Students taking introductory biology can download the complete textbook “Biology 2e” by Mary Ann Clark, Jung Choi, Matthew Douglas, and contributors, free as a PDF from OpenStax. It is a two-semester, 47-chapter sequence covering the chemistry of life, cell biology, genetics, evolution, biological diversity, plant biology, animal anatomy and physiology, and ecology — the standard foundation for BS Biology, Pre-Medical, and related programs.
Because 47 chapters is a lot to list one at a time, this page groups them into 8 topic blocks — matching the book’s own 8 official Units exactly: The Chemistry of Life, The Cell, Genetics, Evolutionary Processes, Biological Diversity, Plant Structure and Function, Animal Structure and Function, and Ecology — each naming every real chapter number and title it contains in full. The book itself is untouched; this is purely a page-layout choice to keep a 47-chapter book readable on one page.
Book Overview
| Course | Biology I & II (two-semester, introductory biology sequence) |
| Degree Programs | BS Biology, Pre-Medical, Biochemistry, Environmental Science, and any STEM program requiring introductory biology |
| Level | University — two-semester introductory biology course |
| Edition | OpenStax 2nd edition — published March 28, 2018 |
| Author | Mary Ann Clark, Jung Choi, Matthew Douglas, and contributors (OpenStax) |
| Structure | 47 chapters, grouped into 8 topic blocks below, matching the book’s own 8 official Units — Units I–III (Chemistry of Life, The Cell, Genetics) typically form Biology I, and Units IV–VIII (Evolutionary Processes, Biological Diversity, Plant Structure and Function, Animal Structure and Function, Ecology) typically form Biology II |
| Exercises | Every section includes Visual Connection questions, Art Connection questions, and end-of-chapter Review Questions, Critical Thinking Questions, and a Chapter Summary |
| Language | English |
| License | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 (CC BY-NC-SA 4.0) — Model: Link-only |
| Format | Free PDF and web/HTML reader; also available as a low-cost print edition through third-party printers |
Chapter List
Topic Block 1: The Chemistry of Life (Chapters 1–3)
Difficulty: Easy · Biology I · Key topics: the scientific method, themes and properties of life, atoms and molecules, water’s unique properties, carbon chemistry, biological macromolecules (carbohydrates, lipids, proteins, nucleic acids)
Chapters in this block:
- 1. The Study of Life
- 2. The Chemical Foundation of Life
- 3. Biological Macromolecules
Unit I lays the chemical groundwork every later unit assumes without re-explaining. Chapter 1 opens with what makes something alive — the properties and themes shared across all organisms — and the scientific method itself, since biology is built on hypothesis testing and evidence, not assumption. Chapter 2 moves to chemistry: atomic structure, ions, and how atoms bond into molecules, spending particular attention on water, whose polarity, cohesion, and ability to moderate temperature make life as we know it possible, and on carbon’s unique ability to form the backbone of complex organic molecules. Chapter 3 builds those atoms into the four classes of biological macromolecules — carbohydrates, lipids, proteins, and nucleic acids — covering how monomers link into polymers through dehydration synthesis and how each macromolecule class’s structure enables its specific biological function, from enzymes to cell membranes to genetic storage.
Key Points:
- Living things share defining properties — organization, response to stimuli, reproduction, growth and development, regulation, homeostasis, energy processing, and evolutionary adaptation — and something must display essentially all of them to be considered alive
- The scientific method proceeds from observation to hypothesis to testable prediction to experiment, and a hypothesis is only useful if it can be falsified — a claim that cannot be tested or disproven isn’t scientific, however plausible it sounds
- Water’s polarity gives it cohesion, adhesion, a high specific heat, and the unusual property that ice floats — all four directly enable processes from capillary action in plants to temperature regulation in animals to aquatic life surviving winter
- Carbon can form four covalent bonds and link into chains, branches, and rings, which is why it (not silicon or any other element) is the structural backbone of every biological macromolecule
- Dehydration synthesis builds polymers from monomers by removing a water molecule at each bond, and hydrolysis breaks polymers back into monomers by adding water back in — the same two reactions, run in opposite directions, build and break every macromolecule class
- Carbohydrates store and supply energy and provide structural support (cellulose, chitin); lipids store energy long-term and form cell membranes; proteins do nearly all of a cell’s functional work (enzymes, transport, structure, signaling); nucleic acids store and transmit genetic information
- A protein’s function depends on its three-dimensional shape, which is determined by its amino acid sequence — denaturation (from heat, pH, or other stress) unfolds that shape and destroys function even though the amino acid sequence itself hasn’t changed
- pH measures hydrogen ion concentration on a logarithmic scale, and biological systems depend on buffers to resist pH swings, since even small pH changes can denature the proteins and enzymes a cell depends on
Practice Tip: Learn the four macromolecule classes as a table with three columns — monomer unit, polymer structure, primary biological role — rather than as separate isolated facts. Nearly every Chapter 3 exam question is really asking you to place a described molecule into the right row of that table.
Common Mistake: Assuming all four macromolecule classes are built and broken the same way chemically but serve interchangeable purposes. They are chemically similar (dehydration synthesis/hydrolysis applies to all four), but functionally distinct — using a lipid where the question is really asking about energy storage versus long-term energy storage, or confusing a protein’s structural role with an enzyme’s catalytic role, is the single most common Unit I mistake.
Important Questions:
- What is the difference between a hypothesis and a theory in the scientific method, and why does this distinction matter in biology? A hypothesis is a specific, testable proposed explanation for a single observation, while a theory is a broad, well-substantiated explanation supported by a large body of repeatedly tested evidence across many hypotheses — in everyday language “theory” sounds like a guess, but in science it is closer to the opposite: an explanation that has survived extensive, repeated testing. This distinction matters because dismissing a scientific theory (like evolution, covered in Unit IV) as “just a theory” misunderstands what the word means within the scientific method.
- Explain why water is described as a polar molecule, and name two biological consequences of that polarity. Water is polar because oxygen pulls shared electrons more strongly than hydrogen does, giving the oxygen end of the molecule a partial negative charge and the hydrogen ends a partial positive charge, creating an asymmetric charge distribution across the bent molecule. Two consequences: (1) hydrogen bonding between water molecules gives water high cohesion and surface tension, letting water move up a plant’s xylem and letting some insects walk on water’s surface; (2) water’s polarity makes it an excellent solvent for other polar and ionic substances, which is why so many biological reactions happen in an aqueous (water-based) environment inside cells.
Topic Block 2: The Cell (Chapters 4–10)
Difficulty: Medium · Biology I · Key topics: prokaryotic vs. eukaryotic cells, cell organelles, the endomembrane system, the cytoskeleton, cell-to-cell connections, plasma membrane structure, passive and active transport, bulk transport, metabolism and thermodynamics, ATP, enzymes, cellular respiration, photosynthesis, cell communication, the cell cycle and cell division
Chapters in this block:
- 4. Cell Structure
- 5. Structure and Function of Plasma Membranes
- 6. Metabolism
- 7. Cellular Respiration
- 8. Photosynthesis
- 9. Cell Communication
- 10. Cell Reproduction
Unit II is the largest unit in the book and covers everything the cell does as a living unit. It opens by comparing prokaryotic and eukaryotic cells and touring the eukaryotic organelles — nucleus, endomembrane system, mitochondria, chloroplasts, cytoskeleton — before moving to the plasma membrane itself: its fluid mosaic structure and the passive (diffusion, osmosis, facilitated diffusion) and active (pumps, endocytosis, exocytosis) mechanisms cells use to move material across it. Chapters 6–8 form the energy core of the unit: metabolism and thermodynamics establish why cells need a constant energy supply and how ATP and enzymes make reactions happen; cellular respiration then shows how cells extract that energy from glucose through glycolysis, the citric acid cycle, and oxidative phosphorylation; and photosynthesis shows how plants and other autotrophs capture light energy and store it as glucose in the first place — the two processes are near-mirror images of each other. The unit closes with how cells communicate with each other via signaling molecules and receptors, and how a cell reproduces itself through the cell cycle, mitosis, and its own tightly regulated checkpoints.
Key Points:
- Prokaryotic cells (bacteria, archaea) lack a membrane-bound nucleus and most organelles; eukaryotic cells (plants, animals, fungi, protists) compartmentalize their functions into membrane-bound organelles, which is the single most fundamental division in cell biology
- The plasma membrane’s fluid mosaic model describes a phospholipid bilayer studded with proteins that can drift laterally — hydrophilic phosphate heads face the watery environment on both sides while hydrophobic fatty acid tails face each other in the middle
- Passive transport (diffusion, facilitated diffusion, osmosis) moves substances down their concentration gradient and costs the cell no energy; active transport (pumps, endo/exocytosis) moves substances against their gradient and always requires energy, usually ATP
- Enzymes lower a reaction’s activation energy without being consumed themselves, and most are highly specific to one substrate because of their three-dimensional active site shape — this is why enzyme function is so sensitive to the denaturation discussed in Unit I
- Cellular respiration (glycolysis → citric acid cycle → oxidative phosphorylation) extracts energy from glucose and stores it as ATP, with oxidative phosphorylation (needing oxygen) producing far more ATP per glucose than glycolysis alone (fermentation) does without oxygen
- Photosynthesis’s light-dependent reactions capture light energy and produce ATP and NADPH, while the light-independent reactions (Calvin cycle) use that ATP and NADPH to build glucose from CO₂ — cellular respiration then runs this process essentially in reverse to release the stored energy
- Cell signaling follows a consistent three-step pattern — reception (a signaling molecule binds a receptor), transduction (the signal is relayed and amplified inside the cell), and response (the cell actually does something) — regardless of which specific molecules are involved
- The cell cycle (interphase → mitosis → cytokinesis) is controlled by checkpoints that verify DNA is undamaged and properly replicated before the cell is allowed to proceed — when these checkpoints fail, the result is uncontrolled division, which is the basis of cancer
Practice Tip: Draw cellular respiration and photosynthesis as mirror-image diagrams side by side, with respiration’s inputs (glucose + O₂) as photosynthesis’s outputs, and respiration’s outputs (CO₂ + H₂O) as photosynthesis’s inputs. Nearly every Chapters 7–8 exam question tests whether you understand this reciprocal relationship, not just the individual steps of either pathway.
Common Mistake: Assuming ATP is created or destroyed rather than continuously recycled, or confusing passive and active transport by direction alone. A cell doesn’t manufacture a large standing stock of ATP — it constantly regenerates ATP from ADP as fast as it’s used, which is why respiration must run continuously. And the deciding factor between passive and active transport is whether energy is spent, not simply which direction the substance moves — facilitated diffusion still moves down a gradient (passive) even though it requires a membrane protein to do so.
Important Questions:
- A plant cell is placed in a solution with a higher solute concentration than the cell’s cytoplasm (hypertonic). What happens to the cell, and why? Water moves out of the cell by osmosis, from the region of lower solute concentration (inside the cell) to higher solute concentration (the surrounding hypertonic solution), causing the cell to lose water and the plasma membrane to pull away from the cell wall — a process called plasmolysis. Osmosis is simply the diffusion of water across a selectively permeable membrane, always moving toward the side with more dissolved solute (and therefore less free water) until equilibrium is reached or, in this case, until the plant cell wall physically limits how far the membrane can shrink.
- Explain the overall relationship between the equations for cellular respiration and photosynthesis. Cellular respiration is essentially photosynthesis run in reverse: photosynthesis is 6CO₂ + 6H₂O + light energy → C₆H₁₂O₆ (glucose) + 6O₂, while cellular respiration is C₆H₁₂O₆ + 6O₂ → 6CO₂ + 6H₂O + ATP (usable energy). Photosynthesis captures light energy and stores it in glucose’s chemical bonds while releasing oxygen as a byproduct; respiration breaks those same bonds back down, consuming the oxygen and releasing the stored energy as ATP — together the two processes form the basic energy cycle connecting nearly all life on Earth.
Topic Block 3: Genetics (Chapters 11–17)
Difficulty: Medium–Hard · Biology I · Key topics: meiosis and sexual reproduction, Mendelian genetics and probability, chromosomal theory of inheritance, DNA structure and replication, DNA repair, transcription and translation, gene expression regulation, biotechnology and genomics
Chapters in this block:
- 11. Meiosis and Sexual Reproduction
- 12. Mendel’s Experiments and Heredity
- 13. Modern Understandings of Inheritance
- 14. DNA Structure and Function
- 15. Genes and Proteins
- 16. Gene Expression
- 17. Biotechnology and Genomics
Unit III traces inheritance from the cellular level down to the molecule and back up to modern biotechnology. It opens with meiosis, the specialized cell division that halves chromosome number to produce gametes and is the mechanical basis for sexual reproduction’s genetic variation. Chapter 12 covers Mendel’s pea-plant experiments and the probability laws (segregation, independent assortment) that still describe basic inheritance patterns today, while Chapter 13 extends those laws to the messier reality of chromosomal linkage, sex-linked traits, and chromosomal disorders that Mendel’s simple ratios don’t fully capture. Chapters 14–16 zoom into the molecule itself: DNA’s double-helix structure and semi-conservative replication, how genes are read out as proteins through transcription and translation (the central dogma), and how gene expression is regulated so that a cell with the same DNA as every other cell in the body can still specialize into wildly different cell types. The unit closes with Chapter 17’s biotechnology and genomics — the tools (PCR, gene cloning, CRISPR, whole-genome sequencing) that let scientists directly read, copy, and edit the genetic material this whole unit describes.
Key Points:
- Meiosis produces four genetically distinct haploid gametes from one diploid cell through two divisions (meiosis I and II), and crossing over plus independent assortment during meiosis I are the two mechanical sources of genetic variation in sexually reproducing species
- Mendel’s law of segregation states each organism carries two alleles per gene that separate during gamete formation, and the law of independent assortment states genes on different chromosomes are inherited independently of one another — both are direct consequences of how meiosis physically separates chromosomes
- A Punnett square predicts offspring genotype and phenotype ratios from a cross by treating each parent’s allele combination as equally likely to combine — a monohybrid cross gives the classic 3:1 phenotype ratio, and a dihybrid cross gives 9:3:3:1, assuming simple dominant/recessive inheritance and independent assortment
- DNA is a double helix of two antiparallel strands held together by hydrogen bonds between complementary base pairs (A-T, G-C), and replication is semi-conservative — each new double helix contains one original (parent) strand and one newly synthesized strand
- The central dogma of molecular biology — DNA is transcribed into mRNA, which is translated into protein — describes the one-directional flow of genetic information from gene to functional product in nearly all organisms
- The genetic code is read in three-nucleotide codons, is redundant (most amino acids are specified by more than one codon), and is nearly universal across all known life — a fact that is itself strong evidence for common ancestry, covered again in Unit IV
- Gene expression regulation — which genes a cell actually transcribes and translates, and how much — is what allows genetically identical cells to differentiate into radically different cell types (neuron, muscle, skin), and it operates at multiple levels: chromatin structure, transcription initiation, RNA processing, and post-translational modification
- Modern biotechnology tools (PCR to amplify DNA, restriction enzymes and gene cloning to isolate and copy genes, CRISPR-Cas9 to edit genes directly, whole-genome sequencing to read an organism’s entire genetic code) all depend directly on the DNA replication and transcription/translation mechanisms covered earlier in this unit
Practice Tip: Work through Punnett squares by hand for every practice cross rather than memorizing the standard ratios (3:1, 9:3:3:1) as fixed facts — exam questions frequently modify the standard case (incomplete dominance, codominance, sex-linkage, or a trihybrid cross) specifically to catch students who memorized ratios instead of the underlying method.
Common Mistake: Confusing DNA replication with transcription, or assuming dominant alleles are automatically more common or “better” than recessive ones. Replication copies DNA into more DNA (for cell division); transcription copies DNA into RNA (for protein synthesis) — mixing up which process happens when, and in which direction the genetic information moves, is the single most common error in this unit. And dominance is purely about which allele’s phenotype is expressed when both are present — it has no relationship to an allele’s frequency in a population or its evolutionary fitness.
Important Questions:
- A pea plant heterozygous for seed color (Yy, yellow dominant over green) is crossed with another heterozygous plant (Yy). What fraction of the offspring are expected to have green seeds? A Punnett square for Yy × Yy gives genotypes YY : Yy : Yy : yy, or a 1:2:1 ratio (1 YY, 2 Yy, 1 yy). Since yellow (Y) is dominant, only the yy offspring show the recessive green phenotype — that’s 1 out of 4, or 25% of offspring, expected to have green seeds, matching Mendel’s classic 3:1 dominant-to-recessive phenotype ratio.
- Describe the three main steps of the central dogma of molecular biology, and identify which step occurs in the cytoplasm in eukaryotic cells. The three steps are: (1) transcription, where an RNA polymerase copies a gene’s DNA sequence into a complementary mRNA molecule; (2) RNA processing, where the eukaryotic pre-mRNA is modified (splicing out introns, adding a cap and poly-A tail) into mature mRNA; and (3) translation, where a ribosome reads the mRNA’s codons and assembles the corresponding amino acid sequence into a protein. In eukaryotic cells, transcription and RNA processing happen inside the nucleus, while translation happens in the cytoplasm, at ribosomes either free-floating or attached to the endoplasmic reticulum — this physical separation is itself an extra layer of gene expression control unavailable to prokaryotes.
Topic Block 4: Evolutionary Processes (Chapters 18–20)
Difficulty: Medium · Biology II · Key topics: Darwin and evidence for evolution, natural selection, speciation and reproductive isolation, population genetics, the Hardy-Weinberg principle, adaptive evolution, phylogenetic trees and classification
Chapters in this block:
- 18. Evolution and the Origin of Species
- 19. The Evolution of Populations
- 20. Phylogenies and the History of Life
Unit IV is short in chapter count but is the conceptual foundation for every unit that follows it, since biological diversity, anatomy, and ecology all only make sense in an evolutionary context. Chapter 18 lays out the evidence for evolution (fossils, comparative anatomy, molecular biology, biogeography), Darwin’s mechanism of natural selection acting on heritable variation, and how new species form through reproductive isolation, whether geographic (allopatric) or otherwise (sympatric). Chapter 19 shifts from the individual organism to the population as the unit that actually evolves, introducing population genetics and the Hardy-Weinberg principle as the mathematical baseline for “no evolution happening,” against which real evolutionary forces — natural selection, genetic drift, gene flow, mutation — are measured as deviations. Chapter 20 closes the unit by showing how biologists reconstruct evolutionary relationships between species as phylogenetic trees, using shared derived characteristics and, increasingly, molecular/DNA evidence, and surveys the deep history of life from its earliest origins.
Key Points:
- Natural selection requires three conditions to operate: heritable variation must exist within a population, that variation must affect survival or reproduction, and the advantageous variants must be passed to offspring — remove any one condition and natural selection cannot act
- Evidence for evolution comes from multiple independent lines — the fossil record, comparative anatomy (homologous vs. analogous structures), molecular biology (DNA/protein sequence similarity), biogeography, and direct observation of evolution in fast-reproducing organisms like bacteria
- Speciation requires reproductive isolation — some barrier that prevents gene flow between diverging populations — and can be allopatric (a physical/geographic barrier) or sympatric (isolation without geographic separation, e.g. through polyploidy in plants or behavioral changes)
- The Hardy-Weinberg principle predicts allele and genotype frequencies will stay constant across generations only if five conditions hold: no mutation, no migration, infinite population size, random mating, and no natural selection — a real population almost always violates at least one, which is precisely how evolutionary change is detected and measured
- Genetic drift is random change in allele frequency, most powerful in small populations, and unlike natural selection it is not directional — a rare allele can become common (or vice versa) purely by chance, especially after a population bottleneck or founder event
- Adaptive evolution is natural selection specifically increasing the frequency of alleles that improve fitness in a given environment — it does not “aim” toward any goal or produce a “perfect” organism, only whatever variant reproduces most successfully in the current conditions
- A phylogenetic tree represents hypothesized evolutionary relationships, not proven fact, and is built primarily from shared derived characteristics (synapomorphies) — two species sharing a derived trait are inferred to share a more recent common ancestor than either shares with a species lacking that trait
- Homologous structures (same underlying anatomy, different function, due to shared ancestry — e.g. a human arm and a bat wing) are evidence for evolution, while analogous structures (similar function, different underlying anatomy, due to convergent evolution — e.g. a bird wing and an insect wing) are not, and confusing the two is a classic exam trap
Memory Tip: Remember Hardy-Weinberg’s five conditions with the acronym “No Real Fights In Mating” — No mutation, Random mating, no Flow (migration), Infinite population, no Mating selection (natural selection) — and remember that the equilibrium is a null hypothesis to test against, not a description of any real population you’ll actually encounter.
Common Mistake: Believing evolution acts on individuals or that it has a direction or goal (“evolving toward” something better). An individual organism cannot evolve during its own lifetime — only populations evolve, across generations, as allele frequencies shift. And natural selection has no foresight or purpose; it simply favors whatever variant currently reproduces more successfully, which is why a trait beneficial in one environment can become a liability the moment that environment changes.
Important Questions:
- In a population of 500 individuals, 84 are homozygous recessive (bb) for a trait. Using Hardy-Weinberg, estimate the frequency of the dominant allele B. First find q² (frequency of bb): 84/500 = 0.168. Then q = √0.168 ≈ 0.41 (frequency of the recessive allele b). Since p + q = 1, p (frequency of the dominant allele B) = 1 − 0.41 = 0.59. So the dominant allele B has an estimated frequency of about 59% in this population, assuming the population is in Hardy-Weinberg equilibrium.
- Distinguish between homologous and analogous structures, and give one example of each. Homologous structures share the same underlying anatomical origin because the species share a common ancestor, even if the structures now serve different functions — the bones in a human arm, a whale flipper, and a bat wing are homologous, all derived from the same ancestral forelimb pattern despite very different current uses. Analogous structures serve a similar function but arose independently through convergent evolution, not shared ancestry — a bird’s wing and a butterfly’s wing are analogous, since both fly but evolved flight through completely different anatomical starting points (a vertebrate limb versus an insect exoskeleton).
Topic Block 5: Biological Diversity (Chapters 21–29)
Difficulty: Medium · Biology II · Key topics: viral structure and classification, prokaryote diversity (bacteria and archaea), protists, fungi, seedless and seed plants, animal diversity and phylogeny, invertebrates, vertebrates
Chapters in this block:
- 21. Viruses
- 22. Prokaryotes: Bacteria and Archaea
- 23. Protists
- 24. Fungi
- 25. Seedless Plants
- 26. Seed Plants
- 27. Introduction to Animal Diversity
- 28. Invertebrates
- 29. Vertebrates
Unit V is the largest topic block in the book, surveying the full tree of life from the non-cellular (viruses) to complex vertebrates. Chapter 21 covers viruses — not classified as living organisms since they cannot reproduce independent of a host cell — their structure, classification, and how they infect hosts. Chapter 22 covers prokaryotic diversity: bacteria and archaea, their extraordinary metabolic diversity, and their roles as both pathogens and essential decomposers/nutrient recyclers. Chapters 23–24 cover protists (a polyphyletic grab-bag group not united by shared ancestry so much as by what they are not — not animal, plant, or fungus) and fungi (decomposers and symbionts, distinct from plants despite superficial similarity). Chapters 25–26 trace plant evolution from the first land plants through seedless plants (mosses, ferns) to the seed plants (gymnosperms, then angiosperms) that dominate most modern terrestrial ecosystems. Chapters 27–29 close the unit with animal diversity: the shared features that define animals, invertebrate phyla (the vast majority of animal diversity, from sponges to arthropods), and finally vertebrates, from fish through amphibians, reptiles, birds, and mammals.
Key Points:
- Viruses are not classified within any domain of life because they cannot reproduce or carry out metabolism on their own — they are obligate intracellular parasites that hijack a host cell’s own machinery to replicate, which is precisely why they are so hard to treat with drugs that don’t also harm the host cell
- Bacteria and archaea are both prokaryotic but are separate domains of life with distinct cell wall chemistry, membrane lipids, and genetics — archaea are often (though not exclusively) found in extreme environments and are, surprisingly, more closely related to eukaryotes than to bacteria in some respects
- Protists are defined more by exclusion than by shared ancestry — the group includes several separate evolutionary lineages united only by being eukaryotic and not fitting cleanly into the animal, plant, or fungus kingdoms, which is why modern classification increasingly abandons “Protista” as a single formal kingdom
- Fungi are more closely related to animals than to plants despite superficially plant-like immobility, and they digest food externally by secreting enzymes onto their surroundings and absorbing the resulting nutrients — the opposite strategy from an animal’s internal digestion
- Land plants evolved from a green algal ancestor and had to solve desiccation, structural support, and reproduction-without-water as they moved onto land — seedless plants (mosses, ferns) still require water for fertilization via swimming sperm, while seed plants (gymnosperms, angiosperms) evolved pollen and seeds specifically to reproduce without needing standing water
- Angiosperms (flowering plants) are the most diverse plant group today because of the evolutionary innovation of the flower and fruit, which recruit animals for pollination and seed dispersal — a coevolutionary relationship covered again in the Ecology unit
- Animals are defined by shared features including multicellularity, heterotrophy, lack of cell walls, and (in the vast majority) some form of nervous tissue and muscle tissue enabling movement — invertebrates (animals without a backbone) make up roughly 95% of all described animal species, far outnumbering vertebrates
- Vertebrate evolution shows a progression of adaptations for life on land — fish (fully aquatic) → amphibians (dual life, still tied to water for reproduction) → reptiles (amniotic egg frees reproduction from water) → birds and mammals (endothermy, among other traits) — though this is a simplified narrative, not a literal ladder, since each group continues evolving today
Memory Tip: Build a single evolutionary timeline across Chapters 21–29 rather than memorizing each group in isolation — viruses/prokaryotes, then protists, then the fungi/plant/animal split, then within animals the invertebrate-to-vertebrate progression. Nearly every exam question in this unit is really testing where a described organism sits on that timeline and why.
Common Mistake: Assuming evolutionary progression is linear or that “simpler” organisms are less evolved. Bacteria, protists, and invertebrates are not primitive stepping-stones on the way to “advanced” vertebrates — every currently living lineage, including bacteria, has been evolving for the same span of time since life began and is well adapted to its own niche. A phylogenetic tree branches; it does not have a single ladder-like main line with humans or vertebrates at the top.
Important Questions:
- Why are viruses not classified as living organisms, even though they have genetic material and can evolve? The standard definition of life requires independent metabolism and independent reproduction, and viruses have neither — they carry genetic material (DNA or RNA) but have no ribosomes, no metabolic machinery, and cannot replicate on their own; they must inject their genetic material into a host cell and hijack that cell’s ribosomes and enzymes to produce new virus particles. They do evolve (viral genetic material mutates and is subject to natural selection), which is why influenza and other viruses require new vaccines periodically, but evolving is not sufficient on its own to meet biology’s definition of a living organism.
- What key evolutionary innovation allowed seed plants to reproduce without standing water, unlike seedless plants such as ferns and mosses? Seed plants evolved pollen (which carries sperm cells inside a protective coat, transported by wind or animals rather than requiring the sperm to physically swim) and the seed itself (a protected, dormancy-capable embryo with its own stored food supply). Seedless plants like ferns and mosses still rely on free-swimming sperm that must travel through a film of water to reach an egg, which is why they remain restricted to moist habitats, while seed plants (gymnosperms and especially angiosperms) were freed to colonize drier terrestrial environments across the planet.
Topic Block 6: Plant Structure and Function (Chapters 30–32)
Difficulty: Medium · Biology II · Key topics: the plant body plan, stems, roots, leaves, water and solute transport (xylem and phloem), plant sensory systems and hormones, soil and plant nutrition, plant reproduction and pollination
Chapters in this block:
- 30. Plant Form and Physiology
- 31. Soil and Plant Nutrition
- 32. Plant Reproduction
Unit VI shifts from plant evolution (Unit V) to how a plant actually functions once it exists. Chapter 30 covers the plant body plan — the three main organs (roots, stems, leaves) and the tissue systems (dermal, vascular, ground) that run through all of them — and how water and dissolved nutrients move through a plant via xylem (driven largely by transpiration pulling water upward) and organic nutrients move via phloem (driven by pressure differences between sugar sources and sinks), closing with how plants sense and respond to their environment through hormones and tropisms. Chapter 31 covers plant nutrition specifically: which nutrients plants need, how soil composition and structure affect nutrient availability, and adaptations like nitrogen-fixing symbioses and carnivorous plants that solve nutrient shortages in unusual ways. Chapter 32 completes the unit with plant reproduction — the flower’s reproductive structures, pollination (often via animal coevolution, connecting back to Unit V’s angiosperm diversity), fertilization, and both sexual and asexual reproductive strategies.
Key Points:
- A plant’s body is organized into three tissue systems — dermal (the protective outer covering), vascular (xylem and phloem, for transport), and ground (everything else, mostly photosynthesis and storage) — that run continuously through all three organs: roots, stems, and leaves
- Xylem transports water and dissolved minerals upward from roots, driven primarily by transpiration (water evaporating from leaf stomata pulls a continuous water column upward through cohesion and adhesion) rather than by any pump the plant itself provides
- Phloem transports sugars and other organic nutrients from a “source” (typically photosynthesizing leaves, where sugar is produced) to a “sink” (roots, fruits, or growing tissue, where sugar is consumed or stored), driven by pressure differences rather than transpiration
- Stomata are microscopic pores on a leaf’s surface, controlled by paired guard cells, that open to allow CO₂ in for photosynthesis and inevitably let water vapor escape (transpiration) — balancing gas exchange against water loss is a constant tradeoff plants must manage, especially in dry conditions
- Plant hormones (auxins, gibberellins, cytokinins, abscisic acid, ethylene, among others) regulate growth and development, and tropisms (directional growth responses like phototropism toward light or gravitropism relative to gravity) are driven by hormones redistributing asymmetrically across a stem or root, not by the plant “choosing” a direction
- Plants require macronutrients (nitrogen, phosphorus, potassium, among others, needed in large quantities) and micronutrients (needed in trace amounts) from the soil, and soil structure and pH strongly affect how available those nutrients actually are to a plant’s roots regardless of how much is technically present
- Nitrogen-fixing bacteria (often in a mutualistic symbiosis with legume roots, forming root nodules) convert atmospheric nitrogen gas, which plants cannot use directly, into ammonia-based compounds plants can absorb — this symbiosis is why crop rotation with legumes improves soil fertility
- Flowering plant reproduction depends heavily on pollination, frequently by animals recruited through flower color, scent, and nectar rewards — a coevolutionary relationship between plant and pollinator that makes plant reproduction and the broader ecosystem’s animal populations directly interdependent, a theme picked up again in the Ecology unit
Practice Tip: Keep xylem and phloem straight with a simple rule: xylem only ever moves water and minerals upward from roots (one-way, driven by transpiration), while phloem moves sugars in whichever direction connects a source to a sink (which can be up or down the plant, depending on the season and which organs are actively photosynthesizing versus growing).
Common Mistake: Assuming a plant actively pumps water upward the way a heart pumps blood, or assuming all plant nutrients simply come “from the soil” without distinguishing availability from presence. Xylem transport is passive, driven by transpiration pulling from above and cohesion/adhesion holding the water column together — a plant has no pump. And a nutrient can be chemically present in soil yet biologically unavailable to roots because of pH, soil structure, or the absence of a symbiotic partner (like nitrogen-fixing bacteria) — “in the soil” and “available to the plant” are not the same thing.
Important Questions:
- Explain the cohesion-tension theory of water transport in xylem, and identify what actually powers the movement. The cohesion-tension theory explains that water evaporating from leaf stomata (transpiration) creates negative pressure (tension) at the top of the xylem column, and because water molecules cohere strongly to each other (via hydrogen bonding) and adhere to the xylem vessel walls, this tension pulls the entire continuous water column upward from the roots, against gravity, without requiring any active pump from the plant. The power source is ultimately the sun: solar energy evaporates water from the leaf surface, and that evaporation is what pulls the rest of the column up behind it.
- What is a nitrogen-fixing symbiosis, and why is it agriculturally significant? Certain bacteria (notably Rhizobium species) form a mutualistic symbiosis with legume plant roots, living inside root nodules where they convert atmospheric nitrogen gas (N₂), which plants cannot use directly, into ammonia-based compounds the plant can absorb and use to build amino acids and nucleic acids; in exchange, the plant supplies the bacteria with sugars from photosynthesis. This is agriculturally significant because nitrogen is usually the limiting nutrient for crop growth, and rotating nitrogen-fixing legume crops (like soybeans or clover) with nitrogen-demanding crops (like corn) naturally replenishes soil nitrogen without requiring as much synthetic fertilizer.
Topic Block 7: Animal Structure and Function (Chapters 33–43)
Difficulty: Hard · Biology II · Key topics: animal form and homeostasis, the digestive system and nutrition, the nervous system and neurons, sensory systems, the endocrine system, the musculoskeletal system, the respiratory system, the circulatory system, osmoregulation and excretion, the immune system, animal reproduction and development
Chapters in this block:
- 33. The Animal Body: Basic Form and Function
- 34. Animal Nutrition and the Digestive System
- 35. The Nervous System
- 36. Sensory Systems
- 37. The Endocrine System
- 38. The Musculoskeletal System
- 39. The Respiratory System
- 40. The Circulatory System
- 41. Osmotic Regulation and Excretion
- 42. The Immune System
- 43. Animal Reproduction and Development
Unit VII is the book’s largest topic block and works through every major animal organ system, with a recurring emphasis on human anatomy and physiology as the primary example. Chapter 33 introduces the unifying concept for the whole unit: homeostasis, the maintenance of a stable internal environment despite external change, achieved through negative feedback loops. From there the unit proceeds system by system — digestive (nutrient acquisition and processing), nervous and sensory (information processing and environmental detection), endocrine (chemical signaling via hormones, working alongside but more slowly than the nervous system), musculoskeletal (structural support and movement), respiratory (gas exchange), circulatory (transport of gases, nutrients, and wastes throughout the body), osmoregulatory/excretory (water and waste balance), immune (defense against pathogens), and finally reproductive and developmental biology (how a new organism is produced and built from a single fertilized cell). Every system in this unit exists to serve homeostasis, and the unit is best studied with that unifying thread kept explicitly in view rather than as eleven disconnected topics.
Key Points:
- Homeostasis — keeping internal conditions (temperature, pH, glucose, water balance, and more) within a narrow stable range despite a changing external environment — is maintained almost entirely through negative feedback loops, where a deviation from the set point triggers a response that pushes the system back toward that set point
- The digestive system breaks food down mechanically and chemically into absorbable nutrients, and different animal digestive strategies (monogastric, ruminant, avian gizzard-based) reflect adaptations to different diets, especially the difficulty of digesting cellulose in plant material
- The nervous system transmits information via electrical signals (action potentials) along neurons and chemical signals (neurotransmitters) across synapses, giving it a speed advantage over the endocrine system’s hormone-based signaling, which is slower but longer-lasting and better suited to sustained, body-wide regulation
- The endocrine system uses hormones traveling through the bloodstream to regulate body-wide processes on a slower timescale than the nervous system, and its major glands and their target organs form the backbone of Chapter 37, with special attention to feedback regulation of hormone levels (e.g. the hypothalamus-pituitary axis controlling many other glands)
- The respiratory and circulatory systems function as a coordinated pair — the respiratory system exchanges O₂ and CO₂ between air and blood at the alveoli, while the circulatory system’s heart and vessels then transport that oxygenated blood, along with nutrients, hormones, and waste products, throughout the entire body
- Osmoregulation and excretion (centered on the kidney and nephron in mammals) balance water and solute concentration in body fluids and remove nitrogenous waste (urea in mammals) — the kidney’s filtration-reabsorption-secretion process is one of the most detailed, exam-heavy topics in this entire unit
- The immune system has two coordinated layers: innate immunity (fast, non-specific, present from birth — barriers, inflammation, phagocytes) and adaptive immunity (slower to activate but highly specific and creates lasting memory — antibodies, T cells, B cells), and vaccination works specifically by priming the adaptive immune system’s memory response ahead of a real infection
- Animal development proceeds through a conserved general sequence — fertilization, cleavage, gastrulation (forming the three germ layers: ectoderm, mesoderm, endoderm), and organogenesis — and every organ in the body traces back to one (or a combination) of those three embryonic germ layers
Practice Tip: For each organ system chapter in this unit, explicitly write out its specific negative feedback loop (what is being sensed, what the set point is, and what response corrects a deviation) before memorizing anatomical structure names. Exam questions across Chapters 33–42 disproportionately test the feedback mechanism, not just organ or hormone names in isolation.
Common Mistake: Studying each organ system in total isolation rather than tracking how they interact, and confusing the nervous and endocrine systems’ relative speed and duration. The two are not competing systems but a coordinated pair: the nervous system typically triggers fast, short-term, precisely targeted responses, while the endocrine system typically produces slower-onset, longer-lasting, more diffuse body-wide responses — many real physiological responses (like the stress response) use both simultaneously, and treating them as interchangeable or purely separate is a common exam trap.
Important Questions:
- Explain how a negative feedback loop regulates human body temperature, using the components: stimulus, sensor, control center, and effector. The stimulus is a deviation in body temperature (e.g. it rises above the normal ~37°C set point); the sensor is thermoreceptors, largely in the hypothalamus and skin, that detect this deviation; the control center is the hypothalamus itself, which compares the sensed temperature to the set point; and the effectors are structures like sweat glands (increasing evaporative cooling) and blood vessels near the skin (dilating to release heat) that are activated to bring the temperature back down toward the set point. Once temperature returns to normal, the stimulus driving the response disappears, which is the defining feature of a negative feedback loop — the response counteracts, rather than reinforces, the original deviation.
- Distinguish between innate and adaptive immunity, and explain why vaccines specifically target the adaptive immune response. Innate immunity is the body’s fast, non-specific first line of defense — physical barriers like skin and mucous membranes, plus general responses like inflammation and phagocytic cells that attack any pathogen without needing to recognize it specifically, and it does not improve with repeated exposure. Adaptive immunity is slower to mount on first exposure but is highly specific to a particular pathogen (via antibodies and specialized T and B lymphocytes) and, critically, creates immunological memory, so a second exposure to the same pathogen triggers a much faster, stronger response. Vaccines work by safely exposing the immune system to a harmless version or component of a pathogen, which triggers the adaptive immune system to build that memory in advance, so that a real future infection is met with a rapid, already-primed adaptive response rather than starting from scratch.
Topic Block 8: Ecology (Chapters 44–47)
Difficulty: Medium · Biology II · Key topics: scope of ecology, biogeography and biomes, climate and global climate change, population demography and growth models, community ecology and species interactions, behavioral ecology, ecosystem energy flow and biogeochemical cycles, conservation biology and threats to biodiversity
Chapters in this block:
- 44. Ecology and the Biosphere
- 45. Population and Community Ecology
- 46. Ecosystems
- 47. Conservation Biology and Biodiversity
The final unit zooms all the way out from the individual organism (Unit VII) to how organisms interact with each other and their physical environment at every scale, and closes the entire book by returning to why biodiversity, covered across Units IV–VII, matters and is currently under threat. Chapter 44 defines ecology’s scope and covers biogeography (why species are distributed where they are), the world’s major terrestrial and aquatic biomes, and climate’s role in shaping them, including a direct treatment of global climate change. Chapter 45 moves to population ecology (demography, life history strategies, and the models — exponential and logistic growth — that describe how populations change size over time) and community ecology (species interactions like competition, predation, and symbiosis, plus behavioral ecology’s proximate and ultimate explanations for animal behavior). Chapter 46 covers ecosystem ecology: how energy flows one-directionally through trophic levels (with major loss at each transfer) and how matter, unlike energy, cycles repeatedly through biogeochemical cycles (carbon, nitrogen, water, phosphorus). The book’s final chapter, 47, closes with conservation biology — the current biodiversity crisis, why biodiversity matters to human life directly and indirectly, the main threats driving species loss, and strategies for preserving it.
Key Points:
- Ecology is studied at multiple nested scales — organism, population, community, ecosystem, biosphere — and a given ecological question (like “why did this species decline?”) often needs answering at more than one of these scales simultaneously
- Terrestrial biomes (like tropical rainforest, desert, tundra, and grassland) are defined primarily by climate — specifically temperature and precipitation patterns — rather than by which particular species happen to live there, which is why similar biomes on different continents can host completely different species with strikingly similar adaptations (a case of convergent evolution, from Unit IV)
- Exponential population growth (unrestricted, accelerating growth) is only realistic for a short time in a resource-unlimited environment; logistic growth, which levels off as a population approaches its environment’s carrying capacity (K), describes real population dynamics far more often, since resources are essentially always eventually limiting
- Species interactions are classified by their effect on each participant — competition (both harmed), predation and parasitism (one benefits, one harmed), and symbiosis in its various forms including mutualism (both benefit, e.g. the pollinator relationships from Unit VI) and commensalism (one benefits, one unaffected)
- Energy flows one-directionally through an ecosystem’s trophic levels (producers → primary consumers → secondary consumers, and so on) and roughly 90% is lost as heat at each transfer (the 10% rule), which is why food chains rarely extend beyond four or five trophic levels and why eating lower on the food chain supports far more total organisms per unit of primary production
- Unlike energy, matter is not lost from an ecosystem but cycles repeatedly through biogeochemical cycles — carbon, nitrogen (connecting directly back to Unit VI’s nitrogen-fixing symbiosis), phosphorus, and water — moving between living organisms, the atmosphere, oceans, and geological reservoirs on very different timescales for each element
- Behavioral ecology distinguishes proximate causes of a behavior (the immediate physiological or environmental trigger, e.g. a hormone level) from ultimate causes (the evolutionary reason the behavior increases fitness) — a complete explanation of any animal behavior typically needs both, not just one
- The current biodiversity crisis is driven primarily by habitat destruction, invasive species, overexploitation, pollution, and climate change, and Chapter 47 emphasizes biodiversity’s direct value (food, medicine, genetic resources) and indirect value (ecosystem services like pollination, water purification, and climate regulation) as the closing argument for why conservation matters, tying the entire book’s biological content back to a single practical stake
Memory Tip: Remember energy and matter move through ecosystems in fundamentally different ways — energy flows one-way and is progressively lost as heat at each trophic transfer (so it must be continuously resupplied by the sun via producers), while matter (carbon, nitrogen, water, phosphorus) cycles and is reused indefinitely. Confusing these two — treating energy as something that cycles back, or matter as something that gets “used up” — is the single most common Chapter 46 exam trap.
Common Mistake: Assuming an ecosystem’s carrying capacity is a fixed number or that population growth is normally exponential. Carrying capacity shifts with resource availability, climate, disease, and competition, and is a dynamic ceiling, not a constant; logistic growth (leveling off near carrying capacity) is the realistic long-term pattern for almost every natural population, with true unchecked exponential growth only occurring briefly, typically right after a population enters a new, resource-rich environment (an invasive species’ initial spread being a classic real-world example).
Important Questions:
- A population of 200 rabbits has a carrying capacity of 1,000 in its habitat and grows according to the logistic growth model. Qualitatively, how does its growth rate change as the population approaches 1,000, and why? Under the logistic growth model, the population’s growth rate is fastest when the population is at roughly half of carrying capacity (around 500 rabbits here) and slows progressively as the population approaches carrying capacity itself, approaching a growth rate of essentially zero as it nears 1,000. This happens because logistic growth incorporates a term, (1 − N/K), that shrinks toward zero as population size N approaches carrying capacity K, mathematically representing increasing resource competition, disease spread, and other density-dependent limiting factors that intensify as the population gets crowded, in contrast to unlimited exponential growth, which never slows down at all.
- Using the 10% rule of energy transfer, if a field of grass produces 10,000 kcal of energy through photosynthesis, roughly how much energy is available to a third-level consumer that eats a second-level consumer (which ate a first-level consumer, which ate the grass)? Applying the 10% rule at each of three trophic transfers: grass (producer, 10,000 kcal) → primary consumer receives about 10% = 1,000 kcal → secondary consumer receives about 10% of that = 100 kcal → tertiary consumer receives about 10% of that = 10 kcal. So roughly 10 kcal of the original 10,000 kcal of energy captured by the grass is actually available to the third-level consumer — illustrating why top predators are always far less numerous than the producers supporting the entire food chain beneath them, and why food chains rarely extend past four or five trophic levels.
Download Biology 2e PDF (Free)
This book is free from its official source, OpenStax. Click below to download the complete PDF — a free web-based reader edition (with per-section, linkable pages) is also available on the OpenStax site if you’d rather read online.
↓ Download PDFHow to Study This Book
This page groups Biology 2e’s 47 chapters into 8 topic blocks — one per the book’s own official Unit — rather than one block per chapter, since a chapter-by-chapter page at this length becomes unwieldy to scan. Every block still names its real chapter numbers and titles in full — nothing is hidden or summarized away, and the book itself is unchanged.
Units I–III (Chemistry of Life, The Cell, Genetics — topic blocks 1–3, Chapters 1–17) form Biology I at most institutions. Units IV–VIII (Evolutionary Processes, Biological Diversity, Plant Structure and Function, Animal Structure and Function, Ecology — topic blocks 4–8, Chapters 18–47) form Biology II. Check your own syllabus, since the exact split can vary by program.
Topic Block 2 (The Cell, Chapters 4–10) is the longest block in Biology I and the foundation for the rest of the book — cellular respiration and photosynthesis (Chapters 7–8) recur directly when Unit VI covers plant physiology and Unit VII covers animal metabolism, so treat this block as prerequisite knowledge, not a topic to revisit only before its own exam.
Topic Block 4 (Evolutionary Processes, Chapters 18–20) is short in chapter count but is the conceptual key to every unit that follows it — Unit V’s biological diversity, and even Unit VII’s animal anatomy, only make sense as products of evolutionary history. Do not treat it as a standalone topic to memorize and move past.
Topic Block 7 (Animal Structure and Function, Chapters 33–43) is the single largest block in the book at 11 chapters — budget the most study time here, and use homeostasis and negative feedback as the unifying thread across all eleven organ-system chapters rather than memorizing each system in isolation.
This is a two-semester, calculus-free text throughout, built for a Biology I & II sequence — basic chemistry (Unit I) is assumed as background, but no chemistry prerequisite course is required before starting this book.
Used In These Programs
This book is used for the two-semester Biology I & II course sequence in: BS Biology, Pre-Medical, Biochemistry, Environmental Science, and other STEM degree programs. Browse all Biology books or all Biology category books.
Who Should Read This
Biology 2e is written for a first- or second-year university student taking a two-semester introductory biology sequence — typically a BS Biology, Pre-Medical, Biochemistry, or Environmental Science student. Basic chemistry concepts (covered in the book’s own Unit I) are assumed, but no separate chemistry prerequisite course is required. Its extensive Visual Connection questions, chapter summaries, and Critical Thinking Questions suit a student who wants substantial self-check material alongside the core theory, and its consistent human-physiology emphasis in the later units suits Pre-Medical students specifically, not just Biology majors.
Applicable Universities
This book is useful for students at Pakistani universities offering BS Biology, Pre-Medical, Biochemistry, or Environmental Science programs with a two-semester introductory biology requirement, including Punjab University, Virtual University, COMSATS, FAST, UET, NUST, GIKI, and other HEC-recognized institutions, where a Biology I & II sequence is a common first- or second-year requirement.
FAQs
Is Biology 2e free?
Yes. OpenStax publishes it under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 (CC BY-NC-SA 4.0) licence, free to read online, download as a PDF, or print. OpenStax’s own required attribution line is simply “Access for free at openstax.org.”
Why are the 47 chapters grouped into 8 topic blocks on this page instead of one block per chapter?
Purely for readability — a 47-chapter, one-block-per-chapter page would be extremely long to scan. The 8 topic blocks match the book’s own official Unit divisions exactly (Unit I through Unit VIII), and every real chapter number and title is still listed in full inside its block. Nothing has been condensed, merged, or omitted from the actual textbook.
Does this book cover human anatomy and physiology in detail?
Yes, extensively — Unit VII (Animal Structure and Function, Chapters 33–43, Topic Block 7 on this page) covers the digestive, nervous, sensory, endocrine, musculoskeletal, respiratory, circulatory, excretory, immune, and reproductive systems, with human anatomy and physiology as the primary running example throughout.
Does this book cover one semester or two?
Two. Units I–III (Topic Blocks 1–3 on this page: Chemistry of Life, The Cell, Genetics, Chapters 1–17) typically form Biology I, and Units IV–VIII (Topic Blocks 4–8: Evolutionary Processes, Biological Diversity, Plant Structure and Function, Animal Structure and Function, Ecology, Chapters 18–47) typically form Biology II. Confirm the exact split against your own syllabus.
Is any chemistry background needed before starting this book?
Basic chemistry is covered inside the book itself, in Unit I (Chapter 2, The Chemical Foundation of Life), so no separate chemistry prerequisite course is strictly required. That said, students who have already taken introductory chemistry — such as this site’s Chemistry 2e — will move through Unit I faster.
Which edition is this, and is it still current?
The OpenStax 2nd edition (“2e”), published March 28, 2018. Core introductory-biology content — cell biology, genetics, evolution, anatomy and physiology, ecology — doesn’t date the way a rapidly changing applied field does, so this edition remains the standard, actively distributed OpenStax text.
Related Books
Biology 2e is this project’s first Biology-category book, covering a complete two-semester introductory biology sequence for BS Biology, Pre-Medical, Biochemistry, and Environmental Science students. Browse more Chemistry books or Physics books for the rest of your semester.
Biology 2e, by Mary Ann Clark, Jung Choi, Matthew Douglas, and contributors. OpenStax, Rice University. Free under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 licence. Access for free at https://openstax.org/details/books/biology-2e