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The Influence Of Priming Two Cucumber Cultivar Seeds

The Influence Of Priming Two Cucumber Cultivar Seeds

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J. Duhok Univ. Vol.13, No.1, (Agri. And Vet. Sciences) Pp 1-18, 2010<br />

Company, US. Both cucumber cultivars were<br />

purchased from Agricultural Bureau, Mosul.<br />

A Split-Split Plot within Factorial<br />

Randomized Complete Block Design was<br />

adopted for this experiment. <strong>The</strong> main Plot (A)<br />

was the cultivation methods. <strong>The</strong>y represented<br />

by (i) - Direct seeds in permanent field when<br />

environment temperature was suitable for<br />

optimal growth (a1) and (ii) - <strong>Seeds</strong> were sown<br />

in plastic tea pots and kept in plastic-house until<br />

the ambient outdoor environment being suitable<br />

for sustaining optimal growth. <strong>The</strong>reafter they<br />

were planted in the permanent field (a2). <strong>The</strong> sub<br />

main plot was seed priming (B) was done as<br />

below:<br />

<strong>Seeds</strong> were unprimed (b1) and others were<br />

soaked for 24 hr. with 100% of their initial<br />

weights in distilled water (b2), -1.5 Mpa CaCO3<br />

(b3), -1.5 Mpa MgSO4 (b4), or -1.5 Mpa CaCO3+<br />

MgSO4 mixture (b5). <strong>The</strong> sub sub-main plot (C)<br />

was the cucumber cultivars where Babylon<br />

cultivar was (c1) and Khalifa cultivar was (c2).<br />

<strong>The</strong>n these seeds were rinsed and oven-dried at<br />

55 o C. for 72 hrs. to retain their initial weights.<br />

This hydrating-drying cycle was repeated three<br />

times. Thus (2x2x5=20) treatments were<br />

included in this experiment. Each treatment was<br />

replicated three times and a replicate was<br />

represented by a furrow of 1m width and 3m<br />

length planted on one side with 35 cm plant intra<br />

space. <strong>The</strong> very similar design was repeated in<br />

the second growing season (2005).<br />

Soaking solutions were prepared by<br />

dissolving the above chemical compounds in<br />

distilled water. <strong>The</strong> electrical conductivities of<br />

these solutions were measured by HANA<br />

ELECTRICAL CONDUCTIVITY DEVICE. <strong>The</strong><br />

osmotic potential was calculated by the<br />

following equation: OP Mpa = EC (dSm -1 ) x -<br />

0.36 (Ayers and Wescot, 1976). Field soil was<br />

clay (56.4% clay, 12.3% sand and 31.3% silt), its<br />

field capacity, wilting point and bulk density<br />

were 21.8%, 12.9% and 1.6 g.cm‾³, respectively.<br />

Soil was plowed vertically and horizontally,<br />

then, dissected to match the proposed design.<br />

<strong>Seeds</strong> of indirect cultivation were sown in<br />

teapots (filled with 1:1:1 peat moss: sheep<br />

manure: sand) inside the plastic house on March<br />

10, 2004. While in second season, seeds were<br />

sown on March 23, 2005. In first year trail,<br />

plants were transplanted in the permanent field<br />

on April 3, 2004 and on April 16, 2005 in<br />

second year trail, where plants possessed 4-6<br />

leaves. <strong>Seeds</strong> of direct cultivation were sown<br />

directly in the permanent field, at the date of<br />

2<br />

transplanting. Replanting was made on April 17,<br />

2004, since some plants of indirect cultivation<br />

were chilled and completely damaged. Plants<br />

were fertilized by NPK 27:27:0 four times at<br />

rates of 10 g.m -2 during the growing season. <strong>The</strong><br />

first application was done immediately after<br />

transplanting, while the others were during<br />

fruiting stage. Foliar spray of PhytoPhert<br />

micronutrients were also applied three times at a<br />

rate of 1.5 g.l -1 . <strong>The</strong> first was at flowering<br />

commencement and the other two were during<br />

fruiting stage. Weeds were eradicated manually<br />

whenever required around the growing season. A<br />

Mixture of 1 g.l -1 Benomyl fungicides and 2.5<br />

ml.l -1 Endosulfan insecticides was sprayed first<br />

on plants in the plastic house. This mixture was<br />

sprayed at the permanent field when plants<br />

possessed three actual leaves and three weeks<br />

latter to control powdery mildew and white fly.<br />

At any tabulated harvest fresh weight,<br />

numbers of fruits were taken. At the end of<br />

growing season on July 25, 2004 and July 29,<br />

2005 plants were pulled out, then brought to<br />

vegetable laboratory. Leaf number and branches<br />

number were counted. Leaf areas and plant<br />

lengths were measured. Leaves fresh weight,<br />

stem fresh weight, and plant fresh weight were<br />

weighed by sensitive metler balance. Samples of<br />

fruits, leaves, stems were weighed then ovendried<br />

at 65 o C for 72 hrs and finally reweighed.<br />

Fruit, stem, leaves, plant dry matter percentages<br />

besides leaf area index were calculated. Calcium<br />

content of fruits was determined according to<br />

procedure that recommended by Westerman<br />

(1990).<br />

RESULTS AND DISCUSSION<br />

<strong>The</strong> obtained results exhibited that indirect<br />

cultivation was superior on direct cultivation in<br />

2004. It substantially exceeded the latter in terms<br />

of plant fresh weight 16.4%, leaf dry weight<br />

41.1%, leaf fresh weight 29.2%, leaf number per<br />

plant 18.2% and total yield 23.3% (tables, 2 and<br />

4); fresh fruit yield at 3 rd , 4 th , 6 th , 9 th ,and 13 th ,<br />

respectively by 600.9, 220.8, 156.5, 62.5, and<br />

46.7% (table, 5); fruit number.m -2 at 4 th , 5 th , 6 th<br />

, and 9 th ,respectively by 236.4, 24.3, 168.9 and<br />

68.8% (table, 7). Like wise in 2005 indirect<br />

cultivation was significantly exceeded its<br />

corresponding direct cultivation in plant dry<br />

weight 11.3%, leaf dry weight 10.8%, and leaf<br />

fresh weight 29.7% (table, 3); fresh fruit yield<br />

g.m -2 at 6 th , 12 th , 14 th , 16 th , 17 th , 18 , 19 th and<br />

20 th by 96.4, 22.9, 81.4, 32.6, 77.2, 116.4, ∞ and

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