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Dyscalculia Disconnection Preprint
Dyscalculia Disconnection Preprint
Abstract
Developmental dyscalculia is distinguished from unspecific mathematical learning
difficulties. Common diagnostic procedures are critically discussed. With reference to
neuroscientific studies, the hypothesis is discussed that developmental dyscalculia is a
specific disconnection syndrome caused by impaired development of certain cerebral neural
pathways (a component of the superior longitudinal fasciculus), which impairs the
connection between an area important for numerical competence (the intraparietal sulcus)
and other brain areas.
Consistent with this neurophysiological model, a cognitive model is described in which
mental connections between purely geometric representations (dot patterns, number lines)
and other kinds of representations (language, symbols, situations in word problems) are
impaired. This is the first neurocognitive description of developmental dyscalculia. This
model not only explains typical symptoms but is also the starting point for a new diagnostic
approach that aims to better distinguish developmental dyscalculia from nonspecific
mathematical learning difficulties. Examples of corresponding diagnostic items are
presented.
1. Introduction
If difficulties with basic arithmetic persist after elementary school, this may lead to serious
problems in everyday life (dealing with money, especially cash, time planning, driver’s
license, etc.), in further education or when looking for a job. The use of calculators and
smartphones does not resolve such problems.
In a report by the Every Child a Chance Trust/KPMG (Gross J., Hudson C. and Price D. 2009),
the annual economic damage caused by poor numeracy skills in the UK (lack of skilled labor,
public social spending, private insolvency, etc.) was estimated at £2.4 billion, which is higher
than the economic damage caused by dyslexia.
Mathematical learning difficulties (MLD), which can be caused by various factors, need to be
distinguished from Developmental Dyscalculia (DD). The latter is probably a congenital
neurological developmental disorder. Individuals with dyscalculia are recommended
qualified individual tuition over a longer period (Haberstroh and Schulte-Körne 2019).
It is estimated that between 3% and 7% of the population is affected by DD (see Chapter 6).
In Austria this would be between 270,000 and 630,000 people. Although free tutoring
programs in small groups are available in some regions to provide general additional support
to pupils, individual tutoring by a qualified person with relevant experience currently costs
around 50 euros per hour, which is affordable only for people from socially privileged
backgrounds. In Austria alone, at least 200,000 people with DD from socially disadvantaged
backgrounds do not receive adequate support and suffer serious professional and economic
disadvantages as a result.
There is much less research on dyscalculia than on dyslexia, which means that current
diagnostic procedures are unreliable (see Chapter 5) and often lead to false positive
diagnoses. As a result, educators who identify comprehension problems, familial or other
difficulties as the real cause of mathematical learning difficulties in children with false-
positive diagnoses may get the impression that DD as a developmental disorder does not
exist. However, based on neuroscientific evidence, it is undisputed in the relevant scientific
literature that DD exists as a specific developmental disorder.
The difficulties in diagnosis lead to a vicious circle for purely quantitative empirical studies:
the unsatisfactory state of research means that cognitive explanatory models for dyscalculia
are not available. Without such models, standardized tests can only detect unspecific MLD,
but not DD. For new quantitative empirical studies, this means that the group of test
subjects will not only include people with DD, but also people who have been diagnosed as
false positives. If the composition of the test and control group does not correspond to the
object of the study (DD), the gain in knowledge will remain limited, thus completing the
vicious circle. New cognitive models, such as the one presented in this paper, or empirical
studies in which subjects are identified not only by means of standard test batteries but also
by qualitative assessment by people who have a lot of experience with DD, may show ways
out of this circle.
Books aimed at a wider audience include Butterworth (2019) and Emerson and Babtie (2013,
2014, 2015). Of particular note is the new book by Noël and Karagiannakis (2022), which is
based on Noël's hypotheses pointing in a similar direction as the present article.
7. Neuronal systems related to numbers (ANS, OTS) and the intraparietal sulcus (IPS)
The cardinality of a set is the number of its elements. Numerosity is the same as cardinality,
but without number abstraction, i.e. without number symbols or number words being
involved. For example, many non-human animals understand the numerosity of small sets,
they can judge which set has more or less elements (see Nieder 2019), but they do not
understand what the cardinality of a set is, because they are not familiar with the human
concept of number.
Caray (2001) and later Feigenson, Dehaene and Spelke (Feigenson 2004) distinguish two
innate neuronal systems that play a role in the recognition and estimation of numerosity:
the Approximate Number System (ANS) and the Object Tracking System (OTS). The latter is
also called Parallel Individuation System (PIS). The extent to which the OTS is an independent
system or whether more global structures play a role is still the subject of discussion (see
Chapter 5.2 in Nieder 2019).
When an individual looks at two distinguishable sets of objects, the ANS can be used to
decide which of the sets has more elements, without knowing the exact number of
elements. According to Weber-Fechner's law for sensory perception, it is not the difference
in the number of elements that determines whether a correct decision can be made, but the
relative difference (percentage). The Weber-Fechner quotient (or Weber quotient) indicates
the relative difference that can just be detected. The closer it is to 0, the better the ANS
works. The Weber quotient of the ANS can be measured free of charge on the website
panamath.org (Panamath 2010). Pictures with yellow and blue dots are shown and the test
person has to decide in a short time which of the pictures shows more dots.
The ANS is a very old neural system in evolutionary history. It can be assumed that all
vertebrates have such a system (Nieder 2019). Typical applications in nature concern swarm
behaviour (e.g. of fish or birds). When the swarm splits up, an individual will judge which
part is the larger and will join that part. Grazing animals can use their ANS to judge where
there are more interesting forage plants.
The intraparietal sulcus (IPS) is a furrow (lat. sulcus) in the parietal lobe (bilateral). In
primates, it is considered the location of the ANS and plays a central role in solving simple
computational tasks (see Chapter 6 in Nieder 2019 and Dehane et al. 2003). The IPS is also
active in visuospatial movements or controlling (see e.g. Simon et al. 2002). Through learning
experiences, the IPS increasingly forms language-independent representations of numerical
quantities (Ansari 2008, Rosenberg-Lee et al. 2009, Nieder 2019).
The algorithm or neural network underlying the ANS is unknown. Since the IPS is involved in
the control of spatial movements as well as the ANS, it can be assumed that the spatial
competencies of the IPS also play a central role for the ANS. The following model of how the
ANS functions as a neural network is speculative, see Figure 2:
1. layer: object recognition. After visual input of two sets A and B, the individual objects are
identified.
2. layer: abstraction. In a two-dimensional mental representation, recognized objects are
replaced by similar representations (A and B).
3. layer: finding pairs through spatial movement. Through spatial mental movements, the
representatives are brought together in pairs. The spatial movement of bringing the
representatives together is comparable to the coordinated spatial movements of grasping
with the hand, for example. The function of the IPS is therefore similar in both cases. Any
pair of representatives that have found each other is considered neutralized.
4. layer: interpretation. If only representatives of one type remain, or if after pairwise
neutralization an image is obtained that can be matched with a known image from memory,
then it is recognized which set has more elements.
If no result is obtained with an image in the 4th layer, it is sent back to the 3rd layer. This
process reflects the fact that ANS improves with practice. If the number of elements is very
large, the ANS fails and switches to texture matching in sections of the images.
Speculations of this kind should inspire future research or encourage the implementation of
similar networks or models with computer programs.
Figure 2. Model of the ANS
That the ANS and the OTS are in fact two different systems was shown in experiments with
infants. Feigenson Carey and Hauser (2002) conducted so-called cracker experiments on 10-
and 12-month-old babies. In these experiments, one biscuit after the other was placed in
two cups for the child to see. The child wants to eat these biscuits and indicates which cup of
biscuits he or she wants. The infants preferred (statistically significantly) 3 or 2 biscuits to
one biscuit and 3 biscuits to 2 biscuits. However, when 4 or more biscuits were placed in a
cup, the choice was made at random. This seems paradoxical because it was not recognized
that 4 was more than 1, although it was recognized that 3 was more than 1. One can assume
that in a serial experimental design (i.e. the objects are shown one after the other and not at
the same time) the OTS is activated and this is innate only for the numbers 1 to 3. As soon as
a fourth biscuit is placed in the cup, the OTS switches off, the babies thus lose their decision
support and have to choose randomly. One can assume that the OTS, unlike the ANS, is not
located alone in one location in the brain and that innate number neurons play a role in this.
Xu (2003) conducted a study in which six-month-old infants were shown dot pictures. By
observing the eyes, this simultaneous (parallel) presentation of objects revealed that 8 dots
could be distinguished from 4 dots, but not 4 dots from 2 dots, nor 2 dot from 1 dot. It can
be assumed that the ANS reacts and becomes active during parallel presentation of the
stimuli if each of the two sets has at least 4 elements. The number 4 could thus be
interpreted as the stimulus threshold for the ANS.
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