ui I 1761 fe) 2 O cx e) uw fe) > 7) wi 2 r-4 I 3 ipa (NIV.OF 7) (ORONTO ' UBRARY ee. Se ee ae — + LIBRARY FACULTY OF FORESTRY UNIVERSITY OF TORONTO . yu ie \ ‘ # ; : : ‘ 3 . eh \ 4 A , Ae) e CL Aee Py , ‘ 7 ma Sa iy f t . ms i set 2 ae ‘ wie ck y ‘s en FOP ’ “ ye ¢ sae ity Ld eS ( ; DA TUE CW aT Wipes yay | : P ry ‘ | ik ay —* «i olin’ -~ ~: j . al ; ay . ; ». ¥ f if 1 ai . re 4 7 7 ‘ TAS wi 4 . AS ee Digitized by the Internet Archive in 2007 with funding from Microsoft Corporation http://www.archive.org/details/botanyelementaryOObailuoft BO tay 1. “From fragile mushrooms, delicate water-weeds and pond-scums, to floating leaves, soft grasses, course weeds, tall bushes, slender climbers, gigantic trees, and hanging moss.” See Chapter I. B BOTANY aoe M BN TA EY Oe Xx 7 SEIS (eee OM s KOON Tyo) BY mt BATLEY % L 0 «Pe / | {| j2Qew Work THE MACMILLAN COMPANY LONDON: MACMILLAN & CO., Lp. 1900 CopyriGHT, 1900 By L. H. BAILEY Mount jOleasant JPrinterp J. Horace McFarland Company Harrisburg, Pa. PARAGRAPHS FOR THE TEACHER THis book is made for the pupil: “Lessons with Plants” was made to supplement the work of the teacher. There are four general subjects in this book: the nature of the plant itself; the relation of the plant to its surroundings; histological studies; determination of the kinds of plants. From the pedagogical point of view, the third is the least important. Each of the subjects is practically distinct, so that the teacher may begin where he will. The schools and the teachers are not ready for the text-book which presents the subject from the view- point of botanical science. Perhaps it is better that the secondary schools attempt only to teach plants. A book may be ideal from the specialist’s point of view, and yet be of little use to the pupil and the school, i: fe, Se ae The pupil should come to the study of plants and animals with little more than his natural and native powers. Study with the compound microscope is a specialization to be made when the pupil has had experience, and when his judgment and sense of relationships are trained, (v) vl PARAGRAPHS FOR THE TEACHER One of the first things that a child should learn when he comes to the study of natural history is the fact that no two things are alike. This leads to an apprehension of the correlated fact that every animal and plant contends for an opportunity to live, and this is the central fact in the study of living things. The world has a new meaning when this fact is under- stood. The ninety and nine cannot and should not be botanists, but everyone can love plants and nature. Every person is interested in the evident things, few in the abstruse and reecondite. Education should train persons to live, rather than to be scientists. Now and then a pupil develops a love of science for science’s sake. He would be an investigator. He would add to the sum of human knowledge. He should be encouraged. There are colleges and universities in which he may continue his studies. In the secondary schools botany should be taught for the purpose of bringing the pupil closer to the things with which he lives, of widening his horizon, of intensifying his hold on life. It should begin with familiar plant forms and phenomena. It should be related to the experiences of the daily life. It should not be taught for the purpose of making the pupil a specialist: that effort should be retained for the few who develop a taste for special knowledge. It is often said that the high-school pupil should begin the study of botany with the lowest and simplest forms of a PARAGRAPHS FOR THE TEACHER vill life. This is wrong. The microscope is not an intro- duction to nature. It is said that the physiology of plants ean be best understood by beginning with the lower forms. This may be true: but technical plant physiology is not a subject for the beginner. Other subjects are more important. The youth is by nature a generalist. He should not be forced to be a_ specialist. A great difficulty in the teaching of botany is to determine what are the most profitable topies for con- sideration. The trouble with much of the teaching is that it attempts to go too far, and the subjects have no vital connection with the pupil’s life. Good botanical teaching for the young is_ replete with human interest. It is connected with the common associations. The teacher often hesitates to teach botany because of lack of technical knowledge of the subject. This is well; but technical knowledge of the subject does not make a good teacher. Expert specialists are so likely to go into mere details and to pursue particu- lar subjects so far, when teaching beginners, as_ to miss the leading and emphatic points. They are so cognizant of exceptions to every rule that they qualify their statements until the statements have no force. There are other ideals than those of mere accuracy. In other words, it is more important that the teacher be vili PARAGRAPHS FOR THE TEACHER a good teacher than a good botanist. One may be so exact that his words mean nothing. But being a good botanist does not spoil a good teacher. An imperfect method that is adapted to one’s use is better than a perfect one that cannot be used. Some school laboratories are so perfect that they dis- courage the pupil in taking up investigations when thrown on his own resources. Imperfect equipment often encourages ingenuity and originality. A good teacher is better than all the laboratories and apparatus. Good teaching devolves on the personality and enthusiasm of the teacher; but subject-matter is a prime requisite. The teacher should know more than he attempts to teach. Every teacher should have access to the current botanical books. The school library should contain these books. By consulting the new books the teacher keeps abreast of the latest opinion. When beginning to teach plants, think more of the pupil than of botany. The pupil’s mind and sym- pathies are to be expanded: the science of botany is not to be extended. The teacher who thinks first of his subject teaches science; he who thinks first of his pupil teaches nature-study. Teach first the things nearest to hand. When the pupil has seen the common, he may be introduced to the rare and distant. We live in the midst of common things. PARAGRAPHS FOR THE TEACHER 1X The old way of teaching botany was to teach the forms and the names of plants. It is now proposed that only function be taught. But one cannot study function intelligently without some knowledge of plant forms and names. He must know the language of the subject. The study of form and function should go together. Correlate what a plant is with what it does. What is this part? What is its office, or how did it come to be? It were a pity to teach phyllotaxy with- out teaching light-relation: it were an equal pity to teach light-relation without teaching phyllotaxy. Four epochs can be traced in the teaching of elementary botany: (1) The effort to know the names of plants and to classify. This was the outgrowth of the earlier aspect of plant knowledge, when it was necessary to make an inventory of the things in the world. (2) The desire to know the formal names of the parts of plants. This was an outgrowth of the study of gross morphology. Botanies came to be dic- tionaries of technical terms. (3) The effort to develop the powers of independent investigation. This was largely a result of the German laboratory system, which developed the trained specialist investigator. — It emphasized the value of the compound microscope and other apparatus. This method is of the greatest service to botanical science, but its introduction into the secondary schools is usually unfortunate. (4) The effort to know the plant as a complete organism living its own life in a natural way. In the begin- ning of this epoch we are now living. PARAGRAPHS FOR THE TEACHER A There is a general protest against the teaching of ‘bie names” to pupils; but the pupil does not object to technical terms if he acquires them when he learns the thing to which they belong, as he acquires other language. When a part is_ discovered the name becomes a necessity, and is not easily forgotten. He should be taught not to memorize the names. The “hard” words of to-day are the familiar words of to-morrow. There are no words in this book harder than ehrysanthemum, thermometer, and hippopotamus. The book should be a guide to the plant: the plant should not be a guide to the book. Plants should not be personified or endowed out- right with motives; but figures of speech and_ para- bles may often be employed to teach a lesson or to drive home a_ point. Excite the pupil’s interest rather than his wonder. The better the teacher, the less will he confine him- self to the questions at the end of the lesson. Botany always should be taught by the “laboratory method:” that is, the pupil should work out the sub- jects directly from the specimens themselves. Specimens mean more to the pupil when he collects them. No matter how commonplace the subject, a speci- men will vivify it and fix it in the pupil’s mind. A living, growing plant is worth a score of herba- rium specimens. PARAGRAPHS FOR THE TEACHER X1 Acknowledgements. —To hundreds of young people in many places the author is under the profoundest obligations, for they have instructed him in the point of view. Specific aid has been given by many persons. From the teacher’s point of view, proofs have been read by Miss Julia E. Rogers, Minburn, Iowa; Miss L. B. Sage, Norwich, N. Y.; Mrs. Mary Rogers Miller, lecturer of the Bureau of Nature-Study in Cornell University. From the botanist’s point of view, all the proofs have been read by Dr. Erwin F. Smith, of the Division of Vegetable Physiology and Pathology, United States Department of Agriculture, and his suggestions have been invaluable. Chapters XI and XII are adapted from two papers which were con- tributed to a Farmer’s Reading-Course under the author’s charge, by Dr. B. M. Duggar, of Cornell University. Two specialists, with whom it has been the author’s privilege to associate as teacher and collaborator, have contributed particular parts: Dr. K. C. Davis, the greater portion of Part III, and H. Hasselbring, the most of Chapter XXV. On special problems the author has had the advice of Dr. kK. M. Wiegand, of Cornell University. Preah BAILEY. HORTICULTURAL DEPARTMENT, CORNELL UNIVERSITY, ITHACA, N. Y. October 1, 1900, The common pitcher plant, Sarracenia purpurea. The pitchers, or leaves, hold water, in which organic matter collects. This decaying matter probably aids somewhat in nourishing the plant. CONTENTS PART I THE PLANT ITSELF CHAPTER evil, XVII. XVIII. XIX. XX. XXI. XXII. The Plant as a Whole . The Root . The Stem . eet hE nares Propagation by Means of Roots and Stems . How the Horticulturist Propagates Plants by Means of Roots and Stems . Food Reservoirs . . Winter Buds . Plants and Sunlight . Struggle for Existence amongst the Branches . . The Forms of Plants How the Plant Takes inthe Soil Water . The Making of the Living Matter Dependent Plants . Leaves and Foliage Morphology, or the Study of the Forms of Members How Plants Climb Flower-Branches The Parts of the Flower . Fertilization and Pollination Particular Forms of Flowers Fruits Dispersal of Seeds (xiii) Plant PAGE X1V CONTENTS CHAPTER PAGE XI Genminaionee neat se a en a oe ee LG XXIV. Phenogams and Cryptogams . 7 RXV. Studies: in Cryptocams pe see) ee cae ee PONT JO THE PLANT IN Its ENVIRONMENT XOX Vl. “Wihere: elantsiGuows. oases Sec = ee ee pan era XXVII. Contention with Physical Environment. ...... 203 MEX VIL. Competition with Mellowsy meee wae feast MONIES, IPI TA SOCIEMES 3 56 2 5 4 o . ect Se aa ae ah VOOM, Weneieymorm anal Ihe 1veRiUnS) 4.6 8 = a 2 6 6 5 a 6 a o 7 Bes PAR in HIsToLoGy, OR THE MINUTE STRUCTURE OF PLANTS XOX. Whe Cell. = Saeeesa BD A ne ee noe, ee OO Roo. Contents aud Products om Cellsm . 0 sc) eer ORO UY SSUES eee ree BAe re eR mee ree gente NG) NOOO. Structure Of Stems andy hOOtses elem cen cn t-un nnn OO, NeNOve Structuresof eaves! = on a eee nee ee ee) PART IV THE KINDS oF PLANTS (p. 275) BOTANY PART I—THE PLANT ITSELF CHAPTER I THE PLANT AS A WHOLE 1. Aplant is a living, growing thing. It partakes of the soil and air and sunshine. It propagates its kind and covers the face of the earth. It has much with which to contend. It makes the most of every opportunity. We shall learn its parts, how it lives, and how it behaves. 2. THE PARTS OF A PLANT. — Our familiar plants are made up of several distinct parts. The most prominent of Soar these parts are root, stem, leaf, flower, -« %y fruit and seed. Fig.2. Familiar plants differ wonderfully in size and shape,— from fragile mushrooms, delicate water- weeds and pond-scums, to floating leaves, soft grasses, coarse weeds, tall bushes, slender climbers, gigantic trees, and hanging moss. See frontispiece. 3. THE STEM PART.—In most plants there is a main central part or shaft on . 2. A buttercup plant, which the other or secondary parts are snowing the various parts. A (1) 2 THE PLANT AS A WHOLE borne. This main part is the plant axis. Above ground, in familiar plants, the axis bears the branches, leaves and flowers; below ground, it bears the roots. 4. The rigid part of the plant, which persists over win- ter and which is left after leaves and flowers are fallen, is the framework of the plant. The framework is composed of both root and stem. When the plant is dead, the framework remains for a time, but it slowly decays. The dry winter stems of weeds are the framework or skeleton of the plant. Figs. 3 and 4. The framework of trees is the most conspicuous part of the plant. 5. THE ROOT PART.—The root bears the stem at its apex, but otherwise it normally bears only root-branches. The stem, however, bears leaves, flowers and fruits. Those living surfaces of the plant which are most exposed to light are green or highly colored. The root tends to grow downward, but the stem tends to grow upward toward light and air. The plant is anchored or fixed in the soil by the roots. Plants have been called “earth parasites.” 6. THE FOLIAGE PART.— The leaves precede the flowers in point of time or in the life of the plant. The flowers always precede the fruits and seeds. Many plants die when the seeds have matured. The whole mass of leaves of any plant or any branch is known as its foliage. 7. THE PLANT GENERATION.— The course of a plant’s life, with all the events through which the plant naturally passes, is known as the plant’s life-history. The life- history embraces various stages or epochs, as dormant seed, germination, growth, flowering, fruiting. Some plants run their course in a few weeks or months, and some live for centuries. 8. The entire life-period of a plant is called a genera- tion. It is the whole period from birth to normal death, without reference to the various stages or events through which it passes. THE PLANT GENERATION 3 9. A generation begins with the young seed, not with germination. Jt ends with death — that is, when no life is left in any part of the plant, and only the seed or spore remains to perpetuate the kind. In a bulbous plant, as a lily or an onion, the generation does not end until the bulb dies, even though the top is dead. 10. When the generation is of only one season’s duration, the plant is said to be annual. When it is of two seasons, it is biennial. Biennials usually bloom the second year. When of three or more seasons, the plant is perennial. Examples of annuals are pigweed, bean, pea, garden sunflower; of biennials, fox- glove, mullein, teasel, parsnip, carrot; of perennials, dock, meadow grass, cat-tail, and all shrubs and trees. 11. DURATION OF THE PLANT BODY.— Plant strue- tures which are more or less soft and which die at the close of the season are said to be herbaceous, in contra- distinction to being ligneous or woody. A plant which is herbaceous to the ground is called an herb; but an herb may have a woody or perennial root, in which case it is called an herbaceous perennial. Annual plants are classed as herbs. Examples of herbaceous perennials are butter- | , Ve Vite (A. te) Ww Se 3. Plant of a wild 4. Framework sunflower, of No. 3. cup (Fig. 2), bleeding heart, violet, water-lily, many grasses, dock, dandelion, golden rod, asparagus, rhubarb, many wild sunflowers (Figs. 3, 4). 12. Many herbaceous perennials have short generations. + THE PLANT AS A WHOLE They become weak with one or two seasons of flowering and gradually die out. Thus red clover begins to fail after the second year. Gardeners know that the best bloom of hollyhock, larkspur, pink, and many other plants, is secured when the plants are only two or three years old. 13. Herbaceous perennials which die away each season to bulbs or tubers, are sometimes called pseud-annuals (that is, false annuals). Of such are lily, crocus, onion, potato. i sayy Se 272° |- Peo a7 ok Bes este uf Cone Tce oa 5. A shrub or bush. Dogwood osier. 14. Plants which are normally perennial may become annual in a shorter-season climate by being killed by frost, rather than by dying naturally at the end of a season of growth. Such plants are called plur-annuals in the short- season region. Many tropical perennials are plur-annuals when grown in the north, but they are treated as true an- nuals because they ripen sufficient of their crop the same season in which the seeds are sown to make them worth cultivating, as tomato, red pepper, castor bean. HOW PLANTS ARE MODIFIED 5 15. Woody or ligneous plants are usually longer lived than herbs. Those which remain low and produce several or many similar shoots from the base are called shrubs, as lilac, rose, elder, osier. Fig.5. Low and thick shrubs are bushes. Plants which produce one main trunk and a more or less elevated head are trees. Fig. 6. 16. PLANTS ARE MODIFIED BY THE CONDITIONS IN WHICH THEY GROW.—In most plants, the size, form and general appearance vary or change with the conditions in which the plant grows. That is, there is no uniform or necessary form into which plants shall grow. No two plants are exactly alike. Observe plants of the same kind and age, and see how they differ or vary. The farmer and gar- dener can cause plants to be large or small of their kind, by chang- ing the conditions or circumstan- ces under which they grow. ‘ 17. No two parts of the same EEG af Kee & the. Leas 4, SOOT ARES ings Re hos . ; ie some plants, several leaves occur at one level, 79. Rhubarb grown in the light. being arranged in a circle around the stem. Such leaves are said to be ver- ticillate or whorled. Leaves arranged in this way are usually narrow. 113. Although a definite arrangement of leaves is the rule in most plants, it is subject to modification. On shoots which receive the light only from one side or which grow in difficult positions, the arrangement may not be definite. Examine shoots which grow on the under side of dense tree-tops or in other partially lighted positions. D 50 PLANTS AND SUNLIGHT 114. The direction or “hang” of the leaf is usually fixed, but there are some leaves which change their direction between daylight and darkness. Thus, leaves of clover (Fig. 82), bean, locust, and many related plants, “sleep” at night; also oxalis. It is not asleep inthe sense in which animals sleep, however; but its function is not well understood. 115. Leaves usually expose one — x80. Ali the leaves are exposed particular surface to the light. fp ent This is because their internal structure is such that light is most efficient when it strikes this surface, as we shall learn later on. Some plants, however, expose both surfaces to the light, and their leaves stand vertical. Others endeavor to avoid the intense light of mid- day and to turn in the direction of least light. Leaves standing edgewise are said to exhibit polar- ity. They are “compass plants” if they point north and south. The famous compass plant or silphium | eee. of the prairies and the Ba aerate & wild lettuce are examples A of plants having polar 81. Phyllotaxy of box-elder, elm, apple. leaves. (Wild lettuce [Lactuea Seariola] isa common plant on roadsides; p. 356.) Every leaf has a story to tell of the value of sunlight. THE WINTER BUDS SHOW EFFECT OF SUNLIGHT 51 116. WINTER BUDS SHOW WHAT HAS BEEN THE EFFECT OF SUNLIGHT.—Buds are borne in the axils of the leaves (86), and the size or vigor of the leaf determines to a large extent the size of the bud. a Notice that, in most instances, the largest buds are nearest the tip (Fig. 83). If the largest ones are not near the tip, there is some special reason for it. Examine the shoots on trees 82. Day and night positions of and bushes. the clover leaf. 117. The largest buds usu- ally start first in spring, and the branches which arise from them have the advantage in the struggle for exis- tence. Plants tend to grow most vigorously from their ends. Observe that only the terminal 4 bud grew in the hickory twig in Fig. @ 60. Every bud has a story to tell of the value of sunlight. REvIEw.— What is the relation of the plant to sunlight ? Does its form ever depend on its relation to light? In what direction do the tops of plants grow? Where are the most vigorous branches? What is heliotropism! Why are trees sometimes unsymmetrical? Do you know any instances yourself? What is one way in which plants profit by the climbing habit? Is there struggle amongst branches? Explain. Where are leaves borne in reference to light? Where are leaves usually largest? Do they develop in darkness? Are leaves borne di- rectly above one another? How may leaves 83. The big terminal buds.—Hickory, be arranged? Explain what phyllotaxy is. Are leaves always arranged definitely? Explain the arrangement in some plant which is not mentioned in this lesson. What is the “sleep” of leaves? Which surface of the leaf is ex- posed? What are compass plants? How do buds show what the effect of sunlight has been? What buds start first in spring? CHAPTER IX STRUGGLE FOR EXISTENCE AMONGST THE BRANCHES 118. NO TWO BRANCHES ARE ALIKE.— Hvery twig has a history. It has to contend for air and sunlight, and a place in which to grow. Its size and shape, therefore, depend on the conditions under which it lives. Observe the long, straight, big-leaved shoots on the top of the plant, and the short, weak, crooked ones on the inside or under side. 119. There is struggle for existence for every twig and every leaf. Those finding the best conditions live and ee ae ee 84. The struggle for life.—Mulberry shoot. thrive; those finding the poorest die. The weak are overpowered and finally perish: this prunes the tree, and tends to make the strong the stronger. Observe the competition in the branch photographed in Fig. 84. Pick out the dead twigs, the weak ones, the strong ones. 120. THE BUDS MAY NOT GROW.— There is not room in a tree-top for all the buds to grow into branches. Some buds (52) THE BUDS MAY are suppressed. Branches die. So it comes that branches are not arranged regularly, although the buds may be. In the Tar- tarlan “tree” honey- suckle the buds are oppo- Fig. 85 shows how or site ; the branches are. 121. The results of the struggle for existence in the be expressed Consider that tree-top can in figures. every bud is the germ or starting point of a branch. any Willow. 86. Scars of the dormant buds bears. of the number of branches: if New! NOT GROW CQ erooked 85. The branching is and irregular, Ob- serve at what distances apart the buds are usually borne on plant, number of buds which the plant “ and estimate the has borne: count the number of branches which the tree actually It will be found that the number of buds is far in excess the difference between the numbers shows how many buds or branches have failed. Or, count the buds on any branch, and figure up the possibilities, A branch 12 inches lone, for instance, has 10 buds. If eaeh bud erows, at the end of the next season there 54 STRUGGLE AMONGST BRANCHES will be 10 branches, each of which may have 10 buds. At the end of the second year there will be 100 branches ; at the end of the third, 1,000. Can 1,000 branches be borne on a 4-year-old branch 12 inches long? Or, count the old bud-sears on the branches — for the places of the buds persist as wrinkles in the bark, often for many years (Fig. 86). One ean often locate these bud-sears on old branches with his eyes closed by running his fingers over the bark. 122. Buds which fail to grow are ealled dormant buds. They are usually the weakest ones,—those which grew im the most uncongenial conditions. They are to- wards the base of the shoot. We have seen (117) that it is the terminal or uppermost buds which are most likely to grow. The dormant buds gradually die. They may live four or five years on some plants. If the other buds or branches fail or are injured, they may grow, but usu- ally they die. 123. Dormant buds must not be confounded with ad- ventitious buds. We have learned (54) that adventitious buds are those which are formed at unusual times or places, because of some disturbance of the part. If a large branch is cut off, suckers or watersprouts are thrown out near the wound: these arise from buds which are made for the occa- sion. These buds did not exist there. In many countries it is a custom to “pollard” or eut off the tops of trees every few years for the firewood; and strong adven- titious shoots arise along the trunk. Fig. 87. 124. WHERE THE BRANCHES GROW.— Because new shoots tend to arise from the top of the twigs, the branches of most trees are in tiers or layers. These tiers often can be traced in trees 50 and 100 years old. Try it in any oak, maple, ash, or other tree. For practice, begin with young, vigorous trees (Figs. 88 and 89). 125. When part of a top is removed, the remaining pollard willow A mun hus added to the struggle for existence Italy In this case, 56 STRUGGLE AMONGST BRANCHES branches fill the space. The branches are attracted by the light and air, and grow in that direction. A pruned or injured top always tends to come back to equi- librium. 126. A mangled or broken plant tends to regain its former posi- tion. From fallen trees, upright shoots arise. In Fig. 90 observe the new trunk arising from the center of the arch; see that the main trunk is smaller beyond that point. REVIEW.— What is meant 88. Tiers of 89. Even in old trees branches on the tiers can be by the statement that every young tree. traced. twig has a history? Upon what does the shape and size of a branch depend? Explain what you mean by the struggle for existence. Why do not all buds grow? If buds are arranged in mathematical order, why are not branches? How may the effect of struggle for existence be expressed in figures? Select some braneh and explain. Define dormant buds. Adyvyentitious buds. Why are branches in tiers, or borne at intervals? How do plants tend to re- gain their form and posi- tion, when injured ? Notre.—Let the pupil work out the history of some branch. It is better to select a branch which is vigorous. He should first determine, if the shoot is dormant, how much grew the previous season. The last year’s growth bears buds on the 90. The erect bole on the fallen trunk. ‘SS in — we 714° ~~ a uw ; > o ’ 05, October 18th, 58 STRUGGLE AMONGST BRANCHES main axis, not on side branches ; and the“ ring” (sears of bud-seales) marks the junction between the different years’ growth. Notice this ring in Fig. 83. The teacher will find many twigs worked out in “ Les- sons with Plants.” Figs. 91-95 show an actual case. These drawings were all made with the greatest care from one elm twig. The twig (Fig. 91) shows three years’ growths. The side branch is evidently only one year old, for it did not arise until the twig which bears it was one year old. Note that only one of the buds made a branch. There are five blossom buds. Fig. 92 shows the twig in bloom. Fig. 93 shows it in fruit and leaf. Fig. 95 shows the net result. The side branch grew from a to s and made two blossom buds. The tip of the main shoot (Fig. 91) was broken in a storm. The two buds next in succession grew. Each made flower buds. Observe how many buds on this elm shoot have failed. Crushed by storm, the tree still shoots upward. CHAPTER X THE FORMS OF PLANTS 127. Although the form of the branch, and to some extent the entire plant, is determined by a struggle with the conditions in which it grows, nevertheless each hind of plant has its own peculiar habit of growth. The lum- 96. Different forms of trees. berman distinguishes the kinds of trees by their “looks,” rather than by their leaves or flowers, as the botanist does. The farmer usually does the same with his culti- vated plants. 128. The habit of a plant is determined by its size, general style or direction of growth, form of head, and method of branching. The general style or stature of plants has been mentioned in Chapter III[—they may be erect, strict, creeping, decumbent, and the like. The shape of the top or head is well illustrated in trees. Note the general effect of the mass, as seen at a distance. The elm is vase-form or round-headed (Fig. 96, which is cited again to teach another lesson, p.223). So (59) = 97. Round-headed and fastigiate trees, 60 THE FORMS OF PLANTS are maple, beech, and apple trees. The Lombardy poplar (Fig. 97) is columnar or fastigiate. Young spruces and firs are conical. Heads may be narrow, wide, flat, symmetrical, irreg- ular or broken. 129. The general leaf- age or furnishing of the top is different for each kind. The top may be dense or thin. The foli- age may be heavy, light, large, small. Compare maples and elms, apples and peaches, and other trees. 130. The trunk or bole of the tree is one of its most conspicuous 98. The unbranched trunks of palms. features. Observe the strict straight trunk of the palm (Fig. 98), and the fork- ing trunks of elms and maples. Observe that no two trees have trunks which are quite alike. The bark is different for each kind of plant. 131. Plants awaken certain thoughts or feel- ings: they are said to have expression. This expression is the source of much of our pleasure . 99. f in wi .—Russiz istle. in them i Trees are The plant form in winter.—Russian thistle particularly expressive. One suggests restfulness, because of its deep shady top; another gaiety, from its moving, EXPRESSIONS OF PLANTS 61 small, light-colored leaves; another heaviness, from its very large, dull foliage; another strength, from the massive branches; another grace, from the flowing outline or flexile growth. We think of the oak as strong, the willow as lithe, the aspen as weak, and the like. Irregular or 100. The many trunks of an old olive tree. Italy. gnarly trees suggest struggle. Jf all plants, or even all trees, were alike, we should have little pleasure in them. 132. The expression of a plant depends to some extent on the character of the shadows in the top. These shadows (or lights and shades) are best seen by looking at the plant when the sun is low and behind the observer. 62 THE FORMS OF PLANTS Stand at some distance. Look at the dark places in the old pasture maple: they are lumpy and irregular. In the pasture beech they are in layers or strata. The shadows depend mostly on the method of branching. Those who take photographs know how the “high lights” and shadows develop on the plate. 133. The habit of a plant is usually most apparent 101. A pear tree of the Kieffer variety. 102. A pear tree of the Hardy variety. when it is leafless. The framework is then revealed. Woody plants are as interesting in winter as in summer. Observe their forms as outlined against the sky—every one different from every other. Notice the plant forms as they stand in the snow. Fig. 99. How do stems of the pigweed differ from those of burdock and grasses? Observe how the different plants hold snow and ice. 134. The more unusual the shape of any tree or other INTEREST IN PLANT FORMS 63 plant, the greater is our interest in it, because our curiosity is awakened. Some unusual circumstance or condition has produced the abnormal form. Such plants should be pre- served whenever possible. Fig. 100. REVIEW.— What do you mean by the statement that each kind of plant has its own habit (36)? How do plants differ in habit? Name some of the forms of tree-tops. How may plants differ in the furnish- ing of the top? Is the trunk characteristic? Bark? Bring in and describe the bark of three kinds of trees. What is the expression of a tree? What are some of the expressions? Explain what you under- stand by the shadows in the top. On what do the shadows chiefly depend? What is there to see in plants in winter? Why are we interested in plants of unusual form? Tell how any two trees differ in “looks.” Nore.—One of the first things the pupil should learn about plants is to see them as a whole. He should get the feeling of mass. Then he should endeavor to determine why the mass is so and so. Trees are best to begin on. No two trees are alike. How do they differ? The pupil can observe as he comes and goes from school. An orchard of different kinds of fruits shows strong con- trasts. Even different varieties of the same fruit may be unlike in habit. This is especially true in pears (Figs. 101, 102). A honey locust tree, CHAPTER XI HOW THE PLANT TAKES IN THE SOIL WATER 135. PLANT-FOOD.— Having learned what a plant is and having seen it as a whole, we may now inquire how it secures food with which to live. We can discuss only the outlines of the subject here: the pupil may consider the question again when he takes up Part HI. The plant obtains food materials from the soil. We know this to be true, because the plant dies if removed from the soil. In this discussion, we use the word food to designate any material which the plant takes in to incorporate with its tissues or to aid in promoting its vital activities. The word is sometimes used to denote only some of the products (as starch) which the plant manufactures from the raw ma- terials, but it is unfortunate to press a common-language word into such technical use. 136. ROOT STRUCTURE.— Roots divide if srg into the thinnest and finest fibrils : (a Oe there are roots and there are rootlets. 3x 5 The large, fleshy root of the radish (Fig. 103) terminates in a common-sized root to which little rootlets are at- tached. Then there are little rootlets attached to the fleshy root at various places near the base. But the rootlets which we see are only intermediary, and there are numerous yet smaller structures. 137. The rootlets, or fine divisions, are clothed with root- hairs (29), which are very delicate structures. Carefully (64) 103. Root and rootlets. ROOT STRUCTURE 65 germinate radish or other seed, so that no delicate parts of the root will be injured. For this purpose, place a few seeds in packing-moss or in the folds of cloth or blotting paper, being careful to keep them moist. In a few days the seed has germinated, and the root has grown an inch or two long. Notice that, excepting at a distance of about a quarter of an inch behind the tip, the root is covered with minute hairs (Figs. 11, 104). They are actu- ally hairs, that is, root-hairs. Touch them and they collapse, they are so delicate. Dip one of the plants in water, and when removed the hairs are not to be seen. The water mats them together along the root and they are no longer evident. Root-hairs usually are destroyed when a plant is pulled out of the soil, be it done ever so carefully. spleen LD ga They cling to the minute particles of covering of root-hairs. gj], Under a microscope, observe how they are flattened when they come in contact with grains of sand (Chapter II). These root-hairs clothe the young rootlets, and a great amount of soil is thus brought into actual contact with the plant. Moot-hairs are not young roots: they soon die. 138. The rootlet and the root-hair differ. The rootlet is a solid, compact structure. The root-hair is a delicate tube (Fig. 105), within the cell-wall of which is contained living matter (protoplasm); and the lining membrane of this wall permits water and substances in solution to pass a in. Being long and tube-like, these root-hairs are espe- cially adapted for taking in the largest quantity of solu- 1D) 66 FOOD FROM THE SOIL tions; and they are the principal means by which plant- food is absorbed from the soil, although the surfaces of the rootlets themselves do their part. Water-plants do not need an abundant system of root-hairs, and such plants depend largely on their rootlets. 139. OSMOSIS.—In order to understand how the water enters the root-hair, it is necessary that we study the physical process known as os- mosis. A salt solution sepa- rated by a membrane from water absorbs some of the water and increases its own volume. First dissolve one ounce of saltpeter, which we may use as a fertilizer solution, in one pint of water, calling this so- lution No. J. For use in ex- periments later on, also dis- solve a piece of saltpeter not 105. Cross section of root, enlarged, larger than a peach pit (about pp asta emit one-seventh ounce) in about one gallon of water, calling this solution No. II. Now fill the tube, C in Fig. 106, almost full of the strong solution I, and tie a piece of animal membrane (hog’s bladder is excellent for this purpose) over the large mouth. A small funnel, with a long stem, may be used if one cannot obtain a tube like C. Then sink the tube, bladder-part down- wards, into a large bottle, A, of water until the level of liquid in the tube stands at the same height as that in the bottle. The tube may be readily secured in this position by passing it through a hole in the cork of the bottle. In a short time, we notice that the liquid in N begins to rise, and in an hour or so it stands as at F, say. This is an important result. The facts are that the liquids tend to diffuse, but the strong solution in N cannot pass OSMOSIS 67 through the bladder as rapidly as the water outside can pass in. Then there is evidently absorption of water and pressure in N which forces the liquid higher than in the bottle. The liquid in N continues to stand higher than in the bottle while this absorption goes on. 140. The cell-sap of the root-hair absorbs water from the soil by osmotic action. The above experiment enables us to understand how the countless little root-hairs act,— each one like the tube N, if only the whole surface of the tube were a bladder membrane, or something acting similarly. The soil water does not contain much of the land’s fertility: that is, it is a very weak solution. The active little root-hair, on the other hand, is always filled with cell-sap, a more concen- trated solution: hence soil water must come in, and along with it come also small quantities of dissolved food materials. Some of these materials may be fertilizers which have been applied to the land. 141. The plant absorbs these solu- tions as long as they are used for the growth of the plant. The salts which are dissolved in the soil water 16. To illustrate osmosis. also diffuse themselves through the membrane of the root-hairs, each ingredient tending independently to be- come as abundant inside the root-hair as outside in the soil water. Once inside the root-hair, these absorbed solutions pass on to root and stem and leaf, to be utilized in growth. As long as they are used, how- ever, more must come into the root-hairs, in order to restore the equilibrium. Thus those substances which are 68 FOOD FROM THE SOIL needed must come in as long as the land can furnish them in soluble form. Absorption was illustrated before by an artificial arrangement because the root-hairs are so small that they cannot be seen readily. But all parts of the root can absorb some water. 142. Fleshy pieces of root or stem will absorb water from weak solutions and become rigid; im strong solutions such fleshy parts will give up their water and become flexi- ble. To experiment further with this principle of absorp- tion, cut several slices of potato tuber about one-eighth of an inch in thickness, and let them le in the air half an hour. Place a few of these slices in some of the strong fertilizer solution I. Place similar pieces in the weak solution II. In half an hour or more, those pieces in the weak solution will be very rigid or stiff (turgid). They will not bend readily when held lengthwise between the fingers. Compare these slices with those in the strong solution, where they are very flexible (flaccid). This bending is evidently due to the fact that those in the strong brine have actually lost some of their water. So the potato tuber could take in soil water con- taining a small amount of food; but if the water contained much food material the potato would actually lose some of the water which it held. 143. These experiments not only demonstrate how the roots absorb water containing plant- \/// | food, but they emphasize the fact that the out- <== 5) side solution must be very dilute in order to 107. Killeaby De absorbed at all. The root-hairs absorb water hood ww which has dissolved only a small amount of plant- tion. food from the richness of the soil, and not such rich solutions as the sap of the plant itself. 144. The plant may be wilted, and even killed by at- tempting to feed it food solutions which are too strong. ROOT-PRESSURE 69 To test this matter, secure a young radish plant (or almost any seedling with several leaves) and insert the roots into a small bottle containing some of the saltpeter solution I. In another bottle place a similar plant with some of the weak solution II. Support the plant in the mouth of the bottle with cotton batting. After standing for a few hours or less it will be noticed that the leaves of the plant in the strong solution begin to wilt, as in Fig. 107. The plant in the weak solu- tion, Fig. 108, is rigid and normal. This further indicates that the growing plant is so constituted as to be able to make use of very dilute solutions only. If we attempted to feed it strong fertilizer solutions, these : strong solutions, instead of being absorbed jog, The plant by the plant, take water from the latter, thrives’ in 8 . : weak solution. causing the plant to wilt. 145. The farmer or gardener knows that he can injure or even kill his plants by adding too much plant-food. Everyone recognizes the value of wood ashes as a ferti- lizer; but no one would dare water his valuable plants with lye, or sow his choice vegetable seeds on an ash bank, however well it might be watered. If there is a potted plant at hand which is of no value, remove some of the soil, add considerable wood ashes, water well, and await the result; or give it a large lump of nitrate of soda. 146. ROOT-PRESSURE.— The activity of the root in absorb- ing water gives rise to considerable force. This force is known as root-pressure. The cause of this pressure is not well understood. The pressure varies in different plants and in the same plant at different times. ‘To illustrate root-pressure, cut off a strong-growing small plant near the ground. By means of a bit of rubber tube, 70 FOOD FROM THE SOIL attach a glass tube with a bore of approximately the diam- eter of the stem. Pour in a little water. Observe the rise of the water due to the pressure from below (Fig. 109). ae Some plants will force the column of water several feet. The water ascends chiefly in the young wood, not between the bark and wood, as commonly supposed. To illustrate yi the path of water-ascent, insert a growing eh shoot in water which is colored with eosin : alt) note the path which the color takes. (Hosin | \ dye may be had of dealers in microscope | i supplies. Common aniline may answer very 1 well. ) 147. HOW THE SOIL HOLDS MOISTURE.— The water which is valuable to the plant is not the free water, but the thin film of moisture which adheres to each little particle of soil. The finer the soil, the greater the number of particles, and therefore the greater is the quantity of film moisture which it ean hold. This moisture surrounding the grains may not be perceptible, yet the plant can use it. Root absorption may continue in a soil which seems to be dust dry. 148. THE ROOTS NEED AIR. — Corn on land which has been flooded by heavy rains loses its green color and turns yellow. Besides diluting plant-food, the water drives the air from the soil, and Z this suffocation of the roots ¢s very soon 109. apparent in the general ill health of the To show root-pressure. HIant, Stirring or tilling the soil aérates it. Water-plants and bog-plants have adapted themselves to their particular conditions. They either get their air by special surface roots, or from the water. PROPER TEMPERATURE—ROOTS EXCRETE vial 149. PROPER TEMPERATURE.—The root must be warm in order to perform its functions. Should the soil of fields or greenhouses be much colder than the air, the plant suffers. When in a warm atmosphere, or in a dry atmos- phere, plants need to absorb much water from the soil, and the roots must be warm if the root-hairs are to supply the water as rapidly as it is needed. Jf the roots are chilled, the plant may wilt or die. Try this with two potted plants, as radish, coleus, tomato, ete. Put one pot in a dish of ice water, and the other in a dish of warm water, and keep them in a warm room. ¥¢ In a short time notice how stiff and vigorous is the one whose roots are warm, whereas the other may show signs of wilting. 150. ROOTS EXCRETE. — The plant not only absorbs what is already solu- ble, but dt is capable of rendering soluble small quantities of the insoluble substances present in the soil, and which may be needed for plant-food. The plant accomplishes this result by means of certain acid excretions from the roots. These acids may even etch marble. On a polished marble block, place a half-inch of sawdust or soil, in which plant seeds. After the plants have attained a few leaves, turn the mass of sawdust over and observe the ? 110. The rootlets and root- prints of the roots on the marble. hairs cling to the particles These prints will be very faint. An ° sel. illustration of this experiment is given on page 73. Care- fully pull up a young seedling which is growing in soft soil, and notice how tenaciously the soil particles are held to the root (Fig. 110). ip FOOD FROM THE SOIL 151. THE FOOD MATERIALS.—We have seen that all food materials must be in solution in water in order to be taken in by the roots. Different kinds of plants require different kinds and proportions of the food materials, but ordinary green plants are supposed to require at least eleven of the elementary substances in order to live. These are: Carbon, C. Potassium, K. Oxygen, O. Calcium, Ca. Nitrogen, N. Magnesium, Mg. Hydrogen, H. Phosphorus, P. Sulfur, S. Iron, Fe. Chlorine, Cl. (in some plants). All these elements must be in combinations, not in their elemental form, in order to be absorbed by roots. 152. Usually all of these except carbon and oxygen are taken in only through the roots. Some of the oxygen is taken in by the roots in the form of water (which is H20), and in other compounds. Some carbon is probably taken in by the roots in the form of carbonates, but it is doubt- ful whether this source of carbon is important to the plant. Water is not only a earrier of plant-food: it is itself a plant-food, for some of it is used in the building up of organic materials. The seven elements in the right-hand column are ealled the mineral elements: they remain in the ash, when the plant is burned. The mineral elements come from the soil. 153. The ash is a small part of the total weight of the plant. In a eorn plant of the roasting-ear stage, the ash (what remains after ordinary burning) is about 1 per cent of the total substance. 154. Water is the most abundant single constituent or substance of plants. In the corn plant of the roasting- ld) WATER IN THE PLANT fo ear stage, about 80 per cent of the substance is water. A fresh turnip is over 90 per cent water. Fresh wood of the apple contains about 45 per cent of water. The plant secures its water from the soil. Review.—What is plant-food? Where does some of it come from? Describe the feeding root. Describe root-hairs. What is their function? How does the root-hair differ from the rootlet ? What is osmosis? Describe the experiment. How does the soil water get into the root-hair? For how long does this absorption continue? Under what conditions may the root-hair lose its sap? In what condi- tion must the soil water be in order to be absorbed? What may result if the food solutions are too strong? Has this fact any interest to the plant-grower? What is root-pressure? How is the water held in the soil when it is most valuable to the plant? How are plants able to live in dry soil? Why do roots need air? How do they get it? Deseribe what effect a cold soil has on roots. How do roots secure the plant- food in the soil particles? What elements are necessary to plants? In what forms must these elements be in order to be absorbed by the roots? About what percentage of the whole substance is ash? What is the most abundant constituent in plants? Whence does it come? Notre.—Examine soil under a lens, to see the odd and miscel- laneous particles of which it is composed. Not all kinds of plants exhibit strong root-pressure. The grape vine is a good subject to show it. If pot plants are used, choose a well-rooted one with a straight stem. Coleus, begonia and Impatiens Sultani are good subjects. These can be had at greenhouses. a4 =) a , ) Root excretions may etch a marble surface, CHAPTER XII THE MAKING OF THE LIVING MATTER 155. SOURCES OF FOOD.—The ordinary green plant has but two sources from which to obtain food,—the air and the soil. When a plant is thoroughly dried in an oven, the water passes off: this water came from the soil (154). The remaining part is called the dry substance or dry matter. If the dry matter is burned in an ordinary fire, only the ash remains: this ash came from the soil (152).. The part which passed off as gas in the burning contained the elements which came from the air: it also contained some of those which came from the soil—all those (as nitrogen, hydrogen, chlorine) which are transformed into gases by the heat of a common fire. 156. CARBON.—Carbon enters abundantly into the com- position of all plants. Note what happens when a plant is burned without free access of air, or smothered, as in a chareoal pit. A mass of charcoal remains, almost as large as the body of the plant. Charcoal is almost pure carbon, the ash present being so small in proportion to the large amount of carbon that we look on the ash as an im- purity. Half or more of the dry substance of a tree is carbon. When the tree is charred (or incompletely burned), the carbon remains in the form of chareoal. The carbon goes off as a gas when the plant is burned in air. It does not go off alone, but in combination with oxygen, and in the form ealled carbon dioxid gas, COsz. 157. The green plant secures its carbon from the air. In other words, much of the solid matter of the plant comes from one of the gases. By volume carbon diorid (74) ae (- CHLOROPHYLL forms only about three-hundredths of 1 per cent of the air. It would be very disastrous to animal life, however, if this percentage were much increased, for it excludes the life- giving oxygen. Carbon dioxid is often called “foul-gas.” It may accumulate in old wells, and an experienced person will not descend into such wells until they have been tested with atoreh. If the air in the well will not support com- bustion, that is, if the torch is extinguished, it usually means that carbon dioxid has drained into the place. The air of a closed school-room often contains far too much of this gas along with little solid particles of waste matters. Carbon dioxid is often known as carbonic acid gas. 158. APPROPRIATION OF THE CARBON.— The carbon di- oxid of the air readily diffuses into the leaves and other green parts of the plant. The leaf is delicate in texture, and often the air can enter directly into the leaf tissues. There are, however, special inlets provided for the admis- sion of gases into the leaves and other green parts. These inlets consist of numerous pores (stomates or stomata), which are especially abundant on the under surface of the leaf. The apple leaf contains about one hundred thousand of these pores to each square inch of the under surface. Through these breathing pores the outside air enters into the air-spaces of the plant, and finally into the little cells containing the living matter. In Part III these breathing pores will be studied. 159, CHLOROPHYLL.— The green color of leaves is due to a substance called chlorophyll. Purchase at the drug store about a gill of wood aleohol. Secure a leaf of geranium, clover, or other plant which has been exposed to sun- light for a few hours and, after dipping it for a minute in boiling water, put it in a white eup with sufficient aleohol to cover the leaf. Place the cup on the stove Where it is not hot enough for the aleohol to take fire. After a time the chlorophyll is dissolved by the alcohol, 76 THE MAKING OF THE LIVING MATTER which has become an intense green. Save this leaf for a future experiment. Without chlorophyll, the plant can not appropriate the carbon dioxid of the air. 160. In most plants this chlorophyll or leaf-green is seattered throughout the green tissues in little oval bodies, and these bodies are most abundant near the upper surface of the leaf, where they can secure the greatest amount of light. Without this green coloring matter, there would be no reason for the large flat surfaces which the leaves possess, and no reason for the fact that the leaves are borne most abundently at the ends of branches, where the light is most available. Plants with colored leaves, as coleus, have chlorophyll, but it is masked by other color- ing matter. This other coloring matter is usually soluble in hot water: boil a coleus leaf and notice that it becomes green and the water becomes colored. 161. Plants grown in darkness are yellow and slender, and do not reach maturity. Compare the potato sprouts which have grown from a tuber lying in the dark cellar with those which have grown normally in the bright light (Fig. 42). The shoots have reached out for that which they cannot find; and when the food which is stored in the tuber is exhausted, these shoots will have lived useless lives. A plant which has been grown in darkness from the seed will soon die, although for a time the little seedling will grow very tall and slender. Light makes possible the production of chlorophyll. Sometimes chlorophyll is found in buds and seeds, but it is probable that these places are not perfectly dark. Notice how potato tubers develop chlorophyll, or become green, when exposed to lght. 162. PHOTOSYNTHESIS.—Carbon dioxid is absorbed by the leaf during sunlight, and oxygen is given off. We have seen (157) that carbon dioxid will not support animal life. Experiments have shown that carbon diorid is ab- sorbed and that oxygen is given off by all green surfaces STARCH ea of plants during the hours of sunlight. How the ear- bon dioxid which is thus absorbed may be used as food is a complex question, and need not be studied here. 163. Chlorophyll absorbs the heat of the sun’s rays, and the energy thus obtained is used by the living matter in unit- ing the carbon dioxid absorbed from the air with some of the water brought up by the roots. The process by which these compounds are united is a complex one, but the ultimate result usually is starch. No one knows all the details of this process; and our first definite knowledge of the product be- gins when starch is deposited in the leaves. The process of using the carbon dioxid of the air has been known as carbon-assimilation, but the term now most used is photo- synthesis (from Greek words, meaning light and to put to- gether). 164. STARCH.—AI] starch is composed of carbon, hydro- gen, and oxygen (Ce6HwOs). The sugars and the woody substances are very similar to it in composition. All these substances are called carbo- hydrates. In making this starch from the carbon and oxygen of carbon dioxid and lll. To show the escape of oxygen. from the hydrogen and oxygen of the water, there is a sur- plus of orygen. It is this oxygen which is given off into the air. To test the giving off of oxygen by day, make the experiment illustrated in Fig. 111. Under a funnel in a 78 THE MAKING OF THE LIVING MATTER deep glass jar containing fresh spring or stream water, place fresh pieces of the common water-weed elodea (or anacharis). Invert a test tube over the stem of the fun- nel. In sunlight bubbles of oxygen will arise and collect in the test tube. When a sufficient quantity of oxygen has collected, a lighted taper inserted in the tube will glow with a brighter flame, showing the presence of oxygen. ~* : A) ply to the plant sufficient water to a equalize that transpired by the 117. To illustrate transpiration. leaves, the plant wilts. Transpiration from the leaves and delicate shoots is increased by all of the conditions which would increase evaporation, such as higher temperature, dry air or wind. The breathing pores are so constructed that they open and close with the varying conditions of the atmosphere, and thereby regulate transpiration. However, during periods of drought or of very hot weather, and especially during a hot wind, the closing of these stomates cannot sufficiently prevent evaporation. The roots may be very active and yet fail to absorb sufficient moisture to equalize that given off by the leaves. The plant wilts. Any injury to the roots or even chilling them (149) may cause the plant to wilt. Ona hot, dry day note how the leaves of corn “roll” towards afternoon, Early the fol- lowing morning note how fresh and vigorous the same leaves appear. Water is also forced up by root-pressure (146). Some of the dew on the grass in the morning 84 THE MAKING OF THE LIVING MATTER may be the water forced up by the roots; some of it is the condensed vapor of the air. 176. The wilting of a plant is due to the loss of water from the cells. The cell walls are soft, and collapse. ally buds are borne in their axils. (3) Leaves are usually borne at joints or nodes. (4) They arise on wood of the current-year’s 143. Muskmelon seedlings, with the un- growth. (5) They have a like seed-leaves and true leaves. more or less definite arrangement. When leaves fall, the twig which bore them remains; when leaflets fall, the main petiole which bore them falls also. 144. A leaf mosaic of Norway maple. Note the varying lengths of petioles. 145. Shoot of the common white pin , one-third natural size. The picture shows the falling of the leaves from the different years’ growth. The part of the branch between the tip and A is the last season’s growth; between A and B it is two years old; the part between B and © is three years old; it has few leaves, The part that grew four seasons ago—beyond C—has no leaves, 100 LEAVES AND FOLIAGE ReEvViEw.—How may leaves be studied? What is meant by func- tion? What do leaves do? What other parts may perform the function of leaves? How is form of leaves associated with their function? What are simple leaves? Com- pound? What is venation? What are the types or kinds of venation? What are the two types of compound leaves? What is a leaflet? Define bi- compound ; deecompound. What are lobed, cleft, parted, and divided leaves? Pinnatifid leaf ? Com- plete leaf? Complete leaflet? What is a sessile leaf? How may the petiole join the blade? How are the shapes of leaves named or classified? De- fine the shapes described in 198. Describe com- 116. Oblique leaf of | mon shapes of the base of the leaf. Of the apex. UBSGIDS. Of the margin. How are the forms and sizes of leaves ever related to theiplace in which they grow? Why do leaves fall? Define deciduous. Persistent. Evergreen. When do pine leaves fall? How can you distinguish leaves? Describe the leaf in Fig. 146. The same lilac bushes in January and July.—Framework and foliage. CHAPTER XV MORPHOLOGY, OR THE STUDY OF THE FORMS OF PLANT MEMBERS 208. Botanists interpret all parts of the plant in terms of root, stem, and leaf. That is, the various parts, as thorns, flowers, fruits, bud-scales, tendrils, and abnormal or unusual members, are supposed to represent or to stand in the place of roots, stems (branches), or leaves. 209. The forms of the parts of plants are interesting, therefore, in three ways: (1) merely as forms, which may be named and deseribed; (2) their relation to function, or how they enable the part better to live and work; (3) their origin, as to how they came to be and whether they have been produced by the transformation of other parts. The whole study of forms is known as morphology (literally, the “science of forms”). We may consider examples in the study of morphology. 210. It is customary to say that the various parts of plants are transformed or modified root, stem, or leaf, but the words transformation and modification are not used in the literal sense. It is meant that the given part, as a ten- dril, may occupy the place of orrepresent a leaf. It was not first a leaf and then a tendril, but was a tendril from the first: the part develops into a tendril instead of into a leaf: it stands where a leaf normally might have stood. 211. It is better to say that parts which have similar origins, which arise from the same fundamental type, or which are of close genealogical relationship, are homolo- gous. Thus the tendril, in the instance assumed above, is homologous with a leaf. Parts which have similar fune- (101) 102 MORPHOLOGY tions or perform similar labor, without respect to origins, are analogous. Thus a leaf-tendril is analogous to a branech-tendril, but the two are not homo- logous. 212. There are five tests by means of which we may hope to determine what a given part is: (1) by the appearance or %, looks of the part (the least reli- ~~ able test); (2) by the position of the part with relation to other parts —its place on the plant; (3) by comparison with similar 147. Leaf and clad- ; ophyllaofaspar. Parts on other plants (compara- 18. Leaves of agus, tive morphology); (4) by study of **P#"#8"5- intermediate or connecting parts; (5) by study of the development of the part in the bud or as it originates, by means of the microscope (embryology). The last test can be applied only by the trained investigator, but it often gives the most conclusive evidence. Even with 149. Fern-like leaf-branches of a greenhouse asparagus. the appheation of all these tests, it is sometimes im- possible to arrive at a definite conelusion as to the origin or morphology of a part. For example, it is not yet agreed whether most cactus spines represent leaves or CLADOPHYLLA _ 103 branches, or are mere outgrowths of the epidermis (as hairs are). 213. The foliage of asparagus is com- posed of modified branches. The true leaves of asparagus are minute whitish seales (a, Fig. 147). V The green foliage is produced in the axils of these scales. On the strong spring SZ — shoots of asparagus, which are eaten, the true leaves appear as large 151, Phyllodia of aea- seales (a, a, Fig. 148). These large Gily Dee vere an scales persist on the base of ayaa etaas nTBes, the asparagus plant, even in the fall. In the spe- cies of greenhouse or ornamental asparagus, the \ delicate foliage is also made up of green leaf-like \ branches (Fig. 149). In some cases the true leaves fall after a time, and there is little evidence left. The strong new shoots usually show the true leaves plainly (as in Fig. 150). Branches which simulate leaves are known as cladophylla (singular, cladophyllum). The broad flat leaves of florists’ smilax (common in glass- houses) are cladophylla. 214. In the study of morphology, it is not enough, however, merely to 150. Strong new shoot of Asparagus Sprengeri, showing the true leaves and the branches springing from their axils. determine whether a part represents root, stem, or leaf: one must determine what part or kind of root, stem, or leaf 104 MORPHOLOGY it stands for. For example, the foliage in Fig. 151 represents green expanded petioles. These leaf-like mem- bers bear buds (which produce branches) in their axils, and they have the arrangement or phyllo- taxy of leaves; therefore they are considered to be true leaf parts. But they stand edgewise as if 152. The thorns are in the axils they might be petioles; sometimes of leaves. cias have compound expanded leaves; there are intermediate forms or grada- tions between different acacias; young seedlings sometimes show intermediate forms. From all the evidence, it is now understood that the foliage of the simple- leaf acacias represents leaf-like petioles. Such petioles are known as phyllodia they bear leaf-blades; other aca- (singular, phyllodium) : 153. Two or more buds 154. Some of the buds pro- duce leafy branches. normal leafy branches (Fig. 154); sometimes the thorn itself bears leaves (Fig. 155). The thorns of wilding pears, apples, and plums are short, hardened branches. In well-cultivated trees there is sufficient vigor 915. Thorns are borne in the axils. and strong spines are usually branches. The spines of hawthorns or thorn-apples are examples: they are borne in the axils of leaves as branches are (Fig. 152); hawthorns usually bear two or more buds in each axil (Fig. 153), and one or two of these buds often grow the following year into = : 155. The thorn to push the main branch into longer and may bearieaves. PRICKLES AND BRISTLES 105 softer growth, so that the side buds do not have a chance to start. The thorns of osage orange and honey locust are also branches. Those of the honey locust usually arise from supernumerary buds which are borne somewhat above the axils. 216. Prickles, bristles, and weak spines, which have a definite arrangement on the stem, are usually modified leaves or parts of leaves. The spines of 156. Leaf-spine of thistles are hardened BAUBeEy, points of leaf-lobes. The spines of the barberry are reduced leaves; in their axils are borne short branches or leaf-tufts (Fig. 156); in spring on young shoots may be found almost complete gradations from spiny leaves to spines. In the prickly ash the prickles are stipules and stipels. The reasons for interpreting them so are apparent in Fig. 157. Stipular prickles may also be seen in the common or aca- cia locust (robinia). 217. Prickles, bristles, and hairs, which are scattered or 157. Stipular prickles Wave no definiie ar- AN of prickly ash. = rangement, are USU- f \4, ully mere out-growths of the epi- pw \\\/ dermis. They usually are re- moved with the bark. Of such are the prickles of squashes, briars (Fig. 158), and roses. 218. The reason for the exis- 2 aa tence of spines is difficult to de- ray 158. Prickles of dewberry. termine. In many or most cases they seem to have no distinct use or function. In some way they are associated with the evolution of the plant, 106 MORPHOLOGY and one cannot determine why they came without know- ing much of the genealogy of the plant. In some cases they seem to be the result of the contraction of the plant-body, as in the cacti and other desert plants; and they may then serve a purpose in lessening transpiration. It is a common notion that spines and prickles exist for the purpose of keep- ing enemies away, and that hairs keep the plant warm, but these ideas usually lack scientific accuracy. Even if spines do keep away browsing ani- mals in any plant, it is quite another question why the spines came to be. 159, The diminishing leaves To answer the question what spines of ponescl: and hairs are for demands close scientific study of each particular case, as any other problem does. 219. Leaves are usually smaller as they approach the flowers (Fig. 159). They often become so much reduced as to be mere scales, losing their office as foliage. In their axils, however, the flower-branches may be borne (Fig. 160). Much-reduced leaves, particularly those which are no longer green and working members, are called bracts. In some cases, 160, The uppermost flowers are Pomme’ lanes colored. bracts are wore in the axils of bracts.—Fuchsia. just beneath the flowers and look like petals: the flowering dogwood is an example ; also the bougainvillea, which is common in glasshouses SCALES OF BUDS AND. BULBS 107 (Fig. 161); also the scarlet sage of gardens and the flaming poinsettia of greenhouses. 220. The scales of buds are special kinds of bracts. In some cases each scale represents an entire leaf; in others, it represents a petiole or stipule. In the expanding pear, maple, lilac, hickory, and horse-chestnut buds, note the gradation from dry scales to green leaf-like bodies. When the winter scales fall by the pushing out of the young shoot, scars are left: these scars form “rings,” which mark the annual growths. See Chap. VII. The scales of bulbs are also special kinds of leaves or bracts. In some cases they are merely protective bodies; in others j¢ . In the bougainvillea three gaudily they are storehouses. We colored bracts surround each clus- ter of three small flowers. have found (45) that the presence of scales or bracts is one means of distinguish- ing underground stems from roots. Review.— What are considered to be the fundamental or type forms from which the parts of plants are derived? How do the forms of plants interest us? What is morphology? What is meant by trans- formation and modification as used by the morphologist ? What is meant by homologous parts? Analogous parts? Tell how one may determine the morphology of any part. What is a cladophyllum ? Phyllodium? Show a specimen of one or the other, or both (canned asparagus can always be had in the market). What is the morphology of most thorns? Explain the thorns of hawthorn. What are bristles, prickles, and hairs? Why do spines and bristles exist? Explain what a bract is. A bud-seale. A bulb-seale. CHAPTER XVI HOW PLANTS CLIMB 221. We have seen that plants struggle or contend for a place in which to live. Some of them become adapted to grow in the forest shade, others to grow on other plants as epiphytes, others to climb to the light. Observe how woods grapes, and other forest climbers, spread their foli- age on the very top of the forest tree, while their long flexile trunks may be bare. 222. There are several ways in which plants climb, but most climbers may be classified into four groups: (1) scram- blers, (2) root-climbers, (3) tendril-climbers, (4) twiners. 223. SCRAMBLERS.— Some plants rise to ight and air by resting their long and weak stems on the tops of bushes and quick-growing herbs. Their stems are ele- vated by the growing twigs of the plants on which they recline. Such plants are seramblers. Usually they are provided with prickles or bristles. In most weedy swamp thickets, scramb- ling plants may be found. Briars, some roses, bed- straw or galium, bitter- sweet (Solanum Duleamara, not the celastrus), the tear-thumb polygonums, and other plants are familiar examples of scramblers. 224. ROOT-CLIMBERS.— Some plants climb by means of true roots, as explained in paragraph 31. These roots (108) 162. A root-climber.—The English ivy. TENDRIL - CLIMBERS 109 seek the dark places and therefore enter the chinks in walls and bark. Fig. 12, the trumpet creeper, is a fa- miliar example. The true or English ivy, which is often grown to cover buildings, is another instance (Fig. 162). Still another is the poison ivy. Roots are distinguished from stem tendrils by their irregular or indefinite posi- tion as well as by their mode of growth. 225. TENDRIL-CLIMBERS.— A slender coiling part which serves to hold a climbing plant to a support is known as a AY 163. Tendril of Virginia creeper. The direction of the coil changes near the middle tendril. The free end swings or curves until if strikes some object, when it attaches itself and then coils and draws the plant close to the support. The spring of the coil also allows the plant to move in the wind, thereby enabling the plant to maintain its hold. Slowly pull a well-ma- tured tendril from its support, and note how strongly it holds on. Watch the tendrils in a storm. ‘To test the movement of a free tendril, draw an ink line lengthwise of it, and note that the line is now on the coneave side and now on the convex side. Of course this movement is slow, but it is often evident in an hour or so. Usually the tendril attaches to the support by coiling about it, but the Virginia ereeper and Boston ivy attach to walls by means of disks on the ends of the tendrils. 226. Since both ends of the tendril are fixed, when it 110 HOW PLANTS CLIMB finds a support, the coiling would tend to twist it in two. It will be found, however, that the tendril coils in differ- ent directions in different parts of its length. In Fig. 163 the change of direction in the coil occurs at the straight place near the middle. In long tendrils of cueum- bers and melons there may be several changes of direction. 227. Tendrils may be either branches or leaves. In 164. The fruit-cluster and tendril of grape are homologous. the Virginia creeper and grape they are branches; they stand opposite the leaves in the position of fruit-clusters (Fie. 164), and sometimes one branch of a fruit-cluster is a tendril. These tendrils are therefore homologous with fruit-clusters, and fruit-clusters are branches. 228. In some plants tendrils are leaflets. Examples are the sweet pea (Fig. 165) and common garden pea. In Fig. 165, observe the leaf with its two stipules, petiole, TENDRIL - CLIMBERS Bel two normal leaflets, and two or three pairs of leaflet- tendrils and a terminal leaflet-tendril. The cobea, a common garden elimber, has a similar arrangement. In some cases tendrils are stipules, as probably in the green- briars (smilax). 229, The petiole or midrib may act as a tendril, as in various kinds of clematis. In Fig. 166, two opposite leaves 165. In the sweet pea (and garden pea) the leaflets are tendrils. are attached at a. Each leaf is pinnately compound and has two pairs of leaflets and a terminal leaflet. At ) and ¢ the midrib or rachis has wound about a support. The petiole and the petiolules may behave similarly. Examine the tall-growing nasturtiums in the garden, 230. TWINERS.—The entire plant or shoot may wind about a support. Such a plant is a twiner. Examples are bean, hop, morning-glory, moon-flower, false bitter- 112 HOW PLANTS CLIMB sweet or wax-work (celastrus), some honeysuckles, wis- taria, Dutchman’s pipe, dodder. The free tip of the twining branch sweeps about in curves, much as the tendril does, until it finds support or becomes old and rigid. 231. Hach kind of plant usually coils in only one pay 166. Clematis climbs by means of its leaf-stalks direction. Most plants coil against the sun, or from the observer’s left across his front to his right as he faces the plant. Such plants are said to be dextrorse (right-handed ) or antitropic (against the sun). Examples are bean, morn- ing-glory. The hop twines from the observer’s right to his left. Such plants are sinistrorse (left-handed) or REVIEW ON CLIMBING 167. Dextrorse and sinistrorse twiners.—False bitter-sweet and hop. understand why the branch (as tendril and stands opposite the bud in the grape and Virginia creeper. Note that a grape-shoot ends in a tendril The tendril represents the true axis of the shoot. side a leaf is borne, from the axil of which the branch grows to continue the shoot, This branch ends in a tendril, b}. Another leaf has a branch in its axil, and this branch ends in the tendril ¢. real apex of the shoot is successively turned until it appears to be lateral. Thatis, the morpho- logically terminal points of the successive shoots are the tendrils, and the order of their appearing is a, b,c. The tendrils branch: observe the minute representing a leaf at the base of each branch. type of branching—the axial growth being continued by suecessive lateral buds—is sympodial, and the branch is a sympode. Continuous growth from the PLANTS 113 eutropic (with the sun). Fig.167 shows the two directions. REVIEW.— Why do plants climb? How do they climb? Explain what is meant by scram- blers. By roct-climbers. What is a tendril? How does it find a support? Why and how does it coil? How does it grasp itssupport? What is the morphology of the ten- dril of Virginia creeper? Why? Of the pea? Of the clematis? What is a twiner? How does it find asupport? What is a dex- trorse twiner? Sinistrorse? NOTE.- -The : d e pupil may not flower-cluster) (a, Fig. 168). On the The aside seale This L168. Sympode of the grape terminal bud is monopodial, and the branch is a monopode. H CHAPTER XVII FLOWER-BRANCHES 932. We have (86) seen that branches arise from the axils of leaves. Sometimes the leaves may be reduced to bracts and yet branches 169. Terminal flowers of the white- weed (in some places called ox-eye daisy). are borne in theiraxils. Some of the branches grow into long limbs; others become short spurs; others bear flowers. 233. Flowers are usually borne near the top of the plant, since the plant must grow before it blooms. Often they are produced in great numbers. It results, therefore, that flower - branches usually stand close together, form- ing a cluster. The shape and arrangement of the flower-cluster differ with the kind of plant, since each plant has its own mode of branching. 234. Certain definite or well- marked types of flower-clusters have received names. Some of these names we shall discuss, but the flower-clusters which perfectly match the definitions are the ex- ception rather than the rule. The determining of the kinds of flow- er-clusters is one of the most per- (114) SOLITARY FLOWERS—CORYMBOSE CLUSTERS 115 plexing subjects in descriptive botany. We may classify the subject around three ideas: solitary flowers, corym- bose clusters, cymose clus- ters. 235. SOLITARY FLOWERS. — In many eases flowers are borne singly. They are then said to be solitary. The solitary flower may be either at the end of the main shoot or axis (Fig. 169), when it is said to be terminal, or from the side of the shoot (Fig. 170), when it is said to be lateral. The lateral flower is also said to be axillary. 236. CORYMBOSE CLUSTERS.— If the flower-bearing axils were rather close together, an open or leafy flower-cluster might re- sult, as in Fig. 171. The fuchsia continues to grow from the tip, and the older flowers are left farther and farther behind. If the cluster were so ay short as to be flat or convex on Mh top, the outermost flowers would | be the older. A flower-cluster | in which the lower or outer flow- ers open first is said to be a corymbose cluster. It is some- times said to be an indetermi- nate cluster, since it is the re- 170. Lateral flower of abutilon. sult of a type of growth which may go on more or less contin- | ‘ | uously from the apex. 171. Leaty tlower-cluster of fuchsia 237. The simplest form of a definite corymbose cluster is a raceme, which is an unbranched open cluster in which 116 FLOWER - BRANCHES the flowers are borne on short stems and open from below (that is, from the older part of the shoot) upwards. The raceme may be terminal to the main branch, as in Fig. 172, or it may be lateral to it, as in Fig. 178. Racemes often bear the flowers on one side of the stem, or in a single row. 238. When a corymbose flower- cluster is long and dense and the flowers are sessile or nearly so, it is called a spike. (Migs) 74, 2145) Common examples of spikes are plantain, mignonette, mullein. 239. A very short and dense spike is a head. Clover (Fig. 176) is a good exam- ple. The sunflower and re- lated plants bear many small flowers in a very dense head. This special kind of head of the sunflower, thistle, and aster tribes has been called an anthodium, but 4 Bs { r this word is little NG iss aR y used. Note that We SAF YANG 172. Terminal racemes of dicentra. in the sunflower (Fig. 177) the out- side or. exterior ’ fp flowers open first. AS GY 9 Another gs pee lal 173. Lateral racemes (in fruit) of barberry. form of spike is the catkin, which usually has scaly bracts and the whole cluster is deciduous after flowering or fruit- CORYMBOSE CLUSTERS 117 ing, and the flowers (in | vs nT ‘| tt tava) typical cases) have only one sex. Examples are the“ pussies” of willows (Fig. 213) and flower- clusters of oaks (Fig. 212), hickories, poplars. 240. When a loose, elongated corymbose flower-cluster branches, or is compound, it is called a panicle. Be- cause of the earler 175. Loose spikes of false dragon’s head or physo- growth of the lower branches, the panicle is seal usually broadest at the base or conical in out- 174. Spike of hyacinth. ~ . 4 P sel cic eters - 7 Note, also, line. True panicles are not common. Pree aie flowers and foliage are pro d uced from the stored food a corymb (Fig. 178). The outermost flowers oo nt open first. Fig. 179 shows many corymbs of — ?uly, water the bridal wreath, one of the spireas. 242. When the branches of an indeterminate 941. When an indeterminate flower-cluster is short, so that the top is convex or flat, it is cluster arise from a common point, like the frame of an um- brella, the clus- ter is an umbel (Fig.180). Typi- cal umbels occur in carrot, par- snip, parsley and other plants of the parsley fam- ily: the family Head of crimson clover, 177 Head of sunflower, Is known is the 118 TLOWER- BRANCHES Umbellifere, or umbel- bearing family. In the carrot and many other Um- belliferee, there are small or secondary umbels, called umbellets, at the end of each of the main branches. (In the center of the wild carrot umbel one often finds a single, blackish, often aborted flower, comprising a 1- flowered umbellet. ) 243. CYMOSE CLUSTERS. USAR Nav Mp — When the terminal or 179. Corymbs of the bridal wreath (spirea). central flower opens first, the cluster is said to be cymose. The growth of the shoot or cluster is determinate, since the length is definitely determined or stopped by the terminal flower. Fig. 181 shows a determinate or cymose mode of flower-bearing. 244. Dense cymose clusters are usually flattish on top because of the cessation of growth in the main or central axis. These com- pact flower-clusters are known as cymes. Apples, pears (Fig. 182) and cherries bear flowers in cymes. Some cymes look very like umbels (as in Fig. 183). A head-like cymose eluster is a glomerule: it blooms from the top downwards rather than from 178. Corymb of eandytutt, the base upwards. MIXED CLUSTERS — INFLORESCENCE 119 245. MIXED CLUSTERS .— Often the cluster is mixed, being <3 determinate in one part and in- determinate in another part of the same cluster. This is the case in Fig. 184. The main clus- ter is indeterminate, but the branches are determinate. The es Seek cluster has the appearance of a wild carrot. panicle, and is usually so called, but it is really a thyrse. Lilac is a familiar example of a thyrse. In See? some eases, the main cluster is de- terminate and the branches are in- determinate, as in hydrangea and elder. Such clusters are corym- bose cymes. 246. INFLORESCENCE.—The mode or method of flower arrangement is known as the inflorescence. That is, the inflorescence is cymose, corymbose, paniculate, spieate, soli- tary. sy custom, however, the word inflorescence has come to be used for the flower-cluster itself in works on descriptive botany. Thus a cyme or a : 181. Determinate or cymose panicle may arrangement, — Wild geranium. be called an inflorescence. It will be seen that even solitary flowers follow either indeterminate or determinate meth- ods of branching. 247, THE FLOWER-STEM.— The 182. Cyme of pear. stem of a solitary flower is known as Compare Fig. 63, 120 FLOWER-BRANCHES 183, An umbel-like cyme.—Geranium. a peduncle; also the general stem of a flower- cluster. The stem of the individual flower in a cluster is a pedicel. 248. In the so-ealled stemless plants (37) the peduncle may arise di- rectly from the ground, or crown of the plant, as in dandelion, hya- einth (Fig. 174), gar- den daisy (Fig. 185). This kind of peduncle is; Calledtal scapes: — scape may bear one or many flowers. It has no foliage leaves, but it may have bracts. Revyirw.— What is the homology of flower-branches? How is it that flowers are often borne in clusters? Explain what may be meant by a solitary flower. What are the two types of flower-clus- ters? What are corymbose clus- ters? Define raceme. Spike. Head and anthodium. Catkin. Panicle. Umbel. Umbellet. Corymb. What are eymose clus- ters? What is a cyme? Glome- rule? Contrast indeterminate and determinate modes of branching. Explain mixed elusters. What is a thyrse? What is meant by Define peduncle, pedicel, and scape. the word inflorescence? Note.—In the study of flower- clusters, it is well to select first 184. Thyrse of horse-chestnut. REVIEW ON 185. Scapes of the true or English daisy. and determine the method of this inflorescence, In some eases the flower-cluster ends in a leaf, suggesting that the cluster is morphologically ¢ leaf; but see whether there is not a joint between the cluster and the leaf, showing that the attached to The flower-cluster of the tomato leaf is a branch. has been greatly modified by cultivation. It was originally distinetly racemose. FLOWER-BRANCHES 121 those which are fairly typical of the the various classes discussed in the preceding paragraphs. As soon as the main types are well fixed in the mind, random clusters should be examined, for the pupil must never receive the impression that all flower-clusters follow the defini- tions Clusters of the commonest plants are very puzzling, but the pupil should at least be able to discover whether the inflorescence is determinate or indeterminate. In the tomato (Fig. 186) the flower-cluster is opposite the leaf. Examine blooming tomato plants, in books. of some Compare the grape. 186. Tomato shoot. Geraniums in the s¢ hool-room window CHAPTER XVIII THE PARTS OF THE FLOWER 249. The flower exists for the purpose of producing seed. It is probable that all its varied forms and colors contribute to this supreme end. These forms and colors please the human faney and make living the happier, but the flower exists for the good of the plant, not for the good of man. The parts of the flower are of two general kinds — those which are directly concerned in the produc- tion of seeds, and those which act as covering and pro- tecting organs. The former parts are known as the essen- tial organs; the latter as the floral envelopes. 250. ENVELOPES.—The floral envelopes usually bear a close resemblance to leaves. These envelopes are very commonly of two series or kinds —the outer and the inner. The outer series, known as the calyx, is usually smaller and green. It usually comprises the outer cover of the flower-bud. The calyx is the lowest whorl in Fig. 187. The inner series, known as the corolla, is usually colored and more special or irregular in shape than the 187. Flower of a buttercup calyx. It 1S the bs in section. showy part of the 188. Flower of buttercup. flower, as a rule. The corolla is the second or large whorl in Fig. 187. It is the large part in Fig. 188. 251. The calyx may be composed of several leaves. Each leaf is a sepal. If it is of one piece, it may be (122) FLORAL ENVELOPES BR: lobed or divided, in which ease the divisions are called calyx-lobes. In lke manner, the corolla may be com- posed of petals, or it may be of one piece and variously lobed. A calyx of one piece, no matter how deeply lobed, is gamosepalous. A corolla of one piece is gamopetal- ous. When these series are of separate pieces, as in Fig. 187, the flower is said to be polysepalous and polypetalous. Sometimes both series are of separate parts, and sometimes only one of them is so formed. 252. The floral envelopes are homologous with leaves. Sepals and petals, at least when more than three or five, are each in more than one whorl, and one whorl stands below another so that the parts overlap. They are borne on the expanded or thickened end of the flower-stalk: this SPS end is the torus. In Fig. 187 all the ya Pease eee parts are seen as attached to the torus. fe ho nection chase This part is sometimes called recep- the single compartment. tacle, but this word is a common- language term of several meanings, whereas torus has no ( C (Fig. 189) in whieh the petals are borne © on the calyx-tube. af 953. ESSENTIAL ORGANS.—The essential 191. Simple pistils of buttereu p, one in organs are of two series. They are also longitudinal section, 189. Flower of fuchsia in section, other meaning. Sometimes one part is at- tached to another part, as in the fuchsia homologous with leaves. The outer series is composed of the stamens. The inner series is composed of the pistils. 124 THE PARTS OF THE FLOWER 254. Stamens bear the pollen, which is made up of grains or spores, each spore usually being a single plant cell. The stamen is of two parts, as readily seen in Figs. 187, 188, 189,— the enlarged terminal part or anther, and the stalk or filament. The filament is often so short as to seem to be absent, and the anther is then said to be sessile. The anther bears the Pact Cote pollen spores. It is made up gue Se of two or four parts (known pels. as sporangia or spore-cases), which burst and discharge the pollen. When the pollen is shed, the stamen dies. 255. Pisitls bear 193. Knotweed, a very common but inconspicuous plant the seeds. The pis- along hard walks and roads. Two flowers, en- 5 Se ee au eo Ce eee part or compart- ment, or of many parts. The different units or parts of which it is composed are carpels. Each carpel is homo- logous with a leaf. Each earpel bears one or more seeds. A pistil of one carpel is simple; of two or more carpels, compound. Usually the structure of the pistil may be determined by cut- ting across the lower or seed- bearing part. Figs. LOO} 19 194. The structure of a plum blossom se. sepals; p. petals; sta. stamens; 192 explain. : nified. stigma is said to be receptive. The stigma may remain receptive for several hours or even days, depending on the kind of plant, the weather, and how soon pollen is received. When fertilization takes place, the stigma dies. Observe, also, how soon the petals wither after the stigma has received pollen. 263. POLLINATION.—The transfer of the pollen from an- ther to stigma is known as pollination. The pollen may fall of its own weight on the adjacent stigma, or it may be carried from flower to flower by wind, insects, or other agents. There may be self-pollination or cross-pollination. 264. Usually the pollen is discharged by the bursting of the anthers. The commonest method of discharge is through a slit on either side of the anther (Fig. 202). Sometimes it discharges through a pore at the apex, as in azalea (Fig. 204), rhododendron, huckleberry, winter- green. In some plants a part of the anther wall raises or falls as a lid, as in barberry (Fig. 205), blue cohosh, May apple. The opening of an anther (as also of a seed-pod) is known as dehiscence. When an anther or seed-pod opens it is said to dehisce. I 130 FERTILIZATION AND POLLINATION 265. Most flowers are so constructed as to increase the chances of cross-pollination. We have seen (261) that the stigma may have the power of selecting foreign pol- len. The commonest means of insuring cross- .@ pollination is the different times of maturing of = s stamens and pistils in the same flower. In most cases the stamens mature first : the flower is then proterandrous. When the pistils mature first the flower is proterogynous. (Aner, andr, is a Greek | root often used, in combinations, for 204. 205. stamen, and gyne for pistil.) The dif- Any, of Barberry ference in time of ripening may be an (P?oamme theron hour or two,-or it may be-a day. The “2s wetyie ripening of the stamens and pistils at different times is known as dichogamy, and flowers of such character are said to be dichogamous. There is little chance for dicho- gamous flowers to pollinate themselves. Many flowers are imperfectly dichogamous—some of the anthers mature simul- taneously with the pistils, so that there is chance for self- pollination in ease foreign pollen does not arrive. Even when the stigma re- ceives pollen from its own flower, eross-fertilization may result (261). The hollyhock is proterandrous. Fig. 206 shows a flower recently expanded. The center is occupied by the column of stamens. In Fig. 207, showing an older flower, the long styles are conspicuous. 206. Flower of hollyhock; proterandrous. POLLINATION vo 266. Some flowers have so developed as to prohibit self- pollination. Very irregular flowers are usually of this cate- © 207. Older flower of hollyhock. gory. Regular flow- ers usually depend on dichogamy and the selective power of the pistil to in- sure crossing. Flow- which irregular vided with nectar and ers are very and pro- strong perfume usually pollinated by Gaudy col- ors probably attract are insects. insects in many eases, but perfume appears to be a greater attraction. The insect visits the flower for the nectar (for the making of honey) and may unknowingly carry the pollen. Spurs and are nectaries, but in spurless flowers the nectar is usually seereted in the bottom of the flow which are polli- nated by insects are said to be entomophilous (“insect-loving”’). Fig. 208 shows a larkspur. The en- velopes are sepa- rated in Fig. 209. The long spur at once suggests in- sect pollination. project into this sacs in the flower er-cup. Flowers 200 208. Flower of larkspur. The spur is a sepal. spur, apparently se Envelopes of a larkspur There are five wide sepals, the upper There are four small petals. one being spurred Two hollow petals ‘rving to guide the 132 FERTILIZATION AND POLLINATION bee’s tongue. The two smaller petals, in front, are differ- ently colored and perhaps serve the bee in locating the nectary. The stamens ensheath the pistils PZ (Fig. 210). As the insect stands on the “23 flower and thrusts his head into its center, the envelopes are pushed downward and outward and the pistil and stamens come in contact with his abdomen. Since the flower is pro- terandrous, the pollen which the pistils receive We from the bee’s AA abdomen must 210. Stamens of lark- spur, aianounding COMMC- le Oml>seagIh= DOS THU: other flower. Note a somewhat similar ar- rangement in the toad-flax or butter-and-eggs (Fig. 211). 267. Many flowers are polli- nated by the wind. They are said \ to be anemophilous (“ wind- loving”). Such flowers produce great quantities of pollen, for much of itis wasted. They usu- ally have broad stigmas, which expose large surface to the wind. They are usually lacking in gaudy colors and in perfume. Grasses and pine trees are typi- cal examples of anemophilous 211. Toad-flax is an entomophilous plants. flower. 268. In many eases cross- pollination is insured because the stamens and pistils are in different flowers (diclinous, 257). When the staminate and _ pistillate POLLINATION $353 flowers are on the same plant, e. g., oak (Fig. 212), beech, chestnut, hazel, walnut, hickory, the plant is moncecious (in one house”). When they are on different plants (poplar and willow, Fig. 213), the plant is dicecious (“in two houses”). Mone- cious and dicecious plants may be pollinated by wind or insects, or other agents. They are usually wind-polli- nated, although willows are mA s 212. Staminate catkins of oak. The pistil- often, if not mostly, insect- lita Thecus aes Gat har Toate aces pollinated. The Indian corn ESSE PONY a ees (Fig. 214) is a moncecious plant. The staminate flowers are in a terminal panicle (tassel). The pistillate flow- ers are in a dense spike (ear), inclosed in a sheath or husk. Each “silk” is a style. Each pistillate flower pro- duces a kernel of corn. Sometimes a few pistillate flowers are borne in the tassel and a few staminate flowers on the tip of the ear. 269. Although most flowers yen, are of such character as to insure or increase the chances of cross-pollination, there are some which absolutely forbid crossing. These flowers are usually berne beneath or on the ground, and they lack 213. Catkins of a willow. A staminate 4 flower is shown at s,andapisti showy colors and perfumes. late flower at p. The staminate — py hea i : te ° and pistillate are on different I hey are know nh as cleis- plants. togamous flowers (meaning “hidden flowers”). The plant has normal showy flowers which may be insect-pollinated, and in addition is provided 134 FERTILIZATION AND POLLINATION with these degenerate flowers. Only a few plants bear cleistogamous flowers. Hog- peanut, common blue violet, frimged win- tergreen, and dalibarda are the best subjects in the northern states. Fig. 215 shows a cleistogamous flower of the hog- peanut at a. Above the true roots, slen- der rhizomes bear these flowers, which are provided with a calyx and a curving corolla which does not open. Inside are the stamens and pistils. The pupil must not confound the nodules on the roots of hog-peanut with the cleistogamous flow- ers: these nodules are concerned in the appropriation of food. Late in summer the cleistogamous flowers may be found just underneath the mould. They never rise above ground. The following sum- mer one may find a seedling plant with aM onda Some the remains of the old cleistogamous with Staminate flower still-adhering to the root.” Whe he ee oyent = hog-peanut is a common low twiner in borne in the ear. woods. It also bears racemes of small pea-like flowers. Cleistogamous flowers usually appear after the showy flowers have passed. They seem to insure a crop of seed by a method which expends little of the plant’s energy. See Fig. 216. REVIEW.— What is fer- tilization? Pollination ? Define eross- and self-pol- 215. Hog-peanut, showing a leaf, and a lination. Which gives the eleistogamous'’ flower at a. better results, and how? What is meant by the selective power of the pistil? Describe a receptive pistil. Exhibit one. By what agents is cross-pollination secured? Howis pollen discharged? What is meant REVIEW ON POLLINATION 35 by the word dehiscence? What do you understand by dichogamy? What is its office? How frequent is it? What areentomophilous flow- ers? Anemophilous? Exhibit or explain one of each. What is the usual significance of ir- regularity in flowers? Where is the nectar borne? What are moneecious and diecious plants? Cleistogamous flowers? _ Nore.—The means by which cross-pollination is insured are absorbing subjects of study. It is easy to give so much time and emphasis to the subject, however, that an inexperienced observer comes to feel that per- fect mechanical adaptation of means to end is universal in plants, whereas it is not. One is likely to lose or to overlook the sense of proportions and to form wrong judgments. In studying cross-pollina- 216. Common blse violet. The familiar tion, one is likely to look first flowers are shown, natural size. The corolla is spurred. Late in the season, for devices which prohibit the cleistogamous flowers are often borne . : ae Sali on the surface of the ground. SF ' Be ( phi g es en, RO tat I aN ase 5 Sst ei ie i no i + y “ i ee Tea it nS cen Ou \ 338. Section of leaf of Polytrichum commune, ture-conditions. The inner surface of the leaf is covered with thin, longitudinal ridges of delicate cells which contain chlorophyll. These are shown in cross-section in Fig. 338. All the other tissue of the leaf consists of thick-walled, corky cells which do not allow moisture to penetrate. When the air is moist the green leaves spread out, exposing the chlorophyll cells to the air, but in dry weather the mar- 190 STUDIES IN CRYPTOGAMS gins of the leaves roll inward, and the leaves fold closely against the stem, thus protecting the delicate assimilating tissue. The antheridia and archegonia of polytrichum are borne in groups at the ends of the branches on different plants (many mosses bear = ox Naat both organs on the same branch). They MON “Zz are surrounded by involucres of charac- teristic leaves termed perichetia or peri- chetal leaves. Multicellular hairs known as paraphyses are scattered among the 339. Section jeans a receptacle of archegonia and antheridia, The invo- Polytrichum commune, showing lucres with the organs borne within paraphyses and antheridia. them are called receptacles or, less ap- propriately, “moss flowers.” Asin marchantia, the organs are very minute and must be highly magnified to be studied. The antheridia are borne in broad cup-like receptacles on the antheridial plants (Fig. 339). They are much like the antheridia of marchantia, but they stand free among the para- physes and are not sunk in cavities. At maturity they burst and allow the sperm-cells or spermat- ozoids to escape. In polytrichum when the re- ceptacles have fulfilled their function the stem continues to grow from the center of the cup (Fig. 340, m). The archegonia are borne in other receptacles on different plants. They are like the archegonia of marchantiaexcept that they stand erect on the end of the branch. The sporogonium which develops from the fertilized egg is shown in Fig. 340, a, b. It consists of a long, brown stalk bearing the spore-case at its summit. The base of the stalk is embedded in the end of the moss stem by which it is nourished. The capsule is entirely inclosed by a hairy cap, the calyptra, b. The ealyptra is really the remnant of the archegonium, which, for a time, inereases in size to accommodate 340. Polytrichum commune; f, f. fertile plants, one on the left in fruit; m, antheridial plant. MOSSES—FERNS 191 and protect the young growing capsule. It is finally torn loose and carried up on the spore-case. The mouth of the capsule is closed by a circular lid, the operculum, having a conical projection at the center. The operculum soon drops, or it may be removed, displaying a fringe of sixty-four teeth guarding the mouth of the capsule. This ring of teeth is known as the peristome. In most mosses the teeth exhibit peculiar hygroscopic movements, i. e., when moist they bend outwards and upon drying curve in toward the mouth of the capsule. This motion, it will be seen, serves to disperse the spores gradually over a long period of time. Not the entire capsule is filled with spores. There are no elaters, but the center of the capsule is occupied by a columnar strand of tis- sue, the columella, which expands at the mouth into a thin, mem- branous disk, closing the entire mouth of the capsule except the narrow annular chink guarded by the teeth. In this moss the points of the teeth are attached to the margin 5 of the membrane, allowing the spores to sift out through the spaces between them. When the spores germinate they form a_ green, \ branched thread, the protonema. This gives rise directly to moss plants, which appear as little buds on the thread. When the moss plants have sent their little rhizoids into F the earth, the protonema dies, for it is no longer neces- sary for the support of the little plants. FERNS The adder’s tongue fern, Ophioglossum vulgatum, shown in Fig. 341, is one of a peculiar type of ferns be- longing to the family Ophioglossacew. This plant has a short, subterranean stem from which a single frond un- folds each year. The roots arise near the bases of the leaves. The leaves are curiously divided into a sterile and a fertile part, the latter being a sporophyll. The sterile part has a tongue-shaped blade which is narrowed OAL. to a petiole. The young leaves are inclosed by the Ophioglossum sheathing base of the petiole. The growth is very Ywlsstum, slow, so that it takes several years for each leaf to develop before it is ready to unfold, During its development each leaf is sheathed by the one preceding it. The sporophyll is elevated on a stalk arising near the base of the sterile part of the frond, The upper part consists of a spike bearing 192 STUDIES IN CRYPTOGAMS two rows of large spore-cases or sporangia sunk in the tissue. At maturity the sporangia open by transverse slits and discharge the inclosed spores. When the spores germinate they produce subterranean tuberous prothallia which, however, are rarely found, and of whose history little is known. They develop archegonia and antheridia beneath the surface of the ground, and the fertilized egg produces the young fern plant. The generations of the true ferns are explained in Chapter XXIV. EQUISETUMS, OR HORSETAILS There are about twenty-five species of equisetum, constituting the only genus of the unique family Equisetacew. Among these E. arvense is common on clayey and sandy soils. In this species the work of nutrition and that of spore-production are performed by separate shoots from an underground rhizome. The fertile branches appear early in spring. The stem, which is 3 to 6 inches high, consists of a number of cylindrical, furrowed internodes each sheathed at the base by a circle of scale-leaves. The shoots are of a pale yellow color. They contain no chlorophyll, and are nour- ished by the food stored in the rhizome (Fig. 342). The spores are formed on specially developed fertile leaves or sporophylls which are collected into a spike or cone at the end of the stalk (Fig. 342, a). A single sporophyll is shown at b. It consists of a short stalk expanded into a broad, mushroom-like head. Several large sporangia are borne on its under side. The spores formed in the sporangia are very interesting and beau- tiful objects when examined under the microscope (XX about 200). They are spherical, green bodies each surrounded by two spiral bands attached to the spore at their intersection, s. These bands exhibit hygroscopic movements by means of which the spores become entan- gled, and are held together. This is of advantage to the plant, as we shall see. All the spores are alike, but some of the prothallia are better nourished and grow to a greater size than the others. The large pro- thallia produce only archegonia while the smaller ones produce antheridia. Both of these organs are much like those of the ferns, and fertilization is accomplished in the same way. Since the pro- thallia are usually dicecious the special advantage of the spiral bands holding the spores together so that both kinds of prothallia may be in EQUISETUMS—ISOETES 193 close proximity, will be easily understood. As in the fern, the fertil- ized egg-cell develops into an equisetum plant. The sterile shoots, Fig. 342, sf, appear much later in the season. They give rise to repeated whorls of angular or furrowed branches. The leaves are very much reduced scales, situated at the internodes. The stems are provided with chlorophyll and act as assimilating 342. Equisetum arvense; st, sterile shoot; f, fertile shoot showing the spike at a; b, sporophyll, with sporangia; 8, spore. tissue, nourishing the rhizome and the fertile shoots. Nutriment is also stored in special tubers developed on the rhizome. Other species of equisetum have only one kind of shoot—a tall, hard, leafless, green shoot with the spike at its summit. Equisetum stems are full of silex and they are sometimes used for scouring floors and utensils: hence the common name “ scouring rush.” ISORTES Isoétes or quillworts are usually found in water or damp soil on the edges of ponds and lakes. The general habit of a plant is seen in Fig. 343, a. It consists of a short, perennial stem bearing numer- ous erect, quill-like leaves with broad sheathing bases, The plants are commonly mistaken for young grasses. M 194 STUDIES IN CRYPTOGAMS Isoétes bears two kinds of spores, large roughened ones, the macrospores, and small ones or microspores. Both kinds are formed in spor angia borne in an excavation in the expanded base of the leaf. The macrospores are formed on the outer, and the microspores on the inner leaves. A sporangium in the base of a leaf is shown at b. It is partially covered by a thin membrane, the velum. The mi- nutetriangular appendage at the upper end of the sporangium is ealled the ligule. The spores are liberated by the decay of the sporangia. They form rudimentary prothallia of two kinds. The microspores produce prothallia with antheridia, while the macrospores produce prothallia with archegonia. Fertilization takes place as in the mosses or liverworts, and the fer- tilized egg-cell, by continued growth, gives rise again to the isoétes plant. ALTERNATION OF GENERATIONS In Chapter XXIV the alternation of generations and the terms gametophyte and sporophyte were explained. In many of the plants just studied, this alternation is more clearly and beautifully marked than in any other groups of plants. In B49). [goates valowinigh Habitmes each generation, the reproductive body plant at a; b, base of leaf (egg or spore) gives rise to a new plant- showing sporangium, vel- form or generation different from the um, and ligule. parent generation. In the liverworts the thallus produces the egg. The fertilized egg-cell is the beginning of anew plant, but this new plant is not like the thallus which produced the egg, nor does it lead an independent existence. It is the sporo- gonium, which, although it is attached to the thallus, is not a mor- phological part thereof. The sporogonium produces spores. It is the sporophyte generation of the plant, and not until the spores germinate is the thallus again produced. The same is true in the mosses. The “moss plant” produces the egg-cells. It is the gametophyte. The fertilized egg-cell develops into the sporophyte—the spore-case and its stem. We can pull the stem of the capsule out of the moss plant and thus separate the sporophyte from the gametophyte. ALTERNATION OF GENERATIONS 195 The fungi and algzw are omitted from these remarks. In the former there is nothing analogous to the sporophyte and the gameto- phyte. In alge like spirogyra, evidently the whole plant is a ga- metophyte and, since the zygospore germinates directly “into a new gametophyte, there is probably no sporophyte. In some other alge traces of a sporophyte have been found, but the discussion of these would lead too far for the present purpose. In the ferns the egg-cells are developed on the prothallus. This then is the gametophyte. It corresponds to the thallus of mar- chantia and to the “moss plant,” but it has become much reduced. The plant developing from the fertilized egg-cell is the large and beautiful “fern plant” differentiated into stems and leaves. Since the fern plant produces the spores directly, it is the sporophyte and corresponds to the shaft and capsule of the mosses. Both sporophyte and gametophyte lead an independent existence. As we pass on to equisetum and isoétes, the sporophyte is still more conspicuous in comparison with the gametophyte. In isoétes the prothallus (gametophyte) is very rudimentary, consisting only of a few cells remaining within the spore, which merely bursts to expose the archegonia or to allow the sperm-cells to escape. Moreover, the spores have become differentiated into micro- and macrospores corre- sponding to the pollen and embryo-sae of higher plants. This gradual increase of the sporophyte and reduction of the gametophyte can be traced on through the flowering plants in which “the plant” is the sporophyte, and the gametophyte is represented simply by a few cells in the germinating pollen grain, and in the embryo-sae. One of the tuft-mosses (Leucobryum) Outside and inside views of a tuft, the latter showing the radiating stems extending to the light 344. Desert vegetation. ucti grow only in special regions. Arizona. ‘ The tree @ of the Hudson. ides d Palis row. first opportunity to g ize the ants se li 15, P 9 Vv PART II—THE PLANT IN ITS ENVIRONMENT CHAPTER XXVI WHERE PLANTS GROW 326. ENVIRONMENT.—The circumstances and surround- ings in which an organism lives constitute its environ- ment. The environment comprises effects of sail, mois- ture, temperature, altitude, sunlight, competition with animals and other plants, and the like. An organism is greatly influenced by the environment or conditions in which it lives. Not only must a plant live and grow and multiply its kind, but it must adapt itself to its environ- ment. 327. The particular place in which a plant grows is known as its habitat (i. e., its “habitation”). The habi- tat of a given plant may be a swamp, hill, rock, sand plain, forest, shore. The plant inhabitants of any region are known collectively as its flora. Thus we speak of the flora of a meadow or a hill or a swamp, or of a country. The word is also used for a book describing the plants of a region (as in Part IV). 328. PLANTS GROW WHERE THEY MUST.—The plant is not able to choose its environment. It has no volition. Its seeds are scattered: only a few of them fall in pleas- ant places. The seeds make an effort to grow even though the places are not favorable; and so it happens (197) 198 WHERE PLANTS GROW that plants are often found in places which are little adapted to them. See the fern growing on a brick in Fig. 69. Plants must grow in unoccupied places. 329. Not only do the seeds fall in unfavorable places, but most places are already occupied. So it comes that plants grow where they must, not where they will. There are, of course, certain limits beyond which plants cannot grow. Water lilies can thrive only in water, and white oaks only on dry land, but it is seldom that either the water lily or the oak finds the most congenial place in which to grow. Fine large plants of the lily and strong giant trees of the oak are so infrequent, as compared with the whole number, that we stop to admire them. 330. Originally, plants were aquatic, as animals were. Much of the earth was sea. Many plants are now aquatic, and the larger number of these—as alge and their kin— belong to the lower or older forms of plant life. Many plants of higher organization, however, as the water lilies, have taken to aquatie life. True aquatie plants are those which always live in water, and which die when the water dries up. They are to be distinguished from those which live on shores or in swamps. Aquatic plants may be wholly dmmersed or under water, or partly emersed or standing above the water. Most flowering aquatic plants come to the surface to expand their flowers or to ripen their fruits. Some aquatie plants are free-swimming, or not attached to the bottom. Of this kind are some utric- 316. The lichen grows on the hard rock. ’ AQUATIC AND TERRESTRIAL PLANTS 199 ularias, or bladder-worts. In some waters, particularly in the ocean, there are enormous quantities of free-swim- ming microscopic life, both animal and vegetable, which is carried about by eurrents: this is known under the general name of plankton (Greek for “wandering” or “roaming ”’). 331. The general tendency has been for plants to become terrestrial, or land-inhabiting. Terrestrial plants > ° 347. Sphagnum bog, green and living on top, but dead and dying nnderneath Sphagnum moss is used by nurserymen and florists as packing material for plants. often grow in wet places, but never in water throughout their entire life; of such are swamp, bog, and marsh plants. Some plants have the ability to grow in standing water when young and to become terrestrial as the water dries up. Such are amphibious. Some buttercups are examples. 332. Some plants grow in very special soils or special localities, and consequently are infrequent or are confined to certain well-marked geographical regions. Fig. 344, Common plants are those which are able to accommodate 200 WHERE PLANTS GROW themselves to widely different environments. Weeds are ex- amples. Many plants have become so specialized in habitat as to be parasitic, saprophytic, or epiphytic. Chap. XIII. 333. Common plants often grow in most unusual and difficult places. Note that some weeds grow not only in fields, but often gain a foothold in chinks in logs, on rotting posts, in crotches of trees, on old straw stacks, in clefts and crannies of rocks. In moist climates, as Eng- land, plants often grow on thatched roofs. 334. Plants may be said to be seeking new places in which to grow. Whenever ground is cleared of vegeta- tion, plants again spring up. The farmer plows the meadow or pasture, and immediately a horde of weeds appears. Any breach or break in the earth’s surface makes room for a new group of plants. Note how the ‘allway embankments and the newly graded roadsides take on a covering of vegetation. Observe the ragweed. When- ever soil is formed at the base of a cliff, plants at once secure a foothold. Fig. 345. 335. PLANTS AID IN THE FORMATION OF SOIL. — This they do in two ways: by breaking down the rock; by passing into earth when they decay. Even on the hardest rocks, lichens and mosses will grow. Fig. 346. The rhizoids eat away the rock. A little soil is formed. Ferns and other plants gain a foothold. The crevices are entered and widened. Slowly the root acids corrode the stone. Leaves and stems collect on the rock and deeay. Water and frost lend their aid. As the centuries pass, the rock is eaten away and pulverized. Note the soil which collects on level rocks in woods where wind and rain do not remove the accumulations. 336. In bogs and marshes and on prairies the remains of plants form a deep black soil. In bogs the vegetable matter is partially preserved by the water, and it slowly becomes solidified into a partially decayed mass known as 348. A landscape devoid of vegetation. Western United States. O49. A landscape with vegetation Belgium 202 WHERE PLANTS GROW peat. When dug out and dried, peat may be used as fuel. Finally it may decay and make a vegetable soil known as muck. When thoroughly decayed, plants become vege- table mold or humus. New plants grow on peat or muck, and the accumulations year by year tend to raise the level of the bog, and the surface may finally become so high as to support plants of the high lands. The chief agent in the formation of peat bogs is sphagnum moss. New moss grows on the old, and the bog becomes higher as time goes on. Fig. 347. 337. PLANTS CONTRIBUTE TO SCENERY. — Aside from sky and air, natural scenery depends chiefly on two things: the physical contour of the earth; the character of the vegetation. Attractive landscapes have a varied vegeta- tion. Imagine any landseape with which you are familiar to be devoid of plants. Compare Figs. 348 and 349. REVIEW.— What is meant by environment? By habitat? Flora? What determines where plants shall grow? What is an aquatie plant? Explain immersed, emersed, free-swimming. Whatis plankton? Ex- plain terrestrial. Amphibious. Why are some plants rare or local? Why are some plants common? Name some unusual places in which you have seen plants growing. Give examples of how plants occupy the new places. Howdo plants aid in the formation of soil? Explain what is meant by peat, muck, humus. How are peat bogs formed ? What relation have plants to scenery ? The same landscape 1n winter and summer. CHAPTER XXVII CONTENTION WITH PHYSICAL ENVIRONMENT 338. THE PHYSICAL ENVIRONMENT.— We have seen (326) that the environment in which a plant grows is made up of two sets of factors—the physical environ- ment of climate and soil, and the organic environment of competing animals and plants. 339. ADAPTATION TO CLIMATE IN GENERAL. — Every particular climate causes particular modifications in its plants. There are two general ways, however, in which plants are modified or adapted to climate: modification in the length of the period of growth; modification in stature. Any modification of the plant, visible or invis- ible, which adapts it to grow in a climate at first inju- rious to it, is acclimatization. 340. In short-season climates, plants hasten their growth. They mature quickly. Indian corn may re- quire five or six months in which to mature in warm countries, but only three months in very cold countries. Nearly all garden vegeta- bles mature quicker from the time of planting in the 5 W ANY, ft} when they are raised from —™ ——— North than in the South seeds grown in their respec- $50. Germination of corn grown in Heniitestion, “Geeaemien are eee aware of this and they like to raise seeds of early varieties in the North, for such seeds usually give “early” plants. Many plants which are perennials in warm countries be- come annuals or plur-annuals in cold countries(14). (203 ) 204 PHYSICAL ENVIRONMENT 341. Even germination is usually more rapid from northern-grown seeds than from southern-grown seeds of the same kind. The plants “come up” quicker. Se- cure seeds of the same variety of corn or bean grown in the Gulf states and in the northern states or Canada and make the experiment (Fig. 350). The same results often show in the vegetation of cuttings of trees and grape vines from the South and North. Vege- tation is quick in the North: the “burst of spring” is usu- ally more rapid. 342. Plants are usually dwarf or smal- ler in stature in short-season eli- 351. Evergreen trees on wind-swept heights of the mates Indian Rocky Mountains. corn is a con- spicuous example. As one ascends high mountains or travels in high latitudes, he finds the trees becoming smal- ler and smaller, until finally he passes beyond the regions in which the trees can -grow. Many of the HEsquimaux doubt the statements of travelers that there are plants as high as a man. In these high altitudes and high latitudes, plants tend also to become prostrate. 343. PLANTS ARE INFLUENCED BY WIND.—In regions of strong prevailing winds, as on lake and sea shores and on hills and mountains, tree-tops develop unsymmetrically holl One-sided 206 PHYSICAL ENVIRONMENT and are heaviest on the leeward side. Figs. 351, 352. Ob- serve this fact in orchards in windy regions, and note that the most unsymmetrical trees are those on the exposed side of the plantation. ‘ ve 344. Trees often lean away from the prevailing winds. . Fig: 353. The tips of the branches of ex- posed trees usually indicate whether there are strong prevailing winds. Fig. 854. Observe trees in pastures and along road- sides, particularly in high places and within a few miles of exposed shores. Note the tip-top spray of hemlock trees. 345. PLANTS ARE PROFOUNDLY INFLUENCED BY SOIL.— The food supply varies with the kind of soil; and the food supply determines to a large extent the character of the individual plant. On poor soils plants are small; on rich soils they are large. The difference between poor and good yields of wheat, or any other erop, is largely ¢ question of soil. The farmer reinforces his poor soils by the addition of fertilizers, in order to make his plants vary into larger or more productive individuals. 346. The moisture-content of the soil exerts a marked influence on plants. We have found (154) that a large 304. A tree which shows which way the wind blows. Oklahoma. PLANTS ARE INFLUENCED BY SOIL 207 part of the plant-substance is water. The water is not only itself plant-food, but it carries other foods into the plant and transports them from tissue to tissue. However rich a soil may be in mineral plant-foods, it is inert if it contains no moisture. The character of the plant is often determined more by the moisture in the soil than by all the other food materials, Note how rank the plants are in low places. Observe how the weeds grow about the barn where EOE 355. “Lodged” oats. On rich ground the grain is often broken by wind and rain, the plants having grown so heavy asto be unable to support themselves, the soil is not only rich but where moisture is distributed from the eaves. Contrast with these instances the puny plants whieh grow in dry places. In dry countries irriga- tion is employed to make plants grow vigorously. — In moist and rich soil plants may grow so fast and so tall as not to be able to withstand the wind, as in Fig, 355. 347. PLANTS ARE INFLUENCED BY THE EXPOSURE OF THE PLACE IN WHICH THEY GROW.—The particular site or out- look is known as the exposure or aspect. The exposure, for instance, may be southward, eastward, bleak, warm, 208 PHYSICAL ENVIRONMENT eold. plants these plants he ealls weeds. Determine how much room anapple tree, or other plant, occupies: then ecaleulate how much space would be required for all the seed- lings of that tree or plant. The greater the population of any area, the less chances have other plants to gain a foothold. When the wheat completely covers the ground, as in Fig. 357, there are no weeds to be seen. 352. Plants of different : “i 360, The clematl limbing into the sunlight form and habit may grow Compare Fig. 73. on the forest floor. aunts “ | = i 0 61. Low shade- 3 forest. imeval pine 362. A pr g the roadway for ichigan. ale in as come gn vegetation h el DIVERGENCE OF CHARACTER 215 together, and thereby the area may support more plants than would be possible if only one kind were growing on it. This principle has been called by Darwin the divergence of character. When an area is occupied by one kind of 363. On the top of an evergreen forest plant, another kind may grow between or beneath, Only rarely do plants of close botanical relationship grow to- gether in compact communities. A field which is full of corn may grow pumpkins between. Fig. 3858. the stem of the cucumbér. a Bordered pits, when the pits are in- mall A closed in the cell-wall, as in wood of ©) ee pines and other conifers. Fig. 388. sss. Bordered pits in Spiral, with the thickening in a spiral pine wood. band, as in the primary wood of most woody plants and in the veins of leaves. Fig. 389. Annular, with thickening in the form of rings; seen in the large vessels of the bundles in stem of Indian corn. Fig. 389. Scalariform, with elongated thin places in the wall, alternating with the thick ridges which appear like the rounds of a ladder. Fig. 389. These are well shown in a longitudinal section of the root of the brake fern (Pteris). 391. MULTIPLICATION OF CELLS.—Cells give rise to new cells. Thus does the plant grow. The most com- mon method by which cells are multiplied is that called cell division. A modified form of cell an so division is called budding. Cell di- [& vision is a process by which two (or more) cells are made from one original cell. Cells which have an a abundance of protoplasm are usually l},, 380. Markings in cell-walls Phe sp, spiral; an, annular; process is at first an internal one, — s, sealwriform, most active in cell division, The nueleus gradually divides into two masses and the protoplasm of the cell is apportioned between these two nuclei; a new. cell-membrane, or partition wall, is usually thrown across and the cell is completely 238 THE CELL divided into two cells. Fig. 390. In some eases, however, the nucleus divides many times without the formation of a cell-wall. The cell which began to divide is called the mother cell, and the resulting cells are daughter cells. 392. Cell bud- ding is a variety of cell division in which the cell is not di- vided in the mid- dle. The mother cell pushes out a 390. Four steps in process of cell-division. 3 Mother cell at left, far advanced in division; daughter protuberance, which BUS ED SE becomes separated by a constriction of the walls. Cells of the yeast plant and the spores of many fungi multiply in this way. 393. In no ease, so far as we yet know, can the cell divide without a division of the nucleus and the protoplas- mic mass. There are two methods of nuclear division: (1) direct, as found in the old cells of nitella, tradescantia, and others, in which the mass of the nucleus divides by simple constriction; (2) indirect, as found in all actively growing tissue, in pollen grains, spores, ete. There are several stages in the latter process. The nucleus divides in intri- cate methods, giving rise to odd forms known as nuclear figures. Mitosis and karyokinesis are names sometimes given to indirect nuclear division. The study of this pro- cess is a very difficult one, as it requires a very high power microscope to see the different stages. They are easily seen in cells found in buds of convallaria and in pollen grains of that plant, but may be studied in all plants. The process is too difficult for the beginner to trace, but it is outlined in the note on next page. Fig. 390 is not intended to represent all the stages in indirect nuclear division. ReEview.— What are some of the forms of cells? Name the parts of a living cell. What part or parts are essential in all cases? Give KARYOKINESIS 239 your idea of the nature of protoplasm. What differences did you find between the cells of yeast and those of green alga? In what ways do they resemble each other? Tell the same of cells of protococcus and of apple, or of other material studied. What is a vacuole? What does it usually contain? Name two kinds of movements of protoplasm within the cell-wall, and explain how each may be observed. . Name and describe two movements of naked protoplasm. Tell something of the texture of cell-walls. What causes the markings found on cell- walls? Name five types of markings. Draw two figures to show structure of bordered pits. Make a sketch of spiral, annular, and sealariform markings. Name two methods of cell-multiplication. Describe the process of cell-division. How does cell-budding differ from cell-division? Name two methods of nuclear division. Which is the more common method ? Nore TO PARAGRAPA 393.—Karyokinesis (the indirect or mitotic process of nuclear division) is an intricate subject. The details vary in different plants, but the essential stages are as follows: During the resting stage the nucleus is surrounded by a very deli- cate but distinct membrane. Within this inclosure is an intricate net- work of colorless (linin ) threads bearing very numerous granules, which in stained preparations are highly colored, and for this reason have received the name chromatin. The network is surrounded by nuclear- sap, and often incloses within its meshes a large body called the nucleolus. As the time for division approaches the chromatin network changes into a definite, much-coiled, deeply stained ribbon, in which the granular structure is much less noticeable, and this in turn seg- ments transversely into a number of parts called chromosomes, The pretoplasmie fibrils immediately surrounding the nucleus now grad- ually converge towards two points lying on opposite sides of the nucleus and at a slight distance from the membrane. This is accom- plished in such a way that a spindle of nearly colorless threads is produced, with the two previously mentioned points of convergence acting as poles. Meanwhile both the nuclear membrane and the nu- cleolus have disappeared, but whether these structures take part in the formation of the spindle is yet an open question. Radiations of protoplasmie threads called asfers sometimes occur around the poles, and in a few lower plants, as well as in most animals, the pole is occupied by a small spherical body termed a centrosphere, The steps so far are known as the prophase stages, The chromosomes now move to the equator of the spindle, where they arrange themselves in a definite manner, forming the so-called nuclear-plate (metaphase stage). Each segment splits longitudinally, apparently on account of 240 THE CELL the contractive action of the spindle fiber to which it is attached; and one daughter-segment passes to each pole (anaphase stage). Each of the two groups of daughter-segments very soon becomes surrounded by a new membrane, the chromosomes gradually fuse end to end, the nucleolus reappears, and at length two resting nuclei are produced similar in every respect to the parent nucleus (telophase stage). Meanwhile each spindle fiber becomes swollen at the equator, thus producing a series of dots all arranged in one plane. These at length fuse, forming a delicate transverse cell-membrane, which by the pe- ripheral expansion of the spindle at length reaches the lateral walls, and cell-division is thus complete. This process of indirect nuclear division is one of the most wonderful phenomena yet discovered in organic development, not only on account of its intricacy and beauty, but also because it has been found that hereditary characteristies are in all probability transmitted solely through the chromosomes. The longitudinal division and separation seem to be for the purpose of insuring equal apportionment of the hereditary substance to each daughter-nuecleus. The subject, however, is still in its infaney, and authors disagree both as to details and as to theoretical considerations. NoTe ON Score, APPARATUS, AND METHODS.—The work outlined in Part III is sufficient, if well done, to occupy one period of the pupil’s time each school day for six weeks. These chapters are intended only as laboratory guides. The pupil should work out each structure or part for himself before taking up the succeeding subject. The work in this Part deals with only the elements of the subject, but it is as much as the high school pupil ean hope to take up with profit. Apparatus.—The apparatus necessary for the work outlined in these chapters on histology may be obtained from dealers in micro- scopes and laboratory supplies at a low figure. Schools should obtain catalogues from the following and other reliable dealers: Bausch & Lomb Optical Co., Rochester, N. Y. Eimer & Amend, New York. The Franklin Edueational Co., Boston. Queen & Co., Philadelphia. Richards & Co., Chicago and New York. Speneer Lens Co., Buffalo. Williams, Brown & Earle, Philadelphia. Geneva Optical Co., Chicago. Whitall, Tatum & Co., New York. Chas. Lentz & Sons, Philadelphia. Richard Kny & Co., New York. Cambridge Botanical Supply Co., Cambridge, Mass. APPARATUS AND METHODS 241 The microscope should have a one-inch and perhaps a two-inch eye-piece and two objectives of say $- and }-inch focal lengths. By arranging the laboratory study of the pupils at different times each microscope may be used by three, four, or even more pupils. There should be a microtome or section-cutter for use by the class. Each pupil should have his own individual tools and bottles of reagents, as follows: 1 good razor (hollow-ground on one side only), 1 small sealpel, 1 pair forceps, 2 sharp needles mounted in handles (as penholders) (Fig. 199), 1 medicine dropper, 1 small camel’s hair brush, A number of slides and cover-glasses. Of reagents, stains, and other chemicals, there should be the following: Glycerine, Ninety-five per cent alcohol, Formalin (40 per cent formaldehyde ). Clearer (made of three parts turpentine and two parts melted crystals of carbolie acid), Canada balsam, Ether, 2 per cent and 5 per cent collodion, Iodine dissolved in water, ie he ‘* aleohol, Hematoxylin, Copper sulfate solution, Potassium hydroxide solution, Fehling’s solution (see paragraph 397), Aleanin (henna root in alcohol). The two per cent collodion is made of forty-nine parts aleohol, forty-nine parts ether, two parts soluble cotton. This strength is suitable to use in sticking sections to the glass slide to prevent their escape during the staining and clearing process. It need not be used unless desired. Collodion is often useful for imbedding material, as indicated under the head “Imbedding” on page 245, Pupils must exereise great care in using carbolie acid, as it burns the flesh. Hematoxylin stain may be obtained of dealers in a condition 1c 242 THE CELL ready for use, or may be prepared by this recipe (Gage’s Hematoxry- lin): Distilled water 200 ec. and potash alum 73 grams, boil together for five minutes in glass dish or agate ware. Add enough boiled water to bring the volume back to 200 ce. When cool add 4 grams of chloral hydrate and > gram of hematoxylin erystals which have been dissolved in 20 ce. of ninety-five per cent alcohol. This is quite permanent, and becomes of a deeper color after standing for some time if left in a light place and frequently shaken. It stains the tissues which bear protoplasm and cellulose walls, causing them to stand out in contrast with the other tissues. Preparing and Keeping Laboratory Material.—In preparing material for the experiments outlined in Part III., the pupil or teacher will find it best to get much of the material during the growing season and preserve it until the time for use. Soft material should be dehydrated and hardened by placing it in about 40 per cent alcohol for several hours to two days, according to its size, and then plac- ing it in about 70 per cent for the same length of time. It can then be placed in 80 per cent alcohol, and is ready for use at any time. When thus preserved, the tissues containing protoplasm are some- times much shrunken. For this reason it is well to preserve some of the material in a liquid containing a great deal of water. One of the best liquids is a 2 per cent or 244 per cent solution of formalin. This preserves material well but does not dehydrate it. Formalin burns the flesh. Free-hand Cutting and Mounting.—To eut sections, the material may often be held between pieces of pith or smooth cork in the microtome or fingers. The material and sections should be kept wet with aleohol during the time of cutting. The sections when cut should be wet in water, then stained with hematoxylin for a few minutes; drain off the hematoxylin and rinse with water; then use ninety-five per cent alcohol to extract all the water from the sections; then pour on clearer for a few minutes. Put a drop of Canada balsam on the sections, and they are ready for the thin cover glass. Monnts thus made are permanent. Some reasons for the steps in the process may be understood from the fact that hematoxylin does not mix readily with alcohol, and balsam does not mix with water nor with alcohol. Sections mounted before: (ter *‘TOyoo[e 10; ouUO puR 1 55 cl Lae 8 THE KINDS OF PLANTS NUMBER OF PLANTS.—Above 125,000 distinet kinds or species of seed-bearing plants are known and described. Probably little more than one-half of the total number now existing on the earth are known. Even in the older coun- tries and regions, seed-bearing plants heretofore unknown to science are discovered now and then. Outlying regions are relatively little known botanically. The larger part of Africa, South America, Central Ameriea, China, Cen- tral Asia, and the tropical islands are only imperfectly explored for plants. Cryptogamous plants are far more numerous in kinds than seed-plants, and many kinds—as, for example, various bacteria—are almost infinite in numbers of individuals. In the lower ranges of eryptog- amous plants, as in fungi and bacteria, many new kinds are constantly being described even in countries in which they have been most carefully studied. SPECIES.—Each kind of plant is called a species, There is no absolute mark or characteristic of a species. Between many kinds there are intermediate forms, and some kinds vary immensely under different conditions. What one botanist considers as a distinct species, another botanist may regard as only a variety or form of another species. No two botanists agree as to the number of species in any region. Species are not things in them- selves. In practice, any kind of plant which is distinet enough to be recognized by a description, and which is fairly constant over a considerable territory, is called a (275) MAG) THE KINDS OF PLANTS species. We make species merely to enable us to talk and to write about plants: we must have names to eall them by. The different kinds of plants are the results of evolution. Probably none of them were created in the beginning as we now find them. NAMES OF SPECIES.—For one hundred and fifty years (since Linneeus published his “ Species Plantarum” in 1753), species have been known by two names, the generic and the specific. The generic name is the name of the genus or group to which the plant belongs: it corresponds to a surname. The specific name belongs only to the particular species or kind: it corresponds to a given or Christian name. Both names are necessary, however, to designate the species. Thus Quercus is the generic name of all the oaks. Quercus alba is one of the oaks (the white oak), Q. virens (the live oak) another. All maples belong to the genus Acer, and all elders to Sambucus. The same specific name may be used in any genus, as the same Christian name may be used in any family. Thus, there is a Quercus nigra, Sambucus nigra, Acer nigrum, “niger” meaning black. By common consent, the oldest proper name of any species must stand. If a species happens to have been named and described twice, for example, the first name, if in the proper genus, must hold; the later name becomes a synonym. It sometimes happens that the same specific name has been given to different plants of the same genus. Of course this name can be allowed to stand for only one species, and the other species must receive another name. In order to avoid confusion of this and other kinds, it is customary to write the author’s name with the species- name which he makes. Thus, if Gray describes a new Anemone, his name is written after the plant name: 6 clas eiers'ele eo ACCC EAGAL a een AA ae 1. Daucus AA, Fruits not bristly. B. Carpels or “seeds” winged............. BOCES ree Pastinaca BB. Carpels wingless. c. Axis from which the carpels separate not splitting in TWO... ss sc00 sla eimrates ate o viene swespesviedss cues pasvucds A DUUM co. Axis splitting in two when the carpels or “seeds” fall. 4. Carum 1. DAUCUS. Carxor. Annuals or biennials, bristly, slender and branching, with small white flowers in compound umbels, the rays of which become inflexed in fruit; the fruit oblong, ribbed and bristly. D, Cardta, Linn. Carrot. Fig. 180. Leaves pinnately decompound, the ultimate segments lanceolate: outer flowers with larger petals. Europe; cultivated for the root, and extensively run wild. 2. PASTINACA. Paxsnip. Tall, smooth biennials of strict habit and with pinnately compound leaves: flowers yellow, in compound umbels with scarcely any involucres: fruit oval, very thin, wing-margined., P. sativa, Linn. Parsnip. Flowering stem 2-4 ft. tall, grooved, hol low: leaflets ovate or oblong, sharp-toothed. Europe; cultivated for its roots and also run wild. 3. APIUM. Crery, Annuals or biennials, with large pinnate leaves: flowers white, in small umbels: fruit small, usually as broad as long, each carpel S-ribbed: axis from which the carpels fall not splitting in two, 326 THE KINDS OF PLANTS A. gravéolens, Linn. Celery. Biennial, smooth: leaflets 3-7, wedge- shaped or obovate, the lower ones about 3-divided, round-toothed. Europe; cultivated for its petioles, which have become greatly enlarged. 4. CARUM. Caraway. Slender and erect, smooth annual and biennial herbs with pinnate leaves: flowers white or yellowish, in compound umbels provided with in- volucres: axis bearing the carpels splitting in two at maturity. CG. Carui, Linn. Caraway. Stem furrowed, 1-2 ft.: leaves cut into thread-like divisions: flowers white. Europe. Cultivated for its fruits, known as “Caraway seed,” and also run wild. C. Petroselinum, Benth. Parsley. One to 3 ft.: leaflets ovate and 3-cleft, often much cut or “curled” in the garden kinds: flowers yellowish. Europe. cc. GAMOPETALA. XX. LABIATA. Minr Famity. Herbs, usually of aromatic scent, with 4-cornered stems and opposite usually simple leaves: flowers typically 2-lipped: stamens 4 in 2 pairs, or only 2: ovary deeply 4-lobed, forming 4 indehiscent nutlets in fruit. A well-marked family of some 2,700 species, dis- tributed in about 150 genera, of both temperate and tropical regions. To this family belong the various mints, as peppermint, spearmint, catnip, hyssop, thyme, pennyroyal, savory, rosemary, sage, hore- hound, balm, basil. Flowers mostly in whorls in the axils of leaves or bracts, sometimes forming interrupted spikes. A. Stamens 2. B. Calyx about equally toothed, hairy within ............. 1. Monarda BIE (ObIiyps Baliye) devel ENR! \iaqN ON 666 oo0 Goooa noo oondoDsedos 2. Salvia AA. Stamens 4. B. Corollarscarcelys2-lippedcenmer- =e ee le tlt eC TILIORe BB. Corolla strongly 2-lipped. Cie A© silty ex (2 UD COS pepe ote oka < eeliol oetfereteleVora clo rstiena abel (ol stra baat p-tai 4. Brunella cc. Calyx nearly or quite regular. bp. Upper or inner pair of stamens longer............5. Wepeta pp. Lower or outer pair longer. E. Tube of corolla including the stamens.........6. Marrubium EE. Tube with stamens projecting ................. 7. Leonurus 1. MONARDA. Hoxrse-minv. Rather stout, mostly perennials, with flowers in close terminal heads: ealyx tubular, 15-nerved, hairy in the throat, the teeth nearly equal: corolla strongly 2-lipped, the upper lip erect, the lower spreading and 3-lobed. LABIAT® B27. M. fistulosa, Linn. Two to 5 ft., in clumps: leaves ovate-lanceolate: flowers in a clover-like flattish head: calyx slightly curved: corolla about 1 in. long, purple. Common in dry places. 2. SALVIA. Sace. Annuals or perennials, mostly with large and showy flowers: calyx and corolla 2-lipped: upper lip of corolla large and usually arched, entire or nearly so, the lower lip spreading and 3-lobed: stamens 2, short, the anther locules separated by a transverse bar. S. officinalis, Linn. Common sage. Erect low perennial, with gray pubescent foliage: leaves oblong-lanceolate, crenulate, very veiny: flowers blue, in spiked whorls. Europe; used for seasoning. S. spléndens, Sell. (S. coccinea of gardens). Scarlet sage. Tender perennial from Brazil, but much cultivated for its bright scarlet floral leaves, calyx, and corolla: leaves ovate-pointed. 3. MENTHA. Mint. Low perennials: calyx with 5 similar teeth: corolla nearly or quite regular, 4-cleft: stamens 4, equal: flowers in heads or interrupted spikes, purplish or white. M. piperita, Linn. Peppermint. Straggling, 1-3 ft. tall, the plant dark colored (stems purplish): leaves ovate- oblong, or narrower, acute, sharply serrate: flowers light purple, in thick spikes 1-3 in. long. Europe. Cultivated and escaped. M. spicata, Linn. (M. viridis, Linn.). Spearmint. Fig. 481. Erect and smooth, 1-2 ft., green: leaves lanceolate and sharply serrate: flowers whitish or tinted, in long, in- terrupted spikes. Europe. Along roadsides, and cultivated. M, Canadénsis, Linn. Wild mint. One to 2 ft., pubes- cent: leaves lanceolate: flowers tinted, in whorls in the 484, Mentha spicata. axils of the leaves. Low grounds, 4. BRUNELLA. Sevr-neat. Low, usually unbranched perennials without aromatic odor: calyx about 10-nerved, 2-lipped: corolla 2-lipped, the upper lip arched and entire, the lower one 3-lobed: stamens 4, in pairs, ascending under the upper lip. B, vulgaris, Linn. Self-heal. Three to 10 in. tall, with ovate or oblong usually slightly toothed leaves: flowers small, violet (rarely white), in a dense, oblong, clover-like head or spike. Common in grassy places. 5. NEPETA. Carmint. Perennials, mostly sweet-scented: calyx nearly equally 5-toothed: co- rolla 2-lipped, the upper lip erect and somewhat concave, the lower 3-lobed: stamens 4, in pairs under the upper lip, the outer pair the shorter. N. Cataria, Linn. Common catmint or catnip. Fig. 197. Erect, 2-8 ft., pubescent: leaves cordate-ovate, crenate, grayish: corolla tinted: flowers in interrupted spikes, Introduced from Europe. 328 THE KINDS OF PLANTS 6. MARRUBIUM. Horenounp. Erect perennials, with white-woolly aspect: calyx nearly equally 5-10- toothed, the teeth very sharp: corolla 2-lipped, the upper lip erect and notched, the lower one spreading and 3-lobed: stamens 4, included in the corolla-tube. M. vulgare, Linn. Common horehound. Leaves broad-ovate and cre- nate: flowers small, white, in dense whorls. Europe, but common, 7. LEONURUS. Mornerwort. Erect perennials with green aspect: calyx about equally 5-toothed, the teeth becoming spine-like: corolla 2-lipped, the upper lip somewhat arched and entire, the lower spreading and 3-lobed: stamens 4, ascending under the upper lip: nutlets 3-angled. L. Cardiaca, Linn. Common motherwort. Tall: leaves rounded and lobed: corolla purple, the upper lip bearded: flowers in axillary whorls. Introduced from Europe. Common. XXI. CONVOLVULACEZ. Convotvunus Famity. Herbs, mostly twining, with alternate chiefly simple leaves: flowers regular, 5-merous, the tubular or trumpet-shaped corolla mostly twisted in the bud, the stamens 5 and borne on the corolla: ovary commonly 1-, mostly 2-loeuled, with 2 ovules in each loecule, becoming a globular capsule in fruit (which is sometimes 4-loculed by the insertion of a false partition). The family contains between 30 and 40 genera, and nearly 1,000 species. Common convolvulaceous plants are morning-glory, cypress vine, sweet potato, bindweed, dodder. AC Elan tsa wabhenonrnialleto liale eneretertetelatettctels st tetetelelheleieteitaste iterate 1. Ipomea AA. Plants leafless; parasitics. cj... 2c. «c/cls