Observation of modified hadronization in relativistic Au+Au collisions: a promising signature for deconfined quark-gluon matter

Measurements of identified particles from Au+Au collisions at $\sqrt{s_{_{NN}}}=200$ GeV are reviewed. Emphasis is placed on nuclear modification, baryon-to-meson ratios, and elliptic flow at intermediate transverse momentum ($1.5 < p_T < 5$ GeV/c). Possible connections between (1) these measurements, (2) the running coupling for static quark anti-quark pairs at finite temperature, and (3) the creation of a deconfined quark-gluon phase are presented. Modifications to hadronization in Au+Au collisions are proposed as a likely signature for the creation of deconfined colored matter.Comment: 8 pages, 5 figures, invited talk at the Strange Quark Matter 2004 conference, Cape Town, South Afric

Entanglement in a two-identical-particle system

The definition of entanglement in identical-particle system is introduced. The separability criterion in two-identical particle system is given. The physical meaning of the definition is analysed. Applications to two-boson and two-fermion systems are made. It is found new entanglement and correlation phenomena in identical-boson systems exist, and they may have applications in the field of quantum information.Comment: 4 page

Information transfer through a one-atom micromaser

We consider a realistic model for the one-atom micromaser consisting of a cavity maintained in a steady state by the streaming of two-level Rydberg atoms passing one at a time through it. We show that it is possible to monitor the robust entanglement generated between two successive experimental atoms passing through the cavity by the control decoherence parameters. We calculate the entanglement of formation of the joint two-atom state as a function of the micromaser pump parameter. We find that this is in direct correspondence with the difference of the Shannon entropy of the cavity photons before and after the passage of the atoms for a reasonable range of dissipation parameters. It is thus possible to demonstrate information transfer between the cavity and the atoms through this set-up.Comment: Revtex, 5 pages, 2 encapsulated ps figures; added discussion on information transfer in relation with cavity photon statistics; typos corrected; Accepted for Publicaiton in Europhysics Letter

Futures Trading in Plywood.

4 p

Marketing Texas Green-wrap Tomatoes.

16 p

Methods of Determining the Optimum Stage of Maturity for Picking Green-Wrap Tomatoes.

12 p

Entrance and survival of <i>Brucella pinnipedialis</i> hooded seal strain in human macrophages and epithelial cells

Marine mammal Brucella spp. have been isolated from pinnipeds (B. pinnipedialis) and cetaceans (B. ceti) from around the world. Although the zoonotic potential of marine mammal brucellae is largely unknown, reports of human disease exist. There are few studies of the mechanisms of bacterial intracellular invasion and multiplication involving the marine mammal Brucella spp. We examined the infective capacity of two genetically different B. pinnipedialis strains (reference strain; NTCT 12890 and a hooded seal isolate; B17) by measuring the ability of the bacteria to enter and replicate in cultured phagocytes and epithelial cells. Human macrophage-like cells (THP-1), two murine macrophage cell lines (RAW264.7 and J774A.1), and a human malignant epithelial cell line (HeLa S3) were challenged with bacteria in a gentamicin protection assay. Our results show that B. pinnipedialis is internalized, but is then gradually eliminated during the next 72 – 96 hours. Confocal microscopy revealed that intracellular B. pinnipedialis hooded seal strain colocalized with lysosomal compartments at 1.5 and 24 hours after infection. Intracellular presence of B. pinnipedialis hooded seal strain was verified by transmission electron microscopy. By using a cholesterol-scavenging lipid inhibitor, entrance of B. pinnipedialis hooded seal strain in human macrophages was significantly reduced by 65.8 % (± 17.3), suggesting involvement of lipid-rafts in intracellular entry. Murine macrophages invaded by B. pinnipedialis do not release nitric oxide (NO) and intracellular bacterial presence does not induce cell death. In summary, B. pinnipedialis hooded seal strain can enter human and murine macrophages, as well as human epithelial cells. Intracellular entry of B. pinnipedialis hooded seal strain involves, but seems not to be limited to, lipid-rafts in human macrophages. Brucella pinnipedialis does not multiply or survive for prolonged periods intracellulary