Trace element evidence for mantle heterogeneity beneath the Scottish Midland Valley in the Carboniferous and Permian

The alkaline rocks of Carboniferous to Permian age in the Midland Valley province range in composition from hypersthene-normative, transitional basalts to strongly undersaturated basanitic and nephelinitic varieties. They were formed by varying degrees of equilibrium partial melting of a phlogopite peridotite mantle. Ba, Ce, Nb, P, Sr and Zr were strongly partitioned into the liquid during melting; K and Rb were retained by residual phlogopite for small degrees of melting only. The composition of the mantle source is inferred to have been broadly similar to that from which oceanic alkaline basalts are currently being generated. It was, however, heterogeneous as regards distribution of the incompatible trace elements, with up to fourfold variations in elemental abundances and ratios. The mantle beneath the province may be divisible into several areas, of some hundreds of square kilometres each, which retained a characteristic incompatible element chemistry for up to 50 Ma and which imparted a distinctive chemistry to all the basic magmas generated within them.

F, Cl and Br contents of tholeiitic volcanic glasses dredged along the Mid-Atlantic Ridge from 53° to 28° N, including the transect over the Azores Plateau, are reported. The halogen variations parallel those of 87 Sr/ 86 Sr, La/Sm or other incompatible elements of varying volatility. The latitudinal halogen variation pattern is not obliterated if only Mg-rich lavas are considered. Variations in extent of low-pressure fractional crystallization or partial melting conditions do not appear to be the primary cause of the halogen variations. Instead, mantle-derived heterogeneities in halogens, with major enrichments in the mantle beneath the Azores, are suggested. The Azores platform is not only a ‘hotspot’ but also a ‘wetspot’, which may explain the unusually intense Azores volcanic activity. The magnitude of the halogen and incompatible element enrichments beneath the Azores appear strongly dependent on the size of these anions and cations, but independent of relative volatility at low pressure. The large anions Cl and Br behave similarly to large cations Rb, Cs and Ba, and the smaller anion F similarly to Sr and P. Processes involving crystal and liquid (fluid and/or melt), CO 2 rather than H 2 O dominated, seem to have produced these largescale mantle heterogeneities. Geochemical ‘anomalies’ beneath the Azores are no longer apparent for coherent element pair ratios of similar ionic size. Values of such ‘unfractionated’ coherent trace element ratios provide an indication of the mantle composition and its nature before fractionation event (s) which produced the inferred isotopic and trace element heterogeneities apparently present beneath the North Atlantic. The relative trace element composition of this precursor mantle does not resemble that of carbonaceous chondrites except for refractory trace element pairs of similar ionic size. It is strongly depleted in halogens, and to a lesser extent in large alkali ions Rb and Cs relative to refractory Ba. These relative depletions are comparable within a factor of 5 to Ganapathy & Anders’s estimates for the bulk Earth, with the exception of Cs. There is also evidence for removal of phosphorus into the iron core during its formation. With the exception of San Miguel, alkali basalts from the Azores Islands appear to have been derived from the same mantle source as tholeiitic basalts from the ridge transect over the Azores Platform but by half as much degree of partial melting. The Azores subaerial basalts seem to have been partly degassed in Cl, Br and F, in decreasing order of intensity. A working model involving metasomatism from release of fluids at phase transformation during convective mantle overturns is proposed to explain the formation of mantle plumes or diapirs enriched in larger relative to smaller halogen and other incompatible trace elements. The model is ad hoc and needs testing. However, any other dynamical model accounting for the 400 -1000 km long gradients in incompatible trace elements, halogens and radiogenic isotopes along the Mid-Atlantic Ridge should, at some stage, require either (1) some variable extent of mixing or (2) differential migration of liquid relative to crystals followed by re-equilibration (or both), as a diffusion controlled mechanism over such large distances is clearly ruled out, given the age of the Earth.


2021 ◽  
Author(s):  
Fernanda Torres Garcia ◽  
Mauricio Calderón ◽  
Leonardo Fadel Cury ◽  
Thomas Theye ◽  
Joachim Opitz ◽  
...  

<p>During the Upper Jurassic-Lower Cretaceous times the western margin of Gondwana in southern Patagonia experienced extreme lithospheric extension and generation of rift and marginal back-arc basins. The ophiolitic complexes of the Rocas Verdes basin comprises incomplete ophiolite pseudostratigraphy lacking ultramafic rocks. The Tortuga Ophiolitic Complex, the southernmost seafloor remnant of the Rocas Verdes basin, record the most advanced evolutionary stage of the back-arc basin evolution in a mid-ocean ridge-type setting. The base of the Tortuga Complex consists of massive and layered gabbros, most of which are two pyroxene and olivine gabbros, leucogabbros, and clinopyroxene troctolites intruded by dikes of basalt and diabase with chilled margins. We present new major and trace element composition of clinopyroxene from the gabbros and sheeted dikes complexes to assess the geochemical affinity of parental basaltic magmas. Clinopyroxene in gabbros is mostly augite and have Al contents of 0.06-0.14 a.p.f.u. and Mg# of 80-92. Clinopyroxene in dolerites in the sheeted dike unit (augite and diopside) have Al content of 0.11-0.12 a.p.f.u. and Mg# of 85-92. Some immobile trace elements (e.g. Zr, Ti, Y) are sensitive to the degree of partial melting and mantle source composition, and can be used as a proxy for distinguishing tectonic environments. The Ti+Cr vs. Ca diagram, coupled with moderate-high TiO<sub>2</sub> content of clinopyroxene (0.4-1.4 wt.%) suggests their generation in mid-oceanic ridge-type environment (cf. Beccaluva et al., 1989).  The high Ti/Zr ratios (of ~4-11) coupled with low Zr contents (~0.2-1.1) are expected for higher degrees of partial melting or for melting of more depleted mantle sources. Conversely, low Zr/Y ratios (0.05-0.13) plot between the range of arc basalts. Chondrite-normalized REE patterns in clinopyroxene display a strong depletion of LREE compared to HREE and have an almost flat pattern in the MREE to HREE with a positive Eu (Eu*= 0.9-1.1) anomaly, indicating that clinopyroxene crystallized from a strongly depleted mid-ocean-ridge-type basalt, formed by extensive fractional melting of the mantle source and/or fractional crystallization and accumulation of anhydrous phases. The general trend of the incompatible trace elements patterns exhibit depletion in LILEs, minor HFSEs depletion, positive anomaly of Rb and negative anomalies in Ba, Zr, Ti and Nb, consistent with their generation from a refractory mantle source barely influenced by subduction components derived from the oceanic slab. This agrees with basalt generation in a back-arc basin located far away from the convergent margin. This study was supported by the Fondecyt grant 1161818 and the Anillo Project ACT-105.</p>


1985 ◽  
Vol 122 (4) ◽  
pp. 389-396 ◽  
Author(s):  
R. S. Thorpe ◽  
R. Macdonald

AbstractThe Whin Sill comprises a major quartz tholeiite sill of late Carboniferous age underlying an area of c. 5000 km2 and with a volume of c. 200 km3, associated with contemporaneous dykes emplaced within Carboniferous sedimentary rocks in northeast England. New trace element analyses of chilled margins, sill interiors and dykes indicate that the Whin Sill complex magmas show significant chemical variations in terms of the relatively stable trace elements Th, Ce, Y, Zr, Nb and Ni. These data indicate that the complex was fed by a large number of compositionally distinct magma pulses, and that certain of the dykes may have formed feeder channels for the sill. The chemical characteristics of the sill and dyke samples are consistent with derivation by extensive polybaric fractional crystallization of olivine tholeiite magma derived by partial melting of compositionally heterogeneous mantle peridotite and/or crustal contamination of mantle-derived magmas.


1984 ◽  
Vol 75 (2) ◽  
pp. 259-273 ◽  
Author(s):  
W. E. Stephens ◽  
A. N. Halliday

ABSTRACTNew major- and trace-element data for granitoid plutons from the Grampian Highlands, the Midland Valley and the Southern Uplands of Scotland are presented and discussed. The study is restricted to ‘late granitoids’ (all younger than 430 Ma); the term ‘granitoid’ is used in a wide sense to encompass all plutonic components of a zoned intrusion of this age, sometimes including diorites and ultrabasic cumulate rocks. The data indicate that as a whole the province is chemically high-K calc-alkalic. Other notable enrichments are in Sr and Ba, and a marked geographical difference in these trace-elements is found between plutons of the SW Grampian Highlands and those of the Southern Highlands, the Midland Valley, and the Southern Uplands. Plutons of the NE Highlands tend to be more geochemically evolved than those further SW and those of the Midland Valley and Southern Uplands.When petrographical and geochemical data are considered, three plutonic suites are recognised: (1) the Cairngorm suite comprising plutons of the NE Highlands, (2) the Argyll suite comprising plutons from the SW Highlands, and (3) the S of Scotland suite comprising plutons from the Southern Highlands, Midland Valley and the Southern Uplands excluding Criffell and the Cairnsmore of Fleet. It is proposed that the more acidic granitoids are dominantly the products of I-type crustal sources, but certain diorites and the more basic members of zoned plutons have a substantial mantle component. The elevated Sr and Ba levels in granitoids of the Argyll suite may reflect the influence of incompatible-element-rich fluids from the mantle in the petrogenesis of this suite. The relatively anhydrous pyroxene-mica diorites of the S of Scotland suite are richer in Ni and Cr and appear to represent mantle-derived melts. The relationships between these data and already published isotopic data are discussed.


2020 ◽  
Author(s):  
Ercan Aldanmaz ◽  
Aykut Güçtekin ◽  
Özlem Yıldız-Yüksekol

<p>The Late Triassic basaltic rocks that are dispersed as several lava sheets in a number of different tectonic slices within the Antalya nappes in SW Turkey represent the remnants of widespread oceanic magmatism with strong intra-plate geochemical signatures. The largest exposures are observed around the Antalya Bay, where pillow structured or massif lava flows are interlayered with Upper Triassic pelagic or carbonate platform sediments. Based on bulk-rock geochemical characteristics, the rocks mostly classify as alkaline basalts and display distinctive OIB-type trace element distributions characterized by significant enrichments in LILE and HFSE abundances, as well as LREE/HREE ratios, with respect to average N-MORB. Quantitative modeling of trace element data suggest that the primary melts that produced the alkaline lavas are largely the products of variable proportions of mixing between melts generated by variable, but generally low (<10) degrees of partial melting of more than one compositionally distinct mantle source. The samples, as a whole, display large variations in radiogenic isotope ratios with <sup>87</sup>Sr/<sup>86</sup>Sr = 0.703021–0.70553, <sup>143</sup>Nd/<sup>144</sup>Nd = 0.51247–0.51279, <sup>206</sup>Pb/<sup>204</sup>Pb = 18.049–20.030, <sup>207</sup>Pb/<sup>204</sup>Pb = 15.544–15.723 and <sup>208</sup>Pb/<sup>204</sup>Pb = 38.546–39.530. Such variations in isotopic ratios correlate with the change in incompatible trace element relative abundances and reflect the involvement of a number of compositionally distinct mantle end-members. These include EMI and EMII type enriched mantle components both having lower <sup>143</sup>Nd/<sup>144</sup>Nd than typical depleted MORB source with their contrasting low and high <sup>206</sup>Pb/<sup>204</sup>Pb and <sup>20</sup><sup>7</sup>Pb/<sup>204</sup>Pb ratios respectively, as well as a high time-integrated <sup>238</sup>U/<sup>204</sup>Pb component with high <sup>206</sup>Pb/<sup>204</sup>Pb at relatively low <sup>87</sup>Sr/<sup>86</sup>Sr and εNd values. The results from trace element and radiogenic isotope data are consistent with the view that the initial melt generation was likely related to partial melting of the shallow convecting upper mantle in response to Triassic rifting events, while continued mantle upwelling resulted in progressively increased melting of mantle lithosphere that contained compositionally contrasting lithological domains with strong isotopic heterogeneities.</p>


2021 ◽  
Author(s):  
Lingquan Zhao ◽  
Sumit Chakraborty ◽  
Hans-Peter Schertl

<p>The Xigaze ophiolite (Tibet), which occurs in the central segment of the Yarlung Zangbo Suture Zone, exposes a complete portion of a mantle sequence that consists essentially of fresh as well as serpentinized peridotites. We studied a sequence beneath the crustal section that exposes fresh, Cpx-bearing harzburgites and dunites that are underlain by serpentinized Cpx-bearing harzburgites and dunites. The rocks at the bottom are crosscut by dykes that have undergone different degrees of rodingitization. The modal compositions of peridotite from both fresh and serpentinized sections plot in abyssal upper mantle fields, with clinopyroxene modes less than 5 vol. %. Although harzburgites and dunites indicate that melt has been lost relative to primitive mantle compositions, the trace element patterns carry signatures of enrichment in incompatible elements, such as (i) “bowl-shaped” patterns of trace elements in silicate-Earth normalized spider diagrams, (ii) positive anomalies in highly incompatible trace elements such as Rb, Th, U, Ta, and (iii) enrichment of LREE in the clinopyroxenes from dunites and harzburgites. These features are indicative of complex melt transfer processes and cannot be produced by simple melt extraction. Petrographic studies reveal that harzburgite and dunite contain interstitial polyphase aggregates of olivine + Cpx + spinel + Opx and olivine + Cpx + Spinel, respectively. Experimental studies (e.g. Morgan and Liang, 2003) suggest that these aggregates represent frozen melt-rich components, indicating that fertile melt was percolating through the depleted harzburgite – dunite matrix. Presence of such “melt pods” would explain the trace element enrichment patterns of the bulk rock, as well as features such as reverse zoning (core: Cr, Fe<sup>2+</sup> rich, rim: Al, Mg rich) of spinels in polyphase aggregates in fresh dunites. These results show that melt extraction from the mantle is not a single stage process, and that evidence of multiple melt pulses that propagated through a rock are preserved in the petrographic features as well as in the form of chemical signatures that indicate refertilization of initially depleted rocks.</p>


1994 ◽  
Vol 58 (391) ◽  
pp. 205-214 ◽  
Author(s):  
J. V. Owen ◽  
J. Dostal ◽  
B. N. Church

AbstractMetasomatic interaction on a cm scale between calc-silicate pods and the enclosing sillimanite + biotite + tourmaline gneiss at Partridge Breast Lake, northern Manitoba, Canada, led to the development of an inner (by calc-silicate rock), hornblende-rich reaction zone and an outer, biotite-rich zone. The boundary between the reaction zones is interpreted as the original calc-silicate/metapelite interface. Compared with its metapelitic protolith, the biotite zone shows a two- to twenty-fold depletion in the concentrations of incompatible trace elements (notably the light rare earths, U, Th, Nb, Ta, Zr and Hf). In contrast, the relative concentrations of trace elements remained nearly constant during the mineralogical transformation of the calc-silicate rock to the hornblende zone. The depletion of trace elements in the biotite zone is attributed to the dissolution of accessory phases (e.g. monazite). Although stable at the metamorphic conditions (∼600–650°C at ∼ 4.5 kbar) prevalent during metasomatism, Mg-rich tourmaline is absent in the biotite zone, suggesting that either the pH or composition (e.g. the (Al + Si)/(Ca + Mg + Fe) ratio) of the aqueous fluid phase was inappropriate for the preservation of this mineral.


2019 ◽  
Vol 60 (12) ◽  
pp. 2483-2508 ◽  
Author(s):  
R Tribuzio ◽  
G Manatschal ◽  
M R Renna ◽  
L Ottolini ◽  
A Zanetti

Abstract The Jurassic Chenaillet ophiolite in the Western Alps consists of a gabbro–mantle association exhumed to the seafloor through detachment faulting and partly covered by basaltic lavas. One of the Chenaillet gabbroic bodies includes mylonites that are transected by a network of felsic veins, thereby testifying to the interplay of ductile shearing and magma emplacement. The deformed gabbros preserve clinopyroxene porphyroclasts of primary magmatic origin, which are typically mantled by amphibole (titanian edenite) and minor secondary clinopyroxene. Titanian edenite and secondary clinopyroxene also occur as fine-grained syn-kinematic phases locally associated with fine-grained plagioclase. The felsic veins are made up of anorthite-poor plagioclase and minor titanian edenite. Geothermometric investigations document that the ductile gabbro deformation and the crystallization of the felsic veins occurred at 765 ± 50 °C and 800 ± 55 °C, respectively. With respect to undeformed counterparts, the deformed gabbros are variably enriched in SiO2 and variably depleted in Mg/(Mg + Fetot2+) and Ca/(Ca + Na). In addition, the deformed gabbros show relatively high concentrations of incompatible trace elements such as rare earth elements (REE), Y, Zr and Nb. The felsic veins are characterized by low Mg/(Mg + Fetot2+) and Ca/(Ca + Na), high SiO2 and high concentrations of incompatible trace elements. Relict clinopyroxene porphyroclasts from the deformed gabbros display a rather primitive, mid-ocean ridge-type geochemical signature, which contrasts with the trace element fingerprint of titanian edenite from both the deformed gabbros and the felsic veins. For instance, titanian edenite typically has relatively high REE abundances, with chondrite-normalized REE patterns characterized by a pronounced negative Eu anomaly. A similar trace element signature is shown by secondary clinopyroxene from the deformed gabbros. Amphibole from both the deformed gabbros and the felsic veins displays high F/Cl values. We show that the SiO2-rich hydrous melts feeding the felsic veins were involved in the high-temperature gabbro deformation and that melt–gabbro reactions led to major and trace element metasomatism of the deforming gabbros.


2019 ◽  
Vol 124 (7) ◽  
pp. 6490-6503
Author(s):  
Yanfei Zhang ◽  
Chao Wang ◽  
Lüyun Zhu ◽  
Zhenmin Jin ◽  
Wei Li

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