Vascular tissue is an important adaptation to life on land.
It enables the transport of water and nutrients.
Seeds evolved to protect and nourish the sporophyte embryo.
The sporophyte is the dominant and independent stage in vascular plants.
Xylem transports water through tracheids.
Vascular plants are also known as "tracheophytes" because of this.
Cell walls are fortified with the polymer lignin.
Phloem transports sugars.
Rhyniophytes had a "protostele" organization, with phloem surrounding xylem.
Rhyniophytes were the first vascular plants.
They possessed sporangia.
Larger, more complex plants evolved branching.
The first branching was dichotomous, not apical.
Extant tracheophytes possess leaves and roots unlike Rhyniophytes.
Rhyniophytes had an underground stem.
Origin of plants: approximately 470 million years ago (mya).
Origin of vascular plants: approximately 425 mya.
Origin of seed plants: approximately 360 mya.
Lycophytes and Monilophytes diverged before the origin of seed plants.
Nonvascular plants (bryophytes): Liverworts, Mosses, Hornworts.
Seedless vascular plants: Lycophytes (club mosses, spikemosses, quillworts), Monilophytes (ferns, horsetails, whisk ferns).
Seed plants: Gymnosperms, Angiosperms.
Have roots and small leaves.
Leaves of lycophytes are not homologous to leaves of ferns and seed plants.
Lycophytes have microphylls.
Monilophytes, gymnosperms, and angiosperms have megaphylls.
Lycophytes evolved a heterosporous life cycle in some lineages.
Homosporous spore production (most seedless vascular plants):
Sporangium on sporophyll produces a single type of spore.
The spore develops into a typically bisexual gametophyte.
The gametophyte produces both eggs and sperm.
Heterosporous spore production (all seed plants):
Megasporangium on megasporophyll produces megaspores, which develop into female gametophytes that produce eggs.
Microsporangium on microsporophyll produces microspores, which develop into male gametophytes that produce sperm.
Selaginella kraussiana has a strobilus with megasporangia containing megaspores and microsporangia containing microspores.
Some lycophyte lineages evolved secondary growth analogous to that seen in seed plants.
Wood Growth and Structure:
Key components include outer bark, latewood, earlywood, pith, sapwood, phloem, cambium, and heartwood.
Lycophyte "trees" once dominated the world.
As with lycophytes, the dominant stage is the sporophyte.
The gametophyte is free-living and low to the ground, requiring water for fertilization.
Haploid (n) and Diploid (2n) stages alternate.
Spores are produced by meiosis in the sporangium.
Spores disperse and develop into young gametophytes.
Mature gametophytes possess rhizoids and archegonia on the underside.
Antheridia produce sperm.
Fertilization results in a zygote (2n), which develops into a new sporophyte.
The young sporophyte grows from the gametophyte.
Sporangia are found in sori on the underside of sporophyte leaves (fronds).
Fiddleheads are young leaves.
Homospory is common, but heterospory also evolved in some monilophytes.
Compound megaphylls arise from an underground stem.
Sporophyll is a spore-bearing leaf.
A strobilus (cone) is a branch with densely packed sporophylls.
Strobili can be macroscopic or microscopic.
Homosporous strobili are found in some monilophytes.
Heterosporous lycophytes, such as Selaginella, also possess strobili.
“Euphyllophytes” include ferns and seed plants (plants with megaphylls).
The difference between microphylls and megaphylls is in origin, not necessarily in size.
Monilophytes include Psilotum, which exhibits dichotomous branching, lacks leaves and roots and has terminal sporangia.
Originally thought to be very old but actually an example of convergent evolution.
Monilophytes include Equisetum (horsetail fern).
It's considered a "living fossil" and dominated the prehistoric world with tree-like ancestors.
Large lycophytes, ferns, and equisetum dominated the planet's flora during the Carboniferous Period.
A few tree fern species remain today.
They do not produce seeds.
Lycophytes and monilophytes (ferns) are grouped because they lack the homology of vascular tissue.
They represent an important turning point in the story of land plants.
Vascular tissue allows the sporophyte life stage to grow BIG.
The gametophyte life stage remains small and close to the ground due to the need for water fertilization.
There is a trend of decreasing prominence of the gametophyte life stage.
Haploid populations have “allele filtration” while mutant alleles persist in a diploid population.