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Lindsley, D. H.

Publications and source records attributed to Lindsley, D. H..

Mare glasses from Apollo 17 - Constraints on the moon's bulk composition

Two previously unreported varieties of mare volcanic glass have been discovered in Apollo 17 samples. Twenty-three chemical types of volcanic glass have now been analyzed from the six Apollo landing sites. These volcanic glasses, which may be samples of primary magmas derived from the differentiated lunar mantle, define two linear arrays that seem to reflect regional, if not global, regularities among the source regions of these melts. Additional systematics among these glasses have been used to estimate the bulk composition of the moon. The results suggest that the refractory lithophile elements are present at abundances of 1.7 x chondrites. The silicate portion of the moon appears to have a major-element composition similar to a volatile (Si, Na, K)-depleted, earth's upper mantle. The theory involving an earth-fission origin of the moon can be tested further through trace element analyses on the volcanic glasses, and through determination of the N/Ar-36 ratio and noble gas isotopes from primordial lunar gas trapped within vesicles associated with mare volcanic glass.

Delano, J. W.

Apollo 14 very low titanium glasses - Melting experiments in iron-platinum alloy capsules

This paper describes two techniques that have been developed to produce Fe-Pt alloy capsules for hgh-pressure experiments, and reports liquidus-phase relations of the Apollo 14 very low titanium glasses determined using Fe-rich capsules (a/Fe/ approximately 0.6). The liquid is multiply saturated with olivine and clinopyroxene at equal to or greater than 22 kbar. The multiple saturation is at least 3 kbar higher than that determined using pure Fe capsules and corresponds to a source region at least 60 km deeper if olivine and clinopyroxene were the residual phases. However, independent data on iron activity or oxygen fugacity of the glasses are still needed in order to choose a container of optimum composition. Preliminary experiments in Fe-poor alloy capsules suggest that the valence state of iron and the crystallization sequence in the melt have changed, possibly as a result of oxidizing materials entrapped during the iron-plating processes. The FeO content of the charge decreases linearly with increasing run duration in experiments using pure Fe capsules. The observation that iron-rich globules grow with time suggests that the equilibrium Fe (bleb) + Fe2O3 (liq) = 3 FeO (liq) might be established in the liquid at high pressure. If this explanation is correct, an appreciable amount of 'FeO' in the liquid could actually be Fe2O3, and some natural lunar volcanic glasses may contain ferric iron as well.

Chen, H.-K.

A two-pyroxene thermometer

Experimentally determined pyroxene phase relations at 800-1200 C are combined with calculated phase equilibria for the Di-En and Hd-Fs joins to yield a graphical two-pyroxene thermometer that should be suitable for a wide variety of rocks from the earth, the moon, and meteorites. The thermometer can be used directly with natural pyroxenes having low contents of Al and other minor components. Samples having higher contents of 'other' components require special projection onto the Ca-Mg-Fe pyroxene quadrilateral; Wo, En, and Fs as normally calculated will not yield correct temperatures. The special projection is required to approximate the activities of those components in natural pyroxenes. Whereas the effects of pressure are nonnegligible, they can be corrected for. It is pointed out that use of the thermometer for slowly cooled rocks may pose special problems if the pyroxenes have undergone granule exsolution (coalescence of exsolved material to form separate grains).

Lindsley, D. H.

Chemical systematics among the moldavite tektites

The compositional variations that occur among the moldavite tektites are caused principally by incomplete mixing of two components during fusion. With the possible exception of silica, there is no evidence for significant losses of volatile species by fractional vaporization. Chemical constraints have been calculated for the two source-materials that contributed to the moldavites. If these tektites were formed by impact fusion, as is commonly believed, then the compositional systematics preserved within the moldavites suggest that hypersonic flow and ejection of impact melts are orderly processes. Insights gained from the study of tektites should prove useful in interpreting the chemistries of impact glasses from other bodies in the solar system.

Delano, J. W.

Glasses of impact origin from Apollo 11, 12, 15, and 16 - Evidence for fractional vaporization and mare/highland mixing

Electron microprobe analyses have been performed on glasses of impact origin in Apollo 11 breccias (10059, 10060, 10061), Apollo 12 soil (12070), and Apollo 15 breccias (15318, 15425, 15426, 15427). These glasses were produced by shock melting of regolith, rather than of rock. Simple concepts for better understanding and interpreting the chemical data from impact glasses have been developed. These concepts are a significant improvement on earlier strategies, which centered principally on cluster analysis. Using ratios of refractory lithophile elements, the compositional effects of fractional vaporization often associated with impact melting to obtain chemical information about the mare and highland components in the regoliths parental to the glasses have been 'seen through'. This method is also applied to the mare-derived impact glasses from Apollo 16 in order to place constraints on the types of volcanic components occurring in Mare Nectaris. Since impact glasses can be used to derive chemical constraints on the indigenous lithologies comprising multi-component regoliths; the frequent occurrence of these glasses, as well as their low masses, should make them critically important for study when small quantities of grab-samples are returned by future unmanned spacecraft from planets, satellites, and asteroids where regoliths are present.

Delano, J. W.

The Apollo 15 yellow impact glasses - Chemistry, petrology, and exotic origin

The Apollo 15 yellow impact glasses are characterized by moderate TiO2 (about 4.8%) and high abundances of the large ion lithophile elements (e.g., K, P, Hf, Th, REE). Since the chemistry of these glasses cannot be duplicated by any combination of local components presently known to occur at the Apollo 15 landing site, these yellow glasses seem to be exotic to that area. Chemical and petrologic constraints suggest that these samples were produced by impact melting of an immature mare regolith developed upon an unusual variety of mare basalt. It is speculated that the target basalts were the youngest lava flows known to exist on the moon (i.e., Eratosthenian-age lavas in Oceanus Procellarum and Mare Imbrium). Specific tests are proposed for evaluating this provocative hypothesis.

Delano, J. W.

Chemistry and phase relations of VLT volcanic glasses from Apollo 14 and Apollo 17

The VLT (very low titanium) volcanic glasses from Apollo 14 and Apollo 17 have been analyzed for the major elements and trace Ni. These glasses display compositional trends that may not result entirely from olivine fractionation. The phase relations have been determined experimentally. Olivine is the liquidus phase in the pressure interval from 0 to about 18 kbar. Pigeonite is the liquidus phase from about 18 kbar to 22 kbar or more. If these VLT volcanic glasses are samples of primary melts that had been in chemical equilibrium with olivine and low-Ca pyroxene in their source regions, then these liquids were derived from depths of 360-380 km within the moon.

Chen, H.-K.

A valid Margules formulation for an asymmetric ternary solution - Revision of the olivine-ilmenite thermometer, with applications

A derivation of a valid asymmetric ternary Margules expression for the excess free energy is presented, and the olivine-ilmenite thermometer is revised accordingly. Although the effect on the thermometer is relatively small, the revision results in improved precision. Estimated temperatures of equilibration are presented for olivine and ilmenite from lunar and terrestrial rocks.

Andersen, D. J.

The olivine-ilmenite thermometer

It is noted that the partitioning of Fe(2+) and Mg between olivine and ilmenite is temperature-dependent and can serve as a geothermometer if the activity-composition relations are determined. The paper reports on the study of the partitioning from 700-980 C at 1 kbar and 800-900 C at 13 kbar, and develops a solution model to account for the nonideality of olivine in the binary system fosterite-fayalite and for ilmenite in the ternary system ilmenite-geikielite-hematite. A comparison with crystallization experiments shows that this thermometer may be safely extrapolated to temperatures higher than those of the exchange experiments.

Andersen, D. J.

Mare basalt petrogenesis - A review of experimental studies

Experimental results relevant to the fundamental question of the origin of mare basalts are examined with particular reference to guidelines for an appropriate evaluation of experiments. The petrogenesis of mare basalts remains a controversial subject as no petrogenetic scenario has yet been able to satisfy all the geochemical and geophysical constraints. Several generalizations hold true if one accepts that high-pressure equilibria provide some useful but limited information on mare source regions in the lunar interior. Petrogenesis of lowand high-Ti suites is identified. If assimilative processes are involved in the petrogenesis of the high-Ti suite, the high-pressure experiments on the resultant hybrid liquids have little bearing on their origins.

Kesson, S. E.

The effects of Al/3+/, Cr/3+/, and Ti/3+/ on the stability of armalcolite

Experimental studies on the binary system FeTi2O5-MgTi2O5 yield unrealistically high values for the lower thermal stabilities of lunar armalcolites, since these typically contain 10-15 mole% (Al, Cr, Ti/3+/)2TiO5 components. Pure binary Fe0.5Mg0.5Ti2O5 begins to break down at 1010 + or - 20 C whereas Fe0.5Mg0.5Ti2O5)0.85(Ti2/3+/TiO5)0.15 persists to approximately 900 C and (Fe0.5Mg0.5Ti2O5)0.84(Al2TiO5)0.04(Cr2TiO5)0.03(Ti2/3+/TiO5)0.09 (a model Apollo 17 armalcolite) remains stable down at least to 850 C. The lower thermal stability of the model Apollo 17 armalcolite is raised by approximately 35 C per kilobar of load pressure. The breakdown curve intersects the solidus of likely source materials for high-Ti lunar basalts at 9-10 kbar; thus, the maximum depth at which this armalcolite is stable is 180-200 km. Subsolidus isochemical reaction of Ti/3+/ and Fe/2+/ components in armalcolite can yield rutile and metallic Fe. This assemblage could be misidentified as due to an externally imposed reduction.

Kesson, S. E.

Mare basalts from the Taurus-Littrow region of the moon

Two distinct chemical basalt types have been sampled at the Apollo 17 landing site. Very high-titanium basalts (about 13 wt % TiO2) are the dominant type and display a textural range from olivine-porphyritic, ilmenite vitrophyres to plagioclase-poikilitic, ilmenite microgabbros. Most of these rocks could have come from one flow. These basalts appear to represent partial melts from feldspar-ilmenite cumulates with an Ar-40/Ar-39 age of about 3.7 G.y., which have experienced little, if any, near-surface fractionation of olivine and Fe-Mg-Ti oxides. A second type of basalt virtually identical to the Apollo 11 (low-K) basalts is much less common.

Papike, J. J.

The stability of armalcolite - Experimental studies in the system MgO-Fe-Ti-O

The stability of armalcolite at low pressures is considered, taking into account experiments which confirm the low-temperature breakdown of the mineral. Effects of Al2O3, Cr2O3, and Ti2O3 components on armalcolite stability are discussed with the stability of armalcolite at high pressure. Attention is also given to several reactions involving Fe-Mg-Ti oxides in Apollo 11 and 17 basalts.

Lindsley, D. H.