Entrainment Of Seawater Research Articles

Rafting of Growing Antarctic Sea Ice Enhances In‐Ice Biogeochemical Activity in Winter

AbstractThe study of Antarctic first‐year sea‐ice biogeochemistry has been limited by samples mostly being collected in pack ice during summer, with few winter data available. Measurements from the Antarctic marginal ice zone (AMIZ) have proven even more difficult to obtain. The AMIZ is a broad, circumpolar feature of the Southern Ocean found at different latitudes during the year where light and nutrients are high enough to sustain primary production and influence ecosystem functioning. We present the first biogeochemical data set from growing ice collected in the Atlantic AMIZ during winter 2019, including measurements from young pancake ice (YI) and consolidated first‐year ice (FYI). Measurements of sea‐ice temperature, salinity, crystal structure, δ18O, chlorophyll, and nutrient concentrations were used to investigate the winter sea‐ice habitat and decipher the conditions under which the ice formed and grew. Model simulations support the hypothesis that nutrient accumulation in advancing sea ice cannot be explained by passive seawater entrainment and thermodynamics alone. Our data confirm that winter sea ice is biogeochemically active and accumulates remineralized nutrients. We further propose that mechanical thickening enhances the reservoir of nutrients during the ice growth season. The biogeochemical transition from YI to FYI does not appear to be a linear progression of thickness with habitat space reduction as sea ice consolidates. Instead, FYI bulk biogeochemistry results from multiple cycles of rafting of YI, which conserves the biogeochemical properties of YI in the FYI, ultimately increasing the overall nutrient and chlorophyll content.

Incorporation of the riser-seabed-seawater interaction effects into the trench formation and fatigue response of steel catenary risers in the touchdown zone

The existing Steel Catenary Riser (SCR)-seabed interaction models do not account for the contribution of seawater as a key influential factor. The present study has examined the effect of SCR-seabed-seawater interaction on the trench enlargement and consequently on the fatigue performance of the SCR in the touchdown zone (TDZ). Coupled Eulerian-Lagrangian (CEL) analysis with three domains of SCR, seabed soil, and seawater were performed using ABAQUS. A parametric study was conducted to investigate the impact of seawater interaction along with incorporation of the shear strain rate and softening effects. The conventional bearing capacity approach for analysing pipe penetration into the seabed was also reviewed, and modifications were proposed to account for the effects of water entrainment into the trench. The results obtained from CEL analysis were integrated with a global SCR model to incorporate the SCR-seabed-seawater interaction effects into the fatigue analysis. The study showed that the entrainment of seawater into the trench can be coupled with SCR oscillations to further soften the seabed and erode the trench resulting in an enlarged trench profile affecting the fatigue damage in the TDZ.

Lightning Rings and Gravity Waves: Insights Into the Giant Eruption Plume From Tonga's Hunga Volcano on 15 January 2022

AbstractOn 15 January 2022, Hunga Volcano in Tonga produced the most violent eruption in the modern satellite era, sending a water‐rich plume at least 58 km high. Using a combination of satellite‐ and ground‐based sensors, we investigate the astonishing rate of volcanic lightning (>2,600 flashes min−1) and what it reveals about the dynamics of the submarine eruption. In map view, lightning locations form radially expanding rings. We show that the initial lightning ring is co‐located with an internal gravity wave traveling >80 m s−1 in the stratospheric umbrella cloud. Buoyant oscillations of the plume's overshooting top generated the gravity waves, which enhanced turbulent particle interactions and triggered high‐current electrical discharges at unusually high altitudes. Our analysis attributes the intense lightning activity to an exceptional mass eruption rate (>5 × 109 kg s−1), rapidly expanding umbrella cloud, and entrainment of abundant seawater vaporized from magma‐water interaction at the submarine vent.

Geochemistry of vent fluids from the Daxi Vent Field, Carlsberg Ridge, Indian Ocean: Constraints on subseafloor processes beneath a non-transform offset

The Daxi Vent Field (DVF) is located on a neovolcanic ridge within a non-transform offset at water depths of ∼3500 m, on the Carlsberg Ridge, northwest Indian Ocean. In 2017, we investigated this site using the submersible Jiaolong and collected two fluid samples from orifices of chimneys named “Buddha's Hands” and “A1”, about 37 m apart. Their in-situ measured temperatures are 273 °C and 272 °C, respectively. The Buddha's Hands fluid is highly Cl-enriched (928 mM), while the A1 fluid is Cl-depleted (303 mM). This indicates that they have undergone phase separation. The segregated phases must have remixed during the ascent because the vapor and brine phases sampled cannot be produced by the same phase separation history without other processes. Olivine-rich and/or ultramafic mantle rocks must have been involved during the hydrothermal circulation as evidenced by high dissolved H2 (7.07 mM) and methane (0.884 mM) concentrations, a depletion in B relative to seawater, high Ca and low K, and large positive Eu anomalies. The Fe content in Buddha's Hands fluid is extremely high (11,900 μM) as a result of phase separation, while the Cu concentrations in both fluids are relatively low due to entrainment of seawater which results in precipitation of Cu-rich sulfides in the subseafloor. The concentrations of Zn, Ag, Ga, Sn, Sb, and Cd in A1 vent fluid are significantly elevated due to generation of acidity and remobilization of these elements as Cu-rich sulfides are deposited. The subseafloor processes and associated geochemistry of hydrothermal fluids at the DVF are distinct from other mid-ocean ridge hydrothermal systems due to the specific geologic setting. Hence a hybrid model of hydrothermal circulation is proposed. This study broadens our understanding of the hydrothermal processes occurring in areas of NTO setting and provides more information on mass fluxes discharging from hydrothermal systems and the formation of sulfide deposits.

The effect of high-temperature alteration of oceanic crust on the potassium isotopic composition of seawater

High-temperature hydrothermal alteration of oceanic crust is one of the two main sources of potassium (K) to the oceans, with modern flux estimates ranging roughly from ∼8 to 30 % of the K flux from rivers. Despite the role of high-temperature hydrothermal fluids in the global seawater K budget, little is known about its effect on the K isotopic composition of the oceans. Here we present stable K isotope measurements (δ41KSRM3141a) of globally distributed high-temperature hydrothermal fluids from three mid-ocean ridge systems: the East Pacific Rise (n = 21), the Juan de Fuca Ridge (n = 34), and the Mid-Atlantic Ridge (n = 18). We find a strong correlation between δ41K and Mg/K ratios, consistent with conservative mixing between a high-temperature hydrothermal fluid (i.e., Mg = 0) and seawater as fluids ascend to the seafloor and/or due to seawater entrainment during sampling. The δ41K of end-member hydrothermal fluids is found to range between −0.80 ‰ and 0.07 ‰, with an average value of −0.36 ± 0.30 ‰ (2σ, n = 38). Most (∼76 %) of the variability in end-member fluid δ41K compositions observed here can be explained by high-temperature fluid-rock K exchange, with little (∼0.2 ‰) to no K isotope fractionation between hydrothermal fluid and altered crust. Larger deviations from the average end-member hydrothermal fluid value are likely to result from processes other than high-temperature fluid-rock exchange, such as (1) low-temperature hydrothermal reactions during fluid recharge, (2) reaction of fluids with local sedimentary sources, and (3) phase separation. The K contents of end-member fluids vary considerably, from ∼1 to 38 mM, thus a K-weighted average of −0.37 ± 0.24 ‰ (2σ, n = 38) is estimated to represent the δ41K composition of the global hydrothermal K flux. Our results suggest that K sourced from axial hydrothermal alteration does not contribute to the elevated 41K/39K of seawater compared to bulk silicate Earth (BSE). In addition, subduction of oceanic crust altered under high-temperature conditions is unlikely to be a significant source of K isotopic heterogeneity to Earth’s mantle.

Extending the dataset of fluid geochemistry of the Menez Gwen, Lucky Strike, Rainbow, TAG and Snake Pit hydrothermal vent fields: Investigation of temporal stability and organic contribution

The Menez Gwen, Lucky Strike, Rainbow, TAG (Transatlantic Geotraverse) and Snake Pit hydrothermal vent fields on the Mid-Atlantic Ridge were revisited and resampled for geochemical investigation during the BIOBAZ 2013 and BICOSE 2014 research cruises. Geochemical analysis of the major and minor elements of the hydrothermal fluid and concentrations of gases extends and complements the existing dataset. Our results are consistent with values previously reported and fall within the range of the analytical error. This indicates that the hydrothermal vent field system has remained relatively stable over the last few decades. However, some differences were observed and (i) suggested a recent eruption at Menez Gwen, (ii) supported the occurrence of low-temperature serpentinisation in this same site, (iii) supported a change in the reaction zone or axial magma chamber (AMC) depth at Lucky Strike, (iv) an increase of the temperature at depth at Snake Pit and (v) supported the hypothesis of large seawater entrainment through the TAG hydrothermal mound. Besides, it is possible that small temporal and spatial scale processes may control a significant part of the geochemistry, owing to the fact that some variations in the data could not be interpreted. However, our investigation of the organic geochemistry represents a pioneering addition to research for Menez Gwen, Snake Pit and TAG and a much more comprehensive study for Lucky Strike and Rainbow. Concentrations for a wide variety of semi volatile organic compounds (SVOCs) were obtained for the first time at all sites. Our results showed that a great part of the total organic carbon (TOC) could not be allocated by the total SVOCs studied here, suggesting that other processes/sources of organic carbon remain to be identified. The TAG organic geochemistry seemed entirely based on thermogenic processes whereas mixed processes may occur at the other vent field. The presence of n-alkanes suggested the contribution of a low-temperature fluid at all sites. An additional high-temperature organic matter degradation component was likely present at Menez Gwen and Lucky Strike. Our results also indicated that both abiogenic and biogenic processes produced organic compounds. Therefore, we suggest that a portion of the fatty acids at Menez Gwen and polyaromatic hydrocarbons (PAHs) at Rainbow may be derived from abiogenic processes, whereas biogenic processes could be responsible for the presence of n-fatty acids (n-FAs) at Lucky Strike and Rainbow. Moreover, organic geochemistry data appeared to be helpful in understanding some inorganic processes.

Down-canyon evolution of turbidity currents at a late-glacial ice margin: Halibut Canyon, offshore southeastern Canada

Submarine canyons are the principal conduit for turbidity currents transporting sediment to the deep sea. This study examines the interplay between ice-margin conditions and the style of turbidity currents during deglaciation from 19 to 11 ka. We investigated 7 cores from Halibut Canyon, located seaward of a small ice stream draining the Newfoundland Ice Dome. Cores were X-radiographed for sedimentary structures, sediment provenance was assessed from X-ray fluorescence geochemistry, and age was determined by AMS C-14 dating. High resolution seismic profiles and cores show three phases of canyon evolution: (1) Canyon erosion by plunging hyperpycnal meltwater from shelf-edge ice at maximum ice extent. (2) During deglaciation, active deposition of an inner levee by turbidity currents, adjacent to an erosional talweg system, recorded in cores from the Younger Dryas (12 ka) to before H1 (16.5 ka). (3) Passive canyon fill during the Holocene by the alongslope Labrador Current, with only minor down-canyon sediment supply. In the active canyon depositional phase, turbidity currents were of variable size, reaching thicknesses >390 m at 40 km down canyon. Numbers of sand beds and mean grain size decrease down canyon, which is inferred to result from rapid entrainment of ambient seawater on the steep gradient and a downflow thinning of the lower part of the current with fine sand in suspension. Silt becomes increasingly segregated from muds downcanyon as a result of floc break-up and re-formation. The processes inferred from Halibut Canyon are representative of other canyons on formerly glaciated margins.

Upper slope processes and seafloor ecosystems on the Sabrina continental slope, East Antarctica

This study applies detailed seafloor bathymetry data and seafloor images to understand upper slope features and how these influence the distribution of seafloor biota on the East Antarctic margin. The East Antarctic slope on the Sabrina margin has been shaped by diverse processes related to repeated glaciation. Differences in the morphology of gullies on the upper slope enable an understanding of the likely processes that have been active on this margin. Gully morphology varies according to changes in slope gradient, which may have driven variations in sedimentation. Areas of lower slope angles may have led to rapid sediment deposition during glacial expansion to the shelf edge, and subsequent sediment failure. Typically, gullies in these areas are U-shaped, initiate well below the shelf break, are relatively straight and long, and have low incision depths, consistent with formation due to mass wastage. Areas of higher slope angles likely experienced enhanced flow of erosive turbidity currents during glaciations associated with the release of sediment-laden basal meltwaters. Sediment-laden subglacial meltwater flows typically create gullies such as those we observe that initiate at, or near, the shelf break; are V-shaped in profile; and have high sinuosity, deep incision depths and a relatively short downslope extent. The short downslope extent reflects a reduced sediment load associated with increased seawater entrainment as the slope becomes more concave in profile. These differences in gully morphology have important habitat implications associated with differences in the composition and beta-diversity of the seafloor communities. This upper slope region also supports seafloor communities that are distinct from those on the adjacent shelf, highlighting the uniqueness of this environment for biodiversity. Conservation strategies therefore need to consider slope and shelf communities as distinct and equally important components of the Antarctic ecosystem.

Bed‐scale spatial patterns in dolomite abundance: Part II. Effect of varied fluid chemistry, flow rate, precursor mineralogy, temperature, textural heterogeneity, nucleation density and bed geometry

AbstractReaction‐transport modelling shows that a lateral, metre‐scale pattern in dolomite abundance can form during replacive dolomitization of calcite and aragonite precursors by Mississippian, Triassic and modern seawaters advecting at >20 cm year−1 in low temperature (≤60°C) hydrogeological systems. The modelled pattern develops best in beds >1 m thick with a relatively uniform nucleate density and a low variance in reactive surface area (for example, grainstones). These conditions suggest that a lateral pattern in dolomite abundance should be expected in dolomites formed by any shallow hydrodynamic system that advects dolomitizing fluid horizontally, including the down‐gradient portion of a reflux system, the oceanward reaches of geothermal (Kohout) convection systems, and the seaward reaches of a seawater entrainment zone below a freshwater aquifer. However, even in those systems, a pattern will not form in all dolomites. Pattern will be muted in thinner (≤ ca 50 cm thick) beds and non‐emergent where the precursor had a high variance in reactive surface area (for example, a skeletal wackestone) and/or large variation in nucleate density. Pattern also did not form at temperatures above ca 60°C, which implies that pattern should not be expected in dolomites formed at intermediate to deep burial depths. As the patterns are horizontal, they also should not be expected where dolomitizing fluids moved vertically (for example, reflux immediately below a brine source). Pattern metrics (short‐range correlation length, and wavelength and amplitude of the longer cyclic component) vary with flow rate, fluid chemistry, bed thickness, porosity, grain size, temperature and the flow complexity (one‐dimensional, two‐dimensional or three‐dimensional) within the bed. However, no modelled pattern produced metrics larger than those documented on dolomite outcrops. The results thus constrain the length scales of porosity and permeability variance to include in petrophysical models of dolomite reservoirs, as well as the geological scenarios in which to consider metre‐scale lateral petrophysical variability.

He–Ar–S Isotopic Compositions of Polymetallic Sulphides from Hydrothermal Vent Fields along the Ultraslow-Spreading Southwest Indian Ridge and Their Geological Implications

Noble gases have become a powerful tool to constrain the origin and evolution of ore-forming fluids in seafloor hydrothermal systems. The aim of this study was to apply these tracers to understand the genesis of newly discovered polymetallic sulphide deposits along the ultraslow-spreading Southwest Indian Ridge (SWIR). The helium, argon, and sulphur isotope compositions of metal sulphide minerals were measured for a number of active/inactive vent fields in the Indian Ocean. The helium concentrations and isotopic ratios in these ore samples are variable (4He: 0.09–2.42 × 10−8 cm3STP∙g−1; 3He: 0.06–3.28 × 10−13 cm3STP∙g−1; 3He/4He: 1.12–9.67 Ra) and generally greater than the modern atmosphere, but significantly lower than those in massive sulphides from the fast-spreading East Pacific Rise (EPR), especially for three Cu–Fe-rich samples from the ultramafic-hosted Tianzuo and Kairei vent fields. On the contrary, most of the SWIR sulphide deposits have somewhat higher 40Ar/36Ar ratios of trapped fluids (ranging from 290.6 to 303.4) when compared to the EPR ore samples. Moreover, the majority of sulphide minerals from the Indian Ocean have much higher δ34S values (3.0‰–9.8‰, ~5.9 on average, n = 49) than other basaltic-hosted active hydrothermal systems on the EPR. Overall, these He–Ar–S results are well within the range of seafloor massive sulphide deposits at global sediment-starved mid-ocean ridges (MORs), lying between those of air-saturated water (ASW) and mid-ocean ridge basalt (MORB) end members. Therefore, our study suggests that the helium was derived mainly from the MORB mantle by degassing during the high-temperature stage of hydrothermal activity, as well as from a mixture of vent fluids with variable amounts of ambient seawater during either earlier or late-stage low-temperature hydrothermal episodes, whereas the argon in ore-forming fluids trapped within sulphide minerals was predominantly derived from deep-sea water. Additionally, relatively high δ34S values exhibit a great estimated proportion (up to nearly 40%) of seawater-derived components. In summary, sub-seafloor extensive fluid circulation, pervasive low-temperature alteration, shallow seawater entrainment, and mixing processes, may make a larger contribution to the SWIR hydrothermal ore-forming systems, compared to fast-spreading centres.

Non-linear response of summertime marine productivity to increased meltwater discharge around Greenland

Runoff from the Greenland Ice Sheet (GrIS) is thought to enhance marine productivity by adding bioessential iron and silicic acid to coastal waters. However, experimental data suggest nitrate is the main summertime growth-limiting resource in regions affected by meltwater around Greenland. While meltwater contains low nitrate concentrations, subglacial discharge plumes from marine-terminating glaciers entrain large quantities of nitrate from deep seawater. Here, we characterize the nitrate fluxes that arise from entrainment of seawater within these plumes using a subglacial discharge plume model. The upwelled flux from 12 marine-terminating glaciers is estimated to be >1000% of the total nitrate flux from GrIS discharge. This plume upwelling effect is highly sensitive to the glacier grounding line depth. For a majority of Greenland’s marine-terminating glaciers nitrate fluxes will diminish as they retreat. This decline occurs even if discharge volume increases, resulting in a negative impact on nitrate availability and thus summertime marine productivity.

Experimental partitioning of Ca isotopes and Sr into anhydrite: Consequences for the cycling of Ca and Sr in subseafloor mid-ocean ridge hydrothermal systems

The elemental and isotopic mass balance of Ca and Sr between seawater and the oceanic crust at mid-ocean ridge (MOR) hydrothermal systems integrates various physiochemical processes in the subseafloor, such as dissolution of primary silicate minerals, formation of secondary minerals, and phase separation in the subseafloor. In particular, the precipitation and recrystallization of anhydrite are recognized as important processes controlling the Ca and Sr elemental and isotope composition of high temperature vent fluids and coexisting ocean crust, and yet, little experimental data exist to constrain the mechanism and magnitude of these critical geochemical effects. Thus, this study experimentally examines Sr/Ca partitioning, Ca isotope fractionation, and the rate of exchange between anhydrite and dissolved constituents. These experimental constraints are then compared with Sr/Ca and Ca isotope compositions of anhydrite and vent fluids sampled from the TAG hydrothermal system. Accordingly, anhydrite precipitation and recrystallization experiments were performed at 175, 250, and 350 °C and 500 bar at chemical conditions characteristic of active MOR hydrothermal systems. Experimental data suggest that upon entrainment and recharge of seawater into MOR hydrothermal systems anhydrite will rapidly precipitate with a Ca isotopic composition that is depleted in the heavy isotope compared to the hydrothermal fluid. The magnitude of the Ca isotope fractionation, Δ44/40Ca(Anh-Fluid), is temperature dependent, −0.45, −0.22, and −0.02‰, for 175, 250, and 350 °C, respectively, but likely indicative of kinetic effects. Utilization of a 43Ca spike in solution was implemented to quantify the time-dependent extent of isotope exchange during anhydrite recrystallization at chemical equilibrium. These data indicate that the rate of exchange is a function of temperature, where 12, 46, and 45% exchange occurred within 1322, 867, 366 h at 175, 250, and 350 °C, respectively. The partitioning of Sr/Ca between anhydrite and constituent dissolved species during precipitation depends greatly on the saturation state of the hydrothermal fluid with respect to anhydrite at each experimental temperature, KD(Anh-Fluid) = 1.24–0.55 at 175–350 °C, broadly similar to results of earlier experimental observations by Shikazono and Holland (1983). Equilibrium KD(Anh-Fluid) values were estimated by taking explicit account of time dependent magnitude of exchange, yielding values of 0.43, 0.36, 0.29 at 175, 250, and 350 °C, respectively. Coupling these experimental constraints with the temperature gradient inferred for high temperature MOR hydrothermal systems suggests that the Ca isotope and Sr elemental composition of anhydrite formed near the seafloor will retain the composition derived upon initial formation conditions, which is indicative of disequilibrium. In contrast, at greater depths and at higher temperatures, anhydrite will reflect close to equilibrium Sr/Ca partitioning and Ca isotope fractionation conditions. The experimental and natural data presented in this study can be used to further understand the effect of anhydrite precipitation during hydrothermal circulation in the oceanic crust and on the chemical and isotopic composition of seawater on geologic timescales.

Progress in Deciphering the Controls on the Geochemistry of Fluids in Seafloor Hydrothermal Systems.

Over the last four decades, more than 500 sites of seafloor hydrothermal venting have been identified in a range of tectonic environments. These vents represent the seafloor manifestation of hydrothermal convection of seawater through the permeable oceanic basement that is driven by a subsurface heat source. Hydrothermal circulation has fundamental effects on the transfer of heat and mass from the lithosphere to the hydrosphere, the composition of seawater, the physical and chemical properties of the oceanic basement, and vent ecosystems at and below the seafloor. In this review, we compare and contrast the vent fluid chemistry from hydrothermal fields in a range of tectonic settings to assess the relative roles of fluid-mineral equilibria, phase separation, magmatic input, seawater entrainment, and sediment cover in producing the observed range of fluid compositions. We focus particularly on hydrothermal activity in those tectonic environments (e.g., mid-ocean ridge detachment faults, back-arc basins, and island arc volcanoes) where significant progress has been made in the last decade in documenting the variations in vent fluid composition.

Measuring fluid flow and heat output in seafloor hydrothermal environments

AbstractWe review techniques for measuring fluid flow and advective heat output from seafloor hydrothermal systems and describe new anemometer and turbine flowmeter devices we have designed, built, calibrated, and tested. These devices allow measuring fluid velocity at high‐ and low‐temperature focused and diffuse discharge sites at oceanic spreading centers. The devices perform at ocean floor depths and black smoker temperatures and can be used to measure flow rates ranging over 2 orders of magnitude. Flow velocity is determined from the rotation rate of the rotor blades or paddle assembly. These devices have an open bearing design that eliminates clogging by particles or chemical precipitates as the fluid passes by the rotors. The devices are compact and lightweight enough for deployment from either an occupied or remotely operated submersible. The measured flow rates can be used in conjunction with vent temperature or geochemical measurements to obtain heat outputs or geochemical fluxes from both vent chimneys and diffuse flow regions. The devices have been tested on 30 Alvin dives on the Juan de Fuca Ridge and 3 Jason dives on the East Pacific Rise (EPR). We measured an anomalously low entrainment coefficient (0.064) and report 104 new measurements over a wide range of discharge temperatures (5°–363°C), velocities (2–199 cm/s), and depths (1517–2511 m). These include the first advective heat output measurements at the High Rise vent field and the first direct fluid flow measurement at Middle Valley. Our data suggest that black smoker heat output at the Main Endeavour vent field may have declined since 1994 and that after the 2005–2006 eruption, the high‐temperature advective flow at the EPR 9°50′N field may have become more channelized, predominately discharging through the Bio 9 structure. We also report 16 measurements on 10 Alvin dives and 2 Jason dives with flow meters that predate devices described in this work and were used in the process of their development. This includes the first advective measurements in the Lau Basin and at the EPR 9°39.5′N. We discuss potential error sources and how they may affect the accuracy of measurements by our devices and other devices. In particular, we use the turbulent plume theory to evaluate the effect of entrainment of ambient seawater.

Quantitative Analysis of Submarine-Flow Deposit Shape In the Marnoso-Arenacea Formation: What Is the Signature of Hindered Settling From Dense Near-Bed Layers?

Abstract Submarine sediment density flows are one of the volumetrically most important processes for sediment transport across Earth. The sediment concentration of flows that reach the deep ocean has never been measured directly, and understanding these long-runout flows remains a major challenge. The Miocene Marnoso-Arenacea Formation in the Italian Apennines is the only ancient sequence where individual submarine sediment-density-flow deposits (single beds) have been mapped out for more than 100 km down-flow. Here we document the external shape and internal architecture of thirty-two individual beds that record flow evolution and can be compared to deposit shapes in mathematical or experimental models. The large number of beds allows modes of flow behavior to be identified. Larger-volume turbidites are typically dominated by massive (TA) or planar-laminated (TB) sandstone intervals that have a broad thickness maximum. This shape is important because it suggests that massive and planar laminated sandstones record hindered settling from dense near-bed layers, which have high (> 10% by volume) sediment concentrations. Previously, some authors have inferred that planar-laminated sandstones (TB) are deposited mainly by dilute flows. The position of the broad thickness maximum moves basinward as the volume of sand in the flow increases. This is consistent with mathematical modeling that suggests the position of the thickness maximum depends on flow thickness, flow speed, and sediment settling velocity, as well as sediment concentration, variations in seawater entrainment rate, and local changes in seafloor gradient. Smaller-volume turbidite sandstone intervals are finer grained and dominated by ripple cross-lamination (TC) and have a near exponential decay in thickness that is consistent with deposition from a dilute sediment suspension. The rate of near exponential thinning is controlled by sandstone volume. In contrast, turbidite mudstone intervals show an approximately linear increase in thickness with distance. Flows that entered the basin in opposite directions produced turbidite mudstone intervals that thicken towards the same location, indicating that muddy turbidity currents can drain back over long distances to basinal lows.

The Effect of Meltwater Plumes on the Melting of a Vertical Glacier Face

AbstractFreshwater produced by the surface melting of ice sheets is commonly discharged into ocean fjords from the bottom of deep fjord-terminating glaciers. The discharge of the freshwater forms upwelling plumes in front of the glacier calving face. This study simulates the meltwater plumes emanated into an unstratified environment using a nonhydrostatic ocean model with an unstructured mesh and subgrid-scale mixing calibrated by comparison to established plume theory. The presence of an ice face reduces the entrainment of seawater into the meltwater plumes, so the plumes remain attached to the ice front, in contrast to previous simple models. Ice melting increases with height above the discharge, also in contrast to some simple models, and the authors speculate that this “overcutting” may contribute to the tendency of icebergs to topple inwards toward the ice face upon calving. The overall melt rate is found to increase with discharge flux only up to a critical value, which depends on the channel size. The melt rate is not a simple function of the subglacial discharge flux, as assumed by many previous studies. For a given discharge flux, the geometry of the plume source also significantly affects the melting, with higher melt rates obtained for a thinner, wider source. In a wider channel, two plumes are emanated near the source and these plumes eventually coalesce. Such merged meltwater plumes ascend faster and increase the maximum melt rate near the center of the channel. The melt rate per unit discharge decreases as the subglacial system becomes more channelized.

Sulfur and oxygen isotope insights into sulfur cycling in shallow-sea hydrothermal vents, Milos, Greece.

Shallow-sea (5 m depth) hydrothermal venting off Milos Island provides an ideal opportunity to target transitions between igneous abiogenic sulfide inputs and biogenic sulfide production during microbial sulfate reduction. Seafloor vent features include large (>1 m2) white patches containing hydrothermal minerals (elemental sulfur and orange/yellow patches of arsenic-sulfides) and cells of sulfur oxidizing and reducing microorganisms. Sulfide-sensitive film deployed in the vent and non-vent sediments captured strong geochemical spatial patterns that varied from advective to diffusive sulfide transport from the subsurface. Despite clear visual evidence for the close association of vent organisms and hydrothermalism, the sulfur and oxygen isotope composition of pore fluids did not permit delineation of a biotic signal separate from an abiotic signal. Hydrogen sulfide (H2S) in the free gas had uniform δ34S values (2.5 ± 0.28‰, n = 4) that were nearly identical to pore water H2S (2.7 ± 0.36‰, n = 21). In pore water sulfate, there were no paired increases in δ34SSO4 and δ18OSO4 as expected of microbial sulfate reduction. Instead, pore water δ34SSO4 values decreased (from approximately 21‰ to 17‰) as temperature increased (up to 97.4°C) across each hydrothermal feature. We interpret the inverse relationship between temperature and δ34SSO4 as a mixing process between oxic seawater and 34S-depleted hydrothermal inputs that are oxidized during seawater entrainment. An isotope mass balance model suggests secondary sulfate from sulfide oxidation provides at least 15% of the bulk sulfate pool. Coincident with this trend in δ34SSO4, the oxygen isotope composition of sulfate tended to be 18O-enriched in low pH (<5), high temperature (>75°C) pore waters. The shift toward high δ18OSO4 is consistent with equilibrium isotope exchange under acidic and high temperature conditions. The source of H2S contained in hydrothermal fluids could not be determined with the present dataset; however, the end-member δ34S value of H2S discharged to the seafloor is consistent with equilibrium isotope exchange with subsurface anhydrite veins at a temperature of ~300°C. Any biological sulfur cycling within these hydrothermal systems is masked by abiotic chemical reactions driven by mixing between low-sulfate, H2S-rich hydrothermal fluids and oxic, sulfate-rich seawater.

Observations of the volume flux of a seafloor hydrothermal plume using an acoustic imaging sonar

We present a 26 day time series (October 2010) of physical properties (volume flux, flow velocity, expansion rate) of a vigorous deep‐sea hydrothermal plume measured using our Cabled Observatory Vent Imaging Sonar (COVIS), which is connected to the Northeast Pacific Time Series Underwater Experiment Canada Cabled Observatory at the Main Endeavour Field on the Juan de Fuca Ridge. COVIS quantitatively monitors the initial buoyant rise of the plume from to above the vents. The time series exhibits temporal variations of the plume vertical volume flux ( ), centerline vertical velocity component ( ) and expansion rate ( ); these variations have major spectral peaks at semidiurnal ( cycle/day) and inertial oscillation ( cycle/day) frequencies. The plume expansion rate (average ) is inversely proportional to the plume centerline vertical velocity component (coefficient of determination ). This inverse proportionality, as well as the semidiurnal frequency, indicates interaction between the plume and ambient ocean currents consistent with an entrainment of ambient seawater that increases with the magnitude of ambient currents. The inertial oscillations observed in the time series provide evidence for the influence of surface storms on the dynamics of hydrothermal plumes.

Uptake of carbon and sulfur during seafloor serpentinization and the effects of subduction metamorphism in Ligurian peridotites

The concentrations and isotope compositions of carbon and sulfur in Ligurian serpentinites having different metamorphic histories were analyzed in order to investigate the behavior of sulfur and carbon during seafloor serpentinization and during subduction metamorphism. Serpentinites associated with gabbros and with seafloor hydrothermal sulfide deposits in northern Apennine ophiolites that exhibit only slight effects of low-grade metamorphism have high sulfur contents (190–1440ppm total sulfur) and δ34STotal S values of up to 9.8‰ through interaction with hydrothermal fluids in high-temperature ultramafic-hosted hydrothermal systems on the seafloor. Fluid circulation was driven by mafic intrusions and the hydrothermal fluids contained a mixture of basaltic and seawater-derived sulfur. The serpentinites contain 250–480ppm total carbon having δ13CTotal C values of −9.4 to −6.0‰, reflecting mixtures of seawater carbonate (~0‰) and reduced (organic) carbon having δ13C≈−25‰ and derived from multiple sources. Entrainment of cold seawater into the subsurface beneath seafloor hydrothermal sulfide deposits maintained locally low temperatures and enabled microbial reduction of seawater sulfate. Combined with previous work documenting low-temperature serpentinization on the seafloor away from such gabbro-driven high-temperature hydrothermal activity, these results provide an integrated view of serpentinization processes in tectonically extended oceanic basement exposed in oceanic core complexes.High-P–T antigorite serpentinites in the Voltri massif (Ligurian Alps) have sulfur and carbon contents and isotope compositions similar to those of the Apennine ophiolites, indicating that the protoliths underwent similar hydrothermal processes on the seafloor. Recrystallization of chrysotile and lizardite to antigorite and minor partial dehydration to olivine during subduction metamorphism result in no significant changes in the contents or isotope compositions of sulfur or carbon in the serpentinites. We estimate that the uptake of carbon and sulfur by serpentinites in oceanic basement is comparable to or greater than that per unit volume of mafic oceanic crust. The high P–T stability of serpentine can, however, make serpentinites important for transport of carbon and sulfur to greater depths in subduction zones.

Geochemistry of hydrothermal fluids from the PACMANUS, Northeast Pual and Vienna Woods hydrothermal fields, Manus Basin, Papua New Guinea

Processes controlling the composition of seafloor hydrothermal fluids in silicic back-arc or near-arc crustal settings remain poorly constrained despite growing evidence for extensive magmatic–hydrothermal activity in such environments. We conducted a survey of vent fluid compositions from two contrasting sites in the Manus back-arc basin, Papua New Guinea, to examine the influence of variations in host rock composition and magmatic inputs (both a function of arc proximity) on hydrothermal fluid chemistry. Fluid samples were collected from felsic-hosted hydrothermal vent fields located on Pual Ridge (PACMANUS and Northeast (NE) Pual) near the active New Britain Arc and a basalt-hosted vent field (Vienna Woods) located farther from the arc on the Manus Spreading Center. Vienna Woods fluids were characterized by relatively uniform endmember temperatures (273–285 °C) and major element compositions, low dissolved CO 2 concentrations (4.4 mmol/kg) and high measured pH (4.2–4.9 at 25 °C). Temperatures and compositions were highly variable at PACMANUS/NE Pual and a large, newly discovered vent area (Fenway) was observed to be vigorously venting boiling (358 °C) fluid. All PACMANUS fluids are characterized by negative δ D H 2 O values, in contrast to positive values at Vienna Woods, suggesting substantial magmatic water input to circulating fluids at Pual Ridge. Low measured pH (25 °C) values (∼2.6–2.7), high endmember CO 2 (up to 274 mmol/kg) and negative δ 34 S H 2 S values (down to −2.7‰) in some vent fluids are also consistent with degassing of acid-volatile species from evolved magma. Dissolved CO 2 at PACMANUS is more enriched in 13C (−4.1‰ to −2.3‰) than Vienna Woods (−5.2‰ to −5.7‰), suggesting a contribution of slab-derived carbon. The mobile elements (e.g. Li, K, Rb, Cs and B) are also greatly enriched in PACMANUS fluids reflecting increased abundances in the crust there relative to the Manus Spreading Center. Variations in alkali and dissolved gas abundances with Cl at PACMANUS and NE Pual suggest that phase separation has affected fluid chemistry despite the low temperatures of many vents. In further contrast to Vienna Woods, substantial modification of PACMANUS/NE Pual fluids has taken place as a result of seawater ingress into the upflow zone. Consistently high measured Mg concentrations as well as trends of increasingly non-conservative SO 4 behavior, decreasing endmember Ca/Cl and Sr/Cl ratios with increased Mg indicate extensive subsurface anhydrite deposition is occurring as a result of subsurface seawater entrainment. Decreased pH and endmember Fe/Mn ratios in higher Mg fluids indicate that the associated mixing/cooling gives rise to sulfide deposition and secondary acidity production. Several low temperature (⩽80 °C) fluids at PACMANUS/NE Pual also show evidence for anhydrite dissolution and water–rock interaction (fixation of B) subsequent to seawater entrainment. Hence, the evolution of fluid compositions at Pual Ridge reflects the cumulative effects of water/rock interaction, admixing and reaction of fluids exsolved from silicic magma, phase separation/segregation and seawater ingress into upflow zones.