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Net and gross production rates were determined in the field at light intensities above 20,000 lux for 45 species of marine macroalgae from four different environments in southwestern North America. Thin sheetlike and finely branched thallus-forms showed greater rates than other forms. A morphological form more suited to efficiently utilize light energy and obtain nutrients is clearly related to the differences measured. There was a close relationship between dry weight as well as two-dimensional thallus area and photosynthetic performance for macrophytes having relatively large surface areas (z.e., thin and finely branched forms). However, the productivity values for the range of coarsely-branched to encrusting forms were in closer agreement with respect to thallus area than with respect to dry weight.

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Predictions of an evolutionary model were examined for 43 tropical macroalgae using a functional‐form group approach. The ranking from high to low primary producers (Sheet‐ and Filamentous‐Groups > Coarsely Branched‐ and Thick Leathery‐Groups > Jointed Calcareous‐ and Crustose‐Groups), and data from the literature, support the hypothesis that persistent forms which allocate resources for environmental resistance, interference competition or antiherbivory defenses do so at the cost of lower primary production rates. The results for percent thallus lost to fish grazing over a 24 h period support the hypothesis that members of the Thick Leathery‐, Jointed Calcareous‐ and Crustose‐Groups have evolved antipredator defenses, with a tendency for decreasing herbivore resistance toward the Sheet‐ and Filamentous‐Groups. The most heavily‐calcified species (e.g. crustose corallines) ranked among the most grazer resistant as did the thick rubbery or leathery species. The ranking of functional‐form group means for resistance to predation was as follows: Filamentous‐Group (62% lost‐24 h−1), Sheet‐Group (42%), Coarsely Branched‐Group (33%), Jointed Calcareous‐Group (10%), Thick Leathery‐Group (7%) and Crustose‐Group (0%), in accordance with the hypothesis. The algal groups generally showed an increase in mean penetration toughness from filaments (<200 g‐cm−2 to shear thallus) to sheets (216 g·cm2), coarsely branched forms (328 g·cm−2) and thick leathery species (1800 g·cm−2) in agreement with the predictions of the model. Contrary to earlier findings, there was no consistent gradation between the first four groups (i.e. fleshy algae) based on calorific values. However, in partial support of the functional‐form model, a seven‐fold difference was noted when the mean for these groups (1.7 kcal·g−1) was compared with that of the Jointed Calcareous‐ and Crustose‐Groups (0.2 kcal·g−1. The functional‐form group approach appears to have powerful capabilities in that it can indicate important morphological‐metabolic‐ecological interactions in a given community, where the macroalgae are known, without the need to examine each population in detail and without being constrained to a specific habitat or geographical region.

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The discovery of abundant autotrophic macrophytes living below 200 meters indicates their importance to primary productivity, food webs, sedimentary processes, and as reef builders in clear oceanic waters. Estimates concerning minimum light levels for macroalgal photosynthesis and macrophytic contributions to the biology and geology of tropical insular and continental borderlands must now be revised.