In the past few years, we have performed a 22 GHz H2O maser survey towards hundreds of BGPS sources using the 25-meter Nanshan Radio Telescope (NSRT) of the Xinjiang Astronomical Observatory, and detected more than one hundred masers. Our aim is to study star formation activities associated with these sources, as well as search for any correlations that may exist between 22 GHz H2O masers and the evolutionary stage of high-mass star formation regions. The NSRT has been upgraded and have now an effective diameter of 26 meter. Besides, cryogenically cooled dual-beam receiver systems covering seven millimeter-wave observing bands have been installed on the NSRT. For the next step of maser observation, we will continue to do H2O and SiO masers survey of massive dust clumps and monitor some maser sources.

In this paper we present new petrological and whole-rock geochemical data for the Palaeoproterozoic metasedimentary rocks in the upper part of the Ji'an Group within the Jiao–Liao–Ji Belt, China, as well as zircon U–Pb age dates and in situ Lu–Hf isotope data. The new data improve our understanding of the original nature of the metasedimentary rocks, further providing insights into their tectonic setting and the evolutionary history of the northern segment of the Jiao–Liao–Ji Belt. The zircons can be divided into two groups, viz., one of magmatic origin and the other of metamorphic origin. Zircon U–Pb dating gave mean or statistical peak ages for the magmatic zircons at 2035, 2082, 2178, 2343–2421, 2451–2545, 2643–2814 and 2923–3446 Ma, and mean peak ages for the metamorphic zircons at 1855 and 1912 Ma, which indicate a maximum depositional age of 2.03 Ga and two-stage metamorphic events at c. 1.91 and 1.85 Ga for the metasedimentary rocks. Geochemical data show that (1) the protoliths of these rocks were mainly sandstones, greywackes and claystones, together with some shales; (2) the main sources of the sedimentary material were Palaeoproterozoic granites and acid volcanic rocks, with minor contributions from Archaean granitic rocks; and (3) the sediments were deposited in an active continental margin setting. Moreover, along the northeastern margin of the Eastern Block of the North China Craton there is evidence of ancient crustal materials as old as 3.76 Ga, and multiple crustal growth events at 3.23–3.05, 2.80–2.65, 2.54–2.45 and 2.28–2.08 Ga.

Red-emitting (La,Eu)2O2SO4 phosphors have been successfully prepared using the layered hydroxide of (La,Eu)2(OH)4SO4·2H2O as the precursor. The precursor compound was firstly crystallized via hydrothermal reaction (100 °C and pH = 9.0) as well-dispersed nanoplates, followed by dehydration and dehydroxylation in the 400–1200 °C temperature range in ambient air to yield (La,Eu)2O2SO4. The phosphors show intense red emissions originated from the f–f transitions of Eu3+, dominantly peaking at 617 nm, under O–Eu charge transfer excitation at 284 nm. The optimal Eu3+ content was experimentally determined to be 5 at.%, agreeing well with theoretical analysis, and the concentration quenching of luminescence was suggested to be due to exchange interactions. Fluorescence decay analysis indicates that a higher calcination temperature or Eu3+ content would decrease the lifetime of the 617 nm emission.

The present study was designated to ascertain the anthelmintic activity of the rhizomes of Paris polyphylla and to isolate and characterize the active constituents. The methanol extract from rhizomes of P. polyphylla showed significant anthelmintic activity against Dactylogyrus intermedius with the median effective concentration (EC50) 22·5 mg L−1. Based on this finding, the methanol extract was fractionated by silica gel column chromatography in a bioassay-guided fractionation yielding 2 bioactive compounds, the structures of these compounds were elucidated as formosanin C and polyphyllin VII. The in vivo tests revealed that formosanin C and polyphyllin VII were significantly effective against D. intermedius with EC50 values of 0·6 and 1·2 mg L−1, respectively. The acute toxicities (LC50) of formosanin C and polyphyllin VII for grass carp were 2·8 and 2·9 mg L−1, respectively. The overall results provide important information for the potential application of formosanin C and polyphyllin VII in the therapy of serious infection caused by D. intermedius.

High-concentration niobium (V)-doped titanium dioxide (TiO2) nanoparticles of the nonequilibrium chemical composition have been synthesized via Ar/O2 radio-frequency thermal plasma oxidation of mist precursor solutions with various Nb5+ concentrations (Nb/(Ti + Nb) = 0–25.0 at.%). The solubility as high as ∼25.0 at.% has not been achieved before by wet-chemical techniques. The preferable anatase formation was attained in the plasma-synthesized powders and was enhanced by the niobium doping. All the powders were heated at high temperatures (600–800 °C) to investigate their phase transformation, band gap variation, inter-particulate binding behavior, and photocatalytic stability. The transformation from anatase to rutile was effectively inhibited by increasing the Nb5+ content. The Nb5+ doping prevented the band gap of TiO2 from narrowing after the heating. At high temperatures, Nb5+ doping could not only preserve particle size but also prevent inter-particulate binding. High concentration (25.0 at.%) Nb5+ doping retained the photocatalytic performance almost invariably irrespective of being thermally treated.

Consumption of resistant starch (RS)-enriched foods is associated with decrease in the postprandial glycaemic and insulinaemic responses, accompanied by the production of fermentation-related gases in the large bowel. The present study aimed to determine the postprandial glycaemic and insulinaemic responses to the GM RS-enriched rice and the fermentation-related production of H2 in young and healthy Chinese adults. A total of sixteen young adults (nine men and seven women) were recruited and divided into three groups. Their postprandial glycaemic and insulinaemic responses to 40 g glucose, carbohydrates of RS or wild-type (WT) rice were tested by a crossover model with a washout period of 7 d. The concentrations of blood glucose and insulin as well as breath H2 were measured before and after food intake. Although the mean concentrations of fasting blood glucose, insulin and breath H2 were similar, consumption of the RS rice significantly decreased the values of glycaemic index (GI) and insulin index (II), as compared with the intake of WT rice (48·4 (sem 21·8) v. 77·4 (sem 34·9) for GI, 34·2 (sem 18·9) v. 54·4 (sem 22·4) for II, P < 0·05), respectively. Conversely, intake of the RS rice meal significantly elevated the concentrations of breath H2, as compared with WT rice (38·9 (sem 17·6) v. 10·5 (sem 3·7) parts per million for peak levels of breath H2, P < 0·05) through a period of 16-h tests. Consumption of the GM RS-enriched rice meal decreased the postprandial glycaemic and insulinaemic responses and promoted RS fermentation-related production of H2 in the large bowel of young and healthy Chinese adults.

The outcome of Plasmodium yoelii 17XL-infected BALB/c and DBA/2 mice, ranging from death to spontaneous cure, respectively, depends largely on the establishment of effective pro-inflammatory type 1 responses during the early stages of infection and associates with CD4+CD25+Foxp3+regulatory T cells (Tregs). Here, effects of Tregs were analysed on early P. yoelii 17XL infection in BALB/c and DBA/2 mice. In vivo depletion of Tregs significantly reversed the inhibited establishment of effective pro-inflammatory type 1 responses in BALB/c mice, indicating that this cell population contributed to the suppression of T-cell function in malaria. Moreover, the proportion and absolute numbers of IL-10-secreting Tregs in BALB/c mice were significantly higher than that found in DBA/2 mice by intracytoplasmic staining, and IL-10 production was correlated with the Tregs population. In addition, in vivo Tregs depletion decreased the production of IL-10 and the apoptosis of CD4+ T cells. Consistently, IL-10R blockade also had the same effect as that of Tregs depletion in P. yoelii 17XL-infected BALB/c mice. Our data demonstrate that Tregs perhaps have an important role in regulating pro-inflammatory type 1 responses in an IL-10-dependent manner and induce CD4+ T cell apoptosis during the early stage of P. yoelii 17XL infection.

Titanium dioxide nanopowders were synthesized by in-flight oxidation of titanium nitride (TiN) in radio-frequency (rf) induction thermal plasma. The powders were characterized by x-ray diffraction, high-resolution transmission electron microscopy, field emission scanning electron microscopy, Raman spectroscopy, and optical microscopy to reveal the mechanisms of phase selection and particle morphology evolution. The reaction began with surface oxidation of TiN particles, leading to the formation of core-shell composites with oxidized shells and TiN cores, followed by gas-phase condensation of TiO2 nanoparticles. Phase selection of the resultant TiO2 powders was found to largely depend on the oxidation potential of the thermal plasma rather than on the heat transfer itself. Anatase content of the products increased steadily with increasing the O2 input, and TiO2 nanoparticles (∼50 nm) containing ∼90% of anatase were obtained through O2/Ar plasma treatment. Phase-pure rutile nanoparticles (∼50 nm, on average) were also synthesized in H2/Ar plasma injected with O2 as the powder carrier gas.

A basic sulfate precursor [Sc(OH)SO4·2H2O] for well-sinterable Sc2O3 powders was precipitated from mixed solutions of scandium nitrate [Sc(NO3)3] and ammonium sulfate [(NH4)2SO4] at room temperature and which was subsequently converted to Sc2O3 via dehydroxylization and desulfurization at temperatures ≥900 °C. With the reactive powders synthesized in this work, polycrystalline Sc2O3 ceramics showing high inline transmittances of approximately 70% in the visible wavelength region (corresponding to ∼90% of the theoretical value of single crystals) have been fabricated via vacuum sintering at a relatively low temperature of 1700 °C.

Scandia (Sc2O3) is a ceramic material that shows interesting thermal and optical properties, but is difficult to grow as single crystals. As an alternative, in this work we fabricated polycrystalline Sc2O3 transparent ceramics via vacuum sintering, using powders thermally pyrolyzed at 1200 °C from a scandium sulfate salt, Sc2(SO4)3 · 7.8H2O, that we prepared. Characterization of the powders was achieved by differential thermal analysis/thermogravimetry, x-ray diffractometry, Brunauer–Emmett–Teller analysis, and field-emission scanning electron microscopy. Sintering behaviors of the Sc2O3 powders were studied in air via dilatometry. The sulfate salt transforms to oxide at temperatures ≥1000 °C, and the best pyrolysis temperature for transparent ceramics fabrication is 1200 °C, at which the resultant Sc2O3 powder is good in dispersion, ultrafine in particle size (∼80 nm), and almost free from residual sulfur. Transparent ceramics were fabricated from this powder via vacuum sintering at 1625 °C or above. The ceramics sintered at 1700 °C for 4 h exhibit an in-line transmittance of approximately 56–58% in the visible light region at a sample thickness of 1.0 mm.

Monodispersed Sc2O3 precursor particles were synthesized by the urea-based homogeneous precipitation method, with an investigation into the effects of supporting anions (NO3−, Cl−, and SO4 2−) on powder properties. Characterizations of the powders were achieved by elemental analysis, x-ray diffractometry, Fourier transform infrared, differential thermal analysis/thermogravimetry, high-resolution scanning electron microscopy, and the Brunauer-Emmett-Teller method. Unlike other rare earths, Sc3+ does not precipitate as basic carbonate but instead forms hydrated γ-ScOOH from either nitrate or chloride solution. Particles of the hydrated γ-ScOOH are pumpkin-shaped (approximately 1.0 μm) and are made up of thin-platelike crystallites emanating from a common axis. The presence of complexing SO42− changes the reaction chemistry toward Sc2O3 powders, leading to basic sulfate [Sc(OH)1.6(SO4)0.7 η H2O] precursor particles having hexagonal morphology (approximately 10 μm in diameter and 0.5 μm in thickness). The hydrated γ-ScOOH directly converts to Sc2O3 by calcination at 400 °C or above, while the basic sulfate transforms to oxide at temperatures ≥ 900 °C via an amorphous state and a Sc2(SO4)3 intermediate. The effect of SO42− on powder morphologies and reaction chemistry is discussed. Nanocrystalline Sc2O3 powders comprising monodispersed particles were obtained via thermal decomposition of the precursors.

A carbonate coprecipitation method was used for the facile synthesis of highly reactive 10 mol%-Y2O3-doped CeO2 (20YDC) nanopowders, employing nitrates as the starting salts and ammonium hydrogen carbonate (AHC) as the precipitant. The AHC/RE3+ (RE = Ce + Y) molar ratio (R) and the reaction temperature (T) significantly affect the final yield and precursor properties, including chemical composition and particle morphology. Suitable processing conditions are T = 60 °C and R = 2.5 to 10, under which precipitation is complete, and the resultant precursors show ultrafine particle size, spherical particle shape, and good dispersion. The thus-processed precursors are basic carbonates with an approximate formula of Ce0.8Y0.2(OH)CO3 · 2H2O, which directly yield oxide solid solutions upon thermal decomposition at a very low temperature of approximately 400 °C. The 20YDC solid-solution powders calcined at 700 °C show excellent reactivity and were densified to >99% of theoretical via pressureless sintering at a very low temperature of 950 °C for 6 h.

The influence that trace concentrations of SiO2 have on improving grain-boundary conduction via precursor scavenging using additional heat treatment at 1200 °C for 40 h before sintering was investigated. At a SiO2-impurity level (SIL) ≤160 ppm by weight, the grain-boundary resistivity (ρgb) decreased to 20% of its value, while no improvement in grain-boundary conduction was found at a SIL ≥ 310 ppm. The correlation between the resistance per unit grain-boundary area, rgb, and average grain size indicated that the inhomogeneous distribution of the siliceous phase in the sample with a SIL ≥ 310 ppm hampered the scavenging reaction.

The interaction between nucleus and cytoplasm can be explored through nuclear transfer. We describe here another tool to investigate this interaction: MII meiotic apparatus transfer (MAT) between mouse oocytes. In this study, the MII oocyte meiotic apparatus or spindle from C57BL/6 mice, a black strain, was transferred into an enucleated metaphase oocyte from Kunming mouse, a white strain. The results showed that the enucleation rate by treating oocytes with 3% sucrose was 100%, but the electrofusion efficiency was very low, with only 17.6% of reconstructed karyoplast-recipient cytoplasm pairs fused. When the fused oocytes were exposed to spermatozoa from C57BL/6 mice, 9 of 11 (82%) were fertilised. Eight reconstructed embryos at 1- to 4-cell stages were transferred into the oviducts of two synchronously pregnant Kunming strain fosters and one delivered two normal C57BL/6 offspring. This study indicates that MII meiotic apparatus or spindle sustains normal structure and function after micromanipulation and electrofusion. MAT provides a model for further research on the application of this technique to assisted human reproduction.

Stoichiometric yttrium aluminate garnet (Y3Al5O12) precursors with a wide range of chemical compositions were precipitated by dripping a mixed solution of ammonium aluminum sulfate and yttrium nitrate into ammonium bicarbonate solutions. The resultant precursors were characterized by chemical analysis, infrared spectroscopy, differential thermal analysis/thermogravimetry, x-ray diffractometry, and scanning electron microscopy. The effects of reaction temperature, precipitant concentration, dripping speed of the salt solution, and the molar ratio of precipitant/total-cations on the composition, thermal behavior, and particle morphology of the resultant precursors were investigated. The precipitation conditions that yield carbonate precursors composed of ammonium dawsonite [NH4Al(OH)2CO3] and yttrium normal carbonate [Y2(CO3)3 · 3H2O] were determined.

Ammonium hydrogen carbonate was used as the precipitant to synthesize yttrium aluminate garnet (YAG) precursors from a mixed solution of aluminum and yttrium nitrates via coprecipitation. The carbonate precursor, with an approximate composition of NH4AlY0.6(CO3)1.9(OH)2 · 0.8H2O, transformed to pure YAG at 900 °C without the formation of intermediate phases. Reactive YAG powder was produced by calcining the precursor at 1100 °C. The YAG powder densified to 99.8% of the theoretical density by vacuum sintering at 1500 °C for 2 h, and the sintered body showed transparency. Less agglomeration of the precursor and good dispersity of the resultant YAG powder were responsible for the excellent sinterability.

Carbonate precursors of Y3Al5O12 (YAG) were synthesized from a mixed solution of alum and yttrium nitrate using ammonium hydrogen carbonate as precipitant. Precipitation method (normal-strike or reverse-strike) and aging were found to have dramatic effects on cation homogeneity of the precursor, which in turn influenced the formation temperature of the YAG phase. Reactive YAG powders were produced from the reverse-strike-derived, as-synthesized precursors at temperatures ≤1200 °C. These powders densified to >98.0% of the theoretical density up to 1500 %C at a constant heating rate of 8 %C/min or to transparency by vacuum sintering at 1700 %C for 1 h without additives.