The Canadian Seasonal to Interannual Prediction System (CanSIPS) became operational at Environment Canada's Canadian Meteorological Centre (CMC) in December 2011, replacing CMC's previous two-tier system. CanSIPS is a two-model forecasting system that combines ensemble forecasts from the Canadian Centre for Climate Modeling and Analysis (CCCma) Coupled Climate Model, versions 3 and 4 (CanCM3 and CanCM4, respectively). Mean climate as well as climate trends and variability in these models are evaluated in freely running historical simulations. Initial conditions for CanSIPS forecasts are obtained from an ensemble of coupled assimilation runs. These runs assimilate gridded atmospheric analyses by means of a procedure that resembles the incremental analysis update technique, but introduces only a fraction of the analysis increment in order that differences between ensemble members reflect the magnitude of observational uncertainties. The land surface is initialized through its response to the assimilative meteorology, whereas sea ice concentration and sea surface temperature are relaxed toward gridded observational values. The subsurface ocean is initialized through surface forcing provided by the assimilation run, together with an offline variational assimilation of gridded observational temperatures followed by an adjustment of the salinity field to preserve static stability. The performance of CanSIPS historical forecasts initialized every month over the period 1981-2010 is documented in a companion paper. The CanCM4 model and the initialization procedures developed for CanSIPS have been employed as well for decadal forecasts, including those contributing to phase 5 of the Coupled Model Intercomparison Project.

We have used cationic oligopeptide polyarginine12mer (POA) to deliver double-stranded RNA (dsRNA), prepared in vitro, to tobacco (Nicotiana tabacum) suspension cells. POA interacts electrostatically with dsRNA to form a complex. When dsRNA for the GUS or NPTII gene was delivered into cells carrying the same genes, the corresponding mRNA was degraded. Using RNase protection assay we were able to detect 21-bp small interfering RNA in dsRNA/POAtreated cells. These results demonstrate that POA can be used to deliver dsRNA to induce post-transcriptional gene silencing in plant cells.

Rutin is an economically valuable flavone compound with anticancer activity, dietary effects, and anti-aging activity. In this study, callus and adventitious roots were induced from three Morus (mulberry) species.Among the three mulberry species tested for rutin production, roots of the Sugye (M. alba L.) had the highest levels (242.2 lg/g fresh tissue) of rutin. In addition, the mature leaves of this type of tree promoted higher levels of rutin compared to those of young leaves or those undergoing senescence. Adding auxins such as indole-3-acetic acid (IAA), 2,4-dichlorophenoxyacetic acid (2,4-D) and naphthalene-1-acetic acid (NAA) not only enhanced the development of callus and adventitious roots but also increased the protein and rutin contents. In contrast, adding cytokinins such as 6-benzyladenine (BA) and kinetin (KN) retarded callus and adventitious root development as well as the protein and rutin contents. Callus in suspension culture in the presence of IAA produced more rutin than that in the absence of IAA. However, rutin secretion into a medium was greater in the absence of IAA. Different ammonium/nitrate (AM/NI) ratios in a root suspension culture also greatly affected rutin production and its secretion into a liquid medium. As a result, the highest level of rutin was produced when adventitious roots were grown in a 34/66 AM/NI full-strength standard MS medium containing 5 mg/l IAA.

To effectively utilize the anisotropic characteristics of hexagonal boron nitride (h-BN), we have developed magnetic h-BN hybrid platelets decorated with iron oxide (Fe 3 O 4 ) nanoparticles, which are used as magnetic carriers for tailoring the anisotropy of h-BN. The as-synthesized Fe 3 O 4 -coated h-BN powders can easily move under a relatively low magnetic field. With the aid of iron oxide nanoparticles, h-BN platelets randomly dispersed in an epoxy matrix are successfully reoriented in a direction vertical to the film plane. Moreover, by utilizing the anisotropic characteristics of h-BN platelets, Fe 3 O 4 -coated h-BN/ epoxy composites exhibit exceptional performance in terms of in-plane thermal conductivity. This result is attributed to an improvement in the heat-transport pathways in composite films due to the anisotropic ordering of thermally conductive h-BN sheets. The Fe 3 O 4 -decorated h-BN platelets will be promising candidates for significantly improving the performances of advanced electronic devices that require excellent thermal conductivity and electrical insulation.

During plant embryogenesis, the apical-basal axis is established and both the shoot apical meristem (SAM) and the root apical meristem (RAM) are formed. In both meristems, there are slowly dividing cells which control the differentiation of their surrounding cells called the organizing centre (OC) and the quiescent centre (QC) in the shoot and root, respectively. These centres with their surrounding initial cells form a 'stem cell niche'. The initial cells eventually differentiate into various plant tissues, giving rise to plant organs such as lateral shoots, flowers, leaves, and lateral roots. Plant hormones are important factors involved in the balance between cell division and differentiation such that plant growth and development are tightly controlled in space and time. No single hormone acts by itself in regulating the meristematic activity in the root meristem. Division and differentiation are controlled by interactions between several hormones. Intensive research on plant stem cells has focused on how cell division is regulated to form specific plant organs and tissues, how differentiation is controlled, and how stem cell fate is coordinated. In this review, recent knowledge pertaining to the role of plant hormones in maintaining root stem cells including the QC is summarized and discussed. Furthermore, we suggest diverse approaches to answering the main question of how root stem cells are regulated and maintained by plant hormones.

Certain peptides containing high percentage of cationic amino acids are known to efficiently translocate through the cell membrane. This principle was previously exploited for delivery of variety proteins. We had observed that various basic peptides of earlier studies, though not specifically use for gene delivery, contain DNA or RNA binding domains. In the present study, we reported on arginine peptides, which form DNA complexes that efficiently transfect various cell lines. The transfection abilities of the peptides were observed by green fluorescent protein (GFP) and beta-galactosidase gene expression in 293T, HeLa, Jurkat, and COS-7 cells. We found superior transfection activity of arginine peptides compared with commercially available efficient transfection agents. The expression of marker genes induced by arginine peptides was partially inhibited in the presence of heparan sulfate, chondroitin sulfate B and C, or both heparinase III and chondroitinase ABC. The transfection proficiency of these peptides was affected by endosomotropic reagent as well as low temperature (4 degrees C). Finally, we have investigated the potential of arginine peptides as a delivery agent for gene therapy, by attempting to deliver herpes simplex virus thymidine kinase (HSV-TK) gene into tumor cells. HSV-TK transfected tumor cells exhibited sensitivity to the antiviral drug ganciclovir (GCV), leading to cell death. Taken together, these data demonstrate that arginine peptide is proficient for transfection, indicating its potentially benefit to studies in gene therapy and gene delivery in a range of model organisms.

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Sugars play important roles in many aspects of plant growth and development, acting as both energy sources and signaling molecules. With the successful use of genetic approaches, the molecular components involved in sugar signaling have been identified and their regulatory roles in the pathways have been elucidated. Here, we describe novel mutants of Arabidopsis (Arabidopsis thaliana), named glucose insensitive growth (gig), identified by their insensitivity to high-glucose (Glc)-induced growth inhibition. The gig mutant displayed retarded growth under normal growth conditions and also showed alterations in the expression of Glc-responsive genes under high-Glc conditions. Our molecular identification reveals that GIG encodes the plastidial copper (Cu) transporter PAA1 (for P 1B -type ATPase 1). Interestingly, double mutant analysis indicated that in high Glc, gig is epistatic to both hexokinase1 (hxk1) and aba insensitive4 (abi4), major regulators in sugar and retrograde signaling. Under high-Glc conditions, the addition of Cu had no effect on the recovery of gig/paa1 to the wild type, whereas exogenous Cu feeding could suppress its phenotype under normal growth conditions. The expression of GIG/PAA1 was also altered by mutations in the nuclear factors HXK1, ABI3, and ABI4 in high Glc. Furthermore, a transient expression assay revealed the interaction between ABI4 and the GIG/PAA1 promoter, suggesting that ABI4 actively regulates the transcription of GIG/PAA1, likely binding to the CCAC/ACGT core element of the GIG/PAA1 promoter. Our findings indicate that the plastidial Cu transporter PAA1, which is essential for plastid function and/or activity, plays an important role in bidirectional communication between the plastid and the nucleus in high Glc.