Structure-property relations of highly ordered bio-nanocomposites

Bio-nanocomposites with superior mechanical, transport and flame-retardant properties can be produced from the combination of biopolymers and silicate nanoclay platelets, such as montmorillonite (MMT) [1,2,4]. The highly ordered nanostructure observed in such systems is often compared to natural ones, such as in the brick-and-mortar arrangement of aragonite plates in nacreous materials [3]. Previous work on nacre-mimetic alginate/MMT nanocomposites has shown good compatibility between the biopolymer and inorganic filler and a dependence on MMT concentration to the level of alignment [4]. In this study, we investigate the effect of gelation on the orientation of nanoparticles and its impact on clay stacking and effective aspect ratio. Thermo-reversible gelling biopolymers, i.e. gelatin and carrageenan, were used as matrices to induce early gelation; and compared to sodium alginate (late gelling reaction). Self-supporting bio-nanocomposite films based on gelatin or carrageenan, with a wide range of Na-montmorillonite concentration – up to 80 wt.% MMT – were successfully prepared by solvent casting. The obtained films display a highly aligned nacre-like structure (Fig. 1). To investigate the effect of MMT ordering on the mechanical properties, we have analyzed the obtained films with dynamic mechanical thermal analysis. The bio-nanocomposite films display exceptional mechanical properties, with storage modulus as high as 33 GPa (carrageenan/MMT); and high reinforcement depending on MMT concentration (Fig. 2). At remarkably high inorganic fraction, 80 wt.% MMT, early gelling biopolymers showed a continued increase in material reinforcement, whereas late gelation shows a slight decrease. This suggests that early gelling might reduce restacking of MMT platelets, thus, improving the effective aspect ratio of the filler. The highly ordered structure observed in the gelatin 80 wt.% MMT composite was also reflected in its high heat distortion temperature, implying lower oxygen diffusivity. To better understand the influence of gelation and MMT addition on the mechanical properties, we further applied a conventional composite theory (Halpin-Tsai model), which considers the individual contributions of filler, such as the level of alignment, aspect ratio, volume fraction, and the modulus of the MMT platelets. Please click Additional Files below to see the full abstract

Standard negation: the curious case of South America

This study compares standard negation in the indigenous languages of South America to the rest of the world. We show that South American languages not only prefer postverbal negation to preverbal negation and negative morphology to syntax, but postverbal morphological negation to any other negation strategy. The predominance of this strategy makes South America distinct from other macro-areas. The study also considers the areal distribution of negation on the South American continent. It shows that negation strategies each have their own concentration area. Postverbal morphological negation, which is the dominant strategy, turns out to be concentrated in the northwest of the continent, with the highest density around the boundaries between Colombia, Peru and Brazil. We suggest that the preference for postverbal morphological negation in South America is likely to be the result of language-internal mechanisms of negation renewal, coupled with language contact.Horizon 2020(H2020)Marie Skłodowska-Curie grant No 895548Descriptive and Comparative Linguistic

Modelling sea level driven change of Macaronesian archipelago configurations since 120 kyr BP

The MacArthur and Wilson island biogeography theory relates species diversity on islands as the result of equilibrium between extinctions and colonization events which rates depend on island size and isolation. Although island size and isolation can be considered static on ecological timescales (<100 years) they are not static on longer time scales. Since the last million years sea levels fluctuate with a period of ca. 120 kyr between -120 m and up to +10 m MSL (Mean Sea Level). Due to these sea level changes islands have changed in size and ultimately may have drowned or emerged. The rate and degree of their drowning depends on island morphometry and the shape of the sea level change curve. We explore the effects of global sea level cycles on the configuration of archipelagos and volcanic islands of Macaronesia. The results indicate that the islands changed shape considerably during the last 120 kyr. Notably the period between 80 kyr and 15 kyr ago sea levels were at least 80 m lower than present and several islands now isolated were merged or were much larger than present. Recent shrinking of islands due to the sea level rise since the last glacial maximum period (20 kyr BP) led to more than 50% reductions in island size, significant loss of coastal habitat and a significant increase in isolation by the increase of distances between islands and island and continents. Island size reduction must have induced pressures especially on terrestrial insular ecosystems, inducing upward migrations and interspecies competitions, and probable extinctions. The splitting of merged islands must have led to separations of populations leading to gene flow losses for some biota. Present day islands are not representative for the mean island configurations during the last Myr but rather represent an anomaly. Islands at present are smallest and most isolated and this configuration makes the insular biota even more vulnerable to human impact

Global raster dataset on historical coastline positions and shelf sea extents since the Last Glacial Maximum

Motivation: Historical changes in sea level caused shifting coastlines that affected the distribution and evolution of marine and terrestrial biota. At the onset of the Last Glacial Maximum (LGM) 26 ka, sea levels were >130 m lower than at present, resulting in seaward-shifted coastlines and shallow shelf seas, with emerging land bridges leading to the isolation of marine biota and the connection of land-bridge islands to the continents. At the end of the last ice age, sea levels started to rise at unprecedented rates, leading to coastal retreat, drowning of land bridges and contraction of island areas. Although a growing number of studies take historical coastline dynamics into consideration, they are mostly based on past global sea-level stands and present-day water depths and neglect the influence of global geophysical changes on historical coastline positions. Here, we present a novel geophysically corrected global historical coastline position raster for the period from 26 ka to the present. This coastline raster allows, for the first time, calculation of global and regional coastline retreat rates and land loss rates. Additionally, we produced, per time step, 53 shelf sea rasters to present shelf sea positions and to calculate the shelf sea expansion rates. These metrics are essential to assess the role of isolation and connectivity in shaping marine and insular biodiversity patterns and evolutionary signatures within species and species assemblages. Main types of variables contained: The coastline age raster contains cells with ages in thousands of years before present (bp), representing the time since the coastline was positioned in the raster cells, for the period between 26 ka and the present. A total of 53 shelf sea rasters (sea levels <140 m) are presented, showing the extent of land (1), shelf sea (0) and deep sea (NULL) per time step of 0.5 kyr from 26 ka to the present. Spatial location and grain: The coastline age raster and shelf sea rasters have a global representation. The spatial resolution is scaled to 120 arcsec (0.333° × 0.333°), implying cells of c. 3,704 m around the equator, 3,207 m around the tropics (±30°) and 1,853 m in the temperate zone (±60°). Time period and temporal resolution: The coastline age raster shows the age of coastline positions since the onset of the LGM 26 ka, with time steps of 0.5 kyr. The 53 shelf sea rasters show, for each time step of 0.5 kyr, the position of the shelf seas (seas shallower than 140 m) and the extent of land. Level of measurement: Both the coastline age raster and the 53 shelf sea rasters are provided as TIFF files with spatial reference system WGS84 (SRID 4326). The values of the coastline age raster per grid cell correspond to the most recent coastline position (in steps of 0.5 kyr). Values range from 0 (0 ka, i.e., present day) to 260 (26 ka) in bins of 5 (0.5 kyr). A value of “no data” is ascribed to pixels that have remained below sea level since 26 ka. Software format: All data processing was done using the R programming language

A complex hepatitis B virus (X/C) recombinant is common in Long An county, Guangxi and may have originated in southern China

Recently, a complex (X/C) hepatitis B virus (HBV) recombinant, first reported in 2000, was proposed as a new genotype; although this was refuted immediately because the strains differ by less than 8 % in nucleotide distance from genotype C. Over 13.5 % (38/281) of HBV isolates from the Long An cohort in China were not assigned to a specific genotype, using current genotyping tools to analyse surface ORF sequences, and these have about 98 % similarity to the X/C recombinants. To determine whether this close identity extends to the full-length sequences and to investigate the evolutionary history of the Long An X/C recombinants, 17 complete genome sequences were determined. They are highly similar (96–99 %) to the Vietnamese strains and, although some reach or exceed 8 % nucleotide sequence difference from all known genotypes, they cluster together in the same clade, separating in a phylogenetic tree from the genotype C branch. Analysis of recombination reveals that all but one of the Long An isolates resembles the Vietnamese isolates in that they result from apparent recombination between genotype C and a parent of unknown genotype (X), which shows similarity in part to genotype G. The exception, isolate QL523, has a greater proportion of genotype C parent. Phylogeographic analysis reveals that these recombinants probably arose in southern China and spread later to Vietnam and Laos

Seasonal Variation in TP53 R249S-Mutated Serum DNA with Aflatoxin Exposure and Hepatitis B Virus Infection

Background: Chronic hepatitis B virus (HBV) infection and dietary aflatoxin B1 (AFB1) exposure are etiological factors for hepatocellular carcinoma (HCC) in countries with hot, humid climates. HCC often harbors a TP53 (tumor protein p53) mutation at codon 249 (R249S). In chronic carriers, 1762T/1764A mutations in the HBV X gene are associated with increased HCC risk. Both mutations have been detected in circulating cell-free DNA (CFDNA) from asymptomatic HBV carriers

Hepatitis B Virus Impairs TLR9 Expression and Function in Plasmacytoid Dendritic Cells

Plasmacytoid dendritic cells (pDCs) play a key role in detecting pathogens by producing large amounts of type I interferon (IFN) by sensing the presence of viral infections through the Toll-Like Receptor (TLR) pathway. TLR9 is a sensor of viral and bacterial DNA motifs and activates the IRF7 transcription factor which leads to type I IFN secretion by pDCs. However, during chronic hepatitis B virus (HBV) infection, pDCs display an impaired ability to secrete IFN-α following ex vivo stimulation with TLR9 ligands. Here we highlight several strategies used by HBV to block IFN-α production through a specific impairment of the TLR9 signaling. Our results show that HBV particle internalisation could inhibit TLR9- but not TLR7-mediated secretion of IFN-α by pDCs. We observed that HBV down-regulated TLR9 transcriptional activity in pDCs and B cells in which TLR9 mRNA and protein levels were reduced. HBV can interfere with TLR9 activity by blocking the MyD88-IRAK4 axis and Sendai virus targeting IRF7 to block IFN-α production. Neutralising CpG motif sequences were identified within HBV DNA genome of genotypes A to H which displayed a suppressive effect on TLR9-immune activation. Moreover, TLR9 mRNA and protein were downregulated in PBMCs from patients with HBV-associated chronic hepatitis and hepatocellular carcinoma. Thus HBV has developed several escape mechanisms to avoid TLR9 activation in both pDCs and B lymphocytes, which may in turn contribute to the establishment and/or persistence of chronic infection