Tunneling, dissipation, and superfluid transition in quantum Hall bilayers

We study bilayer quantum Hall systems at total Landau level filling factor $\nu=1$ in the presence of interlayer tunneling and coupling to a dissipative normal fluid. Describing the dynamics of the interlayer phase by an effective quantum dissipative XY model, we show that there exists a critical dissipation $\sigma_c$ set by the conductance of the normal fluid. For $\sigma > \sigma_c$, interlayer tunnel splitting drives the system to a $\nu=1$ quantum Hall state. For $\sigma <\sigma_c$, interlayer tunneling is irrelevant at low temperatures, the system exhibits a superfluid transition to a collective quantum Hall state supported by spontaneous interlayer phase coherence. The resulting phase structure and the behavior of the in-plane and tunneling currents are studied in connection to experiments.Comment: 4 RevTex pages, revised version, to appear in Phys. Rev. Let

Superconductivity-Related Insulating Behavior

We present the results of an experimental study of superconducting, disordered, thin-films of amorphous Indium Oxide. These films can be driven from the superconducting phase to a reentrant insulating state by the application of a perpendicular magnetic field ($B$). We find that the high-$B$ insulator exhibits activated transport with a characteristic temperature, $T_I$. $T_I$ has a maximum value ($T_{I}^p$) that is close to the superconducting transition temperature ($T_c$) at $B$ = 0, suggesting a possible relation between the conduction mechanisms in the superconducting and insulating phases. $T_{I}^p$ and $T_c$ display opposite dependences on the disorder strength.Comment: Tex file and 5 figures; Revised version; To appear in Phys. Rev. Lett. (2004

Transmission of viruses via our microbiomes.

BackgroundBacteria inhabiting the human body have important roles in a number of physiological processes and are known to be shared amongst genetically-related individuals. Far less is known about viruses inhabiting the human body, but their ecology suggests they may be shared between close contacts.ResultsHere, we report the ecology of viruses in the guts and mouths of a cohort and demonstrate that substantial numbers of gut and oral viruses were shared amongst genetically unrelated, cohabitating individuals. Most of these viruses were bacteriophages, and each individual had distinct oral and gut viral ecology from their housemates despite the fact that some of their bacteriophages were shared. The distribution of bacteriophages over time within households indicated that they were frequently transmitted between the microbiomes of household contacts.ConclusionsBecause bacteriophages may shape human oral and gut bacterial ecology, their transmission to household contacts suggests they could have substantial roles in shaping the microbiota within a household

Microbial diversity in individuals and their household contacts following typical antibiotic courses.

BackgroundAntibiotics are a mainstay of treatment for bacterial infections worldwide, yet the effects of typical antibiotic prescriptions on human indigenous microbiota have not been thoroughly evaluated. We examined the effects of the two most commonly prescribed antibiotics (amoxicillin and azithromycin) in the USA to discern whether short-term antibiotic courses may have prolonged effects on human microbiota.ResultsWe sampled the feces, saliva, and skin specimens from a cohort of unrelated, cohabitating individuals over 6 months. An individual in each household was given an antibiotic, and the other a placebo to discern antibiotic impacts on microbiota, as well as determine whether antibiotic use might reshape the microbiota of each household. We observed household-specific patterns of microbiota on each body surface, which persevered despite antibiotic perturbations. While the gut microbiota within an individual became more dissimilar over time, there was no evidence that the use of antibiotics accelerated this process when compared to household members. There was a significant change in microbiota diversity in the gut and mouth in response to antibiotics, but analogous patterns were not observed on the skin. Those who received 7 days of amoxicillin generally had greater reductions in diversity compared to those who received 3 days, in contrast to those who received azithromycin.ConclusionsAs few as 3 days of treatment with the most commonly prescribed antibiotics can result in sustained reductions in microbiota diversity, which could have implications for the maintenance of human health and resilience to disease