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At least 433 records · Page 24

Evaporation kinetics in the hanging drop method of protein crystal growth

An engineering analysis of the rate of evaporation of solvent in the hanging drop method of protein crystal growth is presented; these results are applied to 18 different drop and well arrangements commonly encountered in the laboratory, taking into account the chemical nature of the salt, the drop size and shape, the drop concentration, the well size, the well concentration, and the temperature. It is found that the rate of evaporation increases with temperature, drop size, and with the salt concentration difference between the drop and the well. The evaporation possesses no unique half-life. Once the salt in the drop achieves about 80 percent of its final concentration, further evaporation suffers from the law of diminishing returns.

Baird, James K.↗

Cosmic-ray lifetime in the Galaxy - Experimental results and models

The separation of the cosmic-ray Be isotopes achieved by two satellite experiments is discussed. From the measured isotopic ratio between the radioactive Be-10 (half-life = 1,500,000 years) and the stable Be-9, it is deduced that the cosmic rays propagate through matter with an average density of 0.24 = or - 0.07 atoms/ cu cm. The implications of this result for the cosmic-ray age is reviewed in the context of two models of confinement and propagation: the homogeneous model, normally identified with confinement ot the galactic gaseous disk, and a diffusion model in which the cosmic rays extend into a galactic halo. A newly deduced cosmic-ray pathlength distribution, a self-consistent model of solar modulation, and a set of fragmentation cross sections are calculated. It is concluded that in a homogeneous model, the cosmic-ray age is 15 (+7, -4) million years, about a factor longer than early estimates based on the abundances of the light nuclei Li, Be, and B and a nominal interstellar density of 1 atom/ cu cm.

Simpson, J. A.↗

Examination of Martian sedimentary rocks to understand possible paleo-ocean and its age

It is well known that the terrestrial marine sediments have large cerium anomaly on their chondrite-normalized REE pattern. Siliceous shale and calcaleous sediments have negative Ce-anomaly. Ferromanganese nodule have positive or negative Ce-anomaly. The Ce-anomaly is considered to be a result of tetravalent state of cerium rather than common trivalent. Ferromanganese nodule which formed under reducing condition has negative Ce-anomaly. Then, combined study of Ce-anomaly with Ce isotopes is expected to play an important role in geochemistry. La-138 decays to Ce-138 and Ba-138 with a total half life of about 1 x 10 to the 11th years. Cerium anomalies (positive or negative) are expected in Martian paleo-ocean and in sediments as observed in the terrestrial environment. A list of things to be examined is given.

Tanaka, T.↗

Circumstellar material in meteorites - Noble gases, carbon and nitrogen

In addition to preserving a record of isotopically distinct reservoirs in the early solar system, some primitive meteorites contain discrete grains of presolar origin. Such grains are distinguished by the isotopically anomalous noble-gas components they contain. One such component consists of monoisotopic Ne-22, produced by decay of radioactive Na-22 with a 2.6 yr half-life. Two xenon components have also been identified: one synthesized apparently in a supernova, the other probably in a red giant star. Most of the grains that carry these noble-gas components are carbonaceous and contain isotopically anomalous C, N, or both. They include diamond and silicon carbide. Two unidentified carriers of isotopically anomalous nitrogen, unaccompanied by noble gases, occur in the brecciated stony iron meteorite, Bencubbin.

Anders, Edward↗

Evidence from the Semarkona ordinary chondrite for Al-26 heating of small planets

The first observation of radiogenic Mg-26 in nonrefractory meteoritic material, a plagioclase-bearing, olivine-pyroxene clast chondrule in the Semarkona ordinary chondrite, is reported. The inferred initial abundance of Al-26 is sufficient to produce incipient melting in well-insulated bodies of chondritic composition. It is concluded that planetary accretion and diffentiation must have begun on a timescale comparable to the half-life of Al-26 and that, even if widespread melting did not occur, Al-26 heating played a significant role in thermal metamorphism on small planets.

Hutcheon, I. D.↗

Update on terrestrial ages of Antarctic meteorites

Cosmic-ray produced Cl-36 (half-life = 3.01 x 10 to the 5th years) has been measured in 90 Antarctic meteorites by accelerator mass spectrometry. The terrestrial ages of the meteorites were calculated from the results. After excluding possible paired objects, 138 terrestrial ages from 18 different locations are available from C-14, Kr-81, and Cl-36 measurements for application to Antarctic meteorite and glaciological studies. The terrestrial ages of Allan Hills meteorites vary from 2000 years to 1 million years and are clearly longer than those of Yamato meteorites and other Antarctic meteorites. The oldest Allan Hills meteorites were found close to the eastern edge and in the southeast of the main icefield. Among all Antarctic meteorites measured to date, only L and LL chondrites have terrestrial ages older than 370,000 years.

Nishiizumi, K.↗

Surface-catalyzed air oxidation of hydrazines: Environmental chamber studies

The surface-catalyzed air oxidation reactions of fuel hydrazines were studied in a 6500-liter fluorocarbon-film chamber at 80 to 100 ppm concentrations. First-order rate constants for the reactions catalyzed by aluminum, water-damaged aluminum (Al/Al2O3), stainless steel 304L, galvanized steel and titanium plates with surface areas of 2 to 24 sq m were determined. With 23.8 sq m of Al/Al2O3 the surface-catalyzed air oxidation of hydrazine had a half-life of 2 hours, diimide (N2H2) was observed as an intermediate and traces of ammonia were present in the final product mixture. The Al/Al2O3 catalyzed oxidation of monomethylhydrazine yielded methyldiazine (HN = NCH3) as an intermediate and traces of methanol. Unsymmetrical dimethylhydrazine gave no detectable products. The relative reactivities of hydrazine, MMH and UDMH were 130 : 7.3 : 1.0, respectively. The rate constants for Al/Al2O3-catalyzed oxidation of hydrazine and MMH were proportional to the square of the surface area of the plates. Mechanisms for the surface-catalyzed oxidation of hydrazine and diimide and the formation of ammonia are proposed.

Kilduff, Jan E.↗

The 10.7-cm microwave observations of AR 5395 and related terrestrial effects

The 10.7 cm flux patrols in Canada recorded 4 Great Bursts (peaks greater than 500 sfu) during the disk passage of AR 5395 in March 1989. The Great Bursts of 16 and 17 March were simple events of great amplitude and with half-life durations of only several minutes. Earlier Great Bursts, originating on 6 March towards the NE limb and on 10 March closer to the central meridian, belong to an entirely different category of event. Each started with a very strong impulsive event lasting just minutes. After an initial recovery, however, the emission climbed back to level as greater or greater than the initial impulsive burst. The events of 6 and 10 March stayed above the Great Burst threshold for at least 100 minutes. The second component of long duration in these cases is associated with Type 4 continuum emission and thus very likely with CMEs. Major geomagnetic disturbances did not occur as a result of the massive complex event of 6 March or the two simple but strong events of 16 and 17 March. But some 55 hours after the peak in the long-enduring burst of 10 March, a storm began which qualifies as the fourth strongest geomagnetic storm in Canada since 1932. The vertical component of the earth's field measured during the storm by a fluxgate magnetometer at a station in Manitoba is presented. Within a minute of the sudden commencement of this storm, a series of breakdowns began in the transmission system of Hydro-Quebec which resulted in a total loss of power, on a bitterly cold winter's day, for at least 10 hours. The loss of power provoked an enormous outcry from the public resulting in the power utilities being more receptive to the need to monitor solar as well as geomagnetic activity.

Gaizauskas, V.↗

Ozone profile measurements of McMurdo Station, Antarctica, during the spring of 1987

Ozone and temperature profiles were measured in 50 balloon flights at McMurdo Station (78 deg S) during the spring of 1987. Compared to similar data obtained in 1986, stratospheric temperatures were lower and the spring time Antarctic ozone reduction was greater in magnitude, extended to higher altitude, and proceeded at a higher rate in 1987. Ozone partial pressures reached values as low as 3 nbar (as compared to about 10 nbar in 1986) in the 16- to 18-km region in early and late October, down from about 150 nbar in late August. These low values suggest essentially complete removal of ozone in this region. The upper boundary of the depletion region was observed to be 2-3 km higher than in 1986, extending to altitudes as high as 24 km in mid-September. When averaged over September, the ozone mixing ratio at 18 km decayed with a half-life of only 12.4 days, as compared to about 28 days in 1986. Adiabatic vertical motions over 1- to 2-km intervals between 12 and 20 km with consequent ozone reductions were observed in association with the formation of nacreous clouds, indicating these to be rare events on a local scale probably associated with mountain lee waves.

Hofmann, D. J.↗

A search for the 478 keV line from the decay of nucleosynthetic Be-7

Unstable Be-7 (half-life 53.28 days) is expected to be present in the ejecta of classical novae. If the frequency of novae in the central Galaxy is high enough, a nearly steady state abundance of Be-7 will be present there. Data accumulated during transits of the Galactic center across the aperture of the Solar Maximum Mission Gamma Ray Spectrometer have been searched for evidence of the 478 keV gamma-ray line resulting from Be-7 decay. A 3-sigma upper limit of 0.00016 gamma/sq cm s has been placed on the emission in this line from the central radian of the Galactic plane. Less stringent limits have been set on the production of Be-7 in Nova Aquilae 1982, Nova Vulpeculae 1984 No. 2, and Nova Centauri 1986 from observations with the same instrument.

Harris, Michael J.↗

The interactions of atmospheric cosmogenic radionuclides with spacecraft surfaces

The discovery of the cosmogenic radionuclide Be-7 on the front surface (and the front surface only) of the Long Duration Exposure Facility (LDEF) spacecraft has opened opportunities to investigate new phenomena in several disciplines of space science. The experiments performed for this work show that the Be-7 results only if the source of the isotope is the atmosphere through which the spacecraft passed. We should expect that the uptake of beryllium in such circumstances will depend on the chemical form of the Be and the chemical nature of the substrate. It was found that the observed concentration of Be-7 does, in fact, differ between metal surfaces and organic surfaces such as PTFE (teflon). It is noted, however, that: (1) organic surfaces, even PTFE, are etched by the atomic oxygen found under these orbital conditions, and (2) the relative velocity of the species is 8 km(exp -1)s relative to the surface and the interaction chemistry and physics may differ from the norm. The Be-7 is formed by spallation of O and N nuclei under cosmic ray proton bombardment. The principal source region is at altitudes of 12-15 km. While very small quantities are produced above 300 km, the amount measured on the LDEF was 3 to 4 orders of magnitude higher than expected from production at orbital attitude. The most reasonable explanation is that Be-7 is rapidly transported from low altitudes by some unknown mechanism. The process must take place on a time scale similar to the half-life of the isotope (53 days). Many other isotopes are produced by cosmic ray reactions, and some of these are suited to measurement by the extremely sensitive methods of accelerator mass spectrometry. A program was initiated to search for these isotopes and it is hoped that such studies will provide new methods for studying mixing in the upper atmosphere.

Gregory, John C.↗

Terrestrial production vs. extraterrestrial delivery of prebiotic organics to the early Earth

A comprehensive treatment of comet/asteroid interaction with the atmosphere, ensuring surface impact, and resulting organic pyrolysis is required to determine whether more than a negligible fraction of the organics in incident comets and asteroids actually survived collision with Earth. Results of such an investigation, using a smoothed particle hydrodynamic simulation of cometary and asteroidal impacts into both oceans and rock, demonstrate that organics will not survive impacts at velocities approx. greater than 10 km s(exp -1), and that even comets and asteroids as small as 100m in radius cannot be aerobraked to below this velocity in 1 bar atmospheres. However, for plausible dense (10 bar CO2) early atmospheres, there will be sufficient aerobraking during atmospheric passage for some organics to survive the ensuing impact. Combining these results with analytical fits to the lunar impact record shows that 4.5 Gyr ago Earth was accreting at least approx. 10(exp 6) kg yr(exp 1) of intact cometary organics, a flux which thereafter declined with a approx. 100 Myr half-life. The extent to which this influx was augmented by asteroid impacts, as well as the effect of more careful modelling of a variety of conservative approximations, is currently being quantified. These results may be placed in context by comparison with in situ organic production from a variety of terrestrial energy sources, as well as organic delivery by interplanetary dust. Which source dominated the early terrestrial prebiotic inventory is found to depend on the nature of the early terrestrial atmosphere. However, there is an intriguing symmetry: it is exactly those dense CO2 atmospheres where in situ atmospheric production of organic molecules should be the most difficult, in which intact cometary organics would be delivered in large amounts.

Chyba, C. F.↗

The interactions of atmospheric cosmogenic radionuclides with spacecraft surfaces

The discovery of the cosmogenic radionuclide Be-7 on the front surface of the Long Duration Exposure Facility (LDEF) spacecraft has opened opportunities to investigate new phenomena in several disciplines of space science. The experiments performed for this work show that the Be-7 results only if the source of the isotope is the atmosphere through which the spacecraft passed. We should expect that the uptake of beryllium in such circumstances will depend on the chemical form of the Be and the chemical nature of the substrate. It was found that the observed concentration of Be-7 does, in fact, differ between metal surfaces and organic surfaces such as PTFE (teflon). It is noted, however, that: (1) organic surfaces, even PTFE, are etched by the atomic oxygen found under these orbital conditions, and (2) the relative velocity of the species is 8 km(exp -1)s relative to the surface and the interaction chemistry and physics may differ from the norm. The Be-7 is formed by spallation of O and N nuclei under cosmic ray proton bombardment. The principal source region is at altitudes of 12-15 km. While very small quantities are produced above 300 km, the amount measured on the LDEF was 3 to 4 orders of magnitude higher than expected from production at orbital altitude. The most reasonable explanation is that Be-7 is rapidly transported from low altitudes by some unknown mechanism. The process must take place on a time scale similar to the half-life of the isotope (53 days). Many other isotopes are produced by cosmic ray reactions, and some of these are suited to measurement by the extremely sensitive methods of accelerator mass spectrometry. A program was initiated to search for these isotopes and it is hoped that such studies will provide new methods for studying mixing in the upper atmosphere.

Gregory, J. C.↗

Criticality of Be-7 concentration in LDEF

Heretofore, a number of papers reported the detection of high Be-7 concentration in the LDEF. It sounded alarming for space flight in the LDEF orbit, since Be-7 has a half life of 54 days and emits gamma rays of 0.48 MeV which is ionizing radiation. Two concerns are raised: the high concentration of harmful rays to spacecraft crews; and the concentration damage to spacecraft electronic components. A need was established to estimate the dosage of this concentration and compare the value of the allowed limits. As a result, the dosage was calculated of 0.03 rad. When this is compared with the human limit of 25 rads and the susceptibility requirement of 800 rads, the Be-7 amount should not be considered critical. The calculation of Be-7 dosage is detailed.

Young, Poh Shien↗

Cosmogenic radioisotopes on LDEF surfaces

The radioisotope Be-7 was discovered in early 1990 on the front surface, and the front surface only, of the LDEF. A working hypothesis is that the isotope, which is known to be mainly produced in the stratosphere by spallation of nitrogen and oxygen nuclei with cosmic ray protons or secondary neutrons, diffuses upward and is absorbed onto metal surfaces of spacecraft. The upward transport must be rapid, that is, its characteristic time scale is similar to, or shorter than, the 53 day half-life of the isotope. It is probably by analogy with meteoritic metal atmospheric chemistry, that the form of the Be at a few 100 km altitude is as the positive ion Be(+) which is efficiently incorporated into the ionic lattice of oxides, such as Al2O3, Cr2O3, Fe2O3, etc., naturally occurring on surfaces of Al and stainless steel. Other radioisotopes of Be, Cl, and C are also produced in the atmosphere, and a search was begun to discover these. Of interest are Be-10 and C-14 for which the production cross sections are well known. The method of analysis is accelerator mass spectrometry. Samples from LDEF clamp plates are being chemically extracted, purified, and prepared for an accelerator run.

Gregory, J. C.↗

How Mars lost its atmosphere

There is a widespread suspicion that Mars thin atmosphere is in some way attributable to the planet's size. Another possibility is that the atmosphere was never degassed or outgassed in the first place. I prefer escape. Hydrodynamic escape (vigorous thermal escape) and impact erosion (expulsion of atmosphere by impacts) are two processes that should have been operative early. Although in principle hydrodynamic escape could have shrunk Mars atmosphere a hundredfold while leaving the composition of the remnant atmosphere nearly unaltered, very high escape fluxes are required. The implicated escape mechanism must have been efficient, nearly non-fractionating, and vastly more potent for Mars than for Earth or Venus. Impact erosion is an appealing candidate. Noble gases are the obvious first test. Noble gases are the most volatile elements and so are the most likely to have been affected by impact erosion and the easiest to address quantitatively. Xenon in particular imposes three constraints on how Mars lost its atmosphere: (1) the very low abundance of nonradiogenic Xe abundance of nonradiogenic Xe compared to Earth, Venus, and likely meteoritic sources; (2) its nonradiogenic isotopes distinct from likely meteoritic sources; and (3) the relatively high absolute abundance of radiogenic daughter of the extinct radionuclide I-129 (half-life 17 Myr). In impact erosion, the first two become constraints on the composition, mass distribution, and orbital elements of the impactors. The third requires that Mars lost its nonradiogenic Xe early, probably before it was 100 Myr old. Impact erosion can explain Mars by any of three stories. (1) Mars in unlikely. In a sort of planetary brinkmanship, impact erosion almost removed the entire atmosphere but was arrested just in time. (2) Martian noble gases are cometary and cometary Xe is as isotopically mass fractionated as Martian and terrestrial Xe. This is most easily accomplished if a relatively thick geochemically controlled CO2 atmosphere protected trace atmophiles against escape. (3) Mars was indeed stripped of its early atmosphere but a small remnant was safely stored in the regolith, later released as a byproduct of water mobilization.

Zahnle, Kevin↗

Forsterite/melt partitioning of argon and iodine: Implications for atmosphere formation by outgassing of an early Martian magma ocean

Argon and Xe in the Martian atmosphere are radiogenic relative to the Martian mantle if the SNC meteorites are from Mars. Decay of the short lived isotope I-129 to Xe-129 (t sub 1/2 = 16 m.y.) is the most plausible source of the radiogenic Xe. This short half life constrains any process responsible for the elevated Xe-129/Xe-132 ratio of the Martian atmosphere to occur very early in solar system history. Musselwhite et al. proposed that the differential solubility of I and Xe in liquid water played a key role in producing the radiogenic signature in the Martian atmosphere. Here we explore an alternative hypothesis involving purely igneous processes, and motivated in part by new experimental results on the partitioning of I and Xe between minerals and melt.

Musselwhite, Donald S.↗

Rhenium-osmium isotope systematics in meteorites. I - Magmatic iron meteorite groups IIAB and IIIAB

Resonance ionization mass spectrometry is used to determine the Re and Os abundances by isotope dilution (ID) and to measure Os-187/Os-186 ratios from 19 iron meteorites. Abundances range from 1.4 to 4800 ppb Re, and from 13 to 65,000 ppb Os, and generally agree well with previous ID and neutron activation results. The Re and Os data suggest that abundance trends in these iron groups may be entirely explained by fractional crystallization. Whole-rock isochrons for the IIAB and IIIAB groups are statistically indistinguishable. Pooled data yield an initial Os-187/Os-186 of 0.794 +/- 0.010 Ga. Given the errors in the slope and half life, this age does not differ significantly from the canonical chondrite age of 4.56 Ga, but could be as young as 4.46 Ga.

Morgan, John W.↗