Geology topics

R.A. Zierenberg

Publications and source records attributed to R.A. Zierenberg.

6 recordsLinked to original sources

USGS2012

Composition and origin of rhyolite melt intersected by drilling in the Krafla geothermal field, Iceland

The Iceland Deep Drilling Project Well 1 was designed as a 4- to 5-km-deep exploration well with the goal of intercepting supercritical hydrothermal fluids in the Krafla geothermal field, Iceland. The well unexpectedly drilled into a high-silica (76.5 % SiO 2 ) rhyolite melt at approximately 2.1 km. Some of the melt vesiculated while extruding into the drill hole, but most of the recovered cuttings are quenched sparsely phyric, vesicle-poor glass. The phenocryst assemblage is comprised of titanomagnetite, plagioclase, augite, and pigeonite. Compositional zoning in plagioclase and exsolution lamellae in augite and pigeonite record changing crystallization conditions as the melt migrated to its present depth of emplacement. The in situ temperature of the melt is estimated to be between 850 and 920 °C based on two-pyroxene geothermometry and modeling of the crystallization sequence. Volatile content of the glass indicated partial degassing at an in situ pressure that is above hydrostatic (~16 MPa) and below lithostatic (~55 MPa). The major element and minor element composition of the melt are consistent with an origin by partial melting of hydrothermally altered basaltic crust at depth, similar to rhyolite erupted within the Krafla Caldera. Chondrite-normalized REE concentrations show strong light REE enrichment and relative flat patterns with negative Eu anomaly. Strontium isotope values (0.70328) are consistent with mantle-derived melt, but oxygen and hydrogen isotope values are depleted (3.1 and −118 ‰, respectively) relative to mantle values. The hydrogen isotope values overlap those of hydrothermal epidote from rocks altered by the meteoric-water-recharged Krafla geothermal system. The rhyolite melt was emplaced into and has reacted with a felsic intrusive suite that has nearly identical composition. The felsite is composed of quartz, alkali feldspar, plagioclase, titanomagnetite, and augite. Emplacement of the rhyolite magma has resulted in partial melting of the felsite, accompanied locally by partial assimilation. The interstitial melt in the felsite has similar normalized SiO 2 content as the rhyolite melt but is distinguished by higher K 2 O and lower CaO and plots near the minimum melt composition in the granite system. Augite in the partially melted felsite has re-equilibrated to more calcic metamorphic compositions. Rare quenched glass fragments containing glomeroporphyritic crystals derived from the felsite show textural evidence for resorption of alkali feldspar and quartz. The glass in these fragments is enriched in SiO 2 relative to the rhyolite melt or the interstitial felsite melt, consistent with the textural evidence for quartz dissolution. The quenching of these melts by drilling fluids at in situ conditions preserves details of the melt–wall rock interaction that would not be readily observed in rocks that had completely crystallized. However, these processes may be recognizable by a combination of textural analysis and in situ analytical techniques that document compositional heterogeneity due to partial melting and local assimilation.

Contributions to Mineralogy and Petrology↗

USGS2012

Mineralization, alteration, and hydrothermal metamorphism of the ophiolite-hosted Turner-Albright sulfide deposit, southwestern Oregon

The Turner-Albright sulfide deposit, part of the Josephine ophiolite, formed on and below the seafloor during Late Jurassic volcanism at a back arc spreading center. Ore fluids were probably localized by faults which were active on the seafloor at the time of sulfide deposition. The uppermost massive sulfide formed on the seafloor at hydrothermal vents, similar to sulfide-depositing hot springs on modern spreading centers. The bulk of the sulfide mineralization formed below the seafloor within olivine basalt hyaloclastite erupted near the time of mineralization. Infiltration of hydrothermal fluid into the hyalo-clastite altered the rock to quartz + Fe-chlorite and quartz + sericite + Fe-chlorite. Intense alteration resulted in replacement of the protolith by quartz + sulfide. The fluid responsible for the hydrothermal alteration was evolved seawater with low p H and Mg and high Fe. Sulfide δ 534 S values average 4.7‰ and indicate contribution of sulfur from both basalt and seawater sulfate. The average value of sulfide δ 34 S and the difference between sulfide and contemporaneous seawater sulfate δ 34 S values are similar to ophiolite-hosted sulfide deposits in Cyprus. Chlorite-rich hydrothermally altered basalt has δ 18 O values of 3.0–6.8‰ due to high-temperature (250°–350°C) reaction with a seawater-derived ore fluid. Quartz in silicified basalt has higher δ 18 O values of 12.3–15.5‰, probably reflecting lower-temperature recrystallization of amorphous silica formed during initial alteration of basalt. Mudstone and clinopyroxene basalt above the sulfide horizons were not altered by the ore-transporting hydrothermal fluid, but these rocks were hydrothermally metamorphosed by altered seawater heated by deep circulation into hot oceanic crust. This subseafloor metamorphism produced a mineral assemblage typical of prehnite-pumpellyite facies metamorphism. Exchange with altered seawater increased the whole-rock δ 18 O of the basalts to values of 9.4–11.2‰.

Journal of Geophysical Research Solid Earth↗

USGS2011

Origin of a rhyolite that intruded a geothermal well while drilling at the Krafla volcano, Iceland

Magma flowed into an exploratory geothermal well at 2.1 km depth being drilled in the Krafla central volcano in Iceland, creating a unique opportunity to study rhyolite magma in situ in a basaltic environment. The quenched magma is a partly vesicular, sparsely phyric, glass containing ∼1.8% of dissolved volatiles. Based on calculated H 2 O-CO 2 saturation pressures, it degassed at a pressure intermediate between hydrostatic and lithostatic, and geothermometry indicates that the crystals in the melt formed at ∼900 °C. The glass shows no signs of hydrothermal alteration, but its hydrogen and oxygen isotopic ratios are much lower than those of typical mantle-derived magmas, indicating that this rhyolite originated by anhydrous mantle-derived magma assimilating partially melted hydrothermally altered basalts.

Krafla volcano↗

USGS1998

The deep structure of a sea-floor hydrothermal deposit

Hydrothermal circulation at the crests of mid-ocean ridges plays an important role in transferring heat from the interior of the Earth. A consequence of this hydrothermal circulation is the formation of metallic ore bodies known as volcanic-associated massive sulphide deposits. Such deposits, preserved on land, were important sources of copper for ancient civilizations and continue to provide a significant source of base metals (for example, copper and zinc). Here we present results from Ocean Drilling Program Leg 169, which drilled through a massive sulphide deposit on the northern Juan de Fuca spreading centre and penetrated the hydrothermal feeder zone through which the metal-rich fluids reached the sea floor. We found that the style of feeder-zone mineralization changes with depth in response to changes in the pore pressure of the hydrothermal fluids and discovered a stratified zone of high-grade copper-rich replacement mineralization below the massive sulphide deposit. This copper-rich zone represents a type of mineralization not previously observed below sea-floor deposits, and may provide new targets for land-based mineral exploration.

Nature↗

USGS1995

Alteration of basalt hyaloclastite at the off-axis Sea Cliff hydrothermal field, Gorda Ridge

The Sea Cliff hydrothermal field on the northern segment of the Gorda Ridge is situated along a rift-bounding normal fault about 2.6 km east of the neovolcanic zone and approximately 300 m above the spreading axis. The structural setting of this hydrothermal field differs from that of most other active seafloor hydrothermal sites investigated to date, which are typically situated in the neovolcanic zone. Mineralization occurs in basaltic talus covering a large normal-fault scarp. Hydrothermal crusts cover much of the seafloor in the area of the active hydrothermal field. These crusts form by extensive alteration of basaltic hyaloclastite in a zone of mixing between ascending hydrothermal fluid and entrained seawater. The initial stage of alteration is magnesian metasomatism of both crystalline basalt and basaltic glass, converting the rock to Mg-rich smectite and smectite/chlorite. Further alteration removes nearly all cations and ultimately leads to silicification. Preservation of basaltic texture in the silicified rocks provides evidence that even such sparingly soluble elements as A1 and Ti have been removed. Oxygen-isotopic ratios of the altered rocks constrain initial alteration to temperatures near 220°C, close to the maximum measured vent temperatures of 247°C. Silicification proceeded to much lower temperatures, and most amorphous silica deposition occurred at temperatures below 100°C. Sulfur-, strontium-, and lead-isotopic data all indicate a predominantly basaltic source, with important contributions from seawater but no significant contribution from sedimentary sources. Comparison with ophiolite-hosted massive sulfide deposits shows that the structural setting, alteration sequence, and depositional environment are all similar and suggests that mineralization and replacement of basaltic breccia in the Sea Cliff hydrothermal field likely occur in the subsurface beneath a capping layer of silicified hyaloclastite.

California, Oregon↗

USGS1990

Microbial control of silver mineralization at a sea-floor hydrothermal site on the northern Gorda Ridge

THE Sea Cliff hydrothermal field, on the northern Gorda Ridge, contains mounds and chimneys of hydrothermally precipitated sulphide and sulphate minerals typical of sea-floor hydrothermal vent sites 1 . In addition, large areas of the sea floor are covered by subhorizontal hydrothermal crusts. Samples of the crust recovered by submersible are composed of intensely altered fragments of basalt and basaltic hyaloclastite cemented by amorphous silica and chalcedony with less abundant barite, and minor amounts of base-metal sulphide minerals 2 . Some surfaces of the crust were formerly colonized by bacterial mats, which are locally preserved by replacement and overgrowth of the bacterial filaments by metal sulphide minerals and amorphous silica. The bacterial filaments are selectively replaced by prousite (Ag 3 AsS 3 ), pearceite 3 (Ag 14.7–x Cu 1.3+x As 2 S 11 ), chalcopyrite (CuFeS 2 ) and rarely by galena (PbS). Our observations suggest that bacterially mediated processes selectively precipitate silver, arsenic and copper, and that biological processes may contribute to precious-metal enrichment in some sea-floor hydrothermal base-metal sulphide deposits.

California, Oregon↗