When river meets ocean: distribution and conversion of suspended organic particles in a Sundarbans mangrove river-estuary system, Bangladesh

Global carbon cycle has received extensive attention,among which the river-estuary system is one of the important links connecting the carbon cycle between land and ocean.In this paper,the distribution and control factors of particulate organic carbon(POC)were studied by using the data of organic carbon contents and its carbon isotopic composition(δ13C)in the mainstream and estuary of Passur River in the Sundarbans area,combined with the hydrological and biological data measured by CTD.The results show that POC content ranged from 0.263 mg/L to 9.292 mg/L,and the POC content in the river section(averaged 4.129 mg/L)was significantly higher than that in the estuary area(averaged 0.858 mg/L).Two distinct stages of POC transport from land to sea in the Sundarbans area were identified.The first stage occurred in the river section,where POC distribution was mainly controlled by the dynamic process of runoff and the organic carbon was mainly terrestrial source.The second stage occurred during estuarine mixing,where the POC distribution was mainly controlled by the mixing process of seawater and freshwater.The source of POC was predominantly marine and exhibiting vertical differences.The surface and middle layers were primarily influenced by marine sources,while the bottom layer was jointly controlled by terrestrial and marine sources of organic carbon.These findings are of great significance for understanding the carbon cycle in such a large mangrove ecosystem like the Sundarbans mangrove.

Chemical characteristics of PM_(2.5) during haze episodes in the urban of Fuzhou,China

Atmospheric fine particles （PM2.5） were collected in this study with middle volume samplers in Fuzhou, China, during both normal days and haze days in summer （September 2007） and winter （january 2008）. The concentrations, distributions, and sources of polycyclic aromatic hydrocarbons （PAHs）, organic carbon （OC）, elemental carbon （EC）, and water soluble inorganic ions （WSIls） were determinated. The results showed that the concentrations of PM2.s, PAHs, OC, EC, and WSIIs were in the orders of haze 〉 normal and winter〉 summer. The dominant PAHs of PM2.s in Fuzhou were Fluo, Pyr, Chr, BbF, BkF, BaP, BghiP, and IcdP, which represented about 80.0% of the total PAHs during different sampling periods. The BaPeq concentrations of ^-~PAHs were 0.78, 0.99, 1.22, and 2.43 ng/m3 in summer normal, summer haze, winter normal, and winter haze, respectively. Secondary pollutants （SO42 , NO3 , NH4＊, and OC） were the major chemical compositions of PM2.5, accounting for 69.0%, 55.1%, 63.4%, and 64.9% of PM2.s mass in summer normal, summer haze, winter normal, and winter haze, respectively. Correspondingly, secondary organic carbon （SOC） in Fuzhou accounted for 20.1%, 48.6%, 24.5%, and 50.5% of OC. The average values of nitrogen oxidation ratio （NOR） and sulfur oxidation ratio （SOR） were higher in haze days （0.08 and 0.27） than in normal days （0.05 and 0.22）. Higher OC/EC ratios were also found in haze days （5.0） than in normal days （3.3）. Correlation analysis demonstrated that visibility had positive correlations with wind speed, and neg- ative correlations with relative humidity and major air pollutants. Overall, the enrichments of PM2.5, OC, EC, SO42 ,andNO3 promoted haze formation. Furthermore, the diagnostic ratios of IcdP/（IcdP ＋ BghiP）, lcdP/BghiP, OC/EC, and NO3 /SO42 indicated that vehicle exhaust and coal consumption were the main sources of pollutants in Fuzhou.