Priming of terrestrially-derived dissolved organic matter: Implications for coastal carbon cycling

Thomas S S Bianchi1, Nicholas D Ward1, Daniel C Thornton2, Shari Ann Yvon-Lewis3, Gary King4, Michael R Shields5, Timothy I Eglinton6 and Jason H Curtis7, (1)University of Florida, Geological Sciences, Ft Walton Beach, FL, United States, (2)Texas A&M University, Dept. of Oceanography, College Station, TX, United States, (3)Texas A & M University College Station, College Station, TX, United States, (4)Louisiana State University, Biological Sciences, Baton Rouge, LA, United States, (5)University of Florida, Department of Geological Sciences, Gainesville, FL, United States, (6)ETH Zürich, Geologisches Institut, Zurich, Switzerland, (7)University of Florida, Geological Sciences, Gainesville, United States

Contact First Author: Thomas S S Bianchi; tbianchi@ufl.edu

Abstract ID#: 36162

 

English Abstract:
<span'',serif;">Although inland waters comprise a small fraction of Earth’s surface, they play a critical role in the global C cycle. Global estimates of riverine flux of dissolved organic carbon (DOC) to the oceans range from about 250 to 360 Tg y-1. Interestingly, only a small fraction of the roughly 2900 Tg C yr-1 transported through inland waters globally ever reaches the ocean. Recent observations of immense CO2 evasion from streams and rivers thus suggest that terrestrially-derived DOC (TDOC) is not as recalcitrant as previously thought. In a lab-based experiment pine-litter leachate was converted to CO2 at roughly the same rate in the trehalose and diatom leachate treatments, less than 1% of the diatom leachate was converted to CO2, as opposed to ~50% of the trehalose over a few days. It is likely that a large fraction of the diatom leachate was assimilated by bacteria, whereas the trehalose was mostly respired to CO2. Pilot field experiments in the Amazon River, with the incubation system performed during two cruises show that δ13CO2 rapidly increased after adding labeled lignin; roughly 50% of the added lignin was converted to CO2 in 10 hours. This is equivalent to a remineralization rate of ~0.021 mg C L-1d-1, or 2x the rate of FACE-only remineralization measured in the lab experiments.