10,008 research outputs found
Atmospheric transport and deposition of Indonesian volcanic emissions
International audienceA regional climate model has been used to study the transport and deposition of sulfur (SO2 and SO42-) and PbCl2 emissions from Indonesian volcanoes. The sensitivity of the atmospheric loss of these trace species to meteorological conditions and their solubility was examined. Two experiments were conducted: 1) volcanic sulfur released as primarily SO2 and subject to transport, deposition, and oxidation to SO42-; and 2) PbCl2 released as an infinitely soluble passive tracer subject to only transport and deposition. The first experiment was used to calculate SO2 loss rates from each active Indonesian volcano producing an annual mean loss rate for all volcanoes of 1.1Ă—10-5 s-1, or an e-folding rate of approximately 1 day. SO2 loss rate was found to vary seasonally, be poorly correlated with wind speed, and uncorrelated with temperature or relative humidity. The variability of SO2 loss rates is found to be correlated with the variability of wind speeds, suggesting that it is much more difficult to establish a "typical'' SO2 loss rate for volcanoes that are exposed to changeable winds. Within an average distance of 70 km away from the active Indonesian volcanoes, 53% of SO2 loss is due to conversion to SO42-, 42% due to dry deposition, and 5% due to lateral transport away from the dominant direction of plume travel. The solubility of volcanic emissions in water is shown to influence their atmospheric transport and deposition. High concentrations of PbCl2 are predicted to be deposited near to the volcanoes while volcanic S travels further away until removal from the atmosphere primarily via the wet deposition of H2SO4. The ratio of the concentration of PbCl2 to SO2 is found to exponentially decay at increasing distance from the volcanoes. The more rapid removal of highly soluble species should be considered when observing SO2 in an aged plume and relating this concentration to other volcanic species. An assumption that the ratio between the concentrations of highly soluble volcanic compounds and SO2 within a plume is equal to that observed in fumarolic gases is reasonable at small distances from the volcanic vent, but will result in an underestimation of the emission flux of highly soluble species
ESD Ideas: A 6-year oscillation in the whole Earth system?
An oscillation of about 6 years has been reported in Earth’s fluid core motions, magnetic field, rotation, and crustal deformations. Recently, a 6-year cycle has also been detected in several climatic parameters (e.g., sea level, surface temperature, precipitation, land ice, land hydrology, and atmospheric angular momentum). Here we suggest that the 6-year oscillations detected in the Earth’s deep interior, mantle rotation, and atmosphere are linked together, and that the core processes previously proposed as drivers of the 6-year cycle in the Earth’s rotation, cause in addition the atmosphere to oscillate together with the mantle, inducing fluctuations in the climate system with similar periodicities.</p
An algorithm for correction of atmospheric scattering dilution effects in volcanic gas emission measurements using skylight differential optical absorption spectroscopy
Differential Optical Absorption Spectroscopy (DOAS) is commonly used to measure gas emissions from volcanoes. DOAS instruments measure the absorption of solar ultraviolet (UV) radiation scattered in the atmosphere by sulfur dioxide (SO2) and other trace gases contained in volcanic plumes. The standard spectral retrieval methods assume that all measured light comes from behind the plume and has passed through the plume along a straight line. However, a fraction of the light that reaches the instrument may have been scattered beneath the plume and thus has passed around it. Since this component does not contain the absorption signatures of gases in the plume, it effectively “dilutes” the measurements and causes underestimation of the gas abundance in the plume. This dilution effect is small for clean-air conditions and short distances between instrument and plume. However, plume measurements made at long distance and/or in conditions with significant atmospheric aerosol, haze, or clouds may be severely affected. Thus, light dilution is regarded as a major error source in DOAS measurements of volcanic degassing. Several attempts have been made to model the phenomena and the physical mechanisms are today relatively well understood. However, these models require knowledge of the local atmospheric aerosol composition and distribution, parameters that are almost always unknown. Thus, a practical algorithm to quantitatively correct for the dilution effect is still lacking. Here, we propose such an algorithm focused specifically on SO2 measurements. The method relies on the fact that light absorption becomes non-linear for high SO2 loads, and that strong and weak SO2 absorption bands are unequally affected by the diluting signal. These differences can be used to identify when dilution is occurring. Moreover, if we assume that the spectral radiance of the diluting light is identical to the spectrum of light measured away from the plume, a measured clean air spectrum can be used to represent the dilution component. A correction can then be implemented by iteratively subtracting fractions of this clean air spectrum from the measured spectrum until the respective absorption signals on strong and weak SO2 absorption bands are consistent with a single overhead SO2 abundance. In this manner, we can quantify the magnitude of light dilution in each individual measurement spectrum as well as obtaining a dilution-corrected value for the SO2 column density along the line of sight of the instrument. This paper first presents the theory behind the method, then discusses validation experiments using a radiative transfer model, as well as applications to field data obtained under different measurement conditions at three different locations; Fagradalsfjall located on the Reykjanaes peninsula in south Island, Manam located off the northeast coast of mainland Papua New Guinea and Holuhraun located in the inland of north east Island
Public Space Users' Soundscape Evaluations in Relation to Their Activities. An Amsterdam-Based Study
Combination of Vorinostat with Whole-brain Radiotherapy in the Treatment of Brain Metastases
Background: A third of patients with solid malignancies develop brain metastases. Expected overall survival is 4-7 months depending on age, performance status, and extracranial disease. Standard treatment is controversial; however, the majority of patients receive wholebrain radiation therapy at some point. Vorinostat (suberoylanilide hydroxamic acid, SAHA), an FDA-approved HDAC inhibitor, has been demonstrated to radiosensitize tumor cells in vitro, as assessed by both radiation-induced DNA damage and clonogenic cell survival (Munshi et al. Molecular Cancer Therapeutics 5, 1967-1974, 2006). We have shown that vorinostat downregulates key genes involved in double-strand DNA repair (Rad50, Rad51, XRCC2, XRCC3, XRCC6), as assessed by quantitative PCR. This suggests that the drug’s mechanism of radiosensitization is epigenetic coordinated inhibition of the DNA repair process. We hypothesize that the combination of vorinostat with whole-brain radiation therapy will be both safe and efficacious.
American Society of Clinical Oncology (ASCO) 46th Annual Meeting June 4-8, Chicago, IL
Anisotropic splitting of intersubband spin plasmons in quantum wells with bulk and structural inversion asymmetry
In semiconductor heterostructures, bulk and structural inversion asymmetry
and spin-orbit coupling induce a k-dependent spin splitting of valence and
conduction subbands, which can be viewed as being caused by momentum-dependent
crystal magnetic fields. This paper studies the influence of these effective
magnetic fields on the intersubband spin dynamics in an asymmetric n-type
GaAs/AlGaAs quantum well. We calculate the dispersions of intersubband spin
plasmons using linear response theory. The so-called D'yakonov-Perel'
decoherence mechanism is inactive for collective intersubband excitations,
i.e., crystal magnetic fields do not lead to decoherence of spin plasmons.
Instead, we predict that the main signature of bulk and structural inversion
asymmetry in intersubband spin dynamics is a three-fold, anisotropic splitting
of the spin plasmon dispersion. The importance of many-body effects is pointed
out, and conditions for experimental observation with inelastic light
scattering are discussed.Comment: 8 pages, 6 figure
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