Bees use floral colour as a major long distance orientation cue. While it is known for bumblebees and honeybees that dominant wavelength (≙ colour hue), colour contrast and spectral purity (≙ saturation) are crucial for flower detection and discrimination, only little is known about colour preferences in stingless bees (Meliponini). In this experiment freely flying workers of two Brazilian species of stingless bees–Partamona helleri and Melipona bicolor–were tested for colour preferences concerning the colour parameters dominant wavelength, spectral purity and intensity (≙ brightness). Each individual bee had to perform 57 tests, in which a definite series of dual choices between colour stimuli varying in intensity, spectral purity or domin...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
The colour discrimination of individual free-flying honeybees (Apis mellifera) was tested with simul...
This is the final version. Available on open access from te Royal Society via the DOI in this record...
Bees use floral colour as a major long distance orientation cue. While it is known for bumblebees an...
Innate preferences promote the capacity of pollinators to find flowers. Honeybees and bumblebees hav...
Honey bees (Apis mellifera Linnaeus, 1758) potentially rely on a variety of visual cues when searchi...
Bee pollinators interact with flowers in a complex signal-receiver system. Chromatic traits that all...
Colour vision was first demonstrated with behavioural experiments in honeybees 100 years ago. Since ...
Adrian Horridge Biological Sciences, Australian National University, Canberra, ACT, Australia Abstr...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Free-flying bumblebees (Bombus terrestris Linnaeus 1758) were trained to visit homogeneously coloure...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Bumblebee (Bombus terrestris) discrimination of targets with broadband reflectance spectra was teste...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
The colour discrimination of individual free-flying honeybees (Apis mellifera) was tested with simul...
This is the final version. Available on open access from te Royal Society via the DOI in this record...
Bees use floral colour as a major long distance orientation cue. While it is known for bumblebees an...
Innate preferences promote the capacity of pollinators to find flowers. Honeybees and bumblebees hav...
Honey bees (Apis mellifera Linnaeus, 1758) potentially rely on a variety of visual cues when searchi...
Bee pollinators interact with flowers in a complex signal-receiver system. Chromatic traits that all...
Colour vision was first demonstrated with behavioural experiments in honeybees 100 years ago. Since ...
Adrian Horridge Biological Sciences, Australian National University, Canberra, ACT, Australia Abstr...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Free-flying bumblebees (Bombus terrestris Linnaeus 1758) were trained to visit homogeneously coloure...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
Bumblebee (Bombus terrestris) discrimination of targets with broadband reflectance spectra was teste...
Color discrimination thresholds proposed by receptor-noise type models are frequently used in animal...
The colour discrimination of individual free-flying honeybees (Apis mellifera) was tested with simul...
This is the final version. Available on open access from te Royal Society via the DOI in this record...