Crop growth studies
No significant results were observed in plant height at 1
st and 2
nd cut whereas at 3
rd cut significant increase in plant height was observed upto 40 kg K
2O ha
-1 over low levels of potassium and same trend was noticed at harvesting stage. No significant effect was observed on plant height at 1
st and 2
nd cut with boron levels but at 3
rd cut a significant increase in height was observed with 2 kg B ha
-1 over control (Table 1).
No significant increase was observed in number of tillers m
-2 at 1
st cut whereas, at 2
nd, 3
rd cut and at harvest significant improvement in tillers was observed with potassium application upto 40 kg K
2O ha
-1. Potassium an essential nutrient for the activation of enzymes like nitrogenase and nitrate reductase, responsible for the fixation of atmospheric nitrogen in the nodules as well as better nitrogen uptake might have contributed for better growth of the plants in terms of tiller number (Evans, 1954). Application of boron at 1
st cut marked non-significant effect, whereas at 2
nd and 3
rd cut, number of tillers m
-2 was significantly increased upto 2 kg B ha
-1 over control. Boron’s structural role in cell wall development and stimulation or inhibition of specific metabolism pathways and development of more meristematic tissues had lead to high number of tillers m
-2. At 2
nd cut and 3
rd cut, maximum number of tillers were observed with combination of 40 kg K2O ha
-1 and 2 kg B ha
-1.
Leaf–stem ratio remained unaffected at 1
st cut but at 2
nd and 3
rd cuts significant increase was found with application to 60 kg K
2O ha
-1 over control. Application of boron had no significant effect on leaf stem ratio at any of the cuts (Table 1).
Forage yield studies
The data presented in Table 2 revealed that potassium had a significant effect on green fodder yield of berseem at all the cuts. Green fodder yield increased significantly upto 40 kg K
2O ha
-1 at all the cuts and thus overall total green fodder. At 1
st cut, a significant effect of potassium was found on dry matter yield upto 40 kg K
2O ha
-1. Potassium plays an imperative role in the photosynthesis process and the subsequent carbohydrate translocation and metabolism, which eventually increase the crop yield
(Zorb et al., 2014). The results on green fodder and dry matter yields are in close conformity with the findings of
Aboelgoud et al., (2015) in berseem and Patel and Kotecha (2006) in lucerne. The crop had positively responded upto 2 kg B ha
-1 of boron application. Boron application at 1
st cut revealed non-significant effect but had significant influence on dry matter yield at 2
nd, 3
rd cuts and total dry matter yield. The favorable effect of boron in on yield may be owing to the important role of B maintenance of meristematic tissues and their activity and synthesis of N-bases such as uracil (Albert, 1968). These results are concurrent with the findings of Pradhan and Samant (1995) and Joshi and Bhilare (2006) in berseem. The crop was taken for seed purpose so at harvest stage after threshing crop for seed, straw was left instead of green fodder.
Interaction effects of potassium and boron levels on green fodder yield and dry matter yield at different cuts were noticed to be non-significant at I
st cut whereas, at II
nd, III
rd cut and total green fodder yield found to be significantly higher with the combination of 40 kg K
2O ha
-1 and 2 kg B ha-1 over other low levels (Table 3 and 4).
Effect on quality
An significant increasing trend in crude protein content and crude protein yield at 1
st cut was noticed with the increasing levels of potassium. Increase upto 60 kg K
2O ha
-1. No significant effect of B application was observed on crude protein content and yield at 1
st cut and 2
nd cut, however, significant increase in crude protein content and yield at 3
rd cut was observed with 4 kg B ha
-1 (Table 5). The physiological basis for such effects may be Involvement of boron in uracil synthesis, which is an essential component of RNA and in presence of boron, the ribosome are produced numerically, thereby the protein synthesis process was enhanced. The role of boron in protein synthesis has been also reviewed by Amberger (1975).
Price et al., (1972) also reported the possible role of boron in auxin metabolism, protein synthesis and phosphate utilization.
At 1
st cut, non-significant effect of potassium on IVDMD was observed. At 2
nd and 3
rd cuts significant effect was observed on IVDMD with the increasing potassium levels and highest IVDMD percentage was observed with the 40 kg K
2O ha
-1. Boron levels did not marked any significant effect on IVDMD at any of the cut (Table 6).
With different potassium levels significant effect on digestible dry matter yield was observed with 40 kg K
2O ha
-1, which was statistically at par with 60 kg K
2O ha
-1. Applied boron hadn’t marked any significant influence on the digestible dry matter yield (Table 6).
Economics
Highest gross returns were fetched at 60 kg K
2O ha
-1, whereas, maximum net returns and B:C ratio was worked out with 40 kg K
2O ha
-1. Overall, treatment with 0.2% spray at initiation and 50% flowering realized maximum B:C among both potassium and boron levels as quantity of boron used is less in this treatment which help in increasing seed yield which is expensive than fodder which lead to high gross and net returns (Table 7).