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This divergence was attributed to differences among models in the sizes of detrital and humus C stocks in different soil layers to which a uniform set of soil C transformation coefficients was applied during disturbances.
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The extent by which mate choice divergence is attributed to evolution of sex-linked genes should therefore increase with time since divergence between populations.
However, based on the direction of the plastic shift in morphological space of both populations (Fig. 6), it is unlikely that the morphological divergence found in reservoirs was attributed to predator-induced phenotypic plasticity.
Specifically, body shape divergence in reservoir habitats was attributed to posterior movement of the tip of the snout, dorsal movement of the corner of the mouth, posterior movement of the anal fin, ventral movement of the pelvic fin, and anterior movement of the pectoral fin (Table 3).
This locking was attributed to divergence of the transverse axes of the talonavicular joint and the calcaneocuboid joint in the case of calcaneal inversion or plantar flexion.
In addition, a high h and high π indicated high levels of divergence within three regions, which was attributed to secondary contact between previously differentiated allopatric lineages.
The rapid evolution of intron sequence was attributed to sequence divergence ratios in LSC and SSC (Additional file 7: Figure S2).
The proposed divergence from the trend observed with heparin oligosaccharides was attributed to the alternating domain structure of the HS chain.
This improvement was attributed to the lower sequence divergence of RASs, which also expanded the sequence space covered by the microarray.
Later its variability was attributed to vegetation.
The book was attributed to "St.
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