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Scolopocryptops Zhijinensis Sp.N. and a Key to Species of Scolopocryptopine Centipedes from China (Scolopendromorpha: Scolopocryptopidae)
Arthropoda Selecta 30(1): 28–33 © ARTHROPODA SELECTA, 2021 Scolopocryptops zhijinensis sp.n. and a key to species of scolopocryptopine centipedes from China (Scolopendromorpha: Scolopocryptopidae) Scolopocryptops zhijinensis sp.n. è êëþ÷ äëÿ âèäîâ ñêîëîïîêðèïòîïèíîâûõ ãóáîíîãèõ èç Êèòàÿ (Scolopendromorpha: Scolopocryptopidae) Sha Qiao, Shu-Qing Xiao, Zhi-Yong Di Øà Êüÿî, Øó-Êèí Ñÿî, Æè-¨í Äè School of Life Sciences, Institute of Life Sciences and Green Development, Hebei University, Baoding 071002, Hebei, China; Email: [email protected] KEY WORDS: Cave, Chilopoda, taxonomy, new species, Guizhou, southern China. КЛЮЧЕВЫЕ СЛОВА: Пещера, Chilopoda, новый вид, Гижу, Юэный Китай. ABSTRACT. Scolopocryptops zhijinensis sp.n., a на Восточной Бразилии. Оба вида имеют такие сход- new scolopocryptopine centipede species, is described ные трогломорфные черты, как депигментирован- from a karst cave in Guizhou Province, China. By its ные покровы и длинные конечности. У S. zhijinensis morphological characters, S. zhijinensis sp.n. is close sp.n. членики усиков приземистые, лишь один ба- to S. troglocaudatus Chagas et Bichuette, 2015, a tro- зальный членик с редкими щетинками, а прочие globite from a siliciclastic area of eastern Brazil. They сегменты с густыми; передний край ногочелюстно- share similar troglomorphic features, such as depig- го коксостернума прямой, а зубные пластинки уз- mentation and long appendages. In S. zhijinensis sp.n., кие и не сросшиеся по средней линии; тергит пос- the antennal segments are stout, only one basal article леднего -
INSECTA MUNDIA Journal of World Insect Systematics
INSECTA MUNDI A Journal of World Insect Systematics 0573 A fourth account of centipede (Chilopoda) predation on bats T. Todd Lindley 3300 Teton Lane Norman, OK 73072 USA Jesús Molinari Departamento de Biología Universidad de Los Andes Mérida 5101 Venezuela Rowland M. Shelley Department of Entomology and Plant Pathology University of Tennessee Knoxville, TN 37996 USA Barry N. Steger 107 Saint James Street Borger, TX 79007 USA Date of Issue: August 25, 2017 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL T. Todd Lindley, Jesús Molinari, Rowland M. Shelley, and Barry N. Steger A fourth account of centipede (Chilopoda) predation on bats Insecta Mundi 0573: 1–4 ZooBank Registered: urn:lsid:zoobank.org:pub:53C2B8CA-DB7E-4921-94C5-0CA7A8F7A400 Published in 2017 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. Topics considered for publication include systematics, taxonomy, nomenclature, checklists, faunal works, and natural history. Insecta Mundi will not consider works in the applied sciences (i.e. medical entomology, pest control research, etc.), and no longer publishes book reviews or editorials. Insecta Mundi publishes original research or discoveries in an inexpensive and timely manner, distributing them free via open access on the internet on the date of publication. Insecta Mundi is referenced or abstracted by several sources including the Zoological Record, CAB Ab- stracts, etc. Insecta Mundi is published irregularly throughout the year, with completed manuscripts assigned an individual number. Manuscripts must be peer reviewed prior to submission, after which they are reviewed by the editorial board to ensure quality. -
(LINNAEUS, 1758) in the SOUTH of WESTERN SIBERIA, RUSSIA (CHILOPODA: SCUTIGEROMORPHA: SCUTIGERIDAE) 1Altai State University, Lenina Avenue, 61, Barnaul 656049, Russia
428 Бiологiчний вiсник UDC 595.624 Nefediev P.S.1, Tuf I.H.2, Dyachkov Yu.V.1, Efimov D.A.3 FIRST RECORD OF SCUTIGERA COLEOPTRATA (LINNAEUS, 1758) IN THE SOUTH OF WESTERN SIBERIA, RUSSIA (CHILOPODA: SCUTIGEROMORPHA: SCUTIGERIDAE) 1Altai State University, Lenina Avenue, 61, Barnaul 656049, Russia. E-mail: [email protected] 2Palacký University, Šlechtitelů 27, Olomouc 77900, Czech Republic. E-mail: [email protected] 3Kemerovo State University, Krasnaya Street, 6, Kemerovo 650043, Russia. E-mail: [email protected] The order, family, genus and species of the house centipede are new to Asian Russia’s list: Scutigeromorpha, Scutigeridae, Scutigera Lamark, 1801, and Scutigera coleoptrata (Linnaeus, 1758). All records of the species in the south of western Siberia appear to be associated with synanthropic habitats. Distributional remarks are provided, all currently reported findings being mapped as well. Key words: house centipede, Scutigera coleoptrata, Scutigeridae, Scutigeromorpha, anthropochore, faunistics, introduction, Siberia. INTRODUCTION The centipede fauna of Siberia is very poorly-studied. All former research has been devoted to Lithobiomorpha and Geophilomorpha in natural habitats. Investigating anthropogenic habitats in the south of western Siberia, we have currently found the house centipede Scutigera coleoptrata (Linnaeus, 1758). Both the order Scutigeromorpha, and the family Scutigeridae it belongs to, are almost worldwide, distributed in all continents, on all major islands and many oceanic islands with the exception of Antarctica, and many records refer to introduced populations of Scutigera coleoptrata (Bonato & Zapparoli, 2011). The samples treated below have been deposited in the collection of the Altai State University, Barnaul, Russia (ASU). RESULTS SCUTIGEROMORPHA Pocock, 1895 SCUTIGERIDAE Gervais, 1837 Scutigera coleoptrata (Linnaeus, 1758) ISSN 2225-5486 (Print), ISSN 2226-9010 (Online). -
On the Presence of Scutigera Coleoptrata (Linnaeus, 1758) (Chilopoda: Scutigeromorpha: Scutigeridae) in the Metropolitan Region, Chile
MASUMOTO, K., G. DELLACASA & M. KIUCHI 1990. On the Aphodius de Storia naturale, Milano, 114: 51-70. ● REITTER, E. 1895. Einige species of Japan. Entomological Review of Japan, 45: 145-156. ● neue Coleopteren aus Korea und China. Wiener entomologische MÜLLER, G. 1941. Nuovi Coleotteri dell’Africa Orientale. Atti del Zeitung, 14: 208-210. ● SCHMIDT, A. 1907. Zusammentellung der Museo civico di Storia naturale di Trieste, 14: 319-352. ● NEAVE, bis 1906 beschriebenen Aphodiinen. Deutsche entomologische S.A. 1939. Nomenclator Zoologicus. A List of the Names of Genera Zeitschrift, Beilage, 1907-1908: 1-141. ● SCHMIDT, A. 1910a. Col- and Subgenera in Zoology from the Tenth Edition of Linnaeus 1758 eoptera Lamellicornia, Fam. Aphodiidae. 110me Fascicule. In: P. to the End of 1935. Vol. 1, A-C. The Zoological Society of London, Wytsman (ed.), Genera Insectorum. Tervueren, 155 pp, 3 pls. ● London, xiv + 957 pp. ● PAULIAN, R. 1942. Exploration du Parc SCHMIDT, A. 1910b. Aphodiinae. Pars 20, Vol. 19(4). In: S. Schenk- National Albert. Mission G. F. de Witte (1933-35). Fasc. 35. Aphodi- ling (ed.), Coleopterorum Catalogus. W. Junk, Berlin, 111 pp. ● inae (Coleoptera Lamellicornia) Fam. Scarabaeidae. Institut des SCHMIDT, A. 1913. Erster Versuch einer Einteilung der exotischen Parcs Nationaux du Congo Belge, 143 pp., 23 pls. ● PETROVITZ, R. Aphodien in Subgenera und als Anhang einige Neubeschreibungen. 1958. Neue afrikanischen Aphodiusarten (Col. Scarab.). Entomolo- Archiv für Naturgeschichte. Abtheilung A, Original-Arbeiten, 79: 117- gische Arbeiten aus dem Museum G. Frey, 9: 140-159. ● 178. ● SCHMIDT, A. 1922. Coleoptera, Aphodiinae. In: C. Apstein PETROVITZ, R. 1962. Neue und verkannte Aphodiinae aus allen (ed.), Das Tierreich. -
Chilopoda; Scolopendridae
Bijdragen tot dl Dierkunde, 55 (1): 125-130 — 1985 Possible species isolation mechanisms in some scolopendrid centipedes (Chilopoda; Scolopendridae) by J.G.E. Lewis Taunton School, Taunton, Somerset TA2 6AD, England the femur of Abstract are seen on Eupolybothrus spp. Various other lithobiid secondary sexual sexual characters in dis- Secondary centipedes are briefly characters have been reviewed by Lewis (1981). cussed and it is that the the suggested spines on prefemora of the described Differences type above are of the last pair of legs in some scolopendrids are used in presumably associated with mating behaviour specific discrimination prior to mating. The hypothesis is in which male and female head discussed with reference of the come together to Scolopendra spp. eastern Mediterranean,north-east Africa and Arabia. to tail, and the antennae and the last pair of legs Where species of Scolopendra with identical The virtually are tapped. morphological adaptations in spinulation on the last legs are sympatric, a large size dif- the males would serve for the femalesto identify ference exists between them. different and sex. It is that in where the species suggested some genera prefemoral have been inhibited. In spines are absent, speciation may the where be absent genus Otostigmus spines may or spine similar in number of other patterns are very a species DIMORPHISM IN SCOLOPENDRIDAE secondary sexual characters have developed. Sexual is also in dimorphism seen the scolopen- INTRODUCTION dromorph family Scolopendridae. In Scolopendra morsitans Linnaeus the dorsal side of the Centipedes not infrequently exhibit secondary prefemur, femur and sometimes the tibiaof the last of is sexual characters. -
Evolution of Centipede Venoms Under Morphological Constraint
Production and packaging of a biological arsenal: Evolution of centipede venoms under morphological constraint Eivind A. B. Undheima,b, Brett R. Hamiltonc,d, Nyoman D. Kurniawanb, Greg Bowlayc, Bronwen W. Cribbe, David J. Merritte, Bryan G. Frye, Glenn F. Kinga,1, and Deon J. Venterc,d,f,1 aInstitute for Molecular Bioscience, bCentre for Advanced Imaging, eSchool of Biological Sciences, fSchool of Medicine, and dMater Research Institute, University of Queensland, St. Lucia, QLD 4072, Australia; and cPathology Department, Mater Health Services, South Brisbane, QLD 4101, Australia Edited by Jerrold Meinwald, Cornell University, Ithaca, NY, and approved February 18, 2015 (received for review December 16, 2014) Venom represents one of the most extreme manifestations of (11). Similarly, the evolution of prey constriction in snakes has a chemical arms race. Venoms are complex biochemical arsenals, led to a reduction in, or secondary loss of, venom systems despite often containing hundreds to thousands of unique protein toxins. these species still feeding on formidable prey (12–15). However, Despite their utility for prey capture, venoms are energetically in centipedes (Chilopoda), which represent one of the oldest yet expensive commodities, and consequently it is hypothesized that least-studied venomous lineages on the planet, this inverse re- venom complexity is inversely related to the capacity of a venom- lationship between venom complexity and physical subdual of ous animal to physically subdue prey. Centipedes, one of the prey appears to be absent. oldest yet least-studied venomous lineages, appear to defy this There are ∼3,300 extant centipede species, divided across rule. Although scutigeromorph centipedes produce less complex five orders (16). -
Crocodylus Moreletii
ANFIBIOS Y REPTILES: DIVERSIDAD E HISTORIA NATURAL VOLUMEN 03 NÚMERO 02 NOVIEMBRE 2020 ISSN: 2594-2158 Es un publicación de la CONSEJO DIRECTIVO 2019-2021 COMITÉ EDITORIAL Presidente Editor-en-Jefe Dr. Hibraim Adán Pérez Mendoza Dra. Leticia M. Ochoa Ochoa Universidad Nacional Autónoma de México Senior Editors Vicepresidente Dr. Marcio Martins (Artigos em português) Dr. Óscar A. Flores Villela Dr. Sean M. Rovito (English papers) Universidad Nacional Autónoma de México Editores asociados Secretario Dr. Uri Omar García Vázquez Dra. Ana Bertha Gatica Colima Dr. Armando H. Escobedo-Galván Universidad Autónoma de Ciudad Juárez Dr. Oscar A. Flores Villela Dra. Irene Goyenechea Mayer Goyenechea Tesorero Dr. Rafael Lara Rezéndiz Dra. Anny Peralta García Dr. Norberto Martínez Méndez Conservación de Fauna del Noroeste Dra. Nancy R. Mejía Domínguez Dr. Jorge E. Morales Mavil Vocal Norte Dr. Hibraim A. Pérez Mendoza Dr. Juan Miguel Borja Jiménez Dr. Jacobo Reyes Velasco Universidad Juárez del Estado de Durango Dr. César A. Ríos Muñoz Dr. Marco A. Suárez Atilano Vocal Centro Dra. Ireri Suazo Ortuño M. en C. Ricardo Figueroa Huitrón Dr. Julián Velasco Vinasco Universidad Nacional Autónoma de México M. en C. Marco Antonio López Luna Dr. Adrián García Rodríguez Vocal Sur M. en C. Marco Antonio López Luna Universidad Juárez Autónoma de Tabasco English style corrector PhD candidate Brett Butler Diseño editorial Lic. Andrea Vargas Fernández M. en A. Rafael de Villa Magallón http://herpetologia.fciencias.unam.mx/index.php/revista NOTAS CIENTÍFICAS SKIN TEXTURE CHANGE IN DIASPORUS HYLAEFORMIS (ANURA: ELEUTHERODACTYLIDAE) ..................... 95 CONTENIDO Juan G. Abarca-Alvarado NOTES OF DIET IN HIGHLAND SNAKES RHADINAEA EDITORIAL CALLIGASTER AND RHADINELLA GODMANI (SQUAMATA:DIPSADIDAE) FROM COSTA RICA ..... -
Arxiv:2104.01203V2 [Physics.Bio-Ph] 24 Apr 2021
Universal features in panarthropod inter-limb coordination during forward walking Jasmine A. Nirody1,2 1Center for Studies in Physics and Biology, Rockefeller University, New York, NY 10065 USA 2All Souls College, University of Oxford, Oxford OX1 4AL United Kingdom April 27, 2021 Abstract Terrestrial animals must often negotiate heterogeneous, varying environments. Accordingly, their locomotive strategies must adapt to a wide range of terrain, as well as to a range of speeds in order to accomplish different behavioral goals. Studies in Drosophila have found that inter-leg coordination patterns (ICPs) vary smoothly with walking speed, rather than switching between distinct gaits as in vertebrates (e.g., horses transitioning between trotting and galloping). Such a continuum of stepping patterns implies that separate neural controllers are not necessary for each observed ICP. Furthermore, the spectrum of Drosophila stepping patterns includes all canonical coordination patterns observed during forward walking in insects. This raises the exciting possibility that the controller in Drosophila is common to all insects, and perhaps more generally to panarthropod walkers. Here, we survey and collate data on leg kinematics and inter-leg coordination relationships during forward walking in a range of arthropod species, as well as include data from a recent behavioral investigation into the tardigrade Hypsibius exemplaris. Using this comparative dataset, we point to several functional and morphological features that are shared amongst panarthropods. The goal of the framework presented in this review is to emphasize the importance of comparative functional and morphological analyses in understanding the origins and diversification of walking in Panarthropoda. Walking, a behavior fundamental to numerous tasks important for an organism's survival, is assumed to have become highly optimized during evolution. -
Arachnides 76
Arachnides, 2015, n°76 ARACHNIDES BULLETIN DE TERRARIOPHILIE ET DE RECHERCHES DE L’A.P.C.I. (Association Pour la Connaissance des Invertébrés) 76 2015 0 Arachnides, 2015, n°76 LES PREDATEURS DES SCORPIONS (ARACHNIDA : SCORPIONES) G. DUPRE Dans leur revue sur les prédateurs de scorpions, Polis, Sissom & Mac Cormick (1981) relèvent 150 espèces dont essentiellement des espèces adaptées au comportement nocturne de leur proie (chouettes, rongeurs, carnivores nocturnes) mais également des espèces diurnes (lézards, rongeurs, carnivores....) qui débusquent les scorpions sous les pierres ou dans leurs terriers. Dans une précédente note (Dupré, 2008) nous avions effectué un relevé afin d'actualiser cette étude de 1981. Sept ans après, de nouvelles données sont présentées dans cette synthèse. Voici un nouveau relevé des espèces prédatrices. Nous ne faisons pas mention des scorpions qui feront l'objet d'un futur article traité avec le cannibalisme. Explication des tableaux: La première colonne correspond aux prédateurs, la seconde aux régions concernées et la troisième aux références. Dans la mesure du possible, les noms scientifiques ont été rectifiés en fonction des synonymies ou des nouvelles combinaisons appliquées depuis les dates de publication d'origine. ARTHROPODA ARACHNIDA SOLIFUGAE Solifugae Afrique du Nord Millot & Vachon, 1949; Punzo, 1998; Cloudsley-Thompson, 1977 Eremobates sp. USA Bradley, 1983 ARACHNIDA ARANEAE Acanthoscurria atrox Brésil Lourenço, 1981 Aphonopelma sp. et autres Amérique centrale Mazzotti, 1964 Teraphosidae Phormictopus auratus Cuba Teruel & De Armas, 2012 Brachypelma vagans Mexique Dor et al., 2011 Epicadus heterogaster Brésil Lourenço et al. 2006 Latrodectus sp. USA Baerg, 1961 L. hesperus USA Polis et al., 1981 L. mactans Cuba Teruel, 1996; Teruel & De Armas, 2012 L. -
A New Scolopendromorph Centipede from Belize
SOIL ORGANISMS Volume 81 (3) 2009 pp. 519–530 ISSN: 1864 - 6417 Ectonocryptoides sandrops – a new scolopendromorph centipede from Belize Arkady A. Schileyko Zoological Museum of Moscow State Lomonosov University, Bolshaja Nikitskaja Str.6, 103009, Moscow, Russia; e-mail: [email protected] Abs tract A new representative of the rare subfamily Ectonocryptopinae (Scolopocryptopidae) is described from western Belize as Ectonocryptoides sandrops sp. nov. Both previously known representatives of this subfamily ( Ectonocryptops kraepelini Crabill, 1977 and Ectonocryptiodes quadrimeropus Shelley & Mercurio, 2005) and the new species have been compared and the taxonomic status of the latter has been analysed. Keywords: Ectonocryptopinae, new species, Belize 1. Introduction Some years ago, working on exotic Scolopendromorpha from a collection of Prof. Alessandro Minelli I found one very small (ca 11–12 mm long) scolopendromorph centipede (Fig. 1). It had been collected by Francesco Barbieri in Mountain Pine Ridge of Western Belize (Fig. 2). With 23 pedal segments this blind centipede clearly belongs to the family Scolopocryptopidae Pocock, 1896. According to the very special structure of the terminal legs I have identified this animal as a new species of the very rare subfamily Ectonocryptopinae Shelley & Mercurio, 2005. The structure of the terminal legs (= legs of the ultimate body segment) is of considerable taxonomic importance in the order Scolopendromorpha. Commonly the terminal leg consists of 5 podomeres (prefemur, femur, tibia, tarsus 1, tarsus 2) and pretarsus. The first four podomeres are always present, when tarsus 2 and the pretarsus may both be absent. The terminal podomeres are the most transformable ones. There are six principle (or basic) types of terminal legs among scolopendromorph centipedes: 1) ‘common’ shape (the most similar to the locomotory legs), which is the least specialised (Fig. -
Chilopoda: Scolopendromorpha: Cryptopidae) in Belarus
Arthropoda Selecta 27(1): 31–32 © ARTHROPODA SELECTA, 2018 The first record of Cryptops hortensis (Donovan, 1810) (Chilopoda: Scolopendromorpha: Cryptopidae) in Belarus Ïåðâàÿ íàõîäêà Cryptops hortensis (Donovan, 1810) (Chilopoda: Scolopendromorpha: Cryptopidae) â Áåëàðóñè A.M. Ostrovsky À.Ì. Îñòðîâñêèé Gomel State Medical University, Lange str. 5, Gomel 246000 Republic of Belarus. E-mail: [email protected] Гомельский государственный медицинский университет, ул. Ланге 5, Гомель 246000 Республика Беларусь. KEY WORDS: Cryptops hortensis, faunistics, synathropy, Belarus. КЛЮЧЕВЫЕ СЛОВА: Cryptops hortensis, фаунистика, синантропия, Беларусь. ABSTRACT. The centipede Cryptops hortensis among household waste, 24.09.2016, all leg. et det. A.M. Ostro- (Donovan, 1810) from the family Cryptopidae, found in vsky. the city of Gomel in autumn 2016, is new to the fauna of Four of the above samples have been deposited in the Belarus. The record is clearly synathropic. Data on the author’s collection, but one specimen has been donated to global distribution of the species are presented. the collection of the Zoological Museum of the Moscow State University. How to cite this article: Ostrovsky A.M. 2018. The DISTRIBUTION. Being Central Asian-European in ori- first record of Cryptops hortensis (Donovan, 1810) gin, the cryptopid scolopendromorph C. hortensis is wide- (Chilopoda: Scolopendromorpha: Cryptopidae) in Be- spread across most of Europe, currently known from Alba- larus // Arthropoda Selecta. Vol.27. No.1. P.31–32. nia, Austria, Belgium, Bosnia and Hercegovina, Bulgaria, doi: 10.15298/arthsel. 27.1.03 Croatia, Czech Republic, Denmark, mainland and insular Greece including Crete and the Dodecanese islands, Great РЕЗЮМЕ. Многоножка Cryptops hortensis (Do- Britain including the Channel Islands and Northern Ireland, novan, 1810) из семейства Cryptopidae, найденная в Finland, mainland France including Corsica, Germany, Hun- городе Гомель осенью 2016 г., новый для фауны gary, Ireland, mainland Italy as well as Sicily and Sardinia, Беларуси. -
Biodiversity from Caves and Other Subterranean Habitats of Georgia, USA
Kirk S. Zigler, Matthew L. Niemiller, Charles D.R. Stephen, Breanne N. Ayala, Marc A. Milne, Nicholas S. Gladstone, Annette S. Engel, John B. Jensen, Carlos D. Camp, James C. Ozier, and Alan Cressler. Biodiversity from caves and other subterranean habitats of Georgia, USA. Journal of Cave and Karst Studies, v. 82, no. 2, p. 125-167. DOI:10.4311/2019LSC0125 BIODIVERSITY FROM CAVES AND OTHER SUBTERRANEAN HABITATS OF GEORGIA, USA Kirk S. Zigler1C, Matthew L. Niemiller2, Charles D.R. Stephen3, Breanne N. Ayala1, Marc A. Milne4, Nicholas S. Gladstone5, Annette S. Engel6, John B. Jensen7, Carlos D. Camp8, James C. Ozier9, and Alan Cressler10 Abstract We provide an annotated checklist of species recorded from caves and other subterranean habitats in the state of Georgia, USA. We report 281 species (228 invertebrates and 53 vertebrates), including 51 troglobionts (cave-obligate species), from more than 150 sites (caves, springs, and wells). Endemism is high; of the troglobionts, 17 (33 % of those known from the state) are endemic to Georgia and seven (14 %) are known from a single cave. We identified three biogeographic clusters of troglobionts. Two clusters are located in the northwestern part of the state, west of Lookout Mountain in Lookout Valley and east of Lookout Mountain in the Valley and Ridge. In addition, there is a group of tro- globionts found only in the southwestern corner of the state and associated with the Upper Floridan Aquifer. At least two dozen potentially undescribed species have been collected from caves; clarifying the taxonomic status of these organisms would improve our understanding of cave biodiversity in the state.