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Scarr's Hereditary-Environment Correlations

The document discusses the genetic foundations of development, emphasizing natural selection, adaptive behavior, and the role of genes in shaping human traits and psychological characteristics. It covers various genetic processes, including mitosis, meiosis, and gene expression, as well as the impact of heredity and environment on individual differences. Additionally, it addresses reproductive technologies, prenatal diagnostic tests, and the complexities of heredity-environment correlations in understanding human development.

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0% found this document useful (0 votes)
24 views5 pages

Scarr's Hereditary-Environment Correlations

The document discusses the genetic foundations of development, emphasizing natural selection, adaptive behavior, and the role of genes in shaping human traits and psychological characteristics. It covers various genetic processes, including mitosis, meiosis, and gene expression, as well as the impact of heredity and environment on individual differences. Additionally, it addresses reproductive technologies, prenatal diagnostic tests, and the complexities of heredity-environment correlations in understanding human development.

Uploaded by

bfgm69q4wj
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© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd

Evolutionary Perspective Genetic Foundations of Development

NATURAL SELECTION & ADAPTIVE BEHAVIOR COLLABORATIVE GENE

Natural Selection – an evolutionary process by which Genetic Code – information that helps us grow from one
those species who can adapt are the ones who will single cell to a person made of trillions cell.
survive and will leave the most fit offspring. Chromosomes – threadlike structures that come in 23
→ The adaptive behaviors and characteristics will pairs, with one member of each pair coming from each
be passed down to the next generation. parent.
Adaptive Behavior – behavior that promotes an organism’s → It can be found in the nucleus of the cell and it
survival in its natural habitat. contains the genetic substance DNA.
DNA – a complex molecule (double helix structure) that
EVOLUTIONARY PSYCHOLOGY
contains genetic information.
Evolutionary Psychology – emphasizes the importance of Genes – units of hereditary information and are short
adaptation, reproduction, and “survival of the fittest” in segment of DNA.
shaping behaviors.
→ These help cells to reproduce themselves and
→ “Fit” refers to the offspring of a species who can manufacture proteins that maintain life.
survive long enough to have their offspring of
Protein – building blocks of the cell and the regulator
their own.
that directs body processes.
→  chance of survival =  reproductive success
Human Genome Project – maps out the entire genetic
David Buss – emphasizes that evolution influences not
contents of our cells (linked to certain functions and
only the biological but also the psychological makeup of
developmental outcomes).
human.
→ Gene has its own location in a particular
Evolutionary Developmental Psychology – evolutionary chromosome.
psychology to understand development.
→ Major gene identification and discovery methods
→ Humans require time to develop large brains and are:
understand complexity of human society →
[1] Genome-Wide Association Method – used to
longer childhood period.
identify genetic variations linked to certain
→ Many psychological mechanisms are domain- diseases.
specific – it applies only to a specific aspect of a → Comparing the genes of a person who has a
person’s psychological makeup. certain disease to a person who don’t have
→ Brain is not a general device that can be the same disease.
applied to vast array of problems. [2] Linkage Analysis – to discover the location of
→ It evolved to process information related genes in relation to a marker gene (position of
with recurring problems experienced by our already known).
ancestors (e.g., hunting).
→ Genes passed to offspring tend to be in
→ Since evolutionary selection is primarily tied to close proximity to each other so that genes
reproductive fitness, it has not eliminated any involved in a disease are usually located
harmful conditions & nonadaptive behavior to older near the marker genes.
adults since reproduction mainly happens on the first
[3] Next-Generation Sequencing – a term used to
half of life (Paul Baltes).
describe the vast increase in genetic data
→ Alzheimer’s Disease would have been eliminated
generated at lower cost & shorter period
eons ago since this inhibits successful
compared in the past.
reproduction.
→ Entire human genome can be sequence in a → The presence of Y chromosomes in the 23rd pair
day compared before which is 10 years. determines natal sex of a person (XX in females
[4] Thousand Genome Project – the goal is to and XY in males).
→ The human genetic process creates several important
determine the genomic sequences of at least
sources of variability:
1000 individuals from different ethnic groups.
[1] The chromosomes in the zygote  chromosomes in
→ Rather than being a group of independent genes,
the mother’s ovaries/father’s testes. The
human genome consists of many genes that
chromosomes the goes into the gamete are a matter
COLLABORATE both with each other and with
of chance.
nongenetic factors inside & outside of the body.
Identical Twin (Monozygotic) – a single zygote splits
→ Gene Expression – genes can be turned on/off by
into two identical parts, creating two identical
their environment.
persons.
→ Methylation – tiny atoms attached themselves to
Fraternal Twin (Dizygotic) – two eggs are fertilized by
the outside of a gene → more or less capable of
different sperms, creating two persons w/ different
receiving & responding to biochemical signals of
genetic makeup.
body.
[2] Cellular mistake or environmental events can
GENES & CHROMOSOMES produce mutated gene – a permanently altered
segment of DNA.
→ Genes get passed down from generation to
generation (they are enduring) through three Susceptibility Genes – genes that make individual
processes: MORE vulnerable to certain diseases or accelerated
aging.
Mitosis – a cellular reproduction in which the nucleus of a
body cell divides itself into two identical parts. Longevity Genes – genes that make people LESS
vulnerable to certain disease and more likely to live
→ Each containing the same DNA as the parent’s
longer.
cells and arranged in the same chromosomal
pairs. Genotype – a person’s overall genetic materials.

46 chromosomes →
46 chromosomes Phenotype – the way a person’s genotype is expressed in
46 chromosomes
observed and measurable characteristics.
Meiosis – a form of cell division that happens in → Even though two persons are genetically
egg/sperm cells (gametes) in which the cells duplicate its identical, they may still vary in terms of physical
chromosomes and then divides twice. & psychological characteristics.
→ The end results are four cells that contain only
half of the genetic materials (only 23 unpaired GENETIC PRINCIPLES
chromosomes).
Dominant-Recessive Genes – one gene of a pair always
23 chromosomes
exerts its effects (dominant) and overrides the potential
23 chromosomes (23 chromatids)
→ influence of the other genes (recessive).
(46 chromatids) 23 chromosomes
46 chromosomes → (23 chromatids) → Only need one dominant gene to express the
(92 chromatids) 23 chromosomes trait (either from mother of father).
23 chromosomes (23 chromatids)
→ → A recessive gene needs another recessive gene
(46 chromatids) 23 chromosomes
(each one from both parents) to express itself.
(23 chromatids)
Fertilization – a stage in reproduction in which sperm and Sex-Linked Genes – most mutated genes are recessive but
egg cells fuse to create a zygote – a single fertilized egg. when this is carried on the X chromosomes → X-linked
23 chromosomes (sperm) + 23 chromosomes (egg) = 46 chromosomes inheritance.
→ Males only have one X chromosomes; males Dealing with Abnormalities:
have no backup copy to counter a harmful →
→ Not all individuals who a carry an abnormal
may develop X-linked disease.
genetic variation automatically develop that
→ Females have two X chromosomes and are not disease or mental disorder.
likely to develop X-linked disease.
→ Other genes or developmental events
Genetic Imprinting – happens when the expression of a compensate for genetic abnormalities.
gene has different effect in whether the mother or father Some Gene-Linked Abnormalities:
passed on the gene.
→ E.g., As a results of imprinting, only the
maternally derived copy of the expressed gene
might be active while the paternally derived copy
of the same expressed gene is silenced – or vice
versa.
Polygenic Inheritance – many different genes determine a
characteristic. They are collaborative and interacts to one
another to form a trait.
Gene-Gene Interaction – studies that focus on the
interdependent process by which two or more genes
influences characteristics, behaviors, diseases, and
development.

CHROMOSOMAL & GENE-LINKED ABNORMALITIES

Chromosomal Abnormalities – sometimes a gamete is


formed in which the male’s sperm/female’s ovum do not
have their normal set of 23 chromosomes.
Some Chromosomal Abnormalities:
Reproductive Challenges & Choice

PRENATAL DIAGNOSTIC TESTS

Prenatal Diagnostic Tests – used to determine whether the


fetus is developing normally or not.
Ultrasound Sonography – high-frequency sound waves are
directed into the woman’s abdomen (sound echo →
visual image of fetus’s inner structures).
→ Number of fetuses or microcephaly that can lead
to intellectual disability.
Fetal MRI – uses a powerful magnet and radio images to
generate detailed images of the body’s organ and
structures; more detailed than ultrasound.
→ Abnormalities in CNS, chest, gastrointestinal
tract, genital/urinary organs, and placenta.
Gene-Linked Abnormalities – abnormalities can be
Chronic Villus Sampling – a small sample of placenta (the
produced not only by harmful chromosomes but also by
vascular organ that links the fetus to the mother’s uterus)
harmful genes.
is removed and tested.
→ Genetic defects and chromosomal abnormalities. Closed Adoption – not having such sharing and contact.
Amniocentesis – sample of amniotic flied is withdrawn by → A choice can be offered to adoptive parents
syringe and tested for chromosomal or metabolic whether they like open or close adoption.
disorder. → Open adoption may serve the child’s best
→ Amniotic Fluid – found within amnion, a think sax interest in the long run.
un which the embryo is suspended.
Maternal Blood Screening – it identifies pregnancies that Heredity-Environment: The
have an elevated risk for birth defects. Nature-Nurture Debate
→ Spina bifida (defects in spinal cord), Down
syndrome, congenital heart disease. BEHAVIOR GENETICS
→ Also called triple screen – it measures three
Behavior Genetics – seeks to discover the influences of
substances in the mother’s blood.
heredity and environment on individual differences in
Fetal Sex Determination – sex can be determined as early human traits and development.
as 7 weeks into pregnancy.
→ Figure out the INFLUENCES that are responsible
→ Ultrasound and chorionic villus sampling in individual differences, and NOT THE EXTENT
of those influences.
INFERTILITY & REPRODUCTIVE TECHNOLOGY
→ How people vary in terms of differences in
Infertility – inability to conceive a child after 12 months genes, environment, or combination.
of regular intercourse w/o contraception. Twin Study – the behavioral similarity of identical twins
→ Can be corrected by surgery; hormone-based (genetically identical) is compared with the behavioral
drugs may improve the probability. similarity of fraternal twins.

In Vitro Fertilization (IVF) – parent’s gametes are → Twins have the struggle of developing the sense
combined in a laboratory dish → zygote → transferred of individuality (more prevalent when identical).
into woman’s uterus. → The process of moving from “WE” to “I” is a
critical task for twin children and even adults.
→  Age =  Success rate of IVF
→ Twin separation process accelerates in
→ Reproductive technologies →  multiple births
adolescence when one twin is likely to mature
→  chances of life-threatening & costly
first; also happens in emerging adulthood when
problems for babies
they go to different colleges.

ADOPTION Adoption Study – seek to discover whether the behavior


and psychological characteristics of adopted children are
Adoption – a social and legal process that establishes a
more like those of their:
parent-child relationship between persons unrelated at
[1] Adoptive parents who have provided a home
birth.
environment;
→ Three pathways to adoption:
[2] Biological parents who have contributed their
[1] Domestic adoption from the public welfare
DNA.
system
[2] Domestic infant adoption through private HEREDITY-ENVIRONMENT CORRELATIONS
agencies and intermediaries
→ Difficult to interpret results of twin and adoption
[3] International adoption
studies since it reflects the complexity of heredity-
→ Issue: whether there should be any contact with environment correlation.
children’s biological parents Heredity-Environment Correlations - individuals’ genes
Open Adoption – sharing identifying information & contact may be systematically related to the types of
with the biological parents. environments to which they are exposed.
→ Individuals inherit, seek out, or construct THE EPIGENETICS VIEW & GENE-ENVIRONMENT (G x E)
environments that may be related or linked to INTERACTION
genetic “propensities.”
→ Behavior geneticist Sandra Scarr (1993) described → Heredity-environment correlation gives heredity too
three ways that heredity and environment can be much of a one-sided influence because it does not
correlated: consider the role of prior environmental influences in

[1] Passive Genotype-Environment Correlations – occur shaping the correlation itself.

because biological parents, who are genetically → Since genes are collaborative, they do not determine
related to the child, provide a rearing environment an individual’s traits independently but in
for the child. conjunction with the environment.
[2] Evocative Genotype-Environment Correlations – occur Epigenetic View – emphasizes that development is the
because a child’s genetically influenced result of an ongoing, bidirectional interchange between
characteristics elicit certain types of environments. heredity and environment.
[3] Active (Niche-Picking) Genotype-Environment → Heredity and environment operate together—or
Correlations – occur when children seek out collaborate—to produce a person’s well-being.
environments that they find compatible and Heredity-Environment Correlations View
stimulating.
Heredity → Environment
→ Niche-Picking – finding a setting that is suited to
Epigenetic View
one’s genetically influenced abilities.
Heredity  Environment
→ Children select from their environment certain
aspects that they respond to, learn about, or Gene × Environment (G × E) Interaction – the interaction of
ignore (active selection is related to genotypes). a specific measured variation in the DNA and a specific
→ Relative importance of the three genotype- measured aspect of the environment.
environment correlations changes as children → It involves the actual molecular modification of
develop from infancy through adolescence. the DNA strand as a result of environmental
inputs in ways that alter gene functioning.
→ Specific gene  → depression; rather, gene 
stressful environment = depression.

CONCLUSIONS ABOUT HEREDITY-ENVIRONMENT


INTERACTION
→ Contributions of gene and environment are not
additive; there is no certain percentage about the
extent of their influences.
→ It is NOT accurate to say that full genetic expression
happens once.
→ Complex behaviors are influenced by genes and
environments → it gives people a propensity for a
particular developmental trajectory.
→ Development = complex gene + complex
environment.
→ Although genetic factors clearly contribute to
behavior and psychological processes, they don’t
determine these phenotypes independently from the
contexts in which they develop.

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