Fluid Carbon Research Articles

Evaluation of movable fluid and controlling factors in lacustrine gravity-flow tight sandstone reservoirs: Implications for predicting reservoir quality

Lacustrine gravity-flow tight sandstone reservoirs are rich in petroleum resources, and the presence of movable fluids is essential for the efficient recovery of tight oil. However, characterizing the properties of movable fluids and predicting their content are challenging due to the limited data available on these fluids. To address this research gap, it is imperative to conduct a comprehensive study on the distribution patterns and controlling factors of movable fluids within the lacustrine gravity-flow tight sandstone reservoirs of the Chang-7 Member in the Heshui region of the Ordos Basin. The study utilized a range of analytical techniques, such as thin section analysis, scanning electron microscopy (SEM), high-pressure mercury injection (HPMI), constant-rate mercury injection (CRMI), and nuclear magnetic resonance (NMR). We identified three distinct lithofacies and three types of pore-throat spaces within these lacustrine gravity-flow sandstones. The highest amount of movable fluid was observed in the submicron pore throats, followed by nanopore throats, while the micron pore throats exhibited the lowest amount. Our analysis indicates that petrophysical parameters, mineral composition, and pore throat structures collectively influence the content of movable fluids. Specifically, quartz and feldspar content are positively correlated with the movable fluid content, while clay and carbonate cement content are negatively correlated. Fine sandstones with massive bedding typically have a high content of movable fluids, which is associated with elevated quartz and feldspar content. In contrast, very fine sandstones to siltstones with parallel or ripple beddings have a very low content of movable fluids, characterized by high levels of carbonate and clay cementation. The study also suggests that the lower limit of the pore throat radius of movable fluid is about 0.03 μm. These findings offer novel insights for evaluating and predicting high-quality lacustrine gravity-flow tight sandstone reservoirs, enabling more effective exploration and development strategies.

High-Quality Foaming and Weight Reduction in Microcellular-Injection-Molded Polycarbonate Using Supercritical Fluid Carbon Dioxide under Gas Counter Pressure.

Microcellular injection molding (MuCell®) using supercritical fluid (SCF) as a foaming agent to achieve weight reduction has become popular in carbon emission reduction. In the typical MuCell® process, SCF N2 is commonly used. Although SCF CO2 exhibits high solubility and can achieve a high weight reduction, controlling the foaming is not easy, and its foaming cells are usually larger and less uniform, which limits its industrial application. Our previous studies have shown that gas counter pressure (GCP) can improve the foaming quality effectively. Here, we investigated whether or not the CO2 SCF foaming quality could be improved, and weight reduction was achieved for polycarbonate (PC) material. This is quite important for the electronics industry, in which most of the housing for devices is made of PC materials. MuCell® was subjected to molding experiments using the parameters of the SCF dosage, melt temperature, mold temperature, and injection speed. The results revealed that using CO2 gas for the PC material can reduce the size of microcellular cells to 40 µm and increase the cell densities to 3.97 × 106 cells/cm3. Using GCP significantly improved the microcellular injection-molded parts by reducing the cell size to 20.9 µm (a 45.41% improvement) and increasing the cell density to 8.04 × 106 cells/cm3 (a 102.48% improvement). However, implementing GCP may slightly decrease the target weight reduction. This study reveals that microcellular injection molding of PC parts using SCF CO2 can achieve high-quality foaming and reduce the weight by about 30%.

Raman Spectroscopic Data of the Quenching Phases of a Pt Solution in a Low Water Reduced Carbonic Fluid at P = 200 and T = 950–1000°C

Raman Spectroscopic Data of the Quenching Phases of a Pt Solution in a Low Water Reduced Carbonic Fluid at P = 200 and T = 950–1000°C

Metasedimentary “carbon filter” and its implication for subduction zone carbon recycling

The movement of carbon in subduction zones plays a crucial role in regulating the global carbon cycle, controlling Earth's climate, and maintaining its habitability. Recent work suggests that only a fraction of the carbon released from subducting slabs at sub-arc depths is ultimately released from volcanic arcs, necessitating the existence of hidden carbon reservoirs within the slab-to-arc pathways. However, the precise location of these reservoirs remains enigmatic. Slab fluid serves as the primary medium for carbon transport in subduction zones; thus, a comprehensive understanding of fluid-rock interaction during slab fluid migration is essential for reconciling the carbon flux imbalance between the slab and the arc. In this study, we explore rock carbonation along a fluid conduit in the Southwestern Tianshan HP metamorphic belt in northwest China. Field evidence and petrologic observation reveal significant carbonation of a siliciclastic metasediment at its contact with a high-pressure garnet-bearing calcite (formerly aragonite) vein. We find that rock carbonation (by progressive Fe-bearing magnesite, dolomite, then aragonite precipitation) occurred when slab-derived carbonic fluids migrated through the metasedimentary sequence at approximately 80 km depth. Furthermore, modeling demonstrates that the metasedimentary layer atop the slab has the capacity to sequester 20%–50% of the fluid carbon from the ascending slab devolatilization flux. We propose that the metasedimentary veneer at the plate interface functions as a “carbon filter”, hindering the transfer of carbon from the slab to the arc and helping to reconcile the carbon flux imbalance between the amount released by the slab and that emitted by the arc. This study also provides insights into decarbonation efficiency and mechanisms, carbon-transfer pathways, and temporal aspects of the subduction zone carbon cycle.

Petrology, phase equilibria modelling, and fluid inclusion study of mafic granulites from Bhavani Suture Zone, Southern India

We report new petrology, mineral chemistry, P–T conditions, and fluid inclusion data on mafic granulites from the Mettupalayam region along the Bhavani Suture Zone, Southern Granulite Terrane, India. Phase equilibria modelling of mafic granulites yielded peak P–T conditions of 780–860 °C and 7.6–10.1 kbar followed by a near isothermal decompression along a clockwise P–T path. The trapped fluid inclusions in the peak metamorphic minerals display a melting temperature range from −57.4 °C to −56.6 °C, close to the triple-point temperature of pure CO2. The primary inclusions homogenized at −18.9 °C to +0.2 °C, corresponding to density values of 0.93–1.03 g/cm3. Homogenization of the secondary inclusions occurred within the range from −6.3 to +18.1 °C, corresponding to low CO2 densities of 0.79–0.96 g/cm3. From the textural characteristics of the high-density primary carbonic fluid inclusions, we interpret these inclusions as the CO2-rich syn-metamorphic fluid present during the high-grade metamorphism. The secondary fluids characterised by lower densities have undergone re-equilibration during the exhumation stage (decompression) from the peak granulite-facies metamorphism along a clockwise P–T trajectory. This interpretation is consistent with the occurrence of hornblende + plagioclase symplectite around the porphyroblastic garnet, suggesting decompression. We infer that the high-density CO2 was the dominant syn-metamorphic fluid components present during the granulite-facies metamorphism in the Mettupalayam region. Such carbonic fluids, possibly derived by degassing from carbonates or mantle sources, probably played a significant role in stabilizing high-grade mineral assemblages along this collisional suture zone.

Peritectic reaction of olivine in the diamond-forming system carbonate-silicate-(C-O-H) at 6 GPa

Influence of the supercritical C-O-H-fluid (7.5 wt.%) onto melting phase relations of the multicomponent multiphase diamond-forming system olivine-jadeite-diopside-(Mg-Fe-Ca-Na-carbonates)-(C-O-H) in experiments at 6 GPa and 700–1200 °C (the upper mantle conditions) has been studied. The peritectic reaction of olivine and jadeite-bearing melt with garnet formation has been retained as a key mechanism of the ultrabasic-basic evolution of diamond-forming melts. The CO2-fluid and silicate components react forming carbonate phases. The H2O-fluid together with carbonates has essentially lowered temperatures of the liquidus and solidus boundaries. The phase of supercritical water fluid and water-bearing carbonate nesquehonite (Nes) MgCO3·3H2O were identified with the Raman-spectroscopy method after crystallization of the completely mixed silicate-carbonate-(C-O-H-fluid) melt.

Post–peak petrochronology and C–O–H fluid influx in the lower crust: A case study of garnet–orthopyroxene granulites from the Rauer Islands, East Antarctica

Garnet–orthopyroxene granulites from the Rauer Islands (East Antarctica) provide a spectacular example to investigate the late fluid evolution, metamorphic duration, and behavior of monazite and zircon in response to metamorphic reactions and fluid–rock interaction. Here, we characterize the secondary fluid inclusions in peritectic garnet and orthopyroxene, which occur as multiphase inclusions along micro–fractures. Inclusions are composed of siderite, pyrophyllite, calcite, quartz and residual CO2, representing stepdaughter phases resulting from the interactions between C–O–H fluid and its hosts at variable temperatures during retrogression. Zircon grains show clear core–rim structure, which yield 206Pb/238U ages of 540–507 Ma and 527–490 Ma, respectively. Index inclusions and internal structures suggest that the cores document the timing of peak and post–peak decompression while the growth of rims corresponds to melt crystallization during the final cooling. The UPb systems in zircons are considered to have not been obviously affected by fluid or melt–mediated modification. The unusual formation of monazites in garnet–orthopyroxene granulites may be linked with the elevated phosphorus budget as a result of apatite dissolution during the prograde melting of the rocks. Detailed investigations suggest that the crystallization of monazites occurred both at peak and post–decompression stages, whose isotopic systematics has been completely reset due to melt–mediated dissolution–precipitation. The spurious dates for monazites (522–495 Ma) are highly coinstantaneous with the dating results for zircon rims, further supporting this view. Therefore, we conclude that the late carbonic fluid influx cannot result in marked U(Th)–Pb resetting in zircon and monazite. Instead, anatectic melt may have played an important role in the disturbance of isotopic systematics in monazites, especially for long–lived high–grade metamorphic terranes. Combined with previously published data, we propose that the Pan–African metamorphic event in the Rauer Islands may have reached the peak at around ∼540 Ma, followed by a protracted post–peak evolution that lasted for at least ∼50 Myr. This study highlights the importance of an integrated investigation of fluid and index mineral inclusions, as well as the chemical signatures of zircon and monazite, to interpret chronological data correctly.

Effects of coil frequency on the carbon transport in the top-seeded solution growth of SiC single crystal

The flow pattern and carbon transport in the solution for the solution growth of silicon carbide (SiC) in an induction-heating system can be effectively controlled by adjusting the coil frequency to obtain a relatively uniform distribution of growth rate. In this paper, a global heat and mass transfer model was first verified by the SiC crystal growth experiment results at the coil frequency of 8 kHz. Then, the influence of coil frequency on the fluid flow, carbon concentration, and growth rate for the growth of SiC crystals was numerically investigated. The results indicated that electromagnetic convection (at low frequencies) greatly enhances the upward convection beneath the crystal and weakens the adverse effects of Marangoni convection, resulting in a uniform distribution of radial temperature along the growth interface. Consequently, the carbon transport from the crucible wall to the crystal center is strengthened, leading to a uniform region of high carbon supersaturation with a lower coil frequency. The optimal radial uniformity of the growth rate along the growth interface is achieved at the coil frequency of 3 kHz.

Ocean acidification in the tropical Indian Ocean over the past 37 years: Insights from [formula omitted]11B and B/Ca records in a Maldives coral

Boron isotopes (δ11B) in coral skeletons of Porites have been widely applied to reconstruct past seawater pH (pHSW) on decadal to centennial timescales. However, due to biological regulation within corals, an additional transfer function is required to estimate ambient seawater chemistry during the skeleton growth under the calcification site fluid pH. Temperature may also interfere with coral calcification fluid pH (pHCF) due to changes in kinetics of coral aragonite precipitation, or buffering capacity in coral calcification fluid. To decipher how coral Porites adjusts pHCF in response to pHSW from complex environmental controls, long-term records from sites with least fluctuations in environmental conditions other than pHSW are essential. Here we present a 37-year record of coral δ11B and B/Ca ratios derived from a coral core collected from southern Maldives, the tropical Indian Ocean. Our results show no clear seasonality in the coral δ11B and B/Ca ratios between monsoons, but a long-term decline in coral pHCF is evident across the entire record. When applying different existing transfer functions, we also observe discrepancies among the calculated pHCF values, model results and short-term instrumental data. Calculated calcification fluid dissolved inorganic carbon concentration ([DIC]CF) values are relatively low compared to literature, suggesting that coral calcification fluid carbonate chemistry may be under different levels of control, even within the same coral taxa. Thus, coral records from a wider geographic range are required to better quantify coral response to ocean acidification, and our results can serve as a baseline for future comparisons.

Ferric Iron in Eclogitic Garnet and Clinopyroxene from the V. Grib Kimberlite Pipe (NW Russia): Evidence of a Highly Oxidized Subducted Slab

Abstract Estimates of oxygen fugacity of eclogitic rocks are linked to the redox evolution of the oceanic protolith during subduction and its residence in the lithospheric mantle, and, based on knowledge of pressures and temperatures, allow modelling of the speciation of volatile elements and diamond (or graphite) versus carbonate stability. To date, the oxygen fugacity of mantle eclogites has been shown to vary between −6 (Kasai, Congo and Udachnaya, Siberia) and −0.1 (Udachnaya, Siberia) log units (relative to the fayalite–magnetite–quartz buffer, FMQ), linked to the low Fe3+ contents of garnets. In this study, we investigated the Fe oxidation state of coexisting garnet and clinopyroxene hand-picked out of 17 diamond-free high-MgO and low-MgO mantle eclogites (dated at 2.84 Ga) from the Grib kimberlite pipe (East-European platform). Measured Fe3+/∑Fe values range between 0.03 and 0.19 for garnet and 0.18–0.38 for clinopyroxene, the former being higher than what was measured previously in garnets equilibrated at mantle conditions. The Fe3+/∑Fe of the reconstructed bulk rock ranges between 0.10 and 0.15 for high-MgO eclogites and 0.10 and 0.24 for low-MgO eclogites (with uncertainties of ± 0.02 and ± 0.03 in both cases). Thermobarometric calculations result in equilibration pressures and temperatures of 3.0–5.2 (± 0.4) GPa and 720–1050 (± 60) °C for both high-MgO and low-MgO eclogites, slightly lower than previous P–T estimates of mantle eclogites from the Udachnaya kimberlite pipe (Siberian craton). At these conditions, ∆logfo2 (FMQ) calculated using the available oxythermobarometric model varies from −1.7 to −0.6 log units for high-MgO eclogites and from −2.9 to 0.9 log units for low-MgO eclogites. Samples recording ∆logfo2 (FMQ) ≤ −1 log units overlap with North Slave, West Africa and Udachnaya eclogites, with no difference among eclogite types. The average values of −1.2 (± 0.4) log units for high-MgO and −0.6 (± 1.1) log units for low-MgO eclogites suggest different redox conditions of basaltic protoliths during subduction worldwide. Previous geochemical studies on the same rock samples reported evidence of cryptic metasomatism in both garnet and clinopyroxene that we demonstrate being not recorded by their major elements, while modal metasomatism evidenced by the presence of phlogopite as a product of interaction with a kimberlitic melt only affects the MgO of the bulk rock. Therefore, we suggest that high Fe3+/∑Fe ratios for garnet (> 0.10) and for reconstructed bulk rocks in the case of both low-MgO and high-MgO samples cannot be due to metasomatic interaction with an oxidized fluid, but rather are the consequence of Fe3+ redistribution in an unusually oxidized mafic protolith upon metamorphism. Our results highlight the redox variability of eclogites of Archaean age at conditions more oxidized than present-day mid-ocean ridge basalts (MORBs) and imply an oxidizing nature of the convective mantle source where magma was formed with consequent speciation of C in the form of carbonate fluid explaining, therefore, the lack of eclogitic diamonds in V. Grib kimberlite pipe.

Characteristics of rock fissure fillings and their relationship with the accumulation of uranium and associated elements in the Kailu Sag of the southern Songliao Basin, Northeast China

The relationship between deep fluids and the enrichment of uranium and associated elements in sedimentary basins remains unclear. Sandstone-type uranium deposits in the southern Songliao Basin exhibit abundant fault systems, and evidence of hot fluid activity is present in the ore-bearing strata, including the presence of hydrothermal minerals such as galena and sphalerite. To elucidate this relationship, we conducted detailed thin-section observations and micro-X-ray fluorescence spectroscopic analysis on the fissure fillings of mafic rocks, granite, sandstone, and mudstone in or near the ore-bearing strata. Our findings indicate that rock fissures are filled with minerals such as pyrite, quartz, ankerite, and calcite, suggesting that deep fluids have multiple sources and stages. Specifically, ankerite, rich in Fe and Mn, is closely associated with uranium mineralization, and is observed in both the fissure fillings and the ore-bearing strata. Fluids enriched in elements such as Tb and Dy likely originate from or are related to the mantle, while fluids with few other components may come from deep strata. However, U and Re contents are low in the fissure fillings, being insufficient for their mineralization. Furthermore, given the high content of carbonate minerals in the ore-bearing strata and their close association with uranium mineralization, we analyzed fluid inclusions and carbon–oxygen isotope composition of the carbonate minerals present in the rock fissures. Fluid inclusions in carbonate minerals indicate moderate to low temperatures (ranging from 145.5 to 298.5 ℃, with an average of 215.3 ℃) and low salinities (ranging from 0.18 to 7.99 wt%, with an average of 2.22 wt%). δ13CV-PDB values of carbonate minerals ranges from − 15.1 ‰ to 0.4 ‰, and δ18OV-SMOW values range from 0.5 ‰ to 14.4 ‰, suggesting a composite genesis of carbonate fluids involving magma and atmospheric precipitation. These test results on fissure fillings match roughly with those of the ore-bearing strata, indicating that deep fluids have infiltrated into the ore-bearing strata and contributed to uranium mineralization. Therefore, we propose that the U and Re enrichment in the ore-bearing strata originates from supergene fluids, whereas deep fluids may provide ore-forming materials such as ankerite, reducing fluids, and heat sources for uranium mineralization.

Fluid–Melt–Rock Interaction during the Transition from Magmatism to HT-UHT-Granulite- and Amphibolite-Facies Metamorphism in the Ediacaran Adrar–Suttuf Metamafic Complex, NW Margin of the West African Craton (Southern Morocco)

Abstract Underplated mafic intrusions ponded at the base of the lower continental crust in extensional settings can experience ultra-high-temperature (UHT) granulite-facies metamorphism during tens of My due to slow cooling rates. These intrusions are also the source of heat and carbonic fluids for regional high-temperature (HT) granulite-facies metamorphism in the continental crust. This work analyses the fluid–melt–rock interaction processes that occurred during the magmatic to HT-UHT-granulite- and amphibolite-facies metamorphic evolution of high-grade mafic rocks from the Eastern Ediacaran Adrar–Suttuf Metamafic Complex (EASMC) of the Oulad Dlim Massif (West African Craton Margin, Southern Morocco). P–T conditions were determined using Ti-in-amphibole thermometry, two-pyroxene and amphibole–plagioclase thermobarometry, and phase diagram calculations. The thermobarometric study reveals the presence of tectonically juxtaposed lower- and mid-crustal blocks in EASMC that experienced decompression-cooling paths from, respectively, UHT and HT granulite-facies conditions at ca. 1.2 ± 0.28 GPa and 975 ± 50°C, and ca. 0.82 ± 0.15 GPa and 894 ± 50°C, to amphibole-facies conditions at ca. 0.28 ± 0.28 GPa and 787 ± 45°C (precision reported for the calibrations at 1 s level). An age for the magmatic to UHT granulite-facies metamorphic transition of 604 Ma was constrained from published SHRIMP Th–U–Pb zircon ages of the igneous protoliths. An amphibole 40Ar–39Ar cooling age of 499 ± 8 Ma (precision at 2 s level) was obtained for the lower-crustal blocks. Amphibole 40Ar–39Ar closure temperatures of 520–555°C were obtained for an age range of 604–499 Ma and an average constant cooling rate of 4.2°C/My, suggesting that the lower-crustal blocks cooled down to the greenschist–amphibolite facies transition in ca. 100 My. During the high-temperature stage, interstitial hydrous melts assisted textural maturation of the rock matrix and caused incongruent dissolution melting of olivine and pyroxenes, and, probably, development of An-rich spikes at the grain rims of plagioclase, and local segregation of pargasite into veins. Subsequent infiltration of reactive hydrous metamorphic fluids along mineral grain boundaries during cooling down to amphibolite-facies conditions promoted mineral replacements by coupled dissolution-precipitation mechanisms and metasomatism. Ubiquitous dolomite grains, with, in some cases, evidence for significant textural maturation, appear in the granoblastic aggregates of the high-grade mafic rocks. However, calculated phase relationships reveal that dolomite could not coexist with H2O–CO2 fluids at HT-UHT granulite- and low-medium P amphibolite-facies conditions. Therefore, it is proposed that it may have been generated from another CO2-bearing phase, such as an immiscible carbonatitic melt exsolved from the parental mafic magma, and preserved during cooling due to the prevalence of fluid-absent conditions in the granoblastic matrix containing dolomite. The lower-crustal mafic intrusions from EASMC can represent an example of a source of heat for granulitisation of the mid crust, but a sink for carbon due to the apparent stability of dolomite under fluid-absent conditions.

The Potential Antinociceptive Effect and Mechanism of Cannabis sativa L. Extract on Paclitaxel-Induced Neuropathic Pain in Rats Uncovered by Multi-Omics Analysis.

Cannabis sativa L. (hemp) is a herbaceous plant rich in cannabinoids with a long history of use in pain treatment. The most well-characterized cannabinoids, cannabidiol (CBD) and Δ9-tetrahydrocannabinol (Δ9-THC), garnered much attention in chemotherapy-induced peripheral neuropathy (CIPN) treatment. However, few studies have investigated the biological benefits and mechanism of hemp extract on CIPN. In the present study, hemp extract (JG) rich in cannabinoids was extracted by supercritical fluid carbon dioxide extraction (SFCE). The antinociceptive efficacy was evaluated using a paclitaxel-induced peripheral neuropathy (PIPN) rat model based on behavioral tests. Further omics-based approaches were applied to explore the potential mechanisms. The results showed that JG decreased mechanical allodynia, thermal hyperalgesia, and inflammatory cytokines in PIPN rats significantly. Transcriptome analysis identified seven key genes significantly regulated by JG in PIPN model rats, mainly related to the neuroactive ligand-receptor interaction pathway, PPAR signaling pathway, and cAMP signaling pathway. In metabolomic analysis, a total of 39 significantly altered metabolites were identified, mainly correlated with pentose and glucuronate interconversions and the glycerophospholipid metabolism pathway. Gut microbiota analysis suggested that increased community Lachnoclostridium and Lachnospiraceae_UCG-006 in PIPN rats can be reversed significantly by JG. In conclusion, hemp extract exhibited antinociceptive effects on PIPN. The analgesic mechanism was probably related to the regulation of inflammation, neuroactive ligand-receptor interaction pathway, sphingolipid metabolism, etc. This study provides novel insights into the functional interactions of Cannabis sativa L. extract on PIPN.

Characteristics of MWCNT, SWCNT, Cu and water based on magnetized flow of nanofluid with Soret and Dufour effects induced by moving wedge: Consequence of Falkner–Skan power law

Soret and Dufour effects are utilized in designing efficient heat exchangers, optimizing separation processes, and understanding biological transport phenomena. A wedge-shaped structures aid in aerodynamics, optics, seismic resistance, and biological studies. Due to these application the consequences Soret and Dufour effects on flow of nanofluid due to wedge have been investigated. The characteristics of water ( H 2 O ) as a base fluid and single-walled carbon nanotubes ( SWCNTs ) , multi-walled carbon nanotubes ( MWCNTs ) , and copper ( Cu ) nanoparticles are taking into account. The influence of thermal radiation and heat source/sink are part of this investigation. Similarity variables are used to sort out the complexity of fundamental governing equations. Maple via Runge–Kutta–Fehlberg method (RKF45) is used to solve resulting system of ordinary differential equations (ODEs). The graphical and tabulated results of velocity, temperature, and concentration profiles are plotted against different parameters involved in this study. The findings indicate that modifying the moving wedge factor reduces the temperature distribution. By increasing value of magnetic constraint the velocity distribution increased, the temperature and concentration distribution both are increased for varying the value of Dufour, and Soret and source/sink parameters.

Comparison of antimicrobial activities of oregano, lavender, sage, anise and clove extracts obtained by supercritical fluid carbon dioxide extraction and essential oils obtained by hydrodistillation

ABSTRACT The aim of the study was to compare the extraction yields, chemical compositions and antimicrobial activities of essential oils obtained by hydrodistillation (HD) and volatile extracts obtained by supercritical fluid extraction extraction (SFE) from oregano (Origanum onites), lavender (Lavandula angustifolia), sage (Salvia officinalis), anise (Pimpinella anisum) and clove (Syzygium aromaticum). Essential oil compounds (EOCs) of the obtained materials from both techniques (HD and SFE) were determined by GC-MS/FID. Agar well diffusion method was used for the determination of antimicrobial activities on five different foodborne microorganisms (Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli Enterococcus faecalis and Klebsiella pneumoniae). According to the results; extraction yields of SFE were found to be higher than HD for all tested aromatic plants. Active ingredient ratios (carvacrol, camphor, anethole, eugenole and linalol) varied depending on the extraction methods. SFE extracts were higher antimicrobial activity than HD essential oils, except clove extract on E. faecalis.

Exploring the pore fluid origin and methane-derived authigenic carbonate properties in response to changes in the methane flux at the southern Ulleung Basin, South Korea

We investigated the geochemistry of gas, pore fluid, and methane-derived authigenic carbonate (MDAC) from four sites in the southern Ulleung Basin, South Korea. In contrast to Sites 16GH-P1 and 16GH-P5, Sites 16GH-P3, and 16GH-P4 are characterized by acoustic chimney structures associated with gas flux. The composition of gas and isotopic signatures of methane (CH4) (C1/C2+ > 300, δ13CCH4 < -60‰, δDCH4 ≤ -190‰) indicate microbial source CH4 at all sites. The upward migration of CH4 can affect the chemical and isotopic properties of pore fluid and gas-related byproducts (e.g., gas hydrate (GH) and MDAC) within the shallow sediments including the current sulfate-methane transition (SMT) (< 5 meters below seafloor). Although no GH was found, elevated Cl- concentrations (maximum = 609 mM) with low δD and δ18O values in Site 16GH-P4 pore fluids delineate the influence of massive GH formation in deeper sediment. In contrast, relatively constant Cl-, δD, and δ18O values in fluids from Sites 16GH-P1, 16GH-P3, and 16GH-P5 indicate a predominant origin from seawater. Pore fluids also exhibit higher concentrations of H4SiO4, B, Mg2+, and K+, along with increasing alkalinity compared to seawater. These observations suggest that marine silicate weathering alters fluid chemistry within the sediment, affecting element and carbon cycles. High alkalinity (up to 60 mM) and Mg2+/Ca2+ ratios (> 6) alongside decreasing Ca2+ and Sr2+ concentrations imply carbonate precipitation. MDACs with diverse morphologies, mainly composed of aragonite and magnesian calcite, and characterized by low carbon isotopic values (δ13CMDAC < -31.3‰), were found at Sites 16GH-P3 and 16GH-P4. Interestingly, δ13CMDAC values at Site 16GH-P3 are clearly differentiated above and below the current SMT. High δ13CMDAC values above the SMT (> -34.3‰) suggest the combined influence of seawater and CH4 migrating upward on MDAC precipitation, whereas low δ13CMDAC values below it (< -41.6‰) indicate a predominant impact of CH4 on MDAC formation. Additionally, the vertical variation of δ18OMDAC values at Site 16GH-P4, compared to the theoretical values, reflects an association with GH dissociation and formation. Our findings improve the understanding of fluid, gas, and MDAC geochemistry in continental margin cold seeps, providing insights into global carbon and element cycles.

Origin of Zn-Pb Mineralization of the Vein Bt23C, Bytíz Deposit, Příbram Uranium and Base-Metal Ore District, Czech Republic: Constraints from Occurrence of Immiscible Aqueous–Carbonic Fluids

The mineralogical, fluid inclusion, and stable isotope (C, O) study was conducted on a Late Variscan Zn-Pb vein Bt23C, Příbram uranium and base-metal district, Bohemian Massif, Czech Republic. The vein is hosted by folded Proterozoic clastic sediments in exo-contact of a Devonian-to-Lower-Carboniferous granitic pluton. Siderite, dolomite-ankerite, calcite, quartz, baryte, galena, sphalerite, V-rich mica (roscoelite to an unnamed V-analogue of illite), and chlorite (chamosite) form the studied vein samples. The banded texture of the vein was modified by the episodic dissolution of earlier carbonates and/or sphalerite. Petrographic, microthermometric, and Raman studies of fluid inclusions proved a complicated fluid evolution, related to the activity of aqueous fluids and to an episode involving an aqueous–carbonic fluid mixture. Homogenization temperatures of aqueous inclusions decreased from ~210 to ~50 °C during the evolution of the vein, and salinity varied significantly from pure water up to 27 wt.% NaCl eq. The aqueous–carbonic fluid inclusions hosted by late quartz show highly variable phase compositions caused by the entrapment of accidental mixtures of a carbonic and an aqueous phase. Carbonic fluid is dominated by CO2 with minor CH4 and N2, and the associated aqueous solution has a medium salinity (6–14 wt.% NaCl eq.). The low calculated fluid δ18O values (−4.7 to +3.6‰ V-SMOW) suggest a predominance of surface waters during the crystallization of dolomite-ankerite and calcite, combined with a well-mixed source of carbon with δ13C values ranging between −8.2 and −10.5‰ V-PDB. The participation of three fluid endmembers is probable: (i) early high-temperature high-salinity Na>Ca-Cl fluids from an unspecified “deep” source; (ii) late low-salinity low-temperature waters, likely infiltrating from overlying Permian freshwater partly evaporated piedmont basins; (iii) late high-salinity chloridic solutions with both high and low Ca/Na ratios, which can represent externally derived marine brines, and/or local shield brines. The source of volatiles can be (i) in deep crust, (ii) from interactions of fluids with sedimentary wall rocks and/or (iii) in overlying Permian piedmont basins containing, in places, coal seams. The event dealing with heterogeneous CO2-bearing fluids yielded constraints on pressure conditions of ore formation (100–270 bar) as well as on the clarification of some additional genetic aspects of the Příbram’s ores, including the reasons for the widespread dissolution of older vein fill, the possible re-cycling of some ore-forming components, pH changes, and occasionally observed carbon isotope shift due to CO2 degassing.

Multiple growth of zirconolite in marble (Mogok metamorphic belt, Myanmar): evidence for episodes of fluid metasomatism and Zr–Ti–U mineralization in metacarbonate systems

Abstract. Fluid infiltration into (meta-)carbonate rocks is an important petrologic process that induces metamorphic decarbonation and potential mineralization of metals or nonmetals. The determination of the infiltration time and the compositional features of reactive fluids is essential to understand the mechanism and process of fluid–rock interactions. Zirconolite (ideal formula: CaZrTi2O7) is an important U-bearing accessory mineral that can develop in metasomatized metacarbonate rocks. In this study, we investigate the occurrence, texture, composition, and chronology of various types of zirconolite from fluid-infiltrated reaction zones in dolomite marbles from the Mogok metamorphic belt, Myanmar. Three types of zirconolite are recognized: (1) the first type (Zrl-I) coexists with metasomatic silicate and oxide minerals (forsterite, spinel, phlogopite) and has a homogeneous composition with high contents of UO2 (21.37 wt %–22.82 wt %) and ThO2 (0.84 wt %–1.99 wt %). (2) The second type (Zrl-II) has textural characteristics similar to those of Zrl-I. However, Zrl-II shows a core–rim zonation with a slightly higher UO2 content in the rims (average of 23.5 ± 0.4 wt % (n=8)) than the cores (average of 22.1 ± 0.3 wt % (n=8)). (3) The third type (Zrl-III) typically occurs as coronas around baddeleyite and coexists with polycrystalline quartz. Zrl-III has obviously lower contents of UO2 (0.88 wt %–5.3 wt %) than those of Zrl-I and Zrl-II. All types of zirconolite have relatively low rare earth element (REE) contents (< 480 µg g−1 for ΣREE). Microtextures and compositions of the three zirconolite types, in combination with in situ zirconolite U–Pb dating using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), reveal episodic fluid infiltration and element mobilization in the dolomite marbles. The first-stage infiltration occurred at ∼ 35 Ma, leading to the formation of Mg-rich silicates and oxides and accessory minerals (Zrl-I, baddeleyite, and geikielite). The reactive fluid was characterized by high contents of Zr, Ti, U, and Th. After that, some Zrl-I grains underwent a local fluid-assisted dissolution–precipitation process, which produced a core–rim zonation (i.e., the Zrl-II type). The final stage of fluid infiltration, recorded by the growth of Zrl-III after baddeleyite, took place at ∼ 19 Ma. The infiltrating fluid of this stage had relatively lower U contents and higher SiO2 activities than the first-stage infiltrating fluid. This study illustrates that zirconolite is a powerful mineral that can record repeated episodes (ranging from 35 to 19 Ma) of fluid influx, metasomatic reactions, and Zr–Ti–U mineralization in (meta-)carbonates. This mineral not only provides key information about the timing of fluid flow but also documents the chemical variation in reactive fluids. Thus, zirconolite is expected to play a more important role in characterizing the fluid–carbonate interaction, orogenic CO2 release, and the transfer and deposition of rare metals.

Patterns of trace element composition of caustobiolites and carbonic fluids according to the results of correlation analysis: A summary of results

Trace element analysis is a well-known research method. The article discusses the results of calculations of correlation coefficients of trace element composition of samples with model chemical content of the Upper, Middle and the Lower crust and biota. Unlike the commonly used methods for comparing the content of individual elements and groups of elements, this method, based on the use of the entire set of available trace element data, provides more robust results. The factual basis of the analysis is a database compiled of a large number of analyzes by different authors and including trace element composition data of organic matter of rocks, solid caustobiolites and hydrocarbon and carbonic deep fluids. The results of correlation coefficient calculations at a quantitative level confirm the previously made conclusions of the polygenic source of trace elements in naphthides, mud volcanic and carbonic fluids. The method makes it possible to estimate the depth of bottom the corresponding fluid systems and the dominant type of the original organic matter. A number of new relationships between the correlation coefficient values of the trace element compositions of the studied natural substances are revealed, in particular, the trend of changes in the correlation coefficients values of trace element content in specimens with the composition of the Earth’s crust and biota in the process of transformation of the initial organic matter into oil and further into oil degradation products. The results of the analysis testify in favor of the previously proposed model of massive oil genesis according to the scheme of a non-equilibrium flow reactor. Confirmation of this model allows us to propose on its basis a system of predictive indicators of possible high oil and gas content, which is required by practice in connection with the depletion of reserves of shallow traditional hydrocarbon deposits.

Porites' coral calcifying fluid chemistry regulation under normal- and low-pH seawater conditions in Palau Archipelago: Impacts on growth properties

Ongoing ocean acidification is known to be a major threat to tropical coral reefs. To date, only few studies have evaluated the impacts of natural long-term exposure to low-pH seawater on the chemical regulation and growth of reef-building corals. This work investigated the different responses of the massive Porites coral living at normal (pHsw ~ 8.03) and naturally low-pH (pHsw ~ 7.85) seawater conditions at Palau over the last decades. Our results show that both Porites colonies maintained similar carbonate properties (pHcf, [CO32−]cf, DICcf, and Ωcf) within their calcifying fluid since 1972. However, the Porites skeleton of the more acidified conditions revealed a significantly lower density (~ 1.21 ± 0.09 g·cm−3) than the skeleton from the open-ocean site (~ 1.41 ± 0.07 g·cm−3). Overall, both Porites colonies exerted a strong biological control to maintain stable calcifying fluid carbonate chemistry that favored the calcification process, especially under low-pH conditions. However, the decline in skeletal density observed at low pH provides critical insights into Porites vulnerability to future global change.