Place, date, unit, occasion etc. Slide 1 Eva Walpersdorf, Lisa Heiberg, Charlotte Kjærgaard, Christian B. Koch, David O'Connell, Henning S. Jensen, Hans Christian Bruun Hansen University of Copenhagen, University of Aarhus and University of Southern Denmark Does vivianite (Fe II 3 (PO 4 ) 2 8H 2 O) control phosphate solubility in anoxic soils?
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Does vivianite (Fe II 3(PO4 2 8H2O) control - · PDF fileEPC 0 P i sorption isotherm. Place, date, ... Na + 100 -400 increasing with depth ... •Vivianite control of P i solubility
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Place, date, unit, occasion etc.
Slide 1
Eva Walpersdorf, Lisa Heiberg, Charlotte Kjærgaard, Christian B. Koch, David O'Connell, Henning S. Jensen, Hans Christian Bruun Hansen
University of Copenhagen, University of Aarhus and University of Southern Denmark
Does vivianite (FeII3(PO4)2 8H2O) control
phosphate solubility in anoxic soils?
Place, date, unit, occasion etc.
Slide 2
What is vivianite?
Vivianite as P trap
• Vivianite is an Fe(II)-phosphate (Fe3(PO4)2 8H2O)
• Commonly found in lake sediments, sewage sludges, river sediments
• Forms under non-acid conditions, and at "high" Fe2+ concentrations
• When FeII is oxidized to FeIII vivianite turns blue → metavivianite and santabarbarite
Vivianite
Place, date, unit, occasion etc.
Slide 3
Phosphate retention in anoxic soils
Vivianite as P trap
• Lowland soils potentially accumulates much P
• Retention due to sorption, precipitation, and plant uptake
• P retention is strongly linked to Fe biogeochemistry, and reduction of FeIII oxides may strongly affect retention
Oxic
Anoxic
P in solution (µM)
Sandy meadow soil
Heiberg et al. (2010)
• Distinct increase in Pi
solubility when soil is reduced
• Higher sorption in anoxic soil at high Psol concentrations!
→ Does vivianite precipitate?
EPC0
Pi sorption isotherm
Place, date, unit, occasion etc.
Slide 4
Theory: vivianite solubility and Pi retention
Vivianite as P trap
+ −+ + €2 34
3 2 2
3Fe 2PO 8H2O
Fe (PO4) 8H O
⇒ potential high-affinity Pi
sorption, low EPC0
⇒ points to vivianite as a very important "sorbent" in anoxic soils
Iron phosphate "sponge" structure + underlying iron oxide
Vivianite "sponge" coating (similar morphology seen by Peretyazhko et al., 2010)
Iron oxide
Place, date, unit, occasion etc.
Slide 13
Pore water data- Nov. 2009 - June 2010 -
Vivianite as P trap
Param. Unit Value Comment
pH 6.5 - 6.8
Na+ 100 - 400 increasing with depth
K+ ∼ 50
Mg2+ 25 - 150 incresing with depth
Ca2+ 1200 - 2300 highest in gyttje layer
NH4+ 50 - 350 highest in gyttje layer
Fe2+ µM 500 - 2700 highest in gyttje layer
Mn2+ 30 - 100 constant at 85 µM in gyttje layer
Cl- 400 - 550 very uniform
SO42- 20 - 800 low at top and bottom
HCO3- 2000 - 9000 highest in gyttje layer
PO43- 0.2 - 30 highest in peat layer
Pore water composition from the same depth rather constant for most elements
Place, date, unit, occasion etc.
Slide 14
Pore water composition- pH, FeII and Pi -
Vivianite as P trap
• Constant pH of about 6.8
• Highest FeII
concentrations
• Pi concentrations low
(0.2 - 6 µM), and lower
than for other horizons
FeII (µM)
PO4 (µM)
pH
Gytt
je (
viv
) layer
Place, date, unit, occasion etc.
Slide 15
Pore water: equilibrium with vivianitein the gyttje layer?
Vivianite as P trap
Ksp (viv)
• Near to equilibrium with vivianite late winter; oversaturated during spring
• Not oversaturated with respect to calcium phosphates
oversaturation
undersaturation
IAP =[Fe2+]3[PO43-]2
⇒ pore water data points to equilibrium with vivianite or slight
oversaturation
Place, date, unit, occasion etc.
Slide 16Lab
exp
erim
: R
ele
ase o
f Fe a
nd
Pi
(V
ivia
nit
e d
isso
luti
on
)
Vivianite as P trap
slopesFeII: 251 µM d-1
Pi: 20.6 µM d-1
•FeII concentrations as in the field
•Pi concentrations much higher than in the field
• Highly oversaturated with respect to vivianite; no equili-brium with vivianite
FeII
Pi
Place, date, unit, occasion etc.
Slide 17
Pi sorption isotherms for the gyttje layer- Vivianite precipitation -
Vivianite as P trap
Non-typical isotherm shapes with no sorption maxima as Psol increases→ precipitation
Very high desorption and very high EPC0
Highly oversaturated with respect to vivianite; no equilibrium with vivianite
Vivianite probably precipitates, but no equilibrium with vivianite in lab experiments → slow dissolution/precipitation kinetics
[Fe2+] sol≅ 200 µM
[Fe2+]sol ≅ 500 µM
EPC0
Place, date, unit, occasion etc.
Slide 18
So.... - does vivianite control Pi in reduced soil?
Vivianite as P trap
Field•Vivianite control of Pi solubility during winter times•Oversaturation with respect to vivianite when biological activity increases, more flow, oxidation...
Laboratory•Solution Pi concentrations very high over extended periods•Although vivianite dissolves or precipitates, oversaturation remains high: no fast equilibriation
Does vivianite control Pi solubility?•Systems without perturbation: Yes•Systems with perturbations: NoIn perturbed systems equilibrium takes time to establish - and vivianite-containing soils/sediments rather act as Pi sources
Uncertainty in stoichiometry of the soil vivianite (content of FeIII) ⇒What is the true solubility of the soil vivianite.