Galactic Phylogenetics

Phylogenetics is a widely used concept in evolutionary biology. It is the reconstruction of evolutionary history by building trees that represent branching patterns and sequences. These trees represent shared history, and it is our intention for this approach to be employed in the analysis of Galactic history. In Galactic archaeology the shared environment is the interstellar medium in which stars form and provides the basis for tree-building as a methodological tool. Using elemental abundances of solar-type stars as a proxy for DNA, we built in Jofre et al 2017 such an evolutionary tree to study the chemical evolution of the solar neighbourhood. In this proceeding we summarise these results and discuss future prospects.Comment: Contribution to IAU Symposium No. 334: Rediscovering our Galax

Electrical reduction of perovskite electrodes for accelerating exsolution of nanoparticles

This work was supported through the Leading Graduate School Program: Academy for Co-creative Education of Environment and Energy Science (ACEEES) funded by the Ministry of Education, Culture, Sports, Science and Technology (MEXT, Japan).Growth of finely dispersed nanocatalysts by exsolution of metal nanoparticles from perovskite oxides under reducing conditions at elevated temperature is a promising approach of producing highly active catalytic materials. An alternative method of exsolution using an applied potential has been recently shown to potentially accelerate the exsolution process of nanoparticles that can be achieved in minutes rather than the hours required in chemical reduction. In the present study, we investigate exsolution of nanoparticles from perovskite oxides of La0.43Ca0.37Ni0.06Ti0.94O3-γ (LCTNi) and La0.43Ca0.37Ni0.03Fe0.03Ti0.94O3-γ (LCTNi-Fe) under applied potentials in carbon dioxide atmosphere. The impedance spectra of single cells measured before and after electrochemical poling at varying voltages showed that the onset of exsolution process occurred at 2 V of potential reduction. An average particle size of the exsolved nanoparticles observed after testing using a scanning electron microscopy was about 30–100 nm. The cells with the reduced electrodes exhibited desirable electrochemical performances not only in pure carbon dioxide (current density of 0.37 A cm−2 for LCTNi and 0.48 A cm−2 for LCTNi-Fe at 1.5 V) but also in dry hydrogen (0.36 W cm−2 for LCTNi and 0.43 W cm−2 for LCTNi-Fe).PostprintPeer reviewe

Characterisation of microplastics is key for reliable data interpretation.

Microplastic research has gained attention due to the increased detection of microplastics (<5 mm size) in the aquatic environment. Most laboratory-based research of microplastics is performed using microparticles from specific suppliers with either superficial or no characterisation performed to confirm the physico-chemical information detailed by the supplier. The current study has selected 21 published adsorption studies to evaluate how the microplastics were characterised by the authors' prior experimentation. Additionally, six microplastic types described as "small" (10–25 μm) and "large" (100 μm) were commercially acquired from a single supplier. A detailed characterisation was performed using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction, differential scanning calorimetry, scanning electron microscopy, particle size analysis, and N2-Brunauer, Emmett and Teller adsorption-desorption surface area analysis. The size and the polymer composition of some of the material provided by the supplier was inconsistent with the analytical data obtained. FT-IR spectra of small polypropylene particles indicated either oxidation of the particles or the presence of a grafting agent which was absent in the large particles. A wide range of sizes for the small particles was observed: polyethylene (0.2–549 μm), polyethylene terephthalate (7–91 μm) and polystyrene (1–79 μm). Small polyamide (D50 75 μm) showed a greater median particle size and similar size distribution when compared to large polyamide (D50 65 μm). Moreover, small polyamide was found to be semi-crystalline, while the large polyamide displayed an amorphous form. The type of microplastic and the size of the particles are a key factor in determining the adsorption of pollutants and subsequent ingestion by aquatic organisms. Acquiring uniform particle sizes is challenging, however based on this study, characterisation of any materials used in microplastic-related experiments is critical to ensure reliable interpretation of results, thereby providing a better understanding of the potential environmental consequences of the presence of microplastics in aquatic ecosystems

Complete Genome and Transcriptomes of Streptococcus parasanguinis FW213: Phylogenic Relations and Potential Virulence Mechanisms

Streptococcus parasanguinis, a primary colonizer of the tooth surface, is also an opportunistic pathogen for subacute endocarditis. The complete genome of strain FW213 was determined using the traditional shotgun sequencing approach and further refined by the transcriptomes of cells in early exponential and early stationary growth phases in this study. The transcriptomes also discovered 10 transcripts encoding known hypothetical proteins, one pseudogene, five transcripts matched to the Rfam and additional 87 putative small RNAs within the intergenic regions defined by the GLIMMER analysis. The genome contains five acquired genomic islands (GIs) encoding proteins which potentially contribute to the overall pathogenic capacity and fitness of this microbe. The differential expression of the GIs and various open reading frames outside the GIs at the two growth phases suggested that FW213 possess a range of mechanisms to avoid host immune clearance, to colonize host tissues, to survive within oral biofilms and to overcome various environmental insults. Furthermore, the comparative genome analysis of five S. parasanguinis strains indicates that albeit S. parasanguinis strains are highly conserved, variations in the genome content exist. These variations may reflect differences in pathogenic potential between the strains

Solar-driven semi-conductor photocatalytic water treatment (TiO2, g-C3N4, and TiO2+g-C3N4) of cyanotoxins: proof-of-concept study with microcystin-LR.

Cyanobacteria and their toxins are a threat to drinking water safety as increasingly cyanobacterial blooms (mass occurrences) occur in lakes and reservoirs all over the world. Photocatalytic removal of cyanotoxins by solar light active catalysts is a promising way to purify water at relatively low cost compared to modifying existing infrastructure. We have established a facile and low-cost method to obtain TiO2 and g-C3N4 coated floating photocatalysts using recycled glass beads. g-C3N4 coated and TiO2+g-C3N4 co-coated beads were able to completely remove microcystin-LR in artificial fresh water under both natural and simulated solar light irradiation without agitation in less than 2 h. TiO2 coated beads achieved complete removal within 8 h of irradiation. TiO2+g-C3N4 beads were more effective than g-C3N4 beads as demonstrated by the increase reaction rate with reaction constants, 0.0485 min−1 compared to 0.0264 min−1 respectively, with TiO2 alone found to be considerably slower 0.0072 min−1. g-C3N4 based photocatalysts showed a similar degradation pathway to TiO2 based photocatalysts by attacking the C6–C7 double bond on the Adda side chain

Aging microplastics enhances the adsorption of pharmaceuticals in freshwater.

Plastic pollution is an increasing environmental concern. Pollutants such as microplastics (< 5 mm) and pharmaceuticals often co-exist in the aquatic environment. The current study aimed to elucidate the interaction of pharmaceuticals with microplastics and ascertain how the process of photo-oxidation of microplastics affected the adsorption of the pharmaceuticals. To this end, a mixture containing ibuprofen, carbamazepine, fluoxetine, venlafaxine and ofloxacin (16 μmol L−1 each) was placed in contact with one of six either virgin or aged microplastic types. The virgin microplastics were acquired commercially and artificially aged in the laboratory. Polypropylene, polyethylene, polyethylene terephthalate, polyamide, polystyrene and polyvinyl chloride microparticles were evaluated at two sizes, described as small (D50 < 35 μm) and large (D50 95–157 μm). Results demonstrated that the study of virgin particles may underestimate the adsorption of micropollutants onto microplastics. For virgin particles, only small microparticles of polypropylene, polyethylene, polyvinyl chloride and both sizes of polyamide adsorbed pharmaceuticals. Aging the microplastics significantly increased the adsorption of pharmaceuticals by microplastics. Fluoxetine adsorbed onto all aged microplastics, from 18% (large polyethylene terephthalate) to 99% (small polypropylene). The current investigation highlights the potential of microplastics to act as a vector for pharmaceuticals in freshwater, especially after aging

Adsorption of cyanotoxins on polypropylene and polyethylene terephthalate: microplastics as vector of eight microcystin analogues.

Plastics are utilised globally but are of environmental concern due to their persistence. The global presence of microplastics (particles <5 mm in all dimensions) in freshwater environments is increasingly reported, as has the presence of cyanobacterial toxins, including the microcystins. We elucidated the potential role of microplastics as a vector for eight microcystin analogues. Two sizes of polypropylene (PP) and polyethylene terephthalate (PET) microparticles were evaluated. The median particle size distribution (D50) was 8–28 μm for small particles, and 81–124 μm for large particles. Additionally, microcystin-LR and -LF were evaluated individually using small PP and PET to elucidate the adsorption behaviour in the absence of competition. Microcystin hydrophobicity, polymer material, and particle size were key factors influencing adsorption to the plastic microparticles. The small size PP microparticles demonstrated a high affinity for the 8 microcystin analogues. The proportion of microcystin adsorbed onto the small particles of PP after 48 h contact was between 83 and 100%, depending on the analogue. Of all analogues investigated, only microcystin-LW and -LF adsorbed onto the larger sized PP and PET microparticles. Individually, greater amounts of MC-LF adsorbed onto the small PET (19%) compared to when it was present in the mixture of microcystins (11%). While MC-LR did not adsorb onto small PET microparticles in the mixture, 5% adsorption was observed when individually in contact with small PET microparticles. The results demonstrated that microplastics can adsorb eight different microcystin analogues and that more hydrophobic analogues are more likely to adsorb than less hydrophobic analogues

A novel in situ diffusion strategy to fabricate high performance cathodes for low temperature proton-conducting solid oxide fuel cells

This work was supported by the National Natural Science Foundation of China (Grant No.: 21676261, U1632131 and 51602238). The authors acknowledge the financial support of the Royal Society of Edinburgh for a RSE BP Hutton Prize in Energy Innovation and EPSRC Platform grant, EP/K015540/1. We also would like to thank the support from the China Scholarship Council (No. 201606340101).Developing new low-cost high-performance cobalt-free cathode materials for low temperature proton-conducting solid oxide fuel cells (H-SOFCs) has been an imperative topic. In response to this challenge, we herein develop a novel in situ Pr diffusion strategy based on a Sm0.2Ce0.8O2-δ-Pr(Pr0.5Ba1.5)Cu3O7-δ (SDC-PBCu, 3:7 wt%) compound, to achieve a perovskite-related proton-blocking composite cathode (PBCC) Ce1-xPrxO2-δ-Ba2CeCu3O7.4-Sm2Ba1.33Ce0.67Cu3O9-CuO (PDC-BCC-SBCC-CuO) for BaZr0.1Ce0.7Y0.2O3-δ-based H-SOFCs. The single cell achieves a remarkable performance with a maximum power density (MPD) of 1000 and 566 mW cm-2, corresponding to the interfacial polarization resistance (RP) of 0.037 and 0.188 Ω cm2 at 700 and 600 °C, respectively. The XRD results demonstrate that the PBCu phase disappears after the calcination of the mixed SDC-PBCu composite powder at 900 °C, with the formation of four new phases including fluorite structured PDC, orthorhombic layered material BCC, tetragonal perovskite-related SBCC and a small quantity of metallic oxide CuO, being favorable for a superior cathode performance. The ascendant electrochemical performance including the very high MPD and the lower RP obtained here indicate that the quaternary cobalt-free PBCC PDC-BCC-SBCC-CuO is a preferable alternative for high-performance low-temperature H-SOFCs.PostprintPostprintPeer reviewe

Evolution of Anodic Product from Molybdenum Metal in Absolute Ethanol and Humidity Sensing under Ambient Conditions

Authors would like to thank the support from National Natural Science Foundation of China (NSFC) (Nos. 51702264 and 41371275), Fundamental Research Funds for the Central Universities (No. XDJK2017B033), and Research Funding of Southwest University (No. SWU117019). The funding from the Engineering and Physical Sciences Research Council (EPSRC) (under Grant Nos. EP/K022237/1, EP/K036769/1, and EP/M024938/1) is also acknowledged. We also appreciate the funding from the EU COST Action (No. TD1208) for useful exchanges and discussions.Room-temperature nonaqueous synthetic routes turn out to be particularly competitive among all the available liquid-phase synthetic methods for nanometer-sized metal oxides for multiple applications. Microplasma-assisted anodization is employed to prepare soluble and crystalline Mo species in a water-deficient and extraneous ionic-salt-free ethanol electrolyte. The anodization of Mo in absolute ethanol is found to produce Mo oxyethoxide in the liquid ethanol phase, along with a small montage of mixed hexagonal and orthorhombic MoO3 crystals. The evolution of Mo species in solid and liquid phases is characterized to study the crystallization of MoO3 crystal and the formation of blue spherical Mo polyoxometalates (POMs) after extended aging. The addition of water in the suspension delayed the formation of molybdenum blue while hydrogen peroxide induced the precipitation of a dendritic framework of hexagonal MoO3. A thin MoO3 film was produced from the solution and can be used for humidity sensing by the facile conductivity measurement.PostprintPostprintPeer reviewe