Nuclear condensation during spermiogenesis in the ostrich follows the basic pattern established in other vertebrates. The fine granular nuclear substance of early spermatids is gradually replaced by numbers of coarse dense granules which appear to arise by aggregation of smaller dispersed elements of the chromatin. The granules increase in size and eventually coalesce to form the compact homogenous mass of chromatin typical of the mature sperm. In ostrich spermatids, however, the aggregation of the nuclear material produces large numbers of longitudinally oriented rod-shaped structures in addition to some granular material. Although fibrillar chromatin has been observed during spermiogenesis in a number of vertebrate species, the hollow nature of the rod-shaped chromatin granules in ostrich spermatids is a unique phenomenon. The spiralisation of the chromatin material observed in ostrich spermatids and in some other nonpasserine birds is possibly related to the reduction in nuclear length demonstrated during spermiogenesis in these species. In common with other nonpasserine birds, spermiogenesis in the ostrich is characterised by the appearance both of a circular and a longitudinal manchette. The circular manchette consists of a single row of microtubules reinforced by additional peripherally arranged microtubules. Links between adjacent microtubules, and between the nucleolemma and some of the microtubules, are evident. The longitudinal manchette consists of arrays of interconnected microtubules arranged in approximately 4–6 staggered, ill defined rows. This structure seems to originate as a result of the rearrangement of the microtubules of the circular manchette and is only formed once the process of chromatin condensation is well advanced. Based on the sequence of morphological events observed during spermiogenesis in the ostrich, it is concluded that the circular manchette is responsible for the initial transformation in shape of the spermatid nucleus. Thereafter, the chromatin condenses independently within the confines of the nucleolemma with the circular manchette merely acting to maintain the shape of the nucleus while this process is underway, to compress the nuclear membrane, and possibly to orientate the subunits of the condensing chromatin. The longitudinal manchette appears to assist in the translocation of material during spermatid elongation. There are indications that the developing acrosome is instrumental in effecting nuclear shaping of the apical (subacrosomal) head region of the ostrich spermatid.