page 129

Effect of NPK and Zn on growth, flowering and bulb production in tulip under
polyhouse conditions in Kashmir

F. U. Khan, A. Q. Jhon, F. A. Khan1 and M. M. Mir
Division of Floriculture, Medicinal and Aromatic Plants

S.K. University of Agricultural Sciences and Technology of Kashmir, Shalimar Campus
Srinagar-191121 (J&K), India

E-mail: fukhanskuastk@rediffmail.com

ABSTRACT

Healthy and uniform bulbs of tulip cv. ‘Apeldoorn’ were planted in two consecutive growing seasons under
polyhouse conditions in FRBD design  to study the effect of nutrient management on growth, flowering and
bulb production in tulip in the Kashmir valley. Experimental treatments comprised of three levels of nitrogen
(0,75 and 150 kg ha-1) and two levels of phosphorus (0 and 50 kg ha-1), potassium (0 and 50 kg / ha) and zinc
(0 and 5 kg ha-1). Except for bulb survival, nitrogen @ 75 kg ha-1 significantly improved all the parameters.
However, further increase in dose of nitrogen (150 kg ha-1) influenced only a few parameters like scape length,
wrapper leaf area, vase life and bulblet weight per plant. Application of phosphorus, potassium and zinc also
resulted in better growth, flower quality and bulb production. Application of different nutrients caused increased
concentration of nutrients in leaf tissue, which resulted in better performance of the plant. Combined application
of N, P, K and Zn @ 75, 50, 50 and 5 kg ha-1, respectively, was found to be the most suitable dose for obtaining
better growth, quality flower and bulb production.

Key words: Tulip, nutrition, flowering, bulb production, polyhouse

INTRODUCTION

Tulip (Tulipa spp.) is known throughout the
temperate world and is considered an aristocrat of the pot,
garden, a field or forest. It is the leading ornamental bulbous
plant in the world and has gained popularity due to its beauty
and economic value. Tulips are excellent for cut flower,
garden display and pot culture. It is the top most flowering
geophyte of the Netherlands and occupies the fourth
position among the top ten cut flowers in the global
floriculture trade. The largest area under any true bulb crop
in the world is that of Tulipa, followed  by  Narcissus,  Iris,
Hyacinthus   and   Lilium    (Rees, 1972).  In  India,  tulips
are grown chiefly in the state of Jammu and Kashmir.
However,  there is  great  scope of growing tulips for various
purposes in temperate zones like Himachal Pradesh,
Uttranchal and other, similar hilly regions of the country.
Efforts on promoting commercial floriculture in our country
have started and protected cultivation of cut flowers opens
up newer avenues for quality production and export to earn
valuable foreign exchange. Due to its high aesthetic appeal,
tulips are in great demand, especially during Christmas,
Valentine’s Day, Mother’s Day and other festive occasions.

‘Apeldoorn’ is one of the most suitable cultivars of tulip
for cut flower production under polyhouse (Jhon and Khan,
2003). However, different aspects of production technology
need to be developed for getting higher quality/yield of
flower as well as bulb to fetch attractive returns. Work on
different aspects of production technologies, viz., planting
time (Jhon et al, 2004), growth environment (Jhon et al,
2005a) and suitable media (Jhon et al, 2005b) has been
conducted. Nutrients play an important role in growth and
development of any plant. However, information on this
aspect in tulip is scanty. Therefore, the present investigation
was carried out to study the effect of nutrients on growth,
flower quality and bulb production in tulip cv. ‘Apeldoorn’
under polyhouse conditions.

MATERIAL AND METHODS
The experiment was conducted at the Division of

Floriculture, Medicinal and Aromatic Plants, SKUAST (K),
Shalimar (located at an altitude of 1585 m amsl) during
two consecutive years, 2002 to 2004, under polyhouse
conditions. A polyhouse with steel pipe framework clad
with twin layer UV stabilized plastic sheet of 200 µm was
used to create modified environment. 10 cm dead space

J. Hort. Sci.
Vol. 1 (2): 129-134, 2006

1Plant Physiology Section, Division of Post Harvest Technology



page 130

J. Hort. Sci.
Vol. 1 (2): 129-134, 2006

Khan et al

130

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page 131

was ensured between plastic layers. The polyhouse was
additionally fitted with two high-pressure exhaust fans each
on the east and west, whereas four ventilators each were
provided on the north and south. Experimental treatments
comprised three levels of nitrogen (0, 75 and 150 kg ha-1)
and two levels each of phosphorus (0 and 50 kg ha-1),
potassium (0 and 50 kg ha-1) and zinc (0 and 5 kg ha-1).
Healthy and uniform bulbs of tulip cv. ‘Apeldoorn’ with 10
to 12 cm circumference were planted in beds of 0.54 m2

size each year on 30th October as per the factorial RBD
concept. There were two replications and eight
representative plants constituted one replication unit.
Growth media containing soil + Dal weed + sand in the
ratio of 2:1:1 at pH 6.8 was used for growing the plants.
Uniform cultural practices were followed throughout the
experimentation. Observations were recorded on bulb
survival (effective sprouting), stem thickness, wrapper leaf
(lower most leaf) area, days to flower (days after planting),
scape length, tepal diameter, vase life, bulb number and
weight of bulblets per plant. Leaf N, P and K analysis was
done as per the method of Jackson (1973). Data were
statistically analyzed as per procedure given by Panse and
Sukhatme (1978).

RESULTS AND DISCUSSION

Different nutrients and their levels had significant
effect on all the parameters studied (Table 1). Bulb survival
was not affected by any individual treatment of nutrients
during the first year (2002-03) of experimentation.
However, it was found to be significantly influenced by
increased doses of nitrogen and phosphorus during the
second year (2003-04) of experimentation. The reason for
the non-significant effect of nutrients on bulb survival may
be absence of adequate root system at the initial stage of
growth to absorb applied nutrients from soil. Non-
significant effect of nutrient application on bulb survival
has earlier been reported by Kumar and Singh (1998) in
tuberose.

Stem thickness was found to be significantly
influenced by addition of different levels of nitrogen,
phosphorus, potassium and zinc in both the years. Similarly,
wrapper leaf area also differed markedly with these nutrient
treatments, except with zinc during the first year of
experiment. Similar results on vegetative growth with
nitrogen have also been reported by Rani et al (2005) in
Lilium. Increased plant growth with nitrogen application

Table 2.  Interaction effect of various nutrients on growth, flower quality and bulb production in tulip

Treatment           Wrapper leaf area       Days to flowering        Scape length                Vase life              No. of bulbs/plant              Bulblet
(kg ha-1)                        (cm2)                          (DAP)                        (cm)                        (days)                                                  weight/plant (g)

2002-03 2003-04 2002-03 2003-04 2002-03 2003-04 2002-03 2003-04 2002-03 2003-04 2002-03 2003-04

N
0
 P

0
 K

0
 Z

0
123.26 129.36 126.83 123.38 34.63 31.64 6.08 6.12 0.88 1.00 3.80 4.25

N
0
 P

0
 K

0
 Z

5
121.27 130.50 124.08 121.50 35.00 34.23 6.17 6.25 0.82 1.00 3.75 4.20

N
0
 P

0
 K

50
 Z

0
127.46 131.15 123.00 120.50 37.50 34.68 6.83 6.75 0.76 0.95 4.37 4.45

N
0
 P

0
 K

50
 Z

5
126.95 132.58 125.58 122.00 36.50 33.22 6.83 6.62 0.76 0.92 4.62 6.30

N
0
 P

50
 K

0
 Z

0
128.85 130.35 124.00 121.25 33.88 30.66 6.58 6.50 0.88 1.00 4.62 4.75

N
0
 P

50
 K

0
 Z

5
128.18 131.56 125.50 122.25 36.63 36.45 6.08 6.12 1.08 1.17 6.37 6.55

N
0
 P

50
 K

50
 Z

0
126.85 133.50 124.58 119.50 35.75 35.75 7.08 7.12 0.88 1.05 5.87 6.01

N
0
 P

50
 K

50
 Z

5
123.76 134.00 123.58 118.00 38.50 37.46 7.33 7.25 1.01 1.18 6.50 6.60

N
75

 P
0
 K

0
 Z

0
130.24 135.00 134.17 120.50 35.00 36.21 6.58 7.12 0.88 1.00 6.37 6.50

N
75

 P
0
 K

0
 Z

5
132.11 137.20 130.00 126.50 36.25 35.83 6.67 6.75 0.94 1.11 6.37 6.52

N
75

 P
0
 K

50
 Z

0
136.48 136.30 124.17 121.75 37.50 37.11 6.83 6.50 0.94 1.11 6.25 6.45

N
75

 P
0
 K

50
 Z

5
131.17 142.15 126.08 124.50 37.50 37.96 6.92 7.00 0.94 1.09 6.62 6.75

N
75

 P
50

 K
0
 Z

0
137.20 141.65 131.83 128.00 38.50 39.46 6.75 7.25 1.07 1.28 7.12 7.25

N
75

 P
50

 K
0
 Z

5
141.59 143.95 129.75 125.25 39.25 42.35 6.75 7.25 1.07 1.25 7.87 7.78

N
75

 P
50

 K
50

 Z
0

136.98 143.50 121.42 120.50 40.00 41.69 7.92 8.00 1.13 1.31 7.37 7.48
N

75
 P

50
 K

50
 Z

5
139.83 146.35 121.00 119.50 44.25 43.48 8.17 8.25 1.19 1.37 8.12 7.75

N
150 

P
0
 K

0
 Z

0
130.40 131.95 132.50 129.00 37.00 39.23 6.00 7.50 0.94 1.10 7.12 7.05

N
150

 P
0
 K

0
 Z

5
127.46 135.80 128.00 125.25 36.63 37.14 6.25 6.25 0.88 1.06 6.87 7.25

N
150

 P
0
 K

50
 Z

0
135.65 141.25 126.25 125.00 37.50 38.50 6.92 6.50 0.88 1.05 5.62 7.20

N
150

 P
0
 K

50
 Z

5
134.84 142.36 125.50 122.75 42.88 41.89 7.00 6.50 1.01 1.18 6.12 7.55

N
150

 P
50

 K
0
 Z

0
137.63 144.00 129.42 125.25 38.50 40.46 6.67 6.75 1.07 1.30 6.87 7.20

N
150

 P
50 

K
0
 Z

5
138.22 147.32 125.25 121.75 42.88 42.88 6.67 7.25 0.94 1.17 6.25 7.50

N
150

 P
50

 K
50

 Z
0

137.93 144.60 124.40 120.50 41.50 44.13 7.25 7.62 1.07 1.16 6.75 7.50
N

150
 P

50
 K

50
 Z

5
137.11 153.50 122.50 120.25 44.00 45.13 7.33 7.75 1.13 1.33 6.87 7.95

C.D (P=0.05) NS 2.43 NS 1.91 1.51 0.54 NS 0.58 0.03 NS 0.07 0.88
NS: Not significant

J. Hort. Sci.
Vol. 1 (2): 129-134, 2006

Mineral nutrition & growth in tulip under polyhouse

131



page 132

may be attributed to this nutrient’s role in protein synthesis.
It is also an important part of chlorophylls, which are
involved in photosynthesis, and thus, in promoting plant
growth. Phosphorus is also an important constituent of many
essential compounds, and, is involved in various
physiological processes including cell division,
development of meristematic tissues, in photosynthesis,
respiration, etc. (Marschner, 1986). Phosphorus also
promotes root growth which, in turn, facilitates uptake of
other nutrients and results in improved growth. Growth
accelerating effects of potassium may be attributed to its
role as an activator of many enzymes and a major
contributor of plant osmotic relationship, essential for
stomatal movement and cellular growth (Salisbury and
Ross, 1986). Beneficial effects of zinc on physiological
activities might be the reason for improved plant growth. It
is an essential part of tryptophan, and thus, biosynthesis of
auxin which is known to promote cell elongation and root
initiation. Zinc is also an important constituent of several
vital enzymes that play a significant role in carbohydrate
synthesis (Marschner, 1986). Zinc also plays an important
role in the uptake of phosphorus and calcium and in the
availability of nitrogen (Shear, 1984).

Application of nitrogen caused significant increase
in days taken to flower, whereas phosphorus, potassium
and zinc resulted in significant decrease in days taken to
flowering compared to the control in both the years. This
finding is in accordance with the observation of earlier
workers (Sharma and Singh, 2001; Rani et al, 2005). Higher
doses of nitrogen may have caused excessive vegetative
growth adversely affecting days taken to flower. In many
species, days to flowering has been found to be closely
associated with nitrogen and phosphorus, as excess nitrogen
delays and abundant phosphorus hastens it. Contribution
of potassium and zinc in reducing days to may be due to
faster growth of the plant with application of these nutrients
and early completion of the vegetative phase (Khan, 2000;
Talukdar et al, 2003).

Scape length is an important quality parameter in
maintaining the post harvest life of cut flowers, whereas,
flower diameter is a parameter that influences aesthetic
appeal in a quality conscious world. Application of different
nutrients to soil individually exerted significant effects on
both scape length and tepal diameter in both the years of
experiment. Possible reasons for these effects might be
better nutrient uptake facilitated by phosphorus and zinc
and higher assimilation of food reserves through an

enhanced assimilatory surface. Scape length and flower size
have also been found to be positively correlated with
nitrogen dose in tuberose (Kumar and Singh, 1998). Kumar
and Arora (2000) reported higher spike length in gladiolus
with zinc application.

Addition of nitrogen, phosphorus and potassium
caused significant increase in vase life in cut tulip in distilled
water but zinc was unable to increase vase life in both the
years of experiment. Increase in vase life due to nutrient
treatment may be attributed to a healthy scape and leaves
which may have more food reserves to be utilized during
the vase period when the natural source of food is cut off
from the plant consequent to harvest. A healthy scape may
also facilitate better water uptake essential for maintaining
turgor, and thus, freshness of cut flowers. High potassium
level in the tissue may also have contributed directly to
maintaining turgor and thus resulted in increased vase life.

Like growth and flowering, bulb production
attributes were also influenced markedly by application of
various nutrients. The number of bulbs per plant was
significantly influenced by all the nutrients during the first

Table 3. Effect of N, P, K and Zn interactions on leaf N, P and K
content in tulip under polyhouse conditions

Treatment                            Nutrient concentration (%)
(kg ha-1)                Nitrogen             Phosphorus             Potassium

2002-03 2003-04 2002-03 2003-04 2002-03 2003-04

N
0
 P

0
 K

0
 Z

0
3.18 3.19 0.160 0.190 3.60 2.60

N
0
 P

0
 K

0
 Z

5
3.09 3.12 0.180 0.200 3.50 2.65

N
0
 P

0
 K

50
 Z

0
3.50 3.55 0.190 0.210 3.50 2.70

N
0
 P

0
 K

50
 Z

5
3.53 3.60 0.170 0.200 3.50 2.70

N
0
 P

50
 K

0
 Z

0
3.65 3.68 0.220 0.250 3.60 2.90

N
0
 P

50
 K

0
 Z

5
3.89 3.92 0.210 0.270 3.80 3.00

N
0
 P

50
 K

50
 Z

0
3.65 3.71 0.250 0.250 4.10 3.20

N
0
 P

50
 K

50
 Z

5
3.77 3.74 0.250 0.280 4.20 3.30

N
75

 P
0
 K

0
 Z

0
4.06 4.10 0.220 0.260 3.80 3.00

N
75

 P
0
 K

0
 Z

5
4.37 4.39 0.230 0.290 3.60 3.20

N
75

 P
0
 K

50
 Z

0
4.09 4.11 0.196 0.210 3.90 3.30

N
75

 P
0
 K

50
 Z

5
4.69 4.70 0.240 0.290 3.90 3.25

N
75

 P
50

 K
0
 Z

0
4.97 4.99 0.253 0.280 3.50 3.10

N
75

 P
50

 K
0
 Z

5
5.07 5.09 0.297 0.310 3.60 3.11

N
75

 P
50

 K
50

 Z
0

4.49 4.50 0.270 0.300 4.00 3.30
N

75
 P

50
 K

50
 Z

5
5.06 5.10 0.290 0.320 4.40 3.40

N
150 

P
0
 K

0
 Z

0
4.07 4.10 0.210 0.270 3.70 3.20

N
150

 P
0
 K

0
 Z

5
4.30 4.35 0.190 0.200 3.80 3.25

N
150

 P
0
 K

50
 Z

0
4.86 4.90 0.187 0.220 3.70 3.15

N
150

 P
0
 K

50
 Z

5
4.95 4.97 0.230 0.280 4.07 3.30

N
150

 P
50

 K
0
 Z

0
4.90 4.95 0.197 0.260 3.80 3.20

N
150

 P
50 

K
0
 Z

5
4.33 5.38 0.330 0.350 4.00 3.30

N
150

 P
50

 K
50

 Z
0

5.05 5.10 0.287 0.330 4.30 3.45
N

150
 P

50
 K

50
 Z

5
5.24 5.21 0.310 0.340 4.80 3.60

C.D (P=0.05) NS 0.35 0.05 NS NS NS

NS : Not significant

J. Hort. Sci.
Vol. 1 (2): 129-134, 2006

Khan et al

132



page 133

year while, during the second year, although nitrogen and
phosphorus showed significant effects, potassium and zinc
did not. All the nutrients had significant influence on the
weight of bulblets per plant. Application of nitrogen and
zinc has also been found to increase bulb production in
tuberose (Kumar and Singh, 1998) and dahlia (Khan, 2000),
respectively. A marked increase in both the number of bulbs
and bulblet weight per plant may be attributed to better
availability of phosphorus, which is  required in particularly
for bulb growth. Reduced bulb growth may be due to a
limitation of source because most of the photosynthates
tend to mobilize first towards the major sink i.e., flower.
Therefore, an increased assimilatory power might have
resulted in greater supply of photosynthates to the bulb,
thus, increasing its production.

Combined application of nutrients did not show any
marked impact on bulb survival per cent in both the years
(Table 2). Interaction treatments also failed to exert any
significant effect on stem thickness trials in both the years,
while wrapper leaf area was significantly influenced during
the 2nd year. Maximum wrapper leaf area (153.50 cm2) was
recorded with N

150
P

50
K

50
Z

5
 followed by N

150
P

50
K

0
Z

5
, while,

minimum was observed in N
0
P

0
K

0
Z

0 
(129.36 cm2)

. 
Like

wrapper leaf area, days taken to flowering also showed
significant influence when nutrients were applied in
combination, but only during the 2nd year of trial. The
minimum days taken to flower was 118.0 days in treatment
N

0
P

50
K

50
Z

5 
followed by N

75
P

50
K

50
Z

5 
against the maximum

(129.0) number of days in N
150

P
0
K

0
Z

0. 
Combined treatments

of nutrients also altered the scape length significantly in
both the years but did not exert any marked influence on
tepal diameter. Maximum scape length was recorded in
N

75
P

50
K

50
Z

5
 (44.25 cm) and N

150
P

50
K

50
Z

5 
(45.13 cm),

whereas, the minimum scape length was seen with
N

0
P

50
K

0
Z

0 
(33.88 cm and 30.66 cm) in first and second year,

respectively. Interaction effects of these nutrients on vase
life were non-significant during the first year, whereas, there
it differed significantly during the subsequent year with
maximum in N

75
P

50
K

50
Z

5
 (8.25 days) followed by

N
75

P
50

K
50

Z
0 

(8.00 days) and minimum in N
0
P

0
K

0
Z

0
 (6.12

days). Combination of different nutrient treatments affected
the number of bulbs per plant during the first year of trial
but did not show any marked variation in the subsequent
year. Treatment N

75
P

50
K

50
Z

5 
recorded the highest number

of bulbs per plant, (1.19) followed by N
75

P
50

K
50

Z
0
,
 
while, it

was minimum (0.88) in N
0
P

0
K

0
Z

0. 
However, both years of

experiment recorded a significant increase in bulblet weight
per plant due to combined effects of nutrients. The
maximum bulblet weight per plant observed was 8.12 g
(N

75
P

50
K

50
Z

5
) and 7.95 g (N

150
P

50
K

50
Z

5
), and, of 3.75 g and

4.20 g (N
0
P

0
K

0
Z

5
) during the first and second year of

experiment, respectively.

Nutrient analysis in leaf (Fig 1) revealed that
addition of nitrogen to soil significantly increased leaf
nitrogen content in both the years of experiment. However,
significant increase in phosphorus in the first year and
potassium level during the second year was observed.
Addition of phosphorus resulted in a marked increase in
leaf nitrogen, phosphorus and potassium content which
indicated that phosphorus was helpful in increasing uptake
of other nutrients from the soil. Phosphorus promotes root
growth, which in turn, facilitates improved uptake of other
nutrients (Marschner, 1986). Potassium application to the
soil also increased leaf nitrogen content significantly during
the first year of trial whereas increase in leaf nitrogen due
to potassium application in the subsequent year was not

J. Hort. Sci.
Vol. 1 (2): 129-134, 2006

Mineral nutrition & growth in tulip under polyhouse

133

Fig 1. Effect of N, P, K and Zn application on leaf nutrient content
in tulip

Fig 2. Month-wise relative humidity and temperature under
polyhouse conditions



page 134

significant. Increase in leaf potassium content due to
application of potassium in the soil is obvious because of
greater availability and uptake. Combined application of
nutrients exerted significant variation in leaf nitrogen and
phosphorus content during the 2nd and 1st year, respectively,
whereas potassium content of leaf remained unaffected
(Table 3).

Slight variations in the results of both years’ study
may be attributed to the differences in relative humidity
and temperatures during the growing periods of crops in
both years (Fig 2).

ACKNOWLEDGEMENTS

This research was supported by the Indian Council
of Agricultural Research, New Delhi, under the National
Agricultural Technology Project (Code No. C21183).

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