National Oceanography Centre, University of Southampton Waterfront Campus, European Way, Southampton, SO14 3ZH, United Kingdom; Ocean and Earth Science, National Oceanography Centre Southampton, University of Southampton, Southampton, SO14 3ZH, United Kingdom; and
National Oceanography Centre, University of Southampton Waterfront Campus, European Way, Southampton, SO14 3ZH, United Kingdom;
Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):1089-94. doi: 10.1073/pnas.1415311112. Epub 2015 Jan 5.
The biological carbon pump, which transports particulate organic carbon (POC) from the surface to the deep ocean, plays an important role in regulating atmospheric carbon dioxide (CO2) concentrations. We know very little about geographical variability in the remineralization depth of this sinking material and less about what controls such variability. Here we present previously unpublished profiles of mesopelagic POC flux derived from neutrally buoyant sediment traps deployed in the North Atlantic, from which we calculate the remineralization length scale for each site. Combining these results with corresponding data from the North Pacific, we show that the observed variability in attenuation of vertical POC flux can largely be explained by temperature, with shallower remineralization occurring in warmer waters. This is seemingly inconsistent with conclusions drawn from earlier analyses of deep-sea sediment trap and export flux data, which suggest lowest transfer efficiency at high latitudes. However, the two patterns can be reconciled by considering relatively intense remineralization of a labile fraction of material in warm waters, followed by efficient downward transfer of the remaining refractory fraction, while in cold environments, a larger labile fraction undergoes slower remineralization that continues over a longer length scale. Based on the observed relationship, future increases in ocean temperature will likely lead to shallower remineralization of POC and hence reduced storage of CO2 by the ocean.
生物碳泵将颗粒有机碳 (POC) 从表层输送到深海,在调节大气二氧化碳 (CO2) 浓度方面发挥着重要作用。我们对这种下沉物质再矿化深度的地理变异性知之甚少,对控制这种变异性的因素知之更少。在这里,我们展示了以前未发表的从中层水沉降陷阱中获得的北大西洋中层水 POC 通量剖面,从中我们计算了每个站点的再矿化长度尺度。将这些结果与北太平洋的相应数据相结合,我们表明,垂直 POC 通量衰减的观测变异性可以很大程度上用温度来解释,较温暖的水域中再矿化的程度较浅。这似乎与从深海沉积物陷阱和出口通量数据分析中得出的结论不一致,这些结论表明在高纬度地区转移效率最低。然而,通过考虑温暖水域中物质易变部分的相对强烈再矿化,随后是剩余难处理部分的有效向下转移,而在寒冷环境中,较大的易变部分经历较慢的再矿化,这可以解释两种模式之间的矛盾。在较长的尺度上继续进行。基于观察到的关系,未来海洋温度的升高可能导致 POC 的再矿化变浅,从而减少海洋对 CO2 的储存。