ALBERT

Description: Hydrothermal fluids responsible for the formation of volcanogenic massive sulfides may transport gold in solution as Au(HS) 2 (super -) at low temperatures (〈350 degrees C), near neutral pH, and high concentrations of H 2 S (10 (super -3) -10 (super -2) m). To a lesser extent gold may be transported as AuCl 2 (super -) at higher temperatures (〉 or =350 degrees C), low pH, and elevated salinities (〉 or =1 m NaCl). The documented fluid chemistry of active hydrothermal vents on the modern seafloor confirms that gold transport is mainly due to Au(HS) 2 (super -) , and the calculated solubility of gold as Au(HS) 2 (super -) is highest in low-temperature (150 degrees -250 degrees C) vent fluids at elevated oxygen and sulfur activities. Sulfides which coprecipitate with gold commonly have properties which can be related to the temperature and sulfidation state of the hydrothermal fluids and therefore reflect conditions which were favorable for the transport or deposition of gold as Au(HS) 2 (super -) .A comparison of gold grades with sulfide mineral equilibria and the FeS contents in sphalerite from a variety of deposits indicates that gold enrichment is closely related to the temperature-a (sub S 2 ) conditions in the ore-forming fluids. Sea-floor sulfides range from sulfur-rich, pyrite-marcasite assemblages to relatively sulfur-deficient, pyrrhotite-isocubanite assemblages, with coexisting sphalerite containing 0 to 55 mole percent FeS. Significant gold enrichment occurs exclusively in low-temperature (〈300 degrees C) pyritic sulfides, together with sulfur-rich trace minerals and Fe-poor sphalerite. Bulk gold contents range from 〈0.5 ppm Au in sulfides with sphalerite containing 10 to 55 mole percent FeS up to 6.7 ppm Au in sulfides with sphalerite containing 〈10 mole percent FeS. Fluid inclusions in Fe-poor sphalerite (〈5 mole % FeS) from one gold-rich deposit (avg 4.9 ppm Au) have trapping temperatures of 235 degrees + or - 13 degrees C (Hannington and Scott, 1988). Low-temperature ores with high gold contents are also common in Phanerozoic Zn-Cu-Pb deposits in Japan (Kosaka, Furutobe, Shakanai) and similar deposits in British Columbia (HW mine, Lynx, Seneca). Gold-bearing polymetallic sulfides contain sulfur-rich mineral assemblages (e.g., bornite + pyrite) and recognizable trace mineral equilibria which indicate a high a (sub S 2 ) (e.g., argentite-electrum, tennantite-enargite, covellite-digenite). Zn-Cu-Pb ores formed at 200 degrees to 300 degrees C typically contain Fe-poor sphalerite (〈1 mole % FeS) and gold grades of i to 3 ppm Au, whereas Cu-rich ores formed at 〉300 degrees C contain Ferich sphalerite (1-5 mole % FeS) and gold grades 〈 1 ppm Au. Archean Cu-Zn deposits at Noranda, Quebec, consist mainly ofpyrite-pyrrhotite ores containing 0.5 to 1 ppm Au together with Fe-rich sphalerite (10-12 mole % FeS). However, pyritic ores which occur stratigraphically up-section commonly contain 1 to 3 ppm Au and relatively Fe-poor sphalerite (5 mole % FeS). Different sulfide mineral equilibria and FeS contents in sphalerite are interpreted to reflect the same physical and chemical conditions which influence gold grades and suggest that petrologic indicators of the sulfidation state may be useful guides to gold mineralization in volcanogenic massive sulfides.

Description: The discovery of metal-depositing hot springs on the sea floor, and especially their link to chemosynthetic life, was among the most compelling and significant scientific advances of the twentieth century. More than 300 sites of hydrothermal activity and sea-floor mineralization are known on the ocean floor. About 100 of these are sites of high-temperature venting and polymetallic sulfide deposits. They occur at mid-ocean ridges (65%), in back-arc basins (22%), and on submarine volcanic arcs (12%). Although high-temperature, 350°C, black smoker vents are the most recognizable features of sea-floor hydrothermal activity, a wide range of different styles of mineralization has been found. Different volcanic substrates, including mid-ocean ridge basalt, ultramafic intrusive rocks, and more evolved volcanic suites in both oceanic and continental crust, as well as temperature-dependent solubility controls, account for the main geochemical associations found in the deposits. Although end-member hydrothermal fluids mainly originate in the deep volcanic basement, the presence of sediments and other substrates can have a large effect on the compositions of the vent fluids. In arc and backarc settings, vent fluid compositions are broadly similar to those at mid-ocean ridges, but the arc magmas also supply a number of components to the hydrothermal fluids. The majority of known black smoker vents occur on fast-spreading mid-ocean ridges, but the largest massive sulfide deposits are located at intermediate- and slow-spreading centers, at ridge-axis volcanoes, in deep backarc basins, and in sedimented rifts adjacent to continental margins. The range of deposit sizes in these settings is similar to that of ancient volcanic-associated massive sulfide (VMS) deposits. Detailed mapping, and in some cases drilling, indicates that a number of deposits contain 1 to 5 million tons (Mt) of massive sulfide (e.g., TAG hydrothermal field on the Mid-Atlantic Ridge, deposits of the Galapagos Rift, and at 13°N on the East Pacific Rise). Two sediment-hosted deposits, at Middle Valley on the Juan de Fuca Ridge and in the Atlantis II Deep of the Red Sea, are much larger (up to 15 and 90 Mt, respectively). In the western Pacific, high-temperature hydrothermal systems occur mainly at intraoceanic back-arc spreading centers (e.g., Lau basin, North Fiji basin, Mariana trough) and in arc-related rifts at continental margins (e.g., Okinawa trough). In contrast to the mid-ocean ridges, convergent margin settings are characterized by a range of different crustal thicknesses and compositions, variable heat flow regimes, and diverse magma types. These variations result in major differences in the compositions and isotopic systematics of the hydrothermal fluids and the mineralogy and bulk compositions of the associated mineral deposits. Intraoceanic back-arc basin spreading centers host black smoker vents that, for the most part, are very similar to those on the mid-ocean ridges. However, isotopic data from both the volcanic rocks and the sulfide deposits highlight the importance of subduction recycling in the origin of the magmas and hydrothermal fluids. Back-arc rifts in continental margin settings are typically sediment-filled basins, which derive their sediment load from the adjacent continental shelf. This has an insulating effect that enhances the high heat flow associated with rifting of the continental crust and also helps to preserve the contained sulfide deposits. Large hydrothermal systems have developed where initial rifting of continental crust or locally thickened arc crust has formed large calderalike sea-floor depressions, similar to those that contained major VMS-forming systems in the geologic record. Hydrothermal vents also occur in the summit calderas of submarine volcanoes at the volcanic fronts of arcs. However, this contrasts with the interpreted settings of most ancient VMS deposits, which are considered to have formed mainly during arc rifting. Hydrothermal vents associated with arc volcanoes show clear evidence of the direct input of magmatic volatiles, similar to magmatic-hydrothermal systems in subaerial volcanic arcs. Several compelling examples of submarine epithermal-style mineralization, including gold-base metal veins, have been found on submarine arc volcanoes,and this type of mineralization may be more common than is presently recognized. Mapping and sampling of the sea floor has dramatically improved geodynamic models of different submarine volcanic and tectonic settings and has helped to establish a framework for the characterization of many similar ancient terranes. Deposits forming at convergent margins are considered to be the closest analogs of ancient VMS. However, black smokers on the mid-ocean ridges continue to provide critically important information about metal transport and deposition in sea-floor hydrothermal systems of all types. Ongoing sea-floor exploration in other settings is providing clues to the diversity of mineral deposit types that occur in different environments and the conditions that are favorable for their formation.

Description: The Monowai volcanic center is located at the midpoint along the ~2,530-km-long Tonga-Kermadec arc system. The Monowai volcanic center is comprised of a large elongate caldera (Monowai caldera area ~35 km2; depth to caldera floor 1,590 m), which has formed within an older caldera some 84 km2 in area. To the south of this nested caldera system is a large composite volcano, Monowai cone, which rises to within ~100 m of the sea surface and which has been volcanically active for the past several decades. Mafic volcanic rocks dominate the Monowai volcanic center; basalts are the most common rock type recovered from the cone, whereas basaltic andesites are common within the caldera. Hydrothermal plume mapping has shown at least three major hydrothermal systems associated with the caldera and cone: (1) the summit of the cone, (2) low-temperature venting (〈60°C; Mussel Ridge) on the southwestern wall of the caldera, and (3) a deeper caldera source with higher temperature venting that has yet to be observed. The cone summit plume shows large anomalies in pH (a shift of −2.00 pH units) and δ3He (≤358%), and noticeable H2S (up to 32 μm), and CH4 (up to 900 nm). The summit plume is also metal rich, with elevated total dissolvable Fe (TDFe up to 4,200 nm), TDMn (up to 412 nm), and TDFe/TDMn (up to 20.4). Particulate samples have elevated Fe, Si, Al, and Ti consistent with addition to the hydrothermal fluid from acidic water-rock reaction. Plumes extending from ~1,000- to 1,400-m depth provide evidence for a major hydrothermal vent system in the caldera. The caldera plume has lower values for TDFe and TDMn, although some samples show higher TDMn concentrations than the cone summit plume; caldera plume samples are also relatively gas poor (i.e., no H2S detected, pH shift of −0.06 pH units, CH4 concentrations up to 26 nm). The composition of the hydrothermal plumes in the caldera have higher metal contents than the sampled vent fluids along Mussel Ridge, requiring that the source of the caldera plumes is at greater depth and likely of higher temperature. Minor plumes detected as light scattering anomalies but with no 3He anomalies down the northern flank of the Monowai caldera most likely represent remobilization of volcanic debris from the volcano flanks. We believe the Monowai volcanic center is host to a robust magmatic-hydrothermal system, with significant differences in the style and composition of venting at the cone and caldera sites. At the cone, the large shifts in pH, very high δ3He% values, elevated TDFe and TDFe/TDMn, and the H2S- and CH4-rich nature of the plume fluids, together with elevated Ti, P, V, S, and Al in hydrothermal particulates, indicates significant magmatic volatile ± metal contributions in the hydrothermal system coupled with aggressive acidic water-rock interaction. By contrast, the caldera has low TDFe/TDMn in hydrothermal plumes; however, elevated Al and Ti contents in caldera particulate samples, combined with the presence of alunite, pyrophyllite, sulfide minerals, and native sulfur in samples from Mussel Ridge suggest past, and perhaps recent, acid volatile-rich venting and active Fe sulfide formation in the subsurface.

Description: Bulk chemical analyses of 48 samples of hydrothermal precipitates from seven polymetallic sulfide deposits at sea-floor spreading centers in the eastern Pacific reveal distinct patterns of gold enrichment. High gold contents are found in samples from two sulfide deposits: the Axial Seamount (45 degrees 57' N, 130 degrees 02' W), and the southern Explorer Ridge (49 degrees 45.6' N, 130 degrees 16.2' W). A large, 160-kg sample composed of silica, barite, and sphalerite from the top of the Axial Seamount deposit gives analyses up to 6,700 ppb Au, averaging 4,900 ppb Au. Similar material from the southern Explorer Ridge gives analyses up to 1,500 ppb Au, averaging 660 ppb Au. Detailed mineralogical studies together with bulk chemical analyses of a wide range of samples from these two sites reveal strong elemental associations and paragenetic controls on gold deposition. Gold at concentrations of about 200 ppb is associated with high Cu (〉1 wt %) and Mo (up to 470 ppm); at concentrations 〉 800 ppb, with high Zn (〉10 wt %), Ba (〉3 wt %), and SiO 2 (〉20 wt %); and at concentrations 〉 1,200 ppb, with high Pb (〉0.1 wt %), Ag (〉100 ppm), As (〉300 ppm), and Sb (50-100 ppm). Samples with the highest gold values from both locations contain late, sinterlike, low-temperature sulfosalts of Pb, As, Sb, Ag, and S in a matrix of amorphous silica. These sulfosalts are the probable repositories of the gold.Published analyses of Au-poor (〈200 ppb Au) samples from other basalt-hosted sea-floor deposits (21 degrees N, Galapagos rift, southern Juan de Fuca Ridge, Endeavour Ridge) are high in metals and sulfur but low in silica relative to samples from the Axial Seamount and the southern Explorer Ridge. Hydrothermal deposits in the Guaymas basin are underlain by sediments that are enriched in gold relative to midocean ridge basalts, but samples from these deposits do not reflect this enrichment and give average analyses 〈200 ppb Au. It is suggested that gold is preconcentrated to about 200 ppb in high-temperature (〉300 degrees C), Cu-Fe-rich sulfides and subsequently remobilized by late, sustained, low-temperature (〈250 degrees C) fluids and concentrated in SiO 2 -Ba-Zn-rich precipitates near the surface. Suitable fluid chemistry is required to mobilize the gold and a favorable precipitation mechanism is needed to concentrate it.These observations could explain the occurrence of high gold concentrations in selected ore types of some ancient massive sulfide deposits on land.

Description: The Jbel Tirremi fluorite-barite sulfide deposit in northeastern Morocco is hosted in a Jurassic-aged structurally high carbonate platform known as the Jbel Tirremi dome. The host rocks consist of unmetamorphosed, flat-lying early Jurassic dolomitized limestones, locally intruded by Eocene lamprophyre dikes. The orebodies consist mostly of fluorite and barite, and occur as open-space fillings and partial to massive replacement of the enclosing medium- to coarse-grained dolomitized limestones. The ore mineralogy is dominated by fluorite of different colors and habits, barite, and, to a lesser extent, sulfides. Rare earth element compositions along with fluid inclusion, halogen and isotopic data suggest that the fluorite barite mineralization and the spatially associated Eocene alkaline magmatism are petrogenetically unrelated, pointing instead to the regional circulation of hydrothermal basinal brines mixed to various degrees with meteoric water in a dominantly closed rock-buffered system at progressively higher temperatures and fluid/rock ratios. In this respect, fluid inclusion microthermometric measurements show that the ore-bearing hydrothermal system developed in two separate stages of fluorite-barite mineralization, as also revealed by isotopic data. Both stages precipitated from saline fluids at shallow crustal levels (i.e., 〈5 km), and were related, in varying degrees, to different stages of basin evolution and salt dome growth (salt mobilization and mineralization). During the first stage, the ore fluid was a highly saline aqueous brine with a total salinity up to 44.2 wt % NaCl + KCl equiv, at temperatures 〉= 82 degrees C and possibly up to 218 degrees C, whereas in the second stage the mineralizing fluid had a similar temperature range, but lower salinities (similar to 20-10 wt % NaCl equiv). The recorded high salinities are interpreted to represent the involvement of a mixture of halite dissolution water and evaporated seawater component. Oxygen (delta O-18 = 21.7 to 29.6%0 V-SMOW) and carbon (delta C-13 = -7.9 to 0.2%0 V-PDB) isotope data along with strontium (Sr-87/Sr-86 = 0.70300-070789) and lead (Pb-206/Pb-204 = 17.961-20.96, Pb-207/Pb-204, 15.511-15.697, Pb-208/Pb-204 = 37.784-39.993) isotope ratios suggest the involvement of a mixture of oil-bearing fluids, basinal brines, and meteoric fluids that interacted extensively with the early Jurassic host carbonates, the underlying Triassic salt-bearing diapir, associated siliciclastic rocks, and the highly fractionated and greisenized Hercynian granitic crystalline basement, resulting in the release of fluoride, metals, and other constituents to form the Jbel Tirremi deposit. Petroleum-bearing fluid, released from overpressured portions of the Guercif Basin at lithostatic pressures, and bittern brines dominated the first stage of mineralization. Mixing of saline, oxidized, CaCl2- and sulfate-rich bittern brine with oil-bearing fluid resulted in fluorite precipitation of stage I. Conversely, during the second stage of mineralization, the hydrothermal system was open to the influx of oxidized meteoric water as a consequence of the upward migration of the Triassic salt-bearing diapir and associated pressure decrease. The shift from stage I to stage II is associated with the evolution of the system from lithostatic to mostly hydrostatic pressure conditions. Stage I mineralization is thought to have occurred during the Late Miocene in response to rapid sedimentation and high subsidence rates and subsequent hydrocarbon migration associated with the outward migration of the Rif thrust front. Conversely, stage II mineralization occurred coevally with the uplift phase during Tortonian time.

Description: The LaRonde Penna Au-rich volcanogenic massive sulfide (VMS) deposit is the largest Au deposit currently mined in Canada (58.8 Mt at 4.31 g/t, containing 8.1 Moz of Au). It is part of the Doyon-Bousquet-LaRonde mining camp located in the eastern part of the Blake River Group of the Abitibi greenstone belt which is host to several of the world’s most important, present and past, Au-rich VMS deposits (e.g., Horne, Quemont, Bousquet, Bousquet 2-Dumagami). The LaRonde Penna deposit consists of massive to semimassive sulfide lenses (Au-Zn-Ag-Cu-Pb), stacked in the upper part of a steeply dipping, south-facing homoclinal volcanic sequence composed of extensive tholeiitic basaltic flows (Hébécourt Formation) overlain by tholeiitic to transitional, mafic to intermediate, effusive and volcaniclastic units at the base (lower member of the Bousquet Formation) and transitional to calc-alkaline, intermediate to felsic, effusive and intrusive rocks on top (upper member of the Bousquet Formation). The mafic to felsic volcanism of the Hébécourt Formation and of the lower member of the Bousquet Formation formed an extensive submarine basement or platform on which the intermediate to felsic rocks of the upper member of the Bousquet Formation were emplaced at restricted submarine eruptive centers or as shallow composite intrusive complexes. The submarine felsic volcanic rocks of the upper member of the Bousquet Formation are characterized by dacitic to rhyodacitic autoclastic (flow breccia) deposits that are cut and overlain by rhyodacitic and rhyolitic domes and/or partly extrusive cryptodomes and by intermediate to mafic sills and dikes. This volcanic architecture is thought to have been responsible for internal variations in ore and alteration styles, not only from one lens to another, but also along a single mineralized horizon or lens. In the upper part of the mine, the 20 North lens comprises a transposed pyrite-chalcopyrite (Au-Cu) stockwork (20N Au zone) overlain by a pyrite-sphalerite-galena-chalcopyrite-pyrrhotite (Zn-Ag-Pb) massive sulfide lens (20N Zn zone). The latter was formed, at least in part, by replacement of footwall rhyodacitic autoclastic deposits emplaced within a subbasin located between two rhyolite domes or cryptodomes. The 20N Zn zone tapers with depth in the mine and gives way to the 20N Au zone. At depth in the mine, the 20N Au zone consists of semimassive sulfides (Au-rich pyrite and chalcopyrite) enclosed by a large aluminous alteration halo on the margin of a large rhyolitic dome or cryptodome. U-Pb zircon geochronology gives ages of 2698.3 ± 0.8 and 2697.8 ± 1 Ma for the footwall and hanging-wall units of the 20 North lens, respectively. Thus, the formation of the 20 North lens was coeval with other VMS deposits in the Bousquet Formation and in the uppermost units of the Blake River Group. Although deformation and metamorphism have affected the primary mineral assemblages and the original geometry of the deposit, these events were not responsible for the different auriferous ore zones and alteration at LaRonde Penna. Studies of the LaRonde Penna deposit show that the hydrothermal system evolved in time and space from near-neutral seawater-dominated hydrothermal fluids, responsible for Au-Cu-Zn-Ag-Pb mineralization, to highly acidic fluids with possible direct magmatic contributions, responsible for Au ± Cu-rich ore and aluminous alteration. The different ore types and alteration reflect the evolving local volcanic setting described in this study.

Description: Clark volcano of the Kermadec arc, northeast of New Zealand, is a large stratovolcano comprised of two coalescing volcanic cones; an apparently younger, more coherent, twin-peaked edifice to the northwest and a relatively older, more degraded and tectonized cone to the southeast. High-resolution water column surveys show an active hydrothermal system at the summit of the NW cone largely along a ridge spur connecting the two peaks, with activity also noted at the head of scarps related to sector collapse. Clark is the only known cone volcano along the Kermadec arc to host sulfide mineralization. Volcano-scale gravity and magnetic surveys over Clark show that it is highly magnetized, and that a strong gravity gradient exists between the two edifices. Modeling suggests that a crustal-scale fault lies between these two edifices, with thinner crust beneath the NW cone. Locations of regional earthquake epicenters show a southwest-northeast trend bisecting the two Clark cones, striking northeastward into Tangaroa volcano. Detailed mapping of magnetics above the NW cone summit shows a highly magnetized “ring structure” ~350 m below the summit that is not apparent in the bathymetry; we believe this structure represents the top of a caldera. Oblate zones of low (weak) magnetization caused by hydrothermal fluid upflow, here termed “burn holes,” form a pattern in the regional magnetization resembling Swiss cheese. Presumably older burn holes occupy the inner margin of the ring structure and show no signs of hydrothermal activity, while younger burn holes are coincident with active venting on the summit. A combination of mineralogy, geochemistry, and seafloor mapping of the NW cone shows that hydrothermal activity today is largely manifest by widespread diffuse venting, with temperatures ranging between 56° and 106°C. Numerous, small (≤30 cm high) chimneys populate the summit area, with one site host to the ~7-m-tall “Twin Towers” chimneys with maximum vent fluid temperatures of 221°C (pH 4.9), consistent with δ34Sanhydrite-pyrite values indicating formation temperatures of ~228° to 249°C. Mineralization is dominated by pyrite-marcasite-barite-anhydrite. Radiometric dating using the 228Ra/226Ra and 226Ra/Ba methods shows active chimneys to be 〈20 with most 〈2 years old. However, the chimneys at Clark show evidence for mixing with, and remobilizing of, barite as old as 19,000 years. This is consistent with Nd and Sr isotope compositions of Clark chimney and sulfate crust samples that indicate mixing of ~40% seawater with a vent fluid derived from low K lavas. Similarly, REE data show the hydrothermal fluids have interacted with a plagioclase-rich source rock. A holistic approach to the study of the Clark hydrothermal system has revealed a two-stage process whereby a caldera-forming volcanic event preceded a later cone-building event. This ensured a protracted (at least 20 ka yrs) history of hydrothermal activity and associated mineral deposition. If we assume at least 200-m-high walls for the postulated (buried) caldera, then hydrothermal fluids would have exited the seafloor 20 ka years ago at least 550 m deeper than they do today, with fluid discharge temperatures potentially much hotter (~350°C). Subsequent to caldera infilling, relatively porous volcaniclastic and other units making up the cone acted as large-scale filters, enabling ascending hydrothermal fluids to boil and mix with seawater subseafloor, effectively removing the metals (including remobilized Cu) in solution before they reached the seafloor. This has implications for estimates for the metal inventory of seafloor hydrothermal systems pertaining to arc hydrothermal systems.

Description: Sea-floor imagery, volcanic rock, massive sulfide, and hydrothermal plume samples (δ3He, pH, dissolved Fe and Mn, and particulate chemistry) have been collected from the Rumble II West volcano, southern Kermadec arc, New Zealand. Rumble II West is a caldera volcano with an ∼3-km-diameter summit depression bounded by ring faults with a resurgent central cone. Rocks recovered to date are predominantly mafic in composition (i.e., basalt to basaltic andesite) with volumetrically lesser intermediate rocks (i.e., andesite). On the basis of its size, geometry, volcanic products, and composition, Rumble II West can be classified as a mafic caldera volcano. Rumble II West has a weak hydrothermal plume signature characterized by a small but detectable δ3He anomaly (25%). Time-series light scattering data though, obtained from vertical casts and tow-yos, do show that hydrothermal activity has increased in intensity between 1999 and 2011. Massive sulfides recovered from the eastern caldera wall and eastern flank of the central cone are primarily comprised of barite and chalcopyrite, with lesser sphalerite, pyrite, and traces of galena. The weak hydrothermal plume signal indicates that the volcano is in a volcanic-hydrothermal quiescent stage compared to other volcanoes along the southern Kermadec arc, although the preponderance of barite with massive sulfide mineralization indicates higher temperature venting in the past. Of the volcanoes along the Kermadec-Tonga arc known to host massive sulfides (i.e., Clark, Rumble II West, Brothers, Monowai, Volcano 19, and Volcano 1), the majority (five out of six) are dominantly mafic in composition and all but one of these mafic volcanoes form moderate-size to large calderas. To date, mafic calderas have been largely ignored as hosts to sea-floor massive sulfide deposits. That 75% of the presently known massive sulfide-bearing calderas along the arc are mafic in composition (the dacitic Brothers volcano is the exception) has important implications for sea-floor massive sulfide mineral exploration in the modern oceans and ancient rock record on land.

Description: Middle Valley is a sediment-covered rift near the northern end of Juan de Fuca Ridge. Hydrothermal fluids are presently being discharged at two vent fields about 3 km apart, Bent Hill and the area of active venting. The hydrothermally active chimneys at both Bent Hill and the area of active venting consist of anhydrite and Mg-rich silicates with minor pyrite, Cu-Fe sulfide, sphalerite, and galena. Hydrothermal discharge in these areas appears to be focused along extensional faults. At the Bent Hill massive sulfide deposit, clastic sulfide layers are interbedded with hydrothermally altered and unaltered hemipelagic and turbiditic sediment along the flanks of the sulfide mound. Sulfide textures and mineralogy suggest that the Bent Hill sulfide mound formed by the build-up and collapse of sulfide chimneys, the resedimentation of sulfide debris and the formation of clastic sulfide layers, and the infilling and replacement of clastic sulfides by hydrothermal fluids near vents. Sulfur isotope values that are consistently more positive than basaltic sulfur support the addition of seawater sulfur. Pb isotope values for the Bent Hill deposit that are transitional between midocean ridge basalt (MORB) and Middle Valley sediments indicate that the sulfides probably formed from fluids which originated in the oceanic crust but which have been modified by reaction with lower temperature (〈273°C)fluids generated in the sedimentary pile, similar to those now venting in Middle Valley.