The lunar atmosphere Scientific report
Lunar atmosphere data and postulated theory of its structure
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Lunar atmosphere data and postulated theory of its structure
Solar wind sputtering of the lunar surface helps determine the composition of the lunar exosphere and contributes to surface weathering. To date, only the effects of the two dominant solar wind constituents, H+ and He+, have been considered. The heavier, less abundant solar wind constituents have much larger sputtering yields because they have greater mass (kinetic sputtering) and they are highly charged (potential sputtering) Their contribution to total sputtering can therefore be orders of magnitude larger than their relative abundances would suggest
NASA’s Artemis program has the lofty goal of creating a sustained lunar presence to provide unprecedented opportunities for scientific discovery and to ensure American industry’s access to the unlimited resources and commercial potential in space. To achieve this goal, NASA must incrementally develop and expand its capabilities beyond the short lunar stays of the Apollo program to a robust continued presence with infrastructure and equipment to reduce mission risk by providing safer and more reliable access to the surface, its resources, and protection from the environment. Kennedy Space Center’s Swamp Works Granular Mechanics and Regolith Operations laboratory has partnered with AI SpaceFactory to develop the architectural and structural design of a robotically constructable unpressurized shelter. The shelter, called Lina is designed to protect astronauts and surface assets from radiation, meteoroid impact, moon quakes and thermal gradients. A Fused Filament Fabrication (FFF) construction process using regolith polymer composites was developed. The construction system and associated print parameters are discussed along with the environmental simulation equipment and a summary of test conditions. Test samples were printed in simulated lunar dirty thermal vacuum conditions (~-180 C, ~10-3 torr) and subjected to a series of tests. The resulting strength properties are summarized here, the full details of the material characteristics are provided in a related paper. Lina’s structural design criteria and the resulting initial structure design are detailed in two related papers, this paper presents an update to Lina’s design based on the achieved material strength properties. Finally, a scaled down version of the updated Lina was built on a regolith simulant surface using a novel anchoring technique in simulated lunar vacuum conditions.
In response to the Discovery announcement of opportunity a team consisting of TRW Lewis Research Center, JPL and UCLA with scientific co-investigators from government and University laboratories have proposed to fly the first planetary solar electric propulsion (SEP) mission. Diana is designed to carry an X-ray and gamma ray spectrometer, and imaging spectrometer, a framing camera, a laser altimer an ion spectrometer and a magnetometer. In order to obtain lunar gravity data from the far side of the moon a relay satellite is placed into high polar orbit about the moon to relay the Doppler-shifted telemetry to Earth. Diana will spend two months in a 700 km polar orbit obtaining mineralogical data from a full spectral map of the lunar surface, and then spend a year in a 100 km (or below) polar orbit mapping the lunar elemental composition, its topography, gravity field, ions from its atmosphere and its permanent and induced magnetic fields. After the low altitude mapping phase the ion thrusters propel the spacecraft out of the lunar sphere of influence and onto a heloioscentric trajectory to rendezvous with dormant comet Wilson-Harrington. The ground truth provided by the returned lunar samples to validate the remote sensing instruments for lunar studies will also serve to validate the Wilson-Harrington observations since the same instruments will be used at both bodies.
The suggestion of O'Keefe (1980) that the terminal Eocene event was caused by rings of tektite material encircling the earth is discussed. It is argued that the assumption that the tektites are of lunar volcanic origin is unwarranted and contrary to existing data, including the lack of lunar rocks of suitable composition, the lack of lunar rocks of the correct age, the lack of evidence that the North American tektites fell throughout a sedimentary rock column of a few million years, and the nondetection of a tektite with a measurable cosmic ray exposure age. Alternatively, it is suggested that the terminal Eocene event may be associated with volcanic ash, air-fall tuff and bentonite in the late Eocene. O'Keefe replies that the hypothesis of the terrestrial origin of the tektites conflicts with the laws of physics, for example in the glass structure and shaping of the tektites. Furthermore, evidence is cited for lunar rocks of the proper major-element composition and ages, and it is noted that the proposed solar Poynting-Robertson effect would account for the particle fall distributions and cosmic ray ages.
Lunar meteorites are complementary to the suite of rock and regolith samples collected by the Apollo missions. While the Apollo samples represent the most pristine material we have from the Moon, lunar meteorites represent a more global sampling of the lunar crust, albeit without geologic context [e.g. 1]. As such, lunar meteorites are important for understanding the composition of the lunar crust and the processes responsible for its formation and evolution. This work aims to understand the observed differences in accessory phase chronology and volatile chemistry between lunar meteorites and Apollo rocks. For example, apatite ages in Apollo samples range from ~3.83 to 4.28 Ga [e.g. 2, 3], while apatites in lunar meteorites range from ~3.00 to 4.44 Ga [e.g. 4, 5]. Additionally, a much larger range of Cl isotope compositions and concentrations is observed in lunar meteorites as compared to Apollo samples[e.g. 6]. It has recently been shown that impact metamorphism can influence both chronology and chemistry of phosphates [e.g. 7, 8]. Here we present the first chronologic results from a consortium study pairing chronology, volatile chemistry, and crystal structure of apatites in a lunar breccia meteorite. The results of this work will help inform interpretation of ongoing analyses of apatites separated from Apollo soils. Note: Extended abstract on document.
Luna IX photographs indicate lunar surface composition of weakly cohesive poorly sorted fragmental material of unknown source
The Moon is significantly depleted in volatile elements when compared to Earth, an observation that has resulted in various formation scenarios leading to the loss of volatiles. Sodium is a moderately volatile element that is a lithophile, which can be utilized as a tracer of the volatile history in planetary bodies. It is also well observed in the exosphere of several bodies in our solar system and exoplanetary systems. But lunar surface sodium abundances have so far been measured only in samples brought back to Earth. We report on results from the first effort to provide a global-scale measurement of sodium on the lunar surface using X-ray fluorescent spectra from Chandrayaan-2. A global average of 1.33 ± 0.03 wt% derived here is higher than previously known. Trends in the sodium abundance indicate a long-lived adsorbate component that could explain the higher abundances reported here, which would act as a reservoir that sustains the lunar sodium exosphere.
Lunar chemical composition, hydrostatic equilibrium, thermal history and material evaporation are considered in a study of the internal structure of the moon
Determination of the elemental composition of lunar, asteroid, and planetary surfaces is a major concern for science and resource utilization of space. The science associated with the development of a satellite or lunar rover laser-mass spectrometer instrument is presented here. The instrument would include a pulsed laser with sufficient energy to create a plasma on a remote surface. Ions ejected from this plasma travel back to the spacecraft or rover, where they are analyzed by a time-of-flight mass spectrometer, giving the elemental and isotope composition. This concept is based on the LIMA-D instrument on board the former Soviet Union Phobos-88 spacecraft sent to Mars. A laser-mass spectrometer placed on a rover or satellite would substantially improve the data return over alternative techniques. The spatial resolution would be centimeters, and a complete mass spectrum could be achieved in one laser shot. An experiment is described that demonstrates these features. A 400 mj Nd:YAG laser is focused, to an intensity of 10(exp 11) w/sq cm, onto a Al, Ag, Cu, Ge, or lunar simulant target. A plasma forms from which ions are ejected. Some of these ions travel down an 18-m evacuated flight tube to a microchannel plate detector. Alternatively, the ions are captured by an ion trap where they are stored until pulsed into a 1-m time-of-flight mass spectrometer, giving the elemental composition of the remote surface. A television camera monitors the plasma plume shape, and a photodiode monitors the temporal plasma emission . With this system, ions of Al, Ag, Cu, Ge, and lunar simulant have been detected at 18 m. The mass spectrum from the ion trap and 1-m time-of-flight tube will be presented.
Lunar soil composition and environmental conditions in simulated study from available data, noting vacuum effect on silica and olivine
Two instruments, the gamma-ray spectrometer and the X-ray fluorescence spectrometer, are uniquely suited to the chemical mapping of planetary surfaces from orbit. Through their detection of characteristic line spectra they measure the concentrations of a suite of elements in each area overflown. Multielement chemical maps derived from these remote measurements are used in the construction of evolutionary models of planetary bodies and of the solar system as a whole. The NaI(T1) gamma-ray spectrometer and a gas proportional X-ray spectrometer were flown over 20 percent of the lunar surface during the Apollo 15 and 16 missions. These instruments measured chemical differences across the boundaries of known lunar provinces and revealed several new features of lunar-surface composition. Advanced spectrometers which are under development for future missions are able to educe much more information in a given time span than the Apollo instruments. They may be used in possible future missions such as Lunar Polar Orbiter, a Mars orbiter, a Mercury orbiter, outer planet satellite missions, rendezvous with asteroids and cometary nuclei, and surface-penetrating planetary probes.
The method of inferring photon spectra from an analysis of the measured pulse-height spectrum is considered along with the spectrum shape and its variation energy. The case is examined where photoelastic absorption predominates, and Compton scattering and pair production are negligible. The analytic method for obtaining the elemental composition from the observed lunar surface spectrum is described, and theoretical and calculated weight fraction fluxes for average lunar composition are tabulated.
Extra-mare basalts occupy 8.5% of the lunar basalt area and comprise 1% of the total mare basalt volume. They are preferentially located where the crust is thin and topographically low. In terms of age, eruption style, and composition they are as variable as the mare basalts. In some instances extrusion in extra-mare craters was preceded by floor-fracturing whereas in other cases it apparently was not. The volume of lava erupted may have been controlled more by the volume of magma produced than by hydrostatic effects. A minimum of nearly 1300 separate basalt eruptions is indicated; the true value could be nearer 30,000 separate eruptions.
Lunar soil composition determined to be porous fine-grain moderately cohesive rock powder, from Surveyor I and Luna IX pictures
Anorthosites occur ubiquitously within the lunar crust at depths of approx.3-30 km in apparent confirmation of the Lunar Magma Ocean (LMO) hypothesis. [1]. We will present recent chronological studies of anorthosites [2] that are relevant both to the LMO hypothesis and also to the lunar cataclysm hypothesis. Old (approx.4.4 Ga) Sm-Nd ages have been determined for some Apollo 16 anorthosites, and primitive initial Sr-87/Sr-86 ratios have been measured for several, but well-defined Rb-Sr ages concordant with the Sm-Nd ages have not been determined until now. Lunar anorthosite 67075, a Feldspathic Fragmental Breccia (FFB) collected near the rim of North Ray Crater, has concordant Sm-Nd and Rb-Sr ages of 4.47+/-0.07 Ga and 4.49+/-0.07 Ga, respectively. Initial Nd-143/Nd-144 determined from the Sm-Nd isochron corresponds to E(sub Nd,CHUR) = 0.3+/-0.5 compared to a Chondritic Uniform Reservoir, or E(sub Nd,HEDPB) = -0.6+/-0.5 compared to the initial Nd-143/Nd-144 of the HED Parent Body [3]. Lunar anorthosites tend to have E(sub Nd) > 0 when compared to CHUR, apparently inconsistent with derivation from a single lunar magma ocean. Although E(sub Nd) < 0 for some anorthosites, if lunar initial Nd-143/Nd-144 is taken equal to HEDR for the HED parent body [3], enough variability remains among the anorthosite data alone to suggest that lunar anorthosites do not derive from a single source, i.e., they are not all products of the LMO. An anorthositic clast from desert meteorite Dhofar 908 has an Ar-39-Ar-40 age of 4.42+/-0.04 Ga, the same as the 4.36-4.41+/-0.035 Ga Ar-39-Ar-40 age of anorthositic clast Y-86032,116 in Antarctic meteorite Yamato- 86032 [3,4]. Conclusions: (i) Lunar anorthosites come from diverse sources. Orbital geochemical studies confirm variability in lunar crustal composition [1, 5]. We suggest that the variability extends to anorthosites alone as shown by the Sm-Nd data (Fig. 2) and the existence of magnesian anorthosites (MAN, [6]) and "An93 anorthosites" [3,4]. (ii) Anorthositic clasts in lunar meteorites retain "high" Ar-Ar ages compared to Apollo anorthosites. This is perhaps a hint that "cataclysmic" impacts were on average less energetic in the mostly farside source regions of these meteorites than on the lunar nearside.
From comparing the mineral and chemical composition of regoliths with the compositions of primary magmatic lunar rocks, it is shown that mare regolith is enriched in aluminum and depleted in iron, titanium, and chromium. This effect cannot be accounted for only by the admixture of highland anorthositic material. The entire array of geochemical data points to the considerable role of depth-wise differentiation of the magmatic material in forming the composition of the primary lunar rocks and, naturally, the composition of the regolith. During regolith formation, processes of the effervescing of magma as it outflowed at the lunar surface were of primary importance. Impacts by micrometeorites represent another important factor.
Carbon compounds composition and origin in Apollo 11 lunar samples using pyrolytic chromatography and microscopy at elevated temperature