ALBERT

Description: Optical measurements using ultra-violet/visible (UV/Vis) spectrophotometric sensors and fluorescent dissolved organic matter (FDOM) sensors have recently been used as proxies of dissolved organic carbon (DOC) concentrations of streams and rivers at high temporal resolution. Despite of the merits of the sensors, temperature changes and particulate matter in water can interfere the sensor readings, over- or under-estimating DOC concentrations. However, little efforts have been made to compare responses of the two types of the sensors in natural conditions. We conducted both laboratory experiments and in situ monitoring with a UV/Vis sensor and a FDOM sensor during the three storm events in the fall of 2012 and the spring of 2013 in a forest stream in Korea in order to compare their performance. Laboratory experiments using the Suwannee River natural organic matter, humic acid, and fulvic acid demonstrated strong linear relationships between both the sensor signals and measured DOC concentrations with R2 ≥ 0.98. Although temperature compensation might not be needed for the UV/Vis sensor, it was sensitive to relativley small changes in turbidity. In contrast, the FDOM sensor was insenstive to relatively low turbidity while the FDOM sensor outputs decreased significantly as temperature increased, requiring temperature compensated FDOM (e.g. FDOM20 for 20 °C) for in situ monitoring of DOC. The results suggest that both sensors can be employed as a~proxy for stream DOC concentrations after temperature and turbidity compensation in a forest stream where terrestrially derived humic-like materials are dominant components.

Description: The source and sinks of carbon dioxide (CO2) and methane (CH4) due to anthropogenic and natural biospheric activities were estimated for the South Asia region (Bangladesh, Bhutan, India, Nepal, Pakistan and Sri Lanka). Flux estimates were based on top-down methods that use inversions of atmospheric data, and bottom-up methods that use field observations, satellite data, and terrestrial ecosystem models. Based on atmospheric CO2 inversions, the net biospheric CO2 flux in South Asia (equivalent to the Net Biome Productivity, NBP) was a sink, estimated at −104 ± 150 Tg C yr−1 during 2007–2008. Based on the bottom-up approach, the net biospheric CO2 flux is estimated to be −191 ± 193 Tg C yr−1 during the period of 2000–2009. This last net flux results from the following flux components: (1) the Net Ecosystem Productivity, NEP (net primary production minus heterotrophic respiration) of −220 ± 186 Tg C yr−1 (2) the annual net carbon flux from land-use change of −14 ± 50 Tg C yr−1, which resulted from a sink of −16 Tg C yr−1 due to the establishment of tree plantations and wood harvest, and a source of 2 Tg C yr−1 due to the expansion of croplands; (3) the riverine export flux from terrestrial ecosystems to the coastal oceans of +42.9 Tg C yr−1; and (4) the net CO2 emission due to biomass burning of +44.1 ± 13.7 Tg C yr−1. Including the emissions from the combustion of fossil fuels of 444 Tg C yr−1 for the decades of 2000s, we estimate a net CO2 land-to-atmosphere flux of 297 Tg C yr−1. In addition to CO2, a fraction of the sequestered carbon in terrestrial ecosystems is released to the atmosphere as CH4. Based on bottom-up and top-down estimates, and chemistry-transport modeling, we estimate that 37 ± 3.7 Tg C-CH4 yr−1 were released to atmosphere from South Asia during the 2000s. Taking all CO2 and CH4 fluxes together, our best estimate of the net land-to-atmosphere CO2-equivalent flux is a net source of 334 Tg C yr−1 for the South Asia region during the 2000s. If CH4 emissions are weighted by radiative forcing of molecular CH4, the total CO2-equivalent flux increases to 1148 Tg C yr−1 suggesting there is great potential of reducing CH4 emissions for stabilizing greenhouse gases concentrations.

Description: The source and sinks of carbon dioxide (CO2) and methane (CH4) due to anthropogenic and natural biospheric activities were estimated for the South Asian region (Bangladesh, Bhutan, India, Nepal, Pakistan and Sri Lanka). Flux estimates were based on top-down methods that use inversions of atmospheric data, and bottom-up methods that use field observations, satellite data, and terrestrial ecosystem models. Based on atmospheric CO2 inversions, the net biospheric CO2 flux in South Asia (equivalent to the Net Biome Productivity, NBP) was a sink, estimated at −104 ± 150 Tg C yr−1 during 2007–2008. Based on the bottom-up approach, the net biospheric CO2 flux is estimated to be −191 ± 193 Tg C yr−1 during the period of 2000–2009. This last net flux results from the following flux components: (1) the Net Ecosystem Productivity, NEP (net primary production minus heterotrophic respiration) of −220 ± 186 Tg C yr−1 (2) the annual net carbon flux from land-use change of −14 ± 50 Tg C yr−1, which resulted from a sink of −16 Tg C yr−1 due to the establishment of tree plantations and wood harvest, and a source of 2 Tg C yr−1 due to the expansion of croplands; (3) the riverine export flux from terrestrial ecosystems to the coastal oceans of +42.9 Tg C yr−1; and (4) the net CO2 emission due to biomass burning of +44.1 ± 13.7 Tg C yr−1. Including the emissions from the combustion of fossil fuels of 444 Tg C yr−1 for the 2000s, we estimate a net CO2 land–atmosphere flux of 297 Tg C yr−1. In addition to CO2, a fraction of the sequestered carbon in terrestrial ecosystems is released to the atmosphere as CH4. Based on bottom-up and top-down estimates, and chemistry-transport modeling, we estimate that 37 ± 3.7 Tg C yr−1 were released to atmosphere from South Asia during the 2000s. Taking all CO2 and CH4 fluxes together, our best estimate of the net land–atmosphere CO2-equivalent flux is a net source of 334 Tg C yr−1 for the South Asian region during the 2000s. If CH4 emissions are weighted by radiative forcing of molecular CH4, the total CO2-equivalent flux increases to 1148 Tg C yr−1 suggesting there is great potential of reducing CH4 emissions for stabilizing greenhouse gases concentrations.