HomeBiology › Q
BiologyEcology
The logistic growth equation for a population is best represented as:
Options
1
$\dfrac{dN}{dt} = rN$
2
$\dfrac{dN}{dt} = rN\left(\dfrac{K-N}{K}\right)$
3
$N_t = N_0 e^{rt}$
4
$\dfrac{dN}{dt} = rN\left(\dfrac{N-K}{K}\right)$
Correct Answer
$\dfrac{dN}{dt} = rN\left(\dfrac{K-N}{K}\right)$
Solution
1

Logistic growth = S-shaped (sigmoid) curve. Growth limited by carrying capacity K.

A: dN/dt = rN = exponential growth (no limit) ✗

C: Nt = N0e^rt = integrated exponential ✗

2

B: $\dfrac{dN}{dt} = rN\left(\dfrac{K-N}{K}\right)$ = correct logistic equation ✓

D: Wrong sign (N-K)/K ✗

Answer: B

Logistic growth: $dN/dt = rN(K-N)/K$
K = carrying capacity, S-shaped sigmoid curve
Theory: Ecology
1. Population Growth Models

Exponential (Malthusian) growth: dN/dt = rN. N = population size. r = intrinsic rate of natural increase (births - deaths per individual per time). Integrated form: Nt = N0 e^rt (continuous) or Nt = N0 lambda^t (discrete, lambda = finite rate of increase). J-shaped curve. No resource limitation. Occurs when: resources unlimited, no predators/competitors, new colonisation. Examples: bacteria in ideal conditions, introduced species in new habitat, human population historically. Logistic growth (Verhulst, 1838): dN/dt = rN[(K-N)/K]. K = carrying capacity = max sustainable population. (K-N)/K = unutilised reproductive capacity. When N << K: growth nearly exponential. When N = K/2: growth rate maximum (inflection point of S-curve). When N = K: dN/dt = 0. S-shaped (sigmoid) curve. Real populations rarely perfectly logistic but useful model.

2. Carrying Capacity and Limiting Factors

Carrying capacity (K): determined by available resources (food, water, space, nesting sites, light for plants). Density-dependent factors: intensity increases as population density increases. Competition, predation, disease, parasitism, food shortage. Regulate populations around K. Negative feedback. Density-independent factors: affect population regardless of density. Weather events, natural disasters, temperature extremes. Can cause sudden population crashes. Intraspecific competition: between individuals of same species. Strongest type of competition (same niche). Interspecific competition: between different species. May lead to competitive exclusion or niche differentiation. Predator-prey cycles: Lotka-Volterra equations describe oscillating predator-prey dynamics. Lynx-snowshoe hare cycles (Canada, ~10 year cycles). Evidence for both density-dependent and density-independent regulation.

3. Life Tables and Population Parameters

Life table: age-specific survival and fecundity data. Cohort (horizontal) life table: follows group of same-age individuals from birth to death. Static (vertical) life table: age structure at one time point. Parameters: lx = survivorship (fraction surviving to age x). mx = fecundity at age x (female offspring per female). Net reproductive rate R0 = sum(lx*mx). R0 > 1: population growing. R0 = 1: stable. R0 < 1: declining. Generation time T = sum(x*lx*mx)/R0. Intrinsic rate of increase r = ln(R0)/T (approximately). Survivorship curves: Type I: low juvenile mortality, most die old (humans, elephants, K-strategists). Type II: constant mortality at all ages (birds, many lizards). Type III: high juvenile mortality, survivors live long (oysters, fish, r-strategists). Population age structure: growing population: many young (triangular pyramid). Stable: even distribution. Declining: few young.

4. Interspecific Interactions

Competition (-/-): both species harmed. Competitive exclusion principle (Gause): two species competing for identical resources cannot coexist. One will outcompete and eliminate the other. Character displacement: competing species diverge in resource use when sympatric. Beak size divergence in Galapagos finches. Predation (+/-): predator benefits, prey harmed. Predator adaptations: speed, camouflage, venom, cooperative hunting. Prey adaptations: speed, armor, spines, warning coloration, mimicry, schooling behaviour. Herbivory: plant (+/-): secondary metabolites (alkaloids, tannins, terpenes) as defence. Mutualism (+/+): both benefit. Mycorrhizae: fungus provides minerals, plant provides sugar. Nitrogen-fixation: Rhizobium provides fixed nitrogen to legumes, gets carbon. Cleaner fish: removes parasites from larger fish (both benefit). Commensalism (+/0): one benefits, other unaffected. Epiphytes (orchids on trees: use tree for support, tree unaffected). Amensalism (-/0): one harmed, other unaffected. Antibiotic production by bacteria kills nearby bacteria.

5. Population Regulation

Top-down regulation (trophic cascade): predators regulate prey populations, which in turn regulate lower trophic levels. Removal of wolves from Yellowstone: elk populations exploded, overgrazing devastated riparian vegetation, which altered river courses, reduced beaver populations. Wolf reintroduction reversed effects (1995). Bottom-up regulation: resource availability controls producer populations, which cascade upward through food web. Nutrient addition (eutrophication) increases algal growth, algae supports more herbivores, etc. Regulation usually involves both mechanisms. r vs K selection (MacArthur and Wilson): r-selected species: short lifespan, many small offspring, little parental care, boom-bust populations, colonisers. K-selected species: long lifespan, few large offspring, extensive parental care, stable populations near K. Continuum not a strict dichotomy.

6. Biodiversity and Ecosystem Stability

Species richness: number of species in an area. Species diversity: richness + evenness (relative abundance). Shannon index H = -sum(pi * ln pi). Simpson's index D = 1 - sum(pi^2). Diversity-stability relationship: more diverse communities are generally more stable (resilient and resistant). Insurance hypothesis: more species = more functional redundancy = community can withstand species losses without losing function. Portfolio effect: diverse portfolio of species with different responses to environmental variability leads to stable overall community function (like diversified investment portfolio). Keystone species: disproportionately large impact on ecosystem relative to their abundance. Sea otter, wolf, fig tree (provides food and habitat for many species). Removal = ecosystem collapse. Foundation species: create and maintain habitat structures. Kelp forests (support hundreds of species), beaver dams (create wetlands). Ecosystem engineers: modify physical environment creating habitats.

7. Ecological Pyramids

Ecological pyramids: graphical representation of trophic levels. Pyramid of numbers: number of individuals at each trophic level. Usually decreases upward. Inverted in parasitic food chain (one large tree supports many insects, many insects support more parasites). Pyramid of biomass: total dry weight of organisms at each trophic level. Usually decreases upward. Can be inverted in aquatic ecosystems (phytoplankton biomass less than zooplankton at any one time due to rapid turnover). Pyramid of energy: always upright. 10% energy transfer between trophic levels. Never inverted. Most fundamental representation of ecosystem function. Energy is always lost as heat at each trophic level (respiration). Global energy flow: solar energy captured by photosynthesis = ~1-2% efficiency. GPP of terrestrial ecosystems: ~120 Gt C/year. GPP of oceans: ~50-55 Gt C/year. Human appropriation of NPP (HANPP): ~25-40% of all terrestrial NPP.

8. Global Environmental Issues

Global warming and climate change: CO2 from fossil fuels + deforestation. Methane from cattle, rice paddies, landfills. Nitrous oxide from fertilisers. Greenhouse effect traps heat. IPCC: 1.1°C warming above pre-industrial already occurred. 1.5°C expected by 2030s. Consequences: sea level rise (melting glaciers + thermal expansion), extreme weather events, species range shifts, coral bleaching, food security threats. Ozone depletion: CFC (chlorofluorocarbon) from aerosols, refrigerants. Cl atoms catalytically destroy ozone in stratosphere. Antarctic ozone hole seasonal. UV-B increases: skin cancer, cataracts, damage to phytoplankton. Montreal Protocol (1987): international ban on CFCs. Ozone layer slowly recovering. Acid rain: SO2 and NOx from burning fossil fuels + water = H2SO4, HNO3. pH below 5.6. Destroys forests, acidifies lakes, corrodes buildings. Eutrophication: nutrient pollution (nitrogen, phosphorus from agriculture, sewage) causes algal blooms, oxygen depletion, fish kills.

Frequently Asked Questions
1. What is the significance of the logistic growth equation in ecology?
The logistic equation (Verhulst, 1838) is one of ecology's most important mathematical models. Key insights: (1) Density-dependent growth: as population grows, per capita growth rate decreases due to resource depletion and competition. (2) Carrying capacity concept: formalizes the idea that environments have finite resource limits. (3) Stable equilibrium: populations self-regulate toward K (negative feedback). Population above K declines; below K grows. (4) Maximum sustainable yield: population grows fastest at N = K/2 (inflection point). This is the theoretical basis for sustainable harvesting of fish/wildlife populations. (5) Predicts S-shaped population growth observed in many real populations (yeast in flask, sheep on Tasmania). Limitations: real populations often overshoot K then decline; K not constant; interactions not captured; spatial variation ignored. Extensions: Lotka-Volterra competition, predator-prey equations, age-structured models.
2. What is the difference between r and K selection strategies?
r-selection: adapted to unstable, unpredictable environments. r = intrinsic rate of increase (maximised). Many small offspring quickly, little parental investment, short generation time. Examples: bacteria, insects, annual plants, small mammals (rats). Boom-bust population dynamics. K-selection: adapted to stable, predictable environments near carrying capacity K. Few large offspring, much parental investment, long generation time. Examples: elephants, whales, oak trees, humans, large raptors. Stable populations near K. Intermediate organisms show a continuum. MacArthur and Wilson (1967): islands near mainland (recolonised frequently) favour r-selection; remote islands (rare colonisation) favour K-selection. r-K spectrum now viewed as one dimension of a broader "fast-slow" life history continuum. Fast-slow continuum: fast = early maturity, many offspring, short lifespan. Slow = late maturity, few offspring, long lifespan. Applies to organisms within groups not just across taxa.
3. Explain what happens when N exceeds K in the logistic model?
In the logistic equation dN/dt = rN(K-N)/K: when N > K, the term (K-N) becomes negative, so (K-N)/K is negative. Therefore dN/dt is negative (assuming r > 0). The population declines back toward K. This represents negative feedback regulation: overshoot of carrying capacity → resource depletion → increased mortality/decreased reproduction → population decreases → resources recover → population stabilises at K. In reality, populations often overshoot K and oscillate around it before settling. The oscillation can be damped (stable spiral) or persistent (limit cycles) depending on parameters like r (higher r → more oscillation). In extreme cases with very high r: chaotic dynamics possible. Example: a population introduced to new island with unlimited food initially grows exponentially, then overshoots K as food depletes, may crash back to low numbers, then stabilises at K or oscillates.
4. What is the difference between GPP, NPP and secondary productivity?
GPP (Gross Primary Productivity): total rate of photosynthesis = total organic matter produced by autotrophs per unit area per unit time. Units: g C m-2 yr-1 or kcal m-2 yr-1. Includes all energy fixed even if immediately used for plant respiration. NPP (Net Primary Productivity): GPP minus plant respiration = organic matter available to consumers. NPP = GPP - R (autotroph respiration). Typically NPP ≈ 40-60% of GPP. For terrestrial tropical forests: GPP ~2000-3000 g C m-2 yr-1, NPP ~1000-1500 g C m-2 yr-1. Secondary productivity: rate of organic matter production by heterotrophs (consumers). At each trophic level: ~10% of energy from previous level incorporated into biomass (Lindeman efficiency). Rest lost as heat (respiration), excretion, undigested food. Net Secondary Productivity = Assimilation - Respiration. Always much less than NPP. This is why herbivores outnumber carnivores and food chains rarely exceed 4-5 trophic levels.
5. What is the Competitive Exclusion Principle and when does coexistence occur?
Competitive Exclusion Principle (Gause, 1934): two species competing for identical resources in the same habitat cannot coexist indefinitely. One will outcompete and eliminate the other (or drive it to local extinction). Evidence: Paramecium aurelia and P. caudatum in lab culture with same food source - P. aurelia always wins. Conditions for coexistence despite competition: (1) Niche differentiation: species use slightly different resources or differ in microhabitat use. (2) Frequency-dependent selection: common species at competitive disadvantage. (3) Predator-mediated coexistence: predator preferentially eats dominant competitor, allowing weaker competitor to persist (Janzen-Connell effect in tropical forests). (4) Fluctuating environments: competitive advantage shifts between species as conditions change (storage effect). (5) Spatial/temporal heterogeneity: different species dominate in different patches. Stable coexistence requires some mechanism of niche separation.
Previous Questions
Q.
Basic amino acids Lysine Arginine Histidine positively charged side chains pH 7.4
Biology . Lysine and Arginine
Q.
Ectoparasite Pediculus humanus head louse on surface of host body
Biology . Pediculus humanus
Q.
Convergent evolution analogous organs unrelated organisms similar environment
Biology . Convergent evolution
Q.
Meselson Stahl semi-conservative replication 15N 14N Statement I correct II incorrect
Biology . I correct II incorrect
Q.
George Gamow proposed triplet genetic code 4 cubed 64 codons 20 amino acids
Biology . George Gamow