Abstract

Recent studies suggest that photophysiological parameters for intact substrates with depth (e.g., periphytic biofilms, microphytobenthos) are overestimated by pulse-amplitude modulated (PAM) fluorometry. This overestimation results from depth-integration effects, following the activation of deeper photosynthesizing layers by an attenuated light signal. To mitigate this error, we propose a novel slide-based thin-film technique in which fluorescence is measured on a vertically representative subsample of the biofilm, spread evenly on a microscope slide. We compared bias and precision for photosynthetic parameters estimated through conventional PAM fluorometry on intact biofilms and through our novel slide-based technique, both theoretically and empirically. Numerical simulations confirmed the consistent overestimation of key parameters for intact biofilms, with relative errors up to 145%, compared to, at most, 52% on thin films. Paired empirical observations likewise demonstrated that estimates based on intact biofilms were consistently higher (up to 248%, p < 0.001) than estimates from thin films. Numerical simulation suggested greater precision with the slide-based technique for homogeneous biofilms, but potentially less precision for heterogeneous biofilms with improper subsampling. Our empirical comparison, however, demonstrated some improvement in precision with the slide-based technique (e.g., the coefficient of variation for the maximum electron transport rate was reduced 30%, p = 0.009). We recommend the use of the slide-based technique, particularly for biofilms that are thick or have small light attenuation coefficients. Care should be taken, however, to obtain vertically representative subsamples of the biofilm for measurement.

Highlights

  • Pulse-amplitude modulated (PAM) fluorometry has emerged as a vital tool to assess physiological efficiencies of photosynthesizing organisms and communities

  • We use the depth-integration model presented in Serôdio [4] to test comparative predictions of bias and precision for both the new slide-based method and the traditional intact-biofilm method. We model both homogeneousphotic communities and heterogeneousphotic communities

  • We focused our t-test comparisons on standard deviation (SD) rather than coefficient of variation (CV), because we assumed that the slide and intact-biofilm methods were both estimating the same true parameter per sample; we used estimates of CV for more general comparisons of precision across parameters because of the wide variation in parameter magnitudes

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Summary

Introduction

Pulse-amplitude modulated (PAM) fluorometry has emerged as a vital tool to assess physiological efficiencies of photosynthesizing organisms and communities. The technique is both rapid and non-destructive and measures chlorophyll fluorescence in response to increasing levels of irradiance. These measurements yield relative electron transport rate (rETR) profiles over irradiance, or rapid light curves (RLCs), which are very similar in form to photosynthesis–irradiance (P–E) curves. Common photophysiological parameters estimated from the RLCs include the maximum electron transport rate (ETRm ), the minimum saturating irradiance (Ek ), and the photosynthetic efficiency (α) (e.g., [1,2,3]).

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