Section-Cutting: A Practical Guide to the Preparation and Mounting of Sections for the Microscope, Special Prominence Being given to the Subject of Animal SectionsMarsh, Sylvester
Science
Section-Cutting: A Practical Guide to the Preparation and Mounting of Sections for the Microscope, Special Prominence Being given to the Subject of Animal Sections
Marsh, Sylvester
Microscopy; Microscopy -- Technique
28. _Cartilage._—The method to be employed in the preparation of
cartilage will entirely depend upon the nature of the staining agent, to
the action of which the sections are to be submitted. Thus, if the
elegant _gold method_ is to be followed, it is necessary that the
cartilage should be perfectly fresh; whilst if any of the other staining
agents are to be employed the tissue may have been previously preserved
in alcohol. An excellent object on which to demonstrate the gold process
is to be found in the articular cartilage of bone. It is a very easy
matter to obtain from the butchers the foot of a sheep which has just
been killed. The joint is to be opened, and the bones dissociated, when
they will be seen to have their extremities coated with a white
glistening membrane—this is the _articular cartilage_. Exceedingly thin
slices must be at once cut from it, and as only small sections are
required, a sharp razor may be used for the purpose, the blade being
either dry or simply wetted with distilled water. The sections as cut
are to be transferred to a small quantity of a half per cent. solution
of chloride of gold in a watch glass. Chloride of gold may be purchased
in small glass tubes hermetically sealed, each tube containing 15
grains, and costing about 2s. If, however, the student requires only a
small quantity of the staining fluid he need not be even at this small
expense, for as photographers for the requirements of their art always
keep on hand a standard solution of chloride of gold of the strength of
one per cent., a little of this may readily be obtained, and diluted to
the required degree. After the sections have been exposed to the action
of the staining fluid for about ten minutes they may be transferred to a
small beaker of distilled water, and exposed to diffused light for about
twenty-four hours, when they must be mounted in glycerine (§ 16).
Sections of cartilage may also be examined, without being stained, in
which case the field of the microscope should be only very feebly
illuminated. Or carmine staining (§ 14) may be resorted to—these
sections show well in glycerine, or if the staining be made very deep,
even Canada balsam may be employed, and with fair results.
Public-domain text, read in full here on John Shaqi.
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