MEKARN Regional Conference 2007: Matching Livestock Systems with Available Resources |
The four treatments applied to 4 growing pigs (15 kg live weight) in a 4*4 Latin square arrangement were four levels of ensiled leaves of taro (Colocasia esculenta) equivalent to 25, 50, 75 and 100% substitution of the protein from fish meal in a basal diet of sugar palm syrup. The pigs were housed in metabolism cages for consecutive periods of 12 days, with collection of faeces and urine during the last 5 days of each period.
There were positive curvilinear trends in DM and crude protein
intake and in N retention in response to replacement of fish meal
by ensiled taro leaves with the optimum proportion being at about
70-75% replacement. Coefficients of DM apparent digestibility were
high on all diets but those for crude protein showed a negative
curvilinear response with declining values beyond 25% substitution
of the fish meal protein by that from taro leaf silage. The
limiting factor to utilization of the taro leaf silage appears to
be the lower apparent digestibility of the protein in the taro
leaves.
Taro (Colocasia esculenta), also known as "Old Cocoyam", is a wetland crop in many tropical and subtropical areas of the world, cultivated mainly for root (corm) production. Before the corm can be eaten, the traditional practice is to cook it so as to break down the needle-like calcium oxalate crystals which are present in all parts of the plant. According to Miller (1929), these crystals are "extremely irritating to the throat and mouth lining, causing a burning and stinging sensation". Many other plants contain substantial quantities of oxalate (Standal 1983). Proposed functions of the oxalate content in plants are said to include: protection from insects and foraging animals through toxicity and/or unpalatability, osmo-regulation, and regulation of calcium levels in plant organs and tissues (Libert and Franceschi 1987).
In a survey in Takeo and Pursat provinces, 51% of the farmers that were interviewed reported feeding the petiole of Taro (Paper I) to pigs. As for the corm, the traditional practice is to boil the petioles before feeding. Very few farmers reported feeding the leaves. In the mountain areas of North Vietnam, there is a tradition of using both the corm and the leaves of Giant taro (Alocasia macrorrhiza) as feed for pigs (Tiep et al 2006). As in the case of taro, it was reported (Tiep et al 2006) that the traditional way is to boil the corm and the leaves prior to feeding, as this reduced the concentration of calcium oxalate present. These authors showed that ensiling the leaves with rice bran and molasses reduced the calcium oxalate content by 78%, and that the silage could be included in the diet of growing pigs at the 10% level without affecting growth rate. In Colombia, Rodriguez et al (2006) showed that the leaves of the New Cocoyam (Xanthosoma sagittifolium) could be fed fresh to young pigs at levels replacing 50% of the soybean meal (approximately 45% of the diet DM) and that growth rates (500 g/day) were similar to those on the control diet without the leaves. The leaves were chopped before offering them to the pigs which may have reduced the oxalate content as it was observed that the irritating effect from handling the leaves was reduced after chopping them (Preston T R personal communication).
There appears to be little recent research on the feeding value
of taro leaves for pigs. For this reason the present study was
carried out to provide preliminary information on digestibility and
nitrogen balance in pigs fed ensiled taro replacing fish meal,
using a fibre-free basal diet (sugar palm syrup), as according to
Preston (2006) this is likely to facilitate the use of fibrous
protein sources, such as leaves from vegetative sources.
The experiment was conducted in the ecological farm of the Center for Livestock and Agriculture Development (CelAgrid), located in Rolous village, Rolous commune, Kandal Stoeung district, Kandal province, about 26 km from Phnom Penh City, Cambodia. During the trial (from 1 September to 21 November 2006), the average ambient temperature was 25.9 ± 0.96 C in the morning at 06:00h, 31.7 ± 1.59 C in the middle of day, and 28.3 ± 1.90 C in the afternoon at 18.00h.
The experiment was carried out as a Latin Square 4x4 arrangement with 4 pigs and 4 periods (Table 1), each of 12 days. The first 7 days were for adaptation to the diet, followed by 5 days for collection of faeces and urine.
Table 1. Experimental layout of the digestibility trial |
||||
Period |
Pig 1 |
Pig 2 |
Pig 3 |
Pig 4 |
1 |
TS25 |
TS50 |
TS75 |
TS100 |
2 |
TS100 |
TS75 |
TS50 |
TS25 |
3 |
TS75 |
TS100 |
TS25 |
TS50 |
4 |
TS50 |
TS25 |
TS100 |
TS75 |
Four crossbred (Large White x Local) castrated male pigs,
initially averaging 15.0 ± 1.0 kg live weight were used for
the experiment. They were housed in metabolism cages (1.6 x 1.4 m
floor area), elevated 0.6 m and allowing the separate collection of
faeces and urine. The cages were made of wood and were situated in
a building with a thatch roof of Imperata grass, and open
sides.
Wild taro (Trav Prey) leaves were harvested from a lake receiving waste water from Phnom Penh City. The leaves were chopped into small pieces and ensiled with 5% of sugar palm syrup (79% of DM) and 2% of water (fresh basis) to facilitate the mixing of the viscous syrup. Leaves and syrup (plus the water) were carefully mixed and stored in plastic bags, inside rigid plastic containers. The bags were tightly closed to prevent air contact and stored for 30 days before feeding. Every container thus prepared contained approximately 150 kg of fresh material. The ensiled Taro leaves had a pH of 3.85 after one month and DM content of 18.3%.
Four diets were formulated with protein from ensiled taro leaves replacing fish meal protein at levels of 25, 50, 75 and 100% (Table 2). The pigs were fed ad libitum, with fresh feed supplied 3 times per day during the adaptation period, and given 80% of the mean ad libitum intake in the collection period to avoid residues. All ingredients were mixed together before feeding. Fresh water was available at all times from nipple drinkers. The duration of the experiment was 48 days.
Table 2. Chemical composition of ensiled taro leaves and ingredient and chemical composition of the experimental diets (% in dry matter) |
|||||||
|
Ensiled taro leaves |
Fish meal |
Sugar palm syrup |
Replacement of fish meal protein, % |
|||
25 |
50 |
75 |
100 |
||||
Ingredients,% |
|
|
|
|
|
|
|
Ensiled taro leaves |
- |
- |
- |
11.5 |
23 |
34.5 |
46 |
Fish meal |
- |
- |
- |
25.0 |
16.8 |
8.4 |
0 |
Sugar palm syrup |
- |
- |
- |
62.0 |
58.7 |
55.6 |
52.5 |
Salt |
- |
- |
- |
0.5 |
0.5 |
0.5 |
0.5 |
Premix (mineral-vitamin) |
- |
- |
- |
1.0 |
1.0 |
1.0 |
1.0 |
Analytical data calculated from analysis of the ingredients |
|||||||
Dry matter % |
18.3 |
92.1 |
79 |
75.4 |
67.4 |
59.3 |
51.2 |
As % of DM |
|||||||
Ash |
8.3 |
56.8 |
0.02 |
15.2 |
11.5 |
7.63 |
3.81 |
Crude protein |
25.9 |
35.6 |
0.24 |
12 |
12 |
12 |
12 |
Calcium oxalate |
0.11 |
- |
- |
0.013 |
0.025 |
0.038 |
0.051 |
Feeds offered and residues, and output of faeces and urine were recorded daily during the last 5 days of each period. The animals were weighed in the morning before feeding at the beginning and the end of each period. Samples of each component (offered) were retained for analysis of DM, Ash, OM and N. A sub-sample (10%) of faeces was put each day in plastic bags in the freezer (-20 °C). Urine was collected in a bucket containing 10 ml of 10% sulphuric acid (H2SO4) to keep the pH below 4 so as to prevent escape of ammonia. A sub-sample (10%) was collected each day and kept in the freezer.
Feed and faecal samples were dried by microwave radiation to measure the DM content (Undersander et al 1993). Total N of samples of feed and faeces and urine was determined by the Kjeldahl procedure as outlined in AOAC (1990). The ash content of feed and faeces was determined following the AOAC (1990) recommendations; organic matter was assumed to be the result of subtracting the percentage of ash from 100. The calcium oxalate was determined according to AOAC (1990) procedures.
The data were analyzed using the general linear model (GLM)
procedure in the ANOVA software of MINITAB (release 13.31). Sources
of variation were treatments, periods, animals (pigs) and
error.
The process of ensiling the taro leaves was more effective than sun-drying in reducing the calcium oxalate content (Table 3). The concentration in the ensiled leaves was lower than reported by Tiep et al (2006) (0.7% in DM) for ensiled leaves of Giant taro (Alocacia macrorrhiza). The fish meal used was of extremely poor quality, with a crude protein content of only 35.6% of DM, and an ash content of 56.8%, probably because the meal was contaminated, possibly by, for example, addition of sand.
Table 3. Effect of sun-drying and ensiling on calcium oxalate in the taro leaves, % in DM |
||
Fresh |
Sun-dried |
Ensiled |
3.08 |
1.10 |
0.11 |
There were slight differences between the planned and observed levels of substitution of fish meal protein by the protein from taro leaves, with higher than intended levels for the intermediate treatments TS25, TS50, and TS75 (Table 4). This was because of a small degree of selection by the pigs.
Table 4. Proportions (%) of the protein supplement provided by taro leaves and fish meal; planned and recorded in the experiment |
||||
|
TS25 |
TS50 |
TS75 |
TS100 |
Planned |
25 |
50 |
75 |
100 |
Recorded |
30.6 |
53.4 |
76.6 |
100 |
There were significant differences between treatments for intake of palm syrup and total DM (Table 5).
Table 5.
Mean values for feed and nutrient intake in pigs fed sugar palm
syrup with increasing proportions |
||||||
|
TS25 |
TS50 |
TS75 |
TS100 |
SEM |
P |
DM intake, g/day |
|
|
|
|
|
|
Taro silage |
60.7a |
118b |
208c |
232c |
|
|
Fish meal |
118d |
100c |
46.4b |
0a |
|
|
Sugar palm syrup |
301b |
328b |
327b |
261a |
9.10 |
0.001 |
Total DM |
480a |
546b |
581b |
491a |
15.50 |
0.001 |
DM, g /kg LW |
24.9a |
34.1b |
33.2b |
30.1b |
2.35 |
0.032 |
abcd Mean values within rows with different superscript letters are different at P<0.05 |
The relationship between DM intake and dietary protein from ensiled taro leaves was curvilinear (Figures 1, 2, 3) with maximum intake at about the 75% replacement of fish meal, followed by a decline to the 100% level. The trend for intake of palm syrup was similar. The reason for the decrease in intake of the TS100 diet may have been the "bulkiness" of the diet because of the high content of the low DM silage. The DM intake expressed as a function of live weight on the TS100 diet (30.1 g/kg) was lower than reported by Rodriguez et al (2006) (48.5 g DM/kg live weight) for a similar diet fed to pigs of similar live weight, but with sugar cane juice instead of palm syrup and fresh leaves of Xanthosoma sagittifolium instead of ensiled leaves of Colocasia esculenta.
|
|
Figure 1: Relative intakes of DM from dietary ingredients
(TS taro leaf silage, FM fish meal, SP sugar palm
syrup) |
Figure 2: Relative intakes of crude protein from dietary
ingredients |
|
Figure 3. Relationship between intake of palm syrup and
total DM and proportion of dietary protein from ensiled taro
leaves |
There were no significant differences among treatments in apparent digestibility of DM and organic matter (Table 6) which were high in all cases. The value for DM of 87.7 on the TS100 diet was slightly higher than was reported by Rodriguez et al (2006) for a diet of sugar cane juice and fresh leaves of Xanthosoma sagittifolium (83.4%). If it is assumed that the sugar palm syrup is 100% digested, and as it contributed 53% of the diet DM in treatment TS100, it can be predicted that the apparent digestibility of the taro leaf silage would be 73.8% for the DM and 86% for the organic matter.
Table 6. Mean values for diet digestibility in pigs fed sugar palm syrup with increasing proportions (25 to 100%) of protein from taro leaf silage replacing protein from fish meal |
||||||
Apparent digestibility, % |
TS25 |
TS50 |
TS75 |
TS100 |
SE |
P |
Dry matter |
84.7 |
85.6 |
84.5 |
87.7 |
1.4 |
0.370 |
Crude protein |
75.3ab |
78.1b |
69.4ab |
66.1a |
2.8 |
0.019 |
OM |
89.6 |
91.5 |
88.6 |
93.4 |
2.13 |
0.418 |
ab Mean values within rows with different superscript letters are different at P<0.05 |
Crude protein apparent digestibility differed among treatments (P<0.05) with a negative curvilinear trend (Figure 4), as the proportion of protein from taro silage was increased, with the lowest value of 66.1% on the TS100 diet. A similar negative trend was reported by Rodriguez et al (2006) with a value of 61.4% for the diet with only cane juice and Xanthosoma leaves. These negative effects can be attributed to the binding of some of the proteins to the fibre which reduces its digestibility (Jørgensen et al 1996; Kass et al 1980). Shayo and Uden (1999) reported that 64% of the protein in Xanthosoma leaves was in the NDF fraction; however, a much smaller fraction (21%) was reported by Leterme et al (2005) for leaf protein in Xanthosoma.
|
|
|
Figure 4. Relationship between apparent digestibility of
crude protein and proportion of diet protein from ensiled taro
leaves |
|
Figure 5. Mean values for N balance in pigs fed sugar
palm syrup with increasing proportions of protein from taro leaf
silage replacing protein from fish meal |
There were significant differences in all the components of N balance (Table 7; Figure 5).
Table 7.
Mean values for N balance in
pigs fed sugar palm syrup with increasing proportions of protein
from |
||||||
|
TS25 |
TS50 |
TS75 |
TS100 |
SEM |
P-value |
Components of N balance, g N/day |
||||||
Intake |
10.2a |
12.0b |
13.5c |
10.4a |
0.36 |
0.001 |
Faeces |
2.47a |
2.21b |
3.68a |
3.57a |
0.33 |
0.019 |
Urine |
4.53ab |
5.18a |
4.47ab |
3.82b |
0.33 |
0.053 |
N retained |
|
|
|
|
|
|
g/day |
3.26b |
4.58a |
5.42a |
2.89b |
0.33 |
0.001 |
g/day# |
3.68 |
4.40 |
4.72 |
3.24 |
0.36 |
0.099 |
% of N intake |
34.9 |
38.4 |
38.2 |
27.7 |
3.00 |
0.13 |
% N digested |
43.2 |
49.1 |
53.1 |
39.6 |
3.80 |
0.42 |
# Adjusted
for differences in N intake by using
covariate analysis |
Faecal N tended to increase (P<0.05) and urine N to decrease as the proportion of taro leaf silage increased. Similar trends were reported by Rodriguez et al (2006) for diets of sugar cane juice and Xanthosoma leaves. There were significant effects of N intake on N retention (P<0.001), but not on N retention as % of intake and % of digested N (P>0.05). The responses to increasing intake of dietary taro leaf protein were curvilinear for N retention (adjusted for N intake; Figure 6) and for N retained as % of N intake and as % of digested N (Figure 7).
|
|
|
|
Figure 6. Relationship between N retention (adjusted for
N intake) and proportion of diet protein from ensiled taro
leaves |
|
Figure 7. Relationship between N retention as % of intake
and % of digested N, and proportion of diet protein from ensiled
taro leaves |
This response followed closely the trend for DM intake (Figure 1) implying that the best results would be with 75% replacement of the fish meal by the taro leaf silage. The similar values for N retention on TS0 (all fish meal) and TS100 (all taro silage) suggests that the amino balance was not a limiting factor to pig performance. This is supported by the conclusion of Leterme et al (2005) that "tropical tree leaves offer a variable amount (170-240 g kg−1) of proteins that are well balanced in essential amino acids but not well digested by pigs".
The N retention values in general were lower (range 2.9 to 5.4 g
N/day) than those recorded by Rodriguez et al (2006) (range 6.1 to
9.7 g N/day). The main reason for this would seem to be the lower
DM intake (25 to 34 g DM/kg LW) compared with the experiment of
Rodriguez et al (2006) (49 to 56 g DM/kg LW). The diets were
similar in overall composition (mainly sugars as the energy
component and leaves of similar plants species (Old Cocoyam versus
New Cocoyam)). The difference in response in feed intake could be
due to the previous feeding history of the two sources of pigs.
These were of similar live weight (15 kg in this study versus 13.4
kg in the experiment of Rodriguez et al (2006)). However, the pigs
in the latter study were from sows that had been fed leaves of New
Cocoyam during pregnancy and lactation, when the piglets also had
access to the leaves. Tien and Preston (2003) concluded that
"reductions in growth rate at weaning time when piglets are first
offered solid foods, or subsequently due to frequent changes in
diet, can be reduced if novel foods are eaten pre-natally by mother
or post-natally by mother and piglets together".
There were positive curvilinear trends in DM and crude protein intake and in N retention in response to replacement of fish meal by ensiled taro leaves with the optimum proportion being at about 70-75% replacement.
Coefficients of DM apparent digestibility were high on all diets but those for crude protein showed a negative curvilinear response with declining values beyond 25% substitution of the fish meal protein by that from taro leaf silage.
The limiting factor to utilization of the taro leaf silage
appears to be the lower apparent digestibility of the protein in
the taro leaves and maybe amino acid imbalance of the protein, or a
greater proportion of crude protein fermented in the
caecum.
The present experiment is part of a study on ensiled taro
(Colocasia esculenta) leaves in diet of local
crossbred pigs in Cambodia, supported by the MEKARN project
financed by SIDA-SAREC. The authors express their gratitude to all
the personal of the CelAgrid Ecological Farm, for help with the
experiment. This paper forms part of the MSc thesis (MEKARN-SLU,
Uppsala, May 2007) of the senior author.
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