Floral longevity (FL) is an important floral functional trait which is critical for flowering plants. FL shows great diversity among angiosperms; however, there is limited information on the mechanisms that influence differences in floral longevity, especially the relationship between petal anatomical traits and floral longevity. We aimed to examine (1) the relationships between petal anatomical traits and FL in tree peony cultivars and (2) the petal anatomical characteristics of longer FL cultivars. Eleven traits of six tree peony cultivars with different FL were investigated, including six water conservation traits (petal thickness, cuticle thickness, number of cell layers, mesophyll thickness, adaxial epidermis thickness and abaxial epidermis thickness), three water supply traits (vein density, number of xlylem vessels and xylem vessel diameter), petal fresh mass and petal dry mass across cultivars. There are significant differences in traits related to water conservation and water supply ability of tree peonies with different FL. Tree peony cultivars with long FL were characterized by the thicker Mesophyll, cuticles, adaxial and abaxial epidermis of the petals. There was a positive correlation between FL and vessel number and vessel diameter. These results suggest that the ability to retain water in flowers is associated with floral longevity. Petal traits related to water conservation and supply, including vein densities, mesophyll thickness, and epidermis thickness, are beneficial for prolonging the flower longevity in tree peonies.

This research reports for the first time the epidermal characteristics of 10 wild tree peonies belonging to the sect. Moutan group. The leaf micromorphology of 10 wild tree peonies—P. qiui, P. decomposita, P. jishanensis, P. ostii, P. delavayi, P. lutea, P. potanini, P. rockii, P. ludlowii and P. cathayana—were investigated by light and scanning electron microscopy. The characteristics of the leaf epidermis were found to be constant at the species level, but variable among species. Patterns of anticlinal walls were slightly wavy to wavy, very wavy, and straight to curved. All studied tree peonies presented stomata only on the abaxial surfaces of the leaves. The stomatal apparatus was elliptical or rectangular. Stomatal density was highest on the abaxial surface in P. qiui (300.25 per mm²), and lowest in P. jishanensiss (198.41 per mm²). Stomatal Index was highest on the adaxial surface of P. potanini (27.30%), and lowest in P. ludlowii (18.35%). Trichomes were observed in four studied peonies, which appeared only on the abaxial surface of the leaves, and three basic types of trichomes were identified. The long conical trichomes were distinctive of P. jishanensis, and the flat-shaped trichomes were characteristic of P. qiui, P. rockii and P. cathayana, and commonly occurred in the intervenous region and leaf veins. Stomatal shape, stomatal density, anticlinal wall patterns and trichomes may be of great value and significance for the classification of wild tree peonies. The principal component analysis showed that the component 1, component 2 and component 3 were the most components and nearly 79% of the observed variation. The key to the identification of wild tree peonies based on trichomes and stomata diversity was provided.

The relationship between metabolite changes and biological endpoints in response to cadmium (Cd) stress remains unclear. Fountain grass has good Cd enrichment and tolerance abilities and is widely used in agriculture and landscaping. We analyzed the metabolic responses by detecting the metabolites through UPLC-MS and examined the relationships between metabolite changes and the characteristics of morphology and physiology to different Cd stress in fountain grass. Our results showed that under Cd stress, 102 differential metabolites in roots and 48 differential metabolites in leaves were detected, with 20 shared metabolites. Under Cd stress, most of the carbohydrates in leaves and roots decreased, which contributed to the lowered leaf/root length and fresh weight. In comparison, most of the differential amino acids and lipids decreased in the leaves but increased in the roots. Almost all the differential amino acids in the roots were negatively correlated with root length and root fresh weight, while they were positively correlated with malondialdehyde content. However, most of the differential amino acids in the leaves were positively correlated with leaf length and leaf fresh weight but negatively correlated with malondialdehyde content. Metabolic pathway analysis showed that Cd significantly affects seven and eight metabolic pathways in the leaves and roots, respectively, with only purine metabolism co-existing in the roots and leaves. Our study is the first statement on metabolic responses to Cd stress and the relationships between differential metabolites and biological endpoints in fountain grass. The coordination between various metabolic pathways in fountain grass enables plants to adapt to Cd stress. This study provides a comprehensive framework by explaining the metabolic plasticity and Cd tolerance mechanisms of plants.

Tree peonies (Paeonia suffruticosa Andr. and hybrids) are well-known ornamental and medicinal plants cultivated in temperate and subtropical regions around the world. From June to September 2021, severe leaf spot disease was observed on 3 tree peony cultivars (‘Luoyanghong’, ‘Moyushenghui’, ‘Roufurong’) in Xinxiang (35º29´N, 113º95´E) and Luoyang (34º64´N, 112º49´E), Henan Province, China. Leaf spot incidence was as high as 28% (‘Luoyanghong’), 45% (‘Moyushenghui’) and 67% (‘Roufurong’), respectively. Symptoms appeared initially as small purple spots less than 1 mm in diameter in the middle and upper parts of the leaves, and then evolved to coalescent lesions, causing brown scorch ultimately. From each cultivar, 5 diseased leaves were collected. Leaflet tissues (3-4 mm2) cut from spot margins were surface sterilized in 75% alcohol for 45 s, washed 5 times with sterile distilled water, and then cultivated on potato dextrose agar (PDA) medium at 28 °C in the dark. Eleven isolates were obtained, and colonies grown from single conidia on PDA were 80-85 mm in diameter after 10 d, with scattered small, dark-based spikes on the surface of the colonies. The aerial mycelium was cottony, dense, and dark gray near the center on the reverse side. Conidia were cylindrical to clavate, with rounded apex and rounded base, and the conidia contents were granular, 8.44-14.06×3.60-4.31 μm (mean=11.28×3.69 μm, n=40). Appressoria were mostly subglobose or with a few broad lobes, pale to medium brown, 3.36-6.72×3.35-5.60 μm (mean=5.02×4.55 μm, n=20). Based on the culture representation and conidial morphology, the isolates were characterized as Colletotrichum gloeosporioides species complex (Weir et al. 2012; Fu et al. 2019). To further identity the species, the actin (ACT), calmodulin (CAL), chitin synthase (CHS-1), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and the ribosomal internal transcribed spacers (ITS) loci of isolates PSW0002, PSW0008 and PSW0009 were amplified using ACT-512F/ACT-783R, CL1C/CL2C, CHS-79F/CHS-345R, GDF/GDR, and ITS1/ITS4, primers (Weir et al. 2012; Schena et al; 2014; Kim et al. 2021; Li et al. 2021). Fifteen sequences were deposited in GenBank (ACT for OP225605, OP225606, and OP225607, CAL for OP225608, OP225609 and OP225610, CHS for OP225611, OP225612 and OP225613, GAPDH for ON321897, OP225614, and OP225615, and ITS for ON323473, OP214349 and OP214350 ), which showed 100% sequence similarity to Colletotrichum aenigma (JX009443 and JX009519 for ACT, JX009683 and JX009684 for CAL, JX009774 and JX009903 for CHS-1, JX010244 and JX009913 for GAPDH, JX010243 and JX010148 for ITS). Three isolates clustered with C. aenigma (ex-holotype culture ICMP 18608) in the multi-locus phylogenetic tree with a bootstrap value of 100%. To achieve Koch's postulates, pathogenicity was tested on 5-year-old healthy potted plants (‘Luoyanghong’). Thirty leaves were inoculated with 10 µL conidial suspension (isolate PSW0002, 1×106 conidia/mL) and the controls were inoculated with sterile water. Plants were placed in a greenhouse at 28°C under conditions with 12 h photoperiod and 90% relative humidity. After 5 to 10 days, distinct spots were observed on the inoculated leaves, while the control leaves showed no symptoms. C. aenigma was reisolated from all inoculated leaves, but not from the control. C. aenigma has been reported to cause anthracnose on Pyrus pyrifolia (Weir et al. 2012), Camellia sasanqua (Chen et al. 2019), Juglans regia (Wang et al. 2020), Paeonia ostii (Ren et al. 2020), and Capsicum annuum (Sharma et al. 2022). A previous study reported C. gloeosporioides as a pathogen of anthracnose in tree peonies in China (Xuan et al. 2017), the typical symptoms were big necrotic lesions (5-10 mm diam) on leaves，which were significantly different from those caused by C. aenigma. To our knowledge, this is the first report of C. aenigma causing anthracnose in tree peonies in China. This finding may help to take effective control of anthracnose in tree peonies.

Peonies are globally renowned ornamental plants, and distant hybridization is a key method for breeding new varieties, though it often faces cross-incompatibility challenges. The metabolic mechanisms underlying the crossing barrier between tree peony (Paeonia sect. Moutan) and herbaceous peony (P. lactiflora) remain unclear. To identify key metabolites involved in cross-incompatibility, we performed a cross between P. ostii ‘Fengdanbai’ (female parent) and P. lactiflora ‘Red Sara’ (male parent) and analyzed metabolites in the stigma 12 h after pollination using UPLC-MS. We identified 1242 differential metabolites, with 433 up-regulated and 809 down-regulated, including sugars, nucleotides, amino acids, lipids, organic acids, benzenoids, flavonoids, and alkaloids. Most differential metabolites were down-regulated in hybrid stigmas, potentially affecting pollen germination and pollen tube growth. Cross-pollinated stigma exhibited lower levels of high-energy nutrients (such as amino acids, nucleotides, and tricarboxylic acid cycle metabolites) compared to self-pollinated stigma, which suggests that energy deficiency is a contributing factor to the crossing barrier. Additionally, cross-pollination significantly impacted KEGG pathways such as nucleotide metabolism, purine metabolism, and vitamin B6 metabolism, with most metabolites in these pathways being down-regulated. These findings provide new insights into the metabolic basis of cross-incompatibility between tree and herbaceous peonies, offering a foundation for overcoming hybridization barriers in peony breeding.