Trace element distribution among rock-forming minerals from metamorphosed to partially molten basic igneous rocks in a contact aureole (Fuerteventura, Canaries)

Low pressure partial melting of basanitic and ankaramitic dykes gave rise to unusual, zebra-like migmatites, in the contact aureole of a layered pyroxenite–gabbro intrusion, in the root zone of an ocean island (Basal Complex, Fuerteventura, Canary Islands). These migmatites are characterised by a dense network of closely spaced, millimetre-wide leucocratic segregations. Their mineralogy consists of plagioclase (An_32–36), diopside, biotite, oxides (magnetite, ilmenite), +/− amphibole, dominated by plagioclase in the leucosome and diopside in the melanosome. The melanosome is almost completely recrystallised, with the preservation of large, relict igneous diopside phenocrysts in dyke centres. Comparison of whole-rock and mineral major- and trace-element data allowed us to assess the redistribution of elements between different mineral phases and generations during contact metamorphism and partial melting.

Dykes within and outside the thermal aureole behaved like closed chemical systems. Nevertheless, Zr, Hf, Y and REEs were internally redistributed, as deduced by comparing the trace element contents of the various diopside generations. Neocrystallised diopside – in the melanosome, leucosome and as epitaxial phenocryst rims – from the migmatite zone, are all enriched in Zr, Hf, Y and REEs compared to relict phenocrysts. This has been assigned to the liberation of trace elements on the breakdown of enriched primary minerals, kaersutite and sphene, on entering the thermal aureole. Major and trace element compositions of minerals in migmatite melanosomes and leucosomes are almost identical, pointing to a syn- or post-solidus reequilibration on the cooling of the migmatite terrain i.e. mineral–melt equilibria were reset to mineral–mineral equilibria.     

Crustal contamination and fluid/rock interaction in the carbonatites of Fuerteventura (Canary Islands, Spain): a C, O, H isotope study

Fuerteventura—the second largest of the Canary Islands consists of Mesozoic sediments, submarine volcanic rocks, dike swarms and plutons of the Basal Complex, and younger subaerial basaltic and trachytic series. Carbonatites are found in two Basal Complex exposures: the Betancuria Massif in the central part of the island and the Esquinzo area in the north. values of the carbonatites increase progressively from south to north of the island. This phenomenon is attributed to different degrees of assimilation of sedimentary carbonate. Homogeneous, typically magmatic values for carbonatites which have preserved primary igneous textures and minerals suggest a well-mixed reservoir where changes in values result from the storage of carbonate magmas at different structural levels. The magma storage allowed assimilation of sediment to varying degrees before final emplacement of carbonatites. Shifts in towards more positive and negative values from presumed primary compositions are observed in the carbonatites. On the basis of the oxygen isotope compositions of calcite, mica and K-feldspar, and the hydrogen isotope compositions of micas, the changes in the values of the carbonatites can be related to fluid/rock interactions.     

Oxygen isotope geochemistry of the Omeo Metamorphic Complex,Victoria: Implications for metamorphic fluid flow,mineralisation and anatexis

Metamorphosed turbidites from the Omeo Metamorphic Complex show only minor changes in δ¹⁸O values with increasing metamorphic grade from 13.4 ± 1.7% in the chlorite and biotite zones to 12.3 ± 1.0% in the sillimanite + K‐feldspar zone. Rocks within 5 km of the S‐type granite at Hume Dam have δ¹⁸O values of 6.8–8.1% that probably reflect interaction with heated meteoric‐igneous fluids. Interaction with igneous fluids has also occurred close to other I‐ and S‐type granites in this region. However, pervasive metamorphic fluid‐rock interaction in this terrain did not occur, which limits the region's potential for hydrothermal mineralisation. Anatexis at high grades was probably via dehydration‐melting reactions that consumed muscovite and biotite, which is consistent with there being little fluid present during metamorphism. Small (kilometre scale or less) S‐type granites in the sillimanite + K‐feldspar zone have δ¹⁸O values similar to those of the surrounding metasediments and probably formed by melting of those rocks. By contrast, larger (tens of kilometres scale) Ca‐rich, peraluminous, S‐type granites have lower δ¹⁸O values than the surrounding metasediments, and may represent melts of underlying middle to lower crust.     

Using a genetic algorithm for 3-D inversion of gravity data in Fuerteventura (Canary Islands)

The use of genetic algorithms in geophysical inverse problems is a relatively recent development and offers many advantages in dealing with the non-linearity inherent in such applications. We have implemented a genetic algorithm to efficiently invert a set of gravity data. Employing several fixed density contrasts, this algorithm determines the geometry of the sources of the anomaly gravity field in a 3-D context. The genetic algorithms, based on Darwins theory of evolution, seek the optimum solution from an initial population of models, working with a set of parameters by means of modifications in successive iterations or generations. This searching method traditionally consists of three operators (selection, crossover and mutation) acting on each generation, but we have added a further one, which smoothes the obtained models. In this way, we have designed an efficient inversion gravity method, confirmed by both a synthetic example and a real data set from the island of Fuerteventura. In the latter case, we identify crustal structures related to the origin and evolution of the island. The results show a clear correlation between the sources of gravity field in the model and the three volcanic complexes recognized in Fuerteventura by other geological studies.     

Tracking meteoric infiltration into a magmatic-hydrothermal system: A cathodoluminescence, oxygen isotope and trace element study of quartz from Mt. Leyshon, Australia

The oxygen isotope and trace element composition of hydrothermal quartz has been integrated with scanning electron microscope-cathodoluminescence (SEM-CL) images and fluid inclusion properties to track fluid sources and hydrothermal processes in the Mt. Leyshon Au deposit, Australia. Oxygen isotope and trace element data were collected on parallel traverses across the same quartz sections, using secondary isotope mass spectrometry (SIMS) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), respectively, with SEM-CL images obtained before analysis for petrographic context. Over the 280 to 650 °C quartz precipitation range suggested by fluid inclusion microthermometry, δ¹⁸O_quartz varies from 0.0 to 14.4‰, corresponding to a wide range of equilibrium δ¹⁸O_fluid values, from-6.1 to 10.2‰ (vs. V-SMOW). The δ¹⁸O_quartz signature varies systematically among distinct SEM-CL quartz generations (both within and between samples), and can be correlated with variations in temperature and fluid composition, but is independent of intra-generational oscillatory zoning. In contrast, Al and Li concentrations correlate broadly with CL intensity in oscillatory quartz, whereas their concentration is unpredictable in sealed fractures and overgrowths. Concentrations of B, Mg, Na, P, Cl, K, Ti, Mn, Fe, Ge, and Sn are independent of Al, Li, and oscillatory CL features, but Ti correlates with quartz precipitation temperature. Although no systematic correlation between δ¹⁸O_quartz and trace element concentrations was found, complementary patterns exist in narrow overgrowths of low δ¹⁸O_quartz ( 0‰) and high Al (> 10,000 ppma). These quartz zones likely formed during the incursion of ¹⁸O-depleted meteoric water into the magmatically-dominated Mt. Leyshon hydrothermal system. We interpret the highest Al concentrations as the result of high quartz precipitation rates, triggered by depressurisation of the hydrothermal cell. The decoupling of oxygen isotope and trace element patterns in quartz leads to the suggestion that (1) under most circumstances, temperature and fluid chemistry dominate δ¹⁸O_quartz, and (2) the trace element record, and in particular Al and Li, is influenced by the superimposed effects of quartz precipitation rate.     

Interrelations between coeval mafic and A-type silicic magmas from composite dykes in a bimodal suite of southern Israel, northernmost Arabian–Nubian Shield: Geochemical and isotope constraints

Late Neoproterozoic bimodal dyke suites are abundant in the Arabian–Nubian Shield. In southern Israel this suite includes dominant alkaline quartz porphyry dykes, rare mafic dykes, and numerous composite dykes with felsic interiors and mafic margins. The quartz porphyry chemically corresponds to A-type granite. Composite dykes with either abrupt or gradational contacts between the felsic and mafic rocks bear field, petrographic and chemical evidence for coexistence and mixing of basaltic and rhyolitic magmas. Mixing and formation of hybrid intermediate magmas commenced at depth and continued during emplacement of the dykes. Oxygen isotope ratios of alkali feldspar in quartz porphyry (13 to 15‰) and of plagioclase in trachydolerite (10–11‰) are much higher than their initial magmatic ratios predicted by equilibrium with unaltered quartz (8 to 9‰) and clinopyroxene (5.8‰). The elevation of δ¹⁸O in alkali feldspar and plagioclase, and extensive turbidization and sericitization call for post-magmatic low-temperature (≤ 100 °C) water–rock interaction. Hydrous alteration of alkali feldspar, the major carrier of Rb and Sr in the quartz–porphyry, also accounts for the highly variable and unusually high I(Sr) of 0.71253 to 0.73648.

The initial ¹⁴³Nd/¹⁴⁴Nd ratios, expressed by ε_Nd(T) values, are probably unaltered and show small variation in mafic and felsic rocks within a narrow range from + 1.4 to + 3.3. The Nd isotope signature suggests either a common mantle source for the mafic and silicic magmas or a juvenile crustal source for the felsic rocks (metamorphic rocks from the Elat area). However, oxygen isotope ratios of zircon in quartz porphyry [δ¹⁸O(Zrn) = 6.5 to 7.2‰] reveal significant crustal contribution to the rhyolite magma, suggesting that mafic and A-type silicic magmas are not co-genetic, although coeval. Comparison of ¹⁸O/¹⁶O ratios in zircon allows to distinguish two groups of A-type granites in the region: those with mantle-derived source, δ¹⁸O(Zrn) ranging from 5.5 to 5.8‰ (Timna and Katharina granitoids) and those with major contribution of the modified juvenile crustal component, δ¹⁸O(Zrn) varying from 6.5 to 7.2‰ (Elat quartz porphyry dykes and the Yehoshafat alkaline granite). This suggests that A-type silicic magmas in the northern ANS originated by alternative processes almost coevally.     

Fluid sources for the La Guitarra epithermal deposit (Temascaltepec district, Mexico): Volatile and helium isotope analyses in fluid inclusions

The La Guitarra deposit (Temascaltepec district, South-Central Mexico), belongs to the low/intermediate sulfidation epithermal type, has a polymetallic character although it is currently being mined for Ag and Au. The mineralization shows a polyphasic character and formed through several stages and sub-stages (named I, IIA, IIB, IIC, IID, and III). The previous structural, mineralogical, fluid inclusion and stable isotope studies were used to constrain the selection of samples for volatile and helium isotope analyses portrayed in this study. The N₂/Ar overall range obtained from analytical runs on fluid inclusion volatiles, by means of Quadrupole Mass Spectrometry (QMS), is 0 to 2526, and it ranges 0 to 2526 for stage I, 0 to 1264 for stage IIA, 0 to 1369 for stage IIB, 11 to 2401 for stage IIC, 19 to 324 for stage IID, and 0 to 2526 for stage III. These values, combined with the CO₂/CH₄ ratios, and N₂-He-Ar and N₂-CH₄-Ar relationships, suggest the occurrence of fluids from magmatic, crustal, and shallow meteoric sources in the forming epithermal vein deposit. The helium isotope analyses, obtained by means of Noble Gas Mass Spectrometry, display R/Ra average values between 0.5 and 2, pointing to the occurrence of mantle-derived helium that was relatively diluted or “contaminated” by crustal helium. These volatile analyses, when correlated with the stable isotope data from previous works and He isotope data, show the same distribution of data concerning sources for mineralizing fluids, especially those corresponding to magmatic and crustal sources. Thus, the overall geochemical data from mineralizing fluids are revealed as intrinsically consistent when compared to each other.The three main sources for mineralizing fluids (magmatic, and both deep and shallow meteoric fluids) are accountable at any scale, from stages of mineralization down to specific mineral associations. The volatile and helium isotope data obtained in this paper suggest that the precious metal-bearing mineral associations formed after hydrothermal pulses of predominantly oxidized magmatic fluids, and thus it is likely that precious metals were carried by fluids with such origin. Minerals from base-metal sulfide associations record both crustal and magmatic sources for mineralizing fluids, thus suggesting that base metals could be derived from deep leaching of crustal rocks. At the La Guitarra epithermal deposit there is no evidence for an evolution of mineralizing fluids towards any dominant source. Rather than that, volatile analyses in fluid inclusions suggest that this deposit formed as a pulsing hydrothermal system where each pulse or set of pulses accounts for different compositions of mineralizing fluids.The positive correlation between the relative content of magmatic fluids (high N₂/Ar ratios) and H₂S suggests that the necessary sulfur to carry mostly gold as bisulfide complexes came essentially from magmatic sources. Chlorine necessary to carry silver and base metals was found to be abundant in inclusion fluids and although there is no evidence about its source, it is plausible that it may come from magmatic sources as well.     

Stable isotopic evidence for fluid infiltration during contact metamorphism in a multiply-metamorphosed terrane: the Reynolds Range, Arunta Block, central Australia

The Lander Rock Beds form the local basement of the Reynolds Range in the Arunta Inlier of central Australia. These dominantly quartzose and pelitic lithologies underwent low-grade ( c.   400  °C) regional metamorphism prior to contact metamorphism ( c.   2.5  kbar) around S-type megacrystic granitoids at 1820–1800  Ma. The Lander Rock Beds are overlain by metasediments of the Reynolds Range Group, which were subsequently intruded by granitoids at c. 1780  Ma. Regional metamorphism at 1590–1580  Ma produced grades varying from greenschist (400  °C at 4–5  kbar) to granulite (750–800  °C at 4–5  kbar) from north-west to south-east along the length of the Reynolds Range. Oxygen isotope ratios of the Lander Rock Beds were reset from 13.4±0.8 to as low as 6.7 adjacent to the contacts of the larger plutons, and to 10.3±1.1 around the smaller plutons. Biotite in all the major rock types found in the aureoles has δD values between −52 and −69, probably reflecting resetting by a cooling igneous+metamorphic fluid near the plutons. Sapphirine-bearing and other Mg- and Al-rich rock types have low δ¹⁸O values (4.0±0.7). The precursors to these rocks were probably low-temperature ( c. 200  °C) diagenetic–hydrothermal deposits of Mg-rich chlorite, analogous to those in Proterozoic stratiform precious metal and uranium deposits that form by the infiltration of basin brines or seawater. As in the overlying Reynolds Range Group, regional metamorphism involved little fluid–rock interaction and isotopic resetting.     

Geochemical,and stable and radiogenic isotope records in Devonian and Early Carboniferous carbonates from Valle de Tena,central Pyrenees (Spain): evidence for their diagenetic environments

Mineralogical, textural and geochemical investigations were made to determine the post-depositional evolution of Devonian and Early Carboniferous carbonates from Valle de Tena. The carbonate association is made up of low-Mg calcite, which occurs as micrite, spar cements, neomorphic patches and spar filling veinlets. Non-stoichiometric dolomite and ankerite occur as cements (dolomite also as replacements) in the Middle Devonian, post-dating calcite types. All these phases pre-date tectonic stylolites, indicating compaction after stabilization of the carbonate minerals. Strontium concentrations indicate that Early Devonian and Early Carboniferous micrites initially precipitated as aragonite; Middle and Late Devonian micrites precipitated as high-Mg calcites. Both precursors were diagenetically stabilized to low-Mg calcites through interaction with meteoric waters in phreatic environments. Trace elements in dolomite and ankerite indicate precipitation from Sr-enriched meteoric water. All studied carbonates, except Middle Devonian limestones, precipitated in reducing environments, which favoured incorporation of Fe and Mn. Late calcite generations precipitated from more saline waters than micrites. Light ¹⁸O values in micrites suggest alteration mainly in meteoric-phreatic environments. The dolomites and ankerites precipitated from more ¹⁸O-depleted fluids than the calcites, suggesting a greater contribution from meteoric waters. Variations in ¹³C of micrites represent primary secular trends, according to published ¹³C variations. The ¹³C oscillations within each succession probably relate to sea-level oscillations. Strontium isotopes also point to a meteoric origin of diagenetic fluids. Model calculations suggest that O and Sr isotopes equilibrated between calcites and fluid at relatively low water/rock ratios, whereas C isotopic signatures are inherited from limestones.     

Trace element and isotopic (Sr, Nd, Pb, O) arguments for a mid-crustal origin of Pan-African garnet-bearing S-type granites from the Damara orogen (Namibia)

Geochronological data, major and trace element abundances, Nd and Sr isotope ratios, δ¹⁸O whole rock values and Pb isotope ratios from leached feldspars are presented for garnet-bearing granites (locality at Oetmoed and outcrop 10 km north of Omaruru) from the Damara Belt (Namibia). For the granites from outcrop 10 km N′ Omaruru, reversely discordant U–Pb monazite data give ²⁰⁷Pb/²³⁵U ages of 511±2 Ma and 517±2 Ma, similar to previously published estimates for the time of regional high grade metamorphism in the Central Zone. Based on textural and compositional variations, garnets from these granites are inferred to be refractory residues from partial melting in the deep crust. Because P–T estimates from these xenocrystic garnets are significantly higher (800°C/9–10 kbar) than regional estimates (700°C/5 kbar), the monazite ages are interpreted to date the peak of regional metamorphism in the source of the granites. Sm–Nd garnet–whole rock ages are between 500 and 490 Ma indicating the age of extraction of the granites from their deep crustal sources. For the granites from Oetmoed, both Sm–Nd and Pb–Pb ages obtained on igneous garnets range from 500 to 490 Ma. These ages are interpreted as emplacement ages and are significantly younger than the previously proposed age of 520 Ma for these granites based on Rb/Sr whole rock age determinations. Major and trace element compositions indicate that the granites are moderately to strongly peraluminous S-type granites. High initial ⁸⁷Sr/⁸⁶Sr ratios (>0.716), high δ¹⁸O values of >13.8‰, negative initial _Nd values between −4 and −7 and evolved Pb isotope ratios indicate formation of the granites by anatexis of mid-crustal rocks similar to the exposed metapelites into which they intruded. The large range of Pb isotope ratios and the lack of correlation between Pb isotope ratios and Nd and Sr isotope ratios indicate heterogeneity of the involved crustal rocks. Evidence for the involvement of isotopically highly evolved lower crust is scarce and the influence of a depleted mantle component is unlikely. The crustal heating events that produced these granites might have been caused by crustal thickening and thrusting of crustal sheets enriched in heat-producing elements. Very limited fluxing of volatiles from underthrust low- to medium-grade metasedimentary rocks may have also been a factor in promoting partial melting. Furthermore, delamination of the lithospheric mantle and uprise of hot mantle could have caused localized high-T regions. The presence of coeval A-type granites at Oetmoed that have been derived at least in part from a mantle source supports this model.     

Using dual-isotope data to trace the origin and processes of dissolved sulphate: a case study in Calders stream (Llobregat basin,Spain)

Whereas most of the reported δ³⁴S values of dissolved sulphate are positive in the Llobregat basin, Calders stream, which is a tributary of the Llobregat River, is characterised by negative values. Stream waters, sampled monthly between 1997 and 1998, and quarterly in 1999, show an overall increase in δ³⁴S from −10‰ to 0‰, coupled with an increase in Na and Cl concentration. On the other hand, the oxygen isotopic composition of dissolved sulphate, δ¹⁸O, displayed an opposite trend with a slight decrease, from +9‰ to +6‰. Detailed sampling up stream in November 2000 indicated that, contrary to most of the surficial waters of the Llobregat basin with a δ³⁴S_SO4 mainly controlled by evaporites, in Calders stream, sulphate is derived from pyrite oxidation. The dual-isotope approach, coupled with chemical data, allowed us to identify the contribution of ³⁴S-rich sulphate effluents from anthropogenic sources, while mixing models, calculated between natural and anthropogenic sources, enabled us to estimate their contribution. Sudden increases of δ³⁴S and δ¹⁸O of dissolved sulphate in stream waters are believed to be caused by a sulphate reduction process related to oil spillage. The long-term enrichment in δ³⁴S, coupled with a decrease in δ¹⁸O_SO4, from Jan-97 to Aug-99, is interpreted as a progressive increase in the contribution of pig manure.     

Recycled oceanic crust as a source for tonalite intrusions in the mantle section of the Khor Fakkan block,Semail ophiolite (UAE)

Several types of felsic granitoid rocks have been recognized, intrusive in both the mantle and the crustal sequence of the Semail ophiolite. Several models have been proposed for the source of this suite of tonalites, granodiorites, trondhjemites intrusions, however their genesis is still not clearly understood. The sampled Dadnah tonalites that intruded in the mantle section of the Semail ophiolite display arc-type geochemical characteristics, are high siliceous, low-potassic, metaluminous to weakly peraluminous, enriched in LILE, show positive peaks for Ba, Pb, Eu, negative troughs for U, Ti and occur with low δ¹⁸O_H2O, moderate ε_Sr and negative ε_Nd values. They have crystallized at temperatures that range from ∼550 °C to ∼720 °C and pressure ranging from 4.4 kbar to 6.5 kbar. The isotopic ages from our tonalite samples range between 98.6 Ma and 94.9 Ma, slightly older and overlapping with the age of the metamorphic sole. Our field observations, mineralogical, petrological, geochemical, isotopic and melt inclusion data suggest that the Dadnah tonalites formed by partial melting (∼10%–15% continuous or ∼12% batch partial melting), accumulation of plagioclase, fractional crystallization (∼55%–57%), and interaction with their host harzburgites. These tonalites were the end result of partial melting and subsequent contamination and mixing of ∼4% oceanic sediments with ∼96% oceanic lithosphere from the subducted slab. This MORB-type slab melt composed from ∼97% recycled oceanic crust and ∼3% of the overlying mantle.We suggest that a possible protolith for these tonalites was the basaltic lavas from the subducted oceanic slab that melted during the initial stages of the supra-subduction zone (SSZ), which was forming synchronously to the spreading ridge axis. The tonalite melts mildly modified due to low degree of mixing and interaction with the overlying lithospheric mantle. Subsequently, the Dadnah tonalites emplaced at the upper part of the mantle sequence of the Semail ophiolite and are geochemically distinct from the other mantle intrusive felsic granitoids to the south.     

Thermochemical sulphate reduction in the Upper Devonian Cairn Formation of the Fairholme carbonate complex (South-West Alberta, Canadian Rockies): evidence from fluid inclusions and isotopic data

The Fairholme carbonate complex is part of the extensively dolomitized Upper Devonian carbonate reefs in west-central Alberta. The studied formations contain moulds (up to 10 cm in diameter), which are filled partially with (saddle) dolomite, quartz and calcite cements. These cements precipitated from a mixture of brines that acquired high salinity by dissolution of halite and brines derived from evaporated sea water. The fluids were warm (homogenization temperature of primary fluid inclusions of 76 to 200 °C) and saline (20 to 25 wt% NaCl equivalent) and testify to thermochemical sulphate reduction processes. The latter is deduced from S in solid inclusions, CO₂ and H₂S in volatile-rich aqueous inclusions and depleted δ¹³C values down to −26‰ Vienna Pee Dee Belemnite. High ⁸⁷Sr/⁸⁶Sr values (0·7094 to 0·7110) of the cements also indicate interaction of the fluids with siliciclastic sequences. The thermochemical sulphate reduction-related cements probably formed during early Laramide burial. Another (younger) calcite phase, characterized by depleted δ¹⁸O values (−23·9‰ to −13·9‰ Vienna Pee Dee Belemnite), low Na (27 to 37 p.p.m.) and Sr (39 to 150 p.p.m.) concentrations and non-saline (∼0 wt% NaCl equivalent) fluid inclusions, is attributed to post-Laramide meteoric water.     

As–(Ag) sulphide veins in the Spanish Central System: further evidence for a hydrothermal event of Permian age

The Spanish Central System (SCS) has been subjected to repeated deformation and fluid flow events which have produced both sulphide-bearing and barren vein systems. Although several hydrothermal episodes took place between 300 and 100 Ma, fluid circulation during the Permian was especially important, giving rise to a range of different types of deposits. This study presents a multidisciplinary approach leading to the characterisation of the chemistry and age of the hydrothermal fluids that produced the As–(Ag) mineralised stockwork of Mónica mine (Bustaviejo, Madrid). Fluid inclusion data indicate the presence of two different fluids. An initial ore stage (I) formed from a low- to moderate salinity (3–8 wt.% eq. NaCl) H₂O–NaCl–CO₂–CH₄ fluid, at minimum trapping temperature of 350±15 °C and 0.3 kbar. A second H₂O–NaCl fluid is found in three types of fluid inclusions: a high temperature and low salinity type (340±20 °C; 0.8–3.1 wt.% eq. NaCl) also associated to ore stage I, a moderate temperature and very low salinity type (160–255 °C; 0–1.5 wt.% eq. NaCl) represented in ore stage III, and a very low temperature and hypersaline type (60–70 °C; 30–35 wt.% NaCl), unrelated to the mineralising stages and clearly postdating the previous types. ⁴⁰Ar–³⁹Ar dating on muscovite from the early As–Fe stage (I) has provided an age of 286±4 Ma, synchronous with the late emplacement phases of La Cabrera plutonic massif (288±5 Ma) and with other Permian hydrothermal events like Sn–W skarns and W–(Sn) sulphide veins. δ¹⁸O of water in equilibrium with stage I quartz (5.3–7.7‰), δD of water in equilibrium with coexisting muscovite (−16.0‰ to −2.0‰), and sulphide δ³⁴S (1.5–3.6‰) values are compatible with waters that leached metamorphic rocks. The dominant mechanism of the As–(Ag) deposition was mixing and dilution processes between aqueous–carbonic and aqueous fluids for stage I (As–Fe), and nearly isobaric cooling processes for stages II (Zn–Cu–Sn) and III (Pb–Ag). The origin and hydrothermal evolution of As–(Ag) veins is comparable to other hydrothermal Permian events in the Spanish Central System.     

A mantle-derived bimodal suite in the Hercynian Belt: Nd isotope and trace element evidence for a subduction-related rift origin of the Late Devonian Brévenne metavolcanics, Massif Central (France)

In the Brévenne Series (NE Massif Central), a low-grade bimodal association of metabasalts and metarhyolites is exposed, together with intrusive trondhjemite bodies. Zircon U-Pb dating constrains their magmatic emplacement at 366 ± 5 Ma and 358 ± 1 Ma, respectively. The metabasalts are characterized by a distinct enrichment in incompatible elements (e.g. Th and LREE) and positive ɛNd_i (from +5 to +8). Combined isotope and trace element systematics rule out crustal contamination of mafic melts as a suitable cause of the LILE (large ion lithophile element)-enrichment. Rather, a mixing process between a component similar to mid ocean ridge basalts and an enriched end-member with ɛNd_i > +5 is suggested. An enriched-mantle source of ocean island basalt affinity is precluded by the relative depletion of high field strength elements, especially Nb which shows negative anomalies in chondrite-normalized patterns. On the contrary, a subduction-related origin for the LILE enrichment would be more consistent. It may be inferred that arc-like melts [enriched in Th and LREE (light rare earth elements) and depleted in Nb, with ɛNd_i > +5] were produced through partial melting of a depleted-mantle source, to which a small amount of crustally derived component had been added. The metarhyolites are enriched in LILE, and have a close genetic relationship with the metabasalts, as evidenced by their high ɛNd_i (from +4.7 to +6.8). Although the chemical evidence remains ambiguous, it is suggested that fractional crystallization, accompanied by subordinate assimilation, is the petrogenetic process most consistent with the data. The trondhjemites are isotopically distinct from the metarhyolites. Their ɛNd_i values (from −1.0 to +2.2) reflect an important contribution of continental crust to their genesis, and disprove their inferred cogenetism with the felsic volcanics. A review of modern environments in which such bimodal suites are exposed, shows that settings involving incipient rifting of a volcanic arc fringing a continental margin, or built upon young, thin continental crust might provide suitable analogues. Geodynamic reconstructions are complicated by subsequent tectonic events which disrupted the initial patterns, and by Mesozoic-Cenozoic sedimentary cover. However, this subduction-related magmatism enlarges the growing body of evidence for southward subduction processes until the Late Devonian during the evolution of the northern flank of the European Variscides. As a general implication, it is suggested that the combined use of the Sm-Nd system with incompatible elements relatively resistant during alteration and low-grade metamorphism (REE, Th, Zr, Nb) may provide diagnostic criteria for recognizing the tectonic setting of bimodal metaigneous suites in ancient orogenic belts. Received: 21 April 1997 / Accepted: 30 June 1997     

Lake George revisited: new evidence for the origin and evolution of a large closed lake,Southern Tablelands,NSW, Australia. 2: earliest Pleistocene (Gelasian) environments

The three sedimentary units infilling Lake George provide the longest quasi-continuous sedimentary record of any Australian lake basin. A combination of cosmogenic nuclide burial, magnetostratigraphy and biostratigraphic dating techniques previously has shown that the basal (fluvial) unit, the Gearys Gap Formation, began accumulating at ca 4 Ma, in the early Pliocene (Zanclean), and (ii) deposition had ceased by ca 3 Ma, in the mid-late Pliocene (Piacenzian). The same techniques confirm the middle unit, the (fluvio-lacustrine) Ondyong Point Formation began accumulating in the late Pliocene and deposition continued into the earliest Pleistocene (Gelasian) when a shallow but probably laterally extensive freshwater lake extended across the drillhole site. Our data provide a minimum Gelasian age for tectonic blockage of former spillway(s) and formation of paleo-Lake George. Whether this was the earliest lake to form within the basin is unknown, since the dated intervals are separated by a ferric hardpan, interpreted as representing a prolonged period of erosion or non-deposition. Temperate rainforest angiosperms including Nothofagus growing during the late Pliocene had been extirpated or become extinct during this interval, although a number of gymnosperms, now endemic to New Caledonia, New Guinea, New Zealand and Tasmania still survived in the otherwise sclerophyll-dominated vegetation. The succession of plant communities is considered to be due to effectively drier local conditions, which in turn reflect regional aridification during the Plio-Pleistocene transition, despite the formation of a freshwater lake across the basin. The sequence provides a reliable framework for recognising and correlating Plio-Pleistocene deposits elsewhere on the Southern Highlands.     

Major and trace element geochemistry and isotope (Sr, Nd, Pb, O) systematics of an Archaean basement involved in a 2.0 Ga very high-temperature (1000°C) metamorphic event: In Ouzzal Massif, Hoggar, Algeria

The In Ouzzal granulitic massif is composed mainly of various meta-igneous rocks which, in spite of Rb, U, Th, Cs and some K and Sr mobility, can be dated and generally classified according to their chemical composition as follows. Basic and ultrabasic granulites interlayered with the metasediments correspond to (1) ultrabasic cumulates from dislocated tholeiitic bodies, (2) ancient komatiitic to high-Mg tholeiitic basalts similar to the suites found in Archaean greenstone belts and (3) calcalkaline protoliths of high-K andesitic composition. No geochronological constraints are available apart from the depositional age of some associated sediments which is younger than 2.70 Ga detrital zircons, and the Nd model age of the andesitic granulites of c. 3.4 Ga. In spite of the high-grade metamorphism, the acidic magmatic precursors of the charnockites can be divided in three groups. (1) The most juvenile acid orthogneisses are trondhjemitic or tonalitic in composition, being similar to the TTG suites which are classically considered to be formed by partial melting of mantle-derived protoliths. The 3.3–3.2 Ga T_DM indicates a possible age of separation from the mantle reservoir while the plutons may have been emplaced between 3.3 and 2.7 Ga (U–Pb zircon & Nd ages). (2) A group of alkaline granitic gneisses, similar in composition to rift-related-granites, were emplaced at 2650±10 Ma (U–Pb & Rb–Sr ages) in a thick continental crust. (3) Calcalkaline granodioritic and monzogranitic suites derived from the partial melting of continental precursors (3.5–3.3 Ga), in lower to middle levels of the continental crust. They were emplaced close to 2.5 Ga during crustal thickening. The very high-temperature metamorphism occurred at 2002±7 Ma from the age of synfoliation intrusions and was probably related to major overthrusting. Retrogressive metamorphism is dated at 1.95 Ga from garnet-Nd ages. In spite of the very high-temperature conditions, partial melting during granulite facies metamorphism may be restricted to scarce cordierite-bearing monzogranitic gneisses. The 2.0 Ga VHT metamorphism could be related to overthrusting, extensional or underplating processes.     

Genesis of amethyst geodes in basaltic rocks of the Serra Geral Formation (Ametista do Sul,Rio Grande do Sul,Brazil): a fluid inclusion,REE, oxygen,carbon, and Sr isotope study on basalt,quartz, and calcite

In the Ametista do Sul area, Rio Grande do Sul, Brazil, amethyst-bearing geodes are hosted by a ~40- to 50-m-thick subhorizontal high-Ti basaltic lava flow of the Lower Cretaceous Paraná Continental Flood Basalt Province. The typically spherical cap-shaped, sometimes vertically elongated geodes display an outer rim of celadonite followed inwards by agate and colorless and finally amethystine quartz. Calcite formed throughout the whole crystallization sequence, but most commonly as very late euhedral crystals, sometimes with gypsum, in the central cavity. Fluid inclusions in colorless quartz and amethyst are predominantly monophase and contain an aqueous liquid. Two-phase liquid–vapor inclusions are rare. Some with a consistent degree of fill homogenize into the liquid between 95 and 98 °C. Ice-melting temperatures in the absence of a vapor phase between –4 and +4 °C indicate low salinities. Chondrite-normalized REE patterns of calcites are highly variable and show generally no systematic correlation with the paragenetic sequence. The oxygen isotope composition of calcites is very homogeneous (δ¹⁸O_VSMOW=24.9±1.1‰, n=34) indicating crystallization temperatures of less than 100 °C. Carbon isotope values of calcites show a considerable variation ranging from –18.7 to –2.9‰ (VPDB). The ⁸⁷Sr/⁸⁶Sr ratio of calcites varies between 0.706 and 0.708 and is more radiogenic than that of the host basalt (~0.705). The most likely source of silica, calcium, carbon, and minor elements in the infill of the geodes is the highly reactive interstitial glass of the host basalts leached by gas-poor aqueous solutions of meteoric origin ascending from the locally artesian Botucatú aquifer system in the footwall of the volcanic sequence. The genesis of amethyst geodes in basalts at Ametista do Sul, Brazil, is thus considered as a two-stage process with an early magmatic protogeode formation and a late, low temperature infill of the cavity. Editorial handling: A. Cheilletz     

Slab breakoff: a model for Caledonian, Late Granite syn-collisional magmatism in the orthotectonic (metamorphic) zone of Scotland and Donegal, Ireland

None of the existing models for calc-alkaline “Late Granite” (Siluro–Devonian) genesis in the metamorphic Caledonian orogenic belt of Ireland and Scotland fully explains their spatial, age or chemical character. A consistent model must involve the closure of Iapetus Ocean, where slab breakoff is a natural consequence of attempted subduction of continental crust. Expected outcome is a long linear belt of high-K, calc-alkaline magmas, some with characteristic trace element signatures, specifically high Ba, Sr and Zr. Other features include the critical magmatic association of coeval appinite and granite, rapid uplift, erosion and the low-grade regional metamorphism in the Southern Uplands. The linear heat pulse on breakoff is spatially, intensity and time limited producing small volume melts emplaced as separated plutons, over a short time span. Magmatism in the Caledonian metamorphic belt is accurately accounted for by slab breakoff on collision of Baltica with the Scoto–Greenland margin during the Scandian orogeny, following Iapetus Ocean closure. The two chemically, isotopically and areally distinctive suites in the metamorphic belt in Scotland, viz. the Argyll and Cairngorm Suites, can be modelled by reference to the Donegal granites where sequential partial melting of new, lamprophyric underplated crust, then shallower old crust, as heat conduction moved up through the crust on slab breakoff, produced magmas characteristic of the two suites.