溶解性多聚磷酸盐(poly-P)在太湖竺山湾湖区泥-水界面的降解和影响因素初探
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1.中国科学院南京地理与湖泊研究所,湖泊与流域水安全全国重点实验室,南京 211135 ;2.中国科学院大学,北京 100049 ;3.南京师范大学环境学院,南京 210023

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国家自然科学基金项目(42177227);江苏省社会发展项目(BE2022858);地方项目(HLZC2024009)联合资助


Soluble polyphosphate (poly-P) degradation and its influencing factors at the sediment-water interface in Zhushan Bay, Lake Taihu
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1.State Key Laboratory of Lake and Watershed Science for Water Security, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences, Nanjing 211135 , P.R.China ;2.University of Chinese Academy of Sciences, Beijing 100049 , P.R.China ;3.School of Environment, Nanjing Normal University, Nanjing 210023 , P.R.China

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    摘要:

    多聚磷酸盐(poly-P,简称聚磷)作为一种生物体普遍存在且生物活性高的磷组分,在富营养化水体的磷生物地球化学循环中至关重要。为探明聚磷在湖体沉积物-水界面和水体降解转化过程及其与湖底关键环境因子的响应过程,采集太湖竺山湾水域原位样品,模拟近自然条件下聚磷在湖体中的降解与转化过程。结果表明,在近自然条件下,溶解性聚磷的短期水解没有受到明显限制,随浓度提高水解作用增强,2 d后高浓度聚磷水解产生的溶解性活性磷(SRP)浓度增长速率可达到(0.1±0.01)mg/(L·d)。聚磷的水解以生物降解为主,影响其降解速率的主要因素包括溶解氧、碳源、温度以及水动力扰动导致的底泥再悬浮过程,低溶解氧浓度能够加速聚磷的水解进程,并使得SRP浓度提前12 h达到峰值;碳源的添加能够略提高聚磷的水解速率,并能够在培养周期内持续促进SRP的释放,净增长量达到对照组的2倍;低温能够显著降低聚磷的水解速率,但整体SRP浓度仍然处于升高状态;扰动导致的底泥再悬浮能够提高聚磷的水解速率以及SRP浓度峰值。聚磷在沉积物中主要以强结合态存在于Al-P组分中并不断释放和进一步水解,仅微量以游离态赋存于沉积物和间隙水。溶解性聚磷在近自然条件下能够在48 h内迅速沉降水解,并对水体SRP升高持续贡献。本研究探讨了水体中聚磷酸盐的赋存特性及其快速水解周转,为阐明夏秋季湖泊藻细胞指数增殖期的活性磷供给源以及多聚磷在磷循环中的生物地球化学作用提供了理论依据。

    Abstract:

    Polyphosphate (poly-P), a phosphorus component that is widely present in organisms and exhibits high biological activity, plays a critical role in the phosphorus biogeochemical cycling in eutrophic water bodies. To elucidate the degradation and transformation processes of poly-P at the sediment-water interface and within the water column, as well as its response to key environmental factors in lake sediments, in situ samples were collected from the Zhushan Bay area of Lake Taihu. These samples were used to simulate near-natural conditions for studying the degradation and transformation of poly-P. The results indicated that under near-natural conditions, the short-term hydrolysis rate of dissolved poly-P showed no obvious upper limit and increased with rising concentrations. After two days, the soluble reactive phosphorus (SRP) concentration generated by the hydrolysis of high-concentration poly-P could reach (0.1±0.01) mg/(L·d). The hydrolysis of poly-P was primarily driven by biological degradation, with key factors influencing the degradation rate including dissolved oxygen (DO), carbon sources, temperature, and sediment resuspension caused by disturbances. Low DO accelerated the hydrolysis of poly-P and brought the SRP to its peak 12 hours earlier. The addition of carbon sources slightly increased the hydrolysis rate and promoted sustained SRP release throughout the incubation period, with a net increase reaching twice that of the control group. Low temperatures significantly reduced the hydrolysis rate, although the overall SRP continued to rise. Disturbances that led to sediment resuspension increased both the hydrolysis rate of poly-P and the peak of SRP. In the sediment, poly-P mainly existed in a strongly bound form within the Al-P fraction, undergoing continuous release and further hydrolysis, while only trace amounts were present as free poly-P in the sediment and pore water. Dissolved poly-P could rapidly settle and hydrolyze within 48 hours under near-natural conditions, contributing to the sustained supply of SRP to the water column. This study on the occurrence and rapid hydrolytic turnover of poly-P in the water column provides insights into tracing and clarifying the sources of active phosphorus that fuel algal cell proliferation during the summer and autumn seasons. It also sheds light on the biogeochemical processes involving polyphosphate in the phosphorus cycle of water bodies.

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张云帆,蔡健霞,童丞飞,周梓怡,郑尚杰,郭柳佳,古小治.溶解性多聚磷酸盐(poly-P)在太湖竺山湾湖区泥-水界面的降解和影响因素初探.湖泊科学,2025,37(5):1537-1547. Zhang Yunfan, Cai Jianxia, Tong Chengfei, Zhou Ziyi, Zheng Shangjie, Guo Liujia, Gu Xiaozhi. Soluble polyphosphate (poly-P) degradation and its influencing factors at the sediment-water interface in Zhushan Bay, Lake Taihu. Journal of Lake Sciences,2025,37(5):1537-1547. DOI:10.18307/2025.0514

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  • 收稿日期:2024-10-14
  • 最后修改日期:2024-12-10
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  • 在线发布日期: 2025-09-07
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