A total of 30 nests of
Parus major were collected in 2010 at the following 4 sites from Northeastern Bulgaria (Fig. 1):
(1)
Panitsovo (N 42°51’1.41” E 27°40’14.02”, 250 – 300 m a. s. l., 3 nests, No 1 – 3). The area is situated in the eastern part of Stara Planina Mts. The region is dominated by xerothermic grass vegetation:
Dichantium ischaemum and
Poa bulbosa. The mountain part is mostly covered by deciduous forests.
(2)
Provadia (N 43°12’12.24” E 27°26’38.06”, 52 m a. s. l., 4 nests, No 4 – 7). The nests are collected in the edge of the forest, within the boundaries of the city, consisting primarily of artificially planted parks and ornamental trees. Near the area are mixed deciduous forests with a significant predominance of
Quercus cerris,
Quercus frainetto,
Quercus polycarpa and
Carpinus betulus.
(3)
Albena (N 43°21’48.02” E 28°04’43.26”, 10 m a. s. l., 4 nests, No 8 – 11). The area is situated in the eastern part of Batova River, near the beach. It is covered with natural dense forest represented mainly of
Fraxinus oxycarpa,
Ulmus minor,
Quercus pedunculiflora,
Acer campestre,
Alnus glutinosa and swamp and marsh hygrophytic formations.
(4)
Goritsa (N 42°55’10.11” E 27°48’56.08’, 160 – 205 m a. s. l., 19 nests, No 12 – 30). Located in the eastern part of Kamchia Mountain. The main habitats are represented by mixed deciduous forests dominated by
Quercus cerris, Quercus frainetto, Quercus dalechampii, Fagus orientalis (Bondev 1991).
The nest material was collected from wooden nest boxes. Nests were picked up after the end of breeding and transported to a laboratory. The mites were extracted from the nests by means of Tulgren’s funells and
preserved in 75% ethanol. The collected specimens were mounted into slides in lactophenol and examined using a light microscope (Bloszyk et al. 2006).
Species identification was made according to
Bregetova (1956),
Till (1963),
Kontschán (2007),
Roy &
Chauve (2009) and
Roy et al. (2009).
For analysis of community structure of mites were used the following indices (according to
Margolis et al. 1982): prevalence (P%) (percentage of nests in which the species occurred); relative density (R) (ratio of the number of specimens of every species to the number of all nests); mean intensity (I) (ratio of the number of specimens of every species to the number of nests, in which the species was found) and dominance (D%) (ratio of the number of specimens of every species to the number of all the specimens, in percent). According to their dominance the species were divided into 5 groups: eudominant (> 10%); dominant (5 – 10%); subdominant (1 – 5%); recedent (0.5 – 1%), and subrecedent (< 0.5%).
|
Figure 1.
Location of study sites. |
|
A total of 912 specimens belonging to 16 species of order Parasitiformes were found in nests of
Parus major. The list of taxa and values of some indices of established mites in the studied sites are presented in Table 1.
Of the 30 nests examined, 25 or 83.33% were infested with mesostigmatic mites. No mites were found in 1 nest from Albena, 2 nests from Provadia and 2 nests from Goritsa. Eleven out of 16 identified species were found only in one of the sites surveyed. Fifteen or 93.8% of the species were established in nests from Goritsa. Only one species –
Androlaelaps casalis was found in all four areas studied (Table 1).
The number of species per one nest fluctuated between 1 and 7, the average number of mites per one nest was 1.87. Eleven or 44% of the nests where mesostigmatic mites were recorded were occupied only by one species. The highest number of species (7) was found in a single nest. The abundance of mites fluctuated between 1 and 154 specimens in one nest, the average abundance per one nest was 30.40 (Table 2).
The species
Androlaelaps fahrenholzi, Hypoaspis lubrica,
Laelaps agilis,
Hirstionyssus criceti,
Myonyssus decumani,
Myonyssus gigas,
Macrocheles
glaber and
Haemogamasus
nidi are reported for the first time in nests of birds in Bulgaria.
The most frequent species was
A. casalis presented in 23 nests, prevalence 76.67%. Other comparatively frequently occurring mites were
Dermanyssus gallinae (present in 7 or 23.33% of nests) and
Ornithonyssus sylviarum (present in 4 or 13.33% of nests). Other mite species were infested less than 10% of nests. There was no species established in all positive for gamaside mites nests (Table 1).
The highest dominance was recorded of
A. casalis again (83.00%). The ectoparasites
D. gallinae (4.50%) and
O. sylviarum (3.51%) as well as
H. lubrica (2.64%) and
M. glaber (1.86%) were established with a smaller number of specimens and belong to the subdominants. The remaining 11 species (or 68.75% of the observed species) were found with 1 – 9 specimens only and belong to the recedent and subrecedent.
Analysing the relative density and mean intensity of established species were received similar results – again the highest values
of these indices were observed in
A. casalis (32.91 and 25.23),
O. sylviarum (8.00 and 1.07) and D. gallinae (5.13 and 1.37). The species H. lubrica and
M. glaber had high mean intensity – 8.00 and 8.50 respectively, but low relative density – 0.80 and 0.57. In other species these values were much lower (Table 1).
The comparison of the abundance of widespread species in particular nests shows that
A. casalis appears eudominant in all nests in which it is found, as in 10 or 43.48% of them he has 100% dominance. However, the number of specimens with which it is established varies considerably – between 1 and 140 (Table 2). The blood-sucking mite
D. gallinae is eudominant in 5 and dominant in 3 of the nests and the number of specimens varies between 1 and 10.
O. sylviarum also present with a different number of specimens in individual nests (between 1 and 15), as in 3 of them it is eudominant and in 1 – subdominant. Similar results on the distribution of mesostigmatic mites are reported by
Mašán &
Stanko (2005). Investigating the nests of
Mus spicilegus authors indicate that abundance and dominance of the species markedly varied in individual nests, according to microhabitat condition at individual collection sites.
Only one mite –
A. casalis of the 5 eudominant and dominant species predominate in all four studied sites.
D. gallinae has a high relative significance in nests from three of sites – Provadia, Albena and Goritsa,
O. sylviarum – in two of them: Panitsovo and Goritsa, and
H. lubrica and
M. glaber were established in
Goritsa only.
|
Table 1.
Mesostigmatic mites (Parasitiformes) established in
nests of P. major. |
|
Table 2.
Abundance (N) and dominance (D) of the most frequent and
abundant Mesostigmata species in individual nests of
P. major.
|
|
Ambros M, Krištofík J & Šustek Z, 1992: The mites (Acari: Mesostigmata) in the birds’ nests in Slovakia.
Biologia,
Bratislava, 47: 369–381.
Bloszyk J, Bajerlein D, Gwiazdowicz D, Halliday R & Dylewska M, 2006: Uropodine mite communities (Acari: Mesostigmata) in birds’ nests in Poland.
Belg. J. Zool., 136 (2): 145–153.
Bloszyk J, Dražina T, Gwiazdovicz D, Halliday B, Goldyn B, Napierala A & Rybska E, 2011: Mesostigmatic mites (Acari: Mesostigmata) in nests of the Eurasian griffon vulture (Gyps fulvus) in Croatia.
Biologia,
Bratislava, 66/2: 335–339.
Bondev I, 1991: The vegetation of Bulgaria. Map of M 1:600000 with explanatory text.
Publishing House “St. Kliment Ohridski”, Sofia, 183 pp. [in Bulgarian]
Bregetova N, 1956: Gamasid mites (Gamasoidea).
Opred. Faune SSSR, 61, 247 pp.
Davidova R & Vasilev V, 2011: Gamasid mites (Acari, Mesostigmata) in the nest holes of three passerine species from Kamchia Mountain (Northeastern Bulgaria).
Sci Parasitol., 12 (4): 215–221.
Fenďa P, 2010: Mites (Mesostigmata) inhabiting bird nests in Slovakia (Western Carpathians), pp. 199–205. In:
Sabelis M & Bruin J (eds), Trends in Acarology. Proceedings of the 12th International Congress, 1st Edition, Springer Science + Business Media B.V.,
Dordrecht, Heidelberg, London, New York.
Fenďa P, Kucman P, Bačíková S, Országhová Z, Puchala P, Sobeková K, Jánošková V & Melišková M, 2011: The mites (Acari, Mesostigmata) in the nests of Tree Sparrow (Passer montanus) in Nature Reserve Šúr (SW Slovakia).
Folia faunistica Slovaca, 16 (1): 37–44.
Gajdoš P,
Krištofík J & Šustek Z, 1991: Spiders (Araneae) in the birds’ nests in Slovakia.
Biologia,
Bratislava, 46: 887–905.
Georgiev K &
Mitev I, 2007: Great tit
Parus major, pp. 548–549. In:
Iankov P (ed.), Atlas of Breeding Birds in Bulgaria. Bulgarian Society for the Protection of Birds, Conservation Series, Book 10, BSPB, Sofia.
Gwiazdowicz D, Mizera T & Skorupski M, 1999: Mites in greater spotted eagle nests.
Journal of Raptor Research, 3(3): 257–260.
Hicks E, 1959: Check-list and bibliography on the occurence of insects in bird nests.
Ames, Iowa, 681 pp.
Kontschán J, 2007: New and rare Mesostigmatid mites to the fauna of Hungary.
Folia Historico Naturalia Musei Matraensis 31: 99–106.
Koyumdjieva M, 1981: Gamasoid mites (Gamasoidea, Parasitiformes) from bird’s nests in Bulgaria.
Acta Zoologica Bulgarica 18: 78–80.
Krištofík J &
Mašán P, 1996: Population structure changes of Dermanyssus hirundinis and Ornithonyssus sylvarium (Acarina, Mesostigmata) in the penduline tit (Remiz pendulinus) nests during the breeding period.
Biologia, Bratislava, 51: 519–529.
Krištofík J,
Mašán P &
Šustek Z, 1996: Ectoparasites of bee-eater (Merops apiaster) and arthropods in its nests.
Biologia, Bratislava, 50: 557–570.
Krištofík J, Mašán P, Šustek Z & Gajdoš P, 1993: Arthropods in the nests of penduline tit (Remiz pendulinus). Biologia,
Bratislava, 48: 493–505.
Krištofík J, Mašán P, Šustek Z & Kloubec B, 2003: Arthropods (Pseudoscorpionidea, Acari, Coleoptera, Siphonaptera) in the nests of the tengmalm’s owl,
Aegolius funereus.
Biologia,
Bratislava, 58: 231–240.
Krištofík J, Mašán P & Šustek Z, 2005: Arthropods in the nests of marsh warblers (Acrocephalus palustris).
Biologia,
Bratislava, 60: 171–177.
Krištofík J, Mašán P & Šustek Z, 2007: Arthropods (Pseudoscorpionidea, Acarina, Coleoptera, Siphonaptera) in nests of the bearded tit (Panurus biarmicus).
Biologia,
Bratislava, 62/6: 749–755.
Madej G & Stañska M, 1999: Gamasid mites (Arachnida, Acari) in the nests of secondary hollow nesters Collared Flycatcher (Ficedula albicollis T.) and Pied Flycatcher (Ficedula hypoleuca P.) in the Bialowieza Forest.
Parki Nar. i Rez. Przyrody, 8: 35–39.
Margolis L, Esch G, Holmes J, Kuris A & Schad G, 1982: The use of ecological terms in parasitology (report of an ad hoc committee of the American Society of Parasitologists).
Journal of Parasitology, 68 (1): 131–133.
Mašán P &
Stanko M, 2005: Mesostigmatic mites (Acari) and fleas (Siphonaptera) associated with nests of mound-building mouse, Mus spicilegus Petényi, 1882 (Mammalia, Rodentia).
Acta Parasitologica, 3: 228–234.
Roy L & Chauve C, 2009: The genus Dermanyssus (Mesostigmata: Dermanyssidae): history and species characterization.
Trends in Acarology, 49–55.
Roy L, Dowling A, Chauve C & Buronfosse T, 2009: Delimiting species boundaries within
Dermanyssus Duges, 1834 (Acari: Dermanyssidae) using a total evidence approach.
Molecular Phylogenetics and Evolution, 50: 446–470.
Salmane I, 2001: A check-list of Latvian Gamasina mites (Acari, Mesostigmata) with short notes to their ecology.
Latvijas Entomologs, 38: 50–61.
Sokolova T & Lopatina Y, 2003: Parasitic dermatoses: scabies and mouse dermatitis.
Moscow, 120 pp. [in Russian]
Švaňa M, Fenďa P & Országhová Z, 2006: The mites (Acari: Mesostigmata) in the birds nests in SW Slovakia.
Folia faunistica Slovaca, 11 (7): 39–42.
Till W, 1963: Ethiopian mites of the genus Androlaelaps Berlese s. lat. (Acari: Mesostigmata).
Bulletin of the British Museum of Natural History (Zoology), 10 (1): 1–104.
Tryjanowski P, Baraniak E, Bajaczyk R, Gwiazdowicz D, Konwerski S, Olszanowski Z & Szymkowiak P, 2001: Arthropods in nests of the red-backed shrike (Lanius collurio) in Poland.
Belgian Journal of Zoology, 131 (1): 69–74.
Wasylik A, 1971: Nest types and abundance of mites.
Ekologia Polska, 19: 689–699.
Zhaksilikova R, 2006: The harmful importance of ticks for humans.
Medical parasitology and parasitic diseases, 2: 54–58.
|