Principles of Ecology Week 5
Photo of Roseate Spoonbill by Joshua J. Cotten on Unsplash
Structured discussion about semester project
Groups of 3 people each, discussion for ~20 minutes.
Nominate a facilitator, a recorder, and a reporter
Each person to discuss:
What idea(s) did you have going into this project?
From your literature search, do you feel that your idea was too narrow/broad/just-right/other?
Among the primary literature (peer-reviewed articles in formal scientific journals), is there a good mix of “basic” ecology and “applied” environmental/social science?
What are some ways to connect material from class to your semester project?
What was one paper/idea/resource that surprised you from your search?
What are your next steps for (a) selecting a focal community from your options or (b) getting more information on the community you have selected?
Video of a Veery by Dan O’Brien on Macaulay Library
Whole-class discussion
The reporter should be prepared to share:
For each group member, what ecological community is (currently) the top candidate as the focus of the semester project?
For 1-2 group members, what are some challenges that you discussed that might make progress on this community difficult?
“The organism as the subject and object of evolution”
White pine trees in New England make such a dense shade that their own seedlings cannot grow up under them, so hardwoods come in and take their place.
On the other hand, organisms may make an environment more hospitable to themselves.
Grazing animals actually increase the rate of production of forage, both by fertilizing the ground with their droppings, and by stimulating plant growth by cropping.
Beavers create ponds by felling trees and building dams; indeed, a significant part of the landscape in northeastern United States has been created by beavers.
The takeaway is that the activity of any organism changes the environment in which it lives.
This can in turn shape the dynamics of other species.
Photo of the Everglades Basin from Getty Images
Brainstorm a list of ways in which species might interact with one another in this setting
Conceptual model of a pollination network from MacGregor et al. (2023), Ecological Entomology
Conceptual model of a plankton network in temperate from Merz et al. (2023), Nature Climate Change
Photo from Smithsonian’s Tropical Research Institute
e.g. In a forest that houses hundreds of tree species, how do two interact with each other?
In this class, we will explore both approaches…
Ecological communities as composites of pairwise interactions
Sp 1 effect on Sp 2 |
Sp 2 effect on Sp 1 |
Shorthand |
---|---|---|
Benefit (+) | Benefit (+) | |
Harm (–) | Harm (–) | |
Benefit (+) | Harm (–) |
Sp 1 effect on Sp 2 |
Sp 2 effect on Sp 1 |
Shorthand |
---|---|---|
Benefit (+) | Benefit (+) | Mutualism |
Harm (–) | Harm (–) | Competition |
Benefit (+) | Harm (–) | Predation |
Sp 1 effect on Sp 2 |
Sp 2 effect on Sp 1 |
Shorthand |
---|---|---|
Benefit (+) | Benefit (+) | Mutualism |
Harm (–) | Harm (–) | Competition |
Benefit (+) | Harm (–) | Predation Herbivory Parasitism |
Sp 1 effect on Sp 2 |
Sp 2 effect on Sp 1 |
Shorthand |
---|---|---|
Benefit (+) | Benefit (+) | Mutualism |
Harm (–) | Harm (–) | Competition |
Benefit (+) | Harm (–) | Predation Herbivory Parasitism |
Neutral (0) | Benefit (+) | Commensalism |
Neutral (0) | Harm (–) | Ammensalism |
To further complicate matters, the same pair of species can have different interactions under different conditions
Biological examples of mutualisms
Other examples?
Biological examples of competition
Competition can also be less overt – “apparent” competition
Unifying theme: one species benefits at the cost of the other . . .
One species benefits; the other is unaffected
e.g. Remora hitching a ride with a sea turtle
Sp 1 effect on Sp 2 |
Sp 2 effect on Sp 1 |
Shorthand |
---|---|---|
Benefit (+) | Benefit (+) | Mutualism |
Harm (–) | Harm (–) | Competition |
Benefit (+) | Harm (–) | Predation Herbivory Parasitism |
Neutral (0) | Benefit (+) | Commensalism |
Neutral (0) | Harm (–) | Ammensalism |
Why are we starting with this?
Key question: What effects can competition have on biodiversity patterns?
Relatively low species richness
Relatively high species richness, especially of native flowering plants
Given that species compete for shared resources, why do we observe more coexistence here…
… but less here?
Key question: What effects can competition have on biodiversity patterns?
Did we study any form of competition in the Population Ecology unit?
Competition is simply the reduction in fitness with higher densities of individuals
We learned about logistic growth as
\[\frac{dN}{dT} = rN\bigg(1-\frac{N}{K}\bigg)\]
But we can readily express it as \[\frac{dN}{dt} = rN(1-\alpha N)\]
where \(\alpha\) is \(\frac{1}{K}\)
When two species compete, the growth rate is also affected by the presence of a second (competing) species. How to account for this?
Given that intraspecific competition is modeled as
\[\frac{dN}{dt} = rN(1-\alpha N)\]
How to can extend this model to incorporate interspecific effects?
First, we need to account for the fact that there are two species: \(N_1\) and \(N_2\).
That means we have a system of equations: \(\frac{dN_1}{dt}\) and \(\frac{dN_2}{dt}\)
If species 1 is growing alone, its equation is:
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11} N_1)\]
If species 1 is growing alone, its equation is:
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11} N_1)\]
If species 2 is growing alone, its equation is:
\[\frac{dN_2}{dt} = r_2N_2(1-\alpha_{22} N_2)\]
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11} N_1) ~~~\text{ and} ~~~~ \frac{dN_2}{dt} = r_2N_2(1-\alpha_{22} N_2)\]
We can modify these to add the effects of the other species:
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11}N_1 - \alpha_{12}N_2)\]
\(\alpha_{11}\) is the competitive effect of species 1 on itself, \(\alpha_{12}\) is the competitive effect of species 2 on species 1, and \(N_i\) is the density of species \(i\)
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11}N_1 - \alpha_{12}N_2)\]
\[\frac{dN_2}{dt} = r_2N_2(1-\alpha_{21}N_1 - \alpha_{22}N_2)\]
How fast a population grows depends on
Consider what happens when a species is growing alone:
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11}N_1 - \alpha_{12}N_2)\]
Collapses down to logistic growth
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11}N_1)\]
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11}N_1 - \alpha_{12}N_2)\]
\[\frac{dN_2}{dt} = r_2N_2(1-\alpha_{21}N_1 - \alpha_{22}N_2)\]
The size of \(\alpha\) reflects “how competitive” interactions are:
Strong competition (high \(\alpha\)) happens when each additional individual of a species strongly reduces fitness of other individuals
In other words, \(\alpha_{12}\) are determined the degree to which an individual of species \(2\) changes the environment in a way that suppresses individuals of species \(1\)
Why are \(\alpha_{ii}\) and \(\alpha_{ij}\) different from one another?
When the species have highly overlapping niches, intra-specific and inter-specific \(\alpha\)s are very similar: \(\alpha_{ii} \approx \alpha_{ij}\)
When two species have highly distinct niches, intra-specific competition is very low: \(\alpha_{ij} \approx 0\)
\[\frac{dN_1}{dt} = r_1N_1(1-\alpha_{11}N_1 - \alpha_{12}N_2)\]
\[\frac{dN_2}{dt} = r_2N_2(1-\alpha_{21}N_1 - \alpha_{22}N_2)\]