Thermonuclear X-ray Bursts: Theory vs. Observations

I review our theoretical understanding of thermonuclear flashes on accreting neutron stars, concentrating on comparisons to observations. Sequences of regular Type I X-ray bursts from GS 1826-24 and 4U 1820-30 are very well described by the theory. I discuss recent work which attempts to use the observed burst properties in these sources to constrain the composition of the accreted material. For GS 1826-24, variations in the burst energetics with accretion rate indicate that the accreted material has solar metallicity; for 4U 1820-30, future observations should constrain the hydrogen fraction, testing evolutionary models. I briefly discuss the global bursting behavior of burst sources, which continues to be a major puzzle. Finally, I turn to superbursts, which naturally fit into the picture as unstable carbon ignition in a thick layer of heavy elements. I present new time-dependent models of the cooling tails of superbursts, and discuss the various interactions between superbursts and normal Type I bursts, and what can be learned from them.Comment: 11 pages, 6 figures; to appear in Proc. of the 2nd BeppoSAX Meeting: "The Restless High-Energy Universe" (Amsterdam, May 5-8, 2003), E.P.J. van den Heuvel, J.J.M. in 't Zand, and R.A.M.J. Wijers (Eds

The rp Process Ashes from Stable Nuclear Burning on an Accreting Neutron Star

We calculate the nucleosynthesis during stable nuclear burning on an accreting neutron star. This is appropriate for weakly magnetic neutron stars accreting at near-Eddington rates in low mass X-ray binaries, and for most accreting X-ray pulsars. We show that the nuclear burning proceeds via the rapid proton capture process (rp process), and makes nuclei far beyond the iron group. The final mixture of nuclei consists of elements with a range of masses between approximately A=60 and A=100. The average nuclear mass of the ashes is set by the extent of helium burning via (alpha,p) reactions, and depends on the local accretion rate. Our results imply that the crust of these accreting neutron stars is made from a complex mixture of heavy nuclei, with important implications for its thermal, electrical and structural properties. A crustal lattice as impure as our results suggest will have a conductivity set mostly by impurity scattering, allowing more rapid Ohmic diffusion of magnetic fields than previously estimated.Comment: To appear in the Astrophysical Journal (33 pages, LaTeX, including 11 postscript figures

ActA Protozoologica Tolerance of Naked Amoebae to Low Oxygen Levels with an Emphasis on the Genus Acanthamoeba

Summary. Amoebae feed on attached bacteria within, and below, bacterial biofilms where they experience reduced oxygen levels. The implications of this were examined by comparing the migration (an index of growth) of thirteen strains of Acanthamoeba and five species of naked amoebae grown under microaerophilic and aerobic conditions. All amoebae replicated well under both conditions and twelve isolates migrated significantly faster under low oxygen. Only one isolate, Vannella sp., migrated further (presumably grew faster) under aerobic conditions. The data show most amoebae prefer low oxygen as befits the biofilm habitat. Interestingly, the eleven acanthamoeba strains that replicated faster under microaerophilic conditions were all T4 genotypes and included four strains isolated from patients with amoeba keratitis (AK) infections. This genotype is most frequently found in AK cases and it is suggested that strains of Acanthamoeba capable rapid growth in a biofilm of a poorly cleansed contact lens may be an important factor in the development of an effective infective dose when placed on the cornea

Tolerance of Naked Amoebae to Low Oxygen Levels with an Emphasis on the Genus Acanthamoeba

Amoebae feed on attached bacteria within, and below, bacterial biofilms where they experience reduced oxygen levels. The implications of this were examined by comparing the migration (an index of growth) of thirteen strains of Acanthamoeba and five species of naked amoebae grown under microaerophilic and aerobic conditions. All amoebae replicated well under both conditions and twelve isolates migrated significantly faster under low oxygen. Only one isolate, Vannella sp., migrated further (presumably grew faster) under aerobic conditions. The data show most amoebae prefer low oxygen as befits the biofilm habitat. Interestingly, the eleven acanthamoeba strains that replicated faster under microaerophilic conditions were all T4 genotypes and included four strains isolated from patients with amoeba keratitis (AK) infections. This genotype is most frequently found in AK cases and it is suggested that strains of Acanthamoeba capable of rapid growth in a biofilm of a poorly cleansed contact lens may enable amoebae to multiply and provide an infective dos e when placed onthe cornea

Antithymocyte Globulin Plus G-CSF Combination Therapy Leads to Sustained Immunomodulatory and Metabolic Effects in a Subset of Responders With Established Type 1 Diabetes.

Low-dose antithymocyte globulin (ATG) plus pegylated granulocyte colony-stimulating factor (G-CSF) preserves β-cell function for at least 12 months in type 1 diabetes. Herein, we describe metabolic and immunological parameters 24 months following treatment. Patients with established type 1 diabetes (duration 4-24 months) were randomized to ATG and pegylated G-CSF (ATG+G-CSF) (N = 17) or placebo (N = 8). Primary outcomes included C-peptide area under the curve (AUC) following a mixed-meal tolerance test (MMTT) and flow cytometry. "Responders" (12-month C-peptide ≥ baseline), "super responders" (24-month C-peptide ≥ baseline), and "nonresponders" (12-month C-peptide < baseline) were evaluated for biomarkers of outcome. At 24 months, MMTT-stimulated AUC C-peptide was not significantly different in ATG+G-CSF (0.49 nmol/L/min) versus placebo (0.29 nmol/L/min). Subjects treated with ATG+G-CSF demonstrated reduced CD4+ T cells and CD4+/CD8+ T-cell ratio and increased CD16+CD56hi natural killer cells (NK), CD4+ effector memory T cells (Tem), CD4+PD-1+ central memory T cells (Tcm), Tcm PD-1 expression, and neutrophils. FOXP3+Helios+ regulatory T cells (Treg) were elevated in ATG+G-CSF subjects at 6, 12, and 18 but not 24 months. Immunophenotyping identified differential HLA-DR expression on monocytes and NK and altered CXCR3 and PD-1 expression on T-cell subsets. As such, a group of metabolic and immunological responders was identified. A phase II study of ATG+G-CSF in patients with new-onset type 1 diabetes is ongoing and may support ATG+G-CSF as a prevention strategy in high-risk subjects