Community Ecology
Food webs & top-down vs. bottom-up controls

Outline:

1. History of the food web concept

A. Elton’s pyramid of numbers

B. Lindeman’s estimates of ecological efficiency

2. Structure, composition, and properties of food webs

A. Structure: nodes and links

B. Composition: basal, intermediate, and top predator species

C. Properties

i. cycles are rare

ii. link-scaling law: linkage density constant across webs

iii. connectance decreases as richness increases

a. implication: food web connectance is inversely related to system stability diversity/stability debate

iv. food chains are short

v. food chains are shorter in 2D than in 3D habitats

vi. greater environmental constancy leads to greater web connectance

3. Do predators regulate prey or vice versa?

A. HSS - an explanation for "why the world is green"

i. criticisms - Murdoch, Ehrlich and Birch

ii. reply - SSH

iii. what about aquatic systems? Wiegert and Owen

a. Fretwell - alternation of regulatory mechanisms

b. Hairston and Hairston - number of terrestrial vs. aquatic trophic levels

c. Oksanen - influence of primary productivity

4. Top-down vs. bottom-up regulation

Terms/people:

food web (cf. food chain) Chas. Elton node

link Oksanen Murdoch

"why the world is green" (HSS)energetic constraint hypothesis

trophic cascade (trickle?) ecological efficiency pyramid of numbers

R. Lindeman Hairston, Smith, Slobodkin (HSS)

Wiegert and Owen Fretwell donor control

top-down regulation bottom-up regulation Stuart Pimm

compartment (subweb) connectance link-scaling

linkage density interval Joel Cohen

Ehrlich and Birch

Food web: (see Fig.s 10.1-10.4 in Mittelbach text)

cf. food chain

A food web is the pattern of flows of energy and material among organisms that result when some organisms eat other living organisms or their parts. Food webs provide a pattern of basic ecological interactions among species and trophic levels. Food webs describe a pattern of ecological relationships but do not in themselves provide evidence of ecological processes. Food webs are useful as descriptions of ecological systems. They have been much-studied in community ecology.

Charles Elton (1927, Animal Ecology)

"pyramid of numbers" (a.k.a. Eltonian pyramid)
But how do we explain the inverted pyramid seen in aquatic systems?

Lindeman (1942) - ecological efficiency limits to chain length

Structure of a food web: nodes and links

Composition: basal spp. (producers), intermediate spp. (herbivores, lower predators), top predators

Properties of food webs (Pimm 1982, Lawton and Warren 1988, Cohen et al. 1989): empirical evidence limited and mechanisms unclear for many of these! But most are related to ecological efficiency.
1) cycles (loops) are rare
2) link-scaling law: linkage density is constant across webs
3) connectance (ratio of actual interactions: possible interactions in a food web) decreases as species richness increases
c=L/{[S(S-1)]/2}
where c=connectance, L=observed number of links, S=number of nodes (if S spp., then S-1 links are possible)
0 c 1
Implications: food web connectance is inversely related to system stability

Species richness / stability debate
4) food chains are short due to energetic constraint hypothesis(Jenkins et al. 1992)
5) food chains are shorter in physiognomically simpler environments
6) effects of environmental variation

BUT...these properties/patterns were based on:
- mostly studies on vertebrates
- mostly simple webs (since they are easier to study, easier to observe connections): "artistic convenience" (e.g. Paine’s keystone system of 7 nodes represented a community of over 300 species!)

And keep in mind: food webs can and do change over time.

Do predators regulate prey or vice versa?

bottom-up food web regulation vs. top-down food web regulation

Hairston, Smith, Slobodkin 1960 (HSS 1960) - "why the world is green" generated controversy

criticisms - Murdoch (1966), Ehrlich and Birch (1967): idea is untestable, world may be green but is not entirely edible

reply - SSH (1967)

What about aquatic systems? They don't appear to be green (Wiegert and Owen 1971)

explanations for differences between terrestrial and aquatic systems:

Fretwell (1977) - alternation of regulatory mechanisms; Hairston and Hairston (1993) applied this to terrestrial vs. aquatic trophic levels (different numbers of trophic levels)

And another thing: "it makes no sense to ask why the world is green while standing in the middle of the Atacama desert or the northern shores of Greenland" (Oksanen 1988), i.e., effects of predators or competitors varies along a gradient of primary productivity. In unproductive habitats herbivores are rare because there is not enough forage to support them. At the highest productivity there will only be few herbivores because herbivores are limited by predators. At intermediate productivity, plants are limited by herbivores because there insufficient herbivores to support large numbers of predators. Consequently, plants should compete in the least and the most productive ecosystems. The most productive systems are green but would not be so if predators were removed. Herbivores compete in ecosystems of intermediate productivity, and predators compete in ecosystems of highest productivity. Evidence to support the Oksanen model:

  1. Relationship between biomass and productivity matches model predictions.
  2. Herbivore removal experiments almost always lead to increases in plants.
  3. Predictions of the model have been confirmed in experimental studies: Plants should compete in habitats of low or high productivity only. Thirty-one plant competition experiments in green worlds (forests, meadows) clearly demonstrated competition; 6 did not. In intermediate productivity ecosystems (grasslands, arid areas), 4 demonstrated competition, 25 did not. In low productivity systems (deserts), 4 demonstrated competition and none failed to do so.

Ultimately, all food webs depend on producers: therefore, "plants have primacy" (Power 1992)  called donor control (Strong 1992)

Bottom-up (donor control) -

-Organisms on each trophic level are limited by the resources available from the level below.

-Logically, plants have primacy in biotic systems because a system that lacks primary producers lacks resources for consumers to comprise a trophic structure

-But, given sufficient resources to support a community, the relative effects of resources and consumers should be critical in understanding the processes that structure communities.

-Bottom up forces include level of primary productivity and availability of light or nutrients.

Top-down (trophic cascade) -

-Top-down forces include predation and herbivory.

-are more like "trophic trickles" than cascades (Strong 1992), especially in speciose communities because the "trophic tangle precludes cascades"

-Successive trophic levels alternate between consumer limitation and resource limitation.

-Primary produces will be resource limited in chains that contain odd numbers of trophic levels (i.e., predators reduce herbivores[and herbivory] in a three-trophic level community)

-Primary producers will be consumer limited (i.e., competition among consumers) in habitats that contain an even number of trophic levels.

-Terrestrially, trophic cascades with top-down dominance are restricted to systems of low species diversity.

-But in many places, predators have been extirpated (Terborgh et al. 2001 call this an “ecological meltdown”).

-The number of trophic levels may be constrained by the level of primary productivity in a community.

-Oksanen et al. (1981) formalized this idea by arguing that effective top-down forces are only likely to occur in habitats with high primary productivity, since low productivity habitats do not have functional upper trophic levels.

There is no clear pattern with respect to the kinds of terrestrial systems likely to exhibit top-down or bottom-up trophic cascades. Instead, they are scale-dependent (Gripenberg and Roslin 2007).

Something to think about: recall the lecture on the importance of biodiversity to community health/stability. After learning about food webs today, is biodiversity a good assay of community health or stability?

For MUCH more information on the complex topic of food webs, check out But be prepared: Even Robert May (1999) called this “Heady stuff, verging on the Newtonian.”

Next time: scale

References:

Berryman, A.A. 1993. Food web connectance and feedback dominance, or does everything really depend on everything else? Oikos 68:183-185.

Briand, F., and J.E. Cohen. 1987. Environmental correlates of food chain length. Science 238:956-960.

Cohen, J.E. 1988. Untangling "an entangled bank": recent facts and theories about community food webs. Pp. 72-91 in: Community Ecology (A. Hastings, ed.). Springer-Verlag, New York, NY.

Cohen, J.E. 1989. Food webs and community structure. Pp. 181-202 in: Perspectives in Ecological Theory (J. Roughgarden, R.M. May, and S. Levin, eds.). PrincetonUniversity Press, Princeton, NJ.

Cohen, J.E., F. Briand, and C.M. Newman. 1989. Community Food Webs: Data and Theory. Springer-Verlag, New York, NY.

Cohen, J.E., and C.M. Newman. 1988. Dynamic basis of food web organization. Ecology 69:1655-1664.

Cohen, J.E., and C.M. Newman. 1991. Community area and food chain length: theoretical predictions. Am. Nat. 138:1542-1554.

DeAngelis, D.L. 1975. Stability and connectance in food web models. Ecology 56:238-243.

DeAngelis, D.L. 1992. Dynamics of Nutrient Cycling and Food Webs. Chapman and Hall, London, UK.

Ehrlich, P.R., and L.C. Birch. 1967. The "balance of nature" and "population control." Am. Nat. 101:97-107.

Fretwell, S. 1977. The regulation of plant communities by the food chains exploiting them. Perspect. Biol. Med. 20:169-185.

Gripenberg, S. and T. Roslin. 2007. Up or down in space? Uniting the bottom-up versus top-down paradigm and spatial ecology. Oikos 116:181-188.

Hairston, N.G., Jr., and N.G. Hairston, Sr. 1993. Cause-effect relationships in energy flow, trophic structure, and interspecific interactions. Am. Nat. 142:379-411.

Hairston, N.G., F.E. Smith, and L.B. Slobodkin. 1960. Community structure, population control, and competition. Am. Nat. 44:421-425.

Hall, S.J., and D. Raffaelli. 1991. Food-web patterns: lessons from a species-rich web. J. Anim. Ecol. 60:823-842.

Hunter, M.D., and P.W. Price. 1992. Playing chutes and ladders: heterogeneity and the relative roles of bottom-up and top-down forces in natural communities. Ecology 73:724-732.

Jenkins, B., R.L. Kitching, and S.L. Pimm. 1992. Productivity, disturbance, and food web structure ata local spatial scale in experimental container habitats. Oikos65:249-255.

Lawler, S.P., and P.J. Morin. 1993. Food web architecture and population dynamics in lab microcosms of protists. Am. Nat. 141:675-686.

Lawton, J.H. 1989. Food webs. Pp. 43-78 in: Ecological Concepts (J.M. Cherrett, ed.). Blackwell Scientific Publications, Oxford, UK.

Lawton, J.H., and P.H. Warren. 1988. Static and dynamic explanations for patterns in food webs. Trends Ecol. Evol. 3:242-245.

May, R.M. 1973. Stability and Complexity in Model Ecosystems.PrincetonUniv. Press, Princeton, NJ.

May, R. 1999. Unanswered questions in ecology. Phil. Trans. R. Soc. Lond. B 354-1951-1959.

Menge, B.A. 1992. Community regulation: under what conditions are bottom-up factors important on rocky shores? Ecology 73:755-765.

Moore, J.C., D.E. Walter, and H.W. Hunt. 1989. Habitat compartmentation and environmental correlates of food chain length. Science 243:238-239.

Murdoch, W.W. 1966. Community structure, population control, and competition: A critique. Am. Nat. 100:219-226.

Oksanen, L. 1988. Ecosystem organization: mutualism and cybernetics or plain Darwinian struggle for existence? Am. Nat. 131:424–444.

Oksanen, L., D. S. Fretwell, J. Arruda, and P. Niemela. 1981. Exploitation ecosystems in gradients of primary productivity. Am. Nat. 118:240-261.

Pahl-Wostl, C. 1993. Food webs and ecological networks across temporal and spatial scales. Oikos 66:415-432.

Paine, R.T. 1988. Food webs: road maps of interactions or grist for theoretical development? Ecology 69:1648-1654.

Persson, L., S. Diehl, L. Johansson, G. Andersson, and S.F. Hamrin. 1992. Trophic interactions in temperate lake ecosystems: a test of food chain theory. Am. Nat. 140:59-84.

Pimm, S.L. 1982. Food Webs. Chapman and Hall, London, UK.

Pimm, S.L., and J.H. Lawton. 1977. Number of trophic levels in ecological communities. Nature 268:329-331.

Pimm, S.L., and J.H. Lawton. 1978. On feeding on more than one trophic level. Nature 275:542-544.

Pimm, S.L., J.H. Lawton, and J.E. Cohen. 1991. Food web patterns and their consequences. Nature 350:669-674.

Polis, G.A. 1991. Complex desert food webs: an empirical critique of food web theory. Am. Nat. 138:123-155.

Polis, G.A. 1994. Food webs, trophic cascades and community structure. Aust. J. Ecol. 19:121- 136.

Power, M.E. 1992. Top-down and bottom-up forces in food webs: do plants have primacy? Ecology 73:733-746.

Rosemond, A.D., C.M. Pringle, A. Ramirez, and M.J. Paul. 2001. A test of top-down and bottom-up control in a detritus-based food web. Ecology 82:2279-2293.

Schoener, T.W. 1989. Food webs from the small to the large. Ecology 70:1559-1589.

Slobodkin, L.B., F.E. Smith, and N.G. Hairston. 1967. Regulation in terrestrial ecosystems, and the implied balance of nature. Am. Nat. 101:109-124.

Sterner, R.W., A. Bajpai, and T. Adams. 1997. The enigma of food chain length: absence of theoretical evidence for dynamic constraints. Ecology 78:2258-2262.

Strong, D.R. 1992. Are trophic cascades all wet? Differentiation and donor-control in speciose ecosystems. Ecology 73:747-754.

Terborgh, J., L. Lopez, P. Nuññez, M. Rao, G. Shahabuddin, G. Orihuela, M. Riveros, R. Ascanio, G.H. Adler, T.D. Lambert, and L. Balbas. 2001. Ecological meltdown in predator-free forest fragments. Science 294:1923-1926.

Walker, M., and T.H. Jones. 2001. Relative roles of top-down and bottom-up forces in terrestrial tritrophic plant-insect herbivore-natural enemy systems. Oikos 93:177-187.

Wiegert, R.G., and D.F. Owen. 1971. Trophic structure, available resources and population density in terrestrial vs. aquatic ecosystems. J. Theoret. Biol. 30:69-81.