Unveiling aerosol–cloud interactions – Part 1: Cloud contamination in satellite products enhances the aerosol indirect forcing estimate

Atmospheric Chemistry and Physics European Geosciences Union 17:21 (2017) 13151-13164

Authors:

Matthew Christensen, D Neubauer, CA Poulsen, GE Thomas, Gregory R McGarragh, AC Povey, Simon R Proud, Roy G Grainger

Abstract:

Increased concentrations of aerosol can enhance the albedo of warm low-level cloud. Accurately quantifying this relationship from space is challenging due in part to contamination of aerosol statistics near clouds. Aerosol retrievals near clouds can be influenced by stray cloud particles in areas assumed to be cloud-free, particle swelling by humidification, shadows and enhanced scattering into the aerosol field from (3-D radiative transfer) clouds. To screen for this contamination we have developed a new cloud–aerosol pairing algorithm (CAPA) to link cloud observations to the nearest aerosol retrieval within the satellite image. The distance between each aerosol retrieval and nearest cloud is also computed in CAPA.

Results from two independent satellite imagers, the Advanced Along-Track Scanning Radiometer (AATSR) and Moderate Resolution Imaging Spectroradiometer (MODIS), show a marked reduction in the strength of the intrinsic aerosol indirect radiative forcing when selecting aerosol pairs that are located farther away from the clouds (−0.28±0.26 W m−2) compared to those including pairs that are within 15 km of the nearest cloud (−0.49±0.18 W m−2). The larger aerosol optical depths in closer proximity to cloud artificially enhance the relationship between aerosol-loading, cloud albedo, and cloud fraction. These results suggest that previous satellite-based radiative forcing estimates represented in key climate reports may be exaggerated due to the inclusion of retrieval artefacts in the aerosol located near clouds.

The Community Cloud retrieval for CLimate (CC4CL). Part II: The optimal estimation approach

Atmospheric Measurement Techniques Discussions European Geosciences Union (2017)

Authors:

Gregory McGarragh, CA Poulsen, Gareth E Thomas, Adam C Povey, O Sus, S Stapelberg, C Schlundt, Simon R Proud, Matthew W Christensen, M Stengel, R Hollmann, Roy Grainger

Abstract:

The Community Cloud retrieval for Climate (CC4CL) is a cloud property retrieval system for satellite-based multispectral imagers and is an important component of the Cloud Climate Change Initiative (Cloud_cci) project. In this paper we discuss the optimal estimation retrieval of cloud optical thickness, effective radius and cloud top pressure based on the Optimal Retrieval of Aerosol and Cloud (ORAC) algorithm. Key to this method is the forward model which, includes the 5 clear-sky model, the liquid water and ice cloud models, the surface model including a bidirectional reflectance distribution function (BRDF), the “fast” radiative transfer solution (which includes a multiple scattering treatment) All of these components and their assumptions and limitations will be discussed in detail. The forward model provides the accuracy appropriate for our retrieval method. The errors are comparable to the instrument noise for cloud optical thicknesses greater than 10. At optical thicknesses less than 10 modelling errors become more significant. The retrieval method is then presented describing 10 optimal estimation in general, the non-linear inversion method employed, measurement and a priori inputs, the propagation of input uncertainties and the calculation of subsidiary quantities that are derived from the retrieval results. An evaluation of the retrieval was performed using measurements simulated with noise levels appropriate for the MODIS instrument. Results show errors less than 10% for cloud optical thicknesses greater than 10. Results for clouds of optical thicknesses less than 10 have errors ranging up to 20%.

Mass extinction spectra and size distribution measurements of quartz and amorphous silica aerosol at 0.33-19 mu m compared to modelled extinction using Mie, CDE, and T-matrix theories

JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER 199 (2017) 52-65

Authors:

BE Reed, DM Peters, R McPheat, AJA Smith, RG Grainger

Balloon-borne measurement of the aerosol size distribution from an Icelandic flood basalt eruption

Earth and Planetary Science Letters Elsevier 453 (2017) 252-259

Authors:

D Vignelles, TJ Roberts, E Carboni, E Ilyinskaya, M Pfeffer, P Dagsson Waldhauserova, A Schmidt, G Berthet, F Jegou, J-B Renard, H Ólafsson, B Bergsson, R Yeo, N Fannar Reynisson, Roy Grainger, B Galle, V Conde, S Arellano, T Lurton, B Coute, V Duverger

Abstract:

We present in situ balloon-borne measurements of aerosols in a volcanic plume made during the Holuhraun eruption (Iceland) in January 2015. The balloon flight intercepted a young plume at 8 km distance downwind from the crater, where the plume is ∼15 min of age. The balloon carried a novel miniature optical particle counter LOAC (Light Optical Aerosol Counter) which measures particle number concentration and size distribution in the plume, alongside a meteorological payload. We discuss the possibility of calculating particle flux by combining LOAC data with measurements of sulfur dioxide flux by ground-based UV spectrometer (DOAS). The balloon passed through the plume at altitude range of 2.0–3.1 km above sea level (a.s.l.). The plume top height was determined as 2.7–3.1 km a.s.l., which is in good agreement with data from Infrared Atmospheric Sounding Interferometer (IASI) satellite. Two distinct plume layers were detected, a non-condensed lower layer (300 m thickness) and a condensed upper layer (800 m thickness). The lower layer was characterized by a lognormal size distribution of fine particles (0.2 μm diameter) and a secondary, coarser mode (2.3 μm diameter), with a total particle number concentration of around 100 cm −3 in the 0.2–100 μm detection range. The upper layer was dominated by particle centered on 20 μm in diameter as well as containing a finer mode (2 μm diameter). The total particle number concentration in the upper plume layer was an order of magnitude higher than in the lower layer. We demonstrate that intercepting a volcanic plume with a meteorological balloon carrying LOAC is an efficient method to characterize volcanic aerosol properties. During future volcanic eruptions, balloon-borne measurements could be carried out easily and rapidly over a large spatial area in order to better characterize the evolution of the particle size distribution and particle number concentrations in a volcanic plume.

Retrieval of volcanic SO2 from HIRS/2 using optimal estimation

ATMOSPHERIC MEASUREMENT TECHNIQUES 10:7 (2017) 2687-2702

Authors:

GM Miles, R Siddans, RG Grainger, AJ Prata, B Fisher, N Krotkov