Seasonal changes in the abundance and composition of plant pigments in particulate organic carbon in the lower Mississippi and Pearl Rivers

Plant pigments in particulate organic carbon were examined in the lower Mississippi and Pearl Rivers (U.S.), along with physical variables and nutrients to study seasonal changes in the abundance and composition of phytoplankton. Water samples were collected monthly from September 2001 to August 2003 in the lower Mississippi River (MR; no samples were taken in February 2002) and from August 2001 to July 2003 in the Pearl River (PR). High concentrations of total suspended solids (TSS), nutrients, and chlorophyll a (chl a; dominated by diatoms) were observed in the lower MR. The smaller blackwater PR was characterized by lower nutrients and chl a, higher ultraviolet absorbance, and a phytoplankton biomass dominated by chlorophytes. Chl a concentrations in the lower MR was high in summer low-flow periods and also during interims of winter and spring, and did not couple with physical variables and nutrients, likely due to a combination of in situ production and inputs from reservoirs, navigation locks, and oxbow lakes in the upper MR and Missouri River. Chl a concentrations in the PR was only high in summer low-flow periods and were controlled by temperature and concentrations of chromophoric dissolved organic matter (CDOM). The high, diatom-dominated phytoplankton biomass in the lower MR was likely the result of decreasing TSS (increased damming in the watershed) and increasing nutrients (enhanced agricultural runoff) over the past few decades. Lower phytoplankton biomass (dominated by chlorophytes) in the PR was likely linked with intense shading by CDOM and lower availability of nutrient inputs. An increase in the relative importance of phytoplankton biomass in large turbid rivers, such as the MR, could have significant effects on the age and lability of riverine organic matter entering the ocean, the stoichiometric balance of nutrients delivered to coastal margins, and the sequestration of atmospheric CO(2) in these dynamic regions.