Geology topics

R. T. Gregory

Publications and source records attributed to R. T. Gregory.

4 recordsLinked to original sources

USGS2016

Cenozoic volcanic rocks of Saudi Arabia

The Cenozoic volcanic rocks of Saudi Arabia cover about 90,000 km 2 , one of the largest areas of alkali olivine basalt in the world. These volcanic rocks are in 13 separate fields near the eastern coast of the Red Sea and in the western Arabian Peninsula highlands from Syria southward to the Yemen Arab Republic. The initial phase of rifting of the Arabian Plate from the African Plate began as a wide zone of continental-crust extension manifested by basin and range topography. Freshwater lakes, northwest-trending marine gulfs, and alkali olivine basalt flows occupied these basins. Extensive dike swarms intruded parallel to the proto-Red Sea and marked the first phase of new mafic crust formed by volcanic processes. After a hiatus in volcanic activity, counterclockwise rotation of the Arabian Plate during middle Miocene time changed the stress pattern in the plate and a second phase of extrusion of alkali olivine basalt commenced along north-trending fractures. This stress pattern continues to influence Holocene volcanism. The earliest (pre-uplift) basalts to erupt on the Arabian Plate were predominantly undersaturated picrite and ankaramite, whereas those to erupt near the axis of the proto-Red Sea rift zone were tholeiite. The within-plate volcanic rocks evolved from picrite-ankaramite to alkali olivine basalt with minor volumes of fractionated, undersaturated felsic rocks. Continued crustal thinning and dike intrusion along the proto-Red Sea were accompanied by melting of the continental crust to produce silicic magma as part of a bimodal volcanic suite (tholeiite-rhyolite). These magmas were emplaced as dikes, sills, layered bodies, and flows that mark the early construction of the Red Sea crust. Second-phase lavas are predominantly fractionated hawaiites and alkali olivine basalts. Because undersaturated and oversaturated silicic magmas represent the second phase of activity, both fractional crystallization of the basaltic magma and melting of the crust are believed to have occurred. The historical record of volcanic activity in Saudi Arabia suggests that volcanism is dormant. The harrats should be evaluated for their potential as volcanic hazards and as sources of geothermal energy. The volcanic rocks are natural traps for groundwater; thus water resources for agriculture may be significant and should be investigated.

Open-File Report↗

USGS2010

Hydrogen and oxygen isotope constraints on hydrothermal alteration of the Trinity peridotite, Klamath Mountains, California

The Trinity peridotite represents a rare opportunity to examine a relatively fertile plagioclase peridotite that was exhumed and later subjected to intrusive events in a seafloor environment, followed by its emplacement and incorporation into a continent. Over 250 stable isotopic determinations on whole rocks and minerals elucidate the hydrothermal evolution of the Trinity complex. All three serpentine polymorphs are present in the Trinity peridotite; these separate on the basis of their δD values: antigorite, -46 < δD < -82‰ and lizardite and chrysotile, -90 < δD < -106 and -110 < δD < -136‰, respectively. Antigorite coexists with chlorite, talc, and tremolite in contact aureole assemblages associated with Silurian/Devonian gabbroic plutons. Lizardite and chrysotile alteration carries a meteoric signature, which suggests association with post-emplacement serpentinization, or overprinting of earlier low-temperature seafloor serpentinization. Regionally, contours of δD values exhibit bull's-eye patterns associated with the gabbroic plutons, with δD maxima coinciding with the blackwall alteration at the margins on the plutons. In contrast to the hydrogen isotope behavior, oxygen isotope values of the three polymorphs are indistinguishable, spanning the range 5.3 < δ 18 O< 7.5, and suggesting low integrated fluid fluxes and strongly 18 O-shifted fluids. Inferred primary δ 18 O values for peridotite, gabbro, and late Mesozoic granodiorite indicate a progressive 18 O enrichment with time for the source regions of the rocks. These isotopic signatures are consistent with the geology, petrochemistry, and geochronology of the Trinity massif, which indicate the following history: (1) lithospheric emplacement and cooling of the peridotite in an oceanic environment ~472 Ma; (2) intrusion of gabbroic plutons into cold peridotite in an arc environment between 435 and 404 Ma; and finally (3) intrusion of felsic plutons between 171 and 127 Ma, long after the peridotite was incorporated into the continental crust.

California↗

USGS1989

Oxygen isotope exchange kinetics of mineral pairs in closed and open systems: Applications to problems of hydrothermal alteration of igneous rocks and Precambrian iron formations

The systematics of stable-isotope exchange between minerals and fluids are examined in the context of modal mineralogical variations and mass-balance considerations, both in closed and in open systems. On mineral-pair ??18O plots, samples from terranes that have exchanged with large amounts of fluid typically map out steep positively-sloped non-equilibrium arrays. Analytical models are derived to explain these effects; these models allow for different exchange rates between the various minerals and the external fluids, as well as different fluid fluxes. The steep arrays are adequately modelled by calculated isochron lines that involve the whole family of possible exchange trajectories. These isochrons have initially-steep near-vertical positive slopes that rotate toward a 45?? equilibrium slope as the exchange process proceeds to completion. The actual data-point array is thus analogous to the hand of an "isotopic clock" that measures the duration of the hydrothermal episode. The dimensionless ratio of the volumetric fluid flux to the kinetic rate parameter ( u k) determines the shape of each individual exchange trajectory. In a fluid-buffered system ( u k ??? 1), the solutions to the equations: (1) are independent of the mole fractions of the solid phases; (2) correspond to Taylor's open-system water/rock equation; and (3) yield straight-line isochrons that have slopes that approach 1 f, where f is the fraction reacted of the more sluggishly exchanging mineral. The isochrons for this simple exchange model are closely congruent with the isochrons calculated for all of the more complex models, thereby simplifying the application of theory to actual hydrothermal systems in nature. In all of the models an order of magnitude of time (in units of kt) separates steep non-equilibrium arrays (e.g., slope ??? 10) from arrays approaching an equilibrium slope of unity on a ??-?? diagram. Because we know the approximate lifetimes of many hydrothermal systems from geologic and heat-balance constraints, we can utilize the 18O 16O data on natural mineral assemblages to calculate the kinetic rate constants (k's) and the effective diffusion constants (D's) for mineral-H2O exchange: these calculated values (kqtz ??? 10-14, kfeld ??? 10-13-10-12) agree with experimental determinations of such constants. In nature, once the driving force or energy source for the external infiltrating fluid phase is removed, the disequilibrium mineral-pair arrays will either: (1) remain "frozen" in their existing state, if the temperatures are low enough, or (2) re-equilibrate along specific closed-system exchange vectors determined solely by the temperature path and the mineral modal proportions. Thus, modal mineralogical information is a particularly important parameter in both the open- and closed-system scenarios, and should in general always be reported in stable-isotopic studies of mineral assemblages. These concepts are applied to an analysis of 18O 16O systematics of gabbros (Plagioclase-clinopyroxene and plagioclase-amphibole pairs), granitic plutons (quartz-feldspar pairs), and Precambrian siliceous iron formations (quartz-magnetite pairs). In all these examples, striking regularities are observed on ??-?? and ??-?? plots, but we point out that ??-?? plots have many advantages over their equivalent ??-?? diagrams, as the latter are more susceptible to misinterpretation. Using the equations developed in this study, these regularities can be interpreted to give semiquantitative information on the exchange histories of these rocks subsequent to their formation. In particular, we present a new interpretation indicating that Precambrian cherty iron formations have in general undergone a complex fluid exchange history in which the iron oxide (magnetite precursor?) has exchanged much faster with low-temperature (< 400??C) fluids than has the relatively inert quartz. ?? 1989.

Chemical Geology↗

USGS1987

Kinetic theory of oxygen isotopic exchange between minerals and water

Kinetic and mass conservation equations are used to describe oxygen isotopic exchange between minerals and water in "closed" and open hydrothermal systems. In cases where n coexisting mineral phases having different reaction rates are present, the exchange process is described by a system of n + 1 simultaneous differential equations consisting of n pseudo first-order rate equations and a conservation of mass equation. The simultaneous solutions to these equations generate curved exchange trajectories on ??-?? plots. Families of such trajectories generated under conditions allowing for different fluid mole fractions, different fluid isotopic compositions, or different fluid flow rates are connected by positive-sloped isochronous lines. These isochrons reproduce the effects observed in hydrothermally exchanged mineral pairs including 1) steep positive slopes, 2) common reversals in the measured fractionation factors (??), and 3) measured fractionations that are highly variable over short distances where no thermal gradient can be geologically demonstrated. ?? 1987.

Geochimica et Cosmochimica Acta↗