Subject: Rehydrating invertebrate specimens
In Conservation DistList, Instance: 11:39, October 23, 1997 I wrote Kathy Hall <kathyhall<-a t->mail< . >utexas< . >edu> >I'm an objects conservator at Texas Memorial Museum. One of our >curators just asked me about what would be the best way to >rehydrate specimens from a collection of cave invertebrates >which unfortunately dried out. I understand that these types of >specimen are difficult to rehydrate due to the chitinaceous >exterior. This is the summary posted to nhcoll. Thanks everyone! A summary of the replies on this question: Extra References: Marhue, L. 1983. Techniques to restore dried-up invertebrate specimens. In: Proc. of the 1981 Workshop on the Care and Maintenance of Natural History Collections, edited by D.J.Faber, Syllogeus no.44: 175-177. Gives concentrations and soaking times for two different treatments;- the propylene glycol technique (50% solution for 24 hours, recommends not using ethylene glycol due to toxicity), and trisodium phosphate (0.5% overnight). Both found to be effective, no conclusions drawn as to best method. Also discusses using a few drops of surfactant in water (not tried but also said to be a successful method). Vogt, K.D. 1991. Reconstituting Dehydrated Museum Specimens. Curator 34:125-131. A response to problems with the trisodium phosphate (TSP) method with larger vertebrate specimens which can't be boiled and which would need impractically long soaking times. Describes a method which involves first soaking in a weak solution of acetic acid (to aid in disruption of the cell membrane and water transport across it), and then in TSP. The acetic acid will also act to inhibit microbial growth. This reduces soaking times. Probably not useful for calcareous invert. specimens, though. Also: Thompson, Thompson and Drummond. 1966., Crustaceana 10, p109. Also discusses the ethylene glycol technique. Holm, Ake. 1978. Om Carl Clerk Spindelsamling. Fauna och Flora, 73(5):201-205. On reclaiming the oldest spider collection in the world (thanks to James Cokendolpher for the translation) -specimens were first wet with drops of ethylacetate and then 50% alcohol added, after a few days this replaced with 80%. [I assume this works in the same way as using acetic acid]. In addition: Several people said they had used the TSP method, and were happy with the results, one person recommended leaving the specimens as they are (dry), one person mentioned contacting the SPNHC Fluid Assessment Subcommittee, and one person had tried rehydrating fish larvae using ethanol or 3% formalin with mixed results (no change in ethanol, some specimens absorbed some fluid in formalin but were still mis-shapen). Also mentioned was the possibility of using a 75:25 mix of isopropyl alcohol in distilled water and heating in a microwave. (I would think that using a microwave is not a good heating technique as it is so very uncontrolled). One person also recommended adding glycerin to the final ethanol solution -so that specimens will remain flexible if they dry out. Levi*, however, does not recommend this, saying that it is messy and will encourage mould growth if they dry out again ("The Care of Alcoholic Collections of Small Invertebrates", Herbert W. Levi, Systematic Zoology, vol 15, #3, September 26, 1966). So.. I guess that we will try using TSP or a surfactant on a small batch of test specimens, at as low concentrations and for as short a time as possible, soaking to remove residue, refixing, and then taking them up to 70% ethanol in steps. Hopefully this will give some idea on the best way to treat the rest of the specimens. Kathy Hall *** Conservation DistList Instance 11:45 Distributed: Monday, November 17, 1997 Message Id: cdl-11-45-006 ***Received on Monday, 10 November, 1997