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Loquat (Eriobotrya japonica Lindl.) is an evergreen fruit tree species of the Rosaceae, and its unique flowering time greatly hinders its production. To explore the artificial regulation of loquat flowering time, we removed the main inflorescence (by cutting it) to induce reflowering. For different loquat tree cultivars with different stages, the inflorescence was removed by cutting the main floral axis at two alternative positions: the upper or the lower position beneath the inflorescence, and it was found that the proportion of reflowering resulting from removing the upper position of the main floral axis of yellow-flesh loquat cultivars during the full-bloom stage was the highest. In addition, compared with those of the normal-growing panicles, the number of flower buds and branch axes of the reflowering panicles decreased significantly after cutting. Importantly, these newly produced inflorescences flowered 2–4 months later than normal-growing inflorescences did, effectively prolonging both the flowering and fruiting time. In addition, qRT-PCR results showed that EjFT1, EjFT2, EjAP1-1 and EjAP1-2 were highly expressed in the floral axis. These findings highlighted a new method for extending the production cycle of loquat and provided a reference for the flowering regulation of loquat and other economically important fruit tree species.

Sb2S3/perylene diimide derivatives composite micro-spheres composed of slight dendrites were synthesized by solvothermal reaction. Perylene diimide derivative with two carboxyl groups at amine position as morphology-controlling reagent is the key factor for determining the microscopic morphology of Sb2S3 in this system. Time-dependent experiments have been conducted to track the formation of Sb2S3 micro-spheres. Moreover, the composite material showed an excellent sensitivity of 29.8 μA mM−1 cm2 with a low detection limit of 50 pM, it also showed better stability and selectivity in hydrazine detection. This approach not only regulate the morphology and composition of Sb2S3 submicron materials effectively, but also provide new ideas for the manufacture of metal sulfide- perylenediimide amino acid derivative materials, which will be suitable for sensing, catalysis, and photovoltaic applications.

We studied the cross-compatibility among 91 inter-specific combinations and 21 inter-generic combinations in 7 Eriobotrya plants and 2 related genera (Raphiolepis indica Lindl. and Photinia serrulata Lindl.) using emasculation, bagging, and artificial pollination. Our results showed that 28 of the 91 inter-specific combinations set no fruit, which means nearly 30% of the combinations were incompatible. In the remaining 63 combinations, most showed partial cross-compatibility, and a few showed complete cross compatibility. Eriobotrya plants were incompatible with plants from their related genera (R. indica Lindl. and P. serrulata Lindl.). Backcrossing produced 5 compatible combinations, which could set fruits and produce F1 progeny but only after embryo rescue. Fruit setting ratios varied among various species used as male or female parents. E. prinoides Rehd. & Wils., common loquat (E. japonica) and Eriobotrya × daduheensis, used as female parents resulted in an average fruit-setting ratio of 36.2%–58.2%. E. deflexa Nakai and its two forms, and E. elliptica Lindl. as female parents resulted in 2.9%–16.3% average fruit-setting ratio; however, the fruit set ratio was higher (22.4%–43.1%) if they were used as male parents. Failure of E. deflexa f. koshunensis Nakai × E. prinoides Rehd. & Wils. hybrids to set fruit could be attributed to sporophytic incompatibility.

Perylene diimide and its various derivatives tend to form stable anion radicals, which can usually form a variety of aggregates with special properties. Herein, we reported synthesis and properties of the benzo[ghi]perylene trimide and its anion radical π-bonded dimer. The dimer exhibited high stable in solid status and in most organic solvents, but conversion of L-type π-bonded dimer to face to face type π-bonded dimer or π-stacked oligomer occurs in dimethyl formamide solution. The temperature and crystallization influenced the π-bonded length in the dimer and the partial memory can be reserved and probed in solution at room temperature.