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Speleology in Kazakhstan

Shakalov on 04 Jul, 2018
Hello everyone!   I pleased to invite you to the official site of Central Asian Karstic-Speleological commission ("Kaspeko")   There, we regularly publish reports about our expeditions, articles and reports on speleotopics, lecture course for instructors, photos etc. ...

New publications on hypogene speleogenesis

Klimchouk on 26 Mar, 2012
Dear Colleagues, This is to draw your attention to several recent publications added to KarstBase, relevant to hypogenic karst/speleogenesis: Corrosion of limestone tablets in sulfidic ground-water: measurements and speleogenetic implications Galdenzi,

The deepest terrestrial animal

Klimchouk on 23 Feb, 2012
A recent publication of Spanish researchers describes the biology of Krubera Cave, including the deepest terrestrial animal ever found: Jordana, Rafael; Baquero, Enrique; Reboleira, Sofía and Sendra, Alberto. ...

Caves - landscapes without light

akop on 05 Feb, 2012
Exhibition dedicated to caves is taking place in the Vienna Natural History Museum   The exhibition at the Natural History Museum presents the surprising variety of caves and cave formations such as stalactites and various crystals. ...

Did you know?

That blade is in a cave, a thin sharp projection jutting out from roof, wall, or floor, of which it is an integral part; generally the remains of a partition or bridge [10].?

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Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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Karst environment, Culver D.C.
Mushroom Speleothems: Stromatolites That Formed in the Absence of Phototrophs, Bontognali, Tomaso R.R.; D’Angeli Ilenia M.; Tisato, Nicola; Vasconcelos, Crisogono; Bernasconi, Stefano M.; Gonzales, Esteban R. G.; De Waele, Jo
Calculating flux to predict future cave radon concentrations, Rowberry, Matt; Marti, Xavi; Frontera, Carlos; Van De Wiel, Marco; Briestensky, Milos
Microbial mediation of complex subterranean mineral structures, Tirato, Nicola; Torriano, Stefano F.F;, Monteux, Sylvain; Sauro, Francesco; De Waele, Jo; Lavagna, Maria Luisa; D’Angeli, Ilenia Maria; Chailloux, Daniel; Renda, Michel; Eglinton, Timothy I.; Bontognali, Tomaso Renzo Rezio
Evidence of a plate-wide tectonic pressure pulse provided by extensometric monitoring in the Balkan Mountains (Bulgaria), Briestensky, Milos; Rowberry, Matt; Stemberk, Josef; Stefanov, Petar; Vozar, Jozef; Sebela, Stanka; Petro, Lubomir; Bella, Pavel; Gaal, Ludovit; Ormukov, Cholponbek;
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Your search for sulfides (Keyword) returned 31 results for the whole karstbase:
Showing 1 to 15 of 31
The role of hydrothermal karst processes in the emplacement of sulfide ores, 1982, Sassgustkiewicz Maria, D?u?y?ski Stanis?aw

Genesis of paleokarst and strata-bound zinc-lead sulfide deposits in a Proterozoic dolostone, northern Baffin Island, Canada, 1984, Olson R. A. ,
Society Cliffs Formation; episodes of karstification since its deposition. During the first karst episode an evaporite solution-collapse breccia formed ubiquitously on the western Borden Peninsula. During the second karst episode a holokarst developed and an integrated cave system was formed. The caves subsequently were filled with sulfides and carbonate minerals; several interesting sedimentary structures exist in the zinc-lead sulfide deposits. The ore fluid and contained metals are postulated to have been derived during a late-stage dewatering of the black shale that underlies the Society Cliffs Formation. Sulfide deposition may have been caused by chemical reduction of sulfate that existed in the ore fluid when the fluid entered hydrocarbon-filled caves. During the third and fourth episodes of karstification, only merokarst developed in the Society Cliffs Formation. Karst effects which formed during these episodes include oxidized sulfide deposits and surface solution corridors.--Modified journal abstract

The lead-zinc ore deposits of the Siding-Gudan mineral subdistrict Guangxi are part of the large Nanling district of South China, and hosted in Devonian carbonate rocks. The ore bodies occur significantly along main faults and fault zones, and concentrate up to 300 meters above the Cambrian/Devonian unconformity. Connected with hydrothermal karst, size and volume of the ore bodies increase in proximity to this unconformity. Moving from the unaffected host rocks to the center of the ore bodies, four zones can be discriminated by the mineral assemblage (pyrite, sphalerite, galena) as well as by the degree of ordering, Ca/Mg, and Fe/Mn ratios of different dolomites. Homogenization temperatures range from 80-100-degrees-C (Presqu'ile dolomite) to 230-260-degrees-C (massive sphalerite). The sulfides reveal delta-S-34 = -20 to parts per thousand, and fluid inclusions display a salinity of 5-12 wt % equivalent NaCl. The diagenetic and hydrothermal history is similar to that of classic Mississippi Valley Type (MVT) sulfide mineral deposits as, for example, Pine Point in Canada. Mineralization and remobilization of the sulfides took place during a wide time span from late Paleozoic through Mesozoic. Both processes are considered as an interaction of saline basinal brines ascended from the adjoining dewatering trough, and magmatic-hydrothermal fluids of several magmatic-tectonic events

Several kinds of base metal deposits occur in the lower Paleozoic of southwest Sardinia (Iglesiente-Sulcis mineral district). This paper deals with those deposits which are generally referred to as Permo-Triassic, because they accompany and postdate the Hercynian orogeny and are related to magmatic activity. A large number of previously published geochemical data, integrated with additional new data (Sr, Pb, O, C, and S isotopes), are reviewed and discussed in the frame of the late to post-Hercynian geologic evolution of southwest Sardinia. According to geological and mineralogical characteristics, three types of deposits can be distinguished: (1) skarn ores related to late Hercynian leucogranitic intrusions, (2) high-temperature veins, and (3) low-temperature veins and karst filling. Pervasive epigenetic dolomitization phenomena are geochemically related to the low-temperature deposits. Sr and Pb isotopes of the first and second types (0.7097-0.7140 Sr-87/Sr-86; 17.97-18.29 Pb-206/Pb-204; 38.11-38.45 Pb-208/Pb-204) are distinctly more radiogenic than those of the third type (0.7094-0.7115 Sr-87/Sr-86; 17.86-18.05 Pb-206/Pb-204; 37.95-38.19 Pb-208/Pb-204) which, in turn, are closer to Paleozoic ores and carbonates. Fluid inclusion data indicate that the fluids responsible for mineralization of the first and second types of deposits were hot and dilute (T(h)= 370-degrees-140-degrees-C; <5 wt % NaCl equiv). In contrast, relatively colder and very saline fluids (T(h)= 140-degrees-70-degrees-C; >20 wt % NaCl equiv) were responsible for the third type of mineralization, as well for epigenetic dolomitization of the Cambrian host rocks. O isotopes measured in minerals from the first two types (deltaO-18SMOW = 12.8-18.9 parts per thousand) are O-18 depleted with respect to the third type (deltaO-18SMOW = 15.9-22.1 parts per thousand). These data, coupled with fluid inclusion formation temperatures, indicate that the fluids responsible for the first two types of mineralization were O-18 enriched with respect to those of the third type and related hydrothermal phenomena. The deltaS-34CDT in sulfides of the first two types vary between 3.7 and 10.73 per mil, whereas the values of the third type range from 12.0 to 17.9 per mil. Late to post-Hercynian mineralization is thus explained as the result of three distinct, though partly superimposed, hydrothermal systems. System 1 developed closer to the late Hercynian leucogranitic intrusions and led to the formation of the first and subsequently the second type of mineralization. The relatively hot and diluted fluids had a heated meteoric, or even partly magmatic, origin. Metals were leached from an external, radiogenic source, represented either by Hercynian leucogranites or by Paleozoic metasediments. Sulfur had a partly magmatic signature. System 2 was characterized by very saline, colder fluids which promoted dolomitization, silicification, and vein and karst mineralization. These fluids share the typical characteristics of formation waters, even though their origins remain highly speculative. The hydrothermal system was mainly rock dominated, with only a minor participation of the external radiogenic source of metals. Sulfur was derived by recirculation of pre-Hercynian strata-bound ores. System 3 records the invasion of fresh and cold meteoric waters which precipitated only minor ore and calcite gangue. It may represent the further evolution of system 2, possibly spanning a time well after the Permo-Triassic. The timing of all these phenomena is still questionable, due to the poor geologic record of the Permo-Triassic in southwest Sardinia. Nevertheless, the hypothesized scenario bears many similarities with hydrothermal processes documented throughout the Hercynian in Europe and spanning the same time interval. A comparison with the latter mineralization and hydrothermal activities leads to the hypothesis that the first two types of mineralization are linked to late Hercynian magmatic activity, whereas the third type may be related to either strike-slip or tensional tectonics which, throughout Europe mark the transition from the Hercynian orogeny to the Alpine cycle

The Ozark region of the U.S. midcontinent is host to a number of Mississippi Valley-type districts, including the world-class Viburnum Trend, Old Lead Belt, and Tri-State districts and the smaller Southeast Missouri barite, Northern Arkansas, and Central Missouri districts. There is increasing evidence that the Ozark Mississippi Valley-type districts formed locally within a large, interconnected hydrothermal system that also produced broad fringing areas of trace mineralization, extensive subtle hydrothermal alteration, broad thermal anomalies, and regional deposition of hydrothermal dolomite cement. The fluid drive was provided by gravity flow accompanying uplift of foreland thrust belts during the Late Pennsylvanian to Early Permian Ouachita orogeny. In this study, we use chemical speciation and reaction path calculations, based on quantitative chemical analyses of fluid inclusions, to constrain likely hydrothermal brine compositions and to determine which precipitation mechanisms are consistent with the hydrothermal mineral assemblages observed regionally and locally within each Mississippi Valley-type district in the Ozark region. Deposition of the regional hydrothermal dolomite cement with trace sulfides likely occurred in response to near-isothermal effervescence of CO2 from basinal brines as they migrated to shallower crustal levels and lower confining pressures. In contrast, our calculations indicate that no one depositional process can reproduce the mineral assemblages and proportions of minerals observed in each Ozark ore district; rather, individual districts require specific depositional mechanisms that reflect the local host-rock composition, structural setting, and hydrology. Both the Northern Arkansas and Tri-State districts are localized by normal faults that likely allowed brines to rise from deeper Cambrian-Ordovician dolostone aquifers into shallower carbonate sequences dominated by limestones. In the Northern Arkansas district, jasperoid preferentially replaced limestones in the mixed dolostone-limestone sedimentary packages. Modeling results indicate that the ore and alteration assemblages in the Tri-State and Northern Arkansas districts resulted from the flow of initially dolomite-saturated brines into cooler limestones. Adjacent to fluid conduits where water/rock ratios were the highest, the limestone was replaced by dolomite. As the fluids moved outward into cooler limestone, jasperoid and sulfide replaced limestone. Isothermal boiling of the ore fluids may have produced open-space filling of hydrothermal dolomite with minor sulfides in breccia and fault zones. Local mixing of the regional brine with locally derived sulfur undoubtedly played a role in the development of sulfide-rich ore runs. Sulfide ores of the Central Missouri district are largely open-space filling of sphalerite plus minor galena in dolostone karst features localized along a broad anticline. Hydrothermal solution collapse during ore deposition was a minor process, indicating dolomite was slightly undersaturated during ore deposition. No silicification and only minor hydrothermal dolomite is present in the ore deposits. The reaction path that best explains the features of the Central Missouri sulfide deposits is the near-isothermal mixing of two dolomite-saturated fluids with different H2S and metal contents. Paleokarst features may have allowed the regional brine to rise stratigraphically and mix with locally derived, H2S-rich fluids

Evaporites, brines and base metals: What is an evaporite? Defining the rock matrix, 1996, Warren J. K. ,
This paper, the first of three reviews on the evaporite-base-metal association, defines the characteristic features of evaporites in surface and subsurface settings. An evaporite is a rock that was originally precipitated from a saturated surface or near-surface brine in hydrological systems driven by solar evaporation. Evaporite minerals, especially the sulfates such as anhydrite and gypsum, are commonly found near base-metal deposits. Primary evaporites are defined as those salts formed directly via solar evaporation of hypersaline waters at the earth's surface. They include beds of evaporitic carbonates (laminites, pisolites, tepees, stromatolites and other organic rich sediment), bottom nucleated salts (e.g. chevron halite and swallow-tail gypsum crusts), and mechanically reworked salts (such as rafts, cumulates, cross-bedded gypsarenites, turbidites, gypsolites and halolites). Secondary evaporites encompass the diagenetically altered evaporite salts, such as sabkha anhydrites, syndepositional halite and gypsum karst, anhydritic gypsum ghosts, and more enigmatic burial associations such as mosaic halite and limpid dolomite, and nodular anhydrite formed during deep burial. The latter group, the burial salts, were precipitated under the higher temperatures of burial and form subsurface cements and replacements often in a non-evaporite matrix. Typically they formed from subsurface brines derived by dissolution of an adjacent evaporitic bed. Because of their proximity to 'true' evaporite beds, most authors consider them a form of 'true' evaporite. Under the classification of this paper they are a burial form of secondary evaporites. Tertiary evaporites form in the subsurface from saturated brines created by partial bed dissolution during re-entry into the zone of active phreatic circulation. The process is often driven by basin uplift and erosion. They include fibrous halite and gypsum often in shale hosts, as well as alabastrine gypsum and porphyroblastic gypsum crystals in an anhydritic host. In addition to these 'true' evaporites, there is another group of salts composed of CaSO4 or halite. These are the hydrothermal salts. Hydrothermal salts, especially hydrothermal anhydrite, form by the subsurface cooling or mixing of CaSO4- saturated hydrothermal waters or by the ejection of hot hydrothermal water into a standing body of seawater or brine. Hydrothermal salts are poorly studied but often intimately intermixed with sulfides in areas of base-metal accumulations such as the Kuroko ores in Japan or the exhalative brine deeps in the Red Sea. In ancient sediments and metasediments, especially in hydrothermally influenced active rifts and compressional belts, the distinction of this group of salts from 'true' evaporites is difficult and at times impossible. After a discussion of hydrologies and 'the evaporite that was' in the second review, modes and associations of the hydrothermal salts will be discussed more fully in the third review

Vadose weathering of sulfides and limestone cave development-Evidence from eastern Australia., 1996, Osborne R. A. L.

Many significant limestone caves in eastern Australia (particularly New South Wales, Tasmania) are associated with sulfide deposits and other ore bodies. These deposits have a variety of origins (hydrothermal, paleokarst, volcaniclastic). The sulfides weather on exposure to oxygen - rich vadose seepage water, lowering the water pH and releasing sulfate and magnesium which can lead to the deposition of gypsum and aragonite speleothems. Removal of weathered ores and ore - bearing paleokarst sediments in the vadose zone is, in places, an important mechanism for the formation of large caverns.

Geology, geochemistry, and origin of the continental karst-hosted supergene manganese deposits in the western Rhodope massif, Macedonia, northern Greece, 1997, Nimfopoulos M. K. , Pattrick R. A. D. , Michailidis K. M. , Polya D. A. , Esson J. ,
Economic Mn-oxide ore deposits of commercial grade occur in the Rhodope massif near Kato Nevrokopi in the Drama region, Northern Greece. The Mn-oxide mineralization has developed by weathering of continental hypogene rhodochrosite-sulphide veins. The vein mineralization is confined by tectonic shear zones between marble and metapelites, extending laterally into the marble as tabular, pod or lenticular oreshoots (up to 50 m x 20 m x 5-10 m). Supergene oxidation of the hypogene mineralization led to the formation of in-situ residual Mn-oxide ore deposits, and secondary infills of Mn-oxide ore in embryonic and well developed karst cavities. Whole rock geochemical profiles across mineralized zones confirm the role of thrusts and faults as solution passageways and stress the importance of these structures in the development of hydrothermal and supergene mineralization at Kato Nevrokopi. Three zones an recognized in the insitu supergene veins: (A) a stable zone of oxidation, where immobile elements form (or substitute in) stable oxide mineral phases, and mobile elements are leached; (B) a transitional (active) zone in which element behavior is strongly influenced by seasonal fluctuations of the groundwater table and variations in pH-Eh conditions; and (C) a zone of permanent flooding, where variations in pH-Eh conditions are minimal. Zone (B) is considered as the source zone for the karst cavity mineralization. During weathering, meteoric waters, which were CO2-rich (P-CO2 similar to 10(-3.8) to 10(-1.4)) and oxygenated (fO(2) -10(-17) for malachite), percolated downward within the veins, causing breakdown and dissolution of sulfides and marble, and oxidation of rhodochrosite to Mn-oxides. Karat cavity formation was favored by the high permeability along thrust zones. Dissolved Mn2 was transported into karst cavities in reduced meteoric waters at the beginning of weathering (pH similar to 4-5), and as Mn(HCO3)(2) in slightly alkaline groundwaters during advanced weathering (pH similar to 6-8). Mn4? precipitation took place by fO(2) increase in ground waters, or pH increase by continuous hydrolysis and carbonate dissolution. In the well developed karst setting, some mobility of elements occurred during and after karst ore formation in the order Na>K>Mg>Sr>Mn>As>Zn>Ba>Al>Fe>Cu>Cd>Pb. (C) 1998 Canadian Institute of Mining, Metallurgy and Petrolem. Published by Elsevier Science Ltd. All rights reserved

The Vazante zinc mine, Minas Gerais, Brazil; constraints in willemitic mineralization and fluid evolution, 1999, Lena Virginia Soares Monteiro, Jorge Silva Bettencourt, Baruch Spiro, Rodnei Graca, And Tolentino Flavio De Oliveira
The Vazante Mine is located in the Vazante District, the largest zinc district in Brazil. The Vazante deposit consists dominantly of an unusual willemitic ore. Small sulfide bodies are tectonically imbricated with the willemitic ore, within the Vazante shear zone. Structural styles of deformation and petrographic and isotopic evidence indicate that willemitic mineralization and deformation occurred synchronously during the Neo-Proterozoic. Various generations of hydrothermal veins and hydraulic breccias may pre-date, accompany and overprint the mineralization. Ore-formation temperatures are deduced from stable isotope geothermometry and mineral chemistry of both sulfide bodies and willemitic ore. Temperatures during the main stage of mineralization range from 206 degrees C to 294 degrees C (willemitic ore) and 317 degrees C (sulfides), and reflect the prevailing metamorphic conditions within the shear zone. The fluid from which the gangue minerals of the sulfide bodies precipitated (at 250 degrees C) had an oxygen isotopic average value of delta 18 O = +19.4 per mil. This value appears to reflect the interaction of metamorphic fluid with the carbonate rocks of the Vazante formation. At 250 degrees C, the fluid in equilibrium with the vein mineral phases and willemitic ore assemblage exhibits a uniform oxygen isotopic composition, with an average value of delta 18 O = +11.5 per mil. The positive linear covariance of delta 18 O and delta 13 C ratios of the carbonates is most likely due to the mixing of metamorphic and meteoric fluids. The delta 34 S values of sulfides indicate a direct crustal origin for the sulfur. It is suggested that the sulfur is largely derived from pre-existing sulfide bodies and has been transported by metamorphic fluids. The willemitic ore may have originated from the precipitation of metal in sulfur-poor fluids under oxidized conditions, within the Vazante shear zone.

Vein and Karst Barite Deposits in the Western Jebilet of Morocco: Fluid Inclusion and Isotope (S, O, Sr) Evidence for Regional Fluid Mixing Related to Central Atlantic Rifting, 2000, Valenza Katia, Moritz Robert, Mouttaqi Abdellah, Fontignie Denis, Sharp Zachary,
Numerous vein and karst barite deposits are hosted by Hercynian basement and Triassic rocks of the western Jebilet in Morocco. Sulfur, oxygen, and strontium isotope analyses of barite, combined with fluid inclusion microthermometry on barite, quartz, and calcite were used to reveal the nature and source of the ore-forming fluids and constrain the age of mineralization. The{delta} 34S values of barite between 8.9 and 14.7 per mil are intermediate between the sulfur isotope signatures of Triassic evaporites and Triassic-Jurassic seawater and lighter [IMG]f1.gif' BORDER='0'>, probably derived from the oxidation of dissolved H2S and leaching of sulfides in the Hercynian basement. The 87Sr/86Sr ratios of barite between 0.7093 and 0.7130 range between the radiogenic strontium isotope compositions of micaceous shale and sandstone and the nonradiogenic isotopic signature of Triassic to Jurassic seawater and Cambrian limestone. The{delta} 18O values of barite between 11 and 15 per mil (SMOW) support mixing between two or more fluids, including Late Triassic to Jurassic seawater or a water dissolving Triassic evaporites along its flow path, hot basinal, or metamorphic fluids with{delta} 18O values higher than 0 per mil and/or meteoric fluids with{delta} 18O values lower than 0 per mil. The general trend of decreasing homogenization temperatures and initial ice melting temperatures with increasing salinities of H2O-NaCl {} CaCl2 fluid inclusions trapped in barite, quartz, and calcite indicates that a deep and hot basinal fluid with salinities lower than 6 wt percent NaCl equiv might have mixed with a cooler surficial solution with a mean salinity of 20 wt percent NaCl equiv. Calcium was leached from the Cambrian limestone and the clastic and mafic volcanic rocks of the Hercynian basement. Alkali feldspars and micas contained in the Cambrain sandstones provided most of the Ba to the hydrothermal system. Vein and karst deposits are modeled as a two-component mixing process in which the temperature and the S and Sr isotope composition of the end members changed during the 220 to 155 Ma interval. The hot basinal fluid remained volumetrically dominant during the entire mineralization process. Differences in mean S, O, and Sr isotope compositions among the barite families are interpreted as reflecting differences in mineralization age. Most barite deposits formed before the Kimmeridgian, except for north-south-oriented vein barite, karst barite, and barite cement in the conglomeratic Upper Jurassic, which were deposited later, possibly around 155 Ma. Similar genetic processes have been described for late Paleozoic to Mesozoic F-Ba vein deposits in western Europe. The vein and karst barite in the western Jebilet of Morocco reveals a wide-scale regional mineralization event related to Central Atlantic rifting

Speleogenesis in the Picos de Europa massif, Northern Spain, 2000, Fernandezgibert E. , Calaforra J. M. , Rossi C.
The Picos de Europa mountain range in Northern Spain represents one of the most important alpine karsts in the world, containing a great concentration of deep limestone caves. It comprises Carboniferous limestones with thicknesses up to 2000 m and severely deformed by tectonic action. The structure and geological evolution, fracturing and Quaternary glaciation are among the main factors influenced the development of the caves. This paper proposes a speleogenetic model of the evolution, with an initial stage during which a Permo-Triassic cover provided semiconfinement for the entire carbonate series. Under these circumstances, the earliest known phreatic conduits were formed. Occasional relict sediments in them are related to the erosion of the cover. During the second stage, with the uplift of the massif, the cover was eroded and vadose conditions established; they were linked to glacial processes that intensified karstification, creating an unsaturated zone almost 2000 m thick. The karstification and vadose entrenchment in this zone are especially marked along preferential flow paths coinciding with pre-existing dolomitized and sulfide-mineralized fractures in the massif. These fractures may also have played a precursor role in the karstic evolution of the massif, as the source for more aggressive waters with a higher content of weak acids due to the oxidation of sulfides.

Sulfide-bearing palaeokarst deposits at Lune River Quarry, Ida Bay, Tasmania, 2001, Osborne R. A. L. , Cooper I. B. ,
The Lune River Quarry at ida Bay. Tasmania exposes numerous palaeokarst features developed in the Ordovician Gordon Limestone. These palaeokarst features contain carbonate and siliciclastic deposits probably representing Late Devonian to early Late Carboniferous and Late Carboniferous karstification and sedimentation. Five facies of palaeokarst deposits are recognised, namely megabreccia, graded-bedded carbonate, laminated sandstone/siltstone, diamictite/quartz-lithic sandstone and coarse crystalline calcite. Pyrite, dolomite and sphalerite were emplaced in the palaeokarst deposits after the Carboniferous. These deposits are probably associated with a phase of hydrothermal cave development in Exit Cave, which adjoins the quarry. Pyrite weathering accounts for the abundance of gypsum speleothems and cave breakdown in Exit Cave

Genesis of the Dogankuzu and Mortas Bauxite Deposits, Taurides, Turkey: Separation of Al, Fe, and Mn and Implications for Passive Margin Metallogeny, 2002, Ozturk Huseyin, Hein James R. , Hanilci Nurullah,
The Taurides region of Turkey is host to a number of important bauxite, Al-rich laterite, and Mn deposits. The most important bauxite deposits, Do[g]ankuzu and Morta[s], are karst-related, unconformity-type deposits in Upper Cretaceous limestone. The bottom contact of the bauxite ore is undulatory, and bauxite fills depressions and sinkholes in the footwall limestone, whereas its top surface is concordant with the hanging-wall limestone. The thickness of the bauxite varies from 1 to 40 m and consists of bohmite, hematite, pyrite, marcasite, anatase, diaspore, gypsum, kaolinite, and smectite. The strata-bound, sulfide- and sulfate-bearing, low-grade lower part of the bauxite ore bed contains pyrite pseudomorphs after hematite and is deep red in outcrop owing to supergene oxidation. The lower part of the bauxite body contains local intercalations of calcareous conglomerate that formed in fault-controlled depressions and sinkholes. Bauxite ore is overlain by fine-grained Fe sulfide-bearing and calcareous claystone and argillaceous limestone, which are in turn overlain by massive, compact limestone of Santonian age. That 50-m-thick limestone is in turn overlain by well-bedded bioclastic limestone of Campanian or Maastrichtian age, rich with rudist fossils. Fracture fillings in the bauxite orebody are up to 1 m thick and consist of bluish-gray-green pyrite and marcasite (20%) with bohmite, diaspore, and anatase. These sulfide veins crosscut and offset the strata-bound sulfide zones. Sulfur for the sulfides was derived from the bacterial reduction of seawater sulfate, and Fe was derived from alteration of oxides in the bauxite. Iron sulfides do not occur within either the immediately underlying or overlying limestone. The platform limestone and shale that host the bauxite deposits formed at a passive margin of the Tethys Ocean. Extensive vegetation developed on land as the result of a humid climate, thereby creating thick and acidic soils and enhancing the transport of large amounts of organic matter to the ocean. Alteration of the organic matter provided CO2 that contributed to formation of a relatively 12C-rich marine footwall limestone. Relative sea-level fall resulted from strike-slip faulting associated with closure of the ocean and local uplift of the passive margin. That uplift resulted in karstification and bauxite formation in topographic lows, as represented by the Do[g]ankuzu and Morta[s] deposits. During stage 1 of bauxite formation, Al, Fe, Mn, and Ti were mobilized from deeply weathered aluminosilicate parent rock under acidic conditions and accumulated as hydroxides at the limestone surface owing to an increase in pH. During stage 2, Al, Fe, and Ti oxides and clays from the incipient bauxite (bauxitic soil) were transported as detrital phases and accumulated in the fault-controlled depressions and sinkholes. During stage 3, the bauxitic material was concentrated by repeated desilicification, which resulted in the transport of Si and Mn to the ocean through a well-developed karst drainage system. The transported Mn was deposited in offshore muds as Mn carbonates. The sulfides also formed in stage 3 during early diagenesis. Transgression into the foreland basin resulted from shortening of the ocean basin and nappe emplacement during the latest Cretaceous. During that time bioclastic limestone was deposited on the nappe ramp, which overlapped bauxite accumulation

Patterns of dissolutional porosity in carbonate rocks, 2003, Palmer, A. N.

This paper reviews the hydrochemical processes that determine the patterns of caves and other solutional features within carbonate rocks. The model presented relies on the functional relationships expressed by chemical mass balances, flow equations, and kinetic expressions for dissolution rate. Although it shares many aspects of purely conceptual models and is backed by field evidence, its quantitative basis places it into the realm of analytical models.
The conclusions merely summarize earlier work (mainly Palmer, 1981, 1991). Solutional enlargement of caves and other karst features is highly selective in water that is close to equilibrium with dissolved carbonate minerals, enlarging only the most favorable openings – i.e. those that transmit the greatest discharge. This is characteristic of long flow paths within a typical karst aquifer. In contrast, solutional enlargement will be rather uniform along many competing flow paths where there is (1) high discharge, (2) sustained steep hydraulic gradients, (3) short flow paths, or (4) local renewal of aggressiveness by mixing, oxidation of sulfides, etc. These conditions produce maze caves and epikarstic networks. In general, this condition prevails if Q/rL > 0.001 cm/sec (tubes), or /bL > 0.001 cm/sec (fissures), where Q = discharge, r = tube radius, b = long dimension of fissure cross section, and L = distance of flow from where the initial aggressive solution comes in contact with the carbonate rock.

The Shaimerden Supergene Zinc Deposit, Kazakhstan: A Preliminary Examination, 2003, Boland Mb, Kelly Jg, Schaffalitzky C,
The Shaimerden supergene zinc deposit in the southern Urals Mountains is located in the province of Kostanai in northwest Kazakhstan. It lies at the southern end of the Kostanai megasyncline, a north-northeast-trending, structurally controlled area of lower Paleozoic clastic and carbonate sedimentary rocks and volcanic rocks. A zinc-lead resource estimated at 4,645,100 tonnes at 21.06 percent Zn has been defined. The deposit is hosted within a sequence of intertidal to open-marine carbonates and evaporites of Visean (Early Carboniferous) age. Although drilling to date has not intersected a fault, significant faulting in the area is suggested by the presence of polymict debris flows comprising a wide range of carbonate facies and by large variations in micropaleontologic dates. Sulfide deposits replaced hydrothermally dolomitized carbonates and were subsequently reworked into polymict conglomerates of probable Carboniferous age that were deposited in a marine environment. Weathering of the sulfide mineral deposits took place during the Triassic Period, following uplift during the late Paleozoic. The weathering occurred in situ, and small intervals of relict sulfides were preserved in the center of the deposit. The degree of weathering increases outward from the center of the deposit, which passes from massive sulfide to massive hemimorphite-smithsonite to weathered clays with hemimorphite-smithsonite fragments. The supergene minerals are overlain by bauxitic clays of Cretaceous age and Quaternary silty soils and sands

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