The lunar geochemistry of chromium and vanadium     

Stefan Seifert  A. .E. Ringwood 《Earth, Moon, and Planets》1988,40(1):45-70

Crystal/liquid partition coefficients for Cr, V, Mn, and Fe have been determined experimentally between olivine, orthopyroxene, clinopyroxene and silicate melt possesing the composition of a primitive lunar green glass, at oxygen fugacities appropriate to the lunar interior. These species all behave essentially as compatible elements and possess crystal/liquid partition coefficients mostly between 0.3 and 0.9. Partition coefficients for Cr, V, and Mn are generally similar to those of Fe. This implies that crystal/liquid fractionation processes in the lunar interior which do not involve the participation of spinels would not have been effective in fractionating MnO, CrO, and VO from FeO. The well-known constancy of FeO/MnO ratios in nearly all lunar rocks is a reflection of this behaviour. It is shown that comparably strong correlations between CrO-;FeO and VO-;FeO exist for lunar highland breccias and soils from all sites and that these correlations extend to primitive lunar volcanic glasses associated with mare volcanism, strongly suggesting that the CrO/FeO and VO/FeO ratios so derived are of global importance. The observed ratios characterizing differentiated regions of the Moon can be combined with the corresponding ratios for residual refractory portions of the Moon, using measured partition coefficients for Fe, Mg, Cr, V, and Mn between olivine, orthopyroxene and liquid. Bulk Moon abundances for Cr and V have been calculated for a range of reasonable assumptions concerning the petrogenetic relationships between differentiated portions of the Moon and complementary refractory residua consisting of olivine and orthopyroxene mineralogies. Because of the small differences in crystal liquid partition coefficients between FeO, CrO, and VO, these estimates are insensitive to large variations in the models. The bulk Moon is accordingly estimated to contain 2190–2463 ppm Cr and 79–95 ppm V. These values are very similar to the Cr and V contents of the Earth's mantle, estimated as 3010 ppm Cr and 81 ppm V by Sun (1982). The geochemical implications of these similarities are discussed.  相似文献   

Seasonal variation in lysosomal destabilization in oysters,Crassostrea virginica     

Ringwood AH  Hoguet J  Keppler CJ 《Marine environmental research》2002,54(3-5):793-797

Lysosomal destabilization assays have been used as valuable biomarkers of pollutant exposures in a variety of bivalve and fish species. The responses of oysters, Crassostrea virginica, deployed at and native to various reference and degraded sites were evaluated for lysosomal destabilization during both summer and winter seasons. In both native and deployed oysters, lysosomal destabilization rates tended to be higher during the winter at both reference and polluted sites. There are at least two hypothetical explanations. Greater lysosomal destabilization rates may be related to physiological changes associated with mobilization of nutrient reserves during the winter and gametogenesis. However, lysosomal destabilization in deployed oysters was correlated with tissue metal concentrations. These data also support a second hypothesis that seasonal differences in physico-chemical factors (such as reduced levels of acid volatile sulfides) may increase the bioavailability of metals during the winter so that adverse effects are more pronounced.  相似文献   

Expression of P-glycoprotein in southeastern oysters, Crassostrea virginica     

Keppler CJ  Ringwood AH 《Marine environmental research》2001,52(1):81-96

These studies provide important fundamental information regarding the expression of P-glycoprotein (p-gp) in southeastern oysters (Crassostrea virginica). Using rhodamine transport studies, p-gp activity was detected in newly fertilized embryos. A monoclonal antibody (C219) was used to evaluate p-gp expression in oyster tissues. On the basis of laboratory studies, p-gp expression tended to be higher in gill tissues than mantle tissues, and was generally not related to salinity differences. Seasonal studies were conducted with oysters collected monthly for 1 year from Lighthouse Creek, an unpolluted site. There was a general pattern of higher p-gp expression in the warmer months and lower expression in the colder months. In contrast, total gill protein concentrations decreased during the warmer months and increased during the colder months. These studies indicate that there are seasonal patterns in p-gp expression which may represent an adaptive response to natural stressors associated with summer conditions.  相似文献   

Basaltic magmatism and the bulk composition of the moon     

A. E. Ringwood  S. E. Kesson 《Earth, Moon, and Planets》1977,16(4):389-423

The lunar interior is comprised of two major petrological provinces: (1) an outer zone several hundred km thick which experienced partial melting and crystallization differentiation 4.4–4.6 b.y. ago to form the lunar crust together with an underlying complementary zone of ultramafic cumulates and residua, and (2) the primordial deep interior which was the source region for mare basalts (3.2–3.8 b.y.) and had previously been contaminated to varying degrees with highly fractionated material derived from the 4.4–4.6 b.y. differentiation event. In both major petrologic provinces, basaltic magmas have been produced by partial melting. The chemical characteristics and high-pressure phase relationships of these magmas can be used to constrain the bulk compositions of their respective source regions.Primitive low-Ti mare basalts (e.g., 12009, 12002, 15555 and Green Glass) possessing high normative olivine and high Mg and Cr contents, provide the most direct evidence upon the composition of the primordial deep lunar interior. This composition, as estimated on the basis of high pressure equilibria displayed by the above basalts, combined with other geochemical criteria, is found to consist of orthopyroxene + clinopyroxene + olivine with total pyroxenes > olivine, 100 MgO/(MgO + FeO) = 75–80, about 4% of CaO and Al₂O₃ and 2× chondritic abundances of REE, U and Th. This composition is similar to that of the earth's mantle except for a higher pyroxene/olivine ratio and lower 100 MgO/(MgO + FeO).The lunar crust is believed to have formed by plagioclase elutriation within a vast ocean of parental basaltic magma. The composition of the latter is found experimentally by removing liquidus plagioclase from the observed mean upper crust (gabbroic anorthosite) composition, until the resulting composition becomes multiply saturated with plagioclase and a ferromagnesian phase (olivine). This parental basaltic composition is almost identical with terrestrial oceanic tholeiites, except for partial depletion in the two most volatile components, Na₂ and SiO₂. Similarity between these two most abundant classes of lunar and terrestrial basaltic magmas strongly implies corresponding similarities between their source regions. The bulk composition of the outer 400 km of the Moon as constrained by the 4.6-4.4 b.y. parental basaltic magma is found to be peridotitic, with olivine > pyroxene, 100 MgO/ (MgO + FeO) 86, and about 2× chondritic abundances of Ca, Al and REE. The Moon thus appears to have a zoned structure, with the deep interior (below 400 km) possessing somewhat higher contents of FeO and SiO₂ than the outer 400 km. This zoned model, derived exclusively on petrological grounds, provides a quantitative explanation of the Moon's mean density, moment of inertia and seismic velocity profile.The bulk composition of the entire Moon, thus obtained, is very similar to the pyrolite model composition for the Earth's mantle, except that the Moon is depleted in Na (and other volatile elements) and somewhat enriched in iron. The similarity in major element composition extends also to the abundances of REE, U and Th. These compositional similarities, combined with the identity in oxygen isotope ratios between the Moon and the Earth's mantle, are strongly suggestive of a common genetic relationship.  相似文献   

Earth and Venus: A comparative study     

A.E. Ringwood  Don L. Anderson 《Icarus》1977,30(2):243-253

The observed density of Venus is about 2% smaller than would be expected if Venus were a twin planet of the Earth, possessing an identical internal composition and structure. In principle, this could be explained by a process of physical segregation of metal particles from silicate particles in the solar nebula prior to accretion, so that Venus accreted from relatively metal-depleted material. However, this model encounters severe difficulties in explaining the nature of the physical segregation process and also the detailed chemical composition of the Earth's mantle. Two alternative hypotheses are examined, both of which attempt to explain the density difference in terms of chemical fractionation processes. Both of these hypotheses assume that the relative abundances of the major elements Fe, Si, Mg, Al, and Ca are similar in both planets. According to the first hypothesis, a larger proportion of the total iron in Venus is present as iron oxide in the mantle, so that the core-to-mantle ratio is smaller than in the Earth. This model implies that Venus is more oxidized than the Earth, with its lower intrinsic density (i.e., corrected to equivalent pressures and temperatures) due to the larger amount of oxygen present. The difference between oxidation states is attributed to differing degrees of accretional heating arising from the relatively smaller mass of Venus. On the other hand, the second hypothesis maintains that Venus is more reduced than the Earth, with its mantle essentially devoid of oxidized iron. The difference intrinsic densities is attributed to the Earth accreting at a lower temperature than Venus as a result of the Earth's greater distance from the center of the nebula. As a result, large amounts of sulfur accreted on the Earth but not on Venus. The sulfur, which entered the core, is believed to have increased the mean density of the Earth because of its relatively high atomic weight. The hypothesis also implies that most of the Earth's potassium, because of its chalcophile properties, entered the core.These hypotheses are evaluated in the light of existing data. The second hypothesis leads to an intrinsic density for Venus which is only 0.4% smaller than that of the Earth. This difference is much smaller than is believed to exist. A wide range of chemical evidence is found to be unfavorable to this second hypothesis, but to be consistent with the interpretation that Venus is more oxidized than the Earth, as required by the first hypothesis.  相似文献   

Water quality variation and clam growth: Is pH really a non-issue in estuaries?     

Amy H. Ringwood  Charles J. Keppler 《Estuaries and Coasts》2002,25(5):901-907

A tandem deployment system was used to critically evaluate relationships between important water chemistry parameters (pH, salinity, dissolved oxygen) and biotic performance based on clam growth. The effects of environmental conditions on growth of juvenile clams,Mercenaria mercenaria, were determined after 7-day field deployments in cages at reference sites from 1998 to 2000. Continuous measurements of the overlying water chemistry parameters were monitored by deploying an in situ water quality instrument (Hydrolab Datasonde) at the same time. While salinity was identified as an important determinant of clam growth over wide salinity ranges (10–35‰), pH was also found to be a very important parameter, especially in low-salinity regimes (<25‰). Average pH measurements ranged from 7.2 to 7.8; minimal pHs ranged from 6.9 to 7.6. The results indicated that when average pH levels fell below 7.5 or minimum pH levels fell below 7.2, growth rates were <50% that of clams deployed under higher pH conditions. Estuarine systems are generally perceived as being well-buffered so pH is frequently assumed to be unimportant, but our results suggest that pH levels can decline in estuarine systems to levels that can adversely affect biological responses. The potential impacts on biological resources of even moderate decreases in pH, particularly in systems that naturally tend to have lower pH conditions, may be more important than previously realized.  相似文献   

The system Fe-FeO revisited     

A. E. Ringwood  W. Hibberson 《Physics and Chemistry of Minerals》1990,17(4):313-319

The results of a reconnaissance investigation of melting relationships in the system Fe-FeO at 16 GPa were recently described by Kato and Ringwood (1989). The principal sources of uncertainties in those experiments were caused by loss of FeO to sample capsules during runs and the estimation of sample temperatures by an indirect method, based upon a prior calibration of the relationship between power input and temperature. A further set of 24 runs at 16 GPa has been carried out using improved experimental techniques. The melting temperatures of iron and wüstite at 16 GPa are found to be 1945±20° C and 1875±25° C respectively. (Quoted errors do not include possible effects of pressure on thermocouple emf). The Fe-FeO eutectic is now located at 10±2 wt% FeO and 1670±20° C (previously 15.5±3 wt% FeO and 1700±25° C). The new determination of the depression of the melting point of iron by solution of FeO is 27.5° C/wt% FeO as compared to the previous value of 23° C/wt% FeO. The present results show that the contraction of the liquid immiscibility field in the system at high pressure is somewhat larger than was estimated previously. This study confirms the general topology of high pressure phase relationships in the Fe-FeO system obtained by Kato and Ringwood (1989) and has similar implications for the process of core formation within the Earth.  相似文献   

Melting relationships in the system Fe-Feo at high pressures: Implications for the composition and formation of the earth's core     

Takumi Kato  A. E. Ringwood 《Physics and Chemistry of Minerals》1989,16(6):524-538

A reconnaissance investigation has been carried out on melting relationships in the system Fe-FeO at pressures up to 25 GPa and temperatures up to 2200° C using an MA-8 apparatus. Limited studies were also made of the Co-CoO and Ni-NiO systems. In the system FeFeO, the rapid exsolution of FeO from liquids during quenching causes some difficulties in interpretation of textures and phase relationships. The Co-CoO and Ni-NiO systems are more tractable experimentally and provide useful analogues to the Fe-FeO system. It was found that the broad field of liquid immiscibility present at ambient pressure in the Co-CoO system had disappeared at 18 GPa, 2200° C and that the system displayed complete miscibility between molten Co and CoO, analogous to the behaviour of the Ni-NiO system at ambient pressure. The phase diagram of the system Fe-FeO at 16 GPa and from 1600–2200° C was constructed from interpretations based on the textures of quenched run products. The solubility of FeO in molten iron is considerably enhanced by high pressures. At 16 GPa, the Fe-FeO eutectic contains about 10–15 mol percent FeO and the eutectic temperature in this iron-rich region of the system occurs at 1700±25° C, some 350° C below the melting point of pure iron at the same pressure. The solubility of FeO in molten Fe increases rapidly as temperature increases from 1700 to 2200° C. A relatively small liquid immiscibility field is present above 1900° C but is believed to be eliminated above 2200° C. This inference is supported by thermodynamic calculations on the positions of key phase boundaries. A single run carried out on an Fe₅₀ FeO₅₀ composition at 25 GPa and 2200° C demonstrated extensive and probably complete miscibility between Fe and FeO liquids under these conditions. The melting point of iron is decreased considerably by solution of FeO at high pressures; moreover, the melting point gradient (dP/dT) of the Fe-FeO eutectic is much smaller than that of pure iron and is also smaller than that of mantle pyrolite under the P, T conditions studied. These characteristics make it possible for melting of metal phase and segregation of the core to proceed within the Earth under conditions where most of the mantle remains below solidus temperatures. Under these conditions, the core would inevitably contain a large proportion of dissolved FeO. It is concluded therefore, that oxygen is likely to be the principal light element in the core. The inner core may not be composed of pure iron, as often proposed. Instead, it may consist of a crystalline oxide solid solution (Ni, Fe)₂O.  相似文献   

Composition of the core,I. Solubility of oxygen in molten iron at high temperatures     

E. Ohtani  A.E. Ringwood 《Earth and Planetary Science Letters》1984,71(1):85-93

Experiments on the solubility of FeO in molten iron have been carried out at temperatures between 2100 and 2550°C. The results show that liquid FeO is extensively soluble in molten iron at 2500°C and indicate that they probably become completely miscible above 2800°C. Liquid iron in equilibrium with crystalline magnesiowüstite (Mg_0.8Fe_0.2)O which is believed to be an important mineral in the lower mantle, would dissolve about 14 mol.% of FeO at 2500°C and 40 mol.% of FeO at 2800°C. The geochemical implications of these results are discussed. It is concluded that the outer core probably contains a large amount of dissolved FeO and that oxygen is probably the principal light element in the outer core.  相似文献   

A komatiite component in Apollo 16 highland breccias: implications for the nickel-cobalt systematics and bulk composition of the moon     

A.E. Ringwood  Stefan Seifert  Heinrich Wnke 《Earth and Planetary Science Letters》1987,81(2-3)

The lunar crust at the Apollo 16 landing site contains substantial amounts of a “primitive component” in which the ferromagnesian group of elements is concentrated. The composition of this component can be retrieved via an analysis of mixing relationships displayed by lunar breccias. It is found to be a komatiite which is compositionally similar to terrestrial komatiites both in major and minor elements. The komatiite component of the lunar crust is believed to have formed by extensive degrees of melting of the lunar interior at depths greater than were involved in the formation of the lunar magma ocean which was parental to the crust. After formation of the anorthositic crust, it was invaded by extensive flows and intrusions of komatiite magma from these deeper source regions. The komatiites became intimately mixed with the anorthosite by intensive meteoroid impacts about 4.5 b.y. ago, thereby accounting for the observed mixing relationships displayed by the crust. The compositional similarity between lunar and terrestrial komatiites strongly implies a corresponding similarity between the compositions of their source regions in the lunar interior and the Earth's upper mantle. The composition of the lunar interior can be modelled more specifically by combining the komatiite composition with its liquidus olivine composition (as determined experimentally) in proportions chosen so as to produce a cosmochemically acceptable range of Mg/Si ratios for the bulk Moon. Except for higher FeO and lower Na₂O, the range of compositions thereby obtained for the bulk moon is very similar to the composition of the Earth's upper mantle.The effects of meteoritic contamination on the abundances of cobalt and nickel in lunar highland breccias were subtracted on the assumption that the contaminating projectiles were chondritic. The cobalt and nickel residuals thereby obtained were found to correlate strongly with the (Mg + Fe) content of the breccias, demonstrating that the Co and Ni are associated with the ferromagnesian component of the breccias and are genuinely indigenous to the Moon. The lunar highland Co and Ni residuals also display striking Ni/Co versus Ni correlations which follow a similar trend to those displayed by terrestrial basalts, picrites and komatiites. The lunar trends provide further decisive evidence of the indigenous nature of the Co and Ni residuals and suggest the operation of extensive fractionation controlled by olivine-liquid equilibria in producing the primitive component of the lunar breccias. Indigenous nickel abundances at the Apollo 14, 15 and 17 sites are much lower than at the Apollo 16 site, although rocks from all sites follow the same Ni/Co versus Ni trends. It is suggested that the primitive component at the Apollo 14, 15 and 17 sites was generally of basaltic composition, in contrast to the komatiitic nature of the Apollo 16 primitive component.  相似文献