As described in Kaiser et al. (2007), isotopic data is corrected and standardized to international reference materials IAEA-N3, USGS34, and USGS35, which are run 3-9 times with each sample run. For d15N, samples are corrected for isobaric interferences and a blank associated with the bacteria. For d18O, samples are corrected for isobaric interferences, blank, and exchange between sample nitrate and background water that takes place during denitrification to nitrous oxide. The pooled standard deviation for the reference materials are (n=88): 0.2 per mil for d15N and 0.7 per mil for d18O of IAEA-N3; 0.3 per mil for d15N and 0.7 per mil for d18O of USGS34; and 0.7 per mil for d18O of USGS35 (sample d15N is not corrected for d15N of USGS35, this is used as an internal quality check and pooled standard deviation across all runs in 0.2 per mil). 10 samples were run in duplicate or triplicate and the paired pooled standard deviation (n=10) is 0.2 per mil for d15N and 0.4 per mil for d18O. Pooled standard deviation for USGS34 and USGS35 run for D17O is 0.6 and 0.9 per mil each (n=14 and 15, respectively), and replicate samples were 0.9 per mil (n=4).
Oxygen and hydrogen isotope ratios of water (d18O-H2O vs. VSMOW, dD-H2O vs. VSMOW) were measured using wavelength-scanned cavity-down ring spectroscopy on a Picarro L1102-I liquid analyzer calibrated to international reference standards USGS46, USGS49 and VSMOW. Raw data are corrected for memory and drift effects followed by normalization using a standard calibration (Vaughn and Claymoore, INSTAAR, University of Colorado). Precision for d18O and dD was better than ±0.1 and ±0.4 per mil, respectively, based upon repeated measures of an internal standard (BW-1).
BCO-DMO Processing:
- modified parameter names (replaced spaces with underscores);
- separated Dates_of_collection field into Date_Start and Date_End (yyyy-mm-dd).