Sanderman and KramerDOM production and chemistry
Supplemental Material
Supplemental Table 1. Initial characteristics of soils used in leaching experiment.
Site1 / Horizon / Thickness2 (cm) / Mass2 (g) / Carbon(%) / Nitrogen (%) / C/N ratio / Lignin3 (%) / Lignin/N ratio
Thurston, Hawai’i
(0.3 ky) / O / 4.7 / 39.8 / 47.5 / 1.15 / 42.2 / 29.1 / 25.3
Oie / 2.0 / 12.0 / 48.7 / 0.95 / 51.3 / 26.1 / 16.9
Oa / 2.7 / 25.7 / 47.0 / 1.24 / 37.9 / 31.8 / 15.6
Laupahoehoe, Hawai’i
(20 ky) / O / 7.4 / 73.2 / 36.4 / 1.48 / 24.8 / 25.0 / 13.8
Oie / 1.8 / 11.1 / 51.4 / 1.39 / 36.9 / 22.6 / 18.9
Oa / 6.5 / 62.2 / 33.8 / 1.49 / 22.6 / 35.0 / 25.6
Pu’u Eke, Hawai’i
(350 ky) / O / 6.7 / 69.8 / 45.1 / 1.72 / 28.0 / 26.9 / 23.5
Oie / 1.9 / 12.8 / 42.8 / 0.96 / 44.7 / 25.8 / 14.6
Oa / 5.2 / 56.2 / 45.7 / 1.89 / 24.2 / 27.6 / 14.4
Pu’uKolekole, Moloka’i
(1400 ky) / O / 8.7 / 86.7 / 50.5 / 1.52 / 33.8 / 21.0 / 18.6
Oie / 2.0 / 13.9 / 49.1 / 1.10 / 44.6 / 18.8 / 27.5
Oa / 7.0 / 66.6 / 50.8 / 1.61 / 31.6 / 23.2 / 16.3
Koke’e,
Kaui
(4100 ky) / O / 7.9 / 111.5 / 44.6 / 1.76 / 26.5 / 33.2 / 26.9
Oie / 2.0 / 13.6 / 53.4 / 1.10 / 48.6 / 32.1 / 17.1
Oa / 6.9 / 102.5 / 43.4 / 1.84 / 23.6 / 34.3 / 29.2
1Substrate age given in parentheses
2Mean thickness and mass of packed cores for leaching experiment
3Percent lignin determined by applying a molecular mixing model to 13C NMR results
Supplemental Figure 1. Time series of horizon averaged CO2 fluxes (A) and DOC concentration in core leachates (B). Error bars indicate one standard error (n = 15).
Supplemental Table 2. Percent distribution of signal intensity across major shift regions and results from molecular mixing model for NMR spectra shown in Figure 3.
Shift region / Major C type / Th (0.3) / La (20) / Pu (350) / Mo (1400) / Ko (4100) / Th (0.3) / La (20) / Pu (350) / Mo (1400) / Ko (4100)Oie horizon organic material / DOM effluent from whole O core
0 - 45 / Alkyl / 23.3 / 14.5 / 24.6 / 16.8 / 22.9 / 27.0 / 25.5 / 27.7 / 23.4 / 24.9
45 - 60 / N-Alkyl/Methoxyl / 10.1 / 8.6 / 11.9 / 7.6 / 10.5 / 10.7 / 10.0 / 10.7 / 10.1 / 10.1
60 - 95 / O-Alkyl / 39.8 / 45.8 / 37.0 / 42.0 / 33.6 / 26.0 / 24.9 / 24.3 / 25.5 / 24.4
95 - 110 / Di-O-Alkyl / 9.7 / 10.8 / 9.2 / 11.3 / 12.2 / 6.2 / 6.5 / 6.4 / 7.0 / 7.0
110 - 145 / Aromatic / 10.3 / 11.6 / 9.2 / 13.6 / 9.8 / 13.1 / 13.5 / 12.8 / 14.5 / 13.1
145 - 165 / Phenolic / 4.2 / 4.2 / 4.6 / 5.0 / 6.1 / 5.0 / 5.9 / 5.4 / 5.9 / 5.6
165 - 215 / Amide/Carboxyl / 2.6 / 4.6 / 3.5 / 3.5 / 4.9 / 12.0 / 13.9 / 12.6 / 13.7 / 15.0
Molecular Mixing Model Component / Carbohydrate / 50.6 / 57.6 / 45.6 / 39.9 / 40.5 / 27.1 / 25.6 / 25.0 / 26.3 / 25.0
Protein / 6.3 / 8.8 / 9.2 / 10.4 / 11.5 / 8.8 / 11.7 / 10.7 / 11.8 / 11.2
Lignin / 26.1 / 27.0 / 25.8 / 18.8 / 32.1 / 31.6 / 31.5 / 31.4 / 33.6 / 30.8
Lipid / 17.0 / 6.4 / 19.4 / 30.9 / 16.0 / 20.9 / 17.6 / 20.9 / 14.9 / 16.9
Carbonyl / 0.0 / 0.3 / 0.0 / 0.0 / 0.0 / 11.7 / 13.6 / 11.9 / 13.3 / 16.1
Supplemental Table 3.Percent distribution of major biomolecular components based upon NMR-molecular mixing model results from litter and DOM samples collected from a range of ecosystem types.
Litter type / Carbohydrate / Protein / Lignin / Lipid / CarbonylLitter samples
Ohi'a forest / 1 / 48.1 / 4.9 / 38.2 / 7.5 / 1.3
Redwood-Douglas fir / 2 / 46.8 / 7.2 / 26.0 / 17.9 / 2.1
Mixed grassland / 2 / 71.3 / 8.3 / 16.6 / 2.6 / 1.2
Eucalyptus globulus / 3 / 40.9 / 7.9 / 31.4 / 9.8 / 10.0
Wheat residues / 3 / 61.5 / 10.5 / 17.8 / 3.6 / 6.6
DOM samples
Ohi'a forest / 1 / 25.8 / 10.8 / 31.8 / 18.2 / 13.3
Redwood-Douglas fir / 2 / 26.5 / 6.3 / 35.3 / 12.7 / 19.2
Mixed grassland / 2 / 24.9 / 14.2 / 40.1 / 4.1 / 16.7
Eucalyptus globulus / 3 / 21.4 / 9.0 / 39.7 / 13.8 / 16.4
Wheat residues / 3 / 28.8 / 18.6 / 29.9 / 13.0 / 11.7
1 mean value across all 5 sites in this study
2 Sanderman et al. (2008)
3 Sanderman (unpublished)
Supplement Table 4. Bioavailability experiment results.
Initial characteristics / Final characteristicsSite / Horizon / DOCa
(mg L-1) / SUVA (L mg C-1 m-1) / DOC/DON / Al (mg L-1) / C mass loss
(%) / SUVA (L mg C-1 m-1)
Th / O / 51.4± 12.5 / 4.37 ± 0.16 / 35.8± 5.8 / 0.49 ± 0.16 / 10.3± 7.4 / 4.90± 0.13
Oie / 32.2± 9.0 / 3.86 ± 0.13 / 54.7 ± 3.5 / 0.12 ± 0.03 / 16.7 ± 2.3 / 4.57 ± 0.1
Oa / 34.7 ± 9.2 / 4.68 ± 0.10 / 42.1 ± 17.0 / 0.62 ± 0.13 / 8.6± 2.2 / 5.17 ± 0.07
La / O / 113.9± 28.7 / 4.22 ± 0.12 / 11.2 ± 7.0 / 0.93 ± 0.44 / 9.6 ± 8.6 / 4.85 ± 0.45
Oie / 86.0± 15.8 / 4.03 ± 0.04 / 34.2 ± 13.1 / 0.26 ± 0.10 / 2.4 ± 1.4 / 4.18 ± 0.22
Oa / 101.9± 30.0 / 4.45 ± 0.16 / 10.9 ± 3.8 / 1.24 ± 0.17 / 0.0± 1.9 / 4.66 ± 0.1
Pu / O / 86.0± 15.8 / 4.03 ± 0.04 / 22.3 ± 2.2 / 0.73 ± 0.20 / 2.4 ± 1.4 / 4.18 ± 0.22
Oie / 69.1± 23.9 / 4.14 ± 0.19 / 44.0 ± 14.6 / 0.21 ± 0.04 / 16.4 ± 0.9 / 5.00± 0.21
Oa / 113.8 ± 33.4 / 4.52 ± 0.20 / 22.3 ± 1.0 / 0.65 ± 0.07 / 9.8± 4.6 / 5.20± 0.28
Mo / O / 168.5 ± 29.9 / 4.55 ± 0.07 / 24.1 ± 2.5 / 0.42 ± 0.14 / 9.1± 2.2 / 5.20± 0.17
Oie / 98.5 ± 12.0 / 4.53 ± 0.47 / 34.4 ± 15.8 / 0.24 ± 0.17 / 13.2 ± 8.3 / 5.20± 0.08
Oa / 106.7 ± 40.5 / 4.93 ± 0.64 / 42.5 ± 22.6 / 0.35 ± 0.18 / 10.8 ± 10.1 / 5.79 ± 0.2
Ko / O / 77.1 ± 17.5 / 4.49 ± 0.29 / 27.0 ± 7.1 / 0.63 ± 0.28 / 6.6± 1.4 / 5.04 ± 0.25
Oie / 49.3 ± 8.2 / 4.17 ± 0.19 / 40.8 ± 10.3 / 0.01 ± 0.06 / 19.5 ± 4.5 / 5.10± 0.09
Oa / 75.9 ± 38.9 / 4.76 ± 0.13 / 30.9 ± 6.8 / 0.66 ± 0.25 / 6.4± 2.7 / 5.25 ± 0.21
a initial value before dilution to approximately 30 mg C L-1
1