Search Results (8)

Research of the depositional environment using geological mapping, petrography, gamma-ray (GR) log, palynology, and foraminifera fossils of the Bojongmanik Formation has led to the formation of several different conclusions about the transition to the marine environment, which are attractive to revisit. The expected results of this research are to determine the paleoenvironment of the Bojongmanik and Serpong Formations based on elemental geochemistry, the development of paleoenvironment proxies based on portable X-ray fluorescence (pXRF) in fluvial to transitional environments studies, and the contribution of paleoenvironment analysis to GR-log facies interpretation. The research methodology starts with GR-log facies analysis, Pearson’s correlation, paleoenvironment analysis based on elemental affinity and elemental ratio, and comparing the paleoenvironment with GR-log-based facies. The paleoenvironment analysis based on elemental geochemistry resulted in the Bojongmanik Formation in the research area deposited at the tidal point bar, lagoon, and shoreface, while the Serpong Formation was deposited at the fluvial point bar and floodplain. Compared to previous research, the Bojongmanik Formation in the research area could be stratigraphically related to the upper Bojongmanik Formation. Proxies based on elemental geochemical affinities of carbonate-associated, carbonate-productivity, terrigenous-associated elements, and redox-sensitive trace elements show contrast changes between facies. Proxies based on the specific ratio show a detailed paleoenvironment for paleoclimate (Sr/Cu), paleosalinity (Sr/Ba), paleoredox (Cu/Zn), paleo-hydrodynamics and water depth (Zr/Rb and Fe/Mn), sediment provenance (Cr/Zr), and siliciclastic-dominated (Zr + Rb)/Sr. Adding a geochemistry element-based paleoenvironment analysis benefits from a more specific justification for GR-log facies interpretation. Full article

X-ray fluorescence (XRF) core scanners are commonly used for fine-scale geochemical analysis in sediment studies, but data are semi-quantitative and require calibration to convert geochemical element counts to concentrations. Application of XRF core scanning in soil science remains largely untapped. This study employed an ITRAX core scanner to scan grassland soil cores and developed a novel calibration method based on a chemometric approach to characterise soil geochemistry. As soil samples are collected based on depth sampling, this study investigated whether higher resolution element concentrations could be inferred from lower resolution reference samples and if regression models from multiple cores could apply to a new core at the same resolution. Reference concentrations were obtained for all cores at 10 cm intervals, with validation conducted at 1 cm for a single core. Two calibration curve types were proposed: one based on the single core’s 10 cm data to validate references at 1 cm intervals; and another using all cores, with each core serving as a test item after exclusion from the training set. Various preprocessing measures and feature selection techniques were tested. Results showed successful calibration for elements Ca, P, Zn, Sr, and S, with high $R^2$ values of 0.94, 0.93, 0.93, 0.92 and 0.91, respectively. The study presents a novel method for calibrating XRF core scanning element counts, demonstrating its potential for high-resolution soil analysis. Full article

The Upper Silesian Coal Basin (USCB), located in southern Poland, is the major coal basin in Poland, and all technological types of hard coal, including coking coal, are exploited. It is also an area of high potential for coal-bed methane (CBM). Despite the increasing availability of alternative energy sources globally, it is a fact that the use of fossil fuels will remain necessary for the next few decades. Therefore, research on coal-bearing formations using modern research methods is still very important. The application of geochemistry and chemostratigraphy in reservoir characterization has become increasingly common in recent years. This paper presents the possibility of applying chemostratigraphic techniques to the study of the Carboniferous coal-bearing succession of the Upper Silesian Coal Basin. The material studied comes from 121 core samples (depth 481–1298 m), representing the Mudstone Series (Westphalian A, B). Major oxide concentrations of Al₂O₃, SiO₂, Fe₂O₃, P₂O₅, K₂O, MgO, CaO, Na₂O, K₂O, MnO, TiO₂, and Cr₂O₃ were obtained using X-ray fluorescence (XRF) spectrometry. Trace elements were analyzed using inductively coupled plasma mass spectrometry (ICP/MS). The geochemical record from the Mudstone Series shows changes in the concentration of major elements and selected trace elements, leading to the identification of four chemostratigraphic units. These units differ primarily in the content of Fe, Ca, Mg, Mn, and P as well as the concentration of Zr, Hf, Nb, Ta, and Ti. The study also discusses quartz origin (based on SiO₂ and TiO₂), sediment provenance and source-area rock compositions (based on Al₂O₃/ TiO₂, TiO₂/Zr, and La/Th), and paleoredox conditions (based on V/Cr, Ni/Co, U/Th, (Cu+Mo)/Zn, and Sr/Ba) for the chemostratigraphic units. Chemostratigraphy was used for the first time in the study of the Carboniferous coal-bearing series of the USCB, concluding that it can be used as an effective stratigraphic tool and provide new information on the possibility of correlating barren sequences of the coal-bearing succession. Full article

Portable X-ray fluorescence (pXRF) is a useful geochemical technique employed to explore toolstone procurement strategies in the lithic record, commonly utilized in sourcing obsidians. Non-obsidian volcanic toolstones (e.g., dacites, rhyolites, basalts, and andesites) are abundant in interior Alaskan assemblages yet understudied compared to obsidian. Geochemical analyses of these non-obsidian materials offer the potential to gain new insights into ancient toolstone provisioning behaviors. This paper presents a synthesis of geochemical (pXRF) analyses of rhyolite artifacts, systematic regional raw material surveys, and lithic technological analyses collected from nineteen late Pleistocene and Holocene assemblages from the Nenana valley, interior Alaska. Previous research studies on archaeological rhyolites from the region are replicated, new rhyolite artifact groups are identified, and one new rhyolite source is reported and described here. Ultimately, this paper contributes to a growing body of geochemical research seeking to provide a more nuanced look at the complex late Pleistocene and Holocene record of eastern Beringia. Full article

Several techniques, such as chemical methods and inductively coupled plasma mass spectrometry (ICP-MS), are available to accurately determine element content. However, they are time-consuming, labor-intensive, or expensive. Portable X-ray fluorescence spectrometry (pXRF) can be applied in various scenarios, with significantly higher efficiency and cost-effectiveness than laboratory methods. However, it also has limitations such as lower detection capability, relatively high detection limits, and lower accuracy than laboratory methods. In this study, we focused on applying pXRF to determine the elemental content of sediment samples and investigate its use in mineral exploration. A variety of factors influencing the results of pXRF analysis were analyzed. Our results showed that pXRF could detect more than 30 elements in stream sediments. The reliability of pXRF’s measurements was affected by factors such as the kind of element, sediment particle size, sample grinding treatment, count time, averaged element content, standard deviation of content, and range of content variation. The combination of pXRF analysis and laboratory analysis of partial samples is adequate for establishing a multi-element content inference equation. With this equation, it is possible to effectively infer the content gradient of elements, which will provide valuable support for mineral resource exploration. Full article

The Yamaat Uul mafic complex with Cu-Ni mineralization is located in the Khangai Mountains of Western Mongolia. We have received new unique data for mafic rocks of the complex: U-Pb dating (SHRIMP II), mineralogy (WDS) and geochemistry (XRF, ICP-MS), Sm-Nd and Rb-Sr isotope data and sulphur isotopes. The Yamaat Uul mafic complex consists of two intrusions: Intrusion 1 is represented by rocks of plagioclase cumulates and olivine–pyroxene cumulates; Intrusion 2 consists of monzogabbro. Intrusions 1 and 2 are different in composition of minerals such as olivine, plagioclase and biotite. The monzogabbro has higher contents of incompatible elements (REE, K, Ti, P) than rocks of Intrusion 1. Zircon U-Pb dating of the anorthosite and Bt-Am-Ol gabbronorite shows a Late Permian age (255.8 ± 2.9 Ma and 262.6 ± 3.1 Ma, respectively) for the Yamaat Uul mafic complex. All of the rocks of the complex are derived from a unified parental melt due to different amounts of trapped melts in plagioclase and olivine–pyroxene cumulates and without crustal contamination. The Cu-Ni mineralization of the complex has a low degree of evolution of the sulphide melt, similar to PGE-Cu-Ni mafic–ultramafic intrusions of the Khangai Mountains (Nomgon and Oortsog Uul). The Yamaat Uul mafic complex together with other mafic–ultramafic intrusions of the Khangai Mountains is related to the Khangai LIP and can be considered as potential for the PGE-Cu-Ni. The new geological, petrological, geochemical and isotope–geochronological data can later be used to reconstruct the geotectonics of the Khangai Mountains and the Central Asian orogenic belt as a whole. Full article

The Pingshuo Mine is an important coal mine of the Ningwu coalfield in northern Shanxi Province, China. To investigate the mineralogy and geochemistry of Pingshuo coals, core samples from the mineable No. 4 coals were collected. The minerals, major element oxides, and trace elements were analyzed by scanning electron microscopy (SEM), LTA-XRD in combination with Siroquant software, X-ray fluorescence (XRF), inductively coupled plasma mass spectrometry (ICP-MS) and ICP-CCT-MS (As and Se). The minerals in the Pennsylvanian coals from the Pingshuo Mine dominantly consist of kaolinite and boehmite, with minor amounts of siderite, anatase, goyazite, calcite, apatite and florencite. Major-element oxides including SiO₂ (9.54 wt %), Al₂O₃ (9.68 wt %), and TiO₂ (0.63 wt %), as well as trace elements including Hg (449.63 ng/g), Zr (285.95 μg/g), Cu (36.72 μg/g), Ga (18.47 μg/g), Se (5.99 μg/g), Cd (0.43 μg/g), Hf (7.14 μg/g), and Pb (40.63 μg/g) are enriched in the coal. Lithium and Hg present strong positive correlations with ash yield and SiO₂, indicating an inorganic affinity. Elements Sr, Ba, Be, As and Ga have strong positive correlations with CaO and P₂O₅, indicating that most of these elements may be either associated with phosphates and carbonates or have an inorganic–organic affinity. Some of the Zr and Hf may occur in anatase due to their strong positive correlations with TiO₂. Full article

This paper reports the mineralogy and geochemistry of the Early Permian No. 5 coal from the Chuancaogedan Mine, Junger Coalfield, China, using optical microscopy, scanning electron microscopy (SEM), Low-temperature ashing X-ray diffraction (LTA-XRD) in combination with Siroquant software, X-ray fluorescence (XRF), and inductively coupled plasma mass spectrometry (ICP-MS). The minerals in the No. 5 coal from the Chuancaogedan Mine dominantly consist of kaolinite, with minor amounts of quartz, pyrite, magnetite, gypsum, calcite, jarosite and mixed-layer illite/smectite (I/S). The most abundant species within high-temperature plasma-derived coals were SiO₂ (averaging 16.90%), Al₂O₃ (13.87%), TiO₂ (0.55%) and P₂O₅ (0.05%). Notable minor and trace elements of the coal include Zr (245.89 mg/kg), Li (78.54 mg/kg), Hg (65.42 mg/kg), Pb (38.95 mg/kg), U (7.85 mg/kg) and Se (6.69 mg/kg). The coal has an ultra-low sulfur content (0.40%). Lithium, Ga, Se, Zr and Hf present strongly positive correlation with ash yield, Si and Al, suggesting they are associated with aluminosilicate minerals in the No. 5 coal. Arsenic is only weakly associated with mineral matter and Ge in the No. 5 coals might be of organic and/or sulfide affinity. Full article