Fluid Inclusions In Halite Research Articles

Nucleation-assisted microthermometry: A novel application to fluid inclusions in halite

Halite deposits have long been utilized for interrogating past climate conditions. Microthermometry on halite fluid inclusions has been used to determine ancient water temperatures. One notable obstacle in performing microthermometric measurements, however, is the lack of a vapor bubble in the single-phase liquid inclusions at room temperature. (Pseudo-) isochoric cooling of the inclusions to high negative pressures, far below the homogenization temperature, has commonly been needed to provoke spontaneous vapor bubble nucleation in the liquid. High internal tensile stress in soft host minerals like halite, however, may induce plastic deformation of the inclusion walls, resulting in a wide scatter of measured homogenization temperatures. Nucleation-assisted (NA) microthermometry, in contrast, employs single ultra-short laser pulses provided by a femtosecond laser to stimulate vapor bubble nucleation in metastable liquid inclusions slightly below the expected homogenization temperature. This technique allows for repeated vapor bubble nucleation in selected fluid inclusions without affecting the volumetric properties of the inclusions, and yields highly precise and accurate homogenization temperatures.In this study, we apply, for the first time, NA microthermometry to fluid inclusions in halite and we evaluate the precision and accuracy of this thermometer utilizing (i) synthetic halite crystals precipitated under controlled laboratory conditions, (ii) modern natural halite that precipitated in the 1980s in the Dead Sea, and (iii) Late Pleistocene halite samples from a sediment core from Death Valley, CA. Our results demonstrate an unprecedented accuracy and precision of the method that provides a new opportunity to reconstruct reliable quantitative temperature records from evaporite archives.

Late Paleocene paleoclimate recorded in fluid inclusion of halite in Subei basin, East China

Salt deposits are indicative of relatively extreme climate events. However, due to insufficient independent temperature proxies, paleotemperature records obtained from salt deposition are still lack. The Paleocene evaporite sequence deposited in the Hongze Depression of Subei Basin of eastern China provides an important terrestrial sediment record during this period. In this study we present total of 488 homogenization temperature (Th) data of halite fluid inclusions from drilling core with different stratigraphic depth after detailed petrological observation. The obtained Th ranged from 17.7 °C to 52.3 °C, with the mean Th value of 34.1 °C that in good agreement with the previous studies of climatic proxies. Our study shows that primary fluid inclusions of halite can serve as a robust tool to construct the ancient earth surface temperature.

The evolution of Earth's surficial Mg cycle over the past 2 billion years.

The surficial cycling of Mg is coupled with the global carbon cycle, a predominant control of Earth's climate. However, how Earth's surficial Mg cycle evolved with time has been elusive. Magnesium isotope signatures of seawater (δ26Mgsw) track the surficial Mg cycle, which could provide crucial information on the carbon cycle in Earth's history. Here, we present a reconstruction of δ26Mgsw evolution over the past 2 billion years using marine halite fluid inclusions and sedimentary dolostones. The data show that δ26Mgsw decreased, with fluctuations, by about 1.4‰ from the Paleoproterozoic to the present time. Mass balance calculations based on this δ26Mgsw record reveal a long-term decline in net dolostone burial (NDB) over the past 2 billion years, due to the decrease in dolomitization in the oceans and the increase in dolostone weathering on the continents. This underlines a previously underappreciated connection between the weathering-burial cycle of dolostone and the Earth's climate on geologic timescales.

Impact of seawater sulfate concentration on sulfur concentration and isotopic composition in calcite of two cultured benthic foraminifera

Abstract. Marine sediments can be used to reconstruct the evolution of seawater [SO42-] and δ34S over time, two key parameters that contribute to refine our understanding of the sulfur cycle and thus of Earth's redox state. δ34S evolution can be measured from carbonates, barites and sulfate evaporites. [SO42-] variations can be reconstructed using fluid inclusions in halites, a method that only allows a low-resolution record. Reconstruction of the past sulfur cycle could be improved if carbonates allowed the tracking of both seawater δ34S and [SO42-] variations in a sole, continuous sedimentary repository. However, most primary carbonates formed in the ocean are biogenic, and organisms tend to overprint the geochemical signatures of their carbonates through a combination of processes often collectively referred to as vital effects. Hence, calibrations are needed to allow seawater δ34S and [SO42-] reconstructions based on biogenic carbonates. Because foraminifera are important marine calcifiers, we opted to focus on calcite synthesized by individuals of rosalinid benthic foraminifera cultured in the laboratory under controlled conditions, with varying seawater [SO42-] (ranging from 0 to 180 mM). Our experimental design allowed us to obtain foraminiferal asexual reproduction over several generations. We measured bulk carbonate-associated sulfate (CAS) content and sulfur isotopic composition (δ34SCAS) on samples of tens to hundreds of specimens from a selection of culture media, where [SO42-] varied from 5 to 60 mM. Increasing or decreasing [SO42-] with respect to modern-day seawater concentration (28 mM) impacted foraminiferal population size dynamics and the total amount of bioprecipitated carbonate. Foraminiferal CAS concentration increased proportionally with [SO42-] concentration from 5 mM up to 28 mM and then showed a plateau from 28 to 60 mM. The existence of a threshold at 28 mM is interpreted as the result of a control on the precipitation fluid chemistry that foraminifera exert on the carbonate precipitation loci. However, at high seawater sulfate concentrations (> 40 mM) the formation of sulfate complexes with other cations may partially contribute to the non-linearity of the CAS concentration in foraminiferal tests at high increases in [SO42-]. Yet, despite the significant effect of seawater [SO42-] on foraminiferal reproduction and on CAS incorporation, the isotopic fractionation between CAS and seawater remains stable through varying seawater [SO42-]. Altogether, these results illustrate that CAS in biogenic calcite could constitute a good proxy for both seawater [SO42-] and δ34S and suggests that sulfate likely plays a role in foraminiferal biomineralization and biological activity.

Seafloor hydrothermal systems control long-term changes in seawater [Li+]: Evidence from fluid inclusions.

Secular variations in the major ion chemistry and isotopic composition of seawater on multimillion-year time scales are well documented, but the causes of these changes are debated. Fluid inclusions in marine halite indicate that the Li concentration in seawater [Li+]SW declined sevenfold over the past 150 million years (Ma) from ~184 μmol/kg H2O at 150 Ma ago to 27 μmol/kg H2O today. Modeling of the lithium geochemical cycle shows that the decrease in [Li+]SW was controlled chiefly by long-term decreases in ocean crust production rates and mid-ocean ridge and ridge flank hydrothermal fluxes without requiring changes in continental weathering fluxes. The decrease in [Li+]SW parallels the 150 Ma increase in seawater Mg2+/Ca2+ and 87Sr/86Sr, and the change from calcite to aragonite seas, KCl to MgSO4 evaporites, and greenhouse to icehouse climates, all of which point to the importance of plate tectonic activity in regulating the composition of Earth's hydrosphere and atmosphere.

Plate tectonic control of strontium concentration in Phanerozoic and Neoproterozoic seawater: Evidence from fluid inclusions in marine halite

Chemical analyses of 1371 fluid inclusions in 131 halite samples with marine 87Sr/86Sr values were used to reconstruct the strontium concentrations [Sr]SW of Phanerozoic and Neoproterozoic seawater. [Sr]SW varied seven-fold and oscillated twice between high- and low-Sr concentrations over the past 550 million years (Myr), in rhythm with Ca-rich and SO4-poor paleoseawater intervals and calcite-aragonite seas. Variations in the [Sr]/[Ca]SW ratio from fluid inclusions were not significant over the past ∼270 Myr, and are within ±3 µmol/mmol of the modern [Sr]/[Ca]SW ratio of ∼8.5 µmol/mmol. These results agree with the [Sr]/[Ca]SW ratios obtained from fossil corals, benthic foraminifera, brachiopods, belemnites, and rudists. [Sr]/[Ca]SW in the early and middle Paleozoic was ∼2 times the modern [Sr]/[Ca]SW ratio. A major shift of the [Sr]/[Ca]SW ratio in the late Permian coincided with the initial rifting of the Pangean supercontinent. Seawater 87Sr/86Sr ratios plotted against 1/[Sr]SW show two distinct linear correlations: negative correlation from 515 to 252 Ma and positive correlation from 150 to 0 Ma, suggesting different controls on the global Sr cycle between these intervals. The negative correlation coincides with the long-term assembly of Pangea in the Paleozoic (∼500–250 Ma). The positive correlation from 150 to 0 Ma parallels the break-up of Pangea and the decrease of mid-ocean ridge (MOR) hydrothermal fluid flux and subduction zone length in the Mesozoic and Cenozoic.

Reconstruction of Dead Sea lake level and mass balance back to 237 ka BP using halite fluid inclusions

The lake level of the Dead Sea, Southern Levant, has fluctuated with an amplitude of ∼250 m in response to the last glacial-interglacial cycle. This exceptional sensitivity to climate change, and the availability of long sedimentary archives, make the Dead Sea a benchmark for long quantitative paleohydrological reconstructions. However, discontinuities and chronological uncertainties in the marginal sedimentary record have hampered the reconstruction of Dead Sea lake levels beyond the Last Glacial (70–14 ka before present, BP). Here, we apply a two-pronged methodology. First, we measure the lake water density along ICDP deep core 5017-1-A using a new method, Brillouin spectroscopy on two-phase halite fluid inclusions; we combine it with the composition of pore water and the thickness of halite layers in the core to reconstruct lake level, volume, mass balance and subsidence rate. Second, we tune the chronology of lake levels from outcrops by matching it to the chronology of the deep core. The resulting lake level reconstruction, spanning 237–70 ka BP, is validated by the excellent agreement between outcrop- and mass balance-based methodologies. It shows a long-term recession of the lake, its level decreasing from one interglacial to the other, down to a Holocene record low. There are two reasons for this lake level fall. First, with an average rate of 2.65 ± 0.15 m/ka, subsidence has outpaced sedimentation at least over the last ∼130 ka. Second, by reducing the solute inventory of the lake, massive halite precipitation events such as that of 131–116 ka BP have durably increased surface water activity and evaporation, and thus lowered the lake level, up to today. Conversely, our analysis suggests that, during 191–11 ka BP, the dissolution of Mount Sedom salt diapir and freshwater inflows provided to the lake about three times the mass of solute NaCl contained in the modern Dead Sea (in 1985). This massive solute influx, occurring mainly during glacial highstands, strongly contributed to lowering surface water activity and evaporation and, therefore, to increasing the lake volume. Our results suggest that Dead Sea lake levels are more accurately interpreted in terms of climatic change if surface water activity is taken into account.

Термометричні дослідження флюїдних включень у баденському галіті Карпатського регіону в контексті встановлення глибини солеродного басейну

It was established that in order to avoid errors in the interpretation of paleotectonic conditions of salt formation based on fluid inclusions in halite, the primary stage of the research should be the genetic identification of the sedimentation textures of halite and fluid inclusions in this mineral. For the thermometric study of inclusions and to determine the depth of the sedimentation basin based on the obtained data, only thermal test chambers are suitable which provide the possibility of observing groups of inclusions in different zones of sedimentary halite, as, for example, in the micro thermal test chamber designed by Prof. V. A. Kalyuzhny. In the course of the research, the equipment of the thermometric method, which is based on the use of a microthermal test chamber designed by V. A. Kalyuzhny, was modernized. In particular, the material of the thermal chamber (stainless steel) was replaced with copper, which made it possible to avoid excessive thermal gradients into chamber and to increase the permissible heating rate by 20 times due to the higher thermal conductivity of copper. For the same purpose, the glass optical windows of the camera were replaced with leukosapphire windows, which have a much higher thermal conductivity. The measuring system of the installation is made on a miniature platinum resistance thermometer with an electronic measuring unit. These improvements made it possible to achieve high system stability and good reproducibility of measurement results. Using the thermometric method, it was established that the temperature of sedimentation at the bottom of the Badenian salt basin of the Carpathian region was 19.5–20.5; 20.0–22.0; 24.0–26.0 °C, and on the surface of the brine was 34.0–36.0 °C. On this basis, a model of the basin with a pronounced thermocline and a total thickness of the water column of up to 30 meters was built, which is the most likely to establish the features of sedimentation. Crystallization of halite at different depths in basins with a thermocline can explain the presence of so-called “low-temperature” (24.0–25.0 °C) and “high-temperature” (37.8–42.6 °C) bottom halite in a number of ancient salt-bearing basins.

Ca2+] and [SO[formula omitted]] in Phanerozoic and terminal Proterozoic seawater from fluid inclusions in halite: The significance of Ca-SO4 crossover points

Chemical analyses of 2,618 (1,640 new and 978 published) fluid inclusions in marine halite were used to define paleoseawater [Ca2+] and [SO2−4] over the past 550 million years (Myr). Three types of fluid inclusion brine chemistries were recognized based on measured [Ca2+] and [SO2−4]: (1) SO4-rich with [SO2−4] ≫ [Ca2+]; (2) Ca-rich with [Ca2+] ≫ [SO2−4]; and (3) Ca-SO4 crossover points with [Ca2+] ≈ [SO2−4]. The SO4-rich and Ca-rich fluid inclusion chemistries oscillated twice in the terminal Proterozoic and Phanerozoic. Transitions between SO4-rich and Ca-rich seas, here called “Ca2+−SO42−crossover points” occurred four times: terminal Proterozoic–Early Cambrian (544–515 Ma), Late Pennsylvanian (309–305 Ma), Triassic–Jurassic boundary (∼200 Ma), and Eocene–Oligocene (36–34 Ma). New fluid inclusion analyses using laser ablation-inductively coupled plasma-mass spectrometry better defined the [Ca2+] and [SO2−4] in seawater at the Late Pennsylvanian and Eocene–Oligocene crossover points and the timing of the Triassic–Jurassic crossover point. Crossover points coincide with shifts in seawater Mg2+/Ca2+ ratios, the mineralogies of marine non-skeletal carbonates and shell building organisms (aragonite vs. calcite) and potash evaporites (MgSO4 vs. KCl types). Phanerozoic and terminal Proterozoic trends in seawater [Ca2+] and [SO2−4] also coincide with supercontinent breakup, dispersal, and assembly cycles, greenhouse–icehouse climates, and modeled atmospheric pCO2. Paleoseawater [Ca2+] and [SO2−4] were calculated from the fluid inclusion data using the assumption that the [Ca2+] × [SO2−4] ranged from 150 to 450 mmolal2, which is 0.5–1.5 times the [Ca2+] = 11 × [SO2−4] = 29 product in modern seawater (319 mmolal2). Two additional end-member scenarios, independent of the [Ca2+] × [SO2−4] = 150–450 mmolal2 assumption, were tested using constraints from fluid inclusion [Ca] and [SO4]: (1) constant [SO2−4] = 29 mmolal as in modern seawater, and variable [Ca2+], and (2) constant [Ca2+] = 11 mmolal as in modern seawater and variable [SO2−4]. Mg2+/Ca2+ ratios calculated from the three scenarios were compared to independent data on the Mg2+/Ca2+ ratios from skeletal carbonates (echinoderms and corals) and mid-ocean ridge flank calcite veins. Constant [Ca2+] of 11 mmolal is unlikely because this relatively low concentration generated unreasonably low seawater [SO2−4] during most of the past 550 Myr and high Mg2+/Ca2+ ratios compared to independent data. Constant [SO2−4] of 29 mmolal produced unreasonably high seawater [Ca2+] and lower Mg2+/Ca2+ ratios than those derived from fluid inclusions, echinoderms, corals, and calcite veins. Variable [Ca2+] and [SO2−4] showed the best agreement with the Mg2+/Ca2+ ratios derived from fluid inclusions, echinoderms, corals, and calcite veins.

830-million-year-old microorganisms in primary fluid inclusions in halite

Abstract Primary fluid inclusions in bedded halite from the 830-m.y.-old Browne Formation of central Australia contain organic solids and liquids, as documented with transmitted light and ultraviolet–visible (UV-vis) petrography. These objects are consistent in size, shape, and fluorescent response with cells of prokaryotes and eukaryotes and with organic compounds. This discovery shows that microorganisms from saline depositional environments can remain well preserved in halite for hundreds of millions of years and can be detected in situ with optical methods alone. This study has implications for the search for life in both terrestrial and extraterrestrial chemical sedimentary rocks.

Estimation of the Ambient Temperatures during the Crystallization of Halite in the Oligocene Salt Deposit in the Shulu Sag, Bohaiwan Basin, China

The centimeter-scale halite rhythmites in the first member of the Shahejie Formation in the Shulu Sag of the Bohai Bay Basin are investigated, and the Eocene to early Oligocene paleoenvironmental characteristics of a typical saline lake basin are restored by reconstructing the temperature and compositional information of ancient brines. The obtained homogenization temperatures (Th) of fluid inclusions range from 6.5 to 49.2 °C, with a relative lower Th from transparent halite samples than from gray halite samples. This suggests different temperature conditions and a probable association with seasonal changes. The ion contents of halite fluid inclusions reveal the lake brine is a Na-Mg-K-Ca-Cl type and reached the initial stage of halite deposition. The transparent halite samples plotted within different phase regions than the gray halite samples on plots of ion contents and showed significant change within phase regions. Combined with the observed cm-scale rhythm in the evaporite sequences of the Shulu Sag, these results suggest a shallow water environment and frequent dilution by inflows of fresher water caused by seasonal climate change. The gray halite formed under higher temperatures and increased inflow conditions, and the transparent halite formed under lower temperatures and decreased inflow conditions. Compared with the Jiangling Sag in Hubei Province in southern China, the Shulu Sag may have been less affected by igneous rocks in the Es1 Formation due to the material source, and the concentration of trace elements such as lithium, strontium and boron in the ancient salt lake brine was lower.

Redox conditions in Late Permian seawater based on trace metal ratios in fluid inclusions in halite from the Polish Zechstein Basin

Previous studies have confirmed that primary fluid inclusions in halite record and preserve information concerning the major ion chemistry of seawater. Here, we determine ratios of redox sensitive trace metals (Fe, Mn, V, Mo, U) in paleo-seawater trapped as primary fluid inclusions in halite from two boreholes (Przyborów IG3, Gorzów Wielkopolski IG1) from the Polish sector of the European Southern Permian Basin and estimate the original seawater concentrations of the redox sensitive trace metals.Our results show generally higher ratios of Fe/U, Fe/Mo, and Fe/V in fluid inclusions in halites associated with sulfate-depleted (calcium-rich) brines, compared to inclusions in halites formed in association with sulfate-rich brines in the Przyborów IG3 borehole. This behavior is consistent with the interpretation of García-Veigas et al. (2011) to reflect changes in redox conditions from oxidizing (represented by sulfate-rich brines) to reducing (represented by sulfate-depleted and calcium-rich brines) in the Zechstein epicontinental sea during the Late Permian. The correlation is more complex in halites from the Gorzów Wielkopolski IG1 borehole, likely reflecting local controls on redox state.Results suggest that ratios of Mn/U, Mn/V, and Mn/Mo in fluid inclusions may be used to refine redox conditions in the water column when these data are evaluated in combination with Fe/U, Fe/Mo, Fe/V, and Mn/Fe ratios because reduction of Mn(III, IV) to Mn(II) occurs at a higher redox potential compared to that required to reduce Fe(III) to Fe(II).The estimated original Mn and Mo concentrations in the seawater in the Late Permian Zechstein Basin are generally within the concentration range observed in modern anoxic basins while concentrations of V and Fe are generally higher and U is generally lower. Our results suggest that trace metal abundances in fluid inclusions in halite vary in response to redox changes in seawater and provide a potential redox proxy. To better understand and apply results obtained from fluid inclusions in halite as a paleoredox proxy, however, further work is required. These include the study of fluid inclusions in halite from more locations worldwide and the more detailed characterization of redox sensitive trace metal behavior during seawater evaporation.

Reconstruction of Polyhalite Ore-Formed Temperature from Late Middle Pleistocene Brine Temperature Research in Kunteyi Playa, Western China

Kunteyi Salt Lake (KSL), located in the northwest of the Qaidam Basin (QB), is rich in polyhalite resources. However, there is no relevant research on the ore-formed temperature of polyhalite in nature, such as KSL. The homogenization temperature ( T h ) of salt mineral inclusions can directly reveal the form temperature of minerals. In view of the poor diagenesis of polyhalite in KSL, almost no polyhalite crystals are formed. Therefore, the ore-formed temperature of polyhalite in KSL is revealed by using the T h of fluid inclusions in halite associated with polyhalite as a substitute index. A total of 472 T h data from 34 halite samples and 34 maximum homogenization temperature ( T hMAX ) data ranged from 17.1°C to 35.5°C, among which 24 data were concentrated at 17-23°C and the average value is 22.1°C. Brine temperature of other salt lakes in QB and paleoclimate characteristics of the study area were combined. It suggests that the temperature conditions of polyhalite mineralization in the study area are generally low. However, under the overall low-temperature background, polyhalite seems to be easily enriched at relatively high temperature; for example, the content of polyhalite is generally high in the first relatively dry and hot salt-forming period, and the brine temperature at the peak stage of polyhalite at 45 m is relatively high, which indicates that the high temperature conditions promote the formation of polyhalite in KSL. As far as the overall relationship between temperature and polyhalite is concerned, polyhalite is deposited at both low temperature and relatively high temperature, which verifies the previous understanding that polyhalite is a mineral with wide temperature phase, and also shows that temperature has a limited effect on polyhalite formation under natural conditions. In addition, combined with the chemical composition of halite fluid inclusions, it is found that the concentration of Mg2+ in nature has an influence on the temperature measurement process. According to the previous experimental research, speculate that the actual temperature of ancient brine and ore-formed temperature of polyhalite in KSL are lower than the measured T h . The confirmation of the influence of Mg2+ on temperature measurement is convenient for more accurate reconstruction of the metallogenic temperature of evaporite such as polyhalite. The research on the ore-formed temperature of KSL polyhalite enriches and perfects the polyhalite mineralization theory and provides theoretical basis for the basic and applied research of polyhalite.

Ore-Forming Fluid Evolution of Shallow Polyhalite Deposits in the Kunteyi Playa in the North Qaidam Basin

Polyhalite occurrence in the Kunteyi Playa in the Qaidam Basin has been known for many years. However, the genetic mechanism of this deposit remains unclear. In this study, a typical section in the playa depocenter is selected to study the polyhalite mineralogy combined with the homogenization temperature and composition of halite fluid inclusions in shallow evaporitic strata. The results show that 1) the main evaporite minerals in the strata are halite and polyhalite; no common gypsum is found; 2) analyses of homogenization temperatures of halite fluid inclusions indicate that a higher temperature is needed for polyhalite generation compared with other saline minerals; and 3) the fluid inclusion chemical analysis shows that they are sulfate-type minerals with a shortage of Ca. Thus, it can be concluded that the formation of polyhalite is not related to gypsum replacement, and deep oilfield brines may provide a Ca source and a higher temperature for polyhalite formation, where the mixing and interaction occurred between K- and Mg-enriched sulfate brines and deep Ca-enriched brines under the control of climate and tectonics in the study area. While most polyhalite was generated natively, some formed during secondary generation, which was potentially related to replacement with carnallites or sylvites.

The Temperature of Halite Crystallization in the Badenian Saline Basins, in the Context of Paleoclimate Reconstruction of the Carpathian Area

Currently, fluid inclusions in halite have been frequently studied for the purpose of paleoclimate reconstruction. For example, to determine the air temperature in the Middle Miocene (Badenian), we examine single-phase primary fluid inclusions of the bottom halites (chevron and full-faceted) and near-surface (cumulate) halites collected from the salt-bearing deposits of the Carpathian region. Our analyses showed that the temperatures of near-bottom brines varied in ranges from 19.5 to 22.0 °C and 24.0 to 26.0 °C, while the temperatures of the surface brines ranged from 34.0 to 36.0 °C. Based on these data, such as an earlier study of lithology and sedimentary structures of the Badenian rock salts, the crystallization of bottom halite developed in the basin from concentrated and cooled near-surface brines of about 30 m depth. Our results comply with the data on the temperature distribution in the modern Dead Sea.

Halogenases of Qarhan Salt Lake in the Qaidam Basin: Evidence From Halite Fluid Inclusions

The fluid inclusion composition of halite can help track chemical composition of ancient fluids and, thus, serves as a reliable index to analyze ancient brine in salt lakes. Qarhan Salt Lake (QSL) is the largest potash brine deposit in China. Although the mixing of modern river water and Ca-Cl deep water is widely accepted as potassium formation, the mixing characteristics in the time domain and driving factors of deep water are still unclear. Here, the chemical composition of fluid inclusions in primary halite samples collected from the ISL1A borehole in QSL was measured by LA-ICP-MS technology. The analysis results show that, during the formation stage of the S4 salt layer in QSL, the main potassium salt layer, the contents of Ca2+ and Sr2+ in brine increased significantly. There is evidence confirming that Ca-Cl deep water is beneficial to the enrichment of potassium and the surrounding rivers generally develop terraces. It suggests that, during the formation stage of the QSL potassium salt layer, more Ca-Cl inflow water of the northern margin supplies the salt lake, inferring that it was driven by tectonic activities. In addition, the chemical composition of halite fluid inclusions shows that there is an anomaly in geochemistry at the early stage of salt formation in QSL. By combining the time of tectonic activities, it is inferred that the anomaly is not caused by tectonic activities but maybe caused by a salt-forming event. This work indicates that deep water and tectonic movement have a huge impact on the evolution of salt lakes. Therefore, it is necessary to consider the influence of deep water and tectonic activities on the salt-forming evolution stage of salt lakes when studying the salt-forming evolution stage of salt lakes and paleoclimate by using salt lake deposition.

Ancient Microorganisms and Carotenoids Preserved in Fluid Inclusions in Halite from Chaka Salt Lake, Western China: Evidence from Micro‐observation and in situ Raman Spectroscopy

AbstractTrapped ancient microorganisms in halite fluid inclusions are of special interest to the understanding of biology and ecology in salt lake systems. With the integration of petrologic, microthermometric, and Raman spectroscopic analyses, this study utilizes fluid inclusions from Chaka Salt Lake, eastern Qaidam Basin, NW China, to assess the possibility of microorganism‐trapping by fluid inclusions. Here, we report that the solid phase of some primary fluid inclusions contains carotenoids, which is interpreted as evidence of Dunaliella algae, and that the coexisting liquid phase comprises SO42‐. The homogenization temperatures of single‐phase primary fluid inclusions indicate that the precipitation temperature of the Holocene halite in Chaka Salt Lake ranges from 13.5°C to 36.4°C. This suggests that fluid inclusions in halite are a good medium for trapping and preserving ancient microorganisms and organic matter in salt lakes, and that Raman spectroscopy has good potential to identify halophilic archaea.

Mid-Eocene sea surface cooling in the easternmost proto-Paratethys sea: constraints from quantitative temperatures in halite fluid inclusions

The temperature fluctuations in the Eocene climate are one of the most mysterious phenomena in Cenozoic climate dynamics, and they severely affected the marine and terrestrial biospheres. However, quantitative and comprehensive temperature reconstructions for middle Eocene climatic variations remain limited due to fragmentary paleotemperature records, especially in the easternmost proto-Paratethys sea (Kuqa Depression), where traditional paleoclimatic proxies are restricted by the occurrence of extensive and thick evaporite deposits. In this study, we reconstruct middle Eocene sea surface temperatures (SST) and even air temperatures in the Kuqa Depression based on 584 homogenization temperatures (Th) for fluid inclusions in cumulate and chevron halite crystals from cores DW1 and KL4. The Th values from core DW1 have ranges of 10.5–45.7 °C, the Th values from core KL4 have ranges of 12.6–35.2 °C. The measured Th values are mainly concentrated within 20–30 °C, and an average Th value of 25.6 °Crepresents the SST and is consistent with previous coeval research results. The highest recorded Th is 45.7 °C, clearly representing local hot climate conditions. The average and maximum SST in the middle Eocene Kuqa Depression are cooled by 5.2–11.3 °C and 6.5–14.1 °C, respectively. The cooling trend in the Kuqa Depression occurred in response to global and Tethyan realm cooling in the middle Eocene, but the cooling amplitude in the study area was greater than that of the global climate. The Th data for primary halite fluid inclusions can effectively and quantitatively track past environmental and climatic variations, especially in evaporitic basins where traditional paleoclimatic proxies are often not available.

The brine depth of the Khorat Basin in Thailand as indicated by high-resolution Br profile

Bromine contents of a 17-cm halite core from drilling hole of K203 in the Khorat Basin were analysed at 1 cm intervals (17 samples in total). The Br contents range from 99 to 184 ppm with a rapid variation. The K/Mg ratios of halite samples are tens of times higher than those of primary halite fluid inclusions. There is no positive correlation between Mg and Br contents, suggesting that fluid inclusions impose very little or negligible influence on Br contents of halites. The Br contents are not controlled by potash minerals either because the SEM examination shows no potash minerals and there is no relationship between K and Br contents. The Br contents of halite are thus primarily controlled by the Br concentrations of parent brines. The rapid variation of Br contents of halite within this section suggests a shallow saline pan wherein the giant Khorat evaporites were formed. This is contradictory to previous Br profiles of the Lower Salt Member which showed relatively stable and continuously increasing trends. The shallow saline pan model evidenced by high-resolution Br profile is consistent with sedimentary facies and salt mineral textures.

Whether the Middle Eocene Salt-Forming Brine in the Kuqa Basin Reached the Potash-Forming Stage: Quantitative Evidence from Halite Fluid Inclusions

The Kuqa Basin is an important potentially potash-bearing basin in China, and thick salt-bearing strata were deposited under the influence of multistage Tethyan transgression-regression cycles during the Eocene. At present, research on the process of potash formation in the Kuqa Basin has mostly focused on traditional salt mineralogy, whole-rock geochemistry, and evaporite sedimentary evolution characteristics. However, research on the original ore-forming parent fluid directly related to potash formation has not yet been carried out, directly hindering further evaluation of potash mineralization. Therefore, this paper takes the internal factors controlling potash formation as the starting point and analyzes the physical and chemical properties, such as the homogenization temperatures ( T h ) and chemical compositions, of primary halite fluid inclusions. A total of 220 T h data from fluid inclusions were obtained, and the temperatures ranged from 9.4 to 54.1°C, indicating a high-temperature brine environment conducive to the rapid deposition of the potash deposit. In total, 22 halite fluid inclusions were analyzed for chemical components. The highest KCl content reached 0.59%, which was higher than the lowest industrial grade of potassium-rich brine (0.5%), indicating that the brine experienced a high degree of evaporation and concentration during the salt-forming period and reached the potash precipitation stage. This paper provides quantitative data on the evolution of the sedimentary environment in the Kuqa Basin and supports future potash exploration.