Pan Gang, Krom Michael D, Herut Barak
State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing.
Environ Sci Technol. 2002 Aug 15;36(16):3519-24. doi: 10.1021/es020516d.
The potential importance of adsorption-desorption behavior of phosphorus (P) on the East Mediterranean (E. Med) P cycle was investigated. Contrasting adsorption behavior between Saharan dust (SD) and Nile particulate matter (Nile PM) was observed. SD was a source of P to the region, which released an average of 3.3 +/- 0.3 micromolP/g into the surface seawater and showed no adsorption ability under the conditions close to the E. Med deep water. Saharan dust is therefore unlikely to be the reason for P limitation in the region. By contrast, Nile PM acted dual roles of a sink and source of P in different waters (surface seawater, deep seawater, and river water). A new crossover-type adsorption-desorption model explained the contrasting adsorption behavior and the dual nature of natural particles. The model indicates that when natural particles are transported between different waters, they can be a sink (adsorption) or a source (desorption) of phosphorus depending on the "specific concentration (lambda)", which is the ratio between the aqueous P concentration and the zero equilibrium P concentration (EPC0). EPC0 refers to the solute concentration value where the adsorption isotherm crosses over the aqueous concentration axis. When lambda > 1, adsorption occurs, whereas when lambda < 1, desorption occurs. The model added a general development to the methodology of adsorption isotherm, where, for the first time, effects of solute concentration, solid concentration, and aqueous medium (EPC0) on the adsorption and desorption of P in natural waters were simultaneously described by a single equation. Using the model, it was quantitatively reconstructed that particles emitted during the pre-1964 Nile floods could be a major source of P to Egyptian coastal waters (up to 4800 tonsP/yr), greater than the dissolved P flux (approximately 3200 tonsP/yr), but a trapper of dissolved phosphate in E. Med deep waters.
研究了磷(P)的吸附-解吸行为对东地中海(E. Med)磷循环的潜在重要性。观察到撒哈拉沙尘(SD)和尼罗河颗粒物(尼罗河PM)之间存在对比鲜明的吸附行为。SD是该区域的磷源,平均向表层海水中释放3.3±0.3 μmolP/g,并且在接近东地中海深水的条件下没有吸附能力。因此,撒哈拉沙尘不太可能是该区域磷限制的原因。相比之下,尼罗河PM在不同水体(表层海水、深层海水和河水)中扮演着磷的汇和源的双重角色。一个新的交叉型吸附-解吸模型解释了天然颗粒这种对比鲜明的吸附行为和双重性质。该模型表明,当天然颗粒在不同水体之间运输时,它们可以是磷的汇(吸附)或源(解吸),这取决于“比浓度(λ)”,即水体中磷浓度与零平衡磷浓度(EPC0)的比值。EPC0是指吸附等温线与水体浓度轴相交处的溶质浓度值。当λ>1时,发生吸附,而当λ<1时,发生解吸。该模型为吸附等温线方法增添了一项一般性进展,首次通过一个单一方程同时描述了溶质浓度、固体浓度和水体介质(EPC0)对天然水体中磷吸附和解吸的影响。利用该模型进行定量重建发现,1964年以前尼罗河洪水期间排放的颗粒可能是埃及沿海水体磷的主要来源(高达4800吨P/年),大于溶解态磷通量(约3200吨P/年),但却是东地中海深水中溶解态磷酸盐的捕获者。