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Flowers in Columnea appear in the axils of the leaves and generally
occur singly, but can occur in clusters of up to 10 flowers per leaf axil.
In most species only a single, or perhaps two, flowers will be fully open at
each node at any one time.
All
Columnea flowers have the four whorls associated with flowering
plants. These are the calyx, made of sepals, the corolla, made of petals,
the androecium, made of stamens that produce pollen, and the gynoecium,
where the pollen lands and grows downward through the style to fertilize the
egg in the ovary. As in all Geseriaceae, in Columnea the five sepals are fused to each
other, at least to some degree, but often are free from each other at the
tips. The same is true for the five petals. There are four fertile stamens
in each
flower and these are often coherent in pairs of two stamens each.
Coherent indicates that the stamens stick to each other, usually at the tips
of the anthers where the pollen is produced. The bases of the stamens are
fused to the corolla, as they are in all Gesneriaceae, and if you pull the
corolla off the flower, the stamens will come with it. After the pollen is
shed, the filaments will coil up and pull the anthers into the corolla
tube. The gynoecium consists of two fused carpels which for those that are
not botanists will look like a single structure with an ovary, style and
stigma where the pollen lands.
One
of the oddities of Columnea flowers are the corolla appendages that
appear between the corolla lobes of many species of section Trichantha
such as C. minor. These appendages have been used to readily
recognize species in this section and can be small to larger than the
corolla lobes themselves. It is presumed that these have a role in
pollination, but to date we have no solid or clear explanation for these
structures.
Despite the technical fruit character that separates Columnea from
its closest relatives, most species can still be recognized by a combination
of vegetative and floral characters. The epiphytic nature of Columnea
in its natural habitat is certainly not exclusive to this genus, but is most
often shared with species of Drymonia that typically have a
bilaterally symmetrical calyx, whereas species of Columnea always
have a radially symmetrical calyx. The corolla of Columnea is
always tubular although this can vary widely and be strongly pouched like
some species of Nematanthus, have a very narrow limb (the part of the
corolla that is not the tube) that is relatively inconspicuous, or a limb
that is large and flaring.
The
corolla tube also varies widely in its size, in both diameter and length.
The smallest of these is in Columnea minutiflora and C. parviflora
both of which have a corolla
that is often less than a cm in length and only a few mm in diameter, and is
white. In contrast the large, bright red corollas of Columnea
nicaraguensis with its large flaring limb do indeed seem to belong to a
different genus. Corolla colors are typically yellow or red, but can be
orange, violet, white and combinations of these. Many species often have a
bright red corolla tube and a limb that is a contrasting pale green.
The
corollas of Columnea species are considered to be bilaterally
symmetrical, meaning there is one line that will divide the corolla into two
parts, rather than being radially symmetrical where there are numerous
different ways of dividing the corolla into two equal parts (humans are
bilaterally symmetrical whereas car tires are radially symmetrical).
Sometimes this is obvious when we have flowers that have a galea or hood
comprised of the fusion of the two center petals, these are often flanked
by two other petals and the fifth petal is at the "bottom" of the flower,
often curved down or even backward. An example of this is C. gloriosa. However,
even when the corolla lobes are small and inconspicuous, the corolla still
has a bilateral symmetry based on the orientation of the corolla lobes, such
as C. ambigua.
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