Seedless Vascular Plants

Seedless Vascular Plants

Seedless vascular plants, which reproduce and spread through spores, are plants that contain vascular tissue, but do not flower or seed.

Seedless Vascular Plants

The vascular plants, or tracheophytes, are the dominant and most conspicuous group of land plants. They contain tissue that transports water and other substances throughout the plant. More than 260,000 species of tracheophytes represent more than 90 percent of the earth's vegetation. By the late Devonian period, plants had evolved vascular tissue, well-defined leaves, and root systems. With these advantages, plants increased in height and size and were able to spread to all habitats.

Seedless vascular plants are plants that contain vascular tissue, but do not produce flowers or seeds. In seedless vascular plants, such as ferns and horsetails, the plants reproduce using haploid, unicellular spores instead of seeds. The spores are very lightweight (unlike many seeds), which allows for their easy dispersion in the wind and for the plants to spread to new habitats. Although seedless vascular plants have evolved to spread to all types of habitats, they still depend on water during fertilization, as the sperm must swim on a layer of moisture to reach the egg. This step in reproduction explains why ferns and their relatives are more abundant in damp environments, including marshes and rainforests. The life cycle of seedless vascular plants is an alternation of generations, where the diploid sporophyte alternates with the haploid gametophyte phase. The diploid sporophyte is the dominant phase of the life cycle, while the gametophyte is an inconspicuous, but still-independent, organism. Throughout plant evolution, there is a clear reversal of roles in the dominant phase of the life cycle.

Vascular Tissue: Xylem and Phloem

Xylem and phloem form the vascular system of plants to transport water and other substances throughout the plant.

Vascular Tissue: Xylem and Phloem

The first fossils that show the presence of vascular tissue date to the Silurian period, about 430 million years ago. The simplest arrangement of conductive cells shows a pattern of xylem at the center surrounded by phloem. Together, xylem and phloem tissues form the vascular system of plants.

Xylem is the tissue responsible for supporting the plant as well as for the storage and long-distance transport of water and nutrients, including the transfer of water-soluble growth factors from the organs of synthesis to the target organs. The tissue consists of vessel elements, conducting cells, known as tracheids, and supportive filler tissue, called parenchyma. These cells are joined end-to-end to form long tubes. Vessels and tracheids are dead at maturity. Tracheids have thick secondary cell walls and are tapered at the ends. It is the thick walls of the tracheids that provide support for the plant and allow it to achieve impressive heights. Tall plants have a selective advantage by being able to reach unfiltered sunlight and disperse their spores or seeds further away, thus expanding their range. By growing higher than other plants, tall trees cast their shadow on shorter plants and limit competition for water and precious nutrients in the soil. The tracheids do not have end openings like the vessels do, but their ends overlap with each other, with pairs of pits present. The pit pairs allow water to pass horizontally from cell to cell.

Phloem tissue is responsible for translocation, which is the transport of soluble organic substances, for example, sugar. The substances travel along sieve elements, but other types of cells are also present: the companion cells, parenchyma cells, and fibers. The end walls, unlike vessel members in xylem, do not have large openings. The end walls, however, are full of small pores where cytoplasm extends from cell to cell. These porous connections are called sieve plates. Despite the fact that their cytoplasm is actively involved in the conduction of food materials, sieve-tube members do not have nuclei at maturity. The activity of the sieve tubes is controlled by companion cells through plasmadesmata.

The Evolution of Roots in Seedless Plants

Roots support plants by anchoring them to soil, absorbing water and minerals, and storing products of photosynthesis.

Roots: Support for the Plant

Roots are not well preserved in the fossil record. Nevertheless, it seems that roots appeared later in evolution than vascular tissue. The development of an extensive network of roots represented a significant new feature of vascular plants. Roots provided seed plants with three major functions: anchoring the plant to the soil, absorbing water and minerals and transporting them upwards, and storing the products of photosynthesis. Importantly, roots are modified to absorb moisture and exchange gases. In addition, while most roots are underground, some plants have adventitious roots, which emerge above the ground from the shoot.

Types of Root Systems

There are mainly two types of root systems. Dicots (flowering plants with two embryonic seed leaves) have a tap root system while monocots (flowering plants with one embryonic seed leaf) have a fibrous root system. A tap root system has a main root that grows down vertically from which many smaller lateral roots arise. Dandelions are a good example; their tap roots usually break off when trying to pull these weeds; they can regrow another shoot from the remaining root.

A tap root system penetrates deep into the soil. In contrast, a fibrous root system is located closer to the soil surface, forming a dense network of roots that also helps prevent soil erosion (lawn grasses are a good example, as are wheat, rice, and corn). In addition, some plants actually have a combination of tap root and fibrous roots. Plants that grow in dry areas often have deep root systems, whereas plants growing in areas with abundant water tend to have shallower root systems.

Root Growth and Anatomy

Root growth begins with seed germination. When the plant embryo emerges from the seed, the radicle of the embryo forms the root system. The tip of the root is protected by the root cap, a structure exclusive to roots and unlike any other plant structure. The root cap is continuously replaced because it gets damaged easily as the root pushes through soil. The root tip can be divided into three zones: a zone of cell division, a zone of elongation, and a zone of maturation and differentiation. The zone of cell division is closest to the root tip; it is made up of the actively-dividing cells of the root meristem. The zone of elongation is where the newly-formed cells increase in length, thereby lengthening the root. Beginning at the first root hair is the zone of cell maturation where the root cells begin to differentiate into special cell types. All three zones are in the first centimeter or so of the root tip.

The vascular tissue in the root is arranged in the inner portion of the root, which is called the vascular cylinder. A layer of cells, known as the endodermis, separates the vascular tissue from the ground tissue in the outer portion of the root. The endodermis is exclusive to roots, serving as a checkpoint for materials entering the root's vascular system. A waxy substance called suberin is present on the walls of the endodermal cells. This waxy region, known as the Casparian strip, forces water and solutes to cross the plasma membranes of endodermal cells instead of slipping between the cells. This ensures that only materials required by the root pass through the endodermis, while toxic substances and pathogens are generally excluded. The outermost cell layer of the root's vascular tissue is the pericycle, an area that can give rise to lateral roots. In dicot roots, the xylem and phloem of the stele are arranged alternately in an X shape, whereas in monocot roots, the vascular tissue is arranged in a ring around the pith.

Root Modifications

Root structures may be modified for specific purposes. For example, some roots are bulbous and store starch. Aerial roots and prop roots are two forms of aboveground roots that provide additional support to anchor the plant. Tap roots, such as carrots, turnips, and beets, are examples of roots that are modified for food storage.

Ferns and Other Seedless Vascular Plants

Ferns, club mosses, horsetails, and whisk ferns are seedless vascular plants that reproduce with spores and are found in moist environments.

Ferns and Other Seedless Vascular Plants

Water is required for fertilization of seedless vascular plants; most favor a moist environment. Modern-day seedless tracheophytes include lycophytes and monilophytes.

Phylum Lycopodiophyta: Club Mosses

The club mosses, or phylum Lycopodiophyta, are the earliest group of seedless vascular plants. They dominated the landscape of the Carboniferous, growing into tall trees and forming large swamp forests. Today's club mosses are diminutive, evergreen plants consisting of a stem (which may be branched) and microphylls (leaves with a single unbranched vein). The phylum Lycopodiophyta consists of close to 1,200 species, including the quillworts (Isoetales), the club mosses (Lycopodiales), and spike mosses (Selaginellales), none of which are true mosses or bryophytes.

Lycophytes follow the pattern of alternation of generations seen in the bryophytes, except that the sporophyte is the major stage of the life cycle. The gametophytes do not depend on the sporophyte for nutrients. Some gametophytes develop underground and form mycorrhizal associations with fungi. In club mosses, the sporophyte gives rise to sporophylls arranged in strobili, cone-like structures that give the class its name. Lycophytes can be homosporous or heterosporous.

Phylum Monilophyta: Class Equisetopsida (Horsetails)

Horsetails, whisk ferns, and ferns belong to the phylum Monilophyta, with horsetails placed in the Class Equisetopsida. The single extant genus Equisetum is the survivor of a large group of plants, which produced large trees, shrubs, and vines in the swamp forests in the Carboniferous. The plants are usually found in damp environments and marshes.

The stem of a horsetail is characterized by the presence of joints or nodes, hence the old name Arthrophyta (arthro- = "joint"; -phyta = "plant"). Leaves and branches come out as whorls from the evenly-spaced joints. The needle-shaped leaves do not contribute greatly to photosynthesis, the majority of which takes place in the green stem.

Silica collects in the epidermal cells, contributing to the stiffness of horsetail plants. Underground stems known as rhizomes anchor the plants to the ground. Modern-day horsetails are homosporous and produce bisexual gametophytes.

Phylum Monilophyta: Class Psilotopsida (Whisk Ferns)

While most ferns form large leaves and branching roots, the whisk ferns, Class Psilotopsida, lack both roots and leaves, which were probably lost by reduction. Photosynthesis takes place in their green stems; small yellow knobs form at the tip of the branch stem and contain the sporangia. Whisk ferns were considered an early pterophytes. However, recent comparative DNA analysis suggests that this group may have lost both leaves and roots through evolution and is more closely related to ferns.

Phylum Monilophyta: Class Polypodiopsida (Ferns)

With their large fronds, ferns are the most-readily recognizable seedless vascular plants. More than 20,000 species of ferns live in environments ranging from tropics to temperate forests. Although some species survive in dry environments, most ferns are restricted to moist, shaded places. Ferns made their appearance in the fossil record during the Devonian period and expanded during the Carboniferous.

The dominant stage of the life cycle of a fern is the sporophyte, which typically consists of large compound leaves called fronds. Fronds fulfill a double role; they are photosynthetic organs that also carry reproductive structure. The stem may be buried underground as a rhizome from which adventitious roots grow to absorb water and nutrients from the soil, or they may grow above ground as a trunk in tree ferns. Adventitious organs are those that grow in unusual places, such as roots growing from the side of a stem. Most ferns produce the same type of spores and are, therefore, homosporous. The diploid sporophyte is the most conspicuous stage of the life cycle. On the underside of its mature fronds, sori (singular, sorus) form as small clusters where sporangia develop. Sporangia in a sorus produce spores by meiosis and release them into the air. Those that land on a suitable substrate germinate and form a heart-shaped gametophyte, which is attached to the ground by thin filamentous rhizoids. The inconspicuous gametophyte harbors both sex gametangia. Flagellated sperm are released and swim on a wet surface to where the egg is fertilized. The newly-formed zygote grows into a sporophyte that emerges from the gametophyte, growing by mitosis into the next generation sporophyte.

The Importance of Seedless Vascular Plants

Seedless vascular plants provide many benefits to life in ecosystems, including food and shelter and, to humans, fuel and medicine.

The Importance of Seedless Vascular Plants

Mosses and liverworts are often the first macroscopic organisms to colonize an area, both in a primary succession (where bare land is settled for the first time by living organisms) or in a secondary succession (where soil remains intact after a catastrophic event wipes out many existing species ). Their spores are carried by the wind, birds, or insects. Once mosses and liverworts are established, they provide food and shelter for other species. In a hostile environment, such as the tundra where the soil is frozen, bryophytes grow well because they do not have roots and can dry and rehydrate rapidly once water is again available. Mosses are at the base of the food chain in the tundra biome. Many species, from small insects to musk oxen and reindeer, depend on mosses for food. In turn, predators feed on the herbivores, which are the primary consumers. Some reports indicate that bryophytes make the soil more amenable to colonization by other plants. Because they establish symbiotic relationships with nitrogen-fixing cyanobacteria, mosses replenish the soil with nitrogen.

At the end of the nineteenth century, scientists observed that lichens and mosses were becoming increasingly rare in urban and suburban areas. Since bryophytes have neither a root system for absorption of water and nutrients, nor a cuticle layer that protects them from desiccation, pollutants in rainwater readily penetrate their tissues; they absorb moisture and nutrients through their entire exposed surfaces. Therefore, pollutants dissolved in rainwater penetrate plant tissues readily and have a larger impact on mosses than on other plants. The disappearance of mosses can be considered a bioindicator for the level of pollution in the environment.

Ferns contribute to the environment by promoting the weathering of rock, accelerating the formation of topsoil, and slowing down erosion by spreading rhizomes in the soil. The water ferns of the genus Azolla harbor nitrogen-fixing cyanobacteria and restore this important nutrient to aquatic habitats.

Seedless plants have historically played a role in human life through uses as tools, fuel, and medicine. Dried peat moss, Sphagnum, is commonly used as fuel in some parts of Europe and is considered a renewable resource. Sphagnum bogs are cultivated with cranberry and blueberry bushes. The ability of Sphagnum to hold moisture makes the moss a common soil conditioner. Florists use blocks of Sphagnum to maintain moisture for floral arrangements.

The attractive fronds of ferns make them a favorite ornamental plant. Because they thrive in low light, they are well suited as house plants. More importantly, fiddleheads are a traditional spring food of Native Americans in the Pacific Northwest and are popular as a side dish in French cuisine. The licorice fern, Polypodium glycyrrhiza, is part of the diet of the Pacific Northwest coastal tribes, owing in part to the sweetness of its rhizomes. It has a faint licorice taste and serves as a sweetener. The rhizome also figures in the pharmacopoeia of Native Americans for its medicinal properties and is used as a remedy for sore throat.

By far the greatest impact of seedless vascular plants on human life, however, comes from their extinct progenitors. The tall club mosses, horsetails, and tree-like ferns that flourished in the swampy forests of the Carboniferous period gave rise to large deposits of coal throughout the world. Coal provided an abundant source of energy during the Industrial Revolution, which had tremendous consequences on human societies, including rapid technological progress and growth of large cities, as well as the degradation of the environment. Coal is still a prime source of energy and also a major contributor to global warming.