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CO_2 partial pressure and CO_2 emission in the Lower Mekong River

机译:湄公河下游的CO_2分压和CO_2排放

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CO_2 evasion from freshwaters is recently included in assessing global carbon budgets, while large uncertainty of global estimates results from incomplete spatial coverage of aquatic carbon emission. Here we examined the dissolved inorganic carbon (DIC) and carbon dioxide partial pressure (pCO_2) in riverine water from historical records at 46 stations for the period 1972-1998 in the Lower Mekong River (LMR). The river system presented an exceptional temporal and spatial variability of dissolved inorganic carbon (DIC) species. The alkalinity concentration of the LMR varied from 687 to 3189μeq/l with an average of 1524μeq/l (median value: 1586μeq/l), 1.2 times the global median value. Spatial patterns showed diminishing alkalinity downstream at the main-channel stations along the LMR. Similar to many other Himalayan rivers, alkalinity varied seasonally and inversely related to river runoff with a variation factor of 1.2-1.6, despite a water dilution of 7-fold to 13-fold in the summer flood season. The pCO_2 levels ranged from 224 to 5970μatm with a total average of 1090μatm and obvious monthly and spatial variations. Under-saturated pCO_2 samples (<390μatm) primarily occurred in the high-flow period. pCO_2 at the main-channel stations increased downstream and averaged from 720μatm (Mukdahan) to 1670μatm (Can Tho). Calculated water-to-air CO_2 degassing from the Mekong River was 71mol/m~2/yr, thus 6.8Tg C/yr as CO_2 was released to the atmosphere, 1.5-fold the sea-ward DIC export (4.5Tg C/yr). Basin characteristics influences on pCO_2 from 25 global rivers demonstrated that non-carbonate rocks significantly contributed to pCO_2, population density, agricultural practices, elevation and slope decreased pCO_2, while forest significantly increased pCO_2. Our results demonstrated the essential need to consider river water area as an essential atmospheric CO_2 source, albeit this atmospheric flux, representing significant riverine carbon budgets, was highly variable at temporal and spatial scales.
机译:近来从淡水中逃逸的CO_2已包括在评估全球碳预算中,而全球估算的较大不确定性是由于水生碳排放的空间覆盖不完整造成的。在这里,我们根据湄公河下游(LMR)1972-1998年期间46个站点的历史记录,检查了河水中的溶解性无机碳(DIC)和二氧化碳分压(pCO_2)。河流系统呈现出异常的溶解无机碳(DIC)物种的时空变化。 LMR的碱度浓度从687到3189μeq/ l不等,平均值为1524μeq/ l(中值:1586μeq/ l),是全球中值的1.2倍。空间格局显示,沿LMR的主河道站下游的碱度降低。与许多其他喜马拉雅河流域相似,碱度随季节而变化,与河流径流成反比,变化系数为1.2-1.6,尽管夏季汛期的水稀释度为7到13倍。 pCO_2的水平范围为224〜5970μatm,总平均值为1090μatm,并且每月和空间都有明显的变化。饱和度较低的pCO_2样品(<390μatm)主要发生在高流量时期。主通道站的pCO_2向下游增加,平均从720μatm(Mukdahan)增加到1670μatm(Can Tho)。据计算,从湄公河脱气的水对空气CO_2为71mol / m〜2 / yr,因此当CO_2释放到大气中时为6.8Tg C / yr,是沿海DIC出口量的1.5倍(4.5Tg C / yr) )。流域特征对全球25条河流的pCO_2的影响表明,非碳酸盐岩对pCO_2,人口密度,农业实践,海拔和坡度降低的pCO_2均有显着贡献,而森林对pCO_2的影响显着。我们的结果表明,将河流水域视为一种重要的大气CO_2来源是至关重要的,尽管代表河流中大量碳预算的这种大气通量在时间和空间尺度上变化很大。

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