Temporal range: Mid Neogene – Recent 14–0 Ma
Relationships and Evolution
By contrast to other members of Pandanales the family demonstrates stricter flower morphology. Despite that, the flower structure is still quite variable and with a lot of specifics. Thus morphological analyses are not able to uncover realistic phylogenetical relationships neither appropriate taxonomy. Embryological development places the family among the amaryllids while the composition of the ovary puts it near the distinct Hypoxidaceae. However, a study regarding the pollen structure in two genera from Velloziaceae was found to be an important character and suggests some correlation but this is still a variable trait.
Molecular analyses recognize five distinct genera (by including Talbotia in Xerophyta and Nanuza in Vellozia thus forming two sister groups) and show that the monotypic genus Acanthochlamys is sister to the rest of the members. The family originated in Gondwana. The crown group is dated to be very young - 14 Mya (Mid Neogene) but the stem group was found to be much older - 108 Mya (Mid Cretaceous). Velloziaceae has a total of 306 known species.
Distribution and Ecology
Members of Velloziaceae are distributed both in the Old and the New world. Genera as Vellozia, Nanuza and Barbacenia are found in South America (Brazil, Cerrado). Xerophyta and Talbotia are growing across Africa. Plants from the family are also found in Madagascar and the southern part of the Arabian peninsula. One distinct species (Acanthochlamys bracteata) is restricted to China as the only member found in Asia.
Velloziaceae includes different xerophytes inhabiting open and dry habitats. These plants exhibit various adaptations against desiccation as for example less-densely distributed stomata, decreased surface area by the use of developed furrows (as in many cacti) and expansive leaf sheets that cover the stem or the aerial roots until they grow long enough to reach the ground level. In some members these sheets are able to create a microclimate that sustains the roots by keeping a constant level of moisture.
In the majority of Velloziaceae flowers are single or sometimes collected in bracts. There is no definite flowering period. They are hypanthium-forming, sometimes papillate at their base or smooth, mostly white, creme or colored in different shades of purple although species with yellow, orange or red flowers also exist.Despite stricter, their structure is quite variable in some aspects (the number and structure of stamens varies at very high rate) as in other members of Pandanales. Tepals are six. The ovary is divided into three chambers with many ovules developed in them. Pistil and Stigma are also divided into three parts.
Pollen and Pollination
Examination with scanning electron microscope uncovers that one of the distinctive characteristics of the family is the structure of the pollen. Its shape and composition are distinctive. For example, in Barbacenia pollen grains are singular and represent simple monads with ellipsoidal shape and one aperture. In Vellozia the grains are tetragonal (organized in tetrads) and non-apperturate. The size of pollen in Barbacenia is around half the size of that of Vellozia. However, the structure of the exine (pollen's envelopment) is a trait shared by the members of Velloziaceae. It is composed of many reticulations which in many cases may be described as vermiform. In some species, such as Vellozia abietina, the pollen wall does not fit this description, lacking any surface reticulations.
Both cross and self pollination are observed inside the family, and the process is accomplished in various manners. Pollinators of Vellozia include the common honeybee (Apis melifera) and different species of solitary bees as Megachile curvipes, Psaenythia sp. and Augochlora metallica. The reward is pollen which is much more abundant than nectar. Nectar in the genus contains very low concentration of sugars. Bees use the three lobed stigma as a landing platform, and visually orient towards it. When the tepals are removed, bees will visit the flowers, but when the stigma is removed, no pollinators are recorded. It was found that hummingbirds visit these plants despite the diluted composition of nectar. Barbacenia differs in that its nectar is more abundant than its pollen. The pollen is probably taken by carpenter ants but whether ants are successful pollinators is not known. Pollen grains in Barbacenia are smaller, and these insects may be able to carry them and leave some on the stigma while they are searching for nectar. However, hummingbirds were observed on this genus too.
Another characteristic of this family is the longevity of the flowers. Most angiosperms exhibit a relatively definite age of their floral structures, which would subsequently die. There are few exceptions, and among them is the family of Orchids (with Vanda as a remarkable example) while another one is Velloziaceae family. They are able to remain fresh for days until pollination occurs by triggering shriveling. It is supposed that this is due to auxin or ethylene formation.
Fruits and Seeds
Fruits and seeds of these plants appear in large variety of shapes and sizes by demonstrating many different adaptations enhansing dispersal. Such adaptations include the development of bristles or hooks (Talbotia elegans) that cover the seed capsule. This allows attachment to animals by making the seeds able to travel on long distances. Another important characteristic is that the capsule is sticky which also helps to attach. A trait of particular interest regarding the seed structure is the appearance of additional layer formed from the endospermal integument.
- Angiosperm Phylogeny Group (2009). "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III" (PDF). Botanical Journal of the Linnean Society. 161 (2): 105–121. doi:10.1111/j.1095-8339.2009.00996.x. Retrieved 2013-07-06.
- Christenhusz, M. J. M. & Byng, J. W. (2016). "The number of known plants species in the world and its annual increase". Phytotaxa. Magnolia Press. 261 (3): 201–217. doi:10.11646/phytotaxa.261.3.1.
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