Ecotypes
are organisms which belong to the same species but possess different
phenotypical features as a result of environmental factors such as
elevation, climate and predation. Ecotypes can be seen in wide
geographical distributions and may eventually lead to speciation.
Definition
In evolutionary ecology, an ecotype, sometimes called ecospecies, describes a genetically distinct geographic variety, population, or race within a species, which is genotypically adapted to specific environmental conditions.
Typically, though ecotypes exhibit phenotypic differences (such as in morphology or physiology) stemming from environmental heterogeneity, they are capable of interbreeding with other geographically adjacent ecotypes without loss of fertility or vigor.
Summary
An
ecotype refers to organisms which belong to the same species but have
different phenotypical characteristics as a result of their adaptations
to different habitats. Differences between these two groups is attributed to phenotypic
plasticity and are too few for them to be termed as wholly different
species. Emergence of variants of the same species may occur in the same
geographical region where different habitats provide distinct ecological
niches for these organisms. Examples of these habitats include meadows,
forests, swamps, and sand dunes. Where similar ecological conditions occur in widely separated places,
it is possible for a similar ecotype to occur in the separated
locations. An ecotype is different from a subspecies, which may exist across a number of different habitats. In animals, ecotypes owe their differing characteristics to the effects
of a very local environment which has been hypothesized to lead to
speciation through the emergence of reproductive barriers.Therefore, ecotypes have no taxonomic rank.
Terminology
Ecotypes are closely related to morphs or polymorphisms which is defined as the existence of distinct phenotypes among members of the same species. Another term closely related is genetic polymorphism;
and it is when species of the same population display variation in a
specific DNA sequence, i.e. as a result of having more than one allele
in a gene's locus. In order to be classified as such, morphs must occupy the same habitat at the same time and belong to a panmictic population (whose members can all potentially interbreed). Polymorphism are maintained in populations of species by natural selection. In fact, Begon, Townsend, and Harper assert that
There is not always clear distinction between local ecotypes and genetic polymorphisms.
The notions "form" and "ecotype" may appear to correspond to a static phenomenon, however; this is not always the case. Evolution occurs continuously both in time and space, so that ecotypes
or forms may qualify as distinct species in a few generations. Begon, Townsend, and Harper offer the following analogy:
... the origin of a species, whether allopatric or sympatric,
is a process, not an event. For the formation of a new species, like
the boiling of an egg, there is some freedom to argue about when it is
completed.
Thus ecotypes and morphs can be thought of as precursory steps of potential speciation.
Research indicates that sometimes ecotypes manifest when separated by
great geographical distances as a result of genetic drift that may lead
to significant genetic differences and hence variation. Ecotypes may also emerge from local adaptation of species occupying
small geographical scales (<1km), in such cases divergent selection
due to selective pressure as a result of differences in microhabitats
drive differentiation. Hybridization among populations may increase population gene flow and reduce the effects of natural selection.Hybridization here is defined as when different but adjacent varieties of the same species (or generally of the same taxonomic rank) interbreed, which helps overcome local selection. However other studies reveal that ecotypes may emerge even at very
small scales (of the order of 10 m), within populations, and despite
hybridization.
In ecotypes, it is common for continuous, gradual geographic
variation to impose analogous phenotypic and genetic variation, a
situation which leads to the emergence of clines. A well-known example of a cline is the skin color gradation in
indigenous human populations worldwide, which is related to latitude and
amounts of sunlight. Ecotypes may display two or more distinct and discontinuous phenotypes even within the same population. Ecological systems may have a species abundance that can be either bimodal or multimodal. Emergence of ecotypes may lead to speciation and can occur if conditions in a local environment change dramatically through space or time.
Ecotype and speciation
Just
as sunlight can appear as a dim crack in the sky before clouds part,
the coarse boundaries of ecotypes may appear as a separation of
principle[sic] component clusters before speciation.
— David
B. Lowry, Ecotypes and the controversy over stages in the formation of
new species, Biological Journal of the Linnean Society.
The birth of the term 'ecotype' originally came from early interest in understanding speciation. Darwin argued that species evolved through natural selection from variations within population which he termed as 'varieties'. Later on, through a series of experiments, Turresson studied the effect
of the environment on heritable plant variation and came up with the
term 'ecotype' to denote differences between groups occupying distinct
habitats. This, he argued, was a genotypical response of plants to habitat type
and it denotes a first step toward isolating reproductive barriers that
facilitate the emergence of 'species' via divergence and, ultimately,
genetic isolation. In his 1923 paper, Turesson states that variation among species in a
population is not random, rather, it is driven by environmental
selection pressure. For example, the maturity of Trifolium subterraneum,
a clover which was found to correlate to moisture condition; when sown
in low rainfall areas of Adelaide after a few years the population would
consist of genotypes that produced seeds early in the season (early
genotype), however in higher rainfall areas the clover population would
shift to mid-season genotypes, differences among population of Trifolium subterraneum is in response to the selective action of the habitat. These adaptive differences were hereditary and would emerge in response to specific environmental conditions. Heritable differences is a key feature in ecotypic variation. Ecotypic variation is as a result of particular environmental trends. Individuals, which are able to survive and reproduce successfully pass
on their genes to the next generation and establish a population best
adapted to the local environment. Ecotypic variation is therefore described to have a genetic base, and
are brought about by interactions between an individual's genes and the
environment. An example of ecotype formation that lead to reproductive isolation and
ultimately speciation can be found in the small sea snail periwinkle, Littorina saxatilis. It is distributes across different habitats such as lagoons, salt
marshes and rocky shores the range of distribution is from Portugal to
Novaya Zemlaya and Svalbard and from North Carolina to Greenland. The polymorphic snail species have different heritable features such as
size and shape depending on the habitat they occupy e.g. bare cliffs,
boulders and barnacle belts. Phenotypic evolution in these snails can be strongly attributed to
different ecological factors present in their habitats. For example, in
coastal regions of Sweden, Spain and UK, Littorina saxatilis possess different shell shapes in response to predation by crabs or waves surges. Predation by crabs, also called crab crushing, gives rise to snails
with wary behavior having large and thick shells which can easily
retract and avoid predation. Wave-surfs on the other hand, select for
smaller sized snails with large apertures to increase grip and bold
behavior. All this provide the basis for the emergence of different snail
ecotypes. Snail ecotypes on the basis of morphology and behavior pass
these characteristic on to their offspring.
Tundra reindeer and woodland reindeer are two ecotypes of reindeer.
The first migrate (travelling 5,000 km) annually between the two
environments in large numbers whereas the other (who are much fewer)
remain in the forest for the summer. In North America, the species Rangifer tarandus (locally known as caribou), was subdivided into five subspecies by Banfield in 1961. Caribou are classified by ecotype depending on several behavioural
factors – predominant habitat use (northern, tundra, mountain, forest,
boreal forest, forest-dwelling), spacing (dispersed or aggregated) and
migration (sedentary or migratory). For example, the subspecies Rangifer tarandus caribou is further distinguished by a number of ecotypes, including boreal woodland caribou, mountain woodland caribou, and migratory woodland caribou (such as the migratory George River Caribou Herd in the Ungava region of Quebec).
Arabis fecunda, a herb endemic to some calcareous
soils of Montana, United States, can be divided into two ecotypes. The
one "low elevation" group lives near the ground in an arid, warm
environment and has thus developed a significantly greater tolerance
against drought than the "high elevation" group. The two ecotypes are
separated by a horizontal distance of about 100 km (62 mi).
It is commonly accepted that the Tucuxi
dolphin has two ecotypes – the riverine ecotype found in some South
American rivers and the pelagic ecotype found in the South Atlantic
Ocean. In 2022, the common bottlenose dolphin (Tursiops truncatus), which had been considered to have two ecotypes in the western North Atlantic, was separated into two species by Costa et al. based on morphometric and genetic data, with the near-shore ecotype becoming Tursiops erebennus Cope, 1865, described in the nineteenth century from a specimen collected in the Delaware River.
Artemisia campestris subsp. borealis an ecotype of Artemisia campestrisThe aromatic plant Artemisia campestris
also known as the field sagewort grows in a wide range of habitats
from North America to the Atlantic coast and also in Eurasia. It has different forms arccoding to the environment where it grows. One
variety which grows on shifting dunes at Falstrebo on the coast of
Sweden has broad leaves, and white hairs while exhibiting upright
growth. Another variety that grows in Oland in calcareous rocks displays
horizontally expanded branches with no upright growth. These two
extreme types are considered different varieties. Other examples include Artemisia campestris var. borealis which occupies the west of the Cascades crest in the Olympic Mountains in Washington while Artemisia campestris var. wormskioldii grows on the east side. The Northern wormwood, var. borealis has spike like-inflorescences with leaves concentrated on the plant base and divided into long narrow lobes. Wormskiold's northern wormwood, Artemisia campestris var. wormskioldii is generally shorter and hairy with large leaves surrounding the flowers.
The Scots pine (Pinus sylvestris) has 20 different ecotypes in an area from Scotland to Siberia, all capable of interbreeding.
Ecotype distinctions can be subtle and do not always require large
distances; it has been observed that two populations of the same Helix
snail species separated by only a few hundred kilometers prefer not to
cross-mate, i.e., they reject one another as mates. This event probably
occurs during the process of courtship, which may last for hours.
