Greenhouse gas budgets of severely polluted urban lakes in India.

Inland waters are important sources of greenhouse gases and emissions from polluted subtropical systems may be contributing to the observed global increase in atmospheric methane concentrations. Here we detail a scoping study where dissolved concentrations of greenhouse gases methane (CH4), carbon dioxide (CO2) and nitrous oxide (N2O) were measured in two contrasting urban lakes in Bangalore (Bengaluru), Karnataka, India, from June 2018 to February 2020. Bellandur Lake is a severely polluted system whilst Jakkur Lake has been subject to partial restoration via treatment of organic matter inputs. Methane concentrations in Bellandur Lake were three orders of magnitude higher than in Jakkur Lake, with a mean concentration of 3.02 ± 1.57 mg CH4-C L-1 compared to 1.72 ± 1.22 µg CH4-C L-1. At Bellandur Lake, dissolved CO2 concentrations were of the same order of magnitude as for CH4, whereas at Jakkur Lake dissolved CO2 concentrations were two orders of magnitude greater than for CH4. Concentrations of N2O were negligible in both lakes. Extrapolating our data to estimate greenhouse gas fluxes, mean daily methane fluxes from Bellandur Lake were consistently in excess of 1000 mg CH4 m2 d-1, rendering the lake a source of GHGs to the order of 148,350 ± 21,790 ton yr-1 CO2-e yr-1, compared to 100 ± 37 ton CO2-e yr-1 from Jakkur Lake, with CH4 contributing primarily to this difference. We propose that the contribution of severely polluted urban lakes to global CH4 production warrants further investigation, particularly as our evidence suggests that standard secondary wastewater treatment to support restoration of these systems has the potential to significantly reduce CH4 emissions.

Effects of land use on surface-atmosphere exchanges of trace gases and energy in Borneo: comparing fluxes over oil palm plantations and a rainforest.

This paper reports measurements of land-atmosphere fluxes of sensible and latent heat, momentum, CO(2), volatile organic compounds (VOCs), NO, NO(2), N(2)O and O(3) over a 30 m high rainforest canopy and a 12 m high oil palm plantation in the same region of Sabah in Borneo between April and July 2008. The daytime maximum CO(2) flux to the two canopies differs by approximately a factor of 2, 1200 mg C m(-2) h(-1) for the oil palm and 700 mg C m(-2) h(-1) for the rainforest, with the oil palm plantation showing a substantially greater quantum efficiency. Total VOC emissions are also larger over the oil palm than over the rainforest by a factor of 3. Emissions of isoprene from the oil palm canopy represented 80 per cent of the VOC emissions and exceeded those over the rainforest in similar light and temperature conditions by on average a factor of 5. Substantial emissions of estragole (1-allyl-4-methoxybenzene) from the oil palm plantation were detected and no trace of this VOC was detected in or above the rainforest. Deposition velocities for O(3) to the rainforest were a factor of 2 larger than over oil palm. Emissions of nitrous oxide were larger from the soils of the oil palm plantation than from the soils of the rainforest by approximately 25 per cent. It is clear from the measurements that the large change in the species composition generated by replacing rainforest with oil palm leads to profound changes in the net exchange of most of the trace gases measured, and thus on the chemical composition of the boundary layer over these surfaces.