H5N1 avian influenza re-emergence of Lake Communication Qinghai: phylogenetic and antigenic analyses of the newly isolated viruses and roles of migratory birds in virus circulation

Highly pathogenic avian influenza H5N1 virus has swept west across the globe and caused serious debates on the roles of migratory birds in virus circulation since the first large-scale outbreak in migratory birds of Lake Qinghai, 2005. In May 2006, another outbreak struck Lake Qinghai and six novel strains were isolated. To elucidate these QH06 viruses, the six isolates were subjected to whole-genome sequencing. Phylogenetic analyses show that QH06 viruses are derived from the lineages of Lake Qinghai, 2005. Five of the six novel isolates are adjacent to the strain A/Cygnus olor/Croatia/1/05, and the last one is related to the strain A/duck/Novosibirsk/ 02/05, an isolate of the flyway. Antigenic analyses suggest that QH06 and QH05 viruses are similar to each other. These findings implicate that QH06 viruses of Lake Qinghai may travel back via migratory birds, though not ruling out the possibility of local circulation of viruses of Lake Qinghai.

塔里木盆地奥陶系不整合面岩溶作用特征与油气储层研究

Based on the principle and methods of carbonate sedimentology and reservoir geology, and guided by the theories of carbonate reservoir geology, the palaeokarst of Ordovician carbonate rocks in Tarim Basin has been comprehensively studied with multiple methods from different branches of geology. It is indicated that the features and distribution of palaeokarstification have developed in Ordovician carbonates. The controlling of karstification to Ordovician carbonate reservoirs has been discussed. Regional distribution of carbonate reservoirs controlled by karstification has been predicted within this basin. The main consents and conclusions of the this dissertation is as follows: Nine key indicators to the recognition of palaeokarst are proposed in terms of careful observation upon the well cores, lithological and geochemical analyses, and drilling and logging responses to the karst caves and fractures. The time and environment of cave filling are documented from careful research of lithofacies, mineralogy, and geochemistry of the physical and chemical fillings within karst caves. The caves in Ordovician carbonates were filled in Early Carboniferous in Lunnan area. The muddy filling in upper caves was deposited under subaerial fresh-water setting, while the muddy filling in lower caves was formed in the mixed water body of fresh-water and dominated sea water. Although most chemical fillings are suggested being precipated in the burial diagenetic environment after karstification but mineralogic and geochemical characteristics of some chemical fillings indicates they formed in meteoric environment during the karstification. It is obvious that the palaeokarst has been zoned in vertical profile. It can be divided into four units from top to bottom: surface karst, vadose karst, phreatic and tranquil flow zones. Between two types of limestone karst and dolostone karst are firstly differentiated in Tarim Basin, based on the comparison of features of each karst zone in limestone and dolostone regions. In Tabei area, the lowest depth of karstification is approximately 300 m below the Upper Ordovician unconformity interface, while the bottom depth of karstification in Tazhong area ranges commonly from 300 to 400 m, in rare cases may be up to 750 m below the upper Ordovician unconformity interface. In Lunnan and Tazhong areas, the palaeokarst morphology and the surface hydrosystem are firstly reconstructed based on the top of carboniferous "Shuangfeng limestone bed (Double-Peaks limestone)" as basal. According to the palaeomorphologic feature, karst topography can be divided into three units: karst upland, karst slope, and karst valley. Vadose zone was well developed in karst upland, and it can be found in a quite depth. Both vadose and phreatic zones were well developed in karst slope and upstream valley. In downstream valley, the karstification is not strong, the vadose and phreatic zones are thin in thickness. In Tazhong and Yingmaili areas, karstification is also developed in relict carbonate palaeo-hills which existed as isolated blocks admits clastic strata.

A study of carbon deposition on catalysts during the catalytic partial oxidation of methane to syngas in a fluidized bed

The deposition of carbon on catalysts during the partial oxidation of methane to syngas has been investigated in a fluidized bed. It was found that the relative rate of carbon deposition follows the order NiP > >d > Pt, Rh. Although the rate of carbon deposition in the fluidized bed was much lower than that in the fixed bed, carbon deposition could still be detected in the fluidized bed if a CH4/O-2 ratio in greater than 2.3 was used.

Heterogeneous asymmetric hydrogenation of ethyl pyruvate on chirally modified Pt/Al2O3 catalyst with fixed-bed reactor

The enantioselective hydrogenation of ethyl pyruvate on the cinchonidine modified Pt/Al2O3 catalyst was investigated using a high-pressure reaction system with a fixed-bed reactor for the purpose to produce the,chiral product without separating the catalyst from the reaction system. The reaction was also investigated in a batch reactor for comparison. About 60% e. e. and 90% e. e. were obtained with the fixed-bed reactor and the batch reactor respectively, demonstrating the possibility for the heterogeneous asymmetric hydrogenation in the fixed-bed reactor. Some adsorbed chiral modifier, cinchonidine, can be slowly removed from the surface of Pt/Al2O3 under the continuous flow reaction, as a result, the e, e, values drops with the reaction time in the fixed-bed reactor. The enantio-selectivity is higher in the fixed-bed reactor, but lower in the batch reactor when ethanol was used as solvent than that when acetic acid as solvent. CO was used as molecular probe to characterize the adsorption of cinchonidine an the catalyst surface by IR spectroscopy, A red shift observed in IR spectra of coadsorbed CO with cinchonidine suggests that the cinchonidine adsorption is mainly through the pi -interaction with platinum surface and donating electron to the platinum surface.

Review of Artificial Muscle Based on Contractile Polymers

An artificial muscle with strength and speed equal to that of a human muscle may soon be possible. Polymer gels exhibit abrubt volume changes in response to variations in their external conditions -- shrinking or swelling up to 1000 times their original volume. Through the conversion of chemical or electrical energy into mechanical work, a number of devices have already been constructed which produce forces up to 100N/cm2 and contraction rates on the order of a second. Through the promise of an artificial muscle is real, many fundamental physical and engineering questions remain before the extent or limit of these devices is known.

Dynamic Model and Control of an Artificial Muscle Based on Contractile Polymers

A dynamic model and control system of an artificial muscle is presented. The artificial muscle is based on a contractile polymer gel which undergoes abrupt volume changes in response to variations in external conditions. The device uses an acid-base reaction to directly convert chemical to mechanical energy. A nonlinear sliding mode control system is proposed to track desired joint trajectories of a single link controlled by two antagonist muscles. Both the model and controller were implemented and produced acceptable tracking performance at 2Hz.

Ligand modified real heterogeneous catalysts for fixed-bed hydroformylation of propylene

A novel ligand modified heterogeneous catalyst has been developed for hydroformylation of propylene, which showed excellent activity, selectivity and stability and need not be separated from the product after reaction in a fixed-bed reactor. The coordination bonds between triphenyl phosphine (PPh3) and Rh/SiO2 were confirmed by means of thermogravimetric (TG), solid-state P-31 NMR, XPS and FT-IR. Two types of active species for hydroformylation were formed, which were proved by in situ FT-IR techniques. The problem of metal leaching was greatly reduced by directly fastening Rh particles on the support, and the active Rh species that was responsible for the outstanding performance of propylene hydroformylation was tightly bound by the very strong metal-metal bonds. No sign of deactivation was observed over a period of more than 1000 h on the condition that PPh3 was added at 300-350 h of time on stream. (c) 2005 Elsevier B.V. All rights reserved.