Corrigendum to "Global and regional emission estimates for HCFC-22", Atmos. Chem. Phys., 12, 10033–10050, 2012

No abstract available

Hydro Aluminium AS. Measurements of CF4 and C2F6 emissions from Norsk Hydro's aluminium smelter at Husnes, Norway.

NILU and Hydro Aluminium performed a test campaign for measurements of CF4 and C2F6 for stack emissions at Husnes Aluminium Smelter. Time-integrated samples were taken with evacuated canisters combined with low-flow restrictors for continuous sampling periods as long as 6 weeks. The samples were analyzed at NILU with a Medusa preconcentration method combined with GC-MS SIM. As a main conclusion, time integrated sampling together with Medusa GC-MS methodology is a very precise alternative to the traditional attempts to quantify PFC-emission

Tracing biomass burning aerosol from South America to Troll Research Station, Antarctica

The atmospheric observatory at the Norwegian Research Station Troll in Queen Maud Land, Antarctica, holds, since February 2007, the first all-year Antarctic atmospheric aerosol particle number size distribution measurements. These are colocated with measurements of the aerosol absorption and spectral scattering coefficients. In June 2007, this instrument set observed an aerosol whose properties were indicative of a biomass burning aerosol. These properties included two log-normal size distribution modes with median particle diameters of 0.105 μm and 0.36 μm, sharply falling off to smaller and larger sizes, and peaks in scattering and absorption coefficient. With backward plume calculations of the Lagrangian transport model FLEXPART and the MODIS fire activity product, a source-receptor relationship was established between biomass burning events in Central Brazil and the aerosol seen at Troll. This is the first direct evidence that the Antarctic continent is susceptible to emissions from as far north as Southern tropical latitudes

Long-term monitoring of persistent organic pollutants (POPs) at the Norwegian Troll station in Dronning Maud Land, Antarctica

A first long-term monitoring of selected persistent organic pollutants (POPs) in Antarctic air has been conducted at the Norwegian research station Troll (Dronning Maud Land). As target contaminants 32 PCB congeners, α- and γ-hexachlorocyclohexane (HCH), trans- and cis-chlordane, trans- and cis-nonachlor, p,p'- and o,p-DDT, DDD, DDE as well as hexachlorobenzene (HCB) were selected. The monitoring program with weekly samples taken during the period 2007–2010 was coordinated with the parallel program at the Norwegian Arctic monitoring site (Zeppelin mountain, Ny-Ålesund, Svalbard) in terms of priority compounds, sampling schedule as well as analytical methods. The POP concentration levels found in Antarctica were considerably lower than Arctic atmospheric background concentrations. Similar to observations for Arctic samples, HCB is the predominant POP compound, with levels of around 22 pg m−3 throughout the entire monitoring period. In general, the following concentration distribution was found for the Troll samples analyzed: HCB > Sum HCH > Sum PCB > Sum DDT > Sum chlordanes. Atmospheric long-range transport was identified as a major contamination source for POPs in Antarctic environments. Several long-range transport events with elevated levels of pesticides and/or compounds with industrial sources were identified based on retroplume calculations with a Lagrangian particle dispersion model (FLEXPART)

Monitoring of greenhouse gases and aerosols at Svalbard and Birkenes in 2014 - Annual report.

The report summaries the activities and results of the greenhouse gas monitoring at the Zeppelin Observatory situated on Svalbard in Arctic Norway during the period 2001-2014, and the greenhouse gas monitoring and aerosol observations from Birkenes for 2009-2014

Consumption of CH3Cl, CH3Br, and CH3I and emission of CHCl3, CHBr3, and CH2Br2 from the forefield of a retreating Arctic glacier

The Arctic is one of the most rapidly warming regions of the Earth, with predicted temperature increases of 5–7 ∘C and the accompanying extensive retreat of Arctic glacial systems by 2100. Retreating glaciers will reveal new land surfaces for microbial colonisation, ultimately succeeding to tundra over decades to centuries. An unexplored dimension to these changes is the impact upon the emission and consumption of halogenated organic compounds (halocarbons). Halocarbons are involved in several important atmospheric processes, including ozone destruction, and despite considerable research, uncertainties remain in the natural cycles of some of these compounds. Using flux chambers, we measured halocarbon fluxes across the glacier forefield (the area between the present-day position of a glacier's ice-front and that at the last glacial maximum) of a high-Arctic glacier in Svalbard, spanning recently exposed sediments (<10 years) to approximately 1950-year-old tundra. Forefield land surfaces were found to consume methyl chloride (CH3Cl) and methyl bromide (CH3Br), with both consumption and emission of methyl iodide (CH3I) observed. Bromoform (CHBr3) and dibromomethane (CH2Br2) have rarely been measured from terrestrial sources but were here found to be emitted across the forefield. Novel measurements conducted on terrestrial cyanobacterial mats covering relatively young surfaces showed similar measured fluxes to the oldest, vegetated tundra sites for CH3Cl, CH3Br, and CH3I (which were consumed) and for CHCl3 and CHBr3 (which were emitted). Consumption rates of CH3Cl and CH3Br and emission rates of CHCl3 from tundra and cyanobacterial mat sites were within the ranges reported from older and more established Arctic tundra elsewhere. Rough calculations showed total emissions and consumptions of these gases across the Arctic were small relative to other sources and sinks due to the small surface area represented by glacier forefields. We have demonstrated that glacier forefields can consume and emit halocarbons despite their young age and low soil development, particularly when cyanobacterial mats are present