Guangzhou Institute of Geochemistry
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The influence of chondrules on sub-mm fragment shape distributions in Allende impact experiments
The surfaces of sub -kilometer -sized asteroids directly explored by spacecraft, such as Itokawa, Ryugu and Bennu, are covered with blocks and/or regolith particles, whose shapes are considered clues to understanding their formation and evolution on the asteroid 's surface. Ryugu particles returned by the Hayabusa2 mission are likely fragments resulting from impacts because their shapes resemble impact fragments from laboratory experiments. However, there is a lack of laboratory impact experiments examining the shapes of fragments in carbonaceous chondrites, thought to originate from carbonaceous asteroids such as Ryugu and Bennu. The measured sizes of Ryugu particles are in the mm and sub -mm range, similar to the sizes of chondrules. Also, carbonaceous chondrites are generally structurally weaker than the basalts and granites often used in previous laboratory impact experiments. Differences in the strength of the chondrules and matrix might affect the overall strength of the meteorite. In this study, as a first step towards a better understanding of impact fragment shapes in carbonaceous chondrites, we conducted impact experiments on the carbonaceous meteorite Allende (CV3). A spherical alumina projectile with 1.0 mm and a glass projectile with 0.80 mm in diameter were fired into 1 -2 cm -sized Allende targets at nominal impact velocities of 2.0 and 4.0 km/s, respectively. To investigate the correlation between the chondrules (typically sub -mm in size) and the shapes of fine fragments, we measured the shape distributions of sub -mm impact fragments using X-ray microtomography. We observed several impact fracture surfaces along the chondrule boundaries. In addition, these fragments tended to be rounder than fragments from previous impact experiments. However, because the total number of these fragments is relatively small, the fragments were found to have the same overall shape distribution as previous laboratory impact fragments, Itokawa particles and Ryugu particles. This may imply that impact fragment shapes are independent of the bulk material strength. These findings will be useful for understanding the formation process of regolith layers on asteroid surfaces, Itokawa particles, Ryugu particles, and Bennu particles
Tracing Oils and Gas Accumulation in Complex Petroleum Systems Based on Biomarkers, Light Hydrocarbons, and Diamondoids from Concomitant Crude Oils: A Case Study in the Shawan Sag of the Junggar Basin, NW China
The Shawan Sag is one of the most promising blocks in the western Junggar Basin for natural gas and oil exploration. To date, the research and exploration degree here is still low, and there is limited understanding of the origin and migration of natural gas and oils, which seriously restricts future exploration and development. At least three oil charging episodes and one gas charging episode could be confirmed in the reservoirs on the western slope of the Shawan Sag based on the analysis of concentrations and ratios of hopanes and steranes, diamondoids, and light hydrocarbons. The first and second charging oils originated from the peak and late oil generation window stages of Lower Permian Fengcheng Formation (P(1)f) source rocks, respectively. The third charging oil originated from the late oil generation window stage of source rocks of the Middle Permian lower Wuerhe Formation (P(2)w). Combining the carbon isotopic compositions and the gas composition, the fourth charging gas was derived from the postmature source rocks of Carboniferous(C) and Lower Permian Jiamuhe Formation (P(1)j) and the high-postmature source rock of Lower Permian Fengcheng Formation (P(1)f). The preservation conditions of nature gas in the Mesozoic (T-K) cap rocks in the Shawan Sag, as indicated by methyladamantanes (MAs)/methyldiamantanes (MDs) ratio, are better than those in the Mahu Sag. In this study, the methyladamantane maturity parameters of oils in the reservoirs were proposed to evaluate the maturity and further determine the migration direction of late-charging natural gas. The results suggest that late postmatured natural gases were charged from the southern part to the northwest of the Shawan Sag. Therefore, the southeastern direction of Well SP1 is a favorable area for natural gas exploration in the Shawan Sag. Meanwhile the northern part of the sag is favorable for the exploration of high-mature oil generated from source rocks within the Middle Permian Lower Wuerhe Formation
Aerosol trace element solubility determined using ultrapure water batch leaching: an intercomparison study of four different leaching protocols
Solubility of aerosol trace elements, which determines their bioavailability and reactivity, is operationally defined and strongly depends on the leaching protocol used. Ultrapure water batch leaching is one of the most widely used leaching protocols, while the specific leaching protocols used in different labs can still differ in agitation methods, contact time, and filter pore size. It is yet unclear to which extent the difference in these experimental parameters would affect the aerosol trace element solubility reported. This work examined the effects of agitation methods, filter pore size, and contact time on the solubility of nine aerosol trace elements and found that the difference in agitation methods (shaking vs. sonication), filter pore size (0.22 vs. 0.45 mu m), and contact time (1 vs. 2 h) only led to small and sometimes insignificant difference in the reported solubility. We further compared aerosol trace element solubility determined using four ultrapure water leaching protocols, which are adopted by four different labs and vary in agitation methods, filter pore size, and/or contact time, and observed good agreement in the reported solubility. Therefore, our work suggests that although ultrapure water batch leaching protocols used by different labs vary in specific experimental parameters, the determined aerosol trace element solubility is comparable. We recommend that ultrapure water batch leaching be one of the reference leaching schemes and emphasize that additional consensus in the community on agitation methods, contact time, and filter pore size is needed to formulate a standard operating procedure for ultrapure water batch leaching
Towards interpretable machine learning for observational quantification of soil heavy metal concentrations under environmental constraints
Monitoring heavy metal concentrations in soils is central to assessing agricultural production safety. Satellite observations permit inferring concentrations from spectrum, thereby contributing to the prevention and control of soil heavy metal pollution. However, heavy metals exhibit weak spectral responses, particularly at low and medium concentrations, and are predominantly influenced by other soil components. Machine learning (ML)driven modelling can produce predictions but lacks interpretability. Here, we present an interpretable ML framework for concentration quantification modelling and investigated the contributions of spectral and environmental factors-pH and organic carbon-to the estimation of metals with multiple concentration gradients, as analysed through SHAP (SHapley Additive exPlanations) data derived from four learning-based scenarios. The results indicated that scenarios SHC (spectral, pH, and organic carbon) and SH (spectral and pH) were the most optimal for chromium (Cr) [RPD = 1.42, Adj R2 = 0.62], and cadmium (Cd) [RPD = 1.80, Adj R2 = 0.80]. Under environmental constraints, the spectral predictability for Cr and Cd was improved by 67 % and 87 %, respectively. We concluded that interpretable modelling, utilising both spectral and soil environmental factors, holds significant potential for estimating heavy metals across concentration gradients. It is recommended that samples with higher organic carbon content and lower pH be selected to enhance Cr and Cd predictions. An advanced grasp of interpretable predictions facilitates earlier warning of heavy metal contamination and guides the formulation of robust sampling strategies
Water distribution in pore systems and its influences on gas-bearing property of deep shale: A case study of the Longmaxi Formation in the Luzhou area, southern Sichuan Basin
The deeply-buried (>3500 m) Longmaxi Formation (LMX) shale in the southern Sichuan Basin, China, has become an attractive target for shale gas exploration owing to its huge resource potential. Exploration shows that the deep shale has a wide range of gas-in-place (GIP) contents, with variable gas yields, but the reason remains unclear, especially the impact of pore water on gas-bearing property lacks systematic research. In the present study, a suite of deep LMX shale samples was collected from the well FB1 in the Luzhou area of the southern Sichuan Basin, and techniques such as the pore water content measurements, low-pressure gas (CO2 and N-2) adsorption and high-pressure methane adsorption experiments of the moist and dry samples were employed to investigate the distribution of water in the nanopores and its effects on the gas-bearing property. The results show that the deep shale is characterized by a high water content, with a high water saturation (average up to 69.80%), and the water occurs in both the inorganic and organic pores. The water reduces the effective specific surface area and pore volume of the shale averagely by 79.01% and 22.56%. Consequently, the water results in the decrease of methane adsorption capacity averagely by 45.13%. The GIP content models of two typical shale samples indicate that their total gas content is 3 m(3)/t with decreasing water saturation to <40-50%, especially under overpressure conditions. The gas-bearing property of deep LMX shale reservoirs in the complex faulted zones or structural-complex zones would mainly depend on the pore water content except for the properties of shale itself (e.g., maturity, TOC content, mineral composition, porosity and pore structure)
Nonnegligible contribution of terrigenous sediment inputs from local small watersheds to west regions of the Pearl River Estuary, northern South China Sea shelf
As a crucial "sink" for terrigenous material entering the ocean, provenance of sediments within the coastal zone and continental shelf sea regions holds significant scientific importance in the investigation of global material cycling. Environmental magnetism was proved as an effective and rapid approach for sediment source identification. Detail and systematic magnetic measurements were performed for surface sediment samples collected from the mega Pearl River, local small rivers (Tan, Moyang and Jian rivers) of west Guangdong, coastal zone (CZ) and continental shelf (CS) to analyze the contribution of local small watersheds to marine sediments. The results indicate that detrital river input magnetite and hematite are coexisted in both CZ and CS sediments. Compared to CZ sediments, relatively higher concentration of hematite and finer grain size of magnetite are appeared at CS sediments. By comparing of magnetic parameters, it was inferred that magnetic minerals from the Pearl and Tan rivers are transported and deposited on the coastal zone by Guangdong longshore current. Meanwhile, sediment magnetic parameters in the Moyang and Jian Rivers are similar to the CS sediments, implying the two riverssourced materials were directly transported and deposited at the CS due to their narrow and restricted estuaries, and/or the CS preserves the residual deposits from the two rivers formed during the Last Glacial. Except for the Pearl River, sources of local small rivers significantly contribute to marine sediments at the coastal zone and continental shelf
Gold occurrence and mineralization in the Paleozoic Heijianshan Fe-Cu (-Au) deposit, Eastern Tianshan
Gold (e.g., electrum) has been reported in the Paleozoic Heijianshan Fe-Cu (-Au) or iron oxide-copper-gold-like (IOCG-like) deposit in the Eastern Tianshan, but relationships between gold occurrence and sulfides are unclear. The Heijianshan Fe-Cu (-Au) (or IOCG-like) deposit underwent five alteration and mineralization stages: Pre-ore epidote alteration (Stage I), syn-ore magnetite/iron mineralization (Stage II) followed by pyrite alteration (Stage III) and Cu (-Au) mineralization (Stage IV), and post-ore late veins (Stage V). This deposit mainly has two types of pyrite (A and B) based on pyrite-hematite and pyrite-pyrrhotite-chalcopyrite assemblages. They are euhedral to subhedral and mainly homogenous, with the former having porous or inclusion-rich domains. Trace elements incorporating into pyrite at Heijianshan are mainly controlled by compositions (e.g., As, Co, and Cu), temperature (e.g., Ni and Se), and oxygen fugacity (fO2; e.g., As and Se) of hydrothermal fluids, respectively. The timeresolved depth-concentration profiles suggest trace elements in pyrite and chalcopyrite occur as solid solution (e. g., Co, Ni, Zn, As, and Se) and micro- to nano-sized mineral inclusions (e.g., Cu, Bi, and Pb). The gold occurrence at Heijianshan is invisible as solid solution in Stage III pyrite and Stage IV chalcopyrite and visible as micronsized Stage IV electrum. Moreover, incorporation mechanisms of invisible gold are Au3+ substituting iron or copper in pyrite A and chalcopyrite, respectively, and Au+ incorporating into the vacancy or defect positions of pyrite B. Sulfides texture and geochemical compositions when combined with previous in-situ sulfur isotope suggest that pyrite formation was resulted from interaction between external basinal brines and altered host rocks under different temperature and fO2 conditions. Ongoing fluid-rock reaction led to formation of chalcopyrite +/- electrum veins as Cu (-Au) mineralization at Heijianshan. This study suggests that the prolonged interaction contributes to sulfide formation and Cu (-Au) mineralization in these Paleozoic Fe-Cu or IOCG-like deposits formed in basin-related setting, and the Aqishan-Yamansu belt, Eastern Tianshan has gold mineralization potential
Decontamination promotes the release of incorporated organic contaminants in hair: Novel insights into non-invasive biomonitoring
Human hair is increasingly employed as a non-invasive biomonitoring matrix for exposure to organic contaminants (OCs). Decontamination procedures are generally needed to remove external contamination from hair prior to analysis of OCs. Despite various existing decontamination protocols, their impacts on internally incorporated (endogenous) OCs in hair remain poorly understood. This study aims to quantitatively assess the impact of decontamination procedures on endogenous OCs in hair, and investigate optimal decontamination processes and factors influencing the removal of endogenous OCs. In this study, guinea pig was exposed to 6 OCs (triphenyl phosphate (TPHP), tris(1,3-dichloro-2-propyl) phosphate (TDCPP), and tri-n-butyl phosphate (TNBP), bisphenol A (BPA), perfluorooctanoic acid (PFOA), and phenanthrene (PHE)), and 6 decontamination procedures with different solvents (methanol, n-hexane, acetone, ultrapure water, Triton X-100, and sodium dodecyl sulfate) were used to rinse exposed guinea pig hair. All OCs and three metabolites (diphenyl phosphate (DPHP), dibutyl phosphate (DBP), and bis(1,3-dichloro-2-propyl) phosphate (BDCPP)) were detected in the majority of washing solutions. The decontamination procedures apparently resulted in the release of endogenous OCs from hair. The percentages of residual OCs in hair exhibited a linear or exponential decrease with more washing cycles. Furthermore, the residuals of OCs in hair washed with organic and aqueous solvents showed negative correlations with molecular weight, polarizability, and their initial concentrations. Although these findings need to be validated with a broader range of OCs, the results obtained in this study provide compelling evidence that current hair decontamination procedures have significant impacts on the analysis of endogenous OCs in hair. Therefore, it is important to interpret quantitative data on hair OC concentrations with caution and to thoroughly consider each decontamination procedure during analysis
Source rock and climate model for the Cretaceous Jiufotang Formation, Kazuo Basin, China: Geochemistry and petrography
The Lower Cretaceous Jiufotang Formation, situated in western Liaoning Province, China, has attracted attention for abundant Jehol Biota fossils and the potential to improve understanding of the relationships among climate change, evolution of terrigenous organisms, and organic matter (OM) enrichment in lake systems during the Early Cretaceous. Based on organic petrology and biomarker analyses, this study investigated the depositional environment, OM sources, and enrichment mechanism of Jiufotang mudstone in the Kazuo Basin. Maceral composition shows that the OM source of Jiufotang mudstone shifted from mainly aquatic to terrigenous, and biomarkers such as abundant diterpenoids and retene indicate that terrigenous higher plants were mainly conifers during deposition of the Jiufotang Formation. Pr/Ph ratios (0.07-0.65) show that the studied section was deposited in anoxic bottom water that may be necessary for OM enrichment in lake systems. Gravity flows were accompanied by input of many clastic minerals and oxygenation of bottom waters, which is unfavorable for OM enrichment. Therefore, the best OM enrichment model for lake systems includes anoxic bottom water, stable water column stratification, low sedimentation rates, and high phytoplankton contributions. The climate changed from relatively dry to humid, which drove changes in the OM enrichment model in the lake. More importantly, the climate and terrigenous plant information obtained by biomarkers is useful to reconstruct the ecological environment of the Jehol Biota
Towards Safe Diatomite Sludge Management: Lead Immobilisation via Geopolymerisation
Diatomite, a natural adsorbent rich in active silica, serves as a valuable precursor for geopolymer synthesis. The safe disposal of diatomite as a failed lead (Pb(II)) adsorbent is critical to prevent secondary contamination. This study investigated the immobilisation efficiency of geopolymerisation for Pb(II)-rich diatomite sludge. Low-grade diatomite with high ignition loss was utilised in the synthesis of alkali-activated geopolymers. It was demonstrated that the geopolymers achieved a compressive strength of 28.3 MPa with a 50% replacement rate of metakaolin by diatomite sludge, which was not a compromise in strength compared to that of the geopolymer with no Pb(II) (26.2 MPa). The leaching behaviour of Pb(II) was evaluated using water and acetic acid, yielding concentrations below 3 mg/L and immobilisation efficiencies of 95% in both scenarios. Analytical techniques including Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) elucidated the mineral composition and chemical environment of the geopolymers. These analyses revealed that Pb(II) migrated from diatomite pores, potentially forming soluble hydroxides under sufficient hydroxide, which then participated in condensation with silicon and aluminium monomers, effectively immobilising Pb(II) within amorphous aluminosilicate gels. Furthermore, the formation of the amorphous gels within diatomite pores hindered Pb(II) leaching, encapsulating Pb(II) effectively. This study presents a novel approach to immobilising heavy metals within building materials, enhancing mineral resource utilisation efficiency while addressing environmental contamination concerns