SMITHSONIAN MISCELLANEOUS COLLECTIONS
VOLUME
85,NUMBER
10HUMAN HAIR AND PRIMATE PATTERNING
(With Five Plates)
BY
GERRIT
S. MILLER, JR.Curator, Division ofMammals,U.S. XationalMuseum
(Publication 3130)
CITY
OF WASHINGTON
PUBLISHED BY
THE SMITHSONIAN
INSTITUTIONDECEMBER
19, 1931HUMAN HAIR AND PRIMATE PATTERNING
By GERRIT
S.MILLER,
JR.,curator, division ofmammals, u. s. national
museum (With
Five Plates)Few
problemshave
causedmore
perplexity to anthropologists, physicians,and
zoologists than those presentedby human
hair.Why
is it that only
some
relatively small areas of thehuman
skin are normally capable of bearing a hairgrowth
denseenough
to be inany way
comparable withthe fur of othermammals? Why
domen
have beardsand women
not?Why
are beards better developed insome
racesthan inothers?What
is the cause of baldness,and why
is thereno
certain cure for it?Why
does baldnesscommonly
occur ort thecrown and
rarelyon
the sides of thehead? Why do we
turn gray?Why
does grayness usuallyshow
itself firston
the temples or in the beard?Why
does themoustache
often remain dark after the beard has turnedgray? Why do we
have hairy eyebrows,and why, when
there is a difference in colorbetween
the hair of theeyebrows and
that of thehead, are theeyebrows
usually thedarker of thetwo
?Why
is the hair of the scalp often difTerent in qualityfrom
that of other parts of thebody? Why
are there severaltypes of hair—
kinky,curly
and
straight?To
all of these questions somany and
such unsatisfying answers have been suggested that itwould
be ahuge and
useless task to try to list them. Variableand
inconclusivethough
they are,most
of theanswers
possess one quality incommon,
namely, they have in theirbackground
the tacitassumption that all these peculiarities ofhuman
hair are things that arise
from
man's special constitutionand
itsreactionto the natural environment or tothe artificial conditions that
man
hasimposed upon
himself. It has, for instance, been urged that thegeneralbarenessof thehuman
skincomes from
thewidely preva- lent habit ofwearing
clothes; that baldnesscomes from
barbersand
tight-fitting hats; that
women
have less baldness thanmen
becausewomen have
for centuries taken better care of their scalps thanmen
have; that graying hair is the result of a lessening bodily energy supposed to
go
with increasing civilization or "domestication;" that the axillaryand
pubic tufts of hairwere
once useful for babies toSmithsonian MiscellaneousCollections, Vol. 85,No. 10
2
SMITHSONIAN MISCELLANEOUS COLLECTIONS
VOL. 85cling to; that
eyebrows
exist for the purpose of keeping sweatfrom
runningdown
into the eyes; thatmen
are bearded to protect their throatsfrom
cold weather; thatwomen
are beardless because they look better that way. All ofwhich
gives evidence of ingenuity if of nothing else.But
not one of the explanations that I have been able to find in print has taken into consideration the zoological possibility thatmany
features of the
human
hair systemmay
be generalized primatetraits instead of specifically
human
developments.By
this Imean
the possibility that they
may
be characteristics that are forced onman
because they arecommon
property of the Primates, the animalgroup
towhich man
pertains. Theirexplanation, in thatevent,would
have to bemade
less in terms ofhuman
activitiesand
requirements than in terms of the great heritage of characteristics thatman
shares withall his primate relatives.Each
one of these creatures has modi- fied his portion of this heritage in such away
as tomake
it hisown
or, in
more
technical language, each one of the800-odd
kinds of living apes,monkeys, and
lemurs has developed " specific " charactersby which
it can be distinguishedfrom
all the others while remainingnone
the less a primateamong
primates. That,,man
should have done thesame
thingwould
be farfrom
strange.This paper is a brief
summary
of a studyon which
I have beenengaged
for several years with the result that I havebecome
con- vinced that the chief peculiarities ofhuman
hair are bestand most
simply explained as specialexamples
of primate "patterning."WHAT
ISMEANT BY "PATTERNING"
Patterning is familiar to every systematic zoologist because it is
seen in every
group
of animals. It consists in thearrangement
of (a) contrasted colored areas on the surface of the body, or (b) contrasted longand
short outgrowthsfrom
the surface of the body, or (c) combinations of colorsand
outgrowths, in such amanner
that the resulting patterns of color orform
are sufficient to distinguish one related speciesfrom
another.Familiar
examples
of patterning are furnished by the colormark-
ings of butterflies, or of theAmerican wood
warl)lers, by the minute surface sculptureon
the shells ofsome
mollusks,and by
the spiny outgrowths on the backand head
of the different species of iguanaand
horned-toad.Among mammals,
strikinginstancesareprovidedby
cats
and
squirrelswiththeirdiversestripes, spots,mottlings,and
plain colors,and by
African antelopes with their stripesand
spots as well as theirmaned
necks, fringed throatsand
briskets,and
tufted tails.NO. 10
HUMAN' HAIR AND PRIMATK PATTKRNING MILLER
3The making
of patterns appears to be a process quite distinctfrom
that by
which
a general harmonizing of animals with their natural surroundings has been effected. Nearly allied, pallid, desert species, for instance,may
be distinguishedfrom
each other by details of indi vidual pattern as obvious as those that serve tomark
richly colored species living inhumid
forests. General types of colorand
surfacemay
have their relations to the surroundings inwhich
animals pass their existence; but the special patterns of the species thatconform
to
any
one type cannot beshown
to have such relations. Itmay
be plausibly argued that the blotchedand
spotted color schemes of arboreal warblersand
the streaked color schemes of grass-living finches have something to do with the unlike surroundings in which warblersand
finches pass their lives.But
thisargument would
not apply to the dift'erences between the patterns of Blackburnian and black-throated green warblers nesting togetheramong
thesame
ever- greens, nor to those between savannahand
grasshopper sparrows living in onemeadow.
Still lesswould
it be possible to explain, ongrounds
of special needs,why
species of horned-toad differfrom
each other in thenumber and form
of the spiny outgrowths on the head, orwhy
one species ofgnu
has a fringe on the brisketand
another hasnot. Patterning, therefore, seemsto be something physio- logically inherent in animals rather than something that the environ-ment
hasimposed upon
theuLPATTERNING
INPRIMATES
Though
patterning occurs in all groups ofmammals —
even inrhinoceros, hippopotamus, elephant,
and
cetacean—
it isamong
the primates that the tendency attains its greatest development. In no othergroup
does itmake
such full use of its chief materials, namely, the color of the skin, the color of the hair,and
the contrasts that can be obtainedfrom
dift'erences in qualityand
length of hair.No
l)etter
example
of this process could be given than the one furnished by the headmarkings
ofmonkeys grouped
on Plate i.The
animals there represented are nearly related species that live underessentiallyuniform
surroundingsinthegreatAfrican forestbelt.No two
ofthem
havethesame arrangement
of darkand
lightareas on the head; three liave conspicuous white stripes over the eye; onehas a black stripe in thesame
place;infive thecheeksare white, while inthree they are not white; one (fig. 2) isbearded, while sevenare not; one (fig. 4) hasa moustachelikemark
of white in the skin of the upper lip; another has a boldly contrasted spot of fine white hairs on the nose.Other
patterns in priiuatescome from
lengthening, shortening,and
\aryingthe direction of
growth
of the hair on different.parts of the crown, alsofrom
varying the lengthand
quality of the hairon
the chest, shoulders, tail,and
legs,and from making
contrasts, oftenmore
striking than the one seen in the white-lipped
guenon shown on
Plate I, in the color of different portions of the skin itself. All of theseelements of colorand
hairgrowth
arecombined and
recombined in avariety thatseems
to be without end.On no
part of the primateform
is patterning so conspicuously developed ason
the head,where
strikinglymarked
color designs of both hairand
skin are profusely exhibited,and where
tufts, beards, moustaches, whiskers,and
crestsarebrought intovaried contrast with areas of short hairand
bare skin.PATTERNING ON THE HUMAN HEAD
In conformity with this universal primate trait
human
patterningshows
itselfmore
conspicuouslyon
thehead
thanon
thebody
orlimbs.The human head
pattern is not exactly duplicatedby any
other primate, but all the elements that enter into it can be easilyfound
innonhuman members
of the order.The
usualheadpattern of theyoung
adultCaucasian isshown
inPlate 2, Figures iand
2. Characteristics that both sexeshave
incommon
are the completely haired cranium, the bald forehead, nose,and upper median
part of the cheeks,and
thepresence of anarrow
transverse hairy stripon
the forehead over eacheye.The
female'spatterndiffersfrom
themale'sinanextension of the bare areadownward
over theentire lower part of the faceand
sidewaysto the ears.In
most
primates the foreheadand
face, except the region im- mediately bordering the eyes, noseand
mouth, are thickly haired.The
first step in the process of baring the forehead isshown by
one of the Celebean macaques,Magus
hecki (pi. 2, fig. 3).Other
stepshave
been takenby some
of theSouth American monkeys
; whilean
essentiallyhuman
forehead can befound
in the orang (pi. 2, figs.4, 6).
The
bare or nearly bare lower part of the face seen in the females of allhuman
races,and
in the males of those races inwhich
the beard is slightly developed, is presagedby
the verycommon
occurrence
among
other primates of a short-haired, nearly bare areaaround
themouth (shown by
allof themonkeys
representedonpi. i).Extensions of this bare area
on
the cheeksmay
be seen in the great apes. It is carried farther insome
of theSouth American monkeys,
culminating, apparently, in the '* cotton head,"Oedipomidas
oedipus(pi. 2, fig. 5),
which
has reacheda stage slightlymore advanced
than that of thehuman
female.NO. 10
HUMAX HAIR AND PRIMATE PATTERNING MILLER
5Though
a bare or nearly bare condition of themouth
area is the usual conditionamong nonhuman
primates, itis notuniversal.Beards
like those of the male Caucasian or Australian occur in the orang
(pi. 2, fig. 6), in the bearded African
guenon shown
at the top of Plate I,and
in aSouth American monkey
{Pithecia chiropotes) ofwhich
I have not been able to obtain a photograph.Moustaches
are notcommon among
primates.Even
that of the fuU-beardcd orangis poorly developed.
But
theSouth American Mysiax hnpemtor
(pi. 2, fig. 7) goes far to
make up
for this deficiency.While
neithermoustache
nor beard is peculiar toman
the strong development of bothtogetherappears to beahuman
specialty.Nothing
exactly like thehuman eyebrows
isknown
in other pri- mates, but thebrow
region is onewhere
patterns aremade
in great profusion.Sometimes
thesebrow
patterns take theform
of light ordark stripes (asshown
inpi. iand
inpi. 4, figs. 10and
13) ;some-
times theyaremade by
lines of hair differingin qualityand
directionfrom
that of thehead
(pi. 2, fig. 8), thusshowing
a near approach tothe conditionfound
inman. Human eyebrow
hair,asiswellknown,
often differs in colorfrom
the hair of the crown. In such cases (pi. 4, figs. II, 12) it is usually darker than thecrown
hair, after themanner
of the gray-cheekedmangabey
(pi. 2, fig. 8) or theHimalayan
langur (pi. 4, fig. 10) ; rarely if ever is it conspicuously lighter, after that of the white-browed gibbon (pi. 4, fig. 13).This
normal human
pattern does not always remain constant throughout life.Changes
oftwo
kinds usually take place;and
the courses of both kinds tend to follow lines that can be traced through thegroup
of primates at large.TURNING BALD
With
arrival at full maturity a considerable percentage ofhuman
males
undergo
a modification of their hair pattern that serves to differentiatethem
still furtherfrom
the females.The
forehead line begins to rise, either uniformly along its entire extent (pi. 3, fig. i), or,more commonly, by
pushing back ablunt reentrantwedge on
each side (pi. 3, fig. 4). Frequently a bare spot begins toform
at thesame
timeon
the top of thecrown
(pi. 3, fig. 6),and
the hair of the entiremedian
part of thecrown becomes
sparse.These
changesmay
continue until the bald forehead area has been carried back over the
dome
of the head, leaving a well-haired border extendingaround
the sidesand
across thenape
(pi. 3, fig. 8).This series of maturity changes inthe hair coveringof the
human
male head
has been the subject of endless speculation.By
afew
writers ithas been recognized to be, likethebeard, asecondary sexual character/ but, so far as I
am
aware,no
one has hithertoshown
thatit follows the lines laid
down by
the patternings of other primates.The uniform
raising of the forehead line can befound
as a specific characterinthebaldchimpanzee
;itisexactly paralleledby
thepattern of shortand
long hairs on the head of oneSouth American monkey.
Pithecia
monachns
(pi. 3, fig. 2),and by
the colorpattern of another,Cebus
hypoleucus (pi. 3, fig. 3).The
development of thetwo
bluntwedges
results in apatternmuch
like the one present in the Celebean black ape, Cynopithecus niger (pi. 3, fig. 5).The
bald spoton
top of thecrown
is an occasional character of the toque macaque,Macaca
pileata (pi. 3, fig. 7).The
completely developedhuman
bald area (pi. 3, fig. 8) is perfectly outlined in the
South American monkey known
as Cacajao ruhicimdus (pi. 3, figs. 9and
10).The
long darkhairatthesideand
back of theheadof this animaloccupies the area that remains haired innormal human
baldness, while the light hair onthemedian
area corresponding with thehuman
bald spot is so shortand
sparse that it does not conceal the skin of the scalp in the living animal(two
have recently beenon
exhibition in the National Zoological Park). Finally it isto be noticed that thehuman
bald area follows the outline of the dark cap of theWest
African gorilla (pi. 5, fig. 5) as well as that of a color pattern not infre- quently seen in blondmen.
This pattern, (which appears to occur inwomen
also, but is obscuredby
long hair) isproduced by
an obviously paler tint of the hair thatgrows on
the bald-spot area.It is visible as a faint but accurate picture of the color pattern
made
by a bare scalp contrasted with dark side hair.At
theHarvard com- mencement
exercises of 1930 Isaw
it on the heads of seven of theyoung men
awaiting the conferring of their degrees.TURNING GRAY
Another
change in thehuman
hair that begins at or slightly after theattainmentof full maturity is seen inthe familiar process of turn- inggray; thismay
lead in theend
to a stagewhen
all the pigmented hairs of the entirebody
have been replacedby
colorless ones.This loss of color, like baldness, has given rise to conjecture with- out end.
And,
as in the case of baldness, its near relation to primate patterning seems to have passed unnoticed. Nevertheless, it can be*Tlie examination of many liundreds of photographs makes it appear prob- able that the males of races with strong beards tend to show the highest per- centage of baldness, thus differentiatingthemselvesmost fully fromthe females.
NO. lO
HUMAN HAIR AND PRIMATK PATTERNrXG MILLER
7shown
tohave thesame
tendencyto follow themain
lines of primate pattern making.When
gray hairs begin to replace the pigmented ones theydo
not appearuniformly all over the body. "A
vigorousman
just beginning toshow
atouch of gray on thetemples" isan often-heard phrase that unconsciously recognizesthis fact.When
beardswere common among
us everyoneknew how
usual itwas
forthem
to turn gray before the scalp.As
they increase innumbers
the gray hairs tend toform
patterns.These
are sometimes nothingmore
than faint sketches or suggestions.Often, however, they develop into striking color contrasts.
The
faint
and
fugitivehuman
patterns are not always easy to correlate with the patterns of other primates, but the definite ones rarely pre- sentany
such difificulty.Eight of these well defined
human
color patterns with their]~)rimatehomologues
areshown on
Plates 4and
5.The
firstand
second (pi. 4. figs, iand
3). consisting of a white beardcontrasted with a dark crown, are frequently seen. In the firstthe
mouth
area is white. In the second it is dark.Both
occur inmany
species ofmonkey, two
of which, the African Erythrocchus pyrrJionotusand
CcrcopitliccusUwcstl, areshown
in Figures 2 and4.The
identity is so obvious that it requires nocomment.
The
third pattern (pi. 4. fig. 5). consisting of a white chin beard sharply contrasted with dark whiskersand
head, is lesscommon.
Sometimes
the w^hite involves the moustache. It is then exactly thesame
as the white area in the Africanmonkey
CcrcopitJiccus hrazzac (pi. 4, fig. 6). I have seen several examples of thishuman
pattern with white moustache, I)Ut have not yet secured a photograph.The
fourth pattern (pi. 4, figs. 7, 8, 9) is merely a darkmark
on the cheekmargin
of agray beardaccompanying
a gray or bald liead.Insignificant
though
thismarking may
seem, it is surprisinglycom- mon. On
April 21, 1930, I visitedtheJewish pushcart marketdistrict inNew York
City, one of thefew
convenient placeswhere many
full beards can
now
be seen, to look for this mark. I found it in no less than 47 out of 55men
with gray or white beards.The same
dark line at the edge of the longer hair on the cheeks isfound
inmany
of themonkeys
that have a partly baremedian
facial area.An
example
isshown
in Plate 4, Figure 10, theHimalayan
langur (Pygafhrix scliisfacca). Itmay
be easily observed inimmature
Japanese macaques, animals that are often exhibited in zoological gardens.The
grayhuman
temple spot (pi. 5, fig. i) is acommon
feature of primate color patterning. It is particularly well developed in the geladababoon
(pi. 5, fig. 2).As
they increase in size the temple spots often extendbackward
along the sides of thehead
until they cover the entire area that re-mains
haired innormal
baldness.The
pattern thusformed —
dark capcontrasted with grizzled sides
and
back ofhead
(pi. 5, figs. 3, 4)—
is a
common
oneamong non-human
primates. It is particularly well developed in theWest
African gorilla (pi. 5, fig. 5.The
specimen representedby
thisphotograph
isan unmounted
skin with thehead
not filled out to natural form). Occasionally this patternmay
be seen reversed.The
grizzlingisthenconfinedtotheareaof thenormal
bald spot, while the hairs at the sidesand back
of thehead
remain dark.When
thishappens
the colorscheme
of the cacajaomonkey
(pi. 3, fig. 10) is reproduced.
White
locks situatedon
or near the forehead line (pi. 5, figs. 6, 7) arenotuncommon,
buton
other parts of thehead
theyarerare.They may
bepresentwithoutother signs of thegrayingprocess (asinfig. 6) or theymay
appear as a step in thatprocess (as in fig. 7). In either event theyare usually confinedtosome
part ofan
areawhere
pattern- ing occurs innonhuman
primates (pi. 4, fig. 6, pi. 5, fig. 8^).PATTERNING ON OTHER PARTS OF THE HUMAN BODY The
process of turning grayusuallybeginson thehead and
extends graduallydownward
over the body.As
it advances it often passes through astage, particularly well represented in Figure9
of Plate 5, inwhich
the gray area ends abruptlyat the middleof the chest, leav- ing the hair of thearms and
lowerpart of thebody
dark.The
general lines of apatternfound
inan
African colobusmonkey,
Colobuspoly- comos,and
inanAsiaticmacaque,Macaca
albibarbata (pi. 5, fig. 10), are thenclosely followed.Turning
to other parts of thehuman body we
find that thesame
correspondence with widelydistributedprimatetendenciesholds good.The
pubic region is an area of pattern formation in widely sepa- ratednonhuman
primates.Young
chimpanzeeshave
a white pubic patch contrasted with the black surrounding hair. It disappearsby becoming
black before theanimals reach full maturity.Some
species of gibbon haveno
pubicmark
whatever. Others display a black spot*The spidermonkey representedinfig. 8 of pi.5 has aband ofwhite extend- ing along the entire frontal border of the true head-hair. The forehead-hair
is also white, but it differs from the head-hair in quality and in direction of growth. Before photographingthis skin Idarkened the forehead-hair with ink.
NO. 10
HUMAN HAIR AND PRIMATE PATTERNING MILLER 9
that Stands out against its pale surroundings. Still another gibbon hasthe hair of thisregion so greatly lengthened that, in adult males,
it
may form
atassel reaching almost to the knees.A South American
monkey {Oreonax
hendcei) has a long yellow hair tuft in themale and two
shorter tufts in the female. In both sexes the tufts are rendered very conspicuousby
contrast withthe darkbellyand
thighs.By
specializing the hair of this regionman
has, therefore, merely followed one tendency of his tribe.The
last conspicuous hair-pattern feature ofman
is the tuft in thearm
pit. This, perhaps,comes
the nearest of all the patterns to beingan
exclusivelyhuman
trait; I have not yet seen an exactly similar development inany
other primate. But,on
gently blowing the hair of the axillary region of a freshly dead Africanmonkey,
Cercopithe- cus aethiops, I oncefound
that the hairsgrowing
in the deepest part of the pit tended to separate themselvesfrom
the surrounding furby
a slightdifference in qualityand
in the direction of growth.More
recently I have been able to see, in several adult chimpanzees,* that these animals have a definitely specialized axillary tuft confined to the region of greatest glandular activity.
To
produce thehuman
condition it
would
merely benecessary to suppress the long surround- ing hair.SOME OTHER FEATURES OF HUMAN PATTERNING A few
other points abouthuman
patterning require brief mention.(a)
The
general bareness of thehuman
body.Why
thehuman body
lacks a protecting general coat of fur is a question that has been often askedand
variously answered.A
finalexplanation seems to be as remote
now
as ever; but it is possible to recognize the fact thathuman
bareness is only an exaggeration of a tendency that isfound
in other primates,"and
that it isno more
essentially mysterious than the bare face of one tropical
American monkey
(pi. 2, fig. 5)when compared
with the fully haired face of another (pi, 2, fig. 7). In neither instance can it beshown
that a special need of the species is servedby
the bare skin; but in both it is evident that the tendencyfound
throughout the primategroup
toform
patternsby
contrasting long-haired areaswithshort-haired areas has beencarriedtoan extreme.^At the Yale University Anthropoid Experiment Station, Orange Park, Fla.,
anopportunityforwhichI havetothankProfessorYerkes andDr.Tinklepaugh.
^On
this subject see Schultz,Human
Biology,vol. 3, pp. 303-321, September, 1931,and Sci. Monthly,vol. 33, pp. 392-393, November, 1931.The
general distribution of longerand
shorter hair on thebody
of gorillas rather closely coincides with thehuman
scheme.By
continu- ing the process along the linesmarked
out in this great ape a stagewould
eventually be reached inwhich
thebody would become
bare while thearms and
legs retained traces of their original coat.(b)
The
differentfacepattern ofmen and women.
The
sexual hair pattern on thehuman
face is another subject of age-long speculation.No
one has ever been able toshow
that itspresencehasaidedman'scareer as aspecies. Equallyimpossible
would
itbeto
show
thattheanalogous sexual patternsin other primateshave given these speciesany
advantage over their relatives that lack them.But
it seemsclear that in this respectman
has developed in thesame
generalway
as the white-cheeked gibbon of Siam, the orangs ofBorneo and
Sumatra, the black howlermonkey
ofSouth
America,and
themacaco lemur
of Madagascar, all ofwhich
have sexes that differfrom
each other in appearance.That
is to say,man and
these other primates have followed a tendency thatmay
crop outanywhere
in the
group
of animals towhich
they all belong.(c) Racial dift'erences in hair pattern
and
in general color of the hair.It is well
known
that not all races ofman
are exactly alike in hair pattern.Some
havebetter developed eyebrows, beards, pubicpatches, or axillary tufts than others;some
appear to be not as subject as others to graynessand
baldness. Racial tendenciestoward
darker or lighter colored hair are also wellknown. These
racial characteristics have never been satisfactorily explained on the basis of the special needs of different peoples.On
the other hand, as examples of the slight differencesthat areeverywhere found among
races of primates nearly related to each other they are readily understood.The
differencesbetween
thetwo
races of orang, for instance, are of thisnature.The United
States NationalMuseum
contains6
malesand
6 females of theSumatran
orang,6
malesand
lo females of theBornean
race, all adult or nearly adult.These two
seriesshow
thesame
kind of differences that areshown by
races ofmen.
In thefirst place, the beards of the males aremuch
better developed than those of the females.Then, when
thebeardsof theSumatrans
arecompared
withthose of theBorneans
theyareat onceseentobe larger, somuch
so that an adult male
from
either island can usually be recognized at onceby
this feature alone. Finally there is a general difference in the color of the hair onbody and
head, this beingmore tawny
in theSumatran
race,more mahogany brown
in the Bornean.NO. lO
HUMAN HAIR AND PRIMATE PATTERN
INCJMILLER
IIThese two
races of orangs inhabit separate parts of one cHniatic zone, exactly as Caucasiansand MongoHans
inhabit opposite ends of another. Therefore the differences in hairgrowth
can be nomore
attributedto the influence ofunHke
naturalsurroundingsinthe second instance than in the first. But it seems clear that thetwo
races of orangand
thetwo
races ofmen
are both in early stages of species differentiation,and
thatthemanner
of their differentiatingis onethat iscommon
tothewhole
primate group.(d) Total graying.
Often, though not invariably, the process of turning gray culmi- natesin a stage of complete whiteness.
But
evenwhen
ahuman
being has turned gray over the entirebody
or even has lost all hair color he hasdone
nothing that is essentiallynew
or peculiar for a primate.Light gray or nearly white species of primates have arisen in both Asia
and South
America.These
animals are not albinistic nor in anyway
individually abnormal. Their near relatives, living in thesame
regions, are richlycolored;and
there is nothing to indicate that either light or dark hasany
advantage over the other. General grayingand
whitening inman
seems likely to be nothingmore
than another ex-ample
ofhuman
submission to a rule thatsome
other primates have followed. Therefore the strong tendency present in the " white race "of
man
for the hair to lose its color at an early agemay
be part of a racial process of depigmentation that has already almost whitened the skinand
thatmay
be destined, in the future, to I)ring aboutpermanent
whitening of the hair as well.CONCLUSION
For
the present I wish to avoid detailed discussion of the published attempts to explain those peculiarities ofhuman
hair that have just been passedinreview.Most
of the authorswho
have considered the subjecthavedone
sofrom
the view-point that these peculiaritiesmust
have originatedfrom
conditions (pathological or cultural) or needs (physiological or esthetic) that pertain exclusively toman. That
this view-point iswrong
seems to be sufficiently indicatedby
the evidence hereselectedfrom
the largemass
that Ihave assembled. This evidence points to the probability thatman
has these characteristics because, as a primate, he cannot avoid theuLThey
arecommon
property of the greatgroup
ofmammals
towhich
hepertains,and
neither he norany
othermember
of thisgroup
can wholly escapefrom
the tenden- ciesimposed on
all ofthem by
their primate heritage.With
regard tono nonhuman
primate can it beshown
that the possession ofany
12
SMITHSONIAN MISCELLANEOUS COLLECTIONS
VOL. 85special assortment of these characteristics
makes
a species better,more
efficient, ormore
at ease inthe world than one that has another assortment.So
also withman.
The
similarities that I haveshown
to existbetween some
hair characteristicsofman and
those of particularmonkeys and
apesmust
not be supposed to indicateany
special relationshipbetween man and
these other primates.When
superficial features of this kind arecommon
to awhole group
they will often appear in almost identicalform
intwo
animalswhose
relationship isshown by
their anatomical structure to be remote.EXPLANATION OF PLATES
All figures greatly reduced, not to scale
Plate i
Color patterns on the heads of eight species of African guenon (Cercopithe- cus).
From
Elliot, after Pocock.Plate2
The
human
head-hair pattern and its characteristics as they occur in other primates.Figs, i, 2.
Young
adult Caucasian.Fig. 3. Partly bare forehead ofa Celebean macaque {Magus hecki).
Fig. 4. Bare forehead of an orang.
Fig. 5. Bare face of a "cotton head" {Oedipomidas oedipus).
Fig. 6. Beard ofan orang.
Fig. 7. Moustache ofa marmoset (Mystax imperator) Figs. 8, 8a. Eyebrows of amangaby (Cercocebusalbigena).
Plate3
Types of human baldnessand the corresponding conditions in other primates.
Fig. I. Raised
human
foreheadline.Fig. 2.
A
South American monkey (Pithecia mojtachus) with hair pattern corresponding with the raised human forehead line.Fig. 3.
A
South American monkeywith color pattern corresponding with the raised human forehead line.Fig. 4. The two reentrant forehead wedges in man.
Fig. 5. The two reentrant forehead wedges in the Celebean crested macaque (Cynopithecusniger).
Fig. 6. Bald spot at middleof crown
—
human.Fig. 7. Bald spot at middleof crown
—
toque macaque (Macaca pileata).Fig. 8. Complete, normal, human bald crown area.
Figs. 9, 10. Nearly bald crown area in a South American monkey {Cacajao rubicundns)
NO. 10
HUMAN HAIR AND PRIMATE PATTERNING MILLER
I3Plate4
(a)
Human
color patterns formed during the process of turning gray and thecorresponding patterns in other primates.Fig. I. White face contrasted with dark head in man.
Fig. 2. White face contrasted with dark head in an African monkey (Erytlt- rocebuspyrrhonotus)
.
Fig. 3. White face contrasted with dark mouth area and dark crown in man.
Fig. 4. White face contrasted with dark mouth area and dark crown in an African monkey (Cercojyithecus I'hocsti).
Fig. 5. White chin and lower lip contrasted with dark face and Iiead in man.
Fig. 6. White chin and mouth area contrasted with dark face and head in an African monkey {Cercopithectisbraszae).
Figs. 7, 8, 9. Darkarea atedge of lightcheekhair in man.
Fig. 10. Dark area at edge of light cheek hair in an Asiatic monkey (Pyga- thrixschistacea)
.
(b) Eyebrow patterns, human and simian.
Figs. 10, 12. Dark eyebrows contrasted with light head hair.
Fig. II. Dark eyebrows contrasted with hair that has turn<;d white.
Fig. 13. White eyebrows contrasted witli black head (white-browed gibbon, Hylobates hoolok).
Plate 5
Human
color patterns formedduring theprocessof turning gray and thecor- respondingpatterns in other primates (continued).Fig. I. The human gray temple area.
Fig. 2. The gray temple area in the gelada baboon (Theropithecus gelada).
Figs. 3, 4. The human gray temple area extendedaround the head.
Fig. 5. Color pattern on thehead of the East Africangorilla.
Figs. 6, 7. White locks on the human forehead line.
Fig. 8. Whitestripealongtheforeheadline ina South American spider
monkey
(Atclcs hybridus).
Fig. 9. Gray area extendingdownwardfrom head tomiddleof chest in man.
Fig. 10. Gray area extending downward from head to middle of chest in an Asiaticmonkey (Macaca albibarbata)
.
SMITHSONIAN MISCELLANEOUS COLLECTIONS VOL. 85, NO. 10, PL. 1
"",..
:f
PatteniiiiL! on the lirads oi ei.ylit species ni Alrifaii monkey,
(Kiir cxiilaii.-iliiiii si-c ]). u.]
^W
QO.
Human
face ])atte'nis cmnparrd with tin.- analogous patterns ol' five Isinds of nonlinman primates.(I''iu- c.xiilaiuitioii sec- p. 12.)
SMITHSONIAN MISCELLANEOUS COLLECTIONS VOL. 85, NO. 10, PL. 3
T.
3
hiinnii haldiR-s.^ pattmis tnmiiarfd with the analni^ciu.s iiatlirii> ui li\e kinds of
111inlniiuan primates.
(I'"(ir c.xiilanatiiiii sec p. u.
)
Figs. i-io.
—
lluniaii .!;rayiK->s i)attcTns cimiparrd willi the aiialn.^DUN pattcni.s of four kindsof nonlnnnan primates.Figs. 10-13.
—
Eyebrow patterns. Inniian and simian.(For cxiilanatidii sfo |). i,;.')
SMITHSONIAN MISCELLANEOUS COLLECTIONS VOL. 85, NO. 10, PL.5
Human
,m"a\nL'Ns ]iattrnis rDmiiarnl with .'lualonous ])atKTii.s nl' I'nur kinds u niiiiluunan |iriniaU's.{l-nr (x|i|.inaticiii sec p. i.i.)