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.     

The Mesoproterozoic Zig-Zag Dal basalts and associated intrusions of eastern North Greenland: mantle plume–lithosphere interaction

The lavas of the Zig-Zag Dal Formation of eastern North Greenland constitute a Mesoproterozoic tholeiitic flood basalt succession up to 1,350 m thick, extending >10,000 km², and underlain by a sill complex. U–Pb dating on baddeleyite from one of the sills thought to be contemporaneous with the lava extrusion, gives an age of 1,382±2 Ma. The lavas, subdivided from oldest to youngest into Basal, Aphyric and Porphyritic units, are dominantly basaltic (>6 wt.% MgO), with more evolved lavas occurring within the Aphyric unit. The most magnesian lavas occur in the Basal unit and the basaltic lavas exhibit a generalised upward decrease in Mg number (MgO/(MgO + Fe₂O₃^T)) through the succession. All of the lavas are regarded as products of variable degrees of olivine, augite and plagioclase fractionation and to be residual after generation of cumulates in the deep crust. The basaltic lavas display an up-section fall in the ratio of light to heavy rare-earth elements (LREE/HREE) but an up-section rise in Zr/Nb, Sc, Y and HREE. The older lavas (Basal and Aphyric units) are characterised by low _Nd and _Hf in contrast to higher values in the younger (Porphyritic unit) lavas. The Porphyritic Unit basalts are characterised by a notable enrichment in Fe and Ti. The Zig-Zag Dal succession is inferred to reflect an increase in melt fraction in the sub-lithospheric mantle, with melting commencing in garnet–lherzolite facies peridotites and subsequently involving spinel-facies mantle at increasingly shallow depths. Melting is deduced to have occurred beneath an attenuating continental lithosphere in conjunction with ascent of a mantle plume. Lithospheric contamination of primitive melts is inferred to have diminished with time with the Porphyritic unit basalts being products of essentially uncontaminated plume-source magmas. The high iron signature may reflect a relatively iron-rich plume source.     

Rare earth element, 87Sr/86Sr,and 143Nd/144Nd compositions of Cenozoic orogenic dacites from Baja California,northwestern Mexico,and adjacent west Texas: evidence for the predominance of a subcrustal component

Dacitic lavas and ignimbrites were examined from seven localities that span the entire 700 km width of the mid- to late Cenozoic magmatic arc of northwestern Mexico and adjacent west Texas. These rocks have remarkably similar REE patterns that are parallel in the heavy REE and have modest negative Eu anomalies. Samples from three localities including Baja California, the Sierra Madre Occidental, and the Chihuahuan Basin and Range have initial ⁸⁷Sr/⁸⁶Sr between 0.7044 and 0.7050 and _Nd near 0.0±1.0. These dacites are isotopically similar to associated basalts, and they show no systematic isotopic variation that is correlated with age or composition of the basement. There is no evidence that magmas parental to these dacites interacted significantly with continental crust. Samples form three other localites in the Basin and Range vary in initial ⁸⁷Sr/⁸⁶Sr from 0.7051 to 0.7070 and _Nd from about -1 to –2. The composition of these rocks reflects contamination of the parental magmas by relatively small amounts of Precambrian crust. Collectively, the dacites of this study show much less isotopic variation than do Mesozoic granitoids (Farmer and DePaolo 1983) and late Cenozoic olivine tholeiites (Hart 1985) from similar transects of the western United States. The distinctive source region for the magmas parental to the Mexican dacites was relatively uniform isotopically, but it was enriched in LIL and HFS elements beneath the eastern Basin and Range.     

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

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

Geochemistry of Picritic and Associated Basalt Flows of the Western Emeishan Flood Basalt Province, China

Picritic lava flows near Lijiang in the late Permian Emeishanflood basalt province are associated with augite-phyric basalt,aphyric basalt, and basaltic pyroclastic units. The dominantphenocryst in the picritic flows is Mg-rich olivine (up to 91·6%forsterite component) with high CaO contents (to 0·42wt %) and glass inclusions, indicating that the olivine crystallizedfrom a melt. Associated chromite has a high Cr-number (73–75).The estimated MgO content of the primitive picritic liquidsis about 22 wt %, and initial melt temperature may have beenas high as 1630–1690°C. The basaltic lavas appearto be related to the picritic ones principally by olivine andclinopyroxene fractionation. Age-corrected Nd–Sr–Pbisotope ratios of the picritic and basaltic lavas are indistinguishableand cover a relatively small range [e.g. _Nd(t) = –1·3to +4·0]. The higher _Nd(t) lavas are isotopically similarto those of several modern oceanic hotspots, and have ocean-island-likepatterns of alteration-resistant incompatible elements. Heavyrare earth element characteristics indicate an important rolefor garnet during melting and that the lavas were formed byfairly small degrees of partial melting. Rough correlationsof isotope ratios with ratios of alteration-resistant highlyincompatible elements (e.g. Nb/La) suggest modest amounts ofcontamination involving continental material or a relativelylow-_Nd component in the source. Overall, our results are consistentwith other evidence suggesting some type of plume-head originfor the Emeishan province. KEY WORDS: Emeishan; flood basalts; picrites; mantle plumes; late Permian     

Petrology,isotope characteristics,and K-Ar ages of the Maranhão,northern Brazil,Mesozoic basalt province

Northern Brazil contains remnants of Mesozoic flood basalts and hypabyssal rocks that were apparently emplaced during tectonism related to opening of the Atlantic Ocean. Analyses and new K-Ar ages reveal that this 700x250 km Maranhão province (5°–8°S) has low-Ti basalts (1.1 wt% TiO₂) in the western part that range about 160 to 190 Ma, and high-Ti basalts (3.4–4.4 wt% TiO₂) in the eastern part about 115–122 Ma. Low-Ti basalt compositions are less evolved and have a smaller range, Mg# 62-56, than the high-Ti basalts, Mg# 44–33. General characteristics of the least evolved members of low- and high-Ti groups include, respectively, Zr 100 and 250 ppm, Sr 225 and 475 ppm, Ba 200 and 500 ppm, Nb 10 and 26 ppm, Y 29 and 36 ppm, La/Yb_(n) 4.2 and 8.8, where La_(n) is 30 and 90. Overall compositions resemble the low- and high-Ti basaltic rocks of the Mesozoic Serra Geral (Paraná) province in southern Brazil. The Maranhão low-Ti basalts have more radiogenic Sr and Pb and higher ¹⁸O than the high-Ti basalts. Respectively, low- vs high-Ti: _Sr26–54 vs 15–18; ²⁰⁶Pb/²⁰⁴Pb=18.25–.78 vs 18.22–.24; and ¹⁸O 8.9–12.6 vs 6.5–8.6. Nd isotopes overlap: _Nd–1.6 to –3.8 vs –2.1 to –3. Ages, compositions, and isotopes indicate that the low- and high-Ti groups had independent parentages from enriched subcontinental mantle. However, both groups can be modeled from one source composition if low-Ti basalt isotopes reflect crustal contamination, and if the parentages for each group were picritic liquids that represent either higher (for low-Ti) or lower (for high-Ti) percentages of melting of that single source. When comparing Pb isotopes of Maranhão and Serra Geral high-Ti basalts (uncontaminated) to evaluate the DUPAL anomaly, Maranhão has Pb 7/4=4.6–11, and Pb 8/4=72–87; Serra Geral has Pb 7/4=10–13, and Pb 8/4=95–125. The small difference is not enough to conform to DUPAL contours, and is inconsistent with large-scale isotopic heterogeneity of mantle beneath Brazil prior to rifting of South America from Africa. Maranhão low-Ti magmas probably relate to the opening of central North Atlantic, and high-Ti magmas to the opening of equatorial Atlantic. The proposed greater percentage of source melting for low-Ti basalts may reflect a Triassic-Jurassic hotspot, while lesser melting for high-Ti magmas may relate to Cretaceous decompressional (rifting) melting.     

Nd and Sr isotopes in the Aleutians: multicomponent parenthood of island-arc magmas

Young volcanic rocks from different sections of the Aleutian Islands-Alaska Peninsula Arc have been measured for ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd and some trace elements. We found the ¹⁴³Nd/¹⁴⁴Nd to be highly restricted in range ( _Nd=6 to 7) and low as compared to midocean ridge ba-salts (MORB). This indicates that the source of the Aleutian Arc magmas is different from MORB and remarkably isotopically homogeneous with respect to Nd. The range reported here for arc rocks is substantially smaller than found by other workers. However, the Sr isotope ratios vary considerably ( _Sr=–24 to –14). Those samples from small volcanic centers north of the main arc (second arc) are characterized by low _Sr. Our data in combination with previous studies suggest that there are slight geochemical differences between discrete sections of the arc. The general uniformity of Nd isotope ratios are thought to be the surface expression of an efficient mixing or homogenization process beneath the arc plate, but which still causes a wide dispersion in Sr isotopic composition.To relate the arc rocks to the broader tectonic setting and to identify possible sources of arc magmas, measurements were done on volcanic and sedimentary rocks from the North Pacific/Bering Sea area. Alkali basalts from the back-arc islands St. George, Nunivak and St. Lawrence and alkali-rich tholeiites from the fore-arc have _Nd=+4 to +9 and are correlated on the _Sr- _Nddiagram parallel to the mantle array but shifted to lower _Sr. These samples are thought to be isotopically representative of the mantle transported to that region. A tholeiitic basalt from the Kamchatka Basin ocean floor (back-arc), however, yielded typical MORB values ( _Nd=10, _Sr=–24). Composite sediment samples were made from DSDP cores in the Aleutian Abyssal Plain, Gulf of Alaska and the Alka Basin which represent mixtures of continentally and arc-derived materials. These composites have intermediate Nd isotopic ( _Nd= –2 and +2) and high Sr isotopic values ( _Sr=+9 and +37). These data show that possible source materials of the Aleutian Arc volcanics are isotopically different from and much more heterogeneous than the arc rocks themselves.On the basis of this study and of literature data, we developed a set of alternative models for volcanic arc magma generation, based on the restricted range in _Nd and the wider range in _Sr for arc rocks. Different isotopic and trace element characteristics found in different arcs or arc sections are explained by varying mixing proportions or concentrations in source materials. The basic observations require rather strict mixing ratios to obtain constant _Nd. The preferred model is one where the melting of subducted oceanic crust is controlled by the amount of trapped sediment with the melting restricted to the upper part of the altered basaltic layer. Homogenization within the upper part of the oceanic crust is brought about by hydrothermal circulation attending dewatering of the slab during subduction and possibly some oxygen exchange of the magmas on ascent.Division Contribution Number 3849 (411)     

The relationship between E- and N-type magmas in the Baffin Bay Lavas

The picritic lavas of Baffin Island represent one of the most primitive Phanerozoic volcanic suites in the world with MgO contents ranging from 22 wt% (29 Mg, cation unit = Mg/100 cations) for olivine-rich lavas to 11 wt% (16 Mg) for olivine-poor lavas. Two magma types can be recognized on the basis of trace element and isotopic geochemistry. N-type magma, which dominates the high-MgO lavas, has depleted LREE patterns [(La/Sm)_N0.6–0.7] typical of N-MORB, K/Ti<0.05, and ⁸⁷Sr/⁸⁶Sr <0.7032. E-type magma, which dominates the lower MgO lavas, has flat to slightly enriched LREE patterns [(La/Sm)_N1.1–1.2] typical of E-MORB, K/Ti>0.5 and ⁸⁷Sr/⁸⁶Sr ranging between 0.7032–0.7039. These two magma types are, however, virtually indistinguishable in terms of major clements and many other trace elements. The E and N-type samples are intermixed throughout the volcanic succession, indicating that both types of magma erupted contemporaneously. Although the compositional spectrum observed for major and highly incompatible elements is consistent with olivine fractionation, crystal fractionation cannot account for the difference in the LREE between E-type and N-type lavas. Crustal contamination involving a lower crust composition cannot reproduce the more magnesian E-type lavas.and can only repoduce the lowest (La/Sm)_N ratios of the E-type lavas if high degrees of assimilation (50%) have occurred. Partial melting models can reasonably account for the distinct (La/Sm)_N ratios and the similar Zr/Y values of the two magma types, but fail to reproduce the observed abundances or REE, Sr, Y and Zr. Compositionally different mantle sources are required to explain the two distinct magma types observed in Baffin Island. A model in which the mantle source is a mixture of enriched plume material and depleted entrained mantle in the head of a mantle plume may explain the contemporaneous eruption of N and E-type magmas in the Baffin Bay picritic suite. The Baffin Island E-type lavas are less enriched in Sr, Y and Zr contents and have lower Zr/Y, for similar (La/Sm)_N than the other E-type lavas of the northern North Atlantic region.     

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 Tertiary tholeiites and picrites from Qeqertarssuaq (Disko Island) and Nuussuaq, West Greenland with implications for the mineral potential of comagmatic intrusions

Tertiary continental flood basalts on Qeqertarssuaq and Nuussuaq in West Greenland contain ～3?km of picrites and variably contaminated tholeiites. The picrites are in the Naujánguit member of the Vaïgat Formation and they have 7–29?wt% MgO, La/Sm?=?0.9–2.1, and ¹⁴³Nd/¹⁴⁴Nd?=?0.51263–0.51307. They appear to have crystallised from high-Mg parental magmas (14.4–16.4?wt% MgO) with isotope and trace element ratios similar to recent Icelandic picrites. Discrete horizons of tholeiites, including the Asûk and?Kûgánguaq, have elevated SiO₂ (50–58 wt%), La/Sm?=?3–7, ⁸⁷Sr/⁸⁶Sr?=?0.70550–0.71224, and low ¹⁴³Nd/¹⁴⁴Nd?=?0.51234–0.51174. These lavas have low Cu and Ni abundances (typically 10–50?ppm Ni or Cu), and in the case of the Asûk on Qeqertarssuaq, they contain droplets of native iron. The low Cu and Ni contents are attributed to scavenging by magmatic sulphides formed in response to crustal contamination of picritic magmas. Two contamination trends are recognised, one to a sediment end-member with high Th/Nb and Archaean model Nd ages, and the other to a meta-igneous component with high La/Sm, low Th/Nb and Rb/Nb, and Proterozoic source ages. Overall, ²⁰⁶Pb/²⁰⁴Pb varies from 16.47–21.68. Both contamination trends are associated with low Cu and Ni, and high SiO₂, and it is argued that the magmatic sulphides were triggered by the increases in silica, rather than simply by the introduction of additional crustal-derived sulphur. Geochemically, the Asûk and Kûgánguaq rocks resemble the most contaminated Nadezhdinsky lavas of the Siberian Trap, which are widely regarded as the source of the Ni and Cu mineralisation in the giant Noril'sk deposits. Mass balance considerations indicate that the parental liquids to the contaminated magmas contained sufficient Ni, Cu, S and platinum group elements to form substantial magmatic sulphide deposits. However, unlike the lavas at Noril'sk, the contaminated (low Cu and Ni) West Greenland basalts are in isolated units with no evidence for a gradual recovery in Ni and Cu abundances with height in the lava column. Comparison with Noril'sk suggests that although significant quantities of metals were scavenged by sulphides in West Greenland, the metal contents of the sulphides may not have been upgraded by continued interaction with subsequent magma batches.     

Sm−Nd and Pb isotopic study of mafic rocks associated with early Proterozoic continental rifting: the Peröpohja schist belt in northern Finland

The Peräpohja schist belt in northern Finland rests unconformably on Archaean granitoids, and marks the early stages of Proterozoic crustal evolution in the Fennoscandian (Baltic) shield. 2440 Ma old layered mafic intrusions predate the supracrustal , and ca. 2200 Ma old sills of the gabbro-wehrlite association intrude the lowest quartzites and volcanics (Runkaus) of the sequence. The Sm-Nd mineral isochron of the Penikat layered intrusion gives an age of 2410±64 Ma. The initial _Nd-values of the Penikat intrusion (_Nd(2440) = –1.6) and the Runkausvaara sill (_Nd(2200) 0) suggest that these mafic magmas were contaminated by older crustal material. The Sm-Nd and Pb isotopic results on the 2.44–2.2 Ga old Runkaus volcanics indicate mobility of Pb, fractionation of Sm/Nd during late greenschist facies metamorphism, and crustal contamination. The Pb-Pb data provide an age of 1972±80 Ma with a high initial ²⁰⁷Pb/²⁰⁴Pb ratio (₁ = 8.49), while scattered Sm-Nd data result in an imprecise age of 2330±180 Ma, with an initial _Nd-value of about zero. Secondary titanite gives an U-Pb age of ca. 2250 Ma. The Jouttiaapa basalts, in contrast, ascended from the mantle without interaction with older crust. These LREE depleted tholeiites mark a break in continental sedimentation, and yield a Sm-Nd age of 2090±70 Ma. Their initial _Nd = + 4.2 ±0.5 implies that the subcontinental early Proterozoic mantle had been depleted in LREE for a long period of time. The first lava flows are strongly depleted in LREE, suggesting that their source was significantly more depleted than the source of mid-ocean ridge basalts today.     

Petrogenesis of anomalous K-enriched MORB from the Southwest Indian Ridge: 11°53′E to 14°38′E

Glassy pillow basalts with unusual geochemical characteristics for mid-ocean ridge basalt (MORB) have been dredge sampled from the Southwest Indian Ridge between 12 and 15°E during Leg ANT IV/4 of the F.S. POLARSTERN. Lavas from 4 of 6 dredges are moderately nepheline normative, highly K-enriched (0.5–1.77 wt% K₂O) alkali basalts and hawaiites. Mg-numbers indicate that many of the lavas are fairly primitive (Mg No.=63–67), yet show extreme enrichment in incompatible elements; e.g. Nb (24–60 ppm), Ba (170–470 ppm) and Sr (258–460 ppm). Incompatible-element ratios such as Zr/Nb (3–5) and Y/Nb (0.46–1.1) are extremely low even for E-type (enriched) MORB, whereas (La/Yb)_n ratios are particularly high (3.4–7.8). ⁸⁷Sr/⁸⁶Sr (0.70290–0.70368), ¹⁴³Nd/¹⁴⁴Nd (0.51302–0.51284) and ²⁰⁶Pb/²⁰⁴Pb (18.708–19.564) isotopic ratios further indicate the geochemically enriched nature of these lavas, which range from the compositional field for depleted N-type (normal) MORB towards the composition of Bouvet Island lavas. Mutually correlated incompatible-element and Sr-, Nd- and Pb-isotopic ratios allow a fairly well constrained model to be developed for the petrogenesis of these unusually alkalic mid-ocean ridge lavas. The alkalic nature and degree of enrichment in incompatible elements is ascribed to particularly low degrees of partial melting (3–5 wt%), at greater than usual depth, of a source region that has experienced prior geochemical enrichment (by veining) related to the upwelling Bouvet mantle plume. To account for the observed compositional variations, a model is proposed whereby mixing between partial melts derived from these geochemically enriched silicate veins, and an incipient to low percentage (±2%) melt from the surrounding geochemically depleted suboceanic asthenosphere occurs as a consequence of increasing degree of melting with adiabatic upwelling. Eruption of these alkalic lavas in this spreading ridge environment is attributed to a temporary hiatus in tholeiitic volcanism and associated spreading along this section of the Southwest Indian Ridge, related to readjustment of spreading direction to a more stable plate geometry.     

Sm-Nd Isotopic and Geochemical Study of the Archean Tonalite-Amphibolite association from the eastern Indian Craton

We report the results of a Sm-Nd isotopic, major element and rare earth element (REE) study of the Older Metamorphic Group (OMG) tonalite-amphibolite association of the eastern Indian Craton. The Older Metamorphic Tonalite Gneisses (OMTG) have been previously dated to be 3.8 Ga using Sm-Nd isotope systematies, and 3.2–3.4 Ga by Rb-Sr and Pb-Pb dating. The results of this study indicate that the protoliths of the OMG amphibolites are 3.3 Ga isochron age=3.30±0.06 Ga, _Nd= +0.9 ± 0.7), and therefore, the OMTG, which intrude into the associated amphibolites, cannot be any older than 3.3 Ga. The amphibolites display light REE enrichment ((Ce/Yb)_N=2.2–6.7; La=30–100 x chondrite) and nearly flat heavy REE patterns ((Tb/Lu)_N=1.2–1.9); the basaltic parents of the amphibolites were probably generated by the partial melting of a spinel lherzolite mantle. Strong linear relationships between the amphibolites and tonalites in ¹⁴⁷Sm/¹⁴⁴Nd-¹⁴³Nd/¹⁴⁴Nd space (isochron age =3.29±0.04 Ga, _Nd= +0.8 ± 0.8) imply that they are genetically related. The tonalites display fractionated REE patterns (La=100–300 x chondrite) with moderate heavy REE depletions ((Tb/Lu)_N=1.9–3.4). The isotopic, major element and REE data are consistent with the derivation of the OMTG from partial melting of OMG amphibolites or equivalent rocks at amphibolegarnet stabilization depths. An initial _Nd(t) value of +0.9±0.7 for the amphibolites indicates the presence of a slightly depleted mantle source at 3.3 Ga with ¹⁴⁷Sm/¹⁴⁴Nd. between 0.20 and 0.22. It is suggested that the growth of continental crust in the eastern Indian craton occurred in response to magmatic underplating in a plume setting.     

Geochemical and mineralogical evidence for the occurrence of at least three distinct magma types in the ‘famous’ region

Bulk rock major and trace element variations in selected basalts from the Famous area, in conjunction with a detailed study of the chemical compositions of phenocryst minerals and associated melt inclusions are used to place constraints on the genetic relationship among the various lava types. The distribution of NiO in olivine and Cr-spinel phenocrysts distinguishes the picritic basalts, plagioclase phyric basalts and plagioclase-pyroxene basalts from the olivine basalts. For a given Mg/Mg+Fe²⁺ atomic ratio of the mineral, the NiO content of these phenocrysts in the former three basalt types is low relative to that in the phenocrysts in the olivine basalts. The Zr/Nb ratio of the lavas similarly distinguishes the olivine basalts from the plagioclase phyric and plagioclase pyroxene basalts and, in addition, distinguishes the picritic basalts from the other basalt types. These differences indicate that the different magma groups could not have been processed through the same magma chamber, and preclude any direct inter-relationship via open or closed system fractional crystallization.The Fe-Mg partitioning between olivine and host rock suggests that the picritic basalts represent olivine (±Cr-spinel) enriched magmas, derived from a less MgO rich parental magma. The partitioning of Fe and Mg between olivine, Cr-spinel and coexisting liquid is used to predict a primary magma composition parental to the picritic basalts. This magma is characterized by relatively high MgO (12.3%) and CaO (12.6%) and low FeO^* (7.96%) and TiO₂ (0.63%).Least squares calculations indicate that the plagioclase phyric basalts are related to the plagioclase-pyroxene basalts by plagioclase and minor clinopyroxene and olivine accumulation. The compositional variations within the olivine basalts can be accounted for by fractionation of plagioclase, clinopyroxene and olivine in an open system, steady state, magma chamber in the average proportions 453223. It is suggested that the most primitive olivine basalts can be derived from a pristine mantle composition by approximately 17% equilibrium partial melting. Although distinguished by its higher Zr/Nb ratio and lower NiO content of phenocryst phases, the magma parental to the picritic basalts can be derived from a similar source composition by approximately 27% equilibrium partial melting. It is suggested that the parental magma to the plagioclase-pyroxene and plagioclase phyric basalts might have been derived from greater depth resulting in the fractionation of the Zr/Nb ratio by equilibration with residual garnet.C.O.B. Contribution No. 722     

Paleoproterozoic (1.90–1.86 Ga) arc volcanism in the Flin Flon Belt,Trans-Hudson Orogen,Canada

Geochemical and isotopic (Nd, Sr) data are reported on Paleoproterozoic (1904–1864 Ma), maficintermediate (<63% SiO₂), arc metavolcanic rocks from the Flin Flon greenstone belt, Manitoba and Saskatchewan. Major element criteria permit subdivision of the rocks into tholeiitic (TH), calc-alkaline (CA), alkaline, and boninitic (BO) magma series. Subaqueously erupted, TH and related CA basalt-basaltic andesite, and rare high-Ca boninites dominated between 1904 Ma and 1890 Ma. The TH rocks are similar to modern island are tholeiites, having low high-field-strength element (HFSE) and rare earth element (REE) abundances, and chondrite-normalized light REE depletion to slight enrichment. The boninites have even lower HFSE and REE abundances (1–2X chondrites). Along with their extreme ratios of refractory incompatible elements (e.g., high Al/Ti, Ti/Zr, low Ti/V, Zr/Y), these features indicate that the arc mantle source was strongly depleted, probably residual after MORB or back-arc basin basalt extraction. Elevated Th/Yb, Ba/La, La/Nb values, and the spread in Nd isotopic compositions (initial _Nd=–0.4 to +4.8) suggest recycling of small amounts (0–8%) of Archean and possibly older Proterozoic crust via sediment subduction and, locally, intracrustal contamination. Calcalkaline andesite-rhyolite and rare shoshonite and trachyandesite, erupted between 1890 Ma and 1864 Ma, are more strongly light REE enriched and have comparatively higher HFSE abundances, and higher Zr/Y and Nb/Y values. The rocks have strong arc trace element signatures (e.g., high Th/Nb, La/Nb), and initial _Nd values (+2.3 to +4.6) indicate that depleted mantle contributions to the magmas continued to be dominant. The geochemistry and geology of these younger volcanic rocks suggest a mature island arc setting in which the arc lithosphere was thicker than in the previous period, and a more fertile sub-arc mantle source was tapped. The pre-1890 Ma volcanism occurred in one or more separate arcs, probably characterized by rapid subduction of oceanic lithosphere, relatively thin, tholeiitic arc crust, and extensive backarc basin formation. In contrast, post-1890 Ma volcanism is dominantly calc-alkaline to (rarely) alkaline, and is interpreted to reflect crustal thickening due to longterm growth of arc edifice(s) and tectonic thickening associated with intraoceanic arc-arc (>1870 Ma) collision and subsequent intra-arc deformation.     

Geochemical and strontium isotopic characteristics of parental Aleutian arc magmas: evidence from the basaltic lavas of Atka

Eighteen flows from a basal stratigraphic sequence on the Aleutian Island of Atka were analyzed for major elements, trace elements and initial ⁸⁷Sr/⁸⁶Sr ratios. Petrographically, these lavas contain abundant plagioclase (24–45%) and lesser amounts of olivine (<7%), magnetite and clinopyroxene phenocrysts. Compositionally, the lavas are high-alumina (20wt%) basalts (48–51 wt% SiO₂) with low TiO₂ (<1%) and MgO (<5%). Within the section, compositional variations for all major elements are quite small. While MgO content correlates with olivine phenocryst contents, no such relationship exists between the other oxides and phenocryst content. These lavas are characterized by 8–10 ppm Rb, high Sr (610–669 ppm), 308–348 ppm Ba and very constant Zr (23–29 ppm) and Sc (23–29 ppm) abundances. Ni and Cr display extremely large compositional ranges, 12–118 ppm and 12–213 ppm, respectively. No correlation exists between trace element concentrations and phenocryst contents. Strontium isotopic ratios show a small but significant range (0.70314–0.70345) and are slightly elevated with respect to typical MORB. No systematic correlation between stratigraphic position and petrography or geochemistry is evident. REE abundances measured on six samples are LREE enriched ((La/ Yb)_N = 2.20–2.81) and display similar chondrite normalized patterns. One sample has a slight positive Eu anomaly but the other lavas do not. Compared to other Aleutian basalts of similar silica content, these lavas are less LREE enriched and have lower overall abundances. The geochemical characteristics of these basalts suggest they represent true liquid compositions despite their highly porphyritic nature. Published phase relations indicate fractionation of a more MgO-rich magma could not have produced these lavas. The high Al₂O₃ and low MgO and compatible element abundances suggest a predominantly oceanic crustal source for parental high-alumina basalts.     

Field setting,mineralogy, chemistry,and genesis of arc picrites,New Georgia,Solomon Islands

The field setting, petrography, mineralogy, and geochemistry of a suite of picrite basalts and related magnesian olivine tholeiites (New Georgia arc picrites) from the New Georgia Volcanics, Kolo caldera in the active ensimatic Solomon Islands arc are presented. These lavas, with an areal extent in the order of 100² km and almost 1 km thick in places, are located close to the intersection of the Woodlark spreading zone with the Pacific plate margin. They contain abundant olivine (Fo_94-75) and diopside (Cr₂O₃ 1.1-0.4%, Al₂O₃ 1–3%), and spinels characterised by a large range in Cr/(Cr+Al) (0.85–0.46) and Mg/(Mg+ Fe⁺⁺) (0.65–0.1). The spinels are Fe⁺⁺⁺ rich, with Fe⁺⁺⁺/ (Fe⁺⁺⁺+Cr+Al) varying from 0.06 to 1.0. A discrete group of spinels with the highest Cr/(Cr+Al) (0.83–0.86) and lowest Fe⁺⁺⁺ contents are included in the most Mg-rich olivine (Fo_91–94) and both may be xenocrystal in origin.The lavas, which range between 10–28% MgO, define linear trends on oxide (element) — MgO diagrams and these trends are interpreted as olivine (0.9) clinopyroxene (0.1) control lines. For the reconstructed parent magma composition of these arc picrites, ratios involving CaO, Al₂O₃, TiO₂, Zr, V and Sc are very close to chondritic. REE patterns are slightly LREE — enriched ((La/Sm)^N 1.3–1.43) and HREE are flat. All lavas show marked enrichments in K, Rb, Sr, Ba, and LREE relative to MORB with similar MgO contents, but the TiO₂ content of the proposed parent magma is close to those of postulated primary MORB liquids. It is proposed that the arc parent magma was produced by partial melting of sub-oceanic upper mantle induced by the introduction of LILE — enriched hydrous fluids derived by dehydration and/or partial melting of subducted ocean crust and possibly minor sediments.     

Nd-Sr isotopic and geochemical systematics in Cambrian boninites and tholeiites from Victoria,Australia

Rocks with boninitic affinities have been recognised in a number of ophiolites, including the Cambrian Heathcote and Mt Wellington Greenstone Belts of Victoria. Boninites and high-Mg andesites from the Heathcote Greenstone Belt show a restricted range of initial _Nd values of between +3.3 to +5.8. Extremely refractory boninites from the Mt Wellington Greenstone Belt have _Nd ranging from +1.3 to –9. Ti/Zr is positively correlated with Sm/Nd with the Heathcote lavas generally possessing greater depletion of Ti and enrichment of Zr relative to the middle and heavy REE with increasing LREE/HREE. These data are consistent with the generation of boninites by partial melting of refractory peridotite following invasion by LREE- and Zr-enriched, low _Nd fluids. Tholeiites overlying the boninites in both greenstone belts have flat REE patterns and _Nd+5, lower than that anticipated for lavas derived from depleted MORB source reservoirs in the Cambrian, suggesting that their source was also contaminated by a LREE-enriched, low _Nd component similar to that involved in the generation of the Howqua boninites. The added components have characteristics compatible with their derivation from subducted altered oceanic crust and/or from wet subducted sediments. The identification of boninites and other low-Ti lavas in the Victorian greenstone belts is strong evidence for island arc development in southeastern Australia during the Lower Cambrian and provides further support for a subduction-related origin for many ophiolites.     

Isotope evidence for ijolite formation by fenitization: Sr−Nd data of ijolites from the type locality Iivaara,Finland

Ijolites from the type locality at Iivaara, Finland, form a continuous series of magmatic rocks ranging from urtites to melteigites. Both Ni and Cr, but also the large ion lithophile light-rare-earth elements, Zr, Hf, Nb, Rb, Sr and Ba are low in concentration. The Nd contents equal those of the neighboring fenites, Sr is distinctly less abundant, and there is no significant Eu anomaly. The ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr of the ijolites demonstrate a systematic covariation between the data of carbonaties from the Kola Alkaline Province (_Sr – 13.8, _Nd + 5.6) and those of the fenites at Iivaara (_Sr + 132.9, _Nd – 24.7) with _Sr varying from +0.3 to +23.9 and _Nd varying from-9.2 to-19.3. The trace element abundances and the isotopic data give evidence for a crystallization of the rocks from a liquid generated by melting (rheomorphism) of high-grade fenitized country rocks rather than from a primary mantle-derived magma which was contaminated at crustal levels. The fenitization of wall rocks preceding the ijolite magma formation was clement selective. Mixing of elements during the fenitization process between the designated components carbonatite (or derivative fenitizing fluid) and wall rock should have been dynamical depending on the stability of the wall rock mineral assemblages in contact with the fenitizing fluids, the migration velocity of these fluids, and their capacity of the respective elements. Such dynamical mixing explains best the variation of the isotope ratios withont systematic covariation of the respective element concentrations.     

Geochemical variations in lavas from Kahoolawe volcano,Hawaii: evidence for open system evolution of plume-derived magmas

The Kahoolawe shield volcano produced precaldera and caldera-filling tholeiites and mildly alkalic post-caldera lavas that petrographically and compositionally resemble such lavas from other Hawaiian shield volcanoes. However, Kahoolawe tholeiites display wide ranges in incompatible trace element ratios (e.g., Nb/Th=9–24, Th/Ta=0.6–1.3), ⁸⁷Sr/⁸⁶Sr (0.70379–0.70440), ¹⁴³Nd/¹⁴⁴Nd (0.51273–0.51298), and ²⁰⁶Pb/²⁰⁴Pb (17.92–18.37). The isotopic variation exceeds that at any other Hawaiian shield volcano, and spans about half the range for all Hawaiian tholeiites. Quasi-cyclic temporal evolution of Kahoolawe tholeiites is consistent with combined fractional crystallization and periodic recharge by primitive magmas. Ratios of highly incompatible trace elements and Sr, Nd, and Pb isotopic ratios from coherent sub-trends that reflect recurrent interactions between variably evolved magmas and two other mantle components whose compositions are constrained by intersections between these trends. The most MgO-rich Kahoolawe tholeiites are partial melts of a high Nb/Th (23.5) ascending plume, possibly comprising ancient subducted oceanic lithosphere. Slightly evolved tholeiites experienced combined crystal fractionation and assimilation (AFC) of material derived from a distinct reservoir (Nb/Th 9) of asthenospheric derivation. The most evolved tholeiites display compositional shifts toward a third component, having mid ocean ridge basalt-like isotopic ratios but enriched OIB-like trace element ratios, representing part of the lithospheric mantle (or melts thereof). Periodic recurrence of all three magma variants suggests that eruptions may have tapped coeval reservoirs distributed over a large depth range. Kahoolawe provides new evidence concerning the nature of the Hawaiian plume, the distribution of compositional heterogeneities in the suboeanic mantle, and the processes by which Hawaiian tholeiites form and evolve.