Sulfide formation in freshwater sediments, by sulfate-reducing microorganisms with diverse tolerance to salt

Understanding how sulfate-reducing microbes in freshwater systems respond to added salt, and therefore sulfate, is becoming increasingly important in inland systems where the threat from salinisation is increasing. To address this knowledge gap, we carried out mesocosm studies to determine how the sulfate-reducing microbial community in sediments from a freshwater wetland would respond to salinisation. The levels of inorganic mineral sulfides produced after 6 months incubation were measured to determine whether they were in sufficient quantity to be harmful if re-oxidized. Comparative sequence analysis of the dissimilatory sulfite reductase (DSR) gene was used to compare the sulfate-reducing community structure in mesocosms without salt and those incubated with moderate levels of salt. The amount of total S, acid volatile sulfide or chromium-reducible sulfide produced in sediments with 0, 1 or 5 g L^− 1 added salt were not significantly different. Sediments subjected to 15 g L^− 1 salt contained significantly higher total S and acid volatile sulfide, and levels were above trigger values for potential harm if re-oxidation occurred. The overall community structure of the sulfate-reducing microbiota (SRM) was explained by the level of salt added to sediments. However, a group of sulfate reducers were identified that occurred in both the high salt and freshwater treatments. These results demonstrate that freshwater sediments contain sulfate reducers with diverse abilities to respond to salt and can respond rapidly to increasing salinity, explaining the observation that harmful levels of acid volatile sulfides can form rapidly in sediments with no history of exposure to salt.     

Physical properties of very thin SnS films deposited by thermal evaporation

SnS films with thicknesses of 20-65 nm have been deposited on glass substrates by thermal evaporation. The physical properties of the films were investigated using X-ray diffraction (XRD), scanning electron microscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and ultraviolet-visible-near infrared spectroscopy at room temperature. The results from XRD, XPS and Raman spectroscopy analyses indicate that the deposited films mainly exhibit SnS phase, but they may contain a tiny amount of Sn₂S₃. The deposited SnS films are pinhole free, smooth and strongly adherent to the surfaces of the substrates. The color of the SnS films changes from pale yellow to brown with the increase of the film thickness from 20 nm to 65 nm. The very smooth surfaces of the thin films result in their high reflectance. The direct bandgap of the films is between 2.15 eV and 2.28 eV which is much larger than 1.3 eV of bulk SnS, this is deserving to be investigated further.     

Acidification and buffering mechanisms in acid sulfate soil wetlands of the Murray-Darling Basin, Australia

The acid generation mechanisms and neutralizing capacities of sulfidic sediments from two inland wetlands have been studied in order to understand the response of these types of systems to drying events. The two systems show vastly different responses to oxidation, with one (Bottle Bend (BB) lagoon) having virtually no acid neutralizing capacity (ANC) and the other (Psyche Bend (PB) lagoon) an ANC that is an order of magnitude greater than the acid generation potential. While BB strongly acidifies during oxidation the free acid generation is less than that expected from the measured proton production and consumption processes, with additional proton consumption attributed to the formation of an acid-anion (chloride) FeIII (oxyhydr)oxide product, similar to akagane?ite (Fe(OH)2.7Cl0.3). While such products can partially attenuate the acidification of these systems, resilience to acidification is primarily imparted by sediment ANC.     

Electrical and optical measurements on the first SCUBA-2 prototype 1280 pixel submillimeter superconducting bolometer array

SCUBA-2 is a submillimeter camera being built for the James Clerk Maxwell Telescope in Hawaii. Bringing CCD style imaging to the submillimeter for the first time, with over 10000 pixels, it will provide a revolutionary improvement in sensitivity and mapping speed. We present results of the first tests on a prototype 1280 pixel SCUBA-2 subarray; the full instrument will be made up of eight such subarrays. The array is made up of transition edge sensor (TES) detectors, with Mo/Cu bilayers as the sensing element. To keep the number of wires reasonable, a multiplexed readout is used. Unlike previous TES arrays, an in-focal plane multiplexer configuration is used, in which the multiplexing elements are located beneath each pixel. To achieve the required performance, the detectors are operated at a temperature of approximately 120 mK. We describe the results of a basic electrical and optical characterization of the array, demonstrating that it is fully operational. Noise measurements were made on several pixels and gave a noise equivalent power below 2.5 x 10(-17) W HZ(-0.5), within the requirements for SCUBA-2. The construction of the testbed used to carry out these measurements is also described.     

Salinity of animal manure and potential risk of secondary soil salinization through successive manure application

To enhance animal productivity and maximize economic returns, mineral salts are routinely added to animal feed worldwide. Salinity and ionic composition of animal manure from intensive poultry and livestock farms in Guangdong province were investigated. Field experiments were conducted for six successive crops of Brassica Parachinensis to evaluate the possibility of secondary soil salinization by successive application of chicken manure (CM) and pigeon manure (PM) to a garden soil. The concentration of total soluble salts (TSS), which were mainly composed of sulfate and chloride of potassium and sodium, averaged 49.0, 20.6 and 60.3 g.kg(- 1) in chicken, pig and pigeon manure, respectively. After three crops, successive application of CM and PM increased soil concentrations of TSS, Na(+), K(+), Mg(2+), SO(4)(2-), and Cl(-) with application rate, resulting in a rise in soil salinity from low to medium levels and a slight reduction in soil pH. After heavy rains during the last three crops, soil TSS was reduced considerably and pH showed a slight increase. Concentrations of Cl(-) and Mg(2+) increased and Ca(2+) decreased at the end of the experiment, all leading to changes in the ionic composition of soil salinity. Manure with higher ion concentrations appeared to play a more important role in affecting ionic composition of soil salinity. The results further suggest that even in a region with abundant rainfall like Guangzhou, there is still potential risk for secondary soil salinization when high rates of CM and PM are applied.     

Intermetallic phase detection in lead-free solders using synchrotron x-ray diffraction

The high-intensity, high-resolution x-ray source at the European Synchrotron Radiation Facility (ESRF) has been used in x-ray diffraction (XRD) experiments to detect intermetallic compounds (IMCs) in lead-free solder bumps. The IMCs found in 95.5Sn3.8Ag0.7Cu solder bumps on Cu pads with electroplated-nickel immersion-gold (ENIG) surface finish are consistent with results based on traditional destructive methods. Moreover, after positive identification of the IMCs from the diffraction data, spatial distribution plots over the entire bump were obtained. These spatial distributions for selected intermetallic phases display the layer thickness and confirm the locations of the IMCs. For isothermally aged solder samples, results have shown that much thicker layers of IMCs have grown from the pad interface into the bulk of the solder. Additionally, the XRD technique has also been used in a temperature-resolved mode to observe the formation of IMCs, in situ, during the solidification of the solder joint. The results demonstrate that the XRD technique is very attractive as it allows for nondestructive investigations to be performed on expensive state-of-the-art electronic components, thereby allowing new, lead-free materials to be fully characterized.     

The Transport Properties of Sodium Atoms and the Heat Capacity of Sodium Dimers at High Temperatures

Including the contribution of excited state atoms can improve calculations of dilute gaseous transport properties at high temperatures. For sodium, experimental and/or theoretical information is available about the potential energy curves associated with each of ten low-lying states of the sodium dimer. These include the ${{\rm X}^{1}\Sigma_{\rm g}{}^{+}}$ and ${^{3}\Sigma_{\rm u}{}{}^{+}}$ states that dissociate to two ground state ²S sodium atoms and the four ${^{3}\Sigma_{\rm g,u}{}^{+},\,^{1}\Sigma _{\rm g,u}{}^{+},\,^{1}\Pi _{\rm g,u},\,^{3}\Pi _{\rm g,u}}$ gerade/ungerade pairs of states that dissociate to a ground state ²S atom and an excited state ²P atom. Nine of these are bound states and have been fitted with the Hulburt–Hirschfelder potential, a very good general purpose atom–atom potential. The ³Π_g state is not bound and has been fitted with the exponential repulsive potential. We have used these potentials to calculate viscosity collision integrals as a function of temperature, and employed degeneracy-weighted averaging to determine the viscosity and translational contribution to the thermal conductivity of the sodium atoms. These same potentials have been used to calculate the heat capacity, ${C_{p}^{\rm o}}$ , of the sodium dimer using an approach that depends on the second virial coefficient and its first two temperature derivatives. Again, the inclusion of molecular states that dissociate to an excited state atom allows ${C_{p}^{\rm o}}$ to be determined with improved accuracy at higher temperatures. Thus, thermophysical property calculations for sodium have been extended to 25,000 K. These results are compared with previous results, including heat capacities given in the NIST-JANAF Thermochemical Tables.     

Determination of Intramolecular delta13C from incomplete pyrolysis fragments. Evaluation of pyrolysis-induced isotopic fractionation in fragments from the lactic acid analogue propylene glycol

Intramolecular carbon isotope ratios reflect the source of a compound and the reaction conditions prevailing during synthesis and degradation. We report here a method for determination of relative (Deltadelta13C) and absolute (delta13C) intramolecular isotope ratios using the volatile lactic acid analogue propylene glycol as a model compound, measured by on-line gas chromatography-pyrolysis coupled to GC-combustion-isotope ratio mass spectrometry. Pyrolytic fragmentation of about one-third of the analyte mass produces optimal fragments for isotopic analysis, from which relative isotope ratios (Deltadelta13C) are calculated according to guidelines presented previously. Calibration to obtain absolute isotope ratios is achieved by quantifying isotope fractionation during pyrolysis with an average fractionation factor, alpha, and evaluated by considering extremes in isotopic fractionation behavior. The method is demonstrated by calculating ranges of absolute intramolecular isotope ratios in four samples of propylene glycol. Relative and absolute isotope ratios were calculated with average precisions of SD(Deltadelta13C) <0.84 per thousand and SD(delta13C) <3.0 per thousand, respectively. The various fractionation scenarios produce an average delta(13)C range of 2 per thousand for each position in each sample. Relative isotope ratios revealed all four samples originated from unique sources, with samples A, B, and D only distinguishable at the position-specific level. Regardless of pyrolysis fractionation distribution, absolute isotope ratios showed a consistent pattern for all samples, with delta13C(3) > delta13C(2) > delta13C(1). The validity of the method was determined by examining the difference in relative isotope ratios calculated through two independent methods: Deltadelta13C calculated directly using previous methods and Deltadelta13C extracted from absolute isotope ratios. Deviation between the two Deltadelta13C values for all positions averaged 0.1-0.2 per thousand, with the smallest deviation obtained assuming equal fractionation across all fragment positions. This approach applies generally to all compounds analyzed by pyrolytic PSIA.