Search results
Results from the WOW.Com Content Network
In frog embryos, gastrulation initiates at the site identified as the gray crescent, located on the future dorsal side of the embryo, slightly below the equatorial region. This process involves cells migrating inward to form a structure similar to a blastopore .
During gastrulation cells migrate to the interior of the blastula, subsequently forming two (in diploblastic animals) or three (triploblastic) germ layers. The embryo during this process is called a gastrula. The germ layers are referred to as the ectoderm, mesoderm and endoderm.
Before gastrulation, the embryo is a continuous epithelial sheet of cells; by the end of gastrulation, the embryo has begun differentiation to establish distinct cell lineages, set up the basic axes of the body (e.g. dorsal–ventral, anterior–posterior), and internalized one or more cell types including the prospective gut. [2]
Embryo: 1 to 20 (about) Intracapsular. Development through cleavage, gastrulation, and appearance of neural tube and eventually gills and tail. Hatchling: 21 (about) to 24: Transition from relatively immobile embryo to an active, feeding tadpole. Specimens at these stages may sometimes be referred to as "larvae". Tadpole: 25 to 41
The primitive node (or primitive knot) is the organizer for gastrulation in most amniote embryos. In birds, it is known as Hensen's node, and in amphibians, it is known as the Spemann-Mangold organizer. It is induced by the Nieuwkoop center in amphibians, or by the posterior marginal zone in amniotes including birds.
Frog (Xenopus), as well as other amphibian, gastrulation serves as an excellent example of the role of convergent extension in embryogenesis. During gastrulation in frogs, the driving force of convergent extension is the morphogenic activity of the presumptive dorsal mesodermal cells; this activity is driven by the mesenchymal cells that lie ...
The filopodia—thin fibers formed by the mesenchyme cells, found in late gastrulation—contract to drag the tip of the archenteron across the blastocoel. The endoderm of the archenteron will fuse with the ectoderm of the blastocoel wall. At this point gastrulation is complete, and the embryo has a functional digestive tube.
In the frog Xenopus laevis, the animal pole is heavily pigmented while the vegetal pole remains unpigmented. [4] A pigment pattern provides the oocyte with features of a radially symmetrical body with a distinct polarity. The animal hemisphere is dark brown, and the vegetal hemisphere is only weakly pigmented.