Tidal contribution of the satellites to removing the angular momentum of Jupiter

Summary It has been shown that dynamically, on the basis of the distribution of angular momenta, the Jovian system cannot be considered an analogue within the Solar system. The total tidal decrease in the angular momentum of Jupiter and in its angular velocity of rotation have been estimated, as well as the loss of mechanical energy due to tidal dissipation. It has been concluded that there are no dynamical contradictions with the hypothesis of the common cosmogonic origin of Jupiter and of its eight close satellites.

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Impact of Urban Surroundings on Some Limnological Characteristics of a Tropical Aquatic Ecosystem

The water quality of an urban pond in the thickly populated area of Varanasi city (5 km apart) was studied and compared with a rural pond in the Banaras Hindu University campus for transparency, conductivity and nutrient richness (Cl^?, SO, PO? P, NO? N, organic carbon, Ca²⁺, Mg²⁺, K⁺, Na⁺) at three depths (surface, 1.5 m, 3 m) at monthly intervals between February 1982 and February 1983. This was done to assess the effects of urban surroundings of a very ancient city sector on pond water quality in reference to that of a rural pond. The rural pond had a lush growth of 12 macrophytic species, whereas the urban one had only such a growth with many phytoplanktonic species. Transparency was maximum in the winter season and the rural pond water was more transparent, while the electrolytical conductance was maximum in the rainy season, being higher in the urban pond. Electrolytical conductivity was negatively correlated to transparency: urban: EC = 1081.612–6.575 T, r² = 0.897, F_1,11 = 96, P <0.005; rural: EC = 728.981–4.328 T, r₂ = 0.892, F_1,11 = 91, P <0.005. Chloride and sulphate concentrations were highest in summer months, but the former was much higher in the urban pond while the latter in the rural pond. NO₃–N was highest in the rainy season in the rural pond and in early winter in the urban one and showed a definite trend with change in depth. PO₄–P also varied with depth and time and it was higher in late summer and the early rainy season in the rural pond and in early winter in the urban pond. But both these nutrients were much higher in the urban pond. The maximum organic carbon concentration was found in the rainy season in the rural pond and in summer months in the urban pond. The variation of organic carbon with depth was distinct. Both summer and winter seasons showed almost similar values of calcium concentration in the rural pond, but in the urban pond it was maximum in summer. Organic carbon and calcium were higher in the urban pond. The magnesium concentration was highest in rainy months in both the ponds, but the periodicity of the minimum differed. The distribution of calcium with depth was not well defined. The highest concentration of potassium was found in the winter season in both the ponds. The sodium concentration in the rural pond was observed maximum in summer and minimum in the rainy season, but in the urban pond the trend was different. The variation of potassium and sodium with depth was not well defined. Magnesium and sodium were also higher in the urban pond but potassium was almost at the same concentration in both the ponds. The effect of urbanisation may be one of the factors which might be responsible to the shift of the species composition towards phytoplanktonic flora.     

Ion microprobe analysis of oxygen isotope ratios in granulite facies magnetites: diffusive exchange as a guide to cooling history

Ion microprobe analysis of magnetites from the Adirondack Mountains, NY, yields oxygen isotope ratios with spatial resolution of 2–8 m and precision in the range of 1 (1 sigma). These analyses represent 11 orders of magnitude reduction in sample size compared to conventional analyses on this material and they are the first report of routinely reproducible precision in the 1 per mil range for analysis of ¹⁸O at this scale. High precision micro-analyses of this sort will permit wide-ranging new applications in stable isotope geochemistry. The analyzed magnetites form nearly spherical grains in a calcite matrix with diopside and monticellite. Textures are characteristic of granulite facies marbles and show no evidence for retrograde recrystallization of magnetite. Magnetites are near to Fe₃O₄ in composition, and optically and chemically homogeneous. A combination of ion probe plus conventional BrF₅ analysis shows that individual grains are homogeneous with ¹⁸O=8.9±1 SMOW from the core to near the rim of 0.1–1.2 mm diameter grains. Depth profiling into crystal growth faces of magnetites shows that rims are 9 depleted in ¹⁸O. These low ¹⁸O values increase in smooth gradients across the outer 10 m of magnetite rims in contact with calcite. These are the sharpest intracrystalline gradients measured to date in geological materials. This discovery is confirmed by bulk analysis of 150–350 m diameter magnetites which average 1.2 lower in ¹⁸O than coarse magnetites due to low ¹⁸O rims. Conventional analysis of coexisting calcite yields °¹⁸O=18.19, suggesting that bulk ¹⁸O (Cc-Mt)=9.3 and yielding an apparent equilibration temperature of 525° C, over 200° C below the temperature of regional metamorphism. Consideration of experimental diffusion data and grain size distribution for magnetite and calcite suggests two contrasting cooling histories. The data for oxygen in calcite under hydrothermal conditions at high P(H₂O) indicates that diffusion is faster in magnetite and modelling of the low ¹⁸O rims on magnetite would suggest that the Adirondacks experienced slow cooling after Grenville metamorphism, followed by a brief period of rapid cooling, possibly related to uplift. Conversely, the data for calcite at low P(H₂O) show slower oxygen diffusion than in magnetite. Modelling based on these data is consistent with geochronology that shows slow cooling through the blocking temperature of both minerals, suggesting that the low ¹⁸O rims form by exchange with late, low temperature fluids similar to those that infiltrated the rock to serpentinize monticellite and which infiltrated adjacent anorthosite to form late calcite veinlets. In either case, the ion microprobe results indicate that two distinct events are recorded in the post-metamorphic exchange history of these magnetites. Recognition of these events is only possible through microanalysis and has important implications for geothermometry.     

The redox states of basic and silicic magmas: a reflection of their source regions?

At present the best estimates of the oxygen fugacity of spinel-lherzolites that could be the source material of basic magmas is about five log units below the Ni–NiO buffer to one above it. However partially glassy basic lavas, ranging from MORBs to minettes, all with olivine on their liquidus, cover a wider range, and may have oxygen fugacities that extend to four log units above NNO. Surprisingly the range of oxygen fugacities observed in silicic lavas and ashflows with quartz phenocrysts is smaller, despite a crustal dominated evolution. The peralkaline silicic lava type pantellerite is the most reduced, equivalent to MORBs, whereas the large volume ashflows with phenocrysts of hornblende and/or sphene are the most oxidised. As the concentration of water in the basic lavas is correlated with increase in their redox state, it would seem that water could be the agent of this increase. That this is unlikely is seen in the behavior of silicic ashflows and lavas, particularly those of Yellowstone. Here the silicic magmas of the last 2Ma contain about 2 wt% FeO_(total), and typically phenocrysts of fayalite, quartz and Fe–Ti oxides. Despite extensive exchange of the ¹⁸O of the magma with meteoric water after caldera collapse (Hildreth et al. 1984), there is no displacement of the redox equilibria. Thus the thermal dissociation of molecular H₂O to H₂, and its subsequent diffusive loss to cause oxidation must have been minimal. This could only be so if the activity of water was small, as it would be if H₂O reacted with the silicate liquid to form OH groups (Stolper 1982). The conclusion is that silicic magmas with small amounts of iron and large amounts of water do not have their redox states reset, which in turn presumably reflect their generation. By analogy basic magmas with large amounts of iron and far less water are even less likely to have their redox equilibria disturbed, so that their oxygen fugacities will also reflect their source regions. The effect of pressure on the ferric-ferrous equilibrium in basic magmas can be calculated from experimental measurements of the partial molar volumes of FeO and Fe₂O₃, and their pressure derivatives V/P, in silicate liquids. The effect of pressure is found to be about the same on the liquid as it is for various solid oxygen buffers. Accordingly there should be mantle source regions covering the same range of oxygen fugacity as that found in basic lavas, but so far samples of spinel-lherzolite of equivalent oxygen fugacity to minettes or other potassic lavas have not been found. Whether or not the redox state of phlogopite-pyroxenites is equivalent to these potassic lavas cannot be established without experiment.     

Na-rich carbonate inclusions in perovskite and calzirtite from the Guli intrusive Ca-carbonatite,polar Siberia

Carbonate phases, some rich in Na₂O and comparatively rich in SrO and BaO, occur as inclusions in perovskite and calzirtite (Ca₂Zr₅Ti₂O₁₆) in the carbonatite of the Guli complex, Siberia. This is the first record of alkali carbonates, akin to nyerereite [Na₂Ca(CO₃)₂], in plutonic igneous rocks. The inclusion populations suggest that the parental magma of the complex was Ca-rich but developed Na-rich differentiates during the latest stages. This points to the dominant calcic carbonatites of the complex not being derivatives of alkali-rich parental carbonatites. These alkali-rich carbonate inclusions (and rare inclusions of djerfisherite) have been preserved due to the resistance of perovskite and calzirtite to processes of leaching, hydrothermal alteration and weathering.     

A field and theoretical analysis of garnet+chlorite+chloritoid+biotite assemblages from the tri-state (MA,CT, NY) area,USA

The prograde evolution of minerals in metapelites of a Barrovian sequence from the tri-state area (Massachusetts, Connecticut, New York) of the Taconic Range involves assemblages with garnet (Ga), chlorite (Ch), chloritoid (Ct), biotite (Bi) and staurolite (St). Detailed petrologic observations, mineral compositions and chemical zoning in garnet show: (1) garnet high in Mn and Fe but low in Mg is stable with chlorite at grades below those where chloritoid+biotite is found; (2) early formed garnet reacted partially to form Ct+Bi at intermediate grades; (3) at higher grades garnet (with low Mn)+chlorite is again produced, at the expense of chloritoid+biotite, suggesting a reversal in the continuous reaction involving the phases Ga, Ch, Ct and Bi. Thermodynamic modeling of the assemblage Ga+Ch+Ct+Bi±St in the MnKFMASH system reveals: (1) in the MnKFASH system the prograde reaction is Ga+Ch=Ct+Bi whereas in the KFMASH system the prograde reaction is the opposite: Ct+Bi=Ga+Ch; (2) the Ga–Ch–Ct–Bi–St invariant point in the KFMASH system occurs twice, at approximately 6.5 kbar, 545° C and 14.8 kbar, 580° C (although one of them may be metastable in a complex phase system); the appearance of the petrogenetic grid is markedly different from that of Albee, but similar to that of Spear and Cheney; (3) as a consequence, in the KFMASH system, chloritoid+biotite are stable over a wide range of P-T conditions whereas garnet+chlorite assemblages are restricted to a narrow band of P-T conditions; (4) MnO increases the stability field of Ga+Ch relative to both Ct+Bi at low temperatures, and St+Bi at high temperatures; (5) in natural samples the occurrence of Ct+Bi is controlled more by bulk Mg–Fe(-Mn) composition than P-T conditions. Specifically, Ct+Bi is restricted to bulk compositions with Fe/(Mg+Fe+Mn)>0.6. Rocks with Fe/(Mg+Fe+Mn)<0.5 are likely to display only chlorite+biotite at low grade. These observations are consistent with Wang and Spear and Spear and Cheney.     

An Example of Island-Arc Petrogenesis: Geochemistry and Petrology of the Southern Luzon Arc, Philippines

Volcanism throughout the Luzon arc is associated with eastwardsubduction of the South China Sea floor along the Manila Trench.The southern section of the arc, the focus of this study, extendsfrom the Lingayen-Dingalan fault to the small islands just southof Luzon. Two segments appear to exist along this section ofthe arc the northern Bataan and southern Mindoro segments whichare separated by the Macolod Corridor. The volcanic rocks have typical arc phenocryst mineralogies:olivine, clinopyroxene, plagioclase, and titanomagnetite inthe most mafic rocks and clinopyroxene, plagioclase, orthopyroxene,titanomagnetite, ? amphibole in the more felsic samples. Complexzoning, sieve textures, and decoupling of incompatible traceelements suggest that processes such as assimilation have takenplace. The rocks from the study area range from basalts to rhyolitesand show typical calc-alkaline features. The rocks of the MacolodCorridor and Mindoro segment are particularly enriched in largeion lithophile elements (LILE), light rare earth elements (LREE),and radiogenic Sr compared with the Bataan segment. The datafall within the mantle array on Sr-Nd isotopic diagrams andgrade toward higher Sr and lower Nd isotopic values from northto south. A likely source for the volcanics of this study is either amid-ocean ridge basalt (MORB)-type mantle that undergoes higherdegrees of partial melting than regions involved in MORB generationor a previously depleted source. We suggest that the high fieldstrength element (HFSE) anomalies have been derived throughdifferential element partitioning during fluid transport fromthe subducted lithosphere to the mantle wedge. Continental crustal material seems to play a significant roleparticularly in the Macolod Corridor and the Mindoro segment,based on the high LILE, La/Sm ratios, radiogenic Sr isotopes,and ¹⁸O values. The Macolod Corridor and the Mindoro segmenthave undergone source contamination by crustal material fromthe North Palawan-Mindoro crustal block either during the collisionof this block with the Manila Trench or by subduction of sedimentsrich in this crustal material. A similar component has alsobeen detected in the Bataan segment but in minor amounts. Thetrace element and isotopic differences between the northernand southern sections of the arc are interpreted in terms ofvariable composition (i. e., variable amounts of a crustal componentintroduced from the Palawan-Mindoro crustal terrain) of themetasomatic fluids released into the source.     

Geochemical specialization of the tin-bearing granitoid massifs of NW Bohemia

The geochemistry of Hercynian tin-bearing granitoid massifs of the Krune hory Mts. (Erzgebirge), Slavkovský les Forest (Kaiserwald) and Smriny (eastern Fichtelgebirge) is compared by statistical processing of 270 analyses including a wide spectrum of major and trace elements. Seven different types of granites are distinguished. Out of these, five types represent the successive differentiation of the largest massif of NW Bohemia: the Karlovy Vary (Karlsbad) massif. This comprises strongly differentiated peraluminous granites evolving towards extreme Li-Rb-Cs-F-and Sn-enrichment in the youngest members, which are albite-topaz-zinwaldite lithium granites. The sixth and seventh types are different from the former by their location in the eastern Krune hory and tectonic setting, and they display geochemical features of anorogenic granites: they are metaluminous albite-zinwaldite granites with marked enrichment of Nb, Y, and HREE in addition to Li, Rb, Cs, F and Sn, indicating contamination by sub-crustal material. Sn-W mineralizations, including flat peri-contact greisen bodies, steep greisen veins and tourmalinized phyllites, are all intimately associated with the most strongly differentiated granites — the Li-granite and the Cinovec-granite respectively.     

The effect of bulk rock composition on the stability of amphibole in the upper mantle: Implications for solidus positions and mantle metasomatism

Summary The stability of pargasitic amphibole in the upper mantle is a function of water content and bulk rock composition, and under water-undersaturated conditions, the stability of amphibole controls the solidus position. Experiments in the system Tinaquillo peridotite +0.2% H₂O, a refractory peridotite under water-undersaturated conditions, show that amphibole is stable to 1030°C and 26 kb. In contrast, pargasitic amphibole is stable to 1150°C and 30 kb in Hawaiian pyrolite, a more fertile peridotite composition. This indicates that under water-undersaturated conditions, the most fertile part of a crystallizing mantle diapir with an inhomogeneous composition will solidify first while a more refractory component will contain an alkali-rich melt which will have the ability to metasomatize adjacent regions. The relative stabilities of amphibole in refractory and fertile bulk compositions may result in increasing rather than diminishing chemical contrasts in high temperature lherzolite, i.e. a process of metamorphic differentiation. Ti, Fe, Al and Na metasomatism can therefore be considered a normal occurrence associated with the upward migration and solidification of an H₂O-bearing mantle diapir.

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Der Einfluß der Gesamtgesteins-Zusammensetzung auf die Stabilität von Amphibol im oberen Mantel: Bedeutung für Solidus-Positionen und Mantel-Metasomatose

Zusammenfassung Die Stabilität pargasitischer Amphibole im oberen Mantel ist eine Funktion von Wassergehalt und Gesamtgesteins-Zusammensetzung. Unter wasser-untersättigten Bedingungen, kontrolliert die Stabilität von Amphibol die Solidus-Position. Experimente in dem System Tinaquillo Peridotit +0,2% H₂O, einem refraktären Peridotit unter wasser-untersättigten Bedingungen, zeigen daß Amphibol bis 1030°C und 26 Kb stabil ist. Im Gegensatz dazu ist pargasitische Hornblende in einem Hawaii-Pyrolit, von mehr fertiler Peridotit-Zuammensetzung, bis 1150°C und 30 Kb stabil. Das zeigt, daß bei wasser-untersättigten Bedingungen der am meisten produktive Teil eines kristallisierenden Mantel-Diapirs mit inhomogener Zusammensetzung sich zuerst verfestigen wird, während eine mehr refraktäre Komponente eine alkali-reiche Schmelze enthalten wird, die wiederum die Fähigkeit hat, umliegende Bereiche metasomatisch zu beeinflussen. Die relativen Stabilitäten von Amphibol in refraktären und fertilen Gesamtzusammensetzungen können dazu führen, daß die chemischen Gegensätze in Hochtemperaturlherzoliten eher zunehmen als abnehmen, d. h. ein Prozeß metamorpher Differentiation. Ti, Fe, Al und Na Metasomatose können deshalb als ein verbreiteter Vorgang, der mit der Aufwärtsbewegung und Verfestigung eines H₂O-führenden Mantel-Diapirs assoziiert ist, betrachtet werden.

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With 4 Figures