scholarly journals Sediment phosphorus speciation and mobility under dynamic redox conditions

2017 ◽  
Vol 14 (14) ◽  
pp. 3585-3602 ◽  
Author(s):  
Chris T. Parsons ◽  
Fereidoun Rezanezhad ◽  
David W. O'Connell ◽  
Philippe Van Cappellen

Abstract. Anthropogenic nutrient enrichment has caused phosphorus (P) accumulation in many freshwater sediments, raising concerns that internal loading from legacy P may delay the recovery of aquatic ecosystems suffering from eutrophication. Benthic recycling of P strongly depends on the redox regime within surficial sediment. In many shallow environments, redox conditions tend to be highly dynamic as a result of, among others, bioturbation by macrofauna, root activity, sediment resuspension and seasonal variations in bottom-water oxygen (O2) concentrations. To gain insight into the mobility and biogeochemistry of P under fluctuating redox conditions, a suspension of sediment from a hypereutrophic freshwater marsh was exposed to alternating 7-day periods of purging with air and nitrogen gas (N2), for a total duration of 74 days, in a bioreactor system. We present comprehensive data time series of bulk aqueous- and solid-phase chemistry, solid-phase phosphorus speciation and hydrolytic enzyme activities demonstrating the mass balanced redistribution of P in sediment during redox cycling. Aqueous phosphate concentrations remained low ( ∼  2.5 µM) under oxic conditions due to sorption to iron(III) oxyhydroxides. During anoxic periods, once nitrate was depleted, the reductive dissolution of iron(III) oxyhydroxides released P. However, only 4.5 % of the released P accumulated in solution while the rest was redistributed between the MgCl2 and NaHCO3 extractable fractions of the solid phase. Thus, under the short redox fluctuations imposed in the experiments, P remobilization to the aqueous phase remained relatively limited. Orthophosphate predominated at all times during the experiment in both the solid and aqueous phase. Combined P monoesters and diesters accounted for between 9 and 16 % of sediment particulate P. Phosphatase activities up to 2.4 mmol h−1 kg−1 indicated the potential for rapid mineralization of organic P (Po), in particular during periods of aeration when the activity of phosphomonoesterases was 37 % higher than under N2 sparging. The results emphasize that the magnitude and timing of internal P loading during periods of anoxia are dependent on both P redistribution within sediments and bottom-water nitrate concentrations.

2017 ◽  
Author(s):  
Chris T. Parsons ◽  
Fereidoun Rezanezhad ◽  
David W. O'Connell ◽  
Philippe Van Cappellen

Abstract. Anthropogenic nutrient enrichment has caused phosphorus (P) accumulation in many freshwater sediments, raising concerns that internal loading from legacy P may delay the recovery of aquatic ecosystems suffering from eutrophication. Benthic recycling of P strongly depends on the redox regime at the sediment-water interface (SWI) that, in many shallow environments, tends to be highly dynamic as a result of, among others, bioturbation by macrofauna, root activity, sediment resuspension and seasonal variations in bottom water oxygen (O2) concentrations. To gain insight into the mobility and biogeochemistry of P under fluctuating redox conditions, a suspension of sediment from a hyper-eutrophic freshwater marsh was exposed to alternating 7-day periods of purging with air and nitrogen gas (N2), for a total duration of 74 days. At the start of each anoxic period, algal necromass was added to simulate the deposition of fresh autochtonous organic matter. Phosphatase activities up to 2.4 mmol h−1 kg−1 indicated the potential for rapid mineralization of added organic-P (Po), in particular during the periods of aeration when the activity of phosphomonoesterases was up to 37 % higher than under N2 sparging. Aqueous phosphate concentrations remained low (~2.5 µM) under oxic conditions, due to sorption to Fe/Mn-oxides. During anoxic periods, once nitrate was depleted, the reductive dissolution of Fe/Mn-oxides released P. However, only 4.5 % of the released P accumulated in solution while the rest was redistributed among the particulate phases, including the humic fraction. Thus, under the relatively short-term redox fluctuations imposed in the experiments, P remobilization to the aqueous phase remained relatively limited and poly-phosphate did not accumulate. The results also emphasize the important control bottom water nitrate concentrations may exert on internal P loading in eutrophic environments.


1982 ◽  
Vol 14 (12) ◽  
pp. 107-125 ◽  
Author(s):  
Roland Wollast

A comparison of the concentration of dissolved and of particulate heavy metals in the aquatic system indicates that these elements are strongly enriched in the suspended matter. The transfer between the aqueous phase and the solid phase may be due to dissolution-precipitation reactions, adsorption-desorption processes or biological processes. When these processes are identified, it is further possible to develop mathematical models which describe the behaviour of these elements. The enrichment of heavy metals in the particulate phase suspended or deposited and in aquatic organisms constitutes a powerful tool in order to evaluate sources of pollution.


2001 ◽  
Vol 32 ◽  
pp. 269-270
Author(s):  
J.E. WILLIAMS ◽  
F.J. DENTENER ◽  
A.R. van den BERG

2018 ◽  
Vol 46 (14) ◽  
pp. 6996-7005 ◽  
Author(s):  
Erin E Duffy ◽  
Daniele Canzio ◽  
Tom Maniatis ◽  
Matthew D Simon

2018 ◽  
Vol 20 (16) ◽  
pp. 10960-10977 ◽  
Author(s):  
Erik H. Hoffmann ◽  
Andreas Tilgner ◽  
Ralf Wolke ◽  
Olaf Böge ◽  
Arno Walter ◽  
...  

An aqueous-phase chemistry mechanism for the oxidation of aromatic compounds in the atmosphere is developed based on available kinetic data. Detailed model studies successfully describe the oxidation and functionalization of monoaromatic compounds in the atmosphere.


1997 ◽  
Vol 435 (1-2) ◽  
pp. 189-203 ◽  
Author(s):  
M.S. Passos ◽  
M.A. Queiros ◽  
T. Le Gall ◽  
S.K. Ibrahim ◽  
C.J. Pickett

2013 ◽  
Vol 13 (3) ◽  
pp. 1177-1192 ◽  
Author(s):  
C. Knote ◽  
D. Brunner

Abstract. Clouds are reaction chambers for atmospheric trace gases and aerosols, and the associated precipitation is a major sink for atmospheric constituents. The regional chemistry-climate model COSMO-ART has been lacking a description of wet scavenging of gases and aqueous-phase chemistry. In this work we present a coupling of COSMO-ART with a wet scavenging and aqueous-phase chemistry scheme. The coupling is made consistent with the cloud microphysics scheme of the underlying meteorological model COSMO. While the choice of the aqueous-chemistry mechanism is flexible, the effects of a simple sulfur oxidation scheme are shown in the application of the coupled system in this work. We give details explaining the coupling and extensions made, then present results from idealized flow-over-hill experiments in a 2-D model setup and finally results from a full 3-D simulation. Comparison against measurement data shows that the scheme efficiently reduces SO2 trace gas concentrations by 0.3 ppbv (−30%) on average, while leaving O3 and NOx unchanged. PM10 aerosol mass was increased by 10% on average. While total PM2.5 changes only little, chemical composition is improved notably. Overestimations of nitrate aerosols are reduced by typically 0.5–1 μg m−3 (up to −2 μg m−3 in the Po Valley) while sulfate mass is increased by 1–1.5 μg m−3 on average (up to 2.5 μg m−3 in Eastern Europe). The effect of cloud processing of aerosols on its size distribution, i.e. a shift towards larger diameters, is observed. Compared against wet deposition measurements the system tends to underestimate the total wet deposited mass for the simulated case study.


2000 ◽  
Vol 41 (30) ◽  
pp. 5617-5622 ◽  
Author(s):  
Concepción Alonso ◽  
Michael H Nantz ◽  
Mark J Kurth

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