Cycling of suspended particulate phosphorus in the redoxcline of the Cariaco Basin

Published in Marine Chemistry , v. 176:64-74 
Authors

McParland, E., Benitez-Nelson, C.R., Taylor, G.T., Thunell, R., Rollings, A. and Lorenzoni, L.

Publication year 2015
DOI https://doi.org/10.1016/j.marchem.2015.07.008
Affiliations
  • Marine and Environmental Biology Program, 3616 Trousdale Parkway, University of Southern California, Los Angeles, CA 90089, USA
  • Marine Science Program & Department of Earth and Ocean Sciences, University of South Carolina, Columbia, SC 29208, USA
  • School of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook, NY 11794, USA
  • College of Marine Science, University of South Florida, St. Petersburg, FL, USA

 

IAI Program

CRN3

IAI Project CRN3035
Keywords

Abstract

The Cariaco Basin, located off the coast of Venezuela, is anoxic below ~ 250 m and has a productive redoxcline where several chemical gradients support multiple biogeochemical reactions. Thus, the Cariaco Basin is an ideal study site for investigating how redox chemistry influences phosphorus (P) biogeochemistry across oxic/anoxic boundaries. While sinking particles in the Cariaco Basin have been investigated previously for P composition and flux, this is the first study to describe P within suspended particulate particles, a key phase connecting particulate and dissolved P pools. Analysis of samples collected between April 2008 and April 2012, indicates that secondary peaks in total suspended particulate P (TSPP) concentrations (88 ± 60 nM) were present in the redoxcline and were similar in magnitude to those measured in the upper 100 m (84 ± 77 nM TSPP). However, the composition of TSPP was significantly different between the surface and the redoxcline. Suspended soluble reactive phosphorus (SSRP) was on average 3 ± 2 times greater in the redoxcline than observed in surface waters. Furthermore, composition of the TSPP pool significantly changed from less biologically available P forms (~ 45% organic P) above and below the redoxcline to more biologically available P forms (~ 80% loosely/oxide-bound P) within the redoxcline. We argue that the abrupt increases and transformations in the TSPP pool within the redoxcline result from both abiotic reactions associated with a manganese and iron redox shuttle and biotic reactions associated with a large and diverse chemoautotrophic prokaryotic community. These results suggest that the biogeochemical cycling of P may be altered within oxygen depleted water columns in unexpected ways.