
Definition of a Herb
"The term "herb" also has more than one definition. Botanists describe an herb as a small, seed bearing plant with fleshy, rather than woody, parts (from which we get the term "herbaceous"). In this book, the term refers to a far wider range of plants. In addition to herbaceous perennials, herbs include trees, shrubs, annuals, vines, and more primitive plants, such as ferns, mosses, algae, lichens, and fungi. They [herbs] are valued for their flavor, fragrance, medicinal and healthful qualities, economic and industrial uses, pesticidal properties, and coloring materials (dyes)."
Annual And Biennial Herbs
The twenty-five plants selected for inclusion in this chapter are all annuals, tender annuals, or biennials or perennials best treated as annuals. To save confusion it is better at the outset to define these terms and give general directions as to how each group should be grown, reserving for the individual species any special directions as to culture. Wherever in the list to be given these terms are used, they mean and should be grown in accordance with the following: 1. Annual. A plant living but a single growing season, flowering and fruiting during the summer and fall, and dying when this is accomplished. Their sole means of perpetuation is by their seeds, which may be self-sown, but it is safer to buy fresh seed each year or save your own. The seeds of annuals should be sown where wanted after the danger from frost is over and usually thinned out so that the plants are not too crowded.
3. Biennial. A plant that lives only two years, and generally a headache to most gardeners. It sprouts from seed the first season, but usually does not flower or fruit until the second, after which it dies. Many experienced gardeners sow seeds of biennials every year to save the trouble and uncertainty of wondering when they must be planted in order to survive perma nently. Seeds of biennials should be planted where wanted. Fortunately biennials are rare, but caraway and parsley are among them. |
Perennial Herbs
It has taken several hundred years to reach this degree of competence in the field of medicinal plants. An ocean of non-sense has been drained off the mass of knowledge which these investigators have left to a world eager to know what nature has provided for illness and how we extract it. Scarcely any other scientific achievement has meant so much to medical science, for from it has come such specifics as digitalis, scopolamine, quinine, atropine, morphine, and aconite, to mention only some of the more important. It would be nice to be able to record a similar competence among the herb gardeners. Unhappily they have clung to every rumor of fancied use and persisted in the cultivation of useless weeds centuries after the advocates of their imaginary virtues have been proved completely wrong. Such all-inclusive gullibility, merely for the sake of growing some plant known to be in cultivation at Tours or Cologne or Rome hundreds of years ago, has had one unfortunate effect upon the literature of herb gardening. Although the medical botanists have purged their modern books of plant dross, modern herb books are too often crammed with plants of no medical value and precious little value in cookery. The authors of some of these books, having acquired a smattering of the Latin names of plants, think it incumbent to list all the species of a genus merely because one of them is of unquestioned value. One of these masterly compilations, open before me as I write, lists, under the genus Thymus (thyme), 37 species and varieties, of which only a handful have ever reached this country (most of these being of doubtful value) and only one of which, the true thyme, with its varieties, has any meaning to the modern herb gardener. It is to spare the reader from this avalanche of the superfluous that there has been a drastic selection of the perennial herbs in this chapter. Only 40 are listed, and this number, to some of the more fanatical, may seem very meagre. All strictly medicinal plants have been excluded, and the aim has been to include those of culinary value only, except for a few old garden favorites the cultivation of which has hallowed associations. |
Nonvascular plants are the simplest of all land dwelling plants. Like their closest ancestors, the green algae, they lack an internal means for water transportation. They also do not produce seeds or flowers. They generally only reach a height of one to two centimeters, because they lack the woody tissue necessary for support on land.
Evolutionary History
Scientists possess fossil records that lead them to believe that plants evolved during four distinct periods. Nonvascular plants arose first, during the late Ordovician period of the Paleozoic Era, approximately 460 million years ago. Their closest non plant ancestor is a type of green algae called charophytes. Nonvascular plants exhibit several homologies to charophytes, such as
Scientists also believe that living in shallow water was a preadaptation to living on land. Natural selection probably favored algae (living on the fringes of bodies of water) that could survive through periods when they were not submerged. Waxy cuticles and jacketed organs, both characteristics of nonvascular plants, are possible adaptations that the algae developed to survive in these conditions.
Reproduction
Nonvascular plants can reproduce both sexually and asexually. Asexual reproduction is the less common method. It basically consists of the regeneration of plant material, leaves or other parts, that fall to the ground and generate secondary plants which bear new buds.
Most nonvascular plants, though, reproduce sexually. Their gametes develop within structures called gametangia, which are organs that have protective jackets of sterile cells that prevent the gametes from drying out during development. The male gametangium is called the antheridium, and it produces flagellated sperm. The female gametangium, or archegonium, produces a single egg (ovum). As in algae, the flagellated sperm require water to swim from the antheridium to the archegonium and fertilize the egg. For most species, a film of rainwater or dew is sufficient for fertilization.
Nonvascular plants, along with all other members of the plant world, engage in a life cycle known as alternation of generations. During this cycle, the plant forms both a multicellular diploid generation, the sporophyte, and a multicellular haploid generation, the gametophyte. In nonvascular plants, the dominant generation is the gametophyte, whereas in most plants the sporophyte is dominant. The sporophyte in nonvascular plants is smaller and shorter lived than the gametophyte, and it depends on the gametophyte for survival.
After the sperm swims to the archegonium and fertilizes the egg, the diploid zygote divides by mitosis and develops into an embryonic sporophyte within the archegonium. This sporophyte grows into a long stalk whose base remains attached to the archegonium as the top emerges. A sporangium forms at the tip of the stalk, and haploid spores develop within it by meiosis. Eventually, the sporangium bursts and the spores scatter. They germinate by mitotic division and form structures known as protonema, which eventually develop into mature gametophytes, completing the life cycle.
Habitats
Nonvascular plants are almost always found in damp, shady places. They have little or no resistance to drying, and because they lack vascular tissue they cannot carry water from the ground to the aerial parts of the plant. Like sponges, they must imbibe the water lying on their surfaces and distribute it by the relatively slow means of diffusion, capillary action, and cytoplasmic streaming. Therefore, they cannot survive for very long in areas that are not constantly moist. Some can survive in alternative habitats such as sand dunes, but the majority thrive in dark, dank places. Because of their limited range of terrestrial habitats, nonvascular plants have never dominated much of the earth's landscape.
Energy Acquisition
Like most plants, nonvascular plants acquire energy through photosynthesis. During this process, the plant converts light energy into chemical energy, then proceeds to store it in the form of glucose or other organic compounds. Photosynthesis usually occurs in the upper parts of nonvascular plants, where they produce many small stemlike and leaflike appendages.
Divisions
There are three divisions of nonvascular plants: Bryophyta, Hepatophyta, and Anthocerophyta. Until recently, scientists grouped all three together as one division, Bryophyta, but the current view is that they are probably not related. They do share some key characteristics, such as the presence of a waxy cuticle and gametangia, but they all have distinct characteristics that warrant separate divisions.
Bryophyta
Division Bryophyta consists of the mosses, and it includes approximately 10,000 species. Mosses are the most common and familiar nonvascular plants. They usually grow in a mat formation, which consists of many plants growing in a tight pack to hold one another up. The mat usually has a spongy quality which enables it to retain water, thus aiding in reproduction and preventing the plant from drying out. Mosses possess multicellular, rootlike structures known as rhizoids which they use for attachment and water absorption. All mosses consist of "stems", either branched or unbranched, that bear leaflike structures. It is important to note that these "stems", "roots", and "leaves" are not homologous to those of vascular plants.
In mosses, the capsules of the sporophytes (sporangia) are much more complex than those of the other nonvascular plants. In many cases the sporangia will possess a lid, or operculum, which is separated from the rest of the capsule by a ring. This lid will eventually detach, releasing spores. Spore release is sometimes aided by the movement of peristome teeth, which are arranged radially around the mouth of the capsule.
Hepatophyta
Division Hepatophyta is the home of the liverworts: it contains approximately 6,500 species. These plants differ from mosses in that many do not have their characteristic stem/leaf structure. Instead, their bodies are divided into deeply grooved lobes. Some have coil shaped cells in their sporangia which spring out of the capsule when it opens, helping to disperse the spores. Their capsules are usually much simpler than those of the mosses, consisting of simple spheres that split longitudinally into four sections when mature. Some also develop structures called gemmae, which are bundles of cells that reside in cups on the surface of the plant and are dispersed by raindrops. Their rhizoids are composed of single, elongated cells, not multiple cells as in moss. Anthocerophyta The third and final division, Anthocerophyta, consists of approximately one hundred species of hornworts. These plants resemble liverworts in their gametophytes, but they can be easily distinguished by their sporophytes. Hornworts possess elongated capsules that grow like horns from the gametophytes, arising from a group of cells at the base of the horn that divide continuously throughout the sporophyte's life span. This feature is unique among plants: hornworts are the only known plants to posses a continuously dividing group of cells. Another unique feature of hornworts is their photosynthetic cells: each possess a single large chloroplast instead of the many smaller chloroplasts that most plants have.
Societal Impact
Due to their limited range of habitats, nonvascular plants have not had that great of an impact on society. Because of their sensitivity to the world around them, though, they can be useful indicators of environmental conditions. For example, some mosses are strict calcicoles, and they will only grow where calcium is freely available in the substrate. Nonvascular plants are also particularly susceptible to air and water pollution, which makes them good indicators of the purity of the environment. For example, in the countryside, trees generally have large numbers of mosses and liverworts growing on them, but in towns and cities the trees are generally bare. Mosses are also used in a lot of decorative gardening, and they also serve as food for small animals and insects.
Flowering plants grow in a wide variety of habitats and environments. They can go from germination of a seed to a mature plant producing new seeds in as little as a month or as long as 150 years. Plants that complete their life cycle in a single season are called annuals; while biennials take two years; and perennials may take several to many years to go from germinated seed to producing new seeds. There are two major classes of flowering plants, monocots and dicots—which have been mentioned previously in the leaves and stems tutorials. In order to keep these two classes separate in our minds, let’s take a moment and outline some of the differences between them.
Monocots:
One seed leaf—cotyledon
Flower components in threes or multiples of three
Leaf veins are parallel
No vascular or cork cambiums
Vascular bundles are scattered throughout the stem
One aperture (thin spot) in pollen grains
Dicots:
Two seed leaves—cotyledon
Flower components in four or fives or multiples of fours or fives
Leaf veins are branching and networked
Vascular cambium present, usually cork cambium present
Vascular bundles are arranged in a ring in the stem
Three apertures in pollen grains
Dicots account for slightly under three quarters of all flowering plants. Nearly all flowering trees and shrubs are dicots as well as many annual plants. Monocots include bulb producing plants, grasses, orchids and palms. They are primarily herbaceous, meaning no secondary woody growth.
There are all sorts of flower shapes, sizes, colors and arrangements, however there are a few features that are central to all flowers regardless of their form. A flower starts as an embryonic primordium that develops into a bud and is situation as a specialized branch at the end of a stalk called the peduncle. The receptacle is a small pad-like swollen area on the very top of the peduncle. This serves as the platform for the flower parts. Whorls, which are three or more plant parts, are attached to the receptacle. The sepals are the outermost whorl and are usually green. Sometimes they are confused with leaves. They are usually three to five in number and are collectively referred to as the calyx. The second whorl of flower parts are the petals and are collectively referred to as the corolla. The corolla is usually extra-showy in order to attract pollinators. In wind-pollinated plants the corolla may be missing to maximize pollen exposure to the female flower parts. Just as the sepals in the calyx, the petals in the corolla may be fused together or separate individual units. Nestled inside the two outer whorls are the sexual organs of the flower. The stamens entail the male structures: a semi rigid filament with a sac called the anther dangling from the tip. Pollen grains develop in the anthers (a process which we will discuss in further detail in a later tutorial). Most anthers have slits or pores on the sides to accommodate pollen release. The female organs are collectively referred to as the pistil and includes: a ‘landing pad’ at the top called the stigma, a slender stalk like style that leads down to the swollen base called the ovary. The ovary is what will develop/ripen into a fruit.
As you might have guessed, there are names for the different ways that the flower parts are arranged with respect to the ovary. The ovary is said to be superior if the calyx and corolla are attached to the receptacle at the base of the ovary. However, if the receptacle grows up and around the ovary and the calyx and corolla are attached above it, then the ovary is said to be inferior.
Inside the ovary is an egg-shaped ovule which is held in place within the ovary by means of a short stalk. The ovule is what develops into a seed. Fruits have seeds.
Some flowers are produced all alone, while others are produced in clusters called inflorescences. An inflorescence is characterized by one peduncle with many little stalks serving individual flowers. The little stalks, in this case, are called pedicels and each stalk services one flower.
A fruit is a mature, or ripened, ovary that usually contains seeds. In contrast, a vegetable can consist of leaves (lettuce, cabbage), leaf petioles (celery), specialized leaves (onions), stems (white potato), stems and roots (beets), flowers and their peduncles (broccoli), flower buds (globe artichokes) and or other parts of the plant. A fruit is by definition just the ovary part of a flower, therefore all fruits come exclusively from flowering plants.
A fruit, ripened ovary, has three major regions that are sometimes difficult to distinguish from each other. The outer layer, sometimes referred to as the skin, is actually called the exocarp. The mesocarp is the fleshy portion which is usually eaten when consuming fruit. The endocarp is the innermost boundary around the seed. Sometimes the endocarp is hard and stony such as a peach pit that surrounds the seed. The endocarp can also be papery as in apples, where it is barely visible in cross section. All three of these regions; the exocarp, mesocarp and endocarp, are collectively called the pericarp. The pericarp can be quite thin, as is the case with dry fruits.
Some fruits have flower parts modified or fused to the ovary at maturity. Fruits are classified according to features at maturity: fleshy, dry, split exposing seeds, non-splitting, one ovary or multiple ovaries. We will go through these various classifications and see what examples fall into the various categories.
There are a variety of methods that will get seeds from the ovary to a fertile spot to begin germinating and growing. Not all methods will work for every plant and some plants are very method specific.
The wind can carry light seeds for miles and most seeds and fruits relying on wind dispersal have specialized adaptations. The samaras with their wings and membranes are highly ideal fruits for wind dispersal. Some fruits are too large to be carried in the air, but can be rolled along by the wind. Cottony or woolly hair type adaptations as in the Willow Family, enable better transfer of seeds via the wind. Tumbleweed plants break off and blow along in the wind, all the while dispersing seeds as it bumps along.
There are so many adaptations for the dispersal of seeds by animals that it would take a volume or two to discuss them all. Birds can carry seeds in the mud that they pick up on their feet. Seeds pass through digestive tracts and are deposited randomly by animals. Ants carry collect and carry seeds. Some seeds will not germinate unless they have passed through the acidic environment of a digestive tract. Fur and feathers can trap seeds and some seeds have burrowing type screws or hooks to ensure getting caught on something and carried along.
Some fruits contain trapped air and are thus adapted to dispersal by water. Some pericarps are thick and spongy enough to absorb water slowly and will thus protect the tiny embryo held within. Saltwater dispersed plants generally have these type pericarps and survival requires washing up on a beach somewhere before the saltwater reaches the inside of the seed.
Some fruits mechanically eject fruits, some at a violent velocity. Humans are another method of dispersal whether intentionally or not. Most countries have regulations with regards to bringing fruits and seeds into the country that may harm native species and cultivated crops.
We have been talking about seeds but haven’t really mentioned what a seed is made of and how it becomes a mature plant.
First of all dicot and monocot seeds are different. Recall that a dicot has two seed leaves in the plant embryo, while a monocot has one seed leaf. These seed leaves are called cotyledons. The cotyledons are the food storage organs and will also serve as the first leaves of the growing plant. If you look at a kidney bean—a dicot—you will notice a small white scar on the inner concave edge of the seed, which is called the hilum. The hilum is where the ovule was attached to the ovary wall—analogous to a belly button in a human. The cotyledons are attached to a tiny embryo plant contains the undeveloped leaves and meristematic tissue at one end. The embryo shoot is called the plumule and the cotyledons are attached just beneath the plumule. Above the cotyledons is the stem portion of the axis, and is called the epicotyl. The portion below the cotyledon attachment is called the hypocotyls. The plant embryo is tiny and it will be difficult to see where the stem ends and the root begins. The embryonic root is called the radicle. In some monocots, the radicle and plumule are enclosed for added protection. The tubular sheathing structures are called the coleoptile for the plumule and the coleorhiza for the radicle. At some point the embryonic shoot and root will overtake the protective structures, and the sheathing will cease growing.
Germination is the start of the growing process for a plant embryo. There are a host of internal and external factors that have to be in place in order for germination to occur. Most seeds require some period of dormancy before they will germinate. This can come about by either physiological or mechanical methods or both. Some seeds can break dormancy by scarification which involves artificially cracking the seed coat. In nature, seeds may require a period of freezing and thawing in order to crack the seed coat, or passage through an acidic digestive tract. In most woody plants in temperate regions, a cold period is required before growth will commence. Some plants will absorb vast amounts of water which instigates the activity of enzymes before germination begins. When the seed is water logged oxygen may be reduced and anaerobic respiration may occur until the seed coat cracks and oxygen is admitted to the embryo. In most cases, temperature is vital to germination. Light roles in germination vary depending on the kind of plants involved. Some lettuce seeds, for example, will not germinate in the dark, whereas some seeds such as the California poppy will only germinate in the dark.
This course covers the basis of herbal medicine