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Highly efficient silica sink in monomictic Lake Biwa in Japan

Published online by Cambridge University Press:  18 June 2013

Naoshige Goto*
Affiliation:
School of Environmental Science, The University of Shiga Prefecture, 2500 Hassaka-cho, Hikone, Shiga 522-8533, Japan
Hisayuki Azumi
Affiliation:
School of Environmental Science, The University of Shiga Prefecture, 2500 Hassaka-cho, Hikone, Shiga 522-8533, Japan
Tetsuji Akatsuka
Affiliation:
School of Environmental Science, The University of Shiga Prefecture, 2500 Hassaka-cho, Hikone, Shiga 522-8533, Japan
Masaki Kihira
Affiliation:
Iga Community-Based Research Institute, Mie University, 1-3-3 Yumegaoka, Iga, Mie 518-0131, Japan
Masakazu Ishikawa
Affiliation:
School of Environmental Science, The University of Shiga Prefecture, 2500 Hassaka-cho, Hikone, Shiga 522-8533, Japan
Kaori Anbutsu
Affiliation:
Fisheries and Environmental Oceanography, Graduate School of Agriculture, Kyoto University, Kitashirakawa, Sakyo-ku, Kyoto 606-8502, Japan
Osamu Mitamura
Affiliation:
School of Environmental Science, The University of Shiga Prefecture, 2500 Hassaka-cho, Hikone, Shiga 522-8533, Japan
*
*Corresponding author: [email protected]
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Abstract

In order to clarify the mechanisms underlying high efficiency of the silica sink in monomictic Lake Biwa in Japan, vertical flux of biogenic silica (BSi) was measured using sediment traps over a period of 15 months. The sediment traps were deployed at depths of 30 and 70 m. On a global scale, BSi fluxes in Lake Biwa were very high, ranging from 20 to 1087 mg Si.m−2.d−1 at the 30 m trap and 12–999 mg Si.m−2.d−1 at the 70 m trap throughout the observation period. The BSi fluxes at both traps increased significantly during the winter period and the ratio of BSi fluxes in the winter period to annual BSi fluxes ranged from 27 to 62%. In the winter period, when nutrients are supplied from the hypolimnion to the epilimnion, the distribution of photosynthetically active diatoms was almost homogeneous in all layers, including the aphotic layer. At this time, the diatoms assimilated dissolved silica (DSi) in a wider layer containing a part of aphotic layer in order to produce rigid frustules, which accumulated rapidly in bottom sediments as DSi concentration in the water column decreased. Thus, size of the silica sink in Lake Biwa is enhanced during the winter holomictic mixing period through interaction between physical (thermocline disruption: transfer of diatoms to deep layers by vertical convection), chemical (nutrient supply from deep layers) and biological (dominance of active diatoms in all layers) processes.

Type
Research Article
Copyright
© EDP Sciences, 2013

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References

Azumi, H., Goto, N. and Mitamura, O., 2009. Regeneration of silicic acid from sediment in Lake Biwa, Japan. Verh. Int. Verein. Limnol., 30, 10411045.Google Scholar
Bendschneider, K. and Robinson, R.J., 1952. A new spectrophotometric method for the determination of nitrite in sea water. J. Mar. Res., 11, 8796.Google Scholar
Billen, G., Lancelot, C. and Meybeck, M., 1991. N, P, and Si retention along the aquatic continuum from land to ocean. In: Matoura, R.F.C., Martin, J.M. and Wollast, R. (eds.), Ocean Margin Processes in Global Change, Wiley and Sons, Chichester, 1944.Google Scholar
Bootsma, H.A., Hecky, R.E., Johnson, T.C., Kling, H.J. and Mwita, J., 2003. Inputs, outputs, and internal cycling of silica in a large, tropical lake. J. Great. Lakes. Res., 29, 121138.CrossRefGoogle Scholar
Conley, D.J., 2002. Terrestrial ecosystems and the global biogeochemical silica cycle. Global Biogeochem. Cy., 16, 68-168-8.CrossRefGoogle Scholar
Conley, D.J., Schelske, C.L. and Stoermer, E.F., 1993. Modification of the biogeochemical cycle of silica with eutrophication. Mar. Ecol. Progr. Ser., 101, 179192.CrossRefGoogle Scholar
DeMaster, D.J., 1981. The supply and accumulation of silica in the marine environment. Geochim. Cosmochim. Acta, 45, 17151732.CrossRefGoogle Scholar
Fujinaga, T. and Hori, T., 1982. Analytical methods of lake water. In: Environmental Chemistry on Lake Biwa, Japan Society for the Promotion and Science, Tokyo, 113131 (in Japanese).Google Scholar
Garnier, J., Beusen, A., Thieu, V., Billen, G. and Bouwman, L., 2010. N:P:Si nutrient export ratios and ecological consequences in coastal seas evaluated by the ICEP approach. Global Biogeochem. Cy., 24, BG0A05.CrossRefGoogle Scholar
Gong, G.C., Chang, J., Chiang, K.P., Hsiung, T.M., Hung, C.C., Duan, S.W. and Codispoti, L.A., 2006. Reduction of primary production and changing of nutrient ratio in the East China Sea: effect of the three Gorges dam? Geophys. Res. Lett., 33, L07610.CrossRefGoogle Scholar
Goto, N., Iwata, T., Akatsuka, T., Ishikawa, M., Kihira, M., Azumi, H., Anbutsu, K. and Mitamura, O., 2007. Environmental factors which influence the sink of silica in the limnetic system of the large monomictic Lake Biwa and its watershed in Japan. Biogeochemistry, 84, 285295.CrossRefGoogle Scholar
Goto, N., Kihira, M. and Ishida, N., 2008. Seasonal distribution of photosynthetically active phytoplankton using pulse amplitude modulated (PAM) fluorometry in the large monomictic Lake Biwa, Japan. J. Plankton. Res., 30, 11691177.CrossRefGoogle Scholar
Hofmann, A., Roussy, D. and Filella, M., 2002. Dissolved silica budget in the North basin of Lake Lugano. Chem. Geol., 182, 3555.CrossRefGoogle Scholar
Holm-Hansen, O., Lorenzen, C.J., Holmes, R.W. and Strickland, J.D.H., 1965. Fluorometric determination of chlorophyll. J. Cons. Cons. Int. Explor. Mer., 30, 315.CrossRefGoogle Scholar
Homborg, C., Pastuszak, M., Aigars, J., Siegmund, H., Mörth, C.-M. and Ittekkot, V., 2006. Decreased silica land-sea fluxes through damming in the Baltic Sea catchment – Significance of particle trapping and hydrological alterations. Biogeochemistry, 77, 265281.CrossRefGoogle Scholar
Hori, T., Itasaka, O. and Mitamura, O., 1969. The removal of dissolved silica from freshwater in the Lake Biwa-ko. Mem. Fac. Liberal Arts Educ. Shiga Univ., 19, 4551 (in Japanese with English summary).Google Scholar
Horne, A.J. and Goldman, C.R., 1994. Phytoplankton and periphyton. In: Limnology, 2nd edn, McGraw-Hill, New York, 226264.Google Scholar
Humborg, C., Ittekkot, V., Cociasu, A. and Bodungen, B., 1997. Effect of Danube River dam on Black Sea biogeochemistry and ecosystem structure. Nature, 386, 385388.CrossRefGoogle Scholar
Humborg, C., Conley, D.J., Rahm, L., Wulff, F., Cociasu, A. and Ittekkot, V., 2000. Silicon retention in river basins: far-reaching effects on biogeochemistry and aquatic food webs in coastal marine environments. Ambio, 29, 4550.CrossRefGoogle Scholar
Kawabata, K., 1987. Ecology of large phytoplankton in Lake Biwa: population dynamics and food relations with zooplankters. Bull. Plankton Soc. Japan, 34, 165172.Google Scholar
Kawamura, S. and Goto, K., 1994. Silicate. In: The Japan Society for Analytical Chemistry, Hokkaido Branch (ed.), Mizu no bunseki, 4th edn, Kagakudojin, Kyoto, 181184 (in Japanese).Google Scholar
Menzel, D.W. and Corwin, N., 1965. The measurement of total phosphorus in seawater based on the liberation of organically bound fraction by persulfate oxidation. Limnol. Oceanogr., 10, 280282.CrossRefGoogle Scholar
Miyajima, T., Nakano, S. and Nakanishi, M., 1995. Planktonic diatoms in pelagic silicate cycle in Lake Biwa. Jpn J. Limnol., 56, 211220.CrossRefGoogle Scholar
Müller, B., Maerki, M., Schmid, M., Vologina, E.G., Wehrli, B., Wüest, A. and Sturm, M., 2005. Internal carbon and nutrient cycling in Lake Baikal: sedimentation, upwelling, and early diagenesis. Global Planet. Change, 46, 101124.CrossRefGoogle Scholar
Mullin, J.B. and Riley, J.P., 1955. The colorimetric determination of silicate with special reference to sea and natural waters. Anal. Chim. Acta, 12, 162176.CrossRefGoogle Scholar
Murphy, J. and Riley, J.P., 1962. A modified single solution method for the determination of phosphate in natural waters. Anal. Chim. Acta, 27, 3136.CrossRefGoogle Scholar
Negoro, K., 1960. Studies on the diatom-vegetation of Lake Biwa-ko. Jpn J. Limnol., 21, 200220 (in Japanese).CrossRefGoogle Scholar
Negoro, K., 1967. An analytical study of diatom shells in the bottom deposits of Lake Biwa-ko, based on a new core-sample. Jpn J. Limnol., 28, 132135 (in Japanese).CrossRefGoogle Scholar
Nixon, S.W., 2003. Replacing the Nile: are anthropogenic nutrients providing the fertility once brought to the mediterranean by a great river? Ambio, 32, 3039.CrossRefGoogle ScholarPubMed
Pilskaln, C.H., 2004. Seasonal and interannual particle export in an African rift valley lake: a 5-yr record from Lake Malawi, southern East Africa. Limnol. Oceanogr., 49, 964977.CrossRefGoogle Scholar
Poister, D. and Armstrong, D.E., 2003. Seasonal sedimentation trends in a mesotrophic lake: influence of diatoms and implications for phosphorus dynamics. Biogeochemistry, 65, 113.CrossRefGoogle Scholar
Ragueneau, O., Tréguer, P., Leynaert, A., Anderson, R.F., Brzezinski, M.A., DeMaster, D.J., Dugdale, R.C., Dymond, J., Fischer, G., François, R., Heinze, C., Maier-Reimer, E., Martin-Jézéquel, V., Nelson, D.M. and Quéguiner, B., 2000. A review of the Si cycle in the modern ocean: recent progress and missing gaps in the application of biogenic opal as a paleoproductivity proxy. Global Planet. Change, 26, 317365.CrossRefGoogle Scholar
Ryves, D.B., Jewson, D.H., Sturm, M., Battarbee, R.W., Flower, R.J., Mackay, A.W. and Granin, N.G., 2003. Quantitative and qualitative relationships between planktonic diatom communities and diatom assemblages in sedimenting material and surface sediments in Lake Bikal, Siberia. Limnol. Oceanogr., 48, 16431661.CrossRefGoogle Scholar
Sagi, T., 1966. Determination of ammonia in sea water by the indophenol method and its application to the coastal and off-shore waters. Oceanograph. Mag., 18, 4351.Google Scholar
Saxton, M.A., D'souza, N.A., Bourbonniere, R.A., McKay, R.M.L. and Wilhelm, S.W., 2012. Seasonal Si:C ratios in Lake Erie diatoms — evidence of an active winter diatom community. J. Great Lakes Res., 38, 206211.CrossRefGoogle Scholar
Schelske, C.L. and Stoermer, E.F., 1971. Eutrophication, silica depletion, and predicted changes in algal quality in Lake Michigan. Science, 173, 423424.CrossRefGoogle ScholarPubMed
Schelske, C.L. and Stoermer, E.F., 1972. Phosphorus, silica and eutrophication in Lake Michigan. In: Likens, G.E. (ed.), Nutrients and Eutrophication. American Society of Limnology and Oceanography, Kansas, 157171.Google Scholar
Schelske, C.L., Eadie, B.J. and Krausse, G.I., 1984. Measured and predicted fluxes of biogenic silica in Lake Michigan. Limnol. Oceanogr., 29, 99110.CrossRefGoogle Scholar
Schreiber, U., Hormann, H., Neubauer, C. and Klughammer, C., 1995. Assessment of photosystem II photochemical quantum yield by chlorophyll fluorescence quenching analysis. Aust. J. Plant. Physiol., 22, 209220.CrossRefGoogle Scholar
Sferratore, A., Billen, G., Garnier, J., Smedberg, E., Humborg, C. and Rahm, L., 2008. Modelling nutrient fluxes from sub-arctic basins: comparison of pristine vs. dammed rivers. J. Mar. Syst., 73, 236249.CrossRefGoogle Scholar
Sicko-Goad, L.M., Schelske, C.L. and Stoermer, E.F., 1984. Estimation of intracellular carbon and silica content of diatoms from natural assemblages using morphometric techniques. Limonol. Oceanogr., 29, 11701178.CrossRefGoogle Scholar
Teubner, K. and Dokulil, M.T., 2002. Ecological stoichiometry of TN: TP: SRSi in freshwaters: nutrient ratios and seasonal shifts in phytoplankton assemblages. Arch. Hydrobiol., 154, 625646.CrossRefGoogle Scholar
Tezuka, Y., 1984. Seasonal variations of dominant phytoplankton, chlorophyll a and nutrient levels in the pelagic regions of Lake Biwa. Jap. J. Limnol., 45, 2637.CrossRefGoogle Scholar
Turner, R.E., Rabalais, N.N., Justic, D. and Dortch, Q., 2003. Global patterns of dissolved N, P and Si in large Rivers. Biogeochemistry, 64, 297317.CrossRefGoogle Scholar
Wetzel, R.G., 2001. Iron, sulfur, and silica cycles. In: Limnology–Lake and River Ecosystems–, Academic Press, San Diego, 289330.Google Scholar