USGS Science⌕ Search

SEARCH · USGS Science

Results for “Chemistry”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,621 records · Page 90Linked to original sources
USGS1991

Weathering processes and the composition of inorganic material transported through the Orinoco River system, Venezuela and Colombia

The composition of river-borne material in the Orinoco River system is related primarily to erosion regime, which in turn is related to tectonic setting; especially notable is the contrast between material derived from tectonically active mountain belts and that from stable cratonic regions. For a particular morpho-tectonic region, the compositional suites of suspended sediment, bed material, overback deposits, and dissolved phases are fairly uniform are are typically distinct from whose of other regions. For each region, a consistent set of chemical weathering reactions can be formulated to explain the composition of dissolved and solid loads. In developing these formulations, erosion on slopes and storage of solids in soils and alluvial sediments are important considerations. Compositionally verymature sediment is derived from areas of thick soils where erosion is transport limited and from areas where sediments are stored for extended periods of time in alluvial deposits. Compositionally immature sediments are derived from tectonically active mountain belts where erosion is weathering limited. Weathering-limited erosion also is important in the elevated parts of the Guayana Shield within areas of sleep topography. Compared to the mountain belts, sediments derived from elevated parts of the Shield are more mature. A greater degree of chemical weathering seems to be needed to erode the rock types typical of the Shield. The major-element chemistry and mineral composition of sediment delivered by the Orinoco River to the ocean are controlled by rivers that have their headwaters in mountain belts and cross the Llanos, a region of alluvial plains within the foreland basin. The composition of sediments in rivers that drain the Shield seems to be established primarily at the site of soil formation, whereas for rivers that drain the mountain belts, additional weathering occurs during s episodes of storage on alluvial plains as sediments are transported across the Llanos to the main stem of the Orinoco. After mixing into the main stem, there seems to be little subsequent alteration of sediment.

Orinoco River↗
USGS1972

Imaging experiment: The Viking Lander

The Viking Lander Imaging System will consist of two identical facsimile cameras. Each camera has a high-resolution mode with an instantaneous field of view of 0.04°, and survey and color modes with instantaneous fields of view of 0.12°. Cameras are positioned one meter apart to provide stereoscopic coverage of the near-field. The Imaging Experiment will provide important information about the morphology, composition, and origin of the Martian surface and atmospheric features. In addition, lander pictures will provide supporting information for other experiments in biology, organic chemistry, meteorology, and physical properties.

Icarus↗
USGS1972

Mass spectrometric analysis of organic compounds, water and volatile constituents in the atmosphere and surface of Mars: The Viking Mars Lander

An experiment centering around a mass spectrometer is described, which is aimed at the identification of organic substances present in the top 10 cm of the surface of Mars and an analysis of the atmosphere for major and minor constituents as well as isotopic abundances. In addition, an indication of the abundance of water in the surface and some information concerning the mineralogy can be obtained by monitoring the gases produced upon heating the soil sample. The organic material will simply be expelled by heating to 150°, 300°, and 500° into the carrier gas stream of a gas chromatograph interfaced to the mass spectrometer or by slowly heating the sample in direct communication with the spectrometer. It is planned to analyze a total of up to nine soil samples in order to study diurnal and seasonal variations. The system is designed to give useful data even for minor constituents if the total of organics should be as low as 5ppm. The spectrometer covers the mass range of 12–200 with adequate resolution. The results of these experiments, which are deliberately designed to cover a wide spectrum of possibilities independent of terrestrial models, are expected to produce a good picture of the planet's organic chemistry and its possible biological significance as well as allow conclusions regarding the history of the planet's atmosphere.

Icarus↗
USGS1988

Experimental studies in stream-aquifer interaction along the Arkansas River in Central Kansas - Field testing and analysis

During the last several years, streamflows of a number of Kansas streams have been reduced as a result of groundwater declines. In order to better understand and quantify stream-aquifer interrelationships, an eight-day comprehensive stream-aquifer pumping test, followed by recovery monitoring, was conducted along the Arkansas River near Great Bend, Kansas. In addition to water level monitoring in numerous observation wells, streamflow data, streambed hydraulic gradients, neutron probe-based water content of dewatered sediments, water chemistry and other data were collected. The alluvial aquifer is shown to be highly transmissive ( T = 1803 m 2 d −1 ) with the pumping stress (9538 m 3 d −1 ) having a radius of influence larger than 1.77 km, impacting both the aquifer levels and the streamflow in the nearby Arkansas River. Drawdown and recharge boundary effects were observed in all observation wells, including those on the opposite side of the river. The alluvial aquifer did not exhibit a water table behavior and responded as a leaky confined aquifer. A semiconfining clay layer less than 3 m thick and an additional recharge source from a nearby stream-alluvial system were the probable causes of the observed phenomena. Actual streamflow depletion is shown to be appreciably less than the computed depletion based on analytical solutions.

Kansas↗
USGS1990

Effect of faults on fluid flow and chloride contamination in a carbonate aquifer system

A unified, multidiscipline hypothesis is proposed to explain the anomalous pattern by which chloride has been found in water of the Upper Floridan aquifer in Brunswick, Glynn County, Georgia. Analyses of geophysical, hydraulic, water chemistry, and aquifer test data using the equivalent porous medium (EPM) approach are used to support the hypothesis and to improve further the understanding of the fracture-flow system in this area. Using the data presented herein we show that: (1) four major northeast-southwest trending faults, capable of affecting the flow system of the Upper Floridan aquifer, can be inferred from structural analysis of geophysical data and from regional fault patterns; (2) the proposed faults account for the anomalous northeastward elongation of the potentiometric surface of the Upper Floridan aquifer; (3) the faults breach the nearly impermeable units that confine the Upper Floridan aquifer from below, allowing substantial quantities of water to leak vertically upward; as a result, aquifer transmissivity need not be excessively large (as previously reported) to sustain the heavy, long-term pumpage at Brunswick without developing a steep cone of depression in the potentiometric surface; (4) increased fracturing at the intersection of the faults enhances the development of conduits that allow the upward migration of high-chloride water in response to pumping from the Upper Floridan aquifer; and (5) the anomalous movement of the chloride plume is almost entirely controlled by the faults.

Georgia↗
USGS1991

Geochemistry of dissolved inorganic carbon in a Coastal Plain aquifer. 1. Sulfate from confining beds as an oxidant in microbial CO2 production

A primary source of dissolved inorganic carbon (DIC) in the Black Creek aquifer of South Carolina is carbon dioxide produced by microbially mediated oxidation of sedimentary organic matter. Groundwater chemistry data indicate, however, that the available mass of inorganic electron acceptors (oxygen, Fe(III), and sulfate) and observed methane production is inadequate to account for observed CO 2 production. Although sulfate concentrations are low (approximately 0.05–0.10 mM) in aquifer water throughout the flow system, sulfate concentrations are greater in confining-bed pore water (0.4–20 mM). The distribution of culturable sulfate-reducing bacteria in these sediments suggests that this concentration gradient is maintained by greater sulfate-reducing activity in sands than in clays. Calculations based on Fick's Law indicate that possible rates of sulfate diffusion to aquifer sediments are sufficient to explain observed rates of CO 2 production (about 10 −5 mmoll −1 year −1 ), thus eliminating the apparent electron-acceptor deficit. Furthermore, concentrations of dissolved hydrogen in aquifer water are in the range characteristic of sulfate reduction (2–6 nM), which provides independent evidence that sulfate reduction is the predominant terminal electron-accepting process in this system. The observed accumulation of pyrite- and calcite-cemented sandstones at sand-clay interfaces is direct physical evidence that these processes have been continuing over the history of these sediments.

Journal of Hydrology↗
USGS1994

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

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.

LITHOS↗
USGS1982

Chemical and isotopic diversity in basalts dredged from the East Pacific Rise at 10°S, the fossil Galapagos Rise and the Nazca plate

We present petrographic, chemical and isotopic data for fresh lava samples dredged from three regions: (1) the fossil Galapagos Rise; (2) an elongate volcano near this extinct spreading center; and (3) the East Pacific Rise at 10°S. The samples from the Galapagos Rise are among the first samples from any fossil spreading center to be analyzed. Alkalic picrites from the elongate seamount and transitional basalts from the East Pacific Rise are both somewhat unusual rock types considering their respective tectonic environments. The dredges from the East Pacific Rise at about 10°S recovered unusual transitional, light rare-earth element (LREE) enriched basalts which show a range of fractionation. On the basis of their chemical and isotopic abundances, it is unlikely that the lavas are related by a single simple process of magmatic differentiation. We suggest that the mantle source region of these basalts was chemically and isotopically heterogeneous. The chemistry of LREE-depleted tholeiitic basalt dredged from near the axis of the extinct Galapagos Rise indicates complex petrogenesis and differentiation. The presence of tholeiitic basalts here indicates that unlike the Guadalupe and Mathematician fossil ridges, the Galapagos Rise has not been the site of voluminous post-abandonment alkalic volcanism. Alkalic basalts of picritic bulk composition dredged from an elongate seamount near the Galapagos Rise do not represent liquid compositions. Instead, we suggest that these alkalic liquids contain added olivine and plagioclase xenocrysts. Although most of the samples analyzed are very fresh, a few have been altered. The latter exhibit characteristic chemical and isotopic effects of seawater alteration.

Marine Geology↗
USGS1995

Fate, bioavailability and toxicity of silver in estuarine environments

The chemistry and bioavailability of Ag contribute to its high toxicity in marine and estuarine waters. Silver is unusual, in that both the dominant speciation reaction in seawater and the processes important in sorbing Ag in sediments favour enhanced bioavailability. Formation of a stable chloro complex favours dispersal of dissolved Ag, and the abundant chloro complex is available to biota. Sequestration by sediments also occurs, but with relatively slow kinetics. Amorphous aggregated coatings enhance Ag accumulation in sediments, as well as Ag uptake from sediments by deposit feeders. In estuaries, the bioaccumulation of Ag increases 56-fold with each unit of increased Ag concentration in sediments. Toxicity for sensitive marine species occurs at absolute concentrations as low as those observed for any nonalkylated metal, partly because bioaccumulation increases so steeply with contamination. The environmental window of tolerance to Ag in estuaries could be narrower than for many elements.

Marine Pollution Bulletin↗
USGS1989

Geochemical and paleoenvironmental variations across the Cretaceous/Tertiary boundary at Braggs, Alabama

The Cretaceous/Tertiary (K/T) boundary in southern Alabama occurs in a sequence of interbedded shallow-marine limestones and marls deposited during a Late Maastrichtian regression and subsequent Danian transgression. The presence of a diverse assemblage of Cretaceous and Paleocene benthic micro- and macrofossils has allowed detailed examination of paleoenvironmental changes in this shallow-marine setting at the time of the K/T boundary extinctions. Although extensive diagenesis has resulted in the recrystallization and cementation of whole rock carbonate, a few molluscan macrofossils have retained their original calcitic structure. The oxygen isotopic record of these macrofossils shows a gradual cooling of 2–3°C over a 3 m.y. period which began in the late Maastrichtian and continued into the Danian. The characteristic depletion in δ 13 C across the K/T boundary displayed by planktonic microfossils from pelagic sequences is not recorded at Braggs. Major changes in whole rock trace and minor element chemistry reflect the decrease in terrigenous mineral fluxes to this location brought about by the rapid Early Paleocene transgression.

Alabama↗
USGS1994

Carbonate deposition, Pyramid Lake subbasin, Nevada: 1. Sequence of formation and elevational distribution of carbonate deposits (Tufas)

During the late Quaternary, the elevation of terrace cutting and carbonate deposition in the Pyramid Lake subbasin were controlled by constancy of lake level imposed by spill to adjoining subbasins. Sill elevations are 1177-1183 m (Mud Lake Slough Sill), 1207 m (Emerson Pass Sill), and 1265 m (Darwin Pass Sill). Carbonate deposition was favored by: (1) hydrologic closure, (2) proximity to a source of calcium, (3) elevated water temperature, and (4) a solid substrate. The thickness and aspect of tufa are a function of lake-level dynamics. Relatively thin sheets and pendant sheets were deposited during a rising or falling lake. The upper parts of thick reef-form tufas have a horizontal aspect and were deposited in a lake which was stabilized by spill to the Carson Desert subbasin. The lower parts of the reef-form tufas are thinner and their outer surface has a vertical aspect, indicating that the lower part formed in a receding lake. The thickest and most complete sequences of tufa are mounds that border the Pyramid Lake shore. The tops of the tallest mounds reach the elevation of the Darwin Pass Sill and many mounds have been eroded to the elevations of the Mud Lake Slough Sill of the Emerson Pass Sill. The sequence of tufa formation (from oldest to youngest) displayed in these mounds is: (1) a beachrock containing carbonate-cemented volcanic cobbles, (2) broken and eroded old spheroids that contain thinolitic tufa and an outer rind of dense laminated tufa, (3) large cylindrical (tubular) tufas capped by (4) coatings of old dense tufas, and (5) several generations of old branching tufa commonly associated with thin, platy tufas and coatings of thinolitic tufa, (6) young spheroids that contain poorly oriented young thinolitic tufa in the center and several generations of radially oriented young thinolitic tufas near the outer edge, (7) a transitional thinolite-to-branching tufa, (8) two or more layers of young branching tufa, (9) a 0.5-cm-thick layer of fine-grained dolomite, (10) a 2-cm-thick layer of young dense laminated tufa, (11) a 0.1-cm-thick layer of encrusting tufa that was covered by a beach deposit and (12) a 1.0-cm-thick layer of porous encrusting tufa that coated the beach deposit and the sides of tufa mounds. The elevational ranges of the principal varieties of tufa are not related to terrace or spill elevations. It seems likely that the distribution of tufa varieties is related to variation in the thermal structure or chemistry of Lake Lahontan. It is hypothesized that the thinolitic tufa (ikaite) formed in the near freezing hypolimnion and the braching tufa (calcite) formed in the seasonally warmer epiliminion of the lake.

Nevada↗
USGS1989

The influence of reagent type on the kinetics of ultrafine coal flotation

A kinetic study has been conducted to determine the influence of reagent type on flotation rates of ultrafine coal. Two ultrafine coal samples, the Illinois No. 5 (Springfield) and Pittsburgh No. 8, have been evaluated with various reagent types in order to derive the rate constants for coal (k c ), ash (k a ), and pyrite (k c ). The reagents used in the study include anionic surfactants, anionic surfactant—alcohol mixtures, and frothing alcohols. In general, the surfactant-alcohol mixtures tend to float ultrafine coal at a rate three to four times faster than either pure alcohols or pure anionic surfactants. Pine oil, a mixture of terpene alcohols and hydrocarbons, was an exception to this finding; it exhibited higher rate constants than the pure aliphatic alcohols or other pure anionic surfactants studied; this may be explained by the fact that the sample of pine oil used (70% alpha-terpineol) acted as a frother/collector system similar to alcohol/kerosene. The separation efficiencies of ash and pyrite from coal, as evidenced by the ratios of k c /k a or k c /k p , tend to indicate, however, that commercially available surfactant—alcohol mixtures are not as selective as pure alcohols such as 2-ethyl-1-hexanol or methylisobutylcarbinol. Some distinct differences in various rate constants, or their ratios, were noted between the two coals studied, and are possibly attributable to surface chemistry effects.

Powder Technology↗
USGS2017

Isotopic evidence for glacial meltwater recharge to the Cambrian-Ordovician aquifer, north-central United States

The chemistry of water in the Cambrian-Ordovician aquifer in six midwestern states has been studied as part of the Northern Midwest Regional Aquifer-System Analysis of the U.S. Geological Survey. Dissolved-solids concentrations generally increase perpendicular to the direction of regional groundwater flow, from less than 400 mg/liter in southeast Minnesota, southwest Wisconsin, and northeast Iowa to more than 10,000 mg/liter in northwest Missouri. Isotopic ratios of hydrogen and oxygen are significantly depleted from north to south, with an areal distribution approximately parallel to the distribution of dissolved solids. For example, ??18O in southern Iowa and northern Missouri is about 6 parts per thousand lighter than ??18O of modern recharge water in Minnesota and Wisconsin. Covariance between ??18O and ??D of the groundwater, similar to that of modern precipitation, suggests that the differences in isotopic ratios between groundwater and modern recharge water reflect meteoric signatures of water during past recharge events rather than geochemical processes such as isotopic exchange with aquifer materials. The pronounced parallelism between the distribution of isotopes and dissolved solids over large areas probably reflects largescale recharge of Pleistocene glacial meltwater into the aquifer system, which probably had a paleoflow system with a gradient from northeast to southwest rather than from northwest to southeast. ?? 1984.

Quaternary Research↗
USGS1993

Mapping playa evaporite minerals with AVIRIS data: A first report from Death Valley, California

Efflorescent salt crusts in Death Valley, California, were mapped by using Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data and a recently developed least-squares spectral band-fitting algorithm. Eight different saline minerals were remotely identified, including three borates, hydroboracite, pinnoite, and rivadavite, that have not been previously reported from the Death Valley efflorescent crusts. The three borates are locally important phases in the crusts, and at least one of the minerals, rivadavite, appears to be forming directly from brine. Borates and other evaporite minerals provide a basis for making remote chemical measurements of desert hydrologic systems. For example, in the Eagle Borax Spring area, the AVIRIS mineral maps pointed to elevated magnesium and boron levels in the ground waters, and to the action of chemical divides causing subsurface fractionation of calcium. Many other chemical aspects of playa brines should have an expression in the associated evaporite assemblages. Certain anhydrous evaporites, including anhydrite, glauberite, and thenardite, lack absorption bands in the visible and near-infrared wavelength range, and crusts composed of these minerals could not be characterized by using AVIRIS. In these situations, thermal-infrared remote sensing data may complement visible and near-infrared data for mapping evaporites. Another problem occurred in wet areas of Death Valley, where water absorption caused low signal levels in the 2.0-2.5 ??m wavelength region that obscured any spectral features of evaporite minerals. Despite these difficulties, the results of this study demonstrate the potential for using AVIRIS and other imaging spectrometer data to study playa chemistry. Such data can be useful for understanding chemical linkages between evaporites and ground waters, and will facilitate studies of how desert ground-water regimes change through time in response to climatic and other variables.

California↗
USGS1989

Geochemistry and diagenesis of Miocene lacustrine siliceous sedimentary and pyroclastic rocks, Mytilinii basin, Samos Island, Greece

A Late Miocene non-marine stratigraphic sequence composed of limestone, opal-CT-bearing limestone, porcelanite, marlstone, diatomaceous marlstone, dolomite, and tuffite crops out on eastern Samos Island. This lacustrine sequence is subdivided into the Hora Beds and the underlying Pythagorion Formation. The Hora Beds is overlain by the clastic Mytilinii series which contains Turolian (Late Miocene) mammalian fossils. The lacustrine sequence contains volcanic glass and the silica polymorphs opal-A, opal-CT, and quartz. Volcanic glass predominantly occurs in tuffaceous rocks from the lower and upper parts of the lacustrine sequence. Opal-A (diatom frustules) is confined to layers in the upper part of the Hora Beds. Beds rich in opal-CT underlie those containing opal-A. The occurrence of opal-CT is extensive, encompassing the lower Hora Beds and the sedimentary rocks and tuffs of the Pythagorion Formation. A transition zone between the opal-A and opal-CT zones is identified by X-ray diffraction patterns that are intermediate between those of opal-CT and opal-A, perhaps due to a mixture of the two polymorphs. Diagenesis was not advanced enough for opal-CT to transform to quartz or for volcanic glass to transform to opal-C. Based on geochemical and mineralogical data, we suggest that the rate of diagenetic transformation of opal-A to opal-CT was mainly controlled by the chemistry of pore fluids. Pore fluids were characterized by high salinity, moderately high alkalinity, and high magnesium ion activity. These pore fluid characteristics are indicated by the presence of evaporitic salts (halite, sylvite, niter), high boron content in biogenic silica, and by dolomite in both the opal-A and opal-CT-bearing beds. The absence of authigenic K-feldspar, borosilicates, and zeolites also support these pore fluid characteristics. Additional factors that influenced the rate of silica diagenesis were host rock lithology and the relatively high heat flow in the Aegean region from Miocene to Holocene.

Samos Island↗
USGS1989

Geology of the Zambales ophiolite, Luzon, Philippines

The Zambales ophiolite of western Luzon, Philippines, exposes a typical succession of basalt flows, diabasic dikes, gabbro and tectonized harzburgite. The age established by limiting strata is late Eocene. Lack of evidence of thrust faulting and the general domal disposition of the lithologie units indicate that the ophiolitic rocks are exposed by uplift. Highly complex internal layered structures within the complex are related to processes developed during formation of the ophiolite and the Zambales ophiolite may be one of the least disturbed (by emplacement) ophiolitic masses known. The exposed mass trends north and the upper surface plunges at low angles (a few degrees) to the north and south. The chemistry and composition of the rocks in the northwest part of the Zambales area (Acoje block) is distinct from that in the southeastern segment (Coto block). The Acoje block, according to Evans (1983) and Hawkins and Evans (1983), resembles (on a chemical basis) arc-tholeiite series rocks from intra-island arcs and the rocks in the Coto block are typical back-arc basin rock series. The present writer believes that the ophiolite composes a single genetic unit and that the changes in composition are the result of changes that took place during the initial formation. The gabbro probably formed below a spreading center in an elongate, in cross section, V-shaped, magma chamber. The gabbro is estimated by the writer to be less than 2 km thick and may be less than 1 km in places. Numerous erosional windows through the gabbro in the northern and eastern side of the Zambales area show that the gabbro remaining in those areas is likely to be only a few hundred meters thick. Harzburgite is exposed to a depth of about 800 m in the Bagsit River area and this may be the deepest part of the ophiolite accessible for study on which there is any control on depth. A transitional zone, about 200 m thick lying between the gabbro and harzburgite, is composed of serpentinized dunite. Commonly the dunite contains disseminated sulfide minerals and at the Acoje Mines, platinum-group elements. A compositional layering within the gabbro is in places cumulate in the lower part of the unit but may have formed by nucleation higher up on the relatively steep sides of the magma chamber. A widespread gneissic banding in the gabbro forms large mappable structures which are many times more complex than is the disposition of the major rock units. These structures are believed to be the result of extensive slumping in the magma chamber. The structure produced by the cumulate layering merges with the gneissic banding, commonly without discernible change in attitude. This tectonic layered structure crosses the gabbro-peridotite boundary at any angle without seeming to disturb the original rock distribution. At greater depths below the boundary (ca. 800 m), the harzburgite contains low dipping banding, which probably reflects the result of differential movement within the mantle. Chromite occurs almost exclusively in a zone that generally lies no more than 200–300 m below the gabbro-peridotite boundary. Refractory-grade chromite is found in this zone below the olivine gabbro in the Goto block and as low-grade metallurgical grade chromite below norite in the Acoje block. At Acoje Mines the chromite is present in layers in dunite, which the writer interprets as being distributed in a zone along the gently dipping (ca. 25°) gabbro-peridotite boundary. The steeply dipping (ca. 60–80 ° ) individual layers lie en echelon along the boundary at an angle (ca. 50 ° ) to the contact. At Coto the chromite forms large discontinuous masses in the lowest dunite and in the uppermost harzburgite. Except for the chromite present as layers at Acoje, the regional tectonic layering crosses the chromite deposits without structural deviation. The chromite deposits and associated peridotite may be cumulate in origin, but have been modified to such an extent that cumulate textures are generally obliterated. The angle of repose of cumulate layers in the Acoje area and in the Coto block dip towards each other raising the possibility that the Zambales area may contain the relics of a spreading center. Initial emplacement of the Zambales ophiolite took place by uplift and the ultramafic portion was exposed to erosion in the earliest Miocene or late Oligocene. Submergence of some of the ophiolite followed the previous uplift and on the west side of the Zambales Range submergence of several kilometers is indicated. Final emergence appears to have taken place in Pliocene or Pleistocene time by block uplift and areas of greatest uplift closely conform to the present topographic surface.

Tectonophysics↗
USGS1992

A-type granite and the Red Sea opening

Miocene-Oligocene A-type granite intrudes the eastern side of the Red Sea margin within the zone of extension from Jiddah, Saudi Arabia south to Yemen. The intrusions developed in the early stages of continental extension as Arabia began to move slowly away from Africa (around 30–20 Ma). Within the narrow zone of extension silicic magmas formed dikes, sills, small plutons and extrusive equivalents. In the Jabal Tirf area of Saudi Arabia these rocks occur in an elongate zone consisting of late Precambrian basement to the east, which is gradually invaded by mafic dikes. The number of dikes increases westward until an igneous complex is produced parallel to the present Red Sea axis. The Jabal Tirf igneous complex consists of diabase and rhyolite-granophyre sills (20–24 Ma). Although these are intrusine intrusive rocks their textures indicate shallow depths of intrusion (< 1 km). To the south, in the Yemen, contemporaneous with alkali basaltic eruptions (26–30 Ma) and later silicic eruptions, small plutons, dikes, and stocks of alkali granite invaded thick (1500 m) volcanic series, at various levels and times. Erosion within the uplifted margin of Yemen suggests that the maximum depth of intrusion was less than 1–2 km. Granophyric intrusions (20–30 Ma) within mafic dike swarms similar to the Jabal Tirf complex are present along the western edge of the Yemen volcanic plateau, marking a north-south zone of continental extension. The alkali granites of Yemen consist primarily of perthitic feldspar and quartz with some minor alkali amphiboles and acmite. These granites represent water-poor, hypersolvus magmas generated from parent alkali basalt magmas. The granophyric, two-feldspar granites associated with the mafic dike swarms and layered gabbros formed by fractional crystallization from tholeiitic basalt parent developed in the early stages of extension. Initial 87 Sr/ 86 Sr ratios of these rocks and their bulk chemistry indicate that production of peralkaline and metaluminous granitic magmas involved both fractiónation and partial melting as they ascended through the late Precambrian crust of the Arabian plate.

Red Sea↗
USGS1982

Characterization of dissolved organic materials in surface waters within the blast zone of Mount St Helens, Washington

After the May 18, 1980, eruption of Mount St Helens, the concentration of dissolved organic material in surface waters near the volcano increased significantly as a result of the destruction of the surrounding conifer forest. Low molecular weight organic compounds identified in the blast zone surface waters were derived from pyrolysis of plant and soil organic materials incorporated into pyroclastic flow, mud flow and debris avalanche deposits. A major fraction of the dissolved organic material consisted of high molecular weight, colored, organic acids that are similar in their general properties to aquatic fulvic acids found in more typical surface waters except for greater sulfur contents. The other major fraction of the dissolved organic material consisted of hydrophilic acids, which may include compounds capable of supporting heterotrophic microorganisms, and precursors in the formation of aquatic fulvic acids. The organic chemistry of blast zone surface waters will probably be greatly influenced by the May 18, 1980, eruption for many years.

Washington↗