“…Supranasal sacs of both specimens were dissected out, dehydrated and cleared in alcohols and xylene, embedded in paraffin, and sectioned at 20 and 30 µm. A few of the 20 µm sections were later shaved to produce two sections 8 µm thick (Silver, 1996). Sections were stained with Winkelman's (1960) method for nerve endings, Kiernan's (1990) physical developer method for axons, Ehrlich's acid hematoxylin (Lillie, 1954), toluidine blue (Lillie, 1954), azure A eosinate (Lillie, 1954), PAS (Lillie, 1954), colloidal iron (Mowry, 1958), paraldehyde fuchsin and alcian blue (Spicer and Meyer, 1960), and Cason's trichrome (Kiernan, 1990).…”