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Chrysanthemum (Chrysanthemum ×morifolium) is a common ornamental crop with a qualitative short-day flowering response. Extending a short day with moderate blue [B (400–500 nm)] light inhibits flowering in greenhouse conditions with sunlight but does not indoors (without sunlight) under B + red [R (600–700 nm)] light or white light. We postulated that the contrasting responses to B light as a day extension depended on far-red [FR (700–800 nm)] light during the day, which is plentiful under sunlight but lacking indoors under B+R or white light-emitting diodes. To study this response in three chrysanthemum cultivars, we delivered indoor lighting treatments at two locations with an 11-hour main photoperiod of B, green [G (500–600 nm)], R, and FR light, where subscript values indicate the photon flux density (in µmol·m−2·s−1) of each waveband: B60R120, B60G60R60, and B60R60FR60. After each short main photoperiod, plants received 0 or 4 hours of day-extension lighting of 60 µmol·m−2·s−1 of B light (B60). Under all treatments except B60R60FR60 with day-extension B60, it took ‘Chelsey Pink’, ‘Gigi Gold’, and ‘Gigi Yellow’ 13 to 17 days to reach the first visible inflorescence and 42 to 51 days to the first open flower. In contrast, plants grown under B60R60FR60 with day-extension B60 took 41 to 67 days to reach the first visible inflorescence with few plants developing open flowers. Plants were tallest at the first open flower and after 9 weeks of treatments when grown under B60R60FR60 with day-extension B60. These results indicate that the inclusion of FR light, but not G light, in the main photoperiod is necessary for day-extension B light to inhibit flowering in chrysanthemum. On the basis of these results and those of other studies, we postulate that the spectral dependence of flowering in chrysanthemum depends on whether and how the phytochrome photoequilibrium changes during the day. In particular, a sufficiently high daytime phytochrome photoequilibrium (e.g., under B+R and B+G+R light) could establish a predominant mode of floral signaling that prevents perception of subsequent B light as a long day.
There is demand for early-flowering cannabis (Cannabis sativa) cultivars to hasten harvest and avoid late-season detrimental weather conditions. A field study and greenhouse studies were conducted to evaluate the effect of gene dosage at the autoflowering locus on flowering timing for diploid and triploid hybrids between autoflowering and photoperiod-sensitive parents. Autoflowering × photoperiod-sensitive hybrids were all photoperiod sensitive, but their critical photoperiods were longer than for homozygous photoperiod-sensitive plants, which resulted in earlier flowering. For triploid genotypes, decreasing dosage of the photoperiod-sensitive allele (A), from AAA to AAa to Aaa, reduced the time to flowering. Flowering timing for the diploid genotype Aa was intermediate between Aaa and AAa. These results provide evidence of incomplete dominance of the A allele at the autoflowering locus. Plants of genotype Aaa flowered 32 to 40 days earlier in the field than genotypes of AA, 15 days earlier than genotype Aa, and were ready for harvest by the second week of August in Connecticut. Plants of Aaa were as tall as other diploid and triploid photoperiod-sensitive genotypes studied, which suggests that they have similar yield potential. The use of tetraploid autoflowering (aaaa) maternal plants in combination with diploid photoperiod-sensitive (AA) pollen parents to produce Aaa genotype seed is a reliable approach for developing early-flowering cultivars of cannabis for flower production purposes.
In response to challenges caused by climate change, apple (Malus ×domestica) breeding programs must quickly develop more resilient cultivars. One strategy is to breed for various bloom times. Members of the genus Malus, including domesticated apple, wild species, and hybrids, exhibit striking variations in the bloom date. Although bloom time is strongly influenced by chilling requirements, other aspects of floral development in Malus and their contributions to bloom time are less known. The purpose of this study was to investigate potential connections between predormancy flower development and final bloom time in Malus species. We performed a phenological analysis of flower development in wild and domesticated apple with extreme differences in bloom time over the course of one developmental season. We tracked histological changes in the floral apex of representatives of three early-blooming Malus genotypes (M. ×domestica ‘Anna’ PI 280400, M. orthocarpa PI 589392, M. sylvestris PI 633824) and three late-blooming genotypes (M. angustifolia PI 589763, M. angustifolia PI 613880, M. ×domestica ‘Koningszuur’ PI 188517). Our study documented their floral meristem progression and organ development and expanded on current staging systems for apple flower development to describe the changes observed. The developmental trajectories of each genotype did not group according to bloom category, and we observed variations in the floral development stage at the time of dormancy onset.
This study explored the effects of Ustilago esculenta inoculation on physiological responses (activities of defense and antioxidant enzymes) and chitinase gene expression in male Zizania latifolia “jiaobai” (without U. esculenta infection, with no galls, but normal flowering). Male jiaobai seedlings were injected at the five-leaf stage with U. esculenta suspension, and the impact on transcription of several genes encoding enzymes was examined. Compared with controls, expression of most enzymes was significantly different at 3 or 12 hours postinjection, and most ZlChi genes were involved in the response to U. esculenta inoculation. Fluorescence quantitative polymerase chain reaction results showed that U. esculenta was present in the roots of male jiaobai inoculated with U. esculenta at the shoot tips. Paraffin sections revealed many fungal hyphae in the roots at 15 d after inoculation, but few in controls. The results provide a basis for further study of the responses of male Z. latifolia to U. esculenta infection.
As one of the most important fruit tree crops, apple (Malus ×domestica), is faced with the serious impact of soil salinization. However, the underlying genetic and regulatory network remains elusive. Here, we adopted time-course RNA sequencing to decipher the genetic basis and regulatory module of apple in response to salt stress. Among a series of intense changes in genes at each time point, the critical genes in the mitogen-activated protein kinase signaling pathway were highly consistent with the duration of the stress treatment. Moreover, Salt Overly Sensitive 1 (SOS1) genes were identified and predicted to play important roles in the response process. We constructed coexpression modules and explored modules significantly associated with stress. SOS genes were identified in the hub genes, suggesting a critical role. Interestingly, transcription factors were also identified and predicted to cointeract with SOS genes in the hub genes of the coexpression module [e.g., HB7 (MD01G1226600), WRKY33 (MD12G1181000), and ERF106 (MD07G1248700)]. Collectively, our exploration and findings provide a reference and data resource for the study of genetic and salt regulatory networks in apple.
Agrobacterium rhizogenes transformation is a more rapid method of obtaining transgenic and edited rubber dandelion (Taraxacum kok-saghyz) plants than Agrobacterium tumefaciens. The hairy root rol genes are present alongside transgenes after transformation, and they change the morphology of rubber dandelion significantly. Although these rol genes are useful visual markers indicating successful transformation of rubber dandelion, they modify the phenotype induced by the target transgenes and are ultimately detrimental to agronomic traits. Fortunately, the rol genes can be removed by conventional plant breeding because they segregate in progeny separately from the targeted transgenes. However, it is preferable to have preliminary identification of promising effects induced by transgenes or gene edits before rol gene removal so that only the best plants are used for breeding. Therefore, the goal of this research was to characterize rol– and rol+ plant morphology so that, in the future, rol+ transgene+ plants can be easily distinguished from rol+ transgene– plants. This requires that rol gene–induced morphological changes and simply assayed physiological traits are first characterized thoroughly so that transgene changes may be observed. Taproot formation is reduced or eliminated in rubber dandelion by rol genes, and rol-induced hairy roots are identifiable easily because they grow shallowly in potting soil, so only partial unearthing is needed. Both leaf and flower numbers are increased by rol genes, but leaves and flowers are smaller than in rubber dandelion wild type with longer stalks. The rosette doming phenotype caused by the induction of a large number of leaf primordia is obvious in rooted plants as young as 1 month old. Photosynthetic rates are reduced significantly in rol+ plants, although growth is not. An accurate description of the morphology of rubber dandelion after A. rhizogenes transformation may allow for initial selection of promising transformed plants before confirmation with polymerase chain reaction, by phenotypic comparison of plants expressing transgenes and the rol gene, with those only expressing the rol gene.
Soil salinization is an environmental problem globally. Bermudagrass (Cynodon dactylon) has long been used for soil restoration in saline-alkali land. Urbanization and the compound planting pattern combining trees, bushes, and grasses induced shading are becoming one of the most significant environmental constraints on the management of bermudagrass, which directly affects photosynthetic characteristics. Salinity and shade have become the most important environmental constraints on lawn development and implementation. Previous studies have shown that the plant physiological response under combined stress was different from that under single stress. The purpose of this research was to investigate the effects of salinity stress, shade stress, and the combined stress on bermudagrass. Shade nets were used to simulate shade stress to 85% shade. The NaCl concentration gradient for salinity stress was 1.0% for 7 days, 1.5% for 7 days, and 2.0% for 13 days, respectively. The combined stress combines the two approaches mentioned previously. The results showed that the salinity stress significantly inhibited the plant height, leaf relative water content, chlorophyll content, the chlorophyll a fluorescence induction (OJIP) curve and other photosynthetic parameters of bermudagrass while increasing electrolyte leakage when compared with control. Shade stress significantly enhanced the plant height, chlorophyll content, electrolyte leakage, the OJIP curve, and other photosynthetic parameters. Under the combined stress, the plant height and relative water content did not change significantly, but the photosynthetic parameters such as chlorophyll content and the OJIP curve increased. Furthermore, under the combined stress, the photosynthesis-related genes were regulated. Salinity stress inhibited the photosynthetic ability of bermudagrass more than shade stress, while the combined stress exhibited a considerably better photosynthetic ability. These findings provide information for the usage of bermudagrass in salinized shade conditions.