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Pillinger, C. T.

Publications and source records attributed to Pillinger, C. T..

At least 37 records · Page 2

Are the C delta light nitrogen and noble gases located in the same carrier?

Light nitrogen and the HL family noble gas components of C(sub delta) appear to be separable by high resolution pyrolysis experiments. Thus C(sub delta) is not a homogeneous material and probably consists of debris of many stars. The question of whether the N and Xe(HL) actually reside in different carriers continues to be addressed. It is well known that C(sub delta) which was identified as nanometer sized diamonds contains isotopically anamalous elements, in particular noble gases including Xe(HL) and its family and light nitrogen (delta(N-15) down to -350 percent). Before the true nature of C(sub delta) was recognized, it was easy to suppose that the Xe(HL) and light nitrogen were located in the same carrier. However, recognition that light nitrogen in diamond from different samples varies by greater than a factor of six compared to Xe(HL) fluctuations of ca. 20 percent makes such an assumption questionable. On the basis of simple arithmetic logic, the Xe and nitrogen cannot be absolutely co-located. The average diamond grain consists of only about 1000-2000 atoms of carbon; one grain among a few x 10(exp 6) contains an atom of Xe(HL) while 5-30 atoms of light nitrogen are the typical number which need to be in every diamond grain to account for observed concentrations. If some grains are devoid of N, the others have to have a higher N concentration. Even if we were able to analyze an individual grain of the diamond for noble gases and nitrogen, we would be faced with the monumental task of locating the one amongst 10(exp 6) identical grains containing the Xe atom to examine its nitrogen content. The problem can be simplified to some extent if instead of Xe, He which is 10(exp 4) times more abundant is assumed to be a member of the HL family. Attempts to fractionate the separate carriers might be attempted using He and N as guiding indicators but even experiments of this nature are for the future. Faced with apparently insoluble problems, we have returned to an investigation we last used in our original efforts to find isotopically light nitrogen, that is to compare release patterns of the different components during stepped pyrolysis and combustion.

Verchovsky, A. B.↗

The carbon components in SNC meteorites of feldspathic harzburgite composition

Two meteorites collected in Antarctica, ALH A77005 and LEW 88516, have characteristics which link them to the shergottite group of SNC meteorites. Essentially, ALH A77005 and LEW 88516 are feldspathic harzburgites, being comprised of roughly equal quantities of olivine and pyroxene, with an additional few percent of feldspar which has subsequently been converted to maskelynite by shock. The meteorites represent samples of a cumulate rock which is itself composed of two different lithologies: in one, large pyroxenes poikilitically enclose olivine crystals, while the other consists of interstitial areas made up of pyroxene, olivine, maskelynite, whitlockite, troilite, ilmenite and chlorapatite. It has been proposed that meteorites such as ALH A77005 (and LEW 88516) are relict samples of the source peridotite from which the other shergottites formed. As such it should be informative to study in detail the carbon components present within these samples, in order to make comparisons with data from other shergottites. Although not plutonic in origin, and therefore not sampling a truly deep source, analyses of ALH A77005 and LEW 88516 should assist with attempts to define the bulk carbon isotopic composition of Mars. This has been assessed previously through analyses of carbon of presumed magmatic origin in other SNC meteorites, but the carbon isotopic compositions obtained seem to be at variance with what might be expected. It is important to constrain the carbon isotopic composition of Mars as well as possible so that models of atmospheric evolution, based on carbon isotopic data, can yield the most reliable results.

Wright, I. P.↗

Further carbon isotope measurements of LEW 88516

Douglas et al. have previously analyzed the carbon content and isotopic composition of a crushed sample (sub-sample 13) of the shergottite, LEW 88516. The powder, which was from a relatively large portion of the meteorite in order to obtain a representative sample, was distributed amongst the scientific community. However, it is probable that the preparation procedure was not optimized for the purposes of carbon measurements. Indeed, it was found that LEW 88516,13 contained over 1200 ppm carbon, a concentration which is greater than that present in any other SNC meteorite. That a close relative, ALH A77005, contains only 141 ppm carbon seems to implicate the preparation procedure as being responsible for the apparently high carbon content of LEW 88516. However, it may also be the nature of the fine powder which has resulted in contamination. The observation of high carbon content in LEW 88516,13 highlights the extreme difficulty of trying to obtain representative samples of whole meteorites for this kind of investigation. Presented herein are some further measurements of LEW 88516 which should serve to clarify some of the issues raised by the previous investigation.

Wright, I. P.↗

An attempt to comprehend Martian weathering conditions through the analysis of terrestrial palagonite samples

Spectroscopic observations of the Martian surface in the invisible to near infrared (0.4-1.0 micron), coupled with measurements made by Viking, have shown that the surface is composed of a mixture of fine-grained weathered and nonweathered minerals. The majority of the weathered components are thought to be materials like smectite clays, scapolite, or palagonite. Until materials are returned for analysis there are two possible ways of proceeding with an investigation of Martian surface processes: (1) the study of weathering products in meteorites that have a Martian origin (SNC's), and (2) the analysis of certain terrestrial weathering products as analogs to the material found in SNC's, or predicted to be present on the Martian surface. We describe some preliminary measurements of the carbon chemistry of terrestrial palagonite samples that exhibit spectroscopic similarities with the Martian surface. The data should aid the understanding of weathering in SNC's and comparisons between terrestrial palagonites and the Martian surface.

Douglas, C.↗

Carbonates, surfates, phosphates, nitrates, and organic materials: Their association in a Martian meteorite

The debate concerning the evolution of CO2 on Mars continues. It would appear that in order to explain the valley networks and other relict fluvial landforms it is necessary to accept that liquid water was once present at the surface of Mars. This in turn requires, at some point in the planet's history, a higher surface temperature than exists today, proposition explained traditionally by an early dense CO2, atmosphere. However, there are a number of problems with this notion: for instance, CO2 alone is not an efficient greenhouse gas because of its tendency to form clouds. Moreover, if there was an early dense CO2 atmosphere, it is necessary to explain where the elemental constituents now reside. There are two possibilities for the latter, namely loss to outer space of atmospheric CO2 or the formation of vast carbonate deposits. While some models of atmospheric loss predict that up to 0.4 bar of CO2 could be removed from the Martian surface, this is still not enough to account for the original atmospheric inventory, usually considered to have been in the range of 1-5 bar. Thus, most models of the evolution of the Martian surface require removal of CO2 from the atmosphere and into carbonate deposits. However, as yet, the evidence for the existence of carbonates on Mars is fairly scant. This is an issue that would have been resolved by results obtained from Mars Observer.

Wright, I. P.↗

Attempts to comprehend Martian surface processes through interpretation of the oxygen isotopic compositions of carbonates in SNC meteorites

The SNC meteorites are known to contain trace quantities of a variety of secondary minerals such as carbonates, sulfates, and aluminosilicates. Since these constituents are thought to be mostly preterrestrial in origin, their study has the potential to provide rigorous constraints on the nature of martian weathering processes. However, this line of investigation is potentially complicated by the presence within the meteorite samples of any additional weathering products produced by terrestrial processes. Examination of such terrestrial components is important since weathering processes that affect meteorite samples following their fall to Earth might have some bearing on the nature of analogous processes at the surface of Mars. It is obviously necessary to try and distinguish which secondary components in SNC meteorites are terrestrial in origin from those that are preterrestrial. Herein consideration is made of the stable isotopic compositions of weathering products in two SNC meteorites: EET A79001 (a sample collected from Antarctica) and Nakhla (a fall from Egypt, 1911).

Wright, I. P.↗

Martian surficial carbon-constraints from isotopic measurements of shock-produced glass in EET A79001

At the highest temperatures of extraction, trapped Martian atmospheric CO2 is released. For this component, delta C-13 rises to +27 percent (compared to +15 percent previously). Because of the possibilities that C-13 rich atmospheric CO2 is released along with C-13 depleted crustal carbon, the highest delta C-13 value measured represents a lower limit to the true isotopic composition of the atmospheric species. Thus, the new delta C-13 determination is considered to best represent Martian atmospheric CO2. Based on a delta C-13 of +27 percent, and a release temperature of 1000-1200 C, the new analysis shows the glass to contain 2.4 ppm C as CO2, compared to 5.5 ppm C previously. Thus, it would seem that trapped CO2 is distributed rather unevenly throughout the glass.

Wright, I. P.↗

The stable isotopic compositions of indigenous carbon-bearing components in EETA 79001

It is now widely accepted that the most likely source of SNC meteorites is Mars. An oblique impact on Mars, or vaporization of permafrost, by an impactor seem to be the most likely ejection mechanisms capable of accelerating material to the 5 km/s velocity needed to overcome the gravitational field of Mars. These ejection mechanisms involve a large shock event in the SNC class, the shergottites EETA 79001 and ALHA 77055 are the most likely shocked samples, in which whole rock pressures of 35 to 45 GPa have been estimated. Martian weathering products have also been identified in EETA 79001. Here, the author started a series of analyses of EETA 79001 using a high-sensitivity static mass spectrometer capable of measuring sub-nanogram quantities of carbon. Recent measurements of lithology C confirm that the shock-implanted atmospheric CO2 is released during the 1100 to 1200 C step.

Hartmetz, C. P.↗

On the isotopic composition of magmatic carbon in SNC meteorites

SNC meteorites are thought, from many lines of evidence, to come from Mars. A line of investigation which has been pursued in our laboratory over the years involves measurement of the stable isotopic composition of carbon, in its various forms, in SNC meteorites. In order to establish a firm basis for studying the isotopic systematics of carbon in the martian surface environment, it is first necessary to try and constrain the delta C-13 of bulk Mars. Taking all of the available information, it would seem that the delta C-13 of the Earth's mantle lies somewhere in the range of -5 to -7 percent. Preliminary assessment of magnetic carbon in SNC meteorites, would tend to suggest a delta C-13 of 20 to 30 percent, which is conspicuously different from that of the terrestrial mantle. It is not obvious why there should be such a difference between the two planets, although many explanations are possible. One of these possibilities, that previous delta C-13 measurements for magnetic carbon in SNC meteorites are in error to some degree, is being actively investigated. The most recent results seem to constrain the theta C-13 of the magnetic carbon in SNC meteorites to about -20 percent, which is not at odds with previous estimates. As such, it is considered that a detailed investigation of the carbon isotopic systematics of martian surface materials does have the necessary information with which to proceed.

Wright, I. P.↗

Xylan - A potential contaminant for lunar samples and Antarctic meteorites

The possibility that lunar samples have been contaminated by the proprietary lubricant paint known as Xylan, which has been applied to screw threads in dry-N sample processing cabinets at NASA JSC, is considered. From a sample analysis using sealed-tube and stepped combustion, it is argued that the unexpectedly high concentration of organic materials found in EET A79001 is not due to Xylan contamination. It is considered unlikely that previous C and N analyses of lunar samples have been affected by the introduction of Xylan.

Wright, I. P.↗

The formation of weathering products on the LEW 85320 ordinary chondrite - Evidence from carbon and oxygen stable isotope compositions and implications for carbonates in SNC meteorites

Isotopic analysis of nesquehonite recovered from the surface of the LEW 85320 H5 ordinary chondrite shows that the delta C-13 and delta O-18 values of the two generations of bicarbonate (Antarctic and Texas) are different: delta C-13 = + 7.9 per mil and + 4.2 per mil; delta O-18 = + 17.9 per mil and + 12.1 per mil, respectively. Carbon isotopic compositions are consistent with equilibrium formation from atmospheric carbon dioxide at - 2 + or - 4 C (Antarctic) and + 16 + or - 4 C (Texas). Oxygen isotopic data imply that the water required for nesquehonite precipitation was derived from atmospheric water vapor or glacial meltwater which had locally exchanged with silicates, either in the meteorite or in underlying bedrock. Although carbonates with similar delta C-13 values have been identified in the SNC meteorites EETA 79001 and Nakhla, petrographic and temperature constraints argue against their simply being terrestrial weathering products.

Grady, Monica M.↗

Stable isotopic studies of H,C,N,O and S in samples of Martian origin

The present day geochemical cycles of volatile elements through the various reservoirs on Earth are largely understood within the context of the planet's standing as a geologically and biologically evolved body. In terrestrial studies stable isotope measurements of light elements (H, C, N, O and S) can be utilized to obtain insight into the conditions prevailing during formation of rocks of various types. Perhaps the most important problem which could be addressed by light element studies of the sorts of specimen likely to be available from remote automatic sampling, would be the role of volatiles during evolution. Of fundamental importance here is the question of whether Mars was volatile rich or volatile poor. The only way to fully comprehend the effects of volatile cycling through the mantle crust and regolith atmosphere polar cap system of Mars, is by analyses of appropriate returned samples. In order to interpret the record of geological activity in Martian samples it will be necessary to understand how the past, or present, surface environment may have acted to disturb the primary characteristics of the rocks.

Wright, I. P.↗

Nature and origin of C-rich ordinary chondrites and chondritic clasts

The abundance and the isotopic compositions of C, O, and noble gases were investigated together with the petrologic characteristics of four carbon-rich ordinary chondrites (Sharps and Allan Hills A77011, A78119, and A81024) and three C-rich chondritic clasts. The results of the analyses suggest that all of the chondrites and clasts analyzed belong to petrologic type 3 and contain abundant carbon-rich aggregates, which, in at least two of these samples, consist of poorly graphitized carbon commonly associated with metallic Fe,Ni. The data also suggest that the four C-rich chondrites originated on the H, L, and LL parental bodies, but that clasts in Dimmitt and Plainview and other regolith breccias may come from different bodies. The results obtained are consistent with the view that graphite is not a common nebular phase.

Scott, E. R. D.↗

Earth's early atmosphere as seen from carbon and nitrogen isotopic analysis of Archean sediments

The origin and evolution of the Earth's early atmosphere has long been a topic of great interest but determination of actual compositions over geologic time is a difficult problem. However, recent systematic studies of stromatolite deposits (Precambrian Paleobiology Research Group) has extended our knowledge of Archean ecosystems. It has been shown that many stromatolite deposits have undergone negligible alteration since their time of formation. The discovery of primary fluid inclusions within unaltered 3.5 b.y. old Archiean sediments and the observation that the 3.3 b.y. old Barberton cherts have remained closed to argon loss and have not been subjected to thermal metamorphism suggests that an opportunity exists for the direct measurement of the volatile constituents present at their time of formation. Of primary interest to this study was the possibility that the stromatolites and other Archean sediments might retain a vestige of the atmosphere and thus afford an indication of the variations in carbon dioxide and nitrogen isotopic compositions with time. A suite of essentially unaltered Archean stromatolites and the cherts of different ages and geologic sites have been analyzed for their trapped carbon dioxide and nitrogen compositions by the stepped combustion extraction tech nique utilizing static mass spectrometers for the isotope measurements.

Gibson, E. K., Jr.↗

Lunar nitrogen: Secular variation or mixing?

The two current models to explain the nearly 40% variation of the lunar nitrogen isotopic composition are: (1) secular variation of solar wind nitrogen; and (2) a two component mixing model having a constant, heavy solar wind admixed with varying amounts of indigenous light lunar N (LLN). Both models are needed to explain the step pyrolysis extraction profile. The secular variation model proposes that the low temperature release is modern day solar wind implanted into grain surfaces, the 900 C to 1100 C release is from grain surfaces which were once exposed to the ancient solar wind but which are now trapped inside agglutinates, and the >1100 C release as spallogenic N produced by cosmic rays. The mixing model ascribes the components to solar wind, indigenous lunar N and spallogenic N respectively. An extension of either interpretation is that the light N seen in lunar breccias or deep drill cores represent conditions when more N-14 was available to the lunar surface.

Norris, S. J.↗

Carbon and nitrogen in the deep Earth

High sensitivity mass spectrometric techniques were utilized to study the C-N isotope systematics in basic igneous rocks and mantle materials in an attempt to ultimately constrain the primordial isotopic compositions of these elements and their subsequent fate during the early history of the Earth. Preliminary results obtained for a selection of submarine basaltic glasses and diamonds are summarized concentrating on: (1) the problem of whether isotopes are significantly fractionated during igneous processes; and on (2) the effects of crustal recycling.

Mattey, D. P.↗

Isotopically anomalous nitrogen in primitive meteorites

The extreme enrichement in N-14 (up to 48 percent) found in acid-resistant residues of the Allende and Murchison meteorites cannot be attained by normal solar system processes and must therefore be due to stellar nucleosynthesis. Consequently the xenon component enriched in the heavy isotopes associated with the light nitrogen very probably was made by stellar nucleosynthesis rather than by fission of an extinct superheavy element.

Lewis, R. S.↗

Interstellar carbon in meteorites

The Murchison and Allende chondrites contain up to 5 parts per million carbon that is enriched in carbon-13 by up to +1100 per mil (the ratio of carbon-12 to carbon-13 is approximately 42, compared to 88 to 93 for terrestrial carbon). This 'heavy' carbon is associated with neon-22 and with anomalous krypton and xenon showing the signature of the s-process (neutron capture on a slow time scale). It apparently represents interstellar grains ejected from late-type stars. A second anomalous xenon component ('CCFXe') is associated with a distinctive, light carbon (depleted in carbon-13 by 38 per mil), which, however, falls within the terrestrial range and hence may be of either local or exotic origin.

Swart, P. K.↗