Details
| Original language | English |
|---|---|
| Pages (from-to) | 177-188 |
| Number of pages | 12 |
| Journal | Organic geochemistry |
| Volume | 125 |
| Publication status | Published - Nov 2018 |
Abstract
Acquisition of Fe(III) from hardly soluble Fe oxyhydroxides by bacteria, fungi and plants in soil is often facilitated by Fe(III)-chelating siderophores. While the siderophore-promoted dissolution of pure Fe oxyhydroxides and the influence of defined low molecular weight organic acids has been investigated meticulously, studies examining Fe oxyhydroxides coated with more complex adsorbed organic matter (OM) or Fe-OM coprecipitates have been sparse. This study therefore explored the impact of the composition of both adsorbed and coprecipitated OM on the siderophore-promoted dissolution of ferrihydrite (Fh) in relation to (i) surface site coverage and pore blockage, (ii) aggregation state, (iii) charge characteristics and (iv) crystallinity. In addition to pure Fh, Fh-OM adsorption complexes and Fe-OM coprecipitates were synthesized using OM of different origins (extracellular polymeric substances of Bacillus subtilis, natural OM (NOM) extracted from soil Oi and Oa horizons). The Fe-organic associations were characterized by N2 gas adsorption, X-ray photoelectron spectroscopy (XPS), electrophoretic mobility, particle size measurements and desorption experiments. Siderophore-mediated dissolution experiments with desferrioxamine-B (DFOB) were conducted at pH 4 and 7. At pH 4, adsorbed OM provided a more effective protection against DFOB due to its larger sorption affinity. At pH 7, the surface site blockage by adsorbed OM at comparable C loadings was less effective, while less aggregated particles were more prone to dissolution. For OM coprecipitated with Fe, there was no distinct accelerating or inhibiting effect on DFOB-promoted dissolution to be found. Initial Fe dissolution rates at given soil conditions were thus affected by both the type of OM and the sorption procedure. Our results therefore corroborate the importance of considering the heterogeneous composition of soil OM when investigating the mobilization of Fe-organic associations.
Keywords
- Coprecipitation, Desferrioxamine-B, Extracellular polymeric substances, Ferrihydrite, Mineral-organic associations, Natural organic matter, Siderophores
ASJC Scopus subject areas
- Earth and Planetary Sciences(all)
- Geochemistry and Petrology
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In: Organic geochemistry, Vol. 125, 11.2018, p. 177-188.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Siderophore-promoted dissolution of ferrihydrite associated with adsorbed and coprecipitated natural organic matter
AU - Poggenburg, Christine
AU - Mikutta, Robert
AU - Liebmann, Patrick
AU - Koch, Markus
AU - Guggenberger, Georg
N1 - Funding information: This study was financially supported by the NTH-Graduate School “Geofluxes” of the Federal State of Lower Saxony . We are grateful to Axel Schippers for his assistance with the preparation of the EPS. Furthermore, we would like to thank two anonymous reviewers for their very helpful comments. Appendix A
PY - 2018/11
Y1 - 2018/11
N2 - Acquisition of Fe(III) from hardly soluble Fe oxyhydroxides by bacteria, fungi and plants in soil is often facilitated by Fe(III)-chelating siderophores. While the siderophore-promoted dissolution of pure Fe oxyhydroxides and the influence of defined low molecular weight organic acids has been investigated meticulously, studies examining Fe oxyhydroxides coated with more complex adsorbed organic matter (OM) or Fe-OM coprecipitates have been sparse. This study therefore explored the impact of the composition of both adsorbed and coprecipitated OM on the siderophore-promoted dissolution of ferrihydrite (Fh) in relation to (i) surface site coverage and pore blockage, (ii) aggregation state, (iii) charge characteristics and (iv) crystallinity. In addition to pure Fh, Fh-OM adsorption complexes and Fe-OM coprecipitates were synthesized using OM of different origins (extracellular polymeric substances of Bacillus subtilis, natural OM (NOM) extracted from soil Oi and Oa horizons). The Fe-organic associations were characterized by N2 gas adsorption, X-ray photoelectron spectroscopy (XPS), electrophoretic mobility, particle size measurements and desorption experiments. Siderophore-mediated dissolution experiments with desferrioxamine-B (DFOB) were conducted at pH 4 and 7. At pH 4, adsorbed OM provided a more effective protection against DFOB due to its larger sorption affinity. At pH 7, the surface site blockage by adsorbed OM at comparable C loadings was less effective, while less aggregated particles were more prone to dissolution. For OM coprecipitated with Fe, there was no distinct accelerating or inhibiting effect on DFOB-promoted dissolution to be found. Initial Fe dissolution rates at given soil conditions were thus affected by both the type of OM and the sorption procedure. Our results therefore corroborate the importance of considering the heterogeneous composition of soil OM when investigating the mobilization of Fe-organic associations.
AB - Acquisition of Fe(III) from hardly soluble Fe oxyhydroxides by bacteria, fungi and plants in soil is often facilitated by Fe(III)-chelating siderophores. While the siderophore-promoted dissolution of pure Fe oxyhydroxides and the influence of defined low molecular weight organic acids has been investigated meticulously, studies examining Fe oxyhydroxides coated with more complex adsorbed organic matter (OM) or Fe-OM coprecipitates have been sparse. This study therefore explored the impact of the composition of both adsorbed and coprecipitated OM on the siderophore-promoted dissolution of ferrihydrite (Fh) in relation to (i) surface site coverage and pore blockage, (ii) aggregation state, (iii) charge characteristics and (iv) crystallinity. In addition to pure Fh, Fh-OM adsorption complexes and Fe-OM coprecipitates were synthesized using OM of different origins (extracellular polymeric substances of Bacillus subtilis, natural OM (NOM) extracted from soil Oi and Oa horizons). The Fe-organic associations were characterized by N2 gas adsorption, X-ray photoelectron spectroscopy (XPS), electrophoretic mobility, particle size measurements and desorption experiments. Siderophore-mediated dissolution experiments with desferrioxamine-B (DFOB) were conducted at pH 4 and 7. At pH 4, adsorbed OM provided a more effective protection against DFOB due to its larger sorption affinity. At pH 7, the surface site blockage by adsorbed OM at comparable C loadings was less effective, while less aggregated particles were more prone to dissolution. For OM coprecipitated with Fe, there was no distinct accelerating or inhibiting effect on DFOB-promoted dissolution to be found. Initial Fe dissolution rates at given soil conditions were thus affected by both the type of OM and the sorption procedure. Our results therefore corroborate the importance of considering the heterogeneous composition of soil OM when investigating the mobilization of Fe-organic associations.
KW - Coprecipitation
KW - Desferrioxamine-B
KW - Extracellular polymeric substances
KW - Ferrihydrite
KW - Mineral-organic associations
KW - Natural organic matter
KW - Siderophores
UR - http://www.scopus.com/inward/record.url?scp=85054192444&partnerID=8YFLogxK
U2 - 10.1016/j.orggeochem.2018.09.004
DO - 10.1016/j.orggeochem.2018.09.004
M3 - Article
AN - SCOPUS:85054192444
VL - 125
SP - 177
EP - 188
JO - Organic geochemistry
JF - Organic geochemistry
SN - 0146-6380
ER -