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A stimulated Stokes Raman scattering-based approach for continuous wave supercontinuum generation in optical fibers
We report on a new and simple approach for continuous wave supercontinuum generation in optical fibers. Our new approach uses the effect of stimulated Stokes Raman scattering in a low loss fiber ring laser. By continuously pumping this ring laser with up to 19 W optical power we excited up to six Stokes orders and covered a wavelength range of 500 nm. Due to the feedback mechanism of the ring layout additional nonlinear effects occurred next to the plain generation of individual Stokes peaks. Eventually, these effects broaden and merge the separated Stokes peaks and create a single, connected continuous supercontinuum. By using the effect of stimulated Stokes Raman scattering, we do not rely on anomalous dispersion and modulation instability as typically required for continuous wave supercontinuum generation. © 2019 Astro Ltd.
Intra-cavity measurement concept of dispersion properties with a tunable fiber-integrated laser
The dispersion properties of fibers depict a key characteristic to model the propagation of ultra-short pulses in waveguides. In the following, a new method is presented to directly measure the dispersion properties of fibers and optical components in the time domain. The analysis is based on pulse shape variations along the tuning range of a theta cavity fiber laser (TCFL) depending on the adjusted repetition rate. The automated measurement procedure, evaluating pulse symmetry, achieves a temporal sensitivity below 5 ps surpassing the resolution of the acquisition electronics. Exemplarily, two samples of Nufern PM980-XP fiber are investigated with an Yb-doped tunable TCFL retrieving the mean dispersion parameter D? by comparative measurements. The obtained results are compared to a reference method based on spectral interferometry. With deviations in D? between either approach of 0.3% and 1.3%, respectively, the results agree well within the measurement errors of the TCFL, verifying the presented concept. Due to the pulse formation process extending over multiple round trips, this approach achieves an enhanced sensitivity compared to competing direct temporal methods. Together with an alignment free operation, the fiber-integrated TCFL depicts a simple and robust concept showing potential in specific measurement scenarios such as in quality management. © 2019 Astro Ltd.
Influence of cell shape, inhomogeneities and diffusion barriers in cell polarization models
In silico experiments bear the potential for further understanding of biological transport processes by allowing a systematic modification of any spatial property and providing immediate simulation results. Cell polarization and spatial reorganization of membrane proteins are fundamental for cell division, chemotaxis and morphogenesis. We chose the yeast Saccharomyces cerevisiae as an exemplary model system which entails the shuttling of small Rho GTPases such as Cdc42 and Rho, between an active membrane-bound form and an inactive cytosolic form. We used partial differential equations to describe the membrane-cytosol shuttling of proteins. In this study, a consistent extension of a class of 1D reaction-diffusion systems into higher space dimensions is suggested. The membrane is modeled as a thin layer to allow for lateral diffusion and the cytosol is modeled as an enclosed volume. Two well-known polarization mechanisms were considered. One shows the classical Turing-instability patterns, the other exhibits wave-pinning dynamics. For both models, we investigated how cell shape and diffusion barriers like septin structures or bud scars influence the formation of signaling molecule clusters and subsequent polarization. An extensive set of in silico experiments with different modeling hypotheses illustrated the dependence of cell polarization models on local membrane curvature, cell size and inhomogeneities on the membrane and in the cytosol. In particular, the results of our computer simulations suggested that for both mechanisms, local diffusion barriers on the membrane facilitate Rho GTPase aggregation, while diffusion barriers in the cytosol and cell protrusions limit spontaneous molecule aggregations of active Rho GTPase locally.