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Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

Effect of Open Field and Open Shade Conditions on the Growth
and Phytochemical Constituents of Amaranthus cruentus
Omobolanle Elizabeth ADE-ADEMILUA*, Moses EYEMI
Department of Botany, Faculty of Science, University of Lagos, Akoka-Yaba, Lagos, Nigeria.
*Email: oade-ademilua@unilag.edu.ng; toeademilua@yahoo.com.
Abstract
The growth and phytochemical constituents of Amaranthus cruentus plants under open shade and open field
conditions were studied. Plants grown under open field had significantly higher plant height, number of leaves,
fresh weight, dry weight and leaf area throughout the period of the analysis than those grown under open shade.
Plants grown under open field condition had significantly higher (p = 0.05) amount of total flavonoids and total
tannin and total antioxidant capacity. Nevertheless, the total phenol was significantly higher in plants grown
under open shade condition. Leaf extracts of plants grown under open field condition also had significantly
higher DPPH scavenging activity based on the IC50 value (38.31 µg/ml) than those of plants grown under open
shade (52.35 µg/ml). The results of this study show that Amaranthus cruentus plants should be grown under
open field to obtain better vegetative growth as well as higher phytochemical and antioxidant capabilities.
KEY WORDS: Amaranthus cruentus, open field, open shade, growth, antioxidant
1. Introduction
The value of light cannot be over-emphasized because it is a vital factor that enhance or limit plant growth
(López et al. 2004). However, the intensity of light on plant in addition to the photosynthetic activities
determines the extent to which phytochemicals can be produced (Nasrullahzadeh et al. 2007). Shade imposes a
limitation to biological productivity in plants although the extent of the limitation varies with the shade tolerance
of the species and the nitrogen supply (Wong 1991).
The value of medicinal plants lies in some chemical substances that produce a definite physiological action on
the human body (Edeoga et al. 2005). Vegetables are indispensable constituents of human diets. They supply
the body with minerals, vitamins and certain hormone precursors in addition to proteins and energy. Recent
reports have pointed to the fact that Amaranthus species have a high concentration of antioxidant components
(Cao et al. 1996; Gill et al. 1999; Hunter & Fletcher 2002). Amaranthus cruentus commonly known as mexican
grain amaranth, red amaranth and purple amaranth is a tropical leaf vegetable grown in most tropical regions of
the world for its vegetable protein (Adeniji et al. 2006).
There is limited research to determine what impact air temperature and sunlight intensity has on the production
of biomass and secondary plant compounds (Khandaker et al. 2009). Khandaker et al. (2009) reported that A.
tricolor grew better and had higher betacyanin when grown under high air temperature and sunlight. The better
yield was associated more to higher air temperature than sunlight. Khandaker et al. (2009) report suggests that
it is likely that all Amaranthus species will grow better under open field condition, however we sought to
investigate not only this hypothesis in A. crentus but also if phytochemicals such as flavonoid and phenols and
the antioxidant capacity of the amaranth is affected by high air temperature and sunlight under open field
conditions.
2. Materials and Methods
The seeds of Amaranthus cruentus were collected from Nigeria Horticultural Research Institute (NIHORT),
Ibadan. The experiment was set up at the Botanical Garden of the University of Lagos. Seeds were germinated
in the nursery and seedlings were transplanted into planting bags filled with loamy soil, fourteen days after
sowing. The planting bags were divided into two: a set was placed under open field and another set was placed
under open shade (under a Plumera alba tree), all under canopies made up of wire gauze nets and a transparent
polythene sheet roof.

33
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

2.1 Measurement of growth parameters
The plants height, number of leaves, total leaf area, fresh weights and dry weights were determined at 14 days
interval from 14 days after transplanting. The plant height was measured from the base (i.e. the point at which
the stem is in contact with the soil) to the apex using a centimeter ruler. The fresh weight of the replicates of the
plants was determined using an electronic balance (Mettler Toledo Model AB 204) after the soil in the roots had
been carefully rinsed off. Total leaf area per plant was determined by calculating the area of traced leaf outlines
on a graph paper. Plants were then oven dried at 80°C for three days and the dry weight was determined.
2.2 Determination of the phytochemical properties
Freshly cut leaves were collected 56 days after transplanting, air-dried and grind into powder using a grinding
machine. 100g of each powdered sample was weighed and soaked in 300 mls of methanol (80 %) for 48 hours.
Thereafter, the extracts were filtered using Whatmann filter paper. This process was repeated twice for complete
extraction. The filtrate was concentrated below 40 ºC using a Rotary evaporator (Buchi Rotavapor R-215) and
reduced extracts were transferred into evaporating dish and air-dried. Extracts were weighed and percentage
yield was calculated. The extracts were then used to determine the following total flavonoid (Nile & Khobragade
2010), total phenol (Khanahmadi et al. 2010), total antioxidant capacity (Nile & Khobragade 2010) and 1diphenyl-2-picrylhydrazil (DPPH) free radical scavenging activity (Adesegun et al. 2008). The IC50 value which
is the concentration (in µg/ml) of extracts that scavenges the DPPH radicals by 50% was determined (Prashanth
et al. 2010).
2.3 Statistical analysis
Statistical analysis was carried out in triplicate per analysis on samples from both open field and open shade
populations. A single factor analysis of variance (ANOVA was used to analyze the treatments at less than 5%
level of significance (Zar 1984).
3. Results and Discussion
The air temperature and light intensity of the open field site used in this study was about 1.8 °C and 26.7 to
44.2 % higher than that of the open shade respectively.
3.1 Biomass Yield
The heights of plants grown under open field was significantly higher (p = 0.05) than that of plants grown under
shade except at 28 days of treatment when that of the plants grown under shade was significantly higher (p =
0.05), as shown in Figure 1. The fresh and dry weight of plants grown in the open field condition were
significantly higher (p = 0.05) than that of plants grown under open shade condition throughout the period of
analysis (Figure 2 and 3 respectively). The number of leaves of plants under open field were significantly higher
(at p = 0.05) than that of plants grown under open shade from 42 days of treatment (Figure 4). The total leaf
area of plants grown under open field was significantly higher (p = 0.05) than those grown under open shade
from 28 days of treatment (Figure 5).
The results are not surprising as it is similar to reports on other Amaranthus species such as A. tricolor
(Khandaker et al. 2009) and A. hypochondriacus (López et al. 2004).

34
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

Figure 1: Mean height of Amaranthus cruentus plants grown under open
field and open shade conditions. Plotted means against number of days
of treatment represented with different letters shows significant
difference

Figure 2: Mean fresh weight of Amaranthus cruentus plants grown under open
field and open shade conditions. Plotted means against number of days of
treatment represented with different letters shows significant difference

35
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

Figure 3: Mean dry weight of Amaranthus cruentus plants grown under open field
and open shade conditions. Plotted means against number of days of treatment
represented with different letters shows significant difference

Figure 4: Mean number of leaves of Amaranthus cruentus plants grown under open
field and open shade conditions. Plotted means against number of days of treatment
represented with different letters shows significant difference

36
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

Figure 5: Mean total leaf area of Amaranthus cruentus plants grown under open field and open shade. Plotted
means against number of days of treatment represented with different letters shows significant difference
3.2 Phytochemical content
Table 1: Phytochemical constituents of leaves of Amaranthus cruentus plants
grown under open field and open shade condition.
Test

Open field

Open shade

Total flavonoids (mg/g re)

11.58a

10.12b

Total phenol (mg/g gae)

2.99b

4.32a

Total tannin (mg/g tae)

8.77a

6.39b

Total antioxidant capacity (mg/g aae)

12.12a

6.49b

RE = Rutin Equivalent; GAE = Gallic Acid Equivalent;
TAE = Tannin Acid Equivalent; AAE = Ascorbic Acid Equivalent
Leaf extracts of plants grown under open field conditions had significantly higher (p = 0.05) total flavonoids,
total tannins and total antioxidant capacity than those of plants grown under open shade conditions (Table 1).
However, leaves of plants grown under open shade had a significantly higher (p = 0.05) total phenol content than
that of plants grown under open field conditions.
3.3 DPPH scavenging activity
Table 2 shows the percentage DPPH radical scavenged by leaf extracts of plants grown under open field and
open shade conditions.

37
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

Table 2: Percentage DPPH radical scavenging activity of leaves of Amaranthus
cruentus plants grown under open field and open shade condition
Concentration (µg/ml)
25
50

56.44

75

65.33
94.67

25

39.27

50

49.73

75

61.53

100

Open
shade

44.88

100

Open field

% DPPH radical scavenged

IC50 (µg/ml)

93.12

38.31

57.35

The IC50 value of the leaf extracts of plants grown under open field was significantly higher (38.31 µg/ml) than
those of plants grown under open shade (52.35 µg/ml). This shows that the leaves of plants grown under open
field have a significantly higher DPPH scavenging activity than those grown under open field conditions. A
higher DPPH scavenging activity signifies a higher antioxidant capacity (Prashanth et al. 2010).
4. Conclusion
The combination of the various antioxidant compounds like tannins, phenols and flavonoid contributes to high
antioxidant capacity. This result of this study shows that Amaranthus cruentus requires open field conditions not
only for better vegetative growth but also for higher medicinal value.
References
Adeniji A.O., Dairo F.A. & Fasuyi A.O. (2006), “Tropical vegetable (Amaranthus cruentus) leaf meal as
alternative protein supplement in broiler starter diets: Bionutritional evaluation”. Journal of Central European
Agriculture 9, 23-34.
Adesegun S.A., Coker H.A. & Elechi N.A. (2008), “Antioxidant activities of methanolic extract of Sapium
elliticum”. Pakistan. Journal of Biological Science 11, 453- 457.
Cao G., Sofic E. & Prior R.L. (1996), “Antioxidant capacity of tea and common vegetables”, Journal of
Agriculture and Food Chemistry 44: 3426–3431.
Edeoga H.O., Okwu D.E. & Mbaebie B. (2005), “Phytochemical constituents of some Nigerian medicinal
plants”, African Journal of Biotechnology 4, 685-688.
Gill M.I., Ferreres F. & Thomas-Barberan F.A. (1999), “Effect of postharvest storage and processing on the
antioxidant constituents (flavonoids and vitamin C) of fresh-cut spinach”, Journal of Agriculture and Food
Chemistry 47, 2213–2217.
Hunter K.J. & Fletcher J.M. (2002), “The antioxidant activity and composition of fresh, frozen, jarred and
canned vegetables”, Innovative Food Science and Emerging Technologies 3, 399 – 406.

38
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.3, No.12, 2013

www.iiste.org

Khanahmadi M., Rezazadeh S.H. & Taran M. (2010), “In vitro antimicrobial and antioxidant properties of
Smyrnium cordifolium BIOSS (Umbeliferae) extract”, Asian Journal of Plant Science 9, 99-103.
Khandaker L, Akond A.S.M. & Oba S. (2009), “Air temperature and sunlight intensity of different growing
period affects the biomass, leaf color and betacyanin pigment accumulations in red amaranth (Amaranthus
tricolor L.)”, Journal of Central European Agriculture 10, 439 – 448.
López Y.N., Alejandro B.L., Délano-Frier J. & Barrios E.P. (2004), “Light Intensity and activity of trypsin
inhibitors in Amaranth leaves and seeds”, Revista Fitotecnia Mexicana 27: 127-132.
Nasrullahzadeh S., Ghassemi-Golezani K.., Javanshir A., Valizade M. & Shakiba M.R. (2007), Effects of shade
stress on ground cover and grain yield of faba bean. Journal of Food Agriculture and Environment 5: 337-340.
Nile S.H. & Khobragade C.N. (2010), “Antioxidant activity and flavonoid derivatives of Plumbago zeylanica”,
Journal of Natural Products 3, 130-133.
Prashanth S., Kumarb A.A., Madhub B. & Kumara Y.P. (2010), “Antihyperglycemic and antioxidant activity of
ethanolic extract of Madhuca longifolia bark”, International Journal of Pharmaceutical Sciences Review and
Research 5, 89 – 94.
Wong G. (1991), “Shade tolerance of tropical forages: A review”, In: Shelton HM and Stuart WW (eds) Forages
for Plantation Crops. ACIAR, Canberra, pp 64-69.
Zar, J.H. (1984), “Biostatistical Analysis”. Prentice-Hall Inc., New Jersey, USA.

39
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  • 1. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org Effect of Open Field and Open Shade Conditions on the Growth and Phytochemical Constituents of Amaranthus cruentus Omobolanle Elizabeth ADE-ADEMILUA*, Moses EYEMI Department of Botany, Faculty of Science, University of Lagos, Akoka-Yaba, Lagos, Nigeria. *Email: oade-ademilua@unilag.edu.ng; toeademilua@yahoo.com. Abstract The growth and phytochemical constituents of Amaranthus cruentus plants under open shade and open field conditions were studied. Plants grown under open field had significantly higher plant height, number of leaves, fresh weight, dry weight and leaf area throughout the period of the analysis than those grown under open shade. Plants grown under open field condition had significantly higher (p = 0.05) amount of total flavonoids and total tannin and total antioxidant capacity. Nevertheless, the total phenol was significantly higher in plants grown under open shade condition. Leaf extracts of plants grown under open field condition also had significantly higher DPPH scavenging activity based on the IC50 value (38.31 µg/ml) than those of plants grown under open shade (52.35 µg/ml). The results of this study show that Amaranthus cruentus plants should be grown under open field to obtain better vegetative growth as well as higher phytochemical and antioxidant capabilities. KEY WORDS: Amaranthus cruentus, open field, open shade, growth, antioxidant 1. Introduction The value of light cannot be over-emphasized because it is a vital factor that enhance or limit plant growth (López et al. 2004). However, the intensity of light on plant in addition to the photosynthetic activities determines the extent to which phytochemicals can be produced (Nasrullahzadeh et al. 2007). Shade imposes a limitation to biological productivity in plants although the extent of the limitation varies with the shade tolerance of the species and the nitrogen supply (Wong 1991). The value of medicinal plants lies in some chemical substances that produce a definite physiological action on the human body (Edeoga et al. 2005). Vegetables are indispensable constituents of human diets. They supply the body with minerals, vitamins and certain hormone precursors in addition to proteins and energy. Recent reports have pointed to the fact that Amaranthus species have a high concentration of antioxidant components (Cao et al. 1996; Gill et al. 1999; Hunter & Fletcher 2002). Amaranthus cruentus commonly known as mexican grain amaranth, red amaranth and purple amaranth is a tropical leaf vegetable grown in most tropical regions of the world for its vegetable protein (Adeniji et al. 2006). There is limited research to determine what impact air temperature and sunlight intensity has on the production of biomass and secondary plant compounds (Khandaker et al. 2009). Khandaker et al. (2009) reported that A. tricolor grew better and had higher betacyanin when grown under high air temperature and sunlight. The better yield was associated more to higher air temperature than sunlight. Khandaker et al. (2009) report suggests that it is likely that all Amaranthus species will grow better under open field condition, however we sought to investigate not only this hypothesis in A. crentus but also if phytochemicals such as flavonoid and phenols and the antioxidant capacity of the amaranth is affected by high air temperature and sunlight under open field conditions. 2. Materials and Methods The seeds of Amaranthus cruentus were collected from Nigeria Horticultural Research Institute (NIHORT), Ibadan. The experiment was set up at the Botanical Garden of the University of Lagos. Seeds were germinated in the nursery and seedlings were transplanted into planting bags filled with loamy soil, fourteen days after sowing. The planting bags were divided into two: a set was placed under open field and another set was placed under open shade (under a Plumera alba tree), all under canopies made up of wire gauze nets and a transparent polythene sheet roof. 33
  • 2. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org 2.1 Measurement of growth parameters The plants height, number of leaves, total leaf area, fresh weights and dry weights were determined at 14 days interval from 14 days after transplanting. The plant height was measured from the base (i.e. the point at which the stem is in contact with the soil) to the apex using a centimeter ruler. The fresh weight of the replicates of the plants was determined using an electronic balance (Mettler Toledo Model AB 204) after the soil in the roots had been carefully rinsed off. Total leaf area per plant was determined by calculating the area of traced leaf outlines on a graph paper. Plants were then oven dried at 80°C for three days and the dry weight was determined. 2.2 Determination of the phytochemical properties Freshly cut leaves were collected 56 days after transplanting, air-dried and grind into powder using a grinding machine. 100g of each powdered sample was weighed and soaked in 300 mls of methanol (80 %) for 48 hours. Thereafter, the extracts were filtered using Whatmann filter paper. This process was repeated twice for complete extraction. The filtrate was concentrated below 40 ºC using a Rotary evaporator (Buchi Rotavapor R-215) and reduced extracts were transferred into evaporating dish and air-dried. Extracts were weighed and percentage yield was calculated. The extracts were then used to determine the following total flavonoid (Nile & Khobragade 2010), total phenol (Khanahmadi et al. 2010), total antioxidant capacity (Nile & Khobragade 2010) and 1diphenyl-2-picrylhydrazil (DPPH) free radical scavenging activity (Adesegun et al. 2008). The IC50 value which is the concentration (in µg/ml) of extracts that scavenges the DPPH radicals by 50% was determined (Prashanth et al. 2010). 2.3 Statistical analysis Statistical analysis was carried out in triplicate per analysis on samples from both open field and open shade populations. A single factor analysis of variance (ANOVA was used to analyze the treatments at less than 5% level of significance (Zar 1984). 3. Results and Discussion The air temperature and light intensity of the open field site used in this study was about 1.8 °C and 26.7 to 44.2 % higher than that of the open shade respectively. 3.1 Biomass Yield The heights of plants grown under open field was significantly higher (p = 0.05) than that of plants grown under shade except at 28 days of treatment when that of the plants grown under shade was significantly higher (p = 0.05), as shown in Figure 1. The fresh and dry weight of plants grown in the open field condition were significantly higher (p = 0.05) than that of plants grown under open shade condition throughout the period of analysis (Figure 2 and 3 respectively). The number of leaves of plants under open field were significantly higher (at p = 0.05) than that of plants grown under open shade from 42 days of treatment (Figure 4). The total leaf area of plants grown under open field was significantly higher (p = 0.05) than those grown under open shade from 28 days of treatment (Figure 5). The results are not surprising as it is similar to reports on other Amaranthus species such as A. tricolor (Khandaker et al. 2009) and A. hypochondriacus (López et al. 2004). 34
  • 3. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org Figure 1: Mean height of Amaranthus cruentus plants grown under open field and open shade conditions. Plotted means against number of days of treatment represented with different letters shows significant difference Figure 2: Mean fresh weight of Amaranthus cruentus plants grown under open field and open shade conditions. Plotted means against number of days of treatment represented with different letters shows significant difference 35
  • 4. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org Figure 3: Mean dry weight of Amaranthus cruentus plants grown under open field and open shade conditions. Plotted means against number of days of treatment represented with different letters shows significant difference Figure 4: Mean number of leaves of Amaranthus cruentus plants grown under open field and open shade conditions. Plotted means against number of days of treatment represented with different letters shows significant difference 36
  • 5. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org Figure 5: Mean total leaf area of Amaranthus cruentus plants grown under open field and open shade. Plotted means against number of days of treatment represented with different letters shows significant difference 3.2 Phytochemical content Table 1: Phytochemical constituents of leaves of Amaranthus cruentus plants grown under open field and open shade condition. Test Open field Open shade Total flavonoids (mg/g re) 11.58a 10.12b Total phenol (mg/g gae) 2.99b 4.32a Total tannin (mg/g tae) 8.77a 6.39b Total antioxidant capacity (mg/g aae) 12.12a 6.49b RE = Rutin Equivalent; GAE = Gallic Acid Equivalent; TAE = Tannin Acid Equivalent; AAE = Ascorbic Acid Equivalent Leaf extracts of plants grown under open field conditions had significantly higher (p = 0.05) total flavonoids, total tannins and total antioxidant capacity than those of plants grown under open shade conditions (Table 1). However, leaves of plants grown under open shade had a significantly higher (p = 0.05) total phenol content than that of plants grown under open field conditions. 3.3 DPPH scavenging activity Table 2 shows the percentage DPPH radical scavenged by leaf extracts of plants grown under open field and open shade conditions. 37
  • 6. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org Table 2: Percentage DPPH radical scavenging activity of leaves of Amaranthus cruentus plants grown under open field and open shade condition Concentration (µg/ml) 25 50 56.44 75 65.33 94.67 25 39.27 50 49.73 75 61.53 100 Open shade 44.88 100 Open field % DPPH radical scavenged IC50 (µg/ml) 93.12 38.31 57.35 The IC50 value of the leaf extracts of plants grown under open field was significantly higher (38.31 µg/ml) than those of plants grown under open shade (52.35 µg/ml). This shows that the leaves of plants grown under open field have a significantly higher DPPH scavenging activity than those grown under open field conditions. A higher DPPH scavenging activity signifies a higher antioxidant capacity (Prashanth et al. 2010). 4. Conclusion The combination of the various antioxidant compounds like tannins, phenols and flavonoid contributes to high antioxidant capacity. This result of this study shows that Amaranthus cruentus requires open field conditions not only for better vegetative growth but also for higher medicinal value. References Adeniji A.O., Dairo F.A. & Fasuyi A.O. (2006), “Tropical vegetable (Amaranthus cruentus) leaf meal as alternative protein supplement in broiler starter diets: Bionutritional evaluation”. Journal of Central European Agriculture 9, 23-34. Adesegun S.A., Coker H.A. & Elechi N.A. (2008), “Antioxidant activities of methanolic extract of Sapium elliticum”. Pakistan. Journal of Biological Science 11, 453- 457. Cao G., Sofic E. & Prior R.L. (1996), “Antioxidant capacity of tea and common vegetables”, Journal of Agriculture and Food Chemistry 44: 3426–3431. Edeoga H.O., Okwu D.E. & Mbaebie B. (2005), “Phytochemical constituents of some Nigerian medicinal plants”, African Journal of Biotechnology 4, 685-688. Gill M.I., Ferreres F. & Thomas-Barberan F.A. (1999), “Effect of postharvest storage and processing on the antioxidant constituents (flavonoids and vitamin C) of fresh-cut spinach”, Journal of Agriculture and Food Chemistry 47, 2213–2217. Hunter K.J. & Fletcher J.M. (2002), “The antioxidant activity and composition of fresh, frozen, jarred and canned vegetables”, Innovative Food Science and Emerging Technologies 3, 399 – 406. 38
  • 7. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.3, No.12, 2013 www.iiste.org Khanahmadi M., Rezazadeh S.H. & Taran M. (2010), “In vitro antimicrobial and antioxidant properties of Smyrnium cordifolium BIOSS (Umbeliferae) extract”, Asian Journal of Plant Science 9, 99-103. Khandaker L, Akond A.S.M. & Oba S. (2009), “Air temperature and sunlight intensity of different growing period affects the biomass, leaf color and betacyanin pigment accumulations in red amaranth (Amaranthus tricolor L.)”, Journal of Central European Agriculture 10, 439 – 448. López Y.N., Alejandro B.L., Délano-Frier J. & Barrios E.P. (2004), “Light Intensity and activity of trypsin inhibitors in Amaranth leaves and seeds”, Revista Fitotecnia Mexicana 27: 127-132. Nasrullahzadeh S., Ghassemi-Golezani K.., Javanshir A., Valizade M. & Shakiba M.R. (2007), Effects of shade stress on ground cover and grain yield of faba bean. Journal of Food Agriculture and Environment 5: 337-340. Nile S.H. & Khobragade C.N. (2010), “Antioxidant activity and flavonoid derivatives of Plumbago zeylanica”, Journal of Natural Products 3, 130-133. Prashanth S., Kumarb A.A., Madhub B. & Kumara Y.P. (2010), “Antihyperglycemic and antioxidant activity of ethanolic extract of Madhuca longifolia bark”, International Journal of Pharmaceutical Sciences Review and Research 5, 89 – 94. Wong G. (1991), “Shade tolerance of tropical forages: A review”, In: Shelton HM and Stuart WW (eds) Forages for Plantation Crops. ACIAR, Canberra, pp 64-69. Zar, J.H. (1984), “Biostatistical Analysis”. Prentice-Hall Inc., New Jersey, USA. 39
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