Write . The inverse coordinate formulas and are valid because . The multivariable chain rule gives
Applying these operators twice and using the symmetry of second derivatives,
Thus the wave equation is equivalent to
For each fixed , the partial derivative has zero derivative with respect to , so it is a function of alone. Taking an antiderivative in gives , where the integration constant may depend on . Hence
Conversely, direct partial differentiation verifies the wave equation for every twice differentiable pair . The two terms describe profiles moving left and right respectively at wave speed along the characteristic lines for the one-dimensional wave equation.
At , the initial conditions imply
Differentiate the first relation and solve for the two derivatives:
Fix a reference point and set . Taking antiderivatives gives
The constants must be opposite to preserve the first initial condition; the arbitrary constant of integration does not change . Substitution yields D'Alembert's formula:
The fundamental theorem of calculus verifies that its time derivative at zero is , and its value at zero is . The oriented integral also makes the formula valid for negative .
An antiderivative of the initial velocity is . Thus D'Alembert's formula gives
This is a positive Gaussian function moving right and a negative Gaussian function moving left. Their cancellation at gives the zero initial displacement, while direct differentiation gives .
For every , the profile is an odd function of , vanishes at , is positive for and negative for , and tends to zero at both spatial infinities. The signs follow from . The positive and negative lobes move farther apart as increases; for large separation they approach the individual unit-height Gaussian functions centred at . At finite separation the actual extrema lie slightly beyond these centres: writing , the positive global maximum occurs at the unique satisfying .
Figure 1.
Oppositely signed Gaussian wave profiles at two positive times
. Representative times with and show the odd function profile and increasing separation of its lobes. The individual component centres are , while their superposition slightly shifts the actual extrema. Details.

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