An extensive set of in situ water vapor (H 2 O) data obtained by the IAGOS-CARIBIC passenger aircraft at 10-12 km altitude over 8 years (2005)(2006)(2007)(2008)(2009)(2010)(2011)(2012)(2013) is analyzed. A multifaceted description of the vertical distribution of H 2 O from the upper troposphere (UT) via the extratropical tropopause mixing layer (exTL) into the lowermost stratosphere (LMS) is given. Compared to longer-lived trace gases, H 2 O is highly variable in the UT and exTL. It undergoes considerable seasonal variation, with maxima in summer and in phase from the UT up to~4 km above the tropopause. The transport and dehydration pathways of air starting at the Earth's surface and ending at 10-12 km altitude are reconstructed based upon (i) potential temperature (θ), (ii) relative humidity with respect to ice (RHi), and (iii) back trajectories as a function of altitude relative to the tropopause. RHi of an air mass was found to be primarily determined by its temperature change during recent vertical movement, i.e., cooling during ascent/expansion and warming during descent/compression. The data show, with great clarity, that H 2 O and RHi at 10-12 km altitude are controlled by three dominant transport/dehydration pathways: (i) the Hadley circulation, i.e., convective uplift in the tropics and poleward directed subsidence drying from the tropical tropopause layer with observed RHi down to 2%; (ii) warm conveyor belts and midlatitude convection transporting moist air into the UT with observed RHi usually above 60%; and (iii) the Brewer-Dobson shallow and deep branches with observed RHi down to 1%.
Abstract. Goal of the project CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrumented Container) is to carry out regular and detailed observations of atmospheric composition (particles and gases) at cruising altitudes of passenger aircraft, i.e. at 9-12 km. Mercury has been measured since May 2005 by a modified Tekran instrument (Tekran Model 2537 A analyser, Tekran Inc., Toronto, Canada) during monthly intercontinental flights between Europe and South and North America, Africa, and Asia. Here we describe the instrument modifications, the post-flight processing of the raw instrument signal, and the fractionation experiments.
Abstract. The ash cloud of the Eyjafjallajökull (also referred to as: Eyjafjalla (e.g. Schumann et al., 2011), Eyjafjöll or Eyjafjoll (e.g. Ansmann et al., 2010)) volcano on Iceland caused closure of large parts of European airspace in April and May 2010. For the validation and improvement of the European volcanic ash forecast models several research flights were performed. Also the CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container) flying laboratory, which routinely measures at cruise altitude (≈11 km) performed three dedicated measurements flights through sections of the ash plume. Although the focus of these flights was on the detection and quantification of the volcanic ash, we report here on sulphur dioxide (SO 2 ) and bromine monoxide (BrO) measurements with the CARIBIC DOAS (Differential Optical Absorption Spectroscopy) instrument during the second of these special flights on 16 May 2010. As the BrO and the SO 2 observations coincide, we assume the BrO to have been formed inside the volcanic plume. Average SO 2 and BrO mixing ratios of ≈40 ppb and ≈5 ppt respectively are retrieved inside the plume. The BrO to SO 2 ratio retrieved from the CARIBIC observation is ≈1.3×10 −4 . Both SO 2 and BrO observations agree well with simultaneous satellite (GOME-2) observations. SO 2 column densities retrieved from satellite observations are often used as an indicator for volcanic ash. As the CARIBIC O 4 column densities changed rapidly during the Correspondence to: K.-P. Heue (klaus-peter.heue@mpic.de) plume observation, we conclude that the aerosol and the SO 2 plume are collocated. For SO 2 some additional information on the local distribution can be derived from a comparison of forward and back scan GOME-2 data. More details on the local plume size and position are retrieved by combining CARIBIC and GOME-2 data.
During the summer monsoon the upper troposphere over South Asia is characterized by the monsoon anticyclone centered above the Tibetan Plateau. Surface air that has been rapidly transported upwards through deep convection becomes trapped within the strong anticyclonic circulation. Observations of trace gases within this anticyclone by the CARIBIC flying observatory revealed large enhancements in the greenhouse gas methane (CH4), which increased over the course of the monsoon. Meteorological analysis indicated that these air masses originated primarily in India, for which relatively little is known about CH4 emissions. Using correlations between concentrations of CH4 and carbon monoxide (CO) we estimated total emissions of 30.8 Tg CH4during the 2008 monsoon season (June–September), 19.7 Tg of which were identified as additional, monsoon‐related biogenic methane using the relationship of CH4 to ethane (C2H6). After accounting for the ∼3.9 Tg attributed to rice agriculture in the current inventories, ∼15.8 Tg of additional CH4 remain. Underestimated rice emissions provide a partial explanation, with the remainder most likely attributable to microbial production in waterlogged areas such as landfills, polluted waterways and wetlands.
Tropospheric sections of flights with the CARIBIC (Civil Aircraft for Regular Investigation of the Atmosphere Based on an Instrumented Container) observatory from May 2005 until June 2013, are investigated for the occurrence of plumes with elevated Hg concentrations. Additional information on CO, CO 2 , CH 4 , NOy, O 3 , hydrocarbons, halocarbons, acetone and acetonitrile enable us to attribute the plumes to biomass burning, urban/industrial sources or a mixture of both. Altogether, 98 pollution plumes with elevated Hg concentrations and CO mixing ratios were encountered, and the Hg/CO emission ratios for 49 of them could be calculated. Most of the plumes were found over East Asia, in the African equatorial region, over South America and over Pakistan and India. The plumes encountered over equatorial Africa and over South America originate predominantly from biomass burning, as evidenced by the low Hg/CO emission ratios and elevated mixing ratios of acetonitrile, CH 3 Cl and particle concentrations. The backward trajectories point to the regions around the Rift Valley and the Amazon Basin, with its outskirts, as the source areas. The plumes encountered over East Asia and over Pakistan and India are predominantly of urban/industrial origin, sometimes mixed with products of biomass/biofuel burning. Backward trajectories point mostly to source areas in China and northern India. The Hg/CO 2 and Hg/CH 4 emission ratios for several plumes are also presented and discussed.
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