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Testate amoebae and ciliates are common inhabitants of moist soils, lakes and peatbogs. These microorganisms are important consumers of bacteria, flagellates and algae; they also participate in transformation of the organic matter and nutrient regeneration. The complexity of micro-environmental conditions present in peatbogs and the challenges associated with the proper sampling may partly explain the fact that these microorganisms are still much less studied than other components of the ecosystem. The influence of emergent and submerged plants on community composition, abundance and biomass of testate amoebae and ciliates were investigated in two peatbogs in the eastern Poland. The raised and carbonate bogs selected for this study were considered to be representative of the bogs of the region and contained a broad diversity of habitats. Samples were collected in patches of Sphagnum angustifolium (C.C.O. Jensen ex Russow), Sphagnum cuspidatum Ehrh. ex Hoffm., Sphagnum palustre L., belts of Phragmites australis (Car.), Typha latifolia L., Carex acutiformis Ehrhart., Calliergonella cuspidata (Hedw.) and beds of Utricularia sp. Sampling was done on a monthly basis from April to November. At each plant patch (microhabitat) and each sampling date the water was sampled using a plexiglass core (length 1.0 m, [Radius]50 mm). Comparison of the species number, abundance and biomass (estimated in C organic units) of testate amoebae and ciliates between Sphagnum patches did not show statistically significant differences. The significant differences were noted in patches of plants in carbonate peatbog. The highest species number (40-46) was found in the Utricularia and Calliergonella, and the lowest richness (26-20) in the Typha, Phragmites and Carex. The density and biomass of protozoa communities, increase together with the abundance and the level of the complicated spatial structure of the plants. Based on differences in plant structure, two groups of habitats with similar patterns of size-related testate amoebae and ciliate distribution were distinguished. The first group consisted of three vegetated zones of smooth stem structure (Phragmites, Typha and Carex), the second group comprised plant species, which were more complex (Sphagnum, Utricularia and Calliergonella). In the redundancy analysis, water level, pH, concentration of TP, chlorophyll a and TOC together explain 45% of the variation in the species distribution data. The contribution of conductivity, dissolved oxygen TN and DOC was not (or marginally) statistically significant.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
135--144
Opis fizyczny
Bibliogr. 30 poz.,Rys., tab.,
Twórcy
autor
- Department of Hydrobiology and Ichthyobiology, Laboratory of Nature Protection and Landscape Ecology, University of Agriculture, Dobrzańskiego 37, 20-262 Lublin, Poland
Bibliografia
- 1. Clarke K.J. 2003 – Guide to the identification of soil protozoa – Testate Amoebae – Freshwater Biological Association, UK, 40 pp.
- 2. Charman D.J., Hendon D., Woodland W. 2000 – The identification of testate amoebae (Protozoa: Rhizopoda) in peats – Quatenary Research. Technical Guide, 147 pp.
- 3. Foissner W., Berger H., Kohmann F. 1994 – Taxonomische und ökologische Revision der Ciliaten des Saprobiensystems. Hymenostomatida, Prostomatida, Nassulida. Informationsberichte des Bayer – Landesamtes für Wasserwirtschaft, München, 548 pp.
- 4. Foissner W., Berger H. 1996 – A user-friendly guide to the ciliates (Protozoa, Ciliophora) commonly used by hydrobiologists as bioindicators in rivers, lakes and waste waters, with notes on their ecology – Freshwater Biol. 35: 375–470.
- 5. Foissner W., Berger H., Schaumburg J. 1999 – Identification and Ecology of Limnetic Plankton Ciliates. Informationsberichte des Bayer – Landesamtes für Wasserwirtschaft, München, 777 pp.
- 6. Gilbert D., Amblard C., Bourdier G., Francez A.J. 1998 – The microbial loop at the surface of a peatland: structure, functioning and impact of nutrients inputs – Microb. Ecol. 35: 89–93.
- 7. Gilbert D., Mitchell E.A.D. 2006 – Microbial diversity in Sphagnum peatlands (In: Peatlands: Evolution and records of environmental and climate changes, Eds: I.P. Martini, A. Martinez Cortizas, Chesworth) – Elsevier, pp. 287–318.
- 8. Golterman H.L. 1969 – Methods for chemical analysis of freshwaters – Blackwell Scientific Publications, Oxford, Edinburgh, 213 pp.
- 9. Grolière C.A. 1977 – Contribution à l’ètude de quelques ciliès des sphaignes: II – Dynamique des populations – Protistologica, 13: 335–352.
- 10. Hann B.J. 1995 – Invertebrate associations with submersed aquatic plants in a prairie wetland – UFS (Delta Marsh) Annual Report, 30:78–84.
- 11. Jauhiainen S. 2002 – Testacean amoebae in different types of mire following drainage and subsequent restoration – Eur. J. Protistol. 38: 59–72.
- 12. Kooijman A.M., Paulissen M.P.C.P. 2006 – Higher acidification rates in fens with phosphorus enrichment – Applied Vegetation Science, 9: 205–212.
- 13. Kuczyńska-Kippen N. 2005 – On body size and habitat selection in rotifers in a macrophyte-dominated lake Budzyńskie, Poland – Aquatic Ecol. 39: 477–454.
- 14. Lamentowicz M., Mitchell E.A. 2005 – The ecology of Testate amoebae (Protists) in Sphagnum in north-western Poland in relation to peatland ecology – Microb. Ecol. 50: 48–63.
- 15. Lamentowicz Ł, Gąbka M., Lamentowicz M. 2007 – Species composition of testate amoebae (Protists) and environmental parameters in Sphagnum peatland – Pol. J. Ecol. 55: 749–759.
- 16. Mazei Yu. A., Tsyganov A.N., Bubnova O.A. 2007 – Structure of community of testate amoebae in a sphagnum dominated bog in upper sura flow (Middle Volga Territory) – Ecology, 4: 462–474.
- 17. Mieczan T. 2007 – Epiphytic protozoa (Testate amoebae, Ciliates) associated with Sphagnum in peatbogs: relationship to chemical parameters – Pol. J. Ecol. 55: 79–90.
- 18. Mieczan T. 2008 – Impact of emergent and submerged macrophytes on planktonic ciliates in shallow freshwater lakes (Eastern Poland) – Internat. Rev. Hydrobiol. 93: 269–283.
- 19. Mieczan T. 2009a – Ciliates in Sphagnum peatlands: vertical micro-distribution, and relationships of species assemblages with environmental parameters – Zoological Studies, 48: 33–48.
- 20. Mieczan T. 2009b – Ecology of testate amoebae (Protists) in Sphagnum peatlands of eastern Poland: vertical micro-distribution and species assemblages in relation to environmental parameters – Ann. Limnol.-Int. J. Limnol. 45: 41–49.
- 21. Mitchell E.A.D., Buttler A., Grosvernier Ph., Hydin H., Albinsson C., Greenup A.L., Heijmans M.M.P.D., Hoosbeek M.R., Saarinen T. 2000 – Relationships among testate amoebae (Protozoa), vegetation and water chemistry in five Sphagnum-dominated peatlands in Europe – New Phytol. 145: 95–106
- 22. Mitchell E.A.D., Bragazza L., Gerdol R. 2004 – Testate amoebae (Protista) communities in Hylocomium splenders (Hedw.) B.S.G. (Bryophyta): relationships with altitude, and moss elemental chemistry – Protist, 155: 423–436.
- 23. Mitchell E.A.D., Gilbert D. 2004 – Vertical micro-distribution and response to nitrogen deposition in testate amoebae in Sphagnum – J. Eukaryot. Microbiol. 51: 480–490.
- 24. MVSP. 2002 – Multivariate Statistical Package – Kovach Computering Services.
- 25. Payne R.J., Mitchell E.A.D. 2007 – Ecology of testate amoebae from mires in the Central Rhodope Mountains, Greece and development of transfer function for paleohydrological reconstruction – Protist, 158: 159–171.
- 26. Sirová D., Borovec J., Černá B., Rejmánková E., Adamec L. 2009 – Microbial community development in the traps of aquatic Utricularia species – Aquatic Botany, 90: 129–136.
- 27. Ter Braak C.J.F. (1988–1992) CANOCO–FORTRAN program for Canonical Community Ordination (vers. 2.1) – Microcomputer Power, Ithaca.
- 28. Tolonen K., Warner B.G., Vasander H. 1994 – Ecology of Testaceans (Protozoa, Rhizopoda) in mires in Southern Finland. 2. Multivariate-Analysis – Arch. Protistenkunde, 144: 97–112.
- 29. Walsh E.J. 1995 – Habitat-specific predation susceptibilities of a littoral rotifer to two invertebrate predators – Hydrobiologia, 313/314: 205–211.
- 30. Warfe D.M., Barmuta L.A. 2006 – Habitat structural complexity mediates food web dynamics in a freshwater macrophyte community – Oecologia, 150: 141–154.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BGPK-2912-1457