This paper describes process-based estimation of CH4 emissions from sources in Indianapolis, IN and compares these with atmospheric inferences of whole city emissions. Emissions from the natural gas distribution system were estimated from measurements at metering and regulating stations and from pipeline leaks. Tracer methods and inverse plume modeling were used to estimate emissions from the major landfill and wastewater treatment plant. These direct source measurements informed the compilation of a methane emission inventory for the city equal to 29 Gg/yr (5% to 95% confidence limits, 15 to 54 Gg/yr). Emission estimates for the whole city based on an aircraft mass balance method and from inverse modeling of CH4 tower observations were 41 ± 12 Gg/yr and 81 ± 11 Gg/yr, respectively. Footprint modeling using 11 days of ethane/methane tower data indicated that landfills, wastewater treatment, wetlands, and other biological sources contribute 48% while natural gas usage and other fossil fuel sources contribute 52% of the city total. With the biogenic CH4 emissions omitted, the top-down estimates are 3.5-6.9 times the nonbiogenic city inventory. Mobile mapping of CH4 concentrations showed low level enhancement of CH4 throughout the city reflecting diffuse natural gas leakage and downstream usage as possible sources for the missing residual in the inventory.

We report the CH 4 emission flux from the city of Indianapolis, IN, the site of the Indianapolis Flux Experiment (INFLUX) project for developing, assessing, and improving top-down and bottom-up approaches for quantifying urban greenhouse gas emissions. Using an aircraft-based mass balance approach, we find that the average CH 4 emission rate from five flight experiments in 2011 is 135 ± 58 (1σ) moles s-1 (7800 ± 3300 kg hr-1). The effective per capita CH 4 emission rate for Indianapolis is 77 kg CH 4 person-1 yr-1 , a figure that is less than the national anthropogenic CH 4 emission (∼91 kg CH 4 person-1 yr-1) but considerably larger than the global figure (∼48 kg CH 4 person-1 yr-1). We consistently observed elevated CH 4 concentrations at specific coordinates along our flight transects downwind of the city. Inflight investigations as well as back trajectories using measured wind directions showed that the elevated concentrations originated from the southwest side of the city where a landfill and a natural gas transmission regulating station (TRS) are located. Street level mobile measurements downwind of the landfill and the TRS supported the results of aircraft-based data, and were used to quantify the relative contributions from the two sources. We find that the CH 4 emission from the TRS was negligible relative to the landfill, which was responsible for 33 ± 10% of the citywide emission flux. A regression of propane versus methane from aircraft flask samples suggests that the remaining citywide CH 4 emissions (∼67%) derive from the natural gas distribution system. We discuss the combination of surface mobile observations and aircraft city-wide flux measurements to determine the total flux and apportionment to important sources.

To effectively address climate change, aggressive mitigation policies need to be implemented to reduce greenhouse gas emissions. Anthropogenic carbon emissions are mostly generated from urban environments, where human activities are spatially concentrated. Improvements in uncertainty determinations and precision of measurement techniques are critical to permit accurate and precise tracking of emissions changes relative to the reduction targets. As part of the INFLUX project, we quantified carbon dioxide (CO2), carbon monoxide (CO) and methane (CH4) emission rates for the city of Indianapolis by averaging results from nine aircraft-based mass balance experiments performed in November-December 2014. Our goal was to assess the achievable precision of the aircraft-based mass balance method through averaging, assuming constant CO2, CH4 and CO emissions during a three-week field campaign in late fall. The averaging method leads to an emission rate of 14,600 mol/s for CO2, assumed to be largely fossil-derived for this period of the year, and 108 mol/s for CO. The relative standard error of the mean is 17% and 16%, for CO2 and CO, respectively, at the 95% confidence level (CL), i.e. a more than 2-fold improvement from the previous estimate of ~40% for single-flight measurements for Indianapolis. For CH4, the averaged emission rate is 67 mol/s, while the standard error of the mean at 95% CL is large, i.e. ±60%. Given the results for CO2 and CO for the same flight data, we conclude that this much larger scatter in the observed CH4 emission rate is most likely due to variability of CH4 emissions, suggesting that the assumption of constant daily emissions is not correct for CH4 sources. This work shows that repeated measurements using aircraft-based mass balance methods can yield sufficient precision of the mean to inform emissions reduction efforts by detecting changes over time in urban emissions.

Urban areas are responsible for a substantial fraction of anthropogenic emissions of greenhouse gases (GHGs) including methane (CH4), with the second largest anthropogenic direct radiative forcing relative to carbon dioxide (CO2). Quantification of urban CH4 emissions is important for establishing GHG mitigation policies. Comparison of observation‐based and inventory‐based urban CH4 emissions suggests possible improvements in estimating CH4 source emissions in urban environments. In this study, we quantify CH4 emissions from the Baltimore‐Washington area based on the mass balance aircraft flight experiments conducted in Winters 2015 and 2016. The field measurement‐based mean winter CH4 emission rates from this area were 8.66 ± 4.17 kg/s in 2015 and 9.14 ± 4.49 kg/s in 2016, which are 2.8 times the 2012 average U.S. GHG Inventory‐based emission rate. The observed emission rate is 1.7 times that given in a population‐apportioned state of Maryland inventory. Methane emission rates inferred from carbon monoxide (CO) and CO2 emission inventories and observed CH4/CO and CH4/CO2 enhancement ratios are similar to those from the mass balance approach. The observed ethane‐to‐methane ratios, with a mean value of 3.3% in Winter 2015 and 4.3% in Winter 2016, indicate that the urban natural gas system could be responsible for ~40–60% of total CH4 emissions from this area. Landfills also appear to be a major contributor, providing 25 ± 15% of the total emissions for the region. Our study suggests there are grounds to reexamine the CH4 emissions estimates for the Baltimore‐Washington area and to conduct flights in other seasons.

A Halo Photonics Stream Line XR Doppler lidar has been deployed for the Indianapolis Flux Experiment (INFLUX) to measure profiles of the mean horizontal wind and the mixing layer height for quantification of greenhouse gas emissions from the urban area. To measure the mixing layer height continuously and autonomously, a novel composite fuzzy logic approach has been developed that combines information from various scan types, including conical and vertical-slice scans and zenith stares, to determine a unified measurement of the mixing height and its uncertainty. The composite approach uses the strengths of each measurement strategy to overcome the limitations of others so that a complete representation of turbulent mixing is made in the lowest km, depending on clouds and aerosol distribution. Additionally, submeso nonturbulent motions are identified from zenith stares and removed from the analysis, as these motions can lead to an overestimate of the mixing height. The mixing height is compared with in situ profile measurements from a research aircraft for validation. To demonstrate the utility of the measurements, statistics of the mixing height and its diurnal and annual variability for 2016 are also presented. The annual cycle is clearly captured, with the largest and smallest afternoon mixing heights observed at the summer and winter solstices, respectively. The diurnal cycle of the mixing layer is affected by the mean wind, growing slower in the morning and decaying more rapidly in the evening with lighter winds.