Search NASASearch

Engineering topics

Hewins, R. H.

Publications and source records attributed to Hewins, R. H..

At least 19 records

Tin Abundances Require that Chassignites Originated from Multiple Magmatic Bodies Distinct from Nakhlites

Meteorites from Mars lack field context but chemical and chronologic studies have revealed remarkable links between nakhlites and chassignites. A widely held consensus is that nakhlites and chassignites originated from a large, single differentiated flow or shallow intrusive [1-5]. An Ar-Ar study assumed multiple flows based on resolvable age differences between meteorites [6], but did not address the possibility of differential cooling in a large, shallowly emplaced intrusion [1]. REE abundances in pyroxenes from nakhlites and Chassigny led [7] to argue for derivation of these rocks from distinct magmas. Volatile abundances (F, Cl, OH) in chlorapatites indicated that the entire suite of nakhlites and chassignites experienced hydrothermal interaction with a single fluid supporting a single body origin [4]. The discovery of a new chassignite, NWA 8694, extended the Mg# range from 80-54, providing a closer link to nakhlites but revealed the petrological difficulty of fractionating a single body of liquid to yield a series of olivine cumulates with such a large Mg# range [8]. When mafic magmas are emplaced into the crust, crustal assimilation can impart distinct elemental signatures if the country rock has experienced sedimentary or hydrothermal processing [9]. In this work, we used Sn abundances of nakhlites and chassignites to show that these rocks were crystallized from distinct magma batches, providing vital contextual clues to their origin.

Humayun, M.

Chalcophile Element Constraints on the Sulfur Content of the Martian Mantle

The sulfur content of the Martian mantle is critical to understanding volcanic volatiles supplied to the surface of Mars and possibly climate. In the absence of Martian mantle rocks, sulfur content of the mantle has been inferred from S contents of Martian meteorites or from sedimentary sulfate abundances. Estimates of the sulfur content of the Martian mantle vary from 390-2,000 ppm, all of which are higher than that of the terrestrial mantle (~250 ppm;). Residual sulfide in the Martian mantle controls the distribution of chalcophile elements during partial melting. In this study, we report new analyses of Martian meteorites, and use the incompatible behavior of As, Tl and Pb to infer the sulfide mode of the Martian mantle using a different set of assumptions than those of prior studies.

Yang, S.

A Two Gigayear History of Germanium Outgassing from Shergottites

Germanium (Ge) and Zn enrichment in martian sedimentary rocks has been reported from rocks at Gale Crater, showing concentrations of Ge from tens to hundreds ppm [1]. The Ge concentrations in martian meteorites are significantly lower (0.5-2.5 ppm) [2]. Our recent studies [3-4] have revealed that Ge is lost from shergottites due to volatility. Recent experimental studies confirm that Ge and Zn are both significantly volatile under magmatic conditions [5-7]. Further, Ge is moderately incompatible during magmatic differentiation [8] so Ge contents in olivines or pyroxenes increase during igneous fractionation in nakhlites and chassignites [4]. Shergottites for which Ge abundances had been determined included rocks with ages of 150-600 Ma, while the enrichments reported from Gale Crater rocks likely occurred over 3 Ga ago. The recent discovery of two unpaired ancient (2.4 Ga) depleted shergottites, NWA 7635 [9] and NWA 8159 [10], afforded the prospect of obtaining an extended history of martian volcanic outgassing. Both of the ancient shergottites are depleted in incompatible elements and share a similar GCR exposure age to younger depleted shergottites implying derivation from a single, long-lived (>2 Ga) volcanic center [9].

Yang, S.

The Germanium Dichotomy in Martian Meteorites

Germanium is a moderately volatile and siderophile element that follows silicon in its compatibility during partial melting of planetary mantles. Despite its obvious usefulness in planetary geochemistry germanium is not analyzed routinely, with there being only three prior studies reporting germanium abundances in Martian meteorites. The broad range (1-3 ppm) observed in Martian igneous rocks is in stark contrast to the narrow range of germanium observed in terrestrial basalts (1.5 plus or minus 0.1 ppm). The germanium data from these studies indicates that nakhlites contain 2-3 ppm germanium, while shergottites contain approximately 1 ppm germanium, a dichotomy with important implications for core formation models. There have been no reliable germanium abundances on chassignites. The ancient meteoritic breccia, NWA 7533 (and paired meteorites) contains numerous clasts, some pristine and some impact melt rocks, that are being studied individually. Because germanium is depleted in the Martian crust relative to chondritic impactors, it has proven useful as an indicator of meteoritic contamination of impact melt clasts in NWA 7533. The germanium/silicon ratio can be applied to minerals that might not partition nickel and iridium, like feldspars. We report germanium in minerals from the 3 known chassignites, 2 nakhlites and 5 shergottites by LAICP- MS using a method optimized for precise germanium analysis.

Humayun, M.

Compound chondrules: An experimental investigation

Compound chondrules are considered to be the product of collisions between molten chondrules during chondrule formation Wasson, J. T. et al. (1994) have argued that some compound chondrules are formed when a chondrule with an accretional rim experienced a flash-melting event similar to a chondrule-forming event. We have designed experiments to investigate the formation of compound chondrules by both methods. Experiments were performed on a Deltech vertical muffle tube furnace to form synthetic chondrules to use as accretion rim material. For our experimental conditions, it is clear that compound chondrules can only be made by a collisional event. Our changes maintain their spherical shape and produce distinct boundaries between charges that are similar to natural compound chondrules. Furthermore, collision event(s) between chondrules will cause nucleation if they are molten and undercooled, thus producing chondrule textures. Flash melting chondrules with accretionary rims will not produce compound chondrules but will produce new chondrules with new textures.

Connolly, H. C., Jr.

Constraints placed on the nature of chondrule precursors

The melting conditions and cooling rates experienced by chondrules have been experimentally investigated and reviewed. A discussion of experiments that have studied the nature of chondrule precursors and what constraints these experiments have placed on chondrule precursors is presented. Topics discussed include the following: (1) physical characteristics of starting compositions; (2) chemical characteristics of starting compositions; and (3) constraints on chondrule precursors.

Connolly, H. C., Jr.

Experimental constraints on models for origins of chondrules: Peak temperatures

Chondrule peak temperature constraints for mathematical models pertaining to chondrule origin are discussed in this article. The peak temperatures experienced by chondrules provide a parameter that may allow discrimination between alternative heating mechanisms. Successful mechanisms must provide just enough energy to reach such temperatures and not overshoot them. In principle, determination of peak temperatures from chondrule textures and experiments that duplicate them should be very easy. However, this approach is complicated by the fact that there are several different experimental paths that reproduce chondrule properties. The key texture depends not only on the peak temperature but also on the heating time and, in the case of totally molten droplets, on interactions with other particles. Addressed here are different types of peak temperature constraints; (1) near-liquidus melting; (2) flash melting; (3) dust seeding; (4) volatile element constraints; and (5) barred olivine chondrules.

Hewins, R. H.

Flash heating is required to minimize sodium losses from chondrules

Chondrules were formed by high-temperature melting events, but do not always show Na depletion compared to CI chondrites, though extensive Na loss has been found in previous isothermal experiments. While Na loss can be prevented by high partial pressure of Na in the nebula, many people favor a flash-heating mechanism to reduce the Na loss from chondrule melts. To examine the validity of the flash-heating hypothesis, we have conducted a series of flash-heating experiments and observed Na loss rate under different conditions. Our results support the flash heating as a plausible heating mechanism to form chondrules.

Yu, Y.

Chondrule precursors and cooling paths: The sulfur evidence

The behavior of moderately volatile elements (Na and S) is controversial but critical in understanding chondrule precursors and heating processes. Sulfide appeared to be present in most chondrules, but S should have been vaporized during chondrule formation. In fact, S is extensively redistributed in the course of metamorphism, and its abundance at the end of chondrule formation can only be inferred from the least equilibrated chondrites. Our study of 530 chondrules from Renazzo (CR2) and Semarkona (LL3.0) shows partial volatilization of S during chondrule formation and our melting experiments define conditions for total loss or partial retention of S.

Zanda, B.

Mineralogy, petrology and geochemistry of carbonaceous chondritic clasts in the LEW 85300 polymict eucrite

We have performed a detailed petrologic and mineralogic study of two chondritic clasts from the polymict eucrite Lewis Cliff (LEW) 85300, and performed chemical analyses by INAA and RNAA on one of these. Petrologically, the clasts are identified and are composed of dispersed aggregates, chondrules, and chondrule fragments supported by matrix. The aggregates and chondrules are composed of olivine, orthopyroxene, plus some diopside. The matrix consists of fine-grained olivine, and lesser orthopyroxene and augite. Fine-grained saponite is common in the matrix. The bulk major composition of the clast studied by INAA and RNAA shows unusual abundance patterns for lithophile, siderophile and chalcophile elements but is basically chondritic. The INAA/RNAA data preclude assignment of the LEW 85300,15 clast to any commonly accepted group of carbonaceous chondrite.

Zolensky, M. E.

Igneous activity in the early solar system

Although the main emphasis of this book is on what can be learned about the early solar system from material that has escaped secondary processing, the study of differentiated meteorites can provide unique insights into the processes of basalt generation and core formation. Such processes would have been of fundamental importance during the evolution of planetary objects, including the terrestrial planets, early in solar-system history. The properties of igneous meteorites are studied with attention given to the howardite-eucrite-diogenite (HED) suite. Geochemical and petrologic trends in those meteorites are discussed with the objective of defining the thermal and chemical evolution of the HED parent body. A major issue is the nature of the dominant source of heat in the early solar system.

Hewins, R. H.

Experimental studies of chondrules

A series of dynamic crystallization experiments has been conducted with several chondrule compositions. The results obtained have demonstrated that the many heterogeneous nuclei control chondrule textures. The presence of a few nuclei thus leads to barred and radiating textures from melts at or above liquidus; several nuclei just below liquidus result in microporphyritic textures; and spherules cooled faster than 2000 C/hr develop more spherulitic or acicular crystals than those of typical chondrules. The dominance of granular textures in Mg-rich olivine chondrules, porphyritic textures in Fe-rich olivine chondrules, and radiating textures in Si-rich chondrules, indicates a common limit to the initial temperature.

Hewins, R. H.

Melt segregation in plagioclase-poikilitic mesosiderites

The Budalan and Mincy mesosiderites contain a poikilitic-plagioclase matrix with orthopyroxene chadacrysts and interstitial-subophitic inverted pigeonite. Orthopyroxene chadacrysts in both mesosiderites are uniformly more aluminous than orthopyroxene clasts, suggesting that they were not derived from clasts by metamorphism. Interstitial inverted pigeonite is more ferroan than adjacent orthopyroxene in the matrix, consistent with the crystallization of a melt with the sequence orthopyroxene followed by pigeonite. The magnesium chadcrysts in Mincy could not have formed from a melt in equilibrium with the clasts but could have crystallized from impact melt. The most Mg chadacrysts are enclosed in large reversely zoned plagioclase crystals as a result of the undercooling in melt-lacking plagioclase clasts and associated nuclei. Mincy contains both plagioclase-poor and plagioclase-rich regions, explained by a separation of silicate melt into pools. Reckling Peak A80258, a plagioclase-poikilitic mesosiderite with a very high chadacryst/plagioclase ratio, resembles Mincy material from which melt has been extracted. It is suggested that the origin of the plagioclase-poikilitic mesosiderites is impact melting of a metal-silicate mixture.

Hewins, R. H.

The case for a melt matrix in plagioclase-POIK mesosiderites

Reasons are given for reclassifying former 'poikiloblastic' mesosiderites as 'poikilitic' in order to better represent their thermal histories. Attention is focused on the plagioclase-POIK mesosiderites Bondoc, Budulan, and Mincy, which all display silicate melt matrices similar to the Palisades sill and Apollo 17 mare basalts. The poikilitic textures, resorbed olivine grains, and the crystallization sequence are sufficient to reclassify the three specimens from 3B to 4B mesosiderites. Because the 4B mesosiderites are clast-laden melt rocks, their origins were probably in impact melts, which would have combined hot melts with cold clasts.

Hewins, R. H.

Intrinsic oxygen fugacities of diogenites and mesosiderite clasts

Oxygen fugacities of diogenite and mesosiderite clast material were measured with the double ZrO2 cell technique between 800 and 1150 C. The samples were taken from large clasts in the diogenites Johnstown (En73) and Tatahouine (En75), and the mesosiderites Estherville (En81), West Point (Fo88) and Emery (En68). Fugacity values for all except Emery plot near the wuestite-iron buffer curve and are interpreted as indicating similar source regions and environments of crystallization for the two suites. Emery orthopyroxene records a lower fugacity, close to the fayalite-quartz-iron buffer curve, probably as a result of equilibration with the mesosiderite matrix assemblage. The similarity of redox conditions experienced by mesosiderite orthopyroxenite and diogenites is not sufficient to require a single parent body and, if the common achondrites were derived from Vesta, mesosiderites probably came from a different body.

Hewins, R. H.

Processes and subdivisions in diogenites, a multivariate statistical analysis

Multivariate statistical techniques used on diogenite orthopyroxene analyses show the relationships that occur within diogenites and the two orthopyroxenite components (class I and II) in the polymict diogenite Garland. Cluster analysis shows that only Peckelsheim is similar to Garland class I (Fe-rich) and the other diogenites resemble Garland class II. The unique diogenite Y 75032 may be related to type I by fractionation. Factor analysis confirms the subdivision and shows that Fe does not correlate with the weakly incompatible elements across the entire pyroxene composition range, indicating that igneous fractionation is not the process controlling total diogenite composition variation. The occurrence of two groups of diogenites is interpreted as the result of sampling or mixing of two main sequences of orthopyroxene cumulates with slightly different compositions.

Harriott, T. A.

Impact versus internal origins for mesosiderites

The textures, mineral compositions, and thermal history of mesosiderites are examined to see whether they are compatible with any kind of impact process or internal process which might produce stony-iron breccias. It was proposed that cratering by metal projectiles is not an adequate origin mechanism since it would not deposit enough metal in the stony-iron breccias. It was also proposed that such mechanisms as accretion of differentiated planitesimals must be considered for mesosiderite origins. But no single model for origins is fully satisfactory. Disruption and reassembly of two colliding bodies could form stony-iron breccias at depth, but, as with the previous models, the easiest way to explain the low olivine of mesosiderites is to postulate derivation from olivine-poor chondritic material. Turbulent metal-crust mixing during core formation and crustal blocks sinking into the core withhold olivine from the breccia but do not explain how the silicate and metal liquids in subgroup IV could have failed to segregate.

Hewins, R. H.