He,Sr and Nd isotopic variations in lavas from the juan fernandez archipelago,SE pacific

Helium, Sr, and Nd isotopic ratios and major and trace element compositions have been measured on a suite of lavas from the intra-plate volcanos of the Juan Fernandez Archipelago, Chile. Lavas from the islands of Mas Afuera and Mas a Tierra and from Monte Alpha and Friday seamounts have Sr and Nd isotopic ratios lying on the low¹⁴³Nd/¹⁴⁴Nd side of the mantle array (⁸⁷Sr/⁸⁶Sr:0.7034–0.7037;¹⁴³Nd/¹⁴⁴Nd:0.51281–0.51289). The homogeneity of these tracers suggests the involvement of a restricted range of mantle source compositions throughout Juan Fernandez volcanism. In marked contrast is the large range in³He/⁴He, from 7.8 to 18.0 R_A. A bimodal³He/⁴He distribution on Mas a Tierra is associated with two distinct volcanic lineages;³He/⁴He ratios of 14.5–18.0 R_A (n=15) occur in alkalic and tholeiitic shield basalts, whereas post-shield basanites range from 11.2 to 13.6 R_A (n=12). Elemental and isotopic systematics demonstrate a transition from an enriched (Loihi-like) plume source in the shield lavas to a more MORB-like source in the post-shield volcanics. The transition between these sources is much more pronounced in³He/⁴He than in the other isotopic tracers. The predominantly tholeiitic basalts of Mas Afuera have exceptionally uniform isotopic and elemental characteristics; Sr and Nd ratios are similar to those of Mas a Tierra, but³He/⁴He ratios are lower and more uniform at 8.3±0.5 R_A (n=17). The dramatic distinction between Mas Afuera and Mas a Tierra helium is surprising given the great similarity between the two islands in other geochemical characteristics. Both the Mas Afuera and Mas a Tierra results demonstrate that helium records systematic processes not readily apparent from other isotopic or elemental indicators. Neither magma chamber degassing nor local metasomatic events are likely to be responsible. We suggest that the observed variations may be attributed to mixing of plume and asthenospheric sources in which the plume component is characterized by a heterogeneous distribution of volatiles or has suffered extraction of small degree partial melts prior to mixing.     

Chemical and isotopic variations along the superfast spreading East Pacific Rise from 6 to 30°S

Chemical data of 39 fresh basaltic glasses from the East Pacific Rise (EPR) between 6 and 30°S and Pb, Sr, and Nd isotopic compositions of 12 basalt glasses are presented. Major and trace element data indicate a wide compositional range, including primitive basalts (Mg#=0.67) and highly evolved FeTi-basalts (Mg#=0.34) [molMg/(Mg+Fe²⁺)]. The compositional range can be attributed to low-pressure fractional crystallization. Fractionation-corrected major element concentrations provide evidence for varying mantle melting conditions. Calculations of the melting conditions suggest melt generation in a rising upper mantle column between 20 and 10 kbar, at temperatures between 1430 and 1280°C, and total degrees of partial melting between 17 and 20% by weight. Leached and hand-picked basalt glasses display large variations in ⁸⁷Sr/⁸⁶Sr (0.70235–0.70270), ¹⁴³Nd/¹⁴⁴Nd (0.51312–0.51323), and ²⁰⁶Pb/²⁰⁴Pb (18.064–18.665), but are similar to other N-type MORB from the EPR. The isotopic ratios of basalts from 13 to 23°S show strong correlations and delineate two systematic trends. From 23 to 17°S, ⁸⁷Sr/⁸⁶Sr and Pb isotope ratios increase and ¹⁴³Nd/¹⁴⁴Nd decrease in agreement with previous results (Mahoney et al. 1989). A reverse trend is indicated by basalts from 17 to 13°S. However, K/Ti and (La/Sm)_N continuously increase from 23 to 13°S. This opposite behavior indicates a recent decoupling of isotopic and minor element ratios in the mantle between 13 and 17°S. North of 13.5°S (Garrett Fracture Zone), isotopic data show no systematic variation with ridge location and display an overall weaker covariation. The results suggest that the isotopic variations and ridge segmentation appear to be unrelated and that major ridge offsets apparently coincide with changes in mantle melting conditions (P, T, F) (F, degrees of melting). There is no evidence for a systematic relationship between calculated melting conditions and second order ridge segmentation. Our isotopic data provide further evidence for regionally confined chemical variations in the mantle at 5 to 30°S. We interpret the isotopic trends as reflecting melting of distinct smallvolume and old enriched mantle components. In contrast, variations in trace elements are attributed to young mantle differentiation processes.     

Primitive and contaminated basalts from the Southern Rocky Mountains,U.S.A.

Basalts in the Southern Rocky Mountains province have been analyzed to determine if any of them are primitive. Alkali plagioclase xenocrysts armored with calcic plagioclase seem to be the best petrographic indicator of contamination. The next best indicator of contamination is quartz xenocrysts armored with clinopyroxene. On the rocks and the region studied, K₂O apparently is the only major element with promise of separating primitive basalt from contaminated basalt inasmuch as it constitutes more than 1 % in all the obviously contaminated basalts. K₂O: lead (> 4 ppm) and thorium (> 2 ppm) contents and Rb/Sr (> 0.035) are the most indicative of the trace elements studied. Using these criteria, three basalt samples are primitive (although one contains 1.7% K₂O) and are similar in traceelement contents to Hawaiian and Eastern Honshu, Japan, primitive basalts.Contamination causes lead isotope ratios, ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb, to become less radiogenic, but it has little or no effect on ⁸⁷Sr/⁸⁶Sr. We interpret the effect on lead isotopes to be due to assimilation either of lower crustal granitic rocks, which contain 5–10 times as much lead as basalt and which have been low in U/Pb and Th/Pb since Precambrian times, or of upper crustal Precambrian or Paleozoic rocks, which have lost much of their radiogenic lead because of heating prior to assimilation. The lack of definite effects on strontium isotopes may be due to the lesser strontium contents of granitic crustal rocks relative to basaltic rocks coupled with lack of a large radiogenic enrichment in the crustal rocks.Lead isotope ratios were found to be less radiogenic in plagioclase separates from an obviously contaminated basalt than in the primitive basalts. The feldspar separate that is rich in sodic plagioclase xenocrysts was found to be similar to the whole-rock composition for ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb whereas a more dense fraction probably enriched in more calcic plagioclase phenocrysts is more similar to the primitive basalts in lead isotope ratios.The primitive basalts have: ²⁰⁶Pb/²⁰⁴Pb 18.09–18.34, ²⁰⁷Pb/²⁰⁴Pb 15.5, ²⁰⁸Pb/²⁰⁴Pb 37.6–37.9, ⁸⁷Sr/⁸⁶Sr 0.704–0.705. In the primitive basalts from the Southern Rocky Mountains the values of ²⁰⁶Pb/²⁰⁴Pb are similar to values reported by others for Hawaiian and eastern Honshu basalts and abyssal basalts, whereas ²⁰⁸Pb/²⁰⁴Pb tends to be equal to or a little less radiogenic than those from the oceanic localities. ⁸⁷Sr/⁸⁶Sr appears to be equal to or a little greater than those of the oceanic localities. These ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios are distinctly less radiogenic and ⁸⁷Sr/⁸⁶Sr values are about equal to those reported by others for volcanic islands on oceanic ridges and rises.Publication authorized by the Director, U.S. Geological Survey     

He, Sr and Nd isotopes of mantle-derived xenoliths in volcanic rocks of NE China

Abundances and isotopic ratios of He and isotopic ratios of Sr and Nd have been measured for 18 mantle-derived xenoliths from three Cenozoic volcanic provinces in NE China. The xenoliths are characterized by low He concentrations (2.3×10⁻⁹–2.5×10⁻⁷ cm³ STP g⁻¹) and large variations of ³He/⁴He ratios (1.6×10⁻⁷–15.8×10⁻⁶ or R/Ra=0.1–11). ³He/⁴He, ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios in xenoliths from Kuandian Holocene volcanic provinces are consistent with those observed in mid-oceanic ridge basalt (MORB), indicating that the source of He–Sr–Nd in the lithospheric mantle is chemically and isotopically identical to that of MORB reservoir. However, xenoliths in Huinan Pleisteocene–Holocene volcanic province are characterized by slightly low ³He/⁴He ratios (R/Ra=4.3–6.5) and more radiogenic Sr and Nd. The age-corrected ³He/⁴He ratios suggest that their time-integrated ratio of (U+Th)/³He is slightly elevated compared to the depleted upper mantle. The Hannuoba xenoliths in the Miocene volcanic province show much lower and wider variable ³He/⁴He ratios, which is most likely caused by in situ radiogenic ⁴He accumulation since it erupted on to the surface. The He–Sr–Nd results suggest chemical and isotopical heterogeneity in the subcontinental mantle beneath NE China.     

Shear zone-related syenites in the Damara belt (Namibia): the role of crustal contamination and source composition

Geochemical and Nd-Sr-Pb-O isotope data for a suite of syn-collisional (ca. 520 Ma) syenites associated with a major shear zone in the Proterozoic Damara orogen (Namibia) constrain their sources and petrogenesis. Major rock types from within and outside the shear zone range from highly potassic nepheline syenites to quartz syenites and were primarily generated by fractional crystallization from a mantle-derived alkaline magma. Even the most primitive samples show pronounced depletion in Nb, Ti, Sr and P on a primitive mantle-normalized diagram, indicating the involvement of a recycled crustal component in the source. Extrapolation of the Sr-Nd-Pb-O isotope composition of the syenites from within the shear zone back to a hypothetical parental melt with 10 wt% MgO suggests derivation from a moderately enriched lithospheric upper mantle (⁸⁷Sr/⁸⁶Sr: 0.705, Nd: –2, ¹⁸O: 6, ²⁰⁶Pb/²⁰⁴Pb: 19.40, ²⁰⁷Pb/²⁰⁴Pb: 15.82). More evolved quartz syenites show increasing ⁸⁷Sr/⁸⁶Sr ratios, increasing ¹⁸O values but less radiogenic Nd values and Pb isotopes with decreasing MgO, indicating assimilation of ca. 10% Archaean to Proterozoic local lower crust with unradiogenic Nd, high ⁸⁷Sr/⁸⁶Sr and low U/Pb. For samples from outside the shear zone a hypothetical parental melt with 10 wt% MgO has distinctly more radiogenic Sr but less radiogenic Nd isotopic composition (⁸⁷Sr/⁸⁶Sr: 0.712, Nd: –13), with strongly unradiogenic Pb isotope ratios (²⁰⁶Pb/²⁰⁴Pb: 17.40, ²⁰⁷Pb/²⁰⁴Pb: 15.50), suggesting another strongly enriched lithospheric mantle source for these rocks. Differentiated syenites from outside the shear zone show decreasing ⁸⁷Sr/⁸⁶Sr, increasing ¹⁸O values, more radiogenic Nd values and Pb isotope ratios with decreasing MgO indicating interaction with a lithospheric component with low Rb/Sr but high Sm/Nd and U/Pb.     

Magma sources for Mesozoic anorogenic granites of the White Mountain magma series,New England,USA

The magma sources for granitic intrusions related to the Mesozoic White Mountain magma series in northern New England, USA, are addressed relying principally upon Nd isotopes. Many of these anorogenic complexes lack significant volumes of exposed mafic lithologies and have been suspected of representing crustal melts. Sm–Nd and Rb–Sr isotope systematics are used to evaluate magma sources for 18 felsic plutons with ages ranging from about 120 to 230 Ma. The possibility of crustal sources is further examined with analyses of representative older crust including Paleozoic granitoids which serve as probes of the lower crust in the region. Multiple samples from two representative intrusions are used to address intrapluton initial isotopic heterogeneities and document significant yet restricted variations (<1 in _Nd). Overall, Mesozoic granite plutons range in _Nd [T] from +4.2 to -2.3, with most +2 to 0, and in initial ⁸⁷Sr/⁸⁶Sr from 0.7031 to 0.709. The isotopic variations are roughly inversely correlated but are not obviously related to geologic, geographic, or age differences. Older igneous and metamorphic crust of the region has much lower Nd isotope ratios with the most radiogenic Paleozoic granitoid at _Nd [180 Ma] of -2.8. These data suggest mid-Proterozoic separation of the crust in central northern New England. Moreover, the bulk of the Mesozoic granites cannot be explained as crustal melts but must have large mantle components. The ranges of Nd and Sr isotopes are attributed to incorporation of crust by magmas derived from midly depleted mantle sources. Crustal input may reflect either magma mixing of crustal and mantle melts or crustal assimilation which is the favored interpretation. The results indicate production of anorogenic granites from mantle-derived mafic magmas.     

Trace-element and Sr,Nd, Pb,and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The cratonic basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in ⁸⁷Sr/⁸⁶Sr (0.70316 to 0.70512), ¹⁴³Nd/¹⁴⁴Nd (_Nd) and ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the cratonic basalts. In contrast, the transitional basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by ⁸⁷Sr/⁸⁶Sr=0.7039±0.0004, _Nd, ²⁰⁶Pb/²⁰⁴Pb=18.60±0.08, ²⁰⁷Pb/²⁰⁴Pb=15.60±0.01, and ²⁰⁸Pb/²⁰⁴Pb=38.50±0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the cratonic basalts, are displaced to higher ⁸⁷Sr/⁸⁶Sr at a given ¹⁴³Nd/¹⁴⁴Nd and to higher ²⁰⁷Pb/²⁰⁴Pb at a given ²⁰⁸Pb/²⁰⁴Pb. The transitional basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the cratonic and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ¹⁸O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ¹⁸O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ¹⁸O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc to back-arc volcanism in southern South America. The cratonic basalts do not contain the slab-derived components that impart the higher Ba/La, Ba/Nb, La/Nb, Cs/Rb, ⁸⁷Sr/⁸⁶Sr at a given ¹⁴³Nd/¹⁴⁴Nd, ²⁰⁷Pb/²⁰⁴Pb at a given ²⁰⁸Pb/²⁰⁴Pb, and ¹⁸O to Andean orogenic arc basalts. Instead, these basalts are formed by relatively low degrees of partial melting of heterogeneous lower continental lithosphere and/or asthenosphere, probably due to thermal and mechanical pertubation of the mantle in response to subduction of oceanic lithosphere below the western margin of the continent. The transitional basalts do contain components added to their source region by either (1) active input of slab-derived components in amounts smaller than the contribution to the mantle below the arc and/or with lower Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios than below the arc due to progressive downdip dehydration of the subducted slab; or (2) subarc source region contamination processes which affected the mantle source of the transitional basalts earlier in the Cenozoic.     

Geochemistry of Cretaceous mafic rocks from the Lower Yangtze region, eastern China: Characteristics and evolution of the lithospheric mantle

Geochemical and isotopic data for Cretaceous mafic rocks (basalt, gabbro, and diorite) from the Lower Yangtze region, northern Yangtze block, constrain the evolution of the lithospheric mantle. The mafic rocks, separated into the northeast and southwest groups, are alkaline and evolved, with low Mg# values (44–58) and variable SiO₂ contents (47.6–57.4 wt%). Enriched LREEs, LILEs, and Pb, together with depleted Nb, Zr, and Ti, suggest that the mantle sources were metasomatized by slab-derived fluid/melt. All samples show high radiogenic ²⁰⁷Pb/²⁰⁴Pb(t) (15.41–15.65) and ²⁰⁸Pb/²⁰⁴Pb(t) (37.66–38.51) ratios at given ²⁰⁶Pb/²⁰⁴Pb(t) (17.65–19.00) ratios, consistent with the mantle sources having been metasomatized by ancient slab-derived material. Mafic rocks of the southwest group show enriched Sr–Nd isotopic characteristics, with ⁸⁷Sr/⁸⁶Sr(t) ranging from 0.7056 to 0.7071 and ε_Nd(t) ranging from −5.3 to −8.3, indicating an origin from enriched lithospheric mantle. Mafic rocks of the northeast group, which record ⁸⁷Sr/⁸⁶Sr(t) ratios of between 0.7044 and 0.7050 and ε_Nd(t) of −2.8 to −0.7, possibly formed by the mixing of melts from isotopically enriched lithospheric mantle and isotopically depleted asthenospheric mantle. Taking into consideration the geochemical and isotopic characteristics of Cretaceous mafic rocks, Cenozoic basalts, and basalt-hosted peridotite xenoliths from the Lower Yangtze region, we propose that an isotopically enriched, subduction-modified lithospheric mantle was replaced by or transformed into an isotopically depleted “oceanic-type” mantle. Such a process appears to have occurred in the eastern North China Craton as well as the eastern Yangtze block, probably in response to subduction of the paleo-Pacific plate beneath East Asia.     

Geochemical variations in Andean basaltic and silicic lavas from the Villarrica-Lanin volcanic chain (39.5° S): an evaluation of source heterogeneity,fractional crystallization and crustal assimilation

At 39.5° S in the southern volcanic zone of the Andes three Pleistocene-recent stratovolcanoes, Villarrica, Quetrupillan and Lanin, form a trend perpendicular to the strike of the Andes, 275 to 325 km from the Peru-Chile trench. Basalts from Villarrica and Lanin are geochemically distinct; the latter have higher incompatible element abundances and La/Sm but lower Ba/La and alkali metal/La ratios. These differences are consistent with our previously proposed models involving: a) a west to east decrease in an alkali metal-rich, high Ba/La slab-derived component which causes an across strike decrease in degree of melting; or b) a west to east increase in the contamination of subduction-related magma by enriched subcontinental lithospheric mantle. Silicic and mafic lavas from the stratovolcanoes have overlapping Sr, Nd and O isotopic ratios. Silicic lavas also have geochemical differences that parallel those of their associated basalts, e.g., rhyolite from Villarrica has lower La/Sm and incompatible element contents than high-SiO₂ andesite from Lanin. At each volcano the most silicic lavas can be modelled by closed system fractional crystallization while andesites are best explained by magma mixing. Apparently crustal contamination was not an important process in deriving the evolved lavas. Basaltic flows from small scoria cones, 20–35 km from Villarrica volcano have high incompatible element contents and low Ba/La, like Lanin basalts, but trend to higher K/Rb (356–855) and lower ⁸⁷Sr/ ⁸⁶Sr (0.70361–0.70400) than basalts from either stratovolcano. However all basalts have similar Nd, Pb and O isotope ratios. The best explanation for the unique features of the cones is that the sources of SVZ magmas, e.g., slab-derived fluids or melts of the subcontinental lithospheric mantle, have varying alkali metal and radiogenic Sr contents. These heterogeneities are not manifested in stratovolcano basalts because of extensive subcrustal pooling and mixing. This model is preferable to one involving crustal contamination because it can account for variable Sr isotope ratios and uniform Nd and Pb isotope ratios among the basalts, and the divergence of the cones from across-strike geochemical trends defined by the stratovolcanoes.     

Isotopic relationships of volatile and lithophile trace elements in continental ultramafic xenoliths

The concentrations and isotopic compositions of Sr, Nd, Pb, He and C have been determined for suites of xenoliths from Bullenmerri (Australia), Ichinomegata (Japan), Geronimo (Arizona), and East Africa. The wehrlites and pyroxenites from Bullenmerri have Sr, Nd and Pb isotopic compositions that are generally similar to those found for alkali basalts in the region. The spinel lherzolites, in contrast, have higher ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb and lower ¹⁴³Nd/¹⁴⁴Nd ratios. Whereas the isotopic compositions of He are generally within the range of mid-ocean-ridge basalts (MORB) and do not covary with those of other trace elements, there is an apparent correlation between the ¹³C/¹²C and ¹⁴³Nd/¹⁴⁴Nd ratios for each of the two petrologic groups. These relationships, if substantiated for other xenolith suites, greatly limit the possible mechanisms for generating lithophile and volatile isotopic variations in the continental lithosphere. The helium isotopic compositions for all of the xenoliths fall within the range for MORB. This includes those from Ichinomegata, suggesting that the lower ³He/⁴He ratios found for He sampled at the surface at subduction zones result from mixing mantle He with near-surface crustal He rather than with subducted radiogenic He. Measured C isotopic compositions (relative to Peedee belemnite) for the Ichinomegata xenoliths include values that are both lighter and heavier than those in MORB, and are compatible with contributions from subducted carbon. The Nd and Sr isotopic compositions of the Ichinomegata xenoliths exhibit a correlation over a substantially greater range of values than typically observed for other light-rare-earth-element (LREE)-depleted xenoliths, and include more radiogenic Sr and less radiogenic Nd compositions. The carbon isotopic compositions found for the East African and Geronimo xenoliths extend to values that are lighter than those typically found for MORB.     

Permian basaltic rocks in the Tarim basin, NW China: Implications for plume–lithosphere interaction

There are large areas of Permian basaltic rocks in the Tarim basin (PBRT) in northwestern China. Precise Ar–Ar dating of these rocks revealed an eruption age span of 262 to 285 Ma. Most of the PBRT is composed of alkaline basaltic rocks with high TiO₂ (2.43%–4.59%, weight percent), high Fe₂O₃ + FeO (12.63%–17.83%) and P₂O₅ (0.32%–1.38%) contents. Trace elements of these rocks have affinities with oceanic island basalts (OIB), as shown in chondrite normalized rare earth elements (REE) diagrams and primitive mantle normalized incompatible elements diagrams. The rocks show complex Sr–Nd isotopic character based on which they can be subdivided into two distinct groups: group 1 has relatively small initial (t = 280 Ma)⁸⁷Sr/⁸⁶Sr ratio ( 0.7048) and positive εNd(t) (3.42–4.66) values. Group 2 has relatively large initial ⁸⁷Sr/⁸⁶Sr ratio (0.7060–0.7083) and negative εNd(t) (from − 2.79 to − 2.16) values. Lead isotopes are even more complex with variations of (²⁰⁶Pb/²⁰⁴Pb)t, (²⁰⁷Pb/²⁰⁴Pb)t and (²⁰⁸Pb/²⁰⁴Pb)t ranging from 17.9265 to 18.5778, 15.4789 to 15.6067 and 37.2922 to 38.1437, respectively. Moreover, these two groups have different trace elements ratios such as Nb/La, Ba/Nb, Zr/Nb, Nb/Ta and Zr/Hf, implying different magmatic processes. Based on the geochemistry of basaltic rocks and an evaluation of the tectonics, deformation, and the compositions of crust and lithospheric mantle in Tarim, we conclude that these basaltic rocks resulted from plume–lithosphere interaction. Permian mantle plume caused an upwelling of the Tarim lithosphere leading to melting of the asthenospheric mantle by decompression. The magma ascended rapidly to the base of lower crust, where different degrees of assimilation of OIB-like materials and fractionation occurred. Group 1 rocks formed where the upwelling is most pronounced and the assimilation was negligible. In other places, different degrees of assimilation and fractionation account for the geochemical traits of group 2.     

Basalt-rhyolite volcanism by MORB-continental crust interaction: Nd,Sr-isotopic and geochemical evidence from southern San Joaquin Basin,California

The early miocene Tecuya volcanic center in the southern San Joaquin basin of California consists of flows and tuffs of basalt and rhyolite that erupted, closely spaced in time, in both submarine and subaerial conditions. The rhyolites are overlain by the basalts and constitute approximately 45% of a total of at least 180 km³ of the Tecuya volcanic rocks. The basalts have _Nd(t) values of +2 to +6 and (⁸⁷Sr/⁸⁶Sr)_i values between 0.7035 and 0.7052. These rocks show LREE enrichment [(La/Yb)_N =2.4–5.5; La=28–150 times chondrite] and higher Th/U, Th/Ta, Rb/Ta, Ba/Ta, Cs/Rb but lower K/Rb ratios than MORB. Combined major- and trace-element, and Sr–Nd isotopic data suggest the involvement of subcontinental lithosphere, depleted upper mantle source (MORB), and local continental crust in the basalt petrogenesis. _Nd(t) values in rhyolites vary from +1.5 to +3.7 while (⁸⁷Sr/⁸⁶Sr)_i ratios range from 0.7051 to 0.7064. The rhyolites display LREE enrichment [(La/Yb)_N=10; La=100 times chondrite] along with a distinct negative Eu anomaly (Eu/Eu^*=0.75) and depletion of Ti and P. Mixing relations in (⁸⁷/⁸⁶Sr)_i – _Nd(t) space among basalts, rhyolites, and local continental crust indicate that the Tecuya rhyolites were produced by assimilation of variable amounts of continental crust by MORB-related magmas and subcontinental lithosphere-derived melts. This conclusion is supported by the synchroneity of Tecuya volcanism at 22 Ma with interaction of a segment of the East Pacific Rise along the southern California margin. The Tecuya volcanic rocks thus provide an example for the generation of rhyolitic melts owing to crustal assimilation by basaltic melts during mid-oceanic ridge-induced magmatism along a continental margin.     

Pb,Sr and 10Be isotopic studies of volcanic rocks from the Northern Mariana Islands. Implications for magma genesis and crustal recycling in the Western Pacific

We report Sr and Pb isotope analyses for an extensive suite of volcanic rocks from the N. Mariana arc together with Sr and Pb isotope analyses of sediments from the nearby Mariana and Nauru basins. In addition ten of the most recent volcanic samples were analysed for ¹⁰Be.The Sr isotope compositions cluster tightly around ${}^{87}\text{Sr}{}^{86}\text{Sr}$ = 0.7035 being slightly but significantly higher than the Pacific ocean floor basalts on either side of the arc and agreeing well with previous data. In contrast, the large number of new Pb isotopic data presented significantly extends the observed range of Pb isotope compositions for volcanic rocks from the Mariana arc to more radiogenic compositions. The concentrations of ¹⁰Be were very low (< 0.5 × 10⁶ atom g^?1).These new data require either that the Pb and Sr isotopic compositions of the Mariana sub-arc mantle be substantially different from those of the mantle source of ocean floor basalts on either side of the arc, or that the enrichment in radiogenic Pb and Sr relative to the values observed in Pacific ocean floor basalts be related to the subduction process. We prefer the latter hypothesis in which radiogenic Sr and Pb in ocean floor sediments are added to M.O.R.B. type mantle either by direct assimilation of the sediments in partial melts or, more probably, by transfer in a fluid phase into the zone of magma production. The low ¹⁰Be concentrations observed suggest the removal of at least the top few metres of sediment during subduction.     

Isotope and trace element evidence for three component mixing in the genesis of the North Luzon arc lavas (Philippines)

Post-3Ma volcanics from the N Luzon arc exhibit systematic variations in ⁸⁷Sr/⁸⁶Sr (0.70327–0.70610), ¹⁴³Nd/¹⁴⁴Nd (0.51302–0.51229) and ²⁰⁸Pb^*/²⁰⁶Pb^* (0.981–1.035) along the arc over a distance of about 500 km. Sediments from the South China Sea west of the Manila Trench also exhibit striking latitudinal variations in radiogenic isotope ratios, and much of the isotopic range in the volcanics is attributed to variations in the sediment added to the mantle wedge during subduction. However, Pb-Pb isotope plots reveal that prior to subduction, the mantle end-member had high 8/4, and to a lesser extent high 7/4, similar to that in MORB from the Indian Ocean and the Philippine Sea Plate. Th isotope data on selected Holocene lavas indicate a source with unusually high Th/U ratios (4.5–5.5). Combined trace element and isotope data require that three end-members were implicated in the genesis of the N Luzon lavas: (1) a mantle wedge end-member with a Dupal-type Pb isotope signature, (2) a high LIL/HFS subduction component interpreted to be a slab-derived hydrous fluid, and (3) an isotopically enriched end-member which reflects bulk addition (<5%) of subducted S China Sea terrigenous sediment. The ⁸⁷Sr/⁸⁶Sr ratios in the volcanics show a restricted range compared with that in the sediments, and this contrasts with ¹⁴³Nd/¹⁴⁴Nd and ²⁰⁸Pb^*/²⁰⁶Pb^*, both of which have similar ranges in the volcanics and sediments. Such differences imply that whereas the isotope ratios of Nd, Pb and Th are dominated by the component from subducted sediment, those of Sr reflect a larger relative contribution from the slab-derived fluid.     

Geochemical and Sr-Nd-Pb isotopic characteristics of Late Cenozoic leucite lamproites from the East European Alpine belt (Macedonia and Yugoslavia)

In the East European Alpine belt, leucite-sanidine-phlogopite-olivine-bearing volcanic rocks of Late Cenozoic age occur at eight localities within the Vardar suture zone and at one locality in the Southern Carpathian fold-and-thrust belt. Most of these volcanics are characterized by high Mg# (66.6–78.6), high abundances of Ni (117–373 ppm) and Cr (144–445 ppm) as well as high primary K₂O contents (5.63–7.01 %) and K₂O/Na₂O values (1.93–4.91). Rocks with more differentiated compositions are rare. A lamproite affinity of these rocks is apparent from their relatively low contents of Al₂O₃ (9.9–14.3 wt%) and CaO (6.2–8.3 wt%) in combination with high abundances of Rb (85–967 ppm), Ba (1,027–4,189 ppm), Th (18.9–76.5 ppm), Pb (19–54 ppm), Sr (774–1,712 ppm) and F (0.16–0.52 wt%), and the general lack of plagioclase. Although eruption of the magmas took place in post-collisional extensional settings, significant depletions of Nb and Ta relative to Th and La, low TiO₂ contents (0.92–2.17 %), low ratios of Rb/Cs, K/Rb and Ce/Pb as well as high ratios of Ba/La and Ba/Th suggest close genetic relationships to subduction zone processes. Whereas Sr and Nd isotope ratios show relatively large variations (⁸⁷Sr/⁸⁶Sr = 0.7078–0.7105, ¹⁴³Nd/¹⁴⁴Nd = 0.51242–0.51215), Pb isotope ratios display a very restricted range with ²⁰⁶Pb/²⁰⁴Pb = 18.68–18.88 and variable but generally high 7/4 (11–18) and 8/4 (65–95) values. The observed petrographic, geochemical and isotopic characteristics are best explained by a genetic model involving preferential melting of phlogopite-rich veins in an originally depleted lithospheric mantle source, whereby the metasomatic enrichment of the mantle source is tentatively related to the addition of components from subducted sediments during consumption of Tethyan oceanic lithosphere.Editorial responsibility: J. Hoefs     

Elemental and isotopic variations in subduction related basalts: evidence for a three component model

Subduction related basalts display wide ranges in large ion lithophile element ratios (e.g., Rb/Ba and Rb/ Sr) which are unlikely to result from mixing, but suggest a role for small degree partial melting of a relatively Rb-poor mantle wedge source. However, these variations do not correlate with other trace element criteria, such as the depletions of high field strength elements (HFSE) and light rare earth elements (LREE) relative to the LILE, which characterise subduction related magmatism. Integration of radiogenic isotope and trace element data demonstrates that the elemental enrichment cannot be simply related to two component mixtures inferred from isotopic variations. Thus a minimum of three components is required to describe the geochemistry of subduction zone basalts. Two are subduction related: high Sr/Nd material is derived from the dehydration of subducted basaltic ocean crust, and a low Sr/Nd component is thought to be from subducted terrigenous sediment. The third component is in the mantle wedge, it is usually similar to the source of MORB, particularly in its isotopic composition. However, in some cases, notably continental areas, more enriched mantle wedge material with relatively high ⁸⁷Sr/⁸⁶Sr, low ¹⁴³Nd/¹⁴⁴Nd and elevated incompatible trace element contents may be involved Mixing of these three components is capable of producing both the entire range of Sr, Nd and Pb isotope signatures observed in destructive margin basalts, and their distinctive trace element compositions. The isotope differences between Atlantic and Pacific island arc basalts are attributed to the isotope compositions of sediments in the two oceans.     

He,Ne, Ar,and C isotope systematics of geothermal emanations in the Lesser Antilles Islands Arc

We present He, Ne, Ar, and C isotope analyses of hydrothermal brines and gases from fumaroles, hot springs, mofettes and hydrothermal exploration drillings on the major islands of the Lesser Antilles Arc. The origin of hydrothermal brines, which have been analyzed also for O and H isotopes, is essentially meteoric-hydrothermal. Air-corrected isotope compositions of helium (2.2 Rc/Ra < ³He/⁴He < 8.6 Rc/Ra) and carbon (−20 < δ¹³C_PDB < +0.5) are variable and require a variety of crustal and magmatic sources. The diversity of δ¹³C_PDB and ³He/CO₂ ratios within individual volcanic centres suggests that crustal sources (e.g., limestone) contaminate magmatic CO₂ en route from high-level magma reservoirs (depth < 15 km) to the surface. A similar contamination may be found for magmatic helium on distal springs. The ³He/⁴He signature of summit fumaroles, thought to reflect the ³He/⁴He signature of high-level magmas, shows a remarkable systematic variation along the arc. In addition, there is a correlation throughout the arc between published Sr, Pb, and Nd isotope signatures of lavas and the ³He/⁴He signatures of summit fumaroles. On the northern islands (Nevis, Montserrat, Guadeloupe, and Dominica) summit fumaroles have the N-MORB signature (³He/⁴He = 8 ± 1 R/Ra), and the isotope signature of lavas is not dissimilar from comparable intra-oceanic arc tholeiites elsewhere. Variable enrichments in radiogenic Sr and Pb have been reported for lavas of individual volcanic centres of the Southern Islands (Martinique, St.Lucia, and Grenada), and summit fumaroles on these centres match these variations by variable radiogenic He-enrichments, i.e., lower ³He/⁴He ratios. This correlation suggests that radiogenic Sr and Pb enrichments of lavas and low ³He/⁴He signatures on summit fumaroles have a common origin, i.e., a terrigenous contaminant derived from the Orinoco depositionary fan. Crustal assimilation is thought to decouple the He isotope system from any other radiogenic isotope system and, therefore, we argue that the observed correlation of He, Sr, Pb, and Nd isotope systems is related to a terrigenous contaminant derived from subducted sediments. Support for this scenario also comes from the matching of low ³He/⁴He ratios and tectonic features of the forearc thought to favor the subduction of forearc sediments.The present study offers a first clue that, under suitable conditions, crustal helium from oceanic sediments might be subducted to the depth of arc magma sources and, possibly, even recycled into the deeper mantle.     

Origin of Sr,Nd and Pb isotopic systematics in high-Sr basalts from central Arizona

Alkalic and tholeiitic basalts were erupted in the central Arizona Transition Zone during Miocene-Pliocene time before and after regional faulting. The alkalic lava types differ from the subalkaline lavas in Sr, Nd and Pb isotopic ratios and trace element ratios and, despite close temporal and spatial relationships, the two types appear to be from discrete mantle sources. Pre-faulting lava types include: potassic trachybasalts (⁸⁷Sr/⁸⁶Sr = 0.7052 to 0.7055, _Nd= –9.2 to –10.7); alkali olivine basalts (⁸⁷Sr/ ⁸⁶Sr = 0.7049 to 0.7054, _Nd= –2 to 0.2); basanite and hawaiites (⁸⁷Sr/⁸⁶Sr = 0.7049 to 0.7053, _Nd= –3.5 to –7.8); and quartz tholeiites (⁸⁷Sr/⁸⁶Sr = 0.7047, _Nd= –1.4 to –2.6). Post-faulting lavas have lower ⁸⁷Sr/⁸⁶Sr (<0.7045) and _Nd from –3.2 to 2.3. Pb isotopic data for both preand post-faulting lavas form coherent clusters by magma type with values higher than those associated with MORB but within the range of values found for crustal rocks and sulfide ores in Arizona and New Mexico. Pb isotopic systematics appear to be dominated by crustal contamination. Effects of assimilation and fractional crystallization are inadequate to produce the Sr isotopic variations unless very large amounts of assimilation occurred relative to fractionation. It is impossible to produce the Nd isotopic variations unless ancient very unradiogenic material exists beneath the region. Moreover the assumption that the alkalic lavas are cogenetic requires high degrees of fractionation inconsistent with major- and trace-element data. Metasomatism of the subcontinental lithosphere above a subduction zone by a slab-derived fluid enriched in Sr, Ba, P and K could have produced the isotopic and elemental patterns. The degree of metasomatism apparently decreased upward, with the alkalic lavas sampling more modified regions of the mantle than the tholeiitic lavas. Such metasomatism may have been a regional event associated with crustal formation at about 1.6 Ga. Disruption and weakening of the subcontinental lithosphere in the Transition Zone of the Colorado Plateau by volcanism probably made deformation possible.     

Pb and Sr systematics of ultrapotassic and basaltic rocks from the central Sierra Nevada,California

This study presents Sr and Pb isotopic ratios and Rb, Sr, U, Th, and Pb concentrations of an ultrapotassic basaltic suite and related rocks from the central Sierra Nevada, California. The ultrapotassic suite yields a narrow range of Sr and Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr=0.70597–0.70653; ²⁰⁶Pb/ ²⁰⁴Pb=18.862–19.018; ²⁰⁷Pb/²⁰⁴Pb=15.640–15.686; ²⁰⁸Pb/ ²⁰⁴Pb=38.833–38.950). Associated basalts containing ultramafic nodules have less radiogenic Sr (⁸⁷Sr/⁸⁶=0.70430–0.70521) and generally higher Rb/Sr ratios than the ultrapotassic suite. Leucitites from Deep Springs Valley, California, contain high ⁸⁷Sr/⁸⁶Sr (71141–0.71240) and low ²⁰⁶Pb/²⁰⁴Pb (17.169–17.234) ratios, reflecting contamination by crustal granulite.The isotopic relationships support an origin of the ultrapotassic basaltic suite by partial melting of an enriched upper mantle source. Dehydration of a gently inclined oceanic slab beneath the Sierra Nevada may have provided Ba, K, Rb, Sr, and H₂O, which migrated into the overlying upper mantle lithosphere. The end of subduction 10 m.y. ago allowed increased asthenospheric heat flow into the upper mantle lithosphere. The increased heat flow enhanced fluid movement in the upper mantle and contributed towards isotopic homogenization of the upper mantle source areas. Continued heating of the enriched upper mantle caused partial melting and subsequent eruption of the ultrapotassic lavas.     

Petrogenesis of isotopically unusual Pliocene olivine leucitites from Deep Springs Valley, California

High-K mafic alkalic lavas (5.4 to 3.2 wt% K₂O) from Deep Springs Valley, California define good correlations of increasing incompatible element (e.g., Sr, Zr, Ba, LREE) and compatible element contents (e.g., Ni, Cr) with increasing MgO. Strontium and Nd isotope compositions are also correlated with MgO; ⁸⁷Sr/⁸⁶Sr ratios decrease and ɛ_Nd values increase with decreasing MgO. The Sr and Nd isotope compositions of these lavas are extreme compared to most other continental and oceanic rocks; ⁸⁷Sr/⁸⁶Sr ratios range from 0.7121 to 0.7105 and ɛ_Nd values range from −16.9 to −15.4. Lead isotope ratios are relatively constant, ²⁰⁶Pb/²⁰⁴Pb ∼17.2, ²⁰⁷Pb/²⁰⁴Pb ∼15.5, and ²⁰⁸Pb/²⁰⁴Pb ∼38.6. Depleted mantle model ages calculated using Sr and Nd isotopes imply that the reservoir these lavas were derived from has been distinct from the depleted mantle reservoir since the early Proterozoic. The Sr-Nd-Pb isotope variations of the Deep Springs Valley lavas are unique because they do not plot along either the EM I or EM II arrays. For example, most basalts that have low ɛ_Nd values and unradiogenic ²⁰⁶Pb/²⁰⁴Pb ratios have relatively low ⁸⁷Sr/⁸⁶Sr ratios (the EM I array), whereas basalts with low ɛ_Nd values and high ⁸⁷Sr/⁸⁶Sr ratios have radiogenic ²⁰⁶Pb/²⁰⁴Pb ratios (the EM II array). High-K lavas from Deep Springs Valley have EM II-like Sr and Nd isotope compositions, but EM I-like Pb isotope compositions. A simple method for producing the range of isotopic and major- and trace-element variations in the Deep Springs Valley lavas is by two-component mixing between this unusual K-rich mantle source and a more typical depleted mantle basalt. We favor passage of MORB-like magmas that partially fused and were contaminated by potassic magmas derived from melting high-K mantle veins that were stored in the lithospheric mantle. The origin of the anomalously high ⁸⁷Sr/⁸⁶Sr and ²⁰⁸Pb/²⁰⁴Pb ratios and low ɛ_Nd values and ²⁰⁶Pb/²⁰⁴Pb ratios requires addition of an old component with high Rb/Sr and Th/Pb ratios but low Sm/Nd and U/Pb ratios into the mantle source region from which these basalts were derived. This old component may be sediments that were introduced into the mantle, either during Proterozoic subduction, or by foundering of Proterozoic age crust into the mantle at some time prior to eruption of the lavas. Received: 28 February 1997 / Accepted: 9 July 1998