Soil CO2 dynamics, acidification, and chemical weathering in a temperate forest with experimental CO2 enrichment

被引:246
作者
Andrews, JA
Schlesinger, WH
机构
[1] Duke Univ, Nicholas Sch Environm, Dept Bot, Durham, NC 27708 USA
[2] Duke Univ, Nicholas Sch Environm, Div Earth & Ocean Sci, Durham, NC 27708 USA
关键词
D O I
10.1029/2000GB001278
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Soils constitute a major component of the global carbon cycle that will be affected by anthropogenic additions of CO2 to the atmosphere. As part of the Duke Forest Free-Air CO2 Enrichment (FACE) experiment, we examined how forest growth at elevated (+200 ppmv) atmospheric CO2 concentration affects CO2 dynamics in the soil. Soil respiration and the concentration of CO2 the soil pore space to a depth of 200 cm were measured over a 3-year period. Soil CO2 production was linked to soil acidification and mineral weathering by measuring changes in the composition of the soil solution, including alkalinity, Si, and major cations. The total flux of dissolved inorganic carbon to groundwater was then calculated from field measurements. The FACE fumigation gas contained a unique C-13 signature that labeled newly fixed carbon, which was monitored in the soil system. As a result of CO2 enrichment, annual soil respiration increased by 27% and was accompanied by higher CO2 concentrations in the soil pore space. These changes to soil CO2 dynamics were most likely the result of increased root and rhizosphere respiration, as suggested by the changes to the delta C-13 of soil CO2. Increased soil CO2 under FACE accelerated the rates of soil acidification and mineral weathering. Thus an increase of 55% in atmospheric CO2 concentration over 2 years resulted in a 271% increase in soil solution cation concentration, a 162% increase in alkalinity and a 25% increase in Si concentration at 200-cm depth. The flux of dissolved inorganic carbon to groundwater increased by 33%, indicating a negative feedback to changes in atmospheric CO2 that could regulate the global carbon cycle over geological time.
引用
收藏
页码:149 / 162
页数:14
相关论文
共 101 条
[11]  
Berner RA, 1995, REV MINERAL, V31, P565
[12]   THE CARBONATE-SILICATE GEOCHEMICAL CYCLE AND ITS EFFECT ON ATMOSPHERIC CARBON-DIOXIDE OVER THE PAST 100 MILLION YEARS [J].
BERNER, RA ;
LASAGA, AC ;
GARRELS, RM .
AMERICAN JOURNAL OF SCIENCE, 1983, 283 (07) :641-683
[13]   Paleoclimate - The rise of plants and their effect on weathering and atmospheric CO2 [J].
Berner, RA .
SCIENCE, 1997, 276 (5312) :544-546
[14]  
Berner RA, 1996, AQUAT GEOCHEM, V2, P301
[15]   Roots exert a strong influence on the temperature sensitivity of soil respiration [J].
Boone, RD ;
Nadelhoffer, KJ ;
Canary, JD ;
Kaye, JP .
NATURE, 1998, 396 (6711) :570-572
[16]   Rapid, plant-induced weathering in an aggrading experimental ecosystem [J].
Bormann, BT ;
Wang, D ;
Bormann, FH ;
Benoit, G ;
April, R ;
Snyder, MC .
BIOGEOCHEMISTRY, 1998, 43 (02) :129-155
[17]  
BOUTTON T W, 1991, P155
[18]   DIRECT EFFECTS OF CO2 AND TEMPERATURE ON SILICATE WEATHERING - POSSIBLE IMPLICATIONS FOR CLIMATE CONTROL [J].
BRADY, PV ;
CARROLL, SA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1994, 58 (07) :1853-1856
[19]   Does atmospheric CO2 police the rate of chemical weathering? [J].
Broecker, WS ;
Sanyal, A .
GLOBAL BIOGEOCHEMICAL CYCLES, 1998, 12 (03) :403-408
[20]   ON THE TEMPERATURE-DEPENDENCE OF MINERAL DISSOLUTION RATES [J].
CASEY, WH ;
SPOSITO, G .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1992, 56 (10) :3825-3830