1 Chapter 2 Biological Beginnings Section 1: The Evolutionary Perspective 1. Natural Selection & Adaptive Behavior A. Natural Selection is the evolutionary process by which those individuals of a species that are best adapted are the ones that survive & reproduce B. Charles Darwin wrote On the Origin of Species (1859); Only the strong survive C. Adaptive Behavior is behavior that promotes an organism's survival in the natural habitat 2. Evolutionary Psychology A. Evolutionary Psychology - Emphasizes the importance of adaptation, reproduction, & "survival of the fittest" in shaping behavior B. David Buss points out that just as evolution shapes our physical features, such as body shape & height, it also pervasively influences how we make decisions, how aggressive we are, our fears, & our mating pattern C. Evolutionary Developmental Psychology 1. An extended childhood period evolved because humans require time to develop a large brain & learn the complexity of human society D. Evaluating Evolutionary Psychology 1. Bidirectional View: in which environmental & biological conditions influence each other. Section 2: Genetic Foundations of Development 1. The Collaborative Gene A. Chromosomes - Threadlike structures that come in 23 pairs, one member of each pair coming from each parent. Chromosomes contain the genetic substance DNA. B. DNA - A complex molecule with a double helix shape that contains genetic information. C. Genes - Units of hereditary information composed of short segments of DNA. Genes direct cells to reproduce themselves & manufacture the proteins that maintain life. D. Human Genome Project reported that humans only have about 30,000 genes (now said to be 20,500) 2. Genes & Chromosomes A. Mitosis, Meiosis, & Fertilization 1. Mitosis - Cellular reproduction in which the cell's nucleus duplicates itself with 2 new cells being formed, each containing the same DNA as the parent call, arranged in the same 23 pairs of chromosomes 2. Meiosis - A specialized form of cell division that occurs to form eggs & sperm (or gametes), each of which contains only 1/2 of the parent cell's genetic material. 3. Fertilization - A stage in reproduction whereby an egg & a sperm fuse to create a single cell, called a zygote. 4. Zygote - A single cell formed through fertilization B. Sources of Variability 1. Identical Twins (AKA monozygotic twins) develop from a single zygote that splits into 2 genetically identical replicas. 2. Fraternal twins (called dizygotic twins) develop from separate eggs & separate sperms, making them genetically no more similar than ordinary siblings 3. Genotype - A person's genetic heritage; the actual genetic material 4. Phenotype - The way an individual's genotype is expressed in observed & measurable characteristics 3. Genetic Principles A. Dominant-Recessive Genes Principle 1. The dominant gene overrides the potential influence of the other gene, called the recessive gene. This is the dominant-recessive genes principle. B. Sex-Linked Genes 1. When a mutated gene is carried on the X chromosome, the result is called X-linked inheritance. 2. Females have a backup X, making males more likely to have the X-linked disease C. Genetic Imprinting 2 Chapter 2 Biological Beginnings 1. Genetic imprinting occurs when genes have differing effects depending on whether they are inherited from the mother or the father D. Polygenic Inheritance 1. Some Chromosomal Abnormalities: The treatments for these abnormalities do not necessarily erase the problem but may improve the individual's adaptive behavior and quality of life. 4. Chromosomal & Gene Linked Abnormalities Name Description Treatment Down syndrome An extra chromosome causes mild to severe retardation and physical abnormalities Surgery, early intervention, infant stimulation, and special learning programs Incidence 1 in 1,900 births at age 20 1 in 300 births at age 35 1 in 30 births at age 45 Klinefelter syndrome (XXY) An extra X chromosome causes physical abnormalities Hormone therapy can be effective 1 in 600 male births Fragile X syndrome An abnormality in the X chromosome can cause mental retardation, learning disabilities, or short attention span Special education, speech and language therapy More common in males than in females Turner Syndrome (XO) A missing X chromosome in females can cause mental retardation and sexual underdevelopment Hormone therapy in childhood and puberty 1 in 2,500 female births No special treatment required 1 in 1,000 male births XYY Syndrome An extra Y chromosome can cause above-average height A. Chromosomal Abnormalities 1. Down Syndrome a. Down Syndrome - A chromosomally transmitted form of mental retardation, caused by the presence of an extra copy of chromosome 21. b. Appears approximately once in every 700 live births c. Women between the ages of 16 & 34 are less likely to give birth to a child with down syndrome. 2. Sex-Linked Chromosomal Abnormalities a. Klinefelter Syndrome - A chromosomal disorder in which males have an extra X chromosome, making them XXY instead of XY b. Fragile X Syndrome - A chromosomal disorder involving an abnormality in the X chromosome, which becomes constricted & often breaks c. Turner Syndrome - A chromosomal disorder in females in which either an X chromosome is missing, making the person XO instead of XX, or the 2nd X chromosome is partially deleted 1. Short in stature, webbed neck, may be infertile, may have difficulty in mathematics d. XXY Syndrome - A chromosomal disorder in which males have an extra X chromosome B. Gene-Linked Abnormalities Name Description Treatment Incidence Cystic Fibrosis Glandular dysfunction that interferes with mucus production; Physical and oxygen 1 in 2,000 births therapy, synthetic enzymes, 3 Chapter 2 Biological Beginnings breathing and digestion are and antibiotics; most hampered, resulting in a shortened individuals live to middle life span age Diabetes Body does not produce enough insulin, which causes abnormal metabolism of sugar Early onset can be fatal unless treated with insulin 1 in 2,5000 births Hemophilia Delayed blood clotting causes internal and external bleeding Blood transfusion/injections 1 in 10,000 males can reduce or prevent damage due to internal bleeding Huntington Disease Central nervous system deteriorates, producing problems in muscle coordination and mental deterioration Does not usually appear until age 35 or older; death likely 10 to 20 years after symptoms appear 1 in 20,000 births Phenylketonuria Metabolic disorder that, left (PKU) untreated, causes mental retardation Special diet can result in average intelligence and normal life span 1 in 10,000 to 1 in 20,000 births Sickle-Cell Anemia Blood disorder that limits the body's oxygen supply, it can cause joint swelling, as well as heart and kidney failure. Penicillin, medication for pain, antibiotics, and blood transfusions 1 in 400 African American children (lower among other groups) Spina bifida Neural tube disorder that causes brain and spine abnormalities Corrective surgery at birth, orthopedic devices, and physical/medical therapy 2 in 1,000 births Tay-Sachs Disease Deceleration of mental and Medication and special diet physical development caused by an are used, but death is likely accumulation of lipids in the by 5 years of age nervous system 1 in 30 American Jews is a carrier 1. Phenylketonuria (PKU) - A genetic disorder in which the individual cannot properly metabolize phenylalanine, an amino acid. PKU is now easily detected- but if left untreated, results in mental retardation & hyperactivity 2. Sickle-Cell Anemia - A genetic disorder that affects the red blood cells & occurs most often in African Americans C. Dealing with Genetic Abnormalities Section 3: Reproductive Challenges & Choices 1. Prenatal Diagnostic Tests A. Ultrasound Sonography 1. Ultrasound Sonography is a prenatal medical procedure in which high frequency sound waves are directed into the pregnant woman's abdomen. The echo from the sounds is transformed into a visual representation of the fetus' inner structure B. Fetal MRI 1. Can provide more detailed images than ultrasound C. Chronic Villus Sampling 1. A prenatal medical procedure in which a small sample of the placenta is tested D. Amniocentesis 4 Chapter 2 Biological Beginnings 1. A prenatal medical procedure in which a sample of amniotic fluid is withdrawn by syringe & tested for chromosomal or metabolic disorders E. Maternal Blood Screening F. Noninvasive Prenatal Diagnosis (NIPD) 2. Infertility & Reproductive Technologies A. Approximately 10-15% of couples in the US experience infertility 3. Adoption A. Children who are adopted very early in their lives are more likely to have positive outcomes than children adopted later in life. B. Adopted children showed more behavioral problems than nonadoptees C. Adopted children are more likely to have a learning disability than nonadopted children D. Adopted children perform lower in school despite similar IQ & cognitive development to their nonadoptive counterpart Section 4: Heredity & Environment Interaction: The Nature-Nurture Debate 1. Behavior Genetics A. Behavior Genetics - The field that seeks to discover the influence of heredity & environment on individual differences in human traits & development B. Twin Study - A study in which the behavioral similarity of identical twins is compared with the behavioral similarity of fraternal twins C. Adoption Study - A study in which investigators seek to discover whether the behavior & psychological characteristics of adopted children are more like their adoptive parents, who provided a home environment, or more like their biological parents, who contributed their heredity. Another form of the adoption study is to compare adoptive & biological siblings 2. Heredity-Environment Correlations A. Heredity-environment correlations means that individuals' genes may influence the types of environments to which they are exposed B. Passive Genotype-Environment Correlations - Correlations that exist when the biological parents, who are genetically related to the child, provide a rearing environment for the child C. Evocative Genotype-environment Correlations - Correlations that exist when the child's genotype elicits certain types of physical & social environments D. Active (Niche-Picking) Genotype-Environment Correlations - Correlations that exist when children seek out environments they find compatible & stimulating HeredityEnvironment Correlation Description Examples Passive Children inherit genetic tendencies from their parents, and parents also provide an environment that matches their own genetic tendencies Musically inclined parents usually have musically inclined children and they are likely to provide an environment rich in music for their children Evocative The child's genetic tendencies elicit stimulation from the environment that supports a particular trait. Thus genes evoke environmental support A happy, outgoing child elicits smiles and friendly responses form others Active (nichePicking) Children actively seek out "niches" in their environment that reflect their own interests and talents and are thus in accord with their genotype Libraries, sports fields, and a store with musical instruments are examples of environmental niches children might seek out if they have intellectual interests in 5 Chapter 2 Biological Beginnings books, talent in sports, or musical talents, respectively 3. Shared & Nonshared Environmental Influences A. Shared Environmental Experiences - Siblings' common environmental experiences, such as their parents' personalities & intellectual orientation, the families socioeconomic status, & the neighborhood in which they live B. Nonshared Environmental Experiences - The child's own unique experiences, both within the family & outside the family, that are not shared by another sibling. Thus, experiences occurring within the family can be part of the "nonshared environment" 4. The Epigenetic View A. Epigenetic View - Emphasizes that development is the result of an ongoing, bidirectional interchange between heredity & environment.