高光谱影像的鲜桃可溶性固形物含量预测模型

可溶性固形物含量(SSC)是决定鲜桃风味和品质的重要成分。高光谱影像的特征提取为无损检测可溶性固形物含量提供了数据基础和方法路径。先前的研究表明,基于多光谱、荧光谱、近红外光谱、电子鼻的水果内部品质评估取得较好的结果。但是,由于缺少多特征融合,从而限制了水果品质的精准估测。为此,提出了一种基于堆栈自动编码器-粒子群优化支持向量回归(SAE-PSO-SVR)模型预测鲜桃可溶性固形物含量。首先,利用高光谱影像提取光谱信息、空间信息及空-谱融合信息。其次,设置普适性堆栈自动编码器(SAE)提取光谱信息、空间信息及空-谱融合信息的深层特征。最后,将深层特征作为粒子群优化支持向量回归(PSO-SVR)模型的输入数据进行鲜桃可溶性固形物含量的预测。其中,对于光谱信息作为输入的SAE模型,设计了453-300-200-100-40, 453-350-250-150-50, 453-350-250-100-60的三个隐含层结构。对于空间信息作为输入的SAE模型,设计了894-700-500-300-50, 894-650-350-200-80, 894-800-700-500-100的三个隐含层结构。对于融合信息作为输入的SAE模型,设计了1347-800-400-200-40, 1347-750-550-400-100, 1347-700-500-360-150的三个隐含层结构。实验结果表明,对于输入数据分别为光谱信息、空间信息及融合信息的SAE模型,结构为453-300-200-100-40, 894-800-700-500-100和1347-750-550-400-100的模型效果较好,而且基于融合信息的模型预测精度明显优于基于光谱信息或者图像信息的模型。为了验证模型的普适性,利用结构为1347-750-550-400-100的SAE模型提取融合信息的深层特征估测不同品种鲜桃的可溶性固形物含量并进行可视化。结果表明,基于结构为1237-650-310-130的SAE-PSO-SVR模型预测效果最好(R2=0.873 3, RMSE=0.645 1)。因此,所提出的SAE-PSO-SVR模型提高了鲜桃可溶性固形物含量的估计精度,为鲜桃的其他成分检测提供了技术支撑。     

Observation of B Meson decays to b1pi and b1K

We present the results of searches for decays of B mesons to final states with a b1 meson and a charged pion or kaon. The data, collected with the BABAR detector at the Stanford Linear Accelerator Center, represent 382x10(6) BB[over ] pairs produced in e+e- annihilation. The results for the branching fractions are, in units of 10(-6), B(B+-->b1(0)pi+)=6.7+/-1.7+/-1.0, B(B+-->b1(0)K+)=9.1+/-1.7+/-1.0, B(B0-->b1(-/+)pi(+/-))=10.9+/-1.2+/-0.9, and B(B0-->b1(-)K+)=7.4+/-1.0+/-1.0, with the assumption that B(b1-->omega pi)=1. We also measure charge and flavor asymmetries A(ch)(B+-->b1(0)pi+)=0.05+/-0.16+/-0.02, Ach(B+-->b1(0)K+)=-0.46+/-0.20+/-0.02, A(ch)(B0-->b1(-/+)pi(+/-))=-0.05+/-0.10+/-0.02, C(B0-->b1(-/+)pi(+/-))=-0.22+/-0.23+/-0.05, DeltaC(B0-->b1(-/+)pi(+/-))=-1.04+/-0.23+/-0.08, and A(ch)(B0-->b1(-)K+)=-0.07+/-0.12+/-0.02. The first error quoted is statistical, and the second systematic.     

Structure of Rb-III: novel modulated stacking structures in alkali metals

The crystal structure of Rb-III, stable between 13 and 17 GPa, has been determined from quasi-single-crystal x-ray diffraction data. It is orthorhombic, space group C222(1), with 52 atoms in the unit cell, and has an 8-10-8-8-10-8 stacking of 8- and 10-atom layers. The recently reported 84-atom structure of Cs-III can be understood as an 8-8-10-8-8-8-8-10-8-8 stacking of the same layers. These represent a new class of modulated elemental structures.     

Exclusive branching-fraction measurements of semileptonic tau decays into three charged hadrons, into phipi(-)nu tau, and into phi K(-)nu tau

Using a data sample corresponding to an integrated luminosity of 342 fb(-1) collected with the BABAR detector at the SLAC PEP-II electron-positron storage ring operating at a center-of-mass energy near 10.58 GeV, we measure B(tau(-)--> pi(-)pi(-)pi+nu(tau)(ex.K(S0))=(8.83+/-0.01+/-0.13)%, B(tau(-) -->K(-)pi(-)pi+nu tau(ex.K(S0))=(0.273+/-0.002+/-0.009)%, B(tau(-) -->K(-)pi(-)K+nu tau)=(0.1346+/-0.0010+/-0.0036)%, and B(tau(-) -->K(-)K(-)K+nu tau)=(1.58+/-0.13+/-0.12)x10;{-5}, where the uncertainties are statistical and systematic, respectively. These include significant improvements over previous measurements and a first measurement of B(tau(-) -->K(-)K(-)K+nu tau) in which no resonance structure is assumed. We also report a first measurement of B(tau(-) -->var phi(-)nu tau)=(3.42+/-0.55+/-0.25)x10(-5), a new measurement of B(tau(-) -->var phi K(-)nu tau)=(3.39+/-0.20+/-0.28)x10(-5) and a first upper limit on B(tau(-) -->K(-)K(-)K+nu tau(ex.var phi)).     

Measurement of the branching fraction,and bounds on the CP-violating asymmetries,of neutral B decays to D*+/- D-/+

We present measurements of the branching fraction and CP-violating asymmetries for neutral B decays to D(*+/-)D-/+. The measurement uses a data sample of approximately 88x10(6) Upsilon(4S)-->BBmacr; decays collected with the BABAR detector at the SLAC PEP-II asymmetric-energy e(+)-e(-) collider. By fully reconstructing the D(*+/-)D-/+ decay products, we measure the branching fraction to be (8.8+/-1.0+/-1.3)x10(-4) and the time-integrated CP-violating asymmetry between the rates to D(*-)D+ and D(*+)D- to be A=-0.03+/-0.11+/-0.05. We also measure the time-dependent CP-violating asymmetry parameters to be S(-+)=-0.24+/-0.69+/-0.12, C(-+)=-0.22+/-0.37+/-0.10 for B-->D(*-)D+ and S(+-)=-0.82+/-0.75+/-0.14, C(+-)=-0.47+/-0.40+/-0.12 for B-->D(*+)D-. In each case, the first error is statistical and the second error is systematic.     

Measurement of CP-violating asymmetries in B0-->D*(+/-)D(-/+)

We present updated measurements of CP-violating asymmetries in the decays B0-->D*(+/-)D(-/+) and B0-->D+D- using (383+/-4) x 10(6)B(B) pairs collected by the BABAR detector at the SLAC PEP-II B factory. We determine the time-integrated CP asymmetry A(D*(+/-)D(-/+))=0.12+/-0.06+/-0.02, and the time-dependent asymmetry parameters to be C(D*+D-)=0.18+/-0.15+/-0.04, S(D*+D-)=-0.79+/-0.21+/-0.06, C(D*-D+)=0.23+/-0.15+/-0.04, S(D*-D+)=-0.44+/-0.22+/-0.06, C(D+D-)=0.11+/-0.22+/-0.07, and S(D+D-)=-0.54+/-0.34+/-0.06, where the first uncertainty is statistical and the second is systematic.     

Muon decay: measurement of the transverse polarization of the decay positrons and its implications for the fermi coupling constant and time reversal invariance

The two transverse polarization components P(T1) and P(T2) of the e(+) from the decay of polarized mu(+) have been measured as a function of the e(+) energy. Their energy averaged values are P(T1)=(6.3+/-7.7+/-3.4) x 10(-3) and P(T2)=(-3.7+/-7.7+/-3.4) x 10(-3). From the energy dependence of P(T1) and P(T2) the decay parameters eta,eta(') and alpha(')/A,beta(')/A are derived, respectively. Assuming only one additional coupling besides the dominant V-A interaction one gets improved limits on eta, beta(')/A, and the scalar coupling constant g(S)(RR): eta=(-2.1+/-7.0+/-1.0) x 10(-3), beta(')/A=(-1.3+/-3.5+/-0.6) x 10(-3), Re{g(S)(RR)}=(-4.2+/-14.0+/-2.0) x 10(-3), and Im{g(S)(RR)}=(5.2+/-14.0+/-2.4) x 10(-3).     

稀土氟碳酸盐矿物的拉曼光谱研究

研究了氟碳钡铈矿Ｃｅ２Ｂａ［ＣＯ３］３Ｆ２、氟碳钙铈矿Ｃｅ２Ｃａ［ＣＯ３］３Ｆ２和氟碳铈矿Ｃｅ［ＣＯ３］２Ｆ等矿物的拉曼光谱特征。结果表明,钡稀土氟碳酸盐矿物（氟碳钡铈矿、氟碳铈钡矿、黄河矿）的Ｒａｍａｎ光谱特点是,ν１和ν２为单峰值,ν３和ν４为双峰值。钙稀土氟碳酸盐矿物（氟碳钙铈矿）的拉曼光谱带中ν１和ν４为双峰值,ν２和ν３为单峰值。稀土氟碳酸盐矿物（氟碳铈矿）的Ｒａｍａｎ光谱的特点是,ν１、ν２和ν４为单峰值,ν３为双峰值。     

三苯胺衍生物分子非线性光学性质的理论研究

在密度泛函理论水平上,利用响应函数方法,研究了1-{(1E)-2-[4-(二苯胺基)苯基]乙烯基}-4-[4-N,N-二甲胺]苯(PVMB)和1-[(1E)-2-(4-(1E)-2-{4-[4-N,N-二甲胺]苯基}乙烯基)苯基]苯胺}苯基)乙烯基]-4-[4-N,N-二甲胺]苯(DPVMB)两分子的双光子吸收特性.计算结果表明,这两个化合物都具有较好的双光子吸收特性,且具有两分支结构的DPVMB分子比具有单支结构的PVMB分子有更强的双光子吸收强度.计算数值结果和实验结果符合地较好.     

Observation of B0-->omega K0, B+-->eta pi+, and B+-->eta K+ and study of related decays

We present measurements of branching fractions and charge asymmetries for seven B-meson decays with an eta, eta', or omega meson in the final state. The data sample corresponds to 89x10(6) BB pairs produced from e(+)e(-) annihilation at the Upsilon(4S) resonance. We measure the following branching fractions in units of 10(-6): B(B+-->eta pi(+))=5.3+/-1.0+/-0.3, B(B+-->eta K+)=3.4+/-0.8+/-0.2, B(B0-->eta K0)=2.9+/-1.0+/-0.2 (<5.2, 90% C.L.), B(B+-->eta(')pi(+))=2.7+/-1.2+/-0.3 (<4.5, 90% C.L.), B(B+-->omega pi(+))=5.5+/-0.9+/-0.5, B(B+-->omega K+)=4.8+/-0.8+/-0.4, and B(B0-->omega K0)=5.9(+1.6)(-1.3)+/-0.5. The charge asymmetries are A(ch)(B+-->eta pi(+))=-0.44+/-0.18+/-0.01, A(ch)(B+-->eta K+)=-0.52+/-0.24+/-0.01, A(ch)(B+-->omega pi(+))=0.03+/-0.16+/-0.01, and A(ch)(B+-->omega K+)=-0.09+/-0.17+/-0.01.     

Measurements of the branching fractions for psi(3770)-->D(0)D[over ](0), D+D-, DD[over ], and the resonance parameters of psi(3770) and psi(2S)

We measure the branching fractions for psi(3770)-->D(0)D[over ](0), D+D-, DD[over ], and non-DD[over ] to be (46.7+/-4.7+/-2.3)%, (36.9+/-3.7+/-2.8)%, (83.6+/-7.3+/-4.2)%, and (16.4+/-7.3+/-4.2)%, respectively. The resonance parameters of psi(3770) and psi(2S) are measured to be M_(psi(3770))=3772.2+/-0.7+/-0.3 MeV, Gamma_(psi(3770))(tot)=26.9+/-2.4+/-0.3 MeV, and Gamma_(psi(3770))(ee)=251+/-26+/-11 eV; M_(psi(2S))=3685.5+/-0.0+/-0.3 MeV, Gamma_(psi(2S))(tot)=331+/-58+/-2 keV, and Gamma_(psi(2S))(ee)=2.330+/-0.036+/-0.110 keV. We also measure the light hadron R value to be R(uds)=2.262+/-0.054+/-0.109 in the energy region from 3.660 to 3.872 GeV.     

Measurements of branching fractions and CP-violating asymmetries in B0-->rho(+/-)h(-/+) decays

We present measurements of branching fractions and CP-violating asymmetries in B0-->rho(+/-)pi(-/+) and B0-->rho-K+ decays. The results are obtained from a data sample of 88.9 x 10(6) Upsilon(4S)-->BB decays collected with the BABAR detector at the SLAC PEP-II asymmetric-energy B Factory. From a time-dependent maximum likelihood fit we measure the branching fractions B(B0-->rho(+/-)pi(-/+))=[22.6+/-1.8 (stat)+/-2.2 (syst)]x10(-6) and B(B0-->rho-K+)=(7.3 -1.2( +1.3)+/-1.3)x10(-6), and the CP-violating charge asymmetries A(rhopi)(CP)=-0.18+/-0.08+/-0.03 and A(rhoK)(CP)=0.28+/-0.17+/-0.08, the direct CP violation parameter C(rhopi)=0.36+/-0.18+/-0.04 and the mixing-induced CP violation parameter S(rhopi)=0.19+/-0.24+/-0.03, and the dilution parameters DeltaC(rhopi)=0.28 -0.19( +0.18)+/-0.04 and DeltaS(rhopi)=0.15+/-0.25+/-0.03.     

Measurement of time-dependent CP asymmetries in B0-->D(*)+/-D+/- decays

We present a first measurement of CP asymmetries in neutral B decays to D+D-, and updated CP asymmetry measurements in decays to D(*+)D- and D(*-)D+. We use fully reconstructed decays collected in a data sample of (232+/-3) x 10(6) gamma(4S)-->BB events in the BABAR detector at the PEP-II asymmetric-energy B Factory at SLAC. We determine the time-dependent asymmetry parameters to be SD(*+)(D-)=-0.54+/-0.35+/-0.07, CD(*+)(D-)=0.09+/-0.25+/-0.06, SD(*-)(D+)=-0.29+/-0.33+/-0.07, CD(*-)(D+)=0.17+/-0.24+/-0.04, SD+(D-)=-0.29+/-0.63+/-0.06, and CD+(D-)=0.11+/-0.35+/-0.06, where in each case the first error is statistical and the second error is systematic.     

Observation and polarization measurements of B+/- -->phiK1 +/- and B +/- -->phiK2 *+/-

With the full BABAR data sample of 465 x 10(6) B(over)B pairs, we observe the decays B+/- -->phiK_(1)(1270) +/- and B +/- -->phiK*_(2)(1430)+/-. We measure the branching fractions (6.1+/-1.6+/-1.1) x 10(-6) and (8.4+/-1.8+/-1.0) x 10(-6) and the fractions of longitudinal polarization 0.46 (+0.12+0.06) _(-0.13-0.07) and 0.80(+0.09)_(-0.10)+/-0.03, respectively. We also report on the B+/- -->phiK*_(0)(1430)+/- decay branching fraction of (7.0+/-1.3+/-0.9) x 10(-6) and several parameters sensitive to CP violation and interference in the above three decays. Upper limits are placed on the B+/- decay rates to final states with phi and K_1(1400)+/-, K*(1410)+/-, K2(1770)+/-, or K_2(1820)+/-. Understanding the observed polarization pattern requires amplitude contributions from an uncertain source.     

2,2-二甲基-3-(2,2-二氯乙烯基)环丙烷羧酸乙(甲)酯及其合成中间体的结构测定

由异戊烯醇-原乙酸三乙（甲）酯法相继合成了拟除虫菊酯类农药中间体3，3-二甲基-4-戊烯酸乙（甲）酯，4，6，6，6-四氯-3，3-二甲基己酸乙（甲）酯和2，2-二甲基-3－（2，2-二氯乙烯基）环丙烷羧酸乙（甲）酯等化合物，对这些化合物进行了元素分析、红外光谱、1HNMR等测定，与文献结果相符，为了进一步明确结构，测定了未见报道的13CNMR，给出了波谱数据归属．     

胺基化合物修饰戊二醛交联壳聚糖树脂的合成及其红外光谱研究

研究了以三聚氯氰为活化剂,正丁胺、二甲胺、三甲胺、三乙胺、苯甲胺、对甲基苯胺、对氨基苯磺酸修饰戊二醛交联壳聚糖的制备及其红外光谱。壳聚糖1 155 cm-1的糖苷键ν_(C—O—C)吸收峰、899 cm-1的环振动吸收峰和1 030 cm-1的伯羟基ν_(C—OH)吸收峰基本不变。在3 430～3 440 cm-1的ν_(O—H)和ν_(N—H)吸收峰稍有变化,1 400～1 384 cm-1的δ_(C—H)吸收峰变化较明显。氨基化修饰交联壳聚糖仲羟基的ν_(C—OH)吸收峰由1 095 cm-1移至1 060～1 070 cm-1。三聚氯氰活化交联壳聚糖在803～812 cm-1和1 584～1 590 cm-1出现均三嗪环骨架振动吸收峰。随取代度和脱乙酰度不同,壳聚糖的酰胺Ⅰ,Ⅱ,Ⅲ峰强度变化明显。伯仲胺修饰交联壳聚糖在1 517～1 530 cm-1出现质子化氨基δ_(N—H)吸收峰,三甲胺、三乙胺修饰交联壳聚糖此峰消失或减弱,但在1 400～1 500 cm-1出现一组ν_(C—N)吸收峰。     

季铵盐型双子表面活性剂在空气-水界面的单分子膜

利用Langmuir膜天平测定不对称双子表面活性剂12-2-16和对称双子表面活性剂12-2-12在空气-水界面上形成单分子膜的表面压,通过单分子膜的π-A等温线、微分等温线和静态弹性,分析其相转变和成膜特性.结果表明,与传统阳离子表面活性剂DTAB比较,12-2-16、12-2-12比DTAB单分子膜的分子极限面积大,崩溃压高,并有较高的静态弹性,因而具有较高的凝聚性和稳定性,其中12-2-16单分子膜的凝聚性和稳定性最高.     

First observation of the decays B(0) → D(+)K(-)π(+)π(-) and B(-) → D(0)K(-)π(+)π(-)

First observations of the Cabibbo-suppressed decays B(0) → D(+)K(-)π(+)π(-) and B(-) → D(0)K(-)π(+)π(-) are reported using 35 pb(-1) of data collected with the LHCb detector. Their branching fractions are measured with respect to the corresponding Cabibbo-favored decays, from which we obtain B(B(0) → D(+)K(-)π(+)π(-))/B(B(0) → D(+)π(-)π(+)π(-))=(5.9±1.1±0.5)×10(-2) and B(B(-) → D(0)K(-)π(+)π(-))/B(B(-) → D(0)π(-)π(+)π(-))=(9.4±1.3±0.9)×10(-2), where the uncertainties are statistical and systematic, respectively. The B(-) → D(0)K(-)π(+)π(-) decay is particularly interesting, as it can be used in a similar way to B(-) → D(0)K(-) to measure the Cabibbo-Kobayashi-Maskawa phase γ.     

Structural complexity in gallium under high pressure: relation to alkali elements

Ga-II, the stable phase of Ga between 2 and 10 GPa at room temperature, is shown to have a complex 104-atom orthorhombic structure. A new phase, Ga-V, is found between 10 and 14 GPa, with a rhombohedral hR6 structure. Ga-II has a modulated layer structure like those recently reported for Rb-III and Cs-III, with similar 8- and 10-atom a-b layers stacked along the c axis in the sequence 8-10-8-8-10-8-8-10-8-8-10-8. The cI16 structure of Li and Na can be understood as a stacking of very similar 8-atom layers. It is suggested that a Hume-Rothery mechanism contributes to the occurrence of these complex structures in such different metals.     

Observation of B+/- -->omegaK+/- decay

We report the first observation of the charmless two-body mode B+/--->omegaK+/- decay, and a new measurement of the branching fraction for the B+/--->omegapi(+/-) decay. The measured branching fractions are B(B+/--->omegaK+/-)=(9.2(+2.6)(-2.3)+/-1.0)x10(-6) and B(B+/--->omegapi(+/-))=(4.2(+2.0)(-1.8)+/-0.5)x10(-6). We also measure the partial rate asymmetry of B+/--->omegaK+/- decays and obtain A(CP)=-0.21+/-0.28+/-0.03. The results are based on a data sample of 29.4 fb(-1) collected on the Upsilon(4S) resonance by the Belle detector at the KEKB e(+)e(-) collider.