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1.
Seismic velocity changes and nonvolcanic tremor activity in the Parkfield area in California reveal that large earthquakes induce long-term perturbations of crustal properties in the San Andreas fault zone. The 2003 San Simeon and 2004 Parkfield earthquakes both reduced seismic velocities that were measured from correlations of the ambient seismic noise and induced an increased nonvolcanic tremor activity along the San Andreas fault. After the Parkfield earthquake, velocity reduction and nonvolcanic tremor activity remained elevated for more than 3 years and decayed over time, similarly to afterslip derived from GPS (Global Positioning System) measurements. These observations suggest that the seismic velocity changes are related to co-seismic damage in the shallow layers and to deep co-seismic stress change and postseismic stress relaxation within the San Andreas fault zone.  相似文献   

2.
A combination of experimental, molecular dynamics, and kinetics modeling studies is applied to a system of concentrated aqueous sodium chloride particles suspended in air at room temperature with ozone, irradiated at 254 nanometers to generate hydroxyl radicals. Measurements of the observed gaseous molecular chlorine product are explainable only if reactions at the air-water interface are dominant. Molecular dynamics simulations show the availability of substantial amounts of chloride ions for reaction at the interface, and quantum chemical calculations predict that in the gas phase chloride ions will strongly attract hydroxl radicals. Model extrapolation to the marine boundary layer yields daytime chlorine atom concentrations that are in good agreement with estimates based on field measurements of the decay of selected organics over the Southern Ocean and the North Atlantic. Thus, ion-enhanced interactions with gases at aqueous interfaces may play a more generalized and important role in the chemistry of concentrated inorganic salt solutions than was previously recognized.  相似文献   

3.
A large fraction of atmospheric aerosols are derived from organic compounds with various volatilities. A National Oceanic and Atmospheric Administration (NOAA) WP-3D research aircraft made airborne measurements of the gaseous and aerosol composition of air over the Deepwater Horizon (DWH) oil spill in the Gulf of Mexico that occurred from April to August 2010. A narrow plume of hydrocarbons was observed downwind of DWH that is attributed to the evaporation of fresh oil on the sea surface. A much wider plume with high concentrations of organic aerosol (>25 micrograms per cubic meter) was attributed to the formation of secondary organic aerosol (SOA) from unmeasured, less volatile hydrocarbons that were emitted from a wider area around DWH. These observations provide direct and compelling evidence for the importance of formation of SOA from less volatile hydrocarbons.  相似文献   

4.
Five flights of the U-2 aircraft with a filter sampler aboard were flown in the Mount St. Helens debris from 19 May to 17 June 1980. Sulfate concentrations as large as 216 times the expected background were observed. The enhancements of acid chloride vapor were considerably smaller, suggesting an insignificant increase of background values of hydrogen chloride once the plume is well mixed throughout the lower stratosphere.  相似文献   

5.
A frost point hygrometer designed for aircraft operation was included in the complement of instruments assembled for the NASA U-2 flights through the plume of Mount St. Helens. Measurements made on the 22 May flight showed the water vapor to be closely associated with the aerosol plume. The water vapor mixing ratio by mass in the plume was as high as 40 x 10(-6). This compares with values of 2 x 10(-6) to 3 x 10(-6) outside of the plume.  相似文献   

6.
Measurements in situ of the neutral composition and temperature of the thermosphere of Venus are being made with a quadrupole mass spectrometer on the Pioneer Venus orbiter. The presence of many gases, incluiding the major constituents CO(2), CO, N(2), O, and He has been confirmed. Carbon dioxide is the most abundant constituent at altitudes below about 155 kilometers in the terminator region. Above this altitude atomic oxygen is the major constituent, with O/CO(2) ratios in the upper atmosphere being greater than was commonly expected. Isotope ratios of O and C are close to terrestrial values. The temperature inferred from scale heights above 180 kilometers is about 400 K on the dayside near the evening terminator at a solar zenith angle of about 69 degrees . It decreases to about 230 K when the solar zenith angle is about 90 degrees .  相似文献   

7.
Measurements of excess Ar(36) + Ar(38) ( released mainly at 1200 degrees C) in magnetic concentrates of Pacific sediments and in a dense concentrate of Greenland dust agree within an order of magnitude with expected concentrations implanted by solar-flare ion streams of energy less than 10 Mev per atomic-mass unit. The agreement implies that more than 10 percent of each concentrate may be extraterrestrial, depending on size distribution and flare spectra. Rare-gas measurements on fine-grained dust can provide data on: solar-flare "paleo-ion" fluxes, energy spectra, and isotopic abundances; identification, mineralogy, and chemistry of interplanetary dust; influx rates to Earth and sedimentation rates of oceanic cores; and lunar-surface residence and mixing times.  相似文献   

8.
The global distribution of fluorocarbon-12 and fluorocarbon-11 is used to establish a relatively fast interhemispheric exchange rate of 1 to 1.2 years. Atmospheric residence times of 65 to 70 years for fluorocarbon-12 and 40 to 45 years for fluorocarbon-l1 best fit the observational data. These residence times rule out the possibility of any significant missing sinks that may prevent these fluorocarbons from entering the stratosphere. Atmospheric measurements of methyl chloroform support an 8-to 10-year residence time and suggest global average hydroxyl radical (HO) concentrations of 3 x 10(5) to 4 x 10(5) molecules per cubic centimeter. These are a factor of 5 lower than predicted by models. Additionally, methyl chloroform global distribution supports Southern Hemispheric HO levels that are a factor of 1.5 or more larger than the Northern Hemispheric values. The long residence time and the rapid growth of methyl chloroform cause it to be a potentially significant depleter of stratospheric ozone. The oceanic sink for atmospheric carbon tetrachloride is about half as important as the stratospheric sink. A major source of methyl chloride (3 x 10(12)grams per year), sufficient to account for nearly all the atmospheric methyl chloride, has been identified in the ocean.  相似文献   

9.
Data obtained from measurements of the stratospheric aerosol at Laramie, Wyoming (41 degrees N), indicate that the background or nonvolcanic stratospheric sulfuric acid aerosol mass at northern mid-latitudes has increased by about 5 +/- 2 percent per year during the past 10 years. Whether this increase is natural or anthropogenic could not be determined at this time because of inadequate information on sulfur sources, in particular, carbonyl sulfide, which is thought to be the dominant nonvolcanic source of stratospheric sulfuric acid vapor. An increase in stratospheric sulfate levels has important climatic implications as well as heterogeneous chemical effects that may alter the concentration of stratospheric ozone.  相似文献   

10.
An olivine nephelinite from the lower part of a thick alkalic ultrabasic and mafic sequence of volcanic rocks of the northeastern part of the Siberian flood basalt province (SFBP) yielded a (40)Ar/(39)Ar plateau age of 253.3 +/- 2.6 million years, distinctly older than the main tholeiitic pulse of the SFBP at 250.0 million years. Olivine phenocrysts of this rock showed (3)He/(4)He ratios up to 12.7 times the atmospheric ratio; these values suggest a lower mantle plume origin. The neodymium and strontium isotopes, rare earth element concentration patterns, and cerium/lead ratios of the associated rocks were also consistent with their derivation from a near-chondritic, primitive plume. Geochemical data from the 250-million-year-old volcanic rocks higher up in the sequence indicate interaction of this high-(3)He SFBP plume with a suboceanic-type upper mantle beneath Siberia.  相似文献   

11.
Results from the Pioneer Venus sounder probe neutral mass spectrometer indicate that there is no difference in the isotopic ratios of carbon and oxygen between Venus and Earth to within +/- 5 percent. The mixing ratio of nitrogen is 3.5(+3)(-2) percent with an isotopic ratio within 20 percent of that of Earth. The ratio of argon-36 to argon-40 is 85 percent, and the ratio of argon-38 to argon-36 is 20 percent. The mixing ratios of argon-36 and argon-40 are approximately 40 and 50 parts per million, respectively, with an error of about a factor of 2 (mainly toward a lesser amount) resulting from uncertainty in the response of the ion pump to rare gases. Hydrogen chloride cannot account for more than a few percent of the 36 mass peak, and therefore the large excess of primordial argon is a reasonable conclusion. The ratio of neon-20 to argon-36 of 0.5 +/- 0.3 is definitely terrestrial in character rather than solar. These results indicate that there is a large excess of all primordial noble gases on Venus relative to Earth. There appears to be a considerably higher abundance of sulfur compounds below 20 kilometers than in or above the main cloud layer. The 32 and 60 mass peaks show a sharp increase below 22 kilometers, indicating the possible production of sulfur and carbon oxysulfide (COS) at the expense of sulfur dioxide.  相似文献   

12.
Measurements of cloud condensation nuclei were made from small samples of stratospheric air taken from a U-2 aircraft at altitudes ranging from 13 to 19 kilometers. The measured concentrations of nuclei both in and outside the plume from the May and June 1980 eruptions of Mount St. Helens were higher than expected, ranging from about 100 to about 1000 per cubic centimeter active at 1 percent supersaturation.  相似文献   

13.
Gas measurements made in the stratospheric plume from the eruption of Mount St. Helens on 18 May 1980 were not consistent with a reported large injection of radon-222 into the atmosphere. No enrichment in the volatile element polonium was found in filter samples, and the ratio of polonium-210 to lead-210 was not different from background values. Data obtained with an experimental impactor, flown shortly after the eruption, showed an increase of 10(3) in the stratospheric number concentration of submicrometer sulfate particles compared to concentrations before the eruption.  相似文献   

14.
Chlorinated hydrocarbons in the Sargasso sea atmosphere and surface water   总被引：2，自引：0，他引：2  
Polychlorinated biphenyls (PCB), DDT, and chlordane concentrations were measured in air sampled from a tower on the south shore of Bermuda and in Sargasso Sea surface water approximately 80 to 320 kilometers south of Bermuda. The atmospheric chlorinated hydrocarbons appeared to be gaseous, and the DDT concentration was two orders of magnitude higher than previously reported particulate values. The PCB and DDT were enriched in the surface microlayer (150 micrometers) relative to their concentrations in water at a depth of 30 centimeters. Atmospheric residence times for PCB and DDT of 40 to 50 days, calculated from the concentrations in the air and water, are 20 times shorter than values previously estimated for DDT from rainfall and DDT production data.  相似文献   

15.
Unusual concentrations of dissolved two- to four-carbon alkanes were observed in the waters in Norton Sound in a localized area approximately 40 kilometers south of Nome, Alaska, in 1976. The hydrocarbons were identified in the near-bottom waters downcurrent for more than 100 kilometers from a sea-floor point source. Preliminary dynamic modeling estimates of the initial gas phase composition predict methanelethane and ethanelpropane ratios of 24 and 1.7, respectively, assuming the hydrocarbons were introduced by bubbles. The low ethanelpropane ratio is indicative of gas from a liquid petroleum source rather than from nonassociated or biogenic natural gas. Preliminary data on the structural geology of Norton Basin lend support to the interpretation based on the hydrocarbon plume. Unconformably truncated strata dip basinward from the seep locus; acoustic anomalies and numerous steeply dipping faults in the immediate vicinity of the seep are corroborating evidence that shallow gas- or petroleum-charged sediments and strata coincide with avenues for migration of mobile hydrocarbons to the sea floor. These factors, taken in concert with the sedimentological regime, the recent revision (increase) of basin depth estimates, and the highly localized hydrocarbon source, strongly suggest a thermogenic rather than a recent biogenic origin for these gaseous compounds.  相似文献   

16.
Infrared observations of Io during the 1986 apparition of Jupiter indicate that a large eruptive event occurred on the leading side of Io on 7 August 1986, Universal Time. Measurements made at 4.8, 8.7, and 20 micrometers suggest that the source of the event was about 15 kilometers in radius with a model temperature of approximately 900 Kelvin. Together with previously reported events, these measurements indicate that high-temperature volcanic activity on the leading side of Io may be more frequent than previously thought. The inferred temperature is significantly above the boiling point of sulfur in a vacuum(715 Kelvin) and thus constitutes strong evidence for active silicate volcanism on the surface of Io.  相似文献   

17.
Mantle plume helium in submarine basalts from the galapagos platform   总被引：1，自引：0，他引：1  
Helium-3/helium-4 ratios in submarine basalt glasses from the Galapagos Archipelago range up to 23 times the atmospheric ratio in the west and southwest. These results indicate the presence of a relatively undegassed mantle plume at the Galápagos hot spot and place Galápagos alongside Hawaii, Iceland, and Samoa as the only localities known to have such high helium-3/helium-4 ratios. Lower ratios across the rest of the Galápagos Archipelago reflect systematic variations in the degree of dilution of the plume by entrainment of depleted material from the asthenosphere. These spatial variations reveal the dynamics of the underlying mantle plume and its interaction with the nearby Galápagos Spreading Center.  相似文献   

18.
On the basis of presently available data, combined with present-day knowledge of the physics and chemistry of cloud particle development, it is possible to make the following generalizations about the mode of precipitation in natural clouds. 1) The all-water mechanism begins to operate as soon as a parcel of cloud air is formed and continues to operate throughout the life of the cloud. The ice-crystal mechanism, on the other hand, can begin to operate only after the top of the cloud has reached levels where ice nuclei can be effective (about -15 degrees C). Some clouds never reach this height; any precipitation from them must be through the all-water mechanism. In cold climates and at high levels in the atmosphere, the cloud bases may be very close to this critical temperature. In the tropics, approximately 25,000 feet separate the bases of low clouds from the natural ice level. 2) The number of large hygroscopic nuclei in maritime air over tropical oceans is entirely adequate to rain-out any cloud with a base below about 10,000 feet, provided the cloud duration and cloud depth is sufficient for the precipitation process to operate. Extensive trajectories over land will decrease the number of sea-salt particles, both because of sedimentation and removal in rain. Measurements show an order-of-magnitude decrease in the number of large particles as maritime air moves from the Gulf of Mexico to the vicinity of St. Louis, during the summer months. Measurements in Arizona and New Mexico show even smaller chloride concentrations, presumably because of the long overland trajectories required in reaching these areas. The maritime particles lost in overland trajectories apparently are more than replaced by particles of land origin. The latter are usually of mixed composition and are less favorable for the formation of outsized solution droplets. 3) Ice nuclei, required for the formation of ice crystals and for droplet freezing, are rather rare at temperatures higher than about -10 degrees C. This, of course, accounts for the fact that natural clouds undergo extensive undercooling. Because of the scarcity of suitable nuclei, precipitation through the ice phase usually is not found in clouds warmer than about -15 degrees to -20 degrees C. Natural cirrus clouds might provide ice nuclei for precipitation at somewhat higher temperatures, but this possibility has not been extensively studied. 4) Precipitation in tropical clouds invariably first develops through the all-water mechanism; points discussed in paragraphs 1, 2, and 3 above all work toward this end. Tropical clouds which reach to heights above about 25,000 feet also develop precipitation through snow pellets. The data for mid-latitude clouds are conflicting. Some measurements suggest that summer clouds in the central United States and in the semiarid Southwest develop rain largely through the all-water process; existing theories support such a suggestion. However, flight measurements indicate that there is considerably more ice and snow in the clouds than can be accounted for by present theory; as a consequence, one must be careful in ruling out the ice mechanism in these areas. It appears to me, however, that the ice particles in these clouds are best accounted for through the hypothesis of freezing of drops which have grown to fairly large size through diffusion of vapor. Thus, the ice would be only incidental to the precipitation development. Winter clouds in the central United States and almost all of the clouds of northern United States and Canada appear to precipitate largely through the ice-crystal mechanism. The relatively cold cloud bases and the continental sources of air masses in these regions appear to retard the warm-rain mechanism to the point where the ice mechanism dominates. But here again, a great deal of research must be completed before a firm conclusion can be drawn (18).  相似文献   

19.
银杏叶提取物对氧自由基的影响   总被引：3，自引：0，他引：3  
分别提取银杏叶脂溶性成分和水溶性成分,采用NBT(氯化硝基四氮唑蓝)光还原法检测银杏叶提取物消除氧自由基能力的大小,并计算出抑制率。结果表明:银杏叶脂溶性成分和水溶性成分均能消除氧自由基,水溶性成分消除氧自由基的能力强于脂溶性成分。水溶性提取物组的活力单位是0.167mg,脂溶性提取物NaOH组的活力单位是0.17mg,脂溶性提取物无水乙醇组的活力单位是0.795mg。  相似文献   

20.
Halite particles about 2 micrometers in size were collected by a quartz crystal microbalance cascade impactor from the El Chichón eruption cloud in the lower stratosphere during April and May 1982. These particles are probably derived from the erupted chloride-rich, alkalic magma. Enrichments of hydrogen chloride and increases in optical depolarization in the eruption cloud observed by lidar measurements may reflect the influence of the halite particles. There is evidence that the halite particles reacted with sulfuric acid after about 1 month, releasing gaseous hydrogen chloride, which can influence the catalytic destruction of ozone in the stratosphere.  相似文献   

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