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Saline lakes are experiencing significant changes in salinity and organic matter content due to climate change. However, the specific impacts of these environmental changes on the production processes of nitrous oxide (NO)-particularly nitrification and denitrification-in saline lake sediments are still poorly understood, leading to significant uncertainty in current estimates of greenhouse gas (GHG) emission from these ecosystems. Here, we employed N-isotope labeling, functional gene quantification, and structural equation modeling to elucidate NO production pathways and rates in surface sediments along a salinity gradient (0.7-149.3 g/L) within Qinghai-Tibet Plateau (QTP) lakes undergoing rapid desalination and organic carbon enrichment. The results identified saline lake sediments as hotspots for NO production, with nitrification contributing an average of 43.51 % to NO flux and reaching up to 91.73 % in specific high-salinity habitats, highlighting its previously underestimated significance. Salinity was found to limit NO production through both nitrifying and denitrifying processes in lake sediments, although dissolved organic carbon (DOC) in the sediment could counteract the limitation caused by salt. Low-salinity systems (<35 g/L) exhibited predominant salinity-related inhibition of denitrification, whereas high-salinity systems (>35 g/L) displayed DOC-mediated counteraction of salinity stress, stimulating both denitrification and heterotrophic nitrification through alterations in microbial community structure (e.g., reflected by nir/nos ratios). This finding illustrates that climate-driven freshening and organic carbon loading synergistically exacerbate NO emissions in saline lakes. While denitrification remains dominant, heterotrophic nitrification pathways are increasingly significant under saline conditions. This highlights susceptibility of cryosphere-affected ecosystems to hydrological disturbances, and emphasizes the necessity of refining global GHG inventories by incorporating context-dependent NO source partitioning.
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http://dx.doi.org/10.1016/j.watres.2025.124111 | DOI Listing |
Environ Monit Assess
September 2025
Institute of Environmental Studies, Kurukshetra University, Kurukshetra, Haryana, 136119, India.
India produces an estimated 6.38 million tons of surplus sugarcane trash annually. When burned in fields, this trash emits approximately 12,948 kg CO equivalent greenhouse gases per hectare and causes nutrient losses (41 kg ha nitrogen, 5.
View Article and Find Full Text PDFJ Org Chem
September 2025
Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Halogen atom transfer (XAT) is a pivotal strategy for generating carbon-centered radicals in organic chemistry, yet current methodologies often rely on toxic tin-based reagents or inefficient organosilanes. This study explores diazaphosphinyl (-heterocyclic phosphinyl, NHP) radicals as new halogen abstractors, leveraging their nucleophilic and halophilic properties. We synthesized a series of NHP-X (X = Cl or Br) compounds, systematically determining their P-X bond energies and related redox potentials.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway.
LiNiMnO (LNMO) is a promising material for the cathode of lithium-ion batteries (LiBs); however, its high operating voltage causes stability issues when used with carbonate battery electrolytes. Ionic liquids are a viable alternative to conventional carbonate solvents due to their thermal stability and electrochemical window. This work reports the performance of LNMO/Li half cells with an ionic liquid electrolyte (ILE) composed of 0.
View Article and Find Full Text PDFAppl Environ Microbiol
September 2025
Biofuels Institute, School of Emergency Management, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang, Jiangsu, PR China.
is a thermophilic acetogenic bacterium capable of thriving at elevated temperatures up to 66°C. It metabolizes carbohydrates such as glucose, mannose, and fructose and can also grow lithotrophically utilizing hydrogen (H) and carbon dioxide (CO) or carbon monoxide (CO), with acetate serving as its main product. A simple and efficient genome editing system for would not only facilitate the understanding of the physiological function of enzymes involved in energy and carbon metabolism but also enable metabolic engineering.
View Article and Find Full Text PDFChemSusChem
September 2025
Institute of Organic Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Organic battery electrode materials represent a sustainable alternative compared to most inorganic electrodes, yet challenges persist regarding their energy density and cycling stability. In this work, a new organic electrode material is described, which is obtained via ionothermal polymerization of low-cost starting materials, melem (2,5,8-triamino-tri-s-triazine) and perylenetetracarboxylic dianhydride (PTCDA). The resulting networked polymer Melem-PDI exhibits favorable thermal and electrochemical properties, prompting investigation into its performance as a positive electrode material in rechargeable lithium and magnesium batteries.
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