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Ecophysiological comportment of the tropical CAM‐tree Clusia in the field
Author(s) -
BALL E.,
HANN J.,
KLUGE M.,
LEE H. S. J.,
LÜTTGE U.,
ORTHEN B.,
POPP M.,
SCHMITT A.,
TING I. P.
Publication year - 1991
Publication title -
new phytologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.742
H-Index - 244
eISSN - 1469-8137
pISSN - 0028-646X
DOI - 10.1111/j.1469-8137.1991.tb00012.x
Subject(s) - crassulacean acid metabolism , malic acid , botany , chemistry , xylem , citric acid , starch , horticulture , biology , photosynthesis , biochemistry
summary Measurements were performed on leaves of Clusia rosea Jacq. trees in the moist central mountains (330 to 365 m above sea level) and at the dry south coast of St John Island (US Virgin Islands, Lesser Antilles). Seedlings of C. rosea were also studied in the central hills. During the study period (March 1989) all trees showed crassulacean acid metabolism (CAM), in which net CO 2 uptake extended for a remarkably long time in the morning (phase II of CAM: until about 11 to 12 h) and contributed about 1/3 of total net CO 2 ‐uptake. During the night (phase I of CAM) malic acid and citric acid were accumulated concurrently at a molar ratio of malic: citric acid of about 1.6. Internal recycling of respiratory CO 2 was 20% of total CO 2 fixed during the night. Water‐use‐efficiency (mol CO 2 taken up: mol H 2 O transpired) was 0.014 to 0.022. The pH of leaf‐cell sap at the end of the dark period was 2.85. This would still allow an H + ‐ATPase at the tonoplast to transport 2H + into the vacuole per ATP hydrolysed when operating near thermodynamic equilibrium. Free sugars, glucose and fructose, and starch were used as precursors for the CO 2 ‐acceptor phosphoenolpyruvate during the dark period; contributions of the two hexoses were about equal and together four‐times that of starch. Xylem tensions showed increases of up to 8 bar during day‐time. Leaf‐sap osmotic pressures did not change significantly; the trend was a small decline during day‐time. Among the seedlings, three different modes of photosynthesis were encountered, namely C 3 ‐photosynthesis in terrestrial and in epiphytic seedlings, continuous stomatal opening and CO 2 ‐uptake day and night in epiphytic seedlings, and CAM in seedlings growing in the tanks of Aechmea lingulata (L.) Baker.