Grouped convergence of noisy and stimulus-driven synaptic inputs is likely in all network configurations.
A. A simple, biologically-inspired model of Ca-Calmodulin reaction pathway.
B. The Ca-Calmodulin model shows selectivity for grouped inputs. Inputs arriving in a grouped manner (2μm spacing) lead to a higher concentration of Ca4_CaM as opposed to dispersed inputs (10μm spacing).
C. Different kinds of stimulus-driven groups. ‘Stimulus-driven groups’ receive M or more connections from neurons belonging to any of the ensembles. They could be of 3 kinds: 1) ‘fully-mixed groups’ that receive at least one connection from each ensemble; 2) ‘partially-mixed groups’ that contain multiple inputs from the same ensemble while missing inputs from others; ‘homogeneous groups’ that receive inputs from a single ensemble. D. Active and inactive groups, and noise groups. In an active group, all inputs constituting a group are received, whereas an inactive group may be missing one or more inputs in the duration of occurrence of a group, in spite of being connected with the ensembles. ‘Noise groups’ are formed of M or more background inputs; a group composed of M or more inputs of any kind, either from the ensembles or from noise or a combination of both is referred to as ‘any group’.
E. Neurons classified as per the types of groups they receive. Note that the schematic is a qualitative representation. The sizes of the circles do not correspond to the cardinality of the sets.
F. Probability of occurrence of connectivity based fully-mixed group due to local convergence of ensemble inputs. Group size is the number of different ensembles. It also corresponds to the number of different ensembles that send axons to a group of zone length ‘Z’. The ‘CICR’ configuration overlaps with the ‘chem’ configuration of the corresponding network in F, G, J and K as they share the same zone length.
G. Probability of occurrence of connectivity based stimulus-driven group, which receives connections from any of the ensembles. Group size in G refers to the number of connections arriving from any of the ensemble neurons within zone length ‘Z’.
H. Probability of occurrence of noise group due to local noisy activation of synapses. Here the group size refers to the number of synapses activated within the zone of length ‘Z’.
I. Probability of occurrence of a group due to the convergence of either stimulus-driven inputs or noisy inputs or a combination of both. Hippo-chem overlaps with cortex-CICR as they have same value for R*D.
J, K. Probability of occurrence of active fully-mixed and active stimulus-driven groups respectively, wherein all inputs constituting a group are active. Shaded regions in F, G, H, I, J, K represent lower and upper bounds on the analytical equations for probability based on non-overlapping and overlapping cases, i.e., and in the equations.
L. Frequency distribution of groups based on the number of unique ensembles they receive connections from, for stimulus-driven groups that receive four or more ensemble inputs. Here, the total number of active ensembles in the presynaptic population is four.
M. Ratio of the probability of occurrence of an active stimulus-driven group to the probability of occurrence of any group on a neuron. This gives an indirect measure of signal to noise in the population. The mismatch seen between the analytical and simulated traces in the case of cortex-CICR is due to low sampling at higher group-sizes.