MICROSCOPE SLIDE OR SEM STUB PREPARATION

OCTOCORAL SCLERITES OR OTHER INVERTEBRATE SPICULES

Compiled by Gary Williams and Courtney Mattison

1. Put a small amount of tissue (about 5 cubic millimeters or less) in a circular watch glass (ca. 30-35 mm diameter).

2. Add 2 drops of common household bleach (sodium hypochlorite - NaOCl) to the tissue, using an eyedropper or pipette.

3. Macerate for about 5 minutes until a sufficient quantity of sclerites have been dissociated from the tissue sample. Remove pieces of excess tissue.

4. Fill the watch glass with clean water. Allow all of the sclerites to sink to the bottom, then pipette off the liquid. Repeat this washing process one or two more times.

5. Fill the watch glass with 95% ethanol. Allow all the sclerites to sink to the bottom, then carefully pipette off the fluid. Fill the watch glass with 95% ethanol once again. A current generated by a pipette on the inside edge of the watch glass will result in sclerites concentrated in the center.

6. Allow the sclerites to sink, then pipette a quantity of sclerites in ethanol from the watch glass to the surface of an SEM stub or the center of a glass microscope slide.

7. Air-dry completely until the sclerites look like dry powder on the microscope slide or SEM stub.

8. FOR MICROSCOPE SLIDES: Under a fume hood, add 5 drops of mounting medium such as CYTOSEAL* to the sclerites on the slide.

9. FOR MICROSCOPE SLIDES: Drop a square cover slip over the sclerites and mounting medium. Allow the slide to set on a flat surface for several days to dry.

10. FOR MICROSCOPE SLIDES: Glue a square label printed from a computer (using font 7) onto the right side of the slide. Include scientific name, locality, museum collection catalog number, and where on the specimen the sclerites are from (surface coenenchyme, interior coenenchyme, polyp walls, calyces, anthocodiae, tentacles, crown and points, etc.).

-----------------------------

* NOTE: for temporary slides, use GLYCEROL instead of PERMOUNT or CYTOSEAL.