Sulphate–borate relations in an evaporitic lacustrine environment: the Sultançayir Gypsum (Miocene, western Anatolia)

Calcium-borates, mainly pandermite (priceite) and howlite, but also bakerite and colemanite, are intercalated within the Sultançayir Gypsum (Miocene, Sultançayir Basin, western Anatolia). This lacustrine unit, represented by secondary gypsum in outcrop, is characterized by: (1) a clear facies distribution of depocentral laminated lithofacies and debris-flow deposits, a wide marginal zone of sabkha deposits, and at least one selenitic shoal located toward the basin margin; (2) evaporitic cycles displaying a shallowing-upward trend; and (3) a diagenetic evolution of primary gypsum to (burial) anhydrite followed by its final re-hydration. The calcium borates precipitated only in the depocentre of the lake and were partly affected by synsedimentary reworking, indicating that they formed during very early diagenesis. The lithofacies, which are made up of a host gypsum (finely laminated) and borates (nodules, irregular masses and discontinuous bands; also fine laminations), indicate that the borates grew interstitially because of the inflow and mixing of borate-rich solutions with basinal brines. Borate growth displaced and replaced primary gypsum beneath a relatively deep depositional floor. Borate formation as free precipitates was much less common. The anhydritization of primary gypsum took place during early to late diagenesis (burial <250 m deep). This process also resulted in partial replacement of pandermite and accompanying borates (bakerite and howlite) as well as other early diagenetic minerals (celestite) by anhydrite. Final exhumation resulted in the replacement of anhydrite by secondary gypsum, and in the partial transformation of pandermite and howlite into secondary calcite.     

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.     

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.     

Meganodular anhydritization: a new mechanism of gypsum to anhydrite conversion (Palaeogene–Neogene,Ebro Basin,North‐east Spain)

A number of Palaeogene to Early Neogene gypsum units are located along the southern margins of the Ebro Basin (North‐east Spain). These marginal units, of Eocene to Lower Miocene age, formed and accumulated deposits of Ca sulphates (gypsum and anhydrite) in small, shallow saline lakes of low ionic concentration. The lakes were fed mainly by ground water from deep regional aquifers whose recharge areas were located in the mountain chains bounding the basin, and these aquifers recycled and delivered Ca sulphate and Na chloride from Mesozoic evaporites (Triassic and Lower Jurassic). In outcrop, the marginal sulphate units are largely secondary gypsum after anhydrite and exhibit meganodules (from 0·5 to >5 m across) and large irregular masses. In the sub‐surface these meganodules and masses are mostly made of anhydrite, which replaced the original primary gypsum. The isotopic composition (11·1 to 17·4‰ for δ¹⁸O_VSMOW; 10·7 to 15·3‰ for δ³⁴S_VCDT) of secondary gypsum in this meganodular facies indicates that the precursor anhydrite derived from in situ replacement of an initial primary gypsum. As a result of ascending circulation of deep regional fluid flows through the gypsum units near the basin margins, the gypsum was partly altered to anhydrite within burial conditions from shallow to moderate depths (from some metres to a few hundred metres?). At such depths, the temperatures and solute contents of these regional flows exceeded those of the ground water today. These palaeoflows became anhydritizing solutions and partly altered the subsiding gypsum units before they became totally transformed by deep burial anhydritization. The characteristics of the meganodular anhydritization (for example, size and geometry of the meganodules and irregular masses, spatial arrangement, relations with the associated lithologies and the depositional cycles, presence of an enterolithic vein complex and palaeogeographic distribution) are compared with those of the anhydritization generated both in a sabkha setting or under deep burial conditions, and a number of fundamental differences are highlighted.     

Sedimentology of the Cretaceous Maha Sarakham evaporites in the Khorat Plateau of northeastern Thailand

Evaporites of the Cretaceous to early Tertiary Maha Sarakham Formation on the Khorat Plateau of southeast Asia (Thailand and Laos) are composed of three depositional members that each include evaporitic successions, each overlain by non-marine clastic red beds, and are present in both the Khorat and the Sakon Nakhon sub-basins. These two basins are presently separated by the northwest-trending Phu Phan anticline. The thickness of the formation averages 250 m but is up to 1.1 km thick in some areas. In both basins it thickens towards the basin centre suggesting differential basin subsidence preceding or during sedimentation. The stratigraphy, lithological character and mineralogy of the evaporites and clastics are identical in both basins suggesting that they were probably connected during deposition. Evaporites include thick successions of halite, anhydrite and a considerable accumulation of potassic minerals (sylvite and carnallite) but contain some tachyhydrite, and minor amounts of borates. During the deposition of halite the basin was subjected to repeated inflow of fresher marine water that resulted in the formation of anhydrite marker beds. Sedimentary facies and textures of both halite and anhydrite suggest deposition in a shallow saline-pan environment. Many halite beds, however, contain a curious `sieve-like' fabric marked by skeletal anhydrite outlines of gypsum precursor crystals and are the product of early diagenetic replacement by halite of primary shallow-water gypsum. The δ³⁴S isotopic values obtained from different types of anhydrite interbedded with halite range from 14.3‰ to 17.0‰ (CDT), suggesting a marine origin for this sulphate. Bromine concentration in the halite of the Lower Member begins around 70 ppm and systematically increases upward to 400 ppm below the potash-rich zone, also suggesting evaporation of largely marine waters. In the Middle Member the initial concentration of bromine in halite is 200 ppm, rising to 450 ppm in the upper part of this member. The bromine concentration in the Upper Member exhibits uniform upward increase and ranges from 200 to 300 ppm. The presence of tachyhydrite in association with the potassic salts was probably the result of: (1) the large volumes of halite replacement of gypsum, on a bed by bed basis, releasing calcium back into the restricted waters of the basin; and (2) early hydrothermal input of calcium chloride-rich waters. The borates associated with potash-rich beds likely resulted from erosion and influx of water from surrounding granitic terrains; however, hydrothermal influx is also possible. Interbedded with the evaporites are non-marine red beds that are also evaporative, with displacive anhydrite nodules and beds and considerable amounts of displacive halite. The δ³⁴S isotopic values of this anhydrite have non-marine values, ranging from 6.4‰ to 10.9‰ (CDT). These data indicate that the Khorat and Sakhon Nakhon basins underwent periods of marine influx due to relative world sea-level rise but were sporadically isolated from the world ocean.     

The origin and significance of groundwater-seepage gypsum from Bristol Dry Lake, California, USA

Gypsum and anhydrite fabrics observed in trenches and deep (500 m) cores from Bristol Dry Lake, California, USA, exhibit a vertical alignment of crystals similar to the fabric seen in bottom-nucleated brine pond gypsum. However, geochemical and sedimentological evidence indicate that the gypsum formed in Bristol Dry Lake precipitated displacively within the sediment where groundwater saturated with respect to gypsum recharges around the playa margin (groundwater-seepage gypsum). Evidence for displacive growth of gypsum is: (i) the geometry of the deposit, (ii) stable isotopic data and the water chemistry of the brine, and (iii) inclusions of matrix which follow twin planes and completely surround crystals as they grow. The bulk of the gypsum precipitated in the playa occurs around the edges of the playa in the playamargin facies and completely rings the lake. Sulphate concentrations in the groundwater increase toward the gypsum zone in the playa margin. Basinward of this zone, sulphate concentrations decrease sharply to trace element levels in the basin centre brine. Authigenic gypsum is rare in the centre of the playa. Stable (δ¹⁸O values measured for gypsum waters of crystallization (GWC) are similar to the values calculated for groundwater in the playa margin and alluvial fan sediments (?– 6%0), whereas measured brine δ¹⁸O values range from + 0·5 to + 3·7%0. Deuterium values measured for groundwater are ?– 70%0, GWC are ?– 60 to – 65%0 and brine values are ?– 57%0. The geometry of the deposit and the chemical data suggest that the water precipitating the gypsum is more closely associated with the groundwater than the brine. However, some mixing between groundwater and brine is likely. Within 100 m of the surface, the gypsum dehydrates to anhydrite, although the same vertically aligned fabric is retained through the diagenetic process. The similarity of displacive vertically aligned gypsum and anhydrite fabrics seen in Bristol Dry Lake to subaqueously deposited gypsum in modern brine ponds indicates that the criteria used to define subaqueous fabrics must be better constrained.     

Using sedimentology to address the marine or continental origin of the Permian Hutchinson Salt Member of Kansas

The Permian Hutchinson Salt Member of the Wellington Formation of the Sumner Group of Kansas (USA) has multiple scientific and industrial uses. Although this member is highly utilized, there has not been a sedimentological study on these rocks in over 50 years, and no study has investigated the full thickness of this member. Past publications have inferred a marine origin as the depositional environment. Here, this marine interpretation is challenged. The goals of this study are to fully document sedimentological and stratigraphic characteristics of the Permian Hutchinson Salt Member in the Atomic Energy Commission Test Hole 2 core from Rice County, Kansas. This study documents colour, mineralogy, sedimentary textures, sedimentary structures, diagenetic features and stratigraphic contacts in core slab and thin sections. The Hutchinson Salt Member is composed of five lithologies: bedded halite, siliciclastic mudstone, displacive halite, bedded gypsum/anhydrite and displacive gypsum/anhydrite. These lithologies formed in shallow surface brines and mudflats that underwent periods of flooding, evapoconcentration and desiccation. Of note are the paucity of carbonates, lack of marine-diagnostic fossils, absence of characteristic marine minerals and lithofacies, and the stratigraphic context of the Hutchinson with associated continental deposits. The Hutchinson Salt Member was most likely deposited in an arid continental setting. This new interpretation offers a refined view of Pangaea during the middle Permian time.     

Extreme aridity prior to lake expansion deciphered from facies evolution in the Miocene Ili Basin,south‐east Kazakhstan

Central Asia witnessed progressive aridification during the Miocene, commonly related to mountain uplift, the Paratethys retreat and global climate cooling. However, the formation of Miocene lakes in Central Asia seems to oppose drier conditions, suggesting that the precise timing, extent and forcing of the aridification is still not well constrained. This study presents a facies model for the alluvial–lacustrine part of the Middle to Late Miocene of the Ili Basin, obtained from two successions. The model enables the semi‐quantitative assessment of regional water level and salinity, and characterizes the control of water level on evaporite formation and diagenesis. Both the proximal Kendyrlisai and the distal Aktau successions show an overall increase in water availability from dry mudflat deposits to lacustrine sedimentation with a transitional playa phase. Increasing evaporation rates outpaced the water supply and caused groundwater salinization. Subsequent lake expansion coincided with a basin‐wide desalinization and required a shift to a positive water budget. A climatic control of the hydrological evolution is inferred due to abrupt salinization and a minor tectonic influence. The long‐term water accumulation is probably related to the hydrological closure of the basin in the early Middle Miocene (15·3 Ma). Starting at 14·3 Ma, the step‐wise salinization occurred simultaneously with the global cooling of the Miocene Climate Transition. The Miocene Climate Transition led to extreme aridity in the Ili Basin, highlighted by the early diagenetic formation of displacive anhydrite in the basin centre. The expansion of the freshwater lake (12·7 to 11·5 Ma) was possibly promoted by lower evaporation rates due to decreasing air temperatures in the Ili Basin after the Miocene Climate Transition. The extreme aridity in the Ili Basin is interpreted as a continental counterpart to the Badenian Salinity Crisis in the Central Paratethys. This emphasizes the role of atmospheric forcing on evaporite sedimentation across Eurasia during the Middle Miocene.     

Environmental and sequence stratigraphic implications of anhydrite textures: A case from the Lower Triassic of the Central Persian Gulf

The Lower Triassic Kangan Formation in the Persian Gulf (South Pars Gas Field) and its adjacent areas are composed of carbonate–evaporite sequences. These sediments were deposited in a shallow marine homoclinal ramp. Study of the anhydrite-bearing intervals shows various structures and textures. The anhydrite structures are mainly bedded, massive, chicken-wire and nodular type and the main textures are felted, sparse crystal, needle shape, lath shape, equant and fibrous. Pervasive and poikilotopic cement together with replacement and porphyroblastic gypsum are accounted as the most common diagenetic features in anhydrite. Evaluation of anhydrite occurrences and features support both primary and secondary formations. The nodular to chicken-wire anhydrite formed under synsedimentary sabkha conditions, whereas anhydrite cements occurred during the late stages of diagenesis (shallow burial stage). Massive to bedded anhydrite could have been formed under subaqueous conditions or originated by coalescing and continued growth of anhydrite nodules in the sabkha zone. Anhydrite fabrics impose a significant control on the reservoir quality of the Kangan carbonates at the South Pars Gas Field. Thick massive and bedded anhydrite could have been formed as an intraformational seals and anhydrite cements occluded pore spaces and reduced the poroperm values. The sequence stratigraphic analysis revealed two depositional sequences in the studied intervals, which are composed of TST and HST. Investigation of anhydrite throughout depositional sequences indicates a change in the content and style of anhydrite texture. Anhydrite content (volume) decreases upward through transgressive system tract (sea-level rise) whereas, it enhances during highstand system tract (sea-level fall). Pervasive and poikilotopic anhydrite cements together with replacement by anhydrite are prevalent features during transgressive and early highstand system tract. At the late HST, with a progradational stacking pattern, anhydrite value increases and felted, radial, equant, crystalline and mosaic texture are the most common anhydrite fabrics. Sequence boundaries that indicate maximum sea level fall and exposure of successions are marked by the broad anhydrite deposits with massive to bedded and chicken-wire structures and various textures that located in late HST package. There is an unambiguous relationship between the microfacies associations, the evaporite textures, and the sea-level fluctuations. This relationship could lead to a predictable pattern that can be of use as a general guide for the sequence stratigraphic interpretations in the area.     

Neogene evaporites in desert volcanic environments: Atacama Desert, northern Chile

The Upper Miocene and Pliocene evaporite deposits of the Atacama Desert of northern Chile (Hilaricos and Soledad Formations) are among the few non‐marine evaporites in which aridity not only formed the deposits, but has also preserved them almost unaltered under near‐surface conditions. These deposits are largely composed of displacive Ca sulphate and halite together with minor amounts of glauberite, thenardite and polyhalite. However, at the base and top of these deposits, there are also beds of gypsum crystal pseudomorphs that originally formed as free‐growth forms within shallow brine bodies, rather than as displacive sediments. The halite is present as interstitial cement, displacive cubes and shallow‐water, bottom‐growth chevron crusts. Most of the calcium sulphate is presently anhydrite, pseudomorphous after gypsum, that was the primary depositional sulphate mineral. The secondary anhydrite formed under early diagenetic conditions after slight burial (some metres) resulting from the effect of strongly evolved pore brines. The anhydrite has been preserved without rehydration during late diagenetic and exhumation stages on account of the arid environment of the Atacama Desert. Both the Hilaricos and the Soledad Formations contain geochemical markers indicating that these Neogene evaporites had a largely non‐marine origin. Bromine content in the halite is very low (few p.p.m.), indicating neither a sedimentological relation with sea water nor the likelihood of direct recycling of prior marine halites. Moreover, the δ³⁴S of sulphates (+4·5‰ to +9‰) also reflects a non‐marine origin, with a strong volcanic influence, although some recycling of Mesozoic marine sulphates cannot be ruled out. δ³⁴S of dissolved sulphate from hot springs and streams in the area commonly displays positive values (+2‰ to +10‰). Leaching of oxidized sulphur and chlorine compounds from volcanoes and epithermal ore bodies, very common in the associated drainage areas, have been the main contribution to the accumulation of evaporites. The sedimentary and diagenetic evolution of the Hilaricos and Soledad evaporites (based on lithofacies analysis) provides information about the palaeohydrological conditions in the Central Depression of northern Chile during the Neogene. In addition, the diagenesis and exhumation history of these evaporites confirms the persistence of strongly arid conditions from Late Miocene until the present. A final phase of tectonism took place permitting the internal drainage to change and open to the sea, resulting in dissolution and removal of a significant portion of these deposits. Despite the extensive dissolution, the remaining evaporites have undergone little late exhumational hydration.     

靖边潜台西侧奥陶系马五4亚段岩相古地理特征

鄂尔多斯盆地中奥陶统马五₄亚段是靖边气田重要的天然气勘探层段,目前相关的岩相古地理图多以段和亚段为单位、以盆地为尺度,作图精度不能满足油气勘探开发的需要。以靖边潜台西侧为研究区,根据该区的古地貌特征、标志性矿物（硬）石膏的类型及其环境意义,分马五₄3、马五₄2和马五₄1三个小层开展岩相古地理工作。根据沉积背景和地层等厚图将该区中部厚度较大、地形略陡的区域解释为洼地,将洼地周边厚度较小、地形平缓的区域解释为坪。目的层段（硬）石膏有块状、球状结核和晶体等三种类型,块状硬石膏与暗色泥质藻纹层白云岩互层,代表了一种浅水水下蒸发、间或遭海水漫侵的潮上环境;球状硬石膏结核分散于浅黄色泥粉晶白云岩中,为准同生成因,代表了蒸发、偏氧化、变盐度的潮上环境;石膏晶体相对较少,多为柱状,或与球状硬石膏结核混生,代表的沉积环境与球状硬石膏结核基本相同。块状硬石膏主要分布于洼地中,为潮上带硬石膏洼地,根据硬石膏的含量进一步细分为含块状硬石膏白云岩洼地、块状硬石膏质白云岩洼地和白云质块状硬石膏洼地;球状硬石膏结核及石膏晶体主要分布于古地貌的坪中,结合其局限蒸发潮上带的背景,将其命名为球状硬石膏结核白云岩潮坪。马五₄3、马五₄2和马五₄1的岩相古地理格局基本一致,但从下向上,硬石膏洼地范围逐渐收缩,块状硬石膏的含量也逐渐下降,反映了沉积过程中水体逐渐蒸发变浅的过程。     

Evolution of late Triassic rift basin evaporites (Passaic Formation): Newark Basin, Eastern North America

The Passaic Formation of the late Triassic Newark Supergroup is 2700 m thick and was deposited in series of wide, deep to shallow lacustrine environments in the Newark rift basin (eastern North America). The Passaic Formation can be divided into lower, middle, and upper sections based on depositional structures, composition and the distribution and morphology of its evaporites. Evaporites formed as a result of syndiagenetic cementation and/or displacive processes. Evaporitive minerals now include gypsum and anhydrite, although other mineral species, such as glauberite, may have originally existed. Most of the evaporites of the Passaic Formation occur within massive red mudstone and siltstone lithologies in the form of diffuse cements, void-fillings, euhedral crystals, crystal clusters and nodules. These evaporites grew displacively within the fine siliciclastic matrix as a result of changes in the hydrochemical regimes of the rift basin. A well-developed upward increase in the amount of evaporite material is present in the Passaic Formation. This resulted from: (1) long-term, progressive increase in aridity, and (2) significant increase in evaporation surface area of the basin during its tectonic evolution. A nonmarine source for the evaporites is evident from the isotopic data. Sulphate δ³⁴S ranges from 11%. to 3.3%. CDT, while δ¹⁸O ranges from + 15.1%. to + 20.9%. SMOW, indicating derivation from early diagenetic oxidation of organic sulphur and pyrite within the organic-rich, lacustrine deposits. The ⁸⁷Sr/⁸⁶Sr ratios in sulphate are radiogenic (average 0.71211), showing the interaction of basin waters with detrital components and that the Newark Basin was isolated from the world ocean. Most of the original evaporites show evidence of diagenetic change to polycrystalline and polymineralic pseudomorphs now filled with recrystallized coarse-grained anhydrite (1–3 mm size) and low-temperature albite. Homogenization temperatures of fluid inclusions within the coarse-grained anhydrite indicate crystallization temperatures for anhydrite in the range of 150° to 280°C. Such elevated temperatures resulted from circulation of hot water in the basin. Later exhumation of these rocks caused partial to total replacement of anhydrite by gypsum in the upper part of the section. The resulting increase in volume due to hydration of anhydrite at shallow depths also emplaced non-evaporative satin-spar veins (fibrous gypsum) along bedding planes and in fractures. While the local geology of the Newark rift basin controlled the distribution of facies, the sedimentological development of the Passaic Formation evaporites resulted from the world-wide climatic aridity that prevailed during the late Triassic. because the Newark Basin sequence was only covered with about 3 km of sedimentary overburden that correspond to about 100°C and hence suggests that evaporites have experienced alteration by hot fluids. 5 As the Triassic marks the greatest evaporite formation world-wide and profound sense of parched continentality throughout the world existed before the final break-up of the Pangea, the Passaic Formation evaporites are an example of the influence of these palaeoclimatic conditions at the eastern margin of North America.     

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.     

Silicification of sulphate evaporites and their carbonate replacements in Eocene marine sediments, Tunisia: two diagenetic trends

Samples of chert nodules, diagenetic carbonates and evaporites (gypsum/anhydrite) collected from the gypsiferous limestones of the Kef Eddour Member (Ypressian‐Priabonian) near Metlaoui and Sehib (Tunisia) show selective silicification with great variety in the silicified by‐products. Based on δ¹³C values, which support an organic origin for the carbon, carbonates replaced evaporites microbially through bacterial sulphate reduction. Observations and results suggest two scenarios for chert formation that are related to the rate and timing of diagenetic carbonate replacement of the evaporites (anhydrite/gypsum). In the absence of early diagenetic carbonate phases, silica with δ¹⁸O values from +25 to +28·6‰ [standard mean ocean water (SMOW)] replaced the outer parts of anhydrite nodules at pH < 9. In contrast, pore‐fluid pH values > 9 in the innermost parts of the anhydrite nodules prevented silica precipitation. The record of this chemical barrier is preserved in the microquartz rims and geode features that formed in the inner parts of the nodules after dissolution of the anhydrite nucleus. The microbial diagenetic replacement of evaporites (bacterial sulphate reduction) by carbonates (calcite, aragonite and dolomite) favoured silica replacement of carbonates rather than evaporites. Silica, with δ¹⁸O signature of +21 to +26‰ (SMOW), replaced carbonates on a volume‐for‐volume basis, yielding a more siliceous groundmass, and accounting for 90–95% of the nodules. The relatively higher δ¹⁸O values of quartz replacing anhydrite can be explained by a diagenetic fluid in equilibrium with mixed (meteoric/marine) to marine water. The lower δ¹⁸O values of the quartz that replaced the diagenetic carbonates are ascribed to flushing by meteoric water in a later diagenetic stage. The silica supply for chert formation could be derived from the reworked bio‐siliceous deposits (diatomites) to the west of the basin [vestiges of an opal‐CT precursor undetectable by X‐ray diffraction (XRD) were revealed by δ²⁹Si magic‐angle‐spinning nuclear magnetic resonance investigations], diagenesis of the extraformational and overlying clay‐rich beds (the host limestones are clay‐poor as shown by XRD measurements), and minor volcanogenic and hydrothermal contributions during early diagenetic stages.     

Diagenetic Evolution and Formation Mechanisms of High-Quality Reservoirs under Multiple Diagenetic Environmental Constraints: An Example from the Paleogene Beach-Bar Sandstone Reservoirs in the Dongying Depression, Bohai Bay Basin

The diagenetic environment, diagenetic responses, diagenetic transformation model and formation mechanisms of high-quality reservoirs (beach-bar sandstones of the Paleogene fourth member) in the Dongying depression were studied through the analysis of fluid inclusions, thin section and burial evolution history. The diagenetic fluids of the beach-bar sandstone reservoirs evolved from early high salinity and weak alkalinity to low salinity and strong acidity, late high salinity and strong alkalinity and late low salinity and acidity, which were accompanied by two stages of oil and gas filling. The fluids at the margins of the sandbodies were continuously highly saline and strongly alkaline. The western (eastern) reservoirs experienced early open (closed), middle open, and late closed diagenetic environments during their burial history. The flow pattern was characterized by upwelling during the majority of the diagenesis (in the east, a non-circulating pattern transitioned into an upwelling current). Due to the evolution of the diagenetic fluids, the diagenetic sequence of the beach-bar reservoirs was as follows: early weak carbonate cementation; feldspar and carbonate cement dissolution and authigenic quartz cementation; late carbonate and anhydrite cementation, authigenic feldspar cementation, and late quartz dissolution; and late carbonate cementation, feldspar dissolution, and authigenic quartz cementation. The diagenetic strength during these stages varied or was absent altogether in different parts of the reservoirs. Due to the closeness of the diagenetic environment and the flow pattern of the diagenetic fluids, the diagenetic products are variably distributed in the sandstones interbedded with mudstones and in the fault blocks. The evolution of multiple alternating alkaline and acidic diagenetic environments controlled the distribution patterns of the reservoir diagenesis and reservoir space, and the reservoir quality index, RQI, increased gradually from the margins to the centers of the sandstones. The closeness of the diagenetic environment and the flow patterns of the diagenetic fluids controlled the differences in the reservoir properties among the fault blocks. With increasing distance from the oil-source faults, the RQI values in the west gradually decreased and in the east initially increased and then decreased.     

Mechanism of calcrete formation in the Lower Cretaceous (Neocomian) fluvial deposits,northeastern Iran based on petrographic,geochemical data

The Kopet-Dagh basin of northeastern Iran was formed during the Middle Triassic orogeny. From Jurassic through Miocene time, sedimentation was relatively continuous in this basin. The Shurijeh Formation (Neocomian), which consists of red bed siliciclastic sediments that were deposited in fluvial depositional settings, crops out in the southeastern part of the Kopet-Dagh basin. In addition to clastic lithofacies, non-clastic facies in the form of calcrete paleosols, were identified in this formation. The calcrete host rocks are mainly sandstone, pebbly sandstone. The calcrete in middle unit in the Shurijeh Formation consists of, from bottom to top: incipient calcrete, nodular calcrete, massive calcrete horizons. The maturity pattern of these calcrete gradationally increases from bottom to top in this unit. Lack of organo-sedimentary structure (mainly plant roots), diversity of calcite fabric, suggest that the studied calcretes have a multi-phase development: a short vadose phase followed by a long phreatic phase. These calcretes are neither pedogenic nor groundwater calcretes. Petrographic studies show that they are composed of micritic textures with a variety of calcite fabrics, microsparitic/sparitic veins, displacive, replacive fabrics, quartz, hematite grains. Cathodoluminescence images, trace elemental analysis (Fe, Mn increased, Na, Sr decreased) of calcrete samples show the effects of meteoric waters during the calcrete formation when water tables were variable. In this study, we conclude that evaporation, degassing of carbon dioxide are the two main factors in the formation of non-pedogenic or groundwater calcrete. The sources of carbonate were probably parent materials, surface waters, ground waters, eolian dusts, numerous outcrops of limestones that have been exposed in the source area during Neocomian time.     

石膏对白云岩溶解影响的实验模拟研究

表生到埋藏成岩作用的温度与压力（４０-１３０℃、常压－３０ＭＰａ）条件下，含膏与不含膏白云岩的溶解实验证明:在表生与相对浅埋藏的温压条件（低于７５℃，２０ＭＰａ）下，石膏（或硬石膏）的存在可不同程度地加速白云岩的溶解，随着实验温度和压力的升高，石膏（或硬石膏）对白云岩溶解的这种积极作用逐渐降低。在相对深埋藏的温压条件（高于７５℃、２０ＭＰａ）下，石膏（或硬石膏）的存在显著阻止白云岩的溶解，随着实验温度和压力的继续升高，石膏（或硬石膏）对白云岩溶解的这种消极作用也逐渐增加。从实验的这种结果可以预测，在近地表条件下和埋藏成岩作用的早期阶段，由溶解作用造成的含膏白云岩地层的次生孔隙将比不含膏的白云岩地层更为发育，因而在经历了古风化作用的地层中，含膏白云岩层更易形成良好的储层；与之相反，在相对高温高压的深埋藏成岩阶段，不含膏的白云岩地层中将更容易因酸性水的溶解作用而形成次生孔隙。因而在非蒸发沉积环境中形成的白云岩体（如正常海沉积环境的灰岩中的白云岩透镜体）更易因深埋藏溶蚀作用而形成良好的储层。     

Diagenesis of Barremian-Aptian platform carbonates (the Urgonian Limestone Formation of SE France): near-surface and shallow-burial diagenesis

The diagenesis of carbonate platform sediments is controlled by the original facies and mineralogy, climate, sea-level changes and burial history; these controls are clearly seen in the diagenesis of the Urgonian platform carbonates of SE France. Early diagenesis in the Urgonian platform included the precipitation of marine cements, dissolution of rudist shells and minor karstification. Diagenetic features produced during this phase were controlled by several falls in relative sea-level during the Barremian to mid-Aptian punctuating platform sedimentation, the original mineralogy of the sediment and the prevailing semi-arid/arid climate in the region at this time. Following a relative sea-level rise and further sedimentation, progressive burial of the platform led to minor compaction, followed by precipitation of coarse, equant, zoned to non-luminescent, calcite cement. This cement was cut by later stylolites, suggesting a relatively shallow-burial origin. Stable isotope (mean values - 7.94%δ¹⁸O and 0.36%δ¹³C) and trace element (mean values of Fe 334 ppm, Mn 92 ppm and Sr 213 ppm) data suggest that these cements precipitated from meteoric fluids at temperatures slightly elevated relative to depositional temperatures. A variable thickness of replacive dolomite which occurs preferentially within the shelf-margin facies of the lower part of the Urgonian post-dates mechanical fracturing and chemical compaction, but pre-dates the main phase of stylolitization. It is probable that the dolomitizing fluid was sourced by the early compaction-driven release of connate fluids held within the underlying muddy units. The burial history of these rocks suggests that calcite cementation and dolomitization took place at relatively shallow burial depths (1–1.5 km). The overall diagenetic history of the Urgonian Limestone Formation is a reflection of the pre-conditioning of the platform limestones by climate, sea level, tectonics and the shallow burial depths experienced by the platform during the later Mesozoic.     

Sedimentology of Badenian (middle Miocene) gypsum in eastern Galicia, Podolia and Bukovina (West Ukraine)

Primary gypsum is the main evaporite mineral in the middle Miocene (Badenian) of the West Ukraine. The lower part of the gypsum sequence is built of autochthonous gypsum while the upper part is composed of allochthonous gypsum that formed following a major, tectonically induced, change in basin morphology. This change resulted in the destruction of the gypsum deposited on the margins of the basin and formation of redeposition features. Autochthonous gypsum facies were deposited in two main environments: (1) giant gypsum intergrowths precipitated from highly concentrated brines; (2) very shallow subaqueous gypsum deposited in a vast brine pan. The brine pan was characterized by a facies mosaic that reflects an interplay of concentrated brines from the central part of the evaporite basin and diluted brines due to the influx of continental meteoric waters. The facies continuum, microbial gypsum - bedded selenite - massive selenite - sabre gypsum, indicates increasing salinity of the brine with time. This type of facies pattern has been established in recent salinas that are analogous to Badenian gypsum in their lateral facies changes. However, the pattern of facies distribution with respect to the open sea in the Badenian basin is opposite to that found in recent salinas. The pattern of the Badenian gypsum facies in the Ukraine indicates that facies repetition may have been related to climatically controlled salinity changes and not to depth changes, as is commonly used to explain the repetition of sulphate facies in a vertical succession.     

Diagenetic mineral development within the Upper Jurassic Haynesville-Bossier Shale,USA

Despite recent advances, diagenetic processes in fine-grained sediments are still relatively poorly understood. Key questions still to be resolved include the types of diagenetic minerals present in mudstones and the extent of element mobility in these low permeability systems. This study utilizes data from the Haynesville-Bossier Shale, USA, to analyze lithologies, discriminate authigenic phases and identify mobile elements during diagenesis. It has implications for understanding how authigenic minerals develop and the sources of those authigenic minerals in fine-grained sediments. On the basis of grain-size and mineralogy five lithologies are designated: (i) silica-rich argillaceous mudstones; (ii) argillaceous siliceous mudstones; (iii) mixed siliceous mudstones; (iv) mixed mudstones; and (v) authigenically-dominated mudstones. The diagenetic development of the Haynesville-Bossier Shale can be divided into early and late diagenesis. Ferroan and non-ferroan dolomite, framboidal pyrite and bioclast pore-filling kaolinite and calcite grain replacements and cements all formed during early diagenesis. Late diagenetic mineral phases include illite formed by the illitization of smectite, replacive and displacive chlorite, calcite-replacive albite, quartz-replacive calcite and replacive and/or displacive quartz. The presence of extensive late diagenetic mineral precipitates indicates that there was a degree of element mobility on at least the local scale. Aluminium present in albite is most likely to have resulted from the illitization of smectite. Quartz overgrowths probably resulted from illitization and the pressure dissolution at quartz silt grain boundaries. Externally, hydrothermal fluids resulting from regional-scale igneous activity appear to have played a role in the formation of chlorite and possibly albite. The work indicates that extensive mineral development and element mobility occurred during late diagenesis.