L15 modern coexistence theory and community assembly Flashcards

1
Q

What is the focus of today’s lecture?

A

How Modern Coexistence Theory informs Community Assembly.

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2
Q

What does Modern Coexistence Theory (MCT) build on?

A

The idea that species’ interactions determine coexistence, assuming concepts like stabilizing vs. equalizing mechanisms.

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3
Q

What are the three main steps in the community assembly process?

A
  1. Regional Species Pool & Local Patches
  2. Environmental Filtering
  3. Formation of the Local Community
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4
Q

What is a Regional Species Pool & Local Patches?

A

A large pool of potential species and multiple smaller habitats each harboring a subset of those species.

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5
Q

What is Environmental Filtering?

A

Abiotic conditions acting as a filter—only species whose Fundamental Niche includes those conditions can pass.

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6
Q

How is a Local Community defined in community assembly?

A

The set of species (alpha diversity) present in a patch after abiotic filtering and biotic interactions.

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7
Q

Define Alpha Diversity.

A

Species richness within a local patch.

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8
Q

Define Beta Diversity.

A

Turnover or dissimilarity in species composition between patches.

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9
Q

Define Gamma Diversity.

A

Total species richness across the entire region (the full Regional Species Pool).

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10
Q

What is the Fundamental Niche?

A

The set of abiotic conditions under which a species can persist without biotic interactions.

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11
Q

What is the Realized Niche?

A

The subset of the Fundamental Niche after accounting for biotic interactions (competition, predation, etc.).

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12
Q

What role does Local Competition play in community assembly?

A

After passing the abiotic filter, species compete biotically; weaker competitors are excluded, narrowing the Realized Niche.

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13
Q

What is Dispersal Limitation?

A

Chance-based absence of species in patches due to limited arrival, even if conditions are suitable.

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14
Q

What are Priority Effects?

A

Historical sequence of colonization determining community outcomes when multiple stable states exist (e.g., Lotka–Volterra model scenarios).

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15
Q

How do Deterministic and Stochastic factors differ in community assembly?

A

Deterministic factors yield predictable outcomes from abiotic/biotic filters; stochastic factors involve chance and history (dispersal events, priority).

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16
Q

In the hypothetical tree community example, how would environmental filtering shape trait distributions?

A

Co-occurring species at each site should exhibit similar trait values matching local environmental conditions (phenotypic convergence).

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17
Q

What are the five most critical concepts summarized for community assembly?

A
  1. Environmental Filtering drives local establishment
  2. Realized Niches are narrower than Fundamental Niches
  3. Alpha, Beta, Gamma Diversity quantify local, between-site, and regional richness
  4. Dispersal Limitation & Priority Effects introduce stochasticity
  5. The balance of Deterministic vs. Stochastic processes is a central debate
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18
Q

Why move from species presence–absence to trait-based analysis in community assembly?

A

Traits are the direct targets of environmental and competitive filters, allowing clearer tests of assembly mechanisms.

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19
Q

What is Specific Leaf Area (SLA)?

A

The ratio of leaf area to dry mass; high SLA means thin, expansive leaves, low SLA means thick, dense leaves.

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20
Q

How does high SLA function ecologically?

A

It supports high light capture and growth rates where water is plentiful by fueling a strong transpiration stream.

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21
Q

What ecological advantage does low SLA confer?

A

Reduced water loss in arid or drought-prone environments.

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22
Q

What is the objective of null models and bootstrapping in trait analysis?

A

To determine if observed within-site trait distributions differ from random expectations.

23
Q

What is the procedure for trait-based null models?

A

Calculate observed trait statistic per site, randomly reassign species to sites many times, compute the statistic for each draw, and compare to the observed.

24
Q

What does trait clustering (observed variance < null variance) indicate?

A

Evidence of environmental filtering—co‐occurring species share similar traits.

25
Q

What does trait overdispersion (observed variance > null variance) indicate?

A

Evidence of niche differentiation—competition drives trait divergence.

26
Q

How was Kraft et al.’s Amazonian forest case study designed?

A

A 25 ha plot with ~150,000 mapped trees (~1,100 species), divided into 20×20 m quadrats; traits (e.g., SLA, seed mass, wood density) measured per species; species labels shuffled among trees to build null distributions.

27
Q

What did Kraft et al. find about SLA and topography?

A

SLA clustered by terrain: lower SLA on ridge tops and higher SLA in valleys, showing environmental filtering.

28
Q

How did Kraft et al. detect local competition via seed mass?

A

Within quadrats, observed seed mass variance exceeded null expectations, indicating overdispersion from competition.

29
Q

What ontogenetic shift did Kraft et al. observe?

A

Saplings’ trait distributions matched random expectation, while adults showed stronger trait structuring as competition thinned similar individuals.

30
Q

What is phylogenetic clustering and what does it imply?

A

Co‐occurring species are more closely related than expected, implying environmental filtering on conserved traits.

31
Q

What is phylogenetic overdispersion and what does it imply?

A

Co‐occurring species are more distantly related than expected, implying competition driving divergence in conserved traits.

32
Q

Why integrate abiotic, biotic, and evolutionary perspectives in community assembly?

A

Combining filters (abiotic/biotic) with phylogenetic context yields a richer, multiscale understanding of how communities form.

33
Q

Why incorporate phylogeny into community assembly analyses?

A

Phylogeny reveals evolutionary conservation of traits, helping infer whether filtering or competition drives community patterns.

34
Q

What was the design of the Florida oak community case study?

A

Seventeen oak species in Florida, grouped into red, white, and live oak clades; measured each species’ mean soil moisture preference and mapped them on a phylogeny.

35
Q

What pattern of soil moisture preference emerged among Florida oaks?

A

Closely related species often occupied contrasting moisture niches, showing phylogenetic overdispersion.

36
Q

What does phylogenetic overdispersion of a trait indicate?

A

Divergent adaptation within clades and niche partitioning driving diversification rather than conserved trait filtering.

37
Q

How was field co-occurrence analyzed in the oak study?

A

By calculating pairwise co-occurrence probabilities and comparing against phylogenetic distances among species.

38
Q

What did the oak co-occurrence analysis reveal within each clade?

A

Specialists on dry, intermediate, and wet niches evolved in each clade, and co-occurrence was higher among phylogenetically distant specialists.

39
Q

What is a key critique about defining the Regional Species Pool in trait studies?

A

Arbitrary spatial boundaries can bias results, making ‘regional pool’ delineations appear random.

40
Q

How does spatial scale sensitivity affect trait-based community assembly findings?

A

The size of sampling units (e.g., quadrat area) can change whether filtering or competition signals are detected.

41
Q

Why is separating environmental filtering from competition challenging?

A

Observed trait clustering may conflate abiotic filtering with competitive exclusion if both produce similar patterns.

42
Q

What limitation does experimental realism impose on trait-filter studies?

A

Only about 15% of studies properly isolate filtering and competition, making causal inference weak.

43
Q

How does Modern Coexistence Theory (MCT) refine classical trait-pattern predictions?

A

By partitioning coexistence into niche differences (stabilizing) and fitness differences (equalizing), tailoring expectations per trait.

44
Q

Under MCT, what pattern is expected for traits linked to fitness differences?

A

Phenotypic convergence (clustering) reduces fitness disparities and promotes coexistence.

45
Q

Under MCT, what pattern is expected for traits linked to niche differences?

A

Phenotypic overdispersion (divergence) maximizes niche separation and promotes coexistence.

46
Q

How do classical vs. MCT perspectives differ on interpreting competition signals?

A

Classical: competition always yields overdispersion; MCT: competition may yield clustering for fitness traits and overdispersion for niche traits.

47
Q

Describe the algal competition experiment using MCT.

A

Monoculture growth assays for fitness, mutual invasion trials for invasibility, across 8 freshwater green algae species.

48
Q

Which MCT metrics predicted coexistence in the algal experiment?

A

Niche differences (invasion-rate divergence) predicted coexistence; fitness differences did not.

49
Q

What was the phylogenetic signal outcome in the algal MCT study?

A

No phylogenetic signal for coexistence, niche, or fitness differences—key traits were evolutionarily labile.

50
Q

Why is classical trait-clustering vs. overdispersion theory considered overly simplistic?

A

It ignores trait-specific roles in fitness vs. niche axes and evolutionary lability, leading to mixed or misleading signals.

51
Q

What outstanding challenges remain for community assembly research?

A

Defining regional pools and scales, linking field trait patterns to coexistence mechanisms, and integrating variable phylogenetic signals.

52
Q

How does trait phylogenetic signal affect assembly predictions?

A

Conserved traits yield clear clustering/overdispersion interpretations, while labile traits weaken phylogenetic inference.

53
Q

Why must co-occurrence analyses account for clade-level niche partitioning?

A

Because closely related species may diverge ecologically within clades, masking true filtering or competition drivers.