Spatial and temporal changes in phosphorus partitioning within a freshwater cyanobacterial mat community
- 199 Downloads
- 15 Citations
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.
Keywords
Phosphorus partitioning Diurnal changes Sequential fractionation Cyanobacterial mat EPSNotes
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.
References
- Blake RE, O’Neil JR, Surkov AV (2005) Biogeochemical cycling of phosphorus: Insights from oxygen isotope effects of phosphoenzymes. Am J Sci 305:596–620CrossRefGoogle Scholar
- Braissant O, Decho AW, Przekop KM et al (2009) Characteristics and turnover of exopolymeric substances in a hypersaline microbial mat. FEMS Microbiol Ecol 67:293–307CrossRefGoogle Scholar
- 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, HeidelbergGoogle Scholar
- Chandrasekaran R, Lee EJ, Thailambal VG et al (1994) Molecular architecture of a galactoglucan from Rhizobium meliloti. Carbohydr Res 261:279–295CrossRefGoogle Scholar
- Cloete TE, Oosthuizen DJ (2001) The role of extracellular exopolymers in the removal of phosphorus from activated sludge. Water Res 35:3595–3598CrossRefGoogle Scholar
- 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 YorkGoogle Scholar
- Des Marais DJ (1995) The biogeochemistry of hypersaline microbial mats. Adv Microb Ecol 14:251–274Google Scholar
- Dubois M, Gilles KA, Hamilton JK et al (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356CrossRefGoogle Scholar
- Frølund B, Palmgren R, Keiding K et al (1996) Extraction of extracellular polymers from activated sludge using a cation exchange resin. Water Res 30:1749–1758CrossRefGoogle Scholar
- 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 38:507–516CrossRefGoogle Scholar
- Hupfer M, Gächter R, Rüegger H (1995) Poly-P in lake sediments. 31P NMR spectroscopy as a tool for its identification. Limnol Oceanogr 40:610–617CrossRefGoogle Scholar
- Jensen HS, McGlathery KJ, Marino R et al (1998) Forms and availability of sediment phosphorus in carbonate sand of Bermuda seagrass beds. Limnol Oceanogr 43:799–810CrossRefGoogle Scholar
- Jørgensen BB, Revsbech NP, Cohen Y (1983) Photosynthesis and structure of benthic microbial mats: microelectrode and SEM studies of four cyanobacterial communities. Limnol Oceanogr 28:1075–1093CrossRefGoogle Scholar
- 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 32:51–63CrossRefGoogle Scholar
- Kim JG, Rejmánková E (2002) Recent history of sediment deposition in marl- and sand-based marshes of Belize, Central America. Catena 48:267–291CrossRefGoogle Scholar
- Klock JH, Wieland A, Seifert R et al (2007) Extracellular polymeric substances (EPS) from cyanobacterial mats: characterisation and isolation method optimisation. Mar Biol 152:1077–1085CrossRefGoogle Scholar
- 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 84:65–111CrossRefGoogle Scholar
- 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 32:1431–1443CrossRefGoogle Scholar
- Kornberg A (1999) Inorganic polyphosphate: a molecule of many functions. Annu Rev Biochem 68:89–125CrossRefGoogle Scholar
- Moons P, Michiels CW, Aertsen A (2009) Bacterial interactions in biofilms. Crit Rev Microbiol 35:157–168CrossRefGoogle Scholar
- Murphy J, Riley JP (1962) A modified single solution method for determination of phosphate in natural waters. Anal Chim Act 26:31–36CrossRefGoogle Scholar
- 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 48:1993–2008CrossRefGoogle Scholar
- Otsuki A, Wetzel RG (1972) Coprecipitation of phosphate with carbonates in a marl lake. Limnol Oceanogr 17:763–767CrossRefGoogle Scholar
- 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 2:11–26CrossRefGoogle Scholar
- Prescott LM, Harley JP, Klein DA (1996) Microbiology, 3rd edn. McGraw-Hill, New York, pp 51–52Google Scholar
- Rejmánková E, Komárková J (2000) Function of cyanobacterial mats in phosphorus-limited tropical wetlands. Hydrobiol 431:135–153CrossRefGoogle Scholar
- Rejmánková E, Komárková J (2005) Response of cyanobacterial mats to nutrient and salinity changes. Aquat Botan 83(2):87–107CrossRefGoogle Scholar
- 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 81:233–252Google Scholar
- 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 10:189–199CrossRefGoogle Scholar
- 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 702Google Scholar
- Ruttenberg KC (1992) Development of a sequential extraction method for different forms of phosphorus in marine sediments. Limnol Oceanogr 37:1460–1482CrossRefGoogle Scholar
- Sañudo-Wilhelmy SA, Tovar-Sanchez A, Fu FX et al (2004) The impact of surface-adsorbed phosphorus on phytoplankton Redfield stoichiometry. Nature 432:897–901CrossRefGoogle Scholar
- Scinto LJ, Reddy KR (2003) Biotic and abiotic uptake of phosphorus by periphyton in a subtropical freshwater wetland. Aquat Bot 77:203–222CrossRefGoogle Scholar
- 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 50:2057–2062CrossRefGoogle Scholar
- 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: 11–20Google Scholar
- Stal LJ (1995) Physiological ecology of cyanobacteria in microbial mats and other communities. New Phytol 131:1–32CrossRefGoogle Scholar
- Stal LJ, Caumette P (Eds) (1994) microbial mats: structure, development and environmental significance. NATO-ASI Series. Springer, New YorkGoogle Scholar
- Sutherland IW (2001a) The biofilm matrix—an immobilized but dynamic microbial environment. Trends Microbiol 9:222–227CrossRefGoogle Scholar
- Sutherland IW (2001b) Biofilm exopolysaccharides: a strong and sticky framework. Microbiology 147:3–9Google Scholar
- Vadstein O (2000) Heterotrophic, planktonic bacteria and cycling of phosphorus. Phosphorus requirements, competitive ability, and food web interactions. Adv Microb Ecol 16:115–167Google Scholar
- Watanabe K, Imase M, Sasaki K et al (2006) Composition of the sheath produced by the green alga Chlorella sorokiniana. Lett Appl Microbiol 42:538–543CrossRefGoogle Scholar