[1] The ice nucleating efficiency of many important atmospheric particles remains poorly understood. Here we investigate the ice nucleation properties of a range of soot types including soot that has been treated with atmospherically relevant amounts of ozone. We focus on deposition nucleation below water saturation and at temperatures ranging from 243 to 258 K. For our experimental conditions, ice nucleation never occurred at temperatures above 248 K and below water saturation. Below 248 K, ice occasionally formed in our experiments with no indication of the formation of water droplets prior to ice formation. However, even at these temperatures the relative humidity with respect to ice (RH i ) was close to water saturation when ice nucleation was observed, suggesting water nucleation may have occurred first followed by ice nucleation during the condensation process. We also performed a complimentary set of experiments where we held soot particles at 248 K and RH i = 124 ± 4%, which is just below water saturation, for a period of 8 hours. From these measurements we calculated an upper limit of the heterogeneous ice nucleation rate coefficient of 0.1 cm À2 s
À1. If the number of soot particles is 1.5 Â 10 5 L À1 in the atmosphere (which corresponds to urban-influenced rural areas), then the number of ice particles produced below water saturation at these conditions is at most 0.1 particles L À1 on the basis of our upper limit. We conclude from our studies that deposition nucleation of ice on most types of soot particles is not important in the Earth's troposphere above 243 K and below water saturation.
The Permian Basin is the largest and fastest growing oil and gas (O&G) producing region in the United States. We conducted an extensive airborne campaign across the majority of the Permian in September−November, 2019 with imaging spectrometers to quantify strong methane (CH 4 ) point source emissions at facility-scales, including high frequency sampling to evaluate intermittency. We identified 1100 unique and heavy-tailed distributed sources that were sampled at least 3 times (average 8 times), showing 26% average persistence. Sources that were routinely persistent (50−100%) make up only 11% of high emitting infrastructure but 29% of quantified emissions from this population, potentially indicative of leaking equipment that merits repair. Sector attribution of plumes shows that 50% of detected emissions result from O&G production, 38% from gathering and boosting, and 12% from processing. This suggests a 20% relative shift from upstream to midstream compared to other US O&G basins for large emitters. Simultaneous spectroscopic identification of flares found that 12% of detected Permian CH 4 plume emissions were associated with either active or inactive flares. Frequent, high-resolution monitoring is necessary to accurately understand intermittent methane superemitters across large, heterogeneous O&G basins and efficiently pinpoint persistent leaks for mitigation.
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