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A prothallium, or prothallus (from Latin pro = forwards and Greek θαλλος (thallos) = twig) is usually the gametophyte stage in the life of a fern or other pteridophyte. Occasionally the term is also used to describe the young gametophyte of a liverwort or peat moss as well.

The prothallium develops from a germinating spore. It is a short-lived and inconspicuous heart-shaped structure typically 2-5 millimeters wide, with a number of rhizoids (root-like hairs) growing underneath, and the sex organs: archegonium (female) and antheridium (male). Appearance varies quite a lot between species. Some are green and conduct photosynthesis while others are colorless and nourish themselves underground as saprotrophs.

Alternation of generations[edit]

Prothallus of the tree fern Dicksonia antarctica (note new moss plants for scale)

Spore-bearing plants, like all plants, go through a life-cycle of alternation of generations. The fully grown sporophyte, what is commonly referred to as the fern, produces genetically unique spores in the sori by meiosis. The haploid spores fall from the sporophyte and germinate by mitosis, given the right conditions, into the gametophyte stage, the prothallus. The prothallus develops independently for several weeks; it grows sex organs that produce ova (archegonia) and flagellated sperm(antheridia). The sperm are able to swim to the ova for fertilization to form a diploid zygote which divides by mitosis to form a multicellular sporophyte. In the early stages of growth, the sporophyte grows out of the prothallus, depending on it for water supply and nutrition, but develops into a new independent fern, which will produce new spores that will grow into new prothallia etc., thus completing the life cycle of the organism.

Theoretical advantages of alternation of generations[edit]

It has been argued that there is an important evolutionary advantages to the alternation of generations plant life-cycle.[1] By forming a multicellular haploid gametophyte rather than limiting the haploid stage to gametes, there is often only one allele for any genetic trait. Thus, alleles are not masked by a dominant counterpart (there is no counterpart).

One benefit of this is that a mutation that causes a lethal, or harmful, trait expression will cause the gametophyte to die; thus, the trait cannot be passed on to future generations, preserving the strength of the gene pool.[1] Furthermore, if individual cells of the gametophyte compete with one another, somatic mutations that reduce cell vigour may prevent a cell lineage from reproducing.[1]


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