气候变化对中国海洋经济可持续发展的影响

为评估气候变化及实施减排政策对中国海洋经济的影响,本文构建了中国海洋经济社会经济核算矩阵(marine social accounting matrix,MSAM),并以此为数据基础构建中国海洋经济可计算一般均衡(computable general equilibrium,CGE)模型,并将该模型与气候变化影响模型相结合,从而实现了从气候变化对自然系统的影响到对经济系统影响的转化。论文设计了实施和不实施温室气体减排两种政策时的可能的6种气候变化情景。各情景的模拟分析表明:海平面上升同时考虑天文潮最高潮位、同时考虑最大台风暴潮和最大天文潮耦合影响两种子情景下,中国实施减排政策对沿海GDP的影响要分别比不实施减排政策低0.19%和0.12%;海平面上升叠加天文潮、风暴潮3种子情景下,实施减排政策对海洋经济的影响要分别比不实施减排政策低1.67%、0.72%、0.37%

The impact of sea-level rise superimposed storm surges on China's ocean economy in 2050

本研究基于ArcGIS的淹没模型与夜光遥感的GDP空间化处理结果,同时结合对2050年中国海洋经济增长预测,评估海平面上升叠加风暴潮三种情景对中; 国沿海各省市海洋经济的影响效应。模拟结果表明:海平面上升叠加风暴潮与天文潮的CHmax-0.3; m情景下全国海洋经济损失最大,2050年损失达到35444.59亿元,占海洋生产总值的9.39%;从2050年各省海洋经济损失比例来看(CHma; x-0.3 m情景),辽宁省损失比例最大,其次为广东省,福建省和广西省;从各省海洋经济损失的绝对值来看,在海平面上升0.3; m的三种情景下,广东、辽宁、江苏、山东均为海洋经济损失绝对值最大的四个省份。To assess the impact of storm surges combined with sea level rise on; China's marine economy, this study utilizes the ArcGIS flood model, the; results of the spatial visualized GDP mapped through luminous space; remote sensing, and the forecast of the growth of China's marine economy; by 2050. We assessed three scenarios of the impact of sea level rise; combined with the effect of storm surge on the marine economies of; China's coastal provinces. The simulation results show:the scenario that; sea level rise combined with storm surges and the CHmax-0.3 m; astronomical tide causes the biggest loss in 2050,which is 3.544459; trillion yuan, accounting for 9.39% of the total output of the marine; economy of China; under the CHmax-0.3 m scenario, in 2050,Liaoning; Province has the largest proportion of losses, followed by; Guangdong,Guangxi and Fujian; under the three scenarios of 0.3 m sea; level rise,Guangdong,Liaoning, Jiangsu,Shandong are the four biggest; provinces in terms of marine economic output losses

An approach to neural control of a class of strict-feedback nonlinear systems

研究一类不确定严反馈非线性系统的跟踪控制问题.通过采用单一神经网络逼近系统的所有未知部分,提出一种新的鲁棒自适应控制设计方法.该方法能直接给出实际控制律和自适应律,有效地解决现有方法中存在的控制设计复杂和计算负担重等问题.稳定性分析表明,闭环系统所有信号是半全局一致最终有界的,并且通过调整控制参数可使跟踪误差任意小.仿真结果验证了所提出方法的有效性.The problem of tracking control is studied for a class of uncertain strict-feedback nonlinear systems.A new robust adaptive control design approach is presented by approximating all the unknown parts of the system with a single neural network.By using this approach,the actual control law and the adaptive law of the controller can be given directly,and the problems,such as control design complexity and high computational burden,are dealt with effectively.The stability analysis shows that the closed-loop system signals are semi-globally uniformly ultimately bounded,and the tracking error can be made arbitrary small by choosing control parameters.Simulation results show the effectiveness of the proposed approach.国家自然科学基金项目(61074017;61074004;61273137;51209026); 辽宁省高等学校优秀人才支持计划项目(2009R06); 中央高校基本科研业务费项目(017004

Study on Determination of Potassium, Sodium, Magnesium, Calcium and Ammonium in Corns by Ion Chromatography

玉米中所含的许多矿物质都是人体重要的营养物质。如钠、钾可以调节细胞和血液的容量;钾还参与蛋白质、碳水化合物的代谢,帮助活化国家自然科学基金资助项目(No.20527005

NMR and Theoretical Study on Interactions between Diperoxovanadate Complex and Substituted Pyridines

为探讨有机配体上取代基团对反应平衡的影响,在模拟生理条件下(0.15mol/L NaCl溶液),应用多核(1H,13C和51V)多维(DOSY)以及变温NMR技术研究双过氧钒配合物[OV(O2)2(D2O)]-/[OV(O2)2(HOD)]-(简写为bpV)与取代吡啶的相互作用.bpV与有机配体的反应性从强到弱的顺序为:皮考林酸根>异烟酸根>异烟酸甲酯>皮考林甲酯,这说明吡啶环上同一位置上的不同取代基团和同一取代基团在不同位置上都影响反应平衡,竞争配位导致一系列新的6配位(配体为异烟酸根和异烟酸甲酯)或7配位(配体为皮考林酸根和皮考林甲酯)的过氧钒物种[OV(O2)2L]n-(L=取代吡啶,n=1或2)生成,密度泛函计算结果较合理地解释了实验结果,并表明溶剂化在反应中起重要作用.To understand the substitution group effects of organic ligands on the reaction equilibrium,the interactions between diperoxovanadate complex [OV(O2)2(D2O)]-/[OV(O2)2(HOD)]-(abbr. bpV) and a series of substituted pyridines were explored using multinuclear(1H,13C,and 51V) magnetic resonance,DOSY,and variable temperature NMR in 0.15 mol/L NaCl ionic medium for mimicking the physiological condition. The reactivity order among the substituted pyridines and bpV is picolinate>isonicotinate> methyl isonicotinate>methyl picolinate. The competitive coordination results in the formation of a series of new six-coordinated(isonicotinate and methyl isonicotinate) or seven-coordinated(picolinate and methyl picolinate) peroxovanadate species [OV(O2)2L]n-(L=substituted pyridines,n=1 or 2). Both the different substitution groups at the same position and the same groups at the different substitution position affect these reactions. The results of density functional calculations provide someway a reasonable explanation for the relative reactivity of the substituted pyridines. Solvation effects play an important role in these reactions.国家自然科学基金(Nos.20772027,20803020);; 973子课题(No.2003CB716005);; 湖南省自然科学基金(No.06JJ30004);; 中国博士后科学基金(No.20070410805);; 湖南省教育厅青年项目(No.06B028);; 固体表面物理化学国家重点实验室资助项目;; 湖南科技大学博士基金(No.E-55107)资助项目

NMR Studies on Interactions between Diperoxovanadate and 1-Ethyl-1H-Imidazole

为探讨过氧钒配合物中有机配体对反应平衡的影响,在模拟生理条件下(0.15MOl·l-1nACl溶液),应用多核(1H、13C和51V)多维(COSy和HSQC)核磁共振(nMr)以及变温技术等谱学方法研究双过氧钒配合物[OV(O2)2l]-(l=d2O或HOd,与之配位的过氧钒物种简写为bPV)和[OV(O2)2ll′]n{-n=1-2,ll′=3-羟基-皮考啉酸根(3-OH-PIC),2-(2′-吡啶)-咪唑(Py-IM),1,10-邻菲啰啉(PHEn),与它们配位的含钒物种分别简写为bPV(3-OH-PIC)、bPV(Py-IM)和bPV(PHEn)}与n-乙基咪唑(n-ET-IM)的相互作用.实验结果表明,n-ET-IM与4种双过氧钒配合物反应性从强到弱的顺序为bPV>bPV(3-OH-PIC)>bPV(Py-IM)>bPV(PHEn).研究表明,金属中心上配体的配位能力、空间位阻和分子量等因素都对反应平衡产生较大的影响,同时竞争配位的结果导致新的6配位过氧物种[OV(O2)2(n-ET-IM)]-的生成.利用上述谱学方法有助于揭示此类相互作用体系的反应过程和配位方式.To understand the effects of organic ligands on the reaction equilibrium, interactions between a series of diperoxovanadate complexes [OV(O2)2L]- (L=D2O or HOD, the corresponding peroxovanadate species (bpV)) and [OV (O2)2LL′]n-{n=1-2; LL′ =3-hydroxyl-picolinate (3-OH-pic), 2-(2′-pyridine)-imidazole (py-im), 1,10-phenanthroline (phen), the corresponding peroxovanadate species bpV(3-OH-pic), bpV(py-im), and bpV(phen)}and 1-ethyl-1H-imidazole (N- Et-im) in solution were explored using multinuclear (1H, 13C, and 51V) magnetic resonance, COSY (correlated spectroscopy), HSQC (heteronuclear single quantum coherence) and variable temperature nuclear magnetic responance (NMR) using 0.15 mol·L-1 NaCl ionic medium to mimic physiological conditions.Experimental results indicated that the reactivity of these four complexes with 1-ethyl-1H-imidazole decreased as follows: bpV>bpV(3-OH-pic)>bpV(py-im)> bpV(phen).The coordinating ability, the steric effect, and the molecular weight of these organic ligands affected the reaction equilibrium.A new six-coordinated peroxovanadate species [OV(O2)2(N-Et-im)]- was formed because of competitive coordination.国家自然科学基金(20772027;20803020);中国博士后科学基金(20070410805);卫生部科学研究基金-福建省卫生教育联合攻关计划(WKJ2008-2-036);厦门市重大疾病攻关研究基金(3502Z20051027)资助项目---

NMR studies on interactions between diperoxovanadate complexes and 1-methylimidazole

To understand the effects of organic ligands of the diperoxovanadate complexes on the reaction equilibrium, the interactions between a series of diperoxovanadate complexes [OV(O-2)(2)LL '](n-) [n=1 similar to 3; LL '=oxalate, abbr. oxa; picolinate, abbr. pic; 2,2 '-bipyridine, abbr. bipy; and 1,10-phenanthroline, abbr. phen. The corresponding peroxovanadate species abbreviate bpV(oxa), bpV(pic), bpV(bipy), and bpV(phen)] and I-methylimidazole (abbr. N-Me-Im) in solution were explored using multinuclear (H-1, C-13, and V-51) magnetic resonance, COSY, and variable temperature NMR in 0.15 mol/L NaCl ionic medium for mimicking the physiological conditions. The experimental results indicated the activity order of these four complexes with I-methylimidazole as follows: bpV(oxa)> bpV(pic)> bpV(bipy)> bpV(phen). Both the coordinating capability and the steric effect of the organic ligands affect the reaction equilibrium. At the same time, a new six-coordinated peroxovanadate species [OV(O-2)(2)(N-Me-Im)](-) is formed due to the competitive coordination

NMR Studies on Interactions between Diperoxovanadate and 1-Ethyl-1H-Imidazole

To understand the effects of organic ligands on the reaction equilibrium, interactions between a series of diperoxovanadate complexes [OV(O-2)(2)L](-) (L=D2O or HOD, the corresponding peroxovanadate species (bpV)) and [OV (O-2)(2)LL'](n-) {n=1-2; LL' =3-hydroxyl-picolinate (3-OH-pic), 2-(2'-pyridine)-imidazole (py-im), 1,10-phenanthroline (phen), the corresponding peroxovanadate species bpV(3-OH-pic), bpV(py-im), and bpV(phen)} and 1-ethyl-1H-imidazole (N-Et-im) in solution were explored using multinuclear (H-1, C-13, and V-51) magnetic resonance, COSY (con-elated spectroscopy), HSQC (heteronuclear single quantum coherence) and variable temperature nuclear magnetic responance (NMR) using 0.15 mol.L-1 NaCl ionic medium to mimic physiological conditions. Experimental results indicated that the reactivity of these four complexes with 1-ethyl-1H-imidazole decreased as follows: bpV > bpV(3-OH-pic)> bpV(py-im)> bpV(phen). The coordinating ability, the steric effect, and the molecular weight of these organic ligands affected the reaction equilibrium. A new six-coordinated peroxovanadate species [OV(O-2)(2)(N-Et-im)](-) was formed because of competitive coordination.National Natural Science Foundation of China [20772027, 20803020]; China Postdoctoral Science Foundation [20070410805]; Science Research Foundation of Ministry of Health & United Fujian Provincial Health ; Education Project for Tackling the Key Research [WKJ2008-2-036]; Health and Science and Technology of Xiamen, China [3502Z20051027

Introducing Glucose Oxidase Gene into RiceMediated by Agrobacterium tumefaciens

过氧化氢（Hydrogen peroxide,H2O2）是植物和病原微生物互作中快速合成的一种早期活性氧类（reactive oxygen species, ROS ），它在植物受到病原微生物侵染后引发的一系列防御反应中起着非常重要的作用，因此通过外源基因导入提高植物体内过氧化氢的含量，可以增强植物的广谱抗病性。葡萄糖氧化酶（glucose oxidase, GO）可以催化β-D-葡萄糖氧化生成过氧化氢和葡萄糖酸，此酶已在数种细菌和真菌中检测到，但在植物和动物中仍未发现。为了尝试将此酶应用于水稻广谱抗病基因工程，本研究将葡萄糖氧化酶基因插入具有潮霉素抗性选择标记的双元载体pCAMBIA1301，新构建为水稻高效表达载体pCAG1301。将此质粒导入根癌农杆菌（Agrobacterium tumefaciens ）菌株LBA4404后,转化粳稻(Oryza sativa )品种日本晴(Nipponbare)成熟胚来源的愈伤组织和幼胚，并由筛选出的潮霉素抗性愈伤组织分化再生植株。对所得到的潮霉素抗性植株的Southern杂交分析表明GO基因已整合到受体基因组,为单拷贝或双拷贝插入。利用过氧化氢与淀粉-碘化钾反应显蓝色的特性检测到了转基因植株产生的过氧化氢，证实GO基因表达产生的葡萄糖氧化酶已经在水稻中发挥功能，这是将GO基因转入单子叶植物的首例报道。 基于过氧化氢诱导的植物防御反应没有种属专一性的优点，可以预期所得转基因水稻植株很可能对水稻的多种病原菌具有良好的抗性。已完成的抗病性鉴定表明，所得转基因水稻植株对稻瘟病具有良好的抗性

基于弹流润滑状态下的非圆齿轮啮合效率研究

在分析非圆齿轮啮合特性及齿廓等啮合角分布规律的基础上，综合考虑相对速度、摩擦因数和油膜厚度等关键因子对啮合功率损失的影响规律，建立了弹流润滑状态下非圆齿轮传动啮合效率数学模型。以非圆齿轮节曲线波谷的轮齿齿顶进入啮合到从波峰的轮齿齿根退出啮合为啮合周期，通过计算啮合角变化下的滑动摩擦和滚动摩擦功率损耗，获得非圆齿轮传动的啮合效率