FIGURES OF SPEECH:
POSSIBLE NEURO-PHYSIOLOGICAL BASES?
Renato
COCCHI MD, a neurologist and a medical psychologist
To prof. Faustino Savoldi
and prof. Francesco Zerbi, of
with my unchanged gratefulness
Summary
Figures of speech are the most used style's tools in speaking and in
writing. Their use is common to peoples living in countries without any
knowledge of our rhetoric.
Many figures of speech can act by adding a non-rational conscious force
of persuading to the argumentation; nearly all stimulate the curiosity of the
target; some modify prosody or rhythm of speaking.
A new type of analysis showed that 90 figures of speech spread into four
mechanisms related to the neural network functioning of the brain. These
mechanisms categorize perceptive stimuli according to identity by similarity,
identity by space contiguity, post hoc ergo propter hoc (or cause and effect's
relationship by temporal contiguity), and opposition.
The different levels (grammatical, syntactic, semantic, phonetic,
rhythmic, attentional) where figures of speech apply themselves and the
mechanism or mechanisms involved give peculiar features to each of them.
Figures of speech are not exclusive of verbal language, but they can be
found in other perceptive fields too, as painting or advertising in the visual
field,
Key words: Figures of speech; neural basis; perception; brain
mechanisms similarity; space contiguity; time contiguity; opposition.
Figures of speech (FS) are the most used style's tools in speaking and in
writing. When carefully observed, they show some features, not always in
common. Many of them can act by adding a non-rational conscious force of
persuading to the argumentation; nearly all stimulate the curiosity of the
target; some modify the prosody or the rhythm.
The
first feature gives help to form a judgement, to reach a decision, so making
known itself as involved into cognitive mechanisms. The second and the third
ones lead to keep up the attention of the listeners or the readers, and that
represents the way to assure a better communication.
Many
people using FS seem completely unaware of many problems these put
forward.
One can sum these problems up as it follows:
- Do
FS have any common grounds?
- How
FS work?
- Why
FS work?
- Why
FS work even out of verbal language?
- Why
FS work even out of verbal language?
- Are
there any FS in languages other than Indo-Europeaî ones?
About
14 years ago, I published a paper on identity by similarity and identity by
contiguity as perceptive mechanisms used for acquiring verbal language in
infants (Cocchi, 1982). I wrote on their use to explain some figures of speech.
Following
that, now I would try to give few answers to these questions, the first one
looking at the possibility that FS have some common basic elements.
A proposed new classification
of figures of speech
Attempts
to classify FS have a long history, since Quintilian, but all these had their
reference to language itself. From first aware users to the current debate,
people agree that rhetoric is the refinement of a natural skill, but this skill
seems mainly confined in verbal language. (Vickers, 1988).
I
believe that only reaching a different founding basis we could explain the use
of many FS in visual communication, mainly in advertising now. However nothing
we can say on the power of persuading many FS possess. So, I think verbal
language as the preferred field where FS bloomed, but we have to search
somewhere else, in more primary mechanisms related to the neural network
functioning.
Materials and method
According
to that FS have feelings, as their target, the first question to answer was
indeed if FS have some common features, so reducing their great variety.
The
way I used for this goal was to check all FS by dividing them into four fields
of belonging. They are similarity, space contiguity, post hoc, ergo propter hoc
(ie. for that because after that) or temporal contiguity, opposition.To this I
added specification by trying to identify the level or the levels (emotional,
phonologic, semantic, grammatical, etc.) where that FS is applying. To the
remaining questions, I shall answer by inference. I found the figures of speech
I investigated in handbooks of rhetoric (Mar- chese, 1978; Vickers, 1988) which
list them in alphabetical order.
Results
I
could collect and analyse 90 FS. Table 1 shows the results I obtained from the
analysis. In that table simil. means similarity, contig. stays for space contiguity,
post hoc is a short for Post hoc, ergo propter hoc, alias time contiguity and
eventially oppos. for opposition. Other keys: X = leading mechanism; x =
secondary mechanism; (?) supposed mechanism; phon.= phonetic; syn= syntactic;
gram.= gramatical; sem.= semantic, attn.= attentional; sens.= sensorial; emot.=
emotional.
Table
1: Analysis of FS, in alphabetical order, and level or levels of working. (From Accumulation to Apostrophe).
|
Figure |
similar |
contig |
post hoc |
opposit |
level1 |
level2 |
|
Accumulation |
x |
X |
(?) |
x |
syn |
sem/emot |
|
Adnomination |
X |
|
x |
|
gram. |
sem. |
|
Adynaton |
|
|
x |
X |
sem. |
emot. |
|
Allegory |
X |
|
|
|
sem. |
|
|
Alliteration |
X |
|
|
|
phon. |
sem. |
|
Allusion |
x |
X |
|
|
sem. |
attn. |
|
Amplification |
x |
X |
|
|
sem. |
attn. |
|
Anaclasis |
X |
|
x |
|
sem. |
phon. |
|
Anadiplosis |
X |
x |
|
|
phon. |
attn. |
|
Anaphore |
X |
x |
|
|
phon. |
attn. |
|
Anastrophe |
|
x |
|
X |
syn. |
rhyth. |
|
Anticlimax |
|
x |
X |
|
sem. |
rhyth. |
|
Antimetabolis |
x |
x |
x |
X |
syn./phon |
sem. |
|
Antimetathesis |
x |
x |
x |
X |
syn./phon |
sem. |
|
Antiphrasis |
|
|
|
X |
sem. |
|
|
Anthypophore |
|
x |
X |
(?) |
attn. |
syn. |
|
Antithesis |
|
(?) |
x |
X |
syn. |
sem. |
|
Antonomasis |
X |
x |
(?) |
|
Sem. |
|
|
Apostrophe |
X |
|
|
|
emot./sem |
|
Table
1: Analysis of FS, (Following: From Asyndeton to Metaphor ).
|
Figure |
similar |
contig |
post hoc |
opposit |
level1. |
level2. |
|
Asyndeton |
|
X |
x |
|
syn |
sem |
|
Assonance |
X |
|
|
|
phon. |
sem. |
|
Auxesis |
|
X |
X |
|
gram./sem. |
rhyth. |
|
Brachilogy |
|
X |
|
|
gram/rhyth |
attn. |
|
Calembour |
X |
x |
|
|
phon./sem. |
|
|
Captatio benevol. |
X |
|
x |
|
emot. |
|
|
Catacresis |
X |
|
|
|
sem. |
|
|
Cataphore |
|
|
X |
|
syn./sem. |
attn. |
|
Chiasm |
x |
X |
x |
x |
syn. |
sem. |
|
Climax |
|
(?) |
X |
|
sem./emot. |
|
|
Comparison |
X |
x |
|
|
sem. |
syn. |
|
Concatenatio |
x |
X |
x |
|
syn. |
sem. |
|
Concessio |
|
|
x |
X |
emot. |
sem. |
|
Correctio |
x |
x |
X |
|
sem. |
emot. |
|
Deprecatio |
X |
x |
x |
|
emot. |
|
|
Diaphore |
X |
|
x |
|
phon./sem. |
|
|
Dicolon |
X |
x |
|
|
syn. |
attn. |
|
Dilemma |
|
(?) |
x |
X |
sem./emot. |
syn. |
|
Dubitatio |
X |
|
|
x |
attn. |
sem. |
|
Ecphoresis |
X |
x |
x |
|
emot. |
attn. |
|
Ellipsis |
|
|
x |
X |
syn. |
attn. |
|
Enallages |
|
|
X |
(?) |
gram. |
sem. |
|
Emphasis |
X |
x |
(?) |
|
emot./sem. |
syn. |
|
Enumeration |
|
X |
x |
|
syn. |
sem. |
|
Epanadiplosis |
X |
|
(?) |
|
syn. |
sem. |
|
Epanalepsis |
X |
x |
x |
|
sem. |
syn. |
|
Epanortosis |
X |
x |
|
|
sem./emot. |
attn. |
|
Epiphoneme |
X |
x |
x |
|
sem. |
syn. |
|
Epiphore |
X |
|
X |
|
syn. |
sem. |
|
Epiphrasis |
|
|
X |
|
syn. |
sem. |
|
Epizeusis |
X |
X |
|
|
syn. |
|
|
Euphemism |
X |
|
|
|
emot. |
|
|
Etimol. figure |
X |
|
|
|
sem. |
|
|
Geminatio |
X |
|
|
|
sem./emot. |
attn. |
|
Homoteleute |
X |
x |
x |
|
gram./sem. |
attn. |
|
Hypallages |
|
x |
x |
X |
sem. |
syn. |
|
Hyperbatos |
|
X |
|
x |
rhyth. |
syn. |
|
Hyperbole |
X |
|
x |
|
emot. |
sem. |
|
Hysteron-proteron |
|
X |
|
|
attn. |
syn. |
|
Invective |
|
X |
|
|
emot. |
syn. |
|
Inversio |
|
|
|
X |
attn./sem. |
|
|
Irony |
|
|
x |
X |
sem. |
emot. |
|
Isocolon |
x |
|
X |
|
syn. |
sem. |
|
Iunctura |
|
X |
x |
|
sem. |
syn. |
|
Litotes |
|
|
|
X |
emot. |
sem. |
|
Meiosis |
X |
|
(?) |
|
sem. |
|
|
Metalepsis |
X |
x |
x |
|
sem. |
|
|
Metaphor |
X |
x |
x |
|
sem. |
|
Table 1: Analysis of FS, (Following: From
Metonymy to Zeugma ).
|
Figure |
similar |
contig |
post hoc |
oppos |
level1 |
level2 |
|
Metonimy |
|
X |
|
|
sem |
|
|
Onomatopoeia |
X |
|
|
|
emot. |
phon. |
|
Oxymoron |
|
x |
(?) |
X |
attn. |
sem. |
|
Paradox |
|
|
|
X |
sem. |
attn. |
|
Paralipsis |
|
(?) |
x |
X |
attn. |
sem. |
|
Paronomasia |
X |
X |
|
|
morph. |
sem. |
|
Percontatio |
|
X |
x |
|
emot. |
|
|
Personification |
X |
x |
|
|
emot. |
|
|
Polysyndeton |
|
X |
x |
|
rhyth. |
attn. |
|
Preterition |
|
|
X |
x |
emot. |
sem. |
|
Prolexis |
X |
|
x |
|
emot. |
syn. |
|
Periphrasis |
X |
X |
|
|
sem. |
|
|
Pun |
X |
(?) |
x |
|
phon./sem |
|
|
Regression |
x |
|
X |
|
syn./attn. |
sem. |
|
Reticence |
|
x |
X |
|
emot./attn |
|
|
Sarcasm |
|
|
x |
X |
emot. |
|
|
Simile |
X |
|
|
|
sem. |
syn. |
|
Syllexis |
|
x |
X |
|
syn. |
sem. |
|
Synecdoche |
x |
X |
|
|
sem. |
|
|
Synesthesy |
X |
|
|
|
sens. |
sem. |
|
Zeugma |
x |
x |
X |
|
gram. |
sem. |
As one can see in Table 1, every FS found
its place into one of the four proposed categories, as for its first field of
belonging. I did not always check over the second or the following fields of
belonging with certainty. It is to note the complexity of this division, which
parallels the different classification of the same FS linguistics did.
|
Table 2: Distribution of FS according
to four brain mechanisms. ------------------------------------------------------------------------------------------- |
|||||||
|
-------------------------------------------------------------------------------------------- |
|||||||
|
Primary mechanisms |
43 |
|
19 |
|
17 |
|
16 |
|
|
|
|
|
|
|
|
|
|
Secondary mechanis. |
11 |
|
29 |
|
31 |
|
6 |
|
|
|
|
|
|
|
|
|
|
Supposed secondary |
0 |
|
6 |
|
6 |
|
7 |
Table 2 shows similirity and space
contiguity as first brain mechanisms involved.
Discussion
As for these categories (i.e. similarity,
space contiguity, post hoc ergo propter hoc, and opposition), I will refer
again what I wrote in previous papers (Cocchi, 1993; 1996) with some new
details.
There is quite a long history about
similarity and contiguity of perceptions as conditions the brain not only
processes but has also some awareness of them. In other term the brain proves
to be aware of how some neural effects of external or internal stimuli spread
out through brain areas. Pribram 1976 stated as rules of reversible
transformation:
"3. Nerve impulses arriving
simultaneously at neighboring locations are spatially superposed, i.e.,
neighborhood interactions of an addictive (or subtractive) nature take place.
4. When two sources simultaneously evoke
a state in the slow potential microstructure, correlation between them takes
place and the correlations becomes decoded into nerve impulses."
These two rules give support the
detection of similarity and spatial contiguity.
So, by pointing out ways of neural
network functioning he gave a neural basis to what Jacobson and Halle 1956 and
Jacobson 1963 have argued.
These last authors wrote about a
mechanism's disruption of making similarities by partial identity (metaphors)
or of that making similarities by spatial contiguity ( metonymies [perhaps also,
or better, synecdoches]).
By myself, I referred to these two
mechanisms to explain why English infants say "comed" instead of
"came" when they are learning to talk. The same happens when the
Italian infants learn speaking and say "aprito, coprito" instead of
"aperto, coperto" (Cocchi, 1982).
Human brain works by making partial
identities or identities by similarities (metaphors) and identities by space
contiguity (Metonymies or synecdoches) out of the verbal language too.
Alcoholics did wrong answers by mostly
using space contiguity, as it came about for demented (Pola, Zerbi &
Cocchi, 1988), college students ( Cocchi, 1993). The same did alcoholics
scoring less than 20, or scoring between 20 and 25 at RCM (Cocchi, 1993; 1996).
Similarity (or, better, identity by
similarity) runs as quarter in a sample of alcoholics scoring 21-25 at RCM
(Cocchi, 1996). This way of making mistakes was only as third in the previous
sample of alcoholics (Cocchi, 1993).
In men low-spatial-frequency selective
transient mechanisms dominated the perceptual process which underlie the
similarity judgments (Petersik, 1978).
Newborn babies aged 7 hours to 11 days 15
hours can perceive a similarity between a stimulus when moving and when
stationary. These findings suggest a degree of visual organization that is not
usually attributed to the newborn (Slater et al., 1985).
Neurophysiological experiments using
microelectrodes revealed that brain detection of similarity, on its lowest
level, involves neuronal units which answer selectively only to an attribute of
a stimulating event (Hebb, 1949; Pribram 1971; Olton and Samuelson, 1976). This
means that, if a stimulus' feature modifies itself, at this low perceptive
level the cell previously excited becomes silent, and the adjacent cell starts
firing. The same have been verified in the temporal visual cortex of the
monkey, where neurons responding to identity of faces are not the same which
respond to face expressions (Husselmo, Rolls and Baylis, 1989).
From that, brain seems perceiving an
elementary identity (identity of a distinctive feature) when the stimulus made
by it excites always the same cell or group of cells (Cocchi, 1982).
It can happen so 1. When two external
stimuli have a feature that induces firing of the same cells in the same time;
2. When an external stimulus owns the same feature seen in past in another
stimulus now recalled (comparison between an external and an internal
stimulus); 3. When the comparison of two recalled stimuli leads to the actual awareness
that a common feature was exactly the same (Cocchi, 1982).
Experiments were made in an artificial
neural network using adaptive algorithms derived from observations of cortical
neurons during associative learning. This network acquired concurrently two
distinct representations in response to presentation of stimuli. One resembled
to associative conditioning, defined in terms of its sensitivity to forward
pairing vs. simultaneous or backward pairing. The other reflected contiguous
pairing of stimuli (Berner and Woody, 1991). However space contiguity
need be carefully differentiated from
temporal contiguity, and could have its base on the so-called ephaptic
transmission of electric potentials between adjacent neurons.
The Post hoc, ergo propter hoc, besides
leading to a fallacy in logic, offers the ground where classical conditioning
stands. In the simplest cases also, it permits to learn a cause and effect
relationship based on temporal contiguity and contingency. This fact has
paramount importance in all animals because helps in the defence of themselves
and of their own species. Choice of nutrients, identification of danger, choice
of sexual partner and breeding of progeny need to make continuous cause and
effect relationships.
The nervous systems of a broad variety of
animals have evolved the ability to recognize predictive relationships between
events if these occur repeatedly in a temporarily contiguous manner. Contiguity
detection in Aplysia Californica owns these features. (Abrams and Kandel, 1988)
In Aplysia such an existing mechanism
normally works and the dually regulated adenylate cyclase might underlie the
temporal requirements for effective classical conditioning (Yovell, Kandel,
Dudai and Abrams, 1987; Abrams, Karl and Kandel, 1991)
Temporal contiguity detection is
surprisingly constrained across species and learning paradigms. This constraint
suggests that the neuronal mechanisms for contiguity detection may have been
conserved through phylogeny and may be limited in number (Ambrams and Kandel,
1988).
Finally opposition answers at RCM in
alcoholics take the second place soon after space contiguity (Cocchi 1966).
This fact parallels what I found both in college students and in the previous
sample of alcoholics (Cocchi 1993; Cocchi 1993).
The way opposition presents itself can
vary from true semantic to counterpart (or mirror), shape or colour opposition.
Doing RCM the object can choose opposition wrong answers only by shape or
colour opposition.
We discussed this brain mechanism when we
presented the first case of "mirror speaking" after brain surgery
(Cocchi et al., 1986). As we referred there after a literature survey,
opposition can also arise in a state of brain toxicity and alcohol is a
well-known poison for the brain. We can remember here what happens in some
neuropathological conditions.
When subjects have suffered from a
cerebral insult, often an ictus, but also as the result of an accidental trauma
or neurosurgery, mirror actions can appear. We can see mirror writing and/or
reading (Critchley 1928; Paradowski and Ginzberg, 1971; Streifler and Hofman,
1976, Fisher, Liberman and Shankweiler, 1978; Heilman, Howell, Valenstein and
Rothi, 1980; Tankle and Heilman, 1982; Feinberg and Jones, 1985 ) or even
mirror speaking ( Cocchi et al., 1986). Mirror behaviours are opposites, at
least space opposites.
There is an explanation supported also
through animal research (Orton, 1928; Noble, 1968; Bradshaw, Nettleton and
Patterson, 1973). Perceptive stimuli, usually visual, produce both an engram and
its opposite in the two half-brains in the same time. Normally the brain
suppresses the opposite, which has its place in the non-dominant hemisphere.
Under particular conditions this suppressing mechanism becomes inhibited, and
so the opposite shows itself as a mirror image. Not only writing, reading and
language can take on this mirror-like behaviour, but the handling of objects
can become reversed too (Feinberg & Jones, 1985).
These last researchers suggest that
lift-right orientation be not a unitary characteristic. They maintain it can
have a link to differential activation of the cerebral hemispheres, when
carrying out motor or other types of tasks.
It could be curious that 3-4 months'
infants could discriminate differences in orientation (even among obliques).
But they tended to view mirror images, especially lateral mirror image, as equivalent stimuli (Bernstein, Gross
and Wolf, 1978). Is the suppression mechanism of the opposite engram not yet
working at that age?
On the other hand, the mastering of the
co-presence of opposites was judged a feature of higher intellectual level
(Rothenberg 1973; 1982).
The presence of mirror writing or mirror
speaking witnesses double engrams also for internal stimuli. Opposition seems
involved in temporary, stable or stabilized prevalence of non dominant
half-brain in dextrals, a condition perhaps more frequent than what one can
imagine (Cocchi, 1994). I reported the first case where opposition concerns
emotional thinking in a "schizo-affective" woman (Cocchi, 1996).
Often in a day, emotional thoughts of that woman were the full opposites of
what she felt. She appeared unable to control these intrusive and emotionally
negative thoughts. The explanation suggested refers to disruption of the
suppressing mechanism of the opposite engram, and to stabilized opposite
half-brain dominance for emotional thinking, dealing with the compulsory
emerging of bad oughts.
Conclusion
Now I think I can answer to the questions
I forwarded at the beginning of this paper.
1. Figures of speech have a common ground
to be identified in mechanisms of neural network functioning. They allow to
perceive identities by similarity and by space contiguity, cause and effect's
relationships by temporal contiguity, and opposition by the opposite engram.
2. Figures of speech work by giving to
the verbal language the opportunity of exploiting these four mechanisms at
various levels where language can apply itself.
3. Figures of speech work because they
are a key for a waiting lock (simile). They help to persuade by making
identities (also emotional identities) or cause and effect's relationships, and
attract attention by pointing up oppositions.
4. There are many examples of what we
know as figures of speech, in different field. As for the visual field, allegory
in painting has a long history (eg. Tiepolo for Venice, Appiani for Napoleon).
Recently I have seen a pure visual oxymoron (The country into the town) in an
advertising campaign made by a leading Italian pasta producer. Being these four
mechanisms not solely related to verbal language, but common to all brain
structures, other perceptive fields can use them.
5. I owe Wickers the notice that peoples
living in countries without any knowledge of our rhetoric used figures of
speech. Among them we can count China, India, Persia, Arabia, Maori, Tikopia,
Bali, and Africa (see Wichers, 1988, for references). Although FS seem the
fruit of the so-called Western Countries, they bloom anywhere because they not
depend on a specific verbal language, but only on common CNS mechanisms.
Eventually I believe that these links
between rhetoric and CNS will open many research opportunities, from graphic
art to the language of mentally retarded.
References
Abrams T.W., Kandel
E.R.: Is contiguity detection in classical conditioning a system or a cellular
property? Learning in Aplysia suggests a possible molecular site. Trends
Neurosci. 1988, 11: 128-135.
Abrams T.W., Karl K.A.,
Kandel E.R.: Biochemical studies of stimulus convergence during classical
conditioning in Aplysia: Dual regulation of adenylate cyclase by
Ca2+/calmodulin and transmitter. J. Neurosci. 1991, 11: 2655-2665.
Berner J., Woody C.D.:
Local adaptations of two naturally occurring neuronal conductances gK + (A) and
gK + (Ca), allow for associative conditioning and contiguity judgments in
artificial neural networks. Biol. Cybern. 1991, 66: 79-86.
Bornstein M.H., Groos
C.G., Wolf J.Z.: Perceptual similarity of mirror images in infancy. Cognition
1978, 6: 89-116.
Bradshaw J.L., Nettleton
N.C., Patterson K.: Identification of mirror-reversed and non-reversed profiles
in same and opposite visual fields. J. Exp. Psychol. 1973, 99: 42-48.
Cocchi R.: Meccanismi
"logici" nella acquisizione del linguaggio verbale: Una ipotesi esplicativa
neurofisiologica degli ipercorrettismi. Riv. Neurobiol. 1982, 28: 162-190.
Cocchi R.: Analisi delle
risposte errate, date alle PM47 di Raven, Rev. 1962, Forma I, da un campione di
studenti universitari. Riv. Ital. Disturbo Intellet. 1993, 6: 83-90.
Cocchi R.: Alcolisti con
punteggio < 20 alle Matrici Colorate di Raven:Analisi degli errori. Riv.
Ital. Disturbo Intellet. 1993, 6: 269-275.
Cocchi R.: Alcoholics
scoring 21-25 at Raven's Coloured Matrices: The analysis of wrong answers. It.
J. Intellect. Impair. 1996, 9: 181-187.
Cocchi R.: Defective
hemispheric dominance and cognitive behaviour: Speculative considerations. It.
J. Intellect. Impair. 1994, 7: 19-27.
Cocchi R.: Intrusive
opposite emotional thinking in a chronic "schizo-affective" woman. A stabilized
inverse half-brain dominance of a specific function? It. J. Intellect. Impair.
1996, 9: 162-168.
Cocchi R., Pola A.,
Sellerini M., Tosca P., Zerbi F.: Mirror speaking after neurosurgery. Case
history. Acta Neurol. Belg. 1986, 86: 224-232.
Critchley M.: Mirror
writing. Kegan, London 1927.
Feinberg T., Jones G.:
Object reversal after parietal lobe infarction - A case report. Cortex 1985:
21: 261-271.
Fischer F.W., Liberman
I.Y., Shankweiler D.: Reading reversal and developmantal dyslexia: A further
study. Cortex 1978, 14: 595-510.
Hasselmo M.E., Rolls
E.T., Baylis G.C.: The role of expression and identity in the face-selective
responses of neurons in the temporal visual cortex of the monkey. Behav. Brain
Res. 1989, 32: 203-218.
Hebb D.O.: The organisation
of behaviour. A neuropsychological theory, Wiley, New York, 1949.
Heilman K.M., Howell G.,
Valenstein E., Roth L.: Mirror-reading and writing in assiciation with
right-left spatial discrimination. J. Neurol. Neurosurg. Psychiat. 1980, 43:
774-780.
Jacobson R., Halle M.:
Fundamentals of Language. Mouton, Den Haag, 1956.
Jacobson R.: Essais de
linguistique generale. Editions de Minuit, Paris 1963.
Noble J.: Paradoxical
interocular transfer of mirror-image discriminations in the optic chiasm
sectioned monkeys. Brain Res. 1968, 10: 127-151.
Olton D.S., Samuelson
R.J.: Remembrance of places passed: Spatial memory in rats. J. Exp. Psychol.
1976, 2/no. 2, April. (Consulted text: Olton D.S.: La memoria spaziale. Le
Scienze 1977, 19: 86-101).
Orton S.T.: Specific
reading disability - Strephosymbolia. JAMA 1928, 90: 1095-1099.
Paradowski W., Ginsberg
M.: Mirror writing and hemiplegia. Percep. Mot. Skills 1971, 32: 617-618.
Petersik J.T.: Possible
role of transient and sustained visual mechanisms in the determination of
similarity judgments. Percept. Motor Skills 1978, 47: 683-698.
Pola A., Cocchi R.,
Zerbi F.: Progressive Matrices PM
Pribram K.H.: Languages
of the brain. Experimental paradoxes and principles in neuropsychology.
Prentice-Hall, Englewood Cliff, 1971
Rothenberg A.: Opposite
responding as a measure of creativity. Psychol. Rep.1973, 33: 15-18.
Rothenberg A.: Janusian thinking and Nobel Prize laureates. Am. J.
Psychiatry 1982, 139: 122-124.
Slater A., Morison V., Town C., Rose D.: Movement perception and
identity constancy in the new-born baby.
Streifler M. Hofman S.: Sinistral mirror writing and reading after brain
concussion in a bi-systemic (oriento-occidental) polyglot. Cortex 1976, 12:
356-364.
Tankle R., Heilman K.M.: Mirror reading in right- and left-handers. Brain
and Language 1982, 17: 124-132.
Yovell Y., Kandell E.R., Duday Y., Abrams T.W.: Biochemical correlates
of short-term sensitization in Aplysia: Temporal analysis of adenylate cyclase
stimulation in a perfused membrane preparation. Proc. Natl. Acad. Sci. USA
1987, 84: 9285-9289.
Printed on It. J. Intellect. Impair. 1997, 10: 35-42.
Author's address: dr Renato COCCHI, via Rabbino 3
42199 Reggio Emilia
(Italy)
renatococchi@libero.it