Sustainable energy development: performance and prospects

Concerns about sustainability, and the harsh realities of environmental catastrophe, can be traced back at least 4000 years. This paper points out how human pressures on the surrounding environment have had severe consequences over this period, coal burning has had adverse consequences traceable over the past 750 years, and the adverse environmental impacts of using other fossil fuels have aroused attention more recently. Heightened awareness of the need for sustainable development is a modern development, evident in international and national debates since the early 1970s. With the Brundtland Commission report published in 1987 came a framework for sustainable energy development. However, performance under the four elements of that framework have been almost uniformly disappointing. Fossil fuel use has continued to rise; renewable energy use has made insufficient inroads; waste and inefficiency in energy usage continues to be far too high; too many people remain without modern energy services or are exposed to severe pollution in the home and local atmosphere; there are mounting concerns about the conventional oil resource base—and future supplies and prices of oil and natural gas; greenhouse gas emissions continue to rise and evidence of human-induced climate change continues to mount. Indices of national environmental performance suggest no country is performing adequately; population, housing and transportation pressures result in greater pollution, loss of natural habitats, and species reduction; and poor governance is frequently cited as a major cause of poor environmental performance. The prospects for sustainable energy are bleak on current trends.     

Dynamic financial planning: certainty equivalents, stochastic constraints and functional conjugate duality

This paper studies portfolios under risk and stochastic constraints. Certainty equivalents combine risk aversion and exponential utility to form the objective. Budget and stochastic constraints on the account balance are used to ensure a positive net worth over time. These portfolio models are analyzed by functional conjugate duality for general distributions and by conjugate duality for the normal distribution. All the programs are convex. The duals provide insight into this approach and relate it to other stochastic and financial concepts.     

The effectiveness and safety of vaccines against human anthrax: a systematic review

We report on the results of a systematic review of existing controlled clinical trials undertaken to assess the effectiveness and safety of vaccines against human anthrax in relation to disease incidence and side-effects. Two articles retrieved by electronic and hand search fulfilling some of the inclusion criteria underwent a quality assessment by a group of reviewers. Data synthesized from the two trials showed that estimates of overall effectiveness and safety favour treatment (overall odds ratio 0.16; 95% confidence interval 0.07-0.34). The route of inoculation appears to make little difference to the effectiveness of the vaccines; however, one study shows that the incidence and severity of side-effects are significantly higher with the killed vaccine than with the alum-based placebo (overall odds ratio 0.16; 95% confidence interval 2.38-27.17).     

On The Feasibility of Imaging,By High Resolution Electron Microscopy,Isolated Individual Sheets of Graphitic Carbon

A comparative survey of computer simulated and experimentally obtained images shows that it is feasible to observe, end-on, isolated single sheets of trigonally bonded carbon atoms in graphitic substances directly by electron microscopy, provided that certain imaging conditions are employed. For a typical commercial instrument (Philips EM300 with a spherical aberration coefficient of 1.6 mm) authentic images are found whenever the objective lens is set at underfocus positions between 65 and 110 nm, with optimum contrast occurring near the ‘Scherzer’ imaging condition of 95 nm underfocus. At this latter focus position the fringe contrast is maximal when the sheet extends in the direction of the electron beam for a distance of about 5.5 nm; but sheets as narrow as 1.0 nm (i.e. containing some four widths of benzene rings in the direction of the electron beam) should be detectable.     

Ether lipids inhibit the effects of phorbol diester tumor promoters

Recent studies have shown that the tumor promoter 12-O-tetradecanoyl-phorbol-13-acetate (TPA) stimulates protein kinase C (PKC), whereas the ether-linked phospholipid 1-O-octadecyl-2-O-methyl-rac-glycerol-3-phosphocholine (ET-18-OCH₃) inhibits PKC activity in vitro. Therefore, the antitumor effects of ET-18-OCH₃ could be due to its inhibition of PKC activity and the effects of tumor promotion. TPA stimulates arachidonic acid release, prostaglandin synthesis, phosphatidylcholine synthesis and the degradation of phosphatidylcholine by phospholipase C in Madin Darby canine kidney (MDCK) cells. Therefore, we have determined the effects of ET-18-OCH₃ on these consequences of TPA stimulation. Preliminary experiments determined that ET-18-OCH₃ inhibited PKC partially purified from MDCK cells by ion-exchange chromatography on DEAE-cellulose. In addition, ET-18-OCH₃, inhibited the TPA-stimulated phosphorylation of a 40,000-dalton protein in intact MDCK cells. These data indicate that ET-18-OCH₃ is an effective inhibitor of PKC activity in MDCK cells. In addition, ET-18-OCH₃ was found to inhibit arachidonic acid release and prostaglandin synthesis. The inhibition of prostaglandin synthesis appears to be secondary to inhibition of arachidonic acid release, since ET-18-OCH₃ does not inhibit TPA-stimulated synthesis of prostaglandin H synthase or the activity of the enzyme directly (Parker, J., Daniel, L. W., and Waite, M. [1987]J. Biol. Chem. 262, 5385–5393). ET-18-OCH₃ also inhibits TPA-stimulated phosphatidylcholine synthesis and phosphatidylcholine degradation by phospholipase C. These data provide evidence that the antineoplastic ether lipids inhibit the biochemical effects of the tumor promoter TPA in intact cells and indicate that this inhibition may have a role in their biological activities.     

A novel phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase associates with the interleukin-3 receptor

To gain insight into the intracellular signaling cascades that are activated by the binding of interleukin-3 (IL-3) to its target cells, we have embarked on the identification of proteins that are associated with the IL-3 receptor (IL-3R). In a previous study we reported that a 110-kDa serine/threonine protein kinase is constitutively associated with the IL-3R and activated following IL-3 stimulation. We now report that a phosphatidylinositol-3,4, 5-trisphosphate (PtdIns-3,4,5-P3) 5-phosphatase (5-ptase) is also constitutively associated with the IL-3R. This 5-ptase is magnesium-dependent and removes the 5-position phosphate from PtdIns-3,4,5-P3 but does not metabolize PtdIns-4,5-P2, inositol (Ins)-1,3,4,5-P4, or Ins-1,4,5-P3. This substrate specificity distinguishes it from any previously characterized 5-ptase. Interestingly, it may be bound indirectly via phosphatidylinositol 3-kinase (PI 3-kinase), another enzyme that is constitutively bound to the IL-3R. However, unlike PI 3-kinase which becomes activated following IL-3 stimulation, this receptor-associated 5-ptase activity does not increase following IL-3 stimulation, and its primary function may be to keep the principal in vivo product of PI 3-kinase, PtdIns-3,4,5-P3, at low levels in unstimulated cells, to terminate the PI 3-kinase signal following IL-3 stimulation or to metabolize PtdIns-3,4,5-P3 to a metabolically active second messenger, i.e. PtdIns-3,4-P2.     

<Emphasis Type="Italic">Arabidopsis thaliana:</Emphasis> A New Test Species for Phytotoxic Bioassays

Lettuce seeds (Lactuca sativa L.) and other crop species are often used in phytotoxic bioassays that are designed to detect allelochemicals. The seeds of these species are considered ideal because they are readily available, germinate rapidly and uniformly, and are routinely used in laboratories around the world. Despite their common use, however, the seeds of these species are often not as sensitive or responsive to some phytotoxic chemicals as are the seeds of other species. While searching for a more sensitive test species for phytotoxic bioassays, the Columbia ecotype of Arabidopsis thaliana exhibited greater sensitivity to seven potent allelochemicals than did lettuce seeds, which, in some cases, did not respond at all to those substances. Sensitivity satisfies one of the criteria for selecting a test species for bioassays. We now report on the results of our study and offer additional reasons for using A. thaliana seeds.     

Lattice imaging of structural defects in a chain silicate: The pyroxenoid mineral rhodonite

The pyroxenoid mineral rhodonite has been examined by electron diffraction and high-resolution lattice imaging. Planar defects parallel to (110) and (001) have been observed. The former are comparable to the (100) stacking faults frequently observed in the related mineral wollastonite, whereas the latter involve unit cell strips of the more complex pyroxmangite structure occasionally inserted into the parent rhodonite matrix.     

Multigram synthesis of 1-alkylamido phospholipids

Phospholipids containing a 1-alkylamido linkage have shown promisingin vitro neoplastic cell growth inhibitory properties and anti-human immunodeficiency viral activity. We have synthesized a series of alkylamido ether lipid analogues on a milligram scale for initial evaluation, but for furtherin vivo testing of these bioactive phospholipids, synthesis on a larger scale is required. The multigram synthesis of 1-alkylamido ether phospholipids was accomplished by modifying reaction conditions in the amidation step and changing reagents and solvent systems in both the detritylation and phosphorylation steps. This was most crucial in the phosphorylation step, where in the multigram synthesis 2-bromoethyl dichlorophosphate in diethyl ether/tetrahydrofuran (7∶3, vol/vol) gave much improved yields as compared to the 2-chloro-2-oxo-1,3,2-dioxaphospholane reagent. The modifications also resulted in a product that could be more easily purified in sufficient quantities for use inin vivo inhibition studies.     

Nanocomposite powders of hydroxyapatite-graphene oxide for biological applications

The repair of bone fractures is a clinical challenge for patients with impaired healing, such as osteoporosis. Currently, different strategies have been developed to design new biomaterials, enhancing their interactions with biological systems and conducting the cellular behavior in the desired direction to help fracture healing. In the present work, hydroxyapatite-graphene oxide (HA-GO) nanocomposites were produced and the morphological and physicochemical influences of the addition of 0.5 wt%, 1.0 wt% and 1.5 wt% of GO to HA were observed. FEG-SEM and TEM analyses of HA-GO nanocomposites showed HA nanoparticles adhered to the surface of the GO sheets, suggesting an effective method to form nanostructured graphene-based biomaterials. As confirmation, physicochemical analyses by Raman, FTIR and TGA demonstrated a strong affinity between HA and GO, according to the increase of concentration from 0.5 wt% to 1.5 wt% GO in the HA-GO nanocomposites. Also, in order to evaluate the HA-GO nanocomposites behavior under biological microenvironment, in vitro bioactivity and indirect cytotoxicity tests were performed. FEG-SEM analyses confirmed the positive results for the bioactivity properties of HA-GO nanocomposite and indirect cytotoxicity demonstrated that even with a decrease in the hDPSCs viability and proliferation, when increasing to 1.5 wt% of GO concentration, high level of cell viability was exhibited by HA-GO nanocomposites. These biological results suggested the 0.5 wt% HA-GO nanocomposite as a potential bioactive bone graft and a promising biomaterial for bone tissue regeneration, when compared to the pure HA.