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| Improvement
of cattle production systems for productivity
enhancement
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C . Devendra |
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(Consulting
Animal Production Systems Specialist, 130A Jalan
Awan Jawa,
58200 Kuala Lumpur, Malaysia).
In
the search for efficiency in the use of natural
resources, productivity enhancement assumes that
there will be maximum use of the available animal
genetic resources. In this context, it is imperative
to ensure that the available cattle breeds are fully
used to the extent possible. Among the non-genetic
factors, the significance of feeding and nutrition
on the potential performance of indigenous cattle
is discussed with reference to knowledge of the
availability and value of feeds, effective use in
feeding systems that can promote higher performance
and contributions to food, draught and manure production.
These benefits are important for improved livelihoods
and sustainable development. The adaptation and
physiological traits peculiar to indigenous cattle
are summarised. Key features in these cattle are
ability to cope with stresses due to feed unavailability,
droughts, and ability to recover much faster from
these problems. Data on growth performance and effects
of supplementation are reviewed. Supplementation
is especially important to ensure high performance
in cattle, and is reflected in reports from several
countries, to include both multi-nutrient and mineral
sources and leguminous forages. Economic justification
for supplementation is critical and is illustrated
from data on beef production based on feeding ammonia
treated straw and cotton seed cake in China. The
potential of indigenous breeds is also highlighted
in several studies that demonstrated large differences
comparing cattle reared in traditional and improved
systems. Opportunities for increased contribution
from cattle are indicated.
Key
words: Cattle, breeds, production
systems, feeding and nutrition, improvement
productivity enhancement , conservation.
1.
Introduction : The justification
of maximizing productivity from the available cattle
genetic resources in directly associated with the
fact that the demand for foods of animal origin
is way in excess of current supplies, due to population
growth, urbanisation, increased disposable income
and changing consumer preferences. The situation
is especially awesome in Asia where there exists,
the largest demands for foods of animal origin,
namely meat and milk. These factors place unprecedented
pressures on the use of natural resources and re-emphasise
efficiency in their use that are consistent with
maximizing productivity
It is therefore imperative to make the best use
of the available indigenous cattle breeds to the
extent possible. India has a unique and enviable
cattle genetic diversity. The breeds are widely
found and distributed to the various agro-ecological
zones to which they are fully adapted. Very good
examples of some outstanding breeds are Yellow cattle
of China and Vietnam; Gir, Sahiwal and Tharparkar
dairy breeds, and Kangayam, Krishna Valley and Ongloe
breeds used for draught in India; Bali and Madura
breeds in Indonesia, Kedah-Kelantan or Kedah-Thai
breed in Malaysia and Thailand ; Red Sindhi from
Pakistan. The adaptation to the environment involves
several important attributes, both anatomical and
physiological which then enables them to express
multi-purpose function. These include production
of meat, milk, draught power and haulage, and also
dung. Table 1 presents the range of products and
services from cattle.
It is not fully known about the extent of the adaptive
qualities and also potential productive capacity
of many of these indigenous cattle breeds. A first
essential therefore is establishing full understanding
of their attributes and capacity in their environment
of origin in order to get the best from these cattle.
Beyond this, further improvements can be considered
as appropriate.These considerations must also involve
the need for conservation.
This paper is concerned with the potential improvements
to productivity enhancement in cattle. It emphasises
the importance of giving attention to non-genetic
factors in which improved feeding and management
is an important means to ensure maximum productivity
and the potentiality of indigenous cattle. It draws
attention to the importance and peculiarities of
these cattle in farming systems.
Table
1. Cattle products and services in Asia :
| Products |
Services |
Meat
( raw, cooked, blood, soup)
Milk (fresh, sour, yoghurt, butter, cheeses,
ice cream, baby foods )
Skins (clothes, shoes, water/grain containers,
tents, handicraft, thongs etc.)
HornsBones ( handicraft )Manure and urine (crops,
fish) |
Cash income
and investment Security and insurancePrestige
in ownershipGifts and loansReligious rituals
eg. sacrificial
slaughter Human nutrition – beneficial
characteristics of meat and milkPack transport
and draught powerDraught powerMedicine |
2.
The search for efficiency : In
the search for efficiency in the use of animal genetic
resources, it is especially important therefore that
in most situations to take cognisance of the following
issues (Devendra, 1999):-
· Full knowledge of the availability and potential
value of the available feed resources
· Effective use in feeding systems that gives
predictable levels of performance.
· Identification of the objectives clearly
in terms of production and profitability, and
· Ensuring that the resulting benefits are
consistent with sustainable development and environmental
integrity.
Associated with above and viewed from a farming systems
perspective, it is also imperative to consider the
following interrelated issues:
· Knowledge of the totality of feeds (forages,
crop residues, agro-industrial by-products, and non-conventional
feeds).
· Consideration of their nutrient composition
and digestibility.
· Appropriateness and efficiency of use within
production systems
· Cost of feeding as percentage of total production
costs, which account for about 50-60% in ruminants
(meat and dairy), and 65-80% in non-ruminants (meat
and eggs) in intensive production systems, and
· Self-reliance in the efficient use of feeds.
3. Adaptation and physiological
traits : It
is pertinent to keep in perspective, the adaptation
and physiological traits that are peculiar to indigenous
cattle. In order to focus on peculiarities more closely,
the differences in the arid and semi-arid, and wet
zones are identified. Table 2 summarises the situation,
adapted from data that have been reported previously
(Devendra, 1987):-
Table 2. Adaptation and physiological
traits in indigenous cattle.
Trait |
Arid/semi-arid
zone |
Sub-humid
/ humid zone |
| Size
and morphology |
·
Taller
· Larger size (350-450 kg)
· Loose skin and appendages
· Able to walk long distance |
·
Shorter, compact body
· Medium size (300-500 kg)
· Higher hair density
· Coarse pigmentation
· More sweat glands
· (800-1500/cm2 ) |
| Heat loss |
·
Panting
· Sweating
· Cooling |
·
Reduced panting
· Sweating
· Cooling |
| Feeding
behaviour and metabolism |
·
Relatively lower feed intake
· Grazer (3-5 km/day)
· More active
· Walk long distance
· Dietary N in less well digested |
·
Relatively higher feed intake
· Utilise forages efficiently
· With coarse roughages
· longer retention time |
| Dry season
feed stress |
· Better ability to
cope with the problem
· Recovery is much faster |
·
Less stress due to more feed availability |
| Water economy
and turnover rate |
·
Water turnover rate higher than buffaloes
· Higher urine concentration
· Evaporative water
· Loss comparable to sheep |
·
Less evaporative
· Water loss due to humidity
· Normal urine concentration |
Table 1 indicates
that the adaptation and behavioural responses by indigenous
cattle are different in the arid and semi-arid zone
compared to the wet tropics. With feeding and nutrition
for example, cattle are able to walk relatively long
distances in search of feeds in the arid areas. Forages
are generally well utilised, however, there exists
differences in the rate of passage and retention time.
Warren et al. (1974) showed that the retention time
of steers fed forage diets increased when the environmental
temperature increased from 18 to 32oC with associated
increased digestibility of dry matter, cellulose,
acid detergent fiber and neutral detergent fiber.
It is not clear if thermal stress affects all parts
of the digestive tract, but it is likely that physical
form of the diet is implicated in the rate of passage
of digestion.
One of the other
characteristics of indigenous cattle is their distinctive
ability to recover quickly from period of feed shortages
or droughts. This is a very vivid situation in India.
In Australia, Moran (1973) found that buffaloes and
Brahman crosses grew equally well over 15 months on
improved tropical pastures and at twice the rate of
bantengs and Shorthorns. However, during the dry season,
live weight losses were smaller in the bantengs and
buffaloes than in the Shorthorns or Brahmans. The
ability of the banteng to maintain body condition
and perform better on poor quality pastures has also
been noted in other countries such as Thailand and
Pakistan. Such observations could be partly due to
species differences in voluntary feed intake and utilisation
of low quality dry season roughages. These observations
implicate that these might partly be due to species
differences in voluntary feed intake and utilisation
of low quality roughages such as cereal straws and
feeds in the dry season. However, the results of Moran,
Norton and Nolan (1979) indicate that there are few
differences between cattle species in their ability
to digest and utilise low quality roughage when comparisons
are made between animals of similar live weight and
feed intake. The same authors have also reported that
with the exception of the Shorthorn, there was little
difference in diet digestibility on gross nitrogen
and phosphorus metabolism when all animals were fed
on low quality roughage at the same intake relative
to body weight.
Associated with
these adaptation and physiological traits, it is also
important to keep in perspective that these indigenous
cattle are multi-purpose animals kept for a variety
of reasons other than food production. These include
value as assets and security, insurance, draught,
manure production and recreation. The last three contributions
are underestimated in most countries
and it is important to emphasise that these drought
and use of manure are especially significant for crop-animal
systems without which these systems are likely to
collapse (Devendra, 2000b). Considered together, indigenous
cattle in the tropics are extremely valuable for a
number of reasons, and their potential importance
is associated with three important features:
1. Individual breeds
are fully adapted to local environments in which they
are especially productive, namely low input and sustainable
production systems. They have lower feed requirements
and intake and can withstand periods of feed shortages.
2. They provide the bulk of the local beef supplies
and some milk, draught and manure for fertiliser mainly
for smallholder production systems.
3. These breeds are valuable sources of genetic material
which provide for producing improved breeds through
crossbreeding programmes when these are considered
necessary.
4.
Siginificance of efficient feeding and management:
Efficient feeding
and nutrition represents in many situations, the
most important constraint affecting productivity
from ruminants in South Esat Asia and South Asia
(Devendra et al., 1997; Devendra et al., 2000).
Attention to this factor is therefore an important
means to ensure maximum performance in cattle. The
type of response to improved feeding and management
largely depends on diet quality, given observed
interactions between genotype and diet in both feed
intake and live weight change (Moran, 1985). The
difference maybe due to differences in stage of
maturity and hence tissue composition of live weight
gain, but the overriding significance of nutrition
on animal performance is unquestionable.
i)
Growth performance:
Diets containing
85% (high concentrate) and 30% (high roughage) concentrates
were fed to young Madura, Ongole, Bali, Grati (
or Friesian crossbreds) and buffalo bulls in two
separate trials. Growth rates in decreasing order
were Grati, Ongole, Buffalo, Bali and Madura. Genotype
differences were the result of variations in intake
rather than efficiency of feed use. In the high
concentrate diet, the genotypes approached maturity
at different rates, with the Grati at 640 kg and
the buffalo at 420 kg in active growth phases, whereas
the Ongole at 520 kg and Madura at 440 kg were closer
to mature live weights. In the high roughage diet,
genotype differences were in stage of maturity was
less because of their lower live weight at the end
of the shorter feeding period.
There were no differences between species in nitrogen,
phosphorus and calcium balances fed the high roughage
diet were reflected in differences in intake (Moran,
1985). Table 3 presents the performance data recorded
over 112 days in the trials.
Table
3. Performance data recorded during period A of
trial I (154 days) and II (112 days).
(Moran, 1985).
Item |
Trial |
Mandura |
Ongole |
Bali |
Grati |
Buffalo |
Significant
factorsA |
s.d.B |
Midweight
(kg) |
I
II |
324c
290b |
395b
335a |
335c
- |
425a
327a |
320c
314ab |
G,
T
G x T |
|
| Daily
dry matter intake (kg/animal) |
I
II |
5.53c
6.15b |
6.50b
6.50ab |
6.02bc
- |
7.97a
7.08a |
5.80bc
6.61ab |
G |
0×82 |
| Daily dry
matter intakeper unit metabolic live weight
(g kg0.75) |
I
II |
72.6b
87.6ab |
73.3b
82.8b |
76.8b
- |
84.9a
92.1a |
76.9ab
89.5ab |
G,
T |
8×7 |
| Average
daily gain(kg per animal) |
I
II |
0.59c
0.55b |
0.81ab
0.65ab |
0.66bc
- |
0.90a
0.78a |
0.73ab
0.59b |
G,
T |
0×19 |
Feed
conversion ratio(kg dry matter/gain) |
I
II |
9.8a
11.6a |
8.2a
10.3a |
9.7a
- |
9.3a
9.5a |
8.2a
11.7a |
T |
2×7 |
A
Significant factors: G, genotype; T, trial.
B s.d., standard deviation equals the square
root of the error mean square in analyses of variance.
Values in the same line with a common superscript
do not differ (P < 0.05)
(ii) Supplementation
:
Associated with
growth performance, many more studies have been
undertaken on the effects of supplementation. One
of the earliest studies that have been undertaken
were on the Ongole fed with Imperata cylindrica
supplemented with maize or cassava at 3% of metabolic
weight. There were no treatment effects, including
supplementing with urea. They suggested that energy
rather than nitrogen limited the use of I. cylindrica.
Also in Indonesia, a series of studies have been
reported on the effects of supplementing five levels
of rice bran (0, 1-2, 2-4, 3-6 and 4-8 kg/head/days)
to Ongole and buffalo bulls, since this by-product
is commonly available and is widely used by framers.
Feeding rice bran stimulated appetite, initially
improved feed conversion efficiency and increased
growth rates. Each additional kg of rice bran fed
depressed Pennisetum purpureum intake by 0.8 kg
in buffaloes and 0.6 kg in Ongole. Nitrogen and
phosphorus status were improved in the supplemented
animals. It was also concluded that the energy requirements
for maintenance and growth did not significantly
differ between Ongoles and buffaloes and were similar
to values calculated for British cattle (Moran,
1983a). Table 4 summarises the main results.
Table
4. Live weights (on day 80), feed intakes and feed
conversion ratios recorded over 161 days growth
(Moran, 1983a).
Item |
Animal
Species |
Rice
bran supplement (kg/head) |
Effect
of diet |
S.D. |
0 |
1.2 |
2.4 |
3.6 |
4.8 |
| Live weight
(kg) |
Ongole
Buffalo |
305
301 |
313
317 |
316
320 |
319
308 |
332
328 |
NS |
33 |
| Rice bran
dry matter intake (kg/head/day) |
Ongole
Buffalo |
0
0 |
1.05
1.02 |
2.09
2.10 |
3.14
3.01 |
4.04
4.02 |
- |
- |
| Dry matter
intake per unit metabolic body weight (g/kg0×75/day) |
Ongole
Buffalo |
68.7
81.2 |
73.9
80.9 |
78.3
82.9 |
79.4
82.8 |
87.9
92.4 |
L |
4.94 |
| Feed conversion
ratio(kg D.M./kg gain) |
Ongole
Buffalo |
22.6
21.2 |
14.3
13.8 |
13.7
14.1 |
15.1
14.6 |
13.6
13.5 |
L,
Q |
3.81 |
| Percentage
total intake as rice bran (%) |
Ongole
Buffalo |
0
0 |
19.2
16.8 |
35.6
33.6 |
52.5
49.4 |
59.2
56.9 |
L,
Q |
0.1 |
NS- no significant
effects; L- linear component significant; Q- quadratic
component significant (P < 0.05).
For dairy cows, while concentrate
supplementation is necessary, it is important to
feed optimal levels in order not to be wasteful.
The higher the quality of the forage, the lesser
the quantity of concentrates necessary to achieve
the desired milk yield. Table 5 presents the estimated
amount of concentrates required for target milk
yields in 400 kg milking cows ( non-pregnant with
zero live weight change ) when ad libitum forage
of varying quantities are fed.
The calculations assume that the concentrates were
home mixed and contained 12-2 MJ kg DM and 24 %
crude protein (Devendra, 1975).
Table 5. Required
concentrate intakes (kg DM/ day) for cows fed forages
of varying quality to achieve target milk yields
(Devendra, 1975)
Milk
yield (l/day) |
Forage
quality
Digestibility (or ME in MJ. kg DM) |
| |
|
55 % (7.3) |
60% (8.2) |
65%
(9.0) |
70% (9.9) |
6 |
3.2
|
0.7
|
- |
- |
10 |
4.9
|
2.5
|
0.8
|
- |
14 |
6.6 |
4.8
|
1.1
|
0.3 |
18 |
8.2 |
6.0
|
3.0
|
0,
7 |
22 |
9.8
|
7.7
|
5.4
|
1.7 |
A few studies
have reported the use of supplementing Leucaena
leucocephala to Ongole cattle in Indonesia. Two
of these are especially relevant. In one, the performance
of Ongole cattle offered either grass, sun-dried
leucaena or varying proportions of each. Cattle
offered only grass lost 0.015 kg daily. Bodyweight
gains for diets with 40 and 60% leucaena, 0.544
and 0.587 kg, were significantly higher than for
diets with 20 and 100% leucaena, 0.292 and 0.306
kg daily, and feed conversion ratios were lowest
for the 40 and 60% leucaena diets, 12.0 and 11.3.
Dry matter daily intakes were significantly higher
for the 20, 40 and 60% leucaena diets 92.8, 95.8
and 94.0 g/kg bodyweight (W) 0.75, than for the
100% leucaena, 75.1 g/W 0.75, or 100% grass, 77.6
g/W 0.75, diets. Protein digestibility was significantly
higher for 100% leucaena, 61.9%, than for 100% grass,
53.0%, with other diets intermediate. The leucaena
had average mimosine and DHP (a mimosine breakdown
product) contents of 1.26% and 0.18% respectively.
Plasma thyroxine concentrations averaged 53.3 and
52.9 ng/ml at the beginning of the study and after
20 weeks; there was no significant difference between
treatments. Only 5% of the ingested mimosine and
DHP was excreted in urine and faeces as mimosine
and DHP in cattle offered 100% leucaena. Maximum
benefit was with a minimum 40% of leucaena, there
was no ill effect on animal health when leucaena
was the sole diet.
Rice straw treated with 4% sodium hydroxide and
supplemented with L. leucocephala has been fed to
Ongole and swamp buffalo bulls. Intake of the treated
straw was increased by 30% whereas untreated straw
depressed it by 10-20% leucaena supplementation
increased the rate of passage of digest and balances
of dietary nutrients (nitrogen, phosphorus and calcium)
and levels of metabolites (Moran, Satoto and Dawson,
1983). Studies on phosphorus supplementation in
Ongole bulls and swamp buffaloes from 0.08 to 1.08%
and with calcium, phosphorus ratio varying from
0.14 to 4.58, indicated that both species were able
to maintain positive phosphorus retention on a diet
containing 0.12% P. The relations between P intake
and faecal output plus urinary phosphorus output
and between Ca intake and faecal plus urinary calcium
output were linear in both species (Moran, 1982).
In China, use of cotton seed cake and ammoniated
straw has produced a major impact on improved beef
production (Fan et al., 1993).
5.
Potential performance in indigenous cattle
(i) Dietary nutrients:
There is no doubt
that indigenous cattle are capable of much higher
levels of performance than is evident, conditional
to efficient feeding and nutrition. Central to promoting
maximum performance in these cattle is to ensure
that there is optimum intake of mainly grasses and
or cereal straws on which they are largely dependent.
Beyond this, strategic supplementation is essential,
in which the approach is to provide:
· Feed nutrients deficient for optimal microbial
growth
· Nutrients to increase protein supply for
absorption of the intestine (by-pass protein) and
other nutrients required by the animal (P, Ca etc)
· Potential protozoal toxins to remove the
anti-nutritional effects of protozoa.
· Establish response relationships to supplements
in ruminants fed treated feeds to increase digestibility
(ii).
Supplements :
The supplements
needed to balance low digestibility roughages for
feeding to ruminants are now classified according
to their role as follows (Leng and Devendra, 1995).
· Nutrients essential for efficient microbial
growth in the digestive systems of ruminant, which
include:
- Multi-mineral sources, e.g. molasses or residues
from molasses fermentation (spent liquor), chicken
litter or poultry manure made into loose mixtures,
liquid mixtures or the same mixes solidified into
blocks.
- Non-protein nitrogen sources include urea, chicken
manure/litter and soluble proteins from leguminous
forages, seeds and agro-industrial by-products (e.g.
soyabean curd).
· Supplements that increase protein digested
in the small intestine (i.e. by-pass or escape protein
or rumen non-degradable protein):
- By-pass protein sources which include protein
meals that (a) have been treated in processing (b)
contain a low level of tannins (1-3%), (c) have
simply been dried, or (d) have been heated with
reagents that make the protein insoluble (some protective
agents include xylose, glucose, formaldehyde, gluteraldehyde
etc).
The best preparation and sources of supplements
depend on locality. For example studies have demonstrated
that simply drying leaf foliages has an effect on
how the material is viewed as a supplement (Norton,
1996). The fresh material appears to enhance only
rumen fermentative digestion but the nutritional
value of the dry leaf meal appears to be enhanced
which may be due to insolubility and thus its content
of by-pass protein.
(iii) Examples of
potential improvements:
One of the earliest
studies demonstrating potential improvements to
performance that are feasible concern Kedah-Kelantan
cattle in Malaysia, synonymous with indigenous Thai
cattle and yellow cattle in South West China. It
falls within the thoracic humped cattle category
(Maule, 1990) and has also been described by Mason
(1999). This breed is a descendant of a crossbred
between Shorthorn-type cattle in Western Asia and
Zebus from India, of which the Kangayam and Ongole
are prominent (Devendra et al., 1973). In Malaysia,
a series of studies have been made in the late 1970’s
to demonstrate the potential performance due to
improved feeding and nutrition in this breed. Table
6 summarises the main results. The potential improvements
that are feasible compared to similar cattle in
traditional systems are striking, with the following
magnitudes of improvement:
· Age at first service by 133.9%
· Live weight 24 months by 80.3%
· Carcass weight by 62.4%
· Dressing percentage by 22.8%
· Meat as percentage of carcass weight 18.7%
Table 6. Magnitude
of improvement in Kedah-Kelantan cattle in six important
parameters due to improved nutrition (Devendra and
Lee, 1975).
Parameter |
Traditionalsystem+ |
Improvedsystem++ |
%
Improvement |
| Age at
first service ( Months) |
35.0 |
18.0 |
94.4 |
| Live weight
at 24 months (kg.) |
133.5 |
240.7 |
80.3 |
| Daily live
weight gain from 6 to 12 months (g.) |
145.0 |
339.1 |
133.9 |
| Carcass
weight (kg.) |
81.3 |
132.0 |
62.4 |
| Dressing
percentage (%) |
44.8 |
55.0 |
22.8 |
| Meat as
percent of carcass weight (%) |
69.9 |
83.0 |
18.7 |
+
Refers to farm situations
++Data from controlled experiments
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