During springtime in the polar regions, unique photochemistry converts inert halide salt ions (e.g. Br⁻) into reactive halogen species (e.g. Br atoms and BrO) that deplete ozone in the boundary layer to near zero levels. Since their discovery in the late 1980s, research on ozone depletion events (ODEs) has made great advances; however many key processes remain poorly understood. In this article we review the history, chemistry, dependence on environmental conditions, and impacts of ODEs. This research has shown the central role of bromine photochemistry, but how salts are transported from the ocean and are oxidized to become reactive halogen species in the air is still not fully understood. Halogens other than bromine (chlorine and iodine) are also activated through incompletely understood mechanisms that are probably coupled to bromine chemistry. The main consequence of halogen activation is chemical destruction of ozone, which removes the primary precursor of atmospheric oxidation, and generation of reactive halogen atoms/oxides that become the primary oxidizing species. The different reactivity of halogens as compared to OH and ozone has broad impacts on atmospheric chemistry, including near complete removal and deposition of mercury, alteration of oxidation fates for organic gases, and export of bromine into the free troposphere. Recent changes in the climate of the Arctic and state of the Arctic sea ice cover are likely to have strong effects on halogen activation and ODEs; however, more research is needed to make meaningful predictions of these changes

Abstract. During springtime in the polar regions, unique photochemistry converts inert halide salts ions (e.g. Br−) into reactive halogen species (e.g. Br atoms and BrO) that deplete ozone in the boundary layer to near zero levels. Since their discovery in the late 1980s, research on ozone depletion events (ODEs) has made great advances; however many key processes remain poorly understood. In this article we review the history, chemistry, dependence on environmental conditions, and impacts of ODEs. This research has shown the central role of bromine photochemistry, but how salts are transported from the ocean and are oxidized to become reactive halogen species in the air is still not fully understood. Halogens other than bromine (chlorine and iodine) are also activated through incompletely understood mechanisms that are probably coupled to bromine chemistry. The main consequence of halogen activation is chemical destruction of ozone, which removes the primary precursor of atmospheric oxidation, and generation of reactive halogen atoms/oxides that become the primary oxidizing species. The different reactivity of halogens as compared to OH and ozone has broad impacts on atmospheric chemistry, including near complete removal and deposition of mercury, alteration of oxidation fates for organic gases, and export of bromine into the free troposphere. Recent changes in the climate of the Arctic and state of the Arctic sea ice cover are likely to have strong effects on halogen activation and ODEs; however, more research is needed to make meaningful predictions of these changes.

Methane (CH) is a powerful greenhouse gas and plays a key part in global atmospheric chemistry. Natural geological emissions (fossil methane vented naturally from marine and terrestrial seeps and mud volcanoes) are thought to contribute around 52 teragrams of methane per year to the global methane source, about 10 per cent of the total, but both bottom-up methods (measuring emissions) and top-down approaches (measuring atmospheric mole fractions and isotopes) for constraining these geological emissions have been associated with large uncertainties. Here we use ice core measurements to quantify the absolute amount of radiocarbon-containing methane (CH) in the past atmosphere and show that geological methane emissions were no higher than 15.4 teragrams per year (95 per cent confidence), averaged over the abrupt warming event that occurred between the Younger Dryas and Preboreal intervals, approximately 11,600 years ago. Assuming that past geological methane emissions were no lower than today, our results indicate that current estimates of today's natural geological methane emissions (about 52 teragrams per year) are too high and, by extension, that current estimates of anthropogenic fossil methane emissions are too low. Our results also improve on and confirm earlier findings that the rapid increase of about 50 per cent in mole fraction of atmospheric methane at the Younger Dryas-Preboreal event was driven by contemporaneous methane from sources such as wetlands; our findings constrain the contribution from old carbon reservoirs (marine methane hydrates, permafrost and methane trapped under ice) to 19 per cent or less (95 per cent confidence). To the extent that the characteristics of the most recent deglaciation and the Younger Dryas-Preboreal warming are comparable to those of the current anthropogenic warming, our measurements suggest that large future atmospheric releases of methane from old carbon sources are unlikely to occur.

The cause of a large increase of atmospheric methane concentration during the Younger Dryas-Preboreal abrupt climatic transition (approximately 11,600 years ago) has been the subject of much debate. The carbon-14 (14C) content of methane (14CH4) should distinguish between wetland and clathrate contributions to this increase. We present measurements of 14CH4 in glacial ice, targeting this transition, performed by using ice samples obtained from an ablation site in west Greenland. Measured 14CH4 values were higher than predicted under any scenario. Sample 14CH4 appears to be elevated by direct cosmogenic 14C production in ice. 14C of CO was measured to better understand this process and correct the sample 14CH4. Corrected results suggest that wetland sources were likely responsible for the majority of the Younger Dryas-Preboreal CH4 rise.

Measurements of near-sea-level tropospheric D 14

Abstract. We present descriptions of the in situ instrumentation, calibration procedures, intercomparison efforts, and data filtering methods used in a 39-yr record of continuous atmospheric carbon dioxide (CO 2 ) observations made at Baring Head, New Zealand. Located on the southern coast of the North Island, Baring Head is exposed to extended periods of strong air flow from the south with minimal terrestrial influence resulting in low CO 2 variability. The site is therefore well suited for sampling air masses that are representative of the Southern Ocean region. Instrumental precision is better than 0.015 ppm (1-σ ) on 1-Hz values. Comparisons to over 600 co-located flask samples, as well as laboratory based flask and cylinder comparison exercises, suggest that over recent decades compatibility with respect to the Scripps Institution of Oceanography (SIO) and World Meteorological Organisation (WMO) CO 2 scales has been 0.3 ppm or better.

Mammals perceive the five different taste qualities: bitter, sweet, umami, sour, and salty. At least two different mechanisms contribute to salt taste in rodents. One is elicited by various cations and sensitive to cetylpyridinium chloride, whereas another is selectively stimulated by Na + and inhibited by amiloride. The latter pathway has been suggested to involve the epithelial sodium channel, ENaC. In humans, the presence of amiloride-sensitive salt taste transduction is being disputed. In this paper, we addressed the question whether ENaC may have a role in human salt taste perception. Immunohistochemistry revealed that β-, γ-, and δ-ENaC subunits are present in subsets of circumvallate and fungiform taste bud cells, whereas α-ENaC was confined to cells of circumvallate taste buds. Alpha-, β-, and γ-subunits were observed in basolateral intracellular compartments, while δ-ENaC was exclusively found in all taste pores of both types of papillae consistent with a function in taste transduction. To further assess the involvement of ENaC in salt taste transduction, we combined sensory studies and functional expression of ENaC in oocytes. With the exception of L-homoarginine, choline chloride, L-arginine, L-lysine, and L-argininyl-Larginine enhanced both salt taste perception in subjects and sodium currents recorded in αβγ-or δβγ-ENaC expressing oocytes, whereas L-glutamine did neither show salttaste-enhancing activity nor did it influence the sodium currents in the oocyte assay. Taken together, our data make ENaC an interesting molecule possibly involved in salty taste transduction.

Abstract. We present an analysis of a 39-year record of continuous atmospheric CO2 observations made at Baring Head, New Zealand, filtered for steady background CO2 mole fractions during southerly wind conditions. We discuss relationships between variability in the filtered CO2 time series and regional to global carbon cycling. Baring Head is well situated to sample air that has been isolated from terrestrial influences over the Southern Ocean, and experiences extended episodes of strong southerly winds with low CO2 variability. The filtered Baring Head CO2 record reveals an average seasonal cycle with amplitude of 0.95 ppm that is 13% smaller and 3 weeks earlier in phase than that at the South Pole. Seasonal variations in a given year are sensitive to the timing and magnitude of the combined influences of Southern Ocean CO2 fluxes and terrestrial fluxes from both hemispheres. The amplitude of the seasonal cycle varies throughout the record, but we find no significant long-term seasonal changes with respect to the South Pole. Interannual variations in CO2 growth rate in the Baring Head record closely match the El Niño-Southern Oscillation, reflecting the global reach of CO2 mole fraction anomalies associated with this cycle. We use atmospheric transport model results to investigate contributions to seasonal and annual-mean components of the observed CO2 record. Long-term trends in mean gradients between Baring Head and other stations are predominately due to increases in Northern Hemisphere fossil-fuel burning and Southern Ocean CO2 uptake, for which there remains a wide range of future estimates. We find that the postulated recent reduction in the efficiency of Southern Ocean anthropogenic CO2 uptake, as a result of increased zonal winds, is too small to be detectable as significant differences in atmospheric CO2 between mid to high latitude Southern Hemisphere observing stations.