01.06.2015 Views

Effects of arbuscular mycorrhizal inoculation on the growth, photosynthetic pigments and soluble sugar of Crocus sativus (saffron) in autoclaved soil

The beneficial soil microorganisms as arbuscular mycorrhizal fungi (AMF) form the mutualistic relationship with plant roots and act as bio fertilizers for saffron (Crocus sativus L.). In the present study, the plant growth, AMF colonization and nutrient uptake of C. sativus evaluated in earthen pots filled with sterile soil. C. sativus seedlings with or without AMF spores of the Glomus species, were cultivated for six months in autoclaved sediment medium. The results of the first year showed a significant increase of the above and below ground growth of saffron plant. The fresh and dry weight content indicated in higher levels of inoculated group that the value of biomass was 4.05 (gr) and 0.42 (gr) than non-inoculated group, respectively. The photosynthetic pigments and soluble sugar content increased in the mycorrhiza infected as compared to the non-inoculated ones with rate of 36.69% and 43.1%, respectively. In addition, the mycorrhizal dependency (MD) of C. sativus to AMF reached a maximum of 38.18% under AMF inoculation treatment, which was significant (p < 0.05).

The beneficial soil microorganisms as arbuscular mycorrhizal fungi (AMF) form the mutualistic relationship with plant roots and act as bio fertilizers for saffron (Crocus sativus L.). In the present study, the plant growth, AMF
colonization and nutrient uptake of C. sativus evaluated in earthen pots filled with sterile soil. C. sativus seedlings with or without AMF spores of the Glomus species, were cultivated for six months in autoclaved
sediment medium. The results of the first year showed a significant increase of the above and below ground growth of saffron plant. The fresh and dry weight content indicated in higher levels of inoculated group that the value of biomass was 4.05 (gr) and 0.42 (gr) than non-inoculated group, respectively. The photosynthetic pigments and soluble sugar content increased in the mycorrhiza infected as compared to the non-inoculated ones with rate of 36.69% and 43.1%, respectively. In addition, the mycorrhizal dependency (MD) of C. sativus to AMF reached a maximum of 38.18% under AMF inoculation treatment, which was significant (p < 0.05).

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weight <str<strong>on</strong>g>of</str<strong>on</strong>g> root (150 mg) mixed with 70% ethanol.<br />

Then <strong>the</strong> phenol reagent <strong>and</strong> sulphuric acid were<br />

added <strong>and</strong> <strong>the</strong> soluti<strong>on</strong>s were <strong>in</strong>cubated at room<br />

temperature for 30m<strong>in</strong> <strong>and</strong> <strong>the</strong> UV absorbance was<br />

read at 485nm. Glucose was used as <strong>the</strong> st<strong>and</strong>ard for<br />

this analysis.<br />

Data analysis<br />

The experiment was laid out as a completely<br />

r<strong>and</strong>omized design, with five replicates <str<strong>on</strong>g>of</str<strong>on</strong>g> each<br />

treatment. Data were analyzed us<strong>in</strong>g a statistical<br />

package, SPSS versi<strong>on</strong> 16.0. One-way analysis <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

variance (ANOVA) followed by <strong>the</strong> t-test (h<strong>on</strong>estly<br />

significant difference, p < 0.05) were carried out to<br />

determ<strong>in</strong>e differences between means. Correlati<strong>on</strong><br />

analysis was carried out by two-tailed Pears<strong>on</strong> test,<br />

with p < 0.05 as <strong>the</strong> correlati<strong>on</strong> degree. All data were<br />

plotted us<strong>in</strong>g Orig<strong>in</strong> 8.0 s<str<strong>on</strong>g>of</str<strong>on</strong>g>tware.<br />

Results<br />

AMF root col<strong>on</strong>izati<strong>on</strong><br />

Our <strong>in</strong>vestigati<strong>on</strong> <strong>in</strong>dicated no AMF structures <strong>in</strong><br />

n<strong>on</strong>-<str<strong>on</strong>g>mycorrhizal</str<strong>on</strong>g> <str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> treatments. In <strong>the</strong> AMF<br />

<str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> treatment, all plant roots showed<br />

associati<strong>on</strong>s with AMF. Intracellular hyphae <strong>and</strong><br />

<str<strong>on</strong>g>arbuscular</str<strong>on</strong>g> were <strong>the</strong> dom<strong>in</strong>ant structures, <strong>and</strong> <strong>the</strong><br />

<str<strong>on</strong>g>arbuscular</str<strong>on</strong>g> structure was ‘Arum’ type (Fig. 1). The<br />

PRC <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> <strong>in</strong>oculated AMF (<strong>in</strong>clud<strong>in</strong>g Glomus<br />

etunicatum, G. mosseae, <strong>and</strong> G. aggregatum)<br />

calculated 39% (p < 0.05).<br />

Table 1. Effect <str<strong>on</strong>g>of</str<strong>on</strong>g> n<strong>on</strong>-<strong>in</strong>oculated <strong>and</strong> <strong>in</strong>oculated <strong>soil</strong>s <strong>on</strong> chlorophyll <strong>and</strong> carotenoids (mg.g -1 FW) <str<strong>on</strong>g>of</str<strong>on</strong>g> C. <strong>sativus</strong><br />

plant <strong>in</strong> pot experiment.<br />

Group No. <str<strong>on</strong>g>of</str<strong>on</strong>g> pots Chl.a Chl.b Carotenoid Chl.a + Chl.b Chl.a /Chl.b Chl.a + Chl.b/<br />

Carotenoid<br />

N<strong>on</strong>-<strong>in</strong>oculated (NG) 5 0.752 0.371 0.385 1.123 2.027 2.917<br />

Inoculated (IG) 5 1.12 0.654 0.576 1.774 1.713 3.08<br />

Enhanced plant <strong>growth</strong> resp<strong>on</strong>se<br />

Significant <strong>in</strong>crease <strong>in</strong> rate <strong>and</strong> total emergence <str<strong>on</strong>g>of</str<strong>on</strong>g> C.<br />

<strong>sativus</strong> seedl<strong>in</strong>g <strong>in</strong> <strong>soil</strong> treated with AMF <str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g><br />

were observed (Fig. 2). Sizes <str<strong>on</strong>g>of</str<strong>on</strong>g> emerged plant <strong>in</strong> <strong>soil</strong><br />

<strong>in</strong>fested with AMF <str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> were more uniform<br />

than those <str<strong>on</strong>g>of</str<strong>on</strong>g> c<strong>on</strong>trol plant. In additi<strong>on</strong>, <strong>the</strong> plant<br />

height <str<strong>on</strong>g>of</str<strong>on</strong>g> C. <strong>sativus</strong> differed significantly under AMF<br />

<str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> (p < 0.05). In AMF <str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> treatment<br />

group, plant height reached a maximum <str<strong>on</strong>g>of</str<strong>on</strong>g> 27.61 cm,<br />

which was 35.8% higher than <strong>the</strong> c<strong>on</strong>trol.<br />

<strong>and</strong> dry weight compared to c<strong>on</strong>trol, respectively. The<br />

<str<strong>on</strong>g>mycorrhizal</str<strong>on</strong>g> dependency (MD) <str<strong>on</strong>g>of</str<strong>on</strong>g> C. <strong>sativus</strong> to AMF<br />

reached a maximum <str<strong>on</strong>g>of</str<strong>on</strong>g> 38.18% under AMF<br />

<str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> treatment, which was significant (p <<br />

0.05)<br />

Biomass <strong>and</strong> MD <str<strong>on</strong>g>of</str<strong>on</strong>g> C. <strong>sativus</strong><br />

The results <str<strong>on</strong>g>of</str<strong>on</strong>g> pot study showed that <str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> C.<br />

<strong>sativus</strong> seedl<strong>in</strong>g with AMF affected root <strong>and</strong> shoot<br />

fresh weight (Fig. 3). Total Shoot fresh weight<br />

significantly <strong>in</strong>creased by <str<strong>on</strong>g><strong>in</strong>oculati<strong>on</strong></str<strong>on</strong>g> <strong>in</strong> sterile <strong>soil</strong>,<br />

which was 3.14 g higher than <strong>the</strong> c<strong>on</strong>trol (5.02 g)<br />

(p

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