himu-em: The French Polynesian connection

himu, em i andem ii are three of the main geochemical mantle components that give rise to oceanic island basalts [1]. They represent the end members that produce the extreme isotopic compositions measured on intraplate volcanics. In French Polynesia, all three mantle components are represented in volcanic rocks. The characteristichimu signature is found in Tubuai, Mangaia and Rurutu,em i is present in the source of Rarotonga and Pitcairn volcanics andem ii dominates the composition of most Society Islands. Intermediate values between the three end members are found on most islands.We suggest that the three components are not independent but are physically related in the mantle. Thehimu component is thought to be recycled oceanic crust that lost part of its Pb through hydrothermal processes prior to and during subduction.em i andem ii are believed to acquire their isotopic and trace element characteristics through entrainment of sediments that were subducted together with the oceanic crust.The trace element pattern and the isotopic composition ofhimu lavas can be quantitatively modelled using a mixture of 25% old recycledmorb crust and 75% mantle peridotite. The extreme Pb composition is modelled assuming that Pb was lost from oceanic crust when hydrothermal alteration at the ridge leached Pb from the basalt to redeposit it as sulphides on top of and throughout the crust, followed by preferential dissolution of sulphides during dehydration in the subduction zone. These processes led to a drastic increase of theU/Pb ratio of the subducted material which evolved over 2 Ga to very radiogenic Pb isotopic compositions. Pb isotopic compositions similar to those ofem i andem ii are modelled assuming that sediments with average crustal Pb isotopic compositions were subducted and recycled into the mantle together with the underlyingmorb oceanic crust. Pelagic sediments (μ 5 andκ 6) account for the Pb isotopic composition ofem i whereas terrigenous sediments (μ 10 andκ 4.5) evolve towards theem ii end member. A few percent of sediment in the recycled crust-sediment mixture will destroy the characteristic Pb isotopic signature of thehimu component. This, together with the low probability of isolating oceanic crust in the mantle for 2 Ga, explains why the extremehimu composition, as seen on Tubuai and St Helena, is sampled so rarely by oceanic volcanism.     

Pb–Nd isotopic constraints on sedimentary input into the Lesser Antilles arc system

The Lesser Antilles arc is a particularly interesting island arc because it is presently very active, it is located perpendicular to the South American continent and its chemical and isotopic compositions display a strong north–south gradient. While the presence in the south of a thick pile of sedimentary material coming from the old South American continent has long been suspected to explain the geochemical gradient, previous studies failed to demonstrate unambiguously a direct link between the arc lava compositions and the subducted sediment compositions.Here, we present new Nd, Sm, Th, U and Pb concentrations and Nd–Pb isotopic data for over 60 sediments from three sites located in the fore arc region of the Lesser Antilles arc. New data for DSDP Site 543 drill core located east of Dominica Island complement the data published by White et al. [White, W.M., Dupré, B. and Vidal, P., 1985. Isotope and trace element geochemistry of sediments from the Barbados Ridge–Demerara Plain region, Atlantic Ocean. Geochimica et Cosmochimica Acta, 49: 1875–1886.] and confirm their relatively uniform isotopic compositions (i.e., ²⁰⁶Pb/²⁰⁴Pb between 19.13 and 19.53). In contrast, data obtained on DSDP Site 144 located further south, on the edge of the South American Rise and on sediments from Barbados Island are much more variable (²⁰⁶Pb/²⁰⁴Pb ranges from 18.81 to 27.69). The very radiogenic Pb isotopic compositions are found in a 60 m thick black shale unit, which has no age equivalent in the Site 543 drill core. We interpret the peculiar composition of the southern sediments as being due to two factors, (a) the proximity of the South American craton, which contributes coarse grain old detrital material that does not travel far from the continental shelf, and (b) the presence of older sediments including the thick black shale unit formed during Oceanic Anoxic events 2 and 3.The north–south isotopic change known along the Lesser Antilles arc can be explained by the observed geographical changes in the composition of the subducted sediments. About 1% contamination of the mantle wedge by Site 543 sediments explains the composition of the northern islands while up to 10% sediments like those of Site 144 is required in the source of the southern island lavas. The presence of black shales in the subducted pile provides a satisfactory explanation for the very low Δ8/4 values that characterize the Lesser Antilles arc.     

Causes of spatial compositional variations in Mariana arc lavas: Trace element evidence

New inductively coupled plasma mass spectrometry (ICP-MS) trace element data are presented on a suite of arc lavas from the northern Mariana and southern Bonin island arcs. The samples were dredged from seamounts in the Central Island Province (CIP), the Northern Seamount Province (NSP) and the Volcano Arc (VA), and they range in composition from low-K tholeiites to shoshonites. Previous studies on these samples concluded that the primary compositional control was two-component mixing between a fluid-metasomatized mid-ocean ridge basalt (MORB) source and an enriched, ocean island basalt (OIB)-like, mantle component, with subducted sediment material playing a secondary role. However, the new trace element data suggest that the compositional variations along the Mariana arc can be better explained by the addition of spatially varying subduction components to a spatially varying mantle source. The data suggest that the subduction component in the CIP and VA is dominated by aqueous fluids derived from altered oceanic crust and a pelagic sediment component, while the subduction component in the NSP is dominated by more silicic fluids derived from volcanogenic sediments as well as from pelagic sediment and altered oceanic crust. The mantle wedge in the CIP and VA is depleted relative to a normal mid-ocean ridge basalt source by loss of a small melt fraction, while the mantle wedge in the NSP is enriched either by possible gain of a small melt fraction or addition of a sediment-derived melt. Because the subduction of seamounts controls the arc and back-arc geometries, so the concomitant variation between subducted material and mantle composition may be no coincidence. The high field strength element (HFSE) data indicate a high degree of melting (∼ 25–30%) throughout the arc, ∼ 10% of which may be attributed to decompression and ∼ 20% to fluid addition.     

Oxygen- and strontium-isotopic investigations of subduction zone volcanism: the case of the Volcano Arc and the Marianas Island Arc

Recent, fresh, volcanic rocks of the intra-oceanic Mariana and Volcano Arcs were analyzed for O and Sr isotopic compositions in order to determine the source of these magmas. Fresh, non-arc, volcanic rocks from the regions surrounding the Mariana-Volcano Arcs and some DSDP sediments were also analyzed for comparison. The oxygen isotopic ratios of the arc lavas (5.5–6.8‰) exhibited a small inter-island variation that cannot be entirely explained by fractional crystallization. The Sr isotopic composition of the arc lavas is remarkably uniform (0.70332–0.70394 for the Marianas). Three models are considered in order to explain the observed isotopic characteristics: (1) bulk mixing and melting of MORB-type mantle with (a) subducted sediments, and (b) subducted oceanic crust (excluding sediments); (2) melting of a mixture of sediment-derived fluids and MORB-type mantle; and (3) melting of a mixture of sediment-derived fluids and oceanic island or “hot-spot” type mantle. The last model fits the data best. The conclusion that very small, and variable, amounts of sediment-derived fluid ( 1%) are required to explain the observed inter-island O isotopic variation, is consistent with that of other workers who used different isotopic and trace element methods. The generation of magmas in the Mariana-Volcano Arcs involves very little sediment and the source region of Mariana lavas is isotopically indistinguishable from that of hot-spot basalts.     

Pb isotopes in Ascension Island rocks: oceanic origin for the gabbroic to granitic plutonic xenoliths

The Pb isotopic compositions and U and Pb concentrations of the lava series (alkali basalt to comendite) and of their plutonic xenoliths (gabbro to alkaline granite) of Ascension Island are reported. The data are used to evaluate the source of the xenoliths which formed two differentiation suites: the acidic and intermediate xenoliths together with most of the lavas on the one hand, and the gabbroic xenoliths and a basaltic tuff on the other hand. The Pb isotopic compositions imply a mantle origin for the source magmas of the xenoliths and confirm the possibility of generating granitic rocks in an oceanic environment by fractional crystallization of a mantle-derived magma whose geochemical and isotopic characteristics are comparable to the source magmas of oceanic island basalts.     

Aleutian magnesian andesites: Melts from subducted Pacific ocean crust

Several diagnostic chemical characteristics of an uncommon Aleutian magma type support a proposed origin that involves a small amount of partial melting of subducted Pacific ocean crust (basalt) consisting mainly of garnet and clinopyroxene (eclogite or garnet websterite). Among the characteristics are high La/Yb ratios and Sr contents and low ratios of radiogenic to non-radiogenic Sr and Pb. The major element composition of the andesites resembles that of hydrous melts in equilibrium with peridotite: a low ratio of total Fe to Mg is distinctive. These disparate observations can be reconciled if large ion lithophile (LIL)- element-rich hydrous melt from the subducted oceanic crust equilibrates with olivine and orthopyroxene in overlying LIL-element-depleted mantle and then erupts without interacting with the island are crust. The compositional dissimilarity of the magnesian andesites and most other andesites from the Aleutian island arc precludes application of this model to island are magmatism in general.     

Siderophile and chalcophile element abundances in oceanic basalts, Pb isotope evolution and growth of the Earth''s core

We have investigated the hypothesis that mantle Pb isotope ratios reflect continued extraction of Pb into the Earth's core over geologic time. The Pb, Sr and Nd isotopic compositions, and the abundance of siderophile and chalcophile elements (W, Mo and Pb) and incompatible lithophile elements have been determined for a suite of ocean island and mid-ocean ridge basalt samples. Over the observed range in Pb isotopic compositions for oceanic rocks, we found no systematic variation of siderophile or chalcophile element abundances relative to abundances of similarly incompatible, but lithophile, elements. The high sensitivity of theMo/Pr ratio to segregation of Fe-metal or S-rich metallic liquid (sulfide) and the observed constantMo/Pr ratio rules out the core formation model as an explanation for the Pb paradox. The mantle and crust have the sameMo/Pr and the sameW/Ba ratios, suggesting that these ratios reflect the ratio in the Earth's primitive mantle.

Our data also indicate that thePb/Ce ratio of the mantle is essentially constant, but the presentPb/Ce ratio in the mantle ( 0.036) is too low to represent the primitive value ( 0.1) derived from Pb isotope systematics. HigherPb/Ce ratios in the crust balance the lowPb/Ce of the mantle, and crust and mantle appear to sum to a reasonable terrestrialPb/Ce ratio. The constancy of thePb/Ce ratio in a wide variety of oceanic magma types from diverse mantle reservoirs indicates this ratio is not fractionated by magmatic processes. This suggests crust formation must have involved non-magmatic as well as magmatic processes. Hydrothermal activity at mid-ocean ridges may result in significant non-magmatic transport of Pb from mantle to crust and of U from crust to mantle, producing a higherU/Pb ratio in the mantle than in the total crust. We suggest that the lower crust is highly depleted in U and has unradiogenic Pb isotope ratios which balance the radiogenic Pb of upper crust and upper mantle. The differences between thePb/Ce ratio in sediments, this ratio in primitive mantle, and the observed ratio in oceanic basalts preclude both sediment recycling and mixing of primitive and depleted reservoirs from being important sources of chemical heterogeneities in the mantle.     

The influence of crustal structure on compositions of subduction-related magmas

A survey of Sr isotopic ratios and other compositional features of subduction-related magma suites reveals significant correlations between these averaged parameters and characteristics of the underlying crust (i.e., thickness, composition, and age). These observations lead to the conclusion that crust and(or) mantle rocks in the hanging walls of subduction zones are involved in modification of primary mafic magmas (typically basalt or basaltic andesite). It is proposed that mafic magmas will stagnate within the crust or uppermost mantle where they may differentiate and react with wall rocks. The extent to which such processes manifest themselves will depend upon details of the local crustal structure. In particular, the composition and age of the crust will strongly influence such parameters as Sr, Nd and Pb isotopic compositions. Such data strongly indicate the involvement of crustal rocks in locales underlain by old sialic crust (e.g., central Andes). Depending upon the level of magma stagnation and evolution within the crust, different trends in isotopic composition may result. These isotopic trends may be enhanced by partial melting of the wall rocks to produce relatively silicic anatectic magmas, and locally they may reflect subduction of continental sediments. Interpretation of the isotopic data may be more ambiguous in locales underlain by younger and more mafic continental crust (Cascades, E Eleutians) and those underlain by oceanic crust owing to the similarity in isotopic composition of primary magmas and the latter crustal materials. Yet some degree of crustal involvement in magmatic evolution seems highly probable even in these more primitive terranes. Consequently, most island arc magmas, and especially those more evolved than basalt, are probably not primary in the sense that they do not represent direct melts of the upper mantle. Studies of arc volcanic rocks may yield misleading conclusions concerning processes of magma generation related to subduction unless evolutionary processes are defined and their effects considered. It appears that modern volcanic arcs provide a poor analog for models of early crustal development because the modern mantle-derived magmatic components are more mafic in composition than average continental crust.     

Fukutoku-oka-no-ba Volcano: A new perspective on the Alkalic Volcano Province in the Izu–Bonin – Mariana arc

Pumice samples from Fukutoku-oka-no-ba in the Izu–Bonin – Mariana (IBM) arc were analysed for 40 trace elements and Sr, Nd, and Pb isotopic compositions. These samples are shoshonites (59.4–61.8 wt% SiO₂), characterized by high contents of K₂O (3.74–4.64 wt%), Ba (1274–1540 p.p.m.), Rb (91–105 p.p.m.), and light rare earth elements. The characteristics of alkali-element enrichment are similar to those of other parts of the Alkalic Volcano Province (AVP) in the northern Mariana and southernmost Volcano arcs. Sr (⁸⁷Sr/⁸⁶Sr = 0.7036–0.7038) and Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb = 19.08–19.11, ²⁰⁷Pb/²⁰⁴Pb = 15.62–15.63, ²⁰⁸Pb/²⁰⁴Pb = 38.85–38.91) of Fukutoku-oka-no-ba pumice are relatively radiogenic, whereas Nd is unradiogenic (¹⁴³Nd/¹⁴⁴Nd = 0.51283–0.51286). Fukutoku-oka-no-ba is isotopically distinct from Iwo Jima and is similar to the Hiyoshi Volcanic Complex, suggesting that Fukutoku-oka-no-ba might have a magma source similar to that of the Hiyoshi volcanic complex. Plots of Pb and Nd isotopes for AVP lavas trend toward the fields of ocean island basalt (OIB) source and pelagic sediments, which are possible sources of AVP enrichments.     

Identification of recycled continental material in the mantle from Sr,Nd and Pb isotope investigations

Pb, Nd and Sr isotope compositions of oceanic basalts have been used to identify recycled components of continent derivation in the mantle. The isotopic compositions of Sr, Nd and Pb, together with U, Pb, Sm, Nd, Rb, and Sr abundances have been determined for back-arc basalt glasses from the Scotia Sea and Parece Vela and West Philippine Basins, in addition to basalts from South Sandwich Islands, Ascension, St. Helena and Tristan da Cunha. Comparisons made between the isotopic compositions of South Sandwich Islands basalts and Atlantic MORB glasses permit the identification of recycled components of continent derivation in the source of the island arc basalts. Recycled Sr of continent derivation is also recognisable in back-arc basalt glasses from the Scotia Sea and Parece Vela and West Philippine Basins. However, contemporary reinjection of material with the isotopic structures similar to those identified as a component of island arc and back-arc regions cannot be the sole or dominant influence on the fine structure observed in MORB glasses from the Atlantic Ocean, nor the isotopic compositions of Tristan da Cunha, St. Helena and Ascension basalts. Recycled materials are likely to have been responsible for the generation of these heterogeneities only if they have been stored in the mantle for periods of time exceeding 10⁹ years.     

Across-arc geochemical variation of Quaternary lavas in West Java, Indonesia: Mass-balance elucidation using arc basalt simulator model

The Sunda Arc of Indonesia developed along the convergent margin between the Eurasian and the Australian Plates. More than 100 Quaternary volcanic centers occur along the arc. The West Java Arc is a segment of the Sunda Arc in which more than 10 volcanic centers are located, corresponding to the 120 to 200 km depth contours of the Wadati–Benioff zone. The geochemistry of 207 Quaternary lavas from six centers across the arc was investigated. The lavas range from basalt to dacite. Incompatible element abundances increase from the volcanic front to the rear‐arc in response to a change from low‐K to high‐K suites. Nd–Sr isotope compositions of the basalts scatter between mid‐ocean ridge basalt (MORB) source mantle and Indian Ocean sediment (SED) compositions, with volcanic front low‐K basalts having more radiogenic Nd than the rear‐arc basalts. It is suggested that mixing between slab‐derived fluids mainly from the SED and melt from MORB source mantle played a significant role in determining the geochemistry of the West Java basalts. Incompatible element patterns in primitive mantle normalized multi‐element plots are almost identical across the arc, except for greater inclination and weaker positive Sr spikes in the rear‐arc basalts. This suggests a lower degree of partial melting in the rear‐arc mantle, accompanied by change in SED fluid composition between the volcanic front and the rear‐arc. The latter is confirmed by fluid‐fluxed melting model calculations using multiple trace elements and Nd and Sr isotopes. All the West Java Arc lavas require deficit of Sr from the slab SED. This may occur due to selective breakdown of Sr‐rich hydrous silicate minerals, such as zoisite, at shallower depths before the SED component reaches the depth of dehydration effective for magma genesis. The rear‐arc basalts need further Sr deficits along with lesser fluid. These features are commonly observed in many arc basalts, and are likely attributable to the same mechanism.     

Trace element behavior in hydrothermal experiments: Implications for fluid processes at shallow depths in subduction zones

Chemical evaluation of fluids affected during progressive water-sediment interactions provides critical information regarding the role of slab dehydration and/or crustal recycling in subduction zones. To place some constraints on geochemical processes during sediment subduction, reactions between décollement sediments and synthetic NaCl-CaCl₂ solutions at 25–350°C and 800 bar were monitored in laboratory hydrothermal experiments using an autoclave apparatus. This is the first attempt in a single set of experiments to investigate the relative mobilities of many subduction zone volatiles and trace elements but, because of difficulties in conducting hydrothermal experiments on sediments at high P-T conditions, the experiments could only be designed for a shallow ( 10 km) depth. The experimental results demonstrate mobilization of volatiles (B and NH₄) and incompatible elements (As, Be, Cs, Li, Pb, Rb) in hydrothermal fluids at relatively low temperatures ( 300°C). In addition, a limited fractionation of light from heavy rare earth elements (REEs) occurs under hydrothermal conditions. On the other hand, the high field strength elements (HFSEs) Cr, Hf, Nb, Ta, Ti, and Zr are not mobile in the reacted fluids. The observed behavior of volatiles and trace elements in hydrothermal fluids is similar to the observed enrichment in As, B, Cs, Li, Pb, Rb, and light REEs and depletion in HFSEs in arc magmas relative to magmas derived directly from the upper mantle. Thus, our work suggests a link between relative mobilities of trace elements in hydrothermal fluids and deep arc magma generation in subduction zones. The experimental results are highly consistent with the proposal that the addition of subduction zone hydrous fluids to the subarc mantle, which has been depleted by previous melting events, can produce the unique characteristics of arc magmas. Moreover, the results suggest that deeply subducted sediments may no longer have the composition necessary to generate the other distinct characteristics, such as the B-δ¹¹ B and B-¹⁰Be systematics, of arc lavas. Finally, the mobilization of B, Cs, Pb, and light REEs relative to heavy REEs in the hydrothermal fluids fractionate the ratios of B/Be, B/Nb, Cs/Rb, Pb/Ce, La/Ba and LREE/HREE, which behave conservatively during normal magmatic processes. These results demonstrate that the composition of slab-derived fluids has great implications for the recycling of elements; not only in arc magmas but also in mantle plumes.     

Fine-scale isotopic variation in Mariana Trough basalts: evidence for heterogeneity and a recycled component in backarc basin mantle

Fine-scale sampling with alvin and by dredging of the axial ridge in the Mariana Trough between 17°40′N and 18°30°N recovered basalts with isotopic compositions that span the range between N-type MORB and Mariana island arc basalts. There is a local tectonic-morphological control on basalt compositions; MORB-like basalts are found on the deeper ridge segment bounded by the Pagan transform and the ridge offset at 17°56′N, while basalts from the shallower ridge to the north are typical Mariana Trough basalts (MTB) having compositions intermediate between the two endmember rock types. Arc-like basalts were recovered from one site on the axial ridge.The discovery of basalts with such diverse isotopic characteristics from a short (100 km) section of this backarc spreading center constrains the chemical characteristics and distribution of mantle source variability in the Mariana Trough. SrNdPb isotopic variability suggests that the MTB source is heterogeneous on the scale of individual melt batches. The principal component in the MTB mantle source region is depleted peridotite similar to the source of MORB. The enriched component, most evident in the arc-like basalts and intimately mixed in MTB, has isotopic characteristics similar to those observed in the Mariana arc basalts. The isotopic data suggest that source variability for Mariana axial ridge basalts can be explained by mixed arc-like and MORB-like mantle. We hypothesize that there are fragments of old oceanic lithosphere in the backarc source region. This lithospheric component may reflect remnants of subducted seafloor or forearc-volcanic arc mantle that predate rifting in the backarc basin.     

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

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

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

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

Did boninite originate from the heterogeneous mantle with recycled ancient slab?

Boninites are widely distributed along the western margin of the Pacific Plate extruded during the incipient stage of the subduction zone development in the early Paleogene period. This paper discusses the genetic relationships of boninite and antecedent protoarc basalt magmas and demonstrates their recycled ancient slab origin based on the T–P conditions and Pb–Hf–Nd–Os isotopic modeling. Primitive melt inclusions in chrome spinel from Ogasawara and Guam islands show severely depleted high‐SiO₂, MgO (high‐silica) and less depleted low‐SiO₂, MgO (low‐silica and ultralow‐silica) boninitic compositions. The genetic conditions of 1 346 °C at 0.58 GPa and 1 292 °C at 0.69 GPa for the low‐ and ultralow‐silica boninite magmas lie on adiabatic melting paths of depleted mid‐ocean ridge basalt mantle with a potential temperature of 1 430 °C in Ogasawara and of 1 370 °C in Guam, respectively. This is consistent with the model that the low‐ and ultralow‐silica boninites were produced by remelting of the residue of the protoarc basalt during the forearc spreading immediately following the subduction initiation. In contrast, the genetic conditions of 1 428 °C and 0.96 GPa for the high‐silica boninite magma is reconciled with the ascent of more depleted harzburgitic source which pre‐existed below the Izu–Ogasawara–Mariana forearc region before the subduction started. Mixing calculations based on the Pb–Nd–Hf isotopic data for the Mariana protoarc basalt and boninites support the above remelting model for the (ultra)low‐silica boninite and the discrete harzburgite source for the high‐silica boninite. Yb–Os isotopic modeling of the high‐Si boninite source indicates 18–30 wt% melting of the primitive upper mantle at 1.5–1.7 Ga, whereas the source mantle of the protoarc basalt, the residue of which became the source of the (ultra)low‐Si boninite, experienced only 3.5–4.0 wt% melt depletion at 3.6–3.1 Ga, much earlier than the average depleted mid‐ocean ridge basalt mantle with similar degrees of melt depletion at 2.6–2.2 Ga.     

Cenozoic volcanism and lithospheric tectonic evolution in Qiangtang area, northern Qinghai-Tibet Plateau

Accompanying with the shortening,thickening and uplifting of the lithosphere,a series of Cenozoic potassic volcanic rock zones are developed in the northern Qinghai-Tibet Plateau.From south to north,the volcanic rocks can be divided into three volcanicrock belts:Qiangtang-Nangqian volcanic belt,Middle Kunlun-Hoh Xil volcanic belt and Western Kunlun-Eastern Kunlun volcanic belt[1].Spatiotemporal evolu-tion of the volcanism and the origins of magmas con-strains on the pulsing uplifting and …     

Geochemistry and petrogenesis of the Cretaceous A‐type granites in the Laoshan granitic complex,eastern China

Major element and trace element compositions, and Sr, Nd and Pb isotopic compositions for postcollisional granites from the Laoshan granitic complex, in the eastern side of the Triassic suture between the South China and North China tectonic blocks were determined. The granites are alkaline, A‐type and can be further classified as A1 granites. The trace element composition of these granites is transitional between those of oceanic island basalt and enriched mid‐oceanic ridge basalt, with depletions in Ba, Sr, P, and Ti that can be ascribed to mineral fractionation and enrichments in Cs, Rb, Th and U possibly resulted from the involvement of slab fluids. The isotopic signature of Laoshan granites represent a mixture between an enriched mantle type 1 (EMI)‐like end‐member and lower continental crust (LCC). We propose that the magmas that formed the Laoshan A1 granites are a mixture between those derived from the EMI‐like delaminated eclogitic rocks (subsequently enriched by fluids released from Mesozoic Pacific subducted slab) and those derived from the LCC, which consists of granulites or metamorphic residues from the prior generation of I‐type granites in the region. The mixed magmas then experienced a strongly alkali feldspar‐dominated fractionation prior to their emplacements as A‐type granites in the Laoshan granitic complex.     

Petrologic evolution of Palau,a nascent island arc

Palau Islands, 7°30′N, are the only emergent feature on the more than 2500‐km‐long Kyushu–Palau Ridge. Small islands are mainly uplifted reef carbonate. Larger islands are volcanic with basalt to dacite and rare boninite. Polymict breccia is abundant: sills, flows, and dykes are common but pillows are rare. Palau Trench samples include all types found on the islands as well as high‐Mg basalt. Volcanism began in the late Eocene and ended by early Miocene. All igneous rocks comprise a low‐K primitive island arc‐tholeiite series. None are mid‐ocean ridge basalts. Rare earth elements and high field‐strength elements indicate a depleted mantle source. Elevated large ion lithophile elements and light rare earth elements indicate influx of ‘dehydration fluid’. Ce/Ce* and Eu/Eu* ratios show no evidence for recycling of arc‐derived clastics. Plate reconstructions and paleomagnetic data suggest that the arc probably formed on the trace of a transform fault that migrated northward and rotated clockwise up to 90°. Episodes of transtension caused upwelling of hot mantle into depleted mantle and sheared altered rocks of the transform. Episodes of transpression may have initiated subduction of old seafloor with a thin cover of pelagic sediments deposited far from terrigenous sediment sources.     

Flux versus decompression melting at stratovolcanoes in southeastern Guatemala

The major and trace element geochemistry of lavas erupted from four volcanic front (VF) stratovolcanoes in southeastern Guatemala show differences in the relative importance of flux and decompression melting in a continental arc setting. The VF stratovolcanoes exhibit a wide compositional range from basalt to dacite, although modern Pacaya erupts basaltic lavas. The VF basalts have relatively low MgO contents and plot outside the field of primary arc magmas defined by melting experiments on hydrous peridotite. After subtracting the effects of the fractionation, assimilation, and alteration of some VF lavas, separate partial melting and mixing trends were identified for Agua–Pacaya and Tecuamburro–Moyuta.The distinct chemical signatures of the hemipelagic and carbonate sediments subducted off Guatemala provide constraints on material transfer processes that occurred between the slab and mantle wedge. Model fluids and melts from the subducted slab were calculated using recently published mineral–aqueous fluid partition coefficients. Wide separation of the model fluid and melt compositions on a U/La versus Ba/Th diagram creates diagnostic mixing curves with an enriched mid-ocean ridge basalt source. Fluid from mature ocean crust has high U/La, fluid from carbonate sediment has high Ba/Th, and fluid and melt from hemipelagic sediments have both high U/La and Ba/Th. In a simple single-stage model, a mantle metasomatized by fluid originating largely from the oceanic crust with only minor sediment fluid contributions best explains the overall large ion lithophile element composition of the VF lavas. (Th/Rb)_N ratios of ∼1 in the VF lavas from southeastern Guatemala require a component of sediment melting. Therefore, a more realistic two-stage model to describe the Guatemalan arc data involves an initial hemipelagic sediment melt input to the wedge followed by minor fluid additions from the oceanic crust or sediments. Correlation between measures of slab input and extent of melting in the older VF lavas from Tecuamburro and Moyuta favors flux-dominated melting near the base of the mantle wedge. In sharp contrast, the lack of a relationship between slab additions and melting in younger lavas from Agua and Pacaya volcanoes implies a significant role for decompression melting closer to the top of the wedge. In this melting scenario, the rate of crustal extension determines the extent of melting.