High summer temperatures increasingly constrain sweet cherry production, yet field-validated assessments of rootstock resilience remain scarce. To fill this gap, this study presents a pioneering multidimensional evaluation of five widely used sweet cherry rootstocks (Gisela 6, Gisela 12, Krymsk 5, Colt, and Lanting) under prolonged natural heat stress. Morphological traits, leaf anatomical characteristics, antioxidant enzyme activities (SOD, CAT, POD), lipid peroxidation (MDA), phytohormones (ABA and JA), and osmotic regulators were assessed. Traits with high coefficients of variation, including POD activity, ABA, JA, and soluble protein content, were identified as sensitive indicators of heat stress. Lanting exhibited the strongest heat tolerance, characterized by thicker leaves, fewer heat-induced lesions, and enhanced antioxidant capacity, whereas Gisela 6 showed severe leaf abscission, elevated MDA and ABA accumulation, and the weakest defense capacity. Correlation analysis indicated that root sucker number was positively associated with SOD activity and soluble sugar content, suggesting a potential role of whole-plant carbon allocation in mitigating oxidative stress. Using the Entropy Weight–TOPSIS model, we provided a robust ranking that identifies Lanting and Colt as superior heat-resilient genotypes. The results provide a field-validated framework that bridges the gap between controlled-environment theory and practical orchard management, offering critical guidance for expanding sweet cherry cultivation into high-temperature regions.

Waterlogging stress is one of the major natural issues resulting in stunted growth and loss of agricultural productivity. Cultivated kiwifruits are popular for their rich vitamin C content and unique flavor among consumers, while commonly sensitive to waterlogging stress. The wild kiwifruit plants are usually obliged to survive in harsh environments. Here, we carried out a transcriptome analysis by high-throughput RNA sequencing using the root tissues of Actinidia deliciosa (a wild resource with stress-tolerant phenotype) after waterlogging for 0 d, 3 d, and 7 d. Based on the RNA sequencing data, a high number of differentially expressed genes (DEGs) were identified in roots under waterlogging treatment, which were significantly enriched into four biological processes, including stress response, metabolic processes, molecular transport, and mitotic organization, by gene ontology (GO) simplify enrichment analysis. Among these DEGs, the hypoxia-related genes AdADH1 and AdADH2 were correlated well with the contents of acetaldehyde and ethanol, and three transcription factors Acc26216, Acc08443, and Acc16908 were highly correlated with both AdADH1/2 genes and contents of acetaldehyde and ethanol. In addition, we found that there might be an evident difference among the promoter sequences of ADH genes from A. deliciosa and A. chinensis. Taken together, our results provide additional information on the waterlogging response in wild kiwifruit plants.

Sweet cherry (Prunus avium L.) is widely planted in northern China due to its high economic value, and its cultivation has gradually spread south to warm regions. However, fruit rot, observed on the young fruits, poses a considerable threat to the development of sweet cherry. To determine the causal agent, morphological observation, molecular identification, and pathogenicity tests were performed on isolates obtained from diseased fruits. As a result, Sclerotinia sclerotiorum was identified as the pathogen. Pathogenicity tests on different sweet cherry cultivars indicated that ‘Summit’ was highly sensitive to S. sclerotiorum, whereas ‘Hongmi’ showed significant resistance. Besides sweet cherry, S. sclerotiorum could also infect other vegetable crops we tested, such as cowpea, soybean, tomato, and chili. Fungicide sensitivity and efficacy assays showed that both fludioxonil and pyraclostrobin can effectively inhibit the mycelial growth of S. sclerotiorum and decrease disease incidences on the young fruits of sweet cherry. Furthermore, genome sequencing resulted in a 37.8 Mb assembly of S. sclerotiorum strain ScSs1, showing abundant SNPs, InDels, and SVs with the genome of S. sclerotiorum reference strain 1980 UF-70. The above results provide an important basis for controlling the fruit rot of sweet cherry caused by S. sclerotiorum in China.

Lead (Pb) contamination in Moso bamboo forests poses a challenge in terms of sustainable development and raises concerns about the safety of bamboo shoots for consumption. However, the physiological impacts of Pb stress on Moso bamboo growth and the molecular mechanisms governing its adaptive responses remain poorly understood. This study comprehensively investigated the physiological and transcriptomic responses of Moso bamboo to Pb stress. The results showed that low concentrations (1–10 µM) of Pb stress had minimal adverse effects on biomass accumulation and the photochemical quantum yield of PSII in Moso bamboo. However, at a high Pb concentration (50 µM), the growth of roots was significantly inhibited, while Pb accumulation in the roots and shoots reached 15,611 mg·kg⁻¹ and 759 mg·kg⁻¹, respectively. The uptake of Pb was increased as the external Pb concentration increased, but the xylem loading of Pb reached saturation at 57.79 µM after six-hour exposure. Pb was mainly localized in the epidermis and pericycle cells in the roots, where the thickening of cell walls in these cells was found after Pb treatment. Transcriptomic profiling identified 1485 differentially expressed genes (DEGs), with significant alterations in genes associated with metal cation transporters and cell wall synthesis. These findings collectively indicate that Moso bamboo is a Pb-tolerant plant, characterized by a high accumulation capacity and efficient xylem loading. The tolerance mechanism likely involves the transcriptional regulation of genes related to heavy metal transport and cell wall biosynthesis.