Cucurbit Genetics Cooperative Report 7:14-16 (article
7) 1984
Effect of Length of Vegetative Phase on
Total Dry Matter Production and Its Partitioning
D.R. Ramirez and T.C. Wehner
Department of Horticultural Science, North Carolina State University, Raleigh, NC 27695-7609
The onset of fruit development usually determines the extent of
vegetative growth in crops. The length of both vegetative and
reproductive phases in the growth of plants have been claimed to
be important in determining yields in maize (Zea mays L.)
(4) and cereals (1). Inhibition of vegetative growth by fruit
development has been demonstrated in cucumbers (3). Assimilate
supply from source leaves could also be limiting growth (2).
Dry matter production depends basically on the amount of
photosynthetic leaf surface and the rate of carbon fixation
(photosynthesis) per unit of leaf area. Most of the variation in
yields of crop species was related to differences in rate of
increase in leaf area rather than differences in net assimilation
rate (5).
This experiment was aimed at determining the effect of an
increase in the length of the vegetative phase on total dry
weight production (a good estimate of net photosynthetic
capacity). A second consideration was the effect on Partitioning
of assimilates into source (leaves, stems) and sink (fruits)
tissues.
Methods. Plants of the cultivar Calypso were grown in pots in
the Horticultural Science greenhouses at the North Carolina State
University in Raleigh, NC, from Jan. 27 through April 11, 1983.
The experiment consisted of 4 flower removal treatments arranged
in a randomized complete block design with 4 replications.
Treatments consisted of the daily removal of female flowers for
0, 7, 14 and 21 days beginning when plants were 36 days old. The
following parameters were measured at harvest: fresh and dry
weights of leaves, stems and fruits; number of branches, leaves
and fruits; stem length; and leaf area.
Results. Total fresh and dry weight production was not increased
by increasing the length of the vegetative phase, but dry matter
and fresh matter partitioning were greatly modified (Tables 1 and
3). Removal of flowers for 14 and 21 days significantly
increased the percentage of dry and fresh weight that were
devoted to leaf and stem growth and decreased the dry and fresh
weight devoted to fruit growth. All flower removal treatments
resulted in an increase in the number of branches and leaves,
producing a larger plant (Table 2). Leaf area increased with
increased flower removal but was only significant for the 21 day
treatment. Flower removal for 7 days resulted in an increase in
the number of fruits per plant, and fresh and dry weights of
fruits (Tables 1 and 2), but the differences were not
significant. This lack of significance could be due to the fact
that fruit set was not uniform in the population of plants and
treatment differences could have been masked by this variability.
It seems that excessive vegetative development (as that obtained
by the 14 and 21 day flower removal) is detrimental for fruit
growth, as more assimilates are then diverted into unneeded leaf
and stem growth.
Table 1. Fresh and dry weight production as
affected by number of days of flower
removal.z |
Days of Flower
Removaly |
Fresh Weight Production (g) |
Dry Weight Production (g) |
Leaves |
Stems |
Fruits |
Total |
Leaves |
Stems |
Fruits |
Total |
0 |
65.7 |
65.3 |
726.7 |
857.7 |
8.2 |
4.0 |
29.3 |
41.4 |
7 |
69.6 |
72.0 |
761.4 |
903.0 |
8.6 |
4.4 |
30.6 |
43.7 |
14 |
84.3 |
90.8 |
665.0 |
840.1 |
10.4 |
6.4 |
25.5 |
42.1 |
21 |
115.4 |
113.6 |
635.3 |
864.2 |
13.9 |
8.7 |
19.4 |
42.0 |
LSD (5%) |
10.3 |
18.2 |
101.1 |
118.1 |
1.0 |
1.3 |
3.5 |
4.3 |
CV (%) |
8 |
13 |
9 |
9 |
6 |
14 |
8 |
6 |
zData are means over
four replications. |
yTreatments begun 36
days after planting. |
Table 2. Branch number, leaf number, fruit
number, stem length and leaf area as affected by number of days
of flower removal.z |
Days of Flower Removaly |
Branch number |
Leaf number |
Fruit number |
Stem length (cm) |
Leaf area (cm2) |
0 |
0.0 |
16 |
2.5 |
110 |
3250 |
7 |
2.5 |
25 |
3.0 |
119 |
3473 |
14 |
4.0 |
26 |
2.3 |
134 |
4134 |
21 |
7.0 |
39 |
2.8 |
159 |
5190 |
LSD (5%) |
2.0 |
4.6 |
0.7 |
36 |
897 |
CV (%) |
37 |
11 |
17 |
18 |
14 |
zData are means over
four replications |
yTreatments begun 36
days after planting |
Table 3. Distribution of fresh or dry matter in
plant parts as affected by the number of days of flower
removal.z |
Days of Flower
Removaly |
Distribution of Fresh Weight (%) |
Distribution of Dry Weight
(%) |
Leaves |
Stems |
Fruits |
Leaves |
Stems |
Fruits |
0 |
19.8 |
9.5 |
70.7 |
7.7 |
7.6 |
84.7 |
7 |
19.7 |
10.2 |
70.1 |
7.7 |
8.0 |
84.3 |
14 |
24.7 |
14.9 |
60.5 |
10.1 |
10.9 |
79.1 |
21 |
33.2 |
20.8 |
46.0 |
13.4 |
13.1 |
73.4 |
LSD (5%) |
1.9 |
3.0 |
4.5 |
0.9 |
1.6 |
2.0 |
CV (%) |
5 |
14 |
5 |
6 |
10 |
2 |
zData are means over
four replications. |
yTreatments begun 36
days after planting. |
Literature cited:
- Bingham, J. 1969. The physiological determinants of grain yield
in cereals. Agric. Prog. 44:30-42.
- Clifford, P.E. 1979. Source limitation of sink yield in mung
beans. Ann. Bot., N.S. 43:397-399.
- Denna, D.W. 1973. Effects of genetic parthenocarpy and
gynoecious flowering habits on fruit production and growth of
cucumber, Cucumis sativus L. J. Amer. Soc. Hort. Sci.
98:602-604.
- Hanway, J.J. and W.A. Russell. 1969. Dry matter accumulation in
corn (Zea mays L.) plants: comparisons among single cross
hybrids. Agron. J. 61:947-951.
- Watson, D.J. 1952. The physiological basis of variation in
yield. Adv. Agron. 4:101-145.