologische Staatssammlung München;download: http://www.biodiversitylibrary.org/; www.biologiezentrum.at -> SPIXIANA 26 129-141 München, Ol. Juli 2003 ISSN 0341-8391 A generic revision of the insect order Phasmatodea: The genera of the areolate stick insect family Phylliidae (Walking Leaves) (Insecta, Orthoptera) Oliver Zompro & Detlef Größer Zompro, O. & D. Größer (2003): A generic revision of the insect order Phasma- todea: The genera of the areolate stick insect family Phviliidae (Walking Leaves) (Insecta: Orthoptera). - Spixiana 26/2: 129-141 The genera of the family Phylliidae (Walking Leaves) (Phasmatodea: Areoiatae) are revised and the relationships between them discussed. Nniiopln/Uiuin Redten- bacher, 1906 differs strikingly from the other genera and is transferred in the Nanophylliini, trib. nov. A key to genera and species is provided. Nniiopliylliiim adisi, spec. nov. from New Guinea is described for the first time. The paper includes a key to the species of Nmwpln/Uiiiin. Dr. Oliver Zompro, Max-Planck-Institut für Limnologie, Arbeitsgruppe Tro- penökologie, August-ThienemamvStraße 2, D-24306 Plön, Germany; e-mail: [email protected]; Website: www.sungaya.de Detlef Größer, Ernst-Lemmer-Ring 119, D-14165 Berlin, Germany; e-mail: [email protected]; Website: www.Phvllium.de Introduction Material and methods The species of the areolate family Phylliidae are Material in various public and private collections was well known as "Walking Leaves" or "Leaf Insects". -
Phasmatodea PHASMATODEA
Phasmatodea PHASMATODEA Walkingsticks / Stick Insects / Leaf Insects / Phasmids The name Phasmatodea, derived from the Greek "phasm" meaning phantom, refers to the cryptic appearance and behavior of these insects. Classification Life History & Ecology Distribution Physical Features Economic Importance Major Families Fact File Hot Links Life History & Ecology: The leaf and stick insects are sometimes grouped as a family or suborder of Orthoptera. All species are herbivores. As the name "walkingstick" implies, most phasmids are slender, cylindrical, and cryptically colored to resemble the twigs and branches on which they live. Members of the family Timemidae (=Phyllidae) bear a strong resemblance to leaves: abdomens are broad and flat, legs have large lateral extensions, and coloration is primarily brown, green, or yellow. Most walkingsticks are slow-moving insects, a behavior pattern that is consistent with their cryptic lifestyle. In a few tropical species, the adults have well-developed wings, but most phasmids are brachypterous (reduced wings) or secondarily wingless. Stick insects are most abundant in the tropics where some http://www.cals.ncsu.edu/course/ent425/compendium/stick.html (1 of 5) [10/24/2007 12:05:29 PM] Phasmatodea species may be up to 30 cm (12 inches) in length. Females do not have a well- developed ovipositor so they cannot insert their eggs into host plant tissue like most other Orthoptera. Instead, the eggs are dropped singly onto the ground, sometimes from great heights. Distribution: Common in tropical and subtropical climates where they are found living on their host plants. North Worldwide America Number of Families 2 3 Number of Species 32 >2500 Classification: Hemimetabola incomplete development (egg, nymph, adult) Orthopteroid closely related to Orthoptera and Dermaptera Physical Features: Adults and Immatures http://www.cals.ncsu.edu/course/ent425/compendium/stick.html (2 of 5) [10/24/2007 12:05:29 PM] Phasmatodea 1. -
SYNAPOMORPHIES ORTHOPTERA, Sensu Stricto Grasshoppers
The Orthopteridan Orders Orthoptera Phasmatodea Plecoptera PLECOPTERIDA Embioptera Zoraptera Dermaptera POLYORTHOPTERA Grylloblattodea Mantophasmatodea Phasmatodea ORTHOPTERIDA Orthoptera Blattodea Perhaps similar Isoptera development of the gonoplac over 2nd DICTYOPTERA valvulae Mantodea Plecoptera PLECOPTERIDA Embioptera Zoraptera Dermaptera Grylloblattodea Mantophasmatodea Phasmatodea ORTHOPTERIDA Orthoptera • Second valvula reduced, with developmentBlattodea of gonoplac as functional ovipositor • Enlarged precostal field in forewingIsoptera DICTYOPTERA Mantodea ORTHOPTERA, sensu stricto Grasshoppers, Locusts, Katydids, Crickets, Wetas What is a “Weta”? A giant cricket! New Zealand Maori name of wetapunga that was given to the giant weta. Wetapunga translates roughly to "God of ugly things.” Wetas and king crickets occur principally in New Zealand and Australia. Can reach 90 mm (3.5 in) and 70 grams (2.5 oz). Orthoptera Ensifera Stenopelmatoidea Anostostomatidae ORTHOPTERA, sensu stricto Grasshoppers, Locusts, Katydids, Crickets, Wetas SYNAPOMORPHIES • Lateral flange of pronotum largely covering pleuron, which • Hind leg modified for jumping correspondingly becomes by straightening of femoral/tibial desclerotized joint (cryptopleuron) • Femur enlarged to • Hind tibia with 2 dorsal accommodate large tibia rows of teeth extensor muscle ORTHOPTERA, sensu stricto Grasshoppers, Locusts, Katydids, Crickets, Wetas SYNAPOMORPHIES • First thoracic spiracle horizontally divided • Wings inclined over abdomen at rest • Wing pads of late nymphal -
Preliminary Checklist of the Orthopteroid Insects (Blattodea, Mantodea, Phasmatodea,Orthoptera) of Texas
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida March 2001 Preliminary checklist of the orthopteroid insects (Blattodea, Mantodea, Phasmatodea,Orthoptera) of Texas John A. Stidham Garland, TX Thomas A. Stidham University of California, Berkeley, CA Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Stidham, John A. and Stidham, Thomas A., "Preliminary checklist of the orthopteroid insects (Blattodea, Mantodea, Phasmatodea,Orthoptera) of Texas" (2001). Insecta Mundi. 180. https://digitalcommons.unl.edu/insectamundi/180 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI, Vol. 15, No. 1, March, 2001 35 Preliminary checklist of the orthopteroid insects (Blattodea, Mantodea, Phasmatodea,Orthoptera) of Texas John A. Stidham 301 Pebble Creek Dr., Garland, TX 75040 and Thomas A. Stidham Department of Integrative Biology, Museum of Paleontology, and Museum of Vertebrate Zoology, University of California, Berkeley, CA 94720, Abstract: Texas has one of the most diverse orthopteroid assemblages of any state in the United States, reflecting the varied habitats found in the state. Three hundred and eighty-nine species and 78 subspecies of orthopteroid insects (Blattodea, Mantodea, Phasmatodea, and Orthoptera) have published records for the state of Texas. This is the first such comprehensive checklist for Texas and should aid future work on these groups in this area. Introduction (Flook and Rowell, 1997). -
Classification: Phamatodea
NOMINA INSECTA NEARCTICA 637 CLASSIFICATION The primary data comes from unpublished database files of the author. The classification is based on: Bradley, J.D., and B.S. Galil. 1977. The taxonomic arrangement of the Phasmatodea with keys to the subfamilies and tribes. Proceedings of the Entomological Society of Washington, 79:176-208. HETERONEMIIDAE Heteronemiinae: Diapheromera, Manomera, Megaphasma, Pseudosermyle, Sermyle. Pachymorphinae: Parabacillus. PHASMATIDAE Cladomorphinae: Aplopus. TIMEMATIDAE Timema. PSEUDOPHASMATIDAE Pseudophasmatinae: Anisomorpha. Family # Names # Valid Heteronemiidae 29 20 Phasmatidae 1 1 Pseudophasmatidae 5 2 Timematidae 10 10 Total 45 33 PHASMATODEA 638 NOMINA INSECTA NEARCTICA HETERONEMIIDAE Anisomorpha Gray 1835 Anisomorpha buprestoides Stoll 1813 (Phasma) Diapheromera Gray 1835 Phasma vermicularis Stoll 1813 Syn. Spectrum bivittatum Say 1828 Syn. Diapheromera arizonensis Caudell 1903 (Diapheromera) Phasma calamus Burmeister 1838 Syn. Diapheromera carolina Scudder 1901 (Diapheromera) Anisomorpha ferruginea Beauvois 1805 (Phasma) Diapheromera covilleae Rehn and Hebard 1909 (Diapheromera) Diapheromera femoratum Say 1824 (Spectrum) Diapheromera sayi Gray 1835 Syn. Bacunculus laevissimus Brunner 1907 Syn. Diapheromera persimilis Caudell 1904 (Diapheromera) TIMEMATIDAE Bacunculus texanus Brunner 1907 Syn. Diapheromera dolichocephala Brunner 1907 Syn. Diapheromera tamaulipensis Rehn 1909 (Diapheromera) Diapheromera torquata Hebard 1934 (Diapheromera) Timema Scudder 1895 Diapheromera velii Walsh 1864 (Diapheromera) -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Phasma Gigas from New Ireland Mark Bushell
ISSN 0966-0011 PHASMID STUDIES. volume 8, numbers 1 & 2. December 1999. Editor: P.E. Bragg. Published by the Phasmid Study Group. Phasmid Studies ISSN 0966-0011 volume 8, numbers 1 & 2. Contents Studies of the genus Phalces Stal Paul D. Brock . 1 Redescription of Mantis filiformes Fabricius (Phasmatidae: Bacteriinae) Paul D. Brock . 9 Phasmida in Oceania Allan Harman . 13 A Report on a Culture of Phasma gigas from New Ireland Mark Bushell . 20 Reviews and Abstracts Phasmid Abstracts 25 Cover illustration: Female Spinodares jenningsi Bragg, drawing by P.E. Bragg. Studies of the genus Phalces Stal Paul D. Brock, "Papillon", 40 Thorndike Road, Slough SU ISR, UK. Abstract Phalces tuberculatus sp.n. is described from Eland's Bay, Cape Province, South Africa. A key is given to distinguish the Phalces species. Brief notes are given on behaviour, foodplants, and culture notes in the case of P. longiscaphus (de Haan). Key words: Phasmida, Phalces, Phalcestuberculatus sp.n, Introduction As part of my studies on South African stick-insects, I visited Cape Town in September 1998. My research included an examination of the entomology collection at the South African Museum in Cape Town, in addition to material of Phalces species in various museums, observing P. longiscaphus in the wild and rearing this species in captivity. The observations include the description of Phalces tuberculatus sp.n. and a key to distinguish the three Phalces species (of which a Madagascan insect is unlikely to belong to this genus). Museum codens are given below: BMNH Natural History Museum, London, U.K. NHMW Naturhistorisches Museum, Wien, Austria.