Carbon dioxide in igneous petrogenesis: II. Fluid dynamics of mantle metasomatism

Petrographic, fluid inclusion, geochemical and isotopic evidence from xenoliths in alkali basalts suggests that low-viscosity fluids rich in O-H-C, dissolved silicates and especially the incompatible elements may ascend, decompress and precipitate crystalline phases and/or induce partial fusion in the upper mantle. Such mantle metasomatic fluids (MMF) may be important in generating isotopic heterogeneity and in transporting and focusing mantle heat. In order to model the movement of MMF, the ordinary differential equations governing the variation ofP, T, ascent velocity and fluid density of a compressible, viscous, single-phase (H₂O or CO₂) non-reacting fluid ascending through a vertical crack of constant width have been solved. A large number of numerical simulations were carried out in which the significant factors affecting flow behavior (thermodynamic and transport fluid properties, roughness and width of cracks, geothermal gradient, initial conditions, etc.) were systematically varied. The calculations show that: (1) MMF tends to move at uniform rates following a short period of rapid initial acceleration, (2) MMF ascends nearly isothermally, (3) MMF acts as an efficient heat transfer agent; numerical experiments show that transport of heat into regions undergoing metasomatism can lead to partial fusion. The heat transported by movement of MMF averaged over the age of the Earth is sufficient to generate about 0.1 km³ of basaltic magma per year, which is approximately equal to the production rate of alkaline magma. If an intense period of mantle degassing occured early in the history of the Earth, the transport of heat and mass (K, U, Rb, LREE) by migrating fluids might have been important.     

Cognate clinopyroxene from Paleogene mantle xenolith-bearing basanite lavas (East Serbia, SE Europe): the role of dissolution of mantle orthopyroxene

The study focuses on clinopyroxene from mantle xenolith-bearing East Serbian basanites and suggests that dissolution of mantle orthopyroxene played an important role in at least some stages of the crystallization of these alkaline magmas. Five compositional types of clinopyroxene are distinguished, some of them having different textural forms: megacrysts (Type-A), green/colourless-cored phenocrysts (Type-B), overgrowths and sieve-textured cores (Type-C), rims and matrix clinopyroxene (Type-D), and clinopyroxene from the reaction rims around orthopyroxene xenocrysts (Type-E). Type-A is high-Al diopside that probably crystallized at near-liquidus conditions either directly from the host basanite or from compositionally similar magmas in previous magmatic episodes. Type-B cores show high ^VIAl/^IVAl≥1 and low Mg# of mostly <75 and are interpreted as typical xenocrysts. Type-C, D and E are interpreted as typical cognate clinopyroxene. Type-D has Mg#<78, Al₂O₃?=?6–13?wt.%, TiO₂?=?1.5–4.5?wt.%, and Na₂O?=?0.4–0.8?wt.% and compositionally similar clinopyroxene is calculated by MELTS as a phase in equilibrium with the last 30?% of melt starting from the average host lava composition. Type-C has Mg#?=?72–89, Al₂O₃?=?4.5–9.5?wt.%, TiO₂?=?1–2.5?wt.%, Na₂O?=?0.35–1?wt.% and Cr₂O₃?=?0.1–1.5?wt.%. This clinopyroxene has some compositional similarities to Type-E occurring exclusively around mantle orthopyroxene. Cr/Al vs Al/Ti and Cr/Al vs Na/Ti plots revealed that Type-C clinopyroxene can crystallize from a mixture of the host basanite magma and 2–20?wt.% mantle orthopyroxene. Sieve-textured Type-C crystals show characteristics of experimentally produced skeletal clinopyroxene formed by orthopyroxene dissolution suggesting that crystallization of Type-C was both texturally and compositionally controlled by orthopyroxene breakdown. According to FeO/MgO^cpx/melt modelling the first clinopyroxene precipitating from the host basanite was Type-A (T?~?1250?°C, p?~?1.5?GPa). Dissolution of orthopyroxene produced decreasing FeO/MgO^melt and crystallization of Type-E and sieve-textured Type-C clinopyroxene (0.3–0.8?GPa and 1200–1050?°C). The melt composition gradually shifted towards higher FeO/MgO^melt ratios precipitating more evolved Type-C and Type-D approaching near-solidus conditions (<0.3?GPa; ~950?°C).     

Direct ascent to the surface of asthenospheric magma in a region of convex lithospheric flexure

The stress field of oceanic lithosphere controls the distribution of submarine petit-spot volcanoes. However, the eruption sites of these petit-spot volcanoes are considered to be limited to concavely flexed regions of lithosphere off the outer rise. Here, we present new data for a recently identified petit-spot lava field on a convexly flexed section of the lithosphere adjacent to the subduction zone offshore of northeast Japan in an area containing more than 80 volcanoes. This area is marked by strongly alkaline lavas that were erupted on the convexly flexed region. As for the concavely flexed region where the petit-spots previously reported, the base of the lithosphere beneath the eruption sites is under extension, whereas the upper part of the lithosphere is under compression. This change in the stress field, from the lower to upper lithosphere, causes ascending dikes to stall in the mid-lithosphere, leading to metasomatic interaction with the surrounding peridotite. The new geochemical data of rocks and xenocrysts presented in this study indicate that strongly alkaline magmas erupted on the convexly flexed region would have ascended more rapidly through the mid-depth of lithosphere because of the extensional regime of the upper lithosphere and decreasing the degree of metasomatic reaction with the surrounding mantle peridotite. The results indicate that the degree of metasomatism and the compositional variations of petit-spot magmas are controlled mainly by the stress field of the lithosphere.     

Petrology and evolution of transitional alkaline — sub alkaline lavas from Patmos,Dodecanesos, Greece: evidence for fractional crystallization,magma mixing and assimilation

Petrographic, mineral chemical and whole-rock major oxide data are presented for the lavas of the Main Volcanic Series of Patmos, Dodecanesos, Greece. These lavas were erupted about 7 m.y. ago and range in composition from ne-trachybasalts through hy-trachybasalts and trachyandesites to Q-trachytes. To some extent, the ne-trachybasalts are intermediate in composition to the alkaline lavas found on oceanic islands and the calc-alkaline lavas of destructive plate margins. Major oxide variation is largely explicable in terms of fractional crystallization involving removal of the observed phenocryst and microphenocryst phases viz. olivine, plagioclase, clinopyroxene and Ti-magnetite in the mafic lavas, plagioclase, clinopyroxene, mica and Ti-magnetite in the evolved lavas. Apatite, which occurs as an inclusion in other phenocrysts or as microphenocrysts must also have been removed. However, mass balance calculations indicate that the chemistry of the hy-trachybasalts is inconsistent with an origin via fractional crystallization alone and the complex zoning patterns and resorbtion phenomena shown by phenocrysts in these lavas show that they are hybrids formed by the mixing of 80-77% ne-trachybasalt with 20–23% trachyandesite. It is estimated that the mixing event preceded eruption by a period of 12 h-2 weeks suggesting that mixing triggered eruption. Combined fractionation and mixing cannot explain the relatively low MgO contents of the hy-trachybasalts and it is concluded that assimilation also occurred. Assimilation, and especially addition of volatiles to the magmas, may be responsible for the evolutionary trend from ne-normative to hy-normative magmas and was probably facilitated by intensified convection resulting from mixing. A model is presented whereby primitive magma undergoes fractionation in an intracrustal magma chamber to yield more evolved liquids. Influx of hot primitive magma into the base of the chamber facilitates assimilation, but eventually mixing yields the hy-trachybasalts and finally the ne-trachybasalts are erupted.     

Geochemistry and petrogenesis of sodic and potassic mafic alkaline rocks in the Deccan Volcanic Province, Mumbai Area (India)

Summary Major element, trace element, Sr- and Nd-isotopes and mineral chemical data are reported for alkaline rocks (lamprophyres, tephrites, melanephelinites, nephelinites and nepheline syenites) cross-cutting the Deccan Trap lava flows south (Murud-Janjira area) and north of Mumbai (Bassein). These rocks range from sodic to potassic and have a large span in MgO (12–2 wt%). The lamprophyres have high content of incompatible elements (e.g., TiO₂ > 3.8 wt%, Nb > 130 ppm, Zr > 380 ppm, Ba > 1200 ppm), and relatively high initial (at 65 Ma) ¹⁴³Nd/¹⁴⁴Nd (0.5128) and low ⁸⁷Sr/⁸⁶Sr (0.7038–0.7042). They are likely to be small-degree melts (2–3%) of volatile- and incompatible element-enriched mantle sources, similar to other alkaline rocks in the northern Deccan, though slightly more potassium-rich. The nepheline-rich rocks have highly porphyritic textures (up to 57% phenocrysts of diopside ± olivine), and anomalously low contents of incompatible elements (e.g., TiO₂ < 1.3 wt%, Nb < 24 ppm, Zr < 100 ppm) indicating that they could not represent liquid compositions. Moreover, their very low initial ¹⁴³Nd/¹⁴⁴Nd ratios (0.5116–0.5120), at ⁸⁷Sr/⁸⁶Sr = 0.7045–0.7049, are unusual in the rocks related to the Deccan Traps and identify a new end-member in this province, that could be identified as “Lewisian-type” lower crust and/or enriched mantle. The melting episode that generated these alkaline rocks likely occurred close to the base of the ca. 100 km-thick Indian lithosphere, very shortly after the main eruption of the Deccan tholeiites. Received January 14, 2000; revised version accepted September 28, 2001     

A review of coal properties pertinent to carbon dioxide sequestration in coal seams: with special reference to Victorian brown coals

This paper presents reviews of studies on properties of coal pertinent to carbon dioxide (CO₂) sequestration in coal with specific reference to Victorian brown coals. The coal basins in Victoria, Australia have been identified as one of the largest brown coal resources in the world and so far few studies have been conducted on CO₂ sequestration in this particular type of coals. The feasibility of CO₂ sequestration depends on three main factors: (1) coal mass properties (chemical, physical and microscopic properties), (2) seam permeability, and (3) gas sorption properties of the coal. Firstly, the coal mass properties of Victorian brown coal are presented, and then the general variations of the coal mass properties with rank, for all types of coal, are discussed. Subsequently, coal gas permeability and gas sorption are considered, and the physical factors which affect them are examined. In addition, existing models for coal gas permeability and gas sorption in coal are reviewed and the possibilities of further development of these models are discussed. According to the previous studies, coal mass properties and permeability and gas sorption characteristics of coals are different for different ranks: lignite to medium volatile bituminous coals and medium volatile bituminous to anthracite coals. This is important for the development of mathematical models for gas permeability and sorption behavior. Furthermore, the models have to take into account volume effect which can be significant under high pressure and temperature conditions. Also, the viscosity and density of supercritical CO₂ close to the critical point can undergo large and rapid changes. To date, few studies have been conducted on CO₂ sequestration in Victorian brown coal, and for all types of coal, very few studies have been conducted on CO₂ sequestration under high pressure and temperature conditions.     

Estimation of the Primary Magma Compositions of an Igneous Rock Series Petrogenetically Associated with Fractional Crystallization with Special Reference to Element Abundance Relationships

A primary magma not only represents the starting point of a fractional crystallization process, but also is the product of an equilibrium or fractional partial melting process in a mantle.Element abundance relationships in the primary magma obey both law of power function for fractional crystallization and the law of fractional linear function for equilibrium partial melting .Based on this double nature of the primary magma, the authors advanced a principle to restore the primary magma composition from that of an igneous rock series with petrogenesis of fractional crystallization and put forward an approach of estimating the element abundance of the primary magma, exempli-fied by the rar-earth elements in the Andes volcanic rock series.     

幔源岩浆持续提供热的有力证据：以湘南九嶷山花岗岩体中暗色包体成因研究为例

湘南九嶷山复式花岗岩体位于南岭西段, 由一个加里东期岩体和四个燕山期岩体组成。其西侧金鸡岭岩体中广泛发育形态多样的暗色包体。本次选取一个2m×2.5m不规则椭球形包体开展研究, 发现它与寄主岩具有较为相近的年龄、矿物组合、地球化学和同位素特征: (1)SIMS锆石U-Pb定年结果显示寄主岩和暗色包体的年龄分别为154.0±1.6Ma和151.4±2.1Ma, 两者在误差范围内一致; (2)两者均以钾长石、石英、斜长石、黑云母、磷灰石、锆石等为主要的矿物组成, 但在矿物组成比例、粒度和形态上有所差距; (3)寄主岩和暗色包体的SiO₂含量分别为70.9%~75.6%和67.3%~68.0%, 两者均富集大离子亲石元素(LILE)而亏损高场强元素(HFSE), 但暗色包体的LILE略低于寄主岩而HFSE略高于寄主岩; (4)寄主岩的ε_Hf(t)值和δ¹⁸O值分别为-8.6~-0.4和7.8‰~8.9‰, 包体的ε_Hf(t)值和δ¹⁸O值分别为-7.0~+1.6和7.3‰~8.9‰。这些特征表明, 金鸡岭暗色包体是由富钾的下地壳玄武质变质火成岩在受到幔源岩浆持续加热后发生部分熔融, 熔融产物注入到已存在于中上地壳的岩浆房中(寄主岩)后发生淬冷作用形成的。尽管寄主岩和暗色包体均是下地壳物质发生部分熔融的产物, 但地壳成分的不均一性导致两者拥有略有差异的同位素和元素组成。沿南岭郴州-临武北东走向断裂带从南向北依次分布有姑婆山、铜山岭、九峰、骑田岭、宝山、锡田花岗质岩体, 其所含暗色包体的ε_Hf(t)和δ¹⁸O值从亏损(+8、5‰)到富集(-8、9‰)变化范围很大, 表明南岭地区暗色包体成因模式具有多样性, 但无论是哪种类型, 幔源岩浆的长期活动持续为下地壳的熔融和岩浆房演化提供热量是一个必不可少的重要因素。

     

Geochemistry of the mafic dykes in parts of the Singhbhum granitoid complex: petrogenesis and tectonic setting

Singhbhum granitoid complex has been intruded by numerous mafic dykes trending in different directions. The studied dykes were originated from subalkaline magma, ranging in composition from basalt through basaltic-andesite to andesite. In the present work, the studied dykes are divided into two groups on the bases of abundance of SiO₂, MgO, Al₂O₃, Ni, and Cr. The first one has higher Mg# than that of group II. These dykes have enriched incompatible trace element patterns. These are particularly enriched in the light rare earth elements and large ion lithophile elements with depleted high field strength elements (Nb, P, Ti). High Ba/Nb and Sr/P ratios of present mafic dykes are the indications of subduction signature. The geochemical characters of the back arc extension basalt tectonic setting is suggested for the studied dykes. Higher PM-normalized Th/Nb, Rb/Nb, and Ba/Nb ratios of studied samples support their non-plume source.     

Conditions of ore mineral formation in certain Zambian Copperbelt deposits with special reference to the role of cobalt

Studies of the compositions of coexisting sulphide assemblages from certain Zambian Copperbelt deposits and of their textural relations and host rock environments have been undertaken by routine microscopy and using electron microprobe analysis. Special attention has been paid to sulphide assemblages containing cobalt. Using experimental data on the systems Cu-Co-S, Cu-Fe-Co-S and on sulphidation equilibria, together with the available information on equilibria involving gangue minerals and some new calculations, an attempt has been made to define the chemical conditions of ore formation and/or re-equilibration in several deposits (Baluba, Chibuluma West and Chibuluma, Chambeshi S.E.). If a re-equilibration temperature of 300°C is assumed the range of aS₂ prevailing during final formation of the assemblages was of the order 10^–7 – 10^–9 atm, more rarely dropping to 10^–11 – 10^–12 atm. If magnetite is present, and this is considered very unlikely in most cases, aO₂ may have reached as high as 10^–35 atm but it is generally likely to have been around 10^–50 atm or even lower. Values of aCO₂ are assumed to have been of the order of 10^–0.5 atm. Detailed studies of drill hole samples from the Chambeshi S.E. deposit suggest an important link between the petrology of the host rocks and the sulphide mineral chemistry. In particular, the control exerted on sulphide composition by aS₂ may have been related to the availability of sulphate in the form of diagenetic anhydrite or in sulphate-rich interstitial waters. The distinctive distribution of cobalt in the ores appears related to the distribution of amphibolite bodies and in turn to rift fault systems in the Basement which allowed upward movement of fluids enriched in magmatically derived cobalt.     

The role of fluorine in submarine exhalative systems with special reference to Broken Hill,Australia

Fluorine-bearing minerals are uncommon in submarine exhalative ores, exhalites and associated alteration zones, probably because of the low solubility of CaF₂. The Broken Hill (Australia) deposit contains fluorapatite and fluorite with one lens containing 1.35% F and greater than 3 volume % F-bearing minerals. The calcite-fluorite-fluorapatite assemblage at Broken Hill indicates that ore deposition was probably from hypersaline fluorine-bearing fluids which decreased in pH by base leaching reactions which released Ca²⁺ and mixing with seawater promoting the rapid and simultaneous precipitation of calcite, fluorite and fluorapatite as a result of temperature and salinity decrease and pH and [Ca²⁺] increase. The abundance of fluorine minerals in the Broken Hill ore and the association of F and B minerals with stratigraphically equivalent W- and Sn-bearing exhalites suggest that F complexes are important for ore transport in some exhalative systems. The Fe/Mn ratio decreases and the F/Cl ratio increases in fluorapatite in exhalites with increasing proximity to the Broken Hill deposit.     

The role in lateritic nickel mining in Latin American countries with special reference to exmibal in Guatemala

Modern mining operations can result in significant economic development within the developing host countries. Lateritic nickel mining plays a role of varying importance in a number of Latin American countries, depending on natural resource endowments and government policies. Exploraciones y Explotaciones Mineras Izabal, SA (Exmibal) is a large-scale lateritic nickel mining operation that serves as an excellent case study in the analysis of mining-induced economic development at local, regional and national scales. Exmibal's turbulent history demonstrates the need to view mining dynamically and in the context of production and consumption restraints. Guatemala's experience will Exmibal may be generalized most successfully to other Latin American countries that have or may have one large nickel mining complex operated by a transnational enterprise.     

Double injection events of mafic magma into supersolidus Yucheon granites to produce two types of mafic enclaves in the Cretaceous Gyeongsang Basin,SE Korea

Petrographic and geochemical features of the Cretaceous Yucheon granites and their mafic microgranular/magmatic enclaves (MMEs), SE Korea, reveal that the MMEs originated from magma mixing. Mesoscopic and microscopic features indicate that mechanical mixing operated heterogeneously to produce the MMEs with a wide range of sizes and textures. Chemical compositions of amphibole, biotite, and plagioclase rims of both the MMEs and host granites are almost identical, indicating that chemical homogenization took place to some extent after the mechanical mixing. Plagioclase cores, however, have various compositions depending on the host rocks and/or sampling locations, suggesting their sluggish re-equilibration. The MMEs are divided into Type A (low TiO₂, very fine-grained, chilled margins) and Type B (high TiO₂, fine- to medium-grained, no chilled margins). The lower TiO₂ MMEs cooled more rapidly and interacted with granitic magma for a shorter period of time than the higher TiO₂ MMEs. Additionally, the former are less enriched in HREEs than the latter. Zoned plagioclase has two zones of increased An content. These features are indicative of double injection events of mafic magma. A previous model explains the magma mixing as resulting from the generation of a slab window due to Kula-Pacific ridge subduction. The model cannot, however, explain the eastward younging of the granites in Korea, necessitating a new, more elaborate model of Cretaceous geodynamics and magmatism in East Asia.     

Aid to refugees — shortcomings: with special reference to eastern Sudan

An attempt is made to review shortcomings in refugee and displaced people aid and rehabilitation in eastern Sudan. Shortcomings are discussed as related to the recipients, the local inhabitants and the environment. Contributing factors are evaluated and an alternative approach is recommended. Environmental conservation being the focus, trust and coordination are the means.     

Urbanization and desertification in the Sudan with special reference to Khartoum

Urbanization-desertification interactions in the arid zones of the Sudan represent a challenge for future management planners. Desertification leads to a considerable movement into the towns, thereby encouraging the urbanization process. However, due to the large pull effect of large urban centres which are limited in number and unevenly distributed over the area, most of the migration is oriented towards them. This tendency is strengthened, furthermore, by the present planning trends of growth pole centres. The result is overcrowding, negative over-urbanization diseconomies and more pressure on the natural resources in the immediate hinterland, thus further accelerating the desertification process. Some examples are given in the paper to show how the rapid increase of urban population and the rapid growth of urban centres have reflected themselves in difficulties in procuring wood fuel or naturally grown raw materials for traditional and small urban industries. The specific example of Khartoum, the largest urban centre in the Sudan with the highest rate of growth is treated in detail to show how rapid urbanization processes would result in intensified desert conditions and how ecological interactions and effects would be faster and more serious in a more vulnerable ecological location.     

Indian MORB-type mantle beneath the Kuril Island arc: Isotopic investigation of the mafic lavas of Kunashir Island

New data on the Hf, Pb, and Nd isotopes of the mafic rocks of various ages from Kunashir Island were used to address the nature of the sub-arc mantle of the southern segment of the Kuril island arc. At least since Late Cenozoic, its isotopic characteristics have been the MORB-type mantle of the Indian Ocean. Its boundary with the mantle reservoir of the Pacific MORB-type coincided probably with the Kuril-Kamchatka Trench.     

Origin of rhyolite and rhyodacite lavas and associated mafic inclusions of Cape Akrotiri,Santorini: the role of wet basalt in generating calcalkaline silicic magmas

Amphibole-bearing mafic inclusions (low to medium-K high-alumina basalt to basaltic andesite) comprise 4.1 vol% of calc-alkaline rhyolite and rhyodacite lavas on Akrotiri Peninsula, Santorini, Greece. Physical features indicate a magmatic origin for the inclusions, involving mingling with the host silicic magma and quenching. Water contents of the mafic magmas are estimated to have been above 4% at water pressures of 1.8 kbars or more at temperatures of approximately 950–1,000 °C. Three evolutionary stages are inferred in their petrogenesis. In the first stage infiltration of slab fluids promotes partial melting in the mantle to generate primitive wet basaltic magmas enriched in LREE, LILE, Th and U in comparison to N-type MORB. In the second stage storage and crystal differentiation of primitive magmas occurred in the lithospheric mantle or deep crust, involving olivine, spinel and clinopyroxene followed by amphibole and plagioclase. In the third stage differentiated mafic magma intrudes into porphyritic silicic magma at shallower crustal levels (estimated at 7–10 km). Mingling and quenching of the mafic magmas within the silicic host causes chemical or physical interactions between the inclusions and the host prior to and during eruption. The silicic lavas have geochemical affinities with the mafic inclusions, but are relatively depleted in MREE, HREE and Y and enriched in Rb relative to Ba and K. These observations are consistent with involvement of amphibole in magma genesis due either to crystal differentiation from wet basalt or to partial melting of mafic rocks with residual amphibole. Crystallization of wet basalt in the deep crust is preferred on the basis of physical considerations.Electronic Supplementary Material Supplementary material is available for this article if you access the article at . A link in the frame on the left on that page takes you directly to the supplementary material.Editorial responsibility: I. Parsons     

Problems of agriculture in Slovenia with special reference to Cirkovce

The transition in the Slovenian countryside is examined through a case study of Cirkovce, a local centre for the central southern section of the Dravsko polje plain where natural and socio-geographical factors underpin a mixed rural-urban structure. Farming is intensive, but a high percentage of people are now employed outside agriculture; a situation which is reflected clearly in the appearance of the settlement. The process of rural depopulation, balanced by the growth of employment in industry and services, is reflected in a secondary knot of settlement around Cirkovce's railway station. Agriculture is still very significant but there needs to be some consolidation of landholding to create larger units suitable for market production and food processing. But the village must also improve its range of functions and provide a better environment for the non-agricultural population which will become increasing important for its future development. This revised version was published online in July 2006 with corrections to the Cover Date.     

大同新生代火山岩浆的快速喷发——来自橄榄石地幔捕掳晶的证据

量化研究幔源岩浆从源区运移至喷发或者侵位的时间尺度，对理解基性岩浆作用具有重要意义。然而，对于岩浆的喷发和就位的时间尺度研究仍缺乏有效的约束，位于我国华北克拉通北部山西大同新生代火山岩群是理想的研究地区。本文以该火山群～0.2 Ma喷发的神泉寺碱性玄武岩为研究对象，重点研究其中携带的地幔橄榄石捕掳晶来约束喷发前的时间尺度。通过对其开展详细的矿物化学研究，发现地幔捕掳晶核部的Fo值高达97.7,为极富镁橄榄石，结合其极低的Ca、Mn和Ni含量特征，认为它们捕获自被交代的地幔橄榄岩。另外，地幔橄榄石捕掳晶发育明显的CaO成分环带，表明其在地壳岩浆系统内经历了复杂的岩浆演化过程。地幔橄榄石捕掳晶反应边宽度变化很大，说明它们在源区被捕获时及在运移过程中经过了多次破碎过程。橄榄石捕掳晶最边缘的Fo值为70左右，平衡计算表明它们在边部已与主岩浆(碱性玄武岩)达到平衡。Fe-Mg元素扩散计时结果显示，橄榄石地幔捕掳晶仅在岩浆中滞留了几个月的时间。对于40～70 km的岩石圈地幔厚度来说，岩浆平均上升速率最快可能超过500 m/d。     

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.