Speleothems in gypsum caves and their paleoclimatological significance

This article highlights the relationship between speleothems growing inside gypsum caves and the particular climate that existed during their development. Speleothems in gypsum caves normally consist of calcium carbonate (calcite) or calcium sulphate (gypsum) and the abundance of such deposits greatly differs from zone to zone. Observations carried out over the last 20 years in gypsum caves subjected to very different climates (Italy, Spain, New Mexico, northern Russia, Cuba, Argentina) highlight wide variation in their cave deposits. In arid or semi-arid climates, the speleothems are mainly composed of gypsum, whilst in temperate, humid or tropical regions, carbonate formations are largely predominant. In polar zones no speleothems develop. These mineralogical details could be useful paleoclimatic indicators of climate change. The interpretation proposed is based on the fact that in gypsum karst the kind of speleothems deposited is determined by competition between the two principal mechanisms that cause precipitation of calcite and gypsum. These mechanisms are completely different: calcite speleothem evolution is mainly controlled by CO₂ diffusion, while gypsum deposits develop mostly due to evaporation. Therefore, the prevalence of one kind of speleothem over the other, and the relationship between the solution–precipitation processes of calcite and gypsum, may provide evidence of a specific paleoclimate. Additionally, other non-common deposits in gypsum caves like moonmilk, cave rafts and dolomite speleothems can be used as markers for the prevalence of long, dry periods in humid areas, seasonal changes in climate, or rainfall trends in some gypsum areas. Moreover, the dating of gypsum speleothems could contribute paleoclimatic data relating to dry periods when calcite speleothems are not deposited. In contrast, the dating of calcite speleothems in gypsum caves could identify former wet periods in arid zones.     

Pleistocene speleothems of Mallorca: implications for palaeoclimate and carbonate diagenesis in mixing zones

The Pleistocene speleothems of Sa Bassa Blanca cave, Mallorca, are excellent indicators of palaeoclimate variations, and are samples that allow evaluation of the products and processes of mixing‐zone diagenesis in an open‐water cave system. Integrated stratigraphic, petrographic and geochemical data from a horizontal core of speleothem identified two main origins for speleothem precipitates: meteoric‐marine mixing zone and meteoric‐vadose zone. Mixing‐zone precipitates formed at and just below the water–air interface of cave pools during interglacial times, when the cave was flooded as a result of highstand sea‐level. Mixing‐zone precipitates include bladed and dendritic high‐Mg calcite, microporous‐bladed calcite with variable Mg content, and acicular aragonite; their presence suggests that calcium‐carbonate cementation is significant in the studied mixing‐zone system. Fluid inclusion salinities, δ¹³C and δ¹⁸O compositions of the mixing‐zone precipitates suggest that mixing ratio was not the primary control on whether precipitation or dissolution occurred, rather, the proximity to the water table and degassing of CO₂ at the interface, were the major controls on precipitation. Thus, simple two‐end‐member mixing models may apply only in mixing zones well below the water table. Meteoric‐vadose speleothems include calcite and high‐Mg calcite with columnar and bladed morphologies. Vadose speleothems precipitated during glacial stages when sea level was lower than present. Progressive increase in δ¹³C and δ¹⁸O of the vadose speleothems resulted from cooling temperatures and more positive seawater δ¹⁸O associated with glacial buildup. Such covariation could be considered as a valid alternative to models predicting invariant δ¹⁸O and highly variable δ¹³C in meteoric calcite. Glacio‐eustatic oscillations of sea‐level are recorded as alternating vadose and mixing‐zone speleothems. Short‐term climatic variations are recorded as alternating aragonite and calcite speleothems precipitated in the mixing zone. Fluid‐inclusion and stable‐isotope data suggest that aragonite, as opposed to calcite, precipitated during times of reduced meteoric recharge.     

Speleothems from Mawsmai and Krem Phyllut caves,Meghalaya, India: some evidences on biogenic activities

The Mawsmai cave and Krem Phyllut caves, East Khasi hills, Meghalaya, India has so far not yet attracted the attention of geomicrobiologists. Observations and hypotheses on the possible influence of identified microorganisms for speleothem formations in Meghalaya are reported for the first time. XRD studies identified calcite in speleothems and gypsum in cave wall deposits as the dominant minerals. SEM-EDAX showed interesting microfabric features showing strong resemblance with fossilised bacteria, calcified filaments, needle calcite and numerous nano scale calcite crystals, highly weathered and disintegrated crystals of calcite, that point towards a significant microbial influence in its genesis. Thin section petrography showed laminated stromatolitic features. The microorganisms identified by conventional isolation and further evaluation of isolates by molecular techniques include Bacillus cereus, Bacillus mycoides, Bacillus licheniformis, Micrococcus luteus, and Actinomycetes. Microscopic observations also showed unidentifiable cocci and four unidentifiable strains of CaSO₄ (gypsum) precipitating bacteria. Experimental studies confirmed that these bacteria are able to precipitate calcium minerals (calcite, gypsum, minor amounts of dolomite) in the laboratory. These results allow us to postulate that species like these may contribute to active biogenic influence in the cave formations at Meghalaya.     

High‐resolution synchrotron X‐ray fluorescence investigation of calcite coralloid speleothems: Elemental incorporation and their potential as environmental archives

Synchrotron high‐resolution and micro‐X‐ray fluorescence elemental mapping of two coeval coralloid speleothems from Lamalunga Cave (Italy) are complemented with petrographic, morphological and microstratigraphic studies. The importance of these speleothems relies on their direct and indirect association with a complete Neanderthal skeleton (‘Altamura Man’) found inside the cave. The coralloids grew discontinuously between 64·6 ka and the Holocene and reveal exceptionally high concentrations of Mg, Sr and Si, particularly on convex surfaces, where evaporation is more intense. The incorporation of trace elements depends on several factors including location, shape and geometrical evolution during their growth, as well as climate and environmental parameters. This resulted in calcite precipitation with Sr compositions from 100 to 1200 ppm and an average concentration of 7000 ppm Mg. An unusually high Si content (up to 16%) is possibly derived from volcanic ash transported as particulate and in solution inside the cave. The most common fabrics observed consist of non‐fluorescent elongated columnar calcite forming clean isopachous bands and fluorescent fibre‐like crystals associated with laminated, lenticular bands high in Sr, Mg and Si. Variability in Sr, Mg and Si concentrations appears to induce fabric changes in the coralloids. Elongation and lattice distortion of the crystals was found to coincide with high Mg concentrations. The transition from compact elongated to open to fibre‐like, is here interpreted as due to high concentrations of Si and Sr, which are preferentially incorporated in the speleothem at crystal boundaries and intra‐laminae. It is here inferred that coralloid fabric changes and their elemental content potentially record local rainfall variations through time, with the clean compact calcite marking high infiltration and open fibre‐like and micrite fabrics recording dry periods.     

Monohydrocalcite,hydromagnesite, nesquehonite,dolomite, aragonite,and calcite in speleothems of the Fränkische Schweiz,Western Germany

The formation of calcite, aragonite, dolomite, hydromagnesite, and nesquehonite in speleothems of a small cave within dolostone may be compared with the formation of these carbonate minerals in much larger environments in which evaporation exceeds precipitation (salt lakes, tropical lagoons, sebkhas etc...). In all cases the formation and diagenetic alteration is mainly governed by the Mg/Ca-ratio of the solutions, from which precipitation (or transformation) takes place.The certain occurrence of monohydrocalcite in the speleothems and in technical incrustations lead to the conclusion, that this very rare mineral precipitates from solutions which are transported as aerosols.     

Cave air control on dripwater geochemistry, Obir Caves (Austria): Implications for speleothem deposition in dynamically ventilated caves

There are very few process studies that demonstrate the annual variation in cave environments depositing speleothems. Accordingly, we initiated a monitoring program at the Obir Caves, an Austrian dripstone cave system characterized by a seasonally changing air flow that results in a predictable pattern of high pCO₂ during summer and low pCO₂ in winter. Although similar seasonal changes in soil pCO₂ occur, they are not directly connected with the changes in the subsurface since the dripwaters are fed from a well-mixed source showing little seasonal variation. Cold season flushing by relatively CO₂-poor air enhances degassing of CO₂ in the cave and leads to a high degree of supersaturation of dripwater with regard to calcite. Forced calcite deposition during the cold season also gives rise to a pronounced pattern of synchronous seasonal variations in electrical conductivity, alkalinity, pH, Ca and δ¹³C_DIC which parallel variations recorded in δ¹³C_{cave air}. Chemical components unaffected by calcite precipitation (e.g., δD, δ¹⁸O, SiO₂, SO₄) lack a seasonal signal attesting to a long residence in the karst aquifer. Modeling shows that degassing of CO₂ from seepage waters results in kinetically-enhanced C isotopic fractionation, which contrasts with the equilibrium degassing shown from the Soreq cave in Israel. The Obir Caves may serve as a case example of a dripstone cave whose seepage waters (and speleothems) show intra-annual geochemical variability that is primarily due to chemical modification of the groundwater by a dynamic, bidirectional subsurface air circulation.     

Modeling speleothem δC variability in a central Sierra Nevada cave using C and Sr/Sr

Carbon isotopes in speleothems can vary in response to a number of complex processes active in cave systems that are both directly and indirectly related to climate. Progressing downward from the soil zone overlying the cave, these processes include soil respiration, fluid-rock interaction in the host limestone, degassing of CO₂ and precipitation of calcite upflow from the speleothem drip site, and calcite precipitation at the drip site. Here we develop a new approach to independently constrain the roles of water-rock interaction and soil processes in controlling stalagmite δ¹³C. This approach uses the dead carbon proportion (dcp) estimated from coupled ¹⁴C and ²³⁰Th/U measurements, in conjunction with Sr isotope analyses on stalagmite calcite from a central Sierra Nevada foothills cave in California, a region characterized by a highly seasonal Mediterranean-type climate, to determine the roles of water-rock interaction and soil processes in determining stalagmite δ¹³C. Increases in stalagmite dcp between 16.5 and 8.8 ka are coincident with decreased δ¹³C, indicating a varying yet substantial contribution from the soil organic matter (SOM) reservoir, likely due to significantly increased average age of SOM in the soil veneer above the cave during wet climatic intervals.We use geochemical and isotope mixing models to estimate the host-carbonate contribution throughout the δ¹³C time series and determine the degree of degassing and calcite precipitation that occurred prior to precipitation of stalagmite calcite. The degree of degassing and prior calcite precipitation we calculate varies systematically with other climate indicators, with less degassing and prior calcite precipitation occurring during wetter climatic intervals and more during drier intervals. Modeled δ¹³C values and degassing calculations suggest that some degree of prior calcite precipitation is necessary at all time intervals to explain measured stalagmite δ¹³C values, even during relatively wet intervals. These results illustrate the importance of constraining degassing and prior calcite precipitation in the interpretation of speleothem δ¹³C records, particularly those from caves that formed in seasonal semi-arid to arid environments.     

Speleothem preservation and diagenesis in South African hominin sites implications for paleoenvironments and geochronology

Plio‐Pleistocene speleothems from australopithecine‐bearing caves of South Africa have the potential to yield paleoenvironmental and geochronological information using isotope geochemistry. Prior to such studies it is important to assess the preservation of geochemical signals within the calcitic and aragonitic speleothems, given the tendency of aragonitic speleothems to recrystallize to calcite. This study documents the geochemical suitability of speleothems from the principal hominin‐bearing deposits of South Africa. We use petrography, together with stable isotope and trace element analysis, to identify the occurrence of primary aragonite, primary calcite, and secondary calcite. This study highlights the presence of diagenetic alteration at many of the sites, often observed as interbedded primary and secondary fabrics. Trace element and stable isotopic values distinguish primary calcite from secondary calcite and offer insights into geochemical aspects of the past cave environment. δ¹³C values of the primary and secondary calcites range from +6 to −9‰ and δ¹⁸O values range from −4 to −6‰. The data are thus typical of meteoric calcites with highly variable δ¹³C and relatively invariant δ¹⁸O. High carbon isotope values in these deposits are associated with the effects of recrystallization and rapid outgassing of CO₂ during precipitation. Mg/Ca and Sr/Ca ratios differ between primary and secondary calcite speleothems, aiding their identification. Carbon and oxygen isotope values in primary calcite reflect the proportion of C₃ and C₄ vegetation in the local environment and the oxygen isotope composition of rainfall. Primary calcite speleothems preserve the pristine geochemical signals vital for ongoing paleoenvironmental and geochronological research. © 2009 Wiley Periodicals, Inc.     

CO clumping in speleothems: Observations from natural caves and precipitation experiments

The oxygen isotope composition of speleothems is an important proxy of continental paleoenvironments, because of its sensitivity to variations in cave temperature and drip water δ¹⁸O. Interpreting speleothem δ¹⁸O records in terms of absolute paleotemperatures and δ¹⁸O values of paleo-precipitation requires quantitative separation of the effects of these two parameters, and correcting for possible kinetic isotope fractionation associated with precipitation of calcite out of thermodynamic equilibrium. Carbonate clumped-isotope thermometry, based on measurements of Δ₄₇ (a geochemical variable reflecting the statistical overabundance of ¹³C¹⁸O bonds in CO₂ evolved from phosphoric acid digestion of carbonate minerals), potentially provides a method for absolute speleothem paleotemperature reconstructions independent of drip water composition. Application of this new technique to karst records is currently limited by the scarcity of published clumped-isotope studies of modern speleothems. The only modern stalagmite reported so far in the literature yielded a lower Δ₄₇ value than expected for equilibrium precipitation, possibly due to kinetic isotope fractionation.Here we report Δ₄₇ values measured in natural speleothems from various cave settings, in carbonate produced by cave precipitation experiments, and in synthetic stalagmite analogs precipitated in controlled laboratory conditions designed to mimic natural cave processes. All samples yield lower Δ₄₇ and heavier δ¹⁸O values than predicted by experimental calibrations of thermodynamic equilibrium in inorganic calcite. The amplitudes of these isotopic disequilibria vary between samples, but there is clear correlation between the amount of Δ₄₇ disequilibrium and that of δ¹⁸O. Even pool carbonates believed to offer excellent conditions for equilibrium precipitation of calcite display out-of-equilibrium δ¹⁸O and Δ₄₇ values, probably inherited from prior degassing within the cave system.In addition to these modern observations, clumped-isotope analyses of a flowstone from Villars cave (France) offer evidence that the amount of disequilibrium affecting Δ₄₇ in a single speleothem can experience large variations at time scales of 10 kyr. Application of clumped-isotope thermometry to speleothem records calls for an improved physical understanding of DIC fractionation processes in karst waters, and for the resolution of important issues regarding equilibrium calibration of Δ₄₇ in inorganic carbonates.     

贵州凉风洞洞穴滴水水文水化学过程分析

通过对贵州荔波凉风洞5个滴水点进行为期1年的动态监测,表明除大气降雨携带的较少物质成份外,凉风洞滴水中的物质主要来源于土壤,同时,示踪结果显示出凉风洞滴水对大气降雨的响应较快,滴水的物质组成直接源自于洞穴环境。洞穴滴水的化学组成中元素含量的变化主要由水运移过程中水-土、水-岩作用导致的方解石溶解-沉淀过程所控制,稀释作用、水来源的差异或者活塞流产生了一定的效果,但其影响较弱,表明凉风洞滴水点的次生沉积物可能记录了环境变化信息。但水在洞穴顶板内运移过程中发生的水文地球化学过程(岩石的溶解、方解石沉淀作用过程)以及洞穴滴水响应大气降雨的时间尺度、水动力过程、水流形式等因素,影响到凉风洞洞穴次生沉积物过去环境记录指标。因此,岩溶次生沉积物过去环境变化指标的解译应该有洞穴滴水水动力地球化学过程的结果作为支撑。这些过程的清晰化可以更好地为研究洞穴环境次生沉积记录的高分辨率、短时间尺度的过去变化提供依据。     

Calcite from the Quaternary spring waters at Tylicz, Krynica, Polish Carpathians

At Tylicz, near Krynica Spa (Polish Carpathians), spelean deposits fill fissures and caverns in Eocene flysch rocks. They occur as: (1) clastic cave sediments transformed into hard crusts due to cementation by finely crystalline low-Mg calcite, (2) drusy calcite that covers crust surfaces and fills voids in the crust and (3) colloform calcite. Two varieties of drusy calcite are distinguished: acicular and columnar. The acicular calcite is built up of crystallites forming spherulitic fans or cones. In places it is syntaxially covered with colloform calcite. The drusy calcite is low-Mg ferroan calcite with non-ferroan subzones, whereas the colloform calcite is a low-Mg non-ferroan variety. The columnar calcite crystals form fan-like bundles. Cross-sections cut perpendicular to the c-axes of columnar crystals are equilateral triangular in shape, although some have slightly curved edges. The columnar crystals have steep rhombic terminations and most have curved triangular faces, i.e. gothic-arch calcite. Saddle crystals have also been observed. The columnar crystals are composed of radially orientated crystallites whose long dimension is parallel to the c-axis. The curved crystal faces of such polycrystals are interpreted as a result of differential growth rates of the crystallites. The spelean calcites precipitated from CO₂-saturated water. The high rate of CaCO₃ precipitation is thought to be responsible for the formation of radial structures. Finely crystalline calcite formed within pore spaces of clastic sediments close to the water-air interface, drusy calcite crystallized beneath the water-air interface, and colloform calcite precipitated from thin films of water.     

Origin and palaeoenvironmental significance of lamination in stalagmites from Katerloch Cave,Austria

The origin and environmental dependencies of lamination in stalagmites from Katerloch, common in speleothems from other cave sites, are examined in detail. Petrographic observations and chemical analyses (including isotopes) of stalagmites and modern calcite were combined with multi‐annual cave monitoring. All investigated stalagmites are composed of low‐Mg calcite and show white, porous laminae and typically thinner, translucent dense laminae. The binary lamination pattern results from changes in the calcite fabric: white, porous laminae are characterized by a high porosity and abundant fluid inclusions and also by enhanced vertical growth and thinning towards the flanks. Translucent, dense laminae exhibit a compact fabric and constant thickness of individual growth layers. U‐Th dating supports an annual origin of the lamination and the seasonally changing intensity of cave ventilation provides a robust explanation for the observed relationships between lamination, stable C isotopic compositions and trace elements (Mg, Sr and Ba). The seasonally variable air exchange, driven by temperature contrasts between the cave interior and outside atmosphere, modulates the rate and amount of CO₂ degassing from the drip water and affects the hydrochemistry and consequently the fabric of the precipitating calcite. Although cave air composition and drip rate are both major variables in controlling CO₂ degassing from the drip water, the seasonally changing ventilation in Katerloch exerts the primary control and the results suggest a secondary (amplifying/attenuating) influence of the drip rate. Drip rate, however, might be the controlling parameter for lamina development at cave sites experiencing only small seasonal cave air exchange. Importantly, the seasonally variable composition of drip water does not reflect the seasonal cycle of processes in the soil zone, but results from exchange with the cave atmosphere. The alternating porous and dense calcite fabric is the expression of a variable degree of lateral coalescence of smaller crystallites forming large columnar crystals. The white, porous laminae represent partial coalescence and form during the warm season: low calcite δ¹³C values are linked to low δ¹³C values of cave air and drip water during that time. This observation corresponds to times of reduced cave ventilation, high pCO₂ of cave air, low drip water pH, lower calcite supersaturation and typically high drip rates. In contrast, the translucent, dense laminae represent more or less complete lateral coalescence (inclusion‐free) during the cold season (high calcite, drip water and cave air δ¹³C values), i.e. times of enhanced cave ventilation, low cave air pCO₂, increased drip water pH, relatively high calcite supersaturation and typically low drip rates. In essence, the relative development of the two lamina types reflects changes in the seasonality of external air temperature and precipitation, with a strong control of the winter air temperature on the intensity of cave‐air exchange. Thick translucent, dense laminae are favoured by long, cold and wet winters and such conditions may be related closely to the North Atlantic Oscillation mode (weak westerlies) and enhanced Mediterranean cyclone activity during the cold season. Studies of speleothem lamination can thus help to better understand (and quantify) the role of seasonality changes, for example, during rapid climate events.     

Stable isotope studies of fluid inclusions in speleothems and their paleoclimatic significance

Fluid inclusions found trapped in speleothems (cave deposited travertine) are interpreted as samples of seepage water from which enclosing calcium carbonate was deposited. The inclusions are assumed to have preserved their D/H ratios since the time of deposition. Initial ¹⁸O/¹⁶O ratios can be inferred from δD because rain- and snow-derived seepage waters fall on the meteoric water line (δD = 8δ¹⁸O + 10). Estimates of temperature of deposition of the carbonate can be calculated from inclusion D/H ratios and δ¹⁸O of enclosing calcite in Pleistocene speleothems. For most speleothems investigated (0–200,000 yr old) δ¹⁸O of calcite appears to have decreased with increasing temperature of deposition indicating that the dominant cause of climate-dependent change in δ¹⁸O of calcite was the change in K_cw, the isotope fractionation equilibrium constant, with temperature; δ¹⁸O of meteoric precipitation generally increased with increasing temperature, but not sufficiently to compensate for the decrease in K_cw.     

Adsorbed silica in stalagmite carbonate and its relationship to past rainfall

Despite considerable work on other trace elements, the incorporation of dissolved silicon from cave waters into speleothems has not been previously investigated. In this study, the controls on dissolved Si in cave waters and on adsorbed Si in resulting speleothems are therefore investigated. Bedrock (dolomite), soil water, dripping water, and cave carbonates were retrieved from Heshang Cave situated in the central Yangtze valley of China and were subjected to analysis of dissolved Si content (plus accompanying Ca and Fe analyses). Soil waters have Si/Ca of 45.5 mmol/mol, compared to only 3.2 mmol/mol in the dolomite bedrock, demonstrating that >80% of the dissolved Si must come from dissolution of silicate minerals in the soil. Drip waters have a dissolved Si concentration of ≈4.2 μg/mL, similar to that in the overlying soil water. Actively growing cave carbonates have a Si/Ca of 0.075 mmol/mol suggesting a partition coefficient for incorporation of dissolved silicon of 0.0014, in good agreement with previous laboratory studies. Extrapolating the results of these laboratory studies to the cave environment suggests that changes in Si/Ca in cave carbonates are likely to be primarily controlled by changes in drip-water Si/Ca. The drip-water Si/Ca will, in turn, be controlled by the rate of wind-blown silicate supply; by soil weathering rates; by rainfall dilution; and by precipitation of calcite. The general expectation is that these effects combine to produce high Si/Ca in speleothems during times of low rainfall. A δ¹⁸O record from a Heshang Cave stalagmite which grew between 20 and 11 thousand years ago allows these controls to be tested. Correlation of high Si/Ca with high δ¹⁸O demonstrates that regional rainfall exerts significant (but not complete) control on speleothem Si/Ca. With further understanding, speleothem Si/Ca may provide a proxy for past rainfall to complement existing proxies such as δ¹⁸O and Mg/Ca.     

TEMPERATURE EFFECT ON PRECIPITATION OF CALCIUM CARBONATE FROM CALCIUM BICARBONATE SOLUTIONS AND ITS APPLICATION TO CAVERN ENVIRONMENTS

Solutions of calcium bicarbonate were allowed to lose carbon dioxide and evaporate to dryness under controlled temperature conditions. With filtered solutions prepared from spar calcite, precipitates were 100% calcite in the 2° to 100°C temperature range. When, in analogous experiments, coralline aragonite was the starting material, the precipitates were 100% calcite. Essentially the same was true when carbonate rocks from karst areas were used to prepare the experimental solutions. An artificially prepared mixture (maximum crystal size of about 7 u) of 70% aragonite and 30% calcite was also used in the study. The precipitates from this starting material were apparently affected by seed nuclei which passed through the filter. The stability of calcium carbonate seed nuclei appears to vary with temperature. Natural calcium bicarbonate solutions from caves yielded only calcite at 25°C. Calcite should be the dominant or only polymorph of CaCO₃ formed by the loss of carbon dioxide and evaporation of natural calcium bicarbonate solutions if temperature is the controlling factor. Since appreciable amounts of aragonite are found in many cave deposits, factors other than temperature must influence the polymorphs formed. POBEGUIN (1955) proposed that rapid evaporation and slow diffusion of solutions favor aragonite. If so, layers of aragonite and calcite in speleothems may reprsent alternate wet and dry paleoclimates. During these periods, rate of introduction of solution and rate of evaporation would change markedly.     

北京石花洞石笋微层层面有机物质的形成时间及机理初探

通过对北京石花洞滴水水溶性有机碳(DOC)近一个水文年的观测,发现不同点滴水DOC浓度均表现出明显的季节性变化,7月中旬均有一个大的主峰出现。初步说明中国北方石笋微层的层面物质沉积于7月雨季,主要来源于大的雨量对土壤中有机质的淋溶;洞穴顶板较薄的滴水点在5月和8月有明显的DOC次峰,可能与石笋亚年层形成有关。     

Meteoric phreatic speleothems and the development of cave stratigraphy: An example from Tounj Cave, Dinarides, Croatia

Speleothems occurring in some caves of the carbonate Dinarides line all channel surfaces, and have been deposited from meteoric waters under phreatic conditions. Such phreatic speleothemic deposition modifies common experience (l) that meteoric phreatic conditions cause dissolutional widening of cave voids, and (2) that speleothems imply vadose conditions. The phreatic speleothems described here postdate an early polygenetic evolution of the cave voids, and predate the last, vadose stage. They were likely produced during the late/postglacial warming period, when dissolved carbonate was amply supplied, and when there was much water available for saturation of underground voids. Phreatic speleothems may be used as a tool for time correlation of internal deposits, both within one cave and within a karst region. They indicate an important stage in the history of the ground-water regime of an area. In general, phreatic speleothems help in better understanding of the development of subterranean voids and related karst/palaeokarst.     

Cavity‐filling dolomite speleothems and submarine cements in the Ediacaran Dengying microbialites,South China: Responses to high‐frequency sea‐level fluctuations in an ‘aragonite–dolomite sea’

Speleothems, mostly composed of calcium carbonate, are widely present in modern karst‐originated caves, but have rarely been reported in palaeokarst systems. This study presents a novel type of dolomite speleothem and subsequent submarine dolomite cement, which are widely present in the upper Ediacaran Dengying Formation in the upper Yangtze area. These precipitated materials occur in the cavity system that cuts across several peritidal cycles. The interconnected cavity networks with irregular shapes, embayed walls, internal breccias on cavity floor and their preferential development in the shallower cycle tops (for example, tepee‐deformed beds) suggest that they were initially generated by subaerial dissolution. As the earliest infills, the hemispherical protrusions, icicle‐like pendants and ground‐up columns show similar morphological features and occurrence patterns to the cave popcorn, stalactites and stalagmites, respectively. Thus, these earliest infills are speleothems resulting from associated meteoric precipitation during subaerial exposure. The isopachous growth pattern of subsequent more extensive fibrous dolomite cements points to a submarine diagenetic environment in which they were precipitated. Microscopically, the micritic to micro‐crystalline dolomite, acicular dolomite in speleothems and the subsequent fibrous dolomite share similar crystal fabrics to metastable precursors (for example, Mg‐calcite). Meanwhile, the carbon‐oxygen isotope compositions of the speleothem and fibrous dolomite, although partly altered by burial diagenesis, share a large overlap with host rock and coeval marine carbonates all over the Yangtze Platform. For these reasons, these speleothems and fibrous cements are considered to have been initially precipitated as metastable carbonate precursors in meteoric and submarine environments, respectively, and stabilized during submarine mimetic dolomitization. The cyclic occurrence of cavity systems filled with speleothems and submarine cements reflects periodic subaerial exposure and marine flooding of broad tidal flat in the upper Yangtze area, driven by high‐frequency sea‐level fluctuations. Furthermore, the Neoproterozoic seawater chemistry that favoured early dolomitization of carbonate precursor mineralogies was an advantage for the preservation of fabrics from metastable precursor minerals.     

贵州七星洞系统中水文地球化学特征对滴水δ~(13)C_(DIC)的影响及其意义

2003年4月至2004年5月,笔者对贵州七星洞(QXD)进行了较为详细的监测,逐月采集了土壤水和洞穴滴水等样品,分别测定了样品的稳定碳同位素组成和水文地球化学参数。结果显示,9个滴水点同期的溶解无机碳同位素值(δ13CDIC)之间存在着大的差异,最大达6.9‰;δ13CDIC值偏重的Ⅰ组滴水,其Ca、Sr、HCO3、电导率(EC)和方解石饱和指数(SIC)等水文地球化学指标偏小,而Mg/Ca比值偏大,Ⅱ组则相反;不同滴水点的δ13CDIC值分别与相应滴水的Ca、Sr、HCO3、EC、Mg/Ca和SIC等水文地球化学指标之间存在较好的相关关系。进一步分析表明,与土壤水δ13CDIC平均值-9.9‰相比,Ⅰ组1#、2#、6#、7#和8#滴水点δ13CDIC值偏重4.5‰～5.7‰,主要是由大量的基岩溶解以及前期方解石沉积(prior calcite precipitation,PCP)共同作用的结果;Ⅱ组3#、4#、5#和9#滴水点δ13CDIC值偏重0.6‰～1.6‰,受基岩溶解和PCP过程影响较小,尤其是9#滴水点受影响最小。因此,若不考虑基岩溶解和PCP过程影响作用,将会极大地影响洞穴化学沉积物碳同位素记录的准确解释。     

漓江流域末次冰期以来气候环境变化研究进展

为更好地认识漓江流域过去气候环境变化,更好服务于漓江流域未来气候环境预测、生态环境建设及资源环境可持续发展,本文对漓江流域末次冰期以来的气候环境研究现状进行了总结和综述。总结了年代学、现代过程研究、古气候环境重建和古人类演化方面的进展及存在的问题,并对下一步的研究方向进行了分析和探讨。希望能促进华南地区过去气候环境变化研究,并对经济社会可持续发展提供借鉴和参考,助力桂林可持续发展创新示范区建设。