Carbon Metabolism in Seagrasses: II. PATTERNS OF PHOTOS YNTHETIC CO2 INCORPORATION

Patterns of initial photosynthetic CO₂ incorporation were determinedfor some seagrasses and were related to activities of primarycarbon fixing enzymes, carbonic anhydrase activities, and ¹³Cvalues. According to the incorporation patterns, Cymodocea nodosa wasa C4 species while Thalassia hemprichli and Thalassodendronciliatum were C₃ plants. Halophila stipulacea showed an unusualincorporation pattern which could be viewed as intermediatebetween typical C₃ and C₄ pathways. The activity ratios of ribulose-l,5-bisphosphate carboxylase (RUBPcase) to phosphoenolpyruvatecarboxylase (PEPcase) were about 3 for Thalassodendron ciliatumand 1 for Cymodocea nodosa and Halophila stipulacea. The lattervalue, which is intermediate to ratios found in terrestrialC₃ and C₄ plants, may correlate with the incorporation patternsfound for Halophila stipulacea. Since the C₄ seagrass lackedthe Kranz anatomy, it may, in addition, point to a flexibleincorporation potential for these plants. The high ¹³C values found in these and other seagrasses didnot correlate with their photosynthetic pathways as in terrestrialplants. This discrepancy is probably due to a ‘closedsystem’ type of photosynthesis in which CO₂ is efficientlyutilized. The C₃ species which utilize CO₂ enzymatically must convertexogenous HCO-₃ to CO₂ internally. Even though carbonic anhydraseactivities were very low, conversion rates seemed to be sufficientfor high rates of photosynthesis. Since enzymatic fixation ratesapproached photosynthetic rates even at CO₂ saturation, thelimitation for these seagrasses to express their high photosyntheticpotential is most probably the HCO^–₃ uptake system.