As noted in Chaps. 1 and 9, zirconium alloy components can fail by a time-dependent mechanism of cracking if hydrides can preferentially form and subsequently crack at locations of elevated tensile stress. This process of time-dependent hydride cracking, called delayed hydride cracking (DHC), is based on the mechanism of diffusion of hydrogen to a region of elevated tensile stress followed by nucleation, growth, and fracture of the hydrided region. By repeating these steps, a crack can propagate in a component at a rate that, above a threshold stress intensity factor, K IH ; is mainly dependent on temperature. In this chapter we present the status of the present state of understanding of DHC in zirconium alloys, emphasizing the connections between the models developed and the experimental data. The intent of this chapter is not to provide an exhaustive review of the literature but to focus on results that are deemed to have collectively advanced our understanding of this phenomenon. This chapter is divided into two main parts, the first part dealing with DHC propagation, the other with DHC initiation. Although it may appear backwards to start with DHC propagation rather than initiation, this approach is consistent with the historical development of the field and thus also helps somewhat in simplifying the exposition. Readers wishing to obtain a succinct recent overview of DHC and other aspects of the effects of hydrogen and hydrides on the integrity of zirconium alloys are referred to a recent review by Coleman [15]. In addition, an earlier review by Northwood and Kosasih [47] provides a comprehensive summary account of work published in this field up to the date of that publication.M. P. Puls, The Effect of Hydrogen and Hydrides on the Integrity of Zirconium Alloy Components, Engineering Materials,