Psychology of Prejudice and Discrimination 3rd Edition Ebook PDF
Psychology of Prejudice and Discrimination 3rd Edition Ebook PDF
Psychology of Prejudice and Discrimination 3rd Edition Ebook PDF
Preface xxvi
Acknowledgments xxix
Glossary 579
References 592
Name Index 681
Subject Index 706
vii
This Page is Intentionally Left Blank
D E TA I L E D C O N T E N T S
Preface xxvi
Acknowledgments xxix
ix
x DETAILED CONTENTS
Self-Report Measures 51
Assessing Stereotypes 51
Assessing Prejudice 52
Assessing Behavior 52
Unobtrusive Measures 53
Physiological Measures 54
Research Strategies 62
Correlational Studies 62
Survey Research 63
Experiments 67
Laboratory Experiments 70
Field Experiments 70
DETAILED CONTENTS xi
Content Analysis 73
Meta-Analysis 75
Drawing Conclusions 76
Verifying Results 77
Summary 80
Suggested Readings 82
Key Terms 83
Why We Categorize 87
Types of Categorization 91
Subtypes 92
Prototypicality 93
Situational Influences 96
Level of Prejudice 97
Consequences of Categorization 98
Ingroup Overexclusion 99
Summary 121
Prototypicality 131
Prejudice 134
Comprehension 136
Self-Enhancement 137
Individuals 153
Summary 163
Summary 207
Individualism 213
Egalitarianism 215
Religion 222
Conclusions 227
Authoritarianism 228
Emotions 239
Empathy 252
xvi DETAILED CONTENTS
Summary 253
Categorization 289
Summary 296
Self-Categorization 305
Summary 337
Microaggressions 347
DETAILED CONTENTS xix
Disinhibitors 358
Hiring 363
Normalization 381
Summary 384
Course 394
Concealability 395
Origin 395
Danger 396
Tokenism 397
Summary 433
Summary 476
Ability 499
Appearance 510
Height 513
Weight 516
Summary 521
Self-Regulation 531
Cooperation 539
Personalization 549
The periproct (Fig. 228, 4) is covered with small plates and bears a
few pedicellariae. The peristome (Fig. 229) is covered by flexible
skin with abundant pedicellariae; it terminates in a thick lip
surrounding the mouth, from which the tips of five white teeth are just
seen projecting. There are ten short tube-feet projecting from the
peristome—one pair in each radius—and each tube-foot terminates
in an oval disc and is capable of little extension, and each has
around its base a little plate. The presence of these tube-feet shows
that in Echinus the peristome extends outwards beyond the water-
vascular ring, whereas in Asteroidea it is contained entirely within the
ring. In the primitive Cidaridae (Fig. 235) the whole peristome down
to the lip surrounding the mouth is covered with a series of
ambulacral and interambulacral plates similar to those forming the
corona, though smaller and not immovably united, and the series of
tube-feet is continued on to it. It is thus evident that the peristome is
merely part of the corona, which has become movable so as to
permit of the extension of the teeth. In Echinus the peristome is
continued in each interradius into two branched outgrowths called
gills, the relation of which to the respiratory function will be described
later. These gills (Fig. 229, 2) are situated in indentations of the edge
of the corona called "gill-clefts" (Fig. 230, g).
The term ambulacral plate, applied to the plate pierced by the pores
for the tube-feet, conveys a misleading comparison with the
ambulacral plate of an Asteroid. In Echinoids the ambulacral groove
has become converted into a canal called the "epineural canal," and
the ambulacral plates form the floor, not the roof, of this canal; they
may perhaps correspond with the adambulacral plates of the
Starfish, which one may imagine to have become continually
approximated as the groove became narrower until they met.
Fig. 231.—Dissection of Echinus esculentus. × 1. The animal has been opened
by a circumferential cut separating a small piece of the skeleton at the
aboral end, which is turned outwards exposing the viscera on its inner
surface. The other viscera are seen through the hole thus made. amp,
Ampullae of the tube-feet; aur, auricle; b.v, so-called "dorsal blood-vessel";
comp, "compasses" of Aristotle's lantern, often termed "radii" by English
authors; comp.elv, elevator muscles of the compasses; comp.ret, retractor
muscles of the compasses; eph, epiphyses of the jaws in Aristotle's lantern;
gon, gonad; g.rach, genital rachis; int, intestine; oe, oesophagus; prot,
protractor of Aristotle's lantern; rect, rectum; ret, retractor of Aristotle's
lantern; siph, siphon; st, stomach; stone.c, stone-canal.
The buccal tube-feet (Fig. 229, 4) are much shorter than the rest,
and are provided with oval discs which are highly sensory. These
feet are not used for seizing, but for tasting food; when a piece of
food is placed near them they are thrown into the most violent
agitation.
Fig. 232.—Diagrammatic transverse section of the radius of an Echinoid.
amb.oss, Ambulacral ossicle; amp, ampulla of the tube-foot; ep, epineural
canal; musc, muscles attaching spine to its boss; nerv, nervous ring in base
of spine; n.r, radial nerve-cord; oss, ossicle in sucker of tube-foot; ped,
tridactyle pedicellaria; perih, radial perihaemal canal; pod, tube-foot; wv.r,
radial water-vascular canal.
The nervous system has the same form as in an Asteroid, viz. that
of a ring surrounding the mouth and giving off radial nerve-cords
(Fig. 232, n.r), one of which accompanies each water-vascular canal
to the terminal tentacle, where it forms a nervous cushion in which
pigmented cells are embedded.
When a piece of glass rod or other light object is laid on the spines of
a Sea-urchin, it naturally, by its weight, presses asunder the spines
and stretches their muscles on one side, thus lowering the tone. If
now the skin be stimulated at any point the piece of rod will be rolled
by the spines towards the point of stimulation. This is caused by the
fact that the muscles of the spines holding the rod are made more
receptive by being stretched, and therefore they contract more than
do the others in response to the stimulation, and so the rod is rolled
onwards on to the next spines, which then act in the same manner.
This passage of stimulus is entirely independent of direct nervous
connexion between the bases of the spines, for it will traverse at
right angles a crack going clean through the shell; it is merely the
result of the mechanical weight of the object and of the juxtaposition
of the spines.
If the stimulation be too violent the first spines affected diverge wildly
and strike their neighbours with vehemence, so arousing into activity
the block musculature of these. This causes them to stand rigidly up,
and so the path of the stimulus is barred.
Now the escape movements of the animal under strong stimulation
which Romanes[480] alludes to are just an example of this handing
on of stimulation from spine to spine, not by nervous connexion but
by mechanical touch only; the object in this case is the substratum
on which the animal lies, which is, so to speak, rolled towards the
point of stimulation, or putting it otherwise, the animal is rolled away
from it. Righting when upset is another example of the same
phenomenon; the aboral spines are stretched by the weight of the
animal, and the animal acts as if it were stimulated in the region of
the periproct. When a Sea-urchin is in its normal position and is
stimulated in the periproct (as for instance by a strong light), it would,
according to this rule, tend to move downwards, which is of course
impossible; but as the stimulus never affects all sides quite alike the
result is that the Urchin rotates, turning itself ever away from the
point of strongest stimulation. In the case of Strongylocentrotus
lividus when living on limestone, as on the west coast of Ireland, this
results in the animal excavating for itself holes in the rock, where it is
safe from the action of the breakers.[481]
The central nervous system is, however, the system which controls
the movements of the tube-feet. As we have seen, extensions of the
radial nerves run to the tip of each podium. Tube-feet are chiefly
used in ordinary progression; when this is quickened the spines
come into play exclusively. The extent to which these two organs of
locomotion are used varies from genus to genus. Thus
Centrostephanus uses its spines a good deal, Echinus and
Strongylocentrotus very little. The last-named genus sometimes
walks on its tube-feet entirely without touching the ground with its
spines.
Besides the tips of the tube-feet the Urchin possesses another kind
of sense-organ, the sphaeridia (Fig. 233). These are minute glassy
spheres of calcareous matter attached by connective tissue to
equally minute bosses on the plates of the ambulacra, generally near
the middle line. They are in fact diminutive spines, and like the latter
are covered with a thick layer of ectoderm, beneath which is a
particularly well-developed cushion of nerve-fibrils. Only the layer of
muscles which connects a normal spine with its boss is wanting.
Although definite experimental proof is lacking, the whole structure of
the sphaeridia shows that they belong to the category of "balancing
organs." As the animal sways from side to side climbing over uneven
ground, the heavier head of the sphaeridia will incline more to one
side or to another, and thus exercise a strain on different parts of the
sheath, and in this way the animal learns its position with regard to
the vertical.
In the outer wall of this space are developed the calcareous rods
forming Aristotle's lantern. These are first: five teeth (Fig. 234, 11),
chisel-shaped ossicles of peculiarly hard and close-set calcareous
matter, the upper ends (1) pushing out projections of the upper wall
of the lantern-coelom. These projections are the growing points of
the teeth, whose lower ends pierce the ectoderm and project into the
lower end of the oesophagus. Each tooth is firmly fixed by a pair of
ossicles inclined towards one another like the limbs of a V and
meeting below. Each ossicle is called an "alveolus," and taken
together they form a "jaw." Their upper ends are connected by a pair
of ossicles called "epiphyses" (13). These two epiphyses meet in an
arch above. The jaws and their contained teeth are situated
interradially. Intervening between successive alveoli are radial pieces
called "rotulae," which extend directly inwards towards the
oesophagus. Above the rotulae are pieces termed "radii" or
"compasses" (2), which are not firmly attached to the other pieces
but lie loosely in the flexible roof of the lantern-coelom.
The genital rachis springs from the upper end of the stolon, and as in
Asteroids, it lies in the outer wall of a space called the "aboral sinus"
(Fig. 234, 20) intervening between it and the test. In adult specimens
it seems to degenerate. The genital organs are situated at the ends
of five interradial branches of the rachis (Fig. 231, gon). Each is an
immense tree-like structure consisting of branching tubes, which are
lined by the sexual cells. So enormous do they become in the
breeding season that they form an article of food among fishermen.
The term esculentus is derived from this circumstance. Other
species are regularly sold for food as Frutta di Mare (Fruit of the
Sea) at Naples, and as "sea eggs" in the West Indian Islands. One
female Echinus esculentus will produce 20,000,000 eggs in a
season.
The so-called blood system is more distinctly developed in
Echinoidea than in Asteroidea and Ophiuroidea. There is an oral ring
of lymphoid tissue surrounding the oesophagus below the water-
vascular ring. From this are given off two strands, the so-called
"dorsal" (Fig. 231, b.v), and "ventral" vessels (Fig. 234, 16), which
run along the two opposite sides of the stomach or first coil of the
alimentary canal. The position of these strands suggests that like the
lacteals of the human intestine they are channels along which the
products of digestion exude from the stomach. The dorsal strand is
situated on the same side as the genital stolon, and from it branches
are given off which ramify on the surface of the stolon, on account of
which this organ, as in Asteroidea, was at one time regarded as a
"heart," but the distinction of the stolon from the strands is easily
made out. An aboral ring enclosing the genital rachis lies embedded
in the septum dividing the aboral sinus (Fig. 234, 20) from the
general coelom.
Classification of Echinoidea.
The Echinoidea are sharply divided into three main orders, which
differ from each other profoundly in their habits and structure. These
are: (1) The Endocyclica or Regular Urchins, of which the species
just described may be taken as the type. (2) The Clypeastroidea or
Cake-urchins, which are of extremely flattened form, and in which
the periproct is shifted from the apical pole so that it is no longer
surrounded by the genital plates, while some of the tube-feet of the
dorsal surface are flattened so as to serve as gills. (3) The
Spatangoidea or Heart-urchins, in which the outline is oval: the
periproct is shifted, as in the Cake-urchins, and the dorsal tube-feet
are similarly modified; but the Heart-urchins have totally lost
Aristotle's lantern, whilst the Cake-urchins have retained it. This
strongly-marked cleavage of the group was primarily due, as in all
such cases, to the adoption of different habits by different members
of the same group. Were we to term the three orders Rock-urchins,
Sand-urchins, and Burrowing-urchins, it would not be entirely true,
for secondary invasions of the other's territory on the part of each
order have undoubtedly taken place; but still the statement would
remain roughly true, and would give a fair idea of the differences in
habitat which have led to the differentiation of the group.