Structural relaxations in humid silk fibers exposed to tensile stress have been reported to take place on a very wide range of time scales from a few milliseconds to several hours. The timedependence of the measured tensile force following a quasi-instantaneously applied external strain on the fibers can be understood in terms of a fractional viscoelastic relaxation function introducing memory effects by which the mechanical state of a fiber depends on its tensile history. An analog fractional relaxation also gives rise to the subdiffusion observed on picosecond time scales which governs the mobility of the amorphous polymer chains and adsorbed water on the molecular level. The reduction of the subdiffusive memory effect in stretched fibers compared to native fibers is consistent with the higher order of the polymers in the stretched state.