Welcome to the NOAA Institutional Repository |
Stacks Logo
Advanced Search
Select up to three search categories and corresponding keywords using the fields to the right. Refer to the Help section for more detailed instructions.
 
 
Help
Clear All Simple Search
Advanced Search
Constraining N2O emissions since 1940 using firn air isotope measurements in both hemispheres
  • Published Date:
    2017
  • Source:
    Atmospheric Chemistry and Physics, 17(7), 4539-4564.
Filetype[PDF-8.06 MB]


This document cannot be previewed automatically as it exceeds 5 MB
Please click the thumbnail image to view the document.
Constraining N2O emissions since 1940 using firn air isotope measurements in both hemispheres
Details:
  • Description:
    N2O is currently the third most important anthropogenic greenhouse gas in terms of radiative forcing and its atmospheric mole fraction is rising steadily. To quantify the growth rate and its causes over the past decades, we performed a multi-site reconstruction of the atmospheric N2O mole fraction and isotopic composition using new and previously published firn air data collected from Greenland and Antarctica in combination with a firn diffusion and densification model. The multi-site reconstruction showed that while the global mean N2O mole fraction increased from (290 +/- 1) nmol mol(-1) in 1940 to (322 +/- 1) nmol mol(-1) in 2008, the isotopic composition of atmospheric N2O decreased by (-2.2 +/- 0.2)parts per thousand for delta N-15(av), (-1.0 +/- 0.3)parts per thousand for delta O-18, (-1.3 +/- 0.6)parts per thousand for delta N-15(alpha), and (-2.8 +/- 0.6)parts per thousand for delta N-15(beta) over the same period. The detailed temporal evolution of the mole fraction and isotopic composition derived from the firn air model was then used in a two-box atmospheric model (comprising a stratospheric box and a tropospheric box) to infer changes in the isotopic source signature over time. The precise value of the source strength depends on the choice of the N2O lifetime, which we choose to fix at 123 years. The average isotopic composition over the investigated period is delta N-15(av) = (-7.6 +/- 0.8)parts per thousand (vs. air-N-2), delta O-18 D (32.2 +/- 0.2)parts per thousand (vs. Vienna Standard Mean Ocean Water - VSMOW) for delta O-18, delta N-15(alpha) = (-3.0 +/- 1.9)parts per thousand and delta N-15(beta) = (-11.7 +/- 2.3) parts per thousand. delta N-15(av), and delta N-15(beta) show some temporal variability, while for the other signatures the error bars of the reconstruction are too large to retrieve reliable temporal changes. Possible processes that may explain trends in N-15 are discussed. The N-15 site preference (= delta N-15 alpha - delta N-15(beta)) provides evidence of a shift in emissions from denitrification to nitrification, although the uncertainty envelopes are large.
  • Document Type:
  • Main Document Checksum:
  • Supporting Files:
    No Additional Files
You May Also Like: