119 - In situ electrochemical techniques for discerning fluxes in surficial permeable sediments
Brian T Glazer1, firstname.lastname@example.org, Francis J Sansone1, Jonathon P Fram2, Eugene R Pawlak3, Angelos Hannides1, Kristen Fogaren1, Jennifer Murphy1. (1) Department of Oceanography, University of Hawaii, Honolulu, HI 96822, United States, (2) College of Earth, Ocean and Atmospheric Sciences, Oregon State University, Corvallis, OR 97331, United States, (3) Jacobs School of Engineering, University of California, San Diego, San Diego, CA 92093, United States
The upper layers of nearshore permeable sediments are dynamic, active sites of intense redox cycling. Previous research and our preliminary results indicate that vertical redox oscillations in these sediments can be driven by biogeochemical or physical variability, or by episodic events such as severe storms and their associated terrestrial runoff. Further, it can be assumed that each of these forcings operate on distinctive time and spatial scales. The current work focuses on central goals of calculating the fluxes of redox-sensitive chemical species in surficial permeable coastal sediments, and understanding the transformations within the highly responsive zone of reactivity in the upper centimeters of these sediments. Here, we describe recent efforts to: (i) improve understanding of the interaction between active, carbon recycling sediments and the overlying water column; (ii) examine the variability of key chemical species; (iii) quantify the relative contributions of benthic photosynthesis, sand ripple position, currents and waves to redox oscillations; and (iv) integrate fine-scale chemical measurements with porewater velocity modeling to calculate biogeochemical fluxes.
Tuesday, April 9, 2013 02:00 PM
Biogeochemical Transformation of Transition Elements in Aquatic Systems: A Symposium in Honor of George W. Luther's Accomplishments in Geochemistry (01:30 PM - 04:35 PM)
Location: Morial Convention Center