Hydration, 18O enrichment and oxidation during ocean floor hydrothermal metamorphism of ophiolitic metabasic rocks from E. Liguria,Italy

During ocean-floor hydrothermal metamorphism of a 225 m thick allochthonous Jurassic sequence of ophiolitic pillow lavas and underlying material in E. Liguria, Italy, the rocks were hydrated, enriched in ¹⁸O and oxidised. H₂O⁺ contents increased from ~0.3 to 3.8 wt.%, δ¹⁸O values increased from ~ +6‰ to values as high as +13.2‰, and ($\text{Fe}{}_2\text{O}{}_3\text{FeO}$1) increased from 0.18 to ratios as high as 1.0. Both δ¹⁸O values and oxidation ratios decrease in the original direction of increasing depth. Pillow margins are consistently more enriched in ¹⁸O and are more oxidised than cores.These observations are qualitatively interpreted in terms of a non-isothermal, heterogeneous reaction model of interaction of basalt with oxygen-bearing sea water during flow through the packed bed of pillows. Fluid flow approximated undirectional downward motion, and occurred in the recharge part of a cycle of single pass convection. Mass transfer through the pile was by flow (infiltration metasomatism), whereas intra-pillow mass transfer was diffusional. Oxygen isotope exchange and oxidation did not occur under conditions of perfect incremental equilibrium. An integrated bulk volumetric water/rock ratio of ~2 × 10³:1 is estimated from the oxidation profile.     

Rare-Earth Abundances in Basalts and Metabasalts from the Troodos Massif,Cyprus

Abundances of some rare-earth elements (REE) in twelve pillow lavas from the Upper Pillow Lavas and Axis Sequence of the Troodos Massif are reported. The samples consist of three fresh basalts and nine zeolite facies metabasalts, metamorphosed at temperatures between 0 and 200° C. All give similar light rare-earth element (LREE) depleted patterns, indicating that hydrothermal metamorphism within this temperature range does not appreciably affect these REE patterns. The LREE depletion is consistent with a petrogenetic model in which Troodos formed at a spreading axis. Variations in profile shape indicate that mantle melting beneath the axis may have taken place during a series of discrete episodes.     

Tectonics of the Troodos Massif (Cyprus): preliminary results

The core of the Troodos Massif consists of a major tectonitic harzburgite—dunite unit (Mt. Olympus Unit) overlain by three tectonic units which, in descending order, consist of dunites, wherlites and gabbros, respectively. Furthermore, the Mt. Olympus Unit is underlain by three other tectonic units with the same lithology as the upper ones. The thrusts show a north-to-south emplacement, probably of latest Cretaceous age.It is suggested that Troodos, Southern Turkey, Hatay and Oman ophiolites could belong to the same oceanic domain; they underwent different displacement toward the Arabian—African plate.     

Strontium isotopic equilibration during metamorphism of tillites from the Ogcheon Belt,South Korea

The NE/SW trending Ogcheon Belt formed during the Mesozoic by deformation and metamorphism of a sedimentary sequence which includes tillite formations of late Precambrian or Lower Palaeozoic age. In this study Rb-Sr isotopic data are reported from cm-scale sampling of clasts and matrix in these tillites, which underwent metamorphism at grades ranging from the biotite zone to the kyanite zone. Sr-isotopic disequilibrium between clasts and matrix persists up to the highest grade but in four out of five rocks the matrix samples approximate to isochrons (MSWD's<12). The mechanism for this selective isotopic equilibration is considered to be related to the metamorphic reactions in the matrix, which were probably accompanied by a substantial fluid flow. The matrix isochrons for three of the rocks, together with separated white micas from associated schists, suggest that metamorphism took place in the Trias, approximately 200 Myr ago. Metamorphism was followed by slow cooling and biotite closure temperatures were not reached until 190-150 Myr. — These results suggest that where high fluid/rock ratios can be demonstrated on independent petrological grounds, the analysis of small-scale whole-rock samples may allow effective Rb/Sr dating of metamorphism.     

O18 enriched ophiolitic metabasic rocks from E. Liguria (Italy), Pindos (Greece), and Troodos (Cyprus)

Low grade hydrothermally metamorphosed ophiolitic basic rocks from E. Liguria (Italy), Pindos (Greece) and Troodos (Cyprus) are enriched in O¹⁸ relative to the oxygen isotope ratio of fresh basalt (6.0±0.5‰). The maximum observed δO¹⁸ value of +13.22‰ corresponds to a positive isotope shift of 7‰ Enrichments in Sr⁸⁷ relative to Sr⁸⁶ correlate with hydrothermal alteration. The δC¹³ values of secondary calcite from E. Liguria are positive, and fall in the range from +0.2% to +3.6‰ Since ophiolitic rocks are considered to be fragments of the oceanic crust and upper mantle, and since the secondary metamorphic assemblages were produced before mechanical emplacement, it is considered that the hydrothermal metamorphism which affected these rocks occurred in the sub-sea-floor environment. The isotope data are directly consistent with the hypothesis that the alteration was produced by interaction of the basaltic material with introduced sea water. Water: rock ratios were sufficiently large to produce the observed isotope shifts. In the Troodos ophiolite sequence δO¹⁸ values decrease steadily downwards and change to progressively larger depletions in the Sheeted Intrusive Complex. The trend of δO¹⁸ decrease correlates with the original direction of increasing temperature. The O¹⁸ depletions, which have also been observed for oceanic “greenstones” (Muehlenbachs and Clayton, 1972b), resulted from water/rock interaction at temperatures greater than the particular temperature range above which whole rock-water fractionations became less than the isotopic difference between fresh basalt and sea water. Since this isotope geochemistry indicates that the water responsible for hydrothermal metamorphism was of sea water origin, the data support the more general hypothesis that convection of sea water within the upper 4–5 kms of the oceanic crust is a massive and active process at oceanic ridges. This process may be completely or partially responsible for (a.i.), the local scatter and low mean value of the conductive heat flux measured near ridges, (a.ii), the transfer of considerable quantities of heat from spreading oceanic ridges, (b) hydrothermal metamorphism, metasomatism and mineralization of oceanic crust, (c), the production of metal enriched, relatively reduced brines during sea water/basalt interaction, d), the high degree of scatter and low mean value of the compressional wave velocities of oceanic basement layer 2 and (e), the low natural remanent magnetization (NRM) intensity of the lower part of layer 2 and upper part of layer 3 of oceanic crust.     

Metabasalts from the Troodos Massif,Cyprus: Genetic implication deduced from petrography and trace element geochemistry

A wide variety of data support the contention that the Troodos massif, Cyprus is a fragment of oceanic lithosphere formed at a constructive margin some 85 m.y. ago. However, Troodos rocks differ significantly in major and trace element content and mineral parageneses from those formed at present day active constructive margins. It is here argued that the geochemical and petrographic characteristics of the massif are compatible with its formation at the axis of a slow spreading ridge within a small, marginal ocean basin.     

Petrological and Chemical Evolution of the Northeastern Troodos Extrusive Series, Cyprus

Four magma series are distinguished in the northeastern TroodosExtrusive Series: (A) a Lower Low-Ti Series (Lo-LTS) of basalticandesites, (B) a High-Ti Series (HTS) of basaltic andesitesto rhyodacites, (C) a Low-Ti Series(DLTS), the last two beingof basaltic andesite. Trace-element characteristics vary systematicallyfrom Series A to D and are interpreted in terms of a variablecontribution of three major source components (SCs). LILE-enrichedwater-rich fluids (SCI) derived from dehydration of a subductedlithosphere slab were continuously added to the overlying mantlewedge. Increasing LILE/HFSE and LILE/REE ratios and decreasingabsolute HFSE and REE concentrations from Series A to Dindicateprogressive depletion of the actual mantle source (SCII). Anegative Ta anomaly in the lavas decreases from Series A toD and is interpreted to have resulted from partial melting ofthe lower crust (SCII) where Ta-Nb-Ti may be fractionated byTi-rich accessory phases. The contribution of SCIII decreaseswhen the eruptive sites successively move away from the centralaxial zone and the temperature of the lower crust decreases,preventing partial melting of the lower crust. Chemical compositionsof fresh glass separates and phenocrysts indicate a change ofmajor petrogenetic processes from series A to D. Lo-LTS andIITS lavas are intrepreted to be directly related by open-systemfractional crystallization in crustal magma chambers. Removalof observed phenocryst phases clinopyroxene, orthopyroxene,plagioclase, and magnetite, and repeated subsequent mixing ofdacitc to rhyodacitic magmas with batches of replenshing basalticandesites are the major processes, possibly induced by vesicleformation in the mafic layer after a period of some crystallization.LTS and DLTS magmas were directly fed to the surface withoutstagnating at crustal levels, with feeder dykes positioned marginalto the central rift zone and thus by-passing the central magmachambers. These magmas apparently experienced only limited fractionalcrystallization of 10–15 wt.% olivine+clinopyroxene+chromite,probably at the mantle-crust boundary.     

Mass transfer during sub-seafloor alteration of the upper Troodos crust (Cyprus)

Five major alteration zones in the Extrusive Series and the Sheeted Dike Complex of the Troodos Ophiolite are each characterized by (a) distinct elemental changes compared to the original composition and (b) secondary mineralogy. The upper ca. 300 m of the extrusive crust, the highly oxidatedcold seawater alteration zone (CSA), is strongly enriched in K₂O and depleted in Na₂O. It is followed downwards by alow temperature alteration zone (<170° C) which is most widespread in the Troodos extrusives and where Na₂O and K₂O are enriched, the latter less strongly than in the CSA zone. Three types ofhigh temperature alteration zones (<440° C; HTA I–III) are found in the Sheeted Dike Complex. All are marked by thorough leaching of K₂O, while the behavior of Na₂O (e.g. unchanged in type III) and CaO (depleted in type I, enriched in types II, III) is variable. Mass budgets of elemental changes are quantified by calibration of whole rock analyses via systematic stable element variations of fresh glasses found throughout the extrusive section. The Troodos extrusive crust and upper Sheeted Dike Complex are a major sink for MgO, K₂O, and Na₂O, and a source for CaO; the overall scale of fluxes drastically exceeds estimates based on fresh basalt compositions from present ocean crust.     

Petrology and origin of primitive lavas from the Troodos ophiolite,Cyprus

Parental magmas to the Troodos ophiolite are characterised by low TiO₂ and Al₂O₃ and high SiO₂. Extremely fresh and chemically primitive (high MgO) rocks are found within the Upper Pillow Lavas and along the Arakapas Fault Belt of Cyprus and contain forsteritic olivine±enstatite and groundmass clinopyroxene set in glass or plagioclase, with accessory magnesiochromite and sometimes hornblende. They are quartz-normative and may have originally contained up to 3 wt% H₂O. Geochemically, there are three distinct groups of primitive lavas, based on TiO₂ and Zr contents but also reflected by CaO, Na₂O and REE abundances. These groups cannot be related by crystal fractionation and are considered to have been generated by incremental melting of a variably depleted source region. The parental magma to the least depleted group (Group I) was that of the major portion of the Troodos plutonic complex and is similar to those postulated for other low-Ti ophiolites. Chemically it has close affinities with komatiitic basalts. The most depleted lavas (Group III) all have U-shaped REE profiles and variable ¹⁴³Nd/ ¹⁴⁴Nd ratios, interpreted in terms of metasomatism of the source region by an incompatible element-enriched component which was probably derived from a subducted slab. These lavas represent an intermediate step in the development of boninite series rocks.     

High-pressure–low-temperature metamorphism of metasedimentary rocks, southern Menderes Massif, western Turkey

Kilometer-scale lenses of quartz-rich metasedimentary rocks crop out in a discontinuous belt along the southern margin of the Menderes Massif, Turkey, and preserve evidence for high-pressure–low-temperature (HP–LT) metamorphism related to subduction of a continental margin during Alpine orogeny. Kyanite schist, quartzite, and quartz veins contain kyanite + phengite + Mg-chlorite, and the veins also contain magnesiocarpholite. A deformed carbonate metaconglomerate juxtaposed with the quartzite-dominated unit does not contain HP index minerals, and likely represents the tectonized boundary of the siliceous rocks with adjacent marble. The HP–LT rocks (10–12 kbar, 470–570 °C) record different pressure conditions than the adjacent, apparently lower pressure Menderes metasedimentary sequence. Despite this difference there is disagreement as to whether these HP–LT rocks are part of the Menderes sequence or are related to the tectonically overlying Cycladic blueschist unit. If the former, the entire southern Menderes Massif experienced HP–LT metamorphism but the evidence has been obliterated from most rocks; if the latter, rocks recording different metamorphic-kinematic conditions experienced different tectonic histories and were tectonically juxtaposed during thrusting. Based on observations and data in this study, the second model better accounts for the differences in P–T-deformation histories of the southern Menderes Massif rocks, and suggests that the HP–LT rocks are not part of the Menderes cover sequence.     

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.     

Strontium isotopic studies of the volcanic rocks of the Saunda arc,Indonesia, and their petrogenetic implications

Pleistocene and Recent lavas from the Sunda arc range from those showing affinities with the island arc tholeiitic series, through a spectrum of calc-alkaline to high-K alkaline rocks. The tholeiitic rocks have relatively low ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios averaging 0–7043; the calc-alkaline rocks show a wide range (from 0.7038 to 0.7059, averaging 0.7048); the high-K alkaline rocks average 0.7045. A rhyolitic ignimbrite from Sumatra has an ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio of 0.7139.The relationship between ${}^{87}\text{Sr}{}^{86}\text{Sr}$ and major and trace element geochemistry is variable and complex. Lavas from the same volcano sometimes show significant differences in ${}^{87}\text{Sr}{}^{86}\text{Sr}$ despite close geochemical relationships. Rocks of the calc-alkaline suite show a regular decrease in ${}^{87}\text{Sr}{}^{86}\text{Sr}$ from West Java to Bali and there is some evidence for increasing ${}^{87}\text{Sr}{}^{86}\text{Sr}$ with increasing depth to the Benioff zone. Calc-alkaline and tholeiitic rocks from the Sunda arc have significantly higher ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios than those from other island arcs, except from those arcs where continental crustal involvement has been inferred (e.g. New Zealand).A model of ⁸⁷Sr enrichment due to isotopic equilibration of oceanic crust with sea water and disequilibrium melting in the slab and/or mantle is favoured to explain the Sr isotopic composition of the tholeiitic and normal calc-alkaline lavas. Calc-alkaline lavas with high ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios are best explained by either sialic contamination, or the presence of alkali basalt as a component of the downgoing slab. The Sr isotopic data for the high-K alkaline lavas suggest a mantle origin. The high ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio in the Lake Toba rhyolite implies a crustal origin.     

Strontium isotopic studies of alkalic rocks: Localities from Australia,Spain, and the Western United States

Initial Sr⁸⁷/Sr⁸⁶ ratios and rubidium and strontium contents have been measured in 83 specimens from 8 suites of alkalic and ultrabasic rocks. The range of initial Sr⁸⁷/Sr⁸⁶ ratio observed and the number of specimens (in parentheses) analysed for each suite are: West Kimberley, Australia (8), 0.7125–0.7215; Jumilla, Spain (6), 0.7136–0.7158; Bearpaw Mountains, Montana (9), 0.7062–0.7086; Highwood Mountains, Montana (10), 0.7072–0.7087; Hopi Buttes, Arizona (8), 0.7038–0.7094; Leucite Hills, Wyoming (17), 0.7055–0.7070; Montana diatremes (13), 0.7034–0.7073; Navajo Province, Arizona and New Mexico (12), 0.7052–0.7099.The initial Sr⁸⁷/Sr⁸⁶ ratios of the West Kimberley and Jumilla rocks are the highest yet found in strontium-rich basic rocks. Some of the individual specimens from West Kimberley have initial ratios as high as some estimates of the present Sr⁸⁷/Sr⁸⁶ ratio of average crustal material. This is interpreted to mean that the West Kimberley and Jumilla rocks contain substantial amounts of radiogenic strontium, and possibly other elements, from a crustal source.     

Middle Archean ocean ridge hydrothermal metamorphism and alteration recorded in the Cleaverville area, Pilbara Craton, Western Australia

A hydrothermally metamorphosed greenstone complex, capped by bedded cherts and banded iron formations (BIFs), is exposed in the Cleaverville area, Pilbara Craton, Western Australia. It has been interpreted as an accretionary complex characterized by both a duplex structure and an oceanic plate stratigraphy, and is shown to represent a 3.2 Ga upper oceanic crust. Three metamorphic zones are identified in the basaltic greenstones. The metamorphic grade increases from sub-greenschist facies (zones A and B) to greenschist facies (zone C) under low-pressure conditions. The boundaries between three mineral zones are subparallel to the bedding plane of overlying chert/BIF, and metamorphic temperature increases stratigraphically downward. The zones correspond to the thermal structure of ocean-floor metamorphism, at a mid-ocean ridge.
The uppermost greenstone in the study area is more pervasively altered and carbonatized than the modern upper oceanic crust. This indicates the enrichment of CO₂ in the metamorphic fluid by which widespread formation of carbonate occurred, compared with a narrow stability region of Ca-Al silicates. It is, therefore, suggested that the Archean hydrothermal alteration played a more important role in fixation of CO₂ than present-day ocean-ridge hydrothermal alteration, as an interaction between sea water and oceanic crust.     

A strontium,neodymium and oxygen isotope study of hydrothermal metamorphism and crustal anatexis in the Trois Seigneurs Massif,Pyrenees, France

Nd, Sr, and O isotope analyses have been made on metamorphic and igneous rocks and minerals from a 310–340 Ma Hercynian-age metamorphic terrane in the Pyrenees, France. Lower Paleozoic shales and phyllites have ⁸⁷Sr/⁸⁶Sr values of 0.707–0.717 at 310 Ma, but model values at 310 Ma of 0.709–0.736 (based on assumed depositional age of 450 Ma and an initial ⁸⁷Sr/⁸⁶Sr=0.707). On a regional scale, ⁸⁷Sr/⁸⁶Sr was homogenized to about 0.713 to 0.717 in the higher-grade pelitic schists during metamorphism. Much of this ⁸⁷Sr/⁸⁶Sr exchange occurred at very low grades (below the biotite isograd), but significant changes also accompanied the δ ¹⁸O lowering of the phyllites (+13 to +16) during their transformation to andalusite- and sillimanite-grade schists (δ ¹⁸O=+11 to +12); all of these effects are attributed to pervasive interactions with hydrothermal fluids (Wickham and Taylor 1985). The data also show that a syn-metamorphic plutonic complex, dominated by a biotite granite body, was derived by mixing of a relatively mafic magmatic end-member (⁸⁷Sr/⁸⁶Sr～ 0.7025–0.7050 and δ ¹⁸O～ +7.5 to +8.0) with two metasedimentary sources, both having ⁸⁷Sr/⁸⁶Sr～0.715 and δ ¹⁸O～ +10.0 to +12.0, but with one being more homogeneous than the other. The more homogeneous component and the (mantle-derived?) magmatic end-member dominate at low structural levels within the complex. The less homogeneous end-member that dominates at high levels is clearly derived from the local Paleozoic pelitic schists. A Rb-Sr age of 330±20 Ma was obtained on hornblende from a deep level within the complex, which fixes this age for the regional metamorphism, as well. Although a post-metamorphic granodiorite magma body at Trois Seigneurs also displays heterogeneities in δ ¹⁸O and ⁸⁷Sr/⁸⁶Sr (and thus does not give a clear-cut Rb-Sr isochron), the data are consistent with an emplacement age between 260 and 310 Ma, similar to ages of other late granodiorites in the Pyrenees. ¹⁴³Nd/ ¹⁴⁴Nd is very uniform within the Hercynian crust, both at Trois Seigneurs (? _Nd=?3 to ?7) and elsewhere in the Pyrenees; almost all igneous lithologies have depleted-mantle, mid-Proterozoic model ages, consistent with efficient recycling of crustal material following original crustal accretion in this area at about 1600 Ma or earlier. Rb-Sr mineral ages exhibit a complex cooling history reflecting late Hercynian and Mesozoic thermal events. Our results show that profound homogenization of the ⁸⁷Sr/⁸⁶Sr and ¹⁸O/¹⁶O ratios of large volumes of the crust can occur during regional metamorphism and crustal anatexis, particularly in regions undergoing extensional tectonics. Such processes can significantly modify the isotopic compositions of the protoliths of granitic magmas; this may explain why many peraluminous Hercynian granitoids of Western Europe have anomalously low (⁸⁷Sr/⁸⁶Sr) initial values compared to their probable sedimentary parent rocks.     

Pb−Sr−Nd isotopic behavior of deeply subducted crustal rocks from the Dora Maira Massif,Western Alps,Italy-II: what is the age of the ultrahigh-pressure metamorphism?

Pb, Nd and Sr isotope data are reported from two localities on mineral separates from Mg-rich metapelites and associated rocks that have been subducted to depths of at least 100 km, for which metamorphic conditions are estimated at 28–33 kilobars pressure and 700°–800° C, and then returned to the surface. Initial isotope ratio data from the granitoid country rock are similar to those found in the metapelites. The initial ratios indicate predominantly recycled, aged granitic crustal materials for the sources of all of the samples. Five zircon samples, 4 from pyrope megacrysts and 1 from fine-grained pyrope quartzite lenses in the metapelites accurately define a chord yielding intercept ages of 304±10 and 38.0±1.4 Ma in a concordia diagram. Zircon from the country rock also plots along the chord. The zircon data, together with initial Nd and Sr data, indicate that the sedimentary sources of the rocks were derived mainly or entirely from sialic Hercynian rocks. Ellenbergerite from pyrope megacrysts and monazite from the fine-grained ground mass yield slightly younger ages of 30–34 Ma, apparently reflecting lower blocking temperatures than that of zircon. Sm−Nd data from a pyrope megacryst give an errorchron corresponding to an age of 38 Ma, in agreement with the zircon date. A major question concerns the timing of the ultrahigh-pressure metamorphism. Experimental data suggest that pyrope and quartz/coesite as well as ellenbergerite formed by various metamorphic reactions. If, as generally assumed, the ultrahigh-pressure metamorphism occurred ca. 100 Ma ago, our data require that the zircon did not experience measurable lead loss at that time, but lost major amounts of lead 38 Ma ago during late Alpine metamorphism. Estimates of diffusion rates for Nd in pyrope further suggest that the apparent Sm/Nd age of 38 Ma for the megacryst is not consistent with that model. Those problems are resolved if the ultrahigh-pressure metamorphism occurred 38–40 Ma ago, but problems remain from Ar/Ar dates of 100 Ma on phengite, an inferred 120 Ma age for zircon lead loss from another study, and possibly by the very rapid uplift required if the metamorphism is that young. Dedicated to Professor Borwin Grauert on the occasion of his sixtieth birthday     

Constraints on the formation of geochemically variable plagiogranite intrusions in the Troodos Ophiolite,Cyprus

The geochemistry and petrology of tonalitic to trondhjemitic samples (n = 85) from eight different plagiogranite intrusions at the gabbro/sheeted dyke transition of the Troodos Ophiolite were studied in order to determine their petrogenetic relationship to the mafic plutonic section and the lava pile. The plagiogranitic rocks have higher SiO₂ contents than the majority of the glasses of the Troodos lava pile, but lie on a continuation of the chemical trends defined by the extrusive rocks, indicating that the shallow intrusions generally represent crystallised magmas. We define three different groups of plagiogranites in the Troodos Ophiolite based on different incompatible element contents and ratios. The first and most common plagiogranite group has geochemical similarities to the tholeiitic lavas forming the lavas and sheeted dyke complex in the Troodos crust, implying that these magmas formed at a spreading axis. The second plagiogranite group occurs in one intrusion that is chemically related to late-stage and off-axis boninitic lavas and dykes. One intrusion next to the Arakapas fault zone consists of incompatible element-enriched plagiogranites which are unrelated to any known mafic crustal rocks. The similarities of incompatible element ratios between plagiogranites, lavas and mafic plutonic rocks, the continuous chemical trends defined by plagiogranites and mafic rocks, as well as incompatible element modelling results, all suggest that shallow fractional crystallisation is the dominant process responsible for formation of the felsic magmas.