Daffodil flowers extend laterally from the long axes of their stems; as a result, wind on a flower exerts torsional as well as flexural stress on the stem. Stems respond by twisting, and thus flowers reorient to face downwind in moderate winds, in the process reducing their drag by ϳ30%. This repositioning is facilitated by the stems' relatively low torsional stiffness. Daffodil stems have a ratio of flexural to torsional stiffness of 13.27 Ϯ 0.96 (SD), compared with 8.33 Ϯ 3.20 (SD) for tulip stems, which bear flowers as symmetrical extensions of their long axes, and compared with 1.5 for isotropic, incompressible, circular cylinders.

Most biological beams bend and twist relatively easily compared to human-made structures. This paper investigates flexibility in 57 diverse biological beams in an effort to identify common patterns in the relationship between flexural stiffness and torsional stiffness. The patterns are investigated by mapping both ideal and biological beams into a mechanospace defined by flexural and torsional stiffness. The distribution of biological beams is not random, but is generally limited to particular regions of the mechanospace. Biological beams that are stiff in bending are stiff in torsion, while those that bend easily also twist easily. Unoccupied regions of the mechanospace represent rare combinations of mechanical properties, without proving that they are impossible. The mechanical properties of biological beams closely resemble theoretical expectations for ideal beams. Both distributions are potentially being driven by the interdependence of the material and structural properties determining stiffness. The mechanospace can be used as a broadly comparative tool to highlight systems that fall outside the general pattern observed in this study. These outlying beams may be of particular interest to both biologists and engineers due to either material or structural innovations.

Foetal dolphins (Tursiops truncatus) are bent ventrolaterally, such that the tailflukes and lower jaw are juxtaposed. The lateral flexibility required en utero may compromise the efficiency of the dorsoventral oscillations required of the swimming neonate. The m. intertransversarius caudae dorsalis (IT) is the most laterally placed epaxial muscle. Bilateral contractions of the IT could limit lateral deformations of the flexible tailstock of the early neonate. We test the hypothesis that the IT is functioning as a postural muscle in neonates by examining its morphological, histological and biochemical properties. The neonatal IT has a relatively large cross-sectional area and bending moment, as well as a large proportion of slow-twitch fibres and elevated myoglobin concentrations. Our results demonstrate that the IT is functionally capable of performing this specific postural function in neonatal dolphins. In later life-history stages, when postural control is no longer needed, the IT serves to fine-tune the position of the tailstock during locomotion. The changing function of the adult IT is concomitant with changes in morphology and biochemistry, and most notably, with an increase in the proportion of fast-twitch fibres. We suggest that these changes reflect strong selective pressure to improve locomotor abilities by limiting lateral deformations during this critical life-history stage.

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Lily pads (Nymphaea odorata) exhibit heterophylly where a single plant may have leaves that are submerged, floating, or above (aerial) the surface of the water. Lily pads are placed in a unique situation because each leaf form is exposed to a distinctly different set of mechanical demands. While surface petioles may be loaded in tension under conditions of wind or waves, aerial petioles are loaded in compression because they must support the weight of the lamina. Using standard techniques, we compared the mechanical and morphological properties of both surface and aerial leaf petioles. Structural stiffness (EI) and the second moment of area (I) were higher in aerial petioles, although we detected no differences in other mechanical values (elastic modulus [E], extension ratio, and breaking strength). Morphologically, aerial petioles had a thicker rind, with increased collenchyma tissue and sclereid cell frequency. Aerial petioles also had a larger cross-sectional area and were more elliptical. Thus, subtle changes in the distribution of materials, rather than differences in their makeup, differentiate petiole forms. We suggest that the growth of aerial petioles may be an adaptive response to shading, allowing aerial leaves to rise above a crowded water surface.