Supplemental Information Evidence that temperature does not influence the decomposition of organic carbon in forest mineral soils Christian P. Giardina* and Michael G. Ryan† *Department of Agronomy and Soil Science, Hawaii Branch Station, University of Hawaii at Manoa, 461 West Lanikaula Street, Hilo, Hawaii 96720 USA. Phone: 808-974-4105, FAX: 808-974-4110, e-mail: giardina@hawaii.edu †United States Department of Agriculture-Forest Service. Rocky Mountain Research Station. 240 West Prospect Street, Fort Collins, Colorado 80526 USA and Graduate Degree Program in Ecology, Colorado State University, Fort Collins, CO 80523. Phone: 970-498-1012, FAX: 970-498-1010, e-mail: mryan@lamar.colostate.edu Table 1. For these studies, soils were collected from the field, processed similarly, and analyzed for changes in 13 C natural abundance by mass spectrometry (details provided in original references). Most studies used adjacent forest stands to estimate the quantity of C3-C contained in pre-conversion soils. The loss of forest-derived Cs was then calculated from total Cs, bulk density, and % C3-C from standard mixing equations1. Results are given as turnover times estimated assuming 1st order decay as: -x / natural log of (Ct=x/ Ct=0) where C is the quantity of C3-C at time t, and x the number of years since conversion to C4 plant cover2,3. These estimates of turnover time are to be viewed as relative indexes of Cs turnover. For C3-C losses at the Laupahoehoe and Pepeekeo sites, Ct=0 was assumed to equal total C at t = x, because soils similar to these have been shown to lose or gain little total Cs with changes in land use1,4, and because the nearest forested sites were at different elevations. The turnover time for the 7 yr old Para, Brazil site 5 is underestimated because total Cs was assumed to be of 100% C3 origin in 1987, when the already 18-yrold abandoned pasture was disk-harrowed and re-seeded to C4 pasture grasses. Variations in temperature and soil clay content were unrelated to Cs turnover. However, the variation in Cs turnover times among sites may be attributed to differences in time since conversion, moisture, Cs quality, or management. Table 2. Soils were collected from closed canopy forests, processed similarly, placed into sealable containers, and maintained at controlled moisture and temperature levels for the duration of the incubation (details provided in original references). The release of CO2 was estimated by titrating sodium hydroxide traps to measure the quantity of CO2 absorbed per unit of time18-20, by measuring changes in [CO2] per unit of time in the head space of the containers by gas chromatography21, or by measuring changes in the Cs content of the incubated soil22. The unpublished data Paustian et al. are based on the sodium hydroxide trap approach. Paustian et al. incubated soils for 10 months, so release curves for these two points were fit with an exponential equation to estimate Cs release at 12 months. Similar quantities of Cs were lost from the two Yurimaguas Paleudults and the North Carolina Arenic Paleudult, suggesting that the different laboratory methods reviewed here give comparable estimates of Cs decomposition rates. In these studies, soil moisture was similar across incubations while temperature and soil clay content varied. Litter-quality also varied across sites, but with no observable effects on Cs quality. For example, the Wisconsin sites supported trees with widely ranging litter quality, but Cs decomposition rates did not vary substantially. References 1. Bashkin, M. & Binkley, D. Changes in soil carbon following afforestation in Hawaii. Ecology 79, 828-833 (1998). 2. Gregorich, E. G., Ellert, B. H. & Monreal, C. M. Turnover of soil organic matter and storage of corn residue C estimated from C-13 abundance. Can. J. Soil Sci. 75, 161167 (1995). 3. Paul, E. & Clark F. Soil Microbiology and Biochemistry (Academic Press, New York 1996). 4. Binkley, D. & Resh, S. C. Rapid changes in soils following Eucalyptus afforestation in Hawaii. Soil Sci. Soc. Amer. J. 63, 222-225 (1999). 5. Trumbore, S.E. et al. Belowground cycling of carbon in forests and pastures of Eastern Amazonia. Global Biogeochem. Cycles 9, 515-528 (1995). 6. Balesdent, J., Mariotti, A. & Boisgontier, D. Effect of tillage on soil organic carbon mineralization estimated from 13C abundance in maize fields. J. Soil Sci. 41, 587-596 (1990). 7. Arrouays, D. et al. Modelling organic carbon turnover in cleared temperate forest soils converted to maize cropping by using 13C natural abundance measurements. Plant Soil 173,191-196 (1995). 8. Balesdent, J., Mariotti, A. & Guillet, B. Natural 13C abundance as a tracer for studies of soil organic matter dynamics. Soil Biol. Biochem. 19, 25-30 (1987). 9. Skjemstad, J., Le Feuvre, R. & Prebble, R. Turnover of soil organic matter under pasture as determined by (1990). 13 C natural abundance. Aust. J. Soil Res. 28, 267-276 10. Townsend, A. R., Vitousek, P. M. & Trumbore, S.E. Soil organic matter dynamics along gradients in temperature and land use on the Island of Hawaii. Ecology 76, 721733 (1995). 11. Vitorello, V. A. et al. Organic matter and natural C-13 distribution in forested and cultivated Oxisols. Soil Sci. Soc. Amer. J. 53, 773-778 (1989). 12. Cadisch, G. et al. Carbon turnover (13C) and nitrogen mineralization potential of particulate light soil organic matter after rainforest clearing. Soil Biol. Biochem. 28, 1555-1567 (1996). 13. Hsieh, Y. Soil organic C pools of two tropical soils inferred by carbon signatures. Soil Sci. Soc. Amer. J. 60, 1117-1121 (1996). 14. Trouve, C., Mariotti, A., Schwartz, D. & Guillet, B. Soil organic carbon dynamics under Eucalyptus and Pinus planted on savannas in the Congo. Soil Biol. Biochem. 26, 287-295 (1994). 15. Neill C. et al. Forest- and pasture-derived carbon contribution to carbon stocks and microbial respiration of tropical pasture soils. Oecologia 107, 113-119 (1996). 16. Veldkamp, E. Organic carbon turnover in three tropical soils under pasture after deforestation. Soil Sci. Soc. Amer. J. 58, 175-180 (1994). 17. Desjardins, T. et al. Organic carbon and 13 C contents in soil and soil size fractions, and their changes due to deforestation and pasture installation in eastern Amazonia. Geoderma 61, 103-108 (1994). 18. Motavalli, P. P. et al. Comparison of laboratory and modeling simulation methods for estimating soil carbon pools in tropical forest soils. Soil Biol. Biochem. 26, 935-944 (1994). 19. Giardina, C., M. Ryan, R. Hubbard, and D. Binkley. Effects of litter quality and clay content on carbon and nitrogen mineralization in Rocky Mountain soils. Ecology (in review). 20. Scott, N. A. Plant species effects on soil organic matter turnover and nutrient release in forest and grasslands, Ph.D. dissertation, Colorado State University, USA (1996). 21. Hart, S. C., Nason, G. E., Myrold, D. D. & Perry, D. A. Dynamics of gross nitrogen transformations in an old-growth forest: the carbon connection. Ecology 75, 880-891 (1994). 22. Muamba, T. F. Organic matter decomposition of contrasting soils in relation to resulting chemical fertility characteristics, M.S. thesis, North Carolina State University, USA (1992).