The <b>RE</b>gents <b>PAR</b>k and <b>T</b>ower <b>E</b>nvironmental <b>E</b>xperiment (REPARTEE) comprised two campaigns in London in October 2006 and October/November 2007. The experiment design involved measurements at a heavily trafficked roadside site, two urban background sites and an elevated site at 160–190 m above ground on the BT Tower, supplemented in the second campaign by Doppler lidar measurements of atmospheric vertical structure. A wide range of measurements of airborne particle physical metrics and chemical composition were made as well as measurements of a considerable range of gas phase species and the fluxes of both particulate and gas phase substances. Significant findings include (a) demonstration of the evaporation of traffic-generated nanoparticles during both horizontal and vertical atmospheric transport; (b) generation of a large base of information on the fluxes of nanoparticles, accumulation mode particles and specific chemical components of the aerosol and a range of gas phase species, as well as the elucidation of key processes and comparison with emissions inventories; (c) quantification of vertical gradients in selected aerosol and trace gas species which has demonstrated the important role of regional transport in influencing concentrations of sulphate, nitrate and secondary organic compounds within the atmosphere of London; (d) generation of new data on the atmospheric structure and turbulence above London, including the estimation of mixed layer depths; (e) provision of new data on trace gas dispersion in the urban atmosphere through the release of purposeful tracers; (f) the determination of spatial differences in aerosol particle size distributions and their interpretation in terms of sources and physico-chemical transformations; (g) studies of the nocturnal oxidation of nitrogen oxides and of the diurnal behaviour of nitrate aerosol in the urban atmosphere, and (h) new information on the chemical composition and source apportionment of particulate matter size fractions in the atmosphere of London derived both from bulk chemical analysis and aerosol mass spectrometry with two instrument types

Abstract. The NERC UK SOLAS-funded Reactive Halogens in the Marine Boundary Layer (RHaMBLe) programme comprised three field experiments. This manuscript presentsCorrespondence to: G. McFiggans (g.mcfiggans@manchester.ac.uk) an overview of the measurements made within the two simultaneous remote experiments conducted in the tropical North Atlantic in May and June 2007. Measurements were made from two mobile and one ground-based platforms. The heavily instrumented cruise D319 on the RRS Discovery from Lisbon, Portugal to São Vicente, Cape Verde and back to Falmouth, UK was used to characterise the spatial distribution Published by Copernicus Publications on behalf of the European Geosciences Union. of boundary layer components likely to play a role in reactive halogen chemistry. Measurements onboard the ARSF Dornier aircraft were used to allow the observations to be interpreted in the context of their vertical distribution and to confirm the interpretation of atmospheric structure in the vicinity of the Cape Verde islands. Long-term ground-based measurements at the Cape Verde Atmospheric Observatory (CVAO) on São Vicente were supplemented by long-term measurements of reactive halogen species and characterisation of additional trace gas and aerosol species during the intensive experimental period.This paper presents a summary of the measurements made within the RHaMBLe remote experiments and discusses them in their meteorological and chemical context as determined from these three platforms and from additional meteorological analyses. Air always arrived at the CVAO from the North East with a range of air mass origins (European, Atlantic and North American continental). Trace gases were present at stable and fairly low concentrations with the exception of a slight increase in some anthropogenic components in air of North American origin, though NO x mixing ratios during this period remained below 20 pptv (note the non-IUPAC adoption in this manuscript of pptv and ppbv, equivalent to pmol mol −1 and nmol mol −1 to reflect common practice). Consistency with these air mass classifications is observed in the time series of soluble gas and aerosol composition measurements, with additional identification of periods of slightly elevated dust concentrations consistent with the trajectories passing over the African continent. The CVAO is shown to be broadly representative of the wider North Atlantic marine boundary layer; measurements of NO, O 3 and black carbon from the ship are consistent with a clean Northern Hemisphere marine background. Aerosol composition measurements do not indicate elevated organic material associated with clean marine air. Closer to the African coast, black carbon and NO levels start to increase, indicating greater anthropogenic influence. Lower ozone in this region is possibly associated with the increased levels of measured halocarbons, associated with the nutrient rich waters of the Mauritanian upwelling. Bromide and chloride deficits in coarse mode aerosol at both the CVAO and on D319 and th...

Abstract. Broadband cavity enhanced absorption spectroscopy (BBCEAS) has been used to measure the sum of concentrations of NO 3 and N 2 O 5 from the BT (telecommunications) Tower 160 m above street level in central London during the REPARTEE II campaign in October and November 2007. Substantial variability was observed in these nighttime nitrogen compounds: peak NO 3 +N 2 O 5 mixing ratios reached 800 pptv, whereas the mean night-time NO 3 [O 3 ]. Co-measurements of temperature and NO 2 from the BT Tower were used to calculate the equilibrium partitioning between NO 3 and N 2 O 5 which was always found to strongly favour N 2 O 5 (NO 3 /N 2 O 5 =0.01 to 0.04). Two methods are used to calculate the lifetimes for NO 3 and N 2 O 5 , the results being compared and discussed in terms of the implications for the night-time oxidation of nitrogen oxides and the night-time sinks for NO y .

[1] Recent developments in ice melter systems and continuous flow analysis (CFA) techniques now allow higher-resolution ice core analysis. Here, we present a new method to aid interpretation of high-resolution ice core stable water isotope records. Using a set of simple isotopic recording and postdepositional assumptions, the European Centre for Medium-Range Weather Forecasts' 40 year reanalysis time series of temperature and precipitation are converted to "virtual core" depth series across the Antarctic Peninsula, helping us to understand what information can be gleaned from the CFA high-resolution observations. Virtual core temperatures are transferred onto time using three different depth-age transfer assumptions: (1) a perfect depth-age model, (2) a depth-age model constructed from single or dual annual photochemical tie points, and (3) a cross-dated depth-age model. Comparing the sampled temperatures on the various depth-age models with the original time series allows quantification of the effect of ice core sample resolution and dating. We show that accurate annual layer count depth-age models should allow some subseasonal temperature anomalies to be recovered using a sample resolution of around 40 mm, or 10-20 samples per year. Seasonal temperature anomalies may be recovered using sample lengths closer to 60 mm, or about 7-14 samples per year. These results tend to confirm the value of current CFA ice core sampling strategies and indicate that it should be possible to recover about a third of subannual (but not synoptic) temperature anomaly information from annually "layer-counted" peninsula ice cores.