Gypsum facies transitions in basin-marginal evaporites: middle Miocene (Badenian) of west Ukraine

In the middle Miocene Badenian gypsum basin of the Carpathian Foredeep, west Ukraine, three main zones of gypsum development occur in the peripheral parts of the basin. Zone I consists entirely of stromatolitic gypsum formed in a nearshore zone. Zone II is located more basinward and is characterized by stromatolitic gypsum in the lower part of the section, overlain by a sabre gypsum unit. Zone III occurs in still more basinward areas and is characterized by giant gypsum intergrowths (or secondary nodular gypsum pseudomorphs of these) in the lowermost part, overlain by stromatolitic gypsum, sabre gypsum and then by clastic gypsum units. Correlation between these facies and zones has been achieved using lithological marker beds and surfaces. Of particular importance for correlation is a characteristic marker bed (usually 20–40 cm thick) of cryptocrystalline massive gypsum occurring in zones II and III. The marker was not distinguished in zone I, possibly because this bed is older than the entire gypsum section of that zone. These new results strongly suggest that the deposition of giant gypsum intergrowth facies and stromatolitic gypsum facies was coeval. In some sections of zones I and II, limestone intercalations have been recorded within the upper part of the gypsum sections. Considerable scatter of the δ¹⁸O and δ¹³C values of these limestones indicates variable diagenetic overprints of marine carbonates, but a marine provenance of the limestones is confirmed by microfacies analysis. Some of the limestones are coeval with an intercalation of gypsarenitic, mostly laminated gypsum occurring in the sabre gypsum unit of zones II and III. Badenian gypsum formed in extremely shallow‐water to subaerial environments on broad, very low relief areas of negligible brine depth, which could be affected by rapid transgressions. Stable isotope (δ³⁴S, δ¹⁸O) studies of the gypsum demonstrate that the sulphate was of sea‐water origin or was derived from dissolution of Miocene marine evaporites. Investigations of individual inclusions in the gypsum indicate decreased water salinity when compared with modern marine‐derived, calcium sulphate‐saturated water. Groundwater influences are indicated by high calcium sulphate contents of the brines in the evaporite basin. The chemical composition of Badenian waters was thus a mixture of relic sea water (depleted in NaCl), groundwater (enriched in calcium sulphate) and surface run‐off.     

Origin and evolution of major salts in the Darling pans,Western Cape,South Africa

Sediment and water samples from 12 saline pans on the semi-arid west coast of South Africa were analysed to determine the origin of salts and geochemical evolution of water in the pans. Pans in the area can be subdivided into large, gypsiferous coastal pans with 79–150 g/kg total dissolved salt (TDS), small inland brackish to saline (2–64 g/kg TDS) pans and small inland brine (168-531 g/kg TDS) pans that have a layer of black sulphidic mud below a halite crust. The salinity of coastal pan waters varies with the seasonal influx of dilute runoff and dissolution of relict Pleistocene marine evaporite deposits. In contrast, inland pans are local topographic depressions, bordered on the north by downslope lunette dunes, where solutes are concentrated by evaporation of runoff, throughflow and groundwater seepage. The composition of runoff and seepage inflow waters is determined by modification of coastal rainfall by weathering, calcite precipitation and ion exchange reactions in the predominantly granitic catchment soils. Evaporation of pan waters leads to precipitation of calcite, Mg–calcite, dolomite, gypsum and halite in a distinct stratigraphic succession in pan sediments. Bicarbonate limits carbonate precipitation, Ca limits gypsum precipitation and Na limits halite precipitation. Dolomitisation of calcite is enhanced by the high Mg/Ca ratio of brine pan waters. Brine pan waters evolve seasonally from Na–Cl dominated brines in the wet winter months to Mg–Cl dominated brines in the dry summer months, when 5–20 cm thick halite crusts cover pan surfaces. Pan formation was probably initiated during a drier climate period in the early Holocene. More recent replacement of natural vegetation by cultivated land may have accelerated salt accumulation in the pans.     

Foraminiferal record of marine transgression during deposition of the Middle Miocene Badenian evaporites in Central Paratethys (Borków section,Polish Carpathian Foredeep)

Benthic and planktonic foraminifera from a marly clay intercalation sandwiched between mid‐Badenian (Middle Miocene) gypsum deposited in an environment of an evaporitic shoal (<1 m deep) at Borków (southern Poland) indicate a major marine flooding event in the previously isolated Carpathian Foredeep Basin (Central Paratethys). After this very short‐term environmental change, benthic foraminifers started to colonize a new niche which was previously defaunated, and the pattern of benthic foraminiferal colonization is similar to that related to the reflooding which terminated the Badenian evaporite deposition. The benthic foraminifer assemblages are composed of pioneer, opportunistic, r‐selected species dominated by elphidiids. The connection of the Carpathian Foredeep Basin with the marine reservoir was short‐lived. The marly clay intercalations in evaporite sequences originating in bared basins can thus register major environmental changes.     

Palaeogeographic and burial controls on anhydrite genesis: the Badenian basin in the Carpathian Foredeep (southern Poland, western Ukraine)

The Badenian (Middle Miocene) Ca-sulphate deposits of the fore-Carpathian basin – including the shelf and adjacent salt depocentre – have undergone varying degrees of diagenetic change: they are preserved mainly as primary gypsum in the peripheral part of the platform, whereas toward the centre of the basin, where great subsidence occurred during the Miocene, they have been totally transformed into anhydrite. The facies variation and sequence of Badenian anhydrites reflect different genetic patterns of two members of the Ca-sulphate formation. In the lower member (restricted to the platform), anhydrite formed mainly by synsedimentary anhydritization (via nodule formation), whereas in the upper member (distributed throughout the platform and depocentre) the various gypsum/anhydrite lithofacies display a continuum of distinctive anhydrite type-fabrics. These fabrics are based on petrographic features and show from the centre to the margin: (1) syndepositional, interstitial growth of displacive anhydrite; (2) early diagenetic, displacive to replacive (by replacement of former gypsum) anhydrite formation near the depositional surface; (3) early diagenetic, displacive to replacive anhydrite formation during shallow burial; and (4) late-diagenetic (and only partial) replacement of gypsum at deeper burial. The cross-shelf lateral relations of anhydrite lithofacies and fabrics suggest that the diagenesis developed as a diachronous process. These fabrics of the upper member reflect both palaeogeographic (linked to different parts of the basin) and burial controls. Anhydrite growth started very early in the basin centre, presumably related to high-salinity pore fluids; anhydritization prograded updip toward the shelf (landward in a generalized cross-section through the basin). The intensity of gypsum replacement by anhydrite was progressively attenuated landward by a decrease in the salinity of the pore fluids. In each part of the basin, the anhydrite fabric was also controlled by the texture and degree of lithification of the fine-grained primary gypsum lithofacies. Recrystallization of these anhydrite fabrics during late diagenesis, linked to deeper burial conditions, is insignificant, allowing reconstruction of the original anhydritization pattern.     

Origin of polyhalite deposits in the Zechstein (Upper Permian) Zdrada platform (northern Poland)

Polyhalite deposits in the Zechstein (Upper Permian) of northern Poland occur in the Lower Werra Anhydrite. In the Zdrada Sulphate Platform, the polyhalite appears to be a very early replacement of anhydrite. The replacement was caused by the halite-precipitating brines which contained potassium and magnesium ions. The formation of polyhalite was preceded by the syndepositional anhydritization of the original gypsum deposit which has often preserved its primary textures. This anhydritization on the platform and its slopes was a reaction of the precipitated gypsum in a hydrologically open evaporite basin, with brines of salt basins adjacent to the sulphate platform. These brines, when nearly saturated with respect to halite, and potassium and magnesium rich, reacted with anhydrite to precipitate polyhalite along the slopes of the Zdrada Platform. The oxygen and sulphur isotopic compositions of sulphate evaporites indicate that marine solutions were the only source of sulphate ions supplied to the Zechstein basin, and that anhydrite was transformed to polyhalite by reaction with marine brines more concentrated than those that precipitated precursor calcium sulphate minerals.     

Evaporative systems and diagenetic patterns in the Calatayud Basin (Miocene,central Spain)

This paper concerns the evaporite units, depositional systems, cyclicity, diagenetic products and anhydritization patterns of the Calatayud Basin (nonmarine, Miocene, central Spain). In outcrop, the sulphate minerals of these shallow lacustrine evaporites consist of primary and secondary gypsum, the latter originating from the replacement of anhydrite and glauberite. In the evaporative systems of this basin, gypsiferous marshes of low salinity can be distinguished from central, saline lakes of higher salinity. In the gypsiferous marsh facies, the dominant, massive, bioturbated gypsum was partly replaced by synsedimentary chert nodules and siliceous crusts. In the saline lake facies, either cycles of gypsiferous lutite‐laminated gypsarenite or irregular alternations of laminated gypsum, nodular and banded glauberite, thenardite and nodular anhydrite precipitated. Early replacement of part of the glauberite by anhydrite also occurred. Episodes of subaerial exposure are represented by: (1) pedogenic carbonates (with nodular magnesite) and gypsiferous crusts composed of poikilitic crystals; and (2) nodular anhydrite, which formed in a sabkha. Additionally, meganodular anhydrite occurs, which presumably precipitated from ascending, highly saline solutions. The timing of anhydritization was mainly controlled by the salinity of the pore solutions, and occurred from the onset of deposition to moderate burial. Locally, a thick (>200 m) sequence of gypsum cycles developed, which was probably controlled by climatic variation. A trend of upward‐decreasing salinity is deduced from the base to the top of the evaporite succession.     

Depositional environments of marine-dominated bedded halite, Permian San Andres Formation, Texas

The interpretation of the depositional environments in which bedded halite is formed is a frontier of evaporite sedimentology. Facies studies, supplemented by geochemical data, define an evaporite shelf depositional environment for the halite of the San Andres Formation of the Palo Duro Basin, Texas Panhandle, that is significantly different from modern and previously described ancient halite-precipitating environments such as playas, salinas, sabkhas, and barred basins. A coastal palaeoenvironmental setting for the San Andres halite is defined by its facies position between normal marine-shelf carbonates and aeolian deposits. The San Andres brine pool extended over more than 10 000 km² but was very shallow. Perennial brine-pool conditions (thick sequences of halite) alternated with ephemeral brine-pool conditions (halite, haloturbated mudstone-halite, mudstone interbeds, and microkarst). The depositional sequence in the perennial brine pool includes (1) flooding and minor dissolution of previously deposited halite, (2) precipitation of a thin lamina of gypsum, and (3) evaporation and precipitation of halite. Bottom-growth forms of halite, including chevrons and vertically elongated crystals, are well preserved. Cumulates of foundered, floating crystals and rafts were probably abundant but have been almost completely recrystallized. Mudstone interbeds in halite and microkarst features cut into bedded halite record the episodic interruption of brine-pool deposition and the establishment of subaerial conditions. Vertically elongated karst pits originate at the palaeosurfaces, cross-cut primary brine-pool fabrics, and are filled with geopetal sediment and coarse halite cement. Mudstone interbeds and mixtures of mudstone and halite have been haloturbated by the alternating growth and dissolution of halite reflecting conditions of fluctuating salinity. The geochemistry of halite from both ephemeral and perennial brine-pool environments reflects the frequent influx of marine brine, indicating that communication with the marine environments to the south was ‘good’ considering that restriction was sufficient to precipitate halite.     

Sequence stratigraphy of a carbonate-evaporite succession (Zechstein 1, Hessian Basin, Germany)

The evaporitic Hessian Zechstein Basin is a sub‐basin of the Southern Zechstein Basin, situated at its southern margin. Twelve facies groups were identified in the Zechstein Limestone and Lower Werra Anhydrite in order to better understand the sequence‐stratigraphic evolution of this sub‐basin, which contains economically important potassium salts. Four different paleogeographic depositional areas were recognized based on the regional distribution of facies. Siliciclastic‐carbonate, carbonate, carbonate‐evaporite and evaporite shallowing‐upward successions are developed. These allow the establishment of parasequences and sequences, as well as correlation throughout the Hessian Basin and into the Southern Zechstein Basin. Two depositional sequences are distinguished, Zechstein sequence 1 and Zechstein sequence 2. The former comprises the succession from the Variscan basement up to the lowermost part of the Werra Anhydrite, including the Kupferschiefer as part of the transgressive systems tract. The highstand systems tract is defined by the Zechstein Limestone, in which two parasequences are developed. In large parts of the Hessian Basin, Zechstein sequence 1 is capped by a karstic, subaerial exposure surface, interpreted as recording a type‐1 sequence boundary that formed during a distinct brine level fall. Low‐lying central areas (Central Hessian Sub‐basin, Werra Sub‐basin), however, were not exposed and show a correlative conformity. Topography was minimal at the end of sequence 1. Widely developed perilittoral, sabkha and salina shallowing‐upward successions indicate a renewed rise of brine level (interpreted as a transgressive systems tract), because of inflow of preconcentrated brines from the Southern Zechstein Basin to the north. This marks the initiation of Zechstein sequence 2, which comprises most of the Lower Werra Anhydrite. In the Central Hessian Sub‐basin, situated proximal to the brine inflow and on the ridges within the Hessian Basin, physico‐chemical conditions were well suited for sulphate precipitation to form a thick cyclic succession. It consists of four parasequences that completely filled the increased accommodation space. In contrast, only minor sulphate accumulation occurred in the Werra Sub‐basin, situated further southwards and distal to the inflow. As a result of substantially different sulphate precipitation rates during increased accommodation, water depth in the region became more variable. The Werra Sub‐basin, characterized by very low sedimentation rates, became increasingly deeper through time, trapping dense halite brines and precipitating rock salt deposits (Werra Halite). This ‘self‐organization’ model for an evaporitic basin, in which depositional relief evolves with sedimentation and relief is filled by evaporite thereafter, contradicts earlier interpretations, that call upon the existence of a tectonic depression in the Werra area, which controlled sedimentation from the beginning of the Zechstein.     

An Upper Aptian saline pan/lake system from the Brazilian equatorial margin: integration of facies and isotopes

Facies and isotope (Sr and S) data were combined in order to discuss the genesis and palaeohydrology of an Upper Aptian evaporite succession formed during the initial development of an intra-continental rift from northern Brazil. Comparison of facies distribution between two investigated areas shows: (i) stable, well-stratified and hypersaline lakes with periods of anoxia and closure in the eastern margin of the basin, where there was evaporite precipitation only in central lake environments; and (ii) more ephemeral conditions in the eastern margin of the basin, where a saline pan complex developed and evaporite precipitation took place mainly in marginal salinas and surrounding mudflats. In both areas, expansion/contraction cycles developed as sedimentation took place, accompanied by a decrease and then an increase in ⁸⁷Sr/⁸⁶Sr- and δ³⁴S-isotope values. This, combined with the wide distribution of Sr- and S-isotope data within individual depositional cycles, as well as petrographic and scanning electronic microscopic (SEM) images, led to the conclusion that diagenesis was not enough to obscure the primary geochemical signature. A non-marine brine source is suggested by ⁸⁷Sr/⁸⁶Sr ratios between 0·707824 and 0·709280, which are higher than those from Upper Aptian sea water (i.e. between 0·70720 and 0·70735). The δ³⁴S value varies from 16·12 to 17·89‰ in the eastern margin of the basin, which is in disagreement with Upper Aptian marine values (13 to 16‰). Both geochemical tracers were influenced by facies characteristics, and thus a model is provided, where ⁸⁷Sr/⁸⁶Sr values respond to changes in expansion and contraction episodes of saline pan/lake systems.     

罗布泊盐湖富钾卤水成因再探讨——碎屑层卤水蒸发实验分析

罗布泊盐湖钙芒硝岩孔隙中蕴藏有超大型规模的卤水钾矿,富钾卤水成因一直备受关注。罗北凹地从统一的罗布泊大湖区中分隔出来后,成盐过程中其湖水仍以南部大湖的补给为主,罗北凹地卤水化学演化与"大耳朵"湖水密切相关。"大耳朵"湖区含石膏碎屑层普遍储藏有卤水,应该是罗北凹地盐湖的"源卤水",钾离子(ρ(K~+)为3.12 g/L左右)已初步富集,平均矿化度为198.83 g/L。为了查明该卤水的化学演化趋势及析盐序列,笔者于2009年、2010年两次采集了大量卤水样品,分别进行室内等温蒸发和自然蒸发实验。蒸发实验结果表明:随着卤水浓缩首先析出(硬)石膏,随后析出大量石盐,最后出现少量钾石盐和光卤石,与EQL/EVP卤水蒸发模型模拟结果相似。将碎屑层卤水蒸发过程中化学组成变化与罗北凹地卤水进行对比,结果显示罗布泊古湖水蒸发至石膏沉积之后,在罗北凹地水化学组成明显发生变化,没有大量石盐沉积,而以钙芒硝沉积为主。推测应是受到深部"富钙水"的持续补给,而"大耳朵"湖起到"预备盆地"的作用,罗布泊古湖水经"大耳朵"湖蒸发浓缩后,钾离子得到初步富集,在流入罗北凹地后与深部"富钙"水混合,强烈蒸发浓缩,大量钙芒硝矿物析出,最后形成富钾卤水。     

A depositional model for the terminal Neoproterozoic–Early Cambrian Ara Group evaporites in south Oman

Abstract Six evaporite–carbonate sequences are recognized in the terminal Neoproterozoic–Early Cambrian Ara Group in the subsurface of Oman. Individual sequences consist of a lower, evaporitic part that formed mainly during a lowstand systems tract. Overlying platform carbonates contain minor amounts of evaporites and represent transgressive and highstand systems tracts. Detailed sedimentological and geochemical investigation of the evaporites allowed reconstruction of the depositional environment, source of brines and basin evolution. At the beginning of the evaporative phase (prograding succession), a shallow-water carbonate ramp gradually evolved into a series of shallow sulphate and halite salinas. Minor amounts of highly soluble salts locally record the last stage of basin desiccation. This gradual increase in salinity contrasts sharply with the ensuing retrograding succession in which two corrosion surfaces separate shallow-water halite from shallow-water sulphate, and shallow-water sulphate from relatively deeper water carbonate respectively. These surfaces record repeated flooding of the basin, dissolution of evaporites and stepwise reduction in salinity. Final flooding led to submergence of the basin and the establishment of an open-water carbonate ramp. Marine fossils in carbonates and bromine geochemistry of halite indicate a dominantly marine origin for the brines. The Ara Group sequences represent a time of relatively stable arid climate in a tectonically active basin. Strong subsidence allowed accommodation of evaporites with a cumulative thickness of several kilometres, while tectonic barriers simultaneously provided the required restricted conditions. Subsidence allowed evaporites to blanket basinal and platform areas. The study suggests a deep-basin/shallow-water model for the evaporites.     

四川盆地海相三叠系硬石膏和盐卤水的硫同位素组成及意义

四川盆地下、中三叠统硬石膏和盐卤水广布，通过对采集于不同地段不同层位各具代表性的硬石膏、石膏和盐卤水的２４４件样品的分析，可见其同层位硫同位素组成稳定，δ３４Ｓ自下而上具阶梯状递减轻化的趋势，与已知全球海相三叠系硫同位素组成有明显差异。这种硫同位素分布规律对地层划分和对比、蒸发岩形成环境的判断、研究卤水产层和成因、掌握蒸发岩咸化发展方向及预测找钾工作等的意义不容忽视。     

Strontium isotope composition of Middle Miocene primary gypsum (Badenian of the Polish Carpathian Foredeep Basin): evidence for continual non‐marine inflow of radiogenic strontium into evaporite basin

Strontium isotope compositions of ancient sulphate deposits not only provide chemostratigraphic information but also offer insight into the system in which the evaporites precipitated. Primary gypsum from two Middle Miocene (Badenian) sections in southern Poland shows steadily higher ⁸⁷Sr/⁸⁶Sr ratios than those expected from a marine‐derived formation. The ratios are interpreted as the result of increasing inflow into the basin at the time of gypsum precipitation. Palaeogeographic reconstructions suggest that riverine runoff sources were situated in the West and East European platforms (to the north and east, respectively) and the Carpathians (to the south), which are mostly composed of Mesozoic sedimentary rocks; their dissolution cannot be responsible for the higher ⁸⁷Sr/⁸⁶Sr ratios recorded. We conclude that Archaean and Palaeoproterozoic igneous and supracrustal rocks of the Ukrainian Shield were the source of the higher ⁸⁷Sr/⁸⁶Sr ratios recorded in the Badenian primary gypsum. A distinctive decreasing trend of ⁸⁷Sr/⁸⁶Sr ratios from western Ukraine to southern Poland is explained by a consistent direction of brine inflow during gypsum crystallization (typical cyclonic circulation controlled by the Coriolis effect).     

Sedimentological characteristics and facies of the evaporite-bearing Kirmir Formation (Neogene), Beypazari Basin, central Anatolia, Turkey

A thick sedimentary sequence comprising fluvial, lacustrine and volcano-sedimentary rocks is present in the Neogene Beypazari Basin, central Anatolia. These units display considerable lateral facies variation and interfinger with alkaline volcanic rocks along the north-eastern margin of the basin. The uppermost Miocene Kirmir Formation contains numerous evaporite horizons. The evaporite sequence is up to 250 m thick and may be divided into four lithofacies. In ascending stratigraphical order these are: (1) gypsiferous claystone facies, (2) thenardite-glauberite facies, (3) laminar gypsum facies and (4) crystalline gypsum facies. These facies interfinger with one another laterally along a section from the margins to central parts of the basin. The lithological and sedimentological features of the Kirmir Formation indicate fluvial, saline playa mudflat, hypersaline ephemeral playa lake and very shallow subaqueous playa lake depositional environments, which probably were influenced by alternating semi-arid and evaporative conditions.     

Deep to shallow lacustrine evaporites in the Libros Gypsum (southern Teruel Basin, Miocene, NE Spain): an occurrence of pelletal gypsum rhythmites

ABSTRACT A number of non‐marine evaporite units composed of primary gypsum were deposited in saline lakes that developed in the southern Teruel Basin (NE Spain) during the Miocene. In the basin depocentre, a continuum of lacustrine evaporite lithofacies influenced by the activity of organisms is displayed. The Libros Gypsum was deposited in a deep lake, in which water stratification became unstable with progressive shoaling. Rhythmites, composed of laminae of pelletal gypsum and laminae of very fine lenticular gypsum crystals mixed with siliceous microorganisms, formed in addition to gypsum turbidites, intraformational gypsum breccias and slump structures. The pelletal laminae originated from the faecal activity of animals (crustaceans?) ingesting gypsum crystallites in the lake water during episodes of maximum evaporation, whereas the laminae of very fine lenticular gypsum mixed with microorganisms accumulated during episodes of relative dilution. In the wide marginal zones of the basin, the Libros Gypsum unit consists of massive to thin‐bedded bioturbated gypsum and thin‐bedded clotted gypsum, which formed in intermediate to very shallow (palustrine) water depths. The bioturbated gypsum lithofacies were produced by the action of diverse organisms, presumably worms and coleopterans, and chironomid larvae to a lesser extent; the massive lithofacies precipitated in very shallow water; and the thin‐bedded lithofacies formed in shallow to deeper settings. The thin‐bedded clotted gypsum is a relatively deep facies that may have diverse origins (e.g. bioturbation, compaction, disruption of soft sediments and early diagenesis). There is a well‐developed metre‐scale cyclicity in the marginal lake sequences, which is not observed in the inner lake deposits. This suggests a depth control in the various lacustrine subenvironments to record cyclic evaporitic processes. The isotopic composition of the gypsum indicates early sulphate‐reducing bacterial activity in the bottom of the lake and suggests that the sulphate was derived from the chemical recycling of Triassic evaporites of the country rocks.     

A barred-basin marine evaporite in the Upper Proterozoic of the Amadeus Basin, central Australia

The Ringwood evaporite is part of the 900 m.y. old Bitter Springs Formation, a warm-water shallow-marine sequence of stromatolitic dolomite and limestone, microfossiliferous chert, red beds, quartzite, and evaporites. The evaporite at Ringwood comprises two parts: (i) a lower 127 m characterized by brecciated pyritic bituminous dolomite, together with smaller amounts of dolomite-gypsum breccia, friable chloritic dololutite, coarsely crystalline anhydrite, and satin-spar gypsum; and (ii) an upper 133 m which is similar except that bituminous dolomite forms only one bed, and the characteristic rock-type is dolomite-gypsum breccia. The evaporite is overlain by limestone breccia and massive stromatolitic limestone, interpreted as an algal reef. Gypsum is secondary after anhydrite, and the ratio of gypsum to anhydrite increases upwards. The evaporite shows none of the features of a sabkha or desiccated deep ocean basin deposit, and instead is interpreted as the filling of a barred basin which was cut off from the ocean by growth of an algal barrier reef. As circulation became restricted, bituminous dolomite deposited in the lagoon behind the reef, together with pyrite from the destruction by anaerobic bacteria of algal debris derived from the reef. With continued evaporation, brine concentration increased and gypsum precipitated. Occasional dust storms contributed wind-blown clay to the deposit. The barrier reef transgressed diachronously across the evaporite lagoon, and was eventually drowned when normal marine conditions became established. Burial of the evaporite to about 7000 m beneath the succeeding sediments of the Amadeus Basin converted gypsum to anhydrite, and formed chlorite by reaction of clay with dolomite. Late Palaeozoic tectonism folded and brecciated the rocks, and was followed by erosion which eventually exposed the evaporite to ingress of meteoric water. Hydration of anhydrite to gypsum ensued, the reaction becoming less complete with increasing depth from the ground surface.     

Marine-like potash evaporite formation on a continental playa: case study from Chott el Djerid, southern Tunisia

An exceptional flood in January 1990 led to the formation of a large ephemeral lake on the Chott el Djerid, a salt playa in southern Tunisia. Repeated observations made during 1990 show that the ephemeral lake underwent four evolutionary stages: (1) initial flooding, (2) evaporative concentration of lake waters, (3) the movement of concentrated brine pools over the playa surface as a result of wind action, and (4) total desiccation of the lake by September 1990. During all four stages the brine chemistry of the lake was monitored. Water inflow into the Chott el Djerid basin was found to have a consistent Ca-SO₄-Cl-rich and HCO₃-CO₃-poor chemistry, reflecting the recycling of homogeneous assemblages of Cretaceous, Mio—Pliocene and Quaternary evaporites within the catchment. As the ephemeral lake shrank, these waters produced an Na-Mg-K-Cl-SO₄ brine which was similar to modern sea water. Mineral saturation data show that, during the desiccation of the lake, saturation with respect to both gypsum and halite was achieved and that the most concentrated brines were ultimately saturated with respect to potash phases. After the desiccation of the lake the main mineral phases found on the Chott included gypsum and halite. In addition, ephemeral deposits of carnallite (observed as carnallitite,3KMgCl_3·6H₂0 + NaCl) were found. This assemblage is that which would be expected to form if the waters had undergone salt norm evaporation at 1 bar pressure at 25°C (SNORM) in the evaporation model proposed by Jones and Bodine (1987). The nature of both the brine chemistry and evaporite mineralogy provides a new and rare example of marine-like potash-bearing evaporites being formed in a contemporary continental playa.     

Algal crusts, autochthonous and clastic gypsum in a cannibalistic evaporite basin: a case history from the Messinian of Northern Apennines

The Messinian Vena del Gesso Basin in the Northern Apennines is filled by very thick (up to 35 m) beds of coarse crystalline gypsum (selenite) associated with thinner carbonate and shaly (euxinic) intercalations. The conventional Usiglio model of salt fractionation does not apply to this evaporitic sequence for the following reasons: carbonate which underlies gypsum is not evaporitic but algal in origin; most gypsum did not precipitate from surface brines but at and below a sediment-water interface occupied by algal mats; a significant portion (10–80%) of gypsum beds is composed of redeposited selenite which was removed from the margins and transported toward the centre of the basin by slope-controlled currents and gravity flows (debris flows). We call this process cannibalistic because of its intraformational character (connected with evaporative fall of water level) and volumetric importance. A recurrent vertical pattern of six main facies (euxinic to gypsum fanglo-merates) is interpreted as a bathymetric, regressive cycle controlled by both sedi-mentological and tectonic-eustatic factors. The inferred environmental setting is a residual turbidite trough (Marnoso-arenacea) evolving abruptly toward lagoonal conditions and filled up to sea level by evaporitic and mechanical (mostly fluvial) processes. Repeated inundations of restricted-marine water started the depositional cycle thirteen or fourteen times.     

The hydrological setting, occurrence and significance of gypsum in late Quaternary salt lakes in South Australia

Well exposed, often laminated gypsum sequences occur in many Quarternary salt lakes in southern South Australia. The gypsum in the salt lakes is classified by increasing grain size into gypsite, gypsarenite and selenite. The salt lakes are classified by age and hydrological setting into coastal salinas which are Holocene sea-water fed groundwater lakes, and continental playas which are late Pleistocene endorheic basins. A study of the relationships between coastal salina hydrology and the associated gypsum deposition has shown the different types of gypsum form under distinct hydrological regimes. As the hydrology above a coastal salina depositional surface changes through time so does the type of gypsum deposited. Application of a gypsum depositional model derived from a study of the coastal salina gypsum to those portions of a continental playa gypsum unit where deposition is no longer occurring confirms the applicability of the model to non-salina gypsum deposits.     

上扬子区(四川盆地)寒武系的含盐性与地质背景

据记载,分布于上扬子区寒武系的石膏岩仅有零星资料。如今,大量蒸发岩如溶蚀角砾岩、硬石膏、石盐岩及富钾卤水等已被发现。沉积相经历了从盆地相、台地相到蒸发岩相的演化过程。在中、下寒武统中找到海退沉积序列。古构造-古地理背景是蒸发岩沉积的重要控矿条件之一。周边板块运动及塑性基底的褶皱,导致台缘隆起及台内坳陷的形成。岩相古地理图展示从碳酸盐、硫酸盐到氯化物盐类的“泪滴式”沉积相带。蒸发岩沉积于台缘隆起及礁生长进入堰塞潟湖至盐湖阶段。在稳定坳陷区沉积盆地中蒸发岩系发育;石盐岩较厚,其溴氯比值为0.2—0.4;古气候炎热、干燥;在蒸发岩体周围有沉积(封层)水及溶滤水,其含钾(K~+)量为0.10—4.76g/L;水文地球化学比值(如钾氯比值、钾盐比值及钾溴比值等)指示含钾异常;盐湖浓缩卤水达到氯化物盐类沉积阶段及相应的构造封闭程度;含盐地质标志广泛分布等等。鉴于上述,估计该区可能具备钾盐成矿条件。然而目的层埋藏太深,因此笔者建议,应在浅埋部位进行有效的成矿预测,为普查指出远景区。