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At least 361 records · Page 20
All sourcesNASA NTRSDOE OSTI
NASA NTRS1990

Arctic multiyear ice classification and summer ice cover using passive microwave satellite data

Passive microwave data collected by Nimbus 7 were used to classify and monitor the Arctic multilayer sea ice cover. Sea ice concentration maps during several summer minima are analyzed to obtain estimates of ice floes that survived summer, and the results are compared with multiyear-ice concentrations derived from these data by using an algorithm that assumes a certain emissivity for multiyear ice. The multiyear ice cover inferred from the winter data was found to be about 25 to 40 percent less than the summer ice-cover minimum, indicating that the multiyear ice cover in winter is inadequately represented by the passive microwave winter data and that a significant fraction of the Arctic multiyear ice floes exhibits a first-year ice signature.

Comiso, J. C.↗
NASA NTRS1990

Ozone loss in the Arctic polar vortex inferred from high-altitude aircraft measurements

The Arctic polar vortex in winter is known to be chemically primed for ozone depletion, yet it does not exhibit the large seasonal ozone decrease that characterizes its southern counterpart. This difference may be due in part to a net flux of ozone-rich air through the Arctic vortex, which can mask ozone loss. But by using a chemically conserved tracer as a reference, significant ozone loss can be identified. This loss is found to be correlated with high levels of chlorine monoxide, suggesting that much of the decrease in ozone is caused by anthropogenic emissions of chlorofluorocarbons.

Proffitt, M. H.↗
NASA NTRS1991

Airborne lidar measurements of ozone during the 1989 airborne Arctic stratospheric expedition

The NASA/NOAA Airborne Arctic Stratospheric Expedition (AASE) was conducted during the winter to study the conditions leading to possible ozone (O3) destruction in the wintertime Arctic stratosphere. As part of this experiment, the NASA-Langley airborne differential absorption lidar (DIAL) system was configured for operation on the NASA-Ames DS-8 aircraft to make measurements of O3 profiles from about 1 km above the aircraft to altitudes of 22 to 26 km. The airborne DIAL system remotely sensed O3 above the DC-8 by transmitting two laser beams at 10 Hz using wavelengths of 301.5 and 311 nm. Large scale distributions of O3 were obtained on 15 long range flights into the polar vortex during the AASE. Selected data samples are presented of O3 observed during these flights, general trends observed in O3 distributions, and correlations between these measurements and meteorological and chemical parameters. The O3 distribution observed on the first flight of the DC-8 into the polar vortex on Jan. 6 reflected the result of diabatic cooling of the air inside the vortex during the winter compared to the warmer air outside the vortex. On a potential temperature surface, the O3 mixing ratio generally increases when going from outside to inside the vortex.

Browell, Edward V.↗
NASA NTRS1990

Arctic contribution to upper-ocean variability in the North Atlantic

The potential climatic leverage of salinity and temperature anomalies in the high-latitude North Atlantic is large. Substantial variations of sea ice have accompanied North Atlantic salinity and temperature anomalies. Atmospheric pressure data are used here to show that the local forcing of high-latitude North Atlantic Ocean fluctuations is augmented by antecedent atmospheric circulation anomalies over the central Arctic. These circulation anomalies are consistent with enhanced wind-forcing of thicker older ice into the Transpolar Drift Stream and an enhanced export of sea ice (fresh water) from the Arctic into the Greenland Sea prior to major episodes of ice severity in the Greenland and Iceland seas.

Walsh, John E.↗
NASA NTRS1991

The potential for ozone depletion in the Arctic polar stratosphere

The nature of the Arctic polar stratosphere is observed to be similar in many respects to that of the Antarctic polar stratosphere, where an ozone hole has been identified. Most of the available chlorine (CHl and ClONO2) was converted by reactions on polar stratospheric clouds to reactive ClO and Cl2O2 thoroughout the Arctic polar vortex before midwinter. Reactive nitrogen was converted to HNO3, and some, with spatial inhomogeneity, fell out of the stratosphere. These chemical changes ensured characteristic ozone losses of 10 to 15 percent at altitudes inside the polar vortex where polar stratospheric clouds had occurred. These local losses can translate into 5 to 8 percent losses in the vertical column abundance of ozone. As the amount of stratospheric chlorine inevitably increases by 50 percent over the next two decades, ozone losses recognizable as an ozone hole may well appear.

Brune, W. H.↗
NASA NTRS1991

Recent variations in Arctic and Antarctic sea-ice covers

Variations in the extents of sea-ice cover at the poles and the areas of open water enclosed within them were observed every other day during the interval 1978-1987 by a satellite-borne scanning multispectral microwave radiometer. A band-limited regression technique shows that the trends in coverage of the Arctic and Antarctic sea-ice packs are not the same. During these nine years, there are significant decreases in ice extent and open-water areas within the ice cover in the Arctic, whereas in the Antarctic, there are no significant trends.

Gloersen, Per↗
NASA NTRS1992

Lidar Atmospheric Observatory in the Canadian Arctic

During the last decade there have been growing concerns about a broad variety of atmospheric properties. Among these, a depletion of the stratospheric ozone layer has attracted considerable attention from the general public, politicians and scientists due to its vital impact for the entire global biosphere. One of the major warning signs was the discovery of the 'ozone hole' in the Antarctic region where the concentration of the ozone in the stratosphere was significantly reduced. At present the stratospheric ozone layer in this region is being continuously monitored by groups of scientists from around the world and numerous observations of the ozone layer on the global scale have clearly demonstrated the process of ozone depletion. Recent observations by NASA have shown significant depletion in the Arctic region. This paper provides an initial description of two lidars that are planned to be installed in a new observatory for atmospheric studies in the Canadian Arctic. This observatory is being constructed under the supervision of the Atmospheric Environment Services (AES) of Canada as a part of Green Plan - an initiative of the Federal Government of Canada. The station is located at Eureka on Ellesmere Island at a latitude of 80 degrees N and a longitude of 86 degrees W.

Ulitsky, Arkady↗
NASA NTRS1992

Airborne Lidar Measurements of Stratospheric Aerosols During the European Arctic Stratospheric Ozone Experiment (EASOE)

The European Arctic Statospheric Ozone Experiment was performed during the winter of 1991/1992 to study processes in the Arctic Stratosphere, which possibly might result in an ozone depletion similar to what has been found in the Antarctic. Besides a number of ground observations at several locations and numerous balloon borne in situ and remote sensing experiments, three aircrafts were operating from the airport of Kiruna, Sweden, two of them equipped with lidars. Various aspects of this investigation are presented.

Renger, Wolfgang↗
NASA NTRS1992

Composition measurements of the 1989 Arctic winter stratosphere by airborne infrared solar absorption spectroscopy

The paper reports simultaneous measurements of the stratospheric burdens of H2O, HDO, OCS, CO2, O3, N2O, CO, CH4, CF2Cl2, CFCl3, CHF2Cl, C2H6, HCN, NO, NO2, HNO3, ClNO3, HOCl, HCl, and HF made by the JPL MkIV interferometer on board the NASA DC-8 aircraft during January and early February 1989 as part of the Airborne Arctic Stratosphere Experiment. Data were obtained on 11 flights at altitudes of up to 12 km over a geographic region covering the NE Atlantic Ocean, Iceland, and Greenland. Analyses of the chemically active gases reveal highly perturbed conditions within the vortex. The ClNO3 abundance was chemically enhanced near the edge of the vortex but was then depleted inside. NO2 was severely depleted inside the vortex. In contrast to Antarctica, H2O and HNO3 were both more abundant inside the vortex than outside. It is suggested that although the Arctic vortex did not get cold enough to produce any dehydration, or as vertically extensive denitrification as occurred in Antarctica, nevertheless, enough heterogeneous chemistry occurred to convert over 90 percent of the inorganic chlorine to active forms in the 14- to 27-km altitude range by early February 1989.

Toon, G. C.↗
NASA NTRS1992

Particle size distributions in Arctic polar stratospheric clouds, growth and freezing of sulfuric acid droplets, and implications for cloud formation

The paper uses particle size and volume measurements obtained with the forward scattering spectrometer probe model 300 during January and February 1989 in the Airborne Arctic Stratospheric Experiment to investigate processes important in the formation and growth of polar stratospheric cloud (PSC) particles. It is suggested on the basis of comparisons of the observations with expected sulfuric acid droplet deliquescence that in the Arctic a major fraction of the sulfuric acid droplets remain liquid until temperatures at least as low as 193 K. It is proposed that homogeneous freezing of the sulfuric acid droplets might occur near 190 K and might play a role in the formation of PSCs.

Dye, James E.↗
NASA NTRS1993

Radar backscatter measurements from Arctic sea ice during the fall freeze-up

Radar backscatter measurements from sea ice during the fall freeze-up were performed by the United States Coast Guard Icebreaker Polar Star as a part of the International Arctic Ocean Expedition (IAOE'91) from Aug. to Sep. 1991. The U.S. portion of the experiment took place on board the Polar Star and was referred to as TRAPOLEX '91 (Transpolar expedition) by some investigators. Before prematurely aborting its mission because of mechanical failure of her port shaft, the Polar Star reached 84 deg 57 min N latitude at 35 deg E longitude. The ship was in the ice (greater than 50 percent coverage) from 14 Aug. until 3 Sep. and was operational for all but 6 days due to two instances of mechanical problems with the port shaft. The second was fatal to the ship's participation in the expedition. During the expedition, radar backscatter was measured at C-band under a variety of conditions. These included measurements from young ice types as well as from multiyear and first-/second-year sea ice during the fall freeze-up. The sea ice types were determined by measurement of the ice properties at several of the stations and by visual inspection on others. Radar backscatter measurements were performed over a large portion of the ship's transit into the Arctic ice pack. These were accompanied by in situ sea ice property characterization by the U.S. Army Cold Regions Research and Engineering Laboratory (CRREL) at several stations and, when snow was present, its properties were documented by The Microwave Group, Ottawa River (MWG).

Beaven, S.↗
NASA NTRS1992

Tropospheric ozone and aerosol observations - The Alaskan Arctic

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.

Gregory, Gerald L.↗
NASA NTRS1992

Soluble species in the Arctic summer troposphere - Acidic gases, aerosols, and precipitation

The large-scale spatial distribution from 0.15-to 6 km altitude in the North American Arctic troposphere of several soluble acidic gases and major aerosol species during the summertime is reported. The distribution is found to be compositionally consistent on a large spatial scale. The summertime troposphere is an acidic environment, with HCOOH and CH3COOH the principal acidic gases while acidic sulfate aerosols dominate the particulate phase. There appears to be a surface source of NH3 over the pack ice which may originate from decay of dead marine organisms on the ice surface, evolution from surface ocean waters in open ice leads, or release from rotting sea ice. At low altitude over the pack ice this NH34 appears to partially neutralize aerosol acidity. Over sub-Arctic tundra in southeastern Alaska, inputs of marine biogenic sulfur from the Bering Sea appear to be an important source of boundary layer aerosol SO4(2-). The rainwater acidity over the tundra is typical of remote regions.

Talbot, R. W.↗
NASA NTRS1992

Methane emissions from Alaska Arctic tundra - An assessment of local spatial variability

The findings of an extensive midsummer survey of CH4 emissions measurements representing the Alaska Arctic tundra are presented. Variability in rates of emissions was similar in magnitude on local and regional scales, ranging from 0 to 286.5 mg/sq m/d overall and often varying across two orders of magnitude within 0.5 m distances. Primary control on rates of emission was determined by the substrate and position of the water table relative to the surface. Emission rates in the Arctic Foothills ranged from 0.2 mg/sq m/d for tussock tundra to 55.53 mg/sq m/d over wet meadows. Plant-mediated release of CH4 to the atmosphere was directly proportional to green leaf area and represented 92-98 percent of the total emission rates over vegetated sites. The results suggest the current published emission rates may have overestimated the contribution of boreal ecosystems to the global CH4 budget by several fold.

Morrissey, L. A.↗
NASA NTRS1992

Relationship between sea ice freeboard and draft in the Arctic Basin, and implications for ice thickness monitoring

This study confirms the finding of Comiso et al. (1991) that the probability density function (pdf) of the ice freeboard in the Arctic Ocean can be converted to a pdf of ice draft by applying a simple coordinate factor. The coordinate factor, R, which is the ratio of mean draft to mean freeboard pdf is related to the mean material (ice plus snow) density, rho(m), and the near-surface water density rho(w) by the relationship R = rho(m)/(rho(w) - rho(m)). The measured value of R was applied to each of six 50-km sections north of Greenland of a joint airborne laser and submarine sonar profile obtained along nearly coincident tracks from the Arctic Basin north of Greenland and was found to be consistent over all sections tested, despite differences in the ice regime. This indicates that a single value of R might be used for measurements done in this season of the year. The mean value R from all six sections was found to be 7.89.

Wadhams, P.↗
NASA NTRS1991

Airborne lidar measurements of ozone and aerosols in the summertime Arctic troposphere

Ozone (O3) and aerosol distributions were remotely measured from an aircraft using a differential absorption lidar (DIAL) system as part of the 1988 NASA Global Tropospheric Experiment - Arctic Boundary Layer Experiment (ABLE-3A). The airborne DIAL system made simultaneous measurements of O3 and aerosols from the surface to above the tropopause. These measurements were made in a broad range of atmospheric conditions over the tundra, ice, and ocean regions near Barrow and Bethel, Alaska, during July and August 1988. The tropospheric composition over the Arctic was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were usually correlated with descending air from the upper troposphere or lower stratosphere. Several cases of enhanced O3 were observed during ABLE-3A in conjunction with enhanced aerosol layers in the free troposphere resulting from biomass burning. As was found in the Amazon, the products of biomass burning can significantly alter O3 concentrations in the troposphere. This paper describes the NASA airborne DIAL system and discusses the large-scale variations of O3 and aerosols observed with the airborne DIAL system during ABLE-3A.

Browell, Edward V.↗
NASA NTRS1993

Summer Arctic ice concentrations and characteristics from SAR and SSM/I data

The extent and concentration of the Summer minima provide indirect information about the long term ability of the perennial portion of the ice pack to survive the Arctic atmosphere and ocean system. Both active and passive microwave data were used with some success for monitoring the ice cover during the Summer, but they both suffer from similar problems caused by the presence of meltponding, surface wetness, flooding, and freeze/thaw cycles associated with periodic changes in surface air temperatures. A comparative analysis of ice conditions in the Arctic region using coregistered ERS-1 SAR (Synthetic Aperture Radar) and SSM/I (Special Sensor Microwave/Imager) data was made. The analysis benefits from complementary information from the two systems, the good spatial resolution of SAR data, and the good time resolution of and global coverage by SSM/I data. The results show that in many areas ice concentrations derived from SAR data are significantly different (usually higher) than those derived from passive microwave data. Additional insights about surface conditions can be inferred depending on the nature of the discrepancies.

Comiso, Joey C.↗
NASA NTRS1993

Chemical loss of ozone in the Arctic polar vortex in the winter of 1991- 1992

In situ measurements of chlorine monoxide, bromine monoxide, and ozone are extrapolated globally, with the use of meteorological tracers, to infer the loss rates for ozone in the Arctic lower stratosphere during the Airborne Arctic Stratospheric Expedition II (AASE II) in the winter of 1991-1992. The analysis indicates removal of 15 to 20 percent of ambient ozone because of elevated concentrations of chlorine monoxide and bromine monoxide. Observations during AASE II define rates of removal of chlorine monoxide attributable to reaction with nitrogen dioxide (produced by photolysis of nitric acid) and to production of hydrochloric acid. Ozone loss ceased in March as concentrations of chlorine monoxide declined. Ozone losses could approach 50 percent if regeneration of nitrogen dioxide were inhibited by irreversible removal of nitrogen oxides (denitrification), as presently observed in the Antarctic, or without denitrification if inorganic chlorine concentrations were to double.

Salawitch, R. J.↗