Lifespan Development is the study of factors that influence consistency and transformation from conception to death
Development is bidirectional, plastic and multidimensional
Adolescence was a 19th – 20th century phenomenon. compulsory schooling mid 1800s separate juvenile courts/prisons Australia 1889
Emerging Adulthood is a 21st century western phenomenon (18 to 25 years)
Developmental Influences: Cultural, historical and social
Psychoanalytic: Freud
Psychoanalytic: Erikson
Learning/Behaviourist Development Theories
Traditional Behaviourism are the theories developed by Pavlov, with classical conditioning, Watson with “little Albert”, and Skinner’s Operant Conditioning Theory
Social Learning Theory
Cognitive Development Theories
Evolutionary Theories
epigenesis: bidirectional influences of heredity and environment (including person’s own behaviour) on development
Major Development Periods
Prenatal: Conception to birth, where a one celled organism becomes a baby
Infancy: Birth to 2 years, with dramatic changes to brain and body
Early childhood: 2-6 years, motor skills, thought and language are refined and expanded
Middle Childhood: 6-11, brain develops to understand self, think logically and develop friendships
Adolescence: 11-18, abstract thought and establishing autonomy away from family
Early Adulthood: 18-40, pursuit of lifestyle - work and family
middle adulthood: 40-65, height of career and life - a developing awareness of mortality
Late Adulthood: 65-death, reflect on life, and adapt to ailing body
Genetic and environmental factors combine in intricate ways
Phenotypes: Observable characteristics of an individual, such as hair colour, height blood type
Genotype: Unique sequence of DNA - refers to two alleles am individual inherited for a particular gene
All cells within human body contain a necleus, aside from red blood cells.
Cells are the smallest unit that can live on its own. Cells make up all living organisms and tissues of the body.
Nucleus: the structure in a cell that contains chromosomes
Chromosomes: thread - like structures that contains specific instructions. Chromosomes are made up of a chemical substance called deoxyribonucleic acid, or DNA, and proteins.
A gene is a segment of DNA along the length of the
chromosome.
New individuals are created when two special cells called gametes, or sex cells—the sperm and ovum—combine. 22 of the 23 pairs of chromosomes are matching pairs, called autosomes (meaning not sex chromosomes). The twenty-third pair consists of sex chromosomes. Gametes are formed through a cell division process called meiosis, which halves the number of chromosomes normally present in body cells. When sperm and ovum unite at conception, the resulting cell, called a zygote
fraternal, or dizygotic, twins, the most common type of multiple offspring, resulting from the release and fertilization of two ova. Sometimes a zygote that has started to duplicate separates into two clusters of cells that develop into two individuals. These are called identical, or monozygotic, twins because they have the same genetic makeup
Homozygous: having identical alleles for a single trait. The child will display inherited trait
Heterozygous: Having differing alleles for a single trait.
The relationship between alleles inform Phenotype
The most common interaction between alleles is a dominant/recessive relationship. An allele of a gene is said to be dominant when it effectively overrules the other (recessive) allele.
Incomplete-dominance pattern is a form of Gene interaction in which both alleles of a gene at a locus are partially expressed, often resulting in an intermediate or different phenotype.
X-linked recessive inheritance refers to genetic conditions associated with mutations in genes on the X chromosome. A male carrying such a mutation will be affected, because he carries only one X chromosome. A female carrying a mutation in one gene, with a normal gene on the other X chromosome, is generally unaffected.
genomic imprinting, alleles are imprinted, or chemically marked through regulatory processes within the genome, in such a way that one pair member (either the mother’s or the father’s) is activated, regardless of its makeup. it is the process by which only one copy of a gene in an individual (either from their mother or their father) is expressed, while the other copy is suppressed.
mutation, a sudden but permanent change in a segment of DNA