Arctic Ozone Depletion Observed by UARS MLS during the 1994-95 Winter
The Arctic lower stratosphere was unusually cold and the polar vortex
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The Arctic lower stratosphere was unusually cold and the polar vortex
During the unusually cold 1994-95 Arctic winter, the Microwave Limb Sounder observed enhanced chlorine monoxide (ClO) in late Dec and throughout Feb and early Mar. Late Dec ClO was higher than during any of the previous 3 years, consistent with the colder early winter. Between late Dec 1994 and early Feb 1995, 465 K (about 50 hPa) vortex-averaged ozone (03) decreased by about 15%, with local decreases of about 30%; additional local decreases of about 5% were seen between early Feb and early Mar. Transport calculations indicate that vortex-averaged chemical loss between late Dec and early Feb was about 20% at 465 K, with about 1/4 of that masked by downward transport of O3. This Arctic chemical O3 loss is not readily detectable in MLS column O3 data.
We report on stratospheric and mesospheric water vapor (H2O) observations obtained by the Millimeter wave Atmospheric Sounder (MAS) in the Arctic spring of 1992. In the lower stratosphere, the observations show enhanced H2O inside the vortex between 450 K and 625 K, in agreement with other H2O observations. In the upper stratosphere and lower mesosphere, at potential temperatures between 1850 K and 2200 K, we find regions of depressed H2O volume mixing ratio coincident with remnants of high potential vorticity. The depressed mesospheric H2O, as well as the enhanced lower stratospheric H2O, are consistent with wintertime descent. It also suggests effective containment of air up into the lower mesosphere.
During the winter of 1999-2000, the AROTEL instrument was deployed on the NASA DC-8 at Kiruna, Sweden for the SAGE III Ozone Loss Validation Experiment (SOLVE). Measurements of ozone, temperature and aerosols were made on 18 local science flights from December to March. Extremely low temperatures were observed throughout most of the Arctic vortex and polar stratospheric clouds were observed throughout the Arctic area during January. Significant ozone loss was measured after the sun began to rise on the vortex area in February. Ozone mixing ratios as low as 800 ppbv were observed during flights in March.
Wintertime sea ice covers 15 million square kilometers of the north polar region, an area exceeding one and a half times the area of the U. S. Even at the end of the summer melt season, sea ice still covers 7 million square kilometers. This vast ice cover is an integral component of the climate system, being moved around by winds and waves, restricting heat and other exchanges between the ocean and atmosphere, reflecting most of the solar radiation incident on it, transporting cold, relatively fresh water equatorward, and affecting the overturning of ocean waters underneath, with impacts that can be felt worldwide. Sea ice also is a major factor in the Arctic ecosystem, affecting life forms ranging from minute organisms living within the ice, sometimes to the tune of millions in a single ice floe, to large marine mammals like walruses that rely on sea ice as a platform for resting, foraging, social interaction, and breeding. Since 1978, satellite technology has allowed the monitoring of the vast Arctic sea ice cover on a routine basis. The satellite observations reveal that, overall, the areal extent of Arctic sea ice has been decreasing since 1978, at an average rate of 2.7% per decade through the end of 1998. Through 1998, the greatest rates of decrease occurred in the Seas of Okhotsk and Japan and the Kara and Barents Seas, with most other regions of the Arctic also experiencing ice extent decreases. The two regions experiencing ice extent increases over this time period were the Bering Sea and the Gulf of St. Lawrence. Furthermore, the satellite data reveal that the sea ice season shortened by over 25 days per decade in the central Sea of Okhotsk and the eastern Barents Sea, and by lesser amounts throughout much of the rest of the Arctic seasonal sea ice region, although not in the Bering Sea or the Gulf of St. Lawrence. Concern has been raised that if the trends toward shortened sea ice seasons and lesser sea ice coverage continue, this could entail major consequences to the polar climate and to the lifestyles (and perhaps even the survivability) of polar bears and other polar species.
The ER-2 Condensation Nucleus Counter (ER-2 CNC) was operated in the Airborne Arctic Stratospheric Expedition (AASE) in January and February 1989. The ER-2 CNC measures the mixing ratio of particles, CN, with diameters from approximately 0.02 to approximately 1 micron. The spatial distribution of CN in the Arctic polar vortex was found to resemble that measured in the Antarctic in the Spring of 1987. The vertical profile of CN in the vortex was lowered by subsidence. At altitudes above the minimum in the CN mixing ratio profile, CN mixing ratios correlated negatively with that of N2O, demonstrating new particle production. CN serve as nuclei in the formation of Polar Stratospheric Clouds (PSCs) and the concentration of CN can affect PSC properties.
Using recently developed techniques we estimate snow and sea ice thickness distributions for the Arctic basin through the combination of freeboard data from the Ice, Cloud, and land Elevation Satellite (ICESat) and a snow depth model. These data are used with meteorological data and a thermodynamic sea ice model to calculate ocean-atmosphere heat exchange and ice volume production during the 2003-2008 fall and winter seasons. The calculated heat fluxes and ice growth rates are in agreement with previous observations over multiyear ice. In this study, we calculate heat fluxes and ice growth rates for the full distribution of ice thicknesses covering the Arctic basin and determine the impact of ice thickness change on the calculated values. Thinning of the sea ice is observed which greatly increases the 2005-2007 fall period ocean-atmosphere heat fluxes compared to those observed in 2003. Although there was also a decline in sea ice thickness for the winter periods, the winter time heat flux was found to be less impacted by the observed changes in ice thickness. A large increase in the net Arctic ocean-atmosphere heat output is also observed in the fall periods due to changes in the areal coverage of sea ice. The anomalously low sea ice coverage in 2007 led to a net ocean-atmosphere heat output approximately 3 times greater than was observed in previous years and suggests that sea ice losses are now playing a role in increasing surface air temperatures in the Arctic.
During the Arctic Airborne Stratospheric Expedition (AASE) simultaneous measurements of aerosol size distribution and NO(y)(HN03 + NO + NO2 + 2(N205)) were made along ER-2 flight paths. The flow characteristics of the NO(y) instrument allow us to derive the condensed NO(y) amount (assumed to be HN03) present during polar stratospheric cloud (PSC) events. Analysis of the January 24th flight indicates that this condensed HN03 amount does not agree well with the aerosol volume if the observed PSCs are composed of solid nitric acid trihydrate (NAT), as is generally assumed. However, the composition agrees well with that predicted for liquid H2S04/HN03/H20 solution droplets using a new Aerosol Physical Chemistry Model (APCM). The agreement corresponds in detail to variations in temperature and humidity. The weight percentages of H2SO4, HN03, and H2O derived from the measurements all correspond to those predicted for ternary, liquid solutions.
Ozone mixing ratios in the vicinity of the 525-K potential temperature surface in January and early February of 1990 were observed to decrease sharply across the edge of the vortex boundary, where the vortex position was estimated from Ertel's potential vorticity. The changes in NO(y) mixing ratio with respect to altitude measured on January 18 and 31 were quite well correlated with those of ozone between 15 and 24 km, indicating that NO(y) also had a large gradient across the edge of the vortex. This is interpreted as being mainly due to the significant denitrification that occurred inside the vortex. The total amount of gas and particulate phase HNO3 was close to the NO(y) amount at the altitude of the 22- to 23-km region, suggesting that the conversion of non-HNO3 reactive nitrogen to HNO3 had occurred with a PSC.
Work to improve the characterization of the distribution of new and young sea ice types and open water amount within Arctic coastal polynyas through the combined use of ERS-1 SAR (Synthetic Aperture Radar) and DMSP SSM/I (Defense Meteorological Satellite Program Special Sensor Microwave/Imager) data is described. Two St. Lawrence Island polynya events are studied using low resolution, geocoded SAR images and coincident SSM/I data. The SAR images are analyzed in terms of polarization and spectral gradient ratios. Results of the combined analysis show that the SAR ice type classification is consistent with that from SSM/I and that the combined use of SAR and SSM/I can improve the characterization of thin ice better than either data set can do alone.
We have determined the vertical distribution of chlorine monoxide (ClO), from measurements of pressure-broadened molecular-emission spectra made over Thule, Greenland, during the 1993 Arctic spring. The measurements show a weak lower stratospheric layer of chlorine monoxide inside the vortex in late February, which was, however, significantly greater in mixing ratio than that seen in observations we made in the spring of 1992. ClO was also observed in much smaller quantities in early to mid-March 1993 when Thule was outside the vortex. The amount of ClO within the vortex was severely reduced by the time it returned over Thule in late March. This reduction occurred several weeks earlier relative to the winter solstice than the decline of ClO inside the Antarctic vortex in 1993. The enhanced Arctic lower stratospheric layer seen in late February 1993 at a nearly equivalent photochemical period, and beyond. We have calculated daily ozone loss rates, due primarily to the dimer chlorine catalytic cycle, from both sets of measurements. The vertical integral of the Arctic daily percentage ozone loss when the largest ClO levels were present, at the end of February, is found to be approximately one quarter of that in the Antarctic at a photochemical period only 1 week later. The relative weakness of daily ozone depletion, combined with the early disappearance of ClO in the Arctic, suggests that hemispheric dilution by ozone-poor air from within the Arctic vortex is unlikely to be sufficient to explain the historically extreme loss of midlatitude northern hemisphere ozone which began in 1992 and persisted throughout 1993.
Actinometric observations of radiation climate of central arctic
A synthetic aperture imaging L-band radar flown aboard the NASA CV-990 remotely sensed a number of ice-covered lakes about 48 km northwest of Bethel, Alaska. The image obtained is a high resolution, two-dimensional representation of the surface backscatter cross section, and large differences in backscatter returns are observed: homogeneous low returns, homogeneous high returns and/or low returns near lake borders, and high returns from central areas. It is suggested that a low return indicates that the lake is frozen completely to the bottom, while a high return indicates the presence of fresh water between the ice cover and the lake bed.
We present box model calculations of ozone loss rates corresponding to the results of the Match experiment 1991/92.
The Earth's northern hemisphere lower stratosphere was unusually cold in December 1995 and January 1995. Temperatures low enough for polar stratospheric cloud formation persisted until mid-March 1995, and the polar vortex was exceptionally strong throughout the winter. Previous and current Atmosphere Research Satellite (UARS) Microwave Limb Sounder (MLS) measurements indicating ozone depletion are given.
This paper discusses in situ measurements of O3, aerosol number density, and aerosol size obtained during NASA Arctic Boundary Layer Expedition aircraft flights over the Alaskan Arctic region. The major source of summer O3 for the troposphere in the intrusion of stratospheric air and subsequent transport to lower altitudes. Photochemistry of mixed layer emissions and O3 transported from high northern latitude urban/industrialized areas do not appear to play major roles as sources of O3 for the Alaska region. O3 gradients reflect the loss at the surface and supply from the stratosphere. Free tropospheric O3 averaged 74 ppbv compared to 32 ppbv for the mixed layer. O3 loss mechanisms are a combination of the destruction via photochemistry, chemical reaction with surface emissions, and direct loss through deposition to the surface. The boreal forest in the most efficient of the O3 sinks and has the largest increase in aerosol number density relative to the free troposphere.
Observations taken over the last few decades indicate that dramatic changes are occurring in the ArcticBoreal Zone (ABZ), which are having significant impacts on ABZ inhabitants, infrastructure, flora and fauna, and economies. While suitable for detecting overall change, the current capability is inadequate for systematic monitoring and for improving process based and large scale understanding of the integrated components of the ABZ, which includes the cryosphere, biosphere, hydrosphere, and atmosphere. Such knowledge will lead to improvements in Earth system models, enabling more accurate prediction of future changes and development of informed adaptation and mitigation strategies. In this article, we review the strengths and limitations of current space based observational capabilities for several important ABZ components and make recommendations for improving upon these current capabilities. We recommend an interdisciplinary and stepwise approach to develop a comprehensive ABZ Observing Network (ABZON), beginning with an initial focus on observing networks designed to gain process based understanding for individual ABZ components and systems that can then serve as the building blocks for a comprehensive ABZON.
Observations taken over the last few decades indicate that dramatic changes are occurring in the ArcticBoreal Zone (ABZ), which are having significant impacts on ABZ inhabitants, infrastructure, flora and fauna, and economies. While suitable for detecting overall change, the current capability is inadequate for systematic monitoring and for improving processbased and largescale understanding of the integrated components of the ABZ, which includes the cryosphere, biosphere, hydrosphere, and atmosphere. Such knowledge will lead to improvements in Earth system models, enabling more accurate prediction of future changes and development of informed adaptation and mitigation strategies. In Duncan et al. (2020), we review the strengths and limitations of current spacebased observational capabilities for several important ABZ components and make recommendations for improving upon these current capabilities. We recommend an interdisciplinary and stepwise approach to develop a comprehensive ABZ Observing Network (ABZON), beginning with an initial focus on observing networks designed to gain processbased understanding for individual ABZ components and systems that can then serve as the building blocks for a comprehensive ABZON.