Composition of brines in halite‐hosted fluid inclusions in the Upper Ordovician,Canning Basin,Western Australia: new data on seawater chemistry

Analyses of primary and early diagenetic fluid inclusions in the halite from the Late Ordovician Mallowa Salt, Canning Basin, Western Australia indicate a Ca‐rich composition and high concentration of parent brines in the basin which were close to sylvite and carnallite precipitation. The salt‐bearing series in the sampled interval was overheated up to 62 °C. The recorded differences in gas compositions result from the input of several gas sources including dispersed organic matter in the salt series and hydrocarbon deposits in the underlying rocks. The high concentration of the brines in fluid inclusions does not allow quantitative reconstruction of the chemical composition of Late Ordovician parent seawater. Using the information from Early Cambrian and Late Silurian basins as a proxy, however, the new data indicate that Late Ordovician seawater was undoubtedly Ca‐rich and, in comparison with modern seawater, had a similar K content, considerably lower Mg content (c. 30%), approximately three times the Ca content and one‐third the SO₄ content.     

Significance of stromatolites for the environmental interpretation of the Buntsandstein (Lower Triassic) rocks

When interpreting the depositional environment of the Buntsandstein sequence, thin stromatolite layers, if present, were often overlooked or given short shrift. The present paper provides evidence of value of stromatolites for the environmental interpretation of the Buntsandstein rocks. Algal stromatolites found in western Poland occur in form of thrombolites, LLH-type structures, SH-type structures, and rarely as oncolites. Stromatolites are usually associated with oolites. Very often stromatolites show important traces of scouring and channelling action of water. Since stromatolites occurred in the zone of clastic-carbonate deposition they were covered up by continuous sheet of detrital grains. Periodic catastrophic erosion and deposition was produced by hurricanes and severe storms in the peritidal and shallow subtidal zone. It is possible to distinguish the peritidal and subtidal stromatolites. In the vicinity of stromatolites are of frequent occurrence spirorbids, conchostracs, gastropods, and rare foraminifers. Besides, spirorbids are associated with stromatolites — they constituted the initial hard substratum for the stromatolitic structures and sometimes they also occur inside stromatolites. The not-hypersaline sedimentary environment of the Buntsandstein rocks can be compared with modern environments of the Persian Gulf and the Gulf of Aqaba.     

Strontium distribution and celestite occurrence in Zechstein (Upper Permian) anhydrites of West Poland

The previous study showed that the Zechstein (Upper Permian) anhydrites have about 0.2% strontium with a remarkably small sample scatter. Our study of three lower Zechstein anhydrite units (Lower Anhydrite, Upper Anhydrite and Basal Anhydrite) from West Poland indicate that although often the Sr content is 0.1–0.2%, there are common deviations. In particular, a considerable part (28%) of the studied samples is characterized by lower values (<0.1%), and on the other hand ca. 15% of samples are Sr-enriched, and in those samples celestite was recorded. Particular anhydrite levels differ especially in the frequency of samples showing great Sr content. The greatest variation was found in the Lower Anhydrite. This agrees well with the conclusion derived from the sedimentological studies indicating that there was the greatest differentiation of depositional environments during the deposition of the Lower Anhydrite. The Sr content is a good indicator of brine concentration during the gypsum precipitation and it seems that the subsequent gypsum–anhydrite transformation itself does not affect the strontium distribution. The histograms of Sr content in the Basal Anhydrite indicate a slightly higher brine concentration than it was during the Lower Anhydrite deposition, and the latter in turn was higher than brine concentration during the Upper Anhydrite sedimentation. Celestite veins are clearly diagenetic in origin. The form of celestite occurrence and the increased strontium content (1% or more) indicate an additional source of ions that occurred outside the anhydrite series. In the case of the Lower Anhydrite, the supposed additional source of Sr was related to aragonite-to-calcite transition and squeezing of CaCl₂ brines from reefs into anhydrite series due to increased pressure. For the Basal Anhydrite this source could be related to brines derived from the Older Halite deposits.     

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).     

Stable chlorine isotope evidence for non-marine chloride in Badenian evaporites, Carpathian mountain region

Routine trace-element geochemistry suggests that components in putative marine halite evaporites may be partly of nonmarine origin, but such interpretations are commonly ambiguous. Stable chlorine isotopes may provide a less-ambiguous marker of chloride origin where δ³⁷Cl departs from the range predicted for evaporite formation from seawater. Bedded halite with primary sedimentary textures preserves original δ³⁷Cl values. Measurable change in δ³⁷Cl can be generated by incongruent dissolution of halite, but only if less than half the original halite remains. Badenian (middle Miocene) halite from the Forecarpathian and from the East Slovakian and Transcarpathian basins has a δ³⁷Cl range of – 0.2 to 0.8‰. Two phenomena cannot be explained by simple evaporation of 0.0‰ seawater. At Wieliczka, the Shaft Salt has distinctive δ³⁷Cl values (– 0.2 to 0.0‰) relative to neighbouring salt beds (0.2 to  0.6‰), requiring a large, abrupt input of brine with negative δ³⁷Cl. Halite with high (0.6 – 0.8‰) δ³⁷Cl near the base of the East Slovakian and Transcarpathian evaporites requires a large input of chloride with positive δ³⁷Cl into the basins. Expulsion of basin brine with non-0‰δ³⁷Cl into the evaporite basins may account for the nonmarine chloride sources.     

Foraminiferal changes and geochemical profiles across the Cenomanian/Turonian boundary in central and south-east Poland

Two sections of the Upper Cenomanian and Lower Turonian in central and south-east Poland were investigated for foraminifers, CaCO₃content, carbon content insoluble in HCl (C_org) and in the carbonates (C_carb), carbon and oxygen isotopic composition of bulk-rock carbonates and elemental abundances. The Cenomanian/Turonian boundary interval is characterized by the appearance of more marly facies, a δ¹³C and δ¹⁸O stable isotope anomaly, a considerable increase in C_org content and decrease in C_carb content and substantial changes in the foraminiferal assemblages. A major carbon stable isotope excursion with a shift of +2 (PDB) occurs in the lowermost Whiteinella archaeocretacea Zone. The late Cenomanian δ¹³C anomaly is associated with heavy δ¹⁸O values. The peak value of δ¹³C corresponds to the minima in P/B ratio and in diversity of foraminiferal assemblages. A late Cenomanian anoxic event is thought to be responsible for changes in foraminiferal assemblages. However, elemental abundance analyses do not show changes in the concentrations of trace elements. This may be explained by the long distance between studied area and a source of enrichment which was probably located in the western hemisphere.     

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.     

Stable chlorine isotopes in Phanerozoic evaporites

Modern seawater has a uniform δ³⁷Cl value (0.0‰), with an exception in the upper current of the Bosphorus (0.4‰). Marine halite ranging in age from Cambrian to Miocene has δ³⁷Cl values of 0.0 ± 0.9‰, with most of the data in the range 0.0 ± 0.5‰. Mean δ³⁷Cl values differ measurably between basins, with no evident relationship to basin size or to age. Smaller evaporite bodies have the largest δ³⁷Cl ranges. Potash facies halite has mean δ³⁷Cl values lower than those of halite facies salt in the East Siberia and Zechstein basins. The bulk δ³⁷Cl of bedded halite preserving sedimentary textures cannot be shifted measurably after deposition under plausible natural conditions. During the Phanerozoic, a detectable change in the δ³⁷Cl values of the oceans is unlikely as a result of Cl fluxes to and from the mantle and evaporites. In halite, the values of δ³⁷Cl that cannot be explained by fractionation occurring on crystallization are best explained by the addition of non-marine Cl with δ³⁷Cl ≠ 0.0‰ to evaporite brine.     

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.