Porous SnO(2) nanospheres with high surface areas have been synthesized through a solvothermal method in the absence of any templates. The structure and morphology of the resultant products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and nitrogen adsorption-desorption technique. The as-prepared SnO(2) porous nanospheres with the diameters ranging from 90-150 nm are composed of small nanocrystals with average sizes of less than 10 nm. Results demonstrated that the formation of porous SnO(2) nanospheres is ascribed to etching the center part of the nanospheres. It was found that hydrochloric acid and NaClO played important roles in determining the final morphologies of the porous SnO(2) nanospheres. The gas sensing properties of the as-prepared porous SnO(2) nanospheres were investigated. By the comparative gas sensing tests, the porous SnO(2) nanospheres exhibited a superior gas sensing performance toward ppb level 2-chloroethanol and formaldehyde vapor, implying promising applications in detecting toxic volatile organic compounds (VOCs).

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The reindeer is an Arctic species that exhibits distinctive biological characteristics, for which the underlying genetic basis remains largely unknown. We compared the genomes of reindeer against those of other ruminants and nonruminant mammals to reveal the genetic basis of light arrhythmicity, high vitamin D metabolic efficiency, the antler growth trait of females, and docility. We validate that two reindeer vitamin D metabolic genes (CYP27B1 and POR) show signs of positive selection and exhibit higher catalytic activity than those of other ruminants. A mutation upstream of the reindeer CCND1 gene endows an extra functional binding motif of the androgen receptor and thereby may result in female antlers. Furthermore, a mutation (proline-1172→threonine) in reindeer PER2 results in loss of binding ability with CRY1, which may explain circadian arrhythmicity in reindeer.

BackgroundThe reindeer (Rangifer tarandus) is the only fully domesticated species in the Cervidae family, and it is the only cervid with a circumpolar distribution. Unlike all other cervids, female reindeer, as well as males, regularly grow cranial appendages (antlers, the defining characteristics of cervids). Moreover, reindeer milk contains more protein and less lactose than bovids’ milk. A high-quality reference genome of this species will assist efforts to elucidate these and other important features in the reindeer.FindingsWe obtained 615 Gb (Gigabase) of usable sequences by filtering the low-quality reads of the raw data generated from the Illumina Hiseq 4000 platform, and a 2.64-Gb final assembly, representing 95.7% of the estimated genome (2.76 Gb according to k-mer analysis), including 92.6% of expected genes according to BUSCO analysis. The contig N50 and scaffold N50 sizes were 89.7 kilo base (kb) and 0.94 mega base (Mb), respectively. We annotated 21 555 protein-coding genes and 1.07 Gb of repetitive sequences by de novo and homology-based prediction. Homology-based searches detected 159 rRNA, 547 miRNA, 1339 snRNA, and 863 tRNA sequences in the genome of R. tarandus. The divergence time between R. tarandus and ancestors of Bos taurus and Capra hircus is estimated to be about 29.5 million years ago.ConclusionsOur results provide the first high-quality reference genome for the reindeer and a valuable resource for studying the evolution, domestication, and other unusual characteristics of the reindeer.

In2O3 nanofibers and nanoribbons were prepared by electrospinning combined with a poly(vinyl pyrrolidone)‐assisted sol–gel technique. By tuning the experimental parameters, the morphological transformation of In2O3 from nanofibers to nanoribbons was achieved. It was found that both the rapid evaporation of solvent and the concentration of the precursor played important roles in the formation process of In2O3 nanoribbons. The average diameter of the In2O3 nanofibers is 180 nm. The nanoribbons have an average width of 1 μm and a thickness of about 150 nm. The lengths of both can reach millimeters. The average grain size consisting of nanofibers and nanoribbons is 18.6 and 11.2 nm, respectively. The gas‐sensing properties of In2O3 nanofibers and nanoribbons toward formaldehyde vapor were investigated. Interestingly, the gas sensor fabricated with In2O3 nanoribbons exhibited a higher and faster response at a relatively lower operating temperature than that fabricated with nanofibers.

Yak (Bos grunniens) is an important and dominant livestock species in the challenging environment of the Qinghai-Tibetan Plateau. Rumen microbiota of the solid, liquid, and epithelium fractions play key roles in nutrient metabolism and contribute to host adaptation in ruminants. However, there is a little knowledge of the microbiota in these rumen fractions of yak. Therefore, we collected samples of solid, liquid, dorsal, and ventral epithelium fractions from five female yaks, then amplified bacterial 16S rRNA gene V4 regions and sequenced them using an Illumina MiSeq platform. Principal coordinates analysis detected significant differences in bacterial communities between the liquid, solid, and epithelium fractions, and between dorsal and ventral epithelium fractions. Rikenellaceae RC9, the families Lachnospiraceae and Ruminococcaceae, and Fibrobacter spp. were the abundant and enriched bacteria in solid fraction, while the genera Prevotella and Prevotellaceae UCG 003 were higher in the liquid fraction. Campylobacter spp.,Comamonas spp., Desulfovibrio spp., and Solobacterium spp. were significantly higher in dorsal epithelium, while Howardella spp., Prevotellaceae UCG 001, Ruminococcaceae UCG 005, and Treponema 2 were enriched in the ventral epithelium. Comparison of predictive functional profiles among the solid, liquid, and dorsal, and ventral epithelium fractions also revealed significant differences. Microbiota in the ventral fraction of yak rumen also significantly differ from reported microbiota of cattle. In conclusion, our results improve our knowledge of the taxonomic composition and roles of yak rumen microbiota. K E Y W O R D SBos grunniens, Campylobacter spp., dorsal and ventral epithelium, ecology niches, Howardella spp, rumen, solid and liquid

Simple SummarySoybean meal is a major protein ingredient in ruminant diets. However, the swine and poultry industries are also competitors for soybean meal as their primary protein ingredient. Thus, soybean meal is expensive, and actually the most expensive gradient of ruminant diets. In this context, urea is used as a low-cost nitrogen source to replace up to 75% of the soybean meal typically fed to fattening lambs. Urea at 10 g could substitute 130 g soybean meal per kg feed dry matter without adverse effects on digestion, metabolism, or growth in fattening lambs when fed a high concentrate diet.AbstractThis study investigated the effects of partially substituting soybean meal (SBM) with incremental amount of urea on rumen fermentation, nutrient digestion, plasma metabolites, and growth performance in fattening lambs. Seventy fattening male lambs were sorted into two blocks according to body weight (BW) and assigned to one of five dietary treatments in a randomized block design: SBM at 170 g/kg dry matter (DM) or reduced SBM (40 g/kg DM) plus 0, 10, 20, or 30 g urea/kg DM. Compared with the lambs receiving the SBM diet, the lambs fed the reduced SBM diet plus urea had higher (p < 0.01) concentrations of ruminal ammonia, and the ruminal concentration of ammonia also increased linearly (p < 0.01) with the increasing urea supplementation. Linear and quadratic effects (p < 0.01) on the crude protein (CP) intake and digestibility were observed with the increasing urea addition to the diet. The concentrations of plasma ammonia and blood urea nitrogen (BUN) increased (linear, p < 0.01; quadratic, p < 0.01) with the increasing urea supplementation. The final BW, DM intake (DMI), average daily gain (ADG), and gain efficiency were similar (p ≥ 0.42) between the SBM group and the urea-supplemented groups. However, the DMI and ADG increased quadratically (p ≤ 0.03) with the increasing urea addition to the diet, with the 10 g urea/kg DM diet resulting in the highest DMI and ADG. The results of this study demonstrated that 10 g urea could substitute 130 g soybean meal per kg feed DM without any adverse effect on growth performance or health in fattening lambs when fed a high concentrate diet.

Berberine (BBR) shows very low plasma levels after oral administration due to its poor absorption by the gastrointestinal tract. We have previously demonstrated that BBR showed increased gastrointestinal absorption and enhanced antidiabetic effects in db/db mice after being entrapped into solid lipid nanoparticles (SLNs). However, whether BBR-loaded SLNs (BBR-SLNs) also have beneficial effects on hepatosteatosis is not clear. We investigated the effects of BBR-SLNs on lipid metabolism in the liver using histological staining and reverse transcription polymerase chain reaction analysis. The results showed that oral administration of BBR-SLNs inhibited the increase of body weight and decreased liver weight in parallel with the reduction of serum alanine transaminase and liver triglyceride levels in db/db mice. The maximum drug concentration in the liver was 20-fold higher than that in the blood. BBR-SLNs reduced fat accumulation and lipid droplet sizes significantly in the liver, as indicated by hematoxylin and eosin and Oil Red O staining. The expression of lipogenic genes, including fatty acid synthase ( FAS ), stearoyl-CoA desaturase ( SCD1 ), and sterol regulatory element-binding protein 1c ( SREBP1c ) were downregulated, while lipolytic gene carnitine palmitoyltransferase-1 ( CPT1 ) was upregulated in BBR-SLN-treated livers. In summary, we have uncovered an unexpected effect of BBR-SLNs on hepatosteatosis treatment through the inhibition of lipogenesis and the induction of lipolysis in the liver of db/db mice.