Oxygen,sulfur, and strontium isotope and fluid inclusion studies of barite deposits from the Iglesiente-Sulcis mining district,Southwestern Sardinia,Italy

This paper deals with barite from stratiform, karst, and vein deposits hosted within Lower Paleozoic rocks of the Iglesiente-Sulcis mining district in southwestern Sardinia. For comparison sulfates from mine waters are studied. Stratiform barite displays ³⁴S=28.8–32.1, ¹⁸O=12.7–15.6, and ⁸⁷Sr/⁸⁶Sr=0.7087, in keeping with an essentially Cambrian marine origin of both sulfate and strontium. Epigenetic barite from post-Hercynian karst and vein deposits is indistinguishable for both sulfur and oxygen isotopes with ³⁴S=15.3–26.4 and ¹⁸O=6.6–12.5; ⁸⁷Sr/⁸⁶Sr ratios vary 0.7094–0.7140. These results and the microthermometric and salinity data from fluid inclusions concur in suggesting that barite formed at the site of mineralization by oxidation of reduced sulfur from Cambrian-Ordovician sulfide ores in warm, sometimes hot solutions consisting of dilute water and saline brine with different ¹⁸O values. The relative proportion of the two types of water may have largely varied within a given deposit during the mineralization. In the karst barite Sr was essentially provided by carbonate host rocks, whereas both carbonate and Lower Paleozoic shale host rocks should have been important sources for Sr of the vein barite. Finally, ³⁴S data of dissolved sulfate provide further support for the mixed seawater-meteoric water composition of mine waters from the Iglesiente area.     

Petrology and geochemistry of basalts from the American-Antarctic Ridge,Southern Ocean: implications for the westward influence of the Bouvet mantle plume

Ridge segments and fracture zones from the American-Antarctic Ridge have been systematically dredge sampled from 4° W to 18° W. Petrographic studies of the dredged basalts show that the dominant basalt variety is olivine-plagioclase basalt, although olivine-plagioclase-clinopyroxene basalt is relatively common at some localities. Selected samples have been analysed for major and trace elements, rare earth elements and Sr and Nd isotopes. These data show that the majority of samples are slightly evolved (Mg#=69-35) N-type MORB, although a small group of samples from a number of localities have enriched geochemical characteristics (T- and P-type MORB).These different types of MORB are readily distinguished in terms of their incompatible trace element and isotopic characteristics: N-type MORB have high Zr/Nb (17–78), Y/Nb (4.6–23) and ¹⁴³Nd/¹⁴⁴Nd (0.51303–0.51308) ratios, low Zr/Y (2.2–4.2) and ⁸⁷Sr/⁸⁶Sr (0.70263–0.70295) ratios and have (La/Sm)_N<1.0; T-type MORB have lower than chondritic Zr/Nb ratios (8.8–15.5), relatively low Y/Nb (1.9–4.3) and ¹⁴³Nd/¹⁴⁴Nd (0.51296–0.51288) ratios and relatively high Zr/Y (3.1–4.7), ⁸⁷Sr/⁸⁶Sr (0.70307–0.70334) and (La/Sm)_N (1.1–1.5) ratios; the single sample of P-type MORB has low Zr/Nb (6.3), Y/Nb (0.9) and ¹⁴³Nd/¹⁴⁴Nd (0.51287) ratios and high Zr/Y (7.1), ⁸⁷Sr/⁸⁶Sr (0.70351) and (La/Sm)_N (2.4) ratios. The geochemical characteristics of this sample are essentially identical to those of the Bouvet Island lavas.Geochemically enriched MORB are less abundant on the American-Antarctic Ridge than on the Southwest Indian Ridge but their geochemical characteristics are identical. The compositions of T- and P-type MORB are consistent with a regional mixing model involving normal depleted mantle and Bouvet plume type magma. On a local scale the composition of T-type MORB is consistent with derivation from depleted mantle which contains 4% veins of P-type melt.We propose a model for the evolution of the American-Antarctic Ridge lavas in which N-type MORB is derived from mantle with negligible to low vein/mantle ratios, T-type MORB is derived from domains with moderate and variable vein/mantle ratios and P-type MORB from regions with very high vein/mantle ratios where vein material comprises the major portion of the melt. The sparse occurrence of enriched lavas and by implication enriched mantle beneath the American-Antarctic Ridge, some distance (500–1,200 km) from the Bouvet plume location, is interpreted to be the result of lateral dispersion of enriched mantle domains by asthenospheric flow away from the Bouvet mantle plume towards the American-Antarctic Ridge.     

Stable and Sr-isotope evidence for fluid advection during thrusting of the glarus nappe (swiss alps)

At the Glarus thrust in the Swiss Helvetic Alps, Permian Verrucano siltstones are allochthonously superimposed over Tertiary Flysch with an intermediate, about 1 metre thin layer of intensively deformed calcmylonite of probable Mesozoic provenance. The H–O–C- and Sr-isotope compositions of minerals from the calc-mylonite and strongly mylonitized Verrucano siltstones were determined in order to assess: (1) equilibrium-disequilibrium relationships; (2) isotopic composition of the fluid phase, its provenance and water/rock ratios; (3) sources of Sr in the calc-mylonite; (4) deformation temperatures. The isotopic composition of cale-mylonite micro-samples from five sites along the thrust varies from 22 to 12 and 2 to-10 for ¹⁸O and ¹³C respectively. All samples are ¹⁸O depleted by up to 14 relative to the presumed marine Helvetic carbonate protoliths (¹⁸O=25.4±2). A pronounced geographic trend of ¹⁸O depletion from 22 in the north to 12 in the south is observed. In calc-mylonites, ⁸⁷Sr/⁸⁶Sr ratios range from typical Mesozoic marine carbonate protolith signatures (0.708±0.005) to more radiogenic values as high as 0.722. A variable contribution of radiogenic ⁸⁷Sr to the calc-mylonite is though to reflect interaction with fluids that aquired their Sr from the Hercynian granitic basement. Chlorites and muscovites from the calc-mylonite and Verrucano have uniform ¹⁸O values but display D values from-40 to-147%: the D-enriched values correspond to the primary metamorphic or formational fluids expelled during thrusting, whereas the D-depleted samples reflect selective H-isotope exchange with meteoric fluids during uplift of the Alpine belt. The isotopic composition of the calc-mylonites requires exchange with ¹⁸O—depleted, ⁸⁷Sr—enriched fluids at very high water/rock ratios. Possible sources for these are dewatering of the underlying Flysch and/or metamorphic fluids, or formation brines expelled along the thrust from greater depth. These could be derived from compaction and dewatering of the Flysch in the northern part of the thrust; in the south, however, where Verrucano is thrust over ¹⁸O-rich Mesozoic carbonates, the extreme ¹⁸O depletion of the calc-mylonite has to be explained either by fluid advection within the Verrucano hanging wall and thrust zone or alternatively by exchange with metamorphic fluids from greater depth, expelled along the thrust. Microstructural evidence (abundant veins, stylolites, breccias) suggests that fluids played an important role in deformation and strain localization. Excepting albite all major components (quartz, chlorite, muscovite, calcite) are both dynamically recrystallized and crystallized as secondary minerals in pressure shadows and syn-mylonitic veins, indicating that these minerals were potentially open to oxygen isotopic exchange during alpine metamorphism and thrust deformation. Within the mylonitized Verrucano silstones, isolated quartz-chlorite and quartz-calcite fractionations yield temperatures of around 320°C close to values obtained from calcite-dolomite thermometry (355°C±30) and in agreement with the regional lower greenschist facies metamorphism. Quartz-calcite and quartz-albite fractionations indicate slightly lower temperatures around 250°C, owing to selective lower temperature re-equilibration of the calcite and albite during post peak metamorphism.     

Nd and Sr isotope systematics of the Oka complex,Quebec, and their bearing on the evolution of the sub-continental upper mantle

A detailed isotopic study of minerals and whole rocks from the Cretaceous Oka complex, Quebec, Canada, shows a very small variation in initial Nd and Sr isotopic compositions. Assuming an age of 109 Ma for the complex, apatite, calcite, garnet, melilite, monticellite, olivine and pyroxene and whole rocks yield a range for initial ⁸⁷Sr/⁸⁶Sr of 0.70323–0.70333; and for initial ¹⁴³Nd/¹⁴⁴Nd of 0.51271–0.51284 ( _SR(T)= –14.8 to –16.2; _Nd(T)=+4.1 to +6.6). The negative _SR and positive _Nd indicate derivation of the Nd and Sr from a source with a time-integrated depletion in the large-ion lithophile (LIL) elements. This agrees with data from other Canadian carbonatites and confirms that a large part of the Canadian Shield is underlain by a source region depleted in the LIL elements. The new data from Oka suggest that the depleted source may have remained coupled to the continental crust until recent time.     

Strontium isotopic and selected trace element variations between two Aleutian volcanic centers (Adak and Atka): implications for the development of arc volcanic plumbing systems

Major and trace element concentrations and initial ⁸⁷Sr/⁸⁶Sr ratios of lavas from the Aleutian volcanic centers of Adak and Atka have been used to study the evolution of their respective lithospheric plumbing systems. The centers are within 150 km of one another and show similar overall silica ranges (47–67%), but Adak (40 km³) is smaller than Atka (200 km³). Adak's lavas are chemically and isotopically heterogeneous (⁸⁷Sr/⁸⁶Sr:0.70285–0.70330) and two units contain lithospheric xenoliths. The lavas of the much larger Atka, on the other hand, have much less variability in major and trace elements as well as ⁸⁷Sr/⁸⁶Sr (0.70320–0.70345). We suggest that these characteristics are a measure of the relative maturity and cleanliness of the lithospheric plumbing systems that supply magma to these centers. Because Aleutian volcanic centers often remain fixed for relatively long periods of time (5 m.y.), once established, magmatic passageways are repeatedly used. Young plumbing systems are relatively cool and contain large amounts of wallrock contaminant, and ascending magmas undergo contamination as well as concurrent crystallization and fractionation. With time, however, heat and mass transfer between ascending magmas and wallrock produce thermal and chemical boundary layers that insulate subsequent magmas. In effect, the plumbing system matures. The chemical heterogeneity displayed by young, dirty systems (like Adak) reflects not only the magma source but also the wallrock encountered during ascent and possibly the effects of extensive crystal fractionation. Thus, it is the petrologic data of mature, clean systems, like Atka, that yield the most direct and unambiguous information on the ultimate origin of the lavas and their near surface evolution.     

Mixing of magmas from enriched and depleted mantle sources in the northeast Pacific: West Valley segment,Juan de Fuca Ridge

The 50 km-long West Valley segment of the northern Juan de Fuca Ridge is a young, extension-dominated spreading centre, with volcanic activity concentrated in its southern half. A suite of basalts dredged from the West Valley floor, the adjacent Heck Seamount chain, and a small near-axis cone here named Southwest Seamount, includes a spectrum of geochemical compositions ranging from highly depleted normal (N-) MORB to enriched (E-) MORB. Heck Seamount lavas have chondrite-normalized La/Sm_cn0.3, ⁸⁷Sr/⁸⁶Sr=0.70235–0.70242, and ²⁰⁶Pb/²⁰⁴Pb=18.22–18.44, requiring a source which is highly depleted in trace elements both at the time of melt generation and over geologic time. The E-MORB from Southwest Seamount have La/Sm_cn1.8, ⁸⁷Sr/⁸⁶Sr=0.70245–0.70260, and ²⁰⁶Pb/²⁰⁴Pb=18.73–19.15, indicating a more enriched source. Basalts from the West Valley floor have chemical compositions intermediate between these two end-members. As a group, West Valley basalts from a two-component mixing array in element-element and element-isotope plots which is best explained by magma mixing. Evidence for crustal-level magma mixing in some basalts includes mineral-melt chemical and isotopic disequilibrium, but mixing of melts at depth (within the mantle) may also occur. The mantle beneath the northern Juan de Fuca Ridge is modelled as a plum-pudding, with plums of enriched, amphibole-bearing peridotite floating in a depleted matrix (DM). Low degrees of melting preferentially melt the plums, initially removing only the amphibole component and producing alkaline to transitional E-MORB. Higher degrees of melting tap both the plums and the depleted matrix to yield N-MORB. The subtly different isotopic compositions of the E-MORBs compared to the N-MORBs require that any enriched component in the upper mantle was derived from a depleted source. If the enriched component crystallized from fluids with a DM source, the plums could evolve to their more evolved isotopic composition after a period of 1.5–2.0 Ga. Alternatively, the enriched component could have formed recently from fluids with a less-depleted source than DM, such as subducted oceanic crust. A third possibility is that enriched material might be dispersed as plums throughout the upper mantle, transported from depth by mantle plumes.     

Nd-Sr isotopic and trace element study of rocks and fluids from the continental deep drilling Project (KTB), Germany

Geochemical analyses were interpreted on the dominant lithological units and on a deep crustal fluid from the Continental Deep Drilling Project (KTB) Pilot Hole, situated at the western margin of the Variscan Bohemian Massif. The biotite gneiss (from 384 m depth) shows a rare earth element pattern very similar to the European shale composite with Nd model ages of 940 Ma (CHUR) and 1.4 Ga (DM). The lamprophyre dike in the upper profile (1549 m), a nepheline and olivine normative basalt, is geochemically and isotopically similar to rocks from the Tertiary Central European Volcanic Province. The lower metabasite sequence (3575–4000 m), with an intrusion age of approximately 500 Ma, is made up primarily of highly metamorphosed subalkalic olivine basalts. The geochemical characteristics of the metabasites are a (La/Yb)_N of 5–10, an La concentration of 20–50 times chondrite as well as (⁸⁷Sr/⁸⁶Sr)_i of 0.7035–0.7038 and _Nd(T) of 4–6. These values suggest a depleted mantle source for the igneous precursors, evolving by assimilation-fractional crystallization processes with up to 25% of upper crust into the ultramafic, basaltic, and intermediate rock types of the metabasite sequence. The strong geochemical and chronological similarities between the KTB metabasites and rocks from the Münchberg Massif suggest that these units belong to the same lithological complex. The high salinity as well as the radiogenic ⁸⁷Sr/⁸⁶Sr ratio of 0.709413 in the KTB fluid from 4000 m depth might be the result of migrating fluids reacting with the regional Permo-Mesozoic evaporite deposits, followed by extensive Sr isotopic exchange with the upper crust.     

Sr, C and O isotope systematics in the Pucará basin, central Peru

A combined Sr, O and C isotope study has been carried out in the Pucará basin, central Peru, to compare local isotopic trends of the San Vicente and Shalipayco Zn-Pb Mississippi Valley-type (MVT) deposits with regional geochemical patterns of the sedimentary host basin. Gypsum, limestone and regional replacement dolomite yield ⁸⁷Sr/⁸⁶Sr ratios that fall within or slightly below the published range of seawater ⁸⁷Sr/⁸⁶Sr values for the Lower Jurassic and the Upper Triassic. Our data indicate that the Sr isotopic composition of seawater between the Hettangian and the Toarcian may extend to lower ⁸⁷Sr/⁸⁶Sr ratios than previously published values. An ⁸⁷Sr-enrichment is noted in (1) carbonate rocks from the lowermost part of the Pucará basin, and (2) different carbonate generations at the MVT deposits. This indicates that host rocks at MVT deposits and in the lower-most part of the carbonate sequence interacted with ⁸⁷Srenriched fluids. The fluids acquired their radiogenic nature by interaction with lithologies underlying the carbonate rocks of the Pucará basin. The San Ramón granite, similar Permo-Triassic intrusions and their clastic derivatives in the Mitu Group are likely sources of radiogenic ⁸⁷Sr. The Brazilian shield and its erosion products are an additional potential source of radiogenic ⁸⁷Sr. Volcanic rocks of the Mitu Group are not a significant source for radiogenic ⁸⁷Sr; however, molasse-type sedimentary rocks and volcaniclastic rocks cannot be ruled out as a possible source of radiogenic ⁸⁷Sr. The marked enrichment in ⁸⁷Sr of carbonates toward the lower part of the Pucará Group is accompanied by only a slight decrease in ¹⁸O values and essentially no change in ¹³C values, whereas replacement dolomite and sparry carbonates at the MVT deposits display a coherent trend of progressive ⁸⁷Sr-enrichment, and ¹⁸O- and ¹³C-depletion. The depletion in ¹⁸O in carbonates from the MVT deposits are likely related to a temperature increase, possibly coupled with a ¹⁸O-enrichment of the ore-forming fluids. Progressively lower ¹³C values throughout the paragenetic sequence at the MVT deposits are interpreted as a gradually more important contribution from organically derived carbon. Quantitative calculations show that a single fluid-rock interaction model satisfactorily reproduces the marked ⁸⁷Sr-enrichment and the slight decrease in ¹⁸O values in carbonate rocks from the lower part of the Pucará Group. By contrast, the isotopic covariation trends of the MVT deposits are better reproduced by a model combining fluid mixing and fluid-rock interaction. The modelled ore-bearing fluids have a range of compositions between a hot, saline, radiogenic brine that had interacted with lithologies underlying the Pucará sequence and cooler, dilute brines possibly representing local fluids within the Pucará sequence. The composition of the local fluids varies according to the nature of the lithologies present in the neighborhood of the different MVT deposits. The proportion of the radiogenic fluid in the modelled fluid mixtures interacting with the carbonate host rocks at the MVT deposits decreases as one moves up in the stratigraphic sequence of the Pucará Group.     

Nd,Sr, and O isotopic variations in metaluminous ash-flow tuffs and related volcanic rocks at the Timber Mountain/Oasis Valley Caldera,Complex, SW Nevada: implications for the origin and evolution of large-volume silicic magma bodies

Nd, Sr and O isotopic data were obtained from silicic ash-flow tuffs and lavas at the Tertiary age (16–9 Ma) Timber (Mountain/Oasis Valley volcanic center (TMOV) in southern Nevada, to assess models for the origin and evolution of the large-volume silicic magma bodies generated in this region. The large-volume (>900 km³), chemically-zoned, Topopah Spring (TS) and Tiva Canyon (TC) members of the Paintbrush Tuff, and the Rainier Mesa (RM) and Ammonia Tanks (AT) members of the younger Timber Mountain Tuff all have internal Nd and Sr isotopic zonations. In each tuff, high-silica rhyolites have lower initial _Nd values (1 _Nd unit), higher⁸⁷Sr/⁸⁶Sr, and lower Nd and Sr contents, than cocrupted trachytes. The TS, TC, and RM members have similar _Nd values for high-silica rhyolites (-11.7 to -11.2) and trachytes (-10.5 to -10.7), but the younger AT member has a higher _Nd for both compositional types (-10.3 and -9.4). Oxygen isotope data confirm that the TC and AT members were derived from low _Nd magmas. The internal Sr and Nd isotopic variations in each tuff are interpreted to be the result of the incorporation of 20–40% (by mass) wall-rock into magmas that were injected into the upper crust. The low _Nd magmas most likely formed via the incorporation of low ¹⁸O, hydrothermally-altered, wall-rock. Small-volume rhyolite lavas and ash-flow tuffs have similar isotopic characteristics to the large-volume ash-flow tuffs, but lavas erupted from extracaldera vents may have interacted with higher ¹⁸O crustal rocks peripheral to the main magma chamber(s). Andesitic lavas from the 13–14 Ma Wahmonie/Salyer volcanic center southeast of the TMOV have low _Nd (-13.2 to -13.8) and are considered on the basis of textural evidence to be mixtures of basaltic composition magmas and large proportions (70–80%) of anatectic crustal melts. A similar process may have occurred early in the magmatic history of the TMOV. The large-volume rhyolites may represent a mature stage of magmatism after repeated injection of basaltic magmas, crustal melting, and volcanism cleared sufficient space in the upper crust for large magma bodies to accumulate and differentiate. The TMOV rhyolites and 0–10 Ma old basalts that erupted in southern Nevada all have similar Nd and Sr isotopic compositions, which suggests that silicic and mafic magmatism at the TMOV were genetically related. The distinctive isotopic compositions of the AT member may reflect temporal changes in the isotopic compositions of basaltic magmas entering the upper crust, possibly as a result of increasing basification of a lower crustal magma source by repeated injection of mantle-derived mafic magmas.     

Major and trace element geochemistry in upper Ganga river in the Himalayas, India

Chemical weathering and resulting water compositions in the upper Ganga river in the Himalayas were studied. For the first time, temporal and spatial sampling for a 1 year period (monthly intervals) was carried out and analyzed for dissolved major elements, trace elements, Rare Earth Elements (REE), and strontium isotopic compositions. Amounts of physical and chemical loads show large seasonal variations and the overall physical load dominates over chemical load by a factor of more than three. The dominant physical weathering is also reflected in high quartz and illite/mica contents in suspended sediments. Large seasonal variations also occur in major elemental concentrations. The water type is categorized as HCO₃^––SO₄^2––Ca²⁺ dominant, which constitute >60% of the total water composition. On an average, only about 5–12% of HCO₃^– is derived from silicate lithology, indicating the predominance of carbonate lithology in water chemistry in the head waters of the Ganga river. More than 80% Na⁺ and K⁺ are derived from silicate lithology. The silicate lithology is responsible for the release of low Sr with extremely radiogenic Sr (⁸⁷Sr/⁸⁶ Sr>0.75) in Bhagirathi at Devprayag. However, there is evidence for other end-member lithologies for Sr other than carbonate and silicate lithology. Trace elements concentrations do not indicate any pollution, although presence of arsenic could be a cause for concern. High uranium mobilization from silicate rocks is also observed. The REE is much less compared to other major world rivers such as the Amazon, perhaps because in the present study, only samples filtered through <0.2 m were analysed. Negative Eu anomalies in suspended sediments is due to the excess carbonate rock weathering in the source area.     

Low δ18O silicic volcanic rocks at the Calabozos caldera complex,southern Andes

Sr- and Pb-isotope data from the Calabozos center (⁸⁷Sr/⁸⁶Sr= 0.7043, ²⁰⁶Pb/²⁰⁴Pb=18.64–18.66, ²⁰⁷Pb/²⁰⁴Pb=15.59–15.60, ²⁰⁸Pb/²⁰⁴Pb=38.52–38.55) fall within the range of values reported for the southern volcanic zone (33–42° S) of the Andean arc. The range of ¹⁸O (5.0–6.3), however, includes unusually low values compared to volcanic rocks of similar bulk composition in the region. The Calabozos caldera complex lies at 35 °30 S, where the continental crust under the Andes thins southward from >45 to 30 km. Three voluminous late Pleistocene ashflow tuffs, collectively called the Loma Seca Tuff, constitute the bulk of >1,000 km³ of eruptive products at the Calabozos caldera complex and are evidence for a major, longlived andesitic-to-rhyodacitic magma reservoir at shallow crustal levels. The ¹⁸O values of the most evolved volcanic rocks from the Calabozos center are lower than predicted for rhyodacite produced by crystal fractionation from basalt typical of the region. Variation of ¹⁸O independent of bulk composition and inferred magmatic water contents indicates that the ¹⁸O depletion is a late-stage, upper-crustal phenomenon that cannot simply be attributed to magmatic interaction with meteoric water. The data are interpreted to be the result of assimilation of 5–30% of roof and wall rocks previously depleted in ¹⁸O by isotopic exchange in a meteoric hydrothermal system overlying the magma reservoir. Combined assimilation and fractional crystallization calculations applied to Sr isotope data show that the isotopic contrast between the Calabozos magmas and the assimilated rocks is very small. Hydrothermally-altered volcanic and plutonic rocks from the Tertiary Andean arc complex and Mesozoic-to-Cenozoic volcaniclastic sediments typical of the local basement provide a geologically reasonable contaminant compatible with the Sr- and O-isotope data. Pb-isotope data from the Calabozos system lend no significant insight into upper crustal contamination.     

Fluid flow in subduction zones: evidence from Nd- and Sr-isotope variations in metabasalts of the Franciscan complex,California

Greenstone, blueschist and eclogite metabasaltic blocks from the Franciscan complex of California preserve extensive petrographic and chemical evidence for interaction with hydrous fluids at high-P, low-T metamorphic conditions. The Nd and Sr isotope variations within and among the blocks constrain the origin of the basaltic protoliths, the nature of the fluid metasomatism that occurred within the upper levels (15–45 km) of the paleosubduction zonc, and the character and provenance of the rock that generated the hydrous fluids within the paleosubduction zone. Samples with little or no petrographic evidence of retrograde alteration and unaltered garnet separates have _Nd. With increasing degrees of retrograde alteration, Nd isotope compositions are consistently lower, ranging down to _Nd(160)=5. Actinolitic alteration rinds which are present on some blocks have the least radiogenic compositions with _Nd=1.6 to 6.1. While Nd isotope compositions of unaltered blockes are in the range expected for basalt derived from normal depleted mantle, the Sr isotope compositions are more radiogenic ranging from _Sr(160)=–5 to +11. Compositions of unaltered eclogite and blue-schist blocks are consistent with a protolith origin in normal oceanic crust derived from depleted mantle. The Sr isotopy systematics indicate that the protoliths were modified by seawater alteration in an ocean-floor hydrothermal system. Isotopic compositions of samples from parts of blocks that have a retrograde metamorphic overprint show a strong correlation between less radiogenic Nd compositions and the extent of retrograde metamorphism. Maximum Nd isotope ratios of the metasomatizing fluid are provided by analyses of actinolitic rinds, and range from _Nd(160)=1.6 to 6.1. A possible source for fluids of this composition is subducted sediment that was derived from a continental craton. Because rind formation occurred while the basaltic blocks were within an ultramafic matrix, the fluids must have migrated from sediments in the accretionary wedge into an overlying wedge of mantle material imbricated with blocks of oceanic crust. This suggests possibly km-scale movement of fluids that carry an amount of the rare-earth elements sufficient to significantly modify the trace-element budget of subducted basalt.     

The role of hydrogen bonding in the thermal expansion and dehydration of brushite,di-calcium phosphate dihydrate

The unit-cell and atomic parameters of perdeuterated brushite have been extracted from Rietveld analysis of neutron powder diffraction data within the temperature range 4.2 to 470 K. The thermal expansion of brushite is anisotropic, with the largest expansion along the b axis due principally to the effect of the O(1)···D(4) and O(3)···D(2) hydrogen bonds. Expansion along the c axis, influenced by the Ow1···D(5) interwater hydrogen bond, is also large. The high temperature limits for the expansion coefficients for the unit-cell edges a, b and c are 9.7(5) × 10^–6, 3.82(9) × 10^–5 and 5.54(5) × 10^–5 K^–1, respectively, and for the cell volume it is 9.7(1) × 10^–5 K^–1. The angle displays oscillatory variation, and empirical data analysis results in = 1.28(3) × 10^–6sin(0.0105 T) K^–1, within this temperature range. The evolution of the thermal expansion tensor of brushite has been calculated between 50 T 400 K. At 300 K the magnitudes of the principal axes are ₁₁ = 50(6) × 10^{–6 K–1}, ₂₂ = 26.7(7) × 10^–6 K^–1 and ₃₃ = 7.0(5) × 10^–6 K^–1. The intermediate axis, ₂₂, is parallel to b, and using IRE convention for the tensor orthonormal basis, the axes ₁₁ and ₃₃ have directions equal to (–0.228, 0, –0.974) and (–0.974, 0, 0.228) respectively. Under the conditions of these experiments, the onset of dehydration occurred at temperatures above 400 K. Bond valence analysis combined with assessments of the thermal evolution of the bonding within brushite suggests that dehydration is precipitated through instabilities in the chemical environment of the second water molecule.     

Isotopic Composition (δ13C, δ18O) and Origin of Manganese Carbonate Ores of the Usa Deposit (Kuznetskii Alatau)

Isotopic compositions of carbon and oxygen are studied in different (rhodochrosite, calcareous-rhodochrosite, and chlorite–rhodochrosite) types of manganese carbonate ores from the Usa deposit (Kuznetskii Alatau). The ¹³C value varies from –18.4 to –0.7, while the ¹⁸O value ranges between 18.4 and 23.0. Host rocks are characterized by higher values of ¹³C (–1.9 to 1.0) and ¹⁸O (21.2 to 24.3). The obtained isotope data suggest an active participation of oxidized organic carbon in the formation of manganese carbonates. Manganese carbonate ores of the deposit are probably related to metasomatic processes.     

Petrology and geochemistry of Rodrigues Island,Indian Ocean

Rodrigues Island is composed of a differentiated series of transitional-mildly alkaline olivine basalts. The lavas contain phenocrysts of olivine (Fo_88–68)±plagioclase (An_73–50), together with a megacryst suite involving olivine, plagioclase, kaersutite, clinopyroxene, apatite, magnetite and hercynite-rich spinels. Troctolitic-anorthositic gabbro xenoliths are widely dispersed throughout the lavas and are probably derived from the upper parts of an underlying layered complex: the megacrysts may originate from coarse, easily disaggregated differentiates near the top of this body.Modelling of major and trace element data suggests that the majority of chemical variation in the lavas results from up to 45% fractionation of olivine, clinopyroxene, plagioclase and magnetite at low pressures, in the ratio 2035396. The clinopyroxene-rich nature of this extract assemblage is significantly different to that of the xenoliths, and suggests that clinopyroxene-rich gabbros and/or ultrabasic rocks may lie at greater depth.Sr and Nd isotopic data (⁸⁷Sr/⁸⁶Sr 0.70357–070406,¹⁴³Nd/¹⁴⁴Nd 0.51283–0.51289) indicate a mantle source with relative LREE depletion, and emphasise an unusual degree of uniformity in Indian Ocean island sources. A small group of lavas with strong HREE enrichment suggest a garnet-poor source for these, while high overall Al₂O₃/ CaO ratios imply high clinopyroxene/garnet ratios in refractory residua.     

Formation of Mud-Volcanic Fluids in Taman (Russia) and Kakhetia (Georgia): Evidence from Boron Isotopes

Temperatures of the formation of mud-volcanic waters are determined based on concentrations of some temperature-dependent components (Na–Li, Mg–Li). Estimates obtained for the Taman and Kakhetia regions are similar and range from 45 to 170°, which correspond to depths of 1–4.5 km. The calculated temperatures correlate with the chemical (Li, Rb, Cs, Sr, Ba, B, I, and HCO₃) composition of water and ¹³ (₂) and ¹³ (CH₄) values in spontaneous gases. The isotope values indicate that mechanisms of the formation of ¹³-rich gases, i.e., gases with high ¹³ values (up to +16.0 in ₂ and –23.4 in CH₄) in mud-volcanic systems of Taman and Kakhetia are governed by fluid-generation temperatures rather than the supply of abyssal gases. The ¹¹ value was determined for the first time in mud-volcanic products of the Caucasus region. This value ranges from +22.5 to +39.4 in the volcanic water of Georgia, from –1.2 to +7.4 in the clayey pulp of Georgia, and from –7.6 to +13.2 in the clayey pulp of Taman. It is shown that the ¹¹ value in clay correlates with the fluid-generation temperature and ¹¹ correlates with ¹³ in carbon-bearing gases. These correlations probably testify to the formation of different phases of mud-volcanic emanations in a single geochemical system and suggest the crucial role of temperature in the development of isotope-geochemical features.     

Late Archaean crust-mantle interactions: geochemistry of LREE-enriched mantle derived magmas. Example of the Closepet batholith,southern India

The Closepet batholith in South India is generally considered as a typical crustal granite emplaced 2.5 Ga ago and derived through partial melting of the surrounding Peninsular Gneisses (3.3 to 3.0 Ga). In the field, it appears as a composite batholith made up of at least two groups of intrusions. (a) An early SiO₂-poor group (clinopyroxene quartz-monzonite and porphyritic phyritic monzogranite) is located in the central part of the batholith. These rocks display a narrow range in both initial ⁸⁷Sr/⁸⁶Sr (0.7017–0.7035) and _Nd(–0.9to –4.1). (b) A later SiO₂-rich group (equigranular grey and pink granites) is located along the interface between the SiO₂-poor group and the Peninsular Gneisses. They progressively grade into migmatised Peninsular Gneisses, thus indicating their anatectic derivation. Their isotopic characteristics vary over a wide range (⁸⁷Sr/⁸⁶Sr ratios=0.7028–0.7336 and _Nd values from-2.7 to-8.3, at 2.52 Ga). Field and geochronological evidence shows that the two groups are broadly contemporaneous (2.518–2.513 Ga) and mechanically mixed. This observation is supported by the chemical data that display well defined mixing trends in the _Sr vs _Nd and elemental variation diagrams. The continuous chemical variation of the two magmatic bodies is interpreted in terms of interaction and mixing of two unrelated end-members derived from different source regions (enriched peridotitic mantle and Peninsular Gneisses). It is proposed that the intrusion of mantle-derived magmas into mid-crustal levels occurred along a transcurrent shear zone; these magmas supplied additional heat and fluids that initiated anatexis of the surrounding crust. During this event, large-scale mixing occurred between mantle and crustal melts, thus generating the composite Closepet batholith. The mantle-derived magmatism is clearly associated with granulite facies metamorphism 2.51±0.01 Ga ago. Both are interpreted as resulting from a major crustal accretion event, possibly related to mantle plume activity.     

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.     

The oxygen isotope composition of granitoid and sedimentary rocks of the southern Snake Range,Nevada

Six diverse intrusive igneous types are exposed as discrete outcrops within an area of 900 km² in the southern Snake Range, White Pine County, Nevada. The previously recognized variety among these igneous types is reflected in the wide range of ¹⁸O values (–1.1 to 13.4 permil) found in these rocks. This range of ¹⁸O values probably results from differences in source material and post-crystallization history of the different intrusive types.The Jurassic intrusive of the Snake Creek-Williams Canyon area represents the chemical equivalent of a large part of a differentiation sequence, with the entire range of composition (63–76 percent SiO₂) exposed over a horizontal distance of about five km. The rather regular increase of ¹⁸O values from the most mafic to the most felsic parts of this pluton, together with ¹⁸O values determined for constituent minerals recovered from five of the samples, supports a fractional crystallization model. The high ¹⁸O values found (10.2–12.2 permil) indicate that the magma likely was derived from or assimilated sedimentary materials.Nine samples of the Cretaceous two-mica granite of the Pole Canyon-Can Young Canyon area have ¹⁸O values in the range 10.6–12.1 permil. These high ¹⁸O values, an initial⁸⁷Sr/⁸⁶Sr ratio of 0.7165, and the presence of muscovite along with an accessory mineral suite limited to monazite, apatite, zircon, and an allanite-like mineral, characterize this intrusive mass as an S-type granite. It probably formed through anatexis of late Precambrian pelitic rocks.The granitoid rock exposed in the Young Canyon-Kious Basin area is Tertiary (32 m.y.). Most of this intrusive has been cataclastically deformed as a result of late (18 m.y.) movement on the overlying Snake Range decollement. The undeformed portion of this intrusive has ¹⁸O values of 8.7–10.0 permil. However, the deformed portion of this intrusive has ¹⁸O values as low as –1.1 permil, apparently resulting from isotopic exchange between this rock and ground water at the time of cataclasis.Although the igneous types exposed in the southern Snake Range differ petrologically and range in age from Jurassic to Tertiary, most have relatively high ¹⁸O values compared with other granitoid rocks of the Basin-Range Province.     

Defining the urban

In everyday discourse, the term urban causes few problems, but it certainly has for social theory. While the paper accepts the recent consensus that the term no longer serves to refer to a distinct object in capatalist societies, it argues that the familiar arguments have been confused by inadequate approaches to the problem of definition and inadequate concepts of space and ideology. Clarification of such definitions is a prime task of social theory and different methods of definition are discussed. The paper ends with a commentary on what is probably the best attempt at defining the urban — Raymond Williams The Country and the City.