Phosphite flux at the sediment-water interface in northern Lake Taihu

Phosphite (H2PO3(-), HPO3(2-), +3 valence), a reduced form of phosphorus (P), has been widely detected in water environments. The role of phosphite in the P biogeochemical cycle has not been investigated systematically and quantitative results on phosphite fluxes are lacking. In this study, intact sediment core simulation was employed to measure the flux of phosphite at the sediment-water interface in northern Lake Taihu. Phosphite fluxes (μmol m(-2) d(-1)) ranged from -38.21±1.14 to 7.10±2.18, with an annual average of -4.72±10.40. On the whole, phosphite migrated from water into sediment and the sediment was primarily a sink. The highest seasonal negative phosphite fluxes (μmol m(-2) d(-1)) occurred in winter (-10.44±18.63), followed by summer (-8.04±5.61) and spring (-2.61±4.17). In autumn, phosphite flux was 2.20±4.07. Higher annual average negative fluxes of phosphite (μmol m(-2) d(-1)) appeared in site ZSB (-12.70±17.96), which contained the highest content of total soluble P. The average yearly migration of phosphite in Lake Taihu from water to sediment was estimated to be (4.04±8.88)×10(6) mol y(-1). The transfer of phosphite from water into sediment usually occurs in winter may due to the season's natural tendency to create more favorable conditions for phosphite biogeochemical reactions. Phosphite fluxes showed significant negative correlations with the original phosphite concentration in water (r=-0.840, p<0.01), as well as organic matter (r=-0.720, p<0.01) and phosphate bound to Ca (Ca-Ps) (r=-0.632, p<0.05) in sediment. These results indicate that microbiological processes and P species bound to Ca may play an important role in the P redox cycle. No significant correlations between phosphite fluxes and dissolved oxygen or oxidation-reduction potential were observed.