Abstract. We have performed new calculations of the radiative forcing due to changes in the concentrations of the most important well mixed greenhouse gases (WMGG) since pre-industrial time. Three radiative transfer models are used. The radiative forcing due to CO2, including shortwave absorption, is 15% lower than the previous IPCC estimate. The radiative forcing due to all the WMGG is calculated to 2.25 Wm -2, which we estimate to be accurate to within about 5%. The importance of the CFCs is increased by about 20% relative to the total effect of all WMGG compared to previous estimates. We present updates to simple forcingconcentration relationships previously used by IPCC.

New calculations of the radiative forcing (RF) are presented for the three main well‐mixed greenhouse gases, methane, nitrous oxide, and carbon dioxide. Methane's RF is particularly impacted because of the inclusion of the shortwave forcing; the 1750–2011 RF is about 25% higher (increasing from 0.48 W m−2 to 0.61 W m−2) compared to the value in the Intergovernmental Panel on Climate Change (IPCC) 2013 assessment; the 100 year global warming potential is 14% higher than the IPCC value. We present new simplified expressions to calculate RF. Unlike previous expressions used by IPCC, the new ones include the overlap between CO2 and N2O; for N2O forcing, the CO2 overlap can be as important as the CH4 overlap. The 1750–2011 CO2 RF is within 1% of IPCC's value but is about 10% higher when CO2 amounts reach 2000 ppm, a value projected to be possible under the extended RCP8.5 scenario.

[1] The physical and optical properties of Saharan dust aerosol measured by the Met Office C-130 during the Saharan Dust Experiment (SHADE) are presented. Additional radiation measurements enable the determination of the aerosol optical depth, t aerl , and the direct radiative effect (DRE) of the mineral dust. The results suggest that the absorption by Saharan dust is significantly overestimated in the solar spectrum if standard refractive indices are used. Our measurements suggest an imaginary part of the refractive index of 0.0015i is appropriate at a wavelength l of 0.55 mm. Different methods for determining t aerl=0.55 are presented, and the accuracy of each retrieval method is assessed. The value t aerl=0.55 is estimated as 1.48 ± 0.05 during the period of heaviest dust loading, which is derived from an instantaneous DRE of approximately À129 ± 5 Wm À2 or an enhancement of the local planetary albedo over ocean of a factor of 2.7 ± 0.1. A comparison of the DRE derived from the C-130 instrumentation and from the Clouds and the Earth's Radiant Energy System (CERES) instrument on the Tropical Rainfall Measuring Mission (TRMM) satellite is presented; the results generally showing agreement to within a factor of 1.2. The results suggest that Saharan dust aerosol exerts the largest local and global DRE of all aerosol species and should be considered explicitly in global radiation budget studies.

This paper presents data on elemental and mineralogical composition of mineral dust from various source regions of Africa collected during the African Monsoon Multidisciplinary Analyses (AMMA) SOP0/DABEX and Dust Ouflow and Deposition to the Ocean (DODO) DODO1 experiments (January–February 2006), and the DODO2 campaign (August 2006). Bulk filter samples were collected at the AMMA supersite of Banizoumbou, Niger, as well as on board the Facility for Airborne Atmospheric Measurements (FAAM) BAe‐146 aircraft. Both mineral dust and biomass burning in external mixing occurred in surface and elevated layers during the winter field phase of the campaign. However, mineral dust was overwhelming, accounting for 72% of the estimated aerosol mass in aged elevated biomass burning layers and up to 93% in plumes of mineral dust, which generally occurred in the boundary layer. A number of well‐defined episodes of advection of mineral dust could be identified both at the ground and on the aircraft. The elemental and mineralogical composition varied depending on source region. This variability could be well traced by the calcium content, which is enhanced in dust from North Africa but depleted in dust from the Sahel. Iron oxides in the form of hematite and goethite are enriched in dust emitted within Sahel and in Mauritania, whereas dust from the Bodélé depression is iron‐oxide depleted. Iron oxides represented between 2.4% and 4.5% of the total estimated dust oxide mass. This regional variability will have to be taken into account in estimating the optical properties of absorption of mineral dust from western Africa.

[1] The African Monsoon Multidisciplinary Analysis (AMMA) is a major international campaign investigating far-reaching aspects of the African monsoon, climate and the hydrological cycle. A special observing period was established for the dry season (SOP0) with a focus on aerosol and radiation measurements. SOP0 took place during January and February 2006 and involved several ground-based measurement sites across west Africa. These were augmented by aircraft measurements made by the Facility for Airborne Atmospheric Measurements (FAAM) aircraft during the Dust and Biomass-burning Experiment (DABEX), measurements from an ultralight aircraft, and dedicated modeling efforts. We provide an overview of these measurement and modeling studies together with an analysis of the meteorological conditions that determined the aerosol transport and link the results together to provide a balanced synthesis. The biomass burning aerosol was significantly more absorbing than that measured in other areas and, unlike industrial areas, the ratio of excess carbon monoxide to organic carbon was invariant, which may be owing to interaction between the organic carbon and mineral dust aerosol. The mineral dust aerosol in situ filter measurements close to Niamey reveals very little absorption, while other measurements and remote sensing inversions suggest significantly more absorption. The influence of both mineral dust and biomass burning aerosol on the radiation budget is significant throughout the period, implying that meteorological models should include their radiative effects for accurate weather forecasts and climate simulations. Generally, the operational meteorological models that simulate the production and transport of mineral dust show skill at lead times of 5 days or more. Climate models that need to accurately simulate the vertical profiles of both anthropogenic and natural aerosols to accurately represent the direct and indirect effects of aerosols appear to do a reasonable job, although the magnitude of the aerosol scattering is strongly dependent upon the emission data set.