© The Author(s). 2017
Received: 6 October 2016
Accepted: 14 January 2017
Published: 20 February 2017
Animal breeds are the diverse outcome of the thousands-year-long process of livestock domestication. Many of these breeds are piebald, resulting from the artificial selection by pastoralists of animals bearing a genetic condition known as leucism, and selected for their productive, behavioural, or aesthetical traits. Piebald dromedary camels have not been studied or discussed before, and their same existence is often overlooked. Based on fieldwork in Western Sahara, direct observations across Northern and East Africa and the Middle East, and a literature review, we address the morphological and behavioural traits, geographical distribution, taxonomy, and material and cultural importance of piebald (painted) camels. They are a hundreds-year-old camel breed used for caravans, as mounts, and for aesthetical and cultural reasons across Sudan, Niger, Mali, Mauritania, Western Sahara, and Morocco. While they are increasingly bred out of a pastoral context for tourism and entertainment in the Canary Islands, mainland Europe, and the USA, in part of their original African range, piebald camels are under threat due to wars, droughts, and demise of pastoral livelihoods. More research is needed about these ‘beautiful and dignified’ animals.
KeywordsLivestock breeds Leucism Paint dromedary camels Pastoral nomads Sahara
A breed is a group of domesticates that has specific characteristics or traits artificially selected by man and transmitted through inheritance (Driscoll et al. 2009; Larson and Fuller 2014). Breeds are the diverse outcome of the thousands-year-long process of livestock domestication (Francis 2015). They have been selected in accordance to productive, cultural, and aesthetical traits and are often a key element of pastoral livelihoods and identities. Breed diversity is nowadays endangered by processes of livestock intensification and cultural homogenization (Faye et al. 2004), and as such, its study is a fundamental step for breeds’ conservation. Among the thousands of breeds from tens of domesticates existing in the world, several are piebald, i.e. spotted, painted, or patched of white and solid colour. Many of these piebald breeds are the result of a selective breeding for a genetic condition known as leucism.
Animals’ colouring is the result of either presence or absence of the pigment melanin in the skin, hair, and eyes. Among the known conditions affecting melanin production and animal colouring are albinism, melanism, and leucism; the latter resulting from defects in pigment cell differentiation and/or migration from the neural crest to the skin, hair, or feathers during development (Cieslak et al. 2011; Wilkins et al. 2014). In its most common form, leucism results in irregular patches on the body surface expressing as white on an animal that otherwise has normal colouring and patterning (Rook et al. 1998; Cieslak et al. 2011); when this happens, the animal is ‘pied’ or ‘piebald’ (also ‘paint’, ‘spotted’, or ‘speckled’).2 Some leucistic animals also exhibit coloration of the irises that matches the surrounding skin (blue eyes for pink skin, brown for dark).
Leucism and piebald colorations occur sporadically in the wild, as they usually reduce the individuals’ selective fitness providing less colour protection from predators (Woolf 1991). But recessive conditions in domesticates have been propagated voluntarily or not by humans since the very beginning of the domestication process, and changes in size and colour are among the first effects (Epstein 1955; Trut et al. 2009; Ludwig et al. 2009). Voluntary propagation includes the selective breeding of specific phenotypes for their religious, ritual, social, or subsistence/economic value. Involuntary propagation relates to the genetic and physiological links existing between tameness (a goal of early domesticators) and colour phenotypes (Wilkins et al. 2014; Cieslak et al. 2011; Price 2002) and to the effects of genetic drift in domesticates’ isolated populations (Zeder 2012). There is a general agreement that a wide variation of colour phenotypes were brought about by domestication, ‘but it is still largely unknown how color phenotypes were distributed in domesticated animals in earlier times, which roles they played for humans during these times and when they first occurred’ (Cieslak et al. 2011).
The piebald leucistic phenotype is known in a variety of domesticates, including Tobiano and Appaloosa horses (Brooks and Bailey 2005; Brooks et al. 2007), Belgian Blue and Shorthorn cattle breeds (Seitz et al. 1999), goats, and sheep, as well as dogs, cats, and pigs (Cooper et al. 2005; Giuffra et al. 1999). Several piebald animals have evolved into valued breeds, where Holstein cows and Dalmatian dogs are among the most notable examples.
Some of the genetic mutations related to the piebald character bear pleiotropic effects such as deafness, developmental disorders of the eyes and night blindness, and osteopetrosis (Stritzel et al. 2009; Bellone 2010; Wilkins et al. 2014). Because the development of the optical system is highly dependent on the presence of melanin, depigmentation has an effect on the development of the visual system (Grandin and Deesing 1998; Wilkins et al. 2014). Congenital stationary night blindness has been reported in a variety of spotted and piebald animals (e.g. Appaloosa horses; Sandmeyer et al. 2007). Animal breeders throughout the world have since early times recognized that a lack of body and eye pigmentation may be accompanied by neurological defects. A relationship between depigmentation and congenital deafness has been found, among other domesticates (Webb and Cullen 2010), in dogs (e.g. Dalmatian dogs with extensive white depigmented areas are most likely to be deaf; Strain 1996) and in llamas and alpacas (Camelids), where it is associated with pale blue eyes (Gauly et al. 2005).
A great deal of research has been conducted on the genetics, behavioural, and productive aspects of piebald breeds among several species (e.g. horses, dogs). In spite of this, the same existence of piebald camels has been largely overlooked, even in the scientific literature on camels (Wardeh 2004). Little and scattered information is available on piebald (painted) dromedary camels, and to the best of our knowledge, no single article has ever been written about them. The only author that has addressed their existence is Bulliet (1975), while too often it has not been properly acknowledged. For example, in the most recent and otherwise comprehensive book on animal domestication (Francis 2015), while discussing the correlation between coat colour and camel domestication, the author states that ‘In the United States, paint camels – white and brown, like pinto horses – have been produced, but paint camels are virtually absent in Arabia and North Africa.’ Though it is true that there are no painted camels in Arabia and East Africa, we contend that they indeed exist in North Africa since hundreds of years, and that the USA is just the latest country where they have been introduced after their diffusion westward from central-eastern Sahara, where they probably originated.
This paper departs from and contributes to the study of human-animal relationships and domestication from an historical and anthropological perspective (Bulliet 2005; Francis 2015; Hurn 2012). Most research on camels revolves around their potential as milk and meat producers and associated conditions (e.g. diseases) (Farah and Fischer 2004), whereas relatively less studies have been carried out on the productive and cultural links between pastoral populations and camels. In general, camel breeds are not as differentiated and classified as in other livestock species and their classifications are often derived from names of ethnic groups or geographical breeding regions rather than based on phenotypic characters (Dioli 2016). Therefore, camel breed study could help their conservation and support camel pastoralists (Kakar et al. 2011). Studies on the cultural relevance of piebald livestock (e.g. cattle) have already proven to be useful in describing complex human-animal relationships particularly in regard to livestock management (e.g. in genetic selection) and cultural identity (e.g. founding myths, cultural identity, and social values) (Coote 1994). In this paper, we address piebald camels’ physiological, genetic, and behavioural characteristics; their geographical distribution; taxonomy; and material and cultural roles among pastoral populations. Then, we discuss piebald camels’ origin and diffusion through Africa and out of Africa, we address trends in piebald camels’ husbandry, and we invite further research about and support to these ‘beautiful and dignified’ animals.
Location, duration, and time periods of fieldwork and direct observations
Type of study
1981 to 1991
1992 to 2013
Middle Shebelle (Jowhar)
Woqooyi Galbeed (Berbera)
1998 to 2001
Somali (Jijiga, Ogaden)
2003 to 2006
Gash-Barka (Barentu, Tesseney)
Northern Red Sea (Nakfa, Massawa)
Kingdom of Saudi Arabia
2006 to 2007
2007 to 2009
South Kurdufan (Nuba)
2008 to 2010
2009 to 2010
2010 to 2011
United Arab Emirates
Kingdom of Saudi Arabia
In-depth fieldwork was conducted in inland Western Sahara, northern Mauritania, and the part of Algeria to the south and south-east of the Hamada of Tindouf, which are the customary nomadic territories of Sahrawi pastoralists. Across this area, the climate is continental: summer daytime temperatures pass 50 °C, while winter night-time temperatures may drop to 0 °C. Rainfalls are torrential, unpredictable, and patchy, with an average annual rainfall of 30 to 50 mm and recurrent droughts. Generally occurring from the end of the summer through autumn, these rains are driven by the extreme northerly penetration of the African Monsoon from the south or are associated with the Atlantic Westerlies (Brooks et al. 2005). Biogeographically, we can distinguish two main areas: Zemmur to the north and Tiris to the south. The first runs east-west between northern Western Sahara and northern Mauritania: it is characterized by gravel plains with occasional surface of sandstone and granite in its eastern and central parts and by higher relief and hilly terrain in its western part. All Zemmur, and especially its central and western areas, is drained by inactive or occasionally active river channels that flow west into the Saguia el-Hamra, a large ephemeral river. After the rains, Zemmur displays a savannah-like environment dominated by Acacia-Panicum vegetation, while flowering prairies may appear on flat gravel areas. The southern sector, known as Tiris, is more arid and characterized by flat sand and gravel plains from which characteristic black granite hills arise in either clusters or in isolation. In Tiris, there are no dry riverbeds, and hence, vegetation is mostly herbaceous and adventitious and includes large areas covered by halophytic plants (Soler et al. 1999). For a background on the Sahrawi refugees and nomads and on their camel husbandry, see Volpato and Howard (2014) and Caro Baroja (1955).
The data analysed in this paper are drawn from three types of sources: (i) a review of scientific and grey literature about piebald camels and related topics, (ii) direct observations, and (iii) fieldwork carried out between 2008 and 2010 in the Sahrawi refugee camps of west Algeria and in Western Sahara.
Fieldwork included semi-structured interviews (n = 32) with Sahrawi camel owners (26 of them had piebald camels in their herds) about morphological, physiological, and behavioural characteristics of piebald camels and their uses and cultural values. Interviews were conducted in Hassaniya (the Arabic language with Berber substrate spoken by the Sahrawi), recorded and translated into Spanish by local research assistants. Interviews were recorded and transcribed with the help of the same research assistant to minimize translation errors and clarify information. Transcripts were then entered into NVivo qualitative data management software, and codes, concepts, and categories were generated during analysis. In every case, prior informed consent was obtained verbally before the interview was conducted, according to the ethical guidelines adopted by the American Anthropological Association (2009) and by the International Society of Ethnobiology (2006).
Besides fieldwork in Algeria and Western Sahara, direct observations on the presence (or absence) and distribution of piebald camels have been conducted by the authors in the Canary Islands (2006 to 2007), Sudan (2007 to 2009), Kenya (2012, 2015), Ethiopia (1998 to 2001), Eritrea (2003 to 2006), Somalia (2013), Yemen (2009 to 2010), Oman (2012), UAE (2010 to 2011), Kingdom of Saudi Arabia (2006), and Iran (2010) (Table 1). The areas where fieldwork and direct observations have been conducted are represented in Figure 1 with a focus on Africa, where piebald camels are found. While fieldwork included interviews about piebald camels, direct observations are reports from the authors on piebald camels’ presence in the areas where they have worked or conducted research and did not include interviews about piebald camels.
Results and discussion
Morphological, physiological, and behavioural characteristics
Physiological characteristics include various degrees of deafness and visual impairments, and the notion that piebald camels with blue eyes may have audio and visual impairments is well known to African camel pastoralists (Faye et al. 2002). These impairments are the reason pastoralists regard piebald camels as reckless, stubborn, disobedient, or particularly tame, even numb. Indeed, a relation between depygmentation and similar variations in behaviour is well established in the literature for other domesticates. Sometimes, there are different levels of deafness and auditive impairments in affected animals - and apparently different predominant behaviours - in relation to the level of depygmentation: for example, Holstein cows with complete depigmented white areas on their heads are among the calmest, while those that are mostly white on the body are nervous and intractable (Grandin and Deesing 1998).3 Similarly, Sahrawi herders describe piebald camels as having different levels of deafness, with an increased deafness according to the presence of blue eyes and white colouring of the head and toes. Conversely, ‘when a boldpie camel has normal hearing, its black ears and nails are the sign of it’ (Monteil 1952). Perhaps complete deafness is related to calm behaviour, whereas partial deafness or hearing distortions are related to increasing agitated and unpredictable behaviour. Complete deafness may also be at the base of Sahrawi and Tuareg herders’ description of piebald camels’ behaviour as ‘stubborn’, ‘non-obedient’, and ‘hard in understanding orders’, but also as being quiet and tame and ‘following the rest of the herd’ (Migeon 2006). According to Tuareg herders, ‘camels with blue eyes are real nuisances. They suffer from bad eyesight at night and consequently often get lost when camel caravans move in the dark’ (Curdy 2001). Some piebald bulls are attributed a ‘low ability in managing the herd’ due to these impairments.
But piebald camels are also appreciated for their alleged courage in crossing barren deserts (Cauvet 1925), as well as for their alleged resistance to hunger, thirst, heat, and fatigue during caravan journeys. While it is well known that camels can drink brackish and salty water, Sahrawi nomads mention that piebalds can tolerate even higher concentrations of salts in drinking water. The belief that piebald camels are more resistant to thirst and heat may be associated with the increased albedo of white and light-colour hair upon exposure to the sun.
Geography of piebald camels
There is little information about the presence of piebald camels in the eastern Sahara desert. Leese (1927), cited in Köhler-Rollefson (1991), reports the breeding of camels with mouse-coloured backs and necks and white bellies, faces, and legs in Kordufan and Darfur. Wilson (1978) states that ‘occasional parti-coloured camels also occur’ in southern Darfur.
Besides the Tuareg, other pastoral populations renown for breeding piebald camels are the Hassanyia-speaking nomads of Mauritania and Western Sahara (Correra 2006; Monteil 1952), also known as Moors or, in the northwestern part, as Sahrawi. Among them, piebald breeding is an old practice that has lasted to the present day, as is the case for the Reguibat, the Oulad Delim, and the Oulad Tidrarin tribes (Mercer 1976; Caro Baroja 1955; Boyer 1962), as well as among Moorish tribes of present-day northern and coastal Mauritania (Correra 2006). Relatively small numbers of piebald camels are also bred by neighbouring (non-Hassanyia-speaking) pastoralists such as the Chaamba of Central Algeria (Shinar (2004), in citing Cauneille (1968), states that they have ‘dappled (patched) grey, brown, and dark copper’ coloured camels) and the Marazig pastoralists of South Tunisia, reported to have camels with a white snout (Boris 1951).
In the literature about camels in the Canary Islands, the origin, significance, and distribution of piebald camels are never addressed, although their existence among the herds of the islands is usually recognized. Camels were first introduced to the Canary Islands beginning with the fifteenth century by the Castilian conquerors; during the course of the following centuries, camels adapted to the islands’ climate and were used by local peasants, particularly of Lanzarote and Fuerteventura, to power agricultural implements (e.g. ploughs, watermills), as a riding and pack animal, and for wheeled transport (Morera 1991; Schulz et al. 2010). Piebald camels were further imported to the Canary Islands from Western Sahara (possibly from individuals originally belonging to the Oulad Tidrarin, as this tribe was customarily living along the coast of Western Sahara adjacent to the Canary Islands, with which it had historical commercial contacts). Indeed, a recent study has shown a clear genetic proximity between camel populations from the Canary Islands and from western Africa (Schulz et al. 2010), and Canary Islands’ piebald camels are reported as closely related to the piebald ‘Western Sahara’ breed (Dioli 2013), from which they likely originated. But when this happened is uncertain.
Genetics of piebald camels
The piebald character is usually transmitted by one or more recessive genes that is (are) also responsible for blue eyes, congenital deafness, and impaired vision. Involvement of more genes and mutations make the genetics of leucistic animals complex (Householder 2003), and ‘the genetic pathways influencing coat coloration are still only poorly described’ (Cieslak et al. 2011). Unsurprisingly, given the lack of attention to leucism in camels in the scientific literature, no investigation has up to now been conducted on the genetics of piebald camels. From the information we collected, only a tentative hypothesis can be put forward, and in order to have a deeper understanding of piebald camels’ genetics, a ‘herd analysis exercise’ (Krätli 2008) among herds including piebald camels would be helpful.
In general terms, Sahrawi herders state that a piebald bull introduced into a non-piebald herd results in a 30% to 50% of piebald calves (males in most of the cases), that a piebald calf can be produced by two solid-coloured parents if there was a piebald in the family, and that conversely two piebald parents can produce solid offspring. According to the Sahrawi, piebald coloration and associated characteristics are transmitted to calves by blue-eyed piebald fathers. If the bull is not piebald, piebald calves are born in a relation of one third or one quarter to the number of piebald mothers. Hence, piebald condition in camels seems to be sex related, with males displaying the colouring pattern more often than females. Indeed, most of the piebald camels we saw during fieldwork in Western Sahara were males. Further insights can be obtained by comparing piebald camels’ genetics to that of other mammals, as it appears that there is a common genetic mechanism that determines coat colour (Wilkins et al. 2014). In Appaloosa horses, for example, the piebald expression is controlled by a single gene, which is apparently dominant, and displays the piebald pattern when two series of modifying genes are expressed: one series for the control of the expression of white (vis-à-vis the normal coat colour) and another series for the expression of spots (Householder 2003). Apparently, the expression of the white modifier and the spot genes are sex influenced, with heterozygote individuals expressing the characteristic when males, and not when females (Householder 2003), like in camels. In Dalmatian dogs, the piebald character is given by two recessive genes, with individuals displaying the phenotype when homozygous; the expression of the spotted colouring is farther related to the expression of genes for congenital deafness and blue eyes (Strain 1996), as seen in camels. The genetics of piebald camels may indeed involve not just one but more genes like in Appaloosa horses and Dalmatian dogs. Differently, in Holstein cattle, the piebald effect seems to be due to inheritance of a single piebald spotting gene, with no sex differentiation (Pape 1990), unlike in camels.
Throughout their range and among all the populations who breed them, piebald camels are known by names that recall their piebald coat or their blue eyes, less often their peculiar behavioural characteristics. Most names have an Arabic root.
Among Arabic-speaking populations (e.g. the Hassanyia-speaking Sahrawi and Moors and the Arabic-speaking Sudanese pastoralists), piebald camels are known as azraq (male), zarqa (female), or zurq (plural) (Taine-Cheikh 1989; Caro Baroja 1955). In classical and contemporary Arabic, zurq means ‘blue’, but also ‘blue-eyed’, ‘blue, minnow, or glittering eyes’, and ‘glaucoma’ (Fischer 1965). Though not in reference to piebald camels, the term has among some Maghreb populations a positive aesthetic connotation, with a female or woman called zarqa in reference to her sensual beauty (Roth 1985). In Hassanyia, the verbs stazrag and zrāg mean ‘being towards piebald coloration (of camels)’ and ‘becoming piebald’, respectively (Taine-Cheikh 2002), and azraygat their diminutive (Voisset 1989). The term zurq applied to coat colour is used also for a grey coat, especially in reference to horses and cattle (Roth 1985) but also in reference to camels, e.g. in Arabia (Abbas et al. 2000); nevertheless, to the Zaer of North Morocco, a zurq cattle is a cattle with white patches all over its body (Loubignac 1952). Interestingly, in colloquial Arabic there exists a derived term mizra:qan, used to indicate a camel delayed behind the rest of the caravan because it moves slowly (Allam 2000), which may be in relation with the tendency of some piebald camels to stray away. In Morocco and Western Sahara, the term zeroual is also used to indicate piebald camels, as well as people and camels with blue eyes.
There is a strong consistency in the terms used for piebald camels across time and space: they all originate from the Arabic zurq. The Tuareg use the zurq-derivated term azarghaf, not of Berber Tamasheq (Tuareg’s language) origin. This fact takes more significance when we consider that Tamasheq has a low proportion of Arabic loanwords, and usually few of these with regard to phytonymic and zoonymic terms: items lended/adopted from one population to the other are more likely to have the same etimology, and piebald camels and their zoonym may have been historically adopted by Tamasheq-speaking Tuareg from Arabic populations.
Zurq is also the etymological origin of some Spanish words, notably ‘zarco, −ca’ which means light blue, azure, and ‘ojizarco, −ca’ which means ‘blue-eyed’. Among Spanish-speaking piebald camels’ breeders of the Canary Islands, names for piebald camels also refer to their coat colour or to their impairments and associated behaviour. Piebalds are known as manchado or pintado (spotted or painted) when with white patches on the body or some of its parts and as capiloto when displaying a white head and a prevalently normal-coloured body (cfr. the Spanish capirote, i.e. cattle with the head and the body of different colours; Morera 1991). Among present-day Sahrawi of Western Sahara (a former Spanish colony), besides as zurq, piebald camels are also referred to as colorín (coloured) or camellos zonzos or tontos (silly, fool camels).
Material and cultural importance
Piebald camels have different material and cultural roles among the distinct populations engaged in their breeding. These roles encompass subsistence material uses (e.g. for milk and meat production, transport, and caravans), a cultural importance in terms of aesthetics, cultural identity, and tribal/group identification, as well as the recent use of income generation out of a pastoral context.
In the Saharan areas where they are bred, piebald camels have been often used by different populations as pack camels for caravans, for transport (e.g. moving to new grazing areas), and as mounts because they are prevalently male and/or because of their resistance to thirst and heat and/or because their physiological impairments make them more tame. Among the nomads of Western Sahara and Mauritania, they were used in pre-colonial times as mounts by blacksmiths and griots as well as in caravans (Monteil 1952). They are used in caravans, particularly in areas with sandy soils (Migeon 2006), such as in Niger (Chaibou 2005; CIRAD 2001), where this breed is known ‘for its resistance and courage with which it crosses the desert from the Aïr to Bilma’ (Cauvet 1925). Indeed, they are used for the annual tarlamt, which are the salt caravans moving across the Ténéré desert from Agadez, Zinder, or Tahoua to the salt deposits of Fachi and Bilma in Niger (Cianchini 1999). In Morocco, they are used as mounts and to transport merchandise to towns (Driot 2009). In Nigeria, they are regarded as ‘very faithful beasts of burden used essentially for personal transportation, to carry loads, draw water, and pull ploughs’.10
In the Canary Islands, piebald camels are bred mainly to transport tourists (particularly in the island of Lanzarote), who seem to be particularly attracted to their variegated colouring and blue eyes (Dioli 2013). Nowadays, there are about 1,000 camels in the Canary Islands (Schulz et al. 2010), and they are almost completely used in the touristic industry. Many of them are piebalds. From the Canary Islands, piebald camels have been exported during the last decades to European and American countries (Castillo and Lugo 2003). In the USA, piebald camels are much appreciated aesthetically and valued two to three times the price of a solid-coloured camel (Berry 2006).11 The value of a piebald calf ranges between $3,000 and $6,000.12 , 13 Two farms in Tennessee hire their piebald bulls for breeding, while one farm in North Carolina, specialized in breeding ‘of rare and exotic animals’, sells its paint camels to private people or provide them for hire for tourist ‘safari’ (in ranches), commercials, theatre performances, and plays.14 Another ranch in Texas owns some fine piebalds (see pictures in the website)15; according to the statement in their website, they are breeding ‘for bigger and better spotted camels’.
Among Sahrawi and Tuareg breeders, piebalds are appreciated for their beauty in terms of variable patterns of coloration and blue eyes. They have become a marker of cultural identity and have been incorporated in poems, literature, folk knowledge, and foundation myths. They are considered a locus of visual stimulation and a source of positive emotions. Their high variability in coat colouring patterns have become an ownership mark with similar functions to those of customary livestock brands.
Sid Ahmed Bo Gambar, one holy ancestor of the Oulad Tidrarin, was one day praying on the beach, when suddenly an azrag [piebald] camel came out from the sea. Sid Ahmed took the camel, which was a stud, and from this camel the many azrag camels the Tidrarin owns descend
This myth attributes the origin of piebald camels to a miracle done by Sid Ahmed and explains the attachment and sense of identity that the members of the tribe have for these camels. In fact, nowadays, piebald camels are still a marker of cultural identity for the Sahrawi nomads (including the members of the former tribes of Western Sahara), who breed them particularly for their perceived beauty and the prestige derived from it.
The fact that leucism considerably varies the ratio of white to coloured hair between generations as well as between offspring from the same parents gives each individual a specific and recognizable pattern, which has often attracted pastoral populations (Rook et al. 1998). Sahrawi’s and Tuareg’s appreciation of piebald camels recalls the anthropology of aesthetics as discussed, for example, in the case of cattle among Nilotic populations (Coote 1994). Among the Mandari, a piebald ox is highly appreciated and, when a piebald is born, its owner is delighted and the beast is set aside for show (Buxton 1973). The high aesthetic value that the Mandari place on cattle patterning is explained by Buxton (1973) by the fact that, ‘they stand out strikingly in a landscape devoid of strong color’, where the individual beast provides the locus for stimulating visual experience (Coote 1994). Indeed, aesthetic explanations related to their striking and coloured appearance on an otherwise pale landscape are as appealing to camel-breeding nomads as they are for the cattle-breeding Mandari. Camels at the horizon are a common visual locus when travelling in Western Sahara. As piebald camels strike on the yellow horizon with a colour pattern variety, and as these coloured shapes vary from animal to animal, it is no wonder that a piebald camel represents a particularly appreciated visual stimulation.
Among the Tuareg, piebald camels are associated with beauty. To communicate their sense of beauty, Tuareg poets link man, camels, and pastoral resources. Piebald camels find a place in these poems. In one of them,17 the beauty of a girl is put in analogy with that of a piebald camel (Ghabdouane and Prasse 1990). Similarly, in a recent novel describing the commitment between a man and his piebald camel written by Al-Koni (2008), himself a Tuareg raised in the desert of Libya, a Tuareg nomad is constantly lauding his piebald mahri for the unique colouring of his pelt, in spite of its undisciplined and reckless behaviour. During a passage of the novel, a local sheikh entraps the beautiful piebald to get it to impregnate the sheikh’s she-camels and obtain calves from the piebald strain. In the sheikh’s words, it was ‘a piebald mahri as graceful as a gazelle. This line became extinct throughout the desert a hundred years ago’ (Al-Koni 2008). The blue eyes and coat colour and pattern of piebald camels have historically been at the centre of different emotional and rational attachments by their herders and are also much appreciated among tourists travelling to the Canary Islands and south of France, children visiting zoological parks (e.g. in Tunisia), and owners of rare and exotic animals in the USA.
Are piebald camels a breed?
Wardeh (2004), in his classification of dromedary camels, does not refer to the existence of piebald breeds or individuals, whereas several other authors have described piebald camels as a camel breed/race (Pacholek et al. 2000b; Monteil 1952; Antoine-Moussiaux et al. 2007). From the information we collected, it seems that the piebald character may theoretically be present or introduced into different existing camel breeds, thus being a characteristic linked to different breeds (e.g. a piebald mahri) but it can also prevail over the traits of the existing non-piebald breed leading to the development of a new piebald breed. We can envision two ways through which a piebald camel breed originates: (1) A piebald camel (of a non-piebald existing breed) is born within a herd, and local herders, once it is sexually mature, favour its reproduction; (2) A piebald camel, preferably a bull, is introduced (e.g. through raid or purchase) into a herd with no piebald camels and selected for reproduction. By further selecting at the same time for the piebald character and for the characters of the original breed, the outcome in the long run will be piebald camels of the original non-piebald breed. However, protracted selection for the piebald character (rather than for the traits of the original breed) may create not a breed variant but new piebald breeds. In both cases, favouring the reproduction of piebald traits increases the pull of leucistic alleles in the herd (and then in local herds), so that in the long run, piebald camels are born with higher frequency. However, we have seen that piebald individuals are commonly a minority within herds due to the constraints of inbreeding and to the recessive character of leucism and these facts weight the balance toward considering ‘piebaldness’ a breed variant, maybe in the process of becoming a breed.
Origin and diffusion of piebald camels
When and where domestication took place is still controversial for many species, and Cieslak et al. (2011) suggest that ‘at least in some cases, coat and skin color can be a valuable marker for resolving these discussions.’ Although the question of camel domestication has been complicated and frustrating for many scholars, there is some agreement that the camel, after having been hunted between 6000 and 3500 BC, has become the focus of direct domestication in the third millennium BC probably in south Arabia (Clutton-Brock 1988; Bulliet 1975, Zeder 2012). Sherratt (1983) suggests that camel domestication took place in two developing zones of long-distance trade (Bactrian camel toward the east, dromedary camel towards the south-west) in relation with the growing urban area of Mesopotamia. The camel as a pack and military animal was at its greatest expansion during the Nabatean times (second century BC - first century AD), during which period camels would have been taken up by populations in the eastern Egyptian desert (e.g. the Beja).
Camels had been replacing cattle and horses throughout the southern edge of the Sahara from approximately the third century BC, and a variety of populations of camel nomads have subsequently developed from Sudan to Mauritania and Western Sahara, through Niger, Mali, and Algeria. There is some agreement among scholars that camels spread westward through Africa first from a south-Saharan route going from Sudan to Mauritania about 2,200 years ago and shortly later through a north-Saharan route, reaching western Sahara from both routes about 2,000 years ago (Blanc and Ennesser 1989; Wilson 1984; Bulliet 1975). The diffusion of camel husbandry and nomadism facilitated a growth of a trans-Saharan caravan trade in the north-south and east-west directions. Indeed, the trading route going from Sudan and the Nubian desert to Timbuktu in Mali, and passing through Darfur, Kano, lake Chad, and Gao, was active and established already in 1400 (Wolf 1982).
The camel nomads of southern Sahara developed their own distinct forms of livelihoods and culture (e.g. in uses of camels and camel products, saddle technologies, taste, and aesthetic preferences), which included a preference for piebald camels. This preference, combined with the trans-Saharan exchange networks, facilitated the diffusion of piebald camels. Indeed, ancient Egypt and Sudanese nomadic populations were known for appreciating and venerating piebald cattle (d’Alverny 1950), and a breeding preference for piebald livestock (e.g. cattle, sheep) was already established in the region before the camel’s introduction. This preference may have combined with a genetic drift occurring in the relatively low number of camels supported by the Saharan environment and taking part in this westward dissemination. This genetic drift may have caused the appearance of otherwise relatively rare conditions such as leucism and the associated piebald traits. This may at the same time explain the lack of piebald camels in Arabia and Somalia, where camels were present in huge numbers since the dawn of camel domestication and where leucism would have been quickly damped out by the much broader gene pool. All this suggests that the pioneer piebald camel breeders were relatively few, their livestock herds small in size, and their ability to control breeding well developed (Bulliet, pers. comm.).
From western Sudan, piebald camels would have spread (through raids, exchanges, and purchases) westward and their breeding being taken up by the southern Tuareg first and by Moorish populations of Western Sahara and Mauritania then (Figure 8). For example, according to Mahaman (1979), ‘[azarghaf camels] can be held by other ethnic groups who purchase them from the Tuaregs to use them essentially as pack animals.’ This supports the hypothesis that piebald camels of Western Sahara find their origin from purchases at the markets of Niger, as expressed by older living members of the Reguibat tribe: the first piebald camel - they say - was a bull brought from the east about four centuries ago (between the sixteenth and the seventeenth centuries).
The paths of camel diffusion support the idea that similar paths have been used by piebald camels in their diffusion and the contemporary distribution of piebald camels supports the idea that they spread through a south-Saharan route. Through this route, piebald camels were adopted and bred by populations who had already shown an appreciation for other piebald livestock. During the following centuries, piebald camels spread through the Sahara from east to west of Africa, and further into the Canary Islands, Europe, and the USA. Overall, the history of piebald camels have much in common with the history of other piebald breeds around the world, as, for example, the one of splashed white Icelandic horses.18 Splashed white blue-eyed horses of Iceland are the outcome of a genetic drift that isolated the population coupled with a recent upsurge in an aesthetical preference for these traits among Icelandic horse breeders.
Trends in piebald camels today
Based on the total number of camels known to occur in piebald breeding areas, on piebald genetics, and on direct observations, we roughly estimate that there may be less than 5,000 piebald camels in the world. Most are in Niger and Western Sahara, bred by the Tuareg and the Sahrawi, respectively. In different areas, piebald camels are subjected to distinct trends affecting their numbers and material and cultural importance.
At least three different major contemporary trends can be identified as involving piebald camels: (1) their decline due to the abandonment of nomadic livelihoods (due to droughts, wars, destocking, etc.) and due to camel commodification and market pressures against piebald camels; (2) their disengagement from a pastoral economy and their use as source of income in the touristic and entertainment industries due to their aesthetical qualities; and (3) a resurgence of piebald camel breeding as a marker of political and cultural identities.
The first trend seems to be taking place in Sudan due to expansion of crop farms, droughts, and wars (Musa et al. 2006), as well as in Niger due to market pressures. In both areas, the demise of caravans in favour of motorized transport during the last century has surely contributed to a progressive reduction of piebald camel husbandry, the more so considering their widespread use in caravans. In Niger, there seems to be an ongoing process of further disengagement by many Tuareg herders. According to Pacholek et al. (2000a), piebald camels in the south of the Aïr are threatened by ‘absorption’ by the other two non-piebald local camel breeds, the azawak and the manga. This is attributed to the fact that ‘the monetarization of pastoral societies pushes herders to turn to the breeding of types with the highest market value’, and as piebald camels are less valued (e.g. for milk and meat production) on local markets, herders introduce non-piebald bulls into their herds (Pacholek et al. 2000b).
The second trend is evident in the Canary Islands and the USA, where piebald camels are actively bred and used in the touristic and recreational industries. Ranches in the USA have started raising piebald camels during the last two decades: they are appreciated aesthetically; they have higher monetary value than solid-coloured camels and are actively sold or hired to a variety of actors (Berry 2006), thus further spreading in new areas of the world, albeit out of a pastoral context.
Although camel breeds have been historically important in the ability of pastoral populations to adapt and better exploit the desert environment, with increasing commoditization of camels and camel products, there is the risk that some locally adapted camel breeds may be diminishing in population and slowly disappearing (Blanc and Ennesser 1989). With the possibility that negative trends may prevail in different areas of Africa, it is urgent to study piebald camels and cultures around them. In reference to Nigerien piebald camels, studies report that it is undergoing a ‘progressive disappearing of a type [of camel] with marked characteristics…and maybe unique…This danger deserves to be taken in consideration in regard to the safeguard of…biodiversity’ (Pacholek et al. 2000b), as well as cultural diversity.
This study has addressed the history, geography, and anthropology of piebald camels. Based on fieldwork among the Sahrawi of Western Sahara, direct observations across north and east Africa and the Middle East, and a literature review, the case illustrates how piebald camels are an integral part of the story of the camel and of camel pastoralists in Africa and how piebald breeds are an interesting case to understand the dynamic relations of pastoralists with their livestock. Piebald camels probably originated in the eastern Sahara hundreds of years ago from a mutation that was picked up and selected for by local pastoralists who already had a preference for piebald livestock. In the ensuing centuries, piebald camels spread westward throughout Africa while being adopted by distinct pastoral tribes and groups across present-day Sudan, Niger, Mali, Mauritania, Western Sahara, and Morocco. They were bred for their alleged docility, for resistance to heat and thirst, and for their aesthetical value and were used in caravans and as mounts, as well as for subsistence purposes (e.g. milk and meat production) and for cultural reasons (e.g. as marker of cultural identity). During the last decades, piebald camels have been exported to the Canary Islands, Europe, and the USA, where they are used out of a pastoral context in the touristic and entertainment industries due to their perceived beauty and tameness.
The findings of this study are significant for understanding trends related to breeds and breeders in contexts of historical and contemporary change in pastoral systems. The findings also contribute to providing insights into the more general process of human selection for piebald colorations in domestic animals. This process can have different drivers and motives in different socio-ecological contexts and time. Piebald camels are under threat due to wars and droughts that kill herds and undermine pastoral livelihoods, e.g. in Darfur. They are threatened by increasing commodification of camels and camel products and consequent herd homogenization towards breeds with high marketing value, e.g. in Niger. Piebald camels and their husbandry have seen a resurgence during the last two decades as a symbol of political and cultural identity, in Western Sahara. Further studies are needed to fully elucidate the biology and history of piebald camels and their roles and dynamics in the present and in historical time. Fieldwork in other geographical areas (other than Western Sahara) where piebald camels are bred would be of great help in this sense. Also, a genetic study may help to identify different strains and to reconstruct piebald camels’ temporal and geographical evolution and diffusion. A research into old written sources, mainly of Arabic origin, could help clarify the timing when piebald camels came to the Saharan Africa. Further studies would also be interesting to understand the place of piebald camels as an aesthetic locus among desert pastoralists. Such studies could make an interesting contribution to the field of anthropology of aesthetics.
We have pointed out that, in distinct breeding areas, piebald camels are subjected to negative trends, which increase the possibility of losing important genetic traits as well as the associated biocultural diversity (e.g. genetic, knowledge, and management). If these negative trends prevail, we risk losing the results of centuries-old engagement of humans in piebalds’ breeding. The full story of piebald camels may be lost before having the chance to be told.
A mahri or mehari is a Sahelian riding camel
It is important to clarify the distinction between piebald animals whose white areas are depigmented (e.g., Dalmatian dogs, Overo and Tobiano horses), and those that have a white coat color but are fully pigmented (e.g., Arab horse, Brahman cattle) (Granding and Deesing 1998); only the former are leucistic animals.
Holstein cows with blue eyes are nowadays selected against and excluded from inclusion in the European Union register of accepted breeds.
Inbreeding this kind of animals might cause neurological abnormalities, as it has been shown for dogs and cats (Grandin and Deesing 1998).
Ezzara, tu es plus belle que les jeunes chamelles au milieu desquelles se dresse un étalon brun Celui aux taches noires sur la croupe et la tête, ce chameau pie aux (aisselles) blanches…’
We are very thankful to many Sahrawi refugees and nomads for their patience, kindness, and hospitality during the interviews. We also thank the Italian NGO Africa’70 and the Sahrawi Veterinary Services of the SADR (Sahrawi Arab Democratic Republic) for logistical support and cooperation. We thank Alessandro Broglia, Davide Rossi, Saleh Mohamed Saleh, and Sidahmed Fadel for helping during fieldwork and Anna Littlejohn for editing the manuscript. Our thanks go also to Prof. Richard Bulliet for his insights on piebald camels and his comments on the manuscript.
Funds were granted to GV by the Ceres Research School of the Wageningen University, The Netherlands, as part of his PhD research on recovery and adaptation of subsistence practices and ethnobiological knowledge among the Sahrawi refugees. ADN was supported by the BBSRC DTA grant (1094618 and BBS/E/I/00001642) and by the BBSRC Institute Strategic Programme Grant on Livestock Viral Diseases to The Pirbright Institute, UK.
GV and partly ADN carried out the fieldwork in Western Sahara. Observational studies in Arabia, Sudan, and the Horn of Africa were conducted by MD, while GV and ADN compiled direct observations in Kenya. GV, MD, and ADN composed the literature review and drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
In every case, prior informed consent was obtained verbally before the interview was conducted, according to the ethical guidelines adopted by the American Anthropological Association (1998) and by the International Society of Ethnobiology (2006).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
- AA. 2000. Proceedings of the international workshop on the camel calf. Revue d Elevage et de Medecine Veterinaire des Pays Tropicaux 53(2): 1–138.Google Scholar
- AAA. 2009. Code of Ethics of the American Anthropological Association. http://s3.amazonaws.com/rdcms-aaa/files/production/public/FileDownloads/pdfs/issues/policy-advocacy/upload/AAA-Ethics-Code-2009.pdf. Accessed 18 Jan 2017.
- Abbas, B., A.A. Al Qarawi, and A. Al Hawas. 2000. Survey on camel husbandry in Qassim region, Saudi Arabia: Herding strategies, productivity and mortality. Revue d Elevage et de Medecine Veterinaire des Pays Tropicaux 53(3): 293–298.Google Scholar
- Al-Koni, I. 2008. Gold dust. Translated by E. Colla. London: Arabia Books.Google Scholar
- Allam, J. 2000. A sociolinguistic study on the use of color terminology in Egyptian colloquial and classical Arabic. In Diversity in Language. Contrastive Studies in English and Arabic Theoretical and Applied Linguistics, ed. Z. Ibrahim, N. Kassabgy, and S. Aydelott, 77–92. Cairo and New York: The American University in Cairo Press.Google Scholar
- Antoine-Moussiaux, N., B. Faye, and G. Vias. 2006. Connaissances ethnovétérinaires des pathologies camélines dominantes chez les Touaregs de la région d’Agadez (Niger). http://camelides.cirad.fr/fr/science/pathotouareg1.html:1–21.
- Antoine-Moussiaux, N., B. Faye, and G. Vias. 2007. Tuareg ethnoveterinary treatments of camel diseases in Agadez area (Niger). Tropical Animal Health and Production 39: 83–89.View ArticleGoogle Scholar
- Bellone, R.R. 2010. Pleiotropic effects of pigmentation genes in horses. Animal Genetics 41: 100–110.View ArticleGoogle Scholar
- Bernus, E. 1969. Maladies humaines et animales chez les Touaregs sahéliens. Journal de la Société des Africanistes 39(1): 111–138.View ArticleGoogle Scholar
- Berry, R. 2006. Spotted camels. http://camelphotos.com/spotted.html. Accessed 27 Jan 2017.
- Blanc, C.P., and Y. Ennesser. 1989. Approche zoogéograpique de la différenciation infraspécifique chez le dromadaire Camelus dromedarius Linné, 1766 (Mammalia: Camelidae). Revue d Elevage et de Medecine Veterinaire des Pays Tropicaux 42(4): 573–587.Google Scholar
- Boris, G. 1951. Le chameau chez les Marazig. Notes lexicographiques, 57–72. I.B.L.A.Google Scholar
- Boyer, J.R. 1962. Contribution à l’étude de l’élevage camelin au Sahara Occidental. Le Regueibat et son chameau. Diplome d’Etat, Faculté de Médecine de Paris, Ecole Nationale Veterinaire D’Alfort.Google Scholar
- Brooks, S.A., and E. Bailey. 2005. Exon skipping in the KIT gene causes a Sabino spotting pattern in horses. Mammalian Genome 16: 893–902.View ArticleGoogle Scholar
- Brooks, N., I. Chiapello, S. Di Lernia, N. Drake, M. Legrand, C. Moulin, and J. Prospero. 2005. The climate-environment-society nexus in the Sahara from prehistoric times to the present day. The Journal of North African Studies 10(3–4): 253–292.View ArticleGoogle Scholar
- Brooks, S.A., T.L. Lear, D.L. Adelson, and E. Bailey. 2007. A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses. Cytogenetic and Genome Research 119: 225–230.View ArticleGoogle Scholar
- Bulliet, R. 1975. The camel and the wheel. Cambridge: Harvard University Press.Google Scholar
- Bulliet, R. 2005. Hunters, herders, and hamburgers. The past and future of human-animal relationships. New York: Columbia University Press.Google Scholar
- Buxton, J. 1973. Religion and healing in Mandari. Oxford: Clarendon.Google Scholar
- Caro Baroja, J. 1955. Estudios Saharianos. Madrid: Consejo Superior de Investigaciones Cientificas.Google Scholar
- Castillo, I. del, and B. de Lugo. 2003. De la llegada de los camellos a las Canarias. http://www.camellosafari.com/camellos/camellos.html. Accessed 27 Jan 2017.
- Cauneille, A. 1968. Les Chaanba (leur nomadisme), évolution de la tribu durant l’administration française. Paris: Éditions du Centre national de la recherche scientifique.Google Scholar
- Cauvet, G. 1925. Le Chameau (anatomie, physiologie, races extérieur, alimentation, maladies, raIe économique). Paris: Librairie J. B. Bailliere et Fils.Google Scholar
- Chaibou, M. 2005. Productivité Zootechnique du Desert: Le Cas du Bassin Laitier d’Agadez au Niger. Docteur es Sciences, Biologie des Systèmes intégrés, Agronomie, Environnement, Université de Montpellier II.Google Scholar
- Chaibou, M., and B. Faye. 2003. Production latiére des chamelles Abzin élevées par les Touaregs nomades du Niger. Niamey: Lait du chamelle pour l’Afrique. Atelier sur la filiére caméline en Afrique.Google Scholar
- Cianchini, D. 1999. L’ultima carovana del sale.. Africa.Google Scholar
- Cieslak, M., M. Reissmann, M. Hofreiter, and A. Ludwig. 2011. The colours of domestication. Biological Reviews 86(4): 885–899.View ArticleGoogle Scholar
- CIRAD. 2001. La répartition géographique des races des grands camélidés dans le monde. Centre de coopération internationale en recherche agronomique pour le développement, accessed 17 Oct.Google Scholar
- Clutton-Brock, J. 1988. The walking larder: Patterns of domestication, pastoralism, and predation. Google Scholar
- Cooper, M.P., N. Fretwell, S.J. Bailey, and L.A. Lyons. 2005. White spotting in the domestic cat (Felis catus) maps neat KIT on feline chromosome B1. Animal Genetics 37: 163–165.View ArticleGoogle Scholar
- Coote, J. 1994. ‘Marvels of everyday vision’: The anthropology of aesthetics and the cattle-keeping Nilotes. In Anthropology, Art, and Aesthetics, ed. J. Coote and A. Shelton, 245–273. Oxford: Oxford University Press.Google Scholar
- Correra, A. 2006. Dynamique de l’utilisation des ressources fourrageres par les dromadaires des pasteurs nomades du Parc National du Banc d’Arguin (Mauritanie). PhD, Ecologie et gestion de la biodiversité. Museum National d’Histoire Naturelle de Paris.Google Scholar
- Curdy, A. 2001. Never trust a camel with blue eyes. Field Exchange 13.Google Scholar
- d’Alverny, F. 1950. Vestiges d’art rupestre au Tibesti oriental. Journal de la Société des Africanistes 20(2): 239–272.View ArticleGoogle Scholar
- Dioli, M. 2013. Pictorial guide to traditional management, husbandry and diseases of the one-humped camel.. Photographic CD-ROM.Google Scholar
- Dioli, M. 2016. Towards a rational camel breed judging: A proposed standard of a camel (Camelus dromedarius) milk breed. Journal of Camel Practice and Research 23(1): 1–12.Google Scholar
- Driot, C. 2009. Etude epidemiologique et histopathologique de la gale sarcoptique et de la teigne chez le dromadaire dans le sud marocain. Université Paul Sabatier de Toulouse, Diplome d’Etat Docteur Veterinaire.Google Scholar
- Driscoll, C.A., D.W. Macdonald, and S.J. O’Brien. 2009. From wild animals to domestic pets, an evolutionary view of domestication. PNAS 106: 9971–9978.View ArticleGoogle Scholar
- Epstein, H. 1955. Domestication features in animals as functions of human society. Agricultural History 29(4): 137–146.Google Scholar
- Farah, Z., and A. Fischer. 2004. Milk and meat from the camel. Handbook of products and processing. Zurich: vdf Hochschulverlag AG.Google Scholar
- Faye, B., M.A. Kriska, M. Launois, G. Laveissiére, and T.M. Luong. 2002. Le dromadaire pédagogique. Montpellier: CIRAD.Google Scholar
- Faye, B., S. Grech, and T. Korchani. 2004. Le dromadaire, entre féralisation et intensification. Anthropozoologica 39(2): 7–14.Google Scholar
- Faye, B., H.R. Abdallah, F.S. Almathen, B. Harzallah, and S.E. Al-Mutairi. 2012. Camel biodiversity. Camel phenotypes in Saudi Arabia. FAO.Google Scholar
- Fischer, W. 1965. Farb- und Formbezeichnungen in der Sprache der altarabischen Dichtung. Wiesbaden: Harrassowitz.Google Scholar
- Francis, R.C. 2015. Domesticated. Evolution in a man-made world. New York: W.W. Norton & Company.Google Scholar
- Gauly, M., J. Vaughan, S.K. Hogreve, and G. Erhrdt. 2005. Brainstem auditory evoked potential assessment of auditory function and congenital deafness in llamas (Lama glama) and alpacas (L pacos). Journal of Veterinary International Medicine 19: 756–760.View ArticleGoogle Scholar
- Gauthier-Pilters, H., and A.I. Dagg. 1981. The camel. Its evolution, ecology, behavior and relationship to man. Chicago: The University of Chicago Press.Google Scholar
- Ghabdouane, M., and K. Prasse. 1990. Poeme touaregs de l’Ayr. Copenhagen: CNI Publications.Google Scholar
- Giuffra, E., G. Evans, A. Tornsten, R. Wales, A. Day, H. Looft, G. Plastow, and L. Andersson. 1999. The belt mutation in pigs is an allele at the dominant white (I/KIT) locus. Mammalian Genome 10: 1132–1136.View ArticleGoogle Scholar
- Grandin, T., and M.J. Deesing. 1998. Genetics and animal welfare. In Genetics and the behaviour of domestic animals, ed. T. Grandin, 319–341. San Diego: Academic.Google Scholar
- Householder, D.D. 2003. The genetics of equine coat color. Texas: A&M University, Department of Animal Science.Google Scholar
- Hunn, E. 2011. Ethnozoology. In Ethnobiology, ed. E.N. Anderson, D. Pearsall, E. Hunn, and N. Turner, 83–96. Hoboken: Wiley-Blackwell.View ArticleGoogle Scholar
- Hurn, S. 2012. Humans and other animals. London: PlutoPress.Google Scholar
- International Society of Ethnobiology, 2006. International Society of Ethnobiology Code of Ethics (with 2008 additions). http://www.ethnobiology.net/what-we-do/core-programs/ise-ethics-program/code-of-ethics/code-in-english/.
- Julivert, M. 2003. El Sáhara. Tierras, pueblos y culturas. Valéncia: Universitat de Valéncia.Google Scholar
- Kakar, A.R., K. de Verdier, and M. Younas. 2011. Rapid change of strategy is necessary for development of dromedary camel pastoralism in the Cholistan desert of Pakistan. Pastoralism Research Policy and Practice 1: 3.View ArticleGoogle Scholar
- Köhler-Rollefson, I.U. 1991. Camelus dromedarius. Mammalian Species 375: 1–8.View ArticleGoogle Scholar
- Krätli, S. 2008. Cattle breeding, complexity and mobility in a structurally unpredictable environment: The Wodaabe herders of Niger. Nomadic Peoples 12(1): 11–41.View ArticleGoogle Scholar
- Larson, G., and D.Q. Fuller. 2014. The evolution of animal domestication. Annual Review of Ecology, Evolution, and Systematics 45: 115–136.View ArticleGoogle Scholar
- Leese, A.S. 1927. A treatise on the one humped camel in health and disease. Stamford: Haynes.Google Scholar
- Loubignac, V. 1952. Textes arabes des Zaer (Transcription, traduction, notes et lexique). Paris: Librarie Orientaliste et Américaine.Google Scholar
- Ludwig, A., M. Pruvost, M. Reissmann, N. Benecke, G.A. Brockmann, P. Castanos, M. Cieslak, S. Lippold, L. Llorente, A.-S. Malaspinas, M. Slatkin, and M. Hofreiter. 2009. Coat color variation at the beginning of horse domestication. Science 324: 485.View ArticleGoogle Scholar
- Mahaman, O. 1979. Contribution a l’étude du dromadaire et de sa pathologie infectieuse. Diplome d’etat, Faculté de Médecine et de Pharmacie, University of Dakar.Google Scholar
- Mercer, J. 1976. Spanish Sahara. London: George Allen & Unwin Ltd.Google Scholar
- Migeon, C. 2006. Ma vie de chameau. Magazine Roadbook, 54–62Google Scholar
- Monteil, V. 1952. Essai sur le chameau au Sahrara Occidental, Etudes Mauritaniennes, vol. 2. Saint-Louis du Senegal: Centre IFAN - Mauritanie.Google Scholar
- Morera, M. 1991. La tradición del camello en Canarias. Anuario de Estudios Atlánticos 37: 167–204.Google Scholar
- Musa, H.H., E. Shuiep, and I.E.M. El-Zubeir. 2006. Camel husbandry among pastoralists in Darfur, Western Sudan. Nomadic Peoples 10(2): 101–105.View ArticleGoogle Scholar
- Pacholek, X., R. Lancelot, M. Lesnoff, and S. Messad. 2000a. Performances de croissance des chamelons élevés dans la zone pastorale nigérienne. Revue d Elevage et de Medecine Veterinaire des Pays Tropicaux 53(2): 189–197.Google Scholar
- Pacholek, X., G. Vias, B. Faye, and O. Faugére. 2000b. Elevage camelin au Niger. Référentiel zootechnique et sanitaire. Niamey: Project de Renforcement Institutionnel et Technique de la Filiére Cameline.Google Scholar
- Pape, H. 1990. The inheritance of the piebald spotting pattern and its variation in Holstein-Friesian cattle and in Landseer-Newfoundland dogs. Genetica 80: 115–128.View ArticleGoogle Scholar
- Price, E.O. 2002. Animal domestication and behavior. Wallingford: CABI Publishing.View ArticleGoogle Scholar
- Rook, A., D.S. Wilkinson, F.J.B. Ebling, R.H. Champion, and J.L. Burton, eds. 1998. Textbook of dermatology. 4th ed: Blackwell Scientific Publications.Google Scholar
- Roth, A. 1985. Introduction à l’étude des systèmes de désignation de la couleur dans les parlers arabes du Maghreb in Dictions du prisme. Les couleurs: Désignations et valeurs. Littérature orale arabo-berbère 16–17: 21–65.Google Scholar
- Sandmeyer, L.S., C.B. Breaux, S. Archer, and B.H. Grahn. 2007. Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex. Veterinary Ophtalmology 10: 368–375.View ArticleGoogle Scholar
- Schulz, U., I. Tupac-Yupanqui, A. Martínez, S. Méndez, J.V. Delgado, M. Gómez, S. Dunner, and J. Cañón. 2010. The Canarian camel: A traditional dromedary population. Diversity 2: 561–571.View ArticleGoogle Scholar
- Seitz, J.J., S.M. Schmutz, T.D. Thue, and F.C. Buchanan. 1999. A missense mutation in the bovine MGF gene is associated with the roan phenotype in Belgian Blue and Shorthorn cattle. Mammalian Genome 10: 710–712.View ArticleGoogle Scholar
- Sherratt, A. 1983. The secondary exploitation of animals in the Old World. World Archeology 15(1): 90–104.View ArticleGoogle Scholar
- Shinar, P. 2004. Modern Islam in the Maghrib. Jerulasem: The Max Schloessinger Memorial Foundation, The Hebrew University of Jerulasem.Google Scholar
- Soler, N., C. Serra, J. Escola, and J. Unge. 1999. Sahara Occidental: Pasado y Presente de un Pueblo. Girona: Universidad de Girona.Google Scholar
- Strain, G.M. 1996. Aetiology, prevalence and diagnosis of deafness in dogs and cats. British Veterinary Journal 152: 17–36.View ArticleGoogle Scholar
- Stritzel, S., A. Wohlke, and O. Distel. 2009. A role of the microphthalmia-associated transcription factor in congenital sensorineural deafness and eye pigmentation in Dalmatian dogs. Journal of Animal Breeding and Genetics 126: 59–62.View ArticleGoogle Scholar
- Taine-Cheikh, C. 1989. Le ḥassāniyya: Autopsie d’un dialecte vivant. Matériaux arabes et sudarabiques (GELLAS) Nouvelle série 2: 59–93.Google Scholar
- Taine-Cheikh, C. 2002. Les valeurs du préfixe s- en Hassaniyya et les conditions de sa grammaticalisation, 2002nd ed. Spain: AIDA 5th Conference Proceedings.Google Scholar
- Trut, L., I. Oskina, and A. Kharlamova. 2009. Animal evolution during domestication: The domesticated fox as a model. BioEssays 31: 349–360.View ArticleGoogle Scholar
- Voisset, G. 1989. Enquête sur la littérature mauritanienne: Formes et perspectives. Revue du monde musulman et de la Méditerranée 54: 188–199.View ArticleGoogle Scholar
- Volpato, G., and P. Howard. 2014. The material and cultural recovery of camels and camel husbandry among Sahrawi refugees of Western Sahara. Pastoralism: Research, Policy and Practice 4: 7.View ArticleGoogle Scholar
- Volpato, G., and R. Puri. 2014. Dormancy and revitalization: The fate of ethnobotanical knowledge of camel forage among Sahrawi nomads and refugees of Western Sahara. Ethnobotany Research & Applications 12: 183–210.View ArticleGoogle Scholar
- Volpato, G., D. Rossi, and D. Dentoni. 2013. A reward for patience and suffering - ethnomycology and commodification of desert truffles among Sahrawi refugees and nomads of Western Sahara. Economic Botany 67(2): 147–160. doi:10.1007/s12231-013-9234-7.View ArticleGoogle Scholar
- Wardeh, M.F. 2004. Classification of the dromedary camels. Journal of Camel Science 1: 1–7.Google Scholar
- Webb, A.A., and C.L. Cullen. 2010. Coat color and coat color pattern-related neurologic and neuro-ophthalmic diseases. Canadian Veterinary.Journal 51: 653–657.Google Scholar
- Wilkins, A.S., R.W. Wrangham, and W.T. Fitch. 2014. The “domestication syndrome” in mammals: A unified explanation based on neural crest cell behavior and genetics. Genetics 197: 795–808.View ArticleGoogle Scholar
- Wilson, R.T. 1978. Studies on the livestock of Southern Darfur, Sudan. Tropical Animal Health and Production 10: 19–25.View ArticleGoogle Scholar
- Wilson, R.T. 1984. The camel. London: Longman.Google Scholar
- Wolf, E.R. 1982. Europe and the people without history. Los Angeles: University of California Press.Google Scholar
- Woolf, C.M. 1991. Common white facial markings in bay and chestnut Arabian horses and their hybrids. Journal of Hered. 82: 167–169.View ArticleGoogle Scholar
- Zeder Melinda A. 2012. Pathways to animal domestication. Biodiversity in agriculture: Domestication, evolution, and sustainability:227.Google Scholar