Sources and fluxes of particulate organic carbon in the Wujiang cascade reservoirs, southwest China

Inland Waters ◽  
2018 ◽  
Vol 8 (2) ◽  
pp. 141-147 ◽  
Author(s):  
Jie Shi ◽  
Baoli Wang ◽  
Fushun Wang ◽  
Xi Peng
2021 ◽  
Author(s):  
Yuanyuan Zhang ◽  
Youheng Su ◽  
Zhe Li ◽  
Shuhui Guo ◽  
Lunhui Lu ◽  
...  

Abstract. Methane (CH4) emissions from freshwaters to the atmosphere have a profound impact on global atmospheric greenhouse gas (GHG) concentrations. Anthropogenic footprints such as dam construction and reservoir operation significantly changed the fate and transport of CH4 in freshwaters. The type of particulate organic carbon (POC) in reservoirs is a critical factor controlling CH4 production and emissions. However, little is known of how reservoir operation mediates the distribution of POC and regulates CH4 accumulation in cascade hydroelectric reservoirs. Here, spatial and temporal variations in POC and CH4 were explored in the Xiluodu (XLD) and Xiangjiaba (XJB) reservoirs which are deep valley dammed cascade reservoirs located in the main channel of the upper Yangtze River. Based on the δ13C-POC and N / C mole ratios of particulate organic matter, the results of multi-endmember stable isotope mixing models by a Bayesian model show that terrestrial POC and autochthonous POC accounted for approximately 56 ± 19 % and 42 ± 19 % (SD, n = 181) of POC, respectively. CH4 concentrations and δ13C-CH4 in the cascade reservoirs were potentially influenced by CH4 oxidation. Together with other physicochemical parameters and structural equation model, these results suggested that the input of terrestrial POC was dominantly influenced by water level variations and flow regulation due to reservoir operation. The cumulative effect of POC caused by cascade reservoirs was not apparent at a bimonthly scale. Terrestrial POC was more likely to dominate CH4 accumulation in cascade reservoirs under reservoir operation.


2019 ◽  
Author(s):  
Michael Stukel ◽  
Thomas Kelly

Thorium-234 (234Th) is a powerful tracer of particle dynamics and the biological pump in the surface ocean; however, variability in carbon:thorium ratios of sinking particles adds substantial uncertainty to estimates of organic carbon export. We coupled a mechanistic thorium sorption and desorption model to a one-dimensional particle sinking model that uses realistic particle settling velocity spectra. The model generates estimates of 238U-234Th disequilibrium, particulate organic carbon concentration, and the C:234Th ratio of sinking particles, which are then compared to in situ measurements from quasi-Lagrangian studies conducted on six cruises in the California Current Ecosystem. Broad patterns observed in in situ measurements, including decreasing C:234Th ratios with depth and a strong correlation between sinking C:234Th and the ratio of vertically-integrated particulate organic carbon (POC) to vertically-integrated total water column 234Th, were accurately recovered by models assuming either a power law distribution of sinking speeds or a double log normal distribution of sinking speeds. Simulations suggested that the observed decrease in C:234Th with depth may be driven by preferential remineralization of carbon by particle-attached microbes. However, an alternate model structure featuring complete consumption and/or disaggregation of particles by mesozooplankton (e.g. no preferential remineralization of carbon) was also able to simulate decreasing C:234Th with depth (although the decrease was weaker), driven by 234Th adsorption onto slowly sinking particles. Model results also suggest that during bloom decays C:234Th ratios of sinking particles should be higher than expected (based on contemporaneous water column POC), because high settling velocities minimize carbon remineralization during sinking.


Nature ◽  
1977 ◽  
Vol 266 (5604) ◽  
pp. 713-716 ◽  
Author(s):  
S. KRISHNASWAMI ◽  
D. LAL

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