Impact of a Low Severity Fire on Soil Organic Carbon and Nitrogen

Slash and burn practices are widely used around the globe with different degrees of success which are mostly related to the impact of fire on soil properties. In Japan slash and burn practises, known as Yakihata, have a long history and are still used in Yamagata Prefecture today. The purpose of this study was to determine the impact of a low severity controlled fire underneath Japanese cedar (Cryptomeria japonica) on brown forest soil (Cambisol). Japanese Cedar is the dominant species among plantations in Japan. We measured organic carbon and nitrogen content as well as changes in carbon (δ13C) and nitrogen (δ15N) stable isotope composition in a steep west facing slope under heavy precipitation (~2600 mm/a) and heavy snowfall (~3 to 4 m/a). The accumulation of Ctotal and Ntotal at the bottom of the slopes was remarkably higher at the slash and burned site than in the control forest site. After slash and burn δ15N isotopes in the slope in general became significantly lighter than in the control forest while the δ13C did not show any significant difference between the two sites except at the bottom of the slopes where δ13C was heavier in the forest. The results show that Ctotal and Ntotal values as well as the isotopes ratios of C and N change with decreasing elevation in the forest as well as in the burned site being consistent with leaching and erosion. The changes in soil nitrogen and carbon isotopes at the bottom of the slope appear to be related to the transport of material with different isotopic composition from the upper slope. The effect of the low severity fire (as part of the slash and burn practice) on soil organic carbon and nitrogen movement was enhanced by the steepness of the slopes and the high precipitation of Shonai region

Evaluation of the effect of the 2011 Tsunami on coastal forests by means of multiple isotopic analyses of tree-rings

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Characterization of the In Vitro and In Vivo Efficacy of Baloxavir Marboxil against H5 Highly Pathogenic Avian Influenza Virus Infection

Human infections caused by the H5 highly pathogenic avian influenza virus (HPAIV) sporadically threaten public health. The susceptibility of HPAIVs to baloxavir acid (BXA), a new class of inhibitors for the influenza virus cap-dependent endonuclease, has been confirmed in vitro, but it has not yet been fully characterized. Here, the efficacy of BXA against HPAIVs, including recent H5N8 variants, was assessed in vitro. The antiviral efficacy of baloxavir marboxil (BXM) in H5N1 virus-infected mice was also investigated. BXA exhibited similar in vitro activities against H5N1, H5N6, and H5N8 variants tested in comparison with seasonal and other zoonotic strains. Compared with oseltamivir phosphate (OSP), BXM monotherapy in mice infected with the H5N1 HPAIV clinical isolate, the A/Hong Kong/483/1997 strain, also caused a significant reduction in viral titers in the lungs, brains, and kidneys, thereby preventing acute lung inflammation and reducing mortality. Furthermore, compared with BXM or OSP monotherapy, combination treatments with BXM and OSP using a 48-h delayed treatment model showed a more potent effect on viral replication in the organs, accompanied by improved survival. In conclusion, BXM has a potent antiviral efficacy against H5 HPAIV infections

Identification of cap-dependent endonuclease inhibitors with broad-spectrum activity against bunyaviruses

Viral hemorrhagic fevers caused by members of the order Bunyavirales comprise endemic and emerging human infections that are significant public health concerns. Despite the disease severity, there are few therapeutic options available, and therefore effective antiviral drugs are urgently needed to reduce disease burdens. Bunyaviruses, like influenza viruses (IFVs), possess a cap-dependent endonuclease (CEN) that mediates the critical cap-snatching step of viral RNA transcription. We screened compounds from our CEN inhibitor (CENi) library and identified specific structural compounds that are 100 to 1,000 times more active in vitro than ribavirin against bunyaviruses, including Lassa virus, lymphocytic choriomeningitis virus (LCMV), and Junin virus. To investigate their inhibitory mechanism of action, drug-resistant viruses were selected in culture. Whole-genome sequencing revealed that amino acid substitutions in the CEN region of drug-resistant viruses were located in similar positions as those of the CEN α3-helix loop of IFVs derived under drug selection. Thus, our studies suggest that CENi compounds inhibit both bunyavirus and IFV replication in a mechanistically similar manner. Structural analysis revealed that the side chain of the carboxyl group at the seventh position of the main structure of the compound was essential for the high antiviral activity against bunyaviruses. In LCMV-infected mice, the compounds significantly decreased blood viral load, suppressed symptoms such as thrombocytopenia and hepatic dysfunction, and improved survival rates. These data suggest a potential broad-spectrum clinical utility of CENis for the treatment of both severe influenza and hemorrhagic diseases caused by bunyaviruses