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Domestication and early history of the horse

Domestication and early
history of the horse
Marsha A. Levine
Before the development of firearms, the horse was
crucial to warfare and before the invention of the
steam engine, it was the fastest and most reliable form
of land transport. Today its importance has scarcely
diminished in parts of South America, Asia, Africa
and Eastern Europe, and even elsewhere it is of great
economic importance to sport and leisure industries.
Nevertheless, in spite of intensive investigations over
many years, researchers know very little about the
origins of horse domestication and the evolution of
horse husbandry.
The origins of horse domestication
Throughout the course of the twentieth century a
variety of theories have been developed purporting
to explain where, when and for what purposes the
horse was first domesticated. The basic positions can
be summarized as, that it was first domesticated:
rduring the Neolithic, Eneolithic or Early Bronze Age
(Table 1.1);
rfor meat, riding or traction;
rin Ukraine, Kazakhstan, Eastern Europe or Western
rpossibly in response to contacts with the Near East;
rat a single locus or at a number of different loci,
more or less simultaneously.
In some situations it is, of course, easy to show
how horses had been used in ancient times. For
example, the horses found in some of the Altai
Early Iron Age kurgan burials (Figure 1.1) – such
as Pazyryk, Bashadar and Ak-Alakha – as a result
of their burial in permafrost, were accompanied by
well-preserved equipment such as bridles, saddles
and harnessing (Rudenko, 1970; Polos’mak, 1994).
Because of Rudenko’s publication The Frozen Tombs
of Siberia, Pazyryk is especially well known, but many
other Early Iron Age sites from the Ukraine and south
Siberia are equally spectacular. Many of the richer
graves contained objects made of gold and silver –
for example, jewellery, vessels, harness ornaments,
weapons and belt buckles. Carpets, wall hangings,
The Domestic Horse: The Origins, Development, and Management of its Behaviour, ed. D. S. Mills & S. M. McDonnell. 5
Cambridge University Press. CCambridge University Press 2005.
6M. A. Levine
Figure 1.1. Map showing
locations of Dereivka, Botai
and Early Iron Age Altai sites:
Ak-Alakha, Bashadar and
Table 1.1. Chronology of the west Eurasian steppe
Approximate Dates (bc) Period
900–300 Early Iron Age
1000–900 Transition to Early Iron
1800/1700–1200/1000 Late Bronze Age
2000/1900?–1800/1700 Middle Bronze Age
3000/2900 (2750?)–2300/1900? Early Bronze Age (EBA)
3500/3400–3000/2900 (2750?) Final Eneolithic –
beginning of EBA
4800/4700?–3500/3400 Eneolithic
6000–4800/4000 Neolithic
clothing made of felt, furs and even silk from China
have also been recovered (Cahen-Delhaye, 1991). It
is intriguing to note that the jointed snaffle bit was in
wide use in central Eurasia during the Early Iron Age
(first millennium bc).
At most sites, however, especially those dating from
the period when horses were first domesticated for
riding and traction, determining whether an animal
was domesticated is much more difficult, sometimes
impossible. Organic materials such as leather and
wood are only very rarely recoverable from the
archaeological record. In unfavourable soil conditions
even bone is eventually destroyed. Moreover, not only
is it possible to ride a horse without the use of a sad-
dle or bridle, but also, during the early stages of horse
domestication, it is likely that they were usually rid-
den that way.
In recent years two sites have come to the fore
in debates concerning the origins of horse domesti-
cation: Dereivka and Botai. Dereivka, an Eneolithic
Ukrainian settlement site, has been central to the
problem of the origins of horse domestication,
because for the past three decades it has been
regarded as the site with the earliest evidence of horse
husbandry (e.g. B ¨
ok ¨
onyi, 1978; Bibikova, 1986b;
Telegin, 1986; Mallory, 1989; Anthony & Brown,
1991; Gimbutas, 1991). More recently Botai, an Ene-
olithic settlement site from Kazakhstan, has also been
associated with this question (Brown & Anthony,
1998) (Figure 1.1). Because of the enormous num-
bers of horse bones found at Botai, it was inevitable
that this site would be considered in such discussions.
1. Domestication and early history of the horse 7
However, upon further examination such as that
below, it should be clear that the evidence backing
the claims for both sites is deeply flawed.
Types of evidence for the origins of
horse domestication
Two types of evidence are referred to in discussions of
the origins of horse domestication: direct and indirect.
Direct evidence relates to artistic, textual and funerary
evidence, where there is virtually no doubt both that
the horses were caballine and that they were ridden
or used for traction.
Indirect evidence is inferred from characteristics of
bones and artefacts. It includes evidence derived from
analytical methods such as population structure, bio-
geographical distribution and artefact studies. It is
invariably the case that any one pattern manifested
by these types of data could have more than one
explanation. On its own, no one type of data can
provide satisfactory evidence of horse domestication.
Indirect evidence must have corroboration from as
many directions as possible.
Some types of indirect evidence are frequently con-
fused with direct evidence. That is, data – whose asso-
ciation with horse husbandry is only inferred – are
treated as if they could only be explained by horse
domestication. Eneolithic bit wear and cheekpieces
are examples of false direct evidence.
Direct evidence
The earliest unambiguous direct evidence – that is,
dateable textual and artistic evidence – for horse
domestication probably only dates back to the end
of the third millennium bc (Postgate, 1986; Zarins,
1986; Piggott, 1992; Kuz’mina, 1994a,b, 1996;
Littauer & Crouwel, 1996). Evidence of horses in
graves, accompanied by artefacts unambiguously
associated with riding or traction is even more recent,
dating to probably no later than the beginning of the
second millennium bc (Postgate, 1986; Piggott, 1992;
Kuz’mina, 1994a,b, 1996; Anthony, 1995; Littauer
& Crouwel, 1996). By the middle of the second mil-
lennium bc horses were widely used to pull char-
iots – for example, in the Near East, Greece, and
on the Eurasian steppe (Piggott, 1992; Littauer &
Crouwel, 1996; Renfrew, 1998). There is apparently
no reliable textual or artistic evidence for horse rid-
ing earlier than the end of the second millennium bc
(Renfrew, 1987, 1998; Piggott, 1992). There are
earlier representations of people riding equids in the
Near East. However, because of the extreme difficulty
of distinguishing artistic representations of horses
from those of asses, it is impossible to identify the ear-
liest evidence for horse riding itself (Piggott, 1992). It
is highly improbable, however, that traction horses
could have been herded either on foot or from a vehi-
cle. Therefore it seems almost certain, as far as the
horse is concerned, that riding would have preceded
One interpretation of this evidence is that the horse
was first domesticated for traction around the end
of the third millennium bc and for riding a little
earlier (Khazanov, 1984; Renfrew, 1987; Kuz’mina,
1994a,b). However, it is almost certain that horse hus-
bandry must have developed well before its earliest
unambiguous manifestations in art and burial ritual.
As Piggott pointed out, these representations are not
merely portrayals of everyday life, they are closely
connected with the delineation of power and prestige
(Piggott, 1992, p. 69). If horse riding, at its inception
and during its early development, did not have high
status, it would have been unlikely to have been rep-
resented in art or burials. It might not, in fact, have
left any direct evidence at all. This evidential ‘invis-
ibility’ seems to suggest that, whatever its practical
value, the horse was of little or no political or social
significance until the end of the third millennium bc.
This point of view is, of course, in direct conflict with
the picture of horse-powered migration and warfare
during the Eneolithic and Early Bronze Age proposed
by Gimbutas (e.g. 1970; 1991), and supported by
many others (Telegin, 1986; Mallory, 1989; Anthony,
False direct evidence
Four types of evidence, conventionally accepted as
proof of horse domestication, fall into the category
of false direct evidence:
rHorse-head sceptres.
rHorse burials not associated with tack.
rBit wear.
Horse-head ‘sceptres’ or ‘maces’ (Figure 1.2)
Horse-head ‘sceptres’ (Telegin, 1986; Gimbutas,
1991) or ‘maces’ are found in Eneolithic burials from
the Volga to the Lower Danube. Only a few have
8M. A. Levine
Figure 1.2. Horse-head ‘sceptres’:
(1) Suvorovo II, Kurgan 1, Burial 7;
(2) Kasimcea; (3) Khutor
Shlyakhovsky, Kurgan 3 Burial 3
(from Rassamakin, 1999, figure 3.14;
cMcDonald Institute).
1. Domestication and early history of the horse 9
more than a passing resemblance to horses’ heads and
those are found west of the Dneiper, mainly in the
Balkan and Lower Danube regions (Telegin, 1986;
ausler, 1994a). These sculptures are conventionally
regarded as symbols of the power wielded by the male
occupants of the graves in which they were found
(Anthony, 1991, p. 267). It was, however, the archae-
ologists not the Eneolithic people who described them
as ‘maces’ or ‘sceptres’. Their association with power
is largely based upon the fact that they are made of
exotic stone such as porphyry. The markings carved
on some of the sculptures, which have been described
as depictions of harnessing, are too schematic to be
used as evidence of such (Anthony, 1991). The sculp-
tures are not, in fact, found with any direct or even
indirect evidence of horse husbandry.
Horse bones in human burials
Mallory (1981) and Anthony and Brown (2000),
describe cemeteries from the Pontic-Caspian region in
which horse bones are associated with human buri-
als from Eneolithic (Khvalynsk) and Early Bronze
Age (Yamnaya and Catacomb) cultures (Chernykh,
1992; Mallory, 1981, 1989; Y. Y. Rassamakin, pers.
comm.). Domestic animal bones are relatively rare
in graves from these periods and both ovicaprids
and cattle are much more frequently found than
horses (Mallory, 1981). Cattle skulls from these cul-
tures are found in human burials with wagons, but
horses are not. Neither are they associated with rid-
ing tack or harnessing (Mallory, 1981; Piggott, 1992;
Renfrew, 1998). Complete horse skeletons are very
rarely found in these burials. Often only a few or even
only one horse bone will be included (Mallory, 1981;
Anthony & Brown, 2000). The skull, teeth or jaw
are the most frequently represented anatomical ele-
ments, followed by foot bones. However, skull and
foot bones are rarely found together. According to
Mallory (1981), there is no correlation between horse
bones and other symbols of wealth or ranking in these
That Eneolithic and Early Bronze Age peoples went
to the trouble of burying horses attests to their sym-
bolic significance, but it cannot be taken as evidence
of domestication. Hares were also found in Yamnaya
and Catacomb culture graves, but no one claims,
on that basis, that they were domesticated (Mallory,
Cheekpieces (Figure 1.3)
Perforated antler tines, found at Dereivka and a few
other Eneolithic or Early Bronze Age sites, have been
widely interpreted as cheekpieces and thus taken as
evidence for Eneolithic horse riding (e.g. Mallory,
1981, 1989; Anthony, 1986, 1991; Telegin, 1986).
This identification has been questioned in recent years
on a number of grounds (Levine, 1990; Uerpmann,
1990; Dietz, 1992; H¨
ausler, 1994b; Rassamakin,
1999). That is, these objects have never been found in
place on a horse’s skull; rarely are they even found
in association with horses. There is no contextual
support for the notion that they were bridle cheek-
pieces. Those at Dereivka were found in association
with other bone tools, pottery, and flaked and ground
stone tools (Telegin, 1986). Moreover, their form is
so general that they could have served a variety of
Bit wear
Although bit wear had been described earlier by
ok ¨
onyi (1968) and Clutton-Brock (1974), its use
to investigate the origins of horse riding, has been
pioneered by Anthony and Brown (1991; Brown &
Anthony, 1998). They define bit wear as: ‘the damage
that occurs on the occlusal...surfaces of the second
premolar teeth . . . , particularly the lower second pre-
molars . . . , when a horse chews the bit’ (Brown &
Anthony, 1998, p. 331). They state that the pattern
of wear that they define as bit wear is direct evidence
for horse riding or traction.
Useful though it certainly is, their approach has a
number of problems and limitations which they have
glossed over:
rBrown and Anthony (1998) describe two types of
bit-wear evidence: microscopic and macroscopic.
The microscopic evidence is problematic in the
archaeological context, since it is likely to be lost
under most burial conditions. Even at Botai, an
Eneolithic settlement site, where tooth preservation
was very good, Brown and Anthony were not able
to find any microscopic wear evidence.
rBit wear would seem, by definition, to provide direct
evidence for the use of the horse for transport. How-
ever, Anthony and Brown have not demonstrated
that the wear pattern that they describe as bit wear
could not have had other causes (Anthony & Brown,
1991; Brown & Anthony, 1998). Indeed, there is
10 M. A. Levine
Figure 1.3. ‘Cheekpieces’: (1)–(5) Dereivka; (6) Mayaki;
(7) Vulkaneshty (from Rassamakin, 1999, Figure 3.55;
cMcDonald Institute).
1. Domestication and early history of the horse 11
evidence that such wear can result from abnormal
occlusion (Levine et al., 2002; A. von den Driesch,
pers. comm.). Moreover, the median bevel of the
domestic population is only 0.5 mm greater than the
maximum bevel of their comparative feral sample.
rBrown and Anthony (1998) have recently described
a series of experiments they carried out to prove:
(1) that a metal-bitted horse, which is ridden reg-
ularly, will have bit wear; and (2) that soft bits –
leather, rope and bone – will also cause bit wear.
However, the results of both tests were, in fact,
inconclusive. Most significantly, after 150 hours of
riding, none of the soft-bitted horses showed a sig-
nificant bevel.
Two conclusions can be drawn from this: (1) that
it has not been demonstrated that soft bits can cause
archaeologically visible bit wear; and (2) that it has
not been proved that a bone bit could result in ‘signifi-
cant’ bit wear. Bit-wear studies are useful, but they do
not on their own provide conclusive or direct evidence
of the use of the horse for transport.
Indirect evidence
None of the genuinely direct types of evidence reach
back far enough to be informative about the nature of
human–horse relationships during the Eneolithic and
Early Bronze Age, the period upon which arguments
about the origins of horse domestication focus. It is
therefore necessary to use indirect evidence to recon-
struct relationships that took place probably at least
1000 years before the earliest direct evidence for horse
Inappropriate use of indirect evidence
Much of the indirect evidence, that is, evidence based
upon inference and interpretation, has been unsatis-
factory. Some important problems include:
rconfusion of intensification with domestication;
ruse of a single type of evidence as proof of domesti-
rinadequate testing of theories.
As most of these points have been discussed in detail
elsewhere (Levine, 1990, 1993, 1999a), some of the
central issues will only be briefly reviewed here.
Criteria used as evidence (e.g. B ¨
ok ¨
onyi, 1984;
Bibikova, 1986a; Telegin, 1986) that horses from
Dereivka were domesticated include:
rabsence of old horses;
rpresence of a high proportion of male horse skulls;
rpresence of objects identified as bridle cheekpieces;
rresults of a morphological analysis comparing the
Dereivka horses with other equid material;
rtheir association with other domesticates;
rrelatively high percentage of horse bones and teeth
in the deposit.
These are not good criteria for horse domestica-
tion. In fact, on the basis of archaeological, ethno-
graphic and ethological comparisons, the absence of
old individuals is much more likely to indicate hunting
than herding. Males would outnumber females either
if bachelor groups or stallions protecting their harems
were targeted in the hunt. Morphological studies have
involved very small and disparate samples and pro-
duced contradictory results. The association of horses
with other assumed domesticates is not evidence of
horse domestication. In any case, they were also asso-
ciated with wild animals. In fact, the most important
criterion used was the relatively high proportion of
horse bones and teeth present at the site (e.g. B ¨
ok ¨
1984; Petrenko, 1984; Bibikova, 1986b; Matyushin,
1986; Telegin, 1986; Gimbutas, 1988; Dergachev,
1989; Makarova & Nurumov, 1989; Mallory, 1989;
Anthony, 1991; Anthony & Brown, 1991). However,
throughout the Palaeolithic the archaeological record
shows that horse meat was almost always an impor-
tant component of the human diet.
Uerpmann claims that: ‘Reduction in size on the
one hand and increase in variability on the other are
classic indicators of domestication’ (Uerpmann, 1990,
p. 127). However, horse populations have exhibited
this kind of variability throughout the Pleistocene and
into the post-Pleistocene. Environmental change, geo-
graphical isolation and genetic drift are all connected
with size change.
Additionally any morphological changes brought
about by domestication would almost certainly have
appeared too late to signal its earliest stages. In any
case, there are no indisputable osteological differences
between wild and domesticated horses.
Biogeographical range is also problematic as evi-
dence of early horse domestication. During the Upper
Pleistocene (c. 130 000–10 000 bp; Otte, 1996) wild
caballine horses (the ancestors of both the domestic
horse and the Przewalski’s horse) were found through-
out most of northern Eurasia, ranging from 75Nto
12 M. A. Levine
35N and from 130Eto10
W (Eisenmann, 1996).
During the following Holocene period the archaeo-
logical evidence for horses, particularly in Western
and central Europe, is much sparser – fewer remains
were found at fewer sites (Clutton-Brock, 1992). This
has been interpreted as meaning that the horse had
become extinct throughout large parts of its original
range. The natural Holocene range of the horse was
thus taken to comprise Eastern Europe and central
However, horse numbers in western and central
Europe during this period are greatly underestimated
for a variety of reasons. For one thing, relatively few
faunal assemblages, dating to this period, have been
submitted to detailed analysis. Additionally, when
horse remains are identified outside their expected
geographical range, it is frequently assumed that they
must have been either domesticated or intrusive from
later levels (e.g. Grigson, 1993; Curci & Tagliacozzo,
1995). Such material is frequently excluded from fau-
nal reports (K. Boyle, pers. comm.).
Recent research suggests that the natural distribu-
tion of the Holocene horse was much wider than had
formerly been believed. Neolithic remains from puta-
tively wild horses have, for example, been found in
Sweden, Denmark, the Netherlands, France, Spain,
Italy, Germany, Switzerland, Hungary and Serbia –
in addition to Ukraine, Russia and Kazakhstan
(Azzaroli, 1985; Groves, 1986; Zarins, 1986; Cabard,
1987; Clason, 1988; Schibler & Steppan, 1999).
Because the origins of the earliest domestic horses
are not known, it is not certain that all these horses
were, in fact, wild (Uerpmann, 1990; Benecke, 1999).
Moreover, it should not be assumed that the absence
of horses from archaeological assemblages is evidence
that they were not present. They might well have been
available, but not hunted for either logistic or cultural
The belief that the horse became extinct in western
Europe and relatively rare in central Europe underlies
the assumption that its earliest domestication must
have taken place in eastern Europe or central Asia.
However, the fact that wild horses were more com-
mon in those regions does not prove that they were
first domesticated there.
Population structure analysis
The study of population structure, that is, the age and
sex structure of an archaeozoological assemblage, can
offer useful insights into the nature of ancient rela-
tionships between people and animals. Each pattern
of behaviour or method of exploitation is character-
ized by its own typical, though not necessarily unique,
population structure. These structures can be used as
models to which the archaeological data can be com-
pared. The raw material for this analytical method is
the aged teeth from archaeological deposits. Determi-
nation of an individual’s age at death is based upon
measurements of crown height and assessments of
eruption and wear (Levine, 1982, 1999b).
Population structure of wild horses The anchor for
this method is the population structure of the wild
horse. The natural reproductive unit of the horse is
the family group, composed of a stallion, his mares
and their young up to the age of about two to four
years (Klingel, 1969, 1974; Berger, 1986; Boyd and
Keiper Chapter 4). It may comprise from 2 to 17 indi-
viduals. The average number of mares is around two
to four. The stallion normally starts his own family
group at the age of five or six years, although he might
not be successful at holding one against attacks from
other males until he is older. The second natural horse
social unit is the bachelor group, composed entirely
of males, too young or too old to belong to a family
group. Its average size is typically two to four horses.
The Attritional Assemblage Model (Figure 1.4a) The
mortality distributions for natural attrition, scaven-
ging, coursing on foot and livestock husbandry, where
meat production is of secondary importance, are all
similar to the Attritional Model. Mortality is low for
adults during their reproductive years, and high for
juveniles and senescent individuals (Caughley, 1966).
The Carnivorous Husbandry Model (Figure 1.4b) A
mortality curve resembling the Carnivorous Hus-
bandry Model might be generated if the slaughter of
individuals at around the age of two to four years
were superimposed upon the pastoral nomadic attri-
tional pattern (Levine, 1999a). A very similar age
distribution was produced from data provided by
Yuri Shavardak, a semi-traditional horse herder from
northern Kazakhstan.
The Life Assemblage or Catastrophe Model (Figure
1.4c) The Life Assemblage Model is representative
1. Domestication and early history of the horse 13
Figure 1.4. Age structure models. (a) The Attritional
Assemblage Model. (b) The Carnivorous Husbandry Model.
(c) The Life Assemblage or Catastrophe Model. (d) Family
Group Model. (e) Bachelor Group. (f) The Stalking Model.
14 M. A. Levine
Figure 1.5. Archaeological age structures. (a) Pooled Western
European, Upper Pleistocene archaeological assemblages.
(b) Age structure at Botai (Bot) and Dereivka (Der).
either of a living population, a catastrophe assem-
blage, or an assemblage in which all age classes are
represented as they would be in the living popula-
tion because of completely random sampling (Levine,
1983). Herd driving, or any other non-selective hunt-
ing technique, should produce this mortality pattern
or that of the Family Group Variant.
Social group models (variants of the Life Assem-
blage Model) The main difference between the Life
Assemblage Model and the Family Group Model
(Figure 1.4d) is the relatively low proportion in the lat-
ter of individuals three to six years of age, marking the
absence of bachelor males (Levine, 1983). This is the
kind of pattern produced by the Western European,
Upper Pleistocene material previously studied –
particularly when adjusted to compensate for the
probable under-representation of immature animals1
Figure 1.5a.
Figure 1.4e illustrates a hypothetical Bachelor
Group age distribution. Its most archaeologically visi-
ble characteristic would be the absence of any individ-
uals younger than about two years of age. Bachelor-
group hunting might, in the archaeological context,
be indistinguishable from the stalking of prime adults
(Levine, 1983).
The Stalking Model (Figure 1.4f) Stalking is a
selective hunting technique in which the prey is
approached by stealth and killed. Hunting mainly
prime adults should also produce this distribution
(Levine, 1983).
Botai and Dereivka (Figure 1.5b) The age distribu-
tions for both Botai and Dereivka fit hunting mod-
els, but the differences between them strongly sug-
gest that different hunting techniques were used. For
example, although the mortality rates for both Botai
and Dereivka are very similar from the age of eight
years and onwards, the rates for younger horses are
distinctly divergent. At Dereivka mortality is concen-
trated between the ages of five to eight years, while at
Botai it extends at least back to the age of three years.
The difference is even greater when the distribution is
adjusted. While the horses from Dereivka were proba-
bly stalked, it seems that those from Botai were killed
in herd drives. This conclusion is supported by the
very different sex ratios at the two sites. At Dereivka
the ratio of males to females is 9:1, which is compati-
ble with stalking; while at Botai the ratio is almost 1:1,
which is best explained by a non-selective technique,
such as herd driving (Levine, 1999b).
Palaeopathological analysis provides one of the most
promising approaches for the study of the evolution of
horse husbandry. The results of a recent palaeopathol-
ogy project carried out by the author with Leo Jeffcott
and Katherine Whitwell indicate that the types and
incidences of certain abnormalities of the caudal
1. Domestication and early history of the horse 15
Figure 1.6. Deposition of spurs of new bone on the ventral
and lateral surfaces of the vertebral bodies adjacent to the
intervertebral space. Ak-Alakha 5, kurgan 3, horse 4; thoracic
vertebra 14.
thoracic vertebrae could be connected with riding
(Levine, 1999b; Levine et al., 2000). Four Early Iron
Age, Scytho-Siberian skeletons from Ak-Alakha 5
(Altai), dated fifth to third century bc, were found
buried with bits between their teeth. Although their
bones were well preserved, burial conditions were
not good enough for the survival of saddles. How-
ever, the context of the burials suggests that they were
riding horses. Most of the anatomical elements from
all four Early Iron Age horses are normal. However,
all of them have similar abnormalities of the caudal
thoracic vertebrae:
(1) Deposition of spondylotic spurs of new bone on
the ventral and lateral surfaces of the vertebral
bodies adjacent to the intervertebral space (Figure
Figure 1.7. Overriding or impinging dorsal spinous processes.
Ak-Alakha 5, kurgan 3, horse 1; thoracic vertebrae 14–18,
lumbar vertebra 1.
(2) Overriding or impinging dorsal spinous processes
(Figure 1.7).
(3) Horizontal fissures through the epiphysis
(Figure 1.8).
(4) Periarticular osteophytes: the deposition of new
bone on and above adjacent articular processes
between vertebrae (Figure 1.9).
This work is still in progress, but the initial results
of comparisons of the Early Iron Age horses, which
wore pad saddles, with free-living modern Exmoor
ponies, which were never saddled, and with Medieval
Turkic horses (Ak-Alakha 1, Altai), which wore frame
saddles, strongly suggest that these abnormalities, as
a complex, are associated with the use of pad sad-
dles and, most probably, with riding bareback (Levine
et al., 2000; Levine et al. in press.) (Tables 1.2a–c).
These types of abnormalities are entirely absent
from the sample of vertebrae studied from the
Eneolithic site, Botai (Figure 1.10), supporting the
results of the population structure analysis, which
concluded that the horses from Botai were wild.
Unfortunately the vertebrae from Dereivka had all
been discarded before they could be examined.
Taming and domesticating horses
Despite our ignorance of the origins of horse domesti-
cation, it is nevertheless possible – using archaeolog-
ical, ethnographic and ethological data – to consider
how horse husbandry might have originated.
16 M. A. Levine
Figure 1.8. Horizontal fissure through the epiphysis.
Ak-Alakha 5, kurgan 3, horse 4, thoracic vertebra 14.
According to Juliet Clutton-Brock, ‘A tame animal
differs from a wild one in that it is dependent on man
and will stay close to him of its own free will’ (Clutton-
Brock, 1987, p. 12)). Aboriginal hunter–gatherers and
horticulturists throughout the world are known to
tame all kinds of wild animals to keep as pets. There
is no reason to think that this would not have been the
case at least from the time of the earliest anatomically
modern Homo sapiens and, when the need arose, tam-
ing would probably have been the first step towards
domestication (Galton, 1883; Clutton-Brock, 1987;
Serpell, 1989). Wild horses, particularly as foals, can
be captured and tamed and, as such, ridden or har-
nessed and, at the end of their lives, if necessary,
slaughtered and eaten. During historical times both
the North American Plains tribes and the Mongols
used the arkan, lasso or herd drive to capture wild or
Figure 1.9. Periarticular osteophytes: the deposition of new
bone on and above adjacent articular processes between
vertebrae. Ak-Alakha 5, kurgan 3, horse 4; thoracic
vertebra 16.
feral horses to eat or to tame them (Levine, 1999a).
Horse taming was regarded as a skill most success-
fully carried out by specialists, whose most important
tool was their intimate knowledge of horse behaviour.
On this basis, a possible scenario for the development
of horse domestication may be proposed.
As a working hypothesis, the author would like to
suggest that horse taming probably first arose as a by-
product of horse hunting for meat. Orphaned foals,
captured between the ages of perhaps two months
and one year, or possibly somewhat older – when
they were no longer dependent upon their mother’s
milk – would sometimes have been adopted and raised
as pets. Eventually, and perhaps repeatedly, the dis-
covery was made that these pets could be put to
work. This knowledge could have been acquired and
lost many times from the Pleistocene onwards. But it
1. Domestication and early history of the horse 17
Table 1.2a. Description of thoracic vertebrae 11–19 abnormalities: Early Iron Age horses
Ak-Alakha 5 (Altai)
Horse number 1 2 3 4
Age (years) 16+10–15 101
Sex Male Male Male Male (possible gelding)
Number of thoracic vertebrae 18 19 18 18
(1) Osteophytes/spondylosis on
the ventral and lateral
surfaces of the vertebral
bodies adjacent to the
intervertebral space
T11 to 18 Increasing from T11
to T14 (11 & 12
caudal; 13 & 14
caudal +cranial)
T14, 17, 18 strongly
developed; T15
weakly developed
T13 to 15 most strongly
developed, but extends
to T17
(2) Impinging or overriding
spinous processes
T16–18 (possibly
T15 also)
T14–15 probably;
T15–19 possibly
Unclear because of
poor preservation
T10–12 probably
(3) Horizontal fissure through
T13 and 15,
T13 and 14, (most
developed on
T14), caudal
T14, caudal; T18,
T13 and 14, (most
developed on T14),
(4) Periarticular changes T16–17 small
T15–18 small
T17, 18 small
Exostoses, increasingly
from T14 to T17, then
aAt T16–T17 and, to a lesser extent at T15–T16, these changes were pronounced and extended dorsally to involve the adjacent
vertebral arches and lower regions of the spinous processes. This had not, however, resulted in the fusion of the vertebrae.
Table 1.2b. Description of thoracic 11 to 19
abnormalities: modern Exmoor ponies
Horse number 97/2 97/7
Age (years) 12 27
Sex Female Female
Number of thoracic
18 18
(1) Osteophytes/spondylosis
on the ventral and
lateral surfaces of the
vertebral bodies
adjacent to the
intervertebral space
Not present Sightly developed,
(2) Impinging or overriding
spinous processes
Not present Not present
(3) Horizontal fissure
through epiphysis
Not present Not present
(4) Periarticular changes Not present T11–18 small
was, apparently, only during the Holocene – possibly
between the Neolithic and the Early Bronze Age – that
it began to influence human social developments.
Initially the difficulties involved in keeping cap-
tured wild horses alive would have set limits to
their impact – as work animals – on human society.
Furthermore, considering the problems encountered
by modern collectors trying to breed Przewalski’s
horses, it seems likely that horse-keeping would have
had to have been relatively advanced before con-
trolled breeding over successive generations, and thus
domestication, would have been possible. As Boyd
and Houpt point out: ‘Failure to consider the typical
social organization of the species can result in prob-
lems such as pacing, excessive rates of aggression,
impotence and infanticide’ (Boyd & Houpt, 1994,
p. 222). Thus, in order to breed wild horses success-
fully in captivity, their environmental, nutritional and
social requirements must be met. Again quoting Boyd
and Houpt (1994, p. 226):
In zoos, juvenile male Przewalski’s horses should be left in their
natal bands for at least a year so that they can observe mat-
ing behaviour. They should be placed in bachelor herds when
removed from the natural band, and not given harems until they
are at least four or five years of age. The first mares placed with
the stallion should be younger than he and the harem size should
be kept small until the stallion gains age and experience.
The cognitive and logistical difficulties involved in
creating such an environment at the time of the earliest
horse domestication should not be underestimated.
Although it is not possible to know for sure that the
ancestor of the domestic horse would have been more
amenable to captive breeding than the Przewalski’s
18 M. A. Levine
Table 1.2c. Description of thoracic 11 to 19 abnormalities: Medieval Turkic horses
Ak-Alakha 1 (Altai)
Horse number 1 2
Age (years) 11 years 10.5 years
Sex male male
Number of thoracic vertebrae 18 18
(1) Osteophytes/spondylosis on the ventral and
lateral surfaces of the vertebral bodies
adjacent to the intervertebral space
T14, small ventral spondylotic spur Not present
(2) Impinging or overriding spinous processes Spines crowded together and T13–16 have
been touching, no significant overriding
Not present
(3) Horizontal fissure through epiphysis Not present Not present
(4) Periarticular changes Slight erosion and pitting of articular facets
between T14 & 15, T15 & 16, T17 &
Some fairly insignificant bony
thickening on the processes
between T13 & T14, T14 &
Figure 1.10. Botai caudal thoracic vertebrae.
horse, it seems unlikely. That capturing wild horses
and stealing tamed or domesticated ones was regarded
by the Plains tribes as preferable to breeding them
supports the scenario proposed here. If it is correct,
it seems likely that there would have been a relatively
long period of time when new horses would have been
recruited from wild populations. This could have been
carried out by trapping, driving and chasing, as docu-
mented for the Mongols and North American Plains
tribes (Levine, 1999a).
Consideration of the ethological and ethnographic
evidence further suggests a scenario in which the ini-
tial taming and perhaps the earliest breeding of the
domestic horse progenitors could have been confined
to the ‘horse whisperers’ of the ancient world (Levine,
1999a). That the breeding of domestic horses today is
so straightforward seems likely to be the consequence
of the selective breeding of particularly amenable
beasts some thousands of years ago. As Hemmer
(1990, pp. 187–8) points out, behavioural change is
an inherent part of the process of domestication:
The environmental appreciation of the domestic animal is
innately reduced when compared to that of wild animals. This
is expressed in a lower intensity or even disappearance of par-
ticular patterns of behaviour ...Asingular intensification of
sexual activity contrasts with the general attenuation of other
Such behavioural changes, in fact, probably do
have a genetic basis (Hemmer, 1990; Hausberger and
Richard-Yris Chapter 3). Given the complexity of
both horse and human behaviour, as described above,
it seems rather unlikely that these kinds of changes
would have taken place many times in many places.
However, once controlled breeding was established
and the horse domesticated, it is likely that its value
as a work animal would have been appreciated and its
1. Domestication and early history of the horse 19
population could have increased quite rapidly (Berger,
This leads to a hypothesis that horse domesti-
cation would have taken a relatively long time to
develop and might well have depended upon chance
genetic changes that would have predisposed some
horses to breed in captivity. Another possibility is
that the human understanding of horse behaviour
might have developed to such a degree that horses
finally would have been able to reproduce in captiv-
ity. Perhaps the most likely scenario is that the human
and equine parts of the equation would have evolved
Mitochondrial DNA and the origins of
horse domestication
At first glance the above scenario might appear to con-
flict with the most recent evidence from mitochondrial
DNA (mtDNA) research. All three recent investiga-
tions of horse mtDNA have revealed that, in contrast
to cattle and goats, the domestic horse is characterized
by high genetic diversity (Jansen et al., 2002; Hall
Chapter 2). Lister et al. (1998) explains this with a
model that envisages: ‘domestic horses having arisen
from wild stock distributed over a moderately exten-
sive geographical region, large enough to have con-
tained within it considerable pre-existing haplotype
diversity’ (Lister et al., 1998, p. 276). Vil`
aet al. (2001)
propose two hypotheses: (1) the ‘selective breeding
of a limited wild stock from a few foci of domestica-
tion’; and (2) ‘a large number of founders recruited
over an extended time period from throughout the
extensive Eurasian range of the horse’ (Vil`
aet al.,
2001, p. 474). They finally reject the first explanation
and choose a modified version of the second: ‘initially,
wild horses were captured over a large geographic
area and used for nutrition and transport’ (Vil`
aet al.,
2001, p. 477).
The study by Jansen et al. (2002), with its much
larger sample of 652 horses, expands upon these
results. The analysis revealed that at least 77 success-
fully breeding mares were recruited from the wild.
Moreover, several of the phylogenetic clusters cor-
respond to breeds or geographic areas. This study
confirms that the Przewalski’s horse mtDNA types
are closely related and are not found in any other
breed and that this animal is very unlikely to be
ancestral to the domestic horse. Jansen et al. (2002)
also examine both the ‘restricted origin’ and ‘multiple
founder’ hypotheses. They conclude that the present
mtDNA diversity could not have originated from a
single wild population. However, they point out that
this finding does not necessarily support the ‘multiple
founder’ hypothesis. Taking archaeological, etholog-
ical, ethnographic and genetic evidence into account,
at present the most likely scenario for the origin of
horse domestication is one in which the knowledge
of horse-breeding and the concomitant spread of the
horse diffused from an origin, localized both spatially
and temporally. The overall data seem to suggest that,
as the knowledge of horse-breeding spread, additional
horses from wild populations were incorporated into
the domestic herds, thus forming the regional mtDNA
clusters. It must be said, however, that this field of
study is only at a very early stage. Further research –
archaeological, palaeopathological and genetic – hold
great promise for our understanding of the origins
of horse domestication and the evolution of horse
I would like to thank Yuriy Rassamakin and Yakov
Gershkovich for help with the archaeological chronol-
ogy and Katie Boyle and Peter Forster for com-
ments about the text. I am grateful to Dora Kemp
who helped to prepare the illustrations for this chap-
ter. I would like to thank the McDonald Institute
for Archaeological Research for allowing me to use
figures 3.14 and 3.55 from Rassamakin (1999). I
would like to express my gratitude to all my CIS col-
laborators who made this work possible. I acknowl-
edge the following organizations for funding the
research discussed here: the McDonald Institute for
Archaeological Research, the Natural Environmental
Research Council, the Wenner-Gren Foundation, the
British Academy and the Leakey Foundation. I am
grateful to the University of Cambridge and the British
Academy for providing travel expenses to enable me
to attend the Havemeyer Workshop.
1Ahypothetical adjustment factor has been applied to com-
pensate for the probable under-representation of immature
animals (for details see Levine, 1983). To obtain the average
adjusted frequency of teeth for each age class from birth to
the age of five years, the frequency of teeth in each age class
(from 0 to 5 years) is multiplied by 1/0.23 +0.17(age). ‘Age’
refers to average age; for example, 0.5 is used for 0–1 years.
20 M. A. Levine
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... Depuis sa domestication supposée dans les plaines eurasiennes (IV e -III e millénaires BC, culture Botaï ; Levine, 2005), le cheval 1 a eu un impact économique, social et politique non négligeable sur les sociétés humaines. Monté, attelé ou bâté, celui-ci offre à l'Homme une nouvelle perception de son environnement. ...
... L'âne a notamment été employé comme animal de transport (bât, attelage). la face mésiale ainsi que l'usure en biseau de la seconde prémolaire inférieure induite par le port du mors (Bendrey, 2007a;Brown & Anthony, 1998;Outram et al., 2009), les déformations de l'os nasal ou de la mandibule induites par le port d'un harnais (Bartosiewicz & Gál, 2013, p. 134;Taylor et al., 2015), les affections du squelette axial telles que la spondylose (Baron, 2018;Bartosiewicz & Bartosiewicz, 2002;Janeczek et al., 2014;Lignereux & Bouet, 2015) ou les fractures vertébrales (Levine, 2005) et les arthropathies (Bartosiewicz et al., 1997;Bartosiewicz & Bartosiewicz, 2002;Janeczek et al., 2017) (Dutour, 1992;Jurmain et al., 2012;Villotte & Knüsel, 2013). ...
... Cette altération peut être interprétée, à tort, comme une fracture du corps vertébral, certaines études archéozoologiques rapportant ce type de cas chez le cheval (e.g. Baron, 2018;Levine, 2005). Pour le cheval 1.5, cette altération relèverait davantage d'un évènement intervenu après le décès de l'animal. ...
Les changements enthésiques correspondent à des atteintes des zones d’insertion des tendons et ligaments sur l’os (ou enthèses). Si ces altérations sont fréquemment employées comme marqueurs osseux d’activité en anthropologie biologique, ces dernières font l’objet d’un intérêt récent pour explorer les interactions entre l’Homme et les équidés. Intégrer ces marqueurs aux recherches archéozoologiques contribuerait à l’apport de nouvelles connaissances sur ce sujet notamment au travers des activités auxquelles étaient dédiés ces animaux. Ce travail propose une nouvelle méthode de cotation s’intéressant à 23 enthèses du squelette appendiculaire des équidés. Cette dernière est employée sur un corpus de 61 spécimens modernes documentés. Leur étude permet de mettre en évidence qu’il est possible de distinguer (1) les individus employés dans le cadre d’activités humaines de ceux qui en sont exempts ainsi que (2) les différentes fonctions pour lesquelles certains d’entre eux étaient employés (monte, traction). Il est démontré que la pratique d’une activité n’est pas la seule étiologie à intervenir dans le développement de changements enthésiques. En effet, des paramètres tels que l’âge au décès, les proportions corporelles ou les conditions de vie sont à considérer. Cette démarche est ensuite appliquée sur les 21 chevaux découverts au cours des fouilles du quartier Saint-Brice de Tournai (Belgique), en périphérie de l’emplacement supposé de la tombe du roi Childéric 1er décédé en 481-482. Associée à une étude paléopathologique approfondie, les analyses des modifications enthésiques contribuent à dresser l’ostéobiographie de ces équidés et obtenir des indices quant à leurs conditions de vie. Les anomalies osseuses et dentaires relevées laissent penser que ces animaux étaient en bonne santé au moment de leur décès. Les changements enthésiques fournissent un argument supplémentaire en faveur de l’hypothèse selon laquelle ces chevaux étaient utilisés comme montures. Nos recherches démontrent ainsi le potentiel de l’emploi de ces atteintes lors de l’étude des restes osseux d’équidés mis au jour en contexte archéologique.
... Species such as cattle, horses, goats, reindeer, and pigs shift into feral states easily and survive without human interference (Lazo 1994;Naundrup and Svenning 2015). Genetics, use wear, population structure, osteometrics, stable isotopes, artifacts, and ethnographic evidence have all been brought to bear on the question of whether an animal is wild or domestic (Balasse et al. 2016;Levine 2005;Perry and Makarewicz 2019;Zeder 2012). Previous research on degrees of ferality have focused on the Eurasian origins of livestock and pastoralists (Chen et al. 2016;Taylor 2017;Vermeersch et al. 2021). ...
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In North America, the introduction of livestock as part of the Columbian Exchange had profound social and ecological consequences for cultural environments, yet the landscape impacts of these animals have been difficult to identify, particularly in the first decades of sustained contact. Between 1701 and 1775, at a Spanish colonial mission near what is today Nogales, Arizona, O'odham groups and Spanish missionaries generated land management practices that wove together the needs of domesticated animals and existing Indigenous farming practices. This study proposes a set of indicators to identify animal husbandry practices in both the archaeological and historical record. Faunal, isotopic, and historical analyses from Mission Los Santos Ángeles de Guevavi provide evidence that cattle ages were loosely monitored and that cattle were culled at an older age than optimal for meat and grease extractive strategies compared to other domesticated species at the site. These findings suggest a low investment strategy in cattle, which may have helped Indigenous groups continue aspects of precontact agricultural and gathering practices and preserve their communities in the colonial period. These findings provide further evidence of the depth of animal husbandry practices among Indigenous groups in the Southwest.
... 、东 欧的德瑞 夫 卡 (Deriivka) (Levine, 1990(Levine, , 2005 Anthony et al, 1991)、西亚的安纳托利亚(Anatolia) (Benecke, 2006;Arbuckle, 2012)、中亚的博泰(Botai) (Outram et al, 2009;Bendrey, 2011 ...
... To advance this research field, comparative studies with other domesticated animals, such as horses, are essential. Horses have had a close relationship with humans since they were first domesticated approximately 6000 years ago [13][14][15] . In accordance with this long history of horse-human interactions, recent studies have shown that horses can follow human pointing in object-choice tasks to find the location of hidden-food 3,4 . ...
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When interacting with humans, domesticated species may respond to communicative gestures, such as pointing. However, it is currently unknown, except for in dogs, if species comprehend the communicative nature of such cues. Here, we investigated whether horses could follow the pointing of a human informant by evaluating the credibility of the information about the food-hiding place provided by the pointing of two informants. Using an object-choice task, we manipulated the attentional state of the two informants during food-hiding events and differentiated their knowledge about the location of the hidden food. Furthermore, we investigated the horses’ visual attention levels towards human behaviour to evaluate the relationship between their motivation and their performance of the task. The result showed that horses that sustained high attention levels could evaluate the credibility of the information and followed the pointing of an informant who knew where food was hidden (Z = − 2.281, P = 0.002, n = 36). This suggests that horses are highly sensitive to the attentional state and pointing gestures of humans, and that they perceive pointing as a communicative cue. This study also indicates that the motivation for the task should be investigated to determine the socio-cognitive abilities of animals.
The llama (Lama glama) and the alpaca (Vicugna pacos) are important domesticated species, endemic to South America. South American camelids helped ensure the success of humans in the Andes, much like the horse in Europe. Two wild South American camelids, the guanaco and the vicuña have been proposed as the ancestors of these domestic forms. Some scientists have hypothesized that crossbreeding started after the Spanish conquest in the 1500's, since before this event, indigenous people are thought to have kept both domestic breeding lines separate. In an effort to avoid the confounding effects of crossbreeding, ancient DNA from pre-conquest South American camelids was analysed from sites in Bolivia and Ecuador. Our mitochondrial pre-conquest results for Cerro Narrío in Ecuador show that all ancient samples which do not naturally occur in this region and were likely domesticated camelids, had maternal guanaco ancestry. At the Bolivian site of Iwawi, near Lake Titicaca, matrilineal ancestry from both wild species contributed to the domestic forms. These results help disentangle the complex ancestry of the domestic South American camelids and inform future breeding strategies. Additionally confirm the occurrence of crossbreeding between camelids pre-Spanish conquest.
The uncertainties in the load and resistant parameters of structures generally lead to a design with failure probability. In reliability-based design optimization (RBDO), the probability of structural failure is defined as an optimization constraint to consider the effect of these uncertainties. The smart improvement and combination of optimization and reliability methods in RBDO is very important and sensitive, especially for complex engineering structures. In the present study, the line sampling method has been improved using the horse optimization algorithm (HOA) to deal with the mentioned issue. The motivation for using these two methods is their high accuracy and speed in solving complex problems. The solution used to achieve this goal is in a way that the random samples are generated along the important direction vector (α), and then HOA uses these points to find the position of the limit state function. Different problems including highly nonlinear, high dimensions, passive vehicle suspension system, and vehicle side impact are considered to evaluate the performance of the proposed method, and the answers are compared with that of the existing methods. Overall, the results indicate an increase in accuracy and speed of problem-solving by the present method.
Optimal power flow plays an important role in integrating wind power into electric power networks. Because of its complexities, standard formulae are insufficient for the present scenario. Therefore, the multi-objective optimal power flow problems for wind farm incorporated power systems have been explored in this paper. The objectives are to minimize the generation costs, pollutant emissions, power losses, and voltage deviations. This paper proposes the development of a multi-objective meta-heuristic horse herd optimization for solving multi-objective optimal power flow problems. For this, a decomposition concept is introduced to the proposed algorithm leading to decomposition based multi-objective horse herd optimization algorithm. The constraint handling techniques in the previous papers have been found to be inefficient for optimal power flow problems. Therefore, a novel constraint handling technique is proposed in this paper to effectively control the variables out of bounds. In order to validate the performance and suitability of the proposed algorithm, seven case studies are examined. The algorithm is tested on wind farm incorporated IEEE-30, IEEE-57, and IEEE-118 bus test systems to demonstrate the efficiency in solving multi-objective optimal power flow problem for various problem sizes. The experimental results are demonstrating the efficiency of the proposed algorithm in solving complex optimization problems of various scales with multiple objectives.
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The archaeological research carried out in caves and rockshelters provided fundamental information for our understanding of the past, especially for the periods and regions dominated by groups with a hunter-gatherer economy. In spite of its clear importance, information on the use of caves and rockshelters by anatomically modern humans has encountered the persistent problem of the representativeness of the occupations in this naturally confined locations. In this research, a cross-cultural survey of ethnographic foragers was carried out in order to understand in depth the relationship between the use of caves/rockshelters and the organization of human groups. The interrelationships between the use of these places and the environment, mobility, technology, subsistence and land use are here analyzed and compared. Ethnographic records show a great variety of uses for these kind of sites, much more than what is usually considered in literature. Likewise, it is concluded that residential use, frequently cited, only occurs at low latitudes. At high latitudes, the combination of resource distribution, mobility strategies and the existence of means of transport make residential occupation unlikely. The information obtained suggest the existence of differences in the representativeness of the archaeological record of caves in relation to the surrounding archaeological landscapes.
Conference Paper
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A vast impact concerning cancer research has been made by researchers analyzing the expression of thousands of genes at the same time and relating them to clinical phenotypes by DNA microarray technology. The large dimensions of gene expression microarray datasets, combined with a lack of samples and irrelevant or noisy genes, make classification tasks more difficult. The purpose of gene selection is to identify the most informative genes in order to enhance prediction results. The Horse Herd Optimization Algorithm (HOA) is a novel swarm intelligence algorithm for solving continuous optimization problems, which simulate the behavior of a herd of horses. This study introduces a binary version of the Horse Herd Optimization Algorithm (BHOA) for solving discrete problems in biological data. Moreover, this paper introduces a novel hybrid gene selection framework that combines BHOA and a minimum Redundancy Maximum Relevance (mRMR) method. mRMR is applied as a filter approach to reduce noisy and irrelevant genes as well as to reduce the high computational cost that swarm intelligence algorithms generally suffer. The proposed approach's performance was examined using four well-known datasets: DLBCL, Colon, SRBCT, and Leukemia. According to the experimental results, the hybrid approach performed better than all the other methods regarding both accuracy and the number of selected genes.
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Horses were domesticated for more than 5000 years and have been one of the most emblematic species living alongside humans. This long-shared history would suggest that horses are well known and well understood, but scientific data raise many concerns about the welfare state of most domestic horses suggesting that many aspects have been largely misunderstood. In the present review, we will examine some of the possible human factors that may explain the huge prevalence of welfare problems, despite horses being of special importance to humans. First of all, as horses are non-verbal, current management practices rely upon what one thinks is good for them, which opens the way to subjective interpretations and projections, based on one’s own subjective experience but probably still more on cultural/social norms and influences, traditions and beliefs. The lack of recognition, identification, or even the misinterpretation of signals are other potential reasons for welfare issues. Lastly, the over-exposure to animals with expressions of compromised welfare may lead to lower sensitivity of owners/professionals. That is why we lastly suggest that instead of simply providing information on what to do, we should promote validated visible indicators that leave less room for personal interpretation.
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The domestication of the horse was revolutionary in its consequences – as much so as the spread of agriculture, trade, warfare, metalwork and the other more usual subjects addressed by archaeologists studying post-Neolithic human development. For not only did it directly cause important changes in peoples' relationships to the world around them by the mobility it conferred, but also it was deeply implicated in all those other developments. In spite of that, in the past 15 years very little has been done to extend our knowledge of the subject. This study, if anything, shows that we probably know even less about the earliest domestication of the horse than we thought
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The question of the origin and evolution of horse husbandry is one of the most interesting and most disputed problems in history. This paper uses palaeopathology to explore this problem. Samples of equid thoracic vertebrae from 4 populations - free living Exmoor ponies, Early Iron Age Scytho-Siberian horses, Medieval Turkic horses and Eneolithic horses -are compared. Preliminary results suggest that the abnormalities of free-living horse caudal thoracic vertebrae differ from those of riding horses and most especially from those of horses ridden with pad saddles.
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This case study describes a Romano-British horse skeleton from Icklingham, Suffolk. Although the skeleton was articulated and was found near a human skeleton, the two burials appear to be unrelated. The horse was not accompanied by artifacts and appears to have been disposed of after a violent, traumatic injury to its back, which probably indirectly caused its death.
The culture-historical development of Neolithic and Bronze Age communities under Eurasian steppe conditions is indissolubly linked with the establishment and development of early forms of productive economy, and displays a number of distinguishing features, which are the product of both natural and historical factors. Within the USSR, the steppe extends from the mouth of the Danube to the upper reaches of the Ob and the Altai mountains (Milkov 1977). To the north, the steppes naturally grade in to the forest zone to form a belt of transitional foreststeppe landscape. To the south, the steppe is bounded by the coast of the Black Sea, the foothills of the Caucasus and beginning in the Lower Volga region the semi-deserts and, further south, deserts of Soviet Central Asia.