Rates, polarizations, and asymmetries in charmless vector-vector B meson decays

With a sample of approximately 89 x 10(6) B(-)B pairs collected with the BABAR detector, we perform a search for B meson decays into pairs of charmless vector mesons (phi, rho, and K*). We measure the branching fractions, determine the degree of longitudinal polarization, and search for CP violation asymmetries in the processes B+-->phiK(*+), B0-->phiK(*0), B+-->rho(0)K(*+), and B+-->rho(0)rho(+). We also set an upper limit on the branching fraction for the decay B0-->rho(0)rho(0).     

Measurements of the branching fractions and bounds on the charge asymmetries of charmless three-body charged B decays

We present measurements of branching fractions and charge asymmetries for charmless B-meson decays to three-body final states of charged pions and kaons. The analysis uses 81.8 fb(-1) of data collected at the Upsilon(4S) resonance with the BABAR detector at the SLAC PEP-II asymmetric B Factory. We measure the branching fractions B(B+-->pi(+)pi(-)pi(+))=(10.9+/-3.3+/-1.6)x10(-6), B(B+-->K+pi(-)pi(+))=(59.1+/-3.8+/-3.2)x10(-6), and B(B+-->K+K-K+)=(29.6+/-2.1+/-1.6)x10(-6) and provide 90% C.L. upper limits for other decays. We observe no charge asymmetries for these modes.     

Observation of B+-->a1+(1260)K0 and B0-->a1-(1260)K+

We present branching fraction measurements of the decays B(+)-->a(1)(+)(1260)K(0) and B(0)-->a(1)(-)(1260)K(+) with a(1)(+/-)(1260)-->pi(-/+)pi(+/-)pi(+/-). The data sample corresponds to 383 x 10(6) BB pairs produced in e(+)e(-) annihilation through the Upsilon(4S) resonance. We measure the products of the branching fractions B(B(+)-->a(1)(+)(1260)K(0)B(a(1)(+)(1260)-->pi(-)pi(+)pi(+))=(17.4+/-2.5+/-2.2) x 10(-6) and B(B(0)-->a(1)(-)(1260)K(+)B(a(1)(-)(1260)-->pi(+)pi(-)pi(-)) = (8.2+/-1.5+/-1.2) x 10(-6). We also measure the charge asymmetries A(ch)(B(+)-->a(1)(+)(1260)K(0) = 0.12+/-0.11+/-0.02 and A(ch)(B(0)-->a(1)(-)(1260)K+) = -0.16+/-0.12+/-0.01. The first uncertainty quoted is statistical and the second is systematic.     

Evidence for CP violation in B0-->J/psipi0 decays

We present measurements of the branching fraction and time-dependent CP asymmetries in B0-->J/psipi0 decays based on 466 x 10(6) Upsilon(4S)-->BB over events collected with the BABAR detector at the SLAC PEP-II asymmetric-energy B factory. We measure the CP asymmetry parameters S= -1.23+/-0.21(stat)+/-0.04(syst) and C= -0.20+/-0.19(stat)+/-0.03(syst), where the measured value of (S, C) is 4.0 standard deviations from (0, 0) including systematic uncertainties. The branching fraction is determined to be B(B0-->J/psipi0)=[1.69+/-0.14(stat)+/-0.07(syst)]x10(-5).     

Uncertainty resulting from inconstancy in the slope of the log plot of homologous series

Summary The free energy of partition of a methylene group is constant within a homologous series down to C₅ and nearly constant to C₃, contrary to the finding of Golovnya and Grigoryeva [5]. Retention indices are linear with carbon number: values may be extrapolated from higher carbon numbers to C₅ within experimental uncertainty, to C₄ with error no greater than 5 units and to C₃ with error no greater than 10 units. Error in extrapolating the logarithm of the adjusted retention time, log t_R, to C₅ is thus negligible, to C₄ has possible error up to 5b/100 and to C₃ up to 10b/100, whereb is the slope of the plot of log t_R against carbon number.     

Rapid determination of the neurotoxin lolitrem B in perennial ryegrass by high-performance liquid chromatography with fluorescence detection

A rapid, sensitive and quantitative method, based on high-performance liquid chromatography with fluorescence detection, is described for the determination of the neurotoxin lolitrem B in perennial ryegrass, in the ppm to sub-ppm range. The method, which requires a minimal clean-up step prior to chromatographic analysis, is suitable for the routine analysis of large numbers of ryegrass samples, and is currently being used in New Zealand to study the livestock disorder ryegrass staggers. The method is suitable for determining lolitrem B in the whole plant, the seed, and dissected plant components.