No abstract

[1] The AErosol RObotic NETwork (AERONET) estimates of instantaneous solar broadband fluxes (F) at surface have been validated through comparison with ground-based measurements of broadband fluxes at Mauna Loa Observatory (MLO) and by the Baseline Surface Radiation (BSRN) and the Solar Radiation Networks (SolRad-Net) during the period 1999-2005 and 1999-2006, respectively. The uncertainties in the calculated aerosol radiative forcing (DF) and radiative forcing efficiency (DF eff ) at the bottom of the atmosphere were also assessed. The stations have been selected attempting to cover different aerosols influences and hence radiative properties: urban-industrial, biomass burning, mineral dust, background continental, maritime aerosols and free troposphere. The AERONET solar downward fluxes at surface agree with ground-based measurements in all situations, with a correlation higher than 99% whereas the relation of observed to modeled fluxes ranges from 0.98 to 1.02. Globally an overestimation of 9 ± 12 Wm À2 of solar measurements was found, whereas for MLO (clear atmosphere) the differences decrease noticeably up to 2 ± 10 Wm À2 . The highest dispersion between AERONET estimates and measurements was observed in locations dominated by mineral dust and mixed aerosols types. In these locations, the F and DF uncertainties have shown a modest increase of the differences for high aerosol load, contrary to DF eff which are strongly affected by low aerosol load. Overall the discrepancies clustered within 9 ± 12 Wm À2 for DF and 28 ± 30 Wm À2 per unit of aerosol optical depth, t, at 0.55 mm for DF eff , where the latter is given for t(0.44 mm) ! 0.4. The error distributions have not shown any significant tendency with other aerosol radiative properties as well as size and shape particles.

Abstract. The shortwave radiative forcing ( F ) and the radiative forcing efficiency ( F eff ) of natural and anthropogenic aerosols have been analyzed using estimates of radiation both at the Top (TOA) and at the Bottom Of Atmosphere (BOA) modeled based on AERONET aerosol retrievals. Six main types of atmospheric aerosols have been compared (desert mineral dust, biomass burning, urbanindustrial, continental background, oceanic and free troposphere) in similar observational conditions (i.e., for solar zenith angles between 55 • and 65 • ) in order to compare the nearly same solar geometry. The instantaneous F averages obtained vary from −122 ± 37 Wm −2 (aerosol optical depth, AOD, at 0.55 µm, 0.85 ± 0.45) at the BOA for the mixture of desert mineral dust and biomass burning aerosols in West Africa and −42 ± 22 Wm −2 (AOD = 0.9 ± 0.5) at the TOA for the pure mineral dust also in this region up to −6 ± 3 Wm −2 and −4 ± 2 Wm −2 (AOD = 0.03 ± 0.02) at the BOA and the TOA, respectively, for free troposphere conditions. This last result may be taken as reference on a global scale. Furthermore, we observe that the more absorbing aerosols are overall more efficient at the BOA in contrast to at the TOA, where they backscatter less solar energy into the space. The analysis of the radiative balance at the TOA shows that, together with the amount of aerosols and their absorptive capacity, it is essential to consider the surface albedo of the region on which they are. Thus, we document that in regions with high surface reflectivity (deserts and snow conditions) atmospheric aerosols lead to a warming of the Earthatmosphere system.

[1] In July 2002 the VELETA-2002 field campaign was held in Sierra Nevada (Granada) in the south of Spain. The main objectives of this field campaign were the study of the influence of elevation and atmospheric aerosols on measured UV radiation. In the first stage of the field campaign, a common calibration and intercomparison between Licor-1800 spectroradiometers and Cimel-318 Sun photometers was performed in order to assess the quality of the measurements from the whole campaign. The intercomparison of the Licor spectroradiometers showed, for both direct and global irradiances, that when the comparisons were restricted to the visible part of the spectrum the deviations were within the instruments' nominal accuracies which allows us to rely on these instruments for measuring physical properties of aerosols at the different measurement stations. A simultaneous calibration on AOD data was performed for the Cimel-318 Sun photometers. When a common calibration and methodology was applied, the deviation was lowered to much less than 0.01 for AOD. At the same time an intercomparison has been made between the AOD values given by the spectroradiometers and the Sun photometers, with deviations obtained from 0.01 to 0.03 for the AOD in the visible range, depending on the channel. In the UVA range, the AOD uncertainty was estimated to be around 0.02 and 0.05 for Cimel and Licor respectively. In general the experimental differences were in agreement with this uncertainty estimation. In the UVB range the AOD measurements should not be used due to maximum instrumental uncertainties.

The shortwave radiative forcing (&Delta;<i>F</i>) and the radiative forcing efficiency (&Delta;<i>F</i>^eff) of natural and anthropogenic aerosols have been analyzed using estimates of radiation both at the top (TOA) and at the bottom of atmosphere (BOA) modeled based on AERONET aerosol retrievals. In this study we have considered six main types of atmospheric aerosols: desert mineral dust, biomass burning, urban-industrial, continental background, oceanic and free troposphere. The &Delta;<i>F</i> averages obtained vary from −148 ± 44 Wm⁻² (aerosol optical depth, AOD, at 0.55 μm, 0.85 ± 0.45) at the BOA for the mixture of desert mineral dust and biomass burning aerosols in Central Africa and −42 ± 22 Wm⁻² (AOD = 0.86 ± 0.51) at the TOA for the pure mineral dust also in this region up to −6 ± 3 Wm⁻² and −4 ± 2 Wm⁻² (AOD = 0.03 ± 0.02) at the BOA and the TOA, respectively, for free troposphere conditions. This last result may be taken as reference on a global scale. Furthermore, we observe that the more absorbing aerosols are overall more efficient at the BOA in contrast to at the TOA, where they backscatter less solar energy into the space. The analysis of the radiative balance at the TOA shows that, together with the amount of aerosols and their absorptive capacity, it is essential to consider the surface albedo of the region on which they are. Thus, we document that in regions with high surface reflectivity (deserts and snow conditions) atmospheric aerosols lead to a warming of the Earth-atmosphere system, contributing to the greenhouse gas effect

The complex orography of the Canary Islands favors the creation of microclimates, which cannot be studied using global climate models or regional models with moderate resolution. In this work, WRF is used to perform a dynamic climate regionalization in the archipelago, using the pseudo–global warming technique to compute the initial and boundary conditions from a reanalysis dataset and from results of 14 global climate models. The simulations were performed for three decades, one at present (1995–2004) and two in the future (2045–54 and 2090–99), and for two different greenhouse gas scenarios (RCP4.5 and RCP8.5), defined in phase 5 of the Coupled Model Intercomparison Project. The obtained results, at a 5-km horizontal resolution, show a clear dependence of temperature increase with height and a positive change in diurnal temperature range, which is mainly due to a reduction in soil moisture and a slight decrease in cloud cover. This negative change in soil moisture is mainly a consequence of a decrease in precipitation, although the evaluation of simulated reduction in precipitation does not show statistical significance in most of the Canary Islands for the analyzed periods and scenarios.

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Abstract. We report on measurements of atmospheric transmission (ATr) and aerosol optical depth (AODr) made at three wavelengths (368, 500, and 778 nm) with a spectroradiometer placed on Tenerife (28.5øN, 16.3øW), Canary Islands. Using the National Oceanic and Atmospheric Administration (NOAA) advanced very high resolution radiometer (AVHRR) channel 1, we also measured the aerosol optical depth (AODs) and albedo over a region of the North Atlantic Ocean extending from 15ø-35øN to 12ø-25øW. We observe large changes in ATr and AODr when dust outbreaks pass over this region. Using all these data, we derive the asymmetry factor (g), the single-scattering albedo (co), and the local mean AODr and we compute 'the direct radiative forcing AF attributable to mineral