This preprint measured visual physiology in two sympatric Australian stingless bees using pattern electroretinograms (pERG) and eye casts. The larger Austroplebeia australis (ITW 1.27 mm) had ~5% more facets (3075.8 vs 2937.8) and larger facet diameters (13.2β22.51 Β΅m vs 11.04β19.69 Β΅m) than Tetragonula carbonaria (both p=0.04). Spatial resolving power was identical (0.53 cpd both species, p=0.96), while contrast sensitivity at 0.05 cpd was ~2.2Γ higher in A. australis (13.07 vs 5.99, p=0.009), with significance at nearly all spatial frequencies .
Strengths: Identical methods and stimulus protocol enable direct comparison with honeybee data (Ryan et al. 2020); mixed-effects modelling with Bonferroni correction is appropriate; body-size and facet-difference explanation is anatomically coherent (larger facets β more photons β higher contrast sensitivity, per Kirschfeld 1974) .
Limitations: Very small n (5 and 7 for morphology; n=5 each for pERG) from a single colony per species limits generalizability. Dark adaptation was capped at 10 minutes for animal welfare, which likely underestimates true sensitivity. Antennae were removed in T. carbonaria but kept in A. australis (necessary for survival), introducing an asymmetric handling effect. Facet diameter was measured only in the medio-frontal region, not whole-eye. The ecological interpretation (higher sensitivity enabling detection of specific petal shades) is speculative and explicitly acknowledged as untested .
Testing with full dark adaptation, larger multi-colony sampling, and behavioural confirmation (e.g., object avoidance or detection tasks) would either corroborate or challenge the physiological estimates. Internal anatomical data (rhabdom width, focal length) are missing and would be needed to confirm the mechanistic explanation for higher contrast sensitivity.
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