Evaluation of iron-phosphate as a source of internal lake phosphorus loadings

Biological, physical and chemical characteristics of the water column of a shallow (z(max) = 9.2 m), small (surface area 3.8 km(2)) residential and recreational lake near Prince George, British Columbia, indicated that the system was being loaded internally with phosphorus (P) from the sediments. The abundance of P released from the fine glaciolacustrine, and organic rich sediments was resulting in excess algal and weed growth. It was postulated that iron-phosphate reduction at redox potentials below approximately 200 mV and/or bacterially mediated orthophosphate (PO4-P) releases could be occurring. The development of an appropriate nutrient management strategy required that the process associated with the sediment P release be determined. The MINTEQA2 geochemical model was used to predict the release of orthophosphate (PO4-P) into the interstitial water with the assumption that P is present alternately as strengite, variscite and hydroxyapatite. The predicted release of PO4-P from these P containing minerals was compared to the concentration of PO4-P and total phosphorus (TP) in the overlying hypolimnion. In order to improve the accuracy of the model prediction, the proportion of the sediment present as iron-bound phosphate was estimated. A significant correlation between the observed hypolimnetic TP and interstitial PO4-P concentrations as predicted from iron-bound P dissolution (r(2) = 0.59) was found. Total phosphorus release rates to the hypolimnion were also found to be strongly correlated to the iron-bound P component of the sediment (r(2) = 0.88). Multivariate regression analyses showed significant relationships between hypolimnetic PO4-P and sediment iron-bound P, Eh, and interstitial Fe (r(2) = 0.76). These results provided sufficient evidence to conclude that PO4-P in the system is predominantly bound to Fe-containing minerals and therefore could be managed using treatment techniques that address iron-bound phosphates. (C) 2001 Elsevier Science B.V. All rights reserved.