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RGR and net assimilation rate (growth per unit leaf area) of 24 C3 species ( Poorter and Remkes, 1990 ), suggesting that greater biomass partitioning into leaf area, and not higher photosynthetic rates, was the mechanism leading to higher RGR

), we measured the DM and leaf area of the remaining five seedlings in each treatment group. We calculated the relative growth rate (RGR, d −1 ), net assimilation rate (NAR, g·m −2 ·d −1 DM basis), and leaf area ratio (LAR, m 2 ·g −1 ) after

were calculated. From the dry weights and leaf area data, net assimilation rate (NAR), leaf area ratio (LAR), and relative growth rate (RGR) were calculated according to Evans (1972) . To calculate NAR, LAR, and RGR, plants within the initial and

of net assimilation rate (A) to increasing PPF for sun and shade leaves of ‘Pawnee’ pecan trees through the 2007 growing season. Data are average ± se (n = 5); curves were fitted according to Hanson et al. (1987) . Arrows indicate 95% of maximum

Poorter, H. Remkes, C. 1990 Leaf area ration and net assimilation rate of 24 wild species differing in relative rate Oecologia 83 553 559 Prinsen, E. Chriqui, D. Vilaine, F. Tepfer, M

. 1990 Leaf area ratio and net assimilation rate of 24 wild species differing in relative growth rate Oecologia 83 553 559 Pramuk, L.A. Runkle, E.S. 2005 Photosynthetic daily light integral during the seedling stage influences subsequent growth and

1036 1043 Watson, D.J. 1947 Comparative physiological studies on the growth of field crops: I. Variation in net assimilation rate and leaf area between species and varieties, and with and between years Ann. Bot. (Lond.) 11

period between the two measurements. Net assimilation rate (NAR) was calculated as RGR divided by LAR during the period. Leaf weight ratio (LWR) was calculated as LAR divided by SLA. Results Effect of breeding in Dutch cultivars. Harvest of fruit was

assimilation rates and relative growth rates, while those from selected provenances in Utah had high leaf area ratios ( Bsoul et al., 2006 ). Our objective was to compare drought responses of bigtooth maples indigenous to locations in Texas, New Mexico, and

ascribed to leaf expansion that compensates for a reduced net assimilation rate, thus resulting in an increased photosynthetic capacity per plant ( Adams and Langton, 2005 ; Solhaug, 1991 ). Moreover, even though leaves and tillers of different cool