Abstract
Spatial and temporal changes in phosphorus (P) distribution, partitioning and mobility in the benthic cyanobacterial mat (CBM) were evaluated using sequential chemical fractionation. Total P (TP) content was extremely low, ranging from 0.025 to 0.1 mg g−1 DW. Exchangeable and loosely bound P, which we consider to be mainly associated with extracellular polymeric substances (EPS), constituted the most significant proportion of TP (up to 52%, 55 μg g−1 DW), followed by P associated with the authigenic apatites (up to 35% of TP or 18 μg g−1 DW). While we found virtually no exchange of P with the ambient environment, our results show that the partitioning of P forms within CBM is dependent on spatial and temporal fluctuations of physico-chemical parameters, mainly pH and dissolved oxygen. A conspicuous diurnal increase in the reactive, exchangeable and loosely bound P in the top CBM layers was observed. This observation has important ecological implications, as CBM microorganisms therefore have an increased possibility for P “luxury” uptake during the night. This hypothesis is further supported by the fact that P in the organic fraction rises by as much as 53% in the upper layers during the night, indicating some form of cellular uptake. The P-binding potential of EPS also has ecological or biogeochemical consequences and should be considered in stoichiometrical studies where it represents potential danger for great overestimates of cellular P values or the nutritional status of cells.
Similar content being viewed by others
References
Blake RE, O’Neil JR, Surkov AV (2005) Biogeochemical cycling of phosphorus: Insights from oxygen isotope effects of phosphoenzymes. Am J Sci 305:596–620
Braissant O, Decho AW, Przekop KM et al (2009) Characteristics and turnover of exopolymeric substances in a hypersaline microbial mat. FEMS Microbiol Ecol 67:293–307
Canfield DE, Des Marais DJ (1994) Cycling of carbon, sulphur, oxygen and nutrients in a microbial mat. In: Stal LJ, Caumette P (eds) Microbial mats: structure, development and environmental significance. NATO ASI series G, Ecological Sciences. Springer-Verlag, Berlin, Heidelberg
Chandrasekaran R, Lee EJ, Thailambal VG et al (1994) Molecular architecture of a galactoglucan from Rhizobium meliloti. Carbohydr Res 261:279–295
Cloete TE, Oosthuizen DJ (2001) The role of extracellular exopolymers in the removal of phosphorus from activated sludge. Water Res 35:3595–3598
Decho AW (1999) Function of EPS. In: Wingender J, Neu TR, Flemming HC (eds) Microbial extracellular polymeric substances: characterization, structure, and function. Springer, Berlin, New York
Des Marais DJ (1995) The biogeochemistry of hypersaline microbial mats. Adv Microb Ecol 14:251–274
Dubois M, Gilles KA, Hamilton JK et al (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356
Frølund B, Palmgren R, Keiding K et al (1996) Extraction of extracellular polymers from activated sludge using a cation exchange resin. Water Res 30:1749–1758
Gaiser EE, Scinto LJ, Richards JH et al (2004) Phosphorus in periphyton mats provides the best metric for detecting low-level P enrichment in an oligotrophic wetland. Water Res 38:507–516
Hupfer M, Gächter R, Rüegger H (1995) Poly-P in lake sediments. 31P NMR spectroscopy as a tool for its identification. Limnol Oceanogr 40:610–617
Jensen HS, McGlathery KJ, Marino R et al (1998) Forms and availability of sediment phosphorus in carbonate sand of Bermuda seagrass beds. Limnol Oceanogr 43:799–810
Jørgensen BB, Revsbech NP, Cohen Y (1983) Photosynthesis and structure of benthic microbial mats: microelectrode and SEM studies of four cyanobacterial communities. Limnol Oceanogr 28:1075–1093
Kawaguchi T, Decho AW (2002) Isolation and biochemical characterization of extracellular polymeric secretions (EPS) from modern soft marine stromatolites (Bahamas) and its inhibitory effect on CaCO3 precipitation. Prep Biochem 32:51–63
Kim JG, Rejmánková E (2002) Recent history of sediment deposition in marl- and sand-based marshes of Belize, Central America. Catena 48:267–291
Klock JH, Wieland A, Seifert R et al (2007) Extracellular polymeric substances (EPS) from cyanobacterial mats: characterisation and isolation method optimisation. Mar Biol 152:1077–1085
Komárek J, Komárková-Legnerová J (2007) Taxonomic evaluation of the cyanobacterial microflora from alkaline marshes of northern Belize. 1. Phenotypic diversity of coccoid morphotypes. Nova Hedwig 84:65–111
Kopáček J, Borovec J, Hejzlar J et al (2001) Spectrophotometric determination of iron, aluminum, and phosphorus in soil and sediment extracts after their nitric and perchloric acid digestion. Commun Soil Sci Plant Anal 32:1431–1443
Kornberg A (1999) Inorganic polyphosphate: a molecule of many functions. Annu Rev Biochem 68:89–125
Moons P, Michiels CW, Aertsen A (2009) Bacterial interactions in biofilms. Crit Rev Microbiol 35:157–168
Murphy J, Riley JP (1962) A modified single solution method for determination of phosphate in natural waters. Anal Chim Act 26:31–36
Noe GB, Scinto LJ, Taylor J et al (2003) Phosphorus cycling and partitioning in an oligotrophic Everglades wetland ecosystem: a radioisotope tracing study. Freshwater Biol 48:1993–2008
Otsuki A, Wetzel RG (1972) Coprecipitation of phosphate with carbonates in a marl lake. Limnol Oceanogr 17:763–767
Paerl HW, Pinckney JL, Steppe TF (2000) Cyanobacterial-bacterial mat consortia: examining the functional unit of microbial survival and growth in extreme environments. Environ Microbiol 2:11–26
Prescott LM, Harley JP, Klein DA (1996) Microbiology, 3rd edn. McGraw-Hill, New York, pp 51–52
Rejmánková E, Komárková J (2000) Function of cyanobacterial mats in phosphorus-limited tropical wetlands. Hydrobiol 431:135–153
Rejmánková E, Komárková J (2005) Response of cyanobacterial mats to nutrient and salinity changes. Aquat Botan 83(2):87–107
Rejmánková E, Pope KO, Post R, Maltby E (1996) Herbaceous wetlands of the Yucatan peninsula: communities at extreme ends of environmental gradients. Int Rev Gesamte Hydrobiol 81:233–252
Rejmánková E, Komárek J, Komárková J (2004) Cyanobacteria—a neglected component of biodiversity: patterns of species diversity in inland marshes of northern Belize (Central America). Div Distrib 10:189–199
Richardson C, Vaithiyanathan P, Qualls RG (2008) Water quality, soil chemistry, and ecosystem response to P dosing. In: Richardson C et al (eds) The Everglades experiments—lessons for ecosystem restoration ecological studies, vol 201. Springer, New York, p 702
Ruttenberg KC (1992) Development of a sequential extraction method for different forms of phosphorus in marine sediments. Limnol Oceanogr 37:1460–1482
Sañudo-Wilhelmy SA, Tovar-Sanchez A, Fu FX et al (2004) The impact of surface-adsorbed phosphorus on phytoplankton Redfield stoichiometry. Nature 432:897–901
Scinto LJ, Reddy KR (2003) Biotic and abiotic uptake of phosphorus by periphyton in a subtropical freshwater wetland. Aquat Bot 77:203–222
Sharma K, Inglett PW, Reddy KR et al (2005) Microscopic examination of photoautotrophic and phosphatase-producing organisms in phosphorus-limited Everglades periphyton mats. Limnol Oceanogr 50:2057–2062
Sirová D, Vrba J, Rejmánková E (2006) Extracellular enzyme activities in benthic cyanobacterial mats: comparison between nutrient-enriched and control sites in marshes of northern Belize Source. Aquat Microbiol Ecol 44: 11–20
Stal LJ (1995) Physiological ecology of cyanobacteria in microbial mats and other communities. New Phytol 131:1–32
Stal LJ, Caumette P (Eds) (1994) microbial mats: structure, development and environmental significance. NATO-ASI Series. Springer, New York
Sutherland IW (2001a) The biofilm matrix—an immobilized but dynamic microbial environment. Trends Microbiol 9:222–227
Sutherland IW (2001b) Biofilm exopolysaccharides: a strong and sticky framework. Microbiology 147:3–9
Vadstein O (2000) Heterotrophic, planktonic bacteria and cycling of phosphorus. Phosphorus requirements, competitive ability, and food web interactions. Adv Microb Ecol 16:115–167
Watanabe K, Imase M, Sasaki K et al (2006) Composition of the sheath produced by the green alga Chlorella sorokiniana. Lett Appl Microbiol 42:538–543
Acknowledgment
This research was supported by National Science Foundation grant NSF # 0516159 and partly by Czech grants NAZV QH81012, MSM 6007665801, AV0Z 60050516 and 60170517. We would like to thank Irenio and Russel for help with field sampling.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Borovec, J., Sirová, D., Mošnerová, P. et al. Spatial and temporal changes in phosphorus partitioning within a freshwater cyanobacterial mat community. Biogeochemistry 101, 323–333 (2010). https://doi.org/10.1007/s10533-010-9488-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10533-010-9488-4