Ecotype

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ecotype

[′ek·ə‚tīp]

(ecology)

A subunit, race, or variety of a plant ecospecies that is restricted to one habitat; equivalent to a taxonomic subspecies.

Ecotype

a group of similar populations within one and the same plant species that are adapted to certain climatic, edaphic, or cenotic conditions and that have developed, under these conditions, hereditary morphological, physiological, biochemical, and other features. Thus, an ecotype is isolated with respect to distribution; genotypically it is an intraspecific subdivision, which distinguishes it from a biotype.

The term “ecotype” was introduced in the 1920’s by the Swedish scientist G. Turesson. Different plants have different numbers of ecotypes. The ecotypic composition of a species becomes more varied as its geographic range and ecological amplitude increase. For example, 36 ecotypes have been distinguished in the pine Pinus silvestris and 27 in the spruce Picea abies. Ecotypic polymorphism is most clearly manifested at the center of speciation and morphogenesis. In the medic Medicago falcata, for example, there are many ecotypes in the Caucasus and only a few in the northern USSR. Parallel ecotypic differentiation is observed in many species. Thus, the wormwood Artemisia campestris, sheep sorrel (Rumex acetosella), and Silene uniflora, which grow in bright, dry habitats where there are strong winds, develop eco-types with procumbent stems.

Three main groups of ecotypes are distinguished: climatic, edaphic, and biotypic. Climatic, or geographic, ecotypes occupy a separate part of the area of distribution of a species and originated under the influence of specific climatic conditions; for example, in the awnless brome (Bromus inermis), the southern eco-type differs from the northern one by its nanism, narrow rough leaves, and wax coating. Edaphic ecotypes develop under the influence of soil and ground conditions, such as the pine ecotype on the chalky outcrops of the Don River, which has even been described as the independent species Pinus cretácea. Biotypic, or cenotic, ecotypes appear and develop mainly under the influence of plants together with which the given species form plant communities, for example, the field and forest ecotypes of the cocksfoot (Dactylis glomerata) and the forest and dune ecotypes of the narrow-leaved hawkweed (Hieracium umbellatum).

The development of an ecotype is a lengthy process. If an ecotype has progressive characteristics, which permit it to extend the range of the species, it may give rise to a new species, and consequently an ecotype is one of the stages in the process of specia-tion.

REFERENCES

Sinskaia, E. N. Dinamika vida. Moscow-Leningrad, 1948.
Zavadskii, K. M. Uchenie o vide. Leningrad, 1961.
Korchagin, A. A. “Vnutrividovoi (populiatsionnyi) sostav rastitel’nykh soobshchestv i metody ego izucheniia.” In the book Polevaia geobotanika, vol. 3. Moscow-Leningrad, 1964.

KH. KH. TRASS

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An evaluation of variability in the expression of forage characteristics of interest and of the genetic diversity of ecotypes and hybrids of different species of the genus Paspalum by means of a meta-analysis enables the comparison of data from different trials, thus increasing the number of ecotypes, hybrids, and repetitions evaluated.

Forage characters of different Paspalum species in Rio Grande do Sul: a meta-analysis/Caracteres forrageiros de diferentes especies do genero Paspalum no Rio Grande do Sul: uma meta-analise

On the other hand, ecotype G05--known as 'Costena' or 'Ciruela china'--had the maximum values of mass and length (36 g, 45 mm) (Table 2).

Chemical and phenotypic diversity of Mexican plums (Spondias purpurea l.) from the states of Guerrero and Morelos, Mexico/Diversidade quimica e fenotipica das ameixas Mexicanas (Spondias purpurea l.) dos estados de Guerrero e Morelos, Mexico

According to Table 2, for all evaluated traits, considerable variation among ecotypes was observed.

Molecular markers associated with the agronomic traits in the medicinal plant lemon balm/Marcadores moleculares associados aos tragos agronomicos na planta medicinal erva cidreira

In Algeria, a detailed study of hatching processes in controlled conditions, simulating seasonal temperatures changes, showed that the activities of one Algerian ecotype of H.

Effect of Soil Temperature on Juvenile Emergence of Algerian Populations of Heterodera Avenae

Species composition and quantity of the pooled samples of different mowing regimes (LF: life form; EF: ecotype form; M: mowing once a year in May; MS: mowing twice a year in May and September; S: mowing once a year in September; C: abandoned without management; arbu: arbusticol; gra: graminicol; pra: pratinicol; sil: silvicol; hyg: hygrophilic; mes: mesophilic; m-hyg: moderately-hygrophilic; m-ther: moderately-thermophilic; ther: thermophilic).

Effects of different mowing regimes on orthopterans of Central-European mesic hay meadows

Highest value of Magnesium was observed in ecotype E18 which is 102.

ELEMENT CONTENT ANALYSIS OF FICUS PALMATA FORRSK. GROWN IN AZAD JAMMU AND KASHMIR

We recommend reducing block size from 250 x 250 m to 200 * 200 m in the future for two reasons: (1) to avoid inaccuracies in ecotype assignment and (2) to space line transects within the block closer together.

Nesting activity of Kittlitz's Murrelet in the Kakagrak Hills, Northwestern Alaska

In plants subjected to 100% FC, the TLA was higher in seedlings from Laranjeira and lower in the seedlings of BRS-Para; under 130% FC, the TLA was higher in seedlings from Laranjeira and the ecotype Hideo (Table 1).

Morphological and physiological responses of acai seedlings subjected to different watering regimes/Respostas morfologicas e fisiologicas de mudas de acaizeiros submetidas a diferentes regimes hidricos

Honey bee biodiversity in Western Black Sea and evidence for a new honey bee ecotype in Yigilca province.

Determination of Annual Colony Development of the Yigilca Local Honeybee in Turkey and Comparison with Apis mellifera caucasica and A.m. anatoliaca Hybrids

The differentiation of California coastal ecotype bottlenose dolphins from the offshore ecotype has successfully relied on the multiple data types and sources, including analyses of morphology, microbiology and genetics, as well as photo-identification (Walker 1981; Perrin et al.

Possible stock structure of coastal bottlenose dolphins off Baja California and California revealed by photo-identification research

In one of the earliest transcriptome studies of ecotype divergence between marine populations, Barreto et al.

Models of selection, isolation, and gene flow in speciation

Meanwhile, a western mountain ecotype became the source of upland ecotypes that migrated to the arid and semiarid Great Plains, which then became a secondary--not the primary--center of switchgrass diversity.