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Sunlight-induced carbon dioxide emissions from inland waters

机译:阳光引起的内陆水域二氧化碳排放

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The emissions of carbon dioxide (CO_2) from inland waters are substantial on a global scale. Yet the fundamental question remains open which proportion of these CO_2 emissions is induced by sunlight via photochemical mineralization of dissolved organic carbon (DOC), rather than by microbial respiration during DOC decomposition. Also, it is unknown on larger spatial and temporal scales how photochemical mineralization compares to other C fluxes in the inland water C cycle. We combined field and laboratory data with atmospheric radiative transfer modeling to parameterize a photochemical rate model for each day of the year 2009, for 1086 lakes situated between latitudes from 55°N to 69°N in Sweden. The sunlight-induced production of dissolved inorganic carbon (DIC) averaged 3.8 ± 0.04 g C m~(-2) yr~(-1), which is a flux comparable in size to the organic carbon burial in the lake sediments. Countrywide, 151 ± 1 kt C yr~(-1) was produced by photochemicalmineralization, corresponding to about 12% of total annual mean CO_2 emissions fromSwedish lakes. With amedian depth of 3.2m, the lakes were generally deep enough that incoming, photochemically active photons were absorbed in the water column. This resulted in a linear positive relationship between DIC photoproduction and the incoming photon flux,which corresponds to the absorbed photons. Therefore, the slope of the regression line represents the wavelength- and depth-integrated apparent quantum yield of DIC photoproduction. We used this relationship to obtain a first estimate of DIC photoproduction in lakes and reservoirs worldwide. Global DIC photoproduction amounted to 13 and 35 Mt C yr~(-1) under overcast and clear sky, respectively. Consequently, these directly sunlight-induced CO_2 emissions contribute up to about one tenth to the global CO_2 emissions from lakes and reservoirs, corroborating that microbial respiration contributes a substantially larger share than formerly thought, and generate annual C fluxes similar in magnitude to the C burial in natural lake sediments worldwide.
机译:在全球范围内,内陆水域的二氧化碳排放量很大。然而,仍然存在一个基本问题,即这些CO_2排放的哪部分是由阳光通过溶解有机碳(DOC)的光化学矿化而不是由DOC分解过程中的微生物呼吸引起的。同样,在更大的时空尺度上,内陆水碳循环中光化学矿化与其他碳通量的比较是未知的。我们将现场和实验室数据与大气辐射传输模型相结合,以参数化2009年每一天的光化学速率模型,该模型适用于瑞典北纬55°至69°N之间的1086个湖泊。阳光诱导的溶解性无机碳(DIC)的平均产量为3.8±0.04 g C m〜(-2)yr〜(-1),该通量的大小与湖泊沉积物中的有机碳埋葬相当。在全国范围内,通过光化学矿化产生了151±1 kt C yr〜(-1),约占瑞典湖泊年平均CO_2排放总量的12%。湖泊的中间深度为3.2m,通常足够深,以至进入的光化学活性光子在水柱中被吸收。这导致DIC光产生与入射光子通量之间线性正相关,入射光子通量与吸收的光子相对应。因此,回归线的斜率表示DIC光生产的波长和深度积分的表观量子产率。我们使用这种关系来获得对全球湖泊和水库中DIC光产生的初步估计。在多云和晴朗的天空下,全球DIC的照相产量分别为13 Mt C yr〜(-1)。因此,这些直接的阳光诱导的CO_2排放量占湖泊和水库的全球CO_2排放量的十分之一左右,这证实了微生物呼吸作用比以前认为的要大得多,并且产生的年度C通量的大小与C埋葬相似。遍布全球的天然湖泊沉积物中。

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