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Production Practices and Quality Assessment of Food Crops. Vol. 1

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182 Chris A. Shisanya<br />

Table 11. N concentration at harvest in TB plant tissues during the LR season 1999 <strong>and</strong> SR season<br />

<strong>of</strong> 1999/2000.<br />

Treatment LR season 1999 SR season 1999/2000<br />

Shoot Root Seed Shoot Root Seed<br />

———————— N concentration (mg N/g dry matter) ————————<br />

TB+N* 1.5 b 0.6 b 2.5 b 1.5 b 0.8 b 2.5 b<br />

Control 1.1 b 0.5 b 2.0 b 1.3 b 0.6 b 2.0 b<br />

TB + R3254 2.3 a 1.8 a 3.8 a 2.1 a 2.0 a 3.8 a<br />

TB + R446 1.7 b 0.8 b 2.9 b 1.5 b 0.9 b 2.8 b<br />

TB + RTB 1.6 b 0.6 b 2.8 b 1.5 b 0.8 b 2.9 b<br />

TB + R578 1.3 b 0.7 b 2.3 b 1.4 b 0.7 b 2.5 b<br />

TB + R579 1.5 b 0.8 b 2.4 b 1.5 b 0.9 b 2.3 b<br />

Means (n = 4) followed by the same letter down the column are not statistically different (P ≤ 0.05)<br />

by Duncan’s multiple range test.<br />

* Nitrogen (N) fertilizer was top-dressed 10 DAE at the rate <strong>of</strong> 40 kg ha –1 <strong>of</strong> CAN (26% N) powder.<br />

above the threshold (50 rhizobia cells per gram <strong>of</strong> soil) at which inoculation may<br />

be excluded (Thies et al., 1991). The soils were collected during the dry season<br />

<strong>and</strong> it is also expected that during the rains rhizobia along with other soil microorganisms,<br />

Rhizobia population number would increase (Gitonga et al., 1999; Maingi<br />

et al., 2001). These results support the findings <strong>of</strong> Nambiar et al. (1983) that most<br />

tropical soils have rhizobial population <strong>of</strong> at least 100 rhizobia cells per gram <strong>of</strong> soil<br />

capable <strong>of</strong> nodulating the legumes grown in such soil.<br />

The number <strong>of</strong> nodules on the tepary bean in all the treatments was counted<br />

regardless <strong>of</strong> their size. The greenhouse results (Table 4) obtained on nodulation<br />

indicated that tepary bean inoculated with Rhizobium strains R3254, RTB <strong>and</strong><br />

R446 had good nodulation, while those inoculated with strains R578, R579 <strong>and</strong> N<br />

treatment had poor nodulation. There was no nodulation in the control treatment.<br />

Overall, treatment R3254 had significantly higher (P ≤ 0.05) nodule number than<br />

the other treatments (Table 4). These nodules were effective in N 2 fixation as<br />

evidenced by the pink colouration <strong>of</strong> the nodules indicating the presence <strong>of</strong><br />

leghaemoglobin (Sprent <strong>and</strong> Sprent, 1990; Amara et al., 1995;). Nodule number is<br />

always used as a measure <strong>of</strong> infectiveness (Beck et al., 1993). The high number<br />

<strong>of</strong> nodules per plant in tepary bean inoculated with strain R3254 was evidence for<br />

the high infectiveness <strong>of</strong> this particular Rhizobium strain.<br />

The plant test is the only confirmatory test for rhizobia (Vincent, 1970). Glass<br />

growth tubes were used for plant tests. This method, besides the Leonard jar<br />

assembly, has become a st<strong>and</strong>ard method for testing nodulation <strong>and</strong> nitrogen fixation<br />

under greenhouse conditions (Beck et al., 1993). The method is economical in water<br />

use <strong>and</strong> reduces the chances <strong>of</strong> bacterial contamination (Beck et al., 1993). The tubes<br />

occupy very little space in the greenhouse <strong>and</strong> provide good depth for growth <strong>and</strong><br />

development <strong>of</strong> roots. Nitrogen production due to algae growth on media <strong>and</strong> in<br />

water has been shown to be minimal (Hornetz et al., 2000). Plant dry weight was<br />

used indirectly to estimate N 2 fixation in the present study. This method is the

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