Suborder Oribatida Van Der Hammen, 1968. In: Zhang, Z.-Q
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Comparative Functional Morphology of Attachment Devices in Arachnida
Comparative functional morphology of attachment devices in Arachnida Vergleichende Funktionsmorphologie der Haftstrukturen bei Spinnentieren (Arthropoda: Arachnida) DISSERTATION zur Erlangung des akademischen Grades doctor rerum naturalium (Dr. rer. nat.) an der Mathematisch-Naturwissenschaftlichen Fakultät der Christian-Albrechts-Universität zu Kiel vorgelegt von Jonas Otto Wolff geboren am 20. September 1986 in Bergen auf Rügen Kiel, den 2. Juni 2015 Erster Gutachter: Prof. Stanislav N. Gorb _ Zweiter Gutachter: Dr. Dirk Brandis _ Tag der mündlichen Prüfung: 17. Juli 2015 _ Zum Druck genehmigt: 17. Juli 2015 _ gez. Prof. Dr. Wolfgang J. Duschl, Dekan Acknowledgements I owe Prof. Stanislav Gorb a great debt of gratitude. He taught me all skills to get a researcher and gave me all freedom to follow my ideas. I am very thankful for the opportunity to work in an active, fruitful and friendly research environment, with an interdisciplinary team and excellent laboratory equipment. I like to express my gratitude to Esther Appel, Joachim Oesert and Dr. Jan Michels for their kind and enthusiastic support on microscopy techniques. I thank Dr. Thomas Kleinteich and Dr. Jana Willkommen for their guidance on the µCt. For the fruitful discussions and numerous information on physical questions I like to thank Dr. Lars Heepe. I thank Dr. Clemens Schaber for his collaboration and great ideas on how to measure the adhesive forces of the tiny glue droplets of harvestmen. I thank Angela Veenendaal and Bettina Sattler for their kind help on administration issues. Especially I thank my students Ingo Grawe, Fabienne Frost, Marina Wirth and André Karstedt for their commitment and input of ideas. -
Coleoptera: Staphylinidae: Scydmaeninae) on Oribatid and Uropodine Mites: Prey Preferences and Hunting Behaviour
Eur. J. Entomol. 112(1): 151–164, 2015 doi: 10.14411/eje.2015.023 ISSN 12105759 (print), 18028829 (online) Feeding of Scydmaenus rufus (Coleoptera: Staphylinidae: Scydmaeninae) on oribatid and uropodine mites: Prey preferences and hunting behaviour Paweł JAŁOSZYŃSKI 1 and ZIEMOWIT OLSZANOWSKI 2 1 Museum of Natural History, University of Wrocław, Sienkiewicza 21, 50-335 Wrocław, Poland; e-mail: [email protected] 2 Department of Animal Taxonomy and Ecology, A. Mickiewicz University, Umultowska 89, 61-614 Poznań, Poland; e-mail: [email protected] Key words. Coleoptera, Staphylinidae, Scydmaeninae, Scydmaenini, Scydmaenus, Palaearctic, prey preferences, feeding behaviour, Oribatida, Uropodina Abstract. Prey preferences and feeding-related behaviour of a Central European species of Scydmaeninae, Scydmaenus rufus, were studied under laboratory conditions. Results of prey choice experiments involving 22 identified species of mites belonging to 13 families of Oribatida and two families of Mesostigmata (Uropodina) demonstrated that this beetle feeds mostly on oribatid Schelorib atidae (60.38% of prey) and Oppiidae (29.75%) and only occasionally on uropodine Urodinychidae (4.42%) and oribatid Mycobatidae (3.39%); species belonging to Trematuridae (Uropodina), Ceratozetidae and Tectocepheidae (Oribatida) were consumed occasionally. The number of mites consumed per beetle per day was 1.42, and when Oppia nitens was the prey, the entire feeding process took 2.93–5.58 h. Observations revealed that mechanisms for overcoming the prey’s defences depended on the body form of the mite. When attacking oribatids, with long and spiny legs, the beetles cut off one or two legs before killing the mite by inserting one mandible into its gnathosomal opening. -
Risk of Exposure of a Selected Rural Population in South Poland to Allergenic Mites
Experimental and Applied Acarology https://doi.org/10.1007/s10493-019-00355-7 Risk of exposure of a selected rural population in South Poland to allergenic mites. Part II: acarofauna of farm buildings Krzysztof Solarz1 · Celina Pająk2 Received: 5 September 2018 / Accepted: 27 February 2019 © The Author(s) 2019 Abstract Exposure to mite allergens, especially from storage and dust mites, has been recognized as a risk factor for sensitization and allergy symptoms that could develop into asthma. The aim of this study was to investigate the occurrence of mites in debris and litter from selected farm buildings of the Małopolskie province, South Poland, with particular refer- ence to allergenic and/or parasitic species as a potential risk factor of diseases among farm- ers. Sixty samples of various materials (organic dust, litter, debris and residues) from farm buildings (cowsheds, barns, chaff-cutter buildings, pigsties and poultry houses) were sub- jected to acarological examination. The samples were collected in Lachowice and Kurów (Suski district, Małopolskie). A total of 16,719 mites were isolated including specimens from the cohort Astigmatina (27 species) which comprised species considered as allergenic (e.g., Acarus siro complex, Tyrophagus putrescentiae, Lepidoglyphus destructor, Glycy- phagus domesticus, Chortoglyphus arcuatus and Gymnoglyphus longior). Species of the families Acaridae (A. siro, A. farris and A. immobilis), Glycyphagidae (G. domesticus, L. destructor and L. michaeli) and Chortoglyphidae (C. arcuatus) have been found as numeri- cally dominant among astigmatid mites. The majority of mites were found in cowsheds (approx. 32%) and in pigsties (25.9%). The remaining mites were found in barns (19.6%), chaff-cutter buildings (13.9%) and poultry houses (8.8%). -
Tyrophagus (Acari: Astigmata: Acaridae). Fauna of New Zealand 56, 291 Pp
Fan, Q.-H.; Zhang, Z.-Q. 2007: Tyrophagus (Acari: Astigmata: Acaridae). Fauna of New Zealand 56, 291 pp. INVERTEBRATE SYSTEMATICS ADVISORY GROUP REPRESENTATIVES OF L ANDCARE R ESEARCH Dr D. Choquenot Private Bag 92170, Auckland, New Zealand Dr T.K. Crosby and Dr R. J. B. Hoare Private Bag 92170, Auckland, New Zealand REPRESENTATIVE OF U NIVERSITIES Dr R.M. Emberson Ecology and Entomology Group Soil, Plant, and Ecological Sciences Division P.O. Box 84, Lincoln University, New Zealand REPRESENTATIVE OF M USEUMS Mr R.L. Palma Natural Environment Department Museum of New Zealand Te Papa Tongarewa P.O. Box 467, Wellington, New Zealand REPRESENTATIVE OF O VERSEAS I NSTITUTIONS Dr M. J. Fletcher Director of the Collections NSW Agricultural Scientific Collections Unit Forest Road, Orange NSW 2800, Australia * * * SERIES EDITOR Dr T. K. Crosby Private Bag 92170, Auckland, New Zealand Fauna of New Zealand Ko te Aitanga Pepeke o Aotearoa Number / Nama 56 Tyrophagus (Acari: Astigmata: Acaridae) Qing-Hai Fan Institute of Natural Resources, Massey University, Palmerston North, New Zealand, and College of Plant Protection, Fujian Agricultural and Forestry University, Fuzhou 350002, China [email protected] and Zhi-Qiang Zhang Landcare Research, P rivate Bag 92170, Auckland, New Zealand [email protected] Manaak i W h e n u a P R E S S Lincoln, Canterbury, New Zealand 2007 Copyright © Landcare Research New Zealand Ltd 2007 No part of this work covered by copyright may be reproduced or copied in any form or by any means (graphic, electronic, or mechanical, including photocopying, recording, taping information retrieval systems, or otherwise) without the written permission of the publisher. -
Coleoptera: Staphylinidae: Scydmaeninae) on Oribatid Mites: Prey Preferences and Hunting Behaviour
Eur. J. Entomol. 110(2): 339–353, 2013 http://www.eje.cz/pdfs/110/2/339 ISSN 1210-5759 (print), 1802-8829 (online) Specialized feeding of Euconnus pubicollis (Coleoptera: Staphylinidae: Scydmaeninae) on oribatid mites: Prey preferences and hunting behaviour 1 2 PAWEŁ JAŁOSZYŃSKI and ZIEMOWIT OLSZANOWSKI 1 Museum of Natural History, Wrocław University, Sienkiewicza 21, 50-335 Wrocław, Poland; e-mail: [email protected] 2 Department of Animal Taxonomy and Ecology, A. Mickiewicz University, Umultowska 89, 61-614 Poznań, Poland; e-mail: [email protected] Key words. Coleoptera, Staphylinidae, Scydmaeninae, Cyrtoscydmini, Euconnus, Palaearctic, prey preferences, feeding behaviour, Acari, Oribatida Abstract. Prey preferences and feeding-related behaviour of a Central European species of Scydmaeninae, Euconnus pubicollis, were studied under laboratory conditions. Results of prey choice experiments involving 50 species of mites belonging to 24 families of Oribatida and one family of Uropodina demonstrated that beetles feed mostly on ptyctimous Phthiracaridae (over 90% of prey) and only occasionally on Achipteriidae, Chamobatidae, Steganacaridae, Oribatellidae, Ceratozetidae, Euphthiracaridae and Galumni- dae. The average number of mites consumed per beetle per day was 0.27 ± 0.07, and the entire feeding process took 2.15–33.7 h and showed a clear linear relationship with prey body length. Observations revealed a previously unknown mechanism for capturing prey in Scydmaeninae in which a droplet of liquid that exudes from the mouth onto the dorsal surface of the predator’s mouthparts adheres to the mite’s cuticle. Morphological adaptations associated with this strategy include the flattened distal parts of the maxillae, whereas the mandibles play a minor role in capturing prey. -
A New Species of the Feather Mite Genus Analges Nitzsch
Acarina 27 (1): 19–43 © Acarina 2019 A NEW SPECIES OF THE FEATHER MITE GENUS ANALGES NITZSCH, 1818 (ACARIFORMES: ANALGIDAE) FROM THE STREAKED SPIDERHUNTER ARACHNOTHERA MAGNA (PASSERIFORMES: NECTARINIIDAE), WITH A RENEWED DIAGNOSIS AND WORLD CHECKLIST TO THE GENUS Sergey V. Mironov Zoological Institute, Russian Academy of Sciences, Saint Petersburg, Russia; e-mail: [email protected] ABSTRACT: A renewed generic diagnosis of the genus Analges Nitzsch, 1818 (Analgidae: Analginae) is proposed, and several corrections in the species content and taxonomic structure of the genus Analges are made. Designation of Analges passerinus (Linnaeus, 1758) as a type species of the genus Analges by von Heyden (1826) has indisputable priority over A. chelopus (Her- mann, 1804) as designated by Trouessart (1916) and incorrectly used by many subsequent researchers. Therefore, the subgenus Analgopsis Trouessart, 1919, which was established with the same type species, A. passerinus, is here synonymized with the genus Analges. The monotypic genus Plesialges Trouessart 1919, placed by Gaud and Atyeo (1996) into the genus Analges Nitzsch, 1818 and so far treated as a subgenus, is removed from Analges and suggested to be a distinct genus. In the concept proposed herein, the genus Analges is not subdivided into subgenera, but several of its species are arranged into two newly established species groups: chelopus and passerinus. A new feather mite species Analges arachnotherae sp. n. is described from Arachnothera magna (Hodgson) (Nectariniidae) from Vietnam. A world checklist of species of Analges is provided for the first time and includes 64 valid species names. It also includes synonyms and important misidentifications and provides comments to complicate taxonomic cases. -
Kiwi First Aid and Veterinary Care
9. Acknowledgements Special thanks to Dr Brett Gartrell, Massey University, and Richard Jakob-Hoff, Auckland Zoo, for peer reviewing this document. Thanks also to Dr Maurice Alley, Massey University, and Kate McInnes, Department of Conservation, for their contributions. Jenny Youl and Vanessa Gray (Massey University), Trevor Kelly (The Vet Centre, Rotorua) and Claire Travers (Kiwi Encounter, Rainbow Springs, Rotorua) are acknowledged for the use of their photos. Dallas Bishop (Agresearch) and Ricardo Palma (Te Papa Tongarewa, Museum of New Zealand) confirmed the accuracy of the ectoparasites recorded from kiwi listed in Table 3. 10. References Abou-Madi, N.; Kollias, G.V. (Eds) 1992: Avian fluid therapy. Current veterinary therapy XI. W.B. Co, Philadelphia. Aguilar, R.F. 2004: The use of occlusive hydrocolloidal bandages in raptor wound management. Pp. 135–137 in: Proceedings of the Australian Committee of the Association of Avian Veterinarians, Kakadu. Andrews, J.R.H. 1977: A new species of Lyperosomum (Digenea: Dicrocoeliidae) from the North Island brown kiwi. New Zealand Journal of Zoology 4: 99–100. Bauck, L. 1994: Mycoses. Pp. 997–1006 in Ritchie, B.W.; Harrison, G.J.; Harrison, L.R. (Eds): Avian medicine: principles and application. Wingers Publishing Inc., Lake Worth, Florida. Bauck, L.; Kupersmith, D. 1991: Intraosseous fluids. Journal of the Association of Avian Veterinarians 5: 74–100. Benham, W.B. 1990: The structure of the rostellum in two new species of tapeworm, from Apteryx. Quarterly Journal of Microscopical Science 43: 83–96. Bennett, R.A. 1994: Neurology. Pp. 723–747 in Ritchie, B.W.; Harrison, G.J.; Harrison, L.R. (Eds): Avian medicine: principles and application. -
Assessing Symbiont Extinction Risk Using Cophylogenetic Data 2 3 Jorge Doña1 and Kevin P
1 Assessing symbiont extinction risk using cophylogenetic data 2 3 Jorge Doña1 and Kevin P. Johnson1 4 5 1. Illinois Natural History Survey, Prairie Research Institute, University of Illinois at Urbana-Champaign, 6 1816 S. Oak St., Champaign, IL 61820, USA 7 8 *Corresponding authors: Jorge Doña & Kevin Johnson; e-mail: [email protected] & [email protected] 9 10 Abstract: Symbionts have a unique mode of life that has attracted the attention of ecologists and 11 evolutionary biologists for centuries. As a result of this attention, these disciplines have produced 12 a mature body of literature on host-symbiont interactions. In contrast, the discipline of symbiont 13 conservation is still in a foundational stage. Here, we aim to integrate methodologies on symbiont 14 coevolutionary biology with the perspective of conservation. We focus on host-symbiont 15 cophylogenies, because they have been widely used to study symbiont diversification history and 16 contain information on symbiont extinction. However, cophylogenetic information has never been 17 used nor adapted to the perspective of conservation. Here, we propose a new statistic, 18 “cophylogenetic extinction rate” (Ec), based on coevolutionary knowledge, that uses data from 19 event-based cophylogenetic analyses, and which could be informative to assess relative symbiont 20 extinction risks. Finally, we propose potential future research to further develop estimation of 21 symbiont extinction risk from cophylogenetic analyses and continue the integration of this existing 22 knowledge of coevolutionary biology and cophylogenetics into future symbiont conservation 23 studies and practices. 24 25 Keywords: coevolution, coextinction risk, conservation biology, cophylogenies, host-symbiont 26 interactions, parasites. -
IV. the Oribatid Mites (Acari: Cryptostigmata)
This file was created by scanning the printed publication. Text errors identified by the software have been corrected; however, some errors may remain. United States Department of Invertebrates of the H.J. Agriculture Andrews Experimental Forest Service Pacific Northwest Forest, Western Cascade Research Station General Technical Report Mountains, Oregon: IV. PNW-217 August 1988 The Oribatid Mites (Acari: Cryptostigmata) Andrew R. Moldenke and Becky L. Fichter I ANDREW MOLDENKE and BECKY FICHTER are Research Associates, Department of Entomology, Oregon State University, Corvallis, Oregon 97331. TAXONOMIC LISTING OF PACIFIC NORTHWEST GENERA * - indicates definite records from the Pacific Northwest *Maerkelotritia 39-40, figs. 83-84 PALAEOSOMATA (=BIFEMORATINA) (=Oribotritia sensu Walker) Archeonothroidea *Mesotritia 40 *Acaronychus 32, fig. 64 *Microtritia 40-41, fig. 85 *Zachvatkinella 32, fig. 63 *Oribotritia 39, figs. 81-82 Palaeacaroidea Palaeacarus 32, fig. 61 (=Plesiotritia) *Rhysotritia 40 Ctenacaroidea *Aphelacarus 32, fig. 59 *Synichotritia 41 Beklemishevia 32, fig. 62 Perlohmannioidea *Perlohmannia 65, figs. 164-166, 188 *Ctenacarus 32, fig. 60 ENARTHRONOTA (=ARTHRONOTINA) Epilohmannioidea *Epilohmannia 65-66, figs. 167-169, Brachychthonioidea 187 *Brachychthonius 29-30, fig. 53 Eulohmannioidea *Eobrachychthonius 29 *Eulohmannia 35, figs. 67-68 *Liochthonius 29, figs. 54,55,306 DESMONOMATA Mixochthonius 29 Crotonioidea (=Nothroidea) Neobrachychthonius 29 *Camisia 36, 68. figs. 70-71, Neoliochthonius 29 73, 177-178, 308 (=Paraliochthonius) Heminothrus 71 Poecilochthonius 29 *Malaconothrus 36, fig. 74 *Sellnickochthonius 29, figs. 56-57 Mucronothrus 36 (=Brachychochthonius) Neonothrus 71 *Synchthonius 29 *Nothrus 69, fig. 179-182, Verachthonius 29 186, 310 Hypochthonioidea *Platynothrus 71, figs. 183-185 *Eniochthonius 28, figs. 51-52 309 (=Hypochthoniella) *Trhypochthonius 35, fig. 69 *Eohypochthonius 27-28, figs. 44-45 *Hypochthonius 28, figs. -
Oribatida No
13 (2) · 2013 Franke, K. Oribatida No. 44 ...................................................................................................................................................................................... 1 – 24 Acarological literature .................................................................................................................................................................... 1 Publications 2013 ........................................................................................................................................................................................... 1 Publications 2012 ........................................................................................................................................................................................... 5 Publications, additions 2011 ........................................................................................................................................................................ 10 Publications, additions 2010 ....................................................................................................................................................................... 10 Publications, additions 2009 ....................................................................................................................................................................... 10 Publications, additions 2008 ...................................................................................................................................................................... -
Three Feather Mites(Acari: Sarcoptiformes: Astigmata)
Journal of Species Research 8(2):215-224, 2019 Three feather mites (Acari: Sarcoptiformes: Astigmata) isolated from Tringa glareola in South Korea Yeong-Deok Han and Gi-Sik Min* Department of Biological Sciences, Inha University, Incheon 22212, Republic of Korea *Correspondent: [email protected] We describe three feather mites recovered from a wood sandpiper Tringa glareola that was stored in a -20°C freezer at the Chungnam Wild Animal Rescue Center. These feather mites are reported for the first time in South Korea: Avenzoaria totani (Canestrini, 1978), Ingrassia veligera Oudemans, 1904 and Mon tchadskiana glareolae Dabert and Ehrnsberger, 1999. In this study, we provide morphological diagnoses and illustrations. Additionally, we provide partial sequences of the mitochondrial cytochrome c oxidase subunit I (COI) gene as molecular characteristics of three species. Keywords: Avenzoaria totani, COI, feather mite, Ingrassia veligera, Montchadskiana glareolae, wood sandpiper, South Korea Ⓒ 2019 National Institute of Biological Resources DOI:10.12651/JSR.2019.8.2.215 INTRODUCTION is absent in males (Vasjukova and Mironov, 1991). The genus Montchadskiana is one of five genera that The wood sandpiper Tringa glareola (Linnaeus, 1758) belong to the subfamily Magimeliinae Gaud, 1972 and inhabits swamp and marshes (wet heathland, spruce or contains 17 species (Gaud and Atyeo, 1996; Dabert and birch forest) in the northern Eurasian continent (Pulliain- Ehrnsberger, 1999). This genus was found on flight feath- en and Saari, 1991; del Hoyo et al., -
Terrestrial Arthropods)
Fall 2004 Vol. 23, No. 2 NEWSLETTER OF THE BIOLOGICAL SURVEY OF CANADA (TERRESTRIAL ARTHROPODS) Table of Contents General Information and Editorial Notes..................................... (inside front cover) News and Notes Forest arthropods project news .............................................................................51 Black flies of North America published...................................................................51 Agriculture and Agri-Food Canada entomology web products...............................51 Arctic symposium at ESC meeting.........................................................................51 Summary of the meeting of the Scientific Committee, April 2004 ..........................52 New postgraduate scholarship...............................................................................59 Key to parasitoids and predators of Pissodes........................................................59 Members of the Scientific Committee 2004 ...........................................................59 Project Update: Other Scientific Priorities...............................................................60 Opinion Page ..............................................................................................................61 The Quiz Page.............................................................................................................62 Bird-Associated Mites in Canada: How Many Are There?......................................63 Web Site Notes ...........................................................................................................71