Denitrification and mixing in a schist aquifer: influence on water chemistry and isotopes

被引:102
作者
Pauwels, H [1 ]
Foucher, JC [1 ]
Kloppmann, W [1 ]
机构
[1] Bur Rech Geol & Minieres, F-45060 Orleans, France
关键词
nitrate; denitrification; pyrite; isotopes; schist aquifer;
D O I
10.1016/S0009-2541(00)00201-1
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
Nitrate concentrations in groundwater close to the water table in the upper weathered zone of the Coet-Dan catchment (Brittany, France) reach 200 mg/l. With intensive agriculture covering 86.5% of the catchment area, the pollution results principally from the spreading of livestock manure. The rapid decrease of NO3- concentrations with depth in the fractured part of the aquifer is partly the result of dilution by older groundwater that was probably never polluted, as deduced from the isotopic data of water (H-3, delta(2)H, delta(18)O) and sulphate (delta(34)S, delta(18)O) molecules. However, the extent of denitrification is demonstrated by N-2 concentrations, as well as by mass balance calculations showing that denitrification may contribute to a loss of at least 50-70 mg l(-1) of NO3- just below the upper zone of the aquifer. Several electron donors may be involved in the denitrification reactions; for example, ferrous iron and sulphides of the pyrite and organic matter, with at least the last two processes being aided by the presence of bacteria. Autotrophic denitrification is considered to be the predominant process in the unweathered schist, whereas heterotrophic processes may occur in the overlying weathered zone. Autotrophic reactions tend to liberate SO4, but concentrations of sulphate are probably controlled by precipitation of sulphate amorphous phases and also minerals such as jarosite. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:307 / 324
页数:18
相关论文
共 43 条
[1]   Solubility of jarosite at 4-35 degrees C [J].
Baron, D ;
Palmer, CD .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (02) :185-195
[2]  
BOTTCHER J, 1992, PROGR HYDROGEOCHEMIS, P219
[3]  
BRGM IRD UPMC I, 1999, 2 C GEOFCAN ORL FRAN, P105
[4]  
Cann C., 1998, AGR INTENSIVE QUALIT, P25
[5]  
CANN C, 1994, SUIVI QUALITE EAU ET
[6]  
Clarck I., 1997, ENV ISOTOPES HYDROGE
[7]  
CLAUS G, 1985, APPL MICROBIOL BIOT, V22, P283
[8]   THE AGE CURVES OF SULFUR AND OXYGEN ISOTOPES IN MARINE SULFATE AND THEIR MUTUAL INTERPRETATION [J].
CLAYPOOL, GE ;
HOLSER, WT ;
KAPLAN, IR ;
SAKAI, H ;
ZAK, I .
CHEMICAL GEOLOGY, 1980, 28 (3-4) :199-260
[9]   REDUCTION OF WATER WITH ZINC FOR HYDROGEN ISOTOPE ANALYSIS [J].
COLEMAN, ML ;
SHEPHERD, TJ ;
DURHAM, JJ ;
ROUSE, JE ;
MOORE, GR .
ANALYTICAL CHEMISTRY, 1982, 54 (06) :993-995
[10]   THE LINCOLNSHIRE LIMESTONE - HYDROGEOCHEMICAL EVOLUTION OVER A 10-YEAR PERIOD [J].
EDMUNDS, WM ;
WALTON, NRG .
JOURNAL OF HYDROLOGY, 1983, 61 (1-3) :201-211