Biology II

Chapter 48 Notes

A community consists of all the organisms inhabiting a particular area; an assemblage of populations of different species living close enough together for potential interaction.

I. The interactive and individualistic hyptheses pose alternative explanations of community structure: science as a process.

Among the pioneers of community ecology, there were two divergent views on why certain combinations of species are found together as members of a community: the individualistic hypothesis and the interactive hypothesis.

The individualistic hypothesis was proposed by H.A. Gleason. This hypothesis depicted a community as a chance assemblage of species found in an area because they have similar environmental requirements.

· Emphasizes studying single species.

· Predicts each species will have an independent distribution along an environmental gradient and there are no discrete geographical boundaries between communities.

· In most cases, the composition of communities would change continuously along some environmental gradient to do addition or loss of particular species.

The interactive hypothesis proposed by F.E. Clements saw each community as an assemblage of closely linked species having mandatory biotic interactions that cause the community to function as an integrated unit.

· Based on the fact that certain plant species are consistently found together

· Emphasizes entire assemblages of species as the essential units for understanding the interrelationships and distributions of organisms.

· Predicts species should be clustered, with discrete boundaries between communities. Since the presence or absence of one species is governed by the presence or absence or other species with which it interacts.

· Not generally seen in plants, especially where broad regions are characterized by gradients of environmental variation.

Animals in a community are often linked more rigidly to other organisms.

· Some animals feed primarily on certain food items so their distributions is linked to distributions of the food source.

· Other animals feed on a variety of food items and tend to be distributed in a variety of communities.

Distribution of almost all organisms is affected by both abiotic gradients and interactions with other species.

II. Community interactions can provide strong selection factors in evolution.

· Interactions between species are as important to adaptation by natural selection as the physical and chemical features of the environment.

Coevolution- A change in one species acts as a new selective force on

Another species, and counteradaptation of the second species, in turn, affects selection of individuals in the first species.

· Studied most extensively in predator-prey relationships and in mutualism.

· Often, what appears to be coevolution may actually result from interactions with many species (not just the obvious two).

The association between passionflower vines (Passiflora) and the butterfly Heliconius is believed to be an example of coevoltuion.

· The vines produce toxic chemicals to reduce damage to young shoots and leaves by herbivorous insects.

· Butterfly larvae of Heliconius can tolerate these chemicals due to digestive enzymes, which break down the toxic chemicals (a counteradaptation).

· Females of some Heliconius species avoid laying eggs (which are bright yellow) on leaves where other yellow egg clusters have been laid.

ð This reduces intraspecific competition on individual leaves.

· Some species of passionflowers develop large, yellow nectaires which resemble Heliconius eggs; and adaptation that may divert egg-laying butterflies to other plants.

· These nectaires, as well as smaller ones, also attract ants and wasps which prey on butterfly eggs and larvae.

Biologists agree that adaptation of organisms to other species in a community is a fundamental characteristic of life.

III. Interspecific interactions may have positive, negative, or neutral effects on a population’s density: an overview

While adaptations to abiotic factors largely determine the geographic distributions of many species, all organisms are influenced by biotic interactions with other individuals.

· Intraspecific competitions for resources was discussed in Chapter 47.

· Interspecific interactions are those that occur between populations of different species living in a community.

ð May take a variety of forms.

The two species involved in the interaction may have a (+), negative (-), or neutral (0) effect on their population densities.

· Both population densities may increase (++), one may increase while the other decreases (+ -_, on may increase while the other is not affected (+0), or both may decrease (- -). (See Campbell, Table 48.1)

IV. Predation and parasitism are (+ -) interactions: a closer look

There are several (+ -) interactions, some are obvious, some are not.

· Predation involves a predator which eats is prey.

· Parasitism involves predators which live in or on their hosts and seldom involves outright host death.

· Parasitoidism involves insects such as small wasps who lay their eggs on living hosts – after hatching, the larvae feed within the host’s body and eventually cause its death.

· Herbivory occurs when animals eat plants. May only cuase damage to a portion of the plant (grazing) or may kill an entire plant (seed eating)

A. Predation

Predation= A community interaction where one species, the predator, eats another, the prey. Includes both animal-animal interactions and animal-plant interactions.

Adaptations of predators to this interaction are obvious and familiar, Predators have:

· Acute senses that are used to locate and identify prey items (e.g. heat-sensing pits of rattlesnakes, and chemical sensors of herbivorous insects).

· Structures such as claws, teeth, fangs, stingers, and poisons which function to catch, subdue, or chew the prey item.

· Speed and agility to pursue prey or camouflage which permits them to ambush prey.

Various defensive adaptations have evolved in prey species as a result of repeated encounters with predators over evolutionary time.

1. Plant Defenses Against Herbivores

Since plants cannot escape herbivores, they have evolved several ways to protect themselves from predation.

Plants have mechanical and chemical defenses against herbivores.

· Thorns or microscopic hooks, spines, and crystals may be present to discourage herbivores.

· May produce secondary compounds (formed as by-products of major metabolic pathways) that make vegetation distasteful or harmful.

· May produce analogues of insect hormones that cause abnormal development in insects that prey on them

Plant defenses may act as selective factors leading to counteradaptations in herbivores that can then nullify those defenses and consume the plant.

2. Animal Defenses Against Predators

Animal defenses against predators may be passive (hiding), active (escaping and physical defense), or chemical based.

Other forms of defense involving adaptive coloration have evolved repeatedly among animals.

· Cryptic coloration (coloration making prey difficult to spot against its surroundings) is common and only requires they animal to remain still to avoid detection.

· Deceptive marking such as large, fake eyes can startle predators, allowing prey to escape, or cause predators to strike a nonvital area.

· Some mechanical and chemical defenses actively discourage predators (e.g. porcupine quills and skunk spray).

· Some insects acquire chemical defense passively by accumulating toxins from plants they eat; these make them distasteful to predators.

· Aposematic coloration (Bright coloration that acts as a warning of effective physical or chemical defense) appears to be adaptive since predators quickly learn to avoid prey with this coloration.

3. Mimicry

Mimicry is a phenomenon in which a mimic bears a superficial resemblance to another species, the model.

· Occurs in both predatory and prey species.

· Defensive mimicry in prey usually involves aposematic modles.

Batesian mimicry= A palatable species mimics an unpalatable or harmful model.

· Mimic must be much less abundant than the model to be effective since predators must learn the coloration indicates a bad or harmful food item.

Mullerian mimicry= Two or more unpalatable, aposematically colored species resemble each other.

· Each gains additional advantage since predators learn more quickly to avoid prey with this coloration.

Predators also use mimicry to lure prey.

· They tongue of snapping turtles resembles a wriggling worn which attracts small fish into capture range.

B. Parasitism

Parasitism is a (+ -) interaction in which one organism, the parasite, derives its nourishment from another organism, the host, which is harmed in some way.

· Endoparasites live within the host tissues or body cavities.

· Ectoparasites attach to or briefly feed on the external surface of the host.

Natural selection favors parasites that are best able to locate and feed on a host.

· Infection by a parasite (locating a host) may be passive as when an endoparasite’s egg is swallowed by a host.

· Active location of a host may involve thermal or chemical cues that help the parasite identify the host.

Defensive capabilities in potential hosts have also been selected for by natural selection.

· Secondary plant products toxic to herbivores may also be toxic to parasitic fungi and bacteria.

· The vertebrate immune system provides defense against endoparasites.

· Many parasites are adapted to specific hosts, often a single species.

· Coevolution generally results in stable relationships in which the host is not killed (host death would also kill the parasite).

Some forms of parasitism do not involve the consumption of the host, but are the exploitation of the host’s behavior by the parasite. For example, in brood parasitism:

· Some species of birds (cowbirds, European cuckoos) lay their eggs in the nests of other species.

· Often a newly hatched brood parasite will move other eggs out of the nest.

· Host parents invest their energy in feeding the brood parasite instead of their own offspring- a (+ -) interaction.

· An evolutionary adaptation in many host species is the ability to detect parasite eggs which are removed or the nest is abandoned.

ð A counter- adaptation to this host defense is egg mimicry in some brood parasites.

V. Interspecific competitions are (- -) interactions: a closer look

Interspecific competition occurs when two or more species in a community rely on similar limiting resources.

· May take the form of interference competition (actual fighting) or exploitative competition (consumption or use).

· As the population density of one species increases, it may limit the density of the competing species as well as its own.

A. Competitive Exclusion Principle

The competitive exclusion principle predicts that two species competing for the same limiting resources cannot coexist in the same community. One will use resources more efficiently, thus reproducing more rapidly and elimination the inferior competitor.

· Derived independently by A..J. Lotka and V. Volterra who modified the logistic model of population growth to incorporate interspecific competition.

· Experiments by G.F. Gause confirmed competitive exclusion among species of Paramecium.

· Laboratory experiments have confirmed the principle for other organismis.

B. Ecological Niches

An ecological niche is the sum total of an organism’s use of biotic and abiotic resources in its environment; how it “fits into” an ecosystem.

· A fundamental niche is the resources a population is theoretically capable of using under ideal circumstances.

· Biological constraints (competition, predation, resource limitations) restrict organisms to their realized niche: the resources a population actually uses.

· Two species cannot coexist in a community if their niches are identical.

· Ecologically similar species can coexist in a community if there are one or more significant differences in their niches.

C. Evidence for Competition in Nature

If competition is as important as indicated by the competitive exclusion principle, it should be rare in natural communities, since only two outcomes are possible:

· The weaker competitor will become extinct

· One of the species will evolve to the point of using a different set of resources.

Several lines of evidence, including resource partitioning and character displacement, indicate that competition in the past has had a major role in shaping current ecological relationships.

Resource partitioning is well documented among animals.

· Sympatric species slightly different foods or use other resources in different ways. For example,

ð In the Dominican Republic, sever species of Anolis, small arboreal lizards, are sympatric.

ð They feed on small arthropods that land within their territories.

ð Each species has a characteristic perching site which reduces competition.

ð Natural selection appears to have favored perch site selection since each species has morphological characteristics (body size, leg length) which are adaptive to their microhabitats.

Character displacement is the tendency for characteristics to be more divergent in sypatric populations of two species than in allopatric populations of the same species.

· Often occurs in areas where populations of closely related species which are normally allopatric become sympatric.

· Allopatric populations of such species are similar in structure and use similar resources.

· Sympatric populations show morphological differences and use different resources.

· Two closely related species of Galapagos finches (Geospiza fuliginosa and G. fortis) have beaks of similar size when the populations are allopatric, however, on the island where they are sympatric, a significant difference in beak depth has occurred.

Indicates they feed on seeds of different sizes when sypatric.

Controlled field experiments also provide evidence for the influence of one species on the density and distribution of another species. J.H. Connell manipulated the densities of two species of barnacles that complete for attachment space in the rock intertidal zone. (See Campbell, Figure 48.12)

· Balanus balnoides is usually concentrated in the lower portions of the rocky intertidal zone.

· Chthamalus stellatus is usually found in the upper portions of the zone.

· Larvae of both settle at random and begin to develop.

· Balanus fails to survive in the upper region of the zone due to a lower tolerance to desiccation.

· Chthamalus can survive both the upper and lower regions of the zone.

· In the lower part of the zone, Balanus out competes Chthamalus for attachment sites, thus limiting it to primarily the upper part of the rocks.

VI. Commensalism and mutualism are (+ 0) interactions, respectively: a closer look

Symbiosis is a form of interspecific interaction in which a host species and a symbiont maintain a close association.

· May be parasitism, commensalisms, or mutualsim.

· All are important determinants of community structure.

A. Commensalism

Commensalism in a (+ 0) interaction in which the symbiont benefits and the host is unaffected.

o Few examples since it is unusual for one species not to be affected in some way by a close association with another species.

A good example of commensalisms is that of the cattle egret and grazing cattle. (See Campbell, Figure 48.13)

o Cattle egrets feed on insects and other small animals.

o The birds concentrate their feeding activity near grazing cattle whose movements flush prey items from the vegetation.

o The egrets benefit by an increase in feeding rates by following the cattle

o The cattle are not affected by the activity of the egrets.

Since only one species in a commensalistic association is benefited, an evolutionary change in the relationship will likely occur the beneficiary.

B. Mutualism

Mutualism is a (++) interaction requiring the evolution of adaptations in both species.

· A change in either species is likely to affect the survival and reproduction of the other.

· Examples include:

ð Nitrogen fixation by bacteria in the root nodules of legumes

ð Cellulose digestion by microorganisms in the alimentary canals of termites and ruminant mammals.

ð Photosynthesis by algae in the tissues of corals.

Mutualistic relationships may have evolved from predator-prey or host-parasite relationships.

· Some angiosperms have adaptations that attract animals for pollination or seed dispersal.

ð May represent counter-adaptations to herbivores feeding on seeds or pollen.

ð Pollen is s pared when the pollinator can feed on nectar and seeds are dispersed when animals eat fruits.

· Plants that received a benefit from sacrificing tissues other than pollen or seeds would increase their reproductive success.

VII. A community’s structure is defined by the activities and abundance of its diverse organisms

The relationships of organisms within a community are tied together in a complex web of community structure and processes.

Three features of community structure are:

· The feeding relationships among organisms.

· Patterns of abundance and diversity among species.

· The ways a community is affected by disturbances.

A. Feeding Relationships Within Communities

The various feeding relationships found within a community is the trophic structure of that community- put simply, it’s what eats what.

· Determined by predator-prey, host-parasite, and plant-herbivore interactions.

· Some interactions represent competition for food.

Community trophic structure may be studied in two ways: function groupings or food webs.

· The function groupings approach involves placing species in groups with similar trophic positions.

ð All plants are grouped together as producers; herbivores, regardless of size, are primary consumers; organisms that feed on primary consumers are secondary consumers, etc.

ð A problem arises in this method since lumping species into the functional categories may mask some aspects of the community structure.

· Food web analysis includes species-level information about the community and emphasizes species-species connections.

o Can be very complex.

o Presents a detailed knowledge of feeding relationships within the community structure.

B. Species Richness, Relative Abundance, and Diversity

Communities, even those that appear, similar, vary with regards to their species diversity.

Species diversity= The number and relative abundance of species in a biological community.

· Based on both species richness and relative abundance.

ð Species richness is the number of species in a community.

ð Relative abundance is a measure of the proportion of a species in the community as a whole.

· A community with a certain species richness with equal relative abundance of each species would have a greater diversity than a second community with the same species richness with a few common species and many rare ones.

C. Disturbances and Community Stability

Communities vary in ther responses to both natural and human-induced disturbances.

· The stability of a community is its tendency to reach and maintain an equilibrium (or relatively constant condition) in response to disturbance.

ð Depends on the type of community and nature of the disturbance.

· Community resilience is the ability of a community to persist in the face of a disturbance.

Ø Related to stability but does not imply stability of individual populations.

Ø Populations may show large fluctuations in response to a disturbance, but the community persists.

VIII. The factors that structure communities include competition, predation, and environmental patchiness.

Population interactions such as competition, predation, and environmental patchiness influence the characteristics of a community.

A. The role of Competition

Competition is recognized as an important factor in determining community structure but its importance as the major factor is open to debate.

· It is generally recognized that competition becomes more important as populations sizes approach carrying capacities ans resourves are limiting.

Many studies have documented interspecific completion, but the competition did not always result in competitive exclusion, competing species sometimes coexisted at reduced densities.

· The competition for space between barnacles discussed earlier resulted in exclusion of Chthamalus from the lower intertidal zone but it remained in the upper zone.

· Exotic species (species introduced into new communities by humans) of compete native species and alter the community structure.

B. The Role of Predation

Predation plays a complex role in helping shape community structure and may actually help maintain diversity.

· Predators do not always reduce diversity.

· A keystone predator may exert a regulating effect on other species and maintain a higher community species diversity by reducing the densities of strong competitors.

ð This would prevent competitive exclusion of poorer competitors and maintain higher community diversity.

· Defensive abilities of prey prevent them from becoming extinct.

· Prey switching also protects prey species as predators change to different prey as the population of one is depleted due to predation.

C. The Role of Environmental Patchiness

The more heterogeneous the habit, the more diverse the community.

· The greater the heterogeneity, the more ecological niches available to organisms.

· Heterogeneity may be spatial or temporal.

Spatial heterogeneity is affected by the vegetation structure in the community.

· More structurally complex vegetation provides a larger number of microhabits.

· Vegetation greatly influences the types of animals found in a community. Animal populations can more easily partition a structurally complex system than one of less complexity.

Environmental patchiness is another type of spatial heterogeneity.

· All environments are patchy over time and spaces. For example,

ð Chemical composition of rocks influences the mineral content of the soil derived from their erosion.

ð Soil moisture varies with topography.

· Environmental patchiness can increase community diversity by facilitating resource partitioning among potential competitors adapted to different local conditions.

· The importance of patchiness varies with the size and lifespan of the organisms.

Community diversity if also affected by the temporal use of habitats.

· Nocturnal animals utilize a habitat at night and are replaced by diurnal animals when it becomes day time

· A community will contain a variety of plants which bloom during different seasons.

D. Evaluating Causative Factors

Evaluating what factors are important in developing the characteristics of a community is difficult since interspecific interactions and abiotic factors that cause patchiness all have significant impact.

· Communities are structured by multiple interactions of organisms with the biotic and abiotic factors in their environment.

· Which types of interactions are most important varies from one type of community to another, and even among different components of the same community.

IX. Succession is the sequence of changes in a community after a disturbance

Ecological succession is the transition in species composition over ecological time.

· Called primary succession if it begins in areas essentially barren of life due to lack of formed soil (e.g. volcanic formations) or on rubble (e.g. retreat of glaciers).

· Called secondary succession if an existing community has been cleared by some disturbance that leaves the soil intact (e.g. abandoned agricultural fields).

· The traditional view was that in some cases, the community passes through a series of predictable transitional stages to reach a relatively stable state, the climax community.

ð Views on the validity of the climax community are changing.

A. Causes of Succession

A variety of interrelated factors determines the course of succession

· Individual species compete for available resources and replace each other.

· Different species compete better at different successional stages since resource availability changes over the course of succession.

· Early stages are typically characterized by r-selected species that are good colonizers.

ð Have a high fecundity and excellent dispersal mechanisms.

ð Others may be fugitive species that do not compete well in established communities.

· Abiotic conditions of the area, which can differ on a fairly local level, also affect succession.

The species composition during early successional stages is affected by the abiotic conditions in a barren area.

· K-selected species may colonize an area but fait to become abundant because of environmental conditions, which are outside of the tolerance limits.

· Variation in growth rates and maturation times of colonizers impact the community. For example,

ð Herbaceous species are more prevalent in early successional stages than trees because they grow faster and mature quicker.

Changes in community structure during succession may be induced by the organisms themselves.

· Direct biotic interactions include inhibition of some species by other through exploitative or interference competitions (or both).

· Organisms also affect the abiotic environment by modifying local conditions.

ð In facilitation, the group of organisms representing one successional stage “paves the way” for species typical of the next stage (e.g. alder leaves lower soil pH as they decompose, and lower soil pH facilitates the movement of spruce and hemlock into the area).

ð Sometimes facilitation for other species makes the environment unsuitable for the very species responsible for the changes.

· Inhibition and facilitation may be involved throughout the stages of succession.

At climax stage, environmental conditions are such that one set of species can continue to maintain themselves.

· Communities may never truly reach a climax, but just appear to because further change is slow.

· Many communities are also routinely disturbed by outside factors during the course of succession.

B. Natural and Human Disturbance

Disturbances are events that disrupt communities.

· They change resource availability and create opportunities for new species to become established.

· The magnitude of the disturbance’s impact depends on the size, frequency, and severity of the disturbance.

· Natural disturbances are fire, drought, wind, and moving water.

· Animals, including humans, can also cause disturbances.

Human disturbances have the greatest impact on communities.

· Logging and clearing for farmland have reduced and disconnected forests.

· Agricultural development has distrupted grasslands.

· After a community disturbance, the early stages of succession, characterized by weedy and shrubby vegetation, may persist for many years.

· Centuries of overgrazing and agricultural and agricultural disturbance have contributed to current famine in parts of Africa by turning grasslands into barren areas.

It is possible for disturbances to have positive impact on a community.

· Small-scale naturally disturbances may help maintain species diversity in a community.

ð When patches are formed during different successional stages, habitat heterogeneity is increased.

· Frequent small-scale disturbances can prevent large-scale disturbances of greater negative impact.

o Small fires prevent the accumulation of more flammable materials which would feed a more damaging large fire.

C. Community Equilibrium, Disturbance, and Species Diversity

The traditional concept of ecological succession predicts that species diversity reaches an equilibrium in the climax community.

· K-selected species (better competitors) replace r-selected species as population density increases and vegetation modifies the site.

ð The rate of species replacement would slow once the longer-lived k-selected species become established.

· Although turnover may occur, that addition of new colonists would be balanced by localized extinctions.

· Emphasizes the importance of interspecific interactions in shaping community structure.

· Interactions (predation, competition, symbiosis) become more extensive and varied, increasing diversity.

· The climax is reached when the web of interactions is so intricate that the community is saturated.

o No new species can enter unless a localized extinction occurs.

An opposing view sees communities as being in continual flux.

· The identity and numbers of species change in all successional stages, even the climax.

· Emphasizes the importance of less predictable factors (dispersal, disturbance) in shaping community compositions and structure.

· The course of succession may vary with the identity of colonizing species.

· Disturbances may prevent the community from reaching equilibrium.

· A mature community is an unpredictable mosaic of patches at different successional stages.

· Local environmental heterogeneity contributes to the mosaic structure as different species inhabit different patches.

Intermediate disturbance hypothesis states that species diversity is greatest where disturbances are moderate in frequency and severity because organisms typical of several successional stages will be present.

· Supported by studies of clearings formed by trees falling in tropical rain forests.

ð In these disturbed areas, immigrations and extinctions occur rapidly and species from different succesional stages coexist.

X. Biogeography complements community ecology in the analysis of species distribution

Biogeography= The study of the past and present distribution of individual species, as well as entire communities.

· Provides a different approach to understanding community properties by analyzing global and local phenomena.

· Traditionally concerned with the identities of species comprising particular communities.

· Currently also applies the principles of community ecology to the analysis of geographical distribution.

Terrestrial life can be divided into biogeographical realms having boundaries associated with continental drift patterns (See Campbell, Figure 48.19)

· Thus species distribution reflects past history as well as present interactions of organisms with their eonvironment

A. Limits of Species Ranges

Limitation of species to a particular range may be due to:

1. Failure of the species to disperse beyond its current range

2. Pioneer individuals that spread beyond the observed range failing to survive.

3. The species having retracted from a once larger range to its current boundaries.

The first two limitations are distinguished by transplant experiments in which specimens of a species are moved to similar environments outside of their range.

· If the transplants survive, they probably never dispersed there; if they die, it indicates an intolerance to abiotic conditions or an inability to compete limits their range.

· Most species fail to survive outside their range, but there range, but there are notable exceptions.

The third limtation is well supported by data from paleontology and historical biogeography.

· The fossil record includes evidence that close relatives of some living animals with limited ranges once had much wider ranges.

ð For example, fossils of close relatives of elephants and camels have been found in North America.

B. Global Clines in Species Diversity

The presence of clines (gradual variation) in species diversity with major geographical gradients has long been recognized.

· Generally, diversity increases in moving from far northern and southern latitudes toward the equator.

· Diversity of terrestrial organisms at a given latitude decreases with altitude.

· In the ocean benthic community, diversity increases from shallow coastal waters toward deep sea.

Many hypotheses have been proposed as to why tropical communities have such a high diversity and why latitudinal gradients exist.

1. Tropical communities are very old and rarely experience major natural disturbance. This fosters rapid and frequent speciation, and their age has allowed complex population interactions to evolve and develop to a greater extent than it temperate zones.

2. Tropical regions usually experience intermediate levels of disturbance and have greater environmental patchiness. This permits a greater diversity of plant species which forms a resource base for diverse animal communities.

3. Stability and predictability in tropical climates may permit organisms to specialize on a narrow range of resources. Small niches would reduce competition and permit a finer level of resource partitioning, both of which increases species diversity.

4. Increase solar radiation in the tropics increases the photosynthetic activity of plants. This provides a larger resource base for animals.

5. The structural complexity of tropical forests creates a great variety of microhabitats that other plants and animals can partition.

6. Diversity is self-propagating because complex predator-prey and symbiotic interactions in a diverse community prevent any populations from becoming dominant.

While most of these hypothesis will apply to some terrestrial organisms and communities, complex combinations of these factors probably operate under most circumstances.

· None of these hypotheses apply to the increased diversity of marine benthic communities with increased depth; long term stability in these habitats may explain the many relationships among these orgnamisms.

C. Island Biogeography

Islands provide opportunities to study factors affecting species diversity of communities due to their isolation and limited size.

· An island is any area surrounded by an environment not suitable for the “island” species.

· Islands can be oceanic islands or habitat islands (lakes or mountain peaks separated by lowlands).

Robert MacArthur and E.O. Wilson developed a general theory of island biogeography the predicts species diversity on an island will reach an equilibrium directly proportional to island size and inversely proportional to the island’s distance from a mainland.

· Number of species to inhabit islands is determined by immigration and extinction rates, themselves affected by island size and distance from the mainland.

· The smaller the island and the more distant from mainland, the lower the immigration rate due to difficulut in finding the island and the distance colonizers competitive exclusion.

· Immigration and extinction rates also are affected by the number of species already present.

ð As species numbers increase, immigration rate of new species decreases since new arrivals are less likely to represent a new species.

ð Extinction rate increases due to increased chance of competitive exclusion.

· Eventually, an equilibrium will be reached where immigration rates match extinction rates.

ð The number of species present at the equilibrium point being correlated to island size and distance from the mainland. (See Campbell, Figure 48.21)

· The species composition may change since equilibrium is dynamic with immigrations and extinctions continuing.

· Applies over a short period while colonization is the most important process determining species composition.

· Over longer periods, the species composition and community structure will be affected by speciation and evolutionary change in the island species.

· Theory supported from experimental research by E.E Wilson and D. Simberloff who studied small mangrove islands off the tip of South Florida.

X. Lessons from community ecology and biogeography can help us preserve biodiversity

The global support for conservation efforts has developed out of:

· Esthetic appreciation for other life forms.

· Recognition that yet undiscovered species may provide useful products

· The understanding that natural environments are necessary to maintain proper functioning of the biosphere.

· Conservation efforts are complicated by religious and cultural opposition to human population control and the economic problems facing humans in every region.

Conservation efforts currently focus on creating natural preserves which are protected from development and pollution and are designed to preserve not only endangered species but also entire ecosystems. Information from community ecology and biogeography can be applied to the preserves in order to maximize the conservation of biodiversity.

1. Preserves can be viewed as islands surrounded by disturbed habitat.

· Studies of island biogeography provide advanced knowledge about what species a preserve with a particular set of characteristics can successfully protect.

· For example, we know the number of species that can be protected in a preserve is directly related to the size of the preserve. Species in large preserves are less likely to encounter competitive exclusion. (See Campbell, Figure 48.22)

2. Detailed knowledge of species requirements is essential to preserve design.

· Minimum required sizes of preserves are known for the successful preservation of some species.

· Thomas Lovejoy used the principles of island biogeography to study “islands” of tropical rain forest left in areas of the Amazon region which have been converted to pastureland.

ð These islands range in size from 1 to 1000 hectares.

ð Teams monitor diversity at each site.

ð Diversity of small islands is decreasing most rapidly; many extinctions can be attributed to wind penetration which dessicates areas 100m or more from the edge.

ð Colonies of army ants require 10 hectares to maintain a work force.

ð In <40 hectare plots, army ants disappear first, and then five species of birds that feed on insects driven into the open by ant swarms, soon disappear.

3. Would one large preserve be more beneficial to conservation of species than several small preserves representing the same area?

· One large preserve would be preferable if the smaller preserves all contained the same species.

· Several small preserves would collectively retain a larger number of species, if the community being preserved included environmental heterogeneity resulting in different species occupying different areas.

· Several small preserves would also be less susceptible to disease epidemics which might now be able to cross unsuitable habitat.

· Spatial relationships between small preserves must also be considered. Closely species preserves or those connected by land corridors might encourage the spread of protected species among the preserves or permit recolonization by a protected species in case of local extinction in one preserve.