https://doi.org/10.4081/jlimnol.2020.1958
Microcosm on a bottle: experimental tests on the colonization of plastic and glass substrates in a retention reservoir
Micro- and macroorganisms in a eutrophic reservoir
Submitted: 30 December 2019
Accepted: 16 March 2020
Published: 27 March 2020
Accepted: 16 March 2020
Abstract Views: 1704
PDF: 464
HTML: 34
HTML: 34
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
The last few decades have seen a dramatic increase in water pollution due to various types of waste generated by human activity. These include plastic and glass accumulating in the shore area of lakes and oceans. These substrates may be colonized by various groups of aquatic organisms. Little is known of the trophic interrelationships between micro- and macroorganisms colonizing plastic (PB) and glass bottles (GB). Therefore, the main objective of the present study was to determine the taxonomic composition and abundance of micro- and macroorganisms colonizing artificial, anthropogenic substrates, the trophic relationships between the organisms colonizing these substrates, and the influence of the physicochemical properties of the water on the formation of such assemblages. Studies of micro- and macroorganisms were carried out on the surface of PB and GB in a eutrophic retention basin. Both the species richness and abundance of microorganisms and metazoa were found to be determined by the type of substrate colonized as well as by the physicochemical properties of the water (primarily the content of total organic carbon and biogenic compounds). Furthermore, the trophic structure of microbial assemblages demonstrated seasonal variability. In spring, the substrates were colonized by typical bacterivorous ciliates, whereas in the following seasons there was a larger share of omnivorous species (ciliates and rotifers). This may indicate that the accumulation of various types of anthropogenic waste, in the present case GB and PB, may contribute to changes in the matter and energy cycle, including the carbon cycle, in various microhabitats of aquatic ecosystems.
Andersen R, Wells C, Macrae M, Price J, 2013. Nutrient mineralization and microbial functional diversity in a restored bog approach natural conditions 10 years post restoration. Soil Biol. Biochem. 64:37-47.
DOI: https://doi.org/10.1016/j.soilbio.2013.04.004
Beaker JH, 1984. Factors affecting the bacterial colonization of various surfaces in a river. Can. J. Microbiol. 30:511-516.
DOI: https://doi.org/10.1139/m84-076
Beaver JR, Crisman TL, 1989. The role of ciliated protozoa in pelagic freshwater ecosystems. Microb. Ecol.17:11-136.
DOI: https://doi.org/10.1007/BF02011847
Bickel SL, Tang KW, Grossart HP, 2012. Ciliate epibionts associated with crustacean zooplankton in German lakes: distribution, motility, and bacterivory. Front. Microbiol. 3:243.
DOI: https://doi.org/10.3389/fmicb.2012.00243
Bołtruszko J., 2011. Epizoic communities of Rotifera on freshwater bivalves. Oceanolog. Hydrobiol. Stud. 39:75-82.
DOI: https://doi.org/10.2478/v10009-010-0053-1
Boothroyd IKG, Dickie BN, 1989. Macroinvertebrates colonisation of perspex artifical substrates for use in biomonitoring studies. New Zealand J. Marine Freshw. Res. 23:467-478.
DOI: https://doi.org/10.1080/00288330.1989.9516383
Boxshall GA, Halsey SH, 2004. An introduction to copepod diversity. Royal Society, Andover, UK.
Carrias JF, Amblard C, Beurdier G, 1998. Seasonal dynamics and vertical distribution of planktonic ciliates and their relationship to microbial food resources in the oligomesotrophic Lake Pavin. Arch. Hydrobiol. 143:227-255.
DOI: https://doi.org/10.1127/archiv-hydrobiol/143/1998/227
Connel JH, 1978. Diversity in tropical rain forest and coral reefs. Science 199:1302-1310.
DOI: https://doi.org/10.1126/science.199.4335.1302
Córaz A, Echevarria F, Gonzalez-Gordillo IJ, Irigoien X, Ubenda B, Hornàndez-León S, 2014. Plastic debris in the open ocean. Proc. Nat. Acad. Sci. 111:10239-10244.
DOI: https://doi.org/10.1073/pnas.1314705111
Dumont HJ, Van de Velde I, Dumont S, 1975. The dry weight estimate of biomass in selection of Cladocera, Copepoda and Rotifera from the plankton, periphyton and benthos of continental waters. Oecologia 19:75-97.
DOI: https://doi.org/10.1007/BF00377592
Ejsmont-Karabin J, Karpowicz M, 2019. Epizoic rotifers on Dreissena polymorpha in relations to biotic factors. Hydrobiologia 828:137-145.
DOI: https://doi.org/10.1007/s10750-018-3808-4
Finlay BJ, 1982. Procedures for the isolation, cultivation and identification of protozoa. Experiment. Microb. Ecol. 1:44-65.
Foissner W, Berger H, Schaumburg J, 1999. Identification and ecology of limnetic plankton ciliates. Informationsberichte des Bayer. Landesamtes für Wasserwirtschaft, München.
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. Freshw. Biol. 35:375-470.
DOI: https://doi.org/10.1111/j.1365-2427.1996.tb01775.x
Gaiser EE, Childers DL, Jones RD, Richards JH, Scinto LJ, Texler JC, 2006. Periphyton responses to eutrophication in the Florida Everglades: cross-system patterns of structural and compositional change. Limnol. Oceanogr. 51:617-630.
DOI: https://doi.org/10.4319/lo.2006.51.1_part_2.0617
Gilbert D, Amblard C, Bourdier G, Francez AJ, 1998. The microbial loop at the surface of a peatland: structure, functioning and impact of nutrients inputs. Microb. Ecol. 35:89-93.
DOI: https://doi.org/10.1007/s002489900062
Golterman HL, 1969. Methods for chemical analysis of freshwaters. Blackwell Scientific Publications, Oxford, Edinburgh.
Gregory MR, 2009. Environmental implications of plastic debris in marine settings-entanglement, ingestion, smothering, hangers-on, hitch-hiking and alien invasions. Phil. Trans.R. Soc. B. 364:2013-2025.
DOI: https://doi.org/10.1098/rstb.2008.0265
Hermanowicz W, Dożańska W, Dolido J, Koziorowski B, 1976. Physical and chemical investigation methods of water and sewage. Arkady, Warsaw, Poland.
Hillebrand H, Sommer U, 2000. Effect of continuous nutrient enrichment on microalgae colonizing hard substrates. Hydrobiologia 426:185-192.
DOI: https://doi.org/10.1007/978-94-011-4148-2_18
Kalinowska K, Ejsmont-Karabin J, Gorelysheva Z, Rybak IJ, 2012. Biomass distribution and dynamics and food web relations in psammon community of a eutrophic lake. Pol. J. Ecol. 60:443–453.
Kaur P, Mehra NK, 1994. An evaluation of a new method for quantitative analysis of epiphytic biota on roots of water hyacinth. Verhandlungen der International Association of Theoretical and Applied Limnology 25:1137-1141.
DOI: https://doi.org/10.1080/03680770.1992.11900620
Law KL, Morèt-Ferguson S, Maximenko NA, Proskurowski G, Peacock EE, Hafner J, Reddy CM, 2010. Plastic accumulation in the North Atlantic subtropical gyre. Sci. 329 (5996):1185-1188.
DOI: https://doi.org/10.1126/science.1192321
Madoni P, Zangrossi S, 2005. Ciliated protozoa and saprobical evaluation of water quality in the Taro River (northern Italy). Ital. J. Zool.72:21-25.
DOI: https://doi.org/10.1080/11250000509356648
Mieczan T, Rudyk-Leuska N, 2019. Seasonal dynamics of the epibiont food web on Unio tumidus (Philipsson, 1788) in eutrophic reservoir. Europ. J. Protistol. 69:138-150.
DOI: https://doi.org/10.1016/j.ejop.2019.04.003
Mieczan T, 2006. Studies on the colonization and succession patterns of periphytic ciliates communities on natural and artificial substrata in two lakes of different trophic status. Pol. J. Environ. Stud. 15/5d:557-561.
Mieczan T, 2007. Comparative study of periphytic ciliate communities colonization and succession on natural and artificial substrata in two shallow lakes (Eastern Poland). Annal. de Limnol. Internat. J. Limnol. 3:179-186.
DOI: https://doi.org/10.1051/limn:2007012
Moeller RE, Burkholder JM, Wetzel RG, 1988. Significance of sedimentary phosphorous to a rooted submersed macrophyte (Najas flexilis (Willd.) Rostk. and Schmidt) and its algal epiphytes. Aquat. Bot. 32:261-281.
DOI: https://doi.org/10.1016/0304-3770(88)90120-9
Napiórkowski P, Bąkowska M, Mrozińska N, Szymańska M, Kolarova N, Obolewski K, 2019. The Effect of Hydrological Connectivity on the Zooplankton Structure in Floodplain Lakes of a Regulated Large River (the Lower Vistula, Poland). Water 11:1924, https://doi.org/10.3390/w11091924.
DOI: https://doi.org/10.3390/w11091924
Oberbeckmann S, Osborn AM, Duhaime MB, 2016. Microbes on a bottle: substrate, season and geography influence community composition on microbes colonizing marine plastic debris. PLOS One, doi: 10.1371/journal.pone.0159289.
DOI: https://doi.org/10.1371/journal.pone.0159289
Pernthaler J., Glöckner F.O., Schonhuber W., Amann R. 2001. Fluorescence in situ hybridization with rRNA-targeted aligonucleotide probes. Methods Microbiol. 30:207-226.
DOI: https://doi.org/10.1016/S0580-9517(01)30046-6
Porter KG, Feig YS, 1980. The use of DAPI for identifying and counting aquatic microflora. Limnol. Oceanogr. 25:943-948.
DOI: https://doi.org/10.4319/lo.1980.25.5.0943
Primc-Habdija B, Habdija J, Plenković-Moraj A, Špoljar M, 1997. The overgrowth capacity of periphyton on artificial substrates exposed at vertical profile in the Lake Visovac. Period. Biol. 99:403-408.
Rott E, 1981. Some results from phytoplankton counting intercalibrations. Schweiz. Z. Hydrol. 43:34-62.
DOI: https://doi.org/10.1007/BF02502471
Ruttner-Kolisko A, 1974. Plankton rotifers: biology and taxonomy. Die Binnengewässer, Stuttgart, Germany.
Strüder-Kypke MC, 1999. Periphyton and sphagnicolus protists of dystrophic bog lakes (Brandenburg, Germany). Limnologica 29:393-406.
DOI: https://doi.org/10.1016/S0075-9511(99)80047-4
Ter Braak CJF, Šmilauer P, 2002. CANOCO–FORTRAN program for Canonical Community Ordination (vers. 2.1). Microcomputer Power, Ithaca.
van den Hoek C, Mann DG, Jahns HM, 1995. Algae. An introduction to phycology. Cambridge University Press, Cambridge.
Wang T, Li Y, Xu T, Wu N, Liang M, Hynds P, 2016. Biofilm microbial community structure in an urban lake utilizing reclaimed water. Environ. Earth. Sci. 75:314.
DOI: https://doi.org/10.1007/s12665-015-5197-6
Edited by
Andrea Di Cesare, CNR-IRSA Verbania, ItalyHow to Cite
Mieczan, Tomasz. 2020. “Microcosm on a Bottle: Experimental Tests on the Colonization of Plastic and Glass Substrates in a Retention Reservoir: Micro- and Macroorganisms in a Eutrophic Reservoir”. Journal of Limnology 79 (3). https://doi.org/10.4081/jlimnol.2020.1958.
Similar Articles
- Ana Sanz, Manuel J. López-Rodríguez, Sergio García-Mesa, Cristina Trenzado, Rosa M. Ferrer, J. Manuel Tierno de Figueroa, Are antioxidant capacity and oxidative damage related to biological and autecological characteristics in aquatic insects? , Journal of Limnology: Vol. 76 No. 1 (2017)
- Juri NASCIMBENE, Daniel SPITALE, Holger THÜS, Marco CANTONATI, Congruencies between photoautotrophic groups in springs of the Italian Alps: implications for conservation strategies , Journal of Limnology: Vol. 70 No. s1 (2011): Springs: neglected key habitats for biodiversity conservation
- Martin Schmid, KellyAnn Ross, Alfred Wüest, Comment on An additional challenge of Lake Kivu in Central Africa – upward movement of the chemoclines by Finn Hirslund , Journal of Limnology: Vol. 71 No. 2 (2012)
- . Issa, Festus Aka Tongwa, Alfred G. Mouliom, Dmitri Rouwet, Wilson Y. Fantong, Boris Chako Tchamabé, Takeshi Ohba, Yutaka Yoshida, Daniel Sighomnou, Nkamdjou Sigha, Minoru Kusakabe, δ18O and δD variations in some volcanic lakes on the Cameroon Volcanic Line (West-Africa): generating isotopic baseline data for volcano monitoring and surveillance in Cameroon , Journal of Limnology: Vol. 74 No. 1 (2015)
- Elena LEGNANI, Diego COPETTI, Alessandro OGGIONI, Gianni TARTARI, Maria Teresa PALUMBO, Giuseppe MORABITO, Planktothrix rubescens’ seasonal dynamics and vertical distribution in Lake Pusiano (North Italy) , Journal of Limnology: Vol. 64 No. 1 (2005)
- Markus A. Hoffmann, Alberto Benavent González, Uta Raeder, Arnulf Melzer, Experimental weed control of Najas marina ssp. intermedia and Elodea nuttallii in lakes using biodegradable jute matting , Journal of Limnology: Vol. 72 No. 3 (2013)
- Franco Tassi, Dmitri Rouwet, An overview of the structure, hazards, and methods of investigation of Nyos-type lakes from the geochemical perspective , Journal of Limnology: Vol. 73 No. 1 (2014)
- Ulrike OBERTEGGER, Marina MANCA, Response of rotifer functional groups to changing trophic state and crustacean community , Journal of Limnology: Vol. 70 No. 2 (2011)
- Gregor Muri, Atmospheric deposition chemistry in a subalpine area of the Julian Alps, North-West Slovenia , Journal of Limnology: Vol. 72 No. 2 (2013)
- Alireza Keikhosravi, Sara Fratini, Christoph D. Schubart, Population genetic structure and demographic history of the freshwater crab Potamon elbursi (Brachyura: Potamidae) from the Alborz Mountains in northern Iran , Journal of Limnology: Vol. 74 No. 3 (2015)
<< < 46 47 48 49 50 51 52 53 54 55 > >>
You may also start an advanced similarity search for this article.
List of Cited By :
