Abstract

Abstract. The chemistry in large thunderstorm clouds is influenced by local lightning-NOx production and uplift of boundary layer air. Under these circumstances trace gases like nitrous acid (HONO) or formaldehyde (HCHO) are expected to be formed or to reach the tropopause region. However, up to now only few observations of HONO at this altitude have been reported. Here we report on a case study where enhancements in HONO, HCHO and nitrogen oxides (NOx) were observed by the CARIBIC flying laboratory (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container). The event took place in a convective system over the Caribbean Sea in August 2011. Inside the cloud the light path reaches up to 100 km. Therefore the DOAS instrument on CARIBIC was very sensitive to the tracers inside the cloud. Based on the enhanced slant column densities of HONO, HCHO and NO2, average mixing ratios of 37, 468 and 210 ppt, respectively, were calculated. These data represent averages for constant mixing ratios inside the cloud. However, a large dependency on the assumed profile is found; for HONO a mixing ratio of 160 ppt is retrieved if the total amount is assumed to be situated in the uppermost 2 km of the cloud. The NO in situ instrument measured peaks up to 5 ppb NO inside the cloud; the background in the cloud was about 1.3 ppb, and hence clearly above the average outside the cloud (≈ 150 ppt). The high variability and the fact that the enhancements were observed over a pristine marine area led to the conclusion that, in all likelihood, the high NO concentrations were caused by lighting. This assumption is supported by the number of flashes that the World Wide Lightning Location Network (WWLLN) counted in this area before and during the overpass. The chemical box model CAABA is used to estimate the NO and HCHO source strengths which are necessary to explain our measurements. For NO a source strength of 10 × 109 molec cm−2 s−1 km−1 is found, which corresponds to the lightning activity as observed by the World Wide Lightning Location network, and lightning emissions of 5 × 1025 NO molec flash−1 (2.3–6.4 × 1025). The uncertainties are determined by a change of the input parameters in the box model, the cloud top height and the flash density. The emission rate per flash is scaled up to a global scale and 1.9 (1.4–2.5) tg N a−1 is estimated. The HCHO updraught is of the order of 120 × 109 molec cm−2 s−1 km−1. Also isoprene and CH3OOH as possible HCHO sources are discussed.

Highlights

  • Nitrous acid (HONO) and especially its relevance for OH production and photochemistry has been studied for many years (Platt et al, 1980)

  • We focus on the centre of the cloud, it is interesting to mention that this slight increase might be caused by quite high HONO concentration inside and above the cloud top

  • The differential optical absorption spectroscopy (DOAS) instrument is less sensitive for trace gases at lower altitudes, if most of the NO2 is below 6 km, the same slant column density can only be explained by much higher concentrations i.e. 580 ppt below 6 km followed by the exponential decrease

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Summary

Introduction

Nitrous acid (HONO) and especially its relevance for OH production and photochemistry has been studied for many years (Platt et al, 1980). In cloud tops the solar radiation is enhanced by up to a factor of 3 (2–5 Brasseur et al, 2002) and the photolysis frequency JR7 increases and the Leighton ratio reaches up to 30 Under these conditions OH radicals have a low probability of being removed, which leads to a large HONO formation rate on top of high-reaching thunderstorm clouds. In this study we present CARIBIC DOAS observations of HONO, NO2 and HCHO inside a large cloud system of about 480 km length over the Caribbean islands of Guadeloupe To our knowledge, this is only the second publication about nitrous acid in a deep convective cloud, after Dix et al (2009). Due to the high column densities inside the cloud, and the enhancement in HCHO and NOx we will focus on this special event here

The CARIBIC instruments and the CAABA box model
Water measurements
Nitrogen oxides measurements
DOAS on CARIBIC
CAABA box model
Observations
Background
Light path estimates
Trace gas concentrations in the cloud
Error estimates
Nitrogen oxides
Nitrous acid and OH
Formaldehyde
Updraught from the boundary layer
Oxidation of methane and other hydrocarbons
Altitude effects
CAABA box model simulations
Estimates of the lightning emission factor
Conclusions
Light path estimate
Full Text
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