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1.
Metal accumulation rates over the East Pacific Rise and Bauer Deep rule out normal authigenic precipitation of iron and manganese as the major mechanism of enrichment to the metalliferous sediments. A hydrothermal source located along the East Pacific Rise is compatible with the transition metal and aluminum accumulation rates. For the Bauer Deep the accumulation rate data suggest either that metal-bearing phases are being transported from the rise to the protected basins of the deep or that a second hydrothermal source exists within the Bauer Deep. A major portion of the minor elements being deposited in the Bauer Deep could result from authigenic precipitation, thus accounting for their distinctive chemical composition.  相似文献   

2.
Based on phosphorus, iron and manganese analyses in 16 cores (5 dated) from the crest and flanks of the East Pacific Rise and the Bauer Deep we estimate that phosphorus is being deposited about 20 times faster in metalliferous sediments near the rise crest than in adjacent flank deposits, and about 40 times faster on the crest than in the Bauer Deep. Almost all of the phosphorus on the rise crest is contained in poorly crystallized hydrothermal iron oxyhydroxides, supporting Berner's (1973) proposal of phosphate sorption by these phases. The phosphate is probably derived from seawater, but some hydrothermal contribution cannot be excluded at this time. Flux estimates indicate that metalliferous sedimentation could remove 15–40% of the pre-agricultural river input of dissolved phosphate.  相似文献   

3.
The ferromanganoan umbers which overlie the uppermost pillow lavas of the Troodos Massif, Cyprus, are strongly enriched in REE relative to normal pelagic clays. Together, the umbers, related ferruginous sediments, and the ochres which are associated with massive cupriferous sulphides located within the lavas, all show light REE enrichment. There is a marked negative Ce anomaly which is characteristic of seawater. Field and chemical data suggest that the REE were incorporated into ferruginous precipitates derived from deep leaching of tholeiitic lavas by seawater. All the metalliferous sediments can be interpreted as related events in the evolution of the Troodos ocean ridge. In contrast, REE patterns of bentonitic clays above the umbers indicate a predominantly continental derivation.  相似文献   

4.
Well-preserved metalliferous sediments and pillow basalts of Lower Ordovician age (ca. 490 Ma) have been studied in an attempt to specify the Nd isotopic composition of Iapetus seawater. Initial143Nd/144Nd ratios of the pillow basalts are indistinguishable from published initial ratios for the 505-Ma Bay of Islands ophiolite complex and are within the anticipated range for MORB-type basalts 500 Ma ago. Metalliferous sediments occur both interstitial to basalt pillows and as well-developed sedimentary accumulations. The initial143Nd/144Nd ratios for the non-interstitial variety range from 0.511851 to 0.511712 (εNd = ?2.7to?5.4) and are considered to provide an estimate of143Nd/144Nd in Iapetus seawater. The interstitial metalliferous sediments show evidence for a significant basalt-derived Nd component. Although volcanic activity occurred at the margin of Iapetus essentially contemporaneous with the formation of the metalliferous sediments, it is clear that arc-type volcanic material was not a major source of Nd in Iapetus seawater. Rather the source of Nd was from continental regions with a similar average age to those supplying material to the present-day Atlantic Ocean.  相似文献   

5.
The distribution of several metals in East Pacific Rise sediments, when normalized to Al2O3, exhibit stronger maxima near the rise crest than when simply plotted on a carbonate-free basis. The similarity (1) between the distribution of metals in ridge sediments and previously measured mean heat flow values and (2) between the composition of crestal sediments and terrestrial ore bodies associated with greenstone belts, strongly supports a hydrothermal origin for rise crest sediments.  相似文献   

6.
Ferromanganoan sediments containing little or no CaCO3 have been found to occur extensively throughout the region between the East Pacific Rise and the Galapagos Rise. Concentrations of Fe and Mn of up to 18 and 6.5%, respectively, accompany low concentrations of Al and Ti. The concentrations of Cu, Ni, and Zn are also high relative to more typical pelagic sediments.While chemically similar to the non-carbonate fraction of metalliferous sediments previously described from the East Pacific Rise, the mineralogy is markedly different. A non-detrital smectite makes up the bulk of sediment (70 to 90%) and is the most important iron bearing phase. Fe and Mn oxides, occurring primarily as micro-nodules, comprise 10 to 20% of the sediment. Detrital material is relatively rare, amounting to less than 10% in all samples.  相似文献   

7.
The Arakapas fault belt, southern Troodos Massif, which is interpreted as a fossil oceanic fracture zone, contains a sedimentary and volcanic “fill” including basaltic lava breccias, volcaniclastic sandstones, intercalated Fe-rich mudstones, and minor Cu sulphide mineralisation. The volcaniclastic sedimentary rocks were produced by submarine weathering and gravity redeposition of basalt within the transform zone. In contrast, the Fe-mudstones predominantly originated as chemical precipitates from hydrothermal solutions generated by hydrothermal leaching of basalt by seawater. The rare earth elements, and some trace metals, including Co, Ni, Pb, V and Zr, are thought to have been incorporated from seawater into the ferruginous precipitates. Unusually high Fe/Mn ratios of the Fe-mudstones relative to most modern ocean-ridge sediments may reflect deposition in relatively oxygen-depleted waters on the floor of a major bathymetric depression created by the transform faulting; release of acidic thermal waters would have further suppressed Mn precipitation. Contrary to recent suggestions of metallogenesis along oceanic fracture zones, none of the major Cyprus cupriferous sulphide bodies lie along the fossil Arakapas transform zone.  相似文献   

8.
A variety of Fe, Mn and trace-metal-enriched Mesozoic pelagic sediments are associated with the tectonically emplaced Antalya Complex in southwestern Turkey. Palaeotectonic settings represented within the complex comprise a continental platform, passing laterally through a Mesozoic passive margin into a zone of marginal oceanic crust, formed during the early stages of continental separation. The origins of the metalliferous sediments are elucidated using mineralogical, major, trace element and REE data, and comparisons with oceanic and ophiolite-related sediments.Late Triassic deposition during the initial continental separation was mostly terrigenous, including detrital carbonate derived from adjacent reef complexes. During the Jurassic and Early Cretaceous the passive margin underwent accumulation of fine-grained terrigenous matter and biogenic silica in deep water below the carbonate compensation depth. Argillaceous mudstones deposited during a regional hiatus at the end of the Upper Triassic show unusual Fe and trace metal enrichment, together with a marked positive Ce anomaly, indicative of slow hydrogenous accumulation.The marginal oceanic crustal zone also shows dominantly terrigenous and siliceous biogenic deposition but with the addition of an important hydrothermal component represented by Fe-Mn deposits. These occur within and immediately above the Upper Triassic lavas of the oceanic crust and as intercalations in the overlying Lower Cretaceous radiolarian chert sequence. Most of these sediments show strong Fe-Mn fractionation; several show a negative Ce anomaly implying rapid incorporation of the REEs from seawater.The Upper Triassic Fe-Mn deposits associated with the lavas are relatively trace-element-depleted and record rapid localised precipitation from relatively high-temperature hydrothermal solutions. By contrast, the more manganiferous and trace-element-enriched metalliferous horizons in the Jurassic to Lower Cretaceous chert sequences represent more dilute low-temperature hydrothermal discharge. Regional comparisons suggest that dominantly manganiferous deposits free of sulphides are characteristic of the early formed Mesozoic ocean crust compared with well established spreading axes like the Troodos Massif, Cyprus.  相似文献   

9.
Under the auspices of the International Decade of Ocean Exploration, scientists from Oregon State University and the Hawaii Institute of Geophysics, along with representatives from the several South American countries which border the Nazca Plate, are intensively studying the origin and economic importance of metalliferous sediments which form extensive deposits on and near the East Pacific Rise. The sediments, enriched in iron, manganese, copper, nickel, zinc, silver, molybdenum, and lead are mineralogically and chemically similar to deposits cored by the “Glomar Challenger”, implying a common origin. The metalliferous sediments are especially abundant in an extensive basin, the Bauer Deep, which occurs about 800 km east of the East Pacific Rise. Elemental and isotopic data, supported by geologic information provided by cores and by geophysical instrumentation, suggest that the enriched elements in the sediments originate by the interplay of volcanism and sea water, by precipitation from sea water alone, and perhaps by the influence of deep-ocean physical processes acting on detritus transported from the continents or from the basaltic East Pacific Rise.An additional objective of the project is to define the possible relationship between marine metalliferous sediments of the plate to ore deposits of the Andean Cordillera. As pointed out by several writers, much of the earth's economic mineralization occurs along zones of convergence between subducted oceanic crust, including metalliferous sediments if present, and continental margins. Field and geochemical techniques are being applied to determine if sediments are in fact subducted beneath the Andean margin, and if they are remobilized into the continental ore deposits of the Andes. Isotopic tracers may prove most useful in testing this relation. Before the model can be tested rigorously, one must know not only the important chemical parameters of the ocean sediment that may be subducted, but also those of the pertinent rock and ore bodies of the South American Cordillera.  相似文献   

10.
87Sr/86Sr ratios of three hydrothermal waters collected on the East Pacific Rise at 21°N define a mixing line between seawater and a hydrothermal end-member at 0.7030 which is derived by seawater-basalt interaction at ca. 350°C and water/rock ratio of about 1.5. Sr concentrations are not affected in the process while Mg uptake from seawater is almost complete. Up to2/3 of this hydrothermal component is involved in anhydrite precipitation while the Sr isotopic ratio in sulfides (chalcopyrite + sphalerite) cannot be distinguished from that of sulfate. It is estimated that ca. 1 × 1010 moles of strontium are yearly cycled in the hydrothermal systems of mid-oceanic ridges, thereby affecting the87Sr/86Sr budget of seawater. Mass balance between river runoff, limestone precipitation and ridge basalt alteration suggests that the87Sr/86Sr ratios of the river runoff are in the range 0.7097–0.7113, and are largely dominated by limestone alteration.  相似文献   

11.
Secular variations in the Pb isotopic composition of a mixed hydrogenous-hydrothermal ferromanganese crust from the Bauer Basin in the eastern Equatorial Pacific provide clear evidence for changes in hydrothermal contributions during the past 7 Myr. The nearby Galapagos Rise spreading center provided a strong hydrothermal flux prior to 6.5 Ma. After 6.5 Ma, the Pb became stepwise more radiogenic and more similar to Equatorial Pacific seawater, reflecting the westward shift of spreading to the presently active East Pacific Rise (EPR). A second, previously unrecognized enhanced hydrothermal period occurred between 4.4 and 2.9 Ma, which reflects either off-axis hydrothermal activity in the Bauer Basin or a late-stage pulse of hydrothermal Pb from the then active, but waning Galapagos Rise spreading center.Hafnium isotope time-series of the same mixed hydrogenous-hydrothermal crust show invariant values over the past 7 Myr. Hafnium isotope ratios, as well as Nd isotope ratios obtained for this crust, are identical to that of hydrogenous Equatorial Pacific deep water crusts and clearly indicate that hydrothermal Hf, similar to Nd, does not travel far from submarine vents. Therefore, we suggest that hydrothermal Hf fluxes do not contribute significantly to the global marine Hf budget.  相似文献   

12.
The hemipelagic mudrocks of the Nankai accretionary prism, Japan, contain hydrothermal deposits associated with a relict spreading center in the Shikoku Basin. Initial work on core samples from Ocean Drilling Program site 808 found several samples with elevated concentrations of calcium, magnesium, iron and manganese, at depths of between 1060 and 1111 m below sea floor. However, the origin of these sediments was uncertain, due to a lack of data. There was no recorded evidence of whether these elevated concentrations were present throughout this interval of core, or if they were present as discrete layers with the background hemipelagic mudrocks in between. In the present study the core was resampled, and the sediments with anomalous chemical compositions were found to be present in discrete layers. This fact, along with a detailed interpretation of their geochemistry, has allowed them to be identified as hydrothermal sediments, associated with the relict spreading center in the Shikoku Basin. The lower (older) two layers display a chemical composition typical of umbers, while the upper (younger) two layers are metalliferous mudrocks typical of deposits found further from the spreading center.  相似文献   

13.
A hydrothermal deposit from explorer ridge in the northeast Pacific Ocean   总被引：1，自引：0，他引：1  
Crusts composed of nontronite and ferromanganese oxides were recovered from Explorer Ridge, a spreading ridge segment in the northeastern Pacific Ocean located off the west coast of Canada. The chemical and mineralogical composition of the crusts closely resembles that of the mound-like hydrothermal deposits recently discovered at the FAMOUS site on the Mid-Atlantic Ridge and on the Galapagos spreading centre. Compositional anomalies suggest that the crusts are precipitates of hydrothermal vent solutions which were ejected discontinuously and subsequently mixed with seawater.  相似文献   

14.
Tholeiitic basalts and sulfide deposits from the “Cyana” and “Alvin” diving programs (RITA project) on the East Pacific Rise were analyzed for Pb and Sr isotopes. The basalt data plot within the field defined previously by other East Pacific Rise basalts (206Pb/204Pb: 18.35–18.58;207Pb/204Pb: 15.48–15.53;208Pb/204Pb: 37.8–38.1;87Sr/86Sr: 0.7022–0.7025). Pb, U and Sr contents (～0.5, ～0.05 and ～110 ppm, respectively) and μ values (～6) are typical of MORB, whereas Th/U ratios (～3.5) are significantly higher.The Pb isotopic ratios of the sulfide samples are very homogeneous (206Pb/204Pb～18.47207Pb/204Pb～15.49208Pb/204Pb～37.90), and plot in the middle of the basalt field. This indicates that (1) the sulfide Pb was derived from the basaltic crust without any significant contribution from either seawater or hemipelagic sediments, and (2) the solutions from which the sulfides were deposited had uniform Pb isotopic composition. The Pb contents of three sulfide samples is relatively high (170–1310 ppm).The Sr contents of five sulfide samples are widely scattered from 12 to 210 ppm, with87Sr/86Sr ratios intermediate between basaltic and seawater values (0.70554±0.00005 to0.70795±0.00011). Leaching experiments show that both basalt-derived Sr and seawater Sr were present in the solutions which deposited the sulfides. In some cases, Sr was also adsorbed from seawater onto the sulfides following their deposition. Basalt-derived Sr and seawater Sr are also present in associated non-sulfide phases.  相似文献   

15.
The interactions of seafloor hydrothermal fluid with igneous rocks can result in leaching elements from the rocks,creating potential ore-forming fluids and influencing the chemical compositions of near-bottom seawater.The hydrothermal alteration of plagioclase microphenocrysts and basaltic glass in the pillow basalts from one dredge station(103°57.62′′W,12°50.55′N,water depth 2480 m)on the East Pacific Rise(EPR)near 13°N were analyzed using a scanning electron microscope(SEM)and energy dispersive X-ray spectrometry(EDS).The results show that the edges of the plagioclase microphenocrysts and the basaltic glass fragments are altered but the pyroxene and olivine microphenocrysts in the interior of the pillow basalts appear to be unaffected by the hydrothermal fluids.In addition,our results show that the chemical alteration at the rims of the plagioclase microphenocrysts and the edges of basaltic glass fragments can be divided into separate types of alteration.The chemical difference in hydrothermal alteration of the plagioclase microphenocrysts and the basaltic glass indicate that different degrees of hydrothermal fluid-solid phase interaction have taken place at the surface of the pillow basalts.If the degree of hydrothermal fluid-solid phase interaction is relatively minor,Si,Al,Ca and Na diffuse from the inside of the solid phase out and as a result these elements have a tendency to accumulate in the edge of the plagioclase microphenocrysts or basaltic glass.If the degree of hydrothermal fluid-solid phase interaction is relatively strong,Si,Al,Ca and Na also diffuse from the inside of solid phase out but these elements will have a relatively low concentration in the edge of the plagioclase microphenocrysts or basaltic glass.Based on the chemical variation observed in the edges of plagioclase microphenocrysts and basaltic glass,we estimate that the content of Si,Al and Fe in the edges of plagioclase microphenocrysts can have a variation of 10.69%,17.59%and 109%,respectively.Similarly,the Si,Al and Fe concentrations in the edges of basaltic glass can have a variation of 9.79%,16.30%and 37.83%,respectively,during the interaction of hydrothermal fluids and seafloor pillow basalt.  相似文献   

16.
Hydrothermal sulfide-sulfate deposits were sampled from eight active and inactive vent sites along the East Pacific Rise at 21°N during the RISE expedition of April, 1979. The mineralogy of the samples has been determined by X-ray diffractometry, scanning electron microscopy, and X-ray energy dispersive analysis. Mounds of Zn, Fe, and Cu sulfides, dominated by sphalerite, pyrite, and lesser chalcopyrite, are topped by inactive and active chimneys, spouting fluids ≤350°C. The outer zones of active chimneys bear abundant anhydrite precipitated from heated ambient seawater, in addition to hydrothermal pyrite and sphalerite. Mg-hydroxysulfate-hydrate, a phase identified in seawater heating experiments, but previously not observed in nature, is intimately intergrown with anhydrite. Hottest chimneys contain massive chalcopyrite±bornite in their interior zones and belch fluids blackened by a presumably non-equilibrium assemblage of pyrrhotite plus minor sphalerite and pyrite. The early, outer walls of chimneys form from sulfates and the sulfide minerals in black smoke, but metastable pyrrhotite in outer zones is rapidly recrystallized to pyrite or marcasite. Reduction in the permeability of the outer walls permits a high-temperature (>～250°C), low-pH environment within chimneys that enhances precipitation of Cu-Fe sulfides in the central zones. Cooler, worm-covered chimneys emit white fluids bearing particulates of amorphous silica, barite, and pyrite. Amorphous silica and barite are also widely associated with fossilized worm-tubes. Two inactive chimneys are filled with sphalerite, wurtzite, sulfur, pyrite, and marcasite. Anhydrite has been dissolved from these dead chimneys, and the sulfate assemblage is dominated by barite and alteration products such as jarosite and natrojarosite. Silicates other than amorphous silica are not abundant in these deposits, although talc forms in hot chimneys from seawater Mg and hydrothermal silica, and nontronite is found in sediments on the crest of the East Pacific Rise. Other accessory phases identified include copper-rich sulfides such as cubanite, chalcocite, covellite, and digenite; galena; Fe-oxyhydroxides, including goethite; and gypsum. Chimney debris accumulates to form basal mounds, and the mineralogical differences between mounds and chimneys are attributable to weathering of mounds. Mn-oxyhydroxides form crusts within a few meters of the vents, but are not coprecipitating with the sulfide/sulfate minerals.  相似文献   

17.
The mineralogy of five groups of hydrothermal chimneys from the East Pacific Rise has been examined. Three of the chimneys, where the exit temperature of the hydrothermal fluids was close to 350°C, are rich in copper sulfides. Exit temperatures from the other two chimneys were less than 300°C; in these, the chimney walls are rich in zinc sulfide. The major sulfides in the chimneys as a whole were found to be wurtzite, chalcopyrite, pyrite, and cubanite. Anhydrite is always the dominant sulfate, and is present in all the deposits. Silicates are also present but in relatively minor amounts. There are considerable differences in the mineralogy of sulfides, sulfates, and silicates between the active and inactive vent deposits.The isotopic composition of sulfur in anhydrites from active vents is close to that of seawater; the δ34S values of the sulfides range from +1.3 to +4.1‰. The isotopic composition of sulfur in the anhydrites is consistent with a derivation predominantly from seawater sulfate. The sulfur in the sulfides must have a complex origin including contributions from both sulfur in basalts and sulfide produced by reduction of sulfate in seawater. Mixing of H2S-dominated hydrothermal fluids with cold seawater near the seafloor resulted in the precipitation of non-equilibrium assemblages of sulfides and sulfates.  相似文献   

18.
The mineralogical and geochemical characteristics of Fe-oxyhydroxide samples from one dredge station (long. 103°54.48′W, lat. 12°42.30′N, water depth 2655 m) on the East Pacific Rise near lat 13°N were analyzed by XRD, ICP-AES, and ICP-MS. Most Fe-oxyhydroxides are amorphous, with a few sphalerite microlites. In comparison with Fe-oxyhydroxides from other fields, the variable ranges in the chemical composition of Fe-oxyhydroxide samples are very narrow; their Fe, Si, and Mn contents were 39.90%, 8.92%, and 1.59%, respectively; they have high Cu (0.88%–1.85%) and Co (65×10−6−704×10−6) contents, and contain Co+Cu+Zn+Ni> 1.01%. The trace-element (As, Co, Ni, Cu, Zn, Ba, Sr) and major-element (Fe, Ca, Al, Mg) contents of these samples are in the range of hydrothermal sulfide from the East Pacific Rise near 13°N, reflecting that this type of Fe-oxyhydroxide constitutes a secondary oxidation product of hydrothermal sulfide. The Fe-oxyhydroxide samples from one dredge station on the East Pacific Rise near 13°N are lower in ΣREE (5.44×10−6–17.01×10−6), with a distinct negative Ce anomaly (0.12–0.28). The Fe-oxyhydroxide samples have similar chondrite-normalized rare-earth-element (REE) patterns to that of seawater, and they are very different from the REE composition characteristics of hydrothermal plume particles and hydrothermal fluids, showing that the REEs of Fe-oxyhydroxide are a major constituent of seawater and that the Fe-oxyhydroxides can become a sink of REE from seawater. The quick settling of hydrothermal plume particles resulted in the lower REE content and higher Mn content of these Fe-oxyhydroxides, which are captured in part of the V and P from seawater by adsorption. The Fe-oxyhydroxides from one dredge station on the East Pacific Rise near 13°N were formed by secondary oxidation in a low temperature, oxygenated environment. In comparison with the elemental (Zn, Cd, Pb, Fe, Co, Cu) average content of hydrothermal sulfide samples from the East Pacific Rise near 13°N, the Zn, Cd, and Pb contents of the Fe-oxyhydroxides are lower, and their Fe, Co, and Cu contents are higher. Supported in part by the Pilot Project of Knowledge Innovation Project, Chinese Academy of Sciences (Grant No. KZCX3-SW-223), and the Special Foundation for the Tenth Five Plan of COMRA (Grant No. DY105-01-03-1)  相似文献   

19.
The flux of226Ra from bottom sediments has been determined from patterns of226Ra/230Th disequilibrium in ten deep-sea cores from the world oceans. Values range from ? 0.0015 dpm/cm2 yr (in the Atlantic) to 0.21 dpm/cm2 yr (in the north equatorial Pacific). The flux is poorly related to sediment type, but is inversely correlated in a non-linear fashion with sediment accumulation rate. There is a direct relationship between the production rate of226Ra near the sediment-water interface (i.e. the integrated230Th activity in the biologically mixed zone) and the226Ra flux. The226Ra concentration in near-bottom water follows the geographic variation in the226Ra flux. The high flux from north equatorial Pacific sediments especially is reflected in the high bottom water226Ra concentrations in that area. The data suggest that both rate of circulation and the magnitude of the radium flux influence the near-bottom226Ra concentration.  相似文献   

20.
Easter and Sala y Gomez Islands lie along the Sala y Gomez Ridge, a broad zone of high topography and scattered seamounts extending east-southeast from the East Pacific Rise. K-Ar ages and major element abundances of volcanic rocks from these islands are used to test the fixed melting spot hypothesis for the origin of this feature. Poike volcano, the oldest center on Easter Island, was constructed in two episodes, occurring at 2.5 and 0.9 m.y. ago. Eruptive activity on Sala y Gomez was nearly contemporaneous with the earliest volcanism on Easter Island. No migration of volcanism with time is apparent along the Sala y Gomez Ridge. Basaltic rocks from Easter Island have tholeiitic affinities, while those dredged from the base of Sala y Gomez belong to an alkali olivine basalt series. Differences in basalt chemistry suggest that the volcanic rocks from the two islands formed from magmas that equilibrated at different pressures, and a model is presented which relates the character of the erupted liquids to magma segregation at the base of a progressively thickening lithosphere. The islands and seamounts comprising the Sala y Gomez Ridge do not fall on a small circle about the Nazca-mantle pole of absolute motion. Available evidence, therefore, does not support a fixed melting spot origin for Easter Island, Sala y Gomez, and the Sala y Gomez Ridge. Rather, it appears that the Sala y Gomez Ridge formed along a leaky fracture zone, and in response to a major re-orientation of spreading centers in this area.  相似文献   

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