(Acari: Heterostigmatina: Scutacaridae) from Soil of Citrus Orchards in Assiut, Egypt Eraky, S.A.; A.S

Total Page:16

File Type:pdf, Size:1020Kb

(Acari: Heterostigmatina: Scutacaridae) from Soil of Citrus Orchards in Assiut, Egypt Eraky, S.A.; A.S Assiut J. Agric. Sci., (50) No. (2) 2019 (200-205) ISSN: 1110-0486 Website: www.aun.edu.eg/faculty_agriculture/journals_issues_form.php E-mail: [email protected] Description of Heterodispus longisetae n. sp. (Acari: Heterostigmatina: Scutacaridae) from Soil of Citrus Orchards in Assiut, Egypt Eraky, S.A.; A.S. Abdelgayed; M.W. Negm; T.Y. Helal1 and S.F.M. Moussa2 1Department of Plant Protection, Faculty of Agriculture, Assiut University, Assiut, Egypt. 2Plant Protection Research Institute, Agricultural Research Center, Dokki, Giza, Egypt. *Corresponding author: [email protected] Received on: 4/3/2019 Accepted for publication on: 6/3/2019 Abstract A survey of mite fauna inhabiting citrus orchards in Abutig, Assiut Gover- norate, yielded the discovery of a new species, Heterodispus longisetae n. sp. (Acari: Scutacaridae). The new species is morphologically described and illus- trated. Keywords: Acari, Heterostigmata, Scutacaridae, Heterodispus, citrus, Egypt. Introduction and Ebermann, 2012), however, the Mites of the family Scutacaridae genera Archidispus, Imparipes and Oudemans, 1916 (Acari: Trombidi- Pygmodispus have never been re- formes: Heterostigmatina) inhabit corded from Egypt. The genus Het- soil, forest litter, decomposing or- erodispus Paoli, 1911 is worldwide in ganic substrates, moss and manure. distribution and consists of 35 spe- They are also associated with various cies, eight of them are described from arthropods including ants, bees, flies, Egypt, namely: Heterodispus elonga- beetles and arachnids (Metwali, 1984; tus Trägårdh, 1905, H. adrosii Met- Momen, 1989; Khaustov and Chydy- wali, 1984, H. aegyptensis Momen & drov, 2004; Khaustov, 2008), while El-Bagoury, 1989, H. aegyptiacus some species are fungivorous Sevastianov and Abo-Korah, 1985, (Khaustov, 2008; Jagersbacher- H. evansi Momen & El-Bagoury, Baumann and Ebermann, 2012). This 1989, H. osmani Sevastianov and family consists of 24 genera and Abo-Korah, 1985, H. rackae Met- more than 800 species (Zhang, 2011). wali, 1984 and H. youssefi Metwali, The genus Archidispus Karafiat, 1959 1984. Paoli (1911) established Het- contains about 70 described species erodispus as a new subgenus of Im- that are mostly associated with bee- paripes Berlese using H. elongatus as tles of the family Carabidae (Kurosa, type species. The present work de- 1980; Khaustov, 2008). Distinct fe- scribes a new species of Heterodispus male dimorphism has been known in from soil of citrus in Egypt. various scutacarids including species Materials and Methods of the genus Archidispus. Some spe- Samples of leaf litter and soil cies are phoretic and showing specific under citrus trees were collected from characters suitable for such behavior different localities in Abutig at Assiut (Ebermann, 1991, 1999). governorate. Mites were extracted Until now, two scutacarid gen- using Tullgren funnels and preserved era Heterodispus and Scutacarus in 70% ethyl alcohol. The collected have been reported in Egypt (Met- specimens were cleared in lactic acid, wali, 1984; Jagersbacher-Baumann mounted in Hoyer's medium on glass Doi: 10.21608/ajas.2019.41245 Eraky, et al., 2019 http://ajas.journals.ekb.eg/ slides, dried on a hot plate, ringed weakly developed while apodemes with nail polish and examined under IV very short and joined with post- a phase-contrast microscope (BH-2®, sternal apodeme. Apodemes V ab- Olympus, Japan). Measurements in sent. All ventral setae thick, serrated micrometers (µm) were taken with a and sharply pointed; setae 1a the graded eyepiece and illustrations shortest and 4b the longest. Setae 4b were made using a drawing tube at- inserted anteriorly of 4a, however, tached to the microscope. The termi- positions of insertions of setae 4a and nology and setal nomenclature used 4b quite variable among paratypes. in the description were according to Posterior margin of ventral metapo- Lindquist (1986). The voucher slide- dosomal plate convex. Pseudanal se- mounted samples were deposited in tae finely serrated; setae ps1 visibly the Acari collection, Plant Protection longer and thicker than ps2 and ps3. Department, Faculty of Agriculture, Setal lengths: 1a 27, 1b 29, 2a 28, 2b Assiut University, Egypt (FAAU). 38, 3a 77, 3b 63, 3c 55, 4a 65, 4b 89, Results and Discussion 4c 57 µm. Distances between bases Cohort Heterostigmatina of setae: 1a–1a 29, 1b–1b 44, 2a–2a Superfamily Pygmephoroidea Cross, 35, 2b–2b 39, 3a–3a 15, 3b–3b 35, 1965 3c–3c 66, 4a–4a 28, 4b–4b 49, 4c–4c Family Scutacaridae Oudemans, 1916 63 µm. Genus Heterodispus Paoli, 1911 Legs (Figures 3 & 4). Setations Heterodispus longisetae n. sp. of legs I (solenidia in parenthesis): (Figures 1−4) Tr1–Fe3–Ge4–Ti4–Ts15 or 16(4). Female (holotype). Idiosomal Tarsus I (Figure 3) with distinct length 230 µm, width 172 µm; body sickle-like claw. Solenidion ω1 long oval to elongate. Dorsum (Figure 1). and finger-shaped, ω2, φ1 and φ2 Free margin of tergite C with marked smaller and thinner. Leg IV (Figure stripes; all dorsal setae finely serrated 4): Tr1-Fe2-Ge1-Ti3-Ts4. Trochanter and sharply pointed. Setae c1 and c2 with posteroventral axe-like projec- well developed and without alveoli. tion. Tarsus with long pretarsus and Cupules ia (tergite D) and ih (tergite minute empodium distally. H) small and oval. Setae h1 and h2 Males and larvae unknown. distinctly long. Length of dorsal se- Type material tae: c1 37, c2 34, d 40, e 35, f 37, h1 Holotype and paratype females 43, h2 40 µm. Distances between were collected from leaf litter under bases of setae: c1–c1 67, d–d 71, f–f mandarin; Abutig, Assiut, Egypt; 23 50, h1–h1 20, h2–h2 56 µm. Posterior February 2015; leg. A.S. Abdelgayed. margin of tergites C, D and EF Type materials are deposited in the smooth. Body surface finely stippled, Plant Protection Department, Faculty anterior margin of tergite C with fine, of Agriculture, Assiut University, longitudinal stripes. Egypt (FAAU). Venter (Figure 2). Apodemes I, Remarks II and sejugal apodeme (v-shaped) The genus Heterodispus com- well developed and merged with prises two subgenera, Heterodispus presternal apodeme. Apodemes III Paoli, 1911 and Teherodispus Ma- 201 Assiut J. Agric. Sci., (50) No. (2) 2019 (200-205) ISSN: 1110-0486 Website: www.aun.edu.eg/faculty_agriculture/journals_issues_form.php E-mail: [email protected] hunka, 1974 (Mahunka, 1977). Com- alveoli indistinct vs. simple and set monly, Heterodispus species have on distinct alveoli in H. chanti, (ii) setae c1 and c2 set on the outer free ventral setae sharply pointed vs. margin of clypeus but with few ex- blunt-ended in H. chanti and (iii) op- ceptions as in H. curryi Momen, 1989 isthosomal setae longer in the new and H. (T.) konrathi Mahunka, 1974 species than in H. chanti. setae cl arise behind the clypeus. The Etymology new species is very close to H. chanti The species epithet longisetae Soliman & Kandeel (in Zaher, 1986), refers to the distinctly long dorsal and however, it can be distinguished in ventral setae. having: (i) dorsal setae serrated and Figures 1-4. Heterodispus longisetae n. sp. Female. 1. Dorsal view; 2. Ventral view; 3. Tibia and tarsus of leg I; 4. Leg IV. 202 Doi: 10.21608/ajas.2019.41245 Eraky, et al., 2019 http://ajas.journals.ekb.eg/ Acknowledgment kyo: Zenkoku Noson Kyoiku Kyo- The authors are grateful to Prof. kai, 214–241. Dr. M.M. Kandeel (Faculty of Tech- Lindquist, E.E. 1986. The world genera nology and Development, Zagazig of Tarsonemidae (Acari: Het- University, Egypt) for confirmation erostigmata): a morphological, of the species identification. phylogenetic, and systematic revi- sion, with a reclassification of fam- References ily-group taxa in the Heterostig- Cross, E.A. 1965. The generic relation- mata. Memoirs of the Entomologi- ships of the family Pyemotidae cal Society of Canada, 118: 1–517. (Acarina: Trombidiformes). Univ. Mahunka, S. 1974. Auf Insekten le- Kansas Sci. Bull., 45: 29–275. benden Milben (Acari: Acarida, Ebermann, E. 1991. Das Phanomen Po- Tarsonemidae) aus Afrika. III. lymorphismus in der Milbenfami- Acta Zool. hung., 20: 367–402. lie Scutacaridae (Acari, Het- Mahunka, S. 1977. Beitrage zur erostigmata, Tarsonemina, Scuta- Kenntnis der Sistematik, Taxono- caridae). Zoologica, 141: 76 pp. mie, Ontogenie, Okologie und Ebermann, E. 1999. Kommentar zu den Verbreitung der Tarsonemiden. III. Schildchenmilben Kärntens (Acari: Folia. Ent. Hung., 30 (1): 85–97. Heterostigmata: Tarsonemini: Scu- Metwali, S.H. 1984. Survey on the fam- tacaridae). Naturschutz in Kärnten, ily Scutacaridae (Acari) in Egypt 15: 543–546. III. Acarologia, 25 (4): 323–328. Jagersbacher-Baumann, J. and Eber- Momen, F.M. 1989. Heterodispus curryi mann, E. 2012. Fungal spore trans- sp. n. a new scutacarid species fer and intraspecific variability of a (Acari: Tarsonemina) from Ireland. newly described African soil mite Acarologia, 30 (4): 361–363. (Heterostigmata, Scutacaridae, Momen, F.M. and El-Bagoury, M.E. Heterodispus). Zoologischer An- 1989. Five new species of scuta- zeiger, 251 (2): 101–114. carid mites (Acari: Tarsonemina) Karafiat, H. 1959. Systematik und Öko- from Egypt. Acarologia, 30 (1): logie der Scutacariden. Beiträge 41–50. zur Systematik und Ökologie mit- Oudemans, A.C. 1916. Acarologische teleuropäischen. Acarina, 1: 627– Aanteekeningen LIX. Entomolo- 712. gische Berichten, 4: 296–299. Khaustov, A.A. 2008. Mites of the fam- Paoli, G. 1911. Monografia dei tarsone- ily Scutacaridae of Eastern Palae- midi. Redia, 7: 215–281. arctic. Kiev (Ukraine): Akadempe- Sevastianov, V.D. and Abo-Korah, S.M. riodyka, 291 pp. 1985. New species of the family Khaustov, A.A. and Chydydrov, P.R. Scutacaridae (Tarsonemina: Trom- 2004. New species of mites of the bidiformes) from soil of agrocoe- family Scutacaridae (Acari: Het- noses in Egypt. Zool. Z., 64 (2): erostigmata) associated with ants 226–233. (In Russian). (Hymenoptera, Formicidae) from Trägårdh, I. 1905. Acariden aus Ägypten Turkmenistan. Acarina, 12 (2): 87– und dem Sudan. Zugleich ein Bei- 103. trag zur Kenntnis der Entwick- Kurosa, K. 1980. Caraboacaridae, Pyg- lungsgeschichte der Gattungen mephoridae, Scutacaridae.
Recommended publications
  • Two New Species of the Genus Elattoma (Acari: Heterostigmatina: Pygmephoridae) Phoretic on Morimus Verecundus (Coleoptera: Cerambycidae) from Iran
    Zootaxa 2903: 48–56 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Two new species of the genus Elattoma (Acari: Heterostigmatina: Pygmephoridae) phoretic on Morimus verecundus (Coleoptera: Cerambycidae) from Iran VAHID RAHIMINEJAD, HAMIDREZA HAJIQANBAR1 & YAGHOUB FATHIPOUR Department of Entomology, Faculty of Agriculture, Tarbiat Modares University, 14115-336, Tehran, Iran 1Corresponding author. E-mail: [email protected] Abstract Two new species of the genus Elattoma Mahunka, 1969 (Acari: Heterostigmatina: Pygmephoridae) associated with Mo- rimus verecundus (Faldermann 1836) (Coleoptera: Cerambycidae) are described and illustrated from Oak forests in Golestan province, Northern Iran: Elattoma cerambycidum Rahiminejad & Hajiqanbar sp. nov. and E. abeskoun Ra- himinejad & Hajiqanbar sp. nov. Both formed large colonies attached on the ventral surface, around coxae I–III of differ- ent individuals of the host beetles. This is the first phoretic record of the genus Elattoma for beetles of the family Cerambycidae. Furthermore, our record of Elattoma is new for the arthropod fauna of Iran. A key to world species of the genus Elattoma is also provided. Key words: Prostigmata, mite, beetle, phoretic relationship, Scolytidae, Iran Introduction Adult females of the family Pygmephoridae (Acari: Prostigmata: Heterostigmatina) generally utilize various insects for phoretic dispersal. These mites, including the genus Elattoma Mahunka, 1969, are usually free-living and fungivorous (Kaliszewski et al. 1995). Heretofore, the members of the genus Elattoma comprised eight species and had phoretic relationships most frequently with bark beetles (Scolytidae) and rarely with scarabaeids (Scara- baeidae) (Cross & Moser 1971; Khaustov 2000, 2003; Rodrigues et al. 2001).
    [Show full text]
  • Tiny Mites on a Great Journey a Review On
    Acarologia A quarterly journal of acarology, since 1959 Publishing on all aspects of the Acari All information: http://www1.montpellier.inra.fr/CBGP/acarologia/ [email protected] Acarologia is proudly non-profit, with no page charges and free open access Please help us maintain this system by encouraging your institutes to subscribe to the print version of the journal and by sending us your high quality research on the Acari. Subscriptions: Year 2019 (Volume 59): 450 € http://www1.montpellier.inra.fr/CBGP/acarologia/subscribe.php Previous volumes (2010-2017): 250 € / year (4 issues) Acarologia, CBGP, CS 30016, 34988 MONTFERRIER-sur-LEZ Cedex, France ISSN 0044-586X (print), ISSN 2107-7207 (electronic) The digitalization of Acarologia papers prior to 2000 was supported by Agropolis Fondation under the reference ID 1500-024 through the « Investissements d’avenir » programme (Labex Agro: ANR-10-LABX-0001-01) Acarologia is under free license and distributed under the terms of the Creative Commons-BY-NC-ND which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. Tiny mites on a great journey – a review on scutacarid mites as phoronts and inquilines (Heterostigmatina, Pygmephoroidea, Scutacaridae) Julia Baumanna a Institute of Biology, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. ABSTRACT The members of the family Scutacaridae (Acari, Heterostigmatina, Pygmephoroidea) are soil-living, fungivorous mites, and some of them are known to be associated with other animals. After reviewing the mites’ behavioural and morphological adaptations to their animal-associated lifestyle, the present publication shows the result of a thorough literature research on scutacarids living in different kinds of associations with other animal taxa.
    [Show full text]
  • Cryptic Speciation in the Acari: a Function of Species Lifestyles Or Our Ability to Separate Species?
    Exp Appl Acarol DOI 10.1007/s10493-015-9954-8 REVIEW PAPER Cryptic speciation in the Acari: a function of species lifestyles or our ability to separate species? 1 2 Anna Skoracka • Sara Magalha˜es • 3 4 Brian G. Rector • Lechosław Kuczyn´ski Received: 10 March 2015 / Accepted: 19 July 2015 Ó The Author(s) 2015. This article is published with open access at Springerlink.com Abstract There are approximately 55,000 described Acari species, accounting for almost half of all known Arachnida species, but total estimated Acari diversity is reckoned to be far greater. One important source of currently hidden Acari diversity is cryptic speciation, which poses challenges to taxonomists documenting biodiversity assessment as well as to researchers in medicine and agriculture. In this review, we revisit the subject of biodi- versity in the Acari and investigate what is currently known about cryptic species within this group. Based on a thorough literature search, we show that the probability of occur- rence of cryptic species is mainly related to the number of attempts made to detect them. The use of, both, DNA tools and bioassays significantly increased the probability of cryptic species detection. We did not confirm the generally-accepted idea that species lifestyle (i.e. free-living vs. symbiotic) affects the number of cryptic species. To increase detection of cryptic lineages and to understand the processes leading to cryptic speciation in Acari, integrative approaches including multivariate morphometrics, molecular tools, crossing, ecological assays, intensive sampling, and experimental evolution are recommended. We conclude that there is a demonstrable need for future investigations focusing on potentially hidden mite and tick species and addressing evolutionary mechanisms behind cryptic speciation within Acari.
    [Show full text]
  • Coleoptera: Scarabaeidae) from Iran
    Acta Zoologica Academiae Scientiarum Hungaricae 61(1), pp. 25–32, 2015 DOI: 10.17109/AZH.61.1.25.2015 TWO HETEROSTIGMATIC MITE SPECIES (ACARI: DOLICHOCYBIDAE, PODAPOLIPIDAE) ASSOCIATED WITH SCARABAEUS PI US (COLEOPTERA: SCARABAEIDAE) FROM IRAN Bahramian, M., Hajiqanbar, H.* and Talebi, A. A. Department of Entomology, Faculty of Agriculture, Tarbiat Modares University 14115-336, Tehran, Iran. E-mails: [email protected], [email protected] and [email protected]; *Corresponding author During a study on insect-associated heterostigmatic mites (Acari: Prostigmata) in southern Isfahan Province, Central Iran, two colonies of mites were found on Scarabaeus pius (Il- liger, 1803) (Coleoptera: Scarabaeidae): Pavania lanceolata sp. n. Bahramian et Hajiqanbar (Dolichocybidae) that is easily discernible by some modified foliate setae on tarsi I–III; and Tarsopolipus massai Husband, 1989 (Podapolipidae) for which Scarabaeus pius is a new host record. Key words: Heterostigmatina, Pavania, Tarsopolipus, new species, host record. INTRODUCTION Beetles of the superfamily Scarabaeoidea are one of the most typical co- leopterans, and even insects, to carry various kinds of mites. The mites from groups Mesostigmata, Prostigmata and Astigmatina encompass representa- tives associated with these beetles (e.g. Masan & Halliday 2009, Costa 1963, Oconnor 1982, Houck & Oconnor 1991, Bochkov & Klimov 2005, Kaliszews- ki et al. 1995). In Prostigmata, some heterostigmatic families such as Dolicho- cybidae (Hajiqanbar & Khaustov 2010), Scutacaridae (Ebermann et al. 2003), Pygmephoridae (Khaustov & Trach 2012), Microdispidae (Hajiqanbar et al. 2012) and Podapolipidae (Husband 1989) include species that have relation- ships with this group of beetles. Some mentioned families have only pho- retic relationship with scarab beetles (like Dolichocybidae, Pygmephoridae and Scutacaridae) however, some others are parasite of their hosts (like Po- dapolipidae).
    [Show full text]
  • Three New Species of the Genus Caesarodispus (Acari: Microdispidae) Associated with Ants (Hymenoptera: Formicidae), with a Key to Species
    bs_bs_banner Entomological Science (2015) 18, 461–469 doi:10.1111/ens.12149 ORIGINAL ARTICLE Three new species of the genus Caesarodispus (Acari: Microdispidae) associated with ants (Hymenoptera: Formicidae), with a key to species Vahid RAHIMINEJAD, Hamidreza HAJIQANBAR and Ali Asghar TALEBI Department of Entomology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran Abstract Three new species of the genus Caesarodispus (Acari: Heterostigmatina: Microdispidae) phoretic on ants are described from Iran: C. khaustovi Rahiminejad & Hajiqanbar sp. nov., C. pheidolei Rahiminejad & Hajiqanbar sp. nov. and C. nodijensis Rahiminejad & Hajiqanbar sp. nov. All species were associated with alate ants of the subfamily Myrmicinae (Hymenoptera: Formicidae) from northern Iran. A key to all species of Caesarodispus is provided. Key words: Heterostigmatina, host range, Iran, mite, phoresy. INTRODUCTION (Kaliszewski et al. 1995; Walter et al. 2009). The most prevalent hosts for this family are beetles and ants. Phoresy is a common form of migration in mites and, in Specific relationships between phoretic microdispid myrmecophilous species, phoresy usually occurs on mites and their phoronts are generally restricted to one alate ants (Hymenoptera: Formicidae) (Hermann et al. family or a few host genera: for instance, all mites of the 1970). At least 17 families of mites are associated genus Caesarodispus Mahunka, 1977 are associated with ants, the most common being the uropodine fami- with ants of the genera Myrmica, Messor, Tetramorium, lies
    [Show full text]
  • A Transitional Fossil Mite (Astigmata: Levantoglyphidae Fam. N.) from the Early Cretaceous Suggests Gradual Evolution of Phoresy‑Related Metamorphosis Pavel B
    www.nature.com/scientificreports OPEN A transitional fossil mite (Astigmata: Levantoglyphidae fam. n.) from the early Cretaceous suggests gradual evolution of phoresy‑related metamorphosis Pavel B. Klimov1,2*, Dmitry D. Vorontsov3, Dany Azar4, Ekaterina A. Sidorchuk1,5, Henk R. Braig2, Alexander A. Khaustov1 & Andrey V. Tolstikov1 Metamorphosis is a key innovation allowing the same species to inhabit diferent environments and accomplish diferent functions, leading to evolutionary success in many animal groups. Astigmata is a megadiverse lineage of mites that expanded into a great number of habitats via associations with invertebrate and vertebrate hosts (human associates include stored food mites, house dust mites, and scabies). The evolutionary success of Astigmata is linked to phoresy‑related metamorphosis, namely the origin of the heteromorphic deutonymph, which is highly specialized for phoresy (dispersal on hosts). The origin of this instar is enigmatic since it is morphologically divergent and no intermediate forms are known. Here we describe the heteromorphic deutonymph of Levantoglyphus sidorchukae n. gen. and sp. (Levantoglyphidae fam. n.) from early Cretaceous amber of Lebanon (129 Ma), which displays a transitional morphology. It is similar to extant phoretic deutonymphs in its modifcations for phoresy but has the masticatory system and other parts of the gnathosoma well‑ developed. These aspects point to a gradual evolution of the astigmatid heteromorphic morphology and metamorphosis. The presence of well‑developed presumably host‑seeking sensory elements on the gnathosoma suggests that the deutonymph was not feeding either during phoretic or pre‑ or postphoretic periods. Te evolution of metamorphosis is thought to have generated an incredible diversity of organisms, allowing them to exploit diferent habitats and perform diferent functions at diferent life stages1–5.
    [Show full text]
  • The Acari Very Small but Impossible to Deny!
    The Acari very small but impossible to deny! Scientific Programme http://www.acarology.org/ica/ica2018/ Turizm Organizasyon Yayıncılık Ltd. Şti. 1st DAY – 3 September 2018 (MONDAY) 10:00-10:45 Opening ceremony Sebahat K. Ozman-Sullivan – President, XV ICA 2018 Ferit Turanli – President, Entomological Society of Turkey Peter Schausberger-Secretary, Executive Committee, ICA: Remembrance of lost colleagues Zhi-Qiang Zhang – President, Systematic and Applied Acarology Society: James Allen McMurtry Awards 10:45-11:00 Coffee break 11:00-11:40 Keynote speaker / Fatih Sultan Mehmet Maria NAVAJAS Mites in a changing world 11:40-11:50 Presentations to sponsors 11:50-12:30 Keynote speaker / Fatih Sultan Mehmet Kosta Y. MUMCUOGLU The influence of global warming on tick vectors 12:30-14:00 Lunch Section 1. SYMPOSIUM: Parasitic and free living mites of medical and Section 1. Ecology and Section 1. Taxonomy and veterinary importance behavior of mites systematics Section 1. 1. Mites of medical importance Room Osman Gazi Fatih Sultan Mehmet Kanuni Sultan Suleyman Kosta Y. MUMCUOGLU Norman FASHING Tetsuo GOTOH Chairs Aysegul TAYLAN-OZKAN Rostislav ZEMEK Qing-Hai FAN Mites of the family Parasitidae Humidity perception in four Different strokes for astigmatid mite species Oudemans, 1901 (Acari: different folks: Strategies Mesostigmata) from Elena GAGNARLI, Franca evolved by two related Japan: a new species of 14.00-14.15 TARCHI, Neri ORSI BATTAGLINI, species in adapting to a Vulgarogamasus Tichomirov, Donatella GOGGIOLI, Silvia similar habitat 1969, and a key to species GUIDI, Laura SALVINI, Cristina Mohamed W. NEGM, Tetsuo TINTI, Sauro SIMONI Norman J. FASHING GOTOH Bibliometric analysis of Spider mites of the Balkan Intra- and transgenerational publications on house dust Peninsula: a review, new effects in generalist and mites records and recent outbreaks Emre DEMIR, Djursun specialist predatory mites 14.15-14.30 Ivana MARIĆ, Stanislav KARASARTOVA, Ayşe induced by prey limitation TRDAN, Tanja BOHINC, SEMRA GÜRESER, Kosta Andreas WALZER, Peter Snježana HRNČIĆ, Sanja Y.
    [Show full text]
  • A Review on Scutacarid Mites As Phoronts and Inquilines (Heterostigmatina, Pygmephoroidea, Scutacaridae) Julia Baumann
    Tiny mites on a great journey – a review on scutacarid mites as phoronts and inquilines (Heterostigmatina, Pygmephoroidea, Scutacaridae) Julia Baumann To cite this version: Julia Baumann. Tiny mites on a great journey – a review on scutacarid mites as phoronts and inquilines (Heterostigmatina, Pygmephoroidea, Scutacaridae). Acarologia, Acarologia, 2018, 58 (1), pp.192-251. 10.24349/acarologia/20184238. hal-01702711 HAL Id: hal-01702711 https://hal.archives-ouvertes.fr/hal-01702711 Submitted on 7 Feb 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - NoDerivatives| 4.0 International License Acarologia A quarterly journal of acarology, since 1959 Publishing on all aspects of the Acari All information: http://www1.montpellier.inra.fr/CBGP/acarologia/ [email protected] Acarologia is proudly non-profit, with no page charges and free open access Please help us maintain this system by encouraging your institutes to subscribe to the print version of the journal and by sending us your high quality
    [Show full text]
  • Actinedida No
    18 (3) · 2018 Russell, D. & K. Franke Actinedida No. 17 ................................................................................................................................................................................... 1 – 28 Acarological literature .................................................................................................................................................... 2 Publications 2018 ........................................................................................................................................................................................... 2 Publications 2017 ........................................................................................................................................................................................... 9 Publications, additions 2016 ........................................................................................................................................................................ 17 Publications, additions 2015 ....................................................................................................................................................................... 18 Publications, additions 2014 ....................................................................................................................................................................... 18 Publications, additions 2013 ......................................................................................................................................................................
    [Show full text]
  • Beaulieu, F., W. Knee, V. Nowell, M. Schwarzfeld, Z. Lindo, V.M. Behan
    A peer-reviewed open-access journal ZooKeys 819: 77–168 (2019) Acari of Canada 77 doi: 10.3897/zookeys.819.28307 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Acari of Canada Frédéric Beaulieu1, Wayne Knee1, Victoria Nowell1, Marla Schwarzfeld1, Zoë Lindo2, Valerie M. Behan‑Pelletier1, Lisa Lumley3, Monica R. Young4, Ian Smith1, Heather C. Proctor5, Sergei V. Mironov6, Terry D. Galloway7, David E. Walter8,9, Evert E. Lindquist1 1 Canadian National Collection of Insects, Arachnids and Nematodes, Agriculture and Agri-Food Canada, Otta- wa, Ontario, K1A 0C6, Canada 2 Department of Biology, Western University, 1151 Richmond Street, London, Ontario, N6A 5B7, Canada 3 Royal Alberta Museum, Edmonton, Alberta, T5J 0G2, Canada 4 Centre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, N1G 2W1, Canada 5 Department of Biological Sciences, University of Alberta, Edmonton, Alberta, T6G 2E9, Canada 6 Department of Parasitology, Zoological Institute of the Russian Academy of Sciences, Universitetskaya embankment 1, Saint Petersburg 199034, Russia 7 Department of Entomology, University of Manitoba, Winnipeg, Manitoba, R3T 2N2, Canada 8 University of Sunshine Coast, Sippy Downs, 4556, Queensland, Australia 9 Queensland Museum, South Brisbane, 4101, Queensland, Australia Corresponding author: Frédéric Beaulieu ([email protected]) Academic editor: D. Langor | Received 11 July 2018 | Accepted 27 September 2018 | Published 24 January 2019 http://zoobank.org/652E4B39-E719-4C0B-8325-B3AC7A889351 Citation: Beaulieu F, Knee W, Nowell V, Schwarzfeld M, Lindo Z, Behan‑Pelletier VM, Lumley L, Young MR, Smith I, Proctor HC, Mironov SV, Galloway TD, Walter DE, Lindquist EE (2019) Acari of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment.
    [Show full text]
  • Thanatosis and Morphological Adaptations in the Mite Genera Lamnacarus and Pygmodispus (Acari, Heterostigmatina, Scutacaridae)
    S O I L O R G A N I S M S Volume 84 (2) 2012 pp. 471–479 ISSN: 1864-6417 Thanatosis and morphological adaptations in the mite genera Lamnacarus and Pygmodispus (Acari, Heterostigmatina, Scutacaridae) Julia Jagersbacher-Baumann and Ernst Ebermann* Institut für Zoologie, Karl-Franzens-Universität Graz, Universitätsplatz 2, 8010 Graz, Austria *Corresponding author. Ernst Ebermann (e-mail: [email protected]) Abstract In the mite family Scutacaridae, several species belonging to different genera show thanatosis or ‘playing dead’ behaviour. Some of them possess morphological features that are obviously connected with this behaviour. We compared the morphological adaptations to thanatosis in females of Lamnacarus ornatus Balogh and Mahunka, 1963 to those in Pygmodispus (Allodispus) pavidus Ebermann, 1997. To exhibit no point of attack to predators, the mites must retract their legs and cover them with adapted structures. Although the principles of the morphological adaptations to thanatosis are similar in P. (A.) pavidus and L. ornatus, there are differences in their completion. Keywords: Thanatosis, morphological adaptations, Scutacaridae, Pygmodispus pavidus, Lamnacarus ornatus 1. Introduction Thanatosis or ‘playing dead’ behaviour is a common reaction of mites to predator pressure. It is displayed by animals that are armoured with strongly sclerotised cuticular structures. Often, morphological adaptations are established that allow the withdrawal of the legs, which are supposed to be the most vulnerable body parts. Ebermann (1991a) described thanatosis and the corresponding morphological features in the mite family Scutacaridae, focusing on the females of Pygmodispus (Allodispus) pavidus Ebermann, 1997. The morphological adaptations of females of Lamnacarus ornatus Balogh and Mahunka, 1963 to thanatosis are described by Ebermann as being extremely similar, although the two genera are only distantly related.
    [Show full text]
  • A Summary List of Fossil Spiders and Their Relatives Compiled By
    A summary list of fossil spiders and their relatives compiled by Jason A. Dunlop (Berlin), David Penney (Manchester) & Denise Jekel (Berlin) with additional contributions from Lyall I. Anderson, Simon J. Braddy, James C. Lamsdell, Paul A. Selden & O. Erik Tetlie 1 A summary list of fossil spiders and their relatives compiled by Jason A. Dunlop (Berlin), David Penney (Manchester) & Denise Jekel (Berlin) with additional contributions from Lyall I. Anderson, Christian Bartel, Simon J. Braddy, James C. Lamsdell, Paul A. Selden & O. Erik Tetlie Suggested citation: Dunlop, J. A., Penney, D. & Jekel, D. 2017. A summary list of fossil spiders and their relatives. In World Spider Catalog. Natural History Museum Bern, online at http://wsc.nmbe.ch, version 18.0, accessed on {date of access}. Last updated: 04.01.2017 INTRODUCTION Fossil spiders have not been fully cataloged since Bonnet’s Bibliographia Araneorum and are not included in the current World Spider Catalog. Since Bonnet’s time there has been considerable progress in our understanding of the fossil record of spiders – and other arachnids – and numerous new taxa have been described. For an overview see Dunlop & Penney (2012). Spiders remain the single largest fossil group, but our aim here is to offer a summary list of all fossil Chelicerata in their current systematic position; as a first step towards the eventual goal of combining fossil and Recent data within a single arachnological resource. To integrate our data as smoothly as possible with standards used for living spiders, our list for Araneae follows the names and sequence of families adopted in the previous Platnick Catalog.
    [Show full text]