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Title: Phosphorus Speciation in Atmospherically Deposited Particulate Matter and Implications for Terrestrial Ecosystem Productivity

Technical Report ·
DOI:https://doi.org/10.2172/1570288· OSTI ID:1570288
ORCiD logo [1];  [1];  [1];  [1];  [1];  [2];  [3]
  1. Univ. of California, Merced, CA (United States)
  2. Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
  3. Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Rocky Mountain Biological Lab., Gothic, CO (United States)

Chemical forms of P in airborne particulate matter (PM) are poorly known and do not correlate with solubility or extraction measurements commonly used to infer speciation. We used P X-ray absorption near-edge structure (XANES) and 31-P nuclear magnetic resonance (NMR) to determine P species in PM collected at four mountain sites (Colorado and California, USA). Organic P species dominated samples from high elevations, with organic P estimated at 65–100% of total P in bulk samples by XANES and 79–88% in extracted fractions (62–84% of total P) by NMR regardless of particle size (≥ 10 µm or 1–10 µm). Phosphorus monoester and diester organic species were dominant and present in about equal proportions, with low fractions of inorganic P species. By comparison, PM from low elevation contained mixtures of organic and inorganic P, with organic P estimated at 30-60% of total P. Intercontinental PM transport determined from radiogenic lead (Pb) isotopes varied from 0-59% (mean 37%) Asian-sourced Pb at high elevation, whereas stronger regional PM inputs were found at low elevation. Airborne flux of bioavailable P to high elevation ecosystems may be twice as high as estimated by global models, which will disproportionately affect net primary productivity.

Research Organization:
Univ. of California, Merced, CA (United States)
Sponsoring Organization:
Office of Science (SC), Biological and Environmental Research (BER). Earth and Environmental Systems Science Division
Contributing Organization:
Stanford Synchrotron Radiation Lightsource, operated by Stanford University on behalf of the U.S. Department of Energy; Canadian Light Source, Saskatchewan, CA
DOE Contract Number:
SC0016479
OSTI ID:
1570288
Report Number(s):
DOE-UCMerced-SC0016479
Country of Publication:
United States
Language:
English