A Callipodidan Cocoon (Diplopoda, Callipodida, Schizopetalidae)
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Millipedes (Diplopoda) from Caves of Portugal
A.S.P.S. Reboleira and H. Enghoff – Millipedes (Diplopoda) from caves of Portugal. Journal of Cave and Karst Studies, v. 76, no. 1, p. 20–25. DOI: 10.4311/2013LSC0113 MILLIPEDES (DIPLOPODA) FROM CAVES OF PORTUGAL ANA SOFIA P.S. REBOLEIRA1 AND HENRIK ENGHOFF2 Abstract: Millipedes play an important role in the decomposition of organic matter in the subterranean environment. Despite the existence of several cave-adapted species of millipedes in adjacent geographic areas, their study has been largely ignored in Portugal. Over the last decade, intense fieldwork in caves of the mainland and the island of Madeira has provided new data about the distribution and diversity of millipedes. A review of millipedes from caves of Portugal is presented, listing fourteen species belonging to eight families, among which six species are considered troglobionts. The distribution of millipedes in caves of Portugal is discussed and compared with the troglobiont biodiversity in the overall Iberian Peninsula and the Macaronesian archipelagos. INTRODUCTION All specimens from mainland Portugal were collected by A.S.P.S. Reboleira, while collectors of Madeiran speci- Millipedes play an important role in the decomposition mens are identified in the text. Material is deposited in the of organic matter, and several species around the world following collections: Zoological Museum of University of have adapted to subterranean life, being found from cave Copenhagen, Department of Animal Biology, University of entrances to almost 2000 meters depth (Culver and Shear, La Laguna, Spain and in the collection of Sofia Reboleira, 2012; Golovatch and Kime, 2009; Sendra and Reboleira, Portugal. 2012). Although the millipede faunas of many European Species were classified according to their degree of countries are relatively well studied, this is not true of dependence on the subterranean environment, following Portugal. -
Supra-Familial Taxon Names of the Diplopoda Table 4A
Milli-PEET, Taxonomy Table 4 Page - 1 - Table 4: Supra-familial taxon names of the Diplopoda Table 4a: List of current supra-familial taxon names in alphabetical order, with their old invalid counterpart and included orders. [Brackets] indicate that the taxon group circumscribed by the old taxon group name is not recognized in Shelley's 2003 classification. Current Name Old Taxon Name Order Brannerioidea in part Trachyzona Verhoeff, 1913 Chordeumatida Callipodida Lysiopetalida Chamberlin, 1943 Callipodida [Cambaloidea+Spirobolida+ Chorizognatha Verhoeff, 1910 Cambaloidea+Spirobolida+ Spirostreptida] Spirostreptida Chelodesmidea Leptodesmidi Brölemann, 1916 Polydesmida Chelodesmidea Sphaeriodesmidea Jeekel, 1971 Polydesmida Chordeumatida Ascospermophora Verhoeff, 1900 Chordeumatida Chordeumatida Craspedosomatida Jeekel, 1971 Chordeumatida Chordeumatidea Craspedsomatoidea Cook, 1895 Chordeumatida Chordeumatoidea Megasacophora Verhoeff, 1929 Chordeumatida Craspedosomatoidea Cheiritophora Verhoeff, 1929 Chordeumatida Diplomaragnoidea Ancestreumatoidea Golovatch, 1977 Chordeumatida Glomerida Plesiocerata Verhoeff, 1910 Glomerida Hasseoidea Orobainosomidi Brolemann, 1935 Chordeumatida Hasseoidea Protopoda Verhoeff, 1929 Chordeumatida Helminthomorpha Proterandria Verhoeff, 1894 all helminthomorph orders Heterochordeumatoidea Oedomopoda Verhoeff, 1929 Chordeumatida Julida Symphyognatha Verhoeff, 1910 Julida Julida Zygocheta Cook, 1895 Julida [Julida+Spirostreptida] Diplocheta Cook, 1895 Julida+Spirostreptida [Julida in part[ Arthrophora Verhoeff, -
MYRIAPODS 767 Volume 2 (M-Z), Pp
In: R. Singer, (ed.), 1999. Encyclopedia of Paleontology, MYRIAPODS 767 volume 2 (M-Z), pp. 767-775. Fitzroy Dearborn, London. MYRIAPODS JVlyriapods are many-legged, terrestrial arthropods whose bodies groups, the Trilobita, Chelicerata, Crustacea, and the Uniramia, the are divided into two major parts, a head and a trunk. The head last consisting of the Myriapoda, Hexapoda, and Onychophora (vel- bears a single pair of antennae, highly differentiated mandibles (or vet worms). However, subsequent structural and molecular evidence jaws), and at least one pair of maxillary mouthparts; the trunk indicates that there are several characters uniting major arthropod region consists of similar "metameres," each of which is a func- taxa. Moreover, paleobiologic, embryologie, and other evidence tional segment that bears one or two pairs of appendages. Gas demonstrates that myriapods and hexapods are fiindamentally exchange is accomplished by tracheae•a branching network of polyramous, having two major articulating appendages per embry- specialized tubules•although small forms respire through the ological body segment, like other arthropods. body wall. Malpighian organs are used for excretion, and eyes con- A fourth proposal (Figure ID) suggests that myriapods are sist of clusters of simple, unintegrated, light-sensitive elements an ancient, basal arthropod lineage, and that the Hexapoda that are termed ommatidia. These major features collectively char- emerged as an independent, relatively recent clade from a rather acterize the five major myriapod clades: Diplopoda (millipeds), terminal crustacean lineage, perhaps the Malacostraca, which con- Chilopoda (centipeds), Pauropoda (pauropods), Symphyla (sym- tains lobsters and crabs (Ballard et al. 1992). Because few crusta- phylans), and Arthropleurida (arthropleurids). Other features cean taxa were examined in this analysis, and due to the Cambrian indicate differences among these clades. -
Anamorphic Development of Apfelbeckia Insculpta (L. Koch, 1867) (Diplopoda: Callipodida: Schizopetalidae)
Arch Biol Sci. 2016;68(2):445-450 DOI:10.2298/ABS150802128I ANAMORPHIC DEVELOPMENT OF APFELBECKIA INSCULPTA (L. KOCH, 1867) (DIPLOPODA: CaLLIPODIDA: SCHIZOPETALIDAE) Bojan S. Ilić*, Vladimir T. Tomić, Luka R. Lučić and Bojan M. Mitić University of Belgrade – Faculty of Biology, Institute of Zoology, Studentski Trg 16, 11000 Belgrade, Serbia *Corresponding author: [email protected] Received: August 2, 2015; Revised: September 3, 2015; Accepted: September 16, 2015; Published online: November 3; 2015 Abstract: An overview of the anamorphic development of Apfelbeckia insculpta is provided. As in other myriapods and arthropods, post-embryonic period of the life cycle includes different stages that are separated by molts. Based on an earlier description of post-embryogenesis of A. insculpta and on our data, we describe ten stadia that occur after juveniles of our focal species hatch from the egg. Each molt is accompanied by the addition of podous and apodous pleurotergites, leg-pairs and ocelli. Thus, the numbers of these structures can be used as reliable criteria for the separation of post-embryonic sta- dia in A. insculpta. Adulthood is reached through teloanamorphosis, i.e., with the ninth and last molt individuals become sexually mature and achieve adulthood. Sexes can be distinguished from stadium VIII onward. Key words: Apfelbeckia insculpta; post-embryonic development; teloanamorphosis INTRODUCTION modes of anamorphosis are recognized in Diplopoda: euanamorphosis, hemianamorphosis, and teloan- Most millipedes can be described as multi-segmented amorphosis [4-6]. In euanamorphosis (recognized in and multi-legged animals. However, newly hatched Julida and Colobognatha), animals molt throughout millipedes usually have a significantly lower number life and every molt is accompanied by the addition of segments and legs than adults and the final, or adult of new segments. -
Full Issue, Vol. 57 No. 3
Great Basin Naturalist Volume 57 Number 3 Article 15 7-31-1997 Full Issue, Vol. 57 No. 3 Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation (1997) "Full Issue, Vol. 57 No. 3," Great Basin Naturalist: Vol. 57 : No. 3 , Article 15. Available at: https://scholarsarchive.byu.edu/gbn/vol57/iss3/15 This Full Issue is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. T H E GREAT BASBASINI1 naturalistnaturalist ale A VOLUME 57 ngN 3 JULY 1997 BRIGHAM YOUNG university GREAT BASIN naturalist editor assistant editor RICHARD W BAUMANN NATHAN M SMITH 290 MLBM 190 MLBM PO box 20200 PO box 26879 brigham youhgyoung university brigham young university provo UT 84602020084602 0200 provo UT 84602687984602 6879 8013785053801 378 5053 8017378801378668880173786688801 378 6688 FAX 8013783733801 378 3733 emailE mail nmshbllibyuedunmshbll1byuedu associate editors J R CALLAHAN PAUL C MARSH museum of southwestern biology university of tentercentergenter for environmental studies arizona new mexico albuquerque NM state university tempe AZ 85287 mailing address box 3140 hemet CA 92546 STANLEY D SMITH BRUCE D ESHELMAN department of biology department of Biologicbiologicalajlainaln sciences university of university of nevada las vegas wisconsin whitewawhitewaterwhitewayterten -
The Biological Resources of Illinois Caves and Other
I LLINOI S UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN PRODUCTION NOTE University of Illinois at Urbana-Champaign Library Large-scale Digitization Project, 2007. EioD THE BIOLOGICAL RESOURCES OF ILLINOIS CAVES AND OTHER SUBTERRANEAN ENVIRONMENTS Determination of the Diversity, Distribution, and Status of the Subterranean Faunas of Illinois Caves and How These Faunas are Related to Groundwater Quality Donald W. Webb, Steven J. Taylor, and Jean K. Krejca Center for Biodiversity Illinois Natural History Survey 607 East Peabody Drive Champaign, Illinois 61820 (217) 333-6846 TECHNICAL REPORT 1993 (8) ILLINOIS NATURAL HISTORY SURVEY CENTER FOR BIODIVERSITY Prepared for: The Environmental Protection Trust Fund Commission and Illinois Department of Energy and Natural Resources Office of Research and Planning 325 W. Adams, Room 300 Springfield, IL 62704-1892 Jim Edgar, Governor John Moore, Director State of Illinois Illinois Department of Energy and Natural Resources ACKNOWLEDGEMENTS Funding for this project was provided through Grant EPTF23 from the Environmental Protection Trust Fund Commission, administered by the Department of Energy and Natural Resources (ENR). Our thanks to Doug Wagner and Harry Hendrickson (ENR) for their assistance. Other agencies that contributed financial support include the Shawnee National Forest (SNF) and the Illinois Department of Transportation (IDOT). Many thanks to Mike Spanel (SNF) and Rich Nowack (IDOT) for their assistance. Several agencies cooperated in other ways; we are. grateful to: Illinois Department of Conservation (IDOC); Joan Bade of the Monroe-Randolph Bi- County Health Department; Russell Graham and Jim Oliver, Illinois State Museum (ISM); Dr. J. E. McPherson, Zoology Department, Southern Illinois University at Carbondale (SIUC). Further contributions were made by the National Speleological Society, Little Egypt and Mark Twain Grottoes of the National Speleological Society, and the Missouri Speleological Survey. -
Millipedes and Centipedes? Millipedes and Centipedes Are Both Arthropods in the Subphylum Myriapoda Meaning Many Legs
A Teacher’s Resource Guide to Millipedes & Centipedes Compiled by Eric Gordon What are millipedes and centipedes? Millipedes and centipedes are both arthropods in the subphylum Myriapoda meaning many legs. Although related to insects or “bugs”, they are not actually insects, which generally have six legs. How can you tell the difference between millipedes and centipedes? Millipedes have two legs per body segment and are typically have a body shaped like a cylinder or rod. Centipedes have one leg per body segment and their bodies are often flat. Do millipedes really have a thousand legs? No. Millipedes do not have a thousand legs nor do all centipedes have a hundred legs despite their names. Most millipedes have from 40-400 legs with the maximum number of legs reaching 750. No centipede has exactly 100 legs (50 pairs) since centipedes always have an odd number of pairs of legs. Most centipedes have from 30- 50 legs with one order of centipedes (Geophilomorpha) always having much more legs reaching up to 350 legs. Why do millipedes and centipedes have so many legs? Millipedes and centipedes are metameric animals, meaning that their body is divided into segments most of which are completely identical. Metamerization is an important phenomenon in evolution and even humans have a remnant of former metamerization in the repeating spinal discs of our backbone. Insects are thought to have evolved from metameric animals after specializing body segments for specific functions such as the head for sensation and the thorax for locomotion. Millipedes and centipedes may be evolutionary relatives to the ancestor of insects and crustaceans. -
A Review of the Millipede Genus Sinocallipus Zhang, 1993 (Diplopoda, Callipodida, Sinocallipodidae), with Notes on Gonopods Monotony Vs
A peer-reviewed open-access journal ZooKeys 90: 13–34 (2011) Review of genus Sinocallipus 13 doi: 10.3897/zookeys.90.1291 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research A review of the millipede genus Sinocallipus Zhang, 1993 (Diplopoda, Callipodida, Sinocallipodidae), with notes on gonopods monotony vs. peripheral diversity in millipedes Pavel Stoev1,†, Henrik Enghoff 2,‡ 1 National Museum of Natural History, 1, Tsar Osvoboditel Blvd, 1000 Sofi a and Pensoft Publishers, 13a, Geo Milev Str., 1111 Sofi a, Bulgaria 2 Natural History Museum of Denmark (Zoological Museum), University of Copenhagen, Universitetsparken 15, DK-2100 København Ø, Denmark † urn:lsid:zoobank.org:author:333ECF33-329C-4BC2-BD6A-8D98F6E340D4 ‡ urn:lsid:zoobank.org:author:9B9D901F-D6C8-4BCA-B11B-CF6EE85B16DC Corresponding author : Pavel Stoev ( [email protected] ) Academic editor: Robert Mesibov | Received 21 March 2011 | Accepted 29 March 2011 | Published 14 April 2011 urn:lsid:zoobank.org:pub:A2B3DB26-59B7-4C7C-947E-4782EF5CF648 Citation: Stoev P, Enghoff H (2011) A review of the millipede genus Sinocallipus Zhang, 1993 (Diplopoda, Callipodida, Sinocallipodidae), with notes on gonopods monotony vs. peripheral diversity in millipedes. ZooKeys 90 : 13 – 34 . doi: 10.3897/zookeys.90.1291 Abstract Th e millipede genus Sinocallipus is reviewed, with four new cave-dwelling species, S. catba, S. deharvengi, S. jaegeri and S. steineri, being described from caves in Laos and Vietnam. With the new records the num- ber of species in the genus reaches six and the genus range is extended to Central Vietnam and North and Central Laos. Both, S. jaegeri from Khammouan Province in Laos and S. -
Order CALLIPODIDA Manual Versión Española
Revista IDE@ - SEA, nº 25B (30-06-2015): 1–12. ISSN 2386-7183 1 Ibero Diversidad Entomológica @ccesible www.sea-entomologia.org/IDE@ Class: Diplopoda Order CALLIPODIDA Manual Versión española CLASS DIPLOPODA Order Callipodida Jörg Spelda Bavarian State Collection of Zoology Münchhausenstraße 21, 81247 Munich, Germany [email protected] 1. Brief characterization of the group and main diagnostic characters 1.1. Morphology The members of the order Callipodida are best recognized by their putative apomorphies: a divided hypoproct, divided anal valves, long extrusible tubular vulvae, and, as in all other helminthomorph milli- pede orders, a characteristic conformation of the male gonopods. As in Polydesmida, only the first leg pair of the 7th body ring is transformed into gonopods, which are retracted inside the body. Body rings are open ventrally and are not fused with the sternites, leaving the coxae of the legs free. Legs in the anterior half of the body carry coxal pouches. The small collum does not overlap the head. Callipodida are of uniformly cylindrical external appearance. The number of body rings is only sometimes fixed in species and usually exceeds 40. There are nine antennomeres, as the 2nd antennomere of other Diplopoda is subdivided (= antennomere 2 and 3 in Callipodida). The general struc- ture of the gnathochilarium is shared with the Chordeumatida and Polydesmida. Callipodida are said to be characterised by longitudinal crests, which gives the order the common name “crested millipedes”. Although crest are present in most species, some genera (e.g. Schizopetalum) lack a crest, while some Spirostreptida ( e.g. in Cambalopsidae, ‘Trachystreptini’) and some Julida (e.g. -
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. -
University of Copenhagen
Myriapods (Myriapoda). Chapter 7.2 Stoev, Pavel; Zapparoli, Marzio; Golovatch, Sergei; Enghoff, Henrik; Akkari, Nasrine; Barber, Anthony Published in: BioRisk DOI: 10.3897/biorisk.4.51 Publication date: 2010 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Stoev, P., Zapparoli, M., Golovatch, S., Enghoff, H., Akkari, N., & Barber, A. (2010). Myriapods (Myriapoda). Chapter 7.2. BioRisk, 4(1), 97-130. https://doi.org/10.3897/biorisk.4.51 Download date: 07. apr.. 2020 A peer-reviewed open-access journal BioRisk 4(1): 97–130 (2010) Myriapods (Myriapoda). Chapter 7.2 97 doi: 10.3897/biorisk.4.51 RESEARCH ARTICLE BioRisk www.pensoftonline.net/biorisk Myriapods (Myriapoda) Chapter 7.2 Pavel Stoev1, Marzio Zapparoli2, Sergei Golovatch3, Henrik Enghoff 4, Nesrine Akkari5, Anthony Barber6 1 National Museum of Natural History, Tsar Osvoboditel Blvd. 1, 1000 Sofi a, Bulgaria 2 Università degli Studi della Tuscia, Dipartimento di Protezione delle Piante, via S. Camillo de Lellis s.n.c., I-01100 Viterbo, Italy 3 Institute for Problems of Ecology and Evolution, Russian Academy of Sciences, Leninsky prospekt 33, Moscow 119071 Russia 4 Natural History Museum of Denmark (Zoological Museum), University of Copen- hagen, Universitetsparken 15, DK-2100 Copenhagen, Denmark 5 Research Unit of Biodiversity and Biology of Populations, Institut Supérieur des Sciences Biologiques Appliquées de Tunis, 9 Avenue Dr. Zouheir Essafi , La Rabta, 1007 Tunis, Tunisia 6 Rathgar, Exeter Road, Ivybridge, Devon, PL21 0BD, UK Corresponding author: Pavel Stoev ([email protected]) Academic editor: Alain Roques | Received 19 January 2010 | Accepted 21 May 2010 | Published 6 July 2010 Citation: Stoev P et al. -
Journal of Cave and Karst Studies
June 2020 Volume 82, Number 2 JOURNAL OF ISSN 1090-6924 A Publication of the National CAVE AND KARST Speleological Society STUDIES DEDICATED TO THE ADVANCEMENT OF SCIENCE, EDUCATION, EXPLORATION, AND CONSERVATION Published By BOARD OF EDITORS The National Speleological Society Anthropology George Crothers http://caves.org/pub/journal University of Kentucky Lexington, KY Office [email protected] 6001 Pulaski Pike NW Huntsville, AL 35810 USA Conservation-Life Sciences Julian J. Lewis & Salisa L. Lewis Tel:256-852-1300 Lewis & Associates, LLC. [email protected] Borden, IN [email protected] Editor-in-Chief Earth Sciences Benjamin Schwartz Malcolm S. Field Texas State University National Center of Environmental San Marcos, TX Assessment (8623P) [email protected] Office of Research and Development U.S. Environmental Protection Agency Leslie A. North 1200 Pennsylvania Avenue NW Western Kentucky University Bowling Green, KY Washington, DC 20460-0001 [email protected] 703-347-8601 Voice 703-347-8692 Fax [email protected] Mario Parise University Aldo Moro Production Editor Bari, Italy [email protected] Scott A. Engel Knoxville, TN Carol Wicks 225-281-3914 Louisiana State University [email protected] Baton Rouge, LA [email protected] Exploration Paul Burger National Park Service Eagle River, Alaska [email protected] Microbiology Kathleen H. Lavoie State University of New York Plattsburgh, NY [email protected] Paleontology Greg McDonald National Park Service Fort Collins, CO The Journal of Cave and Karst Studies , ISSN 1090-6924, CPM [email protected] Number #40065056, is a multi-disciplinary, refereed journal pub- lished four times a year by the National Speleological Society.