[Spatial-temporal variation of vegetation water use efficiency and its relationship with climate factors over the Qinghai-Tibet Plateau, China]. / é’è—é«˜åŽŸæ¤è¢«æ°´åˆ†åˆ©ç”¨æ•ˆçŽ‡æ—¶ç©ºå˜åŒ–åŠä¸Žæ°”å€™å› å­çš„å ³ç³».

Water use efficiency (WUE) is an effective index to study the coupling of land carbon and water cycle. The Qinghai-Tibet Plateau is the most important ecological security barrier in China. Understanding the characteristics and mechanism of WUE is important for the carbon cycle and water resources rational utilization in the plateau. Based on MODIS data of gross primary productivity (GPP) and evapotranspiration (ET), we analyzed the spatial-temporal variations of WUE over the Qinghai-Tibet Plateau and the effects of climate factors. The results showed that WUE in the Qinghai-Tibet Plateau had an upward trend under the combined action of GPP and ET during 2001-2020. The southeast and northeast of the Plateau had the highest WUE value, while the central part had the lowest WUE value. WUE of grassland, marsh and alpine vegetation showed an increasing trend, while that of shrub land, broadleaved forest and coniferous forest showed a decreasing trend. There was a significant positive correlation between WUE and annual air temperature, and the sensitivity increased with the increases of air temperature. The relationship between WUE and annual precipitation was non-linear. When precipitation was less than 700 mm, the sensitivity of WUE to precipitation decreased with the increases of precipitation. When precipitation was more than 700 mm, the sensitivity of precipitation increased with the increases of precipitation. However, WUE was negatively correlated with precipitation in more than 75% of regions, and was affected by precipitation in a larger area. In the future, warm and humid climate would lead to a decrease in WUE.

Synthesis of Substituted Piperidines from N,N-Bis[(benzotriazol-1-yl)methyl]amines.

N,N-Bis[(benzotriazol-1-yl)methyl]benzylamines and N,N-bis[(benzotriazol-1-yl)methyl](p-N',N'-dimethylphenyl)amine on reaction with allyltrimethylsilanes yielded substituted piperidines. Other N,N-bis[(benzotriazol-1-yl)methyl]anilines (unsubstituted and p-CH(3), OCH(3), Cl) gave julolidines (2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij] quinoline).

Asymmetric Syntheses of 2-Substituted and 2,5-Disubstituted Pyrrolidines from (3S,5R,7aR)-5-(Benzotriazol-1-yl)-3-phenyl[2,1-b]oxazolopyrrolidine.

Benzotriazole, 2,5-dimethoxytetrahydrofuran, and (S)-phenylglycinol in one step gave 80% of (3S, 5R,7aR)-5-(benzotriazol-1-yl)-3-phenyl-[2,1-b]oxazolopyrrolidine (6), whose crystal structure was confirmed by X-ray crystallography. Novel chiral pyrrolidine synthon 6 reacts with organosilicon (allyltrimethylsilanes and vinyloxytrimethylsilanes), organophosphorus, organozinc, and Grignard reagents to afford chiral 2-substituted and 2,5-disubstituted pyrrolidines.