L13 modern coexistence theory 1 Flashcards

1
Q

What is Modern Coexistence Theory?

A

A framework explaining how multiple species share environments by identifying mechanisms (e.g., niche differences) that stabilize coexistence.

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2
Q

How does Neutral Theory differ from Modern Coexistence Theory?

A

Neutral Theory assumes ecological equivalence—all species have identical birth, death, dispersal, and fecundity rates—so community dynamics are driven purely by stochastic drift.

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3
Q

What is a limiting resource?

A

A resource consumed by organisms whose depletion reduces others’ growth (e.g., soil water, nitrates for plants; prey for animals).

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4
Q

What does the Competitive Exclusion Principle state?

A

Two species sharing a single limiting resource cannot stably coexist if one species is strictly superior at depleting it.

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5
Q

In R* theory, which species wins competition?

A

The species that reduces the resource to the lowest equilibrium level while sustaining its population; the other species goes extinct.

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6
Q

What is niche differentiation?

A

Variation in ecological conditions (e.g., soil types, microhabitats) allowing species to specialize on different resources or conditions, avoiding direct competition.

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7
Q

How is each species’ niche defined?

A

By the range of conditions and resources under which it maintains positive population growth.

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8
Q

What are the Lotka–Volterra competition equations?

A

dN₁/dt = r₁N₁(1 – (N₁ + α₁₂N₂)/K₁), dN₂/dt = r₂N₂(1 – (N₂ + α₂₁N₁)/K₂).

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9
Q

What do competition coefficients (αᵢⱼ) represent?

A

The per-capita effect of species j on the growth of species i in the Lotka–Volterra model.

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10
Q

Under what condition do the Lotka–Volterra equations predict stable coexistence?

A

When intraspecific competition is stronger than interspecific competition (αᵢᵢ > αᵢⱼ for i≠j).

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11
Q

What is ecological equivalence in Neutral Theory?

A

The assumption that all species have identical demographic parameters (birth, death, dispersal, fecundity), so no species has a deterministic advantage.

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12
Q

What is recruitment limitation?

A

Limited dispersal and stochastic arrival of propagules (e.g., seeds, larvae) that prevent deterministic dominance and introduce demographic randomness.

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13
Q

Describe the zero-sum lottery model mechanics.

A

A fixed number of “sites” are always filled; when an adult dies, all survivors produce equal propagules, and one is drawn at random to fill the vacant site.

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14
Q

How does drift drive community dynamics in the neutral model?

A

With no deterministic growth differences, stochastic birth–death events (drift) cause random fluctuations in species abundances, leading to local extinctions and turnover.

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15
Q

What key concepts summarize the lecture’s core ideas?

A

1) Limiting resources & competitive exclusion; 2) Niche differentiation & competition coefficients; 3) Neutral Theory’s ecological equivalence & recruitment limitation; 4) Zero-sum lottery as a stochastic coexistence model.

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16
Q

In Hubbell’s neutral model, how is per capita growth related to species’ abundance?

A

Independent—higher death probability for common species is exactly offset by higher recruitment chances, so per capita growth is abundance-independent.

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17
Q

What does the logistic growth model describe?

A

Per capita growth rate: 1/N dN/dt = r(1 – N/K), where r is max per capita growth at low density and K is the carrying capacity.

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18
Q

What empirical evidence demonstrates density dependence?

A

Serengeti wildebeest data show per capita growth falls as population size rises, preventing unbounded growth.

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19
Q

How does neutral theory enforce community-level regulation?

A

By fixing the total number of “sites” (zero-sum), replacing species-specific K with a global constraint that caps total individuals.

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20
Q

Describe the illustrative neutral simulation setup and algorithm.

A

28 fixed sites, 3 species (7, 7, 14); for each of 800 events: randomly kill one individual, then refill the vacant site via an unbiased propagule lottery; repeat.

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21
Q

What key insight comes from varying simulation outcomes?

A

Only demographic stochasticity (drift) matters—runs differ wildly, with no deterministic pull toward coexistence or exclusion.

22
Q

Why does neutral drift eventually lead to monodominance?

A

Random birth–death fluctuations cause species extinctions until one remains; the winner is unpredictable, though large community size slows the process.

23
Q

How do speciation and immigration balance drift-driven extinctions?

A

New species arrivals (via speciation or dispersal) counteract random losses, and long adult lifespans slow turnover, sustaining diversity.

24
Q

What are Species Abundance Distributions (SADs)?

A

Patterns showing many rare and few common species, visualized as abundance histograms or rank–abundance plots (rank vs. log abundance).

25
Q

What is MacArthur’s broken stick model?

A

A neutral, purely mathematical model that randomly partitions a “stick” into abundance segments for species, lacking ecological processes.

26
Q

How did neutral theory reproduce observed SADs?

A

Hubbell’s model—using only stochastic birth, death, dispersal, and speciation—matched empirical SADs without species-specific parameters, suggesting randomness can drive macroecological patterns.

27
Q

What is the key flaw in pure Neutral Theory?

A

It assumes species are identical (fecundity, fitness, dispersal); even tiny fitness differences collapse the model.

28
Q

In the example simulation, what happens when one species’ fecundity is boosted from 1,000 to 1,500 seeds?

A

That species steadily outcompetes and excludes the others—deterministic advantage overrides drift.

29
Q

What are fitness differences?

A

Density-independent, constant advantages in per capita growth (e.g., higher fecundity or lower mortality) that don’t depend on other species’ abundances.

30
Q

What are niche differences?

A

Mechanisms causing intraspecific competition to exceed interspecific competition, generating negative frequency dependence that stabilizes coexistence.

31
Q

What does MacArthur’s warblers example illustrate?

A

Warbler species partition tree branches (resource partitioning), so each species limits itself more than others via niche differentiation.

32
Q

How do niche differences appear in Lotka–Volterra terms?

A

As αᵢᵢ > αᵢⱼ, meaning self-limitation exceeds interspecific effects.

33
Q

How is density-dependent fecundity incorporated into the neutral model?

A

Per capita fecundity fᵢ is made to decline as conspecific density Nᵢ increases, introducing a self-limiting term.

34
Q

In the modified fecundity function, what do fₘₐₓ and α represent?

A

fₘₐₓ is the maximum fecundity at low density; α is the strength of the stabilizing niche effect.

35
Q

What happens to species abundances when density-dependent fecundity is added?

A

All species persist with stochastic fluctuations bounded away from zero; rare species receive a fecundity “boost,” making extinctions rare.

36
Q

How does density-dependent fecundity create negative frequency dependence?

A

As a species becomes rare, its per capita fecundity rises steeply, increasing its chance to rebound.

37
Q

What is the effect of reintroducing a modest fitness advantage alongside niche effects?

A

The advantaged species is more abundant on average, but others still persist because niche stabilization counterbalances the advantage.

38
Q

When does niche stabilization fail to prevent exclusion?

A

If the fitness disparity is too large (e.g., fecundity boosted to 3,000), niche effects cannot offset the advantage, leading to exclusion.

39
Q

What balances species dynamics in the presence of both fitness and niche differences?

A

The trade-off between the magnitude of fitness differences and the strength of stabilizing niche effects.

40
Q

What are the two axes in Chesson’s coexistence framework?

A

Horizontal axis: fitness ratio (magnitude of density-independent differences); vertical axis: stabilization strength (niche, negative frequency dependence).

41
Q

What are equalizing mechanisms?

A

Processes that reduce fitness differences, moving species toward demographic equivalence (the neutral axis).

42
Q

What are stabilizing mechanisms?

A

Processes that increase niche differences, enhancing negative frequency dependence to stabilize coexistence.

43
Q

How is the coexistence region defined in the fitness–niche space?

A

It’s the “wedge” where stabilizing niche strength outweighs fitness differences, so both species can invade when rare.

44
Q

How is niche overlap ρ related to niche difference?

A

Niche difference = 1 – ρ; larger values mean stronger stabilizing effects.

45
Q

How is the fitness ratio defined?

A

As the ratio of species’ density-independent per capita growth parameters, indicating average competitive asymmetry.

46
Q

What is the invasion criterion for coexistence?

A

Each species must have a positive per capita growth rate when rare in the presence of the resident species.

47
Q

What does mutual invasibility mean?

A

Both species can invade each other’s equilibrium populations (both have positive invasion growth rates), ensuring stable coexistence.

48
Q

Why are stabilizing and equalizing mechanisms considered orthogonal?

A

They act on different components—stabilizing on frequency dependence (niche), equalizing on average growth rates (fitness).

49
Q

How can an annual‐plant model illustrate Chesson’s framework?

A

By deriving explicit expressions for niche overlap and fitness ratio from germination rates, seed production, and competition coefficients, then plotting them.

50
Q

Why is Chesson’s framework valuable?

A

It quantifies exactly how much niche partitioning and fitness parity are needed to sustain diversity, moving beyond simple neutral vs. niche debates.

51
Q

What do empirical studies need to estimate to apply Chesson’s framework?

A

Niche overlap (ρ) and fitness ratios for species pairs, then check if they fall within the coexistence region.