Metastability and Coherence of Repulsive Polarons in a Strongly Interacting Fermi Mixture

Ultracold Fermi gases with tuneable interactions represent a unique test bed to explore the many-body physics of strongly interacting quantum systems. In the past decade, experiments have investigated a wealth of intriguing phenomena, and precise measurements of ground-state properties have provided exquisite benchmarks for the development of elaborate theoretical descriptions. Metastable states in Fermi gases with strong repulsive interactions represent an exciting new frontier in the field. The realization of such systems constitutes a major challenge since a strong repulsive interaction in an atomic quantum gas implies the existence of a weakly bound molecular state, which makes the system intrinsically unstable against decay. Here, we exploit radio-frequency spectroscopy to measure the complete excitation spectrum of fermionic 40K impurities resonantly interacting with a Fermi sea of 6Li atoms. In particular, we show that a well-defined quasiparticle exists for strongly repulsive interactions. For this "repulsive polaron" we measure its energy and its lifetime against decay. We also probe its coherence properties by measuring the quasiparticle residue. The results are well described by a theoretical approach that takes into account the finite effective range of the interaction in our system. We find that a non-zero range of the order of the interparticle spacing results in a substantial lifetime increase. This major benefit for the stability of the repulsive branch opens up new perspectives for investigating novel phenomena in metastable, repulsively interacting fermion systems.Comment: 11 pages, 9 figure

Redox Mechanisms Influencing cGMP Signaling in Pulmonary Vascular Physiology and Pathophysiology

The soluble form of guanylate cyclase (sGC) and cGMP signaling are major regulators of pulmonary vasodilation and vascular remodeling that protect the pulmonary circulation from hypertension development. Nitric oxide, reactive oxygen species, thiol and heme redox, and heme biosynthesis control mechanisms regulating the production of cGMP by sGC. In addition, a cGMP-independent mechanism regulates protein kinase G through thiol oxidation in manner controlled by peroxide metabolism and NADPH redox. Multiple aspects of these regulatory processes contribute to physiological and pathophysiological regulation of the pulmonary circulation, and create potentially novel therapeutic targets for the treatment of pulmonary vascular disease