Chapter 14b Seed Plants PDF

14.3 Seed Plants: Gymnosperms 333 implemented landscape. FIGURE 14.18 This campus garden was designed by students in the horticulture and landscaping department of the college. (credit: Myriam Feldman) 14.3 Seed Plants: Gymnosperms LEARNING OBJECTIVES By the end of this section, you will be a...

14.3 Seed Plants: Gymnosperms 333 implemented landscape. FIGURE 14.18 This campus garden was designed by students in the horticulture and landscaping department of the college. (credit: Myriam Feldman) 14.3 Seed Plants: Gymnosperms LEARNING OBJECTIVES By the end of this section, you will be able to: Discuss the type of seeds produced by gymnosperms, as well as other characteristics of gymnosperms List the four groups of modern-day gymnosperms and provide examples of each The first plants to colonize land were most likely closely related to modern-day mosses (bryophytes) and are thought to have appeared about 500 million years ago. They were followed by liverworts (also bryophytes) and primitive vascular plants, the pterophytes, from which modern ferns are derived. The life cycle of bryophytes and pterophytes is characterized by the alternation of generations. The completion of the life cycle requires water, as the male gametes must swim to the female gametes. The male gametophyte releases sperm, which must swim—propelled by their flagella—to reach and fertilize the female gamete or egg. After fertilization, the zygote matures and grows into a sporophyte, which in turn will form sporangia, or "spore vessels,” in which mother cells undergo meiosis and produce haploid spores. The release of spores in a suitable environment will lead to germination and a new generation of gametophytes. The Evolution of Seed Plants In seed plants, the evolutionary trend led to a dominant sporophyte generation, in which the larger and more ecologically significant generation for a species is the diploid plant. At the same time, the trend led to a reduction in the size of the gametophyte, from a conspicuous structure to a microscopic cluster of cells enclosed in the tissues of the sporophyte. Lower vascular plants, such as club mosses and ferns, are mostly homosporous (produce only one type of spore). In contrast, all seed plants, or spermatophytes, are heterosporous, forming two types of spores: megaspores (female) and microspores (male). Megaspores develop into female gametophytes that produce eggs, and microspores mature into male gametophytes that generate sperm. Because gametophyte maturation depends on water and nutrient supply from the dominant sporophyte tissue, they are not free-living, as are the gametophytes of seedless vascular plants. Heterosporous seedless plants are seen as the evolutionary forerunners of seed plants. Seeds and pollen—two adaptations to drought—distinguish seed plants from other (seedless) vascular plants. Both adaptations were critical to the colonization of land. Fossils place the earliest distinct seed plants at about 350 million years ago. The earliest reliable record of gymnosperms dates their appearance to the Carboniferous period (359–299 million years ago). Gymnosperms were preceded by the progymnosperms (“first naked seed plants”). This was a transitional group of plants that superficially resembled conifers (“cone bearers”) because they produced wood from the secondary growth of the vascular tissues; however, they still reproduced like ferns, releasing spores to the environment. In the Mesozoic era (251–65.5 million years ago), gymnosperms dominated the landscape. Angiosperms took over by the middle of the Cretaceous period (145.5–65.5 million years ago) in the late Mesozoic era, and have since become the most abundant plant group in most terrestrial biomes. 334 14 Diversity of Plants The two innovative structures of pollen and seed allowed seed plants to break their dependence on water for reproduction and development of the embryo, and to conquer dry land. The pollen grains carry the male gametes of the plant. The small haploid (1n) cells are encased in a protective coat that prevents desiccation (drying out) and mechanical damage. Pollen can travel far from the sporophyte that bore it, spreading the plant’s genes and avoiding competition with other plants. The seed offers the embryo protection, nourishment and a mechanism to maintain dormancy for tens or even thousands of years, allowing it to survive in a harsh environment and ensuring germination when growth conditions are optimal. Seeds allow plants to disperse the next generation through both space and time. With such evolutionary advantages, seed plants have become the most successful and familiar group of plants. Gymnosperms Gymnosperms (“naked seed”) are a diverse group of seed plants and are paraphyletic. Paraphyletic groups do not include descendants of a single common ancestor. Gymnosperm characteristics include naked seeds, separate female and male gametes, pollination by wind, and tracheids, which transport water and solutes in the vascular system. Life Cycle of a Conifer Pine trees are conifers and carry both male and female sporophylls on the same plant. Like all gymnosperms, pines are heterosporous and produce male microspores and female megaspores. In the male cones, or staminate cones, the microsporocytes give rise to microspores by meiosis. The microspores then develop into pollen grains. Each pollen grain contains two cells: one generative cell that will divide into two sperm, and a second cell that will become the pollen tube cell. In the spring, pine trees release large amounts of yellow pollen, which is carried by the wind. Some gametophytes will land on a female cone. The pollen tube grows from the pollen grain slowly, and the generative cell in the pollen grain divides into two sperm cells by mitosis. One of the sperm cells will finally unite its haploid nucleus with the haploid nucleus of an egg cell in the process of fertilization. Female cones, or ovulate cones, contain two ovules per scale. One megasporocyte undergoes meiosis in each ovule. Only a single surviving haploid cell will develop into a female multicellular gametophyte that encloses an egg. On fertilization, the zygote will give rise to the embryo, which is enclosed in a seed coat of tissue from the parent plant. Fertilization and seed development is a long process in pine trees—it may take up to two years after pollination. The seed that is formed contains three generations of tissues: the seed coat that originates from the parent plant tissue, the female gametophyte that will provide nutrients, and the embryo itself. Figure 14.19 illustrates the life cycle of a conifer. Access for free at openstax.org  14.3 Seed Plants: Gymnosperms 335 VISUAL CONNECTION FIGURE 14.19 This image shows the lifecycle of a conifer. At what stage does the diploid zygote form? a. when the female cone begins to bud from the tree b. when the sperm nucleus and the egg nucleus fuse c. when the seeds drop from the tree d. when the pollen tube begins to grow LINK TO LEARNING Watch this video (http://openstax.org/l/gymnosperm) to see the process of seed production in gymnosperms. Diversity of Gymnosperms Modern gymnosperms are classified into four major divisions and comprise about 1,000 described species. Coniferophyta, Cycadophyta, and Ginkgophyta are similar in their production of secondary cambium (cells that generate the vascular system of the trunk or stem) and their pattern of seed development, but are not closely related phylogenetically to each other. Gnetophyta are considered the closest group to angiosperms because they produce true xylem tissue that contains both tracheids and vessel elements. Conifers Conifers are the dominant phylum of gymnosperms, with the most variety of species. Most are tall trees that usually bear scale-like or needle-like leaves. The thin shape of the needles and their waxy cuticle limits water loss through transpiration. Snow slides easily off needle-shaped leaves, keeping the load light and decreasing breaking of branches. These adaptations to cold and dry weather explain the predominance of conifers at high altitudes and in cold climates. Conifers include familiar evergreen trees, such as pines, spruces, firs, cedars, sequoias, and yews (Figure 14.20). A few species are deciduous and lose their leaves all at once in fall. The European larch and the tamarack are examples of deciduous conifers. Many coniferous trees are harvested for paper pulp and timber. The wood of conifers is more primitive than the wood of angiosperms; it contains tracheids, but no vessel elements, and 336 14 Diversity of Plants is referred to as “soft wood.” FIGURE 14.20 Conifers are the dominant form of vegetation in cold or arid environments and at high altitudes. Shown here are the (a) evergreen spruce, (b) sequoia, (c) juniper, and (d) a deciduous gymnosperm: the tamarack Larix laricina. Notice the yellow leaves of the tamarack. (credit b: modification of work by Alan Levine; credit c: modification of work by Wendy McCormac; credit d: modification of work by Micky Zlimen) Cycads Cycads thrive in mild climates and are often mistaken for palms because of the shape of their large, compound leaves. They bear large cones, and unusually for gymnosperms, may be pollinated by beetles, rather than wind. They dominated the landscape during the age of dinosaurs in the Mesozoic era (251–65.5 million years ago). Only a hundred or so cycad species persisted to modern times. They face possible extinction, and several species are protected through international conventions. Because of their attractive shape, they are often used as ornamental plants in gardens (Figure 14.21). FIGURE 14.21 This Encephalartos ferox cycad exhibits large cones. (credit: Wendy Cutler) Access for free at openstax.org  14.3 Seed Plants: Gymnosperms 337 Gingkophytes The single surviving species of ginkgophyte is the Ginkgo biloba (Figure 14.22). Its fan-shaped leaves, unique among seed plants because they feature a dichotomous venation pattern, turn yellow in autumn and fall from the plant. For centuries, Buddhist monks cultivated Ginkgo biloba, ensuring its preservation. It is planted in public spaces because it is unusually resistant to pollution. Male and female organs are found on separate plants. Usually, only male trees are planted by gardeners because the seeds produced by the female plant have an off-putting smell of rancid butter. FIGURE 14.22 This plate from the 1870 book Flora Japonica, Sectio Prima (Tafelband) depicts the leaves and fruit of Gingko biloba, as drawn by Philipp Franz von Siebold and Joseph Gerhard Zuccarini. Gnetophytes Gnetophytes are the closest relatives to modern angiosperms, and include three dissimilar genera of plants. Like angiosperms, they have broad leaves. Gnetum species are mostly vines in tropical and subtropical zones. The single species of Welwitschia is an unusual, low-growing plant found in the deserts of Namibia and Angola. It may live for up to 2000 years. The genus Ephedra is represented in North America in dry areas of the southwestern United States and Mexico (Figure 14.23). Ephedra’s small, scale-like leaves are the source of the compound ephedrine, which is used in medicine as a potent decongestant. Because ephedrine is similar to amphetamines, both in chemical structure and neurological effects, its use is restricted to prescription drugs. Like angiosperms, but unlike other gymnosperms, all gnetophytes possess vessel elements in their xylem. 338 14 Diversity of Plants FIGURE 14.23 Ephedra viridis, known by the common name Mormon tea, grows in the western United States. (credit: US National Park Service, USDA-NRCS PLANTS Database) LINK TO LEARNING Watch this BBC video (http://openstax.org/l/welwitschia) describing the amazing strangeness of Welwitschia. 14.4 Seed Plants: Angiosperms LEARNING OBJECTIVES By the end of this section, you will be able to: Describe the main parts of a flower and their purpose Detail the life cycle of an angiosperm Discuss the two main groups into which flower plants are divided, as well as explain how basal angiosperms differ from others From their humble and still obscure beginning during the early Jurassic period (202–145.5 MYA), the angiosperms, or flowering plants, have successfully evolved to dominate most terrestrial ecosystems. Angiosperms include a staggering number of genera and species; with more than 260,000 species, the division is second only to insects in terms of diversification (Figure 14.24). FIGURE 14.24 These flowers grow in a botanical garden border in Bellevue, WA. Flowering plants dominate terrestrial landscapes. The vivid colors of flowers are an adaptation to pollination by insects and birds. (credit: Myriam Feldman) Angiosperm success is a result of two novel structures that ensure reproductive success: flowers and fruit. Flowers allowed plants to form cooperative evolutionary relationships with animals, in particular insects, to disperse their Access for free at openstax.org  14.4 Seed Plants: Angiosperms 339 pollen to female gametophytes in a highly targeted way. Fruit protect the developing embryo and serve as an agent of dispersal. Different structures on fruit reflect the dispersal strategies that help with the spreading of seeds. Flowers Flowers are modified leaves or sporophylls organized around a central stalk. Although they vary greatly in appearance, all flowers contain the same structures: sepals, petals, pistils, and stamens. A whorl of sepals (the calyx) is located at the base of the peduncle, or stem, and encloses the floral bud before it opens. Sepals are usually photosynthetic organs, although there are some exceptions. For example, the corolla in lilies and tulips consists of three sepals and three petals that look virtually identical—this led botanists to coin the word tepal. Petals (collectively the corolla) are located inside the whorl of sepals and usually display vivid colors to attract pollinators. Flowers pollinated by wind are usually small and dull. The sexual organs are located at the center of the flower. As illustrated in Figure 14.25, the stigma, style, and ovary constitute the female organ, the carpel or pistil, which is also referred to as the gynoecium. A gynoecium may contain one or more carpels within a single flower. The megaspores and the female gametophytes are produced and protected by the thick tissues of the carpel. A long, thin structure called a style leads from the sticky stigma, where pollen is deposited, to the ovary enclosed in the carpel. The ovary houses one or more ovules that will each develop into a seed upon fertilization. The male reproductive organs, the androecium or stamens, surround the central carpel. Stamens are composed of a thin stalk called a filament and a sac-like structure, the anther, in which microspores are produced by meiosis and develop into pollen grains. The filament supports the anther. FIGURE 14.25 This image depicts the structure of a perfect and complete flower. Perfect flowers carry both male and female floral organs. (credit: modification of work by Mariana Ruiz Villareal) Fruit The seed forms in an ovary, which enlarges as the seeds grow. As the seed develops, the walls of the ovary also thicken and form the fruit. In botany, a fruit is a fertilized and fully grown, ripened ovary. Many foods commonly called vegetables are actually fruit. Eggplants, zucchini, string beans, and bell peppers are all technically fruit because they contain seeds and are derived from the thick ovary tissue. Acorns and winged maple keys, whose scientific name is a samara, are also fruit. Mature fruit can be described as fleshy or dry. Fleshy fruit include the familiar berries, peaches, apples, grapes, and 340 14 Diversity of Plants tomatoes. Rice, wheat, and nuts are examples of dry fruit. Another distinction is that not all fruits are derived from the ovary. Some fruits are derived from separate ovaries in a single flower, such as the raspberry. Other fruits, such as the pineapple, form from clusters of flowers. Additionally, some fruits, like watermelon and orange, have rinds. Regardless of how they are formed, fruits are an agent of dispersal. The variety of shapes and characteristics reflect the mode of dispersal. The light, dry fruits of trees and dandelions are carried by the wind. Floating coconuts are transported by water. Some fruits are colored, perfumed, sweet, and nutritious to attract herbivores, which eat the fruit and disperse the tough undigested seeds in their feces. Other fruits have burs and hooks that cling to fur and hitch rides on animals. The Life Cycle of an Angiosperm The adult, or sporophyte, phase is the main phase in an angiosperm’s life cycle. Like gymnosperms, angiosperms are heterosporous. They produce microspores, which develop into pollen grains (the male gametophytes), and megaspores, which form an ovule containing the female gametophytes. Inside the anthers’ microsporangia (Figure 14.26), male microsporocytes divide by meiosis, generating haploid microspores that undergo mitosis and give rise to pollen grains. Each pollen grain contains two cells: one generative cell that will divide into two sperm, and a second cell that will become the pollen tube cell. Access for free at openstax.org  14.4 Seed Plants: Angiosperms 341 VISUAL CONNECTION FIGURE 14.26 This diagram shows the lifecycle of an angiosperm. Anthers and ovaries are structures that shelter the actual gametophytes: the pollen grain and embryo sac. Double fertilization is a process unique to angiosperms. (credit: modification of work by Mariana Ruiz Villareal) If a flower lacked a megasporangium, what type of gamete would it not be able to form? If it lacked a microsporangium, what type of gamete would not form? In the ovules, the female gametophyte is produced when a megasporocyte undergoes meiosis to produce four haploid megaspores. One of these is larger than the others and undergoes mitosis to form the female gametophyte or embryo sac. Three mitotic divisions produce eight nuclei in seven cells. The egg and two cells move to one end of the embryo sac (gametophyte) and three cells move to the other end. Two of the nuclei remain in a single cell and fuse to form a 2n nucleus; this cell moves to the center of the embryo sac. When a pollen grain reaches the stigma, a pollen tube extends from the grain, grows down the style, and enters 342 14 Diversity of Plants through an opening in the integuments of the ovule. The two sperm cells are deposited in the embryo sac. What occurs next is called a double fertilization event (Figure 14.27) and is unique to angiosperms. One sperm and the egg combine, forming a diploid zygote—the future embryo. The other sperm fuses with the diploid nucleus in the center of the embryo sac, forming a triploid cell that will develop into the endosperm: a tissue that serves as a food reserve. The zygote develops into an embryo with a radicle, or small root, and one or two leaf-like organs called cotyledons. Seed food reserves are stored outside the embryo, and the cotyledons serve as conduits to transmit the broken-down food reserves to the developing embryo. The seed consists of a toughened layer of integuments forming the coat, the endosperm with food reserves and, at the center, the well-protected embryo. FIGURE 14.27 Double fertilization occurs only in angiosperms. (credit: modification of work by Mariana Ruiz Villareal) Most flowers carry both stamens and carpels; however, a few species self-pollinate. These are known as “perfect” flowers because they contain both types of sex organs (Figure 14.25. Biochemical and anatomical barriers to self- pollination promote cross-pollination. Self-pollination is a severe form of inbreeding, and can increase the number of genetic defects in offspring. A plant may have perfect flowers, and thus have multiple sexes in each flower; or, it may have imperfect flowers of both kinds on one plant (Figure 14.28). In each case, such species are called monoecious plants, meaning “one house.” Some botanists refer to plants with perfect flowers simply as hermaphroditic. (Note: hermaphrodite is a scientific term for bodies containing two types of sex organs in plants and non-human animals.) Some plants are dioecious, meaning “two houses,” and have male and female flowers (“imperfect flowers”) on different plants. In these species, cross-pollination occurs all the time. FIGURE 14.28 Monoecious plants have both male and female reproductive structures on the same flower or plant. In dioecious plants, males and females reproductive structures are on separate plants. (credit a: modification of work by Liz West; credit c: modification of work by Scott Zona) Access for free at openstax.org  14.4 Seed Plants: Angiosperms 343 Diversity of Angiosperms Angiosperms are classified in a single division, the Anthophyta. Modern angiosperms appear to be a monophyletic group, which means that they originate from a single ancestor. Flowering plants are divided into two major groups, according to the structure of the cotyledons, the pollen grains, and other features: monocots, which include grasses and lilies, and eudicots or dicots, a polyphyletic group. Basal angiosperms are a group of plants that are believed to have branched off before the separation into monocots and eudicots because they exhibit traits from both groups. They are categorized separately in many classification schemes, and correspond to a grouping known as the Magnoliidae. The Magnoliidae group is comprised of magnolia trees, laurels, water lilies, and the pepper family. Basal Angiosperms The Magnoliidae are represented by the magnolias: tall trees that bear large, fragrant flowers with many parts, and are considered archaic (Figure 14.29d). Laurel trees produce fragrant leaves and small inconspicuous flowers. The Laurales are small trees and shrubs that grow mostly in warmer climates. Familiar plants in this group include the bay laurel, cinnamon, spice bush (Figure 14.29a), and the avocado tree. The Nymphaeales are comprised of the water lilies, lotus (Figure 14.29c), and similar plants. All species of the Nymphaeales thrive in freshwater biomes, and have leaves that float on the water surface or grow underwater. Water lilies are particularly prized by gardeners, and have graced ponds and pools since antiquity. The Piperales are a group of herbs, shrubs, and small trees that grow in tropical climates. They have small flowers without petals that are tightly arranged in long spikes. Many species are the source of prized fragrances or spices; for example, the berries of Piper nigrum (Figure 14.29b) are the familiar black pepper that is used to flavor many dishes. FIGURE 14.29 The (a) southern spicebush belongs to the Laurales, the same family as cinnamon and bay laurel. The fruit of (b) the Piper nigrum plant is black pepper, the main product that was traded along spice routes. Notice the small, unobtrusive clustered flowers. (c) Lotus flowers, Nelumbo nucifera, have been cultivated since antiquity for their ornamental value; the root of the lotus flower is eaten as a vegetable. The (d) red berries of a magnolia tree, characteristic of the final stage, are just starting to appear. (credit a: modification of work by Cory Zanker; credit b: modification of work by Franz Eugen Köhler; credit c: modification of work by "berduchwal"/Flickr; credit d: modification of work by "Coastside2"/Wikimedia Commons) Monocots Plants in the monocot group have a single cotyledon in the seedling, and also share other anatomical features. Veins 344 14 Diversity of Plants run parallel to the length of the leaves, and flower parts are arranged in a three- or six-fold symmetry. The pollen from the first angiosperms was monosulcate (containing a single furrow or pore through the outer layer). This feature is still seen in the modern monocots. True woody tissue is rarely found in monocots, and the vascular tissue of the stem is not arranged in any particular pattern. The root system is mostly adventitious (unusually positioned) with no major taproot. The monocots include familiar plants such as the true lilies (not to be confused with the water lilies), orchids, grasses, and palms. Many important crops, such as rice and other cereals (Figure 14.30a), corn, sugar cane, and tropical fruit, including bananas and pineapple, belong to the monocots. FIGURE 14.30 The major crops in the world are flowering plants. One staple food, (a) rice, is a monocot, as are other cereals, while (b) beans are eudicots. Some popular flowers, such as this (c) lily are monocots; while others, such as this (d) daisy are eudicots. (credit a: modification of work by David Nance; credit b: modification of work by USDA, ARS; credit c: modification of work by “longhorndave”/Flickr; credit d: modification of work by “Cellulaer”/NinjaPhoto) Eudicots Eudicots, or true dicots, are characterized by the presence of two cotyledons. Veins form a network in leaves. Flower parts come in four, five, or many whorls. Vascular tissue forms a ring in the stem. (In monocots, vascular tissue is scattered in the stem.) Eudicots can be herbaceous (like dandelions or violets), or produce woody tissues. Most eudicots produce pollen that is trisulcate or triporate, with three furrows or pores. The root system is usually anchored by one main root developed from the embryonic radicle. Eudicots comprise two-thirds of all flowering plants. Many species seem to exhibit characteristics that belong to either group; therefore, the classification of a plant as a monocot or a eudicot is not always clearly evident (Table 14.1). Comparison of Structural Characteristics of Monocots and Eudicots Characteristic Monocot Eudicot Cotyledon One Two Veins in leaves Parallel Network ( branched) Vascular tissue Scattered Arranged in ring pattern Roots Network of adventitious roots Tap root with many lateral roots TABLE 14.1 Access for free at openstax.org  14.4 Seed Plants: Angiosperms 345 Characteristic Monocot Eudicot Pollen Monosulcate Trisulcate Flower parts Three or multiple of three Four, five, multiple of four or five and whorls TABLE 14.1 LINK TO LEARNING Explore this website (http://openstax.org/l/pollinators) for more information on pollinators. The Role of Seed Plants Without seed plants, life as we know it would not be possible. Plants play a key role in the maintenance of terrestrial ecosystems through the stabilization of soils, cycling of carbon, and climate moderation. Large tropical forests release oxygen and act as carbon dioxide “sinks.” Seed plants provide shelter to many life forms, as well as food for herbivores, thereby indirectly feeding carnivores. Plant secondary metabolites are used for medicinal purposes and industrial production. Virtually all animal life is dependent on plants for survival. Animals and Plants: Herbivory Coevolution of flowering plants and insects is a hypothesis that has received much attention and support, especially because both angiosperms and insects diversified at about the same time in the middle Mesozoic. Many authors have attributed the diversity of plants and insects to both pollination and herbivory, or the consumption of plants by insects and other animals. Herbivory is believed to have been as much a driving force as pollination. Coevolution of herbivores and plant defenses is easily and commonly observed in nature. Unlike animals, most plants cannot outrun predators or use mimicry to hide from hungry animals (although mimicry has been used to entice pollinators). A sort of arms race exists between plants and herbivores. To “combat” herbivores, some plant seeds—such as acorn and unripened persimmon—are high in alkaloids and therefore unsavory to some animals. Other plants are protected by bark, although some animals developed specialized mouth pieces to tear and chew vegetal material. Spines and thorns deter most animals, except for mammals with thick fur, and some birds have specialized beaks to get past such defenses. Herbivory has been exploited by seed plants for their own benefit. The dispersal of fruits by herbivorous animals is a striking example of mutualistic relationships. The plant offers to the herbivore a nutritious source of food in return for spreading the plant’s genetic material to a wider area. Animals and Plants: Pollination More than 80 percent of angiosperms depend on animals for pollination (technically the transfer of pollen from the anther to the stigma). Consequently, plants have developed many adaptations to attract pollinators. With over 200,000 different plants dependent on animal pollination, the plant needs to advertise to its pollinators with some specificity. The specificity of specialized plant structures that target animals can be very surprising. It is possible, for example, to determine the general type of pollinators favored by a plant by observing the flower’s physical characteristics. Many bird or insect-pollinated flowers secrete nectar, which is a sugary liquid. They also produce both fertile pollen, for reproduction, and sterile pollen rich in nutrients for birds and insects. Many butterflies and bees can detect ultraviolet light, and flowers that attract these pollinators usually display a pattern of ultraviolet reflectance that helps them quickly locate the flower's center. In this manner, pollinating insects collect nectar while at the same time are dusted with pollen. Large, red flowers with little smell and a long funnel shape are preferred by hummingbirds, who have good color perception, a poor sense of smell, and need a strong perch. White flowers that open at night attract moths. Other animals—such as bats, lemurs, and lizards—can also act as pollinating agents. Any disruption to these interactions, such as the disappearance of bees, for example as a consequence of colony collapse disorders, can lead to disaster for agricultural industries that depend heavily on pollinated crops. The Importance of Seed Plants in Human Life Seed plants are the foundation of human diets across the world. Many societies eat almost exclusively vegetarian 346 14 Diversity of Plants fare and depend solely on seed plants for their nutritional needs. A few crops (rice, wheat, and potatoes) dominate the agricultural landscape. Many crops were developed during the agricultural revolution, when human societies made the transition from nomadic hunter–gatherers to horticulture and agriculture. Cereals, rich in carbohydrates, provide the staple of many human diets. Beans and nuts supply proteins. Fats are derived from crushed seeds, as is the case for peanut and rapeseed (canola) oils, or fruits The medicinal properties of plants have been known to human societies since ancient times. There are references to the use of plants’ curative properties in Egyptian, Babylonian, and Chinese writings from 5,000 years ago. Many modern synthetic therapeutic drugs are derived or synthesized from plant secondary metabolites. Very often, the raw form of the plant or plant-based substance may be unusable even if it demonstrates helpful properties. For example, chaulmoogra oil was somewhat effective for treating leprosy, but it was difficult to apply and painful for patients. In 1915, Alice Ball (at only 23 years old), created a method for extracting the active ester compounds from the oil so that it could be absorbed by the body, creating a much more effective treatment without the negative side effects. The "Ball Technique" remained the preferred method until synthetic medicines replaced it decades later. It is important to note that the same plant extract can be a therapeutic remedy at low concentrations, become an addictive drug at higher doses, and can potentially kill at high concentrations. Table 14.2 presents a few drugs, their plants of origin, and their medicinal applications. Plant Origin of Medicinal Compounds and Medical Applications Plant Compound Application Deadly nightshade ( Atropine Dilate eye pupils for eye exams Atropa belladonna ) Foxglove ( Digitalis Digitalis Heart disease, stimulates heart beat purpurea ) Yam ( Dioscorea Steroids Steroid hormones: contraceptive pill and cortisone spp.) Ephedra ( Ephedra Ephedrine Decongestant and bronchiole dilator spp.) Pacific yew ( Taxus Taxol Cancer chemotherapy; inhibits mitosis brevifolia ) Opium poppy ( Analgesic (reduces pain without loss of consciousness) and narcotic Papaver Opioids (reduces pain with drowsiness and loss of consciousness) in higher doses somniferum ) Quinine tree ( Quinine Antipyretic (lowers body temperature) and antimalarial Cinchona spp.) Salicylic Willow ( Salix spp.) acid Analgesic and antipyretic (aspirin) TABLE 14.2 Access for free at openstax.org