Mineralogy and geochemistry of Devonian ultramafic minor intrusions of the southern Kola Peninsula, Russia: implications for the petrogenesis of kimberlites and melilitites

Minor magmatic intrusions of kimberlite, melilitite and cpx-melilitite occur in the southern part of the Kola Peninsula, Russia, on the Terskii Coast and near the town of Kandalaksha. They yield K-Ar ages of 382 ± 14 Ma and 365 ± 16 Ma, similar to the magmatic rocks from the Kola Alkaline Province. The Terskii Coast kimberlites have mineralogical and geochemical affinities with group 1 kimberlites, whereas the Kandalaksha monticellite kimberlite more closely resembles calcite kimberlites. The lower Al₂O₃ content in the Kola kimberlites indicates a strongly depleted harzburgitic source, while higher Al₂O₃ in the melilitites suggests a lherzolitic source. The Terskii Coast kimberlites are anomalously potassic and significantly enriched in P and Ba compared to other group 1 kimberlites. In contrast, the melilitites are sodic and are anomalously depleted in P compared to worldwide melilitites. Trace element patterns of the Kola kimberlites and melilitites indicate the presence of K- and P-rich phases in the mantle source. To account for the K-troughs shown by both magma types, a K-rich phase such as phlogopite is thought to be residual in their sources; however, the anomalous K-enrichment in the Terskii Coast kimberlites may indicate that an additional metasomatic K-rich phase (e.g. K-richterite and/or a complex K-Ba-phosphate) existed in the kimberlite source. The P-depletion in the melilitites may suggest that a phosphate phase such as apatite remained residual in the melilititic source. However, anomalous P-enrichment in the kimberlites cannot be explained by complete melting of the same phase because the kimberlites are a smaller degree melt; thus, it is most likely that another metasomatic phosphate mineral existed in the source of the kimberlites. The Kola kimberlites and melilitites are all strongly LREE-enriched but the kimberlites have a steeper REE pattern and are significantly more depleted in HREE, indicating a higher proportion of garnet in their source. Higher Nb/Y ratios and lower SiO₂ values in the kimberlites indicate that they were a smaller degree partial melt than the melilitites. The presence of diamonds in the Terskii Coast kimberlites indicates a relatively deep origin, while the melilitites originated from shallower depth. The non-diamondiferous Kandalaksha monticellite kimberlite has lower abundances of all incompatible trace elements, suggesting a higher degree of partial melting and/or a less enriched and shallower source than the Terskii Coast kimberlites. The ⁸⁷Sr/⁸⁶Sr_i, ¹⁴³Nd/¹⁴⁴Nd_i and Pb isotope compositions confirm that the Terskii Coast kimberlites have close affinities with group 1 kimberlites and were derived from an asthenospheric mantle source, while the Kandalaksha monticellite kimberlite and Terskii Coast melilitites were derived from lithospheric mantle. Impact of a Devonian asthenospheric mantle plume on the base of the Archaean-Proterozoic lithosphere of the Kola Peninsula caused widespread emplacement of kimberlites, melilitites, ultramafic lamprophyres and other more fractionated alkaline magmas. The nature of the mantle affected by metasomatism associated with the plume and, in particular, the depth of melting and the stability of the metasomatic phases, gave rise to the observed differences between kimberlites and the related melilitites and other magmas. Received: 3 March 1997 / Accepted: 7 October 1997     

Pb-Sr-Nd isotopic compositions and trace element geochemistry of megacrysts and melilitites from the Tertiary Urach volcanic field: source composition of small volume melts under SW Germany

 The Urach volcanic field is unique within the Tertiary–Quaternary European volcanic province (EVP) due to more than 350 tuffaceous diatremes and only sixteen localities with extremely undersaturated olivine melilitite. We report representative Pb-Sr-Nd isotopic compositions and incompatible trace element data for twenty-two pristine augite, Cr-diopside, hornblende, and phlogopite megacryst samples from the diatremes, and seven melilitite whole rocks. The Pb isotopic compositions for melilitites and comagmatic megacrysts have very radiogenic ²⁰⁶Pb/²⁰⁴Pb ratios of 19.4 to 19.9 and plot on the northern hemisphere mantle reference line (NHRL). The data indicate absence of an old crustal component as reflected in the high ²⁰⁷Pb/²⁰⁴Pb ratios of many basalts from the EVP. This inference is supported by ²⁰⁶Pb/²⁰⁴Pb ratios of ∼17.6 to 18.3 and ɛ_Nd of ∼−7.8 to +1.6 for five phlogopite xenocryst samples reflecting a distinct and variably rejuvenated lower Hercynian basement. The ⁸⁷Sr/⁸⁶Sr ratios of 0.7033 to 0.7035 in the comagmatic megacrysts are low relative to their moderately radiogenic Nd isotopic compositions (ɛ_Nd +2.2 to +5.1) and consistent with a long-term source evolution with a low Rb/Sr ratio and depletion in light rare-earth elements (LREE). The melilitite whole-rock data show a similar range in Nd isotopic ratios as determined for the megacrysts but their Sr isotopic compositions are often much more radiogenic due to surface alteration. The REE patterns and incompatible trace element ratios of the melilitites (e.g. Nb/Th, Nb/U, Sr/Nd, P/Nd, Ba/Th, Zr/Hf) are similar to those in ocean island basalts (OIB); negative anomalies for normalized K and Rb concentrations support a concept of melt evolution in the lithospheric mantle. Highly variable Ce/Pb ratios of 29 to 66 are positively correlated with La/Lu, La/K₂O, and Ba/Nd and interpreted to reflect melting in the presence of residual amphibole and phlogopite. The data suggest an origin of the melilitites from a chemical boundary layer very recently enriched by melts from old OIB sources. We suggest that the OIB-like mantle domains represent low-temperature melting heterogeneities in an upwelling asthenosphere under western Europe. Received: 9 March 1995/Accepted: 24 July 1995     

Petrogenesis of Cenozoic Basaltic Rocks from Jiangsu Province,China:Evidence from Geochemical Constraints

Cenozoic（Miocene to Pleistocene） basaltic rocks in Jiangsu province of eastern China include olivine tholeiite and alkali basalt.We present major,trace element and Sr-Nd isotopic data as well as Ar-Ar dating of these basalts to discuss the petrogenesis of the basalts and identify the geological processes beneath the study area.On the basis of chemical compisitions and Ar-Ar dating of Cenonoic basaltic rocks from Jiangsu province,we suggest that these basalts may belong to the same magmatic system.The alkali basalts found in Jiangsu province have higherΣFeO,MgO,CaO,Na₂O, TiO₂ and P₂O₅ and incompatible elements,but lower Al₂O₃ and compatible elements contents than olivine tholeiite which may be caused by fractional crystallization of olivine,pyroxene and minor plagioclase.In Jiangsu basaltic rocks the incompatible elements increase with decreasing MgO/ΣFeO ratios.The primitive mantle-normalized incompatible elements and chondrite-normalized REE patterns of basaltic rocks found in Jiangsu province are similar to those of OIB.Partial loss of the mantle lithosphere accompanied by rising of asthenospheric mantle may accelerate the generation of the basaltic magma.The ¹⁴³Nd/¹⁴⁴Nd vs.⁸⁷Sr/⁸⁶Sr plot indicates a mixing of a depleted asthenospheric mantle source and an EMI component in the study area.According to Shaw’s equation,the basalts from Jiangsu province may be formed by l%-5%partial melting of a depleted asthenospheric mantle source.On the basis of Ar-Ar ages of this study and the fractional crystallization model proposed by Brooks and Nielsen（1982）,we suggest that basalts from Jiangsu province may belong to a magmatic system with JF-2 as the primitive magma which has undergone fractional crystallization and evolved progressively to produce other types of basalts.     

Origin of Ross Island basanitoids and limitations upon the heterogeneity of mantle sources for alkali basalts and nephelinites

Primary basanitoids from Ross Island, Antarctica have REE patterns and Pb isotope ratios similar to those for primary alkali basalts and nephelinites on ocean islands. The lead data from all volcanics on Ross Island have a spread of 4% in the 206/204 ratio and give a two-stage model lead age of 1500 m.y. The age is interpreted to be the time since the development of the chemical heterogeneity of the mantle source, presumably during an earlier melting process. Comparison of REE, K, Rb, Sr, Ba and P₂O₅ concentrations for alkali basalts and nephelinites shows that the chondrite normalized mantle source is enriched in light REE with average La/Sm=3.4, Ce/Sm=2.6, Nd/Sm=1.6. Assuming a mantle source with heavy REE abundances of three times chondrites, nephelinites require 3 to 7% partial melting of the mantle source and alkali basalts require 7 to 15% partial melting. The patterns of K, Cu, V and Ti abundances suggest that phlogopite is a residual mineral for most nephelinite, but not alkali basalt mantle sources, and that a sulfide phase and a titanium-rich mineral are in the residual mantle source for both alkali basalts and nephelinites. Small positive Eu anomalies (2–5%) in near primary alkali basalts and nephelinites suggest that the xxx of the mantle sources is 10^?6 to 10^?9 atm. The progressive enrichment of light REE and incompatible elements in the mantle sources for nephelinites and alkali basalts is proposed to result by intrusion of veins of basaltic melt due to very low percentages of melting 1 000 to 3 000 m.y. ago when this part of the deeper mantle was previously involved in convection and partial melting.     

Origin of coexisting minette and ultramafic breccia,Navajo volcanic field

Trace element evidence indicates that at the Buell Park diatreme, Navajo volcanic field, the felsic minette can be best explained by crystal fractionation from a potassic magma similar in composition to the mafic minettes. Compatible trace element (Cr, Ni, Sc) abundances decrease while concentrations of most incompatible elements (Ce, Yb, Rb, Ba, Sr) remain constant or increase from mafic to felsic minette. In particular, the nearly constant Ce/Yb ratio of the minettes combined with the decrease in Cr, Ni, and Sc abundances from mafic to felsic minette is inconsistent with a model of varying amounts of partial melting as the process to explain minette compositions. The uniformity of rare earth element (REE) abundances in all the minettes requires that an accessory mineral, apatite, dominated the geochemistry of the REE during fractionation. A decrease in P₂O₅ from mafic to felsic minette and the presence of apatite in cognate inclusions are also consistent with apatite fractionation. Higher initial⁸⁷Sr/⁸⁶Sr ratios in the felsic minettes relative to the proposed parental mafic minettes, however, is inconsistent with a simple fractionation model. Also, a separated phlogopite has a higher initial⁸⁷Sr/⁸⁶Sr ratio than host minette. These anomalous isotopic features probably reflect interaction of minette magma with crust.The associated ultramafic breccia at Buell Park is one of the Navajo kimberlites, but REE concentrations of the matrix do not support the kimberlite classification. Although the matrix of the breccia is enriched in the light REE relative to chondrites, and has high La, Rb, Ba, and Sr concentrations relative to peridotites, the concentrations of these elements are significantly lower than in South African kimberlites. A high initial⁸⁷Sr/⁸⁶Sr ratio combined with petrographic evidence of ubiquitous crustal xenoliths in the Navajo kimberlites suggests that the relatively high incompatible element concentrations are due to a crustal component. Apparently, Navajo kimberlites are most likely a mixture of comminuted mantle wall rock and crustal material; there is no evidence for an incompatible element-rich magma which is characteristic of South African kimberlites.If the mafic minettes are primary magmas derived from a garnet peridotite source with chondritic REE abundances, then REE geochemistry requires very small (less than 1%) degrees of melting to explain the minettes. Alternatively, the minettes could have formed by a larger degree of melting of a metasomatized, relatively light REE-enriched garnet peridotite. The important role of phlogopite and apatite in the differentiation of the minettes supports this latter hypothesis.     

Integrated Models of Basalt Petrogenesis: A Study of Quartz Tholeiites to Olivine Melilitites from South Eastern Australia Utilizing Geochemical and Experimental Petrological Data

The Tertiary to Recent basalts of Victoria and Tasmania havemineralogical and major element characteristics of magmas encompassingthe range from quartz tholeiites to olivine melilitites. Abundancesof trace elements such as incompatible elements, including therare earth elements (REE), and the compatible elements Ni, Coand Sc, vary systematically through this compositional spectrum.On the basis of included mantle xenoliths, appropriate 100 Mg/Mg+ Fe₊₂ (68–72) and high Ni contents many of these basaltsrepresent primary magmas (i.e., unmodified partial melts ofmantle peridotite). For fractionated basalts we have derivedmodel primary magma compositions by estimating the compositionalchanges caused by fractional crystallization of olivine andpyroxene at low or moderate pressure. A pyrolite model mantlecomposition has been used to establish and evaluate partialmelting models for these primary magmas. By definition and experimentaltesting the specific pyrolite composition yields parental olivinetholeiite magma similar to that of KilaeauIki, Hawaii (1959–60)and residual harzburgite by 33 per cent melting. It is shownthat a source pyrolite composition differing only in having0.3–0.4 per cent TiO₂ rather than 0.7 per cent TiO₂, isable to yield the spectrum of primary basalts for the Victorian-Tasmanianprovince by 4 per cent to 25 per cent partial melting. The mineralogiesof residual peridotites are consistent with known liquidus phaserelationships of the primary magmas at high pressures and thechemical compositions of residual peridotite are similar tonatural depleted or refractory lherzolites and harzburgites.For low degrees of melting the nature of the liquid and of theresidual peridotite are sensitively dependent on the contentof H₂O, CO₂ and the CO₂/H₂O in the source pyrolite. The melting models have been tested for their ability to accountfor the minor and trace element, particularly the distinctivelyfractionated REE, contents of the primary magmas. A single sourcepyrolite composition can yield the observed minor and traceelement abundances (within at most a factor of 2 and commonlymuch closer) for olivine melilitite (4–6 per cent melt),olivine nephelinite, basanite (5–7 per cent melt), alkaliolivine basalt (11–15 per cent melt), olivine basalt andolivine tholeiite (20–25 per cent melt) provided thatthe source pyrolite was already enriched in strongly incompatibleelements (Ba, Sr, Th, U, LREE) at 6–9 x chondritic abundancesand less enriched (2.5–3 x chondrites) in moderately incompatible(Ti, Zr, Hf, Y, HREE) prior to the partial melting event. Thesources regions for S.E. Australian basalts are similar to thosefor oceanic island basalts (Hawaii, Comores, Iceland, Azores)or for continental and rift-valley basaltic provinces and verydifferent in trace element abundances from the model sourceregions for most mid-ocean ridge basalts. We infer that thismantle heterogeneity has resulted from migration within theupper mantle (LVZ or below the LVZ) of a melt or fluid (H₂O,CO₂-enriched) with incompatible element concentrations similarto those of olivine melilitite, kimberlite or carbonatite. Asa result of this migration, some mantle regions are enrichedin incompatible elements and other areas are depleted. Although it is possible, within the general framework of a lherzolitesource composition, to derive the basanites, olivine nephelinitesand olivine melilitites from a source rock with chondritic relativeREE abundances at 2–5 x chondritic levels, these modelsrequire extremely small degrees of melting (0.4 per cent forolivine melilitite to 1 per cent for basanite). Furthermore,it is not possible to derive the olivine tholeiite magmas fromsource regions with chondritic relative REE abundances withoutconflicting with major element and experimental petrology argumentsrequiring high degrees (15 per cent) of melting and the absenceof residual garnet. If these arguments are disregarded, andpartial melting models are constrained to source regions withchondritic relative REE abundances, then magmas from olivinemelilitites to olivine tholeiites can be modelled if degreesof melting are sufficiently small, e.g., 7 per cent meltingfor olivine tholeiite. However, the source regions must be heterogenousfrom 1 to 5 x chondritic in absolute REE abundances and heterogerieousin other trace elements as well. This model is rejected in favorof the model requiring variation in degree of melting from 4per cent to 25 per cent and mantle source regions ranging fromLREE-enriched to LREE-depleted relative to chondritic REE abundances.     

Geochemistry and origin of the Mirny field kimberlites,Siberia

Here we present new data from a systematic Sr, Nd, O, C isotope and geochemical study of kimberlites of Devonian age Mirny field that are located in the southernmost part of the Siberian diamondiferous province. Major and trace element compositions of the Mirny field kimberlites show a significant compositional variability both between pipes and within one diatreme. They are enriched in incompatible trace elements with La/Yb ratios in the range of (65–300). Initial Nd isotope ratios calculated back to the time of the Mirny field kimberlite emplacement (t = 360 ma) are depleted relative to the chondritic uniform reservoir (CHUR) model being 4 up to 6 ɛNd(t) units, suggesting an asthenospheric source for incompatible elements in kimberlites. Initial Sr isotope ratios are significantly variable, being in the range 0.70387–0.70845, indicating a complex source history and a strong influence of post-magmatic alteration. Four samples have almost identical initial Nd and Sr isotope compositions that are similar to the prevalent mantle (PREMA) reservoir. We propose that the source of the proto-kimberlite melt of the Mirny field kimberlites is the same as that for the majority of ocean island basalts (OIB). The source of the Mirny field kimberlites must possess three main features: It should be enriched with incompatible elements, be depleted in the major elements (Si, Al, Fe and Ti) and heavy rare earth elements (REE) and it should retain the asthenospheric Nd isotope composition. A two-stage model of kimberlite melt formation can fulfil those requirements. The intrusion of small bodies of this proto-kimberlite melt into lithospheric mantle forms a veined heterogeneously enriched source through fractional crystallization and metasomatism of adjacent peridotites. Re-melting of this source shortly after it was metasomatically enriched produced the kimberlite melt. The chemistry, mineralogy and diamond grade of each particular kimberlite are strongly dependent on the character of the heterogeneous source part from which they melted and ascended.

     

Tertiary basalts and peridotite xenoliths from the Hessian Depression (NW Germany), reflecting mantle compositions low in radiogenic Nd and Sr

A total of 17 alkali basalts (alkali olivine basalt, limburgite, olivine nephelinite) and quartz tholeiites, and of 10 peridotite xenoliths (or their clinopyroxenes) were analyzed for Nd and Sr isotopes. ¹⁴³Nd/¹⁴⁴Nd ratios and ⁸⁷Sr/⁸⁶Sr ratios of all basalts and of the majority of ultramafic xenoliths plot below the mantle array with a large variation in Nd isotopes and a smaller variation in Sr isotopes. The tholeiites were less radiogenic in Nd than the alkali basalts. Volcanics from the Eifel and Massif Central regions contain Nd and Sr, which is more radiogenic than that of the basalts from the Hessian Depression. Nd and Sr isotopic compositions of all rocks from the latter area, with the exception of one tholeiite and one peridotite plot in the same field of isotope ratios as the Ronda ultramafic tectonite (SW Spain), which ranges in composition from garnet to plagioclase peridotite. The alkali basaltic rocks are products of smaller degrees of partial melting of depleted peridotite, which has undergone a larger metasomatic alteration compared with the source rock of tholeiitic magmas. For the peridotite xenoliths such metasomatic alteration is indicated by the correlation of their K contents and isotopic compositions. We assume that the upper mantle locally can acquire isotopic signatures low in radiogenic Nd and Sr from the introduction of delaminated crust. Such granulites low in radiogenic Nd and Sr are products of early REE fractionation and granite (Rb) separation.     

岚皋早古生代碱质煌斑杂岩地球化学特征及成因探讨

岚皋碱质煌斑杂岩主量元素呈规律性演化，REE球粒陨石标准化配分型式呈强右倾型，富集不相容元素。岩石主元素和微量元素地球化学特征表明，煌斑岩浆在演化过程中存在2个平行的结晶分异演化趋势，岩浆演化过程中受地壳混染的程度很小。LREE、不相容元素的强烈富集及Dy／Yb、La／Yb、Zr／Sm、Ce／Y等微量元素的质量分数比值变化表明，煌斑杂岩不可能由尖晶石或石榴石二辉橄榄岩、含角闪石的尖晶石或石榴石二辉橄榄岩的部分熔融形成，它的源区应为含金云母和单斜辉石的交代地幔。Sr-Nd-Pb同位素结果显示，煌斑岩浆源区的地幔主要为HIMU端元组分。地幔柱的活动与煌斑岩浆的起源密切相关，并制约了其源区的地幔交代作用。     

REE compositional characteristics of Hannuoba basalts

The Hannuoba basalts are a suite of associated rocks consisting of alkali basalts and tholeiites. The alkali basalts can be divided into the K-rich type and the Na-rich type, while the tholeiites are almost solely of the Na-rich type. These two types of basalt are characterized as being obviously rich in light rare earth elements, as is shown in the chondrite-normalized REE patterns exhibiting positive Eu anomalies. However, significant differences in (La / Yb)_N and Eu / Eu* ratios are noticed between these two types of basalt. They seem to have been derived from varying-degree partial melting of mantle rocks.     

Case studies on the origin of basalt

The simplified model of basalt genesis described in Part I of this series, equilibrium partial melting followed by Rayleigh-type fractional crystallization, is applied to a stratigraphically controlled sequence of basalt flows from Kohala volcano. Major-element compositions were determined for 52 samples and show a time-stratigraphic progression from tholeiites through transitional basalts to alkali basalts. Twenty-six of these samples were analyzed by isotope dilution for K, Rb, Cs, Sr, Ba and the REE, 13 for⁸⁷Sr/⁸⁶Sr, and 19 for Co, Cr, Ni and V by atomic absorption. After a simple, first-order correction for the effects of fractional crystallization (involving mostly olivine and aluminous clinopyroxene), the major element concentrations cluster tightly, and the incompatible trace elements show monotonic increases in concentration as a function of stratigraphic height. The process identification plot shows that all the (fractionation corrected) melt compositions can be explained by equilibrium partial melting of compositionally identical batches of source material. The REE and Sr are fractionated because of the presence of residual clinopyroxene. Garnet may also be present but in much smaller amounts. In this respect our results differ significantly from those of Leeman et al. (1980). The calculated chondrite-normalized REE patterns of the source are nearly flat to slightly convex upward. Therefore there is no need to invoke special mechanisms, such as metasomatic REE preenrichment of the source, in order to explain the petrogenesis of the suite of lavas. Specifically, Ce concentrations ranging from 20 to 250 times chondritic are all explained by the same calculated source pattern having a chondrite-normalized ratio of Ce/Sm=0.9±0.2. However, the normalized ratio Ce/Ba?2 shows that the source is not simply primitive mantle.     

Trace Element Geochemistry of Tertiary Continental Alkali Basalts from the Liuhe—Yizheng Area,Jiangsu Province,China

Reported in this paper are the chemical compositions and trace element (REE,Ba,Rb,Sr,Nb,Zr,Ni,Cr,V,Ga,Y,Sc,Zn,Cu,etc)abundances of Tertiary continental alkali basalts from the Liube-yizheng area,Jiangsu Province,China.The olivine basalt,alkali olivine basalt and basanite are all derived from evolved melts which were once af-fected by different degrees of fractional crystallization of olivine and clinopyroxene(1:2)under high pres-sures.The initial melts were derived from the garnet lherzolite-type mantle source through low-degree par-tial melting.The mantle source has been affected by recent mantle-enrichment events(e.g.mantle metasomatism),resulting in incompatible trace element enrichment and long-term depletion of radiogenic isotopic compositions of Sr and Nd.     

Geochemistry and Petrology of Emeishan Basalts and Subcontinental Mantle Evolution in Southwestern China

Three major volcanic rock sequences in the P2β formation(Emeishan basalts)were sampled dur-ing a comprehensive study of the Late Permian volcanics associated with the Panxi paleorift in southwestern China .Two of the three sections-Emei and Tangfang are composed of continental flood basalts(CFB) while the third-Ertan is an alkalic center.Multi-element chemical analyses indi-cate a predominance of low MgO transitional quartz tholeiites at Emei and Tangfang,whereas the Ertan suite ranges from high-MgO alkaline olivine basalts to rhombic porphyry trachytes and quartz-bearing aegerine-augite syenites.Consanguineity of the rocks from the three sections is sug-gested by consistently high TiO2 ,K2O,incompatible trace elements and uniformly fractionated REE patterns typical of alkalic compositions,but antypical of CFB.Sr isotope data for ten Emei basalt samples(^87Sr/^86Sr=0.7066-0.7082)which show no correla-tion with Rb/Sr ratios (0.02-0.12) and Nd isotopes for two of the samples(^143Nd/^144Nd=0.51171-0.51174)are interpreted as being related to the mantle evolution.The primary magmas re-sponsible for all the three sequences have been modeled in terms of a uniformly metasomatized man-tle source.Trace element models support the derivation of the Emei and Tangfang primary magmas from 10-15 percent partial melting of spinel lherzolite,followed by fractional crystallization of olivive and clinopyroxene.The primary alkaline olivine basalts at Ertan are generated by 7-10 percent par-tial melting of a chemically equivalent source in the garnet-peridodite stability region.The assumed mantle composition is characterixzed by Rb=3.8-5.5 ppm,Sr=62-83ppm,Ba=45-64 ppm,La=3.8-5.6ppm,and Yb=0.46-0.57ppm.The proposed mechanism of regional mantle enrichment requires metasomatic stabilization of phlogopite which becomes depleted later during par-tial melting.Such enrichment is consistent with the models proposed for alkalic systems in which a large mantle diaper acts as the agent for upward enrichment as well as uplift and extension of the crust.     

Compositional heterogeneity of the continental lithospheric mantle beneath the Early Precambrian and Phanerozoic structures: Evidence from mantle xenoliths in kimberlites and alkaline basalts

Data on the petro- and geochemical characteristics of mantle xenoliths in kimberlites, which sampled the mantle beneath Early Precambrian tectonic structures (Archean cratons: the basement of the Eastern Siberian Platform, Karelian, Kaapvaal, Wyoming, Western Dharvar; Early and Middle Proterozoic foldbelts: Western Olenek, Natal, and Halls Creek), and xenoliths in alkaline basalts, which sampled the mantle benath Late Proterozoic-Phanerozoic structures (foldbelts: Central Asian, Mozambique, southern tip of South America, and Central German) indicate the following: (1) The major and trace element and REE composition of the mantle is different beneath Early Precambrian structures and Late Proterozoic-Phanerozoic foldbelts and reflects the degree of partial melting of the primitive mantle and its depletion in magmaphile components beneath ancient structures compared to young ones. (2) The original composition of the mantle was different beneath the Early Precambrian and Late Proterozoic structures in terms of both major oxides and incompatible trace elements and REE and their ratios; the composition of the mantle beneath the Eastern Siberian Platform, Wyoming, and Karelian cratons is different in terms of Zr/Y, La/Sm, Ce/Sm, Gd/Yb, and Lu/Hf. (3) The degree of melting of the primitive mantle decreases with depth, as follows from the negative correlation between the MgO/SiO₂ ratio and pressure (i.e., depth) and the positive correlation between the Al₂O₃/MgO ratio and pressure in the xenoliths. (4) The Y, Zr, Ti, Sm, Gd, and Yb conncentrations and the sum of HREE in the mantle decrease with increasing degree of melting; correspondingly, the material most strongly depleted in these incompatible trace elements and REE composes the upper levels of the lithospheric continental mantle.     

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.     

Cretaceous alkaline lamprophyres from northeastern Czech Republic: geochemistry and petrogenesis

The northeast part of the Czech Republic (Moravia) and the adjoining part of Poland host a 100-km-long and 15- to 25-km-wide belt containing numerous isolated bodies (mainly sills) of lamprophyre of Lower Cretaceous age. The lamprophyres range from mafic (melanocratic) to evolved, feldspar-rich (mesocratic) variants. Mineralogically, they are characterized by compositionally zoned kaersutite phenocrysts, biotite and high Al–Ti salitic to diopsidic clinopyroxene. The lamprophyres are typically alkaline as shown by high contents of P₂O₅, TiO₂, alkalies and incompatible trace elements such as light REE, Zr, Nb, Y, Ba and Sr, and by high Ti/V (>50) and chondrite-normalized (La/Yb)_n (8–25) ratios. They resemble alkali basalts, basanites and nephelinites. Major element composition and trace element patterns and Nd–Sr isotopic values (εNd ca. +5.5 to +6.6 and εSr ca. –9.5 to –24.0) indicate that the lamprophyric magma was derived from a mantle source that was compositionally similar to the source of ocean island basalts with HIMU affinities and some continental extension-related alkali basaltic suites. The lamprophyres do not show any subduction imprint. They were generated in the garnet stability field by a variable degree of melting. Evolved lamprophyres were formed by clinopyroxene-dominated fractional crystallization of mafic lamprophyric magma. The lamprophyres are interpreted to have been emplaced along conduits formed during the formation of a basin/graben structure in the Early Cretaceous.     

Petrology and geochemistry of diamondiferous Mesoproterozoic kimberlites from Wajrakarur kimberlite field,Eastern Dharwar craton,southern India: genesis and constraints on mantle source regions

The petrology and geochemistry of some new occurrences of Mesoproterozoic diamondiferous hypabyssal-facies kimberlites from the Chigicherla, Wajrakarur-Lattavaram and Kalyandurg clusters of the Wajrakarur kimberlite field (WKF), Eastern Dharwar craton (EDC), southern India, are reported. The kimberlites contain two generations of olivine, and multiple groundmass phases including phlogopite, spinel, calcite, dolomite, apatite, perovskite, apatite and rare titanite, and xenocrysts of eclogitic garnet and picro-ilmenite. Since many of the silicate minerals in these kimberlites have been subjected to carbonisation and alteration, the compositions of the groundmass oxide minerals play a crucial role in their characterisation and in understanding melt compositions. While there is no evidence for significant crustal contamination in these kimberlites, some limited effects of ilmenite entrainment are evident in samples from the Kalyandurg cluster. Geochemical studies reveal that the WKF kimberlites are less differentiated and more primitive than those from the Narayanpet kimberlite field (NKF), Eastern Dharwar craton. Highly fractionated (La/Yb = 108–145) chondrite-normalised distribution patterns with La abundances of 500–1,000 × chondrite and low heavy rare earth elements (HREE) abundances of 5–10 × chondrite are characteristic of these rocks. Metasomatism by percolating melts from the convecting mantle, rather than by subduction-related processes, is inferred to have occurred in their source regions based on incompatible element signatures. While the majority of the Eastern Dharwar craton kimberlites are similar to the Group I kimberlites of southern Africa in terms of petrology, geochemistry and Sr–Nd isotope systematics, others show the geochemical traits of Group II kimberlites or an overlap between Group I and II kimberlites. Rare earth element (REE)-based semi-quantitative forward modelling of batch melting of southern African Group I and II kimberlite source compositions involving a metasomatised garnet lherzolite and very low degrees of partial melting demonstrate that (1) WKF and NKF kimberlites display a relatively far greater range in the degree of melting than those from the on-craton occurrences from southern Africa and are similar to that of world-wide melilitites, (2) different degrees of partial melting of a common source cannot account for the genesis of all the EDC kimberlites, (3) multiple and highly heterogeneous kimberlite sources involve in the sub-continental lithospheric mantle (SCLM) in the Eastern Dharwar craton and (4) WKF and NKF kimberlites generation is a resultant of complex interplay between the heterogeneous sources and their different degrees of partial melting. These observations are consistent with the recent results obtained from inversion modelling of REE concentrations from EDC kimberlites in that both the forward as wells as inverse melting models necessitate a dominantly lithospheric, and not asthenospheric, mantle source regions. The invading metasomatic (enriching) melts percolating from the convecting (asthenosphere) mantle impart an OIB-like isotopic signature to the final melt products.     

Tholeiitic and alkali basalts from the Mid-Atlantic Ridge at 43 ° N

Tholeiitic basalts dredged from the Mid-Atlantic Ridge (MAR) axis at 43 ° N are enriched in incompatible trace elements compared to the ‘ normal’ incompatible element depleted tholeiites found from 49 ° N to 59 ° N and south of 33 ° N on the MAR. The most primitive 43 ° N glasses have MgO/FeO*= 1.2 and coexist with olivine (Fo_90–91) and chrome-rich spinel. The tholeiitic basalts from the MAR 43 ° N are distinct from the strongly incompatible trace element depleted tholeiities found elsewhere in the Atlantic, and have trace element features typical of island tholeiities and MAR axis tholeiites from 45 ° N. Petrographic, major, and compatible trace element trends of the axial valley tholeiites at 43 ° N are consistent with shallow-level fractionation; in particular, evolution from primitive liquids with forsteritic olivine plus chrome spinel as liquidus phases to fractionated liquids with plagioclase plus clinopyroxene as major crystallizing phases. However, each dredge haul has distinctive incompatible trace element abundances. These trace element characteristics require a hetrogeneous mantle or complex processes such as open system fractional crystallization and magma mixing. Alkali basalts (～5% normative nepheline) were dredged from a prominent fracture zone at 43 ° N. Typical of alkali basalts they are strongly enriched (compared to tholeiites) in incompatible elements. Their highly fractionated rare-earth element (REE) abundances require residual garnet during partial melting. The 43 ° N tholeiites and alkali basalts could be derived from a garnet peridotite source with REE contents equal to 2 × chondrites by ～5% and 1% melting, respectively. Alternatively, they could be derived from a moderately light REE enriched source by ～25% and 9.5% melting, respectively.     

Subduction—Modified Subcontinental Mantle in South China：Trace Element and Isotope Evidence in Basalts from Hainan Island

Cenozoic lavas from Hainan Island,South China,comprise quartz tholeiite,olivine tholeiite,alkali basalt,and basanite and form a continuous,tholeiite-dominated,compositional spectrum.Highly incompatible elements and their relationships with isotopes in these lavas are shown to be useful in evaluating mantle-source composition,whereas modeling suggests that ratios of elements with bulk partition coefficients significantly larger than those of Nb and Ta may be sensitive to partial melting.Th/Ta and La/Nb ratios of alkali basalts are lower than those of tholeiites,and they are all lower than those of the primitive mantle,These ratios correlate positively with ^207Pb/^204Pb and ^87Sr/^86Sr ratios.Such relationships can be explained by mixing of depleted and enriched source components.A depleted component is indicated by alkali basalt compositions and is similar to some depleted OIB (PREMA).The enriched component,similar to sediment compositions,is indicated by tholeiites with high LILE/HFSE,^207Pb/^204Pb,and ^87Sr/^86Sr ratios.In general,basalts from Hainan and the South China Basin(SCB)share common geochemical characters.e.g.high Rb/Sr,Th/Ta,^207Pb/^206Pb,and low Ba/Th ratios.Such a geochemical trend is comparable to that of EMII-type OIB and best explained as the result of subduction.Occurrence of these characteristics in both continental Hainan basalts and SCB seamout basalts indicates the presence of a South China geochemical domain that exists in the mantle region below the lithosphere.     

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.