Related Experiment Video
Updated: Jul 16, 2026

Simultaneous Long-term Recordings at Two Neuronal Processing Stages in Behaving Honeybees
Published on: July 21, 2014
Temporal competition between odorants: effect of different time intervals on the perception of monorhinic and
1Laboratoire de Physiologie Neurosensorielle, UA CNRS 180, Université Claude Bernard Lyon 1, Villeurbanne, France.
Abstract:
Backward masking and its possible connection with the perception of odour mixtures has been investigated. Temporal competition between odorants in a binary mixture was tested by artificially creating a delay between one odour (the target) and a second, stronger, odour (the mask) during a single natural sniff. To test the influence of central versus peripheral competition, the same mixture was presented either monorhinically or dichorhinically. The delay (100 to 400 ms) did not influence intensity perception, indicating that intensities are integrated during the sniff irrespective of the temporal arrangement. In contrast, the number of qualities perceived was influenced by the delay: delays of 200 to 400 ms gave significant increases in the frequency of detection of a mixture, whereas synchronous mixtures favoured the perception of a single odour. Masking was also significantly stronger in dichorhinic mixtures. These effects are discussed in terms of retroactive masking which seems to be enhanced by dichorhinic mixtures, suggesting that masking has an important central component.
Related Concept Videos
Olfaction
The olfactory receptors are embedded in the cilia of the...
Stereoisomerism
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...

