Use of Cassava as Animal Feed |
Two
experiments were carried out to determine the effect on silage quality, and on
feed intake and digestibility by growing heifers, of including molasses in
cassava tops silage. Four levels of sugar cane molasses: (0, 30, 60 and 90 kg
per tonne of fresh cassava tops) and two storage periods (30 and 60 days) were
compared.. The design was a 4*2 factorial completely randomized block design
with 3 replicates. For the feed intake and digestibility study, the silage was
made without or with 60 kg molasses/tonne, using sixteen plastic bags of 1m
diameter. Six crossbred Holstein heifers, of 160 - 180 kg live weight, were
randomly allocated in a 3 x 2 change-over design to three treatments: Guinea
grass ad libitum, 70% of the ad
libitum grass intake with a supplement of non-molasses cassava silage ad libitum, and 70% of the ad libitum grass intake with a
supplement of molasses cassava silage ad
libitum.
Based on the colour, smell and mould appearance, all the silages
were considered to be acceptable, but with higher levels of spoilage with the
highest level of molasses. The silage made with molasses had a lower pH but a
similar concentration of lactic acid compared with the silage without molasses.
Ensiling reduced the HCN and tannin contents of the cassava tops.
The voluntary feed intake per
100 kg live weight of the heifers was 2.59, 2.65 and 2.91 kg DM of Guinea
grass, non-molasses cassava tops silage and the molasses cassava tops silage
diet, respectively. The apparent digestibility of DM, OM, CP, NDF and ADF
decreased in the silage supplemented diets. No significant difference in
digestibility was found between the non-molasses and molasses silage diets. The
digestibility coefficient (%) of DM, OM, CP, NDF, ADF in non-molasses cassava
tops silage and molasses cassava tops silage was 49.4, 52.1, 45.81, 36.6, 27.7
and 49.7, 51.9, 47.55, 28.1, 19.5, respectively.
It is concluded that cassava
tops can be preserved successfully by ensiling with or without molasses
additive and that cassava tops silage is a good feed resource for cattle.
Cassava or tapioca (Manihot esculenta, Crantz) is an annual
crop grown widely in the tropical regions of Africa, Asia and Latin America. It
thrives in sandy-loam soils with low organic matter, and climates characterized
by low rainfall and high temperature (Wanapat et al 1997). In Vietnam cassava
is cultivated on an area of 231,700 ha (FAOSTAT 1998). It is the third food
crop after rice and maize and is mainly cultivated by small-holder farmers in
the poorer areas. The main product of cassava is the roots, but considerable
quantities of green leaves remain attached to the stem when the roots are
harvested. Ravindran and Rajaguru (1988) reported the yield of cassava leaves
to be as much as 4.6 tonnes/ha of dry matter taken as a by-product at root
harvesting. High contents of crude protein in the cassava leaf have been
reported, varying from 17 to 40% in the dry matter (Allen 1984). FAO (1998) reported that with practices
directed only toward harvesting of foliage, up to 6 tonnes of crude protein can
be obtained per hectare per year. In Vietnam, cassava leaf residues have been
evaluated by Liem et al (1998) in several experiments with monogastric animals.
Focussing on the root production, many new high yielding varieties of cassava
have been introduced, of which several have a high HCN content in the leaves
(Kim 1999). HCN toxicity is considered to be a limiting factor in using a high
level of cassava leaves in the diets of monogastric animals. However, ruminants
can neutralize the harmful effects of HCN through the activities of rumen
microbes and can therefore utilize the leaves more efficiently. In the FAO
Tropical Feeds database (FAO 1998), it is stated that cassava leaf meal can be
mixed in concentrates for lactating cows at up 35% without any harmful effects.
Hay made from cassava
leaf and stem was shown to be a good feed resource for ruminants, with a high
voluntary feed intake (3.1% of LW) and dry matter digestibility (71%) (Wanapat
et al 1997). However, to produce good quality hay from cassava tops requires
good weather for drying and special care must be taken to limit the loss of dry leaves. Ensiling
could be a suitable way of preserving the leaves but silage additives should be
added to ensure successful fermentation when the ensiled material, such as
cassava tops, has a high content of nitrogen and low concentration of water soluble
carbohydrates (Petersson 1988). Sugar cane molasses, a common feed ingredient
in the tropics, is frequently used as an additive for ensiling tropical forages
and improving silage quality.
The present study was therefore aimed at
determining the influence of molasses in making silage from cassava tops and
evaluating the feed intake and digestibility when the silage was fed to growing
crossbred Holstein heifers.
Four levels of
sugarcane molasses (0, 30, 60 and 90 kg per tonne of fresh cassava foliage),
and two storage periods (2 and 4 months) were evaluated according to a 4*2
factorial randomized complete block design with 3 replicates. A total of 24
plastic bags with 10 kg each of fresh cassava foliage were prepared. Cassava
tops were collected in the field immediately after root harvesting in January
1999. Only the tops (leaves, petioles and 40-60 cm of green stem) were taken.
The molasses contained 640 g dry matter and 375 g sugars per kg. The tops were
chopped into pieces that were 3 to 4 cm
in length. The chopped material was mixed with the molasses and placed
in the plastic bags. The contents of the bags were compacted by hand, bound
with a string and pressed by placing one sand bag (2 kg) on top of each bag.
Samples were collected
for chemical analysis on two occasions, two and four months after ensiling. The
characteristics of the silages; colour, fungal contamination and smell were
evaluated. Determinations were made of toluene dry matter (dried and corrected
for volatiles according to Lingvall and Ericson 1981), pH (pH-ORION model 420
A), water soluble carbohydrates (WSC), tannins, HCN, N, ash, and EE using the
procedures described by AOAC (1984). ADF and ash-free NDF were analyzed
according to Van Soest and Robertson (1980). Acetic, butyric and lactic acids
were determined by the HPLC technique (Shimadzu, Japan 3081-09202-20ATD-E).
Approximately 4000 kg of cassava
top residues were collected in the field immediately after root harvesting in
February, 1999. Sixteen plastic bags (1.0 m diameter), containing about 260 kg
of chopped cassava tops each, were used to make the silages. The cassava tops
were chopped into pieces 3 to 4 cm in length and placed in plastic bags in
layers of 1.0 - 1.4 m deep. Molasses was mixed with the chopped material at the
time of filling and the mixed materials were compacted by two people standing
in the bags. After filling, the tops of the bags were bound by plastic string
and pressed by placing five 8 kg sand bags on top. After 4 months of storage,
the silage was used in the intake and digestibility experiment.
Six crossbred Holstein heifers, 8-10 months of age and 160-180 kg live weight, were randomly allocated in a 3*2 change-over design (Patterson and Lucas 1962) to three treatments:
Each period included 14 days for
adaptation, 5 days for measurement of feed intake, 2 more days adaptation and 7
days for digestibility measurement. At
the beginning of the experiment a 5-day preliminary testing was done to
measure the voluntary dry matter intake of the grass diet by each animal in
order to determine the ratio of cassava top silage in the experimental diets
(planned to be 70: 30 grass: silage on dry matter basis). During the feed intake measurement the grass
supply on the treatments 0MS and 6MS was restricted to 70% of the ad libitum intake (on a DM basis) and
cassava silage was supplied ad libitum.
For the digestibility determinations the total diet was limited to 85% of the
mean DM intake measured during the 5 days of intake studies. During the 9 days
of the digestibility study the daily amount of feed was maintained constant.
The animals were confined in individual stalls in a covered shed open at the sides. They were kept for one month in this location prior to starting the experiment in order to adapt them to the experimental conditions. They were treated against internal and external parasites. During the experiment the animals were fed 4 times per day: at 8:30, 11:00, 16:00 and 20:00 h. Fresh Guinea grass (Panicum maximum 280), cut at six weeks of re-growth was used as the basal feed. Cassava tops silage with or without the molasses additive was taken from the plastic bags once per day, weighed and put into a small plastic bag for feeding the whole day. A mineral supplement (containing salt, dicalcium phosphate, MgSO4, CuSO4, CoCl2, K2SO4, Casein Iodine, MnSO4 and Selenium) was fed at 84g/150-200kg live weight /day. Water was freely available.
The animals were weighed prior to and after the 5-day feed intake period in the morning, before feeding and watering. The mean weight of the heifer was used in calculating the feed intake per kg live weight. Samples of feeds offered and refused were collected every day for laboratory analysis. During the collection period, refusals were collected at 8:00 h, weighed, mixed, sub-sampled and bulked in bags, one for each animal. During the digestibility study, feces from each animal were collected immediately after defecation throughout the day, and placed in weighed plastic basins until 8:30 h the following morning. The 24-hour fecal output was weighed, mixed and a sub-sample (10% of the daily output) from each individual heifer was stored in a freezer (-20 ºC). The seven samples from each animal during the collection week were de-frosted, mixed, sampled and dried in a forced oven at 60oC for 72 hours for laboratory analysis. Samples were prepared using procedures described by Goering and Van Soest (1970). Feed, refusals and feces samples after oven drying were ground using a laboratory hammer mill with 1mm screen. Dry matter, ash, crude protein, ether extract, ADF, ash-free NDF and permanganate lignin were analyzed using the same methods as described in the ensiling study. Gross energy contents of feed and fecal samples were determined by means of an adiabatic bomb calorimeter and digestible energy was calculated from these results.
The data were subjected to an analysis of variance (ANOVA)
by using the General Linear Model (GLM) procedure of Minitab (1998). When the F
test was significant (P<0.05), Tukey’s test for paired comparisons was used
(Minitab 1998).
Observations
at 2 and 4 months after ensiling (Table 1) showed that the silage colour was
pale green to brown yellow at 2 months after ensiling and changed to a yellow
to brown colour after 4 months of storage. The molasses additive increased the
degree of brown colour in the silage. Moulds were not seen 2 months after
ensiling, but increased with the amount
of molasses additive and the time of
storage. The smell was good for all treatments. Based on the colour, smell and
mould appearance, the silages were considered to be acceptable without or with
the low level of molasses additive for the shorter storage period, and to be
acceptable, but with a proportion spoiled after the long-term storage and with
the high level of molasses additive.
Table 1. Classification of cassava tops silage
with different amounts of molasses additive and 2 or 4 months storage |
||||||||
|
Molasses level |
|||||||
|
0% |
3% |
6% |
9% |
||||
Storage
mae |
2 |
4 |
2 |
4 |
2 |
4 |
2 |
4 |
Colour |
Gy |
Yb |
Gy |
Yb |
By |
Yb |
By |
Yb |
Moulds |
Abs |
Ot1-2 |
Abs |
Ot1-2 |
Abs |
Ot3-4 |
Abs |
Ot3-4 |
Acceptable |
A |
A |
A |
A |
A |
A +sp |
A |
A +sp |
mae:
Months after ensiling. Gy:
Greenish yellow; Yb: yellowish brown; By: browish yellow; Pg: Pale green; Abs:
absent; Ot+number: only on top with cm in thickness A:
Acceptable; A+sp: Acceptable with spoiled portions; |
The dry matter of the fresh cassava was 25.8% and only small changes were noted during
ensiling on all treatments (Table 2). There were trends towards increased DM
content at higher levels of molasses, and to reduced DM content with storage
time. The crude protein content of the
cassava tops was around 21% of DM , and in the non-additive silages did
not change after ensiling. As was to be
expected, incorporation of molasses (contains less than 4% crude protein in dry
matter) in the silage led to reduced
crude protein content, especially at
the higher levels of molasses added. Storage time reduced the crude
protein of the silage somewhat, but the
changes were non-significant. The NDF concentration was decreased 8% after
ensiling for the cassava tops silage without added molasses. The NDF content
was reduced with storage time.
Table 2a. The effect of molasses and storage period on the
quality of cassava top silage (g/kg DM except for DM content which is on
fresh basis) |
|||||||
|
pH |
DM |
CP |
EE |
NDF |
ADF |
Ash |
Fresh tops
|
|
258 |
21.1 |
10.4 |
56.1 |
37.0 |
6.76 |
Silage (molasses level) |
|||||||
0 |
4.39 |
267 |
21.6a |
11.8 |
51.4 |
37.1 |
7.21 |
30 |
4.21 |
266 |
19.8ab |
12.5 |
47.4 |
37.0 |
6.72 |
60 |
4.29 |
274 |
19.3b |
13.6 |
45.8 |
38.4 |
7.04 |
90 |
4.28 |
277 |
18.2b |
12.6 |
47.3 |
37.0 |
6.71 |
Probability |
0.10 |
0.41 |
0.00 |
0.26 |
0.09 |
0.77 |
0.64 |
Storage time
|
|
|
|
|
|
||
2 months |
4.38a |
280 |
19.9 |
12.5 |
37.3 |
|
6.62 |
4 months |
4.21b |
264 |
19.5 |
13.8 |
46.0b |
37.4 |
7.22 |
Probability
|
0.01 |
0.08 |
0.32 |
0.66 |
0.02 |
0.94 |
0.10 |
Table 2b. The effect of molasses and storage period on the
quality of cassava top silage (mg/100g DM) |
|||||||
|
A. lactic |
A. acetic |
WSC |
Tannin |
HCN |
||
Fresh tops |
|
|
6.34 |
3.83 |
97.7 |
||
Silage (molasses level) |
|
|
|||||
0 |
0.97 |
0.23 |
0.65a |
2.87 |
28.1 |
||
30 |
0.95 |
0.24 |
1.16b |
2.84 |
27.1 |
||
60 |
0.99 |
0.23 |
1.44c |
3.07 |
27.1 |
||
90 |
0.99 |
0.23 |
1.35c |
2.66 |
26.5 |
||
Probability |
0.13 |
0.36 |
0.00 |
0.95 |
0.77 |
||
Storage time |
|
|
|||||
2 months |
0.96 |
0.23 |
1.14 |
2.83 |
30.9a |
||
4 months |
0.99 |
0.24 |
1.16 |
2.89 |
23.5b |
||
Probability |
0.06 |
0.13 |
0.10 |
0.89 |
0.00 |
||
The mean pH value of the non-molasses silages was 4.39. The molasses additive tended to decreased pH, while storage time significantly decreased the pH. The mean lactic acid content was around 1% of DM, and no effects of molasses additive level and storage period were found. Butyric acid was not detected in any of the silages. Water soluble carbohydrates increased in the silages made with molasses but were reduced by 90 % in the absence of molasses.
The HCN content in the fresh cassava tops was 98 mg per 100g
DM and was reduced by 68 % after 2
months of ensiling. Increasing the storage period reduced the HCN level but the
molasses additive had no obvious effect. The tannin content of the cassava tops
was reduced after ensiling, but the decrease was small, and no significant
change was found due to storage time. There was no apparent effect of the
molasses on the silage tannin content.
Intake of dry matter was highest for the treatment with 6%
molasses added to the silage (Table 3) but organic matter digestibility organic
matter digestibility (OMD) and crude protein digestibility (CPD) of the silage
diets by around 5 and 10 percentage units, respectively, as compared to the
grass diet only. There was no difference in OMD and CPD between the 0MS and
6%MS diets. The digestibility of the fiber fractions in the diets, expressed as
NDF digestibility (NDFD) and ADF digestibility (ADFD), were also significantly
lower in the cassava tops silage diets. The differences were 7 – 11 percentage
units for NDFD and 11 – 14 percent units for ADF. No significant difference
could be found between the 0MS and 6%MS diets. The energy digestibility (ED) of
the silage supplement diets was also lower by around 5 percent units compared
to the grass diet.
Table 3. Daily
dry matter feed intake |
||||
|
Guinea grass, |
Silage supplemented
diets, |
Probability |
|
0% Molasses |
6% Molasses |
|||
Feed (kg DM / animal) |
||||
Grass |
5.29 a |
3.37 b |
3.34 b |
0.001 |
Silage |
0.00 a |
2.06 b |
2.39 b |
0.001 |
Total |
5.29 |
5.43 |
5.73 |
0.80 |
ab Means within rows
with different superscript letters are
different (p<0.05). |
Replacing Guinea grass with ensiled cassava tops depressed
digestibility of most fractions (Table 4).
Table 4.
Digestibility (%) of the grass and silage supplement diets and the
cassava top silages assuming constant digestibility of Guinea grass |
|||||||
Apparent digestibility |
Guinea grass |
Silage diets |
Prob. |
Cassava top silage |
Prob |
||
0 % Mol |
6% Mol |
0% Mol |
6% Mol |
||||
Dry matter |
61.6 a |
57.0 b |
56.6 b |
0.001 |
49.3 b |
49.6 b |
0.001 |
Organic matter |
64.5 |
59.9 b |
59.1 b |
0.001 |
52.1 b |
51.8 b |
0.001 |
Crude protein |
63.2 a a |
53.0 b |
53.1 b |
0.001 |
45.8 b |
47.5 b |
0.001 |
Ether extract |
62.5 |
56.5 |
53.4 |
0.15 |
53.6 |
49.4 |
0.09 |
Ash |
22.5 |
18.9 |
20.6 |
0.10 |
20.9 |
24.3 |
0.33 |
ADF |
60.1 a |
48.7 b |
45.5 b |
0.001 |
27.6 b |
19.4 b |
0.001 |
NDF |
66.2 a |
59.2 b |
55.1 b |
0.001 |
36.5 b |
28.1 c |
0.001 |
Energy |
62.6 |
57.6 |
56.9 |
0.08 |
50.3 |
51.5 |
0.28 |
abc Means within rows
with differing superscript letters are different (P<0.05) |
With DM content between 25 and 35% and pH values below 4.5
the silage quality could be considered to be good (Pettersson 1988). The molasses and storage reduced pH values.
Butyric acid is another quality parameter, and silage is considered to be good
when the concentration is below 0.1 g/kg fresh material (Lättemäe
1997). No butyric acid was detected in any of the silage samples. The presence
of mould in silage is undesirable because it uses silage nutrients and toxins
are sometimes produced . There were increasing problems with moulds and spoiled
portions with increasing amount of molasses and longer storage period.
The WSC in herbage is the main substrate for microbial
growth. Therefore, concentration of WSC is reduced during fermentation. More
variable results were obtained in residual WSC at increased levels of molasses,
probably because part of the added sugars was lost in the effluent. It was
expected that a higher dose of molasses should result in a higher residual WSC
and improve silage quality, as reported
by Lättemäe et al (1997), but in our study high levels of molasses resulted in more molasses in the run-off.
Haigh and Parker (1985) suggested that a critical WSC concentration in herbage
for successful preservation as silage without additives is 30 g/kg DM. In legumes, Zelter (1960) suggested a
higher WSC level of 120g/kg DM because of low dry matter content at harvest. In
our study the WSC content of cassava tops was in the middle of the range
reported by these two authors.
Non-additive silage had nearly the same lactic acid
concentration compared to the additive silage treatments, suggesting that WSC
was not the sole substrate for lactic acid bacteria Starch, the main storage
carbohydrate in leaf and stem, may be a substrate after the attack of enzymes
in the initial ensiling process, although the majority of lactic acid bacteria
do not attack starch (McDonald et al
1991). However, the lactic acid
concentration, which was in the range of some common tropical herbage silages
(Aminah et al 1999), was still low compared to the values for temperate legume
silage (Lättemäe et al1997).
The reduction in HCN content in cassava is due to the action
of endogenous linamarase on glucosides following loss of cell integrity or
tissue damage. In the ensiling process, chopping and slight wilting during the
preparation before sampling, pressing and the initial environment of the
aerobic phase resulted in good conditions for reducing the HCN content. When
the pH in silage is lowered the enzyme activities are restricted, and the speed
of HCN elimination reduced. In this experiment the HCN content of the cassava
tops silage was reduced with storage time, but no effect was found of additive
level. Similar results were found by Du
Thanh Hang (1998) and Bui Nhu Phuc et al (2000) for cassava leaf silage.
The tannin content of the silage materials was in the range
of common tropical high-protein leaves (Mahyuddin et al 1988; Ahn et al
1989), and was reduced in the initial
period of ensiling. This reduction may have been due to the formation of
tannin-protein complexes. Maldonado
et al (1995) reported that insoluble tannin and plant leaf protein
complexes were established in the pH range 3.5-5.5. In ensiling sorghum with
different tannin contents, Rodrigues et al (1998) reported that tannin
concentration decreased with increase in the duration of fermentation. No
such reduction with the time of storage
and level of molasses additive was found in the present study.
Supplementing cassava top silage to the grass diet tended to increase the feed intake, which could have been a result of a stimulatory effect of silage on intake (Aminah et al 1999), or the effect of the protein in the cassava leaves when added to a low-protein roughage diet (Merkel et al 1999). In the present study, the supplement increased the crude protein intake by 45 to 63% compared with the grass diet. Molasses addition also improved silage quality, which would also result in a higher feed intake (10%) compared with non additive silage. Similar results have been reported by other authors (Pettersson 1988; Lättemäe 1997).
Using
cassava tops hay as the sole feed Wanapat et al (1997) found a DM digestibility
of 71%, which is much higher than the value in the present study (50%).
Treatment method may explain some of
the difference as water soluble components may be lost in the run-off.
In one study Clancy et al (1977) reported that making alfalfa hay by drying can
improve the digestibility by 7% compared with silage making. In the present study,
digestibility of the cassava silage was determined by difference and the actual
result for cassava may not be the same when used as a supplement compared with
being the sole feed, as found by Madrid et al (1997).
Financial support from SIDA-SAREC is gratefully
acknowledged. The authors would also like to thank Ms.Tran Thi Phuong Dung of
the UAF Animal Nutrition Department for help in the analyses, and Mr. Nguyen
Van Hiep for help with the field work.
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