Epstein Secrets

ns of probability), we notice that /og70(0.5) = 0.693147 and /og70(0.25) = 1.386294 and that 0.693147 + 0.693147 = 1.386294. The dot-dash choices of Morse code machines, the go, no-go gates of transistors, the open versus closed ion channel-mediated neuronal membrane discharge and the left, right spins

occupancy of these possibles, the probables, form the bases for the computation of these two kinds of entropies. For example, the work of Paulus and Geyer showed that the administration of a very small amount of stimulant drug, compared with a salt water control, led to an increase in the first measure

mical system, such as nerve membrane equations as above, or in the aggregate, the middle layer of a completely connected neural network, can encode, Morse code-like, messages (Paulus et al, 1989). Bifurcations in Biologically Relevant Dynamical Systems Bifurcations, “splitting into (two) branches,” ar

cal aphorism that captures the fresh spiritual state of each moment’s openness and readiness, the in- between entropies for new information surprise. Geyer and Martin Paulus found that entheogenic agents such as Ecstasy also increased the complexity of the patterns of spontaneous motor movement made by r

ence not distance preserving ) representation of a difficult to characterize system of “geodesics on surfaces of negative curvature” (Hadamard, 1898; Morse, 1917; Morse and Hedlund, 1938). Geodesics here are the shortest lines in this curved, non-Euclidean space in which nearby lines spread apart and far

temporal and spatial patterns of rat exploratory behavior have been used to discriminate among stimulant drug effects (Paulus et al, 1990; Paulus and Geyer, 1992). Similar computations involving the symbolic dynamics and disallowed transitions have been used to study the complexity of the the EEG (Xu, 19