The cassava plant, Manihot esculenta, grows exceptionally well in low
fertility and drought prone environments, but the mechanisms that allo
w this growth are unknown. Earlier, and sometimes contradictory, work
speculated about the presence of a C4-type photosynthesis in cassava l
eaves. In the present work we found no evidence for a C4 metabolism in
mature attached cassava leaves as indicated i) by the low, 2 to 8%, i
ncorporation of (CO2)-C-14 into C4 organic acids in short time periods
, 10 s, and the lack of C-14 transfer from C4 acids to other compounds
in (CO2)-C-12, ii) by the lack of C4 enzyme activity changes during l
eaf development and the inability to detect C4 acid decarboxylases, an
d iii) by leaf CO2 compensation values between 49 and 65 mul of CO2 l-
1 and by other infrared gas exchange photosynthetic measurements. It i
s concluded that the leaf biochemistry of cassava follows the C3 pathw
ay of photosynthesis with no indication of a C3-C4 mechanism. However,
cassava leaves exhibit several novel characteristics. Attached leaves
have the ability to effectively partition carbon into sucrose with ne
arly 45% of the label in sucrose in about one min of (CO2)-C-14 Photos
ynthesis, contrasting with 34% in soybean (C3) and 25% in pigweed (C4)
. Cassava leaves displayed a strong preference for the synthesis of su
crose versus starch. Field grown cassava leaves exhibited high rates o
f photosynthesis and curvilinear responses to increasing sunlight irra
diances with a tendency to saturate only at high irradiances, above 15
00 mumol m-2 s-1. Morphologically, the cassava leaf has papillose epid
ermal cells on its lower mesophyll surface that form 'fence-like' arra
ngements encircling guard cells. It is proposed that the active synthe
sis of sugars has osmotic functions in the cassava plant and that the
papillose epidermal cells function to maintain a healthy leaf water st
atus in various environments.