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Reversion from xylem vessels to tracheids
In three plant taxa that evolved in environments with frequent freeze-thaw cycles (Winteraceae, Trochodendraceae and cold desert Ephedra), vessel evolution has been reversed independently in favour of a return to a tracheid-based vascular system.
Xylem vessels in vascular plants
Vessels are characteristic of the angiosperms, and yet they have evolved independently in several other groups, including the lycophyte Selaginella, horse-tail Equisetum and the enigmatic Gnetales.
Torus-margo pits in vascular plant xylem
Torus-margo pits probably evolved once in the gymnosperms, after the split of more advanced gymnosperms from the cycads. Surprisingly, eight genera from five families of angiosperms, which are characterised by highly effective xylem vessels, have also evolved torus-margo structures.
Desert plants with succulent stems
Fleshy, succulent stems have evolved in several distantly related desert plant families, including cacti, certain species of Euphorbia and two genera of the family Asclepiadaceae, Hoodia and Stapelia.
Succulent desert plants
Classic examples of convergence in desert plants include the so-called 'stem succulent' cacti in the Americas and cactus-like Euphorbia species in Africa and South Asia, and also the striking similarity between 'leaf succulent' Agave and Yucca of the Americas and Aloe and its close relatives in Africa.
Swimming and thermoregulation in sharks and tuna
Thunniform swimming depends on a large, lunate tail that is joined to the rest of the body via a narrow peduncle. Whilst the tail flicks backwards and forwards, so propelling the animal, the rest of the body hardly moves sideways.
Penis form in mammals, turtles, birds and octopus
The specific case of a penis with a hydrostatic structure, as well as an array of collagen fibres that allows both expansion and guards against aneurysms, has evolved in a strikingly convergent fashion in mammals and turtles.