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Gene-ecological adaptations
(NOTES)
Species differ in their environmental requirements. They also differ in respect
of their tolerance to environmental fluctuations.
The species occur in several morphological forms in different habitat
conditions. Gote Turesson (1922), a Swedish scientist, conducted a series of
experiments on variations within species. He collected a group of 20 or more
individuals of the same species (Plantago maritina) from different areas and
planted them under identical environmental conditions in his experimental
garden at Akark.
Gote Turesson noted that:
Several intergrading forms existed within the species, which differed
from one another in morphological or physiological features.
Some of the differences might be temporary (unstable) and could be
induced only by the environmental factors, while some others might be
permanent (i.e. genetically fixed).
These observations led him to formulate the concept of “gene ecology”, which
brought about many revolutionary changes in plant taxonomy.
The population, sampling and subsequent procedures that Turesson followed
led him to conclude that species differ from one another morphologically,
physiologically and in habitat-requirements. On the basis of such studies, he
proposed the following classes of morphological forms within a species:
1. Ecads 4. Ecospecies and
2. Ecotypes 5. Coenospecies
3. Ecoclines
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1. Ecads
Ecads are also called, ecophenes, epharmones or habitat forms. Ecads may
differ to such an extent that they can be treated as different species. It is
because they carry so diverse environmentally induced variations. Ecads belong
to the same genetic stock and the morphological variations (e.g. in shape, size,
number, reproductive capacity, etc.) between the ecads are induced by the
environmental influences. These variations are not fixed (genetically governed)
but are temporary, somatic and reversible. For example, there are two ecads of
a species, namely Ecad 1 and Ecad 2. If Ecad 1 is transplanted into the
environment of Ecad 2, the differences between the two ecads would
disappear.
The morphological variations of ecads are not permanent because their
genetic composition is same. Since they are identical in their genetic makeup,
they are interfertile forms.
Example 1: Euphorbia hirta plants, growing in the grasslands, are prostrate and
profusely branched (Ecad 1), while the plants of the same species growing on
the footpaths are compact, small and cushioned-leaved (Ecad 2). When these
forms (two ecads) are grown under identical habitat-conditions, their
differences disappear.
Example 2: In Bothriochloa pertusa and Dichanthium caricosum, several
distinct morphological forms of ecads were noted under different habitats by
Pandeya (1962).
In both the above mentioned species there are two ecads:
Basket-shaped habit is shown by the plants growing in protected areas
(no grazing)
Saucer-shaped habit is shown by the plants growing in over-grazed
areas.
Grazing caused morphological variations such as reduction in the size of erect
stem, number of spikes per raceme, number of spikelets per spike and in
length and breadth of lower glumes of spikelets. Grazing also resulted in some
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physiological variations such as development of anthocyanin pigment in the
leaves and early initiation of flowers.
2. Ecotypes
These are also called ecological races or physiological races. The term ecotype
was proposed by Turesson (1922) to the groups of populations or ecological
races or sub-species of a species in relation to different environmental or
habitat-conditions. These are interfertile forms (or biotypes of a species),
which possess different genetic compositions (or genotypes). The ecotypes
arise due to mutations, hybridization and isolation.
Though different ecotypes of a species are morphologically and genetically
distinct, yet because of their interfertility, they are put into one taxonomic
species. Ecotypes are morphologically, physiologically and developmentally
adapted to live under varying environmental conditions. Ecotype is the product
of genetic response of a population to a habitat. In ecotypes, adaptations are
irreversible, i.e. they retain their features even when planted in a neutral
habitat.
The differences in the ecotypes are so marked that some of them have been
treated as separate species by earlier taxonomists.
Example 1: Mishra and Shiva Rao (1948) found Lindenbergia polyantha and
Lindenbergia urticaefolia to be the ecotypes of the same species. The two
ecotypes differ from each other in respect of their tolerance to high doses of
lime (carbonates, oxides and hydroxides of calcium). Lindenbergia polyantha
can tolerate high doses of lime.
Example 2: In another study, Ramakrishnan (1959, 1960) showed that red and
green populations (red ecotype and green ecotype) of Euphorbia thymifolia are
two ecotypes.
The red ecotype is a calcicol (i.e. it grows in calcium-rich soil as well as in
calcium-deficient soils) and the green ecotype is a calcifuge (i.e. it cannot grow
in calcium-rich soil). The red ecotype possesses a pair of dominant alleles,
whereas the green type possesses a pair of recessive alleles.
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Some more examples: ecotypes have been reported in several species of
plants, such as Euphorbia hirta, Cassia tora, Ageratum conyzoides, Cenchrus
ciliaris, etc.
Characteristics features of ecotypes:
1. Ecotypes of a species, though genotypically distinct, are always
interfertile.
2. They retain their original features when cultivated in a natural habitat
3. Variations of ecotypes are genetically fixed
4. Ecotypes occur in distinct habitats
5. Ecotypes are discrete entities with clear differences, which separate one
ecotype from another
6. Differences between ecotypes are not due to plastic response to change
in environment but are actually due to natural selection of locally adapted
populations.
Formation of new ecotypes: Ecotypes are produced by the following methods:
1. Hybridization
The ecotype is produced by the natural cross between two species. For
example, when Spartia stricta is naturally crossed with Spartia altemiflora, the
new hybrid Spartia townsendii results, which eliminates both the parents from
their natural habitats because of its greater adaptability.
2. Mutation
Due to natural mutation (sudden change in genes) and recombination (during
meiosis), small gene pools accumulate in a segregating population, which make
it better-adapted to the particular habitat or environment. Some new ecotypes
also arise by cultivation (or protected growth) as it eliminates competitive
selection.
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