A comprehensive canopy productivity model was built to study the produ
ctivity of a primary salt marsh grass, Spartina alterniflora, in Georg
ia, USA. The canopy model was unique in employing plant demographic da
ta to reconstruct canopy profiles and dynamics, which showed many grow
th processes that are otherwise difficult to discern in the held. By l
inking canopy dynamics and leaf photosynthesis, the net total primary
productivity of S. alterniflora in a Georgia salt marsh was estimated
to be 1421, 749, and 1441 g C m(-2) yr(-1) for the tall, short, and N-
fertilized short populations respectively. These estimates are reasona
ble in terms of the physiological capacity of S. alterniflora and well
below the range of 3000-4200 g C m(-2) yr(-1) as reported by some rec
ent harvest studies, Our detailed analysis suggested the net total pro
ductivity of S. alterniflora might be greatly overestimated in the pas
t. This is mainly because of 1) failure to consider the translocation
of photosynthate between aboveground and belowground pans, and 2) poss
ible overestimates of belowground production. We estimated the net bel
owground production to be 872, 397, and 762 g C m(-2) yr(-1) for the t
all, short, and N-fertilized populations respectively. After receiving
nitrogen fertilizer, the net leaf carbon fixation in the short popula
tion increased from 1489 to 2487 g C m(-2) yr(-1); and our simulation
showed the contribution of elevated leaf N to this increase was small,
21%, compared with that of increased leaf area, 79%. Both tall and sh
ort populations allocated ca 48-49% of their annual gross leaf carbon
fixation to belowground structures. Nitrogen enrichment caused more al
location to aboveground parts in the short population, mainly for incr
easing leaf area. The canopy model assumed that there was no leaf phot
osynthesis under tidal submergence, but if this assumption was relaxed
, then leaf carbon fixation might increase 7-13% for different S. alte
rniflora populations. Although this research focused only on a salt ma
rsh species, our general approaches, especially the coupling of leaf p
hysiology with the reconstructed canopies, should be applicable to the
study of production processes of many other plant populations.