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Morphological resemblance between fossils and recent analogs suggests that cyanobacteria are indeed a very old group of bacteria (see Golubic and Seong-Joo 1999) and that at least some morphological traits have been maintained over time (Golubic and Hofmann 1976; Golubic and Campbell 1979; Schopf 1992b).
Morphological traits have been demonstrated to show strong signature of positive selection [15].
Attempts to shed light on this subject using morphological traits have led to hypotheses lacking satisfactory statistical support; it seemed therefore that a different approach was needed.
Loci influencing polymorphic ER of morphological traits have been genetically mapped in Saccharomyces cerevisiae [15], Arabidopsis [12], [16], and Drosophila [17].
Again, this pattern is consistent with our interpretation that morphological traits have largely additive differences.
In three-spined sticklebacks, QTL for similar or identical morphological traits have been identified in some earlier crosses.
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Natural selection of certain prey traits (e.g. morphological traits) has repeatedly been shown to be driven by predation [10] [20].
Variation in morphological traits has been reported within this range.
Stasis of morphological traits has presumably occurred among populations of Tertiary relicts given their high degree of morphological similarity (Wen 1999).
However, interplay between and within heritable and environmental components directing micro- and macroevolution of morphological traits has been questioned (Stearns, 2000).
Our results also provide information about the effect human selection on morphological traits had on shaping the genetic diversity of cultivated grapevine.
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