The visual ecology of avian photoreceptors.

By N. Hart. Progress in retinal and eye research, 2001

598 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Ecology, Evolution, Behavior and Systematics

View Paper: https://www.semanticscholar.org/paper/12f9b9889c148bd77bc832b83700b16e28aec4a9

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In Cellular and Molecular Neuroscience

In Ecology, Evolution, Behavior and Systematics

Citations in the corpus

Conspicuous males suffer higher predation risk: visual modelling and experimental evidence from lizards (2003, methodology): “However, birds are highly conserved in their visual pigment characteristics (reviewed in Hart 2001b), so the spectral sensitivities of”
Mimicry in coral reef fish: how accurate is this deception in terms of color and luminance? (2009, background): “However, the perception of color signals depends on the visual system of signal receivers, which often vary considerably between species (e.g., Lythgoe 1979; Jacobs 1993; Hart 2001; Losey et al. 2003).”
Camouflage through behavior in moths: the role of background matching and disruptive coloration (2015, unknown): “Hart NS. 2001.”
Plumage brightness predicts male mating success in the lekking golden-collared manakin, Manacus vitellinus (2006, background): “We calculated brightness or intensity of collar and beard by summing its reflectance from 300 to 700 nm, the approximate visible spectrum of most avian species (Hart, 2001).”
pavo: an R package for the analysis, visualization and organization of spectral data (2013, background): “2009), hormonal and genetic mechanisms regulating phenotype (Muller &Eens 2009), physiological processes involved in perceiving the signal (Hart 2001), and its adaptive and evolutionary patterns (Badyaev & Hill 2003; Darst et al.”
Egg coloration is correlated with female condition in eastern bluebirds (Sialia sialis) (2006, background): “Moreover, the UV-reflection peak of blue-green eggs may not have an important signaling function because avian vision is limited to wavelengths between 320 and 700 nm (Hart 2001).”
The role of chromatic and achromatic signals for fruit detection by birds (2006, methodology): “Physiological models of eye function (Vorobyev and Osorio 1998; Hart 2001; Vorobyev et al. 2001) increasingly allow such quantification (Heiling et al. 2003; e.g., Thery and Casas 2002).”
Experimental Evidence for Aposematism in the Dendrobatid Poison Frog Oophaga pumilio (2007, background): “Color vision is well known among birds, and it is likely that they are able to detect the conspicuous coloration of O. pumilio (as well as other dendrobatid frogs; Hart, 2001; Siddiqi et al., 2004).”
Influence of ambient light on the evolution of colour signals: comparative analysis of a Neotropical rainforest bird community (2004, background): “As birds have well-developed colour vision – sensitivity to UV, potential tetrachromacy (Chen & Goldsmith 1986; Hart 2001) – they offer a good example to question the role of ambient light on colour signals.”