Oceanographic and Atmospheric Sciences Division, Brookhaven National Laboratory, 11973, Upton, NY, USA.
Photosynth Res. 1994 Mar;39(3):235-58. doi: 10.1007/BF00014586.
Phytoplankton biomass in the world's oceans amounts to only ∽1-2% of the total global plant carbon, yet these organisms fix between 30 and 50 billion metric tons of carbon annually, which is about 40% of the total. On geological time scales there is profound evidence of the importance of phytoplankton photosynthesis in biogeochemical cycles. It is generally assumed that present phytoplankton productivity is in a quasi steady-state (on the time scale of decades). However, in a global context, the stability of oceanic photosynthetic processes is dependent on the physical circulation of the upper ocean and is therefore strongly influenced by the atmosphere. The net flux of atmospheric radiation is critical to determining the depth of the upper mixed layer and the vertical fluxes of nutrients. These latter two parameters are keys to determining the intensity, and spatial and temporal distributions of phytoplankton blooms. Atmospheric radiation budgets are not in steady-state. Driven largely by anthropogenic activities in the 20th century, increased levels of IR- absorbing gases such as CO2, CH4 and CFC's and NOx will potentially increase atmospheric temperatures on a global scale. The atmospheric radiation budget can affect phytoplankton photosynthesis directly and indirectly. Increased temperature differences between the continents and oceans have been implicated in higher wind stresses at the ocean margins. Increased wind speeds can lead to higher nutrient fluxes. Throughout most of the central oceans, nitrate concentrations are sub-micromolar and there is strong evidence that the quantum efficiency of Photosystem II is impaired by nutrient stress. Higher nutrient fluxes would lead to both an increase in phytoplankton biomass and higher biomass-specific rates of carbon fixation. However, in the center of the ocean gyres, increased radiative heating could reduce the vertical flux of nutrients to the euphotic zone, and hence lead to a reduction in phytoplankton carbon fixation. Increased desertification in terrestrial ecosystems can lead to increased aeolean loadings of essential micronutrients, such as iron. An increased flux of aeolean micronutrients could fertilize nutrient-replete areas of the open ocean with limiting trace elements, thereby stimulating photosynthetic rates. The factors which limit phytoplankton biomass and photosynthesis are discussed and examined with regard to potential changes in the Earth climate system which can lead the oceans away from steady-state. While it is difficult to confidently deduce changes in either phytoplankton biomass or photosynthetic rates on decadal time scales, time-series analysis of ocean transparency data suggest long-term trends have occurred in the North Pacific Ocean in the 20th century. However, calculations of net carbon uptake by the oceans resulting from phytoplankton photosynthesis suggest that without a supply of nutrients external to the ocean, carbon fixation in the open ocean is not presently a significant sink for excess atmospheric CO2.
海洋浮游植物生物量仅占全球植物碳总量的∽1-2%,但这些生物每年固定的碳量在 300 亿至 500 亿吨之间,约占总量的 40%。在地质时间尺度上,浮游植物光合作用在生物地球化学循环中的重要性有确凿的证据。一般认为,目前浮游植物的生产力处于准稳定状态(在几十年的时间尺度上)。然而,在全球范围内,海洋光合作用过程的稳定性取决于上层海洋的物理循环,因此受大气强烈影响。大气辐射的净通量对于确定上层混合层的深度和营养物质的垂直通量至关重要。后两个参数是决定浮游植物大量繁殖的强度、空间和时间分布的关键。大气辐射预算不是处于稳定状态。在 20 世纪,主要受人为活动的驱动,IR 吸收气体(如 CO2、CH4 和 CFC 以及 NOx)的水平升高可能会导致全球气温升高。大气辐射预算会直接和间接地影响浮游植物的光合作用。大陆和海洋之间的温度差异增大,被认为是海洋边缘风应力增大的原因。风速增加会导致营养物质通量增加。在大多数大洋中心,硝酸盐浓度处于亚微米级,有强有力的证据表明,营养物质胁迫会损害光合作用系统 II 的量子效率。较高的营养物质通量会导致浮游植物生物量增加和更高的生物量特定碳固定率。然而,在海洋环流的中心,辐射加热的增加会减少营养物质向透光带的垂直通量,从而导致浮游植物碳固定的减少。陆地生态系统的沙漠化增加会导致铁等必需微量元素的气载负荷增加。更多的气载微量营养素的输入可以用限制痕量元素来为开阔海域的富营养区施肥,从而刺激光合作用率。本文讨论并检查了限制浮游植物生物量和光合作用的因素,以及可能导致海洋远离稳定状态的地球气候系统的潜在变化。虽然很难有信心推断出浮游植物生物量或光合作用率在几十年的时间尺度上的变化,但对北太平洋海洋透明度数据的时间序列分析表明,20 世纪该地区出现了长期趋势。然而,根据浮游植物光合作用产生的海洋净碳吸收计算,在没有海洋外部供应营养物质的情况下,开阔海洋的碳固定目前并不是大气 CO2 过量的一个重要汇。