查询词典 Ms.

Results reveal that the spatial correlation properties of MIMO channel are dependent on the PAS, the antenna pattern and the geometric configuration of the array. When the PASs at the base station and the mobile station are independent, the spatial correlation matrix of the MIMO channel is the Kronecker product of the spatial correlation matrix at the BS and the MS. The temporal correlation properties of the MIMO channel are determined by the PAS at the MS, antenna pattern and the traveling speed of the MS. Based on the analysis of the physical essence, the temporal correlation properties are equivalent to the spatial correlation properties at the MS. The joint spatio-temporal correlation properties at the BS and the MS are quite different. When the PASs at the BS and the MS are independent, the spatial correlation at the BS is independent on the temporal correlation, but this is not true for the spatial correlation at the MS.

分析与计算的结果表明，MIMO信道的空间相关特性由角度谱、阵元的方向图、阵元间距以及阵列几何结构决定，并且当发射端与接收端的空间统计特性相互独立时，MIMO信道的空间相关矩阵可以表示为发射阵列空间相关矩阵与接收阵列空间相关矩阵的Kronecker乘积：信道的时间相关仅与MS端的角度谱、阵元方向图以及MS的运动速度有关，通过对信道时间相关的物理本质的研究，说明了时间相关与MS端空间相关的等价性；MIMO信道的空-时联合相关特性在BS端和MS端具有不同的特点，当发射端与接收端的空间统计特性相互独立时，BS端的空间相关与时间相关是独立的，而由于信道的时间相关与MS端的空间相关具有相同的物理本质，MS端的空间相关与时间相关不是独立的。

Culture tender leaves in culture medium of MS+2,4-D1.5mg/L+30g/L suger+0.7% agar pH5.8 for 20 days in darkness at 25℃, and then subculture to induced Ⅱ-type calli. Use forceps cutting the tissue to nubble with 2mm2, and put the tissue into Agrodacterium tumefaciens LBA4404 liquid supplemented with AS 100mg/L,then, co-culture 3 days, resume 7 days in MS+2,4-D1.5mg/L+30g/L suger+500mg/L cef, take to MS+2,4-D1.5mg/L+30g/L suger+100mg/L cef+10.0mg/L kanamycin culture 20 days in darkness. After that to make it polarize in MS+30g/L suger+100mg/L cef+10.0mg/L km. The percentage of km resistant callus was reached max after infection for 45 min, the average is 29.66%. Simultaneity, tender leave callus are infected 5 min by A. tumefaciens liquid in different negative pressure, and kept on 15 min in Agrodacterium tumefaciens liquid without negative pressure. Then screen out resistant callus and obtain transgenic plants. When the negative pressure is -0.05MP the percentage of km resistant callus was reached max, the average rate is 37.5%.

将心叶接种于MS+2.4-D1.5mg/L+30g/L 蔗糖，琼脂0.7%，pH5.8 培养基中25℃暗培养20d 后继代一次，诱导产生Ⅱ型胚性愈伤组织，用镊子将其夹碎成2mm2大小的小块，置入添加100mg/L AS 的根癌农杆菌LBA4404 菌液中，侵染时间为45min，共培养3 天后，转入MS+2.4-D1.5mg/L+30g/L 蔗糖+500mg/L Cef 培养基中恢复7天，再转入MS+2.4-D1.5mg/L+30g/L 蔗糖+100mg/L Cef+10.0mg/L Km 中，遮光培养20d后，置入其MS+30g/L 蔗糖+100mg/L Cef+10.0mg/L Km 分化，卡那霉素抗性愈伤组织获得率在侵染45min 时达到最大值平均为29.66%；同时以甘蔗心叶愈伤组织材料，通过循环水式真空泵，产生负压，设定不同的负压值，在农杆菌菌液中感染5min 后，在负压条件下继续侵染15min 后，筛选出抗性愈伤组织并获得转化植株，其中在负压为-0.05 时转化率达到最大值，其卡那霉素抗性愈伤组织获得率平均为37.5%。

The LCQ Advantage is the workhorse ion trap mass spectrometer for 你好gh productivity LC/MS/MS results and is easily upgraded to MSn performance. The LCQ Advantage MAX now features the universal Ion Max source that allows simple tool-less switc你好ng of ionization probes. Ion Sweep Gas reduces chemical noise, w你好le a removable ion capillary tube allows for vent free source maintenance. Reliability combined with an easy-to-use interface, makes the LCQ Advantage MAX an ideal match for routine HPLC environment. Library searchable MS/MS spectra add confidence to the identification of analytes present in complex matrices.

LCQ Advantage MAX高效多级离子阱液质联用仪是离子阱光谱阐发平台，可以举行高效液相层析串联质谱LC/MS/MS阐发，而且可以很容易进级到电喷雾离子阱活络度MSnLCQ Advantage MAX高效多级离子阱液质联用仪此刻的首要独特之处是装有通用的Ion Max离子源，无须东西便可简略的调治离子探针，同时离子探针气体吹扫可以削减化学滋扰旌旗灯号可移植离子毛细现象柱无须真空便可养护LCQ Advantage MAX装备不变靠患上住，操做界面简略易用，抱负般配高效液相质谱测试并可检索液相质谱MS/MS库光谱

Among the more than two-dozen new topics are the underlying principles of GC-MS, GC-MS-MS, LC-MS, and ICP-MS, column chromatographic cleanup, gel permeation chromatography, applications to biological sample matrices, matrix solid-phase dispersion, and laboratory-tested experiments.

在超过两打中新题目是GC-MS，GC-MS -MS，LC-MS 和ICP MS 的基础的原则，柱子色谱清除，凝胶渗透色谱学，申请在生物学的标本矩阵，子宫整整阶段的散布和实验室测试的实验。

We studied the optimum medium and hormone combination of callus induction from cotyledons, subculture of callus, shoot regeneration from callus, shoot-extension induction, root induction and identified the chromosome number of the plantlet. The results showed that: MS+2,4-D 2.0mg/L+KT 0.5mg/L, MS���2,4-D 2.5mg/L＋KT 0.5mg/L, MS+2,4-D 0+KT 1.0mg/L, MS+KT 0.5 mg/L and basal MS medium. One plantlet among twenty two was determined as a tetraploidy based on the plant morphology, observation of the leaf stoma and chromosome number of the root, other two plantlets represented morphological variation.

结果表明，诱导章丘大葱子叶产生愈伤组织、愈伤组织的继代培养、愈伤组织芽分化、芽点的伸长及诱导生根的最佳培养基及激素配比分别为：MS+2，4-D 2.0mg/L+KT 0.5mg/L、MS＋2，4-D 2.5mg/L＋KT 0.5mg/L、MS+2，4-D 0+KT 1.0mg/L、MS+KT 0.5mg/L和MS基本培养基；试管苗经驯化移栽后，共有22株成活，成活率为92%，对成活的再生植株进行形态学、叶片气孔及根尖染色体鉴定表明，共有3株发生变异，其中2株为外部形态上的变异，而另一株为染色体的加倍变异。

The results were showed that embryogenic calli were induced from young leaves, which were cultured on MS medium supplemented with 2,4-D 2mg/L and KT 0.2mg/L. For the proliferation of embryogenic calli, the suitable culture medium was MS+BA 8mg/L +NAA 1mg/L. The development and maturation of somatic embryo could be much improved by using the medium of MS+ZT 2mg/L or BA 5mg/L +IAA 0.2mg/L. For the induction of secondary somatic embryo from integral somatic embryo, the suitable culture medium was MS+KT 0.1mg/L+NAA 0.01 mg/L or MS+ZT 0.1mg/L+NAA 0.01 mg/L, the proliferation frequency is 214%, 256% respectively. The cotyledonary generated from somatic embryos of Aesculus hippocastanum L.

本文就欧洲七叶树的组织培养和体细胞胚发生以及植株再生进行了系统研究，主要结果如下：以植物细胞具有全能性的理论为依据，以欧洲七叶树幼嫩叶片为外植体，进行体细胞胚胎发生研究，研究结果表明，诱导愈伤组织的适宜培养基是MS+2，4-D 2mg／L+KT0.2mg／L，MS+BA 8mg／L+NAA 1mg／L有利于胚性愈伤组织的诱导和增殖，添加ZT 2mg／L或BA 5mg／L和IAA 0.2mg／L的MS培养基有利于体细胞胚发育和成熟，体细胞胚可直接诱导次生胚发生，MS+KT 0.1mg／L+NAA 0.01 mg／L或MS+ZT 0.1mg／L+NAA 0.01 mg／L培养基诱导效果最好，增殖频率分别为214％、256％。

The germination test of Sporocarps of Microlepia hancei prantl had been done, the callus can be induced from the delicate stem of Microlepia hancei prantl; The inducement and proliferation medium of callus was MS���6-BA2 mg/L+NAA0.2 mg/L;the optimal combination of hormones of buds differentiation was MS+6-BA 0.4 mg/L; the effect of MS medium in radication culture was better than 1/2MS, the roots of plants were all efficiently induced in MS medium without reference to adding IBA、NAA or IBA＋NAA, the rate of radication was high; the effect of seedling cultured in the mixture of perlite and turf soil was better than perlite、garden soil and river sands.the mixture of perlite and turf soil has the excellences such as ventilate、water conservation 、nourishment and so on,the survival rate was higher and seedling substance was also hale.

试验进行了华南鳞盖蕨孢子果的萌发试验，并利用幼嫩茎段进行诱导愈伤组织；愈伤组织的诱导与增殖培养基为MS＋6-BA2 mg/L+NAA0.2 mg/L；其芽分化最佳激素组合为MS+6-BA 0.4 mg/L；生根培养中MS基本培养基比1/2MS效果好，MS基本培养基不论附加生长素IBA、NAA或IBA＋NAA，均能有效地诱导植株生根，生根率高；假植以珍珠岩和泥炭土的混合物为基质效果优于珍珠岩、菜园土和河沙，具有通气、保水、营养等优点，假植成活率高，苗势健壮。

The experimental results shows, if the ratio between MS-1 and OP-10 rangs from 1:1 to 3:l,and the total dosage of them is about 20% of Octamethylcyclotetrasiloxane (D4 ) in quality, we can obtain a kind of stable seeded emulsion of organic silicone modified acrylic ester emulsion. At the same time, if the ratio between MS-1 and Tetramethylammonium Chlorideis l:1.7,the total dosage is about 50% of D4 in quality; the ratio between MS-1 and Cetyltrimethylammonium Chlorineis 7:1, the total dosage is about 25% of D4 in quality,we can also obtain stable seeded emulsions. But if the complex emulsifier system is made of TMAC and OP-10, MS-1 and Peregal O or CTAC and Span-80, we can not synthesize any kind of satisfactory seeded emulsions.

实验结果表明：当MS-1与OP-10的质量比为1：1～3：1，总用量为八甲基环四硅氧烷(D_4)的20％左右时，可合成稳定性良好的硅丙种子乳液；MS-1与四甲基氯化铵的质量比为1：1.7，总用量为D_4的50％左右，MS-1与十六烷基三甲基氯化铵的质量比为7：1，总用量为D_4的25％左右时，亦能得到稳定的硅丙种子乳液；而TMAC与OP-10、MS-1与Peregal O以及CTAC与Span-80的复合体系作为乳化剂时均不能得到满意的硅丙种子乳液。

Based on present experimental formulae to calculate martensite starting temperature Ms of various steel grades, with analysis on the effect of alloying elements on Ms of steel, the experiential formula Ms = 550-330C-35Mn-17Ni-12Cr-21Mo-10Cu-5W-10Si-0Ti+10Co+30Al for maraging stainless steel is given in this paper.

本文依据马氏体时效不锈钢的化学成分及实测Ms温度，利用现有的Ms温度计算公式进行分析计算，提出新的马氏体时效不锈钢的Ms温度计算公式。1 现有Ms温度经验计算公式的分析影响钢的Ms点的因素很多，如化学成分、淬火冷却速度、奥氏体化条件、形变等[2 ] 。

The research on the tissue culture and cell suspension culture showed that thesuitable culture medium for inducing bud was MS supplemented with 1.5mg/L 6-BAand 0.1mg/L NAA, and for the generation-continuing multiplication was MSsupplemented with 1.5mg/L 6-BA and 0.2mg/L NAA. The rooting medium was1/2MS supplemented with 0.5mg/L IBA and the rooting rate was 45.0%. Plantletsurvival after transfer to sand was 52.5%.The induction rate of calli was66.7%～86.6% and the optimum medium was MS medium with 0.5mg/L 6-BA and2.0mg/L 2,4-D. The calli became smallest partical size, friable and had gooddispersion ability after 3 times successive transfer culture, the optimum medium wasMS medium with 0.2mg/L 6-BA and 2.0mg/L 2,4-D. Culturing these particles on sixkinds of MS liquid media with different hormone contents, the optimum medium wasselected basing on he change of the density of single-cell, the density of cellaggrefate and the mass of cell.

对蒜头果进行的组织培养与细胞悬浮培养研究结果表明：MS+6-BA1.5mg／L+NAA0.1mg／L+蔗糖3％激素组合能够较好地诱导芽的初始分化和增殖，适宜的芽苗继代增殖培养基为MS+6-BA1.5mg／L+NAA0.2mg／L+蔗糖3％；采用1／2MS+IBA0.5mg／L+蔗糖3％为生根培养基，生根率为45.0％；移栽到河沙的生根苗成活率为52.5％；愈伤组织诱导率为66.7％～86.6％，其中以MS+6-BA0.5mg／L+2，4-D2.0mg／L+蔗糖3％的培养基最佳，其诱导出的愈伤组织具有较强的增殖能力和较好的脆散结构，最佳继代培养基为MS+6-BA0.2mg／L+2，4-D2.0mg／L+蔗糖3％，且培养基中的6-BA与2，4-D浓度的比值越小，愈伤组织生长越快，结构越脆散，增殖率越高；将继代后的愈伤组织转入6种含不同激素浓度组合的MS液体培养基中进行振荡培养，在综合分析各培养基的单细胞密度，细胞团块密度，细胞生物量增长率等指标后，初步筛选出MS+6-BA0.2mg／L+2，4-D2.0mg／L培养基为较好的液体培养基。

Neither the killing of Mr Zarqawi nor any breakthrough on the political front will stop the insurgency and the fratricidal murders in their tracks.

在对危险的南部地区访问时，他斥责什叶派民兵领导人对中央集权的挑衅行为。

In fact,I've got him on the satellite mobile right now.

实际上 我们已接通卫星可视电话了