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Large-scale afforestation is considered an effective measure to mitigate climate change. However, due to the differences in the properties of soil organic carbon (SOC), the dynamic response of SOC to large-scale afforestation remained unclear. Therefore, we conducted paired sampling (farmland and afforestation) in plantation areas across northern China to evaluate the relationship between SOC stability and SOC increments (ΔSOC) resulting from afforestation. Our findings indicated that SOC-unstable soil supported greater carbon increments through afforestation, but at the expense of reduced SOC stability after afforestation. Additionally, we observed that this relationship exhibited geographical characteristics, with SOC-unstable soil demonstrating a stronger capacity to enhance ΔSOC at higher latitudes, particularly in the topsoil. This is primarily attributed to the fact that higher latitudes and colder climates enhance the contribution of particulate organic carbon to ΔSOC and weaken the regulatory effect of SOC chemical composition (carboxyl and aromatic carbon) on SOC stability after afforestation. These findings underscore the importance of incorporating pre-afforestation SOC stability to accurately predict soil carbon-afforestation feedback.
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http://dx.doi.org/10.1016/j.jenvman.2025.125032 | DOI Listing |
J Am Chem Soc
September 2025
Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24060, United States.
Recently photoinduced dynamic ligation in a metal-organic frameworks (MOFs) was reported, where a long-lived charge-transfer excited state (ca. 30 μs) featuring partial dissociation between the carboxylate linker and metal-based node was probed by time-resolved infrared (TRIR) spectroscopy. The study offers a new mechanistic perspective to evaluate the potential contribution from the excited state molecular configuration to the performance of MOF photocatalysts.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
Among the different types of HIV-1 maturation inhibitors, those that stabilize the junction between the capsid protein C-terminal domain (CA) and the spacer peptide 1 (SP1) within the immature Gag lattice are promising candidates for antiretroviral therapies. Here, we report the atomic-resolution structure of CA-SP1 assemblies with the small-molecule maturation inhibitor PF-46396 and the assembly cofactor inositol hexakisphosphate (IP6), determined by magic angle spinning (MAS) NMR spectroscopy. Our results reveal that although the two PF-46396 enantiomers exhibit distinct binding modes, they both possess similar anti-HIV potency.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, Boston University, Boston, Massachusetts 02215, United States.
Two-dimensional (2D) materials offer a valuable platform for manipulating and studying chemical reactions at the atomic level, owing to the ease of controlling their microscopic structure at the nanometer scale. While extensive research has been conducted on the structure-dependent chemical activity of 2D materials, the influence of structural transformation during the reaction has remained largely unexplored. In this work, we report the layer-dependent chemical reactivity of MoS during a nitridation atomic substitution reaction and attribute it to the rearrangement of Mo atoms.
View Article and Find Full Text PDFJ Am Soc Nephrol
September 2025
Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Background: Genetic modifiers are believed to play an important role in the onset and severity of polycystic kidney disease (PKD), but identifying these modifiers has been challenging due to the lack of effective methodologies.
Methods: We generated zebrafish mutants of IFT140, a skeletal ciliopathy gene and newly identified autosomal dominant PKD (ADPKD) gene, to examine skeletal development and kidney cyst formation in larval and juvenile mutants. Additionally, we utilized ift140 crispants, generated through efficient microhomology-mediated end joining (MMEJ)-based genome editing, to compare phenotypes with mutants and conduct a pilot genetic modifier screen.
J Am Chem Soc
September 2025
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) State Key Laboratory of Advanced Chemical Power Sources, College of Chemistry, Nankai University, Tianjin 300071, China.
Developing cost-effective spinel oxide catalysts with both high oxygen evolution reaction (OER) activity and stability is crucial for advancing sustainable clean energy conversion. However, practical applications are often hindered by the activity limitations inherent in the adsorbate evolution mechanism (AEM) and the stability limitations associated with the lattice oxygen mechanism (LOM). Herein, we demonstrate structural changes induced by phase transformation in CoMn spinel oxides, which yield more active octahedral sites with shortened intersite distance.
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