RESUMO
Carbon dioxide (CO2) stands as the primary driver of Earth's greenhouse effect, and it's suggested that the global contribution of CO2 emissions from lakes cannot be ignored. Despite the numerous estimations of CO2 fluxes from lakes, limited focus has been directed towards the carbon isotopes (δ13C) of dissolved CO2 in lake water. Particularly, the potential use of δ13C values in tracing the CO2 concentrations in lake water remains as an understudied area, warranting further exploration and investigation. In this study, we conducted an analysis of the concentrations and δ13C values of dissolved CO2 in 33 lakes located at the Tibetan Plateau, Chinese Loess Plateau, and Yangtze Plain (among which high-resolution spatial investigations were performed in 6 lakes through in-situ continuous monitoring). Our findings revealed spatial variations in both the CO2 concentrations and δ13C values in lakes. Additionally, notable differences are observed among lakes in different regions of China, with lakes in the Yangtze Plain exhibiting considerably higher CO2 concentrations, and the overall CO2 δ13C values in lakes on the Tibetan Plateau tend to be more positive, while those in lakes on the Chinese Loess Plateau tend to be more negative. The pH values, dissolved oxygen, and dissolved organic carbon are likely crucial factors influencing the CO2 concentrations and δ13C values in the lakes. Furthermore, lake water CO2 concentrations are negatively correlated with δ13C values of CO2 and dissolved inorganic carbon (DIC) both within a single lake with high spatial resolutions or in lake groups across different regions. These results highlight that the CO2/DIC δ13C values can be applied to trace the concentration variations of dissolved CO2 in lakes.
RESUMO
Lakes are important sources of methane (CH4), and understanding the influence of environmental factors on CH4 concentration in lake water is crucial for accurately assessing CH4 emission from lakes. In this study, we investigated CH4 concentration in two connected Tibetan Plateau lakes, Lake Keluke (an open freshwater lake) and Lake Tuosu (a closed saline lake), through in-situ continuous measurements taken in different months from 2021 to 2023. The results show substantial spatial and seasonal variations in CH4 concentrations in the two lakes, while the CH4 concentrations in Lake Keluke are consistently higher than those in Lake Tuosu for each month. Despite sharing similar environmental conditions due to connected (e.g. pH, water temperature, dissolved oxygen content, and total organic carbon content), the critical difference between the two lakes is their salinity. This implies that salinity is the critical factor contributing to the decrease in CH4 concentrations in Lake Tuosu, possibly due to the changes in microbial species between freshwater and brackish/saline lakes. Additionally, to further validate the effect of salinity on CH4 concentrations in lake water, we compared the CH4 concentrations of 33 lakes (including 5 saline lakes and 28 freshwater lakes) from the Tibetan Plateau, Chinese Loess Plateau, and Yangtze Plain, and found that saline lakes consistently exhibit lower CH4 concentrations (avg. 0.08 µmol/L), while freshwater lakes generally display higher CH4 concentrations (avg. 1.25 µmol/L) with considerable fluctuations. Consequently, freshwater and saline lakes exhibit distinct CH4 emissions, which could be used for more accurate estimation of global CH4 emission from lakes.
RESUMO
Substantial nutrient inputs from reservoir impoundment typically increase sedimentation rate and primary production. This can greatly enhance methane (CH4) production, making reservoirs potentially significant sources of atmospheric CH4. Consequently, elucidating CH4 emissions from reservoirs is crucial for assessing their role in the global methane budget. Reservoir operations can also influence hydrodynamic and biogeochemical processes, potentially leading to pronounced spatiotemporal heterogeneity, especially in reservoirs with complex tributaries, such as the Three Gorges Reservoir (TGR). Although several studies have investigated the spatial and temporal variations in CH4 emissions in the TGR and its tributaries, considerable uncertainties remain regarding the impact of reservoir operations on CH4 dynamics. These uncertainties primarily arise from the limited spatial and temporal resolutions of previous measurements and the complex underlying mechanisms of CH4 dynamics in reservoirs. In this study, we employed a fast-response automated gas equilibrator to measure the spatial distribution and seasonal variations of dissolved CH4 concentrations in XXB, a representative area significantly impacted by TGR operations and known for severe algal blooms. Additionally, we measured CH4 production rates in sediments and diffusive CH4 flux in the surface water. Our multiple campaigns suggest substantial spatial and temporal variability in CH4 concentrations across XXB. Specifically, dissolved CH4 concentrations were generally higher upstream than downstream and exhibited a vertical stratification, with greater concentrations in bottom water compared to surface water. The peak dissolved CH4 concentration was observed in May during the drained period. Our results suggest that the interplay between aquatic organic matter, which promotes CH4 production, and the dilution process caused by intrusion flows from the mainstream primarily drives this spatiotemporal variability. Importantly, our study indicates the feasibility of using strategic reservoir operations to regulate these factors and mitigate CH4 emissions. This eco-environmental approach could also be a pivotal management strategy to reduce greenhouse gas emissions from other reservoirs.