Measurement of the Lifetime of the Metastable 5d\u3csub\u3e3/2\u3c/sub\u3e26d\u3csub\u3e3/2\u3c/sub\u3e, J=0 Autoionizing State of Barium

We report a measurement of the lifetime of the metastable 5d3/226d3/2, J=0 autoionizing state of barium. We have determined the lifetime to be 190(10) ns

Two-Step Stabilization of Autoionizing States

A two-step process using internal conversion and fluorescence to stabilize the 6P3/211d autoionizing state of barium has been observed. The internal conversion produces very highly excited autoionizing Rydberg states, which then emit fluorescence to produce singly excited, bound states. Inclusion of this process should bring calculations closer to agreement with recent measurements of dielectronic recombination

Ovalbumin sensitization and challenge increases the number of lung cells possessing a mesenchymal stromal cell phenotype

Abstract Background Recent studies have indicated the presence of multipotent mesenchymal stromal cells (MSCs) in human lung diseases. Excess airway smooth muscle, myofibroblasts and activated fibroblasts have each been noted in asthma, suggesting that mesenchymal progenitor cells play a role in asthma pathogenesis. We therefore sought to determine whether MSCs are present in the lungs of ovalbumin (OVA)-sensitized and challenged mice, a model of allergic airways disease. Methods Balb/c mice were sensitized and challenged with PBS or OVA over a 25 day period. Flow cytometry as well as colony forming and differentiation potential were used to analyze the emergence of MSCs along with gene expression studies using immunochemical analyses, quantitative polymerase chain reaction (qPCR), and gene expression beadchips. Results A CD45-negative subset of cells expressed Stro-1, Sca-1, CD73 and CD105. Selection for these markers and negative selection against CD45 yielded a population of cells capable of adipogenic, osteogenic and chondrogenic differentiation. Lungs from OVA-treated mice demonstrated a greater average colony forming unit-fibroblast (CFU-F) than control mice. Sorted cells differed from unsorted lung adherent cells, exhibiting a pattern of gene expression nearly identical to bone marrow-derived sorted cells. Finally, cells isolated from the bronchoalveolar lavage of a human asthma patient showed identical patterns of cell surface markers and differentiation potential. Conclusions In summary, allergen sensitization and challenge is accompanied by an increase of MSCs resident in the lungs that may regulate inflammatory and fibrotic responses.http://deepblue.lib.umich.edu/bitstream/2027.42/78265/1/1465-9921-11-127.xmlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78265/2/1465-9921-11-127.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/78265/3/1465-9921-11-127-S1.DOCPeer Reviewe

Stability of rotating states in a weakly-interacting Bose-Einstein condensate

We investigate the lowest state of a rotating, weakly-interacting Bose-Einstein condensate trapped in a harmonic confining potential that is driven by an infinitesimally asymmetric perturbation. Although in an axially-symmetric confining potential the gas has an axially-symmetric single-particle density distribution, we show that in the presence of the small asymmetric perturbation its lowest state is the one given by the mean-field approximation, which is a broken-symmetric state. We also estimate the rate of relaxation of angular momentum when the gas is no longer driven by the asymmetric perturbation and identify two regimes of "slow" and "fast" relaxation. States of certain symmetry are found to be more robust.Comment: 6 pages, RevTe

Vortex stabilization in a small rotating asymmetric Bose-Einstein condensate

We use a variational method to investigate the ground-state phase diagram of a small, asymmetric Bose-Einstein condensate with respect to the dimensionless interparticle interaction strength $\gamma$ and the applied external rotation speed $\Omega$. For a given $\gamma$, the transition lines between no-vortex and vortex states are shifted toward higher $\Omega$ relative to those for the symmetric case. We also find a re-entrant behavior, where the number of vortex cores can decrease for large $\Omega$. In addition, stabilizing a vortex in a rotating asymmetric trap requires a minimum interaction strength. For a given asymmetry, the evolution of the variational parameters with increasing $\Omega$ shows two different types of transitions (sharp or continuous), depending on the strength of the interaction. We also investigate transitions to states with higher vorticity; the corresponding angular momentum increases continuously as a function of $\Omega$

NPN in the Dairy Ration

This archival publication may not reflect current scientific knowledge or recommendations. Current information available from the University of Minnesota Extension: https://www.extension.umn.edu

Feeding corn silage to dairy cattle

1 online resource (PDF, 8 pages)This archival publication may not reflect current scientific knowledge or recommendations. Current information available from the University of Minnesota Extension: https://www.extension.umn.edu

Stability of a vortex in a small trapped Bose-Einstein condensate

A second-order expansion of the Gross-Pitaevskii equation in the interaction parameter determines the thermodynamic critical angular velocity Omega_c for the creation of a vortex in a small axisymmetric condensate. Similarly, a second-order expansion of the Bogoliubov equations determines the (negative) frequency omega_a of the anomalous mode. Although Omega_c = -omega_a through first order, the second-order contributions ensure that the absolute value |omega_a| is always smaller than the critical angular velocity Omega_c. With increasing external rotation Omega, the dynamical instability of the condensate with a vortex disappears at Omega*=|omega_a|, whereas the vortex state becomes energetically stable at the larger value Omega_c. Both second-order contributions depend explicitly on the axial anisotropy of the trap. The appearance of a local minimum of the free energy for a vortex at the center determines the metastable angular velocity Omega_m. A variational calculation yields Omega_m=|\omega_a| to first order (hence Omega_m also coincides with the critical angular velocity Omega_c to this order). Qualitatively, the scenario for the onset of stability in the weak-coupling limit is the same as that found in the strong-coupling (Thomas-Fermi) limit.Comment: 8 pages, RevTe