Measurements of Methane Emissions from a Biofertilizer Storage Tank Using Ground-Based Hyperspectral Imaging and Flux Chambers.

Open storages of organic material represent potentially large sources of the greenhouse gas methane (CH4), an emissions source that will likely become more common as a part of societal efforts toward sustainability. Hence, monitoring and minimizing CH4 emissions from such facilities are key, but effective assessment of emissions without disturbing the flux is challenging. We demonstrate the capacity of using a novel high-resolution hyperspectral camera to perform sensitive CH4 flux assessments at such facilities, using as a test case a biofertilizer storage tank for residual material from a biogas plant. The camera and simultaneous conventional flux chamber measurements showed emissions of 6.0 ± 1.3 and 13 ± 5.7 kg of CH4 h-1, respectively. The camera measurements covered the whole tank surface of 1104 m2, and the chamber results were extrapolated from measurements over 5 m2. This corresponds to 0.7-1.4% of the total CH4 production at the biogas plant (1330 N m3 h-1 corresponding to 950 kg h-1). The camera could assess the entire tank emission in minutes without disturbing normal operations at the plant and revealed additional unknown emissions from the inlet to the tank (17 g of CH4 h-1) and during the loading of the biofertilizer into trucks (3.1 kg of CH4 h-1 during loading events). This study illustrates the importance of adequate measurement capacity to map methane fluxes and to verify that methane emission mitigation efforts are effective. Given the high methane emissions observed, it is important to reduce methane emissions from open storage of organic material, for example by improved digestion in the biogas reactor, precooling of sludge before storage, or building gastight storage tanks with sealed covers. We conclude that hyperspectral, ground-based remote sensing is a promising approach for greenhouse gas monitoring and mitigation.

Higher Apparent Gas Transfer Velocities for CO2 Compared to CH4 in Small Lakes.

Large greenhouse gas emissions occur via the release of carbon dioxide (CO2) and methane (CH4) from the surface layer of lakes. Such emissions are modeled from the air-water gas concentration gradient and the gas transfer velocity (k). The links between k and the physical properties of the gas and water have led to the development of methods to convert k between gases through Schmidt number normalization. However, recent observations have found that such normalization of apparent k estimates from field measurements can yield different results for CH4 and CO2. We estimated k for CO2 and CH4 from measurements of concentration gradients and fluxes in four contrasting lakes and found consistently higher (on an average 1.7 times) normalized apparent k values for CO2 than CH4. From these results, we infer that several gas-specific factors, including chemical and biological processes within the water surface microlayer, can influence apparent k estimates. We highlight the importance of accurately measuring relevant air-water gas concentration gradients and considering gas-specific processes when estimating k.

Ground-based remote sensing of CH4 and N2O fluxes from a wastewater treatment plant and nearby biogas production with discoveries of unexpected sources.

This study is an attempt to assess CH4 and N2O emissions from all the treatment steps of a wastewater treatment plant (WWTP) in Sweden, serving 145 000 persons, and an adjacent biogas production facility. We have used novel mid-IR ground-based remote sensing with a hyperspectral camera to visualize and quantify the emissions on 21 days during a year, with resulting yearly fluxes of 90.4 ± 4.3 tonne CH4/yr and 10.9 ± 1.3 tonne N2O/yr for the entire plant. The most highly emitting CH4 source was found to be sludge storage, which is seldom included in literature as in-situ methods are not suitable for measuring emissions extended over large surfaces, still contributing 90 % to the total CH4 emission in our case. The dominating N2O source was found to be a Stable High rate Ammonia Removal Over Nitrite reactor, contributing 89 % to the total N2O emissions. We also discovered several unexpected CH4 sources. Incomplete flaring of CH4 gave fluxes of at least 30 kg CH4/min, corresponding to plume concentrations of 2.5 %. Such highly episodic fluxes could double the plant-wide yearly emissions if they occur 2 days per year. From a distance of 250 m we found a leak in the biogas production facility, corresponding to 1.1 % of the CH4 produced, and that loading of organic material onto trucks from a biofertilizer storage tank contributed with high emissions during loading events. These results indicate that WWTP emissions globally may have been grossly underestimated and that it is essential to have effective methods that can measure all types of fluxes, and discover new potential sources, in order to make adequate priorities and to take effective actions to mitigate greenhouse gas emissions from WWTPs.

Sensitive Drone Mapping of Methane Emissions without the Need for Supplementary Ground-Based Measurements.

Methane (CH4) is one of the main greenhouse gas for which sources and sinks are poorly constrained and better capacity of mapping landscape emissions are broadly requested. A key challenge has been comprehensive, accurate, and sensitive emission measurements covering large areas at a resolution that allows separation of different types of local sources. We present a sensitive drone-based system for mapping CH4 hotspots, finding leaks from gas systems, and calculating total CH4 fluxes from anthropogenic environments such as wastewater treatment plants, landfills, energy production, biogas plants, and agriculture. All measurements are made on-board the drone, with no requirements for additional ground-based instruments. Horizontal flight patterns are used to map and find emission sources over large areas and vertical flight patterns for total CH4 fluxes using mass balance calculations. The small drone system (6.7 kg including batteries, sensors, loggers, and weather proofing) maps CH4 concentrations and wind speeds at 1 Hz with a precision of 0.84 ppb/s and 0.1 m/s, respectively. As a demonstration of the system and the mass balance method for a CH4 source that is difficult to assess with traditional methods, we have quantified fluxes from a sludge deposit at a wastewater treatment plant. Combining data from three 10 min flights, emission hotspots could be mapped and a total flux of 178.4 ± 8.1 kg CH4 d-1 was determined.

Turbulence in a small boreal lake: Consequences for air-water gas exchange.

The hydrodynamics within small boreal lakes have rarely been studied, yet knowing whether turbulence at the air-water interface and in the water column scales with metrics developed elsewhere is essential for computing metabolism and fluxes of climate-forcing trace gases. We instrumented a humic, 4.7 ha, boreal lake with two meteorological stations, three thermistor arrays, an infrared (IR) camera to quantify surface divergence, obtained turbulence as dissipation rate of turbulent kinetic energy (ε) using an acoustic Doppler velocimeter and a temperature-gradient microstructure profiler, and conducted chamber measurements for short periods to obtain fluxes and gas transfer velocities (k). Near-surface ε varied from 10-8 to 10-6 m2 s-3 for the 0-4 m s-1 winds and followed predictions from Monin-Obukhov similarity theory. The coefficient of eddy diffusivity in the mixed layer was up to 10-3 m2 s-1 on the windiest afternoons, an order of magnitude less other afternoons, and near molecular at deeper depths. The upper thermocline upwelled when Lake numbers (L N ) dropped below four facilitating vertical and horizontal exchange. k computed from a surface renewal model using ε agreed with values from chambers and surface divergence and increased linearly with wind speed. Diurnal thermoclines formed on sunny days when winds were < 3 m s-1, a condition that can lead to elevated near-surface ε and k. Results extend scaling approaches developed in the laboratory and for larger water bodies, illustrate turbulence and k are greater than expected in small wind-sheltered lakes, and provide new equations to quantify fluxes.

Remote sensing of methane and nitrous oxide fluxes from waste incineration.

Incomplete combustion processes lead to the formation of many gaseous byproducts that can be challenging to monitor in flue gas released via chimneys. This study presents ground-based remote sensing approaches to make greenhouse gas (GHG) flux measurements of methane (CH4) and nitrous oxide (N2O) from a waste incineration chimney at distances of 150-200 m. The study found emission of N2O (corresponding to 30-40 t yr-1), which is a consequence of adding the reduction agent urea to decrease NOX emissions due to NOX regulation; a procedure that instead increases N2O emissions (which is approximately 300 times more potent as a GHG than CO2 on a 100-year time scale). CH4 emissions of 7-11 t yr-1 was also detected from the studied chimney despite the usage of a high incineration temperature. For this particular plant, local knowledge is high and emission estimates at corresponding levels have been reported previously. However, emissions of CH4 are often not included in GHG emission inventories for waste incineration. This study highlights the importance of monitoring combustion processes, and shows the possibility of surveying CH4 and N2O emissions from waste incineration at distances of several hundred meters.