In this study, we investigated the changes in the distribution and regulation of endogenous hormones in Phyllostachys edulis ‘Pachyloen’ during bamboo shooting. Enzyme-linked immunosorbent assay was used to measure the mass fractions of indole-3-acetic acid (IAA), gibberellic acid (GA), zeatin riboside (ZR), and abscisic acid (ABA) in rhizomes, shoots, and maternal bamboo organs during shoot sprouting, shoot growth, and new-bamboo formation. Measurements were compared among bamboo parts and developmental periods. The overall mass fractions of IAA and ABA were significantly higher than those of ZR and GA, driven by differences among bamboo parts and developmental periods. The abundance of each endogenous hormone varied among bamboo parts and developmental periods. During bamboo shooting, ABA had the highest mass fraction in all bamboo parts sampled, followed by IAA, GA, and ZR. Among bamboo parts, rhizomes had more IAA, ZR, and GA than the other parts, but significantly less ABA. Winter shoots had higher ZR: IAA and GA: IAA ratios than rhizomes and maternal bamboo organs. During shoot growth, ABA was the most abundant hormone in rhizomes and maternal bamboo organs, followed by IAA, ZR, and GA. In contrast, IAA was the most abundant hormone in spring shoots, followed by ABA, ZR, and GA. Maternal bamboo organs had a significantly higher ZR: GA ratio, and significantly lower IAA: ABA, ZR: ABA, and GA: ABA ratios than rhizomes. Spring shoots had significantly higher IAA: ABA, ZR: ABA, and GA: ABA ratios than rhizomes and maternal bamboo organs; significantly higher ZR mass fractions, and ZR: GA and ZR: IAA ratios and significantly lower ABA mass fractions than rhizomes; and significantly higher GA: IAA ratio than maternal bamboo organs. During new-bamboo formation, ABA was the most abundant hormone in rhizomes, winter shoots, and maternal bamboo organs, followed by IAA, ZR, and GA. Maternal bamboo organs had significantly lower IAA mass fractions and significantly higher ABA mass fractions than rhizomes and new bamboo tissue. IAA and ABA abundances exhibited an inverse relationship in rhizomes and maternal bamboo organs. GA: ABA and GA: IAA ratios decreased gradually and other hormone ratios exhibited parabolic trends over the bamboo-shooting period, with the highest ratios observed in new bamboo tissues. Overall, the coordination or antagonism among endogenous hormones plays a key regulatory role in bamboo shoot growth. The formation of thick walls in P. edulis ‘Pachyloen’, one of its major traits, may be partially attributed to the relatively high IAA and ZR and low GA mass fractions.

GRAS family is one of plant specific transcription factors and plays diverse roles in the regulation of plant growth and development as well as in the plant disease resistance and abiotic stress responses. However, the investigation of GRAS family and multi-tissue gene expression profiles still remains unavailable in bamboo (Phyllostachys edulis). Here, we applied RNA-Seq analysis to monitor global transcriptional changes and investigate expression patterns in the five tissues of Ph. edulis, and analyzed a large-scale transcriptional events and patterns. Moreover, the tissue-specific genes and DEGs in different tissues were detected. For example, DEGs in panicle and leaf tissues were abundant in photosynthesis, glutathione, porphyrin and chlorophyll metabolism, whereas those in shoot and rhizome were majority in glycerophospholipid metabolism. In the portion of Ph. edulis GRAS (PeGRAS) analyses, we performed the analysis of phylogenetic, gene structure, conserved motifs, and analyzed the expression profiles of PeGRASs in response to high light and made a co-expression analysis. Additionally, the expression profiles of PeGRASs were validated using quantitative real-time PCR. Thus, PeGRASs based on dynamics profiles of gene expression is helpful in uncovering the specific biological functions which might be of critical values for bioengineering to improve bamboo breeding in future.

This study investigates the dynamics of soil CO₂ emissions during the cover period of Phyllostachys violascens and the impact of different cover measures, aiming to provide references for reducing the environmental effects of bamboo cover. An L₂₇ (9¹³) orthogonal experimental design was employed, setting the following variables: (1) heating materials: chicken manure, straw cake, and wheat ash; (2) thickness of husk layer: 15 cm, 25 cm, and 35 cm; (3) soil moisture levels before covering: moisture to 10 cm, 15 cm, and 20 cm. The soil CO₂ emission rate showed a unimodal curve, with a significant overall increase during the cover period. Throughout the entire cover period, the average soil CO₂ emission rate (25.39 μmol·m⁻²·s⁻¹) was 5.1 times higher than that of the uncovered Lei bamboo forest (5.02 μmol·m⁻²·s⁻¹) during the same period. Thicker husk layers (25 cm and 35 cm) corresponded to higher soil CO₂ emission rates, with significant differences noted among the thicknesses. When the soil was moist to 10 cm, the CO₂ emission rate was highest (62.51 μmol·m⁻²·s⁻¹); moisture to 15 cm and 20 cm resulted in significantly lower emission rates. Chicken manure produced the highest peak CO₂ emissions in the third week, at 70.64 μmol·m⁻²·s⁻¹, while straw cake and wheat ash reached their peaks in the fifth week, at 66.56 μmol·m⁻²·s⁻¹ and 57.58 μmol·m⁻²·s⁻¹, respectively. The interactions between the three factors (heating materials, husk layer thickness, and moisture levels) significantly affected the soil CO₂ emission rates. By optimally configuring these factors, CO₂ emissions can be regulated. This study recommends using wheat ash or straw cake as heating materials, combined with a 25 cm husk layer thickness, and moistening the soil to 15 cm before covering. This approach effectively reduces the peak and total soil CO₂ emissions while ensuring suitable soil temperatures for the growth of bamboo shoots in spring. This research provides a scientific basis for the environmental management of bamboo forests, aiding in the optimization of covering measures to achieve low-carbon and sustainable bamboo management.