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Geology topics

R. G. Coleman

Publications and source records attributed to R. G. Coleman.

At least 19 recordsLinked to original sources

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

Tectonic setting for ophiolite obduction in Oman

The Samail ophiolite is part of an elongate belt in the Middle East that forms an integral part of the Alpine mountain chains that make up the northern boundary of the Arabian-African plate. The Samail ophiolite represents a portion of the Tethyan ocean crust formed at a spreading center of Middle Cretaceous age (Cenomanian). During the Cretaceous spreading of the Tethyan Sea, Gondwana Land continued its dispersal, and the Arabian-African plate drifted northward about 10°. These events combined with the opposite rotation of Eurasia and Africa initiated the closing of the Tethyan during the Late Cretaceous. At the early stages of closure, downwarping of the Arabian continental margin combined with the compressional forces of closure from the Eurasian plate initiated obduction of the Tethyan oceanic crust along preexisting transform faults, and still hot oceanic crust was detached along oblique northeast dipping thrust faults. Amphibolites developed at the base of the detached hot peridotite as it was thrust southward over oceanic volcanic and sedimentary rocks. Plate configurations combined with palinspastic reconstructions show that subduction and attendant large-scale island arc volcanism did not commence until after the Tethyan sea began to close and after the Samail ophiolite was emplaced southward across the Arabian continental margin. The Samail ophiolite nappe now rests upon a melange consisting mainly of pelagic sediments, volcanics, and detached fragments of the basal amphibolites which in turn rest on autochthonous shelf carbonates of the Arabian platform. Laterites and conglomerates with reworked laterites on the eroded upper surface of the ophiolite indicate a period of emergence prior to the deposition of shallow water Maestrichtian carbonates. Following emplacement (Eocene) of the Samail ophiolite, the Tethyan oceanic crust began northward subduction, and active arc volcanism started just north of the present Jaz Murian depression in Iran.

Journal of Geophysical Research Solid Earth

The crustal structure from the Altai Mountains to the Altyn Tagh fault, northwest China

[1] We present a new crustal section across northwest China based on a seismic refraction profile and geologic mapping. The 1100‐km‐long section crosses the southern margin of the Chinese Altai Mountains, Junggar Accretional Belt and eastern Junggar basin, easternmost Tianshan Mountains, and easternmost Tarim basin. The crustal velocity structure and Poisson's ratio (σ), which provide a constraint on crustal composition, were determined from P and S wave data. Despite the complex geology, the crustal thickness along the entire profile is nearly uniform at 50 km. The thickest crust (56 km) occurs at the northern end of the profile beneath the Altai Mountains and the thinnest (46 km) crust is beneath the Junggar basin. Beneath surficial sediments, the crust is found to have three layers with P wave velocities ( V p ) of 6.0–6.3, 6.3–6.6, and 6.9–7.0 km/s, respectively. The southern half of the profile, including the eastern Tianshan Mountains and eastern margin of the Tarim basin, shows low P wave velocities and σ = 0.25 to a depth of 30 km, which suggests a quartz‐rich, granitic upper crustal composition. The northern half of the profile below the Altai Mountains and Junggar Accretional Belt has a higher Poisson's ratio of σ = 0.26–0.27 to a depth of 30 km, indicative of an intermediate crustal composition. The entire 1100‐km‐long profile is underlain by a 15–30 km thick high velocity (6.9–7.0 km/s; σ = 0.26–0.28) lower‐crustal layer that we interpret to have a bulk composition of mafic granulite. At the southern end of the profile, a 5‐km‐thick midcrustal low‐velocity layer ( V p = 5.9 km/s, σ = 0.25) underlies the Tianshan and the region to the south, and may be indicative of a near‐horizontal detachment interface. P n velocities are ∼7.7–7.8 km/s between the Tianshan and the Junggar basin, and ∼7.9–8.0 km/s below the Altai Mountains and eastern margin of the Tarim basin. We interpret the consistent three‐layer stratification of the crust to indicate that the crust has undergone partial melting and differentiation after Paleozoic terrane accretion. The thickness (50 km) of the crust appears to be related to compression resulting from the Indo‐Asian collision.

Altai Mountains

Geochronology of the Arabian Shield, western Saudi Arabia: K-Ar results

An orogenic event, correlated with the Pan-African event in eastern Africa, affected the Arabian Peninsula between 510 and 610 m.y. ago and is well-recorded geochronologically. The event probably included two thermal pulses or maxima, the first occurring between 560 and 610 m.y. ago and the second between 510 and 540 m.y. ago. The earlier pulse, the more severe one, included the majority of the igneous activity and metamorphism. During the last part of the 510- to 610-m.y. period, left-lateral strike-slip faulting occurred along a set of northwest-trending en echelon fracture zones, whose composite displacement may be as large as 240 km. At least one and probably more orogenic events affected the Arabian Peninsula before the Pan-African event, but only minimum ages can be assigned to these, because thermal effects of the 510- to 610-m.y. event have reset K-Ar ages. Major diorite-granite batholiths, however, formed before 760 m.y. ago.

Arabian Shield

Sr87/Sr86, K, Na, Rb, and Sr in some eclogites and associated basalts from California and southwestern Oregon

Six samples of group C eclogites from California and southwestern Oregon have initial Sr 87 /Sr 86 ratios in the range of 0.7028 to 0.7051; Rb contents from less than 1 to 53.4 ppm; and Sr contents from 147 to 270 ppm. These data and major-element compositions suggest that the eclogites were derived from basalts older than but similar in composition to those intercalated with Mesozoic cugeosynclinal sedimentary rocks in California and western Oregon. The isotopic heterogeneity of the eclogites and associated graywackes contrasts with a uniformity of Sr 87 /Sr 86 in many younger calc-alkaline volcanic rocks of the circum-Pacific province. Derivation of the younger volcanic rocks from an eclogite-blueschist melange isotopically similar to those investigated here would require isotopic homogenization or integrated partial melting over sufficient volumes so as to reduce these variations in the derived melts.

California, Oregon

Structure and petrology of the alpine-type peridotite at Burro Mountain, California, U.S.A.

The alpine-type peridotite at Burro Mountain is a partially serpentinized harzburgite-dunite body approximately 2 km in diameter. It lies in a chaotic mélange derived from the Franciscan Formation (Upper Jurassic to Upper Cretaceous) of the southern Coast Ranges of California. The peridotite is bounded on the east by a vertical fault in the Nacimiento fault zone that brings sedimentary rocks of Taliaferro's (1943 b ) Asuncion Group (Upper Cretaceous) into contact with the peridotite. The peridotite appears to be one of a number of tectonic lenses, having a wide range in size, that make up the mélange . These lenses include metagraywacke, metachert, greenstone, amphibolite, and blueschist, as well as ultramafic rocks, and represent a wide range of pressure-temperature environments. The outer shell of the peridotite is a sheared serpentinite zone 10–15 m thick. The peridotite was tectonically emplaced at its present level as a cold solid mass and had little effect on the mineral assemblages of the Franciscan Formation. Local development of lawsonite and aragonite in shear zones may be related to the peridotite emplacement. Foliated harzburgite forms approximately 60 per cent of the peridotite. It is a lithologically uniform rock that has an olivine: orthopyroxene ratio of approximately 75:25. Accessory clinopyroxene and chromian spinel generally make up less than 5 per cent of the harzburgite. Dunite, composed of olivine, accessory chromian spinel (< 5 per cent), and trace amounts of pyroxene, makes up approximately 40 per cent of the peridotite and occurs as dikes, sills, and irregular bodies in the harzburgite. Olivine and pyroxene show small but significant compositional variations and chromian spinel shows a large range in the cation ratio Cr/(Cr+Al+ Fe 3+ ). The compositional variations in these minerals are related to original differences in bulk chemical composition. The following compositional ranges were determined for minerals in the harzburgite: olivine, Fo 91.1 −Fo 91.4 ; orthopyroxene, En 89.8 −En 91.1 ; clinopyroxene, Ca 47.0 Mg 50.0 Fe 3.0 −Ca 48.7 Mg 48.2 Fe 3.1 ; chromian spinel, Cr/(Cr+Al+Fe 3+ ) 0.37−0.55. The pyroxenes have a range in A1 2 O 3 content of 1.3−3.0 wt per cent. Olivine from dunite ranges from Fo 91 to Fo 92 7 and the chromian spinel has a range in the Cr/(Cr+Al+Fe 3+ ) ratio of 0.30−0.75. Although all the dunites are lithologically similar, three distinct types are recognized on the basis of composition of coexisting olivine and chromian spinel. Structural relations between the three types of dunite suggest three periods of emplacement (possibly overlapping) of dunite into harzburgite. The evidence indicates that the dunite, and probably also the harzburgite crystallized from an ultramafic magma, probably in the upper mantle. After the magmatic episode and crystallization, the peridotite was subjected to a deep-seated plastic deformation and recrystallization. The first phase of the deformation produced a pervasive, planar structural element (S 1 ) that crosscuts many harzburgite-dunite contacts. It is probable that some of the dunite sills were emplaced during this deformation. The foliation, S 1 , is defined by layers of different orthopyroxene content in harzburgite, and by discontinuous layers of chromian spinel in dunite. Flow or slip along S 1 produced slip folds in harzburgite—dunite contacts with axial planes parallel to S 1 . At a later stage, isoclinal folds developed in S 1 , and the present olivine microfabric was probably formed by recrystallization in the stress field that produced the isoclinal folding. In the olivine microfabric, X tends to be perpendicular to the axial planes (S 2 ) of the isoclinal folds and Y and Z tend to form double maxima in S 2 approximately 90° apart. Mg−Fe 2+ distribution between coexisting mineral pairs yields a calculated temperature of formation of approximately 1200 °C. Although this temperature is only a nominal value, it indicates that the mineral pairs equilibrated at a significantly high temperature. In view of the deformation and recrystallization, the calculated temperature possibly represents subsolidus re-equilibration of the minerals during this event. The deformation and recrystallization probably occurred shortly after crystallization while the peridotite was still at a high temperature. A later deep-seated deformation produced small scattered kink folds in S 1 that tend to disrupt the major olivine microfabric. The kink folding was accompanied or followed by the development of kink bands in olivine that reflect intragranular gliding on the system T = [ Okl ], t = [100]. The kink bands probably formed at a minimum temperature of 1000 °C. Following the deep-seated deformation, which probably took place in the mantle, the peridotite mass was tectonically detached and moved upward to its present level in the crust. Cleavages, joints, and faults provided channels for water to pervade the peridotite and allow alteration of the primary minerals.

California

A chemical study of serpentinization — Burro Mountain, California

Serpentinized dunites and harzburgites from the Burro Mountain peridotite show no change in the ratio of iron and magnesia to silica when compared with the same ratio for the unserpentinized equivalents. The mineral assemblage resulting from serpentinization consists of lizardite-chrysotile, brucite, and magnetite and is determined by the original bulk composition of the peridotite. The chemical and mineralogical data indicate that serpentinization proceeded under isochemical conditions except for the introduction of water into the peridotite. Expansion accompanies serpentinization because the serpentine products occupy a greater volume than the peridotite protolith. Tectonic emplacement of the Burro Mountain peridotite was facilitated by serpentinization and the attendant expansion.

California

Distribution and age of high-grade blueschists, associated eclogites, and amphibolites from Oregon and California

Isolated blocks of high-grade blueschist and amphibolite facies metamorphic rocks occur within the Jurassic and Cretaceous eugeosynclinal deposits of the Coast Ranges of southwestern Oregon and California. The blocks range in size from individual rock masses commonly 5 to 1,000 ft in diameter to a few larger masses as much as 7 mi long and 2 mi wide. The high-grade blocks are predominantly basaltic in composition and include glaucophane schists, eclogites, and gneissic rocks of the amphibolite facies. Field relationships indicate that the blocks are closely associated with serpentine, that high-grade blueschist and amphibolite blocks, lower grade blueschists, volcanic rocks, and cherts occupy disturbed zones that may be related to thrusting, and that there is no exposed in situ provenance for the high-grade blueschists, eclogites, and amphibolites. Potassium-argon mineral ages of white mica and actinolite from the blueschists and of hornblende from the amphibolites indicate that these minerals crystallized approximately 150 m.y. ago, but the ages measured on glaucophane from the blueschist blocks are commonly younger. These data suggest that the high-grade blue-schist and amphibolite blocks represent fragments of a cryptic metamorphic terrane of pre-Tithonian age that have been tectonically mixed with younger rocks of the Franciscan Formation in California and Otter Point Formation in Oregon. The younger ages for glaucophane probably reflect metamorphic episodes in which lower grade in situ blueschist facies mineral assemblages were developed in the blocks after their emplacement within the Franciscan Formation. This pre-Tithonian cryptic metamorphic terrane probably developed as a result of interaction between oceanic and continental plates. The occurrence of tectonic blocks of this terrane within mélange zones in Oregon and California may be related to later plate interaction.

California, Oregon

Blueschist-facies metamorphism related to regional thrust faulting

Rocks of the blueschist (glaucophane schist) facies occur throughout the world in narrow tectonic belts associated with ultramafic rocks. In the Coast Range province of California, blueschist rocks are devloped in the eugeosynclinal Franciscan Formation of Late Mesozoic age. The blueschist rocks form a narrow belt for more than 800 km along the eastern margin of this province and commonly are separated from rocks of an overlying thrust plate by serpentinite. Increasing metamorphism upward toward the thrust fault is indicated mineralogically by a transition from pumpellyite to lawsonite and texturally by a transition from metagraywacke to schist. The blueschist metamorphism probably occurred during thrusting in a zone of anomalously high water pressure in the lower plate along the sole of the thrust fault. This tectonic mode of origin for blueschist differs from the generally accepted hypothesis involving extreme depth of burial. Other belts of blueschist-facies rocks, including the Sanbagawa belt of Japan, the marginal synclinal belt of New Zealand, and the blueschist-ultramafic belts of Venezuela, Kamchatka, Ural mountains, and New Caledonia have similar geologic relations and might be explained in the same manner.

Tectonophysics

Alkali amphiboles from the blueschists of Cazadero, California

Alkali amphiboles from Type III and Type IV metamorphic zones in blueschist facies rocks of Cazadero, California, and from comparable New Caledonian rocks have been characterized by X-ray crystallographic, optical, and chemical methods. The composition of any particular alkali amphibole is strongly controlled by the bulk composition of the host rock. Within the blueschist facies, metamorphic zones are not characterized by changes in amphibole composition. All the alkali amphiboles studied herein belong to the C2/m space group and complete miscibility between glaucophane and riebeckite has been demonstrated for the conditions prevailing during metamorphism in the Cazadero and New Caledonian blueschists. Linear relationships are found between unit-cell dimensions and variations in composition between glaucophane and riebeckite. The alkali amphiboles of glaucophane compositions belong to the high pressure-low temperature series, glaucophane II-riebeckite. Limited miscibility of actinolite in glaucophane may be characteristic of blueschist facies metamorphism.

California

87Sr/86Sr ratios in some eugeosynclinal sedimentary rocks and their bearing on the origin of granitic magma in orogenic belts

Rb and Sr contents and 87 Sr/ 86 Sr values were determined for samples of eugeosynclinal sedimentary rocks, mostly graywackes, from Oregon and California. These data are compatible with the theory of anataxis of eugeosynclinal sedimentary rocks in orogenic belts to produce granitic magmas provided that the melting occurs within several hundreds of m.y. after sedimentation. The low ( 87 Sr/ 86 Sr) 0 values of the eugeosynclinal sedimentary rocks are related to the significant amounts of volcanogenic detritus present which probably were originally derived from the mantle.

Earth and Planetary Science Letters

Glaucophane schists from California and New Caledonia

In California and New Caledonia, metamorphism of eugeosynclinal rocks has produced blueschist facies in limited areas. The outcrop pattern and structure suggest that the shape of the zone of blueschist metamorphism is elongate parallel to major tectonic trends. Juxtaposition of large ultramafic bodies, subparallel to the blueschist belts, indicates a close tectonic relationship between metamorphism and the tectonic emplacement of the ultramafic masses. Initial emplacement of ultramafics along the depressed axis of the eugeosyncline may have produced deformation related to blueschist metamorphism. Mineral assemblages developed in blueschist facies are characterized by having formed under conditions where pressure is predominant over temperature. That pressure is relatively high requires extremely low thermal gradients combined with a rheology that would allow development of tectonic overpressures.

California

Eclogites and eclogites: Their differences and similarities

Eclogites are divisible into three groups based on mode of occurrence: Group A, inclusions in kimberlites, basalts, or layers in ultramafic rocks; Group B, bands or lenses within migmatite gneissic terrains; Group C, bands or lenses within alpine-type metamorphic rocks. The compositions range from olivine basalt for Group A to tholeiitic basalts for Group C. New analytical data on six eclogites from glaucophane schist terrains in California and New Caledonia now permit comparisons among the three eclogite types. The pyrope content of the garnets is distinctive for each group as follows: Group A, greater than 55 per cent py; Group B, 30–55 per cent py; Group C, less than 30 percent py. Pyroxenes coexisting with these garnets also reflect a compositional change related to their occurrence. The jadeite content progressively increases from Group A through Group B, whereas the diopside content decreases. A comparison of eclogites from different geologic occurrences but with similar bulk compositions demonstrates variation in Ca-Mg partition between coexisting garnet and pyroxene. The Ca/Mg ratio increases in garnet and decreases in pyroxene from Group A through Group B eclogites. This obvious difference in the Ca-Mg partition between coexisting garnet-pyroxene in eclogites of the same bulk composition indicates a broad range of pressure-temperature conditions obtained during crystallization. Experimental synthesis of eclogite-like material at high pressures and temperatures demonstrates that some eclogites may form in the earth's mantle, but naturally occurring Group C eclogites have coexisting garnet-pyroxene with distinct Ca/Mg ratios when compared to Group A or B eclogites of similar bulk composition. This difference in the Ca/Mg ratio must reflect the pressure-temperature conditions characterizing the glaucophane schist facies.

GSA Bulletin