N-MORB crust beneath Fuerteventura in the easternmost part of the Canary Islands: evidence from gabbroic xenoliths

Gabbro xenoliths reported in this paper were collected in northern Fuerteventura, the Canary Island located closest to the coast of Africa. The xenoliths are very fresh and consist of Ti–Al-poor clinopyroxene + plagioclase (An_87–67) + olivine (Fo_72–86) ± orthopyroxene. Clinopyroxene and orthopyroxene are constantly and markedly depleted in light rare earth elements (LREE) relative to heavy REE (HREE), as expected for cumulus minerals formed from highly refractory N-MORB-type melts. In contrast, whole-rock Primordial Mantle-normalized trace element patterns range from mildly S-shaped (mildly depleted in Pr–Sm relative to both the strongly incompatible elements Rb–La and the HREE) to enriched. Estimates show that the trace element compositions of the rocks and their minerals are compatible with formation as N-MORB gabbro cumulates, which have been infiltrated at various extents (≤1% to >5%) by enriched alkali basaltic melts. The enriched material is mainly concentrated along grain boundaries and cracks through mineral grains, suggesting that the infiltration is relatively recent, and is thus associated with the Canary Islands magmatism. Our data contradict the hypothesis that a mantle plume was present in this area during the opening of the Atlantic Ocean. No evidence of continental material that might reflect attenuated continental crust in the area has been found. Gabbro xenoliths with REE and trace element compositions similar to those exhibited by the Fuerteventura gabbros are also found among gabbro xenoliths from the islands of La Palma (western Canary Islands) and Lanzarote. The compositions of the most depleted samples from these islands are closely similar, implying that there was no significant change in chemistry during the early stages of formation of the Atlantic oceanic crust in this area. Strongly depleted gabbros similar to those collected in Fuerteventura have also been retrieved in the MARK area along the central Mid-Atlantic Ridge. The presence of N-MORB oceanic crust beneath Fuerteventura implies that the continent–ocean transition in the Canary Islands area must be relatively sharp, in contrast to the situation both further north along the coast of Morocco, and along the Iberian peninsula.     

Oxygen isotope heterogeneity of the mantle beneath the Canary Islands: insights from olivine phenocrysts

A relatively narrow range of oxygen isotopic ratios (?? ¹⁸O?=?5.0?C5.4??) is preserved in olivine of mantle xenoliths, mid-ocean ridge (MORB), and most ocean island basalts (OIB). The values in excess of this range are generally attributed either to the presence of a recycled component in the Earth??s mantle or to shallow level contamination processes. A viable way forward to trace source heterogeneity is to find a link between chemical (elemental and isotopic) composition of the earlier crystallized mineral phases (olivine) and the composition of their parental magmas, then using them to reconstruct the composition of source region. The Canary hotspot is one of a few that contains ~1- to 2-Ga-old recycled ocean crust that can be traced to the core-mantle boundary using seismic tomography and whose origin is attributed to the mixing of at least three main isotopically distinct mantle components i.e. HIMU, DMM, and EM. This work reports ion microprobe and single crystal laser fluorination oxygen isotope data of 148 olivine grains also analyzed for major and minor elements in the same spot. The olivines are from 20 samples resembling the most primitive shield stage picrite through alkali basalt to basanite series erupted on Gran Canaria, Tenerife, La Gomera, La Palma and El Hierro, Canary Islands, for which shallow level contamination processes were not recognized. A broad range of ?? ¹⁸O_olivine values from 4.6 to 6.1?? was obtained and explained by stable, long-term oxygen isotope heterogeneity of crystal cumulates present under different volcanoes. These cumulates are thought to have crystallized from mantle-derived magmas uncontaminated at crustal depth, representing oxygen isotope heterogeneity of source region. A relationship between Ni?×?FeO/MgO and ?? ¹⁸O_olivine values found in one basanitic lava erupted on El Hierro, the westernmost island of the Canary Archipelago, was used to estimate oxygen isotope compositions of partial melts presumably originated from peridotite (HIMU-type component inherited its radiogenic isotope composition from ancient, ~1 to 2?Ga, recycled ocean crust) and pyroxenite (young, <1?Ga, recycled oceanic crust preserved as eclogite with depleted MORB-type isotopic signature) components of the Canary plume. The model calculations yield 5.2 and 5.9?±?0.3?? for peridotite- and pyroxenite-derived melts, respectively, which appeared to correspond closely to the worldwide HIMU-type OIB and upper limit N-MORB ?? ¹⁸O values. This difference together with the broad range of ?? ¹⁸O variations found in the Canarian olivines cannot be explained by thermodynamic effects of oxygen isotopic fractionation and are believed to represent true variations in the mantle, due to oceanic crust and continental lithosphere recycling.     

Evolution of parental magmas of Miocene shield basalts of Gran Canaria (Canary Islands): constraints from crystal,melt and fluid inclusions in minerals

 Picritic units of the Miocene shield volcanics on Gran Canaria, Canary Islands, contain olivine and clinopyroxene phenocrysts with abundant primary melt, crystal and fluid inclusions. Composition and crystallization conditions of primary magmas in equilibrium with olivine Fo_90-92 were inferred from high-temperature microthermometric quench experiments, low-temperature microthermometry of fluid inclusions and simulation of the reverse path of olivine fractional crystallization based on major element composition of melt inclusions. Primary magmas parental for the Miocene shield basalts range from transitional to alkaline picrites (14.7–19.3 wt% MgO, 43.2–45.7 wt% SiO₂). Crystallization of these primary magmas is believed to have occurred over the temperature range 1490–1150° C at pressures ≈5 kbar producing olivine of Fo_80.6-90.2, high-Ti chrome spinel [Mg/ (Mg+Fe²⁺)=0.32–0.56, Cr/(Cr+Al)=0.50–0.78, 2.52–8.58 wt% TiO₂], and clinopyroxene [Mg/(Mg+Fe)=0.79–0.88, Wo_44.1-45.3, En_43.9-48.0, Fs_6.8-11.0] which appeared on the liquidus together with olivine≈Fo₈₆. Redox conditions evolved from intermediate between the QFM and WM buffers to late-stage conditions of NNO+1 to NNO+2. The primary magmas crystallized in the presence of an essentially pure CO₂ fluid. The primary magmas originated at pressures >30 kbar and temperatures of 1500–1600° C, assuming equilibrium with mantle peridotite. This implies melting of the mantle source at a depth of ≈100 km within the garnet stability field followed by migration of melts into magma reservoirs located at the boundary between the upper mantle and lower crust. The temperatures and pressures of primary magma generation suggest that the Canarian plume originated in the lower mantle at depth ≈900 km that supports the plume concept of origin of the Canary Islands. Received: 23 October 1995/Accepted: 21 February 1996     

Behaviour of a small sedimentary volcanic aquifer receiving irrigation return flows: La Aldea,Gran Canaria,Canary Islands (Spain)

In many arid and semi-arid areas, intensive cultivation is practiced despite water commonly being a limiting factor. Often, irrigation water is from local aquifers or imported from out-of-area aquifers and surface reservoirs. Irrigation return flows become a significant local recharge source, but they may deteriorate aquifer water quality. La Aldea valley, located in the western sector of Gran Canaria Island (Atlantic Ocean), is a coastal, half-closed depression in altered, low-permeability volcanics with alluvium in the gullies and scree deposits over a large part of the area. This area is intensively cultivated. Irrigation water comes from reservoirs upstream and is supplemented (average 30 %) by local groundwater; supplementation goes up to 70 % in dry years, in which groundwater reserves are used up to exhaustion if the dry period persists. Thus, La Aldea aquifer is key to the water-supply system, whose recharge is mostly from return irrigation flows and the scarce local rainfall recharge on the scree formations, conveyed to the gully deposits. To quantify the hydrogeological conceptual model and check data coherence, a simplified numerical model has been constructed, which can be used as a tool to help in water management.     

Reactions between mantle xenoliths and host magma beneath La Palma (Canary Islands): constraints on magma ascent rates and crustal reservoirs

Spinel-bearing peridotitic mantle xenoliths from the 1949 eruption on La Palma were modified mineralogically and chemically during prolonged reaction with their host magma. The magmatism that brought the peridotites to the surface caused two distinct generations of xenolith fractures: (1) Old fractures are characterized by crystalline selvages with cumulus textures towards the host magma, or by polymineralic veins. They are accompanied by 0.9–2 mm wide diffusion zones where peridotite olivine became less forsteritic through diffusive exchange with the host magma. Old fractures represent most of each xenolith's surface. (2) Young fractures show no selvages and only narrow diffusion zones of <0.02 mm width. Calculations based on a model of Fe-Mg interdiffusion give an age of 6 to 83 years and <4 days for old and young fractures, respectively. A combination of these data with fluid inclusion barometry indicates that selvages and veins formed during xenolith transport rather than representing wall-rock reactions or mantle metasomatism. The results provide ample evidence for prolonged storage of the xenoliths in the crust, constraining a multi-stage magma ascent: Years to decades prior to eruption, ascending magma ruptured peridotitic wall-rock possibly through hydraulic fracturing and stoping around magma reservoirs. Magma batches transported the peridotite xenoliths to the crust at ascent rates exceeding 0.2 ms⁻¹. The xenoliths and their host magma stagnated during at least 6 years in possibly sill-like reservoirs at 7–11 km depth. The xenoliths became deposited and subsequently embedded in a mush of settled phenocrysts, while selvages and veins crystallized until the eruption commenced. At the end of the eruption, the xenoliths were finally transported to the surface within hours to days. Decompression during the rapid ascent induced internal stresses and caused renewed fragmentation of the xenoliths, producing the young fractures. Received: 25 August 1997 / Accepted: 25 November 1997     

Chemical composition of crustal xenoliths from southwestern Syria: Characterization of the upper part of the lower crust beneath the Arabian plate

The chemical bulk rock composition of 37 xenoliths, brought from depths of 25–30 km to the surface by penetrating Cenozoic alkali basaltic magma, from the Shamah Harrat, southwestern Syria, was determined by XRF spectroscopy. The geochemical character of these xenoliths points to original marls and within-plate igneous rocks. To obtain the mean chemical composition of the corresponding upper portion of the lower crust, the compositions of the 37 xenoliths were averaged and a leucogranitic and upper crustal component was added to account for assimilation by the Cenozoic magmas. This mean is more basic (SiO₂—50.5 wt%) and richer in HFSE, LREE, and LILE compared to compositions of the lower crust given by Taylor and McLennan [1985. The Continental Crust: Its Composition and Evolution. Blackwell, Oxford, 312pp.] and Rudnick and Gao [2005. Composition of the continental crust. In: Rudnick, R.L. (Ed.), The Crust. Treatise on Geochemistry, vol. 3. Elsevier, Amsterdam, pp. 1–64]. Calculations of the seismic compressional-wave velocity from our compositional mean, using the PERPLE_X computer software, yielded values around 6.85 km/s, which are in accordance with reported seismic studies for the corresponding depth levels (6.7–7.1 km/s).     

Melt generation beneath ocean islands: a U-Th-Ra isotope study from Lanzarote in the Canary Islands

New major and trace element data, and Sr, Nd, Pb, U, Th and Ra isotopes are presented for prehistoric and historic lavas from Lanzarote in the Canary Islands. These rocks are amongst the most primitive found on intraplate ocean islands ranging in composition from basanite to alkali basalt, with MgO contents >9.3% and Mg numbers >67. The youngest are from two of the three 1824 vents, the largest group of samples is from the best known eruption episode, the 1730–36 Timanfaya eruptions, a smaller group of samples are from the northeast Corona region (∼50 ky) and the oldest samples are from the Famara complex and basement massif. The rocks have some of the characteristics of HIMU OIB, including high Ce/Pb, Nb/Ce and low Nb/U and restricted ⁸⁷Sr/⁸⁶Sr (0.70209–0.70332). There is significant ²³⁰Th/²³⁸U disequilibrium (²³⁰Th excesses range from 6–76%) with some of the intermediate silica composition Corona samples showing the greatest disequilibrium. The historic samples exhibit ²²⁶Ra excess. The major and trace element data have undergone fractionation corrections to Mg numbers of 70, requiring <5% olivine fractionation, and these inferred primary compositions are used to evaluate a number of melt generation and mixing models.The fractionation-corrected compositions for the 1824 and the 1730–36 have been modelled as 1–4% melts of a source similar to primitive mantle. However, Yb is incompatible, and so the amounts of residual garnet were < ∼5%, suggesting that there was no significant contribution from garnet pyroxenite source rocks. Rather the REE and the FeO contents are both consistent with melting in the garnet-spinel transition, at depths of 60–70 km. (²³⁰Th/²³⁸U) increases slightly with increasing La/Yb in the younger rocks, and they require some form of dynamic melting model. In the preferred model the upwelling rate is kept constant, and the differences in the degrees of melting are attributed to different lengths of the melt column, with the smaller degree melts being extracted from greater depths. Strikingly, (²²⁶Ra/²³⁰Th) increases with increasing degrees of melting, and so it reflects the time since extraction from the melt column rather than variations in the melting processes. Intra-suite minor and trace element variations are due to magma mixing, and not to progressive changes in the degrees of partial melting, and it is envisaged that such magma mixing occurred during the dynamic melting processes. Dynamic melting at depths of 60–70 km suggests that the regional uplift around the Canary Islands is at least in part due to thermal erosion of the underlying lithosphere.Variations of average Ce/Yb, Tb/Yb, (²³⁰Th/²³⁸U), SiO₂ and lithospheric age for different OIB highlight how the smaller degree melts tend to be generated at greater depths, and the mean pressure of melting increases with the thickness of the lithospheric lid. However, there is no general link between (²³⁰Th/²³⁸U) and the lithospheric age or thickness, and hence the integrated degrees of melting. High buoyancy fluxes result in higher degrees of melting and low (²³⁰Th/²³⁸U) (Chabaux and Allegre, 1994), but for OIB generated within low buoyancy plumes, (²³⁰Th/²³⁸U) and the degrees of melting primarily depend on the depths of melt extraction. Differences in the average composition of low buoyancy OIB depend on the thickness of the overlying lithosphere Ellam 1992, Haase 1996, and the differences within an OIB suite, such as between the 1730-36 and 1824 lavas on Lanzarote, depend on the depth of extraction from the melt column.     

Sr-Nd-Pb isotope data for ultramafic xenoliths from Hierro,Canary Islands: Melt infiltration processes in the upper mantle

We present here Sr, Nd, and Pb-isotopic data from harzburgite (group I) and dunite-pyroxenite (group II) suite mantle xenoliths from the island of Hierro, one of the youngest and westernmost of the Canary Islands. A progressive leaching technique has been developed and applied to the whole-rock powder samples in order to identify and remove as far as possible any recent additions (host basalt and/or sea-water). Isotopic analyses of the leached residues show significant systematic differences between these two suites. Dunite-pyroxenite suite xenoliths (olivine pyroxenites, dunites and wehrlites) exhibit a relatively small range of isotopic compositions (⁸⁷Sr/⁸⁶Sr from 0.70292 to 0.70315; ¹⁴³Nd/¹⁴⁴Nd from 0.51295 to 0.51302; ²⁰⁶Pb/²⁰⁴Pb from 19.18 to 19.40) compared to the harzburgite suite (⁸⁷Sr/⁸⁶Sr from 0.70295 to 0.70320; ¹⁴³Nd/¹⁴⁴Nd from 0.51285 to 0.51296; ²⁰⁶Pb/²⁰⁴Pb from 18.85 to 19.41). In all isotope correlation diagrams the leached dunite-pyroxenite suite xenoliths plot between the Hierro basalt field and a hypothetical depleted mantle suggesting that these xenoliths may have been strongly infiltrated by Hierro-type basalt. Progressive leaching of this suite of samples showed removal of a component with more enriched Sr (higher ⁸⁷Sr/⁸⁶Sr relative to depleted mantle) and Nd (lower ¹⁴³Nd/¹⁴⁴Nd) isotopic compositions that is probably host basalt glass. The leached harzburgite suite xenoliths extend to more enriched Sr and Nd isotopic compositions than Hierro-type basalt but always have more depleted Pb. This relationship can best be explained if this suite has been subject to infiltration by earlier magmas of the Canary Island suite (in particular, those from Gran Canaria show appropriate compositional ranges), although additional infiltration by Hierro basalt cannot be ruled out. The leaching experiments for this suite mostly show removal of a radiogenic Sr component only (? seawater) which supports the interpretation of early infiltration and subsequent recrystallisation and equilibration prior to the Hierro event. Isotopic data presented in this study show that complex interaction with percolating basaltic melts of varying composition was occurring in the upper mantle beneath Hierro prior to and during the volcanic event and was probably related to the generation of earlier Canary Island magmas.     

Oxygen isotope heterogeneity of the mantle beneath the Canary Islands: a discussion of the paper of Gurenko et al.

Gurenko et al. (Contrib Mineral Petrol 162:349–363, 2011) report laser-assisted fluorination (LF) and secondary ionization mass spectrometry (SIMS) ¹⁸O/¹⁶O datasets for olivine grains from the Canary Islands of Gran Canaria, Tenerife, La Gomera, La Palma and El Hierro. As with prior studies of oxygen isotopes in Canary Island lavas (e.g. Thirlwall et al. Chem Geol 135:233–262, 1997; Day et al. Geology 37:555–558, 2009, Geochim Cosmochim Acta 74:6565–6589, 2010), these authors find variations in δ¹⁸O_ol (~4.6–6.0 ‰) beyond that measured for mantle peridotite olivine (Mattey et al. Earth Planet Sci Lett 128:231–241, 1994) and interpret this variation to reflect contributions from pyroxenite-peridotite mantle sources. Furthermore, Gurenko et al. (Contrib Mineral Petrol 162:349–363, 2011) speculate that δ¹⁸O_ol values for La Palma olivine grains measured by LF (Day et al. Geology 37:555–558, 2009, Geochim Cosmochim Acta 74:6565–6589, 2010) may be biased to low values due to the presence of altered silicate, possibly serpentine. The range in δ¹⁸O_ol values for Canary Island lavas are of importance for constraining their origin. Gurenko et al. (Contrib Mineral Petrol 162:349–363, 2011) took a subset (39 SIMS analyses from 13 grains from a single El Hierro lava; EH4) of a more extensive dataset (321 SIMS analyses from 110 grains from 16 Canary Island lavas) to suggest that δ¹⁸O_ol is weakly correlated (R ² = 0.291) with the parameter used by Gurenko et al. (Earth Planet Sci Lett 277:514–524, 2009) to describe the estimated weight fraction of pyroxenite-derived melt (Xpx). With this relationship, end-member δ¹⁸O values for HIMU-peridotite (δ¹⁸O = 5.3 ± 0.3 ‰) and depleted pyroxenite (δ¹⁸O = 5.9 ± 0.3 ‰) were defined. Although the model proposed by Gurenko et al. (Contrib Mineral Petrol 162:349–363, 2011) implicates similar pyroxenite-peridotite mantle sources to those proposed by Day et al. (Geology 37:555–558, 2009, Geochim Cosmochim Acta 74:6565–6589, 2010) and Day and Hilton (Earth Planet Sci Lett 305:226–234, 2011), there are significant differences in the predicted δ¹⁸O values of end member components in the two models. In particular, Day et al. (Geochim Cosmochim Acta 74:6565–6589, 2010) proposed a mantle source for La Palma lavas with low-δ¹⁸O (<5 ‰), rather than higher-δ¹⁸O (c.f. the HIMU-peridotite composition of Gurenko et al. in Contrib Mineral Petrol 162:349–363, 2011). Here we question the approach of using weakly correlated variations in δ¹⁸O_ol and the Xpx parameter to define mantle source oxygen isotope compositions, and provide examples of why this approach appears flawed. We also provide reasons why the LF datasets previously published for Canary Island lavas remain robust and discuss why LF and SIMS data may provide complementary information on oxygen isotope variations in ocean island basalts (OIB), despite unresolved small-scale uncertainties associated with both techniques.     

Evidence for distinct proportions of subducted oceanic crust and lithosphere in HIMU-type mantle beneath El Hierro and La Palma, Canary Islands

Shield-stage high-MgO alkalic lavas from La Palma and El Hierro (Canary Islands) have been characterized for their O-Sr-Nd-Os-Pb isotope compositions and major-, trace-, and highly siderophile-element (HSE: Os, Ir, Ru, Pt, Pd, Re) abundances. New data are also reported for associated evolved rocks, and entrained xenoliths. Clear differences in Pd/Ir and isotopic ratios for high Os (>50 ppt) lavas from El Hierro (δ¹⁸O_olivine = 5.17 ± 0.08‰; ⁸⁷Sr/⁸⁶Sr = 0.7029 to 0.7031; ε_Nd = +5.7 to +7.1; ¹⁸⁷Os/¹⁸⁸Os = 0.1481 to 0.1750; ²⁰⁶Pb/²⁰⁴Pb = 19.1 to 19.7; Pd/Ir = 6 ± 3) versus those from La Palma (δ¹⁸O_olivine = 4.87 ± 0.18‰; ⁸⁷Sr/⁸⁶Sr = 0.7031 to 0.7032; ε_Nd = +5.0 to +6.4; ¹⁸⁷Os/¹⁸⁸Os = 0.1421 to 0.1460; ²⁰⁶Pb/²⁰⁴Pb = 19.5 to 20.2; Pd/Ir = 11 ± 4) are revealed from the dataset.Crustal or lithospheric assimilation during magma transport cannot explain variations in isotopic ratios or element abundances of the lavas. Shallow-level crystal-liquid fractionation of olivine, clinopyroxene and associated early-crystallizing minerals (e.g., spinel and HSE-rich phases) controlled compatible element and HSE abundances; there is also evidence for sub-aerial degassing of rhenium. High-MgO lavas are enriched in light rare earth elements, Nb, Ta, U, Th, and depleted in K and Pb, relative to primitive mantle abundance estimates, typical of HIMU-type oceanic island basalts. Trace element abundances and ratios are consistent with low degrees (2-6%) of partial melting of an enriched mantle source, commencing in the garnet stability field (?110 km). Western Canary Island lavas were sulphur undersaturated with estimated parental melt HSE abundances (in ppb) of 0.07 ± 0.05 Os, 0.17 ± 0.16 Ir, 0.34 ± 0.32 Ru, 2.6 ± 2.5 Pt, 1.4 ± 1.2 Pd, 0.39 ± 0.30 Re. These estimates indicate that Canary Island alkali basalts have lower Os, Ir and Ru, but similar Pt, Pd and Re contents to Hawai’ian tholeiites.The HIMU affinities of the lavas, in conjunction with the low δ¹⁸O_olivine and high ²⁰⁶Pb/²⁰⁴Pb for La Palma, and elevated ¹⁸⁷Os/¹⁸⁸Os for El Hierro implies melting of different proportions of recycled oceanic crust and lithosphere. Our preferred model to explain isotopic differences between the islands is generation from peridotitic mantle metasomatised by <10% pyroxenite/eclogite made from variable portions of similar aged recycled oceanic crust and lithosphere. The correspondence of radiogenic ²⁰⁶Pb/²⁰⁴Pb, ¹⁸⁷Os/¹⁸⁸Os, elevated Re/Os and Pt/Os, and low-δ¹⁸O in western Canary Island lavas provides powerful support for recycled oceanic crust and lithosphere to generate the spectrum of HIMU-type ocean island basalt signatures. Persistence of geochemical heterogeneities throughout the stratigraphies of El Hierro and La Palma demonstrate long-term preservation of these recycled components in their mantle sources over relatively short-length scales (∼50 km).     

Lower crustal xenoliths from Mongolia and their bearing on the nature of the deep crust beneath central Asia

Rare lower crustal xenoliths found in Cenozoic alkali basalts from the Tariat region in central Mongolia and the Dariganga Plateau in south-eastern Mongolia are the only direct samples of lower crustal material known so far from central and eastern Asia. They are two-pyroxene granulites, including some garnet granulites, as well as scarce amphibolite-facies rocks. The xenoliths are broadly basaltic to andesitic in bulk chemical composition. Their igneous protoliths appear to represent underplated fractionated liquids and cumulates from such liquids. The xenoliths yield equilibration temperatures of 840 ± 30 °C (Wells, 1977) and, for Tariat garnet granulites only, pressures of 14 ± 1.5 kbar. For central Mongolia, these estimates indicate unusually great depths of origin which, however, are in line with some geophysical models for that area.

Extensive to complete kelyphitisation has affected the garnets where originally present in the Tariat suite; nevertheless, the kelyphite has largerly preserved the major element and REE compositions of the original garnet. Mineral and whole-rock Sm-Nd data obtained for three samples from Tariat and Dariganga indicate, within large errors, low or zero ages. These may either indicate that the rocks are young (Cenozoic) or that ambient temperatures in the lower crust were high enough to permit continuous isotopic equilibration on a mineral-to-mineral scale.     

Experimental melting of crustal xenoliths from Kilbourne Hole,New Mexico and implications for the contamination and genesis of magmas

Experiments (P=6.9 kb; T=900–1000°C) on four crustal xenoliths from Kilbourne Hole demonstrate the varying melting behavior of relatively dry crustal lithologies in the region. Granodioritic gneisses (samples KH-8 and KH-11) yield little melt (<5–25%) by 925°C, but undergo extensive (30–50%) melting between 950 and 1000°C. A dioritic charnockite (KH-9) begins to melt, with the consumption of all modal K-feldspar, by 900°C. It is as fertile a melt source as the granodiorites at lower temperatures, but is outstripped in melt production by the granodiorite gneisses at high temperature, yielding only 26% melt by 1000°C. A pelitic granulite (KH-12) proved to be refractory (confirming earlier predictions based on geochemistry) and did not yield significant melt even at 1000°C. All melts have the composition of metaluminous to slightly peraluminous granites and are unlikely to be individually recognizable as magma contaminants on the basis of major element chemistry. However, the relative stability of K-feldspar during partial melting will produce recognizable signatures in Ba, Eu, K/Ba, and Ba/Rb. Melts of KH-11, which retains substantial K-feldspar throughout the melting interval, are generally low in Ba (<500–800 ppm), have high K/Ba and low Ba/Rb (est.) (62–124 and 1–3, respectively). Melts of KH-9, in which all K-feldspar disappears with the onset of melting, are Ba-rich [2000–2600 ppm, K/Ba=16–22; Ba/Rb (est.) =25–47]. Melts of KH-8 have variable Ba contents; <500 ppm Ba at low temperature but >900 ppm Ba in high-temperature melts coexisting with a K-feldspar-free restite. Although REE were not measured in either feldspar or melt, the high Kspar/melt Kds for Eu suggests that the melts coexisting with K-feldspar will have strong negative Eu anomalies. Isotopic and trace element models for magma contamination need to take into account the melting behavior of isotopic reservoirs. For example, the most radiogenic (and incompatible element-rich) sample examined here (the pelitic granulite,⁸⁷Sr/⁸⁶Sr=0.757) is refractory, while samples with far less radiogenic Sr (⁸⁷Sr/⁸⁶Sr=0.708-0.732) produced substantial melt. This suggests that, in this area, the isotopic signature of contamination may be more subtle than expected. The experimental results can be used to model the petrogenesis of Oligocene volcanic rocks exposed 150 km to the NW of Kilbourne Hole, in the Black Range in the Mogollon-Datil volcanic field. The experimental results suggest that a crustal melting origin for the Kneeling Nun and Caballo Blanco Tuffs is unlikely, even though such an interpretation is permitted by Sr isotopes. Curstal contamination of a mantle-derived magma best explains the chemical and isotopic characteristics of these tuffs. Both experimental and geochemical data suggest that the rhyolites of Moccasin John Canyon and Diamond Creek could represent direct melts of granodiorite basement similar, but not identical, to the Kilbourne Hole granodiorites, perhaps slightly modified by crystal fractionation. The absence of volcanic rocks having⁸⁷Sr/⁸⁶Sr>0.74 in the region is consistent with the refractory character of the pelitic granulite.     

Melting of crustal xenoliths within ascending basalt: Example from the Kula volcanic field,western Anatolia,Turkey

During its storage or ascent, basaltic magma inevitably interacts with the surrounding rocks. In this study, schist xenoliths incorporated within ascending basalt are examined. Heating of the xenoliths combined with decompression effect of rapid magma uprise led to dehydration melting of hydrous minerals producing hercynitic spinel, melt, sillimanite and FeTi oxides. The melt is rhyolitic, strongly peraluminous (1.77 < A/CNK < 2.35) and corundum normative. It may contain up to 8 wt%FeO_t. It occurs between the foliation planes and in the intragranular environment. Dehydration melting of micas in the schist is probably related to combined effects of heating by basaltic magma and decompression due to the rapid rise. Melting of xenoliths was a progressive process at low pressure. To cite this article: H. Bayhan et al., C. R. Geoscience 338 (2006).     

Oxygen and hydrogen isotope study of high-pressure metagabbros and metabasalts (Cyclades, Greece): implications for the subduction of oceanic crust

Oxygen and hydrogen stable isotope ratios of eclogite-facies metagabbros and metabasalts from the Cycladic archipelago (Greece) document the scale and timing of fluid–rock interaction in subducted oceanic crust. Close similarities are found between the isotopic compositions of the high-pressure rocks and their ocean-floor equivalents. High-pressure minerals in metagabbros have low δ¹⁸O values: garnet 2.6 to 5.9‰, glaucophane 4.3 to 7.1‰; omphacite 3.5 to 6.2‰. Precursor actinolite that was formed during the hydrothermal alteration of the oceanic crust by seawater analyses at 3.7 to 6.3‰. These compositions are in the range of the δ¹⁸O values of unaltered igneous oceanic crust and high-temperature hydrothermally altered oceanic crust. In contrast, high-pressure metabasalts are characterised by ¹⁸O-enriched isotopic compositions (garnet 9.2 to 11.5‰, glaucophane 10.6 to 12.5‰, omphacite 10.2 to 12.8‰), which are consistent with the precursor basalts having undergone low-temperature alteration by seawater. D/H ratios of glaucophane and actinolite are also consistent with alteration by seawater. Remarkably constant oxygen isotope fractionations, compatible with isotopic equilibrium, are observed among high-pressure minerals, with Δ_{glaucophane−garnet} = 1.37 ± 0.24‰ and Δ_{omphacite−garnet} = 0.72 ± 0.24‰. For the estimated metamorphic temperature of 500 °C, these fractionations yield coefficients in the equation Δ = A * 10⁶/T ² (in Kelvin) of A_{glaucophane−garnet} = 0.87 ± 0.15 and A_{omphacite−garnet} = 0.72 ± 0.24. A fractionation of Δ_{glaucophane–actinolite} = 0.94 ± 0.21‰ is measured in metagabbros, and indicates that isotopic equilibrium was established during the metamorphic reaction in which glaucophane formed at the expense of actinolite. The preservation of the isotopic compositions of gabbroic and basaltic oceanic crust and the equilibrium fractionations among minerals shows that high-pressure metamorphism occurred at low water/rock ratios. The isotopic equilibrium is only observed at hand-specimen scale, at an outcrop scale isotopic compositional differences occur among adjacent rocks. This heterogeneity reflects metre-scale compositional variations that developed during hydrothermal alteration by seawater and were subsequently inherited by the high-pressure metamorphic rocks. Received: 4 January 1999 / Accepted: 7 July 1999     

Lower crustal granulite xenoliths from the Pannonian Basin,Hungary, Part 2: Sr–Nd–Pb–Hf and O isotope evidence for formation of continental lower crust by tectonic emplacement of oceanic crust

Mafic granulite xenoliths from the lower crust of the Pannonian Basin are dominated by LREE-depleted bulk-rock compositions. Many of these have MORB-like ¹⁴³Nd/¹⁴⁴Nd but ⁸⁷Sr/⁸⁶Sr is elevated relative to most MORBs. Their '¹⁸O values cover a wide range from +3.8 to +9.5‰. A group of LREE-enriched mafic granulites have higher ⁸⁷Sr/⁸⁶Sr (0.704-0.708) and lower ¹⁴³Nd/¹⁴⁴Nd (0.5128-0.5124), with higher '¹⁸O values on average (+7.8 to +10.6‰) than the LREE-depleted granulites. The LREE-enriched granulites are, however, isotopically similar to newly discovered metasedimentary granulite xenoliths. A sublinear correlation in )Hf-)Nd isotope space has a shallower slope than the crust-mantle array, with the metasedimentary rocks forming the low )Hf end member; the radiogenic end is restricted to the LREE-depleted granulites and these overlap the field of MORB. Pb isotopes for the LREE-depleted samples are less radiogenic on average than those of the LREE-enriched and metasedimentary xenoliths, and metasedimentary granulites have consistently higher ²⁰⁸Pb/²⁰⁴Pb. The wide range in '¹⁸O over a restricted range in Nd and Sr isotope values, in combination with the predominance of LREE-depleted trace-element compositions, is consistent with an origin as a package of hydrothermally altered oceanic crust. The existence of '¹⁸O values lower than average MORB and/or mantle peridotite requires that at least some of these rocks were hydrothermally altered at high temperature, presumably in the oceanic lower crust. The low ¹⁴³Nd/¹⁴⁴Nd of the LREE-enriched mafic granulites cannot be explained by simple mixing between a LREE-depleted melt and an enriched component, represented by the recovered metasediments. Instead, we interpret these rocks as the metamorphic equivalent of the shallowest levels of the ocean crust where pillow basalts are intimately intercalated with oceanic sediments. A possible model is accretion of oceanic crustal slices during subduction and convergence, followed by high-grade metamorphism during the Alpine orogeny.     

Carbonate tufas as archives of climate and sedimentary dynamic in volcanic settings,examples from Gran Canaria (Spain)

Three Holocene tufas from Gran Canaria volcanic island were studied with the aim of deciphering their sedimentary evolution through space and time. Las Temisas tufa (south-eastern arid part of the island) is dominantly composed of oncoids, intraclasts, phytoclasts, coated stems, minor thin stromatolites, and a high amount of siliciclastics. It was deposited in a fluvial system with variable flow velocities and palustrine conditions areas, which alternated with high energy events. Azuaje tufa (northern humid part of the island) is composed of coated stems, stromatolites, oncoids and phytoclasts, with relatively low amounts of siliciclastics, suggesting slow-flowing and palustrine conditions and a relatively low incidence of (high energy) floodings. Los Berrazales tufa (north-west of Gran Ganaria, the most humid one), is mainly composed of coated stems and crystalline crusts, formed in a laminar flow regime. Dominant clastic sedimentation in Las Temisas and high calcite growth rates in Los Berrazales led to a poor development of stromatolites in comparison with Azuaje. Las Temisas and Azuaje deposits have similar upward evolution with decreasing trend in siliciclastics and increasing trend in carbonates. However, Las Temisas has higher siliciclastic and lower phytoclastic contents suggesting a less vegetated area and more arid climate than in the other deposits. Additionally, tufas record local events common in volcanic terrains. Azuaje presents three units bounded by erosive discontinuities, which reveal significant erosion by enhanced runoff that could be caused by loss of vegetation due to wildfires related to volcanic eruptions at headwaters. Las Temisas record a possible interruption in sedimentation represented by aligned boulders due to rockfalls from the hillsides. These deposits formed from waters with similar chemistry providing to the carbonates their similar signals in δ¹³C–δ¹⁸O stable isotopes and ⁸⁷Sr/⁸⁶Sr ratios like that of the volcanic rocks. This work shows how, in volcanic areas, tufas are unique archives of the climate, vegetation and volcanic-related processes, because all imprint the sedimentary regime of tufa deposition.     

Glass-bearing crustal xenoliths (buchites) erupted during the recent activity of Stromboli (Aeolian Islands)

Three xenoliths erupted as ejecta during recent violent explosion of Stromboli volcano (Aeolian Islands) were investigated in this paper. They consist of high-temperature mineral association (cordierite, hercynite spinels, sillimanite, ±plagioclase, ±mullite, ±corundum) and abundant glass (10–70 vol.%), and may be classified as buchites. The peraluminous composition of the xenoliths, their trace element distribution and REE patterns support their origin from granulite- and amphibolite-facies metapelites of the Calabrian continental crust, which is considered the crystalline basement beneath Stromboli. Buchites have an isotopic composition comparable to that of Stromboli extrusives and significantly different from that of the Calabrian basement.

The glass is generally colourless and has a Si–Al–alkali-rich composition, except for one sample where a Fe–Mg–Ca-rich reddish-brown glass also occurs. These two kinds of glass show complicated textures where patches of reddish-brown glass are often surrounded by plagioclase and/or cordierite or forms streaks and swirls with the colourless glass. Cordierite, plagioclase and oxides have different compositions according to their position in the xenoliths. Ca-rich plagioclase (An_72–95), Mg-poor cordierite (Mg-values 47–66) and Al-rich spinels are in the inner portions of the xenoliths and associated with colourless glass; on the contrary, close to the contact with the host lava or associated with coloured glass, cordierite shows higher Mg-values, Ti–Fe-bearing oxides occur and plagioclase is chemically similar to the basalt phenocrysts (An_66–71).

The abundant and fresh glass and the idiomorphic shape of the high-temperature minerals suggest that the xenoliths were hold in the basaltic magma, before its extrusion, for a significant time to allow their partial or nearly complete melting and subsequent nucleation and growth of new phases. During this stage, the interaction between the anatectic liquid and the basaltic magma affected the original isotopic composition of the xenoliths and, in some cases, produced glass and mineral phases (cordierite, plagioclase and oxides) with different composition.     

The Petrology of the Tholeiites through Melilite Nephelinites on Gran Canaria, Canary Islands: Crystal Fractionation, Accumulation, and Depths of Melting

We report major and trace element X-ray fluorescence (XRF) datafor mafic volcanics covering the 15-Ma evolution of Gran Canaria,Canary Islands. The Miocene (12–15 Ma) and Pliocene-Quaternary(0–6 Ma) mafic volcanics on Gran Canaria include picrites,tholeiites, alkali basalts, basanites, nephelinites, and melilitenephelinites. Olivineclinopyroxene are the major fractionatingor accumulating phases in the basalts. Plagioclase, Fe–Tioxide, and apatite fractionation or accumulation may play aminor role in the derivation of the most evolved mafic volcanics.The crystallization of clinopyroxene after olivine and the absenceof phenocrystic plagioclase in the Miocene tholeiites and inthe Pliocene and Quaternary alkali basalts and basanites withMgO>6 suggests that fractionation occurred at moderate pressure,probably within the upper mantle. The presence of plagioclasephenocrysts and chemical evidence for plagioclase fractionationin the Miocene basalts with MgO<6 and in the Pliocene tholeiitesis consistent with cooling and fractionation at shallow depth,probably during storage in lower-crustal reservoirs. Magma generationat pressures in excess of 3•0–3•5 GPa is suggestedby (a) the inferred presence of residual garnet and phlogopiteand (b) comparison of FeO¹ cation mole percentages and the CIPWnormative compositions of the mafic volcanics with results fromhigh-pressure melting experiments. The Gran Canaria mafic magmaswere probably formed by decompression melting in an upwellingcolumn of asthenospheric material, which encountered a mechanicalboundary layer at {small tilde}100-km depth.     

Lower crustal xenoliths from Junan,Shandong province and their bearing on the nature of the lower crust beneath the North China Craton

Geochronological, petrological and geochemical studies were performed on the granulite xenoliths from a Late Cretaceous basaltic breccia dike in Junan, Shandong province, eastern China. These xenoliths show close similarities to the Nushan granulite xenoliths from the southern margin of the North China Craton (NCC) and the Archean granulite terrains in terms of mineralogy and bulk rock compositions, but are quite different from the Hanuoba mafic granulite xenoliths from the northern NCC. In-situ zircon U–Pb age and Hf isotopic analyses, together with geochemical data reveal that the protolith of these xenoliths was formed around 2.3 Ga ago, through assimilation–fractional crystallization of a mafic magma. P–T conditions of these xenoliths suggest that the lower crust beneath the Junan region reaches to a depth of 35 km, which agree well with the result deduced from various geophysical methods. The consistent petrological and seismic Moho depths, the observed velocity structure and calculated velocity of these xenoliths imply the absence of underplating induced crust–mantle transition zone, which was well formed in the northern NCC. Compared to 40–50 km depth of the lower crust in Early Jurassic, the lower crust beneath Junan extended to a depth of 30 km in Late Cretaceous, suggesting that the lower crust of NCC was significantly thinned during Late Mesozoic.