scholarly journals Estimating cloud condensation nuclei concentrations from CALIPSO lidar measurements

2021 ◽  
Author(s):  
Goutam Choudhury ◽  
Matthias Tesche

Abstract. We present a novel methodology to estimate cloud condensation nuclei (CCN) concentrations from spaceborne CALIPSO lidar measurements. The algorithm utilizes (i) the CALIPSO-derived backscatter and extinction coefficient, depolarization ratio, and aerosol subtype information, (ii) the normalized volume size distributions and refractive indices from the CALIPSO aerosol model, and (iii) the MOPSMAP optical modelling package. For each CALIPSO height bin, we first select the aerosol-type specific size distribution and then adjust it to reproduce the extinction coefficient derived from the CALIPSO retrieval. The scaled size distribution is integrated to estimate the aerosol number concentration which is then used in the CCN parameterizations to calculate CCN concentrations at different supersaturations. To account for the hygroscopicity of continental and marine aerosols, we use the kappa parameterization and correct the size distributions before the scaling step. We have studied the sensitivity of the thus derived CCN concentration to the effect of variations of the initial size distributions. It is found that the uncertainty associated with the algorithm can range between a factor of 2 and 3. We have also compared our results with the POLIPHON and found comparable results for extinction coefficients larger than 0.05 km−1. An initial application to a case with coincident airborne in-situ measurements for independent validation shows promising results and illustrates the potential of CALIPSO for constructing a global height-resolved CCN climatology.

2019 ◽  
Vol 19 (24) ◽  
pp. 15483-15502 ◽  
Author(s):  
Yicheng Shen ◽  
Aki Virkkula ◽  
Aijun Ding ◽  
Krista Luoma ◽  
Helmi Keskinen ◽  
...  

Abstract. The concentration of cloud condensation nuclei (CCN) is an essential parameter affecting aerosol–cloud interactions within warm clouds. Long-term CCN number concentration (NCCN) data are scarce; there are a lot more data on aerosol optical properties (AOPs). It is therefore valuable to derive parameterizations for estimating NCCN from AOP measurements. Such parameterizations have already been made, and in the present work a new parameterization is presented. The relationships between NCCN, AOPs, and size distributions were investigated based on in situ measurement data from six stations in very different environments around the world. The relationships were used for deriving a parameterization that depends on the scattering Ångström exponent (SAE), backscatter fraction (BSF), and total scattering coefficient (σsp) of PM10 particles. The analysis first showed that the dependence of NCCN on supersaturation (SS) can be described by a logarithmic fit in the range SS <1.1 %, without any theoretical reasoning. The relationship between NCCN and AOPs was parameterized as NCCN≈((286±46)SAE ln(SS/(0.093±0.006))(BSF − BSFmin) + (5.2±3.3))σsp, where BSFmin is the minimum BSF, in practice the 1st percentile of BSF data at a site to be analyzed. At the lowest supersaturations of each site (SS ≈0.1 %), the average bias, defined as the ratio of the AOP-derived and measured NCCN, varied from ∼0.7 to ∼1.9 at most sites except at a Himalayan site where the bias was >4. At SS >0.4 % the average bias ranged from ∼0.7 to ∼1.3 at most sites. For the marine-aerosol-dominated site Ascension Island the bias was higher, ∼1.4–1.9. In other words, at SS >0.4 % NCCN was estimated with an average uncertainty of approximately 30 % by using nephelometer data. The biases were mainly due to the biases in the parameterization related to the scattering Ångström exponent (SAE). The squared correlation coefficients between the AOP-derived and measured NCCN varied from ∼0.5 to ∼0.8. To study the physical explanation of the relationships between NCCN and AOPs, lognormal unimodal particle size distributions were generated and NCCN and AOPs were calculated. The simulation showed that the relationships of NCCN and AOPs are affected by the geometric mean diameter and width of the size distribution and the activation diameter. The relationships of NCCN and AOPs were similar to those of the observed ones.


2016 ◽  
Vol 16 (18) ◽  
pp. 12059-12079 ◽  
Author(s):  
Luke B. Hande ◽  
Christa Engler ◽  
Corinna Hoose ◽  
Ina Tegen

Abstract. An aerosol model was used to simulate the generation and transport of aerosols over Germany during the HD(CP)2 Observational Prototype Experiment (HOPE) field campaign of 2013. The aerosol number concentrations and size distributions were evaluated against observations, which shows satisfactory agreement in the magnitude and temporal variability of the main aerosol contributors to cloud condensation nuclei (CCN) concentrations. From the modelled aerosol number concentrations, number concentrations of CCN were calculated as a function of vertical velocity using a comprehensive aerosol activation scheme which takes into account the influence of aerosol chemical and physical properties on CCN formation. There is a large amount of spatial variability in aerosol concentrations; however the resulting CCN concentrations vary significantly less over the domain. Temporal variability is large in both aerosols and CCN. A parameterization of the CCN number concentrations is developed for use in models. The technique involves defining a number of best fit functions to capture the dependence of CCN on vertical velocity at different pressure levels. In this way, aerosol chemical and physical properties as well as thermodynamic conditions are taken into account in the new CCN parameterization. A comparison between the parameterization and the CCN estimates from the model data shows excellent agreement. This parameterization may be used in other regions and time periods with a similar aerosol load; furthermore, the technique demonstrated here may be employed in regions dominated by different aerosol species.


2016 ◽  
Author(s):  
Luke B. Hande ◽  
Christa Engler ◽  
Corinna Hoose ◽  
Ina Tegen

Abstract. An aerosol model was used to simulate the generation and transportation of aerosols over Germany during the HD(CP)2 Observational Prototype Experiment (HOPE) field campaign of 2013. The aerosol number concentrations and size distributions were evaluated against observations, which shows satisfactory agreement in the magnitude and temporal variability of the main aerosol contributors to cloud condensation nuclei (CCN) concentrations. From the modelled aerosol number concentrations, number concentrations of CCN were calculated as a function of vertical velocity using a comprehensive aerosol activation scheme which takes into account the influence of aerosol chemical and physical properties on CCN formation. There is a large amount of spatial variability in aerosol concentrations, however the resulting CCN concentrations vary significantly less over the domain. Temporal variability is large in both aerosols and CCN. A parameterisation of the CCN number concentrations is developed for use in models. The technique involves defining a number of best fit functions to capture the dependence of CCN on vertical velocity at different pressure levels. In this way, aerosol chemical and physical properties as well as thermodynamic conditions are taken into account in the new CCN parameterisation. A comparison between the parameterisation and the CCN estimates from the model data shows excellent agreement. This parameterisation may be used in other regions and time periods with a similar aerosol load, and furthermore, this technique demonstrated here may be employed in regions dominated by different aerosol species.


2021 ◽  
Author(s):  
Goutam Choudhury ◽  
Matthias Tesche

&lt;p&gt;Aerosols interact with atmospheric radiation either directly through scattering and absorption or indirectly by acting as cloud condensation nuclei (CCN) and ice nucleating particles (INP), thereby altering cloud properties. The latter aerosol-cloud interaction (ACI) effects are still poorly understood and believed to be one of the key uncertainties in climate models. In the present scenario, the observations of CCN are still sparse as in-situ measurements are expensive and often restricted to specific locations and limited time periods. An alternative is to turn to satellite observations for ACI studies. The Cloud Aerosol Lidar with Orthogonal Polarisation (CALIOP) is a spaceborne lidar aboard the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) satellite. It provides high-resolution vertical profiles of aerosol related parameters such as the aerosol extinction coefficient, backscatter coefficient, aerosol subtypes, and depolarization ratio. In order to estimate the CCN concentrations, we use these parameters along with the normalised lognormal bimodal volume size distributions and complex refractive indices of different aerosol subtypes given in the CALISPO aerosol model.&lt;/p&gt;&lt;p&gt;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160;&amp;#160; The normalised size distribution, the refractive index and the relative humidity are first used to compute the extinction coefficient using the MOPSMAP package. For this, all the aerosol types are treated as spherical particles except the dust which is treated as spheroid. The size distribution is then modified until the estimated extinction agrees with that measured by the CALIPSO. The modified size distribution is integrated to compute the number concentration of aerosols that form the favourable CCN reservoir. To estimate the uncertainty in the retrieval algorithm, we performed the sensitivity analysis by varying the initial normalised volume size distribution by up to +/- 50 % for each mode (fine and coarse). The results are presented as case studies with some preliminary validation against in-situ measurements. The purpose of this work is to obtain a global 3D CCN climatology for use in ACI studies and improving the performance of the global climate models.&lt;/p&gt;


Atmosphere ◽  
2020 ◽  
Vol 11 (9) ◽  
pp. 912
Author(s):  
Ankang Liu ◽  
Honglei Wang ◽  
Yuanyuan Li ◽  
Yan Yin ◽  
Bin Li ◽  
...  

The aerosol size distribution and cloud condensation nuclei (CCN) number concentration were measured using a wide-range particle spectrometer (WPS) and a cloud condensation nuclei counter (CCNC) on Mt. Tian from 31 July to 9 September, 2019. Combined with meteorological data, distribution characteristics of aerosol size and CCN and their influencing factors were analyzed. The results indicated that the mean aerosol number concentration was 5475.6 ± 5636.5 cm−3. The mean CCN concentrations were 183.7 ± 114.5 cm−3, 729.8 ± 376.1 cm−3, 1630.5 ± 980.5 cm−3, 2162.5 ± 1345.3 cm−3, and 2575.7 ± 1632.9 cm−3 at supersaturation levels of 0.1%, 0.2%, 0.4%, 0.6%, and 0.8%, respectively. The aerosol number size distribution is unimodal, and the dominant particle size is 30–60 nm. Affected by the height of the boundary layer and the valley wind, the diurnal variation in aerosol number concentration shows a unimodal distribution with a peak at 17:00, and the CCN number concentration showed a bimodal distribution with peaks at 18:00 and 21:00. The particle size distribution and supersaturation have a major impact on the activation of the aerosol into CCN. At 0.1% supersaturation (S), the 300–500 nm particles are most likely to activate to CCN. Particles of 100–300 nm are most easily activated at 0.2% (S), while particles of 60–80 nm are most likely activated at high supersaturation (≥0.4%). The concentrations of aerosol and CCN are higher in the northerly wind. Ambient relative humidity (RH) has little relationship with the aerosol activation under high supersaturation. According to N = CSk fitting the CCN spectrum, C = 3297 and k = 0.90 on Mt. Tian, characteristic of the clean continental type.


2012 ◽  
Vol 12 (1) ◽  
pp. 623-689 ◽  
Author(s):  
G. W. Mann ◽  
K. S. Carslaw ◽  
D. A. Ridley ◽  
D. V. Spracklen ◽  
K. J. Pringle ◽  
...  

Abstract. A global modal aerosol microphysics module (GLOMAP-mode) is evaluated and improved by comparing against a sectional version (GLOMAP-bin) and observations in the same 3-D global offline chemistry transport model. With both schemes, the model captures the main features of the global particle size distribution, with sub-micron aerosol approximately unimodal in continental regions and bi-modal in marine regions. Initial bin-mode comparisons showed that various size distribution parameter settings (mode widths and inter-modal separation sizes) resulted in clear biases compared to the sectional scheme. By adjusting these parameters in the modal scheme, much better agreement is achieved against the bin scheme and observations. Surface mass of sulphate, sea-salt, black carbon (BC) and organic carbon (OC) are, on the annual mean, within 25 % in the two schemes in nearly all regions. On the annual mean, surface level concentrations of condensation nuclei (CN), cloud condensation nuclei (CCN), surface area density and condensation sink also compare within 25 % in most regions. However, marine CCN concentrations between 30° N and 30° S are systematically higher in the modal scheme, by 25–60 %, which we attribute to differences in size-resolved particle growth or cloud-processing. Larger differences also exist in regions or seasons dominated by biomass burning and in free-troposphere and high-latitude regions. Indeed, in the free-troposphere, GLOMAP-mode BC is a factor 2–4 higher than GLOMAP-bin, likely due to differences in size-resolved scavenging. Nevertheless, in most parts of the atmosphere, we conclude that bin-mode differences are much less than model-observation differences, although some processes are missing in these runs which may pose a bigger challenge to modal schemes (e.g. boundary layer nucleation, ultra-fine sea-spray). The findings here underline the need for a spectrum of complexity in global models, with size-resolved aerosol properties predicted by modal schemes needing to be continually benchmarked and improved against freely evolving sectional schemes and observations.


2019 ◽  
Vol 19 (13) ◽  
pp. 8845-8861 ◽  
Author(s):  
Juntao Wang ◽  
Yanjie Shen ◽  
Kai Li ◽  
Yang Gao ◽  
Huiwang Gao ◽  
...  

Abstract. Determination of the updated concentrations of atmospheric particles (Ncn) and the concentrations of cloud condensation nuclei (Nccn) over the northwestern Pacific Ocean (NWPO) are important to accurately evaluate the influence of aerosol outflow from the Asian continent on the climate by considering the rapid changes in emissions of air pollutants therein. However, field observations in the last two decades are scarce. We conducted a cruise campaign over the NWPO to simultaneously measure Ncn, Nccn and the size distribution of aerosol particles from day of year (DOY) 81 to DOY 108 of 2014. The mean values of Nccn at supersaturation (SS) of levels 0.2 % and 0.4 % were 0.68±0.38×103 and 1.1±0.67×103 cm−3, respectively, with an average of 2.8±1.0×103 cm−3 for Ncn during the cruise over the NWPO. All are approximately 1 order of magnitude larger than spring observations made during the preceding two decades in the remote marine atmosphere. The larger values, against the marine natural background reported in the literature, imply an overwhelming contribution from continental inputs. The calculated activity ratios (ARs) of the cloud condensation nuclei (CCN) were 0.30±0.11 and 0.46±0.19 at SS levels of 0.2 % and 0.4 %, respectively, which are almost the same as those of upwind semi-urban sites. High Nccn and CCN activities were observed from DOY 98 to DOY 102, when the oceanic zone received even stronger continental input. Excluding biomass burning (BB) and dust aerosols, good correlation between Nccn at 0.4 % SS and the number concentrations of > 60 nm particles (N>60 nm) was obtained during the entire cruise period, with a slope of 0.98 and R2=0.94, and the corresponding effective hygroscopicity parameter (κ) was estimated to be 0.40. A bimodal size distribution pattern of the particle number concentration was generally observed during the entire campaign when the N>90 nm varied largely. However, the N<30 nm, accounting for approximately one-third of the total number concentration, varied narrowly, and two NPF events associated with vertical transport were observed. This implies that a pool of nucleation-mode atmospheric particles is aloft. BB and dust events were observed over the NWPO, but their aerosol contributions to Ncn and Nccn were minor (i.e., 10 % or less) on a monthly timescale.


2017 ◽  
Author(s):  
Sebastian Düsing ◽  
Birgit Wehner ◽  
Patric Seifert ◽  
Albert Ansmann ◽  
Holger Baars ◽  
...  

Abstract. This study presents vertical profiles up to a height of 2300 m a.s.l. of aerosol microphysical and optical properties and cloud condensation nuclei (CCN). Corresponding data have been measured during a field campaign as part of the High-Definition Clouds and Precipitation for Advancing Climate Prediction (HD(CP)2) Observational Prototype Experiments (HOPE), which took place at Melpitz, Germany from September 9 to 29, 2013. The helicopter-borne payload ACTOS (Airborne Cloud and Turbulence Observation System) was used to determine the aerosol particle number size distribution (PNSD), the number concentrations of aerosol particles (PNC) and cloud condensation nuclei (CCN) (CCN-NC), the ambient relative humidity (RH), and temperature (T). Simultaneous measurements on ground provided a holistic view on aerosol microphysical properties such as the PNSD, the chemical composition and the CCN-NC. Additional measurements of a 3 + 2 wavelength polarization lidar system (PollyXT) provided profiles of the aerosol particle light backscatter coefficient (σbsc) for three wavelengths (355, 532 and 1064 nm). From profiles of σbsc profiles of the aerosol particle light extinction coefficient (σext) were determined using the extinction-to-backscatter ratio. Furthermore, CCN-NC profiles were estimated on basis of the lidar-measurements. Ambient state optical properties of aerosol particles were derived on the basis of airborne in situ measurements of ACTOS (PNSD) and in situ measurements on ground (chemical aerosol characterization) using Mie-theory. On the basis of ground-based and airborne measurements, this work investigates the representativeness of ground-based aerosol microphysical properties for the boundary layer for two case-studies. The PNSD measurements on ground showed a good agreement with the measurements provided with ACTOS for lower altitudes. The ground-based measurements of PNC and CCN-NC are representative for the PBL when the PBL is well mixed. Locally isolated new particle formation events on ground or at the top of the PBL led to vertical variability in the here presented cases and ground-based measurements are not representative for the PBL. Furthermore, the lidar-based estimates of CCN-NC profiles were compared with the airborne in situ measurements of ACTOS. This comparison showed good agreements within the uncertainty range. Finally, this work provides a closure study between the optical aerosol particle properties in ambient state based on the airborne ACTOS measurements and derived with the lidar measurements. The investigation of the optical properties shows for 14 measurement-points that the airborne-based particle light backscatter coefficient is for 1064 nm 50 % smaller than the measurements of the lidar system, 27.6 % smaller for 532 nm and 29.9 % smaller for 355 nm. These results are quite promising, since in-situ measurement based Mie-calculations of the particle light backscattering are scarce and the modelling is quite challenging. In contradiction for the particle light extinction coefficient retrieved from the airborne in situ measurements were found a good agreement. The airborne-based particle light extinction coefficient was just 7.9 % larger for 532 nm and 3.5 % smaller for 355 nm, for an assumed lidar ratio (LR) of 55 sr. The particle light extinction coefficient for 1064 nm was derived with a LR of 30 sr. For this wavelength, the airborne-based particle light extinction coefficient is 5.2 % smaller than the lidar-measurements. Also, the correlation for the particle light extinction coefficient in combination with Mie-based LR's are in agreement for typical LR's of European background aerosol.


2019 ◽  
Author(s):  
Samuel A. Atwood ◽  
Sonia M. Kreidenweis ◽  
Paul J. DeMott ◽  
Markus D. Petters ◽  
Gavin C. Cornwell ◽  
...  

Abstract. Aerosol particle and cloud condensation nuclei (CCN) measurements from a littoral location on the northern coast of California at Bodega Bay Marine Laboratory (BML) are presented for approximately six weeks of observations during the CalWater-2015 field campaign. A combination of aerosol microphysical and meteorological parameters was used to classify variability in the properties of the BML surface aerosol using a K-means cluster model. Eight aerosol population types were identified that were associated with a range of impacts from both marine and terrestrial sources. Average measured total particle number concentrations, size distributions, hygroscopicities, and activated fraction spectra between 0.08 % and 1.1 % supersaturation are given for each of the identified aerosol population types, along with meteorological observations and transport pathways during time periods associated with each type. Five terrestrially influenced aerosol population types represented different degrees of aging of the continental outflow from the coast and interior of California and their appearance at the BML site was often linked to changes in wind direction and transport pathway. In particular, distinct aerosol populations, associated with diurnal variations in source region induced by land/sea-breeze shifts, were classified by the clustering technique. A terrestrial type representing fresh emissions, and/or a recent new particle formation event, occurred in approximately 10 % of the observations. Over the entire study period, three marine influenced population types were identified that typically occurred when the regular diurnal land/sea-breeze cycle collapsed and BML was continuously ventilated by air masses from marine regions for multiple days. These marine types differed from each other primarily in the degree of cloud processing evident in the size distributions, and in the presence of an additional large-particle mode for the type associated with the highest wind speeds. One of the marine types was associated with a multi-day period during which an atmospheric river made landfall at BML. The generally higher total particle number concentrations but lower activated fractions of four of the terrestrial types yielded similar CCN number concentrations to two of the marine types for supersaturations below about 0.4 %. Despite quite different activated fraction spectra, the two remaining marine and terrestrial types had CCN spectral number concentrations very similar to each other, due in part to higher number concentrations associated with the terrestrial type.


Sign in / Sign up

Export Citation Format

Share Document