The aim of the study is to propose a technique for the retrieval of point sources of atmospheric trace species from concentration measurements. The inverse problem of identifying the parameters of a point source is addressed within the assimilative framework of renormalization recently proposed for the identification of distributed emissions. This theory has been extended for the point sources based on the property that these are associated with the maximum of the renormalized estimate computed from the observations. This approach along with an analytic dispersion model is used for point source identification, and the sensitivity of the samplers is described by the same model in backward mode. The proposed technique is illustrated not only with synthetic measurements but also with seven sets of observations, corresponding to convective conditions, taken from the lowwind tracer diffusion experiment conducted at the Indian Institute of Technology Delhi in 1991. The position and intensity of the source are retrieved exactly with the synthetic measurements in all the sets validating the technique. The position of the source is retrieved with an average error of 17 m, mostly along wind; its intensity is estimated within a factor 2 for all the sets of real observations. From a theoretical point of view, the link established between point and distributed sources clarifies new concepts for the exploitation of monitoring networks. In particular, the influence of the noise on the identification of a source is related to the relative visibility of the various regions described with a renormalizing weight function. The geometry of the environment modified according to the weights is interpreted as an apparent geometry. It is analogous to the apparent flatness of the starry sky in eye's view, usually considered an impression rather than a scientific fact.

Abstract. We present a local-scale atmospheric inversion framework to estimate the location and rate of methane (CH4) and carbon dioxide (CO2) releases from point sources. It relies on mobile near-ground atmospheric CH4 and CO2 mole fraction measurements across the corresponding atmospheric plumes downwind of these sources, on high-frequency meteorological measurements, and on a Gaussian plume dispersion model. The framework exploits the scatter of the positions of the individual plume cross sections, the integrals of the gas mole fractions above the background within these plume cross sections, and the variations of these integrals from one cross section to the other to infer the position and rate of the releases. It has been developed and applied to provide estimates of brief controlled CH4 and CO2 point source releases during a 1-week campaign in October 2018 at the TOTAL experimental platform TADI in Lacq, France. These releases typically lasted 4 to 8 min and covered a wide range of rates (0.3 to 200 g CH4/s and 0.2 to 150 g CO2/s) to test the capability of atmospheric monitoring systems to react fast to emergency situations in industrial facilities. It also allowed testing of their capability to provide precise emission estimates for the application of climate change mitigation strategies. However, the low and highly varying wind conditions during the releases added difficulties to the challenge of characterizing the atmospheric transport over the very short duration of the releases. We present our series of CH4 and CO2 mole fraction measurements using instruments on board a car that drove along roads ∼50 to 150 m downwind of the 40 m × 60 m area for controlled releases along with the estimates of the release locations and rates. The comparisons of these results to the actual position and rate of the controlled releases indicate ∼10 %–40 % average errors (depending on the inversion configuration or on the series of tests) in the estimates of the release rates and ∼30–40 m errors in the estimates of the release locations. These results are shown to be promising, especially since better results could be expected for longer releases and under meteorological conditions more favorable to local-scale dispersion modeling. However, the analysis also highlights the need for methodological improvements to increase the skill for estimating the source locations.

Abstract. We present a local-scale atmospheric inversion framework to estimate the location and rate of methane (CH4) and carbon dioxide (CO2) releases from point sources. It relies on mobile near-ground atmospheric CH4 and CO2 mole fraction measurements across the corresponding atmospheric plumes downwind the sources, on high-frequency meteorological measurements, and a Gaussian plume dispersion model. It exploits the spread of the positions of individual plume cross-sections and the integrals of the gas mole fractions above the background within these plume cross-sections to infer the position and rate of the releases. It has been developed and applied to provide estimates of brief controlled CH4 and CO2 point source releases during a one-week campaign in October 2018 at the TOTAL's experimental platform TADI in Lacq, France. These releases lasted typically 4 to 8 minutes and covered a wide range of rates (0.3 to 200 gCH4/s and 0.2 to 150 gCO2/s) to test the capability of atmospheric monitoring systems to react fast to emergency situations in industrial facilities. It also allowed testing their capability to provide precise emission estimates for the application of climate change mitigation strategies. However, the low and highly varying wind conditions during the releases added difficulties to the challenge of characterizing the atmospheric transport over the very short duration of the releases. We present our series of measurements of CH4 and CO2 mole fractions using instruments onboard a car that drives along the roads ~50 to 150 m downwind the 40 m × 60 m area of controlled releases for each of the releases and the results from the inversions of the release locations and rates. The comparisons of these results to the actual position and rate of the controlled release indicate a 20 %–30 % average error on the release rates and a ~30–40 m errors in the estimates of the release locations. These results are shown to be promising especially since better results could be expected for longer releases and under meteorological conditions more favorable to local scale dispersion modeling.

For the dispersion of a pollutant released from a continuous source in the atmospheric boundary layer (ABL), a generalized analytical model describing the crosswind-integrated concentrations is presented. An analytical scheme is described to solve the resulting twodimensional steady-state advection-diffusion equation for horizontal wind speed as a generalized function of vertical height above the ground and eddy diffusivity as a function of both downwind distance from the source and vertical height. Special cases of this model are deduced and an extensive analysis is carried out to compare the model with the known analytical models by taking the particular forms of wind speed and vertical eddy diffusivity.The proposed model is evaluated with the observations obtained from Copenhagen diffusion experiments in unstable conditions and Hanford and Prairie Grass experiments in stable conditions. In evaluation of the model, a recently proposed formulation for the wind speed in the entire ABL is used. It is concluded that the present model is performing well with the observations and can be used to predict the short-range dispersion from a continuous release. Further, it is shown that the accurate parameterizations of wind speed and eddy diffusivity provide a significant improvement in the agreement between computed and observed concentrations.