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Morphological analyses were performed by scanning electron microscopy (SEM), and thermal analyses by thermogravimetry (TGA) and differential scanning calorimetry (DSC).
Morphological analyses were performed to determine myotube number, diameter (μm) and myonuclear accretion as indices of differentiation and myotube hypertrophy.
The morphological analyses were carried out through a scanning electron microscopy (model JSM-5600LV, JEOL, Tokyo, Japan) using an applied voltage of 20 kV.
Morphological analyses were conducted at Centro de Microscopia (UFRGS, Brazil) by transmission electron microscopy (TEM; Jeol, JEM 1200 Exll, Japan) operating at 80 kV.
Morphological analyses were performed at each time step for every animal, and a two-way ANOVA with repeated measures was used to analyze the data.
Thermal, mechanical and morphological analyses were performed in order to show the better performances of these blends compared to mechanical ones obtained without the use of the compatibiliser.
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However, until further functional morphological analyses are performed, it is difficult to assess the likely biomechanics of Ar. ramidus.
However, molecular and morphological analyses are not fully congruent since Macrodasyida and Chaetonotida are often resolved as non-monophyletic groups [e.g. 11], [16], [20], [21].
The grouping of Physeteroidea with Ziphiidae, as found in some morphological analyses, was not supported.
Our morphological analyses are concordant with the cross-kingdom host jumps as revealed by molecular phylogenies.
To accurately and thoroughly document this diversity, genetic and/or behavioral investigations, in addition to morphological analyses, are necessary.
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