Temporal Control over Transient Chemical Systems using Structurally Diverse Chemical Fuels

The next generation of adaptive, intelligent chemical systems will rely on a continuous supply of energy to maintain the functional state. Such systems will require chemical methodology that provides precise control over the energy dissipation process, and thus, the lifetime of the transiently activated function. This manuscript reports on the use of structurally diverse chemical fuels to control the lifetime of two different systems under dissipative conditions: transient signal generation and the transient formation of self-assembled aggregates. The energy stored in the fuels is dissipated at different rates by an enzyme, which in-stalls a dependence of the lifetime of the active system on the chemical structure of the fuel. In the case of transient signal generation, it is shown that different chemical fuels can be used to generate a vast range of signal profiles, allowing temporal control over two orders of magnitude. Regarding self-assembly under dissipative conditions, the ability to control the lifetime using different fuels turns out to be particularly important as stable aggregates are formed only at well-defined surfactant/fuel ratios, meaning that temporal control cannot be achieved by simply changing the fuel concentration

The Interrelations between a Multi-Layered Coastal Aquifer, a Surface Reservoir (Fish Ponds), and the Sea

This research examines the interrelations in a complex hydrogeological system, consisting of a multi-layered coastal aquifer, the sea, and a surface reservoir (fish ponds) and the importance of the specific connection between the aquifer and the sea. The paper combines offshore geophysical surveys (CHIRP) and on land TDEM (Time Domain Electro Magnetic), together with hydrological measurements and numerical simulation. The Quaternary aquifer at the southern Carmel plain is sub-divided into three units, a sandy phreatic unit, and two calcareous sandstone (‘Kurkar’) confined units. The salinity in the different units is affected by their connection with the sea. We show that differences in the seaward extent of its clayey roof, as illustrated in the CHIRP survey, result in a varying extent of seawater intrusion due to pumping from the confined units. FEFLOW simulations indicate that the FSI (Fresh Saline water Interface) reached the coastline just a few years after pumping has begun, where the roof terminates ~100 m from shore, while no seawater intrusion occurred in an area where the roof is continuous farther offshore. This was found to be consistent with borehole observations and TDEM data from our study sites. The water level in the coastal aquifer was generally stable with surprisingly no indication for significant seawater intrusion although the aquifer is extensively pumped very close to shore. This is explained by contribution from the underlying Late Cretaceous aquifer, which increased with the pumping rate, as is also indicated by the numerical simulations

Predicting the vulnerability of great apes to disease : the role of superspreaders and their potential vaccination

Charlotte Carne was funded by a scholarship from the University of Roehampton (http://www.roehampton.ac.uk/home/). The Royal Zoological Society of Scotland (http://www.rzss.org.uk/) provided core funding for the Budongo Conservation Field Station. The orang-utan field research was funded by the Wildlife Conservation Society (WCS: http://www.wcs.org/), the US Fish and Wildlife Service Great Ape Conservation Fund (http://www.fws.gov/international/wildlif​e-without-borders/great-ape-conservation​-fund.html), Orang-utan Tropical Peatland Project (OuTrop: http://www.outrop.com/), Primate Conservation Inc. (http://www.primate.org/), and the L.S.B. Leakey Foundation (http://leakeyfoundation.org/).Disease is a major concern for the conservation of great apes, and one that is likely to become increasingly relevant as deforestation and the rise of ecotourism bring humans and apes into ever closer proximity. Consequently, it is imperative that preventative measures are explored to ensure that future epidemics do not wipe out the remaining populations of these animals. In this paper, social network analysis was used to investigate vulnerability to disease in a population of wild orang-utans and a community of wild chimpanzees. Potential 'superspreaders' of disease - individuals with disproportionately central positions in the community or population - were identified, and the efficacy of vaccinating these individuals assessed using simulations. Three resident female orang-utans were identified as potential superspreaders, and females and unflanged males were predicted to be more influential in disease spread than flanged males. By contrast, no superspreaders were identified in the chimpanzee network, although males were significantly more central than females. In both species, simulating the vaccination of the most central individuals in the network caused a greater reduction in potential disease pathways than removing random individuals, but this effect was considerably more pronounced for orang-utans. This suggests that targeted vaccinations would have a greater impact on reducing disease spread among orang-utans than chimpanzees. Overall, these results have important implications for orang-utan and chimpanzee conservation and highlight the role that certain individuals may play in the spread of disease and its prevention by vaccination.Publisher PDFPeer reviewe

Spectral and redox characterization of the heme c(i) of the cytochrome b(6)f complex

Absorption spectra of the purified cytochrome b(6)f complex from Chlamydomonas reinhardtii were monitored as a function of the redox potential. Four spectral and redox components were identified: in addition to heme f and the two b hemes, the fourth component must be the new heme c(i) (also denoted x) recently discovered in the crystallographic structures. This heme is covalently attached to the protein, but has no amino acid axial ligand. It is located in the plastoquinone-reducing site Q(i) in the immediate vicinity of a b heme. Each heme titrated as a one-electron Nernst curve, with midpoint potentials at pH 7.0 of -130 mV and -35 mV (hemes b), +100 mV (heme c(i)), and +355 mV (heme f). The reduced minus oxidized spectrum of heme c(i) consists of a broad absorption increase centered ≈425 nm. Its potential has a dependence of -60 mV/pH unit, implying that the reduced form binds one proton in the pH 6-9 range. The Q(i) site inhibitor 2-n-nonyl-4-hydroxyquinoline N-oxide, a semiquinone analogue, induces a shift of this potential by about -225 mV. The spectrum of c(i) matches the absorption changes previously observed in vivo for an unknown redox center denoted “G.” The data are discussed with respect to the effect of the membrane potential on the electron transfer equilibrium between G and heme b(H) found in earlier experiments

Establishment of transplantable porcine tumor cell lines derived from MHC- inbred miniature swine

The lack of transplantable tumors has limited assessment of graft-versus-tumor effects following hematopoietic cell transplantation in clinically relevant large-animal models. We describe the derivation and characterization of porcine tumor cell lines with initial efforts of tumor transplantation using immunocompromised mice and highly inbred sublines of Massachusetts General Hospital major histocompatibility complex (MHC)–inbred miniature swine. Autopsies were performed routinely on swine that died unexpectedly or had suspicion of malignancy based on clinical symptoms or peripheral blood analysis. Tissue samples were obtained for pathology, phenotyped by flow cytometry, and placed in culture. Based on growth, lines were selected for passage into nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice and miniature swine. Porcine tumor recipients were preconditioned with total body irradiation from 0 to 500 cGy or with a 30-day course of oral cyclosporine. We identified 19 cases of hematologic tumors. Nine distinct tumor cell lines were established from 8 of these cases, including 3 derived from highly inbred sublines. In vivo tumor growth and serial transfer were observed in immunocompromised mice for one tumor cell line and in miniature swine for 1 of 2 tumor cell lines expanded for this purpose. These results suggest the possibility of developing a transplantable tumor model in this large-animal system