Alternative Substrates and Fertilization Routine Relationships for Bedding Pot Plants: Impatiens wallerana

This study was carried out searching for alternative substrates to traditional peat based on river waste and Sphagnum and Carex peat from Argentinean peatlands and used to grow Impatiens wallerana bedding plant. The aim of this study was i) to characterize physical and chemical effects from seven growing media on I. wallerana plants grown under different fertilization rates and ii) to describe the physiological mechanisms in plants, involved in the use of such substrates. Particle stability was lower for the six alternative substrates compared to the Canadian peat-base control substrate. However, with a high fertilization dose it is possible to reach non significant differences in plant growth compared to the control substrate. It is suggested, for future research, that nitrogen signalling associated to cytokinin synthesis by roots is involved.Fil: Thibaud, J.. Universidad de Buenos Aires. Facultad de Agronomia. Departamento de Producción Vegetal. Cátedra de Floricultura; ArgentinaFil: Loughlin, T. Mc.. Universidad de Buenos Aires. Facultad de Agronomia. Departamento de Producción Vegetal. Cátedra de Floricultura; ArgentinaFil: Pagani, A.. Universidad de Buenos Aires. Facultad de Agronomia. Departamento de Producción Vegetal. Cátedra de Floricultura; ArgentinaFil: Lavado, Raul Silvio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Biociencias Agrícolas y Ambientales. Universidad de Buenos Aires. Facultad de Agronomía. Instituto de Investigaciones en Biociencias Agrícolas y Ambientales; ArgentinaFil: Di Benedetto, Adalberto Hugo. Universidad Nacional de Mar del Plata. Facultad de Ciencias Agrarias; Argentina. Universidad de Buenos Aires. Facultad de Agronomia. Departamento de Producción Vegetal. Cátedra de Floricultura; Argentin

An interdisciplinary approach to volcanic risk reduction under conditions of uncertainty: a case study of Tristan da Cunha

The uncertainty brought about by intermittent volcanic activity is fairly common at volcanoes worldwide. While better knowledge of any one volcano's behavioural characteristics has the potential to reduce this uncertainty, the subsequent reduction of risk from volcanic threats is only realised if that knowledge is pertinent to stakeholders and effectively communicated to inform good decision making. Success requires integration of methods, skills and expertise across disciplinary boundaries. This research project develops and trials a novel interdisciplinary approach to volcanic risk reduction on the remote volcanic island of Tristan da Cunha (South Atlantic). For the first time, volcanological techniques, probabilistic decision support and social scientific methods were integrated in a single study. New data were produced that (1) established no spatio-temporal pattern to recent volcanic activity; (2) quantified the high degree of scientific uncertainty around future eruptive scenarios; (3) analysed the physical vulnerability of the community as a consequence of their geographical isolation and exposure to volcanic hazards; (4) evaluated social and cultural influences on vulnerability and resilience; and (5) evaluated the effectiveness of a scenario planning approach, both as a method for integrating the different strands of the research and as a way of enabling on-island decision makers to take ownership of risk identification and management, and capacity building within their community. The paper provides empirical evidence of the value of an innovative interdisciplinary framework for reducing volcanic risk. It also provides evidence for the strength that comes from integrating social and physical sciences with the development of effective, tailored engagement and communication strategies in volcanic risk reduction

A multi-well plate model of reactive gliosis for high throughput screening of potential CNS therapies

Reactive astrogliosis is an important feature of CNS damage and disease which involves changes in astrocyte phenotype and morphology. In particular, CNS trauma can lead to the formation of a glial scar, a three dimensional (3D) mesh of astrocyte processes that can form a physical and chemical barrier to neuronal regeneration, which is a potential target for CNS drug and cell therapy. However, reactive gliosis is difficult to isolate and monitor in typical animal models of CNS damage. In monolayer culture systems astrocytes adopt a highly reactive phenotype, limiting the range of available models suitable for research in this area. Our previous 3D cell culture systems allow astrocytes to be maintained with a relatively unreactive phenotype until stimulated, whereupon a classical reactive astrocyte response can be monitored. The aim of the current work is to adapt this approach in order to develop a multi-well plate system to provide a reliable, consistent model of reactive gliosis for high throughput screening and research. Once baseline viability and phenotype of primary rat astrocytes were investigated in these models, reactivity was triggered using treatments such as TGFβ1, as seen in Figure 1, hypoxia and low glucose. Outputs included confocal microscopy and 3D image analysis, Western blotting and RT-PCR to quantify markers such as GFAP and CSPG in test and control gels. Using GFP-labelled astrocytes permitted monitoring of cytoplasmic volume and shape, giving an additional measure of astrocyte hypertrophic response within stimulated conditions. The robust protocol that we have developed can form a basis to investigate astrocyte biology in a highly controlled environment, and to model phenotypic features of astrocytes in both damaged and undamaged CNS. A reproducible multi-well plate system will provide an experimental platform which allows potential CNS therapies to be screened at high-throughput, and the effects of potential modulators of astrocyte reactivity to be investigated simply and systematically

Microscopic biophysical model of self-organization in tissue due to feedback between cell- and macroscopic-scale forces

We develop a microscopic biophysical model for self-organization and reshaping of artificial tissue, that is codriven by microscopic active forces between cells and an extracellular matrix (ECM), and macroscopic forces that develop within the tissue, finding close agreement with experiment. Microscopic active forces are stimulated by μm-scale interactions between cells and the ECM within which they exist, and when large numbers of cells act together these forces drive, and are affected by, macroscopic-scale self-organization and reshaping of tissues in a feedback loop. To understand this loop, there is a need to (1) construct microscopic biophysical models that can simulate these processes for the very large number of cells found in tissues, (2) validate and calibrate those models against experimental data, and (3) understand the active feedback between cells and the extracellular matrix, and its relationship to macroscopic self-organization and reshaping of tissue. Our microscopic biophysical model consists of a contractile network representing the ECM, that interacts with a large number of cells via dipole forces, to describe macroscopic self-organization and reshaping of tissue. We solve the model using simulated annealing, finding close agreement with experiments on artificial neural tissue. We discuss the calibration of model parameters. We conclude that feedback between microscopic cell-ECM dipole interactions and tissue-scale forces is a key factor in driving macroscopic self-organization and reshaping of tissue. We discuss the application of the biophysical model to the simulation and rational design of artificial tissues

Molybdenum dioxide in carbon nanoreactors as a catalytic nanosponge for the efficient desulfurization of liquid fuels

The principle of a “catalytic nanosponge” that combines the catalysis of organosulfur oxidation and sequestration of the products from reaction mixtures is demonstrated. Group VI metal oxide nanoparticles (CrOx, MoOx, WOx) are embedded within hollow graphitized carbon nanofibers (GNFs), which act as nanoscale reaction vessels for oxidation reactions used in the decontamination of fuel. When immersed in a model liquid alkane fuel contaminated with organosulfur compounds (benzothiophene, dibenzothiophene, dimethyldibenzothiophene), it is found that MoO2@GNF nanoreactors, comprising 30 nm molybdenum dioxide nanoparticles grown within the channel of GNFs, show superior abilities toward oxidative desulfurization (ODS), affording over 98% sulfur removal at only 5.9 mol% catalyst loading. The role of the carbon nanoreactor in MoO2@GNF is to enhance the activity and stability of catalytic centers over at least 5 cycles. Surprisingly, the nanotube cavity can selectively absorb and remove the ODS products (sulfoxides and sulfones) from several model fuel systems. This effect is related to an adsorptive desulfurization (ADS) mechanism, which in combination with ODS within the same material, yields a “catalytic nanosponge” MoO2@GNF. This innovative ODS and ADS synergistic functionality negates the need for a solvent extraction step in fuel desulfurization and produces ultralow sulfur fuel

Engineered neural tissue for peripheral nerve repair

A new combination of tissue engineering techniques provides a simple and effective method for building aligned cellular biomaterials. Self-alignment of Schwann cells within a tethered type-1 collagen matrix, followed by removal of interstitial fluid produces a stable tissue-like biomaterial that recreates the aligned cellular and extracellular matrix architecture associated with nerve grafts. Sheets of this engineered neural tissue supported and directed neuronal growth in a co-culture model, and initial in vivo tests showed that a device containing rods of rolled-up sheets could support neuronal growth during rat sciatic nerve repair (5 mm gap). Further testing of this device for repair of a critical-sized 15 mm gap showed that, at 8 weeks, engineered neural tissue had supported robust neuronal regeneration across the gap. This is, therefore, a useful new approach for generating anisotropic engineered tissues, and it can be used with Schwann cells to fabricate artificial neural tissue for peripheral nerve repair