雷琼地区晚新生代玄武岩地球化学：EM2成分来源及大陆岩石圈地幔的贡献

对雷琼地区21个晚新生代玄武岩样品的主量、微量元素和Sr、Nd、Pb同位素分别用湿化学法、ICP-MS和MC-ICPMS进行了测定.这些玄武岩主要为石英拉斑玄武岩,其次为橄榄拉斑玄武岩和碱性玄武岩.大多数样品的微量元素和同位素成分与洋岛玄武岩(OIBs)相似,而且随着SiO_2不饱和度增加,不相容元素含量也增加.除R4-1可能受到地壳混染外,其他样品相对均一的Nd同位素(ε_(Nd)=2.5-6.0)以及变化明显但范围有限的Sr同位素(0.703106～0.704481),可能继承了地幔源区的特征.~(87)Sr/~(86)Sr与~(206)Pb/~(204)Pb的正相关和~(143)Nd/~(144)Nd与~(206)Pb/~(204)Pb的负相关特征暗示DM(软流圈地幔)与EM2(岩石圈地幔)的混合.地幔捕虏体的同位素特征暗示EM2成分不可能存在于尖晶石橄榄岩地幔,而La/Yb和Sm/Yb系统表明岩浆由石榴石橄榄岩部分熔融产生,这意味着EM2成分可能存在于石榴石橄榄岩地幔.雷琼地区玄武岩的地球化学变化可以用软流圈地幔为主的熔体加入不同比例石榴石橄榄岩地幔不同程度熔融产生的熔体来解释:碱性玄武岩和橄榄拉斑玄武岩是软流圈熔体与石榴石橄榄岩地幔较低程度(7%～9%)熔融体混合,而石英拉斑玄武岩是软流圈熔体与石榴石橄榄岩地幔较高程度(10%～20%)熔融体的混合.     

Os, Nd, and Sr isotopic and chemical compositions of ultramafic xenoliths from Kurose, SW Japan: Implications for contribution of slab-derived material to wedge mantle

We examined seven ultramafic xenoliths from 1~3 Ma alkali olivine basalt reefs near the Eurasian continent and one sample of the host alkali basalt to identify the mantle wedge material and to constrain the origin and evolution of mantle beneath SW Japan. Six xenoliths are from Kurose and one xenolith is from Takashima, northern part of the Kyushu islands, SW Japan. The Sr and Nd isotopic ratios vary from 0.70416 to 0.70773 and from 0.51228 to 0.51283, respectively. The Kurose and Takashima xenoliths have higher Sr isotopic ratios and lower Nd isotopic ratios than those of the peridotite xenoliths from the other arc settings such as Simcoe and NE Japan.

The Kurose xenoliths have less radiogenic Os isotopic ratios (¹⁸⁷Os/¹⁸⁸Os = 0.123–0.129) than the primitive upper mantle (PUM) estimate and limited variation compared to the other arc xenoliths. Their Os isotope compositions are rather similar to the ultramafic xenoliths from NE and east China. In addition, the samples of the Kurose and Takashima xenoliths plot along a mixing line between ultramafic xenoliths from SE and NE China and a slab component in Sr–Nd–Os isotopic space. Our results suggest that fragments of continental lithospheric mantle from the China craton may exist beneath Kurose and Takashima after the Sea of Japan expansion when the Japanese islands were rifted away from the Eurasian continent during Miocene. Later magmatism due to subduction of the Philippine Sea Plate beneath the SW Japan arc around 15 Ma ago may have introduced fluids or melts derived from slab component, interpreted to be oceanic sediments rather than altered oceanic crust, that possibly modified the original composition of the lithospheric mantle sampled by the peridotite xenoliths from Kurose and Takashima.     

Sr isotopes in peridotite xenoliths and their basaltic host rocks from the northern Hessian Depression (NW Germany)

⁸⁷Sr/⁸⁶Sr ratios of alkali olivine basalts, nepheline basanites and olivine nephelinites of Miocene age from the northern Hessian Depression vary between 0.7032 and 0.7036. Tholeiitic rocks from this area, which are possibly affected by crustal contamination, have more radiogenic Sr (0.7035 to 0.7042). Peridotite xenoliths with coarse protogranular (10 samples) and with porphyroclastic textures (2 samples) contain K- and Na-rich glasses which are products of reaction of metasomatic fluids with depleted peridotite. The Sr abundance in xenoliths is related to the amount of glass (and phlogopite).Sr ranges from 11 ppm to 147 ppm and ⁸⁷Sr/⁸⁶Sr ratios from 0.7033 to 0.7039. The isotopic ratios are neither correlated with Sr concentrations nor with Rb/Sr ratios. ⁸⁷Sr/ ⁸⁶Sr ratios of etched clinopyroxenes range from 0.7028 to 0.7040. In some xenoliths, clinopyroxenes differ from the whole rock samples significantly in their isotopic composition.If almost all of the pre-metasomatic Sr was located in the clinopyroxenes, the metasomatically introduced Sr ranges from 35 to 80% of the whole rock Sr. The calculated isotopic composition ranges from 0.7033 to 0.7040 for the majority of the xenoliths. For two pyroxenes which are not in isotopic equilibrium with the whole rock, the age of the metasomatic event could be estimated on the base of diffusion of Sr in clinopyroxene. Even assuming a diffusion coefficient as low as 10^–15 cm²s^–1 the time between the metasomatic alteration and the eruption of the basaltic host magma must be shorter than 1 Ma.The ⁸⁷Sr/⁸⁶Sr ratios of the basalts are interpreted as products of mixtures of a depleted component ( 0.7028) and metasomatic fluids (0.7035–0.7053) in their source peridotite.     

Emplacement age and isotope geochemistry of Sung Valley alkaline–carbonatite complex, Shillong Plateau, northeastern India: implications for primary carbonate melt and genesis of the associated silicate rocks

The early Cretaceous (Albian–Aptian) Sung Valley ultramafic–alkaline–carbonatite complex is one of several alkaline intrusions that occur in the Shillong Plateau, India. This complex comprises calcite carbonatite and closely associated ultramafic (serpentinized peridotite, pyroxenite and melilitolite) and alkaline rocks (ijolite and nepheline syenite). Field relationship and geochemical characteristics of these rocks do not support a genetic link between carbonatite and associated silicate rocks. There is geochemical evidence that pyroxenite, melilitolite and ijolite of the complex are genetically related. Stable (C and O) and radiogenic (Nd and Sr) isotope data clearly indicate a mantle origin for the carbonatite samples. The carbonatite Nd (+0.7 to +1.8) and Sr (+4.7 to +7.0) compositions overlap the field for Kerguelen ocean island basalts. One sample of ijolite has Nd and Sr isotopic compositions that also plot within the field for Kerguelen ocean island basalts, whereas the other silicate–carbonatite samples indicate involvement with an enriched component. These geochemical and isotopic data indicate that the rocks of the Sung Valley complex were derived from and interacted with an isotopically heterogeneous subcontinental mantle and is consistent with interaction of a mantle plume (e.g. Kerguelen plume) with lithosphere. A U–Pb perovskite age of 115.1±5.1 Ma obtained for a sample of Sung Valley ijolite also supports a temporal link to the Kerguelen plume. The observed geochemical characteristics of the carbonatite rocks indicate derivation by low-degree partial melting (0.1%) of carbonated mantle peridotite. This melt, containing a substantial amount of alkali elements, interacted with peridotite to form metasomatic clinopyroxene and olivine. This process could progressively metasomatize lherzolite to form alkaline wehrlite.     

Iron isotope variations in spinel peridotite xenoliths from North China Craton: implications for mantle metasomatism

Iron isotopes, together with mineral elemental compositions of spinel peridotite xenoliths and clinopyroxenites from Hannuoba and Hebi Cenozoic alkaline basalts, were analyzed to investigate iron isotopic features of the lithospheric mantle beneath the North China Craton. The results show that the Hannuoba spinel peridotite xenoliths have small but distinguishable Fe isotopic variations. Overall variations in δ⁵⁷Fe are in a range of ?0.25 to 0.14‰ for olivine, ?0.17 to 0.17‰ for orthopyroxene, ?0.21 to 0.27‰ for clinopyroxene, and ?0.16 to 0.26‰ for spinel, respectively. Clinopyroxene has the heaviest iron isotopic ratio and olivine the lightest within individual sample. No clear linear relationships between the mineral pairs on “δ-δ” plot suggest that iron isotopes of mineral separates analyzed have been affected largely by some open system processes. The broadly negative correlations between mineral iron isotopes and metasomatic indexes such as spinel Cr#, (La/Yb)_N ratios of clinopyroxenes suggest that iron isotopic variations in different minerals and peridotites were probably produced by mantle metasomatism. The Hebi phlogopite-bearing lherzolite, which is significantly modified by metasomatic events, appears to be much heavier isotopically than clinopyroxene-poor lherzolite. This study further confirms previous conclusions that the lithospheric mantle has distinguishable and heterogeneous iron isotopic variations at the xenoliths scale. Mantle metasomatism is the most likely cause for the iron isotope variations in mantle peridotites.     

The composition and formation of Miocene tholeiites in the Central European Cenozoic plume volcanism (CECV)

Tholeiites accompanying a majority of alkali basalts are restricted to the highly productive central part of the CECV plume activity in Vogelsberg and Hessian Depression. They mainly occur as quartz tholeiites which according to experiments of partial melting and material balances are products of olivine tholeiitic primary melts. The differentiation from olivine to quartz tholeiitic melts took place in lower crustal magma chambers where olivine tholeiitic melt intruded due to a density comparable with that of the country rocks. The fractionation due to separation of olivine and some clinopyroxene caused contamination of tholeiite magmas by tonalitic partial melts from the wall rocks of the magma chambers. The latter process is indicated by relatively high Rb, K and Pb and low Nb concentrations and by Nd, Sr and Pb isotopes. Contaminating crustal melts, which roughly attained a proportion of 10%, contained very low ¹⁴³Nd/¹⁴⁴Nd ratios from a Nd/Sm fractionation as old as 2.6 Ga. This is the first evidence from mafic rocks of this high age in the lower crust beneath Central Europe. Modelling with incompatible elements allows to recognize olivine tholeiites as products of about 1% partial melting of plume rocks consisting of 35% primitive and 65% depleted mantle materials. The production of tholeiites other than alkali basalts is restricted to the highest plume activity and the largest fraction of MORB type source rocks. Received: 10 December 1999 / Accepted: 23 June 2000     

Petrological, geochemical and isotopic characteristics of the lithospheric mantle beneath Sardinia (Italy) as indicated by ultramafic xenoliths enclosed in alkaline lavas

Mantle xenoliths hosted in Miocene-Quaternary mafic alkaline volcanic rocks from Sardinia have been investigated with electron microprobe, laser ablation microprobe-inductively coupled plasma-mass spectrometry and thermal ionization mass spectrometry techniques. The xenoliths are anhydrous clinopyroxene-poor lherzolites and harzburgites, plus very rare websterites and olivine-websterites. Glassy pods having thin subhedral to euhedral microlites of olivine, clinopyroxene and spinel have been found in harzburgites and websterites. Clinopyroxene shows trace element variability, with values of (La/Yb)_N ranging from sub-chondritic (0.01) to supra-chondritic (8.6). The Sr–Nd isotopic ratios of the clinopyroxenes fall mostly in the field of the European lithospheric mantle xenoliths (⁸⁷Sr/⁸⁶Sr from 0.70385 to 0.70568 and ¹⁴³Nd/¹⁴⁴Nd ranging from 0.512557 to 0.512953). The geochemical characteristics of the Sardinian xenoliths testify to the variable degrees of earlier partial melt extraction, followed by metasomatic modification by alkaline melts or fluids. Websterites are considered to represent small lenses or veins of cumulitic (i.e. magmatic) origin within the mantle peridotite.     

Erratum to: Iron isotope variations in spinel peridotite xenoliths from North China Craton: implications for mantle metasomatism

Iron isotopes, together with mineral elemental compositions of spinel peridotite xenoliths and clinopyroxenites from Hannuoba and Hebi Cenozoic alkaline basalts, were analyzed to investigate iron isotopic features of the lithospheric mantle beneath the North China Craton. The results show that the Hannuoba spinel peridotite xenoliths have small but distinguishable Fe isotopic variations. Overall variations in δ⁵⁷Fe are in a range of −0.25 to 0.14‰ for olivine, −0.17 to 0.17‰ for orthopyroxene, −0.21 to 0.27‰ for clinopyroxene, and −0.16 to 0.26‰ for spinel, respectively. Clinopyroxene has the heaviest iron isotopic ratio and olivine the lightest within individual sample. No clear linear relationships between the mineral pairs on “δ-δ” plot suggest that iron isotopes of mineral separates analyzed have been affected largely by some open system processes. The broadly negative correlations between mineral iron isotopes and metasomatic indexes such as spinel Cr#, (La/Yb)_N ratios of clinopyroxenes suggest that iron isotopic variations in different minerals and peridotites were probably produced by mantle metasomatism. The Hebi phlogopite-bearing lherzolite, which is significantly modified by metasomatic events, appears to be much heavier isotopically than clinopyroxene-poor lherzolite. This study further confirms previous conclusions that the lithospheric mantle has distinguishable and heterogeneous iron isotopic variations at the xenoliths scale. Mantle metasomatism is the most likely cause for the iron isotope variations in mantle peridotites.     

Quaternary Tholeiitic to Alkaline Volcanism in the Karasu Valley,Dead Sea Rift Zone,Southeast Turkey: Sr-Nd-Pb-O Isotopic and Trace-Element Approaches to Crust-Mantle Interaction

Rare-earth-element, radiogenic and oxygen isotope, and mineral chemical data are presented for tholeiitic and alkaline Quaternary volcanism from Karasu Valley (Hatay, southeastern Turkey). Karasu Valley is the northern segment of the Dead Sea transform fault and is filled with flood-basalt type volcanics of Quaternary age. This valley is an active fault zone that is known as “Karasu fault,” extending in a NE-SW direction. The Karasu Valley basaltic volcanics (KVBV) are subaphyric to porphyritic, with variable amounts of olivine, clinopyroxene, and plagioclase phenocrysts. Alkali basalts are generally characterized by high contents of olivine, clinopyroxene, and plagioclase phenocrysts. Their groundmass contains olivine, clinopyroxene, plagioclase, and Fe-Ti oxides. Tholeiitic basalts are subaphyric to porphyritic (high contents of olivine, clinopyroxene, and plagioclase). Their groundmass is similar to that of alkali basalts. The range of olivine phenocryst and microlite compositions for all analyzed samples is Fo₈₁ to Fo₄₃. Plagioclase compositions in both tholeiitic and alkali basalts range from andesine, An₃₈ to bytownite, An₇₂. Clinopyroxene compositions range from diopside to calcic augite. Most of the olivine, plagioclase, and clinopyroxene phenocrysts are normally zoned and/or unzoned. Fe-Ti oxides in both series are titanomagnetite and ilmenite.

Based on normative and geochemical data, the Karasu Valley basaltic volcanics are mostly olivine and quartz-tholeiites, and relatively lesser amount of alkali olivine-basalts. KVBV have low K₂O/Na₂O ratios, typically between 0.25 and 0.45. Olivine- and quartz-tholeiites are older than alkali olivine-basalts. Olivine tholeiites have Zr/Nb and Y/Nb ratios similar to alkaline rocks, but their Ba/Nb, Ba/La, and La/Nb ratios are slightly higher than alkali olivine-basalts. In contrast, quartz-tholeiites have the highest Ba/Nb, Ba/La, Zr/Nb, and Y/Nb and the lowest Nb/La ratios among the KVBV. Alkali basalts have ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios ranging from 0.703353 to 0.704410 and 0.512860 to 0.512910, respectively. In contrast, quartz-tholeiites have higher ⁸⁷Sr/⁸⁶Sr and lower ¹⁴³Nd/¹⁴⁴Nd ratios, which vary from 0.704410 to 0.705490 and 0.512628 to 0.512640, respectively. Olivine tholeiites have intermediate isotopic compositions ranging from 0.703490 to 0.704780 and 0.512699 to 0.512780, respectively. ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb isotopic ratios of KVBV range from 18.817 to 19.325, 15.640 to 15.718, and 39.054 to 39.223, respectively. The range of O isotope values is between +5.84 and +7.97‰. The higher O and Sr isotopes in olivine- and quartz-tholeiites relative to alkali olivine-basalts can be explained by contamination of magmas by crustal materials.

The KVBV have intraplate chemistry similar to that of other tholeiitic and alkaline basalts in other within-plate environments, and isotopes range from isotopically depleted mantle to enriched isotope compositions similar to some enriched ocean islands. Trace-element and isotope data indicate that the KVBV are derived from a common OIB-like asthenospheric mantle source, but they have experienced different degrees of crustal contamination during their ascent to the surface, contemporaneous with little fractional crystallization. Although quartz-tholeiites display significant effects of crustal contamination, alkali olivine-basalts appear to have negligible or no crustal contamination in their geesis.     

Sr and Nd isotope composition of deformed peridotite xenoliths from Udachnaya kimberlite pipe

New results of Rb–Sr and Sm–Nd isotope analyses have been obtained on samples of deformed peridotite xenoliths collected from the Udachnaya kimberlite pipe (Yakutia). The data obtained imply two main stages of metasomatic alteration of the lithospheric mantle base matter in the central part of the Siberian Craton. Elevated ratios of Sr isotopes may be considered as evidence of an ancient stage of metasomatic enrichment by a carbonatite melt. The acquired Nd isotope composition together with the geochemistry of the deformed peridotite xenoliths suggests that the second stage of metasomatic alteration took place shortly before formation of the kimberlite melt. The metasomatic agent of this stage had a silicate character and arrived from an asthenosphere source, common for the normal OIB type (PREMA) and the Group-I kimberlite.

     

Petrogenesis of plio-quaternary intra-plate continental alkaline lavas from the İskenderun Gulf (Southern Turkey): Evidence for metasomatized lithospheric mantle

The Quaternary alkaline volcanic field of Southern Turkey is characterized by intra-continental plate-type magmatic products, exposed to the north of the ?skenderun Gulf along a NE-SW trending East Anatolian Fault, to the west of its intersection with the N–S trending Dead Sea Fault zone. The ?skenderun Gulf alkaline rocks are mostly silica-undersaturated with normative nepheline and olivine and are mostly classified as basanites and alkaline basalts with their low-silica contents ranging between 43 and 48?wt.% SiO₂. They display Ocean Island Basalt (OIB)–type trace element patterns characterized by enrichments in large-ion-lithophile elements (LILE) and light rare earth element (LREE), and have (La/Yb)_N?=?8.8–17.7 and (Hf/Sm)_N?=?0.9–1.6 similar to those of basaltic rocks found in intraplate suites. The basanitic rocks have limited variations Sr-Nd isotopic ratios (⁸⁷Sr/⁸⁶Sr?=?0.70307–0.70324, ¹⁴³Nd/¹⁴⁴Nd?=?0.512918–0.521947), whereas the alkali basalts display more evolved Sr-Nd isotopic ratios (⁸⁷Sr/⁸⁶Sr?=?0.70346-0.70365, ¹⁴³Nd/¹⁴⁴Nd?=?0.512887–0.521896). The ?skenderun Gulf alkaline rocks also display limited Pb isotopic variations with ²⁰⁶Pb/²⁰⁴Pb?=?18.75–19.09 ²⁰⁷Pb/²⁰⁴Pb?=?15.61–15.66 and²⁰⁸Pb/²⁰⁴Pb?=?38.65–39.02, indicating that they originated from an enriched lithospheric mantle source. Calculated fractionation vectors indicate that clinopyroxene and olivine are the main fractionating mineral phases. Similarly, based on Sr-Nd isotopic ratios, the assimilation and fractional crystallization (AFC) modeling shows that the alkali basalts were affected by AFC processes (r?=?0.2) and were slightly contaminated by the upper crustal material.The high TiO₂ contents, enrichments in Ba and Nb, and depletions in Rb can likely be explained by the existence of amphibole in the mantle source, which might, in turn, indicate that the source mantle has been affected by metasomatic processes. The modeling based on relative abundances of trace elements suggests involvement of amphibole-bearing peridotite as the source material. ?skenderun Gulf alkaline rocks can thus be interpreted as the products of variable extent of mixing between melts from both amphibole-bearing peridotite and dry peridotite.     

Magmatic modification of the uppermost mantle beneath the Basin and Range to Colorado Plateau Transition Zone; Evidence from xenoliths, Wikieup, Arizona

Upper mantle xenoliths from Wikieup, AZ, provide abundant evidence for magmatic modification of the uppermost mantle beneath the Transition Zone between the Colorado Plateau and the southern Basin and Range province. Upper mantle lithologies in this xenolith suite are represented by spinel peridotite, wehrlite, plagioclase peridotite, and Al-augite group pyroxenites. Isotopic data for these xenoliths yield relatively uniform values and suggest a common petrogenesis. Al-augite-bearing gabbro and pyroxenite xenoliths from this locality are interpreted to have formed by crystal fractionation processes from parent alkali basalts similar to the Wikieup host basalt. Mineral and whole rock compositions show consistent trends of increasing incompatible element contents (Fe, Al, Ca, Na, K, LIL, and LREE), and decreasing compatible element contents (Mg, Cr, Ni) from spinel peridotite to wehrlite to plagioclase peridotite to the host basalt composition. These compositional trends are interpreted as resulting from varying degrees of magma-mantle wall rock interaction as ascending mafic magmas infiltrated upper mantle peridotite. Small degrees of melt infiltration resulted in slightly modified spinel peridotite compositions while moderate degrees metasomatized spinel peridotite to wehrlite, and the highest degrees metasomatized it to plagioclase peridotite. Whole rock compositions and clinopyroxene, plagioclase, and whole rock isotopic data suggest that the infiltrating magmas were the same as those from which the gabbros and pyroxenites crystallized, and that they were alkalic in composition, similar to the Wikieup host alkali olivine basalts. Relatively uniform ¹⁴³Nd/¹⁴⁴Nd for the mineral separates and whole rocks in spite of the significantly wide range in their ¹⁴⁷Sm/¹⁴⁴Nd (0.71–0.23 in clinopyroxene) suggests that the Wikieup xenoliths including gabbro, pyroxenite, peridotite, wehrlite, and plagioclase peridotite, are all relatively young rocks formed or metasomatized by a relatively recent magmatic episode. Received: 21 May 1996 / Accepted: 23 December 1996     

Geochemical Records of Mantle Processes in Mantle Xenoliths from Three Cenozoic Basaltic Volcanoes in Eastern China

Rare earth element (REE) contents, and Sr and Nd isotopic compositions were measured for three suites of mantle xenoliths from the Kuandian, Hannuoba and Huinan volcanoes in the north of the Sino-Korean Platform. From the correlations of Yb contents with Al/Si and Ca/Si ratios, the peridotites are considered to be the residues of partial melting of the primitive mantle. The chondrite-normalized REE compositions are diverse, varying from strongly LREE-depleted to LREE-enriched, with various types of REE patterns. Metasomatic alteration by small-volume silicate melts, of mantle peridotites previously variably depleted due to fractional melting in the spinel peridotite field, can account for the diversity of REE patterns. The Sr/ Ba versus La/Ba correlation indicates that the metasomatic agent was enriched in Ba over Sr and La, suggestive of its volatile-rich signature and an origin by fluid-triggered melting in an ancient subduction zone. The Sr and Nd isotopic compositions of these xenoliths, even from     

The role of mantle-hybridization and crustal contamination in the petrogenesis of lithospheric mantle-derived alkaline rocks: constraints from Os and Hf isotopes

The Rhön area as part of the Central European Volcanic Province (CEVP) hosts an unusual suite of Tertiary 24-Ma old hornblende-bearing alkaline basalts that provide insights into melting and fractionation processes within the lithospheric mantle. These chemically primitive to slightly evolved and isotopically (Sr, Nd, Pb) depleted basalts have slightly lower Hf isotopic compositions than respective other CEVP basalts and Os isotope compositions more radiogenic than commonly observed for continental intraplate alkaline basalts. These highly radiogenic initial ¹⁸⁷Os/¹⁸⁸Os ratios (0.268–0.892) together with their respective Sr–Nd–Pb isotopic compositions are unlikely to result from crustal contamination alone, although a lack of Os data for lower crustal rocks from the area and limited data for CEVP basalts or mantle xenoliths preclude a detailed evaluation. Similarly, melting of the same metasomatized subcontinental lithospheric mantle as inferred for other CEVP basalts alone is also unlikely, based on only moderately radiogenic Os isotope compositions obtained for upper mantle xenoliths from elsewhere in the province. Another explanation for the combined Nd, Sr and Os isotope data is that the lavas gained their highly radiogenic Os isotope composition through a mantle “hybridization”, metasomatism process. This model involves a mafic lithospheric component, such as an intrusion of a sublithospheric primary alkaline melt or a melt derived from subducted oceanic material, sometime in the past into the lithospheric mantle where it metasomatized the ambient mantle. Later at 24 Ma, thermal perturbations during rifting forced the isotopically evolved parts of the mantle together with the peridotitic ambient mantle to melt. This yielded a package of melts with highly correlated Re/Os ratios and radiogenic Os isotope compositions. Subsequent movement through the crust may have further altered the Os isotope composition although this effect is probably minor for the majority of the samples based on radiogenic Nd and unradiogenic Sr isotope composition of the lavas. If the radiogenic Os isotope composition can be explained by a mantle-hybridization and metasomatism model, the isotopic compositions of the hornblende basalts can be satisfied by ca. 5–25% addition of the mafic lithospheric component to an asthenospheric alkaline magma. Although a lack of isotope data for all required endmembers make this model somewhat speculative, the results show that the Re–Os isotope system in continental basalts is able to distinguish between crustal contamination and derivation of continental alkaline lavas from isotopically evolved peridotitic lithosphere that was contaminated by mafic material in the past and later remelted during rifting. The Hf isotopic compositions are slightly less radiogenic than in other alkaline basalts from the province and indicate the derivation of the lavas from low Lu–Hf parts of the lithospheric mantle. The new Os and Hf isotope data constrain a new light of the nature of such metasomatizing agents, at least for these particular rocks, which represent within the particular volcanic complex the first product of the volcanism.     

Sr,Nd and Pb isotopic and REE geochemistry of St. Paul's Rocks: the metamorphic and metasomatic development of an alkali basalt mantle source

Surface samples of peridotites and hornblendite mylonites from St. Paul's Rocks, and dredge samples from the flanks of the massif, have been analyzed for Sr, Nd and Pb isotopic ratios and Rb, Sr, and REE concentrations. This data, coupled with previous K and REE data, are used to develop a self-consistent model for the genesis of these ultramafic rocks. This model involves metasomatism of an ocean island-type mantle about 155 m.y. ago by a strongly light-REE-enriched metasomatic fluid, probably derived from the same mantle. This metasomatism produced light-REE-enriched materials which were isotopically homogeneous on a small scale (100 m), and isotopically heterogeneous on a large (km) scale. The geochemical relationships between the peridotites and the hornblendites were established by metamorphic equilibration on a relatively small scale (<10 m). The average mantle produced by these events is characterized by⁸⁷Sr/⁸⁶Sr=0.7034,¹⁴³Nd/¹⁴⁴Nd=0.51291,²⁰⁶Pb/²⁰⁴Pb=19.33 and 207/204=15.63. An alkali basalt which postdates the mylon-itization of the ultramafic massif has an isotopic character which is identical to the average ultramafic massif; it also lies on the five-dimensional isotopic mantle plane of Zindler et al. (1982). With respect to major elements, trace elements, and Sr, Nd and Pb isotopes, the average ultramafic rock of the St. Paul's massif is an ideal candidate for a mantle source from which alkali basalts can be derived by partial melting; the St. Paul's massif is in fact the first such example of an ultramafic rock which meets all the requirements to be an alkali basalt source.     

Cenozoic alkali basaltic magmas of western Germany and their products of differentiation

Analytical data on major elements and 31 trace elements in olivine nephelinites, nepheline basanites, basanitic alkali olivine basalts and their differentiates (tephrites, hawaiites, mugearites, benmoreites, latites, phonolites and trachytes) from Hegau, Kaiserstuhl, Rhön, Hessian Depression, Vogelsberg, Westerwald, Siebengebirge, E Eifel and Hocheifel are evaluated. They were based on 400 samples with new or unpublished data on about one third of the rocks. The Sr–Nd isotopic compositions for 78 rocks are included. The alkali basaltic volcanism is caused by adiabatic decompression of asthenospheric mantle updomed to a minimum depth of 50 km in connection with the Alpine continent collision. The chemical compositions of the primary basaltic melts from the different areas are similar containing about one hundred-fold enrichment of highly incompatible elements relative to the primitive mantle from partial melting of depleted and secondarily enriched peridotite. The elements Cs, K, Pb and Ti are specifically depleted in the basalts partly because of phlogopite being residual at partial melting. The Tertiary alkali basalts range in Nd-isotopic composition from 0.51288 to 0.51273 and in Sr-isotopic ratios from 0.7032 to 0.7042. These ranges indicate mixtures of HIMU, depleted and enriched mantle components in the metasomatically altered peridotite source which resembles that of certain ocean islands. The Nd-Sr-isotopic compositions of the Quaternary E Eifel are close to bulk Earth ratios. East and W Eifel plots differ distinctly from the Tertiary Hocheifel which is geographically intermediate. This isotopic difference, beside specific K/Na ratios, is probably caused by separate metasomatic pulses that immediately preceded the respective periods of volcanism. The metasomatically altered mantle had partly primitive mantle signatures (Nb/Ta, Zr/Sm and Th/U ratios) and partly ocean island (or MORB) source properties (Rb/Cs). A MORB source can be excluded because of the low K/Rb and high Th/U ratios. A correlation of D with ⁸⁷Sr/⁸⁶Sr in amphibole and phlogopite and a slightly larger ¹⁸O than in MORB is conformable with a seawater and crustal impact on the source of alkali basalts. Slightly higher than average water concentrations in the source of certain primary basaltic melts (indicated by amphibole phenocrysts in their basalts) are required for differentiation of these basalts in magma chambers of the upper crust. Model calculations are presented to explain compositions of differentiates which range from about 60% to about 20% residual melt. The latter are represented by phonolites and trachytes. The Nd- and Sr-isotopic signatures of the majority of differentiates indicate contamination by a granitic partial melt from the wall rocks of magma chambers. Olivine nephelinite magma was the common source of contaminated differentiates.     

Sr-Nd-Pb Isotopic Compositions of Peridotite Xenoliths from Spitsbergen: Numerical Modelling Indicates Sr-Nd Decoupling in the Mantle by Melt Percolation Metasomatism

Several spinel peridotite xenoliths from Spitsbergen have Sr–Ndisotopic compositions that plot to the right of the ‘mantlearray’ defined by oceanic basalts and the DM end-member(depleted mantle, with low ⁸⁷Sr/⁸⁶Sr and high ¹⁴³Nd/¹⁴⁴Nd).These xenoliths also show strong fractionation of elements withsimilar compatibility (e.g. high La/Ce), which cannot be producedby simple mixing of light rare earth element-depleted peridotiteswith ocean island basalt-type or other enriched mantle melts.Numerical simulations of porous melt flow in spinel peridotitesapplied to Sr–Nd isotope compositions indicate that thesefeatures of the Spitsbergen peridotites can be explained bychemical fractionation during metasomatism in the mantle. ‘Chromatographic’effects of melt percolation create a transient zone where thehost depleted peridotites have experienced enrichment in Sr(with a radiogenic isotope composition) but not in Nd, thusproducing Sr–Nd decoupling mainly controlled by partitioncoefficients and abundances of Sr and Nd in the melt and theperidotite. Therefore, Sr–Nd isotope decoupling, earlierreported for some other mantle peridotites worldwide, may bea signature of metasomatic processes rather than a source-relatedcharacteristic, contrary to models that invoke mixing with hypotheticalSr-rich fluids derived from subducted oceanic lithosphere. Pbisotope compositions of the Spitsbergen xenoliths do not appearto be consistently affected by the metasomatism. KEY WORDS: Spitsbergen; lithospheric mantle; metasomatism; radiogenic isotopes; theoretical modelling     

Controls on magmatism in an island arc environment: study of lavas and sub-arc xenoliths from the Tabar–Lihir–Tanga–Feni island chain, Papua New Guinea

The Tabar–Lihir–Tanga–Feni (TLTF) islands of Papua New Guinea mainly comprise high-K calc-alkaline and silica undersaturated alkaline rocks that have geochemical features typical for subduction-related magmatism. Numerous sedimentary, mafic, and ultramafic xenoliths recovered from Tubaf seamount, located on the flank of Lihir Island, provide a unique opportunity to study the elemental and isotopic composition of the crust and mantle wedge beneath the arc and to evaluate their relationships to the arc magmatism in the region. The sedimentary and mafic xenoliths show that the crust under the islands is composed of sedimentary sequences and oceanic crust with Pacific affinity. A majority of the ultramafic xenoliths contain features indicating wide spread metasomatism in the mantle wedge under the TLTF arc. Leaching experiments reveal that the metasomatized ultramafic xenoliths contain discrete labile phases that can account for up to 50% or more of elements such as Cu, Zn, Rb, U, Pb, and light REE (rare-earth elements), most likely introduced in the xenoliths via hydrous fluids released from a subducted slab. The leaching experiments demonstrated that the light REE enrichment pattern can be more or less removed from the metasomatized xenoliths and the residual phases exhibit REE patterns that range from flat to light REE depleted. Sr–Nd isotopic data for the ultramafic residues show a coupled behavior of increasing ⁸⁷Sr/⁸⁶Sr with decreasing ¹⁴³Nd/¹⁴⁴Nd ratios. The labile phases in the ultramafic xenoliths, represented by the leachates, show decoupling between Sr and Nd with distinctly more radiogenic ⁸⁷Sr/⁸⁶Sr than the residues. Both leachates and residues exhibit very wide range in their Pb isotopic compositions, indicating the involvement of three components in the mantle wedge under the TLTF islands. Two of the components can be identified as Pacific Oceanic mantle and Pacific sediments. Some of the ultramafic samples and clinopyroxene separates, however, exhibit relatively low ²⁰⁶Pb/²⁰⁴Pb at elevated ²⁰⁷Pb/²⁰⁴Pb suggesting that the third component is either Indian Ocean-type mantle or Australian subcontinental lithospheric mantle. Geochemical data from the ultramafic xenoliths indicate that although the mantle wedge in the area was extensively metasomatized, it did not significantly contribute to the isotopic and incompatible trace element compositions of TLTF lavas. Compared to the mantle samples, the TLTF lavas have very restricted Pb isotopic compositions that lie within the Pacific MORB range, indicating that magma compositions were dominated by melts released from a stalled subducted slab with Pacific MORB affinity. Interaction of slab melts with depleted peridotitic component in the mantle wedge, followed by crystal fractionation most likely generated the geochemical characteristics of the lavas in the area. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Isotopic relationships of volatile and lithophile trace elements in continental ultramafic xenoliths

The concentrations and isotopic compositions of Sr, Nd, Pb, He and C have been determined for suites of xenoliths from Bullenmerri (Australia), Ichinomegata (Japan), Geronimo (Arizona), and East Africa. The wehrlites and pyroxenites from Bullenmerri have Sr, Nd and Pb isotopic compositions that are generally similar to those found for alkali basalts in the region. The spinel lherzolites, in contrast, have higher ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb and lower ¹⁴³Nd/¹⁴⁴Nd ratios. Whereas the isotopic compositions of He are generally within the range of mid-ocean-ridge basalts (MORB) and do not covary with those of other trace elements, there is an apparent correlation between the ¹³C/¹²C and ¹⁴³Nd/¹⁴⁴Nd ratios for each of the two petrologic groups. These relationships, if substantiated for other xenolith suites, greatly limit the possible mechanisms for generating lithophile and volatile isotopic variations in the continental lithosphere. The helium isotopic compositions for all of the xenoliths fall within the range for MORB. This includes those from Ichinomegata, suggesting that the lower ³He/⁴He ratios found for He sampled at the surface at subduction zones result from mixing mantle He with near-surface crustal He rather than with subducted radiogenic He. Measured C isotopic compositions (relative to Peedee belemnite) for the Ichinomegata xenoliths include values that are both lighter and heavier than those in MORB, and are compatible with contributions from subducted carbon. The Nd and Sr isotopic compositions of the Ichinomegata xenoliths exhibit a correlation over a substantially greater range of values than typically observed for other light-rare-earth-element (LREE)-depleted xenoliths, and include more radiogenic Sr and less radiogenic Nd compositions. The carbon isotopic compositions found for the East African and Geronimo xenoliths extend to values that are lighter than those typically found for MORB.     

Ultramafic Xenoliths in Plio-Pleistocene Alkali Basalts from the Eastern Transylvanian Basin: Depleted Mantle Enriched by Vein Metasomatism

Ultramafic xenoliths from alkali basalts in the Perjani Mountainsin the Eastern Transylvanian Basin (ETB) of Romania are mainlyspinel Iherzolites, although spinel harzburgites, websterites,clinopyroxenites and amphibole pyroxenites are also present.Amphibole veins cut some spinel peridotite samples. All arederived from the shallow lithospheric upper mantle. In general,textural variations are restricted to protogranular and porphyroclastictypes, compared with the more varied textures found in mantlexenoliths from the alkali basalts of the neighbouring PannonianBasin. Also, ETB peridotites are richer in amphibole. Thus,the mantle beneath the edge of the ETB is less deformed butmore strongly metasomatized than the mantle closer to the centreof the Pannonian Basin.Mineralogical and bulk-rock geochemicalvariations resemble those of spinel Iherzolites from other sub-continentalshallow mantle xenolith suites. There is no apparent correlationbetween deformation and geochemistry, and much of the majorand trace element variation is due to variable extraction ofpicritic melts. The REE patterns of separated clinopyroxenesfrom the peridotite xenoliths are mostly LREE depleted, althoughclinopyroxenes from regions adjacent to amphibole veins haveexperienced an enrichment in La and Ce and a change in theirSr and Nd isotopic values towards those of the vein, while stillretaining an overall LREE depletion. Clinopyroxenes from thewebsterites and clinopyroxenites are more variable. Amphibolein the hydrous pyroxenites and amphibole veins is strongly LREEenriched and is considered to be metasomatic in origin. ⁸⁷Sr/⁸⁶Srand ¹⁴³Nd/^l44Nd isotopic ratios of the xenoliths vary between07018 and 07044, and 051355 and 0 51275, respectively. Thesevalue are more depleted than those obtained for xenoliths fromthe Pannonian Basin. The lower ^l43Nd/^l44Nd and higher ⁸⁷Sr/Sr⁸⁶values are found in anhydrous pyroxenites, metasomatic amphibolesin veins and amphibole pyroxenites, and in the only exampleof an equigranular spinel Iherzolite in the suite.The ETB xenolithswere brought to the surface in alkaline vokanism which post-dateda period of Miocene to Pliocene subduction-related cak-alkalinevolcanism. However, the effects of the passage of either slab-derivedfluids or cak-alkaline magmas through the ETB lithospheric mantlecannot be discerned in the chemistry of the xenoliths. The metasomaticamphibole has ⁸⁷Sr/Sr⁸⁶ and ¹⁴³Sr/Sr¹⁴⁴ ratios similar to thehost alkali basalts, but the least evoked cak-alkaline magmasalso have similar Sr and Nd isotope compositions. The REE patternsof the amphibole resembk those of amphiboles considered to havecrystallized from alkaline melts. No preferential enrichmentin elements typically associated with slab-derivedfluids (K,Rb and Sr) relative to elements typically depleted in cak-alkalinemagmas (Ti, 2jr and Nb) has been observed in the vein amphiboles,although some interstitial amphibole is depleted in all incompatibletrace elements, including LREE. Thus, despite its position closeto the calc-alkaline volcanic arc of the Eastern Carpathians,we cannot readily detect any interaction between the lithosphericupper mantle beneath the ETB and subduction-related magmas orfluids. Metasomatism in the lithospheric mantle is instead largelyrelated to the passage of a primitive alkaline magma similarto the host alkali basal ^*corresponding author