Mammals
wildlife preserve in India. Like the African lion, they've suffered from
the destruction of wild lands and from over hunting.
Once, people thought that Asian lions had shorter manes than African
lions, but that's not the case. Both can have either long or short manes.
WOLVES
COYOTE: PLACE IN THE FOOD CHAIN
Every animal on earth lives by eating some other living organism --
plant or animal. The sequence of eaten and eater is called a food chain.
The ultimate source of the energy contained in food comes from the sun. It
is stored in the grass, and passed on to the grasshoppers. The alligator
lizard, which eats the grasshopper, is the next link in the food chain. It,
in turn, is eaten by a roadrunner, which then falls victim to the coyote.
The coyote is called an ultimate consumer because nothing hunts it for
food.
But this food chain is a closed circle, the final link -- coyote --
being fastened to the first -- the grass. When the coyote dies, its
chemicals are broken down by bacteria and returned to the soil, where they
nurture more plant growth.
Like many wild dogs, the coyote is usually active at night, when it
can hunt safely. You can often see a coyote in the early evening and
morning, as it goes to and from its nighttime activities.
Coyotes can run as fast as 40 miles per hour, and at slightly slower
speeds, they can run for miles. If a coyote can stay close to its prey, it
has a good chance of getting a meal.
DHOLE
In hunting style, the dhole is like the hyena. It hunts in a pack with
other dholes, whining, barking and whistling as they go. Whistling usually
means that the hunt is unsuccessful, and the pack should reassemble for
another try.
It is almost impossible for a single dhole to kill a deer, but five to
twelve dholes can manage it together. After the kill, dholes compete for
the morsels by eating very fast. A dhole can chew up almost nine pounds of
meat in an hour.
Strong, wise, brave -- all these words describe the gray wolf. But
another word needs to be added to the list: endangered.
Two hundred years ago, the gray wolf roamed throughout North America.
But many of them were shot by European settlers and pioneers, who were busy
cutting down the wolves' forest home for houses and towns. Those wolves
that remained found fewer deer, moose and beaver to eat.
Today, the gray wolf continues to feel the impact of an expanding
human population. That, and the popular belief that wolves shouldn't live
near humans, continues to threaten their presence on our planet.
GRAY WOLF
Did you know that the gray wolf is the largest member of the dog
family? Apart from man, it once was the most widespread mammal outside the
tropics. As humans move into its habitat, the wolf had to move out.
Did you know that after humans, wolves may be the most adaptable
creatures of all? They're able to live in a wider variety of climates and
habitats than most other animals and can survive on many different kinds of
food.
BEST LEFT UNPROVOKED
Wolves prey on many species in the north -- musk ox, caribou, moose,
deer, hares and even rodents. These carnivores are among the most maligned
of all animals, victims of false myths and legends and systematic programs
of extinction. They are accused of attacking humans and destroying entire
herds of domestic animals. But their depredations of livestock are less
severe than often claimed. And unprovoked attacks by healthy wolves in
North America on humans are unknown. Those recorded from Europe's Middle
Ages are thought to have been by rabid animals or hybrids.
The world will be a far lonelier place if the last wolf dies. As
biologist Ernest P. Walker wrote in his book, MAMMALS OF THE WORLD, "The
howl of the wolf and coyote, which to some people is of more enduring
significance than superhighways and skyscrapers, should always remain a
part of our heritage."
.
PRIMATS
APES: FUTURE
The future of apes is up to us. All of the great apes are already on
the endangered species list, and all of the lesser apes are as well.
Scientists who have studied them agree that all great apes will soon die
out in the wild unless steps are taken now to protect them.
Gorillas and orangutans appear to have no natural enemies, and
chimpanzees have very few. Gibbons, because they move so fast and live so
high up in the trees, are safe from any animal. Nothing could threaten any
of the apes with extinction until man started hunting them, capturing them,
and destroying the wild lands in which they live.
Today, hunting of apes is against the law everywhere, and there are
strict regulations controlling the capture of wild apes. But illegal
hunting and trapping continues. And the greatest threat of all -- the
destruction of wild lands -- grows greater every day. Tropical forests are
being cut down faster today than ever before ... at the rate of one acre
every second, according to a recent report. At this incredible pace, the
homes of many wild creatures -- including apes -- are simply disappearing.
Most endangered of the apes are the mountain gorillas. Today, there
are less than 500 in Central Africa.
And the other apes are not much better off. Nobody is really sure how
many pygmy chimpanzees or bonobos survive in the jungles south of the Congo
River -- but it is probably less than 10,000. There are fewer than 5,000
orangutans still alive in scattered areas of Borneo and Sumatra. And the
numbers of lowland gorillas and chimpanzees are declining rapidly.
Fortunately, there are people who are trying to save the magnificent
apes. In Central Africa, governments are working to protect the last
remaining homes of mountain gorillas. They have even organized guards that
patrol the borders of gorilla preserves to keep the gorillas safe from
hunters. The World Wildlife Fund and other groups are raising money to buy
land and make sure that it will never be taken away from gorillas,
chimpanzees, orangutans, and gibbons. And scientists everywhere are
studying the apes to find new ways to help them.
BONOBO OR PYGMY CHIMPANZEE
Biologists who have studied the behavior of these animals say they are
the smarter of two species of chimpanzees. Their hair is parted at the
middle and wisps out to the sides of the head, giving them an obvious
physical distinction from the common chimpanzee.
Both species of chimps are intelligent. They belong to the select
animals that make and use tools. You might see a chimp defend himself with
a tree branch, or take a twig and turn it into a useful devise for
gathering or eating foods. Chimps also communicate with many gestures and
vocalizations.
People may feel especially drawn to chimps because of some similar
behaviors. Young chimps laugh when they're tickled. Bonobos quarrel over
food, but hug and kiss to make up.
BONOBO: WORKSHOP IN CONSERVATION
The bonobo or pygmy chimpanzee, is one of only four living species of
great apes. The other three species, the gorilla, orangutan, and common
chimpanzee, have received far greater attention until now. Not even
recognized as a separate species until 1929, the bonobo still remains much
of a mystery in its native habitat, the central rain forests of Zaire.
Often confused with the common chimpanzee, the bonobo is only slightly
smaller but has a more graceful, slender body; the head is smaller but the
legs are longer than those of common chimps. The most outstanding physical
difference is the bonobo's hairstyle, an attractive coiffure of long black
hairs neatly parted down the middle. To the experienced eye, the difference
between the chimpanzee and the bonobo is as great as the difference between
a leopard and a cheetah.
The bonobo is as rare in zoos (there are less than 80 in captivity
worldwide) as it is in the wild (estimates range from 5,000 to 20,000). In
1989, the entire San Diego Zoo group of 11 animals was relocated to the
Wild Animal Park.
No effective conservation plan for the bonobo could be developed
without firsthand knowledge of the only country that is home to this
critically endangered ape. International conservation projects are as much
a people issue as an animal issue; therefore, the needs of the local
Zairian people must be taken into account. Political, cultural, and
economic problems are just as important to consider as the biological needs
of the species we are attempting to save. For these reasons, the San Diego
Bonobo Workshop continually emphasizes the need for an international
cooperative effort with the people and government of Zaire.
In light of the increasing awareness of the need to preserve the
world's biodiversity, it is quite surprising how little attention Zaire has
received. The extent and variety of the biological resources in Zaire's
forest ecosystems is matched by few other tropical countries. After Brazil,
Zaire has the second largest tropical forest in the world. Despite this
fact, Zaire is among the last of the countries in the tropical forest belt
without a comprehensive program to protect its tropical forest. Programs
like the one developed at the San Diego Bonobo Workshop will be
instrumental in obtaining funds from organizations like the World Bank to
protect the bonobo and its forest habitat.
THE GORILLA SUBSPECIES
Three subspecies of gorillas are currently recognized. Almost all zoo
gorillas are western lowland gorilla (Gorilla gorilla) native to west
African nations such as Cameroon, the Central African Republic, Gabon,
Nigeria, and Rio Muni. The total population of western lowland gorillas is
estimated to be between 30,000 to 50,000 individuals, and they are
classified as threatened by the IUCN (International Union for Conservation
of Nature and Natural Resources). Studying these gorillas in the wild is
extremely difficult, because their preferred habitat is dense jungle.
A very few eastern lowland gorillas (Gorilla gorilla graueri) native
to eastern Zaire, live in zoos. Mbongo and Ngagi, the two "mountain
gorillas" who lived at the San Diego Zoo in the 1930s and 1940s, would now
be classified as eastern lowland gorillas. These gorillas are considered
the largest subspecies on average, and generally have blacker hair than
western lowland gorillas. They number approximately 3,000 to 4,000 and are
classified as endangered.
No mountain gorillas (Gorilla gorilla beringei) exist in captivity,
but these are the most-studied gorillas in the wild. They live in the
mountainous border regions of Rwanda, Uganda, and Zaire. Only about 600
individuals exist, in two separate populations, and they are classified as
endangered. Mountain gorillas are distinguished physically by their large
size and extra-long, silky black hair. A number of skeletal differences
exist between the three subspecies as well.
It would be interesting to see if DNA sequence comparisons could help
us understand the phylogenetic (evolution of a genetically related group as
distinguished from the development of the individual organism)
relationships of the gorilla subspecies. This could help anthropologists
understand the mechanisms and rates of primate evolution. It could also be
important if gorilla populations ever become so critically depleted that
interbreeding of different subspecies were contemplated. At CRES, we are
comparing DNA sequences from gorillas of all three subspecies. Only a few
gorillas have been tested so far, but to date it appears that the
relationships between the subspecies generally follows the geographic
location of populations.
Western lowland gorillas have a large range, and many DNA sequence
differences exist between different individuals of this subspecies. Western
lowland gorillas are separated by 600 miles from eastern lowland gorillas,
and substantial sequence differences exist between the two groups as well.
The eastern lowland and mountain gorilla populations are found relatively
close together, but they have been isolated from each other for an unknown
amount of time. They are presently separated by substantial geographic
barriers: portions of the Rift Valley and a variety of mountain ranges.
However, we find much less genetic difference between the eastern lowland
gorillas and the mountain gorillas than there is between certain western
lowland gorillas. The distinct physical differences between eastern lowland
and mountain gorillas probably reflect recent adaptations to their
respective habitats -- lowlands versus mountains -- and not a distant
genetic relationship.
LION-TAILED MACAQUES: BACKGROUND
The macaques, a genus of some 13 to 20 species (there is disagreement
among taxonomists on the actual number), are found in North Africa and
throughout southern Asia from Afghanistan to Japan. The most familiar form
is the rhesus monkey, which is often seen by tourists in the towns and
cities of India. Fossils dating to six million years indicate that the
macaques originated in northern Africa and once roamed over Europe as far
north as London. These earlier macaques were not very different in
appearance from the Barbary monkeys that survive today in Morocco, Algeria,
and on Gibraltar. However, once the Macaques reached Asia, at least by
three million years ago, they diversified into a variety of forms. Few are
as distinctly different as the lion-tails, with their black coats, silver
facial ruffs, and strongly arboreal habitats. Lion-tails are one of the two
macaque species that are listed as in danger of extinction, but we may
realistically expect the Tibetan, Formosan, and Sulawesian species to fall
into that category before the year 2000.
Their geographical range snakes along the slope's and highest crests
of the Western Ghat Mountains where, today, the forest is reduced to about
one percent of the total land cover. Like its captive counterpart, the wild
living lion-tail was ignored by primatologists until well into the 1970s.
Although opinions vary, most would agree that the wild population today
numbers between 2,000 and 5,000 individuals. Initial field reports indicate
that wild lion-tails prefer to spend about 99 percent of their time in the
trees. Like other macaques, their diet is dominated by wild fruits, but
includes a variety of flowers, leaves, buds, grasses, insects, and even a
few nestlings of birds and mammals. One of the more interesting forms of
feeding reported by Dr. Steven Green of Miami University involves a simple
form of tool use. In order to protect their hands while feeding on stinging
caterpillars, lion-tails have been seen to pluck large tree leaves and lay
them over the caterpillars before pouncing on them.
In the wild state, lion-tail groups average about 20 individuals,
usually with more than a single adult male present. Males are larger than
females by about a third and are typically ranked relative to one another
in a social hierarchy. Males usually emigrate from their natal group to
join another during the early stages of adulthood. Being macaques, lion-
tails are intensely social and are highly aggressive toward unfamiliar
individuals. Preliminary work on our captive population indicates that much
of the behavior between group members is dependent upon one's relationship
to a small number of female-headed lineages. It is possible to have up to
four living generations within each matriline and four or five matrilines
within a group. Dominance relationships among and within matrilines play a
crucial role in the everyday life of females and their offspring, as they
do for adult males. One's social position determines access to essential
resources such as food, perches, and social partners.
LION-TAILED MACAQUES: FUTURE PLANS
This highly endangered primate has been exhibited at the San Diego Zoo
since 1923. In 1979, the existing population of three males and three
females was relocated to the Primate Research Pad for concentrated study of
their reproductive biology. Within the next decade their reproductive
cycles were characterized, as were their sexual and social behavior,
parturition and infant rearing, and various other aspects of the captive
experience. Nearly a dozen scientific papers from these studies have been
published in peer-reviewed journals or as book chapters.
BY 1989 the Zoo's captive population had grown to 38 individuals. This
same year the program undertook a significant change in direction. Seven
individuals, including five born at the Primate Research Pad, were released
into a state-of-the-art exhibit in Sun Bear Forest. Although these
individuals are no longer under study, it was knowledge gained over the
previous decade that contributed to the design of an exhibit facility
which, by anyone's criteria, is an outstanding success.
A second troop of 11 individuals was simultaneously relocated to the
newly constructed 3/4-acre breeding kraal at the Wild Animal Park. It is
this population which will be a major research focus during the next five
years. This troop has been exempted from Species Survival Plan management,
a program of the American Association of Zoological Parks and Aquariums,
providing freedom to pursue several interesting lines of inquiry. One of
these has to do with the impact of traditional management regimes on
certain life history parameters. The second investigation will pursue
experiments designed to prepare the troop for reintroduction to suitable
habitat in India in five to seven years.
The lion-tailed macaque is by nature a highly social mammal. Group
members are organized in a social hierarchy that appears to remain stable
over many years. Individual troops are highly xenophobic. This trait,
combined with natural aggressiveness, results in potentially fatal conflict
when new individuals are introduced. In the wild state, males will leave
their natal troop at sexual maturity and join a new one. Females remain in
their natal troops throughout their lives.
Transfer by males is accompanied by a substantial amount of
aggression, but is presumably a necessary event to preclude inbreeding.
These natural attributes of wild troops would seemingly have profound
implications for the transfer of individuals, especially of females,
between zoological institutions to satisfy genetic and reproductive
objectives.
It is relevant to ask if the ongoing disturbance of the social order
through frequent inter-institutional transfers might negatively impact on
such parameters as infant mortality, female fecundity, and perhaps even the
neonatal sex ratio. Our kraal group has been together for the past 24
years, the only social disturbances having been the replacement of breeding
males. We have learned how to integrate new males into groups with a
minimum of social upheaval. We therefore have a unique opportunity to
compare findings from our relatively undisturbed population with those from
more traditionally managed populations in other zoos over the next several
years.
Preparation of this same troop for reintroduction to the wild has two
components. The first entails a number of experimental procedures designed
to "teach" natural foraging, avoidance of predators (including humans), and
appropriate social cohesiveness. In addition, the troop must be routinely
evaluated for any pathogens that would pose a hazard to the existing wild
population.
The second component is evaluation of potential release sites in the
wild. The area selected for a test-case reintroduction must not only be
protected from human activity, but must contain adequate food and shelter
to insure the long-term survival of the troop. CRES anticipates working
closely with Indian colleagues on this aspect.
NIGHTTIME IS THE NORM: LABOR AND BIRTH IN THE LION-TAILED MACAQUE
Lion-tailed macaque neonates (newborns) are born with black fur, and
their faces, hands, and feet are pink and hairless. Their characteristic
silver manes do not begin to grow in until the babies are several weeks
old, and their faces gradually acquire the black pigmentation of adults.
When the lion-tailed macaque breeding and management program began at
the CRES primate facility more than ten years ago, little was known about
the gestation, labor, and delivery of infants in this species. There was
extensive documentation of parturition in some other macaques, but no
comparable data were available on the much rarer lion-tailed macaque. How
long is the normal gestation length? At what time are births most likely to
occur? How long does labor last? What factors indicate that there may be a
delivery problem requiring veterinary intervention? Answers to these and
other important questions were needed in order to ensure the best captive
management procedures and to maximize the breeding success for this
species.
The primary reason these data had not been collected previously is
that most new infants were usually discovered in the morning, after the
keepers arrived at work. We began collecting data on each lion-tailed
macaque birth by setting up 24-hour "birth watches" that began several days
before the dam was due to deliver. Conception dates were determined
partially through hormone data from daily urine samples, and also by
keeping careful track of menstruation, sex-skin swellings, and mating
episodes. Parturition-date predictions were based on the 168-day gestation
length documented for the rhesus macaque. However, because this is an
average length, we began our observations about ten days before the due
date in order not to miss the early deliveries.
The birth watch involved round-the-clock observations at 15-minute
intervals during successive, 4-hour shifts. Observations were recorded by
keepers, technicians, and trained volunteers. As soon as any signs of
straining or birth fluids were noted, continuous notes were kept and each
subsequent contraction or birth-related event was timed and recorded.
Behavioral indications of impending labor included restlessness and manual
exploration of the vaginal area. Although these signs eventually proved
reliable, we used the first, clear contraction as the starting point for
measuring the duration of labor. (In human terms, this is equivalent to
second-stage labor. The usual criterion of first-stage labor, cervical
dilatation, cannot be observed in the wild primate unless restraint is
used.) During actual labor, several straining postures were noted; most
common were variations of squatting postures and arched-back stretches.
The first birth was to an experienced mother (this was her third
delivery) and was documented on videotape. After nearly 8 full hours of
labor and 188 contractions, the dam gave birth to a healthy, female infant.
These initial observations led us to believe that a labor of this duration
was not a basis for concern; however, we soon learned that this was far
beyond the average labor length and number of contractions common for this
species.
Over an 8-year period, we were able to collect data on 18 births from
8 different mothers in our colony. Our program has provided some valuable
information about species-typical birth patterns that we can now use to
direct management decisions. We found that the average length of labor to
expulsion of the fetus was about 2 hours and 15 minutes, and the shortest
labor was only 50 minutes total. The female that required eight hours to
deliver in the first case observed then delivered her subsequent infant in
only a little over an hour! Although our sample is still small, it would
appear that, on the average, first-time mothers have longer and more
difficult labors.
Our study determined that the average number of contractions to
delivery for lion-tails was 54. The female with the longest labor also had
the largest number of contractions (454). In her next delivery, the infant
arrived after only 14 contractions, the lowest number recorded during the
entire birth study. Based on the average number of contractions seen in 17
successful deliveries, and one ending in stillbirth, contraction
frequencies approaching 75 to 100 in number may serve as a warning that
intervention will be necessary.
The average length of gestation for 14 pregnancies in our colony was
169.5 days, with a range of 163 to 176 days. This is very similar to what
has been reported for other macaques. Our observers quickly discovered that
those who watched during the 7 to 11 P.M. shifts were the most successful
at being present when births occurred: labor began between the hours of
7:15 P.M. and 3:15 A.M. in every case but one. The exception was one first-
time mother that began straining in the early afternoon. This female had a
difficult labor, and a dead fetus was later removed by cesarean section
after 8 hours of straining and 193 contractions. All the other births
resulted in live offspring and occurred between the hours of 8:05 P.M. and
6:28 A.M. Based on previous primate birth records, daytime births are not
the norm and may indicate an increased risk to both fetus and dam.
Expulsion of the placenta always took place within about 20 minutes
after parturition, and usually it was immediately consumed by the mother.
In a few cases, first-time mothers carried the placenta around for several
hours, along with the infant, until it could be removed by keepers.
Whenever possible, a sample of the placenta is saved for analysis by Zoo
pathologists, who check it for abnormalities. After delivery, the mothers
carefully lick the birth fluids off their infants, and the neonates begin
nursing within a few hours. Each and every female in the study provided
excellent maternal care immediately following parturition.
The lion-tailed macaque breeding colonies are now located in the Sun
Bear Forest exhibit at the Zoo (one adult male and six females) and in a
large, off-exhibit kraal at the Wild Animal Park (one adult male, two
juvenile males, one infant male, and ten females). Together these represent
the largest captive group of lion-tailed macaques in the world -- about 20
percent of the total captive population. Eight years of patient monitoring,
birth watches, record keeping, and evaluation have brought us a long way in
the breeding and captive management of this macaque species.
ZOONOOZ, May, 1990 "Nighttime Is the Norm: Labor and Birth in the Lion-
tailed Macaque," by Helena Fitch-Snyder, Animal Behavior Specialist/CRES
and Donald Lindburg, Ph.D. Behaviorist/CRES.
MORE ON IGUANAS
The environment in which a lizard lives may determine how easily its
scent marks can be located by other lizards. Both desert iguanas
(Dipsosaurus dorsalis )and green iguanas (Iguana iguana) possess femoral
glands on the underside of the hind legs. They use pheromone secretions
from these glands to mark their territories. Desert iguanas live in
extremely hot and arid habitats, whereas green iguanas live in humid
tropical forests. Because these two species of lizards live under such
different environmental conditions, it is not surprising that the way their
pheromone signals are transmitted differs.
Desert iguanas have scent marks that are nonvolatile, which means that
they evaporate very slowly into the atmosphere. These marks are also
extremely resistant to chemical breakdown at high temperatures. The low
volatility and thermal stability of desert iguana scent marks ensures that
they persist under harsh desert conditions, a necessary quality if they are
to be used effectively for territory marking. Although these
characteristics make scent marks more durable in desert environments, they
pose a problem for desert iguanas attempting to detect them if the marks
are not volatile; they may be difficult or impossible to locate using
smell. Desert iguanas avoid this problem by combining a unique type of
visual signal with their scent marks.
One striking property of desert iguana scent marks is that they
strongly absorb ultraviolet light. Although these wavelengths are invisible
to human eyes, they appear dark to animals able to see ultraviolet light --
much as ultraviolet-absorbing honey guides on flowers look black when UV-
sensitive camera film is used to view them. Recent studies have shown that
desert iguanas are able to see long-wave ultraviolet light, and they may
use this adaptation to detect scent marks from a distance. After scent
marks are localized using visual cues, desert iguanas can approach and
investigate them in more detail through tongue-flicking. Although it is not
known to occur in mammals, visual sensitivity to ultraviolet light has been
shown in certain insects, spiders, fish, frogs, and birds. The ability of
desert iguanas to detect ultraviolet light may help them solve some of the
problems associated with finding scent marks in a desert environment.
In contrast to those of desert iguanas, the scent marks of green
iguanas contain a variety of volatile chemical compounds, and they do not
absorb ultraviolet light. Behavioral studies indicate that green iguanas,
unlike desert iguanas, can detect these scent marks by smell alone. Because
the chemical components of green iguana scent marks remain active and
transmit well under the humid conditions of tropical forests, green iguanas
do not appear to need a visual cue in order to locate scent marks. Research
on both iguana species demonstrates how the environment in which animals
live can influence the nature of the communication signals they employ.
Страницы: 1, 2, 3
|