(Soft) Ticks (Acari: Parasitiformes: Argasidae) in Relation to Transmission of Human Pathogens
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The Predatory Mite (Acari, Parasitiformes: Mesostigmata (Gamasina); Acariformes: Prostigmata) Community in Strawberry Agrocenosis
Acta Universitatis Latviensis, Biology, 2004, Vol. 676, pp. 87–95 The predatory mite (Acari, Parasitiformes: Mesostigmata (Gamasina); Acariformes: Prostigmata) community in strawberry agrocenosis Valentîna Petrova*, Ineta Salmane, Zigrîda Çudare Institute of Biology, University of Latvia, Miera 3, Salaspils LV-2169, Latvia *Corresponding author, E-mail: [email protected]. Abstract Altogether 37 predatory mite species from 14 families (Parasitiformes and Acariformes) were collected using leaf sampling and pit-fall trapping in strawberry fi elds (1997 - 2001). Thirty- six were recorded on strawberries for the fi rst time in Latvia. Two species, Paragarmania mali (Oud.) (Aceosejidae) and Eugamasus crassitarsis (Hal.) (Parasitidae) were new for the fauna of Latvia. The most abundant predatory mite families (species) collected from strawberry leaves were Phytoseiidae (Amblyseius cucumeris Oud., A. aurescens A.-H., A. bicaudus Wainst., A. herbarius Wainst.) and Anystidae (Anystis baccarum L.); from pit-fall traps – Parasitidae (Poecilochirus necrophori Vitz. and Parasitus lunaris Berl.), Aceosejidae (Leioseius semiscissus Berl.) and Macrochelidae (Macrocheles glaber Müll). Key words: agrocenosis, diversity, predatory mites, strawberry. Introduction Predatory mites play an important ecological role in terrestrial ecosystems and they are increasingly being used in management for biocontrol of pest mites, thrips and nematodes (Easterbrook 1992; Wright, Chambers 1994; Croft et al. 1998; Cuthbertson et al. 2003). Many of these mites have a major infl uence on nutrient cycling, as they are predators on other arthropods (Santos 1985; Karg 1993; Koehler 1999). In total, investigations of mite fauna in Latvia were made by Grube (1859), who found 28 species, Eglītis (1954) – 50 species, Kuznetsov and Petrov (1984) – 85 species, Lapiņa (1988) – 207 species, and Salmane (2001) – 247 species. -
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. -
Ticks (Parasitiformes: Ixodida) on New World Wild Primates in Brazil
International Journal of Acarology ISSN: (Print) (Online) Journal homepage: https://www.tandfonline.com/loi/taca20 Ticks (Parasitiformes: Ixodida) on new world wild primates in Brazil Thiago F. Martins, Rodrigo H. F. Teixeira, Julio C. Souza Jr, Hermes R. Luz, Mônica M. Montenegro, Leandro Jerusalinsky, Marina G. Bueno, Valeria C. Onofrio, Marinete Amorim, Gilberto S. Gazêta, Paula De J. Da Silva, Karla Bitencourth, Ana B. P. Borsoi, Sandro Marques, Marco O. Mattos Jr, Leandra S. I. Hernandes, Alessandra Scofild, Rafael F. C. Vieira, Richard C. Pacheco, Maurício C. Horta, Valéria P. da Silva, Patrícia W. Silva, Claudia A. Igayara, Thais C. Sanches, Marcello S. Nardi, Camile Lugarini, Natasha L. Maia, Cláudio L. M. de Siqueira, Juliana M. Ferreira, João F. Soares & Marcelo B. Labruna To cite this article: Thiago F. Martins, Rodrigo H. F. Teixeira, Julio C. Souza Jr, Hermes R. Luz, Mônica M. Montenegro, Leandro Jerusalinsky, Marina G. Bueno, Valeria C. Onofrio, Marinete Amorim, Gilberto S. Gazêta, Paula De J. Da Silva, Karla Bitencourth, Ana B. P. Borsoi, Sandro Marques, Marco O. Mattos Jr, Leandra S. I. Hernandes, Alessandra Scofild, Rafael F. C. Vieira, Richard C. Pacheco, Maurício C. Horta, Valéria P. da Silva, Patrícia W. Silva, Claudia A. Igayara, Thais C. Sanches, Marcello S. Nardi, Camile Lugarini, Natasha L. Maia, Cláudio L. M. de Siqueira, Juliana M. Ferreira, João F. Soares & Marcelo B. Labruna (2021): Ticks (Parasitiformes: Ixodida) on new world wild primates in Brazil, International Journal of Acarology, DOI: 10.1080/01647954.2020.1870554 To link to this article: https://doi.org/10.1080/01647954.2020.1870554 Published online: 03 Mar 2021. -
Gamasid Mites
NATIONAL RESEARCH TOMSK STATE UNIVERSITY BIOLOGICAL INSTITUTE RUSSIAN ACADEMY OF SCIENCE ZOOLOGICAL INSTITUTE M.V. Orlova, M.K. Stanyukovich, O.L. Orlov GAMASID MITES (MESOSTIGMATA: GAMASINA) PARASITIZING BATS (CHIROPTERA: RHINOLOPHIDAE, VESPERTILIONIDAE, MOLOSSIDAE) OF PALAEARCTIC BOREAL ZONE (RUSSIA AND ADJACENT COUNTRIES) Scientific editor Andrey S. Babenko, Doctor of Science, professor, National Research Tomsk State University Tomsk Publishing House of Tomsk State University 2015 UDK 576.89:599.4 BBK E693.36+E083 Orlova M.V., Stanyukovich M.K., Orlov O.L. Gamasid mites (Mesostigmata: Gamasina) associated with bats (Chiroptera: Vespertilionidae, Rhinolophidae, Molossidae) of boreal Palaearctic zone (Russia and adjacent countries) / Scientific editor A.S. Babenko. – Tomsk : Publishing House of Tomsk State University, 2015. – 150 р. ISBN 978-5-94621-523-7 Bat gamasid mites is a highly specialized ectoparasite group which is of great interest due to strong isolation and other unique features of their hosts (the ability to fly, long distance migration, long-term hibernation). The book summarizes the results of almost 60 years of research and is the most complete summary of data on bat gamasid mites taxonomy, biology, ecol- ogy. It contains the first detailed description of bat wintering experience in sev- eral regions of the boreal Palaearctic. The book is addressed to zoologists, ecologists, experts in environmental protection and biodiversity conservation, students and teachers of biology, vet- erinary science and medicine. UDK 576.89:599.4 -
Tick Saliva and Its Role in Pathogen Transmission
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by NERC Open Research Archive lyme borreliosis Wien Klin Wochenschr https://doi.org/10.1007/s00508-019-1500-y Tick saliva and its role in pathogen transmission Patricia A. Nuttall Received: 22 February 2019 / Accepted: 9 April 2019 © The Author(s) 2019 Summary Tick saliva is a complex mixture of peptidic cle of egg, larva, nymph, and adult (female or male). and non-peptidic molecules that aid engorgement. Each postembryonic stage generally requires a blood The composition of tick saliva changes as feeding meal before moulting to the next stage [2]. During progresses and the tick counters the dynamic host blood-feeding, ticks acquire infections they may sub- response. Ixodid ticks such as Ixodes ricinus,the sequently transmit when feeding again. When this most important tick species in Europe, transmit nu- occurs, ticks act as vectors of potential pathogens of merous pathogens that cause debilitating diseases, humans and other animals [3]. In fact, ticks are be- e.g. Lyme borreliosis and tick-borne encephalitis. lieved to transmit the greatest variety of infectious Tick-borne pathogens are transmitted in tick saliva agents of any blood-feeding vector. Notable diseases during blood feeding; however, saliva is not simply of humans caused by tick-borne pathogens include a medium enabling pathogen transfer. Instead, tick- Lyme borreliosis, tick-borne encephalitis (TBE), tu- borne pathogens exploit saliva-induced modulation laremia, babesiosis, rickettsiosis, and human granu- of host responses to promote their transmission and locytic anaplasmosis; however, tick-borne infectious infection, so-called saliva-assisted transmission (SAT). -
Community Structure of Mites (Acari: Acariformes and Parasitiformes) in Nests of the Semi-Collared Flycatcher (Ficedula Semitorquata) R
International Research Journal of Natural Sciences Vol.3, No.3, pp.48-53, December 2015 ___Published by European Centre for Research Training and Development UK (www.eajournals.org) COMMUNITY STRUCTURE OF MITES (ACARI: ACARIFORMES AND PARASITIFORMES) IN NESTS OF THE SEMI-COLLARED FLYCATCHER (FICEDULA SEMITORQUATA) R. Davidova, V. Vasilev, N. Ali, J. Bakalova Konstantin Preslavsky University of Shumen, 115, Universitetska Str., Shumen, 9700, Bulgaria. ABSTRACT: The aims of the present paper are to establish the specific structure of communities of prostigmatic and mesostigmatic mites in nests of the semi-collared flycatcher (Ficedula semitorquata) and to compare the fauna with the mites in nests of two other European flycatchers. For analysis of community structure of mites were used the indices: prevalence, relative density, mean intensity and dominance. Mite communities are strongly dominated by the species Dermanyssus gallinae and Ornithonyssus sylviarum, which were found with the highest frequency and dominance. The mite communities are characterized by a large number of subrecedent species. KEYWORDS: Acariformes, Parasitiformes, Nest of Bird, Community Structure INTRODUCTION The nests of different species of birds are an example of a fairly unstable and isolated habitat, with its own dependent on it specific fauna which involves different groups of invertebrate animals. One of the components of this fauna which demonstrates particular abundance is the arthropods, and more specifically, the mites. The studies of Parasitiformes show that mesostigmatic mites living in birds' nests vary both in terms of their species affiliation and the structure of their communities [4, 8]. Highly important with respect to veterinary science and medicine are a number of species, such as Ornithonyssus bursa, Ornithonyssus sylviarum, Dermanyssus gallinae harboured by birds, Ornithonyssus bacoti, harboured by rodents, etc. -
Introduction to Arthropod Groups What Is Entomology?
Entomology 340 Introduction to Arthropod Groups What is Entomology? The study of insects (and their near relatives). Species Diversity PLANTS INSECTS OTHER ANIMALS OTHER ARTHROPODS How many kinds of insects are there in the world? • 1,000,0001,000,000 speciesspecies knownknown Possibly 3,000,000 unidentified species Insects & Relatives 100,000 species in N America 1,000 in a typical backyard Mostly beneficial or harmless Pollination Food for birds and fish Produce honey, wax, shellac, silk Less than 3% are pests Destroy food crops, ornamentals Attack humans and pets Transmit disease Classification of Japanese Beetle Kingdom Animalia Phylum Arthropoda Class Insecta Order Coleoptera Family Scarabaeidae Genus Popillia Species japonica Arthropoda (jointed foot) Arachnida -Spiders, Ticks, Mites, Scorpions Xiphosura -Horseshoe crabs Crustacea -Sowbugs, Pillbugs, Crabs, Shrimp Diplopoda - Millipedes Chilopoda - Centipedes Symphyla - Symphylans Insecta - Insects Shared Characteristics of Phylum Arthropoda - Segmented bodies are arranged into regions, called tagmata (in insects = head, thorax, abdomen). - Paired appendages (e.g., legs, antennae) are jointed. - Posess chitinous exoskeletion that must be shed during growth. - Have bilateral symmetry. - Nervous system is ventral (belly) and the circulatory system is open and dorsal (back). Arthropod Groups Mouthpart characteristics are divided arthropods into two large groups •Chelicerates (Scissors-like) •Mandibulates (Pliers-like) Arthropod Groups Chelicerate Arachnida -Spiders, -
Ixodida: Argasidae) En México
Universidad Nacional Autónoma de México Facultad de Estudios Superiores – Zaragoza Diferenciación morfológica y molecular de garrapatas del género Antricola (Ixodida: Argasidae) en México. TESIS Que para obtener el título de: BIÓLOGO Presenta: Jesús Alberto Lugo Aldana Directora de tesis: Dra. María del Carmen Guzmán Cornejo Asesor interno: Dr. David Nahum Espinosa Organista México, D. F. Abril 2013 Facultad de Estudios Superiores Zaragoza, UNAM. *** Laboratorio de Acarología “Anita Hoffman” Facultad de Ciencias, UNAM. Dedicatoria A mi esposa Diana Sánchez y mi pequeña princesa Quetzalli por ser el motivo, para ser mejor día con día. A mi mamá Sara H. Aldana G. y mi papá Jesús G. Lugo C. por enseñarme los valores que hoy me hacen ser una gran persona, además de ser el ejemplo para superarme todos los días. A mi hermana Mitzi Saraí y hermano José Luis por su apoyo incondicional, que además de ser inspiración, lograron alentarme en todo momento para concluir este gran proyecto. A la familia Aldana Sánchez, Aldana Godínez, Del Moral Aldana, Lugo Cid, Lugo Romero, Lugo Maldonado y a la Sra. Irene Cabrera R., por todos sus consejos y apoyo incondicional a lo largo de toda mi carrera. Mil gracias… Agradecimientos o A mi alma mater U.N.A.M., por darme la oportunidad de ser parte de ésta gran institución. o A la Facultad de Estudios Superiores Zaragoza, por brindarme los conocimientos esenciales en toda mi formación como biólogo. o A la Dra. Ma. Del Carmen Guzmán Cornejo, “Meli”, por todo su apoyo incondicional durante la realización de éste trabajo, ya que sin sus consejos, orientación, confianza y amistad no se hubieran alcanzado tantas satisfacciones. -
Crimean-Congo Hemorrhagic Fever
Crimean-Congo Importance Crimean-Congo hemorrhagic fever (CCHF) is caused by a zoonotic virus that Hemorrhagic seems to be carried asymptomatically in animals but can be a serious threat to humans. This disease typically begins as a nonspecific flu-like illness, but some cases Fever progress to a severe, life-threatening hemorrhagic syndrome. Intensive supportive care is required in serious cases, and the value of antiviral agents such as ribavirin is Congo Fever, still unclear. Crimean-Congo hemorrhagic fever virus (CCHFV) is widely distributed Central Asian Hemorrhagic Fever, in the Eastern Hemisphere. However, it can circulate for years without being Uzbekistan hemorrhagic fever recognized, as subclinical infections and mild cases seem to be relatively common, and sporadic severe cases can be misdiagnosed as hemorrhagic illnesses caused by Hungribta (blood taking), other organisms. In recent years, the presence of CCHFV has been recognized in a Khunymuny (nose bleeding), number of countries for the first time. Karakhalak (black death) Etiology Crimean-Congo hemorrhagic fever is caused by Crimean-Congo hemorrhagic Last Updated: March 2019 fever virus (CCHFV), a member of the genus Orthonairovirus in the family Nairoviridae and order Bunyavirales. CCHFV belongs to the CCHF serogroup, which also includes viruses such as Tofla virus and Hazara virus. Six or seven major genetic clades of CCHFV have been recognized. Some strains, such as the AP92 strain in Greece and related viruses in Turkey, might be less virulent than others. Species Affected CCHFV has been isolated from domesticated and wild mammals including cattle, sheep, goats, water buffalo, hares (e.g., the European hare, Lepus europaeus), African hedgehogs (Erinaceus albiventris) and multimammate mice (Mastomys spp.). -
Tick ID Card
tick removal Remove ticks immediately. They usually need to attach for 24 hours to transmit Lyme disease. tickknow them. prevent ID them. Consult a physician if you remove an engorged deer tick. Using a tick spoon: Deer Tick (Black-Legged Tick) • Place the wide part of the notch on the skin near the tick (hold skin taut if necessary) • Applying slight pressure downward on the nymph adult male adult female skin, slide the remover forward so the small part of the notch is framing the tick • Continuous sliding motion of the remover (actual size) detaches the tick nymph adult engorged adult Using tweezers: (1/32"–1/16") (1/8") (up to 1/2") • Grasp the tick close to the skin with tweezers • Pull gently until the tick lets go Dog Tick 1-800-821-5821 www.mainepublichealth.gov adult male adult female (examples are not actual size, dog tick nymphs are rarely found on humans or their pets) 0" 2" just the facts lyme disease Deer Ticks Ticks usually need to attach for 24 hours • Deer ticks may transmit the agents that to transmit Lyme disease. cause Lyme disease, anaplasmosis, and Often, people see an expanding red babesiosis rash (or bull’s-eye rash) more than • What bites: nymphs and adult females 2 inches across at the site of the • When: anytime temperatures are above tick bite, which may occur within a freezing, greatest risk is spring through fall few days or a few weeks. Dog Ticks Other symptoms include: • • Dog ticks do not transmit the agent that fatigue causes Lyme disease • muscle and joint pain • What bites: adult females • headache • When: April–August • fever and chills • facial paralysis Deer ticks may also transmit the agents prevent the bite that cause other diseases such as babesia • Wear light-colored protective clothing and anaplasmosis. -
The External Parasites of Birds: a Review
THE EXTERNAL PARASITES OF BIRDS: A REVIEW BY ELIZABETH M. BOYD Birds may harbor a great variety and numher of ectoparasites. Among the insects are biting lice (Mallophaga), fleas (Siphonaptera), and such Diptera as hippohoscid flies (Hippohoscidae) and the very transitory mosquitoes (Culicidae) and black flies (Simuliidae), which are rarely if every caught on animals since they fly off as soon as they have completed their blood-meal. One may also find, in birds ’ nests, bugs of the hemipterous family Cimicidae, and parasitic dipterous larvae that attack nestlings. Arachnida infesting birds comprise the hard ticks (Ixodidae), soft ticks (Argasidae), and certain mites. Most ectoparasites are blood-suckers; only the Ischnocera lice and some species of mites subsist on skin components. The distribution of ectoparasites on the host varies with the parasite concerned. Some show no habitat preference while others tend to confine themselves to, or even are restricted to, definite areas on the body. A list of 198 external parasites for 2.55 species and/or subspecies of birds east of the Mississippi has been compiled by Peters (1936) from files of the Bureau of Entomology and Plant Quarantine between 1928 and 1935. Fleas and dipterous larvae were omitted from this list. According to Peters, it is possible to collect three species of lice, one or two hippoboscids, and several types of mites on a single bird. He records as many as 15 species of ectoparasites each from the Bob-white (Co&us uirginianus), Song Sparrow (Melospiza melodia), and Robin (Turdus migratorius). The lice and plumicolous mites, however, are typically the most abundant forms present on avian hosts. -
Germany) 185- 190 ©Zoologische Staatssammlung München;Download
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Spixiana, Zeitschrift für Zoologie Jahr/Year: 2004 Band/Volume: 027 Autor(en)/Author(s): Rupp Doris, Zahn Andreas, Ludwig Peter Artikel/Article: Actual records of bat ectoparasites in Bavaria (Germany) 185- 190 ©Zoologische Staatssammlung München;download: http://www.biodiversitylibrary.org/; www.biologiezentrum.at SPIXIANA 27 2 185-190 München, Ol. Juli 2004 ISSN 0341-8391 Actual records of bat ectoparasites in Bavaria (Germany) Doris Rupp, Andreas Zahn & Peter Ludwig ) Rupp, D. & A. Zahn & P. Ludwig (2004): Actual records of bat ectoparasites in Bavaria (Germany). - Spixiana 27/2: 185-190 Records of ectoparasites of 19 bat species coilected in Bavaria are presented. Altogether 33 species of eight parasitic families of tleas (Ischnopsyllidae), batflies (Nycteribiidae), bugs (Cimicidae), mites (Spinturnicidae, Macronyssidae, Trom- biculidae, Sarcoptidae) and ticks (Argasidae, Ixodidae) were found. Eight species were recorded first time in Bavaria. All coilected parasites are deposited in the collection of the Zoologische Staatsammlung München (ZSM). Doris Rupp, Gailkircher Str. 7, D-81247 München, Germany Andreas Zahn, Zoologisches Institut der LMU, Luisenstr. 14, D-80333 München, Germany Peter Ludwig, Peter Rosegger Str. 2, D-84478 Waldkraiburg, Germany Introduction investigated. The investigated bats belonged to the following species (number of individuals in brack- There are only few reports about bat parasites in ets: Barbastelhis barbastelliis (7) - Eptesicus nilsomi (10) Germany and the Bavarian ectoparasite fauna is - E. serotimis (6) - Myotis bechsteinii (6) - M. brandtii - poorly investigated yet. From 1998 tili 2001 we stud- (20) - M. daubentonii (282) - M. emarginatus (12) ied the parasite load of bats in Bavaria.