Particularités de la contamination crustale des phonolites : exemple du Velay oriental (Massif central)

Sr and Nd isotopic compositions of one trachyte, eight phonolites and five basalts have been measured. The isotopic characteristics of the trachyte can be explained by a combined assimilation–fractional crystallization process within an upper crustal magmatic chamber. Some phonolites display isotopic signatures identical to basalts, suggesting that they have been protected against any crustal assimilation during their formation. Some others have low Sr contents, whereas they are enriched in radiogenic Sr (0.70451<⁸⁷Sr/⁸⁶Sr_i<0.71192), and display basaltic ¹⁴³Nd/¹⁴⁴Nd ratios. Both observations could be explained by very strong alkali feldspar fractionation and by subsequent very low assimilation of surrounding rocks (between 0.3 and 4%) during intrusion. To cite this article: J.-M. Dautria et al., C. R. Geoscience 336 (2004).     

Compositional variations (major and trace elements) of clinopyroxene and Ti-andradite from pyroxenite, ijolite and nepheline syenite, Alnö Island, Sweden

Clinopyroxenes from pyroxenite, ijolite and nepheline syenite from the main intrusion of the Alnö complex define two sub-parallel compositional trends with respect to Na, Ca and Fe_TOT plotted against alkali-pyroxene fractionation index (Na–Mg). Both trends define a smooth fractionation of increasing Na and Fe_TOT and decreasing Ca with increasing Na–Mg, but one set of samples contain clinopyroxenes that constantly plot at higher Na and lower Fe_TOT and Ca (at similar Na–Mg) than the rest of the samples. Clinopyroxenes with higher Ca and Fe_TOT and lower Na (trend 1) co-exist with substantial amounts of Ti-andradite (up to 70 vol.%), while the sample set defining the more Na-rich trend (trend 2) lack co-existing Ti-andradite. Clinopyroxenes from both trends show fractionated REE patterns with a distinct difference in HREE content, reflecting the content of co-existing Ti-andradite. The rocks of the first Ti-andradite-bearing trend crystallized slightly prior to the rocks of the second trend, probably from a primitive, Ca- and Ti-rich nephelinitic magma. Crystallisation of pyroxenite and melteigite occurred under low aSiO₂ and high aCaO and aTiO₂ as evidenced by the presence of perovskite and sometimes substantial amounts of magnetite. Subsequent increase in aSiO₂ is evidenced in the overgrowth of perovskite by titanite, which in turn is overgrown by Ti-andradite. Nepheline syenitic residuals crystallized under higher aSiO₂ and aNa₂O and lower aCaO and aTiO₂, which reduced Ti-andradite into an accessory phase and produced more Si- and Na-rich clinopyroxenes. Some of these residuals probably also mixed with new primitive magma producing a hybrid magma that crystallised the more Na-rich and Ca- and Fe_TOT-poor clinopyroxenes of trend 2. The complete lack of Ti-andradite in these rocks indicates different crystallisation conditions and also a different magma composition.     

Origin of Exceptionally Abundant Phonolites on Ua Pou Island (Marquesas, French Polynesia): Partial Melting of Basanites Followed by Crustal Contamination

On the basis of the first systematic mapping of Ua Pou, longknown for its exceptionally abundant phonolites, we estimatethat these rocks cover 65% of the surface of the island whereasmafic lavas cover 27% and intermediate ones 8%. The silica-undersaturatedsuite was erupted in a restricted time span (2·9–2·35Myr), following the emplacement of tholeiites derived from ayoung HIMU-type source at c. 4 Ma. Primitive basanites, derivedfrom a heterogeneous mantle source with a dominant EM II + HIMUsignature, represent likely parental magmas. The series is characterizedby a Daly gap defined by a lack of phonotephrites. We considerthat the most likely model for the origin of evolved lavas ispartial melting at depth of primitive basanites, leaving anamphibole-rich residuum and producing tephriphonolitic magmas.These tephriphonolitic magmas may have evolved by closed-systemfractional crystallization towards Group A phonolites. Threeother groups of phonolites could have been derived from tephriphonoliticmagmas by open-system fractional crystallization processes,characterized respectively by seawater contamination (GroupB), assimilation of nepheline syenite-type materials (GroupC) and extreme fractionation coupled with assimilation of theunderlying oceanic crust (Group D). The prominence of evolvedlavas is a consequence of their origin from partial meltingof mafic precursors followed by crustal contamination. KEY WORDS: Marquesas; French Polynesia; phonolite; partial melting; contamination     

Petrology,geochemistry and geodynamic setting of Eocene-Oligocene alkaline intrusions from the Alborz-Azerbaijan magmatic belt,NW Iran

The Kaleybar, Razgah and Bozqush (KRB) intrusions were studied to better understand subduction-related Eocene-Oligocene alkaline magmatism in NW Iran. The bulk of intrusions mainly consist of Si-undersaturated rocks including foid-bearing monzonite and syenite (nepheline syenite, pseudoleucite syenite) with some foid-bearing diorite and gabbro. In addition, they are spatially associated with Si-saturated rocks ranging in composition from monzo-diorite to syeno-granite. The main mafic rock-forming minerals of the studied rocks are olivine (Fo₄₄Fa₅₆), clinopyroxene (diopside to augite), biotite (Mg-biotite through Fe-biotite), amphibole (ferro-pargasite and magnesio-hastingsite with Mg#<0.55), and garnet (Ti-andradites). Based on whole rock geochemistry, the foid-syenites and associated rocks show mildly alkaline (shoshonitic) affinity. The content of SiO₂, K₂O?+?Na₂O, and K₂O/Na₂O ratio ranges from 47.8 to 60.7?wt.%, 5.31 to 16.33?wt.%, and 0.6 to 3.2, respectively. The intrusions are commonly metaluminous, with an aluminum-saturation index (ASI) ranging from 0.66 to 1.01. Almost all the rocks display similar arc-related geochemical features characterized by the enrichment in large ion lithophile elements (LILE) and light rare earth elements (LREE) together with the depletion in high field strength elements (HFSE). The chondrite-normalized REE patterns show no to marked negative Eu anomaly (Eu/Eu*?=?0.55 to 1.12), (La/Yb)_N?=?8.16 to 31, (La/Sm)_N?=?2.80 to 10.59, and (Tb/Yb)_N?=?0.84 to 2.40. The evaluation of the REE patterns for the KRB magmas and the comparison of the trace element ratios with experimental studies indicate a chemically enriched lithospheric mantle source composed of garnet-spinel-lherzolite that have underwent a low degree of partial melting <5% to generate the KRB intrusions. Based on the present data, we infer that the mantle source was contaminated by a subduction component and the melting of the mantle lithosphere occurred by local extension in an overall convergent regime in NW Iran. The extension regime during the Eocene is proposed to be the result of the Neo-Tethys slab roll-back and the Sevan-Akera-Qaradagh (SAQ) slab break-off.     

Equilibrium and disequilibrium degassing of a phonolitic melt (Vesuvius AD 79 “white pumice”) simulated by decompression experiments

Equilibrium and disequilibrium degassing of a volatile phase from a magma of K-phonolitic composition was investigated to assess its behavior upon ascent. Decompression experiments were conducted in Ar-pressurized externally heated pressure vessels at superliquidus temperature (1050 °C), in the pressure range 10–200 MPa using pure water as fluid phase. All experiments were equilibrated at 200 MPa and then decompressed to lower pressures with rates varying from 0.0028 to 4.8 MPa/s. Isobaric saturation experiments were performed at the same temperature and at 900–950 °C to determine the equilibrium water solubility in the pressure range 30–250 MPa. The glasses obtained from decompression experiments were analyzed for their dissolved water content, vesicularity and bubble size distribution. All decompressed samples presented a first event of bubble nucleation at the capsule–melt interface. Homogeneous bubble nucleation in the melt only occurred in fast-decompressed experiments (4.8 and 1.7 MPa/s), for ΔP ≅ 100 MPa. For these decompression rates high water over-saturations were maintained until a rapid exsolution was triggered at ΔP > 150 MPa. For slower rates (0.0028, 0.024, 0.17 MPa/s) the degassing of the melt took place by diffusive growth of the bubbles nucleating at the capsule–melt interface. This process sensibly reduced water over-saturation in the melt, preventing homogeneous nucleation to occur. For decompression rates of 0.024 and 0.17 MPa/s low water over-saturations were attained in the melt, gradually declining toward equilibrium concentrations at low pressures. A near-equilibrium degassing path was observed for a decompression rate of 0.0028 MPa/s. Experimental data combined with natural pumice textures suggest that both homogeneous and heterogeneous bubble nucleations occurred in the phonolitic magma during the AD 79 Vesuvius plinian event. Homogeneous bubble nucleation probably occurred at a depth of ∼ 3 km, in response to a fast decompression of the magma during the ascent.     

粤中早白垩世亚髻山正长质杂岩体的成分分异及岩石成因

华南的碱性岩浆往往以小岩株形式侵位于早期花岗岩中,指示了伸展拉张的大地构造背景。本文通过对华南代表性的碱性岩体——粤中亚髻山正长质杂岩体不同相带岩石的研究,发现它们可按照岩性和成分的差异划分三组,其成因与岩浆过程和岩浆期后流体作用密切相关。化学成分上,三组的差异体现在:1)Group 1显示最低的Si O2(59.37%~64.10%)、K2O/Na2O(0.70~1.11)、I Sr值(0.70741~0.710032)、t2DM模式年龄(1.0~1.1Ga),最高的Al2O3(17.30%~19.18%)、全碱(K2O+Na2O:11.13%~13.76%)、εNd(t)值(-1.6~-0.9)和碱性-过碱性、准铝质特征;稀土配分曲线呈明显右倾,在原始地幔标准化蛛网图上,表现出Ba、Ti、Sr和P负异常;具有球粒陨石质Nb/Ta比值(平均为19.6)和超球粒陨石值Zr/Hf比值(平均为47.1);2)Group 2显示最高的Ti O2(0.47%~0.49%)、Mg O(0.98%~1.07%)、P2O5(0.15%~0.16%)、K2O/Na2O(2.57~6.69)和中等低的I Sr(0.70845)、εNd(t)值(-7.9~-7.8),具有强过铝质且碱性-钙碱性过渡的特征;稀土配分曲线呈明显右倾,在原始地幔标准化蛛网图上,表现出Nb-Ta、LREE、P和Ti负异常;其Nb/Ta和Zr/Hf比值均近似于平均陆壳(平均值分别为11.6和36.3);3)Group 3具有最低的镁铁质含量、Al2O3(13.00%~13.16%)、εNd(t)值(-8.3)和最高的Si O2(77.50%~76.54%)、I Sr(0.72563)以及与过渡带相似的t2DM模式年龄(1.6Ga),总体显示碱性、强过铝质的特征;稀土配分曲线近似于"海鸥形",Eu异常明显,在原始地幔标准化蛛网图上,显示Ba、Nb、LREE、Sr、P、Ti负异常和Rb、Th、U、Ta、Pb正异常。其Nb/Ta和Zr/Hf比值均远低于平均陆壳(平均值分别为3.0和18.5)。Group 3中锆石的LA-ICP-MS U-Pb定年获得了2个加权平均年龄,即140.9±1.4Ma(MSWD=2.0)和141.4±0.9Ma(MSWD=1.6),与之前报道的Group 1的形成时代一致,表明它们都是早白垩世同一次岩浆作用的产物。这些成分的差异也体现在岩石成因类型判别上,结果显示Group 1属于A型岩套中典型的A1型亚类,而Group 2和Group 3显示似是而非的类型,比如,Group 2具有A型向I型过渡的特征,Group 3则既具有高演化花岗岩的特征,又类似于铝质A型花岗岩。基于Sr-Nd同位素和主、微量元素成分特征,我们认为亚髻山正长质杂岩体中的Group 1形成自富集的上地幔分异的硅不饱和碱性岩浆,较少陆壳物质混染;Group 2岩石则是硅不饱和碱性岩浆在侵位过程中大比例同化混染了外围的佛冈花岗岩而成;而Group 3岩石则是Group 2岩浆发生长石、钛铁矿、磷灰石等矿物分离结晶后再与富氟流体发生显著的相互作用而形成。因此,杂岩体各组岩石成分的明显差异,是碱性岩浆与围岩同化混染及后期流体改造、分异的结果。这进一步暗示诸多似是而非岩石类型的花岗岩,其岩浆过程及其后的流体交代对于其源区岩浆的地球化学特征的影响不容忽视;而这些过程很可能对于一些碱性火成岩及中酸性岩岩体的成分环带的形成及成矿作用具有至关重要的意义。     

Rigid Unit Modes in disordered nepheline: a study of a displacive incommensurate phase transition

 Calculations of the Rigid Unit Modes (RUMs) allowed in the nepheline structure are used to explain the diffuse scattering previously seen in electron diffraction experiments. The RUM calculations also show that the modulation wavelength for incommensurate nephelines is essentially determined by the framework topology. X-ray diffraction is used to measure the intensity of the diffuse scattering as a function of temperature. The diffuse intensity increases sharply at 308 K. This effect is interpreted as being due to the softening of a phonon mode, indicating a phase transition. Measurements of this phase transition below the transition temperature are made using hard mode infrared spectroscopy. Received: 17 February 1999 / Revised, accepted. 15 October 1999     

Crust-mantle interaction in the evolution of the Ilímaussaq Complex, South Greenland: Nd isotopic studies

Sm-Nd isotopic compositions were determined for the peralkaline Ilímaussaq Complex of the Gardar Province of southern Greenland. The majority of the samples in the agpaitic and augite syenitic units have near chondritic initial _Nd(≈ 0), whereas a few samples trend towards _Nd values as low as − 6 at the time of intrusion (1143 Ma). This latter value, from a sample taken from the margin of the complex, lying on the evolutionary trend for Ketilidian country-rock granitoids, suggests that large-scale contamination took place only at the margins of the complex. The similarity of the Nd isotopic compositions of the augite syenite and agpaitic units suggests that their parental magmas were derived from the same reservoir. A comparison of the Nd with existing Sr and Hf isotopic data for the complex suggests an origin by combined assimilation fractionation processes. Assimilation-fractional crystallization modeling of the isotopic compositions indicates that the Ilímaussaq magmas could have formed through fractional crystallization of a basaltic melt while assimilating granitic crust. The model requires initially higher assimilation rates from basalt to augite syenite composition with subsequent decreasing assimilation rates from augite syenite to agpaitic compositions. Alkali granites, which formed after the intrusion of the augite syenites, have isotopic compositions intermediate between those of the augite syenites and the surrounding Ketilidian basement. This implies even greater amounts of assimilation and is interpreted as evidence for an origin through fractionation of a basaltic or augite syenite magma with concurrent assimilation of Ketilidian crust.     

Preliminary phase equilibria of the nepheline-diopside system under variable pressures (up to 28 kb) and temperatures

The nepheline-diopside join defines the ultra-alkaline portion of the basalt tetrahedron and the bulk composition of nephelinitic rocks lie in this join. Schairer and others established that under atmospheric pressure, the join cuts through the primary phase volumes of olivine_ss, carnegieite_ss and nepheline_ss. Melilite coexists with nepheline_ss, olivine_ss and diopside_ss below 1160±10°C and olivine reacts out at low temperature. Experimental studies on seven compositions show the presence of a pseudoeutectic at Ne₇₀Di₃₀ and 1420°C, where diopside_ss, nepheline_ss and liquid are in equilibrium. Olivine and melilite do not appear in the system and the assemblage below 1225±20°C is diopside_ss+nepheline_ss.     

Ion migration in nepheline: a dielectric spectroscopy and computer modelling study

 Using a combination of dielectric spectroscopy and atomistic computer simulation techniques, the dynamical behaviour of the loosely bound (Na⁺ and K⁺) channel ions in nepheline has been investigated. The low-frequency dielectric properties of a natural Bancroft nepheline have been studied from room temperature to 1100 K. At each temperature, the dielectric constant, conductivity and dielectric loss were determined over a range of frequencies from 100 Hz to 10 MHz. At high temperatures a distinct Debye-type relaxation in the dielectric loss spectrum was observed; the activation energy for this process was determined to be 1.38 ± 0.02 eV. Atomistic simulation techniques were used to elucidate the mechanism and energetics of cation migration. A mechanism involving the hopping of Na⁺ ions between oval sites and partially occupied hexagonal (K⁺) sites, via a bottleneck consisting of a distorted sixfold ring of (Al,Si)O₄ tetrahedra, was found to give a calculated energy barrier in very good agreement with the experimentally determined activation energy. These results confirm the nature of the process responsible for the observed dielectric behaviour. Overall, this study demonstrates the intrinsic, microscopic control of cation diffusion processes in rock-forming minerals. Identifying specific energy barriers and preferred diffusion pathways is fundamental to the prediction of diffusion energetics. Received: 8 May 2000 / Accepted: 21 July 2000