The structural and developmental diversity of the Podostemaceae is rem
arkable. A comparison of 19 genera (of 48 genera), and 27 species (of
270 species) is presented, covering both subfamilies, the Podostemoide
ae (= Pod.) and Tristichoideae (= Trist.). Assuming the Podostemaceae
to be derived from a typical cormophytic plant with the classical root
-shoot (CRS) model, then evolutionary dynamics of vegetative structure
s in this family include: formation of green crustaceous structures as
a result of dorsiventral flattening of roots, stems or both, reductio
n and loss of root caps, occurrence of sticking rhizoids and often dis
k-like holdfasts, and heterotopy of organ formation (from exogenous to
endogenous bud formation). Some examples of structural dynamics are u
nique to certain taxa, e.g. 90 degrees switch of the dorsiventrality p
lane in leaves of Marathrum, Mourera, and Oserya (Pod.); positional co
rrelation of dithecous leaves (i.e. leaves with two sheaths) and dicho
tomous shoot branching in Podostemum and genera mentioned above (Pod.)
; occurrence of unique leaf-shoot mosaics (called ramuli) in Tristicha
and allies (Trist.). Thus, the structural categories of typical flowe
ring plants are transcended in the Podostemaceae due to developmental
changes and saltational evolution. An overview of reproductive traits
in Podostemaceae is given, focussing on characters that are useful in
traditional systematics: shape, texture, and dehiscence of spathella (
Pod.); presence and shape of cupule (Trist.). Starting with neotropica
l taxa showing radial flower symmetry (e.g. Rhyncholacis, Marathrum pr
o parte), most Podostemoideae can be derived by reduction of the numbe
r of stamens and basal fusion of the two remaining stamens. Most podos
temads are wind-pollinated or autogamous. A few neotropical genera suc
h as Mourera (Pod.) and Weddellina (Trist.) show polyandry, probably a
s an adaptation to insect-pollination. Other taxonomically used charac
ters such as pollen (dyads in many Pod.), ovules, seeds, and capsules
(ribs, dehiscence) are also demonstrated and discussed. (C) 1997 Elsev
ier Science B.V.