THE STRUCTURE OF WOOD.

When it is remembered that the suitability of wood for a particular purpose depends most of all upon its internal structure, it is plain that the woodworker should know the essential characteristics of that structure. While his main interest in wood is as lumber, dead material to be used in woodworking, he can properly understand its structure only by knowing something of it as a live, growing organism. To facilitate this, a knowledge of its position in the plant world is helpful.

All the useful woods are to be found in the highest sub-kingdom of the plant world, the flowering plants or Phanerogamia of the botanist. These flowering plants are to be classified as follows:

Phanerogamia,
(Flowering plants)		 I. Gymnosperms. (Naked seeds.)
1. Cycadaceae. (Palms, ferns, etc.)
2. Gnetaceae. (Joint firs.)
3. Conifers. Pines, firs, etc.
II. Angiosperms. (Fruits.)
1. Monocotyledons. (One seed-leaf.)
(Palms, bamboos, grasses, etc.)
2. Dicotyledons. (Two seed-leaves.)
a. Herbs.
b. Broad-leaved trees.

Under the division of naked-seeded plants (gymnosperms), practically the only valuable timber-bearing plants are the needle-leaved trees or the conifers, including such trees as the pines, cedars, spruces, firs, etc. Their wood grows rapidly in concentric annual rings, like that of the broad-leaved trees; is easily worked, and is more widely used than the wood of any other class of trees.

Of fruit-bearing trees (angiosperms), there are two classes, those that have one seed-leaf as they germinate, and those that have two seed-leaves.

The one seed-leaf plants (monocotyledons) include the grasses, lilies, bananas, palms, etc. Of these there are only a few that reach the dimensions of trees. They are strikingly distinguished by the structure of their stems. They have no cambium layer and no distinct bark and pith; they have unbranched stems, which as a rule do not increase in diameter after the first stages of growth, but grow only terminally. Instead of having concentric annual rings and thus growing larger year by year, the woody tissue grows here and there thru the stem, but mostly crowded together toward the outer surfaces. Even where there is radial growth, as in yucca, the structure is not in annual rings, but irregular. These one seed-leaf trees (monocotyledons) are not of much economic value as lumber, being used chiefly "in the round," and to some extent for veneers and inlays; e. g., cocoanut-palm and porcupine wood are so used.

The most useful of the monocotyledons, or endogens, ("inside growers," as they are sometimes called,) are the bamboos, which are giant members of the group of grasses, Fig. 1. They grow in dense forests, some varieties often 70 feet high and 6 inches in diameter, shooting up their entire height in a single season. Bamboo is very highly valued in the Orient, where it is used for masts, for house rafters, and other building purposes, for gutters and water-pipes and in countless other ways. It is twice as strong as any of our woods.

Under the fruit-bearing trees (angiosperms), timber trees are chiefly found among those that have two seed-leaves (the dicotyledons) and include the great mass of broad-leaved or deciduous trees such as chestnut, oak, ash and maple. It is to these and to the conifers that our principal attention will be given, since they constitute the bulk of the wood in common use.

The timber-bearing trees, then, are the:

(1) Conifers, the needle-leaved, naked-seeded trees, such as pine, cedar, etc. Fig. 45, [p. 199].

(2) Endogens, which have one seed-leaf, such as bamboos, Fig. 1.

(3) Broad-leaved trees, having two seed-leaves, such as oak, beech, and elm. Fig. 48, [p. 203].

The common classifications of trees are quite inaccurate. Many of the so-called deciduous (Latin, deciduus, falling off) trees are evergreen, such as holly, and, in the south, live oak, magnolia and cherry. So, too, some of the alleged "evergreens," like bald cypress and tamarack, shed their leaves annually.

Fig. 1. A Bamboo Grove, Kioto, Japan.

Fig. 2. Ginko Leaf.

Not all of the "conifers" bear cones. For example, the juniper bears a berry. The ginko, Fig. 2, tho classed among the "conifers," the "evergreens," and the "needle-leaf" trees, bears no cones, has broad leaves and is deciduous. It has an especial interest as being the sole survivor of many species which grew abundantly in the carboniferous age.

Also, the terms used by lumbermen, "hard woods" for broad-leaved trees and "soft woods" for conifers, are still less exact, for the wood of some broad-leaved trees, as bass and poplar, is much softer than that of some conifers, as Georgia pine and lignum vitae.

Another classification commonly made is that of "endogens" (inside growers) including bamboos, palms, etc., and exogens (outside growers) which would include both conifers and broad-leaved trees.

One reason why so many classifications have come into use is that none of them is quite accurate. A better one will be explained later. See [p. 23].

As in the study of all woods three sections are made, it is well at the outset to understand clearly what these are.

The sections of a tree made for its study are (Fig. 3):

(1) Transverse, a plane at right angles to the organic axis.

(2) Radial, a longitudinal plane, including the organic axis.

Fig. 3.

A.B.
A, B, C, D, Transverse Section.
B, D, E, F, Radial Section.
G, H, I, J, Tangential Section.		 A, B, C, Transverse Section.
A, B, D, E, Radial Section.
B, C, E, F, Tangential Section.

(3) Tangential, a longitudinal plane not including the organic axis.

If a transverse section of the trunk of a conifer or of a broad-leaved tree is made, it is to be noted that it consists of several distinct parts. See Fig. 4. These, beginning at the outside, are:

Fig. 4. Diagram of Cross-section of Three Year Old Stem of Basswood.

(1) The rind or bark is made up of two layers, the outer of which, the "cortex," is corky and usually scales or pulls off easily; while the inner one is a fibrous coat called "bast" or "phloem." Together they form a cone, widest, thickest, and roughest at the base and becoming narrower toward the top of the tree. The cortex or outer bark serves to protect the stem of the tree from extremes of heat and cold, from atmospheric changes, and from the browsing of animals. It is made up of a tough water-proof layer of cork which has taken the place of the tender skin or "epidermis" of the twig. Because it is water-proof the outside tissue is cut off from the water supply of the tree, and so dries up and peels off, a mass of dead matter. The cork and the dead stuff together are called the bark. As we shall see later, the cork grows from the inside, being formed in the inner layers of the cortex, the outer layers of dry bark being thus successively cut off.

The characteristics of the tree bark are due to the positions and kinds of tissue of these new layers of cork. Each tree has its own kind of bark, and the bark of some is so characteristic as to make the tree easily recognizable.

Bark may be classified according to formation and method of separation, as scale bark, which detaches from the tree in plates, as in the willows; membraneous bark, which comes off in ribbons and films, as in the birches; fibrous bark, which is in the form of stiff threads, as in the grape vine; and fissured bark, which breaks up in longitudinal fissures, showing ridges, grooves and broad, angular patches, as in oak, chestnut and locust. The last is the commonest form of bark.

The bark of certain kinds of trees, as cherry and birch, has peculiar markings which consist of oblong raised spots or marks, especially on the young branches. These are called lenticels (Latin lenticula, freckle), and have two purposes: they admit air to the internal tissues, as it were for breathing, and they also emit water vapor. These lenticels are to be found on all trees, even where the bark is very thick, as old oaks and chestnuts, but in these the lenticels are in the bottoms of the deep cracks. There is a great difference in the inflammability of bark, some, like that of the big trees of California, Fig. 54, [p. 208], which is often two feet thick, being practically incombustible, and hence serving to protect the tree; while some bark, as canoe birch, is laden with an oil which burns furiously. It therefore makes admirable kindling for camp fires, even in wet weather.

Inside the cork is the "phloem" or "bast," which, by the way, gives its name to the bass tree, the inner bark of which is very tough and fibrous and therefore used for mat and rope making. In a living tree, the bast fibers serve to conduct the nourishment which has been made in the leaves down thru the stem to the growing parts.

(2) The cambium. Inside of the rind and between it and the wood, there is, on living trees, a slimy coat called cambium (Med. Latin, exchange). This is the living, growing part of the stem, familiar to all who have peeled it as the sticky, slimy coat between the bark and the wood of a twig. This is what constitutes the fragrant, mucilaginous inner part of the bark of slippery elm. Cambium is a tissue of young and growing cells, in which the new cells are formed, the inner ones forming the wood and the outer ones the bark.

Fig. 5. Young Stem, Magnified 18½ Diameters, Showing Primary and Secondary Bundles. By Courtesy of Mrs. Katharine Golden Bitting.

E, epidermis, the single outside layer of cells.

C, cortex, the region outside of the bundles.

HB, hard bast, the black, irregular ring protecting the soft bast.

SB, soft bast, the light, crescent-shaped parts.

Ca, cambium, the line between the soft bast and the wood.

W, wood, segments showing pores.

MR, medullary rays, lines between the bundles connecting the pith and the cortex.

MS, medullary sheath, the dark, irregular ring just inside the bundles.

P, pith, the central mass of cells.

In order to understand the cambium and its function, consider its appearance in a bud, Fig. 5. A cross-section of the bud of a growing stem examined under the microscope, looks like a delicate mesh of thin membrane, filled in with a viscid semi-fluid substance which is called "protoplasm" (Greek, protos, first; plasma, form). These meshes were first called "cells" by Robert Hooke, in 1667, because of their resemblance to the chambers of a honeycomb. The walls of these "cells" are their most prominent feature and, when first studied, were supposed to be the essential part; but later the slimy, colorless substance which filled the cells was found to be the essential part. This slimy substance, called protoplasm, constitutes the primal stuff of all living things. The cell walls themselves are formed from it. These young cells, at the apex of a stem, are all alike, very small, filled with protoplasm, and as yet, unaltered. They form embryonic tissue, i.e. one which will change. One change to which an cell filled with protoplasm is liable is division into two, a new partition wall forming within it. This is the way plant cells increase.

In young plant cells, the whole cavity of the chamber is filled with protoplasm, but as the cells grow older and larger, the protoplasm develops into different parts, one part forming the cell wall and in many cases leaving cavities within the cell, which become filled with sap. The substance of the cell wall is called cellulose (cotton and flax fibers consist of almost pure cellulose). At first it has no definite structure, but as growth goes on, it may become thickened in layers, or gummy, or hardened into lignin (wood), according to the function to be performed. Where there are a group of similar cells performing the same functions, the group is called a tissue or, if large enough, a tissue system.

When cells are changed into new forms, or "differentiated," as it is called, they become permanent tissues. These permanent tissues of the tree trunk constitute the various parts which we have noticed, viz., the rind, the pith and the wood.

The essentially living part of the tree, it should be remembered, is the protoplasm: where there is protoplasm, there is life and growth. In the stems of the conifers and broad-leaved trees—sometimes together called exogens—this protoplasm is to be found in the buds and in the cambium sheath, and these are the growing parts of the tree. If we followed up the sheath of cambium which envelopes a stem, into a terminal bud, we should find that it passed without break into the protoplasm of the bud.

In the cross-section of a young shoot, we might see around the central pith or medulla, a ring of wedge-shaped patches. These are really bundles of cells running longitudinally from the rudiments of leaves thru the stem to the roots. They are made of protoplasm and are called the "procambium strands," Fig. 6.

Fig. 6. Three Stages in the Development of an Exogenous Stem. P, pith; PB, primary bast; SB, secondary bast; C, cambium; PR, pith ray; PW, primary wood; SW, secondary wood; PS, procambium strands. After Boulger.

In the monocotyledons (endogens) these procambium strands change completely into wood and bast, and so losing all their protoplasmic cambium, become incapable of further growth. This is why palms can grow only lengthwise, or else by forming new fibers more densely in the central mass. But in the conifers and broad-leaved trees, the inner part of each strand becomes wood and the outer part bast (bark). Between these bundles, connecting the pith in the center with the cortex on the outside of the ring of bundles, are parts of the original pith tissue of the stem. They are the primary pith or medullary rays (Latin, medulla, pith). The number of medullary rays depends upon the number of the bundles; and their form, on the width of the bundles, so that they are often large and conspicuous, as in oak, or small and indeed invisible, as in some of the conifers. But they are present in all exogenous woods, and can readily be seen with the microscope. Stretching across these pith rays from the cambium layer in one procambium strand to that in the others, the cambium formation extends, making a complete cylindrical sheath from the bud downward over the whole stem. This is the cambium sheath and is the living, growing part of the stem from which is formed the wood on the inside and the rind (bark) on the outside.

In the first year the wood and the bast are formed directly by the growth and change of the inner and outer cells respectively of the procambium strand, and all such material is called "primary;" but in subsequent years all wood, pith rays, and bast, originate in the cambium, and these growths are called "secondary."

Fig. 7. Sap-wood and Heart-wood, Lignum Vitae.

(3) The wood of most exogens is made up of two parts, a lighter part called the sap-wood or splint-wood or alburnum, and a darker part called the heart-wood or duramen, Fig. 7. Sap-wood is really immature heartwood. The difference in color between them is very marked in some woods, as in lignum vitae and black walnut, and very slight in others, as spruce and bass. Indeed, some species never form a distinct heart-wood, birch (Betula alba) being an example.

In a living tree, sap-wood and heart-wood perform primarily quite different functions. The sap-wood carries the water from the roots to the leaves, stores away starch at least in winter, and in other ways assists the life of the tree. The proportional amount of sapwood varies greatly, often, as in long-leaf pine, constituting 40 per cent. of the stem.

As the sap-wood grows older, its cells become choked so that the sap can no longer flow thru them. It loses its protoplasm and starch and becomes heartwood, in which all cells are dead and serve only the mechanical function of holding up the great weight of the tree and in resisting wind pressures. This is the reason why a tree may become decayed and hollow and yet be alive and bear fruit. In a tree that is actually dead the sap-wood rots first.

Chemical substances infiltrate into the cell walls of heart-wood and hence it has a darker color than the sap-wood. Persimmon turns black, walnut purplish brown, sumac yellow, oak light brown, tulip and poplar yellowish, redwood and cedar brownish red. Many woods, as mahogany and oak, darken under exposure, which shows that the substances producing the color are oxidizable and unstable. Wood dyes are obtained by boiling and distilling such woods as sumach, logwood, red sanders, and fustic. Many woods also acquire distinct odors, as camphor, sandalwood, cedar, cypress, pine and mahogany, indicating the presence of oil.

As a rule heart-wood is more valuable for timber, being harder, heavier, and drier than sap-wood. In woods like hickory and ash, however, which are used for purposes that require pliability, as in baskets, or elasticity as in handles of rakes and hoes, sap-wood is more valuable than heart-wood.

In a transverse section of a conifer, for example Douglas spruce, Fig. 8, the wood is seen to lie in concentric rings, the outer part of the ring being darker in color than the inner part. In reality each of these rings is a section of an irregular hollow cone, each cone enveloping its inner neighbor. Each cone ordinarily constitutes a year's growth, and therefore there is a greater number of them at the base of a tree than higher up. These cones vary greatly in thickness, or, looking at a cross-section, the rings vary in width; in general, those at the center being thicker than those toward the bark. Variations from year to year may also be noticed, showing that the tree was well nourished one year and poorly nourished another year. Rings, however, do not always indicate a year's growth. "False rings" are sometimes formed by a cessation in the growth due to drouth, fire or other accident, followed by renewed growth the same season.

Fig. 8. Section of Douglas Fir, Showing Annual Rings and Knots at Center of Trunk. American Museum of Natural History, N. Y.

In a radial section of a log, Fig. 8, these "rings" appear as a series of parallel lines and if one could examine a long enough log these lines would converge, as would the cut edges in a nest of cones, if they were cut up thru the center, as in Fig. 9.

Fig. 9. Diagram of Radial Section of Log (exaggerated) Showing Annual Cones of Growth.

In a tangential section, the lines appear as broad bands, and since almost no tree grows perfectly straight, these lines are wavy, and give the characteristic pleasing "grain" of wood. Fig. 27, [p. 35]. The annual rings can sometimes be discerned in the bark as well as in the wood, as in corks, which are made of the outer bark of the cork oak, a product of southern Europe and northern Africa. Fig. 10.

Fig. 10. Annual Rings in Bark (cork).

The growth of the wood of exogenous trees takes place thru the ability, already noted, of protoplasmic cells to divide. The cambium cells, which have very thin walls, are rectangular in shape, broader tangentially than radially, and tapering above and below to a chisel edge, Fig. 11. After they have grown somewhat radially, partition walls form across them in the longitudinal, tangential direction, so that in place of one initial cell, there are two daughter cells radially disposed. Each of these small cells grows and re-divides, as in Fig. 12. Finally the innermost cell ceases to divide, and uses its protoplasm to become thick and hard wood. In like manner the outermost cambium cell becomes bast, while the cells between them continue to grow and divide, and so the process goes on. In nearly all stems, there is much more abundant formation of wood than of bast cells. In other words, more cambium cells turn to wood than to bast.

Fig. 11. Diagram Showing Grain of Spruce Highly Magnified. PR, pith rays; BP, bordered pits; Sp W, spring wood; SW, summer wood; CC, overlapping of chisel shaped ends.

Fig. 12. Diagram Showing the Mode of Division of the Cambium Cells. The cambium cell is shaded to distinguish it from the cells derived from it. Note in the last division at the right that the inner daughter cell becomes the cambium cell while the outer cell develops into a bast cell. From Curtis: Nature and Development of Plants.

In the spring when there is comparatively little light and heat, when the roots and leaves are inactive and feeble, and when the bark, split by winter, does not bind very tightly, the inner cambium cells produce radially wide wood cells with relatively thin walls. These constitute the spring wood. But in summer the jacket of bark binds tightly, there is plenty of heat and light, and the leaves and roots are very active, so that the cambium cells produce thicker walled cells, called summer wood. During the winter the trees rest, and no development takes place until spring, when the large thin-walled cells are formed again, making a sharp contrast with those formed at the end of the previous season.

It is only at the tips of the branches that the cambium cells grow much in length; so that if a nail were driven into a tree twenty years old at, say, four feet from the ground, it would still be four feet from the ground one hundred years later.

Looking once more at the cross-section, say, of spruce, the inner portion of each ring is lighter in color and softer in texture than the outer portion. On a radial or tangential section, one's finger nail can easily indent the inner portion of the ring, tho the outer dark part of the ring may be very hard. The inner, light, soft portion of the ring is the part that grows in the spring and early summer, and is called the "spring wood" while the part that grows later in the season is called "summer wood." As the summer wood is hard and heavy, it largely determines the strength and weight of the wood, so that as a rule, the greater the proportion of the summer growth, the better the wood. This can be controlled to some extent by proper forestry methods, as is done in European larch forests, by "underplanting" them with beech.

In a normal tree, the summer growth forms a greater proportion of the wood formed during the period of thriftiest growth, so that in neither youth nor old age, is there so great a proportion of summer wood as in middle age.

It will help to make clear the general structure of wood if one imagines the trunk of a tree to consist of a bundle of rubber tubes crushed together, so that they assume angular shapes and have no spaces between them. If the tubes are laid in concentric layers, first a layer which has thin walls, then successive layers having thicker and thicker walls, then suddenly a layer of thin-walled tubes and increasing again to thick-walled ones and so on, such an arrangement would represent the successive annual "rings" of conifers.

The medullary rays. While most of the elements in wood run longitudinally in the log, it is also to be noted that running at right angles to these and radially to the log, are other groups of cells called pith rays or medullary rays (Latin, medulla, which means pith). These are the large "silver flakes" to be seen in quartered oak, which give it its beautiful and distinctive grain, Fig. 32, [p. 37]. They appear as long, grayish lines on a cross-section, as broad, shining bands on the radial section, and as short, thick lines tapering at each end on the tangential section. In other words, they are like flat, rectangular plates standing on edge and radiating lengthwise from the center of the tree. They vary greatly in size in different woods. In sycamore they are very prominent, Fig. 13. In oak they are often several hundred cells wide (i.e., up and down in the tree). This may amount to an inch or two. They are often twenty cells thick, tapering to one cell at the edge. In oak very many are also small, even microscopic. But in the conifers and also in some of the broad-leaved trees, altho they can be discerned with the naked eye on a split radial surface, still they are all very small. In pine there are some 15,000 of them to a square inch of a tangential section. They are to be found in all exogens. In a cross-section, say of oak, Fig. 14, it can readily be seen that some pith rays begin at the center of the tree and some farther out. Those that start from the pith are formed the first year and are called primary pith rays, while those that begin in a subsequent year, starting at the cambium of that year, are called secondary rays.

Fig. 13. Tangential Section of Sycamore, Magnified 37 Diameters. Note the large size of the pith rays, A, A (end view).

The function of the pith rays is twofold. (1) They transfer formative material from one part of a stem to another, communicating with both wood and bark by means of the simple and bordered pits in them, and (2) they bind the trunk together from pith to bark. On the other hand their presence makes it easier for the wood to split radially.

The substance of which they are composed is "parenchyma" (Greek, beside, to pour), which also constitutes the pith, the rays forming a sort of connecting link between the first and last growth of the tree, as the cambium cells form new wood each year.

Fig. 14 Cross-section of White Oak. The Radiating White Lines are the Pith Rays.

If a cambium cell is opposite to a pith ray, it divides crosswise (transversely) into eight or ten cells one above another, which stretch out radially, retaining their protoplasm, and so continue the pith ray. As the tree grows larger, new, or secondary medullary rays start from the cambium then active, so that every year new rays are formed both thinner and shorter than the primary rays, Fig. 14.

Now suppose that laid among the ordinary thin-walled tubes were quite large tubes, so that one could tell the "ring" not only by the thin walls but by the presence of large tubes. That would represent the ring-porous woods, and the large tubes would be called vessels, or tracheæ. Suppose again that these large tubes were scattered in disorder thru the layers. This arrangement would represent the diffuse-porous woods.

By holding up to the light, thin cross-sections of spruce or pine, Fig. 15, oak or ash, Fig. 16, and bass or maple, Fig. 17, these three quite distinct arrangements in the structure may be distinguished. This fact has led to the classification of woods according to the presence and distribution of "pores," or as they are technically called, "vessels" or "tracheae." By this classification we have:

(1) Non-porous woods, which comprise the conifers, as pine and spruce.

(2) Ring-porous woods, in which the pores appear (in a cross-section) in concentric rings, as in chestnut, ash and elm.

(3) Diffuse-porous woods, in which (in a cross-section) the rings are scattered irregularly thru the wood, as in bass, maple and yellow poplar.

In order to fully understand the structure of wood, it is necessary to examine it still more closely thru the microscope, and since the three classes of wood, non-porous, ring-porous and diffuse-porous, differ considerably in their minute structure, it is well to consider them separately, taking the simplest first.

Fig. 15. Cross-section of Non-porous Wood, White Pine, Full Size (top toward pith).

Non-porous woods. In examining thru the microscope a transverse section of white pine, Fig. 18:

(1) The most noticeable characteristic is the regularity of arrangement of the cells. They are roughly rectangular and arranged in ranks and files.

(2) Another noticeable feature is that they are arranged in belts, the thickness of their walls gradually increasing as the size of the cells diminishes. Then the large thin-walled cells suddenly begin again, and so on. The width of one of these belts is the amount of a single year's growth, the thin-walled cells being those that formed in spring, and the thick-walled ones those that formed in summer, the darker color of the summer wood as well as its greater strength being caused by there being more material in the same volume.

Fig. 16. Cross-section of Ring-porous Wood, White Ash, Full Size (top toward pith).

Fig. 17. Cross-section of Diffuse-porous Wood, Hard Maple, full size (top toward pith).

(3) Running radially (up and down in the picture) directly thru the annual belts or rings are to be seen what looks like fibers. These are the pith or medullary rays. They serve to transfer formative material from one part of the stem to another and to bind the tree together from pith to bark.

(4) Scattered here and there among the regular cells, are to be seen irregular gray or yellow dots which disturb the regularity of the arrangement. These are resin ducts. (See cross-section of white pine, Fig. 18.) They are not cells, but openings between cells, in which the resin, an excretion of the tree, accumulates, oozing out when the tree is injured. At least one function of resin is to protect the tree from attacks of fungi.

Looking now at the radial section, Fig. 18:

(5) The first thing to notice is the straightness of the long cells and their overlapping where they meet endwise, like the ends of two chisels laid together, Fig. 11.

(6) On the walls of the cells can be seen round spots called "pits." These are due to the fact that as the cell grows, the cell walls thicken, except in these small spots, where the walls remain thin and delicate. The pit in a cell wall always coincides with the pit in an adjoining cell, there being only a thin membrane between, so that there is practically free communication of fluids between the two cells. In a cross-section the pit appears as a canal, the length of which depends upon the thickness of the walls. In some cells, the thickening around the pits becomes elevated, forming a border, perforated in the center. Such pits are called bordered pits. These pits, both simple and bordered, are waterways between the different cells. They are helps in carrying the sap up the tree.

(7) The pith rays are also to be seen running across and interwoven in the other cells. It is to be noticed that they consist of several cells, one above another.

In the tangential section, Fig. 18:

(8) The straightness and overlapping of the cells is to be seen again, and

(9) The numerous ends of the pith rays appear.

In a word, the structure of coniferous wood is very regular and simple, consisting mainly of cells of one sort, the pith rays being comparatively unnoticeable. This uniformity is what makes the wood of conifers technically valuable.

Fig. 18.

Fig. 19. Isolated Fibers and Cells. a, four cells of wood parenchyma; b, two cells from a pith ray; c, a single cell or joint of a vessel, the openings, x, x, leading into its upper and lower neighbors; d, tracheid; e, wood fiber proper. After Roth.

The cells of conifers are called tracheids, meaning "like tracheæ." They are cells in which the end walls persist, that is, are not absorbed and broken down when they meet end to end. In other words, conifers do not have continuous pores or vessels or "tracheæ," and hence are called "non-porous" woods.

But in other woods, the ends of some cells which meet endwise are absorbed, thus forming a continuous series of elements which constitute an open tube. Such tubes are known as pores, or vessels, or "tracheæ," and sometimes extend thru the whole stem. Besides this marked difference between the porous and non-porous woods, the porous woods are also distinguished by the fact that instead of being made up, like the conifers of cells of practically only one kind, namely tracheids, they are composed of several varieties of cells. Besides the tracheae and tracheids already noted are such cells as "wood fiber," "fibrous cells," and "parenchyma." Fig. 19. Wood fiber proper has much thickened lignified walls and no pits, and its main function is mechanical support. Fibrous cells are like the wood fibers except that they retain their protoplasm. Parenchyma is composed of vertical groups of short cells, the end ones of each group tapering to a point, and each group originates from the transverse division of one cambium cell. They are commonly grouped around the vessels (tracheæ). Parenchyma constitutes the pith rays and other similar fibers, retains its protoplasm, and becomes filled with starch in autumn.

The most common type of structure among the broad-leaved trees contains tracheæ, trachæids, woody fiber, fibrous cells and parenchyma. Examples are poplars, birch, walnut, linden and locust. In some, as ash, the tracheids are wanting; apple and maple have no woody fiber, and oak and plum no fibrous cells.

This recital is enough to show that the wood of the broad-leaved trees is much more complex in structure than that of the conifers. It is by means of the number and distribution of these elements that particular woods are identified microscopically. See [p. 289].

Fig. 20.

Ring-porous woods. Looking thru the microscope at a cross-section of ash, a ring-porous wood, Fig. 20:

Looking at the radial section, Fig. 20:

In the tangential section, Fig. 20:

In diffuse porous woods, the main features to be noticed are: In the transverse section, Fig. 21:

In the radial section, Fig. 21:

In the tangential section, Fig. 21:

Fig. 21.