Of all extant invertebrate animals the Enteropneusts come nearest to the Chordonia in virtue of these peculiar characters; hence we may regard them as the survivors of the ancient gut-breathing Vermalia from which the Chordonia also have descended. Again, of all the chorda-animals the Copelata (Figure 2.225) and the tailed larvae of the ascidia approach nearest to the young Balanoglossus. Both are, on the other hand, very closely related to the Amphioxus, the Primitive Vertebrate of which we have considered the importance (Chapters 2.16 and 2.17). As we saw there, the unarticulated Tunicates and the articulated Vertebrates must be regarded as two independent stems, that have developed in divergent directions. But the common root of the two stems, the extinct group of the Prochordonia, must be sought in the vermalia stem; and of all the living Vermalia those we have considered give us the safest clue to their origin. It is true that the actual representatives of the important groups of the Copelata, Balanoglossi, Nemertina, Icthydina, etc., have more or less departed from the primitive model owing to adaptation to special environment. But we may just as confidently affirm that the main features of their organisation have been preserved by heredity.
We must grant, however, that in the whole stem-history of the Vertebrates the long stretch from the Gastraeads and Platodes up to the oldest Chordonia remains by far the most obscure section. We might frame another hypothesis to raise the difficulty—namely, that there was a long series of very different and totally extinct forms between the Gastraea and the Chordaea. Even in this modified chordaea-theory the six fundamental organs of the chordula would retain their great value. The medullary tube would be originally a chemical sensory organ, a dorsal olfactory tube, taking in respiratory-water and food by the neuroporus in front and conveying them by the neurenteric canal into the primitive gut. This olfactory tube would afterwards become the nervous centre, while the expanding gonads (lying to right and left of the primitive mouth) would form the coeloma. The chorda may have been originally a digestive glandular groove in the dorsal middle line of the primitive gut. The two secondary gut-openings, mouth and anus, may have arisen in various ways by change of functions. In any case, we should ascribe the same high value to the chordula as we did before to the gastrula.
In order to explain more fully the chief stages in the advance of our race, I add the hypothetical sketch of man's ancestry that I published in my Last Link 1 to 2. Protophytes. : 1. Monera. Without nucleus. : Chromacea. (Chroococcus.) Phycochromacea. 1 to 2. Protophytes. : 2. Algaria. Unicellular algae. : 2. Paulotomea. Palmellacea. Eremosphaera. 3 to 5. Protozoa. : 3. Lobosa. Unicellular (amoebina) rhizopods. : 3. Amoebina. Amoeba Leucocyta. 3 to 5. Protozoa. : 4. Infusoria. Unicellular. : 4. Flagellata. Euflagellata. Zoomonades.A. MAN'S GENEALOGICAL TREE, FIRST HALF: EARLIER SERIES OF ANCESTORS, WITHOUT FOSSIL EVIDENCE.
COLUMN 1 : CHIEF STAGES. COLUMN 2 : ANCESTRAL STEM-GROUPS. COLUMN 3 : LIVING RELATIVES OF ANCESTORS.
STAGES 1 TO 5. PROTIST ANCESTORS. UNICELLULAR ORGANISMS.