大功率气体发动机电子节气门设计与研究

以大功率气体发动机的电子节气门为研究对象,对其进行了系统的设计和研究。在分析电子节气门机械结构的基础上,建立了电子节气门数学模型,采用冗余设计思想设计了双H桥电子节气门驱动电路。采用增量式PID控制算法对电子节气门开度进行精确的闭环控制。实验结果表明,设计的电子节气门系统鲁棒性好,具有很好的响应性和稳定性,能满足大功率气体发动机的性能需求。     

江西双季稻机插的典型模式及其效果研究

基于江西省双季稻区10个县30个乡镇农户、合作社以及农机大市场的调查数据,通过对合作社的两种典型模式（合作模式和服务模式）的研究及合作社农户和散户的对比分析,探索合作社对江西双季稻机插推广的促进作用。研究结果表明:合作社农户的成本要低于散户,收益要高于散户,合作社的生产效果比散户的要好;合作社农户的年龄比散户的年龄要低,文化、土地规模、资金要高于散户;合作社农户的机插比例高于散户;目前江西合作社机插典型模式中比较受欢迎的模式是农机大户和种田大户合作模式及“订单式”服务模式;未来种田大户、农机大户和养殖大户是发展江西农民合作生产的主要对象,重点发展的模式是合作社提供水稻生产全程社会化服务模式。     

全膜双垄沟双幅覆膜覆土联合作业机设计与试验

为进一步提升全膜双垄沟覆膜种床机械化耕整作业效果与作业效率,基于全膜双垄沟种床双幅覆膜覆土农艺技术栽培模式,设计全膜双垄沟双幅覆膜覆土联合作业机,实现了全膜双垄沟种床构建过程中的旋耕、起垄、施肥、双幅覆膜覆土及镇压的一体化作业。在设定联合作业机传动系统的前提下,对样机关键部件进行设计与选型,确定其旋耕刀组、排肥装置、提土-种床覆土装置的工作参数与功耗,同时解析了刮板式提土装置、水平双向螺旋输土装置作业过程,得到满足双幅覆膜种床各部位覆土的必要条件。应用离散单元法对提土-种床覆土装置"提土-输土-覆土"动态作业过程进行数值模拟,分析了各工作环节输土、覆土特性,对影响覆土作业效果的相关因素进行了探讨。田间试验结果表明,当全膜双垄沟双幅覆膜覆土联合作业机前进速度为1. 10 m/s时,采光面地膜机械破损程度为39. 8 mm/m~2、种床膜边覆土宽度合格率为94. 5%、大垄垄体中心覆土宽度合格率为91. 6%、种床覆土厚度合格率为97. 5%、种床起垄高度合格率为93. 2%,试验指标均符合国家与行业标准要求,试验结果满足设计和实际作业要求,田间试验工况与仿真结果基本一致。     

双斜盘多排式轴向柱塞马达转矩特性分析

为了实现多级转速和转矩的输出,轴向柱塞马达必须使用节流阀、减压阀等耗能元件来改变输入压力和流量,但同时降低了效率。新型双斜盘多排式轴向柱塞马达可以利用其结构的特殊性,实现输出转矩的多样性。本文基于双斜盘多排式轴向柱塞马达的结构特点及工作原理,推导了该马达在不同工作方式下的理论瞬时转矩和转矩不均匀系数,并通过Matlab分析了内外马达转矩系数比对转矩不均匀系数的影响,设计了马达的实验液压系统并搭建了实验平台,对马达进行了原理性实验,并进行了数据分析。实验结果表明,在额定压力和额定排量下,该马达能实现多种不同的转速与转矩输出,随着内外马达转矩系数比的增大,低速大转矩的转矩不均匀系数越小,高速低转矩不稳定系数越大,通过合理设计可以实现马达在不同工作状态下的稳定运行,验证了新型马达在结构原理上的可行性,为新型轴向柱塞马达的改进设计提供了实验依据。     

PCV2 Rep蛋白N-糖基化位点突变对病毒复制的影响

N-糖基化对病毒的感染与增殖均具有重要作用,与PCV2复制相关的Rep蛋白含有三个N-糖基化位点。为了分析PCV2Rep蛋白N-糖基化位点突变对病毒复制的影响,本试验构建了三个双拷贝突变体感染性克隆2M23、2M256、2M286,并成功拯救病毒。通过间接免疫荧光检测病毒的拯救效果,TCID50测定病毒的感染力,荧光定量PCR检测细胞病毒的载量。结果显示,PCV2Rep蛋白的23~25aa、256~258aa N-糖基化位点突变后降低病毒的复制能力,而286~288aa突变后增强病毒的复制能力,为进一步阐明PCV2的复制及致病机制提供参考。     

Effects of different forms and origins of oilseeds on dynamics of ruminal biohydrogenation of long‐chain fatty acids in vitro

Dietary unsaturated fatty acids (FA) are intensively hydrogenated in the rumen, resulting in reduced amount of poly‐unsaturated fatty acids (PUFA) and accumulation of several biohydrogenation (BH) products. In this study, BH of PUFA originating from different oilseeds (linseed, soya beans, sunflower seed and rapeseed) present in crushed oilseeds or their free oils were assessed in vitro. The assay substrates were incubated in buffered rumen fluid for 0, 6, 12 and 24 h. After incubation, the FA pattern of the incubated samples was analysed using gas chromatography. Biohydrogenation is defined as disappearance of double bonds (DB) calculated from the contents of unsaturated FA. After 24‐h incubation, the DB contents of all oilseeds were reduced (p < 0.001) by 40–60%. The reduction was higher (p < 0.001) for the crushed form compared with the oil form. In addition, linseed and sunflower seed known as oilseeds with high contents of linolenic acid C18:3 c9,12,15 (LNA) and linoleic acid C18:2 c9,12 (LA), respectively, showed a higher (p < 0.001) accumulation of the BH intermediates conjugated linoleic acid (CLA, isomer C18:2 c9t11) and vaccenic acid (C18:1 t11) for the crushed form, when compared with the oil. These results suggest an inherent effect of the physical form of the assay oilseeds on in vitro BH. Changes in FA pattern during BH in vitro can be attributed to both source and physical form of the assay oilseeds. However, further investigations are warranted to ensure whether the observed in vitro effects on ruminal BH can be confirmed in vivo.     

不同氮素水平下双季稻株型与冠层内光截获特征研究

本文旨在阐明双季稻株型与冠层内光合有效辐射截获的时空分布特征。选用4个不同株型早、晚稻品种,设置4个不同施氮水平,系统观测其植株形态和冠层内光合有效辐射截获率(IPAR)的时空分布状况。结果表明,施氮水平对早、晚稻株高、穗长、叶长和叶基角均有显著影响,均表现为随施氮水平的增加而增大;早、晚稻孕穗期的分层叶面积指数(LAI)和向上累积LAI大于抽穗后12 d,分层LAI呈冠层中部大于上部和下部的分布特征,最大分层LAI出现在0.58相对高度处;冠层上中部分层LAI和向上累积LAI随施氮水平的增加而增大;向上累积LAI随相对高度呈S型曲线分布,可用Logistic方程定量描述(R~2 0.99);早、晚稻孕穗期的冠层IPAR大于抽穗后12 d,且随施氮水平的增加而增大,其日变化表现为正午较小,早晚较大;株型紧凑的早、晚稻品种,冠层IPAR低;冠层IPAR与向下累积LAI之间的关系可用方程IPAR=a (1-e~(-b×LAI))定量描述(R~2 0.88);冠层内IPAR的三维空间分布表现为冠层上中部水平面上IPAR较低,光斑变化大,冠层下部水平面上IPAR较高,光斑变化较平缓,同一冠层高度水平面上的IPAR呈不均匀分布。研究结果可为双季稻高产栽培及理想株型的优化设计提供支撑。     

Neuroprotective effect of novel Rho kinase inhibitor FSD-C10 on a mouse model of Alzheimer disease

AIM: To explore the neuroprotective effect of novel Rho kinase inhibitor FSD-C10 on Alzheimer disease (AD) model of APP/PS1 double transgenic (Tg) mice. METHODS: Male APP/PS1 Tg mice (n=20) at 8 months of age were randomly divided into 2 groups:model group and FSD-C10 treatment group. The mice were treated with normal saline or FSD-C10 (25 mg·kg^-1·d^-1) by intraperitoneal injection, once daily for 2 months. Age-and sex-matched wild-type (WT) mice without treatment were used as the control. The Morris water maze (MWM) test and SMART 3.0 behavioral record system were applied to examine and analyze the spatial cognitive function of the mice. The protein levels and distribution of Aβ, p-tau and synapse-associated proteins such as synaptophysin, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) and postsynaptic density protein 95 (PSD-95) were determined by immunofluorescence staining. The protein levels of phosphorylated amyloid precursor protein at Thr668[p-APP(Thr668)], beta-site APP-cleaving enzyme 1 (BACE1) and synapse-associated proteins in the brain were analyzed by Western blot. RESULTS: Compared with model group, FSD-C10 treatment significantly improved the cognitive function of the APP/PS1 Tg mice, accompanied by reduced Aβ deposition and p-tau level, increased protein level of p-APP (Thr668) in the central nervous system, decreased expression of BACE1, and increased expression of synapse-associated proteins in the brain of the mice (P<0.05). CONCLUSION: FSD-C10 has neuroprotective potential in the APP/PS1 Tg mice. The mechanism may be related to enhancing the non-amyloidogenic APP cleavage pathway, reducing the production of Aβ oligomers, the deposition of senile plaques and the amount of tau protein, up-regulating synapse-associated proteins, and increasing synaptic plasticity.     

线性红利界下带干扰风险模型的破产概率

考虑到保险公司在实际经营中收益所具有的不确定性和分红策略，建立一类具有线性红利界和带随机扰动的双复合Poisson风险模型，利用鞅方法给出模型关于破产概率的一个定理及上界．     

鸡白细胞介素-6原核表达及双抗夹心ELISA方法的建立

应用分子生物学技术原核表达ChIL-6，以ChIL-6重组蛋白为免疫原，按免疫程序分别制备兔抗和鼠抗IL-6重组蛋白的多克隆抗体。应用此抗体建立双抗夹心EL-ISA方法后，为了优化此方法本试验对该方法的最佳试验条件、标准曲线、重复性和初步应用进行确定。结果显示，经SDS-PAGE和Western-blot分析，表明ChIL-6在大肠杆菌中正确表达，为了建立检测ChIL6的双抗夹心ELISA方法，本试验应用表达的重组蛋白制备兔抗和鼠抗多克隆抗体。建立的双抗夹心ELISA方法最佳反应条件为包被抗体的质量浓度为50mg／L，4℃过夜；酶标二抗稀释度为1：400，37。C1h；应用该方法检测感染金黄色葡萄球菌后的ChIL-6，其结果与本实验室之前应用人的ELISA试剂盒检测的结果相似。结果表明，本试验建立的检测ChlL-6的双抗夹心ELISA方法可用于临床。