RESUMEN

Industrial chlorofluorocarbons that cause ozone depletion have been phased out under the Montreal Protocol. A chemically driven increase in polar ozone (or "healing") is expected in response to this historic agreement. Observations and model calculations together indicate that healing of the Antarctic ozone layer has now begun to occur during the month of September. Fingerprints of September healing since 2000 include (i) increases in ozone column amounts, (ii) changes in the vertical profile of ozone concentration, and (iii) decreases in the areal extent of the ozone hole. Along with chemistry, dynamical and temperature changes have contributed to the healing but could represent feedbacks to chemistry. Volcanic eruptions have episodically interfered with healing, particularly during 2015, when a record October ozone hole occurred after the Calbuco eruption.

Asunto(s)

Clorofluorocarburos/química , Pérdida de Ozono , Erupciones Volcánicas , Regiones Antárticas , Modelos Teóricos , Estaciones del Año

RESUMEN

Antarctic ozone depletion is associated with enhanced chlorine from anthropogenic chlorofluorocarbons and heterogeneous chemistry under cold conditions. The deep Antarctic "hole" contrasts with the generally weaker depletions observed in the warmer Arctic. An unusually cold Arctic stratospheric season occurred in 2011, raising the question of how the Arctic ozone chemistry in that year compares with others. We show that the averaged depletions near 20 km across the cold part of each pole are deeper in Antarctica than in the Arctic for all years, although 2011 Arctic values do rival those seen in less-depleted years in Antarctica. We focus not only on averages but also on extremes, to address whether or not Arctic ozone depletion can be as extreme as that observed in the Antarctic. This information provides unique insights into the contrasts between Arctic and Antarctic ozone chemistry. We show that extreme Antarctic ozone minima fall to or below 0.1 parts per million by volume (ppmv) at 18 and 20 km (about 70 and 50 mbar) whereas the lowest Arctic ozone values are about 0.5 ppmv at these altitudes. At a higher altitude of 24 km (30-mbar level), no Arctic data below about 2 ppmv have been observed, including in 2011, in contrast to values more than an order of magnitude lower in Antarctica. The data show that the lowest ozone values are associated with temperatures below -80 °C to -85 °C depending upon altitude, and are closely associated with reduced gaseous nitric acid concentrations due to uptake and/or sedimentation in polar stratospheric cloud particles.

Asunto(s)

Pérdida de Ozono , Regiones Antárticas , Regiones Árticas , Atmósfera , Comunicaciones por Satélite , Estaciones del Año , Ozono Estratosférico/análisis , Temperatura

RESUMEN

Nitrogen trifluoride (NF(3)) has potential to make a growing contribution to the Earth's radiative budget; however, our understanding of its atmospheric burden and emission rates has been limited. Based on a revision of our previous calibration and using an expanded set of atmospheric measurements together with an atmospheric model and inverse method, we estimate that the global emissions of NF(3) in 2011 were 1.18 ± 0.21 Gg⋅y(-1), or ∼20 Tg CO(2)-eq⋅y(-1) (carbon dioxide equivalent emissions based on a 100-y global warming potential of 16,600 for NF(3)). The 2011 global mean tropospheric dry air mole fraction was 0.86 ± 0.04 parts per trillion, resulting from an average emissions growth rate of 0.09 Gg⋅y(-2) over the prior decade. In terms of CO(2) equivalents, current NF(3) emissions represent between 17% and 36% of the emissions of other long-lived fluorinated compounds from electronics manufacture. We also estimate that the emissions benefit of using NF(3) over hexafluoroethane (C(2)F(6)) in electronics manufacture is significant-emissions of between 53 and 220 Tg CO(2)-eq⋅y(-1) were avoided during 2011. Despite these savings, total NF(3) emissions, currently ∼10% of production, are still significantly larger than expected assuming global implementation of ideal industrial practices. As such, there is a continuing need for improvements in NF(3) emissions reduction strategies to keep pace with its increasing use and to slow its rising contribution to anthropogenic climate forcing.

RESUMEN

We present an analytical method for the in situ measurement of atmospheric nitrogen trifluoride (NF(3)), an anthropogenic gas with a 100-year global warming potential of over 16,000. This potent greenhouse gas has a rising atmospheric abundance due to its emission from a growing number of manufacturing processes and an expanding end-use market. Here we present a modified version of the "Medusa" preconcentration gas chromatography/mass spectrometry (GC/MS) system of Miller, B. R.; Weiss, R. F.; Salameh, P. K.; Tanhua, T.; Greally, B. R.; Mühle, J.; Simmonds, P. G. Anal. Chem.2008, 80 (5), 1536-1545. By altering the techniques of gas separation and chromatography after initial preconcentration, we are now able to make atmospheric measurements of NF(3) with relative precision <2% (1σ) for current background clean air samples. Importantly, this method augments the currently operational Medusa system, so that the quality of data for species already being measured is not compromised and NF(3) is measured from the same preconcentrated sample. We present the first in situ measurements of NF(3) from La Jolla, California made 11 times daily, illustrating how global deployment of this technique within the AGAGE (Advanced Global Atmospheric Gases Experiment) network could facilitate estimation of global and regional NF(3) emissions over the coming years.