Vascular Tissue: Xylem and Phloem

The first plant 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. Xylem is the tissue responsible for the storage and long-distance transport of water and nutrients, as well as the transfer of water-soluble growth factors from the organs of synthesis to the target organs. The tissue consists of conducting cells, known as tracheids, and supportive filler tissue, called parenchyma. Xylem conductive cells incorporate the compound lignin into their walls, and are thus described as lignified. Lignin itself is a complex polymer: It is impermeable to water and confers mechanical strength on vascular tissue. With their rigid cell walls, the xylem cells provide support to 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 away from the parent plant, thus expanding the species’ range. By growing higher than other plants, tall trees cast their shadows on shorter plants and thereby outcompete them for water and precious nutrients in the soil.

Phloem is the second type of vascular tissue; it transports sugars, proteins, and other solutes throughout the plant. Phloem cells are divided into sieve elements (conducting cells) and cells that support the sieve elements. Together, xylem and phloem tissues form the vascular system of plants ((Figure)).

Figure 1. Vascular bundles in celery. This cross section of a celery stalk shows a number of vascular bundles. The xylem is on the inner part of each bundle. (credit: fir0002 | flagstaffotos.com.au [GFDL 1.2 (http://www.gnu.org/licenses/old-licenses/fdl-1.2.html)], via Wikimedia Commons. Image modified from source.)

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. Thin rhizoids attached bryophytes to the substrate, but these rather flimsy filaments did not provide a strong anchor for the plant; nor did they absorb substantial amounts of water and nutrients. In contrast, roots, with their prominent vascular tissue system, transfer water and minerals from the soil to the rest of the plant. The extensive network of roots that penetrates deep into the soil to reach sources of water also stabilizes plants by acting as a ballast or anchor. The majority of roots establish a symbiotic relationship with fungi, forming mutualistic mycorrhizae, which benefit the plant by greatly increasing the surface area for absorption of water, soil minerals, and nutrients.

Leaves, Sporophylls, and Strobili

A third innovation marks the seedless vascular plants. Accompanying the prominence of the sporophyte and the development of vascular tissue, the appearance of true leaves improved their photosynthetic efficiency. Leaves capture more sunlight with their increased surface area by employing more chloroplasts to trap light energy and convert it to chemical energy, which is then used to fix atmospheric carbon dioxide into carbohydrates. The carbohydrates are exported to the rest of the plant by the conductive cells of phloem tissue.

The existence of two types of leaf morphology—microphylls and megaphylls—suggests that leaves evolved independently in several groups of plants. Microphylls (“little leaves”) are small and have a simple vascular system. The first microphylls in the fossil record can be dated to 350 million years ago in the late Silurian. A single unbranched vein—a bundle of vascular tissue made of xylem and phloem—runs through the center of the leaf. Microphylls may have originated from the flattening of lateral branches, or from sporangia that lost their reproductive capabilities. Microphylls are seen in club mosses. Microphylls probably preceded the development of megaphylls (“big leaves”), which are larger leaves with a pattern of multiple veins. Megaphylls most likely appeared independently several times during the course of evolution. Their complex networks of veins suggest that several branches may have combined into a flattened organ, with the gaps between the branches being filled with photosynthetic tissue. Megaphylls are seen in ferns and more derived vascular plants.

In addition to photosynthesis, leaves play another role in the life of the plants. Pine cones, mature fronds of ferns, and flowers are all sporophylls—leaves that were modified structurally to bear sporangia. Strobili are cone-like structures that contain sporangia. They are prominent in conifers, where they are commonly known as pine cones.

Ferns and Other Seedless Vascular Plants

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. During the Carboniferous period (360 to 300 MYA), swamp forests of club mosses and horsetails—some specimens reaching heights of more than 30 m (100 ft)—covered most of the land. These forests gave rise to the extensive coal deposits that gave the Carboniferous its name. In seedless vascular plants, the sporophyte became the dominant phase of the life cycle.

Water is still required as a medium of sperm transport during the fertilization of seedless vascular plants, and most favor a moist environment. Modern-day seedless tracheophytes include club mosses, horsetails, ferns, and whisk ferns.

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 ((Figure)). 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. Some lycophytes, like the club moss Lycopodium, produce gametophytes that are independent of the sporophyte, developing underground or in other locations where they can form mycorrhizal associations with fungi. In many club mosses, the sporophyte gives rise to sporophylls arranged in strobili, cone-like structures that give the class its name. Sporangia develop within the chamber formed by each sporophyll.

Lycophytes can be homosporous (spores of the same size) or heterosporous (spores of different sizes). The spike moss Selaginella is a heterosporous lycophyte. The same strobilus will contain microsporangia, which produce spores that will develop into the male gametophyte, and megasporangia, which produce spores that will develop into the female gametophyte. Both gametophytes develop within the protective strobilus.

Figure 2. Lycopodium. In the club mosses such as Lycopodium clavatum, sporangia are arranged in clusters called strobili. The generic name means “wolf-foot” from the resemblance of the branched sporophyte to a paw. The specific epithet clavatum refers to the club-shaped strobilus, and reflects the common name of the phylum. (credit: Cory Zanker)

Phylum Monilophyta: Class Equisetopsida (Horsetails)

Horsetails, whisk ferns, and ferns belong to the phylum Monilophyta, with horsetails placed in the class Equisetopsida. The single genus Equisetum is the survivor of a large group of plants, known as Arthrophyta, which produced large trees and entire swamp forests in the Carboniferous. The plants are usually found in damp environments and marshes ((Figure)).

Figure 3. Horsetails. Horsetails, named for the brushy appearance of the sporophyte, thrive in a marsh. (credit: Myriam Feldman)

The stem of a horsetail is characterized by the presence of joints or nodes, hence the 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 ((Figure)).

Figure 4. The jointed stem of a horsetail. Thin leaves originating at the joints are noticeable on the horsetail plant. Because silica deposited in the cell walls made these plants abrasive, horsetails were once used as scrubbing brushes and were nicknamed scouring rushes. (credit: Myriam Feldman)

Silica collected by in the epidermal cells contributes to the stiffness of horsetail plants, but underground stems known as rhizomes anchor the plants to the ground. Modern-day horsetails are homosporous. The spores are attached to elaters—as we have seen, these are coiled threads that spring open in dry weather and casts the spores to a location distant from the parent plants. The spores then germinate to produce small 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, probably lost by reduction. Photosynthesis takes place in their green stems, which branch dichotomously. Small yellow knobs form at the tip of a branch or at branch nodes and contain the sporangia ((Figure)). Spores develop into gametophytes that are only a few millimeters across, but which produce both male and female gametangia. Whisk ferns were considered early pterophytes. However, recent comparative DNA analysis suggests that this group may have lost both vascular tissue and roots through evolution, and is more closely related to ferns.

Figure 5. Psilotum. The whisk fern Psilotum nudum has conspicuous green stems with knob-shaped sporangia. (credit: Forest & Kim Starr)

Phylum Monilophyta: Class Polypodiopsida (True Ferns)

With their large fronds, the true ferns are perhaps the most readily recognizable seedless vascular plants. They are also considered to be the most advanced seedless vascular plants and display characteristics commonly observed in seed plants. More than 20,000 species of ferns live in environments ranging from the 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 (420 MYA) and expanded during the Carboniferous (360 to 300 MYA).

The dominant stage of the life cycle of a fern is the sporophyte, which consists of large compound leaves called fronds. Fronds may be either finely divided or broadly lobed. Fronds fulfill a double role; they are photosynthetic organs that also carry reproductive organs. 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 ((Figure)). Adventitious organs are those that grow in unusual places, such as roots growing from the side of a stem.

Figure 6. A tree fern. Some specimens of this short tree-fern species can grow very tall. (credit: Adrian Pingstone)

The tip of a developing fern frond is rolled into a crozier, or fiddlehead ((Figure)). Fiddleheads unroll as the frond develops.

Figure 7. Fern fiddleheads. Croziers, or fiddleheads, are the tips of fern fronds. (credit a: modification of work by Cory Zanker; credit b: modification of work by Myriam Feldman)

On the underside of each mature fern frond are groups of sporangia called sori ((Figure)a). Most ferns are homosporous. Spores are produced by meiosis and are released into the air from the sporangium. Those that land on a suitable substrate germinate and form a heart-shaped gametophyte, or prothallus, which is attached to the ground by thin filamentous rhizoids ((Figure)b). Gametophytes produce both antheridia and archegonia. Like the sperm cells of other pterophytes, fern sperm have multiple flagella and must swim to the archegonium, which releases a chemoattractant to guide them. The zygote develops into a fern sporophyte, which emerges from the archegonium of the gametophyte. Maturation of antheridia and archegonia at different times encourages cross-fertilization. The full life cycle of a fern is depicted in (Figure).

Figure 8. Fern reproductive stages. Sori (a) appear as small bumps on the underside of a fern frond. (credit: Myriam Feldman). (b) Fern gametophyte and young sporophyte. The sporophyte and gametophyte are labeled. (credit: modification of work by “Vlmastra”/Wikimedia Commons)

Art Connection

Figure 9. Reproductive cycle of a fern. This life cycle of a fern shows alternation of generations with a dominant sporophyte stage. (credit “fern”: modification of work by Cory Zanker; credit “gametophyte”: modification of work by “Vlmastra”/Wikimedia Commons)

Which of the following statements about the fern life cycle is false?

1. Sporangia produce haploid spores.
2. The sporophyte grows from a gametophyte.
3. The sporophyte is diploid and the gametophyte is haploid.
4. Sporangia form on the underside of the gametophyte.

Show Solution

D.

Link to Learning

To see an animation of the life cycle of a fern and to test your knowledge, go to the website.

Career Connection

Landscape Designer

Looking at the ornamental arrangement of flower beds and fountains typical of the grounds of royal castles and historic houses of Europe, it’s clear that the gardens’ creators knew about more than art and design. They were also familiar with the biology of the plants they chose. Landscape design also has strong roots in the United States’ tradition. A prime example of early American classical design is Monticello, Thomas Jefferson’s private estate. Among his many interests, Jefferson maintained a strong passion for botany. Landscape layout can encompass a small private space like a backyard garden, public gathering places such as Central Park in New York City, or an entire city plan like Pierre L’Enfant’s design for Washington, DC.

A landscape designer will plan traditional public spaces—such as botanical gardens, parks, college campuses, gardens, and larger developments—as well as natural areas and private gardens. The restoration of natural places encroached on by human intervention, such as wetlands, also requires the expertise of a landscape designer.

With such an array of necessary skills, a landscape designer’s education should include a solid background in botany, soil science, plant pathology, entomology, and horticulture. Coursework in architecture and design software is also required for the completion of the degree. The successful design of a landscape rests on an extensive knowledge of plant growth requirements such as light and shade, moisture levels, compatibility of different species, and susceptibility to pathogens and pests. Mosses and ferns will thrive in a shaded area, where fountains provide moisture; cacti, on the other hand, would not fare well in that environment. The future growth of individual plants must be taken into account, to avoid crowding and competition for light and nutrients. The appearance of the space over time is also of concern. Shapes, colors, and biology must be balanced for a well-maintained and sustainable green space. Art, architecture, and biology blend in a beautifully designed and implemented landscape ((Figure)).

Figure 10. This landscaped border at a college campus was designed by students in the horticulture and landscaping department of the college. (credit: Myriam Feldman)

The Importance of Seedless 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 plant species. In a hostile environment, like the tundra where the soil is frozen, bryophytes grow well because they do not have roots and can dry and rehydrate quickly once water is again available. Mosses are at the base of the food chain in the tundra biome. Many species—from small herbivorous 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.

By the end of the nineteenth century, scientists had observed that lichens and mosses were becoming increasingly rare in urban and suburban areas. Because bryophytes have neither a root system for absorption of water and nutrients, nor a cuticular layer that protects them from desiccation, pollutants in rainwater readily penetrate their tissues as 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 biological indicator 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 as rhizomes spread throughout 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 with uses as tools, fuel, and medicine. For example, dried peat moss, Sphagnum, is commonly used as fuel in some parts of Europe and is considered a renewable resource. Sphagnum bogs ((Figure)) are cultivated with cranberry and blueberry bushes. In addition, the ability of Sphagnum to hold moisture makes the moss a common soil conditioner. Even florists use blocks of Sphagnum to maintain moisture for floral arrangements!

Figure 11. Sphagnum moss. Sphagnum acutifolium is dried peat moss and can be used as fuel. (credit: Ken Goulding)

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 of bracken fern (Pteridium aquilinum) are a traditional spring food of Native Americans, 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 pharmacopeia 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.