Small-scale coexistence of island-arc- and enriched-MORB-type basalts in the central Vanuatu arc

We report here major, trace element and Sr–Nd–Pb isotopic data for a new set of basaltic lavas and melt inclusions hosted in Mg-rich olivines (Fo_86–91) from Mota Lava, in the Banks islands of the Vanuatu island arc. The results reveal the small-scale coexistence of typical island-arc basalts (IAB) and a distinct type of Nb-enriched basalts (NEB) characterized by primitive mantle-normalized trace element patterns without high-field-strength element (HFSE) depletion. The IAB show trace element patterns with prominent negative HFSE anomalies acquired during melting of mantle sources enriched with slab-derived, H₂O-rich components during subduction. In contrast, the NEB display trace element features that compare favourably with enriched-mid-ocean ridge basalt (MORB) and the most enriched basalts from the Vanuatu back-arc troughs. Both their trace element and Nd–Sr isotopic compositions require partial melting of an enriched-MORB-type mantle source, almost negligibly contaminated by slab-derived fluids (~0.2 wt%). The coexistence of these two distinct types of primitive magma, at the scale of one volcanic island and within a relatively short span of time, would reflect a heterogeneous mantle source and/or tapping of distinct mantle sources. Direct ascent of such distinct magmas could be favoured by the extensive tectonic setting of Mota Lava Island, allowing decompression melting and sampling of variable mantle sources. Significantly, this island is located at the junction of the N–S back-arc troughs and the E–W Hazel Home extensional zone, where the plate motion diverges in both direction and rate. More broadly, this study indicates that crustal faulting in arc contexts would permit basaltic magmas to reach Earth’s surface, while preserving the geochemical heterogeneity of their mantle sources.     

Assessing subcontinental lithospheric mantle sources for basalts: Neogene volcanism in the Pacific Northwest,USA as a test case

Many objections have been raised as to the ability of subcontinental lithospheric mantle to produce voluminous amounts of basalt, because this upper part of the mantle is thought to be refractory, and the geotherm is rarely above the peridotite solidus at these depths under continents. However, in the Pacific Northwest of the USA during the Neogene, the subcontinental lithospehric mantle has been proposed as a key source for basalts erupted within the northern Basin and Range, and for the Columbia River flood basalts erupted on the Columbia Plateau. An alternative explanation to melting in the subcontinental lithospheric mantle, which equally well explains the chemical compositions thought to originate there, is that these magmas were contaminated by crust of varying ages. Calc-alkaline lavas, which occupy the Blue Mountains in the center of this region, hold clues to the latter process. Their elevated trace element ratios (e.g., Ba/Zr, K₂O/P₂O₅), coupled with differentiation indicators such as Mg? [molar Mg/(Mg?+?Fe)], and Sr, Nd, and Pb isotopic compositions, can most reasonably be explained by crustal contamination. Appraisal of continental peridotite xenolith data indicates that high trace element ratios such as Ba/Zr in continental basalts cannot result from melting in the subcontinental lithospheric mantle. Instead, as with the calc-alkaline lavas, these high ratios in the tholeiites most likely indicate crustal contamination. Furthermore, the peridotite xenoliths do not have a relative depletion in Nb and Ta that is observed in most of the lavas within the region. Relatively minor volumes of tholeiites erupted in late Neogene times in the northern Basin and Range (Hi-Mg olivine tholeiites) and Columbia Plateau (Saddle Mountains basalts), are the only lavas which have trace element and isotopic compositions consistent with being derived from, or largely interacting with a subcontinental lithospheric mantle in the Pacific Northwest. In contrast to the prior studies, we suggest that the mantle sources for most of the basalts in this region were ultimately beneath the lithospheric mantle.     

Petrology of peridotite xenolith-bearing basaltic to andesitic lavas from the Shiribeshi Seamount,off northwestern Hokkaido,the Sea of Japan

The Shiribeshi Seamount off northwestern Hokkaido, the Sea of Japan, is a rear-arc volcano in the Northeast Japan arc. This seamount is composed of calc-alkaline and high-K basaltic to andesitic lavas containing magnesian olivine phenocrysts and mantle peridotite xenoliths. Petrographic and geochemical characteristics of the andesite lavas indicate evidence for the reaction with the mantle peridotite xenoliths and magma mixing between mafic and felsic magmas. Geochemical modelling shows that the felsic end-member was possibly derived from melting of an amphibolitic mafic crust. Chemical compositions of the olivine phenocrysts and their chromian spinel inclusions indicate that the Shiribeshi Seamount basalts in this study was derived from a primary magma in equilibrium with relatively fertile mantle peridotites, which possibly represents the mafic end-member of the magma mixing. Trace-element and REE data indicate that the basalts were produced by low degree of partial melting of garnet-bearing lherzolitic source. Preliminary results from the mantle peridotite xenoliths indicate that they were probably originated from the mantle beneath the Sea of Japan rather than beneath the Northeast Japan arc.     

Magmatic source enrichment by slab-derived melts in a young post-collision setting, central Mindanao (Philippines)

Central Mindanao was the locus of a Pliocene (4–5 Ma old) arc–arc collision event followed by basaltic to dacitic magmatism starting at 2.3 Ma, representing the most voluminous volcanic field in the Philippines. Lava compositions range from calc-alkaline to shoshonitic. Adakites and Nb-enriched basalts are among the magmatic products. All the lavas are Na-rich (up to 4.88%), with Na₂O/K₂O ratios from 2.5 to 6.5. Sr, Nd and Pb isotopic compositions are similar to MORB, except for some shoshonitic lavas that have slightly less radiogenic Nd ratios. K-enrichment in basalts can be related to both fractional crystallization (FC) at moderate pressures and to partial melting of an enriched source. Trace element systematics indicate that the sub-central Mindanao mantle is characterized by the presence of garnet, phlogopite, amphibole, and perhaps some titanate phase. The enrichment of this source is attributed to the interaction of slab-derived melts, i.e., adakites, with the arc mantle. This would explain the presence of Nb-enriched basalts, transitional adakites and high-magnesium andesites, as well as the bulk Na-enrichment and relatively unradiogenic character of the central Mindanao lavas. We envision an ion-exchange type of enrichment, in which the HFSE, LILE and LREE, mobilized during slab melting, are preferentially enriched in the metasomatized mantle, resulting in a diversity of post-collision magma compositions. The MORB-like isotopic signatures of the central Mindanao lavas preclude important contributions of slab-derived hydrous fluids, sediments, continental crust or an OIB-type contaminant. Slab melting after cessation of subduction is deemed possible by thermal rebound of previously depressed geotherms. Initial contributions to mantle enrichment in post-collision sites may thus come from slab melts. In most other cases of post-collision magmatism, however, this signature can be easily masked by enrichments coming from other sources, e.g., the continental lithosphere.     

Isotopic and trace element constraints on the petrogenesis of lavas from the Mount Adams volcanic field,Washington

Strontium, Nd, Pb, Hf, Os, and O isotope compositions for 30 Quaternary lava flows from the Mount Adams stratovolcano and its basaltic periphery in the Cascade arc, southern Washington, USA indicate a major component from intraplate mantle sources, a relatively small subduction component, and interaction with young mafic crust at depth. Major- and trace-element patterns for Mount Adams lavas are distinct from the rear-arc Simcoe volcanic field and other nearby volcanic centers in the Cascade arc such as Mount St. Helens. Radiogenic isotope (Sr, Nd, Pb, and Hf) compositions do not correlate with geochemical indicators of slab-fluids such as (Sr/P) _n and Ba/Nb. Mass-balance modeling calculations, coupled with trace-element and isotopic data, indicate that although the mantle source for the calc-alkaline Adams basalts has been modified with a fluid derived from subducted sediment, the extent of modification is significantly less than what is documented in the southern Cascades. The isotopic and trace-element compositions of most Mount Adams lavas require the presence of enriched and depleted mantle sources, and based on volume-weighted chemical and isotopic compositions for Mount Adams lavas through time, an intraplate mantle source contributed the major magmatic mass of the system. Generation of basaltic andesites to dacites at Mount Adams occurred by assimilation and fractional crystallization in the lower crust, but wholesale crustal melting did not occur. Most lavas have Tb/Yb ratios that are significantly higher than those of MORB, which is consistent with partial melting of the mantle in the presence of residual garnet. δ ¹⁸O values for olivine phenocrysts in Mount Adams lavas are within the range of typical upper mantle peridotites, precluding involvement of upper crustal sedimentary material or accreted terrane during magma ascent. The restricted Nd and Hf isotope compositions of Mount Adams lavas indicate that these isotope systems are insensitive to crustal interaction in this juvenile arc, in stark contrast to Os isotopes, which are highly sensitive to interaction with young, mafic material in the lower crust.     

Secular Geochemistry of Central Puerto Rican Island Arc Lavas: Constraints on Mesozoic Tectonism in the Eastern Greater Antilles

Island arc volcanism in the Greater Antilles persisted for >70m.y. from Middle Cretaceous to Late Eocene time. During theinitial 50 m.y., lavas in central Puerto Rico shifted from predominantlyisland arc tholeiites (volcanic phase I, Aptian to Early Albian,120–105 Ma), to calc-alkaline basalts (phase II, LateAlbian, 105–97 Ma), and finally to high-K, incompatible-element-enrichedbasalts (phases III and IV, Cenomanian–Maastrichtian,97–70 Ma). Following an island-wide eruptive hiatus, geochemicaltrends were reversed in the Eocene with renewed eruption ofcalc-alkaline basalts (phase V, 60–45 Ma). Progressiveincreases in large-ion lithophile elements (LILE)/light rareearth elements (LREE), LILE/high field strength elements (HFSE),LREE/HFSE, and HFSE/heavy rare earth elements (HREE) characterizethe compositional evolution of the first four volcanic phases.The shift in trace element compositions is mirrored by increasingradiogenic content of the lavas. Pb     

Calc-alkaline, Shoshonitic, and Primitive Tholeiitic Lavas from Monogenetic Volcanoes near Crater Lake, Oregon

Quaternary monogenetic volcanism in the High Cascades of Oregonis manifested by cinder cones, lava fields, and small shields.Near Crater Lake caldera, monogenetic lava compositions include:low-K (as low as 0?09% K₂O) high-alumina olivine tholeiite (HAOT);medium-K. calc-alkaline basalt, basaltic andesite, and andesite;and shoshonitic basaltic andesite (2?1% K₂O, 1750 ppm Sr at54% SiO₂). Tholeiites have MORB-like trace element abundancesexcept for elevated Sr, Ba, and Th and low high field strengthelements (HFSE), and they represent near-primary liquids. Theyare similar to HAOTs from the Cascades and adjacent Basin andRange, and to many primitive basalts from intraoceanic arcs.Calc-alkaline lavas show a well-developed arc signature of highlarge-ion lithophile elements (LILE) and low HFSE. Their Zrand Hf concentrations are at least partly decoupled from thoseof Nb and Ta; HREE are low relative to HAOT. Incompatible elementabundances and ratios vary widely among basaltic andesites.Some calc-alkaline lavas vented near Mount Mazama contain abundantgabbroic microxcnoliths, and are basaltic andesitic magmas contaminatedwith olivine gabbro. A calc-alkaline basalt and a few basaltic andesites have MgOand compatible trace element contents that suggest only minorfractionation. There appears to be a compositional continuumbetween primitive tholeiitic and calc-alkaline lavas. Compositionalvariation within suites of comagmatic primitive lavas, boththoleiitic and calc-alkaline, mainly results from differentdegrees of partial melting. Sources of calc-alkaline primarymagmas were enriched in LILE and LREE by a subduction componentand contained residual garnet, whereas sources of HAOTs hadlower LILE and LREE concentrations and contained residual clinopyroxene.High and variable LILE and LREE contents of calc-alkaline lavasreflect variations in fluid-transported subduction componentadded to the mantle wedge, degree of partial melting, and possiblyalso interaction with rocks or partial melts in the lower crust. Andesites were derived from calc-alkaline basaltic andesitesby fractionation of plagioclase+augite+magnetite+apatite ? orthopyroxeneor olivine, commonly accompanied by assimilation. Many andesitesare mixtures of andesitic or dacitic magma and a basaltic orbasaltic andesitic component, or are contaminated with gabbroicmaterial. Mingled basalt, andesite, and dacite of Williams Craterformed by multi-component, multi-stage mixing of basaltic andesiticmagma, gabbro, and dacitic magma. The wide range of compositionsvented from monogenetic volcanoes near Crater Lake is a resultof the thick crust coupled with mild tectonic extension superimposedon a subduction-related magmatic arc.     

Subduction zone geochemistry

Crustal recycling at convergent plate boundaries is essential to mantle heterogeneity.However,crustal signatures in the mantle source of basaltic rocks above subduction zones were primarily incorporated in the form of liquid rather than solid phases.The physicochemical property of liquid phases is determined by the dehydration behavior of crustal rocks at the slab-mantle interface in subduction channels.Because of the significant fractionation in incompatible trace elements but the full inheritance in radiogenic isotopes relative to their crustal sources,the production of liquid phases is crucial to the geochemical transfer from the subducting crust into the mantle.In this process,the stability of specific minerals in subducting crustal rocks exerts a primary control on the enrichment of given trace elements in the liquid phases.For this reason,geochemically enriched oceanic basalts can be categorized into two types in terms of their trace element distribution patterns in the primitive mantle-normalized diagram.One is island arc basalts(IAB),showing enrichment in LILE,Pb and LREE but depletion in HFSE such as Nb and Ta relative to HREE,The other is ocean island basalts(OIB),exhibiting enrichment in LILE and LREE,enrichment or non-depletion in HFSE but depletion in Pb relative to HREE.In either types,these basalts show the enhanced enrichment of LILE and LREE with increasing their incompatibility relative to normal mid-ocean ridge basalts(MORB).The thermal regime of subduction zones can be categorized into two stages in both time and space,The first stage is characterized by compressional tectonism at low thermal gradients.As a consequence,metamorphic dehydration of the subducting crust prevails at forearc to subarc depths due to the breakdown of hydrous minerals such as mica and amphibole in the stability field of garnet and rutile,resulting in the liberation of aqueous solutions with the trace element composition that is considerably enriched in LILE,Pb and LREE but depleted in HFSE and HREE relative to normal MORB.This provides the crustal signature for the mantle sources of IAB.The second stage is indicated by extensional tectonism at high thermal gradients,leading to the partial melting of metamorphically dehydrated crustal rocks at subarc to postarc depths.This involves not only the breakdown of hydrous minerals such as amphibole,phengite and allanite in the stability field of garnet but also the dissolution of rutile into hydrous melts.As such,the hydrous melts can acquire the trace element composition that is significantly enriched in LILE,HFSE and LREE but depleted in Pb and HREE relative to normal MORB,providing the crustal signature for the mantle sources of OIB.In either case,these liquid phases would metasomatize the overlying mantle wedge peridotite at different depths,generating ultramafic metasomatites such as serpentinized and chloritized peridotites,and olivine-poor pyroxenites and hornblendites.As a consequence,the crustal signatures are transferred by the liquid phases from the subducting slab into the mantle.     

Isotopic constraints on time scales and mechanisms of slab material transport in the mantle wedge: evidence from the Simcoe mantle xenoliths, Washington, USA

Spinel harzburgite and websterite mantle xenoliths from Simcoe volcano in southern Washington represent fragments of mantle lithosphere from the back-arc side of the Cascade arc front. Previous studies have shown that metasomatism by either silica-rich fluids or hydrous melts crystallized phlogopite, imparted high oxygen fugacities (0.3 to 1.4 log units above QFM), and more radiogenic Os isotopic compositions on these peridotites. These features are consistent with part or all of the metasomatic agent being derived from the Juan de Fuca slab. New Re–Os, Sm–Nd, Sr, and U–Th–Pb isotopic data shed further light on the origin and composition of the metasomatic agent. The clinopyroxenes from the xenoliths have correlated Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb=18.63–19.55, ²⁰⁷Pb/²⁰⁴Pb=15.56–15.63, ²⁰⁸Pb/²⁰⁴Pb=38.22–38.87). The most radiogenic Pb isotopic compositions extend beyond the most radiogenic Pb isotopic compositions for the Cascade arc lavas and display a shallower trend. Mixtures between Juan de Fuca basalts and pelagic or terrigenous sediments would result in Pb isotopic compositions that are not radiogenic enough in ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb at the high ²⁰⁶Pb/²⁰⁴Pb end of this array. Therefore, models for rapid transfer of components from the slab to the mantle lithosphere are not viable in this case. Instead, a multi-stage model is preferred. In the first stage, the slab component is transferred via fluid or melt into, and reacts with the hanging wall mantle. This results in a residual slab depleted in Pb relative to U and Th, and consequent high U/Pb and Th/Pb. Additional dehydration or melting of the slab imparts this chemical signature to the peridotite in the hanging wall. In the second stage, the hybridized hanging wall peridotite evolves for tens of million years until corner flow drags it down to deeper levels in the mantle wedge where melting occurs in response to higher temperatures. In the third stage, this melt migrates upward where it metasomatizes the mantle lithosphere represented by the Simcoe xenoliths. Trace element compositions of the clinopyroxenes, and the presence of high alkali glasses in the xenoliths, are consistent with the metasomatic agent derived from the hybridized hanging wall being alkali-rich, and possibly similar to potassic-rich lavas found in arc and back-arc settings. These data therefore demonstrate the importance of the hybridized hanging wall mantle above slabs as a source for melts which can be metasomatic agents in the upper mantle, and as a site for storage of material derived from the slab for periods of at least tens of million years.     

长江中下游中生代安山质火山岩记录的新元古代大洋板片-地幔相互作用

大陆弧安山岩的形成是大洋板片向大陆边缘之下俯冲的结果,但是在具体形成机制上存在很大争议.针对这个问题,对长江中下游地区中生代安山质火山岩及其伴生的玄武质和英安质火山岩进行了系统的岩石地球化学研究,结果对大陆弧安山质火成岩的成因提出了新的机制.分析表明,这些岩石形成于早白垩世,它们不仅表现出典型的岛弧型微量元素分布特征,而且具有高度富集的Sr-Nd-Hf同位素和高的放射成因Pb以及高的氧同位素组成.通过全岩和矿物地球化学成分变化检查发现,地壳混染和岩浆混合作用对其成分的富集特征贡献有限,而其岩浆源区含有丰富的俯冲地壳衍生物质才是其成分富集的根本原因.虽然这些火山岩的喷发年龄为中生代,但是其岩浆源区形成于新元古代早期的华夏洋壳俯冲对扬子克拉通边缘之下地幔楔的交代作用.大陆弧安山岩地幔源区中含有大量俯冲洋壳沉积物部分熔融产生的含水熔体,显著区别于大洋弧玄武岩的地幔源区,其中只含有少量俯冲洋壳来源的富水溶液和含水熔体.正是这些含水熔体交代上覆地幔楔橄榄岩,形成了不同程度富集的超镁铁质-镁铁质地幔源区.在早白垩纪时期,古太平洋俯冲过程的远弧后拉张导致中国东部岩石圈发生部分熔融,其中超镁铁质地幔源区熔融形成玄武质火山岩,镁铁质地幔源区则熔融形成安山质火山岩.因此,大陆弧安山岩成因与大洋弧玄武岩一样,可分为源区形成和源区熔融两个阶段,其中第一阶段对应于俯冲带壳幔相互作用.      

Magmatic evolution of Late Cenozoic volcanic rocks of the Lau Ridge,Fiji

Three main groups of lavas are exposed on islands of the Lau Ridge: the Lau Volcanic Group (LVG), 14.0–5.4 Ma, are predominantly andesite; Korobasaga Volcanic Group (KVG), 4.4–2.4 Ma, are predominantly basalt and Mago Volcanic Group (MVG), 2.0–0.3 Ma, are basalt-hawaiite. LVG and KVG lavas are mostly medium-K tholeiitic rocks with high LILE/HFSE ratios characteristic of islands ares, while MVG lavas are ne-normative alkalic rocks with high LILE and HFSE, characteristic of ocean island basalts. LVG lavas have high ?_Nd (+8.0–+8.4) and low ⁸⁷Sr/⁸⁶Sr (0.70273–0.70349) similar to N-MORB, whereas KVG lavas have slightly more radiogenic values (?_Nd=+7.5?+8.4; ⁸⁷Sr/⁸⁶Sr=0.70323-0.70397). MVG lavas form an isotopically distinct group having lower ?_Nd (+4.6–+4.9) and (⁸⁷Sr/⁸⁶Sr ranging from 0.70347–0.70375). LVG lavas were erupted in a primary oceanic island arc (Vitiaz arc) during the Miocene. Basaltic lavas were derived by approximately 19% partial melting of mantle wedge peridotite with only minor subduction component. Andesites and dacites were produced by low-pressure plagioclase-pyroxene-titanomagnetite dominated crystal fractionation. KVG lavas were erupted during the period immediately prior to or during the initial stages of rifting in the Lau Basin, and, like LVG lavas, show significant chemical differences at the northern and southern ends of the Lau Ridge. Lavas at the northern end (type (ii)) appear to be derived from a more depleted source than LVG but with a greater amount of subduction component. Those at the southern end (type (i)) probably came from a slightly more enriched source with less subduction component. MVG basalts and hawaiites were derived from an enriched mantle with little or no subduction input. The hawaiites (type (i)) could not have been derived from the basalts (type (ii)), and the two magma types must have come from different sources, indicating mantle heterogeneity. The lack of subduction influence indicates the MVG lavas are tectonically unrelated to the present-day Tonga arc, and the lack of depletion indicators suggests they have tapped a different (new?) part of the mantle wedge. This may reflect introduction of sub-Pacific mantle through the present Tonga-Lau subduction system.     

贺兰山汝箕沟玄武岩地球化学特征及其地质意义

贺兰山汝箕沟地区上三叠统延长组顶部发育一套基性火山岩,为我们探讨贺兰山地区晚三叠世的构造属性提供了重要依据。该套火山岩为一套拉斑玄武岩,主量元素以相对富Na₂O （1.29%～3.66%）、贫K₂O （<1%）和低Mg^# （43%～58%）为特征。稀土元素总含量较低（65.13×10^-6～94.52×10^-6）,（La/Yb）_N = 3.46～4.71,为轻稀土富集型。富集Cs、Rb、Ba等大离子亲石元素和高场强元素,结合构造环境判别图解,该套火山岩形成于陆内裂谷环境。岩浆喷溢时间晚于盆地裂陷沉积时间,具被动裂谷性质。综合分析表明,汝箕沟玄武岩岩浆是拉张作用下岩石圈地幔尖晶石二辉橄榄岩与石榴石二辉橄榄岩过渡区域部分熔融的产物,并经历了一定程度的橄榄岩、单斜辉石的结晶分异,表明晚三叠世—早侏罗世阿拉善地块与东部华北板块之间曾经历过一次伸展裂解事件。     

The geochemical variations of mid-Cretaceous lavas across western Shandong Province, China and their tectonic implications

Major and trace element as well as Sr–Nd isotopic compositions of mid-Cretaceous lavas across western Shandong Province, China have been studied. These lavas can be generally divided into southern Shandong group (including Pingyi and Mengyin) and northern Shandong group (including Laiwu and Zouping) based on their geochemistry. The southern group lavas are characterized by extreme enrichment in LREE, large ion lithophile elements (LILE), and depletion in HFSE along with EMII-like Sr–Nd isotopic compositions, suggesting that the crustal involvements play a significant role in their petrogenesis. Comparing studies with Fangcheng basalts reveal that the Triassic continent–continent collision between the Yangtze craton (YC) and the North China craton (NCC), and subsequent extensive modification of the sub-continental lithospheric mantle (SCLM) beneath the south part of the NCC by silicic melts released from the subducted Yangtze lower crust, formed an enriched lithospheric mantle which was the source of the southern Shandong group lavas. In contrast, the northern Shandong group lavas are mildly enriched in LREE and LILE relative to those of the southern group lavas. The isotope compositions are also distinctive in that the Sr isotopic ratios are very low. Available geochemical evidence and comparing studies with spatially closed related mafic intrusions suggest that the SCLM feeding the northern group lavas seems to be linked to carbonatitic metasomatism and changed modal proportion of phlogopite and clinopyroxene in the mantle rather than subduction-related modifications. The contrasting geochemical characters of the mid-Cretaceous lavas across western Shangdong suggest that the SCLM of the NCC is spatially heterogeneous in Mesozoic.     

南菲律宾地区类埃达克岩和富铌玄武质熔岩的成因

埃达克岩（adakite)最初 是指由消减板片玄武岩物质熔融形成的富硅、富钠、高Sr/Y和La/Yb比值的弧火山熔岩。它通常产在会聚带，这个部位的年轻的、因而仍然是热的大洋板片正在发生俯冲消减。富铌的岛弦玄武央进则是吕等到高碱的镁铁质熔岩，它们相对于正常的岛弦玄武岩含有较多的高场强元素（HFSE）。这些玄武岩通常与埃达克央共生， 这一组合是直被用于论证他们的高HFSE含量是因为他们的地幔源区受到板片来源的熔体的交代。先前的区域研究结果表明，南菲律宾是埃达克岩和富铌岛孤玄武岩的一个典型产地。然而最近的详细研究显示，尽管该地区的一些岛弧火山岩是类埃达克岩的，但是它们很可能是来自地幔楔的母岩浆的分异作用的产物，而这里的地幔楔主要是受沉积来源的成分交代的，此外，菲律宾南部最典型的富铌熔岩中HFSE的富集，也很有可能是起因于似乎是西太平洋边缘特有的富集地幔组分的熔融。这些结果提出了如下问题：南菲律宾是否存在真正的板片来源的熔体？这里的富铌岛弧 熔岩是否起因于地幔楔被这种熔体交代？     

内蒙古北山地区芨芨台子-小黄山蛇绿岩构造属性及与成矿关系: 来自阿民乌素地幔橄榄岩印证

阿民乌素地幔橄榄岩属芨芨台子-小黄山蛇绿岩带一部分,该构造带南北两侧地质体无明显差异,不具分界断裂的构造特征。本文对阿民乌素地幔橄榄岩与月牙山地幔橄榄岩进行岩石化学、地球化学对比分析,为芨芨台子-小黄山蛇绿岩构造属性提供新依据,并对阿民乌素蛇绿岩成矿潜力进行分析研究。笔者所在团队在地幔橄榄岩上部的辉长岩中获得LA-ICP-MS锆石U-Pb同位素年龄值为462.5±3.2 Ma,属中奥陶世。其上发育奥陶纪-志留纪公婆泉组岛弧拉斑玄武岩。该期地幔橄榄岩轻重稀土之比LR/HR＝1.63~3.68, (La/Sm)N＝1.70~6.92,(Gd/Yb)N＝0.36~0.52,表明岩石轻稀土略富集,稀土配分曲线呈不规则“U”型,估算其为原始地幔橄榄岩经过10%~20%部分熔融的残留物。原始地幔标准化蛛网图富集高场强元素U、Zr、Hf、Yb和大离子亲石元素Rb、Sr,亏损高场强元素Nb、Ti和大离子亲石元素Ba。与月牙山地幔橄榄岩标准化蛛网图对比,最大区别在于阿民乌素地幔橄榄岩明显亏损高场强元素Ti。初步研究认为阿民乌素地幔橄榄岩属SSZ型、高压型蛇绿岩,是岛弧裂谷的产物。该橄榄岩具有形成大型铬铁矿的成矿构造背景,是寻找蛇绿岩型铬铁矿的有利部位。     

Arc‐nascent back‐arc signature in metabasalts from the Neoarchaean Jonnagiri greenstone terrane,Eastern Dharwar Craton,India

The Neoarchaean Jonnagiri greenstone terrane (JGT) is located at the centre of the arcuate Hutti–Jonnagiri–Kadiri–Kolar composite greenstone belt in the eastern Dharwar Craton. High MgO (MgO = ~14 wt.%; Nb = 0.2 ppm), low Nb (LNB) (MgO = 7.8–12 wt.%; Nb = 0.1–5.1 ppm) and high Nb basalts (HNB) (MgO = 5.6–10.1 wt.%; Nb = 9.0–10.6 ppm) metamorphosed to lower amphibolite facies are identified based on their geochemical compositions. These metabasalts exhibit depleted HFSE (Nb–Ta, Zr–Hf), pronounced LREE and LILE enrichments suggesting contribution from subduction‐related components during their genesis. Th and U enrichment over Nb–Ta indicates influx of fluids dehydrated from subducted oceanic lithosphere. The high MgO basalts with higher Mg# (51) than that of the associated LNB and HNB (Mg# = 34–47) represent early fractionated melts of subduction‐modified mantle peridotite. The LNB were produced by partial melting of mantle wedge metasomatized by slab‐dehydrated fluids, whereas the HNB represents melts of subducted oceanic crust and hybridized mantle wedge. Lower Dy/Yb and variable La/Yb ratios suggest their generation at shallower depth within spinel peridotite stability field. The low Ce–Yb trend of these metabasalts reflects intraoceanic type subduction which straddles the fields of arc and back‐arc basin basalts, resembling the Mariana‐type arc basalts. The Jonnagiri metabasalts were derived in a paired arc‐back‐arc setting marked by nascent back‐arc rift system that developed in the proximity of an intraoceanic arc. Copyright © 2014 John Wiley & Sons, Ltd.     

富铌玄武岩：板片熔体交代的地幔楔橄榄岩部分熔融产物

富铌玄武岩是一类具有特殊地球化学特征的岛弧玄武岩。与正常岛弧玄武岩相比，它具有硅饱和并富钠的特征；同时具有相对高的Nb（一般>7×10-6）、TiO2（1%～2%）和P含量，以及低的LILE/HFSE和HREE/HFSE比值，并富集高场强元素；它的原始地幔标准化微量元素图显示了弱的Nb、Ta负异常（有时出现弱的正异常），原始地幔标准化La/Nb比值小于2（但很少小于0.7），它是由受埃达克质熔体交代过的地幔橄榄岩部分熔融形成的。由于富铌玄武岩与埃达克岩是大洋板片俯冲作用的直接产物，因此，通过对该岩石组合及与俯冲作用有关的流体和熔体的研究，不仅可以查明洋壳俯冲作用过程中的岩浆活动特征，还可以阐明洋壳俯冲及壳幔相互作用，具十分重要的地质意义。     

Magmatic processes and mantle heterogeneity beneath the slow-spreading northern Kolbeinsey Ridge segment,North Atlantic

We present new data on mineralogical, major and trace element compositions of lavas from the northernmost segment of the Kolbeinsey Ridge (North Kolbeinsey Ridge, NKR). The incompatible element enriched North Kolbeinsey basalts lie on a crystal fractionation trend which differs from that of the other Kolbeinsey segments, most likely due to higher water contents (~0.2%) in the NKR basalts. The most evolved NKR magmas erupt close to the Jan Mayen Fracture Zone, implying increased cooling and fractionation of the ascending magmas. Mainly incompatible element-enriched basalts, as well as some slightly depleted lavas, erupt on the NKR. They show evidence for mixing between different mantle sources and magma mixing. North Kolbeinsey Ridge magmas probably formed by similar degrees of melting to other Kolbeinsey basalts, implying that no lateral variation in mantle potential temperature occurs on the spreading axis north of the Iceland plume and that the Jan Mayen Fracture Zone does not have a cooling effect on the mantle. Residual garnet from deep melting in garnet peridotite or from enriched garnet pyroxenite veins does not play a role. The incompatible element-enriched source has high Ba/La and Nb/Zr, but must be depleted in iron. The iron-depleted mantle is less dense than surrounding mantle and leads to the formation of the North Kolbeinsey segment and its shallow bathymetry. The enriched NKR source formed from a relatively refractory mantle, enriched by a small degree melt rather than by recycling of enriched basaltic crust. The depleted mantle source resembles the mantle of the Middle Kolbeinsey segment with a depletion in incompatible elements, but a fertile major element composition.     

Petrogenesis of the Neogene volcanic units in the NE–SW-trending basins in western Anatolia,Turkey

The western Anatolian volcanic province formed during Eocene to Recent times is one of the major volcanic belts in the Aegean–western Anatolian region. We present new chemical (whole-rock major and trace elements, and Sr, Nd, Pb and O isotopes) and new Ar/Ar age data from the Miocene volcanic rocks in the NE–SW-trending Neogene basins that formed on the northern part of the Menderes Massif during its exhumation as a core complex. The early-middle Miocene volcanic rocks are classified as high-K calc-alkaline (HKVR), shoshonitic (SHVR) and ultrapotassic (UKVR), with the Late Miocene basalts being transitional between the early-middle Miocene volcanics and the Na-alkaline Quaternary Kula volcanics (QKV). The early-middle Miocene volcanic rocks are strongly enriched in large ion lithophile elements (LILE), have high ⁸⁷Sr/⁸⁶Sr_(i) (0.70631–0.71001), low ¹⁴³Nd/¹⁴⁴Nd_(i) (0.512145–0.512488) and high Pb isotope ratios (²⁰⁶Pb/²⁰⁴Pb = 18.838–19.148; ²⁰⁷Pb/²⁰⁴Pb = 15.672–15.725; ²⁰⁸Pb/²⁰⁴Pb = 38.904–39.172). The high field strength element (HFSE) ratios of the most primitive early-middle Miocene volcanic rocks indicate that they were derived from a mantle source with a primitive mantle (PM)-like composition. The HFSE ratios of the late Miocene basalts and QKV, on the other hand, indicate an OIB-like mantle origin—a hypothesis that is supported by their trace element patterns and isotopic compositions. The HFSE ratios of the early-middle Miocene volcanic rocks also indicate that their mantle source was distinct from those of the Eocene volcanic rocks located further north, and of the other volcanic provinces in the region. The mantle source of the SHVR and UKVR was influenced by (1) trace element and isotopic enrichment by subduction-related metasomatic events and (2) trace element enrichment by “multi-stage melting and melt percolation” processes in the lithospheric mantle. The contemporaneous SHVR and UKVR show little effect of upper crustal contamination. Trace element ratios of the HKVR indicate that they were derived mainly from lower continental crustal melts which then mixed with mantle-derived lavas (~20–40%). The HKVR then underwent differentiation from andesites to rhyolites via nearly pure fractional crystallization processes in the upper crust, such that have undergone a two-stage petrogenetic evolution.     

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

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