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Randolph A. Koski

Publications and source records attributed to Randolph A. Koski.

At least 19 recordsLinked to original sources
USGS2014

Layered hydrothermal barite-sulfide mound field, East Diamante Caldera, Mariana volcanic arc

East Diamante is a submarine volcano in the southern Mariana arc that is host to a complex caldera ~5 × 10 km (elongated ENE-WSW) that is breached along its northern and southwestern sectors. A large field of barite-sulfide mounds was discovered in June 2009 and revisited in July 2010 with the R/V Natsushima , using the ROV Hyper-Dolphin . The mound field occurs on the northeast flank of a cluster of resurgent dacite domes in the central caldera, near an active black smoker vent field. A 40 Ar/ 39 Ar age of 20,000 ± 4000 years was obtained from a dacite sample. The mound field is aligned along a series of fractures and extends for more than 180 m east-west and >120 m north-south. Individual mounds are typically 1 to 3 m tall and 0.5 to 2 m wide, with lengths from about 3 to 8 m. The mounds are dominated by barite + sphalerite layers with the margins of each layer composed of barite with disseminated sulfides. Rare, inactive spires and chimneys sit atop some mounds and also occur as clusters away from the mounds. Iron and Mn oxides are currently forming small (<1-m diam, ~0.5-m tall) knolls on the top surface of some of the barite-sulfide mounds and may also drape their flanks. Both diffusely and focused fluids emanate from the small oxide knolls. Radiometric ages of the layered barite-sulfide mounds and chimneys vary from ~3,920 to 3,350 years. One layer, from an outcrop of 10- to 100-cm-thick Cu-rich layers, is notably younger with an age of 2,180 years. The Fe-Mn oxides were <5 years old at the time of collection in 2009. Most mound, chimney, and layered outcrop samples are dominated by barite, silica, and sphalerite; other sulfides, in decreasing order of abundance, are galena, chalcopyrite, and rare pyrite. Anglesite, cerussite, and unidentified Pb oxychloride and Pb phosphate minerals occur as late-stage interstitial phases. The samples contain high Zn (up to 23 wt %), Pb (to 16 wt %), Ag (to 487 ppm), and Au (to 19 ppm) contents. Some layered outcrop samples are dominated by chalcopyrite resulting in ≤4.78 wt % Cu in a bulk sample (28 wt % for a single lens), with a mean of 0.28 wt % for other samples. Other significant metal enrichments are Sb (to 1,320 ppm), Cd (to 1,150 ppm), and Hg (to 55 ppm). The East Diamante mound field has a unique set of characteristics compared to other hydrothermal sites in the Mariana arc and elsewhere. The geochemical differences may predominantly reflect the distribution of fractures and faults and consequently the rock/water ratio, temperature of the fluid in the upper parts of the circulation system, and extensive and prolonged mixing with seawater. The location of mineralization is controlled by fractures. Following resurgent doming within the caldera, mineralization resulted from focused flow along small segments of linear fractures rather than from a point source, typical of hydrothermal chimney fields. Based on the mineral assemblage, the maximum fluid temperatures were ~260°C, near the boiling point for the water depths of the mound field (367–406 m). Lateral fluid flow within the mounds precipitated interstitial sphalerite, silica, and Pb minerals within a network of barite with disseminated sulfides; silica was the final phase to precipitate. The current low-temperature precipitation of Fe and Mn oxides and silica may represent rejuvenation of the system.

Economic Geology↗
USGS2012

Volcanism and massive sulfide formation at a sedimented spreading center, Escanaba Trough, Gorda Ridge, northeast Pacific Ocean

Seismic‐reflection profiles over the sediment‐filled Escanaba Trough at the southern Gorda Ridge reveal a series of volcanic centers that pierce the sediment. The volcanic edifices are 3 to 6 km in diameter and are spaced at 15 to 20 km intervals along the axis of the trough. The volcanic intrusions have uplifted the sediment as much as 100 m, and in places fresh basaltic flows are exposed at the sea floor. Unoxidized pyrrhotite‐rich massive‐sulfide samples were obtained from the flanks of one of these volcanic centers. The composition and form of the sulfide samples suggest significant interaction between hydrothermal fluids and sediment at depth, and deposition of sulfide within the sediment pile.

Geophysical Research Letters↗
USGS2012

Compositions, growth mechanisms, and temporal relations of hydrothermal sulfide‐sulfate‐silica chimneys at the northern Cleft segment, Juan de Fuca Ridge

Three active hydrothermal vents forming sulfide mounds and chimneys (Monolith, Fountain, and Pipe Organ) and more widely distributed inactive chimneys are spatially related to a system of discontinuous fissures and young sheet flow lavas at the northern Cleft segment, Juan de Fuca Ridge. The formation of zoned tubular Curich chimneys (type I) on the Monolith sulfide mound is related to focused flow of high‐temperature (to 328°C) fluid. Bulbous chimneys (type II or “beehives”) at the Monolith and Fountain vents are products of diffuse high‐temperature (to 315°C) discharge. A broader zone of vigorous mixing between the hydrothermal fluid and seawater results in quench crystallization of anhydrite‐rich shells. Columnar Zn‐sulfide‐rich chimneys with narrow channelways (type III) are constructed where focused and relatively low‐temperature (261°C) fluid vents directly from the basalt substrate. The bulk chemistry (low Cu; high Pb, Ag, and SiO 2 contents), mineralogy (pyrite‐marcasite‐wurtzite‐amorphous silica‐anglesite), colloform and filamentous textures, and oxygen isotope characteristics of inactive (type IV) chimneys indicate a low‐temperature (<250°C) origin involving diffuse and sluggish flow patterns and conductive cooling. Seafloor observations and 210 Pb data indicate that (1) type IV chimneys are products of an earlier period of hydrothermal activity that ended no more than 60 years ago but prior to the sheet flow eruption, (2) the high‐temperature Monolith and Fountain vents are manifestations of the same heating event (shallow emplacement of magma) that led to the sheet flow eruption and recent megaplumes, and (3) the Pipe Organ Vent is in a very youthful stage of development and chimney deposition postdates the sheet flow eruption.

California, Oregon, Washington↗
USGS2012

Mineralogy and geochemistry of a sediment‐hosted hydrothermal sulfide deposit from the Southern Trough of Guaymas Basin, Gulf of California

Samples dredged from a 15‐m‐high hydrothermal mound atop the flat turbidite pond in the Southern Trough of Guaymas Basin consist of pyrrhotite‐rich massive sulfide, barite, barite + calcite, talc, and opaline silica as well as substrate material composed of fossiliferous, clay‐rich ooze. An 11‐m‐long sediment core taken near the dredge site shows increasing hydrothermal alteration with depth; anhydrite‐filled fractures near the base of the core appear to be channels for hydrothermal discharge. Oxidation of the sulfide‐rich samples to an assemblage of geothite, lepidocrocite, and amorphous Fe oxyhydroxide is ubiquitous. Compared to other massive sulfide deposits on sediment‐starved oceanic ridges, the hydrothermal deposit dredged in Guaymas Basin has a high pyrrhotite/pyrite ratio, a low Zn sulfide and combined ore metal (Cu + Zn + Pb + Ag + Cd) content, and a greater abundance of sulfate, carbonate, and silicate phases. Venting hydrothermal solutions are alkaline with moderately high p H; high Ca, Ba, and SiO 2 content; low ƒS 2 and ƒo 2 ; and very low transition metal content. Disequilibrium assemblages of pyrrhotite and sulfate minerals form during rapid mixing of this evolved vent fluid with ambient bottom waters at the discharge site. Talc is formed at a temperature near 270°C by mixing or entrainment of Mg‐rich bottom water or pore fluid with upwelling hydrothermal fluid that is saturated with silica. Calcite may precipitate from the alkaline, Ca‐rich fluid during degassing of CO 2 . The minimum temperature range for sulfide and nonsulfide deposition is approximately 190°–326°C. The composition of hydrothermal deposits, vent solutions, and altered sediment requires that circulating fluids evolve during deep penetration into the basaltic basement complex, further interaction with the organic‐and carbonate‐rich sediment pile, and near‐surface mixing with ambient seawater. Although the stable assemblage albite‐epidote‐clinochlore present at depth in the sediment pile requires very low dissolved Mg and Fe in the altering fluid, the addition of Mg to deeply buried sediment indicates significant recharge of the system by Guaymas Basin bottom water.

Southern Trough of Guaymas Basin↗
USGS2012

Volcanogenic massive sulfide occurrence model

Volcanogenic massive sulfide deposits, also known as volcanic-hosted massive sulfide, volcanic-associated massive sulfide, or seafloor massive sulfide deposits, are important sources of copper, zinc, lead, gold, and silver (Cu, Zn, Pb, Au, and Ag). These deposits form at or near the seafloor where circulating hydrothermal fluids driven by magmatic heat are quenched through mixing with bottom waters or porewaters in near-seafloor lithologies. Massive sulfide lenses vary widely in shape and size and may be podlike or sheetlike. They are generally stratiform and may occur as multiple lenses. Volcanogenic massive sulfide deposits range in size from small pods of less than a ton (which are commonly scattered through prospective terrains) to supergiant accumulations like Rio Tinto (Spain), 1.5 billion metric tons; Kholodrina (Russia), 300 million metric tons; Windy Craggy (Canada), 300 million metric tons; Brunswick No. 12 (Canada), 230 million metric tons; and Ducktown (United States), 163 million metric tons. Volcanogenic massive sulfide deposits range in age from 3.55 billion years to zero-age deposits that are actively forming in extensional settings on the seafloor, especially mid-ocean ridges, island arcs, and back-arc spreading basins. The widespread recognition of modern seafloor Volcanogenic massive sulfide deposits and associated hydrothermal vent fluids and vent fauna has been one of the most astonishing discoveries in the last 50 years, and seafloor exploration and scientific studies have contributed much to our understanding of ore-forming processes and the tectonic framework for volcanogenic massive sulfide deposits in the marine environment. Massive ore in volcanogenic massive sulfide deposits consists of greater than 40 percent sulfides, usually pyrite, pyrrhotite, chalcopyrite, sphalerite, and galena; non-sulfide gangue typically consists of quartz, barite, anhydrite, iron oxides, chlorite, sericite, talc, and their metamorphosed equivalents. Ore composition may be Pb-Zn-, Cu-Zn-, or Pb-Cu-Zn-dominated, and some deposits are zoned vertically and laterally. Many deposits have stringer or feeder zones beneath the massive zone that consist of crosscutting veins and veinlets of sulfides in a matrix of pervasively altered host rock and gangue. Alteration zonation in the host rocks surrounding the deposits are usually well-developed and include advanced argillic (kaolinite, alunite), argillic (illite, sericite), sericitic (sericite, quartz), chloritic (chlorite, quartz), and propylitic (carbonate, epidote, chlorite) types. An unusual feature of VMS deposits is the common association of stratiform "exhalative" deposits precipitated from hydrothermal fluids emanating into bottom waters. These deposits may extend well beyond the margins of massive sulfide and are typically composed of silica, iron, and manganese oxides, carbonates, sulfates, sulfides, and tourmaline.

Scientific Investigations Report↗
USGS2012

Metal dispersion resulting from mining activities in coastal environments: A pathways approach

Acid rock drainage (ARD) and disposal of tailings that result from mining activities impact coastal areas in many countries. The dispersion of metals from mine sites that are both proximal and distal to the shoreline can be examined using a pathways approach in which physical and chemical processes guide metal transport in the continuum from sources (sulfide minerals) to bioreceptors (marine biota). Large amounts of metals can be physically transported to the coastal environment by intentional or accidental release of sulfide-bearing mine tailings. Oxidation of sulfide minerals results in elevated dissolved metal concentrations in surface waters on land (producing ARD) and in pore waters of submarine tailings. Changes in pH, adsorption by insoluble secondary minerals (e.g., Fe oxyhydroxides), and precipitation of soluble salts (e.g., sulfates) affect dissolved metal fluxes. Evidence for bioaccumulation includes anomalous metal concentrations in bivalves and reef corals, and overlapping Pb isotope ratios for sulfides, shellfish, and seaweed in contaminated environments. Although bioavailability and potential toxicity are, to a large extent, functions of metal speciation, specific uptake pathways, such as adsorption from solution and ingestion of particles, also play important roles. Recent emphasis on broader ecological impacts has led to complementary methodologies involving laboratory toxicity tests and field studies of species richness and diversity.

Oceanography↗
USGS2008

Chemical data for precipitate samples

During studies of sulfide oxidation in coastal areas of Prince William Sound in 2005, precipitate samples were collected from onshore and intertidal locations near the Ellamar, Threeman, and Beatson mine sites (chapter A, fig. 1; table 7). The precipitates include jarosite and amorphous Fe oxyhydroxide from Ellamar, amorphous Fe oxyhydroxide from Threeman, and amorphous Fe oxyhydroxide, ferrihydrite, and schwertmannite from Beatson. Precipitates occurring in the form of loose, flocculant coatings were harvested using a syringe and concentrated in the field by repetitive decanting. Thicker accumulations were either scraped gently from rocks using a stainless steel spatula or were scooped directly into receptacles (polyethylene jars or plastic heavy-duty zippered bags). Most precipitate samples contain small amounts of sedimentary detritus. With three jarosite-bearing samples from Ellamar, an attempt was made to separate the precipitate from the heavy-mineral fraction of the sediment. In this procedure, the sample was stirred in a graduated cylinder containing deionized water. The jarosite-rich suspension was decanted onto analytical filter paper and air dried before analysis. Eleven precipitate samples from the three mine sites were analyzed in laboratories of the U.S. Geological Survey (USGS) in Denver, Colorado (table 8). Major and trace elements were determined by inductively coupled plasma-mass spectrometry following multiacid (HCl-HNO3-HClO4-HF) digestion (Briggs and Meier, 2002), except for mercury, which was analyzed by cold-vapor atomic absorption spectroscopy (Brown and others, 2002a). X-ray diffraction (XRD) analyses were performed on powdered samples (<200 mesh) by S. Sutley of the USGS. Additional details regarding sample preparation and detection limits are found in Taggert (2002). Discussions of the precipitate chemistry and associated microbial communities are presented in Koski and others (2008) and Foster and others (2008), respectively.

Alaska↗
USGS2007

Chemical data for rock, sediment, biological, precipitate, and water samples from abandoned copper mines in Prince William Sound, Alaska

Introduction In the early 20th century, approximately 6 million metric tons of copper ore were mined from numerous deposits located along the shorelines of fjords and islands in Prince William Sound, Alaska. At the Beatson, Ellamar, and Threeman mine sites (fig. 1), rocks containing Fe, Cu, Zn, and Pb sulfide minerals are exposed to chemical weathering in abandoned mine workings and remnant waste piles that extend into the littoral zone. Field investigations in 2003 and 2005 as well as analytical data for rock, sediment, precipitate, water, and biological samples reveal that the oxidation of sulfides at these sites is resulting in the generation of acid mine drainage and the transport of metals into the marine environment (Koski and others, 2008; Stillings and others, 2008). At the Ellamar and Threeman sites, plumes of acidic and metal-enriched water are flowing through beach gravels into the shallow offshore environment. Interstitial water samples collected from beach sediment at Ellamar have low pH levels (to ~3) and high concentrations of metals including iron, copper, zinc, cobalt, lead, and mercury. The abundant precipitation of the iron sulfate mineral jarosite in the Ellamar gravels also signifies a low-pH environment. At the Beatson mine site (the largest copper mine in the region) seeps containing iron-rich microbial precipitates drain into the intertidal zone below mine dumps (Foster and others, 2008). A stream flowing down to the shoreline from underground mine workings at Beatson has near-neutral pH, but elevated levels of zinc, copper, and lead (Stillings and others, 2008). Offshore sediment samples at Beatson are enriched in these metals. Preliminary chemical data for tissue from marine mussels collected near the Ellamar, Threeman, and Beatson sites reveal elevated levels of copper, zinc, and lead compared to tissue in mussels from other locations in Prince William Sound (Koski and others, 2008). Three papers presenting results of this ongoing investigation of sulfide oxidation in Prince William Sound are in press. Koski and others (2008) provide an overview of rock alteration, surface water chemistry, and the distribution of metals at the Ellamar, Threeman, and Beatson mine sites. Based on a 60-day, stream-discharge experiment at Beatson in 2005, Stillings and others (2008) analyze changes in water chemistry during storm events and the flux of metals to the shoreline. Foster and others (2008) investigate the biomass and diversity of microbial communities present in surface waters (streams, seeps, pore waters) using fatty acid methyl ester (FAMES) data and principal component analysis. The publications cited above contain a subset of the total chemical data for rock, sediment, biological, precipitate, and water samples collected from the three mine sites in 2003 and 2005. The purpose of this report is the presentation of complete chemical data sets for all samples collected during the two field periods of fieldwork. Data for a small number of samples collected at two other mines (Schlosser and Fidalgo, fig. 1), visited in 2003, are also included in the tables.

Alaska↗
USGS2007

Chemical data for rock, sediment, biological, precipitate, and water samples from abandoned copper mines in Prince William Sound, Alaska

In the early 20th century, approximately 6 million metric tons of copper ore were mined from numerous deposits located along the shorelines of fjords and islands in Prince William Sound, Alaska. At the Beatson, Ellamar, and Threeman mine sites (fig. 1), rocks containing Fe, Cu, Zn, and Pb sulfide minerals are exposed to chemical weathering in abandoned mine workings and remnant waste piles that extend into the littoral zone. Field investigations in 2003 and 2005 as well as analytical data for rock, sediment, precipitate, water, and biological samples reveal that the oxidation of sulfides at these sites is resulting in the generation of acid mine drainage and the transport of metals into the marine environment (Koski and others, 2008; Stillings and others, 2008). At the Ellamar and Threeman sites, plumes of acidic and metal-enriched water are flowing through beach gravels into the shallow offshore environment. Interstitial water samples collected from beach sediment at Ellamar have low pH levels (to ~3) and high concentrations of metals including iron, copper, zinc, cobalt, lead, and mercury. The abundant precipitation of the iron sulfate mineral jarosite in the Ellamar gravels also signifies a low-pH environment. At the Beatson mine site (the largest copper mine in the region) seeps containing iron-rich microbial precipitates drain into the intertidal zone below mine dumps (Foster and others, 2008). A stream flowing down to the shoreline from underground mine workings at Beatson has near-neutral pH, but elevated levels of zinc, copper, and lead (Stillings and others, 2008). Offshore sediment samples at Beatson are enriched in these metals. Preliminary chemical data for tissue from marine mussels collected near the Ellamar, Threeman, and Beatson sites reveal elevated levels of copper, zinc, and lead compared to tissue in mussels from other locations in Prince William Sound (Koski and others, 2008). Three papers presenting results of this ongoing investigation of sulfide oxidation in Prince William Sound are in press. Koski and others (2008) provide an overview of rock alteration, surface water chemistry, and the distribution of metals at the Ellamar, Threeman, and Beatson mine sites. Based on a 60-day, stream-discharge experiment at Beatson in 2005, Stillings and others (2008) analyze changes in water chemistry during storm events and the flux of metals to the shoreline. Foster and others (2008) investigate the biomass and diversity of microbial communities present in surface waters (streams, seeps, pore waters) using fatty acid methyl ester (FAMES) data and principal component analysis. The publications cited above contain a subset of the total chemical data for rock, sediment, biological, precipitate, and water samples collected from the three mine sites in 2003 and 2005. The purpose of this report is the presentation of complete chemical data sets for all samples collected during the two field periods of fieldwork. Data for a small number of samples collected at two other mines (Schlosser and Fidalgo, fig. 1), visited in 2003, are also included in the tables.

Alaska↗
USGS2004

Stratiform barite deposits in the Roberts Mountains allochthon, Nevada: A review of potential analogs in modern sea-floor environments

The United States is a net importer of barite, a critical mineral for the oil and gas industry; more than 80 percent of current domestic consumption of barite is imported from China. Nearly all of the domestic production of barite comes from stratiform deposits in Nevada. The 'modern analogs' approach adopted in this review can contribute to improving deposit models and the long-term resource picture in the United States. Massive barite deposits in Nevada are interlayered with deep-water siliceous sedimentary strata of Paleozoic age within the Roberts Mountains Allochthon. Although the barite deposits formed along the long-lived, tectonically active margin of western North America before the Antler orogeny, uncertainty still exists regarding key aspects of their genesis, especially with respect to tectonic setting and depositional processes. Proposed tectonic settings include a continental slope adjacent to an ocean basin, and a rifted basin formed on continental crust. A margin dominated by other stress configurations and strike-slip faulting may also have been present during the Paleozoic. Hypotheses for the genesis of sediment-hosted, stratiform barite deposits in Nevada can be grouped into two categories: (1) a synsedimentary hydrothermal model and (2) an ocean-circulation/productivity-zone model. Both models include a stage involving bacterial reduction of seawater sulfate. Disseminated, diagenetic, and hydrothermal barite deposits are widespread features of the modern ocean. In the Pacific Ocean, disseminated barite deposits (max 9 weight percent BaSO4) are forming below high-productivity zones (for example, in equatorial belts) and on the flanks of ocean ridges (as fallout of 'black smoker' particles). Massive barite deposits of diagenetic (in the subsea floor and at cold seeps) and hydrothermal origins are present in several sediment-covered tectonic settings, including ocean ridges (Escanaba Trough and Guaymas Basin), oceanic transform faults (Blanco Fracture Zone), marginal basins (Sea of Okhotsk), convergent margins (Peru, Oregon, Alaska), and transform margins (California Continental Borderland). Both hydrothermal and diagenetic barite deposits may be present in some environments (for example, the California California Borderland). On the basis of a consideration of tectonic settings and a comparison of deposit attributes (associated rock types, size, structure), mineralogy (BaSO4 content, SiO2 content), and geochemistry (S- and Sr-isotopic ratios) for modern and ancient massive barite deposits, cold seeps along transform margins (or, possibly, marginal basins) represent the most promising present-day metallogenetic analogs for stratiform barite. Hydrothermal systems can also produce high-grade barite, but the ubiquity of associated sulfide mineralization on the modern sea floor (and the paucity of sulfides in Nevada deposits) is problematic. On the basis of data from modern barite deposits, the presence of vent-specific faunas (tubeworms) and the variation in d34S values for barite (related to bacterial reduction of seawater sulfate) may not permit discrimination between a diagenetic or hydrothermal origin for ancient barite deposits.

Nevada↗
USGS2000

Recent tectonics of the Blanco Ridge, eastern blanco transform fault zone

Bathymetric, hydro-acoustic, seismic, submersible, and gravity data are used to investigate the active tectonics of the eastern Blanco Transform Fault Zone (BTFZ). The eastern BTFZ is dominated by the ∼150 km long transform-parallel Blanco Ridge (BR) which is a right-lateral strike-slip fault bordered to the east and west by the Gorda and Cascadia Depressions. Acoustic locations, fault-parameter information, and slip vector estimates of 43 earthquakes ( M w ≥3.8) that occurred along the eastern BTFZ over the last 5 years reveal that the Blanco Ridge is a high-angle right-lateral strike-slip fault, with a small component of dip-slip motion, where the Juan de Fuca plate is the hanging wall relative to the Pacific plate. Furthermore, the Cascadia and Gorda basins are undergoing normal faulting with extension predominantly oblique to the transform trend. Seafloor submersible observations agree with previous hypotheses that the active transform fault trace is the elongate basin that runs the length of the BR summit. Brecciated and undeformed basalt, diabase, and gabbro samples were collected at the four submersible survey sites along the Blanco Ridge. These petrologic samples indicate the Blanco Ridge is composed of an ocean crustal sequence that has been uplifted and highly fractured. The petrologic samples also appear to show an increase in elevation of the crustal section from east to west along the Blanco Ridge, with gabbros exposed at a shallower depth farther west along the southern (Pacific plate side) BR ridge flank. Further supporting evidence for BR uplift exists in the seismic reflection profiles across the BR showing uplift of turbidite sequences along the north and south ridge base, and gravity and magnetics profiles that indicate possible basement uplift and a low-density zone centered on the ridge's Pacific plate side. The BR formation mechanism preferred here is first, uplift achieved partially through strike-slip motion (with a small dip-slip component). Second, seawater penetration along the fault into the lower crust upper mantle, which then enhanced formation and intrusion of a mantle-derived serpentinized-peridotite diapir into the shallow ocean crust, causing further uplift along the fault.

Marine Geophysical Research↗
USGS1993

Massive sulfide metallogenesis at a late Mesozoic sediment-covered spreading axis: Evidence from the Franciscan complex and contemporary analogues

The Island Mountain deposit, an anomalous massive sulfide in the Central belt of the Franciscan subduction complex, northern California Coast Ranges, formed during hydrothermal activity in a sediment-dominated paleo-sea-floor environment. Although the base of the massive sulfide is juxtaposed against a 500-m-wide melange band, its gradational upper contact within a coherent sequence of sandstone, siltstone, and mudstone indicates that hydrothermal activity was concurrent with turbidite deposition. Accumulations of sulfide breccia and clastic sulfide were produced by mass wasting of the sulfide mound prior to burial by turbidites. The bulk composition of sulfide samples (pyrrhotite rich; high Cu, As, and Au contents; radiogenic Pb isotope ratios) is consistent with a hydrothermal system dominated by fluid-sediment interaction. On the basis of a comparison with possible contemporary tectonic analogues at the southern Gorda Ridge and the Chile margin triple junction, we propose that massive sulfide mineralization in the Central belt of the Franciscan complex resulted from hydrothermal activity at a late Mesozoic sediment-covered ridge axis prior to collision with the North American plate.

California↗