New bioassays reveal susceptibility of stone-fruit rootstocks to capnodis tenebrionis larvae

Larvae of Capnodis tenebrionis (L.) (Coleoptera Buprestidae) feed and develop in roots of stone-fruit trees, thereby decreasing their efficiency, which can lead to plant death. The control of these larvae is critical, due to their localization in the root, and the management of this pest is focused on adults, mainly by using non-specific synthetic insecticides. Less susceptible Prunus rootstocks might be applied as a preventative management of larval infestation by this pest. The current research investigated the susceptibility to C. tenebrionis larvae of the most commonly used rootstocks by combining two bio-assays during two-year trials: development of larvae assayed on semi-artificial substrates containing rootstock bark flour; infestation by neonate larvae on rootstock twigs. The rearing assay on semi-artificial substrates made it possible to distinguish (1) a rootstock cluster (Montclar and GF677) in which larvae developed faster and heavier and produced larger adults, (2) a cluster (Adesoto, CAB6P, Colt and MaxMa60) in which larval growth was less efficient as well as adult size, and (3) a cluster (Garnem and Myrabolan 29C) with intermediate responses in larval development and adult size. The twig infestation assay by neonates showed the most infested (Colt) and least infested (Barrier, MaxMa60 and Marianna 26) rootstocks. When the results of both assays are combined, GF677 and Myrabolan 29C appear more susceptible, while Adesoto and MaxMa60 less susceptible to C. tenebrionis larvae, although Barrier and Marianna 26 require further investigation. The experimental model applied in the current trials can enable processing of a large number of tests on different rootstocks, thereby allowing the accumulation of a large quantity of data on the potential susceptibility of rootstocks. The possibility of rearing larvae on a substrate can allow comparison of additional compounds that could interact with larval growth

Influence of molecular processes on the hydrogen atomic system in an expanding argon-hydrogen plasma

An expanding thermal arc plasma in argon–hydrogen is investigated by means of emission spectroscopy. The hydrogen can be added to the argon flow before it enters the thermal arc plasma source, or it can be flushed directly into the vacuum expansion vessel (1–20 vol¿% H2). The atomic state distribution function for hydrogen, measured at a downstream distance of 20 mm, turns out to be very different in the two cases. For injection in the arc, three-particle recombination is a primary source of hydrogen excitation, whereas measurements with hydrogen injected into the vessel clearly point to a molecular channel (dissociative recombination of formed ArH+) populating atomic hydrogen levels

The design and commissioning of the MICE upstream time-of-flight system

In the MICE experiment at RAL the upstream time-of-flight detectors are used for particle identification in the incoming muon beam, for the experiment trigger and for a precise timing (sigma_t ~ 50 ps) with respect to the accelerating RF cavities working at 201 MHz. The construction of the upstream section of the MICE time-of-flight system and the tests done to characterize its individual components are shown. Detector timing resolutions ~50-60 ps were achieved. Test beam performance and preliminary results obtained with beam at RAL are reported.Comment: accepted on Nuclear Instruments and Methods

Multi-step exploitation of raw arundo donax L. For the selective synthesis of second-generation sugars by chemical and biological route

Lignocellulosic biomass represents one of the most important feedstocks for future biorefineries, being a precursor of valuable bio-products, obtainable through both chemical and biological conversion routes. Lignocellulosic biomass has a complex matrix, which requires the careful development of multi-step approaches for its complete exploitation to value-added compounds. Based on this perspective, the present work focuses on the valorization of hemicellulose and cellulose fractionsof giant reed (Arundo donax L.) to give second-generation sugars, minimizing the formation of reaction by-products. The conversion of hemicellulose to xylose was undertaken in the presence of the heterogeneous acid catalyst Amberlyst-70 under microwave irradiation. The effect of the main reaction parameters, such as temperature, reaction time, catalyst, and biomass loadings on sugars yield was studied, developing a high gravity approach. Under the optimised reaction conditions (17 wt% Arundo donax L. loading, 160 °C, Amberlyst-70/Arundo donax L. weight ratio 0.2 wt/wt), the xylose yield was 96.3 mol%. In the second step, the cellulose-rich solid residue was exploited through the chemical or enzymatic route, obtaining glucose yields of32.5 and56.2 mol%, respectively. This work proves the efficiency of this innovative combination of chemical and biological catalytic approaches, for the selective conversion of hemicellulose and cellulose fractions of Arundo donax L. to versatile platform products

Optimized conversion of wheat straw into single cell oils by Yarrowia lipolytica and Lipomyces tetrasporus and synthesis of advanced biofuels

This paper deals with the optimized conversion of undetoxified wheat straw hydrolysates into microbial lipids by two oleaginous yeasts, Yarrowia lipolytica and Lipomyces tetrasporus. Wheat straw were pretreated by steam explosion at 203 degrees C for 300 s and hydrolysed at 20% solid-to-liquid ratio by using an enzymatic loading of 15 FPU/ g substrate. The mixed wheat straw hydrolysates (WHS) contained 86 gL-1 glucose and 22 gL-1 xylose, 2.3 gL-1 acetic acid, 0.9 gL-1 furanic compounds. The fermentation process was optimized in terms of the inoculum age and density, medium composition, and bioreactor feeding strategy. In particular, the different capacity of the two yeasts to overcome the toxic effect of the biomass degradation by-products, in different inoculum ages, was deeply investigated. Two hydrolysates concentration were tested: WSH containing 86 gL-1 glucose and 22 gL-1 xylose and the diluted medium containing 40 gL-1 glucose and 22 gL-1 xylose. The results indicated that both yeasts were able to detoxify WSH and grow on undetoxified hydrolysates as effect of the intrinsic capacity to metabolize the furan derivatives. Y. lipolytica was able to detoxify the medium in all the investigated set-ups, while L. tetrasporus was able to detoxify the medium only if inoculated in the stationary phase of growth. After the process optimization in shaken flasks, the production of Single Cell Oils (SCOs) by L. tetrasporus was carried out in a medium-scale bioreactor of 10L obtaining lipid yield and cell content of 21% and 62%, respectively. The extracted SCOs, with high oleic and palmitic acid content, were converted into biodiesel displaying overall features in accordance with international biodiesel standards, namely ASTM and EN 14214

Differential cartilaginous tissue formation by human synovial membrane, fat pad, meniscus cells and articular chondrocytes

Objective: To identify an appropriate cell source for the generation of meniscus substitutes, among those which would be available by arthroscopy of injured knee joints. Methods: Human inner meniscus cells, fat pad cells (FPC), synovial membrane cells (SMC) and articular chondrocytes (AC) were expanded with or without specific growth factors (Transforming growth factor-betal, Fibroblast growth factor-2 and Plate let-derived growth factor bb, TFP) and then induced to form three-dimensional cartilaginous tissues in pellet cultures, or using a hyaluronan-based scaffold (Hyaff(R)-11), in culture or in nude mice. Human native menisci were assessed as reference. Results: Cell expansion with TFP enhanced glycosaminoglycan (GAG) deposition by all cell types (up to 4.1-fold) and messenger RNA expression of collagen type II by FPC and SMC (up to 472-fold) following pellet culture. In all models, tissues generated by AC contained the highest fractions of GAG (up to 1.9 were positively stained for collagen type II (specific of the inner avascular region of meniscus), type IV (mainly present in the outer vascularized region of meniscus) and types I, III and VI (common to both meniscus regions). Instead, inner meniscus, FPC and SMC developed tissues containing negligible GAG and no detectable collagen type II protein. Tissues generated by AC remained biochemically and phenotypically stable upon ectopic implantation. Conclusions: Under our experimental conditions, only AC generated tissues containing relevant amounts of GAG and with cell phenotypes compatible with those of the inner and outer meniscus regions. Instead, the other investigated cell sources formed tissues resembling only the outer region of meniscus. It remains to be determined whether grafts based on AC will have the ability to reach the complex structural and functional organization typical of meniscus tissue. (C) 2006 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights rese

Active-Sterile neutrino oscillations and BBN+CMBR constraints

We show how active-sterile neutrino oscillations in the early Universe can play an interesting role in explaining the current observations of CMBR anisotropies and light element abundances. We describe different possible phenomenological scenarios in the interpretation of present data and how active-sterile neutrino oscillations can provide a viable theoretical framework.Comment: Some changes, to appear in Phys. Rev.

VHMPID: a new detector for the ALICE experiment at LHC

This article presents the basic idea of VHMPID, an upgrade detector for the ALICE experiment at LHC, CERN. The main goal of this detector is to extend the particle identification capabilities of ALICE to give more insight into the evolution of the hot and dense matter created in Pb-Pb collisions. Starting from the physics motivations and working principles the challenges and current status of development is detailed.Comment: 4 pages, 6 figures. To be published in EPJ Web of Conference