2012-11-05

J. Acarol. Soc. Jpn., 21(2): 141-146. November 25, 2012 © The Acarological Society of Japan http://acari.ac.affrc.go.jp/ 141

One new of the genus Sternostoma (: ) from Cuculus canorus (Cuculiformes: Cuculidae) from Leningrad Province, Russia

1 2 Ivan DIMOV * and Wayne KNEE

1Laboratory of Parasitology, Zoological Institute, Russian Academy of Science, Universitetskaya embankment 1, Saint Petersburg, 199034, Russia 2Canadian National Collection of , and Nematodes, Agriculture and Agri-Food Canada, 960 Carling ave., K.W. Neatby bldg. Ottawa, Ontario, K1A 0C6, Canada. (Received 18 September 2012; Accepted 3 October 2012)

ABSTRACT

Birds are host to a wide assemblage of parasitic , including (), lice (Phiraptera) and fleas (Siphonaptera). A new species of nasal , Sternostoma zini n. sp. (Mesostigmata: Rhinonyssidae), collected from the Common , Cuculus canorus (Linnaeus, 1758) (Cuculiformes: Cuculidae) from Leningrad province, Russia, is described and illustrated. Sternostoma zini n. sp. is most similar to Sternostoma cuculorum Fain, 1956, which was also described from Cuculus canorus. These two species are distinguishable by several characteristics, such as the shape of the opisthosomal and genital shields, as well as opisthosomal and hypostomal chaetotaxy. Key words: Rhinonyssidae, Sternostoma zini, nasal mites, Cuculiformes, Cuculus canorus

INTRODUCTION

Mites (Arachnida: Acari) are one of the most diverse and common associates of , with at least 3,000 described species and 40 families of mites reported from birds (Proctor and Owens, 2000). The nature of symbioses between these mites and their hosts is variable, in that some species are highly detrimental parasites, such as the rhinonyssid nasal mite Sternostoma tracheacolum Lawrence, 1948, while others are commensal associates, such as most feather mites (Astigmata: , Pterolichoidea, Freyanoidea) (Proctor and Owens, 2000). Birds are host to at least 500 described species of nasal mites, with the rhinonyssids being the most frequently encountered group (Fain, 1994; Knee et al., 2008). Rhinonyssids are obligate haematophagous endoparasites of non-ratite birds; they reside primarily in the nasal turbinates, a scroll of blood-rich epithelial tissue, and occasionally in the trachea, lungs and body cavity of their hosts (Bell, 1996; Krantz, 1978; Porter and Strandtmann, 1952). Typically, these mites * Corresponding author: E-mail; [email protected] DOI: 10.2300/acari.21.141 2012-11-05

142 Ivan DIMOV and Wayne KNEE are not considered to cause significant pathology to their hosts; however, their feeding may cause trauma to the nasal tissues, and they may serve as reservoirs or vectors of disease-causing infectious agents (De-Rojas et al., 2002; Dimov, 2012a). The level of host specifi city is variable across rhinonyssid genera, in that some genera are restricted to one host family, while others occur on hosts from several avian orders (Butenko, 1984; Fain, 1994; Pence, 1975). Avian nasal mites have been surveyed in many countries, including the USA, Canada, Australia, Taiwan, and Russia (Butenko, 1984; Domrow, 1969; Knee et al., 2008; Maa and Kuo, 1965; Pence, 1975). At least 140 species of rhinonyssids have been collected from birds in Russia over the last 60 years (Dimov, 2012b); however, our understanding of Russian rhinonyssid fauna is largely incomplete. In an attempt to address this lack of knowledge, I.D. initiated a survey of the rhinonyssid fauna of birds in Leningrad province, Russia (Dimov, 2010). In Leningrad, a total of 18 species of rhinonyssids, from seven genera, have been collected from 42 species, representing eight orders (Dimov, 2012b). Throughout this survey, we discovered a new rhinonyssid species of the genus Sternostoma, collected from the , Cuculus canorus (Cuculiformes: Cuculidae). Herein we describe and illustrate this new species.

MATERIALS AND METHODS

Deceased Common Cuckoo specimens were collected by amateur ornithologists, Olga Sizmina and Anton Rubtsov. Mites were collected by dissecting the host’s nasal cavities, in which the head was placed in a glass dish, and the nasal cavities were dissected using scissors. Nasal cavities were examined for mites using a Leica ST 50 dissecting microscope. Mites were removed and preserved in 70% ethanol. Mites were cleared in 75% lactic acid for 2–4 hours, then washed in 70% ethanol for 2–3 minutes, and slide-mounted in Hoyer’s medium. Slide-mounted specimens were examined using a Leica DM4500 compound microscope and illustrated using a camera lucida, drawings were later edited using Adobe Photoshop 7.0. Species descriptions are based on the female holotype and one female paratype, and follow the format of Pence (1975) and Knee (2008). The following designations are adapted from Fain and Hyland (1962) and Knee (2008): LB, length of body including palps; WID, width of idiosoma; LPS, length of podosomal shield; WPS, width of podosomal shield; LOS, length of opisthosomal shield; WOS, width of opisthosomal shield; LSS, length of sternal shield; WSS, width of sternal shield; LGS, length of genital shield; WGS, width of genital shield; LG, length of gnathosoma, ventral view, including palps; WG, width of gnathosoma; Lleg I to Lleg IV, length of leg, including coxa, excluding ambulacrum. All measurements are in micrometers. Holotypes and paratypes are deposited in the Zoological Institute of the Russian Academy of Sciences collection in St. Petersburg, Russia (ZISP 4834, 4835).

RESULTS

Family Rhinonyssidae Trouessart, 1895 Genus Sternostoma Berlese and Trouessart, 1889 The genus Sternostoma is a species-rich genus with at least 60 described species (Butenko, 2012-11-05

One new species of the genus Sternostoma (Mesostigmata: Rhinonyssidae) from Cuculus canorus (Cuculiformes: Cuculidae) from Leningrad Province, Russia 143

1984; Fain, 1957; Knee et al., 2008). Sternostoma species have been collected from 18 orders of birds worldwide (Domrow, 1969). Herein we recognize and describe one new Sternostoma species. Sternostoma zini n. sp (Figs. 1–2)

DESCRIPTION

Female (based on holotype and 1 paratype): LB 630, 651; WID 317, 340; LPS 290, 300; WPS 310, 321; LOS 288; WOS 308, 320; LSS 150, 158; WSS 101, 106; LGS 132, 139; WGS 95, 101; LG 94, 99; WG 66, 72; Lleg I 370, 389; Lleg II 353, 360; Lleg III 330, 342; Lleg IV 340, 356.

Dorsum (Fig. 1): Podosomal shield lightly sclerotized with 19 short setae (j1-6, z2,4,6) on the

Fig. 1. Sternostoma zini n. sp. Dorsum. 2012-11-05

144 Ivan DIMOV and Wayne KNEE shield (in the holotype). In the paratype there are 20, with paired j4. Podosomal shield covering most part of the dorsal podosoma. Stigmata located dorsolaterally at a level of posterior margin of podosomal shield. Opisthosomal shield lightly sclerotized, nearly as long as wide, covering most of the dorsal opisthosoma. Opisthosomal shield with six pairs of short setae (J1-5, R1) and a pair of small pores near setae J3.

Venter (Fig. 2): Sternal shield poorly sclerotized, three pairs of short setae (St1,2,3) on the shield. Genital shield broad and poorly sclerotized, and its posterior margin subtriangular, with one pair of short setae (he 4) on posterolateral corner of the shield. Ventral opisthosoma with two pairs of large setae (Jv1,2), and one pair of short setae (Zv2) half as long as Jv1,2. Anal shield located on idiosomal posterior margin, with one pair of adanal setae at a level of anal opening. Gnathosoma inserted ventrally, hypostomal setae and deutosternal teeth absent. Legs: All legs six-segmented. Chaetotaxy of legs: Coxae 2-2-2-1; trochanters 3-4-4-4; femurs 8-5-4-4; genua 5-4-4-4; tibiae 6-5-5-5; tarsi 13-17-17-17. All tarsi with ambulacrum. Male, nymphs, larva: Unknown.

Fig. 2. Sternostoma zini n. sp. Venter. 2012-11-05

One new species of the genus Sternostoma (Mesostigmata: Rhinonyssidae) from Cuculus canorus (Cuculiformes: Cuculidae) from Leningrad Province, Russia 145

Type materials: Female holotype (ZISP 4834) and one female paratype (ZISP 4835) from Cuculus canorus (Linnaeus, 1758) (Cuculidae), Vyrica (59°24'N, 30°20'E), Leningrad province, Russia, 13 July 2010, coll. by I. Dimov. Etymology: The species is named after the Zoological Institute (ZIN) Russian Academy of Science in Saint Petersburg.

DISCUSSION

Sternostoma zini n. sp. is most similar to Sternostoma cuculorum, which was also collected from Cuculus canorus in Tyumen and Tomsk provinces in Russia (Butenko, 1984; Fain 1956, 1957). Several morphological characteristics can be used to delineate between S. zini and S. cuculorum Cuculus canorus is an obligate , and it lays eggs in the nests of over 125 species of birds (Skjelseth et al., 2004). Considering the parasitic life history of C. canorus, there is a possibility that Sternostoma zini n.sp. is also associated with the host birds of the common cuckoo, or that C. canorus shares the rhinonyssid fauna of its hosts. For example, Molothrus ater (Boddaert, 1783) (Passeriformes: Icteridae) is also an obligate brood parasite, and is associated with over 200 species of birds (Ortega, 1998). In Canada, two species of rhinonyssids were collected from M. ater, one species, icteridius (Strandtmann & Furman, 1956), is typically found on birds of the family Icteridae; while the other species, P. japuibensis Castro, 1948, is usually associated with species in families which M. ater parasitizes (Knee et al., 2008). In order to gain a better understanding of the ecology and host specifi city of S. zini n. sp. we need to survey the rhinonyssid fauna of the host birds of C. canorus

ACKNOWLEDGEMENTS

We are grateful to Olga Sizmina and Anton Rubtsov for providing us with bird specimens. We thank Sergey Mironov (Zoological Institute, Russian Academy of Science) for his advice and assistance with our research.

Table 1. Characters differentiating Sternostoma zini n.sp. and S. cuculorum

Character S. zini n. sp. S. cuculorum

Dorsal Opisthosomal seta R1 present absent

Ventral Opisthosomal seta Zv2 half as long as JV2 as long as JV2 Opisthosomal shield as long as wide twice as long as wide Posterior margin of genital shield subtriangular rounded Sternal shield poorly sclerotized well sclerotized Hypostomal setae absent present 2012-11-05

146 Ivan DIMOV and Wayne KNEE

REFERENCES

Bell, P. J. (1996) The life history and transmission biology of Sternostoma tracheacolum Lawrence (Acari: Rhinonyssidae) associated with the Gouldian fi nch Erythrura gouldiae. Experimental and Applied Acarology, 20: 323-341. Butenko, O. M. (1984) Rhinonyssid Mites of Non- Birds of the USSR. 188 p., Academy of Sciences of USSR, Moscow. De-Rojas, M., M. D. Mora, J. M. Ubeda, C. Cutillas, M. Navajas and D. C. Guevara. (2002) Phylogenetic relationships in rhinonyssid mites (Acari: Rhinonyssidae) based on ribosomal DNA sequences: insights for the discrimination of closely related species. Parasitology Research, 88: 675-681. Dimov, I. D. (2010) Rhinonyssid mites (: Gamasina) from nasal cavities of birds in the Leningrad province during the summer-autumnal seasons. International Journal of Veterinary, 4: 6-9. Dimov, I. D. (2012a) A new nasal mite of the genus Ptilonyssus (Rhinonyssidae) from Parus caeruleus (Passeriformes) from Russia. Journal of the Hellenic Veterinary Medical Society, 63: 25-29. Dimov, I. D. (2012b) Rhinonyssid mites (Gamasina: Rhinonyssidae) from birds of Leningrad region. Accounting scientific session following the results of works 2011. Theses of reports on April, 3-5 2012, pp. 12-13. Zoological Institute, Russian Academy of Science, St. Petersburg. Domrow, R. (1969) The nasal mites of Queensland birds (Acari: Dermanyssidae, Ereynetidae, and ). Proceedings of the Linnean Society of New South Wales, 93: 297- 426. Fain, A. (1956) Les acariens de la famille Rhinonyssidae Vitzthum 1935 parasites des fosses nasales des oiseaux au Ruanda-Urundi. Revue Zoologie et de Botanique. Africaines, 53 : 131-157. Fain, A. (1957) Les acariens des familles Epidermoptidae et Rhinonyssidae parasites des fosses nasales d’oiseaux au Ruanda-Urundi et au Congo Belge. Annales du Musée Royal du Congo Belge 60: 1-176. Fain, A. (1994) Adaptation, specificity and host parasite coevolution in mites (Acari). International Journal for Parasitology, 24: 1273-1283. Fain, A. and K. E. Hyland. (1962) The mites parasitic in the lungs of birds. The variability of Sternostoma tracheacolum Lawrence, 1948, in domestic and wild birds. Parasitology, 52: 401-424. Knee, W. (2008) Five new species of Rhinonyssidae (Mesostigmata) and one new species of Dermanyssus (Mesostigmata: Dermanyssidae) from birds of Alberta and Manitoba, Canada. Journal of Parasitology, 94: 348-374. Knee, W., H. Proctor and T. Galloway. (2008) Survey of nasal mites (Rhinonyssidae, Ereynetidae, and Turbinoptidae) associated with birds in Alberta and Manitoba, Canada. The Canadian Entomologist, 140: 364-379. Krantz, G. W. (1978) A Manual of Acarology, 2nd ed. 509 p., Oregon State University Book Stores, Corvallis, Oregon. Maa, T. C. and J. S. Kuo. (1965) A fi eld survey of parasites of birds in Taiwan. Journal of Medical Entomology, 1: 395-401. Ortega, C. P. (1998) Cowbirds and Other Brood Parasite. 371 p., University of Arizona Press, Tucson, Arizona. Pence, D. B. (1975) Keys, species and host list, and bibliography for nasal mites of North American birds (Acarina: Rhinonyssinae, Turbinoptinae, Speleognathinae, and Cytoditidae). Special Publications of the Museum of Texas Tech University, 8: 1-148. Porter, J. C. and R. W. Strandtmann. (1952) Nasal mites of the English sparrow. Texas Journal of Science, 4: 393-399. Proctor, H. C. and I. Owens. (2000) Mites and birds: diversity, and coevolution. Trends in Ecology and Evolution, 15: 358-364. Skjelseth, S., A. Moksnes, E. Røskaft, H. L. Gibbs, M. Taborsky, B. Taborsky, M. Honza and O. Kleven. (2004) Parentage and host preference in the common cuckoo Cuculus canorus. Journal of Avian Biology, 35: 21-24.