BPB 217 Week 4: Heritability and Biological Basis of Intelligence

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A set of vocabulary flashcards covering heritability, biological markers of intelligence, developmental theories, and medical conditions affecting cognitive function.

Last updated 9:52 AM on 4/30/26
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24 Terms

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Heritability (h2h^2)

The proportion of observed differences in a trait among individuals in a population that is due to genetic variation.

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Monozygotic (MZ) Twins

Identical twins who share 100%100\% of their DNA, used in behavioral genetics to study the role of genes in intelligence.

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Dizygotic (DZ) Twins

Fraternal twins who share approximately 50%50\% of their DNA, similar to ordinary siblings.

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Parieto-Frontal Integration Theory (P-FIT)

A neurological model proposed by Jung and Haier (20072007) stating that intelligence depends on the efficient interaction of the parietal lobes, frontal lobes, and white matter pathways.

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Neural Efficiency Hypothesis

Proposed by Richard Haier, this hypothesis suggests that high-IQ individuals show lower glucose metabolism during cognitive tasks, using less energy for better results.

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Processing Speed

A biological correlate of intelligence (r0.300.50r \approx 0.30 - 0.50) reflecting the quality of basic neural transmission and myelination.

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Dopamine

A neurotransmitter that regulates prefrontal cortex function, working memory, and executive control; dysregulation is associated with ADHD.

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Acetylcholine

A neurotransmitter important for learning, memory formation, and attention that is reduced in Alzheimer’s disease.

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Flynn Effect

The steady rise in average IQ scores observed throughout the 20th20\text{th} century, approximately 33 IQ points per decade.

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Active GxE Correlation

A gene-environment interaction where individuals with higher genetic potential seek out more stimulating environments.

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Scarr-Rowe Interaction

The finding that heritability of intelligence is higher in affluent environments and lower in deprived environments, where poverty acts as a suppressor.

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Fetal Alcohol Spectrum Disorder (FASD)

The most common non-genetic cause of intellectual disability, caused by prenatal alcohol exposure resulting in permanent brain damage.

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Congenital Hypothyroidism

A condition that causes severe intellectual disability if untreated, but is reversible with early thyroid hormone replacement.

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Lead Poisoning

Environmental toxin exposure where each 10μg/dL10\,\mu g/dL increase in blood lead is associated with a 151 - 5 point IQ reduction.

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Fragile X Syndrome

The most common inherited cause of intellectual disability, typically more severe in males.

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Sensorimotor Stage

Piaget's stage (020 - 2 years) where intelligence is expressed through physical action and the development of object permanence.

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Zone of Proximal Development (ZPD)

Vygotsky's concept of the gap between what a child can do alone and what they can achieve with guidance.

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Scaffolding

The support provided by a more knowledgeable person to help a child accomplish tasks, which is gradually removed as competence grows.

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Working Memory

The ability to hold and manipulate information in mind simultaneously; a strong predictor of academic achievement and IQ.

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Fluid Intelligence (Gf)

The capacity to reason and solve novel problems without prior knowledge; it peaks in early adulthood (\approx age 2525) and then declines.

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Crystallised Intelligence (Gc)

Accumulated knowledge, vocabulary, and skills learned through experience that typically grows or remains stable through adulthood.

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Cognitive Reserve

The brain's resilience to neurological damage, built through education, demanding occupations, and mental stimulation.

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Intellectual Disability (ID)

A neurodevelopmental condition characterized by an IQ below 7070, limitations in adaptive behavior, and onset before age 1818.

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Mild Intellectual Disability

A classification for individuals with an IQ range of 557055 - 70, comprising approximately 85%85\% of cases.