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Abstract In this work, we present the results of the ortho-positronium (o-Ps) annihilation lifetimes and nitrogen adsorption measurements for different porous materials and an approach for describing the annihilation of o-Ps in a pore, which results in a surface-volume formula (SVF) for calculating the pore-related o-Ps lifetime. This proposed formula gives the relationship between the o-Ps annihilation rate and the effective pore radius, bulk composition, and pore structure, including pore geometry and topology. The pore-related o-Ps lifetimes of different materials calculated by the SVF are consistent with experimental results for both micro- and mesopores (and macropores) with different geometries and topologies. The SVF is convenient for calculations of pore dimensions for many cases of metal organic frameworks and zeolites. This approach enables us to fully explain the temperature dependence of the o-Ps annihilation lifetime over a wide temperature range, 20–700 K.

Abstract The lipid storage droplet-2 (LSD-2) protein of Drosophila is a homolog of mammalian perilipin 2, which is essential for promoting lipid accumulation and lipid droplet formation. The function of LSD-2 as a regulator of lipolysis has also been demonstrated. However, other LSD-2 functions remain unclear. To investigate the role of LSD-2, we performed tissue-specific depletion in the salivary glands of Drosophila using a combination of the Gal4-upstream activating sequence system and RNA interference. LSD-2 depletion inhibited the entry of salivary gland cells into the endoreplication cycle and delayed this process by enhancing CycE expression, disrupting the development of this organ. The deficiency of LSD-2 expression enhanced reactive oxygen species production in the salivary gland and promoted JNK-dependent apoptosis by suppressing dMyc expression. This phenomenon did not result from lipolysis. Therefore, LSD-2 is vital for endoreplication cell cycle and cell death programs.