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Campbell Chapter 13
Campbell's Biology Chapter 13 12th edition
| Term | Definition |
|---|---|
| Heredity | Transmission of traits from parents to offspring. |
| Genetics | Study of heredity and variation. |
| Gene | Unit of hereditary information made of DNA that codes for a trait. |
| Locus | Specific location of a gene on a chromosome. |
| Genome | The complete set of genetic material in an organism. |
| Somatic Cell | Any body cell except gametes; diploid (2n). |
| Gamete | Sex cell (sperm or egg); haploid (n). |
| Fertilization | Fusion of egg and sperm to form a diploid zygote. |
| Zygote | Fertilized egg; first diploid cell of new organism. |
| Asexual Reproduction | Single parent produces genetically identical offspring; uses mitosis. |
| Clone | Group of genetically identical individuals from one parent. |
| Sexual Reproduction | Two parents contribute genes to produce genetically unique offspring. |
| Homologous Chromosomes | Chromosome pairs (one from each parent) with the same genes at the same loci. |
| Diploid (2n) | Cells containing two sets of chromosomes (one maternal, one paternal). |
| Haploid (n) | Cells containing a single set of chromosomes. |
| Karyotype | Ordered display of chromosomes based on size, banding pattern, and centromere position. |
| Autosomes | Chromosomes that do not determine sex (pairs 1–22 in humans). |
| Sex Chromosomes | Chromosomes determining biological sex (X and Y). |
| Meiosis | Cell division that reduces chromosome number from diploid to haploid and produces gametes. |
| Meiosis I | First division of meiosis; separates homologous chromosomes. |
| Meiosis II | Second division of meiosis; separates sister chromatids. |
| Sister Chromatids | Identical copies of a chromosome held together at the centromere. |
| Synapsis | Pairing of homologous chromosomes during prophase I. |
| Crossing Over | Exchange of genetic material between nonsister chromatids during prophase I. |
| Chiasma (Chiasmata) | Visible site where crossing over occurred between homologous chromosomes. |
| Independent Assortment | Random orientation of homologous chromosomes during metaphase I. |
| Random Fertilization | Any sperm can fertilize any egg, increasing genetic variation. |
| Recombinant Chromosomes | Chromosomes that contain DNA from both parents due to crossing over. |
| Prophase I | Homologs pair, synapsis occurs, and crossing over happens. |
| Metaphase I | Homologous pairs line up at the metaphase plate. |
| Anaphase I | Homologous chromosomes separate; sister chromatids stay together. |
| Telophase I | Two haploid cells form, each with duplicated chromosomes. |
| Prophase II | Spindle forms in each of the two haploid cells. |
| Metaphase II | Chromosomes line up individually at the metaphase plate. |
| Anaphase II | Sister chromatids separate and move to opposite poles. |
| Telophase II | Four genetically distinct haploid cells are formed. |
| Independent Assortment Result | 2^n possible chromosome combinations in gametes. |
| Human Gamete Variation Count | About 8.4 million possible gametes (2^23). |
| Total Zygote Combinations | About 70 trillion combinations from fertilization. |
| Mutation | Original source of new genetic variations and alleles. |
| Evolutionary Importance of Variation | Allows populations to adapt and survive changing environments. |