Communities structure and relation to water pH of testate amoebae (Amoebozoa, Rhizaria) in reservoirs in Northeastern Bulgaria

Authors

  • Rositsa Davidova Faculty of natural sciences, Konstantin Preslavsky University of Shumen, Shumen
  • Dimitar Doychev Department of biology, Faculty of natural sciences, Konstantin Preslavsky University of Shumen, 115 Universitetska street, Shumen, Bulgaria

DOI:

https://doi.org/10.5281/zenodo.15512891

Keywords:

bioindicators, diversity, dominance, ecosystems

Abstract

The identification of variability in testate amoebae communities and their environmental dependencies makes it possible to clarify many issues related to the changes in natural and artificial ecosystems. The present study covers the benthic testate amoebae fauna of seven reservoirs - Brestovene, Beli Lom, Loznitsa, Kara Michal, Bogdantsi, Isperih and Lipnik. Regression analysis and canonical correspondence analysis were performed to determine differences in testate amoebae communities between reservoirs. The obtained results show that in Bogdantsi reservoir only two genera - Centropyxis and Difflugia, dominate, which, together with the established extremely low taxonomic diversity and abundance of testate amoebae, is an indication of the presence of strong eutrophication and unsuitable conditions in it. In the Loznitsa and Beli Lom reservoirs dominance is distributed among a large number of genera, a significantly larger number of species and individuals are found, which indicates the presence of a sustainable and suitable environment for development of testate amoebae. Our CCA results suggest that species distribution differs along the pH gradient. The species Centropyxis aerophila, C. aerophila v. sphagnicola, Difflugia pristis and Schonbornia viscicula have a very positive correlation with pH, while Cyclopyxis ambigua, Difflugia minuta and D. elegans have a negative correlation with pH.

References

Arrieira, R.L., Alves, G.M., Schwind, L.T.F., & Lansac-Tôha, F.A. (2015). Local factors affecting the testate amoeba community (protozoa: Arcellinida; Euglyphida) in a neotropical floodplain. Journal of Limnology, 73(3), 444–452.

Arrieira, R.L., Schwind, L.T.F., Joko, C.Y., Alves, G.M., Velho, L.F.M., & Lansac-Tôha, F.A. (2016). Relationships between environmental conditions and the morphological variability of planktonic testate amoeba in four neotropical floodplains. European Journal of Protistology, 56, 180–190.

Arrieira, R.L., Schwind, L.T.F., Bonecker, C.C., & Lansac-Tôha, F.A. (2017). Environmental factors exert predominant effects on testate amoeba metacommunities during droughts in foodplains. Austral. Ecol., 42, 210–217. https://doi.org/10.1111/aec.12423

Asioli, A., Medioli, F.S., & Patterson, R.T. (1996). Thecamoebians as a tool for reconstruction of paleoenvironments in some Italian lakes in the foothills of the Southern Alps (Orta, Varese and Canada). J. Foraminiferal Res., 26, 248–263.

Barnett, R., Garneau, M., & Bernatchez, P. (2016). Salt-marsh sea-level indicators and transfer function development for the Magdalen Islands in the Gulf of St. Lawrence, Canada. Marine Micropaleontology, 122, 13–26.

Beyens, L., & Meisterfeld, R. (2001). Protozoa: testate amoebae. In J.P. Smol, H.J.B. Birks, & W.M. Last (Eds.), Tracking Environmental Changes Using Lake Sediments (pp. 121–153). Kluwer Academic Publishers, Dordrecht.

Bobrov, A.A., Charman, D.J., & Warner, B.G. (1999). Ecology of testate amoebae (Protozoa: Rhizopoda) on peatlands in western Russia with special attention to niche separation in closely related taxa. Protistology, 150, 125–136.

Booth, R.K. (2002). Testate amoebae as paleoindicators of surfacemoisture changes on Michigan peatlands: modern ecology and hydrological calibration. J Paleolimnology, 28, 329–348.

Dalby, A.P., Kumar, A., Moore, J.M., & Patterson, R.T. (2000). Utility of arcellaceans (thecamoebians) as paleolimnological indicators in tropical settings: Lake Sentani, Irian Jaya, Indonesia. J. Foraminiferal Res., 30, 135–142.

Escobar, J., Brenner, M., Whitmore, T.J., Kenney, W.F., & Curtis, J.H. (2008). Ecology of testate amoebae (thecamoebians) in subtropical Florida lakes. J. Paleolimnology, 40, 715–731. https://doi.org/10.1007/s10933-008-9195-5.

Freitas, Y., Ramos, B., da Silva, Y., Sampaio, G., Nascimento, L., Branco, C., & Miranda, V. (2022). Testate amoebae: a review on their multiple uses as bioindicators. Acta Protozoologica, 61, 1–9.

Jassey, V.E.J., Chiapusio, G., Gilbert, D., Toussaint, M.-L., & Binet, P. (2012). Phenoloxidase and peroxidase activities in Sphagnum dominated peatland in a warming climate. Soil Biol. Biochem. 46, 49–52.

Heger, T. J., Derungs, N., Theurillat, J.P., & Mitchell, E. A. D. (2016). Testate Amoebae Like It Hot: Species Richness Decreases Along a Subalpine-Alpine Altitudinal Gradient in Both Natural Calluna vulgaris Litter and Transplanted Minuartia sedoides Cushions. Microb. Ecol., 71, 725–734.

Kumar, A., & Patterson, R.T. (2000). Arcellaceans (Thecamoebians): New Tools for Monitoring Long-and Short-Term Changes in Lake Bottom Acidity. Environ. Geol., 39, 689–697.

Kur’ina, I. V., Preis, Yu. I., & Bobrov, A. A. (2010). Testate Amoebae Inhabiting Middle Taiga Bogs in Western Siberia. Biology Bulletin, 37, 4, 357–362.

Lorencova, M. (2009). Thecamoebians from recent lake sediments from the Sumava Mts, Czech Republic. Bulletin of Geosciences, 84(2), 359–376.

Macumber, A.L., Patterson, R.T., Roe, H.M., Reinhardt, E.G., Neville, L.A., & Swindles, G.T. (2014). Autoecological approaches to resolve subjective taxonomic divisions within the Arcellacea. Protist, 165, 3, 305–316.

Mieczan, T. (2007a). Epiphytic protozoa (Testate amoebae, Ciliates) associated with Sphagnum in peatbogs: relationship to chemical parameters. Polish Journal of Ecology, 55, 79–90.

Mieczan, T. (2007b). Seasonal patterns of testate amoebae and ciliates in three peatbogs: relationship to bacteria and flagellates (Poleski National Park, Eastern Poland). Ecohydrol Hydrobiol., 1, 295–305.

Mieczan, T., & Adamczuk, M. (2015). Ecology of testate amoebae (Protists) in mosses: distribution and relation of species assemblages with environmental parameters (King George Island, Antarctica). Polar Biology, 38, 221–230.

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 Phytology, 145, 95–106.

Mitchell, E.A.D., & Gilbert, D. (2004). Vertical micro-distribution and response to nitrogen deposition of testate amoebae in Sphagnum. J. Eukaryot. Microbiology, 51, 480–490.

Nasser, N.A., Patterson, R.T., Roe, H.M., Galloway, J.M., Falck, H., Palmer, M.J., Spence, C., Sanei, H., Macumber, A.L., & Neville, L.A. (2016). Lacustrine Arcellinina (testate amoebae) as bioindicators of arsenic contamination. Microb. Ecology, 72, 130–149.

Ndayishimiye, J.C., Lin, T., Nyirabuhoro, P., Zhang, G., Zhang, W., Mazei, Y., Ganjidous, H., & Yang, J. (2021). Decade-scale change in testate amoebae community primarily driven by anthropogenic disturbance than natural change in a large subtropical reservoir. Sci Total Environ., 784, 147026. https://doi.org/10.1016/j.scitotenv. 2021.147026

Nguyen-Viet, H., Bernard, N., Mitchell, E.A.D., Badot, P.-M., & Gilbert, D. (2008). Effect of lead pollution on testate amœbæ communities living in Sphagnum fallax: an experimental study. Ecotoxicol. Environ. Saf., 69, 130–138.

Opravilova, V., & Hajek, M. (2006). The variation of testacean assemblages (Rhizopoda) along the complete base-richness gradient in fens: a case study from the Western Carpathians. Acta Protozoologica, 45, 191–204.

Patterson, R.T., MacKinnon, K.D., Scott, D.B., & Medioli, F.S. (1985). Arcellaceans (Thecamoebians) in small lakes of New Brunswick and Nova Scotia: modern distribution and Holocene stratigraphic changes. J. Foraminiferal Res., 15 (2), 114–137. https://doi.org/10.2113/gsjfr.15.2.114.

Patterson, R.T., Burbidge, S.M., & Baker, T. (1996). Arcellaceans (thecamoebians) as proxies of arsenic and mercury contamination in northeastern Ontario lakes. J. Foraminiferal Res., 26, 172–183.

Patterson, R.T., & Kumar, A. (2000). Assessment of arcellacean (thecamoebian) assemblages, species, and strains as contaminant indicators in James Lake, Northeastern Ontario, Canada. J. Foraminiferal Res., 30, 310–320.

Patterson, R.T., Dalby, A., Kumar, A., Henderson, L.A., & Boudreau, R.E. (2002). Arcellaceans (thecamoebians) as indicators of land-use change: settlement history of the Swan Lake area, Ontario as a case study. J. Paleolimnol., 28 (3), 297–316.

Patterson, R., Roe, H., & Swindles, G. (2012). Development of an Arcellacea (testate lobose amoebae) based transfer function for sedimentary phosphorus in lakes. Palaeogeogr. Palaeocl., 348-349, 32–44.

Patterson, R., Lamoureux, E., Neville, L., & Macumber, A. (2013). Arcellacea (Testate Lobose Amoebae) as PH Indicators in a Pyrite Mine-Acidified Lake, Northeastern Ontario, Canada. Microb. Ecol., 65, 541–554.

Payne, R. (2010). Testate amoeba response to acid deposition in a Scottish Peatland. Aquat. Ecol., 44, 373–385.

Proctor, M., & Maltby, E. (1998). Relations between acid atmospheric deposition and the surface pH of some ombrotrophic bogs in Britain. J Ecol., 86, 329–340.

Qin, Y., Booth, R.K., Gu, Y., Wang, Y., & Xie, S. (2009). Testate amoebae as indicators of 20th century eutrophication in Lake Zhangdu, China. Fund. Appl. Limnol., 175 (1), 29–38. https://doi.org/10.1127/1863-9135/2009/0175-0029.

Qin, Y., Fournier, B., Lara, E., Gu, Y., Wang, H., Cui, Y., Zhang, X., & Mitchell, E. (2013). Relationships between Testate Amoeba Communities and Water Quality in Lake Donghu, a Large Alkaline Lake in Wuhan, China. Front. Earth Sci., 7, 182–190.

Qin, Y., Bobrov, A., Puppe, D., Li, H., Man, B., Gong, J., Wang, J., Cui, Y., Gu, Y., Herzschuh, U., & Xie, S. (2024). Testate amoebae (Protozoa) in lakes of the Qinghai-Tibet plateau: biodiversity, community structures, and protozoic biosilicification in relation to environmental properties and climate warming. Science of The Total Environment, 913, 169661, 1-14. https://doi.org/10.1016/j.scitotenv.2023.169661

Roe, H.M., & Patterson, R.T. (2006). Distribution of thecamoebians (testate amoebae) in small lakes and ponds, Barbados, West Indies. J. Foraminiferal Res., 36 (2), 116–134.

Roe, H., Patterson, R., & Swindles, G. (2010). Controls on the contemporary distribution of lake thecamoebians (testate amoebae) within the Greater Toronto Area and their potential as water quality indicators. J. Paleolimnol., 43, 955-975.

Roe, H., & Patterson, R. (2014). Arcellacea (testate amoebae) as bio-indicators of road salt contamination in lakes. Microb. Ecol., 68 (2), 299–313.

Siver, P.A., Lott, A.M., & Torres, P. (2020). Abundance and distribution of testate amoebae bearing siliceous plates in freshwater lakes and ponds along the east coast of North America: importance of water depth and pH. Freshw Sci., 39, 791–803. https://doi.org/10.1086/711691

Song, L., Li, H., Wang, K., Yan, X., & Wu, D. (2018). Seasonal dynamics in the community structure and trophic structure of testate amoebae inhabiting the Sanjiang peatlands, Northeast China. European Journal of Protistology, 63, 51–61.

Sysoev, V., Seleznev, D., Tran, H., Reshetnikov, F., & Tikhonenkov, D. (2024). Can the morphological traits of benthic testate amoebae in a freshwater lake be indicators of depth and environmental conditions? Limnology. https://doi.org/10.1007/s10201-024-00758-5

Swindles, G.T., & Roe, H.M. (2007). Examining the dissolution characteristics of testate amoebae (Protozoa: Rhizopoda) in low pH conditions: implications for peatland palaeoclimate studies. Palaeogeogr., 252, 486–496.

Tran, H.Q., Tran, V.T.H., & Tikhonenkov, D.V. (2021). Freshwater testate amoebae from waterbodies of north Vietnam with the fnding of indicator species. Limnology, 22, 151–160.

Tsyganov, A.N., Aerts, R., Nijs, I., Cornelissen, J.H.C., & Beyens, L. (2012). Sphagnum-dwelling testate amoebae in subarctic bogs and more sensitive to soil warming in the growing season than in winter: the results of 8-year field climate manipulations. Protist, 163, 400–414.

Tsyganov, A., Malysheva, E., Zharov, A., Sapelko, T., & Mazei, Y. (2019). Distribution of benthic testate amoeba assemblages along a water depth gradient in freshwater lakes of the Meshchera Lowlands, Russia, and utility of the microfossils for inferring past lake water level. J Paleolimnology, 62, 137–150. https://doi.org/10.1007/s10933-019-00080-6

Vincke, S., Ledeganck, P., Beyens, L., & Van De Vijver, B. (2004). Soil testate amoebae from sub-Antarctic Iles Crozet. Antarctic Science, 16 (2), 165–174.

Wall, A., Magny, M., Mitchell, E., Vannière, B., & Gilbert, D. (2010). Response of testate amoeba assemblages to environmental and climatic changes during the Lateglacial-Holocene transition at Lake Lautrey (Jura Mountains, eastern France). Journal of Quaternary Science, 25(6), 945–956.

Downloads

Published

2025-05-26

How to Cite

Davidova, R., & Doychev, D. (2025). Communities structure and relation to water pH of testate amoebae (Amoebozoa, Rhizaria) in reservoirs in Northeastern Bulgaria. Journal of Wildlife and Biodiversity, 9(2), 258–273. https://doi.org/10.5281/zenodo.15512891