Abstract. Atmospheric new particle formation (NPF) is an important phenomenon in terms of global particle number concentrations. Here we investigated the frequency of NPF, formation rates of 10 nm particles, and growth rates in the size range of 10–25 nm using at least 1 year of aerosol number size-distribution observations at 36 different locations around the world. The majority of these measurement sites are in the Northern Hemisphere. We found that the NPF frequency has a strong seasonal variability. At the measurement sites analyzed in this study, NPF occurs most frequently in March–May (on about 30 % of the days) and least frequently in December–February (about 10 % of the days). The median formation rate of 10 nm particles varies by about 3 orders of magnitude (0.01–10 cm−3 s−1) and the growth rate by about an order of magnitude (1–10 nm h−1). The smallest values of both formation and growth rates were observed at polar sites and the largest ones in urban environments or anthropogenically influenced rural sites. The correlation between the NPF event frequency and the particle formation and growth rate was at best moderate among the different measurement sites, as well as among the sites belonging to a certain environmental regime. For a better understanding of atmospheric NPF and its regional importance, we would need more observational data from different urban areas in practically all parts of the world, from additional remote and rural locations in North America, Asia, and most of the Southern Hemisphere (especially Australia), from polar areas, and from at least a few locations over the oceans.
Abstract. We present airborne measurements of carbon dioxide (CO 2 ), carbon monoxide (CO), ozone (O 3 ), equivalent black carbon (EBC) and ultra fine particles over NorthEastern Siberia in July 2008 performed during the YAK-AEROSIB/POLARCAT experiment. During a "golden day" (11 July 2008) a number of biomass burning plumes were encountered with CO mixing ratio enhancements of up to 500 ppb relative to a background of 90 ppb. Number concentrations of aerosols in the size range 3.5-200 nm peaked at 4000 cm −3 and the EBC content reached 1.4 µg m −3 . These high concentrations were caused by forest fires in the vicinity of the landing airport in Yakutsk where measurements in fresh smoke could be made during the descent. We estimate a combustion efficiency of 90 ± 3% based on CO and CO 2 measurements and a CO emission factor of 65.5±10.8 g CO per kilogram of dry matter burned. This suggests a potential increase in the average northern hemispheric CO mixing ratio of 3.0-7.2 ppb per million hectares of Siberian forest burned. For BC, we estimate an emission factor of 0.52 ± 0.07 g BC kg −1 , comparable to values reported in the literature. The emission ratio of ultra-fine particles (3.5-200 nm) was 26 cm −3 (ppb CO) −1 , consistent with other airborne studies.The transport of identified biomass burning plumes was investigated using the FLEXPART Lagrangian model. Based on sampling of wildfire plumes from the same source but with different atmospheric ages derived from FLEXPART, Correspondence to: J.-D. Paris (jean-daniel.paris@lsce.ipsl.fr) we estimate that the e-folding lifetimes of EBC and ultra fine particles (between 3.5 and 200 nm in size) against removal and growth processes are 5.1 and 5.5 days respectively, supporting lifetime estimates used in various modelling studies.
Two airborne campaigns were carried out to measure the tropospheric concentrations and variability of CO2, CO and O3 over Siberia. In order to quantify the influence of remote and regional natural and anthropogenic sources, we analysed a total of 52 vertical profiles of these species collected in April and September 2006, every ∼200 km and up to 7 km altitude. CO2 and CO concentrations were high in April 2006 (respectively 385–390 ppm CO2 and 160–200 ppb CO) compared to background values. CO concentrations up to 220 ppb were recorded above 3.5 km over eastern Siberia, with enhancements in 500–1000 m thick layers. The presence of CO enriched air masses resulted from a quick frontal uplift of a polluted air mass exposed to northern China anthropogenic emissions and to fire emissions in northern Mongolia. A dominant Asian origin for CO above 4 km (71.0%) contrasted with a dominant European origin below this altitude (70.9%) was deduced both from a transport model analysis, and from the contrasted ΔCO/ΔCO2 ratio vertical distribution. In September 2006, a significant O3 depletion (∼–30 ppb) was repeatedly observed in the boundary layer, as diagnosed from virtual potential temperature profiles and CO2 gradients, compared to the free troposphere aloft, suggestive of a strong O3 deposition over Siberian forests.
also cannot be neglected. Daytime mean CH 4 concentrations from the Siberian tower sites were generally higher than CH 4 values reported at NOAA coastal sites in the same latitudinal zone, and the difference in concentrations between two sets of sites was reproduced with a coupled Eulerian-Lagrangian transport model. Simulations of emissions from different CH 4 sources suggested that the major contributor to variation switched from wetlands during summer to fossil fuel during winter.
[1] Being one of the largest carbon reservoirs in the world, the Siberian carbon sink however remains poorly understood due to the limited numbers of observation. We present the first results of atmospheric CO 2 inversions utilizing measurements from a Siberian tower network (Japan-Russia Siberian Tall Tower Inland Observation Network; JR-STATION) and four aircraft sites, in addition to surface background flask measurements by the National Oceanic and Atmospheric Administration (NOAA). Our inversion with only the NOAA data yielded a boreal Eurasian CO 2 flux of À0.56 AE 0.79 GtC yr À1 , whereas we obtained a weaker uptake of À0.35 AE 0.61 GtC yr À1when the Siberian data were also included. This difference is mainly explained by a weakened summer uptake, especially in East Siberia. We also found the inclusion of the Siberian data had significant impacts on inversion results over northeastern Europe as well as boreal Eurasia. The inversion with the Siberian data reduced the regional uncertainty by 22% on average in boreal Eurasia, and further uncertainty reductions up to 80% were found in eastern and western Siberia. Larger interannual variability was clearly seen in the inversion which includes the Siberia data than the inversion without the Siberia data.In the inversion with NOAA plus Siberia data, east Siberia showed a larger interannual variability than that in west and central Siberia. Finally, we conducted forward simulations using estimated fluxes and confirmed that the fit to independent measurements over central Siberia, which were not included in inversions, was greatly improved.Citation: Saeki, T., et al. (2013), Carbon flux estimation for Siberia by inverse modeling constrained by aircraft and tower CO 2 measurements,
Abstract. Eight surface observation sites providing quasicontinuous measurements of atmospheric methane mixing ratios have been operated since the mid-2000's in Siberia. For the first time in a single work, we assimilate 1 year of these in situ observations in an atmospheric inversion. Our objective is to quantify methane surface fluxes from anthropogenic and wetland sources at the mesoscale in the Siberian lowlands for the year 2010. To do so, we first inquire about the way the inversion uses the observations and the way the fluxes are constrained by the observation sites. As atmospheric inversions at the mesoscale suffer from mis-quantified sources of uncertainties, we follow recent innovations in inversion techniques and use a new inversion approach which quantifies the uncertainties more objectively than the previous inversion systems. We find that, due to errors in the representation of the atmospheric transport and redundant pieces of information, only one observation every few days is found valuable by the inversion. The remaining high-resolution quasicontinuous signal is representative of very local emission patterns difficult to analyse with a mesoscale system. An analysis of the use of information by the inversion also reveals that the observation sites constrain methane emissions within a radius of 500 km. More observation sites than the ones currently in operation are then necessary to constrain the whole Siberian lowlands. Still, the fluxes within the constrained areas are quantified with objectified uncertainties. Finally, the tolerance intervals for posterior methane fluxes are of roughly 20 % (resp. 50 %) of the fluxes for anthropogenic (resp. wetland) sources. About 50-70 % of Siberian lowlands emissions are constrained by the inversion on average on an annual basis. Extrapolating the figures on the constrained areas to the whole Siberian lowlands, we find a regional methane budget of 5-28 TgCH 4 for the year 2010, i.e. 1-5 % of the global methane emissions. As very few in situ observations are available in the region of interest, observations of methane total columns from the Greenhouse Gas Observing SATellite (GOSAT) are tentatively used for the evaluation of the inversion results, but they exhibit only a marginal signal from the fluxes within the region of interest.
Abstract. The northern Eurasian regions and Arctic Ocean will very likely undergo substantial changes during the next decades. The Arctic-boreal natural environments play a crucial role in the global climate via albedo change, carbon sources and sinks as well as atmospheric aerosol production from biogenic volatile organic compounds. Furthermore, it is expected that global trade activities, demographic movement, and use of natural resources will be increasing in the Arctic regions. There is a need for a novel research approach, which not only identifies and tackles the relevant multi-disciplinary research questions, but also is able to make a holistic system analysis of the expected feedbacks. In this paper, we introduce the research agenda of the Pan-Eurasian Experiment (PEEX), a multi-scale, multi-disciplinary and international program started in 2012 (https://www.atm.helsinki.fi/peex/). PEEX sets a research approach by which large-scale research topics are investigated from a system perspective and which aims to fill the key gaps in our understanding of the feedbacks and interactions between the land-atmosphereaquatic-society continuum in the northern Eurasian region. We introduce here the state of the art for the key topics in the PEEX research agenda and present the future prospects of the research, which we see relevant in this context.
[1] In situ measurements of the vertical distribution of carbon dioxide (CO 2 ) carried out with a light aircraft over a tower site (Berezorechka; 56°08′45″N, 84°19′49″E) in the taiga region of West Siberia from October 2001 to March 2012 document the detailed seasonal and vertical variation of CO 2 concentrations during daytime. The variation appears to be controlled mainly by the CO 2 flux from taiga ecosystems and the height of the planetary boundary layer (PBL). We calculated average CO 2 concentrations in the PBL and the lower free troposphere (LFT), both of which show clear seasonal cycles and an increasing long-term trend. Seasonal amplitude in the PBL had a larger value (29 ppm) than that in the LFT (14 ppm), demonstrating strong CO 2 source-sink forcing by the taiga ecosystems. Mean CO 2 concentrations during 13:00-17:00 local standard time observed at the four levels of the tower (5, 20, 40, and 80 m) showed lower CO 2 concentrations than that observed in the PBL by aircraft during June-August (growing season). This negative bias decreased with increasing inlet height such that the minimum difference appeared at the 80-m inlet (À2.4 ± 0.8 ppm). No such bias was observed during other months (dormant season). The daytime CO 2 flux, based on multiple vertical profiles obtained on a single day, ranged from À36.4 to 3.8 μmol m À2 s À1 during July-September. There was a clear difference in the fluxes between the morning and afternoon, suggesting that these data should be considered examples of fluxes during several daytime hours from the West Siberian taiga.
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