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海洋环境中铁的有机络合作用:综述

The organic complexation of iron in the marine environment: a review.

作者信息

Gledhill Martha, Buck Kristen N

机构信息

Ocean and Earth Science, National Oceanography Centre - Southampton, University of Southampton Southampton, UK.

出版信息

Front Microbiol. 2012 Feb 28;3:69. doi: 10.3389/fmicb.2012.00069. eCollection 2012.

Abstract

Iron (Fe) is an essential micronutrient for marine organisms, and it is now well established that low Fe availability controls phytoplankton productivity, community structure, and ecosystem functioning in vast regions of the global ocean. The biogeochemical cycle of Fe involves complex interactions between lithogenic inputs (atmospheric, continental, or hydrothermal), dissolution, precipitation, scavenging, biological uptake, remineralization, and sedimentation processes. Each of these aspects of Fe biogeochemical cycling is likely influenced by organic Fe-binding ligands, which complex more than 99% of dissolved Fe. In this review we consider recent advances in our knowledge of Fe complexation in the marine environment and their implications for the biogeochemistry of Fe in the ocean. We also highlight the importance of constraining the dissolved Fe concentration value used in interpreting voltammetric titration data for the determination of Fe speciation. Within the published Fe speciation data, there appear to be important temporal and spatial variations in Fe-binding ligand concentrations and their conditional stability constants in the marine environment. Excess ligand concentrations, particularly in the truly soluble size fraction, seem to be consistently higher in the upper water column, and especially in Fe-limited, but productive, waters. Evidence is accumulating for an association of Fe with both small, well-defined ligands, such as siderophores, as well as with larger, macromolecular complexes like humic substances, exopolymeric substances, and transparent exopolymers. The diverse size spectrum and chemical nature of Fe ligand complexes corresponds to a change in kinetic inertness which will have a consequent impact on biological availability. However, much work is still to be done in coupling voltammetry, mass spectrometry techniques, and process studies to better characterize the nature and cycling of Fe-binding ligands in the marine environment.

摘要

铁(Fe)是海洋生物必需的微量营养素,目前已经明确,全球海洋广大区域中,铁的可利用性低会控制浮游植物的生产力、群落结构以及生态系统功能。铁的生物地球化学循环涉及岩石成因输入(大气、大陆或热液)、溶解、沉淀、清除、生物摄取、再矿化和沉积过程之间的复杂相互作用。铁生物地球化学循环的每个方面都可能受到有机铁结合配体的影响,这些配体络合了超过99%的溶解态铁。在这篇综述中,我们考虑了我们对海洋环境中铁络合作用的认识的最新进展及其对海洋中铁生物地球化学的影响。我们还强调了限制用于解释伏安滴定数据以确定铁形态的溶解态铁浓度值的重要性。在已发表的铁形态数据中,海洋环境中铁结合配体浓度及其条件稳定常数似乎存在重要的时间和空间变化。过量的配体浓度,特别是在真正可溶的粒径部分,似乎在上层水柱中一直较高,尤其是在铁限制但生产力高的水域。越来越多的证据表明,铁与小的、定义明确的配体(如铁载体)以及与腐殖质、胞外聚合物和透明胞外聚合物等较大的大分子络合物有关。铁配体络合物的不同粒径谱和化学性质对应于动力学惰性的变化,这将对生物可利用性产生相应影响。然而,在将伏安法、质谱技术和过程研究相结合以更好地表征海洋环境中铁结合配体的性质和循环方面,仍有许多工作要做。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb4/3289268/1f5960e7c2f5/fmicb-03-00069-g001.jpg

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