Contrasting the sorption of Zn by oxyhydroxides of Mn and Fe, and organic matter along a mineral-poor to mineral-rich fen gradient

被引:11
作者
Bendell-Young, L [1 ]
机构
[1] Simon Fraser Univ, Dept Biol Sci, Burnaby, BC V5A 1S6, Canada
关键词
D O I
10.1016/S0883-2927(98)00097-3
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The geochemistry of Mn and Fe in surface pools, pore-waters and surface peats and the sorption of Zn by the surface peats was contrasted among 15 peatlands sampled along a mineral-poor to mineral-rich fen gradient. Sorption of Zn by surficial peats was compared via distribution coefficients, both total (K-DT) and partial (K-DERMn, K-DRFe and K-DORG), where ER Mn, R Fe and ORG are amounts of Zn recovered from the easily reducible Mn oxides, reducible Fe oxides, and organic components of peat, respectively. Apparent stability constants (K(A)s) for Zn sorption onto oxides of Fe recovered from the surface peats were also calculated and compared along the same gradient. Feat geochemistry was peatland dependent; mineral-poor fens had less easily reducible Mn and greater amounts of organic matter (%Loss on Ignition; LOI) versus mineral-rich fens (range of 0.66-8.6 mm kg(-1) for ER Mn and 20-88% LOI for organic matter), Reducible Fe also varied among peatlands (range 51-315 mm kg(-1)) but was independent of the mineral-poor to mineral-rich fen gradient. Comparison of partial K(D)s for amounts of Zn sorped onto the ER Mn, R Fe and ORG components of peat indicated that sorption was dominated by R Fe in all peatlands. KD-rs ranged from 0.54-2.00, In contrast to other aquatic systems, however, the range in K(DT)s was not related to either surface or pore-water pH. KAs ranged from 0.35 to 3.06 and were also independent of surface or pore-water pH. However, average K(A)s (but not K(DT)s), were greater for mineral-poor fens (P < 0.02), suggesting greater Zn binding by surface peats of mineral-poor fens versus either the moderately poor or mineral-rich peatlands. Other water chemistry variables, such as pore-water base cation concentrations, weakly correlated to Zn partitioning onto R Fe (r = -0.35, P = 0.05), but did not fully explain differences in Zn partitioning among peatlands. Greater average KAs for the mineral-poor peatlands may in part be due to the presence of strong metalorganic matter-Fe oxide complexes in the Sphagnum dominated peatlands as well as lower pore-water base cation concentrations that occur in the mineral-poor peatland as compared to the more mineral-rich fens. (C) 1999 Elsevier Science Ltd. All rights reserved.
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页码:719 / 734
页数:16
相关论文
共 40 条
[1]   THE ADSORPTION OF CU, PB, ZN, AND CD ON GOETHITE FROM MAJOR ION SEA-WATER [J].
BALISTRIERI, LS ;
MURRAY, JW .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1982, 46 (07) :1253-1265
[2]   Base cation composition of pore water, peat and pool water of fifteen Ontario peatlands: Implications for peatland acidification [J].
BendellYoung, L ;
Pick, FR .
WATER AIR AND SOIL POLLUTION, 1997, 96 (1-4) :155-173
[3]   CONTRASTING THE GEOCHEMISTRY OF ALUMINUM AMONG PEATLANDS [J].
BENDELLYOUNG, L ;
PICK, FR .
WATER AIR AND SOIL POLLUTION, 1995, 81 (3-4) :219-240
[4]   CONTRASTING BEHAVIOR OF MANGANESE IN THE SURFICIAL SEDIMENTS OF 13 SOUTH-CENTRAL ONTARIO LAKES [J].
BENDELLYOUNG, LI ;
HARVEY, HH ;
DILLON, PJ ;
SCHOLER, PJ .
SCIENCE OF THE TOTAL ENVIRONMENT, 1989, 87-8 :129-139
[5]  
BENDELLYOUNG LI, 1992, LIMNOL OCEANOGR, V37, P603
[6]  
BENDELLYOUNG LI, 1992, GEOCHIM COSMOCHIM AC, V56, P1175
[7]  
BENDELLYOUNG LI, 1992, BIOGEOCHEMISTRY, V17, P15
[8]   MULTIPLE-SITE ADSORPTION OF CD, CU, ZN, AND PB ON AMORPHOUS IRON OXYHYDROXIDE [J].
BENJAMIN, MM ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1981, 79 (01) :209-221
[9]   PEATLAND WATER CHEMISTRY IN CENTRAL ONTARIO IN RELATION TO ACID DEPOSITION [J].
BLANCHER, PJ ;
MCNICOL, DK .
WATER AIR AND SOIL POLLUTION, 1987, 35 (3-4) :217-232
[10]  
Campbell P., 1988, 27694 NRCC