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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. ...

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That tinajita is (spanish.) see solution pan.?

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Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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Featured articles from other Geoscience Journals
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 trace-element (Keyword) returned 39 results for the whole karstbase:
Showing 1 to 15 of 39
Origin of the sedimentary deposits of the Naracoorte Caves, South Australia, , Forbes Ms, Bestland Ea,
The origin of the sediments located in the Naracoorte Caves (South Australia) was investigated via the analysis of strontium isotope ratios (87Sr/86Sr), elemental geochemistry, and mineralogy. Sedimentary deposits located in Robertson, Wet, Blanche and several other chambers in Victoria Cave are all variable mixes of fine sand and coarse silts, which display similar and consistent strontium isotope ratios (0.717-0.725). This suggests that over the 400[no-break space]ka time frame that these deposits span there has been minimal variation in the source of the clastic sediments. Increased strontium concentrations for these cave sediments correspond with increasing silt content, yet there is no correlation between 87Sr/86Sr ratios and silt content. This implies that the silt-sized component of the sediments is the main contributor of strontium to the cave sediments. Comparisons of 87Sr/86Sr with regional surficial deposits show a significant correlation between the cave sediments (avg: 0.7228; n = 27), the fine silt lunettes of the Bool Lagoon area (avg: 0.7224; n = 4), the sandy A horizons of the Coonawarra Red Brown Earths (RBEs; avg: 0.726; n = 5), and Holocene age podsolic sand deposits (0.723). These data suggest that there has been substantial flux from this group of deposits to the caves, as would be expected considering prevailing winds. This relationship is further supported by a strong correlation between many trace elements, including Ti, Zr, Ce, and Y; however, variations in clay mineralogy suggest that the fine silt-dominated lunettes and Padthaway RBEs were not significant contributors to the cave deposits. Hence, the detritus entering the caves was more than likely from areas proximal to the cave entrance and was dominated by medium grain-sized materials. Major regional deposits, including the coarser-grained, calcite-rich Bridgewater Formation sands, basalts from the lower SE, Padthaway Horst granites, Gambier limestone, and metamorphics from the Adelaide geosyncline show minimal correlation in 87Sr/86Sr ratios, elemental geochemistry, and mineralogy with the cave sediments, and are discounted as significant sources. In comparison, 87Sr/86Sr ratios for the Coorong silty sands (0.717-0.724), Lower Murray sands (0.727-0.730), and the medium size silt component of the Murray-Darling River system (0.71-0.72), compare favourably with the cave sediments. This relationship is further supported by similarities in elemental chemistry and mineralogy. Thus, much of the strontium-rich silt that is now located in the Naracoorte Cave sediments likely originated from the Murray-Darling basin. Over time, this material has been transported to the SE of South Australia, where it mixed with the medium sand component of the regressive dune ridge sequence, locally derived organic matter, limestone fragments, and fossil material to produce the unique deposits that we see evident in many of the chambers of the Naracoorte Cave system today

Trace-element partition coefficients in the calcite-water system and their paleoclimatic significance in cave studies, 1983, Gascoyne M,
Speleothems (stalactites, stalagmites) formed in limestone caves have been found to contain much information on the timing and intensity of past climates, from analysis of their U, Th, 13C and 18O contents. Because the incorporation of certain trace elements (e.g., Mg, Mn and Zn) in calcite is known to be temperature-dependent, it may be possible to use variations in trace-metal content of fossil speleothems as an alternative paleotem-perature indicator. Using specially developed ion-exchange sampling techniques, analysis of trace-metal content of seepage water and associated fresh calcite deposits in caves in Vancouver Island and Jamaica shows that Mg is distributed between phases in a consistent manner within the temperature regimes of the caves (7[deg] and 23[deg]C, respectively). Average values of the distribution coefficient for Mg are respectively 0.017 and 0.045 at these temperatures. These results indicate that the Mg content of calcite varies directly with temperature and in a sufficiently pronounced manner that a 1[deg]C rise in depositional temperature of a speleothem containing 500 ppm Mg, at ~10[deg]C, would be seen as an increase of ~35ppm Mg -- a readily determinable shift. Other factors affecting Mg content of a speleothem are considered

Petrography of the Lower Ordovician Ellenburger Group, both in deeply-buried subsurface cores and in outcrops which have never been deeply buried, documents five generations of dolomite, three generations of microquartz chert, and one generation of megaquartz. Regional periods of karstification serve to subdivide the dolomite into 'early-stage', which predates pre-Middle Ordovician karstification, and 'late-stage', which postdates pre-Middle Ordovician karstification and predates pre-Permian karstification. Approximately 10% of the dolomite in the Ellenburger Group is 'late-stage'. The earliest generation of late-stage dolomite, Dolomite-L1, is interpreted as a precursor to regional Dolomite-L2. L1 has been replaced by L2 and has similar trace element, O, C, and Sr isotopic signatures, and similar cathodoluminescence and backscattered electron images. It is possible to differentiate L1 from L2 only where cross-cutting relationships with chert are observed. Replacement Dolomite-L2 is associated with the grainstone, subarkose, and mixed carbonate-siliciclastic facies, and with karst breccias. The distribution of L2 is related to porosity and permeability which focused the flow of reactive fluids within the Ellenburger. Fluid inclusion data from megaquartz, interpreted to be cogenetic with Dolomite-L2, yield a mean temperature of homogenization of 85 6-degrees-C. On the basis of temperature/delta-O-18-water plots, temperatures of dolomitization ranged from approximately 60 to 110-degrees-C. Given estimates of maximum burial of the Ellenburger Group, these temperatures cannot be due to burial alone and are interpreted to be the result of migration of hot fluids into the area. A contour map of delta-O-18 from replacement Dolomite-L2 suggests a regional trend consistent with derivation of fluids from the Ouachita Orogenic Belt. The timing and direction of fluid migration associated with the Ouachita Orogeny are consistent with the timing and distribution of late-stage dolomite. Post-dating Dolomite-L2 are two generations of dolomite cement (C1 and C2) that are most abundant in karst breccias and are also associated with fractures, subarkoses and grainstones. Sr-87/Sr-86 data from L2, C1, and C2 suggest rock-buffering relative to Sr within Dolomite-L2 (and a retention of a Lower Ordovician seawater signature), while cements C1 and C2 became increasingly radiogenic. It is hypothesized that reactive fluids were Pennsylvanian pore fluids derived from basinal siliciclastics. The precipitating fluid evolved relative to Sr-87/Sr-86 from an initial Pennsylvanian seawater signature to radiogenic values; this evolution is due to increasing temperature and a concomitant evolution in pore-water geochemistry in the dominantly siliciclastic Pennsylvanian section. A possible source of Mg for late-stage dolomite is interpreted to be from the dissolution of early-stage dolomite by reactive basinal fluids

Carbonate chemistry of surface waters in a temperate karst region: the southern Yorkshire Dales, UK, 1992, Pentecost Allan,
A detailed study of surface water chemistry is described from an important limestone region in northern England. Major ions and pH were determined for 485 sites (springs, seeps, streams, rivers and lakes) during summertime. The saturation state of the waters with respect to calcite was determined as the calcite saturation ratio ([Omega]). An unexpectedly large number of samples were found to be supersaturated (65.5% of the 268 km of watercourses surveyed). As a consequence, several streams entering major cave systems were incapable of further limestone solution, at least during periods of low flow. Many waters were supersaturated from their source and some deposited travertine. A significant negative correlation was found between spring discharge and both ([Omega]) and pH. Supersaturation was caused primarily by atmospheric degassing, with some contribution from aquatic plant photosynthesis.The median total dissolved inorganic carbon and Ca concentrations were 2.49 and 1.35 millimoles 1-1 respectively. Calcium originated exclusively from limestone, and carbon dioxide mainly from the soil and dissolved limestone. South facing catchments provided springwaters with significantly higher levels of TDIC and Ca when compared with north facing catchments. The study suggests that acid rain made a measurable contribution to limestone dissolution.Carboniferous limestone denudation rates were estimated as 54 to 63 m3 km-2 a-1 (54 to 63 mm 1000 years-1). About 50% of the Mg came from limestone and the remainder, together with most K, Na, SO4 and Cl from precipitation.Concentrations of dissolved nutrients were low, medians for NO3, NH4, total PO4 and SiO3 were 24 [mu]mol, 1.4 [mu]mol, 0.64 [mu]mol and 15.5 [mu]mol 1-1 respectively. The concentration of a further 23 trace elements was determined

Palaeoclimate determination from cave calcite deposits, 1992, Gascoyne M,
Calcite deposits formed in limestone caves have been found to be an excellent repository of palaeoclimatic data for terrestrial environments. The very presence of a relict deposit indicates non-glacial conditions at the time of formation, and both 14C and uranium-series methods can be used to date the deposit and, hence, the age of these climatic conditions. Variations in 13C and 18O content of the calcite, in 2H and 18O content of fluid inclusions, in trace element concentrations and, more recently, in pollen assemblages trapped in the calcite, are all potentially available as synchronous palaeoclimatic indicators. Previous work has tended to concentrate mainly on abundance of deposits as a palaeoclimatic indicator for the last 300,000 years. This literature is briefly reviewed here, together with the theory and methods of analysis of the U-series and stable isotopic techniques. The combined use of U-series ages and 13C and 18O variations in cave calcites illustrates the potential for palaeoclimate determination. Previously unpublished results of stable isotopic variations in dated calcites from caves in northern England indicate the level of detail of stable isotopic variations and time resolution that can be obtained, and the complexity of interpretation that may arise. Tentative palaeoclimatic signals for the periods 90-125 ka and 170-300 ka are presented. More comprehensive studies are needed in future work, especially in view of the difficulty in obtaining suitable deposits and the ethics of cave deposits conservation

Geochemistry and water dynamics: Application to short time-scale flood phenomena in a small Mediterranean catchment .1. Alkalis, alkali-earths and Sr isotopes, 1997, Benothman D, Luck Jm, Tournoud Mg,
We report major, trace elements and Sr isotope data for water samples taken regularly during a four-day-long September flood of a Mediterranean river, the Vene (Herault, S. France). The objective is to combine all these data into a dynamic model that describes the origin(s) and movements of waters and their loads. This river drains the runoff from a small, mainly carbonate, partly karstified watershed with Miocene and Jurassic lithologies. The watershed is also impacted by both agricultural and urban activities. Both the dissolved and the particulate loads were analyzed. Concentrations of the dissolved components show major remobilization of almost all elements during the first few hours of the flood (water treatment plants and aerosol scavenging), followed by a sharp concentration decrease. Some major species return to their previous summer values (Ca, HCO3) while others reach low 'background' levels (Na, K, Cl, SO4). Some trace elements (Rb, Sr, Cs) show similar behaviour but (Ba) appears somewhat unaffected. Trace element concentrations and ratios define two main periods (three in the suspended particulate matter). Ratios do not allow distinguishing between the three main sources for the dissolved load in the first period (Miocene, Jurassic, water treatment plants), but clearly show the Jurassic karst influence later on. The Sr-87/Sr-86 Of the suspended particulate matter is more variable and more radiogenic than in the dissolved phase. Variations in concentration ratios and Sr isotope composition in particulates indicate the large and variable contribution of Miocene silicates with some carbonate. However, there is a need for another component with [Rb]/[Sr] higher than bedrocks, internal or external to the watershed, possibly due to differential erosion. Dissolved Ca and Mg fluxes during the flood were calculated at 0.26 ton and 0.029 ton/km(2), respectively. Even though the carbonate nature of the watershed restricts variability in Sr isotope composition in the dissolved load, we distinguish several endmembers: seawater(approximate to marine rain), Miocene marls, Jurassic limestones, water treatment plants (and possibly another attributable to fertilizers). Combined with major and trace element variational Sr isotope fluctuations indicate time-varying proportions of different water endmembers at the outflow and suggest a general dynamic model. Based on PCA (principal component analysis), a 3D representation allows to visualize the geochemical evolution of the Vene waters. In particular, Sr isotopes clearly indicate that the inflow of karstic waters during the flood was not continuous but occurred as a series of marked oscillations between flowing waters with chemical signature of Miocene lithologies and increasing flushes of deeper waters that interacted with Jurassic lithologies. (C) 1997 Elsevier Science B.V

Interactions between ground water and surface water in the Suwannee River Basin, Florida, 1997, Katz B. G. , Dehan R. S. , Hirten J. J. , Catches J. S. ,
Ground water and surface water constitute a single dynamic system in most parts of the Suwannee River basin due to the presence of karst features that facilitate the interaction between the surface and subsurface. Low radon-222 concentrations (below background levels) and enriched amounts of oxygen-18 and deuterium in ground water indicate mixing with surface water in parts of the basin. Comparison of surface water and regional ground water flow patterns indicate that boundaries for ground water basins typically do not coincide with surface water drainage subbasins. There are several areas in the basin where around water flow that originates outside of the Suwannee River basin crosses surface water basin boundaries during both low-flow and high-flow conditions. In a study area adjacent to the Suwannee River that consists predominantly of agricultural land use, 18 wells tapping the Upper Floridan aquifer and 7 springs were sampled three times during 1990 through 1994 for major dissolved inorganic constituents, trace elements, and nutrients. During a period of above normal rainfall that resulted in high river stage and high ground water levels in 1991, the combination of increased amounts of dissolved organic carbon and decreased levels of dissolved oxygen in ground water created conditions favorable for the natural reduction of nitrate by denitrification reactions in the aquifer. As a result, less nitrate was discharged by ground water to the Suwannee River

Petrography, strontium, barium and uranium concentrations, and strontium and uranium isotope ratios in speleothems as palaeoclimatic proxies: Soreq Cave, Israel, 1999, Ayalon A, Barmatthews M, Kaufman A,
The reconstruction of the palaeoclimate of the eastern Mediterranean region for the last 60 ka BP is based on the delta(18)O and delta(13)C variations of speleothems from Soreq Cave, Israel. Climatic conditions during most of the rime interval between 60 and 17 ka BP (the period equivalent to the last glacial) were relatively cold and dry, while they were warmer and wetter from 17 ka BP to the present. At similar to 17 ka BP, there was a major climatic change with a sharp increase in annual rainfall and temperature and a very wet period occurring between 8.5 and 7.0 ka BP. During the colder and drier period, large, detritus-free, preferentially oriented calcite crystals were deposited from slow-moving water. As a result of a sharp change in the hydrological regime at similar to 17 ka BP, fast-moving water started entrainment of the soil and carrying detrital material into the cave, and the calcite crystals deposited became small and anhedral. Coinciding with the petrographic and isotopic changes, a sharp drop occurred in the concentrations of strontium, barium and uranium, and in the ratios Sr-87/Sr-86 and (U-234/U-238)(0), which reached mini mum values during the wettest period. This drop reflects enhanced weathering of the soil dolomite host rock. During colder and drier periods, higher trace-element concentrations and higher isotopic ratios reflect an increase in the contribution of salts derived from exogenic sources (sea spray and aeolian dust), and a reduced contribution of weathering from the host dolomites

Speleothems and climate: a special issue of The Holocene, 1999, Lauritzen Stein Erik, Lundberg Joyce,
Speleothems (cave dripstones) are formed as a part of the meteoric water cycle and therefore vari ations in their growth rate and composition reflect environmental changes on the land surface above the cave. Since they are continental deposits, and possess a remarkably accurate dating potential, using TIMS U-series techniques, speleothems are important palaeoclimatic archives for the terrestrial environment, complementing the marine and ice-core records. The climatic proxies that can be deciphered from speleothems are growth rate, stable isotope composition (d18O, d13C), organic (humic) matter and trace element composition, as well as luminescent laminae, which may display annual rhythms. The nine papers in this special issue ofThe Holocene present the latest results in palaeoclimatic analysis from speleothems

Trace element variations in coeval Holocene speleothems from GB Cave, southwest England, 1999, Roberts Mark S. , Smart Peter L. , Hawkesworth Chris J. , Perkins William T. , Pearce Nicholas J. G. ,
We report trace element (Mg, Sr and Ba) records based on laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) from three coeval Holocene speleothems from Great Chamber in GB Cave, southwest England. The trace element records are placed on a common timescale on the basis of a suite of TIMS 230Th-234U ages. This permits assessment of the reproducibility of the trace element record in coeval speleothems. The trace element records are not coherent, raising dobuts over the reliability of individual trace element records as potential archives of palaeoenvironmental information. Mg/Sr in speleothem calcite has been proposed as a potential palaeothermometer as Mg partitioning into calcite from water is temperaturedependent, while Sr partitioning into calcite is temperature-independent. However, we present the results of calculations which demonstrate that the observed Mg/Sr values in the three stalagmites cannot have been produced by Holocene temperature changes alone and that other processes must play a dominant role. We present a model which suggests that the observed trace element variations in the three speleothems reflect hydrological mixing of waters in the epikarstic zone above the cave which have interacted with two geochemi cally distinct source rocks (calcite and dolomite)

Controls on trace element (Sr-Mg) compositions of carbonate cave waters: implications for speleothem climatic records, 2000, Fairchild Ij, Borsato A, Tooth Af, Frisia S, Hawkesworth Cj, Huang Ym, Mcdermott F, Spiro B,
At two caves (Clamouse, S France and Ernesto, NE Italy), cave drip and pool waters were collected and sampled at intervals over a 2-3 year period. Mg/Ca and Sr/Ca concentration ratios, corrected for marine aerosols, are compared with those of bedrocks and, in some cases, aqueous leachates of soils and weathered bedrocks. Cave waters do not lie along mixing lines between calcite and dolomite of bedrock carbonate, but typically show enhanced and covarying Mg/Ca and Sr/Ca. Four factors are considered as controlling processes. (1) The much faster dissolution rate of calcite than dolomite allows for the possibility of increase of Mg/Ca if water-rock contact times are increased during drier conditions. A theoretical model is shown to be comparable to experimental leachates. (2) Prior calcite precipitation along a flow path is a powerful mechanism for generating enhanced and covarying Mg/Ca and Sr/Ca ratios. This mechanism requires the solution to lose CO, into pores or caverns. (3) Incongruent dolomite dissolution has only limited potential and is best regarded as two separate processes of dolomite dissolution and calcite precipitation. (4) selective leaching of Mg and Sr with respect to Ca is shown to be important in leachates from Ernesto where it appears to be a phenomenon of calcite dissolution. In general selective leaching can occur whenever Ca is sequestered into precipitates due to freezing or drying of soils, or if there is derivation of excess Sr and Mg from non-carbonate species. The Ernesto cave has abundant water supply which in the main chamber is derived from a reservoir with year-round constant P-CO2 of around 10(-2.4) and no evidence of calcite precipitation in the karst above the cave. Two distinct, bur overlying trends of enhanced and covarying Mg/Ca and Sr/Ca away from the locus of bedrock compositions are due to calcite precipitation within the cave and, at a variable drip site, due to enhanced selective leaching at slow drip rates. Mg-enhancement in the first chamber is due to a more dolomitic bedrock and longer residence times. The Clamouse site has a less abundant water supply and presents geochemical evidence of prior calcite precipitation. both in the cave and in overlying porous dolomite/dedolomitized limestone bedrock. Initial P-CO2 values as high as 10(-1) are inferred. Experimental incubations of Clamouse soils which generated enhanced P-CO2 and precipitated CaCO3 had compositions similar to the karst waters. Calcite precipitation is inferred to he enhanced in drier conditions. Hydrological controls on cave water chemistry imply that the trace element chemistry of speleothems may be interpretable in palaeohydrological terms. Drier conditions tends to promote not only longer mean residence times (enhancing dolomite dissolution and hence Mg/Ca), but also enhances degassing and calcite precipitation leading to increased Mg/Ca and Sr/Ca. (C) 2000 Elsevier Science B.V. All rights reserved

Tertiary weathered sediments located immediately to the west of the harbor at Newhaven, Sussex, UK, were investigated by examination of major and trace elements by scanning electron microscope (SEM), microprobe, and inductively coupled plasma mass spectrometer (ICP-MS), and the mineralogy was studied by optical petrography, X-ray diffraction (XRD), transmission electron microscope (TEM), selective leaching, and thermodynamic modeling. Studied outcrops experienced acid leaching by sulfuric acid percolating downward through Tertiary sediments overlying Cretaceous chalk. The progressive neutralization of the percolating acid fluids resulted in 'sequentially' layered neoformation of minerals: jarosite, iron oxides, aluminous minerals (sulfates, oxyhydroxides), gypsum, and Fe-Mn oxides. Substantial agreement was found between field observations and mineral assemblages obtained by modeling with the program CHILLER. These results suggest that the initial assumptions on the weathering process and mechanisms are correct. The relevance and implications of this study in the modeling of future denudation and weathering processes of radioactive waste-disposal sites (both deeply buried sites for high-level waste and surface sites for low-level waste) are discussed. Neoformed phases, such as jarosite, aluminous minerals, and silico-aluminous gels may play a significant role in the efficient trapping of mobilized pollutant radionuclides

The role of evaporites in the genesis of base metal sulphide mineralisation in the Northern Platform of the Pan-African Damara Belt, Namibia: geochemical and fluid inclusion evidence from carbonate wa, 2000, Chetty D, Frimmel He,
The Otavi Mountain Land is a base metal sulphide ore province in northern Namibia where deposits are hosted by platform carbonates of the Otavi Group in a foreland fold-and-thrust belt on the northern edge of the Pan-African Damara Belt. Deposits have been classified as the Berg Aukas- or Tsumeb-types, based on differences in ore association? stratigraphic position and geochemistry of ores and gangue carbonates. Mineralisation at these deposits is accompanied by carbonate alteration in the form of dolomite and calcite veins, carbonate recrystallisation, calcitisation and carbonate silicification. Based on cathodoluminescence imaging, trace and rare earth element (REE), O and C isotope, and fluid inclusion data, a series of carbonate generations, constituting wall rock alteration around the Tsumeb and Kombat (Tsumeb-type) and Berg Aukas (Berg Aukas-type) deposits, was established. Similar data obtained on the recently discovered Khusib Springs deposit indicate a strong affinity to Tsumeb-type deposits. Tsumeb-type deposits are distinguished from Berg Aukas-type deposits by having trace element and REE concentrations that are significantly higher in the alteration products compared to the carbonate host rocks. Only around Tsumeb-type deposits a relative enrichment in light REE is noted for the hydrothermal carbonate generations that are cogenetic with the main stage of mineralisation. Microthermometric results from fluid inclusions in carbonate alteration phases and associated quartz indicate relatively high salinity (17-33 wt% NaCl equivalent) for the main mineralising and subsequent sulphide remobilisation stages at the deposits investigated. Estimated mineralisation temperatures are significantly higher for Tsumeb-type deposits (370-405 degrees C) with early sulphide remobilisation in Tsumeb at 275 degrees C, whereas they are lower at Berg Aukas (up to 255 degrees C). Fluid inclusion leachate analysis suggests that most of the observed salinity can be ascribed to dissolved, predominantly Ca- and Mg-carbonates and chlorides with subordinate NaCl. Na-Cl-Br leachate systematics indicate a derivation of the fluid salinity from the interaction with evaporitic rocks en route. Tsumeb-type mineralisation is interpreted to be derived from fluids expelled during Pan-African orogeny in the more intensely deformed internal zones of the Damara Belt further south. When the high salinity fluids reached the carbonate platform after having scavenged high concentrations of base metals, base metal sulphide precipitation occurred in zones of high porosity, provided by karst features in the carbonate sequence. Results obtained for the Berg Aukas-type deposits emphasise their derivation from basinal brines, similar to Mississippi Valley-type deposits, and confirm that mineralisation of the Berg Aukas- and Tsumeb-types are both spatially and temporally distinct

Seasonal variations in Sr, Mg and P in modern speleothems (Grotta di Ernesto, Italy), 2001, Huang Yiming, Fairchild Ian J. , Borsato Andrea, Frisia Silvia, Cassidy Nigel J. , Mcdermott Frank, Hawkesworth Chris J. ,
Sub-annual variations in trace element chemistry and luminescence have recently been demonstrated from speleothems and offer the potential of high-resolution palaeoclimatic proxies. However, no studies have yet examined microscopic trace element variations in relation to modern cave conditions. In this study, the spatial variations in trace element (Sr, Mg and P) concentrations in speleothems (a stalagmite and a soda straw stalactite) from the alpine Ernesto cave (temperature 6.60.1[deg]C) in a forested catchment in NE Italy have been studied using secondary ion mass spectrometry (SIMS) and compared with environmental parameters and waters in the modern cave. An annual lamination exists in the stalagmite and soda straw stalactite in the form of clear calcite with narrow visible layers, which are UV-fluorescent and interpreted to contain soil-derived humic/fulvic acids washed into the cave during autumn rains. Microanalyses were undertaken of seven annual laminae, probably deposited during the 1960s in the stalagmite, and seven laminae in the 1990s for the stalactite.The analysis results show that Sr consistently has a trough and P, a peak centred on the inclusion-rich layer. Mg shows mainly a negative covariation with Sr in laminae formed in the 1990s, but a positive covariation in the stalagmite formed in 1960s. The spatial scale of the main geochemical variations is the same as that of annual laminae of inclusion-poor and inclusion-rich couplets. Mass balance arguments are used to show that the P is inorganic in form and presumably occurs as individual phosphate ions within the calcite.Most drip waters show limited chemical variations, but a summer peak in trace elements in 1995 and a decrease in Mg/Ca in the following winter are notable. More pronounced covariations in Mg/Ca and Sr/Ca are shown by a site with highly variable drip rates where ratios increase at slow drip rates. The strongest seasonal variations are found in pool waters, where ratios increase reflecting significant Ca removal from the water into the calcite during the winter in response to seasonal PCO2 variations in cave air. Thus, the cave waters' compositions tend to reflect climate conditions, such that Mg/Ca and Sr/Ca are tentatively interpreted to be higher when climate conditions are dry.Combining results from the speleothems and cave water along with the behaviour of each trace species, Mg/Ca variations in the speleothems are considered to reflect their variation in the cave waters, whereas, Sr incorporation is also dependent on precipitation rate, in this case, mainly controlled by temporal variations in PCO2 in the cave (and conceivably, also by inhibitors such as phosphate). P adsorption (a fraction of which is subsequently incorporated within calcite) depends on aqueous phosphate concentration and water flux, both of which should increase during the autumn. Therefore, multiple trace element profiles in speleothems reflect multiple aspects of environment seasonality and conditions, and hence, a calibration against weather records is desirable to establish their palaeoclimatological meaning. The strong annual variation of trace elements, and particularly P, can provide chronological markers for high-resolution studies of other climate proxies, such as stable isotopes

Annual to sub-annual resolution of multiple trace-element trends in speleothems, 2001, Fairchild Ij, Baker Andy, Borsato Andr, Frisia Silv, Hinton Rw, Mcdermott Fran, Tooth Af,
This study aims to establish evidence for the widespread existence of preserved high-resolution trace element variations in speleothems that may have climatic significance. Ion microprobe analysis of speleothems reveals that annual to sub-annual variations in element chemistry exist at five, shallow western European cave sites (Crag Cave, County Kerry and Ballynamintra, County Waterford, Ireland; Uamh an Tartair, Sutherland, Scotland; Grotte Pere-Noel, Belgium; Grotta di Ernesto, NE Italy) with widely varying climatic, geomorphic and geological settings. The variations are not restricted to species (Mg, Sr and Ba) known to substitute directly for Ca in the calcite lattice, but include H, F, Na and P. Phosphorus (as phosphate) displays the greatest variability and may have the most significance as a proxy for the seasonal temperature cycle because of its role as a nutrient element. The technique allows estimation of growth rate of speleothems at any interval of interest, which is one of several possible uses in palaeoclimatology

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