The Microscope. Its History, Construction, and Application 15th ed.: Being a familiar introduction to the use of the instrument, and the study of microscopical scienceHogg, Jabez
History
The Microscope. Its History, Construction, and Application 15th ed.: Being a familiar introduction to the use of the instrument, and the study of microscopical science
Hogg, Jabez
Microscopy; Natural history
_Löffler’s Method._--Add together aqueous solutions of ferrous-sulphate
and tannin (twenty per cent.) until the mixture turns a violet-black
colour, then add three or four cc. of a one-in-eight aqueous
solution of logwood; a few drops of carbolic acid may be added
before transferring to a stoppered bottle; that is the mordant. The
dye consists of 1 cc. of a one per cent. solution of caustic soda,
added to 100 cc. of aniline water, in which four or five grammes of
either methyl-violet, methylene blue, or fuchsine, are dissolved. A
cover-glass preparation is made in the usual way, then the film is
covered with mordant, and cover-glass held over flame until steam
rises, the mordant is then washed off with distilled water. The stain
is filtered and a few drops allowed to fall on film, after a few
minutes the cover-glass is again warmed until steam rises. The stain is
then washed off with distilled water, and the preparation is ready to
be mounted for examination.
As Löffler’s process is somewhat complicated, a modification has been
said to afford more satisfactory results. A specimen is taken from
a recent gelatine culture and diluted with water. A little of the
fluid is then transferred to a warm cover-glass by means of a pipette
and allowed to dry, after which a drop of the following mordant is
applied:--Aqueous solution of tannin (twenty per cent.), ten cc.; cold
saturated solution of ferrous sulphate, five cc.; saturated solution of
fuchsine in absolute alcohol, one cc. The cover is next heated gently
for a short time until vapours are given off, then washed carefully.
This process is repeated two or three times, and the specimen washed
after each application. Subsequently, staining is effected by means
of Ziehl’s fuchsine solution, the cover is afterwards warmed once or
twice for about fifteen seconds, then washed, and the specimen examined
in water to ascertain if the colour is sufficiently intense. If
satisfactory, the preparation may then be dried and finally mounted in
Canada balsam or dammar.
_Preservation of Preparations._--After examining a cover-glass
preparation with an oil-immersion objective the cedar oil must be
carefully wiped off, and the slide set aside for the Canada balsam to
set. At a convenient time these preparations should be sealed with a
ring of Hollis’s glue.
Bacteria in Sections of Tissues.
_Method of Hardening and Decalcifying Tissues._--To harden small
organs, such as the viscera of a mouse, they should be placed on a
piece of filter-paper at the bottom of a small wide-mouthed glass jar,
and covered with about twenty times their volume of absolute alcohol.
Larger organs are treated in the same way, but must be cut up into
small pieces. Müller’s fluid, methylated spirit, or formalin may be
used.
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