Effects of landscape plant species and concentration of sewage sludge compost on plant growth, nutrient uptake, and heavy metal removal.

Landscape plants have great potentials in heavy metals (HMs) removal as sewage sludge compost (SSC) is increasingly used in urban forestry. We hypothesize that woody plants might perform better in HMs phytoremediation because they have greater biomass and deeper roots than herbaceous plants. We tested the differences in growth responses and HMs phytoremediation among several herbaceous and woody species growing under different SSC concentrations through pot experiments. The mixing percentage of SSC with soil at 0%, 15%, 30%, 60, and 100% were used as growth substrate for three woody (Ficus altissima Bl., Neolamarckia cadamba (Roxb.) Bosser, and Bischofia javanica Bl.) and two herbaceous (Alocasia macrorrhiza (L.) G. Don and Dianella ensifolia (L.) DC) plants. Results showed that the biomass, relative growth rate, and nutrient uptake for all plants increased significantly at each SSC concentration compared to the control; woody plants had higher biomass and nutrient use efficiency than herbaceous plants. All plants growing in SSC-amended soils accumulated appreciable amounts of HMs and reduced the contents of HMs present in the substrates. The woody plants were generally more effective than herbaceous plants in potentials of HMs phytoextraction, but A. macrorrhiza showed higher bioconcentration and translocation of Cu and Zn and D. ensifolia had higher bioconcentration and translocation of Cd than woody plants. The optimal application concentrations were 30% or less for woody plants and 15% for herbaceous plants for plant growth and ecological risk control, respectively. Intercropping suitable woody and herbaceous landscape plants in urban forestry might have promising potentials to minimize the ecological risks in the phytoremediation of SSC.

Synthesis of phosphaisocoumarin amidates via DIBAL-H-mediated selective amidation of phosphaisocoumarin esters.

A series of phosphaisocoumarin amidates were synthesized for the first time via DIBAL-H-mediated direct amidation of phosphaisocoumarin esters under mild conditions in good to excellent yields. The present reaction showed high selectivity. In each case, the phostone ring was intact and only the exocyclic ethoxy group was amidated. A plausible mechanism of the reaction was provided.