the damage caused by cold injury. The results also showed that V. fordii seedlings are more resistant to low temperatures than V. montana seedlings.

Background The oil-tea tree (Camellia oleifera Abel.) is a woody tree species that produces edible oil in the seed. C. oleifera oil has high nutritional value and is also an important raw material for medicine and cosmetics. In China, due to the uncertainty on maturity period and oil synthesis mechanism of many C. oleifera cultivars, growers may harvest fruits prematurely, which could not maximize fruit and oil yields. In this study, our objective was to explore the mechanism and differences of oil synthesis between two Camellia oleifera cultivars for a precise definition of the fruit ripening period and the selection of appropriate cultivars. Results The results showed that ‘Huashuo’ had smaller fruits and seeds, lower dry seed weight and lower expression levels of fatty acid biosynthesis genes in July. We could not detect the presence of oil and oil bodies in ‘Huashuo’ seeds until August, and oil and oil bodies were detected in ‘Huajin’ seeds in July. Moreover, ‘Huashuo’ seeds were not completely blackened in October with up to 60.38% of water and approximately 37.98% of oil in seed kernels whose oil content was much lower than normal mature seed kernels. The oil bodies in seed endosperm cells of ‘Huajin’ were always higher than those of ‘Huashuo’ from July to October. Conclusion Our results confirmed that C. oleifera ‘Huashuo’ fruits matured at a lower rate compared to ‘Huajin’ fruits and that ‘Huajin’ seeds entered the oil synthesis period earlier than ‘Huashuo’ seeds. Moreover, ‘Huashuo’ fruits did not mature during the Frost’s Descent period (October 23–24 each year).

‘Huaxin’ is a new high-yielding timber cultivar of Camellia oleifera of high economic value, and has been widely cultivated in the red soil hilly region of Hunan Province of the People´s Republic of China in recent years. However, its quality and production are severely affected by low temperatures during flowering. To find genes related to cold tolerance and further explore new candidategenes for chilling-tolerance, Illumina NGS (Next Generation Sequencing) technology was used to perform transcriptomic analyses of C. oleifera ‘Huaxin’ leaves under long-term cold stress. Nine cDNA libraries were sequenced, and 58.31 Gb high-quality clean reads were obtained with an average of 5.92 Gb reads for each sample. A total of 191,150 transcripts were obtained after assembly. Among them, 100,703 unigenes were generated, and 44,610 unigenes were annotated. In total, 1564 differentially expressed genes (DEGs) were identified both in the A_B and A_C gene sets. In the current study, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were performed, andrevealed a group of cold-responsive genes related to hormone regulation, photosynthesis, membrane systems, and osmoregulation; these genes encoded many key proteins in plant biological processes, such as serine/threonine-protein kinase (STPK), transcription factors (TFs), fatty acid desaturase (FAD), lipid-transfer proteins (LTPs), soluble sugars synthetases, and flavonoid biosynthetic enzymes. Some physiological indicators of C. oleifera ‘Huaxin’ were determined under three temperature conditions, and the results were consistent with the molecular sequencing. In addition, the expression levels of 12 DEGs were verified using quantitative real-time polymerase chain reaction (qRT-PCR). In summary, the results of DEGs analysis together with qRT-PCR tests contribute to the understanding of cold tolerance and further exploring new candidate genes for chilling-tolerance in molecular breeding programs of C. oleifera ‘Huaxin’.

As a result of its high photosynthetic efficiency, the tung tree (Vernicia fordii) is a fast-growing heliophile, yielding fruit within 3 years. In addition, tung oil extracted from the fruit seeds is an environmentally friendly paint used widely in China. However, mutual shading inside a tung tree canopy leads to a low yield of fruit because of weak or dead lower branches. In this project, a pot experiment was conducted to understand the growth, physiological, anatomical structure, and biochemical responses of tung trees under various shading levels. Tung tree seedlings were subjected to different light intensities—100% sunlight (no cover), L100; 75% sunlight (25% shading), L75; 50% sunlight (50% shading), L50; and 20% sunlight (80% shading), L20—from June to August. Results indicate that the L75 treatment reduced significantly the net photosynthetic rate (Pn), stomatal conductance (gS), transpiration rate (E), total aboveground and root dry weight (DW), maximum net photosynthetic rate (Amax), and maximum rate of electron transport at saturating irradiance (Jmax) compared with the control, although plant height and leaf area (LA) were not reduced. Lower light intensities (L50 and L20) and longer duration of treatment led to greater reduction in growth, leaf thickness, and photosynthetic potential (Amax and Jmax). Chlorophyll a (Chl a), chlorophyll b (Chl b), and total chlorophyll content were increased in the L50 and L20 treatments compared with L100 and L75. There was no significant reduction in the enzyme activities of ribulose-1,5-bisphosphate carboxylase (Rubisco) and phosphoenolpyruvate (PEPC) of the seedlings using the L75 treatment; however, lower light intensities (L50 and L20) and longer duration of shade treatment resulted in a significant reduction in enzyme activity. In summary, the results suggest that tung trees have greater photosynthetic activity under high light intensity. Shading, even at 20%, especially for the longer term, reduced photosynthetic efficiency and growth. To prevent growth reduction, tung trees should be grown under full sun with a daily light integral (DLI) of ≈46 mol·m‒2·d‒1, and mutual shading should be avoided by proper spacing and pruning.