Abstract

Recent interest in applying novel imaging techniques to infer optical resolution in compound eyes underscores the difficulty of obtaining direct measures of acuity. A widely used technique exploits the principal pseudopupil, a dark spot on the eye surface representing the ommatidial gaze direction and the number of detector units (ommatidia) viewing that gaze direction. However, dark-pigmented eyes, like those of honeybees, lack a visible pseudopupil. Attempts over almost a century to estimate optical acuity in this species are still debated. Here, we developed a method to visualize a stable, reliable pseudopupil by staining the photoreceptors with fluorescent dyes. We validated this method in several species and found it to outperform the dark pseudopupil for this purpose, even in pale eyes, allowing more precise location of the gaze centre. We then applied this method to estimate the sampling resolution in the frontal part of the eye of the honeybee forager. We found a broad frontal acute zone with interommatidial angles below 2° and a minimum interommatidial angle of 1.3°, a broader, sharper frontal acute zone than previously reported. Our study provides a new method to directly measure the sampling resolution in most compound eyes of living animals.

Highlights

  • Recent interest in applying novel imaging techniques to infer optical resolution in compound eyes underscores the difficulty of obtaining direct measures of acuity

  • For many years the ‘pseudopupil method’ has provided a more direct approach for measuring the axial directions of ommatidia in living insects. This method most often relies on the principal pseudopupil, a dark spot which results from light absorption by the pigment cells surrounding the crystalline cone and the photoreceptors close to the direction of g­ aze[22]

  • This dark pseudopupil shifts its position as the eye rotates, and changes shape according to the density of receptors sampling the local viewing direction

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Summary

Introduction

Recent interest in applying novel imaging techniques to infer optical resolution in compound eyes underscores the difficulty of obtaining direct measures of acuity. This induced fluorescent pseudopupil clearly moves across the eye surface (see Supplementary Information video 1, part 1), changing in its shape and dimensions in response to variations in the local photoreceptor (i.e. ommatidial) angular density, just as seen in the natural dark ­pseudopupil[22].

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