Dew water is water droplets formed due to condensation of atmospheric water vapor on surfaces of temperature below its dew point temperature. Dew water can be seen as a nonconventional source of water and may be exploited in regions where weather conditions favor dew formation and inadequate supply and quality of water is a prevalent problem. There are two main types of dew condenser, the apparatus used to collect dew water, namely radiative (also called passive) and active condensers. Radiative passive collectors rely on exploiting the physical processes responsible for dew formation to collect dew water without any additional energy input. Previous studies indicate that a 1 m 2 radiative condenser yields between 0.3 and 0.6 L/day of dew water in arid and semi-arid regions. Active condensers have been designed as an alternative method of collection that produces higher yields by using additional energy inputs. Several designs of active condensers have been patented for which the yield can reach 20 L/day for portable devices, and up to 200,000 L/day for larger agricultural water devices. Active condensers are also known as atmospheric water generators, dehumidifiers, and air to water devices. Most of the active condensers are based on a regenerative desiccant that attracts and holds large volumes of water from the air or on a means of cooling the condensing surface below the dew point temperature (refrigeration circuit). The larger yields and wider range of environmental conditions in which dew can be collected make active condensers a promising option as an alternative or supplemental source of water in water scarce regions. The aim of this paper was to provide a comprehensive review of radiative and active condensers, including dew formation processes, methods of dew collection, and parameters that influence the dew collection. Subsequently, patents of active condensers were reviewed to ascertain how they can be integrated with different types of renewable energy and to assess the potential use of such integrated systems as a sustainable source of water in regions that suffer water scarcity and/or as a sustainable source of water for agriculture.

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Since plug seedling plays a key role in automatic transplanting, this work aimed to explore the effect biochar has on the root growth of plug seedlings. The physicochemical properties tests showed that the addition of biochar in the peats could increase the porosity, pH, and EC values of the substrate, and the substrates treated with 0%, 10%, 20%, and 30% biochar could meet the requirements of seedling raising. The water retention of the substrate was superior with the increase of biochar proportion, and the nitrogen release significantly decreased with the increase of the biochar proportion. Our results demonstrated that the substrate with 10% biochar-treated apparently promoted the growth of seedlings and root systems, even the length of the root-tip cells. However, the substrates with 40% and 50% biochar-treated obviously inhibited the growth of seedlings and root systems. It was noticed that the strength of substrate with appropriate biochar proportion was enhanced, as well. Under the interaction of strong root system and solid substrate, the compressive strength of the substrate with 20% and 10% biochar-treated was much better than others, especially that of 40% and 50% biochar-treated, which efficiently satisfied the requirements of automatic seedling picking. The biochar may have a good application prospect in seedling raising.

A Gram-stain-negative, aerobic, non-motile, salt- and alkali-tolerant, pear to oval shaped, rosette-forming, white coloured, bacterium, designated as strain JC646T, was isolated from a sediment sample collected from Chilika lagoon, India. Strain JC646T reproduced through budding, grew well at up to pH 9.0 and tolerated up to 7 % NaCl. Strain JC 646T utilized α-d-glucose, fumarate, lactose, sucrose, fructose, d-galactose, mannose, maltose and d-xylose as carbon sources. Peptone, l-isoleucine, l-serine, l-lysine, l-glutamic acid, l-aspartic acid, dl-threonine and l-glycine were used by the strain as nitrogen sources for growth. The respiratory quinone was MK6. Major fatty acids were C16 : 1 ω7c/C16 : 1 ω6c and C16 : 0. The polar lipids of strain JC646T comprised phosphatidyl-dimethylethanolamine, phosphatidylcholine, diphosphatidylglycerol, an unidentified amino lipid and two unidentified lipids. Strain JC646T had highest (97.3 %) 16S rRNA gene sequence identity to the only species of the genus Gimesia , Gimesia maris DSM 8797T. The genome of strain JC646T was 7.64 Mbp with a DNA G+C content of 53.2 mol%. For the resolution of the phylogenetic congruence of the novel strain, the phylogeny was also reconstructed with the sequences of 92 housekeeping genes. Based on phylogenetic analyses, digital DNA–DNA hybridization (19.0 %), genome average nucleotide identity (74.5 %) and average amino acid identity/percentageof conserved proteins (77 %) results, chemotaxonomic characteristics, and differential physiological properties, strain JC646T is recognized as representing a new species of the genus Gimesia , for which we propose the name Gimesia chilikensis sp. nov. The type strain is JC646T (=KCTC 72175T=NBRC 113881T).

Glutamine is a non-essential amino acid that acts as a principal source of nitrogen and nucleic acid biosynthesis in living organisms. In Saccharomyces cerevisiae, glutamine synthetase catalyzes the synthesis of glutamine. To determine the role of glutamine synthetase in the development and pathogenicity of plant fungal pathogens, we used S. cerevisiae Gln1 amino acid sequence to identify its orthologs in Magnaporthe oryzae and named them MoGln1, MoGln2, and MoGln3. Deletion of MoGLN1 and MoGLN3 showed that they are not involved in the development and pathogenesis of M. oryzae. Conversely, ∆Mogln2 was reduced in vegetative growth, experienced attenuated growth on Minimal Medium (MM), and exhibited hyphal autolysis on oatmeal and straw decoction and corn media. Exogenous l-glutamine rescued the growth of ∆Mogln2 on MM. The ∆Mogln2 mutant failed to produce spores and was nonpathogenic on barley leaves, as it was unable to form an appressorium-like structure from its hyphal tips. Furthermore, deletion of MoGLN2 altered the fungal cell wall integrity, with the ∆Mogln2 mutant being hypersensitive to H2O2. MoGln1, MoGln2, and MoGln3 are located in the cytoplasm. Taken together, our results shows that MoGLN2 is important for vegetative growth, conidiation, appressorium formation, maintenance of cell wall integrity, oxidative stress tolerance and pathogenesis of M. oryzae.