Origin of the Seed
When plants developed the secondary growth, the almost unlimited perspectives opened for enlarging their body. However, these giants faced a new problem.
Big animals like elephants, lions, and whales tend to produce minimal number of offspring but increase the child care to ensure survival. This is called K-strategy(opposite to r-strategy of usually smaller creatures which employs big numbers of offspring, and most of them will not survive).
Analogously, bigger plants would need to do the same as K-strategic animals: make few daughter plants but defend and supply them with all needs until they mature. However, big secondary thickening spore plants were not capable of that; instead, they still made billions of spores and then left them to fend for themselves. Naturally, only few from these billions would survive to become fertilized. Even worse, these spore tree forests were not at all stable: in acciden-tally good conditions, many spores would survive and make sporophytes which start to grow simultaneously and then suppress each other and even die from over-population. But if the environmental conditions are bad, then none of the gametophytes will survive so there would be no new saplings to replace the old trees.
It is similar to the so-called “dinosaur problem”. This situation arose when gi-ant Mesozoic reptiles also lost the control for their offspring: their egg size was limited due to physical restrictions, therefore, young dinosaurs were so much smaller than adults; then the only possible strategy was to leave them alone. As a result, at the end of Mesozoic dinosaurs either decreased in size (became birds), or went extinct. Plants, however, kept their size and survived. This is because they developed the seed (Fig.7.10).
A seed is the result of enforced control of the sporophyte over the gametophyte. The idea of a seed is to hide most of the heterosporous life cycle inside mother plant (Fig.7.11). In seed plants, everything happens directly on the mother sporo-phyte: growing of gametophytes, syngamy, and growing of daughter sporo-phyte. Consequently, the female spore (megaspore) never leaves the sporangium. It germinates inside, waits for fertilization and then the zygote grows into and embryo, still inside the same sporangium.
What will finally leave the mother plant is the whole female sporangium withgametophyte and embryo on it. This is theseed. It can be defined as chimeric structure with three genotypes: seed coat (mother plant megasporangium,2n),endosperm (female gametophyte, n), and daughter sporophyte (embryo, 2n).
It should be noted here that flowering plants have endosperm of different ori-gin; it is called endosperm2 and usually is triploid (3n) whereas female game-tophyte endosperm is haploid (n) endosperm1. The other note is that apart from seed coat (which originates from integument(s), megasporangium ex-tra cover(s)), mother sporophyte also gives nucellus (wall of megasporangium) which sometimes is used as a feeding tissue for the embryo. This last tissue is called perisperm.
One problem is still left. How will sperms reach female gametophyte and egg cell? The target is now high above the ground, on a branch of the giant tree. The only possible solution is pollination. Pollination is the distribution (mostly with wind or insects) of the whole male gametophytes which are called pollengrains. A pollen grain isnot a spore. It contains multiple haploid cells; some ofwhich are sperms.
The lesser problem is: How would these sperms will swim to the egg cell? Some seed plants will excrete the drop of liquid from the top of the ovule (integu-ment(s) + megasporangium), whereas the other, more advanced way is to grow a sperm delivery tool, the pollen tube (Fig. 7.12) made from one of the pollen grain cells. Fertilization with pollen tube is often called siphonogamy.
Consequently, seed plants with the pollen tube do not have flagella even on male gametes; these cells are spermatia. (Below, we will continue to call all male gametes “sperms”). Pollen tube also allows only two male gametes per game-tophyte: in living world, male gametes are usually competing for fertilization— this selects the best genotypes; whereas in higher seed plants, competition is between pollen tubes. Haploid pollen tube grows inside alien tissue of diploid sporophyte, so this growth is extremely slow in many seed plants. However, an-giosperms made their pollen tubes to grow fast.
The cycle of a seed plant (Fig. 7.13) begins with a sporophyte (2n) and has both the female and male organs where some cells undergo meiosis. Inside the ovule (which is the megasporangium with extra covers), female gametophyte (n, fu-ture endosperm1) produces the egg cells. Male gametophytes (pollen grains) ripen in the pollen sacwhich is the microsporangium. The pollen sac sends out the pollen grains which meet up with the ovule. The pollen grain then re-leases the sperms which fertilize the egg cell, and a zygote is formed. The zygote grows into embryo (which uses endosperm as a feeding tissue) and then into the sporophyte.
Seeds are diverse. For example, in an onion (Allium), a seed (Fig. 7.14) has en-dosperm, one cotyledon (embryonic leaf), radicle (embryonic root), and the lat-eral embryonic bud (plumula).
Beans (Phaseolus) and other Leguminosae are examples of seeds without endo-sperm—actually, it was there, but growing embryo usually eats it out completely. These seeds have two large cotyledons. Grass (Gramineae) seeds contain several specific organs, namely coleoptile, coleorhiza, and scutellum. The scutellum is an enlarged cotyledon, coleoptile is the bud cover, and coleorhiza covers the em-bryonic root, radicle (Fig. 7.15). Onion and grasses are monocots with lateral embryonic bud. Other seed plants have a terminal embryonic bud and two or multiple cotyledons. Pine (Pinus) is an example of a plant that has multiple (five or more) cotyledons. Some plants like orchids (Orchidaceae) do not have de-veloped embryo and even endosperm in seeds, their germination depends on a presence of symbiotic (mycorrhizal) fungus.
The first step in germination and starts with the uptake of water, also known as imbition. After imbition, enzymes are activated that start to break down starchinto sugars consumed by embryo. The first indication that germination has be-gun is a swelling in the radicle. In onion and pea (Pisum), a structure that looks like a hook goes up through the soil and expose cotyledons and both hypocotyl and epicotyl (first internode). In beans, grasses, and palms, only epicotyl is ex-posed aboveground whereas cotyledons and hypocotyl remain underground.
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