Professional Documents
Culture Documents
PREFACE
Going lower to get higher
The pastoral regions of Ethiopia are traditionally lowland, namely those areas less
than 1500 meters above sea level (masl). The most extreme of these is the Afar
Triangle which at its lowest point is to 116m below sea level in temperatures range
from 25C in the rainy season to 45C in the dry season. . It can be said that it is the
opposite of the polar regions of our planet where only thermophilic species and
life style can survive.
The lowlanders are linked to the highlanders socially and economically via what is
called the string of nature: water is discharged in the form of rain on the mountain
roofs of Ethiopia and agriculturalists plow and cultivate cereals. Streams run to the
lowland plains forming several perennial rivers which are the last refuge of
pastoral people during the driest periods.
The pastoral area of Ethiopia is the main camel belt in the horn of Africa. It is
known by a camel culture, a monoculture which is expressed as adaptation to arid
ecology through dependence on the camel which is based on uniform husbandry
methods and mobility.
The camel is the only large mammal capable of inhabiting the arid lowlands.
Although official surveys estimate a total camel population of some two million
head in Ethiopia this is most likely an under-estimate. The unique geographical,
economic, social and cultural fabric of this biosphere is less known to the outside
world even to many Ethiopians, as pastoralists were marginalized in the past.
Furthermore, Ethiopia was considered as terra incognita vis a vis camel pastoralism
and camel research.
In this book we tried to distill the scattered and scanty literature on Ethiopian
camel, the pastoralist, the environment, the market and camel health and
welfare.We relied heavily on our experience of the past 25 years of on and off
teaching and research on camels, blended with results and experience from other
countries.
The economic importance and adaptive value to climate change of the camel are
on the rise which means that camels are considered as a priority for policy makers
and researchers. Thus it is timely to compile such information in the form of book.
Although camel production and health has, for the past last three decades,
featured in the curricula of Ethiopian Veterinary and Agriculture colleges there has
been no textbook on Ethiopian camels. This book is intended for undergraduate
veterinary and animal science students, policy makers and researchers.
We are grateful to the following organizations organizations and all people who
helped us in the preparation of this book, including FAO, for finacing the book
project. The Ethiopian Veterinary Association (EVA) for coordinating and
supervision of the project, Dr. Abrha Tesfay, Mr. Sirak Alemayehu for generously
providing some of the photographs and those people who shared their
photographs in public domain with no copyright restrictions, and Dr Peter
Morehouse for taking his valuable time to go through all the cahapters of the book
If Mona Lisa is mysterious art then the camel is a mysterious creature
Melaku Tefera
Associate Professor
College of Veterinary Medicine, Haramaya University
P.O.Box 144 Haramaya Campus. Ethiopia.
251-0914722459,
< melaku22@yahoo.com >
Getachew Abebe
Professor,
Food and Agriculture Organization of the United Nations,
Addis Ababa, Ethiopia
FOREWORD
The camel which is an economically, socially and environmentaly important animal
is the least studied domestic species. The writing of such book is timely and will
rekindle camel research in Ethiopia. Haramaya University being located at the
pastoral and agropastoral interface has served as a brige between the highland
and the lowlands research over the last 50 years. The camel research center at
Babile and the Institute of Pastoral and Agropastoral at Haramaya University
contributed to the meager research on the camel. This book is a culmination and
milestone in camel research in endeavour Ethiopia.
The camel as the bonanza of the drylands has an incomparable advantge
compared with other livestock as it is the only livestock species capable of
producing meat and milk when all other animals are limited by dehydration.
Furthermore most of its products are nutritious, healthy and have medicinal value.
This book attempts to create awareness of these aspects.
Indigenous knowledge provides the basis for problem-solving strategies for local
communities. The most important element to survive in the drlands is knowledge.
A key factor is balancing livestock with the available plant biomass and moisture.
The pastoralist experience of severlal millena is incorporated in this book.
Intensification of camel production and advances are blended to encourage
alternative techniques to extensionists, development professionals and
researchers.
The book, emphasizes on the importance of the camel husbandry in a holistic
approach as a result it is of value to government bodies and policy makers in
addressing climate change and sustainable livelihood.
This book being the first on Ethiopian camels, is educative, informative and will
inspire and guide young Ethiopians to pursue carrierrs on camel.
one man camels safeguards for he owns them legally
another man does so for the benefits he from them derives
while a third man does so, too for the love he for the camel has
(Somali oral tradition; Abokor, 1987)
CONTENTS
CHAPTER ONE: INTRODUCTION
The dry land ecosystem
Pastorlalism and pastoralists
Camel pastoral tribes
CHAPTER TWO: CAMEL FEED, FEEDING AND NUTRITION
Feed and Feeding of Camels
Brows species of Camels
Salt Lick and Water Resources and Management
Watering
CHAPTER THREE: CAMEL BREEDS AND BREEDING
Breeds
Breed classification based on location
Breed classification based on production performance
Reproductive performance of male camel
Reproductive performance of female camel
CHAPTER FOUR: CAMEL PRODUCTS AND PRODUCTIVITY
Meat
Milk
Camel Hides
Work Performance (pack and transport)
CHAPTER FIVE: CAMEL MARKETING AND ITS VALUE CHAIN
Milk marketing
Milk market value chain
Structure of the livestock Supply markets
Primary market
Secondary market
Terminal markets
Live animal and meat export value chains
CHAPTER SIX : CAMEL WELFARE
CHAPTER 7: DISEASES OF CAMEL
Bacterial diseases
Viral diseases
Parastic diseases
Saddle soures and wounds
CAHPTER 8 :CAMEL RESEARCH AND THEWAY FORWARD
ANNEX
REFERENCES
32
49
68
85
110
118
151
159
169
I
I
CHAPTER 1: INTRODUCTION
Melaku Tefera,
College of Veterinary Medicine, Haramaya University, P. O. Box 144, Haramaya
Campus, Ethiopia, melaku22@yahoo.com
The camel is a versatile animal; it can be milked, ridden, loaded, eaten, harnessed
to plow or wagon, traded for goods or wives, exhibited in zoos or turned into
sandals and camel hair coat (Faye, 1997). Despite the vital role of the camel in the
arid zones its status vis a vis disease is not different from other domestic animals
(Tefera, 1985).The camel in Ethiopia is not well studied. Camels are raised under
traditional management systems details of which are not well documented.
Pastoral camel production is under pressure because of multiple changes in the
production environment (Scoones, 1994). Increasing human population pressure
on pastoral grazing areas and the economic implications resulting from diseases
and lack of veterinary services are some of the factors that adversely affect
traditional camel production (Tefera, 2004). As camel owners become sedentary,
the camel disappears. In many places of the world the development of
infrastructure, especially roads, has caused the camel to lose its value as a riding
animal or beast of burden. Despite the ecological, economical, environmental and
social benefits of the camel it has remained the least studied domesticated animal
(Payne, 1990). One reason is the main camel belt area is located in three poor
countries, namely Ethiopia, Somalia, and Sudan accounting for 60% of the world
camel population (Mukassa Mugerewa, 1981). The objective of this chapter is to
document the origin distribution of the camel and to describe the habitat of the
camel and the pastoralists in Ethiopia who look after them.
1.1. Origin and distribution of the camel
All camels in Ethiopia are dromedaries (Camelus dromedarius). The history and
origin of the domestic camel remain elusive when compared with those of cattle
and small ruminants. A molar tooth and metatarsal bone was found by a team of
Paleontological researchers in Ethiopia in the lower Omo valley, and these the
fossils date from 2.6 million year ago (Pleistocene) and seem to be those of
Bactrian camels. These are the first camel remains to be recognized in eastern
Africa (Howell, et al. 1969). However during the Holocene period Bactrian camels
became extinct in Africa (Kohler, 1993 cited by Getahun, 1998). The one-humped
camel or dromedary is generally thought to have evolved from the two-humped
Bactrian species. This theory is partly based on embryological evidence showing
that during prenatal development the dromedary fetus actually has two humps De
la Tour, 1971 (Cited by Mukasa Mugerwa, 1981) while a vestigial anterior hump is
present in the adult. Williamson and Payne (1990) speculate that the one-humped
species probably evolved in one of the hotter and more arid areas of western Asia.
Dromedaries were probably domesticated in coastal settlements along the
southern Arabian Peninsula somewhere between 3000 and 2500 BC (Wilson,
1984). Once in Africa, Mikesell (1955) suggests that the camel spread west and
southwards from Egypt, although Bulliet (1975) is of the view that the camels of
the Horn of Africa are more likely to have come across the sea from the Arabian
Peninsula than spread southwards from Egypt and Sudan. Curasson (1947) and
Epstein (1971) indicate that the dromedary was introduced into North Africa
(Egypt) from southwest Asia (Arabia and Persia).
The camel was introduced into Ethiopia around 1000 BC. There are historical
accounts describing the Queen of Sheba of the ancient Abyssinia kingdom at the
head of a caravan of riches when she visited Israel's King Solomon and established
trade in the Middle East. However, other reports suggest that camels were
introduced into Eastern Ethiopia around 500 AD together with the introduction
and spread of Islam. (Tefera, 2004). Archeological evidence shows that a camel
tooth was discovered in Axum probable date 500 AD (Philipson, 1993). Cave
Paintings of LegaOda near Diredawa presented as Figure 1.2, dated to the 1st
centuary AD depict a camel. Thus the camels in North and Eastern Ethiopia appear
to be distinct breeds and two routes of introduction were suggested as shown on
Figure 1.3.
The domestication of the dromedary, like many other domesticated mammals, has
promoted unprecedented progress in cultural and economic development of
human societies, representing a
great leap forward for human
civilization.
In Ethiopia camels were involved in the salt trade when salt blocks locally known as
Amole were used as money in trading goods.
All camel raising areas In Ethiopia have many similarities and one can conclude
that it is a mono culture.
In 1985, the camel herd was growing annually by 2.5 %. Taking the following
parameters as determined in our study: e A= 60 %, B= 10% C= 2 years. D= 0.5 and
E=10%.
1.3 The dryland ecosystem
Ethiopia is topographically classified into two areas: highland and lowland. The
periphery encircling the country generally consist of lowland plains, with an
elevation below 1500 masl and mean annual rainfall below 500mm. The lowlands
cover some 65 million hectares (61%) of the total area of Ethiopia and consist
mainly of rangeland which is home to 12% of the human population and 26% of
the livestock (Coppock, 1994). The climate in the lowlands is arid and, owing to the
unreliable rainfall, the ecosystem in these environments never achieves
equilibrium between grazing and fixed number of settled livestock. With increasing
drought and erratic rainfall, cultivation of land is difficult and crop failure is
common resulting in reduced per capita food production. Thus, traditional
pastoralism constitutes the only efficient means of exploitation of the dryland
resources (Payne 1990; Wilson 1984) otherwise heavy investment or irrigation and
moisture harvesting technologies would be required.
In the drylads where
biomass is meager,
resource utilization should
be optimized through
appropriate livestock
production system
(Njeuru, 1996). Multiple
herd species have
ecological and
socioeconomic adaptive
value, risk spreading and
conservation of resources,
identified as energy
extraction pathways: a)
the reliable pathway,
shrub-camel-milk-human,
b) the opportunistic
pathway grass-cattle-milkhuman and c) contingency,
sale for cash pathway grass-small stock-meat-human as shown in Table 1.1. Camels
cause less environmental harm compared to other livestock species (Schwartz and
Dioli 1992). As climate change is drastically altering the global landscape, camels
raising could become an alternative livelihood which is second to none. In
Table 1.1: Data on rainfall, evapotranspiration and aridity index for 250 stations in Ethiopia
(Hawando, 1995)
1.3.4 Rainfall
Unlike temperature and potential evapotranspiration, rainfall shows considerable
variability within the region in both space and time. Therefore it is closely
associated with rangeland vegetation pattern. Rainfall is highest in the highland
areas where up to 2000 mm/year of rain falls and lowest along the eastern border
with 250 mm/year. Rainfall is highly seasonal and either unimodal or bimodal. The
timing of the rainy season also varies. Mean annual rainfall is not considered in
itself to be the best climatological indicator of the influence of rainfall on plant
growth. Rainfall in eastern Africa is highly erratic and unreliable in terms of amount
in- time and space. For instance Ellis, et al 1993 found annual rainfall to have
varied from 85% to 12% of the long term mean over 63 years. Dry years were more
common than wet periods. Arid regions differ from wet regions only in having
more evapotranspiration per year.
High intensity rainfall causes significant increase in surface runoff, which results in
large amount of water becoming inaccessible to plants. The greater the loss by run
off the less effective rainfall is in supporting plant growth. Tropical regions tend to
have higher intensity rainfall than temperate regions. Rainfall events as high as
279-381 mm/day have been recorded in eastern Africa (Pratt and Gwynne, 1977).
Minimal requirements regarding the amount of rainfall, the period of time over
which it occurs and the ratio of rainfall to potential evapotranspiration must be
met to initiate and maintain growth of range land plants. In order to initiate
effective growth (of annual grasses) in arid areas a minimum of 15 mm of rainfall
must fall within a week, the first rain must wet the seed for at least 3 days, and
enough rain must fall to compensate for evaporation. However, under the high
potential evapotraspiration typical of arid eastern Ethiopia, growth is still
insignificant with rainfall of 25 mm over a 10 day period which exceeds a quarter
of the potential evapotranspiration that is usually enough to initiate growth in
semi arid range lands. King (1993) reported that, about 25 mm of precipitation is
needed for growth of perennial grasses and shrubs and 40-60 mm for seed
germination of annual grassland.
1.3.5 Soil
Soils reflect the influence of climate, parent material, topography, time and living
organisms (principally vegetation). The stronger influence of climate, in this case
rainfall, is seen in the broad regional soil units of Eastern Africa. The specific nature
of local soil types as reflected in their depth, horizonation, texture, color, fertility,
etc which results from the degree to which the parent material, topography and
time (in particular) combine to interact with and modify the effects of climate on
soil development. Thus rangeland areas which share the same climate but which
differ in terms of topography, underlying parent material or geological age are apt
to have different soils.
rainfall gradient the major woody growth changes from tree to shrub to dwarf
shrub. Forage produced by trees, shrubs and dwarf shrubs is especially important
in arid and hyper-arid environments where herbaceous productivity is low and
highly erratic
10
Horn of Africa; there is a lot of rifting activity further south as well, extending into
Kenya and Tanzania and Great Lakes region of Africa.
Figure 1.10 Rift segment names for the East African Rift System. Smaller segments are
sometimes given their own names, and the names given to the main rift segments change
depending on the source. (Makris & Ginzburg, 1987, Simon, 2010)
11
Summary
Many arid and semi-arid grazing ecosystems are not at equilibrium and external
factors (e.g. rainfall) determine livestock numbers and vegetation status. The
productivity of rangelands is heterogeneous in space and variable overtime;
therefore it is critical that the livestock movement must respond to spatial
changes in feed availability. In uncertain environments fodder availability
fluctuates widely over time and space. Grass production may range from zero to
several tons per hectare, depending on rainfall. Such variation is spatially
differentiated with same areas showing more stable patterns of primary
production while others are highly unstable. Making use of such variable fodder
resource requires tracking. Tracking involves the matching of available feed
supply with animal numbers at a particular site. This is opportunistic
management. Opportunistic management involves seizing opportunities when
and where they exist and thus highly flexible and responsive. Effective tracking
may be achieved in four ways: Increasing locally available fodder by importing
feed from elsewhere or by enhancing fodder production, especially drought feed
through investment in key resource site. Moving animals to areas where fodder is
available, reducing animal feed intake during drought, reducing parasite burdens
or breeding for animals with low basal metabolic (Larege animals) rates.
Destocking animals through sales during drought and then restocking when
fodder is available after drought.
Ethiopia has sufficient water in the western part and rivers in the vast lands of
the east, thus an alternative is the use of irrigated agriculture to boost crop or
fodder production. However, most of the range land soil is salt affected, 11
million hectares of land in Ethiopia are salt affected (saline, saline sodic and
sodic). The salt affected soils are a challenge to agricultural production. In the
Middle Awash Valley eight years after an irrigation project was commenced
salinity became very severe. Many productive agricultural lands were abandoned
and became barren land due to lack of appropriate irrigation water management
facilitated secondary salinization.
The drylands are rich in energy sources such as uranium, oil, gas and geothermal
power which are an as yet untapped potential treasure of wealth. Will these
bonanzas sustain the camel to be the king of the desert?
12
Figure 1.13 Livestock and cereal rotation in sedentary and pastoral interface
13
example, with some seasonal variations, still consume up to 59% of their diet as
milk or milk products with the balance of the diet being increasingly made up of
grain. For the Afar, milk probably constitutes less than 60% of total energy
requirements, and grain again is increasingly the main food substitute. This
increase of grain and decrease of milk consumption is in fact more and more the
pattern in pastoral Africa. Nevertheless the African pastoralist is still firmly
oriented towards a milk production mode as far as circumstances will allow and
has not yet dramatically changed this in favor of selling meat or growing crops.
Pastoralism relies on livestock diversity to exploit and make use of the diverse
rangeland resources, and typical pastoral herds and flocks include grazing cattle,
donkeys and sheep and browsing camels and goats. Pastoralism also relies on
diverse livestock products including milk, hides, meat, blood and draft power.
Camel pastoralism is most sustainable livestock production system in the drylands,
as the dromedary is a livestock species uniquely adapted to hot and arid
environments. It is also highly versatile; it produces milk, meat, and work, in an
environment where no other livestock can survive.
Camel pastoralists are those populations whose livelihood is based largely on
camel production. Camel keeping is their major occupation although at times they
diversify into keeping other livestock mainly sheep goat, cattle and sometimes
engage in agricultural operations. Their vocation is suited to exploitation of natural
resources. The main Ethnic groups and their herd composition are shown in Table
1.2
Table 1.2 Location and size of livestock in pastoral areas of Ethiopia (,000)*
Pastoral region (Location in Sheep Goat Cattle donkeys Camel
Ethiopia)
Horses
and
mules
2000
3000 3600
200
900
2 Somali (Eastern)
6600
3300 5200
360
1100
3 Oromo/Borena (South
Eastern)
Oromo/Kereyou(South
Eastern)
1000
500
1400
60
530
200
300
300
20
10
100
100
20
500
450
40
150
200
10
14
Figure 1.14: Camel Belt area of Ethiopia (Tefera and Gebreab 2001)
15
16
17
18
Drought time
Zone 1:
Dubti,
Asayta and
Afambo
Subzones
Zone 2
Awassa: close
Awash river
Zone 3 and 5
East and west of
the Awash river
south
of
the
Kombolcha Mile
road
Zone 4 and chifra
to
Western parts of
Yallo, Gulina, Ewa
and Mille subzones
Close to Awash
river
Amhara region
(Cheffa valley)
and Argoba
Oromia Zone of
Amhara region
close to Awash
river and Teru
19
Table 1.4: Wet and dry season grazing pattern in Somali Region
Zone
Wet Season
Dry Season
Gode
Foot hills and uplands
Along the Wabishebele river
Afder
Cheerti, Dolloban, Baren, Hargelle, Along
Genale,
Web,
Gorobagagsa
Wabishebelle rivers, El Har,
Yabow, Dhan Adir, Shakissa,
Budhi, Bali Baako, Qorsadula,
Gerar Elgojo, Qundi, Goroba,
Gagsa
Fiq
Qubi, Dooya, Dargamo, Qaruaqod and Gebre Abood, Digiweyne, Jajale,
Maymuliqa
Afmeer, Birqod, Malayko, Sulul,
Ela Sibi, Qarri
Deghabur Jig, Boholole, Dayr, Dig, Sibi
Fafan, Jerer, Galaisha, Dakhata,
Sibi
Jijiga
Babile, Gursum, Karamara
Jerer, Fafan Dakhata Valley
Qorehey
Jool Jeeh, Nusdaaring, Handheer, Bank, Gabagabo, Mariaado, Subaarco,
Dhobweyn , Kalajeen, Hannan, Har-Ano, El Har, Giid, Guoglo, Subauke,
Jiracle, El-Ogaden, Melka Afweyn, Shey Hoosn, Alla Gadwene,
Qorjeeh, Mario Ado, Elhaar, Banka Higloley,
Quruh,
Jeehdin,
Qoraheey, Banka Shaykosh
Herweyn
Liben
Ayinile, Gunway, Walenso, Moyale, Seru, Sora, Dinbi, and along
Wayamo,Chianqo,
Biyoley,Biyaoley, Dawa and Genale rivers
Boqolmayo,
Triyangolo,
Jarso
Dhafabulaale extensive grazing areas far
away from rivers birkas and ellas
Shinile
Hils and uplands
Araq, Bisiq, Muli, Qandaras, Erer
river and Somaliland
Warder
Laheelow, Dhurwa, Hararaf, Aado,Qorile, Wasdhug, Garlogubay, Yuub,
Darafole, Markha, Lifo, Agaarweywe, Uband Taale, Warder, Galadi,
Danod, Burawo and Las Anod in Somali Walwal
land
(Source: PFE, IIRR and DF. 2010)
20
21
During this normal stage pastoralists try to build up their herds, vary the
composition of their herds, and build up social networks. Strong ties mean
they can rely on others to help them during time of trouble. Crops can be
grown to supplement their diet.
2) Alert or Alarm stage: The rains fail and the early signs of drought appear.
During this time efforts concentrate on mitigating the effects of drought by
migrating to distant grazing reserves, concentrating around water sources,
selling extra animals, and giving gifts to relatives.
3) Emergency stage: Food and water run short causing severe malnutrition and
high death toll of livestock and the peoples efforts shift to relief measures. At
this stage people skip meals to reduce amount of food consumed, they
harvest wild plants, hunt wild animals, sell fuel wood and appeal to
government and donors for help.
4) Recovery stage: The rains return and people and animals can begin recovery.
Reconstruction activities are set in motion. During this period they rebuild
their herds.
There is overlap between these stages. Some particularly vulunerable people feel
the effects of drought sooner than others. Not all droughts go through all four
stages. Adequate preparations during normal and alert stages may prevent the
worst effect. Clearly, these droughts also affect natural resources. The amount of
available food decreases and water points dry up. But in most of the drylands the
vegetation shows a remarkable capacity for regeneration once rains return. Herds
can build up rapidly by grazing on fresh vegetation.
Pastoralist and crop farmers do different things at aach stage in the cycle and in
different places. What they do depends on the availability of other sources of food
and income, local traditions and the skills of individuals and households.
In general pastoralism can respond more easily and quickly to drought than can
crop farmers. They can buy or sell animals or move to new areas in search of water
and grazing. Crop farmers are tied to their land and must wait for several months
before crop is ready for harvesting.
22
Drought
Abandon Pastoralism
23
camels which they ride and use as work animals in mills and for ploughing. Such
traditional use is absent in the eastern part of Ethiopia.
Figure 1.18:
Kunama women
Figure 1.19
Kunama men
24
25
1.10.2 Irob
The Irob people also spelled Erob are an ethnic group who occupy a predominantly
highland, mountainous area in northeastern Tigray Region, Ethiopia. In general,
the Irob are a bi-cultural community, they are Christians and Muslim. Their
language is Saho and Tigrigna. The Irob economy is primarily based on agriculture,
including animal husbandry. The region is also renowned for its excellent honey.
Irobs raise camels; mainly male camel acquired from the Afar which they use in
trade such as wood and charcoal.
26
27
about daily life and general situations they observe, listen, or see on their ways or
from their areas of residence or from markets.
28
1.10.5 Somali
Somali: are ethnic groups located in the Horn of Africa, also known as the Somali
Peninsula. The Somalis speak the Somali language, which is part of the Cushitic
branch of the Afro-Asiatic language family. Ethnic Somalis number around 15-17
million and are principally concentrated in Somalia (more than 9 million) and in
Ethiopia (4.6 million) The name "Somali" is, derived from the words soo and maal,
which together mean "go and milk" a reference to the ubiquitous pastoralism of
the Somali people.
1.10.6 Borana
The Borana or Borena are part of a very much larger group of the Oromo culture
group. The Borana predominantly live in Ethiopia and Kenya. The economy and
life style are organized around cattle, though the formerly taboo camels are
becoming more important, and they now herd sheep and goats. Young men do
the daily herding while the women do all family nurturing. The homestead groups
may be required to move three or four times each year, often as far as 100 km,
because of the low rainfall and poor land.
29
1.10.7 Kereyou
The Kereyou are pastoralist nomads. Their tribe plies the arid lands around the
Awash River down in the rift valley for pasture for their cattle, goats and camels.
Their range area is located in the rift valley and Eastern Showa areas. They are
camel breeders, in addition they keep other livestock and recently they are shifting
to cultivate cereals and vegetables.
30
31
32
33
evenly while maintaining the productivity of the animals. The strategy also
guarantees continued provision of milk for settled families. When surplus milk is
available, it is sold in settlements to provide cash income for other family needs.
Thus, the strategy responds to both the needs of the camel and those of the
family. In this way the management of the herd ensures a sustainable flow of
benefits from the camels to the households while coping with production
constraints.
A study on the behavioral preference and quality selected forage by camels
(Dereje, 2005.) was conducted in the Erer valley of Somali region, with an altitude
of between 1300 and 1600m above sea level, to determine the behavior, dietary
preference and forage quality of free ranging dromedary. The vegetation cover
includes dwarf shrubs such as Indigofera species, large shrubs and trees such as
Acacia and Boscia species and is also highly populated by cacti. The annual
precipitation is between 400-500mm. The study was conducted both in the dry
and wet season and for different age and sex groups, i.e. young female, young
male, adult males and adult females.
Browsing and grazing was the dominant activity during the day (about 65% of the
10.5 to 12.5 hours per day they are outside the corral) in both seasons. During the
dry season the time devoted to browsing was significantly longer and in general
young animals spent more time browsing than adults. The study also looked at the
browsing preference of camels both in the dry and wet season. The camels
selected a total of 21 species of plants in the dry season and 30 in the wet season.
On average 79 and 83 percent of the camels diet was comprised of perennial
woody plants in the dry and wet season respectively. The difference in behavioral
activities within seasons seemed to be attributed to age differences. Young camels,
especially in the dry season, were observed facing difficulties eating thorny plants
such as Opunta and dry twigs, which leads them to spend more time on selecting
smaller and more delicate parts of plants to meet their nutritional requirements.
Camels were also seen to favor flowers and fruits when available. It was also
observed that camels did not eat from a single plant for a long time; instead they
moved around and took small portions from each plant, causing a low browsing
pressure on each plant.
The researchers recorded the ten most preferred plant species that occupied 87
percent and 80 percent of the total feeding time in the dry and wet season
respectively (Table 2.1.). Opuntia (18 percent) was the highest ranked plant in the
dry season, while Acacia brevispica (22 percent) was the highest ranked plant in
the wet season. The high water content of Opuntia may be the reason for its
34
popularity in the dry season. The A. brevispica had the highest CP content, both in
the wet and dry season.
Table 2.1 Forage plant species preferred by dromedary camels during the dry and wet
seasons.
Vernacular name
(Somali)
Dry season
Tin
Iswadh
Qudaahtol
Gidirmaan
Timirlog
Adaad
Keddi
Qalqalcha
Dhigrii
Dhigriaas
Merodimakaraan
Kalijog
Anannoo
Eriaad
Others, unidentified.
Karfaaweyn
Jeee
Kediqus
Eriqurn
Warsaames
Awus
Wet Season
Iswadh
Qudaahtol
Galol
Midhayoo
Adaad
Gob
Scientific name
Proportion of time
spent feeding
Category
Opuntia sp.
Acacia brevispica
Plepharis Sponisa
Indigofera
oblongifolia
Canthium
bogosensis
Acacia Senegal
Balanitus
Aegyptiaca
Boscia angustifolia
Becium
filamentosum
Becium sp.
Acacia sp.
0.18
0.15
0.11
0.09
Shrub
Tree
Herb
Vine
0.07
Shrub
0.06
0.06
Shrub
Tree
0.06
0.05
Tree
Shrub
0.05
0.02
0.02
0.01
0.01
0.01
0.01
0.01
0.01
0.01
0.01
Shrub
Shrub
Tree
Shrub
Shrub
Mixed
Shrub
Shrub
Tree
Shrub
Shrub
0.01
Grass
0.22
0.12
0.09
0.08
0.06
0.05
Tree
Herb
Tree
Tree
Shrub
Tree
Euphorbia tirucalli
Lantana camara
Boscia cariaca
Balanitus glabra
Vepris glomerata
Dichrostochys
cinerea
Mixed grass sp
Acacia brevispica
Plepharis Sponisa
Acacia bussei
Acacia melifera
Acacia Senegal
Ziziphus
35
Dhabi
Tin
Maran
Gidirmaan
Others, unidentified.
Keddi
Jeee
Eriqurn
Qalqalcha
Dhigrii
Merodimakaraan
Anannoo
Awus
Cekaa
Kabbaw
Futawadher
Timirlog
Hiil
Warsaames
Kalojog
Qarfaawein
Kediqus
Dhigriaas
Eriaad
mauritanea
Grewia tembensis
Opuntia sp.
Caucanthus edulis
Indigofera
oblongifolia
Balanitus
Aegyptiaca
Boscia cariaca
Vepris glomerata
Boscia angustifolia
Becium
filamentosum
Acacia sp.
Euphorbia tirucalli
Mixed grass sp
Calpurnia aurea
Commiphora
africana
Canthium
bogosensis
Vernonia
cinerances
Dichrostochys
cinaerea
Lantana camara
Balanitus glabra
Becium sp.
0.05
0.04
0.04
Tree
Shrub
Tree
0.04
Vine
0.02
0.02
Mixed
Tree
0.02
0.01
0.01
0.01
Tree
Shrub
Tree
Shrub
0.01
0.01
0.01
0.01
0.01
Shrub
Shrub
Grass
Shrub
Tree
0.01
0.01
Shrub
Shrub
0.01
Shrub
0.01
Shrub
0.004
0.004
0.004
0.004
0.003
Tree
Shrub
Tree
Shrub
Shrub
36
provides 95-99% in dry season, 90-97 in wet season. The rest is grazing, except in
dry season, fallow and residues each contribute 0.5%.
Acacia senegal, depending on soils and rainfall varies from a bush to a 10m high
tree, especially if heavily browsed by camels becomes a dwarf tree. Cactus
(Opuntia), O. ficusindica is especially in the dry season regarded outstanding dryseason camel fodder by the Somali. Cordia sinensis was rated by camel owners the
no.2 camel browse in Turkana District of Kenya.
Probably all Acacia spp. are browsed at one time or other by stock; Studies have
found, however, that in some regions even the camel, an animal with a reputation
for eating almost any plant, will shun some acacias. In Ethiopia, the species most
valuable for livestock are A. nilotica, A. senegal, A. seyal, A. sieberiana, A. tortilis
and perhaps A. mellifera and Faidherbia albida. All have palatable browse and
moreover nutritious pods that can be very important for camels. Singled out as
preferred or important camel food in the literature are A. drepanolobium, A.
oerfota and perhaps A. reficiens. In NE Ethiopia, Kahurananga (n.d.) found that
acacias formed the largest part of the camel diet; all species were browsed but the
most important were A. asak, A. mellifera, A. oerfota and A. Senegal, and A. tortilis
pods were considered excellent in camel milk production. The importance of A.
tortilis as a forage resource has been recognized by the Southern Ranehland
Development Unit (SORDU) project, and it encourages multiplication, and fencing
of seedlings.
Studies in the Borana rangelands indicated that there are about 15 woody plant
spp considered to be encroachers (OWWDSE, 2010). The major spp include
Commiphora afiricana, Acacia brevispica, Acacia nilotica, Acacia drepanolobium,
Acacia bussei and Acacia horida. A recent estimate indicated that about 52% of the
Borana rangeland is encroached by bushes and shrubs (Gemedo, 2004).
Livestock diet and palatability studies have recognized the importance of
commiphoras in camel and goat diets. The majority of the rangeland Burseraceae
is palatable to especially camel and shoats, even some of the sap-spraying species
appear to be good browse. Another obviously hedged species in this section is C.
truncata. It is an outstanding browse, the no.1 camel food plant according to
some Somali pastoralists. C. sphaerophylla (sec. Hemprichia) with its distinctly
sweet-smelling sap is almost its equal. Many members of sec. Opobalsameae are
highly rated but exhibit little or no browse impact. Among the boswellias, B.
microphylla and B. neglecta, both relatively large trees, are palatable and
outstanding feed sources for camel.
37
According to the pastoral area development study of 2004, browsing resources are
under-exploited, leaving ample space for the further expansion of camel rearing.
The study also mentioned that browsing animals have a much more environmentfriendly impact than grazing animals like cattle, sheep and donkeys.
The study on the behavioral preference and quality of selected forage by camels
(Moges, 2005) also collected feed samples of the ten most preferred species (Table
2.2.) in the dry season as well as the wet season were collected, dried and
analyzed using standard methods. All chemically analyzed samples had relatively
high crude protein levels. In both seasons, based on analysis of the ten most
38
consumed plants, the average diet consisted of 170g CP/kg dry matter, which is
similar to the amount required by high producing dairy cows. The range and
composition of the ten most preferred species (g/kg dry matter (DM)) were for
crude protein (CP) 88-228, P 1.3-3.3, Ca 12-48, soluble tannins 29-216 and
condensed tannins 9.4-129 absorbance unit/g. In vitro dry matter digestibility
(IVDMD) varied between 0.41 and 0.65.
The Ca: P ratios in the plant species are all very high, ranging from 6 to 16 in the
dry season and from 4 to 29g/kg DM in the wet season. Based on the chemical
analysis A. brevispica has the highest CP level in both seasons, while Opuntia has
the highest IVDMD level in both seasons. The results also indicate the high level of
tolerance of camels to the ingestion of tanniniferous plants
2.2 Feeding of Camels
Lactating dromedary camels on range in the Erer valley of eastern Ethiopia
substantially increased milk yield when supplemented with protein or energy feeds
(Dereje, 2005). Their experiment revealed that camels showed a good response to
supplementation with both CP (groundnut cake) and energy (maize), but with a
higher response to protein.
Feeding 4kg of groundnut cake daily per head improved not only the milk yield, but
also the net income by 88% in the dry season and 71% in the wet season. A higher
milk yield could reduce the competition between the calves and the family for milk
and thus increase calf survival. In turn this will have a positive effect on overall
herd productivity. Oil seed by-products in the region may thus have an important
role to play in improving the economic base of sedentary camel herders.
It is well known that anti-nutritional factors such as tannins from range plants have
a negative effect on nutrient availability, particular proteins (Kumar and
Vaithiyanathan, 1990) and therefore in this experiment it is possible that there was
a substantial increase in amino-acid uptake by the camels from protein
supplementation (groundnut cake).
39
Table 2.2: Composition (g/kg dry matter) and in vitro dry matter digestibility of the ten
most preferred plant species by camels
Vernacular
name
(Somali)
Dry season
Tin
Iswadh
Qudaahtol
Gidirmaan
Timirlog
Adaad
Keddi
Qalqalcha
Dhigrii
Dhigriaas
Dry season
Iswadh
Scientific
name
DM
Ash
OM
CP
Ca
IVDMD
TS
TC
Opuntia sp.
Acacia
brevispica
Plepharis
Sponisa
Indigofera
oblongifolia
Canthium
bogosensis
Acacia
Senegal
Balanitus
Aegyptiaca
Boscia
angustifolia
Becium
filamentosum
Becium sp.
213
725
173
80
827
920
133
214
2.6
2.3
38
21
0.654
0.486
144
110
9.4
28.9
777
127
873
126
2.4
39
0.453
55
13.8
207
157
843
150
2.1
28
0.498
51
12.7
666
72
928
165
2.2
18
0.469
146
83.1
517
111
889
191
2.2
25
0.491
80
22.2
263
81
919
200
2.4
15
0.497
78
17.7
405
115
885
206
2.4
22
0.507
110
22.7
646
86
914
160
2.6
25
0.457
113
30.8
713
80
920
165
2.4
25
0.450
110
26.7
923
228
2.3
23
0.512
128
29.9
847
131
1.6
46
0.484
46
14.8
935
930
199
116
2.4
1.7
12
21
0.481
0.467
216
76
56.9
29.2
942
180
2.1
14
0.538
147
27.4
936
189
3.3
14
0.599
44
39.2
909
171
2.1
26
0.491
178
129.0
845
921
88
201
2.4
1.3
32
27
0.619
0.408
119
138
22.8
38.4
802
218
2.4
48
0.610
29
11.4
Acacia
420 77
brevispica
Qudaahtol
Plepharis
256 153
Sponisa
Galol
Acacia bussei
344 65
Midhayoo
Acacia
261 70
melifera
Adaad
Acacia
374 58
Senegal
Gob
Ziziphus
172 64
mauritanea
Dhabi
Grewia
386 91
tembensis
Tin
Opuntia sp.
72
155
Maran
Caucanthus
401 79
edulis
Gidirmaan
Indigofera
138 198
oblongifolia
Tc= tannins condensed ts = tanisis soluble
40
DM: dry matter, OM: organic matter, CP crude protein, IVDMD: In vitro dry matter
digestibility, Tannins condensed: absorbance units/g dry matter.
Table adopted from M. Dereje, P.Uden / animal feed science and technology 121
(2005) 297-308.
Table 2.3 Effects of supplement treatment and season on milk yield and milk composition
and economic evaluation of diet supplementation.
Dry Season
Wet Season
Contro
l
Energy
supplemen
t
Production
Milk
6.9
8.6
(kg/Day)
Fat (g/l)
36
37
Protein (g/l)
26
27
Economic evaluation Costs
Supplement n/a
6.2
s
Other/dc
6
6
Income
Milk
17.25
21.5
Net
11.25
9.3
Protein
supplemen
t
Contro
l
Energy
supplemen
t
Protein
supplemen
t
12.2
8.2
9.5
13.6
39
26
38
28
37
27
39
28
3.4
n/a
6.2
3.4
30.5
21.1
16.4
10.4
19.0
6.8
27.2
17.8
41
importance of salt for camels is common knowledge among camel herders. In the
study area, camels depend on salt plants (halophytes), salty soils (kuro) and
sometimes commercial salt supplements for their mineral needs. Most herders
(70%) claim to follow a regular deficiency preventive routine. Camels kept in the
home-based herd were more frequently supplemented with purchased salt. This
was attributed to the fact that they had limited access to distant grazing areas with
salt plants. Salt deficiency symptoms revealed by the herders included chewing
bones, eating soils from anthills, reduced milk yield, reduced water intake, and
increased straying in search of salty plants.
Periodic salt supplementation was reportedly done once or twice a year in Somalia
(Elmi, 1989) and six to seven times in Kenya (Ayuko, 1985). Mineral deficiency can
cause a high susceptibility to skin disease (Dioli and Stimmelmayr, 1992; Bornstein,
1995) and consequently affects production. In addition, there are risks of loss or
predation when animals stray or break out of night enclosures in search of salty
plants. Camels manifesting bone chewing (pica), an indication of poor mineral
nutrition, was reported by 98% of the respondents. Further, 81% of the
respondents claimed to have seen their calves born with bent or weak legs, which
recovered later in life. A possible reason for the calf-hood defects is the insufficient
concentration of calcium and phosphorus in the bone matrices (rickets) in calves
from deficient dams. This suggests that mineral deficiency is widespread, posing
constraints to the performance of camels.
In the Afar Aba-Ala there is salt feeding proactice to lactating camels. The camels
respond to salt feeding calls from about 500 meters, they voraciously consume the
salt each camel was supplemented about 100g/camel/ day. Also seasonally
camels were sent to a place called Dergha a sort of special soil where animals were
able to lick mineral on voluntary basis. Its content was not dermined. Salt
supplementation was known to increase milk production. Sodium facilitates the
absorbtion of propionate a precursor of lactose in the rumen and also increases
water intake which inturn increases milk yield. Animals had access to water based
on groups, pregnant camels and males were watered every eight days. Lactating
came every other day and those at the end of lactation everty 5 days.
2.4 Water supply to camels
Water is by far the most important nutrient and an indispensable necessity for the
camel and livestock. The camel is highly resistant to water deprivation it can loose
upto 20% of its body weight and drink upto 200 liters in 20 min. However, the
ablity of the camel to withsand water deprivation should not be over exploited for
production puropses. It is necessity and must be provided on daily basis if water is
42
43
44
Appendix Table 21: Palatability of the different woody species for livestock species
Plant species
Grewia bicolor
Commiphora
Africana
Vernonia
phillipsiae
Dobera glabra
Dichrostachys
cinerea
Solanum
Vernacular name
Haroressa
Hamessa
Palatability
Highly palatable
Intermediate
Livestock species
Goat and camel
Goat and camel
Qexxee
Highly palatable
Adee
Germie
Unpalatable
Intermediate
unpalatable
unpalatable
Intermediate
Intermediate
unpalatable
Serritee
Acacia horrida
Acacia reficens
Allophylus
Chirree
45
abyssinicus
Borassus
aethiopum
Rhus natalensis
Dodonia viscosa
Acokathera
schimperi
Acacia
drepanolobium
Acacia bussi
Olea Africana
Cordia gharaf
Cocumis ficifolius
Grewia ferruginea
Grewia tembensis
Premna resinosa
Rytigynia neglecta
Lennae triphylla
Acacia albida
Borassus
aethiopium
Heeria reticulala
Ficus ovata
Croton
macrostachys
Commiphora
species
Ipomoe
hildebrandtii
(Commiphora)
Duranta repens
Calpurnia
subdecandra
Qalqalcha
Unpalatable
Xaxeessa
Itacha
Rukessa
Qararuu
Highly palatable
Unpalatable
Intermediate
Unpalatable
Intermediate
Qachachluu
Highly palatable
Intermediate
Intermediate
Highly palatable
Intermediate
Highly palatable
Highly palatable
Intermediate
Unpalatable
Intermediate
Intermediate
Dabobessa
Biqqa
Garri
Dembii
Mokonessa
Highly palatable
Highly palatable
Intermediate
Highly palatable
Unpalatable
Ejersa
Menayera
Guurbi hola
Dhogonuu
Deeka
Urgessa
Mudduguree
Andrakaa
Garbicha
Intermediate
Caalanqaa (sanga Intermediate
ajii
Omboorkeee
Intermediate
Sanaejo
Fonqolcha
Hammerrssa
Cheekata
Intermediate
Unpalatable
Unpalatable
Unpalatable
Miessa
Intermediate
46
47
Source of water
Rain water
Ground water
River
Spring
Ponds
Shallw well
Lake
Deep well
Reservoir
Tube well
48
49
herds specifying the animal breed, age, sex and usage. Reproduction and
production parameters are also available from the analysis (ILCA 1992).
The following list of six broad categories of breed descriptors were used
1. General identification consisting of country (region) species, breed or
population and location within the country the where breed is found.
2. Physical characteristics including coat color, giving details of special colors and
color combinations.
3. Measures of adult size and weight including wither height, live weight, and
body length (for each sex) with anindication of the precision of records, and
their standard deviation and range.
4. Current uses (purposes) as indicated by producers and ranked by priority.
Possession of special or unique adaptive traits such as resistance to major
diseases and to climate
5. Qualitative description of the predominant management system (stationary,
transhumant, nomadic, housing, feeding etc)
6. Biological performance important traits applicable to dairy, meat or dualpurpose breeds, giving an indication of variation.
3.1.1 Breed classification based on location
Each tribe and clan is a closed system of relationship all social activity takes within
the clan. Similarly for the camel as a clan may share a camel bull for breeding and
herds of camels may be exchanged and given as gifts. Although the external
features of the camel are not distinct, sometimes camels are classified by their
locality (See Fig. 3.1-3.3), for example the Kunama camel, the Afar camel,
theSomali Camel, the Borena camel, and the Kereyou camel. However, the Irob,
Kunama and Raya obtain camels from the Afar, usually males that are used for
transporting merchandise.
3.1.2 Breed classification based on color
The Kunama camel has a distinct whitish colouration unlike that of Afar and Somali
camels which is robably due to its origin from North Africa via Egypt. The Afar
camels are darker while the Somali camels are an intermediate golden brown.
However a mix of lighter and darker animals may occur in tribal herds. Color is
affected by age and younger animals tend to be darker. Classification based on
color is misleading. Darker camels are considered low producing but they may
possess other beneficial traits of survival.
3.1.3 Breed classification based on size
The Kunama camels are larger and taller while the Afar camels are lighter and
Somali camels are intermediate. Size is affected by age, sex, and plane of nutrition.
As there has never been an on-station evaluation, size can be misleading. In the
50
same herd it is possible to see different sizes of animals and seasonal body
condition fluctuations.
3.1.4 Morphometric measurement
Some relevant measurements were used to assess the phenotypic appearance of
the Afar and Somali camels. The mean heights of male and female camels were
1.89m, and 1.82m, respectively. The average mature weight of male camels ranged
between 350-500 kg and of females between 350-450kg under traditional system
of management. The mean weight of newly-born calves was 33.69 kg. Somali
camels were taller as shown on Table 3.1 with ashoulder height of 1.96 m. and
weight of 486 kg.
3.1.5 Breed classification based on production performance
Milk, meat and work performances are used for selection of breeding animals. The
trait most selected for is milk production and related characteristics are posture
and size of udder and mammary gland and pedigree. Three types of camels are
identified based on milk production, high yielding up to 10 litres, intermediate 7-5
litres and low yielding 4-3 litres per day. Female animals are never used for work as
the associated stress may hinder reproduction. Except for breeding bulls all males
are used as pack animals after they are trained to fit into a line caravan at age 5.
As it is difficult to differentiate camel breed based on external appearance, a tribal
herd of camels may be branded with an identification mark to show to which tribe
they belong. Moreover, variation in breeding success between males is a main
source of phenotypic selection pressure. No female is culled. In camel only the bull
is selected for breeding and practically any female camel is bread.
Over the last decades, advances in DNA-based marker technology make it possible
to identify genome regions, namely quantitative trait loci (QTL) underlying complex
traits such as milk yield in dairy cattle. Instead of traditional animal breeding
programmes solely relying on phenotype and pedigree information, the
incorporation of detected QTL into genetic evaluation provides a great potential to
enhance selection accuracies, hence expediting the genetic improvement of
animal productivity. The most important traits of dairy cattle are expressed only in
females, but the main opportunity for selection is in males. Intense selection of the
best bulls, combined with the worldwide use of these bulls through artificial
insemination and frozen semen, has created a global population and caused
concern that the genetic variation available in the future will be reduced.
51
Figure 3.1 Afar camel the reddish brown, lighter in color above and the
darker colored below
52
Figure 3.2: A herd of afar camels above and a Somali camel below
53
Figure 3.3: A female Somali camel, suckling its new born with
prominent mammary vein (above) and a two year old kunama
camel (below)
54
Table 3.1 Morphometric variables for Male Afar and Somali camels under pastoral
husbandry.
Morphometric
variables Mean (cm)
Neck length
Neck width
Hump height
Hump circumference
Tail length
Ear length
Chest width
Forelimb length
Hind limb length
Shoulder height
Thoracic girth
Abdominal girth
Afar*
Somali**
male
114.95
29.65
21.8
102.3
54.6
10.5
36.4
136.8
175.5
189.65
194.5
216
female
118
26
26.9
110.5
53.5
10.4
32.8
133.4
171.1
182.4
189.3
212.2
Male
female
1.96
2.04
2.52
Age
Weight
34
139
249.
273.
336.
376.
388.
421
470
500
55
56
57
3.2 Reproduction
Reproductive indices can be used as indicators of health, to measure responses to
treatment or control measures and as a guide to husbandry and management
practices. Ethiopian camels reach puberty at a relatively advanced aged, and
calving intervals are extended. The overall effect is that the parent herd grows very
slowly while the human population is growing at a higher rate. Seasonal
fluctuations of rainfall, watering frequency and drought cycles are directly related
to forage availability thus production and reproduction also fluctuate. For this
reason it has been difficult to exactly determine the maximum production and
reproduction potentials. Although the camel is capable of thriving in harsh
conditions provided there is good management, nutrition and health care
productivity is expected to increase.
3.2.1 Breeding behavior
Only one male camel, the alpha male (in Afar Shiden) manifests sexual activity
called rutt or math . A ratting male inflates a palatal flap as shown in Figure 3.5,
froths at the mouth, urinates back onto its body, does not eat and produces a
gurgling sound which induces sexual behavior . The camel bull or alpha male was
the largest and the strongest of the herd males and phermonally suppresses the
sexual appetite of other males, which undergo testicular atrophy. If this alpha
camel is removed thenthe sexual activity of the other males begins and fighting
occurs between them with the winer becoming the alpha bull. The breeders
themselves select a breeding bull and the criteria used are mainly body
conformation, color of the bull calf; milk production and pedigree of the dam. The
pastoralist detect heat in she camel symptomatically and hand mate it with a bull.
The she camel becomes restless, bleats when approached by the camel bull locally
known as Shiden or Koren.
3.2.2 Copulation
Copulation in camels, unlike other domestic animals which takes place in the
standng position, takes place in sittng position. The breeders assist the
coopultation by redirecting the penis for inexperienced bulls. If a female camel is
pregnant then she curls the tail up and refuses to breed as shown in Figure 3.5 . A
she camel in heat, will show flaping the tail, frequent urination vulval flipping and
accept for copulation when approached by a bull . Puberty in male camels occurs
at between 5 and 6 years of age. Mean rutting vigor in years for Ethiopian camel is
male Afar camel 7.85 0.51, with nine mountings per day and mean copulation
taking up to 7.31.46 minutes, (Tefera and Gebreab. 2001).
58
59
Figure 3.5: Sequence of copulation in the camel, right bottom picture shows a
pregnant camel manifested by tail lifting when approached by the bull
60
61
62
Parameter
Age at puberty (years)
Peak rutting vigor units?
Mountings / day
Refractory period unit?
Duration of copulation unit?
Reproductive span unit?
Male to female ratio
Age for castration Unit?
Seasonality
Mean
SD
4.8
7.85
9
40
7.3
11.5
1:150
5
Year round
Range
0.9
0.5
2
12
1.46
1.2
75
0.4
3-7
6-9
2-14
30-100
2-10
8-15
25-200
4-6
Reproductive parameter
Age at puberty (years)
Age at first calving (years)
Days to first service
Days open
Number of service per conception
Conception rate
Calving interval (months)
Calving rate
Gestation length Unit?
Reproductive span (Years)
Life time calf production
Length of gestation (days)
Dystokia Unit?
Seasonality
Mean
3.84
5
12
14
1.8
60
25.8
90
13
17
8
375.8
2
SD
Range
0.71
2-6
0.84
3-6
3.2
9-18
6
12-24
1-4
18
55-80
4.2
18-36
10
80-95
1.2
12-13
2
12-24
1
6-11
10.
365-395
1.2
2-8
Year
round
63
Male
Disease
Orchitis
Paraphimosis
Balantitis
Phimosis
Name in Afar
Beraa
Delle
Dhuh
Hayishowoso
Female
Disease
Metritis
Mastitis
Vaginal prolapse
Infertility
Repeat breeder
Anestrus
Abortion
Name in Afar
Ootcadabhintia
Due
Basur
Medelayto
Gerarta
Guhay
Bihay
Abortions
Stillbirths
Weaning age
Preweaning calf mortality
Post weaning calf mortality
Adult mortality per year
Mean%
Range
0.5
0.1
6
25
4
9
0-5
0-2
3-9
0-20
1-10
1-10
The calving interval varied from 18 to 36 months, and the mean calving interval
was found to be 25.804.2 months (Tefera and Gebreab 2001). Climate, feed and
need for milk was found to affect the calving interval. In drought areas, when
forage was scarce, maturity was delayed and first conception occured at a later
age. The Afar female camel can remain fertile to an age of 24 years and they
produce up to 12 calves but in pastoral production systems only a small number of
breeding females achieve this and the average life-time production was 8 calves,
and the mean reproductive span was 17 2 years, variying from 12 to 24 years.
The mean age at first calving 5 0.84 which varies slightly from place to place
according to Tefera and Gebreab, 2001 and Wilson, 1998 who reported 5 years,
and 4 year and 10 months, respectively. The relatively delayed age at first calving
in the camel could be attributed to the common practice of camel herders to
withhold females from breeding until they reached their nearly mature physical
size. Better feeding, improved health care and better overall management should
be implemented to enable camels to produce their first calf at younger age.
Female camels with calves were separated from the herd for milk, the females
being mated only a year after calving. An abortion or the death of the young
before weaning lead to a shorter lactation and calving interval than if the young
survive to weaning (Wilson, 1998). This was probably because lactation stopped
so the hormones controlling milk production which also suppress the reproduction
64
hormones disappeared and allowed animals to start their sexual cycles (Yagil,
1985).
3.2.4.5 Calf management
The calf is fed milk for 6 months. The importance of the presence of the calf on
milk letdown was well understood by camel herders (men) and in most
circumstances the calves were always present to iitiate milk letdown before
milking. At first the calf was brought near by the dam with no physical contact but
within the range of visual and auditory stimulation. If this failed to yield results
then the calf was brought into physical contact with the dam without suckling and
as a final option the calf was allowed to suckle for few seconds then the dam is
was milked. Only men were allowed to milk the camel. The calves were partially
weaned at about 6 months. The milk off-take rate is 50-75%, the pastoralist milk
two or three quarters and one quarter one or two quarters are left for the calf.
When a calf dies its skin is dried and the dummy is was shown to the camel during
every milking. Otherwise milk let down does not take place, and the lactation
would be shortened. The hide of the stuffed calf is salted so the dam licks it in
order to simulate the presence of the calf and enhance milk letdown (Hussien et al.
2008), as depicted on Figure 3.8 during milking or a bark made from special plant is
introduced in to the vagina of the dam so that it will be easily milked or foster feed
the orphan calf.
The calf mortality is very high. Most diseases like camel pox, pustular-dermatitis,
dermatomycosis, and camel mange affects the young. In comparison to other
animals, the camel calf has larger body surface area thus predisposing it to cold
stress (Schmidt-Nielsen, 1997).
Calves are housed separately form adults in a pen. Diseased calfs are also
separaeed. If the dam dies it is common to.
65
Figure 3.8: Housing of calves and traditional practice of managing she camel for
milking if the calf is dead
66
67
FAO-Addis Ababa
College of Veterinary Medicine, Haramaya University. P.O.Box 144 Haramaya
Campus. Ethiopia. 251-0914722459, melaku22@yahoo.com
2
The dromedary can survive and reproduce under harsh environmental conditions,
and still provide milk, transportation, draught and meat for its owners. The
available literature indicates that the carcass characteristics of camel meat are
generally comparable to those of other red meats, including beef, lamb and goat
and even of chicken (Alkahal, 1994).. Among the camel rearing pastoral
communities, the camel plays a key role in ensuring household food security. This
is because it is able to survive and remain productive in extreme weather and
fragile environments.
Interventions to enhance the production and productivity of camels and promote
use of appropriate technologies to add value to camel milk and meat leading to
increased marketing opportunities are designed to provide camel pastoralists and
key extension workers with the necessary skills and tools.
Camels are kept for the purposes of milk and meat production, transportation, to a
certain extent, traction and also for various other socioeconomic reasons, such as
rituals in Hajji, paying alms (Zeka) to the poor and cultural uses, such as dowries for
marriage (Wilson, 1989). The role of the camel is very important, as it is a more
versatile animal in such a fragile environment than any other livestock species. In
the Eastern region of Ethiopia, camel milk and meat are commonly consumed and
are sometimes preferred to those of cattle. Camel meat probably constitutes the
most important source of protein?? in the region, as it does elsewhere in arid
areas, such as Arab countries (Knoses, 1977). However, the potential of the
dromedary for producing meat and milk and its social and food values in the
pastoral areas of Ethiopia has received little attention
This chapter of the camel book aims to present a summary of the performance of
camel in production of meat, milk, and hide, and as a pack animal specifically in
Ethiopia.
4.1 Meat
Camel meat production represents about 0.7% of the world meat production, i.e.
216,315 tons (FAO, 2006), but information are quite difficult to collect as the main
part of the camel meat data comes from the informal market.
Camel meat has been eaten for centuries. It has been recorded by ancient Greek
writers as an available dish in ancient Persia at banquets, usually roasted whole.
The ancient Roman emperor Heliogabalus enjoyed camel's heel. Camel meat is
68
generally a common food item in Somalia, (where it is called Hilib geel), Ethiopia
Saudi Arabia, Egypt, Libya, Sudan, Kazakhstan and other arid regions where camel
meat has had a long cultural history.
According to the studies done by Kurtu (2004), the dromedary camel is a good
source of meat especially in areas where the climate adversely affects the
performance of other meat animals. This is because of its unique physiological
characteristics, including a great tolerance to high temperatures, solar radiation,
water scarcity, rough topography and poor vegetation.
In Ethiopia, camels are exclusively produced under traditional extensive systems
on poor levels of nutrition and are mostly slaughtered at older ages after a career
in work, or milk production. In the recent years, urbanization has increased the
camel meat demand in most of the country including in Addis Ababa due to the
increasing numbers of Somali inhabitants (personal observation).
A survey on camel meat productivity and consumption conducted in Jijiga and
Harar towns by Kurtu (2004) indicated that, the dressing percentage of eastern
Ethiopia camels was 54.035.13 for male camels and 50.653.70 for female
camels. Camel carcase weight was found to be 230.02 - 240.28 kg for males and
187.74 - 195.14 kg for females in Babilie, respectively, whereas in Kebribeyah it
was 214.77 - 225.03 kg for males and 199.76 - 207.16 kg for females.
4.1.2 Characteristics of camel meat
Camel carcasses contain about 57% muscle, 26% bone and 17% fat with fore
halves (cranial to rib 13) significantly heavier than the hind halves. The meat of a
camel up to 5 years of age is similar to beef, after which it may become tough
(Field, 2005). It has high water content, 22% protein and only 1% fat as this is
stored in the hump. Camel meat is low in cholesterol. The fat has a high melting
point and can be stored for at least a year without breakdown and smelling or
tasting unpleasant
Field (2005) reported that camel lean meat contains about 78% water, 19%
protein, 3% fat, and 1.2% ash with a small amount of intramuscular fat, which
renders it a healthy food for humans. Camel meat has been described as raspberry
red to dark brown in color and the fat of the camel is white in color. Camels
achieve a live weight of 350 kg in 6 years as shown on Figure 4. The dressing
percentage was 45%. The average price per kilogram in Afar was about 10 USD.
Camels were not slaughtered every day but only during special occasions when
one or two camels would be slaughtered in Asyta the capital city of Afar. Eighty
percent of slaughtered camels were old males, but sometimes, if a female gives
birth repeatedly to male calvesw then the calf is slaughtered to discourage the
dam from producing male calves. Slaughtering is mostly caied out on the floor and
the carcase is flayed from the back not from the belly as in other animals. Mostly
69
the slaughter method is halal in which the neck is severed at the thoracic junction
without prior stunning. There are no clear carcass cuts. The average price of an
adult camel ranges from 500-1000 USD, however, prices tend to fluctuate
according to seasonal demands, age and sex as shown in Table4.1.
4.1.3 Consumption
Camel meat is voraciously consumed in the region in second preference to mutton.
Camel hump and liver were the most preferred parts and may be eaten raw. Meat
is eaten either roasted or soup. Excess meat is dried in the sun and smoked. Table
4.1 Camel market prices
Table 4.1
Female
Price in USD
Male
Price in USD
700
Calf
600
Heifer 3-4y
1000
bullock
1000
Adult
1500
bull
1500
baggager
6000
70
The main problems and constraints associated with camel meat, as identified by
the consumers, is toughness and some undesirable favors, especially for an
occasional consumer. The general opinion is that camel meat is tough. This may be
due to age, since almost all the camels are aged when slaughtered. Elqasim and
colleagues (1987) stated that the meat of young camels (below 3 years of age) is
generally comparable in taste and texture to beef.
4.1.5 Meat preservation
According to works of Kurtu, M.Y. (2004) in Kebribeyah reported that it stayed
unspoiled and safe for consumption for more than one year. The findings of a
similar study, conducted by Tezera (1998) in Jijiga confirm that olobe (Dried
meat)can be consumed safely for more than one year
Table 4.2: Mean and standard errors of live carcass weights and dressing percentage of
dromedaries in Ethiopia.
Parameter
Males (n=88)
Live weight (kg)
46563
Carcass weight
25226
(kg)
Dressing %
545
**P<0.01 between male and female
Females(n=18)
33542
17020
Significance
**
**
503
NS
Parts of carcass
Males (n=88)
Hind quarter
Fore quarter
Neck
Hump
Longismus dorsi
Total meat
Red offal
Bones
Total carcass
Female (n=12)
Hind quarter
Fore quarter
Neck
Hump
Longismus dorsi
mean
SE
Weights (kg)
Minimum Maximum
47.2
76.0
13.5
33.5
24.7
195.0
10.0
47.0
252.3
12.0
11.8
3.5
7.7
4.8
39.3
1.5
2.6
44.5
35.2
64.1
10.0
25.7
19.7
154.9
6.1
44.8
206.0
59.0
87.0
17.0
41.2
29.5
233.5
11.3
50.0
296.0
36.0
45.8
10.3
19.8
14.3
10.3
8.9
2.9
5.8
3.79
25.4
36.9
7.3
14.0
10.4
46.3
54.7
13.3
24.9
18.0
Significance
**
**
**
**
**
**
**
**
**
71
Total meat
126.4
32.2
94.2
157.0
Red offal
6.2.0
1.3
5.7
10.1
Bones
37.5
3.03
36.8
46.0
Total carcass
170.1
42.9
127.0
213.00
** P<0.01 for difference between male and female (Kurtu, 2004)
4.2 Milk
4.2.1 Milk yields and lactation length
According Kuria et al 2005 study, It is difficult to estimate the daily yield of the
camel under pastoralist condition owing to the inconsistency of milking frequency.
Milk yield also varies with species, breed, stage of lactation, feeding and
management conditions. The length of lactation can vary from 9 t0 18 months,
depending on husbandry conditions which are largely determined by the need for
milk; more being required during the dry season than in the wet months when
other sources are available. Estimates of milk yield for different countries are
shown in Table 4.4.
Table 4.4 Camel milk yields reported from various countries
Country
Algeria
Ethiopia
India
Kenya
Pakistan
Somalia
Lactation length
(months)
9-16
12-18
18
11-16
16-18
9-18
Calculated annual
yield (kg)
1,460
1,825
2,482
1,643
2,920
1,825
72
The milk yield of camel varies greatly depending on the region and is a highly
debated one because of the conflicting data emanating from different regions of
the world. A peak total yield of 13,560 kg per lactation has been reported and a
single daily yield of as high as 50 litres a day has been reported from Northern
Kenya while camels in Tunisia yield milk of 2-4 kg a day during an 8 month lactation
period. The beauty with the camels is that they are capable of yielding more milk
than cows maintained at similar arid conditions in which camels yielded an average
of 4 litres of milk while cattle yielded 1-2 litres of milk. This reflects the potential of
camels as good dairy animals.
The lactation curve of camels is entirely different from that of other lactating
mammals because in cows the milk yield is low at the beginning of lactation and
gradually increases until a plateau is reached before declining. However, in camels,
it is high in the first seven months and then declines rapidly. The difference could
be due to poor management as well as milking practices. The milk yield of Bactrian
camels is low compared with that of the Dromedary.
In all pastoral systems the milking frequency ranged from 1-4 per day as depicted
in Figure 4.2, depending on the necessity and yield. The modal value was three and
milking times were 6am, 3pm and 6pm, with average yields of 5, 2.5 and 2 liters
respectively. The Afars believed three milking per day give a better yield than two
milking. The daily milk yield ranged from 0.5 to 8 liters with mean of 4.61.4 liters
per day. A maximum yield of up to 9 liters / milking was observed. The peak daily
yield was observed at 41.2 months post calving. The lactation length varied from
8-24 months and the most frequent lactation length was 15 months as shown in
Figure 4.3. Milk yield was estimated 1168-2190/year 3000l/ lactation. The camel
was milked in the standing position as shown in Figure 4.4. The importance of the
presence of the calf on milk letdown was well understood by camel men and in
73
most circumstance the calves were always present to imitate milk letdown before
milking. The off- take rate was75%, Otherwise milk ejection does not take place.
And the lactation would be short. Other factors that reduce the lactation period
were pregnancy and lack of food and water. When a she camel is pregnant milk
production is reduced. Primiparous camels had much lower milk yield and shorter
lactation than multiparous camels.
4.2.2 Milking process
The milking of camels is a process which varies according to the different pastoral
groups. In the Somali community camels may be milked once or several times a
day (personal observation). In general it is normal practice among most pastoral
communities to milk their camels in the early morning before animals are taken for
grazing and at evening when they return from grazing.
The milker stands on one leg, puts the milk pot on the upper part of the leg and
milks with one or two hands. Traditional hand milking is the only type of milking
used. Washing of udder and teats before milking is not practiced and the
producers believe that the teats get washed by the saliva of calf while suckling
Division of labor for milking is dependent on the species of animal: cows and goats
are milked by women, while milking of camels is commonly done by men. The
rapid let-down of milk in camels has been recognized by pastoralists who normally
milk with two people simultaneously, one on each side.
Traditionally calves are allowed to suckle their dams before (to initiate milk
letdown) and after milking (to drain whatever is left in the udder). Cows are milked
once or twice a day whereas camels are milked between one and six times a day
depending on the season.
Figure 4.4: Milking the camel and a child getting its meal
74
If a calf seems weak or becomes ill, its dam will be milked less frequently and the
amount of milk taken on each occasion will be reduced. In case of cow milking,
twice daily milking is a common practice in the wet season. However, milking
frequency decreases to once a day (in the evening) during the dry season (Table
10). Milking frequency in the area also depends on feed availability. Evening
milking in the dry season is practiced because cows are kept far from the
homestead for grazing during the daytime. Milk produced in the evening is kept in
properly washed and smoked utensils and marketed in the next morning (Hussien
et al. 2007).
In eastern Ethiopia, during dry times camel milk was the prime source of income to
the pastoralists, and camels contributed 59% to this source. There was an average
daily milk oftake of 3.6 and 6.5 kg from camels in the dry and wet seasons,
respectively (Baars, 1999).
Camels continue lactating during times of drought because water is not absorbed
from the mammary gland in order to conserve body water. In fact the milk
becomes more diluted, a phenomenon which is hormonally controlled (Yagil,
1988). The lack of drinking water increases the secretion of aldosetrone and
vasopressin, the hormones governing salt and water metabolism, leading to the
conservation of water and salt. This occurs when these hormones regulate
homeostasis but when they regulate homothermia, water is lost from the skin for
evaporative cooling. As the mammary glands have the same ontogeny as sweat
glands, the effect of vasopressin also causes water secretion into the mammary
glands, hence diluted milk. This phenomenon was also found in rats exposed to
heat and treated with vasopressin; instead of milk being concentrated it became
diluted (Etzon and Yagil, 1981). In addition, vasopressin in large concentrations
acts on the kidneys and mammary glands in the same way as oxytocin and vice
versa (Yagil, 1985). Therefore, dehydration leads to added water secretion and
hence protects milk volume while diluting milk. This is also the reason why
attempting to stop lactation by restricting drinking water in women or dogs fails
lactation continuesor is even enhanced. This finding was further reinforced by the
finding that diluted milk in cows was caused by increased vasopressin
concentrations when the animals were allowed only a fraction of the daily water
requirements (Yagil et al., 1986). Dehydration in camels leading to an increase in
salt content, thereby providing the calves with essential salt for metabolism.
These facts are important when considering using camels milk for various
products as the state of hydration will affect the composition of the milk and,
hence the product itself. Knoess et al. (1086), showed that camels were yielding
from 17 to 26 litres of milk per day and that after one year these volumes were
often unchanged or only slightly lowered (11 to 26 litres). Lactating camels still
maintained lactation capabilities after one-and- a- half years in spite of
75
Variable
Prefered milk type
Cow milk
Camel milk
Sheep milk
Goat milk
Consumption of Camel Milk
Number and
responses
proportion
1
2
3
4
76
(%)
of
Fresh
Sour
Mixed with other milk
100%
80%
13%
Most of the camel milk produced in Kenya is consumed at home, while only a small
portion is marketed. Among camel keeping pastoralists in Kenya, camel milk
constitutes almost 100% of total milk consumption in households during the dry
season and drought periods. A good example is among the Rendille pastoralists of
northern Kenya where camel milk provides 80% of the milk diet (Simpkin and
Guturo, 1995). During prolonged droughts, camel milk may contribute up to 50%
of total nutrient intake of some pastoralists groups
In Somalia camel milk is traditionally consumed either fresh or in the form of
fermented milk, known as Sussa. To prepare Sussa, the milk is left in a quiet
place, often in a covered container sheltered from dust for usually 2448 hours
until it becomes sour. The ambient temperature is normally between 25 and 35 C.
Due to the spontaneous nature of the fermentation, this traditional method
resulted in a product with varying taste and flavor and often of poor hygienic
quality.
Contrary to fermented milk, the manufacturing of butter and cheese from camel
milk is not a tradition in Somalia (Farah, 2003).
Camel milk is one of the most valuable food resources for the nomads in Sudan.
The milk is usually drunk fresh or when it has just turned sour. Traditionally, the
Sudanese camel owners consume milk in different forms, for instance fermented
or dried. The famous fermented camel milk in Sudan is called Gariss or Kashieb,
which is prepared in large skin bags or siin. Fermented camel milk or Gariss is
popular among the nomads in Sudan; it was first consumed by camel herders,
particularly in Gizu steppe land. Usually, two large skin bags full of fermented milk
(Gariss) are hung on to the saddle of a special camel (the Gariss camel). A few
seeds of black cumin and onion bulb are added to the Gariss skin bag for flavor.
The nomads, depending only on Gariss for long periods, also carry a lot of skin bags
of Gariss when crossing the desert during their routes to Egyptian camel markets
and when fetching salt as brine (Atron), from some hills in the middle of Libyan
desert. Faye, et al., (2011)
4.2.4 Characteristics of camel milk
The quality of camels milk is similar to that of a cow in many respects.
Fundamental differences, however, exist in butterfat, vitamin C, and protein
contents. The butterfat is lower in camel milk (3.7%) than in cows milk (5.7%) and
does not separate easily (Yagil, 1982). The milk is rich in vitamin C, ranging
between 5.7 and 9.8 mg/l or about three times the level in cows milk, probably
77
because of the kind of feed the camel is able to access. In the literature, you may
find other authors reporting a wider range of vitamin C in camel milk. This is very
important in ASAL (Arid and Semi Arid Lands) regions where fruits and vegetables
are not available as source of the vitamin to the pastoralists. The protein
lactoferrin in camel milk is about 10 times the content in cows milk. Protein
lactoferrin and vitamin C give camel milk strong medicinal properties against both
viral and bacterial diseases in human, e.g. diabetes, tuberculosis, stomach ulcers,
gastro-enteritis and cancer (Khler-Rollefson, 2000). A recent study in India
(Agrawa et al. 2002) has given scientific support to this belief. The Kenya Medical
Research Institute (KEMRI) in collaboration with the Kenya Camel Association is
currently testing the efficacy of camel milk in the management of diabetes in
humans in Kenya, comparing it with cows milk.
4.2.5 Camel milk preservation
As soon as production is higher than consumption, other ways of preserving and
marketing camels milk products must be found. Soured milk products are the
most common milk products of all mammals Smoking the container is the common
traditional preservation method and is practiced to improve the taste and the
quality of the milk. Moreover, it was noticed that only some selected plant species
are used to smoke the container because they were considered superior, and do
not affect or spoil both taste and odor of the milk (Ahmed Shiek 2010,
unpublished)
Soured milk
Souring of milk is practiced at any time when surplus milk is available and mainly
during wet season in a lactation period of 12 to 18 months.
Table 4.6 Traditional preservation tree species use to smoke camels milk vessels
Somali name
wigir
kidi
sogsog
Scientific name
Olea africana
Balanites galabra
Acacia ethaica
(Seifu, 2007)
78
4.2.6.1 Colostrum
Colostrum of camel is yellowish white in color and has a lower viscosity than that
of cattle. It contains high levels of total solids including total proteins, especially
the whey proteins and immunoglobulin. It also has high contents of ash and
chlorides, but low levels of lactose which are similar to bovine colostrum. Most
reports suggest that camel colostrum contains very low fat content when
compared to bovine colostrum which is rich in fat. Some differences between
colostrum composition of Dromedary and Bactrian camels are also noted, with
Bactrian colostrum being higher in lactose, protein, and ash content than that of
Dromedaries. (Khan & Iqbal,2001)
Casein, whey protein, and non-protein nitrogen represent 34, 57, and 9% of total
nitrogen respectively and these ratios are quite different from those of bovine
colostrum. Generally, non-protein nitrogen is higher in camel colostrum than in
that of cows, goats, and human colostrum. The mineral contents decreased with
progressing lactation. (Khan & Iqbal,2001)
4.2.6.2 Normal camel milk
Dromedary camel milk has a very white color and can be foamy and similar to
Bactrian camel milk. The taste of camel milk is usually sweet when camels are fed
with green fodder but sometimes it is salty when fed with certain shrubs and herbs
available in the arid regions. The physico-chemical parameters of camel milk given
in the above table vary widely depending on the country and factors such as type
of sample (individual or bulk), the analytical procedure used, lactation period,
breed of camel, feeding regimen etc. The total solids content is higher in Bactrian
camel milk than in Dromedary milk.
The effect of lack of drinking water on the composition of Dromedary camel milk
was studied and it was found that water content of milk changes greatly, although
the diet remained unchanged throughout the year. Water content of milk was 86
per cent when drinking water was freely accessible, but when drinking was
restricted, the water content of milk increased to 91%. This may explain why water
and total solids contents of camel milk in different data varied.
2.43
0.95
4.50
0.16
0.19
Libya
87.0
NA
NA
5.60
0.80 NA NA
NA
NA
Saudi
Arabia
87.7
1.90
0.90
4.78
0.83 6.50 NA
0.13
NA
Somalia
86.9
NA
NA
4.90
NA
NA
Ethiopia
85.6
NA
NA
3.40
0.90 NA NA
NA
NA
Kenya
87.7
2.64
NA
4.34
0.82 NA NA
NA
NA
Tunisia
87.9
2.88
NA
NA
0.16
0.20
India
90.2
NA
NA
4.20
0.17
NA
Pakistan 87.1
NA
NA
4.30
0.73 6.60 NA
0.14
NA
Figures given in the table are mean values arrived at from different sources; NA means Not Available
80
Figure 4.5: Skin lesions due to dermatomycosis rendering camel skin value less
81
82
Figure 4.7 Morning sene at salt quary at Danakil depression Afar (Sorce National Geography 2012)
83
Figure 4.8: Camel transporting household equipment above and in merchandise in towns
below
84
85
exports, of which 96% came from hides and skins. Thus commercialization
promotes agricultural and economic growth. The objective of this chapter is to
review commercialization of camel milk, meat and live animal value chains and
marketing structure in Ethiopia
5.1 Milk production and marketing
Camels are the most important signifier of wealth and determinant of status in
pastoral communities; their milk has been mostly used for domestic purposes. Sale
of milk was considered as Haram a taboo. However these days the sale of camel
milk is on the rise partly due to settlement of pastoralists and consumer demand
for camel milk, by economic factors and a break in traditional beliefs that selling
camel milk causes a decline in milk production of the herd. Camel milk is consumed
fresh and the main benefit is its high content of vitamin C which will be destroyed
if the milk is boiled. A camels lactating period is longer than a cows. Moreover,
camel milk is produced even under dry climatic condition. Camel milk has some
medicinal value, for example it is considered that the high content of selenium and
the amino-acid glutathione act as as immune boosters. In Ethiopia camel milk is
consumed by Muslims only and none of the Orthodox Christians use it.
Figure 5.1: Camel milk production in Africa (FAO, cited by SPORE, 2011)
In general the proportion of household milk utilization depends on a number of
variables including: accessibility of pastoralists to market; the numbers of milking
animals; the quantity of milk produced, and; the number of neighbors and relatives
that have insufficient numbers of milking animals. Seasonal and yearly climate
fluctuations also influence the proportion of household milk utilization and when
deciding what to do with the milk produced by their livestock, pastoralists have
several choices. Initially they must decide between:
i) Letting unweaned young animals consume all their dams milk, or;
86
Actor
Producer
Quality assurance
Retailer
Individual
Cooperatives
Whole sellers
Producers
Shops
Supermarkets
Hotels
Consumer
Role
Pricing
Figure 5.2: Actors in milk value chain market (Lumadede et al., 2010)
87
Milk marketing is traditionally done by women. The key actors involved in the milk
market chain are the producer, the trader and the consumer and all sectors are
dominated by women. Their organization is along kinship lines. Milk products
found in the market include fresh camel milk and fermented camel milk (Susac).
88
Milk is not processed except ghee made out of goat or cow milk. Camel milk is the
most preferred in Afar and Somali regions. It fetches the highest price and has the
highest turnover irrespective of the season.
5.3 Constraints of milk market
Some constraints to milk marketing are: poor infrastructure (roads, transport,
market buildings), and; especially the lack of cooling systems. There is no value
addition in the market chain, like pasteurizing, packing, churning. ASummary of
proposed intervention for the milk value chain are shown on Table 5.1
Table 5.1 Milk value chain improvement interventions
Proposed Intervention
Targeted audience
Impact
Training workshop on Producers, traders Improved
milk
quality,
improved hygiene
and consumers
increased sales of fresh milk
and increased income
Introduction of hygienic Producers, retailers
Reduced spoilage of milk,
milk
equipment
and
and increased income
handling
Milk testing practices
Producers, traders
Reduced adulteration of milk
Capacity
building
on Producers
and Increased income
buissness
management retailers
and marketing
Training on milk processing Producers retailers
Excess fresh milk can be
processed and stored
Improving
marketing Producers, retailers, Reduce spoilage of milk,
infrastructure, collection consumers,
local increase shelf life, leading to
points,
cooling
and authorities
improved public health
transporting
Strengthening link beween Prodiucers, retailers, Increased supply of milk,
market chain actors
transporters,
and stable market and prices
consumers
Lobbying with relevant National
and Improved policy environment
ministries for development Regional
to develop the dairy sector in
of the pastoral dairy Governments, Dairy the pastoralist areas and
industry
board, NGOs
formalizethe market
(Lumadede et al., 2010)
89
production. Guu is the main rain period from April to July when high milk yields are
expected. Hagaa is the cold and dry period from July to October again with lower
milk production and Deyr is the second main rainy season from October to
December with high milk production. The major milk production is in the rainy
seasons of Guu and Deyr. Despite the limited data, the trend for camels, cattle and
goats is the same and shows that the highest proportion of milk produced (6780%) by the three species is sold, while 20-33% is consumed at household level.
Milk yield per lactation is about 3,500 litres 25% is fed to the calf: pastoralists
manage this by leaving one quarter for the calf and offtake is 75% which means a
net yield of 2,625 litres, if 20% is consumed by household then 2100 liters can be
sold on the market at a price of 0.35 USD/ litre.
At producer level two thirds of the milk produced is sold, indicating that milk sale
contributes considerably to the household income. At the producer level the
average daily income during the dry season from milk sales is Birr 23.5, while it
almost triples during the rainy season to Birr 65.88. At the trader level the average
daily income does not vary much between the seasons and is some Birr 46.2
during the dry season as compared to Birr 44.75 during the rainy season. The
reason for this might be the producers increase their selling price during the dry
season by as compared to the rainy season and so the traders increase prices
proportionally Hence producers earn less income from milk sales during the dry
season, while traders can maintain their income by charging higher prices in the
dry season and benefitting from higher volumes during the rainy season. Milk is a
highly perishable commodity, especially under the high temperatures found in
Southern Ethiopia and milk spoilage is further compounded by long distances to
the market, which poses a challenge to the market chain especially the producers.
A requirement for effective marketing of milk is improved organization of the
producers and traders themselves. Currently, neither milk producers nor traders
are organized adequately for milk marketing. Thus a jerry can of milk that a woman
milk seller has in a market may contain milk from several households.
90
Milk
Fermented Milk
Fresh Milk
Cream
Consumption
Consumption
Market
Fed to calves
Churned
Market
Butter
Butter oil
(Remove
moisture)
Consumption
Consumptio
n
Market
Market
Market
Cottage
cheese
(Precipitate)
Consumption
Heat 50C
Whey
(Supernatant)
Fed to calves
This pooling of milk could, however, also lead to spoilage of milk, depending on the
health of the milked animals since no rigorous tests are carried out to enable
identification and isolation of bad milk. Improving hygiene standards at this level
will have a positive impact on the overall milk quality in the market (Lumadede et
al., 2010). This could include the joint procurement of cooling facilities such as
freezers and running of milk bars. Improving infrastructure is a key to the
improvement of the milk market chain. As it might be difficult to have an influence
on the improvement of roads, the simple introduction of strategically placed
collection points, e.g. using charcoal coolers or simple facilities with water and
cooling and the development of milk sheds and/or milk bars would contribute
positively to the improvement of the milk quality in the market. Currently these
structures are non existent and traders sell their milk sitting on the ground in the
market place. Awareness creation with line ministries and lobbying for the
91
92
93
94
5.7 Strength, Weakness, Opportunities and Threats (SWOT) of the meat sector in
Ethiopia
Internal Environment
Strengths
Weaknesses
Large livestock population
Subsistence production/ irregular
sales
Potential to increase productivity and
offtake
Land ownership problems
Potential for ranching and feedlots
Poor market infrastructure
Low labour cost
Poor road transport
Livestock and meat export firms
High transaction cost in marketing
channel
Plans for export zones and
certification
Illegal border trade
Export abattoirs*
Animal disase OIE list A
Multilateral and bilateral support
Poor veterinary services
Projects on fattening
Lack of value chain approach
Donner projects (USAID)
Obsolete slaughter equipment
Export promotion policy
Not oriented to wards quality and
consumer demand conscious
Foreign investment policy
Poor export facilities
Shortage of cooling/ freezing facilities
at the airport*)
Reliable of air transport
Strict financial export procedures
External Environment
Opportunities
High demand in the region (Middle
East and North Africa)
Relatively low sanitary requirements
(Middle East Market)
Potential cooperation with NGO
sector
EVD support (Netherlands)
Joint ventures
Threats
Import bans /Sanitary regulations
(Europian Markets)
Complication (Australia, NZ, Sudan)
Land locked country
Natural disaster (drought, famine,
conflicts)
*A warehouse with a special cooling unit for meat and carcasses has been inaugurated at
Addis Ababa airport and Mekelle (Nell, 2006).
95
Camel exports to Egypt flow through either Moyale to Nazareth to Djibouti and
Egypt or the Nazareth to Hamara (Ethiopia) or Sudan route. Sudanese traders
prefer the Djibouti route because it is less risky and camel deaths are fewer.
Camels from Moyale are preferred to those within Sudan due to breeed
preference and Sudanese traders are searching for cheaper animals elsewhere in
the region because camel prices in the Sudan have increased tremendously in
recent years, which has made their business tougher.
Camels are traded in small numbers along numerous markets, leaving the casual
observer with the impression that camels in a specific market are destined only for
local use. Additionally, unlike cattle or shoats that are transported on trucks, trade
camels are usually trekked on hoof through inaccessible paths to vehicles, far away
from the prying eyes of authorities. Camels bought from primary markets are not
immediately sold in terminal markets. They may be used as working animals or
conditioned to gain body weight at various transaction points for a year or more
before they are sold again.
96
Because of larger capital requirements, small traders are not able to buy more
than 50 camels at most at a time, compared to cattle and shoats traders who
usually buy hundreds of cattle or thousands of shoats.
Egypt consumes a significant amount of camel meat from Ethiopia, Eritrea and the
Sudan, Treands shows that Ethiopia is the preferred transit country for traders and
exporters dealing in Kenyan and Somali camels. The pricing, sales, and other
activities of the camel market in Moyale, Ethiopia are heavily dependent on
97
brokers. Sudanese traders in Moyale praise the role of their brokers for helping
them in the market place and reward them with some payment. Brokers are a
valuable link between Sudanese exporters and local pastoralists and sometimes
act as guarantors for both sides.
5.8 Structure of the livestock Supply markets
Livestock markets in Ethiopia function at three levels: primary, secondary and
terminal Markets (Solomon et. al. 2003.
Primary markets: village level markets, with generally less than 500 head of cattle
sold per week. Farmers and pastoralists sell animals to traders, other farmers
(replacement animals) and sometimes to consumers and local butchers. Generally
there are no facilities for weighing, watering and feeding.
Secondary markets: middlemen, trader and butcher dominated markets, with a
turnover of 500 1000 animals per week consisting of finished, breeding and
draught stocks and located mainly in regional capitals. Secondary markets serve
the local butchers and feed the terminal markets.
Terminal markets: located in the large urban centers. Medium to large-scale
traders dominate these markets. The supply of livestock to the primary, secondary
and terminal markets is mostly based on urgent needs for cash . Producers come
to the markets with no information beforehand on the going price of the day and
may take back their animals if the price offered is too low and l try their luck next
time at the same or another market.Livestock trading is subject to several service
fees and charges.
Figure
5.8:
Camel market
in
Somali
region
and
loading
for
export
98
Figure 5.8: Camel market in Somali region and loading for export
99
In Ethiopia, the pastoralist and agro-pastoralist areas such as Borena, Afar and
Somali are considered the traditional source of livestock supplying 95% of livestock
destined for export market (Belachew and Jemberu 2003).
5.10 Live animal and meat export value chains
The export market is relatively old but highly variable depending on production
condition of the country, changes in consumer preferences and greater demand
for high quality products with adequate guarantees of food safety (Ayele et al.
2003). The livestock market is structured so that the marketable livestock from the
major producing areas reach the final consumer or end user after passing through
complex channels along the supply chains involving various actors including
producers, middlemen, and livestock trading cooperatives, traders, live animal and
meat exporters. Market routes linking live animal and meat exporters with
secondary and primary markets, the generalized supply chains and marketing
channels for live animal and meat export are depicted in Figure 5. 8.
Value chain analysis is very effective in tracing product flows, showing the value
adding stages, identifying key actors and the relationships with other actors in the
100
chain (Schmitz 2005). Typically, a simple agricultural supply chain might include the
different market participants and their linkages, enabling business environment,
and business and extension service providers (Albu and Griffth 2005). The export
livestock marketing chain actors for cattle, shoat and camels are those who
transact a particular product as it moves along the chain from the primary
producers to the end users: producers, middlemen, traders, live animal and meat
exporters. The enabling factors for live animal and meat export market business
environment are the critical factors and trends that are shaping the market chain
environment and operating conditions which are generated by structures and
institutions (policies and regulations) that are beyond the direct control of the
market participants. Inputs and other services from other enterprises or service
provider organizations are provided for all the participants in the chain which will
allow the actors to grow and maintain their competitiveness in the supply chain.
Typically, a simple agricultural supply chain might include the different market
participants and their linkages, enabling business environment, and business and
extension service providers (Albu and Griffth 2005).
Figure.5.10: Meat production system in Ethiopia (M1= primary market; M2= Secondary
101
Most of the export abattoirs and live animal exporters collect animals either
through their own purchasing agent assigned in major livestock markets or
through other small- and large-scale traders. Sometimes livestock trading
cooperatives also directly supply animals to the exporters. Purchasing agents of
exporters in turn collect animals either from collectors, small traders, livestock
trading cooperatives, farmer groups or directly from producers. Producers have
the option of selling their animals to the collectors in their village, small traders,
and livestock trading cooperatives. Some farmers also form groups and supply
animals to the market. Other than the domestic channel, foreign national live
animal exporters-importers collect animals directly from the collectors in most of
the livestock markets using licensed Ethiopian traders. This channel is now
considered as the most rapidly expanding and competitive channel for the live
animal and meat exporters.
Figure 5.11: Factors vital in improvement of the camel market chain in Ethiopia
(Adapted from Mussa and Greenhalgh, 2007)
102
One of the special features of livestock marketing system in most livestock markets
is the involvement of brokers/middlemen in every segment of the marketing chain,
to match buyers and sellers and facilitate transactions. The volume of trade,
transaction costs, prices, and efficiency of the different market actors in each
channel requires detailed study. The roles of each of the livestock marketing chain
participants and a description of their relationship and transactions with other
participants in the chain are described below.
5.11 Market participants
Producers: These are pastoralists, semi-pastoralists and farmers producing shoats,
cattle and camels. Although these are the main source of marketed livestock, they
are located in the rural areas where access to the market is very difficult.
Marketing information for the producers is very scarce.
Collectors: These are important market agents collecting animals from their
locality and remote markets for supply usually to large and small-scale traders and
sometimes to livestock trading cooperatives. Collectors reach remote pastoral
areas around borders and collect animals in pastoralists temporary residences or
central watering points where they can find large number of producers. In most
cases, these actors are independent operators who use their local knowledge and
social relationships to collect animals from their surrounding and other remote
areas. To some extent, traders often place orders with trusted collectors.
Feedlot operators: Most of the feedlot operators are available at Adama and Dera
areas with their main role of fattening cattle for different markets. As part of
requirements of the Sanitary and Phytosanitary Agrement and according to the
rules and regulations of animal quarantine, fattening is carried out after providing
the cattle with the necessary vaccines and medication. But not camels.
Big traders: These are those market participants permanently operating in the live
animal and meat value chain and usually known by purchasing large numbers of
animals from different sources for supply to their customers. They are few in
number compared to small traders. One or two large traders are operating in a
certain area serving as agents for abattoirs.
Medium/small traders: Although medium traders are large in number relative to
large traders, the volume of their purchases is smaller than that of big traders.
Since they buy smaller number of animals at a time, they have very limited number
of collectors from the primary markets. Medium traders have smaller amounts of
operating capital as a result of which they collect limited number of animals on a
weekly or bi-weekly basis and transport them directly to abattoirs using rented
vehicles than waiting for the abattoirs trucks. In some other places like Borena,
these traders use abattoirs collection point as selling outlets. They also serve as
suppliers to the large traders in the secondary and terminal markets.
Medium/small-scale traders do not have strong trade relationships with specific
abattoirs. As a result, they do not have precise market information like that of
103
104
the terms particularly those in the higher end of the chain act only in their own
interests. This forces farmers who do not have countervailing economic power to
also act in their own price interests. Information about the the quality and quantity
of traded livestock which is demanded by the end-user does not properly filter
down to the lower ends of the chain. Conversely, information about livestock
production and associated cultural practices is not clearly understood at the higher
ends of the chain. There is no significant investment in the relationship; rather the
relationship in the market is based on mistrust. In this type of relationship, for the
most part, farmers are considered as input suppliers rather than strategic partners
in the value chains. The goal of the production system is only to satisfy producers
own requirements for cash, without giving much emphasis to meeting the market
demand and ensuring a sustainable supply of livestock to the market. This results
in unpredictable quantities and quality of products destined for different internal
and export markets and less remunerative prices for producers (Jabbar and Benin
2004). It also limits the development of value addition by various participants such
as producers, traders and processors.
As indicated above, market actors in the lower ends of the chain (producers and
collectors) are usually far from up-to-date market information. A practical example
in this regard is a misinformation about the export ban as a result of Rift Valley
fever reported in Kenya.
5.14 Market centres
Market centres and their associated infrastructures are important factors that
have to be considered in the move to increase the supply of livestock for both
domestic and export markets. Due to the wider geographical location of
pastoralists, some important sources of livestock are very far from market centres.
Pastoralists from the border areas need to travel for a week or more to reach
these market areas. This influences the marketing behaviour of pastoralists that
they either have to keep their animals unsold or they have to go to nearby
informal markets in the neighbouring countries.
The shift from subsistence dairying to commercial meat operations fundamentally
affects the pastoral community. A successful beef -or mutton- producing operation
requires a high survival of male stock; both heifer and bull calves must receive
adequate supplies of milk. For a pastoral community, raising bull calves on milk is a
luxury to be enjoyed only after human hunger is satisfied, and during the frequent
periods of low milk production male stock beyond herd reproductive requirements
may be allowed to starve. That is, in the hierarchy of milk consumers, pastoral children
in a subsistence dairy operation take precedence over animals. Shifting from
subsistence dairying to commercial meat production tends to reduce the size of the
pastoral livestock population. Commercialization can lead to displacement of labor
from poorer, subsistence-oriented pastoral households. This loss of a work force of
course further reduces the productivity capacity of poorer households
Population growth was the greatest challenge in the pastoral area as per capita
livestock holding had decreased from several hundred to a few animals. Due to the
105
above listed pressures the camel is disappearing from its former range and
reappearing in new areas. The reason why the camel appeared at higher altitudes was
partly due to new owners using the camel for packing as it is drought resistant and
partly due to an increase in the camel population. Nevertheless, the increase in
numbers of camel is not due to increased fertility but due to relative peace in Ethiopia
many Somali camel pastoralists were living inside Ethiopia (Tefera and Gebreab,
2001). Or, an increased trade-off as settlement was expanding creating a new habitat.
As former pastoral areas were converted to settlement, irrigated farms and parks the
camel pastoralists would be forced to browse their animal in remote areas and as a
result the camel has disappeared from its former range Afar camels reach puberty at a
relatively advanced age and the calving interval was 2 years. The overall effect of this
is that the parent herd is growing very slowly while a mere 2% offtake per year is a
stress to camels as they camel fertility is poor. Hence to improve productivity one has
to reduce mortality and increase fertility. Otherwise, it is like fishing the available
resource with no opportunity to regenerate.
On the other hand camel and other livestock export serve as a destocking gate which
improves the carrying capacity of the range.
106
107
Effective mechanism like taboo on selling animal and animal products was in place.
Moreover each pastoralist was not accumulating wealth other than livestock.
Exchange was through bartering, gifts and loans of animals and animal products.
With advent of monetizing pastoralism and expansion of markets in communal
land ownership, there will be a break in endogenous institution and culture Thus
maximizing individual share from the common property will increase resulting
ultimately in environmental degradation and lose of livelihood. Productivity per
hectare in the pastoral herd is very law. Thus the viability of pastoralism is a
challenge for policy makers. Credit can help herders replace livestock after
drought. The problems are mobility, unexpected risk of disease and draught and
lack of collateral for banking. Experts broadly agree that livestock production
needs to intensify and expand to keep up with population growth and meet the
increasing demand for meat and other livestock products But opinions diverge
about the how and how much. Between the two approaches, optimize production
processes and the use of locally available resources or change the system and
replace adapted strategies and labor with technology and energy.
108
109
110
of the time, but this should be for practical reasons (e.g. economic, cultural), and
not because you hadnt considered the Five Freedoms, and therefore all of the
ways in which welfare can be affected: Food and water, accommodation or living
conditions, the display of normal patterns of behaviour, treatment for disease or
injury, and the handling of the animal. Animal welfare is an important emerging
global issue, and the role of the veterinary profession has been identified as key
(OIE 2006). There is therefore a very worthwhile contribution to be made by vets
offering their skills on a voluntary basis in developing countries.
6.2 Duty care to camels
Whoever is in charge of an animal, he/she has a legal duty of care to that animal.
Being in charge of an animal usually means that you own it or have custody of it.
Having a duty of care to an animal means you are legally obliged to provide for its
needs by following certain welfare issues.
Anyone who owns manages or handles camels may have a legal duty of care and,
therefore, a responsibility to ensure acceptable welfare standards. This includes:
camel owners (commercial and non-commercial)
sale /yard agents
stock managers
veterinarians
stock handlers
processors
contractors
transporters
The basic behavioral, anatomical and physiological needs of camels are considered
in this code and comprise::
Water, food and air and salt to maintain health
Social contact with other camels
Sufficient individual clean dry space to stand, walk freely, lie down, escape
aggressors, stretch and groom
Protection from predation
Protection from disease
Protection from adverse effects of climate extremes or unusual changes in
weather conditions
Protection from unnecessary, unreasonable pain and suffering and injury
Water
A camels water requirement depends on age, body weight, disease status, level of
exercise, lactation status, temperature and dry matter content of feed eaten.
Camels should have daily access to water otherwise at least every other day.
111
Food
Camels are browsers and feed on trees, shrubs, bush and grasses.They prefer
plants with moisture and a high mineral content. In intensive farming camels
should be fed adiet containing 5-10 Kg of fibre each day. The feeding facility should
provide access to all camels. It is essential to provide licks containing salt, other
minerals and vitamins. They should be protected from poisonous plants.
Predation
Camels particularly young ones must be provided with adequate protection from
predators, such as hyenas, jackals and wolves and the Red-billed Oxpecker,
Buphagus erythrorhynchus.
Protection from climatic extremes
If housed there should be efficient ventilation, as camels lose heat by convection
and conduction, Housing must be well drained to permit the camels to sit down.
Protection from cold for non acclimatized camels and during transport should be
provided
Management
Handling: Patience and the use of positive rewards (positive reinforcement) in
handling the camel are effective. All camels are quick to learn good and bad
behavior and with experience to hat to avoid. Management practices that may
cause pain must not be carried out where a painless and practical method is
available. Restraint should be the minimum necessary to perform a given
management procedure efficiently. Any injury, illness or distress observed should
be treated promptly in any situation and a competent person must supervise.
Most camels are examined in sternal recumbency. Care should be taken to avoid
kicking and biting. When handling camels he first procedure should be to control
the head
Training
Camels should not be use for riding until 3 years of age. A four to five year camel is
considered as mature.
Load bearing
A camel should not be loaded with the maximum weight of 250 kg (for an adult)
until the age of seven years
112
Tethering
If a camel is to be tethered, the rope must be long enough to enable the camel to
lay down. Camels that are tied with short rope could strangle.
Hobbling
Hobbling for up to 12 hours or overnight is an acceptable husbandry procedure
provided that the camels are trained and hobbles are well constructed and used so
as to avoid pain and injury
Yard design
Height of race wall should be at least 1.8 m
Gate slide should be at least 2.4 m
Floors should not be slippery or abrasive
Yards should be designed without protruding objects that could cause injury
Cattle holding facilities are suitable for use with camels as long as they are
appropriately modified.
Castration
Surgical castration without general or local anesthesia is unacceptable
Castration must not be performed on calves
Nose pegging
It is recognized that nose-pegged camels are more effectively controlled than
haltered camels. Other methods of control of camels are the use of a rope halter,
nylon halter or chain halter. Those are preferable to nose peg on welfare grounds.
However they provide less control over the animal.. The decision to nose peg must
be based on the nature of the animal, the degree of training of the animal and
handler and level of control required. The nose peg is used as a steering aid and
not to restrain the camel. Once a camel is trained to sit down and stand up, only a
a light tug is required as the camel should respond to a voice command. The string
attached to the nose peg must be designed to beak in emergency it must not be
used as lead or pulled continuously as this may cause injury
Identification
A suitable method of permanent identification of camels needs to be developed.
Currently hot branding remains the only practical method and this is unacceptable.
Branding with corrosive materials is also unacceptable. Tattooing of the inner lip,
and plastic or metal ear tags are also suitable
113
Health
Camels should be treated for any ailment for which a remedy is available.
Prophylactic vaccines should be administered. Camels are extremely pain tolerant
and are sometimes reluctant to move if sick, thus they should not be beaten and
considered as malingering.
Transport
Camels dislike strange sounds during loading and transport. Camels of the same
size should be grouped together during loading. Bulls in rut should be penned
individually. Pregnant animals due to calve should not be transported as this may
cause abortion. Recently calved camels with suckling calves should be transported
together Animals should be fed and drink water before loading. Camels usually sit
down during transport there should be sufficient space for this. Seated camels
need to move their legs to stimulate blood flow and iff tied in the sitting position
must be allowed to stand every 4 hours. There should be adequate bedding.
Camels can be transported for a maximum of 3 days provided that feeding
watering and appropriate rest is given.
Euthanasia
If camels for some reason they have to be destroyed appropriate pharmacological
agents or physical method should be used. If the camel is to be slaughtered a
captive-bolt pistol should be used and once the animal collapses the major blood
vessels of the neck must immediately be severed.
114
(i.e. turned towards the tail) and the the main blood vessels in the neck, the
jugular vein and common carotid arteries, are severed with a single cut by a sharp
knife. Death occurs immediately. The Koran forbids stunning.
115
Halal: The great festival of Eid-ul Adha, is celebrated by the Muslims all over the
world every year through sacrifices and prayers in memory of the glorious sacrifice
of the prophets Ibrahim Khalilullah and Ismail Zabihullah (peace be upon them).
Thousands of camels are slaughtered on this auspicious day with a view to
receiving the Divine Mercy through benevolence, samaritanism, patience and
constancy. What is more, the Islamic practice of slaughter or sacrifice by slitting the
throat with a sharp knife has come under attack by some animal rights activists as
being an inhuman form of cruelty to animals. In Muslim countries the Islamic
method of slaughtering with a knife is considered to be the least painful and thus
the most humane method of killing an animal. In most of the Western countries, it
is required by law to first stun an animals to render itunconscious and thereby
preventing it from reviving before it is killed so as not to slow down the movement
of the processing line. It is also used from a humanitarian point of view. It is
presumed that this stunning prevents the animal from feeling pain before it dies.
Every year tens of thousands of animals die on the ships before they reach the
Middle East, and more succumb to illness and disease after arrival. These animals
may be the lucky ones. Most of them get injured, and many are trampled or gored
to death as they are thrown about in lorries that drive at breakneck speed. Also,
animals are tied together with ropes running through their pierced noses for
hundreds of kilometers, illegally crossing State borders by illegal traders. The
organisation Stop Live Exports is committed to ending the export of live animals
for slaughter. Stop Live Exports considers that animals ought to be slaughtered as
close as possible to where they were raised to avoid unnecessary suffering
116
Figure 6.3:
Abuse of camel
by overloading,
over working
and tracking
long distances
on track and
foot
117
118
researchers who made studies on camel respiratory diseases in Ethiopia agree that
Manhaemia haemolytica, Pasteurella multocida, Parainfluenza virus, and Morbillilike viruses are the major incriminated agents causing repeated outbreaks in the
country (Bekele, 1999; Fekadu et al., 2003; Rogers et al., 2001).
Various lower respiratory tract diseases have been reported in camels although
the definitive etiology of most respiratory diseases is not determined. A variety of
viruses have been associated with outbreaks of respiratory disease among camels.
Adenovirus (AdV), IBR viruses, influenza viruses A and B, PIV 3 and RSV were
identified so far in respiratory infections of camels (Dioli and Stimmelmary, 1992;
Intisar et al., 2009, 2010a, 2010b). Respiratory infections caused by AdV, PIV or
RSV may result in severe lower respiratory tract disease (Corne et al., 1999; Intisar
et al., 2010a; Trei, 2010).
The purpose of chapter 6 is to compile the most important bacterial, viral and
parasitic diseases that have been reported in Ethiopia and identify the gaps in the
study of camel diseases in the country.
7.1 Bacterial diseases
Camel respiratory diseases
The respiratory tract is continuously exposed to air that contains dusts, bacteria,
fungi, viruses and various noxious agents and to downward spread of the bacteria
which commonly colonize the nose and throat (Howard, 1993). Under normal
conditions the airways and the lung parenchyma prevent the entry of
microorganisms and neutralize or remove infectious agents so that the lung
contains very few, if any, organisms beyond the terminal lung units (Radostits et
al., 2007; Jones and Hunt, 1983). Hence, the effect of the infection here are more
severe and more ominous than in the upper respiratory tract (Jones et al., 1997).
However, the respiratory system has developed a series of effective measures to
counter against this. These complex protective mechanisms of the upper and
lower respiratory tracts are broadly categorized as physical defenses, cellular
defenses, and secretory defenses (Howard, 1993).
Respiratory diseases in food animals are due to a complex of factors that often
interact to produce disease. The management and environmental stress placed on
these animals are often the decisive factors between the development of clinical
diseases or the disease remaining sub clinical (Howard, 1993). Environmental and
management stresses like over-work, undue exposure to cold winds and rain,
sudden change of climate, insufficient food and chronic diseases, particularly
trypanosomosis, play an important role in disarming the respiratory defense
mechanisms through dehydration and increased level of circulating glucocorticoids
(Abdurahman and Bornstein, 1991; Dungworth, 1993; Andrews and Kennedy,
1997) as well as increasing in number and virulence of the agents (Radostits et al.,
2007). Once this normal pulmonary function is impaired or pulmonary tissues are
119
120
(Based on Ziehl Neelson staining). In addition three acid fast positive bacteria
(Mycobacterium spp) were obtained on Ziehl Neelson staining of three lung tissue
samples, while Mohammed (2011) identified a total of 37 bacterial species from 32
pneumonic lung samples collected from Oromia zone of Amhara regional state
(table 7.2). Also Ahmed (2010) conducted a study at Jijiga from October 2009 to
May 2010 to isolate and identify the bacterial species from lung of apparently
healthy camels slaughtered at Jijiga Municipality Abattoir and his findings showed
that coagulase negative staphylococci, Streptococcus pneumonae, Escherichia coli
and Mannheimia haemolytica were the most important bacteria inhabiting the
respiratory tract of camels (Table 7.2). The findings of the studies showed that
pathogenesis of respiratory diseases is complex and multifactorial and therefore,
these bacterial pathogens could themselves induce diseases or predispose camels
to other concurrent or opportunistic infections.
Table 7. 1: Prevalence of different pulmonary lesions encountered in lungs of camels
Lesion type
Prevalence
(%)
(Akaki, 2010)
60.2
21.2
18.6
10.6
4.9
3.9
and 2.6
Emphysema
Hydatidosis
Pneumonia
Atelectasis
Aspiration of blood
Pneumoconiosis
Pulmonary edema
congestion
Abscess
Pleurisy
Granulomatous pneumonia
1.6
1
0.8
Prevalence (%)
(Oromia
zone,
2011 )
49.14
22.41
35.34
6.03
16.38
12.93
0.86
Prevalence (%)
(Dire
Dawa,
2008)
30.80
34.62
-
6.89
9.48
-
3.85
50
-
1
2
3
4
Prevalence
Prevalence (%)
Prevalence
(%)
(Oromia zone, (%)
(Akaki, 2010) 2011 )
(Jigjiga, 2010
)
Staphylococci (Coagulase 21.1
48.7
tive)
Streptococcus spp
19.3
5.4
20.5
Escherichia coli
17.5
21.62
12.8
Francisella tularensis
5.3
=
121
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
Flavobacteria spp
Rhodococcus equi
Bordetella
bronchoseptica
Aeromonas hydrophila
Neisseria spp
Streptococcus agalactia
Staphylococcus auerus
Pasteurella trehalosi
Pasteurella anatipestifer
Pseudomonas aeruginosa
Micrococcus spp
Mycobacterium spp*
Klebsiella pneumoniae
Manhemia hemolytica
Actinomyces pyogens
Salmonella spp
Proteus species
Corynebacterium species
5.3
5.3
3.5
2.7
2.7
-
=
5.1
-
3.5
3.5
1.8
1.8
1.8
1.8
1.8
1.8
5.3
-
5.4
24.32
10.82
2.5
8.1
5.4
5.4
2.7
2.7
-
7.7
5.2
122
123
Figure 7.2: Histopathology of the lung [e: Acid fast bacteria on Ziehl Neelson
staining (arrow) (1000x), f: Hemorrhagic lymphadenitis distended sinus with
bloody exudates (arrow), g: Parafollicular hyperplasia of bronchial lymph node.
Expansion of T cell in parafollicular zone (arrow), h: Purulent lymphadenitis
Distended sinus with massive numbers ofneutrophils and macrophages (arrow)]
(Nesibu Ali)
Brucellosis
Brucellosis is a disease caused by various species of the genus Brucella which is the
most widely spread zoonosis worldwide (Dawood, 2008). The disease can affect
almost all domestic species and cross transmission can occur between cattle,
sheep, goat, camel and other species (Ghanem et al., 2009). These diseases have
great impact on economic development by affecting access to foreign markets,
124
apart from direct losses (morbidity and mortality) and indirect losses such as due
to the costs of treatment and control measures. Brucellosis has considerable public
health importance as owners (Abbas et al., 1987; Gameel et al., 1993) consume
raw camel milk. The prevalence is higher in intensive camel production systems
where large numbers of animals are kept in close proximity in a farm. In extensive
management system the prevalence is low (Abbas and Agab, 2002). Infected
animals show clinical signs of abortion and stillbirth in female and orchitis and
epididymitis in male animals and infertility in both sexes (Radostits et al., 2006;
Agab, 1997; Straten et al., 1997). In diversified production systems the disease
circulates in sheep, goats and cattle and further spreads to dromedaries (Andreani
et al., 1982; Radwan et al., 1992). Camels are not known to be the primary host for
any of Brucella organisms but they are susceptible to both B. abortus and B.
melitensis (Musa and Shigidi, 2001).
The studies conducted in Ethiopia to investigate brucellosis in camels showed that
the seroprevalence rate is generally low. Teshome et al. (2003) has reported 5.7
and 4.2% seroprevalence of brucellosis in camels kept in 3 arid and semi arid
regions of Ethiopia (Afar, Somali, Borana) using Rose Bengal Plate Test (RBPT) and
Complement Fixation Test (CFT), respectively. Teshome (2003) also reported 5.2%,
2.8% and 1.2 % seroprevalence from Afar, Somali and Borena which is statistically
significant (P<0.5). Omar et al., (2011) reported 1.6% overall seroprevalence of
brucellosis in Dire Dawa area is in agreement with the 1.8% seroprevalence in
Borena zone of southern Ethiopia by demonstrated Bekele (2004); 1.7% in Tigray
and 1.7% in Hararghe regions of Ethiopia by Domenech et al., (1977). Brucellosis in
camels has been reported in many countries showing different seroprevalences:
Saudi Arabia, 4.3-8.6% (Radwan et al., 1992); Egypt, 10-20% (Radwan et al.,
1992); Sudan, 4.9% (Abu Damir et al., 1984) and Somalia, 3.1% (Ghanem et al.,
2009). These varying reactor rates for camel brucellosis in different countries may
be due to varying husbandry and management practice, susceptibility of the
animal, virulence of the organisms, presence of the reactor animals in the region,
absence of veterinary service, lack of awareness by the nomads about the diseases
and the pastoralists movement from place to place.
Mastitis
Mastitis is an important camel disease, owing to its economic and public health
significance. As in other dairy animals, clinical mastitis in camel is self-evident and
can be detected without special tests by examination of the udder and milk.
Detection of sub-clinical mastitis is, however, difficult and depends on various test
procedures aimed at detecting Pathogens and indicators of inflammation in the
milk.
There are few studies concerning the etiology, occurrence and pathogenesis of
mastitis in Camelidae (Abdel Gadir et al. 2006). Recently, however, cases of
mastitis in camels have been reported from a number of camel keeping countries
125
including Somalia (Abdurahman et al., 1998), Sudan (Obied et al., 1996), Kenya
(Younan et al., 2001), Israel (Guliye et al. 2002) and from different parts of Ethiopia
(Almaw and Molla 2000; Woubit et al., 2001; Bekele and Molla 2001; Abdel Gadir
et al., 2006; Abera et al., 2010).
An intensive study of camel mastitis was conducted by Abera et al., (2010) in
Jigjiga and a total of 145 lactating camels were examined clinically as well as subclinically using mastitis test card with subsequent bacteriological examinations.
Clinical and sub-clinical mastitis were prevalent in 8.3% and 20.7% of the studied
animals, respectively. This gives an overall mastitis prevalence of 29.0% at animal
and 17.9% at quarter levels. The microbiological study of Abera et al., (2010)
showed that Gram positive cocci were the most dominant bacteria comprising
54.5% of the isolates followed by Staphylococcus species (49.1%), Bacillus species
(20.0%), Streptococcus species (5.5%) and E. coli (7.7%). Studies reported that tick
infestation and uses of anti-suckling device (tying the teat with tree fibers) to
prevent calves from suckling the dam are the major predisposing factors for the
occurrence of mastitis in camels.
The study of camel mastitis conducted by Woubit et al., (2001) found that the
major mastitis pathogens isolated were species of Staphylococcus, Streptococcus,
Micrococcus, Corynebacterium and Bacillus, and Actinomyces pyogenes,
Escherichia coli and Pasteurella haemolytica (Table 7.3). The result showed that
the more camels were affected by sub-clinical mastitis than clinical mastitis.
Figure 7.3:
Pictures
that show
lacerations
of the
udder
(Source:
Bekele
Megerssa)
126
Table 7. 3: Mastitis pathogens isolated from camels with clinical and subclinical
mastitis
Number of cases
Clinical
Mastitis pathogens
mastitis
Staphylococcus aureus
2
Staph. hyicus
1
Streptococcus
dysgalactiae
0
Strept. Agalactiae
2
Enterococcus faecalis
0
Strept. Uberis
0
Micrococcus spp.
0
Staph. intermedius
0
Staph. epidermidis
0
Corynebacterium
ulcerans
0
Corynebacterium bovis
0
Actinomyces pyogenes
0
Escherichia coli
0
Pasteurella haemolytica
0
Bacillus spp.
0
Total
5
(Source: Woubit et al., 2001)
Subclinical
mastitis
171
206
Total number
(%)
173 (21.1)
207 (25.3)
28
24
18
7
86
67
81
28 (3.4)
26 (3.2)
18 (2.2)
7 (0.9)
86 (10.5)
67 (8.2)
81 (9.9)
15
13
5
3
1
88
813
15 (1.8)
13 (1.6)
5 (0.6)
3 (0.4)
1 (0.1)
88 (10.8)
818
Tuberculosis
In pastoral communities of Afar, Somali and Borena, camels are kept almost
entirely for milk production. In these communities, camel milk is consumed raw,
and this habit combined with close physical contact with their animals create a
potential public health concern for transmission of zoonotic diseases such as
tuberculosis (TB) from animals to the pastoralist. Although, the extent of TB has
been well documented in humans and most domestic animals, very little is known
about the pathology and cause of camel TB in pastoral areas of the world. Camel
TB has been reported in Egypt, United Arab Emirates, Pakistan, and Australia
(Gezahegn et al., 2011). Mycobacterium tuberculosis (M. tuberculosis),
Mycobacterium bovis (M. bovis), and atypical mycobacteria such as
Mycobacterium kansasii (M. kansasii), Mycobacterium aquae (M. aquae),
127
Figure 7.4: Tuberculous lesions from camels in different organs (Source: Gezahegn
Mamo et al, 2011)
1) Disseminated and distinct tuberculous lesions in mediastinal parts of the lung.
(2) Tuberculous lesion in mediastinal lymph node and nodules on other parts as
128
indicated by arrows. (3) Tuberculous lesions in hepatic lymph node. The arrows
show that pea-sized lesions throughout the lymph node. (4) Tuberculous lesion in
mesenteric lymph nodes as indicated by arrow.
Anthrax
Camel anthrax is an acute or peracute disease caused by Bacillus anthracis. Bacillus
anthracis spores may remain viable in the ground for 60 years. Fazil (1977)
indicated that the disease in camels is similar to that in other species but Leese
(1969) is more specific, observing that camel anthrax is similar to the form
observed in horses and pigs. Major signs observed include oedematous swelling of
the head, throat, neck and body. Involvement of the throat may lead to difficult
breathing and swallowing. It is possible for death to occur without septicaemia,
and apoplectic and diarrhoeic forms may also be observed.
In Ethiopia, Richard (1976) reported serious outbreaks of anthrax in camels, with
some grazing areas being notorious for the disease. Bremaud (1969) wrote that
anthrax was particularly rampant in the Wajir camel herding area of eastern Kenya.
7.2 Viral diseases
Viral Respiratory Infection
Pulmonary diseases are among the emerging problems of camels that are causing
considerable loss in production and death (Zubair et al., 2004; Kane et al., 2005).
However, the definitive etiologies of most respiratory diseases of camels have not
yet been determined as a variety of viruses, fungi, bacteria and parasites are to be
the possible causes of respiratory outbreaks among camels (Schwartz and Dioli,
1992). Dioli and Stimmelmary (1992) reported that the viruses that have been
associated with respiratory infections in camels are Parainfluenza virus 3 (PIV3),
Influenza viruses A and B, adenovirus, respiratory syncytial virus (RSV) and bovine
herpes virus-1(BHV1).Various lower respiratory tract diseases have been reported
in camels, but the definitive etiology of most respiratory diseases is not
determined.
Most of the studies on camels were of parasitic infestations (Al-Rawashdeh et al.,
1999). Al-Tarazi (2001) and other authors had isolated and characterized many
bacterial agents from pneumonic camel lungs. However, there is little or no
information on possible viral etiologies of camel pneumonia or viral flora in camels
in Ethiopia. Recently a study was conducted from September 2010- June 2011 at
Debre Zeit National Veterinary Institute (NVI) in an attempt to isolate and
characterize respiratory viruses from pneumonic lungs of camels slaughtered at
Addis Ababa Akaki abattoir (Wossene, 2011). The study findings showed that out
of thirty five (35) pneumonic camel lungs that were cultured 27 were CPE- positive
characterized mainly by initial rounding of vero cells, elongation, syncytia
formation, swelling and rounding, floating and sloughing of cells (Table 7.4).
129
During the study period the involvement of respiratory syncytial virus and
adenovirus were confirmed as a causative agents for camel respiratory diseases.
Table 7.4 Summary of conventional PCR test results
No.
samples
tested
of
PCR Results
Positives
Adenovirus
Peste
des
virus(PPRV)
petits
ruminants
Negatives
10
Parainfluenza virus1(PIV1)
130
Most recently Fitsum (2011) conducted a PPR serological study in Afar areas and
found an overall prevalence rate of 13.7% in the study areas. The overall
seroprevalence rate reported in this study is higher than the previous findings from
Ethiopia where seropositivity of 7.8 % (Roger et al., 2001), 3% (Abraham et al.,
2005) and 1.5% (Megersa, 2010) were reported. The result is also higher than
other findings reported from Egypt with 4.2 % seroprevalence (Ismail et al., 1992)
and from Turkey (Albayrak and Gur, 2010) where all the camels tested where
seronegative. The result of current study is similar to the finding from Sudan with
14% seroprevalence (Haroun et al., 2002).
Camel Sudden Death Syndrome
In 2005/06 in Afar and Kereyu area in Oromia region, there was a huge camel
mortality which was characterized by sudden death (Wernery et al., 2006). Also in
2007 a similar syndrome was reported from Somali region and Guji and Borena
zones of Oromia. During the 2005/06 outbreak the Ministry of Agriculture and
Rural Development (MOARD) invited scientists from Plum Island Animal Disease
Centre, USA, and the Central Veterinary Research Laboratory (CVRL) of Dubai to
conduct disease investigations in collaboration with Ethiopian veterinarians from
the National Veterinary Institute (NVI), the National Animal Health Diagnosis and
Investigation Centre (NAHDIC) Sebeta, Regional Veterinary Laboratories. The team
attempted to identify the cause of the disease, but were unable to draw definitive
conclusions.. During this investigation the majority of the camels examined
(necropsy or serology) had parasites including haemonchosis, trypanosonosis,
tapeworms and other round worms and also bacteriologically different species of
bacteria were isolated such as E. coli, Clostridium perferenigens, Sterptococuss,
Enterobacter amnigenus, Bacillus cereus and others, but none of these is
pathogenic under normal condition, particularly for adult animals including camels.
The histopathological investigation revealed lymphoctic myocarditis, in some
instances combined with myocardial degeneration and necrosis which indicated
the presence of viral infection, but no virus was isolated. Virus isolation was also
attempted at the NVI and Plum Island facilities using different cell lines. Cytopathic
effect (CPE) was observed in vero cells, IBRS-2 and BHK cells. However, electron
microscopy and microarray studies were inconclusive and a viral agent has not yet
been identified.
131
Figure 7.5: Picture of a dead camel in Negelle area (Source; Gelagay Ayelet, 2007)
A similar camel disease was reported from Sudan in August 2004, clinically the
disease was characterized by sudden death of apparently healthy animals and
yellowish and later bloody diarrhea and abortion. The researchers conducted
several laboratory tests such as Agar gel diffusion test (AGDT), RT-PCR and virus
isolation in cell culture and reported that tests were positive for peste des petits
ruminants virus (PPRV), a virus belonging to the Morbillivirus genus, member of
the family Paramyxoviridae (Abdelmelik et al, 2010).
A similarly study was conducted at National Veterinary Institute by Dejene (2010)
on samples collected from Borena area during the 2007 camel sudden death
outbreaks with the aim of identifying viral agents. During this study virus isolation
was attempted in Vero and lines cells; four specimens yielded cytopathic virus
when inoculated onto the Vero cell culture. The cytopathic effect (CPE) consisted
of round floating cells, giant cells, rounded refractive cells, ballooning of cells,
sloughing, and some syncytia formation was observed from day two to day seven
post inoculation. The appearance of the CPE was similar among the different
purified tissue samples used for cell infection. The growth of virus was confirmed
by degenerate oligonucleotide primed PCR and RNA virus was detected, both from
tissue and cell culture. The isolated virus types confirmed to of the adenovirus,
morbillivirus, parainfluenza 1-3 and respiratory syncytial virus groups.
Pathogenicity studies on laboratory animals were conducted to determine the
132
progress of the disease under laboratory conditions in laboratory animals. For this
purpose 20 mice of 3-4 weeks of age and 20 adult guinea pigs were used. The
guinea pigs were showed depression, weakness, inappetance, erected and rough
hair, rise in body temperature as well as heart beat and fast and labored breathing
starting from the third day of inoculation onwards. The assay resulted in the death
of six guinea pigs 20 days post inoculation. The negative control animals also died
between 29 to 32 days post contact without showing any clinical signs of disease,
while the mice remain healthy throughout observation period. The finding showed
that guinea pig can serve as a model animal for further study.
Figure 7.6
The
cytopathic
effects (CPEs
of infected
vero cells
with camel
sudden
death
samples.
(Source;
Gelagay
Ayelet,)
Table 7.5 Growth of virus on two cell lines and amplification by DOP PCR from samples
collected during the sudden death outbreak.
Tissue
Growth
Growth
DNA
type
on Vero
on Dubca
tissue
culture
tissue
culture
lung
Nt
heart
++
++
liver
++
++
heart blood
++
++
lung
Nt
++
++
RNA
133
Camel Pox
Camel pox is a wide-spread infectious viral disease of both Old World and New
World camelids. It occurs throughout the camel-breeding areas of Africa, north of
the equator, the Middle East and Asia, causing economic impact through loss of
production and sometimes death. The disease is characterized by fever, local or
generalised pox lesions on the skin and in the mucous membranes of the mouth,
respiratory and digestive tracts. The clinical manifestations range from inapparent
infection to mild, moderate and, less commonly, severe systemic infection and
death. The disease occurs more frequently and more severely in young animals.
Transmission is by either direct contact between infected and susceptible animals
or indirect infection via a contaminated environment. The incubation period is
usually 913 days (varying between 3 and 15 days). Skin lesions appear 13 days
after the onset of fever, starting as erythematous macules, developing into
papules and vesicles, and later turning into pustules. Crusts develop on the
ruptured pustules. These lesions first appear on the head, eyelids, nostrils and the
margins of the ears. In severe cases the whole head may be swollen. Later, skin
lesions may extend to the neck, limbs, genitalia, mammary glands and perineum.
In the generalised form, pox lesions may cover the entire body. Skin lesions may
take up to 46 weeks to heal. In the systemic form of the disease, pox lesions can
be found in the mucous membranes of the mouth, respiratory and digestive tracts.
The Mortality due to camel pox is reported to range from 2% in the mild form, and
28% to 40% in the severe or systemic form (Abbas and Omer, 2005).
The only study of camel pox in Ethiopia was reported by Bekele Megerssa (2010) in
Borena area. His study was mainly based on observation and he reported the
occurrence of seasonal variation; 14.2%, 0.3% and ???% prevalence during minor
wet, major wet, and dry seasons respectively. This may be due to the fact that
moisture may enhance virus stability in the environment and increase subsequent
transmission to susceptible animal.
134
Figure 7.7: Pictures that show camel pox lesion (Source: Dr. Ulli. Wernery)
135
The occurrence of the disease in Ethiopia was reported by Bekele Megersa (2010)
in young calves with higher incidence rates during the wet seasons (16.0 21.2%)
than the dry period (1.4%). Such a seasonal pattern of occurrence of the disease
was also observed by Agab and Abbas (1999), with higher prevalence during the
rainy season.
Figure 7.8:
Megerssa)
136
Mange mite infection due to Sarcoptes scabiei var cameli was one of the most
commonly encountered camel diseases in Borana with severe clinical
manifestations. Sarcoptic mange infections were more prevalent and severe during
the dry periods. Moreover, the disease was more severe in young and female
animals (Tefera, 1985) transmission was common during suckling hence the head
of the young and genitalia of the female were the most infection sites. Prevalence
of over 50% was observed by Bekele Megersa (2010) who reported concomitant
infection with other diseases including contagious skin necrosis, abscess and
contagious ecthyma.
Camel mange, sacoptes scabi cameli is very difficult to detect in skin scrapings
boiled with 10% potassium hydroxide. One has to leave the sample in the boiled
solution for longer than 3 hours after boiling in order to to see the mange mites
under a microscope (Tefera, 1985).
137
Tick Infestations
Ticks are a major constraint on the worlds livestock industry. Ticks exert a major
hindrance to improving animal production in the tropical and subtropical regions
of the world by transmitting devastating and often fatal livestock diseases, causing
blood loss, damage to hides and udder, and paralysis (Zeleke and Bekele, 2004). In
Ethiopia, ticks and tick born diseases cause considerable losses to the livestock
economy, ranked third among the major parasitic diseases, after trypanosomosis
and endoparasitism (Pegram et al., 1981). Numerous studies have been
conducted on the ticks and tick-borne diseases of cattle and small ruminants in
Ethiopia, but work on camel ticks is scanty, despite the vital role that camels play
in the livelihood of Ethiopian nomadic society and the likely impact of ticks on their
productivity.
A study conducted by Zeleke and Bekele (2004) to identify the species of ticks
found on camels (Camelus dromedarius) and their seasonal population dynamics in
Eastern Ethiopia showed that the most abundant species of ticks on the camels
were Rhipicephalus pulchellus (85.2%), Hyalomma dromedarii (5.9%), Amblyomma
gemma (4.0%) and Amblyomma variegatum (1.8%). The average tick load per
camel was higher during rainy months than during dry months. The smallest
number of ticks per camel was observed during the driest month (December),
whereas the highest was recorded in the wettest month (August).
A similar study conducted by Bekele Megerssa (2010) in the Borena area revealed
that the pooled seasonally collected ticks belonged to the three genera, namely
Repicephalus (83.2%), Amblyoma (13.6%) and Hyaloma (1.2). The species
identified include R. pulchalus (77.5), R. eversi (18), Amblyoma gemma (13.4%),
Amblyoma vargatum, Amblyoma lipedum, Hyaloma dromedari. The tick Boophilus
is rarely found on camel (Tefera, 1985).
Gastrointestinal Tract Parasitic Diseases
Gastrointestinal helminths cause losses through morbidity and hidden effects on
feed intake, efficiency of nutrient utilisation and also reduce growth rate in young
animals and as a result lead to reduction in productivity and performance of the
infested animal. Rutagwende (1985) stated that dromedary helminthosis is the
third most important production constraint.
Several studies have been conducted in Ethiopia to determine the prevalence, type
of gastrointestinal tract (GIT) parasite in camel and to understand the seasonal
occurrence of the disease. Bekele (2002) conducted one study in the Jigjiga area
and found that of 752 dromedaries examined, 75% were infested by nematodes.
This indicates the extent of the problem in the dromedary rearing areas of eastern
arid lands of Ethiopia. Also Abebe (1991), Birhanu (1986), Melesse (1995) and
138
Bekele and Tezera (1998) has reported prevalence rates of 87.0, 91.5, 95.3, and
95.1%, respectively, from different camel rearing areas of the country.
On the basis of fecal (1,500 samples) and postmortem examination, Richard (1979)
estimated that 92% of the animals examined in various parts of Ethiopia were to
some degree infested with internal parasites (80% with Strongyles ova, 10% with
Strongyloides larvae and 16% with Trichuris ova). Fourteen helminth species were
identified on postmortem examination, the main ones being Monezia spp., Stilesia
vittata, Avitellina centripunctata, Trichuris globosus, Haemonchus contortus,
Trichostrongylus spp. and Impalaia somaliensis. Mixed infections with
Haemonchus sp., Trichuris sp., Cooperia sp. Nematodirus and Trichostrongylus sp.,
to name a few, are the most common. Bekele. (2002) examined sixteen
dromedary gastrointestinal organs for identification and counts of helminths.
Among the adult worms he identified in the abomasum, Haemonchus longistipes
was the most prevalent (94%). From the small intestine Trichostrongylus
colubriformis, Trichostrongylus probolurus, Impalaia tuberculata and Strongyloides
papillosus were identified with prevalence rates of 75, 25, 63 and 20%,
respectively. Moreover, cestodes such as Moniezia benedeni, Moniezia expansa,
Avitellina spp. and Stilesia globipunctata with prevalence rates of 31, 13, 25 and
19%, respectively, were identified.
Sarcocystiosis
A survey of sarcocystis was conducted in camels from southern Ethiopia in
1998/99 by M. Woldemeskel and B. Gumi who worked on a total of 605
haematoxylin and eosin-stained tissue samples from cardiac, diaphragm, shoulder,
masseter and oesophagus muscles of 121 adult camels and 20 tissue samples from
four fetuses. According to their findings sarcocysts were detected in 55 of 121
(45.45%) camels examined. The infestation rate of oesophagus, diaphragm,
shoulder, masseter and cardiac musculatures were 19.83, 11.57, 12.4, 8.26 and
9.17%, respectively. There was no signifcant (P > 0.05) variation between males
(48.6%) and females (40.82%), nor between the two sites studied (Dollo Addo, 40%
versus Negelle Borana 47.25%). None of the 20 tissue samples from the four
fetuses examined harboured sarcocysts.
Trypanosomosis
Among many diseases that affect camels in Ethiopia, trypanosomosis (Surra) is the
most important parasitic diseases (Richard, 1979; Getahun Demeke, 1998;
Thewodros Tekle and Getachew Abebe, 2001) The disease which is widely
distributed throughout camel rearing areas of the Somali, Oromiya (Borena) and
Afar regions (Figure 7.10 and causes considerable economic damage due to loss of
beasts of burden and food. The causative agent of surra (T. evansi) is unicellular
flagellated protozoan parasite belonging to the subgenus Trypanozoon.
139
Figure 7.10 Camel trypanosomosis areas based on parasitological data, NDVI and Tmax
Change (Getachew Abebe, 2005)
Due to the fact that the disease is characteristically found outside the tsetse belts,
it is considered that T. evansi is transmitted mechanically by biting flies such as
Tabanus and Stomoxys. The parasite is incapable of cyclical development in tsetse
fly because it lacks the genes needed for formation of the mitochondrion, which is
a prerequisite for cyclically transmitted members of the brucei groups (Hoare,
1972). The distribution of surra in Ethiopia coincides with the distribution of
camels, which is far away from the tsetse belts of the country.
The pathogenesis of T. evansi infection in camels varies according to the virulence
of the particular strain of parasite, the susceptibility of the host and the local
epidemiological conditions such as the presence of carrier animals and the vector
(Figure 7.11).
140
Figure 7.11: Transmission of Trypanosoma evansi in the presence of carrier animal and the
vector
141
Figure 7.12: Trypanosome infected camel with poor body condition (Source: Getachew
Abebe)
Figure 13: Trypanosoma evansi in camel blood smear (Source: Getachew Abebe)
142
The integration of camel husbandry into the traditional pastoral economy of the
Southern rangelands is a recent development. The Borena pastoralist who have
lost large number of cattle due to droughts have started to rely on camels as a
more reliable insurance against climatic calamities (Dessalegn Belete, 1984).
Because of limited available grazing lands it is common to see camels herded with
cattle and small ruminants. As a consequence, exposure to contagious diseases
and various endo- and ecto-parasites leads to high morbidity and mortality and
consequent restriction of herd growth and productivity. In realization of this fact, a
study was conducted to determine the prevalence of camel trypanosomosis and
helminthiasis in the southern rangelands of Borena, Ethiopia (Thewodros Tekle and
Getachew Abebe, 2001). Out of 391 blood samples examined 43 (10.9%) were
found to be positive for T. evansi. The disease caused by T. evansi infection is well
known to the breeders by the local name "Dhukane" and is given the first place in
its order of importance among camel diseases. Clinical signs observed in the acute
cases of the disease were hyper-lachrimation, rough hair coat, weakness and
depression. The camel owners also reported a sharp decline in milk production and
abortions in pregnant animals. Trypanosomes were observed in the blood smear of
the animals in the acute stageof the disease. In its chronic form camel owners
reported that the disease was manifested by emaciation, disappearance of the
hump, weakness and general loss of production, decreased milk production and
long calving interval.
Contrary to the parasitological findings, a large proportion of camels were showing
the clinical signs of trypanosomosis. The chronic nature of the disease and the
possible presence of trypanosomes in extravascular locations (Ngernawa et al.,
1993) might explain the difficulty in demonstrating trypanosomes in the blood of
chronically infected camels by the routine laboratory methods employed in this
study. Although blood examinations showed negative results, the response to
treatment resulted in improvement of the health of the camels as stated by the
breeders and this is taken as a good indication of the widespread presence of the
disease in its chronic form.
Balatidiosis
It is a GIT protozoal parasite of camel. Most
camels were infected with no symptoms
(Tefera, 1985).
Balantidium cameli was found in all 200 fecal
samples of camels examined by direct smear
in the Dire-Dawa clinic. The camels were
apparently healthy with no clinical sign. Fecal
samples revealed a ciliate protozoon,
Balantidium cameli. In 50% of the samples we
143
found only the ciliate, while in 24% there were ciliates and strongyle-type eggs.
The consistency of the feces of associated animals was viscous (Tefera, 1985).
No human were affected by it. The species could be opportunistic infection and its
pathogenecity should be determined in the future
Figure 7.14 Balantidia cameli
Cephalopinasis
The disease is caused by Cephalopina titillator, which is an obligate parasite of
camel, and the larvae of which cause nasal myiasis. The larvae infect the posterior
pharyngeal pouch and nasal mucosae of camels. Many investigators have reported
the occurrence of the disease in Ethiopia. Richard (1979), Tefera (1985) reported
that 100% of the Ethiopian camels are infected with C. titillator, in Borena and
Harar which is the highest prevalence rate ever reported in the country. Kassa
(1995) and Bekele (2001) reported that 99.3% and 71.7 % of camels at Dire Dawa
were harboring the larvae respectively.
144
145
146
147
Figure
7.17
Saddle
soure in
camel
148
149
In conclusion the health status of camel is very vital for the normal production and
productivity. Like other domestick animals camel suffer from different diseases of
bacterial, viral and parasitic origions in addition to physical trauma caused by
heavy loads of household assets and commercial goods. The heathcare of camels
and the extension packages are not well developed in Ethiopia due to the lack of
knowledge and skills in health delivery system. Particular emphasis should be
given to neonatal mortality not only affects the number young calves but also the
milk production.
150
151
152
innovations. At any rate it is important to note that research should also carried
out on experimental stations. The packages should then be adapted in light of
initial experience, while more intensive research on specific components, offering
favorable projects for improvement should also be launched. Once a promising
improvement package has been identified, it can be recommended for extension
on a wide scale, with due regard to transferability to systems in which camel are
raised. A coordinated multi-disciplinary approach would appear to be necessary
Research gaps and Research Strategies
General objectives of camel research
Reduction of vulnerability of pastoral communities by increasing security,
access to water and pasture
Increase productivity of the camel
Increase production for export
Development of pastoralist institutions
Increase income by taking a value chain approach to marketing
Rangeland improvement and alleviation of environmental degradation
Research strategy
1) Breed improvement
2) Husbandry improvement
3) Feed amelioration
4) Camel health
5) Camel product and by products
6) Pastoralist socio-economy
1. Breed Improvement
There is no information on the classification of camel breeds, low genetic
potentialand lack of genetic improvement programs
Strategy
Population census
Systematic identification of phenotypes
Molecular characterization
On-farm and on-station breed evaluations
Selection and cross breeding
Breeding technologies and alleviating infertilities
Key areas: Breed characterization, selection, breed registration, reproduction,
2. Husbandry improvements
153
154
155
5. Socioeconomy
The pastoral production system can be simply viewed from a systems perspective.
In this case the various pastoral economic, social and organizational structure are
viewed as integrated and complementary to each other, they function to ensure
the survival of entire system in which livestock is the productive capital. The
success of livestock rearing thus revolve around efficient labor organization,
respect for the functionally prescribed norms and value communication networks,
religious beliefs, gender role delineation, resource management need to be
investigated
Strategy
Study of endogenous knowledge
Study of migration patter of various clans
Study labor availability and division of labor
Gender roles
Land tenure regulations
Religion
Demography
Community interaction
Conflict resolution
Key areas: Migration, labor, tenure, Endogenous knowledge, conflict resolution,
demography,
B. Pastoralist fate scenario
The nomads in the past have suffered a paucity of infrastructure and social
services and hence isolation from the center which has limited their integration to
the national economy. Government policies with regard to pastoral economies
have tended to favor state control in the direction of confining pastoralist to
particular territorial boundaries. The rational has been to get them to settle down
for ease of administrative and security service for them. In 1950 the Awash Valley
Authority was established and resulted in expansion of irrigated agriculture by
state and private individuals. In the 1960s, the Livestock and Meat Board was
established with the task of developing water points, markets, veterinary services
and roads. In the 1990s large towns such as Asayata and the new Semera town
projects have transformed the socioeconomy of the pastoralists. Many pastoralists
were transformed intogovernment employees, traders, wage laborers. In addition
an inflow of highland farmers into pastoral/agropastoral areas and expansion of
opportunistic farmers to agropastoral areas resultedin the following:
a) Migration to marginal areas
b) Seizing new grazing areas
c) Becoming sedentary or semi nomadic farmers
156
Force of change
Commercialization of
pastoral production
Conservative opinion
It will change the
composition of the herd
in favor of cattle and
small ruminants.
Increase in marketing of
animals decreases the
number of animals for
traditional loans and
Reformist opinion
This trend is not harmful
to the pastoralist. It could
have selective advantage.
Livestock market is an
element of incorporation
of pastoral system into
force of
modernity.Improves the
157
Settlement
carrying capacity of
rangelands, herders can
pay medical and school fee
The reformist state the
thesis of Hardins tragedy
of the commons. Herders
seek to maximize their
personal gain by increasing
their herd size without
limit, until the common
grazing resource is
completely destroyed.
Hence destocking and
ranching are prescribed
Provided that pastoralists
are the beneficiaries and
obtain due compensation,
pastoral areas should not
for ever be reserved for
exclusive use by pastoral
groups because the valley
are fertile
Agropastoral has
advantage in terms of risk
spreading in areas where
there is enough moisture
and fertile soil
158
ANNEX
(Source : Tefera 1985)
Physiological triads of normal camels
Day time
Number of Animals
Morning (8H-10 H)
17
Afternoon (13H-15H)
16
36.5
35.7-37.4
38.9
37.5-38.9
11
9-16
11
9-16
Heart Rate
Mean
Range
45
35-50
45
40-50
Rectal temperature oC
Mean
Range
Mean
Range
Total RBC
Total WBC
Haemoglobing/dl
PCV%
RBC fragility
Maximum
Minimum
Differential count %
Neutrophil
Eosinphil
Basophil
Monocytees
Lymphocytes
7,000,000
14000
12
36
5,200,000 - 8,940,000
12000 - 16000
9 - 16
27 48
0.44 - 0.36
0.28 0.22
60
2.5
0.5
7
30
48 65
14
01
5 10
24 37
159
160
161
162
Restraining the camel in standing position. A, Foreleg ring tie and B, foreleg bend tie
163
164
Dental formula
(Source: FAO )
165
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
No teeth
No teeth
2 cheek teeth on each side
One cheek tooth on each side and 2 front teeth
1 canine , 3 cheek teeth on each side
3 front teeth, 1 canine 2 cheek teeth on each side
1 front, 1 canine, 3 cheek teeth on each side
3 front , 1 canine, 2 cheek teeth on each side
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Upper jaw
Lower jaw
Sign
166
Lankeyr
Abeskul
Weyten
Horona
Adali
Lateral thigh
Nose up to ear
Lateral abdomen
Lateral side neck
Lateral arm (L&R)
Abdomen
Lateral thigh
Helelacto
Hump to abdomen
Lateral neck
Infra orbital area ( L& R)
Afar Tribe
Mendita
Banturo
Geraysa
Hereke mela
All Afar
Nose
Lateral neck
Abdomen
Lateral abdomen
Lateral arm (R)
Lateral abdomen
Lateral side neck
Lateral abdomen
Lateral Arm
Lateral arm
Mange
Respiratory disease complex
Hemorrhagic septicemia
Clinical signs
Acute thinning of hump, promonent ribs, pale
mucous membrane, abortion
Papule, vesicles, pustule, scabs, swelling of the
head and lymph nodes, nasal and lachrymal
discharges
Pruritis, alopecia
Nasal discharge, grunting, mouth breathing
Swelling of lymph nodes, dyspnoea, tarry faces and
167
Cephalopsis
Camel pustular dermatititis
Dermatomycosis
Gastrointestinal parasites
Plant poisoning
red urine
Coughing by lowering the neck, circling
Wart like growth around the lips, in young animals
Alopecia, no itching, asbestos like crust
Poor body condition
Excessive salivation, paralysis of leg, grinding of
teeth
168
REFERENCES
Abbas, B. and Omer, O. H. 2005: Review of infectious diseases of the camel
Veterinary Bulletin 75(8), 1N 16N.
Abbas, B., and Agab, H. 2002: A review of camel brucellosis. Preventive
Veterinary Medicine 55, 47 56.
Abbas, B., El Zubeir A. E. A., Yassin, T. T. M. 1987: Survey for certain zoonotic
diseases in camels in Sudan. Revue de` Elevage et Medicine Veterinaire
des Pays Tropicaux 40 (3), 231-233.
Abdel Gadir, A. E., Hildebrandt, G., Kleer, J.N., Molla, B., Kyule, M.N., Baumann,
M.P. 2006: Comparison of California Mastitis Test, Somatic Cell Count
and Bacteriological Examinations for Detection of Camel (Camelus
dromedarius) Mastitis in Ethiopia. Berl Munch Tierarztl Woshenschr 119,
4549.
Abdurahman O., Agab, H., Abbas, B., and Aston, G. 1998: Relation between
udder infection and somatic cells in camel (Camelus dromedarius) milk.
Acta.Vet.Scand. 36, 424431.
Abdurahman, O. A. Sh. 2006: Udder health and milk quality among camels in
the Errer valley of eastern Ethiopia. Livestock Research for Rural
Development 18, 1-9.
Abebe, W. 1991: Traditional husbandry practices and major health problems of
camels in the Ogaden. Nomadic Peoples 29, 2131.
Abera M., Abdi, O., Abunna F., and Megersa, B. 2010: Udder health problems
and major of camel mastitis in Jijiga, Eastern Ethiopia: implication for
impacting food security. Tropical Animal Health and Production; 42:341
347.
Aboul, M.B . 1994: Reproductive performance of the one- humped camel
under traditional management in the United Arab Emirates. I Arid
environ, 26, 7-51
Abraham, G., Sintayehu, A., Libeau, G., Albina, E., Roger, F., Laekemariam, Y.,
Abyneh, D., Awoke, K.M. 2005: Antibody seroprevalence against peste
des petits ruminants (PPR) virus in camels, cattle, goats and sheep in
Ethiopia. Preventive Veterinary Medicine 70, 51-57.
Abu-Damir, H., Kenyon, S. J., Khalafalla, A. E., Idris, O. F. (1984): Brucella
antibodies in Sudanese camels, Tropical Animal Health and Production
16, 209-212.
Adan, M.S.: Indigenous camel management of the Gare tribe of Somali people
in northern Kenya. In: J.O. Evans, S.P. Simpkin and D.J. Atkins (Eds.):
Camel Keeping in Kenya. Range Management Handbook of Kenya,
Volume III, 8, Range Management Division, Ministry of Agriculture,
Livestock Development and Marketing, Republic of Kenya, 5.13-5.15
(1995). (Referenced livestock master plan study)
169
170
and obstrics. 5th ed. English Language book society, Bailliere Tindall,
Great Britain, pp. 483-487.
Ayele Solomon, Assegid Workalemahu, Jabbar M. A., Ahmed M.M. and
Belachew Hurissa, 2003: Livestock marketing in Ethiopia: A review of
structure, performance and development initiatives. Socio-economics
and Policy. Research Working Paper 52. ILRI (International Livestock
Research Institute), Nairobi, Kenya.
Baars, R.M.T., 1999: Costs and returns of camels, cattle and small ruminants in
pastoral herds in eastern, Ethiopia. Tropical Animal Health and
Production, 32 (2), 113-126
Bekele Megersa 2004: Sero-epidemiological study of brucellosis in camels
(Camelus dromedarius) in Borena lowland pastoral areas, southern
Ethiopia. Addis Ababa University, School of Veterinary Medicine. MSc
Thesis.
Bekele Megersa 2004: Sero-epidemiological study of brucellosis in camels
(Camelus dromedarius) in Borena lowland pastoral areas, southern
Ethiopia. Addis Ababa University, School of Veterinary Medicine. MSc
Thesis.
Bekele Megersa 2010. An epidemiological study of major camel diseases in the
Borana lowland, Southern Ethiopia. Drylands Coordination Groups (DCG)
Report No. 58
Bekele T. 2001. Studieson Cephalopia titillator, the cause of sengale in
camels (Camelus dromedarius) in semi-arid areas of Somali state,
Ethiopia. Tropical Animal Health and Production 33, 489-500.
Bekele T., Tezera, G., 1998: Preliminary observation on dromedary types and
major parasitic disease of camel in the eastern lowlands of Ethiopia. In:
Proceeding of the 6th Annual Conference. Ethiopian Society of Animal
Production, Ethiopia, 1415 May 1998, pp. 201207.
Bekele, S.T. 2008: Gross and Microscopic lesions of camels from Eastern
Ethiopia. Tropical Animal Health and Production, 40, 25-28.
Bekele, T. 1999: Studies on the respiratory disease, sonbobe in camels in the
eastern low lands of Ethiopia. Tropical Animal Health and Production, 31,
333-345.
Bekele, T. 2002: Epidemiological studies on gastrointestinal helminths of
dromedary (Camelus dromedarius) in semi-arid lands of eastern Ethiopia.
Veterinary Parasitology. 105: 139-152.
Bekele, T. and Molla, B. 2001: Mastitis in lactating camels(Camelus
dromedarius) in Afar Region, North-eastern Ethiopia, Berl Munch
Tierarztl Wochenschr 114, 16972.
Belachew Hurissa and Jemberu Eshetu, 2002: Challenges and opportunities of
livestock trade in Ethiopia. Paper presented at the 10th annual
conference of Ethiopian Society of Animal Production (ESAP), Addis
Ababa, Ethiopia, 222August 2002. ESAP, Addis Ababa, Ethiopia
171
Birhanu A., 1986: Survey of camel helminths in Hararghe region. DVM Thesis,
Faculty of Veterinary Medicine, Addis Ababa University, 42 pp.
Brown, A. 2004: A review of camel diseases in central Australia. Department of
Business, Industry and Resource Development. Arid Zone Research
Institute. Alice Springs, NT, Australia. 16 pages.
Bulliet, R. 1975: The Camel and the Wheel. Havard University Press, Cambridge
CARE-ETHIOPIA. 2009. Value chain analysis of milk and milk products in
borana pastoralist area . YONAD Business Promotion And Consultancy
PLC. Addis Ababa, Ethiopia
Carey R, ODonnell M, Ainsworth G, Garnett S, Haritos H and Williams G. 2008:
Review of legislation and regulations relating to feral camel
management, DKCRC Research Report 50. Desert Knowledge CRC, Alice
Springs.
Carter, G. R. 1984: Diagnostic Procedures in Veterinary Bacteriology and
Mycology, 4thed. Charles C. Thomas, Springfield, Illinois, U.S.A. pp. 3166.
Central Statistical Agency (CSA) 2009: Atlas of Ethiopian Rural Economy. Addis
Ababa Ethiopia.
Cervicek P. 1971: Rock paintings of laga oda (Ethiopia). Paideuma, Bd. 17:121136
Chartier, F., Chartier, C., Thovel, M. F. and Crespeau, F. 1991: A new case of
Mycobacterium bovis pulmonary tuberculosis in the dromedary
(Camelus dromedarius) in Mauritania. Revue D' Elevage et de Medicine
Veterinaire des Pays Tropicaux 44, 4347.
Chauhan, R.S., Gupta, S.C., Satiya, K.C., Kulshreshitha, R.C. and Kaushik. R.K.
1987: Bacterial flora of upper respiratory tract in apparently healthy
camels. Indian Journal of Animal Science 57, 424426.
Corne, J., Green, S., Sanderson, G., Caul, E., Johnston, S. 1999: A multiplex RTPCR for the detection of parainfluenza viruses 1-3 in clinical samples. J.
Virol. Methods. 82: 9-18.
Corsius J. 2011: Cultural Comparison about Camel Welfare between Animal
Scientists and Ethiopian Pastoralists. MSc Minor Thesis. Wageningen
University 9Accessed 9 JUNE 2012.http://www.ednahospital.org/
Dawood, H.A., 2008: Brucellosis in camels (Camelus dromedorius) in the South
province of Jordan. Am. J. Agric. Biol. Sci., 3: 623-626.
Dejene Milkessa 2010: Classical and molecular virological investigation of
emerging camel disease in Ethiopia. Addis Ababa University, School of
Veterinary Medicine. MSc Thesis.
Dereje, M., Udn, P. 2005: The browsing dromedary camel I. Behaviour, plant
preference and quality of forage selected. Anim. Feed Sci. Techol. 121,
297-308.
172
Dereje, M., Udn, P. 2005: The browsing dromedary camel II. Effect of protein
and energy supplementation on the milk yield. Anim. Feed Sci. Techol.
121, 309-317.
Dessalegn Belete 1984: Status report on small stock and camel research in
Southern Rangelands Project, ILCA, Addis Ababa, Ethiopia, 1 3.
Dioli, M. and Stimmelmary, R. 1992: Important camel diseases. In: The one
humped camel in Eastern Africa: a pictorial guide to disease, health care
and management. Livest. Sci. 36: 199-203.
Dirie, M. and Abdurahman, O. 2003: Observations on little known diseases of
camels (Camelus dromedarius) in the Horn of Africa. Rev. Sci. Technol.
Off. Int. Epiz. 22: 1043-1049.
Domenech, J., Guidot, T. G. & Richard, D. 1977: Pyogenic diseases of the
dromedaries in Ethiopia: symptoms and etiology. Revue D'Elevage et de
Medicine Veterinaire des Pays Tropicaux 30:3 251258.
Dungworth, D.L. 1993: The respiratory system. In: K.V.F. Jubb, P.C. Kennedy
and Palmer (eds), Pathology of Domestic Animals Vol. 2. Academic
Press, INC. Harcourt Brace Jovanovich, Publishers, San Diego, U.S.A. pp.
539699.
Elmi, A. 1989: Camel husbandry and management by Ceeldheer pastoralists in
Central Somalia. ODI Pastoral Devel. Netw. Pap. 27d, 36p. (referenced
livestock master plan study)
Epstein H. 1971: The origin of domestic animals of Africa. Vol. I. Africana
Publishing Cooperation, New York, USA.
FAO 1970 Vegetation and land use survey of Samburu District. UNDP/FAO
(Nairobi)
Farah, K.O. Nyariki, D.M. Ngugi, R.K. Noor I.M. and Guliye, A.Y. FARAH K.O. ET
AL.
Faye B., Saint-Martin G., Cherrier R., Ali Ruffa, 1992: The influence of high
dietary protein, energy and mineral intake on deficient young camel: I.
Changes in metabolic profiles and growth performance. Comp. Bioch.
Physiol., 102A, 409-416
Faye, B., 1997. Guide de lelevage du dromadaire (Sanofi, La Ballastiete,
France), 126
Fazil, M.A. 1977. The camel. Bulletin of Animal health and Production for
Africa. 25 (4): pp. 454462.
Fekadu, K., Girum, S. and Masse, M. 2003: Retrospective study of camel
respiratory disease complex in Afar region. Kombolcha Regional
Veterinary Laboratory. Kombolcha, Ethiopia. 23 Pages.
Fitsum Alemayehu 2011: Epidemiological and socio-economic investigation of
camel sudden death (CSD) and its relationship to peste des petits
ruminants (PPR) in Awash Fentale, Afar regional state, Ethiopia. Addis
Ababa University, School of veterinary medicine. MSc Thesis.
173
174
175
Kuchar, P., 1995b: Methods for evaluating range sites and range condition.
SERP Tech. Rep., Jijiga (Ethiopia), 83p. (Referenced in livestock
master plan study)
Kurtu, M. Y., 2004: An assessment of the productivity for meat and carcass
yield of camels (Camelus dromedaries) and the consumption of camel
meat in the eastern region of Ethiopia. Tropical Animal Health and
Production 36, 65-76.
Leese, A.S. 1927: A treatise on the one-humped camel in health and disease.
Stamford (Lincs.), Haynes and Son, 382 pp.
Lumadede, A. K, Owuor, G., Laqua, H., Gluecks, I. V. 2010. Save the Children
US. Pastoral Milk Production and Market Chain Analysis in the Somali
Region of Ethiopia
Mamo G, Kassaye A, Sanni M, Ameni, G., 2009: A cross sectional study of
camel tuberculosis in Ethiopia. Bulletin of Animal Health and Production
for Africa 57: 1. Medicine 55, 47 56.
Melesse B.G., 1995: Study on gastrointestinal parasites of the dromedaries in
Dire Dawa and eastern Oromiya. DVM Thesis, Faculty of Veterinary
Medicine, Addis Ababa University, Ethiopia, 46 pp.
Mesfin Weldemariam, 1970: An Atlas of Ethiopia. Rev. eds. Addis Ababa.
Moallin, A.S.M. & Zessin, K.H. 1988: Outbreak of camel contagious echthyma
in central Somalia. Tropical Animal Health and Production 20, 185186.
Mohammed Ali 2011: Pathological and bacteriological studies on Pulmonary
lesions of one humped camels (Camelus Dromedarius) slaughtered in
Oromiya zone of the Amhara national regional state, Ethiopia. Addis
Ababa University, School of veterinary medicine. DVM Thesis.
Moiser, D.A. 1994: Bacterial pneumonia Vet. Clin. North Am: food Aim
practice. 13(3): 483-491.
Mouchira, M. M 2009: Pathological Studies on Acariasis in Dromedary
(Camelus Dromedarius) and Llama (Lama glama) Camelidae. European
Journal of Scientific Research. 38 (2), 159-171.
Mukasa-Mugerwa, E., 1981: The camel (Camelus dromedarius): A bibliographical
review, (International Livestock Center for Africa, Addis Ababa, Ethiopia),
147
Munz, E., Schillinger, D., Reimann, M. & Mahnel, H. 1986: Electron
microscopical diagnosis of Ecthyma contagiosum in camels (Camelus
dromedarius). First report of the disease in Kenya. Journal of Veterinary
Medicine B. 33, 7377.
Musa, M. T. and Shigidi M. T. A., 2001: Brucellosis in camels in intensive animal
breeding areas of Sudan: Implications in abortions and early-life
infection. Revue Elev. Med. Vet. Pays. Trop., 54: 11-15.
Mussa, M and Greenhalgh P. 2007: Regoverning Markets: Small scale
producer in modern agri food markets. www. regoverningmarkets.org
National Geography. 2012. The salt and the earth.
176
Nell A.J., 2006: Quick scan of the livestock and meat sector in Ethiopia: Issues
and opportunities. Wageningen International. Wageningen University
and Research Centre. www.wi.wur.nl
Nesibu Awol, 2010: Pathological and bacteriological studies on pulmonary
lesions of one humped camels (Camelus dromedarius) slaughtered at
Addis Ababa abattoir enterprise, Akaki branch, Ethiopia. Addis Ababa
University, School of Veterinary Medicine. DVM Thesis.
Ngernawa J. J., Gathumbi P. K., Mutiga, E. R and Agumbu, G. J. 1993:
Pathogenesis of T. (brucei) evansi in small East African goats. Res. Vet.
Sci. 54: 283 289.
Njeuru, E. H. N., 1996: The application of indigenous knowledge in pastoral
production systems, (The African Pastoral Forum working paper series No.
6. University of Nairobi. Kenya), 17
Obied A. I. M., Bagadi H. O., Mukhtar N. M., 1996: Mastitis in Camelus
dromedarius and the somatic cell count of camels milk. Res. Vet. Sci.,
61: 55-58.
Odeh, F., Falah, K., Labib, A., Khaled, M., Yasin, A. and Nicholas, F. 1999: A
survey of camel (Camelus dromedarius) diseases in Jordan. J. Zoo. Wildl.
Med. 4: 335-338.
Omer Mohammed, Bekele Megersa, Rahmeto Abebe, Mesele Abera,
Alemayehu Regassa, Yunus Abdrehman and Solomon Mekur, 2011:
Seroprevalence of Brucellosis in Camels in and Around Dire Dawa City,
Eastern Ethiopia. Journal of Animal and Veterinary Advance 10 (9),
1177-1183
OWWDSE, 2010. Dawa Sub Basin Land Use Plan. Oromia Bureau of Land and
Environment Protection, Borena Zone
Patel, S.S.; Parikh, P.V.; Patil, D.B.; Kelawala, N.H.; Patil, V.N. and Jhala,S.K.
2007: Survey of surgical affections in camels 1996 2007. Camel
Conference-Book, International Camel Conference. Feb. 16 17,College
of Veterinary and Animal Science, Bikaner. P. 73.
Payne, W. J. A., 1990: An introduction to animal husbandry in the tropics. 4th ed.
(Longman Group Ltd, UK), 537-556
Pegram R. G., Hoogstral H. and Wassef H. Y., 1981: Ticks (Acari: Ixodidae) of
Ethiopia, I. Distribution, ecology and Host relationship of species
infecting livestock. Bulletin of Entomological Research, 71, 339-359.
PFE, IIRR and D.F. 2010: Pastoralism and Land: Land tenure, administration and
use in pastoral areas of Ethiopia
Pratt, D.J. 1966: Bush-control studies in the drier areas of Kenya. II. An
evaluation of the Holt IXa 'Bush Breaker' in Tarchonanthus/Acacia
thicket. J. Appl. Ecol. 3: 97-115. (referenced livestock master plan study)
Pratt, DJ and MD Gwynne, eds. 1977: Rangeland management and ecology in
East Africa.
177
Primary Industries standing committee model code of practice for the welfare
of animals. The camel (Camelus dromedarius). PISC report No. 86. CSIRO
Publishing, Australia
Purohit, N.R. and Chouhan, D.S. 1992: wound healing in camels. Proc.1st Int.
Camel Conf., Feb. 2 6, Dubai (UAE). 365 370.
Radostits, O. M., Gay, C.C., Hinchcliff, K. W., Constable, P. D. 2007: Veterinary
Medicine: A text Book of the diseases of cattle, sheep, pigs, Goats and
Horses, 10th ed. Saunders company, Philadelphia, U.S.A. pp. 471-541.
Radwan, A. I., Bekairi, S. I., and Prasad, P. V. S. 1992: Serological and
bacteriological study of brucellosis in camels in central Saudi Arabia.
Revue Scientifique et Technique de l ` Office International des Epizooties
11 (3), 837 844.
Richard, D. 1979: Study of the pathology of dromedary in Borena awraja
(Ethiopia). PhD thesis, Ecole Veterinaire, Alfort, IEMVT, France.
Roger, F., Gebre Yesus, M., Libeau, G., Diallo, A., Yigezu, L.M. And Yilma, T.
2001: Detection of antibodies of rinderpest and peste des petits
ruminants viruses (Paramyxoviridae, Morbillivirus) during a new
epizootic disease in Ethiopian camels (Camelus dromedarius), Revue
Md. Vt., 152, 265-268
Roger, F., Yigezu, M., Hurard, C., Libeau, G., Mebratu, G.Y., Diallo, A., Faye, B.,
2000: Investigations on a new pathological condition of camels in
Ethiopia. JCPR. 7 (2): 163165.
Rutagwende T., 1985: The control of important camel disease in the integrated
project of arid lands study area. Camel disease and productivity in the
arid lands of northern Kenya. Integrated Project in Arid Lands (IPAL).
Technical Report No. E-7, Germany, pp. 970.
Schmidt-Nielsen, K., 1997: Animal physiology: adaptation and environment,
5th ed. (Cambridge University Press, UK), 172-274
Schmitz H. 2005. Value chain analysis for policy-makers and practitioners. ILO
(International Labour Office), Geneva, Switzerland.
Schwartz H.Z. & Dioli M. 1992: The one-humped camel in Eastern Africa. A
pictorial guide to diseases, health care and management. Verlag Josef
Margaf, Schonwald Druck, Berlin, pp. 282.
Scoones, I., 1994: Living with uncertainty: new directions in pastoral development
in Africa, (Intermediate Technology Publication Ltd., UK), 210
Seifu E., 2007: Handling, preservation and utilization of camel milk and camel
milk products in Shinile and Jijiga Zones, eastern Ethiopia. Livestock
Research for Rural Development.19:6,
Simon M., 2010: "Kinematics of the southern Red Sea-Afar triple junction and
implications for plate dynamics". Geophysical Research Letters 37 (5):
L05301. doi:10.1029/2009GL041127.
Singh, H. 1966: Handbook of animal Husbandry for extension workers. New
Delhi, Ministry of food and agriculture, Director of Extension, p. 162
178
179
180