Eva Tirjaková
Acta Protozoologica, Volume 56, Issue 2, 2017, pp. 77 - 91
https://doi.org/10.4467/16890027AP.17.007.7482Eva Tirjaková
Acta Protozoologica, Volume 55, Issue 3, 2016, pp. 173 - 188
https://doi.org/10.4467/16890027AP.16.017.5749The response of ciliate communities to cyanobacterial bloom was investigated in a shallow, hypertrophic reservoir in Slovakia, central Europe. Seasonal dynamics of ciliate communities corresponded negatively with course of water bloom formation. The highest numbers and abundances of ciliate species occurred during the spring season when cyanobacterial bloom was not fully developed, while there was an abrupt decrease in both numbers and abundances at the beginning of summer when water bloom culminated. Cyanobacterial blooming thus significantly lowered diversity and equitability of ciliate communities: many rare and sporadic species disappeared and few common taxa flourished and dominated. Nonetheless, these leading ciliates formed a functionally diverse assemblage whose members showed mostly positive contemporaneous and only rarely time-shifted interactions. There were fine filter feeders (Cinetochilum margaritaceum, Dexiotricha granulosa, Paramecium caudatum and Spirostomum teres) grazing heterotrophic bacteria and picocyanobacteria, omnivorous fine to coarse filter feeders (Frontonia leucas) as well as hunters (Coleps hirtus, Holophrya teres and Loxophyllum helus) looking for an individual prey. Also a comparatively rich, anaerobic coenosis comprising various bacterivorous armophoreans and plagiopyleans, developed at the bottom of the reservoir. Our study documents that ciliates form functionally diverse communities with potential to control cyanobacterial blooms in hypertrophic reservoirs.
Eva Tirjaková
Acta Protozoologica, Volume 51, Issue 1, 2012, pp. 39 - 52
https://doi.org/10.4467/16890027AP.12.004.0387The present work describes the morphology and morphometry of a freshwater ciliate, Zosterodasys transversus, using live observation and protargol impregnation. The population from the River Ipeľ, Slovakia is designated as a neotype because (i) no type material is available from the species described by Kahl (1928); (ii) the neotype is consistent with Z. transversus as described by Kahl (1928); (iii) the neotype is from the same biogeographic region as Kahl’s (1928) populations; and (iv) there are several similar species (e.g., Z. agamalievi) whose identity is threatened by the species to be neotypified. The main features of Z. transversus are: (i) a body size of 120–240 × 50–115 μm in vivo; (ii) a broadly to narrowly obovate or elliptical body; (iii) a spherical to very narrowly ellipsoidal macronucleus with a single globular micronucleus nearby; (iv) several scattered contractile vacuoles; (v) an average of 82 ciliary rows, most of which are interrupted by a synhymenium incompletely encircling the body; and (vi) an average of 14 nematodesmal rods strengthening walls of the cyrtos. In the well-growing neotype population, a single cell of a mirror-image type was found. Most of the structures of this monster specimen are similar to those from ordinary cells, except for the double cytostome and cyrtos.