Hydrothermal manganese oxide deposits from Baby Bare seamount in the Northeast Pacific Ocean     

《Marine Geology》2006,225(1-4):145-156

Manganese oxide crusts were recovered from Baby Bare seamount in order to investigate the history of off-axis hydrothermal venting. Baby Bare is a small basement high protruding from a regional sediment cover on the eastern flank of the Juan de Fuca Ridge that acts as a focus for discharging crustal fluids. Stratabound Mn-oxide crusts were collected where warm venting has been observed near the seamount summit. Mn-oxide crusts are composed primarily of 10 Å manganate ± pyrolusite, with minor nontronite, saponite, and/or barite. These assemblage and chemical characteristics such as high Mn/Fe ratios and low trace metal and REE concentrations are indicative of a hydrothermal origin. Minimum ages for these deposits, calculated using growth rates (324 to ∼ 1800 mm/Ma) and estimated thicknesses of manganese outcrops, show that Baby Bare has been hydrothermally active for at least 0.5 Myr, and possibly since its formation (1.7–2.7 Ma). Hydrothermal manganese oxide crusts such as these from Baby Bare record interactions between the hydrothermal fluids and seawater and are important tools for estimating the longevity of off-axis hydrothermal activity.  相似文献   

Comparative mineralogy and geochemistry of hydrothermal iron‐rich crusts from the Pitcairn,Teahitia‐mehetia,and Macdonald hot spot areas of the S. W. pacific     

P. Stoffers  G. P. Glasby  D. Stuben  R. M. Renner  T. G. Pierre  J. Webb 《Marine Georesources & Geotechnology》2013,31(1):45-86

Abstract

Hydrothermal iron‐rich crusts have been recovered from a number of hot spot volcanos including Crough Seamount, Pitcairn Volcanos 2 and 1, Cyana Seamount, Teahitia, Moua Pihaa, and Macdonald Seamount in the S. W. Pacific. Mineralogically, the crusts consists of ferrihydrite with traces of the weathering products of volcanic ash (feldspar, nontronite, pyroxene, and serpentinite). The iron oxyhydroxide phase has a mean particle size of 3–4 nm indicating rapid deposition. Electron microprobe studies have revealed the presence of filamentous iron‐silica deposits within the crusts reflecting the possible bacterial oxidation of iron from the hydrothermal fluids. The crusts display wide variability in composition both between individual sampling stations and between seamounts. Endmember analysis shows that the compositional data can be resolved into three endmembers: a Fe‐rich endmember, a light and heavy rare earth element endmember, and a Ba (barite)‐rich endmember. The Fe‐rich endmember appears to contain very low concentrations of most trace elements. For bulk samples, the composition of the iron‐rich crusts reflects dilution of the iron oxyhydroxide phase by volcanic ash and, to a lesser extent, a hydrogenous component. This is illustrated by the wide variability in SiO₂ (11.1–71.3%) and Mn (0.01–1.21%) contents of the crusts. For iron‐rich crusts containing greater than 40% Fe, the Pitcairn crusts display lower contents of Pb, Ba, Mo, U, Th, As, and rare earth elements (REE) and lower cerium anomalies than those from Teahitia. REE profiles of crusts from each of the hot spot volcanoes are characterized by small negative cerium anomalies but pronounced positive europium anomalies. The low average La/Fe ratios of the crusts from the various seamounts (47–572 X 10^‐6) and positive Eu anomalies of the crusts suggest rapid deposition of the iron oxyhydroxide near the hydrothermal vent. The high Fe/Mn ratio of vent fluids at hot spot volcanoes (8.5–5.6) may account for the formation of these iron‐rich crusts. The present data indicate that there may be differences in the nature of the iron‐rich crusts based on the depth of occurrence. This influences the temperature of the venting hydrothermal fluids and the possibility of occurrence of submarine phreatomagmatic eruptions.  相似文献   

Submersible observations of manganese nodule and crust deposits on the Tenpo Seamount,Northwestern Pacific     

Akira Usui  Akira Nishimura  Kokichi Iizasa 《Marine Georesources & Geotechnology》2013,31(4):263-291

Pavements of manganese nodules and crusts and outcrops of Miocene limestones were observed on the flanks and flat top of the Tenpo Seamount during three Shinkai 2000 dives. The pre‐Miocene volcano supplied nuclei of volcanic rocks and hydrothermal manganese deposits, and subsequent slow or no sedimentation promoted deposition of abundant hydrogenetic nodules and crusts, mainly on the upper flank of the seamount. Nodule pavements generally cover calcareous sand surface sediments, while crusts cover hard outcrops composed probably of volcanic rocks. The fields of crusts and nodules are sparsely distributed with each other on scales of meters to tens of meters. The on‐site observation suggests the deposits have encountered tectonic and/or mass movements that resulted in unusual occurrences of densely stacked nodules and occasionally the nodules resting directly on crusts or hard substrates. Mineralogical and chemical compositions reveal that for nodules and crusts the encrusting manganese layers of around 1 cm thickness are composed of hydrogenetic vernadite, and diagenetic influence is negligible.  相似文献   

Direct barite determination using SEM/EDS-ACC system: implication for constraining barium carriers and barite preservation in marine sediments     

E. Robin  C. Rabouille  G. Martinez  I. Lefevre  J. L. Reyss  P. van Beek  C. Jeandel 《Marine Chemistry》2003,82(3-4):289-306

Barite (BaSO₄) in marine sediments is considered as a proxy of surface ocean productivity and is widely used for paleo-productivity reconstructions. However, direct barite determination is not achieved by currently used methods, which rely on the measurement of total barium by inductively coupled plasma–mass spectrometry (ICP-MS) and instrumental neutron activation analysis (INAA) and correction from the allogenic Ba contribution. We report here on a technique that directly counts individual barite crystals using a scanning electron microscope (SEM) coupled to an energy dispersive spectrometer (EDS) equipped with an automated particle counting and classification (ACC) system. We show that barite–Ba concentrations can be deduced from the abundance, shape and size distributions of barite crystals with current precision and sensitivity as high as ±5 wt.% (2σ confidence limit) and 10 ppm, respectively. This technique, coupled with ICP-MS and INAA techniques for total Ba measurements, was applied to sediment samples from the tropical North Atlantic and the Central North Pacific oceans. Results show that: (1) barite and detrital aluminosilicates are the two main carriers of Ba in the investigated sediments; (2) calculated Ba/Al ratios range from 0.005 to 0.008 with an average value around 0.0066, in close agreement with previously reported values; (3) barite might not be the major source for released barium out of sediments and we suggest instead adsorbed barium as a potential source.  相似文献   

Modes of sapropel formation in the eastern Mediterranean: some constraints based on pyrite properties     

《Marine Geology》1999,153(1-4):199-219

Pyrite formation within and directly below sapropels in the eastern Mediterranean was governed by the relative rates of sulphide production and Fe liberation and supply to the organic-rich layers. At times of relatively high SO²⁻₄ reduction, sulphide could diffuse downward from the sapropel and formed pyrite in underlying sediments. The sources of Fe for pyrite formation comprised detrital Fe and diagenetically liberated Fe(II) from sapropel-underlying sediments. In organic-rich sapropels, input of Fe from the water column via Fe sulphide formation in the water may have been important as well. Rapid pyrite formation at high saturation levels resulted in the formation of framboidal pyrite within the sapropels, whereas below the sapropels slow euhedral pyrite formation at low saturation levels occurred. δ³⁴S values of pyrite are −33‰ to −50‰. Below the sapropels δ³⁴S is lower than within the sapropels, as a result of increased sulphide re-oxidation at times of relatively high sulphide production and concentration when sulphide could escape from the sediment. The percentage of initially formed sulphide that was re-oxidized was estimated from organic carbon fluxes and burial efficiencies in the sediment. It ranges from 34% to 80%, varying significantly between sapropels. Increased palaeoproductivity as well as enhanced preservation contributed to magnified accumulation of organic matter in sapropels.  相似文献   

Origin and distribution of hydrogen sulfide in the Yuanba gas field,Sichuan Basin,Southwest China     

《Marine and Petroleum Geology》2016

The Yuanba gas field in the Permian Changxing Formation (P₂c), which exhibits wide variations in its hydrogen sulfide (H₂S) concentration (1.20–12.16%), is a typical sour gas field in the northern Sichuan Basin. The sulfur-rich reservoir's solid bitumen (atomic S/C ratios are 0.032–0.142), and late calcite cement δ¹³C values, which are smaller than the δ¹³C values of the host dolostone, indicate that the H₂S originated from thermal sulfate reduction (TSR) and oil was involved in TSR. The gas souring index (GSI) of P₂c's gases is generally lower than 0.1. The ethane δ¹³C values increase as the GSI increases, although no obvious increase was observed in the methane δ¹³C values. The calcite cements' δ¹³C values (−15.36 to +4.56‰) in dolostone are heavier than the typical reported values, which implies that only limited heavy hydrocarbon gases were involved in TSR. No anhydrites developed in P₂c's reservoirs, and dissolved sulfate anions (SO₄²⁻) were mainly enriched during dolomitization. Insufficient dissolved SO₄²⁻ most likely caused the lower H₂S concentrations in the Permian to Triassic reservoirs in the northeastern Sichuan Basin compared to the Permian Khuff Formation in Saudi Arabia and the Jurassic Smackover Formation in Mississippi. Except for the SO₄²⁻ in residual water in paleo-oil zones, SO₄²⁻ from bottom water may also be involved in TSR; therefore, oil reservoirs with bottom water have more SO₄²⁻ and can produce more H₂S than pure oil reservoirs. This phenomenon may be the main cause of the great difference in the H₂S concentrations between reservoirs, while gravitational differentiation during late uplift most likely creates differences in H₂S concentrations in a single reservoir. Carbon dioxide (CO₂), which has a relatively heavy δ¹³C value (−3.9 to −0.3‰), may be the combined result of TSR, the balance between CO₂ and inorganic fluid systems, and carbonate decomposition.  相似文献   

天然气水合物赋存区甲烷渗漏活动的地球化学响应特征     

程俊  王淑红  黄怡  颜文 《海洋科学》2019,43(5):110-122

综述了天然气水合物赋存区甲烷渗漏活动的地球化学响应指标的研究进展,分析了应用单一指标识别甲烷渗漏活动各自所存在的问题,包括浅表层沉积物孔隙水中CH_4、SO_4~(2–)、Cl~–等离子浓度随深度的变化;浅层沉积物全岩W_(TOC)(W表示质量分数,TOC表示总有机碳)和W_(TS)(TS表示总硫)之间的相关性及比值;自生碳酸盐岩δ~(13)C和δ~(18)O;自生矿物重晶石、黄铁矿、自生石膏的δ~(34)S;有孔虫壳体和生物标志化合物的δ~(13)C等。结果表明孔隙水中的CH_4、SO4_~(2–)浓度及溶解无机碳的碳同位素组成可以用来识别目前正在发生的甲烷渗漏活动;而沉积物中的WTS、自生矿物的δ~(34)S、钡含量及其异常峰值和生物标志化合物的δ~(13)C等指标的联合使用可以更真实准确地反映地质历史时期天然气水合物赋存区的甲烷渗漏活动。因此,在实际研究过程中,可将孔隙水和沉积物两种介质的多种指标相结合。随着非传统稳定同位素(Fe、Ca、Mg等)和沉积物氧化还原敏感元素(Mo、V、U等)等研究的发展,甲烷渗漏活动地球化学响应指标的研究也将得到拓展,而多种地球化学指标的联合使用将为天然气水合物勘探及其形成分解过程识别研究提供重要的科学依据。  相似文献   

Sulfate reduction and anaerobic methane oxidation in Black Sea sediments     

《Deep Sea Research Part I: Oceanographic Research Papers》2001,48(9):2097-2120

Beyond the shelf break at ca. 150 m water depth, sulfate reduction is the only important process of organic matter oxidation in Black Sea sediments from the surface down to the sulfate–methane transition at 2–4 m depth. Sulfate reduction rates were measured experimentally with ³⁵SO₄²⁻, and the rates were compared with results of two diffusion-reaction models. The results showed that, even in these non-bioirrigated sediments without sulfide reoxidation, modeling strongly underestimated the high reduction rates near the sediment surface. A hybrid modeling approach, in which experimentally measured rates in the upper sediment layers force a model that includes also the deeper layers, probably provides the most realistic estimate of sulfate reduction rates. Areal rates of sulfate reduction were 0.65–1.43 mmol SO₄²⁻ m⁻² d⁻¹, highest in sediments just below the chemocline. Anaerobic methane oxidation accounted for 7–11% of the total sulfate reduction in slope and deep-sea sediments. Although this methane-driven sulfate reduction shaped the entire sulfate gradient, it was only equivalent to the sulfate reduction in the uppermost 1.5 cm of surface sediment. Methane oxidation was complete, yet the process was very sluggish with turnover times of methane within the sulfate–methane transition zone of 20 yr or more.  相似文献   

Minor and rare elements in manganese crusts and nodules and sediments from the Manihiki plateau and adjacent areas: Results of HMNZS Tui cruises     

H. Kunzendorf  G. P. Glasby 《Marine Georesources & Geotechnology》2013,31(4):271-281

Six manganese crusts, 13 manganese nodules, and 16 sediments were analyzed by instrumental neutron activation analysis. Data were generated on selected major and minor elements but geochemical evaluations are based only on Fe, Sc, U, Th, and the rare earth elements (REE). Manganese crusts and manganese nodules have comparable trivalent REE contents and show a shale‐like distribution pattern. Both crusts and nodules are characterized by a positive Ce anomaly but the anomaly is higher in nodules. REE contents in manganese nodules show a linear dependence on the Fe content, and it is concluded that these elements are incorporated in the Fe‐rich (δ‐MnO₂) phase. In the crusts, the REE correlate with Sc and are therefore assumed to be associated with the clay minerals. Uranium contents are significantly higher in the crusts than in nodules whereas Th is slightly higher in the nodules. There is a clear positive correlation between U and Th in nodules but there are too few data to make a similar conclusion for crusts. Compositional data suggest a division of the sediments into two groups. The carbonate sediments have much lower REE contents and a more pronounced negative Ce anomaly than the clays, while both show a lithogenous component as indicated by a slight negative Eu anomaly.  相似文献   

Dissolved nutrient fluxes from the nearshore sediments of Bowling Green Bay,central Great Barrier Reef Lagoon (Australia)     

《Estuarine, Coastal and Shelf Science》1987,24(3):289-303

The fluxes of dissolved inorganic N, P, and Si from the nearshore sediments of the Great Barrier Reef Lagoon are significantly lower than those reported from sediments in temperate regions at similar temperatures. The directly measured fluxes range from −23 to +28, −154 to +890, and −990 to +1750 μmol m⁻² day⁻¹ for PO₄³⁻, ΣN(=NH₄⁺ + NO₂⁻ + NO₃⁻) and Si, respectively. Estimates suggest that sediments are the major source of dissolved N to near-shore waters of the Lagoon greatly exceeding the dissolved flux from rivers. Resuspension of up to 1 cm of sediment during storms would have a very small effect on the PO₄³⁻ or Si(OH)₄ concentration of the overlying water, but would significantly raise the ΣN concentration. The productivity of these waters may be controlled at various times by the balance between the steady-state sedimentary flux of nutrients, the fluvial input, and storm resuspension.  相似文献   

Composition and secondary alterations of microfossils in sediments of the Ashadze-1 hydrothermal field (tropical Mid-Atlantic Ridge)     

I. F. Gablina  L. L. Demina  O. B. Dmitrenko  N. S. Os’kina  E. A. Popova  T. A. Khusid  V. V. Shilov 《Oceanology》2011,51(3):476-490

The first thorough analysis of microfossils from ore-bearing sediments of the Ashadze-1 hydrothermal field in the Mid-Atlantic Ridge sampled during cruise 26 of the R/V Professor Logachev in 2005 revealed the substantial influence of hydrothermal processes on the preservation of planktonic calcareous organisms, as well as on the preservation and composition of the benthic foraminifers. From the lateral and vertical distribution patterns and the secondary alterations of the microfossils, it is inferred that the main phase of the hydrothermal mineralization occurred in the Holocene. Heavy metals (Cu, Co, Cr, and Ag) were accumulated by foraminiferal tests and in their enveloping Fe-Mn crusts. The distribution of authigenic minerals replacing foraminiferal tests demonstrates local zoning related to the hydrothermal activity. There are three mineral-geochemical zones defined: the sulfide zone, the zone with an elevated Mg content, and zone of Fe-Mn crusts.  相似文献   

Mineralogy and composition of manganese crusts and nodules and sediments from the Manihiki plateau and adjacent areas: Results of HMNZS Tui Cruises     

P. Walter  G. P. Glasby  W. L. Plüger  H. Kunzendorf  M. A. Meylan 《Marine Georesources & Geotechnology》2013,31(3):321-337

Forty‐four sediment samples and 23 Mn crusts and Mn nodules have been analyzed for several elements in order to characterize their geochemical nature. Most of the Mn crusts and Mn nodules are of hydrogenous origin, although one crust (U375) from the flanks of the Rarotonga volcano is thought to be of hydrothermal origin. δ‐MnO₂ is the principal Mn mineral in the crusts, whereas todorokite and birnessite occur in addition to δ‐MnO₂ in the nodules. The sediments can be divided into carbonates, with calcite as the dominant phase, and deep‐sea clay, consisting mainly of illite and smectite.  相似文献   

Submarine hydrothermal brine seeps off Milos, Greece. Observations and geochemistry     

M. f. Fitzsimons  P. R. Dando  J. A. Hughes  F. Thiermann  I. Akoumianaki  S. M. Pratt 《Marine Chemistry》1997,57(3-4)

A shallow hydrothermal brine seep located off the Greek island of Milos in the Aegean Sea was studied. The brine fluid outcropped as a pool of water in a seabed depression and was detected in the surrounding pore-waters of sediments colonised by the sulphur bacterium Achromatium volutans. The seep fluid was highly saline and sulphidic, depleted in Mg²⁺ and SO₄²⁻, but enriched over seawater in Na⁺, Ca²⁺, K⁺, Cl⁻, SiO₂, reduced species and dissolved gases. The high concentrations of Na⁺, Ca²⁺ and K⁺ were consistent with the Milos tectonic setting. Na-K and Na-K-Ca geothermometers predicted a reservoir temperature of 300–325 °C for the most concentrated seep samples. The deep geothermal reservoir within the metamorphic basement of Milos island has already been located and studied and may represent the source of the seep fluid. Faunal diversity was lowest in seep-influenced sediments, but a sulphide-intolerant species was found in areas of the bacterial mat where salinity and temperature were much lower. Pressure-induced variations in the vertical depth of the brine interface may be occurring in the sediment.  相似文献   

Uptake of selenium and other oxyanionic elements in marine ferromanganese concretions of different origins     

Noburu Takematsu  Yoshio Sato  Shiro Okabe  Akira Usui 《Marine Chemistry》1990,31(1-3)

The concentration of selenium in marine ferromanganese concretions varies between 0.02 and 1.2 mg kg⁻¹, with an average of 0.6 mg kg⁻¹. This is about two orders of magnitude lower than previously reported. In contrast to minor cationic elements, the concentrations of selenium are relatively uniform between ferromanganese concretions of different origins, except for hydrothermal crusts. It shows the same trends of element enrichment as other oxyanionic elements. The incorporation of selenium into ferromanganese concretions is attributed to adsorption of selenate on iron and manganese oxides.  相似文献   

Deposition of hydrogenetic and hydrothermal manganese minerals in the Ogasawara (Bonin) Arc Area,Northwest Pacific     

Akira Usui  Shigeru Terashima 《Marine Georesources & Geotechnology》2013,31(2):127-154

A widespread distribution of hydrothermal and hydrogenetic manganese deposits is described in the results of the Hakurei‐Maru cruises conducted in the Bonin Arc areas of the West Pacific from 1984 to 1989. Manganese deposits occur in the active volcano chains, back‐arc basins, remnant back‐arc ridges, and oceanic seamounts.

The hydrogenetic iron‐manganese deposits commonly form earthly black crusts and nodules on the topographic highs of inactive ridges and old seamounts, sometimes as thick as 10 cm. They are always composed of the iron‐manganese mineral vernadite. Co and Ni contents are relatively high in the crusts from the seamounts in the open Pacific Ocean (up to 1.1% Co and 1.0% Ni). Two generations of distinct chemistry and texture are typical of these crusts, which can be compared to reported thick crusts from the Central Pacific seamounts.

The hydrothermal deposits, characterized by dense, submetallic, and gray appearance, are dominant in the recent and also in past submarine volcanoes of the island‐arc systems. Evidence of past hydrothermal activity was ascertained as fossil hydrothermal manganese deposits inside the hydrogenetic nodules or beneath the hydrogenetic crusts over the Tertiary island arc. Their component minerals are considered to be todorokite and bimessite (stable and contractible upon dehydration), having almost negligible amounts of Fe, Si, Al, Ni, Co, Zn, Pb, Cu, etc. In the small model site, the Kaikata Seamount hydrothermal area, the presumably recent hydrothermal activity has yielded thin slabs of pure manganate deposits growing downward within volcanic and sand layers.

Early diagenetic influence is negligible on nodules of this area.  相似文献   

Effects of oxic and anoxic filtration on determined methyl mercury concentrations in sediment pore waters     

《Marine Chemistry》2007,103(1-2):76-83

Accurate determination of methyl mercury (MeHg) concentrations in sediment pore waters is crucial for an improved understanding of mercury (Hg) biogeochemistry, and for improved risk assessment of Hg contaminated sites. In the present study, effects of oxic (air) and anoxic (N₂) filtration (after centrifugation) on determined pore water MeHg concentrations were investigated in severely Hg contaminated pulp fibre sediments from two estuaries of the Bothnian Sea, Sweden. MeHg was determined in the filtrate using species-specific isotope dilution gas chromatography inductively coupled plasma mass spectrometry (SSID–GC–ICPMS), after ethylation with sodium tetraethylborate. Determined concentrations of MeHg were greater after anoxic filtration than after oxic filtration for all samples investigated, with MeHg(N₂)/MeHg(air) ratios ranging between 3.4 and 343. Adsorption to newly formed Fe(III)/Mn(III/IV)-oxy/hydroxide surfaces is proposed as the main mechanism responsible for MeHg removal during oxic filtration. This is supported by decreases in dissolved Fe and Mn concentrations during oxic filtration, and by decreases in dissolved sulphur concentrations during oxic filtration in the samples with largest effect on MeHg concentrations. The latter is explained by adsorption of SO₄²⁻ to newly formed Fe(III)/Mn(III/IV)-oxy/hydroxide surfaces. The effect of oxidation during filtration on pore water MeHg concentrations was largest in samples in which FeS(s) was not present, but with calculated pe-values below − 3. Thus, our results indicate that the largest errors with respect to pore water MeHg concentrations when filtering in air can be expected in samples with an intermediate redox potential, possibly buffered by a mixture of oxidation sensitive Fe(II/III) minerals.  相似文献   

Chemical and isotopic evidence for the nature of the fluid in CH4-containing sediments of the Håkon Mosby Mud Volcano     

A. Lein  P. Vogt  K. Crane  A. Egorov  M. Ivanov 《Geo-Marine Letters》1999,19(1-2):76-83

The pore waters of CH₄-containing sediments of the Håkon Mosby Mud Volcano were rich in NH⁺ ₄, Br^-, and I^-; exhibited a high total alkalinity; but were poor in Cl^-and SO^2- ₄. The geological evidence and our data suggest that organic matter decomposition in preglacial or early interglacial sediments took place during early diagenesis (bacterial processes) and during metamorphism (thermogenic processes under the 3100-m-thick layer of glacial sediments), accompanied by mud volcano fluid generation. It is argued that the CH₄of the mud volcano sediments has a mixed, biogenic and thermogenic, origin.  相似文献   

Mineralogical and geochemical constraints on the origin of ferromanganese crusts from the Rivera Plate (western margin of Mexico)     

Carles Canet  Rosa María Prol-Ledesma  William L. Bandy  Peter Schaaf  Carlos Linares  Antoni Camprubí  Esperana Tauler  Carlos Mortera-Gutirrez 《Marine Geology》2008,251(1-2):47-59

Marine hydrogenetically precipitated ferromanganese crusts are widespread in the Pacific Ocean. They occur as pavements coating volcanic or sedimentary hard-rock substrates, mainly on the slopes of seamounts, plateaus and hills in ocean basins and continental margins. We studied three ferromanganese crusts from one dredge haul from the Rivera Plate (western margin of Mexico), which are up to 15 mm thick and grow directly on a substrate of pillow basalt fragments. They consist of laminated, botryoidal, porous aggregates mostly of Fe and Mn oxyhydroxides and up to 10% silicates. XRD analysis showed the predominance of poorly crystallized mineral phases in the crusts that include Mn-feroxyhyte and vernadite, and an authigenic smectite-like clay. Detrital minerals probably derive from granodiorites of the eastern wall of the neighboring Middle America Trench. Scattered barite grains occur on the crust surface and suggest plume fall-out derived from hydrothermal vents, although a possible pelagic source cannot be dismissed. Ratios between major (Fe, Mn, Si) and trace (Co, Ni, Cu) elements reveal that such crusts are predominantly hydrogenetic in origin, although they show a hydrothermal influence that increases in the outer layers. Iron contents range from 16.2 to 25.2 wt.%, and manganese from 3.4 to 14.5 wt.%. The Fe/Mn ratio ranges from 1.6 to 7.0. The SiO₂/Al₂O₃ ratio ranges from 4.3 to 6.6, indicating the presence of biogenic silica (radiolarians). The concentrations of copper (up to 383 ppm) and cobalt (up to 534 ppm) are significantly below those of the typical hydrogenetic crusts, whereas Ni (up to 1320 ppm) is about the same or slightly lower. REE normalized profiles and ΣREE values (486 to 732 ppm) match those reported for hydrogenetic crusts, but suggest a hydrothermal contribution for the later crust layers. The inferred crust growth rates using the Co-chronometer (44 and 229 mm/Myr) are higher than those reported for pure hydrogenetic crusts (mostly 1 to 6 mm/Myr), thus indicating an increasing hydrothermal influence. The highest growth rate (229 mm/Myr, corresponding to the outer crust layers) suggests a regional hydrothermal input of iron and manganese to seawater. The intensification of regional submarine hydrothermal activity began about 13,000 yr ago, and may be related to the tectonic activity in the complex junction of the Rivera, Cocos, Pacific and North America plates.  相似文献   

Mineral-forming and diagenetic processes related to Tertiary hydrocarbon seepage at the Bohemian Massif/Outer Western Carpathians interface: Evidence from the Hrabůvka quarry,Moravia, Czech Republic     

《Marine and Petroleum Geology》2014

Ancient hydrocarbon seepage occurred in the Hrabůvka quarry at the boundary between the basement of the Bohemian Massif (represented by folded Lower Carboniferous siliciclastics of the Culm facies) and Tertiary sedimentary cover of the Carpathian Foredeep (formed by Lower Badenian siliciclastics and calcareous clays). The unconsolidated Lower Badenian sediments contain lithified domains composed of limestone and breccias with limestone cement, whereas the basement rocks are cut by subvertical neptunic dykes filled up by limestone and calcite-marcasite-pyrite veinlets representing sealed fluid conduits. The deeply negative δ¹³C values of both vein calcite and limestone (down to −38.1‰ V-PDB) indicate that oxidation of hydrocarbons was the major source of carbon for authigenic mineralization. A fluid inclusion study suggests low fluid temperatures (<50 °C) and low and variable salinities of aqueous fluids associated with hydrocarbons (0.7–6.7 wt. % NaCl eq.). The variability of δ¹⁸O values of authigenic carbonates (−1.7 to −8.2‰ V-PDB) could reflect either slight changes in temperature of escaping fluids (mostly within 15 °C), and/or some mixing with meteoric waters. The low δ³⁴S values of vein marcasite (∼–20‰ V-CDT) are consistent with bacterial reduction of sulfate in the hydrothermal system. Low C₁/(C₂+C₃) ratios in hydrocarbon gas extracted from authigenic carbonates (9.9 and 5.8) as well as the high δ¹³C values of methane (−31.8 and −32.4‰ V-PDB) are compatible with a thermogenic source of hydrocarbons. REE data indicate sequestration of REE from finely dispersed detrital material in the apical part of the hydrothermal system. The available data are compatible with two possible scenarios of fluid origin. The hydrocarbons could have been leached from underlying Paleozoic sedimentary sequence by aqueous fluids that infiltrated into the basement after Tertiary tectonic reactivation. Alternatively, an external source of hydrocarbon-bearing fluids can be found in the adjacent Outer Western Carpathians flysch nappes containing petroleum-producing lithologies. Nevertheless, a regional flow of hydrocarbon-bearing fluids is evidenced by the occurrence of very similar hydrocarbon-bearing vein mineralizations in a wider area.  相似文献   

Spatial variation in shallow sediment methane sources and cycling on the Alaskan Beaufort Sea Shelf/Slope     

《Marine and Petroleum Geology》2013

The MITAS (Methane in the Arctic Shelf/Slope) expedition was conducted during September, 2009 onboard the U.S. Coast Guard Cutter (USCGC) Polar Sea (WAGB-11), on the Alaskan Shelf/Slope of the Beaufort Sea. Expedition goals were to investigate spatial variations in methane source(s), vertical methane flux in shallow sediments (<10 mbsf), and methane contributions to shallow sediment carbon cycling. Three nearshore to offshore transects were conducted across the slope at locations approximately 200 km apart in water column depths from 20 to 2100 m. Shallow sediments were collected by piston cores and vibracores and samples were analyzed for sediment headspace methane (CH₄), porewater sulfate (SO₄²⁻), chloride (Cl⁻), and dissolved inorganic carbon (DIC) concentrations, and CH₄ and DIC stable carbon isotope ratios (δ¹³C). Downward SO₄²⁻ diffusion rates estimated from sediment porewater SO₄²⁻ profiles were between −15.4 and −154.8 mmol m⁻² a⁻¹ and imply a large spatial variation in vertical CH₄ flux between transects in the study region. Lowest inferred CH₄ fluxes were estimated along the easternmost transect. Higher inferred CH₄ flux rates were observed in the western transects. Sediment headspace ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ values ranged from −138 to −48‰, suggesting strong differences in shallow sediment CH₄ cycling within and among sample locations. Measured porewater DIC concentrations ranged from 2.53 mM to 79.39 mM with δ¹³C_DIC values ranging from −36.4‰ to 5.1‰. Higher down-core DIC concentrations were observed to occur with lower δ¹³C where an increase in ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ was measured, indicating locations with active anaerobic oxidation of methane. Shallow core CH₄ production was inferred at the two western most transects (i.e. Thetis Island and Halkett) through observations of low ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ coupled with elevated DIC concentrations. At the easternmost Hammerhead transect and offshore locations, ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ and DIC concentrations were not coupled suggesting less rapid methane cycling. Results from the MITAS expedition represent one of the most comprehensive studies of methane source(s) and vertical methane flux in shallow sediments of the U.S. Alaskan Beaufort Shelf to date and show geospatially variable sediment methane flux that is highly influenced by the local geophysical environment.  相似文献