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.     

Sr and Pb isotopes,U and Th chemistry of the alkaline Monteregian and White Mountain igneous provinces,eastern North America

The Monteregian Hills and younger White Mountain alkaline intrusions were emplaced into the Cambro-Ordovician sediments of the St. Lawrence Lowlands and the folded and thrusted Lower Paleozoic sequence of the Appalachian orogen. Age relations indicate that there is a fine-scale structure to the igneous activity, with slightly undersaturated to critically saturated rocks emplaced between 141 and 128 Ma and strongly undersaturated rocks emplaced between 121 and 117 Ma.Sr and Pb isotopic data for the mantle-derived alkali picrite, alkali olivine basalt and basanite magmas, indicate derivation from a depleted mantle similar to that which produces present-day oceanic island basalts. For the most isotopically primitive samples, decay-corrected ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{= 0.7030–0.7037}$, ${}^{206}\text{Pb}{}^{204}\text{Pb}\text{= 19.05–19.72}$, ${}^{207}\text{Pb}{}^{204}\text{Pb}\text{= 15.56–15.65}$, and ${}^{208}\text{Pb}{}^{204}\text{Pb}\text{= 38.64–39.26}$. On Pb-Sr isotope correlation diagrams the data define trends similar to those for MOR basalts, implying mantle heterogeneity which requires the presence of a component enriched in radiogenic Pb relative to Sr. The interaction of these isotopically primitive magmas with the crust can be defined in terms of a three component system: depleted mantle-Grenville age crust-Lower Paleozoic age crust. The granitic magmas were apparently derived from the Lower Paleozoic crust of the Appalachian orogen.For the mantle-derived magmas, Th/U ratios vary from 2.5 (estimated ratio for MORB source) to 5.1, with the mean value near that of the bulk earth. The variations in Th/U suggest mantle heterogeneity on a local scale, and the high Th/U of some samples suggests that the mantle was enriched in incompatible elements shortly before melting. The magmas derived by partial melting of the crust have Th/U of 3.3 to 8.7, and the higher ratios are associated with rocks crystallized from magmas that originated by melting of Lower Paleozoic sediments.The Sr and Pb isotopic data support the conclusion of Bellet al. (1982) that the subcontinental mantle under eastern Canada underwent a Precambrian depletion event. This depleted mantle apparently extends under the White Mountain province and is isotopically similar to the mantle which gives rise to oceanic island basalts. In contrast, Pb isotopic ratios for the New England Seamount chain (TARAS and HART, 1983), which apparently represents the oceanic extension of this magmatic activity, are significantly more radiogenic. It is possible that a mantle plume provided the heat energy, and perhaps metasomatic fluids, to trigger melting in the subcontinental mantle, whereas in the case of the oceanic extension the plume directly contributed to the observed magmatism, as reflected in the more radiogenic Pb ratios.     

Strontium isotopic studies of the volcanic rocks of the Saunda arc,Indonesia, and their petrogenetic implications

Pleistocene and Recent lavas from the Sunda arc range from those showing affinities with the island arc tholeiitic series, through a spectrum of calc-alkaline to high-K alkaline rocks. The tholeiitic rocks have relatively low ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios averaging 0–7043; the calc-alkaline rocks show a wide range (from 0.7038 to 0.7059, averaging 0.7048); the high-K alkaline rocks average 0.7045. A rhyolitic ignimbrite from Sumatra has an ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio of 0.7139.The relationship between ${}^{87}\text{Sr}{}^{86}\text{Sr}$ and major and trace element geochemistry is variable and complex. Lavas from the same volcano sometimes show significant differences in ${}^{87}\text{Sr}{}^{86}\text{Sr}$ despite close geochemical relationships. Rocks of the calc-alkaline suite show a regular decrease in ${}^{87}\text{Sr}{}^{86}\text{Sr}$ from West Java to Bali and there is some evidence for increasing ${}^{87}\text{Sr}{}^{86}\text{Sr}$ with increasing depth to the Benioff zone. Calc-alkaline and tholeiitic rocks from the Sunda arc have significantly higher ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios than those from other island arcs, except from those arcs where continental crustal involvement has been inferred (e.g. New Zealand).A model of ⁸⁷Sr enrichment due to isotopic equilibration of oceanic crust with sea water and disequilibrium melting in the slab and/or mantle is favoured to explain the Sr isotopic composition of the tholeiitic and normal calc-alkaline lavas. Calc-alkaline lavas with high ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios are best explained by either sialic contamination, or the presence of alkali basalt as a component of the downgoing slab. The Sr isotopic data for the high-K alkaline lavas suggest a mantle origin. The high ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio in the Lake Toba rhyolite implies a crustal origin.     

Strontium isotope geochemistry of Icelandic geothermal systems and implications for sea water chemistry

Chemical and Sr isotopic analyses have been made of waters from 16 geothermal sites in Iceland with particular reference to the systems at Reykjanes and Svartsengi for which compositions of geothermal sea water and fresh and hydrothermally-altered rocks have been compared. The alkalies display mixing relationships indicating a hydrothermal input of Rb and K to local meteoric and sea waters as do results for Sr and Ca involving high-temperature fluids. ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios of the geothermal waters of meteoric origin parallel those of associated rocks but are higher. Ratios for geothermal sea waters are 0.7042 (Reykjanes) and 0.7040 (Svartsengi), lower than for normal sea water (0.7092) because of leaching of Sr from rocks followed by partial removal into alteration minerals, of which epidote and chlorite may be most important. Consequently, associated hydrothermally-altered rocks have been subject to significant Sr isotopic contamination by sea water Sr raising ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios from 0.7032 for fresh rock to 0.7038–0.7042 (Reykjanes) and to 0.7039–0.7041 (Svartsengi). Altered basalt is only ~50% equilibrated isotopically with geothermal sea water, at a water/rock ratio of ~2, but is internally equilibrated whereas palagonitized rocks (water/rock ratio of 3 to 4) are close to Sr isotopic equilibrium with associated sea water but show significant internal Sr disequilibrium. Hydrothermal input is unlikely to be important in the oceanic mass balance of Sr but is likely to be highly significant in controlling the strontium isotopic composition of sea water.     

Isotopic and incompatible element constraints on the genesis of island arc volcanics from Cold Bay and Amak Island,Aleutians, and implications for mantle structure

Cold Bay and Amak Island, two Quaternary volcanic centers in the eastern Aleutians, are orthogonal relative to the trench and separated by ~50 km. Sr, Nd and Pb isotopic compositions of the calc-alkaline andesite magmas show no sign of contamination from continental crust (average ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{= 0.70323}$, ${}^{143}\text{Nd}{}^{144}\text{Nd}\text{= 0.51301}$, ${}^{206}\text{Pb}{}^{204}\text{Pb}\text{= 18.82}$, ${}^{207}\text{Pb}{}^{204}\text{Pb}\text{= 15.571}$). These samples plot within the mantle arrays for Sr-Nd and for Pb and are similar to arcs such as the Marianas and New Britain (Sr-Nd) and Marianas and Tonga (Pb). Incompatible element ratios for the Aleutian andesites (K/Rb ~ 332, K/Cs ~ 10,600, K/Sr ~ 22.4, K/Ba ~ 18.3, Ba/La ~ 60) are within the range reported for arc basalts, despite the difference in degree of fractionation.Average K content, K/Rb, K/Ba and K/Sr are approximately the same for basalts from arcs and from oceanic islands (OIB); K/Cs is a factor of 4 lower and Ba/La almost 3 times higher in arcs. Abundance ratio correlations indicate that arcs are enriched in Cs and depleted in La relative to OIB, with other incompatible element abundances very similar. Histograms of Sr and Nd isotopic compositions for MORB, OIB, and intraoceanic arcs show remarkably similar peaks and distribution patterns for intraoceanic arcs and OIB.A “plum pudding” model for the upper mantle best accommodates a) geochemical coherence of OIB and IAV, b) the existence of mantle plumes at some oceanic islands, and c) the presence of a MORB-type source at back arc spreading centers. In this model, OIB plums are imbedded in a MORB matrix; small degrees of melting generate OIB-type magmas while larger degrees of melting dilute the OIB magma with MORB matrix melts.OIB plums are merely less robust lower mantle plumes (i.e., blobs) which are distributed throughout the upper mantle by convection. The existence of at least two types of OIB, as indicated by Sr, Nd, and Pb isotopes, suggests that nuggets of recycled oceanic lithosphère may coexist with lower-mantle plums and that both may be tapped in arcs and intraplate environments.     

A detailed Pb isotopic study of crustal contamination/assimilation: The Edgecumbe volcanic field,SE Alaska

To better understand the process of crustal contamination/assimilation, 23 Pb isotopic compositions and 12 concentrations have been measured on lavas and basement rocks from the Edgecumbe volcanic field, SE Alaska. Measured isotopic ratios have the following ranges: ${}^{206}\text{Pb}{}^{204}\text{Pb}\text{= 18.477–19.161}$; ${}^{207}\text{Pb}{}^{204}\text{Pb}\text{= 15.562–15.679}$; ${}^{208}\text{Pb}{}^{204}\text{Pb}\text{= 38.17–38.85}$. While the data form well-constrained linear arrays on Pb-Pb diagrams, no simple correlation exists with major element composition. Basaltic lavas (≤ 51 wt% SiO₂) are characterized by two isotopic groups. The olivine basalt (≤ 48% SiO₂) is more radiogenic than the plagioclase basalt (48–51%) which also shows more heterogeneity. In the silica range 52–55%, Pb isotopic ratios increase significantly but remain fairly constant in the range 55–70% SiO₂. Lead concentrations vary from 1 ppm in the basalts to 7 ppm in the rhyodacites. Analyzed basement rocks are more radiogenic than any of the lavas $\text{(}{}^{206}\text{Pb}{}^{204}\text{Pb}\text{= 19.20}$; ${}^{207}\text{Pb}{}^{204}\text{Pb}\text{= 15.65}$; ${}^{208}\text{Pb}{}^{204}\text{Pb}\text{= 38.86}$. The Pb isotopic data are qualitatively consistent with the contamination process described by Myerset al. (1984). However, because of fundamental differences in the mixing relations between the Sr system studied earlier and the Pb system, the new Pb data have revealed details of the process not apparent from the Sr data alone. In particular, it has been shown that the parent magma was more primitive than originally assumed, and that two contamination events are recorded in the lavas. The first event, involving a mafic parent and different crustal contaminants, produced the intermediate and siliceous hybrids in cupolas located above the main basaltic chamber. The types of country rock intruded as well as the degree of partial fusion achieved in individual cupolas controlled the range of hybrid compositions produced while the eruption sequence was determined by the order in which the cupolas were tapped. The second contamination event produced the plagioclase basalt, the most voluminous basaltic unit, by mixing the mafic parent with the olivine basalt, an independent, primary magma. Our results suggest crustal contamination models that assume bulk assimilation of crustal end members may be too simplistic.     

Chemical and isotopic evidence for mixing between depleted and enriched mantle,northwestern U.S.A.

Combined elemental and Sr, Nd, Pb and O isotopic data for late Cenozoic olivine tholeiite lavas from the northwestern Great Basin indicate derivation from at least two chemically and isotopically distinct mantle source regions with no significant modification by interaction with continental crust. The lack of crustal involvement is a direct reflection of the extensional tectonic environment which favors rapid ascent of magmas, minimal residence time in crustal magma chambers and scattered fissure eruptions.The observed chemical and isotopic variations in the tholeiite suite are attributed to mixing between depleted oceanic type mantle (${}^{87}\text{Sr}{}^{86}\text{Sr}\text{~ 0.7030}$ and ${}^{143}\text{Nd}{}^{144}\text{Nd}\text{~ 0.51305}$) and old, chemically heterogeneous, isotopically enriched subcontinental mantle (${}^{87}\text{Sr}{}^{86}\text{Sr}\text{~ 0.7078}$ and ${}^{143}\text{Nd}{}^{144}\text{Nd}\text{~ 0.51233}$). Model incompatible element concentrations suggest strong similarities between the depleted mantle and the mantles beneath normal oceanic ridge segments and back-arc basins and between the enriched mantle and the mantle beneath enriched oceanic ridge segments such as the Azores. Superimposed upon the characteristics derived from the two component mixing model may be the effects of a third mantle source which is identifiable only by its apparent radiogenic ${}^{206}\text{Pb}{}^{204}\text{Pb}$ ratios. If present, this third source may reflect a component derived from the downgoing slab of an ancient subduction zone.     

Lead isotope systematics of some igneous rocks from the Egyptian shield

Lead isotope data on late Precambrian igneous rocks from the eastern desert of Egypt are presented. Previous work has indicated that this igneous suite is characterized by uniformly low initial ratios of ${}^{37}\text{Sr}{}^{86}\text{Sr}$ (< 0.7035). The Pb data define three groups, loosely corresponding to age. An older tonalite to granodiorite (OTG) suite, with ages in the range 610–710 Ma, has Pb isotope characteristics similar to modern, mantle-derived oceanic mafic rocks. The age-corrected initial Pb isotope ratios of the OTG group lie near the “ocean regression line” in correlation diagrams of ${}^{206}\text{Pb}{}^{204}\text{Pb}$ vs. ${}^{207}\text{Pb}{}^{204}\text{Pb}$ and ${}^{203}\text{Pb}{}^{204}\text{Pb}$. The isotope data imply an origin for the OTG group analogous to calc-alkalic igneous rocks in modern intra-oceanic island arcs.A younger suite of K-rich plutonic rocks (570–595 Ma) has similar ${}^{206}\text{Pb}{}^{204}\text{Pb}$ and ${}^{208}\text{Pb}{}^{204}\text{Pb}$ initial ratios relative to the OTG suite, but have higher ${}^{207}\text{Pb}{}^{204}\text{Pb}$ initial ratios when calculated from measured whole-rock U and Pb contents. However, K-feldspar and galena, associated with this suite, indicate initial Pb isotope ratios close to the OTG suite. We interpret this to indicate that the younger granites could have originated by anatexis of OTG-type material, but they probably experienced an episode of metasomatism after emplacement.A suite of volcanic rocks (the Dokhan Volcanics) from the central eastern desert are intermediate between the younger granites and OTG in both age (～ 610 Ma) and Pb isotope characteristics.Limited data on initial ${}^{208}\text{Pb}{}^{204}\text{Pb}$ ratios suggest that all the Egyptian samples originated from a source with anomalously low $\text{Th}\text{Pb}$ ratios.Although the relative abundance of granitic rocks in the Egyptian Shield decreases to the south, no evidence of north-south heterogeneity in the Pb isotope composition of the respective source regions is apparent in the data. However, the westernmost sample studied, from the Aswan area, contains distinctly more radiogenic Pb relative to the mean. This location may mark the boundary between the Late Precambrian ensimatic orogen now outcropping in the Egyptian and Saudi Arabian Shields, and an older sialic craton to the west.     

The Archaean Marda igneous complex,Western Australia

The Marda complex is a sequence of andesitic to dacitic to rhyolitic volcanic rocks filling a synformal structure in submarine basalt, banded iron-formation and siliceous sediments in the Archaean Yilgarn Block of Western Australia. The Marda volcanic rocks are in part subaerial and exhibit calc-alkaline chemistry. Their Rb/Sr age is 2635 ± 80 m.y. with an initial $\text{Sr}{}^{87}\text{Sr}{}^{86}$ ratio of 0.7029 ± 0.0015. The Marda lavas represent products of a differentiated late to syn-tectonic, anatectic magma derived from the base of the Archaean crust. Calc-alkaline volcanic complexes are uncommon in the Yilgarn Block.     

Sr and Nd isotopic evidence for petrogenesis of mid-tertiary felsic volcanism in the mineral district of Zacatecas,Zac. (Sierra Madre Occidental), Mexico

Twelve samples of mid-Tertiary felsic volcanic rocks from Zacatecas and San Luis Potosí (both belonging to the Sierra Madre Occidental) and one sample of Lower Tertiary porphyritic andesite from Zacatecas are analyzed for ${}^{87}\text{Sr}{}^{86}\text{Sr}$, K, Rb, and Sr. Eight selected samples are also analyzed for ${}^{143}\text{Nd}{}^{144}\text{Nd}$. A linear regression of the present-day ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{and}{}^{87}\text{Rb}{}^{86}\text{Sr}$ of the felsic volcanic rocks in Zacatecas gives an approximate date of 30 ± 8 Ma. The initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios are high and widely distributed (from 0.705 to 0.712 or higher) whereas the initial ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios are somewhat low and show a narrow range (0.5125–0.5127). The available isotopic and trace-element data are best explained in terms of a binary mixing model in which the magmas derived from a slightly depleted-mantle fractionate and mix with varying proportions of the overlying middle/upper continental crust and undergo further shallow-level fractional crystallization before eruption. This model is also compatible with the trace-element and Sr isotopic data published from other areas of the Sierra Madre Occidental for which a purely mantle origin has been proposed.     

Isotopic evidence for genetic relations between acid and alkaline rocks in Italy

Pb isotopic composition and concentrations were determined for whole-rock samples from the Pliocene-Pleistocene, acid, Tuscan Igneous Province, Italy, in order to clarify their relation to the Cenozoic alkaline volcanism of Central Italy. The Pb of the Tuscan rocks is fairly uniform in its isotopic composition, despite variable and high ₈₇Sr/₈₆Sr ratios (0.711–0.725; Barberi et al, 1971).A comparison of the Pb isotopic composition in the Tuscan and the potassic alkaline rocks strongly suggests a continuous mixing relation between both rock series, with partial melts of mantle material and argillaceous sedimentary rocks as likely end-members. Such an interrelation could also provide a simple explanation for the range in the Sr isotopic ratio within the Tuscan rocks. The favoured model envisages a similar history for both rock-series; it is suggested that their main petrographic differences result from a lower portion of mantle-derived material in the parental material for the Tuscan rocks, and from the mineral phases present in the residue during partial melting of the source region.     

Lead isotopic compositions of South Sandwich Island volcanic rocks and their bearing on magmagenesis in intra-oceanic island arcs

Pb isotope ratios have been measured in 12 volcanic rocks from the South Sandwich Islands. The ranges are ${}^{206}\text{Pb}{}^{204}\text{Pb}\text{= 18.51–18.66;}{}^{207}\text{Pb}{}^{204}\text{Pb}\text{= 15.55–15.64;}{}^{208}\text{Pb}{}^{204}\text{Pb}\text{= 38.42–38.64}$. In ${}^{207}\text{Pb}{}^{204}\text{Pb}\text{-}{}^{206}\text{Pb}{}^{204}\text{Pb}$ and ${}^{208}\text{Pb}{}^{204}\text{Pb}\text{-}{}^{206}\text{Pb}{}^{204}\text{Pb}$ correlation diagrams, the South Sandwich data plot distinctly above the fields for ocean ridge basalts, and yield trends showing apparent mixing with a sedimentary end member similar to South Atlantic pelagic sediments as reported by Chow and Patterson (1962) and this study. Armstrong and Cooper (1971) have likewise shown that volcanics from the Lesser Antilles show mixing trends with North Atlantic sediments in Pb isotope correlation diagrams. The North Atlantic sediments have distinctly higher ${}^{206}\text{Pb}{}^{204}\text{Pb}$ and ${}^{208}\text{Pb}{}^{204}\text{Pb}$ ratios compared to the South Atlantic sediments. The parallel relationships between sediments and volcanic island arc rocks of the North and South Atlantic provide strong evidence for a component of Pb from subducted sediments in the lavas of the west Atlantic basin. In contrast to these data, lavas from the Mariana Arc in the western Pacific show little or no component of Pb from pelagic sediments. The reason for the different behaviors in the two settings is speculative.     

Pb isotope geochemistry of a massif-type anorthositic-charnockitic body: The Hidra Massif (Rogaland,S.W. Norway).

The Hidra Massif (Rogaland complex, S.W. Norway) is a massif-type anorthositic-charnockitic body. It consists of undeformed anorthosites and leuconorites, grading into fine-grained jotunites at the contact with the granulite facies gneisses of the metamorphic envelope. A stockwork of charnockitic dykes cross-cuts the massif. The Pb isotopic compositions of the anorthosites and leuconorites are comparable or slightly less radiogenic than those of the jotunites (${}^{206}\text{Pb}{}^{204}\text{Pb}$ from 18.079 to 19.307,(${}^{207}\text{Pb}{}^{204}\text{Pb}$ from 15.568 to 15.657 and ${}^{208}\text{Pb}{}^{204}\text{Pb}$ from 37.617 to 38.493). These values are compatible with an upper mantle origin for the parental magma of jotunitic composition and for the plagioclasic cumulates, but show the incorporation of lower crustal material (U-depleted and thus less radiogenic). The charnockitic dykes have significantly less radiogenic Pb isotopic compositions (${}^{206}\text{Pb}{}^{204}\text{Pb}$ from 17.472 to 19.171, ${}^{207}\text{Pb}{}^{204}\text{Pb}$ from 15.489 to 15.620and ${}^{208}\text{Pb}{}^{204}\text{Pb}$ from 36.991 to 40.922) which can be explained by a larger proportion of lower crustal contamination material. The contaminant could be the granulite facies gneisses of the metamorphic envelope. This interpretation is compatible with the K-Rb relationships of these rocks and with the O and Sr isotopic geochemistry.The proportion of contaminating lead in the charnockitic dykes can be estimated at 55 ± 15% considering the border facies jotunite as the uncontaminated parental magma and the least radiogenic gneiss of the metamorphic envelope as the contaminant.     

Isotopic and geochemical systematics in Tertiary-Recent basalts from southeastern Australia and implications for the evolution of the sub-continental lithosphere

Tertiary-Recent Tasmanian and Newer (Victoria/South Australia) basalts range from quartz tholeiite to olivine melilitite and show systematic increases in their incompatible element abundances with increasing degree of silica undersaturation. These two basalt provinces show similar relative abundances of rare earth elements (REE), differences in the relative concentrations of Rb, Ba, Th, K and Nb, and distinct, restricted isotopic compositions. The Tasmanian basalts have ${}^{87}\text{Sr}{}^{86}\text{Sr}$ from 0.7026 to 0.7034, and ?_Nd from + 7.5 to + 5.8; the Newer basalts have higher ${}^{87}\text{Sr}{}^{86}\text{Sr}$ from 0.7038 to 0.7045, and lower ?_Nd from +4.2 to + 1.7. The range in Sr and Nd isotope compositions can be denned by primary magma compositions for both provinces, using Mg-values, Ni content and the presence of spinel lherzolite nodules. Major and trace element and Sr, Nd and Pb isotope compositions are uniform on a scale of up to 50 km for four separate Newer basanite centers. The chemical and isotopic data are consistent with a model whereby tholeiitic basalts are derived by large degrees of partial melting from a chemically uniform but isotopically variable source, and generation of undersaturated, alkaline basalts by smaller degrees of partial melting of the same source. No isotopic or geochemical evidence was found which would suggest that the more evolved basalts have been contaminated by continental crust.In contrast to tholeiitic and alkalic basalts from Hawaii, there is a continuous spectrum of isotope compositions for the Newer tholeiitic to alkalic basalts. A model is proposed for the generation of these basalts involving mixtures of hotspot mantle plume-derived melt and lithospheric mantle-derived melt, where observed differences between ocean island and continental alkaline basalts are attributed to differences between the sub-oceanic and sub-continental lithospheric mantles. Isotopic differences between tholeiitic and alkalic basalts are interpreted to be due to varying degrees of exchange and mixing between the hotspot plume and lithospheric mantle melt components. The model is consistent with the generation of these basalts from a source which has been recently enriched in the LREE.     

Origin of granitic magma by crustal remobilisation: Rb-Sr and Pb/Pb geochronology and isotope geochemistry of the late Archaean Qôrqut Granite Complex of southern West Greenland

Rb-Sr and Pb/Pb whole rock isochrons on the Qôrqut Granite Complex yield ages of $\text{2530 ± 30}\text{Myr}\text{(}\text{initial}{}^{87}\text{Sr}{}^{86}\text{Sr}\text{= 0.7081 ± 0.0008)}$ and 2580 ± 80 Myr respectively. A model relating initial Sr and Pb isotopic compositions of the Qôrqut granites to the Sr and Pb isotopic compositions of the Amîtsoq gneisses (ca. 3700 Myr) and Nûk gneisses (ca. 2900 Myr) at 2550 Myr ago, as well as Sr and Pb contents of the gneiss units, suggests that between 40 and 50% of the Qôrqut granite magma was generated by partial melting of Amîtsoq gneisses, and the remainder by partial melting of Nûk gneisses.     

Strontium isotope ratios in volcanic rocks from the northwestern part of the Hellenic arc

${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios have been determined in fifteen volcanic rocks from the northwestern part of the Hellenic arc. They range from 0.7041 to 0.7134. There is no apparent correlation of strontium isotope values with any major chemical component or with Rb/Sr ratios. The ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios appear to increase in a general way with increasing depth to the Benioff zone. The strontium isotope ratios are higher than from most island arcs; this is believed to be due to contamination.     

Isotope and trace element geochemistry of sediments from the Barbados Ridge-Demerara Plain region,Atlantic Ocean

Twenty-four piston core sediment samples and 13 sediments and 3 basalts from DSDP Leg 78 Site 543 were analyzed for Sr, Nd and Pb isotopic compositions. The results show sediment with highly radiogenic Pb${}^{206}\text{Pb}{}^{204}\text{Pb}$ up to 19.8) and rather radiogenic Sr and unradiogenic Nd has been deposited in the region since the Cretaceous. The source of this sediment is probably the Archean Guiana Highland, which is drained by the Orinoco River. Pb and Sr isotopic compositions and sediment thickness decrease and${}^{143}\text{Nd}{}^{144}\text{Nd}$ increases northward due to a decrease in turbiditic component. This decrease is partly due to the damming action of basement ridges. Rare earth concentrations in the sediments are somewhat low, due to the abundance of detrital and biogenic components in the sediment and rapid sedimentation rates. Both positive and negative Ce anomalies occur in the surface sediments, but only positive Ce anomalies occur in the Site 543 sediments. It is unlikely that sediment subducted to the source region of Lesser Antilles arc magmas could be the cause of negative Ce anomalies in those magmas.Isotopic compositions of Site 543 basalts show some effect of contamination by seawater-basalt reaction products and sediments. Beyond this, however, they are typical of “normal” depleted MORB.     

Isotopic composition of strontium in Indian kimberlites

Strontium isotopic studies on twenty three whole rock kimberlites from two petrographic provinces in India show variation of initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios from 0.7027 to 0.7102. The variation is unrelated to the degree of alteration. Between the micaceous and basaltic varieties there is some overlap in the Sr isotopic ratios. Leaching experiments on whole rock samples showed more highly radiogenic Sr in leaches compared to the bulk samples.In two diatremes, the initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios show a positive correlation with $\text{Rb}\text{Sr}$ which is believed to reflect a source event earlier than the formation of the kimberlites. The observed Sr isotopic data can be caused by (i) melting of a heterogeneous source or (ii) disequilibrium partial melting in the source region. In the former case, variable isotopic composition would be a necessary consequence of melting in small subsystems.     

Columbia River volcanism: the question of mantle heterogeneity or crustal contamination

Basalts from the Columbia River flood basalt province of the northwestern U.S.A. show a large diversity in chemical and Nd and Sr isotopic compositions. ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ranges from 0.51303 to 0.51208 and is strongly correlated with variations in ${}^{87}\text{Sr}{}^{86}\text{Sr}$. This correlation suggests mixing between two end member compositions, one characterized by ${}^{143}\text{Nd}{}^{144}\text{Nd}\text{> 0.51303}$ and ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{< 0.7035}$, and the other with ${}^{143}\text{Nd}{}^{144}\text{Nd}\text{< 0.5120}$ and ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{> 0.715}$. The more radiogenic component could be mantle enriched in incompatible elements during the Precambrian, or Precambrian materials of the continental crust. A quartz-rich xenolith found in the Columbia lavas has Rb-Sr and Sm Nd model ages of ≈ 1.4Æ, implying the existence of old, isotopically evolved crustal basement which could serve as contaminant. Nevertheless, crustal contamination alone cannot explain the chemical variation of the samples studied, and other fractionation processes must have occurred simultaneously. A model involving combined assimilation and crystal fractionation reproduces the chemical and isotopic characteristics of the volumetrically dominant Grande Ronde unit for an assumed crystallizing component of plagioclase, low calcium pyroxene and minor olivine. The data are not consistent with the suggestion that a ‘primordial’ mantle is the source for this continental flood basalt province. Rather they suggest that the main volume of these lavas was originally derived from a mantle similar in isotopic composition to island arc and ocean island basalts of the north Pacific. The primary magma was modified chemically and isotopically by crystal fractionation and assimilation of sialic crustal materials during its transport through, or storage in the continental crust.