Outlines of Lessons in Botany, Part I; From Seed to Leaf
by Jane H. Newell
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I. PLANTS AND THEIR USES 1. Food 2. Clothing 3. Purification of the Air 4. Fuel

II. SEEDLINGS 1. Directions for raising in the Schoolroom 2. Study of Morning-Glory, Sunflower, Bean, and Pea 3. Comparison with other Dicotyledons 4. Nature of the Caulicle 5. Leaves of Seedlings 6. Monocotyledons 7. Food of Seedlings

III. ROOTS 1. Study of the Roots of Seedlings 2. Fleshy Roots 3. Differences between Stem and Root 4. Root-hairs 5. Comparison of a Carrot, an Onion, and a Potato

IV BUDS AND BRANCHES 1. Horsechestnut Magnolia Lilac Beech American Elm Balm of Gilead Tulip-tree Cherry Red Maple Norway Spruce 2. Vernation 3. Phyllotaxy

V STEMS 1. Forms 2. Movements 3. Structure

VI LEAVES 1. Forms and Structure 2. Descriptions 3. Transpiration 4. Assimilation 5. Respiration


In this study, as in all scientific teaching, the teacher's aim should be to foster in his pupils the power of careful observation and clear expression. The actual amount of knowledge gained at school must needs be small, and often quickly forgotten, but the habit of right study is an invaluable possession.

The former method of teaching Botany was confined almost wholly to dry, technical classification. The pupil learned to find the name and order of a plant, but its structure, its habits, its life in short, were untouched by him. We know now that Nature is the best text-book. The pupil should first ask his questions of her and try to interpret her answers; then he may learn with profit what those who better understand her speech have to tell him.

This method of teaching, however, requires much, very much, of the teacher. He must be himself intelligent, well trained, and able to give time to the preparation of his lessons. It seems to us, who are but amateurs, as if it were impossible to teach thus without a thorough comprehension of the whole field. Our own ignorance oppresses us so much that we feel tempted to say that we cannot attempt it. But if the work of leading children to observe the wonders about them is to be done at all, it must be done by us, who are not masters of our subject, and we must find out for ourselves how we can best accomplish this result, since we have so little to guide us.

It is with the hope that the experience of one who has tried to do this with some fair amount of success may be of use to other puzzled experimenters, that I venture to write out some outlines of lessons in Botany for beginners.

The method of beginning with the simpler forms of life is one that appeals to the scientific tendencies of the day. It seems logical to begin with lower forms and work up to the higher. But this method is only suitable for mature minds. We do not teach a child English by showing him the sources of the language; he learns it by daily use. So also the beginning of the study of any Natural Science by the young should be the observation of the most obvious things about them, the things which they can see, and handle, and experiment upon naturally, without artificial aids. Therefore this book concerns itself only with the Flowering Plants.

The author believes that the simplest botanical study should afford the means of identifying plants, as a large part of the student's pleasure in the science will be the recognition of the things about him. The present volume affords the basis for future classification, which Part II, on flowers, will develop. It is, doubtless, as good a way, perhaps the best, to begin with a single plant, and study root, stem, leaves, and flowers as belonging to a whole, but the problem is complicated by practical difficulties. In our climate there are but two months of the school year when flowers are easily obtained. On the other hand, the material for these lessons can be got throughout the winter, and the class, well trained in methodical work, will begin the study of flowers at the season when every day brings some fresh wonder of beauty.

The author will receive gladly any criticisms or suggestions.


175 Brattle St., Cambridge


The lessons here outlined are suitable for children of twelve years of age, and upwards. For younger pupils they would require much adaptation, and even then they would not be so good as some simpler method, such as following the growth of one plant, and comparing it with others at every step. The little ones profit most by describing the very simple things that they see, without much reference to theories.

The outlines follow the plan of Dr. Gray's First Lessons and How Plants Grow, and are intended to be used in connection with either of those books. The necessary references will be found at the end of every section. The book contains also references to a course of interesting reading in connection with the subjects of the lessons.

The lessons may begin, like the text-books, with the subject of Germination, if the seeds are planted before they are required for use, but it is generally preferable to use the first recitation with the class for planting the seeds, in order to have them under the direct care of the pupils. Some general talks about plants are therefore put at the beginning to occupy the time until the seedlings are ready for study.

Some Nasturtiums (Tropaeolum majus) and Morning-Glories should be planted from the first in boxes of earth and allowed to grow over the window, as they are often used for illustrations.



[Footnote 1: This section may be omitted, and the lessons begun with Seedlings, if the teacher prefer.]

What is Botany? The pupils are very apt to say at first that it is learning about flowers. The teacher can draw their attention to the fact that flowers are only a part of the plant, and that Botany is also the study of the leaves, the stem, and the root. Botany is the science of plants. Ask them what the Geranium is. Tell them to name some other plants. The teacher should keep a few growing plants in the schoolroom for purposes of illustration.

Ask them what else there is in the world besides plants. By this question the three kingdoms, animal, vegetable, and mineral, are brought up. It will give occasion for a discussion of the earth and what it contains, the mountains, formed of rocks and soil, the plants growing on the earth, and the animals that inhabit it, including man. Let them name the three kingdoms with some example of each. Which of these kingdoms contain living things? The words organic and inorganic can be brought in here. An organ ([Greek: Ergon], meaning work) is any part that does a special work, as the leaves, the stem of a plant, and the eye, the ear of animals. An organism is a living being made up of such organs. The inorganic world contains the mineral kingdom; the organic world includes the vegetable and animal kingdoms.

One's aim in these lessons should always be to tell the pupils as little as possible. Try to lead them to think out these things for themselves.

Ask them how plants differ from animals. They will say that plants are fixed to one place, while animals can move about; that plants have no will or consciousness, and that animals have. These answers are true when we compare the higher animals with plants, but the differences become lost as we descend in the scale and approach the border land where botanist and zoologist meet on a common ground. Sea-anemones are fixed to the rock on which they grow, while some of the lower plants are able to move from place to place, and it is hardly safe to affirm that a jelly-fish is more conscious of its actions than is a Sensitive Plant, the leaves of which close when the stem is touched.

There is no real division between animals and plants. We try to classify the objects about us into groups, according to the closeness of their relationships, but we must always remember that these hard lines are ours, not Nature's. We attempt, for purposes of our own convenience, to divide a whole, which is so bound together that it cannot be separated into parts that we can confidently place on different sides of a dividing line.

1. Plants as Food-Producers.—The chief distinguishing characteristic of plants is one that the pupils may be led to think out for themselves by asking them what animals feed upon. To help them with this, ask them what they had for breakfast. Oatmeal is mentioned, perhaps. This is made from oats, which is a plant. Coffee and tea, bread made from wheat, potatoes, etc., all come from plants.[1] Beef, butter and milk come from the cow, but the cow lives upon grass. The plant, on the other hand, is nourished upon mineral or inorganic matter. It can make its own food from the soil and the air, while animals can only live upon that which is made for them by plants. These are thus the link between the mineral and animal kingdoms. Ask the scholars if they can think of anything to eat or drink that does not come from a plant. With a little help they will think of salt and water. These could not support life. So we see that animals receive all their food through the vegetable kingdom. One great use of plants is that they are food-producers.

[Footnote 1: Reader in Botany, for use in Schools. Selected and adapted from well-known authors. Ginn & Co., Boston, New York and Chicago, 1889. I. Origin of Cultivated Plants.]

This lesson may be followed by a talk on food and the various plants used for food.[2]

[Footnote 2: The Flour Mills of Minneapolis: Century Magazine, May, 1886. Maize: Popular Science News, Nov. and Dec., 1888.]

2. Clothing.—Plants are used for clothing. Of the four great clothing materials, cotton, linen, silk, and woollen, the first two are of vegetable, the last two of animal origin. Cotton is made from the hairs of the seed of the cotton plant.[1] Linen is made of the inner fibre of the bark of the flax plant. It has been cultivated from the earliest historical times.

[Footnote 1: Reader in Botany. II. The Cotton Plant.]

3. Purification of the Air.—The following questions and experiments are intended to show the pupils, first, that we live in an atmosphere, the presence of which is necessary to support life and combustion (1) and (2); secondly, that this atmosphere is deprived of its power to support life and combustion by the actions of combustion (2), and of respiration (3); thirdly, that this power is restored to the air by the action of plants (4).

We have the air about us everywhere. A so-called empty vessel is one where the contents are invisible. The following experiment is a good illustration of this.

(1) Wrap the throat of a glass funnel with moistened cloth or paper so that it will fit tightly into the neck of a bottle, and fill the funnel with water. If the space between the funnel and the bottle is air-tight, the water will not flow into the bottle.

Do not explain this in advance to the pupils. Ask them what prevents the water from flowing into the bottle. If they are puzzled, loosen the funnel, and show them that the water will now flow in. In the first case, as the air could not escape, the water could not flow in; in the second, the air was displaced by the heavier water.

Ask the pupils why the air in a crowded room becomes so difficult to breathe. Could a person live if he were shut up in an air-tight room for a long time? Fresh air is necessary to life. The teacher may explain that it is the oxygen in the air that supports life. Air is composed one-fifth of this gas and four-fifths of nitrogen. The gases are mixed and the nitrogen simply dilutes the oxygen, as it were.

Fresh air is necessary to support combustion as well as life. Ask them why we put out a fire by throwing a blanket or a rug over it. The following experiment illustrates this.

(2) Take a small, wide-mouthed bottle, covered with a card or cork. To this cover fasten a piece of bent wire with a taper on the end. Light the taper and lower it into the jar. It will burn a few seconds and then go out. Raise and light it again, and it will be extinguished as soon as it is plunged into the bottle. This shows that the oxygen of the air is used up by burning substances, as it is by breathing animals.

The following experiment shows that fire will not burn in an atmosphere of gas from our lungs.

(3) Fill a bottle with gas by breathing into it through a bit of glass tubing, passed through a card or cork, and reaching to the bottom of the bottle. The bottle will be dimmed with moisture, showing the presence of aqueous vapor. A lighted match plunged into the bottle will be immediately extinguished. A better way, which, however, takes some skill in manipulation, is to fill the bottle with water, cover it with a flat piece of glass, and invert the bottle in a dish of water, taking care that no air bubbles enter. Then, through a bit of glass tubing, blow into the bottle till the water is expelled. Cover the mouth with the glass under water, and holding it tightly down, invert the bottle quickly. Set it down, light a match, take away the glass, and at the same instant plunge in the match. If no air has been allowed to enter, the match will go out at once. No animal could live in an atmosphere which could not support combustion.

From these experiments the pupils have seen that the life-sustaining quality of the air is used up by combustion and respiration. To bring in the subject of purification by plants, ask them why all the oxygen in the world is not exhausted by the people and the fires in it. After the subject has been explained, the following experiment can be prepared and put aside till the next lesson.

(4) Fill two bottles with air from the lungs, as in (3) having previously introduced a cutting from a plant into one of the bottles. Allow them to stand in the sun for a day or two. Then test both bottles with a burning match. If properly done, the result will be very striking. The end of the cutting should be in the water of the dish. This experiment will not succeed excepting with bottles such as are used for chemicals, which have their mouths carefully ground. Common bottles allow the air to enter between the bottle and the glass.[1]

[Footnote 1: See note on page 13.]

4. Fuel.—Light a match and allow it to burn until half charred. Blow it out gently, so as to leave a glowing spark. When this spark goes out it will leave behind a light, gray ash. We have to consider the flame, the charred substance, and the ash.

Flame is burning gas. In all ordinary fuels, carbon and hydrogen, in various combinations and free, make the principal part. The first effect of the heat is to set free the volatile compounds of carbon and hydrogen. The hydrogen then begins to unite with the oxygen of the air, forming water, setting free the carbon, which also unites with oxygen, forming carbonic acid gas. The burning gases cause the flame. The following experiment will illustrate this.

(5) Fit a test-tube with a tight cork, through which a bit of glass tubing, drawn out into a jet, is passed, the tubing within being even with the cork. Place some bits of shaving in the tube, cork it, and make the cork perfectly air-tight by coating it with bees wax or paraffine. Heat the test-tube gently over an alcohol lamp. The wood turns black, and vapor issues from the jet, which may be lighted (Fig. 4). Care should be taken to expel all the air before lighting.

(6) That the burning hydrogen forms water by uniting with the oxygen of the air, may be shown by holding a cold glass tumbler over the jet, or over any flame. The glass will be dimmed by drops of moisture.

The charred part of the wood is charcoal, which is one form of carbon. Our ordinary charcoal is made by driving off all the gases from wood, by burning it under cover where only a little air can reach it. The volatile gases burn more readily than the carbon, and are the first substances to be driven off, so that the carbon is left behind nearly pure. In the same way we have driven off all the gases from the half-burned match and left the carbon. The teacher should have a piece of charcoal to show the pupils. It still retains all the markings of the wood.

If the combustion is continued, the carbon also unites with the oxygen of the air, till it is all converted into carbonic acid gas. This was the case with the match where we left the glowing spark. The gray ash that was left behind is the mineral matter contained in the wood.

(7) We can show that this gas is formed by pouring lime water into a bottle in which a candle has been burned as in (2). The water becomes milky from a fine white powder formed by the union of the carbonic acid gas with the lime, forming carbonate of lime. This is a chemical test.

The wood of the match is plainly of vegetable origin; so also is the charcoal, which is nearly pure carbon. Coal is also carbon, the remains of ancient forests, from which the gases have been slowly driven off by heat and pressure. All the common fuels are composed principally of carbon and hydrogen. When these elements unite with oxygen, carbonic acid gas and water are formed.[1]

[Footnote 1: [Transcriber's Note: This note is missing from original text.]]

(8) The same products are formed by respiration. We breathe out carbonic acid gas and water from our lungs. Breathe on a cold glass. It is bedewed exactly as it is by the candle flame. Breathe through a bit of glass tubing into a bottle of lime water. It becomes milky, showing the presence of carbonic acid gas. Why is this?

Every act or thought is accompanied by a consumption of material in the body, which thus becomes unfit for further use. These waste substances, composed chiefly of carbon and hydrogen, unite with oxygen breathed in from the air, forming carbonic acid gas and water, which are breathed out of the system. The action is a process of slow combustion, and it is principally by the heat thus evolved that the body is kept warm. As we are thus constantly taking oxygen from the air, a close room becomes unfit to live in and a supply of fresh air is indispensable. The cycle of changes is completed by the action of plants, which take in carbonic acid gas, use the carbon, and return most of the oxygen to the atmosphere.


[Footnote 1: The glass apparatus required, including an alcohol lamp, may be obtained for one dollar by sending to the Educational Supply Co., No. 6 Hamilton Place, Boston.]

Two small wide-mouthed bottles. A narrow-necked bottle. A glass funnel. A bit of bent glass-tubing. A bit of straight glass-tubing. A flat piece of glass. A test-tube, with jet. An alcohol lamp. A bent wire with taper. A card. A slip of a plant. A dish and pitcher of water. Beeswax or paraffine. Shavings. Lime water. Matches.

Gray's First Lessons. Revised edition. Sect. XVI, 445-7, 437.

How Plants Grow. Chap. III, 279-288.



1. Directions for raising in the Schoolroom.—The seeds should be planted in boxes tilled with clean sand. Plates or shallow crockery pans are also used, but the sand is apt to become caked, and the pupils are likely to keep the seeds too wet if they are planted in vessels that will not drain. The boxes should be covered with panes of glass till the seedlings are well started, and should be kept at a temperature of from 65 deg. to 70 deg. Fahr. It is very important to keep them covered while the seeds are germinating, otherwise the sand will be certain to become too dry if kept in a sufficiently warm place. Light is not necessary, and in winter time the neighborhood of the furnace is often a very convenient place to keep them safe from frost. They should not be in the sun while germinating. When the first sprouts appear above the ground let another set be planted, and so on, till a series is obtained ranging from plants several inches high to those just starting from the seed. The seeds themselves should be soaked for a day and the series is then ready for study. The time required for their growth varies according to the temperature, moisture, etc. Dr. Goodale says they should be ready in ten days.[1]

[Footnote 1: Concerning a few Common Plants, by G.L. Goodale, Boston, D.C. Heath & Co. This little book, which is published, in pamphlet form, for fifteen cents, will be found exceedingly useful.]

I have never been able to raise them so quickly in the schoolroom, nor have the pupils to whom I have given them to plant done so at home. Generally, it is three weeks, at least, before the first specimens are as large as is desirable.

Germinating seeds need warmth, moisture and air. The necessary conditions are supplied in the very best way by growing them on sponge, but it would be difficult to raise enough for a large class in this manner. Place a piece of moist sponge in a jelly-glass, or any glass that is larger at the top, so that the sponge may not sink to the bottom, and pour some water into the glass, but not so much as to touch the sponge. The whole should be covered with a larger inverted glass, which must not be so close as to prevent a circulation of air. The plants can thus be watched at every stage and some should always be grown in this way. The water in the tumbler will keep the sponge damp, and the roots, after emerging from the sponge, will grow well in the moist air. Seeds can also be grown on blotting paper. Put the seeds on several thicknesses of moist blotting paper on a plate, cover them with more moist paper, and invert another plate over them, taking care to allow the free entrance of air.

If possible, it is by far the best way to have the seeds growing in the schoolroom, and make it a regular custom for the pupils to observe them every morning and take notes of their growth.

These lessons on seeds are suitable for pupils of every age, from adults to the youngest children who go to school. The difference should be only in the mode of treatment; but the same principles should be brought out, whatever the age and power of comprehension of the pupil.

For these lessons the following seeds should be planted, according to the above directions:

Morning-Glory, Sunflower or Squash, Bean, Pea, Red Clover, Flax, Corn, Wheat, and Oats.[1] If they can be procured plant also acorns, Pine-seeds, Maple-seeds, and horsechestnuts.

[Footnote 1: A package of these seeds may be obtained for fifty cents, from Joseph Breck & Son, Boston, Mass. They will be sent by mail, postage paid.]

2. Study of Morning-Glory, Sunflower, Bean, and Pea.—For reasons hereafter given, I consider the Morning-Glory the best seedling to begin upon. Having a series, as above described, before them, the pupils should draw the seedlings. When the drawings are made, let them letter alike the corresponding parts, beginning with the plantlet in the seed, and using new letters when a new part is developed. The seed coats need not be lettered, as they do not belong to the plantlet.

After drawing the Morning-Glory series, let them draw the Sunflower or Squash in the same way, then the Bean, and finally the Pea. Let them write answers to the following questions:


[Footnote 1: It has been objected that the Morning-Glory seed is too small to begin upon. If the teacher prefer, he may begin with the Squash, Bean, and Pea. The questions will require but little alteration, and he can take up the Morning-Glory later.]

Tell the parts of the Morning-Glory seed.

What part grows first?

What becomes of the seed-covering?

What appears between the first pair of leaves?

Was this to be seen in the seed?

How many leaves are there at each joint of stem after the first pair?

How do they differ from the first pair?


What are the parts of the seed?

What is there in the Morning-Glory seed that this has not?

How do the first leaves change as the seedling grows?


What are the parts of the seed?

How does this differ from the Morning-Glory seed?

How from the Sunflower seed?

How do the first pair of leaves of the Bean change as they grow?

How many leaves are there at each joint of stem?[1]

[Footnote 1: There are two simple leaves at the next node to the cotyledons; after these there is one compound leaf at each node.]

How do they differ from the first pair?


What are the parts of the seed? Compare it with the Morning-Glory, Sunflower, and Bean.

How does it differ in its growth from the Bean?

What have all these four seeds in common?

What has the Morning-Glory seed that the others have not?

What have the Bean and Pea that the Morning-Glory has not?

How does the Pea differ from all the others in its growth?

What part grows first in all these seeds?

From which part do the roots grow?

What peculiarity do you notice in the way they come up out of the ground?[1]

[Footnote 1: This question refers to the arched form in which they come up. In this way the tender, growing apex is not rubbed.]

The teacher must remember that, unless the pupils have had some previous training, they will first have to learn to use their eyes, and for this they will need much judicious help. They should be assisted to see what is before them, not told what is there. It is absolutely necessary that these questions should be thoroughly understood and correctly answered before any conclusions are drawn from them. For this purpose abundant material is indispensable. It is better not to attempt these lessons on seeds at all, unless there is material enough for personal observation by all the pupils.

After this preliminary work has been done, the names of the parts can be given to the pupils. They may be written under each drawing thus,—ACaulicle;[1] BCotyledons; CRoots; DPlumule. The whole plantlet in the seed is the embryo or germ, whence the sprouting of seeds is called germination.

[Footnote 1: The term radicle is still in general use. The derivation (little root) makes it undesirable. Dr. Gray has adopted caulicle (little stem) in the latest edition of his text-book, which I have followed. Other writers use the term hypocotyl, meaning under the cotyledons.]

I consider this the best order to study the seeds because in the Morning-Glory the cotyledons are plainly leaves in the seed; and in the Squash or Sunflower[2] the whole process is plainly to be seen whereby a thick body, most unlike a leaf, becomes an ordinary green leaf with veins.[3] In the Sunflower the true leaves are nearly the same shape as the cotyledons, so that this is an especially good illustration for the purpose. Thus, without any hint from me, my pupils often write of the Bean, "it has two thick leaves and two thin leaves." In this way the Bean and Pea present no difficulty. The cotyledons in the first make apparently an unsuccessful effort to become leaves, which the second give up altogether.

[Footnote 2: The large Russian Sunflower is the best for the purpose.]

[Footnote 3: These lessons are intended, as has been said, for children over twelve years of age. If they are adapted for younger ones, it is especially important to begin with a seed where the leaf-like character of the cotyledons is evident, or becomes so. Maple is excellent for the purpose. Morning-Glory is too small. Squash will answer very well. I think it characteristic of the minds of little children to associate a term with the first specimen to which it is applied. If the term cotyledon be given them first for those of the Bean and Pea they will say when they come to the Morning-Glory, "but those are leaves, not cotyledons. Cotyledons are large and round." It will be very difficult to make them understand that cotyledons are the first seed-leaves, and they will feel as if it were a forced connection, and one that they cannot see for themselves.]

The teacher's object now is to make the pupils understand the meaning of the answers they have given to these questions. In the first place, they should go over their answers and substitute the botanical terms they have just learned for the ones they have used.


Morning-Glory. A seed covering. Some albumen. Two cotyledons. A caulicle.

Sunflower. An outer covering.[1] An inner covering. Two cotyledons. A caulicle.[2]

[Footnote 1: The so-called seed of Sunflower is really a fruit. The outer covering is the wall of the ovary, the inner the seed-coat. Such closed, one-seeded fruits are called akenes.]

[Footnote 2: The plumule is sometimes visible in the embryo of the Sunflower.]

Bean. A seed covering. Two cotyledons. A caulicle. A plumule.

Pea. The same as the Bean.

They have also learned how the first leaves in the last three differ from those of the Morning-Glory, being considerably thicker in the Sunflower, and very much thicker in the Bean and Pea. Why should the Morning-Glory have this jelly that the others have not? Why do the first leaves of the Sunflower change so much as the seedling grows? What becomes of their substance? Why do those of the Bean shrivel and finally drop off? By this time some bright pupil will have discovered that the baby-plant needs food and that this is stored around it in the Morning-Glory, and in the leaves themselves in the others. It is nourished upon this prepared food, until it has roots and leaves and can make its own living. The food of the Morning-Glory is called albumen; it does not differ from the others in kind, but only in its manner of storage.[1]

[Footnote 1: Reader in Botany. III. Seed-Food.]

Also the questions have brought out the fact that the Bean and Pea have the plumule ready formed in the seed, while the Morning-Glory and Sunflower have not. Why should this be? It is because there is so much food stored in the first two that the plumule can develop before a root is formed, while in the others there is only nourishment sufficient to enable the plantlet to form its roots. These must make the second leaves by their own labor.

3. Comparison with other Dicotyledons.—The pupils should now have other seeds to compare with these four. Let them arrange Flax, Four o-clock, Horsechestnut, Almond, Nasturtium, Maple-seeds, etc., under two heads.

Seeds with the Food stored Seeds with the Food stored outside the plantlet in the embryo itself (Albuminous). (Exalbuminous).

Flax. Four-o'clock. Acorn. Horsechestnut. Almond. Morning-Glory. Maple. Sunflower. Squash. Bean. Pea. Nasturtium.

They may also be divided into those with and without the plumule.

Without Plumule. With Plumule.

Flax. Maple. Sunflower. Acorn. Horsechestnut. Four-o'clock. Almond. Bean. Pea. Morning-Glory. Squash. Nasturtium.

Those with plumules will be seen to have the most abundant nourishment. In many cases this is made use of by man.

These last can be again divided into those in which the cotyledons come up into the air and those where they remain in the ground.

In the Air. In the Ground.

Bean. Almond. Squash. Acorn. Horsechestnut. Pea. Nasturtium.

In the latter the cotyledons are so heavily gorged with nourishment that they never become of any use as leaves. As Darwin points out, they have a better chance of escaping destruction by animals by remaining in the ground.

The cotyledons are very good illustrations of the different uses to which a single organ may be put, and the thorough understanding of it will prepare the pupils' minds for other metamorphoses, and for the theory that all the various parts of a plant are modified forms of a very few members.

4. Nature of the Caulicle.—Probably some of the pupils will have called the caulicle the root. It is, however, of the nature of stem. The root grows only at the end, from a point just behind the tip; the stem elongates throughout its whole length. This can be shown by marking the stem and roots of a young seedling with ink. India ink must be used, as common ink injures the plants. Dip a needle in the ink and prick a row of spots at equal distances on a young root. Corn is very good for this purpose, but Morning-Glory or Bean is better for experiments on the stem. The plants should then be carefully watched and the changes in the relative distance of the spots noted. The experiment is very easily conducted with the seedlings growing on sponge, with their roots in the moist air of the tumbler, as before described.

Dr. Goodale says of this experiment,—"Let a young seedling of corn be grown on damp paper in the manner described in No. 1,[1] and when the longest root is a few centimetres long let it be marked very carefully by means of India ink, or purple ink, put on with a delicate camel's-hair pencil just one centimetre apart. Plants thus marked are to be kept under favorable conditions with respect to moisture and warmth, so that growth will be as rapid as possible. The marks on the older part of the root will not change their relative distance, but the mark at the tip will be carried away from the one next it, showing that the growth has taken place only at this point. Such experiments as the one described are perfectly practicable for all classes of pupils except the very youngest. How far the details of these experiments should be suggested to the pupils, or rather how far they should be left to work out the problem for themselves, is a question to be settled by the teacher in each case. The better plan generally is to bring the problem in a very clear form before the whole class, or before the whole school, and ask whether anybody can think of a way in which it can be solved; for instance, in this case how can it be found out whether roots grow only at their tip or throughout their whole length. If the way is thought out by even a single pupil the rest will be interested in seeing whether the plan will work successfully."

[Footnote 1: Concerning a Few Common Plants, page 25.]

I have been more successful in pricking the roots than in marking them with a brush.

The caulicle can be proved by the manner of its growth to be of the nature of stem, not root. The main root grows from its naked end. Roots can also grow from the sides of the caulicle, as in Indian Corn. In this, it acts precisely as does the stem of a cutting. It can be prettily shown with the seedlings by breaking off a bean at the ground and putting the slip in water. It will throw out roots and the pupil will readily understand that the caulicle does the same thing.

Darwin has made very interesting experiments on the movements of seedlings. If the teacher wishes to repeat some of the experiments he will find the details very fully given in "The Power of Movement of Plants."[1] The pupils can observe in their growing seedlings some of the points mentioned and have already noticed a few in their answers. They have said that the caulicle was the part to grow first, and have spoken of the arched form of the young stem. Their attention should also be drawn to the root-hairs, which are well seen in Corn, Wheat, and Oats. They absorb the liquid food of the plants. A secondary office is to hold the seed firmly, so that the caulicle can enter the ground. This is shown in Red Clover, which may be sown on the surface of the ground. It puts out root-hairs, which attach themselves to the particles of sand and hold the seed. These hairs are treated more fully in the lessons on roots.

[Footnote 1: The Power of Movement in Plants. By Charles Darwin. London. John Murray, 1880.]

[Footnote 1: Reader in Botany. IV. Movements of Seedlings.]

5. Leaves of Seedlings.—Coming now to the question as to the number of leaves at each joint of the stem, the Morning-Glory, Sunflower, and Bean will present no difficulty, but probably all the pupils will be puzzled by the Pea. The stipules, so large and leaf-like, look like two leaves, with a stem between, bearing other opposite leaves, and terminating in a tendril, while in the upper part it could not be told by a beginner which was the continuation of the main stem. For these reasons I left this out in the questions on the Pea, but it should be taken up in the class. How are we to tell what constitutes a single leaf? The answer to this question is that buds come in the axils of single leaves; that is, in the inner angle which the leaf makes with the stem. If no bud can be seen in the Pea, the experiment may be tried of cutting off the top of the seedling plant. Buds will be developed in the axils of the nearest leaves, and it will be shown that each is a compound leaf with two appendages at its base, called stipules, and with a tendril at its apex. Buds can be forced in the same way to grow from the axils of the lower scales, and even from those of the cotyledons, and the lesson may be again impressed that organs are capable of undergoing great modifications. The teacher may use his own judgment as to whether he will tell them that the tendril is a modified leaflet.

6. Monocotyledons.—These are more difficult. Perhaps it is not worth while to attempt to make the pupils see the embryo in Wheat and Oats. But the embryo of Indian Corn is larger and can be easily examined after long soaking. Removing the seed-covering, we find the greater part of the seed to be albumen. Closely applied to one side of this, so closely that it is difficult to separate it perfectly, is the single cotyledon. This completely surrounds the plumule and furnishes it with food from the albumen. There is a line down the middle, and, if we carefully bend back the edges of the cotyledon, it splits along this line, showing the plumule and caulicle within. The plumule consists of successive layers of rudimentary leaves, the outer enclosing the rest (Fig. 10, 1, c). The latter is the first leaf and remains undeveloped as a scaly sheath (Fig. 10, 2, c). In Wheat and Oats the cotyledon can be easily seen in the largest seedlings by pulling off the dry husk of the grain. The food will he seen to have been used up.

The series of Corn seedlings, at least, should be drawn as before and the parts marked, this time with their technical terms. The following questions should then be prepared.


What are the parts of the seed?

Compare these parts with the Morning-Glory, Sunflower, Bean, and Pea.

Where is the food stored?

How many cotyledons have Corn, Wheat, and Oats?

How many have Bean, Pea, Morning-Glory, and Sunflower?

Compare the veins of the leaves of each class and see what difference you can find.

This will bring up the terms dicotyledon and monocotyledon. Di means two, mono means one. This difference in the veins, netted in the first class, parallel in the second, is characteristic of the classes. Pupils should have specimens of leaves to classify under these two heads. Flowering plants are divided first into these two classes, the Dicotyledons and the Monocotyledons.

If Pine-seeds can be planted, the polycotyledonous embryo can also be studied.

7. Food of seedlings.—The food of the Wheat seedling may be shown in fine flour. [1]"The flour is to be moistened in the hand and kneaded until it becomes a homogeneous mass. Upon this mass pour some pure water and wash out all the white powder until nothing is left except a viscid lump of gluten. This is the part of the crushed wheat-grains which very closely resembles in its composition the flesh of animals. The white powder washed away is nearly pure wheat-starch. Of course the other ingredients, such as the mineral matter and the like, might be referred to, but the starch at least should be shown. When the seed is placed in proper soil, or upon a support where it can receive moisture, and can get at the air and still be warm enough, a part of the starch changes into a sort of gum, like that on postage stamps, and finally becomes a kind of sugar. Upon this sirup the young seedling feeds until it has some good green leaves for work, and as we have seen in the case of some plants it has these very early."

[Footnote 1: Concerning a Few Common Plants, page 18.]

The presence of starch can be shown by testing with a solution of iodine. Starch is turned blue by iodine and may thus be detected in flour, in seeds, in potatoes, etc.

After all this careful experimental work the subject may be studied in the text-book and recited, the recitation constituting a thorough review of the whole.

A charming description of the germination of a seed will be found in the Reader. V. The Birth of Picciola.

Gray's Lessons. Sect. II, 8-14. III. How Plants Grow. Sect. I, 22, 23. II.



This subject can be treated more conveniently while the young seedlings are still growing, because their roots are very suitable for study. It seems best, therefore, to take it up before examining the buds.

1. Study of the Roots of Seedlings.—One or two of the seedlings should be broken off and the slips put into a glass of water. They will be studied later. Bean and Sunflower are the best for the purpose.

Begin by telling the pupils to prepare for their first lesson a description of the roots of their seedlings. Those grown on sponge or paper will show the development of the root-hairs, while those grown on sand are better for studying the form of the root. Give them also some fleshy root to describe, as a carrot, or a radish; and a spray of English Ivy, as an example of aerial roots.

Throughout these lessons, the method is pursued of giving pupils specimens to observe and describe before teaching them botanical terms. It is better for them to name the things they see than to find examples for terms already learned. In the first case, they feel the difficulty of expressing themselves and are glad to have the want of exact terms supplied. This method is discouraging at first, especially to the younger ones; but, with time and patience, they will gradually become accustomed to describe whatever they can see. They have, at any rate, used their eyes; and, though they may not understand the real meaning of anything they have seen, they are prepared to discuss the subject intelligently when they come together in the class. If they will first write out their unassisted impressions and, subsequently, an account of the same thing after they have had a recitation upon it, they will be sure to gain something in the power of observation and clear expression. It cannot be too strongly urged that the number of facts that the children may learn is not of the slightest consequence, but that the teacher should aim to cultivate the quick eye, the ready hand, and the clear reason.

The root of the Morning-Glory is primary; it is a direct downward growth from the tip of the caulicle. It is about as thick as the stem, tapers towards the end, and has short and fibrous branches. In some plants the root keeps on growing and makes a tap-root; in the Bean, it soon becomes lost in the branches. These are all simple, that is, there is but one primary root. Sometimes there are several or many, and the root is then said to be multiple. The Pumpkin is an example of this. The root of the Pea is described in the older editions of Gray's Lessons as being multiple, but it is generally simple. Indian Corn, also, usually starts with a single root, but this does not make a tap-root, and is soon followed by many others from any part of the caulicle, or even from the stem above, giving it the appearance of having a multiple root.

The root of the Radish is different from any of these; it is fleshy. Often, it tapers suddenly at the bottom into a root like that of the Morning-Glory with some fibres upon it. It is, in fact, as the Morning-Glory would be if the main root were to be thickened up by food being stored in it. It is a primary tap-root. The radish is spindle-shaped, tapering at top and bottom, the carrot is conical, the turnip is called napiform; some radishes are shaped like the turnip.

The aerial roots of the English Ivy answer another purpose than that of giving nourishment to the plant. They are used to support it in climbing. These are an example of secondary roots, which are roots springing laterally from any part of the stem. The Sweet Potato has both fleshy and fibrous roots and forms secondary roots of both kinds every year.[1] Some of the seedlings will probably show the root-hairs to the naked eye. These will be noticed hereafter.

[Footnote 1: Gray's Lessons, p. 35, Fig. 86.]

It is my experience that pupils always like classifying things under different heads, and it is a good exercise. The following table may be made of the roots they have studied, adding other examples. Dr. Gray says that ordinary roots may be roughly classed into fibrous and fleshy.[1] Thome classes them as woody and fleshy.[2]

[Footnote 1: Gray's Lessons, p. 34.]

[Footnote 2: Text-book of Structural and Physiological Botany. Otto Thome. Translated and edited by Alfred W. Bennett, New York. John Wiley and Sons. 1877. Page 75.]

ROOTS. Primary. Secondary. Fibrous. Fleshy. Roots of cuttings Aerial roots. - Sweet potatoes.[3] Simple. Multiple. Simple.

Morning Glory. Pumpkin Carrot. Sunflower. Radish. Pea. Turnip. Bean. Beet. Corn. Corn.

[Footnote 3: The Irish potato will very likely be mentioned as an example of a fleshy root. The teacher can say that this will be explained later.]

2. Fleshy Roots.—The scholars are already familiar with the storing of food for the seedling in or around the cotyledons, and will readily understand that these roots are storehouses of food for the plant. The Turnip, Carrot, and Beet are biennials; that is, their growth is continued through two seasons. In the first year, they make a vigorous growth of leaves alone, and the surplus food is carried to the root in the form of a syrup, and there stored, having been changed into starch, or something very similar. At the end of the first season, the root is filled with food, prepared for the next year, so that the plant can live on its reserve fund and devote its whole attention to flowering. These roots are often good food for animals. There are some plants that store their surplus food in their roots year after year, using up in each season the store of the former one, and forming new roots continually. The Sweet Potato is an example of this class. These are perennials. The food in perennials, however, is usually stored in stems, rather than in roots, as in trees. Annuals are generally fibrous-rooted, and the plant dies after its first year. The following experiment will serve as an illustration of the way in which the food stored in fleshy roots is utilized for growth.

Cut off the tapering end of a carrot and scoop out the inside of the larger half in the form of a vase, leaving about half of the flesh behind. Put strings through the upper rim, fill the carrot cup with water, and hang it up in a sunny window. Keep it constantly full of water. The leaf-buds below will put forth, and grow into leafy shoots, which, turning upwards, soon hide the vase in a green circle. This is because the dry, starchy food stored in the carrot becomes soft and soluble, and the supply of proper food and the warmth of the room make the leaf-buds able to grow. It is also a pretty illustration of the way in which stems always grow upward, even though there is enough light and air for them to grow straight downwards. Why this is so, we do not know.

3. Differences between the Stem and the Root.—Ask the pupils to tell what differences they have found.

Stems. Roots.

Ascend into the air. Descend into the ground. Grow by a succession of similar Grow only from a point parts, each part when young just behind the tip. elongating throughout. Bear organs. Bear no organs.

There are certain exceptions to the statement that roots descend into the ground; such as aerial roots and parasitic roots. The aerial roots of the Ivy have been mentioned. Other examples of roots used for climbing are the Trumpet Creeper (Tecoma radicans), and the Poison Ivy (Rhus Toxicodendron). Parasitic roots take their food ready-made from the plants into which they strike. The roots of air-plants, such as certain orchids, draw their nourishment from the air.

The experiment of marking roots and stem has been already tried, but it should be repeated. Repetition of experiments is always desirable, as it fixes his conclusions in the pupil's mind. The stem grows by a succession of similar parts, phytomera, each part, or phyton, consisting of node, internode, and leaf. Thus it follows that stems must bear leaves. The marked stems of seedlings show greater growth towards the top of the growing phyton. It is only young stems that elongate throughout. The older parts of a phyton grow little, and when the internode has attained a certain length, variable for different stems and different conditions, it does not elongate at all.

The root, on the contrary, grows only from a point just behind the tip. The extreme tip consists of a sort of cap of hard tissue, called the root-cap. Through a simple lens, or sometimes with the naked eye, it can be distinguished in most of the roots of the seedlings, looking like a transparent tip. "The root, whatever its origin in any case may be, grows in length only in one way; namely, at a point just behind its very tip. This growing point is usually protected by a peculiar cap, which insinuates its way through the crevices of the soil. If roots should grow as stems escaping from the bud-state do,—that is, throughout their whole length—they would speedily become distorted. But, since they grow at the protected tips, they can make their way through the interstices of soil, which from its compactness would otherwise forbid their progress."[1]

[Footnote 1: Concerning a few Common Plants, p. 25.]

The third difference is that, while the stem bears leaves, and has buds normally developed in their axils, roots bear no organs. The stem, however, especially when wounded, may produce buds anywhere from the surface of the bark, and these buds are called adventitious buds. In the same manner, roots occasionally produce buds, which grow up into leafy shoots, as in the Apple and Poplar.[1]

[Footnote 1: See Gray's Structural Botany, p. 29.]

It should be made perfectly clear that the stem is the axis of the plant, that is, it bears all the other organs. Roots grow from stems, not steins from roots, except in certain cases, like that of the Poplar mentioned above. This was seen in the study of the seedling. The embryo consisted of stem and leaves, and the roots were produced from the stem as the seedling grew.

For illustration of this point, the careful watching of the cuttings placed in water will be very instructive. After a few days, small, hard lumps begin to appear under the skin of the stem of the broken seedling Bean. These gradually increase in size until, finally, they rupture the skin and appear as rootlets. Roots are always thus formed under the outer tissues of the stem from which they spring, or the root from which they branch. In the Bean, the roots are in four long rows, quartering the stem. This is because they are formed in front of the woody bundles of the stem, which in the seedling Bean are four. In the Sunflower the roots divide the circumference into six parts. In some of my cuttings of Beans, the stem cracked in four long lines before the roots had really formed, showing the parenchyma in small hillocks, so to speak. In these the gradual formation of the root-cap could be watched throughout, with merely a small lens. I do not know a better way to impress the nature of the root on the pupil's mind. These forming roots might also be marked very early, and so be shown to carry onward their root-cap on the growing-point.

4. Root-hairs. These are outgrowths of the epidermis, or skin of the root, and increase its absorbing power. In most plants they cannot be seen without the aid of a microscope. Indian Corn and Oats, however, show them very beautifully, and the scholars have already noticed them in their seedlings. They are best seen in the seedlings grown on damp sponge. In those grown in sand, they become so firmly united to the particles of soil, that they cannot be separated, without tearing the hairs away from the plant. This will suggest the reason why plants suffer so much from careless transplanting.

The root-hairs have the power of dissolving mineral matters in the soil by the action of an acid which they give out. They then absorb these solutions for the nourishment of the plant. The acid given out was first thought to be carbonic acid, but now it is supposed by some experimenters to be acetic acid, by others to vary according to the plant and the time. The action can be shown by the following experiment, suggested by Sachs.

Cover a piece of polished marble with moist sawdust, and plant some seeds upon it. When the seedlings are somewhat grown, remove the sawdust, and the rootlets will be found to have left their autographs behind. Wherever the roots, with their root-hairs have crept, they have eaten into the marble and left it corroded. The marks will become more distinct if the marble is rubbed with a little vermilion.

In order that the processes of solution and absorption may take place, it is necessary that free oxygen should be present. All living things must have oxygen to breathe, and this gas is as needful for the germination of seeds, and the action of roots and leaves, as it is for our maintenance of life. It is hurtful for plants to be kept with too much water about their roots, because this keeps out the air. This is the reason why house-plants are injured if they are kept too wet.

A secondary office of root-hairs is to aid the roots of seedlings to enter the ground, as we have before noticed.

The root-hairs are found only on the young parts of roots. As a root grows older the root-hairs die, and it becomes of no further use for absorption. But it is needed now for another purpose, as the support of the growing plant. In trees, the old roots grow from year to year like stems, and become large and strong. The extent of the roots corresponds in a general way to that of the branches, and, as the absorbing parts are the young rootlets, the rain that drops from the leafy roof falls just where it is needed by the delicate fibrils in the earth below.[1]

[Footnote 1: Reader in Botany. VI. The Relative Positions of Leaves and Rootlets.]

5. Comparison of a Carrot, an Onion, and a Potato.—It is a good exercise for a class to take a potato, an onion, and a carrot or radish to compare, writing out the result of their observations.

The carrot is a fleshy root, as we have already seen. The onion consists of the fleshy bases of last year's leaves, sheathed by the dried remains of the leaves of former years, from which all nourishment has been drawn. The parallel veining of the leaves is distinctly marked. The stem is a plate at the base, to which these fleshy scales are attached. In the centre, or in the axils of the scales, the newly-forming bulbs can be seen, in onions that are sprouting. If possible, compare other bulbs, as those of Tulip, Hyacinth, or Snowdrop, and the bulb of a Crocus, in which the fleshy part consists of the thickened base of the stem, and the leaves are merely dry scales. This is called a corm.

The potato is a thickened stem. It shows itself to be a stem, because it bears organs. The leaves are reduced to little scales (eyelids), in the axils of which come the buds (eyes). The following delightful experiment has been recommended to me.

In a growing potato plant, direct upwards one of the low shoots and surround it with a little cylinder of stiff carpet paper, stuffed with sphagnum and loam. Cut away the other tuber-disposed shoots as they appear. The enclosed shoot develops into a tuber which stands more or less vertical, and the scales become pretty little leaves. Removing the paper, the tuber and leaves become green, and the latter enlarge a little. A better illustration of the way in which organs adapt themselves to their conditions, and of the meaning of morphology, could hardly be found.

Gray's First Lessons. Sect. v, 65-88. How Plants Grow. Chap. I, 83-90.



1. There is an astonishing amount to be learned from naked branches, and, if pursued in the right way, the study will be found exceedingly interesting. Professor Beal, in his pamphlet on the New Botany,[1] says:—

"Before the first lesson, each pupil is furnished or told where to procure some specimen for study. If it is winter, and flowers or growing plants cannot be had, give each a branch of a tree or shrub; this branch may be two feet long. The examination of these is made during the usual time for preparing lessons, and not while the class is before the teacher. For the first recitation each is to tell what he has discovered. The specimens are not in sight during the recitation. In learning the lesson, books are not used; for, if they are used, no books will contain a quarter of what the pupil may see for himself. If there is time, each member of the class is allowed a chance to mention anything not named by any of the rest. The teacher may suggest a few other points for study. The pupils are not told what they can see for themselves. An effort is made to keep them working after something which they have not yet discovered. If two members disagree on any point, on the next day, after further study, they are requested to bring in all the proofs they can to sustain their different conclusions. For a second lesson, the students review the first lesson, and report on a branch of a tree of another species which they have studied as before. Now they notice any point of difference or of similarity. In like manner new branches are studied and new comparisons made. For this purpose, naked branches of our species of elms, maples, ashes, oaks, basswood, beech, poplars, willows, walnut, butternut, hawthorns, cherries, and in fact any of our native or exotic trees or shrubs are suitable. A comparison of the branches of any of the evergreens is interesting and profitable. Discoveries, very unexpected, are almost sure to reward a patient study of these objects. The teacher must not think time is wasted. No real progress can be made, till the pupils begin to learn to see; and to learn to see they must keep trying to form the habit from the very first; and to form the habit they should make the study of specimens the main feature in the course of training."

[Footnote 1: The New Botany. By W.J. Beal. Philadelphia, C.H. Marot, 814 Chestnut St., 1882. Page 5.]

HORSECHESTNUT (AEsculus Hippocastanum).

We will begin with the study of a branch of Horsechestnut.[1] The pupils should examine and describe their specimens before discussing them in the class-room. They will need some directions and hints, however, to enable them to work to any advantage. Tell them to open both large and small buds. It is not advisable to study the Horsechestnut bud by cutting sections, as the wool is so dense that the arrangement cannot be seen in this way. The scales should be removed with a knife, one by one, and the number, texture, etc., noted. The leaves and flower-cluster will remain uncovered and will be easy to examine. The gum may be first removed by pressing the bud in a bit of paper. The scholars should study carefully the markings on the stem, in order to explain, if possible, what has caused them. The best way to make clear the meaning of the scars is to show them the relation of the bud to the branch. They must define a bud. Ask them what the bud would have become the next season, if it had been allowed to develop. It would have been a branch, or a part of one. A bud, then, is an undeveloped branch. They can always work out this definition for themselves. Conversely, a branch is a developed bud, or series of buds, and every mark on the branch must correspond to something in the bud. Let them examine the specimens with this idea clearly before their minds. The lesson to prepare should be to write out all they can observe and to make careful drawings of their specimens. Ask them to find a way, if possible, to tell the age of the branch.

[Footnote 1: The pupils should cut their names on their branches and keep them. They will need them constantly for comparison and reference.]

At the recitation, the papers can be read and the points mentioned thoroughly discussed. This will take two lesson-hours, probably, and the drawing may be left, if desired, as the exercise to prepare for the second recitation.

[1]The buds of Horsechestnut contain the plan of the whole growth of the next season. They are scaly and covered, especially towards the apex, with a sticky varnish. The scales are opposite, like the leaves. The outer pairs are wholly brown and leathery, the succeeding ones tipped with brown, wherever exposed, so that the whole bud is covered with a thick coat. The inner scales are green and delicate, and somewhat woolly, especially along the lapping edges. There are about seven pairs of scales. The larger terminal buds have a flower-cluster in the centre, and generally two pairs of leaves; the small buds contain leaves alone, two or three pairs of them. The leaves are densely covered with white wool, to protect them from the sudden changes of winter. The use of the gum is to ward off moisture. The flower-cluster is woolly also.

[Footnote 1: All descriptions are made from specimens examined by me. Other specimens may differ in some points. Plants vary in different situations and localities.]

The scars on the stem are of three kinds, leaf, bud-scale, and flower-cluster scars. The pupils should notice that the buds are always just above the large triangular scars. If they are still in doubt as to the cause of these marks, show them some house-plant with well-developed buds in the axils of the leaves, and ask them to compare the position of these buds with their branches. The buds that spring from the inner angle of the leaf with the stem are axillary buds; those that crown the stems are terminal. Since a bud is an undeveloped branch, terminal buds carry, on the axis which they crown, axillary buds give rise to side-shoots. The leaf-scars show the leaf-arrangement and the number of leaves each year. The leaves are opposite and each pair stands over the intervals of the pair below. The same is observed to be true of the scales and leaves of the bud.[1] All these points should be brought out by the actual observation of the specimens by the pupils, with only such hints from the teacher as may be needed to direct their attention aright. The dots on the leaf-scar are the ends of woody bundles (fibro-vascular bundles) which, in autumn, separated from the leaf. By counting these we can tell how many leaflets there were in the leaf, three, five, seven, nine, or occasionally six or eight.

[Footnote 1: Bud-scales are modified leaves and their arrangement is therefore the same as the leaves. This is not mentioned in the study of the Horsechestnut bud, because it cannot be proved to the pupils, but the transition is explained in connection with Lilac, where it may be clearly seen. The scales of the bud of Horsechestnut are considered to be homologous with petioles, by analogy with other members of the same family. In the Sweet Buckeye a series can be made, exhibiting the gradual change from a scale to a compound leaf. See the Botanical Text-Book, Part I, Structural Botany. By Asa Gray. Ivison, Blakeman, Taylor and Co., New York, 1879. Plate 233, p. 116.]

The Bud Scale-Scars. These are rings left by the scales of the bud and may be seen in many branches. They are well seen in Horsechestnut. If the pupils have failed to observe that these rings show the position of former buds and mark the growth of successive years, this point must be brought out by skilful questioning. There is a difference in the color of the more recent shoots, and a pupil, when asked how much of his branch grew the preceding season, will be able to answer by observing the change in color. Make him see that this change corresponds with the rings, and he will understand how to tell every year's growth. Then ask what would make the rings in a branch produced from one of his buds, and he can hardly fail to see that the scales would make them. When the scholars understand that the rings mark the year's growth, they can count them and ascertain the age of each branch. The same should be done with each side-shoot. Usually the numbers will be found to agree; that is, all the buds will have the same number of rings between them and the cut end of the branch, but occasionally a bud will remain latent for one or several seasons and then begin its growth, in which case the numbers will not agree; the difference will be the number of years it remained latent. There are always many buds that are not developed. "The undeveloped buds do not necessarily perish, but are ready to be called into action in case the others are checked. When the stronger buds are destroyed, some that would else remain dormant develop in their stead, incited by the abundance of nourishment which the former would have monopolized. In this manner our trees are soon reclothed with verdure, after their tender foliage and branches have been killed by a late vernal frost, or consumed by insects. And buds which have remained latent for several years occasionally shoot forth into branches from the sides of old stems, especially in certain trees."[1]

[Footnote 1: Structural Botany, p. 48.]

The pupils can measure the distance between each set of rings on the main stem, to see on what years it grew best.

The Flower-Cluster Scars. These are the round, somewhat concave, scars, found terminating the stem where forking occurs, or seemingly in the axils of branches, on account of one of the forking branches growing more rapidly and stoutly than the other and thus taking the place of the main stem, so that this is apparently continued without interruption. If the pupils have not understood the cause of the flower-cluster scars, show them their position in shoots where they are plainly on the summit of the stem, and tell them to compare this with the arrangement of a large bud. The flower-cluster terminates the axis in the bud, and this scar terminates a branch. When the terminal bud is thus prevented from continuing its growth, the nearest axillary buds are developed.[1] One shoot usually gets the start, and becomes so much stronger that it throws the other to one side. The tendency of the Horsechestnut to have its growth carried on by the terminal buds is so strong that I almost feel inclined to say that vigorous branches are never formed from axillary buds, in old trees, except where the terminal bud has been prevented from continuing the branch. This tendency gives to the tree its characteristic size of trunk and branches, and lack of delicate spray. On looking closely at the branches also, they will be seen to be quite irregular, wherever there has been a flower-cluster swerving to one side or the other.

[Footnote 1: The first winter that I examined Horsechestnut buds I found, in many cases, that the axillary shoots had from a quarter of an inch to an inch of wood before the first set of rings. I could not imagine what had formed this wood, and it remained a complete puzzle to me until the following spring, when I found in the expanding shoots, that, wherever a flower-cluster was present, there were one or two pairs of leaflets already well developed in the axils, and that the next season's buds were forming between them, while the internodes of these leaflets were making quite a rapid growth. Subsequently, I found the leaflets also in the buds themselves. I found these leaflets developed on the tree only in the shoots containing flower-clusters, where they would be needed for the future growth of the branches. I suppose the reason must be that the flower-cluster does not use all the nourishment provided and that therefore the axillary buds are able to develop. It would be interesting to know what determines the stronger growth of the one which eventually becomes the leader.]

There is one thing more the pupils may have noticed. The small round dots all over the young stem, which become long rifts in the older parts, are breaks in the epidermis, or skin of the stem, through which the inner layers of bark protrude. They are called lenticels. They provide a passage for gases in and out of the stem. In some trees, as the Birch, they are very noticeable.

After discussing the subject thoroughly in the class-room, the pupils should rewrite their papers, and finally answer the following questions, as a species of review. I have thus spent three recitations on the Horsechestnut. The work is all so new, and, if properly presented, so interesting, that a good deal of time is required to exhaust its possibilities of instruction. If the teacher finds his scholars wearying, however, he can leave as many of the details as he pleases to be treated in connection with other branches.


How many scales are there in the buds you have examined?

How are they arranged?

How many leaves are there in the buds?

How are they arranged?

Where does the flower-cluster come in the bud?

Do all the buds contain flower-clusters?

What is the use of the wool and the gum?

Where do the buds come on the stem?

Which are the strongest?

How are the leaves arranged on the stem?

Do the pairs stand directly over each other?

What are the dots on the leaf-scars?

How old is your branch?

How old is each twig?

Which years were the best for growth?

Where were the former flower-clusters?

What happens when a branch is stopped in its growth by flowering?

What effect does this have on the appearance of the tree?

In some parts of the country the Horsechestnut is not so commonly planted as in New England. In the southern states the Magnolia may be used in its stead, but it is not nearly so simple an example of the main points to be observed.[1]

[Footnote 1: Reader in Botany. VII. Trees in Winter.]


The bud may be examined by removing the scales with a knife, as in Horsechestnut, and also by cutting sections. The outer scales enfold the whole bud, and each succeeding pair cover all within. They are joined, and it is frequently difficult to tell where the suture is, though it can generally be traced at the apex of the bud. On the back is a thick stalk, which is the base of the leaf-stalk. Remove the scales by cutting carefully through a single pair, opposite the leaf-stalk, and peeling them off. The scales are modified stipules, instead of leaf-stalks, as in Horsechestnut. The outer pair are brown and thick, the inner green, and becoming more delicate and crumpled as we proceed toward the centre of the bud. The leaves begin with the second or third pair of scales. The first one or two are imperfect, being small, brown, and dry. The leaves grow larger towards the centre of the bud. They are covered with short, silky hairs, and are folded lengthwise, with the inner surface within (conduplicate). In the specimens I have examined I do not see much difference in size between the buds with flowers and those without. In every bud examined which contained a flower, there was an axillary bud in the axil of the last, or next to the last, leaf. This bud is to continue the interrupted branch in the same way as in Horsechestnut.

There are from six to ten good leaves, in the buds that I have seen. Those without flowers contain more leaves, as in Horsechestnut. In the centre of these buds the leaves are small and undeveloped. The flower is very easy to examine, the floral envelopes, stamens and pistils, being plainly discernible. The bud may also be studied in cross-section. This shows the whole arrangement. The plan is not so simple as in Horsechestnut, where the leaves are opposite. The subject of leaf-arrangement should be passed over until phyllotaxy is taken up.

The scars on the stem differ from Horsechestnut in having no distinct bands of rings. The scales, being stipules, leave a line on each side of the leaf-scar, and these are separated by the growth of the internodes. In the Beech, the scales are also stipules; but, whereas in the Magnolia there are only one or two abortive leaves, in the Beech there are eight or nine pairs of stipules without any leaves at all. The rings thus become separated in Magnolia, while in the Beech the first internodes are not developed, leaving a distinct band of rings, to mark the season's growth. The Magnolia is therefore less desirable to begin upon. The branches are swollen at the beginning of a new growth, and have a number of leaf-scars crowded closely together. The leaf-scars are roundish, the lower line more curved. They have many dots on them. From each leaf-scar runs an irregular line around the stem. This has been left by the stipules.

The flower-scar is on the summit of the axis, and often apparently in the axil of a branch, as in Horsechestnut. Sometimes the nearest axillary bud is developed; sometimes there are two, when the branch forks. The axillary buds seldom grow unless the terminal bud is interrupted. The tree therefore has no fine spray.

LILAC (Syringa vulgaris).

Ask the scholars to write a description of their branches and to compare them with Horsechestnut. These papers should be prepared before coming into the class, as before.

The buds are four-sided. The scales and leaves are opposite, as in Horsechestnut. The outer pair sometimes have buds in their axils. Remove the scales one by one with a knife, or better, with a stout needle. The scales gradually become thinner as we proceed, and pass into leaves, so that we cannot tell where the scales end and leaves begin. After about six pairs are removed, we come, in the larger buds, to leaves with axillary flower-clusters. The leaves grow smaller and the flower-clusters larger till we come to the centre, where the axis is terminated by a flower-cluster. There is a great difference in the buds on different bushes and on shoots of the same bush, some being large, green, and easy to examine, others small, hard, and dark-colored. It is better, of course, to select as soft and large buds as possible for examination.

That the scales are modified leaves is plainly shown by the gradual transition they undergo, and also by the fact that buds are developed in their axils. If any of these can be shown to the pupils, remind them of the experiment where the top of a seedling Pea was cut off and buds forced to develop in the axils of the lower scales.[1] The transition from scales to leaves can be well studied by bringing branches into the house, where they will develop in water, and towards spring may even be made to blossom. Cherry, Apple, Forsythia, and other blossoming trees and shrubs can be thus forced to bloom. Place the branches in hot water, and cut off a little of their ends under water. If the water is changed every day, and the glass kept near the register or stove, they will blossom out very quickly. These expanded shoots may be compared with the buds. The number of leaves in the bud varies.

[Footnote 1: See p. 31.]

The leaf-scars of Lilac are horseshoe-shaped and somewhat swollen. It can often be plainly seen that the outer tissue of the stem runs up into the scar. It looks as if there were a layer of bark, ending with the scar, fastened over each side of the stem. These apparent layers alternate as well as the scars. The epidermis, or skin of the leaves, is in fact always continuous with that of the stem. There are no dots on the leaf-scars.

The rings are not nearly so noticeable as in Horsechestnut, but they can be counted for some years back.

The flower-cluster can often be traced by a dried bit of stem remaining on the branch.

The terminal bud in the Lilac does not usually develop, and the two uppermost axillary buds take its place, giving to the shrub the forked character of its branching. In all these bud studies, the pupil should finish by showing how the arrangement of the buds determines the growth of the branches.


How do the scales differ from those of Horsechestnut?

How many scales and leaves are there?

How are they arranged?

Where does the flower-cluster come in the bud?

Do all the buds contain flower-clusters?

How does the arrangement of leaves and flower-clusters differ from that of Horsechestnut?

How old is your branch?

Which buds develop most frequently?

How does this affect the appearance of the shrub?

COPPER BEECH (Fagus sylvatica, var. purpurea).

The buds are long and tapering, the scales thin and scarious, the outer naked, the inner with long, silky hairs. Remove the scales one by one, as in Lilac. The outer four or six pairs are so minute that the arrangement is not very clear, but as we proceed we perceive that the scales are in alternate pairs, as in Horsechestnut; that is, that two scales are exactly on the same plane. But we have learned in the Lilac that the scales are modified leaves, and follow the leaf-arrangement of the species. The Beech is alternate-leaved, and we should therefore expect the scales to alternate. The explanation is found as we go on removing the scales. At the eighth or ninth pair we come upon a tiny, silky leaf, directly between the pair of scales, and, removing these, another larger leaf, opposite the first but higher up on the rudimentary stem, and so on, with the rest of the bud. There are five or more leaves, each placed between a pair of scales. Our knowledge of the parts of a leaf shows us at once that the scales must be modified stipules, and that therefore they must be in pairs.[1] Other examples of scales homologous with stipules are the American Elm, Tulip-tree, Poplar and Magnolia. The leaves are plaited on the veins and covered with long, silky hairs. The venation is very distinct. The outer leaves are smaller and, on examining the branch, it will be seen that their internodes do not make so large a growth as the leaves in the centre of the bud.

[Footnote 1: See the stipules of the Pea, p. 31.]

The leaf-scars are small, soon becoming merely ridges running half round the stem.

The bud-rings are very plain and easily counted. For this reason, and because it branches freely, it is a good tree for measurements of growth, as is seen in the following tables. Nos. 1, 2, 3 and 4: were made by a class of girls, from fourteen to sixteen, from a tree on my lawn. No. 5 was made by a pupil, whom I taught by correspondence, from a tree of the same species in another town. No. 6 was made by myself from my own tree. The measurements of the first four tables were somewhat revised by me, as they were not perfectly accurate. The pupils should always be cautioned to measure from the beginning of one set of rings to the beginning of the next.[1]

[Footnote 1: Care must be taken to select branches well exposed to the light. Of course there are many circumstances that may aid or hinder the growth of any particular branch.]

NO. 1.

YEARS. GROWTH OF 1ST BRANCH. 2nd BRANCH. 3RD BRANCH 4TH BRANCH. MAIN AXIS. ———————————————————————————————— in. '79 8-1/2 — — — — '80 4-1/2 2 1-7/8 — — '81 3-1/2 1-1/8 2-5/8 — — '82 6 5/8 4-1/4 5-7/8 — '83 7-3/8 3-3/8 5-1/4 4 5-3/4 '84 2 1/2 3/4 3/8 5-3/8 '85 5/8 1/4 3/8 1/2 1 '86 5-5/8 7/8 4-3/8 3-1/8 5

NO. 2.

YEARS. GROWTH of 1ST 2nd 3RD 4TH 5TH MAIN AXIS. BRANCH BRANCH BRANCH BRANCH BRANCH ———————————————————————————————— in. '79 8 — — — — — — '80 3-1/2 5-1/4 5-1/2 5-5/8 — — — '81 4-3/4 3/4 1/2 2-1/2 2 — — '82 5-3/4 7/8 2 3/4 3/8 1/2 — '83 5-1/4 4-3/4 5-1/2 4 3-1/4 2-3/8 1-3/4 — '84 1/2 1 3/4 3/8 1 3/4 1 3/8 '85 2-3/4 1-3/4 4-3/8 3/4 3/4 2-1/8 3-1/4 1-1/4 '86 7-1/2 5-1/2 6-3/4 3 3 4-1/2 3-1/8 5

NO. 3.

YEARS. GROWTH of 1ST 2nd 3RD 4TH 5TH MAIN AXIS. BRANCH BRANCH BRANCH BRANCH BRANCH ——————————————————————————- in. '80 8-1/4 — — — — — '81 4-1/2 3-1/2 3-3/4 — — — '82 5-1/2 3/4 1-1/2 1 — — '83 3-1/4 3-3/4 4-1/2 3/4 2 1-1/4 '84 5-1/2 1/2 3/4 1 1/2 3 '85 1/2 1-3/4 1/2 3/8 1 1/2 '86 4-1/4 3-3/8 2-3/8 1-1/4 2-1/4 1-1/2

NO. 4.

YEARS GROWTH 1ST 2nd 3RD 4TH of MAIN BRANCH BRANCH BRANCH BRANCH AXIS ————————————————————- in. '81 7-3/4 — — — — '82 8-3/4 6 6 — — '83 6-3/4 5-1/4 4 4-3/4 5-1/2 '84 4-1/2 5/8 1-5/8 2-1/4 3-1/4 '85 2 5/8 3/16 2 3/4 '86 10-3/4 1-3/4 1/4 7-1/4 3-1/2

NO. 4. (cont.)

YEARS 5TH 6TH 7TH 8TH 9TH BRANCH BRANCH BRANCH BRANCH BRANCH —————————————————- in. '81 — — — — — '82 — — — — — '83 — — — — — '84 3/4 2-1/2 — — — '85 7/8 5/8 1/4 3/4 — '86 4-3/4 6-3/8 1 2-1/4 6-1/2

NO. 5.

YEARS GROWTH 1ST 2nd 3RD 4TH 5TH 6TH of MAIN BRANCH BRANCH BRANCH BRANCH BRANCH BRANCH AXIS ——————————————————————————- in. '82 6-7/8 —- —- —- —- —- —- '83 6-1/2 4-3/4 4-1/4 —- —- —- —- '84 4-3/4 1/4 1-3/4 3-1/2 —- —- —- '85 4-1/2 3/4 1 2-3/4 2-3/4 —- —- '86 6-1/4 2-1/4 4-3/4 6-3/4 2-3/4 5-3/4 —- '87 6-3/4 1-1/8 3-1/4 4 2-1/4 3 5-1/2

NO. 6.

YEARS MAIN 1ST 2ND 2ND 2ND 3RD 4TH AXIS BRANCH BRANCH BRANCH BRANCH BRANCH BRANCH ——————————————————————————- in. 1st 2nd side side '80 6-1/4 —- —- shoot. shoot. —- —- '81 8-3/4 6-3/4 —- —- —- —- —- '82 8-1/2 6-1/4 6-7/8 —- —- —- . '83 4-3/4 1-1/2 2-3/8 —- —- 4 . '84 3-1/2 3-1/8 5-1/8 —- —- 1-3/4 7/8 '85 4-1/2 3/8 4-3/4 2-1/4 —- 6 1 '86 6+ 6-3/4 12-1/8 5-1/2 10-1/2 8-7/8 5-1/8 '87 bough 2-1/2 8-3/4 4-1/4 4-1/4 4-6/8 3-3/4 broken.

One question brought up by these measurements is whether there is any correspondence in growth between the main axis and its branches. It appears in these tables that there is a general correspondence, in this tree at least. In the recitation of the class, whose tables are given above (Nos. 1, 2, 3 and 4), we took all the measurements of these four branches for the year 1885 and added them. We did the same for 1886, and compared the results. The total growth for 1885 was 31-15/16 inches; for 1886, leaving out the measurement of the twig whose entire growth was in that year, 109-3/4 inches or nearly 3-1/2 times as much. The proportion held in a general way throughout, there being only a single case of a branch where the growth was greater in the first year.[1] But there is a point that must not be overlooked in this connection. The branches of the Beech seem to grow about equally well in the first, second, third, or any succeeding year. In some trees, as the Ash, the axillary buds make a large growth, and the succeeding terminal buds carry on the branch much more slowly; in other trees, as the Cherry, a branch grows very slowly in the first few years and then suddenly takes a start. These facts would appear in tables of growth, made from branches of these trees, but the addition of results for any particular year would have no significance.

[Footnote 1: The spring of 1880 was a remarkably early one. Thus I find in my diary of that year the following entries:—

April 17. The red maples are in full bloom, the elms almost over. The leaves of the Horsechestnut are quite large. The lilacs are nearly in leaf. April 24. We went up to Waverley and found bloodroot up, spice bush out, violets, dog-tooths and anemones, also caltha. April 28. All the cherries are in full bloom. April 29. Picked an apple blossom in bud, beautifully pink.

The season was nearly three weeks earlier than usual. 1885 on the other hand was a late spring.]

In table No. 5, the addition of the measurements for 1885 and 1886 shows the growth in the latter year to be about twice that of the former. This branch came from a tree in another town. We have tried also to discover whether the number of leaves each year has any relation to growth. I cannot see that it has, but it requires many experiments to determine these points. To study this, make tables of the number of leaves on the branch each year. I think teachers would find it interesting to keep all data of this kind of work done by their classes, with a view to tabulation and comparison. The scholars themselves are exceedingly interested in anything that partakes of the nature of an original investigation.[1]

[Footnote 1: The class, previously mentioned, were much interested in the addition of their results. One of them asked me whether this subject of measurements had been treated in any book. I replied that I had never seen it mentioned. My attention was afterwards called to "What may be learned from a Tree," by Prof. Harlan Couitas. D. Appleton & Co., New York, 1863. I found, greatly to my surprise, that he had not only given diagrams of growth, but that he also had selected a Copper Beech as his example.]

The leaf-arrangement of the Beech is alternate, on the one-half plan. The small twigs turn upwards, so that all the spray is on the upper side, giving a flat appearance to the branch.[1] This gives the leaves a better exposure to the light. Both the terminal and axillary buds grow freely, thus forming long, straight limbs, with many branches and much fine spray.

[Footnote 1: Phyllotaxy is treated later, by a comparison and study of many branches, but the teacher can draw the pupils' attention to the fact that each Beech leaf and twig is on exactly the opposite side of the branch from the preceding one. This allows all the twigs to grow towards one side of the branch, whereas in trees on the two-fifths plan, as the Apple, Poplar, Oak, etc., no such regularity would be possible, on account of their many different angles with the stem.]

The bark of the Beech is beautifully smooth. The extreme straightness of the trunk and limbs is very striking, and may be compared to the crooked limbs of the Horsechestnut, where the branch is continually interrupted by the flower-cluster. In the Beech the flowers are axillary.


How are the scales of the Beech bud arranged?

How many leaves are there in the bud?

How does the arrangement of the scales and leaves in the bud differ from that of the Horsechestnut?

How are the leaves folded in the bud?

What is the arrangement of the leaves on the stem?

How does this differ from Horsechestnut and Lilac?

How old is your branch?

How old is each twig?

What years were the best for growth?

How does the growth of the branches differ from that of Horsechestnut? From Lilac?

Explain these differences with reference to the growth and arrangement of the buds?

In what direction do the twigs grow?

How does this affect the appearance of the tree?

Compare the amount of spray of the Beech and Horsechestnut and explain the reason of the difference.

These questions are only intended for review, they are never to be used for the first study of the specimen.

AMERICAN ELM (Ulmus Americana).

The buds are covered with brown scales, which are hairy on the edges. The flower-buds are larger than the leaf-buds and are in the axils of the lower leaves of the preceding year. Each leaf in the bud is enclosed by a pair of scales. They are so small that the pupils, unused to delicate work, will hardly discover them. Under a glass they can be seen to be ovate, folded on the midrib with the inner face within (conduplicate), and with an ovate scale joined to the base of the leaf on either side. The scales thus show themselves to be modified stipules. The venation of the leaves is very plain. The scales are much larger than the leaves. The flower-buds contain a cluster of flowers, on slender green pedicels. The calyx is bell-shaped, unequal, and lobed. The stamens and pistil can be seen. The flower-clusters do not seem to leave any mark which is distinguishable from the leaf-scar.

The leaf-scars are small and extend about half around the stem. The arrangement is alternate on the one-half plan. There are three dots on the scar.

The rings are quite plain. The tree can be used to make tables of growth, like those of the Beech.

The buds will probably be too small for examination by the pupils, at present, but their position and development can be studied, and are very instructive. As the leaf-buds are all on the ends of the branchlets, the twigs and branches will be just below the bud-rings, and then there will be a space where no twigs nor branches will be found, till the next set of rings is reached. This gives the branches more room to develop symmetrically. The terminal buds do not develop in the Elm, in old trees, the bud axillary to the last leaf of the season taking its place, and most of the other axillary buds growing also. This makes the tree break out into very fine spray. A tree like the Elm, where the trunk becomes lost in the branches, is called deliquescent; when the trunk is continued to the top of the tree, as in the Spruce, it is excurrent.

The small, feathery twigs and branches that are often seen on the trunks and great limbs of the elm grow from buds which are produced anywhere on the surface of the wood. Such buds are called adventitious buds. They often spring from a tree when it is wounded.

"The American elm is, in most parts of the state, the most magnificent tree to be seen. From a root, which, in old trees, spreads much above the surface of the ground, the trunk rises to a considerable height in a single stem. Here it usually divides into two or three principal branches, which go off by a gradual and easy curve. Theses stretch upwards and outwards with an airy sweep, become horizontal, the extreme half of the limb, pendent, forming a light and regular arch. This graceful curvature, and absence of all abruptness, in the primary limbs and forks, and all the subsequent divisions, are entirely characteristic of the tree, and enable an observer to distinguish it in the winter and even by night, when standing in relief against the sky, as far as it can be distinctly seen."[1]

[Footnote 1: A Report on the Trees and Shrubs growing naturally in the Forests of Massachusetts. By Geo. B. Emerson, Boston, Little, Brown and Co., 1875.

This book will be found very useful, containing careful descriptions of many trees and shrubs, and interesting facts about them.]


How do the flower-buds differ from the leaf-buds in position and appearance?

What is the arrangement of the leaves?

What other tree that you have studied has this arrangement?

How old is your branch?

Where would you look to see if the flower-cluster had left any mark?

Why is it that several twigs grow near each other, and that then comes a space without any branches?

What buds develop most frequently?

How does this affect the appearance of the tree?

What is a tree called when the trunk is lost in the branches?

BALM OF GILEAD (Populus balsamifera, var. candicans).

The buds are pointed: the terminal slightly angled, the axillary flattened against the stem.[1] Some of the axillary buds contain leaves and some flowers; the appearance of the leaf-buds and flower-buds being the same. The scales of the bud are modified stipules. The terminal buds have about three pairs of the outer scales brown and leathery. The inner scales, as well as the leaves, are coated with resinous matter, which has a strong odor and a nauseous taste. The smaller outer scales have no corresponding leaf, and apparently are modified stipules of the leaves of the preceding year, but the larger ones have a leaf to each pair of scales. The outer and inner leaves are small, the middle ones larger. Comparing the branch, it will be seen that these leaves make the largest growth of internode. The leaves are rolled towards the midrib on the upper face (involute). There are about ten which are easily seen and counted, the inner ones being very small, with minute scales. The axillary buds have a short thick scale on the outer part of the bud, then about three pairs of large scales, each succeeding one enwrapping those within, the outer one brown and leathery. The scales of the flower-buds are somewhat gummy, but not nearly so much so as those of the leaf-buds. Within is the catkin. Each pistil, or stamen (they are on separate trees, dioecious) is in a little cup and covered by a scale, which is cut and fringed.

[Footnote 1: These buds cannot be satisfactorily examined in cross section, on account of the resin. The scales must be removed one by one, with a knife, with a complete disregard of the effect upon the hands.]

The leaf-scars are somewhat three-lobed on the young parts, with three dots, indicating the fibro-vascular bundles, which ran up into the leaf. The scars are swollen, making the young branches exceedingly rough. In the older parts the scars become less noticeable. Strong young shoots, especially those which come up from the root, are strongly angled, with three ridges running up into each leaf-scar, making them almost club-shaped. There are often from twenty to thirty leaves in one year's growth, in such shoots, and all the leaves are not rudimentary in the bud. The growth in this case is said to be indefinite. Usually in trees with scaly buds the plan of the whole year's growth is laid down in the bud, and the term definite is applied. Branches, like the Rose, that go on growing all summer grow indefinitely.

The bud-scale scar is quite different from the other trees which we have examined. It is not composed of definite rings, but of leaf-scars with long ridges running from each side of them, showing the scales to be modified stipules. The leaf-scars have become somewhat separated by the growth of the internodes. In the Beech, there are eight, or more, pairs of scales with no leaves, so that the internodes do not develop, and a ring is left on the branch.

The flower-cluster leaves a concave, semicircular scar, in the leaf-axil.

The terminal buds are the strongest and not very many axillary buds develop, so that the tree has not fine spray.

The leaf-arrangement is alternate, on the 2/5 plan. Phyllotaxy is not yet to be taken up, but the pupils should be shown the different angles of the branching of the twigs, and told to compare them with Beech and Elm.


In which buds are the flower-clusters?

Are there flowers and leaves in the same buds?

What are the scales of the bud?

How are the leaves folded in the bud?

How do the axillary and terminal buds differ?

What are the dots on the leaf-scars?

Why is there no distinct band of rings as in Beech?

How old is your branch?

Where do you look for flower-cluster scars?

Which buds are the strongest?

How does this affect the appearance of the tree?

What makes the ends of the branches so rough?

Compare the arrangement of the twigs and branches with Beech and Elm, with Horsechestnut and Lilac.

TULIP-TREE (Liriodendron Tulipifera).

The buds are small, flat, and rounded at the apex. They are sheathed by scales, each leaf being covered by a pair, whose edges cohere. The outer pair are brown and are the stipules of the last leaf of the preceding year. The leaves are conduplicate, as in Magnolia, and have the blade bent inwards on the petiole (inflexed). Their shape is very clearly to be seen, and no bud is more interesting in the closeness of its packing. Axillary buds are often found within. The flowers grow high upon the trees and towards the ends of the branches.

The leaf-scars are round with many dots. The scar of the stipules is a continuous line around the stem, as in Magnolia.

CHERRY (Prunus Cerasus).

The leaf-buds are terminal, or in the axils of the upper leaves of the preceding year; the flower buds are axillary. There is but one bud in each axil, and usually two or three flowers in each bud, but the leaves on the twigs are crowded and the flowers therefore appear in clusters. The blossom-buds are larger and more rounded than the leaf-buds.

The buds of the tree develop very easily in the house, and as they are so small they can be better studied in watching them come out, than by attempting to dissect them, unless the scholars are sufficiently advanced to use the microscope easily. It is always bad for a pupil to attempt to describe what he sees but imperfectly. He will be sure to jump at any conclusions which he thinks ought to be correct.

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