Variation in the geochemistry of mantle sources for tholeiitic and calc-alkaline mafic magmas,Western Sunda volcanic arc,Indonesia

Quaternary lavas of the normal island-arc basalt—andesite—dacite association in the islands of Java and Bali range from those belonging to tholeiitic series over Benioff-zone depths of ～ 150 km to high-K calc-alkaline series over Benioff-zone depths of 250 km. More abundant and diverse calc-alkaline lavas are found over intermediate Benioff-zone depths. On average, basaltic lavas become slightly more alkaline (largely due to increased K contents) with increasing depth to the Benioff zone. Levels of incompatible minor and trace elements (K, Rb, Cs, Ba, Nb, U, Th, light REE) show a corresponding increase of almost an order of magnitude.Low average Mg-numbers (～ 0.52) and Ni and Cr abundances (15–25 and 35–60 ppm, respectively) of basaltic lavas suggest that few lavas representing primary mantle-derived magma compositions are present. Calculated primary basaltic magma compositions for most tholeiitic and calc-alkaline volcanic centres are olivine tholeiites with 15–30% ol. The single high-K calc-alkaline centre considered yielded transitional alkali olivine basalt—basanite primary magma compositions. These calculated magma compositions suggest that the percentage of mantle melting decreases with increasing depth to the Benioff zone (from >25 to <10%), while the corresponding depth of magma separation increases from ～ 30 to 60 km.Calculation of REE patterns for basaltic magmas on the basis of peridotitic mantle sources with spinel lherzolite, amphibole lherzolite or garnet lherzolite mineralogy, and model REE levels of twice chondritic abundances, indicates that change in the conditions of magma genesis alone cannot explain the observed change in light-REE abundances of basaltic lavas with increasing depth to the Benioff zone. Complementary calculations of the REE levels of mantle sources required to yield the average tholeiitic, calc-alkaline and high-K calc-alkaline basaltic magma indicate that light-REE abundances must increase from 2–3 to 7–8 times chondrites with increasing depth to the Benioff zone. The percentages of mantle melting favoured on REE evidence are lower than those indicated by major-element considerations.The observed variation in incompatible element geochemistry of mantle magma sources is thought to be related directly or indirectly to dehydration and partial-melting processes affecting subducted oceanic crust. The possible nature of this relationship is discussed.     

The origin of basaltic rocks in Niutoushan area— high pressure differentiation

The Niutoushan basaltic cone, consisting of subalkali (quartz-tholeiite and olivine-tholeiite) and alkali basalts, is Late Tertiary in age. Its major characteristics are generalized as follows:

1. Both early subalkali and late alkali bali basalts are formed under the same geological environment.
2. The continuity in chemical composition from subalkali to alkali and the low FeO/MgO in alkali basalts show that they are the products of cognate magmatic differentiation.
3. The change from low REE abundance and weak enrichment of LREE in subalkali to high REE abundance and strong enrichment of LREE in alkali basalts indicates obvious REE enrichment and fractionation during magmatic differentiation. Weak positive Eu anomalies in the REE patterns are indicative of their formation under low oxygen fugacity conditions.
4. According to the calculated values, 70–75% of the primary olivine tholeiitic magma had been separated as subalkaline basaltic magma, the rest residual magma became alkaline basaltic magma. This result is consistent to the field observation that the outcrop area of subalkali basalts is four times as much as that of alkali basalts.
5. The basaltic rocks of Niutoushan show an S-type distribution straddling the thermal barrier on Ol′-Ne′-Qu′ diagram and an evolution tendency for Ne to increase with increasing FeO/MgO. This is in agreement with the melting experimental data on olivine basalts at 10–20 kb.
6. Mantle-derived inclusions (spinel lherzolite) in this area occur in both alkali olivine basalts and olivine tholeiites. The latter is of extremely rare occurrence. The formation temperature and pressure of the inclusions in alkalibasalts and olivine tholeiites have been calculated. The results show that the alkaline basaltic magma was separated from the subalkaline basaltic magma at about 20 kb.

Basaltic rocks in Niutoushan were formed through the so-called “high pressure differentiation”, that is, at about 20 kb the crystallization of clinopyroxene and orthpyroxene resulted in the separation of subalkaline basaltic magma from the primary olivine tholeiitic magma, and then the residue gradually became alkaline olivine basaltic magma.     

中国东部新生代玄武岩稀土配分的分形结构因子与其它化学组成的相关性

本文提出了稀土配分分形结构因子概念和计算方法。利用这个新方法，计算了中国东部新生代玄武岩中稀土配分的分形结构因子。研究了这些因子与玄武岩主元素、稀土元素、分散元素和同位素之间的关系，并求出了其相关性参数。利用这些参数，求出了两个端元玄武岩的主元素和稀土元素含量；提出了五大莲池地区玄武岩可能与富钾交代地幔部分熔融作用有关，其它玄武岩的形成与软流圈地幔或岩石圈地幔部分熔融有关；玄武岩同位素的比值不仅受玄武岩浆地幔源区本身的特征制约，还可能受地幔岩部分熔融程度的制约。     

我国东部新生代玄武岩岩石化学的一些探讨

新生代是地球上玄武质岩浆的主要活动期。在我国东部,新生代玄武岩分布也极广泛,由北往南自大兴安岭、松辽盆地经华北、苏闽浙至台湾、海南岛以及近海大陆架均有不同程度的出露。时间上从老第三纪至史期均有玄武岩喷发活动。     

Ages,rare-earth element enrichment,and petrogenesis of tholeiitic and alkalic basalts from Kahoolawe Island,Hawaii

Kahoolawe Island, Hawaii (18×11 km), is a basaltic shield volcano with caldera-filling lavas, seven identified postshield vents, and at least two occurrences of apparent rejuvenated-stage eruptive. We examined 42 samples that represent all stages of Kahoolawe volcano stratigraphy for their petrography, whole-rock major-and trace-element contents, mineral compositions, and K–Ar ages. The two oldest shield samples have an average age of 1.34±0.08 Ma, and four postshield samples (3 are alkalic) average 1.15±0.03 Ma; ages of 1.08 and 0.99 Ma for two additional tholeiitic samples probably are minimum ages. Whole-rock major- and trace-element and mineral compositions of Kahoolawe shield and caldera-fill laves are generally similar to the lavas forming Kilauea and Mauna Loa tholeiitic shields, but in detail, Kahoolawe shield lavas have distinctive compositions. An unusual aspect of many postshield Ka-hoolawe lavas is anomalously high REE and Y abundances (up to 200 ppm La and 175 ppm Y) and negative Ce anomalies. These enrichments reflect surficial processes, where weathering and soil development promoted REE-Y transport at the weathering front. Major element abundances (MgO, 10–6 wt.%) for shield and caldera-fill basalts are consistent with fractionation of ol+px+pl in frequently replenished magma reservoirs. In general, tholeiitic basalts erupted from late vents are higher in SiO₂ than the shield lavas, and temporal differences in parental magma compositions are the likely explanation. Alkalic basalts that erupted from vents are comparable in composition to those at other Hawaiian volcanoes. Trace-element abundance ratios indicate that alkalic basalts represent either relatively lower degrees of melting of the shield source or a distinct source. Apparent rejuvenated-stage basalts (i.e., emplaced after substantial Kahoolawe erosion) are tholeiitic, unlike the rejuvenated-stages at other Hawaiian volcanoes (alkalic). Kahoolawe, like several other Hawaiian volcanoes, has intercalated tholeiitic and alkalic basalts in the postshield stage, but it is the only volcano that appears to have produced tholeiitic rejuvenated-stage lavas.     

Evidence for the role of phlogopite in the genesis of alkali basalts

Evaluation of available experimental and petrochemical evidence suggests that variations of potassium, titanium and aluminium in basalts can be explained by the melting of titaniferous phlogopite at depths exceeding about 60 km in the upper mantle. For tholeiitic basalts, an inverse covariance is recognised between titanium and aluminium which is probably controlled by the depth of magma segregation. The relative effects of pressure and phlogopite breakdown have been estimated for selected suites of alkali basalt.     

汉诺坝玄武岩化学及其演化趋势

汉诺坝玄武岩于中新世喷出。除了碱性玄武岩以外,夏威夷岩广泛分布,还有苦橄玄武岩和马盖尔岩。有三个岩浆演化趋势:地壳岩浆房内橄榄石和单斜辉石斑晶组合的分离作用产生了从夏威夷岩到马盖尔岩的肯尼迪分异趋势;莫霍面附近的岩浆房内石榴石、普通辉石、歪长石和钛铁矿巨晶组合的分离作用导致了由原生夏威夷岩和碱性玄武岩经过进化的夏威夷岩和碱性玄武岩到拉斑玄武岩的跨式B型分异趋势;原生岩浆演化趋势。     

Evolution of major mineral compositions and trace element abundances during fractional crystallization of a model lunar composition

The evolution of major mineral compositions and trace element abundances during fractional crystallization of a model lunar magma ocean have been calculated. A lunar bulk composition consistent with petrological constraints has been selected. Major mineral compositions have been calculated using published studies of olivine-melt, plagioclase-melt, and pyroxene-olivine equilibria. Trace element abundances have been calculated using experimentally-determined partition coefficients where possible. In the absence of experimental determinations, published partition coefficients obtained by analyzing phase separates from porphyritic volcanic rocks have been used. Trace elements studied are La, Sm, Eu, Lu, Rb, Sr( Eu²⁺), Ni, Co, and Cr.The first mineral to crystallize is olivine, which varies in composition from Fo₉₈ at the liquidus to Fo₉₅ at 50% solidification. Orthopyroxene crystallizes from 50 to 60% solidification with a restricted composition range of En₉₅-En₉₃. Plagioclase and Ca-rich clinopyroxene (X_Wo arbitrarily set equal to 0.5) co-crystallize during the final 40% solidification. Plagioclase changes in composition from An₉₇ to approximately An₉₃, while clinopyroxene evolves from En₄₆ to approximately En₄₀. The concomitant evolution of major element abundances in the melt is also discussed.The concentration of Ni in the melt decreases rapidly because solid-melt partition coefficients are significantly greater than unity at all stages of crystallization. The concentration of Cr in the melt increases slowly during olivine crystallization, then drops precipitously during the crystallization of orthopyroxene and clinopyroxene. The concentration of Co in the melt decreases slowly during olivine and orthopyroxene crystallization, after which it returns slowly to its initial concentration. Rubidium and Sr are not fractionated relative to one another until the onset of plagioclase crystallization. Ratios of Rb/Sr, normalized to their initial concentrations in the magma, do not rise above 10 until 95% of the magma has solidified. The ratios of Eu/Sm and La/Lu, normalized to their initial concentrations in the magma, remain essentially unfractionated until the onset of crystallization of clinopyroxene plus plagioclase, at which point the normalized La/Lu ratio increases to approximately 1.3 at 100% solidification and the normalized Eu/Sm ratio decreases to approximately 0.2 at 100% solidification.The model calculations are used to place approximate constraints on the bulk composition of the primitive Moon. Consideration of the effect on plagioclase composition of the activities of NaO_0.5 and SiO₂ in the melt suggests that the primitive Moon contained less than 0.4 wt % NaO_0.5 and approximately 42–43 wt % SiO₂. Concentrations of the REE in model lunar anorthosites are consistent with the returned samples. Concentrations of the REE in several model ‘highland basalts’ (considered to be representative of the average lunar terrae) are too low when compared with returned samples. Several possible explanations of this discrepancy are considered. The possible role of spinel in a twostage geochemical evolution of mare basalt liquids is discussed.     

A Study on the Forming Conditions of Basalts in Seamounts of the South China Sea

Volcanic rocks in seamounts of the South China Sea consist mainly of alkali basalt, tholeiitic basalt, trachyandesitic pumice, dacite, etc. Inclusions in the minerals of the volcanic rocks are mainly amorphous melt inclusions, which reflects that the volcanic rocks are characterized by submarine eruption and rapid cooling on the seafloor. Furthermore, fluid-melt inclusions have been discovered for the first time in alkali basalts and mantle-derived xenoliths. indicating a process of differentiation between magma and fluid in the course of mantle partial melting. Alkali basalts and inclusions may have been formed in this nonhomogeneous system. Rock-forming temperatures of four seamounts were estimated as follows: the Zhongnan seamount alkali basalt 1155 ∼ 1185 °C; the Xianbei seamount alkali basalt 960 ∼ 1200 °C; tholeiitic basalt 1040 ∼ 1230 °C; the Daimao seamount tholeiitic basalt 1245 ∼ 1280 °C; and the Jianfeng seamount trachyandestic pumice 880 ∼ 1140 °C. Equilibrium pressures of alkali basalts in the Zhongnan and Xianbei seamounts are 13.57 and 8.8 × 10⁸ Pa, respectively. Pyroxene equilibrium temperatures of mantle xenoliths from the Xianbei seamount were estimated at 1073 ∼ 1121 °C, and pressures at (15.58 ∼ 22.47)×10⁸Pa, suggesting a deep-source (e.g. the asthenosphere) for the alkali basalts. This project was financially supported by the National Natural Science Foundation of China and Guangzhou Marine Geology Survey.     

Mobility of Rare Earth Elements in Basalt‐Derived Laterite at the Bolaven Plateau,Southern Laos

Geochemical and geochronological studies were conducted on basalts and laterites from the Bolaven Plateau in southern Laos in order to evaluate the mobility and mineralization of REE, Y and Sc during laterization. The basalts are classified into three categories: (i) small volumetric alkali basalt (eruption age: 15.7 Ma), large volumetric olivine tholeiite (1.2 Ma) and quartz tholeiite with olivine tholeiite (younger than 0.5 ± 0.2 Ma). Formation of REE minerals during laterization result in mobilization and fractionation of REE and Y in laterite profiles. Occurrence of florencite‐(Ce) in a laterite profile derived from alkali basalt immobilizes REE (particularly LREE) and this leads the laterites to be enriched in LREE relative to the parent basalt. Few positive Ce anomalies in this profile suggest that florencite‐(Ce) [(Ce)Al₃(PO₄)₂(OH)₂] formation was followed by CeO₂ precipitation due to the change of redox condition. In tholeiite‐derived laterite profiles, florencite is not recognized and REE and Y tend to be depleted relative to the parent basalts with positive Ce anomalies. This is interpreted as scavenging REE³⁺ except for Ce⁴⁺ from the laterite profile in oxidizing conditions. Sc behaves similarly to Fe during laterization and it is more abundant in the tholeiitic laterite than that in the alkali basaltic laterite. Results of sequential extraction indicate that REE of the alkali basaltic laterite are contained in residual phase, which is dominantly florencite‐(Ce), but they are rarely present in ion‐adsorption phase. It is concluded that basaltic laterites have a low potential of REE resource in terms of low REE contents and a difficulty in REE extraction.     

Petrologic implications of trace element variation in clinopyroxene megacrysts from the Nógrád volcanic province, north Hungary: a study by laser ablation microprobe-inductively coupled plasma-mass spectrometry

Clinopyroxene megacrysts in alkali basalts are an important source of information about the evolution of magmatic systems at depth. In this study, we have undertaken a detailed examination of the trace element contents in a suite of megacrysts from 2.5 Ma old alkali basalts in the Nógrád volcanic province of Hungary and Slovakia. The megacrysts range in composition from Mg-rich and in equilibrium with their host magmas, to those that are Fe-rich and must have evolved in more fractionated magmas. The conditions of crystallization of these megacrysts, as calculated from the Al^VI/Al^IV ratios, suggests they all formed at about 30 km, or the crust–mantle boundary in this area. Using the most magnesian megacrysts and compositions of the host lavas, we have calculated the partition coefficients for a range of trace elements. However, the trace element contents in the megacrysts show a systematic variation with major element composition. Moreover, the rate of increase or change in the trace element concentrations is not consistent with models involving constant or steady state partition coefficients. Using a series of assumptions and models, we hypothesize that the partition coefficients between clinopyroxene and melt change substantially during the magmatic evolution of the system. This change is not constant for each element group, with the high field strength elements showing the most substantial increases. Electrostatic charge balance may have been the most important factor in controlling the mineral/melt partitioning.     

Petrology and geochemistry of komatiites and tholeiites from Gorgona Island,Colombia

Komatiitic rocks from Gorgona Island, Colombia, in contrast to their Archaean counterparts, occur as rather structureless flows. In addition, textural and mineralogical features indicate that the Gorgona komatiites may have crystallized from superheated liquids. Komatiitic rocks have MgO contents which range from 24 to 11 wt.% and plot on well-defined olivine (Fo₉₀) control lines. Calculations show that potential evolved liquids (MgO<11 wt%) will be SiO₂-poor. Komatiites, in this case, cannot be regarded as parental to the associated tholeiitic basalt sequence.On the basis of REE concentrations and Sr, Nd isotopic compositions, the associated basalts are found to be of two types. One type (K-tholeiite) is characterized by noticeably fractionated REE patterns and relatively primitive isotopic compositions similar to those of the komatiites. K-tholeiites, together with komatiites, are regarded as comprising a distinctive komatiitic suite. REE patterns within this suite show progressive depletion in the LREE from K-tholeiites to komatiites, and represent increasingly higher degrees of melting of the same mantle source region. The other type (T-tholeiite), representative of the bulk of the exposed basalt sequence, has flat REE patterns and relatively evolved isotopic compositions. This tholeiitic suite is clearly genetically unrelated to the komatiitic suite.     

REE Abundaces in Megacrysts and Host Basalts：REE Behavior of Magma at High Pressures

Based on REE abundances in megacrysts and host basalts and their equilibrium conditions,it has proved that megacrysts may have been produced from the magma derived from the host rocks or of more basic composition.The REE ratios of megacrysts to host rocks may be taken as partition coefficients when both are equilibrium with each other.The crystal fractionation of megacrysts has caused the evolution of REE in the magma.It is obvious that some host basalts are the product of magma evolution after crystal fractionation.According to REE abundances in the host rocks and the partition coefficients between crystal and liquid,the history of crystal fractionation of magma can be traced.     

海南岛石炭纪双峰式火山岩及其板块构造背景

海南岛西部的石炭纪火山岩为一套大洋拉斑玄武岩-流纹斑岩的双峰式火山岩。玄武岩中的不相容元素和稀土元素的丰度和比值,以及稀土分配模式与大陆裂谷的拉斑玄武岩的地球化学特征一致,说明海南岛晚古生代裂谷作用的存在。玄武质岩浆来源于地幔深部,演化程度较低,受下地壳物质混染。流纹质岩浆不是玄武岩浆结晶分异产物,而是受裂谷区高热流影响,由陆壳部分熔融形成。     

Essexite occurrence in the Deccan volcanic province of Saurashtra,western India

The occurrence of essexite in the Deccan volcanic province of Saurashtra, India, is reported here for the first time. The essexite body occurs as a large stock-like intrusion in horizontal flow basalts. Petrographically it is characterized by the presence of titanaugite, labradorite, olivine, iron oxides and accessory amounts of alkali feldspar, analcite, biotite and apatite. Chemically it is characterized by enrichment in LILE, HFSE and REE as compared to the other tholeiitic and alkaline basalts of the area. It is therefore concluded that the essexite magma has not formed by differentiation out of the tholeiitic magma predominantly encountered in the Deccan volcanic province, but possibly represents a separate melt derived as a 5 to 10% partial melt at shallower depth (15 kb pressure) within the upper mantle.     

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.     

Geochemistry of the Rare Earth elements in spilites from the oceanic and continental crust

Analytical data including major elements, the Rare Earths, Ni, Cu, Zn, Rb, and Sr are presented for twenty-three spilites from the Mid-Atlantic Ridge, the Hercynian part of the Variscan geosyncline in Germany, and several localities in Switzerland. Low grade metamorphism (up to approximately 400° C) and spilitization of basaltic rocks apparently do not alter the original Rare Earth element (REE) distributions. This fact permits comparison of the spilites and unaltered tholeiitic basalts from the Mid-Atlantic Ridge. The relative REE distributions thus appear suitable for delineating the original basalt types of spilites formed by metamorphism. The spilites from the Hercynian part of the Variscan geosyncline have a REE distribution pattern which is characteristic of continental tholeiites. It is thus probable that during the formation of this geosyncline the principal magma extruded was of tholeiitic composition and that these rocks were later converted to spilites by metamorphism.     

The geochemistry of repetitive cyclical volcanism from basalt through rhyolite in the uchi-confederation greenstone belt,canada

Archean volcanic rocks in the Confederation Lake area, northwestern Ontario, Canada, are in three mafic to felsic cycles collectively 8,500 to 11,240 m thick. Each cycle begins with pillowed basalt and andesite flows and is capped with andesitic to rhyolitic pyroclastic rocks and minor flows. Seventy five samples from this succession were analyzed for major and trace elements including the rare earth elements. In two cycles, tholeiitic basalts are overlain by calcalkaline andesite to rhyolite. In the third, cycle, the tholeiitic basalts are overlain by tholeiitic rhyolites. Fe enrichment in basalts is accompanied by depletion of Ca, Al, Cr, Ni, and Sr, and enrichment in Ti, P, the rare earth elements, Nb, Zr, and Y. This is interpreted as open system fractionation of olivine, plagioclase, and clinopyroxene. Si enrichment in dacites and rhyolites is attributed to fractional crystallization of plagioclase, K-feldspar, and biotite. Tholeiitic basalt liquids are believed to be mantle-derived. Intercalated andesites with fractionated rare earth patterns appear to be products of mixing of tholeiitic basalt and rhyolite liquids and, andesites with flat rare earth patterns are probably produced by melting of previously depleted mantle. Felsic magmas are partial melts of tholeiitic basalt or products of liquid immiscibility in a tholeiitic system perhaps involving extreme fractionation in a high level magma chamber, and assimilation of sialic crust. It is concluded that Archean cyclical volcanism in this area involves the interplay of several magmatic liquids in processes of fractional crystallization, magma mixing, liquid immiscibility, and the probable existence of compositionally zoned magma chambers in the late stages of each cycle. The compositionally zoned chambers existed over the time period represented by the upper felsic portion of each cycle.     

汉诺坝玄武岩Re-Os同位素地球化学——Re的挥发性丢失和壳-幔相互作用的证据

本文报道了采自汉诺坝玄武岩区周坝和白龙硐剖面以及白布洛张20井等地29个玄武岩样品的Re、Os含量和~(187)Os/~(188)Os比值。Os含量为11×10~(-12)～314×10~(-12),Re含量为40×10~(-12)～238×10~(-12),Re和Os含量有正相关趋势。碱性玄武岩(AK)的Re、Os含量高于拉斑玄武岩(TH)和过渡玄武岩(TR),玄武岩Os含量变化与分离结晶作用有关,玄武岩的低Re含量与地面喷发的火山岩浆脱气过程中Re的挥发性丢失作用有关。玄武岩的~(187)Os/~(188)Os比值为0.14735～0.61136,AK的~(187)Os/~(188)Os比值比TH和TR低且变化小。玄武岩的~(187)Os/~(188)Os比值与Os含量有负相关性。随着Os含量降低到小于75×10~(-12),~(187)Os/~(188)Os比值迅速升高,反映了地壳混染在TH和TR成因中的贡献。在以往的研究中没有观察到类似的地壳混染作用,说明了Re-Os同位素体系在示踪壳源物质上的优势。一些Os含量较高的TH的~(187)Os/~(188)Os比值表明其地幔源区既非亏损的又非经交代富集的SCLM,可能是混入了地壳俯冲物质的"Marble cake"型地幔。总之,汉诺坝玄武岩的Re-Os同位素地球化学研究支持了以往研究的主要成果,两类玄武岩地球化学差异性和异源成因论;分离结晶和部分熔融过程在玄武岩成因中的重要作用;碱性玄武岩的成因与地幔柱的关系等。同时揭示了一些新的现象:汉诺坝玄武岩形成中存在少量的地壳混染作用;地面喷发的火山熔岩在脱气过程中Re的挥发性丢失;拉斑玄武岩的源区更有可能为"Marble cake"型地幔。