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During the 35th Indian Scientific Expedition to Antarctica, measurements of atmospheric carbon dioxide (CO 2 ) were carried out using a Li-Cor CO 2 /H 2 O analyser at Bharati, the Indian Antarctic research station. This study examines the short-term variability of atmospheric CO 2 during the austral summer (January–February) of 2016. An average of 396.25 ± 4.20 ppm was observed during the study period. Meteorological parameters such as relative humidity, precipitation, wind speed, air temperature and atmospheric boundary layer height in conjunction with photosynthetically active radiation, the biological activity indicator which modulates atmospheric CO 2 concentration have been investigated. High wind speed (>20 m s −1 ) combined with precipitation scavenges CO 2 in the atmosphere, resulting in low concentrations at the study site. The lowest CO 2 concentration of 385 ppm coincided with heavy precipitation of 15 mm during study period. Statistical analysis of the data shows that precipitation and relative humidity independently correlated 55% (r = −0.55) and 32% (r = −0.32), respectively, with the variability of CO 2 mixing in the atmosphere at the study site. Atmospheric CO 2 was significantly correlated with precipitation alone with a p value of 0.003. Further, multiple regression analysis was performed to test the significant relation between variability of atmospheric CO 2 and meteorological parameters. Long-range air-mass transport analysis depicted that the majority of the air masses are reaching the study site through the oceanic region.

This study aimed to quantify the nitrous oxide (N2O) and methane (CH4) fluxes at sites with different vegetation covers and where bird activity was present or absent using the static chamber method, on Rip Point, Nelson Island, maritime Antarctic. The sites were soils covered by Sanionia uncinata, lichens, Prasiola crispa, Deschampsia antarctica and bare soil. Seabirds used the P. crispa and D. antarctica sites as nesting areas. Soil mineral N contents, air and soil temperature and water-filled pore space were measured, and the content of total organic C and particulate organic C, total N, bulk density and texture were determined to identify controlling variables of the gas emissions. The N2O and CH4 flux rates were low for all sampling events. Mean N2O flux rates ranged from 0.11±1.93 up to 21.25±22.14 µg N2O m−2 h−1 for the soils under lichen and P. crispa cover, respectively. For the CH4 fluxes, only the P. crispa site showed a low positive mean (0.47±3.61 µg CH4 m−2 h−1). The bare soil showed the greatest absorption of CH4 (−11.92±5.7 µg CH4 m−2 h−1), probably favoured by the coarse soil texture. Bare soil and S. uncinata sites had N2O accumulated emissions close to zero. Net CH4 accumulated emission was observed only at the P. crispa site, which was correlated with (p<0.001). These results indicate that seabird activity influences N2O and CH4 soil fluxes, while vegetation has little influence, and bare soil areas in maritime Antarctica could be greenhouse gas sinks. Keywords: Soil greenhouse gases; seabirds; vegetal cover; maritime Antarctica.

A large volcanic eruption might constitute a climate emergency, significantly altering global temperature and precipitation for several years. Major future eruptions will occur, but their size or timing cannot be predicted. We show, for the first time, that it may be possible to counteract these climate effects through deliberate emissions of short-lived greenhouse gases, dampening the abrupt impact of an eruption. We estimate an emission pathway countering a hypothetical eruption 3 times the size of Mount Pinatubo in 1991. We use a global climate model to evaluate global and regional responses to the eruption, with and without counteremissions. We then raise practical, financial, and ethical questions related to such a strategy. Unlike the more commonly discussed geoengineering to mitigate warming from long-lived greenhouse gases, designed emissions to counter temporary cooling would not have the disadvantage of needing to be sustained over long periods. Nevertheless, implementation would still face significant challenges.

We use observations of N2O and mean age to identify realistic transport in models in order to explain their ozone predictions. The results are applied to 15 chemistry climate models (CCMs) participating in the 2010 World Meteorological Organization ozone assessment. Comparison of the observed and simulated N2O, mean age and their compact correlation identifies models with fast or slow circulations and reveals details of model ascent and tropical isolation. This process-oriented diagnostic is more useful than mean age alone because it identifies models with compensating transport deficiencies that produce fortuitous agreement with mean age. The diagnosed model transport behavior is related to a model's ability to produce realistic lower stratosphere (LS) O3 profiles. Models with the greatest tropical transport problems compare poorly with O3 observations. Models with the most realistic LS transport agree more closely with LS observations and each other. We incorporate the results of the chemistry evaluations in the Stratospheric Processes and their Role in Climate (SPARC) CCMVal Report to explain the range of CCM predictions for the return-to-1980 dates for global (60°S–60°N) and Antarctic column ozone. Antarctic O3 return dates are generally correlated with vortex Cly levels, and vortex Cly is generally correlated with the model's circulation, although model Cl chemistry and conservation problems also have a significant effect on return date. In both regions, models with good LS transport and chemistry produce a smaller range of predictions for the return-to-1980 ozone values. This study suggests that the current range of predicted return dates is unnecessarily broad due to identifiable model deficiencies.

We report on ground-based atmospheric measurements and emission estimates of the four anthropogenic hydrofluorocarbons (HFCs) HFC-365mfc (CH3CF2CH2CF3, 1,1,1,3,3-pentafluorobutane), HFC-245fa (CHF2CH2CF3, 1,1,1,3,3-pentafluoropropane), HFC-227ea (CF3CHFCF3, 1,1,1,2,3,3,3-heptafluoropropane), and HFC-236fa (CF3CH2CF3, 1,1,1,3,3,3-hexafluoropropane). In situ measurements are from the global monitoring sites of the Advanced Global Atmospheric Gases Experiment (AGAGE), the System for Observations of Halogenated Greenhouse Gases in Europe (SOGE), and Gosan (South Korea). We include the first halocarbon flask sample measurements from the Antarctic research stations King Sejong and Troll. We also present measurements of archived air samples from both hemispheres back to the 1970s. We use a two-dimensional atmospheric transport model to simulate global atmospheric abundances and to estimate global emissions. HFC-365mfc and HFC-245fa first appeared in the atmosphere only ∼1 decade ago; they have grown rapidly to globally averaged dry air mole fractions of 0.53 ppt (in parts per trillion, 10−12) and 1.1 ppt, respectively, by the end of 2010. In contrast, HFC-227ea first appeared in the global atmosphere in the 1980s and has since grown to ∼0.58 ppt. We report the first measurements of HFC-236fa in the atmosphere. This long-lived compound was present in the atmosphere at only 0.074 ppt in 2010. All four substances exhibit yearly growth rates of >8% yr−1 at the end of 2010. We find rapidly increasing emissions for the foam-blowing compounds HFC-365mfc and HFC-245fa starting in ∼2002. After peaking in 2006 (HFC-365mfc: 3.2 kt yr−1, HFC-245fa: 6.5 kt yr−1), emissions began to decline. Our results for these two compounds suggest that recent estimates from long-term projections (to the late 21st century) have strongly overestimated emissions for the early years of the projections (∼2005–2010). Global HFC-227ea and HFC-236fa emissions have grown to average values of 2.4 kt yr−1 and 0.18 kt yr−1 over the 2008–2010 period, respectively.