Characterizing phosphorus speciation of Chesapeake Bay sediments using chemical extraction, 31P NMR, and X-ray absorption fine structure spectroscopy

Environ Sci Technol. 2015 Jan 6;49(1):203-11. doi: 10.1021/es504648d. Epub 2014 Dec 17.

Abstract

Nutrient contamination has been one of the lingering issues in the Chesapeake Bay because the bay restoration is complicated by temporally and seasonally variable nutrient sources and complex interaction between imported and regenerated nutrients. Differential reactivity of sedimentary phosphorus (P) pools in response to imposed biogeochemical conditions can record past sediment history and therefore a detailed sediment P speciation may provide information on P cycling particularly the stability of a P pool and the formation of one pool at the expense of another. This study examined sediment P speciation from three sites in the Chesapeake Bay: (i) a North site in the upstream bay, (ii) a middle site in the central bay dominated by seasonally hypoxic bottom water, and (iii) a South site at the bay-ocean boundary using a combination of sequential P extraction (SEDEX) and spectroscopic techniques, including (31)P NMR, P X-ray absorption near edge structure spectroscopy (XANES), and Fe extended X-ray absorption fine structure (EXAFS). Results from sequential P extraction reveal that sediment P is composed predominantly of ferric Fe-bound P and authigenic P, which was further confirmed by solid-state (31)P NMR, XANES, and EXAFS analyses. Additionally, solution (31)P NMR results show that the sediments from the middle site contain high amounts of organic P such as monoesters and diesters, compared to the other two sites, but that these compounds rapidly decrease with sediment depth indicating remineralized P could have precipitated as authigenic P. Fe EXAFS enabled to identify the changes in Fe mineral composition and P sinks in response to imposed redox condition in the middle site sediments. The presence of lepidocrocite, vermiculite, and Fe smectite in the middle site sediments indicates that some ferric Fe minerals can still be present along with pyrite and vivianite, and that ferric Fe-bound P pool can be a major P sink in anoxic sediments. These results provide improved insights into sediment P dynamics, particularly the rapid remineralization of organic P and the stability of Fe minerals and the ferric Fe-bound P pool in anoxic sediments in the Chesapeake Bay.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bays
  • Chemical Fractionation / methods
  • Ferric Compounds / analysis
  • Ferric Compounds / chemistry
  • Ferrous Compounds / analysis
  • Ferrous Compounds / chemistry
  • Geologic Sediments / analysis*
  • Geologic Sediments / chemistry
  • Iron / analysis
  • Iron / chemistry
  • Magnetic Resonance Imaging
  • Magnetic Resonance Spectroscopy
  • Mid-Atlantic Region
  • Minerals / chemistry
  • Phosphates / analysis
  • Phosphates / chemistry
  • Phosphorus / analysis*
  • Phosphorus / chemistry
  • Phosphorus Isotopes
  • Silicates / analysis
  • Silicates / chemistry
  • Sulfides / analysis
  • Sulfides / chemistry
  • X-Ray Absorption Spectroscopy / methods

Substances

  • Ferric Compounds
  • Ferrous Compounds
  • Minerals
  • Phosphates
  • Phosphorus Isotopes
  • Silicates
  • Sulfides
  • pyrite
  • ferric oxide
  • Phosphorus
  • Smectite
  • ferrous phosphate
  • Iron