Arthropoda: Characters and Classifications | Invertebrate Zoology Article Shared By

Total Page:16

File Type:pdf, Size:1020Kb

Arthropoda: Characters and Classifications | Invertebrate Zoology Article Shared By Navigation Arthropoda: Characters and Classifications | Invertebrate Zoology Article Shared by ADVERTISEMENTS: In this article we will discuss about Arthropoda:- 1. General Characters of Arthropoda 2. Classification of Arthropoda. General Characters of Arthropoda: 1. Arthropods are triploblastic, bilaterally symmetrical, metamerically segmented animals. 2. Body of Arthropoda is covered with a thick chitinous cuticle forming an exoskeleton. ADVERTISEMENTS: 3. Body segments usually bear paired lateral and jointed appendages. 4. Musculature is not continuous but comprises separate striped muscles. 5. Body cavity is haemocoel. The true coelom is reduced to the spaces of the genital and excretory organs. 6. Digestive tract is complete, mouth and anus lie at opposite ends of the body. ADVERTISEMENTS: 7. Circulatory system is open with dorsal heart and arteries but without capillaries. 8. Respiration through general body surface, by gills in aquatic forms, tracheae or book lungs in terrestrial forms. 9. True nephridia are absent; excretion by coelomoducts or Malpighian tubules or green or coxal glands. 10. Cilia are entirely absent from all parts of the body. 11. Sexes are generally separate and sexual dimorphism is often exhibited by several forms. 12. Fertilisation is internal. Development is usually indirect through larval stages. 13. Parental care is also often well marked in many arthropods. 14. Most diversified group inhabiting the land, water and air. Classification of Arthropoda: Phylum Arthropoda and its various groups have been classified differently by different workers. But the classification of Arthropoda followed in the present text is generally based on Vandel (1949), Snodgrass (1960) and Storer (1979). ADVERTISEMENTS: Onychophora, however, was considered to be arthropod for a long time but the modern trend is to consider it as an independent group of segmented animals. Subphylum I. Trilobitomorpha: (Gr., tria = three + lobos = lobe + morphe – form): 1. Represented by fossil trilobites only. 2. Body separated by two longitudinal furrows into three lobes. ADVERTISEMENTS: 3. Except the last segment all segments bear biramous appendages. 4. All were marine forms. 5. All were bottom dwellers, i.e., benthozoic and existed from Cambrian to Permian. Examples: ADVERTISEMENTS: Triarthrus, Dalmanites. Subphylum II. Chelicerata: (Gr., chele = claw + keros = horn + ata = group): 1. Body divisible into cephalothorax or prosoma and abdomen or opisthosoma. 2. First pair of appendages are chelicerae which are preoral and feeding in function. ADVERTISEMENTS: 3. Second pair of appendages are pedipalpi which are postoral. 4. Antennae and true jaws not found. 5. Mostly terrestrial and predaceous. Class 1. Merostomata: 1. Exclusively aquatic, all marine. 2. Prosoma bears compound eyes placed laterally; it is broadly jointed to abdomen. 3. Five or six pairs of appendages in abdomen modified as gills or branchiae for respiration. 4. Abdomen ends in a spike-like long telson. Subclass I. Xiphosura: 1. Prosoma is convex covered by a broad horse-shoe-shaped carapace. 2. Prosoma bears six pairs of appendages. 3. Opisthosoma hexagonal consisting of six mesosomatic segments and a vestigial un-segmented metasoma with a long narrow telson. 4. Genital openings paired covered by genital operculum. 5. Respiration by lamelliform gills or book- gills attached to the abdominal appendages. Example: Limulus (King crab). Subclass II. Eurypterida: 1. Extinct (Palaeozoic) forms. 2. Large sized arthropods. 3. Cephalothorax small covered by dorsal carapace. 4. Cephalothorax followed by 12 free segments and a terminal elongated narrow telson. 5. Cephalothorax with six pairs of appendages. Examples: Eurypterus, Pterygotus. Class 2. Arachnida (Gr., arachne = spider + oid = like): Class 2. Arachnida (Gr., arachne = spider + oid = like): 1. Mostly terrestrial, few aquatic. 2. Prosoma bears six pairs of appendages; one pair chelicerae one pair pedipalpi and four pairs of walking legs. 3. Abdomen usually without appendages. 4. Respiratory organs either tracheae, book- lungs or book-gills. 5. Excretory organs are Malpighian tubules or coxal glands or both. 6. Sexes are separate, sexual dimorphism not conspicuous and development mostly direct. Order 1. Scorpionida: 1. Terrestrial forms found under stones in tropical and subtropical regions; true scorpions. 2. Prosoma covered dorsally by carapace and bears a pair of chelicerae, a pair of pedipalpi and four pairs of walking legs. 3. Opisthosoma divisible into mesosoma and metasoma; mesosoma is broad consisting of seven segments and metasoma is narrow consisting of five segments with a poison- sting. 4. A pair of comb-like pectines occur ventrally on the second segment of mesosoma. 5. Respiration by four pairs of book-lungs. Examples: Buthus, Palamnaeus. Order 2. Pseudoscorpionida: 1. Minute false scorpions found under the bark of trees. 2. Prosoma formed of six fused segments covered dorsally by carapace. 3. Opisthosoma often to twelve segments. 4. Sting and telson not found. 5. A pair of spinning glands present. 6. Respiration by tracheae. Example: Chelifer. Order 3. Palpigradi: 1. Small arachnids. 2. Opisthosoma often segments and is jointed to the prosoma by a pedicle. 3. Telson with a long jointed flagellum. 4. Chelicerae are chelate and pedipalpi leg like. 5. Respiration by three pairs of book-lungs. Example: Koenenia. Order 4. Solifugae: 1. Body consists of prosoma and opisthosoma. 2. Prosoma consists of three fused and last three segments. 3. Opisthosoma composed of ten segments and is not marked off from prosoma. 4. Chelicerae are large and chelate, pedipalpi are elongated and leg-like. 5. Poison glands absent. 6. Respiration by tracheae. 7. Commonly referred to as sun spiders or wind spiders. Example: Galeodes. Order 5. Amblypygi: 1. Somewhat flattened body. 2. Carapace covering the prosoma undivided. 3. Pedipalpi large and heavy, chelicerae of moderate size. 4. First pair walking legs sensory in nature. 5. Opisthosoma bears twelve segments, flage​llum absent. Example: Charinus. Order 6. Uropygi: 1. Commonly referred to as whip scorpions. 2. Chelicerae two-jointed and moderate in size. 3. Pedipalpi large, heavy and usually with pincers. 4. Opisthosoma bears twelve segmentsa long flagellum present in the last segment. 5. Eyes one pair. Examples: Thelyphonus, Mastigoproctus. Order 7. Araneae: 1. Body consists of prosoma and opisthosoma. 2. Prosoma is unsegmented covered by cara​pace and bears six pairs of appendages. 3. Opisthosoma is usually unsegmented attached to prosoma by a narrow pedicle. 4. Chelicerae are subchelate with poison glands. 5. Pedipalps simple and six jointed. 6. Eight eyes are arranged dorsally in two rows on the carapace of prosoma. 7. Respiration either by book-lungs or book- lungs and tracheae both. 8. True spiders. Examples: Argiope (Writing spider), Aranea (House spider) Lycosa (Wolf spider), Agelena (Funnel-web spider). Order 8. Ricinulei: 1. Body consists of prosoma and opisthosoma. 2. Prosoma with movable anterior cucullus. 3. Opisthosoma composed of nine segments and connected to prosoma by a pedicle. 4. Chelicerae and pedipalpi are chelate. 5. Respiration by tracheae. Examples: Cryptocellus, Ricinoides. Order 9. Phalangida or Opiliones: 1. Spider-like in appearance. 2. Prosoma unsegmented, opisthosoma bears ten segments. 3. Pedicel absent between prosoma and opisthosoma. 4. Chelicerae chelate; pedipalpi leg-like. 5. Spinning glands not found. 6. Respiration by tracheae. Examples: Phalangium, Leiobunum. Order 10. Acarina: 1. Body unsegmented in which prosoma is fused with opisthosoma. 2. Chelicerae and pedipalpi are small and associated with the mouth-parts which are adapted for biting, piercing and sucking. 3. Respiration by tracheae or by skin. 4. Free living and parasitic forms. 5. Commonly referred to as ticks and mites. Examples: Chorioptes (Mite), Sarcoptes (Itch-mite), Idodex (Tick). Class 3. Pycnogonida: 1. Commonly referred to as sea spiders. 2. Very small in size. 3. Body mainly consists of cephalothorax, abdomen reduced. 4. Pedipalpi short segmented and chelicerae very small. 5. Usually eight pairs of long walking legs. 6. Mouth placed on a long proboscis. 7. Eyes simple and 4 in number. 8. Respiratory and excretory organs wanting. 9. Sexes separate (dioecious); females with a pair of ovigers for carrying eggs. Examples: Pycnogonum, Nymphon. Subphylum III. Mandibulata: (L., mandibula = mandible + at a = group): 1. Terrestrial and aquatic both freshwater and marine. 2. Body divisible into either cephalothhorax and abdomen or head, thorax and abdomen. 3. Appendages of head consist of one or two pairs of antennae, one pair of mandibles and one or two pairs of maxillae. 4. Eyes usually compound. 5. Respiration either by gills or tracheae. 6. Excretion by Malpighian tubules or green glands. 7. Sexes usually separate with sexual dimorphism. 8. Development usually involves larval stages. Class 1. Crustacea (L., crusta = a hard shell): 1. Mainly aquatic, generally marine but few freshwater and few live in moist places. 2. Generally free living but few are parasitic forms. 3. Head often fused with thorax to form cep​halothorax covered dorsally by carapace. 4. Head bears a pair of compound eyes and five pairs of appendages. 5. Thorax and abdomen often with a pair of biramous appendages in each segment; appendages modified for various purpose. 6. Respiration either by gills or general body surface. 7. Coelom greatly reduced, it is in the form of haemocoel. 8. Blood vascular system
Recommended publications
  • Exploring Phylogenomic Relationships Within Myriapoda: Should High Matrix Occupancy Be the Goal?
    bioRxiv preprint doi: https://doi.org/10.1101/030973; this version posted November 9, 2015. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Exploring phylogenomic relationships within Myriapoda: should high matrix occupancy be the goal? ROSA FERNÁNDEZ1, GREGORY D. EDGECOMBE2 AND GONZALO GIRIBET1 1Museum of Comparative Zoology & Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA 2Department of Earth Sciences, The Natural History Museum, Cromwell Road, London SW7 5BD, UK 1 bioRxiv preprint doi: https://doi.org/10.1101/030973; this version posted November 9, 2015. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Abstract.—Myriapods are one of the dominant terrestrial arthropod groups including the diverse and familiar centipedes and millipedes. Although molecular evidence has shown that Myriapoda is monophyletic, its internal phylogeny remains contentious and understudied, especially when compared to those of Chelicerata and Hexapoda. Until now, efforts have focused on taxon sampling (e.g., by including a handful of genes in many species) or on maximizing matrix occupancy (e.g., by including hundreds or thousands of genes in just a few species), but a phylogeny maximizing sampling at both levels remains elusive. In this study, we analyzed forty Illumina transcriptomes representing three myriapod classes (Diplopoda, Chilopoda and Symphyla); twenty-five transcriptomes were newly sequenced to maximize representation at the ordinal level in Diplopoda and at the family level in Chilopoda.
    [Show full text]
  • Ordinal-Level Phylogenomics of the Arthropod Class
    Ordinal-Level Phylogenomics of the Arthropod Class Diplopoda (Millipedes) Based on an Analysis of 221 Nuclear Protein-Coding Loci Generated Using Next- Generation Sequence Analyses Michael S. Brewer1,2*, Jason E. Bond3 1 Department of Environmental Science, Policy, and Management, University of California Berkeley, Berkeley, California, United States of America, 2 Department of Biology, East Carolina University, Greenville, North Carolina, United States of America, 3 Department of Biological Sciences and Auburn University Museum of Natural History, Auburn University, Auburn, Alabama, United States of America Abstract Background: The ancient and diverse, yet understudied arthropod class Diplopoda, the millipedes, has a muddled taxonomic history. Despite having a cosmopolitan distribution and a number of unique and interesting characteristics, the group has received relatively little attention; interest in millipede systematics is low compared to taxa of comparable diversity. The existing classification of the group comprises 16 orders. Past attempts to reconstruct millipede phylogenies have suffered from a paucity of characters and included too few taxa to confidently resolve relationships and make formal nomenclatural changes. Herein, we reconstruct an ordinal-level phylogeny for the class Diplopoda using the largest character set ever assembled for the group. Methods: Transcriptomic sequences were obtained from exemplar taxa representing much of the diversity of millipede orders using second-generation (i.e., next-generation or high-throughput) sequencing. These data were subject to rigorous orthology selection and phylogenetic dataset optimization and then used to reconstruct phylogenies employing Bayesian inference and maximum likelihood optimality criteria. Ancestral reconstructions of sperm transfer appendage development (gonopods), presence of lateral defense secretion pores (ozopores), and presence of spinnerets were considered.
    [Show full text]
  • An Apparently Non-Swinging Tentorium in the Diplopoda (Myriapoda): Comparative Morphology of the Tentorial Complex in Giant Pill-Millipedes (Sphaerotheriida)
    A peer-reviewed open-access journal ZooKeys 741: 77–91An (2018) apparently non-swinging tentorium in the Diplopoda (Myriapoda)... 77 doi: 10.3897/zookeys.741.21909 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research An apparently non-swinging tentorium in the Diplopoda (Myriapoda): comparative morphology of the tentorial complex in giant pill-millipedes (Sphaerotheriida) Leif Moritz1, Thomas Wesener1, Markus Koch2,3 1 Zoologisches Forschungsmuseum Alexander Koenig, Leibniz Institute for Animal Biodiversity, Section Myria- poda, Adenauerallee 160, 53113 Bonn, Germany 2 Institute of Evolutionary Biology and Ecology, University of Bonn, An der Immenburg 1, 53121 Bonn, Germany 3 Senckenberg Gesellschaft für Naturforschung, Dept. In- formation Technology and Biodiversity Informatics, Senckenberganlage 25, 60325 Frankfurt am Main, Germany Corresponding author: Leif Moritz ([email protected]) Academic editor: G.D. Edgecombe | Received 29 October 2017 | Accepted 20 December 2017 | Published 7 March 2018 http://zoobank.org/8F4AEFD3-9943-42D5-9E08-11C0F1D94FB4 Citation: Moritz L, Wesener T, Koch M (2018) An apparently non-swinging tentorium in the Diplopoda (Myriapoda): comparative morphology of the tentorial complex in giant pill-millipedes (Sphaerotheriida). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 77–91. https://doi.org/10.3897/zookeys.741.21909 Abstract The presence of a swinging tentorium is a key apomorphy of Myriapoda, but this character has been studied in detail in only few species. Here the tentorium, i.e., the peristomatic skeleton of the preoral chamber, is comparatively studied in three species of the millipede order Sphaerotheriida Brandt, 1833. Since dissections of the fragile tentorial components proved to be difficult, despite the large head size, they were analysed mainly in situ via micro-computed tomography.
    [Show full text]
  • Monophyly of the Ring-Forming Group in Diplopoda (Myriapoda, Arthropoda) Based on SSU and LSU Ribosomal RNA Sequences
    Available online at www.sciencedirect.com Progress in Natural Science 19 (2009) 1297–1303 www.elsevier.com/locate/pnsc Monophyly of the ring-forming group in Diplopoda (Myriapoda, Arthropoda) based on SSU and LSU ribosomal RNA sequences Peiyun Cong a,b, Xuhua Xia c, Qun Yang a,* a State Key Laboratory of Palaeobiology and Strategraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, China b Yunnan Key Laboratory for Paleobiology, Yunnan University, Kunming 650091, China c Department of Biology, University of Ottawa, Ont., Canada K1N 6N5 Received 13 February 2009; received in revised form 15 March 2009; accepted 17 March 2009 Abstract Two controversies exist in the phylogeny of the derived millipedes (Diplopoda). The first is whether millipedes with a fusion ring, including Polydesmida, Spirobolida, Spirostreptida and Julida, form a monophyletic group (the ring-forming group). The second con- cerns the phylogenetic relationship within the three orders of Juliformia, i.e. Julida, Spirostreptida and Spirobolida. To resolve these phylogenetic controversies, we sequenced 18S and 28S rDNA from six millipede orders and retrieved several homologous sequences from GenBank. Our results give robust support to the monophyly of the ring-forming group based on maximum parsimony methods, max- imum likelihood methods and Bayesian inference. The monophyly of the ring-forming group suggests that the fusion of segment sclerites might have occurred only once during millipede evolutionary history. We also established a sister-group relationship between Spirobol- ida and Spirostreptida within Juliformia after eliminating a short-branch attraction phenomenon, which is consistent with that from the mitochondrial genome analysis.
    [Show full text]
  • Redescription of the South African Millipede Cylichnogaster Lawrencei Verhoeff, 1937 and Notes on the Family Siphonotidae (Diplopoda, Polyzoniida)
    Zootaxa 4079 (1): 119–128 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4079.1.8 http://zoobank.org/urn:lsid:zoobank.org:pub:9A6185BE-9CDB-40A3-90DD-9D36A797AEC8 Redescription of the South African millipede Cylichnogaster lawrencei Verhoeff, 1937 and notes on the family Siphonotidae (Diplopoda, Polyzoniida) WILLIAM A. SHEAR Emeritus Professor, Department of Biology, Hampden-Sydney College, Hampden-Sydney VA 23943 USA Abstract The unusual millipede Cylichnogaster lawrencei Verhoeff, 1937 (Diplopoda, Polyzoniida, Siphonotidae) is redescribed from newly collected specimens. Species of Cylichnogaster are the only known colobognathan millipedes capable of vol- vation, and are also distinguished by their small size and low segment number. Taxonomic notes are provided on the poorly known family Siphonotidae. Key words: Cylichnogaster nigricornis, Siphonotus, Burinia, Rhinotus, volvation, South Africa, Table Mountain Introduction The millipede genus Cylichnogaster was established by Verhoeff in 1937 for the single species C. lawrencei, from the Cape Peninsula, South Africa. A second species, C. nigricornis, also South African, was added by Schubart in 1966. These two species are perhaps the most distinctive of all members of the millipede subterclass Colobognatha, since they are capable of more or less complete volvation, or enrollment, with reduced numbers of highly arched trunk segments that allow them to defend themselves by rolling up into a ball. When in this form, the legs, head and antennae of the millipedes are well protected, concealed beneath the tergites. Other members of the Colobognatha can at best curl into a tight spiral in which the head and antennae are in the center, but still exposed.
    [Show full text]
  • Diplopoda — Taxonomic Overview
    CHAPTER 16 DIPLOPODA — TAXONOMIC OVERVIEW BY HENRIK ENGHOFF, SERGEI GOLOVATCH, MEGAN SHORT, PAVEL STOEV AND THOMAS WESENER There is no widely accepted consensus about the classification of Diplopoda. The following account basically follows the arrangement by Shear (2011), deviations from this are specified. All currently recognized families are mentioned, and more or less exact numbers of known genera and species in each family are given, as well as the known geographical distribution. With more than 1800 recognized genera (1868 according to Shear, 2011) mentioning and characterizing them all would require a volume in itself. In the following treatment, which is exhaustive down to the families, all genera are mentioned only for some, mainly smaller orders, whereas only a selection of genera are mentioned for the large orders Polydesmida, Chordeumatida, Julida and Spirostreptida. Likewise, the amount of morphological detail varies greatly between orders, and this chapter cannot in general be used as an identification manual. For those genera which are listed, the (approximate) number of known species and the geographical distribution are given, and as a rule the name of at least one species per listed genus is included. Information on habits is included to a limited extent, e.g., if the members of the family/genus are cavernicolous. Only Recent taxa are treated here. For fossils see Chapter 14. Class DIPLOPODA de Blainville in Gervais, 1844 [HENRIK ENGHOFF] Terrestrial mandibulate and tracheate arthropods with adult body size 1.4-350 mm. Cuticle rarely soft and covered by modified setae (Polyxenida), usually calcified, form- ing an inflexible, rarely flexible (Glomeridesmida and Polyzoniida), exoskeleton.
    [Show full text]
  • The Myriapoda of Halimun-Salak National Park (Java, Indonesia): Overview and Faunal Composition
    Biodiversity Data Journal 7: e32218 doi: 10.3897/BDJ.7.e32218 Research Article The Myriapoda of Halimun-Salak National Park (Java, Indonesia): overview and faunal composition Michael Hilgert‡§, Nesrine Akkari , Cahyo Rahmadi|,¶, Thomas Wesener# ‡ Rheinische Friedrich-Wilhelms-Universität, Bonn, Germany § Naturhistorisches Museum Wien, Wien, Austria | Indonesian Institute of Sciences, Cibinong, Indonesia ¶ Indonesia Speleological Society, Bogor, Indonesia # Zoological Research Museum A. Koenig, Leibniz Institue for Animal Biodiversity, Bonn, Germany Corresponding author: Thomas Wesener ([email protected]) Academic editor: Pavel Stoev Received: 06 Dec 2018 | Accepted: 04 Apr 2019 | Published: 15 Apr 2019 Citation: Hilgert M, Akkari N, Rahmadi C, Wesener T (2019) The Myriapoda of Halimun-Salak National Park (Java, Indonesia): overview and faunal composition. Biodiversity Data Journal 7: e32218. https://doi.org/10.3897/BDJ.7.e32218 Abstract The myriapod fauna of the mega-diverse country of Indonesia is so far insufficiently known, with no species lists or determination keys. In order to obtain an overview of the faunal composition of the Myriapoda in an Indonesian forest system, the fauna of the Halimun- Salak National Park in western Java was explored during the dry season (September– October 2015) in the framework of the German-Indonesian INDOBIOSYS project (Indonesian Biodiversity Discovery and Information System). A total of 980 Myriapoda specimens were collected by hand by 3–4 researchers from three different sites in the national park, from which 796 specimens were determined to a higher taxonomic level (class, order, family) and 617 specimens were determined to morphospecies. Among these, 27 were Symphyla (4%) (excluded from further analyses), 226 Chilopoda (28%) and 543 Diplopoda (68%).
    [Show full text]
  • Diversity and Function of Fungi Associated with the Fungivorous Millipede, Brachycybe
    bioRxiv preprint doi: https://doi.org/10.1101/515304; this version posted January 9, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Diversity and function of fungi associated with the fungivorous millipede, Brachycybe lecontii † Angie M. Maciasa, Paul E. Marekb, Ember M. Morrisseya, Michael S. Brewerc, Dylan P.G. Shortd, Cameron M. Staudera, Kristen L. Wickerta, Matthew C. Bergera, Amy M. Methenya, Jason E. Stajiche, Greg Boycea, Rita V. M. Riof, Daniel G. Panaccionea, Victoria Wongb, Tappey H. Jonesg, Matt T. Kassona,* a Division of Plant and Soil Sciences, West Virginia University, Morgantown, WV, 26506, USA b Department of Entomology, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA c Department of Biology, East Carolina University, Greenville, NC 27858, USA d Amycel Spawnmate, Royal Oaks, CA, 95067, USA e Department of Microbiology and Plant Pathology and Institute for Integrative Genome Biology, University of California, Riverside, CA 92521, USA f Department of Biology, West Virginia University, Morgantown, WV, 26506, USA g Department of Chemistry, Virginia Military Institute, Lexington, VA, 24450, USA † Scientific article No. XXXX of the West Virginia Agricultural and Forestry Experiment Station, Morgantown, West Virginia, USA, 26506. * Corresponding author. Current address: G103 South Agricultural Sciences Building, Morgantown, WV, 26506, USA. E-mail address: [email protected] (M.T. Kasson). bioRxiv preprint doi: https://doi.org/10.1101/515304; this version posted January 9, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder.
    [Show full text]
  • Putative Apomorphies of Millipede Clades; Page - 1
    Milli-PEET, Putative apomorphies of millipede clades; Page - 1 - Defining Features of Nominal Clades of Diplopoda Morphological descriptions of various millipede groupings are scattered in several works, span over 100 years and several languages. A critical compilation identifying putative apomorphies is needed since some of these morphological features are employed in various discussions on diplopod and myriapod phylogeny. For each nominal clade, we give putative morphological autapomorphies (PA), distinguished from other characters (OC), which may help to recognize the group. The morphological features that may represent putative apomorphies are often known from only a handful of species; a thorough taxon sampling with regards to these characters is required. The listing of the nominal clades follows the currently assumed phylogenetic hierarchy (see Figures 2 and 4 on the Milli-PEET web site, Page: Millipede Systematics). Abbreviations: TO=Tömösvary organ, LP= leg pair; BR=Body ring(s); LTS=median longitudinal tergite suture; S-T= sperm transferring. Pauropoda. – PA: branched antennae with segmented stalk and unique sense organ (Globulus). Putative synapomorphies with Diplopoda: collum segment (with leg rudiments in Pauropoda); dignath condition, Maxille1 forming a gnathochlarium-like plate; tracheal system (only in the Hexamerocerata). OC: TO present (called Pseudoculus in Pauropoda); ocelli absent; some tergites enlarged, covering two segments; 9-11 leg-bearing trunk segments; animals small. Diplopoda. – PA: diplosegements of the trunk; legless collum segment; four antennal sense cones; aflagellate sperm. Field Museum of Natural History, updated 26 September 2006 Milli-PEET, Putative apomorphies of millipede clades; Page - 2 - Penicillata (Pselaphognatha, bristle millipedes). – PA: serrated setae arranged in tufts; head with transverse suture between antennae and ocellar clusters.
    [Show full text]
  • Diplopoda: Julida) Rowland M
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 10-21-2016 Parajulid milliped studies XI: Initial assessment of the tribe Gosiulini (Diplopoda: Julida) Rowland M. Shelley University of Tennessee, Knoxville, [email protected] Jamie M. Smith Franklinton, NC, [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons, and the Population Biology Commons Shelley, Rowland M. and Smith, Jamie M., "Parajulid milliped studies XI: Initial assessment of the tribe Gosiulini (Diplopoda: Julida)" (2016). Insecta Mundi. 1014. http://digitalcommons.unl.edu/insectamundi/1014 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 A Journal of World Insect Systematics 0509 Parajulid milliped studies XI: Initial assessment of the tribe Gosiulini (Diplopoda: Julida) Rowland M. Shelley Department of Entomology and Plant Pathology University of Tennessee 2505 E J Chapman Dr. Knoxville, TN 37996-4560 USA Jamie M. Smith 425 Phelps Rd. Franklinton, NC 27525 USA Date of Issue: October 21, 2016 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Rowland M. Shelley and Jamie M. Smith Parajulid milliped studies XI: Initial assessment of the tribe Gosiulini (Diplopoda: Julida) Insecta Mundi 0509: 1–17 ZooBank Registered: urn:lsid:zoobank.org:pub:C8A2163D-6684-4F7F-9D51-9E6D4FC8F9A0 Published in 2016 by Center for Systematic Entomology, Inc. P. O. Box 141874 Gainesville, FL 32614-1874 USA http://centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non-marine arthropod.
    [Show full text]
  • Natural History of the Social Millipede Brachycybe Lecontii (Wood, 1864)
    Natural history of the social millipede Brachycybe lecontii (Wood, 1864) Victoria Louise Wong Thesis submitted to the faculty of the Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Master of Science in Entomology Paul Marek Carlyle Brewster Robin Andrews December 1, 2017 Blacksburg, VA Keywords: Brachycybe lecontii, diplopoda, millipede, natural history Copyright 2017, Victoria L. Wong Natural history of the social millipede Brachycybe lecontii (Wood, 1864) Victoria Louise Wong Scientific Abstract The millipede Brachycybe lecontii Wood, 1864 is a social millipede known for forming pinwheel- shaped groups and for paternal care of eggs. Brachycybe lecontii is endemic to the eastern U.S., and its distribution overlaps with another species within the genus, Brachycybe petasata, from the Southern Appalachian Mountains. Molecular data, however, show that the closest relative of B. lecontii is Brachycybe nodulosa from East Asia. Here, I investigated various aspects of the life history, paternal care, defense, feeding, and social behavior of B. lecontii, and provided morphological and anatomical descriptions using light and scanning electron microscopy. Based on detailed observations of millipedes from 14 localities in the distribution of B. lecontii, I found the following natural history aspects. The oviposition period of B. lecontii was from mid-April to late June and the incubation period lasted 3–4 weeks. Males exclusively cared for eggs, but care of juveniles was not observed. In one case, the clutches of two males became combined and they were later cared for by only one of the males. The defensive compound of B. lecontii consisted of two isomers of the alkaloid deoxybuzonamine.
    [Show full text]
  • Diplopoda: Platydesmida: Andrognathidae)
    Organisms Diversity & Evolution (2019) 19:423–433 https://doi.org/10.1007/s13127-019-00408-0 ORIGINAL ARTICLE The first known fossils of the Platydesmida—an extant American genus in Cretaceous amber from Myanmar (Diplopoda: Platydesmida: Andrognathidae) Leif Moritz1 & Thomas Wesener1 Received: 19 January 2019 /Accepted: 20 June 2019 /Published online: 29 June 2019 # Gesellschaft für Biologische Systematik 2019 Abstract Millipedes have been inhabiting the earth for more than 400 my and show a great diversity regarding their morphology and ecology. For a better understanding of the timing and pattern of millipede evolution, Burmese amber offers a unique window into the Cretaceous period, ca. 99 Ma. Here, we describe the first known fossil of the colobognathan order Platydesmida, the species Andrognathus burmiticus n. sp. based on 15 specimens from Cretaceous Burmese amber. We combine classical light-microscopy and modern micro-computer tomography (μCT) with computer aided 3D-reconstructions. These non-invasive techniques allow us to describe the fossil millipedes as detailed as is general practice for extant species, and to grant the scientific community open access to the deposited “Cybertypes”. Based on the combination of unique morphological characters such as surface structures, body type, the unique size and shape of tergite 5, the absence of a hypoproct at the anal segment, and detailed gonopod characteristics, the studied fossils can be placed in the family Andrognathidae and the extant genus Andrognathus, which nowadays is restricted to the eastern USA and Mexico with three extant species. Therefore, the minimum age of the genus Andrognathus is pushed to the Cenomanian, 99 Ma. It can be assumed that the genus was much more diverse and wider distributed in the past and migrated between Asia and America via one of the once existing land bridges.
    [Show full text]