An experimental and morphological analysis of the tail bud mesenchyme of the chick embryo.

In the chick embryo, the tail bud reaches its maximum length at about stage 22 of Hamburger and Hamilton, after which it starts to regress. By this stage the neural tube and notochord extend right to the tip of the tail, but the somites do not do so, the terminal tail bud mesoderm never becoming segmented. The investigation is concerned with analysing why this mesoderm fails to segment. When tail buds were explanted to the chorio-allantoic membrane, they continued to form somites only until the "correct" number had segmented, i.e., the tail bud formed no more somites when isolated from the embryo than it would have formed if undisturbed. Morphological studies suggest that in the normal embryo massive cell death overtakes the tail bud mesoderm before it can segment. It is suggested therefore that cell death may be a contributory factor in preventing segmentation.

Establishment of the Neural Differentiation Pattern in the Prospective Prosencephalic Ectoderm of the Chick Embryo (Gallus domesticus): (neural induction/neural differentiation/prosencephalic differentiation/eye potency field).

Small graft pieces (size: 0.15 × 0.2 mm to 0.1 × 0.4 mm and 0.25 × 0.25 mm) were isolated from the prospective prosencephalic ectoderm of the definitive primitive streak (st. 4) and head process (st. 5) chick blastoderms, and cultured in vivo intracoelomically. In all 1437 graft pieces isolated from 448 donor blastoderms were transplanted into the coelom of 941 host embryos; 216 hosts died before reaching 12 days. The 725 surviving hosts, which carried 1241 implants, yielded 304 analysable grafts. The very small size of the isolates affected the recovery rate. The histological analysis of the recovered grafts reveals that the frequency of neuralization was higher in the grafts isolated from the central region of the prospective prosencephalic ectoderm than in those from its peripheral region. A centrifugal extension of differentiation tendencies of prosencephalic structures was observed from st. 4 to st. 5. At st. 5 frequency of telencephalic structures was high in the grafts of the anterior region, whereas that of diencephalic structures was high in those of the more posterior region. Eye structures (retina as well as tapetum) differentiated in an area measuring ca. 0.4 × 0.1 mm extending transversely about 0.1 mm anterior to the head process at st. 5. Structural elements of the lens were not observed in any graft.