Volume and mass of coarse woody debris (> 20 cm diameter) in an old-growth forest on the Cumberland Plateau in southeastern Kentucky averaged 66.3 m3/ha and 21.8 Mg/ha, respectively. Coarse woody debris was patchily distributed among 80 sample plots (0.04 ha each), with 10 plots containing 39% of the total mass. Coarse woody debris mass was inversely, although not strongly, related to plot basal area. While 23 species contributed to the accumulation of coarse woody debris, five accounted for 72% of the total mass. These included Quercusprinus L. (25% of the total), Fagusgrandifolia L. (16%), Quercusalba L. (12%), Castaneadentata (Marsh.) Borkh. (11%), and Quercusvelutina Lam. (9%). The few studies of coarse woody debris in old-growth deciduous forests of North America suggest a regional pattern of accumulation correlated with temperature. In warmer regions, old-growth deciduous forests accumulate a mass in the range of 22–32 Mg/ha, while in cooler ecosystems, coarse woody debris ranges from 34 to 49 Mg/ha.

Phytochrome-interacting factors (PIFs) regulate an array of developmental responses ranging from seed germination to vegetational architecture in Arabidopsis. However, information regarding the functions of the PIF family in monocots has not been widely reported. Here, we investigate the roles of OsPIL15, a member of the rice (Oryza sativa L. cv. Nipponbare) PIF family, in regulating seedling growth. OsPIL15 encodes a basic helix-loop-helix factor localized in the nucleus. OsPIL15-OX seedlings exhibit an exaggerated shorter aboveground part and undeveloped root system relative to wild-type seedlings, suggesting that OsPIL15 represses seedling growth in the dark. Microarray analysis combined with gene ontology analysis revealed that OsPIL15 represses a set of genes involved in auxin pathways and cell wall organization or biogenesis. Given the important roles of the auxin pathway and cell wall properties in controlling plant growth, we speculate that OsPIL15 represses seedling growth likely by regulating the auxin pathway and suppressing cell wall organization in etiolated rice seedlings. Additionally, exposure to red light or far-red light relieved growth retardation and promoted seedling elongation in the OsPIL15-OX lines, despite higher levels of OsPIL15 transcripts under red light and far-red light than in the dark. These results suggest that light regulation of OsPIL15 expression is probably involved in photomorphogenesis in rice.

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Long non‐coding RNA (lncRNA) plays important roles in tumour progression. Accumulating studies demonstrated that lncRNA colon cancer‐associated transcript 2 (CCAT2) acted as an oncogene in many tumours. However, the role of CCAT2 in the development of osteosarcoma has not been elucidated. In our study, we indicated that CCAT2 expression was up‐regulated in osteosarcoma tissues and cell lines (SOSP‐9607, MG‐63, U2OS and SAOS‐2). In addition, osteosarcoma cases with higher CCAT2 expression had a poorer disease‐free survival and shorter the overall survival time compared to those with lower expression. Overexpression of CCAT2 promoted osteosarcoma cell proliferation, invasion and cell cycle. Furthermore, ectopic expression of CCAT2 increased the expression of mesenchymal markers N‐cadherin, vimentin and snail and reduced the expression of N‐cadherin marker E‐cadherin. CCAT2 overexpression promoted the LATS2 and c‐Myc expression in osteosarcoma cell. These data indicated that CCAT2 served as an oncogene in osteosarcoma and promoted osteosarcoma cell proliferation, cell cycle and invasion.