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Abstract Synchronized optical pulses are widely used. We report here characterization and measurement of synchronized femtosecond and picosecond pulses from a Ti:Sapphire laser (nominally 800 nm) and a Nd:YAG laser (1064 nm), respectively. Synchronization is achieved by utilizing soliton self-frequency shift in a photonic-crystal fiber that allows the 800 nm femtosecond oscillator to seed the third-harmonic generation (355 nm) of picosecond regenerative amplifier. The relative timing jitter between the amplified femtosecond and the third-harmonic generation of picosecond pulses is (710 ± 160) fs, which is only (1.17 ± 0.26)% of the picosecond pulse duration. This work paves way for applications in stimulated Raman scattering spectroscopy and amplification. 

Fungal melanins represent a resource for important breakthroughs in industry and medicine, but the characterization of their composition, synthesis, and structure is not well understood. Raman spectroscopy is a powerful tool for the elucidation of molecular composition and structure. In this work, we characterize the Raman spectra of wild-type Aspergillus fumigatus and Cryptococcus neoformans and their melanin biosynthetic mutants and provide a rough “map” of the DHN (A. fumigatus) and DOPA (C. neoformans) melanin biosynthetic pathways. We compare this map to the Raman spectral data of Aspergillus nidulans wild-type and melanin biosynthetic mutants obtained from a previous study. We find that the fully polymerized A. nidulans melanin cannot be classified according to the DOPA pathway; nor can it be solely classified according to the DHN pathway, consistent with mutational analysis and chemical inhibition studies. Our approach points the way forward for an increased understanding of, and methodology for, investigating fungal melanins.