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42 records · Page 3Linked to original sources
USGS2018

Ore-forming adakitic porphyry produced by fractional crystallization of oxidized basaltic magmas in a subcrustal chamber (Jiamate, East Junggar, NW China)

Adakitic intrusions are supposed to have a close genetic and spatial relationship to porphyry Cu deposits. However, the genesis of adakitic intrusions is still under dispute. Here, we describe newly discovered intrusive complex rocks, which are composed of ore-bearing, layered magnetite-bearing gabbroic and adakitic rocks in Jiamate, East Junggar, NW China. These Jiamate Complex intrusions have diagnostic petrologic, geochronologic and geochemical signatures that indicate they were all generated from the same oxidized precursor magma source. Additionally, these layered rocks underwent the same fractional crystallization process as the ore-bearing adakitic rocks in the adjacent Kalaxiangar Porphyry Cu Belt (KPCB) in an oceanic island arc (OIA) setting. The rocks studied for this paper include layered magnetite-bearing gabbroic intrusive rocks that contain: (1) gradual contact changes between lithological units of mafic and intermediate rocks, (2) geochemical signatures that are the same as those found in oceanic island arc (OIA) rocks, (3) typical adakitic geochemistry, and (4) similar characteristics and apparent fractional crystallization relationships of ultra-basic to basic rocks to those in the nearby Beitashan Formation and to ore-bearing adakitic rocks in the KPCB. They also display similar zircon U-Pb and zircon Hf model ages. The Jiamate Complex intrusions contain intergrowths of magnetite and layered gabbro, and the intermediate-acidic intrusions of the Complex display typical adakitic affinities. Moreover, in conjunction with previously published geochronological and geochemistry data of the mafic rocks in the Beitashan Formation and in the KPCB area, additional data generated for the Jiamate Complex intrusions rocks indicate that they were formed from fractional crystallization processes. The Jiamate Complex intrusions most likely were derived from a metasomatized mantle wedge that was underplated at the root of the Saur oceanic island arc (Saur OIA). The ore-bearing adakitic intrusions in the KPCB and the adakitic Jiamate Complex intrusions were both probably generated from the same basaltic parental magmas through fractional crystallization. In addition, characteristics of the layered, magnetite-bearing, oxidized, basaltic Jiamate Complex intrusive rocks indicate that they are likely to be the parental arc magmas for the nearby porphyry Cu deposits. This conclusion is based on new interpretations of the regional and local geology, on interpretation of new geochemical analysis, new stable isotope analysis, new geothermobarometry, and new zircon age dating as well as other techniques and interpretations.

LITHOS↗
USGS2019

C–O stable isotope geochemistry and 40Ar/39Ar geochronology of the Bear Lodge carbonatite stockwork, Wyoming, USA

The carbonatite dike swarm and vein stockwork at the center of the Paleogene Bear Lodge alkaline complex (BLAC), Wyoming, USA, is host to diverse REE mineral assemblages that are largely a result of subsolidus modification and REE redistribution. Pseudomorphic replacement of primary burbankite by an assemblage of ancylite, strontianite, and barite is the result of interaction with late-stage hydrothermal fluids that added Sr, Ba, S, F, and REE, analogous to the replacement processes described for some carbonatite complexes of Russia's Kola Peninsula. Carbon and oxygen stable isotope ratios indicate that the primary carbonatite mineralogy experienced degassing/pneumatolysis and alteration by fluids of variable temperature, CO 2 /H 2 O ratios, and/or meteoric water content. Isotopic differences of matrix calcite between Group 1 carbonatites (avg. δ 13 C = −7.3‰; δ 18 O = 9.1‰) and Group 2 carbonatites (avg. δ 13 C = −9.9‰; δ 18 O = 10.2‰) are consistent with loss of CO 2 during degassing. The open-system alteration of burbankite caused a pronounced positive δ 18 O-shift in bulk ancylite pseudomorphs (δ 18 O: 14.3–25.7‰) relative to matrix calcite (δ 18 O: 8.7–11.2‰). Oxygen isotope compositions of biotite (δ 18 O: 4.5–5.9‰) and K-feldspar (δ 18 O: 7.3–7.9‰) in unoxidized carbonatite are typical of primary magmatic silicates and suggest that fluids responsible for the burbankite-to-ancylite conversion remained predominantly magmatic (carbohydrothermal). Concomitant increases toward the surface in 13 C and 18 O, oxidation, matrix carbonate dissolution, and the replacement of REE carbonates (ancylite, carbocernaite, and burbankite) by Ca-REE fluorocarbonates (bastnäsite, parisite, synchysite) suggest interaction with late-stage, low temperature (<250 °C) fluids characterized by lower CO 2 /H 2 O ratios, and an increasing meteoric water component. The first 40 Ar/ 39 Ar ages from carbonatite-hosted biotite and K-feldspar at the BLAC are between 51.45 ± 0.08 and 51.89 ± 0.14 Ma. Although carbonatite is commonly observed as the final intrusive phase in alkaline igneous complexes, relative-age relationships and previously published geochronology for Bear Lodge rocks indicate that alkaline silicate magmatism both preceded and followed carbonatite emplacement.

Wyoming↗
USGS2020

Timescales of magmatic processes in post-collisional potassic lavas, northwestern Tibet

Post-collisional potassic volcanic rocks on the Tibetan Plateau are widespread, but geologically young (<375 ka) volcanism suitable for 238 U- 230 Th geochronology is rare on the plateau. The geologically young Ashikule volcanic field from northern Tibet offers an excellent opportunity for studying high-resolution timescales of magmatism in continental collision zones. Here we report U-Th crystallization ages of zircons from Ashishan volcano and Wulukeshan volcano within the Ashikule volcanic field. In this study, we have identified 3 pulses of zircon crystallization at circa 70 ka, 105 ka, and 290 ka for Ashishan volcanic rocks and 1 pulse of zircon crystallization at circa 115 ka for Wulukeshan. Comparison of high-resolution zircon crystallization ages of 70 ka and 105 ka with respective eruption ages indicate that the zircon crystal residence time for the Ashishan volcano is short (<5 kyr). The presence of 290-ka zircon in a different Ashishan lava flow suggests the 270-ka volcanic pulse previously reported for other volcanoes in Ashikule volcanic field also occurred at Ashishan. The zircon crystallization age of ~115 ka for Wulukeshan volcano suggests that Wulukeshan volcano erupted later than previously inferred. Similar zircon age spectrums of ~105–115 ka for Ashishan and Wulukeshan volcanoes suggest a common interconnected subsurface magma reservoir for these two young volcanoes during Pleistocene time. Our new high-resolution U-Th zircon age data reveal that post-collisional potassic magmas below northern Tibet erupted soon after their formation (<5 kyr), in spite of their passage through thick continental crust. The high abundance (~60%) of geologically old (>375 ka) zircons demands for crystal-scale isotope studies of the widespread post-collisional lavas in continental collision zones, as the complexities cannot be resolved by bulk analysis methods alone.

LITHOS↗
USGS2025

Geochemistry and radiogenic isotopes constrain the mantle source region of the Mountain Pass Intrusive Suite, California

The Mountain Pass carbonatite stock is the largest rare earth element (REE) deposit and only active REE mine in the United States. The carbonatite intrusion and spatially associated alkaline silicate intrusions constitute the Mountain Pass Intrusive Suite, which is located within the Mojave Province in California. Both the carbonatite and the alkaline silicate rocks are enriched in large ion lithophile elements and light REEs, and less enriched to depleted in high field strength elements, indicating the mantle source region was metasomatically enriched in incompatible trace elements. The cause of this metasomatic mantle enrichment and the genetic relationship between the carbonatite and the alkaline silicate stocks are poorly understood. In this study, major and trace element geochemical data and isotopic (Rb-Sr, Sm-Nd, and Lu-Hf) data are presented to constrain genesis of the Mountain Pass Intrusive Suite, from mantle source region to the intrusion of the stocks. Our geochemical data are consistent with derivation of the alkaline silicate and carbonatite melts through partial melting from a shared mantle source region rather than through liquid immiscibility or fractional crystallization and separation of a carbothermal fluid. Although the Rb-Sr isotopic system in the Mountain Pass Intrusive Suite is disturbed at the whole-rock scale, the isotopic systems for whole-rock Sm-Nd (εNd i = ‐2.2 ± 0.8) and zircon Lu-Hf (εHf i = 0.1 ± 1.1) are robust and support mantle derivation of the magmas. Geochemical modeling using experimentally derived partition coefficients was used to identify possible causes of enrichment in incompatible elements through metasomatism in the mantle source region. Modeling of metasomatism by melts derived by partial melting of deeply subducted carbonated sediments approximates observed Mountain Pass Intrusive Suite trace element chemistry. Scattered εHf i in inherited zircon (2.8 ± 2.6) is consistent with derivation from an arc-related environment with substantial crustal contamination. Paleotectonic studies in the Mojave Province indicate that regional subduction preceded emplacement of the Mountain Pass Intrusive Suite by ∼300 Ma. Melting of the Mountain Pass source region may have been caused by post-collisional thermal relaxation and extension.

California↗
USGS1997

Late Paleozoic crustal history of central coastal Queensland interpreted from geochemistry of Mesozoic plutons: The effects of continental rifting

The eastern margin of Australia is understood to be the result of continental rifting during the Cretaceous and Tertiary. Consistent with this model, Cretaceous igneous rocks (granites to basalts) in a continental marginal setting near Bowen, Queensland are isotonically retarded, having isotopic ratios similar to those of most island arcs (Sri = 0.7030-0.7039, ??Nd = +6.46 to +3.00 and 206Pb/204Pb = 18.44-18.77, 207Pb/204Pb = 15.552-15.623, and 208Pb/204Pb = 37.90-38.52). These isotopic signatures are much less evolved than the Late Carboniferous-Permian batholith that many Cretaceous plutons intrude. As rocks ranging in age from about 300-100 Ma are well exposed near Bowen, we can track magma evolution through time. The significant change of magma source occurred much earlier than the Cretaceous based on the fact that Triassic granites in the same area are also isotonically primitive. We attribute the changes of magma composition to crustal rifting during the Late Permian and earliest Triassic. The Cretaceous rocks (actually latest Jurassic to Cretaceous, 145-98 Ma) themselves show compositional trends with time. Rocks of appropriate mineralogy for Al-in-hornblende geobarometry yield pressures ranging from 250 to 80 MPa for rocks ranging in age from 145 to 125 Ma, respectively. More significantly, this older group is relatively compositionally restricted, and is Sr-rich, and Y- and Zr-poor compared to 120-98 Ma rocks. This younger groups is bimodal, being comprised principally of basalts and rhyolites (granites). REE patterns for a given rock type, however, do not differ with age tribute these relatively subtle trace element differences to small differences in conditions (T, aH2O) at the site of melting. Cretaceous crustal rifting can explain the range of rock types and the spatial distribution of rocks < 120 Ma in a longitudinal strip between and overlapping with provinces of older Cretaceous intrusions. A subduction-related setting is assigned to the 145-125 Ma igneous rocks (those more than 50 Ma older than sea floor spreading). ?? 1997 Elsevier Science B.V.

LITHOS↗
USGS2000

Sr and Nd isotopic compositions, age and petrogenesis of A-type granitoids of the Vernon Supersuite, New Jersey Highlands, USA

Voluminous late Mesoproterozoic monzonite through granite of the Vernon Supersuite underlies an area of approximately 1300 km2 in the Highlands of northern New Jersey. The Vernon Supersuite consists of hastingsite ?? biotite-bearing granitoids of the Byram Intrusive Suite (BIS) and hedenbergite-bearing granitoids of the Lake Hopatcong Intrusive Suite (LHIS). These rocks have similar major and trace element abundances over a range of SiO2 from 58 to 75 wt.%, are metaluminous to weakly peraluminous, and have a distinctive A-type chemistry characterized by high contents of Y, Nb, Zr, LREE, and Ga/Al ratios, and low MgO, CaO, Sr and HREE. Whole-rock Rb-Sr isochrons of BIS granite yield an age of 1116 ?? 41 Ma and initial 87Sr/86Sr ratio of 0.70389, and of LHIS granite an age of 1095 ?? 9 Ma and initial 87Sr/86Sr ratio of 0.70520. Both suites have similar initial 143Nd/144Nd ratios of 0.511267 to 0.511345 (BIS) and 0.511359 to 0.511395 (LHIS). Values of ??(Nd) are moderately high and range from +1.21 to +2.74 in the BIS and +2.24 +2.95 in the LHIS. Petrographic evidence, field relationships, geochemistry, and isotopic data support an interpretation of comagmatism and the derivation of both suites from a mantle-derived or a juvenile lower crustal parent with little crustal assimilation. Both suites crystallized under overlapping conditions controlled by P-T-f(H(2)O). Lake Hopatcong magma crystallized at a liquidus temperature that approached 900??C and a pressure of about 6 kbar, and remained relatively anhydrous throughout its evolution. Initial P-T conditions of the Byram magma were ??? 850??C and about 5.5 kbar. BIS magma was emplaced contemporaneous with, or slightly preceding LHIS magma, and both magmas were emplaced during a compressional tectonic event prior to granulite facies metamorphism that occurred in the Highlands between 1080 and 1030 Ma. (C) 2000 Elsevier Science B.V. All rights reserved.

LITHOS↗