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Sub-Poisson Light

Jan Peřina

Published Jan 1, 1986• 0 citations
OpenAlex

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Yksittäisfotonilähteen käyttö yksittäisfotonivasteiden mittaamiseen verkkokalvon sauvasoluissa

Jussi Tiihonen

Our eyes are able to encode information from broad daylight down to only a handful of photons, but could we perceive a single photon? For decades the intrinsic Poisson variation of classical light sources has prevented definitive answers to this question. However, recent advances in quantum optics and non-classical light sources have reignited new interest in the question. Studies relying on sub-Poisson light sources have postulated that it is possible to produce sub-Poisson biological response distributions along the visual pathway, and even claimed that humans can perceive single photons. However, unambiguous experimental evidence for the prerequisite of sub-Poisson response statistics in the visual sciences has not been provided, that is, to which extent biological response statistics can differ between Poisson and sub-Poisson stimulation when taking retinal single-photon signal losses into account. In this thesis, we use a state-of-the-art sub-Poisson light source combined with the suction pipette technique to stimulate retinal rods in an axial geometry and measure their single-photon signal losses. We resolve the constraints set by the loss of single-photon signals to biological signal statistics from rods to human psychophysics. We show that due to the loss of single-photon signals it is impossible to distinguish the response distributions originating from Poisson or sub-Poisson light sources in the retina and at the level of perception on a biologically relevant timescale. Our results require fundamental re-evaluation of the previous results relying on sub-Poisson light stimulation in vision.

•Dec 16, 2019•0 citations
We report the generation of ultraviolet (253.7-nm) sub-Poisson light from Hg vapor excited by inelastic collisions with a space-charge-limited (quiet) electron beam. This first stationary sub-Poisson light source is only weakly so, with a Fano factor that is between two and three standard deviations below that for Poisson light. This is principally because of optical losses in the experimental apparatus. There does not appear to be any fundamental limit that impedes the techniques from being used to produce an intense cw light source that is also arbitrarily sub-Poisson.
Our eyes are able to encode information from broad daylight down to only a handful of photons, but could we perceive a single photon? For decades the intrinsic Poisson variation of classical light sources has prevented definitive answers to this question. However, recent advances in quantum optics and non-classical light sources have reignited new interest in the question. Studies relying on sub-Poisson light sources have postulated that it is possible to produce sub-Poisson biological response distributions along the visual pathway, and even claimed that humans can perceive single photons. However, unambiguous experimental evidence for the prerequisite of sub-Poisson response statistics in the visual sciences has not been provided, that is, to which extent biological response statistics can differ between Poisson and sub-Poisson stimulation when taking retinal single-photon signal losses into account. In this thesis, we use a state-of-the-art sub-Poisson light source combined with the suction pipette technique to stimulate retinal rods in an axial geometry and measure their single-photon signal losses. We resolve the constraints set by the loss of single-photon signals to biological signal statistics from rods to human psychophysics. We show that due to the loss of single-photon signals it is impossible to distinguish the response distributions originating from Poisson or sub-Poisson light sources in the retina and at the level of perception on a biologically relevant timescale. Our results require fundamental re-evaluation of the previous results relying on sub-Poisson light stimulation in vision.