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36 pages, 15890 KB  
Article
Geochemistry and U-Pb-Hf Geochronology of Mesoarchean Granitoids from the Arco Verde Complex: Implications for the Crustal Evolution of the Rio Maria Domain, Carajás Province
by Bruna Karine Correa Nogueira, Jean-Michel Lafon, João Marinho Milhomem Neto, Fábio dos Santos Pereira, Regina Celia dos Santos Silva and Elton Luiz Dantas
Minerals 2026, 16(5), 483; https://doi.org/10.3390/min16050483 (registering DOI) - 2 May 2026
Abstract
The Arco Verde Complex, exposed in the Serra do Inajá region of the Rio Maria Domain (Carajás Province, Amazonian Craton), represents one of the oldest TTG granitoid association of the province (3.00–2.92 Ga). While TTG magmatism is well constrained in the northern domain, [...] Read more.
The Arco Verde Complex, exposed in the Serra do Inajá region of the Rio Maria Domain (Carajás Province, Amazonian Craton), represents one of the oldest TTG granitoid association of the province (3.00–2.92 Ga). While TTG magmatism is well constrained in the northern domain, its southern sector lacks precise geochronological data. This study integrates petrographic, geochemical, U–Pb zircon geochronology, and Nd–Hf isotopes to constrain the age, source, and crustal significance of these granitoids. Uranium–Pb zircon dating of two granodiorites yielded ages of 2979 ± 8 and 2979 ± 11 Ma, extending the 2.98 Ga TTG magmatic episode to the southern sector of the Rio Maria Domain. Geochemical data indicate dominant tonalites formed by partial melting of a similar mafic source at different crustal depths, whereas subordinate granodioritic and monzogranitic rocks show transitional TTG affinities. These features indicate coeval mafic and felsic crust rapidly reworked after formation. Hf and Nd model ages of 3.0–3.2 Ga, with positive εHf–Nd at 2.98 Ga, reinforce the Early Mesoarchean as the main crustal growth period in the province. In addition, we propose that the differentiation of the depleted mantle (DM) beneath the Carajás Province may have initiated around 3.8 Ga. Full article
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12 pages, 2330 KB  
Article
A Helium Ion Linear Accelerator Optimised for Astatine Production
by Maurizio Vretenar, Alessandra Lombardi and Lazar Nikitovic
Instruments 2026, 10(2), 25; https://doi.org/10.3390/instruments10020025 (registering DOI) - 2 May 2026
Abstract
This paper presents the design of a linear accelerator optimised for the production of astatine-211, one of the most effective theragnostics isotopes for targeted alpha therapy of cancer (TAT). When attached to a carrier molecule that selectively binds to cancer cells, this powerful [...] Read more.
This paper presents the design of a linear accelerator optimised for the production of astatine-211, one of the most effective theragnostics isotopes for targeted alpha therapy of cancer (TAT). When attached to a carrier molecule that selectively binds to cancer cells, this powerful alpha emitter enables highly localised cell damage. The 11 m long linac is designed to accelerate an average current of up to 2 mA of fully stripped helium ions to 28.4 MeV, the energy required for 211At production on a bismuth target. The accelerator comprises an alpha particle source, a compact Radio Frequency Quadrupole (RFQ), and a Quasi-Alvarez Drift Tube Linac (QA-DTL). Compared with conventional cyclotron-based solutions, the proposed design provides higher beam current for increased isotope yield, together with reduced beam losses and activation. In addition, compared with a standard Drift Tube Linac (DTL) configuration, the adoption of a QA-DTL structure enables more compact dimensions and improved power efficiency. Full article
21 pages, 4098 KB  
Article
Carbon and Nitrogen Isotopic Signatures as Metabolic Biomarkers of Nodal Metastasis and Recurrence in Oral Squamous Cell Carcinoma
by Katarzyna Bogusiak, Zuzanna Popińska, Marcin Kozakiewicz, Piotr Paneth and Józef Kobos
Cancers 2026, 18(9), 1461; https://doi.org/10.3390/cancers18091461 - 1 May 2026
Abstract
Background/Objectives: Oral squamous cell carcinoma (OSCC) exhibits substantial biological heterogeneity, and current clinicopathological risk stratification incompletely reflects tumor metabolic behavior. Stable isotope ratio mass spectrometry enables the quantitative assessment of carbon and nitrogen isotopic composition, potentially capturing cumulative metabolic reprogramming associated with tumor [...] Read more.
Background/Objectives: Oral squamous cell carcinoma (OSCC) exhibits substantial biological heterogeneity, and current clinicopathological risk stratification incompletely reflects tumor metabolic behavior. Stable isotope ratio mass spectrometry enables the quantitative assessment of carbon and nitrogen isotopic composition, potentially capturing cumulative metabolic reprogramming associated with tumor aggressiveness. This study evaluated whether isotopic signatures of tumor tissue and surgical margins are associated with lymph node metastasis and survival outcomes in OSCC. Methods: In this prospective study, 54 consecutive patients undergoing primary surgical treatment for OSCC were enrolled. Paired samples derived from tumor tissue and surgical margins were analyzed using isotope ratio mass spectrometry to determine the relative abundance of nitrogen-15 and carbon-13 isotopes. The primary endpoint was pathological lymph node metastasis. Secondary endpoints included disease-free survival and overall survival. Paired comparisons were performed using Wilcoxon signed-rank tests with false discovery rate correction. Logistic regression models for nodal metastasis were constructed using Firth penalization with bootstrap internal validation, while survival outcomes were evaluated using Cox proportional hazards models with model complexity restricted according to the number of events. Results: Tumor tissues demonstrated significantly lower δ13C and δ15N values and higher nitrogen-to-carbon ratios compared with surgical margins (all adjusted p < 0.05). In multivariable analysis, tumor δ15N was independently associated with lymph node metastasis and modestly improved model discrimination. However, it was not independently associated with disease-free or overall survival. Exploratory analyses indicated that higher δ13C values in surgical margins were independently associated with shorter disease-free survival. Conclusions: These findings suggest that isotope ratio mass spectrometry-based isotopic profiling identifies reproducible metabolic differences between tumor and margin tissues in OSCC. Tumor δ15N is associated with lymph node metastasis, whereas margin δ13C may reflect recurrence risk and potentially capture metabolic field effects. These findings are hypothesis-generating and warrant validation in larger, independent cohorts. Full article
(This article belongs to the Section Cancer Biomarkers)
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27 pages, 35282 KB  
Article
Relative Cu/Ni Enrichment of the Baixintan Magmatic Ni–Cu Deposit in the Eastern Tianshan Orogen (NW China): Insights from S, Pb, Cu, and Lu–Hf Isotopes
by Mei Zang, Qianru Xiao, Xin Li, Yujun Shi, Ling Xing, Pengbing Li, Peisong Fang, Pingping Zhu, Tedi Fu, Jingnan Ye, Yongming Guo and Zulihar Balatibak
Minerals 2026, 16(5), 481; https://doi.org/10.3390/min16050481 - 1 May 2026
Abstract
Baixintan is a magmatic Ni–Cu sulfide deposit discovered in the central Tuwu–Yandong porphyry Cu belt of the Eastern Tianshan Orogen (ETO) of NW China in 2016. It is in close proximity (~5 km) to the Tuwu Cu deposit, the largest Carboniferous porphyry Cu [...] Read more.
Baixintan is a magmatic Ni–Cu sulfide deposit discovered in the central Tuwu–Yandong porphyry Cu belt of the Eastern Tianshan Orogen (ETO) of NW China in 2016. It is in close proximity (~5 km) to the Tuwu Cu deposit, the largest Carboniferous porphyry Cu deposit (~336 Ma) in Xinjiang. The Baixintan Ni–Cu ore is characterized by a high Cu/Ni ratio, but the reason for it remains unclear. To resolve this question, we present petrographic, geochronological, whole-rock geochemical, and S, Pb, Cu, and Lu–Hf isotopic data. Ore-related hornblende olivine websterite (HOW) and hornblende olivine gabbro (HOG) were emplaced at 296.6 ± 1.1 Ma and 289.7 ± 1.2 Ma, respectively, which were formed in an Early Permian post-collisional extensional setting. Whole-rock Pb and zircon Lu–Hf isotopes suggest that the parental magmas were predominantly mantle-derived. The Baixintan HOW and HOG contain abundant hornblende and are enriched in LILEs and LREEs but depleted in HFSEs, suggesting subduction-related metasomatism in their magma source. The sulfide (chalcopyrite, pyrrhotite, and pentlandite) δ34S values cluster around 0‰ (–0.13 to 0.11, n = 11), and the chalcopyrite has uniformly negative but variable δ65Cu values (–0.96 to –0.13, n = 6), which suggest that the ore-forming materials were mainly derived from the subduction-metasomatized mantle. Olivine Ni contents are significantly lower than those crystallized under sulfide-unsaturated conditions, implying that olivine fractional crystallization was an important trigger for sulfide melt segregation at Baixintan. Baixintan is the only known magmatic Ni–Cu sulfide deposit in the ETO that shares a Cu-preconcentrated, metasomatized mantle source with a giant porphyry Cu system. Copper pre-enrichment in the magma source may be the main factor for the relatively high Cu/Ni ratio observed in the Baixintan deposit. Full article
(This article belongs to the Section Mineral Deposits)
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15 pages, 8832 KB  
Article
Formation Mechanisms and Hydrogeochemical Evolution of a Metasilicate-Strontium Rich Mineral Water in a Subtropical Volcanic Terrain, East China
by Guang Li, Jie Guo, Yewei Song and Fengshan Ma
Water 2026, 18(9), 1086; https://doi.org/10.3390/w18091086 - 1 May 2026
Abstract
Natural mineral waters hosted in volcanic terrains are globally significant, but the co-enrichment mechanisms of metasilicate and strontium remain poorly understood. Here we investigate a Jurassic volcanic-hosted mineral water source in eastern China using hydrochemical analysis, 14C dating, stable isotopes, and structural [...] Read more.
Natural mineral waters hosted in volcanic terrains are globally significant, but the co-enrichment mechanisms of metasilicate and strontium remain poorly understood. Here we investigate a Jurassic volcanic-hosted mineral water source in eastern China using hydrochemical analysis, 14C dating, stable isotopes, and structural analysis. The groundwater is of Ca–Mg–HCO3 type with slightly alkaline pH (7.44–7.63). Metasilicate (26.4–32.9 mg/L) and strontium (0.40–0.83 mg/L) co-enrichment is governed by plagioclase weathering in a bicarbonate-dominated, weakly alkaline environment where SrHCO3+ ion pairs enhance strontium mobility. Pearson-corrected 14C ages of 3900–4900 years reveal that millennial-scale residence time is critical for sufficient water-rock interaction and attainment of regulatory thresholds. A conduit-barrier system formed by NW-trending extensional-shear and NNE-trending compressional-shear faults controls groundwater flow paths and residence times, leading to systematic inter-well hydrochemical differentiation. These findings provide a theoretical basis for the genetic identification, potential evaluation, and sustainable management of high-quality mineral water resources in volcanic terrains. Full article
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23 pages, 4083 KB  
Article
Tracing Groundwater Recharge Sources and Controls on Groundwater Quality in a Delineated Aquifer to Support Groundwater Allocation, De Aar, Northern Cape, South Africa
by Lucky Baloyi, Sikelela Mqhayi, Harrison Pienaar, Mxolisi B. Mukhawana, Mike Butler and Thokozani Kanyerere
Water 2026, 18(9), 1084; https://doi.org/10.3390/w18091084 - 1 May 2026
Abstract
Groundwater-dependent communities such as De Aar require a better understanding of groundwater systems to ensure sustainable allocation. This study aims to trace recharge sources in unconfined and confined aquifers and identify processes controlling groundwater quality using hydrogeochemistry and environmental tracers. It argues that [...] Read more.
Groundwater-dependent communities such as De Aar require a better understanding of groundwater systems to ensure sustainable allocation. This study aims to trace recharge sources in unconfined and confined aquifers and identify processes controlling groundwater quality using hydrogeochemistry and environmental tracers. It argues that aquifer delineation and hydraulic parameters alone cannot fully identify recharge sources or geochemical processes; integrating them with hydrogeochemistry and environmental tracers provides stronger evidence to support groundwater allocation. To validate the argument, the study integrated hydrogeochemical analysis, stable isotopes, tritium, radon-222, and statistical methods supported by depth-specific groundwater sampling. The results, interpreted using Piper and Gibbs diagrams, PHREEQC modelling, and scatter plots, show that groundwater evolution is mainly controlled by rock–water interaction, ion exchange, evaporation, and mixing processes. Ca–HCO3 water indicates recent recharge, while Na–Cl water reflects evaporation effects in both unconfined and confined aquifers, with halite dissolution contributing to Na and Cl enrichment. Isotope results indicate that unconfined aquifer water is isotopically enriched and linked to recent recharge, whereas confined aquifer and spring waters are depleted, suggesting recharge from higher elevations through fractured zones. Tritium dating reveals young (<30 years), intermediate (30–50 years), and old groundwater (60–109 years), while radon results indicate active groundwater flow path, particularly along fractures. These findings demonstrate that groundwater recharge is derived from both local meteoric sources and regional contributions, resulting in predominantly fresh groundwater; however, localized quality concerns should be considered for improved water allocation. Full article
(This article belongs to the Section Hydrogeology)
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19 pages, 20897 KB  
Article
Permian Crustal Reworking and Rare-Metal Mineralization in the Halajun Area, the Southwest Tianshan, NW China
by Haiquan Li, Huanhuan Wu, He Huang, Guoqing Wang, Zhanlin Ge, Ming Liu and Di Hao
Geosciences 2026, 16(5), 181; https://doi.org/10.3390/geosciences16050181 - 1 May 2026
Abstract
Permian A-type granites and associated rare-metal mineralization are widespread in the Halajun area, southwestern Tianshan; however, petrogenetic controls on rare-metal enrichment and mineralization remain under-constrained. Here, we integrate zircon and monazite geochronology, whole-rock geochemistry, and zircon Hf-O isotopes from Halajun I and II [...] Read more.
Permian A-type granites and associated rare-metal mineralization are widespread in the Halajun area, southwestern Tianshan; however, petrogenetic controls on rare-metal enrichment and mineralization remain under-constrained. Here, we integrate zircon and monazite geochronology, whole-rock geochemistry, and zircon Hf-O isotopes from Halajun I and II plutons to constrain the origin of these granites and their metallogenic significance. Zircon U–Pb and monazite ages indicate emplacement at 274–273 Ma, coeval with regional magmatism associated with the Tarim large igneous province. Geochemical signatures—high SiO2, alkali, and rare-earth element (REE) contents, enrichment of HFSE (e.g., Nb, Zr, and Hf), coupled with LILE (e.g., Ba and Sr) depletion—classify these granites as highly differentiated alkaline A-type rocks. Positive εHf(t) values and intermediate δ18O compositions of zircons suggest derivation from partial melting of Neoproterozoic lower crust with input from mantle-derived melts, reflecting significant crust–mantle mixing. Magmatic differentiation, in concert with regional crustal reworking driven by mantle plume activity, produced granites enriched in Nb, Ta, Zr, and REEs, which host the rare-metal mineralization in the region. These results indicate that Permian crustal reworking in the southwestern Tianshan was a driver of high-differentiation magmatism and rare-metal enrichment, highlighting the potential of similar A-type granitic systems in Central Asia for rare-metal exploration. Full article
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17 pages, 6348 KB  
Article
Geochemistry of Metal Sulfides from the Duolong Porphyry Cu-Au Deposit, Tibet: Implications for the Mineralization Process
by Qi Zhang, Huanhuan Yang, She Li, Qin Wang, Yujie Dong, Hongwei Li, Chao Yang, Changyun Gan, Rongkun Zhang, Xuelian Fu and Xinjuan Liang
Minerals 2026, 16(5), 478; https://doi.org/10.3390/min16050478 - 30 Apr 2026
Viewed by 15
Abstract
The Duolong porphyry copper–gold district, located in the northwestern segment of the Bangongco–Nujiang metallogenic belt on the southern margin of the South Qiangtang terrane (Tibet), hosts typical porphyry-style Cu-Au mineralization with well-defined alteration zoning from potassic through chlorite–sericite to propylitic assemblages. Based on [...] Read more.
The Duolong porphyry copper–gold district, located in the northwestern segment of the Bangongco–Nujiang metallogenic belt on the southern margin of the South Qiangtang terrane (Tibet), hosts typical porphyry-style Cu-Au mineralization with well-defined alteration zoning from potassic through chlorite–sericite to propylitic assemblages. Based on integrated in situ major/trace element and sulfur isotope analyses of pyrite and chalcopyrite from different alteration zones, we identify two discrete episodes of magmatic-hydrothermal activity that exerted distinct controls on metal endowment. Sulfur isotope signatures define a systematic evolution from the earliest, high-temperature potassic stage (δ³⁴S: Py-Ⅰ –3.70 to –1.16‰, mean –2.14‰; Cp-Ⅰ –4.92 to –0.90‰, mean –2.54‰) through propylitic alteration (Py-Ⅱ: 1.20–5.16‰, mean 3.06‰) to the later chlorite–sericite stage (Py-Ⅲ: –2.00 to 1.86‰, mean 0.06‰; Cp-Ⅱ: –2.50 to 0.58‰, mean –0.77‰), tracking progressive fluid cooling and changing fluid sources. Trace element systematics further discriminate these episodes: sulfides from potassic and chlorite–sericite zones are enriched in trace elements, whereas propylitic pyrite is depleted, with potassic pyrite recording the highest Cu concentrations (559–7256 ppm, mean 2302 ppm) and chlorite–sericite pyrite containing the lowest Au contents (0.01–0.59 ppm, mean 0.10 ppm). Gold mineralization occurs as native gold exsolved from chalcopyrite, and the markedly low Au concentrations in chlorite–sericite pyrite (0.01–0.59 ppm, mean 0.10 ppm) demonstrate that gold exsolution was largely completed during the first, high-temperature magmatic-hydrothermal stage. Collectively, these results establish a detailed geochemical framework linking sulfide composition to specific hydrothermal stages, providing new constraints on the processes of porphyry copper–gold mineralization in a collisional setting. Full article
17 pages, 9069 KB  
Article
Utilizing Hydrochemistry and Multiple Isotopes to Identify the Accumulation Mechanism of Nitrate in the Yangtze River Basin
by Xiaofeng Liu, Shanshan Xi, Fazhi Xie, Jingjing Yu and Tianzhao Geng
Water 2026, 18(9), 1081; https://doi.org/10.3390/w18091081 - 30 Apr 2026
Viewed by 36
Abstract
The Yangtze River, the largest river system in Asia, continues to receive substantial nitrogen loads despite the implementation of management measures. Within this vast and complex system, the spatial patterns and drivers of key nitrogen transformation processes, such as nitrification and denitrification, remain [...] Read more.
The Yangtze River, the largest river system in Asia, continues to receive substantial nitrogen loads despite the implementation of management measures. Within this vast and complex system, the spatial patterns and drivers of key nitrogen transformation processes, such as nitrification and denitrification, remain poorly constrained. In particular, systematic isotopic evidence from studies spanning the entire upstream–midstream–downstream continuum remains scarce. This study integrates multiple isotopes (δ15N-NO3, δ18O-NO3, δ15N-NH4+) with hydrochemical techniques to elucidate the dominant controls on nitrogen transport and transformation and their spatial heterogeneity across the Yangtze River Basin. Results indicate that dissolved inorganic nitrogen (DIN) is the dominant form of nitrogen pollution in the basin. NO3 concentrations exhibited significant spatial variability, following the pattern downstream (2.86 mg/L) > upstream (1.83 mg/L) > midstream (1.75 mg/L). Isotopic signatures revealed that nitrification is the dominant process controlling the formation and transformation of NO3 throughout the basin. Most δ18O-NO3 values (−5.20‰ to +12.78‰) fell within or close to the theoretical range for nitrification, and a strong positive correlation was observed between δ15N-NO3 and δ15N-NH4+ (R2 = 0.72, p < 0.01), collectively confirming that the conversion of NH4+ to NO3 is the primary pathway. Conversely, denitrification was significantly suppressed under the prevailing high dissolved oxygen conditions (mean 9.78 ± 2.46 mg/L), as further evidenced by the lack of a significant correlation between δ15N-NO3 and ln(NO3). Furthermore, preferential assimilation of NH4+ by phytoplankton reduced the efficiency of nitrate removal via biological assimilation and influenced isotopic composition. These findings provide a scientific basis for identifying priority nitrogen sources and optimizing targeted nitrogen management strategies in the Yangtze River Basin. Full article
(This article belongs to the Section Water Quality and Contamination)
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17 pages, 5025 KB  
Article
The Interaction Between Groundwater and Surface Water in the Southern Sector of the Sabatini Mountains Hydrogeological Structure (Central Italy) Using a Comprehensive Hydrogeological and Geochemical Approach
by Gianmarco Mondati, Martina Mattia, Roberto Mazza, Paola Tuccimei, Cristina Di Salvo, Mauro Brilli and Francesca Giustini
Water 2026, 18(9), 1066; https://doi.org/10.3390/w18091066 - 29 Apr 2026
Viewed by 177
Abstract
Groundwater–surface water interactions in volcanic hydrogeological systems represent a key process in river dynamics and were preliminarily investigated along a river draining the southern sector of the Sabatini Mountains (central Italy) using an integrated hydrogeological and geochemical approach. Serial discharge measurements, combined with [...] Read more.
Groundwater–surface water interactions in volcanic hydrogeological systems represent a key process in river dynamics and were preliminarily investigated along a river draining the southern sector of the Sabatini Mountains (central Italy) using an integrated hydrogeological and geochemical approach. Serial discharge measurements, combined with physico-chemical parameters, major ions, stable oxygen isotopes, and radon analyses, reveal marked spatial variability in river–aquifer exchanges along distinct river reaches. The Arrone River exhibits clear differences between upstream, intermediate, and downstream sections, reflecting the relative influence of localized anthropogenic inputs, diffuse groundwater discharge from the volcanic aquifer, and subsurface flow contributions. Upstream reaches are characterized by pronounced modifications in discharge and chemistry, whereas intermediate and downstream reaches show progressive groundwater influence, resulting in distinct geochemical signatures and changes in water quality. Correlation and cluster analyses identify reach-specific processes controlling water composition and support the recognition of gaining and mixed river conditions under varying hydrological regimes. These results constrain a conceptual model in which river behavior is governed by spatially heterogeneous groundwater inflows, modulated by seasonal discharge dynamics and local human pressures. This study highlights the importance of reach-scale investigations for understanding SW–GW interactions in volcanic settings and provides transferable insights relevant to groundwater-dependent river systems. Full article
17 pages, 4528 KB  
Article
Cross-Reaction Products from Mixed Volatile Organic Compound Oxidation: Evidence from Isotope-Labeled Toluene and α-Pinene Secondary Organic Aerosol
by Hao Jiang, Quanfu He, Bin Jiang and Xiang Ding
Atmosphere 2026, 17(5), 451; https://doi.org/10.3390/atmos17050451 - 29 Apr 2026
Viewed by 179
Abstract
Cross-reactions between peroxy radicals (RO2) derived from different volatile organic compound (VOC) precursors have been proposed as an important pathway during atmospheric oxidation. However, direct molecular evidence has been limited. In this study, α-pinene and fully deuterated toluene (d8-toluene) were oxidized [...] Read more.
Cross-reactions between peroxy radicals (RO2) derived from different volatile organic compound (VOC) precursors have been proposed as an important pathway during atmospheric oxidation. However, direct molecular evidence has been limited. In this study, α-pinene and fully deuterated toluene (d8-toluene) were oxidized separately and as a mixture in a potential aerosol mass (PAM) flow reactor, and the resulting secondary organic aerosol (SOA) was characterized by a high-resolution mass spectrometer (ESI FT-ICR-MS). A constrained chemical mass balance (CMB) model attributed 82.9% of the mixed-SOA signal to single-precursor sources (66.5% α-pinene, 16.4% d8-toluene), leaving a 17.1% signal-based residual fraction unexplained by linear mixing. Among 2450 residual molecular formulas exclusive to the mixed-SOA, 1858 were identified as cross-reaction candidates, with carbon, oxygen, and double bond equivalents (DBE) distributions consistent with RO2-RO2 cross-reactions between toluene- and α-pinene-derived fragments. We also identified representative monomer-dimer pairs, where one monomer corresponded to a known α-pinene oxidation product, while the other matched a primary oxidation product of d8-toluene oxidation based on the Master Chemical Mechanism (MCM), providing strong molecular-level evidence for RO2-RO2 cross-reactions. Our findings demonstrate that the mixed VOCs generate unique SOA products that extend beyond simple additive chemistry, with implications for SOA yield parameterizations and chemical transport models. Full article
(This article belongs to the Section Aerosols)
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13 pages, 4205 KB  
Article
Development and First-in-Human Translation of Hyperpolarized [1-13C]Alpha-Ketoglutarate MR Spectroscopy in the Brain
by Yaewon Kim, Duy Dang, James Slater, Andrew Riselli, Donghyun Hong, Jeremy W. Gordon, Susan M. Chang, Yan Li, Javier E. Villanueva-Meyer, Adam W. Autry, Evelyn Escobar, Stacy Andosca, Hsin-Yu Chen, Chou T. Tan, Chris Suszczynski, Sri Maddali, Robert A. Bok and Daniel B. Vigneron
Sensors 2026, 26(9), 2753; https://doi.org/10.3390/s26092753 - 29 Apr 2026
Viewed by 138
Abstract
Alpha-ketoglutarate (aKG) is a central intermediate of cerebral energy metabolism and a precursor for glutamate synthesis in the brain. Alterations in aKG metabolism occur in pathological contexts, including isocitrate dehydrogenase (IDH) mutant astrocytomas and oligodendrogliomas, in which mutant IDH converts aKG to the [...] Read more.
Alpha-ketoglutarate (aKG) is a central intermediate of cerebral energy metabolism and a precursor for glutamate synthesis in the brain. Alterations in aKG metabolism occur in pathological contexts, including isocitrate dehydrogenase (IDH) mutant astrocytomas and oligodendrogliomas, in which mutant IDH converts aKG to the oncometabolite 2-hydroxyglutarate. Given its central role in brain metabolism, non-invasive interrogation of aKG-dependent metabolic flux is needed. Hyperpolarized (HP) 13C MR enables real-time visualization of metabolic conversion by transiently enhancing signal intensity by several orders of magnitude. Leveraging this approach, we report the first-in-human feasibility and safety study of HP [1-13C]aKG MR spectroscopy in the healthy brain (n = 3). A standard operating procedure (SOP) was developed for sterile [1-13C]aKG dose production, achieving reproducible polarization levels averaging 30.5 ± 2.2%. Following intravenous administration, time-resolved 13C spectra in healthy volunteers demonstrated the detection of HP aKG resonance and a measurable downstream glutamate signal, consistent across repeat acquisitions, with a delayed temporal profile relative to aKG observed in a representative dataset. Although performed in healthy volunteers, these results establish feasibility for HP [1-13C]aKG metabolic imaging to open a new window into normal and pathological brain cellular metabolism. Full article
(This article belongs to the Special Issue Advances in Biosensing and BioMEMS for Biomedical Engineering)
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7 pages, 264 KB  
Article
I-Process Nucleosynthesis in AM CVn Systems
by Luciano Piersanti, Diego Vescovi, Sergio Cristallo, Lev R. Yungelson, Eduardo Bravo, Inmaculada Dominguez and Alexandre G. Kuranov
Galaxies 2026, 14(3), 38; https://doi.org/10.3390/galaxies14030038 - 29 Apr 2026
Viewed by 122
Abstract
We investigate nucleosynthesis during very strong, non-dynamical recurrent He-flashes that are expected to occur in close binary systems hosting a carbon–oxygen white dwarf and a type-B subdwarf companion. In these systems, due to gravitational wave emissions, the subdwarf star is expected to fill [...] Read more.
We investigate nucleosynthesis during very strong, non-dynamical recurrent He-flashes that are expected to occur in close binary systems hosting a carbon–oxygen white dwarf and a type-B subdwarf companion. In these systems, due to gravitational wave emissions, the subdwarf star is expected to fill its Roche lobe on a short timescale, resulting in mass transfer onto the companion. As accreted matter also deposits angular momentum, the external layers of the accretor begin to rotate very fast. So, dynamical He burning is avoided, and the WD instead experiences recurrent strong He flashes, which secularly reduce its mass. We consider the PTF J2238+743015.1 system as representative of the whole class of similar objects and compute its evolution by coupling our evolutionary code with a full nuclear network, including isotopes with a lifetime longer than 0.8 s. We find that during He-flash episodes, the delivered neutron flux is typical for the i-process nucleosynthesis, even if it is available for a very short time (1–10 h). As a consequence, only weak s-process nucleosynthesis takes place. The nucleosynthetic path in the ejected matter is quite similar to that of supernovae descending from massive stars. However, due to the rarity of these systems, as well as to the small amount of matter ejected during the He-flashes phase, their contribution to the evolution of the interstellar medium is negligible. Full article
(This article belongs to the Special Issue Neutron Capture Processes in the Universe)
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16 pages, 6350 KB  
Article
Transcriptome Analysis Revealed the Mechanism of Nitrate Absorption in Tea Plants
by Weiwei Deng, Qiangqiang Xiong, Kang Wei, Yongxin Wang and Liyuan Wang
Plants 2026, 15(9), 1352; https://doi.org/10.3390/plants15091352 - 28 Apr 2026
Viewed by 122
Abstract
Nitrate (NO3) serves as a critical nitrogen source and signaling molecule essential for its growth and quality formation. Although substantial genetic variation in nitrogen use efficiency (NUE) has been documented among tea cultivars, a systematic characterization of nitrate (NO3 [...] Read more.
Nitrate (NO3) serves as a critical nitrogen source and signaling molecule essential for its growth and quality formation. Although substantial genetic variation in nitrogen use efficiency (NUE) has been documented among tea cultivars, a systematic characterization of nitrate (NO3) absorption kinetics and the associated genome-wide transcriptional regulatory networks across varying nitrate concentrations remains lacking. This study employed 15N isotope labeling and transcriptome sequencing to systematically analyze the absorption characteristics and molecular response mechanisms of the cultivars ‘Longjing 43’ and ‘Zhongming 6 hao’ under varying NO3 concentrations. Results revealed significant differentiation in absorption strategies: ‘Zhongming 6 hao’ exhibited a significantly higher absorption rate at low concentrations, whereas ‘Longjing 43’ demonstrated enhanced performance at high concentrations. Transcriptome analysis indicated that both cultivars shared coordinated regulation of ‘photosynthesis’ and ‘nitrogen metabolism’ pathways. Furthermore, 14 nitrogen metabolism genes and 64 differentially expressed transcription factors (including MYB, NAC, and LBD families) were identified. Specifically, the CsNiR gene (encoding nitrite reductase) was functionally validated; silencing of CsNiR significantly reduced nitrite reductase activity, confirming its positive regulatory role. This study provided a theoretical framework and key candidate genes for breeding nitrogen-use-efficient varieties, which is essential for sustainable tea production. Full article
(This article belongs to the Special Issue Genetic Breeding and Quality Improvement of Tea)
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Article
A Triple-Resonance NMR Strategy for the Selective Detection of NAD+ and NADH Derived from a 13C/15N-Nicotinamide Riboside Probe in the Liver Extracts of Mice
by Hiroki Shimada, Yusei Shinohara, Yoshihiro Uto and Hisatsugu Yamada
Sensors 2026, 26(9), 2714; https://doi.org/10.3390/s26092714 - 28 Apr 2026
Viewed by 167
Abstract
Alterations in the ratio of oxidized and reduced nicotinamide adenine dinucleotide (NAD+/NADH) reflect the intracellular redox state and have been implicated in a broad spectrum of pathological conditions, including neurogenetic disorders, heart failure, and liver diseases. In the present study, we [...] Read more.
Alterations in the ratio of oxidized and reduced nicotinamide adenine dinucleotide (NAD+/NADH) reflect the intracellular redox state and have been implicated in a broad spectrum of pathological conditions, including neurogenetic disorders, heart failure, and liver diseases. In the present study, we demonstrate the selective detection of probe-derived NAD+ and NADH signals in mouse liver extracts by means of a triple-resonance nuclear magnetic resonance (NMR) spectroscopy technique. We prepared 13C/15N-enriched nicotinamide riboside (13C/15N-NR), which undergoes enzymatic conversion to NAD+ and NADH in the liver, and detected these labeled metabolites by 1H–{13C–15N} triple-resonance NMR measurements. This study provides a methodological proof-of-concept for the selective detection of NAD-related signals derived from a stable-isotope labeled probe in mouse liver extracts. Full article
(This article belongs to the Section Biosensors)
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