B13E-0237:
The reactivity of plant-derived organic matter in the Amazon River and implications on aquatic carbon fluxes to the atmosphere and ocean

Monday, 15 December 2014
Nicholas D Ward1, Henrique O Sawakuchi2, Richard G Keil3, Rodrigo da Silva4, Daimio C Brito5, Alan C Cunha5, William Gagne-Maynard3, Aline de Matos6, Vania Neu7, Thomas S Bianchi8, Alex V Krusche2 and Jeffrey E Richey3, (1)University of Florida, Geological Sciences, Ft Walton Beach, FL, United States, (2)USP University of Sao Paulo, São Paulo, Brazil, (3)University of Washington, Seattle, WA, United States, (4)Universidade Federal do Oeste do Pará, Santarem, Brazil, (5)Universidade Federal do Amapá, Macapa, Brazil, (6)INPE National Institute for Space Research, Sao Jose dos Campos, Brazil, (7)Universidade Federal Rural da Amazônia, Belem, Brazil, (8)University of Florida, Gainesville, FL, United States
Abstract:
The remineralization of terrestrially-derived organic carbon (OC), along with direct CO2 inputs from autochthonous plant respiration in floodplains, results in an evasive CO2 gas flux from inland waters that is an order of magnitude greater than the flux of OC to the ocean. This phenomenon is enhanced in tropical systems as a result of elevated temperatures and productivity relative to temperate and high-latitude counterparts. Likewise, this balance is suspected to be influenced by increasing global temperatures and alterations to hydrologic and land use regimes.

Here, we assess the reactivity of terrestrial and aquatic plant-derived OM near the mouth of the Amazon River. The stable isotopic signature of CO213CO2) was monitored in real-time during incubation experiments performed in a closed system gas phase equilibration chamber connected to a Picarro Cavity Ring-Down Spectrometer. Incubations were performed under natural conditions and with the injection of isotopically labeled terrestrial macromolecules (e.g. lignin) and algal fatty acids. Under natural conditions, δ13CO2 became more depleted, shifting from roughly -23‰ to -27‰ on average, suggesting that C3 terrestrial vegetation was the primary fuel for CO2 production. Upon separate injections of 13C-labeled lignin and algal fatty acids, δ13CO2 increased near instantaneously and peaked in under 12 hours. Roughly 75% of the labeled lignin was converted to CO2 at the peak in δ13CO2, whereas less than 20% of the algal fatty acids were converted to CO2 (preliminary data subject to change). The rate of labeled-OC remineralization was enhanced by the addition of a highly labile substrate (e.g. ethyl acetate). Likewise, constant measurements of O2/pCO2 along the lower river revealed anomalously high CO2 and low O2 levels near the confluence of the mainstem and large tributaries with high algal productivity. These collective results suggest that the remineralization of complex terrestrial macromolecules is a significant source of CO2 to tropical rivers, whereas algal-derived OC is primarily incorporated into the microbial loop/higher trophic levels and enhances the breakdown of more complex terrestrially-derived molecules (e.g. the “priming effect”).