Chemical evidence for the genesis of the ureilites, the achondrite Chassigny and the nakhlites

Major element and REE, Cr, Sc, V, Ni, Co, Ir, Au, Sr, Ba abundances were determined in three ureilites and the unique achondrite, Chassigny. Chondritic-normalized REE abundance patterns for the ureilites are v-shaped, similar to pallasites, indicating a possible deep-seated origin. The lithophile trace element abundances and v-shaped REE patterns of the ureilites are consistent with a two-stage formation process, the first of which is an extensive partial melting of chondrite-like matter to yield ureilite precursors in the residual solid, which is enriched in Lu relative to La. The second step consists of an admixture of small and variable amounts of material enriched in the light REE. Such contaminating material may be magmas derived from the first formed melt of partial melting of chondrite-like matter.

In contrast to the ureilites, Chassigny has a chondritic-normalized REE pattern which decreases smoothly from La(1.8 × ) to Lu(0.4 × ) and is parallel to and ˜0.25 × the REE pattern in the nakhlitic achondrites. The composition of the magma from which Chassigny crystallized was highly enriched in the light REE; e.g. chondritic normalized La/Lu ˜ 7. The similarity in the fractionated REE patterns (no Eu anomalies) for the olivine-pyroxene Chassigny and for the nakhlites suggests a genetic relationship.

Siderophile trace element relationships in ureilites can be interpreted by three components: (1) ultramafic silicates enriched in Co relative to Ni, (2) an indigenous metal phase remaining after the partial melting event, and (3) a component of the carbon-rich vein material added after the partial melting.     

Derivation of a heterogeneous lithic fragment in the Bovedy L-group chondrite from impact-melted porphyritic chondrules

The Bovedy L-group chondrite contains a light-colored poikilitic lithic fragment with olivine, low-Ca pyroxene and kamacite compositions characteristic of porphyritic chondrules from unequilibrated ordinary chondrites. Its texture, compositional similarities to porphyritic chondrules, and low Na₂O, K₂O and P₂O₅ content indicate that the fragment represents a solidified, slightly fractionated impact melt formed from a source that was rich in porphyritic chondrules. The fragment is heterogeneous, with a progressive increase in the bulk $\text{MgO}\text{FeO}$ ratio and in MgO content of olivines and low-Ca pyroxenes across its length. ${}^{39}\text{Ar}{}^{40}\text{Ar}$ analyses of the fragment and host indicate that the meteorite experienced extensive degassing due to reheating. The approximate age of 0.5–0.94 Byr dates the reheating event and not the formation of the lithic fragment or the Bovedy breccia. This reheating event renders the fragment's and host's metallographic cooling rate of ~ 5 C/Myr (through 500°C) imprecise. However, the absence of martensite and the presence of kamacite. zoned taenite and tetrataenite in the fragment and host are consistent with such slow cooling through 500°C. This cooling rate must have resulted from burial of the fragment-host assemblage beneath insulating material on the Bovedy parent body. If the thermal diffusivity (κ) of this overburden was approximately comparable to that of the lunar regolith (10^?4cm²/sec), then the fragment was buried at a depth ≌ 6.5 km; if K = 10^?2 cm²/sec (similar to chondritic material), then the fragment was buried at a depth ?65 km.     

Genesis of the Angra dos Reis and other achondritic meteorites

Major, minor and trace element abundances were determined in seven Angra dos Reis samples including whole rocks, fassaite (clinopyroxene), olivine and whitlockite separates via sequential instrumental neutron activation analysis. The chondritic normalized rare earth element (REE) abundance pattern for the Angra dos Reis clinopyroxene separates shows a concave downward shape with a small negative Eu anomaly. The strong fractionation between the light and the heavy REE in olivine separates could be attributed to the presence of islands of kirschsteinite in the olivines. The large-ion lithophile trace elements were highly enriched in the whitlockite separate as expected (e.g. La ≈ 370 ppm). The lower Hf and Sc abundances in whitlockite compared to that in the equilibrium “magma” could be the result of favorable partitioning of Hf and Sc in baddeleyite, which may have crystallized prior to or with whitlockite in the interstitial liquid. Comparison of whole rock with mineral separate data shows the presence of ～3% olivine, ～2.6% spinel and small amounts of metallic Ni-Fe and troilite in the whole rock.The trace element abundances in the derivative magma from which the Angra dos Reis clinopyroxene crystallized were estimated from the clinopyroxene data and the clinopyroxene mineral-liquid partition coefficients. From the derivative magma, the trace element abundances in the possible parent magmas were calculated by assuming that these parent magmas have undergone different degrees of clinopyroxene fractional crystallization to yield the Angra dos Reis derivative magma. Using the trace element abundances in these possible parent magmas, a two-stage crystal-liquid fractionation model with source material containing olivine, orthopyroxene and clinopyroxene is presented for the genesis of Angra dos Reis. Possible combinations of the degree of equilibrium non-modal partial melting, the source mineral composition and the initial element abundances required to generate possible Angra dos Reis parent magmas are calculated by the multilinear regression analysis method. Favorable solutions for this two-stage crystal-liquid fractionation model could be that Angra dos Reis crystallized at ～70% fractional crystallization of clinopyroxene from magmas generated by reasonable degrees of equilibrium partial melting (～7–10%) of deep-seated primitive source materials (olivine ～54–30%, orthopyroxene ～33–53%, and clinopyroxene ～13–17%) with trace element (Ba, Sr, REE and Sc) abundances ～3.5–4.7 × chondrites. These calculated REE abundances in the Angra dos Reis parent body are very similar to those suggested for the primordial moon (～3–5 × chondrites).Possible genetic relationships between Angra dos Reis and other achondrites, especially cumulate eucrites and nakhlites, are studied. Apparently, the unique Angra dos Reis could not be related to those achondrites by crystal-liquid fractionation of the same parent body.     

The petrogenesis of L-6 chondrites: insights from the chemistry of minerals

Major, minor and trace element concentrations have been measured in all the volumetrically significant minerals from the L-6 chondrites Alfianello, Colby (WI) and Leedey. Most of the elements show the compositional uniformity observed in other studies. However, REE, Co and Ni are distinctly different in their abundances and their phase distributions in each of the three meteorites. Such differences must manifest differing physical and chemical conditions involved in the formation of each of the three rocks. The distributions of REE and Ni between various phases are compatible with models which assume equilibrium between presently coexisting minerals. Such a model demonstrates how plausible differences in temperature and Ni content of metallic minerals could produce the observed differences in Ni abundances in olivine and clinopyroxene from each of the three chondrites.REE are too abundant in the minerals to have been produced by crystal-liquid fractionation from a magma of whole rock composition.Alkali element abundances are incompatible with a model of closed system equilibration of the meteorites. Rb is underabundant in feldspar relative to Na when compared to the equilibrium model predictions. A portion of the Cs seems to be included in feldspar by diadochic substitution, however, significant amounts are randomly associated with other minerals, perhaps by incorporation into lattice defects and at interstices. Partial loss of this nonfeldspathic Cs may be responsible for the large range of Cs abundances observed in chondrites.     

Empirical estimation of magnetite/liquid distribution coefficients for some transition elements

Magnetite/liquid distribution coefficients have been calculated that are consistent with observed variations in contents of V, Sc, Cr, and Ti in lavas from Craters of the Moon lava field, Idaho. In particular, our average distribution coefficient for V (27±8) is in close agreement with that determined experimentally at the temperature and oxygen fugacity appropriate for crystallization of these lavas. Although this value is not very precise, it shows that V contents of at least some calcalkaline series are consistent with generation of andesitic and related magmas from basaltic parental magmas by crystal fractionation, involving removal of appreciable amounts of magnetite.Current address: Geology Department, Rice University. Houston, Texas 77001, USA     

Assessment of Cyto‐ and Genotoxic Effects of a Variety of Chemicals Using Saccharomyces cerevisiae

Saccharomyces cerevisiae as the most simple eukaryotic organism is broadly accepted as a laboratory model organism. For the detection of potential toxic effects of pure compounds and complex composed samples like wastewater a miniaturised short‐term in vitro cyto‐ and genotoxicity screening assay was developed. The assay based on genetically modified S. cerevisiae cells deleted in the prominent drug efflux transporters Pdr5, Snq2, and Yor1 that facilitate pleiotropic drug resistance. The yeast strain devoid of these proteins that mediate the efflux of structurally diverse hydrophobic compounds exhibited an increased sensitivity to a variety of organic compounds. The DNA damage inducible RAD54 promoter fused to a yeast optimized derivative of the GFP (green fluorescent protein) gene from the jelly fish Aequorea victoria served as an indicator of DNA damage in this strain. Various pure compounds including the direct‐acting genotoxins methyl‐N‐nitro‐N‐nitrosoguanidine (MNNG), 4‐nitroquinoline‐N‐oxide (4‐NQO), methyl methanesulfonate (MMS) and hydroxyurea as well as the heavy metals cadmium and chromium(VI), the insecticide lindane and the central nervous system stimulant caffeine were tested exhibiting dose dependent induction of green fluorescence. All compounds were in parallel examined for chronic toxicity. A bioassay detecting simultaneously geno‐ and cytotoxic effects of potential toxicants in a single assay can be an important tool with a variety of applications in environmental monitoring and aquatic ecotoxicology. By partial automation and miniaturisation to microtitration scale this bioassay enables sensitive and fast biomonitoring for a multitude of samples.     

U–Pb zircon geochronology of silicic tuffs from the Timber Mountain/Oasis Valley caldera complex, Nevada: rapid generation of large volume magmas by shallow-level remelting

Large volumes of silicic magma were produced on a very short timescale in the nested caldera complex of the SW Nevada volcanic field (SWNVF). Voluminous ash flows erupted in two paired events: Topopah Spring (TS, >1,200 km³, 12.8 Ma)–Tiva Canyon (TC, 1,000 km³, 12.7 Ma) and Rainier Mesa (RM, 1,200 km³, 11.6 Ma)–Ammonia Tanks (AT, 900 km³, 11.45 Ma; all cited ages are previously published ⁴⁰Ar/³⁹Ar sanidine ages). Within each pair, eruptions are separated by only 0.1–0.15 My and produced tuffs with contrasting isotopic values. These events represent nearly complete evacuation of sheet-like magma chambers formed in the extensional Basin and Range environment. We present ion microprobe ages from zircons in the zoned ash-flow sheets of TS, TC, RM, and AT in conjunction with δ¹⁸O values of zircons and other phenocrysts, which differ dramatically among subsequently erupted units. Bulk zircons in the low-δ¹⁸O AT cycle were earlier determined to exhibit ∼1.5‰ core-to-rim oxygen isotope zoning; and high-spatial resolution zircon analyses by ion microprobe reveal the presence of older grains that are zoned by 0.5–2.5‰. The following U–Pb isochron ages were calculated after correcting for the initial U–Pb disequilibria: AT (zircon rims: 11.7 ± 0.2 Ma; cores: 12.0 ± 0.1 Ma); pre-AT rhyolite lava: (12.0 ± 0.3 Ma); RM: 12.4 ± 0.3); TC: (13.2 ± 0.15 Ma); TS: (13.5 ± 0.2). Average zircon crystallization ages calculated from weighted regression or cumulative averaging are older than the Ar–Ar stratigraphy, but preserve the comparably short time gaps within each of two major eruption cycles (TS/TC, RM/AT). Notably, every sample yields average zircon ages that are 0.70–0.35 Ma older than the respective Ar–Ar eruption ages. The Th/U ratio of SWNVF zircons are 0.4–4.7, higher than typically found in igneous zircons, which correlates with elevated Th/U of the whole rocks (5–16). High Th/U could be explained if uranium was preferentially removed by hydrothermal solutions or is retained in the protolith during partial melting. For low-δ¹⁸O AT-cycle magmas, rim ages from unpolished zircons overlap within analytical uncertainties with the ⁴⁰Ar/³⁹Ar eruption age compared to core ages that are on average ∼0.2–0.3 My older than even the age of the preceding caldera forming eruption of RM tuff. This age difference, the core-to-rim oxygen isotope zoning in AT zircons, and disequilibrium quartz–zircon and melt-zircon isotopic fractionations suggest that AT magma recycled older zircons derived from the RM and older eruptive cycles. These results suggest that the low-δ¹⁸O AT magmas were generated by melting a hydrothermally-altered protolith from the same nested complex that erupted high-δ¹⁸O magmas of the RM cycle only 0.15 My prior to the eruption of the AT, the largest volume low-δ¹⁸O magma presently known.Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.     

The Stellar Content of Active Galaxies

We present the results of a long-slit spectroscopic study of 38 active and four normal galaxies. Stellar absorption features, continuum colours and their radial variations are analysed in an effort to characterize the stellar population in these galaxies and detect the presence of a featureless continuum underlying the starlight spectral component. Spatial variations of the equivalent widths of conspicuous absorption lines and continuum colours are detected in most galaxies. Star-forming rings, in particular, leave clear fingerprints in the equivalent widths and colour profiles. We find that the stellar populations in the inner regions of active galaxies present a variety of characteristics, and cannot be represented by a single starlight template. Dilution of the stellar lines by an underlying featureless continuum is detected in most broad-lined objects, but little or no dilution is found for most of the 20 type 2 Seyferts in the sample. Colour gradients are also ubiquitous. In particular, all but one of the observed Seyfert 2s are redder at the nucleus than in its immediate vicinity. Possible consequences of these findings are briefly outlined.     

Hydrothermal gases offshore Milos Island, Greece

Hydrothermal fluids emerge from the seafloor of Paleohori Bay on Milos. The gases in these fluids contain mostly CO₂ but CH₄ concentrations up to 2% are present. The stable carbon isotopic composition of the CO₂ (near 0%) indicates an inorganic carbon source (dissociation of underlying marine carbonates). The carbon and hydrogen isotopes of most CH₄ samples are enriched in the heavy species (δ¹³C = −9.4 to −17.8‰; δD = −102 to −189‰) which is believed to be characteristic for an abiogenic production of CH₄ by CO₂-reduction (Fischer-Tropsch reactions). Depletions in the deuterium content of three CH₄ samples (to −377%) are probably caused by unknown subsurface rock alteration processes. Secondary hydrogen isotope exchange processes between methane, hydrogen and water are most likely responsible for calculated unrealistic methane formation temperatures.

We show that excess helium, slightly enriched in ³He, is present in the hydrothermal fluids emerging the seafloor of Paleohori Bay. When the isotopic ratio of the excess component is calculated a ³He/⁴He_excess of 3.6 · 10⁻⁶ is obtained: This indicates that the excess component consists of about one third of mantle helium and two thirds of radiogenic helium. We infer that the mantle-derived component has been strongly diluted by radiogenic helium during the ascent of the fluids to the surface.