In _Amphioxus_ and the Tunicata the early development of the central
nervous system is very much like that of the Vertebrata, but the later
stages are simpler, being without the cranial flexure. The Tunicata
are remarkable for the fact that the nervous system, though at first
hollow, becomes quite solid in the adult. In _Balanoglossus_ the
central nervous system is in part tubular, the canal being open at
each end. It arises, however, by delamination from the ectoderm, the
tube being a secondary acquisition. This is probably due to a
shortening of development, for the same feature is found in some
Vertebrata (Teleostei, _Lepidosteus_, &c.), where the central canal is
secondarily hollowed out in the solid keel-like mass which is
separated from the ectoderm. Parts of the central nervous system arise
by invagination in other groups; for instance, the cerebral ganglia of
_Dentalium_ are formed from the walls of two invaginations of
ectoderm, which eventually disappear at the anterior end of the body
(A. Kowalevsky, _Ann. Mus. Hist. Nat. Marseilles_, "Zoology," vol.
i.). In _Peripatus_ the cerebral ganglia arise in a similar way, but
in this case the cavities of the invagination become separated from
the skin and persist as two hollow appendages on the lower side of the
cerebral ganglia. In other Arthropods the cerebral ganglia arise in a
similar way, but the invaginations disappear in the adult. In
Nemertines the cerebral ganglia contain a cavity which communicates
with the exterior by a narrow canal. Finally, in certain Echinodermata
the ventral part of the central nervous system arises by the
invagination of a linear streak of ectoderm, the cavity of the
invagination persisting as the epineural canal.
Peripheral nervous system.
Although the central nervous system is almost always developed from the
ectoderm of the embryo, the same cannot be said of the peripheral nerve
trunks. These structures arise from the mesoblastic reticulum already
described (Sedgwick, _Quart. Journ. Mic. Sci._ xxxvii. 92). Inasmuch as
this reticulum is perfectly continuous with the precisely similar though
denser tissue in the ectoderm and endoderm, it may well be that a
portion of the nerve trunks should be described as being ectodermal and
endodermal in origin, though the bulk of them are undoubtedly formed
from that portion of the reticulum commonly described as mesoblastic.
But, however that may be, the tissue from which the great nerve trunks
are developed is continuous on all sides with a similar tissue which
pervades all the organs of the body, and in which the nuclei of these
organs are contained.
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