Although
it is well known that the absorption and utilization of a particular mineral
can be significantly affected by the presence of other minerals in the ration,
by far the greatest influence on availability is due to the level of intake of
the mineral in question. The classical example to illustrate this point is the
absorption of calcium. Although 98% of the calcium is contained in the bones
and teeth of animals, the remaining 2% is essential for the transmission of
nerve impulses, muscle contraction, blood clotting and numerous enzyme
activities. For this reason, the concentration of calcium in blood is
maintained within a relatively narrow range. This regulation is achieved
through a system of hormones and target organs which release and take up
calcium depending on the concentration of circulating hormones. This is
illustrated in Figure 1.

Fig 1.
Factors involved in maintaining blood calcium concentrations
(Classical control by feedback loop)
In
this way calcium availability decreases as the calcium intake increases. When
the animals requirement for calcium is exceeded, absorption ceases regardless
of intake. As an animal ages not only does calcium absorption from the gut
decline but the ability of the skeletal bone cells to release calcium also
diminishes (calcium absorption has been recorded at virtually 100% in a milk
fed calf and falls to approximately 20% of intake in older animals). For
these reasons there is a higher incidence of uterine prolapse and milk fever in
older cows.
Although
calcium absorption is controlled by this hormone regulated feedback loop, the
efficiency of absorption of other minerals is influenced directly by the
dietary intake of the mineral in question. This is sometimes expressed by the
statement that “a deficiency of a mineral sensitizes its absorption”. The
minerals phosphorus, iodine, iron and especially zinc exhibit this phenomena.
There
are however very clear interactions between different mineral elements which
influence availabilities. These interactions have been investigated for many
years and a summary of known interactions is presented below in Table 1.
Table 1 –
Minerals showing interactions with other minerals/nutrients which can influence
availability.
| Mineral | Interactive Nutrient
|
|
Calcium | Phosphorus, Zinc, Silica, Sodium
|
|
Phosphorus | Calcium, Zinc, Sodium
|
|
Magnesium | Calcium, Potassium, Sodium, Iron, Ammonia & Fatty Acids
|
|
Sulphur | Magnesium
|
|
Sodium | Calcium, Phosphorus
|
|
Zinc | Copper, Manganese, Calcium, Phosphorus, Cadmium, Lead
|
|
Copper | Molybdenum, Sulphur, Zinc, Iron, Calcium, Cadmium, Lead
|
|
Manganese | Calcium,Phosphorus, Zinc
|
|
Iron | Calcium, Phosphorus, Cadmium, Cobalt
|
|
Molybdenum | Sulphur, Copper
|
|
Selenium | Sulphur
|
However,
the mineral interactions which have the most impact on the health and well
being of animals are as follows:
(i)
Copper,
Molybdenum and Sulphur
(ii)
Copper
and Zinc
(iii)
Magnesium,
Potassium and Sodium
COPPER,
MOLYBDENUM AND SULPHUR
The
antagonism between copper, molybdenum and sulphur is without doubt the most
widely researched example of adverse mineral interaction. Copper deficiency
has become recognized as one of the most important nutritional factors
confronting livestock around the world. In countries which have high rainfall,
organic peat type soils which are poorly drained, molybdenum levels in pasture
can be very high (20-100mg/kg DM). The availability of dietary copper is
reduced by this high molybdenum concentration especially when sulphur levels in
forage are low. In contrast, on very high sulphur intakes which generate a
good deal of hydrogen sulphide in the rumen, molybdenum can actually help to
prevent copper deficiency. High levels of hydrogen sulphide produced in the
rumen result in the formation of copper sulphide which is unavailable to the
animal and is excreted in faeces. Molybdenum in this situation helps to
prevent the production of hydrogen sulphide and thus prevents the formation of
insoluble copper sulphide.
Unfortunately
to really make the situation even more complex, at low/normal sulphur levels in
a herbage which is also low in copper, the addition of molybdenum can actually
cause copper deficiency. In this situation free from interfering high levels
of rumen sulphide, the copper and molybdenum ions can complex together in the
rumen to form copper molybdate which is excreted through the kidneys.
Superimpose
on this situation the ingestion of soil and its mineral content, (especially
iron) it is easy to see the complexities of the interactions which have led to
conflicting results under field conditions.
COPPER AND
ZINC
Copper
and zinc both compete for the same absorption sites in the gut and for this
reason a mutual antagonism exists. High levels of copper interfere with the
absorption of zinc and vice versa. Cattle grazing temperate pastures in the
south of the country during the summer months can run the risk of facial eczema
caused by fungal toxins. Zinc given in the feed or water supply has been shown
to be highly effective in preventing liver damage caused by these toxins.
However, prolonged treatment with high levels of zinc will also predispose the
animal to copper deficiency.
Finishing
diets for beef cattle usually contain commercial trace element mixtures. Of
the seven minerals (cobalt, copper, iron, iodine, manganese, selenium &
zinc) considered essential for feedlot cattle, zinc concentrations usually show
the greatest variations in such mixes.
In
one American survey of feedlot consultants, Galyeen (1996) observed that zinc
fortification ranged from a low of 24-30 mg/kg of feed to over 300mg/kg. Many
Nutritionists believe that high dietary zinc levels are necessary for improved
immunity, hoof health and carcass quality. The scientific evidence however,
for beneficial effects of super nutritional levels of zinc above the levels
recommended by the NRC (30-40 mg/kg feed) is scanty at best.
High
levels of zinc in such situations may not only be antagonistic to copper
availability but also impose an unwanted environmental burden by increasing
zinc levels in manure.
Limestone
additions to diets have also been implicated in a reduction in zinc
availability to the beast. This is certainly true in monogastic animals.
However, several good quality research studies have revealed very little
influence of calcium carbonate on the availability of zinc in cattle.
As
stated previously, zinc is one of the minerals which is absorbed more
efficiently when dietary concentrations are reduced. It is questionable
whether high levels of zinc in feed are really necessary except in
circumstances such as the prevention of facial eczema in cattle.
POTASSIUM,
SODIUM AND MAGNESIUM
Although
magnesium is a vital element necessary for the well being of animals there
appears to be no hormonal regulatory system as in the case of calcium. In
spite of this, magnesium related disorders do not exist in simple stomach
animals. In cattle however, low magnesium disorders (hypomagnesaemia) are very
common. This is particularly true of cattle production systems based on high
nitrogen grasses in temperate areas or in green oat finishing systems in
central and southern Queensland. Tropical grasses usually contain higher levels of magnesium
than temperate grasses. Magnesium is absorbed primarily through the rumen and omasum
(book organ) in both cattle and sheep. Absorption of magnesium is markedly
decreased by high potassium intakes but enhanced by high sodium intakes. Young
grasses are low in sodium and due to intensive use of potash fertilizers
usually contain high levels of potassium (3-5%). For this reason cattle in the
south are at greatest risk from hypomagnesaemia especially if the areas are
subject to occasional low temperatures which promote a decrease in magnesium
concentrations in leaf material. (Magnesium is withdrawn into the root of the
plant during periods of cold stress).
High
potassium intakes prior to calving predisposes the animal to disorders centered
around poor calcium metabolism. Potassium itself does not interfere
significantly with calcium availability. It is the mobilsation of calcium from
bone which is reduced when potassium levels in diets for dry cows are
excessive.
BIOCHEMICAL CHANGES IN
THE COW IN RESPONSE TO AN INCREASED NEED FOR CALCIUM
On the day
of calving the cow can produce 10 litres or more of colostrum containing in
excess of 25g of calcium.
An
insufficient rate of calcium release from body reserves coupled with high
output of calcium from the body is the prime cause of milk fever. However, as
cows become more and more productive and therefore under greater metabolic
stress, we are seeing an increase in the incidence of subclinical milk fever or
"sad cows". Dry matter intake in such animals is generally reduced
and milk production is below target levels.
Insufficient
calcium mobilisation at this time also can result in increased difficulty in
calving, increased retention of afterbirth, rumen stasis, displaced abomasum
and increased mastitis.
First
lactation cows almost never develop milk fever. They may experience some
degree of hypocalcaemia during the first days of lactation but their intestine
and bone adapt rapidly to the calcium demands of lactation. As the cow ages
however:
The adaptation process slows
There is decreased absorption of calcium from the intestine
As stated
previously the increased resorption of bone calcium is under the control of an
active Vitamin D metabolite - 1-25 dihydroxy vitamin D (1-25 (OH)2 D3)
which is produced by the kidney in response to parathyroid hormone
stimulation. However it has been shown that levels of the active metabolite
can actually be higher in the blood of some cows which suffer from milk fever.
This has led to the hypothesis that cows with this condition have a reduced
sensitivity to 1-25(0H)2 D3 preventing them from
increasing calcium availability.
It is now
believed that slight metabolic acidosis is important to allow the hormones and
metabolites to function efficiently in order to mobilise calcium from bone. For
this reason the acid-base balance of dry pregnant cows has been investigated.
The
concept of balancing rations for cations and anions is not new. Dishington
(1975) successfully prevented milk fever in 92% of cases when prepartum dairy
cows were fed a ration containing negative Dietary Cation-Anion Balance (DCAB)
and high calcium content.
The
Dietary Cation-Anion balance refers to the proportion of specific ions in the
diet. This can be a very confusing concept. It is generally considered that
anions form acidic residues and cations form alkaline residues. This is
incorrect. For example HPO42- and NH4+
both act as proton donors (alkaline buffers) even though one is a cation and
the other an anion.
The
important concept is that the dietary cation-anion balance does not determine
the acidogenic or alkalogenic properties of the feed. It does however affect
the metabolic processes within the animal.
The most
commonly used expression for DCAB is:
Meq
[(Sodium + Potassium) - (Chloride + sulphur)]
100g Diet DM
To
calculate DCAB (Meq/100g DM)
[(%
Sodium in diet + % Potassium in diet)] - [(% Chloride in diet
+ % Sulphur)]
0.023
0.039 0.0355 0.016
It has
been found that while lactating cows require a positive DCAB, it is important
to have diets for dry cows in the 3 weeks prior to calving with a negative DCAB
or close to negative DCAB as possible.
Negative
DCAB in rations for pre partum cows prevents a decline in blood calcium at the
initiation of lactation by one of the following mechanisms.
By increasing the rate of bone calcium mobilisation directly.
Increasing the rate of bone mobilisation of calcium indirectly via increased excretion of calcium. Early work suggested that the salts effected changes in the intestine which increased the digestibility of calcium. However more recent research has not
confirmed this.
Excess
anions in relation to cations can produce metabolic acidosis. Chronic acidosis
increases urinary excretion of calcium. This clearance of calcium stimulates
the release of parathyroid hormone and synthesis of 1-25 (OH)2 D3
which mobilises bone calcium.
More
importantly however, it has been shown that an excessive basic environment
within bone cells inhibits the activity of the osteoclasts (insensitive to the
metabolites) and therefore the rate of bone mobilisation falls.
For this
reason reducing the daily potassium intake before calving is very important.
Molasses and dunder both contain large amounts of potassium and are often not
fed to dry cows before calving for this reason. However, both supplements
contain large amounts of chloride and are therefore DCAB neutral and do not
present a problem for dry cows.
Magnesium
and calcium are also implicated in transit tetany. During transport some
animals (perhaps the more excitable) in a herd can become staggery and may be
tramped on in the truck resulting in bruising or even death. Cattle leaving
the warmer north of the state for saleyards and feedlots in the colder south
sometimes suffer from this disorder. Allowing animals access to a mineral
rich supplement prior to shipping aids significantly in this regard.
Supplied by Dr. Robert Elliott.