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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 94-102, 2010<br />

irrigation during all physiological stages (Abdel,<br />

1993). <strong>The</strong> superiority of Aqualduce and Local<br />

Syrian cultivars under water scarcity could be<br />

attributed to their genetic which reflected the<br />

highly performed breeding techniques that had<br />

been implicated during screening of the<br />

produced seeds by their producing companies.<br />

Taka357 is a determinate cultivar of a small<br />

vegetative growth possesses little number of<br />

leaves composed of broad leaflets; however,<br />

high leaf area was inadequate to brought about<br />

high leaf area index to compensate with these of<br />

indeterminate cultivars. Land coverageratio of<br />

determinate cultivars are lower that of<br />

indeterminate cultivars which make them more<br />

vulnerable to both high irradiance and<br />

evapotranspiration adversity and of low<br />

competition abilities. Subsequently these<br />

Newblack fly and Tiger cultivars were not<br />

recommended under drought (Abdel, 1982).<br />

Water stressed Aquadulce plants sprayed<br />

by 2x10 -3 M ABA manifested the highest plant<br />

height (80.5 cm), node number on main stem<br />

(19.33). When this cultivar was sprayed by 2x10 -<br />

49<br />

6 M ABA, it exhibited the highest leaflet number<br />

per plant (264.67) and plant fresh weight (137.33<br />

g). In addition to that untreated Aquadulce<br />

showed the highest plant dry weight (19.87 g).<br />

<strong>The</strong> highest internodes length (5.55 cm) and<br />

individual leaf area (20.96 cm) were confined to<br />

Taka 357 sprayed by 2x10 -6 M ABA. While the<br />

highest number of branches per plant (6.33) was<br />

observed in untreated Taka 357 (table, 1). <strong>The</strong><br />

obtained results suggested that cultivar responses<br />

were more overwhelmed by their genome rather<br />

than by ABA. <strong>The</strong>re are three reasons that<br />

reinforce this phenomenon; the first is that ABA<br />

imparted temporary elastic (not plastic) changes<br />

in stomata sizes, since ABA was sprayed<br />

immediately after re-watering. <strong>The</strong> second<br />

reason is that ABA application and drought<br />

acquired the stomata degree of adaptation which<br />

enabled them to cope with further high leaf<br />

content of ABA (Davies, 1978). <strong>The</strong> third reason<br />

could be referred to hormonal balance during<br />

juvenility, in which active ABA undergoes a<br />

conversion into inactive ABA for instance<br />

dihydrophaseic acid (Srivastava, 2002).<br />

Table (1): <strong>The</strong> effects of varying abscisic acid (ABA) rates on some growth traits of five water stressed fababean cultivars* **<br />

Parameters P h (cm) B no N no L no L a (cm -2 ) L in In l Pdw Pfw<br />

Aquadulce 71.15a 4.44ab 18.22a 240.56a 13.82b 4.46a 3.95b 15.47a 126.78a<br />

Syrian 64.75a 4b 18.11a 212ab 13.61b 3.88ab 3.59bc 13.22ab 125.11a<br />

Taka357 41.14c 5.44a 7.55b 108.66c 19.04a 2.77b 5.5a 9.14c 119.22a<br />

<strong>Two</strong>waytha 65.6a 3.55b 17.11a 180.56b 12.12b 2.8b 3.82bc 11.44bc 110.11ab<br />

Babylon 55.71b 3.44b 17.11a 179b 12.79b 3.07b 3.25c 8.81c 91.22b<br />

0.0 ABA 54.35a 4.46a 14.66a 187.33a 13.01a 3.11a 3.6a 13.08a 116.73a<br />

2x10 -6 M ABA 58.76a 4.26a 15.53a 190.67a 15.04a 3.59a 3.98a 11.59a 122.87a<br />

2x10 -3 M ABA 65.91a 3.8a 16.66a 174.47a 14.78a 3.48a 4.13a 10.17a 103.87a<br />

Aqudulce<br />

Syrian<br />

Taka 357<br />

<strong>Two</strong>waytha<br />

Babylon<br />

0.0 M 61.8 bd 4.33ac 17.33a 232.67ab 14.49ad 4.48ac 3.74bc 19.87a 132.67a<br />

2x10 -6 M 71.16ac 5ab 18a 264.67a 12.02cd 4.26ac 3.95bc 14.42ab 137.33a<br />

2x10 -3 M 80.5a 4bc 19.33a 224.33ad 14.95ad 4.65ab 4.16b 12.11b 110.33ab<br />

0.0 M 66.2ac 3.66bc 17.33a 193.33be 13.05bd 3.33ac 3.82bc 15.17ab 127.33a<br />

2x10 -6 M 61.86bd 4bc 18.33a 213.33ad 12.12cd 3.52ac 3.38bc 11.86b 126a<br />

2x10 -3 M 66.2ac 4.33ac 18.66a 229.33ac 15.66ac 4.82a 3.56bc 12.62b 122ab<br />

0.0 M 37.5f 6.33a 7b 117.33fg 19.25ab 3.07ac 5.5a 9.79b 119.67ab<br />

2x10 -6 M 39.8f 5ab 7.33b 9.33g 20.96a 2.75ac 5.46a 9.23b 120ab<br />

2x10 -3 M 46.13ef 5ab 8.33b 109.33fg 16.92ac 2.48bc 5.55a 8.42b 118ab<br />

0.0 M 59.13be 4.66ac 15.33a 225.33ad 8.27d 2.46bc 3.87bc 11.84b 108.33ab<br />

2x10 -6 M 63.46bc 3.33bc 17.33a 169.67bf 15.35ac 3.41ac 3.62bc 12.67b 121.67ab<br />

2x10 -3 M 74.2ab 2.66 18.66a 146.67fg 12.73bd 2.52bc 3.97bc 9.82b 100.33ab<br />

0.0 M 47.13df 3.33bc 16.33a 168cf 10cd 2.23c 2.89c 8.73b 95.67ab<br />

2x10 -6 M 57.5ce 4bc 16.66a 206.33ae 14.76ad 4.02ac 3.47bc 9.79b 109.33ab<br />

2x10 -3 M 62.5bc 3.3bc 18.33a 162.67df 13.62bd 2.95ac 3.39bc 7.9b 68.67b<br />

** Ph = plant height; B no = branches number per plant: N no = node number on main stem: L no = leaflet<br />

number per plant: L a = leaflet area: L in = leaf area index: In l = internodes length:<br />

Pdw = plant dry weight (g.plant -1 ):<br />

Pfw = plant fresh weight (g.plant -1 ).<br />

* Figures of unshared characters are significant (Duncan, 0.05)

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