Oxygen isotope studies of potassic volcanic rocks of the Roman Province,Central Italy

The ¹⁸O/¹⁶O ratios of rocks and coexisting minerals were measured for 93 samples of leucite-bearing lavas, pyroclastics, and related volcanic rocks from the Quaternary Roman Co-Magmatic Province, Italy. The ¹⁸O values were found to generally increase northward in the sequence: Ischia (5.8 to 7.0); Somma-Vesuvius and Phlegrean Fields (7.3 to 8.3); Alban Hills (7.3 to 8.7); M. Sabatini (7.3 to 9.7); Vico Volcano (7.4 to 10.2); and M. Vulsini (8.1 to 11.7). The northward increase in ¹⁸O parallels a similar increase in ⁸⁷Sr/⁸⁶Sr, and these data indicate that the Roman magmas have interacted strongly with high-¹⁸O continental crust. A marked increase in ¹⁸O occurs just north of Rome where the Roman Province begins to overlap the calc-alkaline, oversaturated Tuscan Magmatic Province. Therefore, some of the observed ¹⁸O/¹⁶O and ⁸⁷Sr/⁸⁶Sr enrichments in the Roman magmas may have been facilitated by direct mixing with the high-¹⁸O Tuscan magmas or because the high-¹⁸O country rocks underwent widespread heating during a couple of million years of Tuscan igneous activity. Although many of the Roman magmas underwent fractional crystallization without appreciable change in ¹⁸O, contamination has produced a correlation between ¹⁸O and SiO₂ content at several of the volcanic centers; thus the trachytes are typically higher in ¹⁸O than the undersaturated rocks. The major features of the oxygen isotope data can be explained in terms of a simple two-component mixing model in which one end-member was a primary, strongly undersaturated magma derived from the upper mantle, with ¹⁸O+6, ⁸⁷Sr/⁸⁶Sr0.704 to 0.705, and SiO₂<44wt.%. However, none of the analyzed samples have these values, as they have all been contaminated to some extent. The closest approach is found in some of the leucitepyroxenite ejecta from the Alban Hills. The second end-member, derived from the continental crust, had a variable composition with ¹⁸O+12 to +20, ⁸⁷Sr/⁸⁶Sr0.712 to 0.720, and SiO₂65wt.%, and it mixed in much greater proportions in the volcanoes north of Rome than in those of the Alban Hills or the Naples area. The widespread interactions between the Roman magmas and the continental crust are probably due to (1) the fact that such low-SiO₂ magmas always have a very strong tendency to interact with quartz-bearing rocks of the continental crust, and (2) in Italy, these magmas were emplaced into a tectonically very active area containing poorly consolidated sedimentary rocks, and in the northern part of the belt there had been a prior history of extensive calc-alkaline igneous activity.Publication of the Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, Contribution Number 2501.     

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     

Generation of high-silica rhyolite: A Nd,Sr, and O isotopic study of Sierra La Primavera,Mexican Neovolcanic Belt

High-silica rhyolites of the Sierra La Primavera, a late Pleistocene center near Guadalajara, are extremely Sr-poor (0.3–1.3 ppm), yet (with one exception) values of ⁸⁷Sr/⁸⁶Sr_i are relatively low at 0.7041–0.7048. Values of ¹⁴³Nd/¹⁴⁴Nd for all the rhyolites are (within errors) identical to a basalt at 0.5129. These surprisingly primitive values, along with feldspar ¹⁸O of +6.6, are consistent with an origin by fractional crystallization of mantle-derived basalt. However, absence of the large volume of associated intermediate rocks that would be expected if the 40 km³ of erupted rhyolite were produced mainly by fractional crystallization suggests alternative processes involving partial melting of Mesozoic or Tertiary mafic intrusive rocks (or lower-crustal metamorphic equivalents). The latter interpretation is preferred, especially in light of comparative data for other North American, Cenozoic, high-silica rhyolites. Isotopic compositions correlate with basement age, but generally lie between values for associated basalts and the underlying crust. Nearly all can be interpreted as containing both a young mantle-derived component and a crustal component, probably derived by partial melting at intermediate to deep levels of the crust. No matter what the proportions of mantle- and crust-derived material in parental magmas, the extremely low concentrations of Sr and Ba in the high-silica rhyolites require extensive fractional crystallization of feldspar-rich assemblages after parental liquids attain rhyolitic compositions.At La Primavera, contamination by shallow roof rocks probably led to the 0.708 ⁸⁷Sr/⁸⁶Sr_i ratio of the earliest postcaldera lava dome, which is thought to have erupted through the same vent as the caldera-forming pyroclastic flows. Contamination associated with collapse apparently affected only a small volume of magma in contact with brecciated wall rocks close to the vent, as nearby lavas that erupted during the same episode about 95 ky ago are unaffected. No identifiable lowering of ¹⁸O took place on caldera collapse. Rhyolitic lavas that erupted 75, 60, and 30 ky ago document postcaldera chemical recovery of the chamber to progressively more evolved compositions in its upper reaches, but show little variation in ¹⁸O, ⁸⁷Sr/ ⁸⁶Sr_i, or ¹⁴³Nd/¹⁴⁴Nd with time, suggesting that the bulk of the rhyolitic magma within the chamber was isolated from significant wall-rock contamination. Most of the small range of ⁸⁷Sr/⁸⁶Sr_i among the rhyolites can be attributed to pre-eruptive, in situ decay of ⁸⁷Rb, resulting in a measurable secular increase of ⁸⁷Sr/⁸⁶Sr in these Sr-poor magmas. The ⁸⁷Sr/⁸⁶Sr_i of the youngest rhyolite, however, is somewhat lower than predicted, suggesting that the silicic magma chamber was at times open to interaction with more-mafic magmas from below.     

The geochemistry of potassic lavas from Vulsini,central Italy and implications for mantle enrichment processes beneath the Roman region

Major and trace element and ¹⁴³Nd/¹⁴⁴Nd (0.51209–0.51216) and ⁸⁷Sr/⁸⁶Sr (0.70879–0.71105) isotope analyses are presented on a representative group of lavas from the Vulsini district of the Roman magmatic province. Three distinct series are identified; the high-K and low-K series are similar to those described from other Italian volcanoes, while the third is represented by a group of relative ly undifferentiated leucite basanites which are thought to be near-primary mantle melts. Major and trace element variations within the high-K series are consistent with fractional crystallisation from a parental magma similar to the most magnesian leucitites. Crustal contamination resulted in an increase in ⁸⁷Sr/⁸⁶Sr with increasing fractionation, but it was superimposed on magmas which had already inherited a range of incompatible element and isotope ratios from enrichment processes in the sub-continental mantle. These are reviewed using the available results from Vulsini, Roccamonfina and Ernici. Transition element abundances and Ta/Yb ratios indicate that the pre-enrichment mantle was similar to that of E-type MORB, and that these elements were not mobilised by the enrichment process. Mixing calculations suggest that three components were involved in the enrichment process; mantle comparable with the source of MORB, and two other components rich in trace elements. One, the low-K component, had high Sr/Nd, Th/Ta and Ba/Nb and no europium anomaly while the second had lower Sr/Nd, a negative europium anomaly and very high Th/Ta. It was also characterised by low Nb/Ba and high Rb/Ba ratios, similar to those reported from phlogopite-rich peridotite xenoliths. The trace element enrichment processes are therefore thought to have occurred in the mantle wedge above a subduction zone with the trace element characteristics of the high-K end-member reflecting the subduction of sediments and the stabilisation of mantle phlogopite.     

Implications of Quaternary volcanism at Cerro Tuzgle for crustal and mantle evolution of the Puna Plateau,Central Andes,Argentina

The high-K Tuzgle volcanic center, (24° S, 66.5° W) along with several small shoshonitic centers, developed along extensional Quaternary faults of the El Toro lineament on the east-central Puna plateau, 275 km east of the main front of the Andean Central Volcanic Zone (CVZ). These magmas formed by complex mixing processes in the mantle and thickened crust (>50 km) above a 200 km deep scismic zone. Tuzgle magmas are differentiated from shoshonitic series magmas by their more intraplate-like Ti group element characteristics, lower incompatible element concentrations, and lower ⁸⁷Sr/⁸⁶Sr ratios at a given Nd. Underlying Mio-Pliocene volcanic rocks erupted in a compressional stress regime and have back-arc like calc-alkaline chemical characteristics. The Tuzgle rocks can be divided into two sequences with different mantle precursors: a) an older, more voluminous rhyodacitic (ignimbrite) to mafic andestitic (56% to 71% SiO₂) sequence with La/Yb ratios <30, and b) a younger andesitic sequence with La/Yb ratios >35. La/Yb ratios are controlled by the mafic components: low ratios result from larger mantle melt percentages than high ratios. Shoshonitic series lavas (52% to 62% SiO₂) contain small percentage melts of more isotopically enriched arc-like mantle sources. Some young Tuzgle lavas have a shoshonitic-like component. Variable thermal conditions and complex stress system are required to produce the Tuzgle and shoshonitic series magmas in the same vicinity. These conditions are consistent with the underlying mantle being in transition from the thick mantle lithosphere which produced rare shoshonitic flows in the Altiplano to the thinner mantle lithosphere that produced back-are calc-alkaline and intraplate-type flows in the southern Puna. Substantial upper crustal type contamination in Tuzgle lavas is indicated by decreasing Nd (-2.5 to-6.7) with increasing ⁸⁷Sr/⁸⁶Sr (0.7063 to 0.7099) ratios and SiO₂ concentrations, and by negative Eu anomalies (Eu/Eu^* <0.78) in lavas that lack plagioclase phenocrysts. Trace element arguments indicate that the bulk contaminant was more silicic than the Tuzgle ignimbrite and left a residue with a high pressure mineralogy. Crustal shortening processes transported upper crustal contaminants to depths where melting occurred. These contaminants mixed with mafic magmas that were fractionating mafic phases at high pressure. Silicic melts formed at depth by these processes accumulated at a mid to upper crustal discontinuity (decollement). The Tuzgle ignimbrite erupted from this level when melting rates were highest. Subsequent lavas are mixtures of contaminated mafic magmas and ponded silicic melts. Feldspar and quartz phenocrysts in the lavas are phenocrysts from the ponded silicic magmas.     

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.     

Geochemistry and petrogenesis of the early Tertiary lava pile of the Isle of Mull,Scotland

Major and trace element analyses and strontium isotope ratios are presented for twenty-four samples of lavas and plugs from the early Tertiary lava pile in Mull. The samples were selected on the basis of petrographic freshness from a large collection from outside the hydrothermally altered zone of pneumatolysis which occupies the central region of the volcanic complex. Most of the analyses yield normative hypersthene and we argue that these are essentially unaltered magmatic compositions. The analytical data indicate that the samples may be divided into three groups on the basis of major element chemistry, initial ⁸⁷Sr/⁸⁶Sr ratios and correlations between lithophile element contents. Group I comprises an alkaline series (basalt-hawaiite-mugearite) with extremely low initial ⁸⁷Sr/⁸⁶Sr ratios (0.7030) and generally low lithophile element contents. Apart from their alkalinity and high Sr and Zr contents these samples have affinities with abyssal tholeiites. Group II contains hypersthene normative basalts with more tholeiitic characteristics but (as in the case of the Skye Main Lava Series) the more evolved rocks are trachytes. This group is characterized by more normal levels of lithophile element concentrations and relatively high initial ⁸⁷Sr/⁸⁶Sr ratios of about 0.7055. Group III is less clearly defined and contains basalts that are generally sparsely olivine-phyric and in most chemical respects fall between Group I and Group II-including initial ⁸⁷Sr/⁸⁶Sr ratios (0.7033 to 0.7043). They may represent mixtures of Group I and Group II type sources or magmas. Groups I and II appear to be similar, respectively, to the relatively sodic iron-rich and the relatively potassic ironpoor silica enrichment trends distinguished in the Skye Main Lava Series. In the Group I magma series the behaviour of Y and Sr relative to other incompatible elements can only be explained by differential partial melting of a deep garnet-lherzolite mantle source. Fractional crystallization has undoubtedly occurred at some stage during the ascent of these magmas from the mantle, as indicated by the behaviour of Ni and Cr, but has not been a major factor in the production of evolved magma compositions. The Group II magmas appear to have originated from a source more enriched in lithophile elements, and a relatively shallow (< 50 km) plagioclase-lherzolite mantle source is suggested for these magmas because they have Sr/Ba ratios between one and two orders of magnitude lower than those characteristic of Group I. Rb-Sr systematics suggest that the vertical heterogeneity of the mantle which was largely responsible for the chemical differences between these three groups may have existed for a very long time prior to Tertiary magmatism.     

Carbon and oxygen isotopic composition of carbonates in lavas and ejectites from the Alban Hills,Italy

Carbon and oxygen isotopic analyses have been carried out on carbonates from lavas, ejectites and sedimentary formations in the region of the Alban Hills.The calcite occurring in the lavas, both in veins and cavities and dispersed in the groundmass shows within each flow a fairly uniform isotopic composition not different from that normally observed in sedimentary carbonates, except in the case of one particular flow, where unusually low ¹³C values were recorded. The latter are discussed in terms of a possible contribution of organic carbon or of isotopically light carbonates, the presence of which in the Alban Hills area had been previously recorded.The ejectites examined comprise both limestone and dolostone blocks of various degree of metamorphism and materials of uncertain origin, some of which containing carbon and oxygen of isotopic composition wholly different from that of all carbonates analysed in this work, approaching the range observed in some carbonatites. The isotopic data and the geochemical features of the latter materials are discussed in terms of thermal metamorphism of limestones and of a possible syntexis of evaporite materials.The ¹⁸O and ¹³C values of certain marine limestones from major Mesozoic sedimentary formations in the region are also reported.     

Strontium isotopic and selected trace element variations between two Aleutian volcanic centers (Adak and Atka): implications for the development of arc volcanic plumbing systems

Major and trace element concentrations and initial ⁸⁷Sr/⁸⁶Sr ratios of lavas from the Aleutian volcanic centers of Adak and Atka have been used to study the evolution of their respective lithospheric plumbing systems. The centers are within 150 km of one another and show similar overall silica ranges (47–67%), but Adak (40 km³) is smaller than Atka (200 km³). Adak's lavas are chemically and isotopically heterogeneous (⁸⁷Sr/⁸⁶Sr:0.70285–0.70330) and two units contain lithospheric xenoliths. The lavas of the much larger Atka, on the other hand, have much less variability in major and trace elements as well as ⁸⁷Sr/⁸⁶Sr (0.70320–0.70345). We suggest that these characteristics are a measure of the relative maturity and cleanliness of the lithospheric plumbing systems that supply magma to these centers. Because Aleutian volcanic centers often remain fixed for relatively long periods of time (5 m.y.), once established, magmatic passageways are repeatedly used. Young plumbing systems are relatively cool and contain large amounts of wallrock contaminant, and ascending magmas undergo contamination as well as concurrent crystallization and fractionation. With time, however, heat and mass transfer between ascending magmas and wallrock produce thermal and chemical boundary layers that insulate subsequent magmas. In effect, the plumbing system matures. The chemical heterogeneity displayed by young, dirty systems (like Adak) reflects not only the magma source but also the wallrock encountered during ascent and possibly the effects of extensive crystal fractionation. Thus, it is the petrologic data of mature, clean systems, like Atka, that yield the most direct and unambiguous information on the ultimate origin of the lavas and their near surface evolution.     

Nd- and Sr-isotopic compositions of lavas from the northern Mariana and southern Volcano arcs: implications for the origin of island arc melts

Nd- and Sr-isotopic data are reported for lavas from 23 submarine and 3 subaerial volcanoes in the northern Mariana and southern Volcano arcs. Values of _Nd range from +2.4 to +9.5 whereas ⁸⁷Sr/⁸⁶Sr ranges from 0.70319 to 0.70392; these vary systematically between and sometimes within arc segments. The Nd-and Sr-isotopic compositions fall in the field of ocean island basalt (OIB) and extend along the mantle array. Lavas from the Volcano arc, Mariana Central Island Province and the southern part of the Northern Seamount Province have _Nd to +10 and ⁸⁷Sr/⁸⁶Sr=0.7032 to 0.7039. These are often slightly displaced toward higher ⁸⁷Sr/⁸⁶Sr at similar _Nd. In contrast, those lavas from the northern part of the Mariana Northern Seamount Province as far north as Iwo Jima show OIB isotopic characteristics, with _Nd and ⁸⁷Sr/⁸⁶Sr=0.7035 to 0.7039. Plots of ⁸⁷Sr/⁸⁶Sr and _Nd versus Ba/La and (La/Yb)_n support a model in which melts from the Mariana and Volcano arcs are derived by mixing of OIB-type mantle (or melts therefrom) and a metasomatized MORB-type mantle (or melts therefrom). An alternate interpretation is that anomalous trends on the plots of Nd- and Sr-isotopic composition versus incompatible-element ratios, found in some S-NSP lavas, suggest that the addition of a sedimentary component may be locally superimposed on the two-component mixing of mantle end-members.     

Paricutin re-examined: a classic example of crustal assimilation in calc-alkaline magma

Following its birth on the 20th of February 1943, the Mexican volcano Paricutin discharged a total of 1.38 km³ of basaltic andesite and andesite before the eruption came to an end in 1952. Until 1947, when 75% of the volume had been erupted, the lavas varied little in chemical or isotopic composition. All were basaltic andesites with 55 to 56% SiO₂, ¹⁸O of +6.9 to 7.0, and ⁸⁷Sr/⁸⁶Sr ratios close to 0.7038. Subsequent lavas were hypersthene andesites with silica contents reaching 60%, ¹⁸O values up to +7.6, and ⁸⁷Sr/⁸⁶Sr of 0.7040 to 0.7043. The later lavas were enriched in Ba, Rb, Li, and K₂O and depleted in MgO, Cu, Zn, Cr, Ni, Sr, and Co. The isotopic and other chemical changes, which appeared abruptly over a few months in 1947, are interpreted as the result of tapping a sharply zoned and density stratified magma chamber. Xenoliths of partially fused felsic basement rocks in the lavas have silica contents greater than 70%, ¹⁸O of +5.6 to 9.9 and ⁸⁷Sr/⁸⁶Sr between 0.7043 and 0.7101. In many respects they resemble samples of basement rocks collected from nearby outcrops. Three analysed samples of the latter have silica contents of 65 to 67%, ¹⁸O of +7.7 to 8.6, and ⁸⁷Sr/⁸⁶Sr between 0.7047 and 0.7056.These new data provide strong support for the original interpretations of Wilcox (1954), who explained the chemical variations by a combination of fractional crystallization and concurrent assimilation of up to 20 weight % continental crust. Except for a few trace elements, particularly Ba, Sr, and Zr, the chemical and isotopic compositions of the xenoliths and basement rocks that crop out nearby match the type of contaminant required to explain the late-stage lavas. Some of the discrepancies may be explained by postulating a contaminant that was older and richer in Ba, Sr, and Zr than those represented by the analysed xenoliths. Others can be attributed to chemical changes accompanying disequilibrium partial melting, contact metamorphism, and meteoric-hydrothermal alteration of the country rock. Many of the xenoliths show evidence of having been affected by such processes.The lavas were erupted from a zoned magma chamber that had differentiated by liquid fractionation prior to the eruption. The order of appearance of the lavas can be explained in terms of withdrawal of stratified liquids of differing densities and viscosities.     

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.     

Initial 87Sr/86Sr ratios of plutonic rocks from Japan

Initial ⁸⁷Sr/⁸⁶Sr rations were determined for more than 80 plutonic rocks in Japan. The ⁸⁷Sr/⁸⁶Sr ratios of gabbroic and granitic rocks show no significant difference in plutonic terranes where both rocks occur closely associated, implying a genetic relationship between them (e.g., Green Tuff belt) or reequilibration at deep level (e.g., Ryoke belt). Wherever granitic rocks occur independently from gabbroic rocks, the granites have higher ratios than the gabbros.Initial ⁸⁷Sr/⁸⁶Sr ratios of the granitic rocks are low (<0.706) in Northeast Japan but high (<0.706) in Southwest Japan, the boundary being the Tanakura Tectonic Line. Within Southwest Japan, the ratios are low along the Japan Sea side of the southernmost area. This regional variation is generally correlated with thickness of the continental crust as deduced from the Bouguer anomaly.Initial ⁸⁷Sr/⁸⁶Sr ratios of the granitic rocks vary from 0.7037 to 0.7124. The low group (<0.706) is considered to consist of essentially mantle-derived magmas contaminated by crustal material in lesser but varying degree, because of its geological setting and initial ⁸⁷Sr/⁸⁶Sr values. The high group may have been formed by contamination of a deep-seated magmas by crustal material or by generation of the main part of the magmas within the continental crust. The ratios of individual belts reflect their own history depending upon age and Rb/Sr ratio of the crustal material.Initial ⁸⁷Sr/⁸⁶Sr ratios of granitic rocks are generally low for the magnetite-series but high for the ilmenite-series. Thus, a negative correlation is observed between initial ratios and ³⁴S for most Cretaceous-Paleogene granites. However, Neogene ilmenite-series granites are low in both initial ⁸⁷Sr/⁸⁶Sr and ³⁴S indicating interaction of the granitic magma with young sedimentary rocks enriched in ³²S.     

The Arc Lavas of the Shirahama Group, Japan: Sr and Nd Isotopic Data Indicate Mantle-Derived Bimodal Magmatism

New Sr and Nd isotopic data are presented and integrated withprevious data for the Shirahama Group Mio-Pliocene medium-Kvolcanic are suite of south-central Honshu, Japan. Main resultsare: (1) The Shirahama lavas range in ⁸⁷Sr/⁸⁶Sr from 0.70315to 0.70337 and in ¹⁴³Nd/¹⁴⁴Nd from 0.51298 to 0.51306; the Srand Nd isotopic data cluster tightly within the mantle array,and all lie within an overlapping field of mid-ocean ridge basaltand ocean island basalt; (2) small differences exist among theShirahama tholeiitic series, calc-alkaline series and mixedlavas. The present isotopic data are consistent with a previouslypublished model, which proposes that chemical variations inmagmas of coexisting tholeiitic and calc-alkaline series areproduced through crystal fractionation from mantle-derived magmasof basalt and magnesian andesite, respectively. Moreover, thetholeiitic series and the calc-alkaline series are isotopicallyidentical. Thus, both magma series can be derived from a sourcemantle with the same isotopic composition, supporting the hypothesisof simultaneous generation of basalt and magnesian andesitemagmas from a single diapir rising through the mantle wedgeabove the subduction zone. The differences of water contentand temperature within the diapir are again thought to havebeen produced through dehydration and heating of an isotopicallyhomogeneous hydrous diapir. The isotopic data show that thehigh-SiO₂ lavas have the same isotopic compositions as moremafic lavas. These data and liquid lines of descent of the Shirahamamagmas suggest that even rhyolites can be produced by differentiationfrom mantle-derived magmas without crustal contamination. Analysesfrom 38 other arc volcanoes have been compiled to investigatethe intravolcano variability of ⁸⁷Sr/⁸⁶Sr. Twelve of these displayno intravolcano strontium isotopic variability, as is the casewith the Shirahama Group, but others show greater variationof ⁸⁷Sr/⁸⁶Sr from individual volcanic centers, presumably reflectingcrustal contamination. Most of the latter volcanoes are underlainby thick continental crust. It is noteworthy, however, thatthe greater variations of ⁸⁷Sr/⁸⁶Sr correlate with SiO₂ content;andesites or dacites, not basalts, from the same volcano havethe lowest ⁸⁷Sr/⁸⁶Sr, and these rocks are calc-alkaline in termsof FeO^*/MgO and SiO₂ Theoretically, assimilation of continentalcrust by the isotopically uniform Shirahama magmas could producethese relationships. Given that mantle-derived basalt and magnesianandesite both encounter continental crust on their ascent tothe surface, the hotter basalt magma would assimilate more crustalwallrocks than the cooler andesite, resulting in the basaltbeing more radiogenic. Fractional crystallization, magma mixing,and/or assimilation-fractional crystallization of these magmasin crustal magma chambers could produce large compositionalvariations, but the derivatives of the hotter basaltic magmas(tholeiitic series in the broad sense) would display greatercontamination than those derived from the cooler andesitic magmas(calc-alkaline series). ^*Telephone: 81-858-43-1215. Fax: 81-858-43-2184. e-mail: tamura{at}misasa.okayam-u.ac.jp     

Spatial variations in the geochemistry of quaternary lavas across the Sunda arc in Java and Bali

Since Mesozoic time, Java and Bali have formed part of an evolving system of island arcs comprising the Sunda arc of Indonesia. The present tectonic setting is relatively simple with subduction occurring at the Java Trench to the south. A north-dipping Benioff seismic zone delineates an underthrust lithospheric slab to depths of approximately 600 km beneath the Java Sea. Quaternary lavas of the normal island arc association range from tholeiites to high-K calc-alkaline lavas over Benioff zone depths from 120–250 km, respectively. More abundant calc-alkaline lavas lie between these extremes. High-K alkaline lavas are found over Benioff zone depths in excess of 300 km.Both within and between these groups of rocks there are consistent spatial variations in the observed geochemistry. For approximately 200 rocks, incompatible elements such as K, Rb, Cs, Sr, Ba, light REE, U and Th show an increase in abundance of almost an order of magnitude with increasing depth to the seismic zone. Abundances of compatible elements show little consistent variation and trace elements such as Ni, Co, Cr, and Sc are characteristically depleted except in some of the alkaline lavas. Major element abundances in rocks of the normal island arc association show little variation, except for K and P, which both increase in abundance across the arc and Al, which shows a relative decrease.The major and trace element data are inconsistent with the derivation of the analyzed rocks by partial melting of the crustal component of the subducted lithosphere. On the other hand, low Ni abundances (20 ppm) in the basalts suggest that most of the lavas are fractionated and few if any represent primary mantle-derived melts. The spatial variations in the geochemistry of erupted lavas across Java and Bali are best explained by a combination of two processes: melting of a geochemically zoned mantle source and smaller degrees of partial melting of that material at progressively greater depths. Primary tholeiitic magmas could be formed by 20–25% melting at depths of 30–40 km, primary high-K calc-alkaline magmas by 5–15% melting at 40–60 km depth, and primary alkaline magmas by 5% melting at depths of 80–90 km. The geochemical zoning in the mantle, which is also manifested by increasing ⁸⁷Sr/⁸⁶Sr ratios in lavas across the arc, is interpreted to result from the addition of a small melt fraction derived from the crustal component of the subducted lithosphere.     

Geochemistry of a transitional ne-trachybasalt — Q-trachyte lava series from Patmos (Dodecanesos), Greece: further evidence for fractionation,mixing and assimilation

Trace-element and preliminary Sr- and O-isotopic data are reported for a transitional alkaline-sub-alkaline lava series (MVS) from Patmos, Greece. The lava types belonging to this series are ne-trachybasalt, hy-trachybasalt, hy-trachyandesite and Q-trachyte. Rb, Sr and Ba contents, as well as K/Rb ratios, of the ne-trachybasalts differ from those of alkali basalts of oceanic islands and those of K-rich alkaline lavas of continental regions and are consistent with the occurrence of these volcanics in a destructive plate margin environment. Qualitatively, the variations shown by many trace elements throughout the MVS are explicable in terms of magma evolution via fractional crystallization involving removal of the observed phenocryst phases. Cross-cutting REE patterns can be explained by removal of small amounts of apatite. However, certain features of the data cannot be reconciled with the operation of fractional crystallization alone. These are: a) the compatible behavior of Ba throughout the MVS; b) the moderately (as opposed to highly) incompatible behavior of Zr, Rb and Nb relative to Th; and c) the significant decrease of K/Th, Rb/Th, Zr/Th, Zr/Nb, Nb/Th, Yb/Th, Ta/Th, U/Th and Zr/Ta ratios especially (but not exclusively) in the mafic part of the series. Quantitative modeling indicates that the hy-trachybasalts are anomalously enriched in both highly incompatible and highly compatible elements and these lavas are shown to be hybrids formed by mixing of ne-trachybasalt and hy-trachyandesite. Mixing proportions of the end members calculated from incompatible element abundances (19% ne-trachybasalt) differ from those calculated from compatible element abundances (62% ne-trachybasalt) and are inconsistent with proportions calculated from published mineral chemical data. In addition, mixing cannot account for the observed variations in incompatible element ratios and this is taken as evidence for the simultaneous operation of assimilation. Isotopic variations (⁸⁷Sr/ ⁸⁶Sr from 0.7049 to 0.7076 and ¹⁸O/¹⁶O from 4.7 to 8.6) and the positive correlation of isotope ratios with SiO₂ and Th contents provide conclusive proof that assimilation occurred. Calculations show that the isotopic characteristics and the concentrations of many trace elements in the Q-trachytes can be explained by fractional crystallization of ne-trachybasalt combined with assimilation of average continental crust (⁸⁷Sr/⁸⁶Sr-0.710), and that large amounts of assimilation are not necessary (Ma/Mc=0.55). REE data are not well explained by this model and suggest a crustal end-member enriched in LREE relative to the average crust. Zr and Hf data are also not well explained and indicate that the assimilant was depleted in HFSE relative to average crust or that HFSE are held back in relatively insoluble phases such as zircon in the restite during assimilation. Nevertheless, the results of the modeling demonstrate that Ba concentrations may decrease during AFC processes and that high Sr contents (1500 ppm in the MVS ne-trachybasalts) do not render mafic, parental magmas immune to the effects of assimilation in terms of their ⁸⁷Sr/⁸⁶Sr ratios. The results of this study confirm conclusions based upon major-oxide and mineral chemical data for the MVS lavas but, more importantly, show that careful analysis of trace element data allows the various processes involved in magma evolution to be identified and quantified, even in the absence of major oxide and isotopic data. Finally, it is reiterated that magma mixing and assimilation may be coupled processes in the magma chambers beneath many volcanic centers, and recognition of this fact has profound implications for studies of magmas erupted at continental margins and through continental crust.     

Evidence from Muriah, Indonesia, for the Interplay of Supra-Subduction Zone and Intraplate Processes in the Genesis of Potassic Alkaline Magmas

The high-K alkaline volcano Muriah is situated in central Javaand has erupted two lava series, a younger highly potassic series(HK) and an older potassic series (K). The HK series has higherK2O contents for a given MgO content; greater silica undersaturation;and higher concentrations of LILE (Rb, Sr, Ba, and K), LREE(La and Ce), and HFSE (Nb, Zr, Ti, and P), than the K series.The HK series lavas have incompatible trace element patternssimilar in many respects to ocean island basalts. The K serieshas slightly higher ⁸⁷Sr/⁸⁶Sr (O70453 [GenBank] -O70498) and ¹⁸O (+6?2to + 8?4%o) and lower ¹⁴³Nd/¹⁴⁴Nd (0?512530–0?5126588)than the HK series (for which 87Sr/86Sr = 0?70426–0?70451,<518O = +6?52 to +7–0%o, and 1*3Nd/1*4Nd= 0?512623–0?512679),and higher LILE/HFSE and LREE/ HFSE ratios. A7/4 and A8/4 arehigh and do not show any systematic change from the K to theHK series. The proposed model for the Muriah lavas involvesthree source components: (1) the astheno-sphere of the mantlewedge of the Sunda arc, which has Indian Ocean MORB characteristics;(2) a metasomatic layer situated at the base of the lithosphere,which has characteristics similar to enriched mantle (i.e.,EMU); (3) subducted pelagic sediments from the Indian Ocean. Trace element and isotope data indicate that the characteristicsof the K series are produced by mixing of two endmember magmas:an undersaturated magma derived wholly from within-plate sourcesand a calc-alkaline magma derived from the subduction-modifiedasthenospheric mantle. The calc-alkaline magma is believed tobe contaminated by the arc crust before mixing. Low-pressurefractionation took place in the K series after mixing. Initiallithospheric extension in the Bawean trough (in which Muriahis located), may be responsible for decompressive melting ofthe metasomatic layer and thus the production of the HK serieslavas. The magmas erupted from Muriah show a transition fromintraplate to subduction zone processes in their genesis.     

The petrogenesis of 30–20 Ma basic and intermediate volcanics from the Mogollon-Datil Volcanic Field,New Mexico,USA

In the western USA calcalkaline magmas were generated hundreds of kilometres from the nearest destructive plate margin, and in some areas during regional extension several Ma after the cessation of subduction. The Mogollon-Datil Volcanic Field (MDVF) in southern New Mexico was a centre of active magmatism in the mid- to late-Tertiary, and a detailed field, petrographic and geochemical study has been undertaken to evaluate the relations between extensional tectonics and calcalkaline magmatism in the period 30–20 Ma. The rocks comprise alkalic to high-K calcalkaline lavas, ranging from basalt to high silica andesitc. Most of the basaltic rocks have relatively low HFSE abundances, elevated ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd, similar to many Tertiary basalts across the western USA, and they are inferred to have been derived from the continental mantle lithosphere. Two differentiation trends are recognised, with the older magmas having evolved to more calcalkaline compositions by magma mixing between alkalic basaltic andesites and silicic crustal melts, and the younger rocks having undergone 30–40% fractional crystallisation to more alkalic derivatives. The younger basalts also exhibit a shift to relatively higher HSFE abundances, with lower ⁸⁷Sr/⁸⁶Sr and higher ¹⁴³Nd/¹⁴⁴Nd, and these have been modelled as mixtures between an average post-5 Ma Basin and Range basalt and the older MDVF lithosphere-derived basalts. It is argued that the presence of subduction-related geochemical signatures and the development of calcalkaline andesites in the 30–20 Ma lavas from the MDVF are not related to the magmatic effects of Tertiary subduction. Rather, basic magmas were generated by partial melting of the lithospheric mantle which had been modified during a previous subduction event. Since these basalts were generated at the time of maximum extension in the upper crust it is inferred that magma generation was in response to lithospheric extension. The association of the 30–20 Ma calcalkaline andesites with the apparently anorogenic tectonism of late mid-Tertiary extension, is the result of crustal contamination, in that fractionated, mildly alkaline, basaltic andesite magmas were mixed with silicic crustal melts, generating hybrid andesite lavas with calcalkaline affinities.     

High-18O igneous rocks from the Tuscan Magmatic Province,Italy

The ¹⁸O/¹⁶O ratios were measured for 60 rocks and coexisting minerals from the Plio-Pleistocene, calc-alkaline, Tuscan Magmatic Province, Italy. The ¹⁸O values of these magmas were as follows: Elba, Giglio, and Montecristo granodiorites (11.4 to 12.1); M. Cimini rhyolites and trachytes (11.2 to 11.7); Roccastrada, S. Vincenzo, and M. Amiata rhyolites (12.3 to 13.4); and the Tolfa rhyolites and quartz latites (15.3 to 16.4). The latter are by far the highest ¹⁸O values yet reported for primary volcanic rocks. The extremely high ¹⁸O values in the Tuscan Province indicate that these magmas all formed by melting or large-scale assimilation of high-¹⁸O argillaceous sedimentary rocks, in agreement with previous evidence based on the high ⁸⁷Sr/⁸⁶Sr ratios and ubiquitous presence of cordierite. Low ¹⁸O values (+5 to +6) were found in the feldspar, but not the quartz, of the small Porto Azzuro stock on Elba, as well as in the marginal facies of the M. Capanne stock, indicating that these bodies interacted with low-¹⁸O meteoric-hydrothermal fluids subsequent to solidification. The M. Cimini lavas apparently formed about 1 m.y. ago by mixing of high-¹⁸O Tuscan magmas containing large K feldspar crystals with potassic, undersaturated, low-¹⁸O magmas of the adjacent Roman Co-Magmatic Province. These large sanidine crystals did not completely equilibrate ¹⁸O/¹⁶O with the coexisting magma.Publication of the Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, Contribution Number 2639.     

Multiple Isotopic Components in Quaternary Volcanic Rocks of the Cascade Arc near Crater Lake, Oregon

Quaternary lavas and pyroclastic rocks of Mount Mazama, CraterLake caldera, and the surrounding area have variable Sr, Nd,and Pb isotopic compositions. High-alumina olivine tholeiites(HAOT) have ⁸⁷Sr/⁸⁶Sr ratios of 0.70346–0.70364; basalticandesite, 0–70349–0.70372; shoshonitic basalticandesite, 0.70374–0.70388; and andesite, 0.70324–0.70383.Dacites of Mount Mazama have ⁸⁷Sr/⁸⁶Sr ratios of 0.70348–0.70373.Most rhyodacites converge on 0.7037. However, rhyodacite ofthe caldera-forming, climactic eruption has ⁸⁷Sr/⁸⁶Sr=0.70354because of an admixed low-⁸⁷Sr/⁸⁶Sr component. Andesitic tomafic-cumulate scoriae of the climactic eruption, and enclavesin preclimactic rhyodacites, cluster in two groups but shownearly the entire ⁸⁷Sr/⁸⁶Sr range of the data set, confirmingpreviously suggested introduction of diverse parental magmasinto the growing climactic chamber. Pb and Nd isotope ratiosdisplay less variation (²⁰⁶Pb/²⁰⁴Pb= 18.838–18.967, ²⁰⁷Pb/²⁰⁴Pb=15.556–15.616,²⁰⁸Pb/²⁰⁴Pb=38.405–38.619; _Nd= +3.9 to +6.1) and generallycovary with ⁸⁷Sr/⁸⁶ Sr ratios. Radiogenic isotope data fromCrater Lake plot with published data for other Cascade volcanoeson isotope ratio correlation diagrams. The isotopic data for the Crater Lake area require sources ofprimitive magmas to consist of depleted mantle and a subductioncomponent, introduced in variable quantity to the depleted mantlewedge. Variable degrees of melting of this heterogeneous mantle,possibly at different depths, produced the diversity of isotopiccompositions and large-ion lithophile element (LILE) abundancesin primitive magmas. Trace element ratios do not indicate presenceof an ocean island basalt (OIB) source component that has beenreported in lavas of some other Cascade volcanoes. Crustal contamination may have affected isotope ratios and LILEconcentrations in evolved HAOT, where initial LILE concentrationswere low. Contamination is more difficult to detect in the calcalkalinelavas because of their higher LILE concentrations and the smallisotopic contrast with likely contaminants, such as mid- tolower-crustal rocks thought to be equivalents of igneous rocksof the Klamath Mountains and associated lower crust. Crustalassimilation appears to be required for calcalkaline rocks onlyby ¹⁸O values, which vary from lows of +5.6 to + 6.0% in HAOTand primitive basaltic andesites to a high of +7.0% in dacite,a range that is too high to be explained by plagioclase-dominatedclosed-system fractional crystallization. Elevated ¹⁸O valuesof differentiated lavas may be attributed to interaction withrelatively ¹⁸O-rich, ⁸⁷Sr-poor crustal rocks. Variably fused granitoid blocks ejected in the climactic eruption,and rarely in late Pleistocene eruptive units, have ¹⁸Opl of–3.4 to +6.5% and ¹⁸O_qz of –2.2 to +8.0% but haveSr, Nd, and Pb isotope ratios similar to volcanic rocks (e.g.⁸⁷Sr/⁸⁶Sr0.7037). Rb and Sr data for glass separates from granodioritessuggest that the source pluton is Miocene. Glass from granodioritehas ⁸⁷Sr/⁸⁶Sr ratios as high as 0.70617. Oxygen isotope fractionationbetween quartz, plagioclase, and glass indicates requilibrationof O isotopes at magmatic temperatures, after ¹⁸O/¹⁶O had beenlowered by exchange with meteoric hydrothermal fluids. Unmeltedgranodiorite xenoliths from pre-climactic eruptive units have¹⁸O values that are consistent with onset of hydrothermal exchangeearly during growth of the climactic magma chamber. Assimilationof such upper-crustal granodiorite apparently lowered ¹⁸O valuesof rhyodacites without significantly affecting their magmaticcompositions in other ways.