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Found 2 results.

Concentration data of NO3-, NH4+, PO4, and Si from filtered sediment porewaters. Basis for the flux data “F” in Table 1

Porewater samples were conserved with 0.2% chloroform and analyzed at EAWAG, Switzerland, for NO3-, NH4+, SiO2, and o-PO4 using standard photometric methods (DEW, 1996). In 2002, NH4+ in porewater was measured on board of the research vessel with the indophenol method (DEW, 1996) and a portable photometer (Merck Spectroquant). In March and July 2001, porewater measurements of O2, NO3−, and NH4+ were performed with ion-selective electrodes on retrieved sediment cores from the South Basin, Vydrino, and Posolskoe High on the ice and in the hydrological institute on shore at Listvijanka to give vertical concentration profiles with high spatial resolution. Measurements are described in detail by Maerki et al. (submitted for publication). Diffusive fluxes across the sediment–water interface were calculated from the chemical gradients of their porewater concentration profiles assuming steady-state conditions and using Ficks first law of diffusion (Berner, 1980):

The relationship between concentrations of chl-a calculated from SeaWiFS OC2 and chl-a calculated determined from ground truth measurements during field expeditions in Lake Baikal during 2001 and 2002

Values of measured chlorophyll (HPLC=High Pressure Liquid Chromatography) are the mean concentrations of each sampling point from 5 to 30 m depth. For the OC2 chl-a calculations, the least clouded acquisitions in 2001 (2001/07/19) and 2002 (2002/07/20) were chosen. Note the considerable chl-a overestimation caused by the influences of terrigenous input in case 2 waters.

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