VII. Summary and Conclusions
to the next indicate developmental changes that allow a
more accurate interpretation of real events (the fi rst 6 data
points in Figure 32 graphs). These quantitative data,
when combined with the qualitative evidence in the pho-
tographs, allow the construction of timetables of develop-
mental events among neuronal populations in the spinal
cord as shown in Table VII-1.
Figures 34 through 37 feature pie-charts showing
relative changes in the areas of varous components of the
spinal cord throughout its development. The problems
associated with fi xative, cutting planes, section thickness,
and staining types are much less relevant here. Figures
34 and 35 look at the entire range of development from
GW4.0 to the 4th postnatal week. Figures 36 and 37 look
at the changes in maturation of cervical through sacral
levels in 6 specimens from GW8.5 to the 4th postnatal
month.
Finally, Table VII-2 shows a semi-quantitative
analysis of the sequential steps in myelination in several of
the major fi ber tracts in the spinal cord at the level of the
cervical enlargement. These events can be used to make
some generalizations about myelination sequences in fi ber
tracts, not only in the spinal cord, but throughout the cen-
tral nervous system. These conclusions are explained in
the caption of Table VII-2.
This section features a quantitative summary of the
major developmental events that have been qualitatively
demonstrated in photographs of the spinal cord at imma-
ture through mature stages. In order to compare the com-
plete timetable of development, the cervical level is dealt
with most completely because that level is illustrated at all
ages. First, absolute changes in area are discussed, fol-
lowed by relative changes in area. Finally, a semi-quan-
titative approach using myelin staining density is used to
determine myelination sequences in various fi ber tracts.
Figures 32 and 33 show progressive changes in
area of various components of the spinal cord in absolute
values (mm^2 ). It is important to note that the absolute
values are based on a single specimen at each age; these
specimens were collected over a period of several years,
were preserved with different fi xatives, and were not all
cut at the same thickness or in exactly the same plane.
All of these factors contribute to “noise” in the data, and
the graphs are not smooth progressions from one age to
another. The time when most noise in the data exists is
between GW4.0 and GW6.8 in the fi rst trimester. Nine
specimens from this period are shown in Plates 2 through
- Fortunately, six of these specimens are from the Minot
Collection, where the fi xative is constant and the cutting
plane is more regular between specimens. When all of the
specimens in the Carnegie Collection are removed from
the data, the changes in absolute areas from one age