Petrogenesis of late stage magmatism at Hold with Hope, East Greenland

The Myggbukta caldera complex and a swarm of basic dykes constitute the latest Tertiary magmatism in the Hold with Hope region, East Greenland. The Sr and Nd isotope ratios of these rocks show coherent variations which extend to high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd values and require a contribution from continental lithosphere. Broad correlations with major element differentiation indices suggest that the continental component was incorporated during magmatic differentiation thereby favouring a crustal contamination process. Trace element concentrations are strongly correlated with isotopic compositions but display ranges for many incompatible elements which extend beyond likely crustal contaminant compositions. This is readily modelled by AFC processes in which the dominant cause of trace element enrichment is the concentration effect of fractional crystallisation rather than the composition of the contaminant. The simplest such models still require unrealistically high degrees of fractional crystallisation to explain the ten-fold enrichment of some trace elements. This can be overcome if the primary magmas entering the crust already had highly variable trace element compositions. Such variability is readily achieved if melts from different parts of the melting column escape without thorough homogenization. An AFC model which incorporates variability in parental magma composition is then able to simulate the range of compositions observed at Hold with Hope. This carries the implication that the variations observed are more readily attributed to changes in uncontaminated parental magma than to variations in the composition or amount of contaminant. Received: 5 March 1998 / Accepted: 16 June 1998     

Crustal assimilation during turbulent magma ascent (ATA); new isotopic evidence from the Mull Tertiary lava succession,N. W. Scotland

Assimilation of crustal rocks with concomitant fractional crystallisation (AFC) is a well documented phenomenon in many igneous suites, but geochemical evidence from the Tertiary Mull lava succession suggests that in these magmas crustal contamination occurred by a distinctly different mechanism. Lavas from the lower half of the Mull Plateau group (MPG) can be divided into two broad sub-types; high (>8%) MgO basalts with elevated Ba and K; and lower MgO (<8%) basaltic-hawaiites with lower Ba and K. The lower crust and most of the upper crust beneath Mull is probably of Lewisian age. The Sr-, Nd-and Pb-isotope compositions of local Lewisian crustal samples yield the following ranges: ⁸⁷Sr/⁸⁶Sr=0.71002–0.72348, ¹⁴³Nd/¹⁴⁴Nd=0.51045–0.51058 and ²⁰⁶Pb/²⁰⁴Pb=14.0–14.6. Ten lavas have also been analysed and yield the following ranges: ⁸⁷Sr/⁸⁶Sr=0.7028–0.7042, ¹⁴³Nd/¹⁴⁴Nd=0.51214–0.51230 and ²⁰⁶Pb/²⁰⁴Pb=15.1–17.9. However, within this range, it is predominantly the more primitive mafic compositions, with elevated Mg, Ba and K, that show the lowest Nd- and Pb-, and the highest Sr-isotope values. Modelling of these isotopic results, in conjunction with major and trace element data, show that: (1) contamination by Lewisian lower crustal material does occur; (2) that the process involved was not one of assimilation with concomitant fractional crystallisation (AFC). The proposed contamination process is one whereby the hottest (most MgO rich) magmas have assimilated acidic partial melts of Lewisian lower crust during turbulent ascent (ATA) through thin, poorly connected dyke- and sill-like magma chambers. The chemical composition of the contaminated lavas can be modelled successfully through addition of 5% acidic Lewisian crust to an uncontaminated lava. In contrast, the more evolved magmas — which probably fractionated at sub-crustal levels — were either not hot enough to molt significant amounts of crust, or did not ascend turbulently because of their higher viscosity, and so are less contaminated with crust.     

Petrogenesis of rhyolites and trachytes from the Deccan Trap: Sr,Nd and Pb isotope and trace element evidence

Trachytes and rhyolites from Salsette Island, north of Bombay, have distinctive trace element and isotope features which mark them out from typical crustal melts. Their highly incompatible trace element and Sr-, Nd and Pb isotope ratios are similar to those of the associated Deccan flood basalts. Thus the rhyolites and trachytes are closely related to the basalts, and a striking compositional gap between 50 and 65% SiO₂ suggests that the high SiO₂ rocks evolved by 10–15% partial melting followed by variable amounts of fractional crystallisation. The source material could have been basalt within the Deccan Trap, or related gabbroic rocks in deep crustal sill complexes. The rhyolites yield an Rb-Sr whole rock age of 61.5±1.9 Ma, with a slightly high initial ⁸⁷Sr/⁸⁶Sr=0.7085±18. It is argued that crustal extension provides a suitable regime for the generation of acid magmas by partial melting of associated basic rocks.     

A quantitative approach to trace element and Sr isotope evolution in the Adamello batholith (northern Italy)

A development of De Paolo's mathematical procedure (1981) for magmatic AFC (Assimilation-Fractional Crystallization) processes is discussed with respect to both trace element and Sr isotopic ratio behaviours during the genesis and evolution of Adamello batholith (northern Italy). Resolution of a two equation-system (one relative to ⁸⁷Sr/⁸⁶Sr ratio variation in a magma generated by an AFC process, the other to its trace element content variations) gives the F (mass of magma at time t/mass of initial magma) and D (bulk partition coefficient) values, by which one can deduce the r (rate of assimilation/rate of crystallization) value during each step of magmatic evolution. This quantitative approach suggests that: 1) there was a common precursor magma for all the Adamello granitoids, with a Mg-rich tholeiitic composition; 2) each intrusive unit appears to have been generated by different extents of AFC; 3) the trace element distribution in the magma seems essentially influenced by mineral fractionation, rather than by the composition of the assimilated crustal material.     

Geochemistry of the Adamello massif (northern Italy)

The Tertiary Adamello massif, outcropping over an area of more than 550 km² in the southern Alps (northern Italy) is composed mainly of granitoid rocks (granodiorite, tonalite, quartz diorite) with minor amounts of diorite and gabbro. The major and trace element composition of these rocks is comparable to calc-alkaline volcanic rocks of continental margins. The granitoid rocks display spatial and temporal variations in their composition, particularly in Na, P, Sr, La, Nb and Y contents and ⁸⁷Sr/⁸⁶Sr ratios. The variations were probably produced by concurrent contamination/wall-rock assimilation and fractional crystallization of high-alumina basaltic magma.     

Enriched mantle – Dupal signature in the genesis of the Jurassic Ferrar tholeiites from Prince Albert Mountains (Victoria Land, Antarctica)

The major, trace (including rare earth) element abundances, and Sr-Nd-Pb isotopic compositions, have been analysed for andesitic basalt and andesitic sills and lavas of the Jurassic Ferrar Magmatic Province, Prince Albert Mountains, Antarctica. The typical “crustal signature” of the Ferrar magmatism, characterized by relatively high SiO₂, LREE and LILE contents in these samples, is associated with high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd. Systematic correlations of major and trace elements indicate that fractional crystallization was important. However, increases in incompatible elements are positively correlated with initial ⁸⁷Sr/⁸⁶Sr, suggestive of crustal assimilation processes. The observed correlations between initial ⁸⁷Sr/⁸⁶Sr and LREE enrichments have been modelled by an AFC process, starting from the least evolved sample and assuming the compositions of the orthogranulites of Victoria Land as contaminants. The REE patterns of the least evolved Ferrar rocks approach those of E-type MORB, differing only by higher LREE/IREE. The enrichment in LREE, accompanying high initial ⁸⁷Sr/⁸⁶Sr, ²⁰⁷Pb/²⁰⁴Pb and low ¹⁴³Nd/¹⁴⁴Nd compared with E-type MORB, can be explained by interaction of “primary Ferrar basalt” with crystalline basement. We propose a petrological model whereby Ferrar magmas were generated through high degrees of melting of an E-type MORB mantle source, and subsequently these “primary” melts underwent AFC processes inheriting a crustal signature. The Sr-Nd-Pb isotopic compositions required by the AFC model for the primary Ferrar basalt are similar to those of the Dupal signature of the oceanic basalts of the Southern Hemisphere (Hart 1984). Transantarctic Mountains would have been located inside the Dupal anomaly in pre-Gondwana dispersion times. Received: 21 April 1998 / Accepted: 25 January 1999     

Generation of a crust-mantle magma mixture: magma sources and contamination at Cerro Panizos,central Andes

 Cerro Panizos, a large caldera in the central Andes Mountains, produced two large dacitic ignimbrites at 7.9 Ma and 6.7 Ma and many andesitic and dacitic lava flows and domes. The older rhyodacitic Cienago Ignimbrite represents the most silicic magma erupted by the system. The younger, much larger volume dacitic Cerro Panizos Ignimbrite is very crystal-rich, containing up to 50% biotite, plagioclase, and quartz crystals in the pumice. It is weakly zoned, with most of the zoning apparent between two main cooling units. Major and most trace elements show little variation through the Cerro Panizos Ignimbrite, but the small range of composition is consistent with typical fractionation trends. Sr, Nd, and Pb isotopic ratios are very “crustal”, with initial ⁸⁷Sr/⁸⁶Sr values of 0.711 to 0.715, ɛ_Nd values of –7.5 to –10.2, and nearly invariant Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb=18.85, ²⁰⁷Pb/²⁰⁴Pb=15.67, and ²⁰⁸Pb/²⁰⁴Pb=38.80). The limited zonation observed in the Cerro Panizos Ignimbrite is explained by impeded crystal settling due to high crystal content. The magma body was a crystal-liquid mush before ascent to the pre-eruption crustal levels. Crystals formed, but did not separate easily from the magma. Limited fractionation of plagioclase and biotite may have occurred, but the composition was largely controlled by lower crustal MASH processes. AFC modeling shows that the Cerro Panizos magmas resulted from a mixture of roughly equal proportions of late Miocene mantle-derived basalts and melts from ∼1.0 Ga (Grenville age) lower crust. This occurred in a MASH zone in the lower crust, and set the crustal isotopic ratios observed in the Cerro Panizos magmas. The great thickening of the crust beneath the central Andes Mountains sent upper and middle crustal rock types to lower crustal (and deeper) depths, and this explains the “upper crustal” isotopic signatures of the Cerro Panizos rocks. Minor upper crustal assimilation of early Miocene volcanic or subvolcanic rocks produced much of the isotopic variation seen in the system. The nearly invariant high Pb isotopic values and high Pb concentrations indicate that Pb came almost entirely from the crustal source, and was little altered by any subsequent upper crustal assimilation. This Pb signature is isotopically similar to that of the southern Bolivian Tin Belt, suggesting a widely distributed Pb source. The great difference between compositions of Miocene and Quaternary central Andean volcanic rocks is explained by crustal thickening in early Miocene time leading to abundant lower crustal water and associated fluxed melting during the time of the earlier eruptions. The lower crust dried out considerably by Quaternary time, so less crustal component is present. Received: 22 December 1994 / Accepted: 13 September 1995     

Crustal thermal state and origin of silicic magma in Iceland: the case of Torfajökull,Ljósufjöll and Snæfellsjökull volcanoes

Pleistocene and Holocene peralkaline rhyolites from Torfajökull (South Iceland Volcanic Zone) and Ljósufjöll central volcanoes and trachytes from Snæfellsjökull (Snæfellsnes Volcanic Zone) allow the assessment of the mechanism for silicic magma genesis as a function of geographical location and crustal geothermal gradient. The low δ¹⁸O (2.4‰) and low Sr concentration (12.2 ppm) measured in Torfajökull rhyolites are best explained by partial melting of hydrated metabasaltic crust followed by major fractionation of feldspar. In contrast, very high ⁸⁷Sr/⁸⁶Sr (0.70473) and low Ba (8.7 ppm) and Sr (1.2 ppm) concentrations measured in Ljósufjöll silicic lavas are best explained by fractional crystallisation and subsequent ⁸⁷Rb decay. Snæfellsjökull trachytes are also generated by fractional crystallisation, with less than 10% crustal assimilation, as inferred from their δ¹⁸O. The fact that silicic magmas within, or close to, the rift zone are principally generated by crustal melting whereas those from off-rift zones are better explained by fractional crystallisation clearly illustrates the controlling influence of the thermal state of the crust on silicic magma genesis in Iceland.     

Transition from calc-alkaline to potassium-rich magmatism in subduction environments: geochemical and Sr, Nd, Pb isotopic constraints from the island of Vulcano (Aeolian arc)

The problem of mantle metasomatism vs. crustal contamination in the genesis of arc magmas with different potassium contents has been investigated using new trace element and Sr–Nd–Pb isotopic data on the island of Vulcano, Aeolian arc. The analysed rocks range in age from 120 ka to the present day, and cover a compositional range from basalt to rhyolite of the high-K calc-alkaline (HKCA) to shoshonitic (SHO) and potassic (KS) series. Older Vulcano products (>30 ka) consist of HKCA–SHO rocks with SiO₂=48–56%. They show lower contents of K₂O, Rb and of several other incompatible trace element abundances and ratios than younger rocks with comparable degree of evolution. ⁸⁷Sr/⁸⁶Sr ranges from 0.70417 to 0.70504 and increases with decreasing MgO and compatible element contents. ²⁰⁶Pb/²⁰⁴Pb ratios display significant variations (19.31 to 19.76) and are positively correlated with MgO, ¹⁴³Nd/¹⁴⁴Nd (0.512532–0.512768), ²⁰⁷Pb/²⁰⁴Pb (15.66–15.71) and ²⁰⁸Pb/²⁰⁴Pb (39.21–39.49). Overall, geochemical and isotopic data suggest that the evolution of the older series was dominated by assimilation–fractional crystallisation (AFC) with an important role for continuous mixing with mafic liquids. Magmas erupted within the last 30 ka consist mostly of SHO and KS intermediate and acid rocks, with minor mafic products. Except for a few acid rocks, they display moderate isotopic variations (e.g. ⁸⁷Sr/⁸⁶Sr=0.70457–0.70484; ²⁰⁶Pb/²⁰⁴Pb=19.28–19.55, but ²⁰⁷Pb/²⁰⁴Pb=15.66–15.82), which suggest an evolution by fractional crystallisation, or in some cases by mixing, with little interaction with crustal material. The higher Sr isotopic ratios (⁸⁷Sr/⁸⁶Sr=0.70494–0.70587) of a few, low-volume, intermediate to acid rocks support differentiation by AFC at shallow depths for some magma batches. New radiogenic isotope data on the Aeolian islands of Alicudi and Stromboli, as well as new data for lamproites from central Italy, are also reported in order to discuss along-arc compositional variations and to evaluate the role of mantle metasomatism. Geochemical and petrological data demonstrate that the younger K-rich mafic magmas from Vulcano cannot be related to the older HKCA and SHO ones by intra-crustal evolutionary processes and point to a derivation from different mantle sources. The data from Alicudi and Stromboli suggest that, even though interaction between magma and wall rocks of the Calabrian basement during shallow level magma evolution was an important process locally, a similar interpretation can be extended to the entire Aeolian arc. Received: 27 September 1999 / Accepted: 24 May 2000     

Petrochemistry of the south Marmara granitoids, northwest Anatolia, Turkey

Post-collision magmatic rocks are common in the southern portion of the Marmara region (Kap?da?, Karabiga, Gönen, Yenice, Çan areas) and also on the small islands (Marmara, Av?a, Pa?aliman?) in the Sea of Marmara. They are represented mainly by granitic plutons, stocks and sills within Triassic basement rocks. The granitoids have ages between Late Cretaceous and Miocene, but mainly belong to two groups: Eocene in the north and Miocene in the south. The Miocene granitoids have associated volcanic rocks; the Eocene granitoids do not display such associations. They are both granodioritic and granitic in composition, and are metaluminous, calc-alkaline, medium to high-K rocks. Their trace elements patterns are similar to both volcanic-arc and calc-alkaline post-collision intrusions, and the granitoids plot into the volcanic arc granite (VAG) and collision related granite areas (COLG) of discrimination diagrams. The have high ⁸⁷Sr/⁸⁶Sr (0.704–0.707) and low ¹⁴³Nd/¹⁴⁴Nd (0.5124–0.5128). During their evolution, the magma was affected by crustal assimilation and fractional crystallization (AFC). Nd and Sr isotopic compositions support an origin of derivation by combined continental crustal AFC from a basaltic parent magma. A slab breakoff model is consistent with the evolution of South Marmara Sea granitoids.     

The geochemistry of potassic lavas from Vulsini,central Italy and implications for mantle enrichment processes beneath the Roman region

Major and trace element and ¹⁴³Nd/¹⁴⁴Nd (0.51209–0.51216) and ⁸⁷Sr/⁸⁶Sr (0.70879–0.71105) isotope analyses are presented on a representative group of lavas from the Vulsini district of the Roman magmatic province. Three distinct series are identified; the high-K and low-K series are similar to those described from other Italian volcanoes, while the third is represented by a group of relative ly undifferentiated leucite basanites which are thought to be near-primary mantle melts. Major and trace element variations within the high-K series are consistent with fractional crystallisation from a parental magma similar to the most magnesian leucitites. Crustal contamination resulted in an increase in ⁸⁷Sr/⁸⁶Sr with increasing fractionation, but it was superimposed on magmas which had already inherited a range of incompatible element and isotope ratios from enrichment processes in the sub-continental mantle. These are reviewed using the available results from Vulsini, Roccamonfina and Ernici. Transition element abundances and Ta/Yb ratios indicate that the pre-enrichment mantle was similar to that of E-type MORB, and that these elements were not mobilised by the enrichment process. Mixing calculations suggest that three components were involved in the enrichment process; mantle comparable with the source of MORB, and two other components rich in trace elements. One, the low-K component, had high Sr/Nd, Th/Ta and Ba/Nb and no europium anomaly while the second had lower Sr/Nd, a negative europium anomaly and very high Th/Ta. It was also characterised by low Nb/Ba and high Rb/Ba ratios, similar to those reported from phlogopite-rich peridotite xenoliths. The trace element enrichment processes are therefore thought to have occurred in the mantle wedge above a subduction zone with the trace element characteristics of the high-K end-member reflecting the subduction of sediments and the stabilisation of mantle phlogopite.     

Early Cretaceous Basaltic and Rhyolitic Magmatism in Southern Uruguay Associated with the Opening of the South Atlantic

The Early Cretaceous volcanic rocks of southern Uruguay comprisemafic and felsic volcanics. The position of these outcrops atthe southern edge of the Paraná–Etendeka continentalflood basalt province provides an opportunity to investigatepossible lateral variations in both mafic and more evolved rocktypes towards the margins of such an area of plume-related magmatism.The mafic lavas are divided into two compositionally distinctmagma types. The more voluminous Treinte Y Trés magmatype is similar to the low-Ti basalts of the Paraná floodbasalt province. The Santa Lucía magma type is a distinctand rare basalt type with ocean-island basalt type asthenosphericaffinities (high Nb/La, low ⁸⁷Sr/⁸⁶Sr_i). The felsic volcanicsare divided into two series, the Lavalleja Series and the AigüaSeries. The Lavalleja Series are chemically and isotopicallysimilar to the Paraná–Etendeka low-Ti rhyolites,and are considered to be related to the Treinte Y Tréslavas by extensive fractionation and crustal assimilation. TheAigüa Series have low ¹⁴³Nd/¹⁴⁴Nd_i and low ⁸⁷Sr/⁸⁶Sr_i andunlike the rhyolites of the Paraná, are interpreted asmelts of pre-existing mafic lower crust that subsequently underwentextreme fractionation. The differences observed in the felsicsuites may be linked to differences in the volumes of the associatedbasalts and the amounts of extension. KEY WORDS: South America; flood basalts; felsic volcanics; crustal melts; plume     

Origin of calc-alkaline series lavas at Medicine Lake Volcano by fractionation,assimilation and mixing

The results of experimental studies and examination of variations in major elements, trace elements and Sr isotopes indicate that fractionation, assimilation and magma mixing combined to produce the lavas at Medicine Lake Highland. Some characteristics of the compositional differences among the members of the calc-alkalic association (basalt-andesite-dacite-rhyolite) can be produced by fractional crystallization, and a fractionation model reproduces the major element trends. Other variations are inconsistent with a fractionation origin. Elevated incompatible element abundances (K and Rb) observed in lavas intermediate between basalt and rhyolite can be produced through assimilation of a crustal component. An accompanying increase in ⁸⁷Sr/⁸⁶Sr from ∼ 0.07030 in basalt to ∼0.7040 in rhyolite is also consistent with crustal assimilation. The compatible trace element contents (Ni and Sr) of intermediate lavas can not be produced by fractional crystallization, and suggest a magma-mixing origin for some lavas. Unusual phenocryst assemblages and textural criteria in these lavas provide additional evidence for magma mixing. A phase diagram constructed from the low pressure melting experiments identifies a distributary reaction point, where olivine+augite react to pigeonite. Parental basalts reach this point at low pressures and undergo iron-enrichment at constant SiO₂ content. The resulting liquid line of descent is characteristic of the tholeiitic trend. Calc-alkalic differentiation trends circumvent the distributary reaction point by three processes: fractionation at elevated pH₂O, assimilation and magma mixing.     

Strontium isotopic and chemical variations of the granitic rocks in the Tsukuba district,Japan

Initial ⁸⁷Sr/⁸⁶Sr ratios, major and trace element compositions have been determined for the Paleogene granitic rocks in the Tsukuba district, Japan. Isotopic ages strongly suggest that the granitic rocks (seven units) were continuously emplaced and solidified during a short time interval. Initial ⁸⁷Sr/⁸⁶Sr ratios for seven granitic units vary from 0.7082 to 0.7132, while sedimentary and metasedimentary country rocks have ratios at the time of granitic magma emplacement ranging from 0.7149 to 0.7298. Continuous linear arrays for the granitic rocks in the diagrams of initial ⁸⁷Sr/⁸⁶Sr ratios versus some chemical parameters can be explained by either of following two processes. One is the assimilation — fractional crystallization (AFC) process between the parental magma (SiO₂ of 68% and initial ratio of 0.7078) and sedimentary country rocks, and the other is magma mixing process between above parental magma and sediment derived acidic magma (melt) (SiO₂ of 75%). The high initial ratios (0.7078–0.7098) for basic rocks such as gabbro or diorite in the Tsukuba district and the similar characteristics observed in the rocks of Ryoke belt (SW Japan) suggest that the parental magma had the same source region as the basic rocks, probably the lower crustal source.     

The evolution of a silicic magma system: isotopic and chemical evidence from the Woods Mountains volcanic center,eastern California

The isotopic compositions of Nd and Sr and concentrations of major and trace elements were measured in flows and tuffs of the Woods Mountains volcanic center of eastern California to assess the relative roles of mantle versus crustal magma sources and of fractional crystallization in the evolution of silicic magmatic systems. This site was chosen because the contrast in isotopic composition between Precambrian-to-Mesozoic country rocks and the underlying mantle make the isotope ratios sensitive indicators of the proportions of crustal- and mantle-derived magma. The major eruptive unit is the Wild Horse Mesa tuff (15.8 m.y. old), a compositionally zoned rhyolite ignimbrite. Trachyte pumice fragments in the ash-flow deposits provide information on intermediate composition magma types. Crustal xenoliths and younger flows of basalt and andesite (10 m.y. old) provide opportunities to confirm the isotopic compositions of potential mantle and crustal magma sources inferred from regional patterns. The trachyte and rhyolite have _Nd values of -6.2 to -7.5 and initial ⁸⁷Sr/⁸⁶Sr ratios mostly between 0.7086 and 0.7113. These magmas cannot have been melted directly from the continental basement because the _Nd values are too high. They also cannot have formed by closed system fractional crystallization of basalt because the ⁸⁷Sr/⁸⁶Sr ratios are higher than likely values for parental basalt. Both major and trace element variations indicate that crystal fractionation was an important process. These results require that the silicic magmas are end products of the evolution of mantle-derived basalt that underwent extensive fractional crystallization accompanied by assimilation of crustal rock. The mass fraction of crustal components in the trachyte and rhyolite is estimated to be between 10% and 40%, with the lower end of the range considered more likely. The generation of magmas with SiO₂ contents greater than 60% appears to be dominated by crystal fractionation with minimal assimilation of upper crustal rocks.     

The geochemical and Sr–Nd isotopic characteristics of Eocene to Miocene NW Anatolian granitoids: Implications for magma evolution in a post-collisional setting

Early Eocene to Early Miocene magmatic activity in northwestern Anatolia led to the emplacement of a number of granitoid plutons with convergent margin geochemical signatures. Granitoid plutons in the area are mainly distributed within and north of the suture zone formed after the collision of the Anatolide-Tauride platform with the Pontide belt. We present geochemical characteristics of three intrusive bodies in the region in order to identify their source characteristics and geodynamic significance. Among these, the Çataldağ and Ilıca-Şamlı plutons are located to the north and the Orhaneli pluton is located to the south of the IAESZ (Izmir-Ankara-Erzincan Suture Zone). The plutons are calc-alkaline, metaluminous, and I-type with compositions from granite to monzonite. They display clear enrichments in LILE and LREE and depletions in HFSE relative to N-MORB compositions and have high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd ratios.The results of theoretical Fractional Crystallization (FC) model show that the samples are affected by fractionation of K-feldspar, plagioclase, biotite and amphibole. Assimilation and Fractional Crystallization (AFC) modeling indicates that the r value, the proportion of variable contamination to fraction, is high, indicating significant crustal contamination in the genesis of granitoid magmas. Combined evaluation of isotopic and trace element data indicates that the granitoids are the products of mantle-derived mafic magmas variably differentiated by simultaneous crustal contamination and fractional crystallization in lower to middle crustal magma chambers in a post-collisional setting.     

The geochemistry and petrogenesis of the late-Cretaceous picrites and basalts of Curaçao,Netherlands Antilles: a remnant of an oceanic plateau

The island of Curaçao in the southern Caribbean Sea is composed mainly of a thick sequence (>5?km) of pillow lavas, grading upwards from picrites at the base of the exposed section, to basalts nearer the top. Modelling suggests that picrites are related to the basalts by fractional crystallisation. Initial radiogenic isotope ratios of the picrites have a restricted compositional range: ?_Nd=+6.1 to +6.6, ⁸⁷Sr/⁸⁶Sr=0.70296–0.70319; whereas the basalts display a wider range of compositions: ?_Nd=+6.6 to +7.6, ⁸⁷Sr/⁸⁶Sr=0.70321–0.70671. This variation in isotope ratios between basalts and picrites may be due to the assimilation of altered oceanic crust (or possibly partial melts of such crust) by a picritic magma along with fractional crystallisation. The relatively narrow range of Nd and Pb isotopic compositions in the Curaçao lavas suggests either that the source region was homogeneous, or that melts from a heterogeneous mantle source were well mixed before eruption. Chondritic to slightly light rare earth element enriched patterns, combined with long-term light rare earth element depletion (positive ?_Nd), suggest that the lavas were formed by polybaric melting of spinel lherzolite, with small a contribution from garnet lherzolite melts. High-MgO lavas, the absence of a subduction related chemistry, and the chemical similarity to other oceanic plateaux, suggest a mantle plume origin for the Curaçao lava succession. The Curaçao volcanic sequence is part of an oceanic plateau formed at about 88–90?Ma, fragments of which are dispersed around the Caribbean as well as being obducted onto the western margin of Colombia and Ecuador. The occurrence of high-Mg lavas throughout this Cretaceous Caribbean–Colombian igneous province requires anomalously hot mantle (>200^°?C hotter than ambient upper mantle) over a large part of a putative plume head, which is inconsistent with some mantle plume models.     

Origin and interaction of mafic and felsic magmas in an evolving late orogenic setting: the Early Paleozoic Terra Nova Intrusive Complex, Antarctica

The Abbott Unit (∼508 Ma) and the Vegetation Unit (∼475 Ma) of the Terra Nova Intrusive Complex (northern Victoria Land, Antarctica) represent the latest magmatic events related to the Early Paleozoic Ross Orogeny. They show different emplacement styles and depths, ranging from forcible at 0.4–0.5 GPa for the Abbott Unit to passive at ∼0.2 GPa for the Vegetation Unit. Both units consist of mafic, felsic and intermediate facies which collectively define continuous chemical trends. The most mafic rocks from both units show different enrichment in trace element and Sr-Nd isotopic signatures. Once the possible effects of upper crustal assimilation-fractional crystallisation (AFC) and lower crustal coupled AFC and magma refilling processes have been taken into account the following features are recognised: (1) the modelled primary Abbott Unit magma shows a slightly enriched incompatible element distribution, similar to common continental arc basalts and (2) the modelled primary Vegetation Unit magma displays highly enriched isotope ratios and incompatible element patterns. We interpreted these major changes in magmatic affinity and emplacement style as linked to a major change in the tectonic setting affecting melt generation, rise and emplacement of the magmas. The Abbott Unit mafic melts were derived from a mantle wedge above a subduction zone, with subcontinental lithospheric mantle marginally involved in the melting column. The Vegetation Unit mafic melts are regarded as products of a different source involving an old layer of subcontinental lithospheric mantle. The crustal evolution of both types of mafic melts is marked by significant compositional contrasts in Sr and Nd isotopes between mafic and associated felsic rocks. The crustal isotope signature showed an increase with felsic character. Geochemical variations for both units can be accounted for by a similar two-stage hybridisation process. In the first stage, the most mafic magma evolved mainly by fractional crystallisation coupled with assimilation of metasedimentary rocks having crustal time-integrated Sr and Nd compositions similar to those of locally exposed metamorphic basement. The second stage involves contaminated products mixing with independently generated crustal melts. Petrographic, geochemical and isotope data also provide evidence of significant compositional differences in the felsic end-members, pointing to the involvement of metaigneous and metasedimentary source rocks for the Abbott granite and Vegetation leucogranite, respectively. Received: 31 March 1998 / Accepted: 3 May 1999     

Strontium isotope systematics of Amba Dongar and Sung Valley carbonatite-alkaline complexes,India: evidence for liquid immiscibility,crustal contamination and long-lived Rb/Sr enriched mantle sources

The results of a Sr isotopic study of coexisting alkaline silicate rocks and carbonatites of two Cretaceous alkaline complexes of India, Amba Dongar (Deccan Flood Basalt Province) and Sung Valley (Rajmahal–Bengal–Sylhet Flood Basalt Province) are reported. The overlapping nature of initial Sr isotopic ratios of alkaline rocks and carbonatites of both the complexes is consistent with a magmatic differentiation model. Modelling of initial ⁸⁷Sr/⁸⁶Sr variation in alkaline rocks of Amba Dongar is consistent with a process of crustal assimilation by the parent magma undergoing simultaneous fractional crystallization of silicate rocks and silicate–carbonate melt immiscibility. A maximum of ∼5% crustal contamination has been estimated for the parent magma of Amba Dongar, the effect of which is not seen in the Sr isotope ratio of carbonatites generated by liquid immiscibility. A two point Rb–Sr isochron of the Sung Valley carbonatites, pyoxenite and a phlogopite from a carbonatite yielded an age of 106±11 Ma, which is identical to the ⁴⁰Ar–³⁹Ar age of this complex. The same age for the carbonatites and the alkaline silicate rocks, similar initial Sr ratios and the higher Sr concentration in the former than the latter favour the hypothesis of liquid immiscibility for the generation of the Sung Valley. The higher initial ⁸⁷Sr/⁸⁶Sr ratio for these complexes than that of the Bulk Earth indicates their derivation from long-lived Rb/Sr-enriched sources.     

Geochemistry of a transitional ne-trachybasalt — Q-trachyte lava series from Patmos (Dodecanesos), Greece: further evidence for fractionation,mixing and assimilation

Trace-element and preliminary Sr- and O-isotopic data are reported for a transitional alkaline-sub-alkaline lava series (MVS) from Patmos, Greece. The lava types belonging to this series are ne-trachybasalt, hy-trachybasalt, hy-trachyandesite and Q-trachyte. Rb, Sr and Ba contents, as well as K/Rb ratios, of the ne-trachybasalts differ from those of alkali basalts of oceanic islands and those of K-rich alkaline lavas of continental regions and are consistent with the occurrence of these volcanics in a destructive plate margin environment. Qualitatively, the variations shown by many trace elements throughout the MVS are explicable in terms of magma evolution via fractional crystallization involving removal of the observed phenocryst phases. Cross-cutting REE patterns can be explained by removal of small amounts of apatite. However, certain features of the data cannot be reconciled with the operation of fractional crystallization alone. These are: a) the compatible behavior of Ba throughout the MVS; b) the moderately (as opposed to highly) incompatible behavior of Zr, Rb and Nb relative to Th; and c) the significant decrease of K/Th, Rb/Th, Zr/Th, Zr/Nb, Nb/Th, Yb/Th, Ta/Th, U/Th and Zr/Ta ratios especially (but not exclusively) in the mafic part of the series. Quantitative modeling indicates that the hy-trachybasalts are anomalously enriched in both highly incompatible and highly compatible elements and these lavas are shown to be hybrids formed by mixing of ne-trachybasalt and hy-trachyandesite. Mixing proportions of the end members calculated from incompatible element abundances (19% ne-trachybasalt) differ from those calculated from compatible element abundances (62% ne-trachybasalt) and are inconsistent with proportions calculated from published mineral chemical data. In addition, mixing cannot account for the observed variations in incompatible element ratios and this is taken as evidence for the simultaneous operation of assimilation. Isotopic variations (⁸⁷Sr/ ⁸⁶Sr from 0.7049 to 0.7076 and ¹⁸O/¹⁶O from 4.7 to 8.6) and the positive correlation of isotope ratios with SiO₂ and Th contents provide conclusive proof that assimilation occurred. Calculations show that the isotopic characteristics and the concentrations of many trace elements in the Q-trachytes can be explained by fractional crystallization of ne-trachybasalt combined with assimilation of average continental crust (⁸⁷Sr/⁸⁶Sr-0.710), and that large amounts of assimilation are not necessary (Ma/Mc=0.55). REE data are not well explained by this model and suggest a crustal end-member enriched in LREE relative to the average crust. Zr and Hf data are also not well explained and indicate that the assimilant was depleted in HFSE relative to average crust or that HFSE are held back in relatively insoluble phases such as zircon in the restite during assimilation. Nevertheless, the results of the modeling demonstrate that Ba concentrations may decrease during AFC processes and that high Sr contents (1500 ppm in the MVS ne-trachybasalts) do not render mafic, parental magmas immune to the effects of assimilation in terms of their ⁸⁷Sr/⁸⁶Sr ratios. The results of this study confirm conclusions based upon major-oxide and mineral chemical data for the MVS lavas but, more importantly, show that careful analysis of trace element data allows the various processes involved in magma evolution to be identified and quantified, even in the absence of major oxide and isotopic data. Finally, it is reiterated that magma mixing and assimilation may be coupled processes in the magma chambers beneath many volcanic centers, and recognition of this fact has profound implications for studies of magmas erupted at continental margins and through continental crust.