Rare earth evidence concerning the origin of granites of the Isle of Skye,northwest Scotland

Eleven samples of Skye granites, two samples of Torridonian sandstone and one sample of Lewisian gneiss have been analysed for ten rare earth elements (REE) by neutron activation analysis. The granites are representative of the main granite centres and compositional types. All granites have sub-parallel light-REE-enriched patterns with chondrite-normalised Ce(Ce_N) = 78–263,Yb_N = 16–60and Ce_N/Yb_N = 2.9–8.0. REE patterns for the Lewisian gneiss and Torridonian sandstone are similar to each other, withCe_N = 32–61,Yb_N = 3–5and Ce_N/Yb_N = 8–18. These two rock types as well as the Glamaig granite have negligible Eu anomalies (Eu/Eu* > 0.9), and the other granites have Eu/Eu* in the range 0.83-0.34. The REE evidence suggests that Lewisian gneiss or Torridonian sandstone arenot suitable materials from which the granites could be derived by partial melting. The Western Red Hills granite intrusions show a systematic relation of REE content with Eu/Eu*. We suggest that the Glamaig granite is the most primitive, and was derived from a source with no Eu anomaly by fractional crystallization of a more basic magma. The later Western Red Hills granites might then have resulted from further fractional crystallization of magma with a composition like that of the Glamaig granite. The Coire Uaigneich and Eastern Red Hills granites may also be products of fractional crystallization, but from different magmas to those parental to the Western Red Hills granites. The basaltic parent magmas of the Skye granites may be “continental” tholeiites derived by interaction of basalt magma with Lewisian gneiss.     

A geochemical study of island-arc and back-arc tholeiites from the Scotia Sea

⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios, REE and selected minor and trace elements are presented and compared for present-day volcanic rocks in the Scotia Sea.Tholeiitic basalts from the South Sandwich Islands show widely ranging contents of some lithophile elements, e.g. K₂O (0.09–0.55%) and Rb (1.55–14.2 ppm), but fairly constant Na₂O and Sr. Total REE contents range from about 4–20 times chondritic abundances with significant light-REE depletion and both positive and negative Eu anomalies. The variations in minor and trace element abundances are consistent with low-pressure fractional crystallization of plagioclase and clinopyroxene but only minor amounts of olivine. The⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios of the parental magmas are thought be 0.7038–0.7039 and 0.51301–0.51314 respectively, and indicate derivation of at least some⁸⁷Sr from subducted ocean crust.The back-arc tholeiites in the Scotia Sea have lower⁸⁷Sr/⁸⁶Sr ratios (0.7028–0.7033), similar¹⁴³Nd/¹⁴⁴Nd ratios (0.51305) and are variably light-REE-enriched(Ce_N/Yb_N= 1.0–1.6). Total REE contents are comparable to those of the South Sandwich Islands tholeiites.     

Geochemistry of the Middle to Late Permian limestones from the marginal zone of an isolated platform (Laibin, South China)

Major, trace and rare earth elements were measured in 27 samples of the Middle to Late Permian limestones from the Tieqiao section located on the marginal zone of an isolated platform (Laibin, South China). Shale-normalized REE+Y patterns of all samples show notably negative Ce anomalies (0.21–0.66, average 0.33), slightly positive Gd anomalies (1.08–1.30, average 1.20), and positive Y anomalies with superchondritic Y/Ho ratios (36–91, average 55), which are consistent with those of modern shallow seawater. Their relative LREEs enrichment with higher Nd_SN/Yb_SN ratios (0.58–1.80) than those of modern shallow seawater (0.21–0.50) suggests complicated sources of REEs for all samples. Compared with geochemical features of sediments influenced by terrigenous particles and hydrothermal fluids, it is concluded that ambient shallow seawater was the primary source of REEs in these limestones. Comparing the indicators of REE+Y elements (ΣREE, Nd_SN/Yb_SN, Ce/Ce*, Gd/Gd*, Eu/Eu* and Y/Ho) in limestones with those in bedded cherts from the Tieqiao section, we consider that limestone and bedded chert have similar sources of REE+Y elements: ambient shallow seawater with more or less hydrothermal fluids. In addition, there is a completely negative correlation between CaCO₃ and SiO₂ contents in limestones and bedded cherts. These results imply that precipitation of CaCO₃ was inhibited by that of SiO₂ which was derived mainly from hydrothermal fluid, especially in bedded cherts from the Tieqiao section.     

Rare earth and strontium isotope evidence concerning the petrogenesis of North Chilean ignimbrites

New rare earth element (REE) data, Rb and Sr analyses and Sr isotope measurements are presented for pumice clasts collected from some North Chilean ignimbrites of dacite and rhyolite composition. The samples are light-REE enriched with chondrite-normalised Ce (Ce_N) of 17–98, Yb_N of 4–14 and Ce_N/Yb_N of 2.6–15. While some samples have no Eu anomalies, others do have anomalies with inferred Eu/Eu^* values of down to ca. 0.4. Eleven samples have present-day⁸⁷Sr/⁸⁶Sr ratios between 0.7053 and 0.7100, and noting that some samples are up to 12 Ma old, initial⁸⁷Sr/⁸⁶Sr ratios are below ca. 0.709. These trace element and Sr isotope characteristics resemble those of contemporaneous andesite and dacite lavas, suggesting a common origin for all these rock types. The higher Rb/Sr ratios and larger Eu anomalies in most of the dacitic and rhyolitic ignimbrites are consistent with an origin by plagioclase-dominated fractional crystallization of mantle-derived andesite magma.     

Bearing of rare earth patterns of apatites from igneous and metamorphic rocks

Twelve apatite samples from igneous and metamorphic rocks from the Black Forest and igneous rocks from the Kaiserstuhl were analysed for their REE content. The ΣREE range from 0.116 to 1.69 wt.%; the lowest values were found in the metamorphic rocks. All apatites from the various parent rocks show a general enrichment of the lighter rare earths over the heavier and their chondrite-normalized rare earth patterns exhibit a more or less pronounced negative Ce anomaly. This Ce depletion is accompanied by relatively low La and Pr values. In addition, the apatites from igneous rocks from the Black Forest show a marked negative Eu anomaly. An explanation is offered for the simultaneous occurrence of a negative Ce and a negative Eu anomaly in one investigated rock system. The negative Ce anomaly is attributed to the occurrence of phases enriched in Ce (e.g., monazite, allanite) which crystallized prior to or simultaneously with apatite. The negative Eu anomaly in these magmatic apatites most probably is caused by discrimination of Eu²⁺ from the apatite lattice. The result of this discrimination is a selective Eu enrichment in the later crystallizing feldspars, plagioclase and orthoclase. At least in this case, the positive Eu anomaly in feldspars is not a reliable indicator of low oxygen fugacity during their crystallization; the Eu depletion of the earlier crystallized apatites is preferable for this purpose.     

Zircon U-Pb and geochemical analyses for leucocratic intrusive rocks in pillow lavas in the Danfeng Group,north Qinling Mountains,China

Field observation showed that there are many irregular leucocratic intrusive rocks in pillow lavas in the Danfeng Group in the Xiaowangjian area, north Qinling orogenic belt. Photomicrographs indicated that the protoliths of those altered leucocratic intrusive rocks are dioritic rocks. Geochemical analyses showed that pillow lavas have a range of SiO2 from 47.35% to 51.20%, low abundance of TiO2 from 0.97% to 1.72%, and percentages of MgO (MgO#=41―49). Chondrite-normalized REE patterns of pillow lavas are even, indicative of a weak differentiation between LREE and HREE (La/YbN=1.52―0.99). N-MORB-normalized trace element abundances showed that pillow lavas are enriched in incompatible elements (e.g., K, Rb, and Ba). Leucocratic intrusive rocks in pillow lavas have a wide range of SiO2 from 53.85%―67.20%, low abundances of TiO2 from 0.51%―1.10%, and MgO (MgO#=40―51), and higher percentages of Al2O3 (13.32%―16.62%) and concentration of Sr (342-539 μg/g), ratios of Na2O/K2O (2―7) and Sr/Y (17―28). Chondrite-normalized REE patterns of leucocratic intrusive rocks showed highly differentiation between LREE and HREE (La/YbN=12.26―19.41). N-MORB-normalized trace element abundances showed that leucocratic intrusive rocks are enriched in incompatible elements (e.g., K, Rb, and Ba), and significantly depleted in HFSE (e.g., Nb, Ta, Zr and Ti), indicative of a relationship to subduction. Isotopically, leucocratic intrusive rocks have a similar εNd(t) ( 7.45― 13.14) to that of MORB ( 8.8― 9.7), which indicates that those leucocratic intrusive rocks sourced from depleted mantle most likely. SHRIMP U-Pb analyses for zircon showed that those leucocratic intrusive rocks were formed at 442±7 Ma, yielding an age of subduction in the early Paleozoic in the north Qinling orogenic belt.     

Sedimentary geochemistry of the Cambrian-Ordovician cherts: Implication on archipelagic ocean of North Qilian orogenic belt

The Caledonian North Qilian orogenic belt lies between the North China plate and the Qaidam mi-croplates, and resulted from the collision among the Qaidam microplate, mid-Qilian block and the North China plate. The orogen initiated from the rifting of the Late Proterozoic Rodinia, and then it experi-enced stages of Cambrian rift basin and Ordovician archipelagic oceanic basin, and foreland basin during Silurian to Early-Middle Devonian. The average ratios of Al/(Al Fe Mn), Al/(Al Fe), δ Ce, Lan/Ybn and Lan/Cen from cherts of Cambrian Heicigou Formation are 0.797, 0.627, 1.114, 0.994 and 1.034 re-spectively. In the NAS standardized REE distribution pattern, the cherts from Xiangqianshan is slightly HREE enriched, and the cherts from Ganluci and Shiqingdong are plane. All of these features indicated that Cambrian cherts of the Heicigou Formation originated from a continental margin rift background. On the contrary, the average ratios of Al/(Al Fe Mn), Al/(Al Fe), δ Ce, Lan/Ybn, Lan/Cen of the Ordovician chert from Dakecha, Cuijiadun, Shihuigou, Laohushan, Heicigou, Maomaoshan, Bianmagou, Da-chadaban, Baiquanmen, Jiugequan and Angzanggou, are respectively 0.72, 0.58, 0.99, 1.09 and 0.96 respectively. Their NAS standardized REE distribution patterns of most Ordovician cherts are plane mode or slightly HREE enriched. The REE distribution pattern of few samples of cherts are slightly LREE enriched. Characteristics of sedimentary geochemistry and tectonic evolution demonstrated that the Cambrian-Ordovician cherts, associated with rift, oceanic, island arc and back-arc volcanic rocks, was not formed in a typical abyssal oceanic basin or mid-oceanic ridge. On the contrary, they formed in a deepwater basin of continental margin or a archipelagic ocean tectonic setting. Several Early Paleo-zoic ophiolite belts in North Qilian and adjacent periphery Qaidam microplate imply that an archipelagic ocean during Ordovician existed in the east of Pro-Tethys.     

Rare-earth element and heavy-metal behaviour associated with the epithermal gold deposit on Lihir Island, Papua New Guinea

A thick sequence of alkaline intrusions and volcanic rocks underlies a Quaternary caldera on Lihir Island. The sequence is host to a still-active subaerial hydrothermal system and associated epithermal gold mineralization. Chondrite-normalized (La/Lu)_cn and (La/Sm)_cn ratios progressively increase up the alteration sequence from the potassic alteration zone, to the argillic zone to the advanced argillic zone. (Tb/Lu)_cn ratios only significantly increase in argillic and advanced argillic assemblages. Surface oxide alteration lithologies and acid sulphate water precipitates possess distinctly lower (La/Lu)_cn and (Tb/Lu)_cn ratios than the underlying subsurface alteration units. The changes in the REE, LREE and HREE fractionation trends from subsurface to surface alteration zones reflect the transition from a magmatic-hydrothermal, neutral chloride fluid regime at depth to acid sulphate meteoric waters in the upper portion of the alteration profile.Boiling of the LREE-Eu-enriched magmatic fluids occurred at a depth of at least 750 m. It is proposed that pronounced differential flow rates of the vapour and liquid phases and solution chemistry changes approximately above 300–350 m caused the incorporation of LREE and Eu into anhydrite-calcite veins and the deposition of LREE and HREE into wallrocks of upper parts of the potassic alteration unit. Condensation of the vapour phases into meteoric waters gave rise to low-temperature acid fluids that deposited large amounts of LREE within argillic and advanced argillic alteration units. This was also accompanied by HREE mobility due to large fluid volumes, acid fluid conditions and abundant sulphate complexes within the solutions. The HREE were either lost from the hydrothermal system or deposited in oxide assemblages and acid sulphate water precipitates.     

Terminal Ediacaran anoxia in deep-ocean: Trace element evidence from cherts of the Liuchapo Formation,South China

Here we report a detailed trace element study of the cherts from Liuchapo Formation, which is a terminal Ediacaran (551-542 Ma) succession in South China deposited in deep-water basinal setting. The REE of Liuchapo cherts shows similar features as observed for anoxic modern seawater (but not for hydrothermal fluids), characterized by positive La anomaly (La_N/Ce_N = 0.83–1.91, average 1.37), moderately negative Ce anomaly (0.53–1.1, average 0.73), positive Gd anomaly (average 1.08), positive Y anomaly (average 1.21), and depleted LREE and MREE. In addition, the Liuchapo cherts have low ΣREE (3.36–56.13 ppm, average 20.6 ppm), low Al₂O₃, Ti, Th and Zr concentrations, and high Y/Ho ratios (up to 43.9). The redox-sensitive trace elements concentrations in the cherts do not correlate with detrital input proxies. All of these features suggest that the redox-sensitive trace elements in the cherts were authigenically concentrated in water column and their concentrations thus are excellent indicators of ancient redox conditions. Very low Th/U ratios, high V/(V+Ni) and Fe_⊤/Al ratios, enrichments of redox-sensitive trace elements (U, V, Mo), and low concentration of Mn in the cherts imply anoxia in the deep seawater. Our data reveal that the terminal Ediacaran ocean was not completely oxidized and the deep ocean was still anoxic, at least in South China. We propose that although the oxidative events existed in the terminal Ediacaran oceans, decomposition of organic matter prolonged anoxia in the deep ocean. Supported by National Natural Science Foundation of China (Grants Nos. 40532012, 40873007, 40603021) and Chinese Academy of Sciences (Grant No. KZCX3-SW-141)     

143Nd/144Nd,87Sr/86Sr and trace element constraints on the petrogenesis of Aleutian island arc magmas

¹⁴³Nd/¹⁴⁴Nd,⁸⁷Sr/⁸⁶Sr and trace element results are reported for volcanic and plutonic rocks of the Aleutian island arc. The Nd and Sr isotopic compositions plot within the mantle array with ε_Nd values of from 6.5 to 9.1 and⁸⁷Sr/⁸⁶Sr ratios of from 0.70289 to 0.70342. Basalts have mildly enriched light REE abundances but essentially unfractionated heavy REE abundances, while andesites exhibit a greater degree of light to heavy REE fractionation. Both the basalts and andesites have significant large ion lithophile element to light rare earth element (LILE/LREE) enrichments. Variations in the isotopic compositions of Nd and Sr are not related to the spatial distribution of volcanoes in the arc, nor are they related to temporal differences. ε_Nd and⁸⁷Sr/⁸⁶Sr do not correlate with major element compositions but do, however, correlate with certain LILE/LREE ratios (e.g. Ba_N/La_N). Plutonic rocks have isotropic and trace element characteristics identical to some of the volcanic rocks. Rocks that make up the tholeiitic, calc-alkaline and alkaline series in the Aleutians do not come from isotopically distinct sources, but do exhibit some differing LILE characteristics.Given these elemental and isotopic constraints it is shown that the Aleutian arc magmas could not have been derived directly from homogeneous MORB-type mantle, or fresh or altered MORB subducted beneath the arc. Mixtures of partially altered MORB with deep-sea sediment can in principle account for the isotopic characteristics and most of the observed LILE/LREE enrichments. However, some samples have exceedingly high LILE/LREE enrichments which cannot be accounted for by sediment contamination alone. For these samples a more complex scenario is considered whereby dehydration and partial melting of the subducted slab, containing less than 8% sediment, produces a LILE-enriched (relative to REE) metasomatic fluid which interacts with the overlying depleted mantle wedge. The isotopic and LILE characteristics of the mantle are extremely sensitive to metasomatism by small percentages of added fluid, whereas major elements are not substantially effected, Major element compositions of Aleutian magmas are dominantly controlled by the partial melting of this mantle and subsequent crystal fractionation; whereas isotopic and LILE characteristics are determined by localized mantle heterogeneities.     

Origin of the Gangdise (Transhimalaya) Permian arc in southern Tibet: Stratigraphic and volcanic geochemical constraints

The well‐studied Mesozoic and Cenozoic volcanic rocks of the Gangdise Terrane, southern Tibet, are widely interpreted to have resulted from subduction of the Neotethys; however, Late Paleozoic volcanic rocks and their tectonic setting remain poorly studied. Based on new geological data, we carried out stratigraphical and geochemical analyses of Permian volcano‐stratigraphic sequences within an east–west‐trending, fault‐bounded zone of uplift in the central Gangdise Terrane. Sedimentary rocks in this area consist of platform carbonates and terrigenous clastic rocks that represent widespread shallow‐marine sedimentary basins developed around northern Gondwana. A regression or tectonic uplift event is recorded in Permian sedimentary rocks that show the local development of fluvial environments. The sedimentary succession contains evidence of two volcanic stages: a period of basaltic extrusions and younger explosive felsic magmatism. The first volcanic stage is Early and Middle Permian in age. Tholeiitic basaltic lavas are exposed around Maizhokunggar (Tangjia) and Lhunzhub in central Gangdise. The Lower Permian basalts are relatively enriched in MgO (4.58–12.19%), whereas the Middle Permian basalts are characterized by high Al₂O₃ contents (11.75–21.22%). Rocks of both ages are enriched in large‐ion lithophile elements (LILE) and light rare earth elements (LREE), and show pronounced negative Nb and Ta anomalies. Total REE contents and light (LREE)/heavy (HREE) ratios increased from the Early to Middle Permian. Observed variations in initial Sr, Nd, and Pb isotopes (⁸⁷Sr/⁸⁶Sr_i = 0.7013–0.7066, ²⁰⁷Pb/²⁰⁴Pb_i = 15.53–15.63, and ²⁰⁸Pb/²⁰⁴Pb_i = 38.04–38.64 for a given ²⁰⁶Pb/²⁰⁴Pb_i; εNd = +0.69 to ?11.55) can be explained by crustal interaction with mantle sources, as is characteristic of metasomatism by slab‐derived fluids or assimilation and fractional crystallization (AFC) processes during magmatic evolution. The observed geochemical signatures, coupled with stratigraphic constraints, support the hypothesis that an initial arc formed during the Permian due to southward subduction of the Paleotethys, predating the well‐known Mesozoic arc preserved in the Gangdise Terrane.     

Apatite/liquid partition coefficients for the rare earth elements and strontium

Sixteen sets of apatite/liquid partition coefficients (D^ap/liq) for the rare earth elements (REE; La, Sm, Dy, Lu) and six values for Sr were experimentally determined in natural systems ranging from basanite to granite. The apatite + melt (glass) assemblages were obtained from starting glasses artificially enriched in REE, Sr and fluorapatite components; these were run under dry and hydrous conditions of 7.5–20 kbar and 950–1120°C in a solid-media, piston-cylinder apparatus. An SEM-equipped electron microprobe was used for subsequent measurement of REE and Sr concentrations in coexisting apatites and quenched glasses. The resulting partition coefficient patterns resemble previously determined apatite phenocryst/groundmass concentration ratios in the following respects: (1) the rare earth patterns are uniformly concave downward (i.e., the middle REE are more compatible in apatite than the light and heavy REE); (2) D_REE^ap/liq is much higher for silicic melts than for basic ones; and (3) strontium (and therefore Eu²⁺) is less concentrated by apatite than are the trivalent REE. The effects of both temperature and melt composition on D_REE^ap/liq are systematic and pronounced. At 950°C, for example, a change in melt SiO₂ content from 50 to 68 wt.% causes the average REE partition coefficient to increase from ～7 to ～30. A 130°C increase in temperature, on the other hand, results in a two-fold decrease in D_REE^ap/liq. Partitioning of Sr is insenstitive to changes in melt composition and temperature, and neither the Sr nor the REE partition coefficients appear to be affected by variations in pressure or H₂O content of the melt.The experimentally determined partition coefficients can be used not only in trace element modelling, but also to distinguish apatite phenocrysts from xenocrysts in rocks. Reported apatite megacryst/host basalt REE concentration ratios [12], for example, are considerably higher than the equilibrium partition coefficients, which suggest that in this particular case the apatite is actually xenocrystic.A reversal experiment incorporated in our study yielded diffusion profiles of REE in apatite, from which we extracted a REEαCa interdiffusion coefficient of 2–4×10^?14 cm²/s at 1120°C. Extrapolated downward to crustal temperatures, this low value suggests that complete REE equilibrium between felsic partial melts and residual apatite is rarely established.     

Early Oligocene alkaline lamprophyric dykes from the Jandaq area (Isfahan Province,Central Iran): Evidence of Central–East Iranian microcontinent confining oceanic crust subduction

The Jandaq lamprophyres occur as eight mostly parallel dykes, which cross‐cut Eocene volcanic and sedimentary rocks of the Pis‐Kuh Formation in dominant north to south direction. These lamprophyres are mainly composed of kaersutite, clinopyroxene, olivine, feldspar, ilmenite, and spinel as primary minerals. The rocks studied here are enriched in alkalis, TiO₂, large ion lithophile elements, and light rare‐earth elements (LREE), with SiO₂ content between 41.7 and 46.2 wt%, and are classified as camptonite and alkaline lamprophyre according to the mineralogical and chemical characteristics. These rocks exhibit positive Eu anomalies (Eu/Eu* = 1.08–1.39) and are characterized by strong enrichment in LREE relative to heavy REEs, and also by varied Zr/Hf ratios. The geochemical features of the rocks suggest that the lamprophyre magmas were derived from low‐degree melting of an amphibole garnet lherzolite that experienced strong metasomatism by carbonate‐rich fluids in response to dehydration melting from the subducted slab. The Jandaq lamprophyric magmatism has been attributed to the former subduction of the Central–East Iranian microcontinent confining oceanic crust from the Triassic to Eocene, and decompression melting induced by the extensional basin of the Jandaq area in the early Oligocene.     

Geochemistry, K–Ar geochronology and Sr–Nd–Pb isotope compositions of pitchstone in Gohado, southwestern Okcheon Belt, South Korea

Abstract Geochemical and Sr–Nd–Pb isotope characteristics, as well as K–Ar geochronology of a massive pitchstone (volcanic glass) stock erupted into Late Cretaceous lapilli tuff and rhyolite in the Gohado area, southwestern Okcheon Belt, South Korea, are reported. The pitchstones are highly evolved with SiO₂ contents ranging from ～72 to 73 wt%, K₂O/Na₂O ratios of 1.04–1.23 and low MgO/FeO^t values (0.17–0.20). The pitchstones are weakly peraluminous and the ASI (molar Al₂O₃/Na₂O + K₂O + CaO) values are significantly lower than 1.1. The pitchstones also display a general calc‐alkaline nature with significant alkali contents. The rare earth elements (REE) compositions show moderately fractionated nature with (La/Yb)_N ranging from 11 to 16. Chondrite normalized REE patterns show relative enrichment of light REE over heavy REE and moderate Eu anomaly (Eu/Eu* ratio varies from 0.53 to 0.57). A distinct negative Nb anomaly is observed for all pitchstones on a primitive mantle normalized trace element diagram, typical of subduction‐related magmatism and crustal‐derived granites. All these features are characteristic of I‐type granites derived from a continental arc. The pitchstones have Zr contents of 98.5–103.5 ppm with zircon thermometry yielding temperatures of 749–755°C (mean 752°C). The K–Ar analyses of representative pitchstone samples yielded ages of 58.7 ± 2.3 and 62.4 ± 2.1 Ma with a mean age of 61 Ma. The rocks show nearly uniform initial ⁸⁷Sr/⁸⁶Sr isotopic ratios of 0.7104–0.7106 and identical ¹⁴³Nd/¹⁴⁴Nd initial ratio of 0.5120. The rocks display negative εNd (61 Ma) values of ?12. The depleted mantle model ages (T_DM) range from 1.54 Ga to 1.57 Ga. The Pb isotope ratios are ²⁰⁶Pb/²⁰⁴Pb = 18.522–18.552, ²⁰⁷Pb/²⁰⁴Pb = 15.642–15.680 and ²⁰⁸Pb/²⁰⁴Pb = 38.794–38.923. These ratios suggest that the Gohado pitchstones were formed in a continental arc environment by partial melting of a 1.54 Ga to 1.57 Ga parental sources of lower crustal rocks probably of mafic or intermediate compositions.     

Rare-earth element (REE) behaviour in the alteration facies of the active magmatic–hydrothermal system of Vulcano (Aeolian Islands,Italy)

This work reports a study on the rare-earth element (REE) behaviour in the high-sulfidation-type superficial alteration and in the phyllic and propylitic alteration in the subsurface of the island of Vulcano. The results of this study demonstrate notable differences in the REE behaviour in the different alteration facies. In silicic alteration, all REE are equally strongly depleted; in advanced argillic alteration, LREE are quite immobile whereas HREE are strongly depleted; in intermediate argillic, phyllic and propylitic alteration, REE patterns are almost unchanged compared with their fresh rock equivalents. These features indicate that the behaviour of REE in hydrothermal alteration facies at La Fossa is mainly controlled by pH, availability of complexing ions in the fluid (mainly SO₄²⁻ and, in the silicic facies, F⁻) and the presence of secondary minerals able to host REE in their structures. The origin of the acid fluids is related to the hypogenic introduction of prevalently magmatic acid gases produced by the degassing of the shallow magmatic system of La Fossa volcano. In the active high-temperature fumarolic field of La Fossa, REE behaviour illustrates the transition from a dry vapor system, corresponding to the high-temperature fumaroles, to a wet condensing system in the surrounding area. The results of this research, carried out on an active high-sulfidation system, provide a useful tool for the study of high-sulfidation epithermal ore deposits and particularly help to understand the alteration processes during the main stage of hypogene wall rock alteration.     

Plagioclase picrites in the Kamchatsky Mys Peninsula,Eastern Kamchatka

The zone of serpentinite melange in the Kamchatsky Mys Peninsula was found to contain high-magnesium ultramafic volcanic rocks, viz., plagioclase picrite (oceanite) with a MgO concentration of 22.5–25.8%. We evaluated the petrochemical and geochemical characteristics of these rocks, as well as their mineral compositions. The olivine phenocrysts make up 50–60% of the rock volume; their composition (mostly 87–89 mol % Fo) and the composition of melt inclusions in them indicate their origin from a picritic melt with an additional cumulative enrichment in olivine. The geochemical parameters (Zr/Y = 3.1, Th/Yb = 0.14–0.18, Nb/Yb = 2.39–2.66, La_(N)/Sm_(N) = 1.0–1.1, La_(N)/Yb_(N) = 1.24–1.42) indicate an oceanic genesis of these rocks affected by a mantle plume.     

Late Permian post‐ophiolitic trondhjemites from Central Iran: a mark of subduction role in growth of Paleozoic continental crust

Late Permian trondhjemites in the Anarak area occur as stocks and dykes, which cross cut the Anarak ophiolite and its overlying metasedimentary rocks, and are exposed along the northern Anarak east–west main faults. These leucocratic intrusive bodies have enclaves of all ophiolitic units and metamorphic rocks. They are composed of amphibole, plagioclase (oligoclase), quartz, zircon and muscovite. Secondary minerals are chlorite (pycnochlorite), epidote, albite, magnetite and calcite. Whole‐rock major‐ and trace‐element analyses reveal that they are characterized by high SiO ₂ (67.8–71.0 wt%), Al ₂ O ₃ (14.9–17.1 wt%) and Na ₂ O (5.3–8.6 wt%), low K ₂ O (0.1–1.5 wt%; average: 0.8 wt%), low Rb/Sr ratio (0.01–0.40; average: 0.09), low Y (3–6 ppm), negative Ti, Nb and Ta anomalies, slightly negative or positive Eu anomaly, LREE enrichment and fractionated HREE. These rocks present 2 to 40 times enrichment in inclined chondrite‐normalized REE patterns. Geochemical characteristics of the Anarak trondhjemites all reflect melting of a mafic protolith at more than 10 kbar. The field evidence and whole‐rock chemistry reveal that these rocks have been crystallized from magmas derived from melting of subducted Anarak oceanic crust. This study reveals that melting of garnet amphibolite was an important element of continent formation in the study area.     

Geochemical characteristics of Cretaceous basaltic rocks in South China and constraints on Pacific plate subduction

The South China, including Yangzi Craton and the Cathaysian Block, belongs to the southern part of East Asia continent. It borders Pacific plate on the east side and Qinling-Dabie Orogen on the north side. During the middle-late Cretaceous, a number of downfaulted red basins (the terrestrial sedimentary basins in Fig. 1) and volcanic- sedimentary basins had been developed in South China[1,2], in which the con-temporaneous basaltic rocks were generally distributed (Fig. 1). Although the …     

Using <Emphasis Type="Italic">in situ</Emphasis> REE analysis to study the origin and diagenesis of dolomite of Lower Paleozoic,Tarim Basin

In situ REE concentrations of various dolomites from Tarim Basin were obtained by LA-ICP-MS analysis, and the data were normalized to standard seawater (Seawater Normalized=SWN). Most of the samples have a ΣREE range of less than 20 ppm. All samples show similar REE_SWN distributions with heavy REE depletion, and positive Ce anomaly, which indicates that they have the same dolomitization fluids (seawater). According to the origin and diagenetic process of dolomite, two types of dolomite are determined and described as follows: 1) syndepositional dolomite, with the highest REE concentrations (more than 20 ppm), the cores of which are more enriched in REE compared with their cortexes, indicating that they underwent the dolomitization of calcareous sediments by hypersaline and subsequent diagenesis decreased the REE content of the cortex because of the low REE concentration of the diagenetic fluids; 2) diagenetic dolomite, which can be subdivided into four groups. (1) burial dolomite which has higher REE concentrations than limestone, but lower than syndepositional dolomite. This shows that pore fluids with high salinity dolomitized the pre-existing limestone; (2) void filling dolomite which has the similar REE patterns with the matrix dolomite. In addition, the Eu anomaly is not obvious, suggesting that the dolomitization fluids originated from the diagenetic fluids; (3) recrystallized dolomite, whose REE concentration was obviously decreased, indicating that the REE concentration was decreased during the recrystallization processes; and (4) hydrothermal altered void-filling dolomite, which has the lowest REE concentration, but obvious positive Eu anomaly, reflecting its hydrothermal activity related origin. Thus, the diverse REE signatures, which were recorded in different dolomites, retain the information of their formation conditions and subsequent diagenetic processes. In situ REE analysis of dolomite is an effective probe into the origin and diagenetic process of dolomite. Supported by National Basic Research Program of China (Grant No. 2005CB422103)     

Geochemistry of I-type granitoids in the Karaburun Peninsula, West Turkey: Evidence for Triassic continental arc magmatism following closure of the Palaeotethys

Abstract Triassic granitoids related to Palaeo- and Neo-Tethyan events occur widely in the metamorphic terranes largely affected by the Alpine orogeny. A first recorded unmetamorphosed plutonic body intruded into the Palaeotethyan mélange in western Turkey, called the Karaburun granodiorite, is composed of two small intrusive stocks that were emplaced between 240 and 220 Ma. It is compositionally diverse, ranging from granodiorite and tonalite to diorite. These rocks show heterogeneous compositions with 54 to 65 wt % SiO₂ and are calc-alkaline in character. They are also subalkaline with molar ratios of Al₂O₃/(Na₂O + K₂O) from 0.74 to 1.00 and are metaluminous. Most samples are diopside-normative (0.36–8.64), with Na₂O > K₂O. Chondrite normalized rare earth element (REE) patterns show various degrees of light REE (LREE) enrichment, with La _N = 57.79 to 99.59 and (La/Yb) _N = 5.98–7.85 and Eu negative anomalies (Eu/Eu* = 0.62–0.86). These rocks have coherent patterns in ocean ridge granite (ORG) normalized trace-element plots, marked by variable enrichment in K, Rb, Ba, Th, Ce and depletion in Ta and Nb, similar to I-type granites from subduction zones. In primitive mantle-normalized multi element variation diagrams, the granodiorites show pronounced depletions in the high-field-strength elements (HFSE; Nb, Ta, Zr), Sr, P, and Ti. Trace-element modeling of the Karaburun granodiorite suggests an origin through partial melting of the subduction-modified mantle wedge with minor contribution of crustal components through a process of strong fractional crystallization (FC) combined with slight assimilation-fractional crystallization (AFC). Exposures of typical continental-arc granodiorites in the Karaburun Mélange support the validity of the subduction-accretion model that implies the presence of an active continental margin following closure of the Palaeotethyan Ocean during the Triassic.