Relative response of TL and component-resolved OSL to alpha and beta radiations in annealed sedimentary quartz

Knowledge of the relative luminescence response to alpha and beta radiation is very important in TL and OSL dating. In the present study the relative alpha to beta response is studied in a sedimentary quartz sample, previously fired at 900 °C for 1 h, in the dose region between 1 and 128 Gy, for both thermoluminescence (TL) and linearly modulated optically stimulated luminescence (LM – OSL). The LM – OSL measurements were performed at room temperature and at 125 °C. All OSL signals were deconvolved into their individual components. Comparison of OSL curves after alpha and beta irradiation strongly supports that quartz OSL components follow first order kinetics in both cases. In the case of TL, the relative alpha to beta response is found to be very different for each TL glow-peak, but it does not depend strongly on irradiation dose. In the case of LM – OSL measurements, it is found that the relative behaviour of the alpha to beta response is different for three distinct regions, namely the fast OSL component, the region of medium OSL component originating from the TL glow-peak at 110 °C when stimulation takes place at room temperature and finally the region of slow OSL component. Following stimulation at ambient temperature, the relative alpha to beta response of all components was not observed to depend significantly on dose, with the value of ratio being 0.03 and a tendency to decrease with increasing dose. However, in the case of measurements performed at 125 °C, the relative response of the fast components is much enhanced, and for the remaining components it increases with increasing dose. Special care must be taken to examine the relative alpha to beta response of the fast component at 125 °C which contrasts the relative response of the TL peak at ca. 325 °C. The implications for the dating of annealed quartz are also briefly discussed.     

Mean Curvature,Threshold Dynamics,and Phase Field Theory on Finite Graphs

In the continuum, close connections exist between mean curvature flow, the Allen-Cahn (AC) partial differential equation, and the Merriman-Bence-Osher (MBO) threshold dynamics scheme. Graph analogues of these processes have recently seen a rise in popularity as relaxations of NP-complete combinatorial problems, which demands deeper theoretical underpinnings of the graph processes. The aim of this paper is to introduce these graph processes in the light of their continuum counterparts, provide some background, prove the first results connecting them, illustrate these processes with examples and identify open questions for future study. We derive a graph curvature from the graph cut function, the natural graph counterpart of total variation (perimeter). This derivation and the resulting curvature definition differ from those in earlier literature, where the continuum mean curvature is simply discretized, and bears many similarities to the continuum nonlocal curvature or nonlocal means formulation. This new graph curvature is not only relevant for graph MBO dynamics, but also appears in the variational formulation of a discrete time graph mean curvature flow. We prove estimates showing that the dynamics are trivial for both MBO and AC evolutions if the parameters (the time-step and diffuse interface scale, respectively) are sufficiently small (a phenomenon known as “freezing” or “pinning”) and also that the dynamics for MBO are nontrivial if the time step is large enough. These bounds are in terms of graph quantities such as the spectrum of the graph Laplacian and the graph curvature. Adapting a Lyapunov functional for the continuum MBO scheme to graphs, we prove that the graph MBO scheme converges to a stationary state in a finite number of iterations. Variations on this scheme have recently become popular in the literature as ways to minimize (continuum) nonlocal total variation.     

Development of a focused ultrasonic-assisted extraction of polycyclic aromatic hydrocarbons in marine sediment and mussel samples

Focused ultrasonic-assisted extraction (FUSE) is a new and particular technique based on the cavitation effect. In this work, the focused ultrasound assisted extraction was studied and developed for the extraction of polycyclic aromatic hydrocarbons from marine sediments and mussel tissues. The variables influencing the extraction (amplitude of the ultrasound pulse, the extraction time and the solvent) were studied by a full factorial design and a central composite design. As a result, flat response surfaces were obtained and the most convenient conditions were 45% of ultrasound amplitude, 120 s of extraction time and 5 mL of acetone. Both accuracy and precision of the method were evaluated by means of two certified reference materials (marine sediment and mussel tissue) and the results were also compared to those obtained by microwave assisted extraction.     

A new and efficient method for conjugate addition of trialkylphosphites to 3-acylsubstituted coumarins

A new and efficient conjugate addition of trialkylphosphites to 3-ω-bromoacetylcoumarin 1 catalysed by p-toluenesulfonic acid (TsOH) has been studied. Under the same conditions, an enolphosphate gave the corresponding esters of 3-acetyl-4-phosphono-2-oxochromans in high yields. The use of TsOH in the reaction of 3-acetyl-, 3-benzoyl-, and 3-ethoxycarbonyl coumarins led mainly to 1,4-addition products—the corresponding 3-acyl-4-dialkylphosphono-2-oxochromans—in very good yields.     

Intrinsic Fluorescence of Protoporphyrin IX from Blood Samples Can Yield Information on the Growth of Prostate Tumours

Prostate cancer is one of the most common types of cancer in men, and unfortunately many prostate tumours remain asymptomatic until they reach advanced stages. Diagnosis is typically performed through Prostate-Specific Antigen (PSA) quantification, Digital Rectal Examination (DRE) and Transrectal Ultrasonography (TU). The antigen (PSA) is secreted by all prostatic epithelial cells and not exclusively by cancerous ones, so its concentration also increases in the presence of other prostatic diseases. DRE and TU are not reliable for early detection, when histological analysis of prostate tissue obtained from a biopsy is necessary. In this context, fluorescence techniques are very important for the diagnosis of cancer. In this paper we explore the potential of using endogenous phorphyrin blood fluorescence as tumour marker for prostate cancer. Substances such as porphyrin derivatives accumulate substantially more in tumours than in normal tissues; thus, measuring blood porphyrin concentration by autofluorescence intensity may provide a good parameter for determining tumour stage. In this study, the autofluorescence of blood porphyrin was analyzed using fluorescence and excitation spectroscopy on healthy male NUDE mice and in those with prostate cancer induced by inoculation of DU145 cells. A significant contrast between the blood of normal and cancer subjects could be established. Blood porphyrin fluorophore showed an enhancement on the fluorescence band around 632 nm following tumour growth. Fluorescence detection has advantages over other light-based investigation methods: high sensitivity, high speed and safety. However it does carry the drawback of low specificity of detection. The extraction of blood porphyrin using acetone can solve this problem, since optical excitation of further molecular species can be excluded, and light scattering from blood samples is negligible.     

Analysis of reflection speckle holograms in a BSO crystal

A theoretical and experimental study of speckle registering in photorefractive BSO crystals through reflection hologram geometry is implemented. The three-dimensional speckle nature is considered in the diffraction efficiency calculations. The interference process produces index-of-refraction gratings in the speckle volume via the photorefractive effect. It is demonstrated that the coupled-wave theory for reflection geometry allows explaining the diffraction efficiency behavior when the interaction length is properly taken into account. It means that the speckle depth is related with the interaction length. The speckle depth can be controlled by the imaging system pupil aperture diameter. Under this condition, the influence of the speckle depth on the diffraction efficiency is analyzed. An agreement between the numerical model based on the coupled-wave theory and the experimental results is obtained.     

Synthesis and mass spectra of 1-arylideneamino-1,2,3-triazoles

The synthesis of the title Compounds is described. Their mass spectra upon electron impact are given and the main fragmentation pathways are described.