3,133 research outputs found

    Adsorption and desorption dynamics of citric acid anions in soil

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    The functional role of organic acid anions (e.g. citrate, oxalate, malonate, etc) in soil has been intensively investigated with special focus either on (i) microbial respiration and soil carbon dynamics, (ii) nutrient solubilization, or (iii) metal detoxification. Considering the potential impact of sorption processes on the functional significance of these effects, comparatively little is known about the adsorption and desorption dynamics of organic acid anions in soils. The aim of this study therefore was to experimentally characterize the adsorption and desorption dynamics of organic acid anions in different soils using citrate as a model carboxylate. Results showed that both adsorption and desorption processes were fast, reaching a steady state equilibrium solution concentration within approximately 1 hour. However, for a given total soil citrate concentration(ctot) the steady state value obtained was critically dependent on the starting conditions of the experiment (i.e. whether most of the citrate was initially present in solution (cl) or held on the solid phase (cs)). Specifically, desorption-led processes resulted in significantly lower equilibrium solution concentrations than adsorption led processes indicating time-dependent sorption hysteresis. As it is not possible to experimentally distinguish between different sorption pools in soil (i.e. fast, slow, irreversible adsorption/desorption), a new dynamic hysteresis model was developed that relies only on measured soil solution concentrations. The model satisfactorily explained experimental data and was able to predict dynamic adsorption and desorption behaviour. To demonstrate its use we applied the model to two relevant scenarios (exudation and microbial degradation), where the dynamic sorption behaviour of citrate occurs. Overall, this study highlights the complex nature of citrate sorption in soil and concludes that existing models need to incorporate both a temporal and sorption hysteresis component to realistically describe the role and fate of organic acids in soil processes

    Constraints on the χ_(c1) versus χ_(c2) polarizations in proton-proton collisions at √s = 8 TeV

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    The polarizations of promptly produced χ_(c1) and χ_(c2) mesons are studied using data collected by the CMS experiment at the LHC, in proton-proton collisions at √s=8  TeV. The χ_c states are reconstructed via their radiative decays χ_c → J/ψγ, with the photons being measured through conversions to e⁺e⁻, which allows the two states to be well resolved. The polarizations are measured in the helicity frame, through the analysis of the χ_(c2) to χ_(c1) yield ratio as a function of the polar or azimuthal angle of the positive muon emitted in the J/ψ → μ⁺μ⁻ decay, in three bins of J/ψ transverse momentum. While no differences are seen between the two states in terms of azimuthal decay angle distributions, they are observed to have significantly different polar anisotropies. The measurement favors a scenario where at least one of the two states is strongly polarized along the helicity quantization axis, in agreement with nonrelativistic quantum chromodynamics predictions. This is the first measurement of significantly polarized quarkonia produced at high transverse momentum

    In vitro template-change PCR to create single crossover libraries: a case study with B. thuringiensis Cry2A toxins

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    During evolution the creation of single crossover chimeras between duplicated paralogous genes is a known process for increasing diversity. Comparing the properties of homologously recombined chimeras with one or two crossovers is also an efficient strategy for analyzing relationships between sequence variation and function. However, no well-developed in vitro method has been established to create single-crossover libraries. Here we present an in vitro template-change polymerase change reaction that has been developed to enable the production of such libraries. We applied the method to two closely related toxin genes from B. thuringiensis and created chimeras with differing properties that can help us understand how these toxins are able to differentiate between insect species

    Improving phylogeny reconstruction at the strain level using peptidome datasets

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    Typical bacterial strain differentiation methods are often challenged by high genetic similarity between strains. To address this problem, we introduce a novel in silico peptide fingerprinting method based on conventional wet-lab protocols that enables the identification of potential strain-specific peptides. These can be further investigated using in vitro approaches, laying a foundation for the development of biomarker detection and application-specific methods. This novel method aims at reducing large amounts of comparative peptide data to binary matrices while maintaining a high phylogenetic resolution. The underlying case study concerns the Bacillus cereus group, namely the differentiation of Bacillus thuringiensis, Bacillus anthracis and Bacillus cereus strains. Results show that trees based on cytoplasmic and extracellular peptidomes are only marginally in conflict with those based on whole proteomes, as inferred by the established Genome-BLAST Distance Phylogeny (GBDP) method. Hence, these results indicate that the two approaches can most likely be used complementarily even in other organismal groups. The obtained results confirm previous reports about the misclassification of many strains within the B. cereus group. Moreover, our method was able to separate the B. anthracis strains with high resolution, similarly to the GBDP results as benchmarked via Bayesian inference and both Maximum Likelihood and Maximum Parsimony. In addition to the presented phylogenomic applications, whole-peptide fingerprinting might also become a valuable complementary technique to digital DNA-DNA hybridization, notably for bacterial classification at the species and subspecies level in the future.This research was funded by Grant AGL2013-44039-R from the Spanish “Plan Estatal de I+D+I”, and by Grant EM2014/046 from the “Plan Galego de investigación, innovación e crecemento 2011-2015”. BS was recipient of a Ramón y Cajal postdoctoral contractfrom the Spanish Ministry of Economyand Competitiveness. This work was also partially funded by the [14VI05] Contract-Programme from the University of Vigo and the Agrupamento INBIOMED from DXPCTSUG-FEDER unha maneira de facer Europa (2012/273).The research leading to these results has also received funding from the European Union’s Seventh Framework Programme FP7/REGPOT-2012-2013.1 under grant agreement n˚ 316265, BIOCAPS. This document reflects only the authors’ views and the European Union is not liable for any use that may be made of the information contained herein. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

    Provisioning of data locality for HEP analysis workflows

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    The heavily increasing amount of data produced by current experiments in high energy particle physics challenge both end users and providers of computing resources. The boosted data rates and the complexity of analyses require huge datasets being processed in short turnaround cycles. Usually, data storages and computing farms are deployed by different providers, which leads to data delocalization and a strong influence of the interconnection transfer rates. The CMS collaboration at KIT has developed a prototype enabling data locality for HEP analysis processing via two concepts. A coordinated and distributed caching approach that reduce the limiting factor of data transfers by joining local high performance devices with large background storages were tested. Thereby, a throughput optimization was reached by selecting and allocating critical data within user work-flows. A highly performant setup using these caching solutions enables fast processing of throughput dependent analysis workflows
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