Fallout and concentration of aerosol-borne radioactivity over the Atlantic (Appendix)

Measurements of atmospheric radioactivity attached to aerosols are described. Fallout was collected in a vessel of large area. Emphasis was on separation of "wet" and "dry" samples. For strontium 90 a ratio of "wet" to "dry" fallout of 5:1 has been found independent of latitude. The total fallout was smaller than comparable values from continents because of very small amounts of rainfall in the equatorial zone. In order to achieve consistency in the global balance a better knowledge not only of radioactivity but also of precipitation over the ocean is required. Fallout of Ra-D clearly shows the ITC as a barrier for the latitudinal movement of near sea-surface air masses. The concentration of short-lived emanation daughters shows large variations according to varying geographic conditions. A variation with time could not be explained. The specific activity of long-lived radioactive substances shows the expected effect of the ITC as well as a seasonal diminuation of average concentration, similar to that measured at Heidelberg.

Continuous 25-years aerosol records at coastal Antarctica: Part I. Variability and climate implications of ionic compounds

The aerosol climatology at the coastal Antarctic Neumayer Station (NM) was investigated based on continuous, 25-yr long observations of biogenic sulphur components (methanesulfonate and non-sea salt sulphate), sea salt and nitrate. Although significant long-term trends could only be detected for nitrate (-3.6 ± 2.5% per year between 1983 and 1993 and +4.0 ± 3.2% per year from 1993-2007), non-harmonic periodicities between 2 and 5 yr were typical for all species. Dedicated time series analyses revealed that relations to sea ice extent and various circulation indices are weak at best or not significant. In particular, no consistent link between sea ice extent and sea salt loadings was evident suggesting only a rather local relevance of the NM sea salt record. Nevertheless, a higher Southern Annular Mode index tended to entail a lower biogenic sulphur signal. In examining the spatial uniformity of the NM findings we contrasted them to respective 17 yr records from the coastal Dumont d'Urville Station. We found similar long-term trends for nitrate, indicating an Antarctic-wide but not identifiable atmospheric signal, although any significant impact of solar activity or pollution could be ruled out. No inter-site variability on the multiannual scale was evident for the other ionic compounds.

Time series of black carbon aerosol measurements from Neumayer Station, 1999-2011

Continuous black carbon (BC) observations were conducted from 1999 through 2009 by an Aethalometer (AE10) and from 2006 through 2011 by a Multi-Angle Absorption Photometer (MAAP) at Neumayer Station (NM) under stringent contamination control. Considering the respective observation period, BC concentrations measured by the MAAP were somewhat higher (median ± standard deviation: 2.1 ± 2.0 ng/m**3) compared to the AE10 results (1.6 ± 2.1 ng/m**3). Neither for the AE10 nor for the MAAP data set a significant long-term trend could be detected. Consistently a pronounced seasonality was observed with both instruments showing a primary annual maximum between October and November and a minimum in April with a maximum/minimum ratio of 4.5/1.6 = 3.8 and 2.7/0.64 = 4.2 for the MAAP and AE10 data, respectively. Occasionally a secondary summer maximum in January/February was visible. With the aim to assess the impact of BC on optical properties of the aerosol at NM, we evaluated the BC data along with particle scattering coefficients measured by an integrating nephelometer. We found the mean single scattering albedo of w550 = 0.992 ± 0.0090 (median: 0.994) at a wavelength of 550 nm with a range of values from 0.95 to 1.0.

Trace elements in the aerosol at Neumayer Station, Antarctica

Atmospheric trace element concentrations were measured from March 1999 through December 2003 at the Air Chemistry Observatory of the German Antarctic station Neumayer by inductively coupled plasma - quadrupol mass spectrometry (ICP-QMS) and ion chromatogra-phy (IC). This continuous five year long record derived from weekly aerosol sampling re-vealed a distinct seasonal summer maximum for elements linked with mineral dust entry (Al, La, Ce, Nd) and a winter maximum for the mostly sea salt derived elements Li, Na, K, Mg, Ca, and Sr. The relative seasonal amplitude was around 1.7 and 1.4 for mineral dust (La) and sea salt aerosol (Na), respectively. On average a significant deviation regarding mean ocean water composition was apparent for Li, Mg, and Sr which could hardly be explained by mir-abilite precipitation on freshly formed sea ice. In addition we observed all over the year a not clarified high variability of element ratios Li/Na, K/Na, Mg/Na, Ca/Na, and Sr/Na. We found an intriguing co-variation of Se concentrations with biogenic sulfur aerosols (methane sul-fonate and non-sea salt sulfate), indicating a dominant marine biogenic source for this element linked with the marine biogenic sulfur source.

Contents of Ag, Bi, In, and Tl in suspended and aerosol matter at Station DM8-579 in the Peru Basin, Southeast Pacific

A new electrothermal atomizer for use in direct determination of Ag, Bi, In, and Tl in marine, riverine, and aeolian particulate matter on membrane filters is described. A sample capsule and atomization cell are heated separately. That is why it is possible to separate and optimize decomposition of a sample, vaporization of elements and atomization of their vapors. Noise reduction and design, which localizes the vapors in a light absorption zone, decrease detection limits of these four elements by factor of at least 3 to 10. Some analytical results are given.

The sulphate component in aerosol samples over the Noth Atlantic Ocean (Tab. 1)

The size distribution of sulphate containing particles over the North Atlantic was determined for particles with radii larger than 0.18 µm. It is compared with the size distributions of the total aerosol, the hygroscopic and the insoluble parts in the maritime aerosol. From mass concentrations of sulphate and sodium, it can be concluded that only a fraction of sulphate originates from the ocean. The sulphate mass distribution separated into its sea salt sulphate and excess sulphate components is compared with a continental distribution.