Maximum crop growth rate (_<max>CGR) was examined for seasonal regrowth in the pure swards of alfalfa (Medicago sativa L., Du Puits) and ladino clover (Trifolium repens L., Pajbjerg Milka), grown under well fertilized and managed conditions with four times of defoliations, and the correlations of _<max>CGR and net assimilation rate (NAR) with several growth attributes in optimal LAI (_<opt>L) period were determined. NAR was expressed as the following equation revised from those of IWAKI (1958). NAR=(a-γ)-γ_n/SLA-R・(C/F)・(1/SLA)…equation (3), in the text. Here, (a-γ) is apparent photosynthetic rate of canopy leaves on leaf area basis in the daytime, γ_n respiratory rate during night canopy leaves on dry weight basis and R respiratory rate of non-photosynthetic organs on dry weight basis. Other symbols are given in the explanation of table 1. The methods for measurements of dry matter production, stratified clipping for light attenuation (extinction) coefficient (K), solar radiant flux density (S) are the same as OKUBO et al (1969). For measurement of chlorophyll content on leaf area basis (ChA), the canopy was cut with the stratified clip method into four or five layers from the top to the bottom and weighd for fresh leaf weight. Duplicate fresh materials of 2-4g were samlped for chlorophyll content, 10g for moisture content and about 10g for leaf area measurement, from which the chlorophyll content on leaf area basis (ChA), that on dry weight basis (ChW) and specific leaf area (SLA) were calculated for each of leaf layers of a canopy. For the calculation of CI, the chlorolpyll amount of each leaf layer was once determined individually, summed it to the total chlorophyll amount of leaves per unit ground area (CIL ; leaf part of CI), and added stalk chlorophll (CIS ; stalk part of CI) to the CIL into the CI for a whole canopy. The average ChA of a whole canopy leaves was determined by dividing the CIL by the LAI. Other procedures were approximately the same as BROUGHAM (1960), but the equations for chlorophyll determination by ARNON (1949) were corrected as the equation 1 in the text because there were found some slight mistakes in ARNON's equations. 1._<max>CGR attained to the highest in spring growth (exactly in June) in alfalfa and in midsummer growth in ladino clover at the value of 20 and 21g/m^2/day, respectively, among those of four seasons. _<max>CGR during autumn growth period was the lowest in both species at the value of 12.1 and 5.8g/m^2/day in alfalfa and ladino clover swards, respectively. These variations in _<max>CGR depended more on the NAR than on the _<opt>L in the growth of four seasons. Since the solar radiation for the period of _<opt>L in autumn growth was very low, one thirds of that in spring, the low values in _<max>CGR, NAR and _<opt>L also might be partly caused by the low level of the solar radiation. 2. The highest ChA among the four seasonal growth was observed in June for alfalfa sward at the value of 4.68mg/dm^2 of leaf surface and in August for ladino clover of 4.68mg/dm^2 also. The lowest was found in autumn sward at 2.94 and 2.96mg/dm for each species. This variation in ChA was closely proportional to the _<max>CGR and the NAR. 3. The _<max>CGR significantly correlated positively to ChA (r=0.93), S (0.74) and T (0.81) and negatively to C/F ratio (-0.75). The correlation coefficient of NAR with ChA only attained to significant level among the several growth attributes (table 2). Partial correlation of the _<max>CGR showed a significant value to ChA and K, and the correlation of the NAR was significant only in case with ChA (table 3). ChA showed a simple correlation significantly with S, T and C/F, and a partial correlation with S and K. 4. Photosynthetic rate under saturated light for a single leaf, taken from various depth within a canopy around _<opt>L
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To ascertain the dependence of maximum crop growth rate (_<max>CGR) and net assimilation rate (NAR) upon chlorophyll content of leaf surface in the canopy having a nealy optimal LAI, as seen in the previous investigation, crop growth rate was measured in the alfalfa swards (Medicago sativa L., Du Puits) with four plant densities. The plots with four different level of density were coded as D1>D2>D3>D4 (see the explanation of fig.1). Several times of the measurements of dry matter growth both for the top and underground organ were set out when the canopy attained to 80% light interception at the ground level and continued at one-week intervals for each of the densities. Around the optimal LAI, two times of the measurements with stratified clip method were also carried at the intervals of a week at each density plot in order to determine the light extinction coefficient (K). The vertical changes in chlorophyll content and specific leaf area within a canopy, which was divided into 4〜5 leaf layers, were also measured. Other details in the method for CGR and chlorophyll measurements were the same as the previous papers (OKUBO et al, 1969, 1975a). Changes in photosynthetic rate under dim light (55, 100, and 150cal/dm^2/hr, 400〜700mμ) with leaf age were also determined for alfalfa leaves (Du Puits). The leaf materials were taken from various positions of the plants grown in artificial community, which were planted individually on a peat soil pot and arranged with space of 25×25cm in a glasshouse, and they had been marked on the day of leaf unfolding as leaf age zero. Initial slope of light-photosynthesis curve was calculated as the ratio of gross photosynthesis to incident visible light on energy basis ; the maximum energy efficiency (φ0). Apparatus used was the same as those in the work by GABRIELSEN et al (1959). Chlorophyll determination method was seen in the previous papers (OKUBO et al, 1964, 1975a) Symbols used were given in the explanation of fig.1. 1. Variation in _<max>CGR was observed among the different levels of plant density of alfalfa sward, and it obviously depended more on CI than on _<opt>L (fig.2). Since the CI at this stage can be shown as Cl=_<opt>L×ChA+stalk's chlorophyll and there was not so much difference among the values of _<opt>L, this dependence on CI means that the _<max>CGR and the NAR had close relations with chlorophyll content on leaf area basis (ChA per LAI) at the stage of _<opt>L for each canopy at each density, although solar radiation and C/F ratio showed relations more or less to the _<max>CGR or the NAR (fig.3). 2. ChA of a canopy leaves increased with growth and attained once to the highest level at the growth stage of _<opt>L (at 90〜95% light interception, exactly) followed by a decrease again at excess LAI. ChA measured for each leaf layer with different depth in a canopy showed at most 4.0〜5.0mg/dm^2 at the period of _<opt>L and were mostly below 4.0mg/dm^2 in the canopies before the _<opt>L (fig.4). 3. Photosynthetic rate under dim light increased with leaf age to the highest on 15-20th day from unfolding and decreased. ChA of the leaf showed approximately the same time course as the photosynthesis. The initial slope of the light-photosynthesis curve on energy basis (φ0) showed a close correlation with ChA in the range of 1.0〜5.0mg/dm^2 (fig.5, fig.6). 4. The dependence of _<max>CGR and NAR on ChA shown in the previous paper (OKUBO et al, 1975a) would be caused by the facts that the variation of photosynthetic activity occurred with aging and mutual shading of canopy leaves followed by changes in microenvironmental condition, especially in light, and that the change of the activity was apparently observed in terms of ChA in the canopy at _<opt>L. But the ChA as a weak light factor also must have contribute partly to the close correlation among _
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