Prothallium
From Wikipedia, the free encyclopedia
A prothallium, or prothallus (from Latin pro = forwards and Greek θαλλος (thallos) = twig) is usually a pteridophyte, i.e. spore-bearing plant, (almost exclusively ferns) in gametophyte stage in the alternation of generations cycle. Occasionally the term is also used to describe the young gametophyte of a liverwort or peat moss as well.
The prothallium of a pteridophyte forms from a spore that has fallen from the sporophyte stage and germinated. 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.
[edit] Alternation of generations
Spore-bearing plants, like all plants, go through a life-cycle of alternation of generations. The fully grown sporophyte, what the layman refers 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 then develops independently for several weeks; it grows sex organs and produces ova and flagellated sperm. After rainfall, the sperm are able to swim to the ova for fertilization to form a diploid sporophyte cell. This cell divides by mitosis and grows out of the gametophyte into a new fern, which will produce new spores that will grow into new prothallia etc., thus completing the life cycle of the organism.
[edit] Advantages of alternation of generations
There are two important evolutionary advantages to the alternation of generations plant life-cycle. Firstly, by forming a haploid gametophyte, there is only one allele for any genetic trait. Thus, all alleles will be expressed because no allele may be masked by a dominant counterpart (there is no counterpart). The benefit of this is that any mutation that causes a lethal, or harmful, trait expression cannot be masked and will cause the gametophyte to die; thus, the trait cannot be passed on to future generations, preserving the strength of the gene pool. Also, crossing-over during meiosis in the formation of spores, and sexual reproduction in the gametophytes, allows for genetic diversity, which also inhibits harmful recessive genes from "surfacing" and being expressed.
