932 research outputs found
Современные тенденции развития рекреационного хозяйства в Украине
Chromiferous ultramafic rocks from Campo Formoso (Bahia State, Brazil) exhibit various stages of hydrothermal alteration and weathering, each being characterized by distinct chromiferous parageneses. These Cr-bearing minerals are mainly phyllosilicates, but other phases are also present as chromiferous opal and hydroxycarbonates. Optical absorption spectra and K-edge fine structure allow a better knowledge of chromium crystal chemistry in these minerals. The first stages of chromite oxidation have been precised, and particularly the influence of structural factors was pointed out : the inversion grade of these spinels controls the evolution from a mainly direct chromite to the inverse forms (ferritchromit). Chromium ions inserted in mineral structures do not exhibit any change in the oxidation state during alteration processes. In contrast, crystal field stabilization energy (CFSE) of Cr3+ ions exhibits important variations among the studied minerals. Study of EXAFS spectra demonstrated that Cr-O distances do not change significandy among the investigated minerals, the effective oxygen charge playing the main role in the observed CFSE variations. This latter parameter explains the concentration of chromium in these minerals and contributes to the stability of some phases like clinochlores and hydroxycarbonates, where trivalent chromium has the highest CFSE.Les ultrabasites chromifères de Campo Formoso (Etat de Bahia, Brésil) montrent plusieurs stades successifs d'altération hydrothermale puis superficielle qui s'accompagnent de paragenèses chromifères variées. Les minéraux caractéristiques de ces dernières sont essentiellement des phyllosilicates, mais on note aussi d'autres phases comme la stichtite et l'opale chromifère. Les spectres d'absorption X ont permis de caractériser la cristallochimie du chrome dans ces minéraux. Les premiers stades d'oxydation des chromites ont été précisés, en particulier l'influence de la structure réelle du spinelle (degré d'inversion) qui contrôle les conditions d'évolution de la chromite. Le degré d'oxydation +3 du chrome est conservé lors des processus d'altération et seule l'énergie de stabilisation liée au champ cristallin montre des changements importants. L'étude des spectres EXAFS (Extended X-ray Absorption Fine Structure) a montré que, les distances Cr-O ne changeant pas entre les minéraux étudiés, seule la nature des ligandes a une influence sur la valeur de l'énergie de champ cristallin. Ceci explique la forte concentration en chrome de ces minéraux d'altération et contribue à la stabilité des phases comme les clinochlores ou les hydroxycarbonates où les ions Cr3+ ont la plus forte énergie de stabilisation.Calas Georges, Manceau Alain, Novikoff André, Boukili Hassan. Comportement du chrome dans les minéraux d'altération du gisement de chromite de Campo Formoso (Bahia, Brésil). In: Bulletin de Minéralogie, volume 107, 6, 1984. pp. 755-766
Localization and speciation of Zn in mycorrihizd roots by μSXRF and μEXAFS.
Mycorrhizae are symbiotic associations between soil fungi and plant roots, which enhance mineral nutrition for the plant, and might play an important role in metals acquisition and accumulation. The processes allowing metals mobilization in the soil, absorption by the root and/or the fungus, transfer or bioaccumulation are still poorly understood. However, the properties of mycorrhizal fungi could be used for phytoremediation, a soft technique using plants for the clean-up of metal polluted soils. In this work, mycorrhized roots of tomato plants grown in a Zn-contaminated soil were investigated. The distribution of metals and the speciation of Zn were studied at the micron scale using micro synchrotron-based X-ray fluorescence (μSXRF) and micro X-ray absorption spectroscopy (μEXAFS). Zn associated to the root was Zn malate and/or Zn citrate, and Zn associated to the fungus was Zn phyllosilicate. This study illustrates the great potential of X-ray microbeams for the study of biological samples containing various amounts of metals
RPANDA: an R package for macroevolutionary analyses on phylogenetic trees
A number of approaches for studying macroevolution using phylogenetic trees have been developed in the last few years. Here, we present RPANDA, an R package that implements model‐free and model‐based phylogenetic comparative methods for macroevolutionary analyses. The model‐free approaches implemented in RPANDA are recently developed approaches stemming from graph theory that allow summarizing the information contained in phylogenetic trees, computing distances between trees, and clustering them accordingly. They also allow identifying distinct branching patterns within single trees. RPANDA also implements likelihood‐based models for fitting various diversification models to phylogenetic trees. It includes birth–death models with i) constant, ii) time‐dependent and iii) environmental‐dependent speciation and extinction rates. It also includes models with equilibrium diversity derived from the coalescent process, as well as a likelihood‐based inference framework to fit the individual‐based model of Speciation by Genetic Differentiation, which is an extension of Hubbell's neutral theory of biodiversity. RPANDA can be used to (i) characterize trees by plotting their spectral density profiles (ii) compare trees and cluster them according to their similarities, (iii) identify and plot distinct branching patterns within trees, (iv) compare the fit of alternative diversification models to phylogenetic trees, (v) estimate rates of speciation and extinction, (vi) estimate and plot how these rates have varied with time and environmental variables and (vii) deduce and plot estimates of species richness through geological time. RPANDA provides investigators with a set of tools for exploring patterns in phylogenetic trees and fitting various models to these trees, thereby contributing to the ongoing development of phylogenetics in the life sciences
Pseudomonas cannabina pv. cannabina pv. nov., and Pseudomonas cannabina pv. alisalensis (Cintas Koike and Bull, 2000) comb. nov., are members of the emended species Pseudomonas cannabina (ex Šutič & Dowson 1959) Gardan, Shafik, Belouin, Brosch, Grimont
Sequence similarity in the 16S rDNA gene confirmed that crucifer pathogen Pseudomonas syringae pv. alisalensis belongs to P. syringae sensu lato. In reciprocal DNA/DNA hybridization experiments, DNA relatedness was high (69–100%) between P. syringae pv. alisalensis strains and the type strain of P. cannabina (genomospecies 9). In contrast, DNA relatedness was low (below 48%) between P. syringae pv. alisalensis and reference strains from the remaining genomospecies of P. syringae including the type strain of P. syringae and reference strain of genomospecies 3 (P. syringae pv. tomato) although the well-known crucifer pathogen, P. syringae pv. maculicola, also belongs to genomospecies 3. Additional evidence that P. syringae pv. alisalensis belongs to P. cannabina was sequence similarity in five gene fragments used in multilocus sequence typing, as well as similar rep-PCR patterns when using the BOX-A1R primers. The description of P. cannabina has been emended to include P. syringae pv. alisalensis. Host range testing demonstrated that P. syringae pv. alisalensis strains, originally isolated from broccoli, broccoli raab or arugula, were not pathogenic on Cannabis sativa (family Cannabinaceae). Additionally, P. cannabina strains, originally isolated from the C. sativa were not pathogenic on broccoli raab or oat while P. syringae pv. alisalensis strains were pathogenic on these hosts. Distinct host ranges for these two groups indicate that P. cannabina emend. consists of at least two distinct pathovars, P. cannabina pv. cannabina pv. nov., and P. cannabina pv. alisalensis comb. nov. Pseudomonas syringae pv. maculicola strain CFBP 1637 is a member of P. cannabina
Theory of coherent optical nonlinearities of intersubband transitions in semiconductor quantum wells
We theoretically study the coherent nonlinear response of electrons confined
in semiconductor quantum wells under the effect of an electromagnetic radiation
close to resonance with an intersubband transition. Our approach is based on
the time-dependent Schr\"odinger-Poisson equation stemming from a Hartree
description of Coulomb-interacting electrons. This equation is solved by
standard numerical tools and the results are interpreted in terms of
approximated analytical formulas. For growing intensity, we observe a redshift
of the effective resonance frequency due to the reduction of the electric
dipole moment and the corresponding suppression of the depolarization shift.
The competition between coherent nonlinearities and incoherent saturation
effects is discussed. The strength of the resulting optical nonlinearity is
estimated across different frequency ranges from mid-IR to THz with an eye to
ongoing experiments on Bose-Einstein condensation of intersubband polaritons
and to the speculative exploration of quantum optical phenomena such as
single-photon emission in the mid-IR and THz windows
Demonstration and frequency noise characterization of a 17 m quantum cascade laser
We describe the properties of a continuous-wave room-temperature quantum
cascade laser operating at the long wavelength of 17 m. Long wavelength
mid-infrared quantum cascade lasers offer new opportunities for chemical
detection, vibrational spectroscopy and metrological measurements using
molecular species. In particular, probing low energy vibrational transitions
would be beneficial to the spectroscopy of large and complex molecules,
reducing intramolecular vibrational energy redistribution which acts as a
decoherence channel. By performing linear absorption spectroscopy of the v2
fundamental vibrational mode of N2O molecules, we have demonstrated the
spectral range and spectroscopic potential of this laser, and characterized its
free-running frequency noise properties. Finally, we also discuss the potential
application of this specific laser in an experiment to test fundamental physics
with ultra-cold molecules
Room temperature strong light-matter coupling in three dimensional terahertz meta-atoms
We demonstrate strong light-matter coupling in three dimensional terahertz meta-atoms at room temperature. The intersubband transition of semiconductor quantum wells with a parabolic energy potential is strongly coupled to the confined circuital mode of three-dimensional split-ring metal-semiconductor-metal resonators that have an extreme sub-wavelength volume (λ/10). The frequency of these lumped-element resonators is controlled by the size and shape of the external antenna, while the interaction volume remains constant. This allows the resonance frequency to be swept across the intersubband transition and the anti-crossing characteristic of the strong light-matter coupling regime to be observed. The Rabi splitting, which is twice the Rabi frequency (2ΩRabi), amounts to 20% of the bare transition at room temperature, and it increases to 28% at low-temperatur
Coupled-cavity terahertz quantum cascade lasers for single mode operation
We demonstrate the operation of coupled-cavity terahertz frequency quantum-cascade lasers composed of two sub-cavities separated by an air gap realized by optical lithography and dry etching. This geometry allows stable, single mode operation with typical side mode suppression ratios in the 30-40 dB range. We employ a transfer matrix method to model the mode selection mechanism. The obtained results are in good agreement with the measurements and allow prediction of the operating frequency
Optically Implemented Broadband Blueshift Switch in the Terahertz Regime
Cataloged from PDF version of article.We experimentally demonstrate, for the first time, an optically implemented blueshift tunable metamaterial in the terahertz (THz) regime. The design implies two potential resonance states, and the photoconductive semiconductor (silicon) settled in the critical region plays the role of intermediary for switching the resonator from mode 1 to mode 2. The observed tuning range of the fabricated device is as high as 26% (from 0.76 THz to 0.96 THz) through optical control to silicon. The realization of broadband blueshift tunable metamaterial offers opportunities for achieving switchable metamaterials with simultaneous redshift and blueshift tunability and cascade tunable devices. Our experimental approach is compatible with semiconductor technologies and can be used for other applications in the THz regime
Near-to mid-IR spectral purity transfer with a tunable frequency comb: methanol frequency metrology over a record frequency span
We report the development and operation of a frequency-comb-assisted
high-resolution mid-infrared molecular spectrometer combining high spectral
purity, SI-traceability, wide tunability and high sensitivity. An optical
frequency comb is used to transfer the spectral purity of a SI-traceable 1.54
m metrology-grade frequency reference to a 10.3 m quantum cascade
laser (QCL). The near-infrared reference is operated at the French
time/frequency metrology institute, calibrated there to primary frequency
standards, and transferred to Laboratoire de Physique des Lasers via the
REFIMEVE fiber network. The QCL exhibits a sub-10 --15 frequency stability from
0.1 to 10 s and its frequency is traceable to the SI with a total uncertainty
better than 4 x 10 --14 after 1-s averaging time. We have developed the
instrumentation allowing comb modes to be continuously tuned over 9 GHz
resulting in a QCL of record spectral purity uninterruptedly tunable at the
precision of the reference over an unprecedented span of 1.4 GHz. We have used
our apparatus to conduct sub-Doppler spectroscopy of methanol in a multi-pass
cell, demonstrating state-of-art frequency uncertainties down to the few
kilohertz level. We have observed weak intensity resonances unreported so far,
resolved subtle doublets never seen before and brought to light discrepancies
with the HITRAN database. This demonstrates the potential of our apparatus for
probing subtle internal molecular processes, building accurate spectroscopic
models of polyatomic molecules of atmospheric or astrophysical interest, and
carrying out precise spectroscopic tests of fundamental physics
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