lecture notes Flashcards

1
Q

correlation

A

strength of the association between two variables

  • vale (r) can range from -1.0 to 1.0
  • value of 0.0 means its not correlated
  • closer to 1 or -1 the stronger the correlation
    • or - determines direction

correlation does not equal causation
- relationship may be due to a third variable

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2
Q

what’s the solution to determine causal relationships?

A

“true” experiments

  1. random assignment to different conditions
    - pre-existing differences between people recruited for the different groups in your experiment will be randomized and “wash out”
  2. control over what is experienced
    - good experimental design will have people in different conditions experience the exact same conditions, except for a manipulation
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3
Q

reliability

A

The degree to which a given
measure is consistent with
each measurement.

  1. Interrater Reliability
  2. Test-Retest Reliability
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4
Q

validity

A

The degree to which a given
measure is capturing the
construct it is proposed to
be measuring.

  1. Internal Validity
  2. External Validity
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5
Q

a measure can be reliable

A

but not valid, but a measure can only be valid if it is reliable

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6
Q

contexts for collecting data

- interviews

A

pros

  • provides insight into subjective experiences of individuals
  • technological advancements making this more feasible

cons

  • time consuming; less feasible to administer on larger scales
  • generally low interrater reliability
  • questionable utility for predicting future behaviours
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7
Q

contexts for collecting data

- naturalistic observation

A

pros

  • provides insight into “real world” behaviours
  • technological advancements making this more feasible

cons

  • time consuming; less feasible to administer on larger scales
  • experimenter presence disrupts “natural” environment
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8
Q

contexts for collecting data

- LENA device

A
  • captures vocalizations in home
  • special algorithms used to analyze speech patterns and non-speech vocalizations
    • number of words spoken near the child
    • number/length of speaking turns
    • time spent in activities (TV; car rides; sleep; play)
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9
Q

how can we study the development of a child in a laboratory experiment?

A
  • cross- sectional: recruit different age groups
  • longitudinal: follow same individuals over time
  • microgenetic: focused on studying children at developing times. - longitudinal
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10
Q

cross-sectional designs

A
  • compare children from different age groups on same measure
  • however, must consider validity of measure across age groups
  • doesnt allow you to track individual differences over time
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11
Q

longitudinal designs

A
  • get a measure from the same group of children over time
  • address how individual differences change through lifespan
  • difficult to follow children over time; very time consuming (may be more difficult to get grant funding over time)
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12
Q

longitudinal designs interventions

A
  • leverages strengths of longitudinal design and experimental control
  • randomized control trials (RCTs): randomly assign participant to a group that receives a treatment or to a control group
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13
Q

microgentic designs

A
  • study a developing process at the age it is proposed to change
  • similar to a longitudinal design, but shorter period
  • elucidates the mechanisms of change
  • allows for analyzing individual differences in change
  • over shorter period of time
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14
Q

high-amplitude sucking

A
  • pacifier connected to computer
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15
Q

Common devo. DVS (measures)

A
  1. high-amplitude sucking
  2. preferential looking
  3. normative assessments
    4, neuroimaging
    a) structural (MRI, DTI)
    b) functional (EEG, fMRI)
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16
Q

High amplitude sucking

A
aka. non-nutritive sucking 
✴Pacifier connected to computer
✴Measures changes in air pressure 
that occur with sucking
✴Sucking rate reflects level of 
interest in given stimuli
     ✴Increased sucking rate with 
         increased interest
       ✴Bored infants show much 
           decreased sucking rate
✴Successful method for studying 
infants as young as 8-hours-old
✴Present a sound every time infant increases sucking 
rate beyond a given threshold (e.g. 80% increase)
✴If sucking rate increases in order to listen to a certain 
sound, infant prefers the sound (i.e., speech)
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17
Q

preferential looking

A

✴Looking time at an object equated to preference
✴When presented with similar stimuli, longer looking at one than the other indicates ability to discriminate

Uses: Eye-tracking Cameras

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18
Q

Head-Turn Preference

A

✴Similar to preferential looking, but with sound stimuli
✴Assumed that children turn their heads towards
sound sources they perceive as novel
✴Used as an index of detecting a change in stimuli

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19
Q

Head-Turn Preference

- how to test

A

Light in the center blinks to get fixation
- light goes out when child looks

light starts blinking either on left/right

  • when the child looks at light, a sound is played
  • sound stops when child looks away

or child looks at center and play new sounds to either side
- looking to new sound indicates detection of change

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20
Q

Normative Assessments

A

Standford-Binet intelligence scales

  • ages 2 to 85+ years old
  • measures verbal and nonverbal abilities
  • normative scores, M= 100, SD= 15
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21
Q

Normative assessment

subscales:

A
  • fluid reasoning
  • knowledge
  • working memory
  • quantitative reasoning
  • visuospatial processing
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22
Q

Normative assessment

Wisconsin card sorting task

A
  • “Set-shifting”- rules for sorting change throughout
  • diagnostic for children and older adults
  • generally measures frontal lobe function
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23
Q

Neuroimaging

Structural measures

A
  • magnetic resonance imaging (MRI)

- Diffusion tensor imaging (DTI)

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24
Q

neuroimaging

Functional measures

A
  • Functional MRI (fMRI)
  • Electroencephalogram (EEG)
  • Event-related Potentials (ERPS)
  • Magnetoencephalogram (MEG)
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25
Q

Magnetic Resonance Imaging (MRI)

A
  • great spatial resolution (-1mm)
  • great soft tissue contrast
    - white vs. gray matter
  • no ionizing radiation (as in x-rays)
    - measure depends on magnetic
    properties of hydrogen
    - MRI machine creates powerful
    magnetic field (teslas)
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26
Q

Diffusion Tensor Imagining (DTI)

A
  • utilizes same machine as MRI (different “scan”)
  • measures diffusion of water within the brain
  • used to image structure of white matter connectivity
  • tractography: which regions are connected and by what fibers?
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27
Q

functional MRI (fMRI)

A
  • same machine as MRI but different ‘scan’ during task
  • measures changes in blood flow
    • BOLD: blood oxygenation level dependent signal
    • more oxygen used by areas that are active
  • requires contrast between conditions (task of interest vs. resting baseline)
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28
Q
functional MRI (fMRI)
advantages / disadvantages
A

advantages

  • great spatial resolution (-3mm)
  • noninvasive and relatively child-friendly

disadvantages

  • poor temporal resolution (~6-10 seconds)
  • disrupted by movement
  • very expensive
  • very loud
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29
Q

Electroencephalogram (EEG)

A
  • raw EEG from electrodes in a cap placed on my head

1) put cap on head
2) put gel in buttons
3) place electrodes

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30
Q

Event-related brain potentials (ERPs)

A
  • average on-going EEG by stimulus type
  • time-locked to the onset of a specific stimulus

multiple measures:

  • amplitude (How much)
  • latency (when)
  • scalp distribution (where)
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31
Q

Event-related brain potentials (ERPs)

advantages/ disadvantages

A

advantages:

  • excellent temporal resolution (ms)
  • noninvasive and very kid friendly

disadvantages:

  • poor spatial resolution
  • disrupted by motion and eye artifact
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32
Q

magnetoencephalogram (MEG)

advantages/ disadvantages

A

advantages:
- spatial resolution ~ MRI with temporal resolution of EEG

disadvantages

  • cannot image subcortical areas
  • very expensive
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33
Q

brief history of genetics

A

Father of modern Genetics

  • Gregor Mendel (1822-1884)
  • Austrian Monk
  • Studied pea plants

examined

  • flower color. position
  • seed color, shape
  • pod color, shape
  • stem length

noticed that cross-breeds did not have intermediate stages of traits

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34
Q

Mendel’s Theory

A
  • pea plants can self- or cross- pollinate
  • cross-pollination of purebred parents followed by self-pollination for several generations
  • first generation all had the same traits
  • second generation had some of one trait and some of the other.. but no mixing
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35
Q

Mendel’s Theory

Dominant-recessive patterns

A

homozygous - same two alleles present
heterozygous- two different alleles
- if heterozygous, only one of the traits will be expressed (dominant)
- but heterozygous gene could combine with a recessive gene later to produce the recessive trait

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36
Q

Mendelian Patterns

A
  • few human traits follow this simple pattern; most genes= multiple traits
  • both alleles/blending can be expressed
  • genes inherited from mother vs. father may be expressed differently
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37
Q

Deoxyribose Nucleic Acid

A
  • genes: sets of chromosomes that are the basic unit of heredity in all living things
    • carry the code for proteins
  • regulatory genes control activity of other genes
  • genes are continually turned on/off during life
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38
Q

Allelic variation

A
  • variability in certain genes exist in the population
  • 5 HTT: serotonin transporter gene
    • long allele: greater serotonin transporter transcription
    • short allele: less transcription- may be more susceptible to pathologies, yet may offer cognitive advantage
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39
Q

We are family

Genetic similarity with:

A
other humans: 99,9%
chimps/bonobos: 98.8%
orangutan: 96.9%
rhesus monkey: 93.0%
cats: 90.0%
sea sponge: 70.0%
bananas: 50.0%
bacteria: 25.0%
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40
Q

genotype vs. phenotype

A

genotype: inherited genetic materials

phenotype- observable characteristics of the genotype

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41
Q

epigenetics

A
  • genes are modified by experience

- modifications can be inherited by offspring

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42
Q

mechanisms of epigenetic signaling

A
  • methylation can alter the expression of a given gene
  • changes in methylation occur with experience and are heritable
  • more nurturance increases ability to dampen HPA stress response
  • —– removes methyl groups from gene linked to cortisol receptors
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43
Q

behavioural genetics

A
  • we know that environment affects gene expression but we typically cant manipulate environment
  • different environment can lead to different outcomes for individuals with the same genes
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44
Q

Dominant vs recessive phenotypes

A

Dominant

  1. curly hair
  2. full head of hair
  3. dark hair
  4. thick lips
  5. cheek dimples
  6. farsightedness
  7. type A or B blood
  8. Rh+ blood

Recessive

  1. straight hair
  2. pattern baldness
  3. blonde hair
  4. thin lips
  5. no dimples
  6. nearsightedness
  7. type O blood
  8. Rh- blood
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45
Q

genetic disorders

- recessive alleles

A
  1. albinism
  2. cystic fibrosis
  3. phenylketonuria (PKU)
  4. Tay-Sachs disease
  5. Sickle-cell disease
46
Q

other genetic disorders

A
  1. huntington’s disease
    - dominant allele on chromosome 4
  2. down syndrome
    - extra 21st chromosome
  3. hemophilia
    - gene carried on the X chromosome
    - more prevalent in males (XY)
    - females (XX) can be buffered by dominant allele
47
Q

prenatal development stages

A
  1. conception
  2. zygote
  3. embryo
  4. fetus
48
Q

conception

A

occurs when egg and sperm meet in the fallopian tube

  • each parent provides a gamete (egg/sperm)
      • 23 chromosomes each = 46 total
      • only 23rd chromosome differs by gender
49
Q

largest human cell

smallest human cell

A

the egg is the largest

the sperm is the smallest

50
Q

only __ sperm survive the __ hour voyage

A

200

~6 hour

51
Q

nuclei of egg and sperm merge into a

A

zygote

52
Q

zygote

A
  • a fertilized egg cell (46 chromosomes)
  • rapid cell division begins to take place
  • zygote tuns into blastocyst (~100 cells)
  • “Germinal stage” ends when implanted into uterine wall (~ 2 weeks)
53
Q

embryo

embryonic stage

A

weeks 3-8

54
Q

embryonic stage`

  • cell division
  • cell migration
  • cell differentiation
  • cell death
  • hormones
A

• Cell division: from 1 to trillions of cells in 38 weeks
• Cell migration: movement of newly formed cells to destination
• Cell differentiation: specialization of cells for given function
• Cell death: genetically programmed death of some cells
• Hormones: sexual differentiation; fetus regulates own development.
Embryo`

55
Q

embryo formed from

A

inner cell mass of zygote folding into 3 layers

56
Q

neural tube

A

one end becomes brain, other end becomes spine

57
Q

ectoderm/ mesoderm/ endoderm

A
  • ectoderm: nervous system, inner ear, eye lens, outer layer of skin, nails, teeth
  • mesoderm: muscles, bones, circulatory system, inner layers of skin, internal organs
  • endoderm: digestive system, lungs, urinary tract, glands
58
Q

amniotic sac
placenta
umbilical chord

A
  • amniotic sac: fluid-filled membrane around embryo and later, the fetus
  • placenta: semi-permeable organ that allows exchange of materials in mother’s blood to the fetus
  • umbilical chord: connection of blood vessels between mother and fetus (to/from placenta)
59
Q

fetal stage weeks

A

weeks 9-births

60
Q

cephalocaudal development

A

areas closer to the head develop earlier than areas farther from the head

61
Q

Fetus
sensory development
- touch/ taste/ smell/ hearing

A
  • touch: feels its own body- face, fingers, umbilical cord
  • taste: amniotic fluid flavor varies with mother’s diet
  • smell: amniotic fluid smell varies with mother’s diet
  • hearing: fetal environment is noisy
62
Q

teratogens

A

external agents that damage prenatal environment

  • damage dependent on critical period of exposure
  • dose-response relationship
  • Can be stress not just substances such as drugs and alcohol
63
Q

maternal factors

A
  • age: <15 & >35 years
  • nutrition: low folic acids
  • disease: rubella, STDs
  • emotional state: perceived stress: fetal heart rate associated with mother’s self-reported distress
64
Q

prenatal brain development

- first 4 weeks after conception

A

outermost layer of embryonic cells -> neural plate -> neural groove -> neural tube

65
Q

neural tube development

A
  • neural tube differentiates into 3 parts

- complete by 8 weeks

66
Q

neural tube defects

A

ex. spina bifida
- ~1 in 1000 live births in US
symptoms
- leg paralysis
- orthopedic abnormalities
- reading disabilities
- difficulties with executive function skills
- other cognitive deficits

diet rich in folic acid linked to prevention of spina bifida

67
Q

major development milestones

A

4-8 weeks: hemispheres of cerebral cortex emerge

8-26 weeks: cerebral cortex grows to cover midbrain

~28th week: cortical surface area expands, begins to fold
- most neurons you will have are now present

28-40 weeks: gyri and sulci of the brain begin to develop

68
Q

neurogenesis

A
  • formation of new neurons - almost complete by 18 weeks gestation

neural migration

  • neurons move from innermost layers of tissue outward via glial cells
  • cells formed earlier stay closer to their origination
  • results in layers in the brain
69
Q

neuronal migration defects

A
  • misplaced or oddly formed neurons
  • childhood epilepsy
  • intellectual disabilities
  • schizophrenia, dyslexia, and autism may be caused by mutations in genes that control neural migration
70
Q

neural differentiation

A
  • cell type is specific to a given area of the brain

- followed by synaptogenesis and dendritic branching

71
Q

myelination

A
  • insulates the axon- faster communication
  • formed by glial cells- outnumber neurons 10:1
  • begins in the 3rd trimester, continues through life
72
Q

synaptogenesis

A
  • formation of synapses between neurons

- huge growth from ~prenatal week 28 to ~2 years

73
Q

synaptic pruning

A
  • “use it or lose it”
  • connections maintained are experience-based
  • axons withdrawal and dendritic spine it synapsed on is pruned away
  • neuroplasticity
74
Q

frontal lobe
parietal lobe
temporal lobe
occipital lobe

A

frontal: executive function (planning, attention)
parietal lobe: spatial processing, information integration, somatosensation
occipital: vision
temporal lobe: audition, memory, emotion processing

75
Q

postnatal brain development

A
  1. different neural components have different developmental trajectories
    - gray matter decreases with age
    - white matter increases into mid-adulthood then decreases- u- shaped curve
    - cerebrospinal fluid (CSF) increases with age
  2. different brain regions have different developmental trajectories
    - regions for sensory functions mature early (visual and auditory cortex: limbic regions)
    - regions for higher-order functions mature later - frontal lobe (executive function); posterior parietal
  3. high degree of individual variability in development
    - interaction of genes and experiences (neuroplasticity)
    - brain uses input to fine-tune neural circuitry

pros:
- reduces the number of genes needed for development
- allows or better recovery from brain injury - younger brains generally heal better

cons:

  • “double-edged sword” of neuroplasticity
  • systems that re most susceptible to deficit with atypical experiences
    • early cataracts- pruning of visual cortex
    • language deprivation in feral children
76
Q

Neuroplasticity and ASL

  • participants
  • task
A

participants

  • native English speakers
  • deaf native american sign language signers
  • control group- hearing native ASL signers

task

  • reading: English sentences vs. consonant strings
  • viewing: ASL sentences vs. meaningless signs.
77
Q

Sensitive periods

- timing of experience is key

A
  • neural organization of different areas occur during specific periods in development
  • lack of stimulation during that period can alter brain function and may be irreversible

examples:

  • vision and hearing- very early in life
  • phonology- within first year of life
  • language- within first 5-7 years of life
78
Q

experience-dependent plasticity

A
  • neural connections created and reorganized throughout life based on individual experiences
    • types of experiences you have shape your bran structure and function
      ex. music, language, motor activities.
79
Q

infant vision

A
  • newborns prefer to look at stuff (than not stuff)
  • habituation as an indicator of change detection

infants will likely spend less and less time looking at a repeated stimulus ..
but when the stimulus changes, looking time will increase if change was detected.

  • less light strikes fovea
    • 2% of all light (adults, 65%)
    • 20/120 vision, or worse, in 1st month

less color experienced
1st month: shades of white
2-3 months: adult-like color perception
4-5months: adult like color preference

80
Q

cones approach adult functionality at what age

A

8 months of age

81
Q

visual acuity

A
  • lens focus better by 3 months
  • approaching adult levels by 8 months
  • not fully adult-like until 6 years of age
82
Q

visual scanning

A
  • infants look around from birth
  • tracking difficult because eye control and coordination are poor
  • tracking becomes smoother by 2-3 months (if slow object)
  • in 1st 2 months: only scanning one part or outer edges
  • by 2 months - begin scanning entire object/ attention to overall shape and major details
83
Q

Face perception

A
  • from birth, infants show preference for human faces
  • within 12 hours of exposure, an infant prefers image of mother
  • can discriminate amongst facial expressions by 4 months
  • by ~ 9 months, infants develop a prototype for faces they see
  • – less able to discriminate between faces of other species, unless trained
  • – 3 months old prefer female faces, unless father is primary caregiver
  • – perceptual narrowing by experience
84
Q

infant audition

A

sound processing

  • hearing not adult-like until 5-8 years
  • newborns tend to turn towards sound (as early as 10 min old)
  • head-turn procedure
85
Q

infant audition

- music processing

A
  • infants pay more attention to consonant sounds than dissonance
  • by 4.5 months, listen longer to melodies with pauses inserted in natural gaps (vs. unnatural gaps)
  • by 5 months, recognize melody played at higher or lower pitch- remain habituated after familiarization
86
Q

infants preference for taste

A

sweets

87
Q

infants preference for smell

A

two-week olds prefer smell of their mom over a different woman

88
Q

intermodal perception

  • oral + visual
  • tactile + visual
  • audio + visual
A

oral + visual
- newborns and 1 month olds look longer at pacifier they had sucked on but hadn’t seen

tactile + visual
- 4-month-olds recognize rings they had explored with hands but hadn’t seen

audio + visual

  • 4-month-olds prefer videos that match audio track
  • 5-month-olds match facial expression to emotion
89
Q

motor dev.- reflexes

A
grasping (palmar)
tonic neck
rooting
sucking
babinski, moro, blink, stepping, and withdrawal
90
Q

disappearing reflexes

A
  • stepping reflex usually disappears by 2 months old - unless given extra practice at this age
  • leg fat grows faster than muscles do, until ~7 months
  • – infants step more if supported by water buoyancy
  • – younger infants step less if legs weighted down
91
Q

Motor Milestones

A
  • pre-reaching
  • sitting & reaching
  • crawling
  • walking
92
Q

cliff crawl

A
  • infants will crawl over glass floors looking like a “cliff” until they have ~1 month experience with crawling
  • when first crawling and waking, infants misjudge slopes that they are able to navigate safely - also influenced by social cues from caregiver
93
Q

Mothers that experience more stress also show that

A

the fetus has an elevated heart rate as well

94
Q

Can never go wrong with having too much

A

folic acids- the developing brain needs this fatty acid for developing brain cells and nerves that are lined with fatty layers

95
Q

Neural tube development

- follic acid

A
  • Clinical trials have shown that increasing your diet with folic acids can prevent spina bifida (prenatal vitamins)
96
Q

forebrain becomes

A

CNS

97
Q

You have more brain cells as a

A

fetus than you ever will as an adult

o The white matter is what develops and grows – newborn to 2 years

98
Q

Glial cells

A

neuron travel along the glia to get where they want to get in the cortex.

99
Q

Synaptic pruning

A
  • Happens around 5 to 6 years of age
  • When pruning happens you often maintain connections that have been solidating.
    o Typically skills we have expertise
  • The brain is most flexible around age 4 (between 5-6 years)
    o Train them around then so these skills are most likely to remain past the pruning event
100
Q

Different areas of the brain mature at

A

different time points

101
Q

A fully mature profile occurs around

A

26- the brain is still plastic and changeable though
- Sensory functions mature faster (visual and auditory)
o Don’t want to fully develop your ability to regulate and express higher order behaviours until you have experienced more things
o But visual and auditory are necessary

102
Q
  • Information goes in from your eyes to the back of your brain at the occipital lobe
A

o Using dorsal and ventral pathways information is sent throughout the rest of the brain
 Information first goes to the temporal lobe where we go through our memories to see if we recognize what we are seeing
o Visual information will also travel upwards to the parietal lobe to tell us how things are moving
 Spatial processing information
 Sensations on your fingers and other parts of body that have spatial sensitivity light up in the front of the parietal lobe
o Cerebellum- balance – important

103
Q

Eric Courchesne Autism Brain Growth video

A
  • Understanding causes of autism
  • Discovered a phenomenon; early brain overgrowth – brain in autism grows too large too fast at a very young age
    o The brain gets too big – if they can figure out why the brain does this, they can help kids
    o Looked at brain cells that grow in the frontal cortex (important for social communication – doesn’t work very well In beginning stages of autism)
    o There is a 67% of over abundance of brain cells in the frontal cortex –
     Probably means there is excess wiring- failure for this part of the brain to help the child learn communication skills
     Need to change the course of the wiring patterns
104
Q

When people are speaking in sign language there is a similar neuro pattern of activation

A

that can be seen in the brain when people are communicating to you verbally or through writing
- Late learners of ASL do not have right hemisphere activation
- Brains wiring for language really depends on your early experience
o Areas of the brain that represents language are plastic and malleable with experience

105
Q

Over time there is a phenomenon called habituation – visual processes get

A

maxed out from seeing something for so long. (keeps seeing screen with black dashes) – if colour changes, they get reinterested

106
Q

`cones process

rods process

A
  • Cones are the cells in the middle of the eye – process colour
  • Rods- process brightness 0 develop earlier
    o Start with like black and white vision
107
Q

Visual acuity

- Refers to how

A

sharp your vision is
- You want to put your face up real close to the enfant when talking to them so they have a chance at seeing your face and smile

108
Q

Visual scanning

-infants dont have the higher brain function

A

to control their eyes like adults do

- In 1 month they can habituate between triangle and square

109
Q
  • Palmar reflex (grasping):
  • Tonic neck:
  • Rooting:
  • Sucking:
  • Babinski
  • Moro reflex
A
  • Palmar reflex (grasping): if you put something straight on an infant hand, they will grab onto it
  • Tonic neck: place a baby down on their back and they will typically shift their weight and their arm will stick out in the direction they are looking
    o Supports the neck
  • Rooting: stroke and infants’ cheek or put something near their mouth and they will think it’s a nipple and root towards it
  • Sucking: natural reflex’s
  • Babinski: stroke bottom of foot- toes span out
  • Moro reflex: holding baby and you make their weight drop a little- their arms will reach out
110
Q

Crawling motor milestone is usually there by

A

10 months

111
Q

Walking milestone occurs

A

11-12 months