Abstract. The Tibetan Plateau (TP) has the largest areas of permafrost terrain in the mid-and low-latitude regions of the world. Some permafrost distribution maps have been compiled but, due to limited data sources, ambiguous criteria, inadequate validation, and deficiency of high-quality spatial data sets, there is high uncertainty in the mapping of the permafrost distribution on the TP. We generated a new permafrost map based on freezing and thawing indices from modified Moderate Resolution Imaging Spectroradiometer (MODIS) land surface temperatures (LSTs) and validated this map using various ground-based data sets. The soil thermal properties of five soil types across the TP were estimated according to an empirical equation and soil properties (moisture content and bulk density). The temperature at the top of permafrost (TTOP) model was applied to simulate the permafrost distribution. Permafrost, seasonally frozen ground, and unfrozen ground covered areas of 1.06 × 10 6 km 2 (0.97-1.15 × 10 6 km 2 , 90 % confidence interval) (40 %), 1.46 × 10 6 (56 %), and 0.03 × 10 6 km 2 (1 %), respectively, excluding glaciers and lakes. Ground-based observations of the permafrost distribution across the five investigated regions (IRs, located in the transition zones of the permafrost and seasonally frozen ground) and three highway transects (across the entire permafrost regions from north to south) were used to validate the model. Validation results showed that the kappa coefficient varied from 0.38 to 0.78 with a mean of 0.57 for the five IRs and 0.62 to 0.74 with a mean of 0.68 within the three transects. Compared with earlier studies, the TTOP modelling results show greater accuracy. The results provide more detailed information on the permafrost distribution and basic data for use in future research on the Tibetan Plateau permafrost.

We have developed a genetics-based phytoremediation strategy for arsenic in which the oxyanion arsenate is transported aboveground, reduced to arsenite, and sequestered in thiol-peptide complexes. The Escherichia coli arsC gene encodes arsenate reductase (ArsC), which catalyzes the glutathione (GSH)-coupled electrochemical reduction of arsenate to the more toxic arsenite. Arabidopsis thaliana plants transformed with the arsC gene expressed from a light-induced soybean rubisco promoter (SRS1p) strongly express ArsC protein in leaves, but not roots, and were consequently hypersensitive to arsenate. Arabidopsis plants expressing the E. coli gene encoding gamma-glutamylcysteine synthetase (gamma-ECS) from a strong constitutive actin promoter (ACT2p) were moderately tolerant to arsenic compared with wild type. However, plants expressing SRS1p/ArsC and ACT2p/gamma-ECS together showed substantially greater arsenic tolerance than gamma-ECS or wild-type plants. When grown on arsenic, these plants accumulated 4- to 17-fold greater fresh shoot weight and accumulated 2- to 3-fold more arsenic per gram of tissue than wild type or plants expressing gamma-ECS or ArsC alone. This arsenic remediation strategy should be applicable to a wide variety of plant species.

In Saccharomyces cerevisiae, expression of the ACR2 and ACR3 genes confers arsenical resistance. Acr2p is the first identified eukaryotic arsenate reductase. It reduces arsenate to arsenite, which is then extruded from cells by Acr3p. In this study, we demonstrate that ACR2 complemented the arsenate-sensitive phenotype of an arsC deletion in Escherichia coli. ACR2 was cloned into a bacterial expression vector and expressed in E. coli as a C-terminally histidine-tagged protein that was purified by sequential metal chelate affinity and gel filtration chromatography. Acr2p purified as a homodimer of 34 kDa. The purified protein was shown to catalyze the reduction of arsenate to arsenite. Enzymatic activity as a function of arsenate concentration exhibited an apparent positive cooperativity with an apparent Hill coefficient of 2.7. Activity required GSH and glutaredoxin as the source of reducing equivalents. Thioredoxin was unable to support arsenate reduction. However, glutaredoxins from both S. cerevisiae and E. coli were able to serve as reductants. Analysis of grx mutants lacking one or both cysteine residues in the Cys-Pro-Tyr-Cys active site demonstrated that only the N-terminal cysteine residue is essential for arsenate reductase activity. This suggests that during the catalytic cycle, Acr2p forms a mixed disulfide with GSH before being reduced by glutaredoxin to regenerate the active Acr2p reductase.

SummaryTomato fruits were treated by exogenous melatonin. The effect of melatonin on ethylene biosynthesis, ethylene perception, and ethylene signalling may contribute to fruit ripening and quality improvement in tomato.