Search

Drought stress, which often occurs repeatedly across the world, can cause multiple and long-term effects on plant growth. However, the repeated drought–rewatering effects on plant growth remain uncertain. This study was conducted to determine the effects of drought–rewatering cycles on aboveground growth and explore the underlying mechanisms. Perennial ryegrass plants were subjected to three watering regimes: well-watered control (W), two cycles of drought–rewatering (D2R), and one cycle of drought–rewatering (D1R). The results indicated that the D2R treatment increased the tiller number by 40.9% and accumulated 28.3% more aboveground biomass compared with W; whereas the D1R treatment reduced the tiller number by 23.9% and biomass by 42.2% compared to the W treatment. A time-course transcriptome analysis was performed using crown tissues obtained from plants under D2R and W treatments at 14, 17, 30, and 33 days (d). A total number of 2272 differentially expressed genes (DEGs) were identified. In addition, an in-depth weighted gene co-expression network analysis (WGCNA) was carried out to investigate the relationship between RNA-seq data and tiller number. The results indicated that DEGs were enriched in photosynthesis-related pathways and were further supported by chlorophyll content measurements. Moreover, tiller-development-related hub genes were identified in the D2R treatment, including F-box/LRR-repeat MAX2 homolog (D3), homeobox-leucine zipper protein HOX12-like (HOX12), and putative laccase-17 (LAC17). The consistency of RNA-seq and qRT-PCR data were validated by high Pearson’s correlation coefficients ranging from 0.899 to 0.998. This study can provide a new irrigation management strategy that might increase plant biomass with less water consumption. In addition, candidate photosynthesis and hub genes in regulating tiller growth may provide new insights for drought-resistant breeding.

Plants are key components of the terrestrial ecosystem carbon cycle. Atmospheric CO2 is assimilated through photosynthesis and stored in plant biomass and in the soil. The use of turfgrass is expanding due to the increasing human population and urbanization. In this review, we summarize recent carbon sequestration research in turfgrass and compare turfgrass systems to other plant systems. The soil organic carbon (SOC) stored in turfgrass systems is comparable to that in other natural and agricultural systems. Turfgrass systems are generally carbon-neutral or carbon sinks, with the exception of intensively managed areas, such as golf course greens and athletic fields. Turfgrass used in other areas, such as golf course fairways and roughs, parks, and home lawns, has the potential to contribute to carbon sequestration if proper management practices are implemented. High management inputs can increase the biomass productivity of turfgrass but do not guarantee higher SOC compared to low management inputs. Additionally, choosing the appropriate turfgrass species that are well adapted to the local climate and tolerant to stresses can maximize CO2 assimilation and biomass productivity, although other factors, such as soil respiration, can considerably affect SOC. Future research is needed to document the complete carbon footprint, as well as to identify best management practices and appropriate turfgrass species to enhance carbon sequestration in turfgrass systems.

Extensive stolon development and growth are superior traits for rapid establishment as well as post-stress regeneration in stoloniferous grass species. Despite the importance of those stoloniferous traits, the regulation mechanisms of stolon growth and development are largely unknown. The objectives of this research were to elucidate the effects of the reallocation of soluble sugars for energy reserves and endogenous hormone levels for cell differentiation and regeneration in regulating stolon growth of a perennial turfgrass species, creeping bentgrass (Agrostis stolonifera L.). Plants were grown in growth chambers with two CO2 concentrations: ambient CO2 concentration (400 ± 10 µmol mol−1) and elevated CO2 concentration (800 ± 10 µmol mol−1). Elevated CO2 enhanced stolon growth through increasing stolon internode number and internode length in creeping bentgrass, as manifested by the longer total stolon length and greater shoot biomass. The content of glucose, sucrose, and fructose as well as endogenous IAA were accumulated in stolon nodes and internodes but not in leaves or roots under elevated CO2 concentration. These results illustrated that the production and reallocation of soluble sugars to stolons as well as the increased level of IAA in stolon nodes and internodes could contribute to the enhancement of stolon growth under elevated CO2 in creeping bentgrass.