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5.3 Class Magnoliopsida – flowering plants - Cambridge University ...

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Basal Eudicots<br />

Basal eudicots such as the Proteales and Ranunculales have a pattern<br />

of leaf venation in which the lateral veins terminate at the margin in<br />

a small tooth (craspedodromus). They have a well-developed perianth<br />

but this is poorly differentiated into a calyx and corolla, and has a<br />

variable number of tepals spirally arranged or in whorls of three. Stamens<br />

and carpels are numerous and varying in number. The carpels<br />

are free to connate and have a sessile stigma.<br />

ranunculales (buttercups, poppies and barberries)<br />

Evolutionary trends in the Ranunculales include changes in the symmetry<br />

and the increasing complexity of the flower. Floral parts,<br />

especially the numerous stamens and carpels are commonly spirally<br />

arranged and the fruit is usually a follicle or an achene. The<br />

flower is apocarpous with superior pistils. The poppies, Papaveraceae<br />

(∼660 species) are derived from the buttercups from which they<br />

differ by having a syncarpous gynoecium and only two to three<br />

sepals. There are two subfamilies, the actinomorphic Papaveroideae,<br />

which produce latex, and the strongly zygomorphic Fumarioideae,<br />

which have a clear sap. Another large family in the order, the<br />

Berberidaceae (∼570 species) is distinguished from the Ranunculaceae<br />

by having stamens opposite the petals and a single pistil<br />

which becomes a berry. They have their flower parts in whorls rather<br />

than a spiral with two whorls of stamens and one to two whorls of<br />

nectaries.<br />

proteales (proteas, banksia and grevilleas)<br />

The Proteales are well represented in the Southern Hemisphere. The<br />

family Proteaceae in particular shows a distribution which records<br />

the old Gondwanan supercontinent. The Proteaceae are one important<br />

family (Figure 5.82) where brush blossoms have evolved. Some<br />

relationships discovered by the analysis of DNA sequence data are<br />

distinctly odd. For example, in the Proteales, Nelumbo, the sacred<br />

lotus, and Platanus, the plane tree, are sister groups. If this sister<br />

relationship is true it provides an astonishing reminder of how little<br />

we know about the evolutionary history that connects living plant<br />

groups. What kind of shared ancestor did these two lineages have<br />

and what were the circumstances that led to one becoming aquatic<br />

and the other a tree? The existence of such differences in sister lineages<br />

demonstrate the potential evolutionary fluidity of morphological<br />

characters, and emphasises the fact that living <strong>plants</strong> are only<br />

the tips of a highly branched phylogenetic bush. Within the bush<br />

many branches end blindly and do not reach the surface so that<br />

intermediate linking kinds between living plant groups do not now<br />

exist.<br />

<strong>5.3</strong> CLASS MAGNOLIOPSIDA <strong>–</strong> FLOWERING PLANTS 237<br />

Figure 5.81. Fumarioideae<br />

(Corydalis): (a) plant; (b) detail of a<br />

single flower.<br />

Figure 5.82. Protea: the long<br />

slender flowers are grouped in<br />

heads surrounded by showy<br />

bracts. Each flower has a single<br />

pistil surrounded by four petals<br />

(three fused and one free) with<br />

anthers adnate to the petals.

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