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Changes to belowground carbon dioxide dynamics under experimental CO(2) enrichment of a forest ecosystem.

机译:在森林生态系统的实验性CO(2)富集下地下二氧化碳动力学的变化。

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Forest soils constitute a major component of the global carbon cycle. It is likely that increasing atmospheric CO2 as a result of human activity is having a significant effect on soil carbon cycling, and may result in the formation of a long-term sink for excess atmospheric carbon. As part of the Duke Forest Free-Air CO2 Enrichment (FACE) experiment, the effect of a 50% increase in atmospheric CO2 concentration on CO2 dynamics in a loblolly pine (Pinus taeda L.) forest soil was examined.; Soil respiration and the concentration of CO2 in the soil pore space to a depth of 200 cm were measured over a three year period. The d13C of organic carbon in this soil and of soil-respired CO2 was monitored and used to determine the origin of the CO2 in the soil system. Soil solution chemistry, including total cation concentration and alkalinity, was measured and used to calculate the total flux of dissolved inorganic carbon to groundwater. The size and isotopic composition of labile soil carbon pools in the organic horizon and in the surface mineral soil were determined throughout the experiment.; The experimental increase in atmospheric CO2 caused total annual carbon flux from the soil to the atmosphere to increase by 27% and the instantaneous rate of soil respiration to increase by up to 131%. The greater soil respiration was accompanied by higher CO2 concentrations in the soil pore space which, in turn, accelerated the rates of soil acidification and mineral weathering. In soil solution from 200-cm depth, cation concentrations increased by 286% and alkalinity increased by 164%. As a result, there was a 33% greater flux of dissolved inorganic carbon to groundwater under high atmospheric CO2. These changes to soil CO2 dynamics were attributed to increased root and rhizosphere respiration. A shift in the d13C of soil CO2 indicated that root activity contributed 55% of soil respiration at the site and decreased with increasing soil depth. The d13C of soil-respired CO2 was also found be to affected by soil temperature. There was no detectable change to the size of the organic horizon or the pool of labile carbon in the mineral soil. The change in the d13C of these pools under FACE indicated that the mean residence time was 3 and 4 to 6 years, respectively. These results suggest that high atmospheric CO2 increases the fluxes of inorganic carbon in the soil system but may have relatively little effect on soil carbon storage.
机译:森林土壤是全球碳循环的主要组成部分。由于人类活动而增加的大气CO2可能对土壤碳循环产生重大影响,并可能导致形成过量碳的长期汇。作为杜克森林自由空气二氧化碳富集(FACE)实验的一部分,研究了大气二氧化碳浓度增加50%对火炬松(Pinus taeda L.)森林土壤中二氧化碳动态的影响。在三年的时间内测量了土壤呼吸和土壤孔隙中200 cm深度的CO2浓度。监测该土壤和土壤呼吸的CO2中的有机碳d13C,并将其用于确定土壤系统中CO2的来源。测量了土壤溶液的化学成分,包括总阳离子浓度和碱度,并将其用于计算溶解的无机碳向地下水的总通量。在整个实验过程中,确定了有机层和表层矿物土壤中不稳定土壤碳库的大小和同位素组成。大气中二氧化碳的实验性增加导致从土壤到大气的年总碳通量增加了27%,土壤呼吸的瞬时速率增加了高达131%。较大的土壤呼吸作用伴随着土壤孔隙空间中较高的CO2浓度,进而加快了土壤酸化和矿物风化的速度。在200厘米深的土壤溶液中,阳离子浓度增加了286%,碱度增加了164%。结果,在高大气CO2下,溶解的无机碳向地下水的通量增加了33%。这些土壤二氧化碳动态的变化归因于根和根际呼吸的增加。土壤二氧化碳的d13C值的变化表明,根系活动贡献了该地点土壤呼吸的55%,并且随着土壤深度的增加而降低。还发现土壤呼吸的二氧化碳的d13C受土壤温度的影响。矿物土壤中有机层或不稳定碳库的大小没有可检测到的变化。这些池的d13C在FACE下的变化表明平均停留时间分别为3年和4至6年。这些结果表明,较高的大气CO2会增加土壤系统中无机碳的通量,但对土壤碳储量的影响相对较小。

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