Agricultural Science Digest
Chief EditorArvind kumar
Print ISSN 0253-150X
Online ISSN 0976-0547
NAAS Rating 5.52
SJR 0.156
Chief EditorArvind kumar
Print ISSN 0253-150X
Online ISSN 0976-0547
NAAS Rating 5.52
SJR 0.156
The Effect of Intercropping of Lablab (Lablab purpureus L.) and Cowpea (Vigna unguiculata L.) at Different Planting Densities on in vitro and in sacco Dry Matter Digestibility of Napier Grass (Pennisetum purpureum)
Submitted30-07-2021|
Accepted15-12-2021|
First Online 16-01-2022|
Description of the study area
The study was conducted at Haro Sabu Agricultural Research Center during the main cropping season (Fig 1). The center is located in western Ethiopia at 550 km from Addis Ababa. It lies at latitude of 8°52'51" N and longitude 35°13'18" E and altitude of 1515 m.a.s.l. It has a warm humid climate with average minimum and maximum temperature of 14 and 30°C respectively (HSARC, 2012). The area receives average annual rainfall of 1000 mm and its distribution pattern is uni-modal (HSARC, 2012) (Table 1). The main rainy season covers from April to October. The soil type of the experimental site was vertisol with sandy loam in texture (Abebe, 2007). The area is characterized by coffee based farming and crop-livestock mixed farming system (HSARC, 2012).
Experimental layout, design and treatments
The experimental design was factorial combination arrangement in RCBD with three blocks consisting of three levels of inter and intra row spacing of Napier grass (ILRI 16840 accession ) i.e. 0.5 m × 0.5 m, 0.75 m × 0.5 m and 1 m × 0.5 m intercropping with two tropical forage legumes of cowpea (Vigna unguiculata L.) Bole variety and Lablab (Lablab purpureus L.) 14455 accession between the rows of Napier grass and totally nine treatments were used (Table 2).
Data collected
In vitro dry matter digestibility
Chemical analysis was used performed on all for samples used in vitro dry matter digestibility (IVDMD). The two-stage rumen inoculates pepsin method of Tilley and Terry (1963) was used to determine IVDMD. Rumen liquor was collected from three rumen fistulated steers and transported to the laboratory using thermos flask that have been pre-warmed to 39°C. Rumen liquor was taken in the morning before animals were offered feed. A duplicate sample 0.5 g each was incubated with 30 mL of rumen liquor in 100 ml test tube in water bath at 39°C for a period of 48 h for microbial digestion followed by another 48 h for enzyme digestion with acid pepsin solution. Blank samples containing buffered rumen fluid were incubated in duplicates for adjustment. Drying of samples residues were done at 105°C for 24 h. The samples were then ashed to estimate IVOMD. An IVOMD analysis was carried out at Holeta Agricultural research center animal feed analytical laboratory.
Metabolisable energy (ME) was calculated from IVOMD using the equation:
ME (MJ kg-1 DM) = 0.15*IVOMD (Pinkrton, 2005)
In sacco digestibility
In sacco digestibility was carried out at Holeta Agricultural Research Center Animal Nutrition Analytical Laboratory. Composite samples of Napier grass for each treatment were taken and dried in a forced draft oven at 60°C for 72 h. Samples were ground and passed through a 2 mm screen (mesh) using Wiley mill for in Sacco digestibility.
A numbered Nylon bag with 6.5 × 14 cm2 dimension with a pore size of 41 mm was taken into an oven and dried at 60-65°C for 30 minutes. Contented was weighed immediately or after allowing to cool to room temperature in a desiccators and 3.0 g of dried forage samples were tightly packed using nylon string which is resistant to rumen micro-organisms and then taking in three rumen fistulated steers for 0, 6, 12, 24, 48, 72 and 96 h. Each feed sample was incubated in duplicate in the three steers for any one incubation time. At the end of each incubation hours, all the bags (including the zero hour samples) were immediately washed with cold water for about 30 minutes under running tap water while rubbing gently between thumb and fingers until the water runs clear and then the washed bags were dried in an oven at 60-65°C for about 48 hours. Duplicate bags of each sample were washed without incubating in the rumen in order to determine the washing loss. The dried bags were then taken out of the oven and allowed to cool down in desiccators and weigh immediately.
The digestibility or disappearance of DM (DMD) and OM (OMD) of each incubation time were determined as (AOAC, 1990).
Where,
SWa = Weight of the original sample + nylon bag.
BW = Weight of empty nylon bag.
DMa = Dry matter of feed sample.
DMb = Dry matter of residue sample.
SWb = Weight of the sample + nylon bag after incubation.
The DMD and OMD values at various times of incubation are fitted to the exponential equation:
p = a + b (1 - e-ct)
Where
a = Washing loss (rapidly soluble fraction).
b = Slowly degradable fraction.
c = The rate of degradation.
e = The natural logarithm.
p = The potential disappearance of DM / OM at time t.
t = Time as described by Ørskovet_al(1981) using the Neway Excel programme (Chen, 1995).
The potential degradability (PD) was estimated as:
PD = a + b
whereas the effective degradability of DM and OM (ED) was calculated using (Ørskov and McDonald, 1979) formula:
ED = a + [(b*c)/(c + k)] at 0.03/hour for grass rumen out flow rate (k). Where a, b and c are as described above and k = passage rate.
Statistical analysis
Data were subjected to ANOVA procedure by using SAS software version 9.3 (Littell et al., 2002). Significant means were separated and compared using Least Significant Difference (LSD) test at 5% significant level. The analysis of variance model for the in sacco degradability parameters were:
Y ij = μ+ Ti + Ai + eij
Where,
Yij = Individual observation.
μ = Overall mean.
Ti = Treatment effect.
Ai = Animal effect.
Eij = Residual error.
In vitro digestibility
In vitro dry matter digestibility
Napier grass at different planting densities intercropped with lablab and cowpea had significant effect (P<0.05) on the in vitro dry matter digestibility (IVDMD) (Table 3). Napier grass intercropped with lablab (T7) and cowpea (T4) at spacing of 1 m × 0.5 m has highest IVDMD with the mean result of (64.85±1.99%) and (66.92±0.66%) value, respectively while other mean comparisons were not significant (P>0.05). On the other hand, sole Napier grass planted at plant spacing of 0.5 m × 0.5 m (T9) had the lowest value of the IVDMD and IVDMD increased with wider spaces of Napier grass in the sole and intercropped at three different planting densities. The result noted by Bayble et al., (2007) for IVDMD of Napier grass at spacing of 1 m × 0.5 m intercropped with lablab harvested at 90 days was (68%) and it was higher than the mean result (64.85±1.99%) for Napier grass at 1m × 0.5m space intercropped with lablab of the present finding. Such variation could be associated with various factors like rain, humidity, light and temperature, soil fertility and other management practices have an influence on IVDMD of Napier grass (Assefa and Ledin, 2001).
Analysis of variance showed that there was a significant effect (P<0.05) of Napier grass intercropping with lablab and cowpea at different planting densities on in sacco organic matter disappearances (OMD) at 6, 48 and 96 h of incubation time but No significant differences (P>0.05) were observed at the rest of hours of incubation time (Table 6).
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