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1.
Ozone is an important observable tracer of martian photochemistry, including odd hydrogen (HOx) species important to the chemistry and stability of the martian atmosphere. Infrared heterodyne spectroscopy with spectral resolution ?106 provides the only ground-based direct access to ozone absorption features in the martian atmosphere. Ozone abundances were measured with the Goddard Infrared Heterodyne Spectrometer and the Heterodyne Instrument for Planetary Wind and Composition at the NASA Infrared Telescope Facility on Mauna Kea, Hawai'i. Retrieved total ozone column abundances from various latitudes and orbital positions (LS=40°, 74°, 102°, 115°, 202°, 208°, 291°) are compared to those predicted by the first three-dimensional gas phase photochemical model of the martian atmosphere [Lefèvre, F., Lebonnois, S., Montmessin, F., Forget, F., 2004. J. Geophys. Res. 109, doi:10.1029/2004JE002268. E07004]. Observed and modeled ozone abundances show good agreement at all latitudes at perihelion orbital positions (LS=202°, 208°, 291°). Observed low-latitude ozone abundances are significantly higher than those predicted by the model at aphelion orbital positions (LS=40°, 74°, 115°). Heterogeneous loss of odd hydrogen onto water ice cloud particles would explain the discrepancy, as clouds are observed at low latitudes around aphelion on Mars.  相似文献   

2.
Hydrogen peroxide (H2O2) has been suggested as a possible oxidizer of the martian surface. Photochemical models predict a mean column density in the range of 1015-1016 cm−2. However, a stringent upper limit of the H2O2 abundance on Mars (9×1014 cm−2) was derived in February 2001 from ground-based infrared spectroscopy, at a time corresponding to a maximum water vapor abundance in the northern summer (30 pr. μm, Ls=112°). Here we report the detection of H2O2 on Mars in June 2003, and its mapping over the martian disk using the same technique, during the southern spring (Ls=206°) when the global water vapor abundance was ∼10 pr. μm. The spatial distribution of H2O2 shows a maximum in the morning around the sub-solar latitude. The mean H2O2 column density (6×1015 cm−2) is significantly greater than our previous upper limit, pointing to seasonal variations. Our new result is globally consistent with the predictions of photochemical models, and also with submillimeter ground-based measurements obtained in September 2003 (Ls=254°), averaged over the martian disk (Clancy et al., 2004, Icarus 168, 116-121).  相似文献   

3.
Michael D Smith 《Icarus》2004,167(1):148-165
We use infrared spectra returned by the Mars Global Surveyor Thermal Emission Spectrometer (TES) to retrieve atmospheric and surface temperature, dust and water ice aerosol optical depth, and water vapor column abundance. The data presented here span more than two martian years (Mars Year 24, Ls=104°, 1 March 1999 to Mars Year 26, Ls=180°, 4 May 2003). We present an overview of the seasonal (Ls), latitudinal, and longitudinal dependence of atmospheric quantities during this period, as well as an initial assessment of the interannual variability in the current martian climate. We find that the perihelion season (Ls=180°-360°) is relatively warm, dusty, free of water ice clouds, and shows a relatively high degree of interannual variability in dust optical depth and atmospheric temperature. On the other hand, the aphelion season (Ls=0°-180°) is relatively cool, cloudy, free of dust, and shows a low degree of interannual variability. Water vapor abundance shows a moderate amount of interannual variability at all seasons, but the most in the perihelion season. Much of the small amount of interannual variability that is observed in the aphelion season appears to be caused by perihelion-season planet-encircling dust storms. These dust storms increase albedo through deposition of bright dust on the surface causing cooler daytime surface and atmospheric temperatures well after dust optical depth returns to prestorm values.  相似文献   

4.
There is a significant progress in the observational data relevant to Mars photochemistry in the current decade. These data are not covered by and sometimes disagree with the published models. Therefore we consider three types of models for Mars photochemistry. A steady-state model for global-mean conditions is currently the only way to calculate the abundances of long living species (H2, O2, and CO). However, our model does not fit the observed CO abundance using gas-phase chemistry and reasonable values of heterogeneous loss of odd hydrogen on the water ice aerosol. The second type of the calculated models is steady-state models for local conditions. The MGS/TES data on temperature profiles, H2O, and dust are input parameters for these models. The calculations have been made for nine seasonal points spread over the martian year and for twelve latitudes with a step of 10° for each season. The only adopted heterogeneous reaction is a weak loss of H2O2 on water ice with probability of 5×10−4. The results are in good agreement with the recent observations of the O2 dayglow at 1.27 μm and the O3 and H2O2 abundances. Global maps of the seasonal and latitudinal behavior of these species have been made. The third type of models is a time-dependent model for local conditions. These models show that odd hydrogen quickly converts to H2O2 at the nighttime and the chemistry is switched off while the association of O, the heterogeneous loss of H2O2, and eddy diffusion continue. This requires significant changes in the global-mean and local steady-state models discussed above, and these changes have been properly done. The calculated diurnal variations of Mars photochemistry are discussed. The martian photochemistry at low and middle latitudes is significantly different in the aphelion period at LS=10°-130° from that in the remaining part of the year.  相似文献   

5.
Atmospheric water vapor abundances in Mars’ north polar region (NPR, from 60° to 90°N) are mapped as function of latitude and longitude for spring and summer seasons, and their spatial, seasonal, and interannual variability is discussed. Water vapor data are from Mars Global Surveyor (MGS) Thermal Emission Spectrometer (TES) and the Viking Orbiter (VO) Mars Atmospheric Water Detector (MAWD). The data cover three complete northern spring-summer seasons in 1977-1978, 2000-2001 and 2002-2003, and shorter periods of spring-summer seasons during 1975, 1999 and 2004. Long term interannual variability in the averaged NPR abundances may exist, with Viking MAWD observations showing twice as much water vapor during summer as the MGS TES observations more than 10 martian years (MY) later. While the averaged abundances are very similar in TES observations for the same season in different years, the spatial distributions in the early summer season do vary significantly year over year. Spatial and temporal variabilities increase between Ls ∼ 80-140°, which may be related to vapor sublimation from the North Polar Residual Cap (NPRC), or to changes in circulation. Spatial variability is observed on scales of ∼100 km and temporal variability is observed on scales of <10 sols during summer. During late spring the TES water vapor spatial distribution is seen to correlate with the low topography/low albedo region of northern Acidalia Planitia (270-360°E), and with the dust spatial distribution across the NPR during late spring-early summer. Non-uniform vertical distribution of water vapor, a regolith source or atmospheric circulation ‘pooling’ of water vapor from the NPRC into the topographic depression may be behind the correlation with low topography/low albedo. Sublimation winds carrying water vapor off the NPRC and lifting surface dust in the areas surrounding the NPRC may explain the correlation between the water vapor and dust spatial distributions. Correlation between water vapor and dust in MAWD data are only observed over low topography/low albedo area. Maximum water vapor abundances are observed at Ls = 105-115° and outside of the NPRC at 75-80°N; the TES data, however, do not extend over the NPRC and thus, this conclusion may be biased. Some water vapor appears to be released in plumes or ‘outbursts’ in the MAWD and TES datasets during late spring and early summer. We propose that the sublimation rate of ice varies across the NPRC with varying surface winds, giving rise to the observed ‘outbursts’ at some seasons.  相似文献   

6.
New maps of martian water vapor and hydrogen peroxide have been obtained in November-December 2005, using the Texas Echelon Cross Echelle Spectrograph (TEXES) at the NASA Infra Red Telescope facility (IRTF) at Mauna Kea Observatory. The solar longitude Ls was 332° (end of southern summer). Data have been obtained at 1235-1243 cm−1, with a spectral resolution of 0.016 cm−1 (R=8×104). The mean water vapor mixing ratio in the region [0°-55° S; 345°-45° W], at the evening limb, is 150±50 ppm (corresponding to a column density of 8.3±2.8 pr-μm). The mean water vapor abundance derived from our measurements is in global overall agreement with the TES and Mars Express results, as well as the GCM models, however its spatial distribution looks different from the GCM predictions, with evidence for an enhancement at low latitudes toward the evening side. The inferred mean H2O2 abundance is 15±10 ppb, which is significantly lower than the June 2003 result [Encrenaz, T., Bézard, B., Greathouse, T.K., Richter, M.J., Lacy, J.H., Atreya, S.K., Wong, A.S., Lebonnois, S., Lefèvre, F., Forget, F., 2004. Icarus 170, 424-429] and lower than expected from the photochemical models, taking in account the change in season. Its spatial distribution shows some similarities with the map predicted by the GCM but the discrepancy in the H2O2 abundance remains to be understood and modeled.  相似文献   

7.
We present absolute abundances and latitudinal variations of ozone and water in the atmosphere of Mars during its late northern spring (Ls=67.3°) shortly before aphelion. Long-slit maps of the a1Δg state of molecular oxygen (O2) and HDO, an isotopic form of water, were acquired on UT January 21.6 1997 using a high-resolution infrared spectrometer (CSHELL) at the NASA Infrared Telescope Facility. O2(a1Δg) is produced by ozone photolysis, and the ensuing dayglow emission at 1.27 μm is used as a tracer for ozone. Retrieved vertical column densities for ozone above ∼20 km ranged between 1.5 and 2.8 μm-atm at mid- to low latitudes (30°S-60°N) and decreased outside that region. A significant decrease in ozone density is seen near 30°N (close to the subsolar latitude of 23.5°N). The rotational temperatures retrieved from O2(a-X) emissions show a mean of 172±2.5 K, confirming that the sensed ozone lies in the middle atmosphere (∼24 km). The ν1 fundamental band of HDO near 3.67 μm was used as a proxy for H2O. The retrieved vertical column abundance of water varies from 3 precipitable microns (pr-μm) at ∼30°S to 24 pr-μm at ∼60°N. We compare these results with current photochemical models and with measurements obtained by other methods.  相似文献   

8.
We report on new retrievals of water vapor column abundances from the Mars Global Surveyor (MGS) Thermal Emission Spectrometer (TES) data. The new retrievals are from the TES nadir data taken above the ‘cold’ surface areas in the North polar region (Tsurf < 220 K, including seasonal frost and permanent ice cap) during spring and summer seasons, where retrievals were not performed initially. Retrievals are possible (with some modifications to the original algorithm) over cold surfaces overlaid by sufficiently warm atmosphere. The retrieved water vapor column abundances are compared to the column abundances observed by other spacecrafts in the Northern polar region during spring and summer and good agreement is found. We detect an annulus of water vapor growing above the edge of the retreating seasonal cap during spring. The formation of the vapor annulus is consistent with the previously proposed mechanism for water cycling in the polar region, according to which vapor released by frost sublimation during spring re-condenses on the retreating seasonal CO2 cap. The source of the vapor in the vapor annulus, according to this model, is the water frost on the surface of the CO2 at the retreating edge of the cap and the frost on the ground that is exposed by the retreating cap. Small contribution from regolith sources is possible too, but cannot be quantified based on the TES vapor data alone. Water vapor annulus exhibits interannual variability, which we attribute to variations in the atmospheric temperature. We propose that during spring and summer the water ice sublimation is retarded by high relative humidity of the local atmosphere, and that higher atmospheric temperatures lead to higher vapor column abundances by increasing the water holding capacity of the atmosphere. Since the atmospheric temperatures are strongly influenced by the atmospheric dust content, local dust storms may be controlling the release of vapor into the polar atmosphere. Water vapor abundances above the residual polar cap also exhibit noticeable interannual variability. In some years abundances above the cap are lower than the abundances outside of the cap, consistent with previous observations, while in the other years the abundances above the cap are higher or similar to abundances outside of the cap. We speculate that the differences may be due to weaker off-cap transport in the latter case, keeping more vapor closer to the source at the surface of the residual cap. Despite the large observed variability in water vapor column abundances in the Northern polar region during spring and summer, the latitudinal distribution of the vapor mass in the atmosphere is very similar during the summer season. If the variability in vapor abundances is caused by the variability of vapor sources across the residual cap then this would mean that they annually contribute relatively little vapor mass to significantly affect the vapor mass budget. Alternatively this may suggest that the vapor variability is caused by the variability of the polar atmospheric circulation. The new water vapor retrievals should be useful in tuning the Global Circulation Models of the martian water cycle.  相似文献   

9.
Our ground-based measurements of martian atmospheric water vapor, made throughout Ls=34° to 249°, 24 September 1998 to 23 November 1999, during Mars year 24 (MY 24), show changes in Mars' humidity on hourly, daily, and seasonal timescales. We made concomitant measurement of nearby CO2 bands, and when possible, results were corrected for aerosol extinction using aerosol optical depths derived from our own CO2 analysis. Where there is spatial and temporal overlap, similar results are obtained for water vapor abundances and aerosol opacities as those observed from the Thermal Emission Spectrometer on Mars Global Surveyor. In addition some further discussion of our published earlier water vapor measurements (1991-1995) is included. Six results from this data set are: (1) the measured aerosol opacity in Mars atmosphere was variable but not greater than τ=1, with almost no clear atmosphere being observed, (2) measurements made with the slit crossing many hours of local time on Mars' Earth-facing disk show a diurnal pattern with highest abundances at mid-day and low abundance in very early morning and late afternoon for some but not all measurements, (3) water vapor abundance is patchy on hourly and daily time scales but follows the usual seasonal trends seen by instrumentation on the Mars Atmospheric Water Detector on the Viking Orbiters and by the Thermal Emission Spectrometer on Mars Global Surveyor, (4) there is a slight longitudinal correlation with the ground-ice observed by the Gamma Ray Spectrometer on Mars Odyssey, (5) there is evidence of the Low Southern Latitude Summer Minimum in our water vapor measurements but our data set for southern summer is limited, and (6) MY 24 appears to be wetter than MY 22 and MY 23.  相似文献   

10.
The O2 dayglow at 1.27 μm is formed by high-altitude ozone on Mars and is a sensitive tracer of Mars photochemistry. Mapping of this dayglow using the IRTF/CSHELL long-slit spectrograph requires the extraction of weak emission lines against a strong continuum of the reflected solar light. Some new tools are suggested to improve the data processing. The observed O2 dayglow intensities at LS=67°, 112°, 148°, and 173° show a decrease from late spring (aphelion) to fall equinox by a factor of ≈5 at low latitudes (±30°). This decrease agrees with that predicted by a model of Clancy and Nair (1996, J. Geophys. Res. 101 (12) 12785-12790), although the dayglow intensities are weaker than those based on that model. The measured dayglow variations with latitude are rather low at LS=67°, 112°, and 148° and unexpectedly high at 173°. The dayglow intensity peaks near noon and is smaller at 9:00 and 16:30 LT by a factor of 2. Some data on the ozone profile near aphelion are obtained from a combination of the dayglow and ozone observations. It is hardly possible to detect the O2 night airglow at 1.27 μm on Mars using the existing ground-based and on-orbit instruments. The O2 dayglow intensity as a function of latitude and season from aphelion to fall equinox has been obtained. Our goal is to extend this distribution to the full martian year and get a database for Mars photochemistry to complement the MGS/TES observations of water vapor, atmospheric temperature, and dust and ice aerosol.  相似文献   

11.
Ozone is a tracer of photochemistry in the atmosphere of Mars and an observable used to test predictions of photochemical models. We present a comparison of retrieved ozone abundances on Mars using ground-based infrared heterodyne measurements by NASA Goddard Space Flight Center’s Heterodyne Instrument for Planetary Wind And Composition (HIPWAC) and space-based Mars Express Spectroscopy for the Investigation of the Characteristics of the Atmosphere of Mars (SPICAM) ultraviolet measurements. Ozone retrievals from simultaneous measurements in February 2008 were very consistent (0.8 μm-atm), as were measurements made close in time (ranging from <1 to >8 μm-atm) during this period and during opportunities in October 2006 and February 2007. The consistency of retrievals from the two different observational techniques supports combining the measurements for testing photochemistry-coupled general circulation models and for investigating variability over the long-term between spacecraft missions. Quantitative comparison with ground-based measurements by NASA/GSFC’s Infrared Heterodyne Spectrometer (IRHS) in 1993 reveals 2-4 times more ozone at low latitudes than in 2008 at the same season, and such variability was not evident over the shorter period of the Mars Express mission. This variability may be due to cloud activity.  相似文献   

12.
High-resolution infrared imaging spectroscopy of Mars has been achieved at the NASA Infrared Telescope Facility (IRTF) on June 19-21, 2003, using the Texas Echelon Cross Echelle Spectrograph (TEXES). The areocentric longitude was 206°. Following the detection and mapping of hydrogen peroxide H2O2 [Encrenaz et al., 2004. Icarus 170, 424-429], we have derived, using the same data set, a map of the water vapor abundance. The results appear in good overall agreement with the TES results and with the predictions of the Global Circulation Model (GCM) developed at the Laboratory of Dynamical Meteorology (LMD), with a maximum abundance of water vapor of 3±1.5×10−4(17±9 pr-μm). We have searched for CH4 over the martian disk, but were unable to detect it. Our upper limits are consistent with earlier reports on the methane abundance on Mars. Finally, we have obtained new measurements of CO2 isotopic ratios in Mars. As compared to the terrestrial values, these values are: (18O/17O)[M/E] = 1.03 ± 0.09; (13C/12C)[M/E] = 1.00 ± 0.11. In conclusion, in contrast with the analysis of Krasnopolsky et al. [1996. Icarus 124, 553-568], we conclude that the derived martian isotopic ratios do not show evidence for a departure from their terrestrial values.  相似文献   

13.
The infrared AOTF spectrometer is a part of the SPICAM experiment onboard the Mars-Express ESA mission. The instrument has a capability of solar occultations and operates in the spectral range of 1-1.7 μm with a spectral resolution of ∼3.5 cm−1. We report results from 24 orbits obtained during MY28 at Ls 130°-160°, and the latitude range of 40°-55° N. For these orbits the atmospheric density from 1.43 μm CO2 band, water vapor mixing ratio based on 1.38 μm absorption, and aerosol opacities were retrieved simultaneously. The vertical resolution of measurements is better than 3.5 km. Aerosol vertical extinction profiles were obtained at 10 wavelengths in the altitude range from 10 to 60 km. The interpretation using Mie scattering theory with adopted refraction indices of dust and H2O ice allows to retrieve particle size (reff∼0.5-1 μm) and number density (∼1 cm−3 at 15-30 km) profiles. The haze top is generally below 40 km, except the longitude range of 320°-50° E, where high-altitude clouds at 50-60 km were detected. Optical properties of these clouds are compatible with ice particles (effective radius reff=0.1-0.3 μm, number density N∼10 cm−3) distributed with variance νeff=0.1-0.2 μm. The vertical optical depth of the clouds is below 0.001 at 1 μm. The atmospheric density profiles are retrieved from CO2 band in the altitude range of 10-90 km, and H2O mixing ratio is determined at 15-50 km. Unless a supersaturation of the water vapor occurs in the martian atmosphere, the H2O mixing ratio indicates ∼5 K warmer atmosphere at 25-45 km than predicted by models.  相似文献   

14.
Measurements of martian atmospheric water vapor made throughout Ls = 18.0°-146.4° (October 3, 1996-July 12, 1997) show changes in Mars humidity on hourly, daily, and seasonal time scales. Because our observing program during the 1996-1997 Mars apparition did not include concomitant measurement of nearby CO2 bands, high northern latitude data were corrected for dust and aerosol extinction assuming an optical depth of 0.8, consistent with ground-based and HST imaging of northern dust storms. All other measurements with airmass greater than 3.5 were corrected using a total optical depth of 0.5. Three dominant results from this data set are as follows: (1) pre- and post-opposition measurements made with the slit crossing many hours of local time on Mars’ Earth-facing disk show a distinct diurnal pattern with highest abundances around and slightly after noon with low abundances in the late afternoon, (2) measurements of water vapor over the Mars Pathfinder landing site (Carl Sagan Memorial Station) on July 12, 1997, found 21 ppt μm in the spatial sector centered near 19° latitude, 36° longitude while abundances around the site varied from as low as 6 to as high as 28 ppt μm, and (3) water vapor abundance is patchy on hourly and daily time scales but follows the usual seasonal trends.  相似文献   

15.
Xun Zhu  Jeng-Hwa Yee 《Icarus》2007,189(1):136-150
A one-dimensional photochemical-transport model for the martian lower atmosphere has been developed to study the diurnal cycles of wave-photochemistry coupling. The model self-consistently calculates water vapor mixing ratio profiles, which exhibit strong vertical and diurnal variations mainly due to the high sensitivity of the saturation vapor pressure to temperature variation. The dynamical coupling of water vapor caused by the temperature variation induced by tidal waves, vertical transport parameterized by eddy diffusion, and linear relaxation introduced in condensation-sublimation processes all have similar timescales of diurnal variation. This leads to a significant asymmetric distribution of water vapor concentration as a function of local time. As a result, the net effect of the temperature variation by tidal waves depletes the water vapor concentration in its diurnal mean. The coupling processes also deplete the diurnally averaged HOx concentration, which in turn leads to significant enhancements of both ozone concentration and the associated airglow emissions in the martian atmosphere. The model also shows explicitly the importance of photochemical-transport coupling to the airglow emissions and its implications in species retrievals when the photochemical times of the excited states are comparable to the timescale of diurnal variation.  相似文献   

16.
Encouraged by recent results of the Mars Odyssey spacecraft mission and the OMEGA team (Mars Express) concerning water in equatorial latitudes between ±45° on Mars and the possible existence of hydrated minerals, we have investigated the water sorption properties of natural zeolites and clay minerals close to martian atmospheric surface conditions as well as the properties of Mg-sulfates and gypsum. To quantify the stability of hydrous minerals on the martian surface and their interaction with the martian atmosphere, the water adsorption and desorption properties of nontronite, montmorillonite, chabazite and clinoptilolite have been investigated using adsorption isotherms at low equilibrium water vapor pressures and temperatures, modeling of the adsorption equilibrium data, thermogravimetry (TG), differential scanning calorimetry (DSC), and proton magic angle spinning nuclear magnetic resonance measurements (1H MAS NMR). Mg-sulfate hydrates were also analyzed using TG/DSC methods to compare with clay mineral and zeolites. Our data show that these microporous minerals can remain hydrated under present martian atmospheric conditions and hold up to 2.5-25 wt% of water in their void volumes at a partial water vapor pressure of 0.001 mbar in a temperature range of 333-193 K. Results of the 1H MAS NMR measurements suggest that parts of the adsorbed water are liquid-like water and that the mobility of the adsorbed water might be of importance for adsorption-water-triggered chemistry and hypothetical exobiological activity on Mars.  相似文献   

17.
Up to now, there has been no corroboration from Cassini CIRS of the Voyager IRIS-discovery of cyanoacetylene (HC3N) ice in Titan’s thermal infrared spectrum. We report the first compelling spectral evidence from CIRS for the ν6 HC3N ice feature at 506 cm−1 at latitudes 62°N and 70°N, from which we derive particle sizes and column abundances in Titan’s lower stratosphere. We find mean particle radii of 3.0 μm and 2.3 μm for condensed HC3N at 62°N and 70°N, respectively, and corresponding ice phase molecular column abundances in the range 1-10 × 1016 mol cm−2. Only upper limits for cloud abundances can be established at latitudes of 85°N, 55°N, 30°N, 10°N, and 15°S. Under the assumption that cloud tops coincide with the uppermost levels at which HC3N vapor saturates, we infer geometric thicknesses for the clouds equivalent to 10-20 km or so, with tops at 165 km and 150 km at 70°N and 62°N, respectively.  相似文献   

18.
Mars was observed near the peak of the strongest SO2 band at 1364-1373 cm−1 with resolving power of 77,000 using the Texas Echelon Cross Echelle Spectrograph on the NASA Infrared Telescope Facility. The observation covered the Tharsis volcano region which may be preferable to search for SO2. The spectrum shows absorption lines of three CO2 isotopomers and three H2O isotopomers. The water vapor abundance derived from the HDO lines assuming D/H = 5.5 times the terrestrial value is 12±1.0 pr. μm, in agreement with the simultaneous MGS/TES observations of 14 pr. μm at the latitudes (50° S to 10° N) of our observation. Summing of spectral intervals at the expected positions of sixteen SO2 lines puts a 2σ upper limit on SO2 of 1 ppb. SO2 may be emitted into the martian atmosphere by seepage and is removed by three-body reactions with OH and O. The SO2 lifetime, 2 years, is longer than the global mixing time 0.5 year, so SO2 should be rather uniformly distributed across Mars. Seepage of SO2 is less than 15,000 tons per year on Mars which is smaller than the volcanic production of SO2 on the Earth by a factor of 700. Because CH4/SO2 is typically 10−4-10−3 in volcanic gases on the Earth, our results show seepage is unlikely to be the source of the recently discovered methane on Mars and therefore strengthen its biogenic origin.  相似文献   

19.
We used MGS-MOC and MRO-MARCI daily mapping images of the North Polar Region of Mars from 16 August 2005 (Ls = 270°) to 21 May 2009 (Ls = 270°), covering portions of three consecutive martian years (MY 27-MY 29), to observe the seasonal behavior of the polar ice cap and atmospheric phenomena. The rate of cap regression was similar in MY 28 and MY 29, but was advanced by 3.5° of Ls (∼7-8 sols) in MY 29. The spatial and temporal behaviors of dust and condensate clouds were similar in the two years and generally in accord with prior years. Dust storms (>100 km2) were observed in all seasons, with peak activity occurring at Ls = 10-20° from 50°N to 70°N and at Ls = 135-140° from 70°N to 90°N. The most active quadrant was 0-90°W in MY 28, shifting to 180-270°W in MY 29. The majority of regional storms in both years developed in longitudes from 10°W to 60°W. During late summer the larger storms obscure the North Polar Region in a cloud of dust that transitions to north polar hood condensate clouds around autumnal equinox.Changes in the distribution of perennial ice deposits, especially in Olympia Planum, were observed between the 2 years, with the MY 29 ice distribution being the most extensive observed to date. Modeling suggests that the small, bright ice patches on the residual cap are not the result of slope or elevation effects. Rather we suggest that they are the result of local meteorological effects on ice deposition. The annual darkening and brightening of peripheral areas of the residual cap around summer solstice can be explained by the sublimation of a brighter frost layer revealing an underlying darker, ice rich layer that itself either sublimes to reveal brighter material below or acts as a cold trap, attracting condensation of water vapor that brightens the surface. An alternative explanation invokes transport and deposition of dust on the surface from the cap interior, and later removal of that dust. The decrease in cap albedo and accompanying increase in near surface atmospheric stability may be related to the annual minimum of polar storm activity near northern summer solstice.  相似文献   

20.
The Pioneer Venus Orbiter Infrared Radiometer and Venera 15 Fourier Transform Spectrometer observations of thermal emission from Venus' middle atmosphere between 10° S and 50° N have been independently re-analyzed using a common method to determine global maps of temperature, cloud optical depth, and water vapor abundance. The spectral regions observed include the strong 15 μm carbon dioxide band and the 45 μm fundamental rotational water band. The different spatial and spectral resolutions of the two instruments have necessitated the development of flexible analysis tools. New radiative transfer and retrieval models have been developed for this purpose based on correlated-k absorption tables calculated with up-to-date spectral line data. The common analysis of these two sets of observations has hence been possible for the first time. From the PV OIR observations, the cloud-top unit optical depth pressure showed a minimum of ∼110±10 mbars in the evening equatorial region and a maximum of ∼160±12 mbars in the morning mid-latitude regions. From the Venera 15 FTS spectra, the cloud-top pressure was found to increase from morning values of ∼120±10 to 200±30 mbars in the late afternoon/early evening region. The cloud-top water vapor abundances observed by the PV OIR instrument were found to fluctuate from 10±5 ppm at night up to 90±15 ppm in the equatorial cloud-top region shortly after the sub-solar point. The mean Venera 15 FTS water vapor abundances were found to be 12±5 ppm with only a slight enhancement over the equatorial latitude bands and no clear day-night distinction. The common analysis of these two sets of observations broadly validates previously published individual findings. The differences in the retrieved atmospheric state can no longer be attributed to radiative transfer modeling bias and suggest significant temporal variability in the middle atmosphere of Venus.  相似文献   

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