Reevaluation of the lake-sediment chronology in the Dead Sea basin, Israel, based on new Th/U dates     

Aaron Kaufman  Yoseph Yechieli  Michael Gardosh 《Quaternary Research》1992,38(3)

The Dead Sea is surrounded by chemical and detrital sediments that were deposited in its larger precursor lakes, Lake Samra and Lake Lisan. The sedimentary history of these lakes was recon-structed by means of ²³⁰Th/²³⁴U ages of 30 samples, mostly of argonite laminae, from 8 columnar sections up to 110 km apart. The general validity of the ages was demonstrated by subjecting them to tests of internal isotopic consistency, agreement with stratigraphic order, and concordance with ¹⁴C ages. In the south, only the part of the Samra Formation older than 170,000 yr is exposed, while the aragonite-detritus rhythmites found in the central and northern region are generally younger than 120,000 yr. The Lisan Formation started accumulating about 63,000 yr B.P., with the clay and aragonite beds in the south-central area reflecting a rise in water level to at least −280 m. The upper part of the Lisan Formation, the aragonite-rich White Cliff Member, started accumulating about 36,000 yr B.P. The lake probably reached its highest level sometime after this, based on the ages of Lisan sediments preserved in the southernmost reaches of the basin.  相似文献   

Internally consistent gahnitic spinel-cordierite-garnet equilibria in the FMASHZn system: geothermobarometry and applications   总被引：8，自引：0，他引：8  

Geoffrey T. Nichols  Ron F. Berry  David H. Green 《Contributions to Mineralogy and Petrology》1992,111(3):362-377

The equilibrium (Mg, Fe, Zn)₃Al₂Si₃O₁₂+2Al₂SiO₅=3(Mg, Fe, Zn)Al₂O₄+5SiO₂ garnet + sillimanite/kyanitc = spinel + quartz was calibrated in the piston-cylinder apparatus between 11 and 30 kbar, and over the temperature range of 950 to 1200°C. Three experimental mixes of Mg no. [100^*MgO/(MgO+FeO)] 40, 47 and 60, in the FeO –MgO–Al₂O₃–SiO₂–ZnO (FMASZn) system were used under low oxygen fugacities and anhydrous conditions. We derive a ternary Fe–Mg–Zn symmetric mixing model for aluminous spinels in equilibrium with garnet, to quantify the increase in gahnitic end-member of spinel with increasing pressure and descreasing temperature. Further experiments in the spinel-cordieritequartz-sillimanite field were combined with garnet-cordierite data from the literature to produce a consistent set of equations describing the exchange reactions in FMASHZn relevant to quartz-sillimanite bearing rocks at granulite facies conditions. As spinel is an important mineral participating in many rocks of aluminous composition at granulite-facies conditions, and as zinc contributes to an enlargement of spinel's stability field towards higher pressures and lower temperatures, the thermobarometric calibrations presented here will be most significant in delineating the prograde and retrograde trajectory of P-T paths.  相似文献   

Possible role of amphibole in the origin of andesite: some experimental and natural evidence   总被引：1，自引：1，他引：1  

J. D. Foden  D. H. Green 《Contributions to Mineralogy and Petrology》1992,109(4):479-493

Experiments in the system high-A1 basalt (HAB)-water have been conducted in the melting range at pressures between 1 atm. and 10 kbar, defining the amphibole stability field and the composition of liquids which coexist with this amphibole. Plagioclase is the anhydrous liquidus phase between 1 atm. and 10 kbar but in the hydrous runs this role is taken by olivine at <7 kbar and then by clinopyroxene at higher pressures. Because amphibole is never on the high-A1 basalt liquidus it is not likely that andesite is derived from primary basalt by pure fractional crystallisation, although as we discuss, other mechanisms including equilibrium crystallisation might implicate amphibole. If primary basaltic magma undergoes closed-system equilibrium crystallisation, then the amphibole field will be intersected at between 50 and 100°C below the liquidus. The compositions of melts coexisting with amphibole alone do not match those of any of the natural andesite or dacitic lavas associated with the particular high-A1 basalt investigated. Like natural andesites, they become rapidly silica enriched, but they also become far more depleted in TiO₂ and MgO. However, the compositions of liquids lying directly on the divariant amphibole-out reaction zone, where amphibole +liquid coexist with clinopyroxene or olivine (±plagioclase), do resemble those of naturally occurring low-silica andesites. With increasing temperature pargasitic amphibole breaks down via incongruent melting reactions over a narrow temperature range to form a large volume of relatively low-silica basaltic andesite liquid and a crystalline assemblage dominated by either clinopyroxene or olivine. Our important conclusion is that basaltic andesite liquid will be the product of reaction between cooling, hydrous mafic liquid and anhydrous ferromagnesian phases. The solid reactants could represent earlier cumulates from the same or different magma batches, or they could be peridotite wall-rock material. Because the amphibole-out boundary coexisting with liquid is one of reaction, it will not be traversed so long as the phases on the high temperature side remain. Thus, the assemblage amphibole+clinopyroxene±olivine±plagioclase+liquid is one in which the liquid is buffered (within limits), and results reported here indicate that this buffering generates melts of low-silica andesite composition. When tapped to lower pressures these liquids will rise, eventually to fractionate plagioclase-rich assemblages yielding silicarich andesite and dacite melts. Conversely, the partial melting of hornblende pyroxenite, hornblende peridotite or hornblende gabbro can also yield basaltic andesite liquids. The phase relationships suggested by these experiments are discussed in the light of naturally occurring phenocryst and xenolith assemblages from the east Sunda Arc. Primary magmatic additions to the lithosphere of volcanic arcs are basaltic and voluminous upper crustal andesite in these terranes, complemented by mafic and ultramafic crystalline deposits emplaced in the lower crust or close to the Moho. Together these components constitute total arc growth with a basaltic composition and represent the net accreted contribution to continental growth.  相似文献   

Lithic fragments,glasses and chondrules from Luna 16 fines     

Klaus Keil  Gero KuratMartin Prinz  Jonathan A. Green 《Earth and Planetary Science Letters》1972

Bulk compositions of igneous and microbreccia lithic fragments, glasses, and chondrules from Luna 16 fines as well as compositions of minerals in basaltic lithic fragments were determined with the electron microprobe. Igneous lithic fragments and glasses are divided into two groups, the anorthositic-noritic-troctolitic (hereafter referred to as ANT) and basaltic groups. Chondrules are always of ANT composition and microbreccia lithic fragments are divided into groups 1 and 2. The conclusions reached may be summarized as follows: (1) Luna 16 fines are more similar in composition to Apollo 11 than to Apollo 12 and 14 materials (e.g. Apollo 11 igneous lithic fragments and glasses fall into similar ANT and basaltic groups; abundant norites in Luna 16 and Apollo 11 are not KREEP as in Apollo 12 and 14; Luna 16 basaltic lithic fragments may represent high-K and low-K suites as is the case for Apollo 11; rare colorless to greenish, FeO-rich and TiO₂-poor glasses were found in both Apollo 11 and Luna 16; Luna 16 spinels are similar to Apollo 11 spinels but unlike those from Apollo 12). (2) No difference was noted in the composition of lithic fragments, glasses and chondrules from Luna 16 core tube layers A and D. (3) Microbreccia lithic fragments of group 1 originated locally by mixing of high proportions of basaltic with small proportions of ANT materials. (4) Glasses are the compositional analogs to the lithic fragments and not to the microbreccias; most glasses were produced directly from igneous rocks. (5) Glasses show partial loss of Na and K due to vaporization in the vitrification process. (6) Luna 16 chondrules have ANT but not basaltic composition. It is suggested that either liquid droplets of ANT composition are more apt to nucleate from the supercooled state; or basaltic droplets have largely been formed in small and ANT droplets in large impact events (in the latter case, probability for homogeneous and inhomogeneous nucleation is larger. (7) No evidence for ferric iron and water-bearing minerals was found. (8) Occurrence of a great variety of igneous rocks in Luna 16 samples (anorthosite, noritic anorthosite, anorthositic norite, olivine norite, troctolite, and basalt) confirm our earlier conclusion that large-scale melting or partial melting to considerable depth and extensive igneous differentiation must have occurred on the moon.  相似文献   

A synthetic model for daily streamflow     

N. M. D. Green 《Journal of Hydrology》1973,20(4):351-364

This paper presents a model for synthesising daily average streamflow data that is suitable for most rivers in Great Britain. The method is based on a linear interpolation of the logorithms of 5-day average flows. The 5-day average flows are produced using N.T. Kottegoda's statistical model (Thesis, Univ. of Birmingham, 1970). The 5-day model preserves the long-term statistical characteristics of the daily data, while the short-term characteristics such as hydrograph shape are imposed by the interpolation method.

A stochastic error term is superimposed on the interpolated daily flows. This term represents the non-deterministic component of the daily time series. The analysis of the observed error terms represents an important part of this paper.

The riverflow in the Severn at Bewdley is used to demonstrate both the analysis of actual data and the generation of synthetic data. The technique is then applied to data from two other rivers with widely differing characteristics to demonstrate the range of the method.  相似文献   

Contrasted melting relations in a pyrolite upper mantle under mid-oceanic ridge,stable crust and island arc environments     

D.H. Green 《Tectonophysics》1973,17(3):285-297

The pyrolite model composition provides a satisfactory source composition for mantle-derived magmas insofar as major elements and “compatible” trace elements are concerned but there is evidence for mantle inhomogeneity in the abundances of “incompatible” minor and trace elements (e.g., K, Ti, P, Rb, Sr, light rare earth elements etc.). The composition of a magma, assuming a constant source composition, varies according to the pressure, temperature and water pressure or water content of the source region. The latter two variables essentially determine the degree of partial melting of the source region and in considering the chemical composition of the melt and nature of the residual phases, this parameter is of prime importance.For high degrees (> 20% approx.) of partial melting of a pyrolite source region, magmas are of tholeiitic character but are of increasingly undersaturated and alkaline type for lower degrees of partial melting and high pressures. For any chosen degree of melting and fixed water content of the source region, magmas are more olivine-rich at higher pressures. For any chosen pressure and chosen degree of partial melting, magmas are less olivine-rich at high water contents (and thus lower temperatures). Quartz tholeiite magmas may be derived by ~ 30% melting of pyrolite under water-saturated conditions at pressures up to between 17 kbar and 20 kbar. These generalizations may be applied to understand the characteristic magmatism of mid-oceanic ridges, island chains, oceanic islands and orogenic regions.  相似文献   

Experimental study of the stability of cordierite and garnet in pelitic compositions at high pressures and temperatures     

Dr. B. J. Hensen  D. H. Green 《Contributions to Mineralogy and Petrology》1973,38(2):151-166

In pelitic rocks, under conditions of low f _{O 2} and low f _{H 2 O}, the stability of the mineral pair cordierite-garnet is limited by five univariant reactions. In sequence from high pressure and low temperature to high temperature and low pressure these are: cordierite+garnet hypersthene+sillimanite+quartz, cordierite+garnet hypersthene+sapphirine+quartz, cordierite+garnet hypersthene+spinel+quartz and cordierite+garnet olivine+spinel +quartz. In this sequence of reactions the Mg/Mg+Fe²⁺ ratio of all ferro-magnesian minerals involved decreases continuously from the first reaction to the fifth. The five univariant boundaries delimit a wide P-T range over which cordierite and garnet may coexist.Two divariant equilibria in which the Mg/Mg+ Fe²⁺ ratio of the coexisting phases are uniquely determined by pressure and temperature have been studied in detail. P-T-X grids for the reactions cordierite garnet+sillimanite+quartz and cordierite+hypersthene garnet+quartz are used to obtain pressure-temperature estimates for several high grade metamorphic areas. The results suggest temperatures of formation of 700–850° C and load pressures of 5–10 kb. In rare occasions temperatures of 950–1000° C appear to have been reached during granulite metamorphism.On the basis of melting experiments in pelitic compositions it is suggested that Ca-poor garnet xenocrysts found in calc-alkaline magmas derive from admixed pelitic rocks and did not equilibrate with the calc-alkaline magma.  相似文献   

The genesis of basaltic magmas   总被引：29，自引：2，他引：29  

D. H. Green  A. E. Ringwood 《Contributions to Mineralogy and Petrology》1967,15(2):103-190

This paper reports the results of a detailed experimental investigation of fractionation of natural basaltic compositions under conditions of high pressure and high temperature. A single stage, piston-cylinder apparatus has been used in the pressure range up to 27 kb and at temperatures up to 1500° C to study the melting behaviour of several basaltic compositions. The compositions chosen are olivine-rich (20% or more normative olivine) and include olivine tholeiite (12% normative hypersthene), olivine basalt (1% normative hypersthene) alkali olivine basalt (2% normative nepheline) and picrite (3% normative hypersthene). The liquidus phases of the olivine tholeiite and olivine basalt are olivine at 1 Atmosphere, 4.5 kb and 9 kb, orthopyroxene at 13.5 and 18 kb, clinopyroxene at 22.5 kb and garnet at 27 kb. In the alkali olivine basalt composition, the liquidus phases are olivine at 1 Atmosphere and 9 kb, orthopyroxene with clinopyroxene at 13.5 kb, clinopyroxene at 18 kb and garnet at 27 kb. The sequence of appearance of phases below the liquidus has also been studied in detail. The electron probe micro-analyser has been used to make partial quantitative analyses of olivines, orthopyroxenes, clinopyroxenes and garnets which have crystallized at high pressure.These experimental and analytical results are used to determine the directions of fractionation of basaltic magmas during crystallization over a wide range of pressures. At pressures corresponding to depths of 35–70 km separation of aluminous enstatite from olivine tholeiite magma produces a direct fractionation trend from olivine tholeiites through olivine basalts to alkali olivine basalts. Co-precipitation of sub-calcic, aluminous clinopyroxene with the orthopyroxene in the more undersaturated compositions of this sequence produces derivative liquids of basanite type. Magmas of alkali olivine basalt and basanite type represent the lower temperature liquids derived by approximately 30% crystallization of olivine-rich tholeiite at 35–70 km depth. At depths of about 30 km, fractionation of olivine-rich tholeiite with separation of both olivine and low-alumina enstatite, joined at lower temperatures by sub-calcic clinopyroxene, leads to derivative liquids with relatively constant SiO₂ (48 to 50%) increasingly high Al₂O₃ (15–17%) contents and retaining olivine + hypersthene normative chemistry (5–15% normative olivine). These have the composition of typical high-alumina olivine tholeiites. The effects of low pressure fractionation may be superimposed on magma compositions derived from various depths within the mantle. These lead to divergence of the alkali olivine basalt and tholeiitic series but convergence of both the low-alumina and high-alumina tholeiites towards quartz tholeiite derivative liquids.The general problem of derivation of basaltic magmas from a mantle of peridotitic composition is discussed in some detail. Magmas are considered to be a consequence of partial melting but the composition of a magma is determined not by the depth of partial melting but by the depth at which magma segregation from residual crystals occurs. Magma generation from parental peridotite (pyrolite) at depths up to 100 km involves liquid-crystal equilibria between basaltic liquids and olivine + aluminous pyroxenes and does not involve garnet. At 35–70 km depth, basaltic liquids segregating from a pyrolite mantle will be of alkali olivine basalt type with about 20% partial melting but with increasing degrees of partial melting, liquids will change to olivine-rich tholeiite type with about 30% melting. If the depth of magma segregation is about 30 km, then magmas produced by 20–25% partial melting will be of high-alumina olivine tholeiite type, similar to the oceanic tholeiites occurring on the sea floor along the mid-oceanic ridges.Hypotheses of magma fractionation and generation by partial melting are considered in relation to the abundances and ratios of trace elements and in relation to isotopic abundance data on natural basalts. It is shown that there is a group of elements (including K, Ti, P, U, Th, Ba, Rb, Sr, Cs, Zr, Hf and the rare-earth elements) which show enrichment factors in alkali olivine basalts and in some tholeiites, which are inconsistent with simple crystal fractionation relationships between the magma types. This group of elements has been called incompatible elements referring to their inability to substitute to any appreciable extent in the major minerals of the upper mantle (olivine, aluminous pyroxenes). Because of the lack of temperature contrast between magma and wall-rock for a body of magma near to its depth of segregation in the mantle, cooling of the magma involves complementary processes of reaction with the wall-rook, including selective melting and extraction of the lowest melting fraction. The incompatible elements are probably highly concentrated in the lowest melting fraction of the pyrolite. The production of large overall enrichments in incompatible elements in a magma by reaction with and highly selective sampling of large volumes of mantle wall-rock during slow ascent of a magma is considered to be a normal, complementary process to crystal fractionation in the mantle. This process has been called wall-rock reaction. Magma generation in the mantle is rarely a simple, closed-system partial melting process and the isotopic abundances and incompatible element abundances of a basalt as observed at the earth's surface may be largely determined by the degree of reaction with the mantle or lower crustal wall-rocks and bear little relation to the abundances and ratios of the original parental mantle material (pyrolite).Occurrences of cognate xenoliths and xenocrysts in basalts are considered in relation to the experimental data on liquid-crystal equilibria at high pressure. It is inferred that the lherzolite nodules largely represent residual material after extraction of alkali olivine basalt from mantle pyrolite or pyrolite which has been selectively depleted in incompatible elements by wall-rock reaction processes. Lherzolite nodules included in tholeiitic magmas would melt to a relatively large extent and disintegrate, but would have a largely refractory character if included in alkali olivine basalt magma. Other examples of xenocrystal material in basalts are shown to be probable liquidus crystals or accumulates at high pressure from basaltic magma and provide a useful link between the experimental study and natural processes.  相似文献   

Coseismic and other short-term strain changes recorded with Sacks-Evertson strainmeters in a deep mine, South Africa   总被引：2，自引：0，他引：2  

A. McGarr  I. S. Sacks  A. T. Linde  S. M. Spottiswoode  R. W. E. Green 《Geophysical Journal International》1982,70(3):717-740

Summary. During 1977 March and April, three Sacks-Evertson borehole dilatometers were installed at the ends of boreholes drilled into the sidewall of an experimental tunnel at a depth of 3.1 km in the ERPM gold mine near Johannesburg. In the following year coseismic strain changes ranging from 5 ± 10⁻¹⁰ to values exceeding 5 ± 10⁻⁶ were recorded for hundreds of mine tremors in the magnitude range -1 to 3.7 and at hypocentral distances of 50 m to about 2 km. Hypocentral coordinates and magnitudes were determined from seismograms recorded from an underground array of geophones. Amplitudes and polarities of the coseismic strain steps are generally in excellent agreement with theoretical expectations based on point-source dislocation theory; specifically, the strain steps are proportional to the seismic moment divided by the cube of hypocentral distance. At a strain level of 5 ± 10⁻⁹ or greater the tremors do not appear to be preceded by any short-term indications of instability even for tremors producing coseismic steps greater than 5 ± 10⁻⁶ and for which the strainmeters were within a source radius of the hypocentre. Continuous strain changes observed at the times when the mine excavation, at a distance of about 100 m, is extended are in good agreement with calculated changes based on the theory of elasticity. A similar calculation is consistent with post-seismic strain changes observed to follow some of the closer tremors. These post-seismic strains show a logarithmic dependence on time following the tremor and appear to be due to the interaction of a tremor with the adjacent mine excavation rather than to deformation within the actual seismic source region.  相似文献   

The Magnetic Helicity Budget of a cme-Prolific Active Region     

Green  L.M.  López fuentes  M.C.  Mandrini  C.H.  Démoulin  P.  Van Driel-Gesztelyi  L.  Culhane  J.L. 《Solar physics》2002,208(1):43-68

Coronal mass ejections (CMEs) are thought to be the way by which the solar corona expels accumulated magnetic helicity which is injected into the corona via several methods. DeVore (2000) suggests that a significant quantity is injected by the action of differential rotation, however Démoulin et al. (2002b), based on the study of a simple bipolar active region, show that this may not be the case. This paper studies the magnetic helicity evolution in an active region (NOAA 8100) in which the main photospheric polarities rotate around each other during five Carrington rotations. As a result of this changing orientation of the bipole, the helicity injection by differential rotation is not a monotonic function of time. Instead, it experiences a maximum and even a change of sign. In this particular active region, both differential rotation and localized shearing motions are actually depleting the coronal helicity instead of building it. During this period of five solar rotations, a high number of CMEs (35 observed, 65 estimated) erupted from the active region and the helicity carried away has been calculated, assuming that each can be modeled by a twisted flux rope. It is found that the helicity injected by differential rotation (–7×10⁴² Mx²) into the active region cannot provide the amount of helicity ejected via CMEs, which is a factor 5 to 46 larger and of the opposite sign. Instead, it is proposed that the ejected helicity is provided by the twist in the sub-photospheric part of the magnetic flux tube forming the active region.  相似文献