Leaf water use in heterobaric and homobaric leafed canopy tree species in a Malaysian tropical rain forest

Verfasser / Beitragende:
[Y. Inoue, T. Kenzo, A. Tanaka-Oda, A. Yoneyama, T. Ichie]
Ort, Verlag, Jahr:
2015
Enthalten in:
Photosynthetica, 53/2(2015-06-01), 177-186
Format:
Artikel (online)
ID: 605481040
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024 7 0 |a 10.1007/s11099-015-0105-6  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s11099-015-0105-6 
245 0 0 |a Leaf water use in heterobaric and homobaric leafed canopy tree species in a Malaysian tropical rain forest  |h [Elektronische Daten]  |c [Y. Inoue, T. Kenzo, A. Tanaka-Oda, A. Yoneyama, T. Ichie] 
520 3 |a Tropical canopy tree species can be classified into two types by their heterobaric and homobaric leaves. We studied the relation between both leaf types and their water use, together with the morphological characteristics of leaves and xylem, in 23 canopy species in a tropical rain forest. The maximum rates of photosynthesis and transpiration were significantly higher in heterobaric leaf species, which also underwent larger diurnal variations of leaf water potential compared to homobaric leaf species. The vessel diameter was significantly larger and the stomatal pore index (SPI) was significantly higher in heterobaric than that in homobaric leaf species. There was a significant positive correlation between the vessel diameter, SPI, and maximum transpiration rates in all the studied species of both leaf types. However, there was no significant difference in other properties, such as leaf water-use efficiency, leaf mass per area, leaf nitrogen content, and leaf δ13C between heterobaric and homobaric leaf species. Our results indicate that leaf and xylem morphological differences between heterobaric and homobaric leaf species are closely related to leaf water-use characteristics, even in the same habitat: heterobaric leaf species achieved a high carbon gain with large water use under strong light conditions, whereas homobaric leaf species can maintain a high leaf water potential even at midday as a result of low water use in the canopy environment. 
540 |a The Institute of Experimental Botany, 2015 
690 7 |a bundle-sheath extension  |2 nationallicence 
690 7 |a Dipterocarpaceae  |2 nationallicence 
690 7 |a gas exchange  |2 nationallicence 
690 7 |a leaf morphology  |2 nationallicence 
690 7 |a wood density  |2 nationallicence 
690 7 |a BSE : bundle-sheath extension  |2 nationallicence 
690 7 |a DBH : stem diameter at breast height  |2 nationallicence 
690 7 |a D v : vessel diameter  |2 nationallicence 
690 7 |a E max : maximum transpiration rate  |2 nationallicence 
690 7 |a GCL : guard cell length  |2 nationallicence 
690 7 |a g s : stomatal conductance at P max  |2 nationallicence 
690 7 |a LMA : leaf mass per area  |2 nationallicence 
690 7 |a Narea : nitrogen per unit leaf area  |2 nationallicence 
690 7 |a Nmass : mass-based leaf nitrogen concentration  |2 nationallicence 
690 7 |a PIC : phylogenetically independent contrast  |2 nationallicence 
690 7 |a P max : maximum photosynthetic rate  |2 nationallicence 
690 7 |a PNUE : the ratio of CO2 assimilation rate to leaf organic nitrogen content  |2 nationallicence 
690 7 |a RGR : relative growth rate  |2 nationallicence 
690 7 |a SD : stomatal density  |2 nationallicence 
690 7 |a SPI : stomatal pore index  |2 nationallicence 
690 7 |a V d : vessel density  |2 nationallicence 
690 7 |a VPD : vapor pressure deficit  |2 nationallicence 
690 7 |a W d : wood density  |2 nationallicence 
690 7 |a WUE : intrinsic water-use efficiency  |2 nationallicence 
690 7 |a δ13C : stable carbon isotope ratio  |2 nationallicence 
690 7 |a ΔΨL : diurnal variation in the leaf water potential  |2 nationallicence 
690 7 |a Ψmid : leaf water potential at midday  |2 nationallicence 
690 7 |a Ψpd : leaf water potential at predawn  |2 nationallicence 
700 1 |a Inoue  |D Y.  |u The United Graduate School of Agricultural Sciences, Ehime University, 790-8566, Matsuyama, Japan  |4 aut 
700 1 |a Kenzo  |D T.  |u Forestry and Forest Products Research Institute, 305-8687, Tsukuba, Japan  |4 aut 
700 1 |a Tanaka-Oda  |D A.  |u Forestry and Forest Products Research Institute, 305-8687, Tsukuba, Japan  |4 aut 
700 1 |a Yoneyama  |D A.  |u The United Graduate School of Agricultural Sciences, Ehime University, 790-8566, Matsuyama, Japan  |4 aut 
700 1 |a Ichie  |D T.  |u Faculty of Agriculture, Kochi University, 783-8502, Nankoku, Japan  |4 aut 
773 0 |t Photosynthetica  |d The Institute of Experimental Biology of the Czech Academy of Sciences  |g 53/2(2015-06-01), 177-186  |x 0300-3604  |q 53:2<177  |1 2015  |2 53  |o 11099 
856 4 0 |u https://doi.org/10.1007/s11099-015-0105-6  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s11099-015-0105-6  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Inoue  |D Y.  |u The United Graduate School of Agricultural Sciences, Ehime University, 790-8566, Matsuyama, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kenzo  |D T.  |u Forestry and Forest Products Research Institute, 305-8687, Tsukuba, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Tanaka-Oda  |D A.  |u Forestry and Forest Products Research Institute, 305-8687, Tsukuba, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yoneyama  |D A.  |u The United Graduate School of Agricultural Sciences, Ehime University, 790-8566, Matsuyama, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ichie  |D T.  |u Faculty of Agriculture, Kochi University, 783-8502, Nankoku, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Photosynthetica  |d The Institute of Experimental Biology of the Czech Academy of Sciences  |g 53/2(2015-06-01), 177-186  |x 0300-3604  |q 53:2<177  |1 2015  |2 53  |o 11099