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Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
PowerPoint Lectures for
Biology, Seventh Edition
Neil Campbell and Jane Reece
Lectures by Chris Romero
Chapter 53
Community Ecology
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Overview: What Is a Community?
• A biological community
– Is an assemblage of populations of various
species living close enough for potential
interaction
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The various animals and plants surrounding
this watering hole
– Are all members of a savanna community in
southern Africa
Figure 53.1
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Concept 53.1: A community’s interactions
include competition, predation, herbivory,
symbiosis, and disease
• Populations are linked by interspecific
interactions
– That affect the survival and reproduction of the
species engaged in the interaction
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Interspecific interactions
– Can have differing effects on the populations
involved
Table 53.1
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Competition
• Interspecific competition
– Occurs when species compete for a particular
resource that is in short supply
• Strong competition can lead to competitive
exclusion
– The local elimination of one of the two
competing species
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
The Competitive Exclusion Principle
• The competitive exclusion principle
– States that two species competing for the
same limiting resources cannot coexist in the
same place
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Ecological Niches
• The ecological niche
– Is the total of an organism’s use of the biotic
and abiotic resources in its environment
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• The niche concept allows restatement of the
competitive exclusion principle
– Two species cannot coexist in a community if
their niches are identical
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• However, ecologically similar species can
coexist in a community
– If there are one or more significant difference
in their niches
When Connell removed Balanus from the lower
strata, the Chthamalus population spread into that area.
The spread of Chthamalus when Balanus was
removed indicates that competitive exclusion makes the realized
niche of Chthamalus much smaller than its fundamental niche.
RESULTS
CONCLUSION
Ocean
Ecologist Joseph Connell studied two barnacle
speciesBalanus balanoides and Chthamalus stellatus that have a
stratified distribution on rocks along the coast of Scotland.
EXPERIMENT
In nature, Balanus fails to survive high on the rocks because it is
unable to resist desiccation (drying out) during low tides. Its realized
niche is therefore similar to its fundamental niche. In contrast,
Chthamalus is usually concentrated on the upper strata of rocks. To
determine the fundamental of niche of Chthamalus, Connell removed
Balanus from the lower strata.
Low tide
High tide
Chthamalus
fundamental niche
Chthamalus
realized niche
Low tide
High tide
Chthamalus
Balanus
realized niche
Balanus
Ocean
Figure 53.2
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• As a result of competition
– A species’ fundamental niche may be different
from its realized niche
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
A. insolitus
usually perches
on shady branches.
A. distichus perches
on fence posts and
other sunny
surfaces.
A. distichus
A. ricordii
A. insolitus
A. christophei
A. cybotes
A. etheridgei
A. alinigar
Figure 53.3
Resource Partitioning
• Resource partitioning is the differentiation of
niches
– That enables similar species to coexist in a
community
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
G. fortis
Beak depth (mm)
G. fuliginosa
Beak
depth
Los Hermanos
Daphne
Santa María, San Cristóbal
Sympatric
populations
G. fuliginosa,
allopatric
G. fortis, allopatric
Percentages
of
individuals
in
each
size
class
40
20
0
40
20
0
40
20
0
8 10 12 14 16
Figure 53.4
Character Displacement
• In character displacement
– There is a tendency for characteristics to be more
divergent in sympatric populations of two species
than in allopatric populations of the same two
species
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Predation
• Predation refers to an interaction
– Where one species, the predator, kills and eats
the other, the prey
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• Feeding adaptations of predators include
– Claws, teeth, fangs, stingers, and poison
• Animals also display
– A great variety of defensive adaptations
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• Cryptic coloration, or camouflage
– Makes prey difficult to spot
Figure 53.5
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• Aposematic coloration
– Warns predators to stay away from prey
Figure 53.6
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• In some cases, one prey species
– May gain significant protection by mimicking
the appearance of another
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• In Batesian mimicry
– A palatable or harmless species mimics an
unpalatable or harmful model
(a) Hawkmoth larva
(b) Green parrot snake
Figure 53.7a, b
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• In Müllerian mimicry
– Two or more unpalatable species resemble
each other
(a) Cuckoo bee
(b) Yellow jacket
Figure 53.8a, b
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Herbivory
• Herbivory, the process in which an herbivore
eats parts of a plant
– Has led to the evolution of plant mechanical
and chemical defenses and consequent
adaptations by herbivores
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Parasitism
• In parasitism, one organism, the parasite
– Derives its nourishment from another
organism, its host, which is harmed in the
process
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• Parasitism exerts substantial influence on
populations
– And the structure of communities
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Disease
• The effects of disease on populations and
communities
– Is similar to that of parasites
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• Pathogens, disease-causing agents
– Are typically bacteria, viruses, or protists
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Mutualism
• Mutualistic symbiosis, or mutualism
– Is an interspecific interaction that benefits both
species
Figure 53.9
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Commensalism
• In commensalism
– One species benefits and the other is not
affected
Figure 53.10
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• Commensal interactions have been difficult to
document in nature
– Because any close association between
species likely affects both species
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Interspecific Interactions and Adaptation
• Evidence for coevolution
– Which involves reciprocal genetic change by
interacting populations, is scarce
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• However, generalized adaptation of organisms
to other organisms in their environment
– Is a fundamental feature of life
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Concept 53.2: Dominant and keystone species
exert strong controls on community structure
• In general, a small number of species in a
community
– Exert strong control on that community’s
structure
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Species Diversity
• The species diversity of a community
– Is the variety of different kinds of organisms
that make up the community
– Has two components
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Species richness
– Is the total number of different species in the
community
• Relative abundance
– Is the proportion each species represents of
the total individuals in the community
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Two different communities
– Can have the same species richness, but a
different relative abundance
Community 1
A: 25% B: 25% C: 25% D: 25%
Community 2
A: 80% B: 5% C: 5% D: 10%
D
C
B
A
Figure 53.11
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• A community with an even species abundance
– Is more diverse than one in which one or two
species are abundant and the remainder rare
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Trophic Structure
• Trophic structure
– Is the feeding relationships between organisms
in a community
– Is a key factor in community dynamics
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Food chains
Quaternary
consumers
Tertiary
consumers
Secondary
consumers
Primary
consumers
Primary
producers
Carnivore
Carnivore
Carnivore
Herbivore
Plant
Carnivore
Carnivore
Carnivore
Zooplankton
Phytoplankton
A terrestrial food chain A marine food chain
Figure 53.12
– Link the trophic
levels from
producers to top
carnivores
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Food Webs
• A food web Humans
Baleen
whales
Crab-eater seals
Birds Fishes Squids
Leopard
seals
Elephant
seals
Smaller toothed
whales
Sperm
whales
Carnivorous
plankton
Euphausids
(krill)
Copepods
Phyto-
plankton
Figure 53.13
– Is a branching
food chain with
complex
trophic
interactions
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Food webs can be simplified
– By isolating a portion of a community that
interacts very little with the rest of the
community
Sea nettle
Fish larvae
Zooplankton
Fish eggs
Juvenile striped bass
Figure 53.14
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Limits on Food Chain Length
• Each food chain in a food web
– Is usually only a few links long
• There are two hypotheses
– That attempt to explain food chain length
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The energetic hypothesis suggests that the
length of a food chain
– Is limited by the inefficiency of energy transfer
along the chain
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The dynamic stability hypothesis
– Proposes that long food chains are less stable
than short ones
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Most of the available data
– Support the energetic hypothesis
High
(control)
Medium Low
Productivity
No. of species
No. of trophic
links
Number
of
species
Number
of
trophic
links
0
1
2
3
4
5
6
0
1
2
3
4
5
6
Figure 53.15
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Species with a Large Impact
• Certain species have an especially large
impact on the structure of entire communities
– Either because they are highly abundant or
because they play a pivotal role in community
dynamics
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Dominant Species
• Dominant species
– Are those species in a community that are
most abundant or have the highest biomass
– Exert powerful control over the occurrence and
distribution of other species
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• One hypothesis suggests that dominant
species
– Are most competitive in exploiting limited
resources
• Another hypothesis for dominant species
success
– Is that they are most successful at avoiding
predators
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Keystone Species
• Keystone species
– Are not necessarily abundant in a community
– Exert strong control on a community by their
ecological roles, or niches
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Field studies of sea stars
– Exhibit their role as a keystone species in intertidal
communities
Figure 53.16a,b
(a) The sea star Pisaster ochraceous feeds
preferentially on mussels but will
consume other invertebrates.
With Pisaster (control)
Without Pisaster (experimental)
Number
of
species
present
0
5
10
15
20
1963 ´64 ´65 ´66 ´67 ´68 ´69 ´70 ´71 ´72 ´73
(b) When Pisaster was removed from an intertidal zone,
mussels eventually took over the rock face and eliminated
most other invertebrates and algae. In a control area from
which Pisaster was not removed, there was little change
in species diversity.
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Observation of sea otter populations and their
predation
Figure 53.17
Food chain before
killer whale involve-
ment in chain
(a) Sea otter abundance
(b) Sea urchin biomass
(c) Total kelp density
Number
per
0.25
m
2
1972 1985 1989 1993 1997
0
2
4
6
8
10
0
100
200
300
400
Grams
per
0.25
m
2
Otter
number
(%
max.
count)
0
40
20
60
80
100
Year
Food chain after killer
whales started preying
on otters
– Shows the
effect the
otters have
on ocean
communities
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Ecosystem “Engineers” (Foundation Species)
• Some organisms exert their influence
– By causing physical changes in the
environment that affect community structure
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Beaver dams
– Can transform landscapes on a very large
scale
Figure 53.18
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Some foundation species act as facilitators
– That have positive effects on the survival and
reproduction of some of the other species in the
community
Figure 53.19
Salt marsh with Juncus
(foreground)
With
Juncus
Without
Juncus
Number
of
plant
species
0
2
4
6
8
Conditions
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Bottom-Up and Top-Down Controls
• The bottom-up model of community
organization
– Proposes a unidirectional influence from lower
to higher trophic levels
• In this case, the presence or absence of abiotic
nutrients
– Determines community structure, including the
abundance of primary producers
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The top-down model of community
organization
– Proposes that control comes from the trophic
level above
• In this case, predators control herbivores
– Which in turn control primary producers
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Long-term experiment studies have shown
– That communities can shift periodically from
bottom-up to top-down
Figure 53.20
0 100 200 300 400
Rainfall (mm)
0
25
50
75
100
Percentage
of
herbaceous
plant
cover
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Pollution
– Can affect community dynamics
• But through biomanipulation
– Polluted communities can be restored
Fish
Zooplankton
Algae
Abundant
Rare
Rare
Abundant
Abundant
Rare
Polluted State Restored State
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Concept 53.3: Disturbance influences species
diversity and composition
• Decades ago, most ecologists favored the
traditional view
– That communities are in a state of equilibrium
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• However, a recent emphasis on change has
led to a nonequilibrium model
– Which describes communities as constantly
changing after being buffeted by disturbances
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
What Is Disturbance?
• A disturbance
– Is an event that changes a community
– Removes organisms from a community
– Alters resource availability
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Fire
– Is a significant disturbance in most terrestrial
ecosystems
– Is often a necessity in some communities
(a) Before a controlled burn.
A prairie that has not burned for
several years has a high propor-
tion of detritus (dead grass).
(b) During the burn. The detritus
serves as fuel for fires.
(c) After the burn. Approximately one
month after the controlled burn,
virtually all of the biomass in this
prairie is living.
Figure 53.21a–c
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The intermediate disturbance hypothesis
– Suggests that moderate levels of disturbance
can foster higher species diversity than low
levels of disturbance
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The large-scale fire in Yellowstone National
Park in 1988
– Demonstrated that communities can often
respond very rapidly to a massive disturbance
Figure 53.22a, b
(a) Soon after fire. As this photo taken soon after the fire shows,
the burn left a patchy landscape. Note the unburned trees in the
distance.
(b) One year after fire. This photo of the same general area taken the
following year indicates how rapidly the community began to
recover. A variety of herbaceous plants, different from those in the
former forest, cover the ground.
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Human Disturbance
• Humans
– Are the most widespread agents of
disturbance
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Human disturbance to communities
– Usually reduces species diversity
• Humans also prevent some naturally occurring
disturbances
– Which can be important to community
structure
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Ecological Succession
• Ecological succession
– Is the sequence of community and ecosystem
changes after a disturbance
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• Primary succession
– Occurs where no soil exists when succession
begins
• Secondary succession
– Begins in an area where soil remains after a
disturbance
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Early-arriving species
– May facilitate the appearance of later species
by making the environment more favorable
– May inhibit establishment of later species
– May tolerate later species but have no impact
on their establishment
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
McBride glacier retreating
0 5 10
Miles
Glacier
Bay
Pleasant Is.
Johns Hopkins
Gl.
Reid Gl.
Grand
Pacific Gl.
Canada
Alaska
1940 1912
1899
1879
1879
1949
1879
1935
1760
1780
1830
1860
1913
1911
1892
1900
1879
1907 1948
1931
1941
1948
• Retreating glaciers
– Provide a valuable field-research opportunity on
succession
Figure 53.23
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Succession on the moraines in Glacier Bay, Alaska
– Follows a predictable pattern of change in vegetation
and soil characteristics
Figure 53.24a–d
(b) Dryas stage
(c) Spruce stage
(d) Nitrogen fixation by Dryas and alder
increases the soil nitrogen content.
Soil
nitrogen
(g/m
2
)
Successional stage
Pioneer Dryas Alder Spruce
0
10
20
30
40
50
60
(a) Pioneer stage, with fireweed dominant
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Concept 53.4: Biogeographic factors affect
community diversity
• Two key factors correlated with a community’s
species diversity
– Are its geographic location and its size
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Equatorial-Polar Gradients
• The two key factors in equatorial-polar
gradients of species richness
– Are probably evolutionary history and climate
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Species richness generally declines along an
equatorial-polar gradient
– And is especially great in the tropics
• The greater age of tropical environments
– May account for the greater species richness
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Climate
– Is likely the primary cause of the latitudinal
gradient in biodiversity
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The two main climatic factors correlated with
biodiversity
– Are solar energy input and water availability
(b) Vertebrates
500 1,000 1,500 2,000
Potential evapotranspiration (mm/yr)
10
50
100
200
Vertebrate
species
richness
(log
scale)
1
100 300 500 700 900 1,100
180
160
140
120
100
80
60
40
20
0
Tree
species
richness
(a) Trees
Actual evapotranspiration (mm/yr)
Figure 53.25a, b
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Area Effects
• The species-area curve quantifies the idea that
– All other factors being equal, the larger the
geographic area of a community, the greater
the number of species
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• A species-area curve of North American
breeding birds
– Supports this idea
Area (acres)
1 10 100 103 104 105 106 107 108 109 1010
Number
of
species
(log
scale)
1
10
100
1,000
Figure 53.26
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Island Equilibrium Model
• Species richness on islands
– Depends on island size, distance from the
mainland, immigration, and extinction
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Figure 53.27a–c
• The equilibrium model of island biogeography
maintains that
– Species richness on an ecological island
levels off at some dynamic equilibrium point
Number of species on island
(a) Immigration and extinction rates. The
equilibrium number of species on an
island represents a balance between the
immigration of new species and the
extinction of species already there.
(b) Effect of island size. Large islands may
ultimately have a larger equilibrium num-
ber of species than small islands because
immigration rates tend to be higher and
extinction rates lower on large islands.
Number of species on island Number of species on island
(c) Effect of distance from mainland.
Near islands tend to have larger
equilibrium numbers of species than
far islands because immigration rates
to near islands are higher and extinction
rates lower.
Equilibrium number Small island Large island Far island Near island
Rate
of
immigration
or
extinction
Rate
of
immigration
or
extinction
Rate
of
immigration
or
extinction
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Studies of species richness on the Galápagos Islands
– Support the prediction that species richness
increases with island size
The results of the study showed that plant species
richness increased with island size, supporting the species-area theory.
FIELD STUDY
RESULTS
Ecologists Robert MacArthur and E. O. Wilson studied the
number of plant species on the Galápagos Islands, which vary greatly in size, in
relation to the area of each island.
CONCLUSION
200
100
50
25
10
0
Area of island (mi2)
(log scale)
Number
of
plant
species
(log
scale)
0.1 1 10 100 1,000
5
400
Figure 53.28
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Concept 53.5: Contrasting views of community
structure are the subject of continuing debate
• Two different views on community structure
– Emerged among ecologists in the 1920s and
1930s
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Integrated and Individualistic Hypotheses
• The integrated hypothesis of community
structure
– Describes a community as an assemblage of
closely linked species, locked into association
by mandatory biotic interactions
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The individualistic hypothesis of community
structure
– Proposes that communities are loosely
organized associations of independently
distributed species with the same abiotic
requirements
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The integrated hypothesis
– Predicts that the presence or absence of
particular species depends on the presence or
absence of other species
Population
densities
of
individual
species
Environmental gradient
(such as temperature or moisture)
(a) Integrated hypothesis. Communities are discrete groupings
of particular species that are closely interdependent and nearly
always occur together.
Figure 53.29a
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The individualistic hypothesis
– Predicts that each species is distributed
according to its tolerance ranges for abiotic
factors
Population
densities
of
individual
species
Environmental gradient
(such as temperature or moisture)
(b) Individualistic hypothesis. Species are independently
distributed along gradients and a community is simply the
assemblage of species that occupy the same area because of
similar abiotic needs.
Figure 53.29b
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• In most actual cases the composition of
communities
– Seems to change continuously, with each
species more or less independently distributed
Number
of
plants
per
hectare
Wet Moisture gradient Dry
(c) Trees in the Santa Catalina Mountains. The distribution of tree species at one
elevation in the Santa Catalina Mountains of Arizona supports the individualistic
hypothesis. Each tree species has an independent distribution along the gradient,
apparently conforming to its tolerance for moisture, and the species that live
together at any point along the gradient have similar physical requirements.
Because the vegetation changes continuously along the gradient, it is impossible to
delimit sharp boundaries for the communities.
0
200
400
600
Figure 53.29c
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Rivet and Redundancy Models
• The rivet model of communities
– Suggests that all species in a community are
linked together in a tight web of interactions
– Also states that the loss of even a single
species has strong repercussions for the
community
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• The redundancy model of communities
– Proposes that if a species is lost from a
community, other species will fill the gap
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• It is important to keep in mind that community
hypotheses and models
– Represent extremes, and that most
communities probably lie somewhere in the
middle

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53_COMMUNITY_ECOLOGY_ppt.ppt

  • 1. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece Lectures by Chris Romero Chapter 53 Community Ecology
  • 2. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Overview: What Is a Community? • A biological community – Is an assemblage of populations of various species living close enough for potential interaction
  • 3. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The various animals and plants surrounding this watering hole – Are all members of a savanna community in southern Africa Figure 53.1
  • 4. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Concept 53.1: A community’s interactions include competition, predation, herbivory, symbiosis, and disease • Populations are linked by interspecific interactions – That affect the survival and reproduction of the species engaged in the interaction
  • 5. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Interspecific interactions – Can have differing effects on the populations involved Table 53.1
  • 6. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Competition • Interspecific competition – Occurs when species compete for a particular resource that is in short supply • Strong competition can lead to competitive exclusion – The local elimination of one of the two competing species
  • 7. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings The Competitive Exclusion Principle • The competitive exclusion principle – States that two species competing for the same limiting resources cannot coexist in the same place
  • 8. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Ecological Niches • The ecological niche – Is the total of an organism’s use of the biotic and abiotic resources in its environment
  • 9. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The niche concept allows restatement of the competitive exclusion principle – Two species cannot coexist in a community if their niches are identical
  • 10. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • However, ecologically similar species can coexist in a community – If there are one or more significant difference in their niches When Connell removed Balanus from the lower strata, the Chthamalus population spread into that area. The spread of Chthamalus when Balanus was removed indicates that competitive exclusion makes the realized niche of Chthamalus much smaller than its fundamental niche. RESULTS CONCLUSION Ocean Ecologist Joseph Connell studied two barnacle speciesBalanus balanoides and Chthamalus stellatus that have a stratified distribution on rocks along the coast of Scotland. EXPERIMENT In nature, Balanus fails to survive high on the rocks because it is unable to resist desiccation (drying out) during low tides. Its realized niche is therefore similar to its fundamental niche. In contrast, Chthamalus is usually concentrated on the upper strata of rocks. To determine the fundamental of niche of Chthamalus, Connell removed Balanus from the lower strata. Low tide High tide Chthamalus fundamental niche Chthamalus realized niche Low tide High tide Chthamalus Balanus realized niche Balanus Ocean Figure 53.2
  • 11. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • As a result of competition – A species’ fundamental niche may be different from its realized niche
  • 12. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings A. insolitus usually perches on shady branches. A. distichus perches on fence posts and other sunny surfaces. A. distichus A. ricordii A. insolitus A. christophei A. cybotes A. etheridgei A. alinigar Figure 53.3 Resource Partitioning • Resource partitioning is the differentiation of niches – That enables similar species to coexist in a community
  • 13. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings G. fortis Beak depth (mm) G. fuliginosa Beak depth Los Hermanos Daphne Santa María, San Cristóbal Sympatric populations G. fuliginosa, allopatric G. fortis, allopatric Percentages of individuals in each size class 40 20 0 40 20 0 40 20 0 8 10 12 14 16 Figure 53.4 Character Displacement • In character displacement – There is a tendency for characteristics to be more divergent in sympatric populations of two species than in allopatric populations of the same two species
  • 14. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Predation • Predation refers to an interaction – Where one species, the predator, kills and eats the other, the prey
  • 15. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Feeding adaptations of predators include – Claws, teeth, fangs, stingers, and poison • Animals also display – A great variety of defensive adaptations
  • 16. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Cryptic coloration, or camouflage – Makes prey difficult to spot Figure 53.5
  • 17. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Aposematic coloration – Warns predators to stay away from prey Figure 53.6
  • 18. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • In some cases, one prey species – May gain significant protection by mimicking the appearance of another
  • 19. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • In Batesian mimicry – A palatable or harmless species mimics an unpalatable or harmful model (a) Hawkmoth larva (b) Green parrot snake Figure 53.7a, b
  • 20. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • In Müllerian mimicry – Two or more unpalatable species resemble each other (a) Cuckoo bee (b) Yellow jacket Figure 53.8a, b
  • 21. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Herbivory • Herbivory, the process in which an herbivore eats parts of a plant – Has led to the evolution of plant mechanical and chemical defenses and consequent adaptations by herbivores
  • 22. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Parasitism • In parasitism, one organism, the parasite – Derives its nourishment from another organism, its host, which is harmed in the process
  • 23. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Parasitism exerts substantial influence on populations – And the structure of communities
  • 24. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Disease • The effects of disease on populations and communities – Is similar to that of parasites
  • 25. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Pathogens, disease-causing agents – Are typically bacteria, viruses, or protists
  • 26. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Mutualism • Mutualistic symbiosis, or mutualism – Is an interspecific interaction that benefits both species Figure 53.9
  • 27. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Commensalism • In commensalism – One species benefits and the other is not affected Figure 53.10
  • 28. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Commensal interactions have been difficult to document in nature – Because any close association between species likely affects both species
  • 29. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Interspecific Interactions and Adaptation • Evidence for coevolution – Which involves reciprocal genetic change by interacting populations, is scarce
  • 30. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • However, generalized adaptation of organisms to other organisms in their environment – Is a fundamental feature of life
  • 31. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Concept 53.2: Dominant and keystone species exert strong controls on community structure • In general, a small number of species in a community – Exert strong control on that community’s structure
  • 32. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Species Diversity • The species diversity of a community – Is the variety of different kinds of organisms that make up the community – Has two components
  • 33. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Species richness – Is the total number of different species in the community • Relative abundance – Is the proportion each species represents of the total individuals in the community
  • 34. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Two different communities – Can have the same species richness, but a different relative abundance Community 1 A: 25% B: 25% C: 25% D: 25% Community 2 A: 80% B: 5% C: 5% D: 10% D C B A Figure 53.11
  • 35. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • A community with an even species abundance – Is more diverse than one in which one or two species are abundant and the remainder rare
  • 36. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Trophic Structure • Trophic structure – Is the feeding relationships between organisms in a community – Is a key factor in community dynamics
  • 37. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Food chains Quaternary consumers Tertiary consumers Secondary consumers Primary consumers Primary producers Carnivore Carnivore Carnivore Herbivore Plant Carnivore Carnivore Carnivore Zooplankton Phytoplankton A terrestrial food chain A marine food chain Figure 53.12 – Link the trophic levels from producers to top carnivores
  • 38. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Food Webs • A food web Humans Baleen whales Crab-eater seals Birds Fishes Squids Leopard seals Elephant seals Smaller toothed whales Sperm whales Carnivorous plankton Euphausids (krill) Copepods Phyto- plankton Figure 53.13 – Is a branching food chain with complex trophic interactions
  • 39. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Food webs can be simplified – By isolating a portion of a community that interacts very little with the rest of the community Sea nettle Fish larvae Zooplankton Fish eggs Juvenile striped bass Figure 53.14
  • 40. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Limits on Food Chain Length • Each food chain in a food web – Is usually only a few links long • There are two hypotheses – That attempt to explain food chain length
  • 41. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The energetic hypothesis suggests that the length of a food chain – Is limited by the inefficiency of energy transfer along the chain
  • 42. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The dynamic stability hypothesis – Proposes that long food chains are less stable than short ones
  • 43. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Most of the available data – Support the energetic hypothesis High (control) Medium Low Productivity No. of species No. of trophic links Number of species Number of trophic links 0 1 2 3 4 5 6 0 1 2 3 4 5 6 Figure 53.15
  • 44. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Species with a Large Impact • Certain species have an especially large impact on the structure of entire communities – Either because they are highly abundant or because they play a pivotal role in community dynamics
  • 45. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Dominant Species • Dominant species – Are those species in a community that are most abundant or have the highest biomass – Exert powerful control over the occurrence and distribution of other species
  • 46. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • One hypothesis suggests that dominant species – Are most competitive in exploiting limited resources • Another hypothesis for dominant species success – Is that they are most successful at avoiding predators
  • 47. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Keystone Species • Keystone species – Are not necessarily abundant in a community – Exert strong control on a community by their ecological roles, or niches
  • 48. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Field studies of sea stars – Exhibit their role as a keystone species in intertidal communities Figure 53.16a,b (a) The sea star Pisaster ochraceous feeds preferentially on mussels but will consume other invertebrates. With Pisaster (control) Without Pisaster (experimental) Number of species present 0 5 10 15 20 1963 ´64 ´65 ´66 ´67 ´68 ´69 ´70 ´71 ´72 ´73 (b) When Pisaster was removed from an intertidal zone, mussels eventually took over the rock face and eliminated most other invertebrates and algae. In a control area from which Pisaster was not removed, there was little change in species diversity.
  • 49. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Observation of sea otter populations and their predation Figure 53.17 Food chain before killer whale involve- ment in chain (a) Sea otter abundance (b) Sea urchin biomass (c) Total kelp density Number per 0.25 m 2 1972 1985 1989 1993 1997 0 2 4 6 8 10 0 100 200 300 400 Grams per 0.25 m 2 Otter number (% max. count) 0 40 20 60 80 100 Year Food chain after killer whales started preying on otters – Shows the effect the otters have on ocean communities
  • 50. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Ecosystem “Engineers” (Foundation Species) • Some organisms exert their influence – By causing physical changes in the environment that affect community structure
  • 51. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Beaver dams – Can transform landscapes on a very large scale Figure 53.18
  • 52. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Some foundation species act as facilitators – That have positive effects on the survival and reproduction of some of the other species in the community Figure 53.19 Salt marsh with Juncus (foreground) With Juncus Without Juncus Number of plant species 0 2 4 6 8 Conditions
  • 53. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Bottom-Up and Top-Down Controls • The bottom-up model of community organization – Proposes a unidirectional influence from lower to higher trophic levels • In this case, the presence or absence of abiotic nutrients – Determines community structure, including the abundance of primary producers
  • 54. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The top-down model of community organization – Proposes that control comes from the trophic level above • In this case, predators control herbivores – Which in turn control primary producers
  • 55. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Long-term experiment studies have shown – That communities can shift periodically from bottom-up to top-down Figure 53.20 0 100 200 300 400 Rainfall (mm) 0 25 50 75 100 Percentage of herbaceous plant cover
  • 56. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Pollution – Can affect community dynamics • But through biomanipulation – Polluted communities can be restored Fish Zooplankton Algae Abundant Rare Rare Abundant Abundant Rare Polluted State Restored State
  • 57. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Concept 53.3: Disturbance influences species diversity and composition • Decades ago, most ecologists favored the traditional view – That communities are in a state of equilibrium
  • 58. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • However, a recent emphasis on change has led to a nonequilibrium model – Which describes communities as constantly changing after being buffeted by disturbances
  • 59. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings What Is Disturbance? • A disturbance – Is an event that changes a community – Removes organisms from a community – Alters resource availability
  • 60. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Fire – Is a significant disturbance in most terrestrial ecosystems – Is often a necessity in some communities (a) Before a controlled burn. A prairie that has not burned for several years has a high propor- tion of detritus (dead grass). (b) During the burn. The detritus serves as fuel for fires. (c) After the burn. Approximately one month after the controlled burn, virtually all of the biomass in this prairie is living. Figure 53.21a–c
  • 61. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The intermediate disturbance hypothesis – Suggests that moderate levels of disturbance can foster higher species diversity than low levels of disturbance
  • 62. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The large-scale fire in Yellowstone National Park in 1988 – Demonstrated that communities can often respond very rapidly to a massive disturbance Figure 53.22a, b (a) Soon after fire. As this photo taken soon after the fire shows, the burn left a patchy landscape. Note the unburned trees in the distance. (b) One year after fire. This photo of the same general area taken the following year indicates how rapidly the community began to recover. A variety of herbaceous plants, different from those in the former forest, cover the ground.
  • 63. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Human Disturbance • Humans – Are the most widespread agents of disturbance
  • 64. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Human disturbance to communities – Usually reduces species diversity • Humans also prevent some naturally occurring disturbances – Which can be important to community structure
  • 65. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Ecological Succession • Ecological succession – Is the sequence of community and ecosystem changes after a disturbance
  • 66. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Primary succession – Occurs where no soil exists when succession begins • Secondary succession – Begins in an area where soil remains after a disturbance
  • 67. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Early-arriving species – May facilitate the appearance of later species by making the environment more favorable – May inhibit establishment of later species – May tolerate later species but have no impact on their establishment
  • 68. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings McBride glacier retreating 0 5 10 Miles Glacier Bay Pleasant Is. Johns Hopkins Gl. Reid Gl. Grand Pacific Gl. Canada Alaska 1940 1912 1899 1879 1879 1949 1879 1935 1760 1780 1830 1860 1913 1911 1892 1900 1879 1907 1948 1931 1941 1948 • Retreating glaciers – Provide a valuable field-research opportunity on succession Figure 53.23
  • 69. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Succession on the moraines in Glacier Bay, Alaska – Follows a predictable pattern of change in vegetation and soil characteristics Figure 53.24a–d (b) Dryas stage (c) Spruce stage (d) Nitrogen fixation by Dryas and alder increases the soil nitrogen content. Soil nitrogen (g/m 2 ) Successional stage Pioneer Dryas Alder Spruce 0 10 20 30 40 50 60 (a) Pioneer stage, with fireweed dominant
  • 70. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Concept 53.4: Biogeographic factors affect community diversity • Two key factors correlated with a community’s species diversity – Are its geographic location and its size
  • 71. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Equatorial-Polar Gradients • The two key factors in equatorial-polar gradients of species richness – Are probably evolutionary history and climate
  • 72. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Species richness generally declines along an equatorial-polar gradient – And is especially great in the tropics • The greater age of tropical environments – May account for the greater species richness
  • 73. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Climate – Is likely the primary cause of the latitudinal gradient in biodiversity
  • 74. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The two main climatic factors correlated with biodiversity – Are solar energy input and water availability (b) Vertebrates 500 1,000 1,500 2,000 Potential evapotranspiration (mm/yr) 10 50 100 200 Vertebrate species richness (log scale) 1 100 300 500 700 900 1,100 180 160 140 120 100 80 60 40 20 0 Tree species richness (a) Trees Actual evapotranspiration (mm/yr) Figure 53.25a, b
  • 75. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Area Effects • The species-area curve quantifies the idea that – All other factors being equal, the larger the geographic area of a community, the greater the number of species
  • 76. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • A species-area curve of North American breeding birds – Supports this idea Area (acres) 1 10 100 103 104 105 106 107 108 109 1010 Number of species (log scale) 1 10 100 1,000 Figure 53.26
  • 77. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Island Equilibrium Model • Species richness on islands – Depends on island size, distance from the mainland, immigration, and extinction
  • 78. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 53.27a–c • The equilibrium model of island biogeography maintains that – Species richness on an ecological island levels off at some dynamic equilibrium point Number of species on island (a) Immigration and extinction rates. The equilibrium number of species on an island represents a balance between the immigration of new species and the extinction of species already there. (b) Effect of island size. Large islands may ultimately have a larger equilibrium num- ber of species than small islands because immigration rates tend to be higher and extinction rates lower on large islands. Number of species on island Number of species on island (c) Effect of distance from mainland. Near islands tend to have larger equilibrium numbers of species than far islands because immigration rates to near islands are higher and extinction rates lower. Equilibrium number Small island Large island Far island Near island Rate of immigration or extinction Rate of immigration or extinction Rate of immigration or extinction
  • 79. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Studies of species richness on the Galápagos Islands – Support the prediction that species richness increases with island size The results of the study showed that plant species richness increased with island size, supporting the species-area theory. FIELD STUDY RESULTS Ecologists Robert MacArthur and E. O. Wilson studied the number of plant species on the Galápagos Islands, which vary greatly in size, in relation to the area of each island. CONCLUSION 200 100 50 25 10 0 Area of island (mi2) (log scale) Number of plant species (log scale) 0.1 1 10 100 1,000 5 400 Figure 53.28
  • 80. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • Concept 53.5: Contrasting views of community structure are the subject of continuing debate • Two different views on community structure – Emerged among ecologists in the 1920s and 1930s
  • 81. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Integrated and Individualistic Hypotheses • The integrated hypothesis of community structure – Describes a community as an assemblage of closely linked species, locked into association by mandatory biotic interactions
  • 82. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The individualistic hypothesis of community structure – Proposes that communities are loosely organized associations of independently distributed species with the same abiotic requirements
  • 83. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The integrated hypothesis – Predicts that the presence or absence of particular species depends on the presence or absence of other species Population densities of individual species Environmental gradient (such as temperature or moisture) (a) Integrated hypothesis. Communities are discrete groupings of particular species that are closely interdependent and nearly always occur together. Figure 53.29a
  • 84. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The individualistic hypothesis – Predicts that each species is distributed according to its tolerance ranges for abiotic factors Population densities of individual species Environmental gradient (such as temperature or moisture) (b) Individualistic hypothesis. Species are independently distributed along gradients and a community is simply the assemblage of species that occupy the same area because of similar abiotic needs. Figure 53.29b
  • 85. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • In most actual cases the composition of communities – Seems to change continuously, with each species more or less independently distributed Number of plants per hectare Wet Moisture gradient Dry (c) Trees in the Santa Catalina Mountains. The distribution of tree species at one elevation in the Santa Catalina Mountains of Arizona supports the individualistic hypothesis. Each tree species has an independent distribution along the gradient, apparently conforming to its tolerance for moisture, and the species that live together at any point along the gradient have similar physical requirements. Because the vegetation changes continuously along the gradient, it is impossible to delimit sharp boundaries for the communities. 0 200 400 600 Figure 53.29c
  • 86. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Rivet and Redundancy Models • The rivet model of communities – Suggests that all species in a community are linked together in a tight web of interactions – Also states that the loss of even a single species has strong repercussions for the community
  • 87. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • The redundancy model of communities – Proposes that if a species is lost from a community, other species will fill the gap
  • 88. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings • It is important to keep in mind that community hypotheses and models – Represent extremes, and that most communities probably lie somewhere in the middle