Phosphate exchange across the sediment-water interface when shifting from anoxic to oxic conditions - an experimental comparison of freshwater and brackish-marine systems

被引:155
作者
Gunnars, A
Blomqvist, S
机构
[1] UNIV STOCKHOLM,DEPT SYST ECOL,SECT MARINE ECOL,S-10691 STOCKHOLM,SWEDEN
[2] UNIV STOCKHOLM,DEPT GEOL & GEOCHEM,S-10691 STOCKHOLM,SWEDEN
[3] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT PHYS INORGAN & STRUCT CHEM,S-10691 STOCKHOLM,SWEDEN
关键词
phosphate; iron; manganese; sediment-water exchange; limiting nutrients;
D O I
10.1023/A:1005744610602
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Comparative, experimental studies on sediment cores from freshwater and brackish-marine conditions reveal major differences in the benthic exchange of phosphate across the sediment-water interface when shifting from anoxic to oxic conditions. The flux of phosphate to the sediment during this shift was found to be mediated mainly by scavenging from newly formed colloidal ferric oxohydroxide. The capacity of the iron-rich particles to scavenge phosphorus depended on the stoichiometric ratio between dissolved iron and phosphorus built up in the supernatant water during reducing conditions. The freshwater system was characterized by high iron to phosphorus ratios in the dissolved phase and thus most of the phosphate was incorporated into the colloidal iron oxohydroxide during the oxygenation. In contrast, the marine systems reached lower iron to phosphorus ratios during the anoxic period which resulted in less efficient phosphate scavenging. Consequently, significant amounts of phosphate remained dissolved in the marine systems after the change to oxic conditions, possibly increasing the proportion of phosphate recycled to the euphotic zone. Manganese showed a consistent redox-dependent behaviour in all the investigated systems, but interacted neither with phosphate nor with iron.
引用
收藏
页码:203 / 226
页数:24
相关论文
共 118 条
[1]  
Ankar S., 1976, Contributions Asko Lab, VNo. 11, P1
[2]  
ANKAR S, 1975, JULK HAVSFORSKNINGSI, V239, P257
[3]  
[Anonymous], 1985, ANTARCTIC NUTR CYCLE
[4]   KINETICS OF ISOTOPIC-EXCHANGE OF PHOSPHATE AT ALPHA-FEOOH-AQUEOUS SOLUTION INTERFACE [J].
ATKINSON, RJ ;
QUIRK, JP ;
POSNER, AM .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1972, 34 (07) :2201-&
[5]   INFRARED STUDY OF PHOSPHATE ADSORPTION ON GOETHITE [J].
ATKINSON, RJ ;
PARFITT, RL ;
SMART, RS .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1974, 70 (08) :1472-1479
[8]  
BALZER W, 1983, OCEANOL ACTA, V6, P337
[9]  
BALZER W, 1980, NATO C SER, V4, P659
[10]   SAMPLING AND STORAGE OF NATURAL-WATERS FOR TRACE-METAL ANALYSIS [J].
BATLEY, GE ;
GARDNER, D .
WATER RESEARCH, 1977, 11 (09) :745-756