Trends in Neurosciences
Research FocusFrom synchrony to sparseness
Section snippets
Neural circuits and neural code in the locust olfactory system
The olfactory system of the locust has been a remarkable model system for the study of the neural code (Fig. 1). Odorants are first detected by 90 000 olfactory receptors distributed on each antenna of the animal. Odorant identity is encoded in the olfactory receptor neurons by their mean firing rates, with many neurons responding to any particular odor. This spatially distributed code is then transformed into the spatial–temporal code found in the antennal lobe. The 830 projection neurons of
Intermediate conclusion
Perez-Orive et al. have shown that the properties of the Kenyon cells and the circuitry between the antennal lobe and the mushroom bodies favor the detection of the synchronized spatial–temporal patterns that are generated in the antennal lobe, and that this tuning results in a drastic transformation of the code for odor identity. It would be difficult, therefore, to argue that the synchrony found in the antennal lobe and all of the specialized circuitry apparently designed to detect it is an
Sparse codes
Theoreticians have provided answers to the first question ever since the term sparse-coding was proposed to describe neural code. In one of the earlier formulations, David Field suggested that sparse codes are ultimately related to the statistics of natural stimulus ensembles [17]. It is presently believed that many of the relevant features within natural scenes produce high-order correlations between the points within an image (e.g. curved edges within an image influence three-point
Dense spatial–temporal codes
The second theoretical question is whether the dense spatial–temporal code that was found at the level of the antennal lobe in the locust is a necessary intermediate step to ultimately obtaining the sparse representation found in the mushroom bodies. The answer to that question remains more elusive. One could envisage circuitry that generates a sparse code directly from a spatially distributed representation of sensory information, in which the information is represented by mean rates. For
Conclusion
The dense spatial–temporal neural code found in the AL is a highly efficient combinatorial code that might be needed both for the encoding of a large ensemble of odors with a limited number of neurons and for the formation of short-term olfactory memories. The sparse code found in the MB represents odor identity in a synthetic fashion that could facilitate the formation of long-term associative memories. The circuitry in the olfactory system of the locust exploits the synchronicity found in the
Acknowledgements
I would like to thank W. Vinje, J. Gallant and S. Shaevitz for their helpful comments on the manuscript.
References (26)
- et al.
Reliability and information transmission in spiking neurons
Trends Neurosci.
(1992) Is there a neural code?
Neurosci. Biobehav. Rev.
(1998)Spike timing in the mammalian visual system
Curr. Opin. Neurobiol.
(1999)- et al.
Spatio-temporal dynamics of odor representations in the mammalian olfactory bulb
Neuron
(2002) Unsupervised learning of granule cell sparse codes enhances cerebellar adaptive control
Neuroscience
(2001)Behavioral functions of the insect mushroom bodies
Curr. Opin. Neurobiol.
(2000)- et al.
Temporal encoding in nervous systems: a rigorous definition
J. Comput. Neurosci.
(1995) A systems perspective on early olfactory coding
Science
(1999)Information processing with population codes
Nat. Rev. Neurosci.
(2000)Temporal coding in the visual cortex: new vistas on integration in the nervous system
Trends Neurosci.
(1992)
Odour encoding by temporal sequences of firing in oscillating neural assemblies
Nature
Temporal representations of odors in an olfactory network
J. Neurosci.
Dynamic predictions: oscillations and synchrony in top-down processing
Nat. Rev. Neurosci.
Cited by (30)
Cortical Mechanisms of Smooth Eye Movements Revealed by Dynamic Covariations of Neural and Behavioral Responses
2008, NeuronCitation Excerpt :The more diverse pattern of responses of FEFSEM neurons may be critical for highly specific control of movement on the basis of cortical plans. Recent work in motor control in songbirds and representation of visual stimuli provides evidence that ethologically relevant stimuli and behaviors can be quite sparsely represented, with remarkable sensitivity and precision; here, we provide complementary evidence for temporally sparse coding in a similarly relevant behavioral space (Hahnloser et al., 2002; Theunissen, 2003; Vinje and Gallant, 2000). Because smooth pursuit is considerably slower than most behaviors, temporal sparseness in pursuit-related populations of neurons ought be more restricted than in songbird motor nuclei, which drive a less temporally correlated set of behaviors.
Sparse coding in the neocortex
2007, Evolution of Nervous SystemsSparse coding of sensory inputs
2004, Current Opinion in NeurobiologyNeural correlates of learned song in the avian forebrain: Simultaneous representation of self and others
2004, Current Opinion in NeurobiologyOn the sparse structure of natural sounds and natural images: Similarities, differences, and implications for neural coding
2019, Frontiers in Computational Neuroscience