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Plant Reproduction: Gymnosperms and Angiosperms
Plant Reproduction: Gymnosperms and Angiosperms
Reproduction in Seed Plants
Cones (gymnosperms) and flowers (angiosperms) are specialized structures for sexual reproduction.
These structures are vital for species continuation, analogous to the importance of roots, stems, and leaves for individual plant survival.
Seed plants' life cycles involve alternating diploid sporophyte and haploid gametophyte generations.
Gametophytes produce male and female gametes; their fusion forms a zygote, which develops into the sporophyte generation.
In seed plants, the sporophyte generation is dominant, while the gametophyte generation is reduced and often hidden.
The evolution of cones, flowers, and seeds enabled seed plants to reproduce without dependence on standing water.
This adaptation allows seed plants to thrive in drier terrestrial environments, unlike mosses and ferns.
Life Cycle of Gymnosperms
Gymnosperms like pine trees are diploid sporophytes grown from zygotes within seeds.
Mature pine trees produce male and female cones.
Male cones contain microsporangia that produce male gametophytes called pollen grains.
Female cones contain megasporangia that produce female gametophytes which then produce ovules, where egg cells form.
Wind carries pollen grains from male to female cones.
Pollen grains landing near an ovule may be caught by a sticky secretion.
The pollen grain splits open and grows a pollen tube containing two haploid sperm, should it land near an ovule.
The pollen tube grows into the ovule, delivering the sperm.
One sperm fertilizes the egg to form a zygote; the other sperm disintegrates.
The zygote develops into an embryo within a seed, which also contains a food supply.
Life Cycle of Angiosperms
Angiosperms (flowering plants) are the dominant plant life form on Earth.
Their evolutionary success is attributed to their life cycle, which is independent from standing water for reproduction.
Flowers are evidence of angiosperm success, ensuring plant survival and propagation.
Structure of a Flower
A typical flower produces both male and female gametes, although variations exist.
Some plants have separate male and female flowers on the same plant (e.g., corn).
Others have male and female gametes on separate plants (e.g., willows).
Flowers are modified miniature stems with four types of specialized leaves: sepals, petals, stamens, and carpels.
These leaves are arranged in circles and modified for reproduction.
Sepals and Calyx
The outermost circle consists of sepals, which are often green and leaf-like.
Sepals enclose and protect the flower bud during development.
All sepals together form the calyx.
Petals and Corolla
The second circle consists of petals, which are often brightly colored.
All petals together form the corolla.
Brightly colored petals attract insects and other pollinators.
Sepals and petals are considered sterile leaves because they do not produce gametophytes.
Stamens
Fertile leaves inside the petals contain structures that produce male and female gametophytes.
Stamens form the first circle of fertile leaves.
Each stamen has a filament supporting an anther.
Inside the anther are microsporangia that produce male gametophytes (microspores).
Most angiosperm flowers have multiple stamens.
Carpels and Pistil
Carpels form the centermost circle of flower parts, derived from rolled fertile leaves.
Megasporangia, producing female gametophytes, are located inside these leaves.
A flower may contain one or more carpels, either separate or fused.
One or more carpels form the pistil, consisting of the ovary, style, and stigma.
The ovary is the base, the style is a stalk, and the stigma is at the top of the style.
The stigma receives pollen, often being sticky or having projections to catch it.
For example, the style of a corn plant (corn silk) can be more than 30 centimeters long.
Female Gametophyte
Ovules, containing megasporangia, are located inside each ovary.
A diploid (2N) megaspore mother cell grows inside each ovule.
The megaspore mother cell undergoes meiosis, producing four haploid (N) cells, three of which die.
The remaining haploid cell divides mitotically to produce eight nuclei.
These eight nuclei and their surrounding membrane form the embryo sac, the entire female gametophyte.
The angiosperm female gametophyte is smaller and simpler than those of mosses and ferns.
Inside the embryo sac, two nuclei become polar nuclei in the center, and three nuclei clump at each end.
One of the three nuclei closest to the ovule opening enlarges to become the egg nucleus, flanked by two other nuclei.
The three nuclei at the opposite end of the embryo sac die.
The female gametophyte then contains a female gamete (egg nucleus) ready for fertilization.
Male Gametophyte
The male gametophyte is even smaller than the female gametophyte.
Microsporangia (pollen chambers) inside the anthers produce diploid (2N) microspore mother cells.
Each microspore mother cell divides by meiosis to produce four haploid (N) microspores.
Each microspore becomes a single pollen grain.
The pollen grain wall thickens to protect the contents from dryness and damage.
The pollen grain nucleus undergoes one mitotic division, producing two haploid nuclei: the tube nucleus and the generative nucleus.
The tube nucleus disintegrates, and the generative nucleus divides to form two sperm cells.
The pollen grain (male gametophyte) usually stops growing until deposited on a stigma.
Eventually, the anther dries, its pollen chambers split, and mature pollen grains are released.
Lily flowers demonstrate this process, with anthers ripening, splitting, and exposing mature pollen.
Pollination
Pollination is the transfer of pollen from anther to stigma.
Self-pollination occurs when pollen falls from the anther to the stigma of the same flower.
Most plants cross-pollinate, transferring pollen from one flower to another on a different plant.
Cross-pollination ensures seed formation with pollen from another plant.
Sexual reproduction and cross-pollination increase genetic variation in offspring, enhancing survival and reproduction.
Fertilization
Once a pollen grain lands on a suitable stigma, it grows a pollen tube.
The generative nucleus divides and forms two sperm nuclei.
The pollen tube contains a tube nucleus and two sperm nuclei.
Following a chemical trail, the pollen tube grows down the style, reaches the ovary, and enters the ovule through a small hole.
The sperm nuclei enter the female gametophyte (embryo sac), initiating double fertilization.
Double fertilization occurs only in angiosperms.
One sperm nucleus fuses with the egg nucleus to form the zygote.
The other sperm nucleus fuses with the two polar nuclei, forming the triploid (3N) endosperm.
The endosperm provides food for the embryo.
The endosperm is a nutrient-rich food source for animals, including humans (e.g., corn, wheat, rice).
Fertilization triggers rapid changes in the ovule, ovary, and other flower structures.
The ovule parts toughen to form a seed coat, protecting the embryo and its food supply.
The ovary wall thickens and joins with other parts of the flower stem to become the fruit that holds the seeds.
A fertilized flower produces hormones that direct energy into developing fruits and seeds.
Unfertilized flowers do not produce these hormones, causing them to wither and fall away.
Formation of Seeds
Seed development was a major factor in the success of angiosperms on land.
Seeds nourish and protect delicate embryos.
Angiosperm seeds have either one or two seed leaves called cotyledons.
Cotyledons store food used when the seed germinates.
Monocots (e.g., corn) have one cotyledon.
Dicots (e.g., beans) have two cotyledons.
The epicotyl is the stem length above the cotyledon(s) and develops into the plant's stem, with the apical meristem at its tip.
The hypocotyl is the stem length below the cotyledon(s).
The radicle at the base of the hypocotyl contains the root's apical meristem and becomes the primary root of the plant.
In many plants, the endosperm is almost completely used up by the time the seed is mature, with food stored in large cotyledons (e.g., beans).
In other plants, much endosperm remains in the mature seed (e.g., corn, coconuts).
Coconut "milk" is liquid endosperm, and coconut "meat" is solid endosperm.
In seeds with endosperm, the cotyledons resemble typical leaves.
Seed Coats and Seed Dispersal
Seed coats can be thin and fragile or thick and woody.
Thick seed coats protect seeds from dryness, saltwater, and other adverse conditions.
Tough seed coats protect seeds from animal teeth and digestive chemicals when fruits are eaten.
These seeds often germinate after being dispersed by animals along with digestive wastes, which provide natural fertilizer.
Passing through an animal's digestive system disperses seeds away from the parent plant, reducing competition for resources.
Animals distribute seeds to other areas that may provide suitable environments for survival.
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