Oxygen isotopic compositions of Central Andean plutonic and volcanic rocks,latitudes 26°–29° south

Oxygen isotope data are reported for 27 igneous rocks of Mesozoic to Quaternary age from the Central Andes. 26–29°S. The plutonic rocks, and most of the volcanics, have δ¹⁸O values between 6.2 and 8.3‰.The whole-rock δ¹⁸O values show a weak correlation with initial⁸⁷Sr/⁸⁶Sr data. This O-Sr array differs from documented trends for calc-alkaline plutonic suites from California, Scotland and northern Italy, but overlaps with data for volcanic and plutonic rocks from Ecuador, northern Chile and southern Perú.The oxygen isotope results indicate that the magmas evolved without significant contamination from supracrustal rocks (e.g., rocks that experienced¹⁸O enrichment during surficial weathering). The available O, Sr and Pb isotopic data for these rocks are best explained by magma generation in the upper mantle or lower crust. From the Late Mesozoic on, the⁸⁷Sr/⁸⁶Sr values were modified at depth by isotopic exchange between the magma and a continually thickening crust of plutonic rocks of Late Precambrian to early Mesozoic age.     

Oxygen and strontium isotopic characteristics of calc-alkalic volcanic rocks from the central and western Japan arcs: Evaluation of contribution of crustal components to the magmas

¹⁸O/¹⁶O and ⁸⁷Sr/⁸⁶Sr ratios were determined for Quaternary calc-alkalic volcanic rocks from six volcanic rock suites in the central and western Japan arcs. The δ¹⁸O values relative to SMOW and ⁸⁷Sr/⁸⁶Sr ratios range from +6.3 to +9.9⁰/₀₀ and 0.70357 to 0.70684, respectively. Both the O- and Sr-isotopic compositions are higher than those for island-arc primitive magmas and their differentiates. The isotopic compositions of the calc-alkalic rocks cannot be derived by a simple fractional crystallization of the primitive magmas. On the other hand, the ¹⁸O- and ⁸⁷Sr-enrichment is confined to the rock suites located in well-developed island arcs having thick continental-type crust with low or negative Bouguer anomalies. Involvement of ¹⁸O- and ⁸⁷Sr-rich crustal material in the magma formation is suggested.The isotopic compositions vary remarkably within individual rock suites as well as from volcano to volcano. The data points in δ¹⁸O vs. ⁸⁷Sr/⁸⁶Sr plot accord with a mixing model between primitive magmas and crustal material of dioritic composition on an average, assuming their comparative Sr contents. The primitive magmas involved could not be low-Sr tholeiites, but magmas more or less enriched in incompatible elements including Sr, which correspond to high-alkali tholeiites or alkali basalts and their evolved magmas. The nature of the primitive magmas seems to change from tholeiitic to more alkalic with progressing island-arc evolution.Mixing of crust-derived melts is more plausible than assimilation of solid-rocks for involving 20 to 30% crustal material in the magmas along simple mixing curves. Isotopic variations between the rock suites are ascribed to variable Sr concentration radio of the end-members, variable isotopic compositions of crustal material or variable mixing ratio of the end-members. Extremely high-δ ¹⁸O rocks with moderate increase in ⁸⁷Sr/⁸⁶Sr ratio suggest another mixing process in shallower magma chambers between andesite magmas and metasedimentary rocks having high δ ¹⁸O and ⁸⁷Sr/⁸⁶Sr values but low Sr content. Subsequent fractional crystallization of once-derived magmas would be the prominent process for the rock suites showing gradual increase in ¹⁸O up to 1⁰/₀₀ with uniform ⁸⁷Sr/⁸⁶Sr ratios.     

Chemistry of volcanic rocks and seismicity of the earth’s Mantle in the Island arcs

Volcanic belts in island ares are associated in space with epicenter belts of mantle earthquakes. Primary magma of volcanoes on the oceanic side of an island are is rich in silica and poor in alkalies. In contrast, it is poor in silica and rich in alkalies on the continental side. Foci of the mantle carthquakes are close to a plane that dips away from the oceanic side toward the continental side. The spatial correlation between nature of primary magmas and depth of earthquake foci suggests a common origin. Moreover, the hypothesis that the generation of magma and the occurrence of mantle earthquakes are genetically related and that the primary magmas in the island ares are generated at levels about 150 to 250 km deep. is supported by the relationship among dillerent island ares, that is, primary magma of volcanoes fronting on oceanic trenches becomes more silicious from one are to another as the seismicity of mantle earthquake zones becomes greatre.     

Petrogenesis of Cenezoic volcanic rocks from the Aegean island arc

The Aegean volcanic arc formed in response to northeasterly subduction of the Mediterranean sea floor beneath the Aegean Sea. The active arc lies over 250 km from the Hellenic Trench in a region which has suffered considerable extension and subsidence since the mid-Tertiary. Suites of samples from the different volcanic centres making up the arc have been studied geochemically in order to assess lateral variations and to constrain the contribution of crustal contamination and sediment subduction in their petrogenesis.Lavas from all the major volcanic centres exhibit typical calc-alkaline major-element characteristics, and show enrichment in light REE and LIL elements but low contents of HFS elements. The enrichment in light REE is greater in the eastern (Nisyros, Kos) and western (Milos, Poros, Methana, Aegina) sectors of the arc (Ce_n/Yb_n=4) than in the central Santorini sector (Ce_n/Yb_n=2). All lavas have significant negative Eu anomalies and many have slight negative Ce anomalies. Less coherence is observed in the abundances and ratios of the other LIL elements, compared with the REE, along the island chain.Whereas the effects of crystal fractionation are evident in the trace-element patterns of lavas from individual islands, and are particularly well marked for Santorini, it is clear that there are consistent differences in trace-element abundances and ratios in the lavas of the various islands which reflect compositional differences in the mantle source and/or in melting conditions. Lavas from the eastern and western sectors have much higher levels of Ba and Sr but relatively lower Th, K and Rb than those from Santorini. Although some geochemical features could be explained through involvement of a component of subducted sediment in the source regions of the volcanoes, other element abundances and ratios indicate that this component must be very small. Detailed consideration of the inter-island geochemical variations suggests a complex make-up of the underlying lithosphere, resulting from a long history of subduction. In the region of Santorini, where crustal stretching is greatest, the underlying asthenosphere may be involved in magma production.     

Nd and Sr isotopic study of volcanic rocks from Japan

Two older granitic rocks and some selected Quaternary volcanic rocks from the Japanese Islands were analyzed in a reconnaissance study for the purpose of examining the relationships between Nd and Sr isotopic abundances and the megatectonic structure around the Japanese Islands. Model ages of ～0.9 AE were determined by the Nd and Sr methods on a Paleozoic gneiss which confirms that a relatively ancient acidic basement exists in the Japanese Islands. The Nd and Sr isotopic data show that the Cretaceous granodiorite is the result of partial melting of older crust.The Nd of tholeiitic rocks from the Izu arc gives ε_Nd ranging from 8.3 to 9.3 and with the corresponding ε_Sr from ?14.5 to ?18.5. These results are identical to those found for the Mariana arc. These values are distinctly lower than typical MORB by around 1～2 εu. This difference in ε_Nd between arcs and MORB is attributed to the contribution of oceanic sediments to the partial melts produced during subduction of oceanic crust. The Hakone volcano is clearly confirmed as belonging to an oceanic source by Nd isotopic results.ε_Sr-ε_Nd values of the volcanics from a section along the Fossa Magna show a clear indication that they are a blend of oceanic mantle material and continental crustal material. The crustal component clearly increases in going from south to north. Volcanics across the Northeast Japan arc also show a distinct correlation of ε_Sr-ε_Nd related to the position relative to the active subduction zone but with the opposite trend. These relationships of the present isotopic pattern and the zonal arrangement relative to the subduction zone suggest the former existence of a local spreading center in the Japan Sea.In general there appear to be regular isotopic relationships between the Izu-Mariana oceanic island arc and the continental island arc of Japan which indicates that partially melted or assimilated older continental basement is admixed with young rising oceanic arc magmas.     

The origin of ocean island basalt end-member compositions: trace element and isotopic constraints

Ocean island basalt (OIB) suites display a wide diversity of major element, trace element, and isotopic compositions. The incompatible trace element and isotopic ratios of OIB reflect considerable heterogeneity in the mantle source regions. In addition to the distinctive Sr, Nd and Pb isotopic signatures of the HIMU, EMI and EMII OIB end-members, differences in incompatible trace element ratios among these end-members are of great help in identifying the nature and origin of their sources. Examination of trace element and isotopic constraints for the three OIB end-members suggests a relatively simple model for their origin. The dominant component in all OIB is ancient recycled basaltic oceanic crust which has been processed through a subduction zone, and which carries the trace element and isotopic signature of a dehydration residue (enrichment in HFSE relative to LILE and LREE, low Rb/Sr, but high U/Pb and Th/Pb ratios leading to the development of radiogenic Pb isotope compositions). HIMU OIB are derived from such a source, with little contamination from other components. Both the EMI and EMII OIB end-members are also dominantly derived from this source, but they contain significant proportions (up to 5–10%) of sedimentary components derived from the continental crust. In the case of EMI OIB, ancient pelagic sediment with high LILE/HFSE, LREE/HFSE, Ba/Th and Ba/La ratios, and low U/Pb ratios, is the contaminant. EMII OIB are also contaminated by a sedimentary component, in the form of ancient terrigenous sediment with high LILE/HFSE and LREE/HFSE ratios, but lacking relative Ba enrichment, and with higher U/Pb and Rb/Sr ratios. A model whereby the source for all OIB is ancient (1–2 Ga old) subducted oceanic crust ± entrained sediment (pelagic and/or terrigenous) is therefore consistent with the trace element and isotopic data. Although subducted oceanic lithosphere will accumulate and be dominantly concentrated within the mesosphere boundary layer, forming the source for hot-spots, such material may also become convectively dispersed within the depleted upper mantle as blobs or streaks, giving rise to small-scale chemical heterogeneities in the upper mantle.     

On the lateral variations in chemical composition and volume of quaternary volcanic rocks across Japanese arcs

The Fe/Mg+Fe) ratios (X_Fe) of the Quaternary basalts (SiO₂ < 53 wt.%) in the Japanese arcs were examined. The X_XFe of relatively magnesian basalts decreases from the volcanic front toward the Japan Sea across the arcs. Based on the partition coefficient of Mg-Fe²⁺ between olivine and liquid, it is suggested that all the basalts near the volcanic front, which are mostly tholeiitic basalts, are significantly fractionated, whereas many basalts near the Japan Sea, which are mostly alkali basalts, are little fractionated. The K₂ O content in the primary basalt magmas increases toward the Japan Sea. Combining the X_Fe and K₂ O data, it is suggested that relatively large amounts of tholeiitic magmas are produced near the volcanic front, but they fractionate during their ascent, whereas smaller amounts of alkali basalt magmas are formed near the Japan Sea, but they can ascend with less fractionation. The density of primary tholeiite magma is significantly larger than that of primary alkali basalt magmas. It is most likely that primary tholeiite magmas cannot ascend beyond the upper crust and would fractionate to produce less dense tholeiitic magmas near the volcanic front, whereas primary alkali basalt magmas can ascend through the upper crust without fractionation, as far as buoyancy is the principal ascending force. In the Japanese arcs, the stress field may be less compressional near the Japan Sea than near the volcanic front, so that magmas can ascend more rapidly in the latter region than in the former. These two factors may be responsible for the above mentioned chemical variations of basalt magmas across the arcs. The variation in volume of the Quaternary volcanic rocks across the arcs can be explained by the presence of a melt-rich zone above but nearly parallel to the subducted slab.     

Inert gas abundances in basalts of the Lesser Antilles island arcs: possible implications for their volcanic evolution

Measurements of noble gas element abundances in igneous rock samples from the Lesser Antilles island arc (LAIA) show an enrichment of Ne, Kr and Xe relative to Ar, when compared to the atmospheric inert gas composition. The element concentrations vary as a function of time and a cyclic variation appears to occur in the pre-Pliocene stage of arc development. The pattern of elemental abundances closely resembles that of ocean floor basalts, suggesting that, (1) the origin of the inert gases in these samples is related to the subduction of oceanic lithosphere responsible for the formation of the LAIA, and (2) the subduction process does not modify the noble gas patterns of the materials being subducted.There is no evidence of a change in concentration or composition of noble gases occurring at ca. 9 Ma, the time when it has been suggested the LAIA shifted to form the western, younger, volcanic Caribbees. However, a major hiatus in the noble gas evolution is recognised at ca. 16 Ma.     

Petrology of the volcanic rocks of saba,West Indies

Saba is composed of basic and intermediate members of the calc alkaline series with a broad resemblance to volcanic rocks on other islands of the northern Lesser Antilles. The most abundant rock-type is hornblende andesite with relatively high potassium and associated elements. Notable petrographic features are the persistence of magnesian olivine into relatively siliceous whole-rock composition and the prevalence of hornblende even in the more basic rocks. Quartz xenocrysts also occur in the basalts Clinopyroxene phenocrysts are of an gite composition but groundmass grains are sometimes in the range subcalcic augite to magnesian pigeonite. Disequilibrium features in the petrography, together with anomalies in the chemical trends may be due to incorporation of xenocrysts or perhaps in extreme instances to the hybridisation of contrasting magmas.     

Helium isotopic variations in volcanic rocks from Loihi Seamount and the Island of Hawaii

Helium isotopic ratios ranging from 20 to 32 times the atmospheric ³He/⁴He(R_A) have been observed in a suite of 15 basaltic glasses from the Loihi Seamount. These ratios, which are up to four times higher than those of MORB glasses and more than twice those of nearby Kilauea, are strongly suggestive of a primitive source of volatiles supplying this volcanism. The Loihi glasses measured span a broad compositional range, and the ³He/⁴He ratios were found to be generally lower for the alkali basalts than for the tholeiites. The component with a lower ³He/⁴He ratio appears to be associated with olivine xenocrysts, within which fluid inclusions are probably the carrier of contaminant helium. One Loihi sample has a much lower isotopic ratio (<5 R_A), but a combination of low He concentration, high vesicularity, and presence of cracks lined with clay minerals suggests that the low ratio is due to gas loss and contamination by atmospheric helium.Crushing and melting experiments show that for modest vesicularities (<5% by volume) the Loihi glasses obey a MORB-type partitioning trend, but at higher vesicularities the data show considerably more scatter due to volatile mobilization. The high vesicularities, low extrusion pressure and generally low helium concentrations are consistent with a considerable degree of degassing. Analyses of dunites, plus a correlation between total helium concentrations with xenocryst abundances also suggest that xenocrysts are a significant carrier of contaminating (low ³He/⁴He) helium.³He/⁴He ratios from samples of other Hawaiian volcanoes (Kilauea, Mauna Loa, Hualalai, and Mauna Kea) show a smooth decrease in ³He/⁴He with increasing volcano age and volume. We interpret this to be a synoptic picture of the time evolution of a hot-spot diapir: the earliest stage is characterized by primitive (> 30 R_A) helium with some (variable) component of lithospheric contamination added during “breakthrough”, while the later stages are characterized by a relaxation toward lithospheric ³He/⁴He ratios (～ 8 R_A) due to isolation of the diapir from the mantle below (as the plate moves on), and subsequent mining of the inherited helium and contamination from the surrounding lithosphere. The abrupt contrast in ³He/⁴He ratios between Kilauea and Loihi, despite their close proximity, is indicative of the small lateral extent of the plume.     

Petrology of the volcanic rocks of martinique,West Indies

Volcanological differences between the old and the recent lavas from Martinique, Lesser Antilles, are presented, showing that two volcanic series exist in this island:

Dash

a high-alumina basalt series generally mafic, line-grained, partly pillowed, with clinopyroxene-rich lavas which show iron enrichment tendancies en an A.F.M. plot;

a calc-alkaline (slightly potassic) series much more siliceous as a group, porphyric, predominantly sub-aerially erupted with orthopyroxene-rich lavas which show no iron enrichment.

The high-alumina basalt series is considered as having originated from a differentiation trend by fractionation of olivine, clinopyroxene and plagioclase. Lavas range from olivine basalt to tridymite-rich dacite. The calc-alkaline series probably derives from the contamination of the first suite but the occurence of hornblende-rich cumulates indicates the process of fractionation takes place too. Lavas range from orthopyroxene andesite and hornblende andesite to quartz-hornblende dacite and quartz-biotite dacite.     

Trace-element and isotopic constraints on the source of magmas in the active volcano and Mariana island arcs, Western Pacific

Analytical results of the relative and absolute abundance of LIL-incompatible trace elements (K, Rb, Cs, Sr, and Ba) and isotopic compositions ( , , and ) are summarized for fresh samples from active and dormant volcanoes of the Volcano and Mariana island arcs. The presence of thickened oceanic crust (T 15–20 km) beneath the arc indicates that while hybridization processes resulting in the modification of primitive magmas by anatectic mixing at shallow crustal levels cannot be neglected, the extent and effects of these processes on this arc's magmas are minimized. All components of the subducted plate disappear at the trench. This observation is used to reconstruct the composition of the crust in the Wadati-Benioff zone by estimating proportions of various lithologies in the crust of the subducted plate coupled with analyses from DSDP sites. Over 90% of the mass of the subducted crust consists of basaltic Layers II and III. Sediments and seamounts, containing the bulk of the incompatible elements, make up the rest. Bulk Western Pacific seafloor has , δ ¹⁸O +7.2, K/Rb 510, K/Ba 46, and K/Cs 13,500. Consideration of trace-element data and combined systematics limits the participation of sediments in magmagenesis to less than 1%, in accord with the earlier results of Pb-isotopic studies. Combined data indicate little, if any, involvement of altered basaltic seafloor in magmagenesis. Perhaps more important than mean isotopic and LIL-element ratios is the restricted range for lavas from along over 1000 km of this arc. Mixtures of mantle with either the subducted crust or derivative fluids should result in strong heterogeneities in the sources of individual volcanoes along the arc. Such heterogeneities would be due to: (1) gross variations of crustal materials supplied to the subduction zone; and (2) lesser efficiency of mixing processes accompanying induced convection between arc segments (parallel to the arc) as compared to that perpendicular to the arc. The absence of these heterogeneities indicates that either some process exists for the efficient mixing of mantle and subducted material parallel to the arc or that subducted materials play a negligible role in the generation of Mariana-Volcano arc melts.Consideration of plausible sources in the mantle indicates that (1) an unmodified MORB-like mantle cannot have generated the observed trace-element and isotopic composition of this arc's magmas, while (2) a mantle similar to that which has produced alkali-olivine basalts (AOB) of north Pacific “hot spot” chains is indistinguishable in many respects spects from the source of these arc lavas.     

Molecular and carbon isotopic compositions of gas inclusions of deep carbonate rocks in the Tarim Basin

Gaseous components of gas inclusions in deep carbonate rocks (>5700 m) from the Tacan 1 well were analyzed by online mass spectrometry by means of either the stepwise heating technique or vacuum electromagnetism crushing. The carbon isotopic compositions of gases released by vacuum electromagnetism crushing were also measured. Although the molecular compositions of gas inclusions show differences between the two methods, the overall characteristics are that gas inclusions mainly contain CO2, whilst hydrocarbon gases, such as CH4, C2H6 and C3H8, are less abundant. The content of CO is higher in the stepwise heating experiment than that in the method of vacuum electromagnetism crushing, and there are only minor amounts of N2, H2 and O2 in gas inclusions. Methane δ13C values of gas inclusions in Lower Ordovician and Upper Cambrian rocks (from 5713.7 to 6422 m; -52‰-63‰) are similar to those of bacterial methane, but their chemical compositions do not exhibit the dry character in comparison with biogenic gases. These characteristics of deep gas inclusions may be related to the migration fractionation. Some deep natural gases with light carbon isotopic characteristics in the Tazhong Uplift may have a similar origin. The δ13C1 values of gas inclusions in Lower Cambrian rocks (7117-7124 m) are heavier (-39‰), consistent with highly mature natural gases. Carbon isotopic compositions of CO2 in the gas inclusions of deep carbonate rocks are similar (from -4‰ to -13‰) to those of deep natural gases, indicating predominantly an inorganic origin.     

Petrochemical affinities of volcanic rocks from the tonga — Kermadec island arc,Southwest Pacific

Eruptive suites from Tonga (tholeiitic), Raoul Island (tholeiitic) and Macauley Island (high-alumina) are characterised by low alkalis, an absence of andesites in the range 56–65% silica, and restricted acidity for minor glassy differentiates (SiO₂=65–68 %). These volcanics form a chain of islands overlying a seismic zone which extends from Tonga to the central volcanic region of North Island, New Zealand where a calc-alkaline series contains basaltic, andesitic and rhyolitic members in that order of increasing abundance. Within this continental suite, tholeiitic and high-alumina phases are recognised as closely similar to the intra-oceanic Tonga-Kermadec magma types and show petrochemical gradation into the medium-silica andesites, apparently by sialic assimilation.     

Batch fractionation model for the evolution of volcanic rocks in an island arc: an example from Central Japan

Analyses of fifty-one rock samples from three stratovolcanoes in Central Japan revealed that K and Rb contents vary in a saw-toothed fashion with the growth of these volcanoes. Peaks and valleys of the saw-toothed variation pattern of Rb (and also K) increase at first and then gradually converge on constant values. This variation trend is also shown by the Rb/Sr ratio. The convergent Rb/Sr ratio (0.23–0.24) at the peaks coincides with recent estimates of the average value for continental crust. These geochemical features are well explained by the batch fractionation model. In this model, the magma reservoir lying at the top of the mantle is periodically supplied with a batch of parental magma, while the magma in it undergoes continuous crystallization and the cumulate is continuously removed by the divergent movement of the mantle. This model, working under physical conditions in the crust-mantle structure of an island arc, not only accounts for the above geochemical features, but also gives insight into the genesis of the calc-alkaline rock series and of the continental crust.     

The composition and differentiation of the volcanic rocks of Carriacou,grenadines, West Indies

Tertiary volcanic rocks of Carriacou occupy two-thirds of the island. The volcanics include volcaniclastics, lava flows and dome lavas and range in composition from basalts to andesites. Carriacou basalts fall into two petrographic types (a) clinopyroxene-plagioclase-phyric basalts and (b) olivine microphyric basalts; the latter having higher MgO and lower Al₂O₃ than the clinopyroxene basalts. Both types are unusually rich in mafic minerals compared with Lesser Antilles basalts in general, although similar types have been reported from the nearby island of Grenada. The potash to silica ratios are relatively high and confirm the similarity between Carriacou and Grenada basalts and the differences between these basalts and basalts from other islands of the Lesser Antilles. The basaltic andesites and andesites from Carriacou correspond closely in mineralogical and chemical composition with typical andesites found elsewhere in the Lesser Antilles. The geochemistry of the volcanics shows that the olivine microphyric basalts display tholeiitic affinities whereas the clinopyroxeneplagioclase-phyric basalt, basaltic andesites and andesites are calcalkaline. The compositional gradation in both the geochemistry and mineralogy of these volcanics suggests that fractional crystallization played an important role in the derivation of the various magma.     

Possible origin of K-rich volcanic rocks from Virunga,East Africa,by metasomatism of continental crustal material: Pb,Nd and Sr isotopic evidence

The isotopic compositions of Sr, Nd and Pb together with the abundances of Rb, Sr, U and Pb have been determined for mafic and felsic potassic alkaline rocks from the young Virunga volcanic field in the western branch of the East African rift system.⁸⁷Sr/⁸⁶Sr varies from 0.7055 to 0.7082 in the mafic rocks and from 0.7073 to 0.7103 in the felsic rocks. The latter all come from one volcano, Sabinyo. Sabinyo rocks have negative ε_Ndvalues ofε_Nd = ?10. Nd and Sr isotopic variations in the basic potassic rocks are correlated and plot between Sabinyo and previously reported [1] compositions (ε_Nd = +2.5;⁸⁷Sr/⁸⁶Sr≈ 0.7047) for Nyiragongo nephelinites. The Pb isotopic compositions for Sabinyo rocks are nearly uniform and average²⁰⁶Pb/²⁰⁴Pb≈ 19.4,²⁰⁷Pb/²⁰⁴Pb= 15.79–15.84,²⁰⁸Pb/²⁰⁴Pb≈ 41.2. The basic potassic rocks have similar²⁰⁶Pb/²⁰⁴Pb values but range in²⁰⁷Pb/²⁰⁴Pb and²⁰⁸Pb/²⁰⁴Pb from the Sabinyo values to less radiogenic compositions.Excellent correlations of⁸⁷Sr/⁸⁶Sr with Rb/Sr, 1/Sr and²⁰⁷Pb/²⁰⁶Pb for Sabinyo rocks suggest these to be members of a hybrid magma series. However, the nearly uniform Pb compositions for this series points to radiogenic growth of⁸⁷Sr in the magma source region following an event which homogenized the isotopic compositions but not Rb/Sr. The Rb-Sr age derived from the erupted Sabinyo isochron-mixing line is consistent with the ～500 Myr Pb-Pb age from Nyiragongo [1], which suggests that this event affected all Virunga magma sources. The event can again be traced in the Pb-Pb, Pb-Sr and Nd-Sr isotopic correlations for all Virunga rocks, including Nyiragongo, when allowances are made for radiogenic growth subsequent to this mixing or incomplete homogenization event. Inferred parent/daughter element fractionations point to a metasomatic event during which a mantle fluid invaded two lithospheric reservoirs: a +ε_Nd reservoir sampled by the Nyiragongo nephelinites and suggested to be the subcontinental mantle and a ?ε_Nd reservoir sampled by the mafic and felsic potasssic volcanism. Whether this ?ε_Nd reservoir is the crust, continental crustal material in the mantle or anomalous mantle cannot be decided from the data. The simplest answer, that this reservoir is the continental crust, seems to be at variance with experimental evidence suggesting a subcrustal origin for basic potassic magmas. Partial melting of the ancient metasomatised lithospheric domains and ensuing volcanism seems to be entirely a response to decompression and rising geotherms during rifting and thinning of the lithosphere.     

Cenozoic volcanic rocks of eastern China — secular and geographic trends in chemistry and strontium isotopic composition

The Cenozoic volcanic rocks of eastern China are subalkalic to alkalic basalts erupted in an early Tertiary back-arc rift environment and from scattered late Tertiary and Quaternary volcanic centers in a continental area crossed by active faults, driven by subduction of the Pacific plate and the collision of India and Eurasia. Immobile trace elements and major elements conform very well to each other in classification of the 59 rocks for which complete data are reported and they correctly identify the tectonic setting. LIL-element enrichments of the basalts lie between those of P-MORB and ocean island alkalic basalts, and show a secular increase.⁸⁷Sr/⁸⁶Sr ratios of basalts vary from 0.7029 to 0.7048. Alkalic basalts are systematically less radiogenic than geographically coextensive and contemporaneous tholeiitic basalts. Increase of radiogenic Sr with increasing crustal thickness and crustal age and with silica enrichment of the magmas suggests crustal contamination but this is inadequate to explain the LIL-element enrichment patterns and variable LIL-element enrichments. The preferred hypothesis is that the alkalic magmas come from a deeper source, with long-term LIL-element depletion and low Rb/Sr ratio but relatively recent LIL-element enrichment. Conversely the tholeiitic magmas are melts of subcontinental mantle lithosphere that is more LIL-element depleted than the alkalic source, at the time of magma genesis, but has had an elevated Rb/Sr ratio for much of its post-consolidation history.     

Hydrogeochemical and isotopic evidence of groundwater salinization in a coastal aquifer: a case study in Jeju volcanic island, Korea

In order to identify the origin of saline groundwater in the eastern part of Jeju volcanic island, Korea, a hydrogeochemical and isotopic study has been carried out for 18 observation wells located in east and southeast coastal regions. The total dissolved solid contents of groundwaters are highly variable (77–21,782 mg/l). Oxygen, hydrogen, sulfur, and strontium isotopic data clearly show that the saline water results from mixing of groundwater with seawater. Strontium isotopic compositions and Br/Cl and I/Cl ratios strongly suggest that the source of salinity is modern seawater intrusion. Hydrogeochemical characteristics based on bivariate diagrams of major and minor ions show that changes in the chemical composition of groundwater are mainly controlled by the salinization process followed by cation-exchange reactions. The highly permeable aquifers at the east coastal region are characterized by low hydraulic gradient and discharge rate and high hydraulic conductivity as compared with other regions. These properties enhance the salinization of groundwater observed in the study area. Based on the Cl, Br, and δ¹⁸O data, seawater was determined to have intruded inland some 2.5 km from the coastline. Considering the poor correlation of sampling depth and Cl concentrations observed, the position of seawater-freshwater interface is not uniformly distributed in the study area, due to heterogeneities of the basaltic aquifers.