Volume 6
Issue 1
Agronomy
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Available Online: http://www.ejpau.media.pl/volume6/issue1/agronomy/art-01.html
RESPONSE OF SOME CULTIVATED PLANTS TO METHANOL AS COMPARED TO SUPPLEMENTAL IRRIGATION
Irena Zbieć, Stanisław Karczmarczyk, Cezary Podsiadło
Field and laboratory experiments aimed at the assessment of the impact of diluted methyl alcohol applied overhead 4-5 times in one-week intervals on growth and yield of tomato, bean, sugar beet, oil seed rape, as compared to supplemental irrigation. The photosynthetic activity was measured in situ with an LC-4 gas analyser. The crops when treated with methanol solutions yielded 20-30% higher than the control. The yield increases were comparable to those caused by supplemental irrigation. The increased biomass synthesis caused either by irrigation or methanol application was due to enhanced carbon dioxide assimilation, transpiration, leaf conductivity, and higher activity of nitrate reductase and alkaline phosphatase.
Key words:
methanol, irrigation, bean, sugar beet, tomato, oil seed rape.
INTRODUCTION
Production of biomass by plants depends to a great extent on environmental factors, such as water supply, air temperature, insolation, carbon dioxide concentration in the canopy. Numerous experiments have shown that by increasing the CO2 content in air, the crops yielded better [5], flowering was accelerated [6] and plants accumulated more carbohydrates [1]. Besford [2] who studied the effects of prolonged CO2 enrichment on the photosynthetic performance and Calvin cycle enzymes of tomato plants found, that leaves reaching full expansion more than doubled their net rate of carbon dioxide fixation. Studies on the physiology of CO2 effect aim at understanding mechanisms which control interactions of CO2 with other environmental factors, such as water or sun deficit [3,4,5,9].
Methyl alcohol may be an alternate carbon source for plants. According to Nonomura and Benson [10] methanol treated plants showed increased turgor, higher growth rates and consequently gave higher yield than the control plants. Only C3 plants, that is those which during photosynthetic carboxylation produce ribulose 1,5-diphosphate and then 3-phosphoglyceric acid respond to methanol by increased biomass production, since carbon dioxide resulting from rapid oxidation of methanol can successfully compete with oxygen for RuBisCO – [11]. Hemming et al. [7] who studied the rate of metabolism in pepper, petunia and tomato plant tissues found that brief exposure to aqueous methanol solutions increased the metabolic heat rate, which resulted in enhanced carbon conversion efficiency. Furthermore plants which grow in an CO2 enriched atmosphere are less susceptible to drought, since their stomata are closed, transpiration decreases, and net photosynthesis is thus elevated [2,14].
Considering the possibility of using methanol as a measure for yield increases, and saving irrigation water, greenhouse and field experiments were carried out to assess the impact of methanol solution on selected crops cultivated in moderate climate zone.
MATERIAL AND METHODS
Three-year field experiments were carried out on 0.5 m2 microplots in 4 replications. The first factor was overhead irrigation applied so as to maintain 70-80% field water capacity. The control plants grew under natural conditions. Methanol (second factor) was applied in aqueous solutions of 10, 20, 30 and 40%. Each solution, also the water applied to control plants contained 0.2% glycine and 0.4% Florovit (micro- and macrofertliser). Plants of high rate of photorespiration when treated with methanol yield two molecules of serine per entry of two molecules of glycine thus leading to twice the sucrose being produced. For this reason Nonomura and Benson [10] recommend addition of glycine to methanol spray. Methanol-treated plants show also increased demand for minerals, hence the use of Florovit (N - 3%, K - 2% and microelements - Cu, Fe, Mn, Mo, Zn, Ca, S).
Plants were treated with the methanol solutions 4-5 times over vegetation in one-week intervals, in June to July. The test crops were: ‘Betalux’ tomato, ‘Cezar F-1’ cucumber, ‘Igołomska’ bean, ‘Colibri’ sugar beet and ‘Lirajet’ winter rape. At the time of full vegetative development, photosynthetic activity - CO2 assimilation, transpiration, leaf conductance and CO2 concentration in substomatal cells were measured with a LC-4 gas analyser in situ. The activity of nitrate reductase was analysed in leaves, using reduced NADH as hydrogen donor, that of phosphatase by colorymetry.
The growth of winter rape seedlings was tested in a growth chamber. 15 seeds were planted in 8-cm styrofoam cups containing vermiculite, kept under constant conditions of light (126 µE · m-2 · s-1, 16h light, 8h dark), and temperature 22 ± 1°C). After emergence 30 ml of ½ strength Hoagland medium were applied to each cup. 20-old-day plants were treated with 0, 10, 20, 30, 40% methanol solution fortified with 0.2% glycine. Two days after treatment, 10 largest seedlings were selected from each cup for shoot length, fresh as well as dry matter determination. The plant yield was analysed with Tukey test, at p = 95%.
RESULTS AND DISCUSSION
Data presented in Tables 1-3 showed that supplemental irrigation and methanol treatment positively affected the plant photosynthesis. As a result of overhead irrigation, an increased CO2 assimilation and transpiration rates were statistically confirmed in leaves of all three tested plants, whereas such effect of methanol was found in tomato and sugar beet leaves, to a lesser extent in bean. As for sugar beet, the impact of methanol on carbon dioxide assimilation surpassed that of supplemental irrigation. According to Nonomura and Benson [10] methanol reduces the plant photorespiration, and the rapidly oxidized methanol leads to formaldehyde incursion with tetrahydrofolate. As a result, the doubling of serine content could lead to twice the sucrose being produced through the serine intermediate [13]. Abundant CO2 supply from methanol causes the redirection of photorespiration from catabolism to anabolism [8,12]. Data of Tab. 5 showed that young plants rapidly reacted to diluted methanol application. The leaves activity of nitrate reductase was by over 50% higher, and of alkaline phosphatase by 32%. These findings support the view of Nonomura and Benson [10] who reported that methanol was rapidly oxidized to CO2 and then incorporated into structural compounds. Furthermore, the increased sucrose production improved the plant turgidity, hence a lesser susceptibility of methanol – treated plants to water deficit.
Table 1. Photosynthetic activity of bean leaves |
Treatment |
A* |
T |
Ci |
Gs |
|
Water |
Methanol |
||||
Control |
Control |
10.51 |
2.14 |
305 |
0.15 |
Control |
30% |
11.22 |
2.98 |
290 |
0.13 |
Irrigation |
Control |
11.23 |
3.12 |
270 |
0.13 |
Irrigation |
30% |
12.34 |
3.46 |
274 |
0.14 |
LSD p=0.05 for: irrigation |
1.22 |
0.57 |
ns |
0.02 |
*A – µM CO2·m-2 · s-1, T – transpiration M · m-2 · s-1, Ci – CO2 concentration in stomatal chamber, Gs – stomatal conductance, ns – non-significant difference |
Table 2. Photosynthetic activity of sugar beet leaves |
Treatment |
A* |
T |
Ci |
Gs |
|
Water |
Methanol |
||||
Control |
Control |
8.3 |
3.20 |
364 |
0.66 |
Control |
30% |
12.3 |
4.13 |
362 |
0.06 |
Irrigation |
Control |
10.7 |
5.25 |
380 |
0.10 |
Irrigation |
30% |
15.4 |
5.74 |
377 |
0.12 |
LSD p=0.05 for: irrigation |
1.02 |
0.56 |
Ns |
0.02 |
* for explanations, see Table 1 |
Table 3. Photosynthetic activity of tomato leaves |
Treatment |
A* |
T |
Ci |
Gs |
|
Water |
Methanol |
||||
Control |
Control |
2.56 |
0.75 |
147 |
0.03 |
Control |
30% |
3.88 |
1.17 |
136 |
0.04 |
Irrigation |
Control |
6.86 |
2.16 |
188 |
0.10 |
Irrigation |
30% |
8.78 |
2.51 |
189 |
0.13 |
LSD p=0.05 for: irrigation |
0.523 |
0.082 |
13.3 |
0.006 |
* for explanations, see Table 1 |
Table 4. Growth of winter rape seedlings |
Methanol treatment |
Shoot length |
Fresh weight |
Dry weight |
|||
mm |
% |
g·plant -1 |
% |
g·plant -1 |
% |
|
Control |
298 |
100 |
13.9 |
100 |
1.90 |
100 |
10 |
379 |
127 |
23.1 |
166 |
2.98 |
157 |
20 |
401 |
134 |
26.1 |
187 |
3.46 |
182 |
30 |
392 |
131 |
25.4 |
182 |
3.48 |
183 |
40 |
328 |
110 |
17.5 |
125 |
2.55 |
134 |
LSD p=0.05 |
21.0 |
2.07 |
0.33 |
Table 5. Enzyme activities and biomass synthesis by spring rape seedling leaves, 20-day old plants |
Methanol |
Alkaline phosphatase |
Nitrate reductase |
Fresh matter |
Dry matter |
0 |
1.23 |
31.6 |
1.62 |
0.13 |
10 |
1.58 |
36.7 |
2.49 |
0.19 |
20 |
1.62 |
47.9 |
3.11 |
0.24 |
40 |
1.46 |
42.0 |
1.66 |
0.13 |
LSD p=0.05 |
0.079 |
4.75 |
0.629 |
0.049 |
Data presented in Tables 6, 7 and 8 have shown that yield increases caused by methanol solutions ranged from 12% for sugar beet, 20% for bean to 30% for tomato. Comparison of methanol effects on seedlings and mature plants indicates that the young seedlings reaction to this treatment was more pronounced than that of the resulting crop (Tab. 4 and 9). The yield of seeds given by rape plants treated with 30 or 40% methanol exceeded that of the control plants by 30%, whereas the dry matter of seedlings sprayed with 30% methanol was higher by over 80%. This discrepancy may indicate that maturing plants had a greater need for biomass supply. The plant products of photosynthesis are used for the development of seeds, but first of all for building of leaves, branches and fruit. This is also in concord with the elevated photosynthesis of methanol – treated leaves. Similar results were repor ted by Zbieć et al. [14].
Table 6. Bean seed yield, g · 0.5 m-2 |
Treatment |
|||||||||
Not irrigated |
Irrigated |
||||||||
Methanol treatment, % |
|||||||||
0 |
10 |
20 |
30 |
40 |
0 |
10 |
20 |
30 |
40 |
209 |
216 |
223 |
251 |
245 |
250 |
248 |
248 |
261 |
263 |
LSD p=0.05 for: irrigation 7.03 |
Table 7. Sugar beet yield, kg · 0.5 m-2 |
Methanol treatment, % |
Not irrigated |
Irrigated |
||
roots |
leaves |
roots |
leaves |
|
0 |
5.92 |
5.39 |
7.04 |
6.27 |
10 |
6.06 |
5.48 |
7.08 |
6.40 |
20 |
6.64 |
5.46 |
7.49 |
6.76 |
30 |
6.65 |
5.43 |
7.63 |
6.93 |
40 |
6.48 |
5.22 |
7.22 |
6.72 |
LSD p=0.05 for: irrigation |
0.45 |
0.61 |
Table 8. Tomato yield, kg · 0.5 m-2 |
Treatment |
|||||||||
Not irrigated |
Irrigated |
||||||||
Methanol treatment, % |
|||||||||
0 |
10 |
20 |
30 |
40 |
0 |
10 |
20 |
30 |
40 |
2.49 |
2.71 |
3.25 |
3.26 |
2.80 |
3.25 |
3.48 |
3.61 |
3.58 |
3.68 |
LSD p=0.05 for: irrigation 0.18 |
Table 9. Winter rape yield and yield components |
Methanol treatment |
Number of branches |
Number of siliques |
Seed yield |
|||
per plant |
% |
per plant |
% |
g·plant -1 |
% |
|
0 |
5.1 |
100 |
115 |
100 |
25.9 |
100 |
20 |
6.8 |
133 |
150 |
130 |
32.6 |
126 |
30 |
6.8 |
133 |
151 |
130 |
33.5 |
129 |
40 |
7.0 |
137 |
151 |
130 |
34.2 |
132 |
LSD p=0.05 |
0.39 |
6.54 |
3.47 |
Since the effects of supplemental irrigation were better than those of methanol application, it can be assumed that the beneficial impact of methanol is expressed to a greater extent in plants which are more susceptible to water deficit and grow better under hot weather conditions and well supplied with water. Information provided by some Israeli scientists who did experiments with methanol in greenhouses (personal information) supports the view that methanol application for yield increase can be successful in controlled environment conditions, since under hot climate and in the field, methanol rapidly evaporates, thus is ineffective.
CONCLUSIONS
Water solutions of methanol alcohol applied to plants of the C-3 carbon conversion cycle caused increase in carbon dioxide assimilation and biomass synthesis. Plants which had been treated with methanol solutions, particularly tomato and sugar beet showed an 50% increase in nitrate reductase activity, and significantly enhanced CO2 assimilation.
Bean, sugar beet, tomato, oil seed rape treated with 30% methanol solution yielded by 12 to 30% higher than the control plants.
The methanol treated plants were less susceptible to water deficit, in some cases their yield equalled that of the irrigated plants.
REFERENCES
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Irena Zbieć, Stanisław Karczmarczyk, Cezary Podsiadło
Department of Plant Production and Irrigation
Agricultural University of Szczecin
Słowackiego 17, 71-434 Szczecin, Poland
e-mail: skarczmarczyk@agro.ar.szczecin.pl
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