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LIKE FLOCK
osmium tetroxide buffered with veronal acetate according to Rhodin
(1954)l was applied in situ with a pipette. The organ was then dissected
free with its bony capsule, rinsed in Ringer, and dehydrated with 70%
alcohol. When appropriate areas had been exposed for scanning microscopy the tissue was frozen in liquid propane at -192°C and freezedried. After mounting with glue on metal holders the specimens were
covered with gold by vacuum evaporation and examined in a Cambridge
Stereoscan microscope. A similar procedure applies to epidermal lateral
line organs which were taken from the salamander, Necturus m u l o s u s .
Specimens for transmission electron microscopy were fixed in osmium
tetroxide, dehydrated in alcohol, embedded in Epon ( Luft, 1961 ) ,
sectioned in an LKB Ultrotome, and examined in a Siemens Elmiskop I.
B. Canal Organs
The sensory area is located at the bottom of a bony half-cylinder
( Fig. 1). At this point the lumen of the canal is narrowed by the presence
of a septum; here the cupula reaches its maximum height and partially
occludes the lumen. If volume displacement occurs between the two
Fig. 3. Bundles of sensory hairs project from the sensory surface.
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