Publications by authors named "Hartwig Harder"

Aircraft observations have revealed ubiquitous new particle formation in the tropical upper troposphere over the Amazon and the Atlantic and Pacific oceans. Although the vapours involved remain unknown, recent satellite observations have revealed surprisingly high night-time isoprene mixing ratios of up to 1 part per billion by volume (ppbv) in the tropical upper troposphere. Here, in experiments performed with the CERN CLOUD (Cosmics Leaving Outdoor Droplets) chamber, we report new particle formation initiated by the reaction of hydroxyl radicals with isoprene at upper-tropospheric temperatures of -30 °C and -50 °C.

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New particle formation (NPF) in the tropical upper troposphere is a globally important source of atmospheric aerosols. It is known to occur over the Amazon basin, but the nucleation mechanism and chemical precursors have yet to be identified. Here we present comprehensive in situ aircraft measurements showing that extremely low-volatile oxidation products of isoprene, particularly certain organonitrates, drive NPF in the Amazonian upper troposphere.

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Article Synopsis
  • Ammonia emissions in Southeast Asia significantly impact air pollution and the development of the Asian Tropopause Aerosol Layer (ATAL), particularly during summer when the South Asian monsoon is active.
  • The study utilizes the EMAC chemistry-climate model to analyze how ammonia influences particle formation, revealing a tenfold increase in particle creation during the day, especially within the monsoon's upper troposphere and lower stratosphere (UTLS).
  • Findings indicate that while ammonia enhances cloud condensation nuclei (CCN) concentrations and aerosol optical depth (AOD), its effect on aerosol mass in the ATAL is comparatively limited, suggesting a complex relationship between ammonia, particle growth, and aerosol composition.
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Forest emissions of biogenic volatile organic compounds (BVOCs), such as isoprene and other terpenes, play a role in the production of tropospheric ozone and aerosols. In a northern Michigan forest, the direct measurement of total OH reactivity, which is the inverse of the OH lifetime, was significantly greater than expected. The difference between measured and expected OH reactivity, called the missing OH reactivity, increased with temperature, as did emission rates for terpenes and other BVOCs.

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