TY - JOUR
T1 - Influence of natural organic matter on the bioavailability and preservation of organic phosphorus in lake sediments
AU - Zhu, Yuanrong
AU - Wu, Fengchang
AU - He, Zhongqi
AU - Giesy, John P.
AU - Feng, Weiying
AU - Mu, Yunsong
AU - Feng, Chenglian
AU - Zhao, Xiaoli
AU - Liao, Haiqing
AU - Tang, Zhi
PY - 2015/3/18
Y1 - 2015/3/18
N2 - Information about the bioavailability and sequestration of organic phosphorus (Po) in sediments is fundamental to understanding biogeochemical cycling of phosphorus (P) in eutrophic lakes. However, the processes governing preservation of Po in sediments are still poorly understood. Sequential extraction of P-o by H2O (H2O-P-o) and NaOH-EDTA (NaOH-EDTA P-o), in combination with enzymatic hydrolysis/P-31 NMR, was applied to estimate the bioavailability of Po in sediments of Lake Tai (Ch: Taihu), China. Of H2O-P-o and NaOH-EDTA P-o, 45.5-89.4% and 30.4-71.3% respectively were hydrolyzed by phosphatase, and therefore considered to be biologically available. Of NaOH-EDTA Po, 28.7-69.6% could not be hydrolyzed by phosphatase; this portion was characterized by P-31 NMR as monoester P and/or diester P. Simulation experiments of hydrolysis of model P-o compounds in the presence of humic acids (HA), which were used as a model for natural organic matter (NOM), and metals, including Al, Ca, and Fe, have demonstrated that enzymatic hydrolysis of labile monoester P was weakly reduced by HA or metal ions. Condensed phosphate (e.g., pyrophosphate) and phytate-like P (e.g., inositol phosphates) were resistant to enzymatic hydrolysis in the presence of HA and/or metal ions, which indicated that they may be possibly preserved in sediments. These observations suggest that NOM in sediments can be a significant factor determining the bioavailability and preservation of P-o in sediments. The presence of metals would enhance the effect of NOM on preservation of P-o in sediments. Formation of P-o-metal-HA or P-o-metal complexes might be mechanisms responsible for these processes. (C) 2015 Elsevier B.V. All rights reserved.
AB - Information about the bioavailability and sequestration of organic phosphorus (Po) in sediments is fundamental to understanding biogeochemical cycling of phosphorus (P) in eutrophic lakes. However, the processes governing preservation of Po in sediments are still poorly understood. Sequential extraction of P-o by H2O (H2O-P-o) and NaOH-EDTA (NaOH-EDTA P-o), in combination with enzymatic hydrolysis/P-31 NMR, was applied to estimate the bioavailability of Po in sediments of Lake Tai (Ch: Taihu), China. Of H2O-P-o and NaOH-EDTA P-o, 45.5-89.4% and 30.4-71.3% respectively were hydrolyzed by phosphatase, and therefore considered to be biologically available. Of NaOH-EDTA Po, 28.7-69.6% could not be hydrolyzed by phosphatase; this portion was characterized by P-31 NMR as monoester P and/or diester P. Simulation experiments of hydrolysis of model P-o compounds in the presence of humic acids (HA), which were used as a model for natural organic matter (NOM), and metals, including Al, Ca, and Fe, have demonstrated that enzymatic hydrolysis of labile monoester P was weakly reduced by HA or metal ions. Condensed phosphate (e.g., pyrophosphate) and phytate-like P (e.g., inositol phosphates) were resistant to enzymatic hydrolysis in the presence of HA and/or metal ions, which indicated that they may be possibly preserved in sediments. These observations suggest that NOM in sediments can be a significant factor determining the bioavailability and preservation of P-o in sediments. The presence of metals would enhance the effect of NOM on preservation of P-o in sediments. Formation of P-o-metal-HA or P-o-metal complexes might be mechanisms responsible for these processes. (C) 2015 Elsevier B.V. All rights reserved.
KW - Enzymatic hydrolysis
KW - P-31 NMR
KW - Organic phosphorus
KW - Bioavailability
KW - Preservation
KW - Natural organic matter
U2 - 10.1016/j.chemgeo.2015.01.006
DO - 10.1016/j.chemgeo.2015.01.006
M3 - RGC 21 - Publication in refereed journal
SN - 0009-2541
VL - 397
SP - 51
EP - 60
JO - Chemical Geology
JF - Chemical Geology
ER -