Resistance Analysis of Nocturnal Carbon Dioxide Uptake by a Crassulacean Acid Metabolism Succulent, Agave deserti
Author(s) -
Park S. Nobel,
Terry L. Hartsock
Publication year - 1978
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.61.4.510
Subject(s) - crassulacean acid metabolism , phosphoenolpyruvate carboxylase , photosynthesis , carbon dioxide , botany , nocturnal , horticulture , chemistry , biology , ecology
Nocturnal CO(2) uptake by a Crassulacean acid metabolism succulent, Agave deserti Engelm. (Agavaceae), was measured so that the resistance properties of the mesophyll chlorenchyma cells and their CO(2) concentrations could be determined. Two equivalents of acidity were produced at night per mole of CO(2) taken up. The nocturnal CO(2) uptake became light-saturated at 3.5 mEinsteins cm(-2) of photosynthetically active radiation (400-700 nm) incident during the preceding day; at least 46 Einsteins were required per mole of CO(2) fixed. Variations in the daytime leaf temperature between 20 and 37 C had little effect on nocturnal CO(2) uptake. After the first few hours in the dark, the leaf liquid phase CO(2) resistance (r(liq) (CO(2) )) and the CO(2) concentration in the chlorenchyma cells (c(i) (CO(2) )) both increased, the latter usually reaching the ambient external CO(2) level at the end of the dark period. Increasing the leaf surface temperature above 15 C at night markedly increased the stomatal resistance, r(liq) (CO(2) ), and c(i) (CO(2) ).The minimum r(liq) (CO(2) ) at night was about 1.6 seconds cm(-1). Based on the ratio of chlorenchyma surface area to total leaf surface area of 82, this r(liq) (CO(2) ) corresponded to a minimum cellular resistance of approximately 130 seconds cm(-1), comparable to values for mesophyll cells of C(3) plants. The contribution of the carboxylation reaction and/or other biochemical steps to r(liq) (CO(2) ) may increase appreciably as the nighttime temperature shifts a few degrees from the optimum or after a few hours in the dark, both of which caused large increases in r(liq) (CO(2) ). This necessitates a large internal leaf area for CO(2) diffusion into the chlorenchyma to support moderate nocturnal CO(2) uptake rates by these succulent leaves.
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