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11.
A newly found polymict eucrite, EETA79006, is described. Lithic clasts are similar to those found in howardites and fall into four groups: fine-grained (aphanitic), coarse-grained, basaltic, and cataclastic. All have eucritic compositions and differ mainly in cooling and deformation histories. Some basaltic clasts cooled faster than others and may be impact melts. Analysis of pyroxene and feldspar in the matrix and in 20 lithic clasts indicates that the matrix was not derived from the observed lithic clast population. This meteorite and similar polymict eucrites may have formed by addition of younger more fractionated lithic clasts to the regolith of the parent body. 相似文献
12.
Abstract— A series of experiments were designed to investigate the textural and compositional changes that take place during disequilibrium partial melting of chondritic material. Chips of the L6 chondrite, Leedey, were heated at 1200 °C and log ?O2 = IW‐1 for durations of 1 h to 21 days. We observed a progression of kinetically‐controlled textural changes in melt and restite minerals and changes in the liquidus mineralogy in response to factors such as volatile loss. During the course of the experiments, both olivine and orthopyroxene recrystallized at different times. Rare relic chondrules could still be identified after 21 days. The silicate melts that form are very heterogeneous, in terms of both major and trace element chemistry, reflecting heterogeneity of the localized mineral assemblage, particularly with respect to phosphates and clinopyroxene. Metal‐sulfide melts formed in short‐duration runs are also heterogeneous. The experimental data are relevant to aspects of the genesis of primitive achondrites such as the acapulcoites. The observed textures are consistent with a model for acapulcoite petrogenesis in which silicate melting was limited to only a few volume percent of the chondritic source rock. The experiments are also relevant to the behavior of chondritic material that has been partially melted in an impact environment. 相似文献
13.
Paul V. Burger James J. Papike Charles K. Shearer Jim M. Karner 《Geochimica et cosmochimica acta》2009,73(11):3248-318
Growth zoning in jarosite, an Fe3+-bearing sulfate mineral, can generally be characterized by variation of Na+ for K+ in the crystallographic A site or by Al3+ for Fe3+ in the octahedral (B) site. Growth zoning in a sample from Post Pit, NV, however, is more complicated than has been observed in other jarosite samples examined in this study and by previous work, and is characterized by varying Ba, Sr, P, and As. In this sample, these elements define a coupled substitution in which Ba2+ and Sr2+ substitute for K+ in the crystallographic A site, and are balanced by the substitution of P5+ and As5+ for S6+ in the tetrahedral (X) site. The Post Pit sample also exhibits a high concentration of V, which does not appear to participate in the aforementioned coupled substitution. Analysis of mineral stoichiometry and charge balance reveal that V is likely tetravalent, and represents a charge excess in the B site. The occurrence of V-bearing goethite in this sample records fluctuating fluid pH, resulting in the alternating stability of jarosite and goethite. Measurement of the REEs in jarosite by SIMS, indicate that Ce is trivalent in the Post Pit sample; reduced relative to Ce4+ found in the remainder of the sample suite. The presence of V4+ and Ce3+ indicate that the Post Pit sample was deposited in a less oxidizing environment than the remainder of the sample suite. This study illustrates how jarosite crystal chemistry can be used to place relative constraints on fluid conditions (pH, Eh, chemistry, etc.) in the terrestrial environment, and characterizes possible major and trace element coupled substitutions into the jarosite crystal structure. Furthermore, this study provides a framework for future studies to examine mineral-fluid partition coefficients (D values) which may place more absolute constraints on fluid chemistry in the jarosite depositional environment. 相似文献
14.
Joan R. Clark Daniel E. Appleman J. J. Papike 《Contributions to Mineralogy and Petrology》1968,20(1):81-85
Bond distances and angles in isostructural, ordered clinopyroxenes are compared for eight compositions, based on five new and three published crystal-structure refinements from X-ray diffraction data. Unit-cell parameters and configuration of the silicate chains are directly correlated with cation composition and distribution in the M2 and M1 sites.Publication authorized by the Director, U. S. Geological Survey.Our thanks go to D. B. Stewart, C. Milton, and C. S. Ross, U. S. Geological Survey, who supplied crystals of the minerals, to D. B. Stewart for synthesis of iron spodumene, to Dr. L. Fuchs, Argonne National Laboratory, for synthesis of ureyite, and to Dr. B. Mason, U. S. National Museum, who transmitted the ureyite crystals. 相似文献
15.
Peter I. Nabelek Gilbert N. Hanson Theodore C. Labotka James J. Papike 《Contributions to Mineralogy and Petrology》1988,99(1):49-61
In this paper we consider the mechanisms by which the mineralogy and composition of the margins of the Notch Peak granitic stock, Utah, were affected by calcareous argillite country rocks. The contact zone of the granite relative to the unaffected granite is enriched in: K2O from about 4 to 10 wt.%, Rb from 250 to 510 ppm, Sr from 150 to 790 ppm and Ba from 250 to 2160 ppm. Locally, some of the intrusive rocks at the contact are nearly devoid of quartz and can be classified as syenites. The initial 87Sr/86Sr ratios range from 0.7069 in the unaffected rocks to 0.7100 in the potassium-enriched samples, approaching the values of the calc-silicate country rocks of about 0.7110.Calculations show that the characteristics of the contact zone near the top of the stock are the result of a number of sequential processes. CO2-rich fluids derived from the heated calcareous argillites apparently caused a shift in the phase boundaries in the magma, enhancing accumulation of K-feldspar and high-Ca augite at the expense of other phases. The accumulation resulted in the high Ba and Sr concentrations in some samples. However, the high K2O and Rb concentrations and magmatic 18O values indicate infiltration of magmatic fluid emanating from the solidifying lower portions of the pluton subsequent to solidification of the cap. The minimum fluid-rock ratios of 4.6 by mass, calculated on the basis of K2O and Rb concentration shifts, indicate that a substantial amount of the fluid was channeled through this contact zone. The desilication of the rocks forming the syenitic samples at the contact apparently occurred when a chemical potential gradient of silica between the granite and wall-rocks was established as quartz was consumed in the wall-rocks during calc-silicate reactions. The infiltrating magmatic fluid probably acted as a medium for transport of silica across the contact and perhaps exchange of Sr between the country rocks and the intrusion where up to 30% of strontium in the granitic and syenitic samples from the contact zone was derived from the calc-silicates. The syenitic rocks cannot be explained by desilication reactions involving assimilation of the calc-silicates by the granite magma. The results of this study show that fluids interacting with the country rocks need to be considered to explain the effects of country rocks on the composition of the margins of granitic intrusions. 相似文献
16.
Richard J. Walker G. N. Hanson J. J. Papike J. R. O''Neil 《Geochimica et cosmochimica acta》1986,50(12):2833-2846
The Nd, O and Sr isotopic characteristics of Precambrian metasedimentary, metavolcanic and granitic rocks from the Black Hills of South Dakota are examined. Two late-Archean granites (2.5-2.6 Ga) have Tdm ages of 3.05 and 3.30 Ga, suggesting that at least one of the granites was derived through the melting of significantly older crust. Early-Proterozoic metasedimentary rocks have Tdm ages that range from 2.32 to 2.45 Ga. These model ages, in conjunction with probable stratigraphic ages ranging from 1.9 to 2.2 Ga, indicate that mantle-derived material was added to the continental crust of this region during the early-Proterozoic. Previous studies of the Harney Peak Granite complex have reported U-Pb and Rb-Sr ages of about 1.71 Ga and most granite samples examined in this study have Sr isotopic compositions consistent with that age. Two granite samples taken from the same sill, however, give two-point Rb-Sr and Sm-Nd ages of 2.08 ±0.08 and 2.20 ±0.20 Ga (∑2200Nd = −15.5), respectively. In addition, whole-rock and apatite samples of the spatially associated Tin Mountain pegmatite give a Sm-Nd isochron age of 2000 ±100 Ma (∑2200Nd = −5.8 ±1.8).
The Sm-Nd, O and Rb-Sr isotopic systematics of these granitic rocks have been complicated to some degree by both crystallization and post-crystallization processes, and the age of the pegmatite and parts of the Harney Peak Granite complex remain uncertain. Processes that probably complicated the isotopic systematics of these rocks include derivation from heterogeneous source material, assimilation, mixing of REE between granite and country rock during crystallization via a fluid phase and post-crystallization mobility of Sr. The Nd isotopic compositions of the pegmatite and the Harney Peak Granite indicate that they were not derived primarily from the exposed metasedimentary rocks. 相似文献
17.
P. I. Nabelek T. C. Labotka J. R. O'Neil J. J. Papike 《Contributions to Mineralogy and Petrology》1984,86(1):25-34
The Jurassic Notch Peak granitic stock, western Utah, discordantly intrudes Cambrian interbedded pure limestones and calcareous argillites. Contact metamorphosed argillite and limestone samples, collected along traverses away from the intrusion, were analyzed for
18O,
13C, and D. The
13C and
18O values for the limestones remain constant at about 0.5 (PDB) and 20 (SMOW), respectively, with increasing metamorphic grade. The whole rock
18O values of the argillites systematically decrease from 19 to as low as 8.1, and the
13C values of the carbonate fraction from 0.5 to –11.8. The change in
13C values can be explained by Rayleigh decarbonation during calcsilicate reactions, where calculated
is about 4.5 permil for the high-grade samples and less for medium and low-grade samples suggesting a range in temperatures at which most decarbonation occurred. However, the amount of CO2 released was not anough to decrease the whole rock
18O to the values observed in the argillites. The low
18O values close to the intrusion suggest interaction with magmatic water that had a
18O value of 8.5. The extreme lowering of
13C by fractional devolatilization and the lowering of
18O in argillites close to the intrusion indicates oxgen-equivalent fluid/rock ratios in excess of 1.0 and X(CO2)F of the fluid less than 0.2. Mineral assemblages in conjunction with the isotopic data indicate a strong influence of water infiltration on the reaction relations in the argillites and separate fluid and thermal fronts moving thru the argillites. The different stable isotope relations in limestones and argillites attest to the importance of decarbonation in the enhancement of permeability. The flow of fluids was confined to the argillite beds (argillite aquifers) whereas the limestones prevented vertical fluid flow and convective cooling of the stock. 相似文献
18.
A total of seven lithic clasts from the polymict eucrites ALHA76005 and ALHA77302 have been studied petrographically and analyzed with the electron microprobe. All clasts are composed predominantly of pyroxene and plagioclase, ± ilmenite, troilite, Fe-Ni metal, mesostasis, and silica. Pyroxene compositions in unequilibrated clasts and clast bulk compositions, calculated by modal recombination, indicate that the clasts originally crystallized under similar conditions and that they may be genetically related to each other by fractionation of pigeonite and plagioclase. 相似文献
19.
S Swart JJ Zietsman JC Coetzee DG Goslett A Hoek D Needham 《African Journal of Marine Science》2016,38(4):525-538
South Africa’s small-pelagic fishery is a socio-economically important component of the country’s commercial fisheries sector, second in value only to the demersal trawl fishery. Management of this sector relies on infrequent hydro-acoustic surveys, which provide measures of anchovy Engraulis encrasicolus and sardine Sardinops sagax biomass used in the assessments of stock status and in the development of management plans for the sustainable utilisation of these resources. We demonstrate how technological capabilities in ocean robotics at the Council for Scientific and Industrial Research (CSIR) could augment the current resource-intensive hydro-acoustic ship-based survey programme and create opportunities for expanding its spatial and temporal resolution. We successfully implement and demonstrate an autonomous wave glider, fitted with a hydro-acoustic sensor and compare the data to a collocated ‘traditional’ ship-based acoustics survey. In the future these autonomous systems approaches could be seen as a means to lessen the cost burden of the ship-based survey, while at the same time with the added advantage of continuous collection over much wider spatial and temporal domains. This could enable a more reflexive stock management approach taking into account the seasonal characteristics of the fishery and its ecosystem. Gliders thus have potential to increase dramatically the quantity of information available to fisheries managers, thereby reducing uncertainty and contributing to improved management of valuable fish resources. They are likely to contribute to improved knowledge of the ecology of small pelagic fish species off the coast of South Africa in a changing climate and should potentially also permit the collection of biomass data for other marine resources currently not routinely monitored. 相似文献
20.
J.J. Papike 《Geochimica et cosmochimica acta》2009,73(24):7443-19164
Basalts and basaltic cumulates from Mars (delivered to Earth as meteorites) carry a record of the history of that planet - from accretion to initial differentiation and subsequent volcanism, up to recent times. We provide new microprobe data for plagioclase, olivine, and pyroxene from 19 of the martian meteorites that are representative of the six types of martian rocks. We also provide a comprehensive WDS map dataset for each sample studied, collected at a common magnification for easy comparison of composition and texture. The silicate data shows that plagioclase from each of the rock types shares similar trends in Ca-Na-K, and that K2O/Na2O wt% of plagioclase multiplied by the Al content of the bulk rock can be used to determine whether a rock is “enriched” or “depleted” in nature. Olivine data show that meteorite Y 980459 is a primitive melt from the martian mantle as its olivine crystals are in equilibrium with its bulk rock composition; all other olivine-bearing Shergottites have been affected by fractional crystallization. Pyroxene quadrilateral compositions can be used to isolate the type of melt from which the grains crystallized, and minor element concentrations in pyroxene can lend insight into parent melt compositions.In a comparative planetary mineralogy context, plagioclase from Mars is richer in Na than terrestrial and lunar plagioclase. The two most important factors contributing to this are the low activity of Al in martian melts and the resulting delayed nucleation of plagioclase in the crystallizing rock. Olivine from martian rocks shows distinct trends in Ni-Co and Cr systematics compared with olivine from Earth and Moon. The trends are due to several factors including oxygen fugacity, melt compositions and melt structures, properties which show variability among the planets. Finally, Fe-Mn ratios in both olivine and pyroxene can be used as a fingerprint of planetary parentage, where minerals show distinct planetary trends that may have been set at the time of planetary accretion.Although the silicate mineralogical data alone cannot support one specific model of martian magmatism over another, the data does support the basic igneous reservoirs proposed for Mars, and may also be used to constrain some aspects of specific petrogenetic models. Examples include enriched and depleted reservoirs that can be identified by plagioclase K, Na and Al composition, multivalent element partitioning in olivine and pyroxene (V, Cr) elucidates oxygen fugacity conditions of the reservoirs, and minor element concentrations (i.e., Cr in pyx) show that proposed fractional crystallization models linking Y 980459 to QUE 94201 will not work. 相似文献