National Oceanography Centre, Southampton, UK.
British Geological Survey, Wallingford, UK.
Sci Total Environ. 2018 Jul 15;630:630-647. doi: 10.1016/j.scitotenv.2018.02.237. Epub 2018 Feb 27.
The flow of terrestrial carbon to rivers and inland waters is a major term in the global carbon cycle. The organic fraction of this flux may be buried, remineralized or ultimately stored in the deep ocean. The latter can only occur if terrestrial organic carbon can pass through the coastal and estuarine filter, a process of unknown efficiency. Here, data are presented on the spatial distribution of terrestrial fluorescent and chromophoric dissolved organic matter (FDOM and CDOM, respectively) throughout the North Sea, which receives organic matter from multiple distinct sources. We use FDOM and CDOM as proxies for terrestrial dissolved organic matter (tDOM) to test the hypothesis that tDOM is quantitatively transferred through the North Sea to the open North Atlantic Ocean. Excitation emission matrix fluorescence and parallel factor analysis (EEM-PARAFAC) revealed a single terrestrial humic-like class of compounds whose distribution was restricted to the coastal margins and, via an inverse salinity relationship, to major riverine inputs. Two distinct sources of fluorescent humic-like material were observed associated with the combined outflows of the Rhine, Weser and Elbe rivers in the south-eastern North Sea and the Baltic Sea outflow to the eastern central North Sea. The flux of tDOM from the North Sea to the Atlantic Ocean appears insignificant, although tDOM export may occur through Norwegian coastal waters unsampled in our study. Our analysis suggests that the bulk of tDOM exported from the Northwest European and Scandinavian landmasses is buried or remineralized internally, with potential losses to the atmosphere. This interpretation implies that the residence time in estuarine and coastal systems exerts an important control over the fate of tDOM and needs to be considered when evaluating the role of terrestrial carbon losses in the global carbon cycle.
陆地碳向河流和内陆水域的流动是全球碳循环的一个主要因素。该通量的有机部分可能被埋藏、再矿化或最终储存在深海中。只有当陆地有机碳能够通过沿海和河口过滤器时,后者才会发生,而这个过程的效率是未知的。在这里,我们提供了整个北海中陆地荧光和有色溶解有机物(FDOM 和 CDOM,分别)的空间分布数据,这些有机物来自多个不同的来源。我们使用 FDOM 和 CDOM 作为陆地溶解有机物(tDOM)的替代品,以检验 tDOM 是否通过北海定量传递到开阔的北大西洋的假设。激发发射矩阵荧光和平行因子分析(EEM-PARAFAC)揭示了单一的陆地腐殖质类化合物,其分布仅限于沿海边缘,并通过与盐度的反比关系,与主要的河流输入有关。在东南北海的莱茵河、威悉河和易北河的联合流出物以及波罗的海流向北海中部的东部出口处,观察到两种不同来源的荧光腐殖质类物质。从北海向大西洋输送的 tDOM 通量似乎微不足道,尽管我们的研究没有采样挪威沿海水域,可能会发生 tDOM 输出。我们的分析表明,从西北欧和斯堪的纳维亚大陆出口的大部分 tDOM 被埋藏或内部再矿化,可能会损失到大气中。这种解释意味着在河口和沿海系统中的停留时间对 tDOM 的命运起着重要的控制作用,在评估陆地碳损失在全球碳循环中的作用时需要考虑这一点。