Cockroaches (Ectobius Vittiventris)
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The Dusky Cockroach in the Canadian Maritimes: Establishment, Persistence, and Ecology Jeff C
J. Acad. Entomol. Soc. 13: 21-27 (2017) The Dusky Cockroach in the Canadian Maritimes: establishment, persistence, and ecology Jeff C. Clements, David B. McCorquodale, Denis A. Doucet, Jeffrey B. Ogden ABSTRACT The Dusky Cockroach, Ectobius lapponicus (Linnaeus, 1758) (Blattodea: Blatellidae), a European native, is an introduced species in North America that was first discovered in New Hampshire in 1984. In Canada, this species was first found in Prince Edward Island in 1991 and has recently been recorded in all three Maritime Provinces. Using ad libitum reports of Ectobius lapponicus sightings with confirmed species identification, we provide an update for an earlier postulation of the establishment and persistence of this non-native cockroach in the Canadian Maritimes, highlighting spatial and temporal trends in Ectobius lapponicus records. While a 13-year gap exists after its original Canadian record in 1991, Ectobius lapponicus has been observed in the Maritimes almost annually since 2004. To date, a total of 119 Ectobius lapponicus individuals have been reported in the Canadian Maritimes: 45 from New Brunswick, 38 from Nova Scotia, and 36 from Prince Edward Island. Seventy-eight percent of individuals are reported from tourist destinations (parks and campgrounds). The vast majority of individuals have been observed outdoors in disturbed habitats near forest edges, although some indoor records exist. Records suggest that this species is active from June–September, which is in accordance with typical periods of activity in Europe. This species also appears well established in Ontario. Widespread confirmation of this species throughout the state of Maine supports the northward spread of this species from New Hampshire into the Canadian Maritimes, likely driven by human-assisted dispersal. -
A Dichotomous Key for the Identification of the Cockroach Fauna (Insecta: Blattaria) of Florida
Species Identification - Cockroaches of Florida 1 A Dichotomous Key for the Identification of the Cockroach fauna (Insecta: Blattaria) of Florida Insect Classification Exercise Department of Entomology and Nematology University of Florida, Gainesville 32611 Abstract: Students used available literature and specimens to produce a dichotomous key to species of cockroaches recorded from Florida. This exercise introduced students to techniques used in studying a group of insects, in this case Blattaria, to produce a regional species key. Producing a guide to a group of insects as a class exercise has proven useful both as a teaching tool and as a method to generate information for the public. Key Words: Blattaria, Florida, Blatta, Eurycotis, Periplaneta, Arenivaga, Compsodes, Holocompsa, Myrmecoblatta, Blatella, Cariblatta, Chorisoneura, Euthlastoblatta, Ischnoptera,Latiblatta, Neoblatella, Parcoblatta, Plectoptera, Supella, Symploce,Blaberus, Epilampra, Hemiblabera, Nauphoeta, Panchlora, Phoetalia, Pycnoscelis, Rhyparobia, distributions, systematics, education, teaching, techniques. Identification of cockroaches is limited here to adults. A major source of confusion is the recogni- tion of adults from nymphs (Figs. 1, 2). There are subjective differences, as well as morphological differences. Immature cockroaches are known as nymphs. Nymphs closely resemble adults except nymphs are generally smaller and lack wings and genital openings or copulatory appendages at the tip of their abdomen. Many species, however, have wingless adult females. Nymphs of these may be recognized by their shorter, relatively broad cerci and lack of external genitalia. Male cockroaches possess styli in addition to paired cerci. Styli arise from the subgenital plate and are generally con- spicuous, but may also be reduced in some species. Styli are absent in adult females and nymphs. -
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. -
Florida Blattodea (Cockroaches)
Species Identification - Insects of Florida 1 A Literature-based Dichotomous Key for the Identification of the Cockroach fauna (Insecta: Blattodea) of Florida Insect Classification Exercise Department of Entomology and Nematology University of Florida, Gainesville 32611 Abstract: Students used available literature and specimens to produce a dichotomous key to species of cockroaches recorded from Florida. This exercise introduced students to techniques used in studying a group of insects, in this case Blattodea, to produce a regional species key. Producing a guide to a group of insects as a class exercise has proven useful both as a teaching tool and as a method to generate information for the public. Key Words: Blattodea, Florida, Blatta, Eurycotis, Periplaneta, Arenivaga, Compsodes, Holocompsa, Myrmecoblatta, Blattella, Cariblatta, Chorisoneura, Euthlastoblatta, Ischnoptera,Latiblatta, Neoblattella, Parcoblatta, Plectoptera, Supella, Symploce,Blaberus, Epilampra, Hemiblabera, Nauphoeta, Panchlora, Phoetalia, Pycnoscelis, Rhyparobia, distributions, systematics, education, teaching, techniques. Identification of cockroaches is limited here to adults. A major source of confusion is the recogni- tion of adults from nymphs (Figs. 1, 2). There are subjective differences, as well as morphological differences. Immature cockroaches are known as nymphs. Nymphs closely resemble adults except nymphs are generally smaller and lack wings and genital openings or copulatory appendages at the tip of their abdomen. Many species, however, have wingless adult females. Nymphs of these may be recognized by their shorter, relatively broad cerci and lack of external genitalia. Male cockroaches possess styli in addition to paired cerci. Styli arise from the subgenital plate and are generally con- spicuous, but may also be reduced in some species. Styli are absent in adult females and nymphs. -
Phylogeny and Life History Evolution of Blaberoidea (Blattodea)
78 (1): 29 – 67 2020 © Senckenberg Gesellschaft für Naturforschung, 2020. Phylogeny and life history evolution of Blaberoidea (Blattodea) Marie Djernæs *, 1, 2, Zuzana K otyková Varadínov á 3, 4, Michael K otyk 3, Ute Eulitz 5, Kla us-Dieter Klass 5 1 Department of Life Sciences, Natural History Museum, London SW7 5BD, United Kingdom — 2 Natural History Museum Aarhus, Wilhelm Meyers Allé 10, 8000 Aarhus C, Denmark; Marie Djernæs * [[email protected]] — 3 Department of Zoology, Faculty of Sci- ence, Charles University, Prague, 12844, Czech Republic; Zuzana Kotyková Varadínová [[email protected]]; Michael Kotyk [[email protected]] — 4 Department of Zoology, National Museum, Prague, 11579, Czech Republic — 5 Senckenberg Natural History Collections Dresden, Königsbrücker Landstrasse 159, 01109 Dresden, Germany; Klaus-Dieter Klass [[email protected]] — * Corresponding author Accepted on February 19, 2020. Published online at www.senckenberg.de/arthropod-systematics on May 26, 2020. Editor in charge: Gavin Svenson Abstract. Blaberoidea, comprised of Ectobiidae and Blaberidae, is the most speciose cockroach clade and exhibits immense variation in life history strategies. We analysed the phylogeny of Blaberoidea using four mitochondrial and three nuclear genes from 99 blaberoid taxa. Blaberoidea (excl. Anaplectidae) and Blaberidae were recovered as monophyletic, but Ectobiidae was not; Attaphilinae is deeply subordinate in Blattellinae and herein abandoned. Our results, together with those from other recent phylogenetic studies, show that the structuring of Blaberoidea in Blaberidae, Pseudophyllodromiidae stat. rev., Ectobiidae stat. rev., Blattellidae stat. rev., and Nyctiboridae stat. rev. (with “ectobiid” subfamilies raised to family rank) represents a sound basis for further development of Blaberoidea systematics. -
The New Genus Planuncus and Its Relatives (Insecta: Blattodea: Ectobiinae) 139-168 71 (3): 139 – 168 20.12.2013
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Arthropod Systematics and Phylogeny Jahr/Year: 2013 Band/Volume: 71 Autor(en)/Author(s): Bohn Horst, Beccaloni George, Dorow Wolfgang H. O., Pfeifer Manfred Alban Artikel/Article: Another species of European Ectobiinae travelling north – the new genus Planuncus and its relatives (Insecta: Blattodea: Ectobiinae) 139-168 71 (3): 139 – 168 20.12.2013 © Senckenberg Gesellschaft für Naturforschung, 2013. Another species of European Ectobiinae travelling north – the new genus Planuncus and its relatives (Insecta: Blattodea: Ectobiinae) Horst Bohn *, 1, George Beccaloni 2, Wolfgang H.O. Dorow 3 & Manfred Alban Pfeifer 4 1 Zoologische Staatssammlung München, Münchhausenstrasse 21, 81247 München, Germany; Horst Bohn * [[email protected] chen.de] — 2 The Natural History Museum, London SW7 5BD, UK; George Beccaloni [[email protected]] — 3 Senckenberg For- schungsinstitut und Naturmuseum, Senckenberganlage 25, 60325 Frankfurt am Main, Germany; Wolfgang Dorow [Wolfgang.Dorow@ sen ckenberg.de] — 4 Bahnhofsplatz 5, 67240 Bobenheim-Roxheim, Germany; Manfred Alban Pfeifer [[email protected]] — * Corresponding author Accepted 21.xi.2013. Published online at www.senckenberg.de/arthropod-systematics on 13.xii.2013. Abstract A new genus of Ectobiinae is described, Planuncus with the three new subgenera, Planuncus, Margundatus and Margintorus, containing species formerly belonging to the genera Phyllodromica (second subg.) and Ectobius (other subg.). New combinations: Pl. (Pl.) tingitanus (Bolívar, 1914), Pl. (Pl.) finoti (Chopard, 1943), Pl. (Pl.) vinzi (Maurel, 2012); Pl. (Margundatus) baeticus (Bolívar, 1884), Pl. (Margun- datus) agenjoi (Harz, 1971), Pl. (Margundatus) erythrurus (Bohn, 1992), Pl. (Margundatus) intermedius (Bohn, 1992), Pl. -
Fossil Calibrations for the Cockroach Phylogeny (Insecta, Dictyoptera, Blattodea)
Palaeontologia Electronica palaeo-electronica.org Fossil calibrations for the cockroach phylogeny (Insecta, Dictyoptera, Blattodea), comments on the use of wings for their identification, and a redescription of the oldest Blaberidae Dominic A. Evangelista, Marie Djernæs, and Manpreet Kaur Kohli ABSTRACT Here we provide the first thorough assessment of the fossil calibrations for diver- gence time estimation of cockroaches. Through a review of published fossil descrip- tions, we evaluate oldest fossils for various nodes in crown Blattodea in accordance with recently proposed best practices. Since most descriptions of fossil cockroaches rely heavily on wing and tegminal venation, we also provide a critical assessment of Rehn (1951), which is the most extensive work on these characters. We find that Rehn (1951) incorrectly reported the state of numerous characters. This, combined with the low number of informative characters in cockroach wings, negatively affects phyloge- netic justifications of some of the oldest purported fossil cockroaches. We conclude that currently the best fossils to use for calibration of the cockroach tree are: Cretahol- ocompsa montsecana, “Gyna” obesa, Cariblattoides labandeirai, and Ectobius kohlsi. One of these, “Gyna” obesa, was insufficiently treated in its original description, so we provide a redescription facilitated by high resolution imagery and modern systematic knowledge. We comment on the difficulty of utilizing the so-called fossil roachoids because their position at the base of Dictyoptera is under dispute and cannot be reli- ably verified. We do not include calibrations for termite lineages. Dominic A. Evangelista, Muséum National d'Histoire Naturelle, 45 Rue Buffon CP50, Paris, France 75005. [email protected] Marie Djernæs. -
Comparative Morphological Studies of Proventriculi in the Order
This dissertation has been 69-15,943 microfilmed exactly as received MILLER, Henry Keith, 1934- COMPARATIVE MORPHOLOGICAL STUDIES OF PROV ENTRICULI IN THE ORDER DICTYOPTERA: SUBORDER BLATTARIA. The Ohio State University, PiuD., 1969 Entomology University Microfilms, Inc., Ann Arbor, Michigan COMPAR ATIVE MORPHOLOGICAL STUDIES OF PROVENTRICULI IN THE ORDER DICTYOPTERA: SUBORDER BLA TTA RIA DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Henry Keith Miller, B. S. in Educ. , M. S. Ent. s{s sje sjc $ 9jc # The Ohio State University 1969 Approved by A d v ise r Faculty of Entomology ACKNOWLEDGMENTS My sincere thanks go to Dr. Frank W. Fisk for his in valuable advice and encouragement during the course of this investigation, as well as the generous contribution of specimens from his personal collection. I would also like to express my deep appreciation for the numerous specimens contributed by the following persons: Dr. Louis M. Roth, Pioneering Research Laboratory, U. S. Army Natick Laboratories, Natick, Massachusetts; Dr. M. J. Mackerras, Division of Entomology, Australian Commonwealth Scientific and Industrial Research Organization; Dr. Ashley B. Gurney, National Museum, Washington, D. C. ; and Dr. Charles A. Triplehorn, Curator of Insects, The Ohio State University. Photographic illustrations herein were made possible by the generous cooperation of Dr. Paul A. Colinvaux, Faculty of Popula tion and Environmental Biology, The Ohio State University, who permitted the use of sophisticated photomicrography equipment. Technical advice was generously contributed by Dr. Colinvaux, Dr. Eileen K. Schofield, The Ohio State University, as well as Harold "Bo" Hagen, regional representative of Leitz, Inc. -
Sunninghill, ASCOT, Berkshire
Aspects of the biology and growth of three species of Ectobius (Dictyoptera: Blattidae). by Valerie Kathleen BROWN, B.Sc.(Lond.), A.R.C.S. Thesis submitted for the Degree of Doctor of Philosophy November 1969 Imperial College of Science and Technology, Silwood Park, Sunninghill, ASCOT, Berkshire. -1- ABSTRACT This thesis concerns three species in the genus Ectobius Stephens which occur in Britain. The basic life histories of the species are clarified and several biological topics are considered in more detail. Aspects of the oviposition behaviour in mated and unmated females and the extent of parthenogenesis in the species are investigated. The oothecae pass the winter in a state of dormancy which has been confirmed as a diapause in Ectobiuslayponicus. (Linnaeus). Oothecae are subject to attack by the Evaniid parasite, Brachygaster minutus (Olivier); the life history of this species is considered in relation to that of the host. The overwintering behaviour of the nymphal instars of E. lapponicus and Ectobius 1,allidus (Olivier) in a range of intermediate instars has been found to involve a diapause in the former species. The relationship between the proportion of nymphs entering the winter in each instar and the nature of the adult emergence the following summer is discussed. The post-embryonic growth of two species with different life cycles, E. lapponicus and Ectobius panzeri Stephens, is considered mainly from an analytical standpoint. A means of determining the sex of the nymphal instars is described and thus permits a more detailed study. The post-embryonic development is analysed by several techniques, each of which is applied to a large number of characters. -
The Arthropod Fauna of Oak (Quercus Spp., Fagaceae) Canopies in Norway
diversity Article The Arthropod Fauna of Oak (Quercus spp., Fagaceae) Canopies in Norway Karl H. Thunes 1,*, Geir E. E. Søli 2, Csaba Thuróczy 3, Arne Fjellberg 4, Stefan Olberg 5, Steffen Roth 6, Carl-C. Coulianos 7, R. Henry L. Disney 8, Josef Starý 9, G. (Bert) Vierbergen 10, Terje Jonassen 11, Johannes Anonby 12, Arne Köhler 13, Frank Menzel 13 , Ryszard Szadziewski 14, Elisabeth Stur 15 , Wolfgang Adaschkiewitz 16, Kjell M. Olsen 5, Torstein Kvamme 1, Anders Endrestøl 17, Sigitas Podenas 18, Sverre Kobro 1, Lars O. Hansen 2, Gunnar M. Kvifte 19, Jean-Paul Haenni 20 and Louis Boumans 2 1 Norwegian Institute of Bioeconomy Research (NIBIO), Department Invertebrate Pests and Weeds in Forestry, Agriculture and Horticulture, P.O. Box 115, NO-1431 Ås, Norway; [email protected] (T.K.); [email protected] (S.K.) 2 Natural History Museum, University of Oslo, P.O. Box 1172 Blindern, NO-0318 Oslo, Norway; [email protected] (G.E.E.S.); [email protected] (L.O.H.); [email protected] (L.B.) 3 Malomarok, u. 27, HU-9730 Köszeg, Hungary; [email protected] 4 Mågerøveien 168, NO-3145 Tjøme, Norway; [email protected] 5 Biofokus, Gaustadalléen 21, NO-0349 Oslo, Norway; [email protected] (S.O.); [email protected] (K.M.O.) 6 University Museum of Bergen, P.O. Box 7800, NO-5020 Bergen, Norway; [email protected] 7 Kummelnäsvägen 90, SE-132 37 Saltsjö-Boo, Sweden; [email protected] 8 Department of Zoology, University of Cambridge, Downing St., Cambridge CB2 3EJ, UK; [email protected] 9 Institute of Soil Biology, Academy of Sciences of the Czech Republic, Na Sádkách 7, CZ-37005 Ceskˇ é Budˇejovice,Czech Republic; [email protected] Citation: Thunes, K.H.; Søli, G.E.E.; 10 Netherlands Food and Consumer Product Authority, P.O. -
Abundance and Distribution of the Forest Cockroaches in Different Algerian Ecosystems
Journal of Bioresource Management Volume 8 Issue 3 Article 7 Abundance and Distribution of the Forest Cockroaches in Different Algerian Ecosystems Zakaria Hedjouli Applied Neuroendocrinology Laboratory, Department of Biology, Faculty of Sciences, University of Badji Mokhtar, Annaba, Algeria, [email protected] Wafa Habbachi Applied Neuroendocrinology Laboratory, Department of Biology, Faculty of Sciences, University of Badji Mokhtar, Annaba, Algeria., [email protected] Fatiha Masna Department of Natural Sciences, Ens Taleb Ebderrahman, Laghouat, Algeria, [email protected] Saliha Benhissen Department of Natural and Life Sciences, Faculty of Sciences, University of Mohamed Boudiaf, M'sila, Algeria., [email protected] Sarra Habbachi Applied Neuroendocrinology Laboratory, Department of Biology, Faculty of Sciences, University of Badji Mokhtar, Annaba, Algeria, [email protected] See next page for additional authors Follow this and additional works at: https://corescholar.libraries.wright.edu/jbm Part of the Forest Biology Commons, and the Zoology Commons Recommended Citation Hedjouli, Z., Habbachi, W., Masna, F., Benhissen, S., Habbachi, S., Asloum, A., & Tahraoui, A. (2021). Abundance and Distribution of the Forest Cockroaches in Different Algerian Ecosystems, Journal of Bioresource Management, 8 (3). DOI: https://doi.org/10.35691/JBM.1202.0196 ISSN: 2309-3854 online (Received: Apr 10, 2021; Accepted: Apr 29, 2021; Published: Aug 26, 2021) This Article is brought to you for free and open access by CORE Scholar. -
Latiblattella Avita Sp. Nov. (Blattaria: Ectobiidae) from the Eocene Kishenehn Formation, Montana, USA
Palaeontologia Electronica palaeo-electronica.org Latiblattella avita sp. nov. (Blattaria: Ectobiidae) from the Eocene Kishenehn Formation, Montana, USA Dale E. Greenwalt and Ľubomír Vidlička ABSTRACT Latiblattella avita Greenwalt and Vidlička, 2015, sp. nov., and the first fossil of the genus, is described. The discovery of a fossil representative of this genus suggests that Latiblattella was more widely distributed in the Eocene. The Eocene American cockroach fauna is mostly comprised of what are today, cosmopolitan genera while the extant genus Latiblattella Hebard, 1917 is restricted in its geographical distribution to Central America, Mexico, Florida and Arizona. The discovery of Latiblattella avita, in combination with the recent description of Cariblattoides labandeirai Vršansky et al., 2012, also documents the presence of rather derived representatives of the family Ectobiidae as early as the Middle Eocene. Dale E. Greenwalt. Department of Paleobiology, NMNH, Smithsonian Institution, Washington, District of Columbia, U.S.A. 20013-7012, [email protected]. Ľubomír Vidlička. Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 06 Bratislava, Slovakia, [email protected] and Department of Zoology, Faculty of Natural Sciences, Comenius University, Mlynská dolina, Bratislava, 811 04, Slovakia Keywords: Fossil insect; Cenozoic cockroaches; Pseudophyllodromiinae; new species INTRODUCTION species (Vishniakova, 1973; Zompro and Fritzsche, 1999; Bohn et al., 2010; Vršanský, 2007; Cockroaches form one of the taxonomically 2010; Vršanský and Chorvat, 2013 – but see smaller insect orders with only about 5,000 living Greven and Zwanzig, 2013). Extinct species num- species, the majority of which are found in tropical ber over 1,000 but nearly 80% of these are Paleo- forests (Vidlička, 2001; Vršanský et al., 2002; Roth, zoic “roachoids” (Mitchell, 2013).