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1.
We propose that the precipitation of a gelatinous iron-sulphide membrane is the necessary first step towards life. Membrane vesicles were inflated with alkaline, sulphide-bearing hydrothermal (<200°C) solution and grew on a submarine sulphide mound in acid iron-bearing Hadean seawater. Once a critical size had been reached (0.1–1 mm) vesicles would have budded contiguous self-similar daughters. We assume that the membrane was rendered insulating by the adsorption and/or oxidative precipitation of organic and organosulphur compounds. As a consequence of the naturally induced proton-motive (chemiosmotic) force, and the activity of the iron monosulphide redox catalysts within the membrane, organic compounds would have accumulated within the vesicle. Osmotically driven growth therefore became more significant with time. The geochemical environment envisaged as responsible for this first step towards life is consistent with that widely accepted for the early Earth. 相似文献
2.
Michael J. Russell 《Ore Geology Reviews》1996,10(3-6)
Notwithstanding the current fashion which favours an epigenetic origin for what used to be termed SEDEX deposits, there are several lines of evidence to indicate that Phanerozoic base-metal orebodies of this type have at least some exhalative aspects. The fossil polychaete worms, which occur in Lower Carboniferous pyrite mounds at Tynagh and Silvermines in Ireland, have affinities to Paralvinella, an organism that lives attached to hydrothermal chimneys at the Juan de Fuca hot spring site in the Northeast Pacific. In addition, fossil tube worms, and their moulds, occur both in silica masses underlying the Carboniferous giant Red Dog sulphide orebody in Alaska and in Devonian barite and base-metal deposits in North America and in Russia, respectively. The development of sulphide and carbonate fossil microbialites over exhalative centres further supports generation of some mineral deposits on sea or lake floors. Carbonate microbialite mounds are also developing today over warm springs and seepages.The existence of an environment in which sulphide mineralisation developed at the sea floor has implications also in a different sphere. Life itself may have emerged in a similar milieu at 4.2 Ga from iron monosulphide bubbles. A primitive metabolism could have been driven by the high, long-lived and constant, redox potential of 300 mV made available across an iron monosulphide membrane which would have been spontaneously generated where sulphide-bearing, submarine, alkaline springs issued into the acidic, iron-bearing, Hadean ocean. The alkaline spring provided bisulphide to the iron-rich (carbonic) acid ocean for the precipitation of iron-monosulphide bubbles (probotryoids), as well as acetate (Shock, 1992) — the feeder to the biochemical Krebs cycle, driven in reverse by the high partial pressure of CO2. In addition to its scientific significance, an understanding of these beginnings may well benefit research into many aspects of economic geology.Even more extreme redox contrasts are revealed by the presence of sedimentary jasper or iron formation in three of the major Carboniferous sulphide orebodies in Ireland. Pyritic sulphide microbialites also grew over some of the associated fossil hot-spring sites and may be recognised by their bacteriogenic δ34S values (−20 to −40‰). Recognition of such fossil hot-spring sites could lead to further discoveries of SEDEX deposits. 相似文献
3.
ZHANG Qiling HOU Zengqian TANG ShaohuaInstitute of Mineral Deposits Chinese Academy of Geological Sciences Baiwanzhuang Ro Beijing 《《地质学报》英文版》2001,75(2):196-203
A preliminary organic geochemical study shows that the sulphide ores from the hydrothermal deposit of the Okinawa Trough are generally low in the total organic carbon and extremely low in the soluble organic matter. In the aliphatic hydrocarbon fraction, the n-alkanes range from C15 to C35, with usual maxima in the middle n-C20 region and strong odd-carbon number predominance when n > C25 (CPI = 1.2). The dominant analog in the aromatic fraction is phenanthrene, a polynuclear aromatic hydrocarbon, which provides evidence for hydrothermal activity. The organic matter derived mainly from marine planktonic and terrigenous vascular plants is entrapped in a high-temperature regime such as an active chimney and cooled quickly in the sulphide ores on the seafloor. Organic matter and sulphides are definitely products of a high-temperature alteration. The biomarker compounds indicate that the ores are formed under low Eh and pH conditions-a reducing to anoxic environment, which is favourable for sulphates to be 相似文献
4.
E.M Cameron 《Geochimica et cosmochimica acta》1983,47(6):1069-1074
Seven units of carbonaceous shale or sulphide-facies iron-formation have been sampled. They are associated with Proterozoic iron-formations that range in age from ~ 1.9 to ~2.5 Ga: Sokoman and Gunflint (Canada), Riverton (United States), Penge (South Africa) and Brockman (Australia). Sulphur isotope ratios have been determined on the sulphides removed from these shales by both physical and chemical means.The mean δ34S composition of the seven units varies between ?4.9%. and +6.6%. and the sample variance is low within each unit. These distributions are more characteristic of hydrothermal sulphide than sulphide produced by biogenic reduction. This hydrothermal sulphide is believed to have originated from high temperature reduction of seawater sulphate and from magmatic sulphide. A model is suggested whereby this sulphide was exhaled into stratified anoxic/oxic basins. The sulphide and associated base metals were deposited in the reduced sediments beneath the anoxic waters, while some iron and manganese was deposited on oxygenated shelves.The data support, but do not prove, a hydrothermal exhalative origin for lower Proterozoic iron-formation. 相似文献
5.
K. G. McQueen 《Mineralium Deposita》1989,24(2):100-110
Geochemically anomalous, pyritic sediments occur directly above a Mid Silurian unconformity in the Quidong area of southeastern New South Wales. The composition of these sediments reflects derivation from a mixture of: (a) feldspar- and mica-depleted detritus reworked from underlying quartz-rich flysch; (b) Mg-rich clay or chlorite precipitated from hydrothermal exhalations; and (c) pyrite formed by reaction of iron in clays or oxides with reduced sulphur derived largely from sea-water sulphate and possibly a magmatic source. Three types of base metal sulphide mineralisation occur at Quidong including: (a) weak syngenetic concentrations in the pyritic sediments; (b) stratabound and fault-controlled bodies of massive sulphides hosted by the pyritic sediments and containing higher grade Pb, Zn and Cu; and (c) small vein and cavity fillings of galena, barite and other minor sulphides in overlying limestones. All types of mineralisation are related to hydrothermal activity which occurred during and after deposition of the pyritic facies. The geochemistry of the immediately underlying basement rocks and Pb isotope data indicate that the source of the metal-bearing fluids was deeper in the crust and probably related to widespread partial melting and magmatic processes. The sulphidic sediments and stratabound sulphide deposits represent syngenetic-epigenetic, sediment hosted mineralisation developed in a shallow marine environment, distal from major volcanic centers. This style of mineralisation has not previously been described from the region. It has some similarities to the Irish-Alpine type spectrum of deposits best known in Europe. 相似文献
6.
Transient release of Ni,Mn and Fe from mixed metal sulphides under oxidising and reducing conditions
C. Naylor W. Davison M. Motelica-Heino L. M. van der Heijdt G. A. van den Berg 《Environmental Earth Sciences》2012,65(7):2139-2146
The potential release of metals from anoxic sediments exposed to oxygen was investigated by using a synthetic preparation
of metal sulphides dominated by solid phase FeS. The technique of DGT (diffusive gradients in thin-films) was used to measure
sulphide and Fe, Mn and Ni in the anoxic metal-sulphide slurry, which had a pH of 6.4. Speciation calculations based on these
data showed there was moderate supersaturation with respect to amorphous FeS in the solution phase. Measurements made using
DGT with a range of diffusion layer thicknesses showed that when Fe, Mn and Ni are removed from solution there is fairly rapid
(minutes) release from the solid phase, that is reasonably well sustained. This presumed desorptive release will be responsible
for elevated concentrations of some metals in solution when sediments are resuspended. Oxidation of the slurry by bubbling
with air rapidly (hours) removed Fe, Mn and Ni from the pore water solution. While Fe concentrations in solution remained
low after the removal, Mn and Ni were transiently released. These results were consistent with initial rapid oxidation of
Fe(II) to oxyhydroxides, which remove Mn(II) and Ni by adsorption. The slower oxidation of FeS then releases Mn and Ni, but
these too are eventually removed by adsorption to iron oxyhydroxides. These data suggest that oxidation of metal sulphides
will contribute to the release of metals from sediment disturbed by dredging or remedial aeration, but it is likely to be
short lived, with complete removal within a day. 相似文献
7.
Various Fe–S minerals of the mackinawite–greigite–pyrite association, ubiquitous in biogenic remains from Jurassic mudstones, have been described in detail in an SEM–EDS study. Two diagenetic stages of Fe sulphide formation and preservation in the Jurassic organic skeletons are identified. In the first stage, pyrite formed as euhedra and framboids shortly after deposition, mainly in the interiors of the skeletons which still contained labile organic matter. The second stage of iron sulphide formation was related to the later stages of diagenesis, when the influence of the surrounding sediment was more dominant, although some organic matter was still present in the biogenic skeletons. A Fe-rich carbonate–aluminosilicate cement was then introduced between the earliest iron sulphides and later subsequently sulphidized, to form a metastable iron monosulphide of mackinawite composition and then greigite. 相似文献
8.
Felix Bilek 《Environmental Geology》2006,49(5):674-683
Dump groundwaters in the former East-German lignite-mining district are characterized by high amounts of ferrous iron and
sulphate. Both the pyrite weathering products endanger the surface water quality when discharged into lakes. Only the precipitation
of both contaminants in the subsurface can prevent the further contamination of surface waters. The two-step process of microbial
catalyzed sulphate reduction and iron sulphide precipitation is limited by the low availability of natural organic substances
as electron donators. Therefore, a new remediation technique is developed based on the injection of a liquid organic electron
donator (methanol) into the contaminated aquifer. The saturated aquifer is used as a bioreactor, where iron monosulphides
are precipitated in the groundwater-filled pore space. Column experiments were performed under natural pressure and temperature
conditions with natural anoxic groundwater and original sediments to test the remediation technology. The test showed that
a complete iron removal (4 mmol/l), even under rather acid conditions (pH 3.8), is possible after having established an active
sulphate reducer population. The turnover of the added organic substance with sulphate is complete and the amount of the resulting
sulphide controls the effluent pH. In addition, intensified microbial activity triggers the turnover of natural organic substances.
Also, natural Fe(III) hydroxides react with the sulphide produced. Considering the long natural retention times (decades),
artificially enhanced FeS precipitation is spontaneous, although it shows kinetic behaviour in the range of days. In light
of the promising results, the development of a field scale application of this technique is considered to be necessary. It
will have to focus on the improved precipitation control of the FeS in the subsurface. 相似文献
9.
海底黑烟囱的识别研究及其科学意义 总被引：22，自引：4，他引：18
现代海底黑烟囱广泛出现于大洋中脊、弧后盆地、浅海及大陆裂谷等环境,形成巨大规模的块状硫化物,并且在黑烟囱周围发现了化学自养细菌。海底硫化物黑烟囱具有明显的柱状-锥状构造形态,常保留通道构造,矿物同心圈状分带明显。黑烟囱的形成涉及热液流体与海水相互作用,外壁快速沉淀及通道内部硫化物结晶等过程。深部岩浆热源、热液沿裂隙集中流动和持续喷发,有利于形成大规模黑烟囱构造。海底硫化物丘体的钻探及其与地史时期块状硫化物的对比研究表明,它们具有相似的内部构造和矿床分带特征。黑烟囱的生长、垮塌以及丘体内部角砾化、交代、重结晶作用,有助于大规模矿床的形成。最后,在块状硫化物中寻找黑烟囱残片的研究,对于探讨成矿过程与早期生命活动具有重要意义。 相似文献
10.
Diagenesis of metal-organic complexes in sediments: Formation of metal sulphides from cystine complexes 总被引：1，自引：0，他引：1
J.D. Saxby 《Chemical Geology》1973,12(4):241-248
Metal-cystine complexes of iron, lead, zinc, copper and nickel under mild artificial diagenesis give rise to crystalline metal sulphides and insoluble organic matter as well as gaseous and “oily” organic products. Under confined reducing conditions at 200°C for 100 h a virtual 100% conversion of metal complex to metal sulphide occurs, while < 10% of the associated organic material may remain as kerogen. Such a mechanism could account for the formation of metal sulphides and in particular pyrite from protein- or amino acid-rich material in carbonaceous sediments during diagenesis. 相似文献
11.
David Rickard 《Chemical Geology》1989,78(3-4):315-324
The first precipitate formed through the reaction between aqueous Fe(II) salts and dissolved sulphide at ambient temperatures and pH < 9, appears to be a highly disordered gel approaching the composition Fe(HS)2 on a water-free basis. After 0.4 s this precipitate loses sulphide and amorphous FeS begins to appear. The mackinawite structure begins to develop after several hours.
The rate of formation of the initial precipitate can be approximated by a pseudo first-order reaction, directly dependent on total sulphide concentration and with an apparent pseudo first-order rate constant of 48 ± 9 s−1. Dissolved Fe concentration does not appear to be rate limiting.
The estimated solubility of the initial phase is variable but consistently one to two orders of magnitude greater than the measured solubilities for amorphous FeS. In natural systems this may lead to variable Fe(II) solubilities in sulphidic environments. This initial material may play a more central role in iron sulphide reaction pathways than either mackinawite or amorphous FeS. 相似文献
12.
PU Chuanjie QIN Dexian NIAN Hong ZHANG Xueshu Franco PIRAJNO FAN Zhuguo 《中国地球化学学报》2007,26(4):374-383
The sulphide ores of the Baimazhai deposit, although typically orthomagmatic, locally exhibit peculiar textural features and are intimately associated with hydrothermal minerals, such as biotite, amphibole and chlorite. This association suggests that the magmatic sulphide ores were subjected to hydrothermal alteration and subsequent redistribution, resulting in the observed textural features. Geochemically, the Baimazhai sulphide ores are enriched in Cu, Pd and Au, which,according to previous studies, reflects the action of hydrothermal fluids. Interestingly, Ar-Ar dating yielded the plateau ages of about 160–170 Ma, which are at odds with the established Permian age of the Emeishan large igneous province. We interpreted these younger ages as due to thermal resetting during post-Permian tectonothermal events. We have proposed a model in which tectonic movements and hydrothermal fluids related to these events modified the pre-existing magmatic sulphides. Given the degree of overprint, we suggested two possible scenarios: 1) the sulphide disseminations that surround the massive magmatic ores are the result of deformation and hydrothermal alteration; and 2) there were both magmatic massive and disseminated sulphides, in which case the scale and relocation of remobilization would have been smaller, but still detectable. 相似文献
13.
Since lenses of chert are common within the volcano-sedimentary succession hosting the massive sulphide deposits of the Iberian Pyrite Belt (Spain and Portugal), we examined numerous chert occurrences, both petrographically and geochemically, to test their possible value for massive sulphide exploration. The chert is found at two main lithostratigraphic levels (upper and lower) that are also interpreted as massive-sulphide bearing. In both cases the chert is located at the top of acidic volcanic sequences or in the associated sediments; we have not been able to observe the relationships between massive sulphides and chert, but some of the large orebodies of the Province (Lousal, La Zarza, Tharsis, Planes-San Antonio body of Rio Tinto, Neves) are described as being locally capped by chert facies. Four main types are recognized among the chert and associated facies: (1) red hematitic chert?±?magnetite; (2) radiolarian and/or sedimentary-textured (conglomeratic) chert with hematite and/or Mn oxides; (3) pale sulphidic chert; (4) rhodonite and/or Mn carbonate?±?magnetite facies. In the Spanish part of the Province the radiolarian chert is confined to the upper level; the distribution of the other types appears to be haphazard. The hydrothermal origin of the South Iberian chert is shown by its high Fe-Mn and low Co-Ni-Cu contents. The presence of small positive Ce anomalies indicates a shallow marine environment (shelf or epicontinental sea), which is consistent with the volcanological and sedimentological data. The chert was emplaced below the sea floor through chemical precipitation and/or through alteration and replacement of the country rock, residual traces of which are ghost phenocrysts and high Al, Ti and rare earth contents. Macro- and microscopic relationships indicate that the oxide facies (hematite?±?magnetite) formed first, probably providing a protective insulating cover against the marine environment and enabling an evolution towards sulphide facies; a phase of Mn?carbonate and silicate + quartz?±?chlorite + sulphides appears to be even later. It was not possible, through discrimination, to isolate a chert that could be considered as representing a lateral marker of massive sulphides; moreover, both field observations and geochemical data seem to indicate a relative independence of this siliceous sulphide hydrothermal activity from the hydrothermal activity giving rise to the massive sulphides. Such is also indicated by the lead isotopic signature of the chert, which is appreciably more radiogenic than that of the massive sulphides; the lead enrichment in the sulphidic chert facies indicates the participation of a different source (sediments, sea water) from that of the massive sulphides. The hypothesis of an independent hydrothermal “chert” event can thus be envisaged, wherein the chert reflects submarine low-temperature hydrothermal activity that is most apparent during a “break” within the volcano-sedimentary succession and which may locally have competed with the high-temperature hydrothermal activity giving rise to the massive sulphides. The interest of the chert thus rests in its palaeodynamic significance, as a marker of periods of volcanic quiescence, and in its possible role as a protective insulating cap favourable to the deposition of massive sulphides. 相似文献
14.
15.
The Filón Norte orebody (Tharsis, Iberian Pyrite Belt) is one of the largest pyrite-rich massive sulphide deposits of the world. The present structure of the mineralization consists of an internally complex low-angle north-dipping thrust system of Variscan age. There are three major tectonic units separated by thick fault zones, each unit with its own lithologic and hydrothermal features. They are internally organized in a hinterland dipping duplex sequence with high-angle horses of competent rocks (igneous and detritic rocks and massive sulphides) bounded by phyllonites. The mineralization is within the Lower Unit and is composed of several stacked sheets of massive sulphides and shales hosting a stockwork zone with no obvious zonation. The Intermediate Unit is made up of pervasively ankeritized shales and basalts (spilites). Here, hydrothermal breccias are abundant. The Upper Unit is the less hydrothermally altered one and consists of silicified dacites and a diabase sill. The tectonic reconstruction suggests that the sequence is inverted and the altered igneous rocks were originally below the orebody. Carbon, oxygen and sulphur isotopes in the massive sulphides and hydrothermal rocks as well as the mineral assemblage and the paragenetic succession suggest that the sulphide precipitation in the sea floor took place at a low temperature (<≈150?°C) without indication, at least in the exposed section, of a high-temperature copper-rich event. Sporadic deep subsea-floor boiling is probably responsible for the formation of hydrothermal breccias and the wide extension of the stockwork. Its Co-Au enrichment is interpreted as being related with the superposition of some critical factors, such as the relationship with black shales, the low temperature of formation and the boiling of hydrothermal fluids. The present configuration and thickness of the orebody is due to the tectonic stacking of a thin and extensive blanket (2–4?km2) of massive sulphides with low aspect ratio. They were formed by poorly focused venting of hot modified seawater equilibrated with underlying rocks into the seafloor. Massive sulphide precipitation took place by hydrothermal fluid quenching, bacteriogenic activity and particle settling in an unusual, restricted, euxinic and shallow basin (brine pool?) with a low detritic input but with important hydrothermal activity related to synsedimentary extensional faulting. Resedimentation of sulphides seems to be of major importance and responsible for the observed well-mixed proximal and distal facies. The tectonic deformation is largely heterogeneous and has been mostly channelled along the phyllonitic (tectonized shales) deformation bands. Thus, sedimentary and diagenetic textures are relatively well-preserved outside the deformation bands. In the massive sulphides, superimposed Variscan recrystallization is not very important and only some early textures are replaced by metamorphic/tectonic ones. The stockwork is much more deformed than the massive sulphides. The deformation has a critical effect on the present morphology of the orebody and the distribution of the ore minerals. This deposit is a typical example of the sheet-like, shale-hosted, anoxic, low temperature and Zn-rich massive sulphides developed in a ensialic extensional basin. 相似文献
16.
J.M. Edmond 《Journal of Geochemical Exploration》1983,19(1-3)
Hydrothermal fields on submarine spreading centres were first studied systematically during dives of the deep submersible ALVIN on the crest of the Galapagos Ridge in 86°W in the spring of 1977. While the exiting waters had temperatures only about 20°C above that of the ambient water column detailed analysis of their chemistry showed them to be formed by mixing of cold sea water (as “ground-water”) with a hydrothermal endmember of approximate temperature 350°C. Subsequently fields of hot springs with this temperature were found on the crest of the East Pacific Rise at 21°N by ALVIN in 2 600 metres water depth. Reconnaissance water sampling of these systems was made in November 1979 and a detailed study has just been completed (November 1981).The 350°C solutions are completely depleted of their original sea-water concentrations of Mg and SO4. They are acid with a pH (25°C, 1 atmos) of 3.6 and an acidity of 400 μeq/kg. They contain about 7 mmol/kg of H2S. The isotopic composition of this sulphur and the arsenic to sulphur ratio in the solutions indicate that about 85% of it is of igneous origin. The “soluble elements” Li, K and Rb are strongly enriched over the sea-water values, as are Ca and Ba. Sr is present at close to the sea-water concentrations however the isotopic compositon is identical to that of the basalts. The exiting solutions are clear and homogeneous super-critical fluids of in situ density approximately 0.65 g/cm3. Velocities in the throat of the orifices are around 1.5 m/sec. The iron concentrations are 1.8 mmol/kg and the Fe/Mn ratio is about 3. The reconnaissance samples gave Zn of 120 μol/kg and Cu and Ni of about 15 μol/kg.Upon mixing with sea-water the hot springs precipitate a voluminous black “smoke” predominantly composed of fine-grained FeS. Anhydrite is precipitated around the throat of the orifice producing chimney-like constructional features up to 10-m high. As these grow vertically the anydrite is replaced by sulphide minerals. The outer surface of the chimneys is colonized by several species of worms that secrete mats of tubes, up to several centimetres in diameter, composed of a tough organic material. Lateral growth of the chimneys via leaks in their walls leads to precipitation of sulphide minerals in a morphology controlled by the organic mats. All the numerous extinct sulphide deposits in the area have this characteristic surface texture.The active deposits on the EPR are unlike ophiolite type massive sulphides chemically, mineralogically and texturally. However, they do represent the primary precipitate. It appears that during lateral growth and coalescence of the chimneys in a given field the original deposit is reworked chemically as the 350°C solutions stream through the disequilibrium rapidly precipitated material. A “zone refined” substrate results consisting of coarsely crystalline, permeable relatively pure pyrite. This secondary deposit is, of course, capped with juvenile chimneys. It is these that probably constitute the ochres, the oxidized surficial zones of massive sulphides historically worked for silver and other elements present at only trace levels in the bulk deposit. 相似文献
17.
Proximal brecciform ferruginous and manganiferous rocks related to VMS deposits of the Urals are subdivided into jasperites, gossanites, and umbers, in addition to thin-bedded jaspers and cherts. The coherence of host rock composition and Mn–Fe-fertility of the sediments have been established. Fe-poor pink hematitic and gray sulphidic chert are typical of the felsic class of VMS deposits. In contrast the contents of Fe vary from high to moderate in ferruginous rocks enclosed in basaltic units associate with VMS deposits. Fe- and Mn-rich ferruginous rocks and umbers occur in association with limestones and calcareous sedimentary rocks in both types of volcanic sequences. A common feature of jasperites and umbers is the abundance of replacement textures of hyaloclastites and carbonates by hematite and silica. In addition, replacement of clastic sulphides by hematite and magnetite is a characteristic genetic feature of gossanites. All of these sedimentary rocks are accompanied by pseudomorphs of hematite and quartz formed after bacterial filaments. The abundance of replacement textures are supportive of the halmyrolysis model, in addition to hydrothermal sedimentary and sub-seafloor hydrothermal replacement theories. Study of chemical zonation of altered hyaloclasts shows depletion of their rims, not only in mobile Na, K, Mg, but also in immobile Al, Ti, and REE; whereas Si and Fe are concentrated in situ. The halmyrolysis model presented here, involving organic-rich calcareous hyaloclastic sediments, resolves the problem of subtraction of Al, Ti, REE and other elements, which are commonly immobile under hydrothermal conditions. The evolution of the halmyrolysis process from acidic reducing to alkaline oxidized conditions infers a possible range in transformation from FeII–Mg smectites to Fe-silicates and Fe-Si oxides as precursors of brecciform jasperite and thin-bedded jasper. The higher acidic, initial stage, of gossanite formation seems to be required for oxidation of organic matter and/or pyrite. The acidic condition facilitates the temporal preservation of “immobile” elements (Al, Ti, REE) in “immature”chlorite–hematite gossanites. Another peculiarity of the gossanite-forming processes is the likely sorption of P, U and V by iron hydroxides displacing sulphides. The general evolution of all ferruginous sediments results in complete Fe2+ oxidation and silicification accompanied by subtraction of other elements. The vertical diagenetic differentiation leads to concentration of Mn-carbonates, silicates and oxyhydroxides into the tops of jasperite and gossanite layers. Mn oxyhydroxides scavenge positively charged hydrated cations like Co and Ni. Near-vent bacterial communities may activate the processes of volcanic glass and sulphide degradation. The proposed processes of halmyrolysis followed by silicification, in situ, may resolve the enigma of silica-rich sediment formation in a silica undersaturated ocean. The discrimination between gossanite and jasperite is useful for elaboration of new criteria for local exploration of VMS- and Mn-deposits. Halo dispersion of gossanites covering an area about two to three times that of the massive sulphide deposit is a good vector for ore body discovery. Proximal gossanites can be differentiated from jasperites by presence of relic sulphide clasts or elevated contents of chalcophile elements (Cu, Fe, Zn, Pb, Bi, Te, As, Sb, Ba), noble metals (Au, Ag) and distinct REE patterns with La and Eu positive anomalies. The development of halmyrolysis and biomineralization models merit further elaboration and testing in on-going research, in order to add or revise theories of iron and manganese deposit formation. 相似文献
18.
Concentrations of iron sulphide minerals in sediments within and adjacent to a small intertidal thermal pool near Talasea township are forming and being modified under a wide range of exhalative-sedimentary conditions. A geochemical, mineralogical and bacteriological investigation of these iron sulphides has defined the major reactions leading to their formation and indicated aspects in which their mineralogies, textures and mechanisms of formation differ significantly from those of iron sulphides formed under “normal” sedimentary conditions. The main features of the thermal pool environment are: 1. the occurrence of relatively high iron sulphide concentrations; 2. the preservation, by the strongly anaerobic thermal spring waters, of hydrotroilite formed in the thermal pool sediments in the presence of excess sulphide; 3. the presence in the pool banks of major marcasite (which appears to replace its dimorph pyrite) formed as a result of the development of strongly acidic conditions; 4. the abundance in the pool banks of large euhedral crystals of pyrite and marcasite, and the scarcity of framboids; 5. the presence of sulphate-reducing bacteria in the thermal waters and sediments. 相似文献
19.
Heavy mineral separates of peat from a mineralotrophic bog contain sulphide minerals with distinctive textures. Pyrite framboids, consisting of spherical aggregates of subhedral pyrite crystals, are surrounded by a thin rim of chalcopyrite or a layer of massive marcasite. Clusters of framboids are cemented by covellite which also occurs as small idiomorphic grains, with rectangular or hexagonal outlines, surrounded by chalcopyrite. The sulphides appear to have resulted from discharge of groundwaters, enriched in copper from weathering of primary sulphides in bedrock and in iron by reduction of the till underlying the peat, into the hydrogen sulphide charged bog. 相似文献
20.
S. Oszczepalski 《Mineralium Deposita》1999,34(5-6):599-613
The Kupferschiefer ore series, between the Lower Permian (Rotliegendes) terrestrial redbeds/volcanics and the Upper Permian (Zechstein) marine sequence, is developed as dark-grey organic matter-rich and metal sulphide-containing deposits (reduced zone) and as red-stained organic matter-depleted and iron oxide-bearing sediments (oxidized zone?=?Rote Fäule). The transition zone from oxidized to reduced rocks occurs both vertically and horizontally. This zone is characterized by sparsely disseminated remnant copper sulphides within hematite-bearing sediments, replacements of copper sulphides by iron oxides and covellite, and oxide pseudomorphs after framboidal pyrite. These textural features and copper sulphide replacements after pyrite in reduced sediments imply that the main oxide/sulphide mineralization postdated formation of an early-diagenetic pyrite. Hematite-dominated sediments locally contain enrichments of gold and PGE. The Kupferschiefer mineralization resulted from upward and laterally flowing fluids which oxidized originally pyritiferous organic matter-rich sediments to form hematitic Rote Fäule areas, and which emplaced base and noble metals into reduced sediments. It is argued that long-lived and large-scale lateral fluid flow caused the cross-cutting relationships, expansion of the hematitic alteration front, redistribution of noble metals at the outer parts of oxidized areas, and the location of copper orebodies directly above and around oxidized and gold-bearing areas. The Rote Fäule may be a guide to favourable areas for both the Cu-Ag and new Au-Pt-Pd Kupferschiefer-type deposits. 相似文献