Oxygen Controls the Phosphorus Release from Lake Sediments – a Long‐Lasting Paradigm in Limnology

缺氧水域 低角膜缘 有机质 沉积物 环境化学 氧气 溶解 氧化还原 矿化(土壤科学) 化学 营养物 生态学 环境科学 地质学 土壤科学 土壤水分 生物 无机化学 富营养化 物理化学 古生物学 有机化学
作者
Michael Hupfer,Jörg Lewandowski
出处
期刊:International Review of Hydrobiology [Wiley]
卷期号:93 (4-5): 415-432 被引量:515
标识
DOI:10.1002/iroh.200711054
摘要

Abstract The pioneer works of Einsele, Mortimer, and Ohle on the linking between phosphorus (P) and iron (Fe) cycles seven decades ago created the theoretical basis for a long‐standing paradigm among limnologists i.e. , ‘oxygen controls the P release from sediments’. While many empirical studies as well as strong correlations between oxygen depletion and P release seem to support this paradigm, various field observations, laboratory experiments, and repeated failures of hypolimnetic oxygenation measures cast doubt on its universal validity. The temporal existence of a thin oxidized sediment surface‐layer could affect only fluctuations of the temporary P pool at the sediment surface but not the long‐term P retention. On longer time scales P release is the imbalance between P sedimentation and P binding capacity of anoxic sediment layers. The P retention of lake sediments strongly depends on sediment characteristics and land use of the catchment. The presence of redox‐insensitive P‐binding systems such as Al(OH) 3 and unreducible Fe(III) minerals can enhance the P retention and completely prevent P release even in case of anoxic conditions. Alternative release mechanisms such as a dissolution of calcium‐bound P and decomposition of organic P under both, aerobic and anaerobic conditions, are often more important than the redox driven Fe‐coupled P cycle. Additionally, bacteria affect P cycling not only by altering the redox conditions but also by releasing P during mineralization of organic matter and by accumulation and release of bacterial P. Since microbial processes consume oxygen and liberate P it is difficult to distinguish whether oxygen depletion is the result or the cause of P release. Nowadays, the old paradigm is discarded and a paradigm shift takes place. Sedimentary P exchange ought to be considered as a complex process which is mainly determined by the amount and species of settled P as well as their subsequent diagenetic transformation in the sediment. The classical paradigm is only valid in special cases since reality is much more complex than suggested by that paradigm. Everything should be made simple as possible, but not simpler! Albert Einstein (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
思源应助安详苠采纳,获得30
刚刚
刚刚
刚刚
李爱国应助wxs采纳,获得10
2秒前
默默的发布了新的文献求助10
3秒前
3秒前
蓝白榆发布了新的文献求助10
3秒前
贝塔发布了新的文献求助10
4秒前
没有肥肉的二师兄完成签到 ,获得积分10
4秒前
上官若男应助小小同学采纳,获得10
4秒前
JamesPei应助li锂狸采纳,获得10
5秒前
水告完成签到,获得积分10
5秒前
Sea_U应助田小冉采纳,获得10
5秒前
hu发布了新的文献求助10
6秒前
cyy发布了新的文献求助10
6秒前
Azhar完成签到,获得积分10
6秒前
6秒前
Akim应助丰富无色采纳,获得30
6秒前
禹宛白发布了新的文献求助10
7秒前
像棉花糖的云完成签到,获得积分10
9秒前
yx阿聪完成签到,获得积分10
9秒前
9秒前
土豆泥加火鸡面完成签到,获得积分10
9秒前
9秒前
123567完成签到 ,获得积分10
9秒前
molihuakai应助宝宝贝贝采纳,获得10
9秒前
9秒前
打打应助5_羟色胺采纳,获得10
9秒前
洛书完成签到,获得积分10
10秒前
anzer发布了新的文献求助10
11秒前
alu发布了新的文献求助10
11秒前
12秒前
12秒前
鹿初蓝完成签到,获得积分10
12秒前
WL发布了新的文献求助10
12秒前
13秒前
13秒前
可爱的函函应助Dylan采纳,获得10
13秒前
scott910806完成签到,获得积分10
13秒前
xh999完成签到,获得积分10
14秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Green Fire Retardants for Polymeric Materials 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7615494
求助须知:如何正确求助?哪些是违规求助? 9190800
关于积分的说明 19693491
捐赠科研通 7188075
什么是DOI,文献DOI怎么找? 3271364
关于科研通互助平台的介绍 2434568
邀请新用户注册赠送积分活动 2266438