On variability in the density of corticocortical and thalamocortical connections.

Variability is an important but neglected aspect of connectional neuroanatomy. The quantitative density of the 'same' corticocortical or thalamocortical connection may vary by over two orders of magnitude between different injections of the same tracer. At present, however, the frequency distribution of connection densities is unknown. Therefore, it is unclear what kind of sampling strategies or statistical methods are appropriate for quantitative studies of connectivity. Nor is it clear if the measured variability represents differences between subjects, or if it is simply a consequence of intra-individual differences resulting from experimental technique and the exact placement of tracers relative to local spatial and laminar variation in connectivity. We used quantitative measurements of the density of a large number of corticocortical and thalamocortical connections from our own laboratories and from the literature. Variability in the density of given corticocortical and thalamocortical connections is high, with the standard deviation of density proportional to the mean. The frequency distribution is close to exponential. Therefore, analysis methods relying on the normal distribution are not appropriate. We provide an appendix that gives simple statistical guidance for samples drawn from exponentially distributed data. For a given corticocortical or thalamocortical connection density, between-individual standard deviation is 0.85 to 1.25 times the within-individual standard deviation. Therefore, much of the variability reported in conventional neuroanatomical studies (with one tracer deposited per animal) is due to within-individual factors. We also find that strong, but not weak, corticocortical connections are substantially more variable than thalamocortical connections. We propose that the near exponential distribution of connection densities is a simple consequence of 'patchy' connectivity. We anticipate that connection data will be well described by the negative binomial, a class of distribution that applies to events occurring in clumped or patchy substrates. Local patchiness may be a feature of all corticocortical connections and could explain why strong corticocortical connections are more variable than strong thalamocortical connections. This idea is supported by the columnar patterns of many corticocortical but few thalamocortical connections in the literature.

[1]  J. Sjöstrand,et al.  Axonal uptake and retrograde transport of exogenous proteins in the hypoglossal nerve. , 1971, Brain research.

[2]  A. Rosenquist,et al.  Corticocortical connections among visual areas in the cat , 1984, The Journal of comparative neurology.

[3]  C. Cherniak The Bounded Brain: Toward Quantitative Neuroanatomy , 1990, Journal of Cognitive Neuroscience.

[4]  S Shipp,et al.  Visuotopic organization of the lateral suprasylvian area and of an adjacent area of the ectosylvian gyrus of cat cortex: A physioligical and connectional study , 1991, Visual Neuroscience.

[5]  A. Dobson,et al.  Patterns of macroparasite aggregation in wildlife host populations , 1998, Parasitology.

[6]  C. Blakemore,et al.  Analysis of connectivity in the cat cerebral cortex , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  V. Marchi,et al.  Sulla degenerazioni discendenti consecutive a lesioni sperimentali in diversa zone della corteccia cerebrale , 1888 .

[8]  E. DeYoe,et al.  Segregation of efferent connections and receptive field properties in visual area V2 of the macaque , 1985, Nature.

[9]  V. Montero Topography of the cortico-cortical connections from the striate cortex in the cat. , 1981, Brain, behavior and evolution.

[10]  B. Payne,et al.  Thalamic and cortical projections to middle suprasylvian cortex of cats: constancy and variation , 1997, Experimental Brain Research.

[11]  D. J. Felleman,et al.  Distributed hierarchical processing in the primate cerebral cortex. , 1991, Cerebral cortex.

[12]  J. E. Rose,et al.  Structure and relations of limbic cortex and anterior thalamic nuclei in rabbit and cat , 1948, The Journal of comparative neurology.

[13]  A. Rosenquist,et al.  Connections of the multiple visual cortical areas with the lateral posterior-pulvinar complex and adjacent thalamic nuclei in the cat , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  B. Payne,et al.  Survival and death of neurons in cortical area PMLS after removal of areas 17, 18, and 19 from cats and kittens. , 1991, Cerebral cortex.

[15]  C. Olson,et al.  Organization of cortical and subcortical projections to medial prefrontal cortex in the cat , 1988, The Journal of comparative neurology.

[16]  J. Scannell Determining cortical landscapes , 1997, Nature.

[17]  W. E. Clark THE VISUAL CENTRES OF THE BRAIN AND THEIR CONNEXIONS , 1942 .

[18]  D. Pandya,et al.  Architecture and Connections of Cortical Association Areas , 1985 .

[19]  C. Gerfen,et al.  An anterograde neuroanatomical tracing method that shows the detailed morphology of neurons, their axons and terminals: Immunohistochemical localization of an axonally transported plant lectin,Phaseolus vulgaris leucoagglutinin (PHA-L) , 1984, Brain Research.

[20]  H. Sherk Coincidence of patchy inputs from the lateral geniculate complex and area 17 to the cat's clare‐bishop area , 1986, The Journal of comparative neurology.

[21]  C R Olson,et al.  Organization of cortical and subcortical projections to anterior cingulate cortex in the cat , 1988, The Journal of comparative neurology.

[22]  S. Shipp,et al.  The functional logic of cortical connections , 1988, Nature.

[23]  W. E. Le Gros Clark,et al.  THE STRUCTURE AND CONNECTIONS OF THE THALAMUS , 1932 .

[24]  S. Poljak,et al.  An experimental study of the association callosal, and projection fibers of the cerebral cortex of the cat , 1927 .

[25]  A. Hendrickson,et al.  The autoradiographic demonstration of axonal connections in the central nervous system. , 1972, Brain research.

[26]  S. Zeki,et al.  Modular Connections between Areas V2 and V4 of Macaque Monkey Visual Cortex , 1989, The European journal of neuroscience.

[27]  W. Nauta,et al.  Silver impregnation of degenerating axons in the central nervous system: a modified technic. , 1954, Stain technology.

[28]  S Shipp,et al.  Organization of reciprocal connections between area 17 and the lateral suprasylvian area of cat visual cortex , 1991, Visual Neuroscience.

[29]  V. Montero Topography of the cortico-cortical connections from the striate cortex in the cat. , 1981, Brain, behavior and evolution.

[30]  G. Casella,et al.  Statistical Inference , 2003, Encyclopedia of Social Network Analysis and Mining.

[31]  M. Young The organization of neural systems in the primate cerebral cortex , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[32]  The Spatial Distribution of Cabbage Butterfly Eggs , 1983 .

[33]  K. Yau,et al.  Cyclic GMP-sensitive conductance in outer segment membrane of catfish cones , 1985, Nature.

[34]  C R Olson,et al.  Cortical areas in the medial frontal lobe of the cat delineated by quantitative analysis of thalamic afferents , 1991, The Journal of comparative neurology.

[35]  C R Olson,et al.  Topographic organization of cortical and subcortical projections to posterior cingulate cortex in the cat: Evidence for somatic, ocular, and complex subregions , 1992, The Journal of comparative neurology.

[36]  Q. Mckellar,et al.  The processes influencing the distribution of parasitic nematodes among naturally infected lambs , 1998, Parasitology.