Subject: Herpetological collection
Diana Ruby-Sanderson <dlrs [at] rmh__com> writes >My husband has worked with preserved herp specimens for about 20 >years now, some as old as late 19th century. He advises that >changing out formalin will not hurt the specimens and that you >should use 50% isopropyl alcohol (70% is too high a concentration >and may dry them out.) With regard to rehydrating dry >specimens--rinse them well in cool, running water to flush the >residual formalin and then soak them in running water for a least 24 >hours before placing them in the 50% alcohol. Although the above message is the "traditional" response to such an inquiry, I believe that there are some better solutions to the problems. Specimens in formalin are normally in "10% formalin" which is really about 3.5% formalin and 96.5% water. To rinse the specimens in water and then move them abruptly into alcohol will cause a rapid hydration-dehydration cycle, which is structurally hard on the tissues. Studies have shown that you will get less structural damage to the specimens if you stage them from the formalin through 35%, then 55% and then 70% ethyl alcohol. Most of the formalin will be washed out during this process. You can test the solution for trace amounts of formalin with commercially available aldehyde test strips or make your own. Ethyl alcohol is highly recommended over isopropyl alcohol. All alcohol will cause specimen shrinkage, but isopropyl has been shown to cause significantly more shrinkage than ethanol. Also, isopropanol is twice as toxic as ethanol, and many people are bothered by its fumes. Rehydrating completely dehydrated fluid preserved specimens is problematic. If the specimens have completely dehydrated, they are probably best left in that state. Rehydration is likely to weaken them further, as it will cause further tissue damage. If the specimens are not yet completely dehydrated, then you should try gently rehydrating one or two via slow steps from water to 70% ethyl alcohol. The use of a surfactant may aid rehydration, but will cause chemical changes in the tissue. I have discussed these issues at greater length and provide a bibliography on this subject in "Storage of Fluid-Preserved Collections," pp. 161- 186 in Carolyn L. Rose, Catharine A. Hawks, and Hugh H. Genoways (editors) 1995. Storage of Natural History Collections: A Preventive Conservation Approach, published by the Society for the Preservation of Natural History Collections. John Simmons Division of Herpetology Natural History Museum University of Kansas Lawrence, Kansas *** Conservation DistList Instance 12:61 Distributed: Wednesday, January 27, 1999 Message Id: cdl-12-61-001 ***Received on Monday, 25 January, 1999