USGS ScienceSearch

USGS · 70017603

Anatexis, hybridization and the modification of ancient crust: Mesozoic plutonism in the Old Woman Mountains area, California

Abstract

A compositionally expanded array of granitic (s.l.) magmas intruded the > 2 Ga crust of the Old Woman Mountains area between 160 and 70 Ma. These magmas were emplaced near the eastern (inland) edge of the Jurassic/Cretaceous arcs of western North America, in an area where magma flux, especially during the Jurassic, was considerably lower than to the west. The Jurassic intrusives and over half of the Cretaceous intrusives are predominantly metaluminous and variable in composition; a major Cretaceous suite comprises only peraluminous monzogranite. Only the Jurassic intrusions show clear evidence for the presence of mafic liquids. All units, including the most mafic rocks, reveal isotopic evidence for a significant crustal component. However, none of the Mesozoic intrusives matches in isotopic composition either average pre-intrusion crust or any major unit of the exposed crust. Elemental inconsistencies also preclude closed system derivation from exposed crust. Emplacement of these magmas, which doubled the volume of the mid- to upper crust, did not dramatically change its elemental composition. It did, however, affect its Nd and especially Sr isotopic composition and modify some of the distinctive aspects of the elemental chemistry. We propose that Jurassic magmatism was open-system, with a major influx of mantle-derived mafic magma interacting strongly with the ancient crust. Mesozoic crustal thickening may have led to closed-system crustal melting by the Late Cretaceous, but the deep crust had been profoundly modified by earlier Mesozoic hybridization so that crustal melts did not simply reflect the original crustal composition. The clear evidence for a crustal component in magmas of the Old Woman Mountains area may not indicate any fundamental differences from the processes at work elsewhere in this or other magmatic arcs where the role of pre-existing crust is less certain. Rather, a compositionally distinctive, very old crust may simply have yielded a more readily identifiable crustal fingerprint. The same processes that were involved here-mafic magma influx, hybridization, and remelting of hybridized crust-are likely to be typical of arc settings. ?? 1994.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

C. F. Miller, J. L. Wooden. 1994. Anatexis, hybridization and the modification of ancient crust: Mesozoic plutonism in the Old Woman Mountains area, California. https://doi.org/10.1016/0024-4937(94)90025-6

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

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

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

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