These findings suggested that morin is a promising candidate for the development of anti-virulence therapeutic agents for the treatment of Staph. aureus infections.

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To study the phototactic responses of white‐backed planthopper, Sogatella furcifera (Horváth) and brown planthopper, Nilaparvata lugens (Stål) to different wavelengths, four colours of light traps (blue, green, yellow and red light‐emitting diodes) were placed in the same rice field along with a traditional black light trap. This study revealed that S. furcifera and N. lugens are more attracted to blue and green lights than that to yellow and red lights. During the 24 nights, compared with the black light trap, the blue LED trap could catch more rice planthoppers at 17 nights. Furthermore, catches of other species (moths and beetles) were substantially reduced in blue LED light traps. Multiple regression models were developed to assess the effect of weather factors on light trap catches of rice planthoppers. Rainfall and mean air temperature at a night mainly affected light trap catches of S. furcifera. Higher rainfall and lower temperature increased light trap catches of S. furcifera. However, wind speed was the main factor affecting the catches of N. lugens, and the lower incidence of catches was found in the night when wind speed exceeded 3.08 m/s. S. furcifera may be flying against wind at light wind nights by 0.3–1.5 m/s, whereas N. lugens may be flying down at strong wind nights by 1.5–3.08 m/s. Relative humidity did not significantly influence on trap catches. Consequently, light wavelengths, precipitation, average temperature and wind should be considered when monitoring rice planthoppers by light traps. Therefore, the blue LED light traps are worth using for monitoring planthoppers.

Stimulated emission depletion (STED) microscopy is a useful tool in investigation for super-resolution realm. By silencing the peripheral fluorophores of the excited spot, leaving only the very centre zone vigorous for fluorescence, the effective point spread function (PSF) could be immensely squeezed and subcellular structures, such as organelles, become discernable. Nevertheless, because of the low cross-section of stimulated emission and the short fluorescence lifetime, the depletion power density has to be extremely higher than the excitation power density and molecules are exposed in high risk of photobleaching. The existence of photobleaching greatly limits the research of STED in achieving higher resolution and more delicate imaging quality, as well as long-term and dynamic observation. Since the first experimental implementation of STED microscopy, researchers have lift out variety of methods and techniques to alleviate the problem. This paper would present some researches via conventional methods which have been explored and utilised relatively thoroughly, such as fast scanning, time-gating, two-photon excitation (TPE), triplet relaxation (T-Rex) and background suppression. Alternatively, several up-to-date techniques, especially adaptive illumination, would also be unveiled for discussion in this paper. The contrast and discussion of these modalities would play an important role in ameliorating the research of STED microscopy.