Luminance adaptation model for increasing the dynamic range of an imaging system based on a CCD camera

We propose a luminance adaptation model (LAM) to increase the dynamic range of an imaging system when scenes containing areas of low and high illumination are imaged. The LAM that we developed is based on capturing images at different exposure times to obtain digital levels within the linear response zone for all the pixels in the image. The levels are subsequently transformed to a reference exposure time that is common to all pixels. We use a linear transformation whose coefficients are determined by the digital levels obtained for a set of flat-spectrum samples. In this study, the LAM is applied to a multispectral imaging system that is based on a CCD camera used for color measurements and spectral reconstructions. It is shown to be a very useful method for increasing the dynamic range of the system, whilst maintaining its accuracy.     

Instabilities in optically pumped infrared lasers

The unstable emission of an optically pumped FIR gas laser is theoretically analysed through numerical resolution of the associated Maxwell-Bloch equations. The instability domain in the main control parameters space is determined and an example of chaotic behaviour is examined.     

Ion binding to polyelectrolytes: Monte Carlo simulations versus classical mean field theories

The influence of ion size and surface charge model in titrations of ionizable polyelectrolytes is studied by means of the Semi Grand Canonical Monte Carlo simulation method in the context of the primitive model. Three models describing a discrete distribution of charged functional groups on the polyelectrolyte and different values for the radius of the background electrolyte spanning from ionic to hydrated radii values were analyzed. The polyelectrolyte titrations were simulated by calculating the degree of ionization versus pH curves at two ionic strengths. The results allow us to quantify the impact of the sizes of the background salt ions and surface functional groups of the polyelectrolyte on the dissociation degree. This influence is explained in terms of the effectiveness of the screening of the charged surface sites. Finally, by comparison with the Non-Linear Poisson–Boltzmann model, the influence of ionic correlations and finite size of the solution ions is assessed.     

Nonlinear dynamics in lasing without inversion

We review lasing in homogeneously broadened coherently driven three-level systems in the framework of semiclassical density matrix formalism and using a nonlinear dynamics point of view. We discuss the following features of these systems: (i) self-pulsing lasing without inversion near the first lasing threshold, (ii) giant pulse lasing based on the population inversion without lasing phenomenon, and (iii) the enlargement of the cavity detuning range where lasing without inversion occurs by using broad-area cavities.     

Vibrational relaxation of ortho and para-H2 in the range 400-50 K

The vibrational relaxation of ortho-para-H₂ mixtures was studied in the interval 400-50 K. At and above 300 K the ortho and para self-relaxation rates, k_oo and k_pp, are identical within experimental error. In the low temperature range, k_oo >k_pp and k_oo is found to vary slowly with temperature.     

Laser irradiation of a three-level gas system: Continued-fraction theory and applications

The general steady-state solution of the density matrix equations for a Doppler broadened three-level system irradiated by two resonant standing-wave laser beams of arbritrary intensity is analyzed. The solution is expressed in a matrix continued fraction form, that involves 4×4 matrices in important configurations and is convenient for numerical computations. Some representative cases including the absorption spectra for a probe laser of arbitrary intensity, the Doppler-free multiphoton resonances and the optically pumped lasers are analyzed numerically in connection with previous experimental investigations.     

Saturation by a standing-wave laser of a Doppler-broadened three-level system: Narrow resonance due to stationary molecules

The narrow peak appearing at the center of the velocity distribution of the populations for saturation by a detuned standing-wave laser is analysed theoretically as a function of the relaxation parameters and the pump laser intensity. This peak allows high-resolution spectroscopic measurements when a frequency-unstabilized pump laser and a low intensity high-stability probe laser are used.     

Physicochemical characteristics of protein-NP bioconjugates: the role of particle curvature and solution conditions on human serum albumin conformation and fibrillogenesis inhibition

Gold nanoparticles (Au NPs) from 5 to 100 nm in size synthesized with HAuCl(4) and sodium citrate were complexed with the plasma protein human serum albumin (HSA). Size, surface charge, and surface plasmon bands of the Au NPs are largely modified by the formation of a protein corona via electrostatic interactions and hydrogen bonding as revealed by thermodynamic data. Negative values of the entropy of binding suggested a restriction in the biomolecule mobility upon adsorption. The structure of the adsorbed protein molecules is slightly affected by the interaction with the metal surface, but this effect is enhanced as the NP curvature decreases. Also, it is observed that the protein molecules adsorbed onto the NP surface are more resistant to complete thermal denaturation than free protein ones as deduced from the increases in the melting temperature of the adsorbed protein. Differences in the conformations of the adsorbed protein molecules onto small (<40 nm) and large NPs were observed on the basis of ζ-potential data and FTIR spectroscopy, also suggesting a better resistance of adsorbed protein molecules to thermal denaturing conditions. We think this enhanced protein stability is responsible for a reduced formation of HSA amyloid-like fibrils in the presence of small Au NPs under HSA fibrillation conditions.     

Aβ40 and Aβ42 amyloid fibrils exhibit distinct molecular recycling properties

A critical aspect to understanding the molecular basis of Alzheimer's disease (AD) is the characterization of the kinetics of interconversion between the different species present during amyloid-β protein (Aβ) aggregation. By monitoring hydrogen/deuterium exchange in Aβ fibrils using electrospray ionization mass spectrometry, we demonstrate that the Aβ molecules comprising the fibril continuously dissociate and reassociate, resulting in molecular recycling within the fibril population. Investigations on Aβ40 and Aβ42 amyloid fibrils reveal that molecules making up Aβ40 fibrils recycle to a much greater extent than those of Aβ42. By examining factors that could influence molecular recycling and by running simulations, we show that the rate constant for dissociation of molecules from the fibril (k(off)) is much greater for Aβ40 than that for Aβ42. Importantly, the k(off) values obtained for Aβ40 and Aβ42 reveal that recycling occurs on biologically relevant time scales. These results have implications for understanding the role of Aβ fibrils in neurotoxicity and for designing therapeutic strategies against AD.     

Supramolecular Adducts of Cucurbit[7]uril and Amino Acids in the Gas Phase

The complexation of the macrocyclic cavitand cucurbit[7]uril (Q7) with a series of amino acids (AA) with different side chains (Asp, Asn, Gln, Ser, Ala, Val, and Ile) is investigated by ESI-MS techniques. The 1:1 [Q7 + AA + 2H]²⁺ adducts are observed as the base peak when equimolar Q7:AA solutions are electrosprayed, whereas the 1:2 [Q7 + 2AA + 2H]²⁺ dications are dominant when an excess of the amino acid is used. A combination of ion mobility mass spectrometry (IM-MS) and DFT calculations of the 1:1 [Q7 + AA + 2H]²⁺ (AA = Tyr, Val, and Ser) adducts is also reported and proven to be unsuccessful at discriminating between exclusion or inclusion-type conformations in the gas phase. Collision induced dissociation (CID) revealed that the preferred dissociation pathways of the 1:1 [Q7 + AA + 2H]²⁺ dications are strongly influenced by the identity of the amino acid side chain, whereas ion molecule reactions towards N-butylmethylamine displayed a common reactivity pattern comprising AA displacement. Special emphasis is given on the differences between the gas-phase behavior of the supramolecular adducts with amino acids (AA = Asp, Asn, Gln, Ser, Ala, Val, and Ile) and those featuring basic (Lys and Arg) and aromatic (Tyr and Phe) side chains.

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