Strontium and oxygen isotopic composition of some basalts from Hole 504B,Costa Rica Rift,DSDP Legs 69 and 70

Seventeen whole-rock samples, generally taken at 25–50 m intervals from 5 to 560 m sub-basement in Hole 504B, drilled in 6.2 m.y. old crust, were analysed for⁸⁷Sr/⁸⁶Sr ratios, Sr and Rb concentrations, and¹⁸O/¹⁶O ratios. Sr isotope ratios for 8 samples from the upper 260 m of the hole range from 0.70287 to 0.70377, with a mean of 0.70320. In the 330–560 m interval, 5 samples have a restricted range of 0.70255–0.70279, with a mean of 0.70266, the average value for fresh mid-ocean ridge basalts (MORB). In the 260–330 m interval, approximately intermediate Sr isotopic ratios are found.δ¹⁸O values (‰) range from 6.4 to 7.8 in the upper 260 m, 6.2–6.4 in the 270–320 m interval, and 5.8–6.2 in the 320–560 m interval. The values in the upper 260 m are typical for basalts which have undergone low-temperature seawater alteration, whereas the values for the 320–560 m interval correspond to MORB which have experienced essentially no oxygen isotopic alteration.The higher⁸⁷Sr/⁸⁶Sr and¹⁸O/¹⁶O ratios in the upper part of the hole can be interpreted as the result of a greater overall water/rock ratio in the upper part of the Hole 504B crust than in the lower part. Interaction of basalt with seawater(⁸⁷Sr/⁸⁶Sr=0.7091) increased basalt⁸⁷Sr/⁸⁶Sr ratios and produced smectitic alteration products which raised whole-rock δ¹⁸O values. Seawater circulation in the lower basalts may have been partly restricted by the greater number of relatively impermeable massive lava flows below about 230 m sub-basement. These flows may have helped to seal off lower basalts from through-flowing seawater.     

Mineralogy and stable isotope geochemistry of hydrothermally altered oceanic rocks

Data for the diffusion of cations in pyroxenes are relevant to a variety of sub-solidus processes including order-disorder and exsolution. Similar data must also be available if the reliability of geobarometers and geothermometers involving pyroxenes is to be assessed. Two types of diffusion experiment have been performed to determine cation diffusion rates in pyroxenes: (1) interdiffusion between single crystals of diopside and polycrystalline sinters enriched in Al and Fe, and (2) interdiffusion between single crystals of diopside and a glass of the same composition which was isotopically enriched in²⁶Mg and⁴³Ca. Following high-temperature annealing for periods up to several hundred hours, analysis of the diffusion couples, using an electron microprobe and an ion microprobe respectively, failed to show any measurable diffusion profiles. From these “null result” experiments the diffusion coefficients (D) for Al and Fe in diopside are estimated to be less than4×10^?14cm²s^?1 at 1200°C, and values ofD for Ca and Mg in diopside are estimated to be less than7 × 10^?14cm²s^?1 at 1250°C. These rates are significantly slower than published tracer-type diffusion data for Ca and Al.A review of studies of order-disorder, microstructural coarsening, and diffusion in pyroxenes suggest that activation energies for cation exchange are typically in excess of 60 kcal mol^?1. Transport rates will be assisted, and activation energies lowered by sample non-stoichiometry, inhomogeneities, high dislocation densities and the presence of water.The collective data for Al, Mg and Ca diffusion in diopside indicate diffusion coefficients? 10^?15cm²s^?1 at 1200°C. A comparison with data for diffusion in garnet, olivine and spinel suggests that pyroxenes may have the highest blocking temperatures.     

An oxygen isotopic profile through the upper kilometer of the oceanic crust, DSDP Hole 504B

DSDP Hole 504B is the deepest basement hole in the oceanic crust, penetrating through a 571.5 m pillow section, a 209 m lithologic transition zone, and 295 m into a sheeted dike complex. An oxygen isotopic profile through the upper crust at Site 504 is similar to that in many ophiolite complexes, where the extrusive section is enriched in¹⁸O relative to unaltered basalts, and the dike section is variably depleted and enriched. Basalts in the pillow section at Site 504 haveδ¹⁸O values generally ranging from +6.1 to +8.5‰ SMOW(mean= +7.0‰), although minor zeolite-rich samples range up to 12.7‰. Rocks depleted in¹⁸O appear abruptly at 624 m sub-basement in the lithologic transition from 100% pillows to 100% dikes, coinciding with the appearance of greenschist facies minerals in the rocks. Whole-rock values range to as low as +3.6‰, but the mean values for the lithologic transition zone and dike section are +5.8 and +5.4‰, respectively.

Oxygen and carbon isotopic data for secondary vein minerals combined with the whole rock data provide evidence for the former presence of two distinct circulation systems separated by a relatively sharp boundary at the top of the lithologic transition zone. The pillow section reacted with seawater at low temperatures (near 0°C up to a maximum of around 150°C) and relatively high water/rock mass ratios (10–100); water/rock ratios were greater and conditions were more oxidizing during submarine weathering of the uppermost 320 m than deeper in the pillow section. The transition zone and dikes were altered at much higher temperatures (up to about 350°C) and generally low water/rock mass ratios ( 1), and hydrothermal fluids probably contained mantle-derived CO₂. Mixing of axial hydrothermal fluids upwelling through the dike section with cooler seawater circulating in the overlying pillow section resulted in a steep temperature gradient ( 2.5°C/m) across a 70 m interval at the top of the lithologic transition zone. Progressive reaction during axial hydrothermal metamorphism and later off-axis alteration led to the formation of albite- and Ca-zeolite-rich alteration halos around fractures. This enhanced the effects of cooling and¹⁸O enrichment of fluids, resulting in local increases inδ¹⁸O of rocks which had been previously depleted in¹⁸O during prior axial metamorphism.     

Strontium isotope composition of ophiolitic and related rocks,Drocea Mountains,Rumania

Strontium isotopic analyses are reported for ophiolitic and associated rocks of Mesozoic and Tertiary age from the Drocea Mountains. The samples and their average Sr⁸⁷/Sr⁸⁶ and Rb/Sr ratios, in order, include: (a) ultramafics (partly serpentinized or uralitized peridotite, peridotite-melagabbro). 0.7043, 0.106; (b) gabbros, dolerites and anemasites (including magnetite-bearing, quartz dolerite, hornblende and normal gabbros), 0.7032, 0.021; (c) basalts (amygdaloidal, hyalopyroclasite), 0.7030, 0.040; and (d) granophyric and albitic vein rocks, 0.7046, 0.058. Also analyzed were (e) basalt-spilites of a younger intrusive cycle 0.7042, 0.046 (f) banatites, 0.7064, 0.542. Two Quaternary volcanics were analyzed from outside the Drocea Mountains: (g) augite-hypersthene andesite from Mt. Gut?i, 0.7083, 0.247, and olivine basalt from Raco?, 0.7043, 0.056. The data for the ophiolite suite show highest Sr⁸⁷/Sr⁸⁶ and Rb/Sr ratios in the ultramafics which suggests a two-stage origin with the ultramafics derived from a more primitive mantle than the later gabbros and basalts. Initial Sr⁸⁷/Sr⁸⁶ ratios range from 0.7021 to 0.7045 in gabbro and basalt and 0.7035 to 0.7056 in peridotite which is well within the limits found in oceanic tholeiites and suggests an origin for the complex as a spreading oceanic ridge. Cross-cutting felsic granophyric and albititic rocks as well as the late-stage basalts (a) have relatively low Sr⁸⁷/Sr⁸⁶ and Rb/Sr ratios, (b) represent a small volume, and (c) are intimately related to the ophiolites. They appear to have developed largely by late-stage differentiation and fractional crystallization of a tholeiitic magma. The higher ratios for the banatites and andesite from Mt. Gut?i suggest that significant amounts of sialic crustal material were involved in their formation. The basalt from Raco? is from the vicinity of a deep fracture zone; its relatively low Sr⁸⁷/Sr⁸⁶ ratio suggests a direct link to a mantle source with little or no crustal contamination.     

Strontium isotope geochemistry of late cretaceous granodiorites,Jamaica and Haiti,greater Antilles

Initial⁸⁷Sr/⁸⁶Sr ratios have been determined for a representative suite of Upper Cretaceous granodiorites and associated rocks from the Above Rocks composite stock in central Jamaica and the Terre-Neuve pluton in northwestern Haiti. The average initial⁸⁷Sr/⁸⁶Sr ratio for severn samples of the Terre-Neuve intrusion is 0.7036, with a range of 0.7026–0.7047. For two samples of the Above Rocks the initial ratios are 0.7033 and 0.7034. A third sample from this intrusive has an initial ratio of 0.7084, which is tenatively attributed to contamination. The initial⁸⁷Sr/⁸⁶Sr ratios indicate that neither ancient sialic crust nor sediments carried down a Benioff zone can be the primary source of the granodioritic magma. K/Rb ratios for these rocks range from 178 to 247, which are much lower than the average values (≥1000) for tholeiitic basalts. It is concluded that the magmas originated primarily by melting of downthrust oceanic crust or adjacent mantle material.     

Volcanism in the Sumisu Rift, I. Major element, volatile, and stable isotope geochemistry

A bimodal volcanic suite with KAr ages of 0.05–1.40 Ma was collected from the Sumisu Rift using alvin. These rocks are contemporaneous with island arc tholeiite lavas of the Izu-Ogasawara arc 20 km to the east, and provide a present day example of volcanism associated with arc rifting and back-arc basin initiation. Major element geochemistry of the basalts is most similar to that of basalts found in other, more mature back-arc basins, which indicates that back-arc basins need not begin their magmatic evolution with lavas bearing strong arc signatures.Volatile concentrations distinguish Sumisu Rift basalts from island arc basalts and MORB. H₂O contents, which are at least four times greater than in MORB, suppress plagioclase crystallization. This suppression results in a more mafic fractionating assemblage, which prevents Al₂O₃ depletion and delays the initiation of Fe₂O_3^(tot) and TiO₂ enrichment. However, unlike arc basalts,Fe^3+/ΣFe ratios are only slightly higher than in MORB and are insufficient to cause magnetite saturation early enough to suppress Fe₂O_3^(tot) and TiO₂ enrichment. Thus, major element trends are more similar to those of MORB than arcs.H₂O, CO₂ and S are undersaturated relative to pure phase solubility curves, indicating exsolution of an H₂O-rich mixed gas phase. HighH₂O/S, highδD, and low (MORB-like)δ³⁴S ratios are considered primary and distinctive of the back-arc basin setting.     

Mineralogy and hydrogen isotope geochemistry of clay minerals in the Ohnuma geothermal area,Northeastern Japan

Mineralogical and hydrogen isotopic studies have been made on clay minerals occurring in the Ohnuma geothermal area, northeastern Japan. Here, clay minerals such as smectite, kaolinite, dickite, sericite, and chlorite were formed by hydrothermal alteration of Miocene rocks. A chemical equilibrium can be assumed to be attained from the fact that the amount of expandable layer in the interstratified chlorite/smectite decreases and the polytype of sericite changes from 1M to 2M₁ with increasing depth and temperature. The hydrogen isotopic composition (D/H) of the clay minerals is lighter than that of the geothermal and local meteoric waters by about 20–40‰. The hydrogen isotopic fractionation factors α_{mineral-water} are as follows: 0.972–0.985 for kaolinite and dickite, 0.973–0.977 for sericite, and 0.954–0.987 for chlorite. In the temperature range from 100 to 250°C, the hydrogen isotopic fractionation factors between these minerals and water are not sensitive to the temperature. α_{chlorite-water} depends on the kind of octahedrally coordinated cations which lie close to the hydroxyl groups; it becomes large with an increase of Mg content of chlorite.     

Rift Valley in the Atlantic Ocean near 36°50′N: petrology and geochemistry of basaltic rocks

Dredged rocks from an area of about 15 km² within the inner floor and on the adjacent walls of the Rift Valley were collected. Based on petrographic and chemical data, four types of basaltic rocks were recognized: (1) picritic basalts with olivine xenocrysts, TiO₂ < 0.6%, K₂O < 0.1%, (2) olivine basalts with olivine megacrysts, TiO₂ = 0.8–1.5%,K₂O = 0.1–0.2%, (3) highly phyric and moderately phyric plagioclase basalts with megacrystic plagioclase, TiO₂ < 1.3%, K₂O < 0.3%, and (4) pyroxene basalts with pyroxene > plagioclase, TiO₂ = 0.8–1%,K₂O = 0.2–0.4%. The Cr and Ni having high partition coefficients show different variation trends for each type of rock and their values decrease continuously as crystallization proceeds within each type of basalt. It is speculated that two different magmas have given rise to the above-mentioned rocks. One has yielded the picritic basalts and subsequently the olivine basalts after a separation of the olivine cumulates; the other gave rise to the plagioclase basalts.     

淮南采煤沉陷区积水水文地球化学及氢氧稳定同位素特征

以安徽淮南采煤沉陷积水为研究对象,通过样品采集与测试,研究不同沉陷年限及类型积水水文地球化学和氢氧稳定同位素组成特征及影响因素.结果表明：（1）研究区水化学类型主要为Cl-Na、HCO₃·Cl-Na型,沉陷积水中常量离子主要来源于蒸发岩溶解和硅酸盐风化,受蒸发作用和人为活动的影响明显,水化学组成随沉陷时间和类型变化不大.（2）淮南大气降水线方程为：δD=8.85δ¹⁸O+18.73,沉陷区积水氢氧稳定同位素值在淮南大气降水线右下方依次分布并接近降水线,表明沉陷积水主要来源于大气降水.（3）在降水稀释、水体蒸发及地下水补给的作用下,随着沉陷年限的增加,积水中重同位素越来越贫化,同一年限不同类型的积水同位素值变化较小.     

Volcanoes in the pre-Columbian life,legend, and archaeology of Costa Rica (Central America)

Costa Rica is located geographically in the southern part of the Central American Volcanic Front, a zone where interaction between the Mesoamerican and South American cultures occurred in pre-Columbian times. Several volcanoes violently erupted during the Holocene, when the first nomadic human hunters and later settlers were present. Volcanic rocks were the most important geo-resource in making artifacts and as construction materials for pre-Columbian inhabitants. Some pottery products are believed to resemble smoking volcanoes, and the settlements around volcanoes would seem to indicate their influence on daily life. Undoubtedly, volcanic eruptions disrupted the life of early settlers, particularly in the vicinity of Arenal and Irazú volcanoes, where archaeological remains show transient effects and displacement caused by periodical eruptions, but later resilient occupations around the volcanoes. Most native languages are extinct, with the exception of those presently spoken in areas far away from active volcanoes, where no words are related to volcanic phenomena or structures. The preserved legends are ambiguous, suggesting that they were either produced during the early Spanish conquest or were altered following the pre-Columbian period.     

SR isotope geochemistry of voluminous rhyolite of the Tamagawa Welded Tuffs, related rocks and andesite of the young volcanics, in Hachimantai geothermal area, Northeast Japan

The volcanic rocks from the Hachimantai geothermal area, Northeast Japan, are divided into the following five groups: (1) rhyolite of the Tamagawa Welded Tuffs (about 500 km³, 2.0–1.4 Ma); (2) andesite related to the Tamagawa Welded Tuffs (about 10 km³, 1.5 Ma); (3) andesite of the Matsukawa Andesite (about 100 km³, 1.8-1.2 Ma); (4) dacite of the Kashinai Formation (about 100 km³, 1.1 Ma); and (5) andesite of the Young Volcanics (about 300 km³, younger than 1 Ma). ratios of less-altered samples of the five groups range from 0.7038 to 0.7046. There is no significant difference in ratios among the five groups in spite of differences in age and chemical composition. Therefore, fusion of or contamination by old acidic crust can be ruled out for the genesis of the voluminous acidic magma which produced the rhyolite of the Tamagawa Welded Tuffs and the dacite of the Kashinai Formation.The low ratios and the chemistry suggest two possibilities for the genesis of the acidic rocks. One is a low degree of partial melting of the basic crust, which has a low ratio, under high temperature. Another is a high degree of fractional crystallization from basic magma derived from the mantle.     

The water content and hydrogen isotope composition of continental lithospheric mantle and mantle-derived mafic igneous rocks in eastern China

The water contents of minerals and whole-rock in mantle-derived xenoliths from eastern China exhibit large variations and are generally lower than those from other on- and off-craton lithotectonic units. Nevertheless, the water contents of mineral and whole-rock in Junan peridotite xenoliths, which sourced from the juvenile lithospheric mantle, are generally higher than those elsewhere in eastern China. This suggests that the initial water content of juvenile lithospheric mantle is not low. There is no obvious correlation between the water contents and Mg^# values of minerals in the mantle xenoliths and no occurrence of diffusion profile in pyroxene, suggesting no relationship between the low water content of mantle xenolith and the diffusion loss of water during xenolith ascent with host basaltic magmas. If the subcontinental lithospheric mantle (SCLM) base is heated by the asthenospheric mantle, the diffusion loss of water is expected to occur. On the other hand, extraction of basaltic melts from the SCLM is a more efficient mechanism to reduce the water content of xenoliths. The primary melts of Mesozoic and Cenozoic basalts in eastern China have water contents, as calculated from the water contents of phenocrysts, higher than those of normal mid-ocean ridge basalts (MORB). The Mesozoic basalts exhibit similar water contents to those of island arc basalts, whereas the Cenozoic basalts exhibit comparable water contents to oceanic island basalts and backarc basin basalts with some of them resembling island arc basalts. These observations suggest the water enrichment in the mantle source of continental basalts due to metasomatism by aqueous fluids and hydrous melts derived from dehydration and melting of deeply subducted crust. Mantle-derived megacrysts, minerals in xenoliths and phenocrysts in basalts from eastern China also exhibit largely variable hydrogen isotope compositions, indicating a large isotopic heterogeneity for the Cenozoic SCLM in eastern China. The water content that is higher than that of depleted MORB mantle and the hydrogen isotope composition that is deviated from that of depleted MORB mantle suggest that the Cenozoic continental lithospheric mantle suffered the metasomatism by hydrous melts derived from partial melting of the subducted Pacific slab below eastern China continent. The metasomatism would lead to the increase of water content in the SCLM base and then to the decrease of its viscosity. As a consequence, the SCLM base would be weakened and thus susceptible to tectonic erosion and delamination. As such, the crust-mantle interaction in oceanic subduction channel is the major cause for thinning of the craton lithosphere in North China.     

Stable hydrogen and oxygen isotope studies of rainfall and streamwaters for two contrasting holm oak areas of Catalonia, northeastern Spain

Results are presented of a study of stable hydrogen and oxygen isotopes in rainfall and streamwaters for the Montseny and Prades areas in northeastern Spain: results cover the full year of 1991. The isotopic pattern for rainfall is similar for both areas: there is a wide range in isotopic contents and the results show a strong, near-linear trend, δ²H = 7.9 × δ¹⁸O + 9.8 (N = 59; r² = 0.952), the ‘local meteoric line’. There is slight curvature to the data which may be related to the sources of water vapour forming the rainfall. Within the streams, the isotopic variability is much less than that of the rainfall although the data lie on, or very near to, the meteoric line. Data for detailed collections during storm events show more scatter than those collected regularly on a fortnightly basis. The event data show a linear feature that conforms to the local meteoric line. These results indicate that: (1) the main supply of water to the stream stormflow comes from water stored in the catchment prior to the event; (2) waters of more than one isotopic composition reside within the catchment and are transferable to the stream during storm events; (3) the main process of water transfer from the catchment back to the atmosphere comes from transpiration by the trees and (possibly) complete evaporation from the near-surface soil horizons and the tree canopy; (4) the isotopic technique cannot be used for quantitative hydrograph separation in this instance — at least two water types can be present within the catchment at any given time.     

Factors controlling stable oxygen,hydrogen and carbon isotope ratios in regional groundwater of the eastern United Arab Emirates (UAE)

Increasing groundwater salinity and depletion of the aquifers are major concerns in the UAE. Isotopes of oxygen, hydrogen, and carbon concentrations in groundwater were used to estimate evaporation loss using the isotopes of oxygen and hydrogen, and using a carbon isotope to trace inorganic carbon cycling in two main aquifers in the eastern part of the United Arab Emirates. The δD‐δ¹⁸O of groundwater samples plotted on a line given by: δD = 4 δ¹⁸O + 4 ·4 (r² = 0·4). In comparison, the local meteoric water line (LMWL) has been defined by the line: δD = 8 δ¹⁸O + 15. In order to better understand the system investigated, samples were separated into two groups based on the δD‐δ¹⁸O relationship. These are (1) samples that plot above the LMWL (δD = 6·1 δ¹⁸O + 12·4, r² = 0·8) and which are located predominantly in the north of the study area, and (2) samples that plot below the LMWL (δD = 5·6 δ¹⁸O + 6·2, r² = 0·8) and which are mostly distributed in the south. Slopes for both the groups are similar and lower than that for LMWL indicating potential evaporation of recharging water. However, the y‐intercept, which differs between the two groups, suggests evaporation of return flow and evapotranspiration in the unsaturated zone to be more significant in the south. This is attributed to intense agricultural activities in the region. Samples from the eastern Gravel Plain aquifer have δ¹³C and dissolved inorganic carbon (DIC) values in the range from ? 10 to 17‰, and 12–100 mg C/l, respectively, while the range for those from the Ophiolite aquifer is from ? 11 to ? 16.4‰, and 16–114 mg C/l respectively. This suggests the control of C‐3 and C‐4 plants on DIC formation, an observation supported by the range δ¹³C of soil organic matter (from ? 18·5 to ? 22·1‰.) Copyright © 2007 John Wiley & Sons, Ltd.     

Origin of waters responsible for serpentinization of the Izu-Ogasawara-Mariana forearc seamounts in view of hydrogen and oxygen isotope ratios

Many serpentinite seamounts occur over a region 20–120 km west of the trench axis in the Izu-Ogasawara-Mariana forearc regions. The hydrogen and oxygen isotopic compositions of serpentine from these regions indicate that there are at least two kinds of waters responsible for serpentinization: seawater and water derived from dehydration of the descending slab. Serpentine from two Mariana and two Torishima samples with microscopically ductile and sheared texture (sheared-type) have lowerδD(−63to−52‰) and slightly higherδ18O values (+6.1 to +8.2‰) than that of other nine Ogasawara samples with mesh texture (mesh-type) (δD= −43to−49‰ andδ¹⁸O= +5.8to+6.7‰). This suggests that the sheared-type serpentine with lowerδD and slightly higherδ¹⁸O values was formed within the wedge mantle by interaction with water derived from a descending slab. The sheared texture is likely to have been produced during diapiric uplift. The unaltered portion of the ultramafic bodies later interacted with seawater after emplacement at or near the seafloor, resulting in formation of the mesh-type serpentine with higherδD values.     

Oxygen and hydrogen isotope studies of serpentinization in the Troodos ophiolite complex,Cyprus

Oxygen and hydrogen isotopic compositions were measured on 12 serpentine and 2 actinolite samples from the Troodos ophiolite complex, Cyprus. The single analyzed antigorite(δD= ?60, δ¹⁸O= 7.1) is isotopically similar to all previously analyzed antigorites from ultramafic bodies. However, although their D/H ratios are relatively “normal”(δD= ?70to?92), the δ¹⁸O values of most of the Troodos lizardite-chrysotile serpentines (+12.6 to +14.1) are much higher than the 2.0–9.3‰ range typically found in such serpentines. Such high δ¹⁸O values have previously been found only in the serpentine-like mineraloids termed “deweylites”, which apparently formed at Earth-surface temperatures, and in a single sample from Vourinos, Greece that is in contact with high-¹⁸O limestone. The Troodos lizardite-chrysotile samplescannot have formed by reaction with heated ocean waters, but instead must have formed in contact with large amounts of some type of meteoric, metamorphic, or formation water, either (1) at very low temperatures in a near-surface environment, or (2) at about 100°C from waters that were abnormally enriched in¹⁸O(δ¹⁸O ≈ +4 to +8). The latter possibility seems most plausible inasmuch as extensive evaporites were deposited throughout the Mediterranean Sea during the late Miocene, and this would have been accompanied by strong¹⁸O enrichments of the local meteoric waters. Heated ocean waters, however, probably were responsible for the formation of the actinolitic amphiboles(δ¹⁸O= 4.6 to 5.5; δD= ?51to?46) from the gabbro and ultramafic zones in the Troodos complex. The amphiboles must have formed at considerably higher temperatures and at an earlier stage than the lizardite-chrysotile serpentinization.     

Sr, Nd isotope geochemistry of volcanic rock series and its geological significance in the middle Okinawa Trough

There exists extensive basic-acidic volcanic rock series in the middle section of the Okinawa Trough. Different types of these volcanic rocks have their own average strontium ratios of 0.704 749, 0.705 062, 0.708 771, 0.704 840 and 0.720 301 with average¹⁴³Nd/¹⁴⁴Nd ratios of 0.512 820, 0.512 673, 0.512 413, 0.512 729 and 0.512 034. These ratios of Sr and Nd isotopes all fall on a theoretic hyperbolic curve of mixing between two end-members of MORB and rhyolitic magma. So we infer that these different kinds of volcanic rocks in the middle Okinawa Trough are the erupted product in different stages of formation and evolution of the trough crust. MORB magma, which had suffered assimilation, mixed with the early-formed crust-derived rhyolitic partial melt mass at different ratios; then, these mixed magma erupted and formed volcanic rock types of the trough. This study indicates that the Okinawa Trough is coming into a stage of submarine spreading from the stage of continental rift.     

(40)~Ar/(39)~Ar chronology and geochemistry of high-K volcanic rocks in the Mangkang basin, Tibet

Our two newly obtained high-quality 40Ar/39Ar ages suggest that the high-K volcanic rocks of the Lawuxiang Formation in the Mangkang basin, Tibet were formed at 33.5±0.2 Ma. The tracing of elemental and Pb-Sr-Nd isotopic geochemistry indicates that they were derived from an EM2 enriched mantle in continental subduction caused by transpression. Their evidently negative anomalies in HFSEs such as Nb and Ta make clear that there is an input of continental material into the mantle source. The high-K rocks at 33.5±0.2 Ma in the Mangkang basin may temporally, spatially and compositionally compare with the early one of two-pulse high-K rocks in eastern Tibet distinguished by Wang J. H. et al., implying that they were formed in the same tectonic setting.     

The 322 ka Tiribí Tuff: stratigraphy, geochronology and mechanisms of deposition of the largest and most recent ignimbrite in the Valle Central, Costa Rica

The Tiribí Tuff covered much of the Valle Central of Costa Rica, currently the most densely populated area in the country (∼2.4 million inhabitants). Underlying the tuff, there is a related well-sorted pumice deposit, the Tibás Pumice Layer. Based on macroscopic characteristics of the rocks, we distinguish two main facies in the Tiribí Tuff in correlation to the differences in welding, devitrification, grain size, and abundance of pumice and lithic fragments. The Valle Central facies consists of an ignimbritic plateau of non-welded to welded deposits within the Valle Central basin and the Orotina facies is a gray to light-bluish gray, densely to partially welded rock, with yellowish and black pumice fragments cropping out mainly at the Grande de Tárcoles River Gorge and Orotina plain. This high-aspect ratio ignimbrite (1:920 or 1.1×10⁻³) covered an area of at least 820 km² with a long runout of 80 km and a minimum volume outflow of 25 km³ (15 km³ DRE). Geochemically, the tuff shows a wide range of compositions from basaltic-andesites to rhyolites, but trachyandesites are predominant. Replicate new ⁴⁰Ar/³⁹Ar age determinations indicate that widespread exposures of this tuff represent a single ignimbrite that was erupted 322±2 ka. The inferred source is the Barva Caldera, as interpreted from isopach and isopleth maps, contours of the ignimbrite top and geochemical correlation (∼10 km in diameter). The Tiribí Tuff caldera-forming eruption is interpreted as having evolved from a plinian eruption, during which the widespread basal pumice fall was deposited, followed by fountaining pyroclastic flows. In the SW part of the Valle Central, the ignimbrite flowed into a narrow canyon, which might have acted as a pseudo-barrier, reflecting the flow back towards the source and thus thickening the deposits that were filling the Valle Central depression. The variable welding patterns are interpreted to be a result of the lithostatic load and the influence of the content and size of lithic fragments.     

Sr–Nd isotope ratios of gabbroic and dioritic rocks in a Cretaceous-Paleogene granite terrain, Southwest Japan

Abstract Whole‐rock chemical and Sr and Nd isotope data are presented for gabbroic and dioritic rocks from a Cretaceous‐Paleogene granitic terrain in Southwest Japan. Age data indicate that they were emplaced in the late Cretaceous during the early stages of a voluminous intermediate‐felsic magmatic episode in Southwest Japan. Although these gabbroic and dioritic rocks have similar major and trace element chemistry, they show regional variations in terms of initial Sr and Nd isotope ratios. Samples from the South Zone have high initial ⁸⁷Sr/⁸⁶Sr (0.7063–0.7076) and low initial Nd isotope ratios (?_Nd, ?2.5 to ?5.3); whereas those from the North Zone have lower initial ⁸⁷Sr/⁸⁶Sr (usually less than 0.7060) and higher Nd isotope ratios (?_Nd, ?0.8 to + 3.3). Regional variations in Sr and Nd isotope ratios are similar to those observed in granitic rocks, although gabbroic and dioritic rocks tend to have slightly lower Sr and higher Nd isotope ratios than granitic rocks in the respective zones. Limited variations in Sr and Nd isotope ratios among samples from individual zones may be attributed partly to a combination of upper crustal contamination and heterogeneity of the magma source. Contamination of magmas by upper crustal material cannot, however, explain the observed Sr and Nd isotope variations between samples from the North and South Zones. Between‐zone variations would reflect geochemical difference in magma sources. The gabbroic and dioritic rocks are enriched in large ion lithophile elements (LILE) and depleted in high field strength elements (HFSE), showing similar normal‐type mid‐ocean ridge basalt (N‐MORB) normalized patterns to arc magmas. Geochronological and isotopic data may suggest that some gabbroic and dioritic rocks are genetically related to high magnesian andesite. Alternatively, mantle‐derived mafic or intermediate rocks which were underplated beneath the crust may be also plausible sources for gabbroic and dioritic rocks. The magma sources (the mantle wedge and lower crust) were isotopically more enriched beneath the South Zone than the North Zone during the Cretaceous‐Paleogene. Sr and Nd isotope ratios of the lower crustal source of the granitic rocks was isotopically affected by mantle‐derived magmas, resulting in similar initial Sr and Nd isotope ratios for gabbroic, dioritic and granitic rocks in each zone.