Photonic quantum technology relies on efficient sources of coherent single photons, the ideal carriers of quantum information. Heralded single photons from parametric down-conversion can approximate on-demand single photons to a desired degree, with high spectral purities achieved through group-velocity matching and tailored crystal nonlinearities. Here we propose crystal nonlinearity engineering techniques with sub-coherence-length domains. We first introduce a combination of two existing methods: a deterministic approach with coherence-length domains and probabilistic domain-width annealing. We then show how the same deterministic domain-flip approach can be implemented with sub-coherence length domains. Both of these complementary techniques create highly pure photons, outperforming previous methods, in particular for short nonlinear crystals matched to femtosecond lasers.
We describe delivery of femtosecond solitons at 800nm wavelength over five meters of hollow-core photonic bandgap fiber. The output pulses had a length of less than 300fs and an output pulse energy of around 65nJ, and were almost bandwidth limited. Numerical modeling shows that the nonlinear phase shift is determined by both the nonlinearity of air and by the overlap of the guided mode with the glass.
We present the first implementation of mid-infrared dual-comb spectroscopy with an optical parametric oscillator. Methane absorption spectroscopy was demonstrated with a resolution of 0.2 cm(-1) (5 GHz) at an acquisition time of ~10.4 ms over a spectral coverage at 2900-3050 cm(-1). The average power from each individual mid-infrared comb line was ~1 μW, representing a power level much greater than typical difference-frequency-generation sources. Mid-infrared dual-comb spectroscopy opens up unique opportunities to perform broadband spectroscopic measurements with high resolution, high requisition rate, and high detection sensitivity.
Similar forms often evolve repeatedly in nature, raising longstanding questions about the underlying mechanisms. Here we use repeated evolution in sticklebacks to identify a large set of genomic loci that change recurrently during colonization of new freshwater habitats by marine fish. The same loci used repeatedly in extant populations also show rapid allele frequency changes when new freshwater populations are experimentally established from marine ancestors. Dramatic genotypic and phenotypic changes arise within 5-7 years, facilitated by standing genetic variation and linkage between adaptive regions. Both the speed and location of changes can be predicted using empirical observations of recurrence in natural populations or fundamental genomic features like allelic age, recombination rates, density of divergent loci, and overlap with mapped traits. A composite model trained on these stickleback features can also predict the location of key evolutionary loci in Darwin’s finches, suggesting similar features are important for evolution across diverse taxa.
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