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Pigeon Racing and Nutrition of the Muscle
By: Gordon A. Chalmers DVM
As increasing amounts of literature about pigeons
become available, it follows that there are many more informed
fanciers than ever before. Scientific principles in the nutrition,
breeding, racing, and indeed all aspects of the sport are much
more evident even though there are many fads and "secrets"
that continue to hold sway. In terms of diets for racing. For
example, many fanciers are becoming more aware that the flight
muscles of pigeons need the cereal grains such as wheat, oats,
barley, corn, ect. and not, as many British believed for so many
years, the legumes such as peas and beans, as the major fuel:
however, the reasons and basis for the feeding of the cereals
instead of legumes for racing, may not be so well known or understood.
The intent of this article is to discuss the major racing muscles
of pigeons, including their anatomy at the gross, microscopic,
and submicroscopic (electron microscopic) levels, to try to provide
some basic understanding of their function, their fuel supplies,
and just what happens in these muscles from the moment of liberation
at the race pint, to the end of a long, grueling day, and to draw
certain conclusions about these muscles from a nutritional perspective.
By way of introduction I should say that I am not
a nutritionist, but a veterinarian engaged in laboratory diagnostic
work, specifically in the area of pathology, the science of diseased
tissues. I also happen to be a long-time racing pigeon fancier
flying in a small club in western Canada, with modest success.
For several reasons, I was involved at one time in the study of
the muscles of wild animals that were captured through drives
or baited traps. Naturally enough, I had to review information
on normal muscles and to study the effects on these muscles from
physical over-exertion. On e spin-of for me was access to a variety
of scientific literature on the muscles of racing pigeons and
other birds. The opportunity for me, both as a veterinarian and
a racing pigeon fancier, to study these muscles in depth was exciting
and rewarding, as I had never seen anything written on this subject
in pigeon magazines. To this, day I have not seen anything written
in pigeon magazines on the microscopic anatomy of pigeon muscle
and practically nothing on the nutritional needs of racing muscle,
and none of it with much indication of any scientific basis. I
hope that the following information will go a long way toward:
Shedding some much needed light on the subject.
Refuting some of the misinformation and misunderstanding
about the nutritional requirements of the racing muscles of pigeons.
At the outset, it may come as a surprise for many
fanciers to learn that much of what has been determined about
the muscles of birds in general, has been derived from considerable
work on muscles of the racing pigeon, and that much of this work
was don in Canada at the University of Guelph in Ontario, by Dr.
John George and his colleagues and undergraduate students. The
results of this extensive amount of work have been published in
various national and international scientific journals. I believe
that the results of all of this work can be interpreted as I have
recorded them here, and that they represent a reasonable explanation
of events that occur in the flight muscles of pigeons during a
race.
The next item of importance is to realize that there
are two major flight muscles of racing pigeons, as indeed there
are for any flying birds. The first and more massive of these
are the large muscles found on each side of the keel, and are
those we feel with our fingertips as we handle the bird. These
great muscles make up about 20% of the total weight of the bird.
If we kill a bird, place it on its back, head pointing away from
us, and we strip the skin off the underlying tissues, we can see
these great muscles lying on and attached to either side of the
keel. As we look closely, we see that the "grain" of
the muscle runs from the keel in an upward and outward direction
at an angle of about 45 forming a "V" with the keel.
These muscles are known as the major pectorals and are comparable
to the muscles that lie under the breast area of humans, although
they are obviously much more powerfully developed in birds. As
you might expect, the major pectorals are the most powerful flight
muscles in pigeons, as they are in other flying birds: their main
function is to drive the wing through the downstroke, which propels
the bird forward. The other important flight muscles of pigeons
are the much smaller and more deeply located deep pectorals, sometimes
called the minor pectorals, which lie under the major pectorals
right next to the keel. They make up about 3.6% of the total body
weight of a racing pigeon, much less than the mighty major pectorals,
their major function is to bring the wing through the upstroke.
( Incidentally did you know that in flight, the pigeon inhales
during the upstroke and exhales during the downstroke?)
Another important fact to realize is that, in birds,
there are two basic types of muscle, based on the color and function
of these muscles. The first of these is white muscle such as that
seen best in the pale breast muscles of the domestic chicken.
The second is red muscle as seen most prominently in the dark
breast muscles of birds such as pigeons, ducks and geese, among
other flying birds, for example.
Although the muscles of birds contain mixtures of
red and white muscle, it is obvious from the examples cited, that
the breast muscles of domestic chickens contain a preponderance
of white muscle, whereas those of racing pigeons have a preponderance
of red muscle. We will try to explain the difference as follows:
If we take a small piece o the major pectoral muscle, which lies
immediately under the skin of the breast, cut it longitudinally,
ie., with the "grain", process it to produce a thin
section stained with special dyes, and examine it microscopically,
we see that it is composed of many long, cigar shaped units that
are actually specialized body cells called fibers. If we cut the
same piece of muscle in cross section and look end on at the cigar
shaped units, we see that they are more or less round, oval or
even somewhat angular, and that they occur in bundles. (As an
example, we would have roughly the same situation if we took a
number of pencils to form a bundle, wrapped each bundle with an
elastic band and then stacked the bundles on top of one another,
as well as end to end.)
Obviously, hundreds of thousands of bundles, both
stacked and laid end to end, make up the entire muscle we can
feel with our fingers. Continuing our end on view of the muscle
fibers, we not firstly that the vast majority of individual fibers
in a bundle have a narrow diameter. Based on this finding and
several other important and related characteristics which we will
discuss more fully, these narrow diameter fibers have been designated
as red fibers and in fact make up about 94% of the fibers in the
breast muscles. Whereas a majority of fibers are of small diameter,
there are many fewer fibers in a bundle that have a much larger
diameter and are called whit fibers. These fibers make up only
about 6% of the fibers in the breast muscles. We also note that,
for the most part, these white fibers are located on the edge
of each bundle. Once again, if we use the analogy of pencils,
but had mixed thick and thin pencils in a bundle, we would see
that, in general, most of the thick pencils representing white
fibers would be near or actually touching the rubber band, whereas,
most of the slim pencils representing red fibers would be located
more deeply inside the bundle. Thus, the predominance of red fibers
in the breast muscles of the racing pigeon gives that muscle a
red appearance on gross inspection. This red color is related
to the presence of myoglobin, a pigmented, oxygen carrying compound
peculiar to red muscle in many species of birds and animals. By
contrast, the predominance of white fibers in the breast muscle
of the domestic chicken imparts a very pale and characteristic
appearance to that muscle, because white muscle has very little
myoglobin. These basic features serve to outline one of the major
differences between a bird such as the racing pigeon, or any migratory
species which is required to fly for many hours at a stretch,
and a sedentary, non flying bird such as the chicken. There are
other differences and we will explore them in more depth as we
proceed.
In addition to differences in the diameter of these
two types of fibers, what other distinguishing and significant
features are there? Well, major investigations have shown that,
in addition to having a narrow diameter, individual red fibers
have an extensive network of blood vessels running and inter connecting
over their surfaces. Red fibers also have a high capacity to take
up oxygen, because of the presence of myoglobin, for the metabolism
(or burning ) of fuel to produce the energy necessary for flight.
Of very great importance of the racing pigeon is the fact that
these red muscle fibers function (or as we say, they twitch) slowly.
Because these fibers twitch slowly during flight,
they also tire out very slowly. It becomes obvious then that red
fibers are those that can handle the sustained effort of rapid
flight over many miles, whether the distance is a short training
toss, a middle distance race or a major long distance event. In
some special situations such as launching into the air, to be
discussed later, evidence suggests that the red fibers are also
capable of very rapid activity. However, their most important
single function seems to be associated with the prolonged, sustained
muscular effort of distance flying.
On the other hand, we note that the large individual
white fibers have relatively few blood vessels running over their
surfaces and that they have a very poor capacity to use oxygen,
the burning of fuel, the burning of fuel, because they contain
very little myoglobin. In contrast to the red fibers, these large
white fibers function (twitch) RAPIDLY. As you might expect,
because of their capacity to respond quickly, white fibers also
tire out very quickly, and for this reason, it is important to
understand that they can in no way be relied upon for sustained
flight. If they do not function during prolonged muscular effort,
what is their major role? Since white fibers twitch rapidly and
tire quickly, they seem to be most important and useful during
muscular effort that requires very rapid and even explosive bursts
of activity. Thus, white fibers are those that likely operate
most effectively to help launch a bird into the air and allow
it to dodge in the wink of an eye when it encounters predators,
power lines and other obstacles. When your youngsters are dipping
and diving in a frenzy of activity and are all over the sky in
a flash, these functions are probably handled primarily by the
white fibers.
Another important function of these fibers is in
the production of heat in cold weather through the familiar process
of shivering. The trembling wing tips of a in good physical condition
are another example of the function of white fibers. Both of these
situations are good examples that illustrate the rapidity with
which these fibers operate and just what is meant by fast twitch
fibers!
Now, if we were to make use of an electron microscope
and magnify and photograph many thousands of times, both the red
and white fibers, we would see some further striking and highly
important differences between the two. In looking firstly at the
red fibers, we see that they contain many somewhat oval structures
that ten to be present in chains, like beads on a sting, and that
these structures are often separated from one another by what,
at first glance, appears to be an empty space. The oval structures
are known as mitochondria that, for our purposes, can be compared
to a series of furnaces. Naturally, every furnace needs fuel and
these "biological furnaces" are no exception. When we
look closely, we see that the "spaces" between some
of the oval "furnaces" are not spaces at all, but are
actually droplets of an abundant and obvious source of fuel. It
may come as a surprise to many fanciers, but that fuel is, infact,
none other than FAT ! Given the historical ( and incorrect)
belief of some fanciers that protein is the major fuel for racing,
hence, the traditional emphasis by some fanciers on the use of
high percentages of peas and beans as fuel feeds in racing rations,
at the expense of cereal grains this information may be even more
surprising. As we continue to examine the fine structure of the
red fibers, we see that they also contain a considerable number
of granules that have been identified as glycogen, a complex carbohydrate
(or sugar) composed of many smaller units of the sugar glucose,
sometimes also called, dextrose.
The importance of fats as the major fuel for racing,
or for any prolonged flight, such as that of migrating birds,
cannot be over estimated. For example, there is a small songbird
known as the blackpoll warbler that nests each year in the Yukon
and Alaska. As fall approaches, these tiny birds work their way
diagonally south and east across the continent of North America,
feeding and building fat reserves as they travel, until they reach
the Atlantic provinces of Canada and the New England states in
the USA. When fat depots are filled to capacity and the birds
are much heavier, they wait for a high pressure cell moving in
from the west and accompanied by winds from the north or northwest.
When all is ready, the birds launch themselves into the air and
head out over the vast Atlantic ocean. Only when they reach landfall
three to five days latter, on the northeast corner of South America,
do they touch down again, after an incredible non stop journey
for such a tiny land based bird weighing less than two thirds
of an ounce! Without fat, this amazing journey of over 2,400 miles
(3,900 Km.), simply could not take place.
Next month: Part 2
Reprinted with permission from: Dr. Gordon Chalmers,
Lethbridge, Alberta, Canada.
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