Electronic Journal of Polish Agricultural Universities (EJPAU) founded by all Polish Agriculture Universities presents original papers and review articles relevant to all aspects of agricultural sciences. It is target for persons working both in science and industry,regulatory agencies or teaching in agricultural sector. Covered by IFIS Publishing (Food Science and Technology Abstracts), ELSEVIER Science - Food Science and Technology Program, CAS USA (Chemical Abstracts), CABI Publishing UK and ALPSP (Association of Learned and Professional Society Publisher - full membership). Presented in the Master List of Thomson ISI.
2003
Volume 6
Issue 1
Topic:
Agronomy
ELECTRONIC
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Zbieć I. , Karczmarczyk S. , Podsiadło C. 2003. RESPONSE OF SOME CULTIVATED PLANTS TO METHANOL AS COMPARED TO SUPPLEMENTAL IRRIGATION, EJPAU 6(1), #01.
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

 

ABSTRACT

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
                          methanol
                            interaction

1.22
1.96
ns

0.57
ns
ns

ns
ns
ns

0.02
ns
ns

*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
                          methanol
                            interaction

1.02
1.66
1.95

0.56
0.61
ns

Ns
ns
ns

0.02
ns
ns

* 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
                          methanol
                            interaction

0.523
0.83
ns

0.082
0.30
ns

13.3
ns
ns

0.006
ns
ns

* 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
treatment
%

Alkaline phosphatase
µ·100 g-1

Nitrate reductase
µMNO2·g-1·h-1

Fresh matter
mg·m-2·h-1

Dry matter
mg·m-2·h-1

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
                          methanol       6.14
                        interaction     ns

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
                           methanol
                            interaction

0.45
0.56
ns

0.61
ns
ns

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
                         methanol       0.45
                         interaction      0.60

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

  1. 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.

  2. Bean, sugar beet, tomato, oil seed rape treated with 30% methanol solution yielded by 12 to 30% higher than the control plants.

  3. The methanol treated plants were less susceptible to water deficit, in some cases their yield equalled that of the irrigated plants.

REFERENCES

  1. Abdel-Latif A., Schmieden U., Barakat S, Wild A., 1996. Physiological and biochemical responses of sunflower plant to enhanced CO2 level. Plant Physiol. & Biochem., Spec. Issue, 133.

  2. Besford R.T., 1993. Photosynthetic acclimation in tomato plants grown in high CO2. CO2 and Biosphere, Kluwer Acad. Publ., Belgium, Vegetatio 104/105, 441-448.

  3. Camporredondo G., Dunabectia M., Gonzales-Moro B., Gonzales Murna C., 1996. Effect of the interruption of photorespiration on CO2 assimilation under different light intensities in Maize (C-4) and barley (C-3). Plant Physiol. & Biochem., Spec. Issue, 126.

  4. Dahlman R.C., 1993. CO2 and plants revisited. CO2 and Biosphere, Kluwer Acad. Publ., Belgium, Vegetatio 104/105, 339-355.

  5. Devlin R.M., Bhowmik P.C., Karczmarczyk S.J., 1994. Influence of methanol on plant growth. Plant Growth Regul., Soc. Amer. Quart. 22 (4), 102-108.

  6. Fisher B.U., Nosberger J., Frehner M., 1996. Effect of an elevated partial pressure of CO2 on source – sink relations during regrowth of Lollium perenne L. Plant Physiol. & Biochem., Spec. Issue, 121.

  7. Grimmer C., Konor E., 1996. Effects of elevated CO2 on carbohydrate metabolism and growth of Ricinus comm. Plant Physiol. & Biochem., Spec. Issue, 123.

  8. Hemming D.J.B., Criddle R.S., Hansen L.D., 1995. Effects of methanol on plant respiration. J. Plant Physiol. 146, 193-198.

  9. Karczmarczyk S.J., Devlin R. M., Zbieć I.I., 1995. Influence of methanol on winter rape seedlings. Acta Agrobotanica 48 (2), 37-42.

  10. Nonomura A.M., Benson A.A., 1992. The path of carbon in photosynthesis: Methanol and light. Research in photosynthesis 3 (18), 911-914.

  11. Nonomura A.M., Benson A.A., 1993. Agrimethanol a foliar nutrient. Proc. 20th Ann. Meeting. Plant Growth Soc. Amer., 1-7.

  12. Ogren W.L., Bowes G., 1971. Ribulose diphosphate carboxylase regulates soybean photorespiration. Nature New Biol. 230, 159-160.

  13. Rowe R.N., Farr D. J., Richards B.A.J., 1994. Effects of foliar and root applications of methanol or ethanol on the growth of tomato plants (Lycopersicon esculentum Mill.). New Zealand J. Crop & Hort. Sci. 22, 335-337.

  14. Zbieć I.I., Karczmarczyk S., Koszański Z., 1999. Influence of methanol on some cultivated plants. Folia Univ. Agric. Stetin., Agricultura 73, 217-220.


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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