Fossil Insects from the Tertiary Sediments at Dinmore, Queensland
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The Wing Venation of Odonata
International Journal of Odonatology, 2019 Vol. 22, No. 1, 73–88, https://doi.org/10.1080/13887890.2019.1570876 The wing venation of Odonata John W. H. Trueman∗ and Richard J. Rowe Research School of Biology, Australian National University, Canberra, Australia (Received 28 July 2018; accepted 14 January 2019) Existing nomenclatures for the venation of the odonate wing are inconsistent and inaccurate. We offer a new scheme, based on the evolution and ontogeny of the insect wing and on the physical structure of wing veins, in which the veins of dragonflies and damselflies are fully reconciled with those of the other winged orders. Our starting point is the body of evidence that the insect pleuron and sternum are foreshortened leg segments and that wings evolved from leg appendages. We find that all expected longitudinal veins are present. The costa is a short vein, extending only to the nodus, and the entire costal field is sclerotised. The so-called double radial stem of Odonatoidea is a triple vein comprising the radial stem, the medial stem and the anterior cubitus, the radial and medial fields from the base of the wing to the arculus having closed when the basal sclerites fused to form a single axillary plate. In the distal part of the wing the medial and cubital fields are secondarily expanded. In Anisoptera the remnant anal field also is expanded. The dense crossvenation of Odonata, interpreted by some as an archedictyon, is secondary venation to support these expanded fields. The evolution of the odonate wing from the palaeopteran ancestor – first to the odonatoid condition, from there to the zygopteran wing in which a paddle-shaped blade is worked by two strong levers, and from there through grade Anisozygoptera to the anisopteran condition – can be simply explained. -
A Synopsis of Baltic Amber Termites (Isoptera)
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/237506136 A synopsis of Baltic amber termites (Isoptera) Article · January 2007 CITATIONS READS 14 49 3 authors, including: David Grimaldi American Museum of Natural History 250 PUBLICATIONS 4,765 CITATIONS SEE PROFILE All content following this page was uploaded by David Grimaldi on 17 July 2015. The user has requested enhancement of the downloaded file. All in-text references underlined in blue are added to the original document and are linked to publications on ResearchGate, letting you access and read them immediately. Stuttgarter Beiträge zur Naturkunde Serie B (Geologie und Paläontologie) Herausgeber: Staatliches Museum für Naturkunde, Rosenstein 1, D-70191 Stuttgart Stuttgarter Beitr. Naturk. Ser. B Nr. 372 20 S., 10 Abb. Stuttgart, 28. 12. 2007 A synopsis of Baltic amber termites (Isoptera) MICHAEL S. ENGEL, DAVID A. GRIMALDI & KUMAR KRISHNA Abstract A brief overview and dichotomous key is provided for those termites (Isoptera) occurring in middle Eocene (Lutetian) Baltic amber. Ten species in seven genera are presently docu- mented from Baltic amber, these being as follows: Garmitermes succineus n. gen. n. sp., Ter- mopsis bremii (HEER), T. ukapirmasi n. sp., Archotermopsis tornquisti ROSEN, Proelectroter- mes berendtii (PICTET-BARABAN), Electrotermes affinis (HAGEN), E. girardi (GIEBEL), Reti- culitermes antiquus (GERMAR), R. minimus SNYDER, and Parastylotermes robustus (ROSEN). Garmitermes succineus n. gen. n. sp. is the first Mastotermes-like termite discovered in Baltic amber. Hemerobites GERMAR, a senior synonym of Reticulitermes HOLMGREN, is designated as a nomen oblitum under the ICZN rules. Maresa GIEBEL, another senior synonym of Reti- culitermes, is tentatively suppressed pending a petition to the ICZN to preserve the latter name. -
Cómo Citar El Artículo Número Completo Más Información Del
Acta zoológica mexicana ISSN: 0065-1737 ISSN: 2448-8445 Instituto de Ecología A.C. García, Mauricio; Camacho, Jesús; Dorado, Idelma Dos nuevas especies de Termitaradus Myers, 1924 (Hemiptera: Termitaphididae), de Venezuela y observaciones sobre la familia Acta zoológica mexicana, vol. 32, núm. 3, 2016, pp. 348-358 Instituto de Ecología A.C. Disponible en: http://www.redalyc.org/articulo.oa?id=57549165012 Cómo citar el artículo Número completo Sistema de Información Científica Redalyc Más información del artículo Red de Revistas Científicas de América Latina y el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto ISSN 0065-1737 (NUEVA SERIE) 32(3) 2016 DOS NUEVAS ESPECIES DE TERMITARADUS MYERS, 1924 (HEMIPTERA: TERMITAPHIDIDAE), DE VENEZUELA Y OBSERVACIONES SOBRE LA FAMILIA TWO NEW SPECIES OF TERMITARADUS MYERS, 1924 (HEMIPTERA: TERMITAPHIDIDAE) OF VENEZUELA, AND OBSERVATIONS ON THE FAMILY Mauricio GARCÍA,¹ Jesús CAMACHO² e Idelma DORADO² ¹ Centro de Investigaciones Biológicas (CIB), Facultad de Humanidades y Educación, Edificio de Postgrado, Universidad del Zulia, Apdo. 526, A-4001, Venezuela. ² Museo de Artrópodos de la Universidad del Zulia (MALUZ). Departamento Fitosanitario, Facultad de Agronomía, Universidad del Zulia, Apdo. 526, Maracaibo A-4001, Zulia, Venezuela. <[email protected]>; <[email protected]>; <[email protected]> Recibido: 28/03/2016; aceptado: 30/08/2016 Editor asociado responsable: Alfonso Neri García Aldrete García, M., Camacho, J. & Dorado, I. (2016). Dos nuevas especies García, M., Camacho, J. & Dorado, I. (2016). Two new species of de Termitaradus Myers, 1924 (Hemiptera: Termitaphididae), de Termitaradus Myers, 1924 (Hemiptera: Termitaphididae) of Ven- Venezuela y observaciones sobre la familia. -
Evaluation of the Chemical Defense Fluids of Macrotermes Carbonarius
www.nature.com/scientificreports OPEN Evaluation of the chemical defense fuids of Macrotermes carbonarius and Globitermes sulphureus as possible household repellents and insecticides S. Appalasamy1,2*, M. H. Alia Diyana2, N. Arumugam2 & J. G. Boon3 The use of chemical insecticides has had many adverse efects. This study reports a novel perspective on the application of insect-based compounds to repel and eradicate other insects in a controlled environment. In this work, defense fuid was shown to be a repellent and insecticide against termites and cockroaches and was analyzed using gas chromatography-mass spectrometry (GC– MS). Globitermes sulphureus extract at 20 mg/ml showed the highest repellency for seven days against Macrotermes gilvus and for thirty days against Periplaneta americana. In terms of toxicity, G. sulphureus extract had a low LC50 compared to M. carbonarius extract against M. gilvus. Gas chromatography–mass spectrometry analysis of the M. carbonarius extract indicated the presence of six insecticidal and two repellent compounds in the extract, whereas the G. sulphureus extract contained fve insecticidal and three repellent compounds. The most obvious fnding was that G. sulphureus defense fuid had higher potential as a natural repellent and termiticide than the M. carbonarius extract. Both defense fuids can play a role as alternatives in the search for new, sustainable, natural repellents and termiticides. Our results demonstrate the potential use of termite defense fuid for pest management, providing repellent and insecticidal activities comparable to those of other green repellent and termiticidal commercial products. A termite infestation could be silent, but termites are known as destructive urban pests that cause structural damage by infesting wooden and timber structures, leading to economic loss. -
Blattodea: Hodotermitidae) and Its Role As a Bioindicator of Heavy Metal Accumulation Risks in Saudi Arabia
Article Characterization of the 12S rRNA Gene Sequences of the Harvester Termite Anacanthotermes ochraceus (Blattodea: Hodotermitidae) and Its Role as A Bioindicator of Heavy Metal Accumulation Risks in Saudi Arabia Reem Alajmi 1,*, Rewaida Abdel-Gaber 1,2,* and Noura AlOtaibi 3 1 Zoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia 2 Zoology Department, Faculty of Science, Cairo University, Cairo 12613, Egypt 3 Department of Biology, Faculty of Science, Taif University, Taif 21974, Saudi Arabia; [email protected] * Correspondence: [email protected] (R.A.), [email protected] (R.A.-G.) Received: 28 December 2018; Accepted: 3 February 2019; Published: 8 February 2019 Abstract: Termites are social insects of economic importance that have a worldwide distribution. Identifying termite species has traditionally relied on morphometric characters. Recently, several mitochondrial genes have been used as genetic markers to determine the correlation between different species. Heavy metal accumulation causes serious health problems in humans and animals. Being involved in the food chain, insects are used as bioindicators of heavy metals. In the present study, 100 termite individuals of Anacanthotermes ochraceus were collected from two Saudi Arabian localities with different geoclimatic conditions (Riyadh and Taif). These individuals were subjected to morphological identification followed by molecular analysis using mitochondrial 12S rRNA gene sequence, thus confirming the morphological identification of A. ochraceus. Furthermore, a phylogenetic analysis was conducted to determine the genetic relationship between the acquired species and other termite species with sequences previously submitted in the GenBank database. Several heavy metals including Ca, Al, Mg, Zn, Fe, Cu, Mn, Ba, Cr, Co, Be, Ni, V, Pb, Cd, and Mo were measured in both collected termites and soil samples from both study sites. -
Phylogeny of Ensifera (Hexapoda: Orthoptera) Using Three Ribosomal Loci, with Implications for the Evolution of Acoustic Communication
Molecular Phylogenetics and Evolution 38 (2006) 510–530 www.elsevier.com/locate/ympev Phylogeny of Ensifera (Hexapoda: Orthoptera) using three ribosomal loci, with implications for the evolution of acoustic communication M.C. Jost a,*, K.L. Shaw b a Department of Organismic and Evolutionary Biology, Harvard University, USA b Department of Biology, University of Maryland, College Park, MD, USA Received 9 May 2005; revised 27 September 2005; accepted 4 October 2005 Available online 16 November 2005 Abstract Representatives of the Orthopteran suborder Ensifera (crickets, katydids, and related insects) are well known for acoustic signals pro- duced in the contexts of courtship and mate recognition. We present a phylogenetic estimate of Ensifera for a sample of 51 taxonomically diverse exemplars, using sequences from 18S, 28S, and 16S rRNA. The results support a monophyletic Ensifera, monophyly of most ensiferan families, and the superfamily Gryllacridoidea which would include Stenopelmatidae, Anostostomatidae, Gryllacrididae, and Lezina. Schizodactylidae was recovered as the sister lineage to Grylloidea, and both Rhaphidophoridae and Tettigoniidae were found to be more closely related to Grylloidea than has been suggested by prior studies. The ambidextrously stridulating haglid Cyphoderris was found to be basal (or sister) to a clade that contains both Grylloidea and Tettigoniidae. Tree comparison tests with the concatenated molecular data found our phylogeny to be significantly better at explaining our data than three recent phylogenetic hypotheses based on morphological characters. A high degree of conflict exists between the molecular and morphological data, possibly indicating that much homoplasy is present in Ensifera, particularly in acoustic structures. In contrast to prior evolutionary hypotheses based on most parsi- monious ancestral state reconstructions, we propose that tegminal stridulation and tibial tympana are ancestral to Ensifera and were lost multiple times, especially within the Gryllidae. -
A Giant Termite from the Late Miocene of Styria, Austria (Isoptera)
Naturwissenschaften DOI 10.1007/s00114-008-0480-y ORIGINAL PAPER A giant termite from the Late Miocene of Styria, Austria (Isoptera) Michael S. Engel & Martin Gross Received: 9 September 2008 /Revised: 11 November 2008 /Accepted: 13 November 2008 # Springer-Verlag 2008 Abstract A giant termite is described and figured from the and ants with 19,254 and 12,463 species, respectively: Late Miocene of the Styrian Basin in southeastern Austria. numbers valid as of 7 November 2008), without the vital Gyatermes styriensis gen. n. et sp. n. is represented by a role of termites, entire ecosystems would crash (Grimaldi relatively complete forewing, with basal scale. The fossil and Engel 2005). Like honeybees, ants, some wasps, and a approximates in size the largest of all termites today and is few other organisms, all termites are advanced eusocial, the largest fossil termite on record. The presence of this with individuals behaviorally and anatomically specialized species in the Late Miocene fauna of Europe indicates that for specific tasks within the colony. This organization climatic conditions were appropriate for the persistence of accounts for the efficiency with which termites process the species and colonies requiring relatively stable, warm most abundant terrestrial biomolecule, lignocellulose, and conditions. The genus is primitive in overall features but for the billions of dollars of damage colonies impose on shares some similarity with the dampwood termites. human architectural structures. For good or bad, the termites are a dominant force in the world, impacting both Keywords Insecta . Isoptera . Termites . Miocene . Tertiary . natural and human-created ecosystems. Yet, the history that Austria shaped this force has historically been obscured or ignored (Grimaldi and Engel 2005). -
Insect Morphology and Systematics (Ento-131) - Notes
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/276175248 Insect Morphology and Systematics (Ento-131) - Notes Book · April 2010 CITATIONS READS 0 14,110 1 author: Cherukuri Sreenivasa Rao National Institute of Plant Health Management (NIPHM), Hyderabad, India 36 PUBLICATIONS 22 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Agricultural College, Jagtial View project ICAR-All India Network Project on Pesticide Residues View project All content following this page was uploaded by Cherukuri Sreenivasa Rao on 12 May 2015. The user has requested enhancement of the downloaded file. Insect Morphology and Systematics ENTO-131 (2+1) Revised Syllabus Dr. Cherukuri Sreenivasa Rao Associate Professor & Head, Department of Entomology, Agricultural College, JAGTIAL EntoEnto----131131131131 Insect Morphology & Systematics Prepared by Dr. Cherukuri Sreenivasa Rao M.Sc.(Ag.), Ph.D.(IARI) Associate Professor & Head Department of Entomology Agricultural College Jagtial-505529 Karminagar District 1 Page 2010 Insect Morphology and Systematics ENTO-131 (2+1) Revised Syllabus Dr. Cherukuri Sreenivasa Rao Associate Professor & Head, Department of Entomology, Agricultural College, JAGTIAL ENTO 131 INSECT MORPHOLOGY AND SYSTEMATICS Total Number of Theory Classes : 32 (32 Hours) Total Number of Practical Classes : 16 (40 Hours) Plan of course outline: Course Number : ENTO-131 Course Title : Insect Morphology and Systematics Credit Hours : 3(2+1) (Theory+Practicals) Course In-Charge : Dr. Cherukuri Sreenivasa Rao Associate Professor & Head Department of Entomology Agricultural College, JAGTIAL-505529 Karimanagar District, Andhra Pradesh Academic level of learners at entry : 10+2 Standard (Intermediate Level) Academic Calendar in which course offered : I Year B.Sc.(Ag.), I Semester Course Objectives: Theory: By the end of the course, the students will be able to understand the morphology of the insects, and taxonomic characters of important insects. -
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. -
Methane Production in Terrestrial Arthropods (Methanogens/Symbiouis/Anaerobic Protsts/Evolution/Atmospheric Methane) JOHANNES H
Proc. Nati. Acad. Sci. USA Vol. 91, pp. 5441-5445, June 1994 Microbiology Methane production in terrestrial arthropods (methanogens/symbiouis/anaerobic protsts/evolution/atmospheric methane) JOHANNES H. P. HACKSTEIN AND CLAUDIUS K. STUMM Department of Microbiology and Evolutionary Biology, Faculty of Science, Catholic University of Nijmegen, Toernooiveld, NL-6525 ED Nimegen, The Netherlands Communicated by Lynn Margulis, February 1, 1994 (receivedfor review June 22, 1993) ABSTRACT We have screened more than 110 represen- stoppers. For 2-12 hr the arthropods (0.5-50 g fresh weight, tatives of the different taxa of terrsrial arthropods for depending on size and availability of specimens) were incu- methane production in order to obtain additional information bated at room temperature (210C). The detection limit for about the origins of biogenic methane. Methanogenic bacteria methane was in the nmol range, guaranteeing that any occur in the hindguts of nearly all tropical representatives significant methane emission could be detected by gas chro- of millipedes (Diplopoda), cockroaches (Blattaria), termites matography ofgas samples taken at the end ofthe incubation (Isoptera), and scarab beetles (Scarabaeidae), while such meth- period. Under these conditions, all methane-emitting species anogens are absent from 66 other arthropod species investi- produced >100 nmol of methane during the incubation pe- gated. Three types of symbiosis were found: in the first type, riod. All nonproducers failed to produce methane concen- the arthropod's hindgut is colonized by free methanogenic trations higher than the background level (maximum, 10-20 bacteria; in the second type, methanogens are closely associated nmol), even if the incubation time was prolonged and higher with chitinous structures formed by the host's hindgut; the numbers of arthropods were incubated. -
Fossil Calibrations for the Arthropod Tree of Life
bioRxiv preprint doi: https://doi.org/10.1101/044859; this version posted June 10, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. FOSSIL CALIBRATIONS FOR THE ARTHROPOD TREE OF LIFE AUTHORS Joanna M. Wolfe1*, Allison C. Daley2,3, David A. Legg3, Gregory D. Edgecombe4 1 Department of Earth, Atmospheric & Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA 2 Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK 3 Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PZ, UK 4 Department of Earth Sciences, The Natural History Museum, Cromwell Road, London SW7 5BD, UK *Corresponding author: [email protected] ABSTRACT Fossil age data and molecular sequences are increasingly combined to establish a timescale for the Tree of Life. Arthropods, as the most species-rich and morphologically disparate animal phylum, have received substantial attention, particularly with regard to questions such as the timing of habitat shifts (e.g. terrestrialisation), genome evolution (e.g. gene family duplication and functional evolution), origins of novel characters and behaviours (e.g. wings and flight, venom, silk), biogeography, rate of diversification (e.g. Cambrian explosion, insect coevolution with angiosperms, evolution of crab body plans), and the evolution of arthropod microbiomes. We present herein a series of rigorously vetted calibration fossils for arthropod evolutionary history, taking into account recently published guidelines for best practice in fossil calibration. -
Dermaptera Hindwing Structure and Folding: New Evidence for Familial, Ordinal and Superordinal Relationships Within Neoptera (Insecta)
Eur. J. Entorno!. 98: 445-509, 2001 ISSN 1210-5759 Dermaptera hindwing structure and folding: New evidence for familial, ordinal and superordinal relationships within Neoptera (Insecta) Fabian HAAS1 and Jarmila KUKALOVÂ-PECK2 1 Section ofBiosystematic Documentation, University ofUlm, Helmholtzstr. 20, D-89081 Ulm, Germany; e-mail: [email protected] 2Department ofEarth Sciences, Carleton University, Ottawa, ON K1S 5B6, Canada; e-mail: [email protected] Key words.Dermaptera, higher phylogenetics, Pterygota, insect wings, wing folding, wing articulation, protowing Abstract. The Dermaptera are a small order of insects, marked by reduced forewings, hindwings with a unique and complicated folding pattern, and by pincer-like cerci. Hindwing characters of 25 extant dermapteran species are documented. The highly derived hindwing venation and articulation is accurately homologized with the other pterygote orders for the first time. The hindwing base of Dermaptera contains phylogenetically informative characters. They are compared with their homologues in fossil dermapteran ancestors, and in Plecoptera, Orthoptera (Caelifera), Dictyoptera (Mantodea, Blattodea, Isoptera), Fulgoromorpha and Megaloptera. A fully homologized character matrix of the pterygote wing complex is offered for the first time. The wing venation of the Coleo- ptera is re-interpreted and slightly modified . The all-pterygote character analysis suggests the following relationships: Pterygota: Palaeoptera + Neoptera; Neoptera: [Pleconeoptera + Orthoneoptera] +