New evidence of mantle heterogeneity beneath the Hyblean Plateau (southeast Sicily,Italy) as inferred from noble gases and geochemistry of ultramafic xenoliths

We analyzed major and trace elements, Sr and Nd isotopes in ultramafic xenoliths in Miocenic age Hyblean diatremes, along with noble gases of CO₂-rich fluid inclusions hosted in the same products. The xenoliths consist of peridotites and pyroxenites, which are considered to be derived from the upper mantle. Although the mineral assemblage of peridotites and their whole-rock abundance of major elements (e.g., Al₂O₃ = 0.8–1.5 wt.%, TiO₂ = 0.03–0.08 wt.%) suggest a residual character of the mantle, a moderate enrichment in some incompatible elements (e.g., La_N/Yb_N = 9–14) highlights the presence of cryptic metasomatic events. In this context a deep silicate liquid is considered the metasomatizing agent, which is consistent with the occurrence of pyroxenites as veins in peridotites. Both the Zr/Nb and ¹⁴³Nd/¹⁴⁴Nd ratios of the investigated samples reveal two distinct compositional groups: (1) peridotites with Zr/Nb ≈ 4 and ¹⁴³Nd/¹⁴⁴Nd ≈ 0.5129, and (2) pyroxenites with Zr/Nb ≈ 20 and ¹⁴³Nd/¹⁴⁴Nd ≈ 0.5130. The results of noble-gas analyses also highlight the difference between the peridotite and pyroxenite domains. Indeed, the ³He/⁴He and ⁴He/⁴⁰Ar* ratios measured in the fluid inclusions of peridotites (respectively 7.0–7.4 ± 0.1 Ra and 0.5–8.2, where Ra is the atmospheric ³He/⁴He ratio of 1.38 × 10^? 6) were on average lower than those for the pyroxenites (respectively 7.2–7.6 Ra and 0.62–15). This mantle heterogeneity is interpreted as resulting from a mixing between two end-members: (1) a peridotitic layer with ³He/⁴He ≈ 7 Ra and ⁴He/⁴⁰Ar* ≈ 0.4, which is lower than the typical mantle ratio (~ 1–4) probably due to melt extraction events, and (2) metasomatizing mafic silicate melts that gave rise to pyroxenites characterized by ³He/⁴He ≈ 7.6 Ra, with a variable ⁴He/⁴⁰Ar* due to degassing processes connected with the ascent of magma at different levels in the peridotite wall rock. The complete geochemical data set also suggests two distinct mantle sources for the xenolithic groups highlighted above: (1) a HIMU (high-μ)-type source for the peridotites and (2) a DM (depleted mantle)-type source for the pyroxenites.     

Garnet-spinel-pyroxenite xenoliths from hyblean plateau (South-eastern Sicily, Italy)

Summary Rare garnet-spinel pyroxenite xenoliths occur in some basaltic tuff-breccia levels of Miocene age from the Valle Guffari (Hyblean Plateau, Sicily), together with a number of spinel-bearing mantle xenoliths. The garnet-bearing pyroxenites may be divided into two groups (a and b) on textural and mineralogical bases. Garnet-bearing spinel websterites with a fully recrystallized texture represent the first group (a). Here the garnet (Py_54.5 A1m₃₂ Gr_13.5), with a diffuse kelyphitic alteration, forms a reaction corona between coarse spinel grains and the in contact pyroxenes. The transition from the spinel-pyroxenite to the garnet-pyroxenite field may depend on isobaric cooling from higher (magmatic?) temperatures. Garnet-pyroxene geothermometry indicates that the last equilibration most probably occurred at P = 1.0 GPa (ca.), T = 750 °C (ca).The second lithotype (b) is an orthopyroxene-bearing garnet-spinel clinopyroxenite, exhibiting a complex texture. It consists of zones of coarse clinopyroxene grains enclosing euhedral spinel passing to zones where tiny rounded crystals of the same pyroxene and spinel are enclosed in relatively large patches of extensively kelyphitisized garnet (Py_64.8 Alm_25.6 Gr_9.6). Garnet also occurs as inclusion-free grains up to 4 mm in diameter. P-T calculations give significantly higher values than for the former case (a). The origin of the b-type garnet may also depend on subsolidus reaction of spinel and pyroxenes after an isobaric cooling from still higher temperatures, but a primary magrnatic origin might also be possible, especially for the granular garnets.P-T estimates for both the pyroxenite types closely match a steady geotherm for 100 mW/m² surface heat flow. Such a relatively intense heat flow may suggest the occurrence of huge masses of hot magma intruding the Hyblean lithospheric mantle and lower crust at different levels.

---

Granat-Spinell-Pyroxenit-Xenolithe aus dem Iblei-Plateau (Südost-Sizilien, Italien)

Zusammenfassung Seltene Granat-Spinell-Pyroxenit-Xenolithe kommen in einigen basaltischen Tuff-Breckzien Horizonten miozänen Alters aus dem Valle Guffari (lblei-Plateau, Sizilien) zusammen mit einer Anzahl von Spinell-führenden Mantel-Xenolithen vor. Aufgrund textureller und mineralogischer Kriterien können die Granat-führenden Pyroxenite in zwei Gruppen (a und b) unterteilt werden. Granat-führende Spinell-Websterite mit vollkommen rekristallisierter Textur repräsentieren die erste Gruppe (a). Hier bildet Granat (Py_54.5 Alm₃₂ Gr_13.5) mit einer diffusen kelyphitischen Umwandlung, einen Reaktionssaum zwischen grobkörnigem Spinell und Pyroxenen, mit denen er in Kontakt ist. Der übergang vom Spinell-Pyroxenit- zum Granat-Pyroxenit-Feld kann auf isobarische Abkühlung von höheren (magmatischen ?) Temperaturen zurückgehen. Granat-Pyroxen-Geothermometrie zeigt, dass die letzte Equilibrierung sehr wahrscheinlich bei P = 1.0 GPa (ca.), T = 750°C (ca.) erfolgte.Der zweite Typ von Granat-führenden Pyroxeniten ist ein (b) Orthopyroxenführender Granat-Spinell-Klinopyroxenit, der komplexe Texturen zeigt. Er besteht aus Zonen von grobkörnigem Klinopyroxen mit Einschlüssen von idiomorphem Spinell, der in Zonen übergeht, wo kleine gerundete Kristalle des gleichen Pyroxens und Spinells in relativ große Bereiche von extensiv kelyphitisiertem Granat (Py_64,8 Alm_25,6 Gr_9,6) eingeschlossen sind. Granat kommt auch als einschlußfreie Körner mit bis zu 4 mm Durchmesser vor. P-T Berechnungen geben wesentlich höhere Werte als für die Gesteine des Types (a). Die Entstehung der b-Typ-Granaten kann auch durch Subsolidus-Reaktion von Spinell und Pyroxen nach isobarischer Abkühlung von noch höheren Temperaturen beeinflußt sein; ein primärer magmatischer Ursprung könnte auch möglich sein, besonders für die körnigen Granate.P-T Abschätzungen für beide Pyroxenit-Typen sind gut einer Geotherme für 100 mW/m² Wärmefluß an der Oberfläche zuzuordnen. Ein solcher, relativ intensiver Wärmefluß könnte auf das Vorkommen von großen heißen Magmenkörpern hinweisen, die den lithosphärischen Mantel unter dem Iblei-Plateau und die untere Kruste in verschiedenen Niveaus intrudierten.

---

---

With 4 Figures     

Aliphatic hydrocarbons in metasomatized gabbroic xenoliths from Hyblean diatremes (Sicily): Genesis in a serpentinite hydrothermal system

Many tholeiite gabbro xenoliths from the Hyblean tuff-breccia deposits (Sicily, southern Italy) present mineralogical and geochemical evidence for hydrothermal alteration at different temperatures and water/rock ratios. In some cases, the primary mineral assemblage has been entirely replaced by Na-rich alkali feldspar, chlorite/smectite interlayers, zeolites, aegirine–augite, titanite, zircon etc. Hence the chemical composition of such metasomatic rocks displays larger amounts of volatiles, alkalis, Zr, Hf, U, Th and lower Ca, Mg, Fe with respect to the original gabbro. Five hydrothermally altered gabbroic xenoliths were selected for thermal decrepitation and bulk gas analyses by quadrupole mass spectrometry. All the samples analyzed display the same Electron Impact-Direct Pyrolysis Mass spectra (EI-DPMS). These show a series of peaks differing by 14 mass units due to loss of methylene groups (–CH₂), by a fragmentation process typical of saturated aliphatic and aliphatic–aromatic hydrocarbons. In addition, Fourier Transform Infrared (FT-IR) spectra of the samples present several bands typical of vibration frequencies of aliphatic hydrocarbons. The high-molecular-weight hydrocarbons observed probably originated from Fischer–Tropsch-type (FT-t) synthesis in the high temperature section of a serpentinite-hosted hydrothermal system. This suggestion may lend support to the recent hypothesis regarding the original oceanic nature of the Hyblean lithospheric basement.     

Moisture source in the Hyblean Mountains region (south-eastern Sicily, Italy): Evidence from stable isotopes signature

Here the authors present results of an isotope study on precipitation collected during a 2-a period from a rain-gauge network consisting of 6 stations located at different elevations in the Hyblean Mountains (HM) region, in south-eastern Sicily. The slope of the local meteoric water line (δD = 6.50 δ¹⁸O + 9.87) obtained for the region suggests that precipitation is affected by evaporation during rainfall events. The main variations in rainwater isotope composition are due to seasonal effects and elevation. An average ²H excess value of +21.2‰ was found for precipitation events less affected by evaporation (i.e. when the rainfall was >65 mm/month). The spatial distribution of O isotope composition of precipitation shows a negative gradient from east and south to the inner areas. The depositional rate of Cl, used as a tracer of the origin of air masses, is highest at the coastal rain-gauges (SR and MRG stations) and lowest on the northern flank of the HM region (SC station). Based on these findings, a model is proposed for the origin of precipitation in the HM region, which assumes that a Mediterranean-derived component is the main source of moisture in the studied area. D/H and ¹⁸O/¹⁶O ratios of inferred meteoric recharge waters were also compared with the isotope composition of waters collected from the main local springs and wells. The best linear fit of the δ¹⁸O vs δD relationship for Hyblean groundwater is δD = 4.85 δ¹⁸O–2.01. The enrichment of heavy isotopes in Hyblean groundwater is probably due to evaporation occurring after precipitation events or to a recharging contribution from surface waters (lakes or rivers) enriched in heavy isotopes.     

Gabbroic xenoliths in tuff-breccia pipes from the Hyblean Plateau: insights into the nature and composition of the lower crust underneath South-eastern Sicily, Italy

Summary Crust-derived xenoliths hosted by Miocene basaltic diatremes in the Hyblean Plateau (south-eastern Sicily, Italy) provide new information regarding the nature of a portion of the central Mediterranean lower crust. These xenoliths can be divided into three groups: gabbros (plagioclase + clinopyroxene + Fe–Ti oxides ± apatite ± amphibole ± Fe-rich green spinel), diorites (An-poor plagioclase, clinopyroxene ± Fe–Ti oxides ± orthopyroxene) and mafic granulites (plagioclase + clinopyroxene + green spinel ± orthopyroxene ± Fe–Ti oxides). Gabbros form the main subject of this paper. They represent cumulates whose igneous texture has been locally obliterated by metamorphic recrystallization and shearing. They were permeated by Fe–Ti-rich melts related to tholeiitic-type fractional crystallisation. Incompatible element ratios (Zr/Nb = 5–26; Y/Nb = 1.4–11) indicate that these cumulate gabbros derived from MORB liquids. Late-stage and hydrothermal fluids caused diverse, sometimes important, metasomatic trasformations. Petrographic and geochemical comparison with gabbroids from well-known geodynamic settings show that the Hyblean lower crustal xenoliths were probably formed in an oceanic or oceanic-continent transition environment.     

内蒙古阿巴嘎旗新生代玄武岩中超镁铁岩包体的特征

内蒙古东部阿巴嘎旗及其以北地区第四纪更新世钠质碱性火山岩中发现的超镁铁岩包体,主要为尖晶石二辉橄榄岩、方辉橄榄岩、纯橄榄岩、橄榄二辉岩、尖晶石单斜辉石岩和单斜辉石巨晶以及辉长岩、花岗闪长岩、石英长石片麻岩等壳源包体。超镁铁岩包体和巨晶的岩相学特征显示它们不是寄主玄武岩岩浆分离结晶堆积体;其主要元素、稀土元素特征与阿尔卑斯型橄榄岩相似,其组成接近于原始地幔岩值;同位素地球化学特征表明它们与寄主岩-玄武岩浆不是同源的;尖晶石二辉橄榄岩包体形成的平衡温度和压力范围分别为1056．9℃-1103．1℃,压力为1．50～1．84GPa,形成相当深度为49．5～60．72km。辉石岩包体形成温度为887．1℃-958．6℃,压力为1．25～1．4GPa,形成相当深度为41．25—46．2km。寄主玄武岩形成温度1390℃-1450℃,压力1．75—2．20GPa,形成相当深度为60—70km。可以认为,研究区在新生代发生了软流圈地幔上涌,导致岩石圈减薄以及地壳的拉张,大量岩浆物质沿构造通道溢出地表。其中超镁铁岩包体与寄主玄武岩浆之间没有熔体与残余物这种成因联系,它们是寄主玄武岩浆在上升过程中捕获的岩石圈地幔碎块。     

Petrological significance of high-pressure ultramafic xenoliths from ultrapotassic rocks of Central Italy

Two suites of ultramafic xenoliths have been found in ultrapotassic lavas from the 0.9 Ma old Torre Alfina volcano sited at the northern border of the Vulsinian district (Central Italy). One group of Xenoliths consists of spinel-bearing lherzolites, harzburgites, minor wherlites and dunites with a maximum size of 3–4 cm. Some samples contain discrete laths of phlogopite. A second class consists of phlogopite-rich, glass-bearing peridotites. The first suite displays textural characteristics such as triple points, deformed olivine with well developed kink banding and porphyroclastic textures indicating equilibration at high pressure. Pressure estimates give values in the range 1.3–2.5 GPa, corresponding to mantle depths in the area, where the present-day Moho is about 25 km deep. Equilibration temperatures have been estimated in the range between 950–1000°C. The chemical composition of some phases, such as the very high Fo contents of olivines (up to Fo₉₄ in harzburgites), Mg content of orthopyroxenes and Cr/Cr+Al ratios of clinopyroxenes and spinels, suggest that these xenoliths represent peridotites which suffered different degrees of partial melting before being incorporated into the Torre Alfina magma. On the other hand, the occurrence of phlogopite speaks for metasomatic events. The phlogopite-rich, glass-bearing xenoliths consist of phlogopite, olivine, clinopyroxene, rare orthopyroxene and glass. Apatite is the most common accessory. Olivine is present in both euhedral and strained crystals. A few relics of protogranular textures are also observed. Textural and chemical evidence suggests that these xenoliths represent mica-rich peridotites which have undergone phlogopite breakdown during rapid rise to the surface with the development of a K-rich liquid which reacted with mafic phases producing a rapid growth of olivine and, to a lower extent, pyroxene. Originally, these xenoliths may have represented intensively metasomatized upper mantle. However, a cumulitic origin from previous potassic magmatic events cannot be excluded. The host lavas have compositions intermediate between high-silica lamproite and Roman-type ultrapotassic rock. They have high abundances of incompatible elements and radiogenic Sr, coupled with high Mg content, MgO/CaO, Ni and Cr. These features support a genesis in a residual upper mantle which has suffered partial melting with the extraction of basaltic liquids, followed by metasomatic events which caused an enrichment in incompatible elements and radiogenic Sr. The presence of mantle-derived ultramafic xenoliths in the torre Alfina lavas testifies for a rapid uprise of the magma which reached the surface without suffering fractional crystallization and significant interaction with the upper crust. Accordingly, the Torre Alfina lavas represent an unique example of primitive potassic liquid in Central Italy.     

Geochemistry and potential use of groundwater in the Rocca Busambra area (Sicily, Italy)

In the Rocca Busambra area (mid-west Sicily, Italy), from November 1999 to July 2002, 23 water points including wells and springs were sampled and studied for their chemical and isotopic compositions. Two rain gauges were also installed at different altitudes, and rainwater was collected monthly to determine the isotopic composition. The obtained results revealed the Rocca Busambra carbonate complex as being the main recharge area on account of its high permeability value. From a chemical view point, two main groups of water can be distinguished: calcium–magnesium–bicarbonate-type and calcium–magnesium–chloride–sulphate-type waters. The first group reflects the dissolution of the carbonate rocks; the second group probably originates from circulation within flyschoid sediments. Three water wells differ from the other samples due to their relatively high Na and K content, which probably is to be referred to a marked interaction with the “Calcareniti di Corleone” formation, which is rich in glauconite [(K, Na)(Fe³⁺, Al, Mg)₂(Si, Al)₄O₁₀(OH)₂]. In accordance with WHO guidelines for drinking water (2004), almost all the samples collected can be considered drinkable, with the exception of four of them, whose NO₃ ⁻, F⁻ and Na⁺ contents exceed the limits. On the contrary, the sampled groundwater studied is basically suitable for irrigation.     

Geochemical characteristics of waters in mineralised area of Peloritani Mountains (Sicily,Italy)

This paper presents the results of a study on the geochemistry of waters circulating in the mineralised area of the south-eastern sector of Mt. Peloritani (north-eastern Sicily, Italy), aimed at basic understanding of the geochemical processes influencing their chemical composition. Chemico-physical parameters and data on 26 major and minor chemical elements are reported for 103 water samples. Water chemistry is mainly dominated by dissolution of carbonates and hydrolysis of aluminosilicate minerals. Total dissolved salts (TDS) range from 80 to 1398 mg/L. All the waters exhibit E_H characteristic of an oxygenated environment. Excluding two samples, which show very high H⁺ activity (pH = 3.0 and 2.7), all the waters have pH values in the range 6.2–8.6. Cluster analysis based on major ion contents defined three main chemical water types, reflecting different hydrochemical processes. The first, group I, has low salinity (average TDS = 118 ± 30 mg/L) and abundance orders (meq/L) Na > Ca ≈ Mg > K and Cl ≈ HCO₃ > SO₄. With increased water–rock interaction, waters in groups II and III become more saline, changing composition towards SO₄–Cl-alkaline earth and HCO₃-alkaline earth types. Weathering of carbonate minerals causes waters to become saturated with respect to calcite and dolomite, whereas the incongruent dissolution of aluminosilicate minerals causes the solution to reach equilibrium with kaolinite and to form smectites. Trace element geochemistry in the analysed waters reflects interactions between waters and existing mineralisation, with elemental concentrations showing highly variable values, and higher concentrations of As, Pb, Sb and Zn near known mineralisation. Lead–Zn and As–Sb statistical associations, probably distinguishing interactions with different mineralogical phase paragenesis, were revealed by factor analysis. The main aqueous chemical forms of trace elements predicted by chemical speciation calculations are also reported. As most of the analysed spring waters provide the main source of freshwater for domestic purposes, attention should be given to As and Sb, whose concentrations exceed the recommended limits.     

Noble gases in ultramafic xenoliths from San Carlos,Arizona

This work reports the results of noble gas (Ne, Ar, Kr, Xe) analyses of accidental mantle xenoliths from San Carlos, Arizona. Except for the addition of radiogenic ⁴⁰Ar and mass fractionation effects, the isotopic structures of these gases are indistinguishable from atmospheric composition. The absence of ¹²⁹Xe excesses in these rocks may reflect indirect mixing of atmospheric gases with the source region of the xenoliths. The dominant influence on the noble gas abundances in the San Carlos xenoliths appears to have been diffusive gas loss, which may have occurred in a mantle metamorphic event or during contact with the host basanite magma. Evidence is presented for the partitioning of significant amounts of the heavy noble gases into fluid inclusions in the xenolith minerals; the proportion of each gas in the inclusions increases with increasing atomic weight of the gas, possibly reflecting solubility effects. The noble gases are present in greater concentration in pyroxenes than in olivine, similar to the behavior of other incompatible elements.     

Petrology of recrystallized ultramafic xenoliths from Merelava volcano,Vanuatu

Xenoliths in primitive olivine tholeiite lavas from Merelava Volcano, Vanuatu, include recrystallized wehrlites and harzburgites characterized by extremely fine grain size (0.02–2 mm) and equigranular textures. The harzburgites display mineral segregations, have highly variable ratios of ol: opx, minor clinopyroxene and accessory Cr-spinel, and are interpreted as the residues of high degrees of melting of upper mantle peridotite. Annealed Cr-spinel aggregates in harzburgite sample # 31564B enclose numerous small inclusions of sodic sanidine and minor plagioclase, attributed to infiltration of the harzburgite by a residual melt derived from an earlier period of island arc magmatism. The recrystallized wehrlites have high ol/cpx ratios and depleted REE patterns compatible with a cumulus origin. The refractory nature of the phases in both groups of recrystallized xenoliths compares closely with phases in Alpine-type peridotites and primitive arc lavas, and is incompatible with compositions of abyssal peridotites. The recrystallized wehrlites give equilibration temperatures of 1070–1130° C and are interpreted as cumulates derived from an earlier period of Vanuatu Arc magmatism. The range of composition displayed by phases in the harzburgites is greater than phase variation in the wehrlites, and reflects a more complex thermal history. Textural, mineralogical, and geothermometric considerations indicate the harzburgites underwent cooling to 800°/900° C before being re-heated to 1000–1100° C by the current magmatic regime. A shallow crustal origin for these xenoliths is indicated by gravity data and tectonic considerations which strongly imply the presence of an ophiolite body beneath Merelava, representing the northward extension of the Pentecost Ophiolite. These interpretations are compatible with a published model for generation of the host basalts by partial melting at the crust/mantle boundary (ca. 17 km). Sr isotopic data show that the harzburgites are incompatible with residues of ocean-floor magmatism, or with residues of Merelava and Central Chain magmatism, but suggest an affinity with Vitiaz Arc magmatism of Eocene-lower Miocene age. Both groups of xenoliths were apparently entrained from wall rocks during ascent of the host magmas.     

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

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

Different styles of metasomatic veining in ultramafic xenoliths from the TUBAF Seamount (Bismarck Microplate,Papua New Guinea)

Petrologic, geochemical and isotopic investigations on two ultramafic xenoliths with metasomatic veins from the TUBAF Seamount in the Bismarck Archipelago NE of Papua New Guinea reveal different styles of metasomatic overprinting. The first xenolith, a clinopyroxene–poor spinel lherzolite, was part of the depleted upper mantle. It contains an orthopyroxene-rich vein that formed by hydrous metasomatism at ~ 980 °C and ~ 1.5 GPa. The second xenolith is a clinopyroxene-dominated spinel olivine websterite that formed as a magmatic cumulate at the transition of the upper mantle to the oceanic crust. The websterite contains a vein with orthopyroxenes and clinopyroxenes, which give evidence for high-temperature crystallization at ~ 1300 °C and < 0.36 GPa. Both xenoliths were transported to the seafloor by a Quaternary trachybasalt in a fore-arc position. The vein minerals show a strong affinity to a supra-subduction zone or island arc setting. The REE pattern of the vein in the clinopyroxene–poor lherzolite strongly resembles the one from the host trachybasalt, with a high enrichment of the LREE and a strong to moderate enrichment of the MREE and HREE. Although broadly similar in shape, the REE pattern of the vein in the websterite shows a much weaker enrichment. The same applies to the trace-element patterns, although there are significant differences in the Eu, Zr, Hf and Nb concentrations. The isotope signatures of both veins suggest a derivation from a subducted slab that had been hydrothermally altered by seawater (high ⁸⁷Sr/⁸⁶Sr values).The contrasting crystallization temperatures of the vein minerals as well as their overall geochemical differences indicate that the metasomatic agents responsible for the vein in the websterite were mobilized from a previously depleted source at a much deeper mantle level than those forming the vein of the clinopyroxene–poor lherzolite. The metasomatic agents may also have been mobilized at different times and from different plates, i.e., the deeply subducted Solomon Sea Microplate (for the veins in the websterite) and the shallow dehydrating Pacific Plate (for the veins in the clinopyroxene–poor lherzolite).Metasomatic agents responsible for similar petrologic phenomena, i.e., modal or cryptic metasomatism, may have distinctly different origins and show contrasting histories. A strongly depleted lherzolite may totally lose its initial geochemical signature by the influence of an enriched metasomatic agent, whereas a primarily enriched ultramafic rock, e.g., a websterite, may strongly obscure the trace-element pattern of a less enriched metasomatic vein. Furthermore, the geochemistry of the ultramafic xenoliths may reflect polyphase cryptic and modal metasomatism related to veining and later transport by the hosting melt to the seafloor.     

Petrology of ultramafic xenoliths from Kishyuku Lava,Fukue-jima,Southwest Japan

 Ultramafic xenoliths are found in Kishyuku Lava, Fukue-jima, Southwest Japan. These include spinel lherzolite, harzburgite and dunite, as well as pyroxenite. The compositions of the constituent minerals of the peridotite xenoliths are in the range of upper mantle peridotites. Variable Cr/(Cr+Al) ratios (0.1–0.5) of spinel, together with a limited range in olivine composition (Fo₉₀–Fo₉₂), indicate that the xenoliths are derived from slightly to highly depleted residual mantle. The combination of previously published clinopyroxene-olivine geothermobarometry and clinopyroxene-orthopyroxene geothermometry applied to the xenoliths yields a high geotherm of 1070° C at 1.0 GPa up to 1200° C at 2.2 GPa. Existence of such depleted upper mantle is compatible with the existing model of asthenospheric injection during the rifting of the Northeast China and the Japan Sea. The high geotherm is caused by thermal perturbation due to the injection of the hot asthenosphere and/or post-rifting uprise of mantle diapirs since 11 Ma. Received: 15 May 1995 / Accepted: 3 January 1996     

Metasomatic coronas around hornblendite xenoliths in granulite facies marble, Ivrea zone, N Italy. II: Oxygen isotope patterns

Up to 20-cm-wide metasomatic reaction bands formed coronas around hornblendite xenoliths in a marble matrix during high grade metamorphism in the Ivrea zone. The coronas are comprised of an innermost monomineralic clinopyroxene layer, a garnet-clinopyroxene layer and an outermost scapolite-clinopyroxene layer. The oxygen isotope composition of the original hornblendite core is 7‰ relative to V-SMOW and the oxygen isotope composition of the marble matrix is 19.7‰. The oxygen isotope transition across the corona is represented by a diffusion front with a step discontinuity at the inner margin of the corona. The systematics of the inter-mineral fractionations indicates preservation of the oxygen isotope compositions from high temperatures and maintenance of grain-scale oxygen isotope equilibrium during corona formation. The oxygen isotope pattern is interpreted in terms of a moving boundary diffusion problem. The growing reaction band and the reactant hornblendite and marble represent a total of five media with different transport properties and moving separation surfaces. Bulk oxygen diffusion was at least three orders of magnitude faster then expected from volume diffusion, suggesting that transport was enhanced by relatively fast diffusion along grain boundaries. Oxygen diffusivities in the individual layers correlate with the oxygen volume diffusivities in the major constituent minerals of the respective layers, suggesting mineralogical control on bulk oxygen diffusion.     

Comparative study of ultramafic xenoliths and associated lavas from South-Eastern Sicily: nature of the lithospheric mantle and insights on magma genesis

Isotope analyses of lavas from the Hyblean Plateau (SE Sicily) provided first order constraints for the characterization of the relative magma sources, contributing to a better understanding of the tectono-magmatic evolution of the northernmost part of the African plate. To integrate this research, we are currently studying ultramafic xenoliths of mantle provenance exhumed by the Hyblean alkaline volcanics. These mainly consist of anhydrous spinel-facies peridotites and subordinate pyroxenites/websterites. The paragenesis of the latter is extremely variable in terms of modal proportions and mineral composition, with clinopyroxene composition ranging from Cr-diopside to Al-augite, and variable amount of spinel ± garnet. New Sr-Nd isotopic analyses carried out on hand-picked (and leached) clinopyroxenes indicate that peridotites have ⁸⁷Sr/⁸⁶Sr ranging from 0.70288 to 0.70309, and ¹⁴³Nd/¹⁴⁴Nd from 0.51287 to 0.51292. This Sr-Nd isotopic fingerprint approaches that of the HIMU mantle end-member, regionally referred as EAR (European Astenospheric Reservoir) to emphasize a connection with a sub-lithospheric metasomatic component ubiquitous throughout Europe, the Mediterranean area and North Africa. The Sr-Nd analyses of pyroxenites also reveal an EAR affinity, but are slightly distinct from those of peridotites. They display ⁸⁷Sr/⁸⁶Sr ranging between 0.70305–0.70326 and ¹⁴³Nd/¹⁴⁴Nd between 0.51292–0.51299, overlapping the composition typical of the Hyblean alkaline lavas. This possibly implies that pyroxene-rich domain significantly contributed to the genesis of the Hyblean magmas. Therefore, the presented Sr-Nd isotopic ratios suggest that the role of the pyroxene-rich mantle portions was more important than commonly considered in the petrogenetic models of Hyblean magmas. This scenario would be coherent with recent evidences highlighting the importance of pyroxenites (together with peridotites) as contributing sources to basalt generation.     

滇西大理地区存在泛非期构造-热事件记录

大理地区存在较完整的新元古代泛非期构造-热事件记录,海东挖色花岗闪长岩、花岗岩中获得黑云母K-Ar年龄799Ma、锆石U-Pb年龄667Ma,苍山云弄峰黑云母二长花岗岩中获得锆石U-Pb年龄748Ma,大沟箐角闪辉长岩中获得K-Ar年龄892.3Ma。新元古代挖色花岗岩和云弄峰花岗岩与奥陶系大成村组沉积接触。大成村组粉砂岩中产腕足类、腹足类化石,顶部与中志留统阴阳山组假整合接触,缺失下志留统。向阳村奥陶系—志留系发育较好,产丰富的三叶虫、笔石化石,其中不乏早奥陶世的标准分子。大理地区的地层构造与丽江地区差异较大,不能对比,但可以同青海南部及藏东对比。古中元界苍山群相当于宁多群,新元古界罗平山岩组相当于草曲群,缺失震旦系—寒武系。下奥陶统向阳组、迎凤村组相当于青泥洞组和曾子顶组。因此,大理地区板坱构造划分应归属西藏-三江造山系中的扬子西缘多岛-弧-盆系。西藏-三江造山系与扬子-华南陆块区的界线应移至红河-程海断裂上。     

Metasomatic coronas around hornblendite xenoliths in granulite facies marble, Ivrea zone, N Italy, I: constraints on component mobility

Centimeter- to decimeter-thick reaction bands occur at hornblendite/marble interfaces in Val Fiorina in the granulite facies metamorphic Ivrea zone. From hornblendite to marble the reaction bands show a consistent succession of sharply bounded mineral layers comprising a monomineralic clinopyroxene layer, a garnet-clinopyroxene layer and a scapolite-clinopyroxene layer. Reaction band formation occurred as a response to gradients in the chemical potentials of calcium and magnesium as defined by the hornblendite assemblage and the marble matrix. The metasomatic corona primarily replaced the hornblendite, and only minor amounts of marble were consumed. The reaction band behaved as an open system with net transfer of calcium from the marble into the reaction band, and a net transfer of iron and magnesium in the opposite direction. Mass balance considerations allow us to constrain a range of feasible mass balance scenarios for which major element fluxes across the boundaries of the reaction band may be quantified. Modeling of layer growth as a steady diffusion process yields ratios of the phenomenological diffusion coefficients for Si, Al, Mg, and Ca of ${{L_{SiSi} } \over {L_{CaCa} }}> 2.5,{\kern 1pt} {\rm }{{L_{AlAl} } \over {L_{CaCa} }}<10,{\rm }{{L_{MgMg} } \over {L_{CaCa} }}> 1.${{L_{SiSi} } \over {L_{CaCa} }}> 2.5,{\kern 1pt} {\rm }{{L_{AlAl} } \over {L_{CaCa} }}<10,{\rm }{{L_{MgMg} } \over {L_{CaCa} }}> 1. . The relative diffusivities are primarily constrained by the sequence of mineral layers of the reaction band and by the relative thickness of the layers. The results of steady-state diffusion modeling are relatively insensitive with respect to variations in the major element boundary fluxes.     

Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano,Hawaii

Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225° to 1350° C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045° and 1090° C. Comparisons of the abundance of K₂O in plagioclase and the abundances of TiO₂ and Fe₂O₃in spinel of xenoliths and mid-ocean ridge basalt, and a single ⁸⁷Sr/ ⁸⁶Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155°–230° C of cooling which took place over about 120 ka — the age of the youngest Hualalai tholeiitic basalt — yield maximum cooling rates of 1.3×10^–3–1.91×10^–3 °C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel.     

Metasomatic interactions between slab-derived melts and depleted mantle: Insights from xenoliths within Monglo adakite (Luzon arc, Philippines)

The Monglo adakite contains mafic and ultramafic xenoliths, which probably originated from the mantle section of an Early Cretaceous supra-subduction zone ophiolitic complex located within the Luzon arc crust. Spinel-bearing dunites are dominant among this xenolith collection and display evidence for three episodes of subduction-related melt percolation. The first one is evidenced by an undeformed clinopyroxene characterized by convex-upwards REE pattern. This clinopyroxene crystallized from a calc-alkaline basaltic magma, likely formed in the Cretaceous supra-subduction setting of the ophiolite. Then, two metasomatic events, evidenced by orthopyroxene-rich and amphibole-rich secondary parageneses, respectively, affected most of the spinel dunites. The opx-rich paragenesis is related to the circulation within the dunitic upper mantle of hydrous slab-derived melts similar to those affecting the mantle peridotite xenoliths from Papua New Guinea and Kamchatka. Finally the amphibole-rich veins are related to the interaction between the studied dunite xenoliths and the host adakite or an adakitic melt similar to it.