Abstract
Action spectroscopy — the measurement, as a function of wavelength, of the sensitivity of a particular biological response or effect — is a standard approach towards identifying receptor pigment(s) for photobiological phenomena (Jagger, 1967; Shropshire, 1972; Hartmann, 1983; Schäfer et al., 1983; Schafer and Fukshansky, 1984; Galland, 1987). Comparison of an action spectrum with absorption spectra of known pigments often reveals the identity of the pigment, or class of pigments, involved. Some action spectra simply show the magnitude of a response as a function of wavelength, under conditions where a standard photon fluence (or fluence rate) is applied in all measurements. The difficulty with this expedient approach is that the response may well depend nonlinearly on the fluence. Such nonlinearity can introduce severe distortion into an action spectrum obtained in this way. The preferred method, instead, is to measure a separate fluence-response curve for each wavelength of interest, and then to determine the photon fluence needed to elicit a standard response level, for example 50% of maximum response. The reciprocal of the requisite photon fluence represents the sensitivity of the system, and is used as the ordinate of the action spectrum.
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References
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Lipson, E.D. (1991). Action Spectroscopy. In: Lenci, F., Ghetti, F., Colombetti, G., Häder, DP., Song, PS. (eds) Biophysics of Photoreceptors and Photomovements in Microorganisms. NATO ASI Series, vol 211. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5988-3_24
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DOI: https://doi.org/10.1007/978-1-4684-5988-3_24
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