Ecological Principles and Ecosystem Dynamics
Ecological Principles and Ecosystem Dynamics
ECOLOGY TERMINOLOGY
Ecology is a branch of biology concerned with the study of the interactions of living
organisms with each other and with their environment.
An ecosystem is a community of organisms that interact with their environment.
Biosphere is a region of the earth where life can exist.(atmosphere, hygrosphere,
lithosphere)
A habitat is a place where an organism lives.
An abiotic factor is anything that is non-living and has an effect on living
organisms in an ecosystem. The two main types are:
1. Climatic factors are weather conditions that have an effect on living organisms in
an ecosystem.
2. Edaphic factors are anything relating to the soil or geology of land that have an
effect on living organisms in an ecosystem.
A biotic factor is anything that is living and has an effect on living organisms in an
ecosystem. (e.g presence of predator, presence of pathogenic organisms)
Pathogenic: capable of producing disease.
Symbiosis is the biological relationship in which two species live in close proximity
to each other and interact regularly in such a way as to benefit one or both of the
organisms.
(Mutualism is when both of the organisms benefit from the presence of each other,
e.g. N2-fixing bacteria that live in root nodules of legume plants (such as peas)
assimilate NO3- from N2.
Parasitism is where one organism, called the parasite, lives in or on another
organism, called the host, and the host is harmed. (e.g. aphids are parasites of plants,
athletes foot and mosquitoes)
Temporary ecosystem: it is short lived and man made or natural. Example include
rain fed pond.
Permanent ecosystem: it is long lived and self supported natural ecosystem for
very long period. Example includes forest, river etc.
(i) Producers: The role of producers is to prepare food to provide nutrition to the
other organisms present in the ecosystem. There are two types of producers;
photoautotrophs and chemotrophs.
Photoautotrophs: These are green plants which can trap sun light to form
carbohydrate, simple sugar from carbon di-oxide and water. This process is known as
photosynthesis and these organisms are called as photoautotrophs.
(ii) Consumers: These are mainly the animals. They are unable synthesize their own
food and depends on producers. They utilize the oxygen being released from the
producers as well. Several consumer doesn’t get the food from the producers but they
are depended on consumers itself. As a result, consumers are related to each other
through multiple food chains. There are many types of consumers and we will discuss
in details about these consumer in the subsequent lecture. The consumers are known
as heterotrophs.
(iii) Decomposers: These are mainly bacteria and fungi. Their primary purpose in the
ecosystem is to decompose the complex organic material into the simple inorganic
material so that it can be use for producers to prepare food.
ABIOTIC COMPONENTS
These factors include the non-living physiochemical factors of the environment.
Abiotic factors are as follows:
(i) Inorganic substances: Inorganic substances like carbon, nitrogen, oxygen, water,
carbon di-oxide, calcium, phosphorus and their inorganic compounds. These are
available as free form or dissolved in water and may be adsorbed on the soil particles.
(ii) Organic compounds: These are carbohydrates, proteins, lipids, nuceltic acids etc.
This material is present in dead organic matter. These are broken into the simple
compounds by decomposers in ecosystem for recycling of matter.
(iii) Climatic factors: These are factors present in the environment such as
temperature, humidity, light, wind, rainfall an atomospheric gaseous etc.
Study of specific Ecosystem: Lets take a example of fresh water pond to understand the
function of individual components.
1. Abiotic Components: Non-living part of the pond includes: (1) water with
dissolved gases, mineral and suspended organic matter. (2) air, CO2 and O2 on the
water surface (3) sunlight.
2. Biotic Components: The biotic constituents include the plants, animals and
microorganisms. They play different role in ecosystem.
Grazing Carnivore
Cattle mammals
mammals
Wolves
TYPES OF FOOD CHAIN: There are two different types of food chains; grazing food
chain and detritus food chain.
Grazing food chain: In the grazing food chain, solar energy is entrapped by the
plants and then biomass, in tuen eaten by the herbivorous, and these are
subsequently been consumed by a variety of carnivorous. These are longer food and
these food chains end at the decomposer level. Here are two typical example of this
type of food chain to understand this type of food chain.
(1) Food chain in a pond: In a pond, floated or rooted plants and algae are responsible for
performing photosynthesis to prepare food for other member of ecosystem. They represent
producers in the food chain (Figure 39.2). Unicellular algae are consumed by protozoan, water flies,
snail, mosquito larvae and tadpoles. These small organisms represent primary consumers. These
organisms are eaten by hydra, dragonfly larvae, giant insects and small fishes. These are secondary
consumers. Large fishes and frog fed on these organism and represent tertiary consumers. Frog and
fishes are eaten by snakes, birds and these are quaternary consumers. Death of all these organism
become the food for bacteria and fungus to produce simple inorganic materials for reuse by the
producers.
(2) Food chain on land: A typical land food chain is given in Figure 39.3. In land food chain, grass
and tree are the producers. Grass is eaten by rabbit and other herbivorous. They represent the
primary consumers. Rabbit is eaten by cats (secondary consumers), which in-turn eaten by wolves
(tertiary consumers). Both cat and wolves will be consumed by tigers and other big carnivorous
(quaternary consumers). Deaths of these entire organisms become the food for bacteria and fungus
to produce simple inorganic materials for reuse by the producers.
Detritus food chain: Unlike grazing food chain, detritus food chain starts with the dead organic
matter either from fallen leaves or dead animal bodies. This food chain doen’t depends on solar
energy. Common example of detritus food chain is marsh land where mangrove leaves fall into the
warm, shallow water (Figure 39.4). The detritus eating animals ex. Bacteria, fungi and protozoan act
upon the dead matter of dead leaves to covert them into simple inorganic substances. The
detritivorous are subsequently eaten by insect larvae, grass shrimp, copepods, crabs, nematodes,
bivalve mollusks, amphipods, mysids etc. In the last step, the detritus consumers are finally eaten by
fishes.
Food Web: The different food chains are inter connected at various trophic level to develop a food
web (Figure 39.5). For example, in grassland ecosystem, grass is consumed by the rabbit but in their
absence, it may be eaten by the grazing cattle. Similarly, rat or mouse is eaten by snake but snake can
be eaten by predatory birds. In contrast to food chain, food web has several distinct characteristic.
(1) Food web are never straight. (2) Food web is formed due to interlinking of food chains. (3) A food
web in the ecosystem brings alternate source of food. The complex food web gives better stability to
the ecosystem. Most of the animals are polyphagous and they feed on more than one kind of
organism. If the availability of one particular animal is decresing in the ecosystem, they start eating
alternate animal. As a result, it gives chance to other animal to reproduce and grow in number and in
addition, it gives chance to predator to survive.
Ecological Pyramids: In a food chain, producers and consumers at different trophic level are
connected in terms of number, biomass and energy. These properties reduces from producers to
consumers and representing these parameters for food chain gives a pyramid with a broad base and
a tapering apex (Figure 39.6). Ecological pyramids can be of three types:
POPULATION ECOLOGY
I. Background
A. Biological processes affecting populations
1. Population ecology is the study of populations in relation to environment
a. Environment influences population density, distribution and size
2. Definition of population
a. A group of individuals of a single species living in the same general area
C. Density
1. Usually impractical / impossible to count all individuals in a population
a. Need to employ sampling techniques to estimate densities and total population sizes
2. Techniques
a. Extrapolation from small samples
b. Index of population size
c. Mark-recapture method
3. Factors affecting density
a. Processes that add individuals to some population & remove individuals
b. Immigration
i. Influx of new individuals from other areas
c. Emigration
i. Movement of individuals outof a population
4. Environmentaland socialfactors influence spacing of individuals ina population
a. Clumped dispersion
i. Individuals aggregate in patches
ii. Clumped dispersion influenced by resource availability and behavior
b. Uniform dispersion
i. Individuals are evenly distributed
ii. Influenced by social interactions such as territoriality
c. Random dispersion
i. Position of each individual is independent of other individuals
ii. Occurs in absence of strong attractions or repulsions
D. Demogra
phics
1. The
study of
the vital
statistics of a population and how they change over time a. Death and birth ratesLife table
a. Age-specific summary of the survival pattern of a population
b. Follow cohort of the same aged individuals
E. Survivorship curve
F. Reproductive rates
1. Focus on females when a population reproduces sexually
2. Reproductive table
a. Age-specific summary of the reproductive rates in a population
b. Describes reproductive pattern
II. Life history traits
A. Traits that affect its schedule of reproduction and survival
1. Age when reproduction begins
2. Frequency of reproduction
3. Number of offspring during each reproductive cycle
4. Life history traits are evolutionary outcomes reflected in the development, physiology, and
behavior of an organism
B. Types of life histories
1. Semelparity (big-bang reproduction) organisms reproduce once and die
a. Favored when environment is unpredictable
2. Iteroparity, or (repeated reproduction) organisms produce offspring repeatedly
b. Favored when environment is consistent
C. Limited resources lead to trade-offs between survival and reproduction
1. Plant strategies
a. Large number of small seeds
i. Some will grow and reproduce
b. Small number of large seeds
B. Exponential growth
1. Exponential population growth is population increase under idealized conditions
Under these conditions, the rate of reproduction is at its maximum, called the intrinsic rate of
increase
[Link] capacity (K) is the maximum population size the environment can support
B. Logistic growth model
1. In the logistic population growth model, the per capita rate of increase declines as
carrying capacity is reached
a. As a prey population builds up, predators may feed preferentially on that species
7. Intrinsic factors
a. Complex interactions between biotic and abiotic factors that cause variation in
population size
9. Stability and fluctuation
a. Long-term population studies have challenged the hypothesis that
populations of large mammals are relatively stable over time
b. Weather can affect population size over time
c. Changes in predation pressure can drive population fluctuations
1. Human population increased relatively slowly until about 1650 and then began to grow
exponentially
2. Global population is still growing, the rate of growth began to slow during the 1960s
B. Regional patterns of population change
1. To maintain population stability, a regional human population can exist in one of two
configurations:
a. Zero population growth = High birth rate – High death rate
b. Zero population growth = Low birth rate – Low death rate
2. Demographic transition is the move from the first state toward the second state
a. Associated with increase in quality of health care and access to education
i. Greatest effect if for women
3. Most of the current global population growth is concentrated in developing countries
C. Age structure
1. Age structure is the relative number of individuals at each age
2. Age structure diagrams can predict a population’s growth trends
E. Global carrying capacity
1. The number of humans that the biosphere can support
a. The carrying capacity of Earth for humans is uncertain
b. Average estimate is 10–15 billion
2. Limits
a. Ecological footprint concept summarizes the aggregate land and water area needed to
sustain the people of a nation
b. Measures how close we are to the carrying capacity of Earth
c. Countries vary greatly in footprint size and available ecological capacity
d. Carrying capacity could potentially be limited by food, space, nonrenewable resources, or
buildup of wastes.
ECOLOGY
Population Ecology
In unitary populations, each individual is derived from zygote (the product of fertilization
of male and female gamete) and the growth of such individuals is determinate and
predictable. Examples include mammals (including humans), birds, amphibians and
insects. Each cow has four legs, two eyes, and a tail., i.e., each individual shows a definite
shape and size (Photo 2a).
In contrast, modular populations are those where an organism develops from a zygote and
serves as a unit module and several other modules are produced from it, forming a
Photo 2a. Unitary Population of Photo 2b. A Grass showing different Ramets
Cow
branching pattern (Photo 2b).
Examples of modular organisms are plants, sponges, hydroids, fungi, bacteria and corals.
Some modular organisms such as trees may grow vertically while others like grasses
spread horizontally on the substratum. The structure and pattern of modular organisms is
not determinate and thus unpredictable.
Biologists also use the term Genet to the organism, which arises from a zygote, whereas
others arising asexually are known as Ramet. In a grass or weed species, a number of
young plants may arise through runners or stolons, and upon separation from the parent
plant form new plants; a group of such new plants is known as ramets (Photo 2b).
Individuals of ramets are genetically alike and replica of parent plant. A group of ramets
developing from a genet is known as clone since all organisms are genetically alike. The
formation of ramets in the plant species is very common and can be easily seen in grasses.
The subject of population ecology can be divided into 3 sections for the sake of
convenience:
A) Population characteristics
B) Population dynamics
C) Population regulation
A. Population Characteristics
Populations are identified by a number of characteristics. These are: 1. Population size and
density, 2. Patterns of dispersion, 3. Age structure, 4. Natality, 5. Mortality, 6. Population
growth and dispersal, 7. Biotic potential.
Population size is usually determined on the basis of density, i.e. number of individuals per
unit area (if it is land) or per unit volume (if it is an aquatic system). For example, 200 trees
found in one hectare of land tell us about the density of the tree population, or 15
fishes/m3 water indicates the density of fish population. Density of the population is often
of two types - Crude density and Ecological density.
> Crude density is that density which takes in account all area of land or aquatic
ecosystems under consideration, e.g. number of squirrels in a forest.
> Ecological density on the other hand, takes in account abundance of individuals in
the actual area occupied by a population. If we consider the above example of
squirrels, numbers of squirrels per unit area of the tree dominated patches (areas
where squirrels are actually living) constitute ecological density.
The difference in the two types of densities becomes more apparent when the species are
clumped together in a small area. However, crude density is studied frequently more than
the ecological density because it is very difficult to determine the ‘actual area’ of
inhabitation of a species. Further, the area of inhabitation may vary with developmental
stages of species.
2. Patterns of dispersion
Clumped dispersion: In this type of pattern, the individuals of a species are clumped
together in space in the form of patches (Figure 1). This type of patchy distribution is quite
common in nature as individuals of a population occur together because of food
availability or better survival rate as in animal populations. In plants, the clumped
distribution is very common, and attributed to nutrient availability, specific habitat
preference or better environmental conditions. Example of this kind can also be seen in the
A population is comprised of individuals of different age groups that constitute its age
structure. Age structure of a population thus derives from the proportion of individuals in
different age groups. For the sake of convenience, the age categories have been divided
into three major stages, Pre-reproductive, Reproductive and Postreproductive. The
proportion of different stages in a population is presented graphically in the form of age
pyramid. An age pyramid is thus a geometrical model showing the proportions of different
age groups of a population. Populations with equal proportion of major three stages are
said to be stationary populations (Figure 2a). A population with high number of young
individuals as compared to the older organisms is increasing or progressive type and the
pyramid of such a population would have a broader base (Figure 2b). On the other hand, if
the number of older organisms is more than the younger ones, the population is said to be
retrogressive or declining type. The base of the pyramid of such population would be
narrow (Figure 2c).
4. Natality
Maximum or Absolute natality also known as Fecundity rate means maximum offspring
produced under most suitable environmental conditions. This value is theoretical (since
the environmental conditions are never static and keep on changing) and constant for a
given population.
Ecological natality also known as Fertility rate, on the other hand, refers to number of
offspring produced under prevailing environmental conditions.
5. Mortality
Minimum mortality rate, or also known as Physiological longevity, refers to the theoretical
minimum death rate which occurs under ideal conditions of environment with minimum
limiting factors. This value is a theoretical value and constant for a given population. Under
actual environmental conditions, the death rate may be more and this actual death rate is
referred to as Ecological mortality.
The other way of expressing mortality is vital index, which is ratio of birth to death rate
and expressed as percentage.
The most popular way to express mortality in a population is to prepare a survivorship
curve. A survivorship curve for a given population is a graph drawn between numbers of
survivors (on a log scale) on Y-axis against age on the X-axis. In general, there are three
patterns of survivorship curves (Figure 3).
Type 1 - It is also known as highly convex curve. It reflects higher rate of survival or low
rate of mortality of younger individuals as compared to the older ones. This type of curve is
found in human beings.
Type 2 - This curve shows a steady death of individuals per unit time throughout the life,
and is found in some reptiles, corals, honeybees and rodents. This shows a straight-line
relationship between age and number of survivors.
Type 3 - This is also known as highly concave curve. It shows higher mortality of
individuals at young stage as compared to old stage. It is found in plants, sea urchins and
fish species.
Age
birth (b) and death (d) of individuals also change population size. Immigration and birth
increase population size whereas emigration and death decrease its size. Thus, in a given
population if birth + immigration > emigration + death, the size of population would
increase. On the other hand, if the birth + immigration < emigration + death, then the size
of the population would decrease.
7. Biotic potential
B. Population Dynamics
Populations are never static and keep changing in time and space. These changes in
population size over time show varied trends. When environment is unlimited (adequate
space and food supply) the specific growth rate (population growth rate per individual) of
populations becomes maximum and constant under a set of environmental conditions. On
the other hand, if the food supply or other resources are limited, the growth rate is
typically sigmoid, i.e. increases slowly in the beginning followed by rapid increase and then
becomes constant as it approaches the upper limit. To address these growth patterns,
there are two types of growth models These are:
a. J-shaped or Exponential Growth Model
b. S-shaped or Sigmoid or Logistic Growth Model
When population growth occurs at a place where resources are limited, it attains a
sigmoid or S-shaped curve showing minimum death during early stages. The population
increases in size until it reaches an upper limit. This upper limit is known as the Carrying
capacity, which is denoted by ‘K’. Carrying capacity thus may be defined as capacity of an
ecosystem to support maximum number of individuals of a species. As the population size
increases, population growth rate declines as it approaches carrying capacity. Sigmoid
growth is thus density dependent and can be expressed by the following equation:
W.C. Allee, an ecologist known for his extensive research on social behaviour of animals,
gave a concept known as Allee’s principle. Allee’s prinicple is a relationship between
population density and survival of animals. According to Allee, both under-crowding (low
population density) and over-crowding (high population density) limit growth and survival
of a population. There are a number of examples (in both plants and animals) where Allee’s
principle holds good. A number of plant species occur in groups, which may be in response
to habitat preference or suitable climatic or environmental conditions or due to
reproductive strategies. Within a group, the survival rates of species increase in response
to the adverse environmental conditions. For example, species of Polygonum pleibium
prefers to grow in clayey soil and often form groups or patches. Likewise, populations of
Stellaria media or Anagallis arvensis form patches owing to their preference for better
moisture conditions. Some species form groups or patches due to vegetative reproduction
or due to lack of effective seed dispersal mechanism. Survival chances and fitness of such
species is best at moderate populations. As the population density increases beyond limit,
there is competition for resources, and it is detrimental to growth and survival of such
species. The Allee’s Principle is also valid in animal populations. There are a number of
social insects, termites, ants, which survive and grow best at moderate densities and are
able to overcome harsh conditions. Bees and colonial bird are the best examples of group
survival. Allee’s principle is also very relevant to human beings who form social
aggregations particularly in the urban environment.
C. Population Regulation
A number of factors like availability of food, space, water, and pests may regulate
population size. In general, the factors responsible for population regulation can be
density dependent (competition, predation, parasitism, disease outbreak, or herbivory) or
density independent (environmental factors). In density dependent factors, competition
(particularly intra-specific i.e. between individuals of same species) plays a major role in
limiting population size. Among the density independent factors, floods, fire and other
natural calamities remove large proportion of the populations and thus decrease their
density.
Sometimes individuals of a population release toxic substances in the soil or water, which
tend to limit the growth of their own type of plants (consepecifics) and thus control over-
crowding of a species at a particular place. This is known as autoallelopathy or
autotoxicity - a type of interaction where one species releases toxic substances into
environment that are detrimental to individualists own growth. Autotoxicity is well
demonstrated in a number of food plants like alfalfa (Medicago sativa), figs (Ficus species),
grape (Vitis vinifera) and peach (Prunus persica) orchards; in aquatic and wetland plants
like Typha, Phragmites, Juncus and algae; and in forest tree or shrub species like Casuarina,
Walnut (Juglans species), Coffee (Coffea arabica) and tea (Camellia sinensis),
Community Ecology
Each community has spatial limits or boundaries. The boundaries between communities
may be very sharp such as boundary between a forest and a lake or less sharp, e.g.
boundary between two types of forests or a forest and a grassland community. Often there
is some transitional area between two communities that is knows as Ecotone where species
of both adjacent communities are found. The ecotonal communities are rich in species
diversity because of the edge effect (contrasting environmental conditions at the
boundaries or the edges supporting a high species richness). For instance, a patch of land
between two forest communities will have animals and plants common to both the forest
communities.
Characteristics of Communities
There are various characteristics of communities such as species diversity, structure and
composition, dominance, succession (or developmental history) and trophic structure.
Each one of these is discussed as under:
Species diversity can be measured by using various diversity indices - the mathematical
expressions based on species abundance data. Species diversity can be measured
separately either as species richness or evenness or diversity as a whole. Species richness is
measured by Index of richness (denoted by R in the formulae given in Box 1) given by
Margalef (1958). Species evenness can be measured with evenness index (denoted by E)
given by Hill (1973). Diversity of the species can also be calculated directly with a variety of
indices, of which twocommonly used are Shannon-Weiner Index or simply the Index of
diversity or Shannon’s index (denoted by H'; as given by Shannon and Weaver, 1963) and
Index of dominance (or X) or Simpson’s index given by Simpson (1949) (See Box 1).
Shannon‘s index has a direct relationship with the species diversity, whereas index of
dominance has an inverse relationship. The formulae for calculating various species
diversity indices are given in the Box 1.
For a community to be stable, it requires two components - Resilience and Resistance.
Resilience is the ability of a community to recover after facing a disturbance or
displacement. Resistance, on the other hand, is the ability of a community to avoid
disturbance (any event that alters structure of a community) or displacement (shifting of
the community to some other place). One of the reasons for the species rich complex
communities acquiring stability is that any change in one or a few species would be
compensated by the other species. Some other studies, however, have indicated that
greater complexity in a community leads to instability. Thus, it remains controversial
whether complexity of a community leads to stability or unstable conditions. However,
ecologists have successfully found a relationship between competition and diversity or
stability. If the competition is severe, there is low diversity because only those species
survive what are able to withstand harsh conditions by suitably adapting themselves. On
the other hand, if the competition is weak and the requirements of species do not overlap,
the species will not fight for resources and thus more and more species can coexist. The
competition becomes intense if the resources for the life support system - food, air, water,
space, sunlight (in case of plants, especially) are scarce and the requirements of the species
overlap.
Each community has its own structure and composition. For instance, the community of
rain forests in silent valley will be different from that of rain forests in Arunachal Pradesh.
Community structure is often expressed in terms of its major growth form such as trees in
forests or grasses in grasslands. The arrangement of different growth forms determines the
structural pattern of the community. In a community, spatial arrangement of the
components is also very important. For example, in a forest, some plants may be shade
loving and confined to understorey while others are adapted to intense sunlight like
emergent trees.
Still other plants need better soil-moisture and some may grow in dry stony areas.
Likewise, in a pond ecosystem the plants that need soil will remain confined to the edges of
pond, while the free-floating will cover the water surface. This horizontal distribution of a
community is known as zonation.
In aquatic bodies, particularly lakes and ponds, three different types of zones differentiated
on the basis of light availability and depth of water are very common such as Littoral zone,
Limnetic zone and Profundal zone (Figure 7). Each of these zones supports distinct
community.
Limnetic zone is the open free surface of ponds and lakes up to which light penetrates.
Since this zone of water is fully illuminated, photosynthetic (autotrophic) organisms like
green algae, blue green algae and even free-floating or submerged higher plants occupy it.
These organisms are typically adapted for floating or swimming. These can be planktons
(organisms that are able to float), nektons (organisms that are able to swim and navigate)
and also neustons (organisms that rest or swim on the surface). The level of water upto
which light penetrates is known as Light Compensation Point.
Profundal zone, on the other hand, is the deep-water zone of the ponds and lakes beyond
light compensation level where heterotrophic (non-photosynthetic) organisms live. The
organisms of this zone are dependent on Limnetic zone for food and in return replenish
nutrients.
In some ponds and lakes there is little distinction between littoral and Limnetic zone and in
such cases the upper surface of water up to light penetration point is known as Euphotic
zone.
The pond water can also be divided into Epilimnion and Hypolimnion based on
temperature differences. In between the two layers there is an intermediate zone known as
Thermocline (Figure 8). This type of distinction is very common in temperate lakes,
wherein during the summer season the top water layers become warmercompared to the
lower layers. As a result, the water circulates only in the top warmer layers and does not
mix with the lower colder water layers. This creates a sharp temperature gradient
separating upper circulating warmer layers known as Epilimnion from lower non-
circulating colder layers known as Hypolimnion. In between Epilimnion and Hypolimnion
The forest communities are highly stratified (forming distinct vertical storeys). In a typical
forest, there are five different vertical storey viz. subterranean part (deep in soil), forest
floor, herbaceous vegetation, shrubs, and trees. In contrast, grasslands show poor vertical
stratification. It has only two layers - a subterranean part with roots and rhizomes and
herbaceous part consisting of grasses, herbs and weeds.
Trophic structure of a forest community also has a same pattern but with different species
composition. In a forest, the autotrophs or the producers are the trees, which are also the dominant
species. Additionally, the forests also have shrubs, herbs and grasses that are autotrophic and form
a distinct understorey, but their role is lesser than that of trees. The type of the trees in the forests
varies from place to place depending upon environmental conditions.
For example, a typical tropical moist deciduous forest is composed of tree species like teak
(Tectona grandis), sal (Shorea robusta) or Queen’s myrtle (Lagerstoemia parviflora);
whereas a temperate deciduous forest has trees like oak (Quercus), maple (Acer sp.), birch
(Betula sp.) and spruce (Picea sp.). The primary consumers in the forests include ants,
beetles, leafhoppers, spider and bugs that feed on tree leaves. Besides, there are larger
animals like elephants, nilgai, squirrels, rabbits, flying foxes and birds, which feed on shoots
or fruits of the trees Birds, snakes, lizards and foxes constitute secondary consumers
whereas lions and tigers constitute tertiary consumers., The decomposers include several
types of fungi, bacteria and actinomycetes.
Succession: Succession is the orderly process of community development and refers to the
continuous, unidirectional and sequential change in the species composition of a given
community over time. It involves various stages during which a specific set of species
occupy the area and replaced by the next group of species. All these stages of succession
are known as seral stages. The first stage of succession when the bare area is colonized for
the first time is known as Pioneer stage and such species are referred to as Pioneer species.
The final, mature, stable and long lasting community is known as Climax community.
Plant communities can be studied by different methods such as floristic (by simply
studying various genera and species) and physiognomic (based on Raunkiaer’s life forms)
and phyto-social methods. Of these, phyto-social methods are preferred. In these, the data
on the vegetation is collected in terms of types of species present and individual number of
each type in an area. As the areas are very large, it is not possible to count every plant, thus
the area is divided into smaller units known as sampling units. Three types of sampling
units are generally considered for studying various plant communities. These are: a) Area,
b) Line, and c) Point. Area and line both are based on definite size of the sampling unit
while point is used in those situations where it is difficult to determine area e.g. thick
forest. Sampling unit where definite area is selected is known as Quadrat. Quadrat is thus a
sampling unit of definite area that is usually a square but it can also be a rectangle or circle.
Size and number of quadrats are determined based on the objective and features of area
under consideration. Depending upon the purpose of study, the quadrat may be list
quadrat (where species present in the area are listed), list-count quadrat (where species
are listed as well as their numbers counted), chart quadrat (where all details like
distribution of species, their number are recorded on a graph paper periodically using an
instrument pantograph) and permanent quadrat (used in the experimental studies where
vegetation is recorded for a long time to find out changes). Transect is the term used in
cases where sampling unit is a strip of definite area. Transect may be a line or belt
depending upon the study area. In a line transect, sampling is usually done across a line. In
belt transect, an area (belt) of suitable size is selected where the sampling is done. Belt
transects are particularly used in forests and can be further divided into segments for
convenience.
For determining quadrat size, species-area curve method is used. Sampling unit size is
increased gradually (starting from a minimum) and the number of types of species counted
in each sampling unit. It is continued until number of species become constant for three
consecutive times. Then, a graph is drawn between area (X-axis) and number of species (Y-
axis) and from the curve so obtained, optimum size of quadrat (where the number of
Point is used as a sampling unit in areas where determination of suitable area is not
possible with quadrats e.g. in thick forests and large grasslands. For this, a number of
movable pins (usually 10) are inserted in a wooden frame at 45° angle is known as Point
frame. Point frame is laid randomly in an area, plants hit by the pins are recorded, and their
frequency determined.
Community Features
Quantitative characters: Quantitative characters are those that can be measured, e.g.
density, abundance, frequency, cover area and basal area of species present in a given area.
These values can be expressed as absolute or as relative values. Density and Abundance:
Density of a species reflects the numerical strength of species in a given community.
For more clarity see example in Table 1 where density of five species has been shown as
calculated by the above formula. Another important aspect about density is that if the size
of the quadrat is either lesser or more than 1m 2, the final value of density is presented
equivalent to 1m2. This is true only in grasslands or communities of a smaller area, but not
in forests or aquatic systems.
Density can also be presented as relative density. Relative density is calculated based on
following formula:
Note: Since the relative value of density is less than 1.0. It can thus be converted into
percent by multiplying with 100.
From the above example (Table 1), the relative density for species 1 is calculated by taking
its individual density
i. e. 30 and dividing it by 137, i.e. total densities of all species. To convert it into
percent relative density, multiply it with 100. It comes out to be 21.80%. Likewise, the
relative density of other species can be calculated.
Abundance is also calculated like density but in this case, only those quadrats are
considered for calculation where a species actually occurs. For example, if a species has
occurred in only 3 quadrats out of total 5 studied, then the total number of individuals of
the species is divided by 3 (instead of 5, as in case of density). The difference between
Abundance is also presented on the basis of unit area, i.e. 1m 2 especially in smaller areas or
grasslands. However, it is not much used as compared to density in ecological studies.
distribution or dispersion of a species in a given area, and given in percent. For example, a
species is distributed uniformly in an area there is greater probability of its occurrence in
all quadrats and it would have maximum frequency. In another case, a species may be
clustered or present only in a part of the area. In this case, it will occur only in few quadrats
and hence it would have lesser frequency. The frequency of a species in a given area is
studied by either quadrat method or transects and is calculated by the following formula:
Thus, if a species occurs in 5 out of total 10 quadrats studied, its frequency would be 50%.
If a species occurs in all the quadrats studied, its frequency would be 100%. The frequency
determination also becomes clear from Table 1.
Further, Raunkiaer suggested Law of frequency and Normal Frequency Diagram based on
the data from his studies in all the natural ecosystems. According to law of frequency,
species poorly distributed or dispersed in an area are likely to be presented more
compared to those that have better or more dispersion in an area. In other words, A>B>C>
= <D<E, i.e. A is greater than B, which is greater than C, and C may be greater or equal or
lesser than D, which in turn is lesser than E. Raunkiaer’s normal frequency diagram was a
histogram made on the basis of the average frequency data in which value of class A was
53%, that of B 14%, C 9%, D 8% and E 16%. Raunkiaer also prepared a normal frequency
diagram, a ./-shaped curve, which represents homo- or hetero-geneity of a community. It is
a /-shaped curve. After the preposition of Law of frequency, a number of studies were
undertaken in various parts of the world and similar observations were obtained especially
in the natural and undisturbed ecosystems. In disturbed ecosystems, however, the
frequency distribution varies from that of normal as proposed by Raunkiaer.
Like density, frequency can be expressed in relative terms. For this, sum of frequencies of
all species is calculated and following formula is applied:
This can also be converted into percent relative frequency by multiplying with 100. The
relative value is important in further determining importance value index of species, which
gives the total ecological status of species.
Basal Area and Dominance. Cover area, also known as herbage area, is usually confined to
above-ground parts and is defined as percent area occupied by the above ground parts of
species per unit area. It tells us about the dominance of a species in terms of area occupied
by its aerial parts in given vegetation. Basal area is calculated from the point of ground
where the stem of the plants pierces out of the ground. At this junction, i.e. near the ground,
the diameter of the stem is measured with scales, calipers, or screw gauge. Based on
formula for any area measurement i.e. nr2, the basal area of each species is calculated.
Normally for a species, basal area of a large number of its individuals is determined and
then the average value is calculated. This average value is then multiplied by density value
of that species which gives the value of basal area per square meter, also known as
dominance.
For dominance also, relative value is calculated as per the following formula.
This can also be converted into percent relative dominance by multiplying with 100. In
case of trees, circumference of trees is measured at breast height (1.5m from base). From
circumference, the radius is calculated and in turn from radius, area is calculated. In trees,
the crown area is calculated based on area of its crown that is measured by taking radius
along crown perimeter on the ground surface starting from the stem of the tree. If the
crown of the tree is not circular which is normally so, then several values of radii are
measured across different lines and then average radius is calculated. Area is then
calculated by simple formula, i.e. nr2.
Phenology. It refers to the periodic occurrence of different events in the life cycle of a
species. It means when does a species germinates, grows vegetatively, flowers and
produces seeds, and how and when disperses the seeds. All this information about a
species is determined periodically and presented in the form of a phenogram. A phenogram
is simple hexagonal structure presenting different events in the life of a species, e.g. the six
arms of phenogram show period of germination, vegetative growth, flowering time, fruit
formation, seed maturation and death of the species. In a community, each species has its
own phenology and this reflects a great diversity.
Physiognomy: Physiognomy refers the outer appearance of a community and is an
important parameter that tells us about the structure of community. It is based on the
growth form of its dominant species. For example, a grassland community is dominated by
grasses, forests by trees and chaparral community by shrubs.
Life Forms:Life forms better known as Raunkiaer ’s life forms or Botanical Life Forms were
proposed in 1934 by a Danish botanist Christen C. Raunkiaer. According to Raunkiaer, in a
community it is very important to know how a plant survives during unfavourable
conditions. He took the criterion of protection of perennating buds during adverse
conditions as an adaptation of plant to climate. Accordingly he proposed a system known
as Raunkiaer’s system in which plants were categorized into various life forms based on
the position of their buds during seasons of unfavourable conditions (too much cold or too
much hot). Raunkiaer considered five major types of life forms viz. Phanerophytes,
Chamaephytes, Hemicryptophytes, Cryptophytes, and Therophytes.
1. Phanerophytes (Phanero - visible; phytes - plants; plants where buds are visible): These
are those plants whose buds are situated high up on the plant on the top of the shoots.
These are either naked or covered with scales. Phanerophytes are very common in tropical
areas and their number decreases towards temperate and polar areas. Based on the height
of trees, phanerophytes are further divided into 4 categories:
a) Mega-phanerophytes - trees taller than 30 m
b) Meso-phanerophytes - trees between 8 - 30 m
c) Micro-phanerophytes - trees between 2 - 8 m height
d) Nano-phanerophytes - shrubs shorter than 2 m but more than 25 cm
2. Chamaephytes:These are those plants whose buds are close to ground or maximum up
to 25 cm. These plants are found in colder regions at high altitudes or latitudes, e.g.
Temperate America. During the growing season, sometimes the aerial parts of
chamaephytes die and cover the buds. Fresh growth occurs during the onset of favourable
season.
3. Hemicryptophytes:These are also found in the cold regions where buds remain
covered under surface soil (but not deep-seated), and are protected. These include annual
(plants which complete their life cycle in one year or one season) or biennial (which
complete their life cycle in 2 years or 2 seasons) herbs.
4. Cryptophytes:These are also known as Geophytes. In these plants, the buds remain
buried under soil such as bulbs and rhizomes. Such plants are mostly found in the arid
regions of the world.
5. Therophytes:These are the ephemerals or seasonal plants that complete their life cycle
quickly under favourable conditions and during the rest of the unfavourable conditions
remain in the form of seeds.
Besides these five major categories, Raunkiaer also identified epiphytes (plant growing on
or attached to other plants) as a separate category of life forms. Additionally, he also
divided cryprophytes into three subtypes: geophytes (plants buried in soil with
subterranean or perennating buds), hydrophytes (plants submerged or floating in aquatic
systems with perennating buds inside water), and halophytes (plants in marshy swampy
areas with high salt concentrations).
Biological Spectrum: It refers to the relative percentage of species of different life forms
in a given community is and is also known as Phyto-climatic Spectrum. Thus for
preparing a biological spectrum percentage of each of the 5 life forms is calculated.
Raunkiaer (1934) also prepared a normal biological spectrum of flora of the world based
on his elaborative and extensive ecological studies. For the normal biological spectrum, the
percent values of different life form are given (Table 3).
The biological spectrum obtained for any area is compared with normal biological
spectrum that reflects the variations or deviations from the normal. It is generally thought
that biological spectrum of a region reflects its environmental or the climatic conditions.
For example, higher ratio of phanerophytes in an area indicates tropical conditions and
those of chamaephytes reflect extreme cold conditions. Thus, it has been suggested as an
indicator of climatic condition of an area. However, its utility is limited since biological
spectrum is disturbed when the environmental conditions fluctuate. Further, biotic stress
also affects the biological spectrum of an area that too limits its use.
Environmental conditions exhibit great fluctuations. Plant species have to tolerate these
variations in the environmental conditions, which may be reflected in terms of different
climatic conditions, habitats, edaphic conditions or even different geographic areas. The
survival of species in such conditions is dependent upon its ecological amplitude - the
extent to which a species may tolerate environmental variations. Species with a wider
ecological amplitude have better adaptability and vice versa. The response of a species to a
particular environmental condition may be reflected through several morphological
variations (changes in the external appearance, i.e. in terms of height, number and size of
leaves, number of branches, number of flowers produced, size of flowers and seed output).
Thus, even within a species several morphological races or forms may be encountered.
Swedish gene ecologist G. Turesson first gave this concept (occurrence of morphological
races of a species) in 1922 and 1930. He stated that variations within species go hand in
hand with environmental variations. For example, individuals of a species growing at
higher altitude may be dwarf or short in height in comparison to those growing in plain
areas. A number of differences in morphology of a species can be seen in response to
different habitat or climatic conditions. Often these variations may become genotypic or
inheritable i.e. transferred from one generation to the other. In other words, these
variations become genetically fixed. Such morphological races where variations in their
external appearance are transferred from one generation to the other are known as
Ecotypes. Ecotypes thus are those individuals of a species that vary in external appearance
and their variations are genetically fixed and irreversible. Other names for ecotypes are
ecological or physiological races. If such ecotypes are brought under similar
environmental conditions, differences between them persist since these are genetically
fixed. However, these are merely ecological races and cannot be given the rank of new
species since these are inter-fertile (these individuals can breed together or reproduce).
For example, Euphorbia hirta, known as Lal dudhi in Hindi, has two ecotypes: Ecotype 1 is
erect type growing in moist areas. Ecotype 2 is a prostrate type that grows in dry
conditions. Likewise, ecotypes have been reported in a number of plants in response to
climatic, edaphic and even biotic conditions.
Ecological Succession
Plant communities keep changing with time and space. These changes in the communities
may either be due to changing environmental conditions or communities themselves such
as their mutual interactions. Thus, in an area, one community may replace the other, and in
turn, may be got replaced by another community. This change in community structure and
composition over a period until there is a formation of a stable community is known as
Ecological succession. Ecological succession has also been termed as Ecosystem
development by some ecologists. It is predictable and orderly process. The final stable
community formed at the end of succession exists for a longer period and is in harmony
with the existing environmental conditions. This final stable community is known as
Climax community, whereas the communities that appear for a shorter time, and are
replaced in succession are termed as Seral communities or Seral stages. The plant
community that colonizes an area for the first time is termed as Pioneer community and
such plants as Pioneers or Primary colonizers.
Types of Succession
Primary and Secondary Succession: If the succession starts from the primary
substratum free of any living or organic matter (unoccupied habitat), it is termed as
primary succession. It may occur in terrestrial (land) or aquatic (in water) ecosystems and
is slow in nature. Secondary succession, on the other hand starts from already build-up
substratum. In such areas, plant community earlier occupying the area get altered due to
disturbances like sudden changes in climate, fire, floods or some biotic interference. The
succession starting from such a substratum is termed as secondary succession and it is
comparatively rapid.
Autogenic and Allogenic Succession: During the process of succession, the mutual
interactions among the living organisms of the community change the environment. These
changes make the environment unfavorable for the existing community and thus cause its
replacement. However, such changes may be congenial for some other community. This
type of succession where the community replacement occurs due to reasons created by
community itself is known as Autogenic succession. If during the succession, the
replacement of one community by the other may be caused by environmental factors and
not by living organisms, then the succession is termed as Allogenic succession.
Autotrophic and Heterotrophic Succession: A succession in which green plants or the
autotrophs dominate, so that there is a continuous energy flow during the whole process, is
known as Autotrophic succession. In contrast, succession wherein heterotrophs such as
bacteria, fungi, actinomycetes or even animals dominate and there is a continuous decline
in the energy flow is known as Heterotrophic succession.
Further, based on the nature of environment (primarily moisture conditions) at the start of
the succession, the succession can be of following types:
Hydrarch or Hydrosere: If the succession begins from a water body, it is termed as
Hydrosere or Hydrarch. The water body could be lake, pond, stream, bog or even the
swampy area.
Xerosere or Xerarch: In this case, the succession begins from the dry conditions with very
little moisture content, for example, a desert area, sandy areas, rocks etc. If specifically the
succession starts from the rocky areas, it is known as Lithosere, whereas if it starts from a
sand dune it is known as Psammosere.
Mesosere or Mesarch: If the succession starts in an area with adequate moisture
conditions and temperature, it is known as mesosere or mesarch.
Halosere: Halosere is a type of succession occurring in a saline area i.e. where
concentration of salt in the substratum is very high.
Process of Hydrosere
A hydrosere, also known as hydrarch, starts from a water body like pond, lake or pool that
is gradually converted into a forest through an orderly process. The various plant
communities come in sequence during this succession are grouped into seven main stages
as follows:
Phytoplankton stage: The first organisms that colonize the pond are free-floating blue
green algae or the green algae, diatoms and bacteria. These constitute the pioneers of the
hydrosere. At this time, the substratum is free of any organic matter or soil and the pH of
the water is also very low. However, when such organisms grow for some time and
complete their life cycle some organic matter is added into the substratum and gradually
the environment of pond becomes favourable for other community and unfavourable for
exiting community. Besides organic matter, some silt or the sediments are brought from
the adjoining areas by wind or the wave action of the pond water.
Rooted submerged stage: Rooted submerged hydrophytes (aquatic plants with roots but
remain under water) like Hydrilla, Utricularia, Elodea, Vallisenaria and Potamogeton invade
when the pond is a bit shallower and contains organic matter. These plants grow for some
time and after their death and decay, further build up the substratum and gradually the
water level of the pond decreases and it becomes shallower. With this change in
environment, the conditions become favourable for some other community.
Rooted Floating Stage: Several root bearing plants and having large floating leaves invade
the pond, when it is about 2-5 feet deep. These are Nelumbo, Nymphaea, Trapa and
Monochoria. These become associated with other free-floating plants like Lemna, Salvinia,
Azolla and Wolffia. With the dense growth of these plants, the water level of the pond
further decreases and becomes rich in salts and organic matter. Lot of sediments also
accumulates in the pond at this time and the environment of pond becomes suitable for
some other types of plants.
Reed-Swamp Stage: This stage is dominated by plants Typha, Sagittaria and Scirpus. The
roots of these plants remain buried in the muddy soil while their above ground parts are
exposed to air. This stage is also known as amphibious stage since plants are found in the
semi-aquatic conditions. Due to dense growth of these plants, more and more biomass and
soil is added and the conditions of pond become inhospitable for the present community
and thus new community starts colonizing.
Sedge-Meadow stage: At this time, the pond becomes very shallow with reduced water and
accumulated soil rich in salts and organic matter. The species that colonize such areas are
the grasses and sedges. They also form a dense growth and due to higher rates of
transpiration, the water level of the pond decreases a lot and the conditions become almost
mesic which are ready to support different plants.
Woodland stage: With the pond becoming constantly drier, many terrestrial plants invade
the area and establish there. These are mostly the shrubs and the tree species. Due to the
growth of these plants, the area becomes rich in humus, minerals and a variety of microbes.
The conditions may favour the establishment of tree species.
Forest stage: When the pond is completely turned into land, many tree species invade the
area depending upon the climatic conditions. In tropical areas, the tropical woody species
becomes established, whereas in the temperate areas suitable temperate species colonize.
With the establishment of tree species, several other herbaceous plants get established in
the floor of the forest. The forest becomes self sustainable and is in harmony with the
climatic conditions.
The community matures into a forest and lasts for a longer time. This mature community is
known as Climax community.
This type of succession starts from a rock, which is in un-weathered state and lacks any
organic matter or moisture content. At this stage, only the simple plants like lichens can
colonize. The lichens are then followed by various other plants that contribute towards
building up of the soil substratum congenial for supporting a mature forest community.
Various plant communities that colonize in succession one after the other are summarized
as under:
Crustose-lichen stage: The first organisms colonizing the rock are lichens, which stick to
the surface of rocks and form a crust. These constitute the pioneers of the lithosere. At this
stage, the substratum of rock is hard without any organic matter and poor moisture
content. In such a harsh environment, only the hardy species of lichens like Rhizocarpon or
Lecanora can survive. These lichens release some acidic substances in the substratum
that brings about weathering of rock and besides after the completion of life cycle of these
lichens some organic content is added to the rock substratum that enriches it. Gradually,
the rock substratum changes and a thin layer of soil is added to it that contains some
organic matter also. This becomes unsuitable for the crustose lichens and soon the other
organisms like foliose type of lichens colonize the rock.
Moss stage: With the appearance of a thin soil layer enriched with humus, the rock surface
become suitable for some moss species particularly the xerophytic ones that can survive in
the dry environment. Such moss species are Polytrichum, Tortula or Grimmia. After the
completion of life cycle of these moss species, more biomass and moisture adds to the
substratum and thus the soil layer becomes quite thick and able to support herbaceous
species.
Herb stage: With the change in the habitat of rock (a thick layer of soil with organic matter,
moisture or minerals), many herbs start invading. These include many grasses that grow
there for some time. With their growth, the rock surface is further broken down into
smaller pieces and soil layer becomes thick retaining more moisture, minerals or organic
matter. After completion of their growth, soil becomes more enriched and the conditions of
the substratum no longer remain xeric. Soon the shrubby vegetation with perennial habit
appears there.
Shrub stage: The shrubs appear at this stage when the soil substratum is quite built up
after weathering of the rock. With their excessive growth, these overshadow the grasses
and herbaceous vegetation and further add organic matter into the soil after their
completion of life cycle. At this stage, many tree species invade the substratum that
gradually converts the area into forest.
Forest stage: When the rock completely converts into land, many tree species invade the
area depending upon the climatic conditions. These establish themselves and form
association with several other herbaceous and shrubby plants. The forest so developed
becomes self sustainable and maintains a balance with other biotic and abiotic
components. This forest community stays for a longer time and is known as Climax
community.
COMMUNITY ECOLOGY
1. What are ecological communities?
Definition
A community is a collection of populations of all the organisms which occur together in a
given place and time. Community ecology is the study of the interactions between these
organisms, and the interactions between the organisms and their environment. Communities
can have emergent properties which arise from these interactions - properties which could
not be predicted by studying the individual populations in isolation. Traditionally, the term
‘community’ has had restricted use to describe the activities of the populations only,
whereas when these are combined with the physical environment (e.g. nutrient dynamics
and energetics) the term ecosystem has been used. However it is not possible to consider
the biological ‘community’ in isolation from its environment, therefore the traditional
distinction between ‘community’ and ‘ecosystem’ will not be recognized in these lectures.
The term ‘community’ is also commonly used to refer to a subset of populations within the
whole community, for example we talk about plant communities, insect communities,
arthropod communities, small mammal communities, etc.
Species interactions
Within communities there are a variety of ways in which organisms can interact with each
other. There are also a variety of ways in which these interactions have been classified by
ecologists.
1. Competition (BHT pp. 197-209, 240-247)
Competition occurs when the interaction between organisms results in a reduction of
growth, survival or reproduction for both partners of the interaction.
Exploitation competition commonly involves the use of a limiting resource - some factor
which
is in short supply and is required for growth etc. by each competitor. Limiting resources for
plants include light, water and nutrients, for animals they include food, shelter and nesting
sites. Interference competition occurs when individuals directly interact, such as two
animals fighting for a territory, or allelopathy - the production of chemicals by one
organism which are toxic to another. Competition can be of two types: Intraspecific
competition occurs between
individuals of the same species/population (figure 1), e.g. self thinning in crops or forest
plantations, competition for females among kangaroo males. Interspecific competition
involves individuals from different species/populations (figure 2), e.g. weeds and the crop
in an agricultural field, marsupials and birds competing for nesting sites in dead trees.
2. Predation
Predation is the consumption of one living organism (prey, plant or host) by another
(predator, grazers or parasite). The key idea is that one member (the predator) benefits to
the detriment of the other (the prey). Note that this definition does not include detritivores
- those organisms which consume dead organic matter.
Below are three classes of interaction which come under the category of predation.
‘True’ Predation: This is predation in the ordinary sense where a predator kills and
consumes a prey species. True predators are such organisms as tigers and birds of prey.
Animals which kill and eat other animals are called carnivores. Insectivorous plants can
also be considered true predators.
Parasitism: Parasites are generally much smaller than their host and grow and/or
reproduce inside (endoparasites) or on the surface (ectoparasites) of the living host. They
directly divert some of the resources (water, food) from the host. Many parasites are
animals, e.g. flatworms (Platyhelminthes) and roundworms (Nematodes), but there are
also parasitic plants (e.g. mistletoes, Euphrasia sp.) and some species of fungi.
3. Mutualism (BHT Chapter 13)
Mutualism occurs when both populations/individuals benefit from the presence of each
other. For example many plants have a mutualistic interaction with mycorrhizal fungi
which live on, or in, the root surface. The fungi provide mineral nutrients to the plant, and
in return receive carbon compounds from the plant (Figure 3).
The above categories are based on pairwise interactions, i.e. between a single predator and
a single prey. In ecological communities there are usually many more than two species
interacting at any given time. When more than two species interact, the nature of the
pairwise interactions can be distorted or even reversed (Figure 4). Ecologists are still
trying to understand the complexities and importance of such multi-species interactions.
Do communities exist?
The question of whether communities have properties of their own which are more
than the sum of their parts has been debated for a long time. Much of this debate has
centred around the role that the species interactions play in determining the species
composition of ecological communities. There are two extreme views.
The Clementsian or superorganismic view of communities (Clements 1916) sees
them as being tightly organised entities, where the growth and development of whole
communities is seen to be analogous to the growth and development of an individual.
Under this view, communities exhibit properties which are more than the sum of the
individual parts. Species interactions are assumed to play a major role in the
development and regulation of communities.
An alternative view is the individualistic concept of community structure, originally
attributed to Gleason (1926). Under this view communities are not tightly structured,
but are merely coincidences resulting from chance dispersal, environmental sorting
and species interactions. Thus, communities are less predictable, and species
interactions have a much reduced role in determining the structure of communities.
Guilds: A guild is a group of species which utilise resources in a similar way (Root 1967).
For example a group of fruit eating birds in a rainforest, a guild of forest-floor dwelling
herbs. Note that because species within a guild utilize the same resources, then we expect
them to compete more strongly with each other than with species from different guilds.
Functional types: Functional types are groupings of organisms which respond similarly to
a particular disturbance (Gitay and Noble 1997). The groupings can include species, or
subspecies, or phenotypes which differentially respond to the disturbance, or even
different stages in the life history of the same species. We will be returning to the concept
of functional types later on.
Trophic levels: Community structure can be described by the use of food webs. A food web
is a graph of the various trophic levels in a community (carnivores, herbivores, producers)
and the links between them.
Figure 6 is an example of an actual food web.
2. Mechanisms structuring ecological communities
The ecological niche: definition and measurement (BHT PP. 75-78)
The ecological niche of a species is a multidimensional description of its resource needs,
habitat requirements and environmental tolerances (Hutchinson 1957). The fundamental
niche is the potential set of conditions which a species can occupy. It can be determined
experimentally. However, in nature due to the effects of competition, enemies and
biogeography, species do not occupy the niche entirely.
What is observed is their realized niche (Figure 7).
The niche concept can be further split into two distinct aspects.
Geographic niche, Conditions niche or Beta niche: This simply states that some species
live in different places due to differences in environmental tolerances. Therefore, species
with differing beta-niches never physically come together to interact.
Resource-specialization niche or Alpha niche: Here several species can co-occur in the
same place, i.e. they have the same beta niche. For two species to have different alpha
niches implies they are using different resources, or are using similar resources in such a
way that overlap in their use is minimized.
Figure 8 shows how desert plants can differ in their alpha-niches - plant A is able to capture
water (the resource) most efficiently from the top layer of soil, whilst Plant B obtains most
of its water from deeper underground.
The Principle of competitive exclusion, also known as Gauss’s principle, states that no
two species which share the same (alpha) niche can permanently coexist - the superior
competitor will eventually exclude the weaker competitor. Coexistence between
competitors is therefore related to the amount of overlap between species with similar
niches (Figure 9). For example, in Figure 8 plants A and B might be expected to coexist
because they utilize water from different depths, and hence competition for water is
reduced.
Competition between species with similar niches can lead to shifts in the niche space of a
species through the action of evolution via natural selection (see Evolutionary Concepts
lecture notes). When such a shift is associated with morphological changes it is referred to
as character displacement (Figure 10).
An example of the practical use of the ecological concepts of the niche and competitive
exclusion is in ‘mixed’ or ‘intercropped’ agricultural systems. In such systems two or more
crops are planted simultaneously. If the harvest of this mixture is somehow ‘better’ than if
any of the component species were planted only by themselves (monoculture), then this is
called intercrop advantage. Common intercropping combinations include sorghum &
pigeonpea, corn & bean and corn and wheat. Biologically, intercrop advantage can result
from two possible mechanisms. Firstly, the various crop species in the mixture can be
chosen so that they do not compete strongly with each other, i.e. their niche overlap is
sufficiently low. Secondly, an increase in crop performance can arise if the species are
chosen so that one species modifies the environment in a positive way for a second species,
for example one crop providing shelter for another that otherwise would not perform well
at full sunlight. Note that the ‘biological’ reasons for intercropping, i.e. increasing
productivity/yield may not be the most important in many situations. For example
inter-cropping may result in more efficient use of resources such as land, water, time
etc. and there may be socio-economic advantages such as improved human
nutrition. The book by Vandermeer (1989) provides an excellent introduction to the
topic.
3. Methods used to describe ecological communities
Indices: Indices summarize the data into a single number (the index) by combining, and
hence simplifying, the information. For example, the number of species in the community
(species richness) is a very simple index. We’ll see a number of such diversity indices below
under section 4.
Multi-variant methods: These are statistical tools which allow us to identify species
groupings according to their patterns of co-occurrence. An Ordination is a map which
groups sampling units together on the basis of their similarity of species composition and
abundance (Figure 13). The axes of the ordination are derived mathematically from the
raw data, and they can be thought of as summaries of the community patterns. The scatter
of the points in the ordination can then be used to see if the derived gradients correspond
to gradients in environmental variables. Numerical classification is another method
commonly employed by ecologists to summarize community patterns. With classification
the sampling units are grouped together in sets and sub-sets corresponding to similarity in
species composition. Performing a classification effectively imposes discrete boundaries to
the communities (Figure 14). The literature on the use of multivariate methods in ecology
is very large.....and often very confusing.
Richness, abundance and dominance
A community can be described by list of all the component species and their abundances.
Although species are the most common ‘currency’, higher level groupings of species such as
guilds (section 1.4) can also be used. The total number of species is the species richness.
Abundances can be quantified in terms of the number of individuals, biomass or cover.
Abundances can be expressed either absolutely (e.g. how many individuals per species) or
relatively (e.g. what proportion of the total for each species). Species can be ranked
according to their abundances; the most abundant ones are said to be dominant, and the
ranking is called a dominance ranking. The concept of diversity is considered in greater
detail below.
4. What is (bio)diversity?
Definition
“Biological Diversity is the variety of all life forms: the different plants, animals and
microorganisms, the genes they contain and the ecosystems they form”2. Note the
breadth of this definition; it covers not only diversity in terms of the number of species, but
also the genetic information contained within individual organisms, as well as the diversity
of habitats, natural communities and ecological processes in the biosphere.
The different levels of diversity
Most commonly, the term diversity refers to species diversity which is a measure of
how many species are present in a community and their relative abundances. Although the
species is the most commonly used taxonomic level, studies at bio-geographical scales also
quantify diversity of genera (generic diversity) or families to compare regions. Genetic
diversity is a similar measure which quantifies the variety of genotypes within a species or
population. Humans have long been aware of the concept of genetic diversity through
selection of crop plant varieties and domestic animals. More recently, the concept of
landscape diversity has been developed to refer to the diversity of communities (or
vegetation types) present at the scale of the landscape.
A. Genetic diversity (BHT PP. 34-39)
Definition
Strictly speaking, genetic diversity refers to the diversity of genotypes within a population
or species. The term can be used for a given trait (e.g. the colour of corn grains, resistance
to disease). More generally, it is used to describe the total level of diversity for all traits.
Populations which appear to be genetically distinct from other of the same species are
referred to as a subspecies (a geographically recognizable population). Human modified
genotypes are called races (for animals, Figure 15) and varieties (for plants, Figure 16).
Indeed, the concept has been applied in agriculture and animal breeding for a long time,
where breeders have been using the natural genetic diversity of wild ancestors and
relatives of the cultivated varieties to produce new varieties.
Where pi is the proportional abundance of each species. The effect of including abundances
can be seen from an examination of Figure 18. Note that these indices incorporate both
differences in abundance and richness. Sometimes we want to just consider the relative
abundances of the species independent of the species richness, to see how evenly they are
distributed. This can be done by expressing D or H as a percentage of the value that would
be expected if all species were equally abundant.
This is simply done by dividing D by the species richness (s), and dividing H by the
logarithm of s. In particular, note that although communities 1 and 2 have the same
number of species (s = 5), community 1 is much more diverse (D = 5.0 cf. 1.06, H = 1.61 cf.
0.21). Also note that although communities 1 and 3 have different numbers of species, they
have the same degree of evenness (D/s = 1, H/ln(s) = 1).
Measures of diversity at different spatial scales
Different spatial scales are recognized when considering diversity. Alpha-diversity refers
to the diversity within a single stand or community sample. Beta-diversity refers to the
diversity between community samples.
Explaining beta-diversity generally poses few problems; we know that different species are
often found in different environments. In contrast, explaining alpha diversity can be
extremely difficult. One of the most famous discussions of alpha diversity is Hutchinsons
(1961) 'paradox of the plankton', where he questioned how so many species of
phytoplankton can coexist given that they all live in the same environment and they all
compete for the same basic resources (e.g light & nutrients).
Gamma-diversity refers to diversity at the regional scale - i.e. the combination of alpha-
and beta- diversity. Species diversity also varies temporally, as we will see in a later lecture
(Environmental variability, succession and invasion).
Figure18. Three hypothetical communities illustrating the various measures of species
diversity
Figure 24. Elton’s evidence for his claim that community stability should increase with
complexity (from BHT).
More recently, mathematical analyses have (in general) predicted the opposite trend that
communities with less species tend to be more stable. However, depending on the
assumptions used in these models the opposite prediction can also be generated.
Unfortunately, the evidence from natural communities is both sparse and inconclusive.
Figure 25 shows the results from two recent studies, both of which imply that the species-
rich plant communities studied were more resistant to disturbance than comparable
species-poor communities, suggesting that preservation of biodiversity is essential for the
maintenance of these communities. To conclude, the relationship between complexity and
stability cannot be conveniently generalized, as was originally hoped. It depends on the
type of disturbance applied, and the particular characteristics of the community to which it
is applied.
BIODIVERSITY CONSERVATION
IMPORTANT TERMS
Genetic
Species
Ecological
Genetic Diversity: Genetically uniform populations are highly prone to diseases, harsh
environment.
There are more than 50,000genetically different strains of rice and 1000 varieties of
mango in India.
Species Evenness- the related abundance with which each species is represented in an
area.
The Western Ghat has greater diversity of amphibian species than Eastern Ghat.
Constant environment has promoted niche specialization and greater species diversity.
Species richness increase with increased explored area but only up to a limit.
The relationship for a number of texa is found to be a rectangular hyperbola.
The relationship becomes linear and described by the equation:
LogS=LogC+ZlogA
Where S= species richness, Z is slop of line and A is equal to area, while C is equal to y-
intercept.
Importance of Species Diversity to Ecosystem:
More species tend to be more stable than those with less species A stable community has
following attributes It shall not show too much variation
It must be either resistance to seasonal disturbances and also to invasion by alien species
Loss of biodiversity
IUCN Red list (2004) documents the exactions of 784 species in last 500 years including
359 invertebrates ,338 vertebrates and 87 plants
Extinct animals are:
Steller's sea cow
Dodo
Quagga
Three sub species of tigers
27 species have become extinct in last 20 years alone Loss of biodiversity in a region can
lead to following:
Decrease in plant production
Lowered resistance to environmental perturbation
Increased variability in ecosystem processes like water use, pest cycle, plant productivity
Causes for loss of biodiversity
Habitat loss and fragmentation
Over -exploitation
Invasion of Alien species and
Co-extinction
Conservation of biodiversity
Reasons:
Narrowly utilitarian Broadly utilitarian Ethical
Approaches to Biodiversity conservation
In- situ conservation
eg: biosphere Reserves, national parks, wild life sanctuaries and sacred grooves Ex -situ
conservation
Eg: Botanical garden, zoo, gene bank and tissue culture Conservation of biodiversity
II. The earth Summit; Held in Reo de Janerio in 1992. For conservation of biodiversity
and sustainable utilization of benefits of biodiversity.
III. The world Summit on Sustainable Development; held in 2002 in Johannesburg, South
Africa, to achieve a significant reduction in current rate of biodiversity at global ,
regional and local level by 2010.
ONE MARKS QUESTIONS
1. Microorganisms are part of wild life. Do you agree?
Ans: Yes
2. Which pests attack the high yield varieties of rice a few years ago?
Ans; 1/3
11. Which animals are captured in large numbers for pet trade?
12. What is the major reason for the decrease and extinction of wild life of our country?
Ans: Laxity on the part of the officials in the enforcement of the wild life protection
act.
Ans: 21
Ans: wild life acts as gene bank and provide research materials to produce new varieties /
species.
19. Which useful material is derived from the bask of Cinchona plant?
Ans: Anti malarial drug-quinine
21. Which animal from India become extict due to excess hunting?
Ans: 10%
Ans: Scavengars.