Estimation of earthquake source parameters in the Kachchh seismic zone,Gujarat, India,using three component S-wave spectra

Earthquake source parameters and crustal \(Q_{0}\) values for the 138 selected local events of (\(\hbox {M}_{\mathrm{w}}{:}2.5{-}4.4\)) the 2001 Bhuj earthquake sequence have been computed through inversion modelling of S-waves from three-component broadband seismometer data. SEISAN software has been used to locate the identified local earthquakes, which were recorded at least three or more stations of the Kachchh seismological network. Three component spectra of S-wave are being inverted by using the Levenberg–Marquardt non-linear inversion technique, wherein the inversion scheme is formulated based on \(\omega ^{2}\) source model. SAC Software (seismic analysis code) is being utilized for calculating three-component displacement and velocity spectra of S-wave. The displacement spectra are used for estimating corner frequency (in Hz) and long period spectral level (in nm-s). These two parameters play a key role in estimating earthquake source parameters. The crustal \({Q}_{0}\) values have been computed simultaneously for each component of three-component broadband seismograph. The estimated seismic moment (\(M_{0}\)) and source radius (r) using S-wave spectra range from 7.03E+12 to 5.36E+15 N-m and 178.56 to 565.21 m, respectively. The corner frequencies for S-wave vary from 3.025 to 7.425 Hz. We also estimated the radiated energy (\(E_{S}\)) using velocity spectra, which is varying from 2.76E+06 to 4.07E+11 Joules. The estimated apparent stress drop and static stress drop values range from 0.01 to 2.56 and 0.53 to 36.79 MPa, respectively. Our study also reveals that estimated \(Q_{0}\) values vary from 119.0 to 7229.5, with an average \(Q_{0}\) value of 701. Another important parameter, by which the earthquake rupture process can be recognized, is Zuniga parameter. It suggests that most of the Kachchh events follow the frictional overshoot model. Our estimated static stress drop values are higher than the apparent stress drop values. And the stress drop values are quite larger for intraplate earthquakes than the interplate earthquakes.     

Geochemical characteristics of the lower part of Shayi Member in Lixian Slope,Raoyang Sag,Bohai Bay Basin,Northern China: Implications for organic matters origin,thermal maturity and depositional environment

The lower part of Shayi Member (Es1x Sub-Member) composed mainly of dark mudstones and shales is the dominant source rocks for the Lixian Slope. Based on organic petrology, organic and inorganic geochemistry analyses of several mudstone and shale samples selected from Es1x Sub-Member, this research provides an overview on type, origin and thermal maturity of organic matters, as well as depositional environment of Es1x Sub-Member. Kerogen microscopy observation shows that the macerals are dominated by sapropelinite with a significant mixture of vitrinite and inertinite, indicating that aquatic algal-bacterial organic matter inputs are dominate with a significant contribution of terrigenous organic matter inputs. This statement is supported by n-alkane patterns distribution characteristics, high (n-C₂₁ + n-C₂₂)/(n-C₂₈ + n-C₂₉) values (average = 1.77), the plot of high Ph/n-C₁₈ values (average = 4.15) versus low Pr/n-C₁₇ values (average = 1.13), and high proportion of C₂₇ sterane and C₂₉ sterane (average = 37.7 and 42.0%, respectively). In addition, the rather low Pr/Ph values (average = 0.38), high gammacerane index values (average = 0.30), high V/Ni and V/(V + Ni) values (average = 11.84 and 0.89, respectively), high Sr/Ba and Sr/Cu values (average = 8.54 and 108, respectively), indicative of a saline water condition and a anoxic depositional environment. The low C29 sterane ααα 20S/(20S + 20R), C₂₉ sterane αββ/(αββ + ααα), C₃₁ homohopane 22S/(22S + 22R), C₃₂ homohopane 22S/(22S + 22R), Ts/(Ts + Tm) values and relatively high moretane/hopane values show that the level of thermal maturity of organic matters in Es1x Sub-Member are low.     

Genesis of copper mineralisation,Myall Creek prospect,South Australia

The Myall Creek copper prospect is in unmetamorphosed carbonaceous dolosiltstone and sandstone at the base of the late Proterozoic (Adelaidean) Tapley Hill Formation. It contains disseminated, fine-grained chalcopyrite, zincian tennanite, bornite, chalcocite, pyrite, sphalerite and galena, and irregular to straight chalcopyrite-rich veinlets. Some ore minerals rim and/or partially replace pyrite or clastic grains. There is no evidence of hydrothermal activity. The ³⁴S_CDT values of pyrite and the other sulfides fall in the wide range –3.6 to +44.2. Dolomite in both mineralised and unmineralised samples has ¹³C_PDB values concentrated around –3, and ¹⁸O_SMOW values around +25. It is concluded that the mineralising fluids were near-neutral brines which leached metals from the basement and early Adelaidean rocks. They entered the Tapley Hill sediments at moderately low temperatures via permeable strata and faults. The metals were precipitated by biogenic H₂S, and also fixed by reaction with iron sulfides and, possibly, organic matter. Continuing ascent of brines into the mineralised strata caused breakdown of detrital feldspars and Fe-Ti oxides, and some solution-remobilisation of early-formed sulfides.     

1993 COMPILATION OF DATA ON FIVE BELGIAN SEDIMENTARY ROCK REFERENCE MATERIALS: AWI-1, SBO-1, PRI-1, CCH-1 AND DWA-1

Five Belgian sedimentary rock reference materials have been prepared and distributed by the Geology, Petrology and Geochemistry Laboratory (Liège University, Belgium). Thirty-six laboratories participated in the international co-operative study. The individual data received from the participating laboratories are listed. Tables of compiled results are presented for major, minor and trace elements. These updated values are summarized into means, associated standard deviations, medians, and concentration ranges. "Recommended" (or proposed) values are presented.     

Upper temperature tolerance of spot,Leiostomus xanthurus,from the cape Fear River estuary,North Carolina

The temperature tolerance and resistance times of postlarval (<25 mm SL) and small juvenile spot,Leiostomus xanthurus, from the Cape Fear Estuary, North Carolina were tested in the laboratory. Critical thermal maximum techniques were used to determine first equilibrium loss (FEL) and critical thermal maximum (CTM) end points and thermal shock methods were used to determine 96-h upper incipient lethal temperatures (LT₅₀). Acclimation temperatures ranged from 10 to 35°C and acclimation salinities were 10, 20 and 30‰. A quadratics model was fit to the CTM and FEL data; r² values were 0.924 and 0.928 respectively. Acclimation salinity, estimated weight, acclimation salinity by acclimation temperature interaction and acclimation temperature by estimated weight interaction were the significant components of the CTM model. Predicted CTM values ranged from 30°C at 10 °C and 30‰ acclimation to just over 40°C at 30 °C and 30‰ acclimation. Acclimation temperature, acclimation temperature squared, estimated weight and acclimation temperatures by estimated weight interaction were the significant components of the FEL model. Predicted FEL values ranged from around 28°C at 10°C and 10‰ acclimation to about 39°C at 30°C and 30‰ acclimation. The 96-h LT₅₀ values of spot acclimated to 20‰ increased linearly with acclimation temperature to 25°C. From about 25 to 35°C, LT₅₀ values increased very little with acclimation temperature. The ultimate upper incipient lethal temperature of postlarval and small juvenile spot was estimated at 35.2°C. Increased salinity increased resistance time but decreased LT₅₀ estimates. Thermal shock tests were better for predicting the effects of thermal addition than were CTM tests.     

Crystal-melt partitioning of noble gases (helium, neon, argon, krypton, and xenon) for olivine and clinopyroxene

Mineral-melt partition coefficients of all noble gases (^min/meltD_i) have been obtained for olivine (ol) and clinopyroxene (cpx) by UV laser ablation (213 nm) of individual crystals grown from melts at 0.1 GPa mixed noble gas pressure. Experimental techniques were developed to grow crystals virtually free of melt and fluid inclusions since both have been found to cause profound problems in previous work. This is a particularly important issue for the analysis of noble gases in crystals that have very low partition coefficients relative to coexisting melt and fluid phases. The preferred partitioning values obtained for the ol-melt system for He, Ne, Ar, Kr, and Xe are 0.00017(13), 0.00007(7), 0.0011(6), 0.00026(16), and , respectively. The respective cpx-melt partition coefficients are 0.0002(2), 0.00041(35), 0.0011(7), 0.0002(2), and . The data confirm the incompatible behaviour of noble gases for both olivine and clinopyroxene but unlike other trace elements these values show little variation for a wide range of atomic radius. The lack of dependence of partitioning on atomic radius is, however, consistent with the partitioning behaviour of other trace elements which have been found to exhibit progressively lower dependence of ^min/meltD_i on radius as the charge decreases. As all noble gases appear to exhibit similar ^min/meltD_i values we deduce that noble gases are not significantly fractionated from each other by olivine and clinopyroxene during melting and fractional crystallisation. Although incompatible, the partitioning values for noble gases also suggest that significant amounts of primordial noble gases may well have been retained in the mantle despite intensive melting processes. The implication of our data is that high primordial/radiogenic noble gas ratios (³He/⁴He, ²²Ne/²¹Ne, and ³⁶Ar/⁴⁰Ar) characteristic of plume basalt sources can be achieved by recycling a previously melted (depleted) mantle source rather than reflecting an isolated, non-degassed primordial mantle region.     

Hydrothermal alteration and REE-Th mineralization at the Rodeo de Los Molles deposit,Las Chacras batholith,central Argentina

REE (rare-earth-element) and Th mineralization at the Rodeo de Los Molles deposit occurs within an elliptical body of hydrothermally altered rocks (fenite) located in a biotite monzogranite of the Las Chacras batholith. Ore assemblages are found as isolated patches of intergrown britholite, allanite, apatite, bastnaesite, fluorite, sphene, quartz, and aegirine-augite, as well as nodules of uranothorite and late-stage veins of calcite, fluorite, and bastnaesite. Composition-volume computations suggest that the fenite was produced by alteration of the biotite monzogranite by addition of K and Na, and loss of Ca and Sr. Petrographic evaluations indicate that microcline and plagioclase have been replaced by perthite, and biotite was converted to aggregates of clinochlore, anatase, kaolinite, and hematite. Relict biotite is characterized by lower Fe/(Fe+Mg) and Ti values with progressive alteration. Fluorine-rich phlogopite is present in mineralized areas, but textural evidence suggests that it was not produced via biotite alteration. Mass-balance constraints also show that Ca and Mg in ore zones may result from redistribution, rather than their being a result of external derivation. The ¹⁸O values of quartz (8.6–11.1) and feldspar (7.8–10.6) suggest that feldspar continued to exchange oxygen isotopes with a fluid to lower temperatures than did quartz. Feldspars equilibrated with a fluid of ¹⁸O8 at a fluid/rock ratio less than 1. The ¹⁸O values of quartz and aegirine-augite that crystallized during REE mineralization also suggest equilibration with a fluid of ¹⁸O8. The D values of biotite (-83 to-120) are relatively low for igneous rocks and are thought to have resulted from exsolution of a D-enriched magmatic vapor. The D values of both mineralized and barren fenites are consistent with equilibration with fluid of magmatic origin. Meteoric water was involved in the production of calcite and clinochlore alteration, and late-stage calcite-fluorite-bastnaesite veins. The ¹³C values of calcite and bastnaesite (-7.8 to-13.5%) suggest that carbon was derived by leaching of carbon from igneous and/or enclosing metamorphic rock types, and that a majority of carbon ultimately was derived from sedimentary organic meterial.     

Giant calcite-cemented concretions, Dakota Formation, central Kansas, USA

Giant spheroidal concretions (cannonball concretions; some nearly 6 m in diameter) in fluvial channel‐fill sandstones at two localities of the Dakota Sandstone formed by import of cement constituents at a burial depth of <1 km. During cannonball concretion growth a self‐organizational process restricted concretions to a relatively few but widely spaced, and locally, evenly spaced, sites. Other forms of calcite cements at these localities are cement patches in the form of intergrown grape‐size concretions (grapestone), and, locally, pervasive cement. An early episode of invasion by thermogenically generated H₂S, which reacted with iron oxides on detrital grains, generated scattered pyrite crystals and decimetre‐scale spheroidal pyrite concretions. Intergranular volumes (IGV) in the concretions range from 36% to 27%. The absence of a trend in IGV and of carbon and oxygen‐isotope ratios from cannonball centres to margins indicates that these concretions did not cement progressively outwards from the centre. Rather, the modern spheres represent the spatial extent of nucleation sites that were not otherwise organized within that volume. Carbon and oxygen‐isotope values for concretion calcites plot along a swath between depleted values of δ18C of ?36‰ and δ18O of ?13‰ and enriched values of ?4‰ and ?6‰, respectively. Four groups of calcites are evident on the basis of trace‐element content and suggest that the calcite precipitated across a range of oxidation conditions that do not correlate strongly with the isotopic compositions. Although fluvial overbank sandstones have some pedogenic calcite, the channel sandstones have at most a trace of pedogenic calcite and carbonate rock fragments, so that the bulk of cement components were imported to the sandstones. Carbon and calcium sources for calcite cement include marine limestone, carbonate shells, and anhydrite in addition to HCO derived from oxidized methane, most likely derived from beds underlying or laterally in communication with Dakota sandstones. HCO in ascending formation waters, released during compaction, mixed with meteoric water whose temperature and composition varied with time, to generate the 7‰ range in δ18O_calcite values measured.     

A sulphur isotope study of the Broken Hill deposit,New South Wales,Australia

Sulphur isotopic compositions of sulphides within garnet-rich rocks and high-grade ore from the Broken Hill deposit, New South Wales, Australia, have been determined and show a range of values of –3.3 to +6.7 per mil. Thermochemical considerations, including the spread of values of ³⁴S, suggest that the deposit was derived from a mixed source of sulphur in which seawater, reduced by inorganic processes, mixed with magmatic sulphur or that sulphate from contemporaneous seawater was reduced biogenically at low temperatures. Thermochemical considerations also suggest that pyrrhotite formed by desulphidation of pyrite so that the original Fe-S-O assemblage was pyrite ± magnetite.³⁴S measurements show a broad range which is considered to be due to isotopic reequilibration during retrograde metamorphism and analytical and sampling technique. These data should not be used to indicate original temperatures of deposition or metamorphic temperatures associated with the various metamorphic events.     

Marine hdrothermal alteration at a Kuroko ore deposit,Kosaka, Japan

Isotopic compositions were determined for quartz, sericite and bulk rock samples surrounding the Uwamuki no. 4 Kuroko ore body, Kosaka, Japan. ¹⁸O values of quartz from Siliceous Ore (S.O.), main body of Black Ore B.O.) and the upper layer of B.O. are fairly uniform, +8.7 to +10.5. Formation temperatures calculated from fractionation of ¹⁸O between sericite and quartz from B.O. and upper S.O. are 250° to 300° C. The ore-forming fluids had ¹⁸O values of +1 and D values of –10, from isotope compositions of quartz and sericite.Tertiary volcanic rocks surrounding the ore deposits at Kosaka have uniform ¹⁸O values, +8.1±1.0 (n=50), although their bulk chemical compositions are widely varied because of different degrees of alteration. White Rhyolite, which is an intensely altered rhyolite occurring in close association with the Kuroko ore bodies, has also uniform ¹⁸O values, +7.9±0.9 (n=19). Temperatures of alteration are estimated to be around 300° C from the oxygen isotope fractionation between quartz and sericite. Paleozoic basement rocks phyllite and chert, have high ¹⁸O values, +18 and +19. The Sasahata formation of unknown age, which lies between Tertiary and Paleozoic formations, has highly variable ¹⁸O, +8 to +16 (n=4). High ¹⁸O values of the basement rocks and the sharp difference in ¹⁸O at their boundary suggest that the hydrothermal system causing Kuroko mineralization was mainly confined within permeable Tertiary rocks. D values of altered Tertiary volcanic rocks are highly variable ranging from –34 to –64% (n=12). The variation of D does not correlate with change of chemical composition, ¹⁸O values, nor distance from the ore deposits. The relatively high D values of the altered rocks indicate that the major constituent of the hydrothermal fluid was sea water. However, another fluid having lower D must have also participated. The fluid could be evolved sea water modified by interaction with rocks and the admixture of magmatic fluid. The variation in D may suggest that sea water mixed dispersively with the fluid.     

Stable isotope and fluid inclusion studies of carbonate deposits from the Tolfa Mountains mining district (Latium,central Italy)

Carbon and oxygen isotope analyses were made of representative samples of calcite and quartz from the carbonate deposits in the Tolfa Mountains mining district. Measurements were also made of hydrogen isotope compositions, filling temperatures and salinities of fluid inclusions in these minerals. There are three stages of mineralization at Tolfa. In stage I, characterized by calc-silicate hornfels, the carbonates have relatively high ¹⁸O values of 14.5 to 21.6 suggesting a rather low water/rock ratio. ¹³C values of –0.3 to 2.1 indicate that appreciable decarbonation or introduction of deep-seated carbon did not occur. Stage II is marked by phanerocrystalline carbonates; ¹⁸O values of 13.1 to 20.0 and ¹³C values of 0.7 to 5.0 identify them as hydrothermal veins rather than marbles. D values of –56 to –50 for inclusion fluids suggest a possible magmatic component to the hydrothermal fluid. Filling temperatures of coarse-grained samples of Calcite II are 309° to 362° C with a salinity range of 5.3 to 7.1 weight percent NaCl. Calculated ¹⁸O values of 11–12 for these fluids are again indicative of low water/rock ratios. The sparry calcites of stage III have ¹⁸O and ¹³C values of 8.1 to 12.9 and –1.7 to 3.2, respectively. D values of inclusion fluids are –40 to –33, clearly heavier than in earlier stages and similar to values of modern local ground waters. A salinity measurement of <0.1 weight percent NaCl in a sample of Calcite III is compatible with a relatively unaltered ground water origin for this fluid. Precipitation of the sparry calcite took place at much lower temperatures, around 160° C. For quartz, ¹⁸O values of 9.3 to 12.4 and D values for inclusions of –53 to –28 are consistent with its late occurrence and paragenetic link with associated carbonates.     

Geology and geochemistry of the Changba SEDEX Pb-Zn deposit,Qinling orogenic belt,China

The Changba Pb-Zn SEDEX deposit occurs in the Middle Devonian sequence of the Anjiaca Formation of the Western Qinling Hercynian Orogen in the Gansu Province, China. The Changba-II orebody is hosted in biotite quartz schist and is the largest of 143 stratiform orebodies that are hosted either in biotite quartz schist or marble. The Changba-II comprises two types of mineralization: a bedded facies and an underlying breccia lens. The bedded section exhibits three sulfide sub-facies zoned from bottom to top: 1) banded sphalerite intercalated with quartz albitite; 2) interbedded massive pyrite and sphalerite ore; and 3) banded sphalerite ore intercalated with banded baritite. Major metallic minerals are sphalerite, pyrite, galena, with minor arsenopyrite, pyrrhotite, boulangerite, and rare chalcopyrite. The bedded sulfides are underlain by a lens of brecciated and albitized biotite-quartz schists cemented by sulfides and tourmaline.Massive and bedded sulfide ³⁴S values range from 8.1 to 29.3, whereas barite ³⁴S values range from 20.8 to 31.5. Disseminated pyrite in footwall schists has ³⁴S values ranging from 8.1 to 10.6, and increase to values ranging from 11.1 to 14.7 in the hangingwall. The lower ³⁴S values for massive and bedded sulfides are interpreted to be derived from progressive bacterial sulfate reduction (BSR) of Devonian seawater in a sulfate-restricted sub-basin. The higher ³⁴S values for massive and bedded sulfides could be a product of quantitative BSR but this is incompatible with barite being more abundant above the bedded sulfides. Instead, it is more likely that thermochemical sulfate reduction of seawater sulfate or of evaporite was the source of heavy hydrothermal sulfur. Heavy hydrothermal sulfur was injected into a sulfate-restricted sub-basin where it mixed with low ³⁴S BSR sulfide to form the massive and bedded sulfides. The REE patterns of sulfide layers and associated quartz albitite and baritite are similar to those of the host biotite quartz schists, suggesting that the hydrothermal fluids leached REE from the underlying rocks. Pb isotope ratios in galena form an array between the Upper Crust and the Mantle reservoir curves, which indicates that the lead is derived from upper crustal rocks comprising mafic igneous units. The Sr⁸⁷/Sr⁸⁶ ratio of 0.7101 for carbonate within the sulfide layers also suggests that Sr is derived from the mixing of Sr leached from upper crustal rocks with Middle Devonian seawater Sr. A Rb-Sr isochron age of 389.4 ± 6.4 Ma for sulfide layers and the interbedded hydrothermal sediments is consistent with the age of host Mid-Devonian strata. Ar³⁹/Ar⁴⁰ plateau age at 352.8 ± 3.5 Ma and Ar³⁹-Ar⁴⁰ isochron age of 346.6 ± 6.4 Ma for albite in the quartz albitite intercalated with sulfide layers indicate either albite formation after the sulfides or thermal resetting of the Rb-Sr system at about 350 Ma, the age of collision between the North China and Yangtze cratons.Editorial handling: E. Frimmel     

Radioelement (U,Th, Rn) concentrations in Norwegian bedrock groundwaters

Twenty-eight samples of groundwater from bedrock boreholes in three distinct Norwegian geological provinces have been taken and analyzed for content of Rn, U, and Th, together with a wide variety of minor and major species. Median values of 290 Bq/1, 7.6 g/1, and 0.02 g/1 were obtained for Rn, U, and Th respectively, while maximum values were 8500 Bq/1, 170 g/1, and 2.2 g/1. Commonly suggested drinking water limits range from 8 to 1000 Bq/1 for radon and 14 to 160 g/1 for uranium. Radioelement content was closely related to lithology, the lowest concentrations being derived from the largely Caledonian rocks of the Trøndelag area, and the highest from the Precambrian Iddefjord Granite of southeast Norway (11 boreholes) where median values of 2500 Bq/1, 15 g/1 and 0.38 g/1, respectively, were obtained. The Iddefjord Granite is not believed to be unique in Norway in yielding high dissolved radionuclide contents in groundwaters, and several other granitic aquifers warrant further investigation in this respect.     

O,H, C isotope study of rocks from the KTB pilot hole: crustal profile and constraints on fluid evolution

The pilot hole of the Continental Deep Borehole (KTB) drilling project is located in the Bavarian Oberpfalz at the western margin of the Bohemian Massif. The 4-km deep borehole penetrated various paragneisses and minor orthogneisses with intercalations of amphibolites and metagabbros. The different lithologies have systematically different whole-rock oxygen isotope values and give little evidence for large scale water-rock interaction. Minor fluid interaction is well documented during retrograde metamorphism by non-equilibrium fractionations between refractory minerals (quartz, garnet and hornblende) and altered minerals (chlorite/biolite and feldspar). Ubiquitous vein mineralisation indicates fluid-induced retrogression at temperatures between 150°C and 400°C. The D values of hydroxylbearing minerals are very uniform in all lithologic units. The calculated hydrogen isotope composition of the fluid in equilibrium with matrix and vein minerals increases from -45 for metabasic rocks, to -20 for gneisses, to about -5 for vein minerals. The oxygen isotope composition of the fluid has been buffered by the rock and decreases with decreasing temperature because of increasing fractionations at low temperatures and low water-rock ratios. Modern fluids sampled from open cavities within the borehole have isotopic compositions that suggest a continuous fluid evolution during retrogression in a closed system. The ¹³C values of calcite and graphite also indicate closed system mixing processes.     

Analytical Data on Three Rock Reference Samples from the Institute of Geochemistry, Irkutsk, USSR

Analytical data obtained in our two laboratories on three rook samples from the Institute of Geochemistry, Irkutsk, are reported and compared with "established", "certified" and "uncertain" values. Methods used are described briefly and some comments offered on earlier published information.     

H,O, Sr,Nd, and Pb isotope geochemistry of the Latir volcanic field and cogenetic intrusions,New Mexico,and relations between evolution of a continental magmatic center and modifications of the lithosphere

Over 200 H, O, Sr, Nd, and Pb isotope analyses, in addition to geologic and petrologic constraints, document the magmatic evolution of the 28.5–19 Ma Latir volcanic field and associated intrusive rocks, which includes multiple stages of crustal assimilation, magma mixing, protracted crystallization, and open- and closed-system evolution in the upper crust. In contrast to data from younger volcanic centers in northern New Mexico, relatively low and restricted primary ¹⁸O values (+6.4 to +7.4) rule out assimilation of supracrustal rocks enriched in ¹⁸O. Initial ⁸⁷Sr/⁸⁶Sr ratios (0.705 to 0.708), ¹⁸O values (-2 to-7), and ²⁰⁶Pb/²⁰⁴Pb ratios (17.5 to 18.4) of metaluminous precaldera volcanic rocks and postcaldera plutonic rocks suggest that most Latir rocks were generated by fractional crystallization of substantial volumes of mantle-derived basaltic magma that had near-chondritic Nd isotope ratios, accompanied by assimilation of crustal material in two main stages: 1) assimilation of non-radiogenic lower crust, followed by 2) assimilation of middle and upper crust by inter-mediate-composition magmas that had been contaminated during the first stage. Magmatic evolution in the upper crust peaked with eruption of the peralkaline Amalia Tuff (26 Ma), which evolved from metaluminous parental magmas. A third stage of late, roofward assimilation of Proterozoic rocks in the Amalia Tuff magma is indicated by trends in initial ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios from 0.7057 to 0.7098 and 19.5 to 18.8, respectively, toward the top of the pre-eruptive magma chamber. Highly evolved postcaldera plutons are generally fine grained and are zoned in initial ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios, varying from 0.705 to 0.709 and 17.8 to 18.6, respectively. In contrast, the coarser-grained Cabresto Lake (25 Ma) and Rio Hondo (21 Ma) plutons have relatively homogeneous initial ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios of approximately 0.7053 and 17.94 and 17.55, respectively. ¹⁸O values for all the postcaldera plutons overlap those of the precaldera rocks and Amalia Tuff, except for those for two late-stage rhyolite dikes associated with the Rio Hondo pluton that have ¹⁸O values of-8.6 and-9.5; these dikes are the only Latir rocks which may be largely crustal melts.Chemical and isotopic data from the Latir field suggest that large fluxes of mantle-derived basaltic magma are necessary for developing and sustaining large-volume volcanic centers. Development of a detailed model suggests that 6–15 km of new crust may have been added beneath the volcanic center; such an addition may result in significant changes in the chemical and Sr and Nd isotopic compositions of the crust, although Pb isotope ratios will remain relatively unchanged. If accompanied by assimilation, crystallization of pooled basaltic magma near the MOHO may produce substantial cumulates beneath the MOHO that generate large changes in the isotopic composition of the upper mantle. The Latir field may be similar to other large-volume, long-lived intracratonal volcanic fields that fundamentally owe their origins to extensive injection of basaltic magma into the lower parts of their magmatic systems. Such fields may overlie areas of significant crustal growth and hybridization.     

Resetting of oxybarometers and oxygen isotope ratios in granulite facies orthogneisses during cooling and shearing,Adirondack Mountains,New York

The petrography, petrology, and oxygenisotope geochemistry of granulite-facies granitic and syenitic orthogneisses of the Diana and Stark complexes, Adirondack Mountains, New York, show that the extent and nature of resetting of isotopic and mineralogic systems is highly variable. There is a strong correlation between retrogression and shearing, and the rocks may be divided texturally into: (1) unsheared lithologies that preserve little-retrogressed pyroxene-or hornblendebearing peak-metamorphic mineralogies; and (2) sheared rocks that underwent retrogression, marked by the growth of late biotite, in centimetre-to metre-wide shear zones after the peak of metamorphism. Oxygen fugacities in the unsheared lithologies were estimated for reintegrated mineral compositions from magnetiteilmenite (Mt-Ilm) and ferrosilite-magnetic-quartz (Fs-Mt-Qtz) equilibria. Mt-Ilm yields logfO_2Mt-Ilm values of-15.9 to-17.6 (0.6 to 1.3 log units below the fayalite-magnetite-quartz buffer, FMQ) and temperatures of 670–745°C that agree with those from other geothermometry and phase equilibria studies. These data suggest that, aside from oxyexsolution of ilmenite from magnetite, the Fe-Ti system underwent only minor resetting during cooling, and the Fe-Ti oxides yield good estimates of peak-metamorphic temperatures and fO₂. In unsheared ilmenite + magnetite + orthopyroxene + quartz assemblages, values of logfO_2Mt-Ilm are lower than logfO_2Fs-Mt-Qtz by an average of 0.6 when the orthopyroxene activity model of Sack and Ghiorso is used. Minor resetting of the Fe-Ti oxides, analytical errors, and errors in the placement of end-member reactions probably account for this relatively small difference in fO₂ values. Whole-rock ¹⁸O values of unsheared Diana and Stark lithologies range from 4.0 to 10.3 reflecting pre-regional metamorphic oxygen-isotope ratios. Peak-metamorphic minerals preserve high-temperature oxygen-isotope fractionations, and, in many samples, the effective diffusion of oxygen in minerals ceased at higher temperatures than predicted from wet experimental diffusion data. These data suggest that the rocks did not contain an aqueous fluid phase during cooling. The combination of petrologic, isotopic, and textural data also permits a detailed study of shearing and retrogression. Ilmenites in the sheared lithologies underwent greater degrees of hematite loss than in the unsheared rocks, resulting in logfO_2Mt-Ilm values as low as-24.1 (3.1 log units below FMQ) and Mt-Ilm temperatures that are up to 175°C below regional estimates. Sheared rocks also have higher ¹⁸O values (up to 13.3). During shearing, ¹⁸O values of biotite, K-feldspar, and magnetite reset readily, while the degree of isotopic resetting of quartz correlates with the intensity for recrystallization.This paper is a contribution to IGCP Project 304, Lower Crustal Processes     

Stable isotopic evidence for large-scale seawater infiltration in a regional metamorphic terrane; the Trois Seigneurs Massif,Pyrenees, France

Oxygen isotopic analyses of 95 metamorphic and igneous rocks and minerals from a Hercynian metamorphic sequence in the Trois Seigneurs Massif, Pyrenees, France, indicate that all lithologies at higher metamorphic grades than the andalusite in isograd have relatively homogeneous ¹⁸O values. The extent of homogenization is shown by the similarity of ¹⁸O values in metacarbonates, metapelites and granitic rocks (+11 to +13), and by the narrow range of oxygen isotopic composition shown by quartz from these lithologies. These values contrast with the ¹⁸O values of metapelites of lower metamorphic grade ( ¹⁸O about +15). Homogenization was caused by a pervasive influx of hydrous fluid. Mass-balance calculations imply that the fluid influx was so large that its source was probably high-level groundwaters or connate formation water. Hydrogen isotopic analyses of muscovite from various lithologies are uniform and exceptionally heavy at D=–25 to –30, suggesting a seawater origin. Many lines of petrological evidence from the area independently suggest that metamorphism and anatexis of pelitic metasediment occurred at depths of 6–12 km in the presence of this water-rich fluid, the composition of which was externally buffered. Deep penetration of surface waters in such environments has been hitherto unrecognized, and may be a key factor in promoting major anatexis of the continental crust at shallow depth. Three types of granitoid are exposed in the area. The leucogranites and the biotite granite-quartz diorite are both mainly derived from fusion of local Paleozoic pelitic metasediment, because all these rocks have similar whole-rock ¹⁸O values (+11 to +13). The post-metamorphic biotite granodiorite has a distinctly different ¹⁸O (+9.5 to +10.0) and was probably derived from a deeper level in the crust. Rare mafic xenoliths within the deeper parts of the biotite granite-quartz diorite also have different ¹⁸O (+8.0 to +8.5) and possibly represent input of mantle derived magma, which may have provided a heat source for the metamorphism.Contribution No. 4192, Publications of the Division of Geological and Planetary Sciences, California Institute of Technology     

1992 compilation of analytical data for rare-earth elements, scandium, yttrium, zirconium and hafnium in twenty-six GSJ reference samples

Abstract: Analytical data for fourteen rare-earth elements, scandium, yttrium, zirconium and hafnium, received by May 1992, have been compiled on twenty-six GSJ (Geological Survey of Japan) reference samples. Seventeen of them are 'Igneous rock series' and nine are "Sedimentary rock series". The reported data including personal communication were evaluated under the consideration on analytical methods and geochemical evidences. No significant difference has been observed between the values obtained by the different analytical methods. Based on the selected available data, 1992 compilation values were tabulated.     

Oxygen-isotope systematics of a strongly recrystallized granitic rock complex,Grenvillian Belt,SW Sweden

In the eastern, external part of the Grenvillian Belt in SW Sweden, five formations of granitic rocks were found in the basement of the Dalslandian Supracrustal Group. The granitic rocks have been strongly recrystallized but have preserved most of their granitic texture in the process. Most magmatic crystals have been pseudomorphed by metamorphic minerals: quartz, albite, chlorite, biotite, white mica, epidote, titanite, hematite, pyrite and carbonate. Two of the formations have subsequently been affected by a cataclastic deformation and at present consist of mylogneisses. ¹⁸O whole-rock values for the granitic rocks vary from +3.0 to +11.1. Quartz-apatite, quartz-zircon and quartz-titanite pairs show ¹⁸O/¹⁶O fractionations corresponding to equilibrium temperatures of 550–700° C, which are believed to reflect in the main continued closed-system isotopic exchange at high temperatures following solidification. In contrast highly positive ¹⁸O/¹⁶O fractionations for quartz-K-feldspar, quartz-biotite, quartz-chlorite and quartz-sericite pairs in some granitic samples indicate that these rocks have exchanged oxygen with heated, meteoric, H₂O dominated fluids. Other granitic samples, however, show virtually undisturbed magmatic ¹⁸O/¹⁶O fractionation values for the same mineral pairs, even though these rocks are equally altered.It is concluded that all granitic rock units recrystallized under greenschist facies conditions during the infiltration of fluids under the influence of hydrothermal convection systems set up by the intrusion of the granitic plutons. The fluids probably had a range of ¹⁸O values from ca. -14 to ca. +10, indicating the mixing of distinct fluid reservoirs, one of meteoric origin and the others of magmatic and/or metamorphic origin. The temperature of alteration is estimated at 450–500° C.Estimation of pre-alteration ¹⁸O whole rock values for the five granitic units suggests that three units should be assigned a dominantly S-type origin, where as the other two units may partly or wholly have an I-type origin.