Mussel culture and the accumulation of domoic acid.

The cultured mussel industry of Prince Edward Island had never experienced a toxic disease problem until November of 1987. With the successful use of the long-line culture system, the yearly production of fresh mussels to the gourmet food market had risen to close to 3.2 million pounds (1.46 million kg) of product. The physiology of this sessile bivalve and its method of feeding and location in the estuary leave it prone to the accumulation of a widely distributed biotoxin. Eastern Prince Edward Island became the epicentre of domoic acid-intoxicated mussels as early as 10 November 1987 (retrospective samples) during an intense bloom of the diatom Nitzschia. Mussels were able to accumulate large amounts of the domoic acid with little effect on their own well-being. Despite being in low water temperatures (below 4 degrees C) and under thick ice cover, the levels of the toxin decreased and were undetectable in about 6 weeks. The following year the toxin was detected in much smaller amounts, and the levels of toxin accumulation demonstrated a variable lag time with the increase in concentration of Nitzschia available in the water column. The sales of Prince Edward Island cultured mussels have rebounded to about 140% of the pre-domoic acid crisis.

Feulgen, iron-propionocarmine and cupra-ammonium in preparing algal chromosomes for light microscopy.

A method for obtaining algal chromosomal preparations is described employing the Feulgen method for DNA staining, Fe-propionocarmine as an enhancing stain, and cupra-ammonium to remove cell wall material. Fe-propionocarmine applied as a gradient to the side provides cells stained with the Feulgen stain alone or with the Feulgen Fe-propionocarmine stain, thereby facilitating useful comparison. Where dilute the Fe-propionocarmine enhances nuclear staining without staining orthe organelles; where more concentration it also stains the nucleolus, spindle, spindle polar bodies, pyrenoid and protoplast. Treatment with cupra-ammonium, to remove polysaccharide wall material, followed by neutralization with propionocarmine, enables thinner squashes and better chromosome spreads without loss of differential staining. Preparations mounted in euparal are long-lasting.

STUDIES ON THE ALGAL CUTICLE(1).

A chemically resistant cuticle fraction was isolated from 5 phaeophycean, 1 rhodophycean, and 11 chlorophycean marine algae using acid treatment alone, or acid treatment followed by leaching in cupra-ammonium. In Cladophora rupestris and Chaetomorpha melagonium this fraction consists of several alternate microfibrillar and amorphous layers similar in appearance to those seen in innermost carbohydrate-rich regions and amount to about 1/10 or more of the cell wall thickness. In Porphyra umbilicalis and Padina vickersiae it is a single layer less than I µ thick, accounting for 1/50-1/100 of the cell wall in Porphyra, and 1/5-1/10 of the cell wall in Padina. The cuticle fractions of all 4 algae contain surprisingly large amounts of protein (about 70% in Cladophora and 80% in Porphyra). Similarities in the behavior of cuticles obtained from the other 12 species studied suggest that they may have a similar protein-rich composition.