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    Deviations from a general nonlinear wind balance: Local and zonal-mean perspectives
    (Stuttgart : Gebrüder Bornträger Verlagsbuchhandlung, 2014) Gassmann, A.
    The paper introduces the active wind as the deviation from a general local wind balance, the inactive wind. The inactive wind is directed along intersection lines of Bernoulli function and potential temperature surfaces. In climatological steady state, the inactive mass flux cannot participate in net-mass fluxes, because the mean position of the mentioned intersection lines does not change. A conceptual proximity of the zonal-mean active wind to the residual wind as occurring in the transformed Eulerian mean equations suggests itself. The zonaland time-mean active wind is compared to the residual wind for the Held-Suarez test case. Similarities occur for the meridional components in the zone of Rossby wave breaking in the upper troposphere equatorward of the jet. The vertical components are similar, too. However, the vertical active wind is much stronger in the baroclinic zone. This is due to the missing vertical eddy flux of Ertel's potential vorticity (EPV) in the TEM equations. The largest differences are to be found in the boundary layer, where the active wind exhibits typical pattern of Ekman dynamics. Instantaneous active wind vectors demonstrate mass-inflow for lows and mass-outflow for highs in the boundary layer. An active meridional wind is associated with a filamentation of EPV in the zone of Rossby wave breaking in about 300 hPa. Strong gradients of EPV act as a transport barrier.
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    The HadGEM2-ES implementation of CMIP5 centennial simulations
    (Göttingen : Copernicus, 2011) Jones, C.D.; Hughes, J.K.; Bellouin, N.; Hardiman, S.C.; Jones, G.S.; Knight, J.; Liddicoat, S.; O'Connor, F.M.; Andres, R.J.; Bell, C.; Boo, K.-O.; Bozzo, A.; Butchart, N.; Cadule, P.; Corbin, K.D.; Doutriaux-Boucher, M.; Friedlingstein, P.; Gornall, J.; Gray, L.; Halloran, P.R.; Hurtt, G.; Ingram, W.J.; Lamarque, J.-F.; Law, R.M.; Meinshausen, M.; Osprey, S.; Palin, E.J.; Parsons, Chini, L.; Raddatz, T.; Sanderson, M.G.; Sellar, A.A.; Schurer, A.; Valdes, P.; Wood, N.; Woodward, S.; Yoshioka, M.; Zerroukat, M.
    The scientific understanding of the Earth's climate system, including thecentral question of how the climate system is likely to respond tohuman-induced perturbations, is comprehensively captured in GCMs and EarthSystem Models (ESM). Diagnosing the simulated climate response, andcomparing responses across different models, is crucially dependent ontransparent assumptions of how the GCM/ESM has been driven - especiallybecause the implementation can involve subjective decisions and may differbetween modelling groups performing the same experiment. This paper outlinesthe climate forcings and setup of the Met Office Hadley Centre ESM, HadGEM2-ES for the CMIP5 set of centennial experiments. We document theprescribed greenhouse gas concentrations, aerosol precursors, stratosphericand tropospheric ozone assumptions, as well as implementation of land-usechange and natural forcings for the HadGEM2-ES historical and futureexperiments following the Representative Concentration Pathways. Inaddition, we provide details of how HadGEM2-ES ensemble members wereinitialised from the control run and how the palaeoclimate and AMIPexperiments, as well as the "emission-driven" RCP experiments wereperformed.
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    Direct estimation of the global distribution of vertical velocity within cirrus clouds
    (London : Nature Publishing Group, 2017) Barahona, Donifan; Molod, Andrea; Kalesse, Heike
    Cirrus clouds determine the radiative balance of the upper troposphere and the transport of water vapor across the tropopause. The representation of vertical wind velocity, W, in atmospheric models constitutes the largest source of uncertainty in the calculation of the cirrus formation rate. Using global atmospheric simulations with a spatial resolution of 7 km we obtain for the first time a direct estimate of the distribution of W at the scale relevant for cirrus formation, validated against long-term observations at two different ground sites. The standard deviation in W, σ w, varies widely over the globe with the highest values resulting from orographic uplift and convection, and the lowest occurring in the Arctic. Globally about 90% of the simulated σ w values are below 0.1 m s-1 and about one in 104 cloud formation events occur in environments with σ w > 0.8 m s-1. Combining our estimate with reanalysis products and an advanced cloud formation scheme results in lower homogeneous ice nucleation frequency than previously reported, and a decreasing average ice crystal concentration with decreasing temperature. These features are in agreement with observations and suggest that the correct parameterization of σ w is critical to simulate realistic cirrus properties.
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    Alberta wildfire 2016: Apt contribution from anomalous planetary wave dynamics
    ([London] : Macmillan Publishers Limited, part of Springer Nature, 2018) Petoukhov, Vladimir; Petri, Stefan; Kornhuber, Kai; Thonicke, Kirsten; Coumou, Dim; Schellnhuber, Hans Joachim
    In May-June 2016 the Canadian Province of Alberta suffered one of the most devastating wildfires in its history. Here we show that in mid-April to early May 2016 the large-scale circulation in the mid- and high troposphere of the middle and sub-polar latitudes of the northern hemisphere featured a persistent high-amplitude planetary wave structure dominated by the non-dimensional zonal wave number 4. The strongest anticyclonic wing of this structure was located over western Canada. In combination with a very strong El Niño event in winter 2015/2016 this favored highly anomalous, tinder-dry and high-temperature conditions at the surface in that area, entailing an increased fire hazard there. This critically contributed to the ignition of the Alberta Wildfire in May 2016, appearing to be the costliest disaster in Canadian history thus far.
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    Diurnal variation of midlatitudinal NO3 column abundance over table mountain facility, California
    (Göttingen : Copernicus GmbH, 2011) Chen, C.M.; Cageao, R.P.; Lawrence, L.; Stutz, J.; Salawitch, R.J.; Jourdain, L.; Li, Q.; Sander, S.P.
    The column abundance of NO3 was measured over Table Mountain Facility, CA (34.4° 117.7° W) from May 2003 through September 2004, using lunar occultation near full moon with a grating spectrometer. The NO 3 column retrieval was performed with the differential optical absorption spectroscopy (DOAS) technique using both the 623 and 662 nm NO 3 absorption bands. Other spectral features such as Fraunhofer lines and absorption from water vapor and oxygen were removed using solar spectra obtained at different airmass factors. We observed a seasonal variation, with nocturnally averaged NO3 columns between 5-7 × 1013 molec cm-2 during October through March, and 5-22 × 10 13 molec cm-2 during April through September. A subset of the data, with diurnal variability vastly different from the temporal profile obtained from one-dimensional stratospheric model calculations, clearly has boundary layer contributions; this was confirmed by simultaneous long-path DOAS measurements. However, even the NO3 columns that did follow the modeled time evolution were often much larger than modeled stratospheric partial columns constrained by realistic temperatures and ozone concentrations. This discrepancy is attributed to substantial tropospheric NO3 in the free troposphere, which may have the same time dependence as stratospheric NO 3.
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    Profiling water vapor mixing ratios in Finland by means of a Raman lidar, a satellite and a model
    (Katlenburg-Lindau : Copernicus, 2017) Filioglou, Maria; Nikandrova, Anna; Niemelä, Sami; Baars, Holger; Mielonen, Tero; Leskinen, Ari; Brus, David; Romakkaniemi, Sami; Giannakaki, Elina; Komppula, Mika
    We present tropospheric water vapor profiles measured with a Raman lidar during three field campaigns held in Finland. Co-located radio soundings are available throughout the period for the calibration of the lidar signals. We investigate the possibility of calibrating the lidar water vapor profiles in the absence of co-existing on-site soundings using water vapor profiles from the combined Advanced InfraRed Sounder (AIRS) and the Advanced Microwave Sounding Unit (AMSU) satellite product; the Aire Limitée Adaptation dynamique Développement INternational and High Resolution Limited Area Model (ALADIN/HIRLAM) numerical weather prediction (NWP) system, and the nearest radio sounding station located 100 km away from the lidar site (only for the permanent location of the lidar). The uncertainties of the calibration factor derived from the soundings, the satellite and the model data are < 2.8, 7.4 and 3.9 %, respectively. We also include water vapor mixing ratio intercomparisons between the radio soundings and the various instruments/model for the period of the campaigns. A good agreement is observed for all comparisons with relative errors that do not exceed 50 % up to 8 km altitude in most cases. A 4-year seasonal analysis of vertical water vapor is also presented for the Kuopio site in Finland. During winter months, the air in Kuopio is dry (1.15±0.40 †kg-1); during summer it is wet (5.54±1.02 †kg-1); and at other times, the air is in an intermediate state. These are averaged values over the lowest 2 km in the atmosphere. Above that height a quick decrease in water vapor mixing ratios is observed, except during summer months where favorable atmospheric conditions enable higher mixing ratio values at higher altitudes. Lastly, the seasonal change in disagreement between the lidar and the model has been studied. The analysis showed that, on average, the model underestimates water vapor mixing ratios at high altitudes during spring and summer.
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    Polarization lidar: An extended three-signal calibration approach
    (Katlenburg-Lindau : Copernicus, 2019) Jimenez, Cristofer; Ansmann, Albert; Engelmann, Ronny; Haarig, Moritz; Schmidt, Jörg; Wandinger, Ulla
    We present a new formalism to calibrate a threesignal polarization lidar and to measure highly accurate height profiles of the volume linear depolarization ratios under realistic experimental conditions. The methodology considers elliptically polarized laser light, angular misalignment of the receiver unit with respect to the main polarization plane of the laser pulses, and cross talk among the receiver channels. A case study of a liquid-water cloud observation demonstrates the potential of the new technique. Long-term observations of the calibration parameters corroborate the robustness of the method and the long-term stability of the three-signal polarization lidar. A comparison with a second polarization lidar shows excellent agreement regarding the derived volume linear polarization ratios in different scenarios: A biomass burning smoke event throughout the troposphere and the lower stratosphere up to 16 km in height, a dust case, and also a cirrus cloud case. © Author(s) 2019.
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    Aircraft-based observations of isoprene-epoxydiol-derived secondary organic aerosol (IEPOX-SOA) in the tropical upper troposphere over the Amazon region
    (Katlenburg-Lindau : EGU, 2018) Schulz, Christiane; Schneider, Johannes; Amorim Holanda, Bruna; Appel, Oliver; Costa, Anja; de Sá, Suzane S.; Dreiling, Volker; Fütterer, Daniel; Jurkat-Witschas, Tina; Klimach, Thomas; Knote, Christoph; Krämer, Martina; Martin, Scot T.; Mertes, Stephan; Pöhlker, Mira L.; Sauer, Daniel; Voigt, Christiane; Walser, Adrian; Weinzierl, Bernadett; Ziereis, Helmut; Zöger, Martin; Andreae, Meinrat O.; Artaxo, Paulo; Machado, Luiz A. T.; Pöschl, Ulrich; Wendisch, Manfred; Borrmann, Stephan
    During the ACRIDICON-CHUVA field project (September-October 2014; based in Manaus, Brazil) aircraft-based in situ measurements of aerosol chemical composition were conducted in the tropical troposphere over the Amazon using the High Altitude and Long Range Research Aircraft (HALO), covering altitudes from the boundary layer (BL) height up to 14.4km. The submicron non-refractory aerosol was characterized by flash-vaporization/electron impact-ionization aerosol particle mass spectrometry. The results show that significant secondary organic aerosol (SOA) formation by isoprene oxidation products occurs in the upper troposphere (UT), leading to increased organic aerosol mass concentrations above 10km altitude. The median organic mass concentrations in the UT above 10km range between 1.0 and 2.5μgm-3 (referring to standard temperature and pressure; STP) with interquartile ranges of 0.6 to 3.2μgm-3 (STP), representing 78% of the total submicron non-refractory aerosol particle mass. The presence of isoprene-epoxydiol-derived secondary organic aerosol (IEPOX-SOA) was confirmed by marker peaks in the mass spectra. We estimate the contribution of IEPOX-SOA to the total organic aerosol in the UT to be about 20%. After isoprene emission from vegetation, oxidation processes occur at low altitudes and/or during transport to higher altitudes, which may lead to the formation of IEPOX (one oxidation product of isoprene). Reactive uptake or condensation of IEPOX on preexisting particles leads to IEPOX-SOA formation and subsequently increasing organic mass in the UT. This organic mass increase was accompanied by an increase in the nitrate mass concentrations, most likely due to NOx production by lightning. Analysis of the ion ratio of NO+ to NO2+ indicated that nitrate in the UT exists mainly in the form of organic nitrate. IEPOX-SOA and organic nitrates are coincident with each other, indicating that IEPOX-SOA forms in the UT either on acidic nitrate particles forming organic nitrates derived from IEPOX or on already neutralized organic nitrate aerosol particles.
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    Atmospheric new particle formation at the research station Melpitz, Germany: Connection with gaseous precursors and meteorological parameters
    (Katlenburg-Lindau : EGU, 2018) Größ, Johannes; Hamed, Amar; Sonntag, André; Spindler, Gerald; Manninen, Hanna Elina; Nieminen, Tuomo; Kulmala, Markku; Hõrrak, Urmas; Plass-Dülmer, Christian; Wiedensohler, Alfred; Birmili, Wolfram
    This paper revisits the atmospheric new particle formation (NPF) process in the polluted Central European troposphere, focusing on the connection with gas-phase precursors and meteorological parameters. Observations were made at the research station Melpitz (former East Germany) between 2008 and 2011 involving a neutral cluster and air ion spectrometer (NAIS). Particle formation events were classified by a new automated method based on the convolution integral of particle number concentration in the diameter interval 2-20 nm. To study the relevance of gaseous sulfuric acid as a precursor for nucleation, a proxy was derived on the basis of direct measurements during a 1-month campaign in May 2008. As a major result, the number concentration of freshly produced particles correlated significantly with the concentration of sulfur dioxide as the main precursor of sulfuric acid. The condensation sink, a factor potentially inhibiting NPF events, played a subordinate role only. The same held for experimentally determined ammonia concentrations. The analysis of meteorological parameters confirmed the absolute need for solar radiation to induce NPF events and demonstrated the presence of significant turbulence during those events. Due to its tight correlation with solar radiation, however, an independent effect of turbulence for NPF could not be established. Based on the diurnal evolution of aerosol, gas-phase, and meteorological parameters near the ground, we further conclude that the particle formation process is likely to start in elevated parts of the boundary layer rather than near ground level.
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    Vertical distribution of aerosol optical properties in the Po Valley during the 2012 summer campaigns
    (Katlenburg-Lindau : EGU, 2018) Bucci, Silvia; Cristofanelli, Paolo; Decesari, Stefano; Marinoni, Angela; Sandrini, Silvia; Größ, Johannes; Wiedensohler, Alfred; Di Marco, Chiara F.; Nemitz, Eiko; Cairo, Francesco; Di Liberto, Luca; Fierli, Federico
    Studying the vertical distribution of aerosol particle physical and chemical properties in the troposphere is essential to understand the relative importance of local emission processes vs. long-range transport for column-integrated aerosol properties (e.g. the aerosol optical depth, AOD, affecting regional climate) as well as for the aerosol burden and its impacts on air quality at the ground. The main objective of this paper is to investigate the transport of desert dust in the middle troposphere and its intrusion into the planetary boundary layer (PBL) over the Po Valley (Italy), a region considered one of the greatest European pollution hotspots for the frequency that particulate matter (PM) limit values are exceeded. Events of mineral aerosol uplift from local (soil) sources and phenomena of hygroscopic growth at the ground are also investigated, possibly affecting the PM concentration in the region as well. During the PEGASOS 2012 field campaign, an integrated observing-modelling system was set up based on near-surface measurements (particle concentration and chemistry), vertical profiling (backscatter coefficient profiles from lidar and radiosoundings) and Lagrangian air mass transport simulations by FLEXPART model. Measurements were taken at the San Pietro Capofiume supersite (44°39′ĝ€N, 11°37′ĝ€E; 11ĝ€mĝ€a.s.l.), located in a rural area relatively close to some major urban and industrial emissive areas in the Po Valley. Mt. Cimone (44°12′ĝ€N, 10°42′ĝ€E; 2165ĝ€mĝ€a.s.l.) WMO/GAW station observations are also included in the study to characterize regional-scale variability. Results show that, in the Po Valley, aerosol is detected mainly below 2000ĝ€mĝ€a.s.l. with a prevalent occurrence of non-depolarizing particles ( > 50ĝ€% throughout the campaign) and a vertical distribution modulated by the PBL daily evolution. Two intense events of mineral dust transport from northern Africa (19-21 and 29 June to 2 July) are observed, with layers advected mainly above 2000ĝ€m, but subsequently sinking and mixing in the PBL. As a consequence, a non-negligible occurrence of mineral dust is observed close to the ground ( ĝ1/4 7ĝ€% of occurrence during a 1-month campaign). The observations unambiguously show Saharan dust layers intruding the Po Valley mixing layer and directly affecting the aerosol concentrations near the surface. Finally, lidar observations also indicate strong variability in aerosol on shorter timescales (hourly). Firstly, these highlight events of hygroscopic growth of anthropogenic aerosol, visible as shallow layers of low depolarization near the ground. Such events are identified during early morning hours at high relative humidity (RH) conditions (RHĝ€ > 80ĝ€%). The process is observed concurrently with high PM1 nitrate concentration (up to 15ĝ€μgĝ€cmĝ'3) and hence mainly explicable by deliquescence of fine anthropogenic particles, and during mineral dust intrusion episodes, when water condensation on dust particles could instead represent the dominant contribution. Secondly, lidar images show frequent events (mean daily occurrence of ĝ1/4 ĝ€22ĝ€% during the whole campaign) of rapid uplift of mineral depolarizing particles in afternoon-evening hours up to 2000ĝ€mĝ€a.s.l. height. The origin of such particles cannot be directly related to long-range transport events, being instead likely linked to processes of soil particle resuspension from agricultural lands.