Responses of alpine summit vegetation under climate change in the transition zone between subtropical and tropical humid environment.

Climate change has caused severe impacts on ecosystems and biodiversity globally, especially to vulnerable mountain ecosystems; the summits bear the brunt of such effects. Therefore, six summits in Taiwan were monitored based on a standardized multi-summit approach. We used both statistical downscaling of climate data and vegetation cover data to calculate climate niches to assess the impacts of climate change. Two indicators, thermophilic and moist-philic, were applied to evaluate the overall response of vegetation dynamics. The results revealed that potential evapotranspiration increased significantly and led to a declining tendency in monthly water balance from 2014 to 2019. The general pattern of species richness was a decline. The difference in plant cover among the three surveys showed an inconsistent pattern, although some dominant species expanded, such as the dwarf bamboo Yushania niitakayamensis. The thermophilic indicator showed that species composition had changed so that there were more thermophilic species at the three lowest summits. The moist-philization indicator showed a decline of humid-preferred species in the latest monitoring period. Although total precipitation did not decrease, our results suggest that the variability in precipitation with increased temperature and potential evapotranspiration altered alpine vegetation composition and could endanger vulnerable species in the future.

Mahonia oiwakensis Extract and Its Bioactive Compounds Exert Anti-Inflammatory Activities and VEGF Production Through M2-Macrophagic Polarization and STAT6 Activation.

Macrophages play an indispensable role in the host immune defense. Macrophages can undergo polarization into classically (M1) and alternatively (M2) activated macrophages. M1 macrophages activate immune and inflammatory response, while M2 macrophages are involved in tissue remodeling. Mahonia oiwakensis (Mo) is a herbal medicine in Asia used for its anti-inflammatory and analgesic properties; however, the mechanism is unclear. This study analyzed the effect of Mo extracts and its effects on the polarization of both macrophage RAW264.7 cells and mouse splenic macrophages. Water (Mo-W) and EtOH extracts (Mo-E) did not change the viability of RAW264.7 cells, whereas Mo-E inhibited nitric oxide (NO) production. The major compounds, berberine and palmatine, decreased the viability and NO levels of cells. The secretion of inflammatory cytokines CXCL16, IL-6, L-selectin, MCP1, RANTES, and sTNF-R1 was downregulated, whereas the production of vascular endothelial growth factor (VEGF) was upregulated by Mo-E, berberine, and palmatine treatments. Mo-E, berberine, and palmatine stimulated the expression of macrophage CD68 and M2-type CD204 markers, decreased M1-mediated p-STAT1 and NF-κB, and increased M2-mediated p-STAT6 expression. Similar effects on M2 polarization were also observed in splenic macrophages from mice. In conclusion, Mo-E, berberine, and palmatine modulated macrophages through the suppression of M1-mediated inflammation and the recruitment of M2-mediated VEGF secretion and STAT6 expression.