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the dual stream hypothesis
ventral pathway - passes through the lower temporal lobes, important for understanding, connects phonological representations of sound to semantic meaning
dorsal pathway - connects the parieto-temporal cortex to the inferior frontal cortex. Important for production, is the sensorimotor interface between sound and articulatory motor centers
at 6 months - the quiet stage
peak synaptogenesis in the auditory cortex, more neural connections that are sensitive to different sound structures
at 9 months - the quiet stage
peak synaptogenesis in regions dedicated to language reception. The window for acquiring sounds natively closes, since weâre less sensitive to different sound structures
first words - 6 months
babbling begins, maturation of motor areas follows the maturation of sensory areas
first words - 10 to 12 months
infants say their first words. The motor cortex and prefrontal regions connect with the temporal lobes. This connection becomes stronger, allowing the dorsal stream to build on what the ventral stream learned.
infants show an increase in inferior frontal gyrus activation as they listen to speech across stages of development
the connections between auditory cortical areas responsive to hearing speech and those responsible for motor movements strengthens
maturation of a mirror neuron system, hypothesized to play a key role in the binding of action, perception, and language, so infants can match what they hear to the motor action necessary for production
first words - 12 to 18 months
productions are very short, 50% are nouns. At 16 months only 25% of children combine words
first words - 18 to 24 months
telegraphic two word utterances become more frequent. By 24 months, 75% of children combine words, with 33% of them being nouns.
Language production is still very rudimentary, largely without morphology. These children do not yet understand the basic syntactic categories of their language, âasyntactic integrationâ
between 14-20 months, there are clear differences in processing phonetically similar mispronunciations. By 20 months, they require exact phonetic matches, while 14 month olds do not. Â
ERP of known words vs unknown and backwards played words is lateralized to the left hemisphere by 20 months.
native language neural commitment hypothesis
the brainâs neural commitment to native language facilitates detection of native sounds and words. Strong native phonetic discrimination supports later language development
continued sensitivity to nonnative contrasts may reflect delayed specialization and does not typically facilitate native language learning. Infants who are better at discriminating native sounds produce more words at 30 months
complex forms - 18 to 32 months
EEG studies show that children are able to process syntax around this age. Ungrammatical uses of both well known and newly learned words produced an early left anterior negativity followed by a P600-like late positivity
They arenât just memorizing, theyâre actively processing syntactic rules.
complex forms - 3 to 4 years
children can ask and answer questions, demonstrating their more advanced understanding of syntax. The perisylvian regions continue to develop
complex forms - 5 years
children can talk about their experiences, desires, and goals in the past, present and future. the language system is now essentially in place. Further language development involves fine tuning. Maturation of the prefrontal areas is important for cognition and integration of these areas with perisylvian regions to optimize connections for more complex language
two types of pure alexia patients
can recognize the letters of a word but cannot read it
cannot recognize the letters of a word
visual word form area
the brainâs âletterboxâ
shows activation that depends on the degree to which a stimulus resembles a real word, it has a functional gradient in its selective activity for reading. Anterior part recruited for reading real words. Located in the left fusiform gyrus at the temporo-occipital junction
regions and structures supporting literacy
arcuate faciculus
planum temporale
other language areas including the temporal cortex and supramarginal gyrus
visual cortex
early stage
children learn a few whole words, usually proper nouns like their name
the maturation of the dorsal visual pathway (visual occipital cortex, temporal, supramarginal gyrus) allows the development of invariant visuomotor representations. which is functionally coordinated during reading
visual pathway converts letters to sounds
the left occipito-temporal region that overlaps the visual word form area still functions off the assumption of mirror invariance, children think rotation does not change letter identity
learning is transferred to the ventral pathway, so the child can learn the unique orientation of letters
the left occipito-temporal region that overlaps the visual word form area now no longer assumes mirror invariance of letters, connection of written unit to meaning
phonological stage
children learn to map graphemes to phonemes:
this stage is different lengths for different languages, depending on the opacity of the spelling system
results from the maturation of the arcuate fasciculus, which connects the visual word form area to the superior temporal and inferior parietal regions, and the planum temporale
white matter activation changes during reading and is correlated with reading skills
orthographic stage
the phonology is well mapped and spelling conventions are adopted, reading becomes automatic and fast
denser gray matter and increased connectivity between the visual word form area, the auditory areas and the planum temporale, including the arcuate fasciculus and the posterior corpus callosun
four groups of developmental disorders
neurogenetic disorders, caused by genetic abnormalities (down syndrome, williams syndrome)
behavioural disorders, defined on the basis of behavioural deficits, causes unknown (autism spectrum disorder and ADHD)
learning disability with an unknown cause - developmental disorders where the cause is not clearly genetic or environmental, they are language or reading specific (dyslexia, developmental language disorder, selective language impairment)
caused by environmental factors
down syndrome
trisomy 21
cognitive profile: significant intellectual disability
linguistic profile: expressive language is more delayed than receptive language. relatively stronger social and pragmatic skills compared to syntax
williams syndrome
deletion of genes
cognitive profile: hypersociable or âover friendlyâ personality. Strength in facial recognition, weakness in numeracy and problem solving skills
linguistic profile: delayed but eventually relatively successful development. problems in spatial prepositions, the pragmatics of conversation, and with more complex aspects of morphology
autism spectrum disorder
cognitive profile: impairments in social interaction and communication. Presence of restricted and repetitive interests or behaviours. Strong genetic component, more common in males
linguistic profile: considerable variability in language skills, 15-50% fail to acquire functional language
early linguistic signs - delay, unusual intonation and usage, 25% experienced language loss, regression
phonology - prosody and intonation is unusual, in a mechanical or exaggerated manner, with inappropriate volume or speed. Phonological differences impact prosody and social language
lexicon and syntax - inappropriate use of emotional and diectic terms, difficulty with argument structure and subject verb agreement
pragmatics
echoed language with repetitive production
idiosyncratic use of language, not abiding by conventional meanings. problems with concept formation
limited speech acts, difficulty with picking up the cues of others, moving from topic to topic and sharing interests
rigidity in language use, verbal rituals demand a particular answer from a particular person in a particular manner, irritated and upset when interruptedÂ
ADHD
delayed or atypical brain development
cognitive profile: delays in executive functioning, impacting goal directed behaviour
linguistic profile:Â
speech may be rapid, impulsive, or poorly modulated with occasional disfluencies
may produce more semantic errors and unrelated associations
complex syntax can cause comprehension difficulty
frequent interruptions, topic shifts, disorganized or tangential speech, difficulty understanding jokes, irony or indirect meanings, and poor self monitoring or conversational repair
two types of bilingualism
the ability to speak two languages
the simultaneous acquisition of two first languages
sensitive period
a period marked by increased sensitivity to certain inputs, such that learning shows a peak in efficiency and improved results
this coincides with specific neurophysiological events, like neuron formation, axonal projections, and synapses in particular brain regions. After this peak, neuroplasticity is reduced and learning therefore becomes difficult.
Most restrictive for phonology, but none for the lexicon and semantics.
bilingual brain theories
the languages depend on the same brain regions
different languages depend on different regions of the brain
some regions are specifically dedicated to bilingual functions, such as language selection, switching, and translation
all languages depend on the same regions, but there are also neural networks that differ depending on the language
brain areas involved in bilingual functions
left inferior parietal lobule - allows us to monitor the linguistic environment
anterior cingulate cortex - engages the left prefrontal cortex, especially the dorsolateral prefrontal cortex
dorsolateral prefrontal cortex and premotor area - plays a key role in attention, decisions, and inhibition, and are therefore involved in language selection
caudate nucleus - overrides one language and allows one to switch to another language
basal ganglia - projects back to the cortical structures
low proficiency activation
increased in the right hemisphere. The later the age of acquisition, the more diffuse the activation, and the more it is varied among individuals
high proficiency activation
no difference in laterality between monolinguals and this group
white matter
have observed better connectivity and increased myelin in the white matter tracts of bilingual or multilingual people compared to monolinguals
this change can take place after very little exposure to a second language, but can also disappear quickly, highly dynamic
this bilingualism related neuroplasticity leads to increased connectivity of the white matter tracts between language areas
gray matter
age of acquisition and second language proficiency affect its density in the brain due to structural reorganization
learning an L2 can cause an increase in its density in the left inferior parietal lobule and other areas involved in language processing
its density is generally negatively correlated with the age of acquisition, and is greater as L2 proficiency increases. But, the increased density is greater among school aged bilinguals than among late and early bilingualsÂ
neural reorganization triggered by bilingualism appears to follow an inverted u-shaped trajectory
initial exposure - increase in gray matterÂ
consolidation - increase in white matter connectivity, and therefore return to the gray matter norm
optimal optimization of networks, early and simultaneous bilinguals reach maximum efficiency quicker
inhibitory control
the ability to control and sustain oneâs attention, behaviour, thoughts, and/or emotions to override a strong internal predisposition or external lure, and instead do whatâs more appropriate or needed
working memory
the ability to hold information in mind and mentally work with that information to make connections or solve a problem
cognitive flexibility
the ability to change oneâs own perspective or approach to a problem, to be flexible and adjust to the demands, rules, or priorities of a task or circumstance
bilingual advantage hypothesis
suggests that bilinguals benefit from increased domain general executive functioning
cognitive reserve effects of bilingualism
can delay the onset of dementia by approximately 4.5 years
these older adults recover quicker after a stroke
functional degeneration and decline is slower
may increase with each additional language, but eventually plateaus
unclear if this is because it enhances tissue function or if the structural degeneration is just slower
attrition and the brain - pierce et al study
no behavioural differences between monolinguals, adoptees, and bilinguals at the n-back phonological working memory task, but behavioural data doesnât give the whole picture:
monolingual children showed more activation around the left lateral fissure in the insular cortex, which is a default language area.
adopted and bilingual children show more activation in the right superior temporal gyrus region, which is linked to nonverbal memory, attention, and cognitive control
on top of traditional language areas, bilinguals and adoptees recruited additional areas related ton nonverbal memory, attention, and cognitive control. The brains of adopted children more closely resembled L1 mandarin children than L1 french children, despite the fact that the adopted children no longer speak or understand mandarin
bilinguals rely on general cognitive areas, while monolinguals rely on language specific areas
french monolinguals showed more left anterior insula activation, indicating more language specific processing of french sounds by those who were exposed to french from birth.
the adoptees and bilinguals showed weaker activation with similar patterns.
they process the french sounds using a neural system originally tuned for another language
the brain can adapt and use alternative neural systems where needed
early language exposure shapes how this system develops and functions
even though an individual may appear to have completely lost their L1, âtracesâ of that native language are still present at the neural level, strongly supporting the existence of neuroplasticity and biological sensitive periods
parallel recovery
the languages are recovered at the same time and rate, most common pattern, around 60% of cases but could be higher
selective recovery
recovery of only one of the languages of a previously bilingual person
Pitreâs law - the most dominant (frequent) language recovers
Ribotâs law - the oldest language recovers
differential recovery
languages recover at the same time, but at different rates, around 18% of cases
successive recovery
the recovery of one language after the other
which language is recovered first?
the most familiar language (pitre)
the language with the highest emotional association (minkowski)
the most automated language, requiring the least effort
antagonistic recovery
a language is initially recovered, but as the other language recovers the first language is blocked.
It is possible for this recovery to alternate: the available language changes and theyâre blocked alternatelyÂ
blending recovery
uncontrollable mixing of the grammar of multiple languages, even with the intention of only speaking one language. Disrupted ability to keep languages separate, about 9% of cases