The tonalite–trondhjemite–granodiorite (TTG) to granodiorite–granite (GG) transition in the late Archean plutonic rocks of the central Wyoming Province

2006 ◽  
Vol 43 (10) ◽  
pp. 1419-1444 ◽  
Author(s):  
Carol D Frost ◽  
B Ronald Frost ◽  
Robert Kirkwood ◽  
Kevin R Chamberlain
Keyword(s):  
Rare Earth ◽  
Continental Crust ◽  
Rare Earth Element ◽  
Earth Element ◽  
Gradual Transition ◽  
Heavy Rare Earth Element ◽  
Isotopic Compositions ◽  
Similar Range ◽  
Wyoming Province ◽  
Ree Patterns

The 2.95–2.82 Ga quartzofeldspathic gneisses and granitoids in the Bighorn, western Owl Creek, and northeastern Wind River uplifts in the central Wyoming Province include low-K tonalite–trondhjemite–granodiorite (TTG) and high-K granodiorite–granite (GG) rocks. Both types of granitoids were intruded contemporaneously, although TTGs are more abundant in the older gneisses. The TTG suite consists of calcic to marginally calc-alkalic rocks that straddle the boundaries between metaluminous and peraluminous and between ferroan and magnesian compositions. Rare-earth element (REE) patterns of these rocks may be highly fractionated with low heavy rare-earth element (HREE) contents and modest to absent Eu anomalies but may also be less strongly HREE depleted. These rocks do not represent first-generation continental crust: most have unradiogenic Nd and radiogenic 207Pb/204Pb isotopic compositions that require the incorporation of isotopically evolved sources. The GG suite has compositions that are transitional between Archean TTG and modern, continental margin calc-alkalic rocks. The GG suite is characterized by higher alkali contents relative to CaO than the TTG suite and higher K/Na ratios but exhibits a similar range in REE patterns. The Nd, Sr, and Pb isotopic compositions of the GG suite are slightly less variable but lie within the range of those of the TTG suite. We interpret them as having a source similar to that of the TTG, perhaps forming by partial melting of preexisting TTG. The shift from TTG-dominated to GG-dominated continental crust was a gradual transition that took place over several hundred million years. Clearly subduction-related calc-alkalic magmatism is not recognized in the Wyoming Province prior to 2.67 Ga.

scholarly journals Trace Element and Stable Isotope Geochemistry of Lwamondo and Zebediela Kaolins, Limpopo Province, South Africa: Implication for Paleoenvironmental Reconstruction

Minerals ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 93
Author(s):  
Avhatakali Raphalalani ◽  
Georges-Ivo Ekosse ◽  
John Odiyo ◽  
Jason Ogola ◽  
Nenita Bukalo
Keyword(s):  
Trace Elements ◽  
Rare Earth ◽  
Stable Isotope ◽  
Trace Element ◽  
Continental Crust ◽  
Rare Earth Element ◽  
Earth Element ◽  
Paleoenvironmental Reconstruction ◽  
Δ18o And Δd ◽  
Ree Patterns

The aim of the present study was the paleoenvironmental reconstruction of the prevailing environment under which the Lwamondo and Zebediela kaolin deposits were formed. Hence, this study reports deuterium and oxygen stable isotope values and trace and rare earth element concentrations for two samples of kaolin. Upper continental crust-normalised trace-element patterns reveal that large ion lithophile elements and high-field-strength elements are generally depleted in Lwamondo and Zebediela kaolins, whereas transition trace elements are generally enriched in these kaolins. Upper continental crust-normalised rare earth element (REE) patterns show that there is a slight enrichment of heavy REEs (HREEs) compared to light REEs (LREEs) in these kaolins. The δ18O and δD stable isotope values for kaolinite from Lwamondo ranged from 17.4‰ to 19.1‰ and from −54‰ to 84‰, respectively, whereas those values for kaolinite from Zebediela varied from 15.6‰ to 17.7‰ and from −61‰ to –68‰ for δ18O and δD, respectively. The REE patterns and the content of other trace elements indicate ongoing kaolinitisation in the Lwamondo and Zebediela kaolins with minimum mineral sorting. The sources of the kaolins varied from basic to acidic and these were derived from an active margin tectonic setting. Lwamondo kaolin was deposited in an oxic environment whereas Zebediela kaolin was deposited under suboxic/anoxic conditions. Based on the δ18O and δD values of the kaolinite, they formed in a supergene environment at temperatures generally below 40 °C.

Rare-earth crystal chemistry of thalénite-(Y) from different environments

2018 ◽  
Vol 82 (2) ◽  
pp. 313-327
Author(s):  
Markus B. Raschke ◽  
Evan J. D. Anderson ◽  
Jason Van Fosson ◽  
Julien M. Allaz ◽  
Joseph R. Smyth ◽  
...  
Keyword(s):  
Rare Earth ◽  
Rare Earth Element ◽  
Earth Element ◽  
Spatial Scales ◽  
Structure Refinement ◽  
X Ray Diffraction ◽  
Heavy Rare Earth ◽  
Heavy Rare Earth Element ◽  
X Ray ◽  
Golden Horn

ABSTRACTThalénite-(Y), ideally Y3Si3O10F, is a heavy-rare-earth-rich silicate phase occurring in granite pegmatites that may help to illustrate rare-earth element (REE) chemistry and behaviour in natural systems. The crystal structure and mineral chemistry of thalénite-(Y) were analysed by electron microprobe analysis, X-ray diffraction and micro-Raman spectroscopy from a new locality in the peralkaline granite of the Golden Horn batholith, Okanogan County, Washington State, USA, in comparison with new analyses from the White Cloud pegmatite in the Pikes Peak batholith, Colorado, USA. The Golden Horn thalénite-(Y) occurs as late-stage sub-millimetre euhedral bladed transparent crystals in small miarolitic cavities in an arfvedsonite-bearing biotite granite. It exhibits growth zoning with distinct heavy-rare-earth element (HREE) vs. light-rare-earth element (LREE) enriched zones. The White Cloud thalénite-(Y) occurs in two distinct anhedral and botryoidal crystal habits of mostly homogenous composition. In addition, minor secondary thalénite-(Y) is recognized by its distinct Yb-rich composition (up to 0.8 atoms per formula unit (apfu) Yb). Single-crystal X-ray diffraction analysis and structure refinement reveals Y-site ordering with preferential HREE occupation of Y2 vs. Y1 and Y3 REE sites. Chondrite normalization shows continuous enrichment of HREE in White Cloud thalénite-(Y), in contrast to Golden Horn thalénite-(Y) with a slight depletion of the heaviest REE (Tm, Yb and Lu). The results suggest a hydrothermal origin of the Golden Horn miarolitic thalénite-(Y), compared to a combination of both primary magmatic followed by hydrothermal processes responsible for the multiple generations over a range of spatial scales in White Cloud thalénite-(Y).

Geology and geochemistry of Huronian rhyolites and low-Ti continental tholeiites from the Thessalon region, central Ontario

1987 ◽  
Vol 24 (7) ◽  
pp. 1360-1385 ◽  
Author(s):  
Wayne T. Jolly
Keyword(s):  
Rare Earth ◽  
Rare Earth Element ◽  
Earth Element ◽  
Magma Mixing ◽  
Mantle Metasomatism ◽  
Granitic Rocks ◽  
Heavy Rare Earth Element ◽  
Tonalitic Gneiss ◽  
Oceanic Basalts ◽  
Low K

Bimodal volcanism associated with early phases of Huronian rifting in central Ontario, dated about 2450 Ma, produced low-Ti tholeiitic basalts and two varieties of crustally derived calc-alkaline rhyolite. Early tholeiites are characteristically highly evolved, have Mg* values from 30 to 50, and display pronounced enrichment in large-ion lithophile elements (LILE) and light rare-earth element (LREE) in comparison with modern oceanic basalts, fractionated heavy rare-earth element (HREE) patterns, and low Ti, Zr, P, Nb, Ba, and K abundances. Ti/Zr ratios rise progressively in early basalts and associated basaltic andesite fractionates from about 35 in early flows to 55 in central units. Late basalts also carry enriched LILE and LREE, but, in contrast to early types, have average Mg* values greater than 50 and lower rare-earth element (REE) abundances with flat HREE patterns. They also display negative Ba, Nb, and P anomalies on chondrite-normalized distribution diagrams, but lack low K, Zr, and Ti contents. Their Ti/Zr ratios of about 80 approach chondritic levels. Melting models suggest the differences are explained by lower degrees of fusion (as low as 10%) in a hydrated, LILE- and LREE-enriched peridotite during generation of the early basalts, leaving a residue containing appreciable garnet, amphibole, Ti oxides, zircon, and apatite.Erupted simultaneously with the basalts were two distinctive rhyolite types: (1) a low-LILE, high-LREE group (25% of analysed specimens), derived by −20% melting of granulitic siliceous tonalitic gneiss, presumably at deep crustal levels, and (2) a high-LILE, low-LREE group (75%), derived, probably at shallower levels, by ≤ 30% melting in granitic rocks with pegmatitic or leucogranitic compositions. Mutual magma mixing of basalts and rhyolites during early stages of volcanism produced abundant hybrid andesites, but the frequency of contamination is much lower in later units.Hypothetical subcontinental source compositions, calculated from the Raleigh equation, suggest that the Huronian mantle had already undergone a complex history. Low Ba, Nb, P, Ti, and depleted HREE abundances compared with abundances for modern oceanic basalts suggest that a basaltic melt had already been withdrawn from this source during Archean time. Subsequently, an episode of hydrous metasomatism enriched the source in LILE and LREE. The latter event resulted from (1) subcontinental mantle metasomatism by previous Archean subduction, (2) mantle metasomatism during the terminal Archean Kenoran Orogeny, or (3) a wave of hydrous metasomatism accompanying Huronian mantle convection immediately preceding volcanism.

scholarly journals Petrogenesis of Heavy Rare Earth Element Enriched Rhyolite: Source and Magmatic Evolution of the Round Top Laccolith, Trans-Pecos, Texas

Minerals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 423 ◽  
Author(s):  
Brent Elliott
Keyword(s):  
Rare Earth ◽  
Rare Earth Element ◽  
Earth Element ◽  
Geochemical Evolution ◽  
Magmatic Differentiation ◽  
Magmatic System ◽  
Heavy Rare Earth ◽  
Heavy Rare Earth Element ◽  
Element Concentrations ◽  
Stage Crystallization

The Round Top rhyolite located in Trans-Pecos Texas is enriched in Be, F, Li, Nb, Rb, Sn, Th, U, Y, Zr, and rare earth elements (REEs). REE-bearing minerals are mainly ubiquitous nano-scale accessory phases throughout the groundmass, incorporated in synchysite-group minerals, xenotime-(Y), Y- and Ce-rich fluorite, and zircon. The rhyolite is peraluminous, high-silica, alkaline (not peralkaline), with elevated heavy rare earth element concentrations and anonymously negative Eu values. Pervasive spongy groundmass and recrystallization textures are consistent with the elevated and remobilized Zr, Th, and Y + HREE (heavy rare earth element) concentrations and a high field strength element (HFSE) soluble, sub-alkalic, F-rich, magmatic system. REE-bearing minerals are present as late-magmatic, interstitial phases and attributed with closed-system, post-magmatic, hydrothermal alteration. Petrogenetic modeling provides scenarios that explain the geochemical evolution and REE complexing behavior in evolved rhyolite magmas, and determines possible source compositions and evolution. Trace element models suggest a system typical of having extensive magmatic differentiation. The resulting rhyolite magma is indicative of a silica-rich magmatic system enriched in H2O, Li, and/or F that could be considered transitional between pure silicate melt and hydrothermal fluid, where fluorine-ligand complexing was prevalent through late magmatic cooling and crystallization processes. Thorough differentiation and high fluorine activity contributed to the late stage crystallization of REE-bearing minerals in the Round Top rhyolite.

Eocene Challis-Kamloops volcanism in central British Columbia: an example from the Buck Creek basin

1998 ◽  
Vol 35 (8) ◽  
pp. 951-963 ◽  
Author(s):  
J Dostal ◽  
D A Robichaud ◽  
B N Church ◽  
P H Reynolds
Keyword(s):  
British Columbia ◽  
Rare Earth ◽  
Rare Earth Element ◽  
Fractional Crystallization ◽  
Earth Element ◽  
Volcanic Rocks ◽  
Volcanic Belt ◽  
The United States ◽  
Calc Alkaline ◽  
Heavy Rare Earth Element

Eocene volcanic rocks of the Buck Creek basin in central British Columbia are part of the Challis-Kamloops volcanic belt extending from the United States across British Columbia to central Yukon. The volcanic rocks include two units, the Buck Creek Formation, composed of high-K calc-alkaline rocks with predominant andesitic composition, and the overlying Swans Lake unit made up of intraplate tholeiitic basalts. Whole rock 40Ar/39Ar data for both units show that they were emplaced at 50 Ma. They have similar mantle-normalized trace element patterns characterized by a large-ion lithophile element enrichment and Nb-Ta depletion, similar chondrite-normalized rare earth element patterns with (La/Yb)n ~4-14 and heavy rare earth element fractionation, and overlapping epsilonNd values (2.4-3.1) and initial Sr-isotope ratios ( ~ 0.704). These features suggest derivation of these two units from a similar mantle source, probably garnet-bearing subcontinental lithosphere. The differences between tholeiitic and calc-alkaline suites can be due, in part, to differences in the depth of fractional crystallization and the crystallizing mineral assemblage. Fractional crystallization of the calc-alkaline magmas began at a greater (mid-crustal) depth and included fractionation of Fe-Ti oxides. The volcanic rocks are probably related to subduction of the Farallon plate under the North American continent in a regime characterized by transcurrent movements and strike-slip faulting.

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