Developmental gametophyte morphology of seven species of Thelypteris subg. Cyclosorus (Thelypteridaceae)

The morphogenesis of the sexual phase of seven species of Thelypteris subg. Cyclosorus (Thelypteridaceae) is described and compared. Spores of all species are monolete, ellipsoid and have positive photoblastism. They have Vittaria-type germination, germinal filaments are short and uniseriate, and Aspidium-type development. Adult gametophytes are spatulate-cordiform, and have wide wings with numerous glandular, marginal and superficial hairs. Antheridia have a narrow or widened basal cell, an undivided annular cell, and an opercular cell; antherozoids are liberated through three mechanisms. Archegonia have short necks and four triangular cells on the neck's mouth. The sporophyte's first leaf is lobed, with open dichotomous veins, glandular hairs similar to those of the gametophyte, and anomocytic stomata. Differences observed between the studied species are: spore size; ornamentation of the perispore; germination and emergence periods; size of hairs; developmental period of gametangia; and antherozoid liberation mechanisms through total detachment of the operculum, partial detachment of the operculum, and development of an apical pore through tearing of the operculum. These taxonomically valuable characters, combined with the sporophyte characteristics, can be useful tools in the identification of the species studied to the subg. Cyclosorus.     

Chalcedony (a crystalline variety of silica): biogenic origin in electric organs from living Psammobatis extenta (family Rajidae)

The electric organs of electric fish have been used extensively for the study of peripheral cholinergic synapses. Aluminum and silicon have been observed in the electrocytes of Psammobatis extenta, a fish belonging to the family Rajidae, using a combination of scanning electron microscopy and X-ray spectrometry. Based on this evidence, the presence of silica minerals has been documented by means of mineralogical techniques. Electric organ cryostat sections and subcellular fractions were observed using a Leica DMLP mineralogical microscope. The shape, size and color, among other properties, were analyzed in plane-polarized light, while birefringence and the extinction angle, which allow for mineral identification, were observed through crossed-polarized illumination. The distribution of chalcedony, an oxide silicon mineral, in the sections and all the fractions of the electric organ was recorded. X-ray diffraction analysis of the electric organ segments showed a similar result, with a low-quartz variety. Chalcedony precipitation occurred at a specific pH (7-8) and oxidation potential (Eh; 0.0 to -0.2). This observation supports the important role played by pH and Eh conditions in silica precipitation in electrocytes, as has been reported in geological environments. It is possible that silica formation and silica degradation in electric organs are also related to the enzymes, silicatein and silicase, that direct the polymerization and depolymerization of amorphous silica in sponges. Carbonic anhydrases (silicase) are involved in physiological pH regulation. Crystallization of chalcedony via spiral growth from a partially polymerized fluid is consistent with processes known to occur in organic systems. This is the first time that a biogenically produced crystalline mineral phase (i.e., chalcedony) has been observed in the electrocytes and cholinergic nerves from living electric fish.     

Radio-frequency association of molecules: an assisted Feshbach resonance

We develop a theoretical model to describe the radio-frequency (rf) induced coupling of a pair of colliding atoms to a Feshbach molecule when a magnetic field arbitrarily far from the Feshbach resonance is modulated in time. We use the dressed atom picture, and show that the coupling strength in presence of rf is equal to the Feshbach coupling strength multiplied by the square of a Bessel function. The argument of this function is equal to the ratio of the atomic rf Rabi frequency to the rf frequency. We experimentally demonstrate this law by measuring the rate of rf-association of molecules using a Feshbach resonance in d wave collisions between ultra-cold chromium atoms.     

Photodegradation of butyl acrylate in the troposphere by OH radicals: kinetics and fate of 1,2‐hydroxyalcoxy radicals

The rate constant of the reaction of OH radicals with butyl acrylate was studied for the first time using an atmospheric simulation chamber at 298 K and ～750 Torr of air or nitrogen. The decay of the organics was followed using a gas chromatograph with a flame ionization detector (GC‐FID), and the rate constant was determined using a relative rate method with different references. The obtained average value of (1.80 ± 0.26) × 10^?11 cm³ molecule^?1 s^?1 is in agreement with previous determinations of the rate constants of OH radicals with acrylates and methacrylates in the literature. Additionally, product identification under atmospheric conditions was performed for the first time by the GC‐MS technique. Butyl glyoxalate was observed as the degradation product in accordance with the addition of OH to the less substituted carbon atom of the double bond, followed by decomposition of the 1,2‐hydroxyalkoxy radicals formed. Room temperature rate coefficient was used to estimate the atmospheric lifetime of the ester studied. Reactivity trends are discussed in terms of the substituent effects and the length of the hydrogenated chain of the ester. The atmospheric persistence of BUAC was calculated taking into account the experimental rate constant obtained. Copyright © 2008 John Wiley & Sons, Ltd.     

Experimental and kinetic modeling study of oxidation of acetonitrile

Oxidation of acetonitrile has been studied in a flow reactor in the absence and presence of nitric oxide. The experiments were conducted at atmospheric pressure in the temperature range 1150–1450 K, varying the excess air ratio from slightly fuel-lean to very lean. Oxidation of CH₃CN was slow below 1300 K. Nitric oxide, hydrogen cyanide and nitrous oxide were detected as important products. A detailed chemical kinetic model for oxidation of acetonitrile was developed, based on a critical evaluation of data from literature. The rate coefficients for the reactions of CH₃CN and CH₂CN with O₂ were calculated from ab initio theory. Modeling predictions were in satisfactory agreement with experiments. Calculations were sensitive to thermal dissociation of CH₃CN and to the branching fraction for CH₃CN + OH to CH₂CN + H₂O and HOCN + CH₃, respectively. More work is desirable for these steps, as well as for reactions of CH₂CN and HCCN.     

Optical properties of thin Cu<Subscript>2</Subscript>ZnSnS<Subscript>4</Subscript>, films produced by RF magnetron sputtering

Optical properties of thin Cu₂ZnSnS₄ films produced by RF magnetron sputtering of preliminarily synthesized material are studied. Transmission and reflection coefficients are studied in a range from 0.4 to 26 μm. The optical band-gap width depending on substrate temperature is estimated; in optimal modes, it is equal to 1.47 eV. The study of electrical properties shows that Cu₂ZnSnS₄ possesses low charge-carrier mobility, μ = 1.9 cm²/(V s), at room temperature and hole concentration р = 5 × 10¹⁸ cm^–3. Electron microscopy shows that the film possesses a polycrystalline structure with a crystallite size on the order of 100 nm.     

Using permutations to detect dependence between time series

In this paper, we propose an independence test between two time series which is based on permutations. The proposed test can be carried out by means of different common statistics such as Pearson’s chi-square or the likelihood ratio. We also point out why an exact test is necessary. Simulated and real data (return exchange rates between several currencies) reveal the capacity of this test to detect linear and nonlinear dependences.     

Temperature dependence of the Ho L2‐edge XMCD spectra of Ho6Fe23

An X‐ray magnetic circular dichroism (XMCD) study performed at the Ho L_2,3‐edges in Ho₆Fe₂₃ as a function of temperature is presented. It is demonstrated that the anomalous temperature dependence of the Ho L₂‐edge XMCD signal is due to the magnetic contribution of Fe atoms. By contrast, the Ho L₃‐edge XMCD directly reflects the temperature dependence of the Ho magnetic moment. By combining the XMCD at both Ho L₂‐ and L₃‐edges, the possibility of determining the temperature dependence of the Fe magnetic moment is demonstrated. Then, both μ_Ho(T) and μ_Fe(T) have been determined by tuning only the absorption L‐edges of Ho. This result opens new possibilities of applying XMCD at these absorption edges to obtain quantitative element‐specific magnetic information that is not directly obtained by other experimental tools.