Finnish Environment Institute, Helsinki, Finland.
Ambio. 2009 Sep;38(6):303-8. doi: 10.1579/09-a-656.1.
In marine sediments, the major anaerobic mineralization processes are Fe(III) oxide reduction and sulfate reduction. In this article, we propose that the two alternative microbial mineralization pathways in sediments exert decisively different impacts on aquatic ecosystems. In systems where iron reduction dominates in the recently deposited sediment layers, the fraction of Fe(III) oxides that is dissolved to Fe(II) upon reduction will ultimately be transported to the oxic layer, where it will be reoxidized. Phosphorus, which is released from Fe(III) oxides and decomposing organic matter from the sediment, will be largely trapped by this newly formed Fe(III) oxide layer. Consequently, there are low concentrations of phosphorus in near-bottom and productive water layers and primary production tends to be limited by phosphorus (State 1). By contrast, in systems where sulfate reduction dominates, Fe(III) oxides are reduced by sulfides. This chemical reduction leads to the formation and permanent burial of iron as solid iron sulfides that are unable to capture phosphorus. In addition, the cycling of iron is blocked, and phosphorus is released to overlying water. Owing to the enrichment of phosphorus in water, the nitrogen : phosphorus ratio is lowered and nitrogen tends to limit algal growth, giving an advantage to nitrogen-fixing blue-green algae (State 2). A major factor causing a shift from State 1 to State 2 is an increase in the flux of labile organic carbon to the bottom sediments; upon accelerating eutrophication a critical point will be reached when the availability of Fe(III) oxides in sediments will be exhausted and sulfate reduction will become dominant. Because the reserves of Fe(III) oxides are replenished only slowly, reversal to State 1 may markedly exceed the time needed to reduce the flux of organic carbon to the sediment. A key factor affecting the sensitivity of a coastal system to such a regime shift is formed by the hydrodynamic alterations that decrease the transport of O2 to the near-bottom water, e.g., due to variations in salinity and temperature stratification.
在海洋沉积物中,主要的厌氧矿化过程是三价铁氧化物还原和硫酸盐还原。在本文中,我们提出,沉积物中两种替代的微生物矿化途径对水生生态系统产生决定性的不同影响。在最近沉积的沉积物层中以铁还原为主的系统中,还原时溶解为二价铁的三价铁氧化物的分数最终将被运送到氧化层,在那里它将被再氧化。从三价铁氧化物和沉积物中分解的有机物中释放的磷,将被新形成的三价铁氧化物层大量捕获。因此,在近底和生产力高的水层中磷浓度较低,初级生产力往往受到磷的限制(状态 1)。相比之下,在硫酸盐还原占主导地位的系统中,三价铁氧化物被硫化物还原。这种化学还原导致铁作为不能捕获磷的固体铁硫化物的形成和永久埋藏。此外,铁的循环被阻断,磷被释放到上覆水中。由于水中磷的富集,氮磷比降低,氮往往限制藻类生长,使固氮蓝藻(状态 2)具有优势。从状态 1 向状态 2 转变的一个主要因素是可利用有机碳通量增加到底泥;随着富营养化的加速,当沉积物中三价铁氧化物的可用性耗尽,硫酸盐还原变得占主导地位时,将达到一个临界点。由于三价铁氧化物的储量补充缓慢,向状态 1 的逆转可能明显超过将有机碳通量减少到沉积物所需的时间。影响沿海系统对这种制度转变敏感性的一个关键因素是由氧向近底水的传输减少的水动力改变形成的,例如,由于盐度和温度分层的变化。