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1.
Suspended matter from the surface waters of the Amazon Estuary were collected during May and June 1976 on the ‘R/V Alpha Helix’, and their major-element compositions (Al, Si, Ti, K, Mg, Ca, P, Fe and Mn) were measured.Between salinities of 0 and 10%. the suspended material, predominantly terrigenous in derivation, decreases in load from 500 to 3 mg/l, but has a chemical composition which remains essentially constant. With the onset of a large amount of biological productivity at approximately 10%. salinity, there are large increases in the ratios of , , , , and which are maintained at higher salinities. Calculations of “excess” concentrations of elements held in the non-terrigenous components of the suspended material further support our main conclusion that Si, P, Ca, Mg, Ti and Mn are incorporated into the skeletal and organic phases of marine phytoplankton (predominately diatoms) of the Amazon Estuary. The data suggest, but with less certainty, that Fe and K follow the above elements.This study has demonstrated that the chemical composition of river-introduced suspended matter can be significantly altered by biological activity within estuarine waters as can be the geochemical cycle of inorganic elements. 相似文献
2.
Rapid accumulation of CaCO3 is occurring in Littlefield Lake, a marl lake located in central Michigan. The sediment, which is 95% CaCO3, primarily consists of eight different genetic groups of carbonate allochems. These include calcite muds, sands, algal oncoids and Chara encrustations, as well as the dominant aragonitic gastropods Valvota tricarinota. Gyraulus deflectus and Amnicola integra. and the dominant aragonitic pelecypod Sphaerium partumeium. Samples of each of these groups were analyzed for Ca, Sr and Mg. Molar ratios are primarily controlled by allochem mineralogy, with calcitic forms having ratios 5–10 times larger than aragonitic (shelled) forms. The ratios are primarily controlled by biochemical fractionation, and are significantly lower than ratios of inorganically precipitated aragonite from other settings. Partition coefficients were determined for both Sr and Mg for each carbonate allochem group and, based on comparisons with results reported by other workers, the partition coefficients determined here are generally considered ‘typical’ or representative values for biogeneous freshwater carbonates. An analysis of variance of the data indicates that most genera and species of carbonate-secreting organisms in marl lakes have highly characteristic and ratios. These ratios can potentially serve as geochemical tracers in future investigations of lacustrine carbonate diagenesis. Both Sr and Mg are influenced by grain size and/or surface area, probably due to the presence of these elements in non-lattice-held (exchangeable) positions. 相似文献
3.
The 2.7 Ga Kambalda Sequence comprises a mafic to ultramafic dominated volcanic rock sequence of the Kalgoorlie Terrane, Yilgarn Craton, Western Australia. The Sequence is divided into Lower and Upper Units separated by the Kambalda Komatiite Formation. Five basalt suites of the Lower Unit are tholeiitic where MgO spans 5-10 wt.% MgO, with minor assimilation-fractional crystallization (AFC), whereas six volcanic suites identified in the Upper Unit are tholeiitic to komatiitic-basalts with MgO 24-5 wt.% having generally greater degrees of AFC. Upper suites plot at Al2O3/TiO2 (17-26) close to the primitive mantle ratio of 21, and Pt + Pd (19-31 ppb), whereas the PGE-depleted Lower basalts plot at generally lower Al2O3/TiO2 (<16) and Pt + Pd (<10 ppb). Most suites have an average Pt/Pd ratio of 1.11, despite large variations in MgO contents, broadly consistent with the Pt/Pd ratio in the primitive mantle. On primitive mantle-normalised PGE plots, Upper suites generally display less fractionated patterns of the IPGE (Os, Ir, Ru and Rh) from the PPGE (Pt and Pd) relative to the Lower basalts. Most suites exhibit patterns with positive slopes reflecting relative enrichment of Pd, Pt, Au and Cu relative to Ni and IPGE. In suites of both Units, the concentrations of Ir and Ru fall with decreasing MgO contents, indicating their broadly compatible behaviour during magmatic evolution that involved AFC. Platinum and Pd behave as incompatible elements in the high-MgO suites, whereas Pt and Pd behave compatibly during crystallisation of the Lower basalt magmas, an interpretation consistent with progressively higher Cu/Pt and Cu/Pd ratios at decreasing MgO contents, and with falling Pt/Ti, collectively due to sulphur saturation induced by AFC as recorded in an antivariance of Pd/Ir with Nb/Th, a monitor of AFC.Collectively, the data suggest that several of the Lower Basalt suites crystallised under sulphide-saturated conditions, whereas most of the Upper Basalt Sequences remained sulphur undersaturated during magmatic evolution. Alteration, and fractional crystallisation of silicate and oxide phases, can be ruled out as factors governing PGE distribution in these mafic-ultramafic suites. Instead, the data suggest that discrete PGE-bearing phase (s) fractionated from the magmas. Such phases could be platinum group minerals (PGM; e.g., laurite) and/or alloys, or discrete PGE-rich nuggets or sulphides. 相似文献
4.
Stephen P Smith 《Geochimica et cosmochimica acta》1984,48(5):1033-1041
Gabbro and diorite from the Skaergaard layered igneous intrusion contain noble gases which are mixtures of atmospheric and juvenile components. Atmospheric noble gases predominate in samples that have undergone extensive oxygen isotope exchange with meteoric-hydrothermal water. The source of the atmospheric noble gas component is inferred to be the hydrothermal circulation system. A juvenile component with and containing fission xenon is also present This component predominates in samples showing unaltered magmatic oxygen isotope compositions. Neon of atmospheric isotopic composition is associated with the juvenile radiogenic 40Ar and fission xenon. The source of this second noble gas component may be either the crustal country rock or the upper mantle. If the neon is juvenile primordial neon from a mantle source region, terrestrial primordial is the same as atmospheric to within 4%. However, subduction of atmospheric noble gases into the upper mantle may provide an alternate source of neon and other noble gases in the mantle. 相似文献
5.
Asish R. Basu 《Geochimica et cosmochimica acta》1978,42(6):659-668
New analyses of K, Rb, Sr and Ba contents and the ratios of eight amphiboles, one phlogopite, two diopsides and one host alkalic basalt for an amphibole are reported: The samples are mostly inclusions in alkalic basalts and occur in association with peridotite inclusions. Two of the samples are from alpine-type peridotite bodies — one from the Etang de Lhers massif in the French Pyrenees and the other from the Finero massif in the Ivrea zone in northern Italy. The kaersutites come from the following localities: Hoover Dam, Arizona; Deadman Lake, California; Massif Central, France; Queensland; Spring Mountain, New South Wales.The data indicate that kaersutitic amphiboles are genetically unrelated to their host basalts. The isotopic and trace element data of these amphiboles further strengthens the suggestion of BASU and MURTHY (1977) that kaersutites play a significant role in ocean ridge basalt genesis. In addition, pargasitic amphibole with higher ratios, if present, may be important in the source regions of alkalic basalts.The bulk amphibole lherzolite from Lherz has the ratio and ratio appropriate for source material of ridge tholeiites. If the diopside and the amphibole in this rock had isotopically equilibrated under upper mantle conditions, the data show the time of last equilibration to be approximately 735 m.y., in contrast to the young emplacement age of the ultramafic massif.The coexisting phlogopite and diopside in the spinel lherzolite inclusion from Kilbourne Hole, New Mexico, show, surprisingly, isotopic equilibration under upper mantle conditions despite their drastically different ratios. The data show that the phlogopite must have formed very recently in the upper mantle. This phlogopite also has a high ratio (1133), contrary to the commonly held view that mantle phlogopites have low ratios. The coexisting diopside shows high K content (778 ppm) and a lower ratio than the phlogopite. This phlogopite lherzolite has trace elemental and isotopic characteristics that may be adequate for the origin of alkalic basalts upon partial melting. 相似文献
6.
Nd and Sr isotopic compositions as well as trace element concentrations have been determined on a suite of alkali basalts from the Massif Central, in France. Samples show a typical enrichment in incompatible elements. In particular, the REE patterns exhibit a strong fractionation characterized by a ( ratio of about 20. The YbN content is about 10 times chondrite. The ratios exhibit a range from 0.512775 to 0.512989, values quite comparable to those from oceanic island basalts. The ratios vary between 0.70338 and 0.70458 and are anti-correlated with the Nd isotopic ratio.The isotopic and the trace element (in particular REE) data have been used in order to quantitatively model the genesis of the alkali basalts. Among the several types of models tested here, the most likely one appears to be the model of mantle metasomatism. A semi-quantitative approach shows that the source of alkali basalts from the Massif Central was metasomatized prior to melting. In such a model, the basalts could be produced by rather high degrees of partial melting (such as 10 or 15%) of the metasomatically enriched mantle. 相似文献
7.
We present field, petrographic, major and trace element data for komatiites and komatiite basalts from Sargur Group Nagamangala greenstone belt, western Dharwar craton. Field evidences such as crude pillow structure indicate their eruption in a marine environment whilst spinifex texture reveals their komatiite nature. Petrographic data suggest that the primary mineralogy has been completely altered during post-magmatic processes associated with metamorphism corresponding to greenschist to lower amphibolite facies conditions. The studied komatiites contain serpentine, talc, tremolite, actinolite and chlorite whilst tremolite, actinolite with minor plagioclase in komatiitic basalts. Based on the published Sm-Nd whole rock isochron ages of adjoining Banasandra komatiites (northern extension of Nagamangala belt) and further northwest in Nuggihalli belt and Kalyadi belt we speculate ca. 3.2–3.15 Ga for komatiite eruption in Nagamangala belt. Trace element characteristics particularly HFSE and REE patterns suggest that most of the primary geochemical characteristics are preserved with minor influence of post-magmatic alteration and/or contamination. About 1/3 of studied komatiites show Al-depletion whilst remaining komatiites and komatiite basalts are Al-undepleted. Several samples despite high MgO, (Gd/Yb)N ratios show low CaO/Al2O3 ratios. Such anomalous values could be related to removal of CaO from komatiites during fluid-driven hydrothermal alteration, thus lowering CaO/Al2O3 ratios. The elemental characteristics of Al-depleted komatiites such as higher (Gd/Yb)N (>1.0), CaO/Al2O3 (>1.0), Al2O3/TiO2 (<18) together with lower HREE, Y, Zr and Hf indicate their derivation from deeper upper mantle with minor garnet (majorite?) involvement in residue whereas lower (Gd/Yb)N (<1.0), CaO/Al2O3 (<0.9), higher Al2O3/TiO2 (>18) together with higher HREE, Y, Zr suggest their derivation from shallower upper mantle without garnet involvement in residue. The observed chemical characteristics (CaO/Al2O3, Al2O3/TiO2, MgO, Ni, Cr, Nb, Zr, Y, Hf, and REE) indicate derivation of the komatiite and komatiite basalt magmas from heterogeneous mantle (depleted to primitive mantle) at different depths in hot spot environments possibly with a rising plume. The low content of incompatible elements in studied komatiites suggest existence of depleted mantle during ca. 3.2 Ga which in turn imply an earlier episode of mantle differentiation, greenstone volcanism and continental growth probably during ca. 3.6–3.3 Ga which is substantiated by Nd and Pb isotope data of gneisses and komatiites in western Dharwar craton (WDC). 相似文献
8.
Robin Brett 《Geochimica et cosmochimica acta》1984,48(6):1183-1188
The oxygen fugacity (fO2) of the Earth's upper mantle appears to lie somewhat above that of the iron-wüstite buffer, its fO2 is assumed to have been similar to the present value at the time of core formation. In the upper mantle, the Fe-rich liquid protocore that would form under such conditions of fO2 at elevated temperatures would lie predominantly in the system Fe-S-O. Distribution coefficients for Co, Cu, Ni, Ir, Au, Ir, W, Re, Mo, Ag and Ga between such liquids and basalt are known and minimum values are known for Ge. From these coefficients, upper mantle abundances for the above elements can be calculated by assuming cosmic abundances for the whole Earth and equilibrium between the Fe-S-O protocore and upper mantle. These calculated abundances are surprisingly close to presently known upper mantle abundances; agreements are within a factor of 5, except for Cu, W, and Mo. Therefore, siderophile element abundances in the upper mantle based on known distribution coefficients do not demand a late-stage meteoritic bombardment, and a protocore formed from the upper mantle containing S and O seems likely.As upper mantle abundances fit a local equilibrium model, then either the upper mantle has not been mixed with the rest of the mantle since core formation, or else partition coefficients between protocore and mantle were similar for the whole mantle regardless of , , and fO2. The latter possibility seems unlikely over such a range. 相似文献
9.
The carbon isotopic composition of 66 inclusion-containing diamonds from the Premier kimberlite, South Africa, 93 inclusion-containing diamonds and four diamonds of two diamond-bearing peridotite xenoliths from the Finsch kimberlite, South Africa was measured. The data suggest a relationship between the carbon isotopic composition of the diamonds and the chemical composition of the associated silicates. For both kimberlites similar trends are noted for diamonds containing peridotite-suite inclusions (P-type) and for diamonds containing eclogite-suite inclusions (E-type): Higher δ13C P-type diamonds tend to have inclusions lower in SiO2 (ol), Al2O3 (opx, gt), Cr2O3, MgO, (ol, opx, gt) and higher in FeO (ol, opx, gt) and CaO (gt). Higher δ13C E-type diamonds tend to have inclusions lower in SiO2, Al2O3 (gt, cpx), MgO, (gt), Na2O, K2O, TiO2 (cpx) and higher in CaO, (gt, cpx).Consideration of a number of different models that have been proposed for the genesis of kimberlites, their xenoliths and diamonds shows that they are all consistent with the conclusion that in the mantle, regions exist that are characterized by different mean carbon isotopic compositions. 相似文献
10.
Margaret Lois Delaney Allan W.H.Bé Edward A. Boyle 《Geochimica et cosmochimica acta》1985,49(6):1327-1341
Constant-temperature laboratory culture experiments of the planktonic foraminiferal species Globigerinoides sacculifer (Brady) suggest that the ratios of Li and Sr to Ca in the shells are a function of these ratios in the culture solutions. and in the shells did not vary with changes of these ratios in the culture solution. These are the first direct determinations of the relationship between foraminiferal shell chemistry and solution composition.The possibility of temperature dependence for the minor elemental composition of foraminiferal shells was also investigated in the laboratory and by analysis of several planktonic and one benthic foraminiferal species from sediment trap and sediment core samples. The , , and ratios in the natural samples roughly correlate with calcification temperature, whereas differences in the Li/Ca ratios are small and not systematically related to temperature. However, laboratory culture experiments at 20°C and 30°C showed no variation in the , , , and ratios with calcification temperature for the planktonic foraminifera G. sacculifer and Orbulina universa. Therefore, observed differences in the , , and ratios for the sediment trap and core foraminiferal samples cannot be ascribed to direct effects of calcification temperature, but may be due to some other environmental factor which is correlated with temperature. 相似文献
11.
Alteration of basaltic glass: Mechanisms and significance for the oceanic crust-seawater budget 总被引：1，自引：0，他引：1
Alteration of basaltic glass to palagonite is characterized by a nearly isomolar exchange of SiO2, Al2O3, MnO, MgO, CaO, Na2O, P2O5, Zn, Cu, Ni, Cr, Hf, Sc, Co and REE for H2O and K2O, whilst TiO2 and FeO are passively accumulated during removal of the remaining cations. The network forming cations Al and Si are removed from the glass in proportion to the gain in Ti and Fe, whilst the other cations do not show a significant relationship to the amount of Ti and Fe accumulation. Sr isotopic data show that during palagonite formation approximately 85% of the basaltic Sr is lost to the hydrous solutions and 40% of seawater Sr is added to the glass, yielding an average loss of the same order of magnitude as of the network forming cations. Losses and gains of oxides yield an average increase of +105% TiO2.K, Rb, and Cs show high increases, but and ratios indicate two different alteration processes: (1) formation of palagonite involves a drastic decrease in these ratios, indicating structural similarities between palagonite and smectite; (2) surface alteration of glass is characterized by an increase in and ratios, probably best interpreted as sorption of alkalies in ratios approximating those of seawater.The total fluxes involved in alteration of glass in the upper portion of the oceanic crust are estimated from the modal abundance of palagonite in the oceanic crust and the abundance of the vein materials smectite and carbonate. Smectite and carbonates act as a sink for a significant portion of the elements liberated up during alteration of basaltic glass except for Na and Al, which are probably taken up by zeolites and/or albite, possibly hidden in the macroscopic estimate of carbonate. Formation of the observed quantity of secondary phases requires additional sources for Si, Fe. Ca and K. K is provided in excess from the inflowing seawater at reasonable water/rock ratios. The remaining excess Ca, Si and Fe required may be derived by alteration of interstitial glass and breakdown of anorthite rich plagioclase and titano-magnetite, and/or by supply of deeper seated metamorphic reactions. 相似文献
12.
Concentrations of potassium and rubidium are reported for 62 Precambrian shield whole-rock samples belonging to the pyroxene granulite facies of world-wide distribution. Compared with the Main Trend established by Shaw (1968) for igneous and quasi-igneous rocks of the upper crust, the high-grade metamorphic granulites exhibit a similar correlation but with a measurable depletion in Rb for a given K content. The Metamorphic Trend may be described by the equations: log10 (ppm Rb) = 1.136 log10 (per cent K) + 1.495 or ppm Rb = 31.28 (per cent K)1.136. The square of the product moment correlation coefficient shows that 80 per cent of the variation in Rb is associated with variation in K.All suites studied have initial ratios less than 0.707. This low value argues against repeated extraction of Rb and K through time on a regional scale. Rather, the major depletion in these lithophile elements occurred in the early stages of crustal evolution. 相似文献
13.
Chlorine has a higher solubility in basaltic magmas than other volatiles. A theoretical degassing model predicts that less than 10% of the chlorine originally present in the magma is lost to the atmosphere during surface degassing. This prediction is born out by strong correlation between chlorine and nonvolatile elements in samples from recent volcanic eruptions in Iceland. It is concluded that the chlorine content of subaerial basaltic lavas is proportional to the chlorine content of the magmas. Assuming a roughly constant ratio between chlorine and water in the magmatic gas phase and assuming further that this ratio approximates the ratio in sea water and sediments it is possible to assign each basaltic magma a fixed amount of water. The figures thus obtained (0.3–1.2% H2O) are identical with previously assumed water contents of basaltic magmas.The implied water contents of the melts are discussed in terms of derivation from hydrous mantle phases. It is concluded that such phases can supply only a fraction of the assumed water content, the rest is derived from an additional volatile source in the mantle. The mantle source giving rise to alkali basalts in Iceland has a lower content of volatiles than the tholeiite source. 相似文献
14.
Warwick J. Sivell 《Contributions to Mineralogy and Petrology》1986,93(3):381-394
Extremely fractionated basaltic to ferrobasaltic amphibolites and granulites comprise two spatially associated mafic tholeiitic suites (?deformed sills) within the Early Proterozoic Oonagalabi basement gneiss complex, Harts Range, Central Australia. The metatholeiites are characterised by high to very high FeO, TiO2 and P2O5 contents, and variable depletion in CaO and Al2O3. Despite similar Zr/Nb ratios, the rocks from the two suites show different degrees of enrichment in LREE and other “immobile” incompatible elements. The basaltic melts which were parental to the two mafic suites were not comagmatic and the rocks cannot be related simply by fractionation of realistic assemblages of low-pressure fractionating phases. The data suggest that primary basaltic liquids for the two suites were derived by different degrees of partial melting from essentially similar undepleted mantle source regions. Clinopyroxene in the residual mantle assemblage controlled the composition of the segregating melt at lower degrees of melting. The ferrobasaltic compositions imply long residence times for the basaltic magmas in shallow-level differentiating tholeiitic sills and/or magma chambers in a mature propagating rift environment. High-grade (granulite facies) metamorphism, and subsequent restricted metasomatic reequilibration of the mafic rocks with interlayered migmatitic and quartzofeldspathic gneisses, have affected only abundances of certain highly-smobile elements (e.g. K2O and Rb), resulting in the partial disruption of inter-element correlations. However, the geochemical data do not indicate any large-scale depletion of large ion lithophile elements (LILE) in the Oonagalabi gneiss complex. 相似文献
15.
High precision mass spectrometric determination of calcium isotope ratios allows the 40K → 40Ca radioactive decay to be used for dating a much broader range of geologic materials than is suggested by previous work. is used to monitor enrichments in 40Ca and can be measured to ±0.01% (2σ) using an exponential mass discrimination correction (Russell et al., 1978) and large ion currents. The earth's mantle has such a low (～0.01) that it has retained “primordial” ± 0.011 (normalized to ), as determined by measurements on two meteorites, pyroxene from an ultramafic nodule, metabasalt, and carbonatite. ratios can be conveniently expressed relative to this value as ?Ca in units of 10?4. To test the method for age dating, a mineral isochron has been obtained on a sample of Pikes Peak granite, which has been shown to have concordant KAr, RbSr, and UPb ages. Plagioclase, K-feldspar, biotite, and whole rock yield an age of 1041 ± 32 m.y. (2σ) in agreement with previous age determinations (λK = 0.5543 b.y.?1, , 40K = 0.01167%). The initial of 151.024 ± 0.016 (?Ca = +0.5 ± 1.0), indicates that assimilation of high K/Ca crust was insufficient to affect calcium isotopes. Measurements on two-mica granite from eastern Nevada indicate that the magma sources had K/Ca ≈ 1, similar to intermediate-composition crustal rocks. These results show that the KCa system can be used as a precise geochromometer for common felsic igneous and metamorphic rocks, and may prove applicable to sedimentary rocks containing authigenic K minerals. The relatively short half-life of 40K, the non-volatile daughter, and the fact that potassium and calcium are stoichiometric constituents of many minerals, make the KCa system complementary to other dating methods, and potentially applicable to a variety of geologic problems. 相似文献
16.
Paul H Warren 《Geochimica et cosmochimica acta》1983,47(9):1559-1571
Analysis of the Eu and Sr “anomalies” of eucrites and lunar rocks allows constraints to be placed on the bulk compositions of the eucrite parent body (EPB) and the Moon. The elements Al, REE, and Sr, all are essentially incompatible with the major minerals of these small, low-?(O2) bodies, except for plagioclase, into which Al, Sr, and Eu tend to concentrate. Therefore, the hypothesis that Al, REE, and Sr in the EPB and the Moon are all in proportions close to those in the bulk solar system (i.e., chondrites) leads to certain predictions about the concentrations of these elements in samples affected by plagioclase fractionation. The predictions are almost ideally fulfilled by eucrites and lunar samples. For the EPB, the ratios , , and are constrained to be probably within 10%, almost certainly within 20%, of the chondritic ratios. For the more complicated Moon, the constraints are less precise: is very probably within 25% of chondritic; and are probably within 35% of chondritic. These findings are proof that there is a strong similarity between the bulk compositions of the planets and the compositions of chondritic meteorites.The eucrites' Sm-Eu-Sr systematics are also valuable sources of constraints on the distribution coefficients for Eu and Sr into plagioclase, at low ?(O2). From the slope of data for noncumulate eucrites on a Eu-Sm plot, D(Eu,pl/liq) can be inferred to be 1.1?0.10.2. From the slope on a Sr-Sm plot, D(Sr,pl/liq)) can be inferred to be 1.5 ± 0.3. In the case of D(Eu), this is in excellent agreement with experimental data. In the case of D(Sr), the empirical result is probably more appropriate for eucritic systems than most experimental data, which, due to compositional effects, scatter widely. 相似文献
17.
ratios measured in Quaternary lavas from Java and the Banda arc of Indonesia range from 0.51242 to 0.51280 and exhibit an inverse correlation with . Isotopically, the Indonesian samples resemble Andean rather than island arc lavas. The samples from Java plot either within, or adjacent to the mantle array, towards higher ratios. Samples from the Banda arc and the anomalous calc-alkaline volcano Papandajan are characterized by relatively low and high ratios. These characteristics are consistent with the interpretation that subducted terrigenous material was involved in the genesis of these lavas. Furthermore the Banda arc samples appear to lie on a mixing line between isotopic compositions characteristic of the mantle and upper continental crust. A high-K trachyte from the alkaline volcano Muriah, Java, has isotopic characteristics of the mantle (, ), which implies that the extreme enrichment in large-ion-lithophile elements in its source must have occurred only shortly before its formation. The inferred ratio of the unmodified mantle beneath Java and the Banda arc is lower than that observed in mid-ocean ridge basalt, which may have important implications for a better understanding of the geochemical structure of the mantle. 相似文献
18.
Robert W. Elias Yoshimitsu Hirao Clair C. Patterson 《Geochimica et cosmochimica acta》1982,46(12):2561-2580
Biopurification factors for Ca with respect to Sr, Ba, and natural, uncontaminated Pb were measured for different nutrient-consumer pairs in a remote subalpine ecosystem. The factor for Sr is expressed as: (nutrient ) ÷ (consumer ). Similar expressions were used for and . It was found that Ca was biopurified of Sr 3-fold, of Ba 16-fold, and of Pb 100-fold in going from rock to sedge leaves. In going from sedge leaf to vole, Ca was biopurified of Sr 4-fold, of Ba 8-fold, and of Pb 16-fold. In going from meadow vole to pine marten, Ca was biopurified of Sr 6-fold, of Ba 7-fold, and of Pb 1.1-fold. Similar ranges of values for these factors were obtained for detrital and amphibian food chains. Fluxes of industrial lead entering the ecosystem as precipitation and dry deposition were measured and it was found that 40% of the lead in soil humus and soil moisture, 82% of the lead in sedge leaves, 92% of the lead in vole, and 97% of the lead in marten was industrial. The natural skeletal ratio in carnivores (4 × 10?8) was determined by means of corrections for inputs of industrial lead, food chain relationships, and measured biopurification factors for the ecosystem studied. This represents a 1700-fold reduction of the average ratio in igneous rocks at the earth's surface (6.4 × 10?5) by the compounding of successive Pb biopurification factors in transferring Ca from rock to carnivore. The natural ratio is similar to the value of 6 × 10?8 observed for in the bones of Peruvians who lived 2000 years ago but is 1/900th of the value of about 3.5 × 10?5 for the skeletal ratio found in present day Americans.This study shows experimentally how the ratio in average surface igneous rock (3 × 10?3) has been reduced 800-fold through compounding of successive biopurification steps to provide the skeletal ratio of about 4 × 10?6 observed in humans. It also provides biopurification factors for Sr and Ba among a number of nutrient-consumer pairs which anthropologists can use to delineate degrees of herbivory in diets of hominids within the last 10,000 years. 相似文献
19.
John W. Larimer 《Geochimica et cosmochimica acta》1975,39(3):389-392
The condensation temperatures of refractory silicates and oxides in a gas of cosmic composition are strongly dependent on the ratio. As the ratio increases from 0.4 to 0.9 (solar ~ cosmic ~ 0.6), condensation temperatures of compounds such as A12O3, Ca2Al2SiO7, MgAl2O4, Mg2SiO4 and MgSiO3 decrease by 50–100°. As increases from 0.9 to 1.0, these temperatures drop an additional 300–400°. Other chemical differences result when include: a new suite of high temperature minerals appears (graphite, CaS, Fe3C, SiC and TiN); the reaction CO + 3H2 → CH4 + H2O proceeds to the right at higher temperatures; and iron, whose condensation temperature is unaffected, condenses at higher temperatures than any silicate or oxide. 相似文献
20.
High-pressure melting experiments were performed at ~26 GPa and ~2,200–2,400°C on synthetic peridotite compositions with varying FeO and Al2O3 contents and on a synthetic CI chondrite analogue composition. Peridotite liquids show a crystallisation sequence of ferropericlase (Fp) followed down temperature by Mg-silicate perovskite (MgPv) + Fp, which contrasts a sequence of MgPv followed by MgPv + Fp observed in the chondritic composition. The difference in crystallisation sequence is a consequence of the different bulk Mg/Si ratios. MgPv/melt partition coefficients for major, minor and trace elements were determined by electron microprobe and secondary ion mass spectrometry. Partition coefficients of tri- and tetravalent elements increase with increasing Al concentration in MgPv. A lattice strain model indicates that Al3+ substitutes predominantly onto the Si-site in MgPv, whereas most elements substitute onto the Mg-site, which is consistent with a charge-compensating coupled substitution mechanism. MgPv/melt partition coefficients for Mg (DMg) and Si (DSi) are related to the melt Mg/Si ratio such that DSi becomes lower than DMg at low Mg/Si melt ratios. We use a crystal fractionation model, based on upper mantle refractory lithophile element ratios, to constrain the amount of MgPv and Ca-silicate perovskite (CaPv) that could have fractionated during a Hadean magma ocean event and could still be present as a chemically distinct heterogeneity in the lower mantle today. We show that a fractionated crystal pile composed of 96% MgPv and 4% CaPv could comprise up to 13 wt% of the entire mantle. 相似文献